Objective:

pmc

0234361

3163

Contraception

0010-78241879-0518

40451566

12381897

10.1016/j.contraception.2025.110978

HHSPA2091717

Article

Progestin-only contraception and thrombosis: an updated systematic review

Tepper

Naomi K.

MD, MPHaNguyen

Antoinette T.

MD, MPHaWhiteman

Maura K.

PhDaCurtis

Kathryn M.

PhDa

aDivision of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, GA, USA

Corresponding author: Naomi Tepper: ntepper@cdc.gov

1382025

72026

3052025

2882025

159110978110978Objective:

Evidence is limited on whether use of progestin-only contraception (POC) is associated with risk of thrombosis. Our objective was to update an earlier systematic review on POC and thrombosis risk.

Methods:

We searched for articles that examined risk of venous thromboembolism (VTE) (e.g., deep venous thrombosis or pulmonary embolism) or arterial thromboembolism (ATE) (e.g., myocardial infarction or stroke) among women with thrombogenic conditions or characteristics or in the general population using POC, compared with women using non-hormonal or no contraception, published during February 1, 2016 – November 30, 2022. We also included articles from a previous systematic review with articles published through January 2016. We assessed quality for each study and certainty of evidence for all outcomes.

Results:

Thirty-three articles met inclusion criteria; one was good quality, 20 were fair quality, and 12 were poor quality. Seven articles were newly identified, and 26 were included in the previous review. Risk of VTE, but not ATE, was generally elevated with depot medroxyprogesterone acetate (DMPA) use among women with certain thrombogenic conditions or characteristics (e.g., diabetes or postpartum) and women in the general population. Risks of VTE and ATE were generally not elevated with use of other POC, including levonorgestrel intrauterine devices, implants, or progestin-only pills.

Conclusion:

Evidence suggests that risk of VTE, but not ATE, is increased with DMPA use compared with non-use among women with certain thrombogenic conditions and women in the general population. Evidence does not suggest increased risk of VTE or ATE with use of other POC. While several studies examined thrombosis risk with POC use and thrombogenic conditions or characteristics, data are limited for individual conditions or characteristics and no evidence was identified for most conditions. The certainty of evidence is low or very low for all outcomes.

contraceptionprogestin-only contraceptionthromboembolismsystematic review

1.Introduction

Although relatively rare among women of reproductive age, venous thromboembolism (VTE) (including deep venous thrombosis [DVT] and pulmonary embolism [PE]) and arterial thromboembolism (ATE) (including stroke and acute myocardial infarction [AMI]) can lead to significant morbidity [1–4]. The association between combined hormonal contraceptives (i.e., containing estrogen and progestin) and increased risk for thrombosis, both VTE and ATE, is well established [5, 6]. Emerging evidence has suggested that some progestin-only contraception (POC), specifically depot medroxyprogesterone acetate (DMPA) injectables, may also be associated with VTE [7]. Studies have generally not found an increased risk of VTE or ATE with use of other POC, i.e., levonorgestrel intrauterine devices (LNG-IUDs), progestin-only implants, and progestin-only pills (POPs) [8].

Certain characteristics (e.g., postpartum status) and medical conditions (e.g., thrombophilias, sickle cell disease, systemic lupus erythematosus, diabetes, and hypertension) confer an increased risk of thrombosis [9–11]. Women with these thrombogenic conditions are at additional increased risk for thrombosis and associated morbidity during pregnancy [12]. It is important that women with thrombogenic conditions are able to select and use contraceptive methods safely. However, there is theoretical concern that women with thrombogenic conditions might be at additional increased risk of thrombosis with use of certain hormonal contraceptives. Knowledge is limited on whether POC use might further elevate thrombosis risk in women with most thrombogenic conditions. The U.S. Centers for Disease Control and Prevention (CDC) publishes the U.S. Medical Eligibility Criteria for Contraceptive Use (US MEC) [13], which provides evidence-based guidance on the safety of contraceptive methods for patients with certain characteristics or medical conditions, including patients with thrombogenic conditions. As part of a process to update the US MEC, the objective of this systematic review was to evaluate the evidence on risk of thrombosis with POC use, among women with thrombogenic conditions or in the general population. This review updates a previous systematic review on POC and risk of thrombosis, which included studies published through January 2016 [8]. The previous review identified only 9 studies of women with thrombogenic conditions or characteristics, with generally only 1 or 2 studies per condition, thereby limiting conclusions that could be made about most thrombogenic conditions.

2.Methods

We conducted this systematic review according to the methods of a previously published systematic review on this topic [8]. The results are reported following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [14].

2.1.Eligibility criteria

Studies were eligible for inclusion if they examined thrombosis risk among women using POC. The population of interest was women with characteristics or medical conditions that confer an increased risk for VTE or ATE, e.g., postpartum, hypertension, or diabetes. We also included studies of women in the general population (those without thrombogenic conditions or not specified), to further examine thrombosis risk with use of POC. The exposure of interest was any POC, i.e., LNG-IUDs, progestin-only implants, progestin-only injectables (DMPA or norethisterone enanthate [NET-EN]), POPs, or emergency contraceptive pills. We also included articles examining progestin-only medications with unspecified or non-contraceptive formulations or used for therapeutic purposes, as the dose of progestin might have been higher than contraceptive dosing. The comparison was use of non-hormonal or no contraception. The outcomes of interest were VTE (DVT or PE) or ATE (stroke or AMI). We included randomized controlled trials (RCTs), non-randomized trials, cohort studies, and case-control studies. We excluded non-comparative studies, e.g., case series, case reports and review articles.

2.2.Literature search

We worked with a research librarian at the U.S. Centers for Disease Control and Prevention to develop the search strategy (Appendix A). The search was conducted in MEDLINE, Embase, Cochrane, CINAHL, Scopus, and ClinicalTrials.gov databases. The previous systematic review included articles published from database inception through January 31, 2016 [8]; therefore this updated search included articles published from February 1, 2016, through November 30, 2022. We considered articles in all languages. We did not consider abstracts from scientific conferences.

2.3.Study selection and data extraction

Among articles identified by the search strategy, all titles and abstracts were screened independently by at least two co-authors, using the Covidence platform [15]. Two co-authors then reviewed full-text articles to determine if they met inclusion criteria. Any conflicts were resolved by discussion. Standardized evidence tables were used to summarize information on each study.

2.4.Study quality assessment

Study quality was assessed in the previous review using the United States Preventive Services Task Force (USPSTF) system [16]. Therefore, we assessed the quality of each newly identified study using the USPSTF system. RCTs are level I evidence, non-randomized trials are level II-1 evidence, and cohort or case control studies are level II-2 evidence. Internal validity (risk of bias) of studies is considered based on criteria that are specific to the study design, such as participant selection, measurement of contraceptive use and outcomes, and assessment of confounding. Studies were assessed as being of good, fair, or poor quality. Two co-authors independently assessed study quality, and conflicts were resolved by discussion.

2.5.Data synthesis

We summarized descriptive statistics, unadjusted and adjusted point estimates, and results of significance tests. We did not conduct meta-analyses due to heterogeneity of study populations, exposures, and outcomes.

2.6.Certainty of evidence methods

We assessed the certainty of evidence using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) system [17–19]. For each outcome, we considered risk of bias, directness, precision, and consistency to be not serious, serious, or very serious. Based on these assessments, the certainty of evidence was rated as high, moderate, low, or very low. At baseline, RCTs are considered to have high certainty, and non-randomized trials and observational studies are considered to have low certainty; ratings are then adjusted based on the criteria previously listed. Outcomes related to use of unspecified or non-contraceptive progestins were not included in GRADE.

