메뉴 건너뛰기




Volumn 36, Issue 2, 2015, Pages 267-286

Inhaled antibiotics in cystic fibrosis (CF) and non-CF bronchiectasis

Author keywords

antibiotics; cystic fibrosis; inhaled; nebulized; non CF bronchiectasis; Pseudomonas aeruginosa

Indexed keywords

AMIKACIN; ANTIBIOTIC AGENT; AZTREONAM; AZTREONAM LYSINE; CIPROFLOXACIN; COLISTIMETHATE; COLISTIN; FOSFOMYCIN; GENTAMICIN; LEVOFLOXACIN; TOBRAMYCIN; VANCOMYCIN; ANTIINFECTIVE AGENT;

EID: 84926350436     PISSN: 10693424     EISSN: 10989048     Source Type: Journal    
DOI: 10.1055/s-0035-1547346     Document Type: Article
Times cited : (28)

References (126)
  • 1
    • 0022531170 scopus 로고
    • Inflammation: A two-edged sword-the model of bronchiectasis
    • Cole P. J. Inflammation: a two-edged sword-the model of bronchiectasis. Eur J Respir Dis Suppl: 1986; 147 6 15
    • (1986) Eur J Respir Dis Suppl , vol.147 , pp. 6-15
    • Cole, P.J.1
  • 2
    • 84875625613 scopus 로고    scopus 로고
    • Mechanisms of immune dysfunction and bacterial persistence in non-cystic fibrosis bronchiectasis
    • Chalmers J. D., Hill A. T. Mechanisms of immune dysfunction and bacterial persistence in non-cystic fibrosis bronchiectasis. Mol Immunol: 2013; 55 1 27 34
    • (2013) Mol Immunol , vol.55 , Issue.1 , pp. 27-34
    • Chalmers, J.D.1    Hill, A.T.2
  • 3
    • 0031847529 scopus 로고    scopus 로고
    • Increases in CD4+ T lymphocytes, macrophages, neutrophils and interleukin 8 positive cells in the airways of patients with bronchiectasis
    • Gaga M., Bentley A. M., Humbert M., et al. Increases in CD4+ T lymphocytes, macrophages, neutrophils and interleukin 8 positive cells in the airways of patients with bronchiectasis. Thorax: 1998; 53 8 685 691
    • (1998) Thorax , vol.53 , Issue.8 , pp. 685-691
    • Gaga, M.1    Bentley, A.M.2    Humbert, M.3
  • 4
    • 84926380601 scopus 로고    scopus 로고
    • Available at: Accessed February 23, 2015
    • CFTR project (USA) Available at: www.cftr2.org. Accessed February 23, 2015
  • 5
    • 0037135779 scopus 로고    scopus 로고
    • Bronchiectasis in indigenous children in remote Australian communities
    • Working Group on Indigenous Paediatric Respiratory Health
    • Chang A. B., Grimwood K., Mulholland E. K., Torzillo P. J.; Working Group on Indigenous Paediatric Respiratory Health. Bronchiectasis in indigenous children in remote Australian communities. Med J Aust: 2002; 177 4 200 204
    • (2002) Med J Aust , vol.177 , Issue.4 , pp. 200-204
    • Chang, A.B.1    Grimwood, K.2    Mulholland, E.K.3    Torzillo, P.J.4
  • 6
    • 0034091702 scopus 로고    scopus 로고
    • Bronchiectasis in Alaska Native children: Causes and clinical courses
    • Singleton R., Morris A., Redding G., et al. Bronchiectasis in Alaska Native children: causes and clinical courses. Pediatr Pulmonol: 2000; 29 3 182 187
    • (2000) Pediatr Pulmonol , vol.29 , Issue.3 , pp. 182-187
    • Singleton, R.1    Morris, A.2    Redding, G.3
  • 7
    • 0025982378 scopus 로고
    • Effects of human neutrophil elastase and Pseudomonas aeruginosa proteinases on human respiratory epithelium
    • Amitani R., Wilson R., Rutman A., et al. Effects of human neutrophil elastase and Pseudomonas aeruginosa proteinases on human respiratory epithelium. Am J Respir Cell Mol Biol: 1991; 4 1 26 32
    • (1991) Am J Respir Cell Mol Biol , vol.4 , Issue.1 , pp. 26-32
    • Amitani, R.1    Wilson, R.2    Rutman, A.3
  • 8
    • 40649087414 scopus 로고    scopus 로고
    • Mucosal inflammation in idiopathic bronchiectasis: Cellular and molecular mechanisms
    • Fuschillo S., De Felice A., Balzano G. Mucosal inflammation in idiopathic bronchiectasis: cellular and molecular mechanisms. Eur Respir J: 2008; 31 2 396 406
    • (2008) Eur Respir J , vol.31 , Issue.2 , pp. 396-406
    • Fuschillo, S.1    De Felice, A.2    Balzano, G.3
  • 9
    • 0031881432 scopus 로고    scopus 로고
    • Determinants of eosinophil cationic protein in nasal lavages in children
    • Wojnarowski C., Studnicka M., Kühr J., et al. Determinants of eosinophil cationic protein in nasal lavages in children. Clin Exp Allergy: 1998; 28 3 300 305
    • (1998) Clin Exp Allergy , vol.28 , Issue.3 , pp. 300-305
    • Wojnarowski, C.1    Studnicka, M.2    Kühr, J.3
  • 10
    • 84884331071 scopus 로고    scopus 로고
    • Mechanisms of airway remodeling
    • Hirota N., Martin J. G. Mechanisms of airway remodeling. Chest: 2013; 144 3 1026 1032
    • (2013) Chest , vol.144 , Issue.3 , pp. 1026-1032
    • Hirota, N.1    Martin, J.G.2
  • 12
    • 34250893256 scopus 로고    scopus 로고
    • Endobronchial biopsy in childhood
    • Colin A. A., Ali-Dinar T. Endobronchial biopsy in childhood. Chest: 2007; 131 6 1626 1627
    • (2007) Chest , vol.131 , Issue.6 , pp. 1626-1627
    • Colin, A.A.1    Ali-Dinar, T.2
  • 13
    • 0017198208 scopus 로고
    • The lung in cystic fibrosis. A quantitative study including prevalence of pathologic findings among different age groups
    • Bedrossian C. W., Greenberg S. D., Singer D. B., Hansen J. J., Rosenberg H. S. The lung in cystic fibrosis. A quantitative study including prevalence of pathologic findings among different age groups. Hum Pathol: 1976; 7 2 195 204
    • (1976) Hum Pathol , vol.7 , Issue.2 , pp. 195-204
    • Bedrossian, C.W.1    Greenberg, S.D.2    Singer, D.B.3    Hansen, J.J.4    Rosenberg, H.S.5
  • 15
    • 77953255282 scopus 로고    scopus 로고
    • Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis
    • Bienvenu T., Sermet-Gaudelus I., Burgel P. R., et al. Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis. Am J Respir Crit Care Med: 2010; 181 10 1078 1084
    • (2010) Am J Respir Crit Care Med , vol.181 , Issue.10 , pp. 1078-1084
    • Bienvenu, T.1    Sermet-Gaudelus, I.2    Burgel, P.R.3
  • 16
    • 84862770787 scopus 로고    scopus 로고
    • Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary disease
    • Gonska T., Choi P., Stephenson A., et al. Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary disease. Chest: 2012; 142 4 996 1004
    • (2012) Chest , vol.142 , Issue.4 , pp. 996-1004
    • Gonska, T.1    Choi, P.2    Stephenson, A.3
  • 17
    • 33749845468 scopus 로고    scopus 로고
    • Characterisation of the onset and presenting clinical features of adult bronchiectasis
    • King P. T., Holdsworth S. R., Freezer N. J., Villanueva E., Holmes P. W. Characterisation of the onset and presenting clinical features of adult bronchiectasis. Respir Med: 2006; 100 12 2183 2189
    • (2006) Respir Med , vol.100 , Issue.12 , pp. 2183-2189
    • King, P.T.1    Holdsworth, S.R.2    Freezer, N.J.3    Villanueva, E.4    Holmes, P.W.5
  • 18
    • 84893972760 scopus 로고    scopus 로고
    • Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis
    • Ooi C. Y., Dupuis A., Ellis L., et al. Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis? Thorax: 2014; 69 3 254 260
    • (2014) Thorax , vol.69 , Issue.3 , pp. 254-260
