Effectiveness of isoniazid preventative therapy in reducing incidence of active tuberculosis among people living with HIV/AIDS in public health facilities of Addis Ababa, Ethiopia: a historical cohort study
Identifieur interne : 000622 ( Pmc/Corpus ); précédent : 000621; suivant : 000623Effectiveness of isoniazid preventative therapy in reducing incidence of active tuberculosis among people living with HIV/AIDS in public health facilities of Addis Ababa, Ethiopia: a historical cohort study
Auteurs : Mahlet Semu ; Teferi Gedif Fenta ; Girmay Medhin ; Dawit AssefaSource :
- BMC Infectious Diseases [ 1471-2334 ] ; 2017.
Abstract
Human Immunodeficiency Virus (HIV) pandemic has exacerbated tuberculosis disease especially in Sub-Saharan African countries. The World Health Organization (WHO) and Joint United Nations Program on HIV/AIDS (UNAIDS) have recommended Isoniazid Preventive Therapy (IPT) for HIV infected patients to reduce the burden of tuberculosis (TB). Ethiopia has been implementing IPT since 2007. However, effectiveness of IPT in averting occurrence of active tuberculosis among HIV infected patients has not been assessed.
Retrospective cohort study was employed using secondary data from public health institutions of Addis Ababa. Descriptive statistics and Generalized Linear Model based on Poisson regression was used for data analysis.
From 2524 HIV infected patients who were followed for 4106 Person-Years, a total of 277 incident Tuberculosis (TB) cases occurred. TB Incidence Rate was 0.21/100 Person-Year, 0.86/100 Person-Year & 7.18/100 Person-Year among IPT completed, in-completed and non-exposed patients, respectively. The adjusted Incidence Rate Ratio (aIRR) among IPT completed vs. non-exposed patients was 0.037 (95% CI, 0.016-0.072). Gender, residence area, employment status, baseline WHO stage of the disease (AIDS) and level of CD4 counts were identified as risk factors for TB incidence. The aIRR among patients who took Highly Active Anti- Retroviral Therapy (HAART) with IPT compared to those who took HAART alone was 0.063 (95% CI 0.035-0.104). IPT significantly reduced occurrence of active TB for 3 years.
IPT significantly reduced tuberculosis incidence by 96.3% compared to IPT non-exposed patients. Moreover concomitant use of HAART with IPT has shown a significant reduction in tuberculosis incidence by 93.7% than the use of HAART alone. Since IPT significantly protected occurrence of active TB for 3 years, its implementation should be further strengthened in the country.
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DOI: 10.1186/s12879-016-2109-7
PubMed: 28049455
PubMed Central: 5209939
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Effectiveness of isoniazid preventative therapy in reducing incidence of active tuberculosis among people living with HIV/AIDS in public health facilities of Addis Ababa, Ethiopia: a historical cohort study</title><author><name sortKey="Semu, Mahlet" sort="Semu, Mahlet" uniqKey="Semu M" first="Mahlet" last="Semu">Mahlet Semu</name><affiliation><nlm:aff id="Aff1">Addis Ababa Health Bureau, Addis Ababa, Ethiopia</nlm:aff></affiliation></author><author><name sortKey="Fenta, Teferi Gedif" sort="Fenta, Teferi Gedif" uniqKey="Fenta T" first="Teferi Gedif" last="Fenta">Teferi Gedif Fenta</name><affiliation><nlm:aff id="Aff2">Social and Administrative Pharmacy Working Group, Department of Pharmaceutics and Social Pharmacy, College of Health Sciences, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia</nlm:aff></affiliation></author><author><name sortKey="Medhin, Girmay" sort="Medhin, Girmay" uniqKey="Medhin G" first="Girmay" last="Medhin">Girmay Medhin</name><affiliation><nlm:aff id="Aff3">Aklilu Lemma Institute of Pathobiology, Addis Ababa University, Addis Ababa, Ethiopia</nlm:aff></affiliation></author><author><name sortKey="Assefa, Dawit" sort="Assefa, Dawit" uniqKey="Assefa D" first="Dawit" last="Assefa">Dawit Assefa</name><affiliation><nlm:aff id="Aff4">KNCV TB Care I-Ethiopia, Addis Ababa, Ethiopia</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">28049455</idno><idno type="pmc">5209939</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5209939</idno><idno type="RBID">PMC:5209939</idno><idno type="doi">10.1186/s12879-016-2109-7</idno><date when="2017">2017</date><idno type="wicri:Area/Pmc/Corpus">000622</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000622</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Effectiveness of isoniazid preventative therapy in reducing incidence of active tuberculosis among people living with HIV/AIDS in public health facilities of Addis Ababa, Ethiopia: a historical cohort study</title><author><name sortKey="Semu, Mahlet" sort="Semu, Mahlet" uniqKey="Semu M" first="Mahlet" last="Semu">Mahlet Semu</name><affiliation><nlm:aff id="Aff1">Addis Ababa Health Bureau, Addis Ababa, Ethiopia</nlm:aff></affiliation></author><author><name sortKey="Fenta, Teferi Gedif" sort="Fenta, Teferi Gedif" uniqKey="Fenta T" first="Teferi Gedif" last="Fenta">Teferi Gedif Fenta</name><affiliation><nlm:aff id="Aff2">Social and Administrative Pharmacy Working Group, Department of Pharmaceutics and Social Pharmacy, College of Health Sciences, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia</nlm:aff></affiliation></author><author><name sortKey="Medhin, Girmay" sort="Medhin, Girmay" uniqKey="Medhin G" first="Girmay" last="Medhin">Girmay Medhin</name><affiliation><nlm:aff id="Aff3">Aklilu Lemma Institute of Pathobiology, Addis Ababa University, Addis Ababa, Ethiopia</nlm:aff></affiliation></author><author><name sortKey="Assefa, Dawit" sort="Assefa, Dawit" uniqKey="Assefa D" first="Dawit" last="Assefa">Dawit Assefa</name><affiliation><nlm:aff id="Aff4">KNCV TB Care I-Ethiopia, Addis Ababa, Ethiopia</nlm:aff></affiliation></author></analytic><series><title level="j">BMC Infectious Diseases</title><idno type="eISSN">1471-2334</idno><imprint><date when="2017">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>Human Immunodeficiency Virus (HIV) pandemic has exacerbated tuberculosis disease especially in Sub-Saharan African countries. The World Health Organization (WHO) and Joint United Nations Program on HIV/AIDS (UNAIDS) have recommended Isoniazid Preventive Therapy (IPT) for HIV infected patients to reduce the burden of tuberculosis (TB). Ethiopia has been implementing IPT since 2007. However, effectiveness of IPT in averting occurrence of active tuberculosis among HIV infected patients has not been assessed.</p></sec><sec><title>Methods</title><p>Retrospective cohort study was employed using secondary data from public health institutions of Addis Ababa. Descriptive statistics and Generalized Linear Model based on Poisson regression was used for data analysis.