Evidence map›Paper›PMID 40487468›Full record

ArticleACI open2024

Stakeholder Perspectives on the Meaningful Integration of Clinical Informatics Interventions Using Patient-Reported Outcomes in Healthcare.

David Russell, Yashika Sharma, Andrew P Ambrosy, Kelly Axsom, Janejira J Chaiyasit, Margaret O Cuomo, Christi Deaton, Anne J Goldberg, Parag Goyal, Angel Guan and 7 more

Abstract read
In one paragraph

Article in ACI open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

17 authors.

David RussellDepartment of Sociology, Appalachian State University, Boone, North Carolina, United States.
Yashika SharmaColumbia University School of Nursing, New York, New York, United States.
Andrew P AmbrosyDepartment of Cardiology, Kaiser Permanente San Francisco Medical Center, San Francisco, California, United States.
Kelly AxsomColumbia University Vagelos College of Physicians and Surgeons, New York, New York, United States.
Janejira J ChaiyasitUniversity of Cambridge School of Clinical Medicine, Cambridge, United Kingdom.
Margaret O CuomoColumbia University Vagelos College of Physicians and Surgeons, New York, New York, United States.
Christi DeatonColumbia University Vagelos College of Physicians and Surgeons, New York, New York, United States.
Anne J GoldbergColumbia University School of Nursing, New York, New York, United States.
Parag GoyalWeill Cornell Medicine, New York, New York, United States.
Angel GuanColumbia University School of Nursing, New York, New York, United States.
Fernanda C G PolubriaginofMemorial Sloan Kettering Cancer Center, New York, New York, United States.
Lucy McGurkDepartment of Sociology, Appalachian State University, Boone, North Carolina, United States.
Alexander T SandhuDivision of Cardiology and Stanford Prevention Research Center, Department of Medicine, Stanford University School of Medicine, Stanford, California, United States.
John A SpertusUniversity of Missouri - Kansas City's Healthcare Institute for Innovations in Quality and Saint Luke's Mid America Health Institute, Kansas City, Missouri, United States.
Meghan Reading TurchioeColumbia University School of Nursing, New York, New York, United States.
David K VawdreyGeisinger, Danville, Pennsylvania, United States.
Ruth Masterson CreberColumbia University School of Nursing, New York, New York, United States.

Funding

Improve the Meaning of Patient Reported Outcomes to Evaluate Effectiveness for Cardiac Care" (IMPROVE-Cardiac Care)R01HL161458 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MASTERSON CREBER, RUTH MARIE · 2022 to 2025
$2.6M
NHLBI NIH HHS R01 HL161458
6 · The paper itself

Abstract

Background: Patient-reported outcomes (PROs) capture where patients are on their disease trajectory and can identify changes in health status from their perspective. Objectives: This study applied the equity and sustainability-informed RE-AIM framework (Reach, Effectiveness, Adoption, Implementation, and Maintenance) to gain insights into clinical informatics interventions for collection and use of PROs across health systems. Methods: A total of 14 health informatics and clinical professionals were interviewed about the development and use of PROs within their health systems and individual practices. Directed content analysis was performed to highlight patterns, similarities, and differences in stakeholder perspectives across RE-AIM domains. Results: The reach of clinical informatics interventions using PROs varied across clinical practices and settings based upon institutional commitment and support, integration of clinical information systems, and engagement with patients and families. Although interventions using PROs were viewed as effective for enabling focused conversations with patients and facilitating shared decision-making, barriers to adoption included licensing requirements associated with PRO instruments, lack of incentives for their use, limited integration of PRO results into electronic medical record systems, and poor support for patients with low technology and/or health literacy. Implementation of interventions using PROs was facilitated through training and support staff who aided clinicians with clinical workflow integration, availability of questionnaires in multiple languages, identifying thresholds and strategies for action, and presenting interpretable visualizations showing changes over time alongside significant clinical events. Maintenance of interventions using PROs was enabled through multimodal data collection approaches and data governance groups that evaluated organizational requests to track new measures. Conclusion: Initiatives to increase the reach of clinical informatics interventions using PROs will require health system investments into medical record system integration, education, and implementation support for clinicians and patients, and efforts to reach patient populations with language barriers or limited technology literacy.

Indexed as

equitypatient-reported outcomesqualitativeRE-AIMsustainability

Identifiers

PMID40487468
PMCPMC12143486

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.