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Nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis

There is no clear understanding of the mechanisms causing persistent pain in patients with whiplash associated disorder (WAD). The aim of this systematic review was to assess the evidence for nerve pathology and neuropathic pain in patients with WAD. EMBASE, PubMed, CINAHL (EBSCO), and MEDLINE were...

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Autores principales: Fundaun, Joel, Kolski, Melissa, Baskozos, Georgios, Dilley, Andrew, Sterling, Michele, Schmid, Annina B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612893/
https://www.ncbi.nlm.nih.gov/pubmed/35050963
http://dx.doi.org/10.1097/j.pain.0000000000002509
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author Fundaun, Joel
Kolski, Melissa
Baskozos, Georgios
Dilley, Andrew
Sterling, Michele
Schmid, Annina B
author_facet Fundaun, Joel
Kolski, Melissa
Baskozos, Georgios
Dilley, Andrew
Sterling, Michele
Schmid, Annina B
author_sort Fundaun, Joel
collection PubMed
description There is no clear understanding of the mechanisms causing persistent pain in patients with whiplash associated disorder (WAD). The aim of this systematic review was to assess the evidence for nerve pathology and neuropathic pain in patients with WAD. EMBASE, PubMed, CINAHL (EBSCO), and MEDLINE were searched from inception to 1(st) September 2020. Study quality and risk of bias were assessed using the Newcastle-Ottawa Quality Assessment Scales. Fifty-four studies reporting on 390,644 patients and 918 controls were included. Clinical questionnaires suggested symptoms of predominant neuropathic characteristic in 34% of patients (range 25-75%). Mean prevalence of nerve pathology detected with neurological examination was 13% (0-100%) and 32% (10-100%) with electrodiagnostic testing. Patients independent of WAD severity (Quebec Task Force grades I-IV) demonstrated significantly impaired sensory detection thresholds of the index finger compared to controls, including mechanical (SMD 0.65 [0.30;1.00] p< 0.005), current (SMD 0.82 [0.25;1.39] p=0.0165), cold (SMD -0.43 [-0.73;-0.13] p=0.0204) and warm detection (SMD 0.84 [0.25;1.42] p=0.0200). Patients with WAD had significantly heightened nerve mechanosensitivity compared to controls upon median nerve pressure pain thresholds (SMD - 1.10 [-1.50;-0.70], p<0.0001) and neurodynamic tests (SMD 1.68 [0.92;2.44], p=0.0004). Similar sensory dysfunction and nerve mechanosensitivity was seen in WAD grade II, which contradicts its traditional definition of absent nerve involvement. Our findings strongly suggest a subset of patients with WAD demonstrate signs of peripheral nerve pathology and neuropathic pain. Although there was heterogeneity among some studies, typical WAD classifications may need to be reconsidered and include detailed clinical assessments for nerve integrity.
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spelling pubmed-76128932022-07-01 Nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis Fundaun, Joel Kolski, Melissa Baskozos, Georgios Dilley, Andrew Sterling, Michele Schmid, Annina B Pain Article There is no clear understanding of the mechanisms causing persistent pain in patients with whiplash associated disorder (WAD). The aim of this systematic review was to assess the evidence for nerve pathology and neuropathic pain in patients with WAD. EMBASE, PubMed, CINAHL (EBSCO), and MEDLINE were searched from inception to 1(st) September 2020. Study quality and risk of bias were assessed using the Newcastle-Ottawa Quality Assessment Scales. Fifty-four studies reporting on 390,644 patients and 918 controls were included. Clinical questionnaires suggested symptoms of predominant neuropathic characteristic in 34% of patients (range 25-75%). Mean prevalence of nerve pathology detected with neurological examination was 13% (0-100%) and 32% (10-100%) with electrodiagnostic testing. Patients independent of WAD severity (Quebec Task Force grades I-IV) demonstrated significantly impaired sensory detection thresholds of the index finger compared to controls, including mechanical (SMD 0.65 [0.30;1.00] p< 0.005), current (SMD 0.82 [0.25;1.39] p=0.0165), cold (SMD -0.43 [-0.73;-0.13] p=0.0204) and warm detection (SMD 0.84 [0.25;1.42] p=0.0200). Patients with WAD had significantly heightened nerve mechanosensitivity compared to controls upon median nerve pressure pain thresholds (SMD - 1.10 [-1.50;-0.70], p<0.0001) and neurodynamic tests (SMD 1.68 [0.92;2.44], p=0.0004). Similar sensory dysfunction and nerve mechanosensitivity was seen in WAD grade II, which contradicts its traditional definition of absent nerve involvement. Our findings strongly suggest a subset of patients with WAD demonstrate signs of peripheral nerve pathology and neuropathic pain. Although there was heterogeneity among some studies, typical WAD classifications may need to be reconsidered and include detailed clinical assessments for nerve integrity. 2022-07-01 2021-10-12 /pmc/articles/PMC7612893/ /pubmed/35050963 http://dx.doi.org/10.1097/j.pain.0000000000002509 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license.
spellingShingle Article
Fundaun, Joel
Kolski, Melissa
Baskozos, Georgios
Dilley, Andrew
Sterling, Michele
Schmid, Annina B
Nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis
title Nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis
title_full Nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis
title_fullStr Nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis
title_full_unstemmed Nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis
title_short Nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis
title_sort nerve pathology and neuropathic pain after whiplash injury: a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612893/
https://www.ncbi.nlm.nih.gov/pubmed/35050963
http://dx.doi.org/10.1097/j.pain.0000000000002509
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