• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Lancet. Apr 30, 2011; 377(9776): 1495–1505.
PMCID: PMC3085933

Feasibility, diagnostic accuracy, and effectiveness of decentralised use of the Xpert MTB/RIF test for diagnosis of tuberculosis and multidrug resistance: a multicentre implementation study

Summary

Background

The Xpert MTB/RIF test (Cepheid, Sunnyvale, CA, USA) can detect tuberculosis and its multidrug-resistant form with very high sensitivity and specificity in controlled studies, but no performance data exist from district and subdistrict health facilities in tuberculosis-endemic countries. We aimed to assess operational feasibility, accuracy, and effectiveness of implementation in such settings.

Methods

We assessed adults (≥18 years) with suspected tuberculosis or multidrug-resistant tuberculosis consecutively presenting with cough lasting at least 2 weeks to urban health centres in South Africa, Peru, and India, drug-resistance screening facilities in Azerbaijan and the Philippines, and an emergency room in Uganda. Patients were excluded from the main analyses if their second sputum sample was collected more than 1 week after the first sample, or if no valid reference standard or MTB/RIF test was available. We compared one-off direct MTB/RIF testing in nine microscopy laboratories adjacent to study sites with 2–3 sputum smears and 1–3 cultures, dependent on site, and drug-susceptibility testing. We assessed indicators of robustness including indeterminate rate and between-site performance, and compared time to detection, reporting, and treatment, and patient dropouts for the techniques used.

Findings

We enrolled 6648 participants between Aug 11, 2009, and June 26, 2010. One-off MTB/RIF testing detected 933 (90·3%) of 1033 culture-confirmed cases of tuberculosis, compared with 699 (67·1%) of 1041 for microscopy. MTB/RIF test sensitivity was 76·9% in smear-negative, culture-positive patients (296 of 385 samples), and 99·0% specific (2846 of 2876 non-tuberculosis samples). MTB/RIF test sensitivity for rifampicin resistance was 94·4% (236 of 250) and specificity was 98·3% (796 of 810). Unlike microscopy, MTB/RIF test sensitivity was not significantly lower in patients with HIV co-infection. Median time to detection of tuberculosis for the MTB/RIF test was 0 days (IQR 0–1), compared with 1 day (0–1) for microscopy, 30 days (23–43) for solid culture, and 16 days (13–21) for liquid culture. Median time to detection of resistance was 20 days (10–26) for line-probe assay and 106 days (30–124) for conventional drug-susceptibility testing. Use of the MTB/RIF test reduced median time to treatment for smear-negative tuberculosis from 56 days (39–81) to 5 days (2–8). The indeterminate rate of MTB/RIF testing was 2·4% (126 of 5321 samples) compared with 4·6% (441 of 9690) for cultures.

Interpretation

The MTB/RIF test can effectively be used in low-resource settings to simplify patients' access to early and accurate diagnosis, thereby potentially decreasing morbidity associated with diagnostic delay, dropout and mistreatment.

Funding

Foundation for Innovative New Diagnostics, Bill & Melinda Gates Foundation, European and Developing Countries Clinical Trials Partnership (TA2007.40200.009), Wellcome Trust (085251/B/08/Z), and UK Department for International Development.

Introduction

Two of the three key infectious diseases of man, HIV and malaria, can be diagnosed in primary-care settings with straightforward rapid tests. No such technology has been available to accurately detect tuberculosis and its drug-resistant forms, and this absence has been a major obstacle to improvement of tuberculosis care and reduction of the global burden of disease. Microscopy alone, although inexpensive, misses many patients and detects only those with relatively advanced disease.1–3 Presently, only 28% of expected incident cases of tuberculosis are detected and reported as smear positive.4 Undetected cases of disease increase morbidity, mortality, and disease transmission.5–7 In many countries, epidemic HIV infection has further reduced the sensitivity of microscopy and increased the necessity of rapid diagnosis of tuberculosis. The mortality of untreated or mistreated tuberculosis in people with advanced HIV is high.8–10 Autopsy studies in various countries have shown that 30–60% of people with HIV infection may die with tuberculosis, often undiagnosed, moving the cure-rate target of 85% for tuberculosis out of reach unless available diagnostic technologies can be improved.11,12

Multidrug-resistant tuberculosis is an increasing concern globally and directly threatens disease-control efforts in many countries.13 Only 30 000 of nearly 500 000 new cases of multidrug-resistant tuberculosis every year13 are detected and reported,4 and misdiagnosis causes thousands of deaths, nosocomial and community transmission, and amplification of drug resistance.14–16

In recognition of these issues, substantial efforts are being made to strengthen laboratory capacity to diagnose smear-negative and multidrug-resistant tuberculosis, including increased use of solid and liquid culture, conventional drug-susceptibility testing, and line-probe assays. Unfortunately, these tests require extensive laboratory infrastructure and cannot be done outside of reference facilities.

