Abstract

ObjectiveValid, reliable, and clinically relevant outcome measures are necessary in clinical studies of snake envenomation. The aim of this study was to evaluate the psychometric (validity and reliability) and clinimetric (minimal clinically important difference [MCID]) properties of the Patient-Specific Functional Scale (PSFS) in snakebite envenomation.MethodsWe performed a secondary analysis of two existing snakebite trials that measured clinical outcomes using the PSFS as well as other quality of life and functional assessments. Data were collected at 3, 7, 10, and 17 days. Reliability was determined using Cronbach’s alpha for internal consistency and the intraclass correlation coefficient (ICC) for temporal stability at 10 and 17 days. Validity was assessed using concurrent validity correlating with the other assessments. The MCID was evaluated using the following criteria: (1) the distribution of stable patients according to both standard error of measurement (SEM) and responsiveness techniques, and (2) anchor-based methods to compare between individuals and to detect discriminant ability of a positive change with a receiver operator characteristic (ROC) curve and optimal cutoff point.ResultsA total of 86 patients were evaluated in this study. The average PSFS scores were 5.37 (SD 3.23), 7.95 (SD 2.22), and 9.12 (SD 1.37) at 3, 7, and 10 days, respectively. Negligible floor effect was observed (maximum of 8% at 3 days); however, a ceiling effect was observed at 17 days (25%). The PSFS showed good reliability with an internal consistency of 0.91 (Cronbach’s alpha) (95% CI 0.88, 0.95) and a temporal stability of 0.83 (ICC) (95% CI 0.72, 0.89). The PSFS showed a strong positive correlation with quality of life and functional assessments. The MCID was approximately 1.0 for all methods.ConclusionsWith an MCID of approximately 1 point, the PSFS is a valid and reliable tool to assess quality of life and functionality in patients with snake envenomation.

Highlights

  • The Patient-Specific Functional Scale (PSFS) showed good reliability with an internal consistency of 0.91 (Cronbach’s alpha) and a temporal stability of 0.83 (ICC)

  • The PSFS has been widely used with other clinical populations; to date, no previous study has evaluated the reliability, temporal stability, and minimally clinically important difference (MCID) of the PSFS in patients with snake envenomation

  • Our results demonstrate that the PSFS is reliable, stable over time, externally valid, and strongly correlated with extremity functional assessment and other indicators of quality of life

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Summary

Introduction

Snake envenomation is a common public health problem worldwide with annual estimates ranging from 421,000 to 1,842,000 cases per year, with 20,000 to 94,000 deaths per year.[1,2,3] The burden of disease is pronounced in low- and middle-income countries, and has been reclassified as a neglected tropical disease by the World Health Organization, leading to further interest in the field.[2, 4, 5] Potential new therapies are being developed that will require clinical trials.[6,7,8,9] the existing literature lacks data regarding patient-centered outcome measures for use in snake envenomation clinical trials.[10] prior trials have primarily used diagnosis-oriented endpoints, such as surrogate markers of coagulopathy, as primary outcomes.[11,12,13,14,15] Outcome measures that are patient centered and ideally patient reported will yield the most informative and clinically relevant information from the clinical trials evaluating potential snake envenomation therapies.[16]

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