Outcomes and endpoints reported in studies of pulmonary exacerbations in people with cystic fibrosis: A systematic review.
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R. Norman | A. Smyth | C. Blyth | Sherie J Smith | A. Schultz | J. Wood | C. McLeod | S. Webb | T. Snelling | Jamie Wood
[1] A. Smyth,et al. Do current clinical trials in cystic fibrosis match the priorities of patients and clinicans? A systematic review. , 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[2] A. Gaggar,et al. Vitamin D for the Immune System in Cystic Fibrosis (DISC): a double-blind, multicenter, randomized, placebo-controlled clinical trial. , 2019, The American journal of clinical nutrition.
[3] G. Santyr,et al. Hyperpolarized Gas Magnetic Resonance Imaging of Pediatric Cystic Fibrosis Lung Disease. , 2019, Academic radiology.
[4] J. Emerson,et al. Initial development and pilot testing of observer-reported outcomes (ObsROs) for children with cystic fibrosis ages 0-11years. , 2018, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[5] A. Smyth,et al. P251 How does the current clinical trials landscape reflect the James Lind Alliance top ten research priorities for CF? , 2018, Journal of Cystic Fibrosis.
[6] Alicia J. French,et al. Procalcitonin, erythrocyte sedimentation rate and C‐reactive protein in acute pulmonary exacerbations of cystic fibrosis , 2018, The clinical respiratory journal.
[7] L. Saiman,et al. Meropenem time above the MIC exposure is predictive of response in cystic fibrosis children with acute pulmonary exacerbations. , 2018, Diagnostic microbiology and infectious disease.
[8] S. Stanojevic,et al. Lung clearance index to monitor treatment response in pulmonary exacerbations in preschool children with cystic fibrosis , 2018, Thorax.
[9] W. Morgan,et al. Treatment Setting and Outcomes of Cystic Fibrosis Pulmonary Exacerbations , 2017, Annals of the American Thoracic Society.
[10] D. Nicolau,et al. Use of ceftolozane-tazobactam in a cystic fibrosis patient with multidrug-resistant pseudomonas infection and renal insufficiency , 2017, Respiratory medicine case reports.
[11] D. Sanders,et al. Standardized Treatment of Pulmonary Exacerbations (STOP) study: Observations at the initiation of intravenous antibiotics for cystic fibrosis pulmonary exacerbations. , 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[12] D. Sanders,et al. Standardized Treatment of Pulmonary Exacerbations (STOP) study: Physician treatment practices and outcomes for individuals with cystic fibrosis with pulmonary Exacerbations. , 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[13] D. Sanders,et al. Rationalizing endpoints for prospective studies of pulmonary exacerbation treatment response in cystic fibrosis. , 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[14] E. Nash,et al. The top 10 research priorities in cystic fibrosis developed by a partnership between people with CF and healthcare providers , 2017, Thorax.
[15] Shuzhao Li,et al. Plasma metabolomics in adults with cystic fibrosis during a pulmonary exacerbation: A pilot randomized study of high-dose vitamin D3 administration. , 2017, Metabolism: clinical and experimental.
[16] C. Werner,et al. Chest physiotherapy can affect the lung clearance index in cystic fibrosis patients , 2017, Pediatric pulmonology.
[17] P. Hodgkins,et al. Frequency and costs of pulmonary exacerbations in patients with cystic fibrosis in the United States , 2017, Current medical research and opinion.
[18] H. Elphick,et al. Single versus combination intravenous anti-pseudomonal antibiotic therapy for people with cystic fibrosis. , 2016, The Cochrane database of systematic reviews.
[19] C. Schwarz,et al. Piperacillin-induced mild haemolytic anaemia in a 44-year-old patient with cystic fibrosis , 2016, BMJ Case Reports.
[20] Kurt A. Wargo,et al. Successful Use of Ceftolozane‐Tazobactam to Treat a Pulmonary Exacerbation of Cystic Fibrosis Caused by Multidrug‐Resistant Pseudomonas aeruginosa , 2016, Pharmacotherapy.
