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Xpert MTB/RIF test for detection of pulmonary tuberculosis
and r ifampicin resistance (Protocol)
Sohn H, Pai M, Dendukuri N , Kloda LA, Boehme CC, Steingart KR
This is a reprint of a Cochrane protocol, prepared and maintained by The Cochrane Collaboration and published in The Cochrane
Library 2012, Issue 1
http://www.thecochranelibrar y.com
Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
T A B L E O F C O N T E N T S
1HEADER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1ABSTRACT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2BACKGROUND . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
3OBJECTIVES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4METHODS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
7ACKNOWLEDGEMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
7REFERENCES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
10APPENDICES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
21HISTORY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
21CONTRIBUTIONS OF AUTHORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
21DECLARATIONS OF INTEREST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
iXpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
[Diagnostic Test Accuracy Protocol]
Xpert MTB/RIF test for detection of pulmonary tuberculosis
and rifampicin resistance
Hojoon Sohn
2
, Madhukar Pai
3
, Nandini Dendukuri
4
, Lorie A Kloda
5
, Catharina C Boehme
6
, Karen R Steingart
1
1
Department of Health Services, University of Washington, School of Public Health, Seattle, Washington, USA.
2
Department of
Epidemiology & Biostatistics, McGill University, Montreal, Canada.
3
Dept of Epidemiology and Biostatistics, McGill University,
Montreal, Canada.
4
Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Canada.
5
Life
Sciences Library, McGill University, Montreal, Canada.
6
FIND, Geneva, Switzerland
Contact address: Karen R Steingart, Department of Health Ser vices, University of Washington, S chool of Public Health, Seattle,
Washington, 98195-7230, USA.
karenst@uw.edu.
Editorial group: Cochrane Infectious Diseases Group.
Publication status and date: New, published in Issue 1, 2012.
Citation: Sohn H, Pai M, Dendukuri N, Kloda LA, Boehme CC, Steingart KR. Xpert MTB/RIF test for detection of pul-
monary tuberculosis and rifampicin resistance. Cochrane Database of Systematic Reviews 2012, Issue 1. Art. No.: CD009593. DOI:
10.1002/14651858.CD009593.
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
A B S T R A C T
This is the protocol for a review and there is no abstract. The objectives are as follows:
Primary objectives
Review question A: To obtain summary estimates of the diagnostic accuracy of Xpert MTB/RIF for the diagnosis of pulmonary TB,
using solid or liquid culture as a reference standard.
Purpose of index test:
A.1 Xpert MTB/RIF as a replacement test for smear microscopy.
A.2. Xpert MTB/RIF as an add-on test after smear microscopy.
Review question B: To obtain summary estimates of the diagnostic accuracy of Xpert MTB/RIF for detection of rifampicin resistance,
using solid or liquid culture as a reference standard (
WHO 2008).
Purpose of index test:
B.1 Xpert MTB/RIF as a replacement test for WHO-approved tests for detection of rifampicin resistance.
1. To summarize evidence on time to treatment initiation.
2. To summarize evidence on time to diagnosis.
Although these secondary outcomes will not be systematically reviewed, we will extract data when present in the included accuracy
studies.
We will investigate whether HIV-infection status; sputum smear statu s; country income status; setting; or storage condition s of specimen
can explain the expected heter ogeneity in estimates of test sensitivity and specificity.
1Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
B A C K G R O U N D
Tuberculosis (TB) is one of the world’s most important infectious
causes of morbidity and mortal ity among adults. An estimated
one-third of the world’s population is infected with TB. In 2010,
there were 8.8 million new, and 12.0 million prevalent cases of
TB; 1.1 million deaths occurred among HIV-uninfected people
and an additional 0.35 million deaths among HIV-infected peo-
ple (
WHO 2011a). Of the total new TB cases, an estimated 12%
to 14% occurred among people living with HIV. Approximately
one million TB cases occur in chil dren younger than 15 years old
annually (
Marais 2010a). In 2010, the three countries with the
highest number of new TB cases were India, China, and South
Africa (
WHO 2011a). In 2010, there were an estimated 650,000
cases of multidrug-resistant TB (MDR-TB), defined as resistance
to at least isoniazid and rifampicin, the two most powerful first-
line anti-TB drugs (
WHO 2011a). TB is a treatable and curable
disease; according to the World Health Organization (WHO), up
to six million lives were saved with th e expansion of Directly Ob-
served Treatment Short-Course (DOTS; the basic package that
underpins the Stop TB Strategy) (
WHO 2010a). Early and ac-
curate diagnosis and effective treatment is the cornerstone of TB
care and control (
Dye 2010). A basic tenet of early and accurate
diagnosis is the identification of smear-negative disease (associated
with HIV infection) and MDR-TB (
WHO 2010b).
