BGD Tutorial - Applied Embryology and Teratology: Difference between revisions

From Embryology
mNo edit summary
mNo edit summary
(104 intermediate revisions by the same user not shown)
Line 1: Line 1:
{{Header}}
{{Header}}
== Introduction ==
== Introduction ==


Line 8: Line 9:




      Tinycc page - http://tiny.cc/BGD2_Tutorial


Similar content was covered in the previous online tutorials in [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=237949 2016] | [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=205145 2015] | [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=139716 2014] | [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=117268 2012] | [[Media:BGD Tutorial 2015 - Applied Embryology and Teratology.pdf|2015 PDF]] | [[Media:BGD Tutorial 2014 - Applied Embryology and Teratology.pdf|2014 PDF]] |  [[Media:BGD Tutorial 2012- Applied Embryology and Teratology Embryology.pdf|2012 PDF]] | [[Media:BGD Tutorial 2011- Applied Embryology and Teratology Embryology.pdf|2011 PDF]] and [[2010 BGD Tutorial - Applied Embryology and Teratology|2010]].
 
Similar content was covered in the previous online tutorials in  
 
[https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=359971 2018] | [[Media:2018 BGD Tutorial - Applied Embryology and Teratology.pdf|2018 PDF]] | [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=295069 2017] | [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=237949 2016] | [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=205145 2015] | [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=139716 2014] | [https://embryology.med.unsw.edu.au/embryology/index.php?title=BGD_Tutorial_-_Applied_Embryology_and_Teratology&oldid=117268 2012] | [[Media:BGD Tutorial 2015 - Applied Embryology and Teratology.pdf|2015 PDF]] | [[Media:BGD Tutorial 2014 - Applied Embryology and Teratology.pdf|2014 PDF]] |  [[Media:BGD Tutorial 2012- Applied Embryology and Teratology Embryology.pdf|2012 PDF]] | [[Media:BGD Tutorial 2011- Applied Embryology and Teratology Embryology.pdf|2011 PDF]] and [[2010 BGD Tutorial - Applied Embryology and Teratology|2010]].


{| class="wikitable mw-collapsible mw-collapsed"
{| class="wikitable mw-collapsible mw-collapsed"
! Whats in the News?  
! Whats in the News?  
|-bgcolor="F5FAFF"
|-
|  
|  
{{Main Page News}}
[[File:Australian maternal physical activity 2011-2012.jpg|thumb|alt=Australian maternal physical activity 2011-2012|Australian maternal physical activity 2011-2012]]
|-
* This report looks at the types and amount of physical activity undertaken by women during pregnancy using the Australian Bureau of Statistics’ Australian Health Survey 2011–12. It compares activity levels for pregnant and non-pregnant women of the same ages and assesses these levels against the Australian physical activity guideline for adults.<ref name=AIHW-2011-2012_Physical_Activity>{{Ref-AIHW-2011–2012_Physical_activity_pregnancy2019}}</ref>
| [[Australian_Statistics#National_Core_Maternity_Indicators_stage_3_and_4_results_from_2010.E2.80.932013|National Core Maternity Indicators stage 3 and 4 results from 2010–2013]] (19 Jul 2016)
** Only 3 in 10 pregnant women met the physical activity guideline
|-
** Two-thirds of pregnant women were active for fewer than 150 minutes per week
| [[File:Monitoring the health impacts of mandatory folic acid and iodine fortification 2016.jpg|150px|right|alt=AIHW Report - Folic acid and iodine fortification (2016)]] Folic acid and iodine fortification (2016)<ref name=“PHE208”>AIHW 2016. '''Monitoring the health impacts of mandatory folic acid and iodine fortification 2016'''. [http://www.aihw.gov.au/publication-detail/?id=60129555435 Cat. no. '''PHE 208''']. Canberra: AIHW. [http://www.aihw.gov.au/WorkArea/DownloadAsset.aspx?id=60129555568 PDF]</ref>
** Just over half of pregnant women exercised for fitness, usually walking
[[File:Endocrine disrupting chemicals historical timeline.jpg|thumb|alt=Endocrine disrupting chemicals historical timeline|Endocrine disrupting chemicals historical timeline{{#pmid:30881345|PMID30881345}}]]
* '''Endocrine Disrupting Chemicals: An Occult Mediator of Metabolic Disease'''{{#pmid:30881345|PMID30881345}} "Endocrine disrupting {{chemicals}} (EDCs), a heterogeneous group of exogenous chemicals that can interfere with any aspect of endogenous hormones, represent an emerging global threat for human metabolism. There is now considerable evidence that the observed upsurge of metabolic disease cannot be fully attributed to increased caloric intake, physical inactivity, sleep deficit, and ageing. Among environmental factors implicated in the global deterioration of metabolic health, EDCs have drawn the biggest attention of scientific community, and not unjustifiably. EDCs unleash a coordinated attack toward multiple components of human metabolism, including crucial, metabolically-active organs such as hypothalamus, adipose tissue, pancreatic beta cells, skeletal muscle, and liver. Specifically, EDCs' impact during critical developmental windows can promote the disruption of individual or multiple systems involved in metabolism, via inducing epigenetic changes that can permanently alter the epigenome in the germline, enabling changes to be transmitted to the subsequent generations. The clear effect of this multifaceted attack is the manifestation of metabolic disease, clinically expressed as obesity, metabolic syndrome, diabetes mellitus, and non-alcoholic fatty liver disease."


* '''Maternal Vaccination''' - The Safety of Influenza and Pertussis Vaccination in Pregnancy in a Cohort of Australian Mother-Infant Pairs, 2012-2015: The FluMum Study{{#pmid:30475988|PMID30475988}} "Inactivated influenza vaccine (IIV) and pertussis vaccination are recommended in pregnancy. Limited safety data exist for women who received IIV vaccine during the first trimester of pregnancy or received both vaccines in pregnancy. We assessed adverse birth outcomes between vaccinated and unvaccinated pregnancies. METHODS: Among prospectively enrolled Australian "FluMum" participants (2012-2015), primary exposure was receipt and timing of IIV during pregnancy. Primary outcomes included preterm birth, low birthweight at term (LBWT), and small for gestational age (SGA). We compared birth outcomes for IIV in pregnancy with women unvaccinated in pregnancy using Cox proportional hazard ratios (HRs) with 95% confidence intervals (CIs). ...No significant associations were found between maternal IIV or pertussis vaccination in pregnancy and adverse birth outcomes, regardless of the trimester of pregnancy a vaccination was given compared to unvaccinated pregnancies."
** '''(No) Association between seasonal influenza vaccination with pre- and postnatal outcomes'''{{#pmid:30799158|PMID30799158}} "This study found no evidence of adverse maternal and infant outcomes associated with seasonal influenza vaccine during pregnancy. On the contrary, vaccinated women were less likely to have adverse outcomes than unvaccinated women. The lack of increased adverse outcomes associated with influenza vaccination suggests that the benefits of vaccination during pregnancy to the woman and her child far outweigh any risk, if there is one, from the vaccination."


* Mandatory fortification of bread with folic acid (in Australia) and iodine (in Australia and New Zealand) was introduced in 2009
* '''Gastroenteritis''' - Perinatal Risk Factors Associated With Gastroenteritis Hospitalizations in Aboriginal and Non-Aboriginal Children in Western Australia (2000-2012): A Record Linkage Cohort Study{{#pmid:29620723|PMID29620723}} "Gastroenteritis is a leading cause of childhood morbidity worldwide. We aimed to assess the maternal and infant characteristics and population attributable fractions associated with childhood gastroenteritis-related hospitalizations. METHODS: We conducted a whole-of-population retrospective birth cohort study of 367,476 children live-born in Western Australia 2000-2012.  ...Given the beneficial effect of infant rotavirus vaccination in preventing all-cause gastroenteritis hospitalization, efforts should be taken to optimize rotavirus vaccine coverage in those at highest risk."
* Overall decrease in the rate of neural tube defects (NTDs) by 14.4%
* Teenagers the rate of NTDs decreased by almost 55%
* Aboriginal and Torres Strait Islander women the rate of NTDs decreased by 74%


:'''Links:''' [[Abnormal Development - Folic Acid and Neural Tube Defects|Folic Acid and Neural Tube Defects]] | [[Abnormal Development - Iodine Deficiency|Iodine Deficiency]] | [[Australian Statistics]] | [http://www.aihw.gov.au/food-and-nutrition/folic-acid-and-iodine AIHW - folic acid and iodine]
* '''intrauterine Growth Restriction''' Human papillomavirus infection and intrauterine growth restriction: a data-linkage study{{#pmid:28889772|PMID28889772}} "Using unbiased population data, to examine whether having a positive Pap smear, and thus a high probability of Human Papilloma Virus (HPV) infection, is a significant risk factor for intrauterine growth restriction (IUGR) in a subsequent pregnancy. CONCLUSIONS: Mothers with a positive Pap smear have an increased risk of IUGR, especially for VLBW, which is independent of other risk factors. The results confirm previous findings in a small study and emphasise the need to consider the risks of both cancer and IUGR in all HPV vaccination programs."
|-
|-
! ZIKA Virus
| [[File:Pregnancy-care-guidelines-5Feb18-1.jpg|thumb|150px|Pregnancy Care Guidelines 2018]]
|-
 
| [[File:Zika virus world map.jpg|300px|Zika virus world map (CDC 2016)]][[File:Mosquito lifecycle.jpg|300px|alt=Mosquito lifecycle]]
* 8 October 2018 -  [https://beta.health.gov.au/resources/publications/pregnancy-care-guidelines Online Update]
|-
* [http://www.health.gov.au/internet/main/publishing.nsf/Content/pregnancycareguidelines Clinical Practice Guidelines - Pregnancy Care Guidelines] released 5 Feb 2018.<ref name=PregnancyCare2018>{{Ref-PregnancyCare2018}}</ref>
| Zika virus (ZIKV) is a mosquito-borne ''flavivirus'' related to dengue virus first isolated from a rhesus monkey in Zika forest, Uganda (1947). Transmitted by mosquitoes (''Aedes aegypti'') it was then identified in humans in Nigeria in 1954 and subsequently in South America, Asia and Pacific regions. More recently in Australia from returning travellers.<ref><pubmed>24944843</pubmed></ref>  Mosquito bites lead to an initial infection of skin cells.<ref><pubmed>26085147</pubmed></ref> The virus may also be transmitted transplacentally or during delivery.<ref><pubmed>24721538</pubmed></ref> Some limited evidence, from Brazil, for association with microcephaly. (More? [[Abnormal Development - Zika Virus]] | [[Abnormal Development - Viral Infection]])
|-
! Pertussis (whooping cough) Increase
|-
| [[File:NSW-pertussis-notification-graph 2012-16.jpg|left|300px]]There has been a recent significant increase in the total number of pertussis (whooping cough) notifications in NSW, Australia.


This edition brings together the two previous modules and contains updates of a number of topics from them, including weight and body mass index (weight monitoring reviewed), fetal growth and wellbeing, risk of {{preterm birth}}, risk of pre-eclampsia (risk factors and prediction reviewed), family violence, hyperglycaemia (early testing reviewed), hepatitis C, thyroid dysfunction, vitamin D status and chromosomal anomalies (cell- free DNA testing reviewed). The new topic substance use has also been incorporated.


Pertussis (whooping cough, 100-day cough) is a highly contagious bacterial (Bordetella pertussis) infection prevented by vaccination with the pertussis vaccine. Symptoms are initially similar to the common cold. Neonatal infection can be fatal, with 1% of infected infants under one year of age dying, other complications include: pneumonia (lung infection), convulsions (violent, uncontrolled shaking), apnea (slowed or stopped breathing) and encephalopathy (disease of the brain). (More? [[Postnatal - Infectious Diseases School Exclusion]] | [[Neonatal Development]] | [[Abnormal Development - Bacterial Infection]])
See also {{Ref-Australian Immunisation Handbook2015}}.<br>
[[File:Aus-Imm-Handbook-2015.jpg|150px|link=Postnatal - Vaccination]]
|-
|  
{{Main Page News}}
|-
|-
| [[File:Pituitary thyroid pathway.jpg|left|200px]]'''Association of maternal thyroid function during early pregnancy with offspring IQ and brain morphology in childhood''' PMID 26497402


* Maternal levels of free T4 during pregnancy correlate with their offspring's IQ, cortex volume and grey matter volume
* Both the upper and lower limits of normal maternal levels of free T4 during pregnancy are associated with reduced child IQ, as well as decreased child cortex and grey matter volume
• Maternal levels of TSH during pregnancy are not associated with child IQ or child brain morphology
|}
|}


Line 82: Line 84:


== Applied Embryology ==
== Applied Embryology ==
[[File:Australia's mothers and babies 2014.jpg|link=Australia’s_mothers_and_babies_2014|thumb|Australia’s mothers and babies - in brief 2014 (published 2016).]]
[[File:Australia's mothers and babies 2016.jpg|link=Australia’s_mothers_and_babies_2016|thumb|Australia’s mothers and babies - in brief 2016 (published 2018).<ref name=AMB16>{{Ref-AMB2016}}</ref>]]  


The information is based upon data from the most recent 2016 publication "Australia's mothers and babies 2014 - in brief"<ref name=AMB2014>AIHW 2016. Australia's mothers and babies 2014—in brief. Perinatal statistics series no. 32. [ http://www.aihw.gov.au/publication-detail/?id=60129557656 Cat. no. PER 87]. Canberra: AIHW.</ref> and earlier reports.<ref name="AMB2015">AIHW 2015. [[Australia’s_mothers_and_babies_2013|Australia's mothers and babies 2013 - in brief]]. Perinatal statistics series no. 31. Cat. no. PER 72. Canberra: AIHW. [http://www.aihw.gov.au/WorkArea/DownloadAsset.aspx?id=60129554140 PDF] Viewed 13 December 2015. http://www.aihw.gov.au/publication-detail/?id=60129553770</ref><ref>Hilder L, Zhichao Z, Parker M, Jahan S, Chambers GM 2014. '''Australia’s mothers and babies 2012.''' Perinatal statistics series no. 30. Cat. no. PER 69. Canberra: AIHW. Viewed 16 December 2014. http://www.aihw.gov.au/publication-detail/?id=60129550033</ref><ref>Li Z, Zeki R, Hilder L & Sullivan EA 2013. [[Australia’s_mothers_and_babies_2011|'''Australia’s mothers and babies 2011''']]. Perinatal statistics series no. 28. Cat. no. PER 59. Canberra: AIHW.</ref><ref>Li Z, McNally L, Hilder L & Sullivan EA 2011. [[Australia’s_mothers_and_babies_2009|'''Australia's mothers and babies 2009''']] [http://www.aihw.gov.au/publication-detail/?id=10737420870 AIHW Perinatal statistics series no. 25] Cat. no. PER 52. Sydney: AIHW National Perinatal Epidemiology and Statistics Unit.</ref><ref>Laws P & Sullivan EA 2010  [[Australia’s_mothers_and_babies_2008|'''Australia's mothers and babies 2008''']] [http://www.aihw.gov.au/publications/index.cfm/title/11813 AIHW Perinatal statistics series no. 24] Cat. no. PER 48. Sydney: AIHW National Perinatal Statistics Unit.</ref><ref>Laws P & Sullivan EA 2009. [[Australia’s_mothers_and_babies_2007|'''Australia's mothers and babies 2007''']] [http://www.aihw.gov.au/publications/index.cfm/title/10972 AIHW Perinatal statistics series no. 23] Cat. no. PER 48. Sydney: AIHW National Perinatal Statistics Unit.</ref>
 
