Do women with venous thromboembolism bleed more than men during anticoagulation? Data from the real-life, prospective START-Register.

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Drug Safety Pub Date : 2021-12-16 eCollection Date: 2021-01-01 DOI:10.1177/20420986211062965
Gualtiero Palareti, Cristina Legnani, Emilia Antonucci, Benilde Cosmi, Anna Falanga, Daniela Poli, Daniela Mastroiacovo, Vittorio Pengo, Walter Ageno, Sophie Testa
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Furthermore, analyses of clinical trials reported an abnormal vaginal bleeding in women of reproductive age treated with DOACs. This study aimed at comparing the risk of bleeding in an inception cohort of VTE women and men included in a prospective observational registry.</p><p><strong>Methods: </strong>Baseline characteristics and bleeding events occurring during anticoagulation in patients of both sexes, included in the START-Register after a first VTE, were analyzed.</p><p><strong>Results: </strong>In all, 1298 women were compared with 1290 men. Women were older and more often had renal diseases; their index events were often provoked (often by hormonal contraception and pregnancy), and more frequently presented as isolated pulmonary embolism (PE). The rate of bleeding was similar in women (2.9% patient-years) and men (2.1% patient-years), though it was higher when uterine bleeds were included (3.5% patient-years, <i>p</i> = 0.0141). More bleeds occurred in VKA- than DOAC-treated patients (6.4% <i>versus</i> 2.6%, respectively; <i>p</i> = 0.0013). At multivariate analysis, age ⩾ 75 years was associated with higher prevalence of bleeds.</p><p><strong>Conclusion: </strong>The occurrence of bleeding was not different between women and men during anticoagulation after VTE. Only after inclusion of vaginal/uterine bleeds, the rate of bleeding was higher in women. The incidence of bleeding was higher in women treated with VKAs.</p><p><strong>Plain language summary: </strong><b>The risk of bleeding in women anticoagulated for deep vein thrombosis or pulmonary embolism is not higher than that in men, except for vaginal bleeding:</b> <b>Background::</b> The occurrence of a venous thromboembolic event (VTE, including deep vein thrombosis and pulmonary embolism) necessarily requires a period of at least 3-6 months of treatment with anticoagulant drugs [either vitamin k antagonists (VKA) or, more recently, direct oral anticoagulants (DOACs)]. Anticoagulation therapy, however, is associated with a risk of bleeding that is influenced by several factors. Sex is one of these factors as some authors have hypothesized that women are at higher risk than men. Furthermore, some studies have recently found more vaginal bleeding in VTE women treated with a DOAC compared with those who received VKAs.<b>Methods::</b> The present study aimed to compare the frequency of bleeds occurring in women and in men who were treated with DOACs or VKAs for a first VTE event and followed in real-life conditions. Since the beginning of their anticoagulant treatment, the patients were included in a prospective, multicenter, observational registry (the START-Register), and bleeding events were recorded.<b>Results::</b> A total of 1298 women were compared with 1290 men. Women were older and more often were affected by renal diseases; their VTE events were often associated with risk factors (especially hormonal contraception and pregnancy) and presented as isolated pulmonary embolism. The rate of all bleeding events (including major, non-major but clinically relevant, and minor bleeds) was higher in women (3.5% patient-years) than in men (2.1% patient-years, <i>p</i> = 0.0141); however, the difference was no longer statistically significant after exclusion of uterine bleeds (2.9% patient years). More bleeding occurred in women receiving VKA as anticoagulant drug compared with those treated with a DOAC (6.4% <i>versus</i> 2.6%, respectively; <i>p</i> = 0.0013). At multivariate analysis, age ⩾ 75 years was associated with higher prevalence of bleeds.<b>Conclusion::</b> In conclusion, we found that in real-life conditions, the rate of bleeding events occurring during anticoagulation after a VTE episode is not higher in women than in men. Only after inclusion of vaginal bleeds, the rate of bleeding was higher in women. 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引用次数: 4

