Study | Country Study period |
Population source | Exposure definition | Non-exposure definition | Sample size | Rmk |
---|---|---|---|---|---|---|
Bruno, 2024 |
Denmark, Finland, Iceland, Norway, and Sweden 2000 - 2020 |
Pregnant women with a diagnosis of a psychiatric condition (ICD-10 codes: F10– F49, F60–F98, X60–X84, and Y10–Y34) in the 12 months before pregnancy start. | Pregnant women who filled ≥1 prescription for Quetiapine monotherapy (among antipsychotic medication) anytime between pregnancy start (based on the date of the first day of the last menstrual period) until the date of birth. |
unexposed, sick
Pregnant women who did not fill a prescription for any antipsychotic from 90 days before the start of pregnancy until birth. |
4492 / 197296 | Authors assessed several atypical antipsychotics (adjusted results), thus to avoid redundancy of controls, only one substance was reported in class meta-analysis (this one with the higher number of pregnancies). |
Chan (Controls exposed to FGA), 2024 |
China 2003 - 2018 |
All pregnant women aged 15–50 years who gave a singleton live birth or stillbirth (≥20 weeks of gestation) in public hospitals in Hong Kong between January 1, 2003, and December 31, 2018. | Pregnant women filling at least one prescription of quetiapine only (without other antipsychotic) during the first trimester of pregnancy, which is defined as the first 90 days after the last menstrual period (LMP). |
exposed to other treatment, sick
Pregnant women filling at least one prescription of any first generation antipsychotic (only, i.e no second generation antipsychotic) during the first trimester of pregnancy, which is defined as the first 90 days after the last menstrual period (LMP). |
191 / 420 | Pregnancies with gestational age < 20 weeks, chromosomal abnormalities, fetal alcohol syndrome, abnormalities due to maternal infection, or exposure to known teratogens were excluded. |
Chan (Controls unexposed, general pop), 2024 |
China 2003 - 2018 |
All pregnant women aged 15–50 years who gave a singleton live birth or stillbirth (≥20 weeks of gestation) in public hospitals in Hong Kong between January 1, 2003, and December 31, 2018. | Pregnant women filling at least one prescription of quetiapine only (without other antipsychotic) during the first trimester of pregnancy, which is defined as the first 90 days after the last menstrual period (LMP). |
unexposed (general population or NOS)
Pregnant women who were not prescribed with any antipsychotic within the 90 days before the last menstrual period (LMP) and during the first trimester. |
191 / 464017 | Pregnancies with gestational age < 20 weeks, chromosomal abnormalities, fetal alcohol syndrome, abnormalities due to maternal infection, or exposure to known teratogens were excluded. |
Chan (Controls unexposed, sick), 2024 |
China 2003 - 2018 |
All pregnant women aged 15–50 years who gave a singleton live birth or stillbirth (≥20 weeks of gestation) in public hospitals in Hong Kong between January 1, 2003, and December 31, 2018. | Pregnant women filling at least one prescription of quetiapine only (without other antipsychotic) during the first trimester of pregnancy, which is defined as the first 90 days after the last menstrual period (LMP). |
unexposed, sick
Pregnant women with psychiatric diagnosis who were not prescribed with any antipsychotic within the 90 days before the last menstrual period (LMP) and during the first trimester. |
169 / 6476 | Pregnancies with gestational age < 20 weeks, chromosomal abnormalities, fetal alcohol syndrome, abnormalities due to maternal infection, or exposure to known teratogens were excluded. |
Cohen, 2023 |
USA 2008 - 2021 |
Pregnant women aged 18–45 years with lifetime histories of psychiatric illness. | Pregnant women with first trimester (0 <= 13 weeks) use of Quetiapine. |
unexposed, sick
Pregnant women unexposed to Second-generation antipsychotics (SGAs) during the entire pregnancy. |
264 / 886 | Overlapping: Cohen 2023 updates data of Cohen 2018 (major congenital malformations), based on a longer study period and more exposures. Univariate adjustments: choice to reporte results adjusted for alcohol use in 1st trimester. |
Ellfolk (Controls exposed to FGA), 2021 |
Finland 1996 - 2017 |
