Association Between Thrombolytic Door-to-Needle Time and 1-Year Mortality and Readmission in Patients With Acute Ischemic Stroke.

Abstract

Importance:Earlier administration of intravenous tissue plasminogen activator (tPA) in acute ischemic stroke is associated with reduced mortality by the time of hospital discharge and better functional outcomes at 3 months. However, it remains unclear whether shorter door-to-needle times translate into better long-term outcomes. Objective:To examine whether shorter door-to-needle times with intravenous tPA for acute ischemic stroke are associated with improved long-term outcomes. Design, Setting, and Participants:This retrospective cohort study included Medicare beneficiaries aged 65 years or older who were treated for acute ischemic stroke with intravenous tPA within 4.5 hours from the time they were last known to be well at Get With The Guidelines-Stroke participating hospitals between January 1, 2006, and December 31, 2016, with 1-year follow-up through December 31, 2017. Exposures:Door-to-needle times for intravenous tPA. Main Outcomes and Measures:The primary outcomes were 1-year all-cause mortality, all-cause readmission, and the composite of all-cause mortality or readmission. Results:Among the 61 426 patients treated with tPA within 4.5 hours, the median age was 80 years and 43.5% were male. The median door-to-needle time was 65 minutes (interquartile range, 49-88 minutes). The 48 666 patients (79.2%) who were treated with tPA and had door-to-needle times of longer than 45 minutes, compared with those treated within 45 minutes, had significantly higher all-cause mortality (35.0% vs 30.8%, respectively; adjusted HR, 1.13 [95% CI, 1.09-1.18]), higher all-cause readmission (40.8% vs 38.4%; adjusted HR, 1.08 [95% CI, 1.05-1.12]), and higher all-cause mortality or readmission (56.0% vs 52.1%; adjusted HR, 1.09 [95% CI, 1.06-1.12]). The 34 367 patients (55.9%) who were treated with tPA and had door-to-needle times of longer than 60 minutes, compared with those treated within 60 minutes, had significantly higher all-cause mortality (35.8% vs 32.1%, respectively; adjusted hazard ratio [HR], 1.11 [95% CI, 1.07-1.14]), higher all-cause readmission (41.3% vs 39.1%; adjusted HR, 1.07 [95% CI, 1.04-1.10]), and higher all-cause mortality or readmission (56.8% vs 53.1%; adjusted HR, 1.08 [95% CI, 1.05-1.10]). Every 15-minute increase in door-to-needle times was significantly associated with higher all-cause mortality (adjusted HR, 1.04 [95% CI, 1.02-1.05]) within 90 minutes after hospital arrival, but not after 90 minutes (adjusted HR, 1.01 [95% CI, 0.99-1.03]), higher all-cause readmission (adjusted HR, 1.02; 95% CI, 1.01-1.03), and higher all-cause mortality or readmission (adjusted HR, 1.02 [95% CI, 1.01-1.03]). Conclusions and Relevance:Among patients aged 65 years or older with acute ischemic stroke who were treated with tissue plasminogen activator, shorter door-to-needle times were associated with lower all-cause mortality and lower all-cause readmission at 1 year. These findings support efforts to shorten time to thrombolytic therapy.

Department

Description

Provenance

Subjects

Humans, Brain Ischemia, Tissue Plasminogen Activator, Fibrinolytic Agents, Thrombolytic Therapy, Patient Readmission, Infusions, Intravenous, Incidence, Cause of Death, Proportional Hazards Models, Retrospective Studies, Follow-Up Studies, Aged, Aged, 80 and over, Female, Male, Stroke, Time-to-Treatment

Citation

Published Version (Please cite this version)

10.1001/jama.2020.5697

Publication Info

Man, Shumei, Ying Xian, DaJuanicia N Holmes, Roland A Matsouaka, Jeffrey L Saver, Eric E Smith, Deepak L Bhatt, Lee H Schwamm, et al. (2020). Association Between Thrombolytic Door-to-Needle Time and 1-Year Mortality and Readmission in Patients With Acute Ischemic Stroke. JAMA, 323(21). pp. 2170–2184. 10.1001/jama.2020.5697 Retrieved from https://hdl.handle.net/10161/21835.

This is constructed from limited available data and may be imprecise. To cite this article, please review & use the official citation provided by the journal.

Scholars@Duke

Ying Xian

Adjunct Professor in the Department of Neurology

DaJuanicia Holmes

Assoc Dir, DCRI
Matsouaka

Roland Albert Matsouaka

Associate Professor of Biostatistics & Bioinformatics

Positions

  • Associate Professor of Biostatistics & Bioinformatics
  • Associate Chair for Culture, Engagement, and Impact 
  • Member of the Duke Clinical Research Institute

 

I am an Associate Professor in the Department of Biostatistics and Bioinformatics at Duke University and the Associate Chair for Culture, Engagement, and Impact in the Department of Biostatistics and Bioinformatics. I am also an Associate Director of Biostatistics and Data Science at the Duke Clinical Research Institute and member of the Consortium for the Holistic Assessment of Risk in Transplant (CHART).

 

The substantive areas of application of my research include biomedical,public health, and social sciences.   As a DCRI faculty statistician, I collaborate with clinical researchers to better understand and treat cardiovascular diseases. I have been actively involved in the analyses of large registry data, including the Society of Thoracic Surgeons (STS) National Database, the STS and American College of Cardiology (ACC) Transcatheter Valve Therapy (TVTR) Registry, and the American Heart Association/American Stroke Association Get With The Guidelines (GTWG).


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