Acute Compartment Syndrome in Congenital and Acquired Haemophilia.

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

Abstract

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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