Nebulized Heparin in Burn Patients with Inhalation Trauma-Safety and Feasibility.

burn heparin inhalation trauma nebulization safety

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
25 Mar 2020
Historique:
received: 12 03 2020
accepted: 20 03 2020
entrez: 29 3 2020
pubmed: 29 3 2020
medline: 29 3 2020
Statut: epublish

Résumé

Pulmonary hypercoagulopathy is intrinsic to inhalation trauma. Nebulized heparin could theoretically be beneficial in patients with inhalation injury, but current data are conflicting. We aimed to investigate the safety, feasibility, and effectiveness of nebulized heparin. International multicenter, double-blind, placebo-controlled randomized clinical trial in specialized burn care centers. Adult patients with inhalation trauma received nebulizations of unfractionated heparin (25,000 international unit (IU), 5 mL) or placebo (0.9% NaCl, 5 mL) every four hours for 14 days or until extubation. The primary outcome was the number of ventilator-free days at day 28 post-admission. Here, we report on the secondary outcomes related to safety and feasibility. The study was prematurely stopped after inclusion of 13 patients (heparin In this prematurely stopped trial, we encountered important safety and feasibility issues related to frequent heparin nebulizations in burn patients with inhalation trauma. This should be taken into account when heparin nebulizations are considered in these patients.

Sections du résumé

BACKGROUND BACKGROUND
Pulmonary hypercoagulopathy is intrinsic to inhalation trauma. Nebulized heparin could theoretically be beneficial in patients with inhalation injury, but current data are conflicting. We aimed to investigate the safety, feasibility, and effectiveness of nebulized heparin.
METHODS METHODS
International multicenter, double-blind, placebo-controlled randomized clinical trial in specialized burn care centers. Adult patients with inhalation trauma received nebulizations of unfractionated heparin (25,000 international unit (IU), 5 mL) or placebo (0.9% NaCl, 5 mL) every four hours for 14 days or until extubation. The primary outcome was the number of ventilator-free days at day 28 post-admission. Here, we report on the secondary outcomes related to safety and feasibility.
RESULTS RESULTS
The study was prematurely stopped after inclusion of 13 patients (heparin
CONCLUSION CONCLUSIONS
In this prematurely stopped trial, we encountered important safety and feasibility issues related to frequent heparin nebulizations in burn patients with inhalation trauma. This should be taken into account when heparin nebulizations are considered in these patients.

Identifiants

pubmed: 32218127
pii: jcm9040894
doi: 10.3390/jcm9040894
pmc: PMC7230289
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Nederlandse Brandwonden Stichting
ID : 12.001

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Gerie J Glas (GJ)

Laboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.
Department of Anesthesiology, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Janneke Horn (J)

Laboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.
Department of Intensive Care, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Jan M Binnekade (JM)

Department of Intensive Care, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Markus W Hollmann (MW)

Laboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.
Department of Anesthesiology, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Jan Muller (J)

Department of Intensive Care, University Hospital Gasthuisberg, 3000 Leuven, Belgium.

Berry Cleffken (B)

Department of Intensive Care, Maasstad Hospital, 3079 DZ Rotterdam, The Netherlands.

Kirsten Colpaert (K)

Department of Intensive Care, Ghent University Hospital, 9000 Ghent, Belgium.

Barry Dixon (B)

Department of Intensive Care, St Vincent's Hospital, Melbourne 3065, Australia.

Nicole P Juffermans (NP)

Laboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.
Department of Intensive Care, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Paul Knape (P)

Department of Intensive Care, Red Cross Hospital, 1942 LE Beverwijk, The Netherlands.

Marcel M Levi (MM)

Department of Vascular Medicine, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Bert G Loef (BG)

Department of Intensive Care, Martini Hospital, 9728 NT Groningen, The Netherlands.

David P Mackie (DP)

Department of Intensive Care, Red Cross Hospital, 1942 LE Beverwijk, The Netherlands.

Manu L N G Malbrain (MLNG)

Department of Intensive Care and Faculty of Medicine and Pharmacy, University Hospital Brussels, Jette, Belgium and Free University of Brussels, 1090 Brussels, Belgium.

Benedikt Preckel (B)

Laboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.
Department of Anesthesiology, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Auke C Reidinga (AC)

Department of Intensive Care, Martini Hospital, 9728 NT Groningen, The Netherlands.

K F van der Sluijs (KF)

Laboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Marcus J Schultz (MJ)

Laboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.
Department of Intensive Care, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.

Classifications MeSH