    • Ooi, C.Y.1    Dupuis, A.2    Ellis, L.3
  • 19
    • 0033773862 scopus 로고    scopus 로고
    • An investigation into causative factors in patients with bronchiectasis
    • 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
    • (2000) Am J Respir Crit Care Med , vol.162 , Issue.4 , pp. 1277-1284
    • Pasteur, M.C.1    Helliwell, S.M.2    Houghton, S.J.3
  • 20
    • 0028958565 scopus 로고
    • Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis
    • Pignatti P. F., Bombieri C., Marigo C., Benetazzo M., Luisetti M. Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis. Hum Mol Genet: 1995; 4 4 635 639
    • (1995) Hum Mol Genet , vol.4 , Issue.4 , pp. 635-639
    • Pignatti, P.F.1    Bombieri, C.2    Marigo, C.3    Benetazzo, M.4    Luisetti, M.5
  • 21
    • 77955283910 scopus 로고    scopus 로고
    • British Thoracic Society guideline for non-CF bronchiectasis
    • British Thoracic Society Bronchiectasis non-CF Guideline Group. 01
    • Pasteur M. C., Bilton D., Hill A. T.; British Thoracic Society Bronchiectasis non-CF Guideline Group. British Thoracic Society guideline for non-CF bronchiectasis. Thorax: 2010; 65 01 i1 i58
    • (2010) Thorax , vol.65 , pp. i1-i58
    • Pasteur, M.C.1    Bilton, D.2    Hill, A.T.3
  • 25
    • 79958069364 scopus 로고    scopus 로고
    • The airway microbiome in cystic fibrosis and implications for treatment
    • Zemanick E. T., Sagel S. D., Harris J. K. The airway microbiome in cystic fibrosis and implications for treatment. Curr Opin Pediatr: 2011; 23 3 319 324
    • (2011) Curr Opin Pediatr , vol.23 , Issue.3 , pp. 319-324
    • Zemanick, E.T.1    Sagel, S.D.2    Harris, J.K.3
  • 26
    • 78449278858 scopus 로고    scopus 로고
    • Respiratory bacterial pathogens in the nasopharynx and lower airways of Australian indigenous children with bronchiectasis
    • Hare K. M., Grimwood K., Leach A. J., et al. Respiratory bacterial pathogens in the nasopharynx and lower airways of Australian indigenous children with bronchiectasis. J Pediatr: 2010; 157 6 1001 1005
    • (2010) J Pediatr , vol.157 , Issue.6 , pp. 1001-1005
    • Hare, K.M.1    Grimwood, K.2    Leach, A.J.3
  • 27
    • 84857355367 scopus 로고    scopus 로고
    • Lower airway microbiology and cellularity in children with newly diagnosed non-CF bronchiectasis
    • Kapur N., Grimwood K., Masters I. B., Morris P. S., Chang A. B. Lower airway microbiology and cellularity in children with newly diagnosed non-CF bronchiectasis. Pediatr Pulmonol: 2012; 47 3 300 307
    • (2012) Pediatr Pulmonol , vol.47 , Issue.3 , pp. 300-307
    • Kapur, N.1    Grimwood, K.2    Masters, I.B.3    Morris, P.S.4    Chang, A.B.5
  • 28
    • 0036143373 scopus 로고    scopus 로고
    • Bacterial colonisation in patients with bronchiectasis: Microbiological pattern and risk factors
    • Angrill J., Agustí C., de Celis R., et al. Bacterial colonisation in patients with bronchiectasis: microbiological pattern and risk factors. Thorax: 2002; 57 1 15 19
    • (2002) Thorax , vol.57 , Issue.1 , pp. 15-19
    • Angrill, J.1    Agustí, C.2    De Celis, R.3
  • 29
    • 0036928877 scopus 로고    scopus 로고
    • Validation of the Hong Kong Chinese version of the St. George Respiratory Questionnaire in patients with bronchiectasis
    • Chan S. L., Chan-Yeung M. M., Ooi G. C., et al. Validation of the Hong Kong Chinese version of the St. George Respiratory Questionnaire in patients with bronchiectasis. Chest: 2002; 122 6 2030 2037
    • (2002) Chest , vol.122 , Issue.6 , pp. 2030-2037
    • Chan, S.L.1    Chan-Yeung, M.M.2    Ooi, G.C.3
  • 30
    • 0036335352 scopus 로고    scopus 로고
    • Clinical, laboratory findings and microbiologic characterization of bronchiectasis in Thai patients
    • Palwatwichai A., Chaoprasong C., Vattanathum A., Wongsa A., Jatakanon A. Clinical, laboratory findings and microbiologic characterization of bronchiectasis in Thai patients. Respirology: 2002; 7 1 63 66
    • (2002) Respirology , vol.7 , Issue.1 , pp. 63-66
    • Palwatwichai, A.1    Chaoprasong, C.2    Vattanathum, A.3    Wongsa, A.4    Jatakanon, A.5
  • 31
    • 84879963088 scopus 로고    scopus 로고
    • Clinical measures of disease in adult non-CF bronchiectasis correlate with airway microbiota composition
    • Rogers G. B., van der Gast C. J., Cuthbertson L., et al. Clinical measures of disease in adult non-CF bronchiectasis correlate with airway microbiota composition. Thorax: 2013; 68 8 731 737
    • (2013) Thorax , vol.68 , Issue.8 , pp. 731-737
    • Rogers, G.B.1    Van Der Gast, C.J.2    Cuthbertson, L.3
  • 32
    • 84877918651 scopus 로고    scopus 로고
    • Lung microbiota and bacterial abundance in patients with bronchiectasis when clinically stable and during exacerbation
    • Tunney M. M., Einarsson G. G., 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 1126
    • (2013) Am J Respir Crit Care Med , vol.187 , Issue.10 , pp. 1118-1126
    • Tunney, M.M.1    Einarsson, G.G.2    Wei, L.3
  • 33
    • 84903478837 scopus 로고    scopus 로고
    • A novel microbiota stratification system predicts future exacerbations in bronchiectasis
    • Rogers G. B., Zain N. M., Bruce K. D., et al. A novel microbiota stratification system predicts future exacerbations in bronchiectasis. Ann Am Thorac Soc: 2014; 11 4 496 503
    • (2014) Ann Am Thorac Soc , vol.11 , Issue.4 , pp. 496-503
    • Rogers, G.B.1    Zain, N.M.2    Bruce, K.D.3
  • 34
    • 0029761031 scopus 로고    scopus 로고
    • Lung function in bronchiectasis: The influence of Pseudomonas aeruginosa
    • Evans S. A., Turner S. M., Bosch B. J., Hardy C. C., Woodhead M. A. Lung function in bronchiectasis: the influence of Pseudomonas aeruginosa. Eur Respir J: 1996; 9 8 1601 1604
    • (1996) Eur Respir J , vol.9 , Issue.8 , pp. 1601-1604
    • Evans, S.A.1    Turner, S.M.2    Bosch, B.J.3    Hardy, C.C.4    Woodhead, M.A.5
  • 35
    • 0032253292 scopus 로고    scopus 로고
    • The effect of Pseudomonas aeruginosa infection on clinical parameters in steady-state bronchiectasis
    • Ho P. L., Chan K. N., Ip M. S., et al. The effect of Pseudomonas aeruginosa infection on clinical parameters in steady-state bronchiectasis. Chest: 1998; 114 6 1594 1598
    • (1998) Chest , vol.114 , Issue.6 , pp. 1594-1598
    • Ho, P.L.1    Chan, K.N.2    Ip, M.S.3
  • 36
    • 36348949002 scopus 로고    scopus 로고
    • Factors associated with lung function decline in adult patients with stable non-cystic fibrosis bronchiectasis
    • Martínez-García M. A., Soler-Cataluña J. J., Perpiñá-Tordera M., Román-Sánchez P., Soriano J. Factors associated with lung function decline in adult patients with stable non-cystic fibrosis bronchiectasis. Chest: 2007; 132 5 1565 1572
    • (2007) Chest , vol.132 , Issue.5 , pp. 1565-1572
    • Martínez-García, M.A.1    Soler-Cataluña, J.J.2    Perpiñá-Tordera, M.3    Román-Sánchez, P.4    Soriano, J.5
  • 37
