2014
DOI: 10.1007/s00296-014-3191-z
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Development of a bedside pain assessment kit for the classification of patients with osteoarthritis

Abstract: There are no standardized bedside assessments for subtyping patients with osteoarthritis (OA) based on pain mechanisms. Thus, we developed a bedside sensory testing kit (BSTK) to classify OA patients based on sensory profiles potentially indicative of pain mechanism. After usability and informal reliability testing (n = 22), the kit was tested in a formal reliability study (n = 20). Patients completed questionnaires and sensory testing: pressure algometry to detect hyperalgesia; repeat algometry after heteroto… Show more

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Cited by 29 publications
(31 citation statements)
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“…Pressure algometry can assess pressure pain sensitivity, and metal rods that are heated or cooled can assess thermal sensitivity. Some evidence supports the reliability and validity of this approach 62 ; therefore, bedside QST may provide an important next step in mechanism-based pain assessment. 27 …”
Section: Assessment Of Pain Mechanismsmentioning
confidence: 94%
“…Pressure algometry can assess pressure pain sensitivity, and metal rods that are heated or cooled can assess thermal sensitivity. Some evidence supports the reliability and validity of this approach 62 ; therefore, bedside QST may provide an important next step in mechanism-based pain assessment. 27 …”
Section: Assessment Of Pain Mechanismsmentioning
confidence: 94%
“…1,2 Osteoarthritis of the knee has a prevalence of over 250 million people globally. 3 It is anticipated that this number will rise sharply in the future due to rapidly growing, ageing populations paralleled with the increasing prevalence of obesity.…”
Section: Introductionmentioning
confidence: 99%
“…Evidence supports that pain perception differs among ethnic populations . In this review, only 5 studies reported the ethnicity of their participants . Of these studies, Lundlad et al .…”
Section: Discussionmentioning
confidence: 92%
“…The time intervals between successive sessions ranged from 2 minutes to 10 days for test‐retest reliability, 2 minutes to 10 days for intrarater reliability, and 5 to 30 minutes for interrater reliability. The number of trials ranged from 2 to 4 for PPT measurements, except for one study that conducted only 1 trial and one study that did not report the number of trials . For studies that conducted more than 1 trial, only 4 studies reported rest periods; these ranged from 20 seconds to 1 minute between trials …”
Section: Resultsmentioning
confidence: 99%
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