Talk:Assisted Reproductive Technology

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Cite this page: Hill, M.A. (2024, April 19) Embryology Assisted Reproductive Technology. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Talk:Assisted_Reproductive_Technology

2012

A novel isolator-based system promotes viability of human embryos during laboratory processing

PLoS One. 2012;7(2):e31010. Epub 2012 Feb 29.

Hyslop L, Prathalingam N, Nowak L, Fenwick J, Harbottle S, Byerley S, Rhodes J, Watson B, Henderson R, Murdoch A, Herbert M. Source Newcastle Fertility Centre, Newcastle upon Tyne, England, United Kingdom.

Abstract

In vitro fertilisation (IVF) and related technologies are arguably the most challenging of all cell culture applications. The starting material is a single cell from which one aims to produce an embryo capable of establishing a pregnancy eventually leading to a live birth. Laboratory processing during IVF treatment requires open manipulations of gametes and embryos, which typically involves exposure to ambient conditions. To reduce the risk of cellular stress, we have developed a totally enclosed system of interlinked isolator-based workstations designed to maintain oocytes and embryos in a physiological environment throughout the IVF process. Comparison of clinical and laboratory data before and after the introduction of the new system revealed that significantly more embryos developed to the blastocyst stage in the enclosed isolator-based system compared with conventional open-fronted laminar flow hoods. Moreover, blastocysts produced in the isolator-based system contained significantly more cells and their development was accelerated. Consistent with this, the introduction of the enclosed system was accompanied by a significant increase in the clinical pregnancy rate and in the proportion of embryos implanting following transfer to the uterus. The data indicate that protection from ambient conditions promotes improved development of human embryos. Importantly, we found that it was entirely feasible to conduct all IVF-related procedures in the isolator-based workstations.

PMID 22393356

Retransplantation of cryopreserved ovarian tissue: the first live birth in Germany

Dtsch Arztebl Int. 2012 Jan;109(1-2):8-13. Epub 2012 Jan 9.

Müller A, Keller K, Wacker J, Dittrich R, Keck G, Montag M, Van der Ven H, Wachter D, Beckmann MW, Distler W. Source Frauenklinik, Universitätsklinikum Erlangen.

Abstract

BACKGROUND: Cryopreserved ovarian tissue can be retransplanted to restore fertility after radiation or chemotherapy. To date, 15 live births after retransplantation have been reported worldwide. We report the first pregnancy and the first live birth after retransplantation in Germany. CASE REPORT: A 25-year-old female patient received initial chemotherapy and radiation of the mediastinum for Hodgkin's lymphoma in 2003 and suffered a relapse two years later. Ovarian tissue was laparoscopically removed and cryopreserved, and she was then treated with high-dose chemotherapy and stem cell transplantation. She remained in remission for 5 years and she could not conceive during this time. The cryopreserved ovarian tissue was thawed and laparoscopically retransplanted into a peritoneal pouch in the ovarian fossa of the right pelvic wall. Three months later, her menopausal symptoms resolved, and she had her first spontaneous menstruation. Six months after retransplantation, after two normal menstrual cycles, low-dose follicle stimulating hormone (FSH) treatment induced the appearance of a dominant follicle in the tissue graft. Ovulation was then induced with human chorionic gonadotropin (HCG), whereupon the patient conceived naturally. After an uncomplicated pregnancy, she bore a healthy child by Caesarean section on 10 October 2011. Histological examination of biopsy specimens revealed that the ovarian tissue of the graft contained follicles in various stages of development, while the original ovaries contained only structures without any reproductive potential. CONCLUSION: This was the first live birth after retransplantation of cryopreserved ovarian tissue in Germany and also the first case with histological confirmation that the oocyte from which the patient conceived could only have come from the retransplanted tissue. In general, young women who will be undergoing chemotherapy and/or radiotherapy for cancer must be informed and counseled about the available options for fertility preservation.

PMID 22282711

Assisted reproductive technology in Europe, 2007: results generated from European registers by ESHRE

Hum Reprod. 2012 Apr;27(4):954-966. Epub 2012 Feb 17.

de Mouzon J, Goossens V, Bhattacharya S, Castilla JA, Ferraretti AP, Korsak V, Kupka M, Nygren KG, Andersen AN; The European IVF-Monitoring (EIM); Consortium for the European Society on Human Reproduction and Embryology (ESHRE). Source ESHRE Central Office, Meerstraat 60, B-1852 Grimbergen, Belgium.

