Can self-reported pain characteristics and bedside test be used for the assessment of pain mechanisms? An analysis of results of neuropathic pain questionnaires and quantitative sensory testing.


Journal

Pain
ISSN: 1872-6623
Titre abrégé: Pain
Pays: United States
ID NLM: 7508686

Informations de publication

Date de publication:
09 2019
Historique:
pubmed: 5 6 2019
medline: 28 7 2020
entrez: 5 6 2019
Statut: ppublish

Résumé

Hyperalgesia and allodynia are frequent in neuropathic pain. Some pain questionnaires such as the Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) and the Neuropathic Pain Scale (NPS) include self-assessment or bedside testing of hyperalgesia/allodynia. The aim of this study was to determine to what extent LANSS and NPS data are congruent with findings on quantitative sensory testing (QST). Self-reported presence of dynamic mechanical allodynia (DMA) and descriptors of hot, cold, or deep ongoing pain (the NPS and LANSS) as well as bedside findings of mechanical allodynia (LANSS) were compared with signs of DMA and thermal hyperalgesia on QST in 617 patients with neuropathic pain. Self-reported abnormal skin sensitivity (LANSS) showed a moderate concordance with DMA during bedside test (67.9%, κ = 0.391) or QST (52.8%, κ = 0.165). Receiver operating curve analysis for self-reported DMA yielded similar area-under-the-curve values for the LANSS (0.65, confidence interval: 0.59%-0.97%) and NPS (0.71, confidence interval: 0.66%-0.75%) with high sensitivity but low specificity. Self-reported deep pain intensity was higher in patients with blunt pressure hyperalgesia, but not in patients with DMA or thermal hyperalgesia. No correlations were observed between self-reported hot or cold pain quality and thermal hyperalgesia on QST. Self-reported abnormal skin sensitivity has a high sensitivity to identify patients with DMA, but its low specificity indicates that many patients mean something other than DMA when reporting this symptom. Self-reported deep pain is related to deep-tissue hypersensitivity, but thermal qualities of ongoing pain are not related to thermal hyperalgesia. Questionnaires mostly evaluate the ongoing pain experience, whereas QST mirrors sensory functions. Therefore, both methods are complementary for pain assessment.

Identifiants

pubmed: 31162335
doi: 10.1097/j.pain.0000000000001601
pii: 00006396-201909000-00019
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2093-2104

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Auteurs

Janne Gierthmühlen (J)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

Ulrike Schneider (U)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

Martina Seemann (M)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

Sandra Freitag-Wolf (S)

Institut of Medical Informatics and Statistics, University of Kiel, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

Christian Maihöfner (C)

Department of Neurology, General Hospital Fürth, Fürth, Germany.

Elena K Enax-Krumova (EK)

Departments of Pain Management and.
Neurology, BG University Hospital Bergmannsheil gGmbH, Ruhr-University Bochum, Bochum, Germany.

Shahnaz-C Azad (SC)

Department of Anesthesiology, University Hospital Munich, Campus Groβhadern, Munich, Germany.

Nurcan Üçeyler (N)

Department of Neurology, University of Würzburg, Würzburg, Germany.

Frank Birklein (F)

Department of Neurology, University Medical Centre Mainz, Mainz, Germany.

Christoph Maier (C)

Departments of Pain Management and.

Thomas Tölle (T)

Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Rolf-Detlef Treede (RD)

Chair of Neurophysiology, Center of Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.

Ralf Baron (R)

Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

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