Pulmonary Artery Proportional Pulse Pressure (PAPP) Index Identifies Patients With Improved Survival From the CardioMEMS Implantable Pulmonary Artery Pressure Monitor.


Journal

Heart, lung & circulation
ISSN: 1444-2892
Titre abrégé: Heart Lung Circ
Pays: Australia
ID NLM: 100963739

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 17 07 2020
revised: 29 12 2020
accepted: 07 03 2021
pubmed: 18 4 2021
medline: 30 9 2021
entrez: 17 4 2021
Statut: ppublish

Résumé

Pulmonary artery proportional pulse pressure (PAPP) was recently shown to have prognostic value in heart failure (HF) with reduced ejection fraction (HFrEF) and pulmonary hypertension. We tested the hypothesis that PAPP would be predictive of adverse outcomes in patients with implantable pulmonary artery pressure monitor (CardioMEMS™ HF System, St. Jude Medical [now Abbott], Atlanta, GA, USA). Survival analysis with Cox proportional hazards regression was used to evaluate all-cause deaths and HF hospitalisation (HFH) in CHAMPION trial Among 550 randomised patients, 274 had PAPP ≤ the median value of 0.583 while 276 had PAPP>0.583. Patients with PAPP≤0.583 (versus PAPP>0.583) had an increased risk of HFH (HR 1.40, 95% CI 1.16-1.68, p=0.0004) and experienced a significant 46% reduction in annualised risk of death with CardioMEMS treatment (HR 0.54, 95% CI 0.31-0.92) during 2-3 years of follow-up. This survival benefit was attributable to the treatment benefit in patients with HFrEF and PAPP≤0.583 (HR 0.50, 95% CI 0.28-0.90, p<0.05). Patients with PAPP>0.583 or HF with preserved EF (HFpEF) had no significant survival benefit with treatment (p>0.05). Lower PAPP in HFrEF patients with CardioMEMS constitutes a higher mortality risk status. More studies are needed to understand clinical applications of PAPP in implantable pulmonary artery pressure monitors.

Sections du résumé

BACKGROUND BACKGROUND
Pulmonary artery proportional pulse pressure (PAPP) was recently shown to have prognostic value in heart failure (HF) with reduced ejection fraction (HFrEF) and pulmonary hypertension. We tested the hypothesis that PAPP would be predictive of adverse outcomes in patients with implantable pulmonary artery pressure monitor (CardioMEMS™ HF System, St. Jude Medical [now Abbott], Atlanta, GA, USA).
METHODS METHODS
Survival analysis with Cox proportional hazards regression was used to evaluate all-cause deaths and HF hospitalisation (HFH) in CHAMPION trial
RESULTS RESULTS
Among 550 randomised patients, 274 had PAPP ≤ the median value of 0.583 while 276 had PAPP>0.583. Patients with PAPP≤0.583 (versus PAPP>0.583) had an increased risk of HFH (HR 1.40, 95% CI 1.16-1.68, p=0.0004) and experienced a significant 46% reduction in annualised risk of death with CardioMEMS treatment (HR 0.54, 95% CI 0.31-0.92) during 2-3 years of follow-up. This survival benefit was attributable to the treatment benefit in patients with HFrEF and PAPP≤0.583 (HR 0.50, 95% CI 0.28-0.90, p<0.05). Patients with PAPP>0.583 or HF with preserved EF (HFpEF) had no significant survival benefit with treatment (p>0.05).
CONCLUSION CONCLUSIONS
Lower PAPP in HFrEF patients with CardioMEMS constitutes a higher mortality risk status. More studies are needed to understand clinical applications of PAPP in implantable pulmonary artery pressure monitors.

Identifiants

pubmed: 33863665
pii: S1443-9506(21)00105-0
doi: 10.1016/j.hlc.2021.03.004
pii:
doi:

Substances chimiques

Piperazines 0
LY 165163 8HAJ699EWG

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1389-1396

Informations de copyright

Copyright © 2021 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved.

Auteurs

Sula Mazimba (S)

University of Virginia Health System, Charlottesville, VA, USA. Electronic address: SM8SD@hscmail.mcc.virginia.edu.

Greg Ginn (G)

Global Research and Development, St. Jude Medical, Sylmar, CA, USA.

Hunter Mwansa (H)

Case Western Reserve University/St Vincent Charity Medical Center, Cleveland, OH, USA.

Olusola Laja (O)

University of Virginia Health System, Charlottesville, VA, USA.

Christiana Jeukeng (C)

University of Virginia Health System, Charlottesville, VA, USA.

Comfort Elumogo (C)

University of Virginia Health System, Charlottesville, VA, USA.

Brandy Patterson (B)

University of Virginia Health System, Charlottesville, VA, USA.

Jamie L W Kennedy (JLW)

University of Virginia Health System, Charlottesville, VA, USA.

Nishaki Mehta (N)

University of Virginia Health System, Charlottesville, VA, USA.

John A Hossack (JA)

Department of Biomedical, Electrical and Computer Engineering, University of Virginia Health System, Charlottesville, VA, USA.

Alex M Parker (AM)

University of Virginia Health System, Charlottesville, VA, USA.

Andrew Mihalek (A)

University of Virginia Health System, Charlottesville, VA, USA.

Jose Tallaj (J)

University of Alabama at Birmingham, Birmingham, AL, USA.

Nishtha Sodhi (N)

University of Virginia Health System, Charlottesville, VA, USA.

Younghoon Kwon (Y)

University of Washington Medical Center, Seattle, WA, USA.

Salpy V Pamboukian (SV)

University of Alabama at Birmingham, Birmingham, AL, USA.

Philip B Adamson (PB)

Global Research and Development, St. Jude Medical, Sylmar, CA, USA.

Kenneth C Bilchick (KC)

University of Virginia Health System, Charlottesville, VA, USA.

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Classifications MeSH