The data below is based the 2015 data<ref name=AMB15>{{Ref-AMB2015}}</ref> and will be updated to the more recent 2016 data (published 2018). Earlier report data summaries are also available.<ref name=AMB2014>AIHW 2016. Australia's mothers and babies 2014—in brief. Perinatal statistics series no. 32. [ http://www.aihw.gov.au/publication-detail/?id=60129557656 Cat. no. PER 87]. Canberra: AIHW.</ref><ref name="AMB2015">AIHW 2015. [[Australia’s_mothers_and_babies_2013|Australia's mothers and babies 2013 - in brief]]. Perinatal statistics series no. 31. Cat. no. PER 72. Canberra: AIHW. [http://www.aihw.gov.au/WorkArea/DownloadAsset.aspx?id=60129554140 PDF] Viewed 13 December 2015. http://www.aihw.gov.au/publication-detail/?id=60129553770</ref><ref>Hilder L, Zhichao Z, Parker M, Jahan S, Chambers GM 2014. '''Australia’s mothers and babies 2012.''' Perinatal statistics series no. 30. Cat. no. PER 69. Canberra: AIHW. Viewed 16 December 2014. http://www.aihw.gov.au/publication-detail/?id=60129550033</ref><ref>Li Z, Zeki R, Hilder L & Sullivan EA 2013. [[Australia’s_mothers_and_babies_2011|'''Australia’s mothers and babies 2011''']]. Perinatal statistics series no. 28. Cat. no. PER 59. Canberra: AIHW.</ref><ref>Li Z, McNally L, Hilder L & Sullivan EA 2011. [[Australia’s_mothers_and_babies_2009|'''Australia's mothers and babies 2009''']] [http://www.aihw.gov.au/publication-detail/?id=10737420870 AIHW Perinatal statistics series no. 25] Cat. no. PER 52. Sydney: AIHW National Perinatal Epidemiology and Statistics Unit.</ref><ref>Laws P & Sullivan EA 2010  [[Australia’s_mothers_and_babies_2008|'''Australia's mothers and babies 2008''']] [http://www.aihw.gov.au/publications/index.cfm/title/11813 AIHW Perinatal statistics series no. 24] Cat. no. PER 48. Sydney: AIHW National Perinatal Statistics Unit.</ref><ref>Laws P & Sullivan EA 2009. [[Australia’s_mothers_and_babies_2007|'''Australia's mothers and babies 2007''']] [http://www.aihw.gov.au/publications/index.cfm/title/10972 AIHW Perinatal statistics series no. 23] Cat. no. PER 48. Sydney: AIHW National Perinatal Statistics Unit.</ref>


This data should help you as a clinician and researcher to understand the current trends in reproductive medicine within Australia. Also see recent general population data in [[Australian Statistics]].
This data should help you as a clinician and researcher to understand the current trends in reproductive medicine within Australia. Also see recent general population data in [[Australian Statistics]].
{|
{|
|  
|  
* '''2013''' - 307,277 live births and 2,191 stillbirths
* '''2015''' - 306,725 live births and 2,160 (less than 1%) were {{stillbirth}}
* '''2012''' - 312,153 live births and 2,255 fetal deaths
* '''2014''' - 307,844 live births and 2,200
* '''2011''' - 301,810 live births and 2,220 fetal deaths
* '''2013''' - 307,277 live births and 2,191  
* '''2009''' - 296,791 live births and 2,341 fetal deaths
* '''2012''' - 312,153 live births and 2,255  
* '''2008''' - 294,737 live births and 2,188 fetal deaths
* '''2011''' - 301,810 live births and 2,220  
* '''2007''' - 292,027 live births and 2,177 fetal deaths
* '''2009''' - 296,791 live births and 2,341
* '''2008''' - 294,737 live births and 2,188  
* '''2007''' - 292,027 live births and 2,177
 
* Congenital abnormalities are the leading cause of perinatal deaths (fetal+neonatal)
| [[File:Australian-births_2011.jpg|400px]]
| [[File:Australian-births_2011.jpg|400px]]
|}
|}
==Mothers==
==Mothers==
{| class="wikitable mw-collapsible mw-collapsed"
{| class="wikitable mw-collapsible mw-collapsed"
! Mothers
! Mothers - 2015 &nbsp;
|-
|-
|  
|  
*  In 2014, 307,844 women gave birth in Australia—an increase of 18% since 2004 (252,871)
'''304,268''' women gave birth in Australia — an increase of 13% since 2005 (267,795 women).
* Rate of women giving birth increased from '''59''' per 1,000 women of reproductive age (15–44 years) in 2004 to '''63''' per 1,000 in 2014.
* Average age of all women who gave birth continues to rise and was [[Genetic_risk_maternal_age|'''30.2''']] in 2014 (30.1 2013)
* Proportion of mothers aged 35 and over increased from 20% in 2004 to 22% in 2014.
* Proportion of mothers aged under 25 has decreased from 19% to 16%.
* 98% (300,282) of women gave birth in hospitals
* 205,927 of women (67%) had a vaginal birth and 101,896 (33%) had a caesarean section.
|-
| Maternal Conditions
* One in 9 women (33,280 or 11%) who gave birth in 2014 smoked at some time during their pregnancy, a decrease from 15% in 2009.
* 8 per 1,000 mothers had chronic hypertension and 34 per 1,000 had gestational hypertension;
* 10 per 1,000 had pre‐existing diabetes and 83 per 1,000 had gestational diabetes.
|}


{| class="wikitable mw-collapsible mw-collapsed"
Rate of women giving birth 62 per 1,000 women of reproductive age (15–44 years)
! Mothers 2013
* rate has declined from a peak of 66 per 1,000 women in 2007.
|-
* rate has fluctuated between 2005 and 2015
|
* Average maternal age in 2013 was  [[Genetic_risk_maternal_age|'''30.1''']] years, more than the earlier years (2011, 30.0 years; 2000, 29.0 years; 2002, 29.4 years).
* Approximately '''43.0%''' (2009, 41.6%) of women were having their first baby.
** Average age for first time mothers was 28.6 (27.8 years in 2003).  
* mothers aged 35 and over has increased from 19% in 2003 to 22% in 2013, (mothers aged less than 24 has decreased from 19% to 17%).


[[Genetic risk maternal age|Average age]] of all women who gave birth continues to rise and was [[Genetic risk maternal age|'''30.3''']], compared with 29.7 in 2005.
* The median age was slightly higher, at 31 years in 2015.


* ART was used by '''3.8%''' (2009, 3.6%) of women who gave birth. (see also below [[#Assisted Reproduction Technology|Assisted Reproduction Technology]])
The average age has also increased for Aboriginal and Torres Strait Islander mothers, from 24.9 in 2005 to '''25.6''' in 2015, with a median of 25 years.
* 0.4% (1,267)  of all women who gave planned home birth (2009, 0.3%, 863).


===Smoking during pregnancy===
The proportion of mothers aged 35 and over has increased from 20% in 2005 to 22% (See also [[:File:USA first birth by mother age 1970-2010 graph.gif|USA Data]])


* Smoking while pregnant was reported by 12% of all mothers (2009, 14.5%).
The proportion of mothers aged under 25 has decreased from 19% to 15%.
* More than one‐third (34%) of mothers under 20 smoked in the first 20 weeks of pregnancy
** rate falls to 7% for mothers aged 35–39 but increases slightly to 8% for mothers 40 and over


===Preterm Birth===
The average age of  first‐time mothers also increased, from 28.1 in 2005 to 28.9
{|
| Probably the most significant ongoing issue related to development, with both known and unknown contributors. Importantly, preterm infants also occupy the majority of special care units.


* Australia - '''8.3%''' of babies were born preterm (less than 37 weeks gestation) (2009, 8.2%; 2008, 7.4%).
Multiple pregnancies - represented 1.5% of all pregnancies.
** NSW preterm birth was 7.5% (2010, 7.4%).
* Almost all multiple pregnancies (98%) was {{twinning}} (dizygotic, monozygotic)
* '''0.7%''' post-term (42 weeks gestation or more) (2009, 0.9%).
* Small proportion (2%) were other multiples (triplets, quadruplets or higher).
* [http://www.who.int/maternal_child_adolescent/documents/born_too_soon/en/index.html Born Too Soon: The Global Action Report on Preterm Birth] (2012) The first-ever country-by-country estimate of premature births finds that 15 million babies a year are born preterm - more than one in 10 live births. The report on preterm birth provides the first-ever national, regional and global estimates of preterm birth. The report shows the extent to which preterm birth is on the rise in most countries, and is now the second leading cause of death globally for children under five, after pneumonia. [[Birth_-_Preterm|Preterm Birth]]


:'''Links:''' [http://www.preru.unsw.edu.au/PRERUWeb.nsf/page/ParticipatingUnit Nursery beds]
|-
| [[File:Preterm_birth_screening.jpg|200px]]
! Maternal Conditions
|-
|
* {{smoking}} - One in 10 mothers (31,268 or 10%) who gave birth in 2015 smoked at some time during their pregnancy, a decrease from 11% in 2014 and 15% in 2009.
* {{hypertension}} - 8 per 1,000 mothers had chronic hypertension and 37 per 1,000 had gestational hypertension (preeclampsia)
* {{maternal diabetes}} - 11 per 1,000 had pre‐existing diabetes and 94 per 1,000 had gestational diabetes. (2014 - 10 per 1,000 and 83 per 1,000).
|-
|}
|}
===Multiple pregnancy===
[[Image:Aus_multiple_birth_graph.png|thumb|Australian multiple birth data]]
* The number of multiple births has increased in the last two decades.
* '''4,629''' multiple pregnancies (1.6% of all mothers) (2009, 4,605; 2008, 4,634)
** majority were twin pregnancies (2009, 4,521; 2008, 4,558) fewer triplet pregnancies and other higher-order (2009, 84; 2008, 76)
===Presentation at birth===
[[Image:Galletti1770_breech_01.jpg|thumb|Breech presentation (Galletti, 1770)]]
2009 data
* Cephalic (any part (vertex, face or brow) 94.4% (2008, 94.6%)
* Vertex (crown (vertex) of the fetal head is the presenting part) (2009, 94.2%)
* Breech presentation (buttocks or feet in labour) (2009, 3.9%; 2008, 4.0%)
** 11,565 women with a breech presentation - 92.2% were singleton and 7.8% were multiple pregnancies.
===Method of birth===
2009 data
* vaginal birth 201,631 women
* 56.8% had a non-instrumental vaginal birth.
* instrumental vaginal delivery 11.7%
* caesarean sections 32.3% (2009, 92,687)
* 31.5% nationally (2000 - 23.3%)
{|
{|
| [[Image:Birth caesarean.jpg|300px]]
| [[File:Birth - cephalic presentations.jpg|400px]]


Birth caesarean
Birth - cephalic presentations
| [[File:Australian_caesarean_and_instrumental_birth_2009.jpg|400px]]
| [[File:USA mean age of mother 1970- 2010 graph.png|400px]]


Caesarean and Instrument Delivery
USA mean age of mother (1970-2010)
|}
 
===Pre-existing and pregnancy-related medical conditions===
* The following conditions were also reported: epilepsy, diabetes mellitus and hypertension, antepartum haemorrhage, gestational diabetes, cord prolapse and retained placenta, pregnancy-induced hypertension, fetal distress in labour and post-partum haemorrhage rates
** Note data is not standard across jurisdictions.
 
{{ICD-10}}
 
===Postnatal length of stay===
2009 data
* median postnatal hospital stay for mothers was '''3.0 days'''
* 2.0 days non-instrumental vaginal birth
* 3.0 days vacuum extraction delivery
* 4.0 days caesarean section or forceps delivery
** 5.4% caesarean section had a postnatal length of stay of 7+ days
 
===Maternal death===
2008–2012 data<ref>AIHW: Humphrey MD, Bonello MR, Chughtai A, Macaldowie A, Harris K & Chambers GM 2015. Maternal deaths in Australia 2008–2012. Maternal deaths series no. 5. [http://www.aihw.gov.au/publication-detail/?id=60129551119 Cat. no. PER 70.] Canberra: AIHW.</ref>
* Maternal death in Australia is a rare event in the context of worldwide maternal deaths.
** Aboriginal and Torres Strait Islander women is double that of other Australian women.
* '''105''' maternal deaths in Australia that occurred within 42 days of the end of pregnancy, representing a maternal mortality ratio (MMR) of 7.1 deaths per 100,000 women who gave birth.
* '''49''' maternal deaths directly related to the pregnancy.
** 11 obstetric haemorrhage (5 due to [[Placenta_-_Abnormalities|pathological placentation]], placenta accreta and/or percreta)
** 10 thromboembolism
** 9 hypertensive disorders
|}
|}
==Babies==
==Babies==
{| class="wikitable mw-collapsible mw-collapsed"
{| class="wikitable mw-collapsible mw-collapsed"
! Babies
! Babies &nbsp;
|-
! Gestational Age
|-
|-
|  
|
2009 data
* average gestational age for all babies was 38.6 {{GA}} weeks
* 296,791 live births and 2,341 fetal deaths (2008 - 292,027 live births and 2,177 fetal deaths)
* 91 % born at term (37–41 {{GA}} weeks)
** stillbirth rate of 7.5 per 1,000 births
* most births occurred in October, September and July
* most births occurred in October, September and July
[[Birth_-_Preterm|Pre-term Birth]]
*  '''8.6 %''' born pre‐term (most between 32 and 36 weeks) (8.3 % 2013)
** 7.9 % NSW ([[Australian_Statistics#NSW_Mothers_and_Babies_2015_Report|NSW Report]] [http://www.healthstats.nsw.gov.au/Indicator/mab_pretbth/mab_pretbth NSW Health Statistics])
** higher in - multiple births, indigenous mothers, smokers, remote areas, very young (under 20) and older mothers (40+)
* less than 1% born post‐term (42 weeks and over)


* '''106''' sex ratio, number of male per 100 female liveborn babies. (2008 - 105.6)
[[File:USA births by gestational age 1990-2006 graph.png|400px]]
|-
! [[Birth Weight]]
|-
|
* mean birthweight 3,327 grams
* 92% (282,530) normal birthweight range
* 1.4% (4,263) [[Birth_-_Macrosomia|high birthweight]] (4,500+ grams)
* 6.5% (19,852) low birthweight (less than 2,500 grams)
** 81 % stillborn low birthweight


===Gestational age===
|-
[[File:Special_educational_need_by_gestational_age.jpg|thumb|Special educational need by gestational age (UK data)<ref><pubmed>20543995</pubmed>| [http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1000289 PLoS Medicine]</ref>]]
! [[Apgar_test|Apgar Score]]
2009 data
|-
* '''90.8%''' term, 37–41 weeks gestation. (2008 - 90.9%)
| Apgar score of 7 or more
'''8.2%''' were preterm and '''33.1 weeks''' was the mean gestational age for all preterm births
* 98% all liveborn babies
** Preterm births were classified groups of 20–27 weeks, 28–31 weeks and 32–36 weeks
* 92% pre-term babies
* 92% low birthweight babies (less than 2,500 grams)
* 1 in 5 liveborn babies require active resuscitation


===Birthweight===
|-
[[File:Apgar.jpg|thumb|]]
! Special care nurseries (SCN) or neonatal intensive care units (NICU) Admissions
2009 data
|-
* '''92%''' of liveborn babies had a birthweight in the range 2,500–4,499 grams
|
** average birthweight was 3,374 grams
* 16% (43,348) all Iiveborn babies (2015 - 15%)  
* 18,347 (6.2%) low birthweight (weighing less than 2,500 grams) (2008 - 6.1%)
* 74% Pre-term babies
* 3,017 (1.0%) very low birthweight (weighing less than 1,500 grams)
* majority of multiple births are pre-term
* 1,357 (0.5%) extremely low birthweight (weighing less than 1,000 grams)
* 1.5 times more indigenous babies


Apgar scores - '''1.5%''' of liveborn babies had a low Apgar score (between 0 and 6) at 5 minutes (More? [[Apgar_test|Apgar test]])
[[File:SCN-NCIU-AUS2015 graph.jpg|600px]]
|-
! {{stillbirth}} perinatal mortality
|-
| 2013 and 2014 - 622,037 babies were born in Australia and 6,037 of those babies died in the perinatal period
* 4,419 stillbirths and 1,618 neonatal deaths
* perinatal mortality rate was 9.7 per 1,000 births
* stillbirth (fetal mortality) rate was 7.1 per 1,000 births
* neonatal mortality rate 2.6 per 1,000 live births.
* Between 1995 and 2014 there has been some reduction in neonatal mortality rate, but the stillbirth rate has remained relatively unchanged.
|}


Special care nurseries (SCN) or neonatal intensive care units (NICU) - 14.2% of liveborn babies admitted (2008 - 14.5%)
[[File:Caesarean rates 1990-2014.jpg|600px]]


===Perinatal mortality===
:[[#SDL1|Self-Directed Learning 1]]
[[Image:Perinatal mortality rate NSW 1992-2002.png|thumb|Perinatal mortality rate NSW 1992-2002]]
 
* Different definitions in Australia for reporting and registering perinatal deaths.
** NPDC definition of perinatal deaths to include all fetal and neonatal deaths of at least 400 grams birthweight or at least 20 weeks gestation.
** ABS definition of a perinatal death includes birthweight of at least 400 grams or, where birthweight is unknown, a gestational age of at least 20 weeks.
 
