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Erschienen in: Current Pulmonology Reports 3/2015

01.09.2015 | Bronchiectasis (G Tino, Section Editor)

Bronchiectasis in adults: epidemiology, assessment of severity and prognosis

verfasst von: James D. Chalmers

Erschienen in: Current Pulmonology Reports | Ausgabe 3/2015

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Abstract

This article reviews the epidemiology, severity and impact of bronchiectasis in adults. Bronchiectasis is an increasingly recognised clinical syndrome characterised by bronchial dilatation on CT scanning in association with a history of cough, sputum production and/or recurrent respiratory infections. It may complicate a large number of underlying disorders and is increasingly recognised in association with other airway diseases, including COPD. Important considerations in the epidemiology of bronchiectasis include our limited knowledge of how to define the disease and therefore a lack of large-scale epidemiological studies to define how common it is. The impact of the disease is considerable in terms of healthcare visits, antibiotic use, hospital admissions and mortality. The severity of disease varies greatly, from patients with infrequent exacerbations and few symptoms, to patients with hospital admissions, poor quality of life and greatly reduced survival. Rational therapy requires accurate severity assessment in order to identify those patients most likely to benefit. We have recently described a bronchiectasis severity index (BSI) which has been derived and validated in a multicentre international study and shown to predict mortality, hospital admissions, exacerbations and quality of life. Additional validation data have been published in the past 12 months demonstrating that the BSI accurately stratifies patients according to their disease burden and future risk.
Literatur
1.
Zurück zum Zitat Pasteur MC, Bilton D, Hill AT. British Thoracic Society guideline for non-CF bronchiectasis. Thorax. 2010;65 suppl 1:i1–i58.PubMedCrossRef Pasteur MC, Bilton D, Hill AT. British Thoracic Society guideline for non-CF bronchiectasis. Thorax. 2010;65 suppl 1:i1–i58.PubMedCrossRef
2.
Zurück zum Zitat Chalmers JD, Aliberti S, Blasi F. State of the art review: bronchiectasis in adults. Eur Respir J. 2015;45(5):1446–62.PubMedCrossRef Chalmers JD, Aliberti S, Blasi F. State of the art review: bronchiectasis in adults. Eur Respir J. 2015;45(5):1446–62.PubMedCrossRef
3.
Zurück zum Zitat Kang EY, Miller RR, Muller NL. Bronchiectasis: comparison of preoperative thin-section CT and pathologic findings in resected specimens. Radiology. 1995;195:649–54.PubMedCrossRef Kang EY, Miller RR, Muller NL. Bronchiectasis: comparison of preoperative thin-section CT and pathologic findings in resected specimens. Radiology. 1995;195:649–54.PubMedCrossRef
5.
Zurück zum Zitat Kelly MG, Murphy S, Elborn JS. Bronchiectasis in secondary care: a comprehensive profile of a neglected disease. Eur J Intern Med. 2003;14(8):488–92.PubMedCrossRef Kelly MG, Murphy S, Elborn JS. Bronchiectasis in secondary care: a comprehensive profile of a neglected disease. Eur J Intern Med. 2003;14(8):488–92.PubMedCrossRef
7.
Zurück zum Zitat Serisier DJ. The evidence base for non-CF bronchiectasis is finally evolving. Respirology. 2014;19(3):295–7.PubMedCrossRef Serisier DJ. The evidence base for non-CF bronchiectasis is finally evolving. Respirology. 2014;19(3):295–7.PubMedCrossRef
8.
Zurück zum Zitat Yap VL, Metersky ML. New therapeutic options for noncystic fibrosis bronchiectasis. Curr Opin Infect Dis. 2015;28(2):171–6.PubMedCrossRef Yap VL, Metersky ML. New therapeutic options for noncystic fibrosis bronchiectasis. Curr Opin Infect Dis. 2015;28(2):171–6.PubMedCrossRef
9.
Zurück zum Zitat Bronchiectasis. The European Lung White Book 2014; 15: 176–183. Bronchiectasis. The European Lung White Book 2014; 15: 176–183.
10.
Zurück zum Zitat Seitz AE, Olivier KN, Adjemian J, Holland SM, Prevots R. Trends in bronchiectasis among medicare beneficiaries in the United States, 2000 to 2007. Chest. 2012;142(2):432–9.PubMedCrossRefPubMedCentral Seitz AE, Olivier KN, Adjemian J, Holland SM, Prevots R. Trends in bronchiectasis among medicare beneficiaries in the United States, 2000 to 2007. Chest. 2012;142(2):432–9.PubMedCrossRefPubMedCentral
11.
Zurück zum Zitat Chang AB, Brown N, Toombs M, Marsh RL, Redding GJ. Lung disease in indigenous children. Paediatr Respir Rev. 2014;15(4):325–32.PubMed Chang AB, Brown N, Toombs M, Marsh RL, Redding GJ. Lung disease in indigenous children. Paediatr Respir Rev. 2014;15(4):325–32.PubMed
12.
