Mobile Digital Fluorescence Microscopy for Diagnosis of Tuberculosis

Author:

Tapley Asa1,Switz Neil2,Reber Clay2,Davis J. Lucian345,Miller Cecily3,Matovu John Baptist67,Worodria William67,Huang Laurence345,Fletcher Daniel A.2,Cattamanchi Adithya345

Affiliation:

1. School of Medicine, University of California, San Francisco, San Francisco, California, USA

2. Bioengineering Department and Biophysics Program, University of California, Berkeley, Berkeley, California, USA

3. Division of Pulmonary & Critical Care Medicine, Department of Medicine, San Francisco General Hospital, University of California, San Francisco, San Francisco, California, USA

4. Curry International Tuberculosis Center, Department of Medicine, San Francisco General Hospital, University of California, San Francisco, San Francisco, California, USA

5. Makerere University-University of California, San Francisco, Research Collaboration, Kampala, Uganda

6. Makerere University School of Medicine, Kampala, Uganda

7. Uganda Ministry of Health, Kampala, Uganda

Abstract

ABSTRACT Access to sputum smear microscopy in high-tuberculosis (TB)-burden regions is limited by a scarcity of microscopes and experienced technicians. We evaluated the accuracy of CellScope, a novel digital fluorescence microscope that may expand access to microscopy. The study utilized smear microscopy slides prepared from sputum specimens submitted by consecutive adults with ≥2 weeks of cough who were admitted to Mulago Hospital (Kampala, Uganda). Conventional light-emitting diode (LED) fluorescence microscopy (FM) and mycobacterial culture were performed by experienced technicians. Two U.S.-based postgraduate researchers without prior microscopy experience restained, imaged, and interpreted the slides using CellScope. We assessed whether sensitivity and specificity of CellScope-based LED FM was noninferior to conventional LED FM by using a preselected margin of inferiority of 15%. Of 525 patients included, 72% were HIV seropositive and 39% had culture-confirmed TB. The proportions of positive results were similar with CellScope and conventional LED FM (34% versus 32%, respectively; P = 0.32), and agreement was substantial. CellScope accuracy was within the noninferiority margin for both sensitivity (63% versus 70%; difference, −7%; 95% confidence interval [CI], −13% to −1%) and specificity (85% versus 92%; difference, −7%; 95% CI, −12% to −3%). A subanalysis of 43 slides evaluated by each CellScope reader found substantial interreader reliability (custom-weighted kappa, 0.65) and variable intrareader reliability (custom-weighted kappa, 0.11 versus 0.48). CellScope offers promise for expanding microscopy services. Future studies should evaluate the device when operated by health workers in low-resource settings, the feasibility of image transmission and analysis by experienced microscopists, and the accuracy of automated image analysis algorithms.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference37 articles.

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