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Meropenem monotherapy for the treatment of hospital-acquired pneumonia: results of a multicenter trial.

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.
AuthorsS J Berman, C M Fogarty, T Fabian, D Melnick, W Lesky, Merrem Hospital-Acquired Pneumonia Study Group
JournalJournal of chemotherapy (Florence, Italy) (J Chemother) Vol. 16 Issue 4 Pg. 362-71 (Aug 2004) ISSN: 1120-009X [Print] England
PMID15332712 (Publication Type: Clinical Trial, Comparative Study, Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)
Chemical References
  • Thienamycins
  • Meropenem
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

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