Recently, a real-time PCR assay for Mycobacterium tuberculosis that simultaneously detects rifampicin resistance was developed on the GeneXpert platform (Cepheid, Sunnyvale, CA, USA), which integrates sample processing and greatly simplifies testing.17,18 This assay, Xpert MTB/RIF, showed excellent performance in a multicentre study19 undertaken in reference laboratories. In the study,19 one-off direct MTB/RIF testing detected 92·2% of cases of pulmonary tuberculosis, including 72·5% of those with smear-negative disease, which was equivalent to that reported for solid culture.

Diagnostic tests often do well in initial studies that are usually done in near-ideal settings in reference laboratories; however, performance is frequently reduced when assays are tested in settings of intended use. In our study, we aimed to establish whether the MTB/RIF test was robust enough to retain high accuracy when used in district and subdistrict health facilities in resource-poor countries, and to measure the operational feasibility and effectiveness of its implementation in such settings.

Methods

Study population

In our multicentre implementation study, we enrolled adults aged 18 years or older with at least 2 weeks of cough who presented consecutively to urban or periurban primary-care health centres in South Africa, Peru, and India, to drug-resistance screening facilities in Azerbaijan and the Philippines, and to an emergency room at a central hospital in Uganda, and provided at least two sputum samples. Patients were excluded from the main analyses if their second sputum sample was collected more than 1 week after the first sample, if no culture was done, or if there was no valid culture, no valid MTB/RIF test result, smear-positive with no positive cultures, only one positive culture with 20 or fewer colonies for solid culture or more than 28 days to positivity for liquid culture, a positive culture during follow-up only, only one a positive culture with missing speciation result, a positive culture with only non-tuberculous mycobacterial growth, or discrepant rifampicin results by conventional drug-susceptibility testing on two samples.

We established the MTB/RIF test in the microscopy area of nine laboratories that were located within the same building at eight sites or a nearby building at one site (in one of two sites in Cape Town, South Africa). We chose study sites to represent diverse populations of patients and laboratory capacities. Sites in South Africa and Uganda served populations with a high prevalence of HIV, centres in Peru and India served populations with low prevalence of HIV and multidrug-resistant tuberculosis, and sites in Azerbaijan and the Philippines served populations with a high prevalence of multidrug-resistant tuberculosis.

The study was endorsed by national tuberculosis programmes of participating countries and approved by nine governing institutional review boards. The requirement to obtain individual informed consent was waived by all institutional review boards.

Procedures

Our study was divided into two phases. In the validation phase, MTB/RIF test results were not reported or used for management of patients. This phase allowed the collection of baseline data and confirmed that the site could accurately undertake the MTB/RIF test. In the implementation phase, MTB/RIF test results informed tuberculosis treatment decisions. Before sites could move to the implementation phase they were required to meet predefined performance targets, which were reviewed and approved by the institutional review boards. Table 1 shows the laboratory procedures used in every country. In both phases, participants provided 2–3 sputum samples as per local routine. One sample underwent smear microscopy and direct MTB/RIF testing, the second underwent smear microscopy, culture, and drug-susceptibility testing. The third sample was only collected at sites that routinely required three microscopy results for management of patients.

Table 1
Laboratory procedures

In South Africa, the routine use of bleach-pretreatment for fluorescent microscopy meant that MTB/RIF testing on the same sputum sample was not possible. Therefore, in South Africa we used a study design with weekly alternation between a baseline group and implementation group. In the baseline group, routine smear microscopy from a bleach-treated pellet was done, which was replaced by the MTB/RIF test (used for management of patients) in the implementation group. In both groups, a second specimen was obtained for smear microscopy from a sodium hydroxide (NaOH)-treated pellet, culture, and drug-susceptibility testing.

The MTB/RIF test was done on raw sputum samples with an automated readout provided to the user as described elsewhere.18 GeneXpert four-module devices were placed on an open bench in the microscopy area. On the basis of biosafety data,17 the MTB/RIF test sample preparation step was done applying the same local biosafety conditions as for the preparation of microscopy smears: a biosafety cabinet was used at five of the nine sites. Temperature logs were placed at each facility to record the operating and reagent storage temperatures. Laboratory staff chosen as MTB/RIF test operators had little experience with laboratory methods other than smear microscopy, had never undertaken molecular testing, and had basic or no computer skills (see webappendix p 1). Masking, which was not necessary in South Africa due to study design, was accomplished at the other sites by having different staff do smear microscopy and MTB/RIF testing.

