Evidence map›Paper›PMID 36289563›Full record

ArticleJournal of the American Geriatrics Society2023

High opioid doses, naloxone, and central nervous system active medications received by Medicare-enrolled adults.

Armando Silva Almodóvar, Milap C Nahata

Open access · hybridAbstract read
In one paragraph

Article in Journal of the American Geriatrics Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

2 authors at 1 institution in 1 country.

Armando Silva AlmodóvarCollege of Pharmacy, Institute of Therapeutic Innovations and Outcomes (ITIO), The Ohio State University, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0002-9601-9413
Milap C NahataCollege of Pharmacy, Institute of Therapeutic Innovations and Outcomes (ITIO), The Ohio State University, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0003-1936-0666
The Ohio State University · US

Funding

U.S. Deprescribing Research NetworkR24AG064025 · NIA · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI BOYD, CYNTHIA MELINDA, STEINMAN, MICHAEL A. · 2019 to 2023
$9.9M
Avatar FoundationNIA NIH HHS R24 AG064025NIA NIH HHS R24AG064025
6 · The paper itself

Abstract

backgroundA limited number of studies have analyzed prescribing among Medicare-enrolled adults at risk for opioid overdoses. The objectives of this study were to evaluate prescribing for naloxone and central nervous system (CNS) active medications and to determine the relationships of patient characteristics with exposure to these medications.

methodsThis was a retrospective cross-sectional analysis of a Medicare-enrolled medication therapy management eligible cohort. Patients were stratified into two cohorts, individuals with a mean daily morphine milligram equivalent (MME) dose <50 and individuals with MME ≥50. Medications assessed included benzodiazepines, skeletal muscle relaxants (SMR), hypnotics, gabapentanoids, selective-serotonin reuptake inhibitors (SSRI), serotonin-norepinephrine reuptake inhibitors (SNRI), tricyclic antidepressants (TCA), antipsychotics, barbiturates, other antiepileptics, hydroxyzine, and naloxone. Chi-square with odds ratios and logistic regressions determined the relationships of medications and patient characteristics with mean daily MME ≥50. Relationship between medications and opioid dose was adjusted for age and sex.

resultsThere were 3452 patients with a daily MME <50 and 1116 with a daily MME ≥50. After adjusting for age and sex, patients with a daily MME ≥50 were more likely to be prescribed hypnotics (OR: 1.41, 95% CI 1.17-1.70), SNRIs (OR: 1.39, 95% CI 1.17-1.64), and naloxone (OR: 3.21, 95% CI 2.49-4.12) (p < 0.001). Nine percent of eligible patients received naloxone. Age groups of persons <85 years of age had 1.58-4.04 (p ≤ 0.004) times the odds of being prescribed a mean daily MME ≥50.

conclusionNearly one-fourth of patients were prescribed a mean daily opioid therapy of MME ≥50. These patients were more likely to be prescribed hypnotics, SNRIs, and naloxone. Patients receiving chronic high-dose opioid therapy were more likely to be in age groups of persons <85 years. Naloxone may be underprescribed among eligible adults. Targeted medication services may ensure optimal prescribing among Medicare patients with chronic opioid therapies.

Indexed as

Analgesics, OpioidSerotonin and Noradrenaline Reuptake InhibitorsAgedAged, 80 and overCentral Nervous SystemCentral Nervous System AgentsCross-Sectional StudiesEndrinHumansHypnotics and SedativesMedicareNaloxonePractice Patterns, Physicians'Retrospective StudiesSelective Serotonin Reuptake InhibitorsUnited StatesAnalgesics, OpioidCentral Nervous System AgentsEndrinHypnotics and SedativesMMENaloxoneSelective Serotonin Reuptake InhibitorsSerotonin and Noradrenaline Reuptake Inhibitorscentral nervous system active medicationchronic usedrug interactionsMedicaremedication therapy managementnaloxoneopioid

Identifiers

PMID36289563
PMCPMC9870936
OpenAlexW4307431400

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.