Study |
Type of data |
Exposure measurement |
Outcome assessment |
Adjustment |
Källén (control exposed to ergots), 2011
|
population based cohort propective
|
Pregnant women who attend antenatal clinics in Sweden (which the vast majority do) are interviewed by a midwife and asked about drugs used since the pregnancy started. This interview is usually made before the end of the first trimester (usually between weeks 10 and 12 of pregnancy).
|
The outcomes were ascertained from multiple sources: the paediatric form of the Medical Birth Register, the Register of Birth Defects and the Patient Register.
|
No adjustment for this control group.
|
Källén (control unexposed, disease free), 2011
|
population based cohort propective
|
Pregnant women who attend antenatal clinics in Sweden (which the vast majority do) are interviewed by a midwife and asked about drugs used since the pregnancy started. This interview is usually made before the end of the first trimester (usually between weeks 10 and 12 of pregnancy).
|
The outcomes were ascertained from multiple sources: the paediatric form of the Medical Birth Register, the Register of Birth Defects and the Patient Register.
|
No adjustment for this group of exposure.
|
Nezvalová-Henriksen (Control unexposed, disease free), 2013
|
population based cohort retrospective
|
The Norwegian Prescription Database (NorPD) was the source of information on the individual triptan prescriptions. The timing of triptan redemption, in gestational weeks, was determined by the number of weeks from the onset of pregnancy to the date the prescription was redeemed.
|
The medical birth registry of Norway where data are collected via obligatory standardised forms by trained health personnel during medical check-ups during pregnancy and during the delivery and the subsequent hospital stay.
|
The confounding factors included, among others, maternal age, pregnancy complications, prescribed poten- tially teratogenic drugs during pregnancy, other co-medication during pregnancy, and for some outcomes delivery complications
|
Nezvalová-Henriksen (Control unexposed, sick), 2013
|
population based cohort retrospective
|
The Norwegian Prescription Database (NorPD) was the source of information on the individual triptan prescriptions. The timing of triptan redemption, in gestational weeks, was determined by the number of weeks from the onset of pregnancy to the date the prescription was redeemed.
|
The medical birth registry of Norway where data are collected via obligatory standardised forms by trained health personnel during medical check-ups during pregnancy and during the delivery and the subsequent hospital stay.
|
No adjustment for this control group.
|
Spielmann (Control mainly exposed other treatments, sick), 2017
|
prospective cohort
|
All data are recorded using structured questionnaires via phone interview and/or as a written form.
|
Structured questionnaire administered via phone interview and/or as a written form, notably on gestational age at birth, weight, length, head circumference, Apgar score, umbilical artery pH, birth defects, postnatal disorders, pregnancy loss. Medical reports requested in cases of birth defects.
|
No adjustment for this group of exposure.
|
Spielmann (Control unexposed, disease free), 2017
|
prospective cohort
|
All data are recorded using structured questionnaires via phone interview and/or as a written form.
|
Structured questionnaire administered via phone interview and/or as a written form, notably on gestational age at birth, weight, length, head circumference, Apgar score, umbilical artery pH, birth defects, postnatal disorders, pregnancy loss. Medical reports requested in cases of birth defects.
|
No adjustment for this group of exposure.
|