Abstract

BACKGROUND This 11th European IVF-monitoring report presents the results of assisted reproductive technology (ART) treatments initiated in Europe during 2007. METHODS From 33 countries, 1029 clinics reported 493 184 treatment cycles: IVF (120 761), ICSI (256 642), frozen embryo replacement (91 145), egg donation (15 731), preimplantation genetic diagnosis/preimplantation genetic screening (4638), in vitro maturation (660) and frozen oocytes replacements (3607). Overall, this represents a 7.6% increase since 2006, mostly related to an increase in all registers. IUI using husband/partner's (IUI-H) and donor (IUI-D) semen was reported from 23 countries: 142 609 IUI-H (+6.2%) and 26 088 IUI-D (+7.2%). RESULTS In 18 countries where all clinics reported, 376 971 ART cycles were performed in a population of 425.6million (886 cycles per million). The clinical pregnancy rates per aspiration and per transfer were 29.1 and 32.8% for IVF, and 28.6 and 33.0% for ICSI. Delivery rate after IUI-H was 10.2% in women aged < 40 years. In IVF/ICSI cycles, 1, 2, 3 and ≥4 embryos were transferred in 21.4, 53.4, 22.7 and 2.5% of cycles, with no decline in the number of embryos per transfer since 2006. The proportion of multiple deliveries (22.3: 21.3% twin and 1.0% triplet), did not decrease compared with 2006 (20.8%) and 2005 (21.8%). In women < 40 years undergoing IUI-H, twin deliveries occurred in 11.7% and triplets in 0.5%. CONCLUSIONS In comparison with previous years, the reported number of ART cycles in Europe increased in 2007; pregnancy rates increased marginally, but the earlier decline in the number of embryos transferred and multiple births did not continue.

PMID 22343707

Results after ART in 2007

Country Cycles IVF + ICSI IVF ICSI FER ART infantsa ART infants per national births (%)
Aspirations Pregnancies per aspiration (%) Deliveries per aspiration (%) Aspirations Pregnancies per aspiration (%) Deliveries per aspiration (%) Thawings FER Pregnancies per thawing (%) Deliveries per thawing (%)
Albania 145 65 40.0 33.8 78 37.2 29.5 64
Austria 5222 306 30.7
Belgium 3852 29.8 22.4 12 357 28.4 20.6 7499 15.3 11.3 4925 4.1
Bosnia 162 28 32.1 14.3 114 19.3 12.3 19
Bulgaria 1282 532 33.8 25.6 675 31.6 25.8 79 15.2 8.9 378
Cyprus 1305 457 39.2 792 40.2 0.0 155 23.9
Czech Republic 4169 23.5 15.9
Denmark 11 035 5819 26.1 21.3 4952 26.0 21.3 2668 16.5 13.5 3156 4.9
Finland 4724 2830 27.3 20.6 1759 27.9 22.4 3475 21.2 16.0 1875 3.2
France 20 211 24.6 19.2 31 635 25.9 20.5 14 710 1.8
Germany 45 182 10 995 29.4 16.0 32 124 28.2 16.1 17 140 18.3 9.9 10 483 1.5
Greece 2189 780 36.8 26.5 1295 32.8 24.2 193 22.8 14.0 764
Hungary 2437 544 27.4 21.5 1787 28.2 22.8 620 23.1 13.2 776
Iceland 215 25.1 21.9 174 28.2 23.0 168 3.7
Ireland 2864 1466 33.9 27.4 974 29.0 26.3 692 22.4 15.5 958
Italy 40 005 7570 22.0 15.2 28 075 22.0 14.3 709 14.7 8.3 6575 1.2
Latvia 179 104 42.3 75 29.3 113 7.1 20
Lithuania
Macedonia 979 491 30.3 24.2 461 29.1 21.0 29 31.0 20.7 287 1.2
Montenegro 278 24 20.8 20.8 246 22.8 20.3 66 0.8
Norway 5599 2685 30.2 26.1 2703 27.3 23.2 2250 19.7 16.0 1509
Poland 4876 220 33.2 28.2 4547 35.4 29.0 2238 20.9 16.0 2164
Portugal 4496 1329 30.6 23.7 2692 27.9 20.4 524 16.4 11.8 1186 1.2
Russia 21 837 12 171 35.2 24.1 9002 33.1 20.4 3084 23.9 14.9 7197
Serbia 1120 648 24.5 17.3 426 34.5 29.8 277
Slovenia 2882 844 33.9 25.7 1932 28.5 23.7 521 18.8 14.2 913 4.6
Spain 34 499 3041 34.6 27 905 33.6 9089 23.1 12 647
Sweden 10 191 5011 32.0 24.7 4500 28.4 22.4 4500 23.2 17.2 3260 3.1
Switzerland 4503 886 28.1 20.9 3235 27.4 20.1 3312 18.7 12.6 1467
The Netherlands 16 163 8399 27.6 20.5 6659 31.8 25.1 4616 2.5
Turkey 785 34 601 5262 0.5
Ukraine 3946 1790 40.3 29.8 2028 37.4 30.9 579 29.2 22.8 1812
United Kingdom 35 922 15944 30.1 26.4 17 615 31.1 27.5 8549 20.9 18.1 13 838 1.8
Allb 264 022 108 390 29.1 21.1 199 950 28.6 20.2 72493 20.1 13.5 96 690 1.5


