Abstract

BackgroundWhile advance care planning (ACP) has been shown to improve the quality of end-of-life (EOL) communication and palliative care, it is rarely practiced in long term care (LTC) homes, where staff time to support the process is limited. This study examines the potential of a publicly available self-directed ACP workbook distributed to LTC residents to encourage ACP reflection and communication.MethodsRecruitment took place across three LTC homes, between June 2018 and July 2019. To be eligible, residents had to have medical stability, cognitive capacity, and English literacy. The study employed a mixed methods concurrent design using the combination of ranked (quantitative) and open (qualitative) workbook responses to examine documented care preferences and ACP reflections and communications.Results58 residents initially agreed to participate in the study of which 44 completed self-directed ACP workbooks. Our combined quantitative and qualitative results suggested that the workbooks supported the elicitation of a range of resident care preferences of relevance for EOL care planning and decision making. For example, ranked data highlighted that most residents want to remain involved in decisions pertaining to their care (70%), even though less than half expect their wishes to be applied without discretion (48%). Ranked data further revealed many residents value quality of life over quantity of life (55%) but a sizable minority are concerned they will not receive enough care at EOL (20%). Open comments affirmed and expanded on ranked data by capturing care preferences not explored in the ranked data such as preferences around spiritual care and post mortem planning. Analysis of all open comments also suggested that while the workbook elicited many reflections that could be readily communicated to family/friends or staff, evidence that conversations had occurred was less evident in recorded workbook responses.ConclusionsACP workbooks may be useful for supporting the elicitation of resident care preferences and concerns in LTC. Developing follow up protocols wherein residents are supported in communicating their workbook responses to families/friends and staff may be a critical next step in improving ACP engagement in LTC. Such protocols would require staff training and an organizational culture that empowers staff at all levels to engage in follow up conversations with residents.

Highlights

  • While advance care planning (ACP) has been shown to improve the quality of end-of-life (EOL) com‐ munication and palliative care, it is rarely practiced in long term care (LTC) homes, where staff time to support the process is limited

  • Legally appointed substitute decision-makers (SDMs) who have limited knowledge of their family member’s/friend’s preferences may feel burdened when making care decisions on their behalf [2]. These concerns are an urgent priority in long-term care (LTC), where many residents experience the deterioration of their cognitive capacity due to progressive, non-reversible health conditions [3]

  • The extent to which these self-directed tools can facilitate ACP engagement amongst LTC residents has yet to be explored. Addressing this important gap in the literature, our study examined the scope of future care preferences elicited by a self-directed ACP workbook, called Your Conversation Starter Kit, when distributed amongst residents in LTC

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Summary

Introduction

While advance care planning (ACP) has been shown to improve the quality of end-of-life (EOL) com‐ munication and palliative care, it is rarely practiced in long term care (LTC) homes, where staff time to support the process is limited. Legally appointed substitute decision-makers (SDMs) who have limited knowledge of their family member’s/friend’s preferences may feel burdened when making care decisions on their behalf [2]. These concerns are an urgent priority in long-term care (LTC), where many residents experience the deterioration of their cognitive capacity due to progressive, non-reversible health conditions [3]. ACP improves concordance between patients’ and family/friends’ preferred EOL wishes and family satisfaction with care while reducing family stress, anxiety, and depression [6, 7]

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