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O&G VivasReproductive endocrinology and infertility

O&G Vivas · Reproductive endocrinology and infertility

Assisted reproductive technology — structured oral station (12 minutes)

FRANZCOG oral-format station on assisted reproduction: the candidate frames the ART pathway, justifies the protocol (antagonist with agonist trigger) and embryo-transfer number (elective single), and counsels honestly on age-stratified cumulative live birth and the complications of ART. Scored against the eight published RANZCOG oral domains.

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FRANZCOGMRCOGABOG
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Target exams

FRANZCOGMRCOGABOG
Prompt
A 38-year-old woman and her 40-year-old partner are referred to the fertility clinic after two years of infertility. Her tubes are patent, her ovarian reserve is normal, and his semen analysis shows severe oligoasthenoteratozoospermia. They have asked their general practitioner for IVF. The examiner will ask you to outline the plan from this point — the work-up, the IVF/ICSI pathway, the protocol and embryo-transfer decisions, and the counselling on their realistic chance of success and the risks.

Station format

4 minutes reading, 12 minutes examination, 20 marks, global scoring. The eight published RANZCOG oral domains apply to every station: history and examination; investigations and interpreting results; treatment and management; clinical knowledge; complex, urgent or unusual clinical presentations; rapport with patient, support person or colleague; respect; communication skills. You are being marked on how you behave, not only what you know. [1]

Reveal the examiner script and model responsesShowHide

Opening prompt — "Outline your plan from this point."

Model response — say it in this order: [1][2]

  • "They meet the definition of infertility — failure to conceive after two years — and the indication for ART is severe male factor, which means ICSI rather than conventional IVF, first described by Palermo in 1992."
  • "Before treatment I would complete the work-up — repeat the semen analysis, arrange male hormonal and genetic assessment (karyotype, cystic fibrosis carrier status, Y-microdeletion), confirm her ovarian reserve and uterine cavity, and do infectious-disease screening."
  • "I would walk them through the staged pathway — suppress, stimulate, trigger, retrieve, fertilise by ICSI, culture, transfer with luteal support — and counsel them honestly on age-stratified cumulative success."[2]

Examiner is listening for: the pathway named in order, the ICSI indication justified, and honest age-aware counselling. [1]

Probe 1 — "Which stimulation protocol would you choose, and why?"

  • "A GnRH antagonist protocol, not the long agonist. The Cochrane review shows a substantial reduction in OHSS with the antagonist — OR 0.61 — without lowering live birth, which was comparable (OR 1.02)."[3]
  • "The decisive advantage is that the antagonist protocol permits a GnRH agonist trigger instead of hCG, which is the single most powerful lever against early OHSS. I would individualise her gonadotrophin dose by age, BMI, antral follicle count and prior response."[3]

Probe 2 — "How many embryos would you transfer, and what luteal support?"

  • "Elective single embryo transfer. ASRM and SART refine the number of embryos to transfer specifically to promote singleton gestation and reduce multiple pregnancies — and multiple pregnancy is the single biggest iatrogenic risk of ART."[6]
  • "For luteal support, progesterone, never hCG — the Cochrane review found hCG carries a higher OHSS risk and should be avoided; progesterone is the best option."[5]

Probe 3 — "They are 38 and 40. What is their realistic chance of a live birth?"

  • "I would counsel on cumulative live birth across a full course of treatment, because that is what matters to them. Malizia's data show that at 40 or older, cumulative live birth after up to six cycles was 23% conservative to 42% optimistic, versus 65% to 86% under 35."[4]
  • "The honest message — which the authors state — is that IVF may largely overcome infertility in younger women, but it does not reverse the age-dependent decline. Given her age, I would discuss the option of donor oocytes early rather than late."[4]

Probe 4 — "She asks whether her baby will be healthy. How do you answer?"

This is a scored domain, not a courtesy. Demonstrate it out loud: [1]

  • Answer honestly and proportionately: "ART singletons have slightly higher perinatal risk than naturally conceived singletons — longer birth admissions and a bit more hospital use in early childhood — but these differences are far smaller than the risks of an ART multiple birth, and much of it reflects the subfertility itself, not the technique."[6]
  • "The single biggest thing we can do to protect the pregnancy is to transfer one embryo, so you carry a singleton rather than twins."
  • Offer written information and a follow-up counselling visit; acknowledge the emotional weight without minimising the real, if modest, risks.

Probe 5 — "Name the complications of ART you would warn them about."

  • "OHSS — the iatrogenic emergency of stimulation; we prevent it upstream with the antagonist protocol and agonist trigger, and I would teach them the warning symptoms — abdominal distension, breathlessness, reduced urine output."[3]
  • "Multiple pregnancy — prevented by elective single embryo transfer; and the procedural risks of retrieval — bleeding, infection, ovarian torsion and anaesthetic events."[6]
  • "And the slightly higher perinatal risk of ART singletons, much of it attributable to the underlying subfertility."[6]
Obstetrics & Gynaecology Pro

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You have read the opening of this viva. The complete unit — every section and its primary-source references — is part of the Obstetrics & Gynaecology fellowship library.

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References6ShowHide
  1. [1]Zegers-Hochschild F, Adamson GD, Dyer S, Racowsky C, de Mouzon J, Sokol R, Rienzi L, Sunde A, Schmidt L, Cooke ID, Simpson JL, van der Poel S The International Glossary on Infertility and Fertility Care, 2017 Hum Reprod, 2017.PMID 29117321
  2. [2]Palermo G, Joris H, Devroey P, Van Steirteghem AC Pregnancies after intracytoplasmic injection of single spermatozoon into an oocyte Lancet, 1992.PMID 1351601
  3. [3]Al-Inany HG, Youssef MA, Ayeleke RO, Brown J, Lam WS, Broekmans FJ Gonadotrophin-releasing hormone antagonists for assisted reproductive technology Cochrane Database Syst Rev, 2016.PMID 27126581
  4. [4]Malizia BA, Hacker MR, Penzias AS Cumulative live-birth rates after in vitro fertilization N Engl J Med, 2009.PMID 19144939
  5. [5]van der Linden M, Buckingham K, Farquhar C, Kremer JA, Metwally M Luteal phase support for assisted reproduction cycles Cochrane Database Syst Rev, 2011.PMID 21975790
  6. [6]Practice Committee of the American Society for Reproductive Medicine and the Practice Committee for the Society for Assisted Reproductive Technologies Guidance on the limits to the number of embryos to transfer: a committee opinion Fertil Steril, 2021.PMID 34330423
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