Zurück zum Zitat McShane PJ, Naureckas ET, Strek ME. Bronchiectasis in a diverse US population: effects of ethnicity on etiology and sputum culture. Chest. 2012;142(1):159–67.PubMedCrossRef McShane PJ, Naureckas ET, Strek ME. Bronchiectasis in a diverse US population: effects of ethnicity on etiology and sputum culture. Chest. 2012;142(1):159–67.PubMedCrossRef
13.
Zurück zum Zitat Hester KLM, MacFarlane JG, Tedd H, et al. Fatigue in bronchiectasis. Q J Med. 2012;105:235–40.CrossRef Hester KLM, MacFarlane JG, Tedd H, et al. Fatigue in bronchiectasis. Q J Med. 2012;105:235–40.CrossRef
14.
Zurück zum Zitat Wilson CB, Jones PW, O’Leary CJ, Hansell DM, Cole PJ, Wilson R. Effect of sputum bacteriology on the quality of life of patients with bronchiectasis. Eur Respir J. 1997;10:1754–60.PubMedCrossRef Wilson CB, Jones PW, O’Leary CJ, Hansell DM, Cole PJ, Wilson R. Effect of sputum bacteriology on the quality of life of patients with bronchiectasis. Eur Respir J. 1997;10:1754–60.PubMedCrossRef
15.
Zurück zum Zitat Hernandez C, Abreu J, Jimenez A, et al. Función pulmonar y calidad de vida en relación con la colonización bronquial en adultos con bronquiectasias no debidas a fibrosis quística. Med Clin (Barc). 2002;118(4):130–4.CrossRef Hernandez C, Abreu J, Jimenez A, et al. Función pulmonar y calidad de vida en relación con la colonización bronquial en adultos con bronquiectasias no debidas a fibrosis quística. Med Clin (Barc). 2002;118(4):130–4.CrossRef
16.
Zurück zum Zitat Ho PL, Chan KN, Ip MSM, et al. The effect of Pseudomonas aeruginosa infection on clinical parameters in steady-state bronchiectasis. Chest. 1998;114:1594–8.PubMedCrossRef Ho PL, Chan KN, Ip MSM, et al. The effect of Pseudomonas aeruginosa infection on clinical parameters in steady-state bronchiectasis. Chest. 1998;114:1594–8.PubMedCrossRef
18.
Zurück zum Zitat Weycker D, Edelsberg J, Oster G, Tine G. Prevalence and economic burden of bronchiectasis. Clin Pulm Med. 2005;12:205–9.CrossRef Weycker D, Edelsberg J, Oster G, Tine G. Prevalence and economic burden of bronchiectasis. Clin Pulm Med. 2005;12:205–9.CrossRef
20.
Zurück zum Zitat O’Brien C, Guest PJ, Hill SL, Stockley RA. Physiological and radiological characterisation of patients diagnosed with chronic obstructive pulmonary disease in primary care. Thorax. 2000;55:635–42.PubMedCrossRefPubMedCentral O’Brien C, Guest PJ, Hill SL, Stockley RA. Physiological and radiological characterisation of patients diagnosed with chronic obstructive pulmonary disease in primary care. Thorax. 2000;55:635–42.PubMedCrossRefPubMedCentral
22.
Zurück zum Zitat Copley SJ, Wells AU, Hawtin KE, Gibson DJ, Hodson JM, Jacques AE, et al. Lung morphology in the elderly: comparative CT study of subjects over 75 years old versus those under 55 years old. Radiology. 2009;251(2):566–73. doi:10.1148/radiol.2512081242.PubMedCrossRef Copley SJ, Wells AU, Hawtin KE, Gibson DJ, Hodson JM, Jacques AE, et al. Lung morphology in the elderly: comparative CT study of subjects over 75 years old versus those under 55 years old. Radiology. 2009;251(2):566–73. doi:10.​1148/​radiol.​2512081242.PubMedCrossRef
23.
Zurück zum Zitat Mandal P, Chalmers JD, Graham C, Harley C, Sidhu MK, Doherty C, et al. Atorvastatin as a stable treatment in bronchiectasis: a randomised controlled trial. Lancet Respir Med. 2014;2(6):455–63.PubMedCrossRef Mandal P, Chalmers JD, Graham C, Harley C, Sidhu MK, Doherty C, et al. Atorvastatin as a stable treatment in bronchiectasis: a randomised controlled trial. Lancet Respir Med. 2014;2(6):455–63.PubMedCrossRef
24.
