先天性和获得性血友病的急性间室综合征。

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2025-03-23 DOI:10.1111/hae.70036
Emerito Carlos Rodriguez-Merchan, Binoy Yohannan, Miguel A Escobar
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引用次数: 0

摘要

背景:急性筋膜间室综合征(ACS)是一种外科急诊,定义为筋膜间室肌内压力升高,危及毛细血管灌注并威胁筋膜间室组织的生存。筋膜室压力的持续增加导致神经和肌肉不可逆的坏死,导致永久性损伤。目的:对先天性和获得性血友病(PwH)患者ACS诊断和治疗的文献进行综述。方法:以“血友病和室室综合征”为关键词,在PubMed (MEDLINE)和Cochrane图书馆检索2024年2月28日之前发表的文章。结果:我们在PubMed中发现77篇(其中19篇因与主题不严格相关而被淘汰),在Cochrane Library中发现1篇(在PubMed中重复)。总共有83例已发表的病例(61例先天性血友病,22例获得性血友病)。结论:对患有ACS的PwH患者进行误诊或早期血液学治疗失败,如果血液学治疗不能阻止问题,则进行广泛的筋膜切开术,可能导致患肢永久性残疾。预后取决于室压升高的强度和持续时间。对于PwH,适当的凝血因子替代应该是治疗的第一步,因为它可能对某些ACS病例有效。围手术期一般应维持50% ~ 100%的因子水平;此后,剂量可逐渐减少至维持50%的水平约2周,必要时可更长时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute Compartment Syndrome in Congenital and Acquired Haemophilia.

Background: Acute compartment syndrome (ACS) is a surgical emergency defined as an increase in intramuscular pressure within a compartment that compromises capillary perfusion and threatens the survival of compartment tissues. A sustained increase in compartment pressure causes irreversible necrosis of nerves and muscles, leading to permanent damage.

Purpose: To conduct a narrative review of the literature on the diagnosis and treatment of ACS in persons with congenital and acquired haemophilia (PwH) METHODS: An English-language literature search for articles published before 28 February 2024 was performed in PubMed (MEDLINE) and the Cochrane Library using "haemophilia and compartment syndrome" as keywords.

Results: We found 77 articles in PubMed (of which 19 were eliminated as not strictly related to the topic) and 1 in the Cochrane Library (which was repeated in PubMed). In total, there are 83 published cases (61 of congenital haemophilia and 22 of acquired haemophilia).

Conclusions: Misdiagnosis or failure to perform early haematological treatment in PwH suffering from ACS, followed by extensive fasciotomy if haematological treatment does not stop the problem, may result in permanent disability of the affected limb. The prognosis will depend on the intensity and duration of the compartment pressure elevation. For PwH, adequate clotting factor replacement should be the first step of treatment, as it may be effective in some cases of ACS. In general, factor levels of 50%-100% should be maintained in the perioperative period; thereafter, the dose can be gradually reduced to maintain levels at 50% for approximately 2 weeks or longer if necessary.

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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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