Abstract | OBJECTIVE: METHODS: An open, perspective, multicenter clinical trial was conducted. Among the enrolled 665 patients, 621 patients with moderate to severe pulmonary infection were treated with intravenous panipenem-betamipron at a dose of 500 mg every 6 hours per day for 7 - 14 days. Among them, the community acquired pneumonia (CAP), hospital acquired pneumonia (HAP) and ventilator associated pneumonia (VAP) patients were 55.6% (345/621), 37.0% (230/621) and 7.4% (46/621), respectively. All the adverse events were recorded. RESULTS: The overall effective rate of panipenem-betamipron was 84.4% with CAP of 91.9%, HAP of 76.1% and VAP of 69.6%. The effective rates in the patients with moderate and severe pulmonary infection were 87.5% and 82.8%, respectively. Bacterial separation rate was 54.8% and bacterial eradication rate was 80.9%. Bacterial eradication rates to pseudomonas aeruginosa, pneumobacillus, Escherichia coli. and acinetobacter baumannii were 74.7%, 95.6%, 89.5% and 50.9%, respectively. The adverse events rate was 1.8% (12/665). CONCLUSION:
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Authors | Clinical Trial Research Group on Panipenem-betamipron |
Journal | Zhonghua nei ke za zhi
(Zhonghua Nei Ke Za Zhi)
Vol. 51
Issue 7
Pg. 547-50
(Jul 2012)
ISSN: 0578-1426 [Print] China |
PMID | 22943829
(Publication Type: English Abstract, Journal Article, Multicenter Study)
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Chemical References |
- Anti-Bacterial Agents
- Thienamycins
- beta-Alanine
- panipenem-betamipron
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Topics |
- Adult
- Aged
- Anti-Bacterial Agents
(adverse effects, therapeutic use)
- Community-Acquired Infections
(drug therapy)
- Cross Infection
(drug therapy)
- Drug Therapy, Combination
- Female
- Humans
- Male
- Middle Aged
- Pneumonia, Bacterial
(drug therapy)
- Prospective Studies
- Thienamycins
(adverse effects, therapeutic use)
- Treatment Outcome
- beta-Alanine
(adverse effects, analogs & derivatives, therapeutic use)
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