    • 0030991452 scopus 로고    scopus 로고
    • Effects of airway infection by Pseudomonas aeruginosa: A computed tomographic study
    • Miszkiel K. A., Wells A. U., Rubens M. B., Cole P. J., Hansell D. M. Effects of airway infection by Pseudomonas aeruginosa: a computed tomographic study. Thorax: 1997; 52 3 260 264
    • (1997) Thorax , vol.52 , Issue.3 , pp. 260-264
    • Miszkiel, K.A.1    Wells, A.U.2    Rubens, M.B.3    Cole, P.J.4    Hansell, D.M.5
  • 38
    • 0030879813 scopus 로고    scopus 로고
    • Effect of sputum bacteriology on the quality of life of patients with bronchiectasis
    • Wilson C. B., Jones P. W., O'Leary C. J., Hansell D. M., Cole P. J., Wilson R. Effect of sputum bacteriology on the quality of life of patients with bronchiectasis. Eur Respir J: 1997; 10 8 1754 1760
    • (1997) Eur Respir J , vol.10 , Issue.8 , pp. 1754-1760
    • Wilson, C.B.1    Jones, P.W.2    O'Leary, C.J.3    Hansell, D.M.4    Cole, P.J.5    Wilson, R.6
  • 39
    • 84905644717 scopus 로고    scopus 로고
    • Inhaled antibiotics for stable non-cystic fibrosis bronchiectasis: A systematic review
    • Brodt A. M., Stovold E., Zhang L. Inhaled antibiotics for stable non-cystic fibrosis bronchiectasis: a systematic review. Eur Respir J: 2014; 44 2 382 393
    • (2014) Eur Respir J , vol.44 , Issue.2 , pp. 382-393
    • Brodt, A.M.1    Stovold, E.2    Zhang, L.3
  • 40
    • 79953284775 scopus 로고    scopus 로고
    • Inhaled antibiotics for long-term therapy in cystic fibrosis
    • Ryan G., Singh M., Dwan K. Inhaled antibiotics for long-term therapy in cystic fibrosis. Cochrane Database Syst Rev: 2011; 3 CD001021
    • (2011) Cochrane Database Syst Rev , Issue.3 , pp. CD001021
    • Ryan, G.1    Singh, M.2    Dwan, K.3
  • 41
    • 84923932616 scopus 로고    scopus 로고
    • Predominant pathogen competition and core microbiota divergence in chronic airway infection
    • Rogers G. B., van der Gast C. J., Serisier D. J. Predominant pathogen competition and core microbiota divergence in chronic airway infection. ISME J: 2015; 9 1 217 225
    • (2015) ISME J , vol.9 , Issue.1 , pp. 217-225
    • Rogers, G.B.1    Van Der Gast, C.J.2    Serisier, D.J.3
  • 42
    • 84866841728 scopus 로고    scopus 로고
    • The adult cystic fibrosis airway microbiota is stable over time and infection type, and highly resilient to antibiotic treatment of exacerbations
    • Fodor A. A., Klem E. R., Gilpin D. F., et al. The adult cystic fibrosis airway microbiota is stable over time and infection type, and highly resilient to antibiotic treatment of exacerbations. PLoS ONE: 2012; 7 9 e45001
    • (2012) PLoS ONE , vol.7 , Issue.9 , pp. e45001
    • Fodor, A.A.1    Klem, E.R.2    Gilpin, D.F.3
  • 43
    • 84907522276 scopus 로고    scopus 로고
    • Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics
    • Smith D. J., Badrick A. C., Zakrzewski M., et al. Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics. Eur Respir J: 2014; 44 4 922 930
    • (2014) Eur Respir J , vol.44 , Issue.4 , pp. 922-930
    • Smith, D.J.1    Badrick, A.C.2    Zakrzewski, M.3
  • 44
    • 84901602232 scopus 로고    scopus 로고
    • Emerging cystic fibrosis pathogens and the microbiome
    • 01
    • Mahenthiralingam E. Emerging cystic fibrosis pathogens and the microbiome. Paediatr Respir Rev: 2014; 15 01 13 15
    • (2014) Paediatr Respir Rev , vol.15 , pp. 13-15
    • Mahenthiralingam, E.1
  • 45
    • 42949105490 scopus 로고    scopus 로고
    • Detection of anaerobic bacteria in high numbers in sputum from patients with cystic fibrosis
    • Tunney M. M., Field T. R., Moriarty T. F., et al. Detection of anaerobic bacteria in high numbers in sputum from patients with cystic fibrosis. Am J Respir Crit Care Med: 2008; 177 9 995 1001
    • (2008) Am J Respir Crit Care Med , vol.177 , Issue.9 , pp. 995-1001
    • Tunney, M.M.1    Field, T.R.2    Moriarty, T.F.3
  • 46
    • 79959325084 scopus 로고    scopus 로고
    • Use of culture and molecular analysis to determine the effect of antibiotic treatment on microbial community diversity and abundance during exacerbation in patients with cystic fibrosis
    • Tunney M. M., Klem E. R., Fodor A. A., et al. Use of culture and molecular analysis to determine the effect of antibiotic treatment on microbial community diversity and abundance during exacerbation in patients with cystic fibrosis. Thorax: 2011; 66 7 579 584
    • (2011) Thorax , vol.66 , Issue.7 , pp. 579-584
    • Tunney, M.M.1    Klem, E.R.2    Fodor, A.A.3
  • 47
    • 79959306147 scopus 로고    scopus 로고
    • Anaerobic bacteria in cystic fibrosis: Pathogens or harmless commensals
    • Jones A. M. Anaerobic bacteria in cystic fibrosis: pathogens or harmless commensals? Thorax: 2011; 66 7 558 559
    • (2011) Thorax , vol.66 , Issue.7 , pp. 558-559
    • Jones, A.M.1
  • 48
    • 84907060662 scopus 로고    scopus 로고
    • Three clinically distinct chronic pediatric airway infections share a common core microbiota
    • van der Gast C. J., Cuthbertson L., Rogers G. B., et al. Three clinically distinct chronic pediatric airway infections share a common core microbiota. Ann Am Thorac Soc: 2014; 11 7 1039 1048
    • (2014) Ann Am Thorac Soc , vol.11 , Issue.7 , pp. 1039-1048
    • Van Der Gast, C.J.1    Cuthbertson, L.2    Rogers, G.B.3
  • 50
    • 78650181025 scopus 로고    scopus 로고
    • Pseudomonas aeruginosa biofilms in cystic fibrosis
    • Hoiby N., Ciofu O., Bjarnsholt T. Pseudomonas aeruginosa biofilms in cystic fibrosis. Future Microbiol: 2010; 5 11 1663 1674
    • (2010) Future Microbiol , vol.5 , Issue.11 , pp. 1663-1674
    • Hoiby, N.1    Ciofu, O.2    Bjarnsholt, T.3
  • 51
    • 33747065797 scopus 로고    scopus 로고
    • Switch from planktonic to sessile life: A major event in pneumococcal pathogenesis
    • Oggioni M. R., Trappetti C., Kadioglu A., et al. Switch from planktonic to sessile life: a major event in pneumococcal pathogenesis. Mol Microbiol: 2006; 61 5 1196 1210
    • (2006) Mol Microbiol , vol.61 , Issue.5 , pp. 1196-1210
    • Oggioni, M.R.1    Trappetti, C.2    Kadioglu, A.3
  • 52
    • 33745757955 scopus 로고    scopus 로고
    • Haemophilus influenzae forms biofilms on airway epithelia: Implications in cystic fibrosis
    • Starner T. D., Zhang N., Kim G., Apicella M. A., McCray P. B. Jr. Haemophilus influenzae forms biofilms on airway epithelia: implications in cystic fibrosis. Am J Respir Crit Care Med: 2006; 174 2 213 220
    • (2006) Am J Respir Crit Care Med , vol.174 , Issue.2 , pp. 213-220
    • Starner, T.D.1    Zhang, N.2    Kim, G.3    Apicella, M.A.4    Mccray, P.B.5
  • 54
    • 0028232830 scopus 로고
    • Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator
    • Poulsen J. H., Fischer H., Illek B., Machen T. E. Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator. Proc Natl Acad Sci U S A: 1994; 91 12 5340 5344
    • (1994) Proc Natl Acad Sci U S A , vol.91 , Issue.12 , pp. 5340-5344
