Abstract |
The efficacy and tolerability of meropenem as empirical treatment in patients with hospital-acquired pneumonia was determined in a prospective, open-label, non-randomized trial. Patients from 28 centers in the USA received meropenem 1 g every 8 h intravenously. Of 255 patients enrolled, 111 were evaluable for efficacy, including 60 patients with ventilator-associated pneumonia. At end of treatment 74% of patients had a satisfactory clinical response and 64% had this response at follow-up, which could last up to 28 days after treatment. In patients with ventilator-associated pneumonia, a satisfactory clinical response was observed in 68% at the end of treatment and 63% at follow-up. The overall satisfactory response rate for individual pretreatment pathogens ranged from 65% to 100%. This study demonstrates that meropenem monotherapy is effective and well tolerated for patients with hospital-acquired pneumonia, including a subgroup of patients with ventilator-associated pneumonia.
|
Authors | S J Berman, C M Fogarty, T Fabian, D Melnick, W Lesky, Merrem Hospital-Acquired Pneumonia Study Group |
Journal | Journal of chemotherapy (Florence, Italy)
(J Chemother)
Vol. 16
Issue 4
Pg. 362-71
(Aug 2004)
ISSN: 1120-009X [Print] England |
PMID | 15332712
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)
|
Chemical References |
|
Topics |
- Adolescent
- Adult
- Aged
- Cross Infection
(drug therapy, microbiology)
- Dose-Response Relationship, Drug
- Drug Administration Schedule
- Female
- Follow-Up Studies
- Gram-Negative Bacterial Infections
(diagnosis, drug therapy)
- Gram-Positive Bacterial Infections
(diagnosis, drug therapy)
- Humans
- Infusions, Intravenous
- Male
- Meropenem
- Middle Aged
- Pneumonia, Bacterial
(drug therapy, microbiology)
- Probability
- Prospective Studies
- Respiration, Artificial
(adverse effects)
- Risk Assessment
- Thienamycins
(administration & dosage)
- Treatment Outcome
|