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Hsien Seow

Biographic Data

ID5535987
NAMEHsien Seow
GIVEN NAMESHsien
FAMILY NAMESeow
SIGNATURESEOW H
AFFILIATIONSMcMaster University
ORCID0000-0001-6701-1714
VERIFIEDYes
TOTAL WORKS8
TOTAL CITATIONS1
WORKS AS AUTHOR8
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2010
LATEST PUBLICATION YEAR2026
H-INDEX1
  • Family Caregivers’ Perspectives on Direct Financial Support Programs

    Open Access•Midori Matthew, Michel Grignon et al.•ARTICLE•Canadian Journal on Aging / La…•2026

    Background and Objective This study examines how intensive caregivers in Nova Scotia who receive the provincial government’s Caregiver Benefit interpret and experience the program, particularly in the context of its ambiguous goals. Methods A qualitative descriptive methodological design was used to ensure that the reporting of findings remained close to participants’ own words and to emphasize the practicality of findings. Twenty family caregive…

  • Supporting the Journey Home

    Open Access•Hsien Seow, Joanna Vautour et al.•ARTICLE•International Journal of…•2024

    In Ontario, Canada, several training programs have been created to improve home-based palliative care in First Nations communities, though they primarily focus on meeting needs at end-of-life. Therefore, education focused on incorporating an early palliative care approach for community health-related workers is necessary. To address this gap, we tested the CAPACITI curriculum with 12 health care providers working in First Nations communities acro…

  • The impact of the Caremongering social media movement

    Open Access•Valerie Bishop, Daryl Bainbridge et al.•ARTICLE•Health & Social Care in the…•2022•References: 3

    Public health responses to the COVID-19 pandemic, such as business restrictions, social distancing and lockdowns, had social and economic impacts on individuals and communities. Caremongering Facebook groups spread across Canada to support vulnerable individuals by providing a forum for sharing information and offering assistance. We sought to understand the specific impacts of Caremongering groups on individuals 1 year after the pandemic began. …

  • Cost-effectiveness of Investment in End-of-Life Home Care to Enable Death in Community Settings

    Sarina R Isenberg, Peter Tanuseputro et al.•ARTICLE•Medical Care•2020•References: 31

    BACKGROUND: Many people with terminal illness prefer to die in home-like settings-including care homes, hospices, or palliative care units-rather than an acute care hospital. Home-based palliative care services can increase the likelihood of death in a community setting, but the provision of these services may increase costs relative to usual care. OBJECTIVE: The aim of this study was to estimate the incremental cost per community death for perso…

  • Predictors of caregiver burden across the home-based palliative care trajectory in Ontario, Canada

    Open Access•Denise N Guerriere, Denise Guerriere et al.•ARTICLE•Health & Social Care in the…•2015•Cited by: 1•References: 4

    Family caregivers of patients enrolled in home-based palliative care programmes provide unpaid care and assistance with daily activities to terminally ill family members. Caregivers often experience caregiver burden, which is an important predictor of anxiety and depression that can extend into bereavement. We conducted a longitudinal, prospective cohort study to comprehensively assess modifiable and non-modifiable patient and caregiver factors t…

  • Identifying changes in scores on the EORTC-QLQ-C30 representing a change in patients’ supportive care needs

    Open Access•Claire Snyder, Claire F Snyder et al.•ARTICLE•Quality of Life Research•2014

  • Dimensionality, Reliability and Validity of the InterRAI Depression Rating Scale in a Canadian Palliative Care Population

    Open Access•Kathryn Fisher, K A Fisher et al.•ARTICLE•Social Indicators Research•2014•References: 1

  • Using More End-of-Life Homecare Services is Associated With Using Fewer Acute Care Services

    Hsien Seow, Lisa Barbera et al.•ARTICLE•Medical Care•2010•References: 41

    BACKGROUND: Healthcare systems are investing in end-of-life homecare to reduce acute care use. However, little evidence exists on the timing and amount of homecare services necessary to reduce acute care utilization. OBJECTIVES: To investigate whether admission time to homecare and the amount of services, as measured by average nursing and personal support and homemaking (PSH) hours/week (h/wk), are associated with using acute care services at en…

  • Predictors of caregiver burden across the home-based palliative care trajectory in Ontario, Canada

    Open Access•Denise N Guerriere, Denise Guerriere et al.•ARTICLE•Health & Social Care in the…•2015•Cited by: 1•References: 4

