Study objectives: Patients with CORD are at risk of experiencing a deterior
ation in arterial oxygen saturation (SaO(2)) during sleep, which is general
ly most pronounced during rapid eye movement (REM) sleep. Increased choline
rgic tone has been suggested as a contributing factor to this decrease in S
aO(2), Therefore, we investigated whether 4-week treatment with ipratropium
bromide inhalation solution 0.02% (qid) could improve sleep characteristic
s in COPD,
Design: Randomized, placebo-controlled, double-blind, two-arm parallel stud
y of 4 weeks of treatment with ipratropium bromide solution or placebo.
Setting: Multicenter investigation.
Patients: Thirty-six patients with moderate-to-severe COPD (FEV1 < 65% of p
redicted). Measurements and results: Evaluation included polysomnographic,
pulmonary function, and subjective quality of sleep (visual analog scale [V
AS]) assessments. It was found that 4 week of treatment with ipratropium br
omide solution in patients with COPD led to the following: (1) a significan
t (p = 0.05) improvement in mean nocturnal SaO(2) with the more severe the
nocturnal desaturation, the greater the improvement in SaO(2); (2) signific
ant (p = 0.03) improvement in perceived sleep quality (VAS: 5.5 +/- 0.5 aft
er placebo; 7.2 +/- 0.5 after ipratopium); (3) a significant (p = 0.05) inc
rease in REM sleep time (48.6 +/- 6.3 min after placebo; 66.5 +/- 6.4 min a
fter ipratropium) with no effect on other sleep stages or total sleep time;
and (4) a significant (p = 0.01) increase in pre-sleep FVC and flow rate a
t 50% of the vital capacity.
Conclusions: These findings demonstrate that ipratropium bromide therapy ca
n improve sleep SaO(2) as well as sleep quality in patients with moderate-t
o-severe COPD.