July 13, 2011
Invasive Diagnostic Procedure for Cystic Fibrosis Does Not Improve Outcomes
(Ivanhoe Newswire) "“ Compared to standard diagnostic procedure, infants with cystic fibrosis who received treatment based on a diagnostic procedure involving gathering and culturing fluid samples from the lungs didn't have a lower prevalence of lung-damaging infection or structural lung injury at 5 years of age, according to this study.
Early pulmonary infection in children with cystic fibrosis, particularly with Pseudomonas aeruginosa, is associated with an increased risk of illness and death. Bronchoalveolar lavage (BAL) is an alternative diagnostic tool used when young children with cystic fibrosis cannot provide saliva, but evidence for its clinical benefit is lacking, according to background information in the article. BAL is a medical procedure in which a bronchoscope is passed through the mouth or nose into the lungs and fluid is instilled into a small part of the lung and then recollected for examination.Claire E. Wainwright, M.B.B.S., M.D., of the Royal Children's Hospital, University of Queensland, Brisbane, Australia, and colleagues conducted a study to examine whether BAL-directed therapy for pulmonary exacerbations in the first 5 years of life in infants with cystic fibrosis reduced P aeruginosa infection and structural lung injury at age 5. The randomized controlled trial included infants diagnosed with cystic fibrosis through newborn screening programs in 8 Australasian cystic fibrosis centers. Recruitment occurred between June 1999 and April 2005.
Participants received BAL-directed (n = 84) or standard (n = 86) therapy (based on oropharyngeal [pertaining to the mouth and the pharynx] cultures) until age 5 years. The BAL-directed therapy group underwent BAL before age 6 months when well, when hospitalized for pulmonary exacerbations, if P aeruginosa was detected in oropharyngeal specimens, and after P aeruginosa eradication therapy. Treatment was prescribed according to BAL or oropharyngeal culture results. Primary outcomes at age 5 years were prevalence of P aeruginosa on BAL cultures in both the BAL-directed and standard therapy groups and total cystic fibrosis computed tomography (CF-CT) score (as a percentage of the maximum score) on high-resolution chest CT scan.
Of 267 infants diagnosed with cystic fibrosis following newborn screening, 170 were enrolled and randomized and 157 completed the study. No statistically significant between-group differences for either of the primary outcomes were detected. P aeruginosa infection diagnosed by BAL culture was detected in 8/79 (10 percent) in the BAL-directed therapy group vs. 9/76 (12 percent) in the standard therapy group. For the outcome of total CF-CT score, data were obtained in 76 children (90 percent) in both study groups. The average total CF-CT scores for the BAL-directed therapy and standard therapy groups were 3.0 percent and 2.8 percent, respectively.
"This study highlights the importance of examining diagnostic and management interventions using appropriately designed randomized controlled trials in a clinical practice setting. BAL-directed therapy provided no clinical, microbiologic, or radiographic advantage and led to an increased risk of predominantly mild adverse events as a direct result of bronchoscopy as well as disadvantages such as the need to fast prior to the procedure, exposure to anesthesia, and potential perioperative anxiety. BAL remains a useful research tool in young, nonexpectorating children with cystic fibrosis. In clinical practice, however, BAL is perhaps best reserved for young children whose conditions are deteriorating despite parenteral [by injection, usually through the veins] antibiotic therapy, when unusual or antibiotic-resistant pathogens, including clonal P aeruginosa strains, are suspected, and to diagnose patients with chronic P aeruginosa infection," the authors were quoted as saying.
SOURCE: JAMA, published online July 13, 2011