Highlights & Basics
- Bronchiectasis often presents with recurrent pulmonary infections, including a chronic daily productive cough with mucopurulent sputum production.
- High-resolution chest computed tomography is the confirmatory test.
- Diagnostic testing is geared toward identifying the underlying etiology, as treatment will be successful only if it treats both the bronchiectasis and any underlying disease process.
- A sputum sample should be obtained when the patient is in a stable state and during acute exacerbations. Antibiotics are used in three scenarios: to treat acute exacerbations, eradication of a first or new isolation of Pseudomonas aeruginosa, and long-term antibiotics to suppress chronic bacterial infection. Where possible, antibiotic choice should be based on culture and sensitivity from sputum samples.
- Daily airway clearance is essential for treatment success.
Quick Reference
History & Exam
Key Factors
Other Factors
Diagnostics Tests
Treatment Options
Definition
Epidemiology
Etiology
Pathophysiology
Images
Mucus-impacted bronchi in a 36-year-old woman with allergic bronchopulmonary aspergillosis
Situs inversus (Kartagener syndrome) in a 19-year-old woman with focal bronchiectasis from primary ciliary dyskinesia
Chest x-ray with dilated and thickened airways
Chest x-ray with lack of normal tapering producing a tram line
Chest computed tomography scan with dilated and thickened airways and peripheral tree-in-bud pattern
Chest computed tomography scan with presence of signet ring on left
Signet ring signs in a 20-year-old woman with bronchiectasis
Severe cystic and varicose bronchiectasis in a 49-year-old man with idiopathic bronchiectasis and scoliosis
Citations
Chang AB, Fortescue R, Grimwood K, et al. European Respiratory Society guidelines for the management of children and adolescents with bronchiectasis. Eur Respir J. 2021 Aug;58(2):2002990.[Abstract][Full Text]
Hill AT, Sullivan AL, Chalmers JD, et al. British Thoracic Society guideline for bronchiectasis in adults. Thorax. 2019 Jan;74(suppl 1):1-69.[Abstract][Full Text]
Polverino E, Goeminne PC, McDonnell MJ, et al. European Respiratory Society guidelines for the management of adult bronchiectasis. Eur Respir J. 2017 Sep 9;50(3):1700629.[Abstract][Full Text]
O'Donnell AE. Bronchiectasis - a clinical review. N Engl J Med. 2022 Aug 11;387(6):533-45.[Abstract]
Hill AT, Barker AF, Bolser DC, et al. Treating cough due to non-CF and CF bronchiectasis with nonpharmacological airway clearance: CHEST Expert Panel Report. Chest. 2018 Apr;153(4):986-93.[Abstract][Full Text]
Smith D, Du Rand I, Addy CL, et al. British Thoracic Society guideline for the use of long-term macrolides in adults with respiratory disease. Thorax. 2020 May;75(5):370-404.[Abstract][Full Text]
1. Laennec RT. A treatise on the disease of the chest. Forbes J, trans. New York, NY: Macmillan (Hafner Press);1962:78.
2. Reid LM. Reduction in bronchial subdivision in bronchiectasis. Thorax. 1950 Sep;5(3):233-47.[Abstract][Full Text]
3. Rosen MJ. Chronic cough due to bronchiectasis: ACCP evidence-based clinical practice guidelines. Chest. 2006 Jan;129(1 suppl):122S-31S.[Abstract][Full Text]
4. Barker AF. Bronchiectasis. New Engl J Med. 2002 May 2;346(18):1383-93.[Abstract]
5. Liebow AA, Hales MR, Lindskog GE. Enlargement of the bronchial arteries, and their anastomoses with the pulmonary arteries in bronchiectasis. Am J Pathol. 1949 Mar;25(2):211-31.[Abstract][Full Text]