Zurück zum Zitat Bedi P, Sidhu MK, Donaldson LS, Chalmers JD, Smith MP, Turnbull K, et al. A Prospective cohort study of the use of domicillary intravenous antibiotics in bronchiectasis. NPJ Prim Care Respir Med. 2014;24:14090.PubMed Bedi P, Sidhu MK, Donaldson LS, Chalmers JD, Smith MP, Turnbull K, et al. A Prospective cohort study of the use of domicillary intravenous antibiotics in bronchiectasis. NPJ Prim Care Respir Med. 2014;24:14090.PubMed
25.
Zurück zum Zitat Pasteur MC, Helliwell SM, Houghton SJ, Webb SC, Foweraker JE, Coulden RA, et al. An investigation into causative factors in patients with bronchiectasis. Am J Respir Crit Care Med. 2000;162:1277–84.PubMedCrossRef Pasteur MC, Helliwell SM, Houghton SJ, Webb SC, Foweraker JE, Coulden RA, et al. An investigation into causative factors in patients with bronchiectasis. Am J Respir Crit Care Med. 2000;162:1277–84.PubMedCrossRef
26.
Zurück zum Zitat Shoemark A, Ozerovitch L, Wilson R. Aetiology in adult patients with bronchiectasis. Respir Med. 2007;101:1163–70.PubMedCrossRef Shoemark A, Ozerovitch L, Wilson R. Aetiology in adult patients with bronchiectasis. Respir Med. 2007;101:1163–70.PubMedCrossRef
27.
Zurück zum Zitat King PT, Holdsworth SR, Farmer M, Freezer N, Villaneuva E, Holmes PW. Phenotypes of adult bronchiectasis: onset of productive cough in childhood and adulthood. COPD. 2009;6(2):130–6.PubMedCrossRef King PT, Holdsworth SR, Farmer M, Freezer N, Villaneuva E, Holmes PW. Phenotypes of adult bronchiectasis: onset of productive cough in childhood and adulthood. COPD. 2009;6(2):130–6.PubMedCrossRef
28.
Zurück zum Zitat Shah PL, Mawdsley S, Nash K, Cullinan P, Cole PJ, Wilson R. Determinants of chronic infection with Staphylococcus aureus in patients with bronchiectasis. Eur Respir J. 1999;14(6):1340–4.PubMedCrossRef Shah PL, Mawdsley S, Nash K, Cullinan P, Cole PJ, Wilson R. Determinants of chronic infection with Staphylococcus aureus in patients with bronchiectasis. Eur Respir J. 1999;14(6):1340–4.PubMedCrossRef
29.
Zurück zum Zitat Hill SL, Mitchell JL, Burnett D, Stockley RA. IgG subclasses in the serum and sputum from patients with bronchiectasis. Thorax. 1998;53(6):463–8.PubMedCrossRefPubMedCentral Hill SL, Mitchell JL, Burnett D, Stockley RA. IgG subclasses in the serum and sputum from patients with bronchiectasis. Thorax. 1998;53(6):463–8.PubMedCrossRefPubMedCentral
30.
Zurück zum Zitat De Gracia J, Rodrigo MJ, Morell F, Vendrell M, Miravitlles M, Cruz MJ, et al. IgG subclass deficiencies associated with bronchiectasis. Am J Respir Crit Care Med. 1996;153(2):650–5.PubMedCrossRef De Gracia J, Rodrigo MJ, Morell F, Vendrell M, Miravitlles M, Cruz MJ, et al. IgG subclass deficiencies associated with bronchiectasis. Am J Respir Crit Care Med. 1996;153(2):650–5.PubMedCrossRef
32.
Zurück zum Zitat Swinson DR, Symmons D, Suresh U, Jones M, Booth J. Decreased survival in patients with co-existent rheumatoid arthritis and bronchiectasis. Br J Rheumatol. 1997;36(6):689–91.PubMedCrossRef Swinson DR, Symmons D, Suresh U, Jones M, Booth J. Decreased survival in patients with co-existent rheumatoid arthritis and bronchiectasis. Br J Rheumatol. 1997;36(6):689–91.PubMedCrossRef
34.
Zurück zum Zitat Soto-Cardenas MJ, Perez-De-Lis M, Bove A, Navarro C, Brito-Zeron P, Diaz-Lagares C, et al. Bronchiectasis in primary Sjögren’s syndrome: prevalence and clinical significance. Clin Exp Rheumatol. 2010;28(5):647–53.PubMed Soto-Cardenas MJ, Perez-De-Lis M, Bove A, Navarro C, Brito-Zeron P, Diaz-Lagares C, et al. Bronchiectasis in primary Sjögren’s syndrome: prevalence and clinical significance. Clin Exp Rheumatol. 2010;28(5):647–53.PubMed
36.
