Severe COVID-19 ARDS Treated by Bronchoalveolar Lavage with Diluted Exogenous Pulmonary Surfactant as Salvage Therapy: In Pursuit of the Holy Grail?
COVID-19
acute respiratory distress syndrome (ARDS)
coronavirus disease
non-invasive respiratory support (NIRS)
respiratory failure
surfactant
Journal
Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588
Informations de publication
Date de publication:
21 Jun 2022
21 Jun 2022
Historique:
received:
28
05
2022
revised:
18
06
2022
accepted:
20
06
2022
entrez:
9
7
2022
pubmed:
10
7
2022
medline:
10
7
2022
Statut:
epublish
Résumé
Severe pneumonia caused by coronavirus disease 2019 (COVID-19) is characterized by inflammatory lung injury, progressive parenchymal stiffening and consolidation, alveolar and airway collapse, altered vascular permeability, diffuse alveolar damage, and surfactant deficiency. COVID-19 causes both pneumonia and acute respiratory distress syndrome (COVID-19 ARDS). COVID-19 ARDS is characterized by severe refractory hypoxemia and high mortality. Despite extensive research, the treatment of COVID-19 ARDS is far from satisfactory. Some treatments are recommended for exhibiting some clinically positive impacts on COVID-19 patients although there are already several drugs in clinical trials, some of which are already demonstrating promising results in addressing COVID-19. Few studies have demonstrated beneficial effects in non-COVID-19 ARDS treatment of exogenous surfactant, and there is no evidence-based, proven method for the procedure of surfactant administration. The aim of this work is to underline the key role of ATII cells and reduced surfactant levels in COVID-19 ARDS and to emphasize the rational basis for exogenous surfactant therapy in COVID-19 ARDS, providing insights for future research. In this article, we describe and support via the literature the decision to administer large volumes of surfactant to two patients via bronchoalveolar lavage to maximize its distribution in the respiratory tract. In this study, we report on two cases of COVID-19 ARDS in patients who have been successfully treated with diluted surfactants by bronchoalveolar lavage, followed by a low-dose bolus of surfactant. Combining the administration of diluted, exogenous pulmonary surfactant via bronchoalveolar lavage along with the standard therapy for SARS-CoV-2-induced ARDS may be a promising way of improving the management of ARDS.
Sections du résumé
BACKGROUND
BACKGROUND
Severe pneumonia caused by coronavirus disease 2019 (COVID-19) is characterized by inflammatory lung injury, progressive parenchymal stiffening and consolidation, alveolar and airway collapse, altered vascular permeability, diffuse alveolar damage, and surfactant deficiency. COVID-19 causes both pneumonia and acute respiratory distress syndrome (COVID-19 ARDS). COVID-19 ARDS is characterized by severe refractory hypoxemia and high mortality. Despite extensive research, the treatment of COVID-19 ARDS is far from satisfactory. Some treatments are recommended for exhibiting some clinically positive impacts on COVID-19 patients although there are already several drugs in clinical trials, some of which are already demonstrating promising results in addressing COVID-19. Few studies have demonstrated beneficial effects in non-COVID-19 ARDS treatment of exogenous surfactant, and there is no evidence-based, proven method for the procedure of surfactant administration.
AIM
OBJECTIVE
The aim of this work is to underline the key role of ATII cells and reduced surfactant levels in COVID-19 ARDS and to emphasize the rational basis for exogenous surfactant therapy in COVID-19 ARDS, providing insights for future research.
METHODS
METHODS
In this article, we describe and support via the literature the decision to administer large volumes of surfactant to two patients via bronchoalveolar lavage to maximize its distribution in the respiratory tract.
RESULTS
RESULTS
In this study, we report on two cases of COVID-19 ARDS in patients who have been successfully treated with diluted surfactants by bronchoalveolar lavage, followed by a low-dose bolus of surfactant.
CONCLUSION
CONCLUSIONS
Combining the administration of diluted, exogenous pulmonary surfactant via bronchoalveolar lavage along with the standard therapy for SARS-CoV-2-induced ARDS may be a promising way of improving the management of ARDS.
Identifiants
pubmed: 35806862
pii: jcm11133577
doi: 10.3390/jcm11133577
pmc: PMC9267619
pii:
doi:
Types de publication
Journal Article
Langues
eng
Références
Respir Med. 2021 Jan;176:106239
pubmed: 33246294
Postgrad Med J. 2020 Jul;96(1137):403-407
pubmed: 32522846
Tomography. 2022 Apr 24;8(3):1221-1227
pubmed: 35645386
ERJ Open Res. 2021 Aug 23;7(3):
pubmed: 34435038
Eur Respir J. 2020 Apr 16;55(4):
pubmed: 32269085
J Cardiothorac Vasc Anesth. 2012 Oct;26(5):849-56
pubmed: 22265270
Intensive Care Med. 1998 May;24(5):494-500
pubmed: 9660267
ACS Nano. 2020 Nov 25;:
pubmed: 33236896
Respir Res. 2021 Jan 18;22(1):20
pubmed: 33461535
Crit Care. 2012 Nov 22;16(6):238
pubmed: 23171712
Rheumatology (Oxford). 2022 Apr 11;61(4):1600-1609
pubmed: 34320649
Expert Rev Respir Med. 2021 May;15(5):597-608
pubmed: 33331197
Pediatr Pulmonol. 2001 Apr;31(4):317-20
pubmed: 11288218
Physiol Res. 2021 Dec 16;70(S2):S195-S208
pubmed: 34913352
JAMA Pediatr. 2014 Oct;168(10):901-8
pubmed: 25089718
J Clin Med. 2022 Mar 19;11(6):
pubmed: 35330029
Respir Physiol Neurobiol. 2021 Jun;288:103645
pubmed: 33657448
Annu Rev Physiol. 2003;65:613-42
pubmed: 12517997
Front Biosci (Landmark Ed). 2021 Dec 30;26(12):1607-1612
pubmed: 34994174
J Clin Med. 2022 May 24;11(11):
pubmed: 35683340
Int J Mol Sci. 2021 Mar 04;22(5):
pubmed: 33806395
J Mater Chem B. 2021 Sep 15;9(35):6988-6993
pubmed: 34085075
Drug Des Devel Ther. 2013 Aug 29;7:905-16
pubmed: 24039400
Sci Rep. 2020 Nov 10;10(1):19395
pubmed: 33173052
J Genet. 2021;100:
pubmed: 33707363
J Pharm Anal. 2022 Apr;12(2):215-220
pubmed: 34934510
Exp Ther Med. 2017 Sep;14(3):2608-2612
pubmed: 28947918
Respir Res. 2019 Nov 6;20(1):245
pubmed: 31694668
Am J Respir Crit Care Med. 2021 Nov 1;204(9):1024-1034
pubmed: 34449302
J Clin Med. 2022 Mar 09;11(6):
pubmed: 35329813
Intensive Care Med. 2020 Dec;46(12):2284-2296
pubmed: 33150472
J Clin Med. 2021 Sep 02;10(17):
pubmed: 34501430
J Clin Med. 2022 Mar 16;11(6):
pubmed: 35329965
Eur Respir J. 2020 Oct 8;56(4):
pubmed: 32764117
Anaesthesist. 1997 Nov;46(11):969-73
pubmed: 9490585
Open Forum Infect Dis. 2020 Sep 12;7(10):ofaa421
pubmed: 33072814
Exp Ther Med. 2013 Jan;5(1):237-242
pubmed: 23251275
Int J Mol Sci. 2020 Nov 20;21(22):
pubmed: 33233715
Trials. 2020 Dec 10;21(1):1014
pubmed: 33302976