Evidence map›Paper›PMID 31185964›Full record

ArticleBMC medical education2019

Bridging the gap in genetics: a progressive model for primary to specialist care.

Brittany Harding, Colleen Webber, Lucia Rühland, Nancy Dalgarno, Christine Armour, Richard Birtwhistle, Glenn Brown, June C Carroll, Michael Flavin, Susan P Phillips and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical education, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
2.1field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 3 syntheses or guidelines pooled it, 38 citations in OpenAlex.

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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

11 authors at 4 institutions in 1 country.

Brittany HardingDepartment of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
Colleen WebberQueen's University, 99 University Avenue, Kingston, Ontario, K7L 3N6, Canada.
Lucia RühlandQueen's University, 99 University Avenue, Kingston, Ontario, K7L 3N6, Canada.
Nancy DalgarnoBotterell Hall, Queen's University, 18 Stuart Street, Kingston, Ontario, K7L 3N6, Canada.
Christine ArmourChildren's Hospital of Eastern Ontario, 401 Smyth Road, Ottawa, Ontario, K1H 8L1, Canada.
Richard BirtwhistleDepartment of Public Health, Kingston, Ontario, Canada.
Glenn BrownCentre for Studies in Primary Care, Queen's University, 220 Bagot Street, P.O.#8888, Kingston, Ontario, K7L 5E9, Canada.
June C CarrollDepartment of Family and Community Medicine, Granovsky Gluskin Family Medicine Centre, Mount Sinai Hospital, University of Toronto, 60 Murray St., 4th Floor, Box 25, Toronto, Ontario, M5T 3L9, Canada.
Michael FlavinDepartment of Pediatrics, Faculty of Health Sciences, Queen's University, Kingston, Ontario, Canada.
Susan P PhillipsCentre for Studies in Primary Care, Queen's University, 220 Bagot Street, P.O.#8888, Kingston, Ontario, K7L 5E9, Canada.
Jennifer J MacKenzieDepartment of Pediatrics, McMaster Children's Hospital, 1280, Main St. West, 3N11-G, Hamilton, Ontario, L8S 4K1, Canada. mackej4@mcmaster.ca.ORCID http://orcid.org/0000-0002-3374-8619
Queen's University · CAChildren's Hospital of Eastern Ontario · CAMcMaster University · CAMount Sinai Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe rapid expansion of genetic knowledge, and the implications for healthcare has resulted in an increased role for Primary Care Providers (PCPs) to incorporate genetics into their daily practice. The objective of this study was to explore the self-identified needs, including educational needs, of both urban and rural Primary Care Providers (PCPs) in order to provide genetic care to their patients.

methodsUsing a qualitative grounded theory approach, ten key informant interviews, and one urban and two rural PCP focus groups (FGs) (n = 19) were conducted. All PCPs practiced in Southeastern Ontario. Data was analyzed using a constant comparative method and thematic design. The data reported here represent a subset of a larger study.

resultsParticipants reported that PCPs have a responsibility to ensure patients receive genetic care. However, specific roles and responsibilities for that care were poorly defined. PCPs identified a need for further education and resources to enable them to provide care for individuals with genetic conditions. Based on the findings, a progressive stepped model that bridges primary and specialty genetic care was developed; the model ranged from PCPs identifying patients with genetic conditions that they could manage alone, to patients who they could manage with informal or electronic consultation to those who clearly required specialist referral.

conclusionsPCPs identified a need to integrate genetics into primary care practice but they perceived barriers including a lack of knowledge and confidence, access to timely formal and informal consultation and clearly defined roles for themselves and specialists. To address gaps in PCP confidence in providing genetic care, interventions that are directed at accessible just-in-time support and consultation have the potential to empower PCPs to manage patients' genetic conditions. Specific attention to content, timing, and accessibility of educational interventions is critical to address the needs of both urban and rural PCPs. A progressive framework for bridging primary to specialty care through a 'stepped' model for providing continuing medical education, and genetic care can was developed and can be used to guide future design and delivery of educational interventions and resources.

Indexed as

Genetics, MedicalNeeds AssessmentPhysicians, Primary CareAdultFemaleFocus GroupsGrounded TheoryHumansInterviews as TopicMaleMiddle AgedOntarioContinuing medical educationGenetic careGeneticsPreventionPrimary care providersUndergraduate medical education

Identifiers

PMID31185964
PMCPMC6558677
OpenAlexW2952729484

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.