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Childhood TB epidemiology and treatment outcomes in Thailand: a TB active surveillance network, 2004 to 2006
© Lolekha et al; licensee BioMed Central Ltd. 2008
Received: 26 December 2007
Accepted: 18 July 2008
Published: 18 July 2008
Of the 9.2 million new TB cases occurring each year, about 10% are in children. Because childhood TB is usually non-infectious and non-fatal, national programs do not prioritize childhood TB diagnosis and treatment. We reviewed data from a demonstration project to learn more about the epidemiology of childhood TB in Thailand.
In four Thai provinces and one national hospital, we contacted healthcare facilities monthly to record data about persons diagnosed with TB, assist with patient care, provide HIV counseling and testing, and obtain sputum for culture and susceptibility testing. We analyzed clinical and treatment outcome data for patients age < 15 years old registered in 2005 and 2006.
Only 279 (2%) of 14,487 total cases occurred in children. The median age of children was 8 years (range: 4 months, 14 years). Of 197 children with pulmonary TB, 63 (32%) were bacteriologically-confirmed: 56 (28%) were smear-positive and 7 (4%) were smear-negative, but culture-positive. One was diagnosed with multi-drug resistant TB. HIV infection was documented in 75 (27%). Thirteen (17%) of 75 HIV-infected children died during TB treatment compared with 4 (2%) of 204 not known to be HIV-infected (p < 0.01).
Childhood TB is infrequently diagnosed in Thailand. Understanding whether this is due to absence of disease or diagnostic effort requires further research. HIV contributes substantially to the childhood TB burden in Thailand and is associated with high mortality.
TB causes 9.2 million illnesses and 1.7 million deaths annually . About 10% of these TB cases occur in children, i.e., persons less than 15 years old [2–4]. In most countries, national TB programs (NTPs) focus case finding and treatment on pulmonary, acid-fast bacilli (AFB) smear-positive cases, which can be rapidly and reliably diagnosed and contribute greatest to community TB transmission . Because most childhood TB cases are not smear-positive, children are given lower priority in NTPs. Historically, TB surveillance systems in high-burden countries only recorded age categories for smear-positive cases; as a result, few NTPs have been able to report reliably the total number of childhood TB cases diagnosed and treated annually . The World Health Organization (WHO) recommends TB disease screening in children who live in the household of a smear-positive case, but few NTPs perform this routinely .
Despite the lack of attention paid by NTPs, childhood TB is an important public health problem. Because most children have primary, rather than reactivation, disease, childhood TB is considered a "sentinel" event, indicating recent TB transmission, often from an infectious, undiagnosed TB case in the same household . Identifying and treating TB infection and disease in children can also provide long-term benefits to TB control, preventing future cases due to reactivation . The global HIV pandemic has accelerated the urgency of TB control in children. Rates of childhood TB appear to be rising, particularly in countries with generalized HIV epidemics . Multiple studies from sub-Saharan Africa have documented a markedly increased mortality rate for HIV-infected children with TB compared to HIV-uninfected children with TB or to HIV-infected children without TB [8–12].
WHO has recently called for more studies to define the global epidemiology of childhood TB, because the literature remains scant, dominated primarily by studies from industrialized countries and South Africa . Few epidemiologic studies of pediatric TB have been published from Asia. Thailand is among the 22 high-burden TB countries on WHO's list and has a generalized HIV epidemic . Notification rates for childhood TB in Thailand are markedly lower than in other countries; in fact, the proportion of all reported TB cases that occur in children (2.7%) is the lowest of the 22 high-burden countries . We analyzed data from a multi-province demonstration project to understand characteristics, treatment outcomes, and risk factors for death and default in childhood TB cases.
The Thailand TB Active Surveillance Network is a demonstration project, implemented by the Thailand Ministry of Public Health (MOPH), Bangkok Metropolitan Administration (BMA), U.S. Centers for Disease Control and Prevention (CDC), and Research Institute of Tuberculosis, Japan (RIT), involving all districts in three provinces (Chiang Rai, Phuket, Ubon-ratchathani), selected districts in Bangkok (2 in 2005; 9 in 2006), and one national infectious diseases hospital (Bamrasnaradura Institute). In 2006, the catchment area included 59 public and 26 private healthcare facilities. In 2005, the last year for which published population estimates were available, the estimated number of persons aged 0 – 14 years old in the catchment area was 743,574, including 218,012 aged 0–4 years and 525,562 aged 5–14 years; for this calculation, we excluded the national infectious diseases hospital because this referral facility has no definable catchment area (unpublished data, Thailand National Statistics Department and BMA Office). A detailed description of this project, including methods, has been published elsewhere .
