Evidence map›Paper›PMID 37474229›Full record

Trial reportThe Lancet. Global health2023

Incorporating the HIV Infant Tracking System into standard-of-care early infant diagnosis of HIV services in Kenya: a cost-effectiveness analysis of the HITSystem randomised trial.

Sarah Finocchario-Kessler, Kathy Goggin, Catherine Wexler, May Maloba, Brad Gautney, Samoel Khamadi, Raphael Lwembe, Shadrack Babu, Michael Sweat

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Lancet. Global health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Sarah Finocchario-KesslerDepartment of Family Medicine and Community Health, University of Kansas Medical Center, Kansas City, KS, USA. Electronic address: skessler2@kumc.edu.
Kathy GogginHealth Services and Outcomes Research, Department of Pediatrics, Children's Mercy Hospital, Kansas City, MO, USA.
Catherine WexlerDepartment of Family Medicine and Community Health, University of Kansas Medical Center, Kansas City, KS, USA.
May MalobaGlobal Health Innovations Kenya, Nairobi, Kenya.
Brad GautneyGlobal Health Innovations, Dallas, TX, USA.
Samoel KhamadiCentre for Virus Research, Kenya Medical Research Institute, Nairobi, Kenya.
Raphael LwembeCentre for Virus Research, Kenya Medical Research Institute, Nairobi, Kenya.
Shadrack BabuGlobal Health Innovations Kenya, Nairobi, Kenya.
Michael SweatDivision of Global and Community Health, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Kenya Medical Research Institute · KEUniversity of Kansas Medical Center · USChildren's Mercy Hospital · USHealth Innovations (United States) · USMedical University of South Carolina · US

Funding

Evaluating the HITSystem to Improve PMTCT Retention and Maternal Viral Suppression in KenyaR01MH121245 · NIMH · UNIVERSITY OF KANSAS MEDICAL CENTER · PI KESSLER, SARAH FINOCCHARIO · 2020 to 2024
$3.5M
Piloting at-birth point of care HIV testing strategies in KenyaR01HD076673 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI KESSLER, SARAH FINOCCHARIO · 2013 to 2017
$3.4M
NICHD NIH HHS R01 HD076673NIMH NIH HHS R01 MH121245
6 · The paper itself

Abstract

backgroundThe HITSystem efficacy trial showed significant improvements in early infant diagnosis retention, return and notification of infant test results, and earlier antiretroviral therapy (ART) initiation compared with standard-of-care early infant diagnosis services in Kenya. This study aimed to analyse data from the HITSystem trial to assess the cost-effectiveness of the intervention in Kenya.

methodsIn this analysis, we extrapolated results from the HITSystem cluster randomised controlled trial to model early infant diagnosis outcomes and cost-effectiveness if the HITSystem was scaled up nationally in Kenya, compared with standard-of-care outcomes. We used a micro-costing method to collect cost data, which were analysed from a health-system perspective, reflecting the investment required to add HITSystem to existing early infant diagnosis services and infrastructure. The base model used to calculate cost-effectiveness was deterministic and calculated the progression of infants through early infant diagnosis. Differences in progression across study arms were used to establish efficacy outcomes. The number of life-years gained per infant successfully initiating ART were based on the Cost Effectiveness of Preventing AIDS Complications model in east Africa. HITSystem cost data were integrated into the model, and the incremental cost-effectiveness ratio was calculated in terms of cost per life-year gained. Sensitivity analyses were done using the deterministic model with triangular stochastic probability functions for key model parameters added. The number of life-years gained was discounted at 3% and costs were adjusted to 2021 values.

findingsThe cost per life-year gained from the HITSystem was US$82·72. Total cost for national HITSystem coverage in Kenya was estimated to be around $2·6 million; covering 82 230 infants exposed to HIV at a cost of $31·38 per infant and a yield of 1133 infants receiving timely ART, which would result in 31 189 life-years gained. With sensitivity analyses, the cost per life-year gained varied from $40·13 to $215·05. 90% of model values across iterations ranged between $55·58 (lower 5% threshold) and $132·38 (upper 95% threshold).

interpretationThe HITSystem would be very cost-effective in Kenya and can optimise the return on the existing investment in the national early infant diagnosis programme.

fundingThe US National Institute of Child Health and Human Development.

Indexed as

Cost-Effectiveness AnalysisHIV InfectionsAfrica, EasternChildCost-Benefit AnalysisEarly DiagnosisHumansInfantKenya

Identifiers

PMID37474229
PMCPMC10482001
OpenAlexW4384922267

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.