Association of peripheral artery disease with in-hospital outcomes after endovascular transcatheter aortic valve replacement.


Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
01 Aug 2019
Historique:
received: 05 04 2019
accepted: 10 04 2019
pubmed: 27 4 2019
medline: 4 8 2020
entrez: 27 4 2019
Statut: ppublish

Résumé

The aim of this study was to determine the prevalence of peripheral artery disease (PAD) and its association with in-hospital outcomes after endovascular transcatheter aortic valve replacement (EV-TAVR). TAVR is an established treatment for patients at prohibitive, high, or intermediate surgical risk. PAD is a significant comorbidity in the determination of surgical risk. However, data on association of PAD with outcomes after EV-TAVR are limited. Patients in the National Inpatient Sample who underwent EV-TAVR between January 1, 2012 and September 30, 2015 were evaluated. The primary outcome was in-hospital mortality. A total of 51,685 patients underwent EV-TAVR during the study period. Of these, 12,740 (24.6%) had a coexisting diagnosis of PAD. The adjusted odds for in-hospital mortality [OR 1.08 (95% CI 0.83-1.41)], permanent pacemaker implantation [OR 0.98 (0.85-1.14)], conversion to open aortic valve replacement [OR 1.05 (0.49-2.26)], or acute myocardial infarction [OR 1.31(0.99-1.71)] were not different in patients with versus without PAD. However, patients with PAD had greater adjusted odds of vascular complications [OR 1.80 (1.50-2.16)], major bleeding [OR 1.20 (1.09-1.34)], acute kidney injury (AKI) [OR 1.19 (1.05-1.36)], cardiac complications [aOR 1.21 (1.01-1.44)], and stroke [OR 1.39(1.10-1.75)] compared with patients without PAD. Length of stay (LOS) was significantly longer for patients with PAD [7.23 (0.14) days vs. 7.11 (0.1) days, p < 0.001]. Of patients undergoing EV-TAVR, ~25% have coexisting PAD. PAD was not associated with increased risk of in-hospital mortality but was associated with higher risk of vascular complications, major bleeding, AKI, stroke, cardiac complications, and longer LOS.

Sections du résumé

OBJECTIVES OBJECTIVE
The aim of this study was to determine the prevalence of peripheral artery disease (PAD) and its association with in-hospital outcomes after endovascular transcatheter aortic valve replacement (EV-TAVR).
BACKGROUND BACKGROUND
TAVR is an established treatment for patients at prohibitive, high, or intermediate surgical risk. PAD is a significant comorbidity in the determination of surgical risk. However, data on association of PAD with outcomes after EV-TAVR are limited.
METHODS METHODS
Patients in the National Inpatient Sample who underwent EV-TAVR between January 1, 2012 and September 30, 2015 were evaluated. The primary outcome was in-hospital mortality.
RESULTS RESULTS
A total of 51,685 patients underwent EV-TAVR during the study period. Of these, 12,740 (24.6%) had a coexisting diagnosis of PAD. The adjusted odds for in-hospital mortality [OR 1.08 (95% CI 0.83-1.41)], permanent pacemaker implantation [OR 0.98 (0.85-1.14)], conversion to open aortic valve replacement [OR 1.05 (0.49-2.26)], or acute myocardial infarction [OR 1.31(0.99-1.71)] were not different in patients with versus without PAD. However, patients with PAD had greater adjusted odds of vascular complications [OR 1.80 (1.50-2.16)], major bleeding [OR 1.20 (1.09-1.34)], acute kidney injury (AKI) [OR 1.19 (1.05-1.36)], cardiac complications [aOR 1.21 (1.01-1.44)], and stroke [OR 1.39(1.10-1.75)] compared with patients without PAD. Length of stay (LOS) was significantly longer for patients with PAD [7.23 (0.14) days vs. 7.11 (0.1) days, p < 0.001].
CONCLUSION CONCLUSIONS
Of patients undergoing EV-TAVR, ~25% have coexisting PAD. PAD was not associated with increased risk of in-hospital mortality but was associated with higher risk of vascular complications, major bleeding, AKI, stroke, cardiac complications, and longer LOS.