Zurück zum Zitat Martínez-García MA, de la Rosa Carrillo D, Soler-Cataluña JJ, Donat-Sanz Y, Serra PC, Lerma MA, et al. Prognostic value of bronchiectasis in patients with moderate-to-severe chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2013;187(8):823–31. doi:10.1164/rccm.201208-1518OC.PubMedCrossRef Martínez-García MA, de la Rosa Carrillo D, Soler-Cataluña JJ, Donat-Sanz Y, Serra PC, Lerma MA, et al. Prognostic value of bronchiectasis in patients with moderate-to-severe chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2013;187(8):823–31. doi:10.​1164/​rccm.​201208-1518OC.PubMedCrossRef
37.
Zurück zum Zitat Agusti A, Calverley PM, Celli B, Coxson HO, Edwards LD, Lomas D, et al. Characterisation of COPD heterogeneity in the ECLIPSE cohort. Respir Res. 2010;11(3):122.PubMedPubMedCentral Agusti A, Calverley PM, Celli B, Coxson HO, Edwards LD, Lomas D, et al. Characterisation of COPD heterogeneity in the ECLIPSE cohort. Respir Res. 2010;11(3):122.PubMedPubMedCentral
38.
Zurück zum Zitat Stewart JL, Maselli DJ, Anzueto A, Criner GJ, Han MK, Martinez FJ, et al. COPDgene investigators. Clinical impact of CT radiological feature of bronchiectasis in the COPDgene cohort. Am J Respir Crit Care Med. 2012;185:A3656.CrossRef Stewart JL, Maselli DJ, Anzueto A, Criner GJ, Han MK, Martinez FJ, et al. COPDgene investigators. Clinical impact of CT radiological feature of bronchiectasis in the COPDgene cohort. Am J Respir Crit Care Med. 2012;185:A3656.CrossRef
39.
Zurück zum Zitat Uzun S, Djamin RS, Kluytmans JA, Mulder PG, van’t Veer NE, Ermens AA, et al. Azithromycin maintenance treatment in patients with frequent exacerbations of chronic obstructive pulmonary disease (COLUMBUS): a randomised, double-blind, placebo-controlled trial. Lancet Respir Med. 2014;2(5):361–8. doi:10.1016/S2213-2600(14)70019-0.PubMedCrossRef Uzun S, Djamin RS, Kluytmans JA, Mulder PG, van’t Veer NE, Ermens AA, et al. Azithromycin maintenance treatment in patients with frequent exacerbations of chronic obstructive pulmonary disease (COLUMBUS): a randomised, double-blind, placebo-controlled trial. Lancet Respir Med. 2014;2(5):361–8. doi:10.​1016/​S2213-2600(14)70019-0.PubMedCrossRef
40.
Zurück zum Zitat Jairam PM, van der Graaf Y, Lammers JW, Mali WP, de Jong PA. PROVIDI Study group. Incidental findings on chest CT imaging are associated with increased COPD exacerbations and mortality. Thorax. 2015. doi:10.1136/thoraxjnl-2014-206160.PubMed Jairam PM, van der Graaf Y, Lammers JW, Mali WP, de Jong PA. PROVIDI Study group. Incidental findings on chest CT imaging are associated with increased COPD exacerbations and mortality. Thorax. 2015. doi:10.​1136/​thoraxjnl-2014-206160.PubMed
41.
Zurück zum Zitat Jones RC, Price D, Ryan D, Sims EJ, von Ziegenweidt J, Mascarenhas L, et al. Opportunities to diagnose chronic obstructive pulmonary disease in routine care in the UK: a retrospective study of a clinical cohort. Lancet Respir Med. 2014;2(4):267–76. doi:10.1016/S2213-2600(14)70008-6.PubMedCrossRef Jones RC, Price D, Ryan D, Sims EJ, von Ziegenweidt J, Mascarenhas L, et al. Opportunities to diagnose chronic obstructive pulmonary disease in routine care in the UK: a retrospective study of a clinical cohort. Lancet Respir Med. 2014;2(4):267–76. doi:10.​1016/​S2213-2600(14)70008-6.PubMedCrossRef
42.
Zurück zum Zitat Goeminne PC, Nawrot TS, Ruttens D, Seys S, Dupont LJ. Mortality in non-cystic fibrosis bronchiectasis: a prospective cohort analysis. Respir Med. 2014;108(2):287–96.PubMedCrossRef Goeminne PC, Nawrot TS, Ruttens D, Seys S, Dupont LJ. Mortality in non-cystic fibrosis bronchiectasis: a prospective cohort analysis. Respir Med. 2014;108(2):287–96.PubMedCrossRef
43.
Zurück zum Zitat Chalmers JD, Goeminne P, Aliberti S, et al. Derivation and validation of the bronchiectasis severity index: an international multicentre observational study. Am J Respir Crit Care Med. 2014;189(5):576–85.PubMedCrossRefPubMedCentral Chalmers JD, Goeminne P, Aliberti S, et al. Derivation and validation of the bronchiectasis severity index: an international multicentre observational study. Am J Respir Crit Care Med. 2014;189(5):576–85.PubMedCrossRefPubMedCentral
44.
