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Ann Rheum Dis. Published Online First: 17 September 2009. doi:10.1136/ard.2009.114843
Copyright © 2009 BMJ Publishing Group Ltd & European League Against Rheumatism.

Concise report

High frequency ultrasound measurement of digital dermal thickness in systemic sclerosis

Olga Kaloudi1,*, Francesca Bandinelli1, Emilio Filippucci2, Maria Letizia Conforti1, Irene Miniati1, Serena Guiducci1, Francesco Porta1, Antonio Candelieri3, Domenico Conforti3, Genesio Grassiri4, Walter Grassi2, Marco Matucci Cerinic1

1 Department of Biomedicine,Division of Rheumatology AOUC, Centre Denothe, University of Florence, Italy;
2 Division of Rheumatology, University of Marche, Jesi, Ancona, Italy;
3 Laboratory of Decision Engineering for Health Care Delivery,University of Calabria, Cosenza, Italy;
4 Esaote spa, Italy

Correspondence to: olga kaloudi, Department of Biomedicine,Division of Rheumatology AOUC, Centre Denothe, University of Florence, Flo, Villa Monna Tessa, Viale Pieraccini 18, Florence, 50139, Italy; olgakaloudi{at}hotmail.com

Accepted 17 August 2009

ABSTRACT

Background: Currently, the assessment of dermal thickness in Systemic Sclerosis (SSc) is performed by palpation with the modified Rodnan Skin Score (mRSS).

Objective: To verify if high frequency ultrasound (US) may be a reliable and a reproducible method to measure digital dermal thickness.

Methods: In 70 SSc patients, skin thickness was evaluated with US by two observers in two different sites of the second digit of the dominant limb to determine the inter-observer variability. Patients and controls were examined twice by the first observer for intra-observer variability. Patients were divided into three subgroups according to the phase of the disease (oedematous, fibrotic and atrophic).

Results: At both examined areas, US showed a significant dermal thickening (p<0,001) in the whole group of SSc patients. A low intra- and inter-observer variability was found. A highly significant correlation between the global mRSS and the local dermal thickness at the two examined sites (p:0.032 and p:0.021) was detected. Skin thickness resulted significantly higher in the oedematous than in the fibrotic group (p<0.001) and significantly higher in the fibrotic and the oedematous group (p<0.001) than in the atrophic group (p<0.002).

Conclusions: US is a reliable and reproducible tool, able to detect digital dermal thickening in SSc.


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