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    المساهمون: The article was prepared with the financial support of Solopharm, Статья подготовлена при финансовой поддержке компании Solopharm

    المصدر: PULMONOLOGIYA; Том 34, № 2 (2024); 158-174 ; Пульмонология; Том 34, № 2 (2024); 158-174 ; 2541-9617 ; 0869-0189

    وصف الملف: application/pdf

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A comparative study of polymicrobial diversity in CF and non-CF bronchiectasis. Thorax. 2010; 65 (4): A13–A14. DOI:10.1136/thx.2010.150912.23.; Foweraker J.E., Wat D. Microbiology of non-CF bronchiectasis. In: Floto R.A., Haworth C.S., eds. Bronchiectasis (out of print). Sheffield: ERS; 2011. Vol. 52: 68–96. DOI:10.1183/1025448x.10003610.; Finch S., McDonnell M.J., Abo-Leyah H. et al. A Comprehensive analysis of the impact of pseudomonas aeruginosa colonization on prognosis in adult bronchiectasis. Ann. Am. Thorac. Soc. 2015; 12 (11): 1602–1611. DOI:10.1513/AnnalsATS.201506-333OC.; Pasteur M.C., Helliwell S.M., Houghton S.J. et al. An investigation into causative factors in patients with bronchiectasis. Am. J. Respir. Crit. Care Med. 2000; 162 (4, Pt 1): 1277–1284. DOI:10.1164/ajrccm.162.4.9906120.; Reid L.M. Reduction in bronchial subdivision in bronchiectasis. Thorax. 1950; 5 (3): 233–247. DOI:10.1136/thx.5.3.233.; Angrill J., Agusti C., De Celis R. et al. Bronchial inflammation and colonization in patients with clinically stable bronchiectasis. Am. J. Respir. Crit. Care Med. 2001; 164 (9): 1628–1632. DOI:10.1164/ajrccm.164.9.2105083.; Chang A.B., Masel J.P., Boyce N.C. et al. Non-CF bronchiectasis: clinical and HRCT evaluation. Pediatr. Pulmonol. 2003; 35 (6): 477–483. DOI:10.1002/ppul.10289.; Remy Jardin M., Amara A., Campistron P. et al. Diagnosis of bronchiectasis with multislice spiral CT: accuracy of 3-mm-thick structured sections. Eur. Radiol. 2003; 13 (5): 1165–1171. DOI:10.1007/s00330-003-1821-z.; Naidich D.P., McCauley D.I., Khouri N.F. et al. Computed tomography of bronchiectasis. J. Comput. Assist. Tomogr. 1982; 6 (3): 437–444. DOI:10.1097/00004728-198206000-00001.; Hill T.A., Sullivan L.A., Chalmers D.J. et al. British Thoracic Society Guideline for bronchiectasis in adults. Thorax. 2019; 74 (Suppl. 1): 1–69. DOI:10.1136/thoraxjnl-2018-212463.; UpToDate. Barker A.F. 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DOI:10.1016/j.rmed.2011.07.019.; Herrero-Cortina B., Alcaraz V., Vilaro J. et al. Impact of hypertonic saline solutions on sputum expectoration and their safety profile in patients with bronchiectasis: a randomized crossover trial. J. Aerosol Med. Pulm. Drug Deliv. 2018; 31 (5): 281–289. DOI:10.1089/jamp.2017.1443.; Daviskas E., Anderson S.D., Gonda I. et al. Inhalation of hypertonic saline aerosol enhances mucociliary clearance in asthmatic and healthy subjects. Eur. Respir. J. 1996; 9 (4): 725–732. DOI:10.1183/09031936.96.09040725.; Elkins M.R., Robinson M., Rose B.R. et al. A controlled trial of longterm inhaled hypertonic saline in patients with cystic fibrosis. N. Engl. J. Med. 2006; 354 (3): 229–240. DOI:10.1056/NEJMoa043900.; Wark P., McDonald V.M. Nebulised hypertonic saline for cystic fibrosis. Cochrane Database Syst Rev. 2018; (9): CD001506. DOI:10.1002/14651858.CD001506.pub4.; Michon A.L., Jumas-Bilak E., Chiron R. et al. Advances toward the elucidation of hypertonic saline effects on Pseudomonas aeruginosa from cystic fibrosis patients. PLoS One. 2014; 9 (2): e90164. DOI:10.1371/journal.pone.0090164.; Garantziotis S., Brezina M., Castelnuovo P., Drago L. The role of hyaluronan in the pathobiology and treatment of respiratory disease. Am. J. Physiol. Lung Cell Mol. Physiol. 2016; 310 (9): L785–795. DOI:10.1152/ajplung.00168.2015.; Qi Q., Ailiyaer Y., Liu R. et al. Effect of N-acetylcysteine on exacerbations of bronchiectasis (BENE): a randomized controlled trial. Respir. Res. 2019; 20 (1): 73. DOI:10.1186/s12931-019-1042-x.; Hart A., Sugumar K., Milan S.J. et al. Inhaled hyperosmolar agents for bronchiectasis. Cochrane Database Syst. Rev. 2014; (5): CD002996. DOI:10.1002/14651858.CD002996.pub3.; Wilkinson M., Sugumar K., Milan S.J. et al. Mucolytics for bronchiectasis. Cochrane Database Syst. Rev. 2014 (5): CD001289. DOI:10.1002/14651858.CD001289.pub2.; Wills P., Greenstone M. Inhaled hyperosmolar agents for bronchiectasis. Cochrane Database Syst. Rev. 2002; (1): CD002996. DOI:10.1002/14651858.cd002996.; Redding G.J. Bronchiectasis in children. Pediatr. Clin. North Am. 2009; 56 (1): 