Thai national guidelines recommend that childhood pulmonary TB (PTB) be diagnosed using a combination of factors, including: history of contact with a PTB patient known to be sputum smear-positive for acid-fast bacilli (AFB); suspected TB symptoms and signs; an abnormal chest radiograph, including pulmonary infiltrates and/or hilar or mediastinal lymphadenopathy; sputum or gastric aspirates that are smear-positive; and tuberculin skin testing. Because this project relied on data collected as part of routine TB control and most cases occurred in adults, limited information was collected about diagnostic tests other than chest radiography, sputum microscopy, and sputum culture. We did not collect data about tuberculin skin testing. Gastric aspirate specimens were classified as sputum specimens, in accordance with the routine TB program practice of classifying patients with abnormal chest radiographs and AFB-positive gastric aspirates as having smear-positive, pulmonary TB. In Thailand, criteria for EPTB diagnosis are less clearly delineated.
All public hospitals are able to process sputum for AFB smear microscopy. As part of this demonstration project, physicians were encouraged to send sputum specimens for mycobacterial culture at a province-level facility. All specimens were initially cultured on solid media, either Lowenstein-Jensen (LJ) or Ogawa medium, and, during mid-2005, additionally on liquid media with an automated reading instrument (Mycobacterial Growth Indicator Tube [MGIT]; BACTEC 960, Becton-Dickinson Corporation). Isolates underwent drug-susceptibility testing (DST) against first-line drugs (streptomycin, isoniazid, rifampin, pyrazinamide, ethambutol) at the Bangkok municipal or national TB reference laboratories.
A case of childhood TB was defined as a person aged 0 – 14 years old who was diagnosed with TB and treated for TB disease. A "new" case of TB was considered TB disease in a person who reported no or less than 1 month of previous TB treatment.
Thai national guidelines recommend standardized, internationally-accepted treatment regimens for children. Treatment outcomes were defined using standard WHO categories .
HIV diagnosis and treatment
In this demonstration project, nurses and physicians from public and private healthcare facilities were trained in HIV counseling and testing. They were encouraged to provide HIV counseling and testing to TB patients and referrals to HIV-related care and treatment to HIV-infected TB patients. No financial incentives were provided to patients or healthcare workers for HIV testing. Individual physicians used their own judgment about whether to measure CD4+ T-cell lymphocyte counts (CD4), provide opportunistic infection (OI) prophylaxis or anti-retroviral therapy (ART), and manage other clinical conditions. When performed, blood for CD4 counts was usually drawn during the first month of TB treatment.
Data collection and analysis
Data were collected on standardized forms that include questions about demographics, clinical history, laboratory and radiographic testing, TB treatment regimens, TB treatment outcomes, and HIV-related information (infection status, CD4, use of OI prophylaxis or ART). Data were analyzed using the Statistical Package for Social Sciences (SPSS) for Windows, version 12 software (SPSS Inc., Chicago, IL, USA) for analysis. Rates of childhood TB (per 100,000) were determined from surveillance data and population estimates; when calculating rates, we excluded reports from the national infectious diseases hospital, which has no population denominator. We classified age as 0–4 and 5–14 consistent with international recommendations . Differences between groups were compared with X2 test for categorical variables within different age groupings; where appropriate, Fisher's exact test was used. Statistical significance was defined as p < 0.05. Factors significant in univariate analysis or factors likely to be associated with outcomes were included in multivariate models using logistic regression, and automated backward, stepwise logistic regression was used to construct final models. We calculated odds ratios (OR), adjusted OR (AOR) and 95% confidence intervals (CI).
The protocol for this demonstration project was reviewed by the Thailand MOPH and CDC and found to be surveillance and public health program implementation not requiring oversight by a human subjects research institutional review board.
