Background. Active tuberculosis (TB) must be excluded before initiating isoniazid preventive therapy (IPT) in persons infected with human immunodeficiency virus (HIV), but currently used screening strategies have poor sensitivity and specificity and high patient attrition rates. Liquid TB culture is now recommended for the detection of Mycobacterium tuberculosis in individuals suspected of having TB. This study compared the efficacy, effectiveness, and speed of the microscopic observation drug susceptibility (MODS) assay with currently used strategies for TB screening before IPT in HIV-infected persons. Methods. A total of 471 HIV-infected IPT candidates at 3 hospitals in Lima, Peru, were enrolled in a prospective comparison of TB screening strategies, including laboratory, clinical, and radiographic assessments. Results. Of 435 patients who provided 2 sputum samples, M. tuberculosis was detected in 27 (6.2%) by MODS culture, 22 (5.1%) by Lowenstein-Jensen culture, and 7 (1.6%) by smear. Of patients with any positive microbiological test result, a MODS culture was positive in 96% by 14 days and 100% by 21 days. The MODS culture simultaneously detected multidrug-resistant TB in 2 patients. Screening strategies involving combinations of clinical assessment, chest radiograph, and sputum smear were less effective than 2 liquid TB cultures in accurately diagnosing and excluding TB (P < .01). Screening strategies that included nonculture tests had poor sensitivity and specificity. Conclusions. MODS culture identified and reliably excluded cases of pulmonary TB more accurately than other screening strategies, while providing results significantly faster than Lowenstein-Jensen culture. Streamlining of the ruling out of TB through the use of liquid culture-based strategies could help facilitate the massive upscaling of IPT required to reduce HIV and TB morbidity and mortality.
|Number of pages||9|
|Journal||Clinical Infectious Diseases|
|State||Published - 1 Apr 2010|
Bibliographical noteFunding Information:
Financial support. This work was supported by Wellcome Trust Career Development Fellowship 078067/Z/05 (D.A.J.M.), National Institutes of Health/Fogarty Global Research Training grant 3D43 TW006581–04S1 (R.H.G.), and National Institutes of Health/Fogarty International Clinical Research Scholar Awards (K.P.R. and M.F.B.). J.S.F. and D.A.J.M. are grateful for support from the National Institute for Health Research Biomedical Research Centre funding scheme. Potential conflicts of interest. All authors: no conflicts.