Natural History of Functional Tricuspid Regurgitation Quantified by Cardiovascular Magnetic Resonance.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
15 09 2020
Historique:
received: 11 06 2020
revised: 10 07 2020
accepted: 13 07 2020
entrez: 11 9 2020
pubmed: 12 9 2020
medline: 27 1 2021
Statut: ppublish

Résumé

Quantitation of tricuspid regurgitant (TR) severity can be challenging with conventional echocardiographic imaging and may be better evaluated using cardiovascular magnetic resonance (CMR). In patients with functional TR, this study sought to examine the relationship between TR volume (TRVol) and TR fraction (TRF) with all-cause mortality. We examined 547 patients with functional TR using CMR to quantify TRVol and TRF. The primary outcome was all-cause mortality. Thresholds for mild, moderate, and severe TR were derived based on natural history outcome data. During a median follow-up of 2.6 years (interquartile range: 1.7 to 3.3 years), there were 93 deaths, with an estimated 5-year survival of 79% (95% confidence interval [CI]: 73% to 83%). After adjustment of clinical and imaging variables, including RV function, both TRF (adjusted hazard ratio [AHR] per 10% increment: 1.26; 95% CI: 1.10 to 1.45; p = 0.001) and TRVol (AHR per 10-ml increment: 1.15; 95% CI: 1.04 to 1.26; p = 0.004) were associated with mortality. Patients in the highest-risk strata of TRVol ≥45 ml or TRF ≥50% had the worst prognosis (AHR: 2.26; 95% CI: 1.36 to 3.76; p = 0.002 for TRVol and AHR: 2.60; 95% CI: 1.45 to 4.66; p = 0.001 for TRF). This is the first study to use CMR to assess independent prognostic implications of functional TR. Both TRF and TRVol were associated with increased mortality after adjustment for clinical and imaging covariates, including right ventricular ejection fraction. A TRVol of ≥45 ml or TRF of ≥50% identified patients in the highest-risk strata for mortality. These CMR thresholds should be used for patient selection in future trials to determine if tricuspid valve intervention improves outcomes in this high-risk group.

Sections du résumé

BACKGROUND
Quantitation of tricuspid regurgitant (TR) severity can be challenging with conventional echocardiographic imaging and may be better evaluated using cardiovascular magnetic resonance (CMR).
OBJECTIVES
In patients with functional TR, this study sought to examine the relationship between TR volume (TRVol) and TR fraction (TRF) with all-cause mortality.
METHODS
We examined 547 patients with functional TR using CMR to quantify TRVol and TRF. The primary outcome was all-cause mortality. Thresholds for mild, moderate, and severe TR were derived based on natural history outcome data.
RESULTS
During a median follow-up of 2.6 years (interquartile range: 1.7 to 3.3 years), there were 93 deaths, with an estimated 5-year survival of 79% (95% confidence interval [CI]: 73% to 83%). After adjustment of clinical and imaging variables, including RV function, both TRF (adjusted hazard ratio [AHR] per 10% increment: 1.26; 95% CI: 1.10 to 1.45; p = 0.001) and TRVol (AHR per 10-ml increment: 1.15; 95% CI: 1.04 to 1.26; p = 0.004) were associated with mortality. Patients in the highest-risk strata of TRVol ≥45 ml or TRF ≥50% had the worst prognosis (AHR: 2.26; 95% CI: 1.36 to 3.76; p = 0.002 for TRVol and AHR: 2.60; 95% CI: 1.45 to 4.66; p = 0.001 for TRF).
CONCLUSIONS
This is the first study to use CMR to assess independent prognostic implications of functional TR. Both TRF and TRVol were associated with increased mortality after adjustment for clinical and imaging covariates, including right ventricular ejection fraction. A TRVol of ≥45 ml or TRF of ≥50% identified patients in the highest-risk strata for mortality. These CMR thresholds should be used for patient selection in future trials to determine if tricuspid valve intervention improves outcomes in this high-risk group.

Identifiants

pubmed: 32912443
pii: S0735-1097(20)36035-6
doi: 10.1016/j.jacc.2020.07.036
pii:
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1291-1301

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Yang Zhan (Y)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas; Department of Cardiology, Regina General Hospital, University of Saskatchewan, Regina, Saskatchewan, Canada.

Dany Debs (D)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

Mohammad A Khan (MA)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

Duc T Nguyen (DT)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

Edward A Graviss (EA)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Department of Surgery, Houston Methodist Hospital, Houston, Texas.

Shaden Khalaf (S)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

Stephen H Little (SH)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

Michael J Reardon (MJ)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

Sherif Nagueh (S)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

Miguel A Quiñones (MA)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

Neal Kleiman (N)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

William A Zoghbi (WA)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas.

Dipan J Shah (DJ)

Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas. Electronic address: djshah@houstonmethodist.org.

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