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Impact of molecular diagnostic tests on diagnostic and treatment delays in tuberculosis: a systematic review and meta-analysis.
Lee, Jae Hyoung; Garg, Tushar; Lee, Jungsil; McGrath, Sean; Rosman, Lori; Schumacher, Samuel G; Benedetti, Andrea; Qin, Zhi Zhen; Gore, Genevieve; Pai, Madhukar; Sohn, Hojoon.
Affiliation
  • Lee JH; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, USA.
  • Garg T; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, USA.
  • Lee J; London School of Hygiene & Tropical Medicine, London, UK.
  • McGrath S; Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, USA.
  • Rosman L; Welch Medical Library, John Hopkins University School of Medicine, Baltimore, USA.
  • Schumacher SG; Foundation for Innovative New Diagnostics, Geneva, Switzerland.
  • Benedetti A; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada.
  • Qin ZZ; Respiratory Epidemiology & Clinical Research Unit, McGill University Health Centre, Montreal, Canada.
  • Gore G; Stop TB Partnership, Geneva, Switzerland.
  • Pai M; Schulich Library of Physical Sciences, Life Sciences, and Engineering, McGill University, Montreal, Canada.
  • Sohn H; McGill International TB Centre, McGill University, Montreal, Canada.
BMC Infect Dis ; 22(1): 940, 2022 Dec 14.
Article in En | MEDLINE | ID: mdl-36517736
BACKGROUND: Countries with high TB burden have expanded access to molecular diagnostic tests. However, their impact on reducing delays in TB diagnosis and treatment has not been assessed. Our primary aim was to summarize the quantitative evidence on the impact of nucleic acid amplification tests (NAAT) on diagnostic and treatment delays compared to that of the standard of care for drug-sensitive and drug-resistant tuberculosis (DS-TB and DR-TB). METHODS: We searched MEDLINE, EMBASE, Web of Science, and the Global Health databases (from their inception to October 12, 2020) and extracted time delay data for each test. We then analysed the diagnostic and treatment initiation delay separately for DS-TB and DR-TB by comparing smear vs Xpert for DS-TB and culture drug sensitivity testing (DST) vs line probe assay (LPA) for DR-TB. We conducted random effects meta-analyses of differences of the medians to quantify the difference in diagnostic and treatment initiation delay, and we investigated heterogeneity in effect estimates based on the period the test was used in, empiric treatment rate, HIV prevalence, healthcare level, and study design. We also evaluated methodological differences in assessing time delays. RESULTS: A total of 45 studies were included in this review (DS = 26; DR = 20). We found considerable heterogeneity in the definition and reporting of time delays across the studies. For DS-TB, the use of Xpert reduced diagnostic delay by 1.79 days (95% CI - 0.27 to 3.85) and treatment initiation delay by 2.55 days (95% CI 0.54-4.56) in comparison to sputum microscopy. For DR-TB, use of LPAs reduced diagnostic delay by 40.09 days (95% CI 26.82-53.37) and treatment initiation delay by 45.32 days (95% CI 30.27-60.37) in comparison to any culture DST methods. CONCLUSIONS: Our findings indicate that the use of World Health Organization recommended diagnostics for TB reduced delays in diagnosing and initiating TB treatment. Future studies evaluating performance and impact of diagnostics should consider reporting time delay estimates based on the standardized reporting framework.
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Full text: 1 Collection: 01-internacional Health context: 2_ODS3 / 3_ND Database: MEDLINE Main subject: Tuberculosis / Tuberculosis, Pulmonary / Tuberculosis, Multidrug-Resistant / Mycobacterium tuberculosis Type of study: Diagnostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: BMC Infect Dis Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 2_ODS3 / 3_ND Database: MEDLINE Main subject: Tuberculosis / Tuberculosis, Pulmonary / Tuberculosis, Multidrug-Resistant / Mycobacterium tuberculosis Type of study: Diagnostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: BMC Infect Dis Year: 2022 Document type: Article