Validation and cultural adaption of the neuropathic pain screening questionnaire painDETECT in Chinese

Howan Leung, Josephine W.Y. Ip, J. Lam, Gavin K.W. Lee, Carina C.F. Li, Richard Li, Vincent Mok, Tak H. Tsoi, Chun P. Wong, Steven H.S. Wong, Chun M. Chang, Rainer Freynhagen
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Abstract

Aim: The aim of this study was to validate a Chinese version of the painDETECT questionnaire (PD-Q) for the screening and assessment of neuropathic pain (NeP) in a Hong Kong Chinese population. Methods: The PD-Q was translated and cross-culturally adapted from the original German PD-Q, with forward and backward translation according to standard guidelines followed by cognitive debriefing, and finalized by an expert panel. A multicenter (6-site) observational study was conducted to evaluate the validity of the PD-Q. Patients aged 18 or above with medical conditions giving rise to either neuropathic or nociceptive pain (NoP) provided informed consent to participate in this study. Each patient was evaluated by at least two healthcare professionals for causes of pain, the visual analogue scale (VAS), numeric rating scale (NRS) and the PD-Q. Results: Hong Kong Chinese adults (n = 151) were given the clinical description of NeP (n = 93), NoP (n = 41), or mixed pain (n = 17). The mean age of study subjects was 58.5 years (age range: 26–90 years); 94 subjects (62.3%) were female. The mixed pain group was only analysed qualitatively, with validation based on the remaining 134 patients. Mean PD-Q scores for patients diagnosed with NeP and NoP were 19.9 [standard deviation (SD) = 6.4] and 12.5 (SD = 6.2) respectively. Receiver operating characteristic (ROC) curves were plotted for the upper/lower boundaries. The upper boundary was calculated on the basis of a neuropathic diagnosis and a nociceptive diagnosis. The cut-off point was > 18 (80% sensitivity, 60% specificity), and area under the ROC curve (AUC) was 0.67 (P < 0.001). The lower boundary was calculated on the basis of a nociceptive and a neuropathic diagnosis. The cut-off point was < 13 (90% sensitivity, 50% specificity), and AUC was 0.79 (P < 0.001). Conclusions: The PD-Q is a reliable and valid scale to determine neuropathic components of chronic pain in the Hong Kong Chinese population. Validation in a larger Chinese-speaking population worldwide is necessary.
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神经性疼痛筛查问卷painDETECT的中文验证和文化适应性研究
目的:本研究旨在验证用于筛查和评估香港华人神经病理性疼痛(NeP)的中文版 painDETECT 问卷 (PD-Q)。研究方法根据标准指南对 PD-Q 进行正向和反向翻译,然后进行认知汇报,最后由专家小组定稿。为评估 PD-Q 的有效性,我们开展了一项多中心(6 个研究地点)观察研究。年龄在 18 岁或 18 岁以上、患有神经性或痛觉性疼痛(NoP)的患者在知情同意的情况下参与了这项研究。每名患者至少由两名医护人员对疼痛原因、视觉模拟量表(VAS)、数字评分量表(NRS)和 PD-Q 进行评估。结果香港华裔成年人(n = 151)的临床描述为 NeP(n = 93)、NoP(n = 41)或混合痛(n = 17)。研究对象的平均年龄为 58.5 岁(年龄范围:26-90 岁);94 名研究对象(62.3%)为女性。混合疼痛组仅进行了定性分析,其余 134 名患者的情况进行了验证。被诊断为 NeP 和 NoP 患者的 PD-Q 平均得分分别为 19.9 [标准差 (SD) = 6.4] 和 12.5 (SD = 6.2)。绘制了上界/下界的接收者操作特征曲线(ROC)。上界根据神经病理性诊断和痛觉诊断计算得出。分界点大于 18(灵敏度为 80%,特异度为 60%),ROC 曲线下面积 (AUC) 为 0.67(P < 0.001)。下限是根据痛觉诊断和神经病理性诊断计算得出的。分界点小于 13(灵敏度为 90%,特异性为 50%),AUC 为 0.79(P < 0.001)。结论:PD-QPD-Q 是一种可靠有效的量表,可用于确定香港华裔人群慢性疼痛中的神经病理性成分。有必要在全球更多的华语人群中进行验证。
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