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Volumn 61, Issue 5, 2015, Pages 707-715

Impact of sustained eradication of new pseudomonas aeruginosa infection on long-term outcomes in cystic fibrosis

Author keywords

Cystic fibrosis; Eradication therapy; Pseudomonas aeruginosa; Pseudomonas infections; Treatment outcomes

Indexed keywords

CIPROFLOXACIN; TOBRAMYCIN; ANTIINFECTIVE AGENT;

EID: 84942033101     PISSN: 10584838     EISSN: 15376591     Source Type: Journal    
DOI: 10.1093/cid/civ377     Document Type: Article
Times cited : (63)

References (31)
  • 1
    • 84869120178 scopus 로고    scopus 로고
    • Treatment of lung infection in patients with cystic fibrosis: Current and future strategies
    • Doring G, Flume P, Heijerman H, Elborn JS. Treatment of lung infection in patients with cystic fibrosis: current and future strategies. J Cyst Fibros 2012; 11:461-79.
    • (2012) J Cyst Fibros , vol.11 , pp. 461-479
    • Doring, G.1    Flume, P.2    Heijerman, H.3    Elborn, J.S.4
  • 2
    • 0036320272 scopus 로고    scopus 로고
    • Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis
    • Emerson J, Rosenfeld M, McNamara S, Ramsey B, Gibson RL. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatr Pulmonol 2002; 34:91-100.
    • (2002) Pediatr Pulmonol , vol.34 , pp. 91-100
    • Emerson, J.1    Rosenfeld, M.2    McNamara, S.3    Ramsey, B.4    Gibson, R.L.5
  • 3
    • 77950126962 scopus 로고    scopus 로고
    • Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis
    • Hewer SC, Smyth AR. Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis. Cochrane Database Syst Rev 2009; 4:CD004197.
    • (2009) Cochrane Database Syst Rev , vol.4 , pp. CD004197
    • Hewer, S.C.1    Smyth, A.R.2
  • 4
    • 84920412587 scopus 로고    scopus 로고
    • Cystic fibrosis pulmonary guideline: Pharmacologic approaches to prevention and eradication of initial Pseudomonas aeruginosa infection
    • Mogayzel PJ Jr, Naureckas ET, Roginson KA, et al. Cystic fibrosis pulmonary guideline: pharmacologic approaches to prevention and eradication of initial Pseudomonas aeruginosa infection. Ann Am Thorac Soc 2014; 11:1640-50.
    • (2014) Ann Am Thorac Soc , vol.11 , pp. 1640-1650
    • Mogayzel, P.J.1    Naureckas, E.T.2    Roginson, K.A.3
  • 5
    • 79955925867 scopus 로고    scopus 로고
    • The effect of early Pseudomonas aeruginosa treatment on lung function in pediatric cystic fibrosis
    • Amin R, Lam M, Dupuis A, Ratjen F. The effect of early Pseudomonas aeruginosa treatment on lung function in pediatric cystic fibrosis. Pediatr Pulmonol 2011; 46:554-8.
    • (2011) Pediatr Pulmonol , vol.46 , pp. 554-558
    • Amin, R.1    Lam, M.2    Dupuis, A.3    Ratjen, F.4
  • 6
    • 0027195501 scopus 로고
    • Prognostic implications of initial oropharyngeal bacterial flora in patients with cystic fibrosis diagnosed before the age of two years
    • Hudson VL, Wielinski CL, Regelmann WE. Prognostic implications of initial oropharyngeal bacterial flora in patients with cystic fibrosis diagnosed before the age of two years. J Pediatr 1993; 122:854-60.
    • (1993) J Pediatr , vol.122 , pp. 854-860
    • Hudson, V.L.1    Wielinski, C.L.2    Regelmann, W.E.3
  • 7
    • 0034785481 scopus 로고    scopus 로고
    • Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition
    • Kosorok MR, Zeng L,West SE, et al. Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition. Pediatr Pulmonol 2001; 32:277-87.
    • (2001) Pediatr Pulmonol , vol.32 , pp. 277-287
    • Kosorok, M.R.1    Zeng, L.2    West, S.E.3
  • 8
    • 46349106358 scopus 로고    scopus 로고
    • Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis
    • Kozlowska WJ, Bush A, Wade A, et al. Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis. Am J Respir Crit Care Med 2008; 178:42-9.
    • (2008) Am J Respir Crit Care Med , vol.178 , pp. 42-49
    • Kozlowska, W.J.1    Bush, A.2    Wade, A.3
  • 9
    • 84922681046 scopus 로고    scopus 로고
    • Clinical outcomes after initial Pseudomonas acquisition in cystic fibrosis
    • Zemanick ET, Emerson J, Thompson V, et al. Clinical outcomes after initial Pseudomonas acquisition in cystic fibrosis. Pediatr Pulmonol 2015; 50:42-8.