</p></sec><sec><title>Results</title><p>From 2524 HIV infected patients who were followed for 4106 Person-Years, a total of 277 incident Tuberculosis (TB) cases occurred. TB Incidence Rate was 0.21/100 Person-Year, 0.86/100 Person-Year & 7.18/100 Person-Year among IPT completed, in-completed and non-exposed patients, respectively. The adjusted Incidence Rate Ratio (aIRR) among IPT completed vs. non-exposed patients was 0.037 (95% CI, 0.016-0.072). Gender, residence area, employment status, baseline WHO stage of the disease (AIDS) and level of CD4 counts were identified as risk factors for TB incidence. The aIRR among patients who took Highly Active Anti- Retroviral Therapy (HAART) with IPT compared to those who took HAART alone was 0.063 (95% CI 0.035-0.104). IPT significantly reduced occurrence of active TB for 3 years.</p></sec><sec><title>Conclusions</title><p>IPT significantly reduced tuberculosis incidence by 96.3% compared to IPT non-exposed patients. Moreover concomitant use of HAART with IPT has shown a significant reduction in tuberculosis incidence by 93.7% than the use of HAART alone. Since IPT significantly protected occurrence of active TB for 3 years, its implementation should be further strengthened in the country.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Friedland, G" uniqKey="Friedland G">G Friedland</name></author><author><name sortKey="Churchyard, Gj" uniqKey="Churchyard G">GJ Churchyard</name></author><author><name sortKey="Nardell, E" uniqKey="Nardell E">E Nardell</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Lawn, Sd" uniqKey="Lawn S">SD Lawn</name></author><author><name sortKey="Harries, Ad" uniqKey="Harries A">AD Harries</name></author><author><name sortKey="Anglaret, X" uniqKey="Anglaret X">X Anglaret</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Belew, D" uniqKey="Belew D">D Belew</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Vieira De Souza, Ct" uniqKey="Vieira De Souza C">CT Vieira de Souza</name></author><author><name sortKey="Hokerberg, Yhm" uniqKey="Hokerberg Y">YHM Hökerberg</name></author><author><name sortKey="Pacheco, Sjb" uniqKey="Pacheco S">SJB Pacheco</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Woldehanna, S" uniqKey="Woldehanna S">S Woldehanna</name></author><author><name sortKey="Volmink, J" uniqKey="Volmink J">J Volmink</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Fennera, L" uniqKey="Fennera L">L Fennera</name></author><author><name sortKey="Forstera, M" uniqKey="Forstera M">M Forstera</name></author><author><name sortKey="Boulleb, A" uniqKey="Boulleb A">A Boulleb</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Grant, Ad" uniqKey="Grant A">AD Grant</name></author><author><name sortKey="Charalambous, S" uniqKey="Charalambous S">S Charalambous</name></author><author><name sortKey="Fielding, Kl" uniqKey="Fielding K">KL Fielding</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Khawcharoenporn, T" uniqKey="Khawcharoenporn T">T Khawcharoenporn</name></author><author><name sortKey="Apisarnthanarak, A" uniqKey="Apisarnthanarak A">A Apisarnthanarak</name></author><author><name sortKey="Manosuthi, W" uniqKey="Manosuthi W">W Manosuthi</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Getahun, H" uniqKey="Getahun H">H Getahun</name></author><author><name sortKey="Gunneberg, C" uniqKey="Gunneberg C">C Gunneberg</name></author><author><name sortKey="Granich, R" uniqKey="Granich R">R Granich</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Golub, Ej" uniqKey="Golub E">EJ Golub</name></author><author><name sortKey="Pronyk, P" uniqKey="Pronyk P">P Pronyk</name></author><author><name sortKey="Mohapi, L" uniqKey="Mohapi L">L Mohapi</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">BMC Infect Dis</journal-id><journal-id journal-id-type="iso-abbrev">BMC Infect. Dis</journal-id><journal-title-group><journal-title>BMC Infectious Diseases</journal-title></journal-title-group><issn pub-type="epub">1471-2334</issn><publisher><publisher-name>BioMed Central</publisher-name><publisher-loc>London</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">28049455</article-id><article-id pub-id-type="pmc">5209939</article-id><article-id pub-id-type="publisher-id">2109</article-id><article-id pub-id-type="doi">10.1186/s12879-016-2109-7</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Effectiveness of isoniazid preventative therapy in reducing incidence of active tuberculosis among people living with HIV/AIDS in public health facilities of Addis Ababa, Ethiopia: a historical cohort study</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Semu</surname><given-names>Mahlet</given-names></name><address><email>mahletsemu@gmail.com</email></address><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author" corresp="yes"><name><surname>Fenta</surname><given-names>Teferi Gedif</given-names></name><address><phone>+251 911684854</phone><email>tgedif@gmail.com</email></address><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Medhin</surname><given-names>Girmay</given-names></name><address><email>gtmedhin@gmail.com</email></address><xref ref-type="aff" rid="Aff3">3</xref></contrib><contrib contrib-type="author"><name><surname>Assefa</surname><given-names>Dawit</given-names></name><address><email>Dawitaa11@yahoo.com</email></address><xref ref-type="aff" rid="Aff4">4</xref></contrib><aff id="Aff1"><label>1</label>Addis Ababa Health Bureau, Addis Ababa, Ethiopia</aff><aff id="Aff2"><label>2</label>Social and Administrative Pharmacy Working Group, Department of Pharmaceutics and Social Pharmacy, College of Health Sciences, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia</aff><aff id="Aff3"><label>3</label>Aklilu Lemma Institute of Pathobiology, Addis Ababa University, Addis Ababa, Ethiopia</aff><aff id="Aff4"><label>4</label>KNCV TB Care I-Ethiopia, Addis Ababa, Ethiopia</aff></contrib-group><pub-date pub-type="epub"><day>3</day><month>1</month><year>2017</year></pub-date><pub-date pub-type="pmc-release"><day>3</day><month>1</month><year>2017</year></pub-date><pub-date pub-type="collection"><year>2017</year></pub-date><volume>17</volume><elocation-id>5</elocation-id><history><date date-type="received"><day>19</day><month>4</month><year>2016</year></date><date date-type="accepted"><day>10</day><month>12</month><year>2016</year></date></history><permissions><copyright-statement>© The Author(s). 2017</copyright-statement><license license-type="OpenAccess"><license-p><bold>Open Access</bold>This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">http://creativecommons.org/publicdomain/zero/1.0/</ext-link>) applies to the data made available in this article, unless otherwise stated.