Evidence map›Paper›PMID 38171495›Full record

ArticleBritish journal of haematology2024

Mental health, pain and likelihood of opioid misuse among adults with sickle cell disease.

Charles R Jonassaint, Ektha Parchuri, Julia A O'Brien, Christina M Lalama, Jonathan Lin, Sherif M Badawy, Megan E Hamm, Jennifer Stinson, Chitra Lalloo, C Patrick Carroll and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of haematology, 2024. 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
2.6field-weighted citation impact, top 11% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Chronic pain in the aging adult with sickle cell disease.Frontiers in pain research (Lausanne, Switzerland) · 2026
    Review
  2. Article
  3. Empowering sickle cell disease care: the rise ofFrontiers in rehabilitation sciences · 2024
    Article
  4. 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

20 authors at 11 institutions in 3 countries.

Charles R JonassaintDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-5662-5806
Ektha ParchuriDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0003-3862-3919
Julia A O'BrienDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-3208-3344
Christina M LalamaDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Jonathan LinDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Sherif M BadawyDepartment of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID 0000-0002-4739-265X
Megan E HammDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Jennifer StinsonChild Health Evaluative Sciences in Research Institute, Hospital for Sick Children and Lawrence S. Bloomberg, Faculty of Nursing, University of Toronto, Toronto, Ontario, Canada.
Chitra LallooChild Health Evaluation Sciences, Hospital for Sick Children, Toronto, Ontario, Canada.
C Patrick CarrollDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins Sickle Cell Center for Adults, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Santosh L SarafDepartment of Medicine, Sickle Cell Center, University of Illinois at Chicago, Chicago, Illinois, USA.ORCID 0000-0002-8584-4194
Victor R GordeukDepartment of Medicine, Sickle Cell Center, University of Illinois at Chicago, Chicago, Illinois, USA.ORCID 0000-0003-4725-7295
Robert CroninDepartment of Internal Medicine, Ohio State University, Columbus, Ohio, USA.
Nirmish ShahDivision of Hematology, Division of Pediatric Hematology/Oncology, Sickle Cell Transition Program, Duke University, Durham, North Carolina, USA.
Sophie M LanzkronDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins Sickle Cell Center for Adults, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Darla LilesDepartment of Internal Medicine, East Carolina University, Greenville, North Carolina, USA.ORCID 0000-0003-1480-7887
Cassandra TrimnellSickle Cell 101, San Jose, California, USA.
Lakiea BaileySickle Cell Community Consortium, Atlanta, Georgia, USA.
Raymona H LawrenceThe Jiann-Ping Hsu College of Public Health, Georgia Southern University in Statesboro, Statesboro, Georgia, USA.
Kaleab Z AbebeDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
University of Pittsburgh · USJohns Hopkins University · USUniversity of Illinois Chicago · USUniversity of Toronto · CACell Medica (Switzerland) · CHClinical Research Consortium · USDuke University · USEast Carolina University · USGeorgia Southern University · USNorthwestern University · USThe Ohio State University · US

Funding

Technology Research in Chronic & Critical IllnessT32NR008857 · NINR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Young Ji Lee · 2005 to 2026
$4.0M
Designing an Implementation Strategy for Delivering Routine Mental Health Screening and Treatment for Adolescents and Adults with Sickle Cell DiseaseR34MH125152 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JONASSAINT, CHARLES RICHARD · 2020 to 2021
$706k
NIMH NIH HHS R34 MH125152NINR NIH HHS T32 NR008857
6 · The paper itself

Abstract

Depressive symptoms are prevalent in individuals living with sickle cell disease (SCD) and may exacerbate pain. This study examines whether higher depressive symptoms are associated with pain outcomes, pain catastrophizing, interference and potential opioid misuse in a large cohort of adults with SCD. The study utilized baseline data from the 'CaRISMA' trial, which involved 357 SCD adults with chronic pain. Baseline assessments included pain intensity, daily mood, the Patient Health Questionnaire (PHQ), the Generalized Anxiety Disorders scale, PROMIS Pain Interference, Pain Catastrophizing Scale, the Adult Sickle Cell Quality of Life Measurement Information System and the Current Opioid Misuse Measure. Participants were categorized into 'high' or 'low' depression groups based on PHQ scores. Higher depressive symptoms were significantly associated with increased daily pain intensity, negative daily mood, higher pain interference and catastrophizing, poorer quality of life and a higher likelihood of opioid misuse (all p < 0.01). SCD patients with more severe depressive symptoms experienced poorer pain outcomes, lower quality of life and increased risk of opioid misuse. Longitudinal data from this trial will determine whether addressing depressive symptoms may potentially reduce pain frequency and severity in SCD.

Indexed as

Anemia, Sickle CellChronic PainOpioid-Related DisordersAdultHumansMental HealthQuality of LifeRandomized Controlled Trials as Topicdepressive symptomsecological momentary assessmenteHealthmental health, depressionmHealthpainquality of lifesickle cell disease

Identifiers

PMID38171495
PMCPMC10939903
OpenAlexW4390561560

What OpenQuestion holds

Textmetadata
LicenceTDM
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.