Evidence map›Paper›PMID 23343879›Full record

ArticlePain management nursing : official journal of the American Society of Pain Management Nurses2014

Care seeking for pain in young adults with sickle cell disease.

Coretta M Jenerette, Cheryl A Brewer, Kenneth I Ataga

Abstract read
In one paragraph

Article in Pain management nursing : official journal of the American Society of Pain Management Nurses, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Stigma of Sickle Cell Disease: A Systematic Review.Issues in mental health nursing · 2018
    Pooled it
  2. Trial
  3. Feasibility of In-Home Virtual Reality for Chronic Pain in Sickle Cell Disease.Pain management nursing : official journal of the American Society of Pain Management Nurses · 2024
    Trial
  4. Chronic pain in the aging adult with sickle cell disease.Frontiers in pain research (Lausanne, Switzerland) · 2026
    Review
  5. Provider Implicit Racial Bias in Pediatric Sickle Cell Disease.Journal of racial and ethnic health disparities · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Individuals with Sickle Cell Disease Using SBAR as a Communication Tool: A Pilot Study.International journal of environmental research and public health · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Understanding the Self-Management Practices of Young Adults with Sickle Cell Disease.Journal of sickle cell disease and hemoglobinopathies · 2017
    Article
  18. Article
  19. Does Attendance at a Sickle Cell Educational Conference Improve Clinician Knowledge and Attitude Toward Patients with Sickle Cell Disease?Pain management nursing : official journal of the American Society of Pain Management Nurses · 2016
    Article
  20. 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

3 authors.

Coretta M JeneretteSchool of Nursing, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina. Electronic address: coretta.jenerette@unc.edu.
Cheryl A BrewerDuke Cancer Care Research Program, Duke Cancer Institute, Durham, North Carolina.
Kenneth I AtagaDivision of Hematology/Oncology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Funding

Decreasing Health-Related Stigma in Adults with Sickle Cell DiseaseK23NR011061 · NINR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JENERETTE, CORETTA M. · 2009 to 2011
$359k
NINR NIH HHS K23 NR011061NINR NIH HHS K23NR011061
6 · The paper itself

Abstract

In individuals with sickle cell disease (SCD), recognizing the cues to an acute pain episode and responding appropriately are important. The purpose of this mixed-methods pilot study is to identify preliminary factors that influence care seeking for pain in young adults with SCD. Responses were received from 69 young adults with SCD, age 18-35 years. The majority of respondents (88%) wait until the pain intensity is an average of 8.7 (± 1.2) on a scale of 1 to 10 before seeking care. Prominent themes influencing care seeking for pain include: trying to treat pain at home, avoiding the emergency department because of past treatment experiences, the desire to avoid admission to the hospital, and the importance of time in the lives of the young adults with SCD. Young adults with SCD need additional support from family and healthcare providers in order to make timely, appropriate decisions regarding care seeking.

Indexed as

AdolescentAdultAnemia, Sickle CellAttitude to HealthFemaleHospitalizationHumansMalePainPain ManagementPatient Acceptance of Health CarePilot ProjectsQualitative ResearchSelf CareTime-to-TreatmentYoung Adult

Identifiers

PMID23343879
PMCPMC3742711

What OpenQuestion holds

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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.