Methyldopa (versus unexposed)

Exposed non-exposed studies (cohort)

Study Country
Study period
Population source Exposure definition Non-exposure definition Sample size Rmk
Al Khalaf (Controls unexposed, disease free), 2022 United Kingdom
1997 - 2016
Women with complete pregnancies, with a minimum length of 20 weeks’ gestation, that consented to linkage with Hospital Episodes Statistics (HES). Women with at least 1 prescription of Methyldopa for chronic hypertension (diagnosis of hypertension recorded during a consultation in primary care or hospitalization, or inferred hypertension if they received repeat prescriptions of Blood pressure (BP) lowering-medication or based on BP readings). unexposed, disease free
Untreated women without chronic hypertension.
1952 / 1739944
Al Khalaf (Controls unexposed, sick), 2022 United Kingdom
1997 - 2016
Women with complete pregnancies, with a minimum length of 20 weeks’ gestation, that consented to linkage with Hospital Episodes Statistics (HES). Women with at least 1 prescription of Methyldopa for chronic hypertension (diagnosis of hypertension recorded during a consultation in primary care or hospitalization, or inferred hypertension if they received repeat prescriptions of Blood pressure (BP) lowering-medication or based on BP readings). unexposed, sick
Women with chronic hypertension, not treated.
1952 / 7809 Pregnant women who had prescriptions for multiple antihypertensive medications or switched to other agent(s) at any stage of pregnancy were excluded when comparing agent versus agent.
Chan, 2010 Canada
1997 - 2002
Pregnant women who had contacted the Motherisk Program for counseling of medication safety during pregnancy. Children of women treated with Methyldopa for hypertension during pregnancy. unexposed, disease free
Children of normotensive women exposed to non-teratogenic substance during pregnancy.
25 / 42 Mothers were excluded if they used the medications of interest for less than three weeks, or were exposed to a second anti-hypertensive agent or to a known teratogen (e.g., isotretinoin, phenytoin).
Fidler, 1983 United Kingdom (UK)
Not specified.
All the women booked for delivery at Queen Charlotte's Maternity Hospital who had diastolic blood pressure of at least 95mm Hg on two separate occasions at least 24 hours apart or greater than105mm Hg on one occasion. Hypertensive pregnant patients allocated at random to receive methyldopa (250mg 3 times a day and increased until 3g a day if necessary). unexposed, disease free
Normotensive pregnant women with the nearest hospital reference number after that of the index patient, matched for parity and gestational age at delivery.
50 / 96 Considered as a prospective cohort rather than a randomized control because patients were randomly allocated to methyldopa or oxprenolol but the Normotensive control group not randomly selected.
Hoeltzenbein, 2017 Germany
2000 - 2014
Pregnancies that called the German Embryotox institute for risk assessment on drug use during pregnancy. Pregnancies with chronic hypertension, exposed to methyldopa in the first trimester (gestational week 12 plus 6 days after last menstrual period). unexposed, disease free
Pregnancies without a diagnosis of chronic hypertension and without antihypertensive therapy, randomly selected in the database.
261 / 526 Overlapping between Kayser 2020 and Hoeltzenbein 2017 for 2 outcomes (preterm/stillbirth) => about the same number of pregnancies, thus use of data with the most relevant period of exposure (2nd/3rd trimester of exposure), i.e Kayser 2020.
Ishikawa (Controls unexposed, disease free), 2023 Japan
2010 - 2019
Pregnant women with chronic hypertension Pregnant women with chronic hypertension and prescribed Methyldopa in the first trimester. unexposed, disease free
Pregnant women without hypertensive disorders in the first trimester.
93 / 74213
Ishikawa (Controls unexposed, sick), 2023 Japan
2010 - 2019
Pregnant women with chronic hypertension Pregnant women with chronic hypertension and prescribed Methyldopa in the first trimester. unexposed, sick
Pregnant women chronic hypertension but no first-trimester antihypertensive prescriptions.
93 / 1007
Kayser, 2020 Germany
2001 - 2015
Pregnancies for which Embryotox service was contacted for risk assessment on drug use in pregnancy. Pregnancies in hypertensive women treated with methyldopa after the first trimester, but not on beta-blockers at any time during pregnancy. Methyldopa exposure may have started before the second trimester. unexposed, disease free
Pregnancies in women without hypertension and without any antihypertensive therapy at any time during pregnancy.
221 / 580 Overlapping between Kayser 2020 and Hoeltzenbein 2017 for 2 outcomes (preterm/stillbirth) => about the same number of pregnancies, thus use of data with the most relevant period of exposure (2nd/3rd trimester of exposure), i.e Kayser 2020.
