Evidence map›Paper›PMID 32913937›Full record

ArticleInfectious Disease Modelling2020

Contribution of high risk groups' unmet needs may be underestimated in epidemic models without risk turnover: A mechanistic modelling analysis.

Jesse Knight, Stefan D Baral, Sheree Schwartz, Linwei Wang, Huiting Ma, Katherine Young, Harry Hausler, Sharmistha Mishra

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Article in Infectious Disease Modelling, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jesse KnightMAP Centre for Urban Health Solutions, Unity Health Toronto, Canada.
Stefan D BaralDeptartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, USA.
Sheree SchwartzDeptartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, USA.
Linwei WangMAP Centre for Urban Health Solutions, Unity Health Toronto, Canada.
Huiting MaMAP Centre for Urban Health Solutions, Unity Health Toronto, Canada.
Katherine YoungTB HIV Care, South Africa.
Harry HauslerTB HIV Care, South Africa.
Sharmistha MishraMAP Centre for Urban Health Solutions, Unity Health Toronto, Canada.

Funding

Examining PrEP use, implementation preferences and the potential for social support to improve PrEP delivery and persistence among female sex workers in Durban, South AfricaR01NR016650 · NINR · JOHNS HOPKINS UNIVERSITY · PI BARAL, STEFAN DAVID · 2016 to 2020
$3.2M
NINR NIH HHS R01 NR016650
6 · The paper itself

Abstract

backgroundEpidemic models of sexually transmitted infections (STIs) are often used to characterize the contribution of risk groups to overall transmission by projecting the transmission population attributable fraction (tPAF) of unmet prevention and treatment needs within risk groups. However, evidence suggests that STI risk is dynamic over an individual's sexual life course, which manifests as turnover between risk groups. We sought to examine the mechanisms by which turnover influences modelled projections of the tPAF of high risk groups.

methodsWe developed a unifying, data-guided framework to simulate risk group turnover in deterministic, compartmental transmission models. We applied the framework to an illustrative model of an STI and examined the mechanisms by which risk group turnover influenced equilibrium prevalence across risk groups. We then fit a model with and without turnover to the same risk-stratified STI prevalence targets and compared the inferred level of risk heterogeneity and tPAF of the highest risk group projected by the two models.

resultsThe influence of turnover on group-specific prevalence was mediated by three main phenomena: movement of previously high risk individuals with the infection into lower risk groups; changes to herd effect in the highest risk group; and changes in the number of partnerships where transmission can occur. Faster turnover led to a smaller ratio of STI prevalence between the highest and lowest risk groups. Compared to the fitted model without turnover, the fitted model with turnover inferred greater risk heterogeneity and consistently projected a larger tPAF of the highest risk group over time. IMPLICATIONS: If turnover is not captured in epidemic models, the projected contribution of high risk groups, and thus, the potential impact of prioritizing interventions to address their needs, could be underestimated. To aid the next generation of tPAF models, data collection efforts to parameterize risk group turnover should be prioritized.

Indexed as

HIV, human immunodeficiency virusMathematical modellingPopulation attributable fractionRisk heterogeneitySexually transmitted infectionSTI, sexually transmitted infectiontPAF, transmission population attributable fractionTransmissionTurnover

Identifiers

PMID32913937
PMCPMC7452422

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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.