This analysis was based on the INHALE-HEP mate-trial (NCT04635241) [1], which Prof. Frank van Haren (St George Hospital, Australia) describe as “ a prospective pooled analysis of individual, de-identified patient-level data from multiple individual trials.” Trials were eligible if they were prospective, controlled, included an inhaled nebulised unfractionated heparin arm, and included adult patients hospitalised with confirmed COVID-19. Patients were excluded if they were intubated or required immediate intubation. In total, 6 trials with 478 participants were included [2].
Inhaled nebulised heparin showed a significant improvement in the primary outcome of intubation or death. 11.2% of participants receiving nebulised unfractionated heparin versus 22.4% of control participants reached the primary endpoint, corresponding to an OR of 0.43 (95% CI 0.26-0.73; P=0.001). Nebulised heparin also improved secondary outcomes, including intubation alone, in-hospital mortality, 28-day mortality, and hospital length of stay. No major bleeding, pulmonary bleeding, or heparin-induced thrombocytopenia were reported.
“In this meta-trial of 478 participants who were not intubated at baseline, inhaled nebulised unfractionated heparin was safe and significantly reduced intubation and mortality rates”, concluded Prof. van Haren.
- van Haren F, et al. Br J Clin Pharmacol. 2021;87(8):3075-3091.
- van Haren F, et al. Efficacy of inhaled nebulised unfractionated heparin to prevent intubation or death in hospitalised patients with COVID-19: a prospective international meta-trial of randomised clinical studies. ERS Congress, 27 September–1 October 2025, Amsterdam, The Netherlands.
Medical writing support was provided by Mihai Surducan, PhD.
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Table of Contents: ERS 2025
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