3.Results

We identified 1114 articles through our updated database search (February 2016 through November 2022), from which 50 articles were identified for full-text review (Figure 1). Among these articles, 43 were excluded (22 wrong study design, 12 wrong intervention, 5 wrong outcomes, 3 wrong comparison, and 1 abstract only). Seven newly identified articles met inclusion criteria [20–26]; one article [26] was written by the authors of this systematic review. Twenty-six articles are also included from the previous review [27–52], for a total of 33 included articles. These 33 articles represent 30 studies, as results from 3 studies were reported in more than one article [27, 29, 30, 38, 39, 46].

The articles all described cohort or case-control studies and reported on women using the following contraceptive methods (Table 1, Figures 2–4, Appendix B). Regarding LNG-IUDs there were 3 articles on women with thrombogenic conditions [23, 24, 30] and 7 articles on women in the general population [20, 30, 40–43, 51]. Regarding implants there were 3 articles on women with thrombogenic conditions [21, 23, 25] and 5 articles on women in the general population [20, 30, 40, 42, 45]. Regarding DMPA there were 6 articles on women with thrombogenic conditions [23, 25–27, 30, 44] and 4 articles on women in the general population [20, 27, 30, 51]). Regarding POPs there were 7 articles on women with thrombogenic conditions [23, 25, 27, 32, 34, 44, 50] and 15 articles on women in the general population [20, 22, 27, 30, 33, 34, 36–41, 43, 48, 49]. Regarding POC (e.g., methods combined, not specified, or non-contraceptive formulations) there were 5 articles on women with thrombogenic conditions [24, 25, 30, 31, 35] and 5 articles on women in the general population [20, 28, 29, 46, 52].

3.1.Study quality

All studies provided level II-2 evidence from cohort or case-control studies. Most studies were deemed to be of fair or poor quality, with the exception of 1 study that was deemed to be of good quality (Appendix B.1 and Appendix B.2) [34]. Eighteen studies (19 articles) [20–22, 24–27, 30, 33, 36–43, 45, 51] were deemed to be of fair quality because: there were different participation rates between groups [30, 33]; contraceptive types and/or thrombosis outcomes were obtained from diagnosis codes and were not confirmed by medical records [20–22, 25, 26, 36, 37, 40–43]; contraceptive types were obtained by patient self-report soon after outcome but were not verified by medical records [27, 38, 39, 45, 51]; or analyses did not account for age [24]. Thirteen studies [23, 28, 29, 31, 32, 35, 44, 46–50, 52] were deemed to be of poor quality because: source population was not described [44]; participation rates were not described [32, 44]; progestin formulation and dose were not specified [46]; contraception and/or outcome ascertainment and verification were not described [35, 44]; POC types were not separated in analyses [28, 29, 31, 35, 52]; statistical testing was not reported [23, 44, 47, 48]; or analyses did not account for any confounders [49, 50].

3.2.Women using LNG-IUDs3.2.1.Women with thrombogenic conditions or characteristics

Three studies examined LNG-IUD use among women with thrombogenic conditions, including history of VTE (2 studies [23, 24]) or factor V Leiden (FVL) mutation (1 study [30]) (Table 1, Figure 2, Appendix B.1). Two cohort studies of women with history of VTE found that incidence of VTE was lower with use of LNG-IUDs compared with non-use (5.3% in LNG-IUD users vs. 13.5% in non-users; 0% per year in LNG-IUD users vs. 4.7% per year in non-users) (statistical testing not reported) [23, 24]. One case-control study of women with FVL mutation found that odds of VTE were statistically significantly increased with LNG-IUD use compared with women without the mutation not using HC (odds ratio [OR] 3.2 [95% confidence interval (CI) 1.2–10.4]) [30].

3.2.2.Women in the general population

Seven studies examined LNG-IUD use among women in the general population, 4 cohort studies [40–43] and 3 case-control studies [20, 30, 51] (Table 1, Figure 4, Appendix B.2). None of the studies found statistically significantly increased risk estimates of VTE, stroke, or AMI with use of LNG-IUD compared with non-use (adjusted OR [aOR] and adjusted relative risk [aRR] or adjusted rate ratio range 0.3–1.0).

3.3.Women using implants3.3.1.Women with thrombogenic conditions or characteristics

Three cohort studies examined implant use among women with thrombogenic conditions or characteristics including: history of VTE, 1 study [23]; postpartum, 1 study [21]; and diabetes, 1 study [25] (Table 1, Figure 2, Appendix B.1). One study of women with history of VTE reported VTE incidence of 33.3% in etonogestrel implant users compared with 13.5% in non-users (statistical testing not reported) [23]. One study of postpartum women found that risk of VTE in etonogestrel implant users compared with non-users was not statistically significantly increased (aOR 1.8, 95% CI 0.4–7.5) [21]. One study of women with diabetes found no thrombotic events in etonogestrel implant users [25].

3.3.2.Women in the general population

Five studies examined implant use among women in the general population, consisting of 2 cohort studies [40, 42] and 3 case-control studies [20, 30, 45] (Table 1, Figure 4, Appendix B.2). Among the 3 studies that reported on VTE, none found statistically significantly increased risk of VTE with use of implants (etonogestrel or levonorgestrel) compared with non-use (aOR 0.9, 95% CI 0.5–1.6; aOR 1.1, 95% CI 0.7–1.8; and aRR 1.4, 95% CI 0.6–3.4) [20, 30, 42]. Among the 2 studies that reported on stroke, neither found statistically significantly increased risk estimates of stroke with use of implants (levonorgestrel or type unspecified) compared with non-use (aRR 0.9, 95% CI 0.3–2.7; and aOR 1.0, 95% CI 0.1–9.2) [40, 45]. Two studies found that risk of AMI with use of implants (levonorgestrel or type unspecified) compared with non-use was increased but not statistically significantly (aRR 2.1, 95% CI 0.7–6.7; and aOR 3.5, 95% CI 0.2–56.5) [40, 45].

3.4.Women using DMPA3.4.1.Women with thrombogenic conditions or characteristics

Six studies examined DMPA use among women with thrombogenic conditions or characteristics [23, 25–27, 30, 44], including: FVL mutation or history of VTE, 2 studies [23, 30]; postpartum, 1 study [26]; diabetes, 1 study [25]; smoking, 1 study [27]; and lupus, 1 study [44] (Table 1, Figure 2, Figure 3, Appendix B.1). One cohort study of women with a history of VTE found no recurrent VTEs in DMPA users and 5 (13.5%) recurrent VTEs in non-users [23]. One case-control study of women with FVL mutation found that risk of VTE with DMPA use compared with non-users without the mutation was significantly increased (OR 16.7, 95% CI 2.4–714) [30]. One cohort study of postpartum women found that risk of VTE in DMPA users compared with non-users was statistically significantly increased (incidence rate ratio [IRR] 1.9, 95% CI 1.4–2.7) [26]. One retrospective cohort study of women with diabetes found that risk of ATE or VTE (41% of outcomes were stroke, 26% AMI, 33% VTE) in DMPA users compared with IUD users (type not specified) was significantly increased (adjusted hazard ratio [aHR] 4.7, 95% CI 2.5–8.8) [25]. One case-control study of women who smoked found that odds of VTE in progestin-only injectables (mostly DMPA) compared with non-users who did not smoke was increased but not statistically significant (aOR 7.0, 95% CI 0.4–138) [27]. One cohort study of women with lupus found an incidence of AMI in women using NET-EN of 10% compared with 0% in non-users and an incidence of PE in women using NET-EN of 0% compared with 5.6% in non-users; no statistical testing was reported [44].