6. Weyker D, Edelsberg J, Oster G, et al. Prevalence and economic burden of bronchiectasis. Clin Pulm Med. 2005;12:205.
7. Seitz AE, Olivier KN, Adjemian J, et al. Trends in bronchiectasis among medicare beneficiaries in the United States, 2000 to 2007. Chest. 2012 Aug;142(2):432-39.[Abstract][Full Text]
8. Goeminne PC, Hernandez F, Diel R, et al. The economic burden of bronchiectasis - known and unknown: a systematic review. BMC Pulm Med. 2019 Feb 28;19(1):54.[Abstract][Full Text]
9. Chang AB, Fortescue R, Grimwood K, et al. European Respiratory Society guidelines for the management of children and adolescents with bronchiectasis. Eur Respir J. 2021 Aug;58(2):2002990.[Abstract][Full Text]
10. Twiss J, Metcalfe R, Edwards E, et al. New Zealand national incidence of bronchiectasis "too high" for a developed country. Arch Dis Child. 2005 Jul;90(7):737-40.[Abstract]
11. King PT, Holdsworth SR, Farmer M, et al. Phenotypes of adult bronchiectasis: onset of productive cough in childhood and adulthood. COPD. 2009 Apr;6(2):130-6.[Abstract][Full Text]
12. Araújo D, Shteinberg M, Aliberti S, et al. Standardised classification of the aetiology of bronchiectasis using an objective algorithm. Eur Respir J. 2017 Dec;50(6):1701289.[Abstract][Full Text]
13. Ojha V, Mani A, Pandey NN, et al. CT in coronavirus disease 2019 (COVID-19): a systematic review of chest CT findings in 4410 adult patients. Eur Radiol. 2020 Nov;30(11):6129-38.[Abstract][Full Text]
14. Fraser E. Long term respiratory complications of covid-19. BMJ. 2020 Aug 3;370:m3001.[Abstract][Full Text]
15. Gao YH, Guan WJ, Liu SX, et al. Aetiology of bronchiectasis in adults: a systematic literature review. Respirology. 2016 Nov;21(8):1376-83.[Abstract][Full Text]
16. Jamee M, Zaki-Dizaji M, Lo B, et al. Clinical, immunological, and genetic features in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-like syndrome. J Allergy Clin Immunol Pract. 2020 Sep;8(8):2747-60.[Abstract]
17. Mercuzot C, Letertre S, Daien CI, et al. Comorbidities and health-related quality of life in patients with antineutrophil cytoplasmic antibody (ANCA) - associated vasculitis. Autoimmun Rev. 2021 Jan;20(1):102708.[Abstract]
18. Schierhout G, McGregor S, Gessain A, et al. Association between HTLV-1 infection and adverse health outcomes: a systematic review and meta-analysis of epidemiological studies. Lancet Infect Dis. 2020 Jan;20(1):133-43.[Abstract]
19. Normando VMF PhD, Dias ÁRN Me, da Silva ALSE Lic, et al. HTLV-I induces lesions in the pulmonary system: a systematic review. Life Sci. 2020 Sep 1;256:117979.[Abstract]
20. Chang AB, Bush A, Grimwood K. Bronchiectasis in children: diagnosis and treatment. Lancet. 2018 Sep 8;392(10150):866-79.[Abstract]
21. Chang AB, Bilton D. Exacerbations in cystic fibrosis: 4 - non-cystic fibrosis bronchiectasis. Thorax. 2008 Mar;63(3):269-76.[Abstract][Full Text]
22. Gao YH, Guan WJ, Xu G, et al. The role of viral infection in pulmonary exacerbations of bronchiectasis in adults: a prospective study. Chest. 2015 Jun;147(6):1635-43.[Abstract][Full Text]
23. Cole PJ. Host microbe relationships in chronic respiratory infection. Respiration. 1989;55 (Suppl 1):5-8.[Abstract]
24. Morrissey BM. Pathogenesis of bronchiectasis. Clin Chest Med. 2007 Jun;28(2):289-96.[Abstract]
