Mayank Patel, Victor Zibara, Craig Seaman, Sruti Shiva, Nicoletta C Machin
{"title":"Risk of Postpartum Hemorrhage in Women With Von Willebrand Disease: A Real-World Data Analysis.","authors":"Mayank Patel, Victor Zibara, Craig Seaman, Sruti Shiva, Nicoletta C Machin","doi":"10.1111/hae.70400","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Women with von Willebrand disease (VWD) are at increased risk for postpartum hemorrhage (PPH), but contemporary United States data on maternal outcomes and real-world peripartum treatment patterns are limited.</p><p><strong>Aim: </strong>To evaluate maternal outcomes associated with claims-recorded VWD in a national claims cohort and describe exploratory treatment and geozip analyses.</p><p><strong>Methods: </strong>We retrospectively analyzed FAIR Health claims from 2011-2021. Delivery encounters, VWD, and outcomes were identified using ICD-9/10 codes; laboratory confirmation was unavailable. Logistic regression estimated odds ratios (ORs) and 95% confidence intervals (CIs) for PPH, length of stay above the median, 30-day emergency department visit or readmission, and in-hospital mortality.</p><p><strong>Results: </strong>Among 1,498,768 delivery encounters, 1,514 (0.10%) involved claims-recorded VWD. Overall outcome frequencies were 3.79% for PPH, 24.81% for length of stay above the median, 7.43% for 30-day utilization, and 0.036% for mortality. Claims-recorded VWD was associated with PPH (OR 1.70, 95% CI 1.38-2.10), length of stay above the median (OR 1.58, 95% CI 1.41-1.78), and 30-day utilization (OR 1.20, 95% CI 1.01-1.43), but not mortality (OR 1.79, 95% CI 0.25-12.73). In exploratory analyses, VWF concentrate claims were associated with higher PPH odds versus neither captured desmopressin nor VWF concentrate (OR 3.17, 95% CI 1.28-7.87); desmopressin showed a similar non-significant pattern (OR 3.32, 95% CI 0.93-11.82).</p><p><strong>Conclusion: </strong>Claims-recorded VWD was associated with PPH and greater peripartum healthcare utilization. Exploratory treatment associations may reflect confounding by indication, diagnostic misclassification, or treatment timing and cannot establish benefit or harm. Prospective studies incorporating laboratory and clinical data are needed.</p><p><strong>Plain language summary: </strong>Von Willebrand disease is the most common inherited bleeding disorder. For many women, it can cause heavy periods and can also increase the risk of heavy bleeding after delivery, called postpartum haemorrhage. Even though this risk is well recognised, there is still limited information about what happens in real-world delivery care across the United States. In this study, we looked at a large national insurance claims database that included almost 1.5 million delivery encounters from 2011 to 2021. Of these, 1,514 were among women with von Willebrand disease. Compared with women without von Willebrand disease, women with von Willebrand disease had higher odds of postpartum haemorrhage, longer hospital stays, and emergency department visits or readmissions within 30 days of delivery. We also looked at outcomes among women with von Willebrand disease based on whether treatment was documented in the claims data. Women who had claims for von Willebrand factor concentrate or desmopressin had higher observed odds of postpartum haemorrhage than women without documented treatment. This does not mean that the treatment caused bleeding. More likely, these women were treated because they were already considered to be at higher risk, had more severe disease, were actively bleeding, or raised greater concern for their clinical team. Overall, this study shows that postpartum bleeding remains an important and ongoing issue for women with von Willebrand disease. Future studies should include laboratory results, bleeding history, details about treatment timing and dose, delivery setting, and access to specialised bleeding disorder care. These details are needed to better understand which patients are at highest risk and how to improve the prevention of postpartum haemorrhage.</p>","PeriodicalId":12819,"journal":{"name":"Haemophilia","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2026-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Haemophilia","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/hae.70400","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Women with von Willebrand disease (VWD) are at increased risk for postpartum hemorrhage (PPH), but contemporary United States data on maternal outcomes and real-world peripartum treatment patterns are limited.
Aim: To evaluate maternal outcomes associated with claims-recorded VWD in a national claims cohort and describe exploratory treatment and geozip analyses.
Methods: We retrospectively analyzed FAIR Health claims from 2011-2021. Delivery encounters, VWD, and outcomes were identified using ICD-9/10 codes; laboratory confirmation was unavailable. Logistic regression estimated odds ratios (ORs) and 95% confidence intervals (CIs) for PPH, length of stay above the median, 30-day emergency department visit or readmission, and in-hospital mortality.
Results: Among 1,498,768 delivery encounters, 1,514 (0.10%) involved claims-recorded VWD. Overall outcome frequencies were 3.79% for PPH, 24.81% for length of stay above the median, 7.43% for 30-day utilization, and 0.036% for mortality. Claims-recorded VWD was associated with PPH (OR 1.70, 95% CI 1.38-2.10), length of stay above the median (OR 1.58, 95% CI 1.41-1.78), and 30-day utilization (OR 1.20, 95% CI 1.01-1.43), but not mortality (OR 1.79, 95% CI 0.25-12.73). In exploratory analyses, VWF concentrate claims were associated with higher PPH odds versus neither captured desmopressin nor VWF concentrate (OR 3.17, 95% CI 1.28-7.87); desmopressin showed a similar non-significant pattern (OR 3.32, 95% CI 0.93-11.82).