The reference standard, quality-assured culture and drug-susceptibility testing, was done at reference laboratories located within 1 h of MTB/RIF test sites. Samples undergoing Löwenstein–Jensen or liquid culture (Bactec MGIT; BD Microbiology Systems, Cockeysville, MD, USA) were processed with standard N-acetyl-L-cysteine–NaOH (2%) decontamination. For Ogawa culture, sputum specimens were decontaminated with the modified Petroff method.20 All positive cultures underwent MPT64-based (Capilia tuberculosis assay; Tauns, Numazu, Japan) species confirmation21 and, if positive for M tuberculosis, conventional drug-susceptibility testing with Löwenstein–Jensen proportion or mycobacteria growth indicator tube (MGIT). In South Africa, the line-probe assay MTBDRplus (Hain Lifescience, Nehren, Germany) was done on NaOH-treated pellets for smear-positive sputum and on culture isolates for smear-negative sputum. Conventional drug-susceptibility testing was then used for specimens testing positive for drug-resistance-associated mutations. In Uganda, line-probe assay and, for 10% of culture positive patients (every tenth patient), Löwenstein–Jensen proportion was performed on MGIT isolates (except when only positive on Löwenstein–Jensen). HIV results were obtained from clinical records.

Clinicians categorised participants into two groups: patients who had suspected tuberculosis and presented for case detection and patients with suspected multidrug-resistant tuberculosis who presented for resistance detection (patients who received tuberculosis treatment within the past year or had contact with multidrug-resistant tuberculosis). For analysis, patients with suspected tuberculosis were divided into four categories: smear-positive and culture-positive pulmonary tuberculosis; smear-negative and culture-positive pulmonary tuberculosis; smear-negative, culture-negative and not treated (non-tuberculosis); and smear-negative and culture-negative but treated for tuberculosis on the basis of clinical and radiological findings (clinical tuberculosis). A patient was regarded as having smear-positive tuberculosis on the basis of at least two scanty smears (1–9 bacilli per 100 fields [1000× for light microscopy and 400× for fluorescence microscopy]) or one or more smears of grade 1+ or higher (10–99 bacilli per 100 fields). A culture-positive case was defined as the isolation of M tuberculosis in at least one culture. Patients who were culture-positive (suspected tuberculosis and multidrug-resistant tuberculosis) were categorised as sensitive or resistant to rifampicin.

Statistical analysis

We calculated sensitivity and specificity of the MTB/RIF test for each patient category stratified by HIV and smear microscopy status, and used the results of all microscopy and culture examinations to classify patients into the four groups. To prevent selection bias, patients with suspected multidrug-resistant tuberculosis were only included in the analysis of MTB/RIF test rifampicin-detection endpoints.

We quantitatively assessed operational feasibility of introduction of the MTB/RIF test by examining indicators of robustness such as indeterminate rate, frequency of DNA contamination events, and variation of performance in time and between sites. We used a hands-on and question-based proficiency test and user-appraisal questionnaire to qualitatively establish the minimal training needs and ease of use. The Foundation for Innovative New Diagnostics (FIND; Geneva, Switzerland) study team did the training.

We assessed effectiveness of every method by examining the time to detection of tuberculosis and rifampicin resistance and the time to reporting of results to the clinics. Additionally, we compared the time to treatment initiation from first sputum collection and the dropout rate (patients with confirmed tuberculosis who had not started treatment) between validation and implementation phases.

Within sites we measured association between variables with the Pearson's χ2 test and between sites we used the Cochran-Mantel-Haenszel statistic. We did within-patient analysis with McNemar's test. We did a subgroup analysis for excluded patients. All analyses were done with SAS version 9.2, and p<0·05 was regarded as significant.

Role of the funding source

The FIND cosponsored the study and led study design, training, study coordination and monitoring, data analysis, and writing of the report. The other sponsors of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the report. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication.

Results

From Aug 11, 2009, until June 26, 2010, we enrolled 6648 eligible adults (figure 1, tables 2 and 3). One-off MTB/RIF testing correctly detected tuberculosis in more than 90% of patients with positive cultures, with 99% specificity for non-tuberculosis (table 4). Performance was much the same during validation and implementation phases (webappendix p 2). A one-off MTB/RIF test identified significantly (p<0·0001) more cases of tuberculosis than did 2–3 smear microscopy examinations per patient, which detected 699 of 1041 culture-positive patients (sensitivity of 67·1%) and 3700 of 3718 patients without tuberculosis (specificity of 99·5%). Although HIV co-infection significantly decreased the sensitivity of smear microscopy (p<0·0001), the sensitivity of MTB/RIF was not significantly affected by HIV co-infection status (p=0·0849; table 5). MTB/RIF test sensitivity and specificity were much the same between basic health centres and sites with increased capacity both between countries (p=0·895 and p=0·097, respectively; webappendix p 2), and within countries with more than one site (webappendix p 2).

