This article has Open Peer Review reports available.
The effect of HIV and antiretroviral therapy on characteristics of pulmonary tuberculosis in northern Malawi: a cross-sectional study
© Munthali et al.; licensee BioMed Central Ltd. 2014
Received: 22 July 2013
Accepted: 19 February 2014
Published: 25 February 2014
HIV infection reduces the likelihood that individuals with pulmonary tuberculosis are smear positive and that they have cavitatory disease. Antiretroviral therapy (ART) may shift the pattern of disease to be more similar to that of HIV negative patients. This would aid diagnosis- which often depends on sputum smears – but would also increase infectiousness. We assessed the effect of HIV and ART on smear positivity and cavitatory disease in laboratory-confirmed pulmonary TB patients.
Three sputum samples were collected per pulmonary TB suspect and were examined using microscopy and culture. Chest radiographs were available for a subset of patients as part of another study. The effect of HIV and ART status on sputum smear positivity and lung cavitation were evaluated using multivariable logistic regression.
Of 1024 laboratory-confirmed pulmonary TB patients who were identified between January 2005 and December 2011, 766 had HIV and ART status available. Positive sputum smears were significantly more common among HIV negative individuals than HIV positive individuals (adjusted OR = 2.91, 95% CI 1.53 – 5.55). Compared to those HIV positive but not on ART, patients on ART were more likely to be smear positive (adjusted OR = 2.33, 95% CI 1.01 – 5.39) if they had been on ART ≤ 6 months, but only slightly more likely to be smear positive (adjusted OR = 1.43, 95% CI 0.68 – 2.99) if they were on ART > 6 months. HIV negative patients were more likely than HIV positive patients to have cavitatory disease (adjusted OR = 1.97, 95% CI 1.20 – 3.23). Patients on ART > 6 months had a slight increase in cavitatory disease compared to HIV positive patients not on ART (adjusted OR = 1.68, CI 0.78 – 3.63).
HIV infection is associated with less smear positivity and cavitation in pulmonary TB patients. Among HIV positive patients, the use of ART shifts the presentation of disease towards that seen in HIV-negative individuals, which facilitates diagnosis but which also could increase infectiousness.
KeywordsSmear positivity Cavitation HIV ART Infectiousness Culture Malawi
Tuberculosis (TB) is a major public health challenge. Globally there were an estimated 8.7 million incident cases of TB in 2011, 26% of which occurred in Africa, and 1.4 million TB deaths . 13% (1.1 million) of the incident cases were HIV positive. In Malawi the number of TB cases notified to the National TB Control Programme rose sharply from 12,395 (132 per 100,000 population) in 1990 to 25,491 (199 per 100,000 population) in 2005 . The upsurge in TB was largely due to HIV infection. HIV increases the risk of rapid TB progression after primary infection or re-infection with Mycobacterium tuberculosis (Mtb) and increases the risk of reactivating latent TB infection [3, 4]. In HIV negative individuals infected with Mtb, the lifetime risk of developing TB disease is between 10% and 20% while in those co-infected with HIV the annual risk is 10% or more [5, 6].
The Malawi government, with assistance from the Global Fund on Tuberculosis, Malaria and HIV/AIDS, started provision of antiretroviral therapy (ART) to HIV-infected eligible individuals in 2004. By mid-2006 there were 94 facilities providing ART and the total number of patients alive and on ART was 41,549 . The provision of ART has been widely scaled up including the introduction of “Option B+” in Malawi in July 2011 with which all HIV-infected pregnant and breastfeeding women are started on lifelong ART regardless of clinical or immunological stage. By the end of 2012 there were 651 static ART sites and 585 sites providing Option B+ and a total of 404,905 HIV-infected individuals on ART . Since the introduction and rolling out of ART in Malawi TB notification rates have started to decline, with 25,491 (199 per 100,000 population) in 2005, 23,929 (171 per 100,000 population) in 2008, 22, 674 (157 per 100,000 population) in 2009 and 21,092 (142 per 100,000 population) in 2010 . In HIV-infected individuals, ART reduces the incidence of TB, although rates remain higher than in HIV negative patients [9–11].
