Evidence map›Paper›PMID 33843516›Full record

ArticleThe Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques2022

Effects of the COVID-19 Pandemic on Parkinson's Disease: a Single-Centered Qualitative Study.

Beatrice Ana-Maria Anghelescu, Veronica Bruno, Davide Martino, Pamela Roach

Open access · hybridAbstract read
In one paragraph

Article in The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 9% 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

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

4 authors at 1 institution in 1 country.

Beatrice Ana-Maria AnghelescuDepartment of Clinical Neurosciences, University of Calgary, Calgary, Canada.ORCID 0000-0002-5244-7635
Veronica BrunoDepartment of Clinical Neurosciences, University of Calgary, Calgary, Canada.
Davide MartinoDepartment of Clinical Neurosciences, University of Calgary, Calgary, Canada.
Pamela RoachHotchkiss Brain Institute, University of Calgary, Calgary, Canada.ORCID 0000-0001-7694-9309
University of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe public health measure restrictions across the world due to COVID-19 have inadvertently impacted the routines for people with Parkinson's disease (PD) and their care partners not only in terms of compromised neurological clinical care but also drastically changing the way of life to minimize the risk of becoming infected. This study explores initial PD patients' lived experiences to observe how quality of life and health care has been affected at the start of the COVID-19 pandemic and provide insight into the importance of patient engagement and virtual care.

methodsTwenty-two virtual, in-depth semi-structured interviews with persons diagnosed with PD who usually attend a Movement Disorders specialty clinic in Calgary, Alberta, were completed between April 28 and May 13, 2020, and the care partners that wished to participate. Interviews were recorded and transcribed, after which transcripts were analyzed and coded into relevant themes using NVivo 12.

resultsImpacts from the public health measures and COVID-19 results into three main themes: (1) Impacts of COVID-19 on PD Clinical Care; (2) Activities of Daily Living; (3) Attitudes and Perceptions. Participants reported worsening in motor and nonmotor symptoms and had to accommodate to clinical care via virtual means which were associated with limitations and suggestions for improvement of remote care.

conclusionThis study provides a unique opportunity for researchers to better understand the lived experiences of PD patients in all aspects of their life suggesting that innovative means are needed for facilitating virtual health care medicine and increased social interaction.

Indexed as

COVID-19Parkinson DiseaseActivities of Daily LivingAttitude to HealthHumansPandemicsQualitative ResearchQuality of LifeTelemedicineCOVID-19PandemicParkinson’s diseaseQualitativeQuality of careQuality of life

Identifiers

PMID33843516
PMCPMC8160494
OpenAlexW3152615247

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.