Figure 1
Study profile
Table 2
Characteristics of patients and study sites
Table 3
HIV statuses in patients with suspected cases of tuberculosis and multidrug-resistant tuberculosis
Table 4
Sensitivity, specificity, and predictive values of a one-off direct MTB/RIF test
Table 5
Sensitivity and specificity of smear microscopy (two to three microscopy examinations as per routine practice) and a one-off direct MTB/RIF test, stratified by HIV status of patients

Sensitivity of MTB/RIF testing for smear-negative tuberculosis varied between countries (p<0·0001). It was lower at sites that used a reference standard of solid and liquid cultures (Azerbaijan, Uganda, and the Philippines) and slightly higher at sites that tested morning sputum samples rather than spot sputum collections (Peru and India).

MTB/RIF testing correctly identified 242 of 250 cases of rifampicin-resistant tuberculosis (sensitivity of 96·8%) and 779 of 810 rifampicin-sensitive cases (specificity of 96·2%). However, because of concern over false-positive results, especially for settings with a low-prevalence of multidrug-resistant disease, we changed the software cutoff defining drug resistance during the study on May 12, 2010. With modified software definitions, our post-hoc analysis showed that sensitivity decreased to 94·4% and specificity increased to 98·3% (table 6). 17 (6·8%) of 250 cases of rifampicin-resistant tuberculosis were sensitive to isoniazid.

Table 6
MTB/RIF test sensitivity and specificity for detection of rifampicin resistance after change to software cutoff

24 (16%) of 153 patients with clinically diagnosed tuberculosis, but negative culture had positive results on MTB/RIF testing. 20 (83%) of these 24 patients had clinical and radiological follow-up, and all 20 improved on tuberculosis treatment. For the 118 (91%) of 129 patients who tested negative on MTB/RIF but were treated for tuberculosis on the basis of a clinical diagnosis and had clinical and radiological follow-up, only 67 (57%) showed improvement (p<0·0001).

Median time to detection of tuberculosis for the MTB/RIF test was 0 days (IQR 0–1), compared with 1 day (0–1) for smear microscopy, 30 days (23–43) for solid culture, and 16 days (13–21) for liquid culture (figure 2). Median time to detection of rifampicin resistance was 1 day (0–1) for the MTB/RIF test, 20 days (10–26) for line-probe assay (done directly from sputum pellet for smear-positive specimens and from culture isolates for smear-negative specimens) and 106 days (30–124) for phenotypic drug-susceptibility testing (figure 2). Although MTB/RIF testing and microscopy were done near the clinics and results were rapidly received by clinicians (median 1 day [IQR 0–2] for MTB/RIF testing and 2 days [2–3] for microscopy), there were significant delays in receiving results from cultures (median 58 days [42–62]), line-probe assays (40 days [27–53]), and conventional drug-susceptibility testing (63 days [38–102]). Some results were lost or unreported (figure 3).

Figure 2
Proportion of tuberculosis cases detected by each method in culture-positive patients
Figure 3
Proportion of results reported to the clinics for each method from date of first sputum sample

Time between sputum collection and treatment initiation was very dependent on the testing method (figure 4). In the baseline group in South Africa and the validation phase at other sites (ie, when MTB/RIF test results were not used to direct therapy), patients with smear-negative, culture-positive tuberculosis started treatment after a median of 56 days (IQR 39–81). Once MTB/RIF test results were used to direct therapy, the median time-to-treatment for smear-negative tuberculosis reduced to 5 days (2–8). Rates of untreated smear-negative, culture-positive tuberculosis reduced from 39·3% (95% CI 32·6–46·6) at baseline to 14·7% (9·9–21·2) after implementation of the MTB/RIF test.

Figure 4
Time to treatment during validation phase (treatment based on conventional methods only) and implementation phase (treatment based on MTB/RIF test and conventional methods) for patients with smear-positive, culture-positive tuberculosis, smear-negative, ...

GeneXpert provides an indeterminate result if unexpected results occur with any of the internal control measures. The MTB/RIF test was indeterminate in 126 (2%) of 5321 samples tested. 112 repeat tests were successful when adequate sputum remained, with the indeterminate rate reduced to less than 1% (14/5321 samples). In 1449 samples that were positive on MTB/RIF testing, 17 (1%) had indeterminate results for rifampicin resistance. These tests were not repeated. By comparison, the contamination rate was 441 (5%) of 9690 cultures, including repeated cultures from re-decontaminated pellets from all countries apart from South Africa and the Philippines.

