Volume 26, Number 8—August 2020
CME ACTIVITY - Synopsis
Tuberculosis in Internationally Displaced Children Resettling in Harris County, Texas, USA, 2010–20151
Introduction
Medscape CME ACTIVITY
In support of improving patient care, this activity has been planned and implemented by Medscape, LLC and Emerging Infectious Diseases. Medscape, LLC is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
Medscape, LLC designates this Journal-based CME activity for a maximum of 1.00 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 1.0 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit.
All other clinicians completing this activity will be issued a certificate of participation. To participate in this journal CME activity: (1) review the learning objectives and author disclosures; (2) study the education content; (3) take the post-test with a 75% minimum passing score and complete the evaluation at http://www.medscape.org/journal/eid; and (4) view/print certificate.
Release date: July 17, 2020; Expiration date: July 17, 2021
Learning Objectives
Upon completion of this activity, participants will be able to:
• Distinguish recommendations from the Centers for Disease Control and Prevention regarding screening for tuberculosis (TB) among immigrant children
• Identify rates of discrepancy between results of the tuberculin skin test and interferon-gamma release assays in the current study
• Analyze results of TB testing among immigrant children in the current study
• Evaluate risk factors for a positive TB test among immigrant children
CME Editor
Deborah Wenger, MBA, Copyeditor, Emerging Infectious Diseases. Disclosure: Deborah Wenger, MBA, has disclosed no relevant financial relationships.
CME Author
Charles P. Vega, MD, Health Sciences Clinical Professor of Family Medicine, University of California, Irvine School of Medicine, Irvine, California. Disclosure: Charles P. Vega, MD, has disclosed the following relevant financial relationships: served as an advisor or consultant for Johnson & Johnson Pharmaceutical Research & Development, LLC; GlaxoSmithKline; served as a speaker or a member of a speakers bureau for Genentech; GlaxoSmithKline.
Authors
Charles P. Vega, MD, Health Sciences Clinical Professor of Family Medicine, University of California, Irvine School of Medicine, Irvine, California. Disclosures: Gabriella S. Lamb, MD, MPH; Andrea T. Cruz, MD, MPH; Elizabeth A. Camp, PhD; Michelle Javier, MD; Jessica Montour, MPH; Tamisha Piper MPAS, PA-C; and Umair A. Shah, MD, MPH, have disclosed no relevant financial relationships. Jeffrey R. Starke, MD, has disclosed the following relevant financial relationships: served as an advisor or consultant for Otsuka Pharmaceuticals.
Abstract
US guidelines have recommended testing children emigrating from high tuberculosis-incidence countries with interferon-gamma release assays (IGRAs) or tuberculin skin tests (TSTs). We describe the Harris County (Texas) Public Health Refugee Health Screening Program’s testing results during 2010–2015 for children <18 years of age: 5,990 were evaluated, and 5,870 (98%) were tested. Overall, 364 (6.2%) children had >1 positive test: 143/1,842 (7.8%) were tested with TST alone, 129/3,730 (3.5%) with IGRA alone, and 92/298 (30.9%) with both TST and IGRA. Region of origin and younger age were associated with positive TST or IGRA results. All children were more likely to have positive results for TST than for IGRA (OR 2.92, 95% CI 2.37–3.59). Discordant test results were common (20%) and most often were TST+/IGRA– (95.0%), likely because of bacillus Calmette-Guérin vaccination. Finding fewer false positives supports the 2018 change in US immigration guidelines that recommends using IGRAs for recently immigrated children.
The World Health Organization (WHO) has estimated that there were 1 million tuberculosis (TB) cases and 234,000 tuberculosis-related deaths among children in 2017 (1). An estimated additional 67 million children were infected with Mycobacterium tuberculosis (2). Testing of children emigrating from high- to low-incidence countries can provide benefit to individual patients and to the community by identifying patients for whom providing treatment would reduce the risk of progression to disease and thus decrease the reservoir for future contagious disease cases.
Not all recently arrived children are at equal risk for TB infection. Refugees, asylees, and victims of human trafficking (VHTs) may be at highest risk as the result of prolonged periods of displacement, undernutrition, poor sanitation, and poor access to medical care (3). In the United States, special immigrant visa (SIV) holders are predominantly children of persons from Afghanistan or Iraq who served as military translators and do not typically live in congregate settings (4,5), potentially placing them at lower risk for TB exposure. Those with parole classification most commonly emigrated from Cuba, a country with a low incidence of TB (6–8).
