ArticleDrug and alcohol dependence2025
Trajectories of neighborhood-level overdose risk predictions for prioritization of harm reduction services: Results from the PROVIDENT study.
Article in Drug and alcohol dependence, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
backgroundNeighborhood-level overdose risk may vary over time. In Rhode Island, we developed and validated a machine learning model to identify the 20 percent of census block groups (CBGs) at the highest predicted risk of future overdose death. We updated this model periodically between November 2021 and August 2024 to generate six sets of predictions. This study aims to characterize the trajectory of each CBG's predicted overdose risk over time across these six periods.
methodsIn each prediction period, CBGs were designated as "high risk" or not designated as "high risk" based on our model's 20 percent predicted overdose risk threshold. We implemented sequence analysis to describe unique trajectories in each CBG's risk designation over each prediction period. We then calculated optimal matching distances to estimate dissimilarity between each pair of trajectories and applied agglomerative hierarchical clustering to group similar trajectories.
resultsThe 809 CBGs included in this study followed 60 unique trajectories in predicted overdose risk designation over the six prediction periods. Clustering of trajectories favored a solution with five trajectory groups. Most CBGs (73.4 %) were rarely or never designated as "high risk", 7.9 % of CBGs were always designated as "high risk", and the remaining 18.7 % were designated as "high risk" in multiple prediction periods, represented by trajectory groups with different patterning over time.
conclusionsGiven the substantial variability in which CBGs were at highest overdose risk over time, dynamic machine learning predictions may inform harm reduction resource allocation by identifying neighborhoods with emerging needs.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.