Evidence map›Paper›PMID 32542189›Full record

ArticleJournal of psychiatry and brain science2020

The Prescription Opioids and Depression Pathways Cohort Study.

Jeffrey F Scherrer, Brian Ahmedani, Kirsti Autio, Lynn Debar, Patrick J Lustman, Lisa R Miller-Matero, Joanne Salas, Scott Secrest, Mark D Sullivan, Lauren Wilson and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of psychiatry and brain science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 20 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

11 authors at 1 institution in 1 country.

Jeffrey F ScherrerDepartment of Family and Community Medicine, Saint Louis University School of Medicine, 1402 South Grand Blvd, St. Louis, MO 63104, USA.
Brian AhmedaniCenter for Health Policy and Health Services Research and Behavioral Health Services, Henry Ford Health System, One Ford Place, Detroit, MI 48202, USA.
Kirsti AutioCenter for Health Policy and Health Services Research and Behavioral Health Services, Henry Ford Health System, One Ford Place, Detroit, MI 48202, USA.
Lynn DebarKaiser Permanente Washington Health Research Institute, 1730 Minor Ave, Seattle, WA 98101, USA.
Patrick J LustmanDepartment of Psychiatry, Washington University School of Medicine, 660 South Euclid Ave. St. Louis, MO 63110, USA.
Lisa R Miller-MateroCenter for Health Policy and Health Services Research and Behavioral Health Services, Henry Ford Health System, One Ford Place, Detroit, MI 48202, USA.
Joanne SalasDepartment of Family and Community Medicine, Saint Louis University School of Medicine, 1402 South Grand Blvd, St. Louis, MO 63104, USA.
Scott SecrestDepartment of Family and Community Medicine, Saint Louis University School of Medicine, 1402 South Grand Blvd, St. Louis, MO 63104, USA.
Mark D SullivanDepartment of Psychiatry and Behavioral Science, University of Washington School of Medicine, Seattle, WA 98195, USA.
Lauren WilsonDepartment of Family and Community Medicine, Saint Louis University School of Medicine, 1402 South Grand Blvd, St. Louis, MO 63104, USA.
Sarah Skiold-HanlinDepartment of Family and Community Medicine, Saint Louis University School of Medicine, 1402 South Grand Blvd, St. Louis, MO 63104, USA.
Kaiser Permanente Washington Health Research Institute · US

Funding

Pathways from Chronic Prescription Opioid Use to New Onset Mood DisorderR01DA043811 · NIDA · SAINT LOUIS UNIVERSITY · PI SCHERRER, JEFFREY F. · 2019 to 2023
$3.2M
NIDA NIH HHS R01 DA043811
6 · The paper itself

Abstract

backgroundResults from studies using medical record data indicate chronic (>90 days) opioid analgesic use (OAU) is associated with new depressive episodes (NDE), worsening depression and risk for depression recurrence. This body of evidence is based on retrospective cohort studies and medical record data. Limitations of existing research are overcome in a new prospective cohort study of the opioid-depression relationship.

methodsProspective cohort of 1500 adult patients recruited from two health care systems. Eligible subjects started a new period of OAU and have 30 to 90 days of OAU at baseline. Diagnostic assessments for psychiatric disorders, structured measures of pain, pain functioning, opioid use, social support, sleep and impulsivity will be obtained at baseline, 6-month and 12-month follow-up. Baseline participants will be invited to 12 monthly brief assessments of pain-related functioning, depression symptoms and opioid use. INNOVATION: Robust control for confounding by indication and detailed phenotyping of depression and opioid use disorder. ANTICIPATED

resultsChronic OAU will be associated with new onset of a depression phenotype characterized by anhedonia and somatic symptoms. This relationship will be partly, but not completely explained by impaired functioning and low social support.

conclusionsAlthough the annual number of opioid prescriptions in the United States has decreased, over 190 million patients have OAU each year. If chronic OAU leads to a clinically meaningful affective disorder, independent of pain, then we need to consider depression an important adverse effect of chronic OAU and adjust care for chronic pain accordingly.

Indexed as

anxietydepressionepidemiologyhealth related quality of lifeopioidspainsleepsocial supportsubstance use disorder

Identifiers

PMID32542189
PMCPMC7295174
OpenAlexW3023723276

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.