Sputum smear microscopy has been the backbone for the diagnosis of pulmonary TB in most low-income countries because of its low cost, and is directly related to infectiousness [12–14]. Due to paucibacillary pulmonary disease in patients infected with HIV, the use of smear microscopy in the diagnosis of pulmonary TB is not ideal, although widely used . In HIV-infected, immunocompromised individuals, lung cavitation is less frequent because the defective specific cell-mediated immune response reduces the ability to mount a granulomatous response to Mtb[15, 16].
ART is widely used and has significantly improved the prognosis of HIV-infected patients. The objective of this study is to assess the effect of HIV and ART on the presence of smear positivity and cavitation at diagnosis of laboratory-confirmed pulmonary TB, and to understand if ART may affect infectiousness of HIV positive TB patients.
Karonga district is situated in northern Malawi and has a population of approximately 300,000 . The district has a district hospital and several health centres. The Karonga Prevention Study has been conducting research on tuberculosis in the district since 1988. Pulmonary TB cases were identified through enhanced passive surveillance: individuals with a cough of at least two weeks visiting health facilities within the district were investigated for pulmonary TB. Individuals were also identified by community screening in the context of other related research studies, but this practice yielded few cases. Individuals suspected of having pulmonary TB were asked to submit three sputum specimens, one collected on-the- spot, a second early morning specimen and a third specimen collected on-the-spot at the time of delivery of the second specimen, as per Malawi National TB Programme guidelines [18, 19].
Sputum smear examination was performed at the research project laboratory using fluorescence microscopy with auramine staining, with confirmation of positive smears by light microscopy using Ziehl-Neelsen (ZN) stain. All sputum specimens were then cultured using Lowenstein- Jensen solid media . Cultures suggestive of TB were sent to the National Mycobacterium Reference Laboratory (Health Protection Agency) in the UK for species confirmation and drug sensitivity testing.
A pulmonary TB case was defined as being laboratory confirmed if at least one sputum smear or culture was positive. Those with no positive culture and only a single scanty smear (<10 acid-fast bacilli per 100 High Powered Fields) were excluded.
Study population, data collection and statistical methods
All confirmed pulmonary TB cases in Karonga District aged ≥15 years and diagnosed between January 2005 and December 2011 were included in the study. After written informed consent, study participants were interviewed using a standard structured questionnaire. In individuals aged <18 years a written informed consent was obtained from their parents or guardians at the time of the interview. Patients were asked about sociodemographic characteristics and history of previous TB.
Chest radiographs were available for a group of patients, most of whom were enrolled in immunological studies. The objective of these studies was to develop a rapid, sensitive, and affordable biological marker (genomic or proteomic) for diagnosis of TB. Inclusion criteria for immunological studies included: willingness to undergo an HIV test and give a venous blood sample, and aged 18 years or over. Exclusion criteria were a past history of cancer, taking steroids in the past 6 months, pregnancy and diabetes: few individuals were excluded for these reasons. Radiographs were independently reviewed by a chest physician or a radiologist following a standardised format that assessed the presence of cavitation, parenchymal consolidation, pleural effusion, miliary pattern infiltrates and other radiological abnormalities. These readers were blinded to the HIV and ART status of the patients. They were also blinded to the diagnosis of the patient, which was possible because they were also reviewing chest radiographs for individuals with illnesses other than TB.
Pulmonary TB patients were pre and post-test counselled for HIV by trained counsellors. After interview and if written consent was given blood was taken. In 2005 – 2007, HIV testing was done using ELISA (Vironostika; Organon Teknika, Cambridge, UK) and particle agglutination test (Edgeware modification of the Serodia). Positives were confirmed using a further ELISA (Wellcozyme Wellcome Diagnostics, Dartford, UK or Enzygnost, Behring, Marburg, Germany) and particle agglutination test assay (Serodia, Fujirebio Inc, Tokyo, Japan). Samples giving discrepant results were repeated in duplicates using the same two tests. From 2007, HIV testing was done using Determine (Abbot Japan Co, Tokyo, Japan). Positives were confirmed using Uni-Gold (Trinity Biotech plc, Bray, Ireland). For any discrepant results Bioline (Standard Diagnostics, Giheung-gu, Korea) was used. Patients who were known to be HIV positive at the time of TB diagnosis were asked about ART use. Free ART was available in the District from 2005. As well as patients’ self-reports, information on ART use was collected from patient-held “health passports” which record details of treatments. Further data on ART usage was also available from linked studies in local ART clinics, which involve identifying patients on ART, if they give consent.