* 2,341 fetal deaths, 7.8 per 1,000 births (2008 - 2,177)
*  667 neonatal deaths (3.0 per 1,000 live births) (2008 - 846)
** neonatal deaths are those occurring in live births up to 28 completed days after birth


*  2,221 Australian perinatal deaths, 70.0% were fetal deaths (2008 - 3,024)
** perinatal death includes birthweight of at least 400 grams or, where birthweight is unknown, a gestational age of at least 20 weeks
* 31.2% congenital abnormalities (anomalies) (2008 - 23.5%)
* 18.9% spontaneous preterm birth


:[[#SDL1|Self-Directed Learning 1]]


|}
{| class="wikitable mw-collapsible mw-collapsed"
{| class="wikitable mw-collapsible mw-collapsed"
! 2013 National core maternity indicators
! 2013 National core maternity indicators &nbsp;
|-
|-
| [[File:National_core_maternity_indicators_2013.jpg|150px|right]]
| [[File:National_core_maternity_indicators_2013.jpg|150px|right]]
Line 261: Line 217:


This report provides a baseline for monitoring changes in the quality of maternity services across Australia using 10 national core maternity indicators.
This report provides a baseline for monitoring changes in the quality of maternity services across Australia using 10 national core maternity indicators.
# Smoking in pregnancy for all women giving birth
# [[Abnormal Development - Smoking|Smoking]] in pregnancy for all women giving birth
# Antenatal care in the first trimester for all women giving birth
# Antenatal care in the first trimester for all women giving birth
# Episiotomy for women having their first baby and giving birth vaginally
# Episiotomy for women having their first baby and giving birth vaginally
# Apgar score of less than 7 at 5 minutes for births at or after term
# [[Apgar_test|Apgar Score]] of less than 7 at 5 minutes for births at or after term
# Induction of labour for selected women giving birth for the first time
# Induction of labour for selected women giving birth for the first time
# Caesarean section for selected women giving birth for the first time
# Caesarean section for selected women giving birth for the first time
Line 278: Line 234:


== Unintended Pregnancy ==
== Unintended Pregnancy ==
{|
A recent 2018 USA study{{#pmid:29501647|PMID29501647}} of Unintended pregnancy and interpregnancy interval by maternal age, [https://www.cdc.gov/nchs/nsfg/index.htm National Survey of Family Growth].
| Approximately one-half of pregnancies in the United States (2001) were unintended (Finer 2006, Perspectives on Sexual and Reproductive Health).
 
An earlier 1995 USA National Survey of Family Growth (NSFG) found:
 
* '''40%''' of pregnancies were unintended  
* '''36%''' followed an interpregnancy interval (IPI) less than 18 months.  
* Within each maternal age group, the percentage of pregnancies that were unintended decreased as IPI increased.


* 49% of pregnancies in the USA (excluding miscarriages)
* 31% of pregnancies resulting in a live birth are unintended


Unintended pregnancy is either mistimed (woman wanted to be pregnant later) or unwanted (did not want to ever be pregnant).
Unintended pregnancy is either mistimed (woman wanted to be pregnant later) or unwanted (did not want to ever be pregnant).


| [[Image:Teen pregnancy USA.png|300px]]


Teen pregnancy (USA)
'''Australian Teenage Pregnancy Statistics''' (2015) [https://www.aihw.gov.au/reports/mothers-babies/teenage-mothers-in-australia-2015/contents/table-of-contents AIHW]
|}
 
[[File:Australian teenage mothers and birth rate 2015.jpg|600px]]
<br>
* Rate of teenage births in Australia is in decline, from '''17.5''' births per 1,000 women in 2005 to '''11.4''' in 2015
* Babies of teenage mothers were 1.3 times as likely to be of low birthweight than babies of 20-24 year old mothers
* Babies of teenage mothers were 1.2 times as likely to be preterm than babies of 20-24 year old mothers
* 1 in 4 teenage mothers smoked after 20 weeks of pregnancy
 
<br>
{| class="wikitable mw-collapsible mw-collapsed"
{| class="wikitable mw-collapsible mw-collapsed"
! Teen Pregnancy
! Unintended and Teen Pregnancy &nbsp;
|-
| 2001 USA - Approximately one-half of pregnancies in the United States were unintended (Finer 2006, Perspectives on Sexual and Reproductive Health).
An earlier 1995 USA National Survey of Family Growth (NSFG) found:
 
* 49% of pregnancies in the USA (excluding miscarriages)
* 31% of pregnancies resulting in a live birth are unintended
| [[File:Teen pregnancy USA.png|400px]]
|-
|-
| A recent Canadian retrospective study<ref><pubmed>23470111</pubmed></ref> of half a million births comparing pregnant women < 20 years of age (adolescent) were compared with those of women 20 to 35 years old.  
| colspan=2|A recent Canadian retrospective study{{#pmid:23470111|PMID23470111}} of half a million births comparing pregnant women < 20 years of age (adolescent) were compared with those of women 20 to 35 years old.  
* Adolescents had a higher rate of smoking and substance use than adult women and were within the lowest education and family income quintiles.
* Adolescents had a higher rate of smoking and substance use than adult women and were within the lowest education and family income quintiles.
* Adolescents had a significantly lower risk of gestational hypertension, gestational diabetes, placental abruption, and placenta previa, but their risk of preterm premature rupture of membranes was significantly higher.   
* Adolescents had a significantly lower risk of gestational hypertension, gestational diabetes, placental abruption, and placenta previa, but their risk of preterm premature rupture of membranes was significantly higher.   
Line 305: Line 276:
'''Links:''' [http://www.cdc.gov/reproductivehealth/UnintendedPregnancy/index.htm CDC Unintended Pregnancy Prevention] |  [http://www.cdc.gov/prams/ Pregnancy Risk Assessment Monitoring System USA] | [http://www.guttmacher.org/pubs/journals/3509403.html The Measurement and Meaning of Unintended Pregnancy]
'''Links:''' [http://www.cdc.gov/reproductivehealth/UnintendedPregnancy/index.htm CDC Unintended Pregnancy Prevention] |  [http://www.cdc.gov/prams/ Pregnancy Risk Assessment Monitoring System USA] | [http://www.guttmacher.org/pubs/journals/3509403.html The Measurement and Meaning of Unintended Pregnancy]
== Assisted Reproduction Technology  ==
== Assisted Reproduction Technology  ==
[[File:Assisted reproductive technology in Australia and New Zealand 2013.jpg|thumb|Assisted reproductive technology in Australia and New Zealand 2013]]
[[File:Assisted reproductive technology in Australia and New Zealand 2015.jpg|thumb|Assisted reproductive technology in Australia and New Zealand 2015]]
Assisted Reproduction Technology (ART) is also sometimes also used to identify In vitro fertilization (IVF) but now includes many new techniques.  
Assisted Reproduction Technology (ART) is also sometimes also used to identify In vitro fertilization (IVF) but now includes many new techniques. Assisted reproductive technology (ART) is a group of procedures that involve the in vitro (outside of body) handling of human oocytes (eggs) and sperm or embryos for the purposes of establishing a pregnancy. Each ART treatment involves a number of stages and is generally referred to as an ART treatment cycle. The embryos transferred to a women can either originate from the cycle in which they were created (fresh cycle) or be frozen and thawed before transfer (thaw cycle).
 
Assisted Reproductive Technology in Australia and New Zealand (2015)<ref>{{Ref-ART2015}}</ref>
 
* 77,721 ART treatment cycles reported from Australian and New Zealand clinics in 2015 (71,479 and 6,242 respectively)
** 5.6% increase in Australia and 6.0% increase in New Zealand on 2014.
** 14.4 cycles per 1,000 women of reproductive age (15–44 years) in Australia
** 94.5% autologous cycles (own oocytes or embryos)
** 37.4% autologous frozen and thawed
** 39,006 women who undertook 73,481 autologous fresh and/or thaw cycles
** Over the last five years there has been an increasing trend in the proportion of cycles where all oocytes or embryos are cryopreserved for potential future use from (2011) 5.0% (2015) 17.2%
 
* 35.8 years - average age of women undergoing autologous cycles
** 40.6 years - average age of women undergoing ART treatment using donor oocytes or embryos
** 24.8% were aged 40 or older. The average age of the male partner of the women undergoing autologous and recipient cycles was ** 38.1 years - average age of the male partner
 
* 22.8% (17,726) resulted in a clinical pregnancy
* 18.1% (14,040) in a live delivery
** higher live delivery rate in younger women.
*** under 30 - live delivery rate per embryo transfer 38.4% for autologous fresh cycles and 32.6% for autologous thaw cycles
*** women aged over 44 -  live delivery rate was 0.7% per embryo transfer for autologous fresh and 7.6% thaw cycles.
 
* 14,791 babies born (including 14,655 liveborn babies)
** 78.8% were full-term singletons of normal birthweight.
 
* shift from cleavage stage transfers to blastocyst transfers (from 57.7% in 2011 to 73.5% in 2015)
* increase in vitrification as a cryopreservation method (from 73.0% of thaw blastocyst transfer cycles in 2011 to 86.1% in 2015).
* intracytoplasmic sperm injection (ICSI) has remained stable at around 63% of embryo transfer cycles in 2011-2015.
 
* 36% decrease in Multiple births from 6.9% in 2011 to 4.4% in 2015.
 
 
 


Assisted Reproductive Technology in Australia and New Zealand (2013)<ref>Macaldowie A, Lee E & Chambers GM 2015. Assisted reproductive technology in Australia and New Zealand 2013. Sydney: National Perinatal Epidemiology and Statistics Unit, the University of New South Wales. [https://npesu.unsw.edu.au/surveillance/assisted-reproductive-technology-australia-new-zealand-2013 NPESU]</ref>
{| class="wikitable mw-collapsible mw-collapsed"
! Australia 2013 Data
|-  
|
* 71,516 ART treatment cycles reported from Australian and New Zealand clinics in 2013 (66,143 and 5,373 respectively).
* 71,516 ART treatment cycles reported from Australian and New Zealand clinics in 2013 (66,143 and 5,373 respectively).
** 1.9% increase in Australia and 3.8% increase in New Zealand on 2012.  
** 1.9% increase in Australia and 3.8% increase in New Zealand on 2012.  
Line 319: Line 325:
** more cycles per woman in Australia (1.9 cycles per woman) than in New Zealand (1.5 cycles per woman).  
** more cycles per woman in Australia (1.9 cycles per woman) than in New Zealand (1.5 cycles per woman).  
* [[Preimplantation Genetic Diagnosis]] (PGD) was performed in 2,740 cycles (19.4% increase), 4.4% of cycles in which embryos were created or thawed.
* [[Preimplantation Genetic Diagnosis]] (PGD) was performed in 2,740 cycles (19.4% increase), 4.4% of cycles in which embryos were created or thawed.
 
|-
 
{| class="wikitable mw-collapsible mw-collapsed"
! Australia 2012 Data
! Australia 2012 Data
|-  
|-  
Line 373: Line 377:
===Hydatidiform Mole===
===Hydatidiform Mole===
[[File:Hydatidiform mole.jpg|thumb|Hydatidiform Mole]]
[[File:Hydatidiform mole.jpg|thumb|Hydatidiform Mole]]
Another type of abnormality is when only the conceptus trophoblast layers proliferates and not the embryoblast, no embryo develops, this is called a "hydatidiform mole", which is due to the continuing presence of the trophoblastic layer, this abnormal conceptus can also implant in the uterus. The trophoblast cells will secrete human chorionic gonadotropin (hCG), as in a normal pregnancy, and may appear maternally and by pregnancy test to be "normal". Prenatal diagnosis by ultrasound analysis demonstrates the absence of a embryo.  
Another type of abnormality is when only the conceptus trophoblast layers proliferates and not the embryoblast, no embryo develops, this is called a [[Abnormal_Development_-_Hydatidiform_Mole|"hydatidiform mole"]], which is due to the continuing presence of the trophoblastic layer, this abnormal conceptus can also implant in the uterus. The trophoblast cells will secrete human chorionic gonadotropin (hCG), as in a normal pregnancy, and may appear maternally and by pregnancy test to be "normal". Prenatal diagnosis by ultrasound analysis demonstrates the absence of a embryo.  


There are several forms of hydatidiform mole: partial mole, complete mole and persistent gestational trophoblastic tumor. Many of these tumours arise from a haploid sperm fertilizing an egg without a female pronucleus (the alternative form, an embryo without sperm contribution, is called parthenogenesis). The tumour has a "grape-like" placental appearance without enclosed embryo formation. Following a first molar pregnancy, there is approximately a 1% risk of a second molar pregnancy.
There are several forms of hydatidiform mole: partial mole, complete mole and persistent gestational trophoblastic tumor. Many of these tumours arise from a haploid sperm fertilizing an egg without a female pronucleus (the alternative form, an embryo without sperm contribution, is called parthenogenesis). The tumour has a "grape-like" placental appearance without enclosed embryo formation. Following a first molar pregnancy, there is approximately a 1% risk of a second molar pregnancy.
Line 380: Line 384:


===Twinning===
===Twinning===
* '''Twin deliveries and place of birth in NSW 2001-2005'''<ref><pubmed>19780726</pubmed></ref> "Both infant and maternal morbidity increase from 39 weeks gestation. Delivery of twins before 36 weeks at smaller hospitals (< 500 deliveries per annum) should be avoided. A twin pregnancy where there is a greater or equal to 20% difference in estimated fetal weights should be considered for referral to a tertiary obstetric unit."
* '''Twin deliveries and place of birth in NSW 2001-2005'''{{#pmid:19780726|PMID19780726}} "Both infant and maternal morbidity increase from 39 weeks gestation. Delivery of twins before 36 weeks at smaller hospitals (< 500 deliveries per annum) should be avoided. A twin pregnancy where there is a greater or equal to 20% difference in estimated fetal weights should be considered for referral to a tertiary obstetric unit."


====Dizygotic  Twinning====
====Dizygotic  Twinning====
Line 389: Line 393:
Monoygotic twins (identical) produced from a single [[F#fertilization|fertilization]] event (one fertilised egg and a single spermatazoa, form a single zygote), these twins therefore share the same genetic makeup. Occurs in approximately 3-5 per 1000 pregnancies, more commonly with aged mothers. The later the twinning event, the less common are initially separate placental membranes and finally resulting in conjoined twins.
Monoygotic twins (identical) produced from a single [[F#fertilization|fertilization]] event (one fertilised egg and a single spermatazoa, form a single zygote), these twins therefore share the same genetic makeup. Occurs in approximately 3-5 per 1000 pregnancies, more commonly with aged mothers. The later the twinning event, the less common are initially separate placental membranes and finally resulting in conjoined twins.


{| class="prettytable" 100%
{{Monoygotic Twinning Table}}
| width=10% | '''Week'''
|
| colspan="7" | Week 1
| colspan="7" | Week 2
 
|-bgcolor="lightsteelblue"
| '''Day'''
| width=5% | 0
| width=5% | 1
| width=5% | 2
| width=5% | 3
| width=5% | 4
| width=5% | 5
| width=5% | 6
| width=5% | 7
| width=5% | 8
| width=5% | 9
| width=5% | 10
| width=5% | 11
| width=5% | 12
| width=5% | 13
| width=5% | 14
 
|-
| '''Cell Number'''
| 1
| 1
| 2
| 16
| 32
| 128
|
|
|
| bilaminar
|
|
|
|
|
 
|-
| '''Event'''
| Ovulation
| fertilization
| First cell division
| Morula
| Early blastocyst
| Late blastocyst
 
Hatching
| Implantation starts
|
|
| X inactivation
|
|
|
|
|
 
|-
|
| [[File:Follicle 001 icon.jpg|50px]]
| [[File:Early_zygote.jpg|50px]]
| [[File:Human embryo day 2.jpg|50px]]
| [[File:Human embryo day 3.jpg|50px]]
| [[File:Human embryo day 5.jpg|50px]]
| [[File:CSt3.jpg|50px]]
| [[File:Week2_001 icon.jpg|50px]]
|
|
|
|
|
|
|
|
|-bgcolor="lightsteelblue"
| '''Monoygotic'''
 
'''Twin Type'''
|
| colspan="3" | Diamniotic
 
Dichorionic
| colspan="3" | Diamniotic
 
Monochorionic
| colspan="3" | Monoamniotic
 
Monochorionic
| colspan="5" | Conjoined
 
|-
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
 
|}
 
Table based upon recent Twinning Review.<ref><pubmed>12957099</pubmed></ref>


:'''Links:''' [[Abnormal_Development_-_Twinning|Twinning]]
:'''Links:''' [[Abnormal_Development_-_Twinning|Twinning]]
Line 534: Line 423:
! NIPT - Non-Invasive Prenatal Testing
! NIPT - Non-Invasive Prenatal Testing
|-
|-
| '''Fetal aneuploidy screening with cell-free DNA in late gestation'''<ref name=PMID27124739><pubmed>27124739</pubmed></ref>"The aim of this study was to evaluate clinical use of NIPT at gestational ages of 23 weeks and above. A cohort of 5579 clinical patients with singleton gestations of 23 weeks or greater submitting a blood sample for NIPT in an 18-month period were selected for this study. ...Of 5372 reported late-gestation samples, 151 (2.8%) were reported as aneuploidy detected or suspected. In late-gestation samples, the overall observed positive predictive value (PPV) for NIPT was 64.7%, with an observed PPV of 100% in the subset of cases with multiple clinical indications including abnormal ultrasound findings. NIPT is a highly accurate prenatal screening option for women after 23 weeks of gestation. Women who presented for NIPT in the latter stages of pregnancy more frequently specified clinical indications of abnormal ultrasound findings than women who entered screening earlier in pregnancy."
| '''Fetal aneuploidy screening with cell-free DNA in late gestation'''{{#pmid:27124739|PMID27124739}}"The aim of this study was to evaluate clinical use of NIPT at gestational ages of 23 weeks and above. A cohort of 5579 clinical patients with singleton gestations of 23 weeks or greater submitting a blood sample for NIPT in an 18-month period were selected for this study. ...Of 5372 reported late-gestation samples, 151 (2.8%) were reported as aneuploidy detected or suspected. In late-gestation samples, the overall observed positive predictive value (PPV) for NIPT was 64.7%, with an observed PPV of 100% in the subset of cases with multiple clinical indications including abnormal ultrasound findings. NIPT is a highly accurate prenatal screening option for women after 23 weeks of gestation. Women who presented for NIPT in the latter stages of pregnancy more frequently specified clinical indications of abnormal ultrasound findings than women who entered screening earlier in pregnancy."


