Ciprofloxacin exposure and adverse pregnancy outcomes: A Danish nationwide cohort study

Objective To examine the association between maternal exposure to ciprofloxacin and the risk of miscarriage and major malformations. Design A nationwide register‐based cohort study. Setting Data were obtained from the Medical Birth Registry, the National Hospital Registry, the Danish National Prescr...

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Veröffentlicht in:BJOG : an international journal of obstetrics and gynaecology 2022-08, Vol.129 (9), p.1503-1511
Hauptverfasser: Noergaard, Mia, Gotfredsen, Ditte Resendal, Sørensen, Anne Mette Skov, Andersen, Jon Trærup
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container_end_page 1511
container_issue 9
container_start_page 1503
container_title BJOG : an international journal of obstetrics and gynaecology
container_volume 129
creator Noergaard, Mia
Gotfredsen, Ditte Resendal
Sørensen, Anne Mette Skov
Andersen, Jon Trærup
description Objective To examine the association between maternal exposure to ciprofloxacin and the risk of miscarriage and major malformations. Design A nationwide register‐based cohort study. Setting Data were obtained from the Medical Birth Registry, the National Hospital Registry, the Danish National Prescription Registry and Statistics Denmark. Population Data were collected in the period between 1997 and 2016 and included all registered pregnancies that ended in an elective termination, miscarriage, stillbirth or a live birth. Exposure was defined as redeeming one or more prescriptions of ciprofloxacin. Methods Miscarriage was defined as a diagnosis given before 22 weeks without any medical intervention. Major malformations were classified according to EUROCAT 1.4. We matched ciprofloxacin‐exposed pregnancies to unexposed pregnancies on the propensity score in a ratio 1:4. To estimate the hazard ratio (HR) of miscarriage a Cox proportional hazard regression model was used. A log binomial model was used to estimate the relative risk ratio (RR) of major malformations. Main outcome measures HR of miscarriage and the RR of major malformations. Results A total of 1 650 649 pregnancies were identified. Of these, 10 250 (2050 ciprofloxacin‐exposed) and 6100 (1220 ciprofloxacin‐exposed) were included in the miscarriage and major malformation analysis, respectively. The HR of miscarriage was 0.99 (95% confidence interval [CI] 0.84–1.17). For major malformation, the RR was 1.01 (95% CI 0.72–1.40). For the organ‐specific major malformations and the sensitivity analyses, no significant increased risks were identified. Conclusion We demonstrated no association between miscarriage and maternal ciprofloxacin exposure within the first 22 weeks of pregnancy, or between major malformations and maternal exposure during the first trimester. Tweetable No association between maternal ciprofloxacin exposure and adverse pregnancy outcomes. Tweetable No association between maternal ciprofloxacin exposure and adverse pregnancy outcomes.
doi_str_mv 10.1111/1471-0528.17083
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Design A nationwide register‐based cohort study. Setting Data were obtained from the Medical Birth Registry, the National Hospital Registry, the Danish National Prescription Registry and Statistics Denmark. Population Data were collected in the period between 1997 and 2016 and included all registered pregnancies that ended in an elective termination, miscarriage, stillbirth or a live birth. Exposure was defined as redeeming one or more prescriptions of ciprofloxacin. Methods Miscarriage was defined as a diagnosis given before 22 weeks without any medical intervention. Major malformations were classified according to EUROCAT 1.4. We matched ciprofloxacin‐exposed pregnancies to unexposed pregnancies on the propensity score in a ratio 1:4. To estimate the hazard ratio (HR) of miscarriage a Cox proportional hazard regression model was used. A log binomial model was used to estimate the relative risk ratio (RR) of major malformations. Main outcome measures HR of miscarriage and the RR of major malformations. Results A total of 1 650 649 pregnancies were identified. Of these, 10 250 (2050 ciprofloxacin‐exposed) and 6100 (1220 ciprofloxacin‐exposed) were included in the miscarriage and major malformation analysis, respectively. The HR of miscarriage was 0.99 (95% confidence interval [CI] 0.84–1.17). For major malformation, the RR was 1.01 (95% CI 0.72–1.40). For the organ‐specific major malformations and the sensitivity analyses, no significant increased risks were identified. Conclusion We demonstrated no association between miscarriage and maternal ciprofloxacin exposure within the first 22 weeks of pregnancy, or between major malformations and maternal exposure during the first trimester. Tweetable No association between maternal ciprofloxacin exposure and adverse pregnancy outcomes. Tweetable No association between maternal ciprofloxacin exposure and adverse pregnancy outcomes.</description><identifier>ISSN: 1470-0328</identifier><identifier>ISSN: 1471-0528</identifier><identifier>EISSN: 1471-0528</identifier><identifier>DOI: 10.1111/1471-0528.17083</identifier><identifier>PMID: 34954900</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Abortion ; Abortion, Spontaneous - chemically induced ; Abortion, Spontaneous - epidemiology ; Antibiotics ; Birth defects ; Ciprofloxacin ; Ciprofloxacin - adverse effects ; Clinical outcomes ; Cohort analysis ; Cohort Studies ; Denmark - epidemiology ; early exposure ; Female ; Fetuses ; Human exposure ; Humans ; major malformation ; Miscarriage ; Pregnancy ; Pregnancy Trimester, First ; Sensitivity analysis ; Statistical analysis ; Stillbirth</subject><ispartof>BJOG : an international journal of obstetrics and gynaecology, 2022-08, Vol.129 (9), p.1503-1511</ispartof><rights>2021 The Authors. 