In 2011, poor diagnosis remains an obstacle to TB care and con-
trol, partly because TB diagnosis continues to rely on century-
old tests. In most TB endemic countries, TB diagnosis is based
on direct Ziehl-Neelsen sputum microscopy or chest radiography,
tests with known shortcomings, especially in people with HIV in-
fection (
Harries 2004; Perkins 2007; Steingart 2006). Mycobac-
terial cultures are time consuming and have biosafety and train-
ing requirements, and culture capacity is limited in underserved
and remote areas. Nucleic acid-amplification (NAA) tests, includ-
ing polymerase chain reaction (PCR) tests, can rapidly detect My-
cobacterium tuberculosis (M. tuberculosis), but studies of conven-
tional NAA tests have shown relatively low sensitivity in sputum
smear-negative patients (
Flores 2005; Greco 2006; Ling 2008) and
these assays can only be performed in laboratories with specialized
equipment and expertise. The disappointing performance of these
tools is compounded by the lack of access to health services with
diagnostic laboratories (WHO 2010a). A substantial proportion
(~35%) of the estimated TB cases worldwide remain undiagnosed,
including a staggering proportion (~85%) of patients with MDR-
TB (
WHO 2011a). In addition, because of delays in diagnosis,
TB patients have often been symptomatic for months, leading to
increased illness and mortality, secondary drug resistance, and on-
going transmission. Simple and rapid diagnostic tests at the point
of treatment in high-TB burden countries are urgently needed.
Target condition being diagnosed
TB is an airborne disease caused by the bacterium, M. tuberculosis,
and is spread primarily by droplet nuclei expelled by a person who
has infectious active TB. Although TB most commonly affects the
lungs, any organ or tissue may be involved. Signs and symptoms of
pulmonary TB include cough for at least two weeks, fever, chills,
night sweats, weight loss, haemoptysis (coughing up blood), and
fatigue; symptoms of extrapulmonary TB depend on the site of
disease. From 1970 to 1986, wide-scale international multicen-
tre randomized controlled trials conducted by the British Medical
Research Council and its collaborators established the pivotal role
of rifampicin in TB treatment leading to modern short-course TB
therapy (
Fox 1999). TB, even when resistant to rifampicin, can be
cured; however,to be effective, TB treatment regimens must con-
tain multiple drugs to which the organisms are susceptible. Inter-
national guidelines for the treatment of TB are issued by a WHO
Expert Group and are regularly updated. The current WHO treat-
ment guidelines are based on evidence assessed according to the
GRADE (Grading of Recommendations Assessment, Develop-
ment and Evaluation) approach for developing health care recom-
mendations (
Guyatt 2008; WHO 2009).
Index test(s)
The Xpert MTB/RIF© test is an automated PCR test utilizing the
GeneXpert© platform. Xpert MTB/RIF can detect TB as well as
rifampicin resistance in less than two hours with minimal hands-
on technical time. Xpert MTB/RIF is considered to be ground-
breaking because the test comes close to meeting the niche for a
TB point-of-care test. Unlike conventional NAA tests, this test
is unique because all steps involved in the PCR are completely
automated and self-contained, allowing the technology to be taken
out of the laboratory, into the clinic setting, where it can be used
nearer to the patient (
Small 2011).
Although, Xpert MTB/RIF provides testing for both M. tubercu-
losis and rifampicin resistance, it is really only one test. The test
uses five molecular beacons. Molecular beacons are nucleic acid
probes that recognize and report the presence or absence of the
normal, susceptible, ’wild type’ sequence of the RNA polymerase
(rpoB) gene of M. tuberculosis. When a beacon fluoresces or ’lights
up’, this indicates the presence of the gene sequence which is char-
acteristic of rifampicin-susceptible M. tuberculosis. The number of
positive beacons allows the test to distinguish among the following
results: ’No TB dete cted’ (none of the five beacons is positive);
’TB detected, rifampicin resistance de tected’ (from two to four
beacons are positive); ’TB detected, no rifampicin resistance de-
tected’ (five beacons are positive); and an ’invalid result’ (one bea-
con is positive). Xpert MTB/RIF occupies one physical unit and
uses the same sputum sample to provide results for both detection
of M. tuberculosis and rifampicin resistance. One cannot switch
rifampicin resistance testing off and only do TB testing, although
it is possible for the laboratory to omit results for rifampicin resis-
tance testing when reporting to the healthcare provider.
2Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
The physical unit for Xpert MTB/RIF has two main components:
1) a plastic cartridge containing liquid sample pr ocessing buffers
and PCR buffers and reagents; and 2) a device that controls the
fluidics inside the cartridge and performs real-time PCR analysis
(Helb 2009). The Xpert MTB/RIF assay amplifies a sequence of
the rpoB gene specific to members of M. tuberculosis complex. In
greater than 95% of M. tuberculosis clinical isolates, resistance to
rifampicin has been associated with single amino acid alterations
in a limited region (81 base pairs (bp) also called rifampicin-re-
sistance determining region of the rpoB gene (Telenti 1993). Ri-
fampicin-susceptible isolates show no mutations in this region.
With Xpert MTB/RIF, the limit of detection for M. tuberculosis
DNA was found to be 4.5 genomes per PCR reaction (95% confi-
dence interval (CI) 3.3 to 9.7) and for M. tuberculosis cells in clin-
ical sputum samples, 131 colony-forming units (cfu)/mL (95%
CI 106.2 to 176.4)
Helb 2009). In investigations using clinical or
experimental samples, all 23 81-bp mutants were correctly iden-
tified as rifampicin-resistant (
Helb 2009).
