Association of Pulmonary Hypertension With Clinical Outcomes of Transcatheter Mitral Valve Repair.


Journal

JAMA cardiology
ISSN: 2380-6591
Titre abrégé: JAMA Cardiol
Pays: United States
ID NLM: 101676033

Informations de publication

Date de publication:
01 01 2020
Historique:
pubmed: 21 11 2019
medline: 12 1 2021
entrez: 21 11 2019
Statut: ppublish

Résumé

Pulmonary hypertension (pHTN) is associated with increased risk of mortality after mitral valve surgery for mitral regurgitation. However, its association with clinical outcomes in patients undergoing transcatheter mitral valve repair (TMVr) with a commercially available system (MitraClip) is unknown. To assess the association of pHTN with readmissions for heart failure and 1-year all-cause mortality after TMVr. This retrospective cohort study analyzed 4071 patients who underwent TMVr with the MitraClip system from November 4, 2013, through March 31, 2017, across 232 US sites in the Society of Thoracic Surgery/American College of Cardiology Transcatheter Valve Therapy registry. Patients were stratified into the following 4 groups based on invasive mean pulmonary arterial pressure (mPAP): 1103 with no pHTN (mPAP, <25 mm Hg [group 1]); 1399 with mild pHTN (mPAP, 25-34 mm Hg [group 2]); 1011 with moderate pHTN (mPAP, 35-44 mm Hg [group 3]); and 558 with severe pHTN (mPAP, ≥45 mm Hg [group 4]). Data were analyzed from November 4, 2013, through March 31, 2017. Patients were stratified into groups before TMVr, and clinical outcomes were assessed at 1 year after intervention. Primary end point was a composite of 1-year mortality and readmissions for heart failure. Secondary end points were 30-day and 1-year mortality and readmissions for heart failure. Linkage to Centers for Medicare & Medicaid Services administrative claims was performed to assess 1-year outcomes in 2381 patients. Among the 4071 patients included in the analysis, the median age was 81 years (interquartile range, 73-86 years); 1885 (46.3%) were women and 2186 (53.7%) were men. The composite rate of 1-year mortality and readmissions for heart failure was 33.6% (95% CI, 31.6%-35.7%), which was higher in those with pHTN (27.8% [95% CI, 24.2%-31.5%] in group 1, 32.4% [95% CI, 29.0%-35.8%] in group 2, 36.0% [95% CI, 31.8%-40.2%] in group 3, and 45.2% [95% CI, 39.1%-51.0%] in group 4; P < .001). Similarly, 1-year mortality (16.3% [95% CI, 13.4%-19.5%] in group 1, 19.8% [95% CI, 17.0%-22.8%] in group 2, 22.4% [95% CI, 18.8%-26.1%] in group 3, and 27.8% [95% CI, 22.6%-33.3%] in group 4; P < .001) increased across pHTN groups. The association of pHTN with mortality persisted despite multivariable adjustment (hazard ratio per 5-mm Hg mPAP increase, 1.05; 95% CI, 1.01-1.09; P = .02). These findings suggest that pHTN is associated with increased mortality and readmission for heart failure in patients undergoing TMVr using the MitraClip system for severe mitral regurgitation. Further efforts are needed to determine whether earlier intervention before pHTN develops will improve clinical outcomes.

Identifiants

pubmed: 31746963
pii: 2755896
doi: 10.1001/jamacardio.2019.4428
pmc: PMC6902209
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

47-56

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Auteurs

Rasha Al-Bawardy (R)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

Sreekanth Vemulapalli (S)

Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina.

Vinod H Thourani (VH)

Marcus Valve Center, Department of Cardiac Surgery, Piedmont Heart and Vascular Institute, Atlanta, Georgia.

Michael Mack (M)

Department of Cardiology, Baylor Scott and White Heart Hospital Plano, Plano, Texas.

David Dai (D)

Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina.

Amanda Stebbins (A)

Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina.

Igor Palacios (I)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

Ignacio Inglessis (I)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

Rahul Sakhuja (R)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

Eyal Ben-Assa (E)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

Jonathan J Passeri (JJ)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

Jacob P Dal-Bianco (JP)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

Evin Yucel (E)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

Serguei Melnitchouk (S)

Cardiac Surgery Division, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston.

Gus J Vlahakes (GJ)

Cardiac Surgery Division, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston.

Arminder S Jassar (AS)

Cardiac Surgery Division, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston.

Sammy Elmariah (S)

Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.

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