Preview

PULMONOLOGIYA

Advanced search

Federal guidelines on diagnosis and treatment of bronchial asthma

https://doi.org/10.18093/0869-0189-2022-32-3-393-447

Abstract

Bronchial asthma is a heterogeneous disease that requires identification of its phenotype and a personalized approach to therapy. At the same time, despite a wide range of therapeutic options, many patients with asthma cannot achieve control over the disease.

Methodology. The target audience of these clinical recommendations are general practitioners, therapists, pediatricians, allergologists-immunologists, pulmonologists, and functional diagnostics doctors. Each thesis-recommendation about diagnostic and therapeutic procedures has been scored according to the scales of classes of recommendations from 1 to 5 and A, B, C scale of the levels of evidence. The clinical recommendations also contain comments and explanations to the theses, algorithms for the diagnosis and treatment of bronchial asthma, and reference materials.

Conclusion. The presented clinical guidelines cover current information about the etiology and pathogenesis, classification, clinical manifestations, diagnosis, treatment, and prevention of bronchial asthma. These guidelines were approved by the Scientific and Practical Council of the Ministry of Health of the Russian Federation in 2021. 

About the Authors

A. G. Chuchalin
Pirogov Russian National Research Medical University (Pirogov Medical University), Ministry of Health of the Russian Federation
Russian Federation

Doctor of Medicine, Professor, Academician of Russian Academy of Sciences, Head of Department of Hospital Internal Medicine, Pediatric Faculty, ul. Ostrovityanova 1, Moscow, 117997;

Chairman of the Executive Board of Russian Respiratory Society



S. N. Avdeev
Federal State Autonomous Educational Institution of Higher Education I.M.Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University); Federal Pulmonology Research Institute, Federal Medical and Biological Agency of Russia
Russian Federation

Doctor of Medicine, Professor, Academician of Russian Academy of Sciences, Head of the Department of Pulmonology, N.V.Sklifosovsky Institute of Clinical Medicine, ul. Trubetskaya 8, build. 2, Moscow, 119991ж

Leading Researcher, Orehovyj bul’var 28, Moscow, 115682



Z. R. Aisanov
Pirogov Russian National Research Medical University (Pirogov Medical University), Ministry of Health of the Russian Federation
Russian Federation

Doctor of Medicine, Professor, Department of Pulmonology, 

ul. Ostrovityanova 1, Moscow, 117997



A. S. Belevskiy
Pirogov Russian National Research Medical University (Pirogov Medical University), Ministry of Health of the Russian Federation
Russian Federation

Doctor of Medicine, Professor, Head of the Department of Pulmonology, Faculty of Postgraduate Physician Training, 

ul. Ostrovityanova 1, Moscow, 117997



O. S. Vasil’eva
Federal Pulmonology Research Institute, Federal Medical and Biological Agency of Russia
Russian Federation

Doctor of Medicine, Professor, Head of Laboratory of Environmental and Occupational Pulmonary Diseases,

Orehovyj bul’var 28, Moscow, 115682



N. A. Geppe
Federal State Autonomous Educational Institution of Higher Education I.M.Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)
Russian Federation

Doctor of Medicine, Professor, Head of Department of Pediatric Diseases, Therapeutic Faculty, 

ul. Trubetskaya 8, build. 2, Moscow, 119991



G. L. Ignatova
South Ural State Medical University, Healthcare Ministry of Russia
Russian Federation

Doctor of Medicine, Professor, Head of Department of Therapy, Institute of Postgraduate Physician Training,

ul. Vorovskogo 64, Chelyabinsk, 454092

Head of the City Pulmonology Center (Chelyabinsk); Chief pulmonologist of Chelyabinsk



N. P. Knyazheskaya
Pirogov Russian National Research Medical University (Pirogov Medical University), Ministry of Health of the Russian Federation
Russian Federation

Candidate of Medicine, Associate Professor at Department of of Pulmonology, Faculty of Postgraduate Physician Training, 

ul. Ostrovityanova 1, Moscow, 117997



A. B. Malakhov
Federal State Autonomous Educational Institution of Higher Education I.M.Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)
Russian Federation

Doctor of Medicine, Professor at Department of Pediatric Diseases, 

ul. Trubetskaya 8, build. 2, Moscow, 119991



N. I. Meshcheryakova
Pirogov Russian National Research Medical University (Pirogov Medical University), Ministry of Health of the Russian Federation
Russian Federation

Candidate of Medicine, Associate Professor, Department of Pulmonology, Faculty of Postgraduate Physician Training, 

ul. Ostrovityanova 1, Moscow, 117997



N. M. Nenasheva
Russian Medical Academy of Continuous Professional Education, Healthcare Ministry of Russian Federation
Russian Federation

Doctor of Medicine, Professor, Department of Clinical Allergology,

ul. Barrikadnaya 2/1, build. 1, Moscow, 123995



R. S. Fassakhov
Federal State Autonomous Educational Institution of Higher Education “Kazan (Volga Region) Federal University” Ministry of Healthcare of the Russian Federation
Russian Federation

Doctor of Medicine, Professor, Department of Basic Clinical Medicine, 

ul. Kremlyovskaya 18, Kazan, 420008, Tatarstan Republic



R. M. Khaitov
Federal State Budgetary Educational Institution of the Higher Education “A.I.Yevdokimov Moscow State University of Medicine and Dentistry” of the Ministry of Healthcare of the Russian Federation; Federal Research Center “Institute of Immunology”, Federal Medical and Biological Agency of Russia
Russian Federation

Head of the Department of Immunology and Allergology, ul. Delegatskaya 20/1, Moscow, 127473;

Doctor of Medicine, Professor, Academician of the Russian Academy of Sciences, Scientific Director, Kashirskoe shosse 24, Moscow, 115478

 



N. I. Il’ina
Federal Research Center “Institute of Immunology”, Federal Medical and Biological Agency of Russia
Russian Federation

Doctor of Medicine, Professor, Deputy Director for Clinical Affairs, 

Kashirskoe shosse 24, Moscow, 115478



O. M. Kurbacheva
Federal Research Center “Institute of Immunology”, Federal Medical and Biological Agency of Russia
Russian Federation

Doctor of Medicine, Professor, Head of the Department of bronchial asthma, 

Kashirskoe shosse 24, Moscow, 115478



N. G. Astafieva
Saratov State Medical University named after V.I.Razumovsky, Healthcare Ministry of Russian Federation
Russian Federation

Doctor of Medicine, Professor, Head of the Department of Clinical Immunology and Allergology, 

ul. Bolshaya Kazachia 112, Saratov, 410012



I. V. Demko
Federal State Budgetary Educational Institution of Higher Education “Krasnoyarsk State Medical University named after Professor V.F.Voyno-Yasenetsky” of the Ministry of Health of the Russian Federation
Russian Federation

Doctor of Medicine, Professor, Head of Department of Internal Medicine No.2 with Postgraduate Physician Training Course, 

ul. Partizana Zheleznyaka 1, Krasnoyarsk, 660022



D. S. Fomina
Federal State Autonomous Educational Institution of Higher Education I.M.Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University); State Institution “City Hospital No.52”, Moscow Health Department
Russian Federation

Associate Professor, Department of Clinical Allergology аnd Immunology, ul. Trubetskaya 8, build. 2, Moscow, 119991;

Candidate of Medicine, Allergist and immunologist, Head of of diagnostic Division of Allergology аnd Immunology Center, Pekhotnaya ul. 3, Moscow, 123182 