Operators without previous molecular biology experience or computer skills passed proficiency testing after 1–3 days of training on MTB/RIF tests, including three hands-on runs. A 1 day online training was successfully used at two sites (Peru and Azerbaijan). Monthly variation in MTB/RIF test performance did not differ between sites (psensitivity=0·52 on Cochran-Mantel-Haenszel test stratified by smear status and pspecificity=0·46 on χ2).

In one of the high HIV-prevalence sites, microscopy was introduced at the same time as MTB/RIF testing. Although MTB/RIF sensitivity for culture-positive tuberculosis at this site was much the same as in other centres (85·9%; 116 of 135 cases), the sensitivity of microscopy with one smear per patient was only 17·8% (21 of 118 smears) compared with 46·6% (55 of 118 smears) with a second smear at the reference laboratory. These findings support the laboratory managers' perception, expressed in user appraisal questionnaires, that MTB/RIF test performance might be less dependent on user skills, motivation, or workload than is microscopy.

We did not detect any DNA contamination events during monthly negative control runs, and test specificity was high across sites. The four-module GeneXpert device was used for 1–24 tests a day with only two incidents needing product support (one network-card failure requiring device replacement and one module replacement). At four sites, the recorded operating temperatures exceeded the maximum recommended operating temperature (15–30°C) during more than 10% of runs. Test performance and frequency of indeterminate results did not show seasonal variation in these sites. In one case, the operating temperature exceeded 40°C and an error message appeared as described in the manual. Several sites had daily temperatures higher than the 2–28°C recommended for cartridge storage temperature; cartridges were stored centrally and distributed twice every month. All sites had power cuts, but used uninterruptible power supplies to support the device during short power cuts and one site used an inverter and serial car batteries during a longer power outage.

Discussion

The MTB/RIF test assay was designed specifically for use close to point-of-treatment in endemic disease settings, and is the first of a new generation of diagnostic tests that have the potential to bring highly sensitive nucleic acid amplification testing to peripheral sections of the health system (panel). In our large multicentre study, MTB/RIF testing in subdistrict microscopy facilities by routine staff with minimal training retained the accuracy seen in previous controlled studies that were undertaken in reference centres.18,19,34–36 Previous studies of the MTB/RIF test that assessed either sputum samples or concentrated, decontaminated sputum pellets, have consistently reported test sensitivity of 72–75% in cases of smear-negative tuberculosis and 98–100% in cases of smear-positive tuberculosis.18,19,34–36 One small retrospective study of 28 frozen pellets reported a sensitivity of 57% for cases of smear-negative tuberculosis.35 In our study, a one-off direct MTB/RIF test detected tuberculosis in more than 90% of patients who were culture positive, including nearly 77% of those with negative smears. The robustness of these data suggests that the test can be used in various resource-scarce settings for case detection and for rapid decentralised screening of multidrug-resistant tuberculosis. The ability to rapidly detect smear-negative tuberculosis in peripheral settings, including among patients with HIV, is a breakthrough in tuberculosis care and control.

Panel

Research in context

Systematic review

We searched the PubMed database for studies about the Xpert MTB/RIF test published in English up to March 18, 2011, with the search terms “Xpert” or “GeneXpert” and “tuberculosis”. We did not identify any systematic reviews. We identified five studies reporting on performance of the MTB/RIF test for detection of tuberculosis in respiratory specimens.

Interpretation

All studies that we identified were done in research or referral laboratories and were small,18,34–36 apart from one large multicentre assessment.19 Most included testing of previously collected archived samples. In these studies, the reported sensitivity of the MTB/RIF test for detection of smear-positive tuberculosis (98–100%) and smear-negative tuberculosis (72–75%) were consistent, apart from one small study that documented a sensitivity of 57% for smear-negative tuberculosis in 28 previously frozen sputum pellets. With regard to detection of rifampicin resistance, sensitivity and specificity were very high in all previous studies (99–100% sensitivity and 100% specificity after resolution of discordant cases by genotyping), although numbers of rifampicin-resistant cases were small in all studies apart from multicentre assessment. Our study confirms the sensitivity of the MTB/RIF test for smear-positive and smear-negative tuberculosis, when undertaken in routine microscopy centres, and showed reduced, but good, performance for detection of rifampicin resistance. Furthermore, we suggest the MTB/RIF test can provide a substantially reduced time to detection and treatment for smear-negative tuberculosis.