Alternative test(s)
The most widely used te st for TB diagnosis in low- and middle-
income countries is Ziehl-Neelsen smear microscopy. Sensitivity is
low (from 50 to 60% on average) and variable (from 20 to 80%),
and microscopy does not detect smear-negative TB which may
account for 24% to 61% of all pulmonary cases in HIV-infected
individuals (
Steingart 2006; Getahun 2007).
Chest radiography f or TB diagnosis is limited by high inter- and
intra-observer differences in reporting of radiographs, and absence
of typical findings in people living with HIV who have advanced
immunosuppression (
Harries 2004).
Improved diagnostic tests such as mycobacterial culture and NAA
tests are available in high-income countries, but are often too ex-
pensive and complex for routine use by TB control programmes
in resource-limited TB-endemic settings. Lack of access to diag-
nostic services in resource-limited settings presents an additional
barrier to using these tests.
Rationale
Existing diagnostic tools for TB are not accurate, or cannot be
done rapidly at the point-of-care; therefore, th ere is an urgent need
for a diagnostic tool that is accurate, simple to operate, and can be
placed nearer to the patient in facilities such as h ealth posts and mi-
croscopy centres. While rapid, simple point-of-care tests exist for
infections like HIV and malaria, there is currently no such option
for TB. Such a tool would have significant impact on TB control
through interruption of transmission and potentially earlier, more
efficient diagnosis of TB, including the detection of smear-nega-
tive disease and MDR-TB. In December 2010, WHO announced
its endorsement of the Xpert MTB/RIF test (
WHO 2011). The
WHO decision to endorse this test was based on a large multicen-
tre study (
Boehme 2010) and other preliminary data, reviewed by
an Expert Group (
WHO 2010b). These studies showed that Xpert
MTB/RIF has a comparable level of diagnostic performance to
mycobacterial culture, even in resource-limited settings. A subse-
quent implementation study (
Boehme 2011) demonstrated high
sensitivity of Xpert MTB/RIF in smear-negative patients (a con-
cern in HIV co-infected individuals, and in children) (
Mugusi
2006
; Perkins 2006; Perkins 2007), while conventional NAA tests
have low sensitivity in smear-negative patients (
Greco 2006; Ling
2008
). The WHO now recommends that Xpert MTB/RIF should
be used as the initial diagnostic test in individuals suspected of
MDR-TB or HIV-associated TB (
WHO 2010b). Furthermore,
Xpert may be used as an add-on test to microscopy in settings
where MDR-TB or HIV, or both, are of lesser concern, especially
in smear-negative patients. While several studies of Xpert MTB/
RIF have shown excellent performance, this assay has not been
fully validated in all settings. Since the WHO’s endorsement, sev-
eral new studies h ave been published on Xpert MTB/RIF, and
several other s are expected to be published shortly. At the time of
this writing, a systematic review on the diagnostic accuracy of this
new test has not been published.
O B J E C T I V E S
Primary objectives
Review question A: To obtain summary estimates of the diagnostic
accuracy of Xpert MTB/RIF for the diagnosis of pulmonary TB,
using solid or liquid culture as a reference standard.
Purpose of index test:
A.1 Xpert MTB/RIF as a replacement test for smear microscopy.
A.2. Xpert MTB/RIF as an add-on test after smear microscopy.
Review question B: To obtain summary estimates of the diagnostic
accuracy of Xpert MTB/RIF for detection of rifampicin resistance,
using solid or liquid culture as a reference standard (
WHO 2008).
Purpose of index test:
B.1 Xpert MTB/RIF as a replacement test for WHO-approved
tests for detection of rifampicin resistance.
Secondary objectives
1. To summarize evidence on time to treatment initiation.
2. To summarize evidence on time to diagnosis.
Although th ese secondary outcomes will not be systematically re-
viewed, we will extract data when present in the included accuracy
studies.
3Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Investigation of sources of heterogeneity
We will investigate whether HIV-infection status; sputum smear
status; country income status; setting; or storage conditions of
specimen can explain the expected heterogeneity in estimates of
test sensitivity and specificity.
M E T H O D S
Criteria for considering studies for this review
Types of studies
We will include primary studies that compared the results of the
index test with the reference standard. Diagnostic accuracy studies
are typically cross sectional in design. However,we will also include
randomized controlled trials and cohort studies.
Only studies that report data from which we can extract true posi-
tives (TP), true negatives (TN), false positives (FP), and false neg-
atives (FN) will be included.
We will exclude case-control studies. We will exclude studies that
are reported in abstracts.
Participants
Included participants for review question A.1 will be adults (15
years and older) suspected of having pulmonary TB or MDR-TB,
from all settings and all countries.
Included participants for review question A.2 will be adults sus-
pected of having pulmonary TB or MDR-TB that are determined
to be microscopy smear negative. In this diagnostic strategy, smear
microscopy may be performed pr ior to, or concurrently with,
Xpert MTB/RIF test.