Zurück zum Zitat Chalmers JD, Akram AR, Hill AT. Increasing outpatient treatment of mild community-acquired pneumonia: systematic review and meta-analysis. Eur Respir J. 2011;37(4):858–64.PubMedCrossRef Chalmers JD, Akram AR, Hill AT. Increasing outpatient treatment of mild community-acquired pneumonia: systematic review and meta-analysis. Eur Respir J. 2011;37(4):858–64.PubMedCrossRef
45.
Zurück zum Zitat Du Bois RM, Weycker D, Albera C, Bradford WZ, Costabel U, Kartashov A, et al. Ascertainment of individual risk of mortality for patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2011;184(4):459–66.PubMedCrossRef Du Bois RM, Weycker D, Albera C, Bradford WZ, Costabel U, Kartashov A, et al. Ascertainment of individual risk of mortality for patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2011;184(4):459–66.PubMedCrossRef
46.
Zurück zum Zitat Singanayagam A, Schembri S, Chalmers JD. Predictors of mortality in hospitalized adults with acute exacerbation of chronic obstructive pulmonary disease. Ann Am Thoracic Soc. 2013;10(2):81–9.CrossRef Singanayagam A, Schembri S, Chalmers JD. Predictors of mortality in hospitalized adults with acute exacerbation of chronic obstructive pulmonary disease. Ann Am Thoracic Soc. 2013;10(2):81–9.CrossRef
47.
48.
Zurück zum Zitat Falk G, Fahey T. Clinical prediction rules. BMJ 2009; 339 Falk G, Fahey T. Clinical prediction rules. BMJ 2009; 339
49.
Zurück zum Zitat Toll DB, Janssen KJ, Vergouwe Y, Moons KG. Validation, updating and impact of clinical prediction rules: a review. J Clin Epidemiol. 2008;61(11):1085–94.PubMedCrossRef Toll DB, Janssen KJ, Vergouwe Y, Moons KG. Validation, updating and impact of clinical prediction rules: a review. J Clin Epidemiol. 2008;61(11):1085–94.PubMedCrossRef
52.
Zurück zum Zitat Morice AH, Millqvist E, Belvisi MG, Bieksiene K, Birring SS, Chung KF, et al. Expert opinion on the cough hypersensitivity syndrome in respiratory medicine. Eur Respir J. 2014;44(5):1132–48.PubMedCrossRef Morice AH, Millqvist E, Belvisi MG, Bieksiene K, Birring SS, Chung KF, et al. Expert opinion on the cough hypersensitivity syndrome in respiratory medicine. Eur Respir J. 2014;44(5):1132–48.PubMedCrossRef
53.
Zurück zum Zitat Guan WJ, Gao YH, Xu G, Lin ZY, Tang Y, Li HM, et al. Impulse oscillometry in adults with bronchiectasis. Ann Am Thorac Soc. 2015;12(5):657–65.PubMedCrossRef Guan WJ, Gao YH, Xu G, Lin ZY, Tang Y, Li HM, et al. Impulse oscillometry in adults with bronchiectasis. Ann Am Thorac Soc. 2015;12(5):657–65.PubMedCrossRef
54.
55.
Zurück zum Zitat Bradley JM, Wilson JJ, Hayes K, Kent L, McDonough S, Tully MA, et al. Sedentary behaviour and physical activity in bronchiectasis. A cross-sectional study. BMC Pulm Med. 2015;15(1):61.PubMedCrossRefPubMedCentral Bradley JM, Wilson JJ, Hayes K, Kent L, McDonough S, Tully MA, et al. Sedentary behaviour and physical activity in bronchiectasis. A cross-sectional study. BMC Pulm Med. 2015;15(1):61.PubMedCrossRefPubMedCentral
56.
Zurück zum Zitat Martinez-Garcia MA, de Gracia J, Vendrell Relat M, et al. Multidomensional approach to non-cystic fibrosis bronchiectasis; the FACED score. Eur Respir J. 2014;43(5):1357–67.PubMedCrossRef Martinez-Garcia MA, de Gracia J, Vendrell Relat M, et al. Multidomensional approach to non-cystic fibrosis bronchiectasis; the FACED score. Eur Respir J. 2014;43(5):1357–67.PubMedCrossRef
57.
Zurück zum Zitat Loebinger MR, Wells AU, Hansell DM, Chinyanganya N, Devaraj A, Meister M, et al. Mortality in bronchiectasis: a long-term study assessing the factors influencing survival. Eur Respir J. 2009;34(4):843–9.PubMedCrossRef Loebinger MR, Wells AU, Hansell DM, Chinyanganya N, Devaraj A, Meister M, et al. Mortality in bronchiectasis: a long-term study assessing the factors influencing survival. Eur Respir J. 2009;34(4):843–9.PubMedCrossRef
58.