More? [[Fetal Cells in Maternal Blood]] | [http://www.racgp.org.au/afp/2014/july/noninvasive-prenatal-testing/ RACGP] | [http://www.nchpeg.org/index.php?option=com_content&view=article&id=384 NCHPEG]
More? [[Fetal Cells in Maternal Blood]] | [http://www.racgp.org.au/afp/2014/july/noninvasive-prenatal-testing/ RACGP] | [http://www.nchpeg.org/index.php?option=com_content&view=article&id=384 NCHPEG]
Line 592: Line 481:
'''Links:''' [http://www0.health.nsw.gov.au/policies/pd/2012/PD2012_055.html NSW Health - Congenital Conditions Register - Reporting Requirements 2012] | [http://www0.health.nsw.gov.au/policies/pd/2012/pdf/PD2012_055.pdf PDF]
'''Links:''' [http://www0.health.nsw.gov.au/policies/pd/2012/PD2012_055.html NSW Health - Congenital Conditions Register - Reporting Requirements 2012] | [http://www0.health.nsw.gov.au/policies/pd/2012/pdf/PD2012_055.pdf PDF]


===Mothers and Babies Report 2010===
* preterm birth (less than 37 weeks gestation) was 7.4%.
* rate of low birth weight (less than 2,500 grams) was 6.1%
** in Aboriginal or Torres Strait Islander babies was 11.2%.
* About 2% of infants are born with congenital conditions each year in NSW.
* In 2004–2010, anomalies of the '''cardiovascular''' system were most commonly reported, followed by anomalies of the '''musculoskeletal''' system and the '''genito-urinary''' system.
* Congenital conditions were more common among premature infants compared to full term infants, and among male infants compared to female infants.
* rate of congenital conditions increases with increasing maternal age, especially after age 35.
** However, as most babies are born to mothers aged less than 35 years, the majority of babies with congenital conditions were born to younger mothers.
* perinatal deaths 755, 134 (17.7%) of these deaths were unexplained stillbirths.
* neonatal death was extreme prematurity (41.3%), followed by congenital abnormalities (21.5%).


Data<refCentre for Epidemiology and Evidence. New South Wales Mothers and Babies 2010. Sydney: NSW Ministry of Health, 2012.</ref>
===NSW Mothers and Babies Report 2015===
[[File:New South Wales Mothers and Babies 2015.jpg|thumb|alt=New South Wales Mothers and Babies 2015 cover|New South Wales Mothers and Babies 2015]]
[[File:NSW Perinatal Data Collection form.png|thumb|alt=NSW Perinatal Data Collection form|NSW Perinatal Data Collection form]]
NSW is one of the largest states in Australia by population. The New South Wales Perinatal Data Collection (PDC) is a population-based surveillance system covering all births in NSW public and private hospitals, as well as home births. It encompasses all live births, and stillbirths of at least 20 weeks gestation or at least 400 grams birth weight.<ref name=NSWMB15>Centre for Epidemiology and Evidence. [http://www.health.nsw.gov.au/hsnsw/Publications/mothers-and-babies-2015.pdf New South Wales Mothers and Babies 2015]. Sydney: [http://www.health.nsw.gov.au/hsnsw/Pages/mothers-and-babies-2015.aspx NSW Ministry of Health], 2016.</ref>
 
* Number of births decreased from 97,245 in 2011 to 96,391 in 2015 (decrease of 0.9%).
* Percentage of teenage mothers fell from 3.2% in 2011 to 2.5% in 2015.
* Rate of normal vaginal birth decreased from 56.9% in 2011 to 56.0% in 2015.
* Operative and instrumental births were more common among privately than publicly insured mothers.
* Proportion of smoking mothers during pregnancy declined from 11.1% in 2011 to 8.9% in 2015.
* Majority of mothers planned to give birth in a hospital labour ward
** 87% per cent of mothers who planned to give birth in a birth centre actually did so.
** There were 187 homebirths in NSW reported in 2015.
* Premature babies (less than 37 weeks gestation) 7.9% (slight increase from 7.5% in 2011).
* Since 2011, the rate of low birth weight (less than 2,500 grams) has remained stable, ranging from 6.1% to 6.6%.
** Low birth weight rate was 6.6% in 2015.
* Between 2011 and 2015, the reported number of Aboriginal or Torres Strait Islander mothers giving birth increased from 2,975 to 3,823, an increase from 3.1% to 4.0% of all mothers.
* Aboriginal or Torres Strait Islander
** teenage mothers fell from 19.0% in 2011 to 15.4% in 2015.
** 45.0% of Aboriginal or Torres Strait Islander mothers reported smoking during pregnancy.
** Since 2011, rates of low birth weight and prematurity in Aboriginal or Torres Strait Islander babies has been over 11%. In 2015, 11.3% of Aboriginal or Torres Strait Islander babies were low birth weight and 12.7% were premature.
** Perinatal mortality rate of 9.6 per 1,000 births in Aboriginal or Torres Strait Islander mothers in 2015 is higher than the rate of 8.1 per 1,000 births experienced among babies born to non-Aboriginal or Torres Strait Islander mothers.


'''Links:''' [http://www.health.nsw.gov.au/publications/Pages/mothers-and-babies-2010.aspx New South Wales Mothers and Babies Report 2010]


{{Victoria abnormal data table 2004}}
{{Victoria abnormal data table 2004}}
Line 699: Line 597:


* '''Teratogen synergism''', different environmental effects can act individually or in combination on the same developing system. For example, neural development can be impacted upon by alcohol (fetal alcohol syndrome), viral infection (rubella) and/or inadequate dietry folate intake (neural tube defects). These effects may also not be seen as a direct effect on a system or systems but result in a reduced birth weight and the potential postnatal developmental effects. Consider also this in relation to the increasing support to the '''fetal origins hypothesis'''.
* '''Teratogen synergism''', different environmental effects can act individually or in combination on the same developing system. For example, neural development can be impacted upon by alcohol (fetal alcohol syndrome), viral infection (rubella) and/or inadequate dietry folate intake (neural tube defects). These effects may also not be seen as a direct effect on a system or systems but result in a reduced birth weight and the potential postnatal developmental effects. Consider also this in relation to the increasing support to the '''fetal origins hypothesis'''.
* Alcohol - In utero alcohol effects on foetal, neonatal and childhood lung disease.{{#pmid:27613232|PMID27613232}}


'''Links:'''  
'''Links:'''  
Line 709: Line 610:
* Finally, when studying this topic remember the concept of critical periods of development that will affect the overall impact of the above listed factors. This can be extended to the potential differences between prenatal and postnatal effects, for example with infections and outcomes.
* Finally, when studying this topic remember the concept of critical periods of development that will affect the overall impact of the above listed factors. This can be extended to the potential differences between prenatal and postnatal effects, for example with infections and outcomes.


{| class="prettytable"
| bgcolor= "LightCyan" colspan="2" | '''Conceptus'''
| bgcolor= "LightBlue" colspan="13" | '''Embryonic development''' (weeks)
| bgcolor= "LightSkyBlue" colspan="5" | '''Fetal period''' (weeks)


|-
{{Critical Periods table}}
| bgcolor= "LightCyan" width="50px" |<center>'''1'''</center>
| bgcolor= "LightCyan" width="50px" |<center>'''2'''</center>
| bgcolor= "LightBlue" width="50px" colspan="2" |<center>'''3'''</center>
| bgcolor= "LightBlue" width="50px" colspan="3" |<center>'''4'''</center>
| bgcolor= "LightBlue" width="50px" | <center>'''5'''</center>
| bgcolor= "LightBlue" width="50px" colspan="2" | <center>'''6'''</center>
| bgcolor= "LightBlue" width="50px" colspan="2" | <center>'''7'''</center>
| bgcolor= "LightBlue" width="50px" colspan="3" | <center>'''8'''</center>
| bgcolor= "LightSkyBlue" width="50px" colspan="2" | <center>'''9'''</center>
| bgcolor= "LightSkyBlue" width="50px" | <center>'''16'''</center>
| bgcolor= "LightSkyBlue" width="50px" | <center>'''20-36'''</center>
| bgcolor= "LightSkyBlue" width="50px" | <center>'''38'''</center>


|-
| bgcolor= "LightCyan" width="50px" | [[File:Early_zygote.jpg|50px]]
| bgcolor= "LightCyan" width="50px" | [[File:Week2_001 icon.jpg|50px]]
| bgcolor= "LightBlue" width="50px" colspan="2" |[[File:Stage9_sem4c.jpg|50px]]
| bgcolor= "LightBlue" width="50px" colspan="3" |[[File:Stage13_sem1c.jpg|50px]]
| bgcolor= "LightBlue" width="50px" |[[File:Stage15_bf1c.jpg|50px]]
| bgcolor= "LightBlue" width="50px" colspan="2" |[[File:Stage17_bf1c.jpg|50px]]
| bgcolor= "LightBlue" width="50px" colspan="2" |[[File:Stage19_bf1c.jpg|50px]]
| bgcolor= "LightBlue" width="50px" colspan="3" |[[File:Stage23_bf1c.jpg|50px]]
| bgcolor= "LightSkyBlue" width="50px" colspan="2" |
| bgcolor= "LightSkyBlue" width="50px" |
| bgcolor= "LightSkyBlue" width="50px" |
| bgcolor= "LightSkyBlue" width="50px" |


|-
:[[#SDL6|Self-Directed Learning 6]]
|
|
| bgcolor= "Salmon" colspan="16" | '''Neural'''
| bgcolor= "LightSalmon" colspan="2" |


|-
'''Links:''' [[Embryonic Development]] | [[Timeline_human_development|Timeline human development]] | [[Movie - Human Development annotated cartoon]] | [[:File:Human-critical_periods.jpg|Human - critical periods]]
| [[File:Stage2.jpg|50px]]
|
|
| bgcolor= "Salmon" colspan="6" | '''Heart'''
| bgcolor= "LightSalmon" colspan="6" |
|
|
|
|
|
 
|-
|
|
|
|
| bgcolor= "Salmon" colspan="6" | '''Upper limbs'''
| bgcolor= "LightSalmon" colspan="5" |
|
|
|
|
|


|-
|
|
|
|
|
| bgcolor= "Salmon" colspan="6" | '''Lower limbs'''
| bgcolor= "LightSalmon" colspan="4" |
|
|
|
|
|


|-
==Australian Drug Categories==
|
Legal drugs are classified, usually by each country's appropriate regulatory body, on the safety of drugs during pregnancy. In Australia, the Therapeutic Goods Authority has classes (A, B1, B2, B3, C, D and X) to define their safety. (More? [[Australian Drug Categories]]) In the USA, since 2015 drugs are classified by the Food and Drug Administration (FDA) into new classes to define their safety.  The Australian categorisation of medicines for use in pregnancy does not follow a hierarchical structure.
|
|
|
|
| bgcolor= "Salmon" colspan="9" | '''Ear'''
| bgcolor= "LightSalmon" colspan="4" |
|
|
 
|-
|
|
|
|
|
|
| bgcolor= "Salmon" colspan="7" | '''Eye'''
| bgcolor= "LightSalmon" colspan="7" |
 
|-
| [[File:CSt3.jpg|50px]]
|
|
|
|
|
|
|
|
| bgcolor= "Salmon" colspan="7" | '''Palate'''
| bgcolor= "LightSalmon" |
|
|
|
 
|-
|
|
|
|
|
|
|
|
|
| bgcolor= "Salmon" colspan="6" | '''Teeth'''
| bgcolor= "LightSalmon" colspan="5" |
 
|-
| [[File:Week2_001 icon.jpg|50px]]
|
|
|
|
|
|
|
|
|
|
| bgcolor= "Salmon" colspan="5" | '''External genitalia'''
| bgcolor= "LightSalmon" colspan="4" |
 
|-
| bgcolor= "LightCyan" colspan="2" | '''Loss'''
| bgcolor= "Salmon" colspan="10" | '''Major abnormalities'''
| bgcolor= "LightSalmon" colspan="8" | '''Functional and Minor abnormalities'''
 
|}
 
:[[#SDL6|Self-Directed Learning 6]]


'''Links:''' [[Embryonic Development]] | [[Timeline_human_development|Timeline human development]] | [[Movie - Human Development annotated cartoon]] | [[:File:Human-critical_periods.jpg|Human - critical periods]]
* Human data are lacking or inadequate for drugs in the B1, B2 and B3 categories
* Subcategorisation of the B category is based on animal data
* The allocation of a B category does not imply greater safety than a C category
* Medicines in category D are not absolutely contraindicated during pregnancy (e.g.anticonvulsants)


==Australian Drug Categories==
Legal drugs are classified, usually by each country's appropriate regulatory body, on the safety of drugs during pregnancy. In Australia, the Therapeutic Goods Authority has classes (A, B1, B2, B3, C, D and X) to define their safety. In the USA, drugs are classified by the Food and Drug Administration (FDA) into classes (A, B, C, D, and X) to define their safety. (More? [[Australian Drug Categories]])


* '''Pregnancy Category A''' - Have been taken by a large number of pregnant women and women of childbearing age without an increase in the frequency of malformations or other direct or indirect harmful effects on the fetus having been observed.  
* '''Pregnancy Category A''' - Have been taken by a large number of pregnant women and women of childbearing age without an increase in the frequency of malformations or other direct or indirect harmful effects on the fetus having been observed.  
Line 879: Line 641:


* '''Pregnancy Category X''' - Have such a high risk of causing permanent damage to the fetus that they should NOT be used in pregnancy or when there is a possibility of pregnancy.  
* '''Pregnancy Category X''' - Have such a high risk of causing permanent damage to the fetus that they should NOT be used in pregnancy or when there is a possibility of pregnancy.  
<br>
{| class="wikitable mw-collapsible mw-collapsed"
! US FDA - 2015 Pregnancy and Lactation Labeling (Drugs) 2015 &nbsp;
|-
| [[File:FDA drug category changes 2015.jpg|800px]]
|-
| Since 2015 the labelling classes (A, B, C, D, and X) have been replaced with the new "FDA Pregnancy and Lactation Labeling Rule" (PLLR).
|-
| Links: [[USA Drug Categories]] | [https://www.fda.gov/Drugs/DevelopmentApprovalProcess/DevelopmentResources/Labeling/ucm093307.htm Pregnancy and Lactation Labeling (Drugs) Final Rule]
|}


===Infant Drug Clearance===
===Infant Drug Clearance===
[[Image:Drug-clearance-rates.png|thumb|Drug clearance rates]]
[[File:Drug-clearance-rates.png|thumb|Drug clearance rates]]
The drug clearance data below are only approximate calculated rates for the fetus and infant from [http://www.medsafe.govt.nz/Profs/PUarticles/lactation.htm#Infants NZ Drug Safety in Lactation]
The drug clearance data below are only approximate calculated rates for the fetus and infant from [http://www.medsafe.govt.nz/Profs/PUarticles/lactation.htm#Infants NZ Drug Safety in Lactation]
{| class="prettytable"
{| class="prettytable"
Line 1,046: Line 819:
* '''Other''' Motherisk (Canada) [http://www.motherisk.org/women/drugs.jsp Drugs, chemicals, radiation and herbal products in pregnancy] | International Society for the Study of Trophoblastic Diseases [http://www.isstd.org/intro/index.html Trophoblastic Diseases]
* '''Other''' Motherisk (Canada) [http://www.motherisk.org/women/drugs.jsp Drugs, chemicals, radiation and herbal products in pregnancy] | International Society for the Study of Trophoblastic Diseases [http://www.isstd.org/intro/index.html Trophoblastic Diseases]


* '''Europe''' {{Ref-ESHRE_Atlas2012}}


{{Glossary}}
{{Glossary}}

Revision as of 11:50, 21 May 2019

Embryology - 28 Mar 2024    Facebook link Pinterest link Twitter link  Expand to Translate  
Google Translate - select your language from the list shown below (this will open a new external page)

العربية | català | 中文 | 中國傳統的 | français | Deutsche | עִברִית | हिंदी | bahasa Indonesia | italiano | 日本語 | 한국어 | မြန်မာ | Pilipino | Polskie | português | ਪੰਜਾਬੀ ਦੇ | Română | русский | Español | Swahili | Svensk | ไทย | Türkçe | اردو | ייִדיש | Tiếng Việt    These external translations are automated and may not be accurate. (More? About Translations)

Introduction

Chris.jpg

This Medicine Phase 2 tutorial introduces the topics of Applied Embryology and Teratology. This one and a half hour presentation uses your existing knowledge of normal human development in an applied clinical manner in relation to our existing knowledge of teratogens. In addition, you should begin considering the variables that will not change and those that will in future medical practice. Due to time limitations, only a brief coverage can be given of any one topic.