In 2018, the Centers for Disease Control and Prevention (CDC) updated the preimmigration guidelines for TB testing for immigrants to the United States, recommending that children 2–14 years of age who come from high TB-incidence countries (>20 cases/100,000 population) be tested with an interferon-gamma release assay (IGRA) rather than a tuberculin skin test (TST) (9). Previously, because of resource restrictions, TSTs were performed more commonly in many countries, and 9%–35% of refugee children tested positive (10–15). However, in a large study, almost two thirds of children with positive preimmigration TST results had negative IGRA results on postimmigration testing (11), indicating that many positive TST results likely were caused by prior vaccination with bacillus Calmette-Guérin (BCG).
Almost 10% of refugees, asylees, parolees, or SIV holders in the United States resettle in Texas, and almost 25% of those resettle in Harris County (which includes Houston) (16). Texas is also a human trafficking hub, with many internationally trafficked persons passing through the state (17). We describe the comparative epidemiology of positive TSTs and IGRAs in children of different immigration classifications cared for through the Harris County Public Health Refugee Health Screening Program.
The Harris County Public Health Refugee Health Screening Program performs intake screening for TB, HIV, and pathogenic parasites and performs other routine laboratory screenings for all refugees, asylees, identified VHTs, parolees, and SIV holders resettling in the county. We performed a cross-sectional study of children 0–18 years of age who were evaluated by this program during January 1, 2010–December 31, 2015. We obtained demographic information, TB exposure history, symptom screening, and testing results from the Harris County Public Health Refugee Health Screening Program and the US Committee for Refugees and Immigrants (although the data originated from the Texas Department of State Health Services when the Texas Refugee Health Program resided there). All children were seen in a clinic run by the Harris County Public Health Refugee Health Screening Program. At this visit, demographic information and testing before immigration were obtained from the family and overseas records. Children not tested before immigration or who had no overseas records were tested during the clinic visit. Most of the children with a positive test for TB infection were evaluated at the Texas Children’s Hospital TB Clinic where additional testing and, if indicated, treatment were provided by 3 of the authors of this article (G.S.L., A.T.C., and J.R.S.).
Immigration classification was determined by the US Committee for Refugees and Immigrants. Immigration classifications are defined by US Citizenship and Immigration Services (Table 1) (18–22). We used WHO definitions for regions of origin (23). We predicted that refugees, asylees, and VHTs would be higher-risk groups for TB infection because they were more likely to have lived in congregate settings. We predicted the lower-risk groups to be parolees and SIVs because of their residence in lower TB-incidence nations and not living in congregate settings. Although overseas vaccination data were unavailable, we assumed that children were BCG immunized because most children emigrated from countries where universal BCG vaccination is practiced.
Clinicians in the Harris County Public Health Refugee Health Screening Program performed initial TB testing. Providers were able to choose the type of TB testing used; they typically used the TST in children <5 years of age and an IGRA in children >5 years of age (24). TST results were considered positive if there was >10 mm of induration, unless the child was living with HIV or had contact with a person with pulmonary TB, in which case the threshold was >5 mm of induration (25). The main IGRA used was the T-SPOT.TB (Oxford Immunotec, https://www.tspot.com), for which a result was defined as positive if >8 spots were noted in either well (24). A positive QuantiFERON Gold-In Tube (QIAGEN, https://www.qiagen.com) result was defined as an antigen-nil value of >0.35 IU/mL (24).
We classified children with positive test(s) for infection as TB infected, likely TB uninfected, or having TB disease. These classifications were determined by 2 authors (ATS and JRS) at the time each child was seen. In the first 2 categories, children had normal physical examinations and 2-view chest radiographs. We classified children as having TB infection if they had a positive IGRA result (IGRA+), if they had a positive TST result (TST+) and no IGRA was done (not all TST+ children had IGRAs performed), or if the IGRA result was indeterminate/invalid. We typically defined children as being likely uninfected if they were TST+/IGRA–, had normal physical examination findings and normal chest radiographs, and had no known contacts with TB disease or if they had negative tests with normal physical examination findings and chest radiographs. However, we did not classify all children who were TST+/IGRA– as being uninfected; some of these children were classified as having TB infection, most commonly because of young age (<2 years). TB disease was diagnosed in children who had clinical, physical examination, or radiographic findings consistent with TB disease (26).
