Edathodu Jameela, Varghese Bright, Alrajhi Abdulrahman A, Shoukri Mohammed, Nazmi Ahmad, Elgamal Hazem, Aleid Hassan, Alrabiah Fahad, Ashraff Attia, Mahmoud Ihab, Al-Hajoj Sahal
Department of Medicine, King Faisal Specialist Hospital and Research Centre (KFSHRC), Riyadh, Saudi Arabia.
Department of Infection and Immunity, KFSHRC, Riyadh, Saudi Arabia.
Transpl Infect Dis. 2017 Apr;19(2). doi: 10.1111/tid.12675. Epub 2017 Mar 16.
Latent tuberculosis (TB) infection (LTBI) is screened by using clinical assessment, tuberculin skin test (TST), chest radiography, and recently by interferon-gamma release assays (IGRA). The objective of this study was to evaluate the diagnostic potential of QuantiFERON -TB Gold In-Tube test (QFT) for diagnosing LTBI in patients planned for kidney transplantation.
All adult patients with end-stage renal disease, evaluated for kidney transplantation in a referral center from August 2008 till May 2013, were enrolled, after consenting in a prospective, observational, non-interventional study. LTBI diagnosis was conducted by TST, chest x-ray, and clinical assessment, followed by IGRA by QFT.
Overall, 278 patients were enrolled and kidney transplantation was performed in 173 patients. Contributed follow-up was 836.5 patient-years, and TB-free transplant duration was 478.5 patient-years. By standard methods, LTBI was diagnosed in 14 patients. Peri-transplant chemoprophylaxis was given to 53 patients, which included recipients of organs from all deceased donors and living donors with LTBI. QFT was positive in 70 patients, negative in 200 patients, and indeterminate in 8 patients. The agreement between LTBI diagnosis using standard methods and IGRA by QFT was poor (kappa: 0.089+0.046, P-value=.017). Twenty-seven of the QFT-positive patients were transplanted and only one was given isoniazid preventive therapy. None of the transplant recipients developed TB after a median follow-up of 25 months (range 2-58 months, mean 27 months).
The agreement of the QFT with standard diagnosis of LTBI in kidney transplant recipients was poor.
潜伏性结核感染(LTBI)通过临床评估、结核菌素皮肤试验(TST)、胸部X线摄影以及最近的干扰素-γ释放试验(IGRA)进行筛查。本研究的目的是评估全血γ-干扰素释放试验(QFT)对计划进行肾移植患者LTBI的诊断潜力。
2008年8月至2013年5月在一家转诊中心接受肾移植评估的所有成年终末期肾病患者,在同意参加一项前瞻性、观察性、非干预性研究后被纳入。通过TST、胸部X线和临床评估进行LTBI诊断,随后通过QFT进行IGRA检测。
总体而言,共纳入278例患者,其中173例患者接受了肾移植。累计随访时间为836.5患者年,无结核移植持续时间为478.5患者年。通过标准方法诊断出14例LTBI患者。53例患者接受了移植围手术期化学预防,其中包括所有LTBI死亡供体和活体供体器官的接受者。QFT检测结果为阳性的有70例患者,阴性的有200例患者,不确定的有8例患者。使用标准方法诊断LTBI与QFT进行IGRA检测之间的一致性较差(kappa值:0.089±0.046,P值=0.017)。QFT检测阳性的27例患者接受了移植,只有1例接受了异烟肼预防性治疗。中位随访25个月(范围2 - 58个月,平均27个月)后,没有移植受者发生结核病。
QFT与肾移植受者LTBI标准诊断的一致性较差。