Case finding and incidence
Characteristics of 279 childhood TB patients reported in the Thailand TB active surveillance network, October 2004 to September 2006
Patients No. (%)
Type, anatomic site of TB
Category of TB
Treatment after default
Median age (years) (range)
8 (4 months-14 years)
Age group (years)
Mobile within the past 6 months
Median number of persons living in home, persons (range)
Median number of additional children < 5 years old living in home, persons (range)
Previously treated for TB
Previously treated with isoniazid for latent TB infection
Cough lasting > 2 weeks at time of diagnosis
Living in migrant or refugee camp
Facility that made TB diagnosis
Government hospital or clinic
Facility that provided TB treatment
Government hospital or clinic
Presence of a cavity
Microbiological characteristics of pulmonary TB cases
Smear-positive and culture-positive
Smear-positive and culture-negative or culture not done
Smear-negative and culture-positive
Neither smear- nor culture-positive
Initial treatment prescribed
CAT I (2HRZE/4HR)
CAT II (2HRZES/1HRZ/4HR)
CAT III (2HRZ/4HR)
CAT IV (2HRZS/4HR)
Observer assigned during first 2 months of treatment
Health care or village health worker
Offered HIV counseling after diagnosis of TB
HIV status already known
Among pulmonary smear-positive patients, sputum converted to smear-negative after 2 months of treatment
Success (completed, cured)
Of 74 children aged 0–4, 8 (11%) had pulmonary, smear-positive TB, compared with 48 (23%) of 205 children aged 5–14 (p < 0.01). The proportion with EPTB and sites involved did not differ by age group.
Characteristics of cases
The median age was 8 years, and only 9 (3%) were younger than 1 year (Table 1). Half were male. Non-Thais, e.g., migrants, refugees, visitors, or other foreigners, accounted for 13% of cases. Only 2% of cases were diagnosed at a private facility. Previous treatment for TB disease was documented in 17 (6%) and for latent TB infection in 12 (4%). Almost half (43%) had cough lasting more than 2 weeks, and most (69%) had abnormal chest radiographs.
Of 197 pulmonary TB cases, 159 (81%) had at least one sputum smear performed, and 79 (50%) of these had at least one sputum culture performed. Of cases with a culture performed, 41 (52%) were culture-positive for Mycobacterium tuberculosis. Overall, 34 (17%) of the pulmonary TB cases were smear-positive and culture-positive, 22 (11%) were only smear-positive (4 culture-negative; 5 culture not done; 4 culture-positive for non-tuberculous mycobacterium [NTM]; and 9 culture unknown/missing), 134 (68%) were neither smear nor culture positive (24 culture-negative; 38 culture not done; 15 neither smear nor culture done; 57 culture unknown/missing), and 7 (4%) were smear-negative and culture-positive. Of 41 culture-positive cases, 33 (80%) had DST performed. MDR TB was diagnosed in 1, which was 0.5% of all 197 pulmonary TB cases and 3% of the 33 culture-positive cases that had DST performed.
Of 279 TB cases, 68 (24%) had known HIV status before their diagnosis of TB. Of the remaining 211 cases with unknown HIV status, 148 (53%) underwent HIV counseling; 108 (73%) of those counseled agreed to HIV testing. In all, 75 (27%) cases were known to be HIV-infected (55 or 73% of whom knew their HIV status before TB diagnosis), 102 (37%) were known to be HIV-uninfected, and 102 (37%) had unknown HIV status.
Of the 75 HIV-infected TB patients, 21 (28%) were pulmonary, smear-positive; 32 (43%) smear-negative; 7 (9%) smear not known or done and 15 (20%) extra-pulmonary. Most (77%) were new cases. Half were male, and 81% were more than 5 years old. CD4 counts were available for 46 (61%) cases. The median was 55 (range: 2; 2731) and mean 193 cells/mm3. The distribution of CD4 was similar in those 0–4 years old (in whom absolute CD4 is known to be unreliable) compared with those 5–14 years old. Only 6 (16%) of children aged 5–14 years had CD4 greater than 200 cells/mm3. ART was prescribed to 17 (23%) before the diagnosis of TB and to 16 (21%) during TB treatment. ART was not prescribed to 18 (24%) and was not known for 24 (32%). Of 32 HIV-infected children aged 5–14 years who had CD4 less than 200 cells/mm3, 20 (62%) received ART. Among children receiving ART, about half (45%) received a combination regimen of stavudine, lamivudine, and nevirapine. Rates of co-trimoxozole use were higher than ART; 23 (31%) were taking co-trimoxazole before their diagnosis of TB, and 21 (28%) were prescribed co-trimoxazole during TB treatment. Almost all (97%) children with CD4 less than 200 cell/mm3 received co-trimoxazole.