Singleton pregnancies ending in livebirth, stillbirth or elective termination of pregnancy due to fetal malformation. | Pregnant women who purchased second-generation antipsychotic quetiapine during 1 month before pregnancy until the end of first trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Pregnant women who purchased first-generation antipsychotic (F-GAs) during one month before pregnancy until the end of first trimester but did not purchase S-GAs during the same time period. |
2618 / 1030 | Overlapping: for Major, cardiac malformations and oral clefts: Ellfolk 2021 included in a larger study: Huybrechts 2023 (including Finland; 1996-2016) => outcomes not reported here. Stillbirths and gestational diabetes assessed in Ellfolk et al. 2019. |
Ellfolk (Controls unexposed NOS), 2021 |
Finland 1996 - 2017 |
Singleton pregnancies ending in livebirth, stillbirth or elective termination of pregnancy due to fetal malformation. | Pregnant women who purchased quetiapine during 1 month before pregnancy until the end of first trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
Pregnant women who had no purchases of second-generation antipsychotic (S-GAs) or first-generation antipsychotic (F-GAs) during three months before pregnancy until end of first trimester. |
2618 / 22540 | Overlapping: for Major, cardiac malformations and oral clefts: Ellfolk 2021 included in a larger study: Huybrechts 2023 (including Finland; 1996-2016) => outcomes not reported here. Stillbirths and gestational diabetes assessed in Ellfolk et al. 2019. |
Habermann (Control exposed to FGA), 2013 |
Germany 1997 - 2009 |
Subjects were enrolled through the consultation process at Teratology Information Service (TIS Berlin) | Women exposed to Quetiapine during pregnancy; comedication with First Generation Antipsycotics (FGA) was allowed. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Women exposed to First Generation Antipsychotics (FGAs) excluding comedication with Second Generation Antipsychotics (SGA) (cohort I). |
185 / 284 | Primary analyse on all Atypical Antipsychotics but Raw data are provided for some substances. Cases with potentially embryo- or fetotoxic drugs were not excluded for both the study cohort and the comparison cohort I but were assessed afterward. |
Habermann (Control unexposed, disease free), 2013 |
Germany 1997 - 2009 |
Subjects were enrolled through the consultation process at Teratology Information Service (TIS Berlin) | Women exposed to Quetiapine during pregnancy; comedication with First Generation Antipsycotics (FGA) was allowed. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, disease free
Women exposed to teratogenic, fetotoxic, or insufficiently studied agents were excluded as described elsewhere (cohort II). |
185 / 1122 | Primary analyse on all Atypical Antipsychotics but Raw data are provided for some substances. Cases with potentially embryo- or fetotoxic drugs were not excluded for both the study cohort and the comparison cohort I but were assessed afterward. |
Huybrechts (Controls unexposed, NOS), 2023 |
Denmark, Finland, Iceland, Norway, Sweden and USA. 1996 - 2018 |
All pregnancies resulting in singleton live-born infants (for Nordic cohorts) and publicly insured mothers linked to their live-born infants (for USA). | Pregnancies with 1 or more prescriptions of Quetiapine during the first trimester, the period for organogenesis. |
unexposed (general population or NOS)
Pregnancies who did not fill any antipsychotic prescriptions during the 3 months prior to pregnancy until the end of the first trimester. |
11065 / 6455324 | Overlapping: Data of Huybrechts 2016, Liu 2023 and Ellfolk 2021 totally and partially (major, cardiac, oral clefts) included in this larger study. Data of Reis 2008 (Sweden; 1995-2005) not included in Huybrechts 2023 (Sweden: 2006-2016). |
Huybrechts (Controls unexposed, sick), 2023 |
Denmark, Finland, Iceland, Norway, Sweden and USA. 1996 - 2018 |
All pregnancies resulting in singleton live-born infants (for Nordic cohorts) and publicly insured mothers linked to their live-born infants (for USA). | Pregnancies with 1 or more prescriptions of Quetiapine during the first trimester, the period for organogenesis. |
unexposed, sick
Pregnancies in women with mental health condition, who did not fill any antipsychotic prescriptions during the 3 months prior to pregnancy until the end of the first trimester. |
