Preview

Tuberculosis and Lung Diseases

Advanced search

Inhalation surfactant therapy in the integrated treatment of severe COVID-19 pneumonia

https://doi.org/10.21292/2075-1230-2020-98-9-6-12

Abstract

The objective: to evaluate the effectiveness of inhaled surfactant therapy in the integrated treatment of severe COVID-19 pneumonia in a multicenter prospective clinical trial of surfactant-BL.

Subjects and methods. 122 patients with severe COVID-19-associated pneumonia treated in two treatment centers were enrolled in the study. All of them received antiviral, anticoagulant and anti-inflammatory therapy. 56 patients also received inhalation therapy with surfactant-BL (OOO Biosurf, St. Petersburg, Russia) at a dose of 1 mg/kg 2-3 times a day. The remaining 66 patients received no surfactant-BL inhalation. When included into the study, all patients were divided into two groups based on severity of the condition at the time of inclusion: 62 people (Group I) needed oxygen inhalation through a face mask with the flow of 6-8 L/min for hypoxemia correction (27 received surfactant therapy and 35 did not); other 60 patients (Group II) required non-invasive respiratory support (constant positive airway pressure, non-invasive mechanical ventilation, high-flow oxygen therapy), of them 29 received surfactant therapy, while 31 patients did not.

Results. In Group I, switching to invasive mechanical ventilation was required for 3/27 (11.1%) patients who received surfactant therapy, and 10/35 (28.6%) who received no surfactant therapy (p = 0.085); lethality made 3/27 (11.1%) and 9/35 (25.7%) (p = 0.131), respectively. In Group II, among those who received surfactant therapy, 5/29 (17.2%) were switched to invasive mechanical ventilation and 18/31 (58.1%) among those who did not receive it (p = 0.001); lethality made 5/29 (17.2%) and 18/31 (58.1%) (p = 0.001), respectively. In the pooled group of 122 patients with severe COVID-19-associated pneumonia, 8 (14.3%) of 56 patients who received surfactant died, and 27 (40.9%) of 66 died among those who did not receive it, (p = 0.001).

Conclusion: Inhalation surfactant therapy can reduce the frequency of switching patients to mechanical ventilation and statistically significantly reduce lethality caused by severe pneumonia associated with SARS-CoV-2. 

About the Authors

A. E. Bautin
Almazov National Medical Research Center
Russian Federation

Head of Anesthesiology and Intensive Care Laboratory,

2, Akkuratova St., St. Petersburg, 197341



S. N. Avdeev
I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Doctor of Medical Sciences, Correspondent Member of the Russian Academy of Science, Professor, Head of Pulmonology Department,

Build. 1, 19 Bolshaya Pirogovskaya St., Moscow, 119146



A. A. Seyliev
A.M. Granov Russian Research Center of Radiology and Surgical Technologies
Russian Federation

Leading Researcher of Medical Biotechnological Laboratory,

70, Leningradskaya St., Settlement of Pesochny, St. Petersburg, 197758



M. V. Shvechkova
Perinatal Center
Russian Federation

Perinatal Center, Head of Intensive Care Department,

26, Energetikov St., Tyumen, 625023



Z. M. Merzhoeva
I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Candidate of Medical Sciences, Assistant of Pulmonology Department,

Build. 1, 19 Bolshaya Pirogovskaya St., Moscow, 119146



N. V. Trushenko
I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Candidate of Medical Sciences, Assistant of Pulmonology Department,

Build. 1, 19 Bolshaya Pirogovskaya St., Moscow, 119146



A. P. Semenov
Almazov National Medical Research Center
Russian Federation

Head of Cardiology Department no. 7,

2, Akkuratova St., St. Petersburg, 197341



K. B. Lapshin
Almazov National Medical Research Center
Russian Federation

Head of Anesthesiology and Intensive Care Department no. 14,

2, Akkuratova St., St. Petersburg, 197341



O. A. Rozenberg
A.M. Granov Russian Research Center of Radiology and Surgical Technologies
Russian Federation

Doctor of Medical Sciences, Professor, Head of Medical Biotechnological Laboratory,

70, Leningradskaya St., Settlement of Pesochny, St. Petersburg, 197758



References

1. Аlekseev А.M., Shupinskiy O.V., Khrapov K.N. Intensive care of patients with severe influenza A(H1N1) complicated by pneumonia. Messenger of Anesthesiology and Resuscitation, 2009, no. 6, pp. 35-38. (In Russ.)

2. Аlekseev А.M., Yakovlev А.А., Shvechkova M.V., Seyliev А.А., Volchkov V.А., Rozenberg O.А. Surfactant therapy for pneumonia and ARDS associated with the A/H1N1 virus. Zabaykalskiy Meditsinskiy Journal, 2011, no. 1, pp. 23-27. (In Russ.)

3. Bautin А.E., Osovskikh V.V., Khubulava G.G., Granov D.А., Kozlov I.А., Erokhin V.V., Likhvantsev V.V., Tsarenko S.V., Kazennov V.V., Zhilin Yu.N., Poptsov V.N., Shulga А.E., Kirillov Yu.А., Seyliev А.А., Volchkov V.А., Rozenberg O.А. Multi-center clinical trials of surfactant-BL for the treatment of respiratory distress syndrome of adults. Klinicheskie Issledovaniya Lekarstvennykh Sredstv v Rossii, 2002, no. 2, pp. 18-23. (In Russ.)