</license-p></license></permissions><abstract id="Abs1"><sec><title>Background</title><p>Human Immunodeficiency Virus (HIV) pandemic has exacerbated tuberculosis disease especially in Sub-Saharan African countries. The World Health Organization (WHO) and Joint United Nations Program on HIV/AIDS (UNAIDS) have recommended Isoniazid Preventive Therapy (IPT) for HIV infected patients to reduce the burden of tuberculosis (TB). Ethiopia has been implementing IPT since 2007. However, effectiveness of IPT in averting occurrence of active tuberculosis among HIV infected patients has not been assessed.</p></sec><sec><title>Methods</title><p>Retrospective cohort study was employed using secondary data from public health institutions of Addis Ababa. Descriptive statistics and Generalized Linear Model based on Poisson regression was used for data analysis.</p></sec><sec><title>Results</title><p>From 2524 HIV infected patients who were followed for 4106 Person-Years, a total of 277 incident Tuberculosis (TB) cases occurred. TB Incidence Rate was 0.21/100 Person-Year, 0.86/100 Person-Year & 7.18/100 Person-Year among IPT completed, in-completed and non-exposed patients, respectively. The adjusted Incidence Rate Ratio (aIRR) among IPT completed vs. non-exposed patients was 0.037 (95% CI, 0.016-0.072). Gender, residence area, employment status, baseline WHO stage of the disease (AIDS) and level of CD4 counts were identified as risk factors for TB incidence. The aIRR among patients who took Highly Active Anti- Retroviral Therapy (HAART) with IPT compared to those who took HAART alone was 0.063 (95% CI 0.035-0.104). IPT significantly reduced occurrence of active TB for 3 years.</p></sec><sec><title>Conclusions</title><p>IPT significantly reduced tuberculosis incidence by 96.3% compared to IPT non-exposed patients. Moreover concomitant use of HAART with IPT has shown a significant reduction in tuberculosis incidence by 93.7% than the use of HAART alone. Since IPT significantly protected occurrence of active TB for 3 years, its implementation should be further strengthened in the country.</p></sec></abstract><kwd-group xml:lang="en"><title>Keywords</title><kwd>IPT</kwd><kwd>Incidence of active TB</kwd><kwd>TB/HIV co-infection</kwd><kwd>Ethiopia</kwd></kwd-group><funding-group><award-group><funding-source><institution>AAU Graduate Program and KNCV-TB Ethiopia</institution></funding-source></award-group></funding-group><custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name><meta-value>© The Author(s) 2017</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec id="Sec1"><title>Background</title><p>Tuberculosis (TB) and Human Immunodeficiency virus/Acquired Immunodeficiency Syndrome (HIV/AIDS) are major public health threat [<xref ref-type="bibr" rid="CR1">1</xref>–<xref ref-type="bibr" rid="CR3">3</xref>]. Among HIV infected patients, TB is the most frequent life threatening opportunistic disease, even in those receiving Highly Active Antiretroviral Therapy (HAART) and it has been shown to be a leading cause of death [<xref ref-type="bibr" rid="CR2">2</xref>, <xref ref-type="bibr" rid="CR4">4</xref>, <xref ref-type="bibr" rid="CR5">5</xref>]. HIV infection is also the strongest risk factor for TB disease [<xref ref-type="bibr" rid="CR3">3</xref>]. In 2011, globally there were 34 million HIV infected patients and at least one-third of these had latent TB & 1.1 million of them developed new TB infection, of these around 79% of patients were from Sub-Saharan African countries, indicating that HIV is fueling the TB epidemics in the region [<xref ref-type="bibr" rid="CR5">5</xref>]. In Ethiopia like many of the developing countries, TB has created major burden to the health care system due to its linkage with HIV/AIDS epidemics [<xref ref-type="bibr" rid="CR6">6</xref>]. In 2010, TB incidence in HIV-positive patients was 48 (27–76) per 100,000 population and the prevalence of TB including among HIV positives was 572(265–947) per 100,000 population [<xref ref-type="bibr" rid="CR7">7</xref>].</p><p>Since 1998, WHO and the Joint United Nations Program on HIV/AIDS (UNAIDS) have recommended Isoniazid Preventive Therapy (IPT) as one of the key interventions in the comprehensive HIV/AIDS care strategy to reduce the burden of TB among HIV infected patients [<xref ref-type="bibr" rid="CR8">8</xref>]. According to WHO [<xref ref-type="bibr" rid="CR2">2</xref>], IPT given to HIV infected patients without TB disease reduces the risk of developing TB by 33–67% for up to 48 months. Regarding the concomitant use of HAART with IPT, a meta-analysis led by WHO found out that HAART reduces the individual risk of TB disease by 65%, irrespective of the CD4 cell count but recent evidence has shown that the combined use of IPT and HAART among HIV infected patients significantly reduces the incidence of TB by up to 97% [<xref ref-type="bibr" rid="CR9">9</xref>].</p><p>In Ethiopia, IPT provision for HIV infected patients is recommended by the national TB/HIV Collaborative Activities guideline and its implementation has been started since 2007[<xref ref-type="bibr" rid="CR10">10</xref>]. However, the effectiveness of IPT in reducing the burden of active TB among HIV infected patients relative to those who did not take or discontinued has not been assessed yet. Moreover the clinical and programmatic factors affecting the treatment outcome among those who took have not been clearly identified. Therefore, this study assessed the effectiveness of the provision of IPT for HIV infected patients in averting occurrence of TB in the Ethiopian context.</p></sec><sec id="Sec2"><title>Methods</title><p>A multi-centered retrospective cohort study design was employed using secondary data from 14 public health facilities giving ART service in Addis Ababa. From seven facilities which were giving IPT service between 2007 and January 2010, all adult HIV positive patients (1264) who were either on HAART or Pre-ART and exposed to IPT in the study period and who were followed for at least a year were included as IPT exposed patients. All IPT discontinued patients regardless of their follow up time were also included. For comparison, equivalent number of non- IPT exposed patients who were on HIV care management for 1 or more years were sampled from randomly selected facilities which were not providing IPT till January 2010. All pediatric HIV positive patients regardless of whether they took/did not take IPT in the study period set, and all transferred in patients were excluded from this study. The patient charts from each facility were selected by random sampling method. A structured data abstraction format was used to collect information from medical records/chart of patients and the data was collected from July 1 to August 31, 2012. The data was entered and processed using SPSS version 16 statistical software. Descriptive statistics for patient characterization, Generalized Linear Model based on Poisson distribution to get incidence rate and incidence rate ratio, nonparametric test and Chi Square test were used for statistical analysis.