8350 / 318731 | Overlapping: Data of Huybrechts 2016, Liu 2023 and Ellfolk 2021 totally and partially (major, cardiac, oral clefts) included in this larger study. Data of Reis 2008 (Sweden; 1995-2005) not included in Huybrechts 2023 (Sweden: 2006-2016). |
Källen, 2013 |
Sweden 1996 - 2011 |
Nearly all births in Sweden and is based on standardized medical records, used in the whole country | Pregnant women exposed to Quetiapine. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
Not specified |
75 / -9 | The study was related to the Central Nervous System (CNS) active drugs. RR calculated with observed/expected numbers. All outcomes are provided for neuroleptics as a whole excepted for preterm (2nd generation antipsychotics). |
Kananen, 2023 |
Finland 2002 - 2016 |
Women who gave birth (at gestational week ≥22 or birth weight ≥500g) at Kuopio University Hospital between 2002 and 2016. | All pregnant women who either self-reported the use or were administered quetiapine at the Kuopio University Hospital (KUH). |
unexposed (general population or NOS)
All pregnant women without antipsychotic exposure. |
153 / 35837 | OR based on 152 and 35133 exposed and unexposed pregnancy, respectively (values excluding multifetal gestations and antiemetics users). Quetiapine with other antipsychotic agent: 3.7%. |
Kulkarni, 2024 |
Australia 2005 - 2019 |
Women who were pregnant or had a baby in the last 12 months, taking antipsychotic medication during pregnancy, and living in Australia. | Women who had a diagnosis of a schizophrenia spectrum disorder and took quetiapine during the first trimester of pregnancy (at minimum). |
unexposed, sick
Women with a diagnosis of schizophrenia spectrum disorder who chose not to take any antipsychotic during the first trimester of pregnancy (at a minimum). |
53 / 24 | Authors studied 2 atypical antipsychotics => To avoid redundancy of controls only one is used in the class meta-analysis, this one with the highest number of exposed pregnancies. |
McKenna, 2005 |
Canada, Israel and England Not specified |
Women who contacted the line for information. | Women who has taken Quetiapine within 3 months of pregnancy or during pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, disease free
Subsequent woman who contacted the TIS regarding exposure to a non-teratogenic agent. Women who reported a psychiatric diagnosis or psychotropic medication use were excluded from the comparison group. |
36 / 151 | All of the women were exposed in the first trimester. |
Newport, 2007 |
USA Not specified |
Pregnant women treated with antipsychotics recruited from the Emory Women’s Mental Health Program. | Pregnant women receiving receiving a stable daily dose of Quetiapine for >5 elimination half-lives at delivery. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Pregnant women receiving Haloperidol. |
21 / 13 | Each substance is a subanalyse. The meta-analysis authors considered Atypic antipsychotics as the exposed group and Haloperidol as the control group. In the original publication, the authors provided each outcome by Substance. |
Ozturk, 2016 |
Turkey 2007 - 2012 |
Women referred to our prenatal consultation service for psychotropic drug exposure. | Pregnancies exposed to Quetiapine. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
Pregnancies not exposed to known teratogens, in the same year applying the same procedure for data collection and follow-up. |
8 / 275 | Authors investigated Psychotropic drugs as a whole but also provided data for individual substances. Drug exposures took place in 81% during the first trimester, and 11% in all three trimesters. Distinction between miscarriage and stillbirth. |
Park, 2018 |
USA 2000 - 2010 |
Women who during the 3 months before their last menstrual period filled a prescription for one of the five most frequently used atypical antipsychotics: aripiprazole, olanzapine, quetiapine, risperidone, or ziprasidone. | Pregnant women who had two or more prescriptions dispensed during the first 140 days of their pregnancy for Quetiapine (also received before pregnancy). Exclusion if more than 1 studied antipsychotic. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, sick
Pregnant women who had no prescriptions dispensed for an anti- psychotic medication during the first 140 days of pregnancy were classified as “discontinuers.” |