3.4.2.Women in the general population

Four case-control studies examined DMPA use among women in the general population [20, 27, 30, 51] (Table 1, Figure 4, Appendix B.2). Three studies found that odds of VTE with DMPA use compared with non-use were statistically significantly increased (aOR 2.2, 95% CI 1.3–4.0; aOR 2.4, 95% CI 2.0–2.9; and aOR 3.0, 95% CI 1.2–7.5) [20, 30, 51]. One study found that odds of VTE with use of injectables (mostly DMPA) compared with non-use were increased but not statistically significant (aOR 2.2, 95% CI 0.7–7.3) [27]. One study found that odds of ATE with use of injectables (mostly DMPA) compared with non-use were not increased (stroke aOR 0.9, 95% CI 0.5–1.5; AMI aOR 0.7, 95% CI 0.1–6.0) [27].

3.5.Women using POPs3.5.1.Women with thrombogenic conditions or characteristics

Seven studies examined POP use among women with thrombogenic conditions or characteristics [23, 25, 27, 32, 34, 44, 50], including: thrombophilia or history of VTE, 3 studies [23, 32, 50]; hypertension, 2 studies [27, 34]; diabetes, 1 study [25]; smoking, 2 studies [27, 34]; and lupus, 1 study [44] (Table 1, Figure 2, Figure 3, Appendix B.1). Three cohort studies of women with thrombophilia or history of VTE found that risk of VTE in POP users compared with non-users was not statistically significantly increased (aRR 0.8, 95% CI 0.2–3.9; HR 1.3, 95% CI 0.5–3.0; 1 [5.6%] in POP users vs. 5 [13.5%] in non-users) [23, 32, 50]. Two case-control studies of women with hypertension found that odds of VTE in POP users compared with non-users without hypertension were not statistically significantly increased (aOR 2.3, 95% CI 0.2–28.1; and aOR 1.2, 95% CI 0.1–23.7) [27, 34]. One of these studies found that odds of stroke in POP users with hypertension compared with non-users without hypertension were statistically significantly increased (aOR 10.9, 95% CI 3.6–33.8) [27], while the other study found no strokes among POP users with hypertension [34]. Both studies found that odds of AMI in POP users with hypertension compared with non-users without hypertension were not statistically significantly increased (aOR 0.8, 95% CI 0.03–20.4 [34]; and aOR 1.9, 95% CI 0.1–38.4 [27]). One retrospective cohort study of women with diabetes found that the risk of ATE or VTE (41% of outcomes were stroke, 26% AMI, 33% VTE) in POP users compared with IUD users (type not specified) was statistically significantly increased (aHR 3.69, 95% CI 2.10–6.48) [25]. Two case-control studies of women who smoked found that odds of VTE in POP users compared with non-users who did not smoke were not statistically significantly increased (aOR 0.95, 95% CI 0.2–6.0; and aOR 2.4, 95% CI 0.7–8.3) [27, 34]. One of these studies found that odds of stroke in POP users who smoked compared with non-users who did not smoke was not statistically significantly increased (aOR 2.5, 95% CI 0.5–13.2) [27]. The other study found a higher percentage of stroke in POP users (50%) than non-users (27%), although statistical testing was not reported [34]. Both studies found an increased odds of AMI in POP users who smoked compared with non-users who did not smoke, with odds statistically significant in one study (aOR 10.4, 95% CI 1.1–98.8) [34] but not in the other study (aOR 7.2, 95% CI 0.7–74.6) [27]. One cohort study of women with lupus found that the number of PEs was not higher in women using POPs (1 event [6.7%]) compared with non-use (1 event [5.6%]), but no statistical testing was done [44]. The same study found no AMIs in POP users [44].

3.5.2.Women in the general population

Fourteen studies (15 articles) examined POP use among women in the general population [20, 22, 27, 30, 33, 34, 36–41, 43, 48, 49]: 3 cohort [40, 41, 43] and 11 case-control studies (12 articles) [20, 22, 27, 30, 33, 34, 36–39, 48, 49] (Table 1, Figure 4, Appendix B.2). Among 9 studies that reported on VTE, none found that risk of VTE with use of POPs compared with non-use was statistically significantly increased (aRR, adjusted rate ratio, and aOR range 0.6–2.6) [20, 22, 27, 30, 34, 37, 38, 41, 43]. Among the 6 studies that reported on stroke, none found that risk of stroke with use of POPs compared with non-use was significantly increased (aRR and aOR range 0.4–1.6) [27, 34, 36, 39, 40, 49]. Among the 5 studies that reported on AMI, none found that risk of AMI with use of POPs compared with non-use was statistically significantly increased (aRR and aOR range 0.8–1.5) [27, 33, 34, 40, 48].

3.6.Women using POC (methods combined, not specified, or non-contraceptive formulations)3.6.1.Women with thrombogenic conditions or characteristics

Five studies examined POC use among women with thrombogenic conditions [24, 25, 30, 31, 35], including: thrombophilia or history of VTE, 4 studies [24, 30, 31, 35]; and diabetes, 1 study [25] (Table 1, Figure 2, Figure 3, Appendix B.1). Four of these were cohort studies [24, 25, 31, 35] and 1 was a case-control study [30]. Among 4 studies of women with thrombophilia or history of VTE, risk of VTE in POC users (not separated by type) compared with non-users with and without the condition was not statistically significantly increased (aOR and IRR range 0.6–3.6; incidence density 3.8% per year in POC users vs. 4.7% per year in non-users) [24, 30, 31, 35], with the exception of higher odds in women with FVL mutation using POC compared with non-users without the mutation (OR 5.4, 95% CI 2.5–13) [30]. One study of women with diabetes found that risk of ATE or VTE (41% of outcomes were stroke, 26% AMI, 33% VTE) in POC users compared with non-hormonal users was statistically significantly increased in women <35 years (aHR 2.02, 95% CI 1.51–2.70) but not in women >35 years (aHR 1.33, 95% CI 0.99–1.79) [25].

3.6.2.Women in the general population

Five case-control studies examined POC use broadly (methods combined, not specified, or non-contraceptive formulations) among women in the general population [20, 28, 29, 46, 52] (Table 1, Figure 2, Appendix B.2). Three studies found that odds of VTE with use of POC (methods combined or not specified) compared with non-use was not increased (aOR 1.2, 95% CI 0.4–3.6; aOR 1.0, 95% CI 0.6–1.6; and aOR 1.3, 95% CI 0.3–6.8) [28, 29, 52]. Three studies found that odds of VTE with use of non-contraceptive progestins (oral or type unspecified) for therapeutic reasons was statistically significantly increased compared with non-use (aOR range 2.0–5.9, 95% CI range 1.2–30.1) [20, 46, 52]. One of these studies did not find increased odds of stroke (aOR 1.1, 95% CI 0.2–7.1) or AMI (aOR 0.9, 95% CI 0.1–15.3) with use of oral therapeutic progestins compared with non-use [46].

3.7Certainty of evidence

Because all included studies were observational (cohort or case-control studies), the certainty of evidence for all outcomes was deemed to be low or very low [53]. For all outcomes, the risk of bias was considered to be serious or very serious due to concerns about selection bias (e.g., different participation rates between groups or rates were not reported), information bias (e.g., contraceptive type was not specified or confirmed, outcomes were not confirmed), lack of statistical testing, or concerns for confounding. For some outcomes, inconsistency was considered to be serious or very serious due to varying results between studies. For most outcomes, imprecision was considered to be serious or very serious due to wide CIs that included significantly decreased and significantly increased levels of risk. For some outcomes, indirectness was considered to be serious because analyses compared POC users with thrombogenic conditions to non-users without thrombogenic conditions (rather than non-users with thrombogenic conditions).

4.Discussion

This updated systematic review found that relative risk of thrombosis varied by POC type when compared with non-POC use. Risk of VTE was generally increased with DMPA use among women with certain thrombogenic conditions or characteristics, e.g., diabetes or postpartum, and women in the general population when compared with non-use; however, risk of ATE was not increased with DMPA use. Risks of VTE and ATE were generally not elevated with use of LNG-IUDs, implants, or POPs among women with certain thrombogenic conditions or women in the general population. Newly identified evidence was consistent with evidence included in the previously published systematic review [8].

