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. 2025 Feb 12:388:e082801.
doi: 10.1136/bmj-2024-082801.

Stroke and myocardial infarction with contemporary hormonal contraception: real-world, nationwide, prospective cohort study

Affiliations

Stroke and myocardial infarction with contemporary hormonal contraception: real-world, nationwide, prospective cohort study

Harman Yonis et al. BMJ. .

Abstract

Objective: To evaluate the association between contemporary hormonal contraceptive use and the risk of incident ischaemic stroke and myocardial infarction.

Design: Real-world, nationwide, prospective cohort study.

Setting: Denmark, by use of national registries.

Participants: All women aged 15-49 years residing in Denmark between 1996 and 2021, with no history of arterial or venous thrombosis, antipsychotics use, cancer, thrombophilia, liver disease, kidney disease, polycystic ovary syndrome, endometriosis, infertility treatment, hormone therapy use, oophorectomy, and hysterectomy.

Main outcome measures: First time diagnosis of ischaemic stroke or myocardial infarction at discharge.

Results: Among 2 025 691 women followed up for 22 209 697 person years, 4730 ischaemic strokes and 2072 myocardial infarctions occurred. Standardised ischaemic stroke rate per 100 000 person years were 18 (95% confidence interval 18 to 19) for no use, 39 (36 to 42) for combined oral contraception, 33 (25 to 44) for progestin-only pills, and 23 (17 to 29) for intrauterine device. Standardised myocardial infarction rate per 100 000 person years were 8 (8 to 9) for no use, 18 (16 to 20) for combined oral contraception, 13 (8 to 19) for progestin-only pills, and 11 (7 to 16) for intrauterine device. Compared with no use, current use of combined oral contraception was associated with an adjusted rate ratio of 2.0 (1.9 to 2.2) for ischaemic stroke and 2.0 (1.7 to 2.2) for myocardial infarction. These corresponded to standardised rate differences of 21 (18 to 24) extra ischaemic strokes and 10 (7 to 12) extra myocardial infarctions per 100 000 person years. Compared with no use, current use of progestin-only pills was associated with an adjusted rate ratio of 1.6 (95% CI 1.3 to 2.0) for ischaemic stroke and 1.5 (1.1 to 2.1) for myocardial infarction, equating to 15 (6 to 24) extra ischaemic strokes and four (-1 to 9) extra myocardial infarctions per 100 000 person years. Increased arterial thrombotic risk was also observed with use of the combined vaginal ring (adjusted incidence rate ratio of 2.4 (1.5 to 3.7) for ischaemic stroke and 3.8 (2.0 to 7.3) for myocardial infarction), patch (3.4 (1.3 to 9.1) and no myocardial infarctions), and progestin-only implant (2.1 (1.2 to 3.8) and ≤3 myocardial infarctions), whereas no increased risk was observed with progestin-only intrauterine device (1.1 (1.0 to 1.3) for ischaemic stroke and 1.1 (0.9 to 1.3) for myocardial infarction).

Conclusions: Use of contemporary oestrogen-progestin and progestin-only contraceptives was associated with an increased risk of ischaemic stroke and, in some cases, myocardial infarction except for the levonorgestrel-releasing intrauterine device, which was not associated with either. Although absolute risks were low, clinicians should include the potential risk of arterial thrombosis in their assessment of the benefits and risks when prescribing a hormonal contraceptive method.

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Conflict of interest statement

Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/disclosure-of-interest/ and declare: AM, ALM, and LSM have received support from Sygeforsikringen “Danmark”; no support from any organisation for the submitted work; HY reports having received research grants from the Laerdal Foundation and TrygFonden, not relevant for this study. AM reports having received a research grant from the Danish Cancer Institute, not relevant for this study. EL reports travel support/meeting fees from Radiometer, Gedion Richter, Pfizer, Merck, and Astella Pharma. CT-P has received grants from Novo Nordisk and Bayer outside of the current study. CBG reported receiving personal fees and grants from Boehringer Ingelheim, Bristol Myers Squibb, Daiichi Sankyo, Pfizer, Janssen, Bayer, AbbVie, Abiomed, Alnylam, Cardionomic, CeleCor Therapeutics, HingRui, Medscape, Medtronic, Merck, Novo Nordisk, Novartis, PLX Pharma, REATA, NephroSynergy, and Boston Scientific, not relevant for this study. All other authors declare no financial competing interests.

Figures

Fig 1
Fig 1
Flowchart for study inclusion. *Use of hormonal contraceptives withdrawn from the market in Denmark before 2010 was censored, since data on these products already have been published in 2012 without the possibility of this study adding new information about the products. They include combined oral contraceptives containing 50 μg ethinyl oestradiol, 30-40 μg pills containing the progestin norethisterone, and the levonorgestrel-only oral contraceptive
Fig 2
Fig 2
Adjusted incidence rate ratio of ischaemic stroke and myocardial infarction with use of oral contraceptives according to type and duration of use with non-use as the reference. Adjusted for age, calendar-time, education, hypertension, diabetes, hypercholesterolaemia, and atrial fibrillation and flutter

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