Effect of erythromycin before endoscopy in patients presenting with variceal bleeding: a prospective, randomized, double-blind, placebo-controlled trial.
Аннотация
BACKGROUND
Blood in the stomach and esophagus in patients with variceal bleeding often obscures the endoscopic view and makes endoscopic intervention difficult to perform. Erythromycin, a motilin agonist, induces gastric emptying.
OBJECTIVE
To assess the effect of erythromycin on endoscopic visibility and its outcome in patients with variceal bleeding.
DESIGN
Randomized, double-blind, placebo-controlled trial.
SETTING
Tertiary care hospital.
PATIENTS: Adult patients with liver cirrhosis presenting with hematemesis within the previous 12 hours.
INTERVENTION: Either 125 mg erythromycin or placebo administered intravenously 30 minutes before endoscopy.
MAIN OUTCOME MEASUREMENTS: Endoscopic visibility during index endoscopy and mean duration of procedure. SECONDARY OUTCOME MEASUREMENTS: Need for repeat endoscopy and blood transfusions within 24 hours, endoscopy-related complications, and length of hospital stay.
RESULTS
A total of 102 patients received either erythromycin or placebo (53 erythromycin and 49 placebo). Forty-seven patients in the erythromycin group and 43 in the placebo group had variceal bleeding and were considered for final analysis. A completely empty stomach was seen in 48.9% of the erythromycin group versus 23.3% of the placebo group (P<.01). Mean endoscopy duration was significantly shorter in the erythromycin group than in the placebo group (19.0 minutes vs 26.0 minutes, respectively; P<.005). Length of hospital stay was significantly shorter in the erythromycin group than in the placebo group (3.4 days vs 5.1 days, respectively; P<.002). The need for repeat endoscopy and the mean number of units of blood transfused did not differ significantly in the 2 groups. No adverse events were observed with erythromycin.
LIMITATIONS: Sample size not sufficient to measure the need for repeat endoscopy and survival benefit.
CONCLUSIONS
Erythromycin infusion before endoscopy in patients with variceal bleeding significantly improves endoscopic visibility and shortens the duration of the index endoscopy. (
CLINICAL TRIAL REGISTRATION NUMBER: NCT01060267.).
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