L. S. Namazova-Baranova
Pirogov Russian National Research Medical University (Pirogov Medical University), Ministry of Health of the Russian Federation; Pediatrics and Child Health Research Institute of the “Central Clinical Hospital of the Russian Academy of Sciences”, Ministry of Education and Science of Russia
Russian Federation

Head of Faculty Pediatrics Department, Pediatric Faculty, ul. Ostrovityanova 1, Moscow,
117997;

Doctor of Medicine, Professor, Academician of the Russian Academy of Sciences, President of the Union of Pediatricians of Russia; Head of Pediatrics and Child Health Research Institute, ul. Fotievoy 10, buld. 1, Moscow, 119333;

Chief Pediatric Specialist in Preventive Medicine, Healthcare Ministry of Russia; Vice-President of the Global Pediatric Pulmonological Alliance



A. A. Baranov
Pediatrics and Child Health Research Institute of the “Central Clinical Hospital of the Russian Academy of Sciences”, Ministry of Education and Science of Russia
Russian Federation

Doctor of Medicine, Professor, Academician of the Russian Academy of Sciences, Honorary President of the Union of Russian Pediatricians; Chief Pediatrician of Healthcare Ministry of Russia; Manager’s adviser,

ul. Fotievoy 10, buld. 1, Moscow, 119333



E. A. Vishneva
Pirogov Russian National Research Medical University (Pirogov Medical University), Ministry of Health of the Russian Federation; Pediatrics and Child Health Research Institute of the “Central Clinical Hospital of the Russian Academy of Sciences”, Ministry of Education and Science of Russia
Russian Federation

Professor, Faculty Pediatrics Department, Pediatric Faculty, ul. Ostrovityanova 1, Moscow, 117997;

Doctor of Medicine, Press secretary of the Union of Russian Pediatricians, Deputy Director for Science, ul. Fotievoy 10, buld. 1, Moscow, 119333



G. A. Novik
Federal State budgetary Educational Institution of Higher Education “St. Petersburg State Pediatric Medical University” of the Ministry of Healthcare of the Russian Federation
Russian Federation

Doctor of Medicine, Professor, Head of I.M.Vorontsov Pediatric diseases Department, Faculty of Postgraduate and Additional Professional Education, 

ul. Litovskaya 2, Saint Petersburg, 194100



References

1. Global Initiative for Asthma. Global Strategy for Asthma Management and Prevention. Updated 2018. Available at: https://ginasthma.org/wp-content/uploads/2018/04/wms-GINA-2018-report-V1.3-002.pdf

2. Chuchalin A.G., Khaltaev N., Antonov N.S. Chronic respiratory diseases and risk factors in 12 regions of the Russian Federation. Int. J. Chron. Obstruct. Pulmon. Dis. 2014; 9 (1): 963-974. https://doi.org/10.2147/COPD.S67283.

3. Russian Respiratory Society. [National program “Bronchial asthma in children. Treatment strategy and prevention». 4rd edn. Moscow; 2012 (in Russian).

4. Centers for Disease Control and Prevention. Most recent asthma data. Available at: http://www.cdc.gov/asthma/most_recent_data.htm

5. Krahn M.D., Berka C., Langlois P., Detsky A.S. Direct and indirect costs of asthma in Canada, 1990. CMAJ. 1996; 154 (6): 821-831.

6. Weber E.J., Silverman R.A., Callaham M.L. et al. A prospective multicenter study factors associated with hospital admission among adults with acute asthma. Am. J. Med. 2002; 113 (5): 371-378. https://doi.org/10.1016/s0002-9343(02)01242-1.

7. Braman S.S., Kaermmerhen J.T. Intensive care of status asthmaticus: A 10-year experience. JAMA. 1990; 264 (3): 366-368. https://doi.org/10.1001/jama.1990.03450030090038.

8. Salmeron S., Liard R., Elkharrat D. et al. Asthma severity adequacy of management in accident and emergency departments in France: a prospective study. Lancet. 2001; 358 (9282): 629-635. https://doi.org/10.1016/s0140-6736(01)05779-8.

9. Krishnan V., Diette G.B., Rand C.S. et al. Mortality in patients hospitalized for asthma exacerbations in the United States. Am. J. Respir. Crit. Care Med. 2006; 174 (6): 633-638. https://doi.org/10.1164/rccm.200601-007OC.

10. Nenasheva N.M. [Clinical phenotypes of atopic bronchial asthma: diagnosis and treatment. Saarbrucken: Palmarium Academic Publishing; 2012 (in Russian).

11. Moore W.C., Meyers D.A., Wenzel S.E. et al. Identification of asthma phenotypes using cluster analysis in the severe asthma research program. Am. J. Respir. Crit. Care Med. 2010; 181 (4): 315-323. https://doi.org/10.1164/rccm.200906-0896OC.

12. Pearce N., Pekkanen J., Beasley R. How much asthma is really attributable to atopy? Thorax. 1999; 54 (3): 268-272. https://doi.org/10.1136/thx.54.3.268.

13. Mellis C. Respiratory noises: how useful are they clinically? Pediatr. Clin. North Am. 2009; 56 (1): 1-17. https://doi.org/10.1016/j.pcl.2008.10.003.

14. Cano Garcinuno A., Mora Gandarillas I., SLAM Study Group. Early patterns of wheezing in asthmatic and nonasthmatic children. Eur. Respir. J. 2013; 42 (4): 1020-1028. https://doi.org/10.1183/09031936.00148712.

15. Just J., Saint-Pierre P., Gouvis-Echraghi R. et al. Wheeze phenotypes in young children have different courses during the preschool period. Ann. Allergy Asthma Immunol. 2013; 111 (4): 256-261. https://doi.org/10.1016/j.anai.2013.07.002.

16. O’Byrne P.M., Reddel H.K., Eriksson G. et al. Measuring asthma control: a comparison of three classification systems. Eur. Respir. J. 2010; 36 (2): 269-276. https://doi.org/10.1183/09031936.00124009.

17. Thomas M., Kay S., Pike J. et al. The Asthma Control Test (ACT) as a predictor of GINA guideline-defined asthma control: analysis of a multinational cross-sectional survey. Prim. Care Respir. J. 2009; 18 (1): 41-49. https://doi.org/10.4104/pcrj.2009.00010.

18. Juniper E.F., Svensson K., Mörk A.C., Ståhl E. Measurement properties and interpretation of three shortened versions of the asthma control questionnaire. Respir. Med. 2005; 99 (5): 553-558. https://doi.org/10.1016/j.rmed.2004.10.008.

19. Kerkhof M., Tran T.N., van den Berge M. et al. Association between blood eosinophil count and risk of readmission for patients with asthma: Historical cohort study. PLoS One. 2018; 13 (7): e0201143. https://doi.org/10.1371/journal.pone.0201143.

20. Price D.B., Rigazio A., Campbell J.D. et al. Blood eosinophil count and prospective annual asthma disease burden: a UK cohort study. Lancet Respir. Med. 2015; 3 (11): 849-858. https://doi.org/10.1016/S2213-2600(15)00367-7.

21. Albers F.C., Licskai C., Chanez P. et al. Baseline blood eosinophil count as a predictor of treatment response to the licensed dose of mepolizumab in severe eosinophilic asthma. Respir. Med. 2019; 159: 105806. https://doi.org/10.1016/j.rmed.2019.105806.

22. Bush A. Management of asthma in children. Minerva Pediatr. 2018; 70 (5): 444-457. https://doi.org/10.23736/S0026-4946.18.05351-3.

23. Rath N., Raje N., Rosenwasser L. Immunoglobulin E as a biomarker in asthma. Immunol. Allergy Clin. North Am. 2018; 38 (4): 587-597. https://doi.org/10.1016/j.iac.2018.06.007.

