Reliability of the English version of the painDETECT questionnaire

Background: The painDETECT questionnaire (PD-Q) has been used widely for the identification of neuropathic pain (NeP); however, the reliability of the English version of the PD-Q has never been investigated. Objective: This study aimed to determine the reliability of the PD-Q pre- (T0) and immediate...

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Main Authors: Tampin, B., Bohne, T., Callan, M., Kvia, M., Melsom Myhre, A., Neoh, E., Bharat, C., Slater, Helen
Format: Journal Article
Published: Librapharm 2017
Online Access:http://hdl.handle.net/20.500.11937/51245
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author Tampin, B.
Bohne, T.
Callan, M.
Kvia, M.
Melsom Myhre, A.
Neoh, E.
Bharat, C.
Slater, Helen
author_facet Tampin, B.
Bohne, T.
Callan, M.
Kvia, M.
Melsom Myhre, A.
Neoh, E.
Bharat, C.
Slater, Helen
author_sort Tampin, B.
building Curtin Institutional Repository
collection Online Access
description Background: The painDETECT questionnaire (PD-Q) has been used widely for the identification of neuropathic pain (NeP); however, the reliability of the English version of the PD-Q has never been investigated. Objective: This study aimed to determine the reliability of the PD-Q pre- (T0) and immediately post- (T1) clinical consultation and at one-week follow-up (T2). Methods: We recruited 157 patients attending a Neurosurgery Spinal Clinic and Pain Management Department. Minor changes to PD-Q instructions were made to facilitate patient understanding; however, no changes to individual items or scoring were made. Intraclass correlation coefficients (ICCs) were used to assess the reliability of PD-Q total scores between T0–T1 and T0–T2; weighted kappa (κ) was used to assess the agreement of PD-Q classifications (unlikely NeP, ambiguous, likely NeP) between all time-points. To ensure stability of clinical pain, patients scoring ≤2 or ≥6 on the Patient Global Impression Scale (PGIC) at T2 were excluded from the T0–T2 analysis. Results: Accounting for missing data and exclusions (change in PGIC score), data for 136 individuals (mean [SD] age: 56.8 [15.2]; 54% male) was available, of whom n = 129 were included in the T0–T1 and n = 69 in the T0–T2 comparisons. There was almost perfect agreement between the PD-Q total scores at T0–T1 time-points (ICC 0.911; 95% CI: 0.882–0.941) and substantial agreement at T0–T2 (ICC 0.792; 95% CI: 0.703–0.880). PD-Q classifications demonstrated substantial agreement for T0–T1 (weighted κ: 0.771; 95% CI: 0.683–0.858) and for T0–T2 (weighted κ: 0.691; 95% CI: 0.553–0.830). Missing data was accounted in 13% of our cohort and over 42% of our patients drew multiple pain areas on the PD-Q body chart. Conclusion: The English version of the PD-Q is reliable as a screening tool for NeP. The validity of the questionnaire is still in question and has to be investigated in future studies.
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spelling curtin-20.500.11937-512452017-09-13T15:48:51Z Reliability of the English version of the painDETECT questionnaire Tampin, B. Bohne, T. Callan, M. Kvia, M. Melsom Myhre, A. Neoh, E. Bharat, C. Slater, Helen Background: The painDETECT questionnaire (PD-Q) has been used widely for the identification of neuropathic pain (NeP); however, the reliability of the English version of the PD-Q has never been investigated. Objective: This study aimed to determine the reliability of the PD-Q pre- (T0) and immediately post- (T1) clinical consultation and at one-week follow-up (T2). Methods: We recruited 157 patients attending a Neurosurgery Spinal Clinic and Pain Management Department. Minor changes to PD-Q instructions were made to facilitate patient understanding; however, no changes to individual items or scoring were made. Intraclass correlation coefficients (ICCs) were used to assess the reliability of PD-Q total scores between T0–T1 and T0–T2; weighted kappa (κ) was used to assess the agreement of PD-Q classifications (unlikely NeP, ambiguous, likely NeP) between all time-points. To ensure stability of clinical pain, patients scoring ≤2 or ≥6 on the Patient Global Impression Scale (PGIC) at T2 were excluded from the T0–T2 analysis. Results: Accounting for missing data and exclusions (change in PGIC score), data for 136 individuals (mean [SD] age: 56.8 [15.2]; 54% male) was available, of whom n = 129 were included in the T0–T1 and n = 69 in the T0–T2 comparisons. There was almost perfect agreement between the PD-Q total scores at T0–T1 time-points (ICC 0.911; 95% CI: 0.882–0.941) and substantial agreement at T0–T2 (ICC 0.792; 95% CI: 0.703–0.880). PD-Q classifications demonstrated substantial agreement for T0–T1 (weighted κ: 0.771; 95% CI: 0.683–0.858) and for T0–T2 (weighted κ: 0.691; 95% CI: 0.553–0.830). Missing data was accounted in 13% of our cohort and over 42% of our patients drew multiple pain areas on the PD-Q body chart. Conclusion: The English version of the PD-Q is reliable as a screening tool for NeP. The validity of the questionnaire is still in question and has to be investigated in future studies. 2017 Journal Article http://hdl.handle.net/20.500.11937/51245 10.1080/03007995.2017.1278682 Librapharm restricted
spellingShingle Tampin, B.
Bohne, T.
Callan, M.
Kvia, M.
Melsom Myhre, A.
Neoh, E.
Bharat, C.
Slater, Helen
Reliability of the English version of the painDETECT questionnaire
title Reliability of the English version of the painDETECT questionnaire
title_full Reliability of the English version of the painDETECT questionnaire
title_fullStr Reliability of the English version of the painDETECT questionnaire
title_full_unstemmed Reliability of the English version of the painDETECT questionnaire
title_short Reliability of the English version of the painDETECT questionnaire
title_sort reliability of the english version of the paindetect questionnaire
url http://hdl.handle.net/20.500.11937/51245