Self-Directed Learning boxes on this page will not be discussed within the tutorial. You should also return here and later work through the linked online resources for more detailed descriptions and an understanding of these issues. This current page appears in the lefthand menu under Medicine as BGD 2 Tutorial.


      Tinycc page - http://tiny.cc/BGD2_Tutorial


Similar content was covered in the previous online tutorials in

2018 | 2018 PDF | 2017 | 2016 | 2015 | 2014 | 2012 | 2015 PDF | 2014 PDF | 2012 PDF | 2011 PDF and 2010.

Whats in the News?  
Australian maternal physical activity 2011-2012
Australian maternal physical activity 2011-2012
  • This report looks at the types and amount of physical activity undertaken by women during pregnancy using the Australian Bureau of Statistics’ Australian Health Survey 2011–12. It compares activity levels for pregnant and non-pregnant women of the same ages and assesses these levels against the Australian physical activity guideline for adults.[1]
    • Only 3 in 10 pregnant women met the physical activity guideline
    • Two-thirds of pregnant women were active for fewer than 150 minutes per week
    • Just over half of pregnant women exercised for fitness, usually walking
Endocrine disrupting chemicals historical timeline
Endocrine disrupting chemicals historical timeline[2]
  • Endocrine Disrupting Chemicals: An Occult Mediator of Metabolic Disease[2] "Endocrine disrupting chemicals (EDCs), a heterogeneous group of exogenous chemicals that can interfere with any aspect of endogenous hormones, represent an emerging global threat for human metabolism. There is now considerable evidence that the observed upsurge of metabolic disease cannot be fully attributed to increased caloric intake, physical inactivity, sleep deficit, and ageing. Among environmental factors implicated in the global deterioration of metabolic health, EDCs have drawn the biggest attention of scientific community, and not unjustifiably. EDCs unleash a coordinated attack toward multiple components of human metabolism, including crucial, metabolically-active organs such as hypothalamus, adipose tissue, pancreatic beta cells, skeletal muscle, and liver. Specifically, EDCs' impact during critical developmental windows can promote the disruption of individual or multiple systems involved in metabolism, via inducing epigenetic changes that can permanently alter the epigenome in the germline, enabling changes to be transmitted to the subsequent generations. The clear effect of this multifaceted attack is the manifestation of metabolic disease, clinically expressed as obesity, metabolic syndrome, diabetes mellitus, and non-alcoholic fatty liver disease."
  • Maternal Vaccination - The Safety of Influenza and Pertussis Vaccination in Pregnancy in a Cohort of Australian Mother-Infant Pairs, 2012-2015: The FluMum Study[3] "Inactivated influenza vaccine (IIV) and pertussis vaccination are recommended in pregnancy. Limited safety data exist for women who received IIV vaccine during the first trimester of pregnancy or received both vaccines in pregnancy. We assessed adverse birth outcomes between vaccinated and unvaccinated pregnancies. METHODS: Among prospectively enrolled Australian "FluMum" participants (2012-2015), primary exposure was receipt and timing of IIV during pregnancy. Primary outcomes included preterm birth, low birthweight at term (LBWT), and small for gestational age (SGA). We compared birth outcomes for IIV in pregnancy with women unvaccinated in pregnancy using Cox proportional hazard ratios (HRs) with 95% confidence intervals (CIs). ...No significant associations were found between maternal IIV or pertussis vaccination in pregnancy and adverse birth outcomes, regardless of the trimester of pregnancy a vaccination was given compared to unvaccinated pregnancies."
    • (No) Association between seasonal influenza vaccination with pre- and postnatal outcomes[4] "This study found no evidence of adverse maternal and infant outcomes associated with seasonal influenza vaccine during pregnancy. On the contrary, vaccinated women were less likely to have adverse outcomes than unvaccinated women. The lack of increased adverse outcomes associated with influenza vaccination suggests that the benefits of vaccination during pregnancy to the woman and her child far outweigh any risk, if there is one, from the vaccination."
  • Gastroenteritis - Perinatal Risk Factors Associated With Gastroenteritis Hospitalizations in Aboriginal and Non-Aboriginal Children in Western Australia (2000-2012): A Record Linkage Cohort Study[5] "Gastroenteritis is a leading cause of childhood morbidity worldwide. We aimed to assess the maternal and infant characteristics and population attributable fractions associated with childhood gastroenteritis-related hospitalizations. METHODS: We conducted a whole-of-population retrospective birth cohort study of 367,476 children live-born in Western Australia 2000-2012. ...Given the beneficial effect of infant rotavirus vaccination in preventing all-cause gastroenteritis hospitalization, efforts should be taken to optimize rotavirus vaccine coverage in those at highest risk."
  • intrauterine Growth Restriction Human papillomavirus infection and intrauterine growth restriction: a data-linkage study[6] "Using unbiased population data, to examine whether having a positive Pap smear, and thus a high probability of Human Papilloma Virus (HPV) infection, is a significant risk factor for intrauterine growth restriction (IUGR) in a subsequent pregnancy. CONCLUSIONS: Mothers with a positive Pap smear have an increased risk of IUGR, especially for VLBW, which is independent of other risk factors. The results confirm previous findings in a small study and emphasise the need to consider the risks of both cancer and IUGR in all HPV vaccination programs."
Pregnancy Care Guidelines 2018

This edition brings together the two previous modules and contains updates of a number of topics from them, including weight and body mass index (weight monitoring reviewed), fetal growth and wellbeing, risk of preterm birth, risk of pre-eclampsia (risk factors and prediction reviewed), family violence, hyperglycaemia (early testing reviewed), hepatitis C, thyroid dysfunction, vitamin D status and chromosomal anomalies (cell- free DNA testing reviewed). The new topic substance use has also been incorporated.

See also The Australian Immunisation Handbook 10th edition (2015) Canberra: Australian Government Department of Health. ISBN: 978-1-74241-861-2 Online ISBN: 978-1-74241-862-9..
Aus-Imm-Handbook-2015.jpg

News - Complete human day 14 post-implantation embryo models from naïve Embryonic Stem Cells
Carnegie Stage 6 Embryo
Carnegie Stage 6 Embryo

This recent Nature paper[8] describes the use of naïve human Embryonic Stem Cells to recapitulate the early stages of human development.

"The ability to study human post-implantation development remains limited due to ethical and technical challenges associated with intrauterine development after implantation....only genetically unmodified human naïve human ES cells...recapitulate the organization of nearly all known lineages and compartments of post-implantation human embryos including epiblast, hypoblast, extra-embryonic mesoderm, and trophoblast surrounding the latter layers...These human complete SEMs demonstrated developmental growth dynamics that resemble key hallmarks of post-implantation stage embryogenesis up to 13-14 days post-fertilization (dpf) (Carnegie stage 6a)."

Links: stem cells | Carnegie stage 6
  1. Australian Institute of Health and Welfare 2019. Physical activity during pregnancy 2011–12. Cat. no. PHE 243. Canberra: AIHW. PDF
  2. 2.0 2.1 Papalou O, Kandaraki EA, Papadakis G & Diamanti-Kandarakis E. (2019). Endocrine Disrupting Chemicals: An Occult Mediator of Metabolic Disease. Front Endocrinol (Lausanne) , 10, 112. PMID: 30881345 DOI.
  3. McHugh L, Marshall HS, Perrett KP, Nolan T, Wood N, Lambert SB, Richmond P, Ware RS, Binks P, Binks MJ & Andrews RM. (2019). The Safety of Influenza and Pertussis Vaccination in Pregnancy in a Cohort of Australian Mother-Infant Pairs, 2012-2015: The FluMum Study. Clin. Infect. Dis. , 68, 402-408. PMID: 30475988 DOI.
  4. Getahun D, Fassett MJ, Peltier MR, Takhar HS, Shaw SF, Im TM, Chiu VY & Jacobsen SJ. (2019). Association between seasonal influenza vaccination with pre- and postnatal outcomes. Vaccine , , . PMID: 30799158 DOI.
  5. Fathima P, Snelling TL, de Klerk N, Lehmann D, Blyth CC, Waddington CS & Moore HC. (2019). Perinatal Risk Factors Associated With Gastroenteritis Hospitalizations in Aboriginal and Non-Aboriginal Children in Western Australia (2000-2012): A Record Linkage Cohort Study. Pediatr. Infect. Dis. J. , 38, 169-175. PMID: 29620723 DOI.
  6. Ford JH, Li M, Scheil W & Roder D. (2019). Human papillomavirus infection and intrauterine growth restriction: a data-linkage study. J. Matern. Fetal. Neonatal. Med. , 32, 279-285. PMID: 28889772 DOI.
  7. Department of Health (2018) Clinical Practice Guidelines: Pregnancy Care. Canberra: Australian Government Department of Health. (5 June 2019)
  8. Oldak B, Wildschutz E, Bondarenko V, Comar MY, Zhao C, Aguilera-Castrejon A, Tarazi S, Viukov S, Pham TXA, Ashouokhi S, Lokshtanov D, Roncato F, Ariel E, Rose M, Livnat N, Shani T, Joubran C, Cohen R, Addadi Y, Chemla M, Kedmi M, Keren-Shaul H, Pasque V, Petropoulos S, Lanner F, Novershtern N & Hanna JH. (2023). Complete human day 14 post-implantation embryo models from naïve ES cells. Nature , , . PMID: 37673118 DOI.
Older News Articles  
Older News Articles - Climate Change Abnormal Development | Air Pollution | Rare Sesquizygotic Twinning | Australia's mothers and babies 2017 | Spinal Muscular Atrophy Screening | Australian 2018 Pregnancy Care Guidelines | CRISPR | Ronan O’Rahilly


Objectives

Human Embryonic Development (week 1 to 8)

Applied Embryology: birth statistics, unintended pregnancies, ART, abnormalities statistics, timeline of development, trophoblastic disease, embryonic development, placenta, fetal development, maternal diet, multiple pregnancies.

Teratology: definitions, critical periods, medications, chromosomal abnormalities, environmental factors and infections.

Textbooks

Logo.png Hill, M.A. (2020). UNSW Embryology (20th ed.) Retrieved March 28, 2024, from https://embryology.med.unsw.edu.au
Diagnosis Links: Prenatal Diagnosis | pregnancy test | amniocentesis | chorionic villus sampling | ultrasound | Alpha-Fetoprotein | Pregnancy-associated plasma protein-A | Fetal Blood Sampling | Magnetic Resonance Imaging | Computed Tomography | Non-Invasive Prenatal Testing | Fetal Cells in Maternal Blood | Preimplantation Genetic Screening | Comparative Genomic Hybridization | Genome Sequencing | Neonatal Diagnosis | Category:Prenatal Diagnosis | Fetal Surgery | Classification of Diseases | Category:Neonatal Diagnosis

neonatal diagnosis

Abnormality Links: abnormal development | abnormal genetic | abnormal environmental | Unknown | teratogens | ectopic pregnancy | cardiovascular abnormalities | coelom abnormalities | endocrine abnormalities | gastrointestinal abnormalities | genital abnormalities | head abnormalities | integumentary abnormalities | musculoskeletal abnormalities | limb abnormalities | neural abnormalities | neural crest abnormalities | placenta abnormalities | renal abnormalities | respiratory abnormalities | hearing abnormalities | vision abnormalities | twinning | Developmental Origins of Health and Disease |  ICD-11
Historic Embryology  
1915 Congenital Cardiac Disease | 1917 Frequency of Anomalies in Human Embryos | 1920 Hydatiform Degeneration Tubal Pregnancy | 1921 Anencephalic Embryo | 1921 Rat and Man | 1966 Congenital Malformations
The Developing Human, 10th edn.jpg Moore, K.L., Persaud, T.V.N. & Torchia, M.G. (2015). The developing human: clinically oriented embryology (10th ed.). Philadelphia: Saunders. UNSW Students have online access to the current 10th edn. through the UNSW Library subscription.
Larsen's human embryology 5th ed.jpg Schoenwolf, G.C., Bleyl, S.B., Brauer, P.R., Francis-West, P.H. & Philippa H. (2015). Larsen's human embryology (5th ed.). New York; Edinburgh: Churchill Livingstone. UNSW Students have online access to the current 5th edn. through the UNSW Library subscription.

Applied Embryology

Australia’s mothers and babies - in brief 2016 (published 2018).[1]


The data below is based the 2015 data[2] and will be updated to the more recent 2016 data (published 2018). Earlier report data summaries are also available.[3][4][5][6][7][8][9]

This data should help you as a clinician and researcher to understand the current trends in reproductive medicine within Australia. Also see recent general population data in Australian Statistics.

  • 2015 - 306,725 live births and 2,160 (less than 1%) were stillbirth and perinatal death
  • 2014 - 307,844 live births and 2,200
  • 2013 - 307,277 live births and 2,191
  • 2012 - 312,153 live births and 2,255
  • 2011 - 301,810 live births and 2,220
  • 2009 - 296,791 live births and 2,341
  • 2008 - 294,737 live births and 2,188
  • 2007 - 292,027 live births and 2,177
  • Congenital abnormalities are the leading cause of perinatal deaths (fetal+neonatal)
Australian-births 2011.jpg

Mothers

Mothers - 2015  

304,268 women gave birth in Australia — an increase of 13% since 2005 (267,795 women).

Rate of women giving birth 62 per 1,000 women of reproductive age (15–44 years)

  • rate has declined from a peak of 66 per 1,000 women in 2007.
  • rate has fluctuated between 2005 and 2015

Average age of all women who gave birth continues to rise and was 30.3, compared with 29.7 in 2005.

  • The median age was slightly higher, at 31 years in 2015.

The average age has also increased for Aboriginal and Torres Strait Islander mothers, from 24.9 in 2005 to 25.6 in 2015, with a median of 25 years.

The proportion of mothers aged 35 and over has increased from 20% in 2005 to 22% (See also USA Data)

The proportion of mothers aged under 25 has decreased from 19% to 15%.

The average age of first‐time mothers also increased, from 28.1 in 2005 to 28.9

Multiple pregnancies - represented 1.5% of all pregnancies.

  • Almost all multiple pregnancies (98%) was twinning (dizygotic, monozygotic)
  • Small proportion (2%) were other multiples (triplets, quadruplets or higher).
Maternal Conditions
  • smoking - One in 10 mothers (31,268 or 10%) who gave birth in 2015 smoked at some time during their pregnancy, a decrease from 11% in 2014 and 15% in 2009.
  • hypertension - 8 per 1,000 mothers had chronic hypertension and 37 per 1,000 had gestational hypertension (preeclampsia)
  • maternal diabetes - 11 per 1,000 had pre‐existing diabetes and 94 per 1,000 had gestational diabetes. (2014 - 10 per 1,000 and 83 per 1,000).
Birth - cephalic presentations.jpg

Birth - cephalic presentations

USA mean age of mother 1970- 2010 graph.png

USA mean age of mother (1970-2010)

Babies

Babies  
Gestational Age
  • average gestational age for all babies was 38.6 GA weeks
  • 91 % born at term (37–41 GA weeks)
  • most births occurred in October, September and July

Pre-term Birth

  • 8.6 % born pre‐term (most between 32 and 36 weeks) (8.3 % 2013)
    • 7.9 % NSW (NSW Report NSW Health Statistics)
    • higher in - multiple births, indigenous mothers, smokers, remote areas, very young (under 20) and older mothers (40+)
  • less than 1% born post‐term (42 weeks and over)

USA births by gestational age 1990-2006 graph.png

Birth Weight
  • mean birthweight 3,327 grams
  • 92% (282,530) normal birthweight range
  • 1.4% (4,263) high birthweight (4,500+ grams)
  • 6.5% (19,852) low birthweight (less than 2,500 grams)
    • 81 % stillborn low birthweight
Apgar Score
Apgar score of 7 or more
  • 98% all liveborn babies
  • 92% pre-term babies
  • 92% low birthweight babies (less than 2,500 grams)
  • 1 in 5 liveborn babies require active resuscitation
Special care nurseries (SCN) or neonatal intensive care units (NICU) Admissions
  • 16% (43,348) all Iiveborn babies (2015 - 15%)
  • 74% Pre-term babies
  • majority of multiple births are pre-term
  • 1.5 times more indigenous babies

SCN-NCIU-AUS2015 graph.jpg

stillbirth and perinatal death perinatal mortality
2013 and 2014 - 622,037 babies were born in Australia and 6,037 of those babies died in the perinatal period
  • 4,419 stillbirths and 1,618 neonatal deaths
  • perinatal mortality rate was 9.7 per 1,000 births
  • stillbirth (fetal mortality) rate was 7.1 per 1,000 births
  • neonatal mortality rate 2.6 per 1,000 live births.
  • Between 1995 and 2014 there has been some reduction in neonatal mortality rate, but the stillbirth rate has remained relatively unchanged.