25. Burgel PR, Montani D, Danel C, et al. A morphometric study of mucins and small airway plugging in cystic fibrosis. Thorax. 2007 Feb;62(2):153-61.[Abstract][Full Text]
26. Rodman DM. Late diagnosis defines a unique population of long-term survivors of cystic fibrosis. Am J Resp Crit Care Med. 2005 Mar 15;171(6):621-6.[Abstract]
27. Rosen FS, Cooper MD, Wedgwood RJ. The primary immunodeficiencies. N Engl J Med. 1995 Aug 17;333(7):431-40.[Abstract]
28. Cunningham-Rundles C, Bodian C. Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol. 1999 Jul;92(1):34-48.[Abstract]
29. Hartl D, Latzin P, Zissel G, et al. Chemokines indicate allergic bronchopulmonary aspergillosis in patients with cystic fibrosis. Am J Respir Crit Care Med. 2006 Jun 15;173(12):1370-6.[Abstract][Full Text]
30. Prince DS, Peterson DD, Steiner RM, et al. Infection with Mycobacterium avium complex in patients without predisposing conditions. N Engl J Med. 1989 Sep 28;321(13):863-8.[Abstract]
31. Elborn JS. Cystic fibrosis. Lancet. 2016 Nov 19;388(10059):2519-31.[Abstract]
32. Lucas JS, Barbato A, Collins SA, et al. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia. Eur Respir J. 2017 Jan 4;49(1):1601090.[Abstract][Full Text]
33. Le Mauviel L. Primary ciliary dyskinesia. West J Med. 1991 Sep;155(3):280-3.[Abstract][Full Text]
34. Shapiro AJ, Davis SD, Polineni D, et al. Diagnosis of primary ciliary dyskinesia. An official American Thoracic Society clinical practice guideline. Am J Respir Crit Care Med. 2018 Jun 15;197(12):e24-e39.[Abstract][Full Text]
35. Knowles MR, Daniels LA, Davis SD, et al. Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease. Am J Respir Crit Care Med. 2013 Oct 15;188(8):913-22.[Abstract][Full Text]
36. Cuvelier A, Muir JF, Hellot MF, et al. Distribution of alpha(1)-antitrypsin alleles in patients with bronchiectasis. Chest. 2000 Feb;117(2):415-9.[Abstract][Full Text]
37. McMahon MJ, Swinson DR, Shettar S, et al. Bronchiectasis and rheumatoid arthritis: a clinical study. Ann Rheum Dis. 1993 Nov;52(11):776-9.[Abstract]
38. Camus P, Colby TV. The lung in inflammatory bowel disease. Eur Respir J. 2000 Jan;15(1):5-10.[Abstract][Full Text]
39. Silva JR, Jones JA, Cole PJ, et al. The immunological component of the cellular inflammatory infiltrate in bronchiectasis. Thorax. 1989 Aug;44(8):668-73.[Abstract][Full Text]
40. Kim RD, Greenberg DE, Ehrmantraut ME, et al. Pulmonary nontuberculous mycobacterial disease: prospective study of a distinct preexisting syndrome. Am J Respir Crit Care Med. 2008 Nov 15;178(10):1066-74.[Abstract][Full Text]
41. Singleton RJ, Valery PC, Morris P, et al. Indigenous children from three countries with non-cystic fibrosis chronic suppurative lung disease/bronchiectasis. Pediatr Pulmonol. 2014 Feb;49(2):189-200.[Abstract]
42. Pasteur MC, Helliwell SM, Houghton SJ, et al. An investigation into causative factors in patients with bronchiectasis. Am J Respir Crit Care Med. 2000 Oct;162(4 Pt 1):1277-84.[Abstract]
43. Hill AT, Sullivan AL, Chalmers JD, et al. British Thoracic Society guideline for bronchiectasis in adults. Thorax. 2019 Jan;74(suppl 1):1-69.[Abstract][Full Text]
44. Nicotra MB, Rivera M, Dale AM, et al. Clinical, pathophysiologic, and microbiologic characterization of bronchiectasis in an aging cohort. Chest. 1995 Oct;108(4):955-61.[Abstract][Full Text]