Identifiants

pubmed: 31025488
doi: 10.1002/ccd.28310
pmc: PMC6832693
mid: NIHMS1056823
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

249-255

Subventions

Organisme : CSRD VA
ID : IK2 CX001074
Pays : United States
Organisme : Biomedical Laboratory Research & Development Service

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

Circ Cardiovasc Interv. 2018 Apr;11(4):e006179
pubmed: 29643130
N Engl J Med. 2010 Oct 21;363(17):1597-607
pubmed: 20961243
J Am Coll Cardiol. 2015 May 26;65(20):2184-94
pubmed: 25787196
JACC Cardiovasc Interv. 2017 Jul 24;10(14):1436-1446
pubmed: 28728657
J Am Soc Nephrol. 2000 Apr;11(4):778-83
pubmed: 10752538
Circ Cardiovasc Interv. 2017 Oct;10(10):null
pubmed: 28951396
J Am Coll Cardiol. 2016 Apr 26;67(16):1901-13
pubmed: 27012780
Eur Heart J. 2015 Jun 21;36(24):1494-5
pubmed: 26295080
Mayo Clin Proc. 2004 Sep;79(9):1107-9
pubmed: 15357030
J Vasc Surg. 2014 Sep;60(3):686-95.e2
pubmed: 24820900
Circ Cardiovasc Interv. 2017 Oct;10(10):
pubmed: 29042398
Vasc Med. 2017 Jun;22(3):234-244
pubmed: 28494713
Am J Cardiol. 2015 Jan 1;115(1):100-6
pubmed: 25456874
JACC Cardiovasc Interv. 2011 Aug;4(8):851-8
pubmed: 21851897
EuroIntervention. 2010 Jan;5(6):666-72
pubmed: 20142216
Catheter Cardiovasc Interv. 2018 Feb 1;91(2):330-342
pubmed: 28738447
N Engl J Med. 2011 Jun 9;364(23):2187-98
pubmed: 21639811

Auteurs

Divyanshu Mohananey (D)

Division of Cardiovascular Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

Pedro Villablanca (P)

Center for Structural Heart Disease, Henry Ford Health System, Detroit, Michigan.

Tanush Gupta (T)

Division of Cardiology, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York.

Sagar Ranka (S)

Department of Medicine, John H. Stroger, Jr. Hospital of Cook County, Chicago, Illinois.

Nirmanmoh Bhatia (N)

Division of Cardiovascular Medicine, Vanderbilt, University Medical Center, Nashville, Tennessee.

Oluwole Adegbala (O)

Department of Internal Medicine, Englewood Hospital and Medical Center, Seton Hall University-Hackensack Meridian School of Medicine, South Orange, New Jersey.

Tomo Ando (T)

Division of Cardiology, Wayne State University/Detroit Medical Center, Detroit, Michigan.

Dee Dee Wang (DD)

Center for Structural Heart Disease, Henry Ford Health System, Detroit, Michigan.

Jose M Wiley (JM)

Division of Cardiology, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York.

Marvin Eng (M)

Center for Structural Heart Disease, Henry Ford Health System, Detroit, Michigan.

Ankur Kalra (A)

Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.

Harish Ramakrishna (H)

Department of Anesthesiology, Mayo Clinic, Scottsdale, Arizona.

Binita Shah (B)

Leon H. Charney Division of Cardiology, New York University, New York, New York.

William O'Neill (W)

Center for Structural Heart Disease, Henry Ford Health System, Detroit, Michigan.

Jorge Saucedo (J)

Division of Cardiovascular Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

Deepak L Bhatt (DL)

Brigham and Women's Hospital Heart & Vascular Center, Harvard Medical School, Boston, Massachusetts.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH