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The mNIHSS appears to be identical clinimetrically to the original NIHSS when the same data are used for validation and reliability. Power appears to be greater with the mNIHSS with the use of 24-hour end points, suggesting the need for fewer patients in trials designed to detect treatment effects comparable to rtPA. The mNIHSS contains fewer items and might be simpler to use in clinical research trials. Prospective analysis of reliability and validity, with the use of an independently collected cohort, must be obtained before the mNIHSS is used in a research setting.
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Patrick D. Lyden
University of Southern California
Mei Lü
Harvard University
Steven R. Levine
Vascular / Pulmonary Vascular
Stroke
Wayne State University
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Lyden et al. (Fri,) studied this question.
synapsesocial.com/papers/69d995405e5bcb4e3b837187 — DOI: https://doi.org/10.1161/01.str.32.6.1310