Evidence map›Paper›PMID 35191022›Full record

ArticleBiometrics2023

A hierarchical model for analyzing multisite individual-level disease surveillance data from multiple systems.

Yuzi Zhang, Howard H Chang, Qu Cheng, Philip A Collender, Ting Li, Jinge He, Justin V Remais

Open access · greenAbstract read
In one paragraph

Article in Biometrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Yuzi ZhangDepartment of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, USA.ORCID 0000-0003-1805-6910
Howard H ChangDepartment of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-6316-1640
Qu ChengDivision of Environmental Health Sciences, University of California, Berkeley, California, USA.
Philip A CollenderDivision of Environmental Health Sciences, University of California, Berkeley, California, USA.
Ting LiInstitute of Tuberculosis Control and Prevention, Sichuan Center for Disease Control and Prevention, Chengdu, Sichuan, China.
Jinge HeInstitute of Tuberculosis Control and Prevention, Sichuan Center for Disease Control and Prevention, Chengdu, Sichuan, China.
Justin V RemaisDivision of Environmental Health Sciences, University of California, Berkeley, California, USA.
University of California, Berkeley · USEmory University · USSichuan Center for Disease Control and Prevention · CN

Funding

Spatio-temporal data integration methods for infectious disease surveillanceR01AI125842 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI CHANG, HOWARD H, REMAIS, JUSTIN V · 2017 to 2021
$3.6M
Effects of agricultural expansion and intensification on infectionsR01TW010286 · FIC · UNIVERSITY OF SOUTH FLORIDA · PI REMAIS, JUSTIN V, ROHR, JASON ROBERT · 2015 to 2019
$2.4M
FIC NIH HHS R01 TW010286NIAID NIH HHS R01 AI125842
6 · The paper itself

Abstract

Passive surveillance systems are widely used to monitor diseases occurrence over wide spatial areas due to their cost-effectiveness and integration into broadly distributed healthcare systems. However, such systems are generally associated with imperfect ascertainment of disease cases and with heterogeneous capture probabilities arising from factors such as differential access to care. Augmenting passive surveillance systems with other surveillance efforts provides a way to estimate the true number of incident cases. We develop a hierarchical modeling framework for analyzing data from multiple surveillance systems that allows for individual-level covariate-dependent heterogeneous capture probabilities, and borrows information across surveillance sites to improve estimation of the true number of incident cases. Inference is carried out via a two-stage Bayesian procedure. Simulation studies illustrated superior performance of the proposed approach with respect to bias, root mean square error, and coverage compared to a model that does not borrow information across sites. We applied the proposed model to data from three surveillance systems reporting pulmonary tuberculosis (PTB) cases in a major center of ongoing transmission in China. The analysis yielded bias-corrected estimates of PTB cases from the passive system and led to the identification of risk factors associated with PTB rates, as well as factors influencing the operating characteristics of the implemented surveillance systems.

Indexed as

Public Health SurveillanceBayes TheoremComputer SimulationData AnalysisHumansRisk FactorsTuberculosis, PulmonaryBayesian hierarchical modelingheterogeneous capture probabilitiesindividual-level disease surveillance

Identifiers

PMID35191022
PMCPMC10027420
OpenAlexW4213152513

What OpenQuestion holds

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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.