Informing Decisions in Chronic Critical Illness: A Randomized Control Trial (RCT)

Overview

The purpose of this study is to test a communication intervention to support family decision-making for patients with chronic critical illness.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Supportive Care
    • Masking: Single (Outcomes Assessor)
  • Study Primary Completion Date: October 2014

Detailed Description

Increasing use of intensive care therapies by an aging population has created a new medical syndrome – "chronic critical illness" – encompassing multi-system derangements, recurrent complications, and protracted/permanent dependence on mechanical ventilation and other life-supports. Numbering >100,000 at any point in time, the chronically critically ill are a growing population of older adults and a serious national health problem. Annual expenditures for these patients are estimated at $24 billion, mostly for patients ≥ 65 years old. Yet 6-month mortality rates exceed those for most malignancies, impairments are severe among survivors, and return to the community is rare. Descriptive research has identified domains of information that are important for decision-making by patients/families about continuation of treatment in the chronic phase of critical illness, but has also revealed that decisions are often made without this information or patient goals of care as a context. In acute critical illness, scheduled, structured meetings and printed informational aids are effective for Intensive Care Unit (ICU) families, but no study has tested an intervention to inform and support decision-making about chronic critical illness. This study is a randomized, controlled, multi-center clinical trial of such an intervention. Specific Aims are: (1) To evaluate the impact on family- and patient-focused outcomes of a proactive program of protocolized, interdisciplinary, informational support meetings led by a palliative care physician, plus a printed informational aid, for families of chronically critically ill patients; and (2) To evaluate the impact of this intervention on utilization of critical care resources for the chronically critically ill. We hypothesize that as compared to usual care plus the printed aid, this intervention will effectively inform decision-making, improve family well-being, promote discussion of preferences for patient goals of care, and optimize critical care resource utilization, without increasing patient mortality.

Interventions

  • Behavioral: Supportive Information Team Group
    • A minimum of two protocolized, interdisciplinary, informational support meetings led by palliative care clinicians will be arranged with family members or other patient surrogates who participate in decision-making for individual chronically critically ill patients.

Arms, Groups and Cohorts

  • Experimental: