Skip to main content
Public Health Action logoLink to Public Health Action
. 2013 Mar 21;3(1):15–19. doi: 10.5588/pha.12.0055

The burden and outcomes of childhood tuberculosis in Cotonou, Benin

S Ade 1,, A D Harries 2,3, A Trébucq 2, S G Hinderaker 4, G Ade 1,, G Agodokpessi 1, D Affolabi 1, S Koumakpaï 5, S Anagonou 1, M Gninafon 1
PMCID: PMC4463074  PMID: 26392989

Abstract

Setting:

The National Tuberculosis Programme (NTP) and the paediatric ward of the General Hospital (GH), Cotonou, Benin.

Objective:

To describe the burden of tuberculosis (TB), characteristics and outcomes among children treated in Cotonou from 2009 to 2011.

Design:

Cross-sectional cohort study consisting of a retrospective record review of all children with TB aged <15 years.

Results:

From 2009 to 2011, 182 children with TB were diagnosed and treated (4.5% of total cases), 153 (84%) by the NTP and 29 (16%) by the GH; the latter were not notified to the NTP. The incidence rate of notified TB cases was between 8 and 13 per 100 000 population, and was higher in children aged >5 years. Of 167 children tested, 29% were HIV-positive. Treatment success was 72% overall, with success rates of 86%, 62% and 74%, respectively, among sputum smear-positive, sputum smear-negative and extra-pulmonary patients. Treatment success rates were lower in children with sputum smear-negative TB (62%) and those with HIV infection (58%).

Conclusion:

The number of children being treated for TB is low, and younger children in particular are underdiagnosed. There is a need to improve the diagnosis of childhood TB, especially among younger children, and to improve treatment outcomes among HIV-TB infected children, with better follow-up and monitoring.

Keywords: tuberculosis, children, NTP, general hospital, outcome


Globally, childhood tuberculosis (TB) has received limited priority in National TB Programmes (NTPs) due to the fact that children tend to be smear-negative and are therefore perceived to have limited infectiousness; also, numbers are often thought to be few.1 The numbers of children reported with TB may also be inaccurate due to difficulties in diagnosing both pulmonary and extra-pulmonary TB.

Children aged <15 years constitute about 11% of the estimated 9 million TB cases worldwide,2 and up to 15% in low-income countries.3 Although this proportion may seem small, TB in children aged <5 years, particularly those aged <2 years, has been shown to cause high mortality and morbidity.4 Globally, TB has been reported to be one of the most important causes of death among children,2 and treatment outcomes among children with TB have also been found to be poor.5

In Benin, information about the burden of TB in children is limited. While children with TB are registered and their outcomes are recorded in the NTP’s TB register, only sputum smear-positive pulmonary cases (grouped together into the 0–14 year age group) are specifically identified in the NTP’s quarterly reports. At the General Hospital (GH) in Cotonou, the economic capital, children are diagnosed and treated on the basis of information recorded in their personal medical files, but are never notified to the NTP, for a variety of reasons. NTP data on children are therefore incomplete and cannot be used to estimate the true burden of childhood disease in Benin.

The aim of the present study was to describe the burden of TB and characteristics and outcomes along children treated in Cotonou, Benin. Specific objectives were to determine: 1) the total number of TB cases recorded in the NTP TB registers, and of these, the number of children aged <15 years; 2) the incidence rate of notified TB cases among children aged <15 years; 3) the number of children notified with TB in the NTP TB register and the number of children recorded in the GH medical files (who are not notified in the NTP TB register) and, in each of these groups, stratification by sex, age, type of TB and human immunodeficiency virus (HIV) status; and 4) the treatment outcomes among these children stratified by place of treatment, sex, age, type of TB and HIV status, from 2009 to 2011.

STUDY POPULATION, DESIGN AND METHODS

Study design

This was a cross-sectional, retrospective cohort study of children with TB in Cotonou based on reviews of NTP TB registers and the medical files of the GH.

Setting

Benin is a small country in West Africa with a population of 9 million and a gross national income of US$780 per capita (http://data.worldbank.org/about/country-classifications). The NTP notifies about 3500 TB cases each year. The national incidence rate of notified new TB cases has been stable over the last 10 years, at 41–46 per 100 000 population. The NTP follows the DOTS strategy and uses internationally recognised criteria for diagnosing and treating patients with TB.6,7 The NTP has a central unit responsible for policy and strategy, while diagnosis, registration and care are decentralised to 57 public or private basic management units (BMUs) in the country.