Caesarean rates 1990-2014.jpg

Self-Directed Learning 1


2013 National core maternity indicators  
National core maternity indicators 2013.jpg

2013 National core maternity indicators[10]

This report provides a baseline for monitoring changes in the quality of maternity services across Australia using 10 national core maternity indicators.

  1. Smoking in pregnancy for all women giving birth
  2. Antenatal care in the first trimester for all women giving birth
  3. Episiotomy for women having their first baby and giving birth vaginally
  4. Apgar Score of less than 7 at 5 minutes for births at or after term
  5. Induction of labour for selected women giving birth for the first time
  6. Caesarean section for selected women giving birth for the first time
  7. Normal (non-instrumental) vaginal birth for selected women giving birth for the first time
  8. Instrumental vaginal birth for selected women giving birth for the first time
  9. General anaesthetic for women giving birth by caesarean section
  10. Small babies among births at or after 40 weeks gestation
  • National rates have decreased for smoking in pregnancy, episiotomy among women having their first baby and giving birth vaginally and the proportion of babies born weighing less than 2,750 grams at or after 40 weeks.
  • However for some indicators, including induction of labour, caesarean section and instrumental vaginal birth, rates have increased and point to areas for possible further attention.

Unintended Pregnancy

A recent 2018 USA study[11] of Unintended pregnancy and interpregnancy interval by maternal age, National Survey of Family Growth.


  • 40% of pregnancies were unintended
  • 36% followed an interpregnancy interval (IPI) less than 18 months.
  • Within each maternal age group, the percentage of pregnancies that were unintended decreased as IPI increased.


Unintended pregnancy is either mistimed (woman wanted to be pregnant later) or unwanted (did not want to ever be pregnant).


Australian Teenage Pregnancy Statistics (2015) AIHW

Australian teenage mothers and birth rate 2015.jpg

  • Rate of teenage births in Australia is in decline, from 17.5 births per 1,000 women in 2005 to 11.4 in 2015
  • Babies of teenage mothers were 1.3 times as likely to be of low birthweight than babies of 20-24 year old mothers
  • Babies of teenage mothers were 1.2 times as likely to be preterm than babies of 20-24 year old mothers
  • 1 in 4 teenage mothers smoked after 20 weeks of pregnancy


Unintended and Teen Pregnancy  
2001 USA - Approximately one-half of pregnancies in the United States were unintended (Finer 2006, Perspectives on Sexual and Reproductive Health).

An earlier 1995 USA National Survey of Family Growth (NSFG) found:

  • 49% of pregnancies in the USA (excluding miscarriages)
  • 31% of pregnancies resulting in a live birth are unintended
Teen pregnancy USA.png
A recent Canadian retrospective study[12] of half a million births comparing pregnant women < 20 years of age (adolescent) were compared with those of women 20 to 35 years old.
  • Adolescents had a higher rate of smoking and substance use than adult women and were within the lowest education and family income quintiles.
  • Adolescents had a significantly lower risk of gestational hypertension, gestational diabetes, placental abruption, and placenta previa, but their risk of preterm premature rupture of membranes was significantly higher.
  • Neonates with an adolescent mother had significantly higher risks of admission to NICU and very preterm birth.
  • There was no significant difference between the two groups in rates of small for gestational age babies, low birth weight, preterm birth, and fetal death.
Self-Directed Learning 2

Links: CDC Unintended Pregnancy Prevention | Pregnancy Risk Assessment Monitoring System USA | The Measurement and Meaning of Unintended Pregnancy

Assisted Reproduction Technology

Assisted reproductive technology in Australia and New Zealand 2015

Assisted Reproduction Technology (ART) is also sometimes also used to identify In vitro fertilization (IVF) but now includes many new techniques. Assisted reproductive technology (ART) is a group of procedures that involve the in vitro (outside of body) handling of human oocytes (eggs) and sperm or embryos for the purposes of establishing a pregnancy. Each ART treatment involves a number of stages and is generally referred to as an ART treatment cycle. The embryos transferred to a women can either originate from the cycle in which they were created (fresh cycle) or be frozen and thawed before transfer (thaw cycle).

Assisted Reproductive Technology in Australia and New Zealand (2015)[13]

  • 77,721 ART treatment cycles reported from Australian and New Zealand clinics in 2015 (71,479 and 6,242 respectively)
    • 5.6% increase in Australia and 6.0% increase in New Zealand on 2014.
    • 14.4 cycles per 1,000 women of reproductive age (15–44 years) in Australia
    • 94.5% autologous cycles (own oocytes or embryos)
    • 37.4% autologous frozen and thawed
    • 39,006 women who undertook 73,481 autologous fresh and/or thaw cycles
    • Over the last five years there has been an increasing trend in the proportion of cycles where all oocytes or embryos are cryopreserved for potential future use from (2011) 5.0% (2015) 17.2%
  • 35.8 years - average age of women undergoing autologous cycles
    • 40.6 years - average age of women undergoing ART treatment using donor oocytes or embryos
    • 24.8% were aged 40 or older. The average age of the male partner of the women undergoing autologous and recipient cycles was ** 38.1 years - average age of the male partner
  • 22.8% (17,726) resulted in a clinical pregnancy
  • 18.1% (14,040) in a live delivery
    • higher live delivery rate in younger women.
      • under 30 - live delivery rate per embryo transfer 38.4% for autologous fresh cycles and 32.6% for autologous thaw cycles
      • women aged over 44 - live delivery rate was 0.7% per embryo transfer for autologous fresh and 7.6% thaw cycles.
  • 14,791 babies born (including 14,655 liveborn babies)
    • 78.8% were full-term singletons of normal birthweight.
  • shift from cleavage stage transfers to blastocyst transfers (from 57.7% in 2011 to 73.5% in 2015)
  • increase in vitrification as a cryopreservation method (from 73.0% of thaw blastocyst transfer cycles in 2011 to 86.1% in 2015).
  • intracytoplasmic sperm injection (ICSI) has remained stable at around 63% of embryo transfer cycles in 2011-2015.
  • 36% decrease in Multiple births from 6.9% in 2011 to 4.4% in 2015.



Australia 2013 Data
  • 71,516 ART treatment cycles reported from Australian and New Zealand clinics in 2013 (66,143 and 5,373 respectively).
    • 1.9% increase in Australia and 3.8% increase in New Zealand on 2012.
  • 13.7 cycles per 1,000 women of reproductive age (15–44 years) in Australia
    • compared with 5.9 cycles per 1,000 women of reproductive age in New Zealand.
  • 95.1% autologous cycles (womens own oocytes or embryos)
    • 36.6% autologous cycles embryos frozen and thawed.
    • 37,192 women who undertook 67,980 autologous fresh and/or thaw cycles in Australia and New Zealand
  • 1.8 average fresh and/or thaw cycles per woman were undertaken
    • more cycles per woman in Australia (1.9 cycles per woman) than in New Zealand (1.5 cycles per woman).
  • Preimplantation Genetic Diagnosis (PGD) was performed in 2,740 cycles (19.4% increase), 4.4% of cycles in which embryos were created or thawed.
Australia 2012 Data
Assisted reproductive technology in Australia and New Zealand 2012.jpg

The following data from previous year

  • 70,082 assisted reproductive technology (ART) treatment cycles performed in Australia (64,905 ) and New Zealand (5,177),
  • 3,590 babies born (including 13,312 liveborn babies) following ART treatment in 2012.
  • an increase of 5.8% for Australia and a decrease of 0.2% for New Zealand on 2011.
  • 13.7 cycles per 1,000 women of reproductive age (15–44 years) in Australia
  • Women used their own oocytes or embryos (autologous) in 95.2% of treatments, and 34.8% of all cycles used frozen/thawed embryos.
  • 36,171 women who undertook 66,710 autologous fresh and/or thaw cycles in Australia and New Zealand in 2012.
  • average, 1.8 cycles per woman were undertaken in 2012, with more cycles per woman in Australia (1.9 cycles per woman) than in New Zealand (1.5 cycles per woman).
  • increase in cycles where preimplantation genetic diagnosis was performed, from 2.0% of cycles in 2011 to 3.7% of cycles in 2012.
  • Maternal Age
    • women aged under 30, the live delivery rate was 26.0% for both autologous fresh and thaw cycles.
    • women aged over 44, the live delivery rate was 0.9% and 4.6% for autologous fresh and thaw cycles respectively.

Assisted reproductive technology in Australia and New Zealand 2012[14] Nov 2014

USA 2013 Data
ART USA (2013)
  • 6.9 million (11%) of the 61 million women aged 15–44 years had received infertility services at some time in their lives.
  • 93,787 fresh nondonor ART cycles were started in 2013.
  • 33,425 (36%) led to a pregnancy, but only 27,406 (29%) resulted in a live birth.
  • 6,019 (almost 1 in 5) of ART pregnancies did not result in a live birth.


Links: Assisted Reproductive Technology
Self-Directed Learning 3

Early Development Issues

Abnormal Implantation

Ectopic Implantation (Pregnancy)

Ectopic tubal pregnancy
Abnormal implantation sites or Ectopic Pregnancy occurs if implantation is in uterine tube or outside the uterus.
  • sites - external surface of uterus, ovary, bowel, gastrointestinal tract, mesentry, peritoneal wall
  • If not spontaneous then, embryo has to be removed surgically

Tubal pregnancy - 94% of ectopic pregnancies

  • if uterine epithelium is damaged (scarring, pelvic inflammatory disease)
  • if zona pellucida is lost too early, allows premature tubal implantation
  • embryo may develop through early stages, can erode through the uterine horn and reattach within the peritoneal cavity
Ectopic 01.jpg
 ‎‎Ectopic Pregnancy
Page | Play

This is also the most common cause of pregnancy-related deaths in the first trimester. A United Kingdom enquiry into maternal deaths[15], identified ectopic pregnancy as the fourth most common cause of maternal death (73% of early pregnancy deaths).

Hydatidiform Mole

Hydatidiform Mole

Another type of abnormality is when only the conceptus trophoblast layers proliferates and not the embryoblast, no embryo develops, this is called a "hydatidiform mole", which is due to the continuing presence of the trophoblastic layer, this abnormal conceptus can also implant in the uterus. The trophoblast cells will secrete human chorionic gonadotropin (hCG), as in a normal pregnancy, and may appear maternally and by pregnancy test to be "normal". Prenatal diagnosis by ultrasound analysis demonstrates the absence of a embryo.

There are several forms of hydatidiform mole: partial mole, complete mole and persistent gestational trophoblastic tumor. Many of these tumours arise from a haploid sperm fertilizing an egg without a female pronucleus (the alternative form, an embryo without sperm contribution, is called parthenogenesis). The tumour has a "grape-like" placental appearance without enclosed embryo formation. Following a first molar pregnancy, there is approximately a 1% risk of a second molar pregnancy.

This topic is also covered in Placenta - Abnormalities

Twinning

  • Twin deliveries and place of birth in NSW 2001-2005[16] "Both infant and maternal morbidity increase from 39 weeks gestation. Delivery of twins before 36 weeks at smaller hospitals (< 500 deliveries per annum) should be avoided. A twin pregnancy where there is a greater or equal to 20% difference in estimated fetal weights should be considered for referral to a tertiary obstetric unit."

Dizygotic Twinning

Dizygotic twins (fraternal, non-identical) arise from separate fertilization events involving two separate oocyte (egg, ova) and spermatozoa (sperm). Dizygotic twinning can be increased by Assisted Reproductive Technologies (ART) that use double embryo transfer techniques.

Monoygotic Twinning

Monoygotic twins (identical) produced from a single fertilization event (one fertilised egg and a single spermatazoa, form a single zygote), these twins therefore share the same genetic makeup. Occurs in approximately 3-5 per 1000 pregnancies, more commonly with aged mothers. The later the twinning event, the less common are initially separate placental membranes and finally resulting in conjoined twins.

Week Week 1 (GA week 3) Week 2 (GA week 4)
Day 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14
Cell Number 1 1 2 16 32 128 bilaminar
Event Ovulation Fertilization First cell division Morula Early blastocyst Late blastocyst

Hatching

Implantation starts X inactivation
Follicle 001 icon.jpg Early zygote.jpg Human embryo day 2.jpg Human embryo day 3.jpg Human embryo day 5.jpg CSt3.jpg Week2 001 icon.jpg Macaque Xi at interphase 02.jpg
Monoygotic

Twin Type

Diamniotic

Dichorionic

Diamniotic

Monochorionic

Monoamniotic

Monochorionic

Conjoined

Table based upon recent a recent twinning review.[17]   Links: twinning

Links: Twinning


Self-Directed Learning 4

Abnormal Development

Australian abnormalities by System
Australian abnormalities by System

Embryological development is a robust biological system able to cope with many stresses without long-term consequences. When development does go wrong there are generally 3 major types groups: Genetic (inherited), Environmental (maternal) derived and Unknown (not determined or known) abnormalities. Also often not considered, is that pregnancy itself can also expose abnormalities in the mother (congenital heart disease, diabetes, reproductive disorders) that until the pregnancy had gone undetected.

Genetic abnormalities in medicine are still mainly about determining a family history and good prenatal/neonatal diagnosis. Realise that there exists in all of us genetic variations and some variations which eventually expand be expressed as a genetic disorder (CAG expansions).

Abnormality Links
Abnormality Links: abnormal development | abnormal genetic | abnormal environmental | Unknown | teratogens | ectopic pregnancy | cardiovascular abnormalities | coelom abnormalities | endocrine abnormalities | gastrointestinal abnormalities | genital abnormalities | head abnormalities | integumentary abnormalities | musculoskeletal abnormalities | limb abnormalities | neural abnormalities | neural crest abnormalities | placenta abnormalities | renal abnormalities | respiratory abnormalities | hearing abnormalities | vision abnormalities | twinning | Developmental Origins of Health and Disease |  ICD-11
Historic Embryology  
1915 Congenital Cardiac Disease | 1917 Frequency of Anomalies in Human Embryos | 1920 Hydatiform Degeneration Tubal Pregnancy | 1921 Anencephalic Embryo | 1921 Rat and Man | 1966 Congenital Malformations

Prenatal diagnosis are the clinical tools used to determine both normal and abnormal development. There are a growing number of new diagnostic techniques that are being applied to human embryonic development.

Prenatal Diagnosis Links
Diagnosis Links: Prenatal Diagnosis | pregnancy test | amniocentesis | chorionic villus sampling | ultrasound | Alpha-Fetoprotein | Pregnancy-associated plasma protein-A | Fetal Blood Sampling | Magnetic Resonance Imaging | Computed Tomography | Non-Invasive Prenatal Testing | Fetal Cells in Maternal Blood | Preimplantation Genetic Screening | Comparative Genomic Hybridization | Genome Sequencing | Neonatal Diagnosis | Category:Prenatal Diagnosis | Fetal Surgery | Classification of Diseases | Category:Neonatal Diagnosis
NIPT - Non-Invasive Prenatal Testing
Fetal aneuploidy screening with cell-free DNA in late gestation[18]"The aim of this study was to evaluate clinical use of NIPT at gestational ages of 23 weeks and above. A cohort of 5579 clinical patients with singleton gestations of 23 weeks or greater submitting a blood sample for NIPT in an 18-month period were selected for this study. ...Of 5372 reported late-gestation samples, 151 (2.8%) were reported as aneuploidy detected or suspected. In late-gestation samples, the overall observed positive predictive value (PPV) for NIPT was 64.7%, with an observed PPV of 100% in the subset of cases with multiple clinical indications including abnormal ultrasound findings. NIPT is a highly accurate prenatal screening option for women after 23 weeks of gestation. Women who presented for NIPT in the latter stages of pregnancy more frequently specified clinical indications of abnormal ultrasound findings than women who entered screening earlier in pregnancy."

