Literature DB >> 28049455

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.

Mahlet Semu1, Teferi Gedif Fenta2, Girmay Medhin3, Dawit Assefa4.   

Abstract

BACKGROUND: 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.
METHODS: 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.
RESULTS: 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.
CONCLUSIONS: 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.

Entities:  

Keywords:  Ethiopia; IPT; Incidence of active TB; TB/HIV co-infection

Mesh:

Substances:

Year:  2017        PMID: 28049455      PMCID: PMC5209939          DOI: 10.1186/s12879-016-2109-7

Source DB:  PubMed          Journal:  BMC Infect Dis        ISSN: 1471-2334            Impact factor:   3.090


Background

Tuberculosis (TB) and Human Immunodeficiency virus/Acquired Immunodeficiency Syndrome (HIV/AIDS) are major public health threat [1-3]. 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 [2, 4, 5]. HIV infection is also the strongest risk factor for TB disease [3]. 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 [5]. 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 [6]. 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 [7]. 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 [8]. According to WHO [2], 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% [9]. 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[10]. 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.

Methods

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.

Results

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 1).
Table 1

Socio-demographic characteristics of patients at enrollment for chronic HIV care in public health facilities of Addis Ababa, during 2007-June 2012

Socio-demographic profile at enrollment for HIV care (N = 2524)IPT Exposed N (%)IPT Non-exposed N (%)Total N (%)Chi-square P value
Sex
 Male473(37.4)469(37.2)942(37.3)0.918
 Female791(62.6)791(62.8)1582(62.7)
Age in years (mean = 34.9, SD = 9.1)
 <30421(33.3)557(44.2)978(38.7)0.150
 30–39408(32.3)412(32.7)820(32.5)
 40–49283(22.4)247(19.6)530(21)
 >50152(12)44(3.5)196(7.8)
Marital status
 Single318(25.2)288(22.9)606(24)0.000
 Married584(46.2)551(43.7)1135(45)
 Widowed189(15)195(15.5)384(15.2)
 Separated157(12.4)165(13.1)322(12.8)
 Divorced16(1.3)61(4.8)77(3.1)
Level of Education
 No formal education248(19.6)276(21.9)524(20.8)0.004
 Primary completed507(40.1)447(35.5)954(37.8)
 Secondary completed473(37.4)473(37.5)946(37.5)
 Tertiary completed36(2.8)64(5.1)100(4)
Religion
 Orthodox979(77.5)1023(81.2)2002(79.3)0.197
 Muslim98(7.8)177(14)275(10.9)
 Protestant132(10.4)54(4.3)236(9.4)
 Othersa 5(0.4)6(0.5)11(0.4)
Employment status
 Non-employed650(51.4)483(38.3)1133(44.9)0.000
 Self-employed218(17.2)247(19.6)465(18.4)
 Government employed205(16.2)248(19.7)453(17.95)
 Private183(14.5)270(21.4)453(17.95)
 Student8(0.63)12(0.95)20(0.8)
Residence place
 Addis Ababa1230(97.3)1252(99.4)2482(98.3)0.322
 Out of Addis Ababa34(2.7)8(0.6)42(1.7)
Average no. of personnel per family3.153.453.30.092
Average no. of rooms per family1.351.651.50.593

aCatholic and Joba

Socio-demographic characteristics of patients at enrollment for chronic HIV care in public health facilities of Addis Ababa, during 2007-June 2012 aCatholic and Joba 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 2. 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 2

Baseline clinical information of HIV positive patients in public health facilities of Addis Ababa, during 2007-June 2012