This is the first study in which MTB/RIF test results have been made available to clinic staff to inform patient management, and hence the first to describe the effect on time to detection and treatment. The short turnaround time resulted in substantially faster initiation of appropriate tuberculosis therapy, particularly for patients with smear-negative disease, and lower dropout rates. Many patients with tuberculosis drop out during the diagnostic process through failing to submit specimens for microscopy when prescribed,37 submitting an initial specimen but not returning,38 or not receiving or acting on positive test results.39–41 Rapid testing, even if less sensitive than slower methods, can result in more patients being correctly treated. Overall, patient dropout with one-off MTB/RIF testing could possibly be reduced even further in routine conditions, as our analysis excluded 640 (9%) of 7288 enrolled patients who did not provide a second sample (figure 1). Although treatment decisions for multidrug-resistant tuberculosis were not informed by MTB/RIF test results, delays in result reporting for rapid, but centralised drug-susceptibility testing (line-probe assay and MGIT drug-susceptibility testing) were substantially shortened by decentralised MTB/RIF testing, and would probably translate into reduced time-to-appropriate-treatment.

Although the sensitivity and specificity of MTB/RIF test for detection of rifampicin resistance in this study was high (94·4% sensitivity and 98·3% specificity), accuracy was higher in previous publications (99–100% sensitivity and 100% specificity after discordant resolution by genotyping).18,19,34–36 Assay development partners are working to further improve MTB/RIF test accuracy of detection of multidrug-resistant tuberculosis. The low positive-predictive value of MTB/RIF for rifampicin resistance detection that we noted in patients with a low pretest probability of multidrug-resistant tuberculosis might justify the need for confirmatory testing with conventional methods in such settings.

Several issues might restrict the applicability of the MTB/RIF test at small health centres. The device requires stable electricity supply, although some centres successfully tested battery operation. Device deployment above 30°C is presently not recommended by the manufacturer and cartridges are confirmed as stable at 2–28°C (efforts are ongoing to increase the operating and storage temperatures). There were few device breakdowns in this study as the devices used were new, and there are no data for their extended use in dusty and humid conditions. The GeneXpert device needs calibration yearly, which requires either access to an MTB/RIF test distributor or internal capacity to replace modules as per manufacturer instructions.

In the study, MTB/RIF test cartridges were handled with the same level of biosafety as microscopy. As the MTB/RIF tuberculosis assay was designed to keep biohazards to a minimum, the risk should be substantially lower than that noted in microscopy. As published elsewhere,17 the only specimen processing required is the addition of a sample reagent that is bactericidal and results in a 107 reduction in viable mycobacteria in the first 15 min. Additionally, unlike smear microscopy, the manual pipetting steps and the automated portion of the assay do not generate viable mycobacterial aerosols.17 Together, these results suggest that the MTB/RIF test can be done without special biosafety precautions.

Our study findings have several limitations. The use of different study designs and diagnostic algorithms across sites made a direct comparison of findings challenging. Our study did not allow us to determine the effect of rapid and early detection on the number of patients treated and on treatment outcomes, as longterm follow-up was not undertaken and as the parallel use of culture, not otherwise routinely available, may have affected physicians' choices. Additionally, the study did not include any testing of close contacts to measure effect on transmission. Participating sites were urban or periurban and supply chain management, reagent storage, and calibration are likely to be more problematic in rural areas.

Overall, our findings suggest that decentralised MTB/RIF test implementation is feasible and could lead to an improvement in tuberculosis care and control. Any improvement will require increased detection of tuberculosis and multidrug-resistant-tuberculosis to coincide with scale-up of first-line, and more importantly, second-line treatment.42 Whether early and appropriate treatment after MTB/RIF testing can reduce tuberculosis-associated morbidity and mortality, and its effect on transmission, needs to be established.

Acknowledgments

We thank the study teams for their efforts to complete data collection in time for the WHO expert review meeting, the National tuberculosis Control Programmes and Laboratory Services and Médecins Sans Frontieres for their support in the planning and conduct of the study, and Sean O'Brien from Duke University (Durham NC, USA) for his support during data analysis.

Contributors

CCB and MPN designed the study. CG, CCB, PN, FC, MDP, and MPN analysed the final data and developed the first manuscript draft. All authors contributed to data collection, interpretation of data, and revision of the article.

Conflicts of interest

CCB, PN, CG, HAlb, and MDP are employed by the Foundation for Innovative New Diagnostics (FIND, Geneva, Switzerland), a non-profit organisation that collaborates with industry partners, including Cepheid (Sunnyvale, CA, USA), on the development, assessment, and demonstration of new diagnostic tests. HAle was a consultant for FIND. DA has been a consultant to Cepheid and received royalties personally; DA and RB's institution received royalties under a licensing agreement between University of Medicine and Dentistry of New Jersey (Newark, NJ, USA) and Cepheid. DA's royalties generated by the Xpert assay have been voluntarily (but irrevocably) capped at US$5000 per year (personal income) and $50 000 per year (laboratory income) to mitigate potential conflicts of interest. No commercial partner was involved in the study.

