Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Department of Biostatistics, Frontier Science Foundation, Brookline, MA, USA.
BMC Infect Dis. 2021 Feb 24;21(1):205. doi: 10.1186/s12879-021-05884-4.
Drug susceptibility testing (DST) patterns of Mycobacterium tuberculosis (MTB) from patients with rifampicin-resistant tuberculosis (RR-TB) or multidrug-resistant TB (MDR-TB; or resistant to rifampicin and isoniazid (INH)), are important to guide preventive therapy for their household contacts (HHCs).
As part of a feasibility study done in preparation for an MDR-TB preventive therapy trial in HHCs, smear, Xpert MTB/RIF, Hain MTBDRplus, culture and DST results of index MDR-TB patients were obtained from routine TB programs. A sputum sample was collected at study entry and evaluated by the same tests. Not all tests were performed on all specimens due to variations in test availability.
Three hundred eight adults with reported RR/MDR-TB were enrolled from 16 participating sites in 8 countries. Their median age was 36 years, and 36% were HIV-infected. Routine testing on all 308 were confirmed as having RR-TB, but only 75% were documented as having MDR-TB. The majority of those not classified as having MDR-TB were because only rifampicin resistance was tested. At study entry (median 59 days after MDR-TB treatment initiation), 280 participants (91%) were able to produce sputum for the study, of whom 147 (53%) still had detectable MTB. All but 2 of these 147 had rifampicin DST done, with resistance detected in 89%. Almost half (47%) of the 147 specimens had INH DST done, with 83% resistance. Therefore, 20% of the 280 study specimens had MDR-TB confirmed. Overall, DST for second-line drugs were available in only 35% of the 308 routine specimens and 15% of 280 study specimens.
RR-TB was detected in all routine specimens but only 75% had documented MDR-TB, illustrating the need for expanded DST beyond Xpert MTB/RIF to target preventive therapy for HHC.
从耐利福平肺结核(RR-TB)或耐多药肺结核(MDR-TB;或耐利福平加异烟肼(INH))患者中获得结核分枝杆菌(MTB)的药物敏感性测试(DST)模式对于指导其家庭接触者(HHC)的预防性治疗非常重要。
作为在 HHC 中进行 MDR-TB 预防性治疗试验的可行性研究的一部分,从常规结核病规划中获得了索引 MDR-TB 患者的涂片、Xpert MTB/RIF、Hain MTBDRplus、培养和 DST 结果。在研究入组时采集了一份痰标本,并通过相同的测试进行了评估。并非所有测试都在所有标本上进行,因为测试可用性存在差异。
从 8 个国家的 16 个参与点招募了 308 名报告有 RR/MDR-TB 的成年人。他们的中位年龄为 36 岁,36%感染了 HIV。对所有 308 例患者进行常规检测均证实患有 RR-TB,但仅 75%被记录为患有 MDR-TB。大多数未被归类为患有 MDR-TB 的患者是因为仅检测到利福平耐药性。在研究入组时(MDR-TB 治疗开始后中位数 59 天),280 名参与者(91%)能够产生研究用痰,其中 147 名(53%)仍可检测到 MTB。这些 147 名参与者中除 2 名外,均进行了利福平 DST 检测,其中 89%检测到耐药性。几乎一半(47%)的 147 个标本进行了 INH DST 检测,其中 83%耐药。因此,280 个研究标本中有 20%确认患有 MDR-TB。总体而言,308 例常规标本中只有 35%和 280 例研究标本中有 15%可获得二线药物 DST。
所有常规标本中均检测到 RR-TB,但仅有 75%记录为 MDR-TB,这表明需要进行扩展的 DST,超出 Xpert MTB/RIF 范围,以针对 HHC 进行预防性治疗。