Evidence map›Paper›PMID 42696281›Full record

ArticleJAMA network open2026

Opioid Dispensing Volume and Per-Patient Intensity in Sickle Cell Disease.

Kevin Y Xu, Brandon K Attell, Joanna L Buss, Tashalee R Brown, Charles R Jonassaint, Richard A Grucza, Allison A King, Max Jordan Nguemeni Tiako

Abstract read
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kevin Y XuDepartment of Psychiatry, Washington University School of Medicine, St Louis, Missouri.
Brandon K AttellGeorgia Health Policy Center, Georgia State University, Atlanta.
Joanna L BussCenter for Advancing Health Services, Policy & Economics Research, Washington University, St Louis, Missouri.
Tashalee R BrownDepartment of Psychiatry, University of California Los Angeles David Geffen School of Medicine, Los Angeles.
Charles R JonassaintDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia.
Richard A GruczaDepartment of Family and Community Medicine, Saint Louis University School of Medicine, St Louis, Missouri.
Allison A KingWashington University School of Public Health, St Louis, Missouri.
Max Jordan Nguemeni TiakoDepartment of Medicine, University of California Los Angeles David Geffen School of Medicine, Los Angeles.

Funding

UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
The Center for Health Improvement of Minority ElderlyP30AG021684 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CATHERINE A SARKISIAN · 2002 to 2026
$19.7M
PHARMacist and Community Health Support to Optimize Medications After Trauma Surgery (PHARM-C)P50MH122351 · NIMH · WASHINGTON UNIVERSITY · PI Joanna Abraham · 2021 to 2026
$10.8M
Peer suppoRt for adolescents and Emerging adults with Sickle cell pain: promoting ENgagement in Cognitive behavioral thErapyUG3HL165839 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI COLVIN, ALICIA, JONASSAINT, CHARLES RICHARD · 2023 to 2023
$819k
Using Big Data to Optimize Treatment of Opioid Use Disorder in PregnancyK08DA061258 · NIDA · WASHINGTON UNIVERSITY · PI Kevin Young Xu · 2024 to 2026
$664k
NCATS NIH HHS UL1 TR001881NCATS NIH HHS UL1 TR002345NCBDD CDC HHS U01 DD000037NHLBI NIH HHS UG3 HL165839NIA NIH HHS P30 AG021684NIDA NIH HHS K08 DA061258NIMH NIH HHS P50 MH122351
6 · The paper itself

Abstract

Importance: Opioids remain central to management of acute and chronic pain in sickle cell disease (SCD). Opioid dispensing declined over the 2010s amid opioid stewardship efforts, but patterns since 2020 are less clear. Analyses aggregating opioids into morphine milligram equivalents (MME) may obscure agent-specific patterns. Objective: To characterize opioid dispensing volume and per-recipient frequency, duration, and dose among individuals with SCD. Design, Setting, and Participants: A retrospective cohort study of commercially insured and Medicaid-enrolled patients with SCD using the Merative MarketScan databases across 3 periods from January 2011 to February 2016, March 2016 to December 2020, and January 2021 to December 2023. Exposure: Calendar time across 3 prespecified periods: January 2011 to February 2016, March 2016 to December 2020, and January 2021 to December 2023. Main Outcomes and Measures: Changes in opioid dispensing were examined across 3 periods (January 2011 to February 2016, March 2016 to December 2020, and January 2021 to December 2023). Segmented regression models estimated monthly percentage changes (MPCs) in 4 outcomes: (1) total dispensed prescriptions per 100 enrollees; and, among enrollees receiving opioids, (2) mean prescriptions per person, (3) mean days supplied, and (4) mean daily MMEs. Analyses included 6 opioids (hydromorphone, hydrocodone, morphine, tramadol, oxycodone, methadone) stratified by insurance type (commercial vs Medicaid). Results: Across 48 760 individuals with SCD contributing person-time, 24 692 (50.6%) were Medicaid beneficiaries, 20 969 (43.0%) were aged 19 to 40 years, and 29 380 (60.3%) were female. From January 2021 through December 2023, total dispensing increased for all 6 agents among Medicaid beneficiaries, with the largest monthly increases for methadone (MPC, 1.76%; 95% CI, 1.24% to 2.29%) and hydromorphone (MPC, 1.43%; 95% CI, 1.00% to 1.86%). Among commercial enrollees, total dispensing increased for oxycodone (MPC, 0.84%; 95% CI, 0.60% to 1.07%) and morphine (MPC, 0.87%; 95% CI, 0.42% to 1.33%), was stable for hydrocodone, hydromorphone, and methadone, and declined for tramadol (MPC, -0.79%; 95% CI, -1.16% to -0.42%). Dispensed prescriptions increased only for oxycodone among commercially insured individuals (MPC, 0.14%; 95% CI, 0.08% to 0.20%) and tramadol among those with Medicaid (MPC, 0.96%; 95% CI, 0.56% to 1.36%). Mean days supplied and mean daily MMEs did not significantly increase for any opioid-insurance combination. Conclusions and Relevance: Among individuals with SCD, total opioid dispensing increased or stabilized during 2021 to 2023 after prior declines, most prominently among Medicaid beneficiaries, without broad increases in per-recipient frequency, duration, or dose. These patterns are consistent with broader distribution of opioid dispensing rather than treatment intensification among recipients.

Indexed as

Analgesics, OpioidAnemia, Sickle CellChronic PainDrug PrescriptionsPractice Patterns, Physicians'AdultFemaleHumansHydrocodoneMaleMedicaidRetrospective StudiesUnited StatesAnalgesics, OpioidHydrocodone

Identifiers

PMID42696281
PMCPMC13629608

What Socratic holds

Textmetadata
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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 Socratic graph.