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Abstract

Vol.59 No.6 November 2011

Treatment strategy aimed towards for the short-term use of linezolid in severe and refractory infections with methicillin-resistant Staphylococcus aureus

Yoshiko Takahashi1), Yoshio Takesue1), Kazuhiko Nakajima1), Kaoru Ichiki1), Yasunao Wada1), Mika Ishihara2), Sumiyo Tatsumi2) and Takeshi Kimura2)

1)Department of Infection Control and Prevention, The Hospital of Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo, Japan
2)Department of Pharmacy, The Hospital of Hyogo College of Medicine

Abstract

Purpose: The restricted use of linezolid(LZD) is mandatory to prevent adverse effects and occurrence of resistance. The aim of the present study was to investigate the efficiency of a treatment strategy aimed at short-term LZD use in patients with methicillin-resistant Staphylococcus aureus(MRSA) infections.
Methods: This study was conducted between July 2007 and June 2009. The strategy was referred to as a scheduled sequential therapy(SST) consisted of step down therapy(SD) in severe infections and LZD use restricted to the peri-operative period in refractory infections (use restricted to the peri-operative period; URPOP).
Results: Seventy patients undergoing SST (28 patients for SD, 44 patients for URPOP, 2 patients were overlapped) were examined. The duration of LZD was 7.8±5.4 days in patients undergoing SST. The efficacy during the course of SST was 58/70 patients (82.9%) (SD 71.4%, URPOP 90.9%). The efficacy during LZD administration was 95.7% (SD 100%, URPOP 93.2%). The occurrence of thrombocytopenia in SST was 28.6% (SD 35.7%, URPOP 25.0%) and tended to be lower compared with that in LZD use for patients who did not undergo SST (p=0.051).
Conclusions: With SST, the duration of LZD use was about 8 days in patients with severe/refractory MRSA infections, and the implementation of SST was not only associated with a low incidence of thrombocytopenia but also showed a high efficacy rate.

Key word

linezolid, MRSA, sepsis, thrombocytopenia

Received

April 12, 2011

Accepted

July 22, 2011

Jpn. J. Chemother. 59 (6): 580-584, 2011