24. Ahlstedt S., Murray C.S. In vitro diagnosis of allergy: how to interpret IgE antibody results in clinical practice. Prim. Care Respir. J. 2006; 15 (4): 228-236. https://doi.org/10.1016/j.pcrj.2006.05.004.

25. Miller M.R., Hankinson J., Brusasco V. et al. Standardisation of spirometry. Eur. Respir. J. 2005; 26 (2): 319-338. https://doi.org/10.1183/09031936.05.00034805.

26. Levy M.L., Quanjer P.H., Booker R. et al. Diagnostic spirometry in primary care: Proposed standards for general practice compliant with American Thoracic Society and European Respiratory Society recommendations. Prim. Care Respir. J. 2009; 18 (3): 130-147. https://doi.org/10.4104/pcrj.2009.00054.

27. Russian Respiratory Society. [Guidelines for the use of spirometry methods. Moscow; 2016. Available at: http://www.spulmo.ru (in Russian).

28. Pellegrino R., Viegi G., Brusasco V. et al. Interpretative strategies for lung function tests. Eur. Respir. J. 2005; 26 (5): 948-968. https://doi.org/10.1183/09031936.05.00035205.

29. Tan W.C., Vollmer W.M., Lamprecht B. et al. Worldwide patterns of bronchodilator responsiveness: results from the Burden of Obstructive Lung Disease study. Thorax. 2012; 67 (8): 718-726. https://doi.org/10.1136/thoraxjnl-2011-201445.

30. Crapo R.O., Casaburi R., Coates A.L. et al. Guidelines for methacholine and exercise challenge testing-1999. Am. J. Respir. Crit. Care Med. 2000; 161 (1): 309-329. https://doi.org/10.1164/ajrccm.161.1.ats11-99.

31. Swartz E., Lang D. When should a methacholine challenge be ordered for a patient with suspected asthma? Cleve Clin. J. Med. 2008; 75 (1): 37-40. https://doi.org/10.3949/ccjm.75.1.37.

32. Parsons J.P., Hallstrand T.S., Mastronarde J.G. et al. An official American Thoracic Society clinical practice guideline: exerciseinduced bronchoconstriction. Am. J. Respir. Crit. Care Med. 2013; 187 (9): 1016-1027. https://doi.org/10.1164/rccm.201303-0437ST.

33. Reddel H.K., Taylor D.R., Bateman E.D. et al. An official American Thoracic Society/European Respiratory Society statement: Asthma control and exacerbations: standardizing endpoints for clinical asthma trials and clinical practice. Am. J. Respir. Crit. Care Med. 2009; 180 (1): 59-99. https://doi.org/10.1164/rccm.200801-060ST.

34. Brouwer A.F., Brand P.L. Asthma education and monitoring: what has been shown to work. Paediatr. Respir. Rev. 2008; 9 (3): 193-199. https://doi.org/10.1016/j.prrv.2008.03.001.

35. Beydon N., Davis S.D., Lombardi E. et al. An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool children. Am. J. Respir. Crit. Care Med. 2007; 175 (12): 1304-1345. https://doi.org/10.1164/rccm.200605-642ST.

36. Graham B.L., Steenbruggen I., Miller M.R. et al. Standardization of spirometry 2019 update: An official American Thoracic Society and European Respiratory Society technical statement. Am. J. Respir. Crit. Care Med. 2019; 200 (8): e70-88. https://doi.org/10.1164/rccm.201908-1590ST.

37. American Thoracic Society, European Respiratory Society. ATS/ ERS Recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005. Am. J. Respir. Crit. Care Med. 2005; 171 (8): 912-930. https://doi.org/10.1164/rccm.200406-710ST.

38. Schleich F.N., Manise M., Sele J. et al. Distribution of sputum cellular phenotype in a large asthma cohort: predicting factors for eosinophilic vs neutrophilic inflammation. BMC Pulm. Med. 2013; 13: 11. https://doi.org/10.1186/1471-2466-13-11.

39. Dweik R.A., Boggs P.B., Erzurum S.C. et al. An official ATS clinical practice guideline: interpretation of exhaled nitric oxide levels (FENO) for clinical applications. Am. J. Respir. Crit. Care Med. 2011; 184 (5): 602-615. https://doi.org/10.1164/rccm.9120-11ST.

40. Malo J.L., Côte J., Cartier A. et al. How many times per day should peak expiratory flow rates be assessed when investigating occupational asthma? Thorax. 1993; 48 (12): 1211-1217. https://doi.org/10.1136/thx.48.12.1211.

41. Baur X., Huber H., Degens P.O. et al. Relation between occupational asthma case history, bronchial methacholine challenge, and specific challenge test in patients with suspected occupational asthma. Am. J. Ind. Med. 1998; 33 (2): 114-122. https://doi.org/10.1002/(sici)1097-0274(199802)33:2<114::aid-ajim3>3.0.co;2-y

42. Fishwick D., Barber C.M., Bradshaw L.M. et al. Standards of care for occupational asthma. Thorax. 2008; 63 (3): 240-250. https://doi.org/10.1136/thx.2007.083444.

43. Mapp C.E., Saetta M., Maestrelli P., Fabbri L. Occupational asthma. In: Mapp C.E., ed. Occupational Lung Disorders. European Respiratory Monograph. Sheffield: ERS; 1999; 4 (Monogr. 11): 255-285.

44. Bousquet J., Heinzerling L., Bachert C. et al. Practical guide to skin prick tests in allergy to aeroallergens. Allergy. 2012; 67 (1): 18-24. https://doi.org/10.1111/j.1398-9995.2011.02728.x.

45. Ait-Khaled N., Enarson D.A., Chiang C.Y. et al. Management of asthma: a guide to the essentials of good clinical practice. Paris: International Union Against Tuberculosis and Lung Disease; 2008.

46. Papadopoulos N.G., Arakawa H., Carlsen K.H. et al. International consensus on (ICON) pediatric asthma. Allergy. 2012; 67 (8): 976- 977. https://doi.org/10.1111/j.1398-9995.2012.02865.x.

47. Namazova-Baranova L.S., Baranov A.A., Haitov R.M., eds. [Allergology and Immunology]. Moscow: Pediatr; 2020 (in Russian).

48. Doherty G., Bush A. Diagnosing respiratory problems in young children. Practitioner. 2007; 251 (1697): 20, 22-25.

49. Gibson P.G., Powell H., Coughlan J. et al. Self-management education and regular practitioner review for adults with asthma. Cochrane Database Syst. Rev. 2003: (1): CD001117. https://doi.org/10.1002/14651858.CD001117.

50. Fishwick D., D’Souza W., Beasley R. The asthma self-management plan system of care: What does it mean, how is it done, does it work, what models are available, what do patients want and who needs it? Patient Educ. Couns. 1997; 32 (Suppl. 1): S21-33. https://doi.org/10.1016/s0738-3991(97)00093-1.

51. Ramnath V.R., Clark S., Camargo C.A. Jr. Multicenter study of clinical features of sudden-onset versus slower-onset asthma exacerbations requiring hospitalization. Respir. Care. 2007; 52 (8): 1013-1020. Available at: http://rc.rcjournal.com/content/52/8/1013

52. Geelhoed G.C., Landau L.I., Le Souef P.N. Evaluation of SaO2 as a predictor of outcome in 280 children presenting with acute asthma. Ann. Emerg. Med. 1994; 23 (6): 1236-1241. https://doi.org/10.1016/s0196-0644(94)70347-7.