We created 3 models to determine which factors were independently associated with positive tests of infection: a positive TST result, a positive IGRA result, and any positive TB test result (TST or IGRA). We compared demographic characteristics and other categorical variables among the higher-risk and lower-risk groups for statistically significant differences by the χ2 test or Fisher exact test for dichotomous variables and Wilcoxon rank-sum or Kruskal-Wallis test for continuous variables. We included any factor with a p value <0.25 in the binary regression model. We created the final model using a backward-step approach. To assess secular trends in usage and positivity, we analyzed monthly totals using linear regression and the Wilcoxon signed-rank test. A p value <0.05 was considered significant.
We conducted all analyses using the SPSS Statistics 25 (IBM, https://www.ibm.com). We obtained institutional review board approval from the Harris County Public Health Department and Baylor College of Medicine (Houston, TX, USA).
During the study period, the Harris County Public Health Refugee Health Screening Program evaluated 5,990 children (Table 2), 98% (5,870) of whom received >1 test of TB infection (Table 3): IGRA, 3,730 (63.5%); TST, 1,842 (31.4%); both TST and IGRA, 298 (5.1%). In the TST and IGRA group, 206 (69.1%) were TST–/IGRA–, 29 (9.7%) TST+/IGRA+, 57 (19.1%) TST +/IGRA–, 3 (1.0%) TST+/IGRA indeterminate/invalid, and 3 (1.0%) TST–/IGRA+ (Figure 1). Discrepant test results occurred in 60 (20.1%) children tested with both TST and IGRA.
Overall, 364 children (6.2%) had >1 positive TB test. Among these children, 325 (89.3%) received diagnoses of TB infection, 35 (9.6%) were considered likely uninfected, and 4 (1.1%) received diagnoses of TB disease (Figure 1). The 35 children with a positive test who were considered likely uninfected were all TST+/IGRA–. In addition, 22 (38.6%) children who were TST+/IGRA– were classified as having TB infection, typically earlier in the study period because of young age, variability in provider practice, or both (Figure 1).
The Texas Children’s Hospital Tuberculosis Clinic in Houston cares for most of children in Harris County with TB disease. According to a chart review, none of the children who had TB infection or who were considered likely uninfected had TB disease developed during the following 4–9 years (2,427 person-years of follow-up). Furthermore, we cross-referenced the public health records for Harris County and found that none of these children had been reported to have TB disease develop.
We found 3 factors to be associated with a either a positive TST or IGRA: region of origin, age group, and HIV status. Immigration classification was associated with a positive TB test result on univariate analysis, but this association did not hold true on multivariate analysis. Children, irrespective of immigration classification and from all regions and age groups, had greater odds of having a positive TST result than a positive IGRA result (OR 2.92, 95% CI 2.79–3.59).
Immigration Classification
On univariate analysis, irrespective of test performed, children determined to have a higher-risk immigration classification had nearly 3 times the odds of having a positive TST or IGRA compared with those with lower-risk immigration classifications (OR 2.68, 95% CI 1.94–3.68). Specifically, children with higher-risk immigration classifications had twice the odds of having a positive TST (OR 2.14, 95% CI 1.45–3.15) and nearly 4 times the odds of having a positive IGRA (OR 3.84, 95% CI 2.21–6.68) compared with children with lower-risk immigration classifications (Table 3). These differences were not seen on multivariate analysis.
All children, regardless of immigration classification, had greater odds of a positive result for TST compared with IGRA (OR 2.92, 95% CI 2.79–3.59). This difference was more pronounced among those with lower-risk classification (OR 4.81, 95% CI 2.54–9.10) than those with higher-risk classification (OR 2.68, 95% 2.15–3.35).
