4.6 Article

Oral estradiol/micronized progesterone may be associated with lower risk of venous thromboembolism compared with conjugated equine estrogens/ medroxyprogesterone acetate in real-world practice

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MATURITAS
卷 172, 期 -, 页码 23-31

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ELSEVIER IRELAND LTD
DOI: 10.1016/j.maturitas.2023.04.004

关键词

Venous thromboembolism; 17 beta-Estradiol/micronized progesterone; Conjugated equine estrogens/medroxyprogesterone acetate; Menopause; Hormone therapy; Safety

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This study compared the risk of venous thromboembolism between women treated with oral 17 beta-estradiol/micronized progesterone (E2/P4) and those treated with oral conjugated equine estrogens/medroxyprogesterone acetate (CEE/MPA). The study found that women receiving oral E2/P4 had a significantly lower risk of venous thromboembolism compared with those receiving oral CEE/MPA.
Objectives: The Women's Health Initiative study reported an increased risk of venous thromboembolism among menopausal women treated with conjugated equine estrogens/medroxyprogesterone acetate (CEE/MPA) versus placebo. Newer hormone therapies may have a lower venous thromboembolism risk. The study compared the risk of venous thromboembolism between women treated with the combined oral product 17 beta-estradiol/ micronized progesterone (E2/P4) and those treated with oral CEE/MPA regimens. Study design: In a retrospective longitudinal study using real-world claims data from April 2019 to June 2021, women aged 40 years or more treated with oral E2/P4 or oral CEE/MPA who did not have a venous thromboembolism diagnosis before first dispensing claim of CEE/MPA or E2/P4 identified on or after May 1st 2019 (index date) were observed for 6 months or more after the index date. Oral E2/P4 and oral CEE/MPA had been prescribed by the treating physician in real-world practice and were observed through pharmacy dispensing records. Main outcome measures: Venous thromboembolism risk was compared between women receiving oral E2/P4 versus oral CEE/MPA. Results: The study included 36,061 women treated with oral E2/P4 or oral CEE/MPA. In the analyses weighted by the inverse probability of treatment for control of potential confounding factors, the incidence of venous thromboembolism was significantly lower for oral E2/P4 compared with oral CEE/MPA (37/10,000 womenyears for oral E2/P4 vs 53/10,000 women-years for oral CEE/MPA; incidence rate ratio 0.70, 95 % confidence interval: 0.53-0.92). Conclusions: Real-world evidence suggests that the risk of venous thromboembolism is significantly lower among women treated with oral E2/P4 compared with oral CEE/MPA.

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