Statistical analysis was performed using STATA 11© software (StataCorp, TX, USA). Patients were grouped as ‘not on ART’, ‘on ART ≤6 months’, ‘on ART >6 months’ or ‘HIV negative’. Duration on ART was included to differentiate the effect of prolonged improved immune function from the early period in which TB could result from unmasking or continued poor immunity . The main analysis was restricted to pulmonary TB cases with known HIV status. The effects of HIV and ART status were evaluated using multivariable logistic regression with sputum smear positivity (among 766 study participants) and cavitation (among a subset of 310 study participants) as the outcome variables.
The data were derived from studies approved by the Malawi National Health Sciences Research Committee which is the local ethics committee and the Ethics Committee of the London School of Hygiene & Tropical Medicine.
Characteristics of the study population
Those with unknown HIV status were older than patients with known HIV status but there was no evidence for other differences in terms of gender or socio-economic status. There were differences in age, sex and socio-economic characteristics between HIV negative and HIV positive patients. HIV negative patients were older, more commonly male, more likely to be farmers and to have received less education. Previous TB was more common in HIV positive patients, particularly those who had been on ART for more than 6 months.
Prevalence of sputum smear positivity and cavitation by patient characteristics among pulmonary TB patients
HIV positive not on ART
HIV positive on ART 0 – 6 months
HIV positive on ART >6 months
History of previous TB
15 – 29
30 – 44
45 – 59
Never or lower primary
Chest radiographs were available for 310 (40%) of the 766 patients. A higher proportion of HIV negative patients had chest radiographs, and these were slightly more common in men, but there was no evidence that having a chest radiograph was associated with age, or socio-economic status of the study participant.
Smear positivity and cavitation
Overall, 691 (90%) of the 766 patients had at least one sputum smear positive for acid-fast bacilli, and 158 (51%) of the 310 patients with X-rays had evidence of cavitation (Table 1). The proportion smear positive was higher in HIV negative patients (95%) than in HIV positive patients (88%). Among those who were HIV positive, the proportion smear positive was highest for those on ART for less than 6 months (93%) and lowest in those not on ART (85%). Cavitation was more common in the HIV negative (59%) than in those who were HIV positive (44%). It was present in 54% of those on ART for >6 months and 40% of those not on ART.
Association of HIV and ART status with sputum smear positivity (amongst 766 participants) and cavitation (amongst 310 participants)
Smear positivity (n = 766)
Cavitation (n = 310)
Adjusted for age and sex
Adjusted for age and sex
Crude OR (95% CI)
Adj OR (95% CI)
Crude OR (95% CI)
Adj OR (95% CI)
2.44 (1.37 – 4.32)
2.91 (1.53 – 5.55)
1.83 (1.17 – 2.88)
1.97 (1.20 – 3.23)
HIV positive not on ART
HIV positive on ART 0 – 6 months
2.31 (1.00 – 5.31)
2.33 (1.01 – 5.39)
1.02 (0.47 – 2.22)
0.92 (0.41 – 2.03)
HIV positive on ART >6 months
1.41 (0.67 – 2.93)
1.43 (0.68 – 2.99)
1.70 (0.80 – 3.61)
1.68 (0.78 – 3.63)
After adjusting for age and sex, HIV negativity was associated with nearly twice the odds of cavitation of those who were HIV positive (adjusted OR = 1.97, 95% CI 1.20 – 3.23). HIV positive individuals who were on ART > 6 months had more than one and half times increase in the odds of cavitation as compared to HIV positive patients not on ART (adjusted OR = 1.68, CI 0.78 – 3.63). Adjustment for other possible confounders (history of TB, level of education and occupation) made little difference to the results for smear positivity or cavitation.
This study shows that smear positivity and radiological changes in laboratory confirmed TB patients diagnosed in a rural northern Malawian population were affected by the individual’s HIV and ART status. HIV-infected individuals were significantly less likely to have positive sputum smears and lung cavitation than those who were HIV negative, as found elsewhere [6, 22]. ART appears to increase smear positivity and cavitation in HIV positive individuals although the proportions remained lower than in HIV negative individuals.
Many studies have looked at ART and its effect on survival in HIV-infected individuals [23, 24]. Fewer studies have described the role of ART in the evaluation of people suspected of having TB . Tiffany et al. found that among HIV positive TB patients in the US those who were diagnosed in the late ART era were more likely to have a positive smear compared to those diagnosed in the early ART era . A study in Italy found that cavitation was more common in HIV infected TB patients who were on ART compared to those not on ART . Sharma et al. in India showed that HIV positive individuals with a moderate functional immune system diagnosed with pulmonary TB had sputum smears that were more likely to be positive for acid fast bacilli than those with higher levels of immunosuppression .
The positive association between ART and smear positivity and cavitation suggests that ART may play a role in shifting the disease pattern towards a more typical appearance, similar to that found in HIV negative individuals due to restoration of immune function. An increasing proportion of HIV–infected TB patients are likely to present with a laboratory confirmed TB diagnosis or a typical radiographic appearance on a chest radiograph. The introduction of ART among HIV–infected individuals co-infected with TB could be one of the most important factors in modifying the clinical presentation of TB disease in HIV infected individuals. Advanced HIV disease is known to be associated with lower rates of sputum smear positivity and therefore less infectivity . In this new era in which many countries have scaled up ART delivery, ART could result in increased infectiousness of an individual as improved immune status shifts towards sputum smear positivity. With the move towards integrated HIV/TB care, the potential for transmission of M. tuberculosis in clinic settings is increased. WHO has recommended implementation of TB infection control measures, especially in healthcare facilities providing HIV care. These measures include a TB infection control plan comprised of managerial (e.g. use of building space, on-going TB surveillance of healthcare workers); administrative (e.g. triage to identify people with TB symptoms, separation of infectious cases, reduction of waiting times); environmental (e.g. maximising ventilation systems) and personal protection measures (e.g. use of N95 particulate respirators by healthcare workers) to reduce nosocomial TB transmission. Individuals living with HIV should be provided with ART and isoniazid preventive therapy if eligible .
In the study 25% of eligible study participants had unknown HIV status. This should not affect the comparisons of HIV positive and negative individuals, and since those with unknown status had similar socio-demographic characteristics as those with known status it should not affect generalisability of the results. The high proportion smear positive in this study may be partly attributed to restriction of the study to those who were smear or culture positive, and to examining smears in a research environment using fluorescence microscopy, which may not be readily available under routine health services and which has been shown to be more sensitive than ZN microscopy . CD4 cell counts were not routinely available so we were unable to explore how the immune status affected the smear status. Although some patients self-reported their ART status, the availability of data from health passports and ART registered patients in the district is likely to have minimised misclassification.
Only 310/766 (40%) of the pulmonary TB cases had chest radiographs. Some of the patients probably had missing radiographs because they had died before a radiograph could be taken. Since chest radiographs were mainly done in individuals eligible for immunological studies, which excluded pregnant women and individuals taking steroids or suffering from diabetes or cancer, this could have affected generalisability of the results, but only 14 (1.8%) of the laboratory-confirmed pulmonary TB patients with known HIV status were excluded from immunological studies based on these criteria. Although there were some differences in gender and HIV prevalence between those who had a radiograph and those who did not, there was little difference by age, socio-economic status or clinical presentation.
The sample size for this analysis was small so there was limited power to investigate effects by duration of ART. Some patients might have had active subclinical disease at the time of ART initiation and presentation of symptomatic disease might have arisen from ART-induced restoration of an immune reaction against M. tuberculosis (unmasking) . There is a suggestion that cavitation was more common later, which would be expected with further improvement in immune function .
Wide scaling up of ART in developing countries and early initiation of treatment is likely to change the clinical presentation among TB patients with HIV co-infection to a pattern more similar to that in HIV negative TB patients. While this is more easily diagnosed, especially in settings relying on sputum microscopy, it is also more infectious than the disease in HIV co-infected TB patients who are ART-naive. Infection control measures in ART clinics are important to limit the spread of TB.
We thank the TB patients of Karonga District for their willing participation. We are grateful to our field staff particularly L Sichali, L Mwaungulu and V Mwinuka. We are also thankful to B Mhango from the Malawi National TB Programme for collaboration. We are also indebted to our funders.
This work was funded by the Wellcome Trust, the European Union and Bill and Melinda Gates foundation.