Number of embryos transferred and deliveries after ART in 2007

Country In vitro Fertilisation + Intracytoplasmic Sperm Injection Frozen Embryo Replacement
Transfers 1 embryo (%) 2 embryos (%) 3 embryos (% ) 4 + embryos (%) Deliveries Twin (%) Triplet (%) Deliveries Twin (%) Triplet (%)
Albania 131 25.2 29.0 44.3 1.5 45 17.8 2.2
Austria 4912 20.3 68.7 9.8 1.2
Belgium 14 876 50.2 39.6 8.4 1.7 3386 11.8 0.3 845 13.1 0.1
Bosnia 123 49.6 13.8 25.2 11.4 18 5.6 0.0
Bulgaria 1126 8.3 35.6 44.2 11.9 310 14.8 1.6 7 14.3 0.0
Cyprus
Czech Republic 2711 662
Denmark 9226 39.6 55.7 4.5 0.1 2298 16.6 0.1 361 14.1 0.0
Finland 4131 57.8 41.9 0.3 0.0 977 11.3 0.2 560 9.6 0.2
France 44 453 23.2 62.3 13.2 1.3 10 359 18.9 0.4 1913 11.3 0.2
Germany 41 615 12.5 66.9 20.6 0.0 6950 21.2 0.6 1702 15.1 0.6
Greece 1852 11.9 19.3 58.6 10.3 521 25.7 0.8 27 3.7 0.0
Hungary 2146 10.1 45.3 35.7 8.9 524 22.5 2.1 82 18.3 0.0
Iceland 322 46.6 46.0 7.5 0.0 87 17.2 0.0 50 12.0 0.0
Ireland 2221 13.6 77.4 9.0 0.0 658 24.3 0.9 107 17.8 0.0
Italy 30 780 20.4 30.5 49.1 0.0 5158 20.6 2.8 59 6.8 1.7
Latvia 173 15.0 53.8 31.2 0.0
Lithuania
Macedonia 750 23.9 26.9 30.9 18.3 216 26.4 1.4 6 33.3 0.0
Montenegro 258 14.3 32.2 41.1 12.4 55 16.4 1.8
Norway 4821 1324 13.4 0.3 361
Poland 4338 16.6 67.9 15.1 0.4 1382 20.3 0.6 359 12.8 0.0
Portugal 3585 17.4 69.2 13.3 0.2 863 21.6 0.9 62 17.7 0.0
Russia 19 510 16.2 59.6 19.8 4.4 4526 26.0 1.5 460 17.2 1.7
Serbia 911 13.3 77.1 6.9 2.7 239 8.8 3.3
Slovenia 2462 27.6 69.7 2.6 0.0 674 23.0 0.0 74 6.8 0.0
Spain 27 155 5990 27.1 0.7 1092 17.3 0.4
Sweden 8529 69.9 30.1 0.0 0.0 2246 4.6 0.1 776 6.7 0.1
Switzerland 3731 12.8 65.3 21.9 0.0 830 18.9 0.5 417 12.0 0.7
The Netherlands 13 375 3396 15.1 0.1 629 11.0 0.0
Turkey 31 808 11.5 24.1 52.8 11.7 3727 32.9 4.1
Ukraine 3510 11.3 44.2 33.1 11.4 1160 25.0 1.6 132 22.7 0.0
United Kingdom 31 114 12.8 82.3 4.9 0.0 9094 24.1 0.3 1548 17.6 0.3
All* 263 681 21.4 53.4 22.7 2.5 63617 21.3 1.0 11212 13.1 0.3

2011

Sperm storage for cancer patients in the UK: a review of current practice

Hum Reprod. 2011 Nov;26(11):2935-43. Epub 2011 Aug 26.

