Evidence map›Paper›PMID 38569688›Full record

ArticleBMJ open2024

Optimising HIV drug resistance testing laboratory networks in Kenya: insights from systems engineering modelling.

Yinsheng Wang, Leonard Kingwara, Anjuli Dawn Wagner, Nashon Yongo, Shukri A Hassan, Shan Liu, Patrick Oyaro, Rena C Patel

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2024. 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 42% 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, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Yinsheng WangDepartment of Industrial & Systems Engineering, University of Washington, Seattle, Washington, USA yinshw@uw.edu.ORCID 0009-0004-1735-8524
Leonard KingwaraNational HIV Reference Laboratory, Kenya Ministry of Health, Nairobi, Kenya.
Anjuli Dawn WagnerDepartment of Global Health, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-5851-1220
Nashon YongoUniversity of Washington Kenya Research and Training Center, Seattle, Washington, USA.
Shukri A HassanUniversity of Washington, Seattle, Washington, USA.
Shan LiuDepartment of Industrial and Systems Engineering, University of Washington, Seattle, Washington, USA.
Patrick OyaroHealth Innovations Kenya (HIK), Kisumu, Kenya.
Rena C PatelDepartment of Medicine, University of Washington, Seattle, Washington, USA.ORCID 0000-0001-9893-5856
University of Washington · USMinistry of Health · KE

Funding

Using systems science to optimize the impact of point-of-care viral load testing for pediatric HIV managementR21MH122361 · NIMH · UNIVERSITY OF WASHINGTON · PI PATEL, RENA CHIMAN, WAGNER, ANJULI DAWN · 2020 to 2021
$421k
NIMH NIH HHS R21 MH122361
6 · The paper itself

Abstract

backgroundHIV drug resistance (DR) is a growing threat to the durability of current and future HIV treatment success. DR testing (DRT) technologies are very expensive and specialised, relying on centralised laboratories in most low and middle-income countries. Modelling for laboratory network with point-of-care (POC) DRT assays to minimise turnaround time (TAT), is urgently needed to meet the growing demand.

methodsWe developed a model with user-friendly interface using integer programming and queueing theory to improve the DRT system in Kisumu County, Kenya. We estimated DRT demand based on both current and idealised scenarios and evaluated a centralised laboratory-only network and an optimised POC DRT network. A one-way sensitivity analysis of key user inputs was conducted.

resultsIn a centralised laboratory-only network, the mean TAT ranged from 8.52 to 8.55 working days, and the system could not handle a demand proportion exceeding 1.6%. In contrast, the mean TAT for POC DRT network ranged from 1.13 to 2.11 working days, with demand proportion up to 4.8%. Sensitivity analyses showed that expanding DRT hubs reduces mean TAT substantially while increasing the processing rate at national labs had minimal effect. For instance, doubling the current service rate at national labs reduced the mean TAT by only 0.0%-1.9% in various tested scenarios, whereas doubling the current service rate at DRT hubs reduced the mean TAT by 37.5%-49.8%. In addition, faster batching modes and transportation were important factors influencing the mean TAT.

conclusionsOur model offers decision-makers an informed framework for improving the DRT system using POC in Kenya. POC DRT networks substantially reduce mean TAT and can handle a higher demand proportion than a centralised laboratory-only network, especially for children and pregnant women living with HIV, where there is an immediate push to use DRT results for patient case management.

Indexed as

HIV InfectionsLaboratoriesChildEngineeringFemaleHumansKenyaPoint-of-Care SystemsPoint-of-Care TestingPregnancyDecision MakingHealth policyHIV & AIDS

Identifiers

PMID38569688
PMCPMC11146353
OpenAlexW4393853314

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.