Treatment of thrombotic cardiovascular diseases in people with haemophilia: A Japanese consensus study

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2024-05-23 DOI:10.1111/hae.15039
Azusa Nagao, Yushi Chikasawa, Yukio Hiroi, Masahiro Ieko
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Abstract

Introduction

Cardiovascular diseases (CVD) that require long-term anticoagulant and antiplatelet therapy presents a problem in people with haemophilia (PWH) who receive factor replacement therapy to reduce bleeding risk. Currently, there are no Japanese guidelines for the management of PWH with CVD.

Aim

To develop expert guidance on managing CVD in PWH in Japan.

Methods

A steering committee of four experts (two haemophilia specialists, one thrombosis specialist, one cardiologist) identified 44 statements related to five key themes. An online questionnaire was produced comprising a mix of 4-point Likert scale and multiple-choice questions that was sent to specialists in the management of PWH with CVD in Japan. Consensus was defined as high or very high if a respective ≥75% or ≥90% of respondents agreed with a statement.

Results

Of 16 potential respondents, responses were received from 15 specialists. Of the Likert scale questions, 71% (29/41) achieved ≥90% agreement (very strong agreement), 17% (7/41) achieved 75%–89% agreement (strong agreement) and 15% (6/41) did not achieve consensus agreement. The three multiple-choice questions failed to identify a strong preference. Agreement on specific target trough clotting factor levels for managing certain clinical situations, such as when in the presence of non-valvular atrial fibrillation or myocardial infarction, was also achieved.

Conclusion

The results of this consensus study provide a framework for cardiologists and haematologists to manage PWH who are at risk of, or who have, CVD. Implementation of the recommendations provided herein may improve outcomes for PWH with CVD.

Abstract Image

血友病患者血栓性心血管疾病的治疗:日本共识研究。
导言:对于接受因子替代治疗以降低出血风险的血友病患者(PWH)来说,需要长期抗凝和抗血小板治疗的心血管疾病(CVD)是一个问题。目前,日本还没有针对患有心血管疾病的血友病患者的管理指南。目的:制定日本血友病患者心血管疾病管理的专家指南:由四位专家(两位血友病专家、一位血栓专家和一位心脏病专家)组成的指导委员会确定了与五个关键主题相关的 44 项声明。我们制作了一份在线问卷,其中包括 4 点李克特量表和多项选择题,并发送给日本心血管疾病患者管理方面的专家。如果有≥75%或≥90%的受访者同意某项陈述,则定义为 "高度共识 "或 "非常高度共识":在 16 位潜在受访者中,收到了 15 位专家的回复。在李克特量表问题中,71%(29/41)的同意率≥90%(非常同意),17%(7/41)的同意率为 75%-89%(非常同意),15%(6/41)未达成一致同意。三道多选题未能确定强烈偏好。在处理某些临床情况(如出现非瓣膜性心房颤动或心肌梗死时)时的特定目标谷值凝血因子水平也达成了一致:这项共识研究的结果为心脏病学家和血液学家提供了一个管理有心血管疾病风险或患有心血管疾病的重症肝炎患者的框架。实施本文提供的建议可改善患有心血管疾病的 PWH 的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Haemophilia
Haemophilia 医学-血液学
CiteScore
6.50
自引率
28.20%
发文量
226
审稿时长
3-6 weeks
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.
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