- World Health Organization: Global Tuberculosis Report 2012. 2012, Geneva, Switzerland: WHO, http://www.who.int/tb/publications/global_report/gtbr12_main.pdf,Google Scholar
- World Health Organization: Global Tuberculosis Control 2011. 2011, Geneva, Switzerland: WHO, http://www.who.int/tb/publications/global_report/2011/en/,Google Scholar
- De Cock KM, Chaisson RE: Will DOTS do it? A reappraisal of tuberculosis control in countries with high rates of HIV infection. Int Tuberc Lung Dis. 1999, 3 (4): 457-465.Google Scholar
- Crampin AC, Glynn JR, Fine PE: What has Karonga taught us? Tuberculosis studied over three decades. Int J Tuberc Lung Dis. 2009, 13 (2): 153-164.PubMedPubMed CentralGoogle Scholar
- Habib AG: A clinical and epidemiologic update on the interaction between tuberculosis and human immunodeficiency virus infection in adults. Ann Afr Med. 2009, 8 (3): 147-155.PubMedGoogle Scholar
- Oni T, Patel J, Gideon HP, Seldon R, Wood K, Hlombe Y, Wilkinson KA, Rangaka MX, Mendelson M, Wilkinson RJ: Enhanced diagnosis of HIV-1-associated tuberculosis by relating T-SPOT.TB and CD4 counts. Eur Respir J. 2010, 36 (3): 594-600. 10.1183/09031936.00171509.View ArticlePubMedPubMed CentralGoogle Scholar
- Ntata PRT: Equity in access to ARV drugs in Malawi. J Soc Aspects HIV/AIDS. 2007, 4 (1): 564-574. 10.1080/17290376.2007.9724818.View ArticleGoogle Scholar
- HIV Unit: Malawi Ministry of Health: Integrated HIV Program Report October - December 2012. 2013, Lilongwe, M alawi, http://www.hivunitmohmw.org/uploads/Main/Quarterly_HIV_Programme_Report_2012_Q4.pdf,Google Scholar
- Girardi E, Palmieri F, Angeletti C, Vanacore P, Matteelli A, Ippolito G: Impact of previous ART and of ART initiation on outcome of HIV-associated tuberculosis. Clin Dev Immunol. 2012, 14 (Suppl 3): S47-S56.Google Scholar
- Lawn SD, Badri M, Wood R: Tuberculosis among HIV-infected patients receiving HAART: long term incidence and risk factors in a South African cohort. AIDS. 2005, 19 (18): 2109-2116. 10.1097/01.aids.0000194808.20035.c1.View ArticlePubMedGoogle Scholar
- Girardi E, Sabin CA, d’Arminio Monforte A, Hogg B, Phillips AN, Gill MJ, Dabis F, Reiss P, Kirk O, Bernasconi E, Grabar S, Justice A, Staszewski S, Fatkenheuer G, Sterne GA: Incidence of tuberculosis among HIV-infected patients receiving highly active antiretroviral therapy in Europe and North America. Clin Infect Dis. 2005, 41 (12): 1772-1782.View ArticlePubMedGoogle Scholar
- Ramsay A, Cuevas LE, Mundy CJ, Nathanson CM, Chirambo P, Dacombe R, Squire SB, Salaniponi FM, Munthali S: New policies, new technologies: modelling the potential for improved smear microscopy services in Malawi. PLoS One. 2009, 4 (11): e7760-10.1371/journal.pone.0007760.View ArticlePubMedPubMed CentralGoogle Scholar
- Ramsay A, Bonnet M, Gagnidze L, Githui W, Varaine F, Guerin PJ: Sputum, sex and scanty smears: new case definition may reduce sex disparities in smear-positive tuberculosis. Int J Tuberc Lung Dis. 2009, 13 (5): 613-619.PubMedGoogle Scholar
- Siddiqi K, Walley J, Khan MA, Shah K, Safdar N: Clinical guidelines to diagnose smear-negative pulmonary tuberculosis in Pakistan, a country with low-HIV prevalence. Trop Med Int Health. 2006, 11 (3): 323-331. 10.1111/j.1365-3156.2006.01559.x.View ArticlePubMedGoogle Scholar
- Doenhoff MJ: Granulomatous inflammation and the transmission of infection: schistosomiasis–and TB too?. Immunol Today. 1998, 19 (10): 462-467.View ArticlePubMedGoogle Scholar
- Garcia GF, Moura AS, Ferreira CS, Rocha MO: Clinical and radiographic features of HIV-related pulmonary tuberculosis according to the level of immunosuppression. Rev Soc Bras Med Trop. 2007, 40 (6): 622-626.View ArticlePubMedGoogle Scholar