Web Extra Material

Supplementary webappendix:

References

1. Bruchfeld J, Aderaye G, Palme IB, Bjorvatn B, Kallenius G, Lindquist L. Sputum concentration improves diagnosis of tuberculosis in a setting with a high prevalence of HIV. Trans R Soc Trop Med Hyg. 2000;94:677–680. [PubMed]
2. Perkins MD, Cunningham J. Facing the crisis: improving the diagnosis of tuberculosis in the HIV era. J Infect Dis. 2007;196:S15–S27. [PubMed]
3. Steingart KR, Ramsay A, Pai M. Optimizing sputum smear microscopy for the diagnosis of pulmonary tuberculosis. Expert Rev Anti Infect Ther. 2007;5:327–331. [PubMed]
4. World Health Organization Global tuberculosis control. 2010. http://whqlibdoc.who.int/publications/2010/9789241564069_eng.pdf (accessed March 18, 2011).
5. Behr MA, Warren SA, Salamon H. Transmission of Mycobacterium tuberculosis from patients smear-negative for acid-fast bacilli. Lancet. 1999;353:444–449. [PubMed]
6. Havlir DV, Barnes PF. Tuberculosis in patients with human immunodeficiency virus infection. N Engl J Med. 1999;340:367–373. [PubMed]
7. Millen SJ, Uys PW, Hargrove J, van Helden PD, Williams BG. The effect of diagnostic delays on the drop-out rate and the total delay to diagnosis of tuberculosis. PLoS One. 2008;3:e1933. [PMC free article] [PubMed]
8. Garin B, Glaziou P, Kassa-Kelembho E, Yassibanda S, Mbelesso P, Morvan J. High mortality rates among patients with tuberculosis in Bangui, Central African Republic. Lancet. 1997;350:1298. [PubMed]
9. Harries AD, Nyangulu DS, Kang'ombe C. Treatment outcome of an unselected cohort of tuberculosis patients in relation to human immunodeficiency virus serostatus in Zomba Hospital, Malawi. Trans R Soc Trop Med Hyg. 1998;92:343–347. [PubMed]
10. Mukadi YD, Maher D, Harries A. Tuberculosis case fatality rates in high HIV prevalence populations in sub-Saharan Africa. AIDS. 2001;15:143–152. [PubMed]
11. Pronyk PM, Kahn K, Hargreaves JR. Undiagnosed pulmonary tuberculosis deaths in rural South Africa. Int J Tuberc Lung Dis. 2004;8:796–799. [PubMed]
12. Lanjewar DN, Duggal R. Pulmonary pathology in patients with AIDS: an autopsy study from Mumbai. HIV Med. 2001;2:266–271. [PubMed]
13. World Health Organization Multidrug and extensively drug-resistant TB (M/XDR-TB): 2010 global report on surveillance and response. http://whqlibdoc.who.int/publications/2010/9789241599191_eng.pdf (accessed Feb 15, 2011).
14. Farmer P, Bayona J, Becerra M. The dilemma of MDR-TB in the global era. Int J Tuberc Lung Dis. 1998;2:869–876. [PubMed]
15. Fischl MA, Daikos GL, Uttamchandani RB. Clinical presentation and outcome of patients with HIV infection and tuberculosis caused by multiple-drug-resistant bacilli. Ann Intern Med. 1992;117:184–190. [PubMed]
16. Van Rie A, Enarson D. XDR tuberculosis: an indicator of public-health negligence. Lancet. 2006;368:1554–1556. [PubMed]
17. Banada PP, Sivasubramani SK, Blakemore R. Containment of bioaerosol infection risk by the Xpert MTB/RIF assay and its applicability to point-of-care settings. J Clin Microbiol. 2010;48:3551–3557. [PMC free article] [PubMed]
18. Helb D, Jones M, Story E. Rapid detection of Mycobacterium tuberculosis and rifampin resistance by use of on-demand, near-patient technology. J Clin Microbiol. 2010;48:229–237. [PMC free article] [PubMed]
19. Boehme CC, Nabeta P, Hillemann D. Rapid molecular detection of tuberculosis and rifampin resistance. N Engl J Med. 2010;363:1005–1015. [PMC free article] [PubMed]
20. World Health Organization Services in tuberculosis control part III: Culture. http://whqlibdoc.who.int/hq/1998/WHO_TB_98.258_(part3).pdf (accessed April 6, 2011).
21. Hillemann D, Rüsch-Gerdes S, Richter E. Application of the Capilia TB assay for culture confirmation of Mycobacterium tuberculosis complex isolates. Int J Tuberc Lung Dis. 2005;9:1409–1411. [PubMed]
22. World Health Organization Tuberculosis country profiles. http://www.who.int/tb/country/data/profiles/en/index.html (accessed March 21, 2011).