    • Poulsen, J.H.1    Fischer, H.2    Illek, B.3    Machen, T.E.4
  • 55
    • 34748845101 scopus 로고    scopus 로고
    • Effect of pH on the antimicrobial susceptibility of planktonic and biofilm-grown clinical Pseudomonas aeruginosa isolates
    • Moriarty T. F., Elborn J. S., Tunney M. M. Effect of pH on the antimicrobial susceptibility of planktonic and biofilm-grown clinical Pseudomonas aeruginosa isolates. Br J Biomed Sci: 2007; 64 3 101 104
    • (2007) Br J Biomed Sci , vol.64 , Issue.3 , pp. 101-104
    • Moriarty, T.F.1    Elborn, J.S.2    Tunney, M.M.3
  • 56
    • 0036167851 scopus 로고    scopus 로고
    • Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients
    • Worlitzsch D., Tarran R., Ulrich M., et al. Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients. J Clin Invest: 2002; 109 3 317 325
    • (2002) J Clin Invest , vol.109 , Issue.3 , pp. 317-325
    • Worlitzsch, D.1    Tarran, R.2    Ulrich, M.3
  • 57
    • 27944440475 scopus 로고    scopus 로고
    • Effect of oxygen limitation on the in vitro antimicrobial susceptibility of clinical isolates of Pseudomonas aeruginosa grown planktonically and as biofilms
    • Field T. R., White A., Elborn J. S., Tunney M. M. Effect of oxygen limitation on the in vitro antimicrobial susceptibility of clinical isolates of Pseudomonas aeruginosa grown planktonically and as biofilms. Eur J Clin Microbiol Infect Dis: 2005; 24 10 677 687
    • (2005) Eur J Clin Microbiol Infect Dis , vol.24 , Issue.10 , pp. 677-687
    • Field, T.R.1    White, A.2    Elborn, J.S.3    Tunney, M.M.4
  • 58
    • 26944461986 scopus 로고    scopus 로고
    • Antibiotic susceptabilities of Pseudomonas aeruginosa isolates derived from patients with cystic fibrosis under aerobic, anaerobic, and biofilm conditions
    • Hill D., Rose B., Pajkos A., et al. Antibiotic susceptabilities of Pseudomonas aeruginosa isolates derived from patients with cystic fibrosis under aerobic, anaerobic, and biofilm conditions. J Clin Microbiol: 2005; 43 10 5085 5090
    • (2005) J Clin Microbiol , vol.43 , Issue.10 , pp. 5085-5090
    • Hill, D.1    Rose, B.2    Pajkos, A.3
  • 59
    • 84869120178 scopus 로고    scopus 로고
    • Treatment of lung infection in patients with cystic fibrosis: Current and future strategies
    • Consensus Study Group
    • Döring G., Flume P., Heijerman H., Elborn J. S.; Consensus Study Group. Treatment of lung infection in patients with cystic fibrosis: current and future strategies. J Cyst Fibros: 2012; 11 6 461 479
    • (2012) J Cyst Fibros , vol.11 , Issue.6 , pp. 461-479
    • Döring, G.1    Flume, P.2    Heijerman, H.3    Elborn, J.S.4
  • 60
    • 84896729978 scopus 로고    scopus 로고
    • Emerging drugs for cystic fibrosis
    • Amin R., Ratjen F. Emerging drugs for cystic fibrosis. Expert Opin Emerg Drugs: 2014; 19 1 143 155
    • (2014) Expert Opin Emerg Drugs , vol.19 , Issue.1 , pp. 143-155
    • Amin, R.1    Ratjen, F.2
  • 61
    • 84897115508 scopus 로고    scopus 로고
    • Inhaled aztreonam for chronic Burkholderia infection in cystic fibrosis: A placebo-controlled trial
    • Tullis D. E., Burns J. L., Retsch-Bogart G. Z., et al. Inhaled aztreonam for chronic Burkholderia infection in cystic fibrosis: a placebo-controlled trial. J Cyst Fibros: 2014; 13 3 296 305
    • (2014) J Cyst Fibros , vol.13 , Issue.3 , pp. 296-305
    • Tullis, D.E.1    Burns, J.L.2    Retsch-Bogart, G.Z.3
  • 62
    • 0027287651 scopus 로고
    • Efficacy of aerosolized tobramycin in patients with cystic fibrosis
    • Ramsey B. W., Dorkin H. L., Eisenberg J. D., et al. Efficacy of aerosolized tobramycin in patients with cystic fibrosis. N Engl J Med: 1993; 328 24 1740 1746
    • (1993) N Engl J Med , vol.328 , Issue.24 , pp. 1740-1746
    • Ramsey, B.W.1    Dorkin, H.L.2    Eisenberg, J.D.3
  • 63
    • 0033531143 scopus 로고    scopus 로고
    • Intermittent administration of inhaled tobramycin in patients with cystic fibrosis
    • Cystic Fibrosis Inhaled Tobramycin Study Group
    • Ramsey B. W., Pepe M. S., Quan J. M., et al. Cystic Fibrosis Inhaled Tobramycin Study Group. Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. N Engl J Med: 1999; 340 1 23 30
    • (1999) N Engl J Med , vol.340 , Issue.1 , pp. 23-30
    • Ramsey, B.W.1    Pepe, M.S.2    Quan, J.M.3
  • 64
    • 0036157901 scopus 로고    scopus 로고
    • Long-term benefits of inhaled tobramycin in adolescent patients with cystic fibrosis
    • Moss R. B. Long-term benefits of inhaled tobramycin in adolescent patients with cystic fibrosis. Chest: 2002; 121 1 55 63
    • (2002) Chest , vol.121 , Issue.1 , pp. 55-63
    • Moss, R.B.1
  • 65
    • 4544269731 scopus 로고    scopus 로고
    • Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung disease
    • Murphy T. D., Anbar R. D., Lester L. A., et al. Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung disease. Pediatr Pulmonol: 2004; 38 4 314 320
    • (2004) Pediatr Pulmonol , vol.38 , Issue.4 , pp. 314-320
    • Murphy, T.D.1    Anbar, R.D.2    Lester, L.A.3
  • 66
    • 79951840468 scopus 로고    scopus 로고
    • Tobramycin inhalation powder for P. Aeruginosa infection in cystic fibrosis: The EVOLVE trial
    • Konstan M. W., Geller D. E., Minić P., Brockhaus F., Zhang J., Angyalosi G. Tobramycin inhalation powder for P. aeruginosa infection in cystic fibrosis: the EVOLVE trial. Pediatr Pulmonol: 2011; 46 3 230 238
    • (2011) Pediatr Pulmonol , vol.46 , Issue.3 , pp. 230-238
    • Konstan, M.W.1    Geller, D.E.2    Minić, P.3    Brockhaus, F.4    Zhang, J.5    Angyalosi, G.6
  • 68
    • 78449294500 scopus 로고    scopus 로고
    • An 18-month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in cystic fibrosis
    • Oermann C. M., Retsch-Bogart G. Z., Quittner A. L., et al. An 18-month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in cystic fibrosis. Pediatr Pulmonol: 2010; 45 11 1121 1134
    • (2010) Pediatr Pulmonol , vol.45 , Issue.11 , pp. 1121-1134
    • Oermann, C.M.1    Retsch-Bogart, G.Z.2    Quittner, A.L.3
  • 69
    • 65949124667 scopus 로고    scopus 로고
    • Efficacy and safety of inhaled aztreonam lysine for airway pseudomonas in cystic fibrosis
    • Retsch-Bogart G. Z., Quittner A. L., Gibson R. L., et al. Efficacy and safety of inhaled aztreonam lysine for airway pseudomonas in cystic fibrosis. Chest: 2009; 135 5 1223 1232
    • (2009) Chest , vol.135 , Issue.5 , pp. 1223-1232
    • Retsch-Bogart, G.Z.1    Quittner, A.L.2    Gibson, R.L.3
  • 70
    • 79958295843 scopus 로고    scopus 로고
    • Aztreonam for inhalation solution (AZLI) in patients with cystic fibrosis, mild lung impairment, and P. Aeruginosa
    • Wainwright C. E., Quittner A. L., Geller D. E., et al. Aztreonam for inhalation solution (AZLI) in patients with cystic fibrosis, mild lung impairment, and P. aeruginosa. J Cyst Fibros: 2011; 10 4 234 242
    • (2011) J Cyst Fibros , vol.10 , Issue.4 , pp. 234-242