Abstract

Background: Venous thromboembolism (VTE) is a frequent and serious disease that requires immediate and long-term anticoagulant treatment, which is inevitably associated with a risk of bleeding complications. Some studies, though not all, reported a higher risk of bleeding in female patients treated with either old anticoagulants [vitamin k antagonists (VKAs)] or recent anticoagulants [direct oral anticoagulants (DOACs)]. Furthermore, analyses of clinical trials reported an abnormal vaginal bleeding in women of reproductive age treated with DOACs. This study aimed at comparing the risk of bleeding in an inception cohort of VTE women and men included in a prospective observational registry.

Methods: Baseline characteristics and bleeding events occurring during anticoagulation in patients of both sexes, included in the START-Register after a first VTE, were analyzed.

Results: In all, 1298 women were compared with 1290 men. Women were older and more often had renal diseases; their index events were often provoked (often by hormonal contraception and pregnancy), and more frequently presented as isolated pulmonary embolism (PE). The rate of bleeding was similar in women (2.9% patient-years) and men (2.1% patient-years), though it was higher when uterine bleeds were included (3.5% patient-years, p = 0.0141). More bleeds occurred in VKA- than DOAC-treated patients (6.4% versus 2.6%, respectively; p = 0.0013). At multivariate analysis, age ⩾ 75 years was associated with higher prevalence of bleeds.

Conclusion: The occurrence of bleeding was not different between women and men during anticoagulation after VTE. Only after inclusion of vaginal/uterine bleeds, the rate of bleeding was higher in women. The incidence of bleeding was higher in women treated with VKAs.

Plain language summary: The risk of bleeding in women anticoagulated for deep vein thrombosis or pulmonary embolism is not higher than that in men, except for vaginal bleeding: Background:: The occurrence of a venous thromboembolic event (VTE, including deep vein thrombosis and pulmonary embolism) necessarily requires a period of at least 3-6 months of treatment with anticoagulant drugs [either vitamin k antagonists (VKA) or, more recently, direct oral anticoagulants (DOACs)]. Anticoagulation therapy, however, is associated with a risk of bleeding that is influenced by several factors. Sex is one of these factors as some authors have hypothesized that women are at higher risk than men. Furthermore, some studies have recently found more vaginal bleeding in VTE women treated with a DOAC compared with those who received VKAs.Methods:: The present study aimed to compare the frequency of bleeds occurring in women and in men who were treated with DOACs or VKAs for a first VTE event and followed in real-life conditions. Since the beginning of their anticoagulant treatment, the patients were included in a prospective, multicenter, observational registry (the START-Register), and bleeding events were recorded.Results:: A total of 1298 women were compared with 1290 men. Women were older and more often were affected by renal diseases; their VTE events were often associated with risk factors (especially hormonal contraception and pregnancy) and presented as isolated pulmonary embolism. The rate of all bleeding events (including major, non-major but clinically relevant, and minor bleeds) was higher in women (3.5% patient-years) than in men (2.1% patient-years, p = 0.0141); however, the difference was no longer statistically significant after exclusion of uterine bleeds (2.9% patient years). More bleeding occurred in women receiving VKA as anticoagulant drug compared with those treated with a DOAC (6.4% versus 2.6%, respectively; p = 0.0013). At multivariate analysis, age ⩾ 75 years was associated with higher prevalence of bleeds.Conclusion:: In conclusion, we found that in real-life conditions, the rate of bleeding events occurring during anticoagulation after a VTE episode is not higher in women than in men. Only after inclusion of vaginal bleeds, the rate of bleeding was higher in women. More bleeds (including vaginal bleeding) occurred in women treated with VKA than DOACs.