Treatment outcomes for childhood TB cases, stratified by age group and HIV status, in Thailand TB active surveillance network, October 2004 to September 2006
Treatment outcome No. (%) registered
Cured or completed
Treatment outcomes for childhood TB cases, categorized by anatomic site and/or microbiologic characteristics, in Thailand TB active surveillance network, October 2004 to September 2006
Treatment outcome No. (%) registered
Cured or completed
All types of TB
Neither smear nor culture Positive
Culture or smear positive
Smear positive only
Other types of ETB
Factors associated with death or default
Factors associated with death versus successful (cure or completed) outcome among childhood TB cases in Thailand, October 2004 to September 2006
No. died/total (%)
Unadjusted OR (95% CI)
Adjusted OR (95% OI)
Age (in years)
National infectious diseases hospital
Factors associated with default versus successful (cure or completed) outcome among childhood TB cases in Thailand, October 2004 to September 2006
No. defaulted/total (%)
Unadjusted OR (95% CI)
Adjusted OR (95% OI)
Age (in years)
National infectious diseases hospital
We found that childhood TB is infrequently diagnosed in Thailand. In our population, the rate of childhood TB was 14 cases per 100,000, consistent with one published estimate, derived from the WHO global report, of childhood TB incidence in Thailand (15 cases per 100,000 children) . The rate of smear-positive TB in our population was much higher (3 per 100,000 versus 1 per 100,000) than routine national surveillance data. There are at least two possible explanations for the higher case detection rate in our project compared with national surveillance. First, national surveillance may not sufficiently capture all diagnosed cases of TB. Our demonstration project involved contacting healthcare facilities regularly to ascertain diagnosed cases of TB; it is likely that we identified cases of TB that would not normally have been reported . Second, and conversely, our surveillance sites may over-estimate the overall burden of childhood TB in Thailand, because the participating provinces have higher TB and HIV prevalence rates than the national average and have enhanced TB laboratory capacity. Enhancing the national surveillance system to collect age data for all forms of TB, to differentiate between children aged 0–4 and 5–14, to collect microbiological characteristics of pulmonary TB cases, and to integrate HIV-related data would permit more detailed analysis and better define the burden of childhood TB in Thailand. We found a low rate of extra-pulmonary TB compared to other reports . It is possible that high coverage of BCG vaccination can prevent invasive TB disease. We did not collect data on history of BCG vaccination or BCG scar; however, national coverage of BCG vaccine in 2006 was more than 99% .
Unfortunately, measuring the true burden of childhood TB in any country is extremely difficult, because no diagnostic test performs well in childhood TB. Most children cannot expectorate sputum and/or have pauci-bacillary pulmonary TB. Gastric aspiration and sputum induction, although validated, are used mainly in academic or big referral hospitals and are infrequently used in small hospitals because of technical demands and relatively low yield . In our project, most cases were not bacteriologically-confirmed, consistent with data from both low- and high-burden TB countries . International guidelines also instruct clinicians to use radiographic changes, tuberculin skin testing, symptoms, and contact with a known TB case as clues to the diagnosis . Our enhanced surveillance system did not record sufficient detail about these characteristics and gastric aspiration to allow us to assess the accuracy of TB diagnosis. Further, because contact investigations are rarely performed in Thailand, many childhood TB cases may have gone undiagnosed in the community. A more detailed evaluation of clinical diagnostic and public health practices in Thailand is needed to understand the accuracy of childhood TB diagnosis and the relative contribution of diagnostic effort to differences in reporting rates.
HIV contributes substantially to the burden of childhood TB in Thailand. The minimum prevalence of HIV infection in children (27%) was similar to that in adults (31%) recorded in our surveillance system (Thailand MOPH, unpublished data). The HIV prevalence was higher in older children than in younger children, likely because of the effectiveness of Thailand's highly effective mother-to-child HIV transmission that began in 2000 . Almost one-fifth of HIV-infected children with TB died during TB treatment, all of them aged 5–14. The markedly advanced immune-suppression in these children is identical to that seen in HIV-infected Thai adults, in whom TB occurs almost exclusively at low CD4 levels [14, 18]. Our data shows that despite national TB and HIV treatment guidelines, coverage of some key aspects of TB and HIV care was low. As in adults, reducing TB morbidity and mortality in HIV-infected children requires further integration of HIV counseling and testing into TB services, ART and co-trimoxazole for HIV-infected TB patients, prevention of TB through treatment of latent TB infection, and earlier diagnosis through contact investigations and routine screening for TB disease in HIV-infected children. Documenting CD4 percentage, as well as absolute count, on TB registers will assist in identifying when children aged less than 5 years should be receiving ART as well as TB treatment.