45. Handley E, Nicolson CH, Hew M, et al. Prevalence and clinical implications of chronic rhinosinusitis in people with bronchiectasis: a systematic review. J Allergy Clin Immunol Pract. 2019 Jul - Aug;7(6):2004-12.[Abstract]
46. Konstan MW, Morgan WJ, Butler SM, et al.; Scientific Advisory Group and the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J Pediatr. 2007 Aug;151(2):134-9.[Abstract]
47. Courtney JM, Bradley J, Mccaughan J, et al. Predictors of mortality in adults with cystic fibrosis. Pediatr Pulmonol. 2007 Jun;42(6):525-32.[Abstract]
48. Rivera M. Pseudomonas aeruginosa mucoid strain: its significance in adult chest diseases. Am Rev Respir Dis. 1982 Nov;126(5):833-6.[Abstract]
49. Moss RB. Fungi in cystic fibrosis and non-cystic fibrosis bronchiectasis. Semin Respir Crit Care Med. 2015 Apr;36(2):207-16.[Abstract]
50. Woodworth MH, Saullo JL, Lantos PM, et al. Increasing Nocardia incidence associated with bronchiectasis at a tertiary care center. Ann Am Thorac Soc. 2017 Mar;14(3):347-54.[Abstract][Full Text]
51. Farrell PM, White TB, Ren CL, et al. Diagnosis of cystic fibrosis: consensus guidelines from the Cystic Fibrosis Foundation. J Pediatr. 2017 Feb;181S:S4-S15.e1.[Abstract][Full Text]
52. Stoller JK, Aboussouan LS. Alpha1-antitrypsin deficiency. Lancet. 2005 Jun 25-Jul 1;365(9478):2225-36.[Abstract]
53. Paris K, Sorensen RU. Assessment and clinical interpretation of polysaccharide antibody responses. Ann Allergy Asthma Immunol. 2007 Nov;99(5):462-4.[Abstract]
54. Verghese A. Bacterial bronchitis and bronchiectasis in human immunodeficiency virus infection. Arch Intern Med. 1994 Sep 26;154(18):2086-91.[Abstract]
55. Shapiro AJ, Josephson M, Rosenfeld M, et al. Accuracy of nasal nitric oxide measurement as a diagnostic test for primary ciliary dyskinesia. A systematic review and meta-analysis. Ann Am Thorac Soc. 2017 Jul;14(7):1184-96.[Abstract][Full Text]
56. Chang AB, Oppenheimer JJ, Irwin RS, et al. Managing chronic cough as a symptom in children and management algorithms: CHEST guideline and expert panel report. Chest. 2020 Jul;158(1):303-29.[Abstract][Full Text]
57. Hansell DM. Bronchiectasis. Radiol Clin North Am. 1998 Jan;36(1):107-28.[Abstract]
58. Hansell DM. Imaging of diseases of the chest. 4th ed. Philadelphia, PA: Elsevier Mosby; 1995.
59. American College of Radiology. ACR appropriateness criteria: hemoptysis. 2019 [internet publication].[Full Text]
60. American College of Radiology. ACR appropriateness criteria: chronic dyspnea - noncardiovascular origin. 2018 [internet publication].[Full Text]
61. Polverino E, Goeminne PC, McDonnell MJ, et al. European Respiratory Society guidelines for the management of adult bronchiectasis. Eur Respir J. 2017 Sep 9;50(3):1700629.[Abstract][Full Text]
62. Chang AB, Bell SC, Torzillo PJ, et al. Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand Thoracic Society of Australia and New Zealand guidelines. Med J Aust. 2015 Jan 19;202(1):21-3.[Abstract][Full Text]
63. O'Donnell AE. Bronchiectasis - a clinical review. N Engl J Med. 2022 Aug 11;387(6):533-45.[Abstract]
64. Hill AT, Barker AF, Bolser DC, et al. Treating cough due to non-CF and CF bronchiectasis with nonpharmacological airway clearance: CHEST Expert Panel Report. Chest. 2018 Apr;153(4):986-93.[Abstract][Full Text]
65. Lee AL, Burge AT, Holland AE. Airway clearance techniques for bronchiectasis. Cochrane Database Syst Rev. 2015 Nov 23;(11):CD008351.[Abstract][Full Text]