Baseline Clinical status (N = 2524)IPT Exposed N (%)IPT Non-exposed N (%)Total N (%)Chi-square P value
Initial WHO stage of HIV/AIDS
 Stage 1357(28.2)215(17.1)572(22.7)0.000
 Stage 2487(38.5)346(27.5)833(33)
 Stage 3392(31)580(46)972(38.5)
 Stage 428(2.3)119(9.4)147(5.8)
Baseline CD4cells count/μl(mean = 230, SD = 176.9)
 ≤200570(45.1)807(64)1377(54.6)0.000
 >200694(54.9)453(36)1147(45.4)
Initial body weight in Kg (mean = 53.8, SD = 9.7)
 <50304(24.1)554(43.8)858(34)0.009
 50–59628(49.7)418(33.1)1046(41.4)
 60–69208(16.5)214(17)422(16.7)
 >69124(9.8)74(5.9)198(7.8)
TB screeneda
 Positive040(3.2)40(1.6)
 Negative1264(100)1220(96.8)2484(98.4)
 On CPT
 Yes1259(99.6)1205(95.6)2464(97.6)0.000
 No5(0.4)55(4.4)60(2.4)
OIs diagnosed
 None1082(85.6)907(71.9)1989(78.8)0.000
 Bacterial infections11(0.87)164(13)175(6.9)
 Viral infections25(0.08)88(6.9)113(4.5)
 Fungal infections38(3)129(10.2)167(6.6)
 Viral & bacterial infections20(1.6)13(1.03)33(1.3)
 Bacterial & fungal infections11(0.87)8(0.63)19(0.8)
 Fungal & viral infections8(0.6)12(0.95)20(0.8)

aA 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

Baseline clinical information of HIV positive patients in public health facilities of Addis Ababa, during 2007-June 2012 aA 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 As shown in Table 3, 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 3

Clinical information of patients who were unheard follow upinpublic health facilities of Addis Ababa, during 2007-June 2012

Clinical information when ART initiated (N = 2046)IPT exposed N (%)IPT Non-exposed N (%) N (%)Chi-square P value
WHO stage of HIV/AIDS
 Stage 1151(16.02)138(12.5)289(14.1)0.000
 Stage 2367(39)294(26.6)661(32.3)
 Stage 3394 (41.8)551(49.9)945(46.2)
 Stage 430 (3.18)121(11.0)151(7.4)
CD4cells count/μl(mean = 151.2, SD = 84.9)
 ≤200537 (37.9)1020(92.4)1557(76.1)0.000
 >200263 (27.9)226(20.5)489(23.9)
Weight in Kg (mean = 53.2, SD = 9.5)
 <50241(25.6)506(45.8)747(36.5)0.011
 50–59479(44.2)366(33.1)845(41.3)
 60–69164 (17.4)164(14.9)328(16.0)
 >6958 (6.2)68(6.2)126(6.2)
TB screened
 Yes942(100)1100(99.6)2042(99.8)0.64
 No04(0.4)4(0.2)
CPT adherence
 Good791(84)1096(99.3)2032(99.6)0.046
 Fair3(.32)6(0.5)9(0.3)
 Poor3(.32)2(0.2)5(0.2)
ART adherence
 Good937(99.5)1100(99.6)2037(99.6)0.124
 Fair5(0.53)2(0.2)7(0.3)
 Poor02(0.2)2(0.1)
OIs after ART initiated
 None937(99.5)1052(95.3)1989(97.21)0.000
 Fungal3(.32)20(1.8)23(1.12)
 Viral012(1.0)12(0.5)
 Bacterial012(1.0)14(0.7)
 Bacterial & fungal04(0.4)4(0.2)
 Othersa 04(0.4)4(0.2)

aProtozoal, viral & bacterial & fungal & viral infections

Clinical information of patients who were unheard follow upinpublic health facilities of Addis Ababa, during 2007-June 2012 aProtozoal, viral & bacterial & fungal & viral infections 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 4).
Table 4

Profile of IPT exposed patients inpublic health facilities of Addis Ababa, during 2007-June 2012

Profile (N = 1264) N (%)Chi-square P-value
 Male473(37.4%)
 Female791(62.6%)
TB screened & tested negative1264(100%)
Currently on HAART942(74.5%)
Pre-ART322(25.5%)
HAART initiated before IPT578(61.3%)
HAART initiated after IPT364(38.7%)
IPT completed975(77.1%)
IPT discontinued289(22.9%)
On HAART + IPT completed738(78.3%)0.094
Pre-ART + IPT completed237(73.6%)
On HAART + IPT in-completed204(21.7%)0.08
Pre-ART + IPT in-completed85(26.4%)
Male IPT completed359(75.9%)0.459
Female IPT completed616(77.8%)
Took B6 together with INH581(46%)
No IPT side effects1254(99.2%)
Profile of IPT exposed patients inpublic health facilities of Addis Ababa, during 2007-June 2012 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 CD4 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 5, Fig. 1).
Table 5