53. Atta J.A., Nunes M.P.T., Fonseca-Guedes C.H.F. et al. Patient and physician evaluation of the severity of acute asthma exacerbations. Braz. J. Med. Biol. Res. 2004; 37 (9): 1321-1330. https://doi.org/10.1590/s0100-879x2004000900006.

54. Nowak R.M., Tomlanovich M.C., Sarkar D.D. et al. Arterial blood gases and pulmonary function testing in acute bronchial asthma. Predicting patient outcomes. JAMA. 1983; 249 (15): 2043-2046. https://doi.org/10.1001/jama.1983.03330390047030.

55. White C.S., Cole R.P., Lubetsky H.W., Austin J.H. Acute asthma: Admission chest radiography in hospitalized adult patients. Chest. 1991; 100 (1): 14-16. https://doi.org/10.1378/chest.100.1.14.

56. Taylor D.R., Bateman E.D., Boulet L.P. et al. A new perspective on concepts of asthma severity and control. Eur. Respir. J. 2008; 32 (3): 545-554. https://doi.org/10.1183/09031936.00155307.

57. O’Byrne P.M., FitzGerald M., Bateman E.D. et al. Inhaled combined budesonide-formoterol as needed in mild asthma. N. Engl. J. Med. 2018; 378 (20): 1865-1876. https://doi.org/10.1056/NEJMoa1715274.

58. Bateman E.D., Reddel H.K., O’Byrne P.M. et al. As-needed budesonide-formoterol versus maintenance budesonide in mild asthma. N. Engl. J. Med. 2018; 378 (20): 1877-1887. https://doi.org/10.1056/NEJMoa1715275.

59. Papi A., Canonica G.W., Maestrelli P. et al. Rescue use of beclomethasone and albuterol in a single inhaler for mild asthma. N. Engl. J. Med. 2007; 356 (20): 2040-2052. https://doi.org/10.1056/NEJMoa063861.

60. Avdeev S.N., Aisanov Z.R., Arhipov V.V. et al. [The principles of the treatment of mild asthma: Consistent guidelines of the Russian Association of Allergology and Clinical Immunology and the Russian Respiratory Society. Prakticheskaya pul’monologiya. 2017; (1): 44-54. Available at: https://atmosphere-ph.ru/modules/Magazines/articles/pulmo/pp_1_2017_82.pdf (in Russian).

61. Pauwels R.A., Pedersen S., Busse W.W. et al. Early intervention with budesonide in mild persistent asthma: a randomised, double-blind trial. Lancet. 2003; 361 (9363): 1071-1076. https://doi.org/10.1016/S0140-6736(03)12891-7.

62. O’Byrne P.M., Barnes P.J., Rodriguez-Roisin R. et al. Low dose inhaled budesonide and formoterol in mild persistent asthma: the OPTIMA randomized trial. Am. J. Respir. Crit. Care Med. 2001; 164 (8, Pt 1): 1392-1397. https://doi.org/10.1164/ajrccm.164.8.2104102.

63. Adams N.P., Bestall J.B., Malouf R. et al. Inhaled beclomethasone versus placebo for chronic asthma. Cochrane Database Syst. Rev. 2005 (1): CD002738. https://doi.org/10.1002/14651858.CD002738.pub2.

64. Wilson A.M., Dempsey O.J., Sims E.J., Lipworth B.J. A comparison of topical budesonide and oral montelukast in seasonal allergic rhinitis and asthma. Clin. Exp. Allergy. 2001; 31 (4): 616-624. https://doi.org/10.1046/j.1365-2222.2001.01088.x.

65. Philip G., Nayak A.S., Berger W.E. et al. The effect of montelukast on rhinitis symptoms in patients with asthma and seasonal allergic rhinitis. Curr. Med. Res. Opin. 2004; 20 (10): 1549-1558. https://doi.org/10.1185/030079904x3348.

66. Guevara J.P., Ducharme F.M., Keren R. et al. Inhaled corticosteroids versus sodium cromoglycate in children and adults with asthma. Cochrane Database Syst. Rev. 2006; 2006 (2): CD003558. https://doi.org/10.1002/14651858.CD003558.pub2.

67. Bisgaard H., Zielen S., Garcia-Garcia M.L. et al. Montelukast reduces asthma exacerbations in 2- to 5-year-old children with intermittent asthma. Am. J. Respir. Crit. Care Med. 2005; 171 (4): 315-322. https://doi.org/10.1164/rccm.200407-894OC.

68. Matsuse H., Tsuchida T., Fukahori S. et al. Retrospective cohort study of leukotriene receptor antagonist therapy for preventing upper respiratory infection-induced acute asthma exacerbations. Allergy Rhinol. (Providence). 2013; 4 (3): e127-131. https://doi.org/10.2500/ar.2013.4.0062.

69. Ducharme F.M., Ni Chroinin M., Greenstone I., Lasserson T.J. Addition of long-acting beta2-agonists to inhaled corticosteroids versus same dose inhaled corticosteroids for chronic asthma in adults and children. Cochrane Database Syst. Rev. 2010; (5): CD005535. https://doi.org/10.1002/14651858.CD005535.pub2.

70. Woodcock A., Vestbo J., Bakerly N.D., et al. Effectiveness of fluticasone furoate plus vilanterol on asthma control in clinical practice: an open-label, parallel group, randomised controlled trial. Lancet. 2017; 390 (10109): 2247-2255. https://doi.org/10.1016/S0140-6736(17)32397-8.

71. Cates C.J., Karner C. Combination formoterol and budesonide as maintenance and reliever therapy versus current best practice (including inhaled steroid maintenance), for chronic asthma in adults and children. Cochrane Database Syst. Rev. 2013; (4): CD007313 https://doi.org/10.1002/14651858.CD007313.pub3.

72. Papi A., Corradi M., Pigeon-Francisco C. et al. Beclometasone- formoterol as maintenance and reliever treatment in patients with asthma: a double-blind, randomised controlled trial. Lancet Respir. Med. 2013; 1 (1): 23-31. https://doi.org/10.1016/S2213-2600(13)70012-2.

73. Patel M., Pilcher J., Pritchard A. et al. Efficacy and safety of maintenance and reliever combination budesonide/formoterol inhaler in patients with asthma at risk of severe exacerbations: a randomised controlled trial. Lancet Respir. Med. 2013; 1 (1): 32-42. https://doi.org/10.1016/S2213-2600(13)70007-9.

74. Bateman E.D., Harrison T.W., Quirce S. et al. Overall asthma control achieved with budesonide/formoterol maintenance and reliever therapy for patients on different treatment steps. Respir. Res. 2011; 12 (1): 38. https://doi.org/10.1186/1465-9921-12-38.

75. Ni Chroinin M., Lasserson T.J., Greenstone I., Ducharme F.M. Addition of long-acting beta-agonists to inhaled corticosteroids for chronic asthma in children. Cochrane Database Syst. Rev. 2009; 8 (3): CD007949. https://doi.org/10.1002/14651858.CD007949.

76. Vaessen-Verberne A.A., van den Berg N.J., van Nierop J.C. et al. Combination therapy salmeterol/fluticasone versus doubling dose of fluticasone in children with asthma. Am. J. Respir. Crit. Care Med. 2010; 182 (10): 1221-1227. https://doi.org/10.1164/rccm.201002-0193OC.

77. Peters S.P., Kunselman S.J., Icitovic N. et al. Tiotropium bromide step-up therapy for adults with uncontrolled asthma. N. Engl. J. Med. 2010; 363 (18): 1715-1726. https://doi.org/10.1056/NEJMoa1008770.