    • Wainwright, C.E.1    Quittner, A.L.2    Geller, D.E.3
  • 71
    • 0023265976 scopus 로고
    • Colistin inhalation therapy in cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infection
    • Jensen T., Pedersen S. S., Garne S., Heilmann C., Hoiby N., Koch C. Colistin inhalation therapy in cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infection. J Antimicrob Chemother: 1987; 19 6 831 838
    • (1987) J Antimicrob Chemother , vol.19 , Issue.6 , pp. 831-838
    • Jensen, T.1    Pedersen, S.S.2    Garne, S.3    Heilmann, C.4    Hoiby, N.5    Koch, C.6
  • 72
    • 0036736583 scopus 로고    scopus 로고
    • A randomised clinical trial of nebulised tobramycin or colistin in cystic fibrosis
    • Hodson M. E., Gallagher C. G., Govan J. R. A randomised clinical trial of nebulised tobramycin or colistin in cystic fibrosis. Eur Respir J: 2002; 20 3 658 664
    • (2002) Eur Respir J , vol.20 , Issue.3 , pp. 658-664
    • Hodson, M.E.1    Gallagher, C.G.2    Govan, J.R.3
  • 73
    • 84875215401 scopus 로고    scopus 로고
    • Safety, efficacy and convenience of colistimethate sodium dry powder for inhalation (Colobreathe DPI) in patients with cystic fibrosis: A randomised study
    • Freedom Study Group
    • Schuster A., Haliburn C., Döring G., Goldman M. H.; Freedom Study Group. Safety, efficacy and convenience of colistimethate sodium dry powder for inhalation (Colobreathe DPI) in patients with cystic fibrosis: a randomised study. Thorax: 2013; 68 4 344 350
    • (2013) Thorax , vol.68 , Issue.4 , pp. 344-350
    • Schuster, A.1    Haliburn, C.2    Döring, G.3    Goldman, M.H.4
  • 74
    • 84875842391 scopus 로고    scopus 로고
    • Inhaled aztreonam lysine vs. Inhaled tobramycin in cystic fibrosis: A comparative efficacy trial
    • AZLI Active Comparator Study Group
    • Assael B. M., Pressler T., Bilton D., et al. AZLI Active Comparator Study Group. Inhaled aztreonam lysine vs. inhaled tobramycin in cystic fibrosis: a comparative efficacy trial. J Cyst Fibros: 2013; 12 2 130 140
    • (2013) J Cyst Fibros , vol.12 , Issue.2 , pp. 130-140
    • Assael, B.M.1    Pressler, T.2    Bilton, D.3
  • 75
    • 0019511799 scopus 로고
    • Aerosol carbenicillin and gentamicin treatment of Pseudomonas aeruginosa infection in patients with cystic fibrosis
    • Hodson M. E., Penketh A. R., Batten J. C. Aerosol carbenicillin and gentamicin treatment of Pseudomonas aeruginosa infection in patients with cystic fibrosis. Lancet: 1981; 2 8256 1137 1139
    • (1981) Lancet , vol.2 , Issue.8256 , pp. 1137-1139
    • Hodson, M.E.1    Penketh, A.R.2    Batten, J.C.3
  • 76
    • 0024331219 scopus 로고
    • Long-term effects of inhaled tobramycin in patients with cystic fibrosis colonized with Pseudomonas aeruginosa
    • MacLusky I. B., Gold R., Corey M., Levison H. Long-term effects of inhaled tobramycin in patients with cystic fibrosis colonized with Pseudomonas aeruginosa. Pediatr Pulmonol: 1989; 7 1 42 48
    • (1989) Pediatr Pulmonol , vol.7 , Issue.1 , pp. 42-48
    • Maclusky, I.B.1    Gold, R.2    Corey, M.3    Levison, H.4
  • 77
    • 0019987826 scopus 로고
    • Antibiotic prophylaxis in cystic fibrosis: Inhaled cephaloridine as an adjunct to oral cloxacillin
    • Nolan G., Moivor P., Levison H., Fleming P. C., Corey M., Gold R. Antibiotic prophylaxis in cystic fibrosis: inhaled cephaloridine as an adjunct to oral cloxacillin. J Pediatr: 1982; 101 4 626 630
    • (1982) J Pediatr , vol.101 , Issue.4 , pp. 626-630
    • Nolan, G.1    Moivor, P.2    Levison, H.3    Fleming, P.C.4    Corey, M.5    Gold, R.6
  • 78
    • 2642712510 scopus 로고    scopus 로고
    • Placebo-controlled, double-blind, randomized study of aerosolized tobramycin for early treatment of Pseudomonas aeruginosa colonization in cystic fibrosis
    • Wiesemann H. G., Steinkamp G., Ratjen F., et al. Placebo-controlled, double-blind, randomized study of aerosolized tobramycin for early treatment of Pseudomonas aeruginosa colonization in cystic fibrosis. Pediatr Pulmonol: 1998; 25 2 88 92
    • (1998) Pediatr Pulmonol , vol.25 , Issue.2 , pp. 88-92
    • Wiesemann, H.G.1    Steinkamp, G.2    Ratjen, F.3
  • 79
    • 0024790626 scopus 로고
    • Safety of aerosol tobramycin administration for 3 months to patients with cystic fibrosis
    • Smith A. L., Ramsey B. W., Hedges D. L., et al. Safety of aerosol tobramycin administration for 3 months to patients with cystic fibrosis. Pediatr Pulmonol: 1989; 7 4 265 271
    • (1989) Pediatr Pulmonol , vol.7 , Issue.4 , pp. 265-271
    • Smith, A.L.1    Ramsey, B.W.2    Hedges, D.L.3
  • 80
    • 0035989385 scopus 로고    scopus 로고
    • Bronchial reactions to the inhalation of high-dose tobramycin in cystic fibrosis
    • Nikolaizik W. H., Trociewicz K., Ratjen F. Bronchial reactions to the inhalation of high-dose tobramycin in cystic fibrosis. Eur Respir J: 2002; 20 1 122 126
    • (2002) Eur Respir J , vol.20 , Issue.1 , pp. 122-126
    • Nikolaizik, W.H.1    Trociewicz, K.2    Ratjen, F.3
  • 81
    • 0036382644 scopus 로고    scopus 로고
    • Evaluation of bronchial constriction in children with cystic fibrosis after inhaling two different preparations of tobramycin
    • Alothman G. A., Alsaadi M. M., Ho B. L., et al. Evaluation of bronchial constriction in children with cystic fibrosis after inhaling two different preparations of tobramycin. Chest: 2002; 122 3 930 934
    • (2002) Chest , vol.122 , Issue.3 , pp. 930-934
    • Alothman, G.A.1    Alsaadi, M.M.2    Ho, B.L.3
  • 82
    • 0032968947 scopus 로고    scopus 로고
    • Effect of chronic intermittent administration of inhaled tobramycin on respiratory microbial flora in patients with cystic fibrosis
    • Burns J. L., Van Dalfsen J. M., Shawar R. M., et al. Effect of chronic intermittent administration of inhaled tobramycin on respiratory microbial flora in patients with cystic fibrosis. J Infect Dis: 1999; 179 5 1190 1196
    • (1999) J Infect Dis , vol.179 , Issue.5 , pp. 1190-1196
    • Burns, J.L.1    Van Dalfsen, J.M.2    Shawar, R.M.3
  • 83
    • 78651412529 scopus 로고    scopus 로고
    • Safety, efficacy and convenience of tobramycin inhalation powder in cystic fibrosis patients: The EAGER trial
    • Konstan M. W., Flume P. A., Kappler M., et al. Safety, efficacy and convenience of tobramycin inhalation powder in cystic fibrosis patients: The EAGER trial. J Cyst Fibros: 2011; 10 1 54 61
    • (2011) J Cyst Fibros , vol.10 , Issue.1 , pp. 54-61
    • Konstan, M.W.1    Flume, P.A.2    Kappler, M.3
  • 84
    • 0016611606 scopus 로고
    • Cystic fibrosis: Comparison of two mucolytic drugs for inhalation treatment (acetylcysteine and arginine hydrochloride)
    • Dietzsch H. J., Gottschalk B., Heyne K., Leupoid W., Wunderlich P. Cystic fibrosis: comparison of two mucolytic drugs for inhalation treatment (acetylcysteine and arginine hydrochloride). Pediatrics: 1975; 55 1 96 100