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Design A nationwide register‐based cohort study. Setting Data were obtained from the Medical Birth Registry, the National Hospital Registry, the Danish National Prescription Registry and Statistics Denmark. Population Data were collected in the period between 1997 and 2016 and included all registered pregnancies that ended in an elective termination, miscarriage, stillbirth or a live birth. Exposure was defined as redeeming one or more prescriptions of ciprofloxacin. Methods Miscarriage was defined as a diagnosis given before 22 weeks without any medical intervention. Major malformations were classified according to EUROCAT 1.4. We matched ciprofloxacin‐exposed pregnancies to unexposed pregnancies on the propensity score in a ratio 1:4. To estimate the hazard ratio (HR) of miscarriage a Cox proportional hazard regression model was used. A log binomial model was used to estimate the relative risk ratio (RR) of major malformations. Main outcome measures HR of miscarriage and the RR of major malformations. Results A total of 1 650 649 pregnancies were identified. Of these, 10 250 (2050 ciprofloxacin‐exposed) and 6100 (1220 ciprofloxacin‐exposed) were included in the miscarriage and major malformation analysis, respectively. The HR of miscarriage was 0.99 (95% confidence interval [CI] 0.84–1.17). For major malformation, the RR was 1.01 (95% CI 0.72–1.40). For the organ‐specific major malformations and the sensitivity analyses, no significant increased risks were identified. Conclusion We demonstrated no association between miscarriage and maternal ciprofloxacin exposure within the first 22 weeks of pregnancy, or between major malformations and maternal exposure during the first trimester. Tweetable No association between maternal ciprofloxacin exposure and adverse pregnancy outcomes. 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Gotfredsen, Ditte Resendal ; Sørensen, Anne Mette Skov ; Andersen, Jon Trærup</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4123-56bcf3fed38a9da2cdaebdc694d97abcf286a0b1af7b5040138a3d29cfb7a0413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Abortion</topic><topic>Abortion, Spontaneous - chemically induced</topic><topic>Abortion, Spontaneous - epidemiology</topic><topic>Antibiotics</topic><topic>Birth defects</topic><topic>Ciprofloxacin</topic><topic>Ciprofloxacin - adverse effects</topic><topic>Clinical outcomes</topic><topic>Cohort analysis</topic><topic>Cohort Studies</topic><topic>Denmark - epidemiology</topic><topic>early exposure</topic><topic>Female</topic><topic>Fetuses</topic><topic>Human exposure</topic><topic>Humans</topic><topic>major malformation</topic><topic>Miscarriage</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, First</topic><topic>Sensitivity analysis</topic><topic>Statistical analysis</topic><topic>Stillbirth</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Noergaard, Mia</creatorcontrib><creatorcontrib>Gotfredsen, Ditte Resendal</creatorcontrib><creatorcontrib>Sørensen, Anne Mette Skov</creatorcontrib><creatorcontrib>Andersen, Jon Trærup</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; 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Design A nationwide register‐based cohort study. Setting Data were obtained from the Medical Birth Registry, the National Hospital Registry, the Danish National Prescription Registry and Statistics Denmark. Population Data were collected in the period between 1997 and 2016 and included all registered pregnancies that ended in an elective termination, miscarriage, stillbirth or a live birth. Exposure was defined as redeeming one or more prescriptions of ciprofloxacin. Methods Miscarriage was defined as a diagnosis given before 22 weeks without any medical intervention. Major malformations were classified according to EUROCAT 1.4. We matched ciprofloxacin‐exposed pregnancies to unexposed pregnancies on the propensity score in a ratio 1:4. To estimate the hazard ratio (HR) of miscarriage a Cox proportional hazard regression model was used. A log binomial model was used to estimate the relative risk ratio (RR) of major malformations. Main outcome measures HR of miscarriage and the RR of major malformations. Results A total of 1 650 649 pregnancies were identified. Of these, 10 250 (2050 ciprofloxacin‐exposed) and 6100 (1220 ciprofloxacin‐exposed) were included in the miscarriage and major malformation analysis, respectively. The HR of miscarriage was 0.99 (95% confidence interval [CI] 0.84–1.17). For major malformation, the RR was 1.01 (95% CI 0.72–1.40). For the organ‐specific major malformations and the sensitivity analyses, no significant increased risks were identified. Conclusion We demonstrated no association between miscarriage and maternal ciprofloxacin exposure within the first 22 weeks of pregnancy, or between major malformations and maternal exposure during the first trimester. Tweetable No association between maternal ciprofloxacin exposure and adverse pregnancy outcomes. 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subjects Abortion
Abortion, Spontaneous - chemically induced
Abortion, Spontaneous - epidemiology
Antibiotics
Birth defects
Ciprofloxacin
Ciprofloxacin - adverse effects
Clinical outcomes
Cohort analysis
Cohort Studies
Denmark - epidemiology
early exposure
Female
Fetuses
Human exposure
Humans
major malformation
Miscarriage
Pregnancy
Pregnancy Trimester, First
Sensitivity analysis
Statistical analysis
Stillbirth
title Ciprofloxacin exposure and adverse pregnancy outcomes: A Danish nationwide cohort study
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