78. Bateman E.D., Kornmann O., Schmidt P. et al. Tiotropium is noninferior to salmeterol in maintaining improved lung function in B16- Arg/Arg patients with asthma. J. Allergy Clin. Immunol. 2011; 128 (2): 315-322. https://doi.org/10.1016/j.jaci.2011.06.004.

79. Kerstjens H.A., Casale T.B., Bleeker E.R. et al. Tiotropium or salmeterol as add-on therapy to inhaled corticosteroids for patients with moderate symptomatic asthma: two replicate, double-blind, placebo-controlled, parallel-group, active-comparator, randomised trials. Lancet Respir. Med. 2015; 3 (5): 367-376. https://doi.org/10.1016/S2213-2600(15)00031-4.

80. Kew K.M., Dahri K. Long-acting muscarinic antagonists (LAMA) added to combination long-acting beta2-agonists and inhaled corticosteroids (LABA/ICS) versus LABA/ICS for adults with asthma. Cochrane Database Syst. Rev. 2016; (1): CD011721. https://doi.org/10.1002/14651858.CD011721.pub2.

81. Rodrigo G.J., Neffen H. Efficacy and safety of tiotropium in schoolage children with moderate-to-severe symptomatic asthma: a systematic review. Pediatr. Allergy Immunol. 2017; 28 (6): 573-578. https://doi.org/10.1111/pai.12759.

82. Rodrigo G.J., Castro-Rodriguez J.A. What is the role of tiotropium in asthma? A systematic review with meta-analysis. Chest. 2015; 147 (2): 388-396. https://doi.org/10.1378/chest.14-1698.

83. Kerstjens H.A., Disse B., Schröder-Babo W. et al. Tiotropium improves lung function in patients with severe uncontrolled asthma: a randomized controlled trial. J. Allergy Clin. Immunol. 2011; 128 (2): 308-314. https://doi.org/10.1016/j.jaci.2011.04.039.

84. Kerstjens H.A., Engel M., Dahl R. et al. Tiotropium in asthma poorly controlled with standard combination therapy. N. Engl. J. Med. 2012; 367 (13): 1198-1207. https://doi.org/10.1056/NEJMoa1208606.

85. FitzGerald M., Moroni-Zentgraf P., Engel M. et al. Once-daily tiotropium Respimat® add-on therapy improves symptom control across severtiies of symptomatic asthma, independent of allergic status. Poster 64426 presented at the American Thoracic Society 2015 International Conference. Denver, USA; 2015.

86. Lee L.A., Bailes Z., Barnes N. et al. Efficacy and safety of once-daily single-inhaler triple therapy (FF/UMEC/VI) versus FF/VI in patients with inadequately controlled asthma (CAPTAIN): a double-blind, randomised, phase 3A trial. Lancet Respir. Med. 2021; 9 (1): 69-84. https://doi.org/10.1016/S2213-2600(20)30389-1.

87. O’Byrne P.M., Naya I.P., Kallen A. et al. Increasing doses of inhaled corticosteroids compared to adding long-acting inhaled beta2-agonists in achieving asthma control. Chest. 2008; 134 (6): 1192-1199. https://doi.org/10.1378/chest.08-1018.

88. Lee L.A., Bailes Z., Barnes N. et al. Efficacy and safety of once-daily single-inhaler triple therapy (FF/UMEC/VI) versus FF/VI in patients with inadequately controlled asthma (CAPTAIN): a double-blind, randomised, phase 3A trial. Lancet Respir. Med. 2021; 9 (1): 69-84. https://doi.org/10.1016/S2213-2600(20)30389-1.

89. Price D.B., Hernandez D., Magyar P. et al. Randomised controlled trial of montelukast plus inhaled budesonide versus double dose inhaled budesonide in adult patients with asthma. Thorax. 2003; 58 (3): 211-216. https://doi.org/10.1136/thorax.58.3.211.

90. Vaquerizo M.J., Casan P., Castillo J. et al. Effect of montelukast added to inhaled budesonide on control of mild to moderate asthma. Thorax. 2003; 58 (3): 204-210. https://doi.org/10.1136/thorax.58.3.204.

91. Tamaoki J., Kondo M., Sakai N. et al. Leukotriene antagonist prevents exacerbation of asthma during reduction of high-dose inhaled corticosteroid. The Tokyo Joshi-Idai Asthma Research Group. Am. J. Respir. Crit. Care Med. 1997; 155 (4): 1235-1240. https://doi.org/10.1164/ajrccm.155.4.9105060.

92. Rodrigo G.J., Neffen H., Castro-Rodriguez J.A. Efficacy and safety of subcutaneous omalizumab vs placebo as addon therapy to corticosteroids for children and adults with asthma: a systematic review. Chest. 2011; 139 (1): 28-35. https://doi.org/10.1378/chest.10-1194.

93. Normansell R., Walker S., Milan S.J. et al. Omalizumab for asthma in adults and children. Cochrane Database Syst. Rev. 2014; (1): CD003559. https://doi.org/10.1002/14651858.CD003559.pub4.

94. Castro M., Zangrilli J., Wechsler M.E. et al. Reslizumab for inadequately controlled asthma with elevated blood eosinophil counts: results from multicenter, parallel, double-blind, randomized, placebo-controlled, phase 3 trials. Lancet Respir. Med. 2015; 3 (5): 355-366. https://doi.org/10.1016/S2213-2600(15)00042-9.

95. Pavord I.D., Korn S., Howarth P. et al. Mepolizumab for severe eosinophilic asthma (DREAM): a multicentre, double-blind, placebo-controlled trial. Lancet. 2012; 380 (9842): 651-659. https://doi.org/10.1016/S0140-6736(12)60988-X.

96. Ortega H.G., Liu M.C., Pavord I.D. et al. Mepolizumab treatment in patients with severe eosinophilic asthma. N. Engl. J. Med. 2014; 371 (13): 1198-1207. https://doi.org/10.1056/NEJMoa1403290.

97. Bel E.H., Wenzel S.E., Thompson P.J. et al. Oral glucocorticoid-sparing effect of mepolizumab in eosinophilic asthma. N. Engl. J. Med. 2014; 371 (13): 1189-1197. https://doi.org/10.1056/NEJMoa1403291.

98. FitzGerald J.M., Bleecker E.R., Nair P. et al. Benralizumab, an anti-interleukin-5 receptor α monoclonal antibody, as add-on treatment for patients with severe, uncontrolled, eosinophilic asthma (CALIMA): a randomized, double-blind, placebo-controlled phase 3 trial. Lancet. 2016; 388 (10056): 2128-2141. https://doi.org/10.1016/S0140-6736(16)31322-8.

99. Bleecker E.R, FitzGerald J.M., Chanez P. et al. Efficacy and safety of benralizumab for patients with severe asthma uncontrolled with high-dosage inhaled corticosteroids and long-acting β2 -agonists (SIROCCO): a randomized, multicentre, placebo-controlled phase 3 trial. Lancet. 2016; 388 (10056): 2115-2127. https://doi.org/10.1016/S0140-6736(16)31324-1.

100. Castro M., Corren J., Pavord I.D. et al. Dupilumab efficacy and safety in moderate-to-severe uncontrolled asthma. N. Engl. J. Med. 2018; 378 (26): 2486-2496. https://doi.org/10.1056/NEJMoa1804092.

101. Rabe K.F., Nair P., Brusselle G. et al. Efficacy and safety of dupilumab in glucocorticoid-dependent severe asthma. N. Engl. J. Med. 2018; 378 (26): 2475-2485. https://doi.org/10.1056/NEJMoa1804093.