Included participantsfor review question B will be adults suspected
of having pulmonary TB or MDR-TB, from all settings and all
countries.
Patients suspected of having MDR-TB may include patients with
a histor y of TB, patients on TB treatment for pulmonary TB
without sputum conversion, and symptomatic contacts of patients
with known MDR-TB.
Three categories of participants will be classified:
1. Definite TB - culture positive.
2. Probable TB (clinically considered as TB, culture negative).
3. Non-TB (clinically not considered as non-TB, culture
negative).
Index tests
We will include studies that evaluated the Xpert MTB/RIF assay.
Comparator tests
For review question A, we will include studies that evaluated smear
microscopy as a comparator.
Target conditions
Review question A: Active pulmonary TB.
Review question B: Rifampicin resistance.
Reference standards
Review question A: The reference standard for the diagnosis of
active pulmonary TB is solid or liquid mycobacterial culture.
Review question B: The reference standard for detection of ri-
fampicin resistance is 1) solid culture, or 2) a commercial liquid
culture system (BACTEC 460, MGIT 960, and MGIT Manual
System, Becton Dickinson, USA; BacT/ALERT MP, Biomerieux,
France; VersaTREK, Trek Diagnostic Systems, USA) (
Canetti
1963
; Laszlo 1997; WHO 2008).
Search methods for identification of studies
We will attempt to identify all relevant studies regardless of lan-
guage or publication status (published, unpublished, in press, and
ongoing).
Electronic searches
To identify all relevant studies, we will search the follow-
ing databases using the search terms and strategy described
in
Appendix 1: Cochrane Infectious Diseases Group Special-
ized Register; MEDLINE; EMBASE; ISI Web of Knowledge;
MEDION; LILACS; BIOSIS; and SCOPUS. We will also search
the metaRegister of Controlled Trials (mRCT) and the search por-
tal of the WHO International Clinical Trials Registry Platform (
www.who.int/trialsearch), to identify ongoing trials.
Searching o ther resources
We will review reference lists of included articles and any relevant
review articles identified through the above methods. We will con-
tact the test manufacturer (Ceph eid Inc.) to identify unpublished
studies. We will also handsearch WHO reports on Xpert MTB/
RIF. We will contact researchers at the Foundation for Innovative
New Diagnostics (FIND), members of th e Stop TB Partnership’s
New Diagnostics Working Group, and other experts in the field of
TB diagnostics for information on ongoing or unpublished stud-
ies.
4Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Data collection and analysis
Selection of studies
Two independent reviewers (HS and KRS) will first look at titles
and abstracts identified by electronic literature searching to iden-
tify potentially eligible studies. Any citation identified by either
reviewer during this screen (screen 1) will be selected for full-text
review. Two independent reviewers (HS and KRS) will then re-
view full-text papers (screen 2) for study eligibility using the pre-
defined inclusion and exclusion criteria. In screen 2, any discrep-
ancies will be resolved by discussion between the reviewers, or if
they are unable to resolve, by decision of a third reviewer (MP).
A list of excluded studies and their reasons for exclusion will be
maintained.
Data extraction and management
Two independent reviewers (HS and KRS) will extract a set of data
from each study using a piloted data extraction form. Based on
the pilot, the extraction form will be finalized. Two independent
reviewers (HS and KRS) will then extract data on the following
characteristics:
• Details of study: first author; publication year; case country
of residence; World Bank country income status; setting
(outpatient, inpatient, laboratory); study design; manner of
participant selection; number participants enrolled; number
participants for whom results available; industry sponsorship.
• Characteristics of par ticipants: HIV status; smear status;
history of TB.
• Target conditions: review question A: pulmonary TB;
review question B: rifampicin resistance.
• Reference standards: review question A: culture type (solid
or liquid); percentage of contaminated cultures; review question
B: the name and manufacturer of the reference standard.
• Details of index test: software version of test.
• Details of comparator: type of microscopy: light or
fluorescence; type of smear: direct or concentrated; number of
smears used to determine smear positivity.
• Details of sputum specimen: type (such as expectorated
sputum, induced sputum, bronchoalveolar lavage); condition
(fresh or frozen); definition of a positive smear.
• Details of outcomes: the number of true positives (TP),
true negatives (TN), false positives (FP), and false negatives
(FN); number of missing or unavailable test results.
Time to treatment initiation is defined as the time from specimen
collection until patient starts treatment.
Time to diagnosis is defined as the time from specimen collection
until there is an available TB result in lab or clinic, if the test was
performed in a clinic.
Country income status will be classified as low/middle-income or
high-income, according to the World Bank List of Economies.
Country income status will serve as a surrogate indicator for TB
incidence.
Review question A: Additional data about (a) proportion of inde-
terminate results, and (b) discordant results between Xpert MTB/
RIF and the reference standard (Xpert positive/culture negative
results) will be recorded.
Indeterminates
Review question A: other possible test results are invalid, error,
or no result. These results will be combined and considered as
’indeterminate’.
The pr oportion of indeterminate results will be the number of
tests classified as ’invalid’, error’, or ’no result’ divided by the total
number of tests performed.
