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Transcatheter Aortic Valve Replacement Outcomes During the Public Health Emergency Flexibility Period.
Spoon, Daniel B; Tunis, Sean; Giri, Jay; Maddux, James T; Nathan, Ashwin; Chikermane, Soumya G; Reed, Michael; Schmoker, Joseph; Abicht, Travis; Walsh, Joseph; Heslop, Jeffrey; Zweifel, Jeff; Holmes, David.
Afiliação
  • Spoon DB; Providence Montana, Missoula, MT, USA. Electronic address: Daniel.Spoon@providence.org.
  • Tunis S; Rubix Health, Baltimore, MD, USA.
  • Giri J; University of Pennsylvania, Philadelphia, PA, USA.
  • Maddux JT; Providence Montana, Missoula, MT, USA.
  • Nathan A; University of Pennsylvania, Philadelphia, PA, USA.
  • Chikermane SG; Edwards Lifesciences, Irvine, CA, USA.
  • Reed M; Providence Montana, Missoula, MT, USA.
  • Schmoker J; Providence Montana, Missoula, MT, USA.
  • Abicht T; Providence Montana, Missoula, MT, USA.
  • Walsh J; St Alphonsus Health System, Boise, ID, USA.
  • Heslop J; St Alphonsus Health System, Boise, ID, USA.
  • Zweifel J; St Alphonsus Health System, Boise, ID, USA.
  • Holmes D; Mayo Clinic, Rochester, MN, USA.
Mayo Clin Proc ; 2024 Jul 05.
Article em En | MEDLINE | ID: mdl-39093263
ABSTRACT

OBJECTIVE:

To compare transcatheter aortic valve replacement (TAVR) outcomes during the period when public health emergency (PHE) flexibilities were in place with outcomes during a period before they were introduced.

METHODS:

Patients who received a native TAVR with either a SAPIEN 3 or SAPIEN 3 Ultra valve from the Society of Thoracic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry between June 22, 2019, and August 30, 2022, were placed into one of two cohorts (1) pre-PHE cohort, and (2) peri-PHE cohort. Outcomes included in-hospital events and events occurring 30 days post-TAVR. Patients were matched 11 on their propensity of receiving a TAVR during the pre- or peri-PHE periods. After matching, relative risk was calculated for each in-hospital outcome and HRs for outcomes 30 days post-TAVR.

RESULTS:

In this study, 173,434 patients met inclusion criteria; after 11 matching, there were 37,063 patients in each cohort. There was no difference between cohorts in in-hospital outcomes, including all-cause mortality, stroke, composite of mortality and stroke, pacemaker, or major vascular complications. Similarly, there was no statistically significant difference in 30-day outcomes between the cohorts.

CONCLUSION:

In this large-scale retrospective study of 74,126 patients undergoing TAVR procedures from 2019 to 2022, no significant differences existed in TAVR outcomes during the PHE period.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article