4. Rozenberg O.А., Danilov L.N., Volchkov V.А., Lebedeva E.S., Dubrovskaya V.F., Valkovich А.А., Klestova O.V., Kirillov Yu.А., Seyliev А.А., Shaldzhyan А.А., Loshakova L.V., Shulga А.E., Zhuykov А.G. Pharmacological properties and therapeutic activity of the Russian pulmonary surfactant. Bull. Eksperim. Biol. i Med., 1998, vol. 126, no. 10, pp. 455-458. (In Russ.)

5. Bautin A., Chubulava G., Kozlov I., Poptzov V., Osovskikh V., Seiliev A., Volchkov V. and Rosenberg O. Surfactant therapy for patients with ards after cardiac surgery. J. Liposome Research, 2006, vol. 16, no. 3, pp. 265-272.

6. Busani S., Girardis M., Biagioni E. Surfactant therapy and intravenous Zanamivir in severe respiratory failure due to persistent influenza A/H1N1 2009 virus infection. Am. J. Respir. Critical Care Mеd., 2010, vol. 182, no. 10, pp. 1334.

7. Fukushi M., Tohru M., Miyoshi-Akiyama, Kubo S., Yamamoto K., Kudo K. Laninamivir octanoate and artificial surfactant combination therapy significantly increases survival of mice infected with lethal influenza H1N1 virus. PLoS ONE, 2012, vol. 7, no. 8, pp. e42419. doi:10.1371/journal.pone.0042419.

8. Günther A., Siebert C., Schmidt R., Ziegler S., Grimminger F., Yabut M., Temmesfeld B., Walmrath D., Morr H., Seeger W. Surfactant alterations in severe pneumonia, ARDS and cardiogenic lung edema. Am. J. Resp. Crit. Care Med., 1996, vol. 153, no. 1, pp. 176-184. http://dx.doi.org/10.1164/ajrccm.153.1.8542113. PMID: 12030716.

9. Kula R., Maca J., Sklienka P., Szturz P., Jahoda S., Czerny D., Chulek V., Sukenik P. Exogenous surfactant as a component of complex non-ECMO therapy for ARDS caused by influenza A virus (2009 А1/Н1). Bratisl Lek Listy, 2011, no. 112, pp. 218-222.

10. Numata M., Kandasamy P., Nagashima Y., Posey J., Hartshorn K., Woodland D., Voelker D.R. Phosphatidylglycerol suppresses influenza A virus infection. Am. J. Respir.Cell. Mol. Biol., 2012, vol. 46, no. 4, pp. 479-487. doi: 10.1165/rcmb.2011-0194OC.

11. Rosenberg O.A., Bautin A.E., Osovskich V.V., Tsibulkin E.K., Gavrilin S.V., Kozlov I.A. When to start surfactant therapy (ST-thetrapy) of acute lung injury? Eur. Respir. J., 2001, vol. 18, suppl. 38, pp. 153, 7s. (11th ERS Annual Congress, Berlin).

12. Rosenberg O.A., Bautin A.E., Seiliev A.A. Late Start of surfactant therapy and surfactant drug composition as major causes of failure of phase III multi-center clinical trials of surfactant therapy in adults with ARDS. Intern. J. Biomedicine, 2018, no. 8, pp. 253-254.

13. Rosenberg O., Seiliev A., Zhuikov A. Lung surfactants: Correlation between biophysical characteristics, composition and therapeutic efficacy. In: Gregory Gregoriadis, ed., Liposome Technology, Informa Healthcare, Taylor&Francis Group, 2006, 3rd ed, Vol. III, Ch. 17, pp. 317-346.

14. Takano H. Pulmonary surfactant itself must be a strong defender against SARS-CoV-2. Medical Hypotheses, 2020, no. 144, 110020, pp. 1-2.

15. van Iwaarden F.J., van Golde L.M.J. Pulmonary surfactant and lung defense. In: Robertson B., Taeusch H.W. (eds.). Surfactant therapy for lung disease. Lung Biol. Health Dis., vol. 84, New York, Marcel Dekker Inc., 1995, pp. 75-84.

16. Vlasenko A., Osovskikh V., Tarasenko M., Rozenberg O. Efficiency of surfactant therapy for ALI/ARDS in homogenous nosologic groups of patients. Eur. Respir. J., 2005, vol. 26, suppl. 49, pp. 90.

17. Witczak A., Prystupa A., Kurys-Denis E. Acute respiratory distress syndrome (ARDS) complicating influenza A/H1N1v infection – a clinical approach. Ann. Agricultural Environmental Med., 2013, vol. 20, no. 4, pp. 820-822.


Review

For citations:


Bautin A.E., Avdeev S.N., Seyliev A.A., Shvechkova M.V., Merzhoeva Z.M., Trushenko N.V., Semenov A.P., Lapshin K.B., Rozenberg O.A. Inhalation surfactant therapy in the integrated treatment of severe COVID-19 pneumonia. Tuberculosis and Lung Diseases. 2020;98(9):6-12. (In Russ.) https://doi.org/10.21292/2075-1230-2020-98-9-6-12

Views: 3233


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2075-1230 (Print)
ISSN 2542-1506 (Online)