Evidence map›Paper›PMID 35464100›Full record

ArticleHealth and technology2022

Rapid implementation of telegenetic services during the COVID-19 pandemic allowed continuing patient access, but not equally for all.

Ryan Noss, Katherine Carlotti, Deanna Leingang, David Flannery

Abstract read
In one paragraph

Article in Health and technology, 2022. 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. Assessing genetic counseling efficiency with natural language processing.Journal of the American Medical Informatics Association : JAMIA · 2026
    Article
  2. 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

4 authors.

Ryan NossCenter for Personalized Genetic Health Care, Genomic Medicine Institute and Cleveland Clinic Community Care, Cleveland Clinic, Cleveland, OH USA.
Katherine CarlottiCenter for Personalized Genetic Health Care, Genomic Medicine Institute and Cleveland Clinic Community Care, Cleveland Clinic, Cleveland, OH USA.
Deanna LeingangCenter for Personalized Genetic Health Care, Genomic Medicine Institute and Cleveland Clinic Community Care, Cleveland Clinic, Cleveland, OH USA.
David FlanneryCenter for Personalized Genetic Health Care, Genomic Medicine Institute and Cleveland Clinic Community Care, Cleveland Clinic, Cleveland, OH USA.ORCID 0000-0002-3383-7275

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telegenetics is the use of telemedicine to deliver clinical genetic services to patients. During the COVID-19 public health emergency (PHE), telegenetics was essential for the Center of Personalized Genetic Healthcare (CPGH). This study reviews and analyzes in the context of the RE-AIM framework CPGH's rapid implementation of telegenetics and its impact. We conducted a chart review of all out-patient telegenetics encounters scheduled in CPGH during the first five weeks of the COVID-19 PHE. Data analyzed included demographics; number of encounters scheduled; subspecialties and providers; outcome of encounter (completed, cancelled, no- show); and telehealth platform used. Data were compared to data for out-patient encounters in 2019. In the first five weeks of the COVID-19 PHE, 465 virtual visits were scheduled and 428 were completed, involving all six subspecialties and 86% of CPGH providers. The no-show plus cancellation rate was significantly lower than in 2019. By week four, CPGH's virtual visit volume was 82% of its out-patient volume during the same time period in 2019. Patients over 60 and Black patients were significantly more likely to use phone-audio only appointments. CPGH rapidly implemented telegenetic services to continue providing care to patients. We identified success factors that enabled this. However, our analysis also identified a possible "digital divide" for Black and older patients.

Indexed as

Digital DivideGenetic servicesHealthcare policyTelegeneticsTelehealth

Identifiers

PMID35464100
PMCPMC9013520

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.