Bisoprolol (versus unexposed)

Exposed non-exposed, cohort studies

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
Delteil
2024
France
2004 - 2021
retrospective cohort (claims database)
EFEMERIS (Évaluation chez la Femme Enceinte des MÉdicaments et de leurs RISques) database, and the Registre des Handicaps de l'Enfant en Haute-Garonne (RHE31), Haute-Garonne, France. Pregnancies with at least one dispensed prescription of Bisoprolol during pregnancy (between last menstrual period and delivery). unexposed (general population or NOS)
Pregnancies without dispensed prescription of beta-blockers and other anti-hypertensive agents during pregnancy.
at least 1st trimester 93 / 172284 When available, data in women with chronic pathology (hypertension or cardiac), treated at least during the 1st trimester were preferred to all indications (including gestational hypertension, ...). Exposure at least T1 considered as chronic indications.
Women's drug exposure during pregnancy was estimated on the basis of dispensed prescription drugs recorded by the French Assurance Maladie.
Fitton (Controls unexposed, disease free)
2020
Scotland
2010 - 2014
retrospective cohort (claims database)
Linkage of 4 Scottish healthcare databases, held by the Information Statistics Division. All women who had a singleton birth and who were dispensed at least one prescription for Bisoprolol during the 300 days before birth (whatever the indication). unexposed, disease free
All women who had a singleton birth during the same study period who were not dispensed antihypertensive medication during or 60 days following pregnancy, and who did not have an ICD-10 code for hypertension (chronic, gestational, or unspecified hypertension).
during pregnancy (anytime or not specified) 106 / 250693 The majority of offspring were exposed to a β-blocker only (58.66%, 4003 children), calcium channel blockers only (8.18%, 558 children), or a combination of >1 antihypertensive medication (20.53%, 1403 children).
The Prescribing Information System which collects information on encashed prescriptions issued by primary care and dispensed from community pharmacies for all Scottish residents.
Fitton (Controls unexposed, sick)
2020
Scotland
2010 - 2014
retrospective cohort (claims database)
Linkage of 4 Scottish healthcare databases, held by the Information Statistics Division. All women who had a singleton birth and who were dispensed at least one prescription for Bisoprolol during the 300 days before birth (whatever the indication). unexposed, sick
All women who had a singleton birth during the same study period, who had an ICD-10 code for hypertension (chronic, gestational, or unspecified hypertension) and who were not dispensed antihypertensive medication at any stage during or 60 days after pregnancy.
during pregnancy (anytime or not specified) 106 / 7971 The majority of offspring were exposed to a β-blocker only (58.66%, 4003 children), calcium channel blockers only (8.18%, 558 children), or a combination of >1 antihypertensive medication (20.53%, 1403 children).
The Prescribing Information System which collects information on encashed prescriptions issued by primary care and dispensed from community pharmacies for all Scottish residents.
Hoeltzenbein
2018
Germany
2000 - 2015
prospective cohort
The German Embryotox pharmacovigilance institute. Pregnancies with bisoprolol exposure at least during the first trimester. Concomitant therapy with other antihypertensive drugs except angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) was possible. unexposed, disease free
Nonhypertensive pregnancies, without use of beta-blockers and other antihypertensives during pregnancy, randomly selected.
at least 1st trimester 339 / 678 The most frequent treatment indications for bisoprolol were hypertension (203/339, 60%) and arrhythmias (115/ 339, 34%). The daily dose was within the recommended range [median 5 mg; min–max 1.25–20mg; information available in 295/339 pregnancies].
At the initial contact (during pregnancy) maternal characteristics and detailed exposure assessment are asked for after informed consent. The outcome of pregnancy was not known at the time of enrollment.
Ishibashi
2017
Japan
2000 - 2016
retrospective cohort
15 Japanese institutions. Pregnancies in long QT patients with Bisoprolol therapy. unexposed, sick
Pregnancies in long QT patients without β-blocker therapy.
during pregnancy (anytime or not specified) 10 / 94 Exposure: 10 bisoprolol (5mg/day, 0.072±0.028mg/kg/day).
All data were collected with checking their maternity record book.
Tanaka
2016
Japan
2000 - 2010
retrospective cohort
The National Cerebral and Cardiovascular Center in Osaka, Japan. Pregnant women with cardiovascular disease treated with Atenolol for at least 2 weeks before delivery. unexposed, sick
Pregnant women with cardiovascular disease who were not treated with an oral α/β- or β-adrenergic blocker randomly identified over the same period.
during pregnancy (anytime or not specified) 5 / 100 Maternal cardiovascular diseases: congenital heart disease and pulmonary hypertension; aortic disease; valvular heart disease; coronary artery disease and acute coronary syndrome; cardiomyopathy and heart failure; and arrhythmia.
Patient data were collected from their medical records and included medication(s) used (β-blockers and other ones).
Vaclavik
2024
The Czech Republic
2012 - 2022
population based cohort retrospective
The National Registry of Reproductive Health (NRRZ) and the National Registry of Reimbursable Health Services (NRHZS). Births whose mothers were prescribed Bisoprolol during pregnancy (for pre-existing hypertension or pregnancy-induced hypertension). unexposed, disease free
Births whose mothers had no hypertension.
during pregnancy (anytime or not specified) -9 / -9
The National Registry of Reimbursable Health Services (NRHZS).

Case-control studies

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;  

Empty. There are no case-control studies available for this drug.

master protocol