Validation and usability of modified palmoplantar psoriasis area and severity index in patients with palmoplantar psoriasis: A prospective longitudinal cohort study

Author:

Nagendran Adithya1,Hanumanthu Vinod2,Dogra Sunil2,Narang Tarun2,Venkata Maha Pinnaka Lakshmi3

Affiliation:

1. Department of Dermatology Venereology and Leprology, SS Institute of Medical Sciences and Research centre, Davanagere, Karnataka, India

2. Department of Dermatology Venereology and Leprology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India

3. Department of Community Medicine & School of Public Health, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India

Abstract

Background Palmoplantar psoriasis (PPP), a troublesome variant, does not have any validated scoring system to assess disease severity. Objective To validate modified Palmoplantar Psoriasis Area and Severity Index (m-PPPASI) in patients affected with PPP and to categorise it based on Dermatology Life Quality Index (DLQI). Methods In this prospective study, patients with PPP aged > 18 years visiting the psoriasis clinic at a tertiary care centre were included and requested to complete DLQI during each visit at baseline, 2nd week, 6th and 12th week. m-PPPASI was used by the raters to determine the disease severity. Results Overall, 73 patients were included. m-PPPASI demonstrated high internal consistency (α = 0.99), test-retest reliability of all three raters, that is, Adithya Nagendran (AN) (r = 0.99, p < 0.0001), Tarun Narang (TN) (r = 1.0, p < 0.0001) and Sunil Dogra (SD) (r = 1.0, p < 0.0001) and inter-rater agreement (intra-class correlation coefficient = 0.83). Face and content validity index for items I-CVI = 0.845 were robust, and the instrument was uniformly rated as easy to use (Likert scale 2) by all three raters. It was found to be responsive to change (r = 0.92, p < 0.0001). Minimal clinically important differences (MCID)-1 and MCID-2 calculated by receiver operating characteristic curve using DLQI as anchor were 2 and 35%, respectively. DLQI equivalent cutoff points for m-PPPASI were 0–5 for mild, 6–9 for moderate, 10–19 for severe, and 20–72 for very severe disease. Limitation Small sample size and single-center validation were the major limitations. m-PPPASI doesn’t objectively measure all characteristics of PPP such as “fissuring” and “scaling” which could also be taken into consideration. Conclusion m-PPPASI is validated in PPP and can be readily utilized by physicians. However, further large-scale studies are needed.

Publisher

Scientific Scholar

Subject

Infectious Diseases,Dermatology

Reference26 articles.

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2. Clinical profile of psoriasis in North India;Bedi;Indian J Dermatol Venereol Leprol,1995

3. Natural history of psoriasis: a study from the Indian subcontinent;Kaur;J Dermatol,1997

4. Epidemiological pattern of psoriasis, vitiligo and atopic dermatitis in India: Hospital-based point prevalence;Kumar;Indian Dermatol Online J,2014

5. Psoriasis in the tropics: an epidemiological survey;Okhandiar;J Indian Med Assoc,1963

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