    • (1975) Pediatrics , vol.55 , Issue.1 , pp. 96-100
    • Dietzsch, H.J.1    Gottschalk, B.2    Heyne, K.3    Leupoid, W.4    Wunderlich, P.5
  • 85
    • 33745686502 scopus 로고    scopus 로고
    • Microbiology, safety, and pharmacokinetics of aztreonam lysinate for inhalation in patients with cystic fibrosis
    • Gibson R. L., Retsch-Bogart G. Z., Oermann C., et al. Microbiology, safety, and pharmacokinetics of aztreonam lysinate for inhalation in patients with cystic fibrosis. Pediatr Pulmonol: 2006; 41 7 656 665
    • (2006) Pediatr Pulmonol , vol.41 , Issue.7 , pp. 656-665
    • Gibson, R.L.1    Retsch-Bogart, G.Z.2    Oermann, C.3
  • 86
    • 38349058630 scopus 로고    scopus 로고
    • A phase 2 study of aztreonam lysine for inhalation to treat patients with cystic fibrosis and Pseudomonas aeruginosa infection
    • AZLI Phase II Study Group
    • Retsch-Bogart G. Z., Burns J. L., Otto K. L., et al. AZLI Phase II Study Group. A phase 2 study of aztreonam lysine for inhalation to treat patients with cystic fibrosis and Pseudomonas aeruginosa infection. Pediatr Pulmonol: 2008; 43 1 47 58
    • (2008) Pediatr Pulmonol , vol.43 , Issue.1 , pp. 47-58
    • Retsch-Bogart, G.Z.1    Burns, J.L.2    Otto, K.L.3
  • 87
    • 0023243958 scopus 로고
    • Aztreonam for cystic fibrosis patients who are hypersensitive to other beta-lactams
    • Jensen T., Koch C., Pedersen S. S., Hoiby N. Aztreonam for cystic fibrosis patients who are hypersensitive to other beta-lactams. Lancet: 1987; 1 8545 1319 1320
    • (1987) Lancet , vol.1 , Issue.8545 , pp. 1319-1320
    • Jensen, T.1    Koch, C.2    Pedersen, S.S.3    Hoiby, N.4
  • 89
    • 84878016233 scopus 로고    scopus 로고
    • Aztreonam for inhalation solution, challenges to drug approval and integration into CF care
    • Goss C. H., Bell S. C. Aztreonam for inhalation solution, challenges to drug approval and integration into CF care. J Cyst Fibros: 2013; 12 2 99 101
    • (2013) J Cyst Fibros , vol.12 , Issue.2 , pp. 99-101
    • Goss, C.H.1    Bell, S.C.2
  • 90
    • 84875829440 scopus 로고    scopus 로고
    • Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health
    • Pulmonary Clinical Practice Guidelines Committee
    • Mogayzel P. J. Jr, Naureckas E. T., Robinson K. A., et al. Pulmonary Clinical Practice Guidelines Committee. Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health. Am J Respir Crit Care Med: 2013; 187 7 680 689
    • (2013) Am J Respir Crit Care Med , vol.187 , Issue.7 , pp. 680-689
    • Mogayzel, P.J.1    Naureckas, E.T.2    Robinson, K.A.3
  • 91
    • 84901006449 scopus 로고    scopus 로고
    • European Cystic Fibrosis Society Standards of Care: Best Practice guidelines
    • 01
    • Smyth A. R., Bell S. C., Bojcin S., et al. European Cystic Fibrosis Society Standards of Care: Best Practice guidelines. J Cyst Fibros: 2014; 13 01 S23 S42
    • (2014) J Cyst Fibros , vol.13 , pp. S23-S42
    • Smyth, A.R.1    Bell, S.C.2    Bojcin, S.3
  • 92
    • 0025868478 scopus 로고
    • Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment
    • Valerius N. H., Koch C., Hoiby N. Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment. Lancet: 1991; 338 8769 725 726
    • (1991) Lancet , vol.338 , Issue.8769 , pp. 725-726
    • Valerius, N.H.1    Koch, C.2    Hoiby, N.3
  • 93
    • 84922237712 scopus 로고    scopus 로고
    • Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis
    • Langton Hewer S. C., Smyth A. R. Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis. Cochrane Database Syst Rev: 2014; 11 CD004197
    • (2014) Cochrane Database Syst Rev , vol.11 , pp. CD004197
    • Langton Hewer, S.C.1    Smyth, A.R.2
  • 94
    • 84918771958 scopus 로고    scopus 로고
    • Open label study of inhaled aztreonam for Pseudomonas eradication in children with cystic fibrosis: The ALPINE study
    • ALPINE study investigators
    • Tiddens H. A., De Boeck K., Clancy J. P., et al. ALPINE study investigators. Open label study of inhaled aztreonam for Pseudomonas eradication in children with cystic fibrosis: The ALPINE study. J Cyst Fibros: 2015; 14 1 111 119
    • (2015) J Cyst Fibros , vol.14 , Issue.1 , pp. 111-119
    • Tiddens, H.A.1    De Boeck, K.2    Clancy, J.P.3
  • 95
    • 84874120960 scopus 로고    scopus 로고
    • Inhaled antibiotics for pulmonary exacerbations in cystic fibrosis
    • Ryan G., Jahnke N., Remmington T. Inhaled antibiotics for pulmonary exacerbations in cystic fibrosis. Cochrane Database Syst Rev: 2012; 12 CD008319
    • (2012) Cochrane Database Syst Rev , vol.12 , pp. CD008319
    • Ryan, G.1    Jahnke, N.2    Remmington, T.3
  • 96
    • 41149105955 scopus 로고    scopus 로고
    • Biofilm penetration, triggered release and in vivo activity of inhaled liposomal amikacin in chronic Pseudomonas aeruginosa lung infections
    • Meers P., Neville M., Malinin V., et al. Biofilm penetration, triggered release and in vivo activity of inhaled liposomal amikacin in chronic Pseudomonas aeruginosa lung infections. J Antimicrob Chemother: 2008; 61 4 859 868
    • (2008) J Antimicrob Chemother , vol.61 , Issue.4 , pp. 859-868
    • Meers, P.1    Neville, M.2    Malinin, V.3
  • 97
    • 84881542878 scopus 로고    scopus 로고
    • Phase II studies of nebulised Arikace in CF patients with Pseudomonas aeruginosa infection
    • Arikace Study Group
    • Clancy J. P., Dupont L., Konstan M. W., et al. Arikace Study Group. Phase II studies of nebulised Arikace in CF patients with Pseudomonas aeruginosa infection. Thorax: 2013; 68 9 818 825
    • (2013) Thorax , vol.68 , Issue.9 , pp. 818-825
    • Clancy, J.P.1    Dupont, L.2    Konstan, M.W.3
  • 98
    • 79956336460 scopus 로고    scopus 로고
    • Pharmacokinetics and safety of MP-376 (levofloxacin inhalation solution) in cystic fibrosis subjects
    • Geller D. E., Flume P. A., Griffith D. C., et al. Pharmacokinetics and safety of MP-376 (levofloxacin inhalation solution) in cystic fibrosis subjects. Antimicrob Agents Chemother: 2011; 55 6 2636 2640
    • (2011) Antimicrob Agents Chemother , vol.55 , Issue.6 , pp. 2636-2640
    • Geller, D.E.1    Flume, P.A.2    Griffith, D.C.3
  • 99
    • 79957942626 scopus 로고    scopus 로고
    • Levofloxacin inhalation solution (MP-376) in patients with cystic fibrosis with Pseudomonas aeruginosa
    • Mpex 204 Study Group
    • Geller D. E., Flume P. A., Staab D., Fischer R., Loutit J. S., Conrad D. J.; Mpex 204 Study Group. Levofloxacin inhalation solution (MP-376) in patients with cystic fibrosis with Pseudomonas aeruginosa. Am J Respir Crit Care Med: 2011; 183 11 1510 1516
    • (2011) Am J Respir Crit Care Med , vol.183 , Issue.11 , pp. 1510-1516
    • Geller, D.E.1    Flume, P.A.2    Staab, D.3    Fischer, R.4    Loutit, J.S.5    Conrad, D.J.6
  • 100
    • 84856010859 scopus 로고    scopus 로고
    • Fosfomycin/tobramycin for inhalation in patients with cystic fibrosis with pseudomonas airway infection