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

Patient profileEvent/P/YIR/100P-YCrude IRR (95% CI)Adjusted IRR(95% CI)
Over all277/41066.7
IPT completed7/33.30.210.03(0.01–0.06)0.04(0.05–0.07)
IPT in-completed8/7.80.860.84(0.36–1.33)0.89(0.49–1.76)
IPT non-exposed262/36.497.1811
Sex
 Male138/2822.14.891.80(1.42–2.28)1.59(1.20–2.12)
 Female139/5129.22.7111
Age group in year
 <30103/3038.33.3911
 30–3987/2628.43.310.98(0.73–1.29)0.82(0.61–1.11)
 40–4961/1644.23.711.09(0.79–1.49)1.04(0.74–1.47)
 >4926/637.34.081.201(0.77–1.82)1.55(0.95–2.44)
Residence area
 Living out of Addis Ababa4/135.12.960.85(0.26–1.99)0.29(0.09–0.73)
 Living in Addis Ababa273/78003.5011
Religion
 Orthodox231/6243.23.700.63(0.20–3.82)0.29(0.08–1.86)
 Muslim19/8922.130.36(0.11–2.28)0.17(0.04–1.13)
 Protestant25/778.83.210.55(0.16–3.40)0.32(0.09–2.12)
 Others*11/187.75.8611
Marital status
 Married127/3547.53.580.82(0.46–1.68)1.22(0.66–2.51)
 Single72/1889.83.810.88(0.48–1.81)1.18(0.63–2.48)
 Widowed33/12842.570.59(0.30–1.27)0.81(0.40–1.76)
 Divorced35/997.23.510.81(0.45–1.72)1.05(0.53–2.27)
 Separated10/229.94.3511
Employment
 Self employed87/3782.62.300.03(0.01–0.19)0.02(0.01–0.12)
 Private Employed58/1418.14.090.06(0.02–0.35)0.03(0.01–0.16)
 Government employed62/1324.84.680.07(0.02–0.40)0.03(0.01–0.19)
 Student3/66.54.510.06(0.01–0.48)0.01(0.002–0.101)
 Non- employed65/1354.24.8011
Educational level
 None educated42/1707.32.460.65(0.35–1.33)1.25(0.62–2.70)
 Primary Completed106/3028.63.500.93(0.52–1.83)1.69(0.89–3.49)
 Secondary Completed118/2920.84.041.07(0.60–2.10)1.76(0.97–3.55)
 Tertiary completed11/2913.7811
House Hold size/room no.0.99(0.89–1.09)0.98(0.88–1.07)
Baseline WHO stage of HIV/AIDS
 Stage 1 & 245/4545.50.990.14(0.10–0.19)0.23(0.16–0.31)
 Stage 3 & 4232/3381.96.861
Baseline CD4 cells/μl
 ≤200211/4169.95.062.89(2.21–3.85)1.36(1.02–1.84)
 >20066/3771.41.75
Baseline weight in Kg
 ≤49113/2646.44.271.88(1.12–3.43)1.63(0.93–3.05)
 50–59108/3343.73.231.42(0.85–2.59)1.19(0.69–2.22)
 60–6942/1333.33.151.39(0.78–2.64)1.06(0.59–2.03)
 >6914/616.72.2711
Baseline OIs
 Yes194/6278.33.090.62(0.48–0.80)1.24(0.95–1.63)
 No83/16605.0011
CPT adherence
 Good271/77653.490.99(0.48–2.51)0.92(0.44–2.37)
 Fair, Poor & no CPT2/56.83.5211

*others include: catholic, johoba and non belivers

Fig. 1

Incidence rate among IPT completed, in-completed and non- exposed patientsin public health facilities of Addis Ababa, during 2007-June 2012

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 *others include: catholic, johoba and non belivers Incidence rate among IPT completed, in-completed and non- exposed patientsin public health facilities of Addis Ababa, during 2007-June 2012 Similarly, as shown in Table 6 and Fig. 2, 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 6

IR & IRR among patients who took HAART with or without IPT in public health facilities of Addis Ababa, during 2007-June 2012

