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    Academic Journal

    Πηγή: Meditsinskiy sovet = Medical Council; № 23 (2024); 80-86 ; Медицинский Совет; № 23 (2024); 80-86 ; 2658-5790 ; 2079-701X

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    Relation: https://www.med-sovet.pro/jour/article/view/8830/7739; Larsen K, Tos M. Clinical course of patients with primary nasal polyps. Acta Otolaryngol. 1994;114(5):556–559. https://doi.org/10.3109/00016489409126104.; Slater A, Smallman LA, Logan AC, Drake-Lee AB. Mucociliary function in patients with nasal polyps. Clin Otolaryngol Allied Sci. 1996;21(4):343–347. https://doi.org/10.1111/j.1365-2273.1996.tb01084.x.; Носуля ЕВ, Ким ИА, Афанасьева НВ, Сумбаева ОВ. Распространенность полипозного риносинусита среди городского населения Восточной Сибири. Российская ринология. 2007;(1):4–8. Режим доступа: https://elibrary.ru/hzqvaz.; Арефьева НА, Вишняков ВВ, Вахрушев СГ. Полипозный риносинусит. Клинические рекомендации. М.; 2010.; Пискунов ГЗ. Клинические фенотипы полипозного риносинусита. Российская ринология. 2019;27(4):224–231. https://doi.org/10.17116/rosrino201927041224.; Reddel HK, Bacharier LB, Bateman ED, Brightling CE, Brusselle GG, Buhl R et al. Global Initiative for Asthma Strategy 2021: executive summary and rationale for key changes. Am J Respir Crit Care Med. 2022;205(1):17–35. https://doi.org/10.1164/rccm.202109-2205PP.; Chuchalin AG, Khaltaev N, Antonov NS, Galkin DV, Manakov LG, Antonini P et al. Chronic respiratory diseases and risk factors in 12 regions of the Russian Federation. Int J Chron Obstruct Pulmon Dis. 2014;9:963–974. https://doi.org/10.2147/copd.s67283.; Геппе НА, Колосова НГ. Национальная программа «Бронхиальная астма у детей», 2012. Стратегия лечения. Consilium Medicum. Пульмонология (Прил.). 2012;(1):39–41. Режим доступа: https://omnidoctor.ru/library/izdaniya-dlya-vrachey/consilium-medicum/cm2012/pulmo_2012_pril/natsionalnaya-programma-bronkhialnaya-astma-u-detey-2012-strategiya-lecheniya.; Samoliński B, Szczesnowicz-Dabrowska P. Relationship between inflammation of upper and lower respiratory airways. Otolaryngol Pol. 2002;56(1):49–55. Available at: https://pubmed.ncbi.nlm.nih.gov/12053668/.; Serrano E, Neukirch F, Pribil C, Jankowski R, Klossek JM, Chanal I, El Hasnaoui A. Nasal polyposis in France: Impact on sleep and quality of life. J Laringol Otol. 2005;119(7):543–549. https://doi.org/10.1258/0022215054352108.; Bauchau V, Durham SR. Prevalence and rate of diagnosis of allergic rhinitis in Europe. Eur Respir J. 2004;24(5):758–764. https://doi.org/10.1183/09031936.04.00013904.; Bachert C, van Cauwenberge P, Olbrecht J, van Schoor J. Prevalence, classification and perception of allergic and nonallergic rhinitis in Belgium. Allergy. 2006;61(6):693–698. https://doi.org/10.1111/j.1398-9995.2006.01054.x.; Nathan RA, O Meltzer E, Derebery J, Campbell UB, Stang PE, Corrao MA et al. The prevalence of nasal symptoms attributed to allergies in the United States: findings from the burden of rhinitis in an America survey. Allergy Asthma Proc. 2008;29(6):600–608. https://doi.org/10.2500/aap.2008.29.3179.; Katelaris CH, Lee BW, Potter PC, Maspero JF, Cingi C, Lopatin A et al. Prevalence and diversity of allergic rhinitis in regions of the world beyond Europe and North America. Clin Exp Allergy. 2012;42(2):186–207. https://doi.org/10.1111/j.1365-2222.2011.03891.x.; Ridolo E, Montagni M, Bonzano L, Incorvaia C, Canonica GW et al. Bilastine: new insight into antihistamine treatment. Clin Mol Allergy. 2015;13(1):1. https://doi.org/10.1186/s12948-015-0008-x.; Cingi C, Yorgancioglu A, Cingi CC, Oguzulgen K, Muluk NB, Ulusoy S et al. The “physician on call patient engagement trial” (POPET): measuring the impact of a mobile patient engagement application on health outcomes and quality of life in allergic rhinitis and asthma patients. Int Forum Allergy Rhinol. 2015;5(6):487–497. https://doi.org/10.1002/alr.21468.; Xiao J, Wu WX, Ye YY, Lin WJ, Wang L. A network meta-analysis of randomized controlled trials focusing on different allergic rhinitis medications. Am J Ther. 2016;23(6):e1568-e1578. https://doi.org/10.1097/mjt.0000000000000242.; Савлевич ЕЛ, Гаганов ЛЕ, Егоров ВИ, Курбачева ОМ, Герасимов АН, Шачнев КН. Сравнительное пилотное исследование эндотипов хронического полипозного риносинусита у пациентов, проживающих в разных географических регионах Российской Федерации. Иммунология. 2018;39(4):208–213. Режим доступа: https://cyberleninka.ru/article/n/sravnitelnoe-pilotnoe-issledovanie-endotipov-hronicheskogo-polipoznogorinosinusita-u-patsientov-prozhivayuschih-v-raznyh/viewer.; Tomassen P, Vandeplas G, Van Zele T, Cardell LO, Arebro J, Olze H et al. Inflammatory endotypes of chronic rhinosinusitis based on cluster analysis of biomarkers. J Allergy Clin Immunol. 2016;137(5):1449–1456.e4. https://doi.org/10.1016/j.jaci.2015.12.1324.; Fokkens WJ, Lund VJ, Hopkins C, Hellings PW, Kern R, Reitsma S et al. European position paper on rhinosinusitis and nasal polyps 2020. Rhinology. 2020;58(Suppl. 29):1–464. https://doi.org/10.4193/rhin20.600.; Lund VJ, Kennedy DW. Quantification for staging sinusitis. Ann Otol Rhinol Laryngol Suppl. 1995;167:17–21. Available at: https://pubmed.ncbi.nlm.nih.gov/7574265/.; Ortega HG, Liu MC, Pavord ID, Brusselle GG, FitzGerald JM, Chetta A 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.; Chipps BE, Newbold P, Hirsch I, Trudo F, Goldman M. Benralizumab efficacy by atopy status and serum immunoglobulin E for patients with severe, uncontrolled asthma. Ann Allergy Asthma Immunol. 2018;120(5):504–511. https://doi.org/10.1016/j.anai.2018.01.030.; Козлов ВС, Савлевич ЕЛ. Полипозный риносинусит. Современные подходы к изучению патогенеза, диагностике и лечению. Вестник оториноларингологии. 2015;80(4):95–99. https://doi.org/10.17116/otorino201580495-99.; Рязанцев СВ, Будковая МА. Тактика лечения полипозного риносинусита. Российская оториноларингология. 2017;(2):162–169. https://doi.org/10.18692/1810-4800-2017-2-162-169.; Лопатин АС. Современные теории патогенеза полипозного риносинусита. Пульмонология. 2003;(5):110–115. Режим доступа: https://journal.pulmonology.ru/pulm/article/view/2629/2061.; Пискунов ГЗ. Физиологическое и патофизиологическое обоснование функциональной риносинусохирургии. Folia Otorhinolaryngologiae et Pathologiae Respiratoriae. 2018;24(1):23–28. Режим доступа: https://www.elibrary.ru/yulkqc.; Курбачева ОМ, Дынева МЕ, Ильина НИ. Дупилумаб: основные аспекты применения при T2-опосредованных заболеваниях. Медицинский cовет. 2021;(16):186–196. https://doi.org/10.21518/2079-701X-2021-16-186-196.; Hopkins C. Ethical dilemmas associated with the introduction of biologic treatments in chronic rhinosinusitis with nasal polyps. Rhinology. 2022;60(3):162–168. https://doi.org/10.4193/Rhin21.477.; Karin J, Tim D, Gabriele H, Cardell LO, Marit W, Claus B. Type 2 inflammatory shift in chronic rhinosinusitis during 2007–2018 in Belgium. Laryngoscope. 2021;131(5):E1408–E1414. https://doi.org/10.1002/lary.29128.; Аллахверанов ДАО, Юнусов АС, Рябинин АГ. Отдаленные результаты эндоскопических методов лечения хронического полипозного риносинусита. Российская оториноларингология. 2015;(3):158–160. Режим доступа: https://cyberleninka.ru/article/n/otdalennye-rezultaty-endoskopicheskihmetodov-lecheniya-hronicheskogo-polipoznogo-rinosinusita.; Завадский АВ, Завадский НВ, Золотарева МА. Ведение послеоперационного периода у больных полипозом носа. Российская оториноларингология. 2015;(5):89–94. Режим доступа: https://www.elibrary.ru/unldtd.; Широкая АВ, Свистушкин ВМ, Шатохина СН, Шабалин ВН. Оценка эффективности лечения больных полипозным риносинуситом и прогноз его течения. Российская оториноларингология. 2013;(2):96–104. Режим доступа: https://cyberleninka.ru/article/n/otsenka-effektivnosti-lecheniyabolnyh-polipoznym-rinosinusitom-i-prognoz-ego-techeniya.; Campbell RG. Risks and management of long-term corticosteroid use in chronic rhinosinusitis. Curr Opin Otolaryngol Head Neck Surg. 2018;26(1):1–7. https://doi.org/10.1097/moo.0000000000000421.; Han J, Gross G, Mannent L, Amin N, Cho S, Bachert C. Dupilumab Improves Sinus Opacification in All Sinuses in Patients With Severe Chronic Rhinosinusitis With Nasal Polyps (CRSwNP): Results From the SINUS-24 Phase 3 Study. J Allergy Clin Immunol. 2020;145(2):AB251. https://doi.org/10.1016/j.jaci.2019.12.109.; Fokkens WJ, Lund V, Bachert C, Mullol J, Bjermer L, Bousquet J et al. EUFOREA consensus on biologics for CRSwNP with or without asthma. Allergy. 2019;74(12):2312–2319. https://doi.org/10.1111/all.13875.; Al-Ahmad M, Alsaleh S, Al-Reefy H, Abduwani JA, Nasr I, Al Abri R et al. Expert opinion on biological treatment of chronic rhinosinusitis with nasal polyps in the gulf region. J Asthma Allergy. 2022;15:1–12. https://doi.org/10.2147/jaa.s321017.

