Diarrhoea is a common adverse effect of antibiotic treatments. Antibiotic
associated diarrhoea occurs in about 5-30% of patientseither early
during antibiotic therapy or up to two months afterthe end of the
treatment.1-3 The frequency of antibiotic
associateddiarrhoea depends on the definition of diarrhoea, the
incitingantimicrobial agents, and hostfactors.
Almost all antibiotics, particularly those that act on anaerobes, can cause
diarrhoea, but the risk is higher with aminopenicillins,a
combination of aminopenicillins and clavulanate, cephalosporins,and
clindamycin. 145 Host factors for antibiotic associated
diarrhoea include age over 65, immunosuppression, being in an
intensive care unit, and prolonged hospitalisation.6
Clinical presentations of antibiotic associated diarrhoea range from mild
diarrhoea to fulminant pseudomembranous colitis.The latter is
characterised by a watery diarrhoea, fever (in 80%of cases),
leucocytosis (80%), and the presence of pseudomembraneson endoscopic
examination. Severe complications include toxicmegacolon,
perforation, andshock.
Antibiotic associated diarrhoea results from disruption of the normal
microflora of the gut by antibiotics. This microflora,composed of 1011
bacteria per gram of intestinal content, forms a stable ecosystem
that permits the elimination of exogenous organisms. Antibiotics
disturb the composition and the function of this flora and enable
overgrowth of micro-organisms that induce diarrhoea. Since demonstrationof its role in 1978, Clostridium difficile has emerged as themajor enteropathogen of antibiotic associated diarrhoea.3
Thisanaerobic spore forming bacteria is responsible for 10-25% ofcases of antibiotic associated diarrhoea and for virtually all
cases of pseudomembranous colitis.3 It works by
secreting twopotent toxins that cause mucosal damage and
inflammation of thecolon. Other infectious agents reported to be
responsible forantibiotic associated diarrhoea include C
perfringens, Staphylococcusaureus, Candida spp,
Klebsiella oxytoca, and Salmonella spp.7However, their role in the pathogenesis of diarrhoea is still
debated because most of them are considered to be usual commensal
bacteria of the gut flora. Antibiotic associated diarrhoea canalso
result from a decrease in metabolism of carbohydrates andbile acids.7
Managing the diarrhoea depends on the clinical presentation and the inciting
agent.7-10 In mild to moderate diarrhoea
conventionalmeasures include rehydration or discontinuation of the
incitingagent or its replacement by an antibiotic with a lower risk
ofinducing diarrhoea, such as quinolones, co-trimoxazole, or
aminoglycosides.In 22% of cases of diarrhoea related to C
difficile, withdrawalof the inciting agent will lead to
resolution of clinical signsin three days.11
In cases of severe or persistent antibiotic associated diarrhoea, the
challenge is to identify C difficile associated infections
since this is the most common identifiable and treatable pathogen.
Diagnosis relies on detecting toxins A or B in stools. Tissueculture
assay is the gold standard, although it is time consuming.Enzyme
immunoassays for toxins A or B have a good specificitybut a false
negative rate of 10-20%.
Treatment of C difficile related diarrhoea is based on oral
metronidazole (250 mg four times daily) or oral vancomycin (125mg
four times daily) for 10 days. 1112 The response to metronidazoleor vancomycin is
similar (>90%), and diarrhoea usually resolvesin two or three days.
The Infectious Diseases Society of America,the American College of
Gastroenterology, and the Society forHospital Epidemiology of
America recommend metronidazole as thefirst line of treatment to
prevent the emergence of vancomycinresistant organisms.
910 Vancomycin
should be reserved forthose with severe illness, intolerance to
metronidazole, failureto respond to metronidazole, or pregnancy.
Antiperistaltic agentsshould be avoided because of the risk of
retention of toxins inthe lumen. About 20% of patients with C
difficile related diarrhoeawill relapse. Most patients will
respond to another course ofmetronidazole or vancomycin, but 5% will
experience several relapses;the management of these remainscontroversial.
As antibiotic associated diarrhoea mostly results from a disequilibrium of
the normal intestinal flora, research has focusedon the benefits of
administering living organisms (probioticsor biotherapeutic agents)
to restore the normal flora. Numerousprobiotics such as
Lactobacillus acidophilus, L casei GG, L bulgaricus,Bifidobacterium bifidum, B longum, Enterococcus faecium,
Streptococcusthermophilus, or Saccharomyces boulardii
have been tested forthe treatment and prevention of antibiotic
associated diarrhoea.13The benefits of
probiotics are unproved as few have been evaluatedin double blind
placebo controlled studies. The results of thesmall and open trials
of treatment areconflicting.
Most studies with probiotics have assessed their use in preventing antibiotic
associated diarrhoea. In this issue D'Souzaet al report a
meta-analysis of nine randomised double blind trialscomparing
probiotics with placebo in the prevention of diarrhoea(p 1361).14
Among these studies, four trials were used S boulardiiand
five Lactobacillus. Their results suggest that probioticsare
useful in prevention. The expected advantages of probioticsinclude
ease of administration, cost effectiveness, and relativelack of side
effects. However, several cases of bacteraemia withS boulardii
have been reported, which should prompt caution inthe use of
this yeast in immunosuppressed patients or patientswith underlyingdisorders.
The key measure for preventing antibiotic associated diarrhoea, however, is
to limit antibiotic use. Probiotics have proveduseful in preventing
diarrhoea, but the number of clinical trialsis limited and further
controlled trials using different probioticsare needed. In the case
of C difficile related diarrhoea hygienemeasures (single
rooms, use of gloves, and handwashing) shouldbe systematically
associated with treatment in order to preventtransmission and
dissemination of this nosocomialbacteria.
Frédéric Barbut, head of infection control.
Unité d'Hygiène et de Lutte contre l'Infection Nosocomiale (UHLIN), Hôpital
Saint-Antoine, 75 571 Paris cedex 12, France (frederic.barbut@sat.ap-hop-paris.fr)
Jean Luc Meynard, senior research fellow in
infectious diseases.
Bartlett JG, Chang TW, Gurwith M, Gorbach SL, Onderdonk AB.
Antibiotic-associated pseudomembranous colitis due to toxin producing
Clostridia. N Engl J Med 1978; 298: 531-534[Abstract].
McFarland LV, Surawicz CM, Stamm WE. Risk factors for
Clostridium difficile carriage and C. difficile-associated diarrhea in a
cohort of hospitalized patients. J Infect Dis 1990; 162: 678-684[Medline].
Fekety R. Guidelines for the diagnosis and management of
Clostridium difficile-associated diarrhea and colitis. Am J Gastroenterol
1997; 92: 739-750[Medline].
Fekety K, Silva J, Kauffman C, Scarpellini P, Rigoli R,
Manfrin V, et al. Treatment of Clostridium difficile associated colitis with
oral vancomycin: comparison of two dosage regimens. Am J Med 1989;
86: 15-19.
Marteau PR, de Vrese M, Cellier CJ, Schrezenmeir J.
Protection from gastrointestinal diseases with the use of probiotics. Am
J Clin Nut 2001; 73 (suppl): 4306-S.
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