Leather, 1968 United Kingdom
Not specified.
Patients that were referred from the antenatal clinics and from obstetric wards, diagnosed with early (before 20 weeks of gestation) or late (normontensive before 20 weeks) hypertension. Pregnant patients with early hypertension (before 20 gestational weeks) randomly allocated to treatment group, i.e bendrofluazide 5-10 mg daily with potassium supplements and methyldopa 0-5-2g daily in divided doses. unexposed, sick
Pregnant patients with early hypertension (before 20 gestational weeks) randomly allocated to control group.
23 / 24 Data related to chronic hypertension were reported here.
Mabie, 1986 USA
1980 - 1984
Pregnant women with chronic hypertension (>= 140/90 mmHg before pregnancy or at less than 20 week's gestation) who delivered at this hospital during the study period. Pregnant women with chronic hypertension treated with Methylopa only. unexposed, sick
Pregnant women with chronic hypertension without treatment.
54 / 82 Data on Methyldopa only reported rather than co-administration Methyldopa and hydrochlorothiazide.
Orbach, 2013 Israel
1998 - 2008
Women from 15-49 years old who were registered with Clalit and who lived in the southern district of Israel who gave birth at Soroka Medical Center (SMC). Pregnant women with Methyldopa dispensed during the third trimester of pregnancy. unexposed, disease free
All pregnant women without diagnosis of chronic hypertension and who were not exposed to antihypertensive drugs through the first or the third trimester during the study period.
340 / 97820 Chromosomal diseases were excluded. Five hundred fifteen infants who were exposed to antihypertensive drugs in utero for maternal indications other than hypertension were excluded from the cohort.
Redman, 1976 United Kingdom
Not specified.
Pregnant women with moderate hypertension detected before 28 gestational weeks in the routine antenatal clinics. Pregnant women with moderate hypertension detected before 28 gestational weeks randomly allocated to the Methyldopa group. unexposed, sick
Pregnant women with moderate hypertension detected before 28 gestational weeks randomly allocated to no treatment group.
107 / 101 Patients separated into early or late group, if hypertension was detected before or after 28 weeks => After 28 weeks probably mainly pregnancy-induced hypertension => Thus, here use of data of 'early' groups.
Sibai, 1990 USA
Not specified
Pregnant patients with mild to moderate chronic hypertension ascertained at 6 to 13 weeks' gestation at the E.H. Crump Women's Hospital. Pregnant patients with mild to moderate chronic hypertension randomly allocated to methyldopa (start at 750 mg/day and maximum of 4 g/day). unexposed, sick
Pregnant patients with mild to moderate chronic hypertension randomly allocated to no medications.
88 / 90 Because pregnancies were exposed to anti-hypertensives before randomisation => outcomes potentially impacted by exposure during first trimester (superimposed pre-eclampsia, SGA, preterm, LBW, abruptio placentae and perinatal death) are not reported here.
Vaclavik, 2024 The Czech Republic
2012 - 2022
All births and abortions in the period 2012 - 2022 in the Czech Republic. Births whose mothers were prescribed Methyldopa during pregnancy (for pre-existing hypertension or pregnancy-induced hypertension). unexposed, disease free
Births whose mothers had no hypertension.
-9 / -9
Weitz, 1987 USA
Not specified
Singleton pregnancy (< 34 gestational age) in women with presumed chronic hypertension (140/90 mmHg). Pregnant women allocated into the treatment group: methyldopa one tablet (250 mg) per os twice in day (tid). These doses were increased every 48 h as needed to a maximum of 2 tablets qid. unexposed, sick
Pregnant women allocated into the placebo group: one tablet per os twice in day (tid). These doses were increased every 48 h as needed to a maximum of 2 tablets qid.
13 / 12 Other antihypertensive medications were utilized only if severe superimposed pre--eclampsia developed. In that case, hydralazine and magnesium sulfate were administered, and the patient delivered.
Welt, 1981 USA
Not specified.
Pregnant women with underlying hypertensive disease elected to join a protocol of intensified prenatal care and prophylactic drug therapy. Pregnant women with underlying hypertensive disease randomly and blindly assigned to methyldopa group (250 mg 3 times per day). unexposed, sick
Pregnant women with underlying hypertensive disease randomly and blindly assigned to placebo group (3 times per day).
6 / 6 The main results were provided for non randomized group versus randomized group (whatever treatment in the group). The only reported results are those of randomized group, with distinction between treatment (provided in the text, not in the tables).

