Department of Orthopaedic Surgery and Sports Medicine, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Department of Orthopaedic Surgery and Sports Medicine, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
J Sci Med Sport. 2021 Sep;24(9):871-875. doi: 10.1016/j.jsams.2021.04.001. Epub 2021 Apr 19.
To analyse whether (1) passive or active pain coping strategies and (2) presence of neuropathic pain component influences the change of Achilles tendinopathy (AT) symptoms over a course of 24 weeks in conservatively-treated patients.
Prospective cohort study.
Patients with clinically-diagnosed chronic midportion AT were conservatively treated. At baseline, the Pain Coping Inventory (PCI) was used to determine scores of coping, which consisted of two domains, active and passive (score ranging from 0 to 1; the higher, the more active or passive). Presence of neuropathic pain (PainDETECT questionnaire, -1 to 38 points) was categorized as (a) unlikely (≤12 points), (b) unclear (13-18 points) and (c) likely (≥19 points). The symptom severity was determined with the validated Victorian Institute of Sports Assessment-Achilles (VISA-A) questionnaire (0-100) at baseline, 6, 12 and 24 weeks. We analysed the correlation between (1) PCI and (2) PainDETECT baseline scores with change in VISA-A score using an adjusted Generalized Estimating Equations model.
Of 80 included patients, 76 (95%) completed the 24-weeks follow-up. The mean VISA-A score (standard deviation) increased from 43 (16) points at baseline to 63 (23) points at 24 weeks. Patients had a mean (standard deviation) active coping score of 0.53 (0.13) and a passive score of 0.43 (0.10). Twelve patients (15%) had a likely neuropathic pain component. Active and passive coping mechanisms and presence of neuropathic pain did not influence the change in AT symptoms (p=0.459, p=0.478 and p=0.420, respectively).
Contrary to widespread belief, coping strategy and presence of neuropathic pain are not associated with a worse clinical outcome in this homogeneous group of patients with clinically diagnosed AT.
分析被动或主动疼痛应对策略(1)以及是否存在神经病理性疼痛成分(2)是否会影响保守治疗患者 24 周内跟腱病(AT)症状的变化。
前瞻性队列研究。
对临床诊断为慢性中段 AT 的患者进行保守治疗。在基线时,使用疼痛应对量表(PCI)确定应对策略的评分,该量表由两个域组成,主动和被动(评分范围为 0 到 1;得分越高,主动或被动程度越高)。神经病理性疼痛的存在(疼痛 DETECT 问卷,-1 到 38 分)分为(a)不太可能(≤12 分)、(b)不确定(13-18 分)和(c)很可能(≥19 分)。在基线、6、12 和 24 周时,使用经过验证的维多利亚运动评估-跟腱(VISA-A)问卷(0-100)确定症状严重程度。我们使用调整后的广义估计方程模型分析了(1)PCI 和(2)基线时 PainDETECT 评分与 VISA-A 评分变化之间的相关性。
在 80 名纳入的患者中,76 名(95%)完成了 24 周的随访。VISA-A 评分(标准差)从基线时的 43(16)分增加到 24 周时的 63(23)分。患者的平均(标准差)主动应对得分为 0.53(0.13),被动应对得分为 0.43(0.10)。12 名患者(15%)存在很可能的神经病理性疼痛成分。主动和被动应对机制以及神经病理性疼痛的存在均未影响 AT 症状的变化(p=0.459,p=0.478 和 p=0.420)。
与普遍看法相反,在这组同质的临床诊断为 AT 的患者中,应对策略和神经病理性疼痛的存在与较差的临床结局无关。