</p></sec><sec id="Sec3"><title>Results</title><p>A total of 2528 patients’ charts were reviewed and four charts were with incomplete information and hence only 2524 charts were included in analysis. Of these, 1582(62.7%) were female and their mean age was 34.9 years. Majority were married and from Orthodox family. A significant proportion (44.9%) was un-employed. There is significant difference in level of education, marital status and employment status (Table <xref rid="Tab1" ref-type="table">1</xref>).<table-wrap id="Tab1"><label>Table 1</label><caption><p>Socio-demographic characteristics of patients at enrollment for chronic HIV care in public health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Socio-demographic profile at enrollment for HIV care (<italic>N</italic> = 2524)</th><th>IPT Exposed<break></break><italic>N</italic> (%)</th><th>IPT Non-exposed<break></break><italic>N</italic> (%)</th><th>Total<break></break><italic>N</italic> (%)</th><th>Chi-square<break></break><italic>P</italic> value</th></tr></thead><tbody><tr><td colspan="5">Sex</td></tr><tr><td> Male</td><td>473(37.4)</td><td>469(37.2)</td><td>942(37.3)</td><td>0.918</td></tr><tr><td> Female</td><td>791(62.6)</td><td>791(62.8)</td><td>1582(62.7)</td><td></td></tr><tr><td colspan="5">Age in years (mean = 34.9, SD = 9.1)</td></tr><tr><td> <30</td><td>421(33.3)</td><td>557(44.2)</td><td>978(38.7)</td><td>0.150</td></tr><tr><td> 30–39</td><td>408(32.3)</td><td>412(32.7)</td><td>820(32.5)</td><td></td></tr><tr><td> 40–49</td><td>283(22.4)</td><td>247(19.6)</td><td>530(21)</td><td></td></tr><tr><td> >50</td><td>152(12)</td><td>44(3.5)</td><td>196(7.8)</td><td></td></tr><tr><td colspan="5">Marital status</td></tr><tr><td> Single</td><td>318(25.2)</td><td>288(22.9)</td><td>606(24)</td><td>0.000</td></tr><tr><td> Married</td><td>584(46.2)</td><td>551(43.7)</td><td>1135(45)</td><td></td></tr><tr><td> Widowed</td><td>189(15)</td><td>195(15.5)</td><td>384(15.2)</td><td></td></tr><tr><td> Separated</td><td>157(12.4)</td><td>165(13.1)</td><td>322(12.8)</td><td></td></tr><tr><td> Divorced</td><td>16(1.3)</td><td>61(4.8)</td><td>77(3.1)</td><td></td></tr><tr><td colspan="5">Level of Education</td></tr><tr><td> No formal education</td><td>248(19.6)</td><td>276(21.9)</td><td>524(20.8)</td><td>0.004</td></tr><tr><td> Primary completed</td><td>507(40.1)</td><td>447(35.5)</td><td>954(37.8)</td><td></td></tr><tr><td> Secondary completed</td><td>473(37.4)</td><td>473(37.5)</td><td>946(37.5)</td><td></td></tr><tr><td> Tertiary completed</td><td>36(2.8)</td><td>64(5.1)</td><td>100(4)</td><td></td></tr><tr><td colspan="5">Religion</td></tr><tr><td> Orthodox</td><td>979(77.5)</td><td>1023(81.2)</td><td>2002(79.3)</td><td>0.197</td></tr><tr><td> Muslim</td><td>98(7.8)</td><td>177(14)</td><td>275(10.9)</td><td></td></tr><tr><td> Protestant</td><td>132(10.4)</td><td>54(4.3)</td><td>236(9.4)</td><td></td></tr><tr><td> Others<sup>a</sup></td><td>5(0.4)</td><td>6(0.5)</td><td>11(0.4)</td><td></td></tr><tr><td colspan="5">Employment status</td></tr><tr><td> Non-employed</td><td>650(51.4)</td><td>483(38.3)</td><td>1133(44.9)</td><td>0.000</td></tr><tr><td> Self-employed</td><td>218(17.2)</td><td>247(19.6)</td><td>465(18.4)</td><td></td></tr><tr><td> Government employed</td><td>205(16.2)</td><td>248(19.7)</td><td>453(17.95)</td><td></td></tr><tr><td> Private</td><td>183(14.5)</td><td>270(21.4)</td><td>453(17.95)</td><td></td></tr><tr><td> Student</td><td>8(0.63)</td><td>12(0.95)</td><td>20(0.8)</td><td></td></tr><tr><td colspan="5">Residence place</td></tr><tr><td> Addis Ababa</td><td>1230(97.3)</td><td>1252(99.4)</td><td>2482(98.3)</td><td>0.322</td></tr><tr><td> Out of Addis Ababa</td><td>34(2.7)</td><td>8(0.6)</td><td>42(1.7)</td><td></td></tr><tr><td>Average no. of personnel per family</td><td>3.15</td><td>3.45</td><td>3.3</td><td>0.092</td></tr><tr><td>Average no. of rooms per family</td><td>1.35</td><td>1.65</td><td>1.5</td><td>0.593</td></tr></tbody></table><table-wrap-foot><p><sup>a</sup>Catholic and Joba</p></table-wrap-foot></table-wrap></p><p>All of the patients were Pre-ART at the time of enrollment for chronic HIV care and the baseline clinical information of the patients is shown in Table <xref rid="Tab2" ref-type="table">2</xref>. Majority of the patients were in stage 3 followed by stage 2, 972 (38.5%) and 833 (33%), respectively. There was significant clinical difference between the two groups.<table-wrap id="Tab2"><label>Table 2</label><caption><p>Baseline clinical information of HIV positive patients in public health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Baseline Clinical status (<italic>N</italic> = 2524)</th><th>IPT Exposed<break></break><italic>N</italic> (%)</th><th>IPT Non-exposed<break></break><italic>N</italic> (%)</th><th>Total<break></break><italic>N</italic> (%)</th><th>Chi-square<break></break><italic>P</italic> value</th></tr></thead><tbody><tr><td colspan="5">Initial WHO stage of HIV/AIDS</td></tr><tr><td> Stage 1</td><td>357(28.2)</td><td>215(17.1)</td><td>572(22.7)</td><td>0.000</td></tr><tr><td> Stage 2</td><td>487(38.5)</td><td>346(27.5)</td><td>833(33)</td><td></td></tr><tr><td> Stage 3</td><td>392(31)</td><td>580(46)</td><td>972(38.5)</td><td></td></tr><tr><td> Stage 4</td><td>28(2.3)</td><td>119(9.4)</td><td>147(5.8)</td><td></td></tr><tr><td colspan="5">Baseline CD<sub>4</sub>cells count/μl(mean = 230, SD = 176.9)</td></tr><tr><td> ≤200</td><td>570(45.1)</td><td>807(64)</td><td>1377(54.6)</td><td>0.000</td></tr><tr><td> >200</td><td>694(54.9)</td><td>453(36)</td><td>1147(45.4)</td><td></td></tr><tr><td colspan="5">Initial body weight in Kg (mean = 53.8, SD = 9.7)</td></tr><tr><td> <50</td><td>304(24.1)</td><td>554(43.8)</td><td>858(34)</td><td>0.009</td></tr><tr><td> 50–59</td><td>628(49.7)</td><td>418(33.1)</td><td>1046(41.4)</td><td></td></tr><tr><td> 60–69</td><td>208(16.5)</td><td>214(17)</td><td>422(16.7)</td><td></td></tr><tr><td> >69</td><td>124(9.8)</td><td>74(5.9)</td><td>198(7.8)</td><td></td></tr><tr><td colspan="5">TB screened<sup>a</sup></td></tr><tr><td> Positive</td><td>0</td><td>40(3.2)</td><td>40(1.6)</td><td></td></tr><tr><td> Negative</td><td>1264(100)</td><td>1220(96.8)</td><td>2484(98.4)</td><td></td></tr><tr><td colspan="5"> On