23. Médecins Sans Frontières. Western Cape Department of Health. City of Cape Town Department of Health. City of Cape Town Department of Health and University of Cape Town. Centre for Infectious Disease Epidemiology and Research . Providing HIV/TB care at the primary health care level. Khayelitsha annual activity report 2008–2009. Médecins Sans Frontières; Sea Point, South Africa: 2010.
24. English R, Information Management Office . Boland/Overberg region annual health status report 2007/2008. Boland/Overberg regional office; Worcester, UK: 2008.
25. Central TB Division. Directorate General of Health Services Ministry of Health and Family Welfare Revised national tuberculosis control programme, performance report, India. 2010. http://www.tbcindia.org/pdfs/Perf%203Q%202010.pdf (accessed March 21, 2011).
26. Tropical Disease Foundation. Department of Health Republic of the Philippines, 2007 Nationwide Tuberculosis Prevalence Survey.
27. Asencios L, Quispe N, Mendoza-Ticona A. Vigilancia nacional de la resistencia a medicamentos antituberculosos, Peru 2005–2006. Rev Peru Med Exp Salud Publica. 2009;26:278–287.
28. Wright A, Zignol M, Van Deun A. Epidemiology of antituberculosis drug resistance 2002–07: an updated analysis of the global project on anti-tuberculosis drug resistance surveillance. Lancet. 2009;373:1861–1873. [PubMed]
29. Médecins Sans Frontières . Scaling up diagnosis and treatment of drug-resistant tuberculosis in Khayelitsha, South Africa. An integrated, community-based approach. Médecins Sans Frontières; Cape Town, South Africa: 2011.
30. Lukoye D, Cobelens FGJ, Ezati N. Rates of anti-tuberculosis drug resistance in Kampala-Uganda are low and not associated with HIV infection. PLoS One. 2011;6:e16130. [PMC free article] [PubMed]
31. Philippine Nationwide Tuberculosis Drug Resistance Survey Team Nationwide drug resistance survey of tuberculosis in the Philippines. Int J Tuberc Lung Dis. 2009;13:500–507. [PubMed]
32. Mendoza-Ticona A, Iglesias-Quilca D. Tuberculosis en pacientes con VIH/SIDA. Acta Med Per. 2008;25:247–254.
33. Stop TB Department World Health Organization European Region. Accelerating the implementation of collaborative TB/HIV activities in the WHO European Region; Vienna, Austria; July 16–17, 2010.
34. Marlowe EM, Novak Weekley SM, Cumpio J. Evaluation of the cepheid Xpert MTB/RIF assay for the direct detection of Mycobacterium tuberculosis complex from respiratory specimens. J Clin Microbiol. 2011 published online Feb 2. [PMC free article] [PubMed]
35. Armand S, Vanhuls P, Delcroix G, Courcol R, Lemaître N. Comparison of the Xpert MTB/RIF test with an IS6110-TagMan real-time PCR assay for direct detection of Mycobacterium tuberculosis in respiratory and nonrespiratory specimens. J Clin Microbiol. 2011 published online March 16. [PMC free article] [PubMed]
36. Moure R, Muñoz L, Torres M, Santin M, Martin R, Alcaide F. Rapid detection of Mycobacterium tuberculosis complex and rifampin resistance in smear-negative clinical samples by use of an integrated real-time PCR method. J Clin Microbiol. 2011;49:1137–1139. [PMC free article] [PubMed]
37. Long Q, Li Y, Wang Y. Barriers to accessing TB diagnosis for rural-to-urban migrants with chronic cough in Chongqing, China: a mixed methods study. BMC Health Serv Res. 2008;8:202. [PMC free article] [PubMed]
38. Khan MS, Khan S, Godfrey-Faussett P. Default during TB diagnosis: quantifying the problem. Trop Med Int Health. 2009;14:1437–1441. [PubMed]
39. Rao NA, Anwer T, Saleem M. Magnitude of initial default in pulmonary tuberculosis. J Pak Med Assoc. 2009;59:223–225. [PubMed]
40. Botha E, Den Boon S, Verver S. Initial default from tuberculosis treatment: how often does it happen and what are the reasons? Int J Tuberc Lung Dis. 2008;12:820–823. [PubMed]
41. Squire SB, Belaye AK, Kashoti A. ‘Lost’ smear-positive pulmonary tuberculosis cases: where are they and why did we lose them? Int J Tuberc Lung Dis. 2005;9:25–31. [PubMed]
42. Stop TB Department WHO Roadmap for rolling out Xpert MTB/RIF for rapid diagnosis of TB and MDR-TB. http://www.who.int/tb/laboratory/roadmap_xpert_mtb-rif.pdf (accessed Feb 15, 2011).

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...