dc.creator | Da Silva Filho L.V.R.F. | |
dc.creator | Ferreira F.A. | |
dc.creator | Reis F.J.C. | |
dc.creator | De Britto M.C.A. | |
dc.creator | Levy C.E. | |
dc.creator | Clark O. | |
dc.creator | Ribeiro J.D. | |
dc.date | 2013 | |
dc.date | 2015-06-25T19:09:57Z | |
dc.date | 2015-11-26T14:56:56Z | |
dc.date | 2015-06-25T19:09:57Z | |
dc.date | 2015-11-26T14:56:56Z | |
dc.date.accessioned | 2018-03-28T22:08:52Z | |
dc.date.available | 2018-03-28T22:08:52Z | |
dc.identifier | | |
dc.identifier | Jornal Brasileiro De Pneumologia. , v. 39, n. 4, p. 495 - 512, 2013. | |
dc.identifier | 18063713 | |
dc.identifier | | |
dc.identifier | http://www.scopus.com/inward/record.url?eid=2-s2.0-84884733385&partnerID=40&md5=e3899ff4cbe12cc1303a267155ec38df | |
dc.identifier | http://www.repositorio.unicamp.br/handle/REPOSIP/88406 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/88406 | |
dc.identifier | 2-s2.0-84884733385 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1255557 | |
dc.description | Evidence-based techniques have been increasingly used in the creation of clinical guidelines and the development of recommendations for medical practice. The use of levels of evidence allows the reader to identify the quality of scientific information that supports the recommendations made by experts. The objective of this review was to address current concepts related to the clinical impact, diagnosis, and treatment of Pseudomonas aeruginosa infections in patients with cystic fibrosis. For the preparation of this review, the authors defined a group of questions that would be answered in accordance with the principles of PICO-an acronym based on questions regarding the Patients of interest, Intervention being studied, Comparison of the intervention, and Outcome of interest. For each question, a structured review of the literature was performed using the Medline database in order to identify the studies with the methodological design most appropriate to answering the question. The questions were designed so that each of the authors could write a response. A first draft was prepared and discussed by the group. Recommendations were then made on the basis of the level of scientific evidence, in accordance with the classification system devised by the Oxford Centre for Evidence-Based Medicine, as well as the level of agreement among the members of the group. | |
dc.description | 39 | |
dc.description | 4 | |
dc.description | 495 | |
dc.description | 512 | |
dc.description | Ratjen, F., Döring, G., Cystic fibrosis (2003) Lancet, 361 (9358), pp. 681-689. , http://dx.doi.org/10.1016/S0140-6736(03)12567-6 | |
dc.description | Flume, P.A., O'Sullivan, B.P., Robinson, K.A., Goss, C.H., Mogayzel Jr., P.J., Willey-Courand, D.B., Cystic fibrosis pulmonary guidelines: Chronic medications for maintenance of lung health (2007) Am J Respir Crit Care Med, 176 (10), pp. 957-969. , http://dx.doi.org/10.1164/rccm.200705-664OC, PMid:17761616 | |
dc.description | Ratjen, F.A., Cystic fibrosis: Pathogenesis and future treatment strategies (2009) Respir Care, 54 (5), pp. 595-605. , http://dx.doi.org/10.4187/aarc0427, PMid:19393104 | |
dc.description | Lommatzsch, S.T., Aris, R., Genetics of cystic fibrosis (2009) Semin Respir Crit Care Med, 30 (5), pp. 531-538. , http://dx.doi.org/10.1055/s-0029-1238911, PMid:19760540 | |
dc.description | Ratjen, F., Diagnosing and managing infection in CF Paediatr Respir Rev. 2006;7 Suppl, 1, pp. 151-153. , http://dx.doi.org/10.1016/j.prrv.2006.04.217, PMid:16798546 | |
dc.description | Govan, J.R., Deretic, V., Microbial pathogenesis in cystic fibrosis: Mucoid Pseudomonas aeruginosa and Burkholderia cepacia (1996) Microbiol Rev, 60 (3), pp. 539-574. , PMid:8840786 PMCid:239456 | |