Region of Origin
On multivariate analysis, region of origin was a notable correlate for a positive test of TB infection. TST and IGRA positivity varied by region of origin. Using children from Southeast Asia as a reference group, we found that children from eastern Mediterranean countries (adjusted odds ratio [aOR] 0.48, 95% CI 0.33−0.70) and the Americas (aOR 0.19, 95% CI 0.09–0.39) had reduced odds for a positive TST result compared with children from Southeast Asia. Similarly, children from eastern Mediterranean countries (aOR 0.34, 95% CI 0.21−0.53) and the Americas (aOR 0.12, 95% CI 0.06–0.25) had reduced odds for a positive IGRA result compared with children from Southeast Asia (Table 4). Using the IGRA result as the reference, we found the odds of having a positive TST result to be greater in children from eastern Mediterranean countries (OR 3.99, 95% CI 2.59–6.16) and the Americas (OR 4.15, 95% CI 1.62–10.62) (Figure 2, panel A).
Age Group
TST and IGRA positivity varied by age group. Using children <2 years of age as the reference group, on multivariate analysis, we found that children 2–5 years of age had reduced odds for a positive TST result (aOR 0.40, 95% CI 0.26–0.61) and children 2–10 years of age had reduced odds for a positive IGRA result (2–5 years, aOR 0.26, 95% CI 0.11–0.60; 6–10 years, aOR 0.41, 95% CI 0.20–0.85) (Table 4).
Using the IGRA result as the reference, we found that all children, regardless of age, had greater odds of having a positive TST than a positive IGRA (OR 2.92, 95% CI 2.79–3.59). Children 6–10 years of age had the greatest odds of having a positive TST result compared with a positive IGRA result (OR 5.47, 95% CI 3.45–8.69) (Figure 2, panel B).
HIV Infection
On multivariate analysis, we found that children living with HIV had 3 times the odds for a positive TST result compared with children who were HIV uninfected (aOR 2.99, 95% CI 1.01–8.87). HIV infection was not associated with a positive IGRA result (Table 4).
In the United States, 66% of reported TB cases occur among foreign-born persons, a rate 13 times higher than for persons born in the United States (27). Previous studies, mostly using the TST, found a prevalence of TB infection of 9%–35% among refugee children (10–15). However, positive results were less common in our cohort, likely because of the variety of immigration classifications included and expanded IGRA use.
We found that the prevalence of positive results for tests of TB infection varied by region of origin and age and that all children in the study had greater odds of a positive result from TST than from IGRA. Immigration classification was not associated with positive results for TB infection. We also found discordance between TST and IGRA results across the pediatric age spectrum, suggesting that the effect of BCG vaccination on TST positivity may be more prolonged than typically expected (28). In addition, potentially confounding our results, children who received TSTs before and after immigration may have had immunologic boosting, resulting in falsely positive TSTs and IGRAs (29).
Region of origin was a notable risk factor for positive TB test results. Children from Southeast Asia had greater odds of having a positive result for TST, IGRA, or both than did children from eastern Mediterranean countries and the Americas, but we found no difference for these children compared with those from Africa. This finding is consistent with known epidemiologic risk factors: the prevalence of TB disease is high in countries in Africa and Southeast Asia, and Southeast Asia has a higher prevalence of TB disease than eastern Mediterranean countries and Cuba (where most children from the Americas region originated) (30).
Age was another noteworthy risk factor for positive TB test results. Children <2 years and >14 years of age had a higher prevalence of positive results for TST, IGRA, or both compared with children 2–14 years of age. Older children (>14 years of age) in our cohort had increased prevalence of positive TB test results by both the TST and IGRA, which more likely represented true TB infection because of the children’s greater time outside the home and cumulative exposure to adults with infectious pulmonary TB (30–34). The higher frequency of positive tests in children <2 years of age, on the other hand, is more difficult to explain. Higher TST positivity in children <2 years of age likely represented greater cross-reactivity with BCG, given the temporal proximity to vaccination or potential boosting if children had serial TSTs performed (before and after immigration). However, BCG immunization cannot explain the increased prevalence of positive IGRA results in these young children. Furthermore, these data contradict previous studies that demonstrate that older children are more likely to have TB infection (30–34). One possible explanation is that IGRA-positive children <2 years of age in our cohort had more prolonged exposure to an adult family member with infectious pulmonary TB in the home, because very young children spend more time in the home than their school-aged counterparts. To date, IGRAs have not been used routinely for the diagnosis of TB infection in children <2 years of age because of a paucity of data on test performance (35).
