Achieving More Rapid Door-to-Needle Times and Improved Outcomes in Acute Ischemic Stroke in a Nationwide Quality Improvement Intervention

Author:

Xian Ying1,Xu Haolin2,Smith Eric E.3,Saver Jeffrey L.4,Reeves Mathew J.5,Bhatt Deepak L.6,Hernandez Adrian F.2ORCID,Peterson Eric D.7,Schwamm Lee H.8,Fonarow Gregg C.9ORCID

Affiliation:

1. Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX. (Y.X.)

2. Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (H.X., A.F.H.).

3. Department of Clinical Neurosciences, Hotchkiss Brian Institute, University of Calgary, Canada (E.E.S.).

4. Department of Neurology, University of California, Los Angeles (J.L.S.).

5. Department of Epidemiology, Michigan State University, East Lansing (M.J.R.).

6. Brigham and Women’s Hospital Heart and Vascular Center and Harvard Medical School, Boston, MA (D.L.B.).

7. Division of Cardiology, University of Texas Southwestern Medical Center, Dallas, TX. (E.D.P.)

8. Department of Neurology, Massachusetts General Hospital, Boston (L.H.S.).

9. Division of Cardiology, University of California at Los Angeles (G.C.F.).

Abstract

Background and Purpose: The benefits of tPA (tissue-type plasminogen activator) in acute ischemic stroke are time-dependent. However, delivery of thrombolytic therapy rapidly after hospital arrival was initially occurring infrequently in hospitals in the United States, discrepant with national guidelines. Methods: We evaluated door-to-needle (DTN) times and clinical outcomes among patients with acute ischemic stroke receiving tPA before and after initiation of 2 successive nationwide quality improvement initiatives: Target: Stroke Phase I (2010–2013) and Target: Stroke Phase II (2014–2018) from 913 Get With The Guidelines-Stroke hospitals in the United States between April 2003 and September 2018. Results: Among 154 221 patients receiving tPA within 3 hours of stroke symptom onset (median age 72 years, 50.1% female), median DTN times decreased from 78 minutes (interquartile range, 60–98) preintervention, to 66 minutes (51–87) during Phase I, and 50 minutes (37–66) during Phase II ( P <0.001). Proportions of patients with DTN ≤60 minutes increased from 26.4% to 42.7% to 68.6% ( P <0.001). Proportions of patients with DTN ≤45 minutes increased from 10.1% to 17.7% to 41.4% ( P <0.001). By the end of the second intervention, 75.4% and 51.7% patients achieved 60-minute and 45-minute DTN goals. Compared with the preintervention period, hospitals during the second intervention period (2014–2018) achieved higher rates of tPA use (11.7% versus 5.6%; adjusted odds ratio, 2.43 [95% CI, 2.31–2.56]), lower in-hospital mortality (6.0% versus 10.0%; adjusted odds ratio, 0.69 [0.64–0.73]), fewer bleeding complication (3.4% versus 5.5%; adjusted odds ratio, 0.68 [0.62–0.74]), and higher rates of discharge to home (49.6% versus 35.7%; adjusted odds ratio, 1.43 [1.38–1.50]). Similar findings were found in sensitivity analyses of 185 501 patients receiving tPA within 4.5 hours of symptom onset. Conclusions: A nationwide quality improvement program for acute ischemic stroke was associated with substantial improvement in the timeliness of thrombolytic therapy start, increased thrombolytic treatment, and improved clinical outcomes.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

Reference35 articles.

1. Target: Stroke Phase I 17 743/39 456 (45.0) 1.05 (0.99-1.12)

2. Target: Stroke Phase II 49 629/92 782 (53.5) 1.36 (1.28-1.45)

3. Tissue plasminogen activator for acute ischemic stroke;The National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group;N Engl J Med.,1995

4. Thrombolysis with alteplase 3 to 4.5 hours after acute ischemic stroke;Hacke W;N Engl J Med.,2008

5. Association of outcome with early stroke treatment: pooled analysis of ATLANTIS, ECASS, and NINDS rt-PA stroke trials;Hacke W;Lancet.,2004

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