Kim Sung-Han, Lee Sang-Oh, Park In-Ah, Kim Sun-Mi, Park Su Jin, Yun Sung-Cheol, Jung Joo Hee, Shin Sung, Kim Young Hoon, Choi Sang-Ho, Kim Yang Soo, Woo Jun Hee, Park Su-Kil, Park Jung Sik, Han Duck Jong
Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea
J Antimicrob Chemother. 2015 May;70(5):1567-72. doi: 10.1093/jac/dku562. Epub 2015 Jan 20.
We performed a randomized trial of isoniazid treatment based on interferon-γ-releasing assay (IGRA) in kidney transplant (KT) recipients in an intermediate-TB-burden country.
All adult patients admitted to a KT institute between June 2010 and May 2013 were enrolled. The IGRA (T-SPOT.TB assay) was performed on all patients, and isoniazid treatment was given to those with clinical risk factors for latent TB infection (LTBI). Patients with positive IGRA who had no clinical risk factors for LTBI were randomly assigned to isoniazid treatment or a control group. The development of TB after KT was monitored between June 2010 and November 2013. The primary endpoint was the development of TB.
Of the 784 patients who had no clinical risk factors for LTBI, 445 (57%) gave negative results in the IGRA, 76 (10%) indeterminate results and 263 (33%) positive results. Of the latter, 131 were allocated to isoniazid treatment and 132 to the control group. Three (2%) of the control group developed TB, whereas none of the isoniazid treatment group developed TB (rate difference 1.22 per 100 person-years, P = 0.09). Of the 521 patients with negative or indeterminate IGRA results, 4 [0.8%, 0.43 per 100 person-years (95% CI 0.12-1.09)] developed TB after KT.
IGRA-based isoniazid treatment has a trend towards reducing TB development in KT recipients without clinical risk factors, but careful monitoring of TB development is needed in negative-IGRA KT recipients.
我们在一个结核病负担中等的国家,对肾移植(KT)受者开展了一项基于干扰素-γ释放试验(IGRA)的异烟肼治疗随机试验。
纳入2010年6月至2013年5月期间入住一家KT机构的所有成年患者。对所有患者进行IGRA(T-SPOT.TB检测),并对有潜伏性结核感染(LTBI)临床危险因素的患者给予异烟肼治疗。IGRA结果为阳性且无LTBI临床危险因素的患者被随机分配至异烟肼治疗组或对照组。在2010年6月至2013年11月期间监测KT后结核病的发生情况。主要终点是结核病的发生。
在784例无LTBI临床危险因素的患者中,445例(57%)IGRA结果为阴性,76例(10%)结果不确定,263例(33%)结果为阳性。在后者中,131例被分配至异烟肼治疗组,132例被分配至对照组。对照组中有3例(2%)发生结核病,而异烟肼治疗组中无人发生结核病(率差为每100人年1.22,P = 0.09)。在521例IGRA结果为阴性或不确定的患者中,4例[0.8%,每100人年0.43(95%CI 0.12 - 1.09)]在KT后发生结核病。
基于IGRA的异烟肼治疗在无临床危险因素的KT受者中有降低结核病发生的趋势,但对于IGRA结果为阴性的KT受者,需要仔细监测结核病的发生情况。