Jj. Smucny et al., Are beta(2)-agonists effective treatment for acute bronchitis or acute cough in patients without underlying pulmonary disease? A systematic review, J FAM PRACT, 50(11), 2001, pp. 945-951
OBJECTIVE our goal was to determine whether beta (2)-agonists improve the s
ymptoms of acute bronchitis or acute cough in patients who do not have unde
rlying pulmonary disease.
STUDY DESIGN We performed a systematic review including meta-analysis.
DATA SOURCES We included randomized controlled trials comparing beta (2)-ag
onists with placebo or alternative therapies identified from the Cochrane L
ibrary, MEDLINE, EMBASE, conference proceedings, Science Citation Index, th
e System for Information on Grey literature in Europe, and letters to manuf
acturers of beta (2)-agonists.
OUTCOME MEASURED We measured duration, persistence, severity or frequency o
f cough, productive cough, and night cough; duration of activity limitation
s; and adverse effects.
RESULTS Two trials in children with cough and no obvious airway obstruction
did not find any benefits from beta (2)-agonists. Five trials in adults wi
th cough and with or without airway obstruction had mixed results, but summ
ary statistics did not reveal any significant benefits from beta (2)-agonis
ts. Studies that enrolled more wheezing patients were more likely to show b
enefits from beta (2)-agonists, and in one study only patients with evidenc
e of airflow limitation were more likely to benefit, Patients given beta (2
)-agonists were more likely to report tremor, shakiness, or nervousness tha
n those in the control groups.
CONCLUSIONS There is no evidence to support using beta (2)-agonists in chil
dren with acute cough and no evidence of airflow obstruction. There is litt
le evidence that the routine use of beta (2)-agonists for adults with acute
cough is helpful. These agents may reduce symptoms, including cough, in pa
tients with evidence of airflow obstruction, but this potential benefit is
not well-supported by the available data and must be weighed against the ad
verse effects associated with beta (2)-agonists.