More? Fetal Cells in Maternal Blood | RACGP | NCHPEG

While genetic abnormalities will have well-defined impacts upon development, environmentally derived effects can be harder to define and often variable depending on many different factors (timing, exposure level, and the combination effects with other factors). This combination effect can also be seen between genetic and environmental interacting to give an even broader spectrum of both major and minor abnormalities.

Environmental Links
Environmental Links: Introduction | low folic acid | iodine deficiency | Nutrition | Drugs | Australian Drug Categories | USA Drug Categories | thalidomide | herbal drugs | Illegal Drugs | smoking | Fetal Alcohol Syndrome | TORCH | viral infection | bacterial infection | fungal infection | zoonotic infection | toxoplasmosis | Malaria | maternal diabetes | maternal hypertension | maternal hyperthermia | Maternal Inflammation | Maternal Obesity | hypoxia | biological toxins | chemicals | heavy metals | air pollution | radiation | Prenatal Diagnosis | Neonatal Diagnosis | International Classification of Diseases | Fetal Origins Hypothesis
Bacterial Links: bacterial infection | syphilis | gonorrhea | tuberculosis | listeria | salmonella | TORCH | Environmental | Category:Bacteria
Viral Links: viral infection | TORCH | cytomegalovirus | hepatitis | HIV | parvovirus | polio | rubella virus | chickenpox | Lymphocytic Choriomeningitis Virus | Zika virus | human papillomavirus | rotavirus | West Nile virus | varicella virus | vaccination | zoonotic infection | environment
Historic Embryology - Viral 
1941 Rubella Cataracts | 1944 Rubella Defects

International Classification of Diseases

The International Classification of Diseases (ICD) World Health Organization's classification used worldwide as the standard diagnostic tool for epidemiology, health management and clinical purposes. This includes the analysis of the general health situation of population groups. It is used to monitor the incidence and prevalence of diseases and other health problems. Within this classification "congenital malformations, deformations and chromosomal abnormalities" are (Q00-Q99) but excludes "inborn errors of metabolism" (E70-E90).


ICD-10

Australian Birth Anomalies System

"The national collation and reporting of birth anomalies data has been suspended in recent years due to concerns about data quality and comparability."
  • Variability among states and territories in scope of birth anomalies data collections: sources of birth anomalies notifications and definitions and classifications used; method of data collection and available resources.
  • Variability among the states and territories in the timing and method of the provision of birth anomalies data to the AIHW National Perinatal Statistics Unit (NPSU) for national collation and reporting.
  • New Australian Birth Anomalies System should be data for birth anomalies detected up to 1 year of age
    • including data on terminations of pregnancies with birth anomalies and regardless of gestational age (i.e. including less than 20 weeks gestation)
  • System will initially be based on data from the states able to detect birth anomalies at least up to 1 year of age (NSW, VIC, WA and SA), further extending the period of detection in the future.
  • Congenital anomalies are coded using the British Paediatric Association Classification of Diseases (ICD-9-BPA), based on the International Classification of Diseases, 9th Revision (ICD-9).
The Australian Congenital Anomalies Monitoring System (ACAMS) supersedes the National Congenital Malformations and Birth Defects Data Collection (NCM&BD).
Congenital Anomalies in Australia 2002-2003  
Congenital anomalies in Australia 2002-2003[19] was published in 2008 as part a new revised series on 33 selected congenital anomalies also monitored internationally by the International Clearinghouse of Birth Defects Surveillance and Research.
  • Hypospadia is the most commonly reported condition at birth, but severity of the condition is not reported to the national data collection.
  • Trisomy 21 (Down’s syndrome) is the next most commonly reported condition at birth (11.1 per 10,000 births), but many affected pregnancies are detected early and managed by early termination. An estimated 63.6% of the fetuses diagnosed with trisomy 21 were managed by terminations of pregnancy or were fetal deaths. When terminations of pregnancy were included, the estimated rate for trisomy 21 was 26.3 per 10,000 pregnancies. Trisomy 21 was more common with advancing maternal age.
    • Other chromosomal abnormalities such as trisomy 13 and trisomy 18 also had a large proportion of fetal deaths or terminations of pregnancy and were more common in women aged 40 years or older.
  • Neural tube defects were diagnosed in about 4.2 per 10,000 births.
  • More males than females diagnosed with congenital anomalies for many of the reported conditions (e.g. hydrocephalus, most of the reported congenital heart diseases, oesophageal atresia and polycystic kidneys).
  • Anencephaly - younger women had a higher rate compared with older women, most of the women who gave birth to a baby with anencephaly (77.2%) were in the 20–34 years age group.
Links: Human Abnormal Development | Hypospadia | Trisomy 21 | Trisomy 13 Trisomy 18 | Neural Tube Defects | Folic Acid and Neural Tube Defects | Hydrocephalus | Cardiovascular Abnormalities | Polycystic Kidney Disease | Anencephaly | Australian Statistics | Reports
External Links Notice - The dynamic nature of the internet may mean that some of these listed links may no longer function. If the link no longer works search the web with the link text or name. Links to any external commercial sites are provided for information purposes only and should never be considered an endorsement. UNSW Embryology is provided as an educational resource with no clinical information or commercial affiliation.
External Links: AIHW Report Page | NPESU Report Page | International Clearinghouse of Birth Defects Surveillance and Research

Links: Australian Congenital Anomalies Monitoring System | Congenital Anomalies in Australia 2002-2003

NSW Data

Congenital Conditions Register

Scheduled congenital conditions (section 2) detected during pregnancy or in infants up to one year of age in NSW are required to be reported under the NSW Public Health Act 1991.

Scheduled congenital conditions include:

  1. All structural malformations. Examples include spina bifida, microcephaly, transposition of the great vessels, ventricular septal defects, pulmonary agenesis, polycystic lungs, duodenal atresia, exomphalos, hypospadias, cleft lip/palate, microphthalmia, limb reductions, polydactyly, birthmarks greater than 4 cms diameter, cystic hygroma and multisystem syndromes including at least one structural malformation.
  2. Chromosomal abnormalities. Examples include Down syndrome and unbalanced translocations.
  3. Four medical conditions: cystic fibrosis, phenylketonuria, congenital hypothyroidism and thalassaemia major.

Congenital conditions that are not notifiable include:

  1. Minor anomalies occurring in isolation (Examples of minor anomalies include skin tags, deviated nasal septum, tongue tie, benign heart murmurs, clicky non-dislocating hips, sacral dimples, positional talipes, abnormal palmar creases, dysmorphic features).
  2. Birth injuries.
  3. Congenital infections which do not result in a structural malformation.
  4. Tumours and cysts.
  5. Conditions arising from prematurity or asphyxiation.


Links: NSW Health - Congenital Conditions Register - Reporting Requirements 2012 | PDF


NSW Mothers and Babies Report 2015

New South Wales Mothers and Babies 2015 cover
New South Wales Mothers and Babies 2015
NSW Perinatal Data Collection form
NSW Perinatal Data Collection form

NSW is one of the largest states in Australia by population. The New South Wales Perinatal Data Collection (PDC) is a population-based surveillance system covering all births in NSW public and private hospitals, as well as home births. It encompasses all live births, and stillbirths of at least 20 weeks gestation or at least 400 grams birth weight.[20]

  • Number of births decreased from 97,245 in 2011 to 96,391 in 2015 (decrease of 0.9%).
  • Percentage of teenage mothers fell from 3.2% in 2011 to 2.5% in 2015.
  • Rate of normal vaginal birth decreased from 56.9% in 2011 to 56.0% in 2015.
  • Operative and instrumental births were more common among privately than publicly insured mothers.
  • Proportion of smoking mothers during pregnancy declined from 11.1% in 2011 to 8.9% in 2015.
  • Majority of mothers planned to give birth in a hospital labour ward
    • 87% per cent of mothers who planned to give birth in a birth centre actually did so.
    • There were 187 homebirths in NSW reported in 2015.
  • Premature babies (less than 37 weeks gestation) 7.9% (slight increase from 7.5% in 2011).
  • Since 2011, the rate of low birth weight (less than 2,500 grams) has remained stable, ranging from 6.1% to 6.6%.
    • Low birth weight rate was 6.6% in 2015.
  • Between 2011 and 2015, the reported number of Aboriginal or Torres Strait Islander mothers giving birth increased from 2,975 to 3,823, an increase from 3.1% to 4.0% of all mothers.
  • Aboriginal or Torres Strait Islander
    • teenage mothers fell from 19.0% in 2011 to 15.4% in 2015.
    • 45.0% of Aboriginal or Torres Strait Islander mothers reported smoking during pregnancy.
    • Since 2011, rates of low birth weight and prematurity in Aboriginal or Torres Strait Islander babies has been over 11%. In 2015, 11.3% of Aboriginal or Torres Strait Islander babies were low birth weight and 12.7% were premature.
    • Perinatal mortality rate of 9.6 per 1,000 births in Aboriginal or Torres Strait Islander mothers in 2015 is higher than the rate of 8.1 per 1,000 births experienced among babies born to non-Aboriginal or Torres Strait Islander mothers.


Victoria - 10 most reported birth anomalies  
Based upon statistics from the Victorian Perinatal Data Collection Unit in Victoria between 2003-2004.
Hypospadia hypospadias (More? External Genital Male Development Movie)
Obstructive Defect of the Renal Pelvis Obstructive Defects of the Renal Pelvis (obstructive defects of the renal pelvis, uteropelvic junction obstruction, pelvo-uterero junction obstruction) Term describing a developmental renal abnormality due to partial or complete blockage of the drainage of the kidney pelvis requiring surgical correction. The blockage can also have several causes including: unusual ureter twisting or bending, ureter compression by a blood vessel, malformations of the muscular wall. The blockage leads to an accumulation of urine in the affected region, with several potential effects: nephron damage from compression (hydronephrosis); decreased urine output leading to lack of amniotic fluid (oligohydramnios); respiratory development effects due to the lack of amniotic fluid.
  • The most common type of obstruction is at the uteropelvic junction (UPJ), between the junction of the ureter and the kidney.
  • Blockage lower as the ureter enters the bladder, the ureterovesicular junction (UVJ), usually involves only one kidney and the back flow enlarges the affected ureter (megaureter).

(More? renal abnormalities | renal)

Ventricular Septal Defect ventricular septal defect (More? ventricular septal defect)

Basic Heart Development Timeline.jpg

Heart Development Timeline (see Basic Cardiac Embryology)

Congenital dislocation hip Developmental dysplasia of the hip or Congenital Dislocated Hip

(Developmental dysplasia of the hip (DDH), congenital hip dislocation, congenital hip dysplasia) Term describes a spectrum of musculoskeletal disorders of hip instability due either to the femoral head being able to move outside the acetabulum (luxation or dislocation), or abnormally within the acetabulum (subluxation or partial dislocation). This includes presentation following a normal examination of the hips in the newborn period (Ortolani and Barlow tests). When detected can be managed with splinting (Denis-Browne splint) allows the hip joint to develop normally and does not require surgery. If undetected and left untreated, the hip joint develops abnormally and surgical reduction is required. (More? Pelvis Development)

Trisomy 21 male Trisomy 21 or Down syndrome - The most common genetic abnormality. (More? Trisomy 21)
Hydrocephalus MRI hydrocephalus rapid increase in head circumference or an unusually large head size due to excessive accumulation of cerebrospinal fluid in the brain.(More? hydrocephalus | Neural Abnormalities | NINDS - Hydrocephalus Fact Sheet | Hydrocephalus Support Association | USA National Hydrocephalus Foundation)
Cleft palate cleft palate - The palate separates the nasal cavity from the oral cavity, the abnormality has many different causes, and occurs more frequently in females (57%) than in males (43%). (More? cleft palate)
Trisomy 18 male Trisomy 18 or Edward Syndrome - multiple abnormalities of the heart, diaphragm, lungs, kidneys, ureters and palate 86% discontinued (More? Trisomy 18)
Renal Agenesis/Dysgenesis - reduction in neonatal death and stillbirth since 1993 may be due to the more severe cases being identified in utero and being represented amongst the increased proportion of terminations (approximately 31%). (More? Renal Abnormalities - Renal Agenesis)
Bilateral cleft palate cleft lip and palate - occur with another defect in 33.7% of cases.(More? cleft lip and palate)
Links: Human Abnormal Development | Australian Statistics | Victoria 2004 | USA 2006 | Europe 2010
USA Statistics
USA Selected Abnormalities (CDC National estimates for 21 selected major birth defects 2004–2006)  
Birth Defects Cases per Births (1 in ...) Estimated Annual Number of Cases
anencephaly 4,859 859
spina bifida without anencephaly 2,858 1,460
encephalocele 12,235 341
Anophthalmia/microphthalmia 5,349 780
patent ductus arteriosus‎/common truncus 13,876 301
transposition of the great vessels 3,333 1,252
Tetralogy of Fallot 2,518 1,657
atrial septal defects/ventricular septal defects 2,122 1,966
hypoplastic left heart 4,344 960
cleft palate without cleft lip 1,574 2,651
cleft lip with and without cleft palate 940 4,437
Esophageal atresia/tracheoesophageal fistula 4,608 905
Rectal and large intestinal atresia/stenosis 2,138 1,952
Reduction deformity, upper limbs 2,869 1,454
Reduction deformity, lower limbs 5,949 701
gastroschisis 2,229 1,871
omphalocele 5,386 775
Diaphragmatic hernia 3,836 1,088
Trisomy 13 7,906 528
Trisomy 21 (Down syndrome) 691 6,037
Trisomy 18 3,762 1,109
Links: Human Abnormal Development | CDC Birth Defects - Data & Statistics | USA Statistics | Victoria 2004 | USA 2006 | Europe 2010
European Statistics
Malformation (non-chromosomal) Total Cases Cases Prenatally Diagnosed % of Total Cases
All Anomalies 75751 22573 30
Anencephalus and similar 1232 1185 96
Spina Bifida 1577 1288 82
Hydrocephalus 1914 1403 73
Transposition of great vessels 1188 454 38
Hypoplastic left heart 888 624 70
Cleft lip with or without palate 2857 1379 48
Diaphragmatic hernia 893 509 57
Gastroschisis 993 904 91
Omphalocele 730 596 82
Bilateral renal agenesis including Potter syndrome 392 343 88
Posterior urethral valve and/or prune belly 291 234 80
Limb reduction 1626 811 50
Club foot - talipes equinovarus 3678 1398 38
Malformation (chromosomal)
Chromosomal 12479 8765 70
Down Syndrome 7233 4538 63
Patau syndrome/trisomy 13 685 625 91
Edwards syndrome/trisomy 18 1709 1537 90
Data: EUROCAT Website Database data uploaded 04/12/2012
Links: Human Abnormal Development | Australian Statistics | Victoria 2004 | USA 2006 | Europe 2010


Genetic

Links: Abnormal Development - Genetic
Self-Directed Learning 5

Teratology

Prenatal Screening

Amniocentesis

How and why do things go wrong in development?

These notes cover abnormalities that can occur during development often described as congenital defects or birth defects. There are many different ways that developmental abnormalities can occur the 3 major types are Genetic (inherited), Environmental (maternal) and Unknown (not determined) derived abnormalities. The environmental factors that cause or lead to any of these abnormalities are described as Teratogens.

Diagnosis Links: Prenatal Diagnosis | pregnancy test | amniocentesis | chorionic villus sampling | ultrasound | Alpha-Fetoprotein | Pregnancy-associated plasma protein-A | Fetal Blood Sampling | Magnetic Resonance Imaging | Computed Tomography | Non-Invasive Prenatal Testing | Fetal Cells in Maternal Blood | Preimplantation Genetic Screening | Comparative Genomic Hybridization | Genome Sequencing | Neonatal Diagnosis | Category:Prenatal Diagnosis | Fetal Surgery | Classification of Diseases | Category:Neonatal Diagnosis
Ultrasound
Ultrasound
Ectopic 01.jpg
 ‎‎Ectopic Pregnancy
Page | Play
Cleft lip 01.jpg
 ‎‎Cleft Lip 18 Week
Page | Play
Cleft lip 02.jpg
 ‎‎Cleft Lip 15 Week
Page | Play
Gastroschisis 01.jpg
 ‎‎Gastroschisis
Page | Play

Now consider the terms used to describe the different environmental effects that can occur during pregnancy that may influence outcomes.

