Quality of Life 3 and 12 Months Following Acute Pulmonary Embolism: Analysis From a Prospective Multicenter Cohort Study.


Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
06 2021
Historique:
received: 21 08 2020
revised: 11 01 2021
accepted: 14 01 2021
pubmed: 7 2 2021
medline: 21 10 2021
entrez: 6 2 2021
Statut: ppublish

Résumé

Few data are available on the long-term course and predictors of quality of life (QoL) following acute pulmonary embolism (PE). What are the kinetics and determinants of disease-specific and generic health-related QoL 3 and 12 months following an acute PE? The Follow-up after Acute Pulmonary Embolism (FOCUS) study prospectively followed up consecutive adult patients with objectively diagnosed PE. Patients were considered for study who completed the Pulmonary Embolism Quality of Life (PEmb-QoL) questionnaire at predefined visits 3 and 12 months following PE. The course of disease-specific QoL as assessed using the PEmb-QoL and the impact of baseline characteristics using multivariable mixed effects linear regression were studied; also assessed was the course of generic QoL as evaluated by using the EuroQoL Group 5-Dimension 5-Level utility index and the EuroQoL Visual Analog Scale. In 620 patients (44% women; median age, 62 years), overall disease-specific QoL improved from 3 to 12 months, with a decrease in the median PEmb-QoL score from 19.4% to 13.0% and a mean individual change of -4.3% (95% CI, -3.2 to -5.5). Female sex, cardiopulmonary disease, and higher BMI were associated with worse QoL at both 3 and 12 months. Over time, the association with BMI became weaker, whereas older age and previous VTE were associated with worsening QoL. Generic QoL also improved: the mean ± SD EuroQoL Group 5-Dimension 5-Level utility index increased from 0.85 ± 0.22 to 0.87 ± 0.20 and the visual analog scale from 72.9 ± 18.8 to 74.4 ± 19.1. In a large cohort of survivors of acute PE, the change of QoL was quantified between months 3 and 12 following diagnosis, and factors independently associated with lower QoL and slower recovery of QoL were identified. This information may facilitate the planning and interpretation of clinical trials assessing QoL and help guide patient management. German Clinical Trials Registry (Deutsches Register Klinischer Studien: www.drks.de); No.: DRKS00005939.

Sections du résumé

BACKGROUND
Few data are available on the long-term course and predictors of quality of life (QoL) following acute pulmonary embolism (PE).
RESEARCH QUESTION
What are the kinetics and determinants of disease-specific and generic health-related QoL 3 and 12 months following an acute PE?
STUDY DESIGN AND METHODS
The Follow-up after Acute Pulmonary Embolism (FOCUS) study prospectively followed up consecutive adult patients with objectively diagnosed PE. Patients were considered for study who completed the Pulmonary Embolism Quality of Life (PEmb-QoL) questionnaire at predefined visits 3 and 12 months following PE. The course of disease-specific QoL as assessed using the PEmb-QoL and the impact of baseline characteristics using multivariable mixed effects linear regression were studied; also assessed was the course of generic QoL as evaluated by using the EuroQoL Group 5-Dimension 5-Level utility index and the EuroQoL Visual Analog Scale.
RESULTS
In 620 patients (44% women; median age, 62 years), overall disease-specific QoL improved from 3 to 12 months, with a decrease in the median PEmb-QoL score from 19.4% to 13.0% and a mean individual change of -4.3% (95% CI, -3.2 to -5.5). Female sex, cardiopulmonary disease, and higher BMI were associated with worse QoL at both 3 and 12 months. Over time, the association with BMI became weaker, whereas older age and previous VTE were associated with worsening QoL. Generic QoL also improved: the mean ± SD EuroQoL Group 5-Dimension 5-Level utility index increased from 0.85 ± 0.22 to 0.87 ± 0.20 and the visual analog scale from 72.9 ± 18.8 to 74.4 ± 19.1.
INTERPRETATION
In a large cohort of survivors of acute PE, the change of QoL was quantified between months 3 and 12 following diagnosis, and factors independently associated with lower QoL and slower recovery of QoL were identified. This information may facilitate the planning and interpretation of clinical trials assessing QoL and help guide patient management.
CLINICAL TRIAL REGISTRATION
German Clinical Trials Registry (Deutsches Register Klinischer Studien: www.drks.de); No.: DRKS00005939.

