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PMID: 8574715 Published · ppublish English Clinical Trial Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Antibiotic prophylaxis for ERCP: a randomized clinical trial comparing ciprofloxacin and cefuroxime in 200 patients at high risk of cholangitis.

European journal of gastroenterology & hepatology ·Vol. 7 ·No. 9 ·1995-09-00 ·Pages 841-5

Mehal WZ, Culshaw KD, Tillotson GS, Chapman RW

Abstract

To compare the efficacy and safety of oral ciprofloxacin and intravenous cefuroxime in patients at high risk of cholangitis after endoscopic retrograde cholangiopancreatography (ERCP). Prospective, randomized study. A primary and tertiary referral centre. A series of 232 consecutive patients who either had radiological evidence of biliary obstruction or were aged over 70 years were randomly assigned to receive either oral ciprofloxacin or intravenous cefuroxime before and after ERCP. Two-hundred and nine patients finished the study, with 23 being excluded because of withdrawal of consent or incomplete ERCP. Patients underwent ERCP: blood samples were taken for culture, full blood count and biochemistry before and after the procedure. Clinical follow-up was carried out 7 and 42 days after ERCP. Clinical, bacteriological or biochemical evidence of cholangitis, septicaemia or adverse drug reactions, and the cost of both protocols. Follow-up was recorded in all 209 patients who completed the study. By 42 days after ERCP, three patients had died (cholangiocancer, pancreatic cancer and renal failure). Cholangitis was diagnosed in one patient from each of the two trial groups. Blood cultures from the patient on ciprofloxacin gave negative results, but a post-ERCP blood sample from the patient on cefuroxime grew Pseudomonas aeruginosa, which was sensitive to ciprofloxacin. There were no serious side-effects in either study group, but two patients assigned to ciprofloxacin became too nauseous to take the medication. The cost of the cefuroxime protocol was l7.56 pounds per patient, compared with 4.76 pounds per patient for the ciprofloxacin protocol. A pre- and post-ERCP oral ciprofloxacin regime is safe and provides effective prophylaxis against ERCP-induced cholangitis and septicaemia in high-risk patients. It is also more economical than a regime of intravenous cefuroxime and does not require nursing staff with training in intravenous techniques.

MeSH Terms
Adult Aged Anti-Infective Agents/administration & dosage,economics,therapeutic use Antibiotic Prophylaxis/economics Cefuroxime/administration & dosage,economics,therapeutic use Cephalosporins/administration & dosage,economics,therapeutic use Cholangiopancreatography, Endoscopic Retrograde/adverse effects Cholangitis/prevention & control Ciprofloxacin/administration & dosage,economics,therapeutic use Drug Therapy, Combination Female Follow-Up Studies Humans Male Middle Aged Prospective Studies Risk Factors
Chemicals
Anti-Infective Agents Cephalosporins Ciprofloxacin Cefuroxime
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Mehal W Z
Department of Gastroenterology, John Radcliffe Hospital, Oxford, UK.
Culshaw K D
Tillotson G S
Chapman R W
Article Info
Journal
European journal of gastroenterology & hepatology
Abbr.
Eur J Gastroenterol Hepatol
ISSN
0954-691X
Published
1995-09-00
Pages
841-5
Language
English
Region
England
NLM ID
9000874
Subset
IM
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