1542 / 2951 | Primary analyses performed individually for each substance ( aripiprazole, olanzapine, quetiapine, risperidone, or ziprasidone). |
Peng, 2013 |
China 2007 - 2010 |
Women with singleton pregnancy at more than 38 weeks who were seeking prenatal care in the department of the Second Xiangya Hospital. | Women with a diagnosis of schizophrenia who were taking quetiapine throughout the pregnancy. |
unexposed, disease free
Women who not have any mental disorder and were not treated with any antipsychotics in the same department. |
6 / 76 | Continuous variables: there were no significant differences between the two groups in the Apgar score at 1 and 5 min, as well as the mean weight, height, and brain circumference. |
Raguideau, 2017 |
France 2011 - 2015 |
All pregnancies ending between 2011 and 2015, regardless of the outcome (live birth, stillbirth or therapeutic abortions after 22 WA), were eligible for inclusion. | Pregnancies exposed Quetiapine during the two first months of pregnancy (reimbursement occurring the month before the pregnancy or during the two first months of pregnancy). (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
Pregnancies not exposed to bipolar disorder drugs during the two first months of pregnancy (reimbursement occurring the month before the pregnancy or during the two first months of pregnancy). |
219 / 1888130 | The study not considered all major malformations but 26 malfo. |
Reis (Control exposed to FGA), 2008 |
Sweded 1995 - 2005 |
Whole country (1.4% of all deliveries in Sweden are missing in the register). | Women who had reported the use of Quetiapine in early pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Women who had reported the use of 'Any first-generation antipsychotic' in early pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
4 / 435 | Atypical and typical antipsychotics are subgroups of the entire study. Atypical versus Typical. OR and adjustement performed for other groups. Relative severe malformations, with exclusion of known chromosome anomalies. |
Reis (Unexposed control, NOS), 2008 |
Sweden 1995 - 2005 |
Whole country (1.4% of all deliveries in Sweden are missing in the register). | Women who had reported the use of Quetiapine in early pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
All other women in the register. |
4 / 958729 | Atypical antipsychotics are a subgroup of the entire study. OR and adjustement performed for other groups. Relative severe malformations, with exclusion of known chromosome anomalies. |
Sadowski, 2013 |
Canada 2005 - 2009 |
Women who directly contacted the Motherisk Program at the Hospital for Sick Children in Toronto, Canada. | Women who confirmed the use of Quetiapine for a minimum of 4 weeks of pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, disease free
Women who reported exposure to non-teratogenic agents (eg, acetaminophen, antihistamines, etc). Control women who reported a history of psychiatric disorders or who were exposed in their current pregnancy to a known teratogen were excluded. |
94 / 133 | Women who were exposed to teratogenic medications unrelated to their psychiatric disorder treatment, such as acutane, or who abused substances (eg, alcohol, marijuana, cocaine, heroin, etc) were excluded from the study cohort. |
Sorensen, 2015 |
Denmark 1997 - 2008 |
Pregnancies registered in the nationwide Danish registries from 1997 to 2008 (N = 1,005,319) | Any prescription of Quetiapine redeemed by the pregnant women during the exposure window, and recorded in the Danish National Prescription Register. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
Unexposed women were defined as pregnant women who did not redeem any prescription of antipsychotic medications during the exposure window. |
174 / 841183 | Primary analyses performed on antipsychotics versus unexposed. Authors also analysed each antipsychotic (typical and atypical) substance separately. |
Straub, 2022 |
USA 2000 - 2015 |
Mothers (12-55 years old) who were continuously insured from 3 months before until 1 month after pregnancy. | Children whose mother filled a prescription for Quetiapine during the second half of pregnancy (>18 gestational weeks). (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
