Evidence map›Paper›PMID 26355135›Full record

ReviewJournal of the American Board of Family Medicine : JABFM

Lessons Learned from Developing a Patient Engagement Panel: An OCHIN Report.

Jill Arkind, Sonja Likumahuwa-Ackman, Nate Warren, Kay Dickerson, Lynn Robbins, Kathy Norman, Jennifer E DeVoe

Registry-linked trialAbstract readReview
In one paragraph

Review in Journal of the American Board of Family Medicine : JABFM. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02298361 (Innovative Methods for Parents And Clinics to Create Tools), which is not on this 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.

NCT02298361 completednot on this map

Innovative Methods for Parents And Clinics to Create Tools (IMPACCT) for Kids' Care

TypeobservationalSponsorOCHIN, Inc.Ran2013 to 2016Enrolled27,251ConditionsInsurance Status/StabilityArmsHealth insurance outreach IT tools
3 · Its place in the literature

Who cites it

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

  1. Pooled it
  2. The Use of Arts-Based Methods to Enhance Patient Engagement in Health Research.Health expectations : an international journal of public participation in health care and health policy · 2024
    Review
  3. Article
  4. Article
  5. Partner-developed electronic health record tools to facilitate social risk-informed care planning.Journal of the American Medical Informatics Association : JAMIA · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Patient stakeholder engagement in research: A narrative review to describe foundational principles and best practice activities.Health expectations : an international journal of public participation in health care and health policy · 2019
    Review
  16. The Role of Participants in a Medical Information Commons.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2019
    Article
  17. Article
  18. Article
  19. Review
  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

7 authors.

Jill ArkindFrom OCHIN, Portland, OR (JA, NW, JED); Department of Family Medicine, Oregon Health & Science University, Portland (SL-A, JED); and the OCHIN Patient Engagement Panel (KD, Portland, Oregon; LR, Eureka, California; KN, Enterprise, Oregon).
Sonja Likumahuwa-AckmanFrom OCHIN, Portland, OR (JA, NW, JED); Department of Family Medicine, Oregon Health & Science University, Portland (SL-A, JED); and the OCHIN Patient Engagement Panel (KD, Portland, Oregon; LR, Eureka, California; KN, Enterprise, Oregon).
Nate WarrenFrom OCHIN, Portland, OR (JA, NW, JED); Department of Family Medicine, Oregon Health & Science University, Portland (SL-A, JED); and the OCHIN Patient Engagement Panel (KD, Portland, Oregon; LR, Eureka, California; KN, Enterprise, Oregon). warrenn@ochin.org.
Kay DickersonFrom OCHIN, Portland, OR (JA, NW, JED); Department of Family Medicine, Oregon Health & Science University, Portland (SL-A, JED); and the OCHIN Patient Engagement Panel (KD, Portland, Oregon; LR, Eureka, California; KN, Enterprise, Oregon).
Lynn RobbinsFrom OCHIN, Portland, OR (JA, NW, JED); Department of Family Medicine, Oregon Health & Science University, Portland (SL-A, JED); and the OCHIN Patient Engagement Panel (KD, Portland, Oregon; LR, Eureka, California; KN, Enterprise, Oregon).
Kathy NormanFrom OCHIN, Portland, OR (JA, NW, JED); Department of Family Medicine, Oregon Health & Science University, Portland (SL-A, JED); and the OCHIN Patient Engagement Panel (KD, Portland, Oregon; LR, Eureka, California; KN, Enterprise, Oregon).
Jennifer E DeVoeFrom OCHIN, Portland, OR (JA, NW, JED); Department of Family Medicine, Oregon Health & Science University, Portland (SL-A, JED); and the OCHIN Patient Engagement Panel (KD, Portland, Oregon; LR, Eureka, California; KN, Enterprise, Oregon).

Funding

CREATE Community CapacityRC4LM010852 · NLM · OREGON HEALTH & SCIENCE UNIVERSITY · PI SAULTZ, JOHN W · 2010 to 2010
$996k
NLM NIH HHS RC4 LM010852
6 · The paper itself

Abstract

There is renewed interest in patient engagement in clinical and research settings, creating a need for documenting and publishing lessons learned from efforts to meaningfully engage patients. This article describes early lessons learned from the development of OCHIN's Patient Engagement Panel (PEP). OCHIN supports a national network of more than 300 community health centers (CHCs) and other primary care settings that serve over 1.5 million patients annually across nearly 20 states. The PEP was conceived in 2009 to harness the CHC tradition of patient engagement in this new era of patient-centered outcomes research and to ensure that patients were engaged throughout the life cycle of our research projects, from conception to dissemination. Developed by clinicians and researchers within our practice-based research network, recruitment of patients to serve as PEP members began in early 2012. The PEP currently has a membership of 18 patients from 3 states. Over the past 24 months, the PEP has been involved with 12 projects. We describe developing the PEP and challenges and lessons learned (eg, recruitment, funding model, creating value for patient partners, compensation). These lessons learned are relevant not only for research but also for patient engagement in quality improvement efforts and other clinical initiatives.

Indexed as

Community Health CentersCooperative BehaviorElectronic Health RecordsHealth Services ResearchHumansPatient ParticipationPatient-Centered Outcomes ResearchPatient EngagementPopulationsPrimary Health CareUnderserved

Identifiers

PMID26355135
PMCPMC4904782

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.