Rheumatoid Arthritis Patients Have Better Outcomes Than Non-Rheumatoid Arthritis Patients When Hospitalized for Ischemic Stroke: Analysis of the National Inpatient Sample.


Journal

Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases
ISSN: 1536-7355
Titre abrégé: J Clin Rheumatol
Pays: United States
ID NLM: 9518034

Informations de publication

Date de publication:
01 Jan 2022
Historique:
pubmed: 15 9 2020
medline: 28 12 2021
entrez: 14 9 2020
Statut: ppublish

Résumé

The aims of this study were to compare the outcomes of patients primarily admitted for ischemic stroke with and without a secondary diagnosis of RA. Data were abstracted from the National Inpatient Sample (NIS) 2016 and 2017 database. The NIS was searched for hospitalizations for adult patients with ischemic stroke as principal diagnosis with and without RA as secondary diagnosis using International Classification of Diseases, 10th Revision codes. The primary outcome was inpatient mortality. Hospital length of stay (LOS), total hospital charges, odds of receiving tissue plasminogen activator, and mechanical thrombectomy were secondary outcomes of interest. Multivariate logistic and linear regression analyses were used accordingly to adjust for confounders. There were more than 71 million discharges included in the combined 2016 and 2017 NIS database. Of 525,570 patients with ischemic stroke, 8670 (1.7%) had RA. Hospitalizations for ischemic stroke with RA had less inpatient mortality (4.7% vs. 5.5%; adjusted odds ratio, 0.66; 95% confidence interval, 0.52-0.85; p = 0.001), shorter LOS (5.1 vs 5.7 days, p < 0.0001), lower mean total hospital charges ($61,626 vs. $70,345, p < 0.0001), and less odds of undergoing mechanical thrombectomy (3.9% vs. 5.1%; adjusted odds ratio, 0.55; 95% confidence interval, 0.42-0.72; p < 0.0001) compared with those without RA. Hospitalizations for ischemic stroke with RA had less inpatient mortality, shorter LOS, lower total hospital charges, and less likelihood of undergoing mechanical thrombectomy compared with those without RA. However, the odds of receiving tissue plasminogen activator were similar between both groups. Further studies to understand its mechanism would be helpful.

Identifiants

pubmed: 32925445
pii: 00124743-202201000-00013
doi: 10.1097/RHU.0000000000001563
doi:

Substances chimiques

Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13-e17

Informations de copyright

Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Ehizogie Edigin (E)

From the Department of Internal Medicine, John H Stroger Jr. Hospital of Cook County, Chicago IL.

Pius Ehiremen Ojemolon (PE)

Department of Anatomical Sciences, St. George's University, St. George's, Grenada.

Precious Obehi Eseaton (PO)

Department of Internal Medicine, University of Benin Teaching Hospital, Benin, Nigeria.

Hafeez Shaka (H)

From the Department of Internal Medicine, John H Stroger Jr. Hospital of Cook County, Chicago IL.

Emmanuel Akuna (E)

From the Department of Internal Medicine, John H Stroger Jr. Hospital of Cook County, Chicago IL.

Iriagbonse Rotimi Asemota (IR)

From the Department of Internal Medicine, John H Stroger Jr. Hospital of Cook County, Chicago IL.

Augustine Manadan (A)

Division of Rheumatology, Rush University Medical Center, Chicago IL.

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