Data on childhood TB treatment outcomes is scarce. One surprising finding was the high rate of default particularly patients with meningitis. Most defaults occurred in non-Thais, a heterogeneous group of 2.3 million people that consist of economic migrants, refugees, visitors, and other temporary residents . Because rates of default are known to be high in adult migrants with TB, our finding is worrisome, albeit expected. Further efforts are needed to maintain non-Thai adults and children on TB treatment to prevent drug resistance.
Our study has important limitations, particularly its small sample size and the absence of microbiologic confirmation in most diagnosed patients. Its primary strength is that it is the only population-based study that we know of about childhood TB epidemiology and treatment outcomes in Asia, a region that contributes to one-half of the global TB burden. Our data confirm that the burden of diagnosed childhood TB in Thailand is less than that in other high-burden countries, but it is substantially greater than national surveillance data indicate and is closely associated with the HIV epidemic. Strengthening national surveillance to capture all diagnosed cases of TB in children, providing training or guidance to health care providers in community hospitals how to perform gastric aspiration and to record more detailed data about childhood TB cases will help provide more accurate estimates of the national disease burden and potentially increase political commitment to address childhood TB. Reducing morbidity and mortality from TB in Thai children will require enhancing laboratory capacity for microbiologic confirmation of disease, increasing TB screening in household contacts and HIV-infected children, strengthening linkages to HIV-related services, and reducing default rates.
Childhood TB is infrequently diagnosed in Thailand. Understanding whether this is due to absence of disease or diagnostic effort requires further research. Strengthening national surveillance to capture all diagnosed cases of TB in children will help provide more accurate estimates of the national disease burden and potentially increase political commitment to address childhood TB. HIV contributes substantially to the childhood TB burden in Thailand and is associated with high mortality. Reducing morbidity and mortality from TB in Thai children will require enhancing laboratory capacity for microbiologic confirmation of disease, increasing TB screening in household contacts, reducing default rates and strengthening linkages to HIV-related services for HIV-infected children.
We express our gratitude to all health care providers and staff in the active TB surveillance network in Bangkok Metropolitan Administration, Chiang Rai province, Ubol-ratchathani province, Phuket province and Bamrasnaradura Institute for their support in making this project possible. This work was funded by the Thailand Ministry of Public Health, the U.S. Centers for Disease Control and Prevention, and the Research Institute of Tuberculosis (Japan) and the U.S. Agency for International Development.
- World Health Organization: Global tuberculosis control: surveillance, planning, financing. WHO report 2008. 2008, Geneva, Switzerland: World Health Organization, (WHO/HTM/TB/2008.393)Google Scholar
- Corbett EL, Watt CJ, Walker N, Maher D, Williams BG, Raviglione MC, Dye C: The growing burden of tuberculosis: global trends and interactions with the HIV epidemic. Arch Intern Med. 2003, 163: 1009-21. 10.1001/archinte.163.9.1009.View ArticlePubMedGoogle Scholar
- Nelson LJ, Wells CD: Global epidemiology of childhood tuberculosis. Int J Tuberc Lung Dis. 2004, 8: 636-47.PubMedGoogle Scholar
- World Health Organization: Treatment of tuberculosis: guidelines for national programmes. Geneva, Switzerland: WHO. 2003, (WHO/CDS/TB/2003.313)., 3Google Scholar
- Dye C, Watt CJ, Bleed DM, Hosseini SM, Raviglione MC: Evolution of tuberculosis control and prospects for reducing tuberculosis incidence, prevalence, and deaths globally. JAMA. 2005, 293: 2767-75. 10.1001/jama.293.22.2767.View ArticlePubMedGoogle Scholar