The present study was conducted in Cotonou and its suburbs, which has a population of about 1 million. There are five BMUs in Cotonou, all of which have a TB register and use TB treatment cards. The GH has a paediatric department and a paediatric surgery department, where children are also diagnosed and treated for TB, but are not notified to the NTP.

Diagnosis and treatment of tuberculosis

Children are suspected of TB if they have chronic symptoms such as cough for >3 weeks, persistent fever, malnutrition, weight loss and/or failure to thrive. The presence of an adult with sputum smear-positive TB living in the same household as the child may be an indication of TB due to contact with the index case. Child TB suspects are investigated using sputum smear microscopy, if they can produce sputum, or, if feasible, gastric lavage, chest radiography (interpreted by radiologists and chest physicians) and tuberculin skin testing. Mycobacterium tuberculosis culture from sputum or other specimens is occasionally performed. Lack of response to non-specific antibiotics may also indicate a diagnosis of TB. If the child’s health status is poor, treatment is started immediately.

At both the NTP facilities and the GH, diagnosed children are classified as pulmonary (smear-positive and smear-negative) and extra-pulmonary TB, and as new and previously treated cases, according to national and international guidelines.6,7 All diagnosed children are supposed to be registered with a BMU close to their homes, and to receive standardised treatment. Children aged <8 years receive rifampicin (RMP), pyrazinamide and isoniazid (INH) for the 2-month initial phase, followed by RMP and INH for the 4-month continuation phase. Treatment for children aged ≥8 years is similar, except that ethambutol is added to the initial phase to make a total of four drugs. At the GH in Cotonou, however, the anti-tuberculosis regimens used do not always follow these recommendations.

For diagnosis, less than US$1 is usually, but not necessarily, required as payment for sputum smear examination at both the GH and the NTP. Treatment is free, and anti-tuberculosis drugs are provided by the NTP (they are not available in private pharmacies). Treatment outcomes are monitored using treatment cards and paper registers at both the NTP and the GH, and NTP outcomes are reported in quarterly reports.

Healthy children aged <5 years and living in the same household as an adult with sputum smear-positive TB are given INH preventive therapy (IPT) for 9 months.

Patients

All children aged 0–14 years who were diagnosed and treated for TB in Cotonou and its suburbs between 1 January 2009 and 31 December 2011 were included in the study. Children who were receiving IPT were excluded.

Data collection

Sources of data were the NTP TB registers and the GH medical files. Diagnosis was made by general practitioners and chest physicians in the NTP and by paediatricians at the GH. Data from each individual patient were collected using a standardised paper-based study questionnaire. To avoid errors, each data variable was collected by two different investigators.

The following data were collected: epidemiological characteristics of the child (sex, age), type and category of TB, HIV status (positive, negative, indeterminate and unknown) and standardised treatment outcomes. For these variables, standardised definitions of the International Union Against Tuberculosis and Lung Disease (The Union) and the World Health Organization (WHO) were used by both the GH and the NTP.8 If the treatment outcome was not known, it was classified as ‘unknown’. Treatment outcomes were ‘successful’ if the children were cured or had completed treatment, and ‘unsuccessful’ if the children died, were lost to follow-up, failed treatment, were transferred out or unknown. A child was classified as ‘still on treatment’ if treatment had not yet been completed.

Statistical analysis

Data from the questionnaire were double-entered into EpiData version 3.1 (EpiData Association, Odense, Denmark). Using frequency analysis, demographic and clinical characteristics and site of diagnosis and care were analysed in relation to treatment outcomes using the χ2 test, relative risks (RRs) and 95% confidence intervals (95%CIs). Comparisons were made using Epi Info, version 6.04dfr (Centers for Disease Control and Prevention, Atlanta, GA, USA). Levels of significance were set at 5%.

Ethics

The study was approved by the Ethics Advisory Group of The Union and the Ethics Committee of the Benin NTP.

RESULTS

Epidemiological characteristics

The number of children treated for TB, all forms, in Cotonou from 2009 to 2011 was 182 (67, 42 and 73 cases respectively in 2009, 2010 and 2011), representing 4.5% of all TB cases notified annually (Table 1). The male:female sex ratio was 0.94; 58 (32%) children were aged <5 years and 124 (68%) were aged between 5 and 14 years. The incidence rate of notified TB cases among children in Cotonou was between 8 and 13/100 000, much lower than that observed among adults (P < 0.01). Reported cases were higher among children aged >5 years (Table 2). One hundred and fifty-three children (84%) were treated at NTP facilities, while 29 children (16%) were treated at the GH but were not notified. Thus, during these 3 years, 16% of all TB cases diagnosed among children were omitted from national figures because they were not notified to the NTP.

