QMAC-DST for Rapid Detection of Drug Resistance in Pulmonary Tuberculosis Patients: A Multicenter Pre–Post Comparative Study

Author:

Kwak Nakwon12ORCID,Lee Sangyeop3,Kim Suyeoun3,Song Eunbee3ORCID,Yim Jae-Joon12,Shim Tae Sun4,Jeon Doosoo56,Jhun Byung Woo7ORCID,Seok Kwang-Hyuk8ORCID,Kim Saerom9,Kwon Sunghoon3,Mok Jeongha6910

Affiliation:

1. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University Hospital, Seoul 03080, Republic of Korea

2. Department of Internal Medicine, Seoul National University College of Medicine, Seoul 03080, Republic of Korea

3. QuantaMatrix Inc., 131 Gasan digital 1-ro, Geumcheon-gu, Seoul 08506, Republic of Korea

4. Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea

5. Department of Internal Medicine, Pusan National University Yangsan Hospital, Yangsan 50612, Republic of Korea

6. Department of Internal Medicine, Pusan National University School of Medicine, Busan 49241, Republic of Korea

7. Division of Pulmonary and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Republic of Korea

8. Department of Laboratory Medicine, The Korean Institute of Tuberculosis, Cheongju 28158, Republic of Korea

9. Department of Internal Medicine, Pusan National University Hospital, 179 Gudeok-ro, Seo-gu, Busan 49241, Republic of Korea

10. Biomedical Research Institute, Pusan National University Hospital, Busan 49241, Republic of Korea

Abstract

Background/Objectives: This study explores the impact of QMAC-DST, a rapid, fully automated phenotypic drug susceptibility test (pDST), on the treatment of tuberculosis (TB) patients. Methods: This pre–post comparative study, respectively, included pulmonary TB patients who began TB treatment between 1 December 2020 and 31 October 2021 (pre-period; pDST using the Löwenstein–Jensen (LJ) DST (M-kit DST)) and between 1 November 2021 and 30 September 2022 (post-period; pDST using the QMAC-DST) in five university-affiliated tertiary care hospitals in South Korea. We compared the turnaround times (TATs) of pDSTs and the time to appropriate treatment for patients whose anti-TB drugs were changed based on these tests between the groups. All patients were permitted to use molecular DSTs (mDSTs). Results: A total of 182 patients (135 in the M-kit DST group and 47 in the QMAC-DST group) were included. The median TAT was 36 days for M-kit DST (interquartile range (IQR), 30–39) and 12 days for QMAC-DST (IQR, 9–15), with the latter being significantly shorter (p < 0.001). Of the total patients, 10 (5.5%) changed their anti-TB drugs based on the mDST or pDST results after initiating TB treatment (8 in the M-kit DST group and 2 in the QMAC-DST group). In the M-kit DST group, three (37.5%) patients changed anti-TB drugs based on the pDST results. In the QMAC-DST group, all changes were due to mDST results; therefore, calculating the time to appropriate treatment for patients whose anti-TB drugs were changed based on pDST results was not feasible. In the QMAC-DST group, 46.8% of patients underwent the first-line line probe assay compared to 100.0% in the M-kit DST group (p < 0.001), indicating that rapid QMAC-DST results provide quicker assurance of the ongoing treatment by confirming susceptibility to the current anti-TB drugs. Conclusions: QMAC-DST delivers pDST results more rapidly than LJ-DST, ensuring faster confirmation for the current treatment regimen.

Funder

Korea Health Industry Development Institute

Publisher

MDPI AG

Reference28 articles.

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