[21] M. Wildman,et al. Duration of intravenous antibiotic therapy in people with cystic fibrosis. , 2016, The Cochrane database of systematic reviews.
[22] Hans-Ulrich Kauczor,et al. Comparison of Lung Clearance Index and Magnetic Resonance Imaging for Assessment of Lung Disease in Children with Cystic Fibrosis , 2016, American journal of respiratory and critical care medicine.
[23] V. Waters,et al. Antibiotic treatment for Stenotrophomonas maltophilia in people with cystic fibrosis. , 2016, The Cochrane database of systematic reviews.
[24] T. Remmington,et al. Oral anti-pseudomonal antibiotics for cystic fibrosis. , 2016, The Cochrane database of systematic reviews.
[25] S. Stanojevic,et al. Physiologic endpoints for clinical studies for cystic fibrosis. , 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[26] M. Botteman,et al. Impact of pulmonary exacerbations and lung function on generic health-related quality of life in patients with cystic fibrosis , 2016, Health and Quality of Life Outcomes.
[27] A. Horsley,et al. Antibiotic treatment for Burkholderia cepacia complex in people with cystic fibrosis experiencing a pulmonary exacerbation. , 2016, The Cochrane database of systematic reviews.
[28] M. Elkins,et al. A randomised trial of hypertonic saline during hospitalisation for exacerbation of cystic fibrosis , 2016, Thorax.
[29] A. Balaguer,et al. Home versus hospital intravenous antibiotic therapy for cystic fibrosis. , 2015, The Cochrane database of systematic reviews.
[30] S. Stanojevic,et al. Factors associated with response to treatment of pulmonary exacerbations in cystic fibrosis patients. , 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[31] P. Flume,et al. Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis. , 2015, The Cochrane database of systematic reviews.
[32] S. Heltshe,et al. Effect of treatment of cystic fibrosis pulmonary exacerbations on systemic inflammation. , 2015, Annals of the American Thoracic Society.
[33] T. Willgoss,et al. Understanding the Suitability of Cystic Fibrosis-Specific Clinical Outcome Assessments For Clinical Trials and to Support Medical Product Labeling , 2015 .
[34] D. Sanders,et al. Short-term and long-term response to pulmonary exacerbation treatment in cystic fibrosis , 2015, Thorax.
[35] M. Wilschanski,et al. Cystic fibrosis and the role of gastrointestinal outcome measures in the new era of therapeutic CFTR modulation. , 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[36] H. Selvadurai,et al. A pilot study of inhaled dry-powder mannitol during cystic fibrosis-related pulmonary exacerbation , 2014, European Respiratory Journal.
[37] Al-AloulMohamed,et al. Nebulized tobramycin in the treatment of adult CF pulmonary exacerbations. , 2014 .
[38] M. Rybak,et al. Ceftaroline Fosamil for Methicillin-Resistant Staphylococcus aureus Pulmonary Exacerbation in a Pediatric Cystic Fibrosis Patient. , 2014, The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG.
[39] C. Terwee,et al. Core Outcome Measures in Effectiveness Trials (COMET) initiative: protocol for an international Delphi study to achieve consensus on how to select outcome measurement instruments for outcomes included in a ‘core outcome set’ , 2014, Trials.
[40] K. McCoy,et al. Osteopathic Manipulative Treatment for Inpatients With Pulmonary Exacerbations of Cystic Fibrosis: Effects on Spirometry Findings and Patient Assessments of Breathing, Anxiety, and Pain , 2014, The Journal of the American Osteopathic Association.
[41] H. Kauczor,et al. Magnetic resonance imaging detects changes in structure and perfusion, and response to therapy in early cystic fibrosis lung disease. , 2014, American journal of respiratory and critical care medicine.
[42] D. Sin,et al. Systematic review of blood biomarkers in cystic fibrosis pulmonary exacerbations. , 2013, Chest.
[43] K. Stiller,et al. Physical activity levels of patients with cystic fibrosis hospitalised with an acute respiratory exacerbation. , 2013, Respiratory medicine.
[44] S. Stick,et al. Novel end points for clinical trials in young children with cystic fibrosis , 2013, Expert review of respiratory medicine.