dc.description | Li, Z., Kosorok, M.R., Farrell, P.M., Laxova, A., West, S.E., Green, C.G., Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis (2005) JAMA, 293 (5), pp. 581-588. , http://dx.doi.org/10.1001/jama.293.5.581, PMid:15687313 | |
dc.description | Gibson, R.L., Burns, J.L., Ramsey, B.W., Pathophysiology and management of pulmonary infections in cystic fibrosis (2003) Am J Respir Crit Care Med, 168 (8), pp. 918-951. , http://dx.doi.org/10.1164/rccm.200304-505SO, PMid:14555458 | |
dc.description | Deschaght, P., van Daele, S., de Baets, F., Vaneechoutte, M., PCR and the detection of Pseudomonas aeruginosa in respiratory samples of CF patients. A literature review (2011) J Cyst Fibros, 10 (5), pp. 293-297. , http://dx.doi.org/10.1016/j.jcf.2011.05.004, PMid:21684819 | |
dc.description | Nixon, G.M., Armstrong, D.S., Carzino, R., Carlin, J.B., Olinsky, A., Robertson, C.F., Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis (2001) J Pediatr, 138 (5), pp. 699-704. , http://dx.doi.org/10.1067/mpd.2001.112897, PMid:11343046 | |
dc.description | Henry, R.L., Mellis, C.M., Petrovic, L., Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis (1992) Pediatr Pulmonol, 12 (3), pp. 158-161. , http://dx.doi.org/10.1002/ppul.1950120306, PMid:1641272 | |
dc.description | Taccetti, G., Campana, S., Festini, F., Mascherini, M., Döring, G., Early eradication therapy against Pseudomonas aeruginosa in cystic fibrosis patients (2005) Eur Respir J, 26 (3), pp. 458-461. , http://dx.doi.org/10.1183/09031936.05.00009605, PMid:16135728 | |
dc.description | The Oxford 2011 Levels of Evidence, , http://www.cebm.net/index.aspx?o=5653, CEBM Centre For Evidence Based Medicine [homepage on the Internet]. Oxford: University of Oxford. [cited 2013 Feb 11] | |
dc.description | Lee, T.W., Brownlee, K.G., Conway, S.P., Denton, M., Littlewood, J.M., Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients (2003) J Cyst Fibros, 2 (1), pp. 29-34. , http://dx.doi.org/10.1016/S1569-1993(02)00141-8 | |
dc.description | Corey, M., Survival estimates in cystic fibrosis: Snapshots of a moving target (1996) Pediatr Pulmonol, 21 (3), pp. 149-150. , http://dx.doi.org/10.1002/1099-0496(199603)21:3149::AID-PPUL19502103023.0.CO;2-C | |
dc.description | Hudson, V.L., Wielinski, C.L., Regelmann, W.E., Prognostic implications of initial oropharyngeal bacterial flora in patients with cystic fibrosis diagnosed before the age of two years (1993) J Pediatr, 122 (6), pp. 854-860. , http://dx.doi.org/10.1016/S0022-3476(09)90007-5 | |
dc.description | Kosorok, M.R., Zeng, L., West, S.E., Rock, M.J., Splaingard, M.L., Laxova, A., Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition (2001) Pediatr Pulmonol, 32 (4), pp. 277-287. , http://dx.doi.org/10.1002/ppul.2009.abs, PMid:11568988 | |
dc.description | Emerson, J., Rosenfeld, M., McNamara, S., Ramsey, B., Gibson, R.L., Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis (2002) Pediatr Pulmonol, 34 (2), pp. 91-100. , http://dx.doi.org/10.1002/ppul.10127, PMid:12112774 | |
dc.description | Lebecque, P., Leal, T., Zylberberg, K., Reychler, G., Bossuyt, X., Godding, V., Towards zero prevalence of chronic Pseudomonas aeruginosa infection in children with cystic fibrosis (2006) J Cyst Fibros, 5 (4), pp. 237-244. , http://dx.doi.org/10.1016/j.jcf.2006.04.001, PMid:16790367 | |
dc.description | Ratjen, F., Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis (2006) Curr Opin Pulm Med, 12 (6), pp. 428-432. , http://dx.doi.org/10.1097/01.mcp.0000245712.51514.a1, PMid:17053493 | |
dc.description | Equi, A.C., Pike, S.E., Davies, J., Bush, A., Use of cough swabs in a cystic fibrosis clinic (2001) Arch Dis Child, 85 (5), pp. 438-439. , http://dx.doi.org/10.1136/adc.85.5.438, PMid:11668115 PMCid:1718986 | |