Zurück zum Zitat Evans SA, Turner SM, Bosch BJ, Hardy CC, Woodhead MA. Lung function in bronchiectasis:the influence of Pseudomonas aeruginosa. Eur Respir J. 1996;9(8):1601–4.PubMedCrossRef Evans SA, Turner SM, Bosch BJ, Hardy CC, Woodhead MA. Lung function in bronchiectasis:the influence of Pseudomonas aeruginosa. Eur Respir J. 1996;9(8):1601–4.PubMedCrossRef
59.
Zurück zum Zitat Davies G, Wells AU, Doffman S, Watanabe S, Wilson R. The effect of Pseudomonas aeruginosa on pulmonary function in patients with bronchiectasis. Eur Respir J. 2006;28(5):974–9.PubMedCrossRef Davies G, Wells AU, Doffman S, Watanabe S, Wilson R. The effect of Pseudomonas aeruginosa on pulmonary function in patients with bronchiectasis. Eur Respir J. 2006;28(5):974–9.PubMedCrossRef
60.
Zurück zum Zitat King PT, Holdsworth SR, Freezer NJ, et al. Microbiologic follow-up study in adult bronchiectasis. Respir Med. 2007;101:1633–8.PubMedCrossRef King PT, Holdsworth SR, Freezer NJ, et al. Microbiologic follow-up study in adult bronchiectasis. Respir Med. 2007;101:1633–8.PubMedCrossRef
61.•
Zurück zum Zitat Haworth CS, Foweraker JE, Wilkinson P, Kenyon RF, Bilton D. Inhaled colistin in patients with bronchiectasis and chronic pseudomonas aeruginosa infection. Am J Respir Crit Care Med. 2014;189(8):975–82. Large randomized controlled trial notable for failing to meet its primary end-point of time to next exacerbation, but nevertheless showing that inhaled antibiotics greatly improved quality of life and time to next exacerbation in compliant patients. Haworth CS, Foweraker JE, Wilkinson P, Kenyon RF, Bilton D. Inhaled colistin in patients with bronchiectasis and chronic pseudomonas aeruginosa infection. Am J Respir Crit Care Med. 2014;189(8):975–82. Large randomized controlled trial notable for failing to meet its primary end-point of time to next exacerbation, but nevertheless showing that inhaled antibiotics greatly improved quality of life and time to next exacerbation in compliant patients.
62.
Zurück zum Zitat Serisier DJ, Bilton D, De Soyza A, et al. Inhaled, dual release liposomal ciprofloxacin in non-cystic fibrosis bronchiectasis (ORBIT-2): a randomised, double-blind, placebo-controlled trial. Thorax. 2013;68(9):812–7.PubMedCrossRef Serisier DJ, Bilton D, De Soyza A, et al. Inhaled, dual release liposomal ciprofloxacin in non-cystic fibrosis bronchiectasis (ORBIT-2): a randomised, double-blind, placebo-controlled trial. Thorax. 2013;68(9):812–7.PubMedCrossRef
63.
Zurück zum Zitat Tunney MM, Einarsson GG, Wei L, et al. Lung microbiota and bacterial abundance in patients with bronchiectasis when clinically stable and during exacerbation. Am J Respir Crit Care Med. 2013;187(10):1118–26.PubMedCrossRefPubMedCentral Tunney MM, Einarsson GG, Wei L, et al. Lung microbiota and bacterial abundance in patients with bronchiectasis when clinically stable and during exacerbation. Am J Respir Crit Care Med. 2013;187(10):1118–26.PubMedCrossRefPubMedCentral
64.
Zurück zum Zitat Rogers GB, van der Gast CJ, Cuthbertson L, et al. Clinical measures of disease in adult non-CF bronchiectasis correlate with airway microbiota composition. Thorax. 2013;68(8):731–7.PubMedCrossRef Rogers GB, van der Gast CJ, Cuthbertson L, et al. Clinical measures of disease in adult non-CF bronchiectasis correlate with airway microbiota composition. Thorax. 2013;68(8):731–7.PubMedCrossRef
65.•
Zurück zum Zitat Rogers GB, Zain NM, Bruce KD, et al. A novel microbiota stratification system predicts future exacerbations in bronchiectasis. Ann Am Thorac Soc. 2014;11(4):496–503. One of the largest studies of the microbiome in bronchiectasis providing interesting data comparing culture, PCR and sequencing methods of microbiology testing and their relationship with clinical parameters. Rogers GB, Zain NM, Bruce KD, et al. A novel microbiota stratification system predicts future exacerbations in bronchiectasis. Ann Am Thorac Soc. 2014;11(4):496–503. One of the largest studies of the microbiome in bronchiectasis providing interesting data comparing culture, PCR and sequencing methods of microbiology testing and their relationship with clinical parameters.