Review question B: RIF indeterminate means that the M. tuber-
culosis concentration was very low and resistance could not be de-
termined. Proportion of indeterminate results will be the number
of tests classified as ’ indeterminate’ divided by the total number
of tests performed.
Culture contamination will be defined as 1) growth of non-TB
bacteria or fungi or 2) cross-contamination as determined after a
standard laboratory evaluation. Per centage of contaminated cul-
tures will be the (number of contaminated cultures/total number
of cultures performed) x 100.
We will contact authors of primary studies for missing data or
clarifications. All data will be entered into a database manager. A
draft data extraction form is included in
Appendix 2
Assessment of methodological quality
Two reviewers will independently assess study quality with the
modified version of Quality Assessment of Diagnostic Accuracy
Studies (QUADAS) (
Reitsma 2009). Items 1 to 11 from the
QUADAS list will be scored as yes, no, or unclear. Disagreements
will be resolved by discussion between the reviewers or by a third
reviewer (MP). Results will be described in the text and presented
graphically. Appendix 3 describes the criteria that need to be met
for each study to be rated as yes, no, or unclear for each of the
QUADAS items.
Statistical analysis and data synthesis
The first step in data analysis will be a descriptive analysis of th e
results of the primary studies. For both review question A and
review question B, the results will be based on categorical (binary)
test results. For both review questions, the index test results are
automatically generated and the user is provided with a printable
test result. Example s are:
1. MTB detected; RIF resistance not detected.
2. MTB detected; RIF resistance detected.
3. MTB detected; RIF resistance indeterminate.
4. MTB not detected; RIF not detected.
5Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Descriptive analysis will be perf ormed using Stata 2009 and key
study characteristics will be displayed in tables. For each study,
sensitivity and specificity of the test along with the 95% CI will
be calculated using exact methods, and forest plots generated us-
ing Review Manager 5 (RevMan). The primary analysis will be
performed for participants with definite TB (culture positive) and
non-TB (culture negative). Secondary analyses will estimate ac-
curacy using definite TB and probable-TB patients combined for
sensitivity calculations, and non-TB and probable TB patients
combined for specificity calculations.
For review question B, we will sort the studies in RevMan by “year
of study” to look for a trend with time, since software and cartridge
changes have been made to improve the specificity for rifampicin
detection.
Where sufficient data are available, meta-analyses will be carried
out to estimate sensitivity and specificity of the index test (primary
objective). The exact method used, either bivariate or HSROC,
will depend on data pr ovided by the included studies. For review
question A, detection of M. tuberculosis, since the test uses a com-
mon threshold for a positive result, we will use the bivariate ran-
dom effects regression model (
Macaskill 2010; Reitsma 2005).
The model will be estimated using a Bayesian approach with non-
subjective prior distributions and implemented using WinBUGS
(Version 1.4.1) (
Spiegel halter 2004).
For review question B, detection of rifampicin resistance, if most
studies report one or two and the same threshold (the same am-
plification cycle used for detection of rifampicin resistance), meta-
analysis can also be done by using the bivariate method. However,
where the studies report several different thresholds, it may be
more appropriate to use the Hierarchical Summary Receiver Op-
erating Characteristic (HSROC) model (
Rutter 2001; Macaskill
2010
).
We will also compare the sensitivity and specificity of Xpert MTB/
RIF with that of smear microcopy. For smear microscopy, the re-
sults will be based on categorical results, either positive or negative.
If most studies report one and th e same threshold (for example,
smear positive is greater than or equal to one acid-fast bacillus), we
will pool results using the bivariate method, but if studies report
several different thresholds, it may be more appropriate to use the
HSROC model (
Macaskill 2010; Rutter 2001).
Our approach to Xpert MTB/RIF used as an add-on test to smear
microscopy will be as follows: in patients found to be smear neg-
ative/culture positive for pulmonary TB, we will consider sensi-
tivity and specificity e stimates to be a proxy for Xpert MTB/RIF
used as an add-on test to microscopy, even if the primary study
objective was not explicit for this outcome and both tests were run
concurrently.
Approach to indeterminate index test results
For both review questions A and B, we will exclude indeterminate
index test results from the main analysis.
For both review questions A and B, we will determine pooled
estimates and the predicted interval for indeterminate index test
results.
For both review questions A and B, where data are available, we
will perform sensitivity analyses to determine the potential impact
of indeterminate index test results considered to be false/true pos-
itives or false/true negatives. In the discussion section, we will dis-
cuss the consequences of an indeterminate index test result con-
sidered to be a true negative result (may l ead to missed/delayed
diagnosis, with potential for increased morbidity, mortality, and
TB transmission), or considered to be true positive result (may
lead to unnecessary treatment with adverse effects and increased
anxiety).
Subgroup analyses
For both review questions A and B, we will first stratify studies
by country income status (low- and middle-income versus high-
income). We expect the majority of studies to report TP, TN, FP,
and FN stratified by smear status and/or HIV status. For these
subgroups, we will compare summary estimates of accuracy in
HIV infected and uninfected subgroups, and smear positive and
smear negative subgroups. If there are sufficient studies, we will
also determine summary accuracy estimates for smear-negative,
HIV-infected versus smear-positive, HIV-infected subgroups.
