Mitchell D. Creinin , Jean Michel Foidart , Kristina Gemzell-Danielsson , Nina C. Flerin , Ali Kubba , Ulysse Gaspard , Jonathan Douxfils
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We compared adverse event rates in participants with and without cardiovascular risk factors and assessed discontinuation rates for cardiovascular adverse events.</div></div><div><h3>Results</h3><div>Of 3417 participants, 1410 (41.3%) had one or more, and 309 (9.0%) had two or more cardiovascular risk factors. We found no difference in discontinuation for any adverse events in participants with and without cardiovascular risk factors. Six (0.18%) participants discontinued for a cardiovascular complaint including four with risk factors: three (0.09%) due to hypertension (all had baseline BP ≥130/85 mmHg and one or more additional risk factors) and one due to venous thrombosis (BP ≥130/85 mmHg). Of 375 participants with baseline BP ≥130/85 mmHg, 0.8% (95% CI 0%–1.7%) discontinued for hypertension while among the 192 participants with baseline BP ≥130/85 mmHg and one or more additional cardiovascular risk factors, 1.6% (95% CI 0%–3.3%) discontinued for hypertension.</div></div><div><h3>Conclusions</h3><div>Among >1400 study participants with cardiovascular risk factors using estetrol/drospirenone, only three (0.2%) discontinued for hypertension, all of whom had high-normal baseline BP and at least one other risk cardiovascular risk factor.</div></div><div><h3><strong>Implications</strong></h3><div>Estetrol/drospirenone use demonstrates excellent cardiovascular tolerance in study participants with normal and high-normal blood pressure, even in those with cardiovascular risk factors. The very low rate of hypertension, even when cardiovascular risk factors were present, provides evidence to warrant clinical trials of estetrol/drospirenone in patients with hypertension desiring contraception.</div></div>","PeriodicalId":10762,"journal":{"name":"Contraception","volume":"146 ","pages":"Article 110861"},"PeriodicalIF":2.8000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Estetrol/Drospirenone safety in a population with cardiovascular risk factors\",\"authors\":\"Mitchell D. Creinin , Jean Michel Foidart , Kristina Gemzell-Danielsson , Nina C. 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We found no difference in discontinuation for any adverse events in participants with and without cardiovascular risk factors. Six (0.18%) participants discontinued for a cardiovascular complaint including four with risk factors: three (0.09%) due to hypertension (all had baseline BP ≥130/85 mmHg and one or more additional risk factors) and one due to venous thrombosis (BP ≥130/85 mmHg). Of 375 participants with baseline BP ≥130/85 mmHg, 0.8% (95% CI 0%–1.7%) discontinued for hypertension while among the 192 participants with baseline BP ≥130/85 mmHg and one or more additional cardiovascular risk factors, 1.6% (95% CI 0%–3.3%) discontinued for hypertension.</div></div><div><h3>Conclusions</h3><div>Among >1400 study participants with cardiovascular risk factors using estetrol/drospirenone, only three (0.2%) discontinued for hypertension, all of whom had high-normal baseline BP and at least one other risk cardiovascular risk factor.</div></div><div><h3><strong>Implications</strong></h3><div>Estetrol/drospirenone use demonstrates excellent cardiovascular tolerance in study participants with normal and high-normal blood pressure, even in those with cardiovascular risk factors. 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引用次数: 0
摘要
目的:评价具有心血管危险因素的esteol 15mg/ drosprenone 3mg服用者的心血管安全结局。研究设计:我们对两项开放标签避孕3期试验进行了二次分析,这些试验招募了16至50岁的参与者,使用esteol / drosprerenone长达13个周期。研究排除标准包括:>35岁,吸烟,体重指数>35 kg/m2,基线血压>140/90 mmHg。我们比较了有和没有心血管危险因素的参与者的不良事件发生率,并评估了心血管不良事件的停药率。结果:在3417名参与者中,1410名(41.3%)有一种或多种心血管危险因素,309名(9.0%)有两种或两种以上心血管危险因素。我们发现在有心血管危险因素和没有心血管危险因素的受试者中,任何不良事件的停药没有差异。6名(0.18%)参与者因心血管疾病停药,其中4名有危险因素:3名(0.09%)由于高血压(所有人的基线血压≥130/85 mmHg和一个或多个额外的危险因素),1名由于静脉血栓形成(血压≥130/85 mmHg)。在375名基线血压≥130/85 mmHg的参与者中,0.8% (95% CI 0-1.7%)因高血压停药,而在192名基线血压≥130/85 mmHg并有一个或多个心血管危险因素的参与者中,1.6% (95% CI 0-3.3%)因高血压停药。结论:在bb101400名有心血管危险因素的研究参与者中,只有3人(0.2%)因高血压停药,所有患者基线血压均高于正常水平,且至少有一项其他心血管危险因素。
Estetrol/Drospirenone safety in a population with cardiovascular risk factors
Objectives
To evaluate cardiovascular safety outcomes in estetrol 15 mg/drospirenone 3 mg users with cardiovascular risk factors.
Study design
We performed a secondary analysis of two open-label contraceptive phase-3 trials that enrolled participants 16 to 50 years to use estetrol/drospirenone for up to 13 cycles. Study exclusion criteria included >35 years and smoking, body mass index >35 kg/m2, and baseline blood pressure (BP) >140/90 mmHg. We compared adverse event rates in participants with and without cardiovascular risk factors and assessed discontinuation rates for cardiovascular adverse events.
Results
Of 3417 participants, 1410 (41.3%) had one or more, and 309 (9.0%) had two or more cardiovascular risk factors. We found no difference in discontinuation for any adverse events in participants with and without cardiovascular risk factors. Six (0.18%) participants discontinued for a cardiovascular complaint including four with risk factors: three (0.09%) due to hypertension (all had baseline BP ≥130/85 mmHg and one or more additional risk factors) and one due to venous thrombosis (BP ≥130/85 mmHg). Of 375 participants with baseline BP ≥130/85 mmHg, 0.8% (95% CI 0%–1.7%) discontinued for hypertension while among the 192 participants with baseline BP ≥130/85 mmHg and one or more additional cardiovascular risk factors, 1.6% (95% CI 0%–3.3%) discontinued for hypertension.
Conclusions
Among >1400 study participants with cardiovascular risk factors using estetrol/drospirenone, only three (0.2%) discontinued for hypertension, all of whom had high-normal baseline BP and at least one other risk cardiovascular risk factor.
Implications
Estetrol/drospirenone use demonstrates excellent cardiovascular tolerance in study participants with normal and high-normal blood pressure, even in those with cardiovascular risk factors. The very low rate of hypertension, even when cardiovascular risk factors were present, provides evidence to warrant clinical trials of estetrol/drospirenone in patients with hypertension desiring contraception.
期刊介绍:
Contraception has an open access mirror journal Contraception: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
The journal Contraception wishes to advance reproductive health through the rapid publication of the best and most interesting new scholarship regarding contraception and related fields such as abortion. The journal welcomes manuscripts from investigators working in the laboratory, clinical and social sciences, as well as public health and health professions education.