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    Academic Journal

    Πηγή: SCIENTIFIC JOURNAL OF APPLIED AND MEDICAL SCIENCES; Vol. 3 No. 9 (2024): AMALIY VA TIBBIYOT FANLARI ILMIY JURNALI; 28-33 ; НАУЧНЫЙ ЖУРНАЛ ПРИКЛАДНЫХ И МЕДИЦИНСКИХ НАУК; Том 3 № 9 (2024): AMALIY VA TIBBIYOT FANLARI ILMIY JURNALI; 28-33 ; 2181-3469

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  10. 10
    Academic Journal

    Πηγή: Meditsinskiy sovet = Medical Council; № 20 (2024); 24-28 ; Медицинский Совет; № 20 (2024); 24-28 ; 2658-5790 ; 2079-701X

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.med-sovet.pro/jour/article/view/8754/7687; Cunha AS, Raposo B, Dias F, Henriques S, Martinho H, Pedro AR. Management of Chronic Obstructive Pulmonary Disease: Constraints in Patient Pathway and Mitigation Strategies. Port J Public Health. 2024;12:1-8. https://doi.org/10.1159/000535474.; Самородская ИВ, Болотова ЕВ, Дудникова АВ. Динамика и структура смертности от болезней органов дыхания и COVID-19 в Российской Федерации за 2019-2021 гг. Клиническая медицина. 2022;100(11-12):535-539. https://doi.org/10.30629/0023-2149-2022-100-11-12-535-539.; Koopman M, Posthuma R, Vanfleteren LEGW, Simons SO, Franssen FME. Lung Hyperinflation as Treatable Trait in Chronic Obstructive Pulmonary Disease: A Narrative Review. Int J Chron Obstruct Pulmon Dis. 2024;19:1561-1578. https://doi.org/10.2147/COPD.S458324.; Cazzola M, Rogliani P, Laitano R, Calzetta L, Matera MG. Beyond Dual bronchodilation - Triple Therapy, When and Why. Int J Chron Obstruct Pulmon Dis. 2022;17:165-180. https://doi.org/10.2147/COPD.S345263.; Болотова ЕВ, Дудникова АВ, Шульженко ЛВ. Опыт применения тройной фиксированной комбинации в лечении больных хронической обструктивной болезнью легких. Терапевтический архив. 2022;94(3):396-400. https://doi.org/10.26442/00403660.2022.03.201406.; Авдеев СН, Айсанов ЗР, Ардашева ТВ, Белевский АС, Демко ИВ, Зайцев АА и др. Хроническая обструктивная болезнь легких: клинические рекомендации. 2023 г. Режим доступа: https://spulmo.ru/upload/kr/HOBL_2023_draft.pdf.; Malerba M, Foci V, Patrucco F, Pochetti P, Nardin M, Pelaia C, Radaeli A. Single Inhaler LABA/LAMA for COPD. Front Pharmacol. 2019;10:390. https://doi.org/10.3389/fphar.2019.00390.; Melani AS, Croce S, Fabbri G, Messina M, Bargagli E. Inhaled Corticosteroids in Subjects with Chronic Obstructive Pulmonary Disease: An Old, Unfinished History. Biomolecules. 2024;14(2):195. https://doi.org/10.3390/biom14020195.; Авдеев СН, Лещенко ИВ, Айсанов ЗР, Архипов ВВ, Белевский АС, Овчаренко СИ и др. Новые клинические рекомендации по ХОБЛ - смена парадигмы. Терапевтический архив. 2024;96(3):292-297. https://doi.org/10.26442/00403660.2024.03.202646.; Banerji D, Fogel R, Patalano F. Indacaterol/glycopyrronium: a dual bron-chodilator for COPD. Drug Discov Today. 2018;23(1):196-203. https://doi.org/10.1016/j.drudis.2017.10.015.; Frampton JE. QVA149 (indacaterol/glycopyrronium fixed-dose combination): a review of its use in patients with chronic obstructive pulmonary disease. Drugs. 2014;74(4):465-488. https://doi.org/10.1007/s40265-014-0194-8.; Sanders MJ. Guiding Inspiratory Flow: Development of the In-Check DIAL G16, a Tool for Improving Inhaler Technique. Pulm Med. 2017;2017:1495867. https://doi.org/10.1155/2017/1495867.; Dolovich MB, Kuttler A, Dimke TJ, Usmani OS. Biophysical model to predict lung delivery from a dual bronchodilator dry-powder inhaler. Int J Pharm X. 2019;1:100018. https://doi.org/10.1016/j.ijpx.2019.100018.

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    Academic Journal

    Πηγή: Meditsinskiy sovet = Medical Council; № 20 (2024); 10-16 ; Медицинский Совет; № 20 (2024); 10-16 ; 2658-5790 ; 2079-701X

