Evidence map›Paper›PMID 35275557›Full record

ArticleJournal of Parkinson's disease2022

Patient-Related Factors Influencing Caregiver Burden in Parkinson's Disease Patients: Comparison of Effects Before and After Deep Brain Stimulation.

Marle M Van Hienen, Roy Kuiper, Huub A M Middelkoop, Jacobus J Van Hilten, Maria Fiorella Contarino, Victor J Geraedts

Abstract read
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Article in Journal of Parkinson's disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Marle M Van HienenDepartment of Neurology, LUMC, Leiden, the Netherlands.
Roy KuiperDepartment of Neurology, LUMC, Leiden, the Netherlands.
Huub A M MiddelkoopDepartment of Neurology, LUMC, Leiden, the Netherlands.
Jacobus J Van HiltenDepartment of Neurology, LUMC, Leiden, the Netherlands.
Maria Fiorella ContarinoDepartment of Neurology, LUMC, Leiden, the Netherlands.
Victor J GeraedtsDepartment of Neurology, LUMC, Leiden, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCaregivers of Parkinson's disease (PD) patients provide important support during the pre- and postoperative phase of deep brain stimulation (DBS). High levels of caregiver burden have been reported after DBS. However, a comparison between preoperative and postoperative burden and associated factors has been insufficiently studied.

objectiveTo investigate the influence of DBS on caregiver burden, and to identify the differential impact of patient-related factors on caregiver burden before and after DBS.

methodsConsecutive patients referred for DBS eligibility screening or during one-year follow-up assessments were included. Caregiver burden was measured with the short Zarit Burden Interview (ZBI-12). Inverse Probability Weighting (IPW) was used to compare caregiver burden between preoperative and postoperative assessments.

resultsWe included 47 patients (24 screening, 23 follow-up) (median age 65 years, 29.4% female sex). DBS did not impact caregiver burden (screening: median ZBI-12 9.5 (IQR 3.25, 16.75); follow-up median ZBI-12 6 (IQR 4, 14); IPW-coefficient 0.57 (95% CI -2.75, 3.89)). Worse caregiver burden during DBS screening was associated with worse patient-related scores on depressive symptoms, anxiety, QoL, and impulsiveness. Worse scores on depressive symptoms, anxiety, apathy, postural-instability-gait-disorder, and QoL were associated with worse caregiver burden at one-year follow-up.

conclusionDBS appears not associated with changes in caregiver burden. Various symptoms are valued differently between screening and follow-up assessments in terms of caregiver burden. Early recognition of caregivers "at risk" may improve guidance of patient-caregiver dyads throughout the DBS process.

Indexed as

Deep Brain StimulationParkinson DiseaseAgedCaregiver BurdenCaregiversFemaleHumansMaleQuality of Lifecaregiver burdendeep brain stimulationepidemiologyParkinson’s diseasequality of life

Identifiers

PMID35275557
PMCPMC9484085

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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.