While many North American healthcare institutions are switching from Tuberculin Skin Test (TST) to Interferon-gamma release assays (IGRAs), there is relatively limited data on association between occupational tuberculosis (TB) risk factors and test positivity and/or patterns of test discordance.
We recruited a cohort of Canadian health care workers (HCWs) in Montreal, and performed both TST and QuantiFERON-TB Gold In Tube (QFT) tests, and assessed risk factors and occupational exposure.
In a cross-sectional analysis of baseline results, the prevalence of TST positivity using the 10 mm cut-off was 5.7% (22/388, 95%CI: 3.6–8.5%), while QFT positivity was 6.2% (24/388, 95%CI: 4–9.1%). Overall agreement between the tests was poor (kappa = 0.26), and 8.3% of HCWs had discordant test results, most frequently TST−/QFT+ (17/388, 4.4%). TST positivity was associated with total years worked in health care, non-occupational exposure to TB and BCG vaccination received after infancy or on multiple occasions. QFT positivity was associated with having worked as a HCW in a foreign country.
Our results suggest that LTBI prevalence as measured by either the TST or the QFT is low in this HCW population. Of concern is the high frequency of unexplainable test discordance, namely: TST−/QFT+ subjects, and the lack of any association between QFT positivity and clear-cut recent TB exposure. If these discordant results are indeed false positives, the use of QFT in lieu of TST in low TB incidence settings could result in overtreatment of uninfected individuals.
Citation: Zwerling A, Cojocariu M, McIntosh F, Pietrangelo F, Behr MA, et al. (2012) TB Screening in Canadian Health Care Workers Using Interferon-Gamma Release Assays. PLoS ONE 7(8): e43014. doi:10.1371/journal.pone.0043014
Editor: Marc Tebruegge, The University of Melbourne & The Murdoch Childrens Research Institute & The Royal Children's Hospital Melbourne, Australia
Received: May 31, 2012; Accepted: July 16, 2012; Published: August 20, 2012
Copyright: © Zwerling et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the Canadian Institutes of Health Research (CIHR) grant 81362. AZ received a doctoral fellowship from CIHR, and MP received a New Investigator Award from CIHR. MP also received a salary award from Fonds de recherche du Québec–Santé. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: MP serves on the editorial boards of PLoS One and PLoS Medicine. He is a Section Editor with PLoS One. MB is co-author of a United States patent on molecular differences between species of the Mycobacterium tuberculosis complex. U.S. patent filed May 25, 1999 Bozicevic, Field and Francis, LLP, Palo Alto, CA, 94301. Serial number 09/313,191. Issued as U.S. patent 6,291,190 B1 October 2001. This does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials.
Fuelled by the HIV epidemic, the emergence of multi- and extensively drug resistant tuberculosis (MDR & XDR-TB) and an increasingly mobile population, tuberculosis (TB) continues to be a global concern and a serious risk to health care workers (HCW) worldwide , , , , . In many high income countries, HCWs are screened at regular intervals for Latent TB Infection (LTBI) in an effort to identify new infections that can be targeted for preventive therapy , , .
Traditionally TB screening in HCWs has been conducted using the Tuberculin Skin Test (TST), a test with known limitations , , . Recently, Interferon gamma release assays (IGRAs) are being increasingly used for LTBI screening. Several systematic reviews have suggested that IGRAs are as sensitive, and more specific than the TST in identifying LTBI, particularly in low TB incidence settings , , , . However, the use of IGRAs for routine screening of HCWs remains an area of controversy, and the Canadian guidelines among others have not endorsed IGRAs for serial testing in this population , . Despite this, the use of IGRAs in routine screening of HCWs is increasing, and with it, a large number of studies have reported high within subject variability, high rates of discordant test results and high rates of conversions and reversions among HCWs screened with these novel assays , .
We recruited HCWs from a low TB incidence setting into a prospective longitudinal cohort, in which HCWs are undergoing annual testing with TST and QFT. At intake into this cohort all participants underwent baseline testing. Primary objectives of this analysis were a) to assess the association between test positivity and occupational TB exposure in a cohort of Canadian HCWs; and b) to assess the association between patterns of test discordance and occupational TB exposure and other TB risk factors.