dc.description | Da Silva Filho, L.V., Tateno, A.F., Martins, K.M., Azzuz Chernishev, A.C., de Garcia, D.O., Haug, M., The combination of PCR and serology increases the diagnosis of Pseudomonas aeruginosa colonization/infection in cystic fibrosis (2007) Pediatr Pulmonol, 42 (10), pp. 938-944. , http://dx.doi.org/10.1002/ppul.20686, PMid:17722007 | |
dc.description | Hoiby, N., Flensborg, E.W., Beck, B., Friis, B., Jacobsen, S.V., Jacobsen, L., Pseudomonas aeruginosa infection in cystic fibrosis. Diagnostic and prognostic significance of Pseudomonas aeruginosa precipitins determined by means of crossed immunoelectrophoresis (1977) Scand J Respir Dis, 58 (2), pp. 65-79. , PMid:404701 | |
dc.description | Brett, M.M., Ghoneim, A.T., Littlewood, J.M., Prediction and diagnosis of early Pseudomonas aeruginosa infection in cystic fibrosis: A follow-up study (1988) J Clin Microbiol, 26 (8), pp. 1565-1570. , Erratum in: J Clin Microbiol 1989;27(1):230. PMid:3139707 PMCid:266661 | |
dc.description | West, S.E., Zeng, L., Lee, B.L., Kosorok, M.R., Laxova, A., Rock, M.J., Respiratory infections with Pseudomonas aeruginosa in children with cystic fibrosis: Early detection by serology and assessment of risk factors (2002) JAMA, 287 (22), pp. 2958-2967. , http://dx.doi.org/10.1001/jama.287.22.2958, PMid:12052125 | |
dc.description | Kappler, M., Kraxner, A., Reinhardt, D., Ganster, B., Griese, M., Lang, T., Diagnostic and prognostic value of serum antibodies against Pseudomonas aeruginosa in cystic fibrosis (2006) Thorax, 61 (8), pp. 684-688. , http://dx.doi.org/10.1136/thx.2005.049536, PMid:16449259 PMCid:2104684 | |
dc.description | Tramper-Stranders, G.A., van der Ent, C.K., Slieker, M.G., Terheggen-Lagro, S.W., Teding van Berkhout, F., Kimpen, J.L., Diagnostic value of serological tests against Pseudomonas aeruginosa in a large cystic fibrosis population (2006) Thorax, 61 (8), pp. 689-693. , http://dx.doi.org/10.1136/thx.2005.054726, PMid:16601093 PMCid:2104678 | |
dc.description | Ratjen, F., Walter, H., Haug, M., Meisner, C., Grasemann, H., Döring, G., Diagnostic value of serum antibodies in early Pseudomonas aeruginosa infection in cystic fibrosis patients (2007) Pediatr Pulmonol, 42 (3), pp. 249-255. , http://dx.doi.org/10.1002/ppul.20562, PMid:17243185 | |
dc.description | Weisner, A.M., Chart, H., Bush, A., Davies, J.C., Pitt, T.L., Detection of antibodies to Pseudomonas aeruginosa in serum and oral fluid from patients with cystic fibrosis (2007) J Med Microbiol, 56 (PART 5), pp. 670-674. , http://dx.doi.org/10.1099/jmm.0.46833-0, PMid:17446292 | |
dc.description | Pressler, T., Karpati, F., Granström, M., Knudsen, P.K., Lindblad, A., Hjelte, L., Diagnostic significance of measurements of specific IgG antibodies to Pseudomonas aeruginosa by three different serological methods (2009) J Cyst Fibros, 8 (1), pp. 37-42. , http://dx.doi.org/10.1016/j.jcf.2008.08.002, PMid:18835753 | |
dc.description | Milagres, L.G., Castro, T.L., Garcia, D., Cruz, A.C., Higa, L., Folescu, T., Antibody response to Pseudomonas aeruginosa in children with cystic fibrosis (2009) Pediatr Pulmonol, 44 (4), pp. 392-401. , http://dx.doi.org/10.1002/ppul.21022, PMid:19283764 | |
dc.description | Hayes Jr., D., Farrell, P.M., Li, Z., West, S.E., Pseudomonas aeruginosa serological analysis in young children with cystic fibrosis diagnosed through newborn screening (2010) Pediatr Pulmonol, 45 (1), pp. 55-61. , http://dx.doi.org/10.1002/ppul.21083, PMid:20025049 PMCid:2924665 | |
dc.description | Douglas, T.A., Brennan, S., Berry, L., Winfield, K., Wainwright, C.E., Grimwood, K., Value of serology in predicting Pseudomonas aeruginosa infection in young children with cystic fibrosis (2010) Thorax, 65 (11), pp. 985-990. , http://dx.doi.org/10.1136/thx.2009.132845, PMid:20889526 | |
dc.description | Wainwright, C.E., Vidmar, S., Armstrong, D.S., Byrnes, C.A., Carlin, J.B., Cheney, J., Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: A randomized trial (2011) JAMA, 306 (2), pp. 163-171. , http://dx.doi.org/10.1001/jama.2011.954, PMid:21750293 | |
