Effect Study of Tigecycline to Treat Severe Sepsis and Septic Shock (Tigecycline)
Abdominal Infection
About this trial
This is an interventional treatment trial for Abdominal Infection focused on measuring sepsis shock, Tigecycline, Piperacillin / tazobactam, Abdominal infection
Eligibility Criteria
Inclusion Criteria:
- Be consistent with severe sepsis and septic shock diagnosis standards
- Age above 18 years old, is expected in more than 5 days in ICU
- APACHEⅡ score>15
- By the patients themselves or their authorized person agreed to participate in the clinical trial and signed the informed consent
Exclusion Criteria:
- Allergic to penicillin, or of tigecycline allergic patients
- Patients with abnormal liver function is severe
- Be pregnant or lactating women
- Be not signed the informed consent of patients
- Any can be expected to increase patient risk or other factors can interfere with the results of a clinical trial
Sites / Locations
- TianjinCIHRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
glycopeptide plus carbapenem
Haizheng Li Xing ® plus tazocin ®
The control group antibiotic selection according to the classical scheme use of glycopeptide plus carbapenem antibiotic (or oxazolidinone antibiotics), with or without antifungal therapy, dose of imipenem/cilastatin 500mg, IVdrip, 3~4 times/d, or meropenem 1g, IVdrip, 3 times/d; vancomycin for 15mg/kg,2 times/d, or linezolid 300mg, IVdrip, 2 times/d; these drugs are required to state organ function in patients with drug doses adjustment, treatment for 3-5 days.
Tigecycline (Haizheng Li Xing ®) combined with piperacillin / tazobactam (tazocin ®), with or without antifungal therapy, dose of tigecycline first dose 100 mg, 50 mg, every 12 hours, piperacillin / tazobactam 4.5g, ivdrip, 3-4 times a day, each time the infusion of 3 hours, treatment for 3-5 days.