Materials and Methods
Study Setting & Population
This study was conducted at the McGill University Health Centre (MUHC), a university affiliated hospital network that employs over 11,500 health care and other personnel at seven hospitals in Montreal. TB incidence is low in Quebec with an annual incidence rate of 2.5 per 100,000 persons. Over the past decade, approximately 100–150 active TB cases have been reported annually on the island of Montreal, an incidence rate of approximately 7.1/100 000 persons per year .
HCWs at the MUHC undergo TB screening both as part of pre-employment health evaluations and through regular occupational health and safety monitoring. The majority of employees are to be screened for LTBI on an annual schedule, while those in high risk settings such as mycobacteriology laboratories are screened every 6 months. TB screening of MUHC HCWs has been traditionally done using the TST and is conducted by the Department of Occupational Health and Safety (OHS).
Study Design & Ethics approval
HCWs were approached for participation in the study at their TB screening visit with the OHS. In order to be eligible for the study, participants must have been due for scheduled TB screening, and could not have had a positive TST (≥10 mm induration) in the past. Therefore, ‘baseline testing’ refers to the first measurement for this study; for some participants this was their first ever TST, while others had been undergoing annual occupational TB screening, with negative test results in the past. HCWs who provided written informed consent were recruited to our prospective longitudinal cohort, and are now being followed and tested annually with both the TST and QFT.
At the baseline study visit, the blood draw was first performed for the QFT test, and subsequently the TST was placed. Finally, HCWs completed an interviewer-facilitated questionnaire covering occupational and non-occupational TB exposure. The study was approved by the ethics review board of the MUHC.
Tuberculin Skin Test
The TST was performed using the Mantoux method by a trained nurse hired by the research study; 5TU (0.1) ml of Tubersol PPD (Aventis Pasteur) was used, and results read as per the Canadian TB Standards . In cases where the HCW had not been tested with the TST within the last 10 years, a 2 step TST was performed if the initial result was negative (<10 mm). Upon initial testing, an induration of ≥10 mm was considered positive , .
Interferon-gamma release assay testing
The QuantiFERON-TB Gold In-Tube test (QFT) (Cellestis Ltd/Qiagen, Carnegie, Australia) was performed as per the manufacturer's instructions in a research lab at the Montreal General Hospital. The QFT result was considered positive if the interferon-gamma response in the TB antigen tube minus the response in the nil tube was ≥0.35 IU/ml as per the manufacturer's guidelines. Quantitative values of IFN-gamma were also recorded; as per manufacturer's suggestions all values greater than 10 were truncated at 10.
Ascertainment of TB Exposure
HCWs completed a questionnaire covering demographics, travel history, training and work history in health care, health care work in foreign countries, potential non-occupational exposure to TB, and potential exposure to TB in the occupational environment. Known occupational exposures are charted in the personnel files maintained by the Department of Occupational Health and Safety.
While there is no gold standard for LTBI, we hypothesized that a higher level of exposure to TB correlates with a higher probability of infection. We identified key occupational exposures based on a priori risk factors including: a) unprotected exposure to a smear positive infectious TB patient, b) direct contact with TB patients, c) type of HCW, and d) years worked in health care .
Management of Positive Results
As per the current MUHC policy, participants with a positive TST result were referred for chest x-ray plus clinical evaluation by a pulmonologist. When judged appropriate, LTBI treatment was recommended by the pulmonologist. The same process applied to participants with a positive QFT result, regardless of the accompanying TST result.
All analyses were performed with Stata, version 11 (Stata Corp, Texas, USA). Percent agreement and kappa statistics, were calculated to estimate test concordance. To assess the association between test positivity (separately for TST and QFT) and the occupational exposure variables of interest, we performed multivariable logistic regression. Variable selection for the model was done using a priori clinical knowledge. The association between risk factors and the joint patterns of TST and QFT results was assessed by nominal multinomial logistic regression. Four patterns were assessed: concordant negatives (base or reference outcome), concordant positives, discordant QFT+/TST− and discordant QFT−/TST+. Odds ratios and their accompanying 95% confidence intervals were estimated from the multivariable polytomous logistic regression model.
From May 2007 to December 2011, we approached 638 HCWs who had been referred for TST. Three hundred and ninety seven HCWs (62%) provided informed consent, completed the questionnaire, and underwent study testing procedures. Most common reasons for non-participation were lack of time, dislike of needles and/or of blood draw. Incomplete and invalid tests were excluded (including tests which could not be performed due to processing or laboratory errors. Completed questionnaires, and valid test results were available for 388 HCWs.