The prior review included 3 studies on DMPA that found risk of VTE was statistically significantly increased [30, 51] or elevated to a similar degree but not statistically significant [27]. In this updated review, we identified 4 new studies on DMPA and risk for VTE, one among women with a history of VTE [23], one among postpartum women [26], one among women with diabetes [25], and one in the general population of DMPA users [20]. Three of these new studies also found increased relative risk for VTE [20, 25, 26]. One new study of DMPA use among women with history of VTE found a lower incidence of recurrent VTE in DMPA users than non-HC users, but no statistical testing was done [23]. An additional study found that risk of VTE was increased with use of DMPA compared with LNG-IUDs (age-adjusted IRR 3.7, 95% CI 1.3–10.4); although this study did not meet inclusion criteria for this review because the comparison group was LNG-IUD users, it lends support to the general body of evidence on DMPA [54].

Several meta-analyses have examined risk of thrombosis with POC use [7, 55–58]. In the most recent meta-analysis, risk of VTE was increased with use of DMPA compared with non-hormonal use (aOR 2.6, 95% CI 1.7–3.9) [7]. Risk of VTE was not statistically significantly increased with use of LNG-IUDs. Risk of VTE and ATE were not statistically significantly increased with use of POPs. Our systematic review differs from this meta-analysis because we separately describe studies on women with thrombogenic conditions and women in the general population. We also included several additional studies not included in the meta-analysis and studies published since the meta-analysis.

It is important to consider any increases in relative risk in the context of absolute risk. Although the relative risk of VTE may be increased 2–3 fold with use of DMPA, this represents a small increase in absolute numbers due to the rarity of VTE among women of reproductive age, at 5–10/10,000 women-years [4]. The absolute risk of stroke and MI are even lower among women of reproductive age: 19/100,000 women-years, and 10/100,000 women-years, respectively [40, 59]. Nonetheless, these outcomes might result in mortality or severe morbidity and incidence might be further increased in the setting of thrombogenic characteristics and medical conditions. The relative risk of VTE among postpartum women is 2.5–84 [60]. The relative risks of VTE in individuals with thrombophilias range from approximately 10 to 80 [61]. Approximately 25% of patients with sickle cell disease have a stroke by age 45 [62]. There is concern that use of certain hormonal contraceptives by women with thrombogenic conditions could further elevate their risk to a concerning level. Three of the studies that were identified in this review found that VTE risk was increased with use of DMPA compared with no use of DMPA among women who are postpartum or have diabetes [25, 26], and VTE was increased among DMPA users who smoke compared with non-users who do not smoke [27].

Reasons for the increased risk with DMPA may be related to the higher dose of progestin delivered or may be due to an interaction of DMPA and other thrombogenic changes. Three studies found an increased risk of VTE with progestins in non-contraceptive formulations or doses or used for non-contraceptive purposes (e.g., menstrual disorders) [20, 46, 52]; doses of progestin were likely higher than contraceptive doses. This finding suggests a potential dose response for thrombosis risk with POC that could explain some of the risk associated with DMPA, which is a relatively higher dose of progestin. In addition, DMPA has been found to have certain biological effects that may contribute to thrombogenesis. Several, mostly small, studies have found DMPA to be associated with increased total cholesterol, triglycerides, and low-density lipoprotein; decreased high-density lipoprotein; and reduced endothelial function [63–65]. DMPA does not appear to have deleterious effects on coagulation parameters [66–68]. However, the mechanism of thrombosis is complex and further study is needed to better understand impacts of DMPA on the hemostatic system and correlations with clinical outcomes.

In addition to further study of DMPA, future research on the drospirenone (DRSP) POP can provide additional evidence. No VTEs were reported in the Phase 3 clinical trials of the DRSP POP [69], however combined oral contraceptives (COCs) containing DRSP are associated with increased risk of VTE compared with COCs containing levonorgestrel [70]. Different progestins may have different effects on the coagulation system or may counteract the procoagulant effect of estrogen to varying degrees [71]. Additional study of DRSP POP use by women with thrombogenic conditions would advance understanding of any potential risks.

The body of evidence has several limitations. Most of the studies were deemed to be of fair or poor quality. The certainty of evidence was deemed to be low or very low for all outcomes, generally due to concerns about risk of bias and imprecision. A limited number of studies examined women with certain thrombogenic conditions or characteristics using POC, and most of these studies had relatively small numbers of women, limiting generalizability. Although the certainty of evidence was deemed to be low or very low, consistency across studies lends some confidence to the findings, e.g., increased risk with DMPA and lack of risk with POPs. Evidence remains limited on safety of these methods in women with most thrombogenic conditions and characteristics, with no studies for most conditions. Given that mechanisms of thrombosis differ between conditions, it is not possible to extrapolate evidence across different thrombogenic conditions and characteristics.

In conclusion, evidence suggests that risk of VTE is increased with use of DMPA compared with non-use. Evidence does not suggest an increased risk of VTE or ATE with use of other POC, including LNG-IUDs, implants, and POPs. Further study is needed on safety of POC use among women with thrombogenic conditions.

Supplementary Material

Acknowledgments

The authors would like to thank Joanna Taliano, MA, MLS, for helping to build the literature search strategy and running the searches.

Funding:

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Competing interests: The authors declare that they have no competing interests.

Disclaimer: The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

References[1]

Westhoff

, Yoon

, Tang

Risk Factors for Venous Thromboembolism Among Reproductive Age Women. J Womens Health 2016;25:63–70. doi: 10.1089/jwh.2015.5259.

[2]

Yonis

, Lokkegaard

, Kragholm

Stroke and myocardial infarction with contemporary hormonal contraception: real-world, nationwide, prospective cohort study. Brit Med J 2025;388:e082801. doi: 10.1136/bmj-2024-082801.

[3]

Yoon

, Bushnell

. Stroke in Women: A Review Focused on Epidemiology, Risk Factors, and Outcomes. J Stroke 2023;25:2–15. doi: 10.5853/jos.2022.03468.36746378

[4]

Heinemann

, Dinger

. Range of published estimates of venous thromboembolism incidence in young women. Contraception 2007;75:328–336. doi: 10.1016/j.contraception.2006.12.018.17434013

[5]

de Bastos

, Stegeman

, Rosendaal

Combined oral contraceptives: venous thrombosis. Cochrane Database Syst Rev 2014;2014:CD010813. doi: 10.1002/14651858.CD010813.pub2.

[6]

Roach

, Helmerhorst

, Lijfering

Combined oral contraceptives: the risk of myocardial infarction and ischemic stroke. Cochrane Database Syst Rev 2015;2015:CD011054. doi: 10.1002/14651858.CD011054.pub2.

[7]

Glisic

, Shahzad

, Tsoli

Association between progestin-only contraceptive use and cardiometabolic outcomes: A systematic review and meta-analysis. Eur J Prev Cardiol 2018;25:1042–1052. doi: 10.1177/2047487318774847.29745237

[8]

Tepper

, Whiteman

, Marchbanks

Progestin-only contraception and thromboembolism: A systematic review. Contraception 2016;94:678–700. doi: 10.1016/j.contraception.2016.04.014.27153743

[9]

Lijfering

, Rosendaal

, Cannegieter

. Risk factors for venous thrombosis - current understanding from an epidemiological point of view. Br J Haematol 2010;149:824–833. doi: 10.1111/j.1365-2141.2010.08206.x.20456358

[10]

Previtali

, Bucciarelli

, Passamonti

, Martinelli

. Risk factors for venous and arterial thrombosis. Blood Transfus 2011;9:120–138. doi: 10.2450/2010.0066-10.21084000

[11]

Curtis

, Tepper

, Jatlaoui

U.S. Medical Eligibility Criteria for Contraceptive Use, 2016. MMWR Recomm Rep 2016;65:1–103. doi: 10.15585/mmwr.rr6503a1.

