Literature DB >> 34147576

Palliative Care Intervention Trials for Adults Living With Progressive Central Nervous System Diseases and Their Caregivers: A Systematic Review.

HeatherE Leeper1, Diane Cooper2, TerriS Armstrong2.   

Abstract

CONTEXT: Interest in implementing palliative care for adults living with progressive central nervous system diseases (PCNSD) and their caregivers is increasing.
OBJECTIVES: To inform evidence-based practice and future research by critically evaluating randomized clinical trials (RCTs) investigating palliative care interventions (PCIs) for adults living with PCNSD and their caregivers using self-reported outcomes and the patient- and caregiver-reported outcome measures employed.
METHODS: A systematic search using PRISMA methods of EMBASE, PubMed, Scopus, Web of Science databases using index and keyword methods for articles published from inception through February 28, 2021 was performed. RCTs investigating PCI as their primary aim using patient- and/or caregiver-reported outcomes to assess PCI effectiveness in adults living with PCNSD and their caregivers were included for qualitative synthesis.
RESULTS: Five RCTs met criteria and used 21 unique outcome measures. Pooled patient diagnoses included multiple sclerosis, motor neuron disease and movement disorders, primarily Parkinson's Disease. All five RCTs assessed PCI effectiveness on patient symptom burden and caregiver burden, and three RCTs used patient QOL as a primary outcome. Overall risk of bias was low. Pooled positive findings were limited to very modest changes in patient QOL, specific physical symptoms and caregiver burden. Most outcome measures lacked clinimetric responsiveness to detect change whether caused by disease or an intervention to the patient or caregiver.
CONCLUSION: Sparse, low-certainty evidence for PCI impact on patient QOL, symptom burden and caregiver burden indicate future research should consider refining study populations, interventions, outcomes assessed and outcome measures to detect any change due to PCI. Published by Elsevier Inc.

Entities:  

Keywords:  Neurologic disease; caregiver-reported outcomes; neuro-palliative care; palliative care; palliative medicine; patient-reported outcomes; systematic review

Mesh:

Year:  2021        PMID: 34147576      PMCID: PMC8683574          DOI: 10.1016/j.jpainsymman.2021.06.010

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  78 in total

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4.  Determining minimally important differences for the PDQ-39 Parkinson's disease questionnaire.

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Journal:  Age Ageing       Date:  2001-07       Impact factor: 10.668

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Authors:  Heidrun Golla; Stephanie Mammeas; Maren Galushko; Holger Pfaff; Raymond Voltz
Journal:  Palliat Support Care       Date:  2015-06-17

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Journal:  Mov Disord       Date:  2007-05-15       Impact factor: 10.338

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8.  Impact of special care unit for patients with advanced Alzheimer's disease on patients' discomfort and costs.

Authors:  L Volicer; A Collard; A Hurley; C Bishop; D Kern; S Karon
Journal:  J Am Geriatr Soc       Date:  1994-06       Impact factor: 5.562

9.  Ethical challenges of outcome measurement in palliative care clinical practice: a systematic review of systematic reviews.

Authors:  Sandra Martins Pereira; Pablo Hernández-Marrero
Journal:  Ann Palliat Med       Date:  2018-07-11

10.  Effect of Short-term Integrated Palliative Care on Patient-Reported Outcomes Among Patients Severely Affected With Long-term Neurological Conditions: A Randomized Clinical Trial.

Authors:  Wei Gao; Rebecca Wilson; Nilay Hepgul; Deokhee Yi; Catherine Evans; Sabrina Bajwah; Vincent Crosby; Andrew Wilcock; Fiona Lindsay; Anthony Byrne; Carolyn Young; Karen Groves; Clare Smith; Rachel Burman; K Ray Chaudhuri; Eli Silber; Irene J Higginson
Journal:  JAMA Netw Open       Date:  2020-08-03
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