Key result
Female sex was associated with comparable functional outcomes to male sex after ischemic stroke (OR 0.96; 95% CI 0.85-1.06), and both sexes showed a similar response to r-tPA.
Why the study?
Does sex influence the functional outcome and response to intravenous r-tPA in patients with ischemic stroke?
Observational (n=4,575)
Yes
Does sex influence the functional outcome and response to intravenous r-tPA in patients with ischemic stroke?
Answers are grounded in this paper and cite their sources.
Functional outcomes and response to r-tPA after ischemic stroke are similar between sexes, though a nonlinear age-by-sex interaction suggests worse outcomes for females over 45 years.
Background and Purpose— We hypothesized that any sex-related difference in outcome poststroke is explained by other prognostic factors and that the response to intravenous recombinant tissue-type plasminogen activator (r-tPA) is equal in males and females after adjustment for such factors. Methods— We accessed an independent collection of randomized clinical trials—the VISTA (Virtual International Stroke Trials Archive). Data were preprocessed by selecting complete cases (n=8028) and matching females to males (coarsened exact matching, n=4575, 24.3% r-tPA). Outcome was assessed by the 7-point modified Rankin Scale (mRS) measured at 90 days after ischemic stroke. Relationship among variables was estimated by adjusted regression analysis. Results— In nonthrombolyzed patients, ordinal analysis of mRS adjusting for stroke- and sex-related prognostic factors suggested comparable outcomes for females and males (odds ratio, 0.96; 95% confidence interval, 0.85–1.06). Females responded comparably to r-tPA as did males, irrespective of the outcome definition of mRS (ordinal: P Interaction =0.46, relative excess risk because of interaction=0). The number needed to treat was 6.8 and 11.2 for 1 female to achieve mRS score of 0 to 2 and 0 to 1, which was highly congruent with males. Analysis for a nonlinear variation of age-by-sex revealed a good outcome for females <45 years with significant disadvantage thereafter (mRS score of 0–2: P Interaction =0.004). No relationship between sex, r-tPA, and bleeding complications was evident. Conclusions— Functional outcome (mRS) without r-tPA was overall similar between the sexes, as was the response to r-tPA. Nonlinear sex-by-age interaction improved estimates of functional independence; this should be considered in sex-related studies in stroke.
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Hametner et al. (2016) conducted an observational in Ischemic stroke (n=4,575). Female sex vs. Male sex was evaluated on 7-point modified Rankin Scale (mRS) at 90 days (OR 0.96, 95% CI 0.85-1.06). Female sex was associated with comparable functional outcomes to male sex after ischemic stroke (OR 0.96; 95% CI 0.85-1.06), and both sexes showed a similar response to r-tPA.
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