Among the 388 study participants with complete results, 87.9% (341/388) had had a prior TST planted either through routine TB screening at the MUHC or at another location prior to employment at the MUHC (but not within the preceding 3 months), 41/388 (11.3%) had never had TST performed previously while 6/388 (1.6%) could not recall. A second step TST was performed on 41 TST naïve HCWS and 59 HCWs who had not been tested with TST within the last ten years. Among those previously tested, 332/341(97.4%) had documented TST negative while 9/341 (2.6%) had been previously tested with TST but had never been read.
Participant Demographics & TB Exposure
Participant characteristics are displayed in Table 1. The majority of HCWs were female (288/388, 74%) and the median age was 34.4 years (Inter-quartile range, IQR: 26.9–44.7 years). The majority were Canadian-born non-aboriginal (272/388 70%), and the majority of foreign born participants (86/114, 75%) had arrived in Canada more than 5 years prior to study enrolment. HCWs had worked a median of 5 years (IQR 2- 12 years) in the health care services sector. Prior BCG vaccination was reported by 36.1% (140/388) of the cohort.
The median number of years since the last TST prior to study recruitment was 2.2 years, (IQR: 1.4–3.6 yrs) and the median number of TST tests performed prior to study enrollment was 2, (IQR:1–3) with some OHS charts reporting up to 14 TST tests per HCW.
Baseline test positivity
The prevalence of TST positivity using the 10 mm cut-off was estimated to be 5.7% (22/388, 95%CI: 3.6–8.5%), while QFT positivity was 6.2% (24/388, 95%CI: 4–9.1%), with only one indeterminate QFT result. Quantitative TST results ranged from 0 to 25 mm. When appropriate, two step TST was performed, and in 5/100 (5%) cases HCWs became TST positive upon second step testing, these HCWs were referred for follow-up but were not considered positive for subsequent analyses. QFT results (TB Ag- nil) ranged from 0–10 IU/ml. All HCWs with positive TST results were referred to see a pulmonologist, however in 7 cases, HCWs did not make a follow-up appointment. Treatment was recommended in 7/15 (46.7%) HCWs; 5 completed therapy, while 2 refused treatment. Treatment was not recommended in the remaining 8 HCWs, either due to concerns with drug interactions (n = 1), age over 35 years (n = 2) or because they were considered false-positives (n = 5).
Positivity estimates stratified by prior TST status, test type, BCG vaccination status, and country of birth are displayed in Table 2. Among those with no prior TST history, the QFT positivity rate was 4.9% (2/41, 95%CI: 0.6–16.5%) while the TST rate was almost twice that at 9.8% (4/41, 95%CI: 2.7–21.9%). When restricted to those with prior negative TST the test positivity rates for both tests decreased and the rate for QFT positivity became almost 2 percentage points higher than that of TST. Among BCG vaccinated HCWs, test positivity was slightly lower for QFT than TST.
Concordance between quantitative TST and QFT results is displayed in Figure 1. Three hundred and forty-eight (89.7%) HCWs were found to be negative by both tests, while 7 (1.8%) were concordant positives (lower left and upper right hand quadrants of Figure 1). TST positive/QFT negative discordant results were found in 15/388 cases (3.9%) and TST negative/QFT positive in 17/388 cases (4.4%).
*2 points not visible on graph: a)TST = 0, IFN-g = 10 & b)TST = 17, IFN-g = 10.
Among those with no history of BCG vaccination, only 3/248 (1.2%) were TST+/QFT− discordant, while 10/248 (4%) were TST−/QFT+ discordant. Among the BCG vaccinated, a much higher rate of TST+/QFT− discordance was observed (12/140 ,8.6%), compared to TST−/QFT+ discordance (7/140 ,5%). Overall agreement between the tests was 91.7% with a kappa value of 0.26 which can be interpreted as fair to poor agreement , . When the analysis was restricted to only those HCWs with BCG vaccination, the agreement decreased slightly to 86.3%, while the kappa value improved slightly to 0.3.
As seen in Figure 1, only 4 points (1 not shown) suggest clearly concordant positive results, while the remaining points (although still concordantly positive are close to the QFT positivity cut-off both among concordant positives and discordant TST+/QFT−. There was no statistically significant difference between the median IFN-gamma value among concordant positives (median:2.6, IQR:0.55–2.97) and among the discordant QFT +/TST negatives (median: 0.69, IQR:0.47–2.74).