Identifiants

pubmed: 33548221
pii: S0012-3692(21)00242-7
doi: 10.1016/j.chest.2021.01.071
pii:
doi:

Banques de données

DRKS
['DRKS00005939']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2428-2438

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Luca Valerio (L)

Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Stefano Barco (S)

Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University, Mainz, Germany; Clinic of Angiology, University Hospital Zurich, Zurich, Switzerland.

Marius Jankowski (M)

Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Stephan Rosenkranz (S)

Department of Cardiology, Heart Center at the University Hospital Cologne, and Cologne Cardiovascular Research Center, Cologne, Germany.

Mareike Lankeit (M)

Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Matthias Held (M)

Abteilung für Innere Medizin, Missionsärztliche Klinik Würzburg, Würzburg, Germany.

Felix Gerhardt (F)

Department of Cardiology, Heart Center at the University Hospital Cologne, and Cologne Cardiovascular Research Center, Cologne, Germany.

Leonhard Bruch (L)

Klinik für Innere Medizin und Kardiologie, Unfallkrankenhaus Berlin, Berlin, Germany.

Ralf Ewert (R)

Department for Internal Medicine, Greifswald University Hospital, Greifswald, Germany.

Martin Faehling (M)

Klinik für Kardiologie, Angiologie und Pneumologie, Klinikum Esslingen, Esslingen am Neckar, Germany.

Julia Freise (J)

Klinik für Pneumologie, Medizinische Hochschule Hannover, Member of the German Center for Lung Research (DZL), Hannover, Germany.

Hossein-Ardeschir Ghofrani (HA)

Lung Center at the University of Giessen and Marburg, Member of the German Center for Lung Research (DZL), Marburg, Germany; Department of Medicine, Imperial College London, London, England.

Ekkehard Grünig (E)

Center for Pulmonary Hypertension, Thoraxklinik at Heidelberg University Hospital, Heidelberg, Germany.

Michael Halank (M)

Medizinische Klinik und Poliklinik I, Universitätsklinikum an der TU Dresden, Dresden, Germany.

Marius M Hoeper (MM)

Klinik für Pneumologie, Medizinische Hochschule Hannover, Member of the German Center for Lung Research (DZL), Hannover, Germany.

Frederikus A Klok (FA)

Department of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, The Netherlands.

Hanno H Leuchte (HH)

Department of Internal Medicine II, Neuwittelsbach Academic Hospital, Ludwig Maximilians University, Member of the DZL, Munich, Germany.

Eckhard Mayer (E)

Department of Thoracic Surgery, Kerckhoff Heart and Lung Center, Bad Nauheim, Germany.

F Joachim Meyer (FJ)

Lungenzentrum München, Klinik für Pneumologie und Pneumologische Onkologie, Klinikum Bogenhausen, Munich, Germany.

Claus Neurohr (C)

Medizinische Klinik und Poliklinik, LMU Klinikum der Universität München, Munich, Germany.

Christian Opitz (C)

Klinik für Innere Medizin, DRK Kliniken Berlin Westend, Berlin, Germany.

Kai-Helge Schmidt (KH)

Center for Cardiology, Cardiology 1, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Hans-Jürgen Seyfarth (HJ)

Department of Pneumology, Universitätsklinikum Leipzig AöR, Leipzig, Germany.

Franziska Trudzinski (F)

Saarland University Medical Center, Homburg, Germany; Pneumology and Critical Care Medicine at University Hospital Heidelberg, Translational Lung Research Center Heidelberg (TLRC), Member of German Center for Lung Research (DZL), Heidelberg, Germany.

Rolf Wachter (R)

Klinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig AöR, Leipzig, Germany.

Heinrike Wilkens (H)

Saarland University Medical Center, Homburg, Germany.

Philipp S Wild (PS)

Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University, Mainz, Germany; Preventive Cardiology and Preventive Medicine, Center for Cardiology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany; German Center for Cardiovascular Research (DZHK), Partner Site RheinMain, Mainz, Germany.

Stavros V Konstantinides (SV)

Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University, Mainz, Germany; Department of Cardiology, Democritus University of Thrace, Alexandroupolis, Greece. Electronic address: stavros.konstantinides@unimedizin-mainz.de.

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