Case-control studies (cohort)

Study Country
Study period
Case Control Sample size Rmk
De Jonge, 2013 The Netherlands
1998 - 2008
All malformed foetuses and children (live births, stillbirths, spontaneous abortions and terminations of pregnancy) excluding chromosomal and genetic disorders. From the InterAction Database (IADB), a population-based prescription database that contains prescription data from approximately 55 community pharmacies in The Netherlands, we selected the population controls. The IADB covers an estimated population of 500,000 individuals, which is considered representative of the general population. 3212 / 29223
Fisher (Controls unexposed, disease free), 2017 USA
1997 - 2011
Cases of cardiovascular malformations in live births, fetal deaths occurring after 20 weeks, and elective pregnancy terminations. (According to Caton 2009) Nonmalformed live births randomly selected from birth certificates or hospital discharge records in each study site. 10625 / 11137 Overlapping: Fisher 2017 included all data published by Caton 2009 based on a longer period study (1997-2011 versus 1977-2003), more cases, more outcomes and 2 control groups. Thus Fisher 2017 was used rather than Caton 2009.
Fisher (Controls unexposed, sick), 2017 USA
1997 - 2011
Cases of cardiovascular malformations in live births, fetal deaths occurring after 20 weeks, and elective pregnancy terminations. (According to Caton 2009) Nonmalformed live births randomly selected from birth certificates or hospital discharge records in each study site. 10625 / 11137 Overlapping: Fisher 2017 included all data published by Caton 2009 based on a longer period study (1997-2011 versus 1977-2003), more cases, more outcomes and 2 control groups. Thus Fisher 2017 was used rather than Caton 2009.
Medveczky, 2004 Hungary
1980 - 1996
Newborn infants (including infant deaths and usual stillborn fetuses) with Neural tube defects with non-syndromic (i.e. isolated anencephaly, spina bifida aperta/cystica, encephalocele). Newborn infants (including infant deaths and usual stillborn fetuses) without congenital abnormalities. 1202 / 38151 Study design completed with other studies published on the Hungarian Case-Control Surveillance of Congenital Abnormalities (HCCSCA).
Van Zutphen, 2014 USA
1997 - 2009
All cases (liveborn, stillborn after 20 weeks gestation, or induced abortions) with severe hypospadias (ie, subcoronal or penile, scrotal, or perineal meatal opening) diagnosed at the time of physical examination, surgery, or autopsy. Male live births without birth defects randomly selected from birth certificates or hospital discharge listings in the same population as the case neonates. 2131 / 5129 Mothers reporting antihypertensive medications for the treatment of other indications (eg, b-blockers for migraine headaches) were excluded from the analyses. Overlapping: Caton 2008 (1997-2002) totally included in Van Zutphen 2014 (1997-2009).

master protocol