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.med-sovet.pro/jour/article/view/8747/7679; Fragoso E, Andre S, Boleo-Tome JP, Areias V, Munha J, Cardoso J. Understanding COPD: A vision on phenotypes, comorbidities and treatment approach. GI COPD - Interest Group on Chronic Obstructive Pulmonary Disease. Rev Port Pneumol (2006). 2016;22(2):101-111. https://doi.org/10.1016/j.rppnen.2015.12.001.; Pavord ID. Biologics and chronic obstructive pulmonary disease. J Allergy Clin Immunol. 2018;141(6):1983-1991. https://doi.org/10.1016/j.jaci.2018.04.020.; Brightling CE. Chronic obstructive pulmonary disease phenotypes, biomarkers, and prognostic indicators. Allergy Asthma Proc. 2016;37(6):432-438. https://doi.org/10.2500/aap.2016.37.3996.; Barnes PJ. Inflammatory mechanisms in patients with chronic obstructive pulmonary disease. J Allergy Clin Immunol. 2016;138(1):16-27. https://doi.org/10.1016/j.jaci.2016.05.011.; Brightling C, Greening N. Airway inflammation in COPD: progress to precision medicine. Eur Respir J. 2019;54(2):1900651. https://doi.org/10.1183/13993003.00651-2019.; Landis S, Suruki R, Maskell J, Bonar K, Hilton E, Compton C. Demographic and Clinical Characteristics of COPD Patients at Different Blood Eosinophil Levels in the UK Clinical Practice Research Datalink. COPD. 2018;15(2):177-184. https://doi.org/10.1080/15412555.2018.1441275.; Pascoe S, Locantore N, Dransfield MT, Barnes NC, Pavord ID. Blood eosinophil counts, exacerbations, and response to the addition of inhaled fluticasone furoate to vilanterol in patients with chronic obstructive pulmonary disease: a secondary analysis of data from two parallel randomised controlled trials. Lancet Respir Med. 2015;3(6):435-442. https://doi.org/10.1016/S2213-2600(15)00106-X.; Singh D, Kolsum U, Brightling CE, Locantore N, Agusti A, Tal-Singer R. Eosinophilic inflammation in COPD: prevalence and clinical characteristics. Eur Respir J. 2014;44(6):1697-1700. https://doi.org/10.1183/09031936.00162414.; George L, Brightling CE. Eosinophilic airway inflammation: role in asthma and chronic obstructive pulmonary disease. Ther Adv Chronic Dis. 2016;7(1):34-51. https://doi.org/10.1177/2040622315609251.; Авдеев СН, Трушенко НВ, Мержоева ЗМ, Иванова МС, Кусраева ЭВ. Эозинофильное воспаление при хронической обструктивной болезни легких. Терапевтический архив. 2019;91(10):144-152. https://doi.org/10.26442/00403660.2019.10.000426.; Brusselle G, Pavord ID, Landis S, Pascoe S, Lettis S, Morjaria N et al. Blood eosinophil levels as a biomarker in COPD. Respir Med. 2018;138:21-31. https://doi.org/10.1016/j.rmed.2018.03.016.; Eltboli O, Bafadhel M, Hollins F, Wright A, Hargadon B, Kulkarni N, Brightling C. COPD exacerbation severity and frequency is associated with impaired macrophage efferocytosis of eosinophils. BMC Pulm Med. 2014;14:112. https://doi.org/10.1186/1471-2466-14-112.; Kolsum U, Damera G, Pham TH, Southworth T, Mason S, Karur P et al. Pulmonary inflammation in patients with chronic obstructive pulmonary disease with higher blood eosinophil counts. J Allergy Clin Immunol. 2017;140(4):1181-1184.e7. https://doi.org/10.1016/j.jaci.2017.04.027.; Bhatt SP, Rabe KF, Hanania NA, Vogelmeier CF, Bafadhel M, Christenson SA et al. Dupilumab for COPD with Blood Eosinophil Evidence of Type 2 Inflammation. N Engl J Med. 2024;390(24):2274-2283. https://doi.org/10.1056/NEJMoa2401304.; Hogg JC, Chu F, Utokaparch S, Woods R, Elliott WM, Buzatu L et al. The nature of small-airway obstruction in chronic obstructive pulmonary disease. N Engl J Med. 2004;350(26):2645-2653. https://doi.org/10.1056/NEJMoa032158.; Turato G, Semenzato U, Bazzan E, Biondini D, Tine M, Torrecilla N et al. Blood Eosinophilia Neither Reflects Tissue Eosinophils nor Worsens Clinical Outcomes in Chronic Obstructive Pulmonary Disease. Am J Respir Crit Care Med. 2018;197(9):1216-1219. https://doi.org/10.1164/rccm.201708-1684LE.; Hastie AT, Martinez FJ, Curtis JL, Doerschuk CM, Hansel NN, Christenson S et al. Association of sputum and blood eosinophil concentrations with clinical measures of COPD severity: an analysis of the SPIROMICS cohort. Lancet Respir Med. 2017;5(12):956-967. https://doi.org/10.1016/S2213-2600(17)30432-0.; Cheng SL, Lin CH. Effectiveness using higher inhaled corticosteroid dosage in patients with COPD by different blood eosinophilic counts. Int J Chron Obstruct Pulmon Dis. 2016;11:2341-2348. https://doi.org/10.2147/COPD.S115132.; Kerkhof M, Freeman D, Jones R, Chisholm A, Price DB. Predicting frequent COPD exacerbations using primary care data. Int J Chron Obstruct Pulmon Dis. 2015;10:2439-2450. https://doi.org/10.2147/COPD.S94259.; Siva R, Green RH, Brightling CE, Shelley M, Hargadon B, McKenna S et al. Eosinophilic airway inflammation and exacerbations of COPD: a randomised controlled trial. Eur Respir J. 2007;29(5):906-913. https://doi.org/10.1183/09031936.00146306.; Couillard S, Larivee P, Courteau J, Vanasse A. Eosinophils in COPD Exacerbations Are Associated With Increased Readmissions. Chest. 2017;151(2):366-373. https://doi.org/10.1016/j.chest.2016.10.003.; Mullerova H, Meeraus WH, Galkin DV, Albers FC, Landis SH. Clinical burden of illness among patients with severe eosinophilic COPD. Int J Chron Obstruct Pulmon Dis. 2019;14:741-755. https://doi.org/10.2147/COPD.S194511.; Criner GJ, Celli BR, Brightling CE, Agusti A, Papi A, Singh D et al. Benralizumab for the Prevention of COPD Exacerbations. N Engl J Med. 2019;381(11):1023-1034. https://doi.org/10.1056/NEJMoa1905248.; Lommatzsch M, Mohme SN, Stoll P, Virchow JC. Response to Various Biologics in Patients with Both Asthma and Chronic Obstructive Pulmonary Disease. Respiration. 2023;102(12):986-990. https://doi.org/10.1159/000534922.; Bhatt SP, Rabe KF, Hanania NA, Vogelmeier CF, Cole J, Bafadhel M et al. Dupilumab for COPD with Type 2 Inflammation Indicated by Eosinophil Counts. N Engl J Med. 2023;389(3):205-214. https://doi.org/10.1056/NEJMoa2303951.; Castro M, Corren J, Pavord ID, Maspero J, Wenzel S, Rabe KF et al. N Engl J Med. 2018;378(26):2486-2496. https://doi.org/10.1056/NEJMoa1804092.

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    Academic Journal
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    Academic Journal

    Πηγή: Meditsinskiy sovet = Medical Council; № 20 (2023); 10-17 ; Медицинский Совет; № 20 (2023); 10-17 ; 2658-5790 ; 2079-701X

