The Association between Losartan Potassium Prescription and Postoperative Outcomes Following Total Knee Arthroplasty: A TriNetX Analysis.

Losartan Total Knee Arthroplasty TriNetX angiotensin receptor blocker arthrofibrosis manipulation under anesthesia

Journal

Orthopaedics & traumatology, surgery & research : OTSR
ISSN: 1877-0568
Titre abrégé: Orthop Traumatol Surg Res
Pays: France
ID NLM: 101494830

Informations de publication

Date de publication:
28 Feb 2024
Historique:
received: 27 09 2023
revised: 19 02 2024
accepted: 22 02 2024
medline: 2 3 2024
pubmed: 2 3 2024
entrez: 1 3 2024
Statut: aheadofprint

Résumé

Total knee arthroplasty (TKA) is a common surgical procedure performed to alleviate pain and improve functional outcomes in patients with knee osteoarthritis and rheumatoid arthritis who have failed conservative treatments. Arthrofibrosis has been extensively studied due to its negative impact on TKA outcomes. Losartan, an angiotensin receptor blocker (ARB), has the potential to improve TKA outcomes by inhibiting TGF-β and decreasing fibrosis. This study aims to analyze a large-scale, real-world healthcare database to investigate the association between losartan potassium prescription and postoperative outcomes such as readmissions, ED visits, and the need for MUA or revision TKA. Based on previous literature and the nature of ARBs, it is expected that the addition of losartan will aid in better outcomes for patients following a primary TKA. In this retrospective observational study, the TriNetX Research Network (TriNetX) database was queried as of June 21, 2023. All patients who underwent a primary total knee arthroplasty (TKA) prior to June 21, 2022 were included. Patients were then divided into two cohorts by whether they had an active losartan potassium prescription within the year prior to their surgery to within 90 days postoperatively. Patients were then propensity-matched to eliminate differences in demographics and comorbidities. Losartan TKA patients were 1.18 (OR: 0.85 (95% CI: 0.79, 0.90), p < 0.001) times less likely to be readmitted within 90 days and were 1.15 (OR: 0.87 (95% CI: 0.79, 0.96); p = 0.009) times less likely to undergo a manipulation under anesthesia (MUA) within the 1-year postoperative period. There were no statistically significant differences in rates of Emergency Department (ED) visits at 90 days postoperatively or revision TKAs at 1 year postoperatively. In conclusion, patients with an active losartan prescription prior to TKA had a significantly lower likelihood of readmission within 90 days and a lower likelihood of undergoing MUA within the 1-year postoperative period compared to patients not taking losartan. This presents an opportunity for further clinical investigation to explore the value of losartan in TKA. III; an observational cohort study.

Sections du résumé

BACKGROUND BACKGROUND
Total knee arthroplasty (TKA) is a common surgical procedure performed to alleviate pain and improve functional outcomes in patients with knee osteoarthritis and rheumatoid arthritis who have failed conservative treatments. Arthrofibrosis has been extensively studied due to its negative impact on TKA outcomes. Losartan, an angiotensin receptor blocker (ARB), has the potential to improve TKA outcomes by inhibiting TGF-β and decreasing fibrosis. This study aims to analyze a large-scale, real-world healthcare database to investigate the association between losartan potassium prescription and postoperative outcomes such as readmissions, ED visits, and the need for MUA or revision TKA.
HYPOTHESIS OBJECTIVE
Based on previous literature and the nature of ARBs, it is expected that the addition of losartan will aid in better outcomes for patients following a primary TKA.
PATIENTS AND METHODS METHODS
In this retrospective observational study, the TriNetX Research Network (TriNetX) database was queried as of June 21, 2023. All patients who underwent a primary total knee arthroplasty (TKA) prior to June 21, 2022 were included. Patients were then divided into two cohorts by whether they had an active losartan potassium prescription within the year prior to their surgery to within 90 days postoperatively. Patients were then propensity-matched to eliminate differences in demographics and comorbidities.
RESULTS RESULTS
Losartan TKA patients were 1.18 (OR: 0.85 (95% CI: 0.79, 0.90), p < 0.001) times less likely to be readmitted within 90 days and were 1.15 (OR: 0.87 (95% CI: 0.79, 0.96); p = 0.009) times less likely to undergo a manipulation under anesthesia (MUA) within the 1-year postoperative period. There were no statistically significant differences in rates of Emergency Department (ED) visits at 90 days postoperatively or revision TKAs at 1 year postoperatively.
DISCUSSION CONCLUSIONS
In conclusion, patients with an active losartan prescription prior to TKA had a significantly lower likelihood of readmission within 90 days and a lower likelihood of undergoing MUA within the 1-year postoperative period compared to patients not taking losartan. This presents an opportunity for further clinical investigation to explore the value of losartan in TKA.
LEVEL OF EVIDENCE METHODS
III; an observational cohort study.

Identifiants

pubmed: 38428487
pii: S1877-0568(24)00059-8
doi: 10.1016/j.otsr.2024.103851
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103851

Informations de copyright

Copyright © 2024. Published by Elsevier Masson SAS.

Auteurs

Parimal Rana (P)

Luminis Health Orthopedics, Anne Arundel Medical Center, Annapolis, MD, United States.

Jane Brennan (J)

Luminis Health Orthopedics, Anne Arundel Medical Center, Annapolis, MD, United States.

Andrea Johnson (A)

Luminis Health Orthopedics, Anne Arundel Medical Center, Annapolis, MD, United States.

Justin Turcotte (J)

Luminis Health Orthopedics, Anne Arundel Medical Center, Annapolis, MD, United States. Electronic address: jturcotte@aahs.org.

James H MacDonald (JH)

Luminis Health Orthopedics, Anne Arundel Medical Center, Annapolis, MD, United States.

Paul King (P)

Luminis Health Orthopedics, Anne Arundel Medical Center, Annapolis, MD, United States.

Classifications MeSH