Sharma V. Source The Leeds Centre for Reproductive Medicine, Seacroft Hospital, Leeds LS146UH, UK. vinay.sharma@leedsth.nhs.uk Abstract An increasing number of cancer patients can now hope to have a full and normal life due to significant improvements in treatment outcomes and survival rates. The application of cryobiology to store fertile gametes before sterilizing treatments has been a natural progression. Greater awareness has markedly increased the worldwide demand for long-term storage of sperm, and has prompted the UK Human Fertilization and Embryology Authority to extend the period of storage permitted by their regulations to 55 years. Other patients undergoing sterilizing chemotherapy and/or radiotherapy such as haemoglobinopathies requiring bone marrow transplantation and autoimmune disorders such as rheumatoid arthritis may further increase the indications for sperm storage. Most adult and adolescent patients and their relatives/spouses/parents/guardians value this service even though very few eventually use the sperm. There is an urgent need to develop national and international guidelines for the provision, organization, maintenance and management of the cryopreservation services.

PMID 21873609

Bivariate analysis of basal serum anti-Müllerian hormone measurements and human blastocyst development after IVF

Reprod Biol Endocrinol. 2011 Dec 2;9:153.

Sills ES, Collins GS, Brady AC, Walsh DJ, Marron KD, Peck AC, Walsh AP, Salem RD. Source Division of Reproductive Endocrinology, Pacific Reproductive Center, Irvine, California, USA. dr.sills@prc-ivf.com

Abstract

BACKGROUND: To report on relationships among baseline serum anti-Müllerian hormone (AMH) measurements, blastocyst development and other selected embryology parameters observed in non-donor oocyte IVF cycles. METHODS: Pre-treatment AMH was measured in patients undergoing IVF (n = 79) and retrospectively correlated to in vitro embryo development noted during culture. RESULTS: Mean (+/- SD) age for study patients in this study group was 36.3 ± 4.0 (range = 28-45) yrs, and mean (+/- SD) terminal serum estradiol during IVF was 5929 +/- 4056 pmol/l. A moderate positive correlation (0.49; 95% CI 0.31 to 0.65) was noted between basal serum AMH and number of MII oocytes retrieved. Similarly, a moderate positive correlation (0.44) was observed between serum AMH and number of early cleavage-stage embryos (95% CI 0.24 to 0.61), suggesting a relationship between serum AMH and embryo development in IVF. Of note, serum AMH levels at baseline were significantly different for patients who did and did not undergo blastocyst transfer (15.6 vs. 10.9 pmol/l; p = 0.029). CONCLUSIONS: While serum AMH has found increasing application as a predictor of ovarian reserve for patients prior to IVF, its roles to estimate in vitro embryo morphology and potential to advance to blastocyst stage have not been extensively investigated. These data suggest that baseline serum AMH determinations can help forecast blastocyst developmental during IVF. Serum AMH measured before treatment may assist patients, clinicians and embryologists as scheduling of embryo transfer is outlined. Additional studies are needed to confirm these correlations and to better define the role of baseline serum AMH level in the prediction of blastocyst formation. PMID 22136508

Historic

In vitro fertilization and cleavage of human ovarian eggs

Am J Obstet Gynecol. 1948 Mar;55(3):440-52.

MENKIN MF, ROCK J.

  • Miriam Menken and John Rock retrieved more than 800 oocytes from women during operations for various conditions.
  • One hundred and thirty-eight of these oocytes were exposed to spermatozoa in vitro.

PMID 18903892


IN VITRO FERTILIZATION AND CLEAVAGE OF HUMAN OVARIAN EGGS

Science. 1944 Aug 4;100(2588):105-7.

Rock J, Menkin MF.