66. Lee AL, Burge AT, Holland AE. Positive expiratory pressure therapy versus other airway clearance techniques for bronchiectasis. Cochrane Database Syst Rev. 2017 Sep 27;9:CD011699.[Abstract][Full Text]
67. Morrison L, Milroy S. Oscillating devices for airway clearance in people with cystic fibrosis. Cochrane Database Syst Rev. 2020 Apr 30;(4):CD006842.[Abstract][Full Text]
68. Muñoz G, de Gracia J, Buxó M, et al. Long-term benefits of airway clearance in bronchiectasis: a randomised placebo-controlled trial. Eur Respir J. 2018 Jan;51(1):1701926.[Abstract][Full Text]
69. Basavaraj A, Choate R, Addrizzo-Harris D, et al. Airway clearance techniques in bronchiectasis: analysis from the United States Bronchiectasis and Non-TB Mycobacteria Research Registry. Chest. 2020 Oct;158(4):1376-84.[Abstract][Full Text]
70. Chalmers JD, McHugh BJ, Docherty C, et al. Vitamin-D deficiency is associated with chronic bacterial colonisation and disease severity in bronchiectasis. Thorax. 2013 Jan;68(1):39-47.[Abstract][Full Text]
71. Onen ZP, Gulbay BE, Sen E, et al. Analysis of the factors related to mortality in patients with bronchiectasis. Respir Med. 2007 Jul;101(7):1390-7.[Abstract]
72. Lee AL, Gordon CS, Osadnik CR. Exercise training for bronchiectasis. Cochrane Database Syst Rev. 2021 Apr 6;4(4):CD013110.[Abstract][Full Text]
73. Lee AL, Hill CJ, McDonald CF, et al. Pulmonary rehabilitation in individuals with non-cystic fibrosis bronchiectasis: a systematic review. Arch Phys Med Rehabil. 2017 Apr;98(4):774-82.e1.[Abstract]
74. Cox NS, Dal Corso S, Hansen H, et al. Telerehabilitation for chronic respiratory disease. Cochrane Database Syst Rev. 2021 Jan 29;1(1):CD013040.[Abstract][Full Text]
75. Kelly C, Grundy S, Lynes D, et al. Self-management for bronchiectasis. Cochrane Database Syst Rev. 2018 Feb 7;2(2):CD012528.[Abstract][Full Text]
76. White L, Mirrani G, Grover M, et al. Outcomes of Pseudomonas eradication therapy in patients with non-cystic fibrosis bronchiectasis. Respir Med. 2012 Mar;106(3):356-60.[Abstract][Full Text]
77. Orriols R, Hernando R, Ferrer A, et al. Eradication therapy against Pseudomonas aeruginosa in non-cystic fibrosis bronchiectasis. Respiration. 2015;90(4):299-305.[Abstract][Full Text]
78. Hnin K, Nguyen C, Carson KV, et al. Prolonged antibiotics for non-cystic fibrosis bronchiectasis in children and adults. Cochrane Database Syst Rev. 2015 Aug 13;(8):CD001392.[Abstract][Full Text]
79. Abu Dabrh AM, Hill AT, Dobler CC, et al. Prevention of exacerbations in patients with stable non-cystic fibrosis bronchiectasis: a systematic review and meta-analysis of pharmacological and non-pharmacological therapies. BMJ Evid Based Med. 2018 Jun;23(3):96-103.[Abstract][Full Text]
80. Smith D, Du Rand I, Addy CL, et al. British Thoracic Society guideline for the use of long-term macrolides in adults with respiratory disease. Thorax. 2020 May;75(5):370-404.[Abstract][Full Text]
81. Kelly C, Chalmers JD, Crossingham I, et al. Macrolide antibiotics for bronchiectasis. Cochrane Database Syst Rev. 2018 Mar 15;3:CD012406.[Abstract][Full Text]
82. Goyal V, Grimwood K, Byrnes CA, et al. Amoxicillin-clavulanate versus azithromycin for respiratory exacerbations in children with bronchiectasis (BEST-2): a multicentre, double-blind, non-inferiority, randomised controlled trial. Lancet. 2018 Oct 6;392(10154):1197-206.[Abstract]
