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O&G SAQsAntenatal care — maternal age and ART

O&G SAQs · Antenatal care — maternal age and ART

Advanced maternal age and ART singleton — structured SAQ (15 marks)

FRANZCOG-format structured SAQ on advanced maternal age and ART-conceived singleton pregnancy: distinguishing age, subfertility and ART risk contributions; risk-tailored surveillance for preeclampsia and growth; counselling on congenital anomalies and imprinting disorders (Davies NEJM, Lazaraviciute meta-analysis); and the timing-of-birth conversation anchored on the Reddy stillbirth data. Per-sub-part marking rubric included.

15 marks20 min3 min readVerification in progress

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FRANZCOGMRCOGABOG
Prompt
You are the obstetric registrar in the antenatal clinic. A 41-year-old G1P0 woman at 11 weeks' gestation is booked after conceiving by ICSI following seven years of primary infertility. Her booking BMI is 31, blood pressure 128/80, and she has no past medical history of note. (a) Identify the three independent risk contributions to her pregnancy and briefly explain how each contributes to her risk profile. (3 marks) (b) Outline her surveillance plan for preeclampsia and fetal growth, citing the relevant evidence. (5 marks) (c) She asks whether her ICSI-conceived baby is at higher risk of congenital anomalies and imprinting disorders. Counsel her using the relevant evidence. (4 marks) (d) At 39 weeks' gestation with a normal antenatal course, she asks about timing and mode of birth. Outline your counselling, including the stillbirth data that informs the discussion. (3 marks)

How this SAQ is marked

Twelve SAQs, 180 marks, two 2-hour papers — roughly 15 marks and 20 minutes each. Marks come from specifics and discrimination: the named risk contribution, the evidence quoted by author and number, the surveillance plan with the doppler and aspirin specifics. Write in short labelled points, not prose paragraphs. Answer the sub-part you are asked.[1][5]

Reveal model answer and mark schemeShowHide

(a) Three independent risk contributions (3 marks)

One mark per contribution with a brief explanation. [5][6]

  • Age (41 years — very advanced maternal age) — higher aneuploidy, gestational diabetes, preeclampsia, stillbirth and caesarean; the risks rise exponentially from the mid-thirties.
  • Subfertility (seven years primary infertility) — subfertility itself is an independent risk factor for adverse outcomes, including preeclampsia, preterm birth and perinatal mortality, independent of ART.[5]
  • ART (ICSI conception) — IVF/ICSI singleton pregnancies carry excess risk of preterm birth, low birthweight, small-for-gestational-age, hypertensive disorders and perinatal mortality compared with spontaneous conceptions (Pandey 2012).[3]
  • Plus BMI 31 (a fourth, bonus factor) — a moderate preeclampsia risk factor in its own right.

(b) Surveillance plan for preeclampsia and fetal growth (5 marks)

One mark per element, maximum five. [3][7]

  • Low-dose aspirin from 12 weeks to 36 weeks — she has multiple preeclampsia risk factors (nulliparity, age 35 or older, ART-conceived pregnancy, BMI over 30), so low-dose aspirin is clearly indicated, dosed per local guideline.[7]
  • Uterine artery Doppler in mid-gestation — to stratify risk; normal Dopplers reduce the predicted preeclampsia risk.
  • Serial growth scans through the third trimester — the ART singleton excess risk of small-for-gestational-age and preterm birth warrants this; umbilical artery Doppler if growth-restricted.[3]
  • Gestational diabetes screening — early glycaemic assessment given her age and BMI, with formal testing in mid-pregnancy.
  • Blood pressure monitoring at every visit with a low threshold for investigation of symptoms and heightened surveillance for the older mother.

(c) Counselling on congenital anomalies and imprinting disorders (4 marks)

One mark per point, maximum four. [2][4]

  • Congenital anomalies are modestly increased in ART singletons. The Davies 2012 NEJM study found an adjusted odds ratio of 1.28 for any birth defect with assisted conception overall; the ICSI signal persisted after adjustment (adjusted OR 1.57), although residual confounding cannot be excluded. A history of infertility was also associated.[2]
  • Imprinting disorders are increased but the absolute risk is small. The Lazaraviciute 2014 meta-analysis found a combined odds ratio of 3.67 (95% CI 1.39 to 9.74) for any imprinting disorder in IVF/ICSI children compared with spontaneous conception.[4]
  • The clinically recognised syndromes are Beckwith-Wiedemann (macrosomia, lateralised overgrowth, abdominal wall defects, neonatal hypoglycaemia) and Angelman syndrome (severe developmental delay, seizures, ataxia), with weaker signals for Russell-Silver.
  • Counselling principle: a small absolute increase on a rare baseline. Do not overstate; do not ignore. The large majority of ICSI children are healthy.

(d) Timing and mode of birth at 39 weeks (3 marks)

One mark per element, maximum three. [1]

  • Quote the Reddy 2006 stillbirth data: at 37 to 41 weeks, the risk of stillbirth is about 1 in 382 ongoing pregnancies for ages 35 to 39 and about 1 in 267 for age 40 or older — roughly 99.6% of ongoing term pregnancies in women over 40 end in a live birth.[1]
  • There is no evidence for routine early induction in advanced maternal age alone — the decision to offer induction at 39 to 40 weeks is shared, weighing the stillbirth risk against the iatrogenic prematurity and caesarean risks of induction.
  • Mode of birth is for obstetric indications — caesarean is not mandated by age or ART alone; offer a vaginal birth with a clear plan for monitoring and escalation. Counsel honestly about the higher caesarean rate in older ART mothers and the reasons for it.
Obstetrics & Gynaecology Pro

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

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References7ShowHide
  1. [1]Reddy UM, Ko CW, Willinger M Maternal age and the risk of stillbirth throughout pregnancy in the United States Am J Obstet Gynecol, 2006.PMID 16949411
  2. [2]Davies MJ, Moore VM, Willson KJ, et al. Reproductive technologies and the risk of birth defects N Engl J Med, 2012.PMID 22559061
  3. [3]Pandey S, Shetty A, Hamilton M, et al. Obstetric and perinatal outcomes in singleton pregnancies resulting from IVF/ICSI: a systematic review and meta-analysis Hum Reprod Update, 2012.PMID 22611174
  4. [4]Lazaraviciute G, Kauser M, Bhattacharya S, et al. A systematic review and meta-analysis of DNA methylation levels and imprinting disorders in children conceived by IVF/ICSI compared with children conceived spontaneously Hum Reprod Update, 2014.PMID 24961233
  5. [5]Luke B Pregnancy and birth outcomes in couples with infertility with and without assisted reproductive technology: with an emphasis on US population-based studies Am J Obstet Gynecol, 2017.PMID 28322775
  6. [6]Luke B, Brown MB, Wantman E, et al. Risk of severe maternal morbidity by maternal fertility status: a US study in 8 states Am J Obstet Gynecol, 2019.PMID 30321527
  7. [7]Zhang H, Wang W Risk factors and adverse pregnancy outcomes in older pregnant women with hypertensive disorders of pregnancy J Obstet Gynaecol Res, 2022.PMID 35596590
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