66.
Zurück zum Zitat Chalmers JD, Smith MP, McHugh B, Doherty C, Govan JRW, Hill AT. Short and long term antibiotic therapy reduces airway and systemic inflammation in non-CF bronchiectasis. Am J Respir Crit Care Med. 2012;186(7):657–65.PubMedCrossRef Chalmers JD, Smith MP, McHugh B, Doherty C, Govan JRW, Hill AT. Short and long term antibiotic therapy reduces airway and systemic inflammation in non-CF bronchiectasis. Am J Respir Crit Care Med. 2012;186(7):657–65.PubMedCrossRef
67.
Zurück zum Zitat McDonnell MK, Jary HR, Perry A, et al. Non cystic fibrosis bronchiectasis: a longitudinal retrospective observational cohort study of Pseudomonas persistence and resistance. Respir Med. 2015;109(6):716–26.PubMedCrossRef McDonnell MK, Jary HR, Perry A, et al. Non cystic fibrosis bronchiectasis: a longitudinal retrospective observational cohort study of Pseudomonas persistence and resistance. Respir Med. 2015;109(6):716–26.PubMedCrossRef
68.
Zurück zum Zitat Chalmers JD, Hill AT. Mechanisms of immune dysfunction and bacterial persistence in non-cystic fibrosis bronchiectasis. Mol Immunol. 2013;55:27–34.PubMedCrossRef Chalmers JD, Hill AT. Mechanisms of immune dysfunction and bacterial persistence in non-cystic fibrosis bronchiectasis. Mol Immunol. 2013;55:27–34.PubMedCrossRef
69.
Zurück zum Zitat Quigley KJ, Reynolds CJ, Goudet A, Raynsford EJ, Sergeant R, Quigley A, Worgall S, Bilton D, Wilson R, Loebinger MR, Maillere B, Altmann DM, Boyton RJ. Chronic Infection by Mucoid Pseudomonas aeruginosa Associated with Dysregulation in T Cell Immunity to OprF. Am J Respir Crit Care Med. 2015. Quigley KJ, Reynolds CJ, Goudet A, Raynsford EJ, Sergeant R, Quigley A, Worgall S, Bilton D, Wilson R, Loebinger MR, Maillere B, Altmann DM, Boyton RJ. Chronic Infection by Mucoid Pseudomonas aeruginosa Associated with Dysregulation in T Cell Immunity to OprF. Am J Respir Crit Care Med. 2015.
70.•
Zurück zum Zitat Wells TJ, Whitters D, Sevastsyanovich YR, Heath JN, Pravin J, Goodall M, et al. Increased severity of respiratory infections associated with elevated anti-LPS IgG2 which inhibits serum bactericidal killing. J Exp Med. 2014;211(9):1893–904. doi:10.1084/jem.20132444. Important study that has identified a novel mechanism leading to Pseudomonas aeruginosa colonisation, and suggesting a possible treatment through the removal of blocking IgG. Wells TJ, Whitters D, Sevastsyanovich YR, Heath JN, Pravin J, Goodall M, et al. Increased severity of respiratory infections associated with elevated anti-LPS IgG2 which inhibits serum bactericidal killing. J Exp Med. 2014;211(9):1893–904. doi:10.​1084/​jem.​20132444. Important study that has identified a novel mechanism leading to Pseudomonas aeruginosa colonisation, and suggesting a possible treatment through the removal of blocking IgG.
71.
Zurück zum Zitat Mandal P, Morice AH, Chalmers JD, Hill AT. Symptoms of airway reflux predict exacerbations and quality of life in bronchiectasis. Respir Med. 2013;107(7):1008–13.PubMedCrossRef Mandal P, Morice AH, Chalmers JD, Hill AT. Symptoms of airway reflux predict exacerbations and quality of life in bronchiectasis. Respir Med. 2013;107(7):1008–13.PubMedCrossRef
72.
Zurück zum Zitat McDonnell MJ, Ahmed M, Das J, et al. Hiatus hernias are correlated with increased severity of non-cystic fibrosis bronchiectasis. Respirology. 2015. doi:10.1111/resp 12522.PubMed McDonnell MJ, Ahmed M, Das J, et al. Hiatus hernias are correlated with increased severity of non-cystic fibrosis bronchiectasis. Respirology. 2015. doi:10.​1111/​resp 12522.PubMed
74.
Zurück zum Zitat Chalmers JD, McHugh BJ, Doherty CJ, Govan JR, Hill AT. Vitamin-D deficiency is associated with chronic bacterial colonisation and disease severity in non-CF bronchiectasis. Thorax. 2012;68(1):39–47.PubMedCrossRef Chalmers JD, McHugh BJ, Doherty CJ, Govan JR, Hill AT. Vitamin-D deficiency is associated with chronic bacterial colonisation and disease severity in non-CF bronchiectasis. Thorax. 2012;68(1):39–47.PubMedCrossRef
76.
