Joint and Myofascial Manual Therapy Techniques in Haemophilic Ankle Arthropathy: A Randomized Pilot Study

医学 脚踝 物理疗法 关节病 血友病 随机对照试验 物理医学与康复 外科 骨关节炎 替代医学 病理
作者
Carlos Truque‐Díaz,Javier Meroño‐Gallut,Rubén Cuesta‐Barriuso,Raúl Pérez‐Llanes
出处
期刊:Haemophilia [Wiley]
卷期号:31 (2): 295-303 被引量:1
标识
DOI:10.1111/hae.70002
摘要

ABSTRACT Background Haemophilic ankle arthropathy is characterized by chronic pain, loss of strength and proprioception, decreased range of motion (ROM) and impaired functionality. Objective To evaluate the safety and efficacy of a manual therapy protocol based on joint and myofascial techniques in patients with haemophilic ankle arthropathy. Methods A randomized, single‐blind pilot study. Twenty‐four patients with haemophilia were randomized to the experimental (manual therapy) and control (no intervention) groups. The intervention lasted for 3 weeks, with one 50‐min weekly session. Techniques used: active‐passive joint mobilization, articulatory technique, joint decompression and high‐speed and short‐stroke manipulation, and sustained myofascial induction techniques. The study variables were safety of the intervention (number of hemarthroses), joint pain intensity (visual analogue scale), pressure pain threshold (pressure algometer), range of ankle motion (Leg Motion) and joint condition (Haemophilia Joint Health Score). Results None of the patients developed ankle hemarthrosis during the intervention. After the intervention there were intergroup differences in the variables pain intensity (MD = −0.45; p < 0.001), ROM (MD = 0.19; p = 0.003), joint condition (MD = 0.04; p = 0.03) and pressure pain threshold in the internal malleolus (MD = 1.36; p = 0.01). For the interaction time*group after the follow‐up period, there were statistically significant differences in pain intensity ( F = 6.94; p = 0.01) and dorsal flexion ( F = 3.36; p = 0.04) of the ankle. Conclusions Manual therapy based on joint and myofascial techniques is safe in haemophilia patients. A protocol implementing joint and myofascial techniques having the dosage and safety parameters established in this study can improve the intensity of pain and dorsal flexion of the ankle in these patients. Trial Registration ClinicalTrials.gov identifier: NCT05549843
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