- National Statistical Office: 2008 Malawi Population and Housing Census. 2009, Zomba, Malawi, http://www.nsomalawi.mw/index.php/2008-population-and-housing-census.html,Google Scholar
- Crampin AC, Glynn JR, Floyd S, Malema SS, Mwinuka VK, Ngwira BM, Mwaungulu FD, Warndoff DK, Fine PE: Tuberculosis and gender: exploring the patterns in a case control study in Malawi. Int J Tuberc Lung Dis. 2004, 8 (2): 194-203.PubMedGoogle Scholar
- Crampin AC, Floyd S, Mwaungulu F, Black G, Ndhlovu R, Mwaiyeghele E, Glynn JR, Warndoff DK, Fine PE: Comparison of two versus three smears in identifying culture-positive tuberculosis patients in a rural African setting with high HIV prevalence. Int J Tuberc Lung Dis. 2001, 5 (11): 994-999.PubMedGoogle Scholar
- Crampin AC, Mwaungulu JN, Mwaungulu FD, Mwafulirwa DT, Munthali K, Floyd S, Fine PE, Glynn JR: Recurrent TB: relapse or reinfection? The effect of HIV in a general population cohort in Malawi. AIDS. 2010, 24 (3): 417-426. 10.1097/QAD.0b013e32832f51cf.View ArticlePubMedPubMed CentralGoogle Scholar
- Lawn SD, Wilkinson RJ, Lipman MCI, Wood R: Immune reconstitution and “unmasking” of tuberculosis during antiretroviral therapy. Am J Respir Crit Care Med. 2008, 177: 680-685. 10.1164/rccm.200709-1311PP.View ArticlePubMedPubMed CentralGoogle Scholar
- Chamie G, Luetkemeyer A, Walusimbi-Nanteza M, Okwera A, Whalen CC, Mugerwa RD, Havlir DV, Charlebois ED: Significant variation in presentation of pulmonary tuberculosis across a high resolution of CD4 strata. Int J Tuberc Lung Dis. 2010, 14 (10): 1295-1302.PubMedPubMed CentralGoogle Scholar
- Akksilp S, Karnkawinpong O, 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): 1001-1007. 10.3201/eid1307.061506.View ArticlePubMedPubMed CentralGoogle Scholar
- Franke MF, Robins JM, Mugabo J, Kaigamba F, Cain LE, Fleming JG, Murray MB: Effectiveness of early antiretroviral therapy initiation to improve survival among HIV-infected adults with tuberculosis: a retrospective cohort study. PLoS Med. 2011, 8 (5): e1001029-10.1371/journal.pmed.1001029.View ArticlePubMedPubMed CentralGoogle Scholar
- Dembele M, Saleri N, Migliori GB, Ouedraogo H, Carvalho AC, Ouedraogo M, Badoum G, Matteelli A: High incidence of sputum smear negative tuberculosis during HAART in Burkina Faso. Eur Respir J. 2008, 32 (6): 1668-1669. 10.1183/09031936.00106308.View ArticlePubMedGoogle Scholar
- Harris TG, Li J, Hanna DB, Munsiff SS: Changing sociodemographic and clinical characteristics of tuberculosis among HIV-infected patients, New York City, 1992–2005. Clin Infect Dis. 2010, 50 (11): 1524-1531. 10.1086/652654.View ArticlePubMedGoogle Scholar
- Rizzi EB, Schinina V, Palmieri F, Girardi E, Bibbolino C: Radiological patterns in HIV-associated pulmonary tuberculosis: comparison between HAART-treated and Non-HAART-treated patients. Clin Radiol. 2003, 58: 469-473. 10.1016/S0009-9260(03)00056-4.View ArticleGoogle Scholar
- Sharma SK, Mohan A, Kadhiravan T: HIV-TB co-infection: epidemiology, diagnosis & management. Indian J Med Res. 2005, 121 (4): 550-567.PubMedGoogle Scholar
- Mugusi F, Villamor E, Urassa W, Saathoff E, Bosch RJ, Fawzi WW: HIV co-infection, CD4 cell counts and clinical correlates of bacillary density in pulmonary tuberculosis. Int J Tuberc Lung Dis. 2006, 10 (6): 663-669.PubMedGoogle Scholar
- WHO policy on collaborative TB/HIV activities: Guidelines for National Programmes and other Stakeholders. 2012, Geneva: World Health OrganizationGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/14/107/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.