Article Text

Download PDFPDF

Association between quantitative sensory testing and pain or disability in paediatric chronic pain: protocol for a systematic review and meta-analysis
  1. Daniel Eric Schoth1,
  2. Markus Blankenburg2,
  3. Julia Wager3,
  4. Philippa Broadbent1,
  5. Jin Zhang1,
  6. Boris Zernikow3,
  7. Christina Liossi1,4
  1. 1 School of Psychology, University of Southampton, Southampton, UK
  2. 2 Faculty of Health, University of Witten/Herdecke, Witten, Germany
  3. 3 Universitat Witten/Herdecke, Witten, Germany
  4. 4 Paediatric Psychology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK
  1. Correspondence to Professor Christina Liossi; C.Liossi{at}soton.ac.uk

Abstract

Introduction This protocol describes the objective and methods of a systematic review of the association between quantitative sensory testing (QST) measures and pain intensity or disability in paediatric chronic pain (PCP). The review will also assess whether the relationship strength is moderated by variables related to the QST method and pain condition; the use of QST in PCP (modalities, outcome measures and anatomical test sites as well as differentiating between pain mechanisms (eg, neuropathic vs nociceptive) and in selecting analgesics); the reliability of QST across the paediatric age range; the ability of QST to differentiate patients with chronic pain from healthy controls; and differences between anatomical test sites.

Methods and analysis Medline, PsycINFO, CINHAL, Web of Science, Scopus, Cochrane Library and OpenGrey will be searched. English language studies will be eligible if they recruit a sample aged 6–24 (inclusive) with chronic pain, including primary and secondary pain; apply at least one of the following QST modalities: chemical, electrical, mechanical (subgroups include pressure, punctate/brush and vibratory) or thermal stimulus to measure perception of noxious or innocuous stimuli applied to skin, muscle or joint; use a testing protocol to control for stimulus properties: modality, anatomical site, intensity, duration and sequence. Following title and abstract screening, the full texts of relevant records will be independently assessed by two reviewers. For eligible studies, one reviewer will extract study characteristics and data, and another will check for accuracy. Both will undertake independent quality assessments using the Appraisal Tool for Cross-Sectional Studies. A qualitative synthesis will be presented with discussion centred around different QST modalities. Where eligible data permit, meta-analyses will be performed separately for different QST modalities using comprehensive meta-analysis.

Ethics and dissemination Review findings will be reported in a peer-reviewed journal and presented at conferences. The study raises no ethical issues.

PROSPERO registration number CRD42019134069.

  • quantitative sensory testing
  • QST
  • pediatric chronic pain
  • disability
  • systematic review
  • meta-analysis

This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Footnotes

  • Contributors CL conceived the idea, planned and designed the study protocol. CL and DES planned the data extraction and statistical analysis and wrote the first draft; MB, JW, BZ, JZ and PB provided critical insights. All authors have approved and contributed to the final written manuscript.

  • Funding This development of this protocol was supported by ESRC (Grant number: RES-000-22-4128). This funding source had no role in the design of this review and will not have any role during its execution, analyses, interpretation of the data or decision to submit results.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.