    Family caregivers of patients enrolled in home-based palliative care programmes provide unpaid care and assistance with daily activities to terminally ill family members. Caregivers often experience caregiver burden, which is an important predictor of anxiety and depression that can extend into bereavement. We conducted a longitudinal, prospective cohort study to comprehensively assess modifiable and non-modifiable patient and caregiver factors t…

  • Using More End-of-Life Homecare Services is Associated With Using Fewer Acute Care Services

    Hsien Seow, Lisa Barbera et al.•ARTICLE•Medical Care•2010•References: 41

    BACKGROUND: Healthcare systems are investing in end-of-life homecare to reduce acute care use. However, little evidence exists on the timing and amount of homecare services necessary to reduce acute care utilization. OBJECTIVES: To investigate whether admission time to homecare and the amount of services, as measured by average nursing and personal support and homemaking (PSH) hours/week (h/wk), are associated with using acute care services at en…

  • Identifying changes in scores on the EORTC-QLQ-C30 representing a change in patients’ supportive care needs

    Open Access•Claire Snyder, Claire F Snyder et al.•ARTICLE•Quality of Life Research•2014

  • Dimensionality, Reliability and Validity of the InterRAI Depression Rating Scale in a Canadian Palliative Care Population

    Open Access•Kathryn Fisher, K A Fisher et al.•ARTICLE•Social Indicators Research•2014•References: 1

  • Predictors of caregiver burden across the home-based palliative care trajectory in Ontario, Canada

    Open Access•Denise N Guerriere, Denise Guerriere et al.•ARTICLE•Health & Social Care in the…•2015•Cited by: 1•References: 4

    Family caregivers of patients enrolled in home-based palliative care programmes provide unpaid care and assistance with daily activities to terminally ill family members. Caregivers often experience caregiver burden, which is an important predictor of anxiety and depression that can extend into bereavement. We conducted a longitudinal, prospective cohort study to comprehensively assess modifiable and non-modifiable patient and caregiver factors t…

  • Cost-effectiveness of Investment in End-of-Life Home Care to Enable Death in Community Settings

    Sarina R Isenberg, Peter Tanuseputro et al.•ARTICLE•Medical Care•2020•References: 31

    BACKGROUND: Many people with terminal illness prefer to die in home-like settings-including care homes, hospices, or palliative care units-rather than an acute care hospital. Home-based palliative care services can increase the likelihood of death in a community setting, but the provision of these services may increase costs relative to usual care. OBJECTIVE: The aim of this study was to estimate the incremental cost per community death for perso…

  • The impact of the Caremongering social media movement

    Open Access•Valerie Bishop, Daryl Bainbridge et al.•ARTICLE•Health & Social Care in the…•2022•References: 3

    Public health responses to the COVID-19 pandemic, such as business restrictions, social distancing and lockdowns, had social and economic impacts on individuals and communities. Caremongering Facebook groups spread across Canada to support vulnerable individuals by providing a forum for sharing information and offering assistance. We sought to understand the specific impacts of Caremongering groups on individuals 1 year after the pandemic began. …

  • Supporting the Journey Home

    Open Access•Hsien Seow, Joanna Vautour et al.•ARTICLE•International Journal of…•2024

    In Ontario, Canada, several training programs have been created to improve home-based palliative care in First Nations communities, though they primarily focus on meeting needs at end-of-life. Therefore, education focused on incorporating an early palliative care approach for community health-related workers is necessary. To address this gap, we tested the CAPACITI curriculum with 12 health care providers working in First Nations communities acro…

  • Family Caregivers’ Perspectives on Direct Financial Support Programs

    Open Access•Midori Matthew, Michel Grignon et al.•ARTICLE•Canadian Journal on Aging / La…•2026

    Background and Objective This study examines how intensive caregivers in Nova Scotia who receive the provincial government’s Caregiver Benefit interpret and experience the program, particularly in the context of its ambiguous goals. Methods A qualitative descriptive methodological design was used to ensure that the reporting of findings remained close to participants’ own words and to emphasize the practicality of findings. Twenty family caregive…

Medicine (7 works) · Nursing (6 works) · Palliative care (5 works) · Palliative Care and End-of-Life Issues (4 works) · Gerontology (3 works) · Political science (3 works) · Psychology (3 works) · Cancer survivorship and care (2 works) · Computer Science (2 works) · End-of-life care (2 works)

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