BGDA Practical 12 - Third Trimester

From Embryology
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Practical 12: Embryo to Fetus | Second Trimester | Third Trimester | Birth | Neonatal | Abnormalities


Introduction

Historic drawing of the fetus in the uterus at 8 months compared to non-pregnant uterus size.
  • Survival issues for early delivery
  • Fetal Respiratory
  • Fetal Genital
  • Fetal weight
  • Fetal Neural
  • Fetal Cardiovascular
  • Fetal Renal
  • Fetal Growth - Fetal Growth Restriction, Developmental Origins of Health and Disease

Week 24+

  • Earliest potential survival expected if born.
  • Most of the serious illness and mortality is concentrated in the 1 to 2 percent of infants who are born at less than GA 32 weeks (week 30) and who weigh less than 1500 g.

Class Models

Observe the differences between the fetus and uterus at the end of the second trimester and at term.

  • size and weight

Fetal Weight

Fetal weight change.jpg


Endocrine

During the third trimester fetal endocrine organs are differentiated and secreting fetal hormones.

Fetal thymus weight growth graph

Endocrine - Fetal thymus weight growth

Respiratory

Week 24 to 40 lung histology - terminal sac, end month 6 alveolar cells type 2 appear and begin to secrete surfactant
  • saccule - a large thin-walled airspace lined by flattened epithelium present from about GA 28 weeks to 2 months after birth
Alveolar-sac-01.jpg

Genital

Testis 001 icon.jpg
 ‎‎Testis Descent
Page | Play

Testes Descent

The linked animation shows the descent of the testes (between week 7 to 38, birth).

Descent of the testes into the scrotal sac begins generally during week 26 and may take several days.

  • testis (white) lies in the subserous fascia (spotted)
  • a cavity processus vaginalis evaginates into the scrotum
  • gubernaculum (green) attached to the testis shortens drawing it into the scotal sac
  • as it descends it passes through the inguinal canal extends
    • from the deep ring (transversalis fascia)
    • to the superficial ring (external oblique muscle)

Incomplete or failed descent can occur unilaterally or bilaterally, is more common in premature births, and can be completed postnatally. (see also cryptorchidism).

Testis-descent start.jpg Testis-descent end.jpg
Start of testis descent End of testis descent

Neural

Dev anat 01.jpg Comparison of brain growth through the third trimester.


  • Increasing cortex surface area forming visible gyri (folds) and fissures (grooves) on the surface.
  • Electroencephalogram (EEG) activity first seen in third trimester GA 7 months.


Links: Neural System Development

Neural-development.jpg

Renal

Adult nephron structure
Nephron histology

The functional unit of the kidney is the nephron and the process of their initial formation is called nephrogenesis. During development nephron number increases from about 15,000 at 15 weeks (GA 17 weeks) increasing to about the adult number by 36 weeks. Each adult kidney typically contains about 750,000 nephrons, though the total number can vary significantly from as few as 250,000 to as many as 2,000,000.

Fetal kidney MRI 01.jpg

MRI appearance of normal fetal kidneys.(GA 25)


In humans, nephrogenesis only occurs before birth, though nephron maturation continues postnatally.

Nephron development has four identifiable developmental stages:
  1. Vesicle (V) stage (13-19 weeks, second trimester)
  2. S-shaped body (S) stage ( 20-24 weeks, second trimester)
  3. Capillary loop (C) stage (25-29 weeks, third trimester)
  4. Maturation (M) stage (infants aged 1-6 months, neonatal and postnatal)
Glomerular podocyte cartoon 02.jpg

Infant Drug Clearance

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%
Renal drug clearance data only approximate calculated rates for the fetus and infant. Graph version

Based on: NZ Drug Safety in Lactation

Drug clearance rates


Teratogen (Greek, teraton = monster) Any agent that causes a structural abnormality following exposure during pregnancy. The overall effect depends on dosage and time of exposure.

Fetal Growth

Fetal Growth Restriction

The term "Fetal Growth Restriction" (FGR) or intrauterine growth restriction (IUGR) are used to describe when the fetus does not reach full growth potential. This is usually determined by clinical sonography calculations of fetal weight, fetal size, or symmetry.