CPT</td></tr><tr><td> Yes</td><td>1259(99.6)</td><td>1205(95.6)</td><td>2464(97.6)</td><td>0.000</td></tr><tr><td> No</td><td>5(0.4)</td><td>55(4.4)</td><td>60(2.4)</td><td></td></tr><tr><td colspan="5">OIs diagnosed</td></tr><tr><td> None</td><td>1082(85.6)</td><td>907(71.9)</td><td>1989(78.8)</td><td>0.000</td></tr><tr><td> Bacterial infections</td><td>11(0.87)</td><td>164(13)</td><td>175(6.9)</td><td></td></tr><tr><td> Viral infections</td><td>25(0.08)</td><td>88(6.9)</td><td>113(4.5)</td><td></td></tr><tr><td> Fungal infections</td><td>38(3)</td><td>129(10.2)</td><td>167(6.6)</td><td></td></tr><tr><td> Viral & bacterial infections</td><td>20(1.6)</td><td>13(1.03)</td><td>33(1.3)</td><td></td></tr><tr><td> Bacterial & fungal infections</td><td>11(0.87)</td><td>8(0.63)</td><td>19(0.8)</td><td></td></tr><tr><td> Fungal & viral infections</td><td>8(0.6)</td><td>12(0.95)</td><td>20(0.8)</td><td></td></tr></tbody></table><table-wrap-foot><p><sup>a</sup>A patient is TB positive, if he/she has at least two of these signs/symptoms: Weight loss greater than or equal to 5% of the initial weight, coughing for 2 weeks, night sweat, night-mar, Loss of appetite</p></table-wrap-foot></table-wrap></p><p>As shown in Table <xref rid="Tab3" ref-type="table">3</xref>, from all patients for whom their charts were reviewed, 2046 (81.1%) had initiated HAART during their follow up; of whom 945 (46.2%) of them were WHO stage 3.<table-wrap id="Tab3"><label>Table 3</label><caption><p>Clinical information of patients who were unheard follow upinpublic health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Clinical information when ART initiated (<italic>N</italic> = 2046)</th><th>IPT exposed<break></break><italic>N</italic> (%)</th><th>IPT Non-exposed<break></break><italic>N</italic> (%)</th><th><italic>N</italic> (%)</th><th>Chi-square<break></break><italic>P</italic> value</th></tr></thead><tbody><tr><td colspan="5">WHO stage of HIV/AIDS</td></tr><tr><td> Stage 1</td><td>151(16.02)</td><td>138(12.5)</td><td>289(14.1)</td><td>0.000</td></tr><tr><td> Stage 2</td><td>367(39)</td><td>294(26.6)</td><td>661(32.3)</td><td></td></tr><tr><td> Stage 3</td><td>394 (41.8)</td><td>551(49.9)</td><td>945(46.2)</td><td></td></tr><tr><td> Stage 4</td><td>30 (3.18)</td><td>121(11.0)</td><td>151(7.4)</td><td></td></tr><tr><td colspan="5">CD<sub>4</sub>cells count/μl(mean = 151.2, SD = 84.9)</td></tr><tr><td> ≤200</td><td>537 (37.9)</td><td>1020(92.4)</td><td>1557(76.1)</td><td>0.000</td></tr><tr><td> >200</td><td>263 (27.9)</td><td>226(20.5)</td><td>489(23.9)</td><td></td></tr><tr><td colspan="5">Weight in Kg (mean = 53.2, SD = 9.5)</td></tr><tr><td> <50</td><td>241(25.6)</td><td>506(45.8)</td><td>747(36.5)</td><td>0.011</td></tr><tr><td> 50–59</td><td>479(44.2)</td><td>366(33.1)</td><td>845(41.3)</td><td></td></tr><tr><td> 60–69</td><td>164 (17.4)</td><td>164(14.9)</td><td>328(16.0)</td><td></td></tr><tr><td> >69</td><td>58 (6.2)</td><td>68(6.2)</td><td>126(6.2)</td><td></td></tr><tr><td colspan="5">TB screened</td></tr><tr><td> Yes</td><td>942(100)</td><td>1100(99.6)</td><td>2042(99.8)</td><td>0.64</td></tr><tr><td> No</td><td>0</td><td>4(0.4)</td><td>4(0.2)</td><td></td></tr><tr><td colspan="5">CPT adherence</td></tr><tr><td> Good</td><td>791(84)</td><td>1096(99.3)</td><td>2032(99.6)</td><td>0.046</td></tr><tr><td> Fair</td><td>3(.32)</td><td>6(0.5)</td><td>9(0.3)</td><td></td></tr><tr><td> Poor</td><td>3(.32)</td><td>2(0.2)</td><td>5(0.2)</td><td></td></tr><tr><td colspan="5">ART adherence</td></tr><tr><td> Good</td><td>937(99.5)</td><td>1100(99.6)</td><td>2037(99.6)</td><td>0.124</td></tr><tr><td> Fair</td><td>5(0.53)</td><td>2(0.2)</td><td>7(0.3)</td><td></td></tr><tr><td> Poor</td><td>0</td><td>2(0.2)</td><td>2(0.1)</td><td></td></tr><tr><td colspan="5">OIs after ART initiated</td></tr><tr><td> None</td><td>937(99.5)</td><td>1052(95.3)</td><td>1989(97.21)</td><td>0.000</td></tr><tr><td> Fungal</td><td>3(.32)</td><td>20(1.8)</td><td>23(1.12)</td><td></td></tr><tr><td> Viral</td><td>0</td><td>12(1.0)</td><td>12(0.5)</td><td></td></tr><tr><td> Bacterial</td><td>0</td><td>12(1.0)</td><td>14(0.7)</td><td></td></tr><tr><td> Bacterial & fungal</td><td>0</td><td>4(0.4)</td><td>4(0.2)</td><td></td></tr><tr><td> Others<sup>a</sup></td><td>0</td><td>4(0.4)</td><td>4(0.2)</td><td></td></tr></tbody></table><table-wrap-foot><p><sup>a</sup>Protozoal, viral & bacterial & fungal & viral infections</p></table-wrap-foot></table-wrap></p><p>Out of 1264 patients who were given IPT, completion rate was 975(77.1%). Among IPT exposed patients; 942(74.5%) were on HAART and of these 738(78.3%) completed IPT (Table <xref rid="Tab4" ref-type="table">4</xref>).<table-wrap id="Tab4"><label>Table 4</label><caption><p>Profile of IPT exposed patients inpublic health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Profile (<italic>N</italic> = 1264)</th><th><italic>N</italic> (%)</th><th>Chi-square<break></break><italic>P</italic>-value</th></tr></thead><tbody><tr><td> Male</td><td>473(37.4%)</td><td></td></tr><tr><td> Female</td><td>791(62.6%)</td><td></td></tr><tr><td>TB screened & tested negative</td><td>1264(100%)</td><td></td></tr><tr><td>Currently on HAART</td><td>942(74.5%)</td><td></td></tr><tr><td>Pre-ART</td><td>322(25.5%)</td><td></td></tr><tr><td>HAART initiated before IPT</td><td>578(61.3%)</td><td></td></tr><tr><td>HAART initiated after IPT</td><td>364(38.7%)</td><td></td></tr><tr><td>IPT completed</td><td>975(77.1%)</td><td></td></tr><tr><td>IPT discontinued</td><td>289(22.9%)</td><td></td></tr><tr><td>On HAART + IPT completed</td><td>738(78.3%)</td><td rowspan="2">0.094</td></tr><tr><td>Pre-ART + IPT completed</td><td>237(73.6%)</td></tr><tr><td>On HAART + IPT in-completed</td><td>204(21.7%)</td><td>0.08</td></tr><tr><td>Pre-ART + IPT in-completed</td><td>85(26.4%)</td><td></td></tr><tr><td>Male IPT completed</td><td>359(75.9%)</td><td rowspan="2">0.459</td></tr><tr><td>Female IPT completed</td><td>616(77.8%)</td></tr><tr><td>Took B<sub>6</sub> together with INH</td><td>581(46%)</td><td></td></tr><tr><td>No IPT side effects</td><td>1254(99.2%)</td><td></td></tr></tbody></table></table-wrap></p><p>Among 2524 HIV-infected patients who were followed for 4106 P-Y, 277 incident TB cases occurred, making the overall incidence of 6.7/100P-Y. Among IPT completed group, incidence rate was 0.21/100PY, while in IPT non-exposed patients; it was 7.18/100P-Y. Incidence of TB was found to be associated with sex, employment status, baseline WHO stage of HIV/AIDS and CD<sub>4</sub> count. Completion of IPT showed significant protective effect against occurrence of active TB when compared to IPT non-exposed patients aIRR = 0.037 (CI 95% 0.016-0.072)} (Table <xref rid="Tab5" ref-type="table">5</xref>, Fig. <xref rid="Fig1" ref-type="fig">1</xref>).