When we considered a more stringent cut-off based on visual inspection of the scatterplot, we found that by employing a cut-off of 1.0 IU/ml for the QFT test , 13 HCWs would be reclassified as QFT negative; among these, 3/13 (23%) were TST positive leading to a lower QFT positivity rate of 11/388 (2.8%). This reclassification would lead to a TST+/QFT− discordance rate of 4.6% while the TST−/QFT+ discordance rate would decrease to 1.8%.
Multivariable logistic regression
The final multivariable model included the following independent variables: age, sex, non-occupational TB exposure (yes/no), birth in a country with high TB incidence, type of health care work (nurse, doctor, clinical staff, lab staff or nonclinical support staff), Total years worked and or spent training in health care, Travel more than one month outside Canada, worked as aHCW in a foreign country, BCG vaccination at birth or unknown timing, BCG vaccination post-infancy or multiple BCG vaccinations, self-reported exposure to active TB patients, documented occupational exposure to TB, age at immigration, birth outside of Canada, and finally prior negative TST (Table 3).
In the final model, non-occupational exposure to TB (OR = 11.7, 95%CI: 2.5–55.7), total years worked in health care (OR = 1.09 for every additional year, 95%CI: 1.003–1.2), BCG vaccination after infancy and or multiple BCG vaccinations (OR = 23.05, 95%CI:3.9–135.2) were all statistically significantly associated with TST positivity. Prior negative TST (OR = 0.065, 95%CI: 0.01–0.3) had a strong inverse association with TST positivity in the present study. The only variable to be statistically significantly associated with QFT positivity was having worked as a HCW in a foreign country (OR = 6.44, 95%CI: 1.6–25.0), (Table 3).
We performed a stratified analysis of only those HCWs with previous negative TST. Among this group, we found the same significant variables associated with TST positivity in the multivariable regression with the exception of total years worked in health care was no longer significant in the model. This suggests that the cumulative risk of years working in health care is not a significant predictor among those who have been routinely screened in this context.
Patterns of discordance and their association with TB risk factors
Using a multinomial logistic regression model we assessed the potential association between risk factors and 4 patterns of test concordance/discordance: concordant negatives, concordant positives, and two types of discordance: QFT+/TST− and QFT−/TST+. All outcomes were compared to the base outcome of concordant negatives (Table 4). In multivariable analysis the only three variables significantly associated with concordant positive results were BCG vaccination after birth and/or multiple vaccinations (OR = 36.32, 95%CI: 1.73–761.31), having worked in a foreign country as a HCW (OR = 30, 95%CI: 1.34–669.8), and prior negative TST, which showed a statistically significant protective effect (OR = 0.02 95%CI: 0.001–0.57)
No variables were statistically significantly associated with QFT+/TST− discordance; possibly due to the very small sample size (n = 17). Several variables were associated with QFT−/TST+ discordance, including non-occupational TB exposure (OR = 28.14 96%CI: 3.08–257.03), BCG vaccination at birth/timing unknown (OR = 19.24, 95%CI:1.29–287.21) BCG vaccination after birth and/or multiple vaccinations (OR = 63.02, 95%CI: 3.71–1069.35), Total years spent working in health care (OR = 1.23, 95%CI: 1.06–1.42), age at immigration (per year increase among foreign-born), (OR = 1.15, 95%CI:1.03–1.3) and finally inverse protective effect of prior negative TST (OR = 0.08, 95%CI: 0.01–0.60).
Results from this cohort of Canadian HCWs suggest that the prevalence of positivity for LTBI, as measured by either the TST or the QFT, in this population, is low. Furthermore, many HCWs had discordant test results, where the prognosis and treatment recommendations remain unclear.
Infrequent test positivity (using either test) and weak concordance, may suggest that the noise level (or non-specific responses) from these tests in a low TB incidence setting may be such that the true signal (ie: immunological responses indicating LTBI) is difficult to distinguish. Non-specific variation has been shown to occur in both tests, and despite being health care workers, this cohort remains a low risk population , . One alternative but not mutually exclusive hypothesis suggests these tests may be measuring independent immunological processes. Unfortunately, these hypotheses are difficult to test in the absence of a gold standard for LTBI.