[12]

Varrias

, Spanos

, Kokkinidis

Venous Thromboembolism in Pregnancy: Challenges and Solutions. Vasc Health Risk Manag 2023;19:469–484. doi: 10.2147/VHRM.S404537.37492280

[13]

Nguyen

, Curtis

, Tepper

U.S. Medical Eligibility Criteria for Contraceptive Use, 2024. MMWR Recomm Rep 2024;73:1–126. doi: 10.15585/mmwr.rr7304a1.

[14]

Page

, McKenzie

, Bossuyt

The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. Brit Med J 2021;372:n71. doi: 10.1136/bmj.n71.33782057

[15]

Veritas Health Innovation. Covidence systematic review software. https://www.covidence.org/ (accessed March 13, 2025).

[16]

Harris

, Helfand

, Woolf

Current methods of the US Preventive Services Task Force: a review of the process. Am J Prev Med 2001;20:21–35. doi: 10.1016/s0749-3797(01)00261–6.

[17]

GRADEpro Guideline Development Tool [Software]. 2022. Hamilton (ON): McMaster University (developed by Evidence Prime). https://www.gradepro.org/

[18]

Guyatt

, Oxman

, Akl

GRADE guidelines: 1. Introduction-GRADE evidence profiles and summary of findings tables. J Clin Epidemiol 2011;64:383–394. doi: 10.1016/j.jclinepi.2010.04.026.21195583

[19]

Guyatt

, Oxman

, Vist

GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. Brit Med J 2008;336:924–926. doi: 10.1136/bmj.39489.470347.AD.18436948

[20]

Cockrum

, Soo

, Ham

Association of Progestogens and Venous Thromboembolism Among Women of Reproductive Age. Obstet Gynecol 2022;140:477–487. doi: 10.1097/AOG.0000000000004896.35926206

[21]

Floyd

, Beasley

, Swaim

Association of Immediate Postpartum Etonogestrel Implant Insertion and Venous Thromboembolism. Obstet Gynecol 2020;135:1275–1280. doi: 10.1097/AOG.0000000000003760.32459418

[22]

Heikinheimo

, Toffol

, Partonen

Systemic hormonal contraception and risk of venous thromboembolism. Acta Obstet Gynecol Scand 2022;101:846–855. doi: 10.1111/aogs.14384.35633036

[23]

Maher

, Quint

, Weyand

. Management of Contraception in Adolescent Females With Hormone-Related Venous Thromboembolism. J Adolescent Health 2022;71:127–131. doi: 10.1016/j.jadohealth.2022.02.009.

[24]

Martinelli

, Lensing

, Middeldorp

Recurrent venous thromboembolism and abnormal uterine bleeding with anticoagulant and hormone therapy use. Blood 2016;127:1417–1425. doi: 10.1182/blood-2015-08-665927.26696010

[25]

O’Brien

, Koch

, Vesely

, Schwarz

. Hormonal Contraception and Risk of Thromboembolism in Women With Diabetes. Diabetes Care 2017;40:233–238. doi: 10.2337/dc16-1534.27899496

[26]

Tepper

, Jeng

, Curtis

Venous Thromboembolism Among Women Initiating Depot Medroxyprogesterone Acetate Immediately Postpartum. Obstet Gynecol 2019;133:533–540. doi: 10.1097/AOG.0000000000003135.30741807

[27]

Cardiovascular disease and use of oral and injectable progestogen-only contraceptives and combined injectable contraceptives. Results of an international, multicenter, case-control study. World Health Organization Collaborative Study of Cardiovascular Disease and Steroid Hormone Contraception. Contraception 1998; 57:315–324. PMID: 9673838.9673838

[28]

Barsoum

, Heit

, Ashrani

Is progestin an independent risk factor for incident venous thromboembolism? A population-based case-control study. Thromb Res 2010;126:373–378. doi: 10.1016/j.thromres.2010.08.010.20833412

[29]

Bergendal

, Bremme

, Hedenmalm

Risk factors for venous thromboembolism in pre-and postmenopausal women. Thromb Res 2012;130:596–601. doi: 10.1016/j.thromres.2012.05.024.22704078

[30]

Bergendal

, Persson

, Odeberg

Association of venous thromboembolism with hormonal contraception and thrombophilic genotypes. Obstet Gynecol 2014;124:600–609. doi: 10.1097/aog.0000000000000411.25162263

[31]

Christiansen

, Lijfering

, Helmerhorst

Sex difference in risk of recurrent venous thrombosis and the risk profile for a second event. J Thromb Haemost 2010;8:2159–2168. doi: 10.1111/j.1538-7836.2010.03994.x.20738758

[32]

Conard

, Plu-Bureau

, Bahi

Progestogen-only contraception in women at high risk of venous thromboembolism. Contraception 2004;70:437–441. doi: 10.1016/j.contraception.2004.07.009.15541404

[33]

Dunn

, Thorogood

, Faragher

Oral contraceptives and myocardial infarction: results of the MICA case-control study. Brit Med J 1999;318:1579–1583. doi: 10.1136/bmj.318.7198.1579.10364115

[34]

Heinemann

, Assmann

, DoMinh

, Garbe

. Oral progestogen-only contraceptives and cardiovascular risk: results from the Transnational Study on Oral Contraceptives and the Health of Young Women. Eur J Contracept Reprod Health Care 1999;4:67–73. doi: 10.3109/13625189909064007.10427481

[35]

Le Moigne

, Tromeur

, Delluc

Risk of recurrent venous thromboembolism on progestin-only contraception: a cohort study. Haematologica 2016;101:e12–14. doi: 10.3324/haematol.2015.134882.26452982

[36]

Lidegaard

Oral contraception and risk of a cerebral thromboembolic attack: results of a case-control study. Brit Med J 1993;306:956–963. doi: 10.1136/bmj.306.6883.956.8490470

[37]

Lidegaard

, Edstrom

, Kreiner

. Oral contraceptives and venous thromboembolism. A case-control study. Contraception 1998;57:291–301. doi: 10.1016/s0010-7824(98)00033-x.9673836

[38]

Lidegaard

, Edstrom

, Kreiner

. Oral contraceptives and venous thromboembolism: a five-year national case-control study. Contraception 2002;65:187–196. doi: 10.1016/s0010-7824(01)00307-9.11929640

[39]

Lidegaard

, Kreiner

. Contraceptives and cerebral thrombosis: a five-year national case-control study. Contraception 2002;65:197–205. doi: 10.1016/s0010-7824(01)00306-7.11929641

[40]

Lidegaard

, Lokkegaard

, Jensen

Thrombotic stroke and myocardial infarction with hormonal contraception. New Engl J Med 2012;366:2257–2266. doi: 10.1056/NEJMoa1111840.22693997

[41]

Lidegaard

, Lokkegaard

, Svendsen

, Agger

. Hormonal contraception and risk of venous thromboembolism: national follow-up study. Brit Med J 2009;339:b2890. doi: 10.1136/bmj.b2890.19679613

[42]

Lidegaard

, Nielsen

, Skovlund

, Lokkegaard

. Venous thrombosis in users of non-oral hormonal contraception: follow-up study, Denmark 2001–10. Brit Med J 2012;344:e2990. doi: 10.1136/bmj.e2990.22577198

[43]

Lidegaard

, Nielsen

, Skovlund

Risk of venous thromboembolism from use of oral contraceptives containing different progestogens and oestrogen doses: Danish cohort study, 2001–9. Brit Med J 2011;343:d6423. doi: 10.1136/bmj.d6423.22027398

[44]

Mintz

, Gutierrez

, Deleze

, Rodriguez

. Contraception with progestagens in systemic lupus erythematosus. Contraception 1984;30:29–38. doi: 10.1016/0010-7824(84)90076-3.6434228

[45]

Petitti

, Siscovick

, Sidney

Norplant implants and cardiovascular disease. Contraception 1998;57:361–362. doi: 10.1016/s0010-7824(98)00036–5.

