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Outcomes among patients with HIV- associated Tuberculosis in Guangxi, People’s Republic of China Zhang Yao, Yu Lan, Ma Ye, Zhao Yan, Sun Kai and Zhang.

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Presentation on theme: "Outcomes among patients with HIV- associated Tuberculosis in Guangxi, People’s Republic of China Zhang Yao, Yu Lan, Ma Ye, Zhao Yan, Sun Kai and Zhang."— Presentation transcript:

1 Outcomes among patients with HIV- associated Tuberculosis in Guangxi, People’s Republic of China Zhang Yao, Yu Lan, Ma Ye, Zhao Yan, Sun Kai and Zhang Fujie Division of Treatment and Care National Center for AIDS/STD Chinese Center of Disease Control and Prevention

2 Background  TB is the most common co-infection in HIV infected population.  China is a high TB burden country with a growing HIV epidemic.  HIV-associated TB – a particular problem due to its high mortality, diagnostic challenges, and complicated simultaneous treatment of both infections – is therefore a growing concern in China.  Yet outcomes among patients with HIV associated TB in China are not well characterized.

3 Objective  This study seeks to evaluate the magnitude and determinants of survival among HIV infected patients with culture positive tuberculosis seeking care in the public health system in Guangxi province, China.

4 Design & Patients  Retrospective cohort study.  Patients were identified from a cross sectional TB screening project during 2006-2008.  Adult(>18y) HIV+ patients with a positive TB culture from any body fluid were included and followed until 12 month after TB diagnosis, or death, loss to follow-up, or transfer if earlier.

5 Study sites Total population: 10 million HIV prevalence: 0.1% TB prevalence in PLWH: 20%

6 Treatment guidelines  ART starting criteria: changed from CD4<200 to CD4<350 in 2008  ART regimen: AZT(d4T) + 3TC + EFV(NVP)  Timing of ART initiation in ART-Naïve patients with active TB: CD4<200: 2–8 weeks after TB therapy initiation CD4=200-350: after 8 weeks TB induction period CD4>350: after completion of TB therapy  TB regimen: RHZE x 2months then RH x 4months, adjusted according to drug resistance testing

7 Measurements  Primary outcome of interest: all cause mortality within first 12 months of TB diagnosis.  Clinic records were reviewed at 12 month after the TB diagnosis to ascertain vital status, then confirmed with national HIV database.  Socio-demographic and clinical information were extracted from patients’ charts.  Liquid culture(BacT/Alert) was used for diagnosis and TB drug resistance testing for isoniazid, rifampin, ethambutol, streptomycin.

8 Statistical analysis  The Kaplan–Meier method was used to estimate the probability of death after TB diagnosis.  Cox regression was used to determine risk factors associated with mortality.  Logistic regression was used to determine factors associated with receipt of TB therapy and ART.

9 Results-baseline characteristics (n=201) VariableValue Age, years, Median (IQR)37(30-46) Male gender, n (%)163 (81) Transmission Route, n(%) Sex 102 (51) IDU 62 (31) Former plasma donor 3 (2) Unknown 34 (17) History of TB treatment, n(%)13 (7) On ART at TB diagnosis, n(%)69 (34) Baseline CD4, median (IQR)37 (16-101) Extra-pulmonary TB, n(%)111 (55)

10 Sources of culture samples by location, n(%) Sputum 168 (84) Lymph node aspiration 39 (19) Blood 22 (11) Stool 11 (6) Cerebral Spinal Fluid 7 (4) Pleural fluid 7 (4) Note: some patients had positive cultures from more than one sources.

11 Drug resistance pattern of 156 M.tuberculosis strains

12 TB and ARV Treatment Coverage (67%)

13 Results – 1 year clinical outcomes Total=201 Alive: 123 (61%) Dead: 47 (23%) Transferred: 17 (9%) LTFU: 14 (7%) Accumulative Survival =75% (95%CI, 69-81%)

14 Risk Factors Associated with Death * Adjusted for gender, age, mode of transmission, CD4 at study entry, extrapulmonary TB, TB drug resistance and ART status at study entry Risk factors UnivariateMultivariate* PvalueHR(95% CI)P valueHR (95% CI) BMI<180.012.1(1.8-3.9)0.0042.9(1.4-6.1) ART during study period <0.00010.2(0.1-0.4)0.0010.3(0.1-0.6) TB therapy during study period <0.00010.2(0.1-0.3)0.010.3(0.1-0.8) Cotrimoxazole prophylaxis 0.0050.3(0.1-0.7)0.280.5(0.2-1.7)

15 Survival of patients by Treatment status AHR=6; CI [3-13] AHR=7; CI [3-18] AHR=24; CI [9-62] HR=1;ref

16 Factors associated with death or LTFU variables UnivariateMultivariate* P valueHR (95% CI)P valueHR (95% CI) BMI <180.0072.1(1.2-3.5)<0.00013.3(1.7-6.2) ART during study period <0.00010.14 (0.1-0.2)<0.00010.2(0.1-0.3) TB Tx during study period <0.00010.2 (0.1-0.3)0.0190.4(0.2-0.9) Cotrimoxazole prophylaxis <0.00010.3(0.1-0.5)0.270.6(0.3-1.5) * Adjusted for gender, age, mode of transmission, CD4, extrapulmonary TB, TB drug resistance, and ART status on study entry

17 Factors associated Receiving ARV variables UnivariateMultivariate* P valueOR (95% CI)P valueOR (95% CI) Education (above vs. below middle school) 0.0332.0(4.0-1.1)0.0581.9(3.8-1.0) Marital status (married vs. not married) 0.0282.1 (1.1-4.1)0.0282.1(1.1-4.2) Received TB Tx0.00173.6 (1.6-8.1)0.0352.6(1.1-6.4) * Adjusted for gender, age, BMI, mode of transmission, baseline CD4, CXR, and sputum smear

18 Factors associated with TB Treatment variables UnivariateMultivariate* P valueOR (95% CI)P valueOR (95% CI) CXR (typical vs. others) 0.0144.0(1.3-12)0.0588.1(0.93-72) Positive sputum smear 0.0433.4 (1.0-11)0.0534.1(0.98-17) * Adjusted for gender, age, literacy, marital status, mode of transmission, BMI, baseline CD4, EPTB and sputum smear

19 Conclusions and implications  This cohort of HIV+ Chinese adults with culture-positive TB demonstrated high tuberculosis drug resistance rate, high 1 year mortality and lower-than-expected treatment coverage.  These findings implicate that strengthening integrated administration of ART and TB therapies are critically important in this setting.

20 Acknowledgement Sponsors: Clinton Foundation, Global Fund Guangxi Province Health Department: Drs. Liu Wei, Tang Zhirong, Lu Hongyan Liu Zhou CDC: Zheng Yuanjia, MD Naning 4 th Hospital: Huang Shaobiao, MD University of California, San Francisco: Elvin Geng, MD University of North Carolina: Zhu Hao, Ph.D National Institute of Health: Ray Y, Chen, MD University of California, Los anginas : Wen Yi, Ph.D World Health Organization: Fabio Scano Washington University: Maurer Kristin


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