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Cefotaxime Resistance in Treatment of Spontaneous Bacterial Peritonitis

Not Applicable
Completed
Conditions
Spontaneous Bacterial Peritonitis
Interventions
Registration Number
NCT02388035
Lead Sponsor
Dr Ahmed Ali Elbaz
Brief Summary

Spontaneous bacterial peritonitis (SBP) is a serious complication in cirrhotic patients, and the changes in the microbiological characteristics reported in the last years are impacting the choice of antibiotic used in the treatment. Cefotaxime has been the most extensively studied antibiotic for this infection. It is considered to be one of the first choice antibiotics because of low toxicity and excellent efficacy. Treatment of SBP by intravenous cefotaxime should be administered for a minimum 5 days. Antibiotic-resistant microorganisms have been increasingly reported especially to cefotaxime and its effect on the clinical outcome in treating SBP.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
254
Inclusion Criteria
  • patients with liver cirrhosis and ascites and clinical findings suspicious of ascitic fluid infection
Exclusion Criteria
  • Patients were excluded if they received antibiotics ten days prior to the hospital admission or there is evidence of secondary bacterial peritonitis, tuberculous peritonitis, malignant ascites or ascites due to other causes e.g. cardiac or renal diseases

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CNNA-group 2CefotaximeCulture negative neutrocytic ascites
SBP-group 1CefotaximeSpontanous bacterial peritonitis
MNBA-group 3Cefotaximemonomicrobial non-neutrocytic ascites
Primary Outcome Measures
NameTimeMethod
Organisms detected with their antibiotics sensitivity8 months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Nasser institute

🇪🇬

Cairo, Shubra, Egypt

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