- Starke J: Childhood tuberculosis: ending the neglect. Int J Tuberc Lung Dis. 2002, 6: 373-4.PubMedGoogle Scholar
- World Health Organization: Guidance for national tuberculosis programmes on the management of tuberculosis in children. Geneva, Switzerland: WHO. 2006, (WHO/HTM/TB/2006.371)Google Scholar
- Palme IB, Gudetta B, Bruchfeld J, Muhe L, Giesecke J: Impact of human immunodeficiency virus 1 infection on clinical presentation, treatment outcome and survival in a cohort of Ethiopian children with tuberculosis. Pediatr Infect Dis J. 2002, 21: 1053-1061. 10.1097/00006454-200211000-00016.View ArticlePubMedGoogle Scholar
- Jeena PM, Pillay P, Pillay T, Coovadia HM: Impact of HIV-1 co-infection on presentation and hospital-related mortality in children with culture proven pulmonary tuberculosis in Durban, South Africa. Int J Tuberc Lung Dis. 2002, 6: 672-678.PubMedGoogle Scholar
- Mukadi YD, Wiktor SZ, Coulibaly IM, Coulibaly D, Mbengue A, Folquet AM, Ackah A, Sassan-Morokro M, Bonnard D, Maurice C, Nolan C, Kreiss JK, Greenberg AE: Impact of HIV infection on the development, clinical presentation, and outcome of tuberculosis among children in Abidjan, Cote d'Ivoire. AIDS. 1997, 11: 1151-1158. 10.1097/00002030-199709000-00011.View ArticlePubMedGoogle Scholar
- Chintu C, Mudenda V, Lucas S, Nunn A, Lishimpi K, Maswahu D, Kasolo F, Mwaba P, Bhat G, Terunuma H, Zumla A, UNZA-UCLMS Project Paediatric Post-mortem Study Group: Lung diseases at necropsy in African children dying from respiratory illnesses: a descriptive necropsy study. Lancet. 2002, 360: 985-90. 10.1016/S0140-6736(02)11082-8.View ArticlePubMedGoogle Scholar
- Blusse van Oud-Alblas HJ, van Vliet ME, Kimpen JL, de Villiers GS, Schaaf HS, Donald PR: Human immunodeficiency virus infection in children hospitalised with tuberculosis. Ann Trop Paediatr. 2002, 22: 15-23. 10.1179/027249302125000832.View ArticleGoogle Scholar
- World Health Organization: A research agenda for childhood tuberculosis: improving the management of childhood tuberculosis within national tuberculosis programmes: research priorities based on a literature review. Geneva, Switzerland: WHO. 2007Google Scholar
- Varma JK, Wiriyakitjar D, Nateniyom S, Anuwatnonthakate A, Monkongdee P, Sumnapan S, Akksilp S, Sattayawuthipong W, Charunsuntonsri P, Rienthong S, Yamada N, Akarasewi P, Wells CD, Tappero JW: Evaluating the potential impact of the new Global Plan to Stop TB: Thailand, 2004–2005. Bull WHO. 2007, 85: 586-92.PubMedPubMed CentralGoogle Scholar
- World Health Organization: WHO vaccine-preventable diseases monitoring system 2007 global summary – country profile Thailand. Geneva, Switzerland: WHO. 2007Google Scholar
- Zar HJ, Hanslo D, Apolles P, Swingler G, Hussey G: Induced sputum versus gastric lavage for microbiological confirmation of pulmonary tuberculosis in infants and young children: a prospective study. Lancet. 2005, 365: 130-4. 10.1016/S0140-6736(05)17702-2.View ArticlePubMedGoogle Scholar
- Plipat T, Naiwatanakul T, Rattanasuporn N, Sangwanloy O, Amornwichet P, Teeraratkul A, Ungchusak K, Mock P, Levine W, McConnell MS, Simonds R, Culnane M: Reduction in mother-to-child transmission of HIV in Thailand, 2001–2003: Results from population-based surveillance in six provinces. AIDS. 2007, 21: 145-51. 10.1097/QAD.0b013e328010e02d.View ArticlePubMedGoogle Scholar
- Akksilp S, Karnkawinpong , Wattanaamornkiat W, Viriyakitja D, Monkongdee P, Sitti W, Rienthong D, Siraprapasiri T, Wells CD, Tappero JW, Varma JK: Antiretroviral therapy during tuberculosis treatment and marked reduction in death rate of HIV-infected patients, Thailand. Emerg Infect Dis. 2007, 13 (7): 1001-7.View ArticlePubMedPubMed CentralGoogle Scholar
- Huguet JW, Punpuing S: International migration in Thailand. International Organization for Migration, Regional Office, Bangkok, Thailand. 2005, [http://www.old.iom.int/documents/publication/international_migration_thailand_23_aug_05.pdf]Google Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/8/94/prepub
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