Evidence map›Paper›PMID 39031964›Full record

ArticleSchizophrenia bulletin2026

Clozapine Safety in Pregnancy: A Clinical Study.

Jayashri Kulkarni, Adam De Chellis, Heather Gilbert, Emmy Gavrilidis, Eveline Mu, Leila Karimi, Qi Li

Abstract read
In one paragraph

Article in Schizophrenia bulletin, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Jayashri KulkarniHER Centre Australia, Department of Psychiatry, School of Translational Medicine, Monash University, Melbourne, Australia.
Adam De ChellisHER Centre Australia, Department of Psychiatry, School of Translational Medicine, Monash University, Melbourne, Australia.
Heather GilbertHER Centre Australia, Department of Psychiatry, School of Translational Medicine, Monash University, Melbourne, Australia.
Emmy GavrilidisHER Centre Australia, Department of Psychiatry, School of Translational Medicine, Monash University, Melbourne, Australia.
Eveline MuHER Centre Australia, Department of Psychiatry, School of Translational Medicine, Monash University, Melbourne, Australia.
Leila KarimiHER Centre Australia, Department of Psychiatry, School of Translational Medicine, Monash University, Melbourne, Australia.
Qi LiHER Centre Australia, Department of Psychiatry, School of Translational Medicine, Monash University, Melbourne, Australia.

Funding

Australian Rotary Health Research FundEli-Lilly & Company
6 · The paper itself

Abstract

background and hypothesisPregnant women with persistent schizophrenia and related disorders may require ongoing antipsychotic treatment, including clozapine. However, the potential risks of using clozapine during pregnancy and the postnatal period remain uncertain. STUDY

designWe conducted a nested case-control study using the National Register of Antipsychotic Medication in Pregnancy (NRAMP) database. Our study assessed pregnancy outcomes among Australian women diagnosed with schizophrenia spectrum disorder and treated with clozapine (n = 14) during the first trimester. These women were compared to 2 subgroups: those treated with quetiapine (n = 53) and those not taking any medication (n = 24) during pregnancy. STUDY

resultsWe observed higher rates of miscarriage in the clozapine group compared to the quetiapine and drug-free groups. The clozapine group had a higher early pregnancy body mass index but lower overall pregnancy weight gain than the other groups. The prevalence of gestational diabetes was significantly higher in the clozapine group. The percentage of vaginal delivery was higher in the clozapine group than in the other 2 groups. Neonatal outcomes such as gestational age, and Apgar scores were similar across groups. The birth weight was lower in the clozapine group compared to the other 2 groups.

conclusionsThis study suggests that pregnant women taking clozapine and their babies have greater adverse outcomes compared to other groups. Clozapine appears to be associated with a greater risk of miscarriages, maternal gestational diabetes, and lower birth weight. However, the gestational age, Apgar scores, and admission to NICU/SCN were comparable between all groups.

Indexed as

Abortion, SpontaneousAntipsychotic AgentsClozapineDiabetes, GestationalPregnancy ComplicationsPregnancy OutcomeQuetiapine FumarateRegistriesSchizophreniaAdultAustraliaCase-Control StudiesFemaleHumansInfant, NewbornPregnancyAntipsychotic AgentsClozapineQuetiapine Fumarateantipsychotic medicationclozapinegestational diabetespostnatalprenatalquetiapine

Identifiers

PMID39031964
PMCPMC12996916

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.