[45] T. Remmington,et al. Inhaled antibiotics for pulmonary exacerbations in cystic fibrosis. , 2013, Paediatric respiratory reviews.
[46] D. Hansell,et al. Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation , 2013, Thorax.
[47] H. Duivenvoorden,et al. Impact of bronchiectasis and trapped air on quality of life and exacerbations in cystic fibrosis , 2013, European Respiratory Journal.
[48] Marleen de Bruijne,et al. Chest computed tomography scores are predictive of survival in patients with cystic fibrosis awaiting lung transplantation. , 2012, American journal of respiratory and critical care medicine.
[49] B. Stanton,et al. Iron Homeostasis during Cystic Fibrosis Pulmonary Exacerbation , 2012, Clinical and translational science.
[50] R. Lyles,et al. Impact of vitamin D supplementation on markers of inflammation in adults with cystic fibrosis hospitalized for a pulmonary exacerbation , 2012, European Journal of Clinical Nutrition.
[51] F. Cameron,et al. Glucose Tolerance during Pulmonary Exacerbations in Children with Cystic Fibrosis , 2011, PloS one.
[52] J. Carlin,et al. Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: a randomized trial. , 2011, JAMA.
[53] R. Fischer,et al. Levofloxacin inhalation solution (MP-376) in patients with cystic fibrosis with Pseudomonas aeruginosa. , 2011, American journal of respiratory and critical care medicine.
[54] E. Baraldi,et al. Endpoints in respiratory diseases , 2011, European Journal of Clinical Pharmacology.
[55] M. O'riordan,et al. Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations , 2010, Respiratory research.
[56] D. Seder,et al. Piperacillin-Induced Immune Hemolytic Anemia in an Adult with Cystic Fibrosis , 2010, Case reports in medicine.
[57] M. Hodson,et al. Short-term comparative study of high frequency chest wall oscillation and European airway clearance techniques in patients with cystic fibrosis , 2009, Thorax.
[58] P. Watter,et al. Quality of life in young people with cystic fibrosis: effects of hospitalization, age and gender, and differences in parent/child perceptions. , 2009, Child: care, health and development.
[59] C. Cracowski,et al. Continuous versus Intermittent Infusions of Ceftazidime for Treating Exacerbation of Cystic Fibrosis , 2009, Antimicrobial Agents and Chemotherapy.
[60] A. Quittner,et al. Determination of the minimal clinically important difference scores for the Cystic Fibrosis Questionnaire-Revised respiratory symptom scale in two populations of patients with cystic fibrosis and chronic Pseudomonas aeruginosa airway infection. , 2009, Chest.
[61] D. Reinhardt,et al. Efficacy and safety of intravenous meropenem and tobramycin versus ceftazidime and tobramycin in cystic fibrosis. , 2008, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[62] C. Goss,et al. Patient-reported outcomes in cystic fibrosis. , 2007, Proceedings of the American Thoracic Society.
[63] M. Rosenfeld,et al. Endpoints for clinical trials in young children with cystic fibrosis. , 2007, Proceedings of the American Thoracic Society.
[64] B. Yankaskas,et al. Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis. , 2007, American journal of respiratory and critical care medicine.
[65] J. Elborn,et al. Clinical trials in cystic fibrosis. , 2007, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[66] B. Assael,et al. Chest physiotherapy with positive airway pressure: a pilot study of short-term effects on sputum clearance in patients with cystic fibrosis and severe airway obstruction. , 2006, Respiratory care.
[67] I. Abdulhamid,et al. Home versus hospital intravenous antibiotic therapy for acute pulmonary exacerbations in children with cystic fibrosis , 2006, Pediatric pulmonology.
[68] G. Hafen,et al. Clinical scoring systems in cystic fibrosis , 2006, Pediatric pulmonology.
[69] P. Ohtake,et al. Physiologic evidence for high-frequency chest wall oscillation and positive expiratory pressure breathing in hospitalized subjects with cystic fibrosis. , 2005, Physical therapy.
[70] L. Saiman,et al. The efficacy and safety of meropenem and tobramycin vs ceftazidime and tobramycin in the treatment of acute pulmonary exacerbations in patients with cystic fibrosis. , 2005, Chest.
[71] P. Bye,et al. Combination antibiotic susceptibility testing to treat exacerbations of cystic fibrosis associated with multiresistant bacteria: a randomised, double-blind, controlled clinical trial , 2005, The Lancet.
[72] P. Watter,et al. Respiratory exacerbations in children with cystic fibrosis: Physiotherapy treatment outcomes , 2005, Physiotherapy theory and practice.
[73] V. Lucidi,et al. Resting energy expenditure in young patients with cystic fibrosis receiving antibiotic therapy for acute respiratory exacerbations. , 2002, Clinical nutrition.
[74] P. Baghurst,et al. Efficacy of once‐daily tobramycin monotherapy for acute pulmonary exacerbations of cystic fibrosis: A preliminary study * , 2001, Pediatric pulmonology.
[75] Bowerman,et al. Metabolic and inflammatory responses to pulmonary exacerbation in adults with cystic fibrosis , 2000, European journal of clinical investigation.
[76] D. Orenstein,et al. Comparison of flutter device and chest physical therapy in the treatment of cystic fibrosis pulmonary exacerbation , 1999, Pediatric pulmonology.
[77] J. Kanga,et al. Cystic fibrosis clinical score: a new scoring system to evaluate acute pulmonary exacerbation. , 1999, Clinical therapeutics.
[78] G. Redding,et al. Comparison of a β-lactam alone versus β-lactam and an aminoglycoside for pulmonary exacerbation in cystic fibrosis , 1999 .
[79] F. Kelly,et al. Treatment of pulmonary exacerbations of cystic fibrosis leads to improved antioxidant status. , 1999, The European respiratory journal.
[80] D. Homnick,et al. Comparison of the flutter device to standard chest physiotherapy in hospitalized patients with cystic fibrosis: a pilot study. , 1998, Chest.
[81] D. Schidlow,et al. Pulmonary function in hospitalized infants and toddlers with cystic fibrosis. , 1998, The Journal of pediatrics.
[82] L. Breysem,et al. Treatment of Pseudomonas aeruginosa lung infection in cystic fibrosis with high or conventional doses of ceftazidime. , 1998, The Journal of antimicrobial chemotherapy.
[83] V. Stallings,et al. Acute pulmonary exacerbation is not associated with increased energy expenditure in children with cystic fibrosis. , 1998, The Journal of pediatrics.
[84] S. Conway,et al. Intravenous colistin sulphomethate in acute respiratory exacerbations in adult patients with cystic fibrosis. , 1997, Thorax.
[85] D. Nielson,et al. Effectiveness of home versus hospital care in the routine treatment of cystic fibrosis , 1997, Pediatric pulmonology.
[86] F. Gottrand,et al. Nutritional impact of antipseudomonas intravenous antibiotic courses in cystic fibrosis , 1997, Archives of disease in childhood.
[87] D. Turck,et al. Tolerance, pharmacokinetics and efficacy of once daily amikacin for treatment of Pseudomonas aeruginosa pulmonary exacerbations in cystic fibrosis patients , 1996, European Journal of Pediatrics.
[88] C. Delacourt,et al. Correlation between activity of beta-lactam agents in vitro and bacteriological outcome in acute pulmonary exacerbations of cystic fibrosis , 1995, European Journal of Clinical Microbiology and Infectious Diseases.
[89] L. Zanolla,et al. Short‐term effects of three chest physiotherapy regimens in patients hospitalized for pulmonary exacerbations of cystic fibrosis: A cross‐over randomized study , 1995, Pediatric pulmonology.
[90] M. Newport,et al. Home versus hospital intravenous antibiotic therapy in the treatment of young adults with cystic fibrosis. , 1994, The European respiratory journal.
[91] M. Hodson,et al. Comparison of nebulized and intravenous terbutaline during exacerbations of pulmonary infection in patients with cystic fibrosis. , 1992, The European respiratory journal.
[92] E. Valletta,et al. Modification of some markers of inflammation during treatment for acute respiratory exacerbation in cystic fibrosis , 1992, Acta paediatrica.
