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Realities, Expectations and Attitudes to Life Support Technologies in Intensive Care for Octogenarians:

Completed
Conditions
Critically Ill
Registration Number
NCT01293708
Lead Sponsor
Daren K. Heyland
Brief Summary

The purpose of this study is to understand the realities, expectations and attitudes of patients 80+ and their families about the use of life-sustaining technology, and to document the patient outcomes and family experiences associated with surviving and not surviving critical illness. Specifically in this project the investigators will determine the real outcomes of critical illness experienced by octogenarians.

Detailed Description

Seriously ill hospitalized elderly patients rate 'not being kept alive on prolonged life supports' as the most important aspect of good quality care at the end of life (EOL). Across Canada, large numbers of elderly patients near the EOL and their families are faced with decisions about whether or not to use mechanical ventilation or other forms of life support technology used in intensive care units (ICUs). The investigators do not know whether these patients and their families are informed about the realities of intensive care - that is, if they are aware of the likelihood of surviving a critical illness and the resultant health states. The outcomes of critical illness for this patient population and their families are unknown, despite the crucial importance of this information to guide clinical decision making. The goals of our research program are to understand the realities of critical care, and the expectations and attitudes of patients 80 years of age or older (80+) and their families about the use of life sustaining technology. Specifically, in this project, the investigators want to determine the realities or outcomes of surviving critical illness.

Our primary research question is:

1. What are the 12-month health-related quality of life (HRQOL), functional status, and survival of patients admitted to ICU who are 80+ years old?

Our secondary research questions are:

2. Which patient characteristics are associated with 12-month HRQOL, functional status, and survival?

3. What is the satisfaction of family members with critical care, as measured by the Family Satisfaction in ICU (FS-ICU 24) instrument?

4. For patients surviving their ICU stay, what is the experience of family members caring for the patient during follow up, as measured by the Caregiver Reaction Assessment (CRA) instrument?

5. For patients who do not survive their ICU stay, what is the family satisfaction with EOL care, as measured using the CANHELP Satisfaction (Bereavement) instrument?

6. What is the health-related financial burden experienced by patients and their caregivers during their initial ICU hospitalization and up to 12 months after the index ICU admission?

7. What is the quality of decision making regarding the goals of care for an 80+ ICU patient?

8. What are the values that influence decisions about the goals of care for this population?

To answer these questions, the investigators are conducting a national, multicentre, cohort study of 800 patients age 80+ years who are admitted to Canadian ICUs. The investigators will follow these patients prospectively for 12 months to measure study outcomes. In addition, using novel instruments that the investigators have already developed and validated, the investigators will follow family members of these patients to document their experience as caregivers, their satisfaction with care of their relatives, and the financial implications of having a critically ill loved one. This quantitative project will be complemented by a separate qualitative study in the community setting to further understand the expectations and attitudes of persons over 80 years of age regarding the use of life sustaining technology. Data emerging from this work will inform important clinical decisions regarding critical care and EOL care for this aged population.

The investigators presume that the short- and long-term mortality of 80+ year olds admitted to Canadian ICUs will be high and that the self-reported health-related quality of life and functional status of survivors after hospital discharge will be low. The investigators anticipate that pre-morbid illnesses and functional status before admission to ICU will correlate with long-term clinical outcomes. The investigators are uncertain as to the psychological and financial burden experienced by families when a loved one is in the ICU and during the recovery phase; our study will be the first to furnish such important information. By using administrative databases to complement information already being collected in this study, the investigators will obtain a better understanding of the healthcare resource utilization and longer term survival of this cohort, and will be better positioned to offer effective ICU and follow-up care for this at-risk patient population.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1504
Inclusion Criteria
  • minimum stay in the ICU of 24 hrs
  • patient is >=80 years old
  • patient is a resident of Canada and has a permanent address in this country
  • patient has an eligible family caregiver who has visited the patient at least once within 96 hours of the current ICU admission
Exclusion Criteria
  • family caregiver is <= 18
  • family caregiver is paid to do so
  • family caregivers that do not speak English or French
  • previously enrolled

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Health Related Quality of Life (HRQOL)12 months

To determine the 12 month HRQOL of 80+ year olds admitted to the ICU in Canada.

Secondary Outcome Measures
NameTimeMethod
To determine which patient characteristics are associated with survival12 months
To determine which patient characteristics are associated with 12-month HRQOL12 month
To determine which patient characteristics are associated with functional status.12 months

Trial Locations

Locations (24)

Toronto General Hospital

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Toronto, Ontario, Canada

Victoria General Hospital

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Vancouver, British Columbia, Canada

Royal Alexandra Hospital

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Edmonton, Alberta, Canada

Surrey Memorial Hospital

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Surrey, British Columbia, Canada

Grey Nuns Community Hospital

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Edmonton, Alberta, Canada

Hospital Maisonneuve-Rosemont

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Montreal, Quebec, Canada

Hospital de Sacre-Coeur

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Montreal, Quebec, Canada

St.Paul's Hospital

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Vancouver, British Columbia, Canada

Royal Columbian Hospital

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New Westminster, British Columbia, Canada

Royal Jubilee Hospital

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Vancouver, British Columbia, Canada

St. Michaels Hospital

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Toronto, Ontario, Canada

St. Joseph's Healthcare

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Hamilton, Ontario, Canada

Mount Sinai

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Toronto, Ontario, Canada

Departement d'Anesthesie

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Quebec, Canada

University of Alberta Hospital

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Calgary, Alberta, Canada

St. Boniface Hospital

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Winnipeg, Manitoba, Canada

Peter Lougheed Hospital

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Calgary, Alberta, Canada

Hospital Laval

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Quebec, Canada

Winnipeg Health Sciences Center

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Winnipeg, Manitoba, Canada

Kingston General Hospital

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Kingston, Ontario, Canada

Ottawa Hospital

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Ottawa, Ontario, Canada

Foothills Hospital

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Calgary, Alberta, Canada

Royal University Hospital

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Saskatoon, Saskatchewan, Canada

Sunnybrook Health Sciences

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Toronto, Ontario, Canada

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