102. Zayed Y., Kheiri B., Banifadel M. et al. Dupilumab safety and efficacy in uncontrolled asthma: a systematic review and meta-analysis of randomized clinical trials. J. Asthma. 2018; 56 (10): 1110-1119. https://doi.org/10.1080/02770903.2018.1520865.

103. Global Initiative for Asthma. Difficult-to-treat and severe asthma in adolescent and adult patients: diagnosis and management. A GINA Pocket Guide for Health Professionals. 2019. Available at: www.ginasthma.org

104. Chung K.F., Wenzel S.E., Brozek J.L. et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur. Respir. J. 2014; 43 (2): 343-373. https://doi.org/10.1183/09031936.00202013.

105. Rivington R.N., Boulet L.P., Côté J. et al. Efficacy of Uniphyl, salbutamol, and their combination in asthmatic patients on highdose inhaled steroids. Am. J. Respir. Crit. Care Med. 1995; 151 (2, Pt 1): 325-332. https://doi.org/10.1164/ajrccm.151.2.7842186.

106. Vogelberg C., Moroni-Zentgraf P., Lronaviciute-Klimantaviciene M. et al. A randomized dose-ranging study of tiotropium Respimat in children with symptomatic asthma despite inhaled corticosteroids. Repir. Res. 2015; 16 (1): 20. https://doi.org/10.1186/s12931-015-0175-9.

107. Guo J.J., Tsai K., Kelton C.M.L. et al. Risk of serious asthma exacerbations associated with long-acting beta agonists among patients with asthma: a retrospective cohort study. Ann. Allergy Asthma Immunol. 2011; 106 (3): 214-222. https://doi.org/10.1016/j.anai.2010.12.008.

108. Melani A.S., Bonavia M., Cilenti V. et al. Inhaler mishandling remains common in real life and is associated with reduced disease control. Respir. Med. 2011; 105 (6): 930-938. https://doi.org/10.1016/j.rmed.2011.01.005.

109. Fink J.B., Rubin B.K. Problems with inhaler use: a call for improved clinician and patient education. Respir. Care. 2005; 50 (10): 1360-1375. Available at: http://rc.rcjournal.com/content/50/10/1360

110. Basheti I.A., Reddel H.K., Armour C.L., Bosnic-Anticevich S.Z. Improved asthma outcomes with a simple inhaler technique intervention by community pharmacists. J. Allergy Clin. Immunol. 2007; 119 (6): 1537-1538. https://doi.org/10.1016/j.jaci.2007.02.037.

111. Honkoop P.J., Loymans R.J.B., Termeer E.H. et al. Asthma control cost-utility randomized trial evaluation (ACCURATE): the goals of asthma treatment. BMC Pulm. Med. 2011; 11: 53. https://doi.org/10.1186/1471-2466-11-53.

112. Eber E., Midulla F., eds. Paediatric Respiratory Medicine. ERS Handbook. 1st edn. Charlesworth Press; 2013. Available at: https://dl.uswr.ac.ir/bitstream/Hannan/140448/1/9781849840385.pdf

113. Abramson M.J., Puy R.M., Weiner J.M. Injection allergen immunotherapy for asthma. Cochrane Database Syst. Rev. 2010; (8): CD001186. https://doi.org/10.1002/14651858.CD001186.pub2.

114. Tao L., Shi B., Shi G., Wan H. Efficacy of sublingual immunotherapy for allergic asthma: retrospective meta-analysis of randomized, double-blind and placebo-controlled trials. Clin. Respir. J. 2014; 8 (2): 192-205. https://doi.org/10.1111/crj.12058.

115. Virchow J.C., Backer V., Kuna P. et al. Efficacy of a house dust mite sublingual allergen immunotherapy tablet in adults with allergic asthma: a randomized clinical trial. JAMA. 2016; 315 (16): 1715-1725. https://doi.org/10.1001/jama.2016.3964.

116. Mosbech H., Deckelmann R., de Blay F. et al. Standardized quality (SQ) house dust mite sublingual immunotherapy tablet (ALK) reduces inhaled corticosteroid use while maintaining asthma control: a randomized, double-blind, placebo-controlled trial. J. Allergy Clin. Immunol. 2014; 134 (3): 568-575.e7. https://doi.org/10.1016/j.jaci.2014.03.019.

117. Hondras M.A., Linde K., Jones A.P. Manual therapy for asthma. Cochrane Database Syst. Rev. 2005; (2): CD001002. https://doi.org/10.1002/14651858.CD001002.pub2.

118. Cooper S., Oborne J., Newton S. et al. Effect of two breathing exercises (Buteyko and pranayama) in asthma: a randomized controlled trial. Thorax. 2003; 58 (8): 674-679. https://doi.org/10.1136/thorax.58.8.674.

119. Avdeev S.N., Aisanov Z.R., Belevskiy A.S. et al. [A strategy for improvement in diagnosis and treatment of bronchial asthma in primary care. Pul’monologiya. 2019; 29 (4): 457-467. https://doi.org/10.18093/0869-0189-2019-29-4-457-467 (in Russian).

120. Perrin K., Wijesinghe M., Healy B., et al. Randomised controlled trial of high concentration versus titrated oxygen therapy in severe exacerbations of asthma. Thorax. 2011; 66 (11): 937-941. https://doi.org/10.1136/thx.2010.155259.

121. Edmonds M.L., Milan S.J., Camargo C.A. et al. Early use of inhaled corticosteroids in the emergency department treatment of acute asthma. Cochrane Database Syst. Rev. 2012; (12): CD002308. https://doi.org/10.1002/14651858.CD002308.pub2.

122. Cates C.J., Welsh E.J., Rowe B.H. Holding chambers (spacers) versus nebulisers for beta-agonist treatment of acute asthma. Cochrane Database Syst. Rev. 2013; (9): CD000052. https://doi.org/10.1002/14651858.CD000052.pub3.

123. Rodrigo G.J., Rodrigo C., Hall J.B. Acute asthma in adults: a review. Chest. 2004; 125 (3): 1081-1102. https://doi.org/10.1378/chest.125.3.1081.

124. Hasegawa T., Ishihara K., Takakura S. et al. Duration of systemic corticosteroids in the treatment of asthma exacerbation; a randomized study. Intern. Med. 2000; 39 (10): 794-797. https://doi.org/10.2169/internalmedicine.39.794.

125. Jones A.M., Munavvar M., Vail A. et al. Prospective, placebo-controlled trial of 5 vs 10 days of oral prednisolone in acute adult asthma. Respir. Med. 2002; 96 (11): 950-954. https://doi.org/10.1053/rmed.2002.1369.

126. Avdeev S.N., Zhestkov A.V., Leshhenko I.V. et al. [Nebulized budesonide in acute severe asthma: comparison with systemic corticosteroids. Multicenre randomized controlled trial. Pul’monologiya. 2006; (4): 58-67. Available at: https://journal.pulmonology.ru/pulm/article/view/1476 (in Russian).

127. Ovcharenko S.I., Peredel”skaya O.A., Morozova N.V., Makolkin V.I. [Nebulized bronchodilators and pulmicort in therapy of severe exacerbation of bronchial asthma. Pul’monologiya. 2003; (6): 75-83. Available at: https://journal.pulmonology.ru/pulm/article/view/2597/2029 (in Russian).