157–171. DOI:10.1016/j.pcl.2008.10.014.; Chalmers J.D., Polverino E., Crichton M.L. et al. Bronchiectasis in Europe: data on disease characteristics from the European Bronchiectasis registry (EMBARC). Lancet Respir. Med. 2023; 11 (7): 637–649. DOI:10.1016/S2213-2600(23)00093-0.; Jayaram L., King P.T., Hunt J. et al. Evaluation of high dose N-acetylcysteine on airway inflammation and quality of life outcomes in adults with bronchiectasis: a randomised placebo-controlled pilot study. Pulm. Pharmacol. Ther. 2023; 84: 102283. DOI:10.1016/j.pupt.2023.102283.; Minov J., Stoleski S., Petrova T. et al. Effects of a long-term use of carbocysteine on frequency and duration of exacerbations in patients with bronchiectasis. Open Access Maced. J. Med. Sci. 2019; 7 (23): 4030–4035. DOI:10.3889/oamjms.2019.697.; Liao Y., Wu Y., Zi K. et al. The effect of N-acetylcysteine in patients with non-cystic fibrosis bronchiectasis (NINCFB): study protocol for a multicentre, double-blind, randomised, placebo-controlled trial. BMC Pulm. Med. 2022; 22 (1): 401. DOI:10.1186/s12890-022-02202-9.; Bradley J.M., Anand R., O’Neill B. et al. A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial. Trials. 2019; 20 (1): 747. DOI:10.1186/s13063-019-3766-9.; Chang A.B., Morgan L.C., Duncan E.L. et al. Reducing exacerbations in children and adults with primary ciliary dyskinesia using erdosteine and/or azithromycin therapy (REPEAT trial): study protocol for a multicentre, double-blind, double-dummy, 2×2 partial factorial, randomised controlled trial. BMJ Open Respir. Res. 2022; 9 (1): e001236. DOI:10.1136/bmjresp-2022-001236.; Serra A., Schito G.C., Nicoletti G., Fadda G. A therapeutic approach in the treatment of infections of the upper airways: thiamphenicol glycinate acetylcysteinate in sequential treatment (systemic-inhalatory route). Int. J. Immunopathol. Pharmacol. 2007; 20 (3): 607–617. DOI:10.1177/039463200702000319.; Blasi F., Page C., Rossolini G.M. et al. The effect of N-acetylcysteine on biofilms: Implications for the treatment of respiratory tract infections. Respir Med. 2016; 117: 190–197. DOI:10.1016/j.rmed.2016.06.015.; Olofsson A.C., Hermansson M., Elwing H. N-acetyl-L-cysteine affects growth, extracellular polysaccharide production, and bacterial biofilm formation on solid surfaces. Appl. Environ. Microbiol. 2003; 69 (8): 4814–4822. DOI:10.1128/aem.69.8.4814-4822.2003.; Иванчик Н.В., Сухорукова М.В., Чагарян А.Н. и др. In vitro активность тиамфеникола в отношении клинических изолятов Haemophilus influenzae, Streptococcus pneumoniae и Streptococcus pyogenes. Клиническая микробиология и антимикробная химиотерапия. 2021; 23 (1): 92–99. DOI:10.36488/cmac.2021.1.92-99.; Bilton D., Tino G., Barker A.F. et al. Inhaled mannitol for non-cystic fibrosis bronchiectasis: a randomised, controlled trial. Thorax. 2014; 69 (12): 1073–1079. DOI:10.1136/thoraxjnl-2014-205587.; Lee A.L., Gordon C.S., Osadnik C.R. Exercise training for bronchiectasis. Cochrane Database Syst. Rev. 2021; 4 (4): CD013110. DOI:10.1002/14651858.cd013110.pub2.; Etienne T., Spiliopoulos A., Megevand R. [Bronchiectasis: indication and timing for surgery]. Ann. Chir. 1993; 47 (8): 729–735 (in French).; Yu J.A., Pomerantz M., Bishop A. et al. Lady windermere revisited: treatment with thoracoscopic lobectomy/segmentectomy for right middle lobe and lingular bronchiectasis associated with non-tuberculous mycobacterial disease. Eur. J. Cardiothorac. Surg. 2011; 40 (3): 671–675. DOI:10.1016/j.ejcts.2010.12.028.; Weill D., Benden C., Corris P.A. et al. A consensus document for the selection of lung transplant candidates: 2014 – an update from the Pulmonary Transplantation Council of the International Society for Heart and Lung Transplantation. J. Heart Lung Transplant. 2015; 34 (1): 1–15. DOI:10.1016/j.healun.2014.06.014.; Fujimoto T., Hillejan L., Stamatis G. Current strategy for surgical management of bronchiectasis. Ann. Thorac Surg. 2001; 72 (5): 1711–1715. DOI:10.1016/s0003-4975(01)03085-5.; Kutlay H., Cangir A.K., Enon S. et al. Surgical treatment in bronchiectasis: analysis of 166 patients. Eur. J. Cardiothorac. Surg. 2002; 21 (4): 634–637. DOI:10.1016/s1010-7940(02)00053-2.; Leard L.E., Holm A.M., Valapour M. et al. Consensus document for the selection of lung transplant candidates: An update from the International Society for heart and lung transplantation. J. Heart Lung Transplant. 2021; 40 (11): 1349–1379. DOI:10.1016/j.healun.2021.07.005.; https://journal.pulmonology.ru/pulm/article/view/4474