    • Phase 2 FTI Study Group
    • Trapnell B. C., McColley S. A., Kissner D. G., et al. Phase 2 FTI Study Group. Fosfomycin/tobramycin for inhalation in patients with cystic fibrosis with pseudomonas airway infection. Am J Respir Crit Care Med: 2012; 185 2 171 178
    • (2012) Am J Respir Crit Care Med , vol.185 , Issue.2 , pp. 171-178
    • Trapnell, B.C.1    McColley, S.A.2    Kissner, D.G.3
  • 101
    • 84907046532 scopus 로고    scopus 로고
    • Antimicrobial treatment of non-cystic fibrosis bronchiectasis
    • Grimwood K., Bell S. C., Chang A. B. Antimicrobial treatment of non-cystic fibrosis bronchiectasis. Expert Rev Anti Infect Ther: 2014; 12 10 1277 1296
    • (2014) Expert Rev Anti Infect Ther , vol.12 , Issue.10 , pp. 1277-1296
    • Grimwood, K.1    Bell, S.C.2    Chang, A.B.3
  • 102
    • 84926318577 scopus 로고    scopus 로고
    • TR02-107 trial report. Available from
    • Insmed, Inc TR02-107 trial report. Available from: www.insmed.com/pdf/Pub9%209-13-09.pdf
  • 103
    • 0033841109 scopus 로고    scopus 로고
    • Tobramycin solution for inhalation reduces sputum Pseudomonas aeruginosa density in bronchiectasis
    • Barker A. F., Couch L., Fiel S. B., et al. Tobramycin solution for inhalation reduces sputum Pseudomonas aeruginosa density in bronchiectasis. Am J Respir Crit Care Med: 2000; 162 2 Pt 1 481 485
    • (2000) Am J Respir Crit Care Med , vol.162 , Issue.2 , pp. 481-485
    • Barker, A.F.1    Couch, L.2    Fiel, S.B.3
  • 104
    • 11144228397 scopus 로고    scopus 로고
    • Inhaled tobramycin in non-cystic fibrosis patients with bronchiectasis and chronic bronchial infection with Pseudomonas aeruginosa
    • Drobnic M. E., Suñé P., Montoro J. B., Ferrer A., Orriols R. Inhaled tobramycin in non-cystic fibrosis patients with bronchiectasis and chronic bronchial infection with Pseudomonas aeruginosa. Ann Pharmacother: 2005; 39 1 39 44
    • (2005) Ann Pharmacother , vol.39 , Issue.1 , pp. 39-44
    • Drobnic, M.E.1    Suñé, P.2    Montoro, J.B.3    Ferrer, A.4    Orriols, R.5
  • 105
    • 79951824943 scopus 로고    scopus 로고
    • A randomized controlled trial of nebulized gentamicin in non-cystic fibrosis bronchiectasis
    • Murray M. P., Govan J. R., Doherty C. J., et al. A randomized controlled trial of nebulized gentamicin in non-cystic fibrosis bronchiectasis. Am J Respir Crit Care Med: 2011; 183 4 491 499
    • (2011) Am J Respir Crit Care Med , vol.183 , Issue.4 , pp. 491-499
    • Murray, M.P.1    Govan, J.R.2    Doherty, C.J.3
  • 106
    • 84877093743 scopus 로고    scopus 로고
    • Ciprofloxacin dry powder for inhalation in non-cystic fibrosis bronchiectasis: A phase II randomised study
    • Wilson R., Welte T., Polverino E., et al. Ciprofloxacin dry powder for inhalation in non-cystic fibrosis bronchiectasis: a phase II randomised study. Eur Respir J: 2013; 41 5 1107 1115
    • (2013) Eur Respir J , vol.41 , Issue.5 , pp. 1107-1115
    • Wilson, R.1    Welte, T.2    Polverino, E.3
  • 107
    • 84881556337 scopus 로고    scopus 로고
    • Inhaled, dual release liposomal ciprofloxacin in non-cystic fibrosis bronchiectasis (ORBIT-2): A randomised, double-blind, placebo-controlled trial
    • ORBIT-2 investigators
    • Serisier D. J., Bilton D., De Soyza A., et al. ORBIT-2 investigators. Inhaled, dual release liposomal ciprofloxacin in non-cystic fibrosis bronchiectasis (ORBIT-2): a randomised, double-blind, placebo-controlled trial. Thorax: 2013; 68 9 812 817
    • (2013) Thorax , vol.68 , Issue.9 , pp. 812-817
    • Serisier, D.J.1    Bilton, D.2    De Soyza, A.3
  • 108
    • 84898994995 scopus 로고    scopus 로고
    • Inhaled colistin in patients with bronchiectasis and chronic Pseudomonas aeruginosa infection
    • Haworth C. S., Foweraker J. E., Wilkinson P., Kenyon R. F., Bilton D. Inhaled colistin in patients with bronchiectasis and chronic Pseudomonas aeruginosa infection. Am J Respir Crit Care Med: 2014; 189 8 975 982
    • (2014) Am J Respir Crit Care Med , vol.189 , Issue.8 , pp. 975-982
    • Haworth, C.S.1    Foweraker, J.E.2    Wilkinson, P.3    Kenyon, R.F.4    Bilton, D.5
  • 109
    • 84908070796 scopus 로고    scopus 로고
    • Aztreonam for inhalation solution in patients with non-cystic fibrosis bronchiectasis (AIR-BX1 and AIR-BX2): Two randomised double-blind, placebo-controlled phase 3 trials
    • Barker A. F., O'Donnell A. E., Flume P., et al. Aztreonam for inhalation solution in patients with non-cystic fibrosis bronchiectasis (AIR-BX1 and AIR-BX2): two randomised double-blind, placebo-controlled phase 3 trials. Lancet Respir Med: 2014; 2 9 738 749
    • (2014) Lancet Respir Med , vol.2 , Issue.9 , pp. 738-749
    • Barker, A.F.1    O'Donnell, A.E.2    Flume, P.3
  • 110
    • 0034821723 scopus 로고    scopus 로고
    • Treatment with tobramycin solution for inhalation in bronchiectasis patients with Pseudomonas aeruginosa
    • (3, Suppl)
    • Couch L. A. Treatment With tobramycin solution for inhalation in bronchiectasis patients with Pseudomonas aeruginosa. Chest: 2001; 120 (3, Suppl): 114S 117S
    • (2001) Chest , vol.120 , pp. 114S-117S
    • Couch, L.A.1
  • 111
    • 84982686523 scopus 로고    scopus 로고
    • Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand: TSANZ guidelines
    • Chang A. B., Bell S. C., Torzillo P. J., et al. Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand: TSANZ guidelines. Med J Aust: 2015; 202 1 21 23
    • (2015) Med J Aust , vol.202 , Issue.1 , pp. 21-23
    • Chang, A.B.1    Bell, S.C.2    Torzillo, P.J.3
  • 112
    • 82555194473 scopus 로고    scopus 로고
    • New guidelines for the management of adult lower respiratory tract infections
    • Woodhead M. New guidelines for the management of adult lower respiratory tract infections. Eur Respir J: 2011; 38 6 1250 1251
    • (2011) Eur Respir J , vol.38 , Issue.6 , pp. 1250-1251
    • Woodhead, M.1
  • 113
    • 33751243366 scopus 로고    scopus 로고
    • Addition of inhaled tobramycin to ciprofloxacin for acute exacerbations of Pseudomonas aeruginosa infection in adult bronchiectasis
    • Bilton D., Henig N., Morrissey B., Gotfried M. Addition of inhaled tobramycin to ciprofloxacin for acute exacerbations of Pseudomonas aeruginosa infection in adult bronchiectasis. Chest: 2006; 130 5 1503 1510
    • (2006) Chest , vol.130 , Issue.5 , pp. 1503-1510
    • Bilton, D.1    Henig, N.2    Morrissey, B.3    Gotfried, M.4
  • 114
    • 84878591147 scopus 로고    scopus 로고
    • Nebuliser systems for drug delivery in cystic fibrosis
    • Daniels T., Mills N., Whitaker P. Nebuliser systems for drug delivery in cystic fibrosis. Paediatr Respir Rev: 2013; 14 2 98 99
    • (2013) Paediatr Respir Rev , vol.14 , Issue.2 , pp. 98-99
    • Daniels, T.1    Mills, N.2    Whitaker, P.3
  • 115
    • 84900863789 scopus 로고    scopus 로고
    • [Inhaled treatments in cystic fibrosis: What's new in 2013?]