PMID 17788930 http://www.sciencemag.org/content/100/2588/105.long

USA

Assisted Reproductive Technology Surveillance - United States, 2006

Assisted Reproductive Technology Surveillance - United States, 2006

Assisted reproductive technology surveillance--United States, 2006. Sunderam S, Chang J, Flowers L, Kulkarni A, Sentelle G, Jeng G, Macaluso M; Centers for Disease Control and Prevention (CDC). MMWR Surveill Summ. 2009 Jun 12;58(5):1-25. PMID: 19521336 [PubMed - indexed for MEDLINE]Free Article Related citations


Assisted reproductive technology surveillance--United States, 2005. Wright VC, Chang J, Jeng G, Macaluso M; Centers for Disease Control and Prevention (CDC). MMWR Surveill Summ. 2008 Jun 20;57(5):1-23. Erratum in: MMWR Surveill Summ. 2009 Mar 6;58(8):203-4. MMWR Surveill Summ. 2008 Oct 10;57(40):1105. PMID: 18566567 [PubMed - indexed for MEDLINE]Free Article Related citations


Assisted reproductive technology surveillance - United States, 2004. Wright VC, Chang J, Jeng G, Chen M, Macaluso M; Centers for Disease Control and Prevention. MMWR Surveill Summ. 2007 Jun 8;56(6):1-22. Erratum in: MMWR Morb Mortal Wkly Rep. 2007 Jul 6;56(26):658. PMID: 17557073 [PubMed - indexed for MEDLINE]Free Article Related citations


Assisted reproductive technology surveillance--United States, 2000. Wright VC, Schieve LA, Reynolds MA, Jeng G. MMWR Surveill Summ. 2003 Aug 29;52(9):1-16. Erratum in: MMWR 2003 Oct 3; 52(39):942. PMID: 14532867 [PubMed - indexed for MEDLINE]Free Article Related citations


Assisted reproductive technology surveillance--United States, 2003. Wright VC, Chang J, Jeng G, Macaluso M. MMWR Surveill Summ. 2006 May 26;55(4):1-22. PMID: 16723970 [PubMed - indexed for MEDLINE]Free Article Related citations


Assisted reproductive technology surveillance--United States, 2001. Wright VC, Schieve LA, Reynolds MA, Jeng G, Kissin D. MMWR Surveill Summ. 2004 Apr 30;53(1):1-20. PMID: 15123982 [PubMed - indexed for MEDLINE]Free Article Related citations


Assisted reproductive technology surveillance--United States, 2002. Wright VC, Schieve LA, Reynolds MA, Jeng G; Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention (CDC). MMWR Surveill Summ. 2005 Jun 3;54(2):1-24. PMID: 15931153 [PubMed - indexed for MEDLINE]Free Article Related citations


Pregnancy outcomes after assisted reproductive technology. Allen VM, Wilson RD, Cheung A; Genetics Committee of the Society of Obstetricians and Gynaecologists of Canada (SOGC); Reproductive Endocrinology Infertility Committee of the Society of Obstetricians and Gynaecologists of Canada (SOGC). J Obstet Gynaecol Can. 2006 Mar;28(3):220-50. English, French. PMID: 16650361 [PubMed - indexed for MEDLINE] Related citations


Preconception and interconception health status of women who recently gave birth to a live-born infant--Pregnancy Risk Assessment Monitoring System (PRAMS), United States, 26 reporting areas, 2004. D'Angelo D, Williams L, Morrow B, Cox S, Harris N, Harrison L, Posner SF, Hood JR, Zapata L; Centers for Disease Control and Prevention (CDC). MMWR Surveill Summ. 2007 Dec 14;56(10):1-35. Erratum in: MMWR Morb Mortal Wkly Rep. 2008 Apr 25;57(16):436. PMID: 18075488 [PubMed - indexed for MEDLINE]Free Article Related citations


From the Centers of Disease Control and Prevention. Use of assisted reproductive technology--United States, 1996 and 1998. Centers for Disease Control and Prevention (CDC). MMWR Morb Mortal Wkly Rep. 2002 Feb 8;51(5):97-101. PMID: 11892956 [PubMed - indexed for MEDLINE]Free Article Related citations


Single-embryo transfer reduces clinical pregnancy rates and live births in fresh IVF and Intracytoplasmic Sperm Injection (ICSI) cycles: a meta-analysis. Baruffi RL, Mauri AL, Petersen CG, Nicoletti A, Pontes A, Oliveira JB, Franco JG Jr. Reprod Biol Endocrinol. 2009 Apr 23;7:36. PMID: 19389258