Health-related quality-of-life and burden for caregivers of individuals with neurogenic orthostatic hypotension

Neurodegener Dis Manag. 2023 Feb;13(1):35-45. doi: 10.2217/nmt-2022-0015. Epub 2022 Nov 16.

Abstract

Aim: This study explores the burden of caring for an individual with neurogenic orthostatic hypotension (nOH) and an underlying neurodegenerative disease (Parkinson's disease, multiple system atrophy, pure autonomic failure or dementia with Lewy bodies). Materials & methods: A survey including several validated instruments was conducted with informal caregivers of individuals with Parkinson's disease, multiple system atrophy, pure autonomic failure or dementia with Lewy bodies. Results: Caregivers of patients with nOH (n = 60) reported greater burden across all outcomes compared with those without nOH (n = 60). Receiving pharmacological treatment for nOH was the variable most consistently associated with significantly better caregiver health-related quality-of-life (p < 0.05). Conclusion: This study demonstrates the burden of nOH on informal caregivers and highlights the potential benefit of pharmacological treatment not only for patients but also indirectly, their caregivers.

Keywords: Parkinson’s disease; caregiver burden; dementia with Lewy bodies; multiple system atrophy; neurogenic orthostatic hypotension; pure autonomic failure.

Plain language summary

Neurogenic orthostatic hypotension (nOH) causes blood pressure to fall when you stand up, meaning you can feel dizzy or lightheaded. This study looked at how providing day to day caregiving support to someone who has nOH as well as another neurological condition impacts the caregiver’s health and wellbeing. These neurological conditions included Parkinson’s disease, multiple system atrophy, pure autonomic failure or dementia with Lewy bodies. A survey was conducted with informal caregivers (e.g., family members) of people with a neurological condition, with or without nOH. Caregivers completed questions about their own health-related quality-of-life, anxiety, depression and experience of caregiving. Caregivers of patients with nOH reported higher amounts of burden compared with those without nOH. Patients taking a treatment for nOH was most often associated with better caregiver health-related quality-of-life. This study shows the burden nOH can have on informal caregivers and highlights that treatment potentially benefits both patients and, indirectly, caregivers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caregivers
  • Humans
  • Hypotension, Orthostatic* / complications
  • Hypotension, Orthostatic* / drug therapy
  • Lewy Body Disease* / drug therapy
  • Multiple System Atrophy*
  • Parkinson Disease* / complications
  • Pure Autonomic Failure* / complications
  • Quality of Life