    • GRAM (Groupe aérosols et mucoviscidose de la Société française de mucoviscidose)
    • Dubus J. C., Bassinet L., Chedevergne F., et al. GRAM (Groupe aérosols et mucoviscidose de la Société française de mucoviscidose). [Inhaled treatments in cystic fibrosis: what's new in 2013?]. Rev Mal Respir: 2014; 31 4 336 346
    • (2014) Rev Mal Respir , vol.31 , Issue.4 , pp. 336-346
    • Dubus, J.C.1    Bassinet, L.2    Chedevergne, F.3
  • 116
    • 84908259448 scopus 로고    scopus 로고
    • Emerging inhalation aerosol devices and strategies: Where are we headed
    • Zhou Q. T., Tang P., Leung S. S., Chan J. G., Chan H. K. Emerging inhalation aerosol devices and strategies: where are we headed? Adv Drug Deliv Rev: 2014; 75 3 17
    • (2014) Adv Drug Deliv Rev , vol.75 , pp. 3-17
    • Zhou, Q.T.1    Tang, P.2    Leung, S.S.3    Chan, J.G.4    Chan, H.K.5
  • 118
    • 84927788695 scopus 로고    scopus 로고
    • Dry powder inhalers in cystic fibrosis: Same old drugs but different benefits
    • Uttley L., Tappenden P. Dry powder inhalers in cystic fibrosis: same old drugs but different benefits? Curr Opin Pulm Med: 2014; 20 6 607 612
    • (2014) Curr Opin Pulm Med , vol.20 , Issue.6 , pp. 607-612
    • Uttley, L.1    Tappenden, P.2
  • 119
    • 84894053561 scopus 로고    scopus 로고
    • The cost effectiveness of dry powder antibiotics for the treatment of Pseudomonas aeruginosa in patients with cystic fibrosis
    • Tappenden P., Harnan S., Uttley L., et al. The cost effectiveness of dry powder antibiotics for the treatment of Pseudomonas aeruginosa in patients with cystic fibrosis. Pharmacoeconomics: 2014; 32 2 159 172
    • (2014) Pharmacoeconomics , vol.32 , Issue.2 , pp. 159-172
    • Tappenden, P.1    Harnan, S.2    Uttley, L.3
  • 120
    • 84881479792 scopus 로고    scopus 로고
    • Isoniazid-gelatin conjugate microparticles containing rifampicin for the treatment of tuberculosis
    • Manca M. L., Cassano R., Valenti D., et al. Isoniazid-gelatin conjugate microparticles containing rifampicin for the treatment of tuberculosis. J Pharm Pharmacol: 2013; 65 9 1302 1311
    • (2013) J Pharm Pharmacol , vol.65 , Issue.9 , pp. 1302-1311
    • Manca, M.L.1    Cassano, R.2    Valenti, D.3
  • 121
    • 34547672749 scopus 로고    scopus 로고
    • Targeted delivery of magnetic aerosol droplets to the lung
    • Dames P., Gleich B., Flemmer A., et al. Targeted delivery of magnetic aerosol droplets to the lung. Nat Nanotechnol: 2007; 2 8 495 499
    • (2007) Nat Nanotechnol , vol.2 , Issue.8 , pp. 495-499
    • Dames, P.1    Gleich, B.2    Flemmer, A.3
  • 122
    • 38349149519 scopus 로고    scopus 로고
    • Nanomagnetosols: Magnetism opens up new perspectives for targeted aerosol delivery to the lung
    • Plank C. Nanomagnetosols: magnetism opens up new perspectives for targeted aerosol delivery to the lung. Trends Biotechnol: 2008; 26 2 59 63
    • (2008) Trends Biotechnol , vol.26 , Issue.2 , pp. 59-63
    • Plank, C.1
  • 123
    • 84919475713 scopus 로고    scopus 로고
    • Analysis of Changes in Diversity and Abundance of the Microbial Community in a Cystic Fibrosis Patient over a Multiyear Period
    • Stokell J. R., Gharaibeh R. Z., Hamp T. J., Zapata M. J., Fodor A. A., Steck T. R. Analysis of Changes in Diversity and Abundance of the Microbial Community in a Cystic Fibrosis Patient over a Multiyear Period. J Clin Microbiol: 2015; 53 1 237 247
    • (2015) J Clin Microbiol , vol.53 , Issue.1 , pp. 237-247
    • Stokell, J.R.1    Gharaibeh, R.Z.2    Hamp, T.J.3    Zapata, M.J.4    Fodor, A.A.5    Steck, T.R.6
  • 124
    • 84906658965 scopus 로고    scopus 로고
    • Antimicrobial resistance in the respiratory microbiota of people with cystic fibrosis
    • Sherrard L. J., Tunney M. M., Elborn J. S. Antimicrobial resistance in the respiratory microbiota of people with cystic fibrosis. Lancet: 2014; 384 9944 703 713
    • (2014) Lancet , vol.384 , Issue.9944 , pp. 703-713
    • Sherrard, L.J.1    Tunney, M.M.2    Elborn, J.S.3
  • 125
    • 84904000178 scopus 로고    scopus 로고
    • A preliminary quality of life questionnaire-bronchiectasis: A patient-reported outcome measure for bronchiectasis
    • Quittner A. L., Marciel K. K., Salathe M. A., et al. A preliminary quality of life questionnaire-bronchiectasis: a patient-reported outcome measure for bronchiectasis. Chest: 2014; 146 2 437 448
    • (2014) Chest , vol.146 , Issue.2 , pp. 437-448
    • Quittner, A.L.1    Marciel, K.K.2    Salathe, M.A.3
  • 126
    • 84919754878 scopus 로고    scopus 로고
    • Quality of Life Questionnaire-Bronchiectasis: Final psychometric analyses and determination of minimal important difference scores
    • Quittner A. L., O'Donnell A. E., Salathe M. A., et al. Quality of Life Questionnaire-Bronchiectasis: final psychometric analyses and determination of minimal important difference scores. Thorax: 2015; 70 1 12 20
    • (2015) Thorax , vol.70 , Issue.1 , pp. 12-20
    • Quittner, A.L.1    O'Donnell, A.E.2    Salathe, M.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.