dc.description | Littlewood, J.M., Miller, M.G., Ghoneim, A.T., Ramsden, C.H., Nebulised colomycin for early pseudomonas colonisation in cystic fibrosis (1985) Lancet, 1 (8433), p. 865. , http://dx.doi.org/10.1016/S0140-6736(85)92222-6 | |
dc.description | Valerius, N.H., Koch, C., Høiby, N., Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment (1991) Lancet, 338 (8769), pp. 725-726. , http://dx.doi.org/10.1016/0140-6736(91)91446-2 | |
dc.description | Munck, A., Bonacorsi, S., Mariani-Kurkdjian, P., Lebourgeois, M., Gérardin, M., Brahimi, N., Genotypic characterization of Pseudomonas aeruginosa strains recovered from patients with cystic fibrosis after initial and subsequent colonization (2001) Pediatr Pulmonol, 32 (4), pp. 288-292. , http://dx.doi.org/10.1002/ppul.1121, PMid:11568989 | |
dc.description | Gibson, R.L., Emerson, J., McNamara, S., Burns, J.L., Rosenfeld, M., Yunker, A., Significant microbiological effect of inhaled tobramycin in young children with cystic fibrosis (2003) Am J Respir Crit Care Med, 167 (6), pp. 841-849. , http://dx.doi.org/10.1164/rccm.200208-855OC, PMid:12480612 | |
dc.description | Davidson, A.G., Chilvers, M.A., Lillquist, Y.P., Effects of a Pseudomonas aeruginosa eradication policy in a cystic fibrosis clinic (2012) Curr Opin Pulm Med, 18 (6), pp. 615-621. , http://dx.doi.org/10.1097/MCP.0b013e328358f5a2, PMid:22990661 | |
dc.description | Ratjen, F., Munck, A., Kho, P., Angyalosi, G., ELITE Study Group. Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: The ELITE trial (2010) Thorax, 65 (4), pp. 286-291. , http://dx.doi.org/10.1136/thx.2009.121657, PMid:19996339 | |
dc.description | Treggiari, M.M., Retsch-Bogart, G., Mayer-Hamblett, N., Khan, U., Kulich, M., Kronmal, R., Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis (2011) Arch Pediatr Adolesc Med, 165 (9), pp. 847-856. , http://dx.doi.org/10.1001/archpediatrics.2011.136, PMid:21893650 | |
dc.description | Langton Hewer, S.C., Smyth, A.R., Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis (2009) Cochrane Database Syst Rev, (4), pp. CD004197. , PMid:19821321 | |
dc.description | Collaco, J.M., Green, D.M., Cutting, G.R., Naughton, K.M., Mogayzel Jr., P.J., Location and duration of treatment of cystic fibrosis respiratory exacerbations do not affect outcomes (2010) Am J Respir Crit Care Med, 182 (9), pp. 1137-1143. , http://dx.doi.org/10.1164/rccm.201001-0057OC, PMid:20581166 PMCid:3001256 | |
dc.description | Fuchs, H.J., Borowitz, D.S., Christiansen, D.H., Morris, E.M., Nash, M.L., Ramsey, B.W., Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group (1994) N Engl J Med, 331 (10), pp. 637-642. , http://dx.doi.org/10.1056/NEJM199409083311003, PMid:7503821 | |
dc.description | Rosenfeld, M., Emerson, J., Williams-Warren, J., Pepe, M., Smith, A., Montgomery, A.B., Defining a pulmonary exacerbation in cystic fibrosis (2001) J Pediatr, 139 (3), pp. 359-365. , http://dx.doi.org/10.1067/mpd.2001.117288, PMid:11562614 | |
dc.description | Dakin, C., Henry, R.L., Field, P., Morton, J., Defining an exacerbation of pulmonary disease in cystic fibrosis (2001) Pediatr Pulmonol, 31 (6), pp. 436-442. , http://dx.doi.org/10.1002/ppul.1072, PMid:11389576 | |
dc.description | Flume, P.A., Mogayzel Jr., P.J., Robinson, K.A., Goss, C.H., Rosenblatt, R.L., Kuhn, R.J., Cystic fibrosis pulmonary guidelines: Treatment of pulmonary exacerbations (2009) Am J Respir Crit Care Med, 180 (9), pp. 802-808. , http://dx.doi.org/10.1164/rccm.200812-1845PP, PMid:19729669 | |
dc.description | Stenbit, A.E., Flume, P.A., Pulmonary exacerbations in cystic fibrosis (2011) Curr Opin Pulm Med, 17 (6), pp. 442-447. , PMid:21881509 | |
