Evidence map›Paper›PMID 39502560›Full record

ArticleFrontiers in pediatrics2024

Key data elements for a successful pediatric rheumatology virtual visit: a survey within the PR-COIN network.

Y Ingrid Goh, Meghan E Ryan, Shoghik Akoghlanian, Rajdeep Pooni, Julia G Harris, Danielle R Bullock, Sheetal S Vora, Tzielan C Lee, Shirley M L Tse, Fatima Barbar-Smiley

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2024. 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

10 authors.

Y Ingrid GohDivision of Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada.
Meghan E RyanDivision of Rheumatology, Allergy & Immunology, Department of Pediatrics, University of Minneapolis, Minneapolis, MN, United States.
Shoghik AkoghlanianDepartment of Rheumatology, Nationwide Children's Hospital, Columbus, OH, United States.
Rajdeep PooniDivision of Pediatric Rheumatology, Department of Pediatrics, Stanford Medicine Children's Health, Palo Alto, CA, United States.
Julia G HarrisDivision of Rheumatology, Department of Pediatrics, Children's Mercy Kansas City, Kansas City, Missouri, United States.
Danielle R BullockUniversity of Minnesota Medical School, University of Minnesota, Minneapolis, MN, United States.
Sheetal S VoraDepartment of Pediatrics, Atrium Health Levine Children's, Charlotte, NC, United States.
Tzielan C LeeDivision of Pediatric Rheumatology, Department of Pediatrics, Stanford Medicine Children's Health, Palo Alto, CA, United States.
Shirley M L TseDivision of Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada.
Fatima Barbar-SmileyDepartment of Rheumatology, Nationwide Children's Hospital, Columbus, OH, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Juvenile idiopathic arthritis (JIA) is the most common childhood rheumatic disease which is commonly monitored by a combination of history, physical examination, bloodwork, and imaging. The COVID-19 pandemic prompted a rapid shift to telemedicine to ensure that patients continued to receive healthcare. The shift to telemedicine changed the methodology and ability of healthcare providers to monitor their patients' progress, as they were unable to perform direct hands-on assessments. The following survey sought to understand the impact of switching pediatric rheumatology healthcare delivery from in-person to telemedicine modality. Specifically, it sought to examine the rate of collection of critical data elements (CDE) for monitoring JIA disease activity and outcomes, barriers and facilitators to its collection, opinions on difficulty and importance of collecting CDE over telemedicine, tools and electronic medical record modifications that facilitated CDE collection, and other data elements that were important to collect during telemedicine visits. Methods: A cross-sectional survey was sent to healthcare providers at all PR-COIN centers who saw patients using telemedicine. Qualitative data was analyzed using descriptive statistics and qualitative data was analyzed using an inductive approach. Results: Survey respondents reported that they documented the CDE at least 75% of the time. Barriers to assessing and documenting critical data elements included (1) the inability to palpate or visualize all joints over telemedicine, (2) connectivity issues, and (3) forgetfulness with collecting all CDE. Respondents suggested using reminders within the electronic medical record to prompt documentation completeness and improve reliability. They also suggested including medication adherence, quality of life, and patient/caregiver satisfaction with their telemedicine experience as part of their documentation. A few centers reported that they had established processes to assist with data collection in advance of the telemedicine visit; however, the variation in responses reflects the need to standardize the process of providing care over telemedicine. Discussion: Multiple barriers and facilitators to collecting CDE during telemedicine visits exist. Given that a proportion of the population will continue to be seen over telemedicine, teams need to adapt their practices to consistently provide high-quality care over virtual platforms, ensuring that patients at any institution receive a standardized level of service.

Indexed as

data documentationeHealthpediatric rheumatologyquality of caretelehealthtelemedicinetelerheumatologyvirtual

Identifiers

PMID39502560
PMCPMC11535877

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.