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女性静脉血栓栓塞患者在抗凝期间出血比男性多吗?数据来自现实生活中,未来的START-Register。
背景:静脉血栓栓塞(VTE)是一种常见且严重的疾病,需要立即和长期的抗凝治疗,不可避免地与出血并发症的风险相关。一些研究,虽然不是全部,报道了使用旧抗凝剂[维生素k拮抗剂(VKAs)]或新抗凝剂[直接口服抗凝剂(DOACs)]治疗的女性患者出血风险更高。此外,临床试验分析报告了DOACs治疗育龄妇女阴道异常出血。本研究旨在比较前瞻性观察登记的静脉血栓栓塞女性和男性初始队列的出血风险。方法:分析首次静脉血栓栓塞后START-Register患者的基线特征和抗凝期间发生的出血事件。结果:总共有1298名女性和1290名男性。妇女年龄较大,更常患有肾脏疾病;它们的指标事件通常是由激素避孕和怀孕引起的,更常见的是孤立性肺栓塞(PE)。女性(2.9%患者-年)和男性(2.1%患者-年)的出血率相似,但当包括子宫出血时,出血率更高(3.5%患者-年,p = 0.0141)。VKA组出血发生率高于doac组(分别为6.4%和2.6%;P = 0.0013)。在多变量分析中,年龄大于或等于75岁与较高的出血发生率相关。结论:静脉血栓栓塞术后抗凝期间出血的发生率男女无差异。只有在纳入阴道/子宫出血后,女性的出血率才更高。使用vka治疗的女性出血发生率较高。简单的语言总结:除阴道出血外,女性抗凝治疗深静脉血栓形成或肺栓塞的出血风险并不高于男性。背景:静脉血栓栓塞事件(VTE,包括深静脉血栓形成和肺栓塞)的发生必然需要至少3-6个月的抗凝药物治疗[维生素k拮抗剂(VKA)或最近的直接口服抗凝剂(DOACs)]。然而,抗凝治疗与出血风险相关,出血风险受几个因素的影响。性是其中一个因素,一些作者假设女性比男性有更高的风险。此外,最近的一些研究发现,与接受vka治疗的女性相比,接受DOAC治疗的VTE女性阴道出血更多。方法:本研究旨在比较首次静脉血栓栓塞事件接受doac或vka治疗的女性和男性的出血频率,并在现实生活中进行随访。自开始抗凝治疗以来,患者被纳入前瞻性、多中心、观察性登记(START-Register),并记录出血事件。结果:女性1298人,男性1290人。妇女年龄较大,更常受到肾脏疾病的影响;他们的静脉血栓栓塞事件通常与危险因素(尤其是激素避孕和怀孕)有关,并表现为孤立性肺栓塞。所有出血事件(包括重大、非重大但临床相关的出血和轻微出血)的发生率,女性(3.5%患者-年)高于男性(2.1%患者-年,p = 0.0141);然而,在排除子宫出血(2.9%患者年)后,差异不再具有统计学意义。与DOAC相比,接受VKA作为抗凝药物的女性出血发生率更高(分别为6.4%和2.6%;P = 0.0013)。在多变量分析中,年龄大于或等于75岁与较高的出血发生率相关。结论:总之,我们发现在现实生活条件下,静脉血栓栓塞发作后抗凝期间出血事件的发生率在女性中并不高于男性。只有在纳入阴道出血后,女性的出血率才更高。VKA治疗的妇女出血(包括阴道出血)多于DOACs。
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来源期刊
Therapeutic Advances in Drug Safety
Therapeutic Advances in Drug Safety Medicine-Pharmacology (medical)
CiteScore
6.70
自引率
4.50%
发文量
31
审稿时长
9 weeks
期刊介绍: Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in drug safety, providing a forum in print and online for publishing the highest quality articles in this area. The editors welcome articles of current interest on research across all areas of drug safety, including therapeutic drug monitoring, pharmacoepidemiology, adverse drug reactions, drug interactions, pharmacokinetics, pharmacovigilance, medication/prescribing errors, risk management, ethics and regulation.
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