Unlike many IGRA studies in HCWs, QFT did not estimate a lower positivity rate overall compared with the TST in this cohort . Comparable positivity rates have been reported from HCW studies in the United States and Italy, and may be more frequent in cohorts with low BCG vaccination , . The nature and profile of this particular HCW cohort is an important factor; MUHC HCWs with prior positive TST results do not undergo routine screening, and were therefore excluded. This leads to an underestimation of the overall prevalence of positive TST results among MUHC HCWs undergoing regular screening. When restricted to those HCWs who were TST naive, we found a positivity rate two-fold higher using the TST compared with QFT (9.8% vs. 4.9%). Although this did not reach statistical significance, it is consistent with earlier studies from low TB incidence countries . Similar results have been reported in other North American HCW cohorts, including a conference abstract by Dorman et al., where they reported on a large multi-center study including 1,313 HCWs from the United States . Both IGRAs: the QFT and the TSPOT.TB test were performed, as well as the TST, and positivity rates were 5.3%, 6.9% and 6.8% respectively. Highlighting both the low overall positivity and comparable rates estimated by the IGRAs and the TST among low risk populations.
TST+/QFT− discordant results are often attributed to BCG vaccination. In this cohort, the low level of BCG vaccination (36.1%) may lead to more comparable positivity rates between the two tests. The effect of BCG was evident when restricted to vaccinated HCWs, the TST rate increased by two fold to 12.9% while the QFT rate saw a smaller increase to 9.3%. Rates for both types of discordance remained high, and while TST+/QFT− discordance was associated with non-occupational exposure, years worked in health care, and BCG vaccination, TST−/QFT+ discordance could not be explained by any of the variables we assessed.
Results from the multivariable analysis assessing the association between LTBI risk factors and TST positivity were consistent with previous studies . Given the non-specific nature of the TST, and its known cross-reactivity with BCG vaccinated persons, we are not surprised by the strong association with BCG when vaccination was performed later in life and/or repeated. Similarly, ‘total years worked in health care’ has been shown in several studies in HCWs to be consistently associated with TST positivity .
The association of positive TST results with self-reported non-occupational exposure was unexpected in our low TB incidence setting. However, this effect was strong and consistent across analyses, indicating non-occupational exposure to TB may continue to play an important role. Conversely, known occupational exposure to TB was not significantly associated with positive results for either test. It may be that most potential hospital source cases were appropriately diagnosed and isolated, effectively reducing nosocomial transmission. Non-occupational TB exposure may also imply longer duration plus lack of proper ventilation and infection control measures, resulting in a higher likelihood of transmission. Finally, known occupational exposures may be less likely to result in transmission than are undetected hospital exposures, which neither participants nor Occupational Health & Safety can report. QFT positivity was associated significantly with just one variable: having worked as a HCW in a foreign country, which could be a proxy for high risk exposure to TB. This variable was also significantly associated with concordant positive results, suggesting these cases may be true LTBI and not false positives.
It has been hypothesized that the TST is more likely to remain positive over time compared with the QFT, which may be a more dynamic test and has been shown to have high rates of reversions upon repeat testing . It is therefore possible that TST positivity tends to be associated with cumulative TB exposure, while QFT positivity may be more linked to acute exposure, and hence less likely to persist. While it is not possible to test this hypothesis using the cross-sectional data presented here, we plan to investigate this further using future longitudinal data from this cohort.
Many have suggested alternative cut-offs for the QFT might improve reproducibility, reduce subsequent reversions and improve concordance with the TST , . We evaluated two alternative cut-offs for the QFT test. Using the most stringent cut-off we found lower overall rates of discordance, noticeably a twofold decrease in TST−/QFT+ discordance compared with TST+/QFT− discordance. This result more closely reflects results from other studies which have consistently identified TST+/QFT− as the most frequent type of reported discordance .
Strengths & Limitations
Our study was conducted in a low TB incidence setting, where TB exposure can be more accurately captured. We attempted to capture all potential exposures, both in the non-occupational and in the occupational setting; unprotected exposures to active TB patients were confirmed through occupational health and safety records. It is possible that we have not captured all occupational exposures, while TB exposure is a relatively rare event at the MUHC, and is well documented in Occupational Health and Safety charts, we cannot exclude the possibility that there were unrecognized exposures for which the HCW cannot report nor would there be any note of such an exposure in their OHS charts.
Recent work has shown that IGRAs have a certain within-subject (intra-assay) variability that can be caused by a range of factors, including: variation in sample collection and processing, improper incubation and storage, as well as laboratory factors or host biology , . To address these concerns we attempted to reduce variability and further standardized sample processing and incubation times. Periodically, the assay was repeated on the same blood to assess reproducibility of results. However, we still cannot eliminate the possibility that some of the QFT results were false positives.
