학술논문

Maximum intravenous alteplase dose for obese stroke patients is not associated with greater likelihood of worse outcomes.
Document Type
Article
Source
Thrombosis Research. Aug2021, Vol. 204, p76-80. 5p.
Subject
*ISCHEMIC stroke
*STROKE patients
*ALTEPLASE
*CHI-squared test
*LOGISTIC regression analysis
Language
ISSN
0049-3848
Abstract
IV alteplase is a primary treatment for acute ischemic stroke (AIS) at a weight-based dose (WBD) of 0.9 mg/kg and maximum dose (MD) of 90 mg. There are conflicting data regarding outcomes for those weighing ≥100 kg. There is also a paucity of data in Hispanics. The prevalence of adult obesity in the US has progressively increased; hence, the percentage of patients receiving the maximum dose also is expected to rise. We examined differences between patients treated with WBD vs. MD. A retrospective review of our center's Get With The Guidelines-Stroke database was performed for IV alteplase cases between October 2013–February 2017. Selection criteria included age ≥18 years, IV alteplase administration, and a recorded measured weight. Patients were dichotomized into WBD group weighing <100 kg and MD group weighing ≥100 kg. Categorical variables were analyzed using Chi square tests and continuous variables were analyzed using independent samples t -tests. Multivariable logistic regression analysis was performed to determine whether MD in combination with other variables was associated with poor outcomes. There were 328 patients included in the study, 38 (11.6%) received MD. Proportions of younger, male, and non-Hispanic were higher in the MD group. There were no statistically significant differences for initial NIHSS, discharge modified Rankin Scale (mRS), 90-day mRS, symptomatic intracerebral hemorrhage (sICH), or systemic hemorrhage between groups. One in ten patients thrombolysed for the treatment of AIS received MD. In a predominantly Hispanic population, those who received MD and WBD had similar rates of sICH, discharge disposition, and functional outcome (mRS) at discharge and at 90 days. Limitations include small sample size and attrition for the 90-day mRS. • One in ten patients receiving alteplase weighed at least 100 kg (MD group). • Max dose did not affect complications or discharge disposition vs weight-based dose. • No effect of max vs weight-based dose on discharge or 90-day modified Rankin Scale. • This study corroborates previous findings now in a primarily Hispanic population. [ABSTRACT FROM AUTHOR]