Reference
Sanders, Don B, et al. “Predictors of Pulmonary Exacerbation Treatment in Cystic Fibrosis”. J. Cyst. Fibros., vol. 19, no. 3, May 2020, pp. 407–414.
Abstract
BACKGROUND: Most studies of pulmonary exacerbations (PEx) in
cystic fibrosis (CF) focus on intravenous (IV)-treated PEx,
though most PEx are treated with oral antibiotics. Our
objectives were to describe predictors of antibiotic choice and
outcomes for PEx initially identified in clinic. METHODS: For
each patient in the U.S. CF Foundation Patient Registry, we
selected the first PEx recorded at a clinic visit in 2013-14
following a clinic visit without a PEx. We used multivariable
logistic regression to determine associations between clinical
characteristics and antibiotic treatment choice. We determined
outcomes in the 90 days after the first PEx. RESULTS: Among
14,265 patients with a PEx initially identified in clinic,
21.4% received no antibiotics, 61.5% received new oral and/or
inhaled antibiotics, and 17.0% had IV antibiotics within 14
days. Compared to IV antibiotics, patients more likely to
receive new oral and/or inhaled antibiotics: were male, 10th
percentile or 18.5 kg/m2, >90 days between clinic visits, FEV1 >
70% predicted at the PEx, no prior-year IV-treated PEx, FEV1
decline <10% predicted, and private insurance. Following the
PEx, 30.3% of patients had no clinical encounters within 90
days. Treatment with IV antibiotics within 90 days occurred for
23.7% treated without antibiotics, 22.8% of new oral and/or
inhaled antibiotics, and 27.1% of IV antibiotics. CONCLUSION:
Most PEx identified in clinic are treated with new oral and/or
inhaled antibiotics. Markers of disease severity are associated
with antibiotic treatment choice. Many patients had no follow-up
evaluation within 90 days of treatment.