    • (2015) Pediatr Pulmonol , vol.50 , pp. 42-48
    • Zemanick, E.T.1    Emerson, J.2    Thompson, V.3
  • 10
    • 80052511405 scopus 로고    scopus 로고
    • Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis
    • Treggiari MM, Retsch-Bogart G, Mayer-Hamblett N, et al. Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis. Arch Pediatr Adolesc Med 2011; 165:847-56.
    • (2011) Arch Pediatr Adolesc Med , vol.165 , pp. 847-856
    • Treggiari, M.M.1    Retsch-Bogart, G.2    Mayer-Hamblett, N.3
  • 11
    • 77950914953 scopus 로고    scopus 로고
    • Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: The ELITE trial
    • Ratjen F, Munck A, Kho P, Angyalosi G. Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial. Thorax 2010; 65:286-91.
    • (2010) Thorax , vol.65 , pp. 286-291
    • Ratjen, F.1    Munck, A.2    Kho, P.3    Angyalosi, G.4
  • 12
    • 67349204479 scopus 로고    scopus 로고
    • Early anti-pseudomonal acquisition in young patients with cystic fibrosis: Rationale and design of the EPIC clinical trial and observational study
    • Treggiari MM, Rosenfeld M, Mayer-Hamblett N, et al. Early anti-pseudomonal acquisition in young patients with cystic fibrosis: rationale and design of the EPIC clinical trial and observational study. Contemp Clin Trials 2009; 30:256-68.
    • (2009) Contemp Clin Trials , vol.30 , pp. 256-268
    • Treggiari, M.M.1    Rosenfeld, M.2    Mayer-Hamblett, N.3
  • 13
    • 1642515022 scopus 로고    scopus 로고
    • Reduction in prevalence of chronic Pseudomonas aeruginosa infection at a regional pediatric cystic fibrosis center
    • Lee TW, Brownlee KG, Denton M, Littlewood JM, Conway SP. Reduction in prevalence of chronic Pseudomonas aeruginosa infection at a regional pediatric cystic fibrosis center. Pediatr Pulmonol 2004; 37:104-10.
    • (2004) Pediatr Pulmonol , vol.37 , pp. 104-110
    • Lee, T.W.1    Brownlee, K.G.2    Denton, M.3    Littlewood, J.M.4    Conway, S.P.5
  • 14
    • 84907296644 scopus 로고    scopus 로고
    • Pseudomonas aeruginosa in vitro phenotypes distinguish cystic fibrosis infection stages and outcomes
    • Mayer-Hamblett N, Rosenfeld M, Gibson RL, et al. Pseudomonas aeruginosa in vitro phenotypes distinguish cystic fibrosis infection stages and outcomes. Am J Respir Crit Care Med 2014; 190:289-97.
    • (2014) Am J Respir Crit Care Med , vol.190 , pp. 289-297
    • Mayer-Hamblett, N.1    Rosenfeld, M.2    Gibson, R.L.3
  • 16
    • 0032926069 scopus 로고    scopus 로고
    • Spirometric reference values from a sample of the general U.S. Population
    • Hankinson JL, Odencrantz JR, Fedan KB. Spirometric reference values from a sample of the general U.S. population. Am J Respir Crit Care Med 1999; 159:179-87.
    • (1999) Am J Respir Crit Care Med , vol.159 , pp. 179-187
    • Hankinson, J.L.1    Odencrantz, J.R.2    Fedan, K.B.3
  • 17
    • 0030995361 scopus 로고    scopus 로고
    • Antibiotic treatment of initial colonization with Pseudomonas aeruginosa postpones chronic infection and prevents deterioration of pulmonary function in cystic fibrosis
    • Frederiksen B, Koch C, Hoiby N. Antibiotic treatment of initial colonization with Pseudomonas aeruginosa postpones chronic infection and prevents deterioration of pulmonary function in cystic fibrosis. Pediatr Pulmonol 1997; 23:330-5.
    • (1997) Pediatr Pulmonol , vol.23 , pp. 330-335
    • Frederiksen, B.1    Koch, C.2    Hoiby, N.3
  • 18
    • 55549102981 scopus 로고    scopus 로고
    • Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experience
    • Hansen CR, Pressler T, Hoiby N. Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experience. J Cyst Fibros 2008; 7:523-30.
    • (2008) J Cyst Fibros , vol.7 , pp. 523-530
    • Hansen, C.R.1    Pressler, T.2    Hoiby, N.3
  • 19
    • 0025868478 scopus 로고
    • Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment
    • Valerius NH, Koch C, Hoiby N. Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment. Lancet 1991; 338:725-6.
    • (1991) Lancet , vol.338 , pp. 725-726
    • Valerius, N.H.1    Koch, C.2    Hoiby, N.3
  • 22
    • 77951887288 scopus 로고    scopus 로고
    • Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: A randomized controlled trial
    • Saiman L, Anstead M, Mayer-Hamblett N, et al. Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: a randomized controlled trial. JAMA 2010; 303:1707-15.
    • (2010) JAMA , vol.303 , pp. 1707-1715
    • Saiman, L.1    Anstead, M.2    Mayer-Hamblett, N.3
  • 23
    • 0141816759 scopus 로고    scopus 로고
    • Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: A randomized controlled trial
    • Saiman L, Marshall BC, Mayer-Hamblett N, et al. Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial. JAMA 2003; 290:1749-56.
    • (2003) JAMA , vol.290 , pp. 1749-1756
    • Saiman, L.1    Marshall, B.C.2    Mayer-Hamblett, N.3
  • 24
    • 30944466084 scopus 로고    scopus 로고
    • A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
    • Elkins MR, Robinson M, Rose BR, et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 2006; 354:229-40.
    • (2006) N Engl J Med , vol.354 , pp. 229-240
    • Elkins, M.R.1    Robinson, M.2    Rose, B.R.3
  • 25
    • 38349058630 scopus 로고    scopus 로고
    • A phase 2 study of aztreonam lysine for inhalation to treat patients with cystic fibrosis and Pseudomonas aeruginosa infection
    • Retsch-Bogart GZ, Burns JL, Otto KL, et al. A phase 2 study of aztreonam lysine for inhalation to treat patients with cystic fibrosis and Pseudomonas aeruginosa infection. Pediatr Pulmonol 2008; 43: 47-58.
    • (2008) Pediatr Pulmonol , vol.43 , pp. 47-58
    • Retsch-Bogart, G.Z.1    Burns, J.L.2    Otto, K.L.3
  • 26
    • 12844270608 scopus 로고    scopus 로고
    • Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis
    • Li Z, Kosorok MR, Farrell PM, et al. Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis. JAMA 2005; 293:581-8.
    • (2005) JAMA , vol.293 , pp. 581-588
    • Li, Z.1    Kosorok, M.R.2    Farrell, P.M.3
  • 27
    • 84942029666 scopus 로고    scopus 로고
    • Trends in respiratory microbiology of people with cystic fibrosis in the United States, 2006-2012 (Abstract)
    • Knapp EA, Salsgiver E, Fink A, Sewall A, Marshall BC, Saiman L. Trends in respiratory microbiology of people with cystic fibrosis in the United States, 2006-2012 (Abstract). Pediatr Pulmonol 2014; (suppl 38):317.
    • (2014) Pediatr Pulmonol , pp. 317
    • Knapp, E.A.1    Salsgiver, E.2    Fink, A.3    Sewall, A.4    Marshall, B.C.5    Saiman, L.6
  • 28
    • 84355161775 scopus 로고    scopus 로고
    • Evolution and diversification of Pseudomonas aeruginosa in the paranasal sinuses of cystic fibrosis children have implications for chronic lung infection
    • Hansen SK, Rau MH, Johansen HK, et al. Evolution and diversification of Pseudomonas aeruginosa in the paranasal sinuses of cystic fibrosis children have implications for chronic lung infection. ISME J 2012; 6:31-45.
    • (2012) ISME J , vol.6 , pp. 31-45
    • Hansen, S.K.1    Rau, M.H.2    Johansen, H.K.3
  • 29
    • 0032718969 scopus 로고    scopus 로고
    • Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis
    • Rosenfeld M, Emerson J, Accurso F, et al. Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis. Pediatr Pulmonol 1999; 28:321-8.
    • (1999) Pediatr Pulmonol , vol.28 , pp. 321-328
    • Rosenfeld, M.1    Emerson, J.2    Accurso, F.3
  • 30
    • 84878014012 scopus 로고    scopus 로고
    • Pseudomonas aeruginosa serology and risk for re-isolation in the EPIC trial
    • Anstead M, Heltshe SL, Khan U, et al. Pseudomonas aeruginosa serology and risk for re-isolation in the EPIC trial. J Cyst Fibros 2013; 12:147-53.
    • (2013) J Cyst Fibros , vol.12 , pp. 147-153
    • Anstead, M.1    Heltshe, S.L.2    Khan, U.3
  • 31
    • 84926130841 scopus 로고    scopus 로고
    • Serology as a diagnostic tool for predicting initial Pseudomonas aeruginosa acquisition in children with cystic fibrosis
    • Daines C, VanDeVanter D, Khan U, et al. Serology as a diagnostic tool for predicting initial Pseudomonas aeruginosa acquisition in children with cystic fibrosis. J Cyst Fibros 2014; 13:542-9.
    • (2014) J Cyst Fibros , vol.13 , pp. 542-549
    • Daines, C.1    VanDeVanter, D.2    Khan, U.3


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