<table-wrap id="Tab5"><label>Table 5</label><caption><p>Incidence rate, univariate and multivariate analysis among IPT completed, in-completed and non- exposed patients in public health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Patient profile</th><th>Event/P/Y</th><th>IR/100P-Y</th><th>Crude IRR (95% CI)</th><th>Adjusted IRR(95% CI)</th></tr></thead><tbody><tr><td>Over all</td><td>277/4106</td><td>6.7</td><td></td><td></td></tr><tr><td>IPT completed</td><td>7/33.3</td><td>0.21</td><td>0.03(0.01–0.06)</td><td>0.04(0.05–0.07)</td></tr><tr><td>IPT in-completed</td><td>8/7.8</td><td>0.86</td><td>0.84(0.36–1.33)</td><td>0.89(0.49–1.76)</td></tr><tr><td>IPT non-exposed</td><td>262/36.49</td><td>7.18</td><td>1</td><td>1</td></tr><tr><td colspan="5">Sex</td></tr><tr><td> Male</td><td>138/2822.1</td><td>4.89</td><td>1.80(1.42–2.28)</td><td>1.59(1.20–2.12)</td></tr><tr><td> Female</td><td>139/5129.2</td><td>2.71</td><td>1</td><td>1</td></tr><tr><td colspan="5">Age group in year</td></tr><tr><td> <30</td><td>103/3038.3</td><td>3.39</td><td>1</td><td>1</td></tr><tr><td> 30–39</td><td>87/2628.4</td><td>3.31</td><td>0.98(0.73–1.29)</td><td>0.82(0.61–1.11)</td></tr><tr><td> 40–49</td><td>61/1644.2</td><td>3.71</td><td>1.09(0.79–1.49)</td><td>1.04(0.74–1.47)</td></tr><tr><td> >49</td><td>26/637.3</td><td>4.08</td><td>1.201(0.77–1.82)</td><td>1.55(0.95–2.44)</td></tr><tr><td colspan="5">Residence area</td></tr><tr><td> Living out of Addis Ababa</td><td>4/135.1</td><td>2.96</td><td>0.85(0.26–1.99)</td><td>0.29(0.09–0.73)</td></tr><tr><td> Living in Addis Ababa</td><td>273/7800</td><td>3.50</td><td>1</td><td>1</td></tr><tr><td colspan="5">Religion</td></tr><tr><td> Orthodox</td><td>231/6243.2</td><td>3.70</td><td>0.63(0.20–3.82)</td><td>0.29(0.08–1.86)</td></tr><tr><td> Muslim</td><td>19/892</td><td>2.13</td><td>0.36(0.11–2.28)</td><td>0.17(0.04–1.13)</td></tr><tr><td> Protestant</td><td>25/778.8</td><td>3.21</td><td>0.55(0.16–3.40)</td><td>0.32(0.09–2.12)</td></tr><tr><td> Others*</td><td>11/187.7</td><td>5.86</td><td>1</td><td>1</td></tr><tr><td colspan="5">Marital status</td></tr><tr><td> Married</td><td>127/3547.5</td><td>3.58</td><td>0.82(0.46–1.68)</td><td>1.22(0.66–2.51)</td></tr><tr><td> Single</td><td>72/1889.8</td><td>3.81</td><td>0.88(0.48–1.81)</td><td>1.18(0.63–2.48)</td></tr><tr><td> Widowed</td><td>33/1284</td><td>2.57</td><td>0.59(0.30–1.27)</td><td>0.81(0.40–1.76)</td></tr><tr><td> Divorced</td><td>35/997.2</td><td>3.51</td><td>0.81(0.45–1.72)</td><td>1.05(0.53–2.27)</td></tr><tr><td> Separated</td><td>10/229.9</td><td>4.35</td><td>1</td><td>1</td></tr><tr><td colspan="5">Employment</td></tr><tr><td> Self employed</td><td>87/3782.6</td><td>2.30</td><td>0.03(0.01–0.19)</td><td>0.02(0.01–0.12)</td></tr><tr><td> Private Employed</td><td>58/1418.1</td><td>4.09</td><td>0.06(0.02–0.35)</td><td>0.03(0.01–0.16)</td></tr><tr><td> Government employed</td><td>62/1324.8</td><td>4.68</td><td>0.07(0.02–0.40)</td><td>0.03(0.01–0.19)</td></tr><tr><td> Student</td><td>3/66.5</td><td>4.51</td><td>0.06(0.01–0.48)</td><td>0.01(0.002–0.101)</td></tr><tr><td> Non- employed</td><td>65/1354.2</td><td>4.80</td><td>1</td><td>1</td></tr><tr><td colspan="5">Educational level</td></tr><tr><td> None educated</td><td>42/1707.3</td><td>2.46</td><td>0.65(0.35–1.33)</td><td>1.25(0.62–2.70)</td></tr><tr><td> Primary Completed</td><td>106/3028.6</td><td>3.50</td><td>0.93(0.52–1.83)</td><td>1.69(0.89–3.49)</td></tr><tr><td> Secondary Completed</td><td>118/2920.8</td><td>4.04</td><td>1.07(0.60–2.10)</td><td>1.76(0.97–3.55)</td></tr><tr><td> Tertiary completed</td><td>11/291</td><td>3.78</td><td>1</td><td>1</td></tr><tr><td>House Hold size/room no.</td><td></td><td></td><td>0.99(0.89–1.09)</td><td>0.98(0.88–1.07)</td></tr><tr><td colspan="5">Baseline WHO stage of HIV/AIDS</td></tr><tr><td> Stage 1 & 2</td><td>45/4545.5</td><td>0.99</td><td>0.14(0.10–0.19)</td><td>0.23(0.16–0.31)</td></tr><tr><td> Stage 3 & 4</td><td>232/3381.9</td><td>6.86</td><td></td><td>1</td></tr><tr><td>Baseline CD<sub>4</sub> cells/μl</td><td></td><td></td><td></td><td></td></tr><tr><td> ≤200</td><td>211/4169.9</td><td>5.06</td><td>2.89(2.21–3.85)</td><td>1.36(1.02–1.84)</td></tr><tr><td> >200</td><td>66/3771.4</td><td>1.75</td><td></td><td></td></tr><tr><td colspan="5">Baseline weight in Kg</td></tr><tr><td> ≤49</td><td>113/2646.4</td><td>4.27</td><td>1.88(1.12–3.43)</td><td>1.63(0.93–3.05)</td></tr><tr><td> 50–59</td><td>108/3343.7</td><td>3.23</td><td>1.42(0.85–2.59)</td><td>1.19(0.69–2.22)</td></tr><tr><td> 60–69</td><td>42/1333.3</td><td>3.15</td><td>1.39(0.78–2.64)</td><td>1.06(0.59–2.03)</td></tr><tr><td> >69</td><td>14/616.7</td><td>2.27</td><td>1</td><td>1</td></tr><tr><td colspan="5">Baseline OIs</td></tr><tr><td> Yes</td><td>194/6278.3</td><td>3.09</td><td>0.62(0.48–0.80)</td><td>1.24(0.95–1.63)</td></tr><tr><td> No</td><td>83/1660</td><td>5.00</td><td>1</td><td>1</td></tr><tr><td>CPT adherence</td><td></td><td></td><td></td><td></td></tr><tr><td> Good</td><td>271/7765</td><td>3.49</td><td>0.99(0.48–2.51)</td><td>0.92(0.44–2.37)</td></tr><tr><td> Fair, Poor & no CPT</td><td>2/56.8</td><td>3.52</td><td>1</td><td>1</td></tr></tbody></table><table-wrap-foot><p>*others include: catholic, johoba and non belivers</p></table-wrap-foot></table-wrap><fig id="Fig1"><label>Fig. 1</label><caption><p>Incidence rate among IPT completed, in-completed and non- exposed patientsin public health facilities of Addis Ababa, during 2007-June 2012</p></caption><graphic xlink:href="12879_2016_2109_Fig1_HTML" id="MO1"></graphic></fig></p><p>Similarly, as shown in Table <xref rid="Tab6" ref-type="table">6</xref> and Fig. <xref rid="Fig2" ref-type="fig">2</xref>, those patients who took IPT with HAART had TB incidence rate of 0.42/100P-Y and among patients who took HAART alone, the incidence was 7.83/100P-Y. The concomitant use of IPT with HAART revealed significant protective effect on occurrence of active TB compared to HAART alone {aIRR =0.063(95% CI 0.035-0.104). Among IPT exposed patients, those who took IPT with HAART had lesser incidence than those who took IPT before initiating HAART {aIRR = 0.158(95% CI 0.039- 0.555)}.