128. Ediger D., Coşkun F., Kunt Uzaskan E. et al. Clinical effectiveness of nebulized budesonide in the treatment of acute asthma attacks. Tuberkuloz ve Toraks Dergisi. 2006; 54 (2): 128-136. Available at: http://www.tuberktoraks.org/managete/fu_folder/2006-02/2006-54-2-128-136.pdf

129. Higenbottam T., Britton J., Lawrence D. et al. Comparison of nebulised Budesonide and Prednisolone in severe asthma exacerbation in adults. BioDrugs. 2000; 14 (4): 247-254. https://doi.org/10.2165/00063030-200014040-00004.

130. Chien J.W., Ciufo R., Novak R. et al. Uncontrolled oxygen administration and respiratory failure in acute asthma. Chest. 2000; 117 (3): 728-733. https://doi.org/10.1378/chest.117.3.728.

131. Rodrigo G.J., Rodriquez Verde M., Peregalli V., Rodrigo C. Effects of short-term 28% and 100% oxygen on PaCO2 and peak expiratory flow rate in acute asthma: a randomized trial. Chest. 2003; 124 (4): 1312-1317. https://doi.org/10.1378/chest.124.4.1312.

132. Rodrigo G.J., Castro-Rodriguez J.A. Anticholinergics in the treatment of children and adults with acute asthma: a systematic review with meta-analysis. Thorax. 2005; 60 (9): 740-746. https://doi.org/10.1136/thx.2005.040444.

133. Camargo C.A. Jr, Spooner C.H., Rowe B.H. Continuous versus intermittent beta-agonists in the treatment of acute asthma. Cochrane Database Syst. Rev. 2003; (4): CD001115. https://doi.org/10.1002/14651858.CD001115.

134. Nair P., Milan S.J., Rowe B.H. Addition of intravenous aminophylline to inhaled beta(2)-agonists in adults with acute asthma. Cochrane Database Syst. Rev. 2012; (12): CD002742. https://doi.org/10.1002/14651858.CD002742.pub2.

135. Ayres J.G. Classification and management of brittle asthma. Br. J. Hosp. Med. 1997; 57 (8): 387-389.

136. Kolbe J., Fergusson W., Garrett J. Rapid onset asthma: a severe but uncommon manifestation. Thorax. 1998; 53 (4): 241-247. https://doi.org/10.1136/thx.53.4.241.

137. Rowe B.H., Bretzlaff J.A., Bourdon C. et al. Magnesium sulfate for treating exacerbations of acute asthma in the emergency department. Cochrane Database Syst. Rev. 2000; (2): CD001490. https://doi.org/10.1002/14651858.CD001490.

138. FitzGerald J.M. Magnesium sulfate is effective for severe acute asthma treated in the emergency department. West J. Med. 2000; 172 (2): 96. https://doi.org/10.1136/ewjm.172.2.96-a.

139. Gallegos-Solorzano M.C., Perez-Padilla R., Hernandez-Zenteno R.J. Usefulness of inhaled magnesium sulfate in the coadjuvant management of severe asthma crisis in an emergency department. Pulm. Pharmacol. Ther. 2010; 23 (5): 432-437. https://doi.org/10.1016/j.pupt.2010.04.006.

140. Rodrigo G.J., Castro-Rodriguez J.A. Heliox-driven beta2-agonists nebulization for children and adults with acute asthma: a systematic review with meta-analysis. Ann. Allergy Asthma Immunol. 2014; 112 (1): 29-34. https://doi.org/10.1016/j.anai.2013.09.024.

141. Pozin N., Montesantos S., Katz I. et al. Calculated ventilation and effort distribution as a measure of respiratory disease and Heliox effectiveness. J. Biomech. 2017; 60: 100-109. https://doi.org/10.1016/j.jbiomech.2017.06.009.

142. Silverman R.A., Nowak R.M., Korenblat P.E. et al. Zafirlukast treatment for acute asthma: evaluation in a randomized, doubleblind, multicenter trial. Chest. 2004; 126 (5): 1480-1489. https://doi.org/10.1378/chest.126.5.1480.

143. Ramsay C.F., Pearson D., Mildenhall S., Wilson A.M. Oral montelukast in acute asthma exacerbations: a randomised, doubleblind, placebo-controlled trial. Thorax. 2011; 66 (1): 7-11. https://doi.org/10.1136/thx.2010.135038.

144. Gupta D., Hath A., Agarwal R., Behera D. A prospective randomized controlled trial on the efficacy of noninvasive ventilation in severe acute asthma. Respir. Care. 2010; 55 (5): 536-543. Available at: http://rc.rcjournal.com/content/55/5/536

145. Georgopoulos D., Burchardi H. Ventilation strategies in adult patients with status asthmaticus. Eur. Respir. Mon. 1998; 3: 45-83.

146. Avdeev S.N. [Respiratory support for status asthmaticus]. Chuchalin A.G., ed. [Bronchial Asthma in Adults: Clinical guidelines]. Moscow: Atmosfera; 2002: 130-155 (in Russian).

147. Kuyper L.M., Pare P.D., Hogg J.C. et al. Characterization of airway plugging in fatal asthma. Am. J. Med. 2003; 115 (1): 6-11. https://doi.org/10.1016/s0002-9343(03)00241-9.

148. National library of Medicine. Expert panel report 3: Guidelines for the diagnosis and management of asthma: Clinical practice guidelines. 2007. Available at: https://www.ncbi.nlm.nih.gov/books/NBK7232

149. Grunfeld A., FitzGerald J. Discharge considerations for adult asthmatic patients treated in emergency departments. Can. Respir. J. 1996; 3 (5): 322-327. https://doi.org/10.1155/1996/254627.

150. Edmonds M.L., Milan S.J., Brenner B.E. et al. Inhaled steroids for acute asthma following emergency department discharge. Cochrane Database Syst. Rev. 2012; (12): CD002316. https://doi.org/10.1002/14651858.CD002316.pub2.

151. Rowe B.H., Bota G.W., Fabris L. et al. Inhaled budesonide in addition to oral steroids to prevent asthma relapse following discharge from the emergency department: a randomized controlled trial. JAMA. 1999; 281 (22): 2219-2226. https://doi.org/10.1001/jama.281.22.2119.

152. Schatz M., Rachelefsky G., Krishnan J.A. Follow-up after acute asthma episodes: what improves future outcomes? Proc. Am. Thorac. Soc. 2009; 6 (4): 386-393. https://doi.org/10.1513/pats.p09st6.

153. Jaffuel D., Fabry-Vendrand C., Darnal E. et al. Perception of oral corticosteroids in adult patients with asthma in France. J. Asthma. 2021; 58 (7): 946-957. https://doi.org/10.1080/02770903.2020.1748048.

154. Beckhaus A.A., Riutort M.C., Castro-Rodriguez J.A. Inhaled versus systemic corticosteroids for acute asthma in children: a systematic review. Pediatr. Pulmonol. 2014; 49 (4): 326-334. https://doi.org/10.1002/ppul.22846.

155. Wilson N.M., Silverman M. Treatment of acute, episodic asthma in preschool children using intermittent high dose inhaled steroids at home. Arch. Dis. Child. 1990; 65 (4): 407-410. https://doi.org/10.1136/adc.65.4.407.

156. Su X.M., Yu N., Kong L.F., Kang J. Effectiveness of inhaled corticosteroids in the treatment of acute asthma in children in the emergency department: a meta-analysis. Ann. Med. 2014; 46 (1): 24-30. https://doi.org/10.3109/07853890.2013.859855.

157. Rohrer V., Schmidt-Trucksäss A. [Impact of exercise, sport and rehabilitation therapy in asthma and COPD]. Ther. Umsch. 2014; 71 (5): 295-300. https://doi.org/10.1024/0040-5930/a000516 (in German).

