DST/NRF Centre of Excellence for Biomedical Tuberculosis Research, SA MRC Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Division of Infectious Diseases, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 02215, USA.
Sci Rep. 2018 Feb 16;8(1):3206. doi: 10.1038/s41598-018-21458-y.
The scale-up of rapid drug resistance testing for TB is a global priority. MTBDRplus is a WHO-endorsed multidrug-resistant (MDR)-TB PCR assay with suboptimal sensitivities and high indeterminate rates on smear-negative specimens. We hypothesised that widespread use of incorrect thermocycler ramp rate (speed of temperature change between cycles) impacts performance. A global sample of 72 laboratories was surveyed. We tested 107 sputa from Xpert MTB/RIF-positive patients and, separately, dilution series of bacilli, both at the manufacturer-recommended ramp rate (2.2 °C/s) and the most frequently reported incorrect ramp rate (4.0 °C/s). Mycobacterium tuberculosis-complex DNA (TUB-band)-detection, indeterminate results, accuracy, and inter-reader variability (dilution series only) were compared. 32 respondents did a median (IQR) of 41 (20-150) assays monthly. 78% used an incorrect ramp rate. On smear-negative sputa, 2.2 °C/s vs. 4.0 °C/s improved TUB-band positivity (42/55 vs. 32/55; p = 0.042) and indeterminate rates (1/42 vs. 5/32; p = 0.039). The actionable results (not TUB-negative or indeterminate; 41/55 vs. 28/55) hence improved by 21% (95% CI: 9-35%). Widespread use of incorrect ramp rate contributes to suboptimal MTBDRplus performance on smear-negative specimens and hence limits clinical utility. The number of diagnoses (and thus the number of smear-negative patients in whom DST is possible) will improve substantially after ramp rate correction.
快速耐药结核检测的推广是全球的重点。MTBDRplus 是世界卫生组织(WHO)认可的一种多耐药(MDR)-TB PCR 检测方法,其对涂片阴性标本的敏感性不足,不确定率较高。我们假设广泛使用不正确的热循环仪 ramp 率(循环之间的温度变化速度)会影响其性能。对来自全球 72 个实验室的样本进行了调查。我们在制造商推荐的 ramp 率(2.2°C/s)和最常报道的不正确 ramp 率(4.0°C/s)下,分别对 Xpert MTB/RIF 阳性患者的 107 份痰液样本和杆菌稀释系列进行了检测。比较了结核分枝杆菌复合体 DNA(TUB 带)检测、不确定结果、准确性和读者间的可变性(仅在稀释系列中)。32 名受访者每月中位数(IQR)完成 41(20-150)次检测。78%的人使用不正确的 ramp 率。在涂片阴性的痰液样本中,2.2°C/s 与 4.0°C/s 相比,TUB 带阳性率(42/55 与 32/55;p=0.042)和不确定率(1/42 与 5/32;p=0.039)均有所提高。因此,可采取行动的结果(非 TUB 阴性或不确定;41/55 与 28/55)提高了 21%(95%CI:9-35%)。广泛使用不正确的 ramp 率导致 MTBDRplus 在涂片阴性标本上的性能不佳,从而限制了其临床应用。在纠正 ramp 率后,诊断数量(以及可以进行 DST 的涂片阴性患者数量)将大幅增加。