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.med-sovet.pro/jour/article/view/7877/6992; Авдеев СН, Айсанов ЗР, Ардашева ТВ, Белевский АС, Демко ИВ, Зайцев АА и др. Хроническая обструктивная болезнь легких: клинические рекомендации. 2023. 100 с. Режим доступа: https://spulmo.ru/upload/kr/HOBL_2023_draft.pdf.; Авдеев СН, Айсанов ЗР, Архипов ВВ, Белевский АС, Визель АА, Демко ИВ и др. Назначение/отмена ингаляционных глюкокортикостероидов у больных хронической обструктивной болезнью легких как терапевтический континуум в реальной клинической практике. Пульмонология. 2023;33(1):109–118. https://doi.org/10.18093/0869-0189-202333-1-109-118.; Авдеев СН, Невзорова ВА, Куделя ЛМ, Кондрашова НМ, Суханова ГИ, Киняйкин МФ и др. Вопросы тройной терапии в лечении хронической обструктивной болезни легких. Комментарии к алгоритму. Резолюция Совета экспертов от 13.06.18 (Владивосток). Пульмонология. 2019;29(3):365–374. https://doi.org/10.18093/0869-0189-2019-29-3-365-374.; Calzetta L, Matera MG, Rogliani P, Cazzola M. The role of triple therapy in the management of COPD. Expert Rev Clin Pharmacol. 2020;13(8):865–874. https://doi.org/10.1080/17512433.2020.1787830.; Ferguson GT, Rabe KF, Martinez FJ, Fabbri LM, Wang C, Ichinose M et al. Triple therapy with budesonide/glycopyrrolate/formoterol fumarate with co-suspension delivery technology versus dual therapies in chronic obstructive pulmonary disease (KRONOS): a double-blind, parallel-group, multicentre, phase 3 randomised controlled trial. Lancet Respir Med. 2018;6(10):747–758. https://doi.org/10.1016/S2213-2600(18)30327-8.; Martinez FJ, Rabe KF, Ferguson GT, Wedzicha JA, Trivedi R, Jenkins M et al. Benefits of budesonide/glycopyrrolate/formoterol fumarate (BGF) on symptoms and quality of life in patients with COPD in the ETHOS trial. Respir Med. 2021;185:106509. https://doi.org/10.1016/j.rmed.2021.106509.; Ishiura Y, Fujimura M, Ohkura N, Hara J, Kasahara K, Ishii N et al. Triple Therapy with Budesonide/Glycopyrrolate/Formoterol Fumarate Improves Inspiratory Capacity in Patients with Asthma-Chronic Obstructive Pulmonary Disease Overlap. Int J Chron Obstruct Pulmon Dis. 2020;15:269–277. https://doi.org/10.2147/COPD.S231004.; Rabe KF, Martinez FJ, Ferguson GT, Wang C, Singh D, Wedzicha JA et al. Triple Inhaled Therapy at Two Glucocorticoid Doses in Moderate-to-VerySevere COPD. N Engl J Med. 2020;383(1):35–48. https://doi.org/10.1056/NEJMoa1916046.; Singh D, Rabe KF, Martinez FJ, Krüll M, Jenkins M, Patel M, Dorinsky P. Relationship between prior inhaled corticosteroid use and benefits ofbudesonide/glycopyrronium/formoterol fumarate dihydrate on exacerbations, symptoms, health-related quality of life, and lung function in patients with chronic obstructive pulmonary disease: Analyses from the ETHOS study. Respir Med. 2022;197:106857. https://doi.org/10.1016/j.rmed.2022.106857.; Martinez FJ, Rabe KF, Ferguson GT, Wedzicha JA, Singh D, Wang C et al. Reduced All-Cause Mortality in the ETHOS Trial of Budesonide/Glycopyrrolate/ Formoterol for Chronic Obstructive Pulmonary Disease. A Randomized, Double-Blind, Multicenter, Parallel-Group Study. Am J Respir Crit Care Med. 2021;203(5):553–564. https://doi.org/10.1164/rccm.202006-2618OC.; Kolsum U, Damera G, Pham TH, Southworth T, Mason S, Karur P et al. Pulmonary inflammation in patients with chronic obstructive pulmonary disease with higher blood eosinophil counts. J Allergy Clin Immunol. 2017;140(4):1181–1184. https://doi.org/10.1016/j.jaci.2017.04.027.; Hasegawa K, Camargo CAJr. Prevalence of blood eosinophilia in hospitalized patients with acute exacerbation of COPD. Respirology. 2016;21(4):761–764. https://doi.org/10.1111/resp.12724.; Landis S, Suruki R, Maskell J, Bonar K, Hilton E, Compton C. Demographic and Clinical Characteristics of COPD Patients at Different Blood Eosinophil Levels in the UK Clinical Practice Research Datalink. COPD. 2018;15(2):177–184. https://doi.org/10.1080/15412555.2018.1441275.; Bacci E, Cianchetti S, Bartoli M, Dente FL, Di Franco A, Vagaggini B, Paggiaro P. Low sputum eosinophils predict the lack of response to beclomethasone in symptomatic asthmatic patients. Chest. 2006;129(3):565–572. https://doi.org/10.1378/chest.129.3.565.; Pizzichini E, Pizzichini MM, Gibson P, Parameswaran K, Gleich GJ, Berman L et al. Sputum eosinophilia predicts benefit from prednisone in smokers with chronic obstructive bronchitis. Am J Respir Crit Care Med. 1998;158(5):1511–1517. https://doi.org/10.1164/ajrccm.158.5.9804028.; Park HY, Lee H, Koh WJ, Kim S, Jeong I, Koo HK et al. Association of blood eosinophils and plasma periostin with FEV1 response after 3-month inhaled corticosteroid and long-acting beta2-agonist treatment in stable COPD patients. Int J Chron Obstruct Pulmon Dis. 2015;11:23–30. https://doi.org/10.2147/COPD.S94797.; Авдеев СН, Трушенко НВ, Мержоева ЗМ, Иванова МС, Кусраева ЭВ. Эозинофильное воспаление при хронической обструктивной болезни легких. Терапевтический архив. 2019;91(10):144–152. https://doi.org/10.26442/00403660.2019.10.000426.; Лещенко ИВ, Мещерякова АС. Современные возможности терапии ингаляционными глюкокортикостероидами пациентов с хронической обструктивной болезнью легких. Пульмонология. 2021;31(1):75–87. https://doi.org/10.18093/0869-0189-2021-31-1-75-87.; Bafadhel M, Rabe KF, Martinez FJ, Singh D, Darken P, Jenkins M et al. Benefits of Budesonide/Glycopyrronium/Formoterol Fumarate Dihydrate on COPD Exacerbations, Lung Function, Symptoms, and Quality of Life Across Blood Eosinophil Ranges: A Post-Hoc Analysis of Data from ETHOS. Int J Chron Obstruct Pulmon Dis. 2022;17:3061–3073. https://doi.org/10.2147/COPD.S374670.; Muro S, Sugiura H, Darken P, Dorinsky P. Efficacy of budesonide/glycopyrronium/formoterol metered dose inhaler in patients with COPD: post-hoc analysis from the KRONOS study excluding patients with airway reversibility and high eosinophil counts. Respir Res. 2021;22(1):187. https://doi.org/10.1186/s12931-021-01773-1.; Marsh SE, Travers J, Weatherall M, Williams MV, Aldington S, Shirtcliffe PM et al. Proportional classification of COPD phenotypes. Thorax. 2008;63(9):761–767. https://doi.org/10.1136/thx.2007.089193.; Shaya FT, Dongyi D, Akazawa MO, Blanchette CM, Wang J, Mapel DW et al. Burden of concomitant asthma and COPD in a Medicaid population. Chest. 2008;134(1):14–19. https://doi.org/10.1378/chest.07-2317.; Hardin M, Silverman EK, Barr RG, Hansel NN, Schroeder JD, Make BJ et al. The clinical features of the overlap between COPD and asthma. Respir Res. 2011;12(1):127. https://doi.org/10.1186/1465-9921-12-127.; Park SY, Kim S, Kim JH, Kim SH, Lee T, Yoon SY et al. A Randomized, Noninferiority Trial Comparing ICS + LABA with ICS + LABA + LAMA in Asthma-COPD Overlap (ACO) Treatment: The ACO Treatment with Optimal Medications (ATOMIC) Study. J Allergy Clin Immunol Pract. 2021;9(3):1304–1311. https://doi.org/10.1016/j.jaip.2020.09.066.; Lipson DA, Barnhart F, Brealey N, Brooks J, Criner GJ, Day NC et al. Once-Daily Single-Inhaler Triple versus Dual Therapy in Patients with COPD. N Engl J Med. 2018;378(18):1671–1680. https://doi.org/10.1056/NEJMoa1713901.; Papi A, Vestbo J, Fabbri L, Corradi M, Prunier H, Cohuet G et al. Extrafine inhaled triple therapy versus dual bronchodilator therapy in chronic obstructive pulmonary disease (TRIBUTE): a double-blind, parallel group, randomised controlled trial. Lancet. 2018;391(10125):1076–1084. https://doi.org/10.1016/S0140-6736(18)30206-X.; Izquierdo JL, Cosio BG. The dose of inhaled corticosteroids in patients with COPD: when less is better. Int J Chron Obstruct Pulmon Dis. 2018;13:3539–3547. https://doi.org/10.2147/COPD.S175047.; Donaldson GC, Seemungal TA, Bhowmik A, Wedzicha JA. Relationship between exacerbation frequency and lung function decline in chronic obstructive pulmonary disease. Thorax. 2002;57(10):847–852. https://doi.org/10.1136/thorax.57.10.847.; Cazzola M, Rogliani P, Laitano R, Calzetta L, Matera MG. Beyond Dual Bronchodilation – Triple Therapy, When and Why. Int J Chron Obstruct Pulmon Dis. 2022;17:165–180. https://doi.org/10.2147/COPD.S345263.

  15. 15
    Academic Journal

    Πηγή: Туберкулез, легочные болезни, ВИЧ-инфекция; № 1 (2020); 69-77
    Туберкульоз, легеневі хвороби, ВІЛ-інфекція; № 1 (2020); 69-77
    Tuberculosis, Lung Diseases, HIV Infection; № 1 (2020); 69-77

    Περιγραφή αρχείου: application/pdf

    Σύνδεσμος πρόσβασης: http://tubvil.com.ua/article/view/198955

  16. 16
    Academic Journal

    Πηγή: Messenger of ANESTHESIOLOGY AND RESUSCITATION; Том 20, № 2 (2023); 78-84 ; Вестник анестезиологии и реаниматологии; Том 20, № 2 (2023); 78-84 ; 2541-8653 ; 2078-5658