Therapy (N = 1842)IR/100P-YaIRR(95% CI)
 IPT with HAART0.420.063(0.035–0.104)
 HAART only7.831
IPT initiation time with HAART
 Took IPT with HAART0.20.158(0.039–0.555)
 Took IPT before initiating HAART0.751
Fig. 2

IR among patients who took HAART with IPT in public health facilities of Addis Ababa, during 2007-June 2012

IR & IRR among patients who took HAART with or without IPT in public health facilities of Addis Ababa, during 2007-June 2012 IR among patients who took HAART with IPT in public health facilities of Addis Ababa, during 2007-June 2012 As shown in Table 7, there was significant CD4 and weight changes among IPT-HAART treated patients.
Table 7

Statistical analysis of clinical data among patients who took HAART with IPT in public health facilities of Addis Ababa, during 2007-June 2012

Variables N Mean Rank P- value
Weight after completing IPT – weight at enrollmentNegative Ranks160a 410.64
Positive Ranks701b 435.650.000
Ties114c
Total975
CD4 after completing IPT - CD4 at enrollmentNegative Ranks253d 546.73
Positive Ranks702e 453.230.000
Ties21f
Total976

aWeight when completing IPT < weight when starting IPT

bWeight when completing IPT > weight when starting IPT

cWeight when completing IPT = weight when starting IPT

dCD4 when completing IPT < CD4 when starting IPT

eCD4 when completing IPT > CD4 when starting IPT

fCD4 when completing IPT = CD4 when starting IPT

Statistical analysis of clinical data among patients who took HAART with IPT in public health facilities of Addis Ababa, during 2007-June 2012 aWeight when completing IPT < weight when starting IPT bWeight when completing IPT > weight when starting IPT cWeight when completing IPT = weight when starting IPT dCD4 when completing IPT < CD4 when starting IPT eCD4 when completing IPT > CD4 when starting IPT fCD4 when completing IPT = CD4 when starting IPT 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 19thmonth; while in non-exposed patients TB occurred within a month time of enrollment (Table 8).
Table 8

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

VariablesNo of patients active TB diagnosedMinimum month TB occurredMaximum month TB occurredMean month TB occurredStandard DeviationMedian
Month TB occurred among IPT completed patients762816.78.419
Month TB occurred among patients who discontinued IPT80359.614.80
Month TB occurred among IPT non-exposed2620658.113.31
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 As shown in Table 9, 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 9

TB incidence in month interval among IPT completed, in-completed & non-exposed patients in public health facilities of Addis Ababa, during 2007-June 2012

Follow up monthIPT exposure/completion statusIR/100 P-M (95% CI)Unadjusted IRR (95% CI)Adjusted IRR (95% CI)
<6Completed000
In-complete142.8(17.64–268.07)1.82(0.65–3.97)2.125(0.712–5.103)
Non-exposed78.59(66.9–90.3)11
6–12Completed12(1.58–25.58)0.30(0.06–0.79)0.03(0.013–1.95)
In-completed38.71(7.74–69.68)0.98(0.39–2.02)1.05(0.32–2.89)
Non-exposed39.43(34.05–44.82)11
12–24Completed6.74(1.35–12.14)0.29(0.11–0.59)0.03(0.01–0.74)
In-completed38.71(7.74–69.68)1.65(0.65–3.38)1.61(0.51–4.29)
Non-exposed23.51(20.48–26.55)11
24–36Completed5.98(1.55–10.42)0.34(0.14–0.66)0.04(0.02–1.74)
In-completed9.94(3.05–16.82)0.56(0.25–1.05)1.09(0.49–2.54)
Non-exposed17.87(15.63–20.11)11
37–48Completed5.98(1.55–10.42)0.44(0.186–0.854)0.74(0.301–1.56)
In-completed9.94(3.05–16.82)0.73(0.33–1.37)0.72(0.314–1.44)
Non-exposed13.72(12.04–19.5611
>48Completed5.98(1.55–10.42)0.50(0.22–0.99)0.88(0.36–1.84)
In-completed9.94(3.05–16.82)0.84(0.38–1.58)0.89(0.39–1.76)
Non-exposed11.88(10.44–13.32)11
TB incidence in month interval among IPT completed, in-completed & non-exposed patients in public health facilities of Addis Ababa, during 2007-June 2012

Discussion

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 [11-13]. 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 [7, 14–16]. 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. Among patients who completed IPT, though TB had occurred after 6 months, almost 50% of them developed TB at 19thmonth; 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 [17]. 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 [10]. It is, however, better than reports from South East Asian and other Sub-Saharan African countries [13, 17, 18]. 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) & CD4 cell count (less than 200cells/μl). Similarly, South African and Namibian studies indicated the influence of clinical factors on the incidence of Tb among HIV patients [13, 16]. Getahun et al. [19] 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. [20]. 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 CD4cell 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.