TABLE 1.

TB cases, all forms and childhood, in Cotonou, Benin, 2009–2011

Year Notified TB cases n Paediatric TB cases n Proportion of paediatric cases among total cases %
2009 1503 67 4.5
2010 1383 42 3.1
2011 1495 73 4.9

TB = tuberculosis.

TABLE 2.

Estimated population, notified TB cases and incidence of TB in childhood, Cotonou, Benin, 2009–2011

Estimated child population*
Notified cases
Incidence/100 000 children
Incidence/100 000 adults
Year Total <5 years 5–14 years Total <5 years 5–14 years Total <5 years 5–14 years P value ≥15 years P value
2009 506 728 194 709 312 019 67 17 50 13.2 8.7 16.0 <0.01 177.7 <0.01
2010 517 046 199 850 317 196 42 16 26 8.1 8.0 8.2 0.01 160.5 <0.01
2011 527 267 204 404 322 863 73 25 48 13.8 12.2 14.9 <0.01 165.5 <0.01
*

Source: Statistical yearbook of Health Ministry of Benin, 2009, 2010 and 2011.

Comparison between children and adults.

TB = tuberculosis.

Diagnosis of tuberculosis

Table 3 shows TB case notifications by place of treatment (NTP facilities, GH and all sites), stratified by age, sex, type of TB and HIV status. Five times more patients were treated at the NTP facilities than at the GH, and significantly more new sputum smear-positive pulmonary TB (PTB) patients were diagnosed at NTP facilities (P < 0.01), while significantly more extra-pulmonary TB (EPTB) cases were diagnosed at the GH (P < 0.01). HIV status was known for 167 (92%) children, of whom 49 were positive (29%). Significantly more children in the GH did not have their HIV status assessed compared with NTP facilities (P < 0.01).

TABLE 3.

TB cases in children stratified by age, sex, type of TB and HIV status, Cotonou, Benin, 2009–2011

Characteristic NTP facilities n (%) General hospital n (%) All sites n (%) P value*
Total 153 29 182
Age, years
 0–4 45 (29) 13 (45) 58 (32) 0.08
 5–14 108 (71) 16 (55) 124 (68) 0.08
Sex
 Male 73 (48) 15 (52) 88 (48) 0.69
 Female 80 (52) 14 (48) 94 (52) 0.69
Type of TB
 New sputum smear-positive 53 (35) 3 (10) 56 (31) <0.01
 New sputum smear-negative 69 (45) 12 (41) 81 (44) 0.71
 New EPTB 31 (20) 14 (49) 45 (25) <0.01
HIV status
 Positive 43 (28) 6 (21) 49 (27) 0.41
 Negative 106 (69) 12 (41) 118 (65) <0.01
 Unknown 4 (3) 11 (38) 15 (8) <0.01
*

Comparison between NTP and the General Hospital.

Of the total 182 cases, 27% were HIV-positive; of the 167 cases tested, 29% were HIV-positive.

TB = tuberculosis; HIV = human immunodeficiency virus; EPTB = extra-pulmonary TB; NTP = National TB Programme.

Table 4 shows the number of children with different types of EPTB. There were 45 children with EPTB at one site alone, 34 with both PTB and EPTB (registered as PTB cases) and 3 children with EPTB at two sites. The most common sites for EPTB were the lymph nodes, vertebrae and pleura.

TABLE 4.