83. Chalmers JD, Boersma W, Lonergan M, et al. Long-term macrolide antibiotics for the treatment of bronchiectasis in adults: an individual participant data meta-analysis. Lancet Respir Med. 2019 Oct;7(10):845-54.[Abstract]
84. Choo JM, Abell GCJ, Thomson R, et al. Impact of long-term erythromycin therapy on the oropharyngeal microbiome and resistance gene reservoir in non-cystic fibrosis bronchiectasis. mSphere. 2018 Apr 18;3(2):e00103-18.[Abstract][Full Text]
85. Li W, Qin Z, Gao J, et al. Azithromycin or erythromycin? Macrolides for non-cystic fibrosis bronchiectasis in adults: a systematic review and adjusted indirect treatment comparison. Chron Respir Dis. 2019 Jan-Dec;16:1479972318790269.[Abstract][Full Text]
86. Spencer S, Donovan T, Chalmers JD, et al. Intermittent prophylactic antibiotics for bronchiectasis. Cochrane Database Syst Rev. 2022 Jan 5;1(1):CD013254.[Abstract][Full Text]
87. Chang KC, Leung CC, Yew WW, et al. Newer fluoroquinolones for treating respiratory infection: do they mask tuberculosis? Eur Respir J. 2010 Mar;35(3):606-13.[Abstract]
88. European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. Mar 2019 [internet publication].[Full Text]
89. US Food and Drug Administration. FDA drug safety communication. FDA warns about increased risk of ruptures or tears in the aorta blood vessel with fluoroquinolone antibiotics in certain patients. Dec 2018 [internet publication].[Full Text]
90. US Food and Drug Administration. FDA drug safety communication. FDA reinforces safety information about serious low blood sugar levels and mental health side effects with fluoroquinolone antibiotics; requires label changes. Jul 2018 [internet publication].[Full Text]
91. O'Donnell AE. Bronchiectasis: which antibiotics to use and when? Curr Opin Pulm Med. 2015 May;21(3):272-7.[Abstract]
92. Paredes Aller S, Quittner AL, Salathe MA, et al. Assessing effects of inhaled antibiotics in adults with non-cystic fibrosis bronchiectasis--experiences from recent clinical trials. Expert Rev Respir Med. 2018 Sep;12(9):769-82.[Abstract]
93. Laska IF, Crichton ML, Shoemark A, et al. The efficacy and safety of inhaled antibiotics for the treatment of bronchiectasis in adults: a systematic review and meta-analysis. Lancet Respir Med. 2019 Oct;7(10):855-69.[Abstract]
94. Nicolson CH, Stirling RG, Borg BM, et al. The long term effect of inhaled hypertonic saline 6% in non-cystic fibrosis bronchiectasis. Respir Med. 2012 May;106(5):661-7.[Abstract]
95. Reeves EP, Williamson M, O'Neill SJ, et al. Nebulized hypertonic saline decreases IL-8 in sputum of patients with cystic fibrosis. Am J Respir Crit Care Med. 2011 Jun 1;183(11):1517-23.[Abstract][Full Text]
96. Herrero-Cortina B, Alcaraz V, Vilaró 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 Oct;31(5):281-9.[Abstract][Full Text]
97. Bilton D, Daviskas E, Anderson SD, et al; B301 Investigators. Phase 3 randomized study of the efficacy and safety of inhaled dry powder mannitol for the symptomatic treatment of non-cystic fibrosis bronchiectasis. Chest. 2013 Jul;144(1):215-25.[Abstract]
98. Tarrant BJ, Le Maitre C, Romero L, et al. Mucoactive agents for chronic, non-cystic fibrosis lung disease: a systematic review and meta-analysis. Respirology. 2017 Aug;22(6):1084-92.[Abstract][Full Text]