[46]

Poulter

, Chang

, Farley

, Meirik

. Risk of cardiovascular diseases associated with oral progestagen preparations with therapeutic indications. Lancet 1999;354:1610. doi: 10.1016/s0140-6736(99)03132-3.

[47]

Rosenberg

, Palmer

, Rao

, Shapiro

. Low-dose oral contraceptive use and the risk of myocardial infarction. Arch Intern Med 2001;161:1065–1070. doi: 10.1001/archinte.161.8.1065.11322840

[48]

Thorogood

, Mann

, Murphy

, Vessey

. Is oral contraceptive use still associated with an increased risk of fatal myocardial infarction? Report of a case-control study. Br J Obstet Gynaecol 1991;98:1245–1253. doi: 10.1111/j.1471-0528.1991.tb15397.x.1777457

[49]

Tzourio

, Tehindrazanarivelo

, Iglesias

Case-control study of migraine and risk of ischaemic stroke in young women. Brit Med J 1995;310:830–833. doi: 10.1136/bmj.310.6983.830.7711619

[50]

Vaillant-Roussel

, Ouchchane

, Dauphin

Risk factors for recurrence of venous thromboembolism associated with the use of oral contraceptives. Contraception 2011;84:e23–30. doi: 10.1016/j.contraception.2011.06.008.22018134

[51]

van Hylckama Vlieg

, Helmerhorst

, Rosendaal

. The risk of deep venous thrombosis associated with injectable depot-medroxyprogesterone acetate contraceptives or a levonorgestrel intrauterine device. Arterioscl Throm Vas 2010;30:2297–2300. doi: 10.1161/atvbaha.110.211482.

[52]

Vasilakis

, Jick

, del Mar Melero-Montes

. Risk of idiopathic venous thromboembolism in users of progestagens alone. Lancet 1999;354:1610–1611. doi: 10.1016/s0140-6736(99)04394-9.

[53]

CDC. Supplementary Appendix. U.S. Medical Eligibility Criteria for Contraceptive Use, 2024 2024. Available from: https://stacks.cdc.gov/view/cdc/156516 (accessed March 13, 2025).

[54]

Kurvits

, Laius

, Uuskula

, Laanpere

. Trends in the use of hormonal contraception in Estonia 2005–2019 and the risk of arterial and venous thromboembolism: a population-based study. Eur J Contracept Reprod Health Care 2021;26:413–420. doi: 10.1080/13625187.2021.1931839.34160334

[55]

Bergendal

, Odlind

, Persson

, Kieler

. Limited knowledge on progestogen-only contraception and risk of venous thromboembolism. Acta Obstet Gynecol Scand 2009;88:261–266. doi: 10.1080/00016340902730375.19172422

[56]

Chakhtoura

, Canonico

, Gompel

Progestogen-only contraceptives and the risk of acute myocardial infarction: a meta-analysis. J Clin Endocrinol Metab 2011;96:1169–1174. doi: 10.1210/jc.2010-2065.21289250

[57]

Chakhtoura

, Canonico

, Gompel

Progestogen-only contraceptives and the risk of stroke: a meta-analysis. Stroke 2009;40:1059–1062. doi: 10.1161/STROKEAHA.108.538405.19211491

[58]

Mantha

, Karp

, Raghavan

Assessing the risk of venous thromboembolic events in women taking progestin-only contraception: a meta-analysis. Brit Med J 2012;345:e4944. doi: 10.1136/bmj.e4944.22872710

[59]

Ekker

, Verhoeven

, Vaartjes

Stroke incidence in young adults according to age, subtype, sex, and time trends. Neurology 2019;92:e2444–e2454. doi: 10.1212/WNL.0000000000007533.31019103

[60]

Jackson

, Curtis

, Gaffield

. Risk of venous thromboembolism during the postpartum period: a systematic review. Obstet Gynecol 2011;117:691–703. doi: 10.1097/AOG.0b013e31820ce2db.21343773

[61]

Mannucci

, Franchini

. Classic thrombophilic gene variants. Thromb Haemost 2015;114:885–889. doi: 10.1160/TH15-02-0141.26018405

[62]

Verduzco

, Nathan

. Sickle cell disease and stroke. Blood 2009;114:5117–5125. doi: 10.1182/blood-2009-05-220921.19797523

[63]

Williams

, MacDonald

. Influence of hormonal contraceptives on peripheral vascular function and structure in premenopausal females: a review. Am J Physiol Heart Circ Physiol 2021;320:H77–H89. doi: 10.1152/ajpheart.00614.2020.33164574

[64]

Turki

, Ayalew

, Mossie

, Mitiku

. Effects of hormonal contraceptives on lipid profile among women attending family planning unit in Goba Town Public Health Facilities, Bale, Southeast Ethiopia: a comparative cross-sectional study. Reprod Health 2023;20:185. doi: 10.1186/s12978-023-01727-4.38115027

[65]

Diab

, Zaki

. Contraception in diabetic women: comparative metabolic study of Norplant, depot medroxyprogesterone acetate, low dose oral contraceptive pill and CuT380A. J Obstet Gynaecol Res 2000;26:17–26. doi: 10.1111/j.1447-0756.2000.tb01195.x.10761326

[66]

Melhado-Kimura

, Bizzacchi

JMA

, Quaino

SKP

Effect of the injectable contraceptive depot-medroxyprogesterone acetate on coagulation parameters in new users. J Obstet Gynaecol Res 2017;43:1054–1060. doi: 10.1111/jog.13306.28503774

[67]

Kuhl

Effects of progestogens on haemostasis. Maturitas 1996;24:1–19. doi: 10.1016/0378-5122(96)00994-2.8794429

[68]

Goldstein

, Cushman

, Badger

, Johnson

. Effect of depomedroxyprogesterone acetate on coagulation parameter: a pilot study. Fertil Steril 2007;87:1267–1270. doi: 10.1016/j.fertnstert.2006.11.040.17336967

[69]

Palacios

, Colli

, Regidor

. Efficacy and cardiovascular safety of the new estrogen-free contraceptive pill containing 4 mg drospirenone alone in a 24/4 regime. BMC Womens Health 2020;20:218. doi: 10.1186/s12905-020-01080-9.33008401

[70]

Dragoman

, Tepper

, Fu

A systematic review and meta-analysis of venous thrombosis risk among users of combined oral contraception. Int J Gynaecol Obstet 2018;141:287–294. doi: 10.1002/ijgo.12455.29388678

[71]

Blanco-Molina

, Lozano

, Cano

Progestin-only contraception and venous thromboembolism. Thrombosis research 2012; 129:e257–262. doi:10.1016/j.thromres.2012.02.042.22425318

Figure 1.

PRISMA flow chart for updated search^a for evidence on progestin-only contraception and thrombosis

^a Updated search included articles published from February 1, 2016, through November 30, 2022. The previous systematic review included articles published from database inception through January 31, 2016 [8].

Figure 2.

Risk of venous thromboembolism among women with thrombogenic conditions using progestin-only contraception compared with non-use^a

DMPA, depot medroxyprogesterone acetate; POC, progestin-only contraception; POP, progestin-only pill; VTE, venous thromboembolism.

^a Reference group is use of non-hormonal or no contraception among women with the condition.