<table-wrap id="Tab6"><label>Table 6</label><caption><p>IR & IRR among patients who took HAART with or without IPT in public health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Therapy (<italic>N</italic> = 1842)</th><th>IR/100P-Y</th><th>aIRR(95% CI)</th></tr></thead><tbody><tr><td> IPT with HAART</td><td>0.42</td><td>0.063(0.035–0.104)</td></tr><tr><td> HAART only</td><td>7.83</td><td>1</td></tr><tr><td colspan="3">IPT initiation time with HAART</td></tr><tr><td> Took IPT with HAART</td><td>0.2</td><td>0.158(0.039–0.555)</td></tr><tr><td> Took IPT before initiating HAART</td><td>0.75</td><td>1</td></tr></tbody></table></table-wrap><fig id="Fig2"><label>Fig. 2</label><caption><p>IR among patients who took HAART with IPT in public health facilities of Addis Ababa, during 2007-June 2012</p></caption><graphic xlink:href="12879_2016_2109_Fig2_HTML" id="MO2"></graphic></fig></p><p>As shown in Table <xref rid="Tab7" ref-type="table">7</xref>, there was significant CD4 and weight changes among IPT-HAART treated patients.<table-wrap id="Tab7"><label>Table 7</label><caption><p>Statistical analysis of clinical data among patients who took HAART with IPT in public health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th colspan="2">Variables</th><th><italic>N</italic></th><th>Mean Rank</th><th><italic>P</italic>- value</th></tr></thead><tbody><tr><td rowspan="4">Weight after completing IPT – weight at enrollment</td><td>Negative Ranks</td><td>160<sup>a</sup></td><td>410.64</td><td></td></tr><tr><td>Positive Ranks</td><td>701<sup>b</sup></td><td>435.65</td><td>0.000</td></tr><tr><td>Ties</td><td>114<sup>c</sup></td><td></td><td></td></tr><tr><td>Total</td><td>975</td><td></td><td></td></tr><tr><td rowspan="4">CD4 after completing IPT - CD4 at enrollment</td><td>Negative Ranks</td><td>253<sup>d</sup></td><td>546.73</td><td></td></tr><tr><td>Positive Ranks</td><td>702<sup>e</sup></td><td>453.23</td><td>0.000</td></tr><tr><td>Ties</td><td>21<sup>f</sup></td><td></td><td></td></tr><tr><td>Total</td><td>976</td><td></td><td></td></tr></tbody></table><table-wrap-foot><p><sup>a</sup>Weight when completing IPT < weight when starting IPT</p><p><sup>b</sup>Weight when completing IPT > weight when starting IPT</p><p><sup>c</sup>Weight when completing IPT = weight when starting IPT</p><p><sup>d</sup>CD4 when completing IPT < CD4 when starting IPT</p><p><sup>e</sup>CD4 when completing IPT > CD4 when starting IPT</p><p><sup>f</sup>CD4 when completing IPT = CD4 when starting IPT</p></table-wrap-foot></table-wrap></p><p>The median duration of follow- up was 40 months (inter-quartile range, 28–52 months). From those who completed IPT, active TB has occurred between 6 and 28 months duration. Almost 50% of patients who completed IPT developed active TB at 19<sup>th</sup>month; while in non-exposed patients TB occurred within a month time of enrollment (Table <xref rid="Tab8" ref-type="table">8</xref>).<table-wrap id="Tab8"><label>Table 8</label><caption><p>Month of occurrence of active TB among IPT completed, in-completed & non-exposed patients in public health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Variables</th><th>No of patients active TB diagnosed</th><th>Minimum month TB occurred</th><th>Maximum month TB occurred</th><th>Mean month TB occurred</th><th>Standard Deviation</th><th>Median</th></tr></thead><tbody><tr><td>Month TB occurred among IPT completed patients</td><td>7</td><td>6</td><td>28</td><td char="." align="char">16.7</td><td char="." align="char">8.4</td><td>19</td></tr><tr><td>Month TB occurred among patients who discontinued IPT</td><td>8</td><td>0</td><td>35</td><td char="." align="char">9.6</td><td char="." align="char">14.8</td><td>0</td></tr><tr><td>Month TB occurred among IPT non-exposed</td><td>262</td><td>0</td><td>65</td><td char="." align="char">8.1</td><td char="." align="char">13.3</td><td>1</td></tr></tbody></table></table-wrap></p><p>As shown in Table <xref rid="Tab9" ref-type="table">9</xref>, IPT completers were significantly protected for 3 years {aIRR = 0.04 (95% CI (0.02-1.74)} compared to IPT in-completed and non-exposed patients.<table-wrap id="Tab9"><label>Table 9</label><caption><p>TB incidence in month interval among IPT completed, in-completed & non-exposed patients in public health facilities of Addis Ababa, during 2007-June 2012</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Follow up month</th><th>IPT exposure/completion status</th><th>IR/100 P-M (95% CI)</th><th>Unadjusted IRR (95% CI)</th><th>Adjusted IRR (95% CI)</th></tr></thead><tbody><tr><td rowspan="3"><6</td><td>Completed</td><td>0</td><td>0</td><td>0</td></tr><tr><td>In-complete</td><td>142.8(17.64–268.07)</td><td>1.82(0.65–3.97)</td><td>2.125(0.712–5.103)</td></tr><tr><td>Non-exposed</td><td>78.59(66.9–90.3)</td><td>1</td><td>1</td></tr><tr><td rowspan="3">6–12</td><td>Completed</td><td>12(1.58–25.58)</td><td>0.30(0.06–0.79)</td><td>0.03(0.013–1.95)</td></tr><tr><td>In-completed</td><td>38.71(7.74–69.68)</td><td>0.98(0.39–2.02)</td><td>1.05(0.32–2.89)</td></tr><tr><td>Non-exposed</td><td>39.43(34.05–44.82)</td><td>1</td><td>1</td></tr><tr><td rowspan="3">12–24</td><td>Completed</td><td>6.74(1.35–12.14)</td><td>0.29(0.11–0.59)</td><td>0.03(0.01–0.74)</td></tr><tr><td>In-completed</td><td>38.71(7.74–69.68)</td><td>1.65(0.65–3.38)</td><td>1.61(0.51–4.29)</td></tr><tr><td>Non-exposed</td><td>23.51(20.48–26.55)</td><td>1</td><td>1</td></tr><tr><td rowspan="3">24–36</td><td>Completed</td><td>5.98(1.55–10.42)</td><td>0.34(0.14–0.66)</td><td>0.04(0.02–1.74)</td></tr><tr><td>In-completed</td><td>9.94(3.05–16.82)</td><td>0.56(0.25–1.05)</td><td>1.09(0.49–2.54)</td></tr><tr><td>Non-exposed</td><td>17.87(15.63–20.11)</td><td>1</td><td>1</td></tr><tr><td rowspan="3">37–48</td><td>Completed</td><td>5.98(1.55–10.42)</td><td>0.44(0.186–0.854)</td><td>0.74(0.301–1.56)</td></tr><tr><td>In-completed</td><td>9.94(3.05–16.82)</td><td>0.73(0.33–1.37)</td><td>0.72(0.314–1.44)</td></tr><tr><td>Non-exposed</td><td>13.72(12.04–19.56</td><td>1</td><td>1</td></tr><tr><td rowspan="3">>48</td><td>Completed</td><td>5.98(1.55–10.42)</td><td>0.50(0.22–0.99)</td><td>0.88(0.36–1.84)</td></tr><tr><td>In-completed</td><td>9.94(3.05–16.82)</td><td>0.84(0.38–1.58)</td><td>0.89(0.39–1.76)</td></tr><tr><td>Non-exposed</td><td>11.88(10.44–13.32)</td><td>1</td><td>1</td></tr></tbody></table></table-wrap></p></sec><sec id="Sec4"><title>Discussion</title><p>This retrospective cohort study covering the time from 2007 to June 2012 attempted to assess effectiveness of IPT against active TB in HIV positive adults who were on HIV care in government health facilities of Addis Ababa. Accordingly, the IRs were 0.21/100P-Y, 0.86/100P-Y & 7.18/100P-Y among IPT completed, in-completed & non-exposed patients, respectively. The IR among IPT completed patients was lower when compared with the findings of studies done in different countries [<xref ref-type="bibr" rid="CR11">11</xref>–<xref ref-type="bibr" rid="CR13">13</xref>]. Moreover, completion of IPT in HIV infected adults significantly reduced TB incidence by 96.3% when compared to non-exposed patients (aIRR = 0.037, 95% CI 0.016-0.072). The present study revealed abetter reduction in TB incidence after IPT in comparison with the results of earlier studies [<xref ref-type="bibr" rid="CR7">7</xref>, <xref ref-type="bibr" rid="CR14">14</xref>–<xref ref-type="bibr" rid="CR16">16</xref>]. Better patient adherence rate, difference in TB burden among the countries or better socioeconomic and clinical status of patients might have contributed to such differences among studies conducted in different countries. Despite the fact that Ethiopia is among high TB burden country, IR among IPT completed patients was comparably lower than studies indicating further the effectiveness of IPT for HIV infected patients. Hence more widespread provision of IPT has the potential to further reduce TB incidence and hence improve quality of life among HIV infected adults in the country.