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.vair-journal.com/jour/article/view/752/630; https://www.vair-journal.com/jour/article/downloadSuppFile/752/245; Заболотских И. Б. Периоперационное ведение пациентов с нервно-мышечными заболеваниями (проект клинических рекомендаций ФАР России) / И. Б. Заболотских [и др.] // Регионарная анестезия и лечение острой боли. – 2014. – Т. 8, № 2. – C. 58–75.; Карамян Р. А. Злокачественная гипертермия / Р. А. Карамян // Здоровье и образование в XXI веке. – 2016. – № 1. – C. 157–161.; Ким Е. С. Злокачественная гипертермия: современные подходы к профилактике и лечению / Е. С. Ким, В. И. Горбачев, В. В. Унжаков // ActaBiomedicaScientifica. – 2017. – Т. 2, № 5 (2). – C. 154–158. doi:10.12737/article_5a3a0ef02e9901.72007754.; Киреев С. С. Злокачественная гипертермия / С. С. Киреев, О. С. Бериашвили // Вестник новых медицинских технологий. – 2018. – Т. 12, № 2. – С. 33–41. doi:10.24411/2075-4094-2018-16012.; Прокопьев Г. Г. Современные взгляды на синдром злокачественной гипертермии [Электронный ресурс] / Г. Г. Прокопьев, В. А. Михельсон, Э. Г. Агавелян // Медицина неотложных состояний. – 2011. – Т. 7–8, № 38–39. URL: http://www.mif-ua.com/archive/article/24197?ysclid=lhpwq011t1271182719 (дата обращения 15. 03. 2023).; Cieniewicz A., Trzebicki I. J., Mayzner-Zawadzka E., Koste ra-Pruszczyk A., Owczuk R. Malignant hyperthermia – what do we know in 2019? // Anaesthesiol Intensive Therapy. – 2019. – Vol. 51, № 3. – P. 169–177. doi:10.5114/ait.2019.87646.; Gong X. Malignant hyperthermia when dantrolene is not readily available // BMC Anesthesiology. – 2021. – Vol. 21. – P. 1–11. doi:10.1186/s12871-021-01328-3.; Glahn K. P., Ellis F. R., Halsall P. J. et al. Recognizing and managing a malignant hyperthermia crisis: guidelines from the European Malignant Hyperthermia Group //British Journal of Anaesthesia. – 2010. – Vol. 105, № 4. – P. 417–420. doi:10.1093/bja/aeq243.; Hopkin T., Girard S., Dalay B. et al. Malignant hyperthermia 2020 Guideline from the Association of Anaesthetists // Anaesthesia. – 2021. – Vol. 76. – P. 655–664. doi:10.1111/anae.15317.; Horstick E. J. et al. Stac3 is a component of the excitation–contraction coupling machinery and mutated in Native American myopathy // Nature Communications. – 2013. – № 4. – P. 1952. doi:10.1038/ncomms2952.; Kim D. C. Malignant hyperthermia. // Korean Journal of Anesthesiology. –2012. – Vol. 63, № 5. – P. 391–401. doi:10.4097/kjae.2012.63.5.391.; Kim J. H., Lee C. K., Chung C. E., Min B. D., Kim D. C. Malignant hyperthermia: a case report with a literature review. // Archives of Aesthetic Plastic Surgery. – 2022. – Vol. 28, № 2. – P. 75–78. doi: https://doi.org/10.14730/aaps.2022.00395; Klingler W., Roewer N., Schuster F., Wappler F. S1-Leitlinie: Therapie der malignen Hyperthermie // Deutsche Gesellschaft für Anästhesiologie und Intensivmedizin. – 2018. – Vol. 59. – P. 204–208.; Larach M. G. A Primer for Diagnosing and Managing Malignant Hyperthermia Susceptibility. //Anesthesiology. – 2018. – Vol. 128. – P. 8–10. doi:10.1097/ALN.0000000000001879.; Levitt R. C. Prospects for the diagnosis of malignant hyperthermia susceptibility using molecular genetic approaches //Anesthesiology. – 1992. – Vol. 76. – P. 1039–1048. doi:10.1097/00000542-199206000-00025.; Litman R. S., Griggs S. M., Dowling J. J., Riazi S. Malignant hyperthermia susceptibility and related diseases. //Anesthesiology. – 2018. – Vol. 128. – P. 159–167. doi:10.1097/ALN.0000000000001877.; Litman R. S., Smith V. I., Larach M. G. et al. Consensus Statement of the Malignant Hyperthermia Association of the United States on Unresolved Clinical Questions Concerning the Management of Patients With Malignant Hyperthermia // Anesthesia & Analgesia. – 2019. – Vol. 128, № 4. – P. 652–659. doi:10.1213/ANE.0000000000004039.; Linsley J. W., Hsu I.-U., Groom L. et al. Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3 // Proceedings of the National Academy of Sciences (Proceedings of the National Academy of Sciences of the United States of America). – 2017. – Vol. 114, № 2. – Р. 228–236. doi:10.1073/pnas.1619238114.; Mayhew J. F., Rudolph J., Tobey R. E. Malignant hyperthermia in a six month old infant: a case report //Anesthesia & Analgesia. – 1978. – Vol. 57, № 2. – P. 262–264. doi:10.1213/00000539-197803000-00018.; MacLennan D. H., Phillips M. S. Malignant hyperthermia // Science. – 1992. – Vol. 256, № 5058. – P. 789–794. doi:10.1126/science.1589759.; Perszke M., Egierska D., Cieślak K. et al. Malignant hyperthermia – state of knowledge. // Journal of Education, Health and Sport. – 2022. - Vol.1, № 9. – P. 883–890. doi:10.12775/JEHS.2022.12.09.102.; Riazi S., Kraeva N., Hopkins P. M. Malignant Hyperthermia in the Post-Genomics Era New Perspectives on an Old Concept // Anesthesiology. – 2018. – Vol. 128. – P. 168–80. doi:10.1097/ALN.0000000000001878.; Riazi S., Larach M. G., Hu C., Wijeysundera D., Massey C., Kraeva N. Malignant hyperthermia in Canada: characteristics ofindex anesthetics in 129 malignant hyperthermia susceptibleprobands // Anesthesia & Analgesia. – 2014. – Vol. 118. – P. 381–387. doi:10.1213/ANE.0b013e3182937d8b.; Rosenberg H., Davis M., James D., Pollock N., Stowell К. Malignant hyperthermia // Orphanet Journal of Rare Diseases. – 2007. – Vol. 2, № 21. – P. 1750–1772. doi:10.1186/1750-1172-2-21.; Rosenberg H., Pollock N., Schiemann A., Bulger T., Stowell K. Malignant hyperthermia: a review // Orphanet Journal of Rare Diseases. – 2015. – Vol. 10, № 1. – P. 1–19. doi:10.1186/s13023-015-0310-1.; Ruffert H., Bastian B., Bendixen D. et al. Consensus guidelines on perioperative management of malignant hyperthermia suspected or susceptible patients from the European Malignant Hyperthermia Group // British Journal of Anaesthesia. – 2021. – Vol. 126, № 1. – Р. 120–130. doi:10.1016/j.bja.2020.09.029.

  17. 17
    Academic Journal

    Πηγή: Meditsinskiy sovet = Medical Council; № 20 (2023); 28-35 ; Медицинский Совет; № 20 (2023); 28-35 ; 2658-5790 ; 2079-701X