Conclusions

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, CD4 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.
  9 in total

1.  Tuberculosis and HIV coinfection: current state of knowledge and research priorities.

Authors:  Gerald Friedland; Gavin J Churchyard; Edward Nardell
Journal:  J Infect Dis       Date:  2007-08-15       Impact factor: 5.226

2.  Tuberculosis in HIV programmes in lower-income countries: practices and risk factors.

Authors:  L Fenner; M Forster; A Boulle; S Phiri; P Braitstein; C Lewden; M Schechter; N Kumarasamy; M Pascoe; E Sprinz; D R Bangsberg; P S Sow; D Dickinson; M P Fox; J McIntyre; M Khongphatthanayothin; F Dabis; M W G Brinkhof; R Wood; M Egger
Journal:  Int J Tuberc Lung Dis       Date:  2011-05       Impact factor: 2.373

Review 3.  HIV infection-associated tuberculosis: the epidemiology and the response.

Authors:  Haileyesus Getahun; Christian Gunneberg; Reuben Granich; Paul Nunn
Journal:  Clin Infect Dis       Date:  2010-05-15       Impact factor: 9.079

4.  Isoniazid preventive therapy and 4-year incidence of pulmonary tuberculosis among HIV-infected Thai patients.

Authors:  T Khawcharoenporn; A Apisarnthanarak; W Manosuthi; S Sungkanuparph; L M Mundy
Journal:  Int J Tuberc Lung Dis       Date:  2012-01-05       Impact factor: 2.373

5.  Effect of routine isoniazid preventive therapy on tuberculosis incidence among HIV-infected men in South Africa: a novel randomized incremental recruitment study.

Authors:  Alison D Grant; Salome Charalambous; Katherine L Fielding; John H Day; Elizabeth L Corbett; Richard E Chaisson; Kevin M De Cock; Richard J Hayes; Gavin J Churchyard
Journal:  JAMA       Date:  2005-06-08       Impact factor: 56.272

Review 6.  Treatment of latent tuberculosis infection in HIV infected persons.

Authors:  S Woldehanna; J Volmink
Journal:  Cochrane Database Syst Rev       Date:  2004

Review 7.  Early mortality among adults accessing antiretroviral treatment programmes in sub-Saharan Africa.

Authors:  Stephen D Lawn; Anthony D Harries; Xavier Anglaret; Landon Myer; Robin Wood
Journal:  AIDS       Date:  2008-10-01       Impact factor: 4.177

8.  Effectiveness and safety of isoniazid chemoprophylaxis for HIV-1 infected patients from Rio de Janeiro.

Authors:  Claudia Teresa Vieira de Souza; Yara Hahr Marques Hökerberg; Sandro Javier Bedoya Pacheco; Valéria Cavalcanti Rolla; Sonia Regina Lambert Passos
Journal:  Mem Inst Oswaldo Cruz       Date:  2009-05       Impact factor: 2.743

9.  Isoniazid preventive therapy, HAART and tuberculosis risk in HIV-infected adults in South Africa: a prospective cohort.

Authors:  Jonathan E Golub; Paul Pronyk; Lerato Mohapi; Nkeko Thsabangu; Mosa Moshabela; Helen Struthers; Glenda E Gray; James A McIntyre; Richard E Chaisson; Neil A Martinson
Journal:  AIDS       Date:  2009-03-13       Impact factor: 4.177

  9 in total
  20 in total

1.  Incidence of tuberculosis among PLHIV on antiretroviral therapy who initiated isoniazid preventive therapy: A multi-center retrospective cohort study.