[93] J. A. Cooper,et al. Comparison of 6 and 8 hourly tobramycin dosing intervals in treatment of pulmonary exacerbations in cystic fibrosis patients. , 1991, The Pediatric infectious disease journal.
[94] M. Zach,et al. Chest physiotherapy in hospitalized patients with cystic fibrosis: a study of lung function effects and sputum production. , 1991, The European respiratory journal.
[95] W. Warwick,et al. Reduction of sputum Pseudomonas aeruginosa density by antibiotics improves lung function in cystic fibrosis more than do bronchodilators and chest physiotherapy alone. , 1990, The American review of respiratory disease.
[96] R. Kraemer,et al. Antipseudomonal therapy in cystic fibrosis: Aztreonam and amikacin versus ceftazidime and amikacin administered intravenously followed by oral ciprofloxacin , 1989, European Journal of Clinical Microbiology and Infectious Diseases.
[97] R. Cowan,et al. Intravenous immune globulin treatment of pulmonary exacerbations in cystic fibrosis. , 1989, The Journal of pediatrics.
[98] L. Ward,et al. Short-term nutritional supplementation during management of pulmonary exacerbations in cystic fibrosis: a controlled study, including effects of protein turnover. , 1988, The American journal of clinical nutrition.
[99] J. Bosso,et al. Controlled trial of aztreonam vs. tobramycin and azlocillin for acute pulmonary exacerbations of cystic fibrosis. , 1988, The Pediatric infectious disease journal.
[100] H. Auerbach,et al. Prospective controlled study of home and hospital therapy of cystic fibrosis pulmonary disease. , 1987, The Journal of pediatrics.
[101] A. Giunta,et al. Ceftazidime monotherapy vs. combined therapy in Pseudomonas pulmonary infections in cystic fibrosis. , 1987, The Pediatric infectious disease journal.
[102] J. Bosso,et al. Ciprofloxacin versus tobramycin plus azlocillin in pulmonary exacerbations in adult patients with cystic fibrosis. , 1987, The American journal of medicine.
[103] R. Stern,et al. Ciprofloxacin monotherapy for acute pulmonary exacerbations of cystic fibrosis. , 1987, The American journal of medicine.
[104] M. Jackson,et al. Comparison of piperacillin vs. ticarcillin plus tobramycin in the treatment of acute pulmonary exacerbations of cystic fibrosis. , 1986, Pediatric infectious disease.
[105] R. Kraemer,et al. Antimicrobial Therapy of Pseudomonas Pulmonary Exacerbations in Cystic Fibrosis , 1986, Acta paediatrica Scandinavica.
[106] A. Prince,et al. Treatment of lower respiratory tract infections due to Pseudomonas aeruginosa in patients with cystic fibrosis. , 1985, Reviews of infectious diseases.
[107] A. Olinsky,et al. The role of piperacillin therapy in pulmonary exacerbations of cystic fibrosis: A controlled study , 1985, Pediatric pulmonology.
[108] B. Joos,et al. Ciprofloxacin-induced hematuria , 1985, Infection.
[109] R. Stern,et al. Imipenem/cilastatin in acute pulmonary exacerbations of cystic fibrosis. , 1985, Reviews of infectious diseases.
[110] J. Ledbetter,et al. Comparison of cefoperazone sodium vs methicillin, ticarcillin, and tobramycin in treatment of pulmonary exacerbations in patients with cystic fibrosis. , 1985, The Journal of pediatrics.
[111] C. Buchanan,et al. Treatment of lower respiratory tract infections due to Pseudomonas aeruginosa in patients with cystic fibrosis. , 1984, Reviews of infectious diseases.
[112] J. van der Laag,et al. Piperacillin and tobramycin in the treatment of Pseudomonas lung infections in cystic fibrosis. , 1983, The Journal of antimicrobial chemotherapy.
[113] H. Levison,et al. Efficacy of inhaled tobramycin in the treatment of pulmonary exacerbations in children with cystic fibrosis , 1983, Pediatric infectious disease.
