The effect of intermittent pneumatic compression on deep-vein thrombosis and ventilation-free days in critically ill patients with heart failure.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
20 05 2022
Historique:
received: 31 10 2021
accepted: 03 05 2022
entrez: 20 5 2022
pubmed: 21 5 2022
medline: 25 5 2022
Statut: epublish

Résumé

There are contradictory data regarding the effect of intermittent pneumatic compression (IPC) on the incidence of deep-vein thrombosis (DVT) and heart failure (HF) decompensation in critically ill patients. This study evaluated the effect of adjunctive use of IPC on the rate of incident DVT and ventilation-free days among critically ill patients with HF. In this pre-specified secondary analysis of the PREVENT trial (N = 2003), we compared the effect of adjunctive IPC added to pharmacologic thromboprophylaxis (IPC group), with pharmacologic thromboprophylaxis alone (control group) in critically ill patients with HF. The presence of HF was determined by the treating teams according to local practices. Patients were stratified according to preserved (≥ 40%) versus reduced (< 40%) left ventricular ejection fraction, and by the New York Heart Association (NYHA) classification. The primary outcome was incident proximal lower-limb DVT, determined with twice weekly venous Doppler ultrasonography. As a co-primary outcome, we evaluated ventilation-free days as a surrogate for clinically important HF decompensation. Among 275 patients with HF, 18 (6.5%) patients had prevalent proximal lower-limb DVT (detected on trial day 1 to 3). Of 257 patients with no prevalent DVT, 11/125 (8.8%) patients in the IPC group developed incident proximal lower-limb DVT compared to 6/132 (4.5%) patients in the control group (relative risk, 1.94; 95% confidence interval, 0.74-5.08, p = 0.17). There was no significant difference in ventilator-free days between the IPC and control groups (median 21 days versus 25 days respectively, p = 0.17). The incidence of DVT with IPC versus control was not different across NYHA classes (p value for interaction = 0.18), nor across patients with reduced and preserved ejection fraction (p value for interaction = 0.15). Ventilator-free days with IPC versus control were also not different across NYHA classes nor across patients with reduced or preserved ejection fraction. In conclsuion, the use of adjunctive IPC compared with control was associated with similar rate of incident proximal lower-limb DVT and ventilator-free days in critically ill patients with HF.Trial registration: The PREVENT trial is registered at ClinicalTrials.gov, ID: NCT02040103 (registered on 3 November 2013, https://clinicaltrials.gov/ct2/show/study/NCT02040103 ) and Current controlled trials, ID: ISRCTN44653506 (registered on 30 October 2013).

Identifiants

pubmed: 35595804
doi: 10.1038/s41598-022-12336-9
pii: 10.1038/s41598-022-12336-9
pmc: PMC9122920
doi:

Substances chimiques

Anticoagulants 0

Banques de données

ClinicalTrials.gov
['NCT02040103']
ISRCTN
['ISRCTN44653506']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

8519

Informations de copyright

© 2022. The Author(s).

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Auteurs

Hasan M Al-Dorzi (HM)

Intensive Care Department, Ministry of National Guard Health Affairs, Riyadh, Kingdom of Saudi Arabia.
King Abdullah International Medical Research Center, Riyadh, Kingdom of Saudi Arabia.
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia.

Abdulaziz Al-Dawood (A)

Intensive Care Department, Ministry of National Guard Health Affairs, Riyadh, Kingdom of Saudi Arabia.
King Abdullah International Medical Research Center, Riyadh, Kingdom of Saudi Arabia.
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia.

Fahad M Al-Hameed (FM)

Intensive Care Department, Ministry of National Guard Health Affairs, Jeddah, Kingdom of Saudi Arabia.
King Abdullah International Medical Research Center Jeddah, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia.

Karen E A Burns (KEA)

Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Canada.
Unity Health Toronto - St Michael's Hospital, Toronto, Canada.
Li Ka Shing Knowledge Institute, Toronto, Canada.

Sangeeta Mehta (S)

Department of Medicine, Medical Surgical ICU, Mount Sinai Hospital, University of Toronto, Toronto, Canada.

Jesna Jose (J)

Department Biostatistics and Bioinformatics, King Abdullah International Medical Research Center, Riyadh, Kingdom of Saudi Arabia.
King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia.

Sami Alsolamy (S)

Intensive Care Department, Ministry of National Guard Health Affairs, Riyadh, Kingdom of Saudi Arabia.
King Abdullah International Medical Research Center, Riyadh, Kingdom of Saudi Arabia.
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia.

Sheryl Ann I Abdukahil (SAI)

Intensive Care Department, Ministry of National Guard Health Affairs, Riyadh, Kingdom of Saudi Arabia.
King Abdullah International Medical Research Center, Riyadh, Kingdom of Saudi Arabia.
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia.

Lara Y Afesh (LY)

King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia.
Research Office, King Abdullah International Medical Research Center, Riyadh, Kingdom of Saudi Arabia.

Mohammed S Alshahrani (MS)

Department of Emergency and Critical Care Medicine, College of Medicine, King Fahd Hospital of the University-Imam Abdulrahman Bin Faisal University, Dammam, Kingdom of Saudi Arabia.

Yasser Mandourah (Y)

Military Medical Services, Ministry of Defense, Riyadh, Kingdom of Saudi Arabia.

Ghaleb A Almekhlafi (GA)

Department of Intensive Care Services, Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia.

Mohammed Almaani (M)

Department of Pulmonary and Critical Care Medicine, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia.

Ali Al Bshabshe (A)

Department of Critical Care Medicine, Asir Central Hospital, King Khalid University, Abha, Kingdom of Saudi Arabia.

Simon Finfer (S)

The George Institute for Global Health, University of New South Wales, Sydney, Australia.

Zia Arshad (Z)

Department of Anesthesiology and Critical Care, King George's Medical University, Lucknow, India.

Imran Khalid (I)

Critical Care Section, Department of Medicine, King Faisal Specialist Hospital and Research Center, Jeddah, Kingdom of Saudi Arabia.

Yatin Mehta (Y)

Institute of Critical Care and Anaesthesiology, Medanta - The Medicity, Gurgaon, Haryana, India.

Atul Gaur (A)

Intensive Care Department, Gosford Hospital, Gosford, New South Wales, Australia.

Hassan Hawa (H)

Critical Care Medicine Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.

Hergen Buscher (H)

Department of Intensive Care Medicine, Centre for Applied Medical Research, St. Vincent's Hospital, University of New South Wales, Sydney, Australia.

Hani Lababidi (H)

Department of Pulmonary and Critical Care Medicine, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia.

Abdulsalam Al Aithan (A)

Intensive Care Division, Department of Medicine, King Abdulaziz Hospital, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, Al Ahsa, Kingdom of Saudi Arabia.

Yaseen M Arabi (YM)

Intensive Care Department, Ministry of National Guard Health Affairs, Riyadh, Kingdom of Saudi Arabia. yaseenarabi@yahoo.com.
King Abdullah International Medical Research Center, Riyadh, Kingdom of Saudi Arabia. yaseenarabi@yahoo.com.
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia. yaseenarabi@yahoo.com.

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