Conclusion: Claims-recorded VWD was associated with PPH and greater peripartum healthcare utilization. Exploratory treatment associations may reflect confounding by indication, diagnostic misclassification, or treatment timing and cannot establish benefit or harm. Prospective studies incorporating laboratory and clinical data are needed.
Plain language summary: Von Willebrand disease is the most common inherited bleeding disorder. For many women, it can cause heavy periods and can also increase the risk of heavy bleeding after delivery, called postpartum haemorrhage. Even though this risk is well recognised, there is still limited information about what happens in real-world delivery care across the United States. In this study, we looked at a large national insurance claims database that included almost 1.5 million delivery encounters from 2011 to 2021. Of these, 1,514 were among women with von Willebrand disease. Compared with women without von Willebrand disease, women with von Willebrand disease had higher odds of postpartum haemorrhage, longer hospital stays, and emergency department visits or readmissions within 30 days of delivery. We also looked at outcomes among women with von Willebrand disease based on whether treatment was documented in the claims data. Women who had claims for von Willebrand factor concentrate or desmopressin had higher observed odds of postpartum haemorrhage than women without documented treatment. This does not mean that the treatment caused bleeding. More likely, these women were treated because they were already considered to be at higher risk, had more severe disease, were actively bleeding, or raised greater concern for their clinical team. Overall, this study shows that postpartum bleeding remains an important and ongoing issue for women with von Willebrand disease. Future studies should include laboratory results, bleeding history, details about treatment timing and dose, delivery setting, and access to specialised bleeding disorder care. These details are needed to better understand which patients are at highest risk and how to improve the prevention of postpartum haemorrhage.
患有血管性血友病(VWD)的妇女产后出血(PPH)的风险增加,但当代美国关于产妇结局和现实世界围产期治疗模式的数据有限。目的:在国家索赔队列中评估与索赔记录的VWD相关的产妇结局,并描述探索性治疗和地理zip分析。方法:回顾性分析2011-2021年FAIR健康声明。使用ICD-9/10代码确定分娩遭遇、VWD和结果;无法获得实验室确认。Logistic回归估计PPH的优势比(ORs)和95%置信区间(ci)、住院时间超过中位数、30天急诊或再入院以及院内死亡率。结果:在1,498,768例分娩中,1,514例(0.10%)涉及索赔记录的VWD。PPH的总结局频率为3.79%,中位数以上住院时间为24.81%,30天利用率为7.43%,死亡率为0.036%。索赔记录的VWD与PPH (OR 1.70, 95% CI 1.38-2.10)、中位数以上住院时间(OR 1.58, 95% CI 1.41-1.78)和30天利用率(OR 1.20, 95% CI 1.01-1.43)相关,但与死亡率无关(OR 1.79, 95% CI 0.25-12.73)。在探索性分析中,与捕获去氨加压素和VWF浓缩物相比,VWF浓缩物声称与更高的PPH几率相关(OR 3.17, 95% CI 1.28-7.87);去氨加压素表现出类似的无显著性模式(OR 3.32, 95% CI 0.93-11.82)。结论:理赔记录的VWD与PPH和更多围产期保健利用有关。探索性治疗关联可能反映了适应症、诊断错误分类或治疗时机的混淆,不能确定是有益还是有害。需要结合实验室和临床数据的前瞻性研究。摘要:血管性血友病是最常见的遗传性出血性疾病。对许多女性来说,它会导致月经量大,也会增加分娩后大出血的风险,也就是产后大出血。尽管这种风险是公认的,但关于美国真实分娩护理中发生的情况的信息仍然有限。在这项研究中,我们研究了一个大型的国家保险索赔数据库,其中包括2011年至2021年期间近150万次送货遭遇。其中,1514人是患有血管性血友病的妇女。与没有血管性血友病的妇女相比,患有血管性血友病的妇女产后出血的几率更高,住院时间更长,分娩后30天内急诊或再入院的几率更高。我们还观察了患有血管性血友病的妇女的结果,根据治疗是否记录在索赔数据中。声称服用浓缩血管性血友病因子或去氨加压素的妇女比未接受治疗的妇女观察到的产后出血的几率更高。这并不意味着治疗会导致出血。更有可能的是,这些女性接受治疗是因为她们已经被认为处于更高的风险中,患有更严重的疾病,正在活跃地出血,或者引起了临床团队的更大关注。总的来说,这项研究表明,产后出血仍然是血管性血友病妇女的一个重要和持续的问题。未来的研究应包括实验室结果、出血史、治疗时间和剂量的细节、分娩环境以及获得专门的出血性疾病护理的机会。需要这些细节来更好地了解哪些患者的风险最高,以及如何改善产后出血的预防。
期刊介绍:
Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include:
clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI
replacement therapy for clotting factor deficiencies
component therapy in the developing world
transfusion transmitted disease
haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics
nursing
laboratory diagnosis
carrier detection
psycho-social concerns
economic issues
audit
inherited platelet disorders.