158. Hennenberger P.K., Liang X., Lilienberg L. et al. Occupational exposures associated with severe exacerbation of asthma. Int. J. Tuberc. Lung. Dis. 2015; 19 (2): 244-250. https://doi.org/10.5588/ijtld.14.0132.

159. Oland A.A., Booster G.D., Bender B.G. Psychological and lifestyle risk factors for asthma exacerbations and morbidity in children. World Allergy Organ. J. 2017; 10 (1): 35. https://doi.org/10.1186/s40413-017-0169-9.

160. Aarniala B.S., Poussa T., Kvarnström J. et al. Immediate and long term effects of weight reduction in obese people with asthma: randomised controlled study. BMJ. 2000; 320 (7238): 827-832. https://doi.org/10.1136/bmj.320.7238.827.

161. Hasegawa K., Tsugawa Y., Lopez B.L. et al. Body mass index and risk of hospitalization among adults presenting with asthma exacerbation to the emergency department. Ann. Am. Thorac. Soc. 2014; 11 (9): 1439-1444. https://doi.org/10.1513/AnnalsATS.201406-270BC.

162. Gamble J., Stevenson M., Heaney L.G. A study of a multi-level intervention to improve non-adherence in difficult to control asthma. Respir. Med. 2011; 105 (9): 1308-1315. https://doi.org/10.1016/j.rmed.2011.03.019.

163. Wenzel S. Severe asthma in adults. Am. J. Respir. Crit. Care Med. 2005; 172 (2): 149-160. https://doi.org/10.1164/rccm.200409-1181PP.

164. Petsky H.L., Cates C.J., Lasserson T.J. et al. A systematic review and meta-analysis: tailoring asthma treatment on eosinophilic markers (exhaled nitric oxide or sputum eosinophils). Thorax. 2012; 67 (3): 199-208. https://doi.org/10.1136/thx.2010.135574.

165. Wang Y., Wang C.Z., Lin K.X. et al. Comparison of inhaled corticosteroid combined with theophylline and double-dose inhaled corticosteroid in moderate to severe asthma. Respirology. 2005; 10 (2): 189-195. https://doi.org/10.1111/j.1440-1843.2005.00697.x.

166. Murphy V.E., Gibson P.G. Asthma in pregnancy. Clin. Chest Med. 2011; 32 (1): 93-110. https://doi.org/10.1016/j.ccm.2010.10.001.

167. Dombrowski M.P., Schatz M., Wise R. et al. Asthma during pregnancy. Obstet. Gynecol. 2004; 103 (1): 5-12. https://doi.org/10.1097/01.AOG.0000103994.75162.

168. 168. Zacharasiewicz A. Maternal smoking in pregnancy and its influence on childhood asthma. ERJ Open Res. 2016; 2 (3): 00042-2016. https://doi.org/10.1183/23120541.00042-2016.

169. Eltonsy S., Forget A., Blais L. Beta2-agonists use during pregnancy and the risk of congenital malformations. Birth. Defects Res. A Clin. Mol. Teratol. 2011; 91 (11): 937-947. https://doi.org/10.1002/bdra.22850.

170. Schatz M. Asthma treatment during pregnancy. What can be safely taken? Drug Saf. 1997; 16 (5): 342-350. https://doi.org/10.2165/00002018-199716050-00005.

171. Lim A., Stewart K., König K., George J. Systematic review of the safety of regular preventive asthma medications during pregnancy. Ann. Pharmacother. 2011; 45 (7-8): 931-945. https://doi.org/10.1345/aph.1P764.

172. NAEPP Expert Panel Report. Managing asthma during pregnancy: recommendations for pharmacologic treatment - 2004 update. J. Allergy Clin. Immunol. 2005; 115 (1): 34-46. https://doi.org/10.1016/j.jaci.2004.10.023.

173. Wendel P.J., Ramin S.M., Barnett-Hamm C. et al. Asthma treatment in pregnancy: a randomized controlled study. Am. J. Obstet Gynecol. 1996; 175 (1): 150-154. https://doi.org/10.1016/s0002-9378(96)70265-x.

174. Giles W., Murphy V. Asthma in pregnancy: a review. Obstet. Med. 2013; 6 (2): 58-63. https://doi.org/10.1258/OM.2012.120008.

175. Michaud P.A., Suris J.C., Viner R. The adolescent with a chronic condition: epidemiology, developmental issues and health care provision. Geneva: World Health Organization; 2007. Available at: https://apps.who.int/iris/handle/10665/43775?locale-attribute=ru&-mode=full

176. Baur X., Sigsgaard T., Aasen T.B. et al. Guidelines for the management of work-related asthma. Eur. Respir. J. 2012; 39 (3): 529-545. https://doi.org/10.1183/09031936.00096111.

177. Henneberger P.K., Patel J.R., de Groene G.J. et al. The effectiveness of removal from exposure and reduction of exposure for managing occupational asthma: summary of an updated Cochrane systematic review. Am. J. Ind. Med. 2020; 64 (3): 165-169. https://doi.org/10.1002/ajim.23208.

178. Papadopoulos N.G., Arakawa H., Carlsen K.H. et al. International consensus on (ICON) pediatric asthma. Allergy. 2012; 67 (8): 976-997. https://doi.org/10.1111/j.1398-9995.2012.02865.x.

179. Allergology and Immunology: clinical guidelines for pediatricians. 3rd edn. Moscow: The Union of Pediatricians of Russia; 2011 (in Russian).

180. Zeiger R.S., Schatz M., Zhang F. et al. Elevated exhaled nitric oxide is a clinical indicator of future uncontrolled asthma in asthmatic patients on inhaled corticosteroids. J. Allergy Clin. Immunol. 2011; 128 (2): 412-414. https://doi.org/10.1016/j.jaci.2011.06.008.

181. Schatz M., Sorkness C.A., Li J.T. et al. Asthma Control Test: reliability, validity, and responsiveness in patients not previously followed by asthma specialists. J. Allergy Clin. Immunol. 2006; 117 (3): 549-556. https://doi.org/10.1016/j.jaci.2006.01.011.

182. Schatz M., Mosen D.M., Kosinski M. et al. Validity of the asthma control test completed at home. Am. J. Manag. Care. 2007; 13 (12): 661-667.

183. Liu A.H., Zeiger R., Sorkness C. et al. Development and cross-sectional validation of the childhood asthma control test. J. Allergy Clin. Immunol. 2007; 119 (4): 817-825. https://doi.org/10.1016/j.jaci.2006.12.662.

184. Juniper E.F., O’Byrne P.M., Guyatt G.H. et al. Development and validation of a questionnaire to measure asthma control. Eur. Respir. J. 1999; 14 (4): 902-907. https://doi.org/10.1034/j.1399-3003.1999.14d29.x.


Review

For citations:


Chuchalin A.G., Avdeev S.N., Aisanov Z.R., Belevskiy A.S., Vasil’eva O.S., Geppe N.A., Ignatova G.L., Knyazheskaya N.P., Malakhov A.B., Meshcheryakova N.I., Nenasheva N.M., Fassakhov R.S., Khaitov R.M., Il’ina N.I., Kurbacheva O.M., Astafieva N.G., Demko I.V., Fomina D.S., Namazova-Baranova L.S., Baranov A.A., Vishneva E.A., Novik G.A. Federal guidelines on diagnosis and treatment of bronchial asthma. PULMONOLOGIYA. 2022;32(3):393-447. (In Russ.) https://doi.org/10.18093/0869-0189-2022-32-3-393-447

Views: 9133


ISSN 0869-0189 (Print)
ISSN 2541-9617 (Online)