Nebulized in-line endotracheal dornase alfa and albuterol administered to mechanically ventilated COVID-19 patients: a case series

Abstract Background Mechanically ventilated patients with COVID-19 have a mortality of 24-53%, in part due to distal mucopurulent secretions interfering with ventilation. DNA from neutrophil extracellular traps (NETs) contribute to the viscosity of mucopurulent secretions and NETs are found in the s...

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Main Authors: Andrew G. Weber (Author), Alice S. Chau (Author), Mikala Egeblad (Author), Betsy J. Barnes (Author), Tobias Janowitz (Author)
Format: Book
Published: BMC, 2020-09-01T00:00:00Z.
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001 doaj_ea3656d9d7df4a9fa2ca0e4e0b30b0f1
042 |a dc 
100 1 0 |a Andrew G. Weber  |e author 
700 1 0 |a Alice S. Chau  |e author 
700 1 0 |a Mikala Egeblad  |e author 
700 1 0 |a Betsy J. Barnes  |e author 
700 1 0 |a Tobias Janowitz  |e author 
245 0 0 |a Nebulized in-line endotracheal dornase alfa and albuterol administered to mechanically ventilated COVID-19 patients: a case series 
260 |b BMC,   |c 2020-09-01T00:00:00Z. 
500 |a 10.1186/s10020-020-00215-w 
500 |a 1076-1551 
500 |a 1528-3658 
520 |a Abstract Background Mechanically ventilated patients with COVID-19 have a mortality of 24-53%, in part due to distal mucopurulent secretions interfering with ventilation. DNA from neutrophil extracellular traps (NETs) contribute to the viscosity of mucopurulent secretions and NETs are found in the serum of COVID-19 patients. Dornase alfa is recombinant human DNase 1 and is used to digest DNA in mucoid sputum. Here, we report a single-center case series where dornase alfa was co-administered with albuterol through an in-line nebulizer system. Methods Demographic and clinical data were collected from the electronic medical records of five mechanically ventilated patients with COVID-19-including three requiring veno-venous extracorporeal membrane oxygenation-treated with nebulized in-line endotracheal dornase alfa and albuterol, between March 31 and April 24, 2020. Data on tolerability and response were analyzed. Results The fraction of inspired oxygen requirements was reduced for all five patients after initiating dornase alfa administration. All patients were successfully extubated, discharged from hospital and remain alive. No drug-associated toxicities were identified. Conclusions Results suggest that dornase alfa will be well-tolerated by patients with severe COVID-19. Clinical trials are required to formally test the dosing, safety, and efficacy of dornase alfa in COVID-19, and several have been recently registered. 
546 |a EN 
690 |a SARS-CoV-2 
690 |a COVID-19 
690 |a Coronavirus 
690 |a Mucopurulent secretions 
690 |a Dornase alfa 
690 |a Neutrophil extracellular traps 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
690 |a Biochemistry 
690 |a QD415-436 
655 7 |a article  |2 local 
786 0 |n Molecular Medicine, Vol 26, Iss 1, Pp 1-7 (2020) 
787 0 |n http://link.springer.com/article/10.1186/s10020-020-00215-w 
787 0 |n https://doaj.org/toc/1076-1551 
787 0 |n https://doaj.org/toc/1528-3658 
856 4 1 |u https://doaj.org/article/ea3656d9d7df4a9fa2ca0e4e0b30b0f1  |z Connect to this object online.