Most previous estimates of the prevalence of TB infection in immigrant children used the TST as the test of choice, given an initial paucity of pediatric data and the scarcity and cost of IGRAs. Our findings paralleled the results of a recent study using IGRA testing, which estimated that 5.6% of immigrant children had TB infection, compared with previous estimates of 22% based on TST testing (36). American Academy of Pediatrics guidelines currently recommend IGRA use down to 2 years of age (35); some experts recommend using IGRAs in children as young as 1 year of age. Use of IGRAs rather than the TST would likely reduce false positive tests and allow for TB infection therapy to be targeted to those who would most benefit.
The CDC does not recommend tiered testing (that is, obtaining an IGRA if a TST result is positive) for TB infection. However, at times, the initial test of infection, selected either by choice or by necessity, is not the optimal test, particularly for a BCG-immunized child. In our study, all children had greater odds of having a positive TST result compared with a positive IGRA test regardless of immigration classification, region of origin, or age. In addition, we had almost 300 children in whom both TSTs and IGRAs were obtained, of whom 20% had discordant results, mostly TST+/IGRA–. Our findings are consistent with a prior study that demonstrated that for BCG-immunized children who have immigration-related testing, false positive TST results are common, and IGRAs should be the tests of choice for this patient population (10).
Discordance between TST and IGRA results was seen in all age groups. Although false-positive results are an expected limitation of TST use among BCG-vaccinated children, the impact of BCG vaccine in causing falsely positive TST results has typically been thought to be temporally related to BCG vaccine receipt, which in most countries is a single dose immediately after birth. However, discordant TST and IGRA results in older children suggest either that the effect of some strains of BCG on the TST result lasts longer than previously recognized (28) or that the effect of nontuberculous mycobacteria infections that also can cause a falsely positive TST result may be underestimated in children from developing nations. A third possibility is that immunologic boosting as a result of repeat skin testing before and after immigration may have resulted in false positive TSTs (29). Concerns about false positive TST results are considered in updated 2018 guidelines (9) for TB testing before immigration, thereby suggesting use of IGRAs for all persons >2 years of age.
Our study has limitations. Although we have follow-up data from the Texas Children’s Hospital TB clinic for most children evaluated for a positive test of TB infection, we do not have data for some children evaluated at other clinics or for children whose test for TB infection was negative. BCG vaccination status was not routinely documented; thus, the presumption of false-positive TSTs secondary to cross-reactivity with BCG assumes that most children were BCG-immunized. We assumed BCG vaccination because this vaccination is recommended in the national immunization programs of 95% of countries from which these children emigrated (37). HIV infection was rare in our cohort, precluding drawing meaningful conclusions regarding positive results for TST, IGRA, or both in HIV-infected children from our data. Finally, these data may not be generalizable to all immigrant children relocating to the United States because this study included predominantly children from TB high-burden countries (9).
In summary, the prevalence of positive TB test results in this cohort of children was lower than previously reported, and TB disease was rare. The lower prevalence of positive tests of TB infection in this childhood population likely stems from the predominant use of IGRA testing. The TST and IGRA results are frequently discrepant, particularly among those with lower-risk immigration classification, younger children who have received a BCG vaccine, and those from lower-burden countries.
As a result of these data and our experience, we advocate for other health jurisdictions to implement the routine use of IGRA testing for all children, regardless of immigration classification, region of origin, or age, who are evaluated as part of the immigration process to the United States. We also advocate for use of confirmatory IGRA testing in BCG-immunized children with no known TB contacts who have positive TST results. Use of IGRA as opposed to TST in BCG-immunized children would reduce false-positive test results and enable TB infection therapy to be targeted to those who would most benefit.
Dr. Lamb is an assistant in medicine at Boston Children’s Hospital and a Clinical Instructor at Harvard Medical School, Boston, Massachusetts, USA. Her research interests are in Mycobacteria and epidemiology.
Acknowledgment
We thank our colleagues in the Harris County Public Health Refugee Health Screening Program, City of Houston Tuberculosis Program, and the US Committee for Refugees and Immigrants for their collaboration in caring for our children.