Number of patients with extra-pulmonary tuberculosis by site of disease, Cotonou, Benin, 2009–2011

Site n (%)
Lymph node 22 (27)
Vertebral 20 (24)
Pleural 17 (21)
Miliary 9 (11)
Peritoneal 4 (5)
Bone (excluding vertebral) 3 (4)
Neuro-meningeal 2 (2)
Pericardial 2 (2)
Cutaneous 2 (2)
Renal 1 (1)
 Total 82 (100)

Treatment outcomes

Of the 182 patients diagnosed, 163 had completed treatment and 19 were still on treatment at the time of data collection. Treatment outcomes, stratified by place, age, sex, type of TB and HIV status, are shown in Table 5. The cure rate was higher among children in the NTP facilities than among those from the GH (P < 0.01), where the rate of unknown outcome was higher. In comparing successful (cure and/or treatment completed) and unsuccessful (death, loss to follow-up and unknown) treatment outcomes between the different groups, successful treatment outcomes were lower in smear-negative than in smear-positive children (RR 0.72, 95%CI 0.58–0.90, P < 0.01), and in HIV-positive compared with HIV-negative children (RR 0.73, 95%CI 0.56–0.96, P < 0.01). All of the HIV-TB co-infected children were on cotrimoxazole preventive therapy. Information about antiretroviral treatment (ART) was not, however, collected during the study. In all other respects, there were no significant differences between the groups.

TABLE 5.

Distribution of treatment outcomes stratified by place of treatment, age, sex, type of TB and HIV status, Cotonou, Benin, 2009–2011

Category Total n Cure and/or treatment completed n (%) Death n (%) LTFU n (%) Outcome unknown n (%)
All cases 163* 118 (72) 14 (9) 12 (7) 19 (12)
Place
 NTP facilities 138 109 (79) 12 (9) 10 (7) 7 (5)
 General Hospital 25 9 (36) 2 (8) 2 (8) 12 (48)
Age, years
 0–4 52 34 (65) 6 (12) 5 (10) 7 (14)
 5–14 111 84 (76) 8 (7) 7 (6) 12 (11)
Sex
 Male 79 60 (76) 5 (6) 4 (5) 10 (13)
 Female 84 58 (69) 9 (11) 8 (10) 9 (11)
Type of TB
 New smear-positive TB 49 42 (86) 3 (6) 0 4 (16)
 New smear-negative TB 71 44 (62) 9 (13) 9 (13) 9 (13)
 New EPTB 43 32 (74) 2 (5) 3 (7) 6 (14)
HIV status
 Positive 45 26 (58) 6 (13) 5 (11) 8 (18)
 Negative 104 82 (79) 8 (8) 5 (5) 9 (9)
 Unknown 14 0 10 (71) 2 (14) 2 (14)
*

Number of children who completed follow-up for treatment.

TB = tuberculosis; HIV = human immunodeficiency virus; LTFU = loss to follow-up; NTP = National TB Control Programme; EPTB = extra-pulmonary TB.

DISCUSSION

The study is the first in Benin to describe the burden of TB and treatment outcomes among children in Cotonou, and this in turn has a direct influence on results at a national level. Our main findings were a treatment rate among children that was lower than WHO global estimates (4.5% vs. 11% of total cases) and a higher proportion of children treated in the age group 5–14 years than among younger children (68% vs. 32%). Approximately 16% of the children were diagnosed and treated at the GH and were not notified, contributing to an underreporting of the true burden of childhood TB in Cotonou and Benin. As a greater proportion of children at the GH were diagnosed with EPTB, this type of TB is particularly underreported. This may also be due to misdiagnosis due to lack of training in childhood TB among health care workers, as training in TB generally focuses on the detection of smear-positive TB in adults.

Reports about TB prevalence being higher in younger children are conflicting.914 Although younger children are at greater risk of progressing to active TB once infected with M. tuberculosis, they were underrepresented in our study, possibly due to misdiagnosis.1518 For example, TB in younger children presenting with acute pneumonia or malnutrition may be missed due to clinical overlap with other common child illnesses, and die due to TB. In addition, collecting adequate sputum specimens in this young age group is very difficult. Studies increasingly advocate the implementation of other sampling methods, such as induced sputum, in primary health care settings.19,20

This study was conducted in an urban setting, with a low rate of children being diagnosed and treated for TB. We assume that this rate is even lower in rural settings due to the shortage of specialists and difficulty in accessing health care services.

The predominance of lymph node, pleural and spinal TB among EPTB patients (72%) is similar to that reported in Malawi (62%).21 We found TB meningitis to be rare, however, in contrast to the higher rates reported elsewhere.22 Reasons for this may include difficulty in confirming the diagnosis, and bacille Calmette-Guérin vaccination coverage of almost 100% in Benin, which protects children against severe forms of TB such as TB meningitis and miliary disease.23,24

It should be noted that although Benin is not a high-burden country for HIV (1.7%), HIV prevalence among children with TB was high (29%), and much higher than in adults (15%). A limitation of our study is that data on ART were not recorded. However, WHO recommendations for ART were applied on the whole.25 The number of maternity wards involved in preventive mother-to-children treatment is increasing (61% in 2012), and there is a transition to three-drug prophylaxis. However, full coverage of pregnant women has not yet been achieved (51% in 2010).