Zurück zum Zitat Martineau AR, MacLaughlin BD, Hooper RL, Barnes NC, Jolliffe DA, Greiller CL, et al. Double-blind randomised placebo-controlled trial of bolus-dose vitamin D3 supplementation in adults with asthma (ViDiAs). Thorax. 2015;70(5):451–7. doi:10.1136/thoraxjnl-2014-206449.PubMedCrossRef Martineau AR, MacLaughlin BD, Hooper RL, Barnes NC, Jolliffe DA, Greiller CL, et al. Double-blind randomised placebo-controlled trial of bolus-dose vitamin D3 supplementation in adults with asthma (ViDiAs). Thorax. 2015;70(5):451–7. doi:10.​1136/​thoraxjnl-2014-206449.PubMedCrossRef
78.
Zurück zum Zitat Taylor SL, Rogers GB, Chen AC, Burr LD, McGuckin MA, Serisier DJ. Matrix metalloproteinases vary with airway microbiota composition and lung function in non-cystic fibrosis bronchiectasis. Ann Am Thorac Soc. 2015;12(5):701–7. doi:10.1513/AnnalsATS.201411-513OC.PubMedCrossRef Taylor SL, Rogers GB, Chen AC, Burr LD, McGuckin MA, Serisier DJ. Matrix metalloproteinases vary with airway microbiota composition and lung function in non-cystic fibrosis bronchiectasis. Ann Am Thorac Soc. 2015;12(5):701–7. doi:10.​1513/​AnnalsATS.​201411-513OC.PubMedCrossRef
79.
Zurück zum Zitat Slieker MG, Sanders EA, Rijkers GT, Ruven HJ, van der Ent CK. Disease modifying genes in cystic fibrosis. J Cyst Fibros. 2005;4 Suppl 2:7–13.PubMedCrossRef Slieker MG, Sanders EA, Rijkers GT, Ruven HJ, van der Ent CK. Disease modifying genes in cystic fibrosis. J Cyst Fibros. 2005;4 Suppl 2:7–13.PubMedCrossRef
80.
Zurück zum Zitat Chalmers JD, Fleming GB, Hill AT, Kilpatrick DC. Impact of mannose binding lectin (MBL) insufficiency on the course of cystic fibrosis: a review and meta-analysis. Glycobiology. 2011;21(3):271–82.PubMedCrossRef Chalmers JD, Fleming GB, Hill AT, Kilpatrick DC. Impact of mannose binding lectin (MBL) insufficiency on the course of cystic fibrosis: a review and meta-analysis. Glycobiology. 2011;21(3):271–82.PubMedCrossRef
81.
Zurück zum Zitat Chalmers JD, McHugh BJ, Doherty C, et al. Mannose binding lectin deficiency and disease severity in non-cystic fibrosis bronchiectasis: a prospective study. Lancet Respir Med. 2013;1(3):224–32.PubMedCrossRef Chalmers JD, McHugh BJ, Doherty C, et al. Mannose binding lectin deficiency and disease severity in non-cystic fibrosis bronchiectasis: a prospective study. Lancet Respir Med. 2013;1(3):224–32.PubMedCrossRef
84.
Zurück zum Zitat Boyton RJ, Smith J, Ward R, Jones M, Ozerovitch L, Wilson R, et al. HLA-C and killer cell immunoglobulin-like receptor genes in idiopathic bronchiectasis. Am J Respir Crit Care Med. 2006;173(3):327–33.PubMedCrossRef Boyton RJ, Smith J, Ward R, Jones M, Ozerovitch L, Wilson R, et al. HLA-C and killer cell immunoglobulin-like receptor genes in idiopathic bronchiectasis. Am J Respir Crit Care Med. 2006;173(3):327–33.PubMedCrossRef
86.
Zurück zum Zitat Winthrop KL, Aksamit TR, Olivier KN, et al. The respiratory microbiology of patients with nontuberculous mycobacteria from the United States Bronchiectasis Research Registry. Am J Respir Crit Care Med. 2013;187:A4541. Winthrop KL, Aksamit TR, Olivier KN, et al. The respiratory microbiology of patients with nontuberculous mycobacteria from the United States Bronchiectasis Research Registry. Am J Respir Crit Care Med. 2013;187:A4541.
Metadaten
Titel
Bronchiectasis in adults: epidemiology, assessment of severity and prognosis
verfasst von
James D. Chalmers
Publikationsdatum
01.09.2015
Verlag
Springer US
Erschienen in
Current Pulmonology Reports / Ausgabe 3/2015
Elektronische ISSN: 2199-2428
DOI
https://doi.org/10.1007/s13665-015-0120-x

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