    Περιγραφή αρχείου: application/pdf

    Relation: https://www.med-sovet.pro/jour/article/view/7883/6997; Johnson M, Rennard S. Alternative mechanisms for long-acting beta(2)-adrenergic agonists in COPD. Chest. 2001;120(1):258–270. https://doi.org/10.1378/chest.120.1.258.; Paggiaro PL, Giannini D, Di Franco A, Testi R. Comparison of inhaled salmeterol and individually dose-titrated slow-release theophylline in patients with reversible airway obstruction. European Study Group. Eur Respir J. 1996;9(8):1689–1695. https://doi.org/10.1183/09031936.96.09081689.; Perera BJ. Salmeterol multicentre asthma research trial (SMART): interim analysis shows increased risk of asthma related deaths. Ceylon Med J. 2003;48(3):99. https://doi.org/10.4038/cmj.v48i3.3362.; Williams C. Cause of death in the SMART Trial. Chest. 2006;130(3):929–930. https://doi.org/10.1378/chest.130.3.929-a.; Визель АА, Визель ИЮ. Хроническая обструктивная болезнь легких – от истоков к современности (исторический обзор литературы). Туберкулез и болезни легких. 2019;97(2):42–49. https://doi.org/10.21292/2075-1230-2019-97-2-42-49.; Чучалин АГ, Авдеев СН, Айсанов ЗР, Белевский АС, Васильева ОС, Геппе НА и др. Бронхиальная астма: федеральные клинические рекомендации по диагностике и лечению. Пульмонология. 2022;32(3):393–447. https://doi.org/10.18093/0869-0189-2022-32-3-393-447.; Reddel HK, Bateman ED, Schatz M, Krishnan JA, Cloutier MM. A Practical guide to implementing SMART in asthma management. J Allergy Clin Immunol Pract. 2022;10(1 Suppl.):31–38. https://doi.org/10.1016/j.jaip.2021.10.011.; Ненашева НМ. Концепция «противовоспалительный бронхолитик»: гармония между потребностями пациента и целями врача при бронхиальной астме любой степени тяжести. Практическая аллергология. 2021;(1):8–16. https://doi.org/10.46393/2712-9667_2021_1_8-16.; Демко ИВ, Мамаева МГ, Собко ЕА, Крапошина АЮ, Гордеева НВ. Клинический опыт применения будесонида/формотерола у пациентов с хронической обструктивной болезнью легких. Медицинский совет. 2021;(16):26–31. https://doi.org/10.21518/2079-701X-2021-16-26-31.; Aryani T, Rahmawati RK, Cintyadewi NP, Puspitasari AD, Rasyid AN, Samirah. Patterns of bronchodilator therapy in asthmatic outpatients. J Public Health Afr. 2023;14(Suppl. 1):2533. https://doi.org/10.4081/jphia.2023.2533.; Vinnikov D, Raushanova A, Mukatova I, Nurpeissov T, Кushekbayeva A, Toxarina A et al. Asthma control in Kazakhstan: need for urgent action. BMC Pulm Med. 2023;23(1):7. https://doi.org/10.1186/s12890-022-02287-2.; Nishi MK, Akter S, Tania IJ, Shams N, Khatun S. Use of Drugs considering route of administration on drug prescription pattern for bronchial asthma in a tertiary level hospital. Mymensingh Med J. 2023;32(1):73–75. Available at: https://pubmed.ncbi.nlm.nih.gov/36594304.; Salciccioli JD, Israel E. As-needed inhaled corticosteroids as add-on therapy versus SMART therapy: an evolving understanding of the two approaches in the management of moderate-to-severe asthma. Curr Opin Pulm Med. 2023;29(3):209–214. https://doi.org/10.1097/MCP.0000000000000961.; Larenas-Linnemann D, Romeo J, Ariue B, Oppenheimer J. American College of Allergy, Asthma and Immunology members’ preferred steps 1 to 3 asthma maintenance and reliever therapy and incomplete insurance coverage indicated as main practice hurdle. Ann Allergy Asthma Immunol. 2023;131(4):451–457. https://doi.org/10.1016/j.anai.2023.05.036.; Krings JG, Sekhar TC, Chen V, Blake KV, Sumino K, James AS et al. Beginning to address an implementation gap in asthma: clinicians’ views of prescribing reliever budesonide-formoterol inhalers and SMART in the United States. J Allergy Clin Immunol Pract. 20023;11(9):2767–2777. https://doi.org/10.1016/j.jaip.2023.05.023.; Janson C, Melén E, de Fine Licht S, Telg G, Maslova E, Tran TN et al. Prescribing patterns of budesonide/formoterol maintenance and reliever therapy in patients with asthma in Sweden. Allergy. 2023;78(8):2311–2314. https://doi.org/10.1111/all.15710.; Günaydın FE, Ay P, Karakaya G, Ediger D. How do we manage asthma? Assessment of knowledge, attitude, and practice patterns among pulmonologists and allergists. J Asthma. 2023;60(1):130–138. https://doi.org/10.1080/02770903.2022.2033261.; Czira A, Banks V, Requena G, Wood R, Tritton T, Wild R et al. Characterisation of patients with chronic obstructive pulmonary disease initiating single-device inhaled corticosteroids/long-acting β2 -agonist dual therapy in a primary care setting in England. BMJ Open Respir Res. 2022;9(1):e001243. https://doi.org/10.1136/bmjresp-2022-001243.; Brattsand R, Selroos O. May a different kinetic mode explain the high efficacy/safety profile of inhaled budesonide? Pulm Pharmacol Ther. 2022;77:102167. https://doi.org/10.1016/j.pupt.2022.102167.; Varacca G, D’Angelo D, Glieca S, Cavalieri L, Piraino A, Quarta E et al. The impact of possible improper use on the performance in vitro of NEXThaler in comparison with Ellipta inhaler. Eur J Pharm Sci. 2023;183:106385. https://doi.org/10.1016/j.ejps.2023.106385.; Renner A, Marth K, Breyer-Kohansal R, Pohl W. Combined analysis of five non-interventional studies of the effectiveness, tolerability, and safety of the extrafine fixed dose beclomethasone/formoterol combination in the treatment of asthma in Austria. Respir Med. 2023;207:107097. https://doi.org/10.1016/j.rmed.2022.107097.; Титова ОН, Кузубова НА, Лебедева ЕС, Преображенская ТН. Эффект применения экстрамелкодисперсной комбинации беклометазон/формотерол на ранней стадии формирования модели ХОБЛ. РМЖ. 2022;(2):16–20. Режим доступа: https://www.rmj.ru/articles/bolezni_dykhatelnykh_putey/Effekt_primeneniya_ekstramelkodispersnoy_kombinacii_beklometazonformoterol_naranney_stadii_formirovaniya_modeli_HOBL.; Метельский СМ, Давидовская ЕИ, Нагорнов ИВ, Ермолкевич РФ, Богуш ЛС, Рузанов ДЮ, Воробьева ОИ. Место ингаляционных кортикостероидных препаратов в комплексной терапии ХОБЛ с позиций GOLD-2022. Рецепт. 2022;25(5):660–673. https://doi.org/10.34883/PI.2022.25.5.009.; Bakakos P, Chatziapostolou P, Katerelos P, Efstathopoulos P, Korkontzelou A, Katsaounou P. Extrafine beclometasone dipropionate/formoterol nexthaler on device usability, adherence, asthma control and quality of life. A panhellenic prospective, non-interventional observational study in patients with asthma-the NEXT-Step Study. J Pers Med. 2022;12(2):146. https://doi.org/10.3390/jpm12020146.; Luo Z, Lucci G, Santoro L, Topole E, Mariotti F. Pharmacokinetic profile of beclometasone dipropionate/formoterol fumarate administered through a novel dry-powder inhaler in Chinese healthy volunteers. Pulm Pharmacol Ther. 2022;73–74:102129. https://doi.org/10.1016/j.pupt.2022.102129.; Reddel HK, Brusselle G, Lamarca R, Gustafson P, Anderson GP, Jorup C. Safety and effectiveness of as-needed formoterol in asthma patients taking inhaled corticosteroid (ics)-formoterol or ics-salmeterol maintenance therapy. J Allergy Clin Immunol Pract. 2023;11(7):2104-2114.e3. https://doi.org/10.1016/j.jaip.2023.03.046.; Muiser S, Imkamp K, Seigers D, Halbersma NJ, Vonk JM, Luijk BHD et al. Budesonide/formoterol maintenance and reliever therapy versus fluticasone/salmeterol fixed-dose treatment in patients with COPD. Thorax. 2023;78(5):451–458. https://doi.org/10.1136/thorax-2022-219620.; Price DB, Henley W, Cançado JED, Fabbri LM, Kerstjens HAM, Papi A et al. Interclass difference in pneumonia risk in copd patients initiating fixed dose inhaled treatment containing extrafine particle beclometasone versus fine particle fluticasone. Int J Chron Obstruct Pulmon Dis. 2022;17:355–370. https://doi.org/10.2147/COPD.S342357.; Jiang T, Li P, Wang Y. Effect of budesonide formoterol combined with tiotropium bromide on pulmonary function and inflammatory factors in patients with asthma-COPD overlap syndrome. Allergol Immunopathol (Madr). 2023;51(4):131–138. https://doi.org/10.15586/aei.v51i4.876.; Samajdar SS, Mukherjee S, Moitra S, Pal J, Joshi S, Tripathi SK. Effectiveness of budesonide formoterol fixed-dose combination MDI in reducing cough symptoms in COVID-19 patients: A real-world evidence study. Lung India. 2023;40(2):107–111. https://doi.org/10.4103/lungindia.lungindia_268_22.; van der Veer T, de Koning Gans JM, Braunstahl GJ, Pieters ALP, van den Berg JMW, Hoek RAS et al. The effect of beclomethasone-formoterol versus placebo on chronic cough in patients with non-CF bronchiectasis: the FORZA randomised controlled trial. Eur Respir J. 2023;61(6):2300186. https://doi.org/10.1183/13993003.00186-2023.; Maneechotesuwan K, Singh D, Fritscher LG, Dursunoglu NPGA, Phansalkar A, Aggarwal B et al. Impact of inhaled fluticasone propionate/salmeterol on health-related quality of life in asthma: A network meta-analysis. Respir Med. 2022;203:106993. https://doi.org/10.1016/j.rmed.2022.106993.; Hale EM, Greene G, Mulvey C, Mokoka MC, van Boven JFM, Cushen B et al.; INCA Research Team. Use of digital measurement of medication adherence and lung function to guide the management of uncontrolled asthma (INCA Sun): a multicentre, single-blinded, randomised clinical trial. Lancet Respir Med. 2023;11(7):591–601. https://doi.org/10.1016/S2213-2600(22)00534-3.; Doniec Z, Olszanecka-Glinianowicz M, Hantulik P, Almgren-Rachtan A, Chudek J. The assessment of effectiveness, tolerance, and patient satisfaction with the use of a new fixed-dose combination product, containing salmeterol and fluticasone propionate, Salflumix Easyhaler® in the treatment of asthma in the daily clinical practice. J Asthma. 2023;60(4):754–760. https://doi.org/10.1080/02770903.2022.2093220.; Feldman WB, Kesselheim AS, Avorn J, Russo M, Wang SV. Comparative effectiveness and safety of generic versus brand-name fluticasonesalmeterol to treat chronic obstructive pulmonary disease. Ann Intern Med. 2023;176(8):1047–1056. https://doi.org/10.7326/M23-0615.; Alyami MH, Dahmash EZ, Ali DK, Alyami HS, AbdulKarim H, Alsudir SA. Novel fluticasone propionate and salmeterol fixed-dose combination nano-encapsulated particles using polyamide based on L-Lysine. Pharmaceuticals (Basel). 2022;15(3):321. https://doi.org/10.3390/ph15030321.; Mills H, Acquah R, Tang N, Cheung L, Klenk S, Glassen R et al. Biochemical behaviours of salmeterol/fluticasone propionate in treating asthma and chronic obstructive pulmonary diseases (COPD). Emerg Med Int. 2022;2022:2593740. https://doi.org/10.1155/2022/2593740.

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    Πηγή: Tuberculosis and Lung Diseases; Том 100, № 1 (2022); 7-18 ; Туберкулез и болезни легких; Том 100, № 1 (2022); 7-18 ; 2542-1506 ; 2075-1230

