Volume 31, Issue 1 pp. 6-12

Infrared-monitored cold response in the assessment of Raynaud's phenomenon

J. Foerster

J. Foerster

Clinic for Dermatology and Internal Medicine with a focus on Rheumatology, Charité, Berlin, Germany

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S. Wittstock

S. Wittstock

Clinic for Dermatology and Internal Medicine with a focus on Rheumatology, Charité, Berlin, Germany

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S. Fleischanderl

S. Fleischanderl

Clinic for Dermatology and Internal Medicine with a focus on Rheumatology, Charité, Berlin, Germany

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A Storch

A Storch

Clinic for Dermatology and Internal Medicine with a focus on Rheumatology, Charité, Berlin, Germany

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G. Riemekasten

G. Riemekasten

Clinic for Dermatology and Internal Medicine with a focus on Rheumatology, Charité, Berlin, Germany

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O. Hochmuth

O. Hochmuth

Institute for Information, Humboldt University of Berlin, Berlin, Germany

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B Meffert

B Meffert

Institute for Information, Humboldt University of Berlin, Berlin, Germany

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H. Meffert

H. Meffert

Clinic for Dermatology and Internal Medicine with a focus on Rheumatology, Charité, Berlin, Germany

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M. Worm

M. Worm

Clinic for Dermatology and Internal Medicine with a focus on Rheumatology, Charité, Berlin, Germany

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First published: 31 October 2005
Citations: 23
Dr med. John Foerster, Klinik fuer Dermatologie und Allergologie, Charité Campus Mitte, Schumannstr. 20–21, 10117 Berlin.
Email: [email protected]

Conflict of interest: none declared.

The first two authors contributed equally to the manuscript.

Summary

Background. Evaluation of treatments for Raynaud's phenomenon (RP) requires objective response parameters in addition to clinical activity scores. Thermographic monitoring of fingertip re-warming after cold challenge has been widely used but usually requires sophisticated equipment. We have previously shown that fingertip re-warming after cold challenge follows a first-order transient response curve that can be described by a single variable, designated τ.

Objectives. Here, we describe a novel device termed a duosensor, which records the τ value upon cold challenge in an automated manner.

Methods. We determined τ values in healthy probands, patients with primary or secondary RP associated with autoimmune disease and patients with scleroderma-associated RP following cold challenge, to determine assay variability, sensitivity and specificity.

Results. Duosensor-based thermography exhibited low intraindividual variability in healthy probands. As expected, τ values in RP patients were significantly increased compared with controls (8.08 ± 3.65 min vs. 3.23 ± 1.65 min). The duosensor-determined τ value yielded a specificity of 94.6% and predictive value of 95.3% for the presence of RP in a retrospective analysis of 139 patients. Furthermore, in a cohort of scleroderma patients with RP, patient self-assessment of RP severity correlated with τ values.

Conclusions. Taken together, the present data suggest that τ value determination provides a suitable outcome measure for clinical studies of novel RP treatments. As the duosensor is a simple stand-alone device requiring no supporting equipment and minimal personnel attention, it should allow RP activity monitoring even in clinical settings with minimal technical infrastructure.

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