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Feasibility and operational performance of tuberculosis detection by loop-mediated isothermal amplification platform in decentralized settings: Results from a multicenter study

  • Christen M. Gray
  • , Achilles Katamba
  • , Pratibha Narang
  • , Jorge Giraldo
  • , Carlos Zamudio
  • , Moses Joloba
  • , Rahul Narang
  • , C. N. Paramasivan
  • , Doris Hillemann
  • , Pamela Nabeta
  • , Danielle Amisano
  • , David Alland
  • , Frank Cobelens
  • , Catharina C. Boehme
  • Foundation for Innovative New Diagnostics (FIND)
  • Makerere University College of Health Sciences
  • Mahatma Gandhi Institute of Medical Sciences
  • Universidad Peruana Cayetano Heredia, Instituto de Medicina Tropical Alexander von Humboldt
  • National TB Reference Laboratory
  • FIND
  • Research Center Borstel
  • University of Medicine and Dentistry of New Jersey
  • Academic Medical Center
  • KNCV Tuberculosis Foundation

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

50 Citas (Scopus)

Resumen

Currently available nucleic acid amplification platforms for tuberculosis (TB) detection are not designed to be simple or inexpensive enough to implement in decentralized settings in countries with a high burden of disease. The loop-mediated isothermal amplification platform (LAMP) may change this. We conducted a study in adults with symptoms suggestive of TB in India, Uganda, and Peru to establish the feasibility of using TB-LAMP (Eiken Chemical Co.) in microscopy laboratories compared with using smear microscopy against a reference standard of solid and liquid cultures. Operational characteristics were evaluated as well. A total of 1,777 participants met the eligibility criteria and were included for analysis. Overall, TB-LAMP sensitivities among culture-positive samples were 97.2% (243/250; 95% confidence interval [CI], 94.3% to 98.2%) and 62.0% (88/142; 95% CI, 53.5% to 70.0%) for smear-positive and smear-negative TB, respectively, but varied widely by country and operator. Specificities ranged from 94.5% (446/472; 95% CI, 92.0% to 96.4%) to 98.0% (350/357; 95% CI, 96.0% to 99.2%) by country. A root cause analysis identified high temperatures, high humidity, and/or low reaction volumes as possible causes for false-positive results, as they may result in nonspecific amplification. The study was repeated in India with training focused on vulnerable steps and an updated protocol; 580 participants were included for analysis. Specificity in the repeat trial was 96.6% (515/533; 95% CI, 94.7% to 97.9%). To achieve acceptable performance of LAMP at the microscopy center level, significant training and infrastructure requirements are necessary.

Idioma originalInglés
Páginas (desde-hasta)1984-1991
Número de páginas8
PublicaciónJournal of Clinical Microbiology
Volumen54
N.º8
DOI
EstadoPublicada - ago. 2016

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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