Defining a pulmonary exacerbation in cystic fibrosis.

OBJECTIVES Despite the central importance of pulmonary exacerbations (PExs) as an outcome measure in cystic fibrosis clinical trials, no standardized definition of PEx exists. We conducted a prospective, multicenter study to establish a standardized PEx definition and score for use in clinical trials, based on clinical status rather than on treatment decisions. STUDY DESIGN Subjects were 246 patients enrolled in the placebo arm of a randomized, controlled trial of tobramycin for inhalation. Physician-investigators completed PEx questionnaires on all subjects at scheduled intervals during the 6-month study, indicating new or worsening symptoms, physical examination findings, and impression of PEx status (presence or absence and severity). Logistic regression was used to assess the relative importance of each of the characteristics in predicting a PEx. RESULTS We developed 2 PEx scores that use easily ascertained symptoms and chest examination findings; one also includes change in forced expiratory volume in 1 second over the preceding month. Both scores were sensitive and specific for predicting the presence of a PEx (sensitivity, 86%; specificity, 86%). The scores were validated in subjects in the intervention arm of the trial. CONCLUSION We hope that the proposed PEx score might serve as a standardized outcome measure for future clinical trials in cystic fibrosis, allowing meaningful comparisons of study results.

[1]  M S Pepe,et al.  Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group. , 1999, The New England journal of medicine.

[2]  D. Turck,et al.  Efficacy, tolerance, and pharmacokinetics of once daily tobramycin for pseudomonas exacerbations in cystic fibrosis , 1998, Archives of disease in childhood.

[3]  B. Ramsey,et al.  Management of pulmonary disease in patients with cystic fibrosis. , 1996, The New England journal of medicine.

[4]  P. J. Byard,et al.  Effect of high-dose ibuprofen in patients with cystic fibrosis. , 1995, The New England journal of medicine.

[5]  H. Fuchs,et al.  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, The New England journal of medicine.

[6]  T. Boat,et al.  Outcome measures for clinical trials in cystic fibrosis. Summary of a Cystic Fibrosis Foundation consensus conference. , 1994, The Journal of pediatrics.

[7]  D. Gozal,et al.  Evolution of pulmonary function during an acute exacerbation in hospitalized patients with cystic fibrosis , 1993, Pediatric pulmonology.

[8]  E. Valletta,et al.  Modification of some markers of inflammation during treatment for acute respiratory exacerbation in cystic fibrosis , 1992, Acta paediatrica.

[9]  R. Cowan,et al.  Intravenous immune globulin treatment of pulmonary exacerbations in cystic fibrosis. , 1989, The Journal of pediatrics.

[10]  G. Redding,et al.  Sputum changes associated with therapy for endobronchial exacerbation in cystic fibrosis. , 1988, The Journal of pediatrics.

[11]  R. Wood,et al.  What is a "pulmonary exacerbation" incystic fibrosis? , 1987 .

[12]  R. Stern,et al.  Ceftazidime therapy in patients with cystic fibrosis and multiply-drug-resistant pseudomonas. , 1985, The American journal of medicine.

[13]  J. Nelson Management of acute pulmonary exacerbations in cystic fibrosis: a critical appraisal. , 1985, The Journal of pediatrics.

[14]  F. Granata,et al.  Ceftazidime in treatment of acute pulmonary exacerbations in patients with cystic fibrosis. , 1983, The Journal of pediatrics.

[15]  D. Goldmann,et al.  Clinical and bacteriological responses to three antibiotic regimens for acute exacerbations of cystic fibrosis: ticarcillin-tobramycin, azlocillin-tobramycin, and azlocillin-placebo. , 1983, The Journal of infectious diseases.

[16]  G. Cabrini,et al.  Alternative antibiotics for the treatment of Pseudomonas infections in cystic fibrosis. , 1983, The Journal of antimicrobial chemotherapy.

[17]  G. Redding,et al.  Serial changes in pulmonary functions in children hospitalized with cystic fibrosis. , 1982, The American review of respiratory disease.

[18]  M. Marks,et al.  Is anti-Pseudomonas therapy warranted in acute respiratory exacerbations in children with cystic fibrosis? , 1980, The Journal of pediatrics.

[19]  S. Soong,et al.  The chest roentgenogram in cystic fibrosis: a new scoring system. , 1979, Pediatrics.

[20]  R. Kraemer,et al.  Relationship between clinical conditions, radiographic findings and pulmonary functions in patients with cystic fibrosis. , 1979, Helvetica paediatrica acta.

[21]  J. Kattwinkel,et al.  A new prognostic score and clinical evaluation system for cystic fibrosis. , 1973, The Journal of pediatrics.

[22]  H. Shwachman,et al.  Long-term study of one hundred five patients with cystic fibrosis; studies made over a five- to fourteen-year period. , 1958, A.M.A. journal of diseases of children.