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    Relation: https://www.tibl-journal.com/jour/article/view/1601/1610; Арутюнов Г. П., Тарловская Е. И., Арутюнов А. Г., Беленков Ю. Н., Конради А. О., Лопатин Ю. М., Ребров А. П. и др. Анализ влияния препаратов базовой терапии, применявшихся для лечения сопутствующих заболеваний в период, предшествующий инфицированию, на риск летального исхода при новой коронавирусной инфекции. Данные международного регистра «Анализ динамики коморбидных заболеваний у пациентов, перенесших инфицирование SARS-CoV-2» (AКТИВ SARS-CoV-2) // Кардиология. ‒ 2021. – Т. 61, № 9. – С. 20-32. DOI:10.18087/cardio.2021.9.n1680.; Визель А., Визель И., Гизатуллина Э. Пневмония у больных ХОБЛ, получающих ингаляционные глюкокортикостероиды // Врач. ‒ 2017. ‒ № 1. – С. 17-23.; Визель А. А., Яушев М. Ф., Халфиев И. Н. Применение ингаляционного стероида ингакорта в комплексной терапии инфильтративного туберкулеза легких // Пульмонология. ‒ 2000. ‒ № 1. – С. 31-34.; Временные методические рекомендации. Профилактика, диагностика и лечение новой коронавирусной инфекции (2019-nCoV). Версия 13.1 (09.11.2021): 209-2010.; Гудима Г. О., Хаитов Р. М., Кудлай Д. А., Хаитов М. Р. Молекулярно-иммунологические аспекты диагностики, профилактики и лечения коронавирусной инфекции // Иммунология. ‒ 2021. ‒ Т. 42, № 3. ‒ С. 198-210. DOI: https://doi.org/10.33029/0206-4952-2021-42-3-198-210.; Фомина Д. С., Сердотецкова С. А., Иванова М. С., Белевский А. С., Княжеская Н. П., Лунцов А. В., Чернов А. А. Ведение пациентов с COVID-19 и бронхиальной астмой: обзор литературы и клинический опыт авторов // Практическая пульмонология. ‒ 2020. ‒ № 2. – С. 3-15.; Шпаков О. А. Ангиотензин-превращающий фермент 2-го типа как молекулярный посредник для инфицирования клетки вирусами SARS-CoV и SARS-CoV-2 // Российский физиологический журнал им. И. М. Сеченова. – 2020. – Т. 106, № 7. ‒ С. 795-810.; Agusti A., Torres F., Faner R. Early treatment with inhaled budesonide to prevent clinical deterioration in patients with COVID-19 // Lancet Respir Med. – 2021. – Vol. 9, № 7. ‒ P. 682-683. doi:10.1016/S2213-2600(21)00171-5.; Al Sulaiman K., Aljuhani O., Al Aamer K., Al Shaya O., Al Shaya A., Alsaeedi A. S, Alhubaishi A., Altebainawi A. F., Al Harthi A., Albelwi S., Almutairi R., Alsubaie N., Alsallum A., Korayem G. B., Alfahed A., Kensara R., Altebainawi E. F., Alenezi R. S., Alsulaiman T., Al Enazi H., Vishwakarma R., Al Dabbagh T., Bakhsh U., Al Ghamdi G. The Role of inhaled corticosteroids (ICS) in critically ill patients with COVID-19: A multicenter, cohort study // J. Intens. Care Med. – 2021. ‒ Nov 10:8850666211053548. doi:10.1177/08850666211053548.; Butler C. C., Yu L. M., Dorward J., Gbinigie O., Hayward G., Saville B. R., Van Hecke O., Berry N., Detry M. A., Saunders C., Fitzgerald M., Harris V., Djukanovic R., Gadola S., Kirkpatrick J., de Lusignan S., Ogburn E., Evans P. H., Thomas N. P. B., Patel M. G., Hobbs F. D. R. PRINCIPLE Trial Collaborative Group. Doxycycline for community treatment of suspected COVID-19 in people at high risk of adverse outcomes in the UK (PRINCIPLE): a randomised, controlled, open-label, adaptive platform trial // Lancet Respir. Med. – 2021. ‒ Vol. 9, № 9. – P. 1010-1020. doi:10.1016/S2213-2600(21)00310-6.; Choi J. C., Jung S. Y., Yoon U. A., You S. H., Kim M. S., Baek M. S., Jung J. W., Kim W. Y. Inhaled corticosteroids and COVID-19 risk and mortality: A Nationwide Cohort Study // J. Clin. Med. – 2020. – Vol. 9, № 11. – P. 3406. doi:10.3390/jcm9113406.; Clemency B. M., Varughese R., Gonzalez-Rojas Y., Morse C. G., Phipatanakul W., Koster D. J., Blaiss M. S. Efficacy of inhaled ciclesonide for outpatient treatment of adolescents and adults with symptomatic COVID-19: A Randomized Clinical Trial // JAMA Intern. Med. ‒ 2021 Nov 22. doi:10.1001/jamainternmed.2021.6759. Epub ahead of print.; Daval M., Corré A., Palpacuer C., Housset J., Poillon G., Eliezer M., Verillaud B., Slama D., Ayache D., Herman P., Jourdaine C., Hervé C., El Bakkouri W., Salmon D., Hautefort C. Efficacy of local budesonide therapy in the management of persistent hyposmia in COVID-19 patients without signs of severity: A structured summary of a study protocol for a randomised controlled trial // Trials. – 2020. – Vol. 21, № 1. – P. 666. doi:10.1186/s13063-020-04585-8.; Ebell M. H. Inhaled budesonide reduces the risk of emergency department evaluation or hospitalization in early COVID-19 // Am. Fam. Physician. – 2021. – Vol. 104, № 2. – P. 207-208. PMID: 34383442.; Efe C., Lammert C., Taşçılar K., Dhanasekaran R., Ebik B., Higuera-de la Tijera F., Calışkan A. R., Peralta M., Gerussi A., Massoumi H., Catana A. M., Purnak T., Rigamonti C., Gomez Aldana A. J., Khakoo N., Nazal L., Frager S., Demir N., Irak K., Melekoğlu Ellik Z., Kacmaz H., Balaban Y., Atay K., Eren F., Alvares-da-Silva M. R., Cristoferi L., Urzua Á., Eşkazan T., Magro B., Snijders R., Barutçu S., Lytvyak E., Miranda Zazueta G., Demirezer Bolat A., Aydın M., Heurgue-Berlot A., De Martin E., Ekin N., Yıldırım S., Yavuz A., Bıyık M., Castro Narro G., Kıyıcı M., Akyıldız M., Kahramanoğlu-Aksoy E., Vincent M., Carr R. M., Günşar F., Cerda Reyes E., Harputoğlu M., Aloman C., Gatselis N. K., Üstündağ Y., Brahm J., Chris Escajadillo Vargas N., Güzelbulut F., Ruiz Garcia S., Aguirre J., Anders M., Ratusnu N., Hatemi I., Mendizabal M., Floreani A., Fagiuoli S., Silva M., Idilman R., Satapathy S. K., Silveira M., Drenth J. P. H., Dalekos G. N., Assis D. N., Björnsson E., Boyer J. L., Yoshida E. M., Invernizzi P., Levy C., Montano-Loza A. J., Schiano T. D., Ridruejo E., Wahlin S. Effects of immunosuppressive drugs on COVID-19 severity in patients with autoimmune hepatitis // Liver Int. ‒ 2021. ‒ Nov 30. doi:10.1111/liv.15121. Epub ahead of print.; Farne H., Singanayagam A. Reply // J. Allergy Clin. Immunol. – 2021. – Vol. 147, № 3. – P. 1117-1118. doi:10.1016/j.jaci.2020.11.019.; Finney L. J., Glanville N., Farne H., Aniscenko J., Fenwick P., Kemp S. V., Trujillo-Torralbo M. B., Loo S. L., Calderazzo M. A., Wedzicha J. A., Mallia P., Bartlett N. W., Johnston S. L., Singanayagam A. Inhaled corticosteroids downregulate the SARS-CoV-2 receptor ACE2 in COPD through suppression of type I interferon // J. Allergy Clin. Immunol. – 2021. – Vol. 147, № 2. – P. 510-519.e5. doi:10.1016/j.jaci.2020.09.034. Epub 2020 Oct 15. PMID: 33068560; PMCID: PMC7558236.; Global Initiative for Asthma. Global Strategy for Asthma Management and Prevention, 2021. Availaible from: www.ginasthma.org (Accessed: December, 2021).; Global Initiative for Chronic Obstructive Lung Disease. Global Strategy for Prevention, Diagnosis and Management of COPD. 2022 GOLD Reports. Available at: https://goldcopd.org/gold-reports/ (Accessed: December, 2021).; Halpin D. M. G., Singh D., Hadfield R. M. Inhaled corticosteroids and COVID-19: a systematic review and clinical perspective // Eur. Respir. J. – 2020. – Vol. 55 (2001009). doi:10.1183/13993003.01009-2020.; Heinen N., Meister T. L., Klöhn M., Steinmann E., Todt D., Pfaender S. Antiviral effect of budesonide against SARS-CoV-2 // Viruses. – 2021. – Vol. 13, № 7. – P. 1411. doi:10.3390/v13071411.; Husby A., Pottegård A., Hviid A. Association between inhaled corticosteroid use and COVID-19 outcomes // Pharmacoepidemiol. Drug Saf. – 2021. – Vol. 30, № 11. – P. 1486-1492. doi:10.1002/pds.5345.; Iwabuchi K., Yoshie K., Kurakami Y., Takahashi K., Kato Y., Morishima T. Therapeutic potential of ciclesonide inahalation for COVID-19 pneumonia: Report of three cases // J. Infect. Chemother. – 2020. – Vol. 26, № 6. – P. 625-632. doi:10.1016/j.jiac.2020.04.007.; Jang J. G., Ahn J. H., Jin H. J. Incidence and prognostic factors of respiratory viral infections in severe acute exacerbation of chronic obstructive pulmonary disease // Int. J. Chron. Obstruct. Pulmon. Dis. – 2021. Vol. 7, № 16. – P. 1265-1273. doi:10.2147/COPD.S306916.; Jordan A., Sivapalan P., Jensen J. U. Does inhaled corticosteroid