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Effect on 30-Day Readmissions after Early Versus Delayed Discharge after Uncomplicated Transcatheter Aortic Valve Implantation (from the Nationwide Readmissions Database)

  • Mohamed A. Omer
  • , Kim Smolderen
  • , Kevin Kennedy
  • , Islam Y. Elgendy
  • , Dhaval Kolte
  • , Philip G. Jones
  • , John A. Spertus
  • , Suzanne V. Arnold

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Early discharge after transcatheter aortic valve implantation has been shown to be safe in single-center studies and trials, but outcomes in broader clinical practice are unknown. Using the National Readmission Databases (1/2014 to 9/2015), we compared 30-day readmission rates between early (<3 days) and late (≥3 days) discharges after uncomplicated endovascular TAVR in a propensity-matched cohort. We examined factors associated with failure of early discharge by testing for interactions of patient factors with discharge strategy. Among 4,955 hospitalizations for uncomplicated TAVR, 1,857 (37%) were discharged early with substantial site-level variability (range 0% to 87%; median odds ratio 3.69). In the propensity matched cohort (n = 3,346), there were similar rates of 30-day readmission by discharge strategy (early vs late: 10.3% vs 10.6%; stratified log-rank p = 0.555). There was a statistically significant interaction between discharge strategy and number of chronic conditions (p = 0.007), where readmission rates were lower in patients discharged early in those with 0 to 4 chronic conditions, but not in those with 5 to 10 or >10. In conclusion, in a large “real-world” cohort, early discharge after uncomplicated TAVR was not associated with a higher rate of 30-day rehospitalization, yet there was significant variability across US hospitals. No patient characteristics were associated with increased risk of readmission with early discharge.

Original languageEnglish
Pages (from-to)100-106
Number of pages7
JournalAmerican Journal of Cardiology
Volume125
Issue number1
DOIs
StatePublished - Jan 1 2020

Bibliographical note

Publisher Copyright:
© 2019 Elsevier Inc.

Funding

Dr. Smolderen is supported by an unrestricted research grant by Merck and Boston Scientific (PCORI, Grant/Award Number: CE-1304-6677; Boston Scientific; Merck). Dr. Spertus reports research grants from Lilly, Novartis and Abbott Vascular. He has served as a consultant for Novartis, Amgen, Bayer and United Healthcare. He owns the copyright to the SAQ, and has an equity interest in Health Outcomes Sciences. The remaining authors have no disclosures to report. Dr. Smolderen is supported by an unrestricted research grant by Merck and Boston Scientific (PCORI, Grant/Award Number: CE-1304-6677 ; Boston Scientific; Merck). Dr. Spertus reports research grants from Lilly, Novartis and Abbott Vascular. He has served as a consultant for Novartis, Amgen, Bayer and United Healthcare. He owns the copyright to the SAQ, and has an equity interest in Health Outcomes Sciences. The remaining authors have no disclosures to report.

FundersFunder number
Merck and Boston Scientific
United Healthcare
AMGen
Eli Lilly and Company
Merck
Novartis
Patient-Centered Outcomes Research InstituteCE-1304-6677
Bayer Corporation
Abbott Vascular

    ASJC Scopus subject areas

    • Cardiology and Cardiovascular Medicine

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