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. 2018 Mar 16;5(4):ofy059. doi: 10.1093/ofid/ofy059

Table 1.

Overview of the Main Studies Reporting on the Prevalence of Tuberculosis and Association With VL Treatment Outcomes in Leishmania donovani-Endemic Countries (1990–2017)

Ref Country, Setting (Healthcare Level), Study Period,
Study Design
Study Population Characteristics and Main VL Treatment TB Diagnosis (Method) Prevalence, Type, and Timing of TBa Early Treatment Outcomes (Death, Treatment Failure) Late Treatment Outcomes: Relapse or Relapse-Free Survival Comments
Ethiopia
[21, 22] NW Ethiopia University hospital and MSF supported health center (2011–2015).
Single-arm pentamidine secondary prophylaxis trial
74 HIV-infected adults, at high risk of VL relapse;
AmBisome 30 mg/kg (±MF); SSG (±PM)
No information 6 of 74 (8.2%) no details on type and timing Relapse: univariate association during and after PM: OR, 1.9 (95% CI, 0.6–6.6); Not retained in multivariate analysis Also no significant association with relapse-free survival
[23] NW Ethiopia, MSF supported health center (2/2008–2/2013)
Retrospective cohort study
146 VL-HIV-coinfected adults
AmBisome 30 mg/kg (±MF)
WHO guidelines 33 of 145 (22%)
no details
Relapse: OR, 1.0 (95% CI, 0.5–2.0)
[24] NW Ethiopia, MSF supported health center and district hospital (1/2007–1/2009)
Retrospective cohort study
195 VL-HIV-coinfected patients
AmBisome 30 mg/kg
No information 58 of 195
(29.7%)
no details
Parasitological failure: no association in multivariate analysis OR, 0.7 (95% CI, 0.2–2.2) In HIV neg: 7.4%
(but 80 of 195 included)
[25] NW Ethiopia, MSF supported district hospital (2003–2006)
Retrospective cohort study
Patients not on ART: 161
Patients on ART: 195
First-line treatment: SSG
No information No ART:
No TB: 64%
TB before VL: 25%
After VL: 8%
Before and after: 2.5%
On ART:
No TB: 41%
TB before VL: 40%
After VL: 16%
Before and after: 2.6%
Death: TB at any time (crude association)
Pts not on ART: OR, 2.1 (95% CI, 0.5–8.7)
Pts on ART: OR, 1.1 (95% CI, 0.5–2.4)
Relapse: crude OR
No ART:
TB before VL: 1.3 (95% CI, 0.6–2.9)
TB after VL: 0.6 (95% CI, 0.1–2.4)
Before and after: 6.3 (95% CI, 1.4–28.0)
On ART
TB before VL: 1.3 (95% CI, 0.6–2.5)
TB after 1.2 (95% CI, 0.5–2.9)
Before and after: 3.1 (95% CI, 0.9–10.5)
Two cases of TB IRIS
Adjusted associations not reported
[16] NW Ethiopia University hospital and district hospital (2006–2008)
Retrospective cohort study
Adult VL-HIV-infected patients, x% male
SSG or AmBisome 30 mg/kg
No information 25 of 92 (27%)
no details
Death or failure: adjusted OR for TB, 4.5 (95% CI, 1.5–13.9) TB prevalence 6% in HIV-negative patients
India
[13] MSF supported district hospital, Bihar, India (2007–2012)
Retrospective cohort study
159 VL-HIV-coinfected patients, 83% male
AmBisome 20–25 mg/kg
No information 9 of 159 (5.7%) no details Mortality: adjusted OR, 3.9 (95% CI, 1.6–9.5) Relapse: crude OR: 2.0 (95% CI, 0.5–8.5)
Not included in multivariate analysis
[14] MSF supported district hospital, Bihar, India (2007–2010)
Retrospective cohort study
55 VL-HIV-coinfected patients AmBisome 20–25 mg/kg, 83% male No information 9 of 55 (16%)
no details
Death or treatment failure: significant association in univariate but not in multivariate analysis Relapse: no significant association in univariate analysis Death: significant association in univariate analysis (multivariate not done given low number)
[15] MSF supported district hospital, Bihar, India (2012–2014)
Retrospective cohort study
102 VL-HIV-coinfected patients; AmBisome 30 mg/kg + MF 14 days, 75% male No information 9 of 102 (8.8%)
no details
Death: adjusted OR, 5.3 (95% CI, 1.6–17.8) Relapse: borderline significant: crude OR, 9.5 (95% CI, 0.9–97.9) Relapse or death: adjusted OR, 7.5 (95% CI, 2.5–22.1)

Abbreviations: ART, antiretroviral therapy; CI, confidence interval; HIV, human immunodeficiency virus; IRIS, immune reconstitution inflammatory syndrome; MF, miltefosine; MSF, Médecins sans Frontières; NW, North-West; PM, paromomycin; Pts, patients; OR, odds ratio; Ref, reference; SSG, sodium stibogluconate; TB, tuberculosis; VL, visceral leishmaniasis; WHO, World Health Organization.

aTiming relative to VL diagnosis: whether the TB diagnosis was before, at the time of, or after the VL diagnosis (eg, during VL treatment).