Developmental Origins of Health and Disease (DOHaD)

Environmental derived abnormalities relate to maternal lifestyle, environment and nutrition and while some of these directly effect embryonic development, there is also growing evidence that some effects are more subtle and relate to later life health events. This theory, now called "developmental origins of health and disease" (DOHAD or DOHaD) and also previously Fetal Origins Hypothesis, is based on the early statistical analysis carried out by David Barker (1938 - 2013) of low birth weight data collected in the early 1900's in the south east of England which he then compared with these same babies later health outcomes. The theory was therefore originally called the "Barker Hypothesis" and has recently been renamed as "fetal origins" or "programming". Several origins have been suggested including: fetal undernutrition, endocrine (increased cortisol exposure), genetic susceptibility and accelerated postnatal growth.



Links: Developmental Origins of Health and Disease


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Practical 12: Embryo to Fetus | Second Trimester | Third Trimester | Birth | Neonatal | Abnormalities


   


Additional Information

Additional Information - Content shown under this heading is not part of the material covered in this class. It is provided for those students who would like to know about some concepts or current research in topics related to the current class page.
Links: Third Trimester

Abnormal Neural

Quantitative Folding Pattern Analysis of Early Primary Sulci in Human Fetuses with Brain Abnormalities[1]

"Aberrant gyral folding is a key feature in the diagnosis of many cerebral malformations. However, in fetal life, it is particularly challenging to confidently diagnose aberrant folding because of the rapid spatiotemporal changes of gyral development. Currently, there is no resource to measure how an individual fetal brain compares with normal spatiotemporal variations. In this study, we assessed the potential for automatic analysis of early sulcal patterns to detect individual fetal brains with cerebral abnormalities. ... Automated analysis of interrelated patterning of early primary sulci could outperform the traditional gyrification index and has the potential to quantitatively detect individual fetuses with emerging abnormal sulcal patterns."
  • Gyrification index - a metric that quantifies the amount of cortex buried within the sulcal folds as compared with the amount of cortex on the outer visible cortex.[2] (More? Watch the JoVE Video)

Third Trimester

(Clinical Week 28) Third Trimester


Week
Stage
Event
Clinical third trimester Fetal size change.jpg Hearing 3rd Trimester - vibration acoustically of maternal abdominal wall induces startle respone in fetus.
27
 
28
  Respire Month 7 - respiratory bronchioles proliferate and end in alveolar ducts and sacs
29
 
30
   

Genital male gonad (testes) descending

31
 
32
  Nail Development fingernails reach digit tip
33
  Neural brain cortical sulcation - primary sulci present[3]
34
  Neural brain cortical sulcation - insular, cingular, and occipital secondary sulci present[3]
35
   
36
  Frazer006 bw600.jpg Nail Development toenails reach digit tip

Lens Development - lens growth and interocular distance plateaus after 36 weeks of gestation[4]

37
   
38
Birth Newborn.jpg Clinical Week 40

Heart pressure difference closes foramen ovale leaving a fossa ovalis

Thyroid TSH levels increase, thyroxine (T3) and T4 levels increase to 24 h, then 5-7 days postnatal decline to normal levels

Adrenal - zona glomerulosa, zona fasiculata present



References

  1. K Im, A Guimaraes, Y Kim, E Cottrill, B Gagoski, C Rollins, C Ortinau, E Yang, P E Grant Quantitative Folding Pattern Analysis of Early Primary Sulci in Human Fetuses with Brain Abnormalities. AJNR Am J Neuroradiol: 2017; PubMed 28522661
  2. Marie Schaer, Meritxell Bach Cuadra, Nick Schmansky, Bruce Fischl, Jean-Philippe Thiran, Stephan Eliez How to measure cortical folding from MR images: a step-by-step tutorial to compute local gyrification index. J Vis Exp: 2012, (59);e3417 PubMed 22230945
  3. 3.0 3.1 C Garel, E Chantrel, H Brisse, M Elmaleh, D Luton, J F Oury, G Sebag, M Hassan Fetal cerebral cortex: normal gestational landmarks identified using prenatal MR imaging. AJNR Am J Neuroradiol: 2001, 22(1);184-9 PubMed 11158907
  4. L B Paquette, H A Jackson, C J Tavaré, D A Miller, A Panigrahy In utero eye development documented by fetal MR imaging. AJNR Am J Neuroradiol: 2009, 30(9);1787-91 PubMed 19541779


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Cite this page: Hill, M.A. 2017 Embryology BGDA Practical 12 - Third Trimester. Retrieved September 22, 2017, from https://embryology.med.unsw.edu.au/embryology/index.php/BGDA_Practical_12_-_Third_Trimester

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© Dr Mark Hill 2017, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G