Children born to mothers with no antipsychotic dispensing from 90 days before pregnancy until birth. |
4457 / 3309095 | Estimates from both cohorts were combined through meta-analysis by authors. Children with a known chromosomal or genetic abnormality were excluded. |
Vigod, 2015 |
Canada 2003 - 2012 |
All women who delivered a singleton infant (live birth or stillbirth) in Ontario during the study period registered in health administrative databases housed at the Institute for Clinical Evaluative Sciences (ICES) in Toronto. | At least two consecutive prescriptions for Quetiapine filled between the conception date and the delivery date. At least one prescriptions filled prior to 27 GW. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, sick
Matched women not exposed to any antipsychotic drug during pregnancy using a HDPS matching algorithm to minimise treatment selection bias (leading to similar psychiatric diagnoses before index pregnancy => considered as 'unexposed, sick'). |
556 / 1021 | Atypical antipsychotic drugs (and each substance) are a subgroup of the primary analysis on the antipsychotic drug. For those results, RRadj only provided on a graphic but raw data are provided by authors and used for this meta analysis. |
Wang - HK cohort, 2021 |
China 2001 - 2015 |
Primiparous pregnancies resulting in a live or stillbirth among the entire pregnancy population of the Clinical Data Analysis and Reporting System (CDARS; representing 165 hospitals/institutions) aged between 15 and 50 years old during the study period. | Pregnant women who received at least 56 days coverage time of prescriptions of Quetiapine before and during pregnancy (continuers). |
unexposed, sick
Pregnant women who did not receive any antipsychotic during pregnancy, but did before pregnancy (discontinuers). |
-9 / 340 | Number of quetiapine continuers not provided by authors. |
Wang - UK cohort, 2021 |
United Kingdom 1990 - 2017 |
Primiparous pregnancies resulting in a live or stillbirth among the entire pregnancy population of the Health Improvement Network (THIN; representing over 6% of the UK population) aged between 15 and 50 years old during the study period. | Pregnant women who received at least two prescriptions (normally 28 days for one prescription) of Quetiapine before and during pregnancy (continuers). |
unexposed, sick
Pregnant women who did not receive any antipsychotic during pregnancy, but did before pregnancy (discontinuers). |
-9 / 1577 | Number of quetiapine continuers not provided by authors. |
Wurtz, 2017 |
Denmark 1997 - 2012 |
All singleton live-born children in Denmark from January 1, 1997 to December 31, 2012. | Any prescription of Quetiapine registered during the exposure window (defined as 30 days before the estimated first day of the last menstrual period to the day before birth). (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
No prescription of antipsychotic medication registered in the Danish Register of Medicinal Product Statistics during the exposure window (defined as 30 days before the estimated first day of the last menstrual period to the day before birth). |
-9 / 960527 | The exposure of interest was the mother’s use of Antipsychotic (AP) during pregnancy. Second generation antipsychotic, quetiapine and olanzapine are subanalyses. |
Yaris, 2005 |
Turkey 1999 - 2004 |
Pregnant women calling for a counseling about the teratogenic risks of drugs, chemicals, and X-ray. | Women who were exposed to Quetiapine during pregnancy for depression, anxiety, and psychotic disorders. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed (general population or NOS)
Women who did not use any drug while pregnant. |
2 / 248 | Multiple drug exposure. Raw data for Intrauterine exitus not reported because the nb of cases in the unexposed group not clearly stated. |
Study | Country Study period |
Case | Control | Sample size | Rmk |
---|---|---|---|---|---|
Ishikawa, 2024 |
Japan 2005 - 2022 |
Women whose pregnancies ended in a miscarriage that occurred between the beginning of the fourth and 22nd weeks of gestation. | Women randomly selected from the entire cohort of pregnancies by risk-set sampling with replacement and were individu- ally matched to the cases (3:1). | 44118 / 132317 | Exposure to benzodiazepines was used as a positive control. |