Risk factors for recurrent melioidosis in northeast Thailand

被引:105
作者
Limmathurotsakul, Direk
Chaowagul, Wipada
Chierakul, Wirongrong
Stepniewska, Kasia
Maharjan, Bina
Wuthiekanun, Vanaporn
White, Nicholas J.
Day, Nicholas P. J.
Peacock, Sharon J.
机构
[1] Mahidol Univ, Fac Trop Med, Wellcome Unit, Bangkok 10400, Thailand
[2] Sappasithiprasong Hosp, Dept Med, Ubon Ratchathani, Thailand
[3] Univ Oxford, Churchill Hosp, Nuffield Dept Clin Med, Ctr Clin Vaccinol & Trop Med, Oxford, England
基金
英国惠康基金;
关键词
D O I
10.1086/507632
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Recurrent melioidosis occurs in similar to 6% of patients in the first year following the initial presentation. A recent study revealed that 25% of patients with recurrence had reinfection rather than a relapse resulting from a failure to cure. The aim of this study was to reevaluate these 2 patient groups to define their individual risk factors. Methods. All adult patients who presented to Sappasithiprasong Hospital (Ubon Ratchathani, in northeast Thailand) with culture-confirmed melioidosis during the period 1986-2004 and who survived to receive oral antimicrobial therapy were observed until July 2005. Clinical factors and antimicrobial treatment of patients with recurrent disease due to relapse or reinfection, as confirmed by bacterial genotyping, were compared using a time-varying Cox proportional hazard model. Results. Of 889 patients who survived and underwent follow-up, 86 patients (9.7%) presented with relapse, and 30 patients (3.4%) became reinfected. There was no difference in acute outcome between the relapse and reinfection groups. No risk factors for reinfection were identified. Multivariate analyses identified choice and duration of oral antimicrobial therapy as the most important determinants of relapse, followed by positive blood culture result ( hazard ratio [HR], 1.86; 95% confidence interval [CI], 1.18-2.92) and multifocal distribution ( HR, 1.95; 95% CI, 1.03-3.67). Patients treated with an appropriate oral antibiotic regimen for 12-16 weeks had a 90% decreased risk of relapse ( HR, 0.10; 95% CI, 0.02-0.44), compared with patients who were treated for <= 8 weeks. Trimethoprim-sulfamethoxazole plus doxycycline was an effective oral therapy. Conclusions. This study highlights clinical factors associated with an increased likelihood of relapse and provides evidence for optimal oral antimicrobial therapy.
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收藏
页码:979 / 986
页数:8
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