Study | Country Study period Study design |
Data source | Exposure definition | Non-exposure definition | Exposition period | Sample size (exposed/unexposed) Or (case / control) |
Remarks | Risk of bias |
---|---|---|---|---|---|---|---|---|
Battino 2024 |
Worldwide (47 countries) 1999 - 2022 prospective cohort |
The International Registry of Antiepileptic Drugs and Pregnancy (EURAP). | Pregnant women with epilepsy exposed to Zonisamide monotherapy at the time of conception. |
exposed to other treatment, sick
Pregnant women with epilepsy exposed to lamotrigine monotherapy at the time of conception. |
early pregnancy | 29 / 3584 | Overlapping: Battino 2024 (1999-2022) updates and totally includes Tomson 2018 (1999-2016) and Jimenez 2020 (1 center in Spain 2000-2018) => Use of Battino 2024 for the 8 (plus 16 in eSupp) ASM monotherapies studied here. | |
Reporting physicians collected information on drug therapy after each trimester. | ||||||||
Hernández-Díaz (Zonisamide) 2017 |
United States and Canada 1997 - 2017 prospective cohort |
The North American Antiepileptic Drug Pregnancy Registry | Infants born to women who used zonisamide in monotherapy throughout pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Infants born to women who used lamotrigine in monotherapy throughout pregnancy. |
throughout pregnancy | 125 / 1799 | 'Most women used their AED throughout pregnancy. The exception was topiramate'. The main indications for AED were epilepsy (91%). | |
Women were questioned with a computer-assisted telephone interview 3 times. | ||||||||
Hernández-Díaz (Zonisamide) (Controls exposed to Lamotrigine, sick) 2012 |
North America and Canada 1997 - 2011 prospective cohort |
The North American Antiepileptic Drug Pregnancy Register and the Active Malformations Surveillance Program. | Infants of pregnant women who used zonisamide for epileptic indication as monotherapy, during the first 4 lunar months after the last menstrual period (equal 16 weeks of gestation). (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Infants of pregnant women who used lamotrigine for mixed indications as monotherapy, during the first 4 lunar months after the last menstrual period (equal 16 weeks of gestation). |
1st trimester | 90 / 1562 | Less than 90% of women are taking Lamotrigine for epilepsy. | |
Women were questioned with a computer-assisted telephone interview 3 times. | ||||||||
Hernández-Díaz (Zonisamide) (Controls exposed to Lamotrigine, sick) 2014 |
United States and Canada 1997 - 2012 prospective cohort |
The North American Antiepileptic Drug Pregnancy Register | Infants of women exposed to zonisamide for epileptic indication as monotherapy throughout pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Infants of women exposed to lamotrigine for mixed indications as monotherapy throughout pregnancy. |
throughout pregnancy | 98 / 1581 | Less than 90% of women are taking Lamotrigine for epilepsy. A more recent publication Hernández-Díaz 2017 gives a better review of the outcome 'small for gestational age'. Most women used their antiepileptic drug throughout pregnancy. | |
Women were questioned with a computer-assisted telephone interview 3 times. | ||||||||
Hernández-Díaz (Zonisamide) (Controls unexposed, disease free) 2012 |
North America and Canada 1997 - 2011 prospective cohort |
The North American Antiepileptic Drug Pregnancy Register and the Active Malformations Surveillance Program. | Infants of pregnant women who used zonisamide for epileptic indication as monotherapy, during the first 4 lunar months after the last menstrual period (equal 16 weeks of gestation). (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, disease free
Infants of pregnant women, not taking an antiepileptic drug and without epilepsy, who were recruited from among the friends and family members of the enrolled women taking an antiepileptic drug. |
1st trimester | 90 / 442 | ||
Women were questioned with a computer-assisted telephone interview 3 times. | ||||||||
Hernández-Díaz (Zonisamide) (Controls unexposed, disease free) 2014 |
United States and Canada 1997 - 2012 prospective cohort |
The North American Antiepileptic Drug Pregnancy Register | Infants of women exposed to zonisamide as monotherapy throughout pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, disease free
Infants of pregnant women not taking an antiepileptic drugs and without epilepsy who had been recruited among the friends and relatives of antiepileptic drugs-exposed participants. |
throughout pregnancy | 98 / 457 | Most women used their antiepileptic drug throughout pregnancy. A more recent publication (Hernández-Díaz 2017) gives a better review for the outcome 'small for gestational age'. | |
Women were questioned with a computer-assisted telephone interview 3 times. | ||||||||
Meador (Zonisamide) (Controls exposed to Lamotrigine, sick) 2021 |
US 2012 - 2016 prospective cohort |
The Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) study (20 US tertiary epilepsy centers). | Children with epileptic mothers using zonisamide monotherapy in the third trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Children with epileptic mothers using lamotrigine monotherapy in the third trimester. |
3rd trimester | 11 / 93 | Exclusion criteria included history of psychogenic nonepileptic spells, expected IQ of less than 70, other major medical illness, and switching of ASMs in pregnancy before enrollment. | |
Data were collected from participants using a daily electronic diary that was verified at study visits and with medical records. | ||||||||
Meador (Zonisamide) (Controls exposed to Lamotrigine, sick) 2020 |
US 2012 - 2016 prospective cohort |
The Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) study (20 US tertiary epilepsy centers). | Children born to pregnant women with epilepsy exposed to zonisamide monotherapy during the first trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Children born to pregnant women with epilepsy exposed to lamotrigine monotherapy during the first trimester. |
1st trimester | 13 / 113 | ||
Data were obtained from participants and their medical records. | ||||||||
Meador (Zonisamide) (Controls unexposed, disease free) 2021 |
US 2012 - 2016 prospective cohort |
The Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) study (20 US tertiary epilepsy centers). | Children with epileptic mothers using zonisamide monotherapy in the third trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, disease free
Children of healthy women. |
3rd trimester | 11 / 106 | Exclusion criteria included history of psychogenic nonepileptic spells, expected IQ of less than 70, other major medical illness, and switching of ASMs in pregnancy before enrollment. | |
Data were collected from participants using a daily electronic diary that was verified at study visits and with medical records. | ||||||||
Meador (Zonisamide) (Controls unexposed, disease free) 2020 |
US 2012 - 2016 prospective cohort |
The Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) study (20 US tertiary epilepsy centers). | Children born to pregnant women with epilepsy exposed to zonisamide monotherapy during the first trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, disease free
Children born to healthy pregnant women. |
1st trimester | 13 / 106 | ||
Data were obtained from participants and their medical records. | ||||||||
Meador (Zonisamide) (Controls unexposed, sick) 2020 |
US 2012 - 2016 prospective cohort |
The Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) study (20 US tertiary epilepsy centers). | Children born to pregnant women with epilepsy exposed to zonisamide monotherapy during the first trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, sick
Children born to pregnant women with epilepsy with no antiepileptic drug use. |
1st trimester | 13 / 15 | ||
Data were obtained from participants and their medical records. | ||||||||
The Kerala Registry for Epilepsy and Pregnancy (Epilepsy) (Controls exposed to Lamotrigine) 2024 |
India 1998 - 2023 prospective cohort |
The Kerala Registry of Epilepsy and Pregnancy (KREP) | Children of women with epilepsy using Zonisamide monotherapy any time during the first trimester of pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Children of women with epilepsy using lamotrigine monotherapy any time during the first trimester of pregnancy. |
1st trimester | 3 / 50 | Data extracted from the publication Perucca 2024, an update of the Epilepsy-pregnancy registries. Study design and control data based on Thomas et al., 2017 and Thomas et al., 2021. | |
Women were instructed to record the use of the antiepileptic drugs on a daily basis in the pregnancy diary that was given to them. | ||||||||
The Kerala Registry for Epilepsy and Pregnancy (Epilepsy) (Controls unexposed, sick) 2024 |
India 1998 - 2023 prospective cohort |
The Kerala Registry of Epilepsy and Pregnancy (KREP) | Children of women with epilepsy using Zonisamide monotherapy any time during the first trimester of pregnancy. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, sick
Children of women with epilepsy not using any antiepileptic drugs during the first trimester. |
1st trimester | 3 / 340 | Data extracted from the publication Perucca 2024, an update of the Epilepsy-pregnancy registries. Study design and control data based on Thomas et al., 2017 and Thomas et al., 2021. | |
Women were instructed to record the use of the antiepileptic drugs on a daily basis in the pregnancy diary that was given to them. | ||||||||
The UKIEPR (Epilepsy) (Controls exposed to Lamotrigine) 2024 |
UK and Ireland 1996 - 2023 prospective cohort |
The United Kingdom Epilepsy and Pregnancy Register | Infants of women with epilepsy exposed to Zonisamide in monotherapy during the first trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
exposed to other treatment, sick
Infants of women with epilepsy exposed to lamotrigine in monotherapy during the first trimester. |
1st trimester | 25 / 2098 | Data extracted from the publication Perucca 2024, an update of the Epilepsy-pregnancy registries. Study design based on Morrow 2006 and Campbell 2014. | |
Information was collected at registration and changes of antiepileptic drugs during pregnancy were detected during the follow-up duration by sending a standardised questionnaire to the patient's general practitioner. Other health care practitioners were contacted if identified. | ||||||||
The UKIEPR (Epilepsy) (Controls unexposed, sick) 2024 |
UK and Ireland 1996 - 2023 prospective cohort |
The United Kingdom Epilepsy and Pregnancy Register | Infants of women with epilepsy exposed to Zonisamide in monotherapy during the first trimester. (This is a subgroup of exposure among the whole exposed group considered in the study). |
unexposed, sick
Infants of women with epilepsy on no antiepileptic drugs during pregnancy. |
1st trimester | 25 / 541 | Data extracted from the publication Perucca 2024, an update of the Epilepsy-pregnancy registries. Study design based on Morrow 2006 and Campbell 2014. | |
Information was collected at registration and changes of antiepileptic drugs during pregnancy were detected during the follow-up duration by sending a standardised questionnaire to the patient's general practitioner. Other health care practitioners were contacted if identified. |
Study | Country Study period Study design |
Data source | Case | Control | Exposition | Exposition period | Sample size (exposed/unexposed) Or (case / control) |
Remarks | Risk of bias |
---|
Risk of bias: : NA; : low; : moderate; : serious; : critical; : unclear;