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“Weekend Effect” on 30-Day Readmissions among Stroke Survivors: An Analysis of the National Readmission Database

BACKGROUND AND PURPOSE: Previous studies suggested that quality of care may be lower on weekends than during the week. We hypothesized that, among patients hospitalized for an index ischemic stroke, those admitted on weekends would have a higher risk of 30-day readmission than those admitted on week...

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Autores principales: Khaksari, Bijan J., Kulick, Erin R., Elkind, Mitchell S.V., Boehme, Amelia K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036528/
https://www.ncbi.nlm.nih.gov/pubmed/31234190
http://dx.doi.org/10.1159/000500611
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author Khaksari, Bijan J.
Kulick, Erin R.
Elkind, Mitchell S.V.
Boehme, Amelia K.
author_facet Khaksari, Bijan J.
Kulick, Erin R.
Elkind, Mitchell S.V.
Boehme, Amelia K.
author_sort Khaksari, Bijan J.
collection PubMed
description BACKGROUND AND PURPOSE: Previous studies suggested that quality of care may be lower on weekends than during the week. We hypothesized that, among patients hospitalized for an index ischemic stroke, those admitted on weekends would have a higher risk of 30-day readmission than those admitted on weekdays. METHODS: We utilized the 2013 Nationwide Readmission Database, which includes data on US inpatient admissions from the Agency for Healthcare Research and Quality Healthcare Utilization Project. The database includes a nationally representative weighted probability sample of inpatient hospitalizations regardless of insurance status. Patients with primary acute ischemic stroke were identified using previously validated ICD-9-CM diagnosis codes. We conducted a weighted analysis using survey design logistic regression models to estimate crude and adjusted odds ratios (OR) and 95% confidence intervals (95% CI) for the association between weekend admission and 30-day readmission in ischemic stroke patients. RESULTS: Among 319,317 patients admitted for ischemic stroke, 12.1% were readmitted within 30 days. Those with 30-day readmissions had an average of 8 chronic conditions, and all cardiovascular-related comorbidities increased the risk of 30-day readmissions. Ischemic stroke patients admitted on weekends had odds of 30-day readmission similar to patients admitted on weekdays (OR 1.02; 95% CI 0.98–1.06). Weekend admission also did not affect readmission at 7 or 60 days. CONCLUSIONS: We found no association between weekend admission and 30-day readmissions, providing indirect evidence of homogeneity in the quality of care delivered during week day and weekend admissions.
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spelling pubmed-70365282020-02-26 “Weekend Effect” on 30-Day Readmissions among Stroke Survivors: An Analysis of the National Readmission Database Khaksari, Bijan J. Kulick, Erin R. Elkind, Mitchell S.V. Boehme, Amelia K. Cerebrovasc Dis Extra Original Paper BACKGROUND AND PURPOSE: Previous studies suggested that quality of care may be lower on weekends than during the week. We hypothesized that, among patients hospitalized for an index ischemic stroke, those admitted on weekends would have a higher risk of 30-day readmission than those admitted on weekdays. METHODS: We utilized the 2013 Nationwide Readmission Database, which includes data on US inpatient admissions from the Agency for Healthcare Research and Quality Healthcare Utilization Project. The database includes a nationally representative weighted probability sample of inpatient hospitalizations regardless of insurance status. Patients with primary acute ischemic stroke were identified using previously validated ICD-9-CM diagnosis codes. We conducted a weighted analysis using survey design logistic regression models to estimate crude and adjusted odds ratios (OR) and 95% confidence intervals (95% CI) for the association between weekend admission and 30-day readmission in ischemic stroke patients. RESULTS: Among 319,317 patients admitted for ischemic stroke, 12.1% were readmitted within 30 days. Those with 30-day readmissions had an average of 8 chronic conditions, and all cardiovascular-related comorbidities increased the risk of 30-day readmissions. Ischemic stroke patients admitted on weekends had odds of 30-day readmission similar to patients admitted on weekdays (OR 1.02; 95% CI 0.98–1.06). Weekend admission also did not affect readmission at 7 or 60 days. CONCLUSIONS: We found no association between weekend admission and 30-day readmissions, providing indirect evidence of homogeneity in the quality of care delivered during week day and weekend admissions. S. Karger AG 2019-06-24 /pmc/articles/PMC7036528/ /pubmed/31234190 http://dx.doi.org/10.1159/000500611 Text en Copyright © 2019 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Original Paper
Khaksari, Bijan J.
Kulick, Erin R.
Elkind, Mitchell S.V.
Boehme, Amelia K.
“Weekend Effect” on 30-Day Readmissions among Stroke Survivors: An Analysis of the National Readmission Database
title “Weekend Effect” on 30-Day Readmissions among Stroke Survivors: An Analysis of the National Readmission Database
title_full “Weekend Effect” on 30-Day Readmissions among Stroke Survivors: An Analysis of the National Readmission Database
title_fullStr “Weekend Effect” on 30-Day Readmissions among Stroke Survivors: An Analysis of the National Readmission Database
title_full_unstemmed “Weekend Effect” on 30-Day Readmissions among Stroke Survivors: An Analysis of the National Readmission Database
title_short “Weekend Effect” on 30-Day Readmissions among Stroke Survivors: An Analysis of the National Readmission Database
title_sort “weekend effect” on 30-day readmissions among stroke survivors: an analysis of the national readmission database
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036528/
https://www.ncbi.nlm.nih.gov/pubmed/31234190
http://dx.doi.org/10.1159/000500611
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