use affect the risk of COVID-19-related death? // Breathe (Sheff). ‒ 2021. – Vol. 17, № 1. – P. 200275. doi:10.1183/20734735.0275-2020.; Karampela I., Vallianou N. G., Tsilingiris D., Christodoulatos G. S., Muscogiuri G., Barrea L., Vitale G., Dalamaga M. Could inhaled corticosteroids be the game changers in the prevention of severe COVID-19? A review of current evidence // Panminerva Med. – 2021. ‒ Dec 3. doi:10.23736/S0031-0808.21.04595-X. Epub ahead of print.; Kareemi H., Rosenberg H., Yadav K. Is inhaled budesonide an effective treatment for patients with mild early symptoms of COVID-19? // CJEM. – 2021. – Vol. 23, № 5. ‒ P. 611-612. doi:10.1007/s43678-021-00154-3.; Kluge S., Nitschmann S., Scherer M. Inhalatives budesonid zur therapie bei COVID-19 [Inhaled budesonide in the treatment of COVID-19] // Internist (Berl). – 2021. ‒ Vol. 62, № 8. – P. 887-889. German. doi:10.1007/s00108-021-01071-4.; Lee S. C., Son K. J., Han C. H., Jung J. Y., Park S. C. Association between inhaled corticosteroid use and SARS-CoV-2 infection: A nationwide population-based study in South Korea // Tuberc. Respir. Dis. (Seoul). ‒ 2021. ‒ Nov 30. doi:10.4046/trd.2021.0102. Epub ahead of print.; Lipworth B., Chan R., Kuo C. Inhaled corticosteroids and angiotensinconverting enzyme-2 in COPD // J. Allergy Clin. Immunol. ‒ 2021. – Vol. 147, № 3. – P. 1117-1118. doi:10.1016/j.jaci.2020.11.019.; Mahase E. COVID-19: Increased demand for steroid inhalers causes "distressing" shortages. // BMJ. ‒ 2020. ‒ № 369. – P.m1393. doi:10.1136/bmj.m1393.; Milne S., Li X., Yang C. X., Leitao Filho F. S., Hernández Cordero A. I., Yang C. W. T., Shaipanich T., van Eeden S. F., Leung J. M., Lam S., Sin D. D. Inhaled corticosteroids downregulate SARS-CoV-2-related genes in COPD: № 1. – P. 2100130. doi:10.1183/13993003.00130-2021.; Nicolau D. V., Bafadhel M. Inhaled corticosteroids in virus pandemics: a treatment for COVID-19? // Lancet Respir. Med. ‒ 2020. – Vol. 8, № 9. – P. 846-847. doi:10.1016/S2213-2600(20)30314-3.; Patel S. K., Kumar R., Rana J., Agrawal A., Singh A., Kumar A. Budesonide: A promising candidate therapeutic for early COVID-19 // Ann. Med. Surg. (Lond). – 2021. ‒ № 68. – P. 102605. doi:10.1016/j.amsu.2021.102605.; Peters M. C., Sajuthi S., Deford P., Christenson S., Rios C. L., Montgomery M. T., Woodruff P. G., Mauger D. T., Erzurum S. C., Johansson M. W., Denlinger L. C., Jarjour N. N., Castro M., Hastie A. T., Moore W., Ortega V. E., Bleecker E. R., Wenzel S. E., Israel E., Levy B. D., Seibold M. A., Fahy J. V. COVID-19-related genes in sputum cells in asthma. Relationship to demographic features and corticosteroids // Am. J. Respir. Crit. Care Med. – 2020. – Vol. 202, № 1. – P. 83-90. doi:10.1164/rccm.202003-0821OC.; PRINCIPLE Trial Collaborative Group. Azithromycin for community treatment of suspected COVID-19 in people at increased risk of an adverse clinical course in the UK (PRINCIPLE): a randomised, controlled, open-label, adaptive platform trial // Lancet. 2021. ‒ Mar 20. ‒ № 397 (10279). ‒ Р. 1063-1074. doi:10.1016/S0140-6736(21)00461-X.; Ramakrishnan S., Nicolau D. V. Jr., Langford B., Mahdi M., Jeffers H., Mwasuku C., Krassowska K., Fox R., Binnian I., Glover V., Bright S., Butler C., Cane J. L., Halner A., Matthews P. C., Donnelly L. E., Simpson J. L., Baker J. R., Fadai N. T., Peterson S., Bengtsson T., Barnes P. J., Russell R. E. K., Bafadhel M. Inhaled budesonide in the treatment of early COVID-19 (STOIC): a phase 2, open-label, randomised controlled trial // Lancet Respir. Med. – 2021. – Vol. 9, № 7. – P. 763-772. doi:10.1016/S2213-2600(21)00160-0.; Rathi S., Ish P., Kalantri A., Kalantri S. Inhaled budesonide for mild COVID-19. Is there more to it than just airways? // Adv. Respir. Med. – 2021. – Vol. 89, № 5. – P. 552-553. doi:10.5603/ARM.a2021.0082.; RECOVERY Collaborative Group, Horby P., Lim W. S., Emberson J. R., Mafham M., Bell J. L., Linsell L., Staplin N., Brightling C., Ustianowski A., Elmahi E., Prudon B., Green C., Felton T., Chadwick D., Rege K., Fegan C., Chappell L. C., Faust S. N., Jaki T., Jeffery K., Montgomery A., Rowan K., Juszczak E., Baillie J. K., Haynes R., Landray M. J. Dexamethasone in hospitalized patients with COVID-19 // N. Engl. J. Med. – 2021. ‒ Vol. 25, № 384 (8). ‒ P. 693-704. doi:10.1056/NEJMoa2021436.; San-Juan R., Fernández-Ruiz M., López-Medrano F., Aguado J. M. Inhaled budesonide for early treatment of COVID-19 // Lancet Respir. Med. – 2021. – Vol. 9, № 7. – P. e58. doi:10.1016/S2213-2600(21)00211-3.; Schultze A., Walker A. J., MacKenna B., Morton C. E., Bhaskaran K., Brown J. P., Rentsch C. T., Williamson E., Drysdale H., Croker R., Bacon S., Hulme W., Bates C., Curtis H. J., Mehrkar A., Evans D., Inglesby P., Cockburn J., McDonald H. I., Tomlinson L., Mathur R., Wing K., Wong A. Y. S., Forbes H., Parry J., Hester F., Harper S., Evans S. J. W., Quint J., Smeeth L., Douglas I. J., Goldacre B. OpenSAFELY Collaborative. Risk of COVID-19-related death among patients with chronic obstructive pulmonary disease or asthma prescribed inhaled corticosteroids: an observational cohort study using the OpenSAFELY platform // Lancet Respir. Med. – 2020. – Vol. 8, № 11. – P. 1106-1120. doi:10.1016/S2213-2600(20)30415-X.; Schultze A., Walker A. J., MacKenna B., Morton C. E., Bhaskaran K., Brown J. P., Rentsch C. T., Williamson E., Drysdale H., Croker R., Bacon S., Hulme W., Bates C., Curtis H. J., Mehrkar A., Evans D., Inglesby P., Cockburn J., McDonald H. I., Tomlinson L., Mathur R., Wing K., Wong A. Y. S., Forbes H., Parry J., Hester F., Harper S., Evans S. J. W., Quint J., Smeeth L., Douglas I. J., Goldacre B. OpenSAFELY Collaborative. Inhaled corticosteroid use and risk COVID-19 related death among 966,461 patients with COPD or asthma: an OpenSAFELY analysis // MedRxiv. ‒ 2020; published online June 20. https://www.medrxiv.org/content/10.1101/2020.06.19.20135491v1 (preprint).; Sen P., Majumdar U., Zein J., Hatipoğlu U., Attaway A. H. Inhaled corticosteroids do not adversely impact outcomes in COVID-19 positive patients with COPD: An analysis of Cleveland Clinic's COVID-19 registry // PLoS One. – 2021. – Vol. 16, № 6. – P. e0252576. doi:10.1371/journal.pone.0252576.; Starshinova A., Malkova A., Yablonskiy P., Shoenfeld Y., Zinchenko U., Dovgalyk I., Kudlay D., Glushkova A. Efficacy of different types of therapy for COVID-19: a comprehensive review // Life. ‒2021. ‒ Vol. 11, № 8. ‒ Р. 753.; Wark P. A. B., Pathinayake P. S., Eapen M. S., Sohal S. S. Asthma, COPD and SARS-CoV-2 infection (COVID-19): potential mechanistic insights // Eur. Respir. J. 2021. – Vol. 58, № 2. – P. 100920. doi:10.1183/13993003.00920-2021.; Xiong R., Zhao Z., Lu H., Ma Y., Zeng H., Chen Y. Asthma patients benefit more than chronic obstructive pulmonary disease patients in the coronavirus disease 2019 рandemic // Front. Med (Lausanne). ‒ 2021. ‒ № 8. – P. 709006. doi:10.3389/fmed.2021.709006.; Yamaya M., Nishimura H., Deng X., Sugawara M., Watanabe O., Nomura K., Shimotai Y., Momma H., Ichinose M., Kawase T. Inhibitory effects of glycopyrronium, formoterol, and budesonide on coronavirus HCoV-229E replication and cytokine production by primary cultures of human nasal and tracheal epithelial cells // Respir. Investig. – 2020. – Vol. 58, № 3. – P. 155-168. doi:10.1016/j.resinv.2019.12.005.; Yu L. M., Bafadhel M., Dorward J., Hayward G., Saville B. R., Gbinigie O., Van Hecke O., Ogburn E., Evans P. H., Thomas N. P. B., Patel M. G., Richards D., Berry N., Detry M. A., Saunders C., Fitzgerald M., Harris V., Shanyinde M., de Lusignan S., Andersson M. I., Barnes P. J., Russell R. E. K., Nicolau D. V. Jr., Ramakrishnan S., Hobbs F. D. R., Butler C. C. PRINCIPLE Trial Collaborative Group. Inhaled budesonide for COVID-19 in people at high risk of complications in the community in the UK (PRINCIPLE): a randomised, controlled, open-label, adaptive platform trial // Lancet. – 2021. – Vol. 398, № 10303. – P. 843-855. doi:10.1016/S0140-6736(21)01744-X.