dc.description | Bilton, D., Canny, G., Conway, S., Dumcius, S., Hjelte, L., Proesmans, M., Pulmonary exacerbation: Towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials (2011) J Cyst Fibros, 10 (SUPPL. 2), pp. 79-81. , http://dx.doi.org/10.1016/S1569-1993(11)60012-X | |
dc.description | Balaguer, A., De Dios, G.J., Home versus hospital intravenous antibiotic therapy for cystic fibrosis (2012) Cochrane Database Syst Rev, 3, pp. CD001917. , PMid:22419283 | |
dc.description | Smyth, A., Elborn, J.S., Exacerbations in cystic fibrosis: 3. Management (2008) Thorax, 63 (2), pp. 180-184. , http://dx.doi.org/10.1136/thx.2006.060905, PMid:18234661 | |
dc.description | Smyth, A., Knox, A., Twice vs three times daily antibiotics in the treatment of pulmonary exacerbations of cystic fibrosis (2011) J Cyst Fibros, 10 (5), p. 383. , http://dx.doi.org/10.1016/j.jcf.2011.03.010, PMid:21507733 | |
dc.description | Breidenstein, E.B., de la Fuente-Nú-ez, C., Hancock, R.E., Pseudomonas aeruginosa: All roads lead to resistance (2011) Trends Microbiol, 19 (8), pp. 419-426. , http://dx.doi.org/10.1016/j.tim.2011.04.005, PMid:21664819 | |
dc.description | Cheng, K., Smyth, R.L., Govan, J.R., Doherty, C., Winstanley, C., Denning, N., Spread of beta-lactam-resistant Pseudomonas aeruginosa in a cystic fibrosis clinic (1996) Lancet, 348 (9028), pp. 639-642. , http://dx.doi.org/10.1016/S0140-6736(96)05169-0 | |
dc.description | Elphick, H.E., Tan, A., Single versus combination intravenous antibiotic therapy for people with cystic fibrosis (2005) Cochrane Database Syst Rev, (2), pp. CD002007. , PMid:15846627 | |
dc.description | Bosso, J.A., Saxon, B.A., Matsen, J.M., Comparative activity of cefepime, alone and in combination, against clinical isolates of Pseudomonas aeruginosa and Pseudomonas cepacia from cystic fibrosis patients (1991) Antimicrob Agents Chemother, 35 (4), pp. 783-784. , http://dx.doi.org/10.1128/AAC.35.4.783, PMid:1906264 PMCid:245101 | |
dc.description | Tré-Hardy, M., Nagant, C., El-Manssouri, N., Vanderbist, F., Traore, H., Vaneechoutte, M., Efficacy of the combination of tobramycin and a macrolide in an in vitro Pseudomonas aeruginosa mature biofilm model (2010) Antimicrob Agents Chemother, 54 (10), pp. 4409-4415. , http://dx.doi.org/10.1128/AAC.00372-10, PMid:20696878 PMCid:2944582 | |
dc.description | Leroy, A., Humbert, G., Oksenhendler, G., Fillastre, J.P., Pharmacokinetics of aminoglycosides in subjects with normal and impaired renal function (1978) Antibiot Chemother, 25, pp. 163-180. , PMid:352252 | |
dc.description | Kovarik, J.M., Hoepelman, I.M., Verhoef, J., Once-daily aminoglycoside administration: New strategies for an old drug (1989) Eur J Clin Microbiol Infect Dis, 8 (9), pp. 761-769. , http://dx.doi.org/10.1007/BF02185842, PMid:2512146 | |
dc.description | Freeman, C.D., Nicolau, D.P., Belliveau, P.P., Nightingale, C.H., Once-daily dosing of aminoglycosides: Review and recommendations for clinical practice (1997) J Antimicrob Chemother, 39 (6), pp. 677-686. , http://dx.doi.org/10.1093/jac/39.6.677, PMid:9222035 | |
dc.description | Contopoulos-Ioannidis, D.G., Giotis, N.D., Baliatsa, D.V., Ioannidis, J.P., Extended-interval aminoglycoside administration for children: A meta-analysis (2004) Pediatrics, 114 (1), pp. 111-118. , http://dx.doi.org/10.1542/peds.114.1.e111, PMid:15231982 | |
dc.description | Smyth, A.R., Bhatt, J., Once-daily versus multiple-daily dosing with intravenous aminoglycosides for cystic fibrosis (2012) Cochrane Database Syst Rev, 2, pp. CD002009. , PMid:22336782 | |
dc.description | Plummer, A., Wildman, M., Duration of intravenous antibiotic therapy in people with cystic fibrosis (2011) Cochrane Database Syst Rev, 1, pp. CD006682. , PMid:21249681 | |
dc.description | Vandevanter, D.R., O'Riordan, M.A., Blumer, J.L., Konstan, M.W., Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations (2010) Respir Res, 11, p. 137. , http://dx.doi.org/10.1186/1465-9921-11-137, PMid:20925941 PMCid:2959026 | |