References
- World Health Organization. Global TB report 2018 [cited 2019 Feb 25]. https://apps.who.int/iris/bitstream/handle/10665/274453/9789241565646-eng.pdf
- Dodd PJ, Gardiner E, Coghlan R, Seddon JA. Burden of childhood tuberculosis in 22 high-burden countries: a mathematical modelling study. Lancet Glob Health. 2014;2:e453–9. DOIPubMedGoogle Scholar
- De Bruijn B. The living conditions and well-being of refugees. United Nations Development Program, New York City 2018 [cited 2019 Feb 25]. http://hdr.undp.org/sites/default/files/hdrp_2009_25.pdf
- US Citizenship and Immigration Services. Special immigrants [cited 2019 Feb 25]. https://www.uscis.gov/humanitarian/special-immigrants
- Coburn N, Sharan T. Out of harm’s way? Perspectives of the special immigrant visa program for Afghanistan, July 2016 [cited 2019 Feb 25]. http://www.hollingscenter.org/wp-content/uploads/2016/09/SIV-Full-Report.pdf
- World Health Organization. Tuberculosis country profiles: Cuba [cited 2019 Feb 25]. https://extranet.who.int/sree/Reports?op=Replet&name=%2FWHO_HQ_Reports%2FG2%2FPROD%2FEXT%2FTBCountryProfile&ISO2=CU&LAN=EN&outtype=html
- Wasem RE. Immigration policy on Haitian migrants. Congressional Research Service, May 17, 2011 [cited 2019 Feb 25]. https://fas.org/sgp/crs/row/RS21349.pdf
- Krogstad JM. Surge in Cuban immigration to U.S. continued through 2016. Pew Research Center, January 13, 2017 [cited 2019 Feb 25]. http://www.pewresearch.org/fact-tank/2017/01/13/cuban-immigration-to-u-s-surges-as-relations-warm
- Centers for Disease Control and Prevention. Tuberculosis technical instructions for panel physicians; 2018 [cited 2019 Mar 14]. https://www.cdc.gov/immigrantrefugeehealth/exams/ti/panel/tuberculosis-panel-technical-instructions.html?CDC_AA_refVal=https%3A%2F%2Fwww.cdc.gov%2Fimmigrantrefugeehealth%2Fexams%2Fti%2Fpanel%2Ftuberculosis-implementation.html
- Taylor EM, Painter J, Posey DL, Zhou W, Shetty S. Latent tuberculosis infection among immigrant and refugee children arriving in the United States: 2010. J Immigr Minor Health. 2016;18:966–70. DOIPubMedGoogle Scholar
- Hayes EB, Talbot SB, Matheson ES, Pressler HM, Hanna AB, McCarthy CA. Health status of pediatric refugees in Portland, ME. Arch Pediatr Adolesc Med. 1998;152:564–8. DOIPubMedGoogle Scholar
- Geltman PL, Radin M, Zhang Z, Cochran J, Meyers AF. Growth status and related medical conditions among refugee children in Massachusetts, 1995-1998. Am J Public Health. 2001;91:1800–5. DOIPubMedGoogle Scholar
- Sheikh M, Pal A, Wang S, MacIntyre CR, Wood NJ, Isaacs D, et al. The epidemiology of health conditions of newly arrived refugee children: a review of patients attending a specialist health clinic in Sydney. J Paediatr Child Health. 2009;45:509–13. DOIPubMedGoogle Scholar
- Gray K, Wood N, Gunasekera H, Sheikh M, Hazelton B, Barzi F, et al. Vitamin d and tuberculosis status in refugee children. Pediatr Infect Dis J. 2012;31:521–3. DOIPubMedGoogle Scholar
- Lucas M, Nicol P, McKinnon E, Whidborne R, Lucas A, Thambiran A, et al. A prospective large-scale study of methods for the detection of latent Mycobacterium tuberculosis infection in refugee children. Thorax. 2010;65:442–8. DOIPubMedGoogle Scholar
- US Department of State Bureau of Population, Refugees, and Migration. Refugee Processing Center; 2018 [cited 2019 Feb 25]. http://ireports.wrapsnet.org
- Busch-Armendariz N, Nale NL, Kamerr-Kerwick M, Kellison JB, Torres MIM, Cook-Heffron L, et al. Human trafficking by the numbers: the initial benchmark of prevalence and economic impact for Texas. The University of Texas at Austin, School of Social Work, Institute on Domestic Violence and Sexual Assault; 2016 [cited 2019 Feb 25]. https://repositories.lib.utexas.edu/bitstream/handle/2152/44597/idvsa-2016-human-trafficking-by-the-numbers.pdf