Figure 3.

Risk of venous thromboembolism among women with thrombogenic conditions using progestin-only contraception compared with non-users without thrombogenic conditions^a

DMPA, depot medroxyprogesterone acetate; FVL, factor V Leiden; IUD, intrauterine device; LNG, levonorgestrel; POC, progestin-only contraception; POP, progestin-only pill; PT, prothrombin.

^a Reference group is use of non-hormonal or no contraception among women without the condition.

Figure 4.

Risk of venous thromboembolism among women in the general population using progestin-only contraception^a

DMPA, depot medroxyprogesterone acetate; DSG, desogestrel; IUD, intrauterine device; LNG, levonorgestrel; NOR, norethisterone; POC, progestin-only contraception; POP, progestin-only pill.

^a Reference group for most studies is use of non-hormonal or no contraception.

Table 1.

Summary of evidence on progestin-only contraception and thrombosis

Study	Population	Contraception	Comparison group	Outcome	Risk of thrombosis (95% CI)
LNG-IUD use among women with thrombogenic conditions or characteristics
Maher, 2022 [23]	History VTE	LNG-IUD	+ history VTE, − HC	VTE	5.3% (LNG-IUD) vs 13.5% (non-use)
Martinelli, 2016 [24]	History VTE	LNG-IUD	+ history VTE, − HC	VTE	Incidence density/year: 0 (LNG-IUD) vs. 4.7% (non-use)
Bergendal, 2014 [30]	FVL	LNG-IUD	− FVL, − HC	VTE	OR 3.2 (1.2–10.4)
LNG-IUD use among women in general population
Lidegaard, 2009 [41]	General population	LNG-IUD	− HC	VTE	Adjusted rate ratio 0.9 (0.6–1.3)
Vlieg, 2010 [51]	General population	LNG-IUD	− HC	VTE	aOR 0.3 (0.1–1.3)
Lidegaard, 2011 [43]	General population	LNG-IUD	− HC	VTE	aRR 0.8 (0.6–1.1)
Lidegaard, 2012 [42]	General population	LNG-IUD	− HC	VTE	aRR 0.6 (0.4–0.8)
Bergendal, 2014 [30]	General population	LNG-IUD	− HC	VTE	aOR 0.6 (0.4–1.0)
Cockrum, 2022 [20]	General population	LNG-IUD	− HC	VTE	aOR 0.72 (0.50–1.05)
Lidegaard, 2012 [40]	General population	LNG-IUD	− HC	Stroke	aRR 0.7 (0.5–0.98)
Lidegaard, 2012 [40]	General population	LNG-IUD	− HC	AMI	aRR 1.0 (0.7–1.5)
Implant use among women with thrombogenic conditions or characteristics
Maher, 2022 [23]	History VTE	Implant (ETG)	+ history VTE, − HC	VTE	33.3% (implant) vs. 13.5% (non-use)
Floyd, 2020 [21]	Postpartum	Implant (ETG)	+ postpartum, − HC	VTE	aOR 1.81 (0.44–7.45)
O’Brien, 2017 [25]	Diabetes	Implant (ETG)	+ diabetes, + IUD (type unspecified)	VTE/A TE	0 (implant) vs 3.4/1000 WY (non-use)
Implant use among women in general population
Bergendal, 2014 [30]	General population	Medium dose (implants [ETG or LNG], oral DSG)	−HC	VTE	aOR 0.9 (0.5–1.6)
Cockrum, 2022 [20]	General population	Implant (ETG)	−HC	VTE	aOR 1.09 (0.66–1.82)
Lidegaard, 2012 [42]	General population	Implant (ETG)	−HC	VTE	aRR 1.4 (0.6–3.4)
Lidegaard, 2012 [40]	General population	Implant (type unspecified)	−HC	Stroke	aRR 0.9 (0.3–2.7)
Petitti, 1998 [45]	General population	Implant (LNG)	−HC	Stroke	aOR 1.0 (0.1–9.2)
Lidegaard, 2012 [40]	General population	Implant (type unspecified)	−HC	AMI	aRR 2.1 (0.7–6.7)
Petitti, 1998 [45]	General population	Implant (LNG)	−HC	AMI	aOR 3.5 (0.2–56.5)
DMPA use among women with thrombogenic conditions or characteristics
WHO, 1998 [27]	Smokers	Injectables (mostly DMPA)	− smoking, − HC	VTE	aOR 7.0 (0.4–138)
Maher, 2022 [23]	History of VTE	DMPA	+ history VTE, − HC	VTE	Incidence: 0% (DMPA) vs. 13.5% (non-use)
Bergendal, 2014 [30]	FVL	DMPA	− FVL, − HC	VTE	OR 16.7 (2.4–714)
Tepper, 2019 [26]	Postpartum	DMPA	+ postpartum, − HC	VTE	IRR 1.94 (1.38–2.72)
O’Brien, 2017 [25]	Diabetes	DMPA	+ diabetes, − HC	VTE or ATE	aHR 4.69 (2.51–8.77)
Mintz, 1984 [44]	Lupus	DMPA	+ lupus, − HC	PE	0% (DMPA) vs. 5.6% (non-use)
Mintz, 1984 [44]	Lupus	DMPA	+ lupus, − HC	AMI	10% (DMPA) vs. 0% (non-use)
DMPA use among women in general population
WHO, 1998 [27]	General population	Injectables (mostly DMPA)	− HC	VTE	aOR 2.2 (0.7–7.3)
Vlieg, 2010 [51]	General population	DMPA	− HC	VTE	aOR 3.0 (1.2–7.5)
Bergendal, 2014 [30]	General population	DMPA	− HC	VTE	aOR 2.2 (1.3–4.0)
Cockrum, 2022 [20]	General population	DMPA	− HC	VTE	aOR 2.37 (1.95–2.88)
WHO, 1998 [27]	General population	Injectables (mostly DMPA)	− HC	Stroke	aOR 0.9 (0.5–1.5)
WHO, 1998 [27]	General population	Injectables (mostly DMPA)	− HC	AMI	aOR 0.7 (0.1–6.0)
POP use among women with thrombogenic conditions or characteristics
Conard, 2004 [32]	Thrombophilia or history VTE	POP	+ thrombophilia or history VTE, − HC	VTE	aRR 0.8 (0.2–3.9)
Maher, 2022 [23]	History VTE	POP	+ history VTE, − HC	VTE	5.6% (POP) vs. 13.5% (non-use)
Vaillant-Roussel, 2011 [50]	History VTE	POP	+ history VTE, − HC	VTE	HR 1.3 (0.5–3.0)
Heinemann, 1999 [34]	Hypertension	POP	− HTN, − HC	VTE	aOR 2.3 (0.2–28.1)
WHO 1998 [27]	Hypertension	POP	− HTN, − HC	VTE	aOR 1.2 (0.1–23.7)
Heinemann, 1999 [34]	Smokers	POP	− smoking, − HC	VTE	aOR 0.95 (0.2–6.0)
WHO, 1998 [27]	Smokers	POP	− smoking, − HC	VTE	aOR 2.4 (0.7–8.3)
O’Brien, 2017 [25]	Diabetes	POP	+ diabetes, + IUD (type unspecified)	VTE/A TE	aHR 3.69 (2.10–6.48)
Mintz, 1984 [44]	Lupus	POP (LNG)	+ lupus, − HC	PE	6.7% (POP) vs. 5.6% (non-use)
Heinemann, 1999 [34]	Hypertension	POP	− HTN, − HC	Stroke	No strokes in POP users
WHO 1998 [27]	Hypertension	POP	− HTN, − HC	Stroke	aOR 10.9 (3.6–33.8)
Heinemann, 1999 [34]	Smokers	POP	− smoking, − HC	Stroke	50% (POP) vs. 27% (non-use)