99. Bilton D, Tino G, Barker AF, et al; B-305 Study Investigators. Inhaled mannitol for non-cystic fibrosis bronchiectasis: a randomised, controlled trial. Thorax. 2014 Dec;69(12):1073-9.[Abstract]
100. Hart A, Sugumar K, Milan SJ, et al. Inhaled hyperosmolar agents for bronchiectasis. Cochrane Database Syst Rev. 2014 May 12;(5):CD002996.[Abstract][Full Text]
101. Crasafulli E, Colettu O, Costi S, et al. Effectiveness of erdosteine in elderly patients with bronchiectasis and hypersecretion: a 15-day prospective, parallel, open- label, pilot study. Clin Ther. 2007 Sep;29(9):2001-9.[Abstract]
102. Wilkinson M, Sugumar K, Milan SJ, et al. Mucolytics for bronchiectasis. Cochrane Database Syst Rev. 2014 May 2;(5):CD001289.[Abstract][Full Text]
103. Qi Q, Ailiyaer Y, Liu R, et al. Effect of N-acetylcysteine on exacerbations of bronchiectasis (BENE): a randomized controlled trial. Respir Res. 2019 Apr 11;20(1):73.[Abstract][Full Text]
104. Tsang KW, Tan KC, Ho PL, et al. Inhaled fluticasone in bronchiectasis: a 12 month study. Thorax. 2005 Mar;60(3):239-43.[Abstract]
105. Kapur N, Petsky HL, Bell S, et al. Inhaled corticosteroids for bronchiectasis. Cochrane Database Syst Rev. 2018 May 16;5:CD000996.[Abstract][Full Text]
106. Brode SK, Campitelli MA, Kwong JC, et al. The risk of mycobacterial infections associated with inhaled corticosteroid use. Eur Respir J. 2017 Sep 20;50(3):1700037.[Abstract][Full Text]
107. Chalmers JD, Goeminne P, Aliberti S, et al. The bronchiectasis severity index. An international derivation and validation study. Am J Respir Crit Care Med. 2014 Mar 1;189(5):576-85.[Abstract][Full Text]
108. Ellis HC, Cowman S, Fernandes M, et al. Predicting mortality in bronchiectasis using bronchiectasis severity index and FACED scores: a 19-year cohort study. Eur Respir J. 2016 Feb;47(2):482-9.[Abstract]
109. McDonnell MJ, Aliberti S, Goeminne PC, et al. Multidimensional severity assessment in bronchiectasis: an analysis of seven European cohorts. Thorax. 2016 Dec;71(12):1110-8.[Abstract][Full Text]
110. Zhang P, Jiang G, Ding J, et al. Surgical treatment of bronchiectasis: a retrospective analysis of 790 patients. Ann Thorac Surg. 2010 Jul;90(1):246-50.[Abstract]
111. Bagheri R, Haghi SZ, Fattahi Massoum SH, et al. Surgical management of bronchiectasis: analysis of 277 patients. Thorac Cardiovasc Surg. 2010 Aug;58(5):291-4.[Abstract]
112. Haworth CS, Bilton D, Chalmers JD, et al. Inhaled liposomal ciprofloxacin in patients with non-cystic fibrosis bronchiectasis and chronic lung infection with Pseudomonas aeruginosa (ORBIT-3 and ORBIT-4): two phase 3, randomised controlled trials. Lancet Respir Med. 2019 Mar;7(3):213-26.[Abstract]
113. Chalmers JD, Cipolla D, Thompson B, et al. Changes in respiratory symptoms during 48-week treatment with ARD-3150 (inhaled liposomal ciprofloxacin) in bronchiectasis: results from the ORBIT-3 and -4 studies. Eur Respir J. 2020 Oct;56(4):2000110.[Abstract][Full Text]
114. De Soyza A, Aksamit T, Bandel TJ, et al. RESPIRE 1: a phase III placebo-controlled randomised trial of ciprofloxacin dry powder for inhalation in non-cystic fibrosis bronchiectasis. Eur Respir J. 2018 Jan 25;51(1):1702052.[Abstract][Full Text]
115. Aksamit T, De Soyza A, Bandel TJ, et al. RESPIRE 2: a phase III placebo-controlled randomised trial of ciprofloxacin dry powder for inhalation in non-cystic fibrosis bronchiectasis. Eur Respir J. 2018 Jan 25;51(1):1702053.[Abstract][Full Text]