- US Citizenship and Immigration Services. Refugees [cited 2019 Mar 18]. https://www.uscis.gov/humanitarian/refugees-asylum/refugees
- US Citizenship and Immigration Services. Asylum [cited 2019 Mar 18]. https://www.uscis.gov/humanitarian/refugees-asylum/asylum
- US Citizenship and Immigration Services. The Cuban family reunification parole program [cited 2019 Mar 18]. https://www.uscis.gov/humanitarian/humanitarian-parole/cuban-family-reunification-parole-program
- US Department of State – Bureau of Consular Affairs. Special immigrant visas (SIVs) for Iraqi and Afghan translators/interpreters [cited 2019 Mar 18]. https://travel.state.gov/content/travel/en/us-visas/immigrate/siv-iraqi-afghan-translators-interpreters.html
- National Human Trafficking Hotline. Federal law [cited 2019 Mar 25]. https://humantraffickinghotline.org/what-human-trafficking/federal-law
- World Health Organization Member States. Regional offices [cited 2019 Feb 25] https://www.who.int/about/regions/en
- Mazurek GH, Jereb J, Vernon A, LoBue P, Goldberg S, Castro K; IGRA Expert Committee; Centers for Disease Control and Prevention (CDC). Updated guidelines for using Interferon Gamma Release Assays to detect Mycobacterium tuberculosis infection - United States, 2010. MMWR Recomm Rep. 2010;59(RR-5):1–25.PubMedGoogle Scholar
- Lewinsohn DM, Leonard MK, LoBue PA, Cohn DL, Daley CL, Desmond E, et al. Official American Thoracic Society/Infectious Diseases Society of America/Centers for Disease Control and Prevention clinical practice guidelines: diagnosis of tuberculosis in adults and children. Clin Infect Dis. 2017;64:e1–33. DOIPubMedGoogle Scholar
- Graham SM, Cuevas LE, Jean-Philippe P, Browning R, Casenghi M, Detjen AK, et al. Clinical case definitions for classification of intrathoracic tuberculosis in children: an update. Clin Infect Dis. 2015;61(Suppl 3):S179–87. DOIPubMedGoogle Scholar
- Centers for Disease Control and Prevention. Tuberculosis—United States, 2018. MMWR. 2019 [cited 2019 May 10]. https://www.cdc.gov/mmwr/volumes/68/wr/mm6811a2.htm
- Seddon JA, Paton J, Nademi Z, Keane D, Williams B, Williams A, et al. The impact of BCG vaccination on tuberculin skin test responses in children is age dependent: evidence to be considered when screening children for tuberculosis infection. Thorax. 2016;71:932–9. DOIPubMedGoogle Scholar
- van Zyl-Smit RN, Zwerling A, Dheda K, Pai M. Within-subject variability of interferon-g assay results for tuberculosis and boosting effect of tuberculin skin testing: a systematic review. PLoS One. 2009;4:
e8517 . DOIPubMedGoogle Scholar - World Health Organization. Tuberculosis country profile [cited 2019 Feb 25]. https://www.who.int/tb/country/data/profiles/en/
- Pediatric Tuberculosis Collaborative Group. Targeted tuberculin skin testing and treatment of latent tuberculosis infection in children and adolescents. Pediatrics. 2004;114(s4):1175–201. DOIGoogle Scholar
- Seddon JA, Shingadia D. Epidemiology and disease burden of tuberculosis in children: a global perspective. Infect Drug Resist. 2014;7:153–65.PubMedGoogle Scholar
- Young J, O’Connor ME. Risk factors associated with latent tuberculosis infection in Mexican American children. Pediatrics. 2005;115:e647–53. DOIPubMedGoogle Scholar
- Gounder CR, Driver CR, Scholten JN, Shen H, Munsiff SS. Tuberculin testing and risk of tuberculosis infection among New York City schoolchildren. Pediatrics. 2003;111:e309–15. DOIPubMedGoogle Scholar
- American Academy of Pediatrics Committee on Infectious Diseases. Red Book: report of the Committee on Infectious Diseases. Elk Grove Village (IL): American Academy of Pediatrics; 2018.