[114] E. Mellits,et al. A double-blind controlled trial of anti-Pseudomonas chemotherapy of acute respiratory exacerbations in patients with cystic fibrosis. , 1981, The Journal of pediatrics.
[115] G. Mccracken,et al. Acute Pulmonary Exacerbations in Cystic Fibrosis A Double-blind Trial of Tobramycin and Placebo Therapy , 1980 .
[116] C. Anderson,et al. Gentamicin and tobramycin compared in the treatment of mucoid pseudomonas lung infections in cystic fibrosis. , 1980, Archives of disease in childhood.
[117] R. Kraemer,et al. RELATIVE UNDERWEIGHT IN CYSTIC FIBROSIS AND ITS PROGNOSTIC VALUE , 1978, Acta paediatrica Scandinavica.
[118] J. Davies,et al. Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor. , 2018, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[119] Draft Guidance. Multiple Endpoints in Clinical Trials Guidance for Industry , 2017 .
[120] V. Waters,et al. Combination antimicrobial susceptibility testing for acute exacerbations in chronic infection of Pseudomonas aeruginosa in cystic fibrosis. , 2015, The Cochrane database of systematic reviews.
[121] I. Abdulhamid,et al. Hepatotoxicity induced by trimethoprim-sulfamethoxazole in a child with cystic fibrosis. , 2014, The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG.
[122] M. Walshaw,et al. Nebulized tobramycin in the treatment of adult CF pulmonary exacerbations. , 2014, Journal of aerosol medicine and pulmonary drug delivery.
[123] C. Wainwright,et al. Bronchoscopy-guided antimicrobial therapy for cystic fibrosis. , 2013, The Cochrane database of systematic reviews.
[124] A. Smyth,et al. Once-daily versus multiple-daily dosing with intravenous aminoglycosides for cystic fibrosis. , 2012, The Cochrane database of systematic reviews.
[125] A. Horsley,et al. Antibiotic treatment for Burkholderia cepacia complex in people with cystic fibrosis experiencing a pulmonary exacerbation. , 2012, The Cochrane database of systematic reviews.
[126] V. Waters,et al. Standard versus biofilm antimicrobial susceptibility testing to guide antibiotic therapy in cystic fibrosis. , 2020, The Cochrane database of systematic reviews.
[127] M. Hodson,et al. Twice vs three-times daily antibiotics in the treatment of pulmonary exacerbations of cystic fibrosis. , 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[128] D. Bilton,et al. Evaluation of Once Daily Tobramycin Versus the Traditional Three Time Daily for the Treatment of Acute Pulmonary Exacerbations in Adult Cystic Fibrosis Patients , 2006 .
[129] J. Elborn,et al. A comparison of pulmonary exacerbations with single and multiple organisms in patients with cystic fibrosis and chronic Burkholderia cepacia infection. , 2003, The Journal of infection.
[130] R. Echols,et al. Sequential ciprofloxacin therapy in pediatric cystic fibrosis: comparative study vs. ceftazidime/tobramycin in the treatment of acute pulmonary exacerbations. The Cystic Fibrosis Study Group. , 1997, The Pediatric infectious disease journal.
[131] K. De Boeck,et al. Treatment of Pseudomonas lung infection in cystic fibrosis with piperacillin plus tobramycin versus ceftazidime monotherapy: Preliminary communication , 1989, Pediatric pulmonology.
[132] B. Strandvik,et al. Comparison of efficacy and tolerance of intravenously and orally administered ciprofloxacin in cystic fibrosis patients with acute exacerbations of lung infection. , 1989, Scandinavian journal of infectious diseases. Supplementum.
[133] J. Blumer,et al. Comparison of piperacillin alone versus piperacillin plus tobramycin for treatment of respiratory infections in children with cystic fibrosis , 1988, Pediatric pulmonology.
[134] M. Corey,et al. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. , 1988, Journal of clinical epidemiology.
[135] D. Goldmann,et al. Randomized, double-blind evaluation of azlocillin for the treatment of pulmonary exacerbations of cystic fibrosis. , 1983, The Journal of antimicrobial chemotherapy.