Treatment outcomes among the children were reasonable. The overall treatment success rate, at 72%, was higher than that reported in Malawi (45%),21 but lower than in Djibouti in 2010 (84%).26 A higher treatment success rate of 86% in smear-positive cases was close to that reported for adults (90%);2 overall better treatment outcomes could be obtained through better monitoring systems to reduce loss to follow-up and unknown outcomes, and possibly by more accurate diagnosis. For example, unknown outcomes were particularly common in children registered and treated at the GH. This may be related to misdiagnosis (with consequent discontinuation) or lack of information on treatment duration. Referring children to BMUs (where health care workers trace all patients lost to follow-up) for their treatment monitoring may be one solution. Appointments would also be set with the GH practitioner. Unsurprisingly, worse outcomes were observed in smear-negative and HIV-infected children, as the TB diagnosis in both cases was doubtful.

In conclusion, childhood TB makes up a small proportion of all reported TB cases in Cotonou, Benin. While treatment outcomes are reasonable, particularly for smear-positive cases, better follow-up and monitoring is needed during treatment to reduce the high burden of loss to follow-up and unknown outcomes. Greater collaboration between the NTP and the General Hospital is required to improve case notification and treatment outcomes, and we have been working to address these issues since the completion of the study.

Acknowledgments

The authors thank G Hounnou and collaborators in the paediatric departments of the General Hospital for their contribution in accessing medical files. They also thank the National Tuberculosis Programme staff and the University of Bergen, Bergen, Norway, for their technical and financial support.

The publication of this research was supported through an operational research course that was jointly developed and run by the Centre for Operational Research, International Union Against Tuberculosis and Lung Disease (The Union); The Union South-East Asia Office, New Delhi, India; and the Operational Research Unit, Médecins Sans Frontières, Brussels Operational Centre, Luxembourg.

Funding for this course came from an anonymous donor and the Department for International Development, UK.

Conflict of interest: none declared.