  • Teratogen (Greek, teraton = monster) any agent that causes a structural abnormality (congenital abnormalities) following fetal exposure during pregnancy. The overall effect depends on dosage and time of exposure.
  • Absolute risk the rate of occurrence of an abnormal phenotype among individuals exposed to the agent. (e.g. fetal alcohol syndrome)
  • Relative risk the ratio of the rate of the condition among the exposed and the nonexposed. (e.g. smokers risk of having a low birth weight baby compared to non-smokers) A high relative risk may indicate a low absolute risk if the condition is rare.
  • Mutagen a chemical or agent that can cause permanent damage to the deoxyribonucleic acid (DNA) in a cell. DNA damage in the human egg or sperm may lead to reduced fertility, spontaneous abortion (miscarriage), birth defects and heritable diseases.
  • Fetotoxicant is a chemical that adversely affects the developing fetus, resulting in low birth weight, symptoms of poisoning at birth or stillbirth (fetus dies before it is born).
  • Synergism when the combined effect of exposure to more than one chemical at one time, or to a chemical in combination with other hazards (heat, radiation, infection) results in effects of such exposure to be greater than the sum of the individual effects of each hazard by itself.
  • Toxicogenomics the interaction between the genome, chemicals in the environment, and disease. Cells exposed to a stress, drug or toxicant respond by altering the pattern of expression of genes within their chromosomes. Based on new genetic and microarray technologies.

Teratogens

  • Infections, collectively grouped under the acronym TORCH for Toxoplasmosis, Other organisms (parvovirus, HIV, Epstein-Barr, herpes 6 and 8, varicella, syphilis, enterovirus) , Rubella, Cytomegalovirus and Hepatitis. See also the related topics on maternal hyperthermia and bacterial infections. (More? Postnatal Immunisation)
  • Maternal diet the best characterised is the role of low folic acid and Neural Tube Defects (NTDs) see also abnormal neural development and Neural Tube Defects (NTDs). More recently the focus has been on dietary iodine levels and the role they also play on neural development.
  • Maternal drugs effects either prescription drugs (therapeutic chemicals/agents, thalidomide limb development), non-prescription drugs (smoking), and illegal drugs (Cannabis/Marijuana, Methamphetamine/Amphetamine, Cocaine, Heroin, Lysergic Acid Diethylamide)
  • Environment (smoking, chemicals, heavy metals, radiation) and maternal endocrine function (maternal diabetes, thyroid development) and maternal stress.
  • Teratogen synergism, different environmental effects can act individually or in combination on the same developing system. For example, neural development can be impacted upon by alcohol (fetal alcohol syndrome), viral infection (rubella) and/or inadequate dietry folate intake (neural tube defects). These effects may also not be seen as a direct effect on a system or systems but result in a reduced birth weight and the potential postnatal developmental effects. Consider also this in relation to the increasing support to the fetal origins hypothesis.
  • Alcohol - In utero alcohol effects on foetal, neonatal and childhood lung disease.[21]


Links:

Abnormality Links: abnormal development | abnormal genetic | abnormal environmental | Unknown | teratogens | ectopic pregnancy | cardiovascular abnormalities | coelom abnormalities | endocrine abnormalities | gastrointestinal abnormalities | genital abnormalities | head abnormalities | integumentary abnormalities | musculoskeletal abnormalities | limb abnormalities | neural abnormalities | neural crest abnormalities | placenta abnormalities | renal abnormalities | respiratory abnormalities | hearing abnormalities | vision abnormalities | twinning | Developmental Origins of Health and Disease |  ICD-11
Historic Embryology  
1915 Congenital Cardiac Disease | 1917 Frequency of Anomalies in Human Embryos | 1920 Hydatiform Degeneration Tubal Pregnancy | 1921 Anencephalic Embryo | 1921 Rat and Man | 1966 Congenital Malformations
Environmental Links: Introduction | low folic acid | iodine deficiency | Nutrition | Drugs | Australian Drug Categories | USA Drug Categories | thalidomide | herbal drugs | Illegal Drugs | smoking | Fetal Alcohol Syndrome | TORCH | viral infection | bacterial infection | fungal infection | zoonotic infection | toxoplasmosis | Malaria | maternal diabetes | maternal hypertension | maternal hyperthermia | Maternal Inflammation | Maternal Obesity | hypoxia | biological toxins | chemicals | heavy metals | air pollution | radiation | Prenatal Diagnosis | Neonatal Diagnosis | International Classification of Diseases | Fetal Origins Hypothesis
Genetic Links: genetic abnormalities | maternal age | Trisomy 21 | Trisomy 18 | Trisomy 13 | Trisomy X | trisomy mosaicism | Monosomy | Fragile X | Williams | Alagille | Philadelphia chromosome | mitochondria | VACTERL | hydatidiform mole | epigenetics | Prenatal Diagnosis | Neonatal Diagnosis | meiosis | mitosis | International Classification of Diseases | genetics

Critical Periods of Development

Human critical periods of development
  • Finally, when studying this topic remember the concept of critical periods of development that will affect the overall impact of the above listed factors. This can be extended to the potential differences between prenatal and postnatal effects, for example with infections and outcomes.


Critical Periods of Human Development
Conceptus Embryonic development (weeks) Fetal period (weeks)
1
2
3
4
5
6
7
8
9
16
20-36
38
Early zygote.jpg Week2 001 icon.jpg Stage9 sem4c.jpg Stage13 sem1c.jpg Stage15 bf1c.jpg Stage17 bf1c.jpg Stage19 bf1c.jpg Stage23 bf1c.jpg
Neural
Stage2.jpg Heart
Upper limbs
Lower limbs
Ear
Eye
CSt3.jpg Palate
Teeth
Week2 001 icon.jpg External genitalia
Loss Major abnormalities Functional and Minor abnormalities
  Critical Period Links: critical period | abnormal development | Critical Periods table | Image - Critical Periods table | Genital | Opioids | Neural | Thalidomide | Environmental


Self-Directed Learning 6

Links: Embryonic Development | Timeline human development | Movie - Human Development annotated cartoon | Human - critical periods


Australian Drug Categories

Legal drugs are classified, usually by each country's appropriate regulatory body, on the safety of drugs during pregnancy. In Australia, the Therapeutic Goods Authority has classes (A, B1, B2, B3, C, D and X) to define their safety. (More? Australian Drug Categories) In the USA, since 2015 drugs are classified by the Food and Drug Administration (FDA) into new classes to define their safety. The Australian categorisation of medicines for use in pregnancy does not follow a hierarchical structure.

  • Human data are lacking or inadequate for drugs in the B1, B2 and B3 categories
  • Subcategorisation of the B category is based on animal data
  • The allocation of a B category does not imply greater safety than a C category
  • Medicines in category D are not absolutely contraindicated during pregnancy (e.g.anticonvulsants)


  • Pregnancy Category A - Have been taken by a large number of pregnant women and women of childbearing age without an increase in the frequency of malformations or other direct or indirect harmful effects on the fetus having been observed.
  • Pregnancy Category B1 - Drugs which have been taken by only a limited number of pregnant women and women of childbearing age, without an increase in the frequency of malformation or other direct or indirect harmful effects on the human fetus having been observed. Studies in animals have not shown evidence of an increased occurrence of fetal damage.
  • Pregnancy Category B2 - Have been taken by only a limited number of pregnant women and women of childbearing age, without an increase in the frequency of malformation or other direct or indirect harmful effects on the human fetus having been observed. Studies in animals are inadequate or may be lacking, but available data show no evidence of an increased occurrence of fetal damage.
  • Pregnancy Category B3 - Have been taken by only a limited number of pregnant women and women of childbearing age, without an increase in the frequency of malformation or other direct or indirect harmful effects on the human fetus having been observed. Studies in animals have shown evidence of an increased occurrence of fetal damage, the significance of which is considered uncertain in humans.
  • Pregnancy Category C - Have caused or may be suspected of causing, harmful effects on the human fetus or neonate without causing malformations. These effects may be reversible.
  • Pregnancy Category D - Have caused, are suspected to have caused or may be expected to cause, an increased incidence of human fetal malformations or irreversible damage. These drugs may also have adverse pharmacological effects.
  • Pregnancy Category X - Have such a high risk of causing permanent damage to the fetus that they should NOT be used in pregnancy or when there is a possibility of pregnancy.


US FDA - 2015 Pregnancy and Lactation Labeling (Drugs) 2015  
FDA drug category changes 2015.jpg
Since 2015 the labelling classes (A, B, C, D, and X) have been replaced with the new "FDA Pregnancy and Lactation Labeling Rule" (PLLR).
Links: USA Drug Categories | Pregnancy and Lactation Labeling (Drugs) Final Rule

Infant Drug Clearance

Drug clearance rates

The drug clearance data below are only approximate calculated rates for the fetus and infant from NZ Drug Safety in Lactation

Post-conceptual Age (weeks) Clearance of Drug (percentage of adults)
24-28 5%
28-34 10%
34-40 33%
40-44 50%
44-68 66%
> 68 100%


Links: Abnormal Development - Drugs | Australian Fetal Risk Categories | USA FDA Fetal Risk Categories | Therapeutic Goods Authority | Australian Drug Evaluation Committee (ADEC) | TGA - Medicines Pregnancy Database | Appendix A: Therapeutic goods exempted from pregnancy classification | NSW Poisons Information Centre


Self-Directed Learning 7

References

  1. Australian Institute of Health and Welfare 2018. Australia’s mothers and babies 2016—in brief. Perinatal statistics series no. 34. Cat. no. PER 97. Canberra: AIHW.
  2. Australian Institute of Health and Welfare 2017. Australia’s mothers and babies 2015—in brief. Perinatal statistics series no. 33. Cat no. PER 91. Canberra: AIHW.
  3. AIHW 2016. Australia's mothers and babies 2014—in brief. Perinatal statistics series no. 32. [ http://www.aihw.gov.au/publication-detail/?id=60129557656 Cat. no. PER 87]. Canberra: AIHW.
  4. AIHW 2015. Australia's mothers and babies 2013 - in brief. Perinatal statistics series no. 31. Cat. no. PER 72. Canberra: AIHW. PDF Viewed 13 December 2015. http://www.aihw.gov.au/publication-detail/?id=60129553770
  5. Hilder L, Zhichao Z, Parker M, Jahan S, Chambers GM 2014. Australia’s mothers and babies 2012. Perinatal statistics series no. 30. Cat. no. PER 69. Canberra: AIHW. Viewed 16 December 2014. http://www.aihw.gov.au/publication-detail/?id=60129550033
  6. Li Z, Zeki R, Hilder L & Sullivan EA 2013. Australia’s mothers and babies 2011. Perinatal statistics series no. 28. Cat. no. PER 59. Canberra: AIHW.
  7. Li Z, McNally L, Hilder L & Sullivan EA 2011. Australia's mothers and babies 2009 AIHW Perinatal statistics series no. 25 Cat. no. PER 52. Sydney: AIHW National Perinatal Epidemiology and Statistics Unit.
  8. Laws P & Sullivan EA 2010 Australia's mothers and babies 2008 AIHW Perinatal statistics series no. 24 Cat. no. PER 48. Sydney: AIHW National Perinatal Statistics Unit.
  9. Laws P & Sullivan EA 2009. Australia's mothers and babies 2007 AIHW Perinatal statistics series no. 23 Cat. no. PER 48. Sydney: AIHW National Perinatal Statistics Unit.
  10. AIHW National Perinatal Epidemiology and Statistics Unit and AIHW 2013. National core maternity indicators. Cat. no. PER 58. Canberra: AIHW.
  11. Ahrens KA, Thoma M, Copen C, Frederiksen B, Decker E & Moskosky S. (2018). Unintended pregnancy and interpregnancy interval by maternal age, National Survey of Family Growth. Contraception , , . PMID: 29501647 DOI.
  12. Fleming N, Ng N, Osborne C, Biederman S, Yasseen AS, Dy J, Rennicks White R & Walker M. (2013). Adolescent pregnancy outcomes in the province of Ontario: a cohort study. J Obstet Gynaecol Can , 35, 234-245. PMID: 23470111 DOI.
  13. Fitzgerald O, Harris K, Paul RC, Chambers GM. (2017) Assisted reproductive technology in Australia and New Zealand 2015. Sydney: National Perinatal Epidemiology and Statistics Unit, the University of New South Wales Sydney.
  14. Macaldowie A, Wang YA, Chughtai AA & Chambers GM 2014. Assisted reproductive technology in Australia and New Zealand 2012. Sydney: National Perinatal Epidemiology and Statistics Unit, the University of New South Wales. PDF
  15. Confidential Enquiry into Maternal Deaths (CEMD) Why Mothers Die 2000–2002 PDFPDF2
  16. Algert CS, Morris JM, Bowen JR, Giles W & Roberts CL. (2009). Twin deliveries and place of birth in NSW 2001-2005. Aust N Z J Obstet Gynaecol , 49, 461-6. PMID: 19780726 DOI.
  17. Hall JG. (2003). Twinning. Lancet , 362, 735-43. PMID: 12957099 DOI.
  18. Taneja PA, Prosen TL, de Feo E, Kruglyak KM, Halks-Miller M, Curnow KJ & Bhatt S. (2017). Fetal aneuploidy screening with cell-free DNA in late gestation. J. Matern. Fetal. Neonatal. Med. , 30, 338-342. PMID: 27124739 DOI.
  19. Abeywardana S & Sullivan EA 2008. Congenital anomalies in Australia 2002–2003. Birth anomalies series no. 3 Cat. no. PER 41. Sydney: AIHW National Perinatal Statistics Unit.
  20. Centre for Epidemiology and Evidence. New South Wales Mothers and Babies 2015. Sydney: NSW Ministry of Health, 2016.
  21. Gauthier TW & Brown LA. (2017). In utero alcohol effects on foetal, neonatal and childhood lung disease. Paediatr Respir Rev , 21, 34-37. PMID: 27613232 DOI.

Links

The following are links to relevant notes pages that cover the key embryology concepts in this tutorial. These pages and their links will provide further detailed information.

Applied Embryology

Timeline human development | Fetal Development | Birth | Apgar test | Neonatal Development | Week 2 Abnormalities - Trophoblastic Disease | Placenta Development | Neural Abnormalities | Abnormal Development - Folic Acid and Neural Tube Defects | Week 3 | Cardiovascular Abnormalities | Twinning | Blastocyst | Molecular Development

Teratology Links

Human Abnormal Development | Genetic Abnormalities | Environmental Factors | Drugs | Trisomy 21 (Down Syndrome) | Fetal Alcohol Syndrome | Viral Infection | Rubella Virus | Hyperthermia

Self-Directed Learning

Self-Directed Learning 1 - Australian Statistics
Once you have thought about the Australian statistics, now look at the latest report summary Australia’s mothers and babies 2012 and Australian Statistics.
  • What are the current trends in Australia?
  • What factors may be contributing to these changes?
  • Are there any long-term trends in birth statistics?
  • What does this mean for future health care provision?


Self-Directed Learning 2 - Pregnancy
  • What indications would prompt a woman to take a pregnancy test?
  • What test are available and where is test information provided?
  • How much do these tests cost?
  • When does a doctor become involved and what issues should be discussed?


Self-Directed Learning 3 - Assisted Reproductive Technologies
  • Why is this more than "in vitro fertilization"?
  • How many different Assisted Reproductive Technologies are available in Australia?
  • How has the change from DET to SET impacted on reproductive outcomes?
  • What other clinical issues should be considered when discussing ART?
  • What preimplantation genetic tests are currently available?


Self-Directed Learning 4 - The First Few Weeks
  • After fertilization, when does initial implantation occur?
  • Which hormone maintains the initial pregnacy, where is it from and how does it act?
  • How would an ectopic pregnancy differ at this stage?
  • What additional maternal issues should be considered for multiple pregnancies?


Self-Directed Learning 5 - Abnormal Development
  • What are the 3 major forms of abnormal development?
  • What are the main chromosomal abnormalities and how do they occur?
  • How are congenital abnormalities reported and classified within Australia?


Self-Directed Learning 6 - Prenatal Diagnosis
  • What maternal lifestyle issues should be considered for a pregnancy?
  • What diagnostic techniques are currently available and in development?
  • What can ultrasound normally identify?


Self-Directed Learning 7 - Medications in Pregnancy
  • How does drug classification differ between countries?
  • Do european and asian countries apply the same drug classification system(s)?
  • How are teratogens identified?
  • Why does fetal drug clearance differ from maternal clearance?

External Links

External Links Notice - The dynamic nature of the internet may mean that some of these listed links may no longer function. If the link no longer works search the web with the link text or name. Links to any external commercial sites are provided for information purposes only and should never be considered an endorsement. UNSW Embryology is provided as an educational resource with no clinical information or commercial affiliation.

Glossary Links

Glossary: A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | Numbers | Symbols | Term Link



Cite this page: Hill, M.A. (2024, March 28) Embryology BGD Tutorial - Applied Embryology and Teratology. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/BGD_Tutorial_-_Applied_Embryology_and_Teratology

What Links Here?
© Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G