One significant limitation for all studies investigating diagnostic tests for LTBI is the lack of gold standard. While studies have looked at rates of disease progression in HCWs, this is not feasible in our low incidence setting where LTBI treatment is widely used .
Upon one time testing of a cohort of Canadian HCWs, we found test positivity as measured by TST or QFT was low. Of concern is the high frequency of unexplainable test discordance, namely: TST−/QFT+ subjects, and the lack of association of positive tests (especially QFT) with clear-cut recent TB exposure. In settings with low TB incidence, these dynamic tests may result in such high levels of non-specific results compared with the true underlying prevalence of LTBI that more precise tests may be required to correctly identify TB. Without a clear understanding of what underlying processes each test is measuring (ie: acute, dynamic, static), and the long-term prognosis of HCWs with discordant test results, it remains unclear how to implement QFT tests into current HCW screening programs, and what additional value they may offer over the TST.
Many thanks to all the participating MUHC HCWs for their time and interest in the study. The authors gratefully acknowledge the staff at the Occupational Health and Safety Department of the MUHC and all TB research and TB clinic staff of the Montreal Chest Institute for their time, support and cooperation.
Conceived and designed the experiments: AZ DM MB KS MP. Performed the experiments: AZ MC FM FP. Analyzed the data: AZ AB ND MP. Contributed reagents/materials/analysis tools: MB. Wrote the paper: AZ MP. Revised the manuscript: AB ND MB DM KS.
- 1. Joshi R, Reingold AL, Menzies D, Pai M (2006) Tuberculosis among health-care workers in low- and middle-income countries: a systematic review. PLoS Med 3: e494. doi: 10.1371/journal.pmed.0030494
- 2. Menzies D, Fanning A, Yuan L, Fitzgerald M (1995) Tuberculosis among health care workers. N Engl J Med 332: 92–98. doi: 10.1056/nejm199501123320206
- 3. Menzies D, Joshi R, Pai M (2007) Risk of tuberculosis infection and disease associated with work in health care settings. Int J Tuberc Lung Dis 11: 593–605.
- 4. Chan ED, Iseman MD (2008) Multidrug-resistant and extensively drug-resistant tuberculosis: a review. Curr Opin Infect Dis 21: 587–595. doi: 10.1097/qco.0b013e328319bce6
- 5. Harries AD, Zachariah R, Corbett EL, Lawn SD, Santos-Filho ET, et al. (2010) The HIV-associated tuberculosis epidemic, when will we act? The Lancet 375: 1906–1919. doi: 10.1016/s0140-6736(10)60409-6
- 6. ATS CDC (2000) Targeted Tuberculin Testing and Treatment of Latent Tuberculosis Infection. Am J Respir Crit Care Med 161: S221–S247. doi: 10.1164/ajrccm.161.supplement_3.ats600
- 7. Jensen PA, Lambert LA, Iademarco MF, Ridzon R (2005) Guidelines for preventing the transmission of Mycobacterium tuberculosis in health-care settings, 2005. MMWR Recomm Rep 54: 1–141.
- 8. Long R, Ellis E, editors (2007) Canadian Tuberculosis Standards (6th Ed.): Public Health Agency of Canada & Canadian Lung Association.
- 9. Reichman LB, Hershfield ES, editors (2000) Tuberculosis: A Comprehensive International Approach (2nd Ed.).
- 10. Farhat M, Greenaway C, Pai M, Menzies D (2006) False-positive tuberculin skin tests: what is the absolute effect of BCG and non-tuberculous mycobacteria? Int J Tuberc Lung Dis 10: 1192–1204.
