The significance of crossovers after randomization in the STICH trial

17Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Introduction Of all forms of stroke, spontaneous intracerebral haemorrhage (ICH) causes the highest morbidity and mortality. The Surgical Trial in Intracerebral Haemorrhage (STICH) found no difference in outcomes between patients randomized to surgical or conservative treatment. Patients and methods Of 530 patients randomized to initial conservative treatment, 140 crossed over to surgery. This study examines the variables associated with crossover. Results Dominant features of the crossover group were: male, (p = 0.04), right-sided clot (p = 0.03), lobar clot (p = 0.003), clot volume (median 64 mL for crossovers vs. 38 mL for others, p < 0.00001), midline shift (median 6 mm for crossovers vs. 3 mm for others, p > 0.00001), superficial clot (median 1.3 mm for cross-overs vs. 11.5 mm for others, p < 0.00001), and randomization within 12 hours of ictus (p < 0.0005). Thalamic location (p = 0.002) was under-represented. Intraventricular haemorrhage, hydrocephalus, and focal deficits were not associated with crossover. Craniotomy was the method of evacuation in 85% of crossover patients. Conclusions Crossover to surgery was more likely when ICH had these features: Right side, lobar location, superficial, large volume, big shift, and early randomization. Crossovers formed a worse prognostic group compared to non-crossovers. Surgery did not affect trial results, which were analyzed by intention-to-treat. © 2006 Springer-Verlag.

Cite

CITATION STYLE

APA

Prasad, K. S. M., Gregson, B. A., Bhattathiri, P. S., Mitchell, P., & Mendelow, A. D. (2006). The significance of crossovers after randomization in the STICH trial. Acta Neurochirurgica, Supplementum, (96), 61–64. https://doi.org/10.1007/3-211-30714-1_15

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free