dc.description | Hodson, M.E., Penketh, A.R., Batten, J.C., Aerosol carbenicillin and gentamicin treatment of Pseudomonas aeruginosa infection in patients with cystic fibrosis (1981) Lancet, 2 (8256), pp. 1137-1139. , http://dx.doi.org/10.1016/S0140-6736(81)90588-2 | |
dc.description | Szaff, M., Høiby, N., Flensborg, E.W., Frequent antibiotic therapy improves survival of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection (1983) Acta Paediatr Scand, 72 (5), pp. 651-657. , http://dx.doi.org/10.1111/j.1651-2227.1983.tb09789.x, PMid:6637463 | |
dc.description | Ramsey, B.W., Dorkin, H.L., Eisenberg, J.D., Gibson, R.L., Harwood, I.R., Kravitz, R.M., Efficacy of aerosolized tobramycin in patients with cystic fibrosis (1993) N Engl J Med, 328 (24), pp. 1740-1746. , http://dx.doi.org/10.1056/NEJM199306173282403, PMid:8497284 | |
dc.description | Ramsey, B.W., Pepe, M.S., Quan, J.M., Otto, K.L., Montgomery, A.B., Williams-Warren, J., Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group (1999) N Engl J Med, 340 (1), pp. 23-30. , http://dx.doi.org/10.1056/NEJM199901073400104, PMid:9878641 | |
dc.description | Maclusky, I.B., Gold, R., Corey, M., Levison, H., Long-term effects of inhaled tobramycin in patients with cystic fibrosis colonized with Pseudomonas aeruginosa (1989) Pediatr Pulmonol, 7 (1), pp. 42-48. , http://dx.doi.org/10.1002/ppul.1950070110, PMid:2505216 | |
dc.description | Murphy, T.D., Anbar, R.D., Lester, L.A., Nasr, S.Z., Nickerson, B., Vandevanter, D.R., Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung disease (2004) Pediatr Pulmonol, 38 (4), pp. 314-320. , http://dx.doi.org/10.1002/ppul.20097, PMid:15334509 | |
dc.description | (2009) Antibiotic Treatment For Cystic Fibrosis, , https://www.cysticfibrosis.org.uk/media/82010/CD_Antibiotic_treatment_for_CF_May_09.pdf, Cystic Fibrosis Trust [homepage on the Internet]. Bromley: Cystic Fibrosis Trust. [cited 2013 Feb 11], [Adobe Acrobat document, 102p.] | |
dc.description | Hodson, M.E., Gallagher, C.G., Govan, J.R., A randomised clinical trial of nebulised tobramycin or colistin in cystic fibrosis (2002) Eur Respir J, 20 (3), pp. 658-664. , http://dx.doi.org/10.1183/09031936.02.00248102, PMid:12358344 | |
dc.description | McCoy, K.S., Quittner, A.L., Oermann, C.M., Gibson, R.L., Retsch-Bogart, G.Z., Montgomery, A.B., Inhaled aztreonam lysine for chronic airway Pseudomonas aeruginosa in cystic fibrosis (2008) Am J Respir Crit Care Med, 178 (9), pp. 921-928. , http://dx.doi.org/10.1164/rccm.200712-1804OC, PMid:18658109 PMCid:2577727 | |
dc.description | Oermann, C.M., Retsch-Bogart, G.Z., Quittner, A.L., Gibson, R.L., McCoy, K.S., Montgomery, A.B., An 18-month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in cystic fibrosis (2010) Pediatr Pulmonol, 45 (11), pp. 1121-1134. , http://dx.doi.org/10.1002/ppul.21301, PMid:20672296 | |
dc.description | Konstan, M.W., Flume, P.A., Kappler, M., Chiron, R., Higgins, M., Brockhaus, F., Safety, efficacy and convenience of tobramycin inhalation powder in cystic fibrosis patients: The EAGER trial (2011) J Cyst Fibros, 10 (1), pp. 54-61. , http://dx.doi.org/10.1016/j.jcf.2010.10.003, PMid:21075062 | |
dc.description | Geller, D.E., Flume, P.A., Staab, D., Fischer, R., Loutit, J.S., Conrad, D.J., Levofloxacin inhalation solution (MP-376) in patients with cystic fibrosis with Pseudomonas aeruginosa (2011) Am J Respir Crit Care Med, 183 (11), pp. 1510-1516. , http://dx.doi.org/10.1164/rccm.201008-1293OC, PMid:21471106 | |
dc.description | Ryan, G., Singh, M., Dwan, K., Inhaled antibiotics for long-term therapy in cystic fibrosis (2011) Cochrane Database Syst Rev, (3), pp. CD001021 | |
dc.description | Sawicki, G.S., Tiddens, H., Managing treatment complexity in cystic fibrosis: Challenges and opportunities (2012) Pediatr Pulmonol, 47 (6), pp. 523-533. , http://dx.doi.org/10.1002/ppul.22546, PMid:22467341 | |