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    المساهمون: The study was conducted with the support of Zambon Pharma, Исследование проведено при поддержке компании Zambon Pharma

    المصدر: PULMONOLOGIYA; Том 34, № 1 (2024); 105-113 ; Пульмонология; Том 34, № 1 (2024); 105-113 ; 2541-9617 ; 0869-0189

    وصف الملف: application/pdf

    Relation: https://journal.pulmonology.ru/pulm/article/view/4463/3605; Клячкина И.Л. Все ли мы знаем об ацетилцистеине? Фарматека. 2021; 28 (10): 103–110. DOI:10.18565/pharmateca.2021.10.103-110.; Samuni Y., Goldstein S., Dean O.M., Berk M. The chemistry and biological activities of N-acetylcysteine. Biochim. Biophys. Acta. 2013; 1830 (8): 4117–4129. DOI:10.1016/j.bbagen.2013.04.016.; Izquierdo-Alonso J.L., Pérez-Rial S., Rivera C.G., Peces-Barba G. N-acetylcysteine for prevention and treatment of COVID-19: current state of evidence and future directions. J. Infect. Public Health. 2022; 15 (12): 1477–1483. DOI:10.1016/j.jiph.2022.11.009.; Avdeev S.N., Gaynitdinova V.V., Merzhoeva Z.M., Berikkhanov Z.G. N-acetylcysteine for the treatment of COVID-19 among hospitalized patients. J. Infect. 2022; 84 (1): 94–118. DOI:10.1016/j.jinf.2021.07.003.; Mokra D., Mokry J., Barosova R., Hanusrichterova J. Advances in the use of N-acetylcysteine in chronic respiratory diseases. Antioxidants (Basel). 2023, 12 (9): 1713. DOI:10.3390/antiox12091713.; Cazzola M., Calzetta L., Page C. et al. Influence of N-acetylcysteine on chronic bronchitis or COPD exacerbations: a meta-analysis. Eur. Respir. Rev. 2015; 24 (137): 451–461. DOI:10.1183/16000617.00002215.; Grandjean E.M., Berthet P., Ruffmann R., Leuenberger P. Efficacy of oral long-term N-acetylcysteine in chronic bronchopulmonary disease: a meta-analysis of published double-blind, placebo-controlled clinical trials. Clin. Ther. 2000; 22 (2): 209–221. DOI:10.1016/S0149-2918(00)88479-9.; Stey C., Steurer J., Bachmann S. et al. The effect of oral N-acetylcysteine in chronic bronchitis: a quantitative systematic review. Eur. Respir. J. 2000; 16 (2): 253–262. DOI:10.1034/j.1399-3003.2000.16b12.x.; Hansen N.C., Skriver A., Brorsen-Riis L. et al. Orally administered N-acetylcysteine may improve general well-being in patients with mild chronic bronchitis. Respir. Med. 1994; 88 (7): 531–535. 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