Psych Vivas · Consultation-liaison psychiatry
Perinatal psychiatry in the general hospital — structured clinical viva
Fellowship viva covering hospital perinatal CL: PPP vs blues/OCD, EPDS limits, Patorno lithium, Bergink treatment, sertraline lactation framing, MBU disposition, capacity.
On this page & tools
Target exams
Interpretation
Reveal interpretation
Open with dual-risk emergency framing. Day-4 rapid elevation, sleeplessness, and persecutory ideas about the infant are postpartum psychosis, not blues. Same-day senior review, medical exclusion, secure care, infant safety plan.[1][8]
EPDS. Screening tool for depressive symptoms — does not diagnose or exclude psychosis; full MSE required.[2]
Lithium history. Stopping lithium at conception removed prophylaxis in high-risk bipolar; counsel future pregnancies with Patorno absolute-risk framing and peri-delivery logistics.[3][8]
Treatment. Bergink-style pathway: sleep, antipsychotics, lithium, consider ECT if life-threatening/refractory.[4][7]
Lactation. Individualise; for depression needing SSRI, sertraline often preferred for lactation exposure data — here illness is psychotic/bipolar so prioritise maternal stabilisation and neonatology advice on feeding with chosen agents.[5][4]
Disposition. MBU if available; else psychiatric unit with supervised infant contact.[6]
Core questions and model points
Reveal viva map
- Define hospital perinatal CL — maternity/medical ward liaison across pregnancy and postnatal year; dual mother-infant risk.[1][8]
- Blues vs PPP — days 3–5 mild lability vs rapid psychosis/mania early puerperium.[1]
- EPDS one-liner — depression screen, not full risk tool.[2]
- Patorno one-liner — lithium cardiac malformation risk increased, absolute increase small; counsel and plan.[3]
- PPP acute ladder — medical exclusion, secure setting, sleep, antipsychotic/lithium, ECT threshold.[4][7]
- Sertraline lactation — often preferred SSRI when antidepressant indicated and breastfeeding desired.[5]
- MBU — joint mother-infant psychiatric admission model when available.[6]
- Capacity — decision-specific for discharge with infant and treatment; local law only.[1]
References
- [1]Bergink V, Rasgon N, Wisner KL Postpartum Psychosis: Madness, Mania, and Melancholia in Motherhood Am J Psychiatry, 2016.PMID 27609245
- [2]Cox JL, Holden JM, Sagovsky R Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale Br J Psychiatry, 1987.PMID 3651732
- [3]Patorno E, Huybrechts KF, Hernandez-Diaz S Lithium Use in Pregnancy and the Risk of Cardiac Malformations N Engl J Med, 2017.PMID 28854098
- [4]Bergink V, Burgerhout KM, Koorengevel KM, Kamperman AM, Hoogendijk WJ, Lambregtse-van den Berg MP, et al. Treatment of psychosis and mania in the postpartum period Am J Psychiatry, 2015.PMID 25640930
- [5]Weissman AM, Levy BT, Hartz AJ, Bentler S, Donohue M, Ellingrod VL, et al. Pooled analysis of antidepressant levels in lactating mothers, breast milk, and nursing infants Am J Psychiatry, 2004.PMID 15169695
- [6]Galbally M, Sved-Williams A, Kristianopulos D, Mercuri K, Brown P, Buist A Comparison of public mother-baby psychiatric units in Australia: similarities, strengths and recommendations Australas Psychiatry, 2019.PMID 30407072
- [7]UK ECT Review Group Efficacy and safety of electroconvulsive therapy in depressive disorders: a systematic review and meta-analysis Lancet, 2003.PMID 12642045
- [8]Jones I, Chandra PS, Dazzan P, Howard LM Bipolar disorder, affective psychosis, and schizophrenia in pregnancy and the post-partum period Lancet, 2014.PMID 25455249