116. Ailiyaer Y, Wang X, Zhang Y, et al. A prospective trial of nebulized amikacin in the treatment of bronchiectasis exacerbation. Respiration. 2018;95(5):327-33.[Abstract][Full Text]
117. Sibila O, Laserna E, Shoemark A, et al. Airway bacterial load and inhaled antibiotic response in bronchiectasis. Am J Respir Crit Care Med. 2019 Jul 1;200(1):33-41.[Abstract]
118. Bedi P, Chalmers JD, Graham C, et al. A randomized controlled trial of atorvastatin in patients with bronchiectasis infected with pseudomonas aeruginosa: a proof of concept study. Chest. 2017 Aug;152(2):368-78.[Abstract][Full Text]
119. Chalmers JD, Haworth CS, Metersky ML, et al. Phase 2 trial of the DPP-1 inhibitor brensocatib in bronchiectasis. N Engl J Med. 2020 Nov 26;383(22):2127-37.[Abstract][Full Text]
120. Chalmers JD, Chotirmall SH. Bronchiectasis: new therapies and new perspectives. Lancet Respir Med. 2018 Sep;6(9):715-26.[Abstract]
121. Chang AB, Oppenheimer JJ, Weinberger MM, et al. Use of management pathways or algorithms in children with chronic cough: CHEST guideline and expert panel report. Chest. 2017 Apr;151(4):875-83.[Abstract][Full Text]
122. Chalmers JD, Ringshausen FC, Harris B, et al. Cross-infection risk in patients with bronchiectasis: a position statement from the European Bronchiectasis Network (EMBARC), EMBARC/ELF patient advisory group and European Reference Network (ERN-Lung) Bronchiectasis Network. Eur Respir J. 2018 Jan 11;51(1):1701937.[Abstract][Full Text]
123. Pereira MC, Athanazio RA, Dalcin PTR, et al. Brazilian consensus on non-cystic fibrosis bronchiectasis. J Bras Pneumol. 2019 Aug 12;45(4):e20190122.[Abstract][Full Text]
124. Keistinen T, Saynajakangas O, Tuuponen T, et al. Bronchiectasis: an orphan disease with a poorly-understood prognosis. Eur Respir J. 1997 Dec;10(12):2784-7.[Abstract][Full Text]
125. Martinez-Garcia MA, Soler-Cataluna JJ, Perpina-Tordera M, et al. Factors associated with lung function decline in adult patients with stable non-cystic fibrosis bronchiectasis. Chest. 2007 Nov;132(5):1565-72.[Abstract]
126. Loebinger MR, Wells AU, Hansell DM, et al. Mortality in bronchiectasis: a long term study assessing the factors influencing survival. Eur Respir J. 2009 Oct;34(4):843-9.[Abstract]
127. Martinez-Garcia MA, Perpina-Tordera M, Roman-Sanchez P, et al. Quality-of-life determinants in patients with clinically stable bronchiectasis. Chest. 2005 Aug;128(2):739-45.[Abstract][Full Text]
128. Fartoukh M, Khalil A, Louis L, et al. An integrated approach to diagnosis and management of severe haemoptysis in patients admitted to the intensive care unit: a case series from a referral center. Respir Res. 2007 Feb 15;8:11.[Abstract][Full Text]
129. Serasli E, Kalpakidis V, Iatrou K, et al. Percutaneous bronchial artery embolization in the management of massive hemoptysis in chronic lung diseases. Immediate and long-term outcomes. Int Angiol. 2008 Aug;27(4):319-28.[Abstract]
130. Panda A, Bhalla AS, Goyal A. Bronchial artery embolization in hemoptysis: a systematic review. Diagn Interv Radiol. 2017 Jul-Aug;23(4):307-17.[Abstract][Full Text]
131. Chen YF, Lin HH, Lin CS, et al. Bronchiectasis and increased risk of ischemic stroke: a nationwide population-based cohort study. Int J Chron Obstruct Pulmon Dis. 2017 May 10;12:1375-83.[Abstract][Full Text]
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