dc.description | Robinson, P., Cystic fibrosis (2001) Thorax, 56 (3), pp. 237-241. , http://dx.doi.org/10.1136/thorax.56.3.237, PMid:11182019 PMCid:1758774 | |
dc.description | Bell, S.C., Robinson, P.J., Exacerbations in cystic fibrosis: 2. prevention (2007) Thorax, 62 (8), pp. 723-732. , http://dx.doi.org/10.1136/thx.2006.060897, PMid:17687099 PMCid:2117269 | |
dc.description | Sawicki, G.S., Sellers, D.E., Robinson, W.M., High treatment burden in adults with cystic fibrosis: Challenges to disease self-management (2009) J Cyst Fibros, 8 (2), pp. 91-96. , http://dx.doi.org/10.1016/j.jcf.2008.09.007, PMid:18952504 PMCid:2680350 | |
dc.description | Milgrom, H., Bender, B., Ackerson, L., Bowry, P., Smith, B., Rand, C., Noncompliance and treatment failure in children with asthma (1996) J Allergy Clin Immunol, 98 (6 PART 1), pp. 1051-1057. , http://dx.doi.org/10.1016/S0091-6749(96)80190-4 | |
dc.description | Ievers, C.E., Brown, R.T., Drotar, D., Caplan, D., Pishevar, B.S., Lambert, R.G., Knowledge of physician prescriptions and adherence to treatment among children with cystic fibrosis and their mothers (1999) J Dev Behav Pediatr, 20 (5), pp. 335-343. , http://dx.doi.org/10.1097/00004703-199910000-00008, PMid:10533992 | |
dc.description | Rau, J.L., Determinants of patient adherence to an aerosol regimen (2005) Respir Care, 50 (10), pp. 1346-1356. , discussion 1357-9. PMid:16185370 | |
dc.description | Digirolamo, A.M., Quittner, A.L., Ackerman, V., Stevens, J., Identification and assessment of ongoing stressors in adolescents with a chronic illness: An application of the behavior-analytic model (1997) J Clin Child Psychol, 26 (1), pp. 53-66. , http://dx.doi.org/10.1207/s15374424jccp2601_6, PMid:9118176 | |
dc.description | Gudas, L.J., Koocher, G.P., Wypij, D., Perceptions of medical compliance in children and adolescents with cystic fibrosis (1991) J Dev Behav Pediatr, 12 (4), pp. 236-242. , http://dx.doi.org/10.1097/00004703-199108000-00004, PMid:1939678 | |
dc.description | Modi, A.C., Quittner, A.L., Barriers to treatment adherence for children with cystic fibrosis and asthma: What gets in the way? (2006) J Pediatr Psychol, 31 (8), pp. 846-858. , http://dx.doi.org/10.1093/jpepsy/jsj096, PMid:16401680 | |
dc.description | Dalcin Pde, T., Rampon, G., Pasin, L.R., Ramon, G.M., Abrahão, C.L., Oliveira, V.Z., Adherence to treatment in patients with cystic fibrosis (2007) J Bras Pneumol, 33 (6), pp. 663-670. , PMid:18200366 | |
dc.description | Eakin, M.N., Bilderback, A., Boyle, M.P., Mogayzel, P.J., Riekert, K.A., Longitudinal association between medication adherence and lung health in people with cystic fibrosis (2011) J Cyst Fibros, 10 (4), pp. 258-264. , http://dx.doi.org/10.1016/j.jcf.2011.03.005, PMid:21458391 PMCid:3114200 | |
dc.description | Briesacher, B.A., Quittner, A.L., Saiman, L., Sacco, P., Fouayzi, H., Quittell, L.M., Adherence with tobramycin inhaled solution and health care utilization (2011) BMC Pulm Med, 11, p. 5. , http://dx.doi.org/10.1186/1471-2466-11-5, PMid:21251275 PMCid:3033861 | |
dc.description | Shinkai, M., Rubin, B.K., Macrolides and airway inflammation in children (2005) Paediatr Respir Rev, 6 (3), pp. 227-235. , http://dx.doi.org/10.1016/j.prrv.2005.06.005, PMid:16153572 | |
dc.description | Kudoh, S., Uetake, T., Hagiwara, K., Hirayama, M., Hus, L.H., Kimura, H., Clinical effects of low-dose long-term erythromycin chemotherapy on diffuse panbronchiolitis (1987) Nihon Kyobu Shikkan Gakkai Zasshi, 25 (6), pp. 632-642. , Article in Japanese, PMid:3682440 | |
dc.description | McArdle, J.R., Talwalkar, J.S., Macrolides in cystic fibrosis (2007) Clin Chest Med, 28 (2), pp. 347-360. , http://dx.doi.org/10.1016/j.ccm.2007.02.005, PMid:17467553 | |