Authors:  Andrew Kazibwe; Bonniface Oryokot; Levicatus Mugenyi; David Kagimu; Abraham Ignatius Oluka; Darlius Kato; Simple Ouma; Edmund Tayebwakushaba; Charles Odoi; Kizito Kakumba; Ronald Opito; Ceasar Godfrey Mafabi; Michael Ochwo; Robert Nkabala; Wilber Tusiimire; Agnes Kateeba Tusiime; Sarah Barbara Alinga; Yunus Miya; Michael Bernard Etukoit; Irene Andia Biraro; Bruce Kirenga
Journal:  PLoS One       Date:  2022-05-16       Impact factor: 3.752

2.  "Universal test and treat" program reduced TB incidence by 75% among a cohort of adults taking antiretroviral therapy (ART) in Gurage zone, South Ethiopia.

Authors:  Tadele Girum; Fedila Yasin; Samuel Dessu; Bereket Zeleke; Mulugeta Geremew
Journal:  Trop Dis Travel Med Vaccines       Date:  2020-07-31

3.  Determinants of alcohol use among people living with HIV initiating isoniazid preventive therapy in Ethiopia.

Authors:  Trena I Mukherjee; Yael Hirsch-Moverman; Suzue Saito; Tsigereda Gadisa; Zenebe Melaku; Andrea A Howard
Journal:  Drug Alcohol Depend       Date:  2019-08-30       Impact factor: 4.492

4.  Utilization of isoniazid prophylaxis therapy and its associated factors among HIV positive clients taking antiretroviral therapy at Fre Semaetat primary hospital, Hawzien districts, Tigrai, Northern Ethiopia.

Authors:  Haftom Legese; Hagos Degefa; Aderajew Gebrewahd; Haftay Gebremedhin
Journal:  Trop Dis Travel Med Vaccines       Date:  2020-06-17

5.  Tuberculosis and its association with CD4+ T cell count among adult HIV positive patients in Ethiopian settings: a systematic review and meta-analysis.

Authors:  Demeke Geremew; Mulugeta Melku; Aklilu Endalamaw; Berhanu Woldu; Alebachew Fasil; Markos Negash; Habtamu Wondifraw Baynes; Habtamu Geremew; Takele Teklu; Tekalign Deressa; Belay Tessema; Ulrich Sack
Journal:  BMC Infect Dis       Date:  2020-05-07       Impact factor: 3.090

6.  The protective effect of isoniazid preventive therapy on tuberculosis incidence among HIV positive patients receiving ART in Ethiopian settings: a meta-analysis.

Authors:  Demeke Geremew; Aklilu Endalamaw; Markos Negash; Setegn Eshetie; Belay Tessema
Journal:  BMC Infect Dis       Date:  2019-05-10       Impact factor: 3.090

7.  Assessing the Impact of Isoniazid Preventive Therapy (IPT) on Tuberculosis Incidence and Predictors of Tuberculosis among Adult Patients Enrolled on ART in Nekemte Town, Western Ethiopia: A Retrospective Cohort Study.

Authors:  Gemechu Tiruneh; Alemayehu Getahun; Emiru Adeba
Journal:  Interdiscip Perspect Infect Dis       Date:  2019-05-02

8.  Effect of Isoniazid Prophylaxis Therapy on the Prevention of Tuberculosis Incidence and Associated Factors Among HIV Infected Individuals in Northwest Ethiopia: Retrospective Cohort Study.

Authors:  Mulat Addis Beshaw; Shitaye Alemu Balcha; Ayenew Molla Lakew
Journal:  HIV AIDS (Auckl)       Date:  2021-06-08

9.  Factors associated with prognostic or treatment outcomes in HIV/AIDS patients with and without hypertension in Eswatini.

Authors:  Sabelo Bonginkosi Dlamini; Hans-Uwe Dahms; Ming-Tsang Wu
Journal:  Sci Rep       Date:  2021-06-21       Impact factor: 4.379

10.  Prevalence of Smear-Positive Tuberculosis among Patients Who Visited Saint Paul's Specialized Hospital in Addis Ababa, Ethiopia.

Authors:  Dinna Abera Nugussie; Getachew Ali Mohammed; Anteneh Tesfaye Tefera
Journal:  Biomed Res Int       Date:  2017-08-21       Impact factor: 3.411

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.