Evidence map›Paper›PMID 29885157›Full record

ArticleJournal of studies on alcohol and drugs2018

Latent Classes of Polydrug Users as a Predictor of Crash Involvement and Alcohol Consumption.

Michael Scherer, Eduardo Romano, Robert Voas, Eileen Taylor

Abstract read
In one paragraph

Article in Journal of studies on alcohol and drugs, 2018. 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
–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

The trial behind it

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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.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Michael SchererPacific Institute for Research and Evaluation, Calverton, Maryland.
Eduardo RomanoPacific Institute for Research and Evaluation, Calverton, Maryland.
Robert VoasPacific Institute for Research and Evaluation, Calverton, Maryland.
Eileen TaylorPacific Institute for Research and Evaluation, Calverton, Maryland.

Funding

Drivers with Alcohol Use Disorders: At high risk for crashes?R01AA018352 · NIAAA · PACIFIC INSTITUTE FOR RES AND EVALUATION · PI VOAS, ROBERT B · 2009 to 2010
$1.0M
NIAAA NIH HHS R01 AA018352
6 · The paper itself

Abstract

objectivePolydrug users have been shown to be at higher risk for alcohol consumption and crash involvement. However, research has shown that polydrug groups differ in some important ways. It is currently unknown how polydrug-using groups differ in terms of crash involvement and alcohol consumption.

methodThe current study used latent class analysis to examine subgroups of polydrug users (n = 384) among a sample of drivers in Virginia Beach, Virginia (N = 10,512). A series of logistic regression analyses were conducted to determine the relationship between polydrug use categories and crash involvement and alcohol consumption.

resultsFour distinct subclasses of users were identified among polydrug-using drivers: Class 1 is the "marijuana-amphetamines class" and accounts for 21.6% of polydrug users. Class 2 is the "benzo-antidepressant class" and accounts for 39.0% of polydrug users. Class 3 is the "opioid-benzo class" and accounts for 32.7% of polydrug users. Finally, Class 4 is the "marijuana-cocaine class" and accounts for 6.7% of the study sample. Drivers in the opioid-benzo class were significantly more likely than those in any other class as well as non-drug users and single-drug users to be involved in a crash and were more likely than those in most other conditions to consume alcohol. No significant difference was found between marijuana-amphetamine users or benzo-antidepressant users and non-drug users on crash risk.

conclusionsSome polydrug users are indeed at greater risk for crash involvement and alcohol consumption; however, not all polydrug users are significantly worse than single-drug users and/or non-drug users, and the practice of lumping polydrug users together when predicting crash risk runs the risk of inaccurately attributing crash involvement to certain drivers.

Indexed as

Accidents, TrafficAlcohol DrinkingAnalgesics, OpioidDrug UsersFemaleHumansMaleSubstance-Related DisordersVirginiaAnalgesics, Opioid

Identifiers

PMID29885157
PMCPMC6005252

What OpenQuestion holds

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Registered trials

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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.