Short-Course Isoniazid Plus Rifapentine Directly Observed Therapy for Latent Tuberculosis in Solid-Organ Transplant Candidates

被引:29
|
作者
de Castilla, Diego Lopez [1 ]
Rakita, Robert M. [1 ]
Spitters, Christopher E. [1 ]
Narita, Masahiro [2 ]
Jain, Rupali [3 ]
Limaye, Ajit P. [1 ]
机构
[1] Univ Washington, Dept Med, Div Allergy & Infect Dis, Solid Organ Transplant Infect Dis Program, Seattle, WA 98195 USA
[2] Univ Washington, Dept Med, Div Pulm & Crit Care, Seattle, WA 98195 USA
[3] Univ Washington, Sch Pharm, Seattle, WA 98195 USA
关键词
Isoniazid; Rifapentine; Latent tuberculosis infection; Solid-organ transplantation; INFECTION; RECIPIENTS; RIFAMPIN; CHEMOPROPHYLAXIS; HEPATOTOXICITY; SAFETY; TRIAL; RISK;
D O I
10.1097/TP.0b013e3182a94a2f
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 Short-course directly observed isoniazid plus rifapentine (INH/RPT) combination could have potential advantages over a standard 9-month INH regimen for the treatment of latent tuberculosis infection in solid-organ transplant (SOT) candidates. Methods We prospectively assessed the safety and tolerability of 12 weeks of INH/RPT given directly observed therapy in 17 consecutive SOT candidates with latent tuberculosis infection. Results The median age was 57 years and 82% were men. Of the 17 patients, 13 (76%) successfully completed therapy and 4 (24%) eventually underwent SOT. Treatment was prematurely discontinued in four patients. One of these patients underwent a kidney transplant. The overall dose compliance was 83% (169/204 scheduled doses), and 12 (71%) of 17 patients received 100% of scheduled doses. No patient developed transaminase elevations greater than twice baseline or greater than four times the upper limit of normal or clinical hepatotoxicity. No cases of TB developed during 20.4 months after transplant among INH/RPT-treated recipients. Conclusions For carefully selected SOT candidates, combination INH/RPT weekly given as directly observed therapy seems to be reasonably well tolerated and is associated with a relatively high completion rate. Future larger prospective studies to confirm the safety and high completion rates reported here and to identify the most appropriate SOT candidates for this regimen are warranted.
引用
收藏
页码:206 / 211
页数:6
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