Catherine A Sims, Brian Perry, Christine Yeung, Heather Tam, Joyce Kullman, Renée L Borchin, Cristina Burroughs, Peter A Merkel, Megan E B Clowse
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Participant responses were evaluated using thematic analysis.</p><p><strong>Results: </strong>Eighteen patients with vasculitis who had experienced pregnancy were interviewed (10 antineutrophil cytoplasmic antibody-associated vasculitis, 4 Takayasu arteritis, 2 Behçet disease, 1 IgA vasculitis, 1 relapsing polychondritis). Thematic analysis revealed common experiences in the decision-making process during pregnancy planning, including accessing information from multiple sources, communicating with medical professionals, and changing treatment for vasculitis. Women sought information about vasculitis and pregnancy from various sources, including social media; however, opinions from their physicians and family members were most influential. Patients were more likely than providers to initiate conversations regarding family planning. Balancing differing opinions from subspecialists was challenging as many patients recalled acting as a liaison between multiple physicians during pregnancy. The need for self-advocacy was a common experience among patients. Most women had pregnancies that resulted in live births with delivery at term.</p><p><strong>Conclusion: </strong>When making decisions about pregnancy, women of reproductive age with vasculitis used multiple resources. Patients consistently valued their medical provider's opinion over alternative sources of information. To ensure comprehensive medical care, half of women relied on self-advocacy to coordinate communication among subspecialists. Most women had pregnancies that resulted in live births with delivery at term.</p>","PeriodicalId":50064,"journal":{"name":"Journal of Rheumatology","volume":null,"pages":null},"PeriodicalIF":3.6000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exploring Reproductive Experiences With Women Enrolled in the International Vasculitis Pregnancy Registry.\",\"authors\":\"Catherine A Sims, Brian Perry, Christine Yeung, Heather Tam, Joyce Kullman, Renée L Borchin, Cristina Burroughs, Peter A Merkel, Megan E B Clowse\",\"doi\":\"10.3899/jrheum.2023-1055\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>This study explored the reproductive journeys of women with vasculitis, including their conversations with healthcare providers, disease activity, medication changes, and delivery experiences.</p><p><strong>Methods: </strong>Interviews were conducted with women registered in the Vasculitis Pregnancy Registry (VPREG), an online patient-reported registry of pregnant women with vasculitis. A team of physicians, patients, and qualitative researchers developed a qualitative interview guide. Participant responses were evaluated using thematic analysis.</p><p><strong>Results: </strong>Eighteen patients with vasculitis who had experienced pregnancy were interviewed (10 antineutrophil cytoplasmic antibody-associated vasculitis, 4 Takayasu arteritis, 2 Behçet disease, 1 IgA vasculitis, 1 relapsing polychondritis). Thematic analysis revealed common experiences in the decision-making process during pregnancy planning, including accessing information from multiple sources, communicating with medical professionals, and changing treatment for vasculitis. Women sought information about vasculitis and pregnancy from various sources, including social media; however, opinions from their physicians and family members were most influential. Patients were more likely than providers to initiate conversations regarding family planning. Balancing differing opinions from subspecialists was challenging as many patients recalled acting as a liaison between multiple physicians during pregnancy. The need for self-advocacy was a common experience among patients. Most women had pregnancies that resulted in live births with delivery at term.</p><p><strong>Conclusion: </strong>When making decisions about pregnancy, women of reproductive age with vasculitis used multiple resources. Patients consistently valued their medical provider's opinion over alternative sources of information. To ensure comprehensive medical care, half of women relied on self-advocacy to coordinate communication among subspecialists. 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引用次数: 0
摘要
目的:本研究探讨了患有脉管炎的女性的生育历程,包括她们与医疗服务提供者的对话、疾病活动、药物变化和分娩经历:本研究探讨了患有脉管炎的女性的生育历程,包括她们与医疗服务提供者的对话、疾病活动、药物变化和分娩经历:对在脉管炎妊娠登记处(VPREG)登记的女性进行了访谈,该登记处是脉管炎妊娠女性的在线患者报告登记处。由医生、患者和定性研究人员组成的团队制定了一份定性访谈指南。结果:对 18 名有过妊娠经历的血管炎患者(10 名抗中性粒细胞胞浆抗体相关性血管炎患者、4 名高安动脉炎患者、2 名白塞氏病患者、1 名 IgA 血管炎患者、1 名复发性多软骨炎患者)进行了访谈。专题分析揭示了在计划怀孕期间决策过程中的共同经历,包括从多种渠道获取信息、与医疗专业人员沟通以及改变脉管炎的治疗方法。女性从各种渠道(包括社交媒体)寻求有关脉管炎和怀孕的信息;然而,医生和家庭成员的意见对她们的影响最大。患者比医护人员更有可能主动提出有关计划生育的谈话。平衡来自亚专科医生的不同意见具有挑战性,因为许多患者回忆说,他们在怀孕期间充当了多位医生之间的联络人。需要自我主张是患者的共同经历。大多数妇女的妊娠结果都是活产和足月分娩:结论:患有血管炎的育龄妇女在做出怀孕决定时会利用多种资源。与其他信息来源相比,患者更看重医疗服务提供者的意见。为了确保获得全面的医疗护理,半数妇女依靠自我宣传来协调亚专科医生之间的沟通。大多数妇女的妊娠结果都是活产和足月分娩。
Exploring Reproductive Experiences With Women Enrolled in the International Vasculitis Pregnancy Registry.
Objective: This study explored the reproductive journeys of women with vasculitis, including their conversations with healthcare providers, disease activity, medication changes, and delivery experiences.
Methods: Interviews were conducted with women registered in the Vasculitis Pregnancy Registry (VPREG), an online patient-reported registry of pregnant women with vasculitis. A team of physicians, patients, and qualitative researchers developed a qualitative interview guide. Participant responses were evaluated using thematic analysis.
Results: Eighteen patients with vasculitis who had experienced pregnancy were interviewed (10 antineutrophil cytoplasmic antibody-associated vasculitis, 4 Takayasu arteritis, 2 Behçet disease, 1 IgA vasculitis, 1 relapsing polychondritis). Thematic analysis revealed common experiences in the decision-making process during pregnancy planning, including accessing information from multiple sources, communicating with medical professionals, and changing treatment for vasculitis. Women sought information about vasculitis and pregnancy from various sources, including social media; however, opinions from their physicians and family members were most influential. Patients were more likely than providers to initiate conversations regarding family planning. Balancing differing opinions from subspecialists was challenging as many patients recalled acting as a liaison between multiple physicians during pregnancy. The need for self-advocacy was a common experience among patients. Most women had pregnancies that resulted in live births with delivery at term.
Conclusion: When making decisions about pregnancy, women of reproductive age with vasculitis used multiple resources. Patients consistently valued their medical provider's opinion over alternative sources of information. To ensure comprehensive medical care, half of women relied on self-advocacy to coordinate communication among subspecialists. Most women had pregnancies that resulted in live births with delivery at term.
期刊介绍:
The Journal of Rheumatology is a monthly international serial edited by Earl D. Silverman. The Journal features research articles on clinical subjects from scientists working in rheumatology and related fields, as well as proceedings of meetings as supplements to regular issues. Highlights of our 41 years serving Rheumatology include: groundbreaking and provocative editorials such as "Inverting the Pyramid," renowned Pediatric Rheumatology, proceedings of OMERACT and the Canadian Rheumatology Association, Cochrane Musculoskeletal Reviews, and supplements on emerging therapies.