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Establishment of an information system to support the implementation of a routine neonatal screening strategy for HIV and HBV and to monitor mother-child pairs throughout the continuum of care in Abidjan, Côte d’Ivoire

Software to improve the monitoring of mother-child pairs infected with HIV or HBV: in the delivery room, HIV screening is offered to all women in labor with unknown status; HBV screening is routinely offered, and vaccinated children at Day 0. …

Project Details

Principal Investigator

Dr. Clarisse Bossé (2015–2017); Dr. Maïka Bangali (2017–2019)

Sponsor

EXPETISE France—5% Initiative

Objectives

Main Objectives
Develop, implement, and evaluate a strategy for HIV and HBV screening at birth for mothers and their children, and establish an information system (IS) that tracks exposed mother-child pairs throughout the continuum of care to improve
Secondary Objectives
  • Secondary Objective 1: Develop and implement an information system that will link mothers and children and track them throughout the continuum of care
  • Secondary Objective 2: Identify children exposed to HIV at birth, promote early screening at 6 weeks, and provide HIV-infected mothers with a second opportunity to enter care;
  • Secondary Objective 3: Identify mothers infected with HBV, assess their eligibility for anti-HBV treatment, refer them to appropriate care, and offer the vaccine on Day 0 to exposed children
  • Secondary Objective 4: Evaluate the clinical and economic impact, as well as the cost-effectiveness, of these interventions in Abidjan.
     

Description & Context

Software to improve the monitoring of mother-child pairs infected with HIV or HBV: in the delivery room, HIV screening is offered to all women in labor with unknown status; HBV screening is routinely offered, and vaccinated children at Day 0. Maternal HBV screening and Day 0 vaccination against hepatitis B in the delivery room are well accepted and feasible.

Study Criteria

Inclusion
  • Inclusion criterion 1: being a woman in labor

  • Inclusion criterion 2: Give birth at one of the study facilities during the study period

Exclusion
  • Exclusion criterion 1: having given birth outside the study sites

  • Exclusion criterion 2: having given birth outside the study period

  • Exclusion criterion 3: not having given consent

 

Research Team

The research team has not yet been filled in for this project.

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Keywords

CLINICAL RESEARCH OUR PROJECTS COHORTE
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