</p><p>Among patients who completed IPT, though TB had occurred after 6 months, almost 50% of them developed TB at 19<sup>th</sup>month; while in IPT non-exposed patients, half of patients developed active TB within a month time. The study proved that IPT has been significantly protecting early occurrence of TB during the first 6 months. This finding was comparable to the study done in Thailand where IR among IPT completers was 0 and among non-exposed patients 8.60/100 P-Y [<xref ref-type="bibr" rid="CR17">17</xref>]. Moreover, the present study indicated that IPT had offered a significant protective effect until 3 years. The durability of protective effect of IPT documented in the present study concurs with the expected level indicated in Ethiopian guideline [<xref ref-type="bibr" rid="CR10">10</xref>]. It is, however, better than reports from South East Asian and other Sub-Saharan African countries [<xref ref-type="bibr" rid="CR13">13</xref>, <xref ref-type="bibr" rid="CR17">17</xref>, <xref ref-type="bibr" rid="CR18">18</xref>].</p><p>With regard to risk factors associated with TB occurrence, even though there is significant difference among the two groups in socio-demographic and baseline clinical characteristics, the multivariable analysis revealed significant influence of IPT completion, male sex, employment status, baseline WHO stage of HIV/AIDS (stage 3 & 4) & CD<sub>4</sub> cell count (less than 200cells/μl).</p><p>Similarly, South African and Namibian studies indicated the influence of clinical factors on the incidence of Tb among HIV patients [<xref ref-type="bibr" rid="CR13">13</xref>, <xref ref-type="bibr" rid="CR16">16</xref>].</p><p>Getahun et al. [<xref ref-type="bibr" rid="CR19">19</xref>] reported that in countries with a high prevalence of HIV, more women than men are diagnosed with TB. But the current study revealed that more males who took IPT were at risk of developing active TB than females (aIRR = 1.596(95% CI = 1.203-2.117). This was in agreement with the report made by Golub et al. [<xref ref-type="bibr" rid="CR20">20</xref>].</p><p>Concerning IPT initiation time with HAART, among IPT exposed patients; those patients who took IPT with HAART had 84.2% incidence reduction than those who took IPT prior to initiating HAART. This study also noted that there was significant CD<sub>4</sub>cell count and weight changes after taking IPT-HAART combination therapy compared to cell count at enrollment, which might have contributed for preventing TB recurrence. This finding could serve as a base for further studies to reach an understanding on whether concomitant initiation of IPT with HAART or delayed initiation of IPT is better in terms of efficacy, toxicity or the development of immune reconstitution. In general the current finding encourages further implementation of the therapy in the country so as to decrease the burden of TB among HIV infected patients.</p></sec><sec id="Sec5"><title>Conclusions</title><p>Completion of IPT significantly reduced TB incidence by 96.3% and IPT had significantly protected occurrence of active TB for three years among HIV infected patients. Male sex, CD<sub>4</sub> cell count less than 200cells/μl, WHO stage of HIV/AIDS 3 & 4 and being non-employed were risk factors for TB incidence. Concomitant use of HAART with IPT significantly decreased TB incidence by 93.7% more than HAART alone. This result evidenced and supported the WHO recommendations that IPT protected the occurrence of active TB and proved the effectiveness of IPT in reducing TB incidence among HIV infected patients in Ethiopia. Therefore, it should be implemented widely for HIV-infected patients in all parts of the country so as to improve their quality of life by reducing the TB burden and prevent further transmission of TB in the community.</p></sec></body><back><glossary><title>Abbreviations</title><def-list><def-item><term>IPT</term><def><p>Isoniazid preventive therapy</p></def></def-item><def-item><term>aIRR</term><def><p>Adjusted incidence rate ratio</p></def></def-item><def-item><term>HAART</term><def><p>Highly active antiretroviral therapy</p></def></def-item><def-item><term>IR</term><def><p>Incidence ratio</p></def></def-item><def-item><term>PMTCT</term><def><p>Prevention of mothers to child transmission of HIV</p></def></def-item><def-item><term>TB</term><def><p>Tuberculosis</p></def></def-item><def-item><term>WHO</term><def><p>World Health Organization</p></def></def-item><def-item><term>UNAIDS</term><def><p>United Nation programs on HIV/AIDS</p></def></def-item></def-list></glossary><ack><p>Special thanks go to Addis Ababa University, Graduate Study Program and KNCV TB Care I of Ethiopia for financially sponsoring this research.</p><sec id="FPar1"><title>Funding</title><p>Graduate Program of Addis Ababa University and KNCV TB Care I-Ethiopia.</p></sec><sec id="FPar2"><title>Availability of data and materials</title><p>Due to confidentiality issues, the raw data will not be shared.</p></sec><sec id="FPar3"><title>Authors’ contributions</title><p>MS designed the study, supervised the data collection, did the analysis and drafted the manuscript; TGF involved in the design and conduct of the study including approval of the manuscript; GG and DA substantially contributed in data analysis and all authors read and approved the final manuscript.</p></sec><sec id="FPar4"><title>Competing interests</title><p>All authors declared that there is no competing interest.</p></sec><sec id="FPar5"><title>Consent for publication</title><p>Not applicable.</p></sec><sec id="FPar6"><title>Ethics approval and consent to participate</title><p>Ethical approval was obtained from the Research and Ethics Review Committees of the School of Pharmacy, Addis Ababa University, ALERT/AHRI and Addis Ababa Regional Health Bureau. 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