Use of Pentamidine As Secondary Prophylaxis to Prevent Visceral Leishmaniasis Relapse in HIV Infected Patients, the First Twelve Months of a Prospective Cohort Study

PLoS Negl Trop Dis. 2015 Oct 2;9(10):e0004087. doi: 10.1371/journal.pntd.0004087. eCollection 2015.

Abstract

Background: Visceral leishmaniasis (VL) has become an important opportunistic infection in persons with HIV-infection in VL-endemic areas. The co-infection leads to profound immunosuppression and high rate of annual VL recurrence. This study assessed the effectiveness, safety and feasibility of monthly pentamidine infusions to prevent recurrence of VL in HIV co-infected patients.

Methods: A single-arm, open-label trial was conducted at two leishmaniasis treatment centers in northwest Ethiopia. HIV-infected patients with a VL episode were included after parasitological cure. Monthly infusions of 4 mg/kg pentamidine-isethionate diluted in normal-saline were started for 12 months. All received antiretroviral therapy (ART). Time-to-relapse or death was the primary end point.

Results: Seventy-four patients were included. The probability of relapse-free survival at 6 months and at 12 months was 79% and 71% respectively. Renal failure, a possible drug-related serious adverse event, occurred in two patients with severe pneumonia. Forty-one patients completed the regimen taking at least 11 of the 12 doses. Main reasons to discontinue were: 15 relapsed, five died and seven became lost to follow-up. More patients failed among those with a CD4+cell count ≤ 50 cells/μl, 5/7 (71.4%) than those with counts above 200 cells/μl, 2/12 (16.7%), (p = 0.005).

Conclusion: Pentamidine secondary prophylaxis led to a 29% failure rate within one year, much lower than reported in historical controls (50%-100%). Patients with low CD4+cell counts are at increased risk of relapse despite effective initial VL treatment, ART and secondary prophylaxis. VL should be detected and treated early enough in patients with HIV infection before profound immune deficiency installs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIDS-Related Opportunistic Infections / prevention & control*
  • Adult
  • Antiprotozoal Agents / therapeutic use*
  • Cohort Studies
  • Female
  • Humans
  • Leishmaniasis, Visceral / prevention & control*
  • Male
  • Pentamidine / adverse effects
  • Pentamidine / therapeutic use*
  • Prospective Studies
  • Recurrence

Substances

  • Antiprotozoal Agents
  • Pentamidine

Grants and funding

This work was supported by the European Union Seventh Framework Programme (FP7/2007‐2013) under grant agreement n° 305178 via AfriCoLeish project, and the Drugs for Neglected Diseases initiative. ED has received a PhD scholarship granted from the Belgian Directorate General for Development Cooperation under the ITM-DGDC framework agreement FA-III and from the European Union Seventh Framework Programme through AfriCoLeish Project. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.