dc.description | Equi, A., Balfour-Lynn, I.M., Bush, A., Rosenthal, M., Long term azithromycin in children with cystic fibrosis: A randomised, placebo-controlled crossover trial (2002) Lancet, 360 (9338), pp. 978-984. , http://dx.doi.org/10.1016/S0140-6736(02)11081-6 | |
dc.description | Saiman, L., Marshall, B.C., Mayer-Hamblett, N., Burns, J.L., Quittner, A.L., Cibene, D.A., Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: A randomized controlled trial (2003) JAMA, 290 (13), pp. 1749-1756. , http://dx.doi.org/10.1001/jama.290.13.1749, PMid:14519709 | |
dc.description | Saiman, L., Anstead, M., Mayer-Hamblett, N., Lands, L.C., Kloster, M., Hocevar-Trnka, J., Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: A randomized controlled trial (2010) JAMA, 303 (17), pp. 1707-1715. , http://dx.doi.org/10.1001/jama.2010.563, PMid:20442386 | |
dc.description | Cai, Y., Chai, D., Wang, R., Bai, N., Liang, B.B., Liu, Y., Effectiveness and safety of macrolides in cystic fibrosis patients: A meta-analysis and systematic review (2011) J Antimicrob Chemother, 66 (5), pp. 968-978. , http://dx.doi.org/10.1093/jac/dkr040, PMid:21393178 | |
dc.description | Southern, K.W., Barker, P.M., Solis-Moya, A., Patel, L., Macrolide antibiotics for cystic fibrosis (2011) Cochrane Database Syst Rev, (12), pp. CD002203. , PMid:22161368 | |
dc.description | Smith, A.L., Fiel, S.B., Mayer-Hamblett, N., Ramsey, B., Burns, J.L., Susceptibility testing of Pseudomonas aeruginosa isolates and clinical response to parenteral antibiotic administration: Lack of association in cystic fibrosis (2003) Chest, 123 (5), pp. 1495-1502. , http://dx.doi.org/10.1378/chest.123.5.1495, PMid:12740266 | |
dc.description | Aaron, S.D., Vandemheen, K.L., Ferris, W., Fergusson, D., Tullis, E., Haase, D., Combination antibiotic susceptibility testing to treat exacerbations of cystic fibrosis associated with multiresistant bacteria: A randomised, double-blind, controlled clinical trial (2005) Lancet, 366 (9484), pp. 463-471. , http://dx.doi.org/10.1016/S0140-6736(05)67060-2 | |
dc.description | Cantón, R., Cobos, N., de Gracia, J., Baquero, F., Honorato, J., Gartner, S., Antimicrobial therapy for pulmonary pathogenic colonisation and infection by Pseudomonas aeruginosa in cystic fibrosis patients (2005) Clin Microbiol Infect, 11 (9), pp. 690-703. , http://dx.doi.org/10.1111/j.1469-0691.2005.01217.x, PMid:16104983 | |
dc.description | Saiman, L., Mehar, F., Niu, W.W., Neu, H.C., Shaw, K.J., Miller, G., Antibiotic susceptibility of multiply resistant Pseudomonas aeruginosa isolated from patients with cystic fibrosis, including candidates for transplantation (1996) Clin Infect Dis, 23 (3), pp. 532-537. , http://dx.doi.org/10.1093/clinids/23.3.532, PMid:8879776 | |
dc.description | Merlo, C.A., Boyle, M.P., Diener-West, M., Marshall, B.C., Goss, C.H., Lechtzin, N., Incidence and risk factors for multiple antibiotic-resistant Pseudomonas aeruginosa in cystic fibrosis (2007) Chest, 132 (2), pp. 562-568. , http://dx.doi.org/10.1378/chest.06-2888, PMid:17646236 | |
dc.description | Lechtzin, N., John, M., Irizarry, R., Merlo, C., Diette, G.B., Boyle, M.P., Outcomes of adults with cystic fibrosis infected with antibiotic-resistant Pseudomonas aeruginosa (2006) Respiration, 73 (1), pp. 27-33. , http://dx.doi.org/10.1159/000087686, PMid:16113513 | |
dc.language | en | |
dc.language | pt | |
dc.publisher | | |
dc.relation | Jornal Brasileiro de Pneumologia | |
dc.rights | aberto | |
dc.source | Scopus | |
dc.title | Pseudomonas Aeruginosa Infection In Patients With Cystic Fibrosis: Scientific Evidence Regarding Clinical Impact, Diagnosis, And Treatment [infecção Por Pseudomonas Aeruginosa Em Pacientes Com Fibrose Cística: Evidências Científicas Sobre O Impacto Clínico, Diagnóstico E Tratamento] | |
dc.type | Artículos de revistas | |