Background
We have investigated the use of nebulized surfactant as a potential therapeutic option for the patients with coronavirus disease 2019 (COVID-19)-associated acute respiratory distress syndrome (ARDS) undergoing non-invasive ventilation.
Methods
The patients were divided into 2 groups: surfactant (n = 33) and control (n = 32). The subjects in the surfactant group received the inhaled surfactant at daily dose of 150–300 mg. The oxygenation parameters and several clinical outcomes were analyzed.
Results
On the 5 day of therapy, PaO
2
/FiO
2
improved significantly in the surfactant group compared to the control group (184 (155–212) mmHg
vs
150 (91–173) mmHg, p = 0.02). The inhaled surfactant significantly reduced the need for transfer of patients to intensive care units (24.2%
vs
46.9%, p = 0.05) and invasive mechanical ventilation (18.2%
vs
40.6%, p = 0.04). Even more, the nebulized surfactant shortened the length of non-invasive ventilation (7 (3–13) days
vs
11 (5–22) days, p = 0.02) and time spent in hospital (18 (16–27) days
vs
26 (21–31) days, p = 0.003) in patients suffering from COVID-19-linked ARDS.
Conclusions
Our preliminary data provided indications that inhaled surfactant therapy may represent a promising option for patients with COVID-19-associated ARDS. However, larger clinical trials are crucially needed.