WHO, 1998 [27]	Smokers	POP	− smoking, − HC	Stroke	aOR 2.5 (0.5–13.2)
Heinemann, 1999 [34]	Hypertension	POP	− HTN, − HC	AMI	aOR 0.8 (0.03–20.4)
WHO 1998 [27]	Hypertension	POP	− HTN, − HC	AMI	aOR 1.9 (0.1–38.4)
Heinemann, 1999 [34]	Smokers	POP	− smoking, − HC	AMI	aOR 10.4 (1.1–98.8)
WHO, 1998 [27]	Smokers	POP	− smoking, − HC	AMI	aOR 7.2 (0.7–74.6)
Rosenberg, 2001 [47]	Smokers	POP	+ smokers, − HC	AMI	50% (POP) vs. 17.9% (non-use)
Mintz, 1984 [44]	Lupus	POP (LNG)	+ lupus, − HC	AMI	0 vs 0
POP use among women in general population
Lidegaard, 1998 [37]	General population	POP	−HC	VTE	aOR 2.6 (0.7–9.8)
WHO, 1998 [27]	General population	POP	−HC	VTE	aOR 1.8 (0.8–4.2)
Lidegaard, 2002 [38]	General population	POP	−HC	VTE	aOR 2.0 (0.8–5.1)
Lidegaard, 2009 [41]	General population	POP (LNG or norethisterone)	−HC	VTE	Adjusted rate ratio 0.6 (0.3–1.04)
Lidegaard, 2009 [41]	General population	POP (DSG)	−HC	VTE	Adjusted rate ratio 1.1 (0.4–3.4)
Lidegaard, 2011 [43]	General population	POP (norethisterone)	−HC	VTE	aRR 0.6 (0.3–1.1)
Lidegaard, 2011 [43]	General population	POP (DSG)	−HC	VTE	aRR 0.6 (0.3–1.4)
Heinemann, 1999 [34]	General population	POP	−HC	VTE	aOR 0.7 (0.3–1.7)
Bergendal, 2014 [30]	General population	POP	−HC	VTE	aOR 0.8 (0.4–1.9)
Cockrum, 2022 [20]	General population	POP (norethindrone)	−HC	VTE	aOR 0.57 (0.43–0.76)
Heikinheimo, 2022 [22]	General population	POP	−HC	VTE	aOR 0.90 (0.68–1.18)
Lidegaard, 1993 [36]	General population	POP	−HC	Stroke	aOR 0.9 (0.4–2.4)
Tzourio, 1995 [49]	General population	POP	−HC	Stroke	OR 1
WHO, 1998 [27]	General population	POP	−HC	Stroke	aOR 1.1 (0.6–1.9)
Lidegaard, 2002 [39]	General population	POP	−HC	Stroke	aOR 1.0 (0.3–3.0)
Lidegaard, 2012 [40]	General population	POP (norethindrone)	−HC	Stroke	aRR 1.4 (0.9–2.0)
Lidegaard, 2012 [40]	General population	POP (LNG)	−HC	Stroke	aRR 0.4 (0.1–3.1)
Lidegaard, 2012 [40]	General population	POP (DSG)	−HC	Stroke	aRR 1.4 (0.7–2.6)
Heinemann, 1999 [34]	General population	POP	−HC	Stroke	aOR 1.6 (0.2–10.7)
Thorogood, 1991 [48]	General population	POP	−HC	AMI	20% (POP) vs. 31.6% (non-use)
WHO, 1998 [27]	General population	POP	−HC	AMI	aOR 0.98 (0.2–6.0)
Dunn, 1999 [33]	General population	POP	−HC	AMI	aOR 1.5 (0.6–3.7)
Lidegaard, 2012 [40]	General population	POP (norethindrone)	−HC	AMI	aRR 0.8 (0.4–1.6)
Lidegaard, 2012 [40]	General population	POP (LNG)	−HC	AMI	Incidence rate/100,000 WY: 0 (POP) vs. 13.2 (non-use)
Lidegaard, 2012 [40]	General population	POP (DSG)	−HC	AMI	aRR 1.5 (0.6–3.9)
Heinemann, 1999 [34]	General population	POP	−HC	AMI	aOR 0.9 (0.3–2.9)
POC (combined, unspecified, or non-contraceptive formulations) use among women with thrombogenic conditions or characteristics
Bergendal 2014 [30]	FVL mutation	POP, DMPA, implant, LNG-IUD	− FVL, − HC	VTE	aOR 5.4 (2.5–13)
Bergendal 2014 [30]	PT gene mutation	POP, DMPA, implant, LNG-IUD	− PT, − HC	VTE	aOR 0.7 (0.2–2.2)
Christiansen, 2010 [31]	History VTE	POP, DMPA	+history VTE, − HC	VTE	IRR 3.6 (0.7–17.3)
Le Moigne, 2016 [35]	History VTE	POP, implant, LNG-IUD	+history VTE, − HC	VTE	IRR 0.6 (0.3–1.5)
Martinelli, 2016 [24]	History VTE	POC	+history VTE, − HC	VTE	Incidence density/year: 3.8% (POC) vs. 4.7% (non-use)
O’Brien, 2017 [25]	Diabetes age <35	POC	+ diabetes, − HC	VTE/ATE	aHR 2.02 (1.51–2.70)
O’Brien, 2017 [25]	Diabetes age >35	POC	+ diabetes, − HC	VTE/A TE	aHR 1.33 (0.99–1.79)
POC (combined, unspecified, or non-contraceptive formulations) use among women in general population
Barsoum, 2010 [28]	General population	POC	−HC	VTE	aOR 1.2 (0.4–3.6)
Bergendal, 2012 [29]	General population	DMPA, implant, LNG-IUD	−HC	VTE	aOR 0.98 (0.6–1.6)
Cockrum, 2022 [20]	General population	Oral progesterone	−HC	VTE	aOR 1.07 (0.75–1.54)
Cockrum, 2022 [20]	General population	Oral MPA	−HC	VTE	aOR 1.98 (1.41–2.80)
Cockrum, 2022 [20]	General population	POP (norethindrone acetate)	−HC	VTE	aOR 3.00 (1.96–4.59)
Vasilakis, 1999 [52]	General population	POC (for contraception)	−HC	VTE	aOR 1.3 (0.3–6.8)
Vasilakis, 1999 [52]	General population	POC (for menstrual disorders)	−HC	VTE	aOR 5.3 (1.5–18.7)
Poulter, 1999 [46]	General population	POC (therapeutic reasons)	−HC	VTE	aOR 5.9 (1.2–30.1)
Poulter, 1999 [46]	General population	POC (therapeutic reasons)	−HC	Stroke	aOR 1.1 (0.2–7.1)
Poulter, 1999 [46]	General population	POC (therapeutic reasons)	−HC	AMI	aOR 0.9 (0.1–15.3)

+, with condition; - without condition; aHR, adjusted hazard ratio; AMI, acute myocardial infarction; aOR, adjusted odds ratio; aRR, adjusted relative risk; ATE, arterial thromboembolism; DMPA, depot medroxyprogesterone acetate; DSG, desogestrel; ETG, etonogestrel; FVL, factor V Leiden; HC, hormonal contraception; HTN, hypertension; IRR, incidence rate ratio; IUD, intrauterine device; LNG, levonorgestrel; MPA, medroxyprogesterone acetate; PE, pulmonary embolism; POC; progestin-only contraception; POP, progestin-only pills; PT, prothrombin; VTE, venous thromboembolism; WY, women-years.

Implications

Use of DMPA might increase risk of VTE among women with medical conditions associated with thrombosis and among women in the general population. Evidence does not suggest an increased risk of thrombosis with other POC. Further study is needed on safety of POC use by women with thrombogenic conditions.