Antibiotic susceptibility of Burkholderia pseudomallei from tropical northern Australia and implications for therapy of melioidosis

被引:106
作者
Jenney, AWJ
Lum, G
Fisher, DA
Currie, BJ
机构
[1] Menzies Sch Hlth Res, Darwin, NT 0810, Australia
[2] Royal Darwin Hosp, Infect Dis Unit, Darwin, NT 0810, Australia
[3] Royal Darwin Hosp, Dept Pathol, Darwin, NT 0810, Australia
[4] No Terr Clin Sch, Darwin, NT 0810, Australia
关键词
melioidosis study; Burkholderia pseudomallei; culture positive infections;
D O I
10.1016/S0924-8579(00)00334-4
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
From a prospective melioidosis study commencing in 1989 at Royal Darwin Hospital, 170 initial isolates of Burkholderia pseudomallei were available for susceptibility testing. Of these 163 (96%) were susceptible to meropenem/imipenem, ceftazidime, trimethoprim-sulphamethoxazole (SMX/TMP) and doxycycline. Seven (4%) showed primary resistance; three had low-level resistance to SMX/TMP, one to ceftriaxone and amoxycillin/clavulanate (AMOX/CA) and three to doxycycline. Of 167 patients who survived their initial presentation, seven (4%,) had culture positive infections which persisted for greater than 3 months after start of therapy. All ultimately cleared carriage of B. pseudomallei though three required changing to SMX/TMP after development of doxycycline resistance. Nineteen (11%) of the initial survivors clinically relapsed and 17 of these had repeat isolates available for testing. Four of these had acquired resistance: one to doxycyline, one to AMOX/CA and ceftazidime, one to SMX/TMP and one to both SMX/TMP and doxycycline. Molecular typing using randomly amplified polymorphic DNA and pulsed-held gel electrophoresis showed all but one relapse isolate to be the same as the original strain. These data an similar to published data from Thailand. As melioidosis has a high mortality (21% in this series) these results emphasize the need for prolonged eradication therapy and regular clinical and microbiological monitoring so that the emergence of resistance can be detected early and appropriate treatment modifications made. (C) 2001 Elsevier Science B.V, and international Society of Chemotherapy. All rights reserved.
引用
收藏
页码:109 / 113
页数:5
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