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

Author:

Leung Howan1,Ip Josephine W.Y.2,Lam Joseph M.K.3,Lee Gavin K.W.4,Li Carina C.F.5,Li Richard6ORCID,Mok Vincent1,Tsoi Tak H.7,Wong Chun P.3,Wong Steven H.S.8,Chang Chun M.5,Freynhagen Rainer9ORCID

Affiliation:

1. Department of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong, China

2. Department of Orthopaedics and Traumatology, The University of Hong Kong, Hong Kong, China

3. Private Practice, Hong Kong, China

4. Rheumatology Centre, Hong Kong Sanatorium and Hospital, Hong Kong, China

5. Department of Anaesthesia and Intensive Care, Tuen Mun Hospital, Hong Kong, China

6. Department of Medicine, Pamela Youde Nethersole Eastern Hospital, Hong Kong, China

7. Neurology Centre, Hong Kong Sanatorium and Hospital, Hong Kong, China

8. Department of Anaesthesiology and Operating Theatre Services, Queen Elizabeth Hospital, Hong Kong, China

9. Department of Anaesthesiology, Critical Care Medicine, Pain Medicine, Pain Center Lake Starnberg, Benedictus Hospital Feldafing, 82340 Feldafing, Germany; Clinic for Anesthesiology, Klinikum rechts der Isar, Technische Universität München, 81675 Munich, Germany

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.

Funder

Pfizer Hong Kong

Publisher

Open Exploration Publishing

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