- Howley MM, Painter JA, Katz DJ, Graviss EA, Reves R, Beavers SF, et al.; Tuberculosis Epidemiologic Studies Consortium. Evaluation of QuantiFERON-TB gold in-tube and tuberculin skin tests among immigrant children being screened for latent tuberculosis infection. Pediatr Infect Dis J. 2015;34:35–9. DOIPubMedGoogle Scholar
- The BCG World Atlas 2nd Edition [cited 2019 Mar 14]. http://www.bcgatlas.org
Figures
Tables
Follow Up
Earning CME Credit
To obtain credit, you should first read the journal article. After reading the article, you should be able to answer the following, related, multiple-choice questions. To complete the questions (with a minimum 75% passing score) and earn continuing medical education (CME) credit, please go to http://www.medscape.org/journal/eid. Credit cannot be obtained for tests completed on paper, although you may use the worksheet below to keep a record of your answers.
You must be a registered user on http://www.medscape.org. If you are not registered on http://www.medscape.org, please click on the “Register” link on the right hand side of the website.
Only one answer is correct for each question. Once you successfully answer all post-test questions, you will be able to view and/or print your certificate. For questions regarding this activity, contact the accredited provider, CME@medscape.net. For technical assistance, contact CME@medscape.net. American Medical Association’s Physician’s Recognition Award (AMA PRA) credits are accepted in the US as evidence of participation in CME activities. For further information on this award, please go to https://www.ama-assn.org. The AMA has determined that physicians not licensed in the US who participate in this CME activity are eligible for AMA PRA Category 1 Credits™. Through agreements that the AMA has made with agencies in some countries, AMA PRA credit may be acceptable as evidence of participation in CME activities. If you are not licensed in the US, please complete the questions online, print the AMA PRA CME credit certificate, and present it to your national medical association for review.
Article Title:
Tuberculosis in Internationally Displaced Children Resettling in Harris County, Texas, USA, 2010–2015
CME Questions
1. You are seeing a 13-year-old girl who recently emigrated from Afghanistan for a well-child check. What does the Centers for Disease Control and Prevention (CDC) recommend regarding tuberculosis (TB) screening for this patient?
A. No screening is needed without symptoms or known TB exposures
B. Only an interferon-gamma release assay (IGRA) is required
C. Only a tuberculin skin test (TST) is required
D. A TST should be applied, and a positive test should be confirmed with an IGRA
2. The patient's mother reports that she had a positive TST at the US consulate 4 months ago, before departing Afghanistan. What was the approximate rate of discrepant test results between TSTs and IGRAs in the current study?
A. 20%
B. 30%
C. 40%
D. 60%
3. What can you tell this family about the results of TB testing in the current study?
A. The rate of any positive TB test was 22%
B. Only 40% of children with a positive TB test were ultimately diagnosed with TB infection
C. About 1% of children were diagnosed with TB disease
D. 10% of children with TST-positive/IGRA-negative testing eventually developed TB disease
4. Which one of the following variables was most associated with a higher TST or IGRA in the current study?
A. Immigration classification
B. Female sex
C. Age between 2 and 13 years of age
D. Immigration from Southeast Asia vs other regions
Original Publication Date: July 17, 2020
1Preliminary results from this study were presented at the North American Union TB Conference, February 28–March 3, 2018, Chicago, IL, USA.
2Current affiliation: Harvard Medical School, Boston, Massachusetts, USA.
Related Links
Table of Contents – Volume 26, Number 8—August 2020
EID Search Options |
---|
Advanced Article Search – Search articles by author and/or keyword. |
Articles by Country Search – Search articles by the topic country. |
Article Type Search – Search articles by article type and issue. |
Please use the form below to submit correspondence to the authors or contact them at the following address:
Gabriella Lamb, Harvard Medical School, 333 Longwood Ave, Boston, MA 02115, USA
Top