References

  • 1.Swaminathan S, Rekha B. Pediatric tuberculosis: global overview and challenges. Clin Infect Dis. 2010;50(Suppl 3):S184–S194. doi: 10.1086/651490. [DOI] [PubMed] [Google Scholar]
  • 2.World Health Organization. Global tuberculosis report 2011. WHO/HTM/TB/2011.16. Geneva, Switzerland: WHO; 2011. [Google Scholar]
  • 3.Nelson L J, Wells C D. Global epidemiology of childhood tuberculosis. Int J Tuberc Lung Dis. 2004;8:636–647. [PubMed] [Google Scholar]
  • 4.World Health Organization. Guidance for national tuberculosis programmes on the management of tuberculosis in children. WHO/HTM/TB/2006.371. WHO/FCH/CAH/2006.7. Geneva, Switzerland: WHO; 2006. [PubMed] [Google Scholar]
  • 5.Delacourt C. Specific features of tuberculosis in childhood. Rev Mal Respir. 2011;28:529–541. doi: 10.1016/j.rmr.2010.10.038. [DOI] [PubMed] [Google Scholar]
  • 6.National Tuberculosis Control Programme. National tuberculosis guide. Cotonou, Benin: NTP. 2009 http://www.pnt-benin.bj/spip.php?article48 Accessed December 2012. [Google Scholar]
  • 7.National Tuberculosis Control Programme. Extra-pulmonary and smear-negative pulmonary tuberculosis guide. Cotonou, Benin: NTP; 2008. http://www.pnt-benin.bj/spip.php?article48 Accessed December 2012. [Google Scholar]
  • 8.World Health Organization/International Union Against Tuberculosis and Lung Disease/KNCV. Revised international definitions in tuberculosis control. Int J Tuberc Lung Dis. 2001;5:213–215. [PubMed] [Google Scholar]
  • 9.Van Rie A, Beyers N, Gie R P, Kunneke M, Zietsman L, Donald P R. Childhood tuberculosis in an urban population in South Africa: burden and risk factor. Arch Dis Child. 1999;80:433–437. doi: 10.1136/adc.80.5.433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Marais B J, Gie R P, Schaaf H S, Hesseling A C, Enarson D A, Beyers N. The spectrum of disease in children treated for tuberculosis in a highly endemic area. Int J Tuberc Lung Dis. 2006;10:732–738. [PubMed] [Google Scholar]
  • 11.Lobato M N, Cummings K, Will D, Royce S. Tuberculosis in children and adolescents: California, 1985 to 1995. Pediatr Infect Dis J. 1998;17:407–411. doi: 10.1097/00006454-199805000-00012. [DOI] [PubMed] [Google Scholar]
  • 12.Nelson L J, Schneider E, Wells C D, Moore M. Epidemiology of childhood tuberculosis in the United States, 1993–2001: the need for continued vigilance. Pediatrics. 2004;114:333–341. doi: 10.1542/peds.114.2.333. [DOI] [PubMed] [Google Scholar]
  • 13.Ouattara K, Soumare D N, Morba A, et al. Profil de la tuberculose chez l’enfant en milieu hospitalier [Affiche scientifique] Rev Mal Respir. 2012;29(Suppl 1):A1–A229. [French] [Google Scholar]
  • 14.Zemour L, Belghitri A, Chougrani S, Sari N. Profil épidémiologique de la tuberculose chez l’enfant à Remchi (2000–2011) [Affiche scientifique] Rev Mal Respir. 2012;29(Suppl 1):A1–A229. [French] [Google Scholar]
  • 15.Particularités de la tuberculose pédiatrique. Rev Mal Respir. 2003;20:7S52–7S55. [French] [PubMed] [Google Scholar]
  • 16.Rieder H L. Epidemiology of tuberculosis in children. Annales Nestlé. 1997;55:1–9. [Google Scholar]
  • 17.Dufour V. Tuberculose et collectivités d’enfants. Rev Mal Respir. 2008;25:117–119. [French] [Google Scholar]
  • 18.International Union Against Tuberculosis and Lung Disease. Desk-guide for diagnosis and management of TB in children. Paris, France: The Union; 2010. [Google Scholar]
  • 19.Hatherill M, Hawkridge T, Zar H, et al. Induced sputum or gastric lavage for community-based diagnosis of childhood pulmonary tuberculosis? Arch Dis Child. 2009;94:195–201. doi: 10.1136/adc.2007.136929. [DOI] [PubMed] [Google Scholar]
  • 20.Zar H J, Hanslo D, Apolles P, et al. Induced sputum versus gastric lavage for microbiological confirmation of pulmonary tuberculosis in infants and young children: a prospective study. Lancet. 2005;365:130–134. doi: 10.1016/S0140-6736(05)17702-2. [DOI] [PubMed] [Google Scholar]
  • 21.Harries A D, Hargreaves N J, Graham S M, et al. Childhood tuberculosis in Malawi: nationwide case-finding and treatment outcomes. Int J Tuberc Lung Dis. 2002;6:424–431. [PubMed] [Google Scholar]
  • 22.Lestari T, Probandari A, Hurtig A-K, Utarini A. High caseload of childhood tuberculosis in hospitals on Java Island, Indonesia: a cross sectional study. BMC Public Health. 2011;11:784. doi: 10.1186/1471-2458-11-784. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Ministère de la Santé. Annuaire des statistiques sanitaires de l’année 2009. Cotonou, Bénin: Ministère de la Santé. 2009 [French] [Google Scholar]
  • 24.Trunz B, Fine P, Dye C. Effect of BCG vaccination on childhood tuberculous meningitis and miliary tuberculosis worldwide: a meta-analysis and assessment of cost-effectiveness. Lancet. 2006;367:1173–1180. doi: 10.1016/S0140-6736(06)68507-3. [DOI] [PubMed] [Google Scholar]
  • 25.World Health Organization. HIV/AIDS Programme. Antiretroviral therapy of HIV infection in infants and children: towards universal access. Recommendations for a public health approach. 2010 revision. Geneva, Switzerland: WHO; 2010. [PubMed] [Google Scholar]
  • 26.Kamaté M, Osman M, Mohamed Y, Hoche S. Prise en charge de la tuberculose chez l’enfant en 2010 au Centre Paul-Faure de Djibouti [Affiche scientifique] Rev Mal Respir. 2012;29(Suppl 1):A1–A229. [French] [Google Scholar]

Articles from Public Health Action are provided here courtesy of The International Union Against Tuberculosis and Lung Disease

RESOURCES