Evidence map›Paper›PMID 36203857›Full record

ArticlePLOS digital health2022

Prescription quantity and duration predict progression from acute to chronic opioid use in opioid-naïve Medicaid patients.

Drake G Johnson, Vy Thuy Ho, Jennifer M Hah, Keith Humphreys, Ian Carroll, Catherine Curtin, Steven M Asch, Tina Hernandez-Boussard

Open access · goldAbstract read
In one paragraph

Article in PLOS digital health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
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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

8 authors at 1 institution in 1 country.

Drake G JohnsonDepartment of Medicine, Stanford University, Stanford California, United States of America.ORCID 0000-0001-9466-880X
Vy Thuy HoDepartment of Surgery, Stanford University, Stanford California, United States of America.ORCID 0000-0002-5570-0536
Jennifer M HahDepartment of Anesthesiology, Perioperative, and Pain Medicine, Stanford University, Stanford California, United States of America.ORCID 0000-0002-9739-3968
Keith HumphreysDepartment of Psychiatry, Stanford University, Stanford California, United States of America.
Ian CarrollDepartment of Anesthesiology, Perioperative, and Pain Medicine, Stanford University, Stanford California, United States of America.ORCID 0000-0002-4777-4834
Catherine CurtinDepartment of Surgery, Stanford University, Stanford California, United States of America.
Steven M AschDepartment of Medicine, Stanford University, Stanford California, United States of America.
Tina Hernandez-BoussardDepartment of Medicine, Stanford University, Stanford California, United States of America.ORCID 0000-0001-6553-3455
Stanford University · US

Funding

Advancing Knowledge Discovery for Postoperative Pain ManagementR01LM013362 · NLM · STANFORD UNIVERSITY · PI HERNANDEZ-BOUSSARD, TINA · 2019 to 2023
$3.2M
NLM NIH HHS R01 LM013362
6 · The paper itself

Abstract

Opiates used for acute pain are an established risk factor for chronic opioid use (COU). Patient characteristics contribute to progression from acute opioid use to COU, but most are not clinically modifiable. To develop and validate machine-learning algorithms that use claims data to predict progression from acute to COU in the Medicaid population, Adult opioid naïve Medicaid patients from 6 anonymized states who received an opioid prescription between 2015 and 2019 were included. Five machine learning (ML) Models were developed, and model performance assessed by area under the receiver operating characteristic curve (auROC), precision and recall. In the study, 29.9% (53820/180000) of patients transitioned from acute opioid use to COU. Initial opioid prescriptions in COU patients had increased morphine milligram equivalents (MME) (33.2 vs. 23.2), tablets per prescription (45.6 vs. 36.54), longer prescriptions (26.63 vs 24.69 days), and higher proportions of tramadol (16.06% vs. 13.44%) and long acting oxycodone (0.24% vs 0.04%) compared to non- COU patients. The top performing model was XGBoost that achieved average precision of 0.87 and auROC of 0.63 in testing and 0.55 and 0.69 in validation, respectively. Top-ranking prescription-related features in the model included quantity of tablets per prescription, prescription length, and emergency department claims. In this study, the Medicaid population, opioid prescriptions with increased tablet quantity and days supply predict increased risk of progression from acute to COU in opioid-naïve patients. Future research should evaluate the effects of modifying these risk factors on COU incidence.

Identifiers

PMID36203857
PMCPMC9534483
OpenAlexW4293253506

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

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.