Clostridium Difficile Infection in Adults Treatment and Prevention

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Clostridium Difficile Infection in Adults Treatment and Prevention Definition: Clostridium Difficile colonizes the human intestinal tract after the normal gut flora has been altered by antibiotic therapy and causes antibiotic-associated colitis. Risk factors: Antibiotic use is the most widely recognized and modifiable risk factor for Clostridium difficile. Age > 65 year. Recent hospitalization. Clinical manifestations: 1. Nonsevere CDI include watery diarrhea ( 3 loose stools in 24 hours) with lower abdominal pain and cramping, low-grade fever, and leukocytosis. * Criteria proposed for nonsevere CDI (based on expert opinion) include white blood cell count 15,000 cells/ml and serum creatinine <1.5 mg/dl; prospectively validated severity scores for CDI are needed. 2. Severe CDI include diarrhea, severe lower quadrant or diffuse abdominal pain, abdominal distention, fever, hypovolemia, lactic acidosis, hypoalbuminemia, and marked leukocytosis. * Criteria proposed for severe CDI (based on expert opinion) include white blood cell count >15,000 cells/ml and/or serum creatinine 1.5 mg/dl. 3. Fulminant colitis (severe, complicated CDI) may be characterized by hypotension or shock, ileus, or megacolon.

4. Recurrent C. difficile infection is defined by resolution of CDI symptoms while on appropriate therapy, followed by reappearance of symptoms within two to eight weeks after treatment has been stopped. Diagnosis: The diagnosis of C. difficile infection is established via a positive stool test for C. difficile toxin(s) or C. difficile toxin gene Laboratory testing should be pursued only in patients with clinically significant diarrhea, since testing cannot distinguish between CDI and asymptomatic carriage (which does not warrant treatment). For patients with ileus, laboratory diagnosis via perirectal swab for toxin assay or anaerobic culture may be performed. Radiographic imaging of the abdomen and pelvis is warranted for patients with clinical manifestations of severe illness or fulminant colitis to evaluate for presence of toxic megacolon, bowel perforation, or other findings warranting surgical intervention. Lower gastrointestinal endoscopy is not warranted in patients with typical clinical manifestations of C. difficile infection, a positive laboratory test, and/or clinical response to empiric treatment. In general, endoscopy may be pursued for circumstances in which an alternative diagnosis is suspected that requires direct visualization and/or biopsy of the bowel mucosa. It may also be helpful for patients with ileus or fulminant colitis in the absence of diarrhea since it may allow visualization of pseudomembranes (severe inflammation of the inner lining of the bowel), a finding that is highly suggestive of C. difficile infection. GENERAL PRINCIPLES Antibiotic management An important initial step in the treatment of CDI is discontinuation of the inciting antibiotic agent(s) as soon as possible.treatment with concomitant antibiotics (i.e., antibiotics other than those given to treat C. difficile infection) is associated with prolongation of diarrhea, increased likelihood of treatment failure, and increased risk of recurrent CDI.If ongoing antibiotics are essential for treatment of the primary infection, if possible, it may be prudent to select antibiotic agents that are less frequently implicated in antibiotic-associated CDI

Infection control Patients with suspected or proven C. difficile infection should be placed on contact precautions, and health care workers should wash hands before and after patient contact. Hand hygiene with soap and water may be more effective than alcohol-based hand sanitizers in removing C. difficile spores, since C. difficile spores are resistant to killing by alcohol. Diarrhea management In addition, antimotility agents such as loperamide and opiates have traditionally been avoided in CDI, but the evidence that they cause harm is equivocal. Supportive care with attention to correction of fluid losses and electrolyte imbalances is also important. Patients may have regular diet as tolerated PREVENTION Initial episode Strategies for preventing an initial episode of C. difficile infection include: Minimizing antibiotic use. Avoiding gastric acid suppression. Use of probiotics in some circumstances. Recurrent episode Strategies for preventing a recurrent episode of C. difficile infection include those summarized above for preventing an initial episode of CDI. Additional strategies include: secondary prophylaxis during concomitant antibiotic use In patients with a recent history of CDI who require systemic antibiotic therapy, secondary prophylaxis with oral vancomycin may reduce the likelihood of CDI recurrence. The optimal dose of oral vancomycin for secondary prophylaxis is uncertain; reasonable regimens may consist of standard dosing (125 mg orally four times daily) or reduced dosing (125 to 250 mg twice

daily).metronidazole should not be used for secondary prophylaxis because of its dosedependent association with peripheral neuropathy. Monoclonal antibodies Adjunctive use of monoclonal antibodies against C. difficile toxin may reduce the recurrence rate of C. difficile infection. Bezlotoxumab (a monoclonal antibody that binds to C. difficile toxin B) received US Food and Drug Administration approval in 2016 for secondary prevention of C. difficile infection in patients at high risk for recurrence (including patients >65 years of age and those with a prior history of CDI). Gastrointestinal colonization by nontoxigenic C. difficile strains Gastrointestinal colonization by nontoxigenic C. difficile strains has been shown to prevent CDI with exposure to a toxigenic.

Treatment

References: Lamont, J., Kelly,C., & Bakken, J. (2018), Clostridium difficile infection in adults: Clinical manifestations and diagnosis. E. L. Baron (Ed.), UpToDate.Retrieved October 8, 2018,from,https://www.uptodate.com/contents/clostridium-difficile-infection-inadults-clinical-manifestations-and-diagnosis Prepared by Pharm D students: 1) Saja Said. 2) Basma Abu Odeh. Supervised by clinical pharmacist: Eshraq Al-abweeny.