Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2014 Feb;134(2):351-358.
doi: 10.1038/jid.2013.318. Epub 2013 Jul 29.

Responsiveness to change and interpretability of the simplified psoriasis index

Affiliations
Free article
Clinical Trial

Responsiveness to change and interpretability of the simplified psoriasis index

Leena Chularojanamontri et al. J Invest Dermatol. 2014 Feb.
Free article

Abstract

The Simplified Psoriasis Index (SPI) is a summary measure of psoriasis with separate components for current severity (weighted for functionally or psychosocially important sites), psychosocial impact, and past behavior. The current severity components of the professionally assessed SPI (proSPI-s) and self-assessed SPI (saSPI-s) have each been shown to be valid and reliable. Their responsiveness to change and equivalence to the current standard (Psoriasis Area and Severity Index, PASI) were investigated. Responsiveness and minimum clinically important differences (MCIDs) were derived from PASI changes from baseline at weeks 4 (n=100) and 10 (n=65) in patients commencing therapy for psoriasis. Receiver operating characteristic (ROC) analysis confirmed that both measures detected responsiveness well (area under the curve (AUC)=0.72-0.96). On ROC and PASI-based anchor analysis, MCIDs equated to mean absolute and percentage changes of 5 and 60% (proSPI-s), and 7 and 70% (saSPI-s). Satisfactory response as defined by 75% reduction in PASI equated to 85 and 95% reductions in proSPI-s and saSPI-s, respectively. PASI-equivalent cutoff scores for mild (PASI<10) and severe (PASI>20) psoriasis were <9 and >18 for proSPI-s (n=300) and <10 and >20 for saSPI-s (n=200; AUC=0.86-0.96). These studies further support the validity of SPI for use in routine clinical practice.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Clin Epidemiol. 2008 Feb;61(2):102-9 - PubMed
    1. J Clin Epidemiol. 2010 Jan;63(1):28-36 - PubMed
    1. J Invest Dermatol. 2013 Aug;133(8):1956-62 - PubMed
    1. Arch Dermatol. 2011 Jan;147(1):95-8 - PubMed
    1. Lancet. 2005 Oct 15-21;366(9494):1367-74 - PubMed

LinkOut - more resources