CT determined psoas muscle area predicts mortality in women undergoing transcatheter aortic valve implantation.


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 03 2019
Historique:
received: 18 05 2018
revised: 15 06 2018
accepted: 14 07 2018
pubmed: 13 9 2018
medline: 15 4 2020
entrez: 13 9 2018
Statut: ppublish

Résumé

The aim of this study was to assess the predictive value of PMA measurement for mortality. Current surgical risk stratification have limited predictive value in the transcatheter aortic valve implantation (TAVI) population. In TAVI workup, a CT scan is routinely performed but body composition is not analyzed. Psoas muscle area (PMA) reflects a patient's global muscle mass and accordingly PMA might serve as a quantifiable frailty measure. Multi-slice computed tomography scans (between 2010 and 2016) of 583 consecutive TAVI patients were reviewed. Patients were divided into equal sex-specific tertiles (low, mid, and high) according to an indexed PMA. Hazard ratios (HR) and their confidence intervals (CI) were determined for cardiac and all-cause mortality after TAVI. Low iPMA was associated with cardiac and all-cause mortality in females. One-year adjusted cardiac mortality HR in females for mid-iPMA and high-iPMA were 0.14 [95%CI, 0.05-0.45] and 0.40 [95%CI, 0.15-0.97], respectively. Similar effects were observed for 30-day and 2-years cardiac and all-cause mortality. In females, adding iPMA to surgical risk scores improved the predictive value for 1-year mortality. C-statistics changed from 0.63 [CI = 0.54-0.73] to 0.67 [CI: 0.58-0.75] for EuroSCORE II and from 0.67 [CI: 0.59-0.77] to 0.72 [CI: 0.63-0.80] for STS-PROM. Particularly in females, low iPMA is independently associated with an higher all-cause and cardiac mortality. Prospective studies should confirm whether PMA or other body composition parameters should be extracted automatically from CT-scans to include in clinical decision making and outcome prediction for TAVI.

Sections du résumé

OBJECTIVES
The aim of this study was to assess the predictive value of PMA measurement for mortality.
BACKGROUND
Current surgical risk stratification have limited predictive value in the transcatheter aortic valve implantation (TAVI) population. In TAVI workup, a CT scan is routinely performed but body composition is not analyzed. Psoas muscle area (PMA) reflects a patient's global muscle mass and accordingly PMA might serve as a quantifiable frailty measure.
METHODS
Multi-slice computed tomography scans (between 2010 and 2016) of 583 consecutive TAVI patients were reviewed. Patients were divided into equal sex-specific tertiles (low, mid, and high) according to an indexed PMA. Hazard ratios (HR) and their confidence intervals (CI) were determined for cardiac and all-cause mortality after TAVI.
RESULTS
Low iPMA was associated with cardiac and all-cause mortality in females. One-year adjusted cardiac mortality HR in females for mid-iPMA and high-iPMA were 0.14 [95%CI, 0.05-0.45] and 0.40 [95%CI, 0.15-0.97], respectively. Similar effects were observed for 30-day and 2-years cardiac and all-cause mortality. In females, adding iPMA to surgical risk scores improved the predictive value for 1-year mortality. C-statistics changed from 0.63 [CI = 0.54-0.73] to 0.67 [CI: 0.58-0.75] for EuroSCORE II and from 0.67 [CI: 0.59-0.77] to 0.72 [CI: 0.63-0.80] for STS-PROM.
CONCLUSIONS
Particularly in females, low iPMA is independently associated with an higher all-cause and cardiac mortality. Prospective studies should confirm whether PMA or other body composition parameters should be extracted automatically from CT-scans to include in clinical decision making and outcome prediction for TAVI.

Identifiants

pubmed: 30208263
doi: 10.1002/ccd.27823
pmc: PMC6585699
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

E248-E254

Informations de copyright

© 2018 The Authors. Catheterization and Cardiovascular Interventions published by Wiley Periodicals, Inc.

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Auteurs

Martijn S van Mourik (MS)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Yvonne C Janmaat (YC)

ACHIEVE - Centre of Applied Research, Amsterdam University of Applied Sciences, Amsterdam, The Netherlands.

Floortje van Kesteren (F)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.
Amsterdam UMC, University of Amsterdam, Department of Radiology, Amsterdam, The Netherlands.

Jeroen Vendrik (J)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

R Nils Planken (RN)

Amsterdam UMC, University of Amsterdam, Department of Radiology, Amsterdam, The Netherlands.

Marieke J Henstra (MJ)

Amsterdam UMC, University of Amsterdam, Department of Geriatrics, Amsterdam, The Netherlands.

Juliëtte F Velu (JF)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Wieneke Vlastra (W)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Aeilko H Zwinderman (AH)

Department of Clinical Epidemiology, Biostatistics and Bioinformatics, University of Amsterdam, Amsterdam, The Netherlands.

Karel T Koch (KT)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Robbert J de Winter (RJ)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Joanna J Wykrzykowska (JJ)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Jan J Piek (JJ)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

José P S Henriques (JPS)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Vincent R Lanting (VR)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Jan Baan (J)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

Corine Latour (C)

ACHIEVE - Centre of Applied Research, Amsterdam University of Applied Sciences, Amsterdam, The Netherlands.

Robert Lindeboom (R)

Department of Clinical Epidemiology, Biostatistics and Bioinformatics, University of Amsterdam, Amsterdam, The Netherlands.

M Marije Vis (MM)

Amsterdam UMC, University of Amsterdam, AMC Heartcenter, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.

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Classifications MeSH