- 11. Menzies D (1999) Interpretation of repeated tuberculin tests. Boosting, conversion, and reversion. Am J Respir Crit Care Med 159: 15–21. doi: 10.1164/ajrccm.159.1.9801120
- 12. Menzies D, Pai M, Comstock G (2007) Meta-analysis: new tests for the diagnosis of latent tuberculosis infection: areas of uncertainty and recommendations for research. Ann Intern Med 146: 340–354. doi: 10.7326/0003-4819-146-5-200703060-00006
- 13. Pai M, Dheda K, Cunningham J, Scano F, O'Brien R (2007) T-cell assays for the diagnosis of latent tuberculosis infection: moving the research agenda forward. Lancet Infect Dis 7: 428–438. doi: 10.1016/s1473-3099(07)70086-5
- 14. Pai M, Riley LW, Colford JM Jr (2004) Interferon-gamma assays in the immunodiagnosis of tuberculosis: a systematic review. Lancet Infect Dis 4: 761–776. doi: 10.1016/s1473-3099(04)01206-x
- 15. Pai M, Zwerling A, Menzies D (2008) Systematic review: T-cell-based assays for the diagnosis of latent tuberculosis infection: an update. Ann Intern Med 149: 177–184. doi: 10.7326/0003-4819-149-3-200808050-00241
- 16. CanadianTuberculosisCommittee (2008) Updated Recommendations on Interferon Gamma Release Assays for Latent Tuberculosis Infection. Can Commun Dis Rep 34: 1–13.
- 17. CanadianTuberculosisCommittee (2010) Recommendations on Interferon Gamma Release Assays for the Diagnosis of Latent Tuberculosis Infection - 2010 Update. Can Commun Dis Rep 36: 1–21.
- 18. Zwerling A, van den Hof S, Scholten J, Cobelens F, Menzies D, et al. (2012) Interferon-gamma release assays for tuberculosis screening of healthcare workers: a systematic review. Thorax 67: 62–70. doi: 10.1136/thx.2010.143180
- 19. van Zyl-Smit RN, Zwerling A, Dheda K, Pai M (2009) Within-subject variability of interferon-g assay results for tuberculosis and boosting effect of tuberculin skin testing: a systematic review. PLoS One 4: e8517. doi: 10.1371/journal.pone.0008517
- 20. SSSQ (2009) Épidemiologie de la Tuberculose au Quebec de 2004 a 2007
- 21. Fleiss JL (1981) Statistical methods for rates and proportions (2nd Ed.). New York: John Wiley.
- 22. Landis JR, Koch GG (1977) The measurement of observer agreement for categorical data. Biometrics 33: 159–174. doi: 10.2307/2529310
- 23. Ciaschetti A, Franchi A, Richeldi L, Rumpianesi F, Meacci M, et al. (2007) [Screening of latent tuberculosis infection in health care workers by QuantiFERON-TB and tuberculin skin test]. G Ital Med Lav Ergon 29: 406–407.
- 24. Cummings KJ, Smith TS, Shogren ES, Khakoo R, Nanda S, et al. (2009) Prospective comparison of tuberculin skin test and QuantiFERON-TB Gold In-Tube assay for the detection of latent tuberculosis infection among healthcare workers in a low-incidence setting. Infect Control Hosp Epidemiol 30: 1123–1126. doi: 10.1086/644754
- 25. Dorman S, Belknap R, Weinfurter P, Teeter L, Thomas J, et al.. (2009) Evaluation of New Interferon–Gamma Release Assays (IGRAs) in the Diagnosis of Latent Tuberculosis Infection in U.S. Health Care Workers: Baseline Testing Results. American Thoracic Society International Conference. San Diego: Am J Respir Crit Care Med. pp. A1010.
- 26. Mirtskhulava V, Kempker R, Shields KL, Leonard MK, Tsertsvadze T, et al. (2008) Prevalence and risk factors for latent tuberculosis infection among health care workers in Georgia. The International Journal of Tuberculosis and Lung Disease 12: 513–519.
- 27. Ringshausen FC, Schablon A, Nienhaus A (2012) Interferon-gamma release assays for the tuberculosis serial testing of health care workers: a systematic review. J Occup Med Toxicol 7: 6. doi: 10.1186/1745-6673-7-6
- 28. Veerapathran A, Joshi R, Goswami K, Dogra S, Moodie EE, et al. (2008) T-cell assays for tuberculosis infection: deriving cut-offs for conversions using reproducibility data. PLoS One 3: e1850. doi: 10.1371/journal.pone.0001850
- 29. Ringshausen FC, Nienhaus A, Torres Costa J, Knoop H, Schlosser S, et al. (2011) Within-subject variability of Mycobacterium tuberculosis-specific gamma interferon responses in German health care workers. Clin Vaccine Immunol 18: 1176–1182. doi: 10.1128/cvi.05058-11
- 30. Joshi R, Narang U, Zwerling A, Jain D, Jain V, et al. (2011) Predictive value of latent tuberculosis tests in Indian healthcare workers: a cohort study. Eur Respir J 38: 1475–1477. doi: 10.1183/09031936.00014611