Investigations of heterogeneity
Heterogeneity between diagnostic accuracy studies is to be ex-
pected (
Harbord 2007). Initially, heterogeneity will be addressed
by pre-specifying subgroups. We will assess heterogeneity by vi-
sual inspection of forest plots. We will further investigate potential
sources of heterogeneity by adding covariates in the models. All
covariates will be study level, dichotomous.
Review question A
Condition of specimen (categorical covariate): 1. fresh; 2. frozen.
TB prevalence (categorical covariate): 1. low; 2. high.
Setting in which Xpert was used (categorical covariate): 1. clinical
(outpatient or inpatient); 2. laboratory.
Review question B
Software version (amplification cycle thresholds of the test, di-
chotomous): 1. Versions 1 and 2 (cycle threshold 3.5); 2. Versions
3 (cycle threshold 5.0) and 4.
MDR-TB prevalence (categorical covariate): 1. low; 2. high.
Sensitivity analyses
If sufficient studies are available, we will perform sensitivity anal-
ysis for QUADAS items to explore whether the results we found
are robust with respect to methodological quality of the studies.
6Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Assessment of reporting bias
Data included in this review will not allow for formal assessment
of publication bias using methods such as funnel plots or regres-
sion tests because such techniques have not been found to be help-
ful for diagnostic test accuracy studies (Tatsioni 2005 Macaskill
2010
). However, being a new test for which there is going to be
considerable attention and scrutiny, we believe reporting bias will
be minimal.
Other
We will summarize, if feasible, evidence on outcomes important
to Xpert users, including time to diagnosis and time to treatment
initiation. We will also summarize hands-on time for specimen
processing and work-flow, instrument ease-of-use, and user satis-
faction. This information will be excluded from the formal proto-
col. We will address these outcomes in a section of the discussion
and present summary data in additional tables. In addition, if data
are available, we will prepare a qualitative de scription in the dis-
cussion section of Xpert positive/culture negative (false positive)
patients followed longitudinally, and report the number and per-
cent of these patients who become culture positive during follow
up.
A C K N O W L E D G E M E N T S
We are grateful to Vittoria Lutje, Liverpool School of Tropical
Medicine, for help with the search strategy. The e ditorial base for
the Cochrane Infectious Disease Group is funded by the Depar t-
ment for International Development (DFID), UK, for the benefit
of low- and middle-income countries.
R E F E R E N C E S
Additional references
Armand 2011
Armand S, Vanhuls P, Delcroix G , Courcol R, Lemaitre
N. Comparison of the Xpert MTB/RIF test with an
IS6110-TaqMan real-time PCR assay for direct detection of
Mycobacterium tuberculosis in respiratory and nonrespiratory
specimens. Journal of Clinical Microbiology 2011;49(5):
1772–6.
Balshem 2010
Balshem H, Helfand M, Schunemann HJ, Oxman AD,
Kunz R, Brozek J, et al.GRADE guidelines: 3. Rating the
quality of evidence. Journal of Clinical Epidem iology 2010;
64(4):401–6.
Banada 2010
Banada PP, Sivasubramani SK, Blakemore R, Boehme C,
Perkins MD, Fennelly K, et al.Containment of bioaerosol
infection risk by the Xpert M TB/RIF assay and its
applicability to point-of-care settings. Journal of Clinical
Microbiology 2010;48(10):3551–7.
Blakemore 2010
Blakemore R, Story E, Helb D, Kop J, Banada P, Owens
MR, et al.Evaluation of the analytical performance of the
Xpert MTB/RIF assay. Journal of Clinic al Microbiology
2010;48(7):2495–501.
Boehme 2010
Boehme CC, Nabeta P, Hillemann D, Nicol MP, Shenai S,
Krapp F, et al.Rapid molecular detection of tuberculosis and
rifampin resistance. New England Journal of Medicine 2010;
363:1005–15.
Boehme 2011
Boehme CC, Nicol MP, Nabeta P, Michael JS, Gotuzzo
E, Tahirli R, et al.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. Lancet 2011;377(9776):
1495–505.
Canetti 1963
Canetti G, Froman S, Grosset J, Hauduroy P, Langerova M,
Mahler HT, et al.Mycobacteria: Laboratory methods for
testing drug sensitivity and resistance. Bulletin of the World
Health Organization 1963;29:565–78.
Ciftci 2011
Ciftci IH, Aslan MH , Asik G. Evaluation of Xper t MTB/
RIF results for the detection of Mycobacterium tuberculosis
in clinical samples. Mikrobiyoloji Bulteni 2011;45(1):43–7.
Dye 2010
Dye C, Williams BG. The population dynamics and control
of tuberculosis. Science 2010;328(5980):856–61.
Fendall 1972
Fendall NR. Auxiliaries a nd primary medical care. Bulletin
of the New York Academy of Medicine 1972;48(10):
1291–300.
Flores 2005
Flores LL, Pai M, Colford JM Jr, Riley LW. In-house nucleic
acid amplification tests for the detection of Mycobacterium
tuberculosis in s putum specimens: meta-analysis and meta-
regression. BMC Microbiology 2005;5:55.
Foundation
Foundation for Innovative Diagnostics. Automated
molecular detection in 90 minutes for tuberculosis
and rifampicin resistance. Available from http://
www.finddia gnostics.org/export/sites/default/media/press/pdf/
XpertTB_factsheet.pdf (accessed 7 March 2011).
Fox 1999
Fox W, Ellard G A, Mitchison D A. Studies on the
treatment of tuberculosis undertaken by the British Medical
7Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Research Council tuberculosis units, 1946-1986, with
relevant subsequent publications. International Journal of
Tuberculosis and Lung Disease 1999;3(10 Suppl 2):S231–79.
Gatsonis 2006
Gatsonis C, Paliwal P. Meta-analysis of diagnostic and
screening test accuracy evaluations: methodologic primer.
American Journal of Roentgenology 2006;187(2):271–81.
Getahun 2007
Getahun H, Harrington M, O’Brien R, Nunn P. [Diagnosis
of smear–negative pulmonary tuberculosis in people with
HIV infection or AIDS in resource–constrained settings:
informing urgent policy c hanges ]. Lancet 2007;369(9578):
2042–9.
Greco 2006
Greco S, Girardi E, Navarra A, Saltini C. Current evidence
on diagnostic accuracy of commercially based nuc leic
acid amplification tests for the diagnosis of pulmonary
tuberculosis . Thorax 2006;61(9):783–90.
Guyatt 2008
Guyatt GH, Oxman AD, Kunz R, Falck-Ytter Y, Vist GE,
Liberati A, et al.Going from evidence to recommendations.
BMJ 2008;336(7652):1049–51.
Harbord 2007
Harbord RM, Deeks JJ, Egger M , Whiting P, Sterne JA.
A unification of models for meta-analysis of diagnostic
accuracy studies. Biostatistics 2007;8(2):239–51.
Harries 2004
Harries A. [16. How does the diagnosis of tuberculosis in
persons infected with HIV differ from diagnosis in persons
not infected with HIV?]. In: Frieden T editor(s). Toman’s
Tuberculosis. Case detection, treatment and monitoring -
questions and answers. 2nd Edition. Geneva: World Health
Organization, 2004:80–3.
Helb 2009
Helb D, Jones M , Story E, Boehme C, Wallace E, Ho K,
et al.Rapid detection of Mycobacterium tuberculosis and
rifampin resistance by use of on-demand, near-patient
technology. Journal of Clinical Microbiology 2009;48(1):
229–37.
Hesseling 2011
Hesseling AC, Graham SM, Cuevas LE. Rapid molecular
detection of tuberculosis. New England Journal of Medicine
2011;364(2):183–5.
Hillemann 2011
Hillemann D, Ruesch-Gerdes S, Boehme C, Richter E.
Rapid molecular detection of extrapulmonary tuberculosis
by automated GeneXpert(R) MTB/RIF system. Journal of
Clinical Microbiology 2011;49(4):1202–5.
Laszlo 1997
Laszlo A, Rahman M, Raviglione M, Bustreo F. Quality
assurance programme for drug susceptibility testing
of Mycobacterium tuberculosis in the WHO/ IUATLD
Supranational Laboratory Network: first round of
proficiency testing. International Journal of Tuberculosis and
Lung Disease 1997;1(3):231–8.
Leeflang 2008
Leeflang MM, Deeks JJ, Gatsonis C, Boss uyt PM.
Systematic reviews of diagnostic test accuracy. Annals of
Internal Medicine 2008;149(12):889–97.
Lijmer 2002
Lijmer JG, Bossuyt PM, Heisterkamp SH . Exp loring
sources of heterogeneity in systematic reviews of diagnostic
tests. Statistics in Medic ine 2002;21(11):1525–37.
Ling 2008
Ling DI, Flores LL, Riley LW, Pai M. Commercial
nucleic-acid amplification tests for diagnosis of pulmonary
tuberculosis in respiratory specimens: meta-analysis and
meta-regression. PLoS One 2008;3(2):e1536.
Macaskill 2010
Macaskill P, Gatsonis C, Deeks JJ, Harbord RM, Y
Takwoingi. [Chapter 10: Analysing and Presenting Results.
In: Deeks JJ, Bossuyt P M, C Gatsonis (editors). Cochrane
Handbook for Systematic Reviews of Diagnostic Test
Accuracy Version 1.0. The Cochrane Collaboration 2010].
Available from http://srdta.cochrane.org/.
Malbruny 2011
Malbruny B, Le Marrec G, Courageux K, Leclercq R,
Cattoir V. Rapid and efficient detection of Mycobacterium
tuberculosis in respiratory and non-respiratory samples.
International Journal of Tuberculosis and Lung Disease 2011;
15(4):553–5.
Marais 2010
Marais BJ, Gupta A, Starke JR, El Sony A. Tuberculosis in
women and children. Lancet 2010;375(9731):2057–9.
Marais 2010a
Marais BJ, Schaaf HS. Childhood tuberculosis: an emerging
and previously neglected problem. Infect Disease Clinics of
North America 2010;24(3):727–49.
Marlowe 2011
Marlowe EM, Novak Weekley SM, Cumpio J, Sharp
SE, Momeny MA, Babst A, et al.Evaluation of the
Cepheid Xpert MTB/RIF assay for the direct detection
of Mycobacterium tuberculosis complex from respiratory
specimens. Journal of Clinical Microbiology 2011;49(4):
1621–3.
Moher 2009
Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred
reporting items for systematic reviews and meta-analyses:
the PRISMA statement. PLoS Medicine 2009;6(7):
e1000097.
Moure 201 1
Moure R, Munoz 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. Journal of
Clinical Microbiology 2011;49(3):1137–9.
Mugusi 2006
Mugusi F, Villamor E, Urassa W, Saathoff E, Bosch RJ,
Fawzi WW. H IV co-infection, CD4 cell counts and clinical
correlates of bacillary density in pulmonary tuberculosis.
8Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
[...]... A (detection of MTB) and/ or B (detec- 1 - A tion of RIF resistance) ? 2-B 3 - A and B What was the purpose of this study? * if smear results are stratified, 1 - Only accuracy of Xpert as replacement test for microscopy? indicate #3 2 - Only accuracy of Xpert as add-on test to microscopy (include studies that evaluate incremental value of Xpert to the index test) ? 3 - Both purposes, 1 and 2 Xpert MTB/RIF. .. publication for the study APPENDICES Appendix 1 Detailed search strategies 1 Xpert* .tw 2 GeneXpert*.tw 3 Cepheid.tw 4 near* patient ti, ab 5 or 1-4 6 Tuberculosis/ 7 exp Tuberculosis, Pulmonary/ 8 exp Tuberculosis, Multidrug-Resistant/ 9 Mycobacterium tuberculosis/ 10 TB.tw 11 tuberculosis. tw 12 or/6-11 13 5 and 12 14 limit 13 to yr=“2007 -Current” Xpert MTB/RIF test for detection of pulmonary tuberculosis and. .. 2000;4(5):481–4 Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol) Copyright © 2012 The Cochrane Collaboration Published by John Wiley & Sons, Ltd 9 Van Rie 2010 Van Rie A, Page-Shipp L, Scott L, Sanne I, Stevens W Xpert ((R)) MTB/RIF for point -of- care diagnosis of TB in highHIV burden, resource-limited countries: hype or hope? Expert Review of Molecular Diagnostics... Total Indeterminate Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol) Copyright © 2012 The Cochrane Collaboration Published by John Wiley & Sons, Ltd 17 Question A: MTB Detection, HIV Negative Definite TB Yes Index Test Result No Total Positive Negative Total Indeterminate Question B: RIF Resistance Confirmed rifampicin resistance Yes Index Test Result No Total... the same time or within 30 days of each other (Ideally Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol) Copyright © 2012 The Cochrane Collaboration Published by John Wiley & Sons, Ltd 19 (Continued) specimens for Xpert and culture are collected on the same patients at the same time However, if this is not possible and a delay of several weeks occurs between... reference test Unclear if not enough information is provided for judgment Were the Xpert results interpreted without knowledge of reference Yes for all studies Xpert is a fully automated system that provides standard results a print out of test results Relevant clinical information Yes for all studies In this review the availability or absence of clinical information such as age and presence and severity of. .. TABLES Question A: MTB Detection, Overall Definite TB * Only extract if not reporting by smear status Yes Index Test Result No Total No Total Positive Negative Total Indeterminate Question A: MTB Detection, Smear Definite TB Positive Yes Index Test Result Positive Negative Total Indeterminate Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol) Copyright © 2012... Comments: Discrepant analysis Criteria Number Xpert+ /culture - baseline Deemed TB after further evaluation Percent found to be TB on discrepant analysis * Follow-up test included, circle all that apply ** Repeat culture, DNA sequencing, GenoType® MTBDRplus test, other, describe Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol) Copyright © 2012 The Cochrane Collaboration... al .Detection of rifampicin- resistance mutations in Mycobacterium tuberculosis Lancet 1993;341 (8846):647–50 Traore 2000 Traore H, Fissette K, Bastian I, Devleeschouwer M, Portaels F Detection of rifampicin resistance in Mycobacterium tuberculosis isolates from diverse countries by a commercial line probe assay as an initial indicator of multidrug resistance International Journal of Tuberculosis and. .. index and reference tests Unclear if not enough information is provided Differential verification avoided? Yes if all participants received the same reference test regardless of Xpert results No if different reference tests were used depending on Xpert results Unclear if not enough information is provided for judgment Incorporation avoided Yes for all studies Xpert does not form part of the reference standard . counts and clinical
correlates of bacillary density in pulmonary tuberculosis.
8Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance. value of Xpert to the
index test) ?
3 - Both purposes, 1 and 2
1 1Xpert MTB/RIF test for detection of pulmonary tuberculosis and rifampicin resistance (Protocol)
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