Evidence map›Paper›PMID 39010038›Full record

ArticleBMC public health2024

Risk factors for persistent fatal opioid-involved overdose clusters in Massachusetts 2011-2021: a spatial statistical analysis with socio-economic, accessibility, and prescription factors.

Sumeeta Srinivasan, Jennifer Pustz, Elizabeth Marsh, Leonard D Young, Thomas J Stopka

Abstract read
In one paragraph

Article in BMC public health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
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  4. Article
  5. Spatiotemporal Analysis of Fentanyl-Associated Overdose Deaths in Chicago, IL, USA.Journal of urban health : bulletin of the New York Academy of Medicine · 2025
    Article
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sumeeta SrinivasanDepartment of Urban and Environmental Policy and Planning, Tufts University, Medford, MA, USA. sumeeta.srinivasan@tufts.edu.
Jennifer PustzDepartment of Public Health and Community Medicine, Tufts University School of Medicine, Boston, MA, USA.
Elizabeth MarshInstitute for Health Metrics and Evaluation, Seattle, WA, USA.
Leonard D YoungPrescription Monitoring Program, Massachusetts Department of Public Health, Boston, MA, USA.
Thomas J StopkaDepartment of Public Health and Community Medicine, Tufts University School of Medicine, Boston, MA, USA.

Funding

CDC and MDPH INTF7311HH2 500224100 (PI: Stopka)
6 · The paper itself

Abstract

backgroundFatal opioid-involved overdose rates increased precipitously from 5.0 per 100,000 population to 33.5 in Massachusetts between 1999 and 2022.

methodsWe used spatial rate smoothing techniques to identify persistent opioid overdose-involved fatality clusters at the ZIP Code Tabulation Area (ZCTA) level. Rate smoothing techniques were employed to identify locations of high fatal opioid overdose rates where population counts were low. In Massachusetts, this included areas with both sparse data and low population density. We used Local Indicators of Spatial Association (LISA) cluster analyses with the raw incidence rates, and the Empirical Bayes smoothed rates to identify clusters from 2011 to 2021. We also estimated Empirical Bayes LISA cluster estimates to identify clusters during the same period. We constructed measures of the socio-built environment and potentially inappropriate prescribing using principal components analysis. The resulting measures were used as covariates in Conditional Autoregressive Bayesian models that acknowledge spatial autocorrelation to predict both, if a ZCTA was part of an opioid-involved cluster for fatal overdose rates, as well as the number of times that it was part of a cluster of high incidence rates.

resultsLISA clusters for smoothed data were able to identify whether a ZCTA was part of a opioid involved fatality incidence cluster earlier in the study period, when compared to LISA clusters based on raw rates. PCA helped in identifying unique socio-environmental factors, such as minoritized populations and poverty, potentially inappropriate prescribing, access to amenities, and rurality by combining socioeconomic, built environment and prescription variables that were highly correlated with each other. In all models except for those that used raw rates to estimate whether a ZCTA was part of a high fatality cluster, opioid overdose fatality clusters in Massachusetts had high percentages of Black and Hispanic residents, and households experiencing poverty. The models that were fitted on Empirical Bayes LISA identified this phenomenon earlier in the study period than the raw rate LISA. However, all the models identified minoritized populations and poverty as significant factors in predicting the persistence of a ZCTA being part of a high opioid overdose cluster during this time period.

conclusionConducting spatially robust analyses may help inform policies to identify community-level risks for opioid-involved overdose deaths sooner than depending on raw incidence rates alone. The results can help inform policy makers and planners about locations of persistent risk.

Indexed as

Bayes TheoremOpiate OverdoseSocioeconomic FactorsSpatial AnalysisAdultAnalgesics, OpioidCluster AnalysisDrug OverdoseFemaleHealth Services AccessibilityHumansMaleMassachusettsRisk FactorsAnalgesics, OpioidBuilt environmentEmpirical bayes LISAEmpirical bayes smoothingLocal Indicators of Spatial Association (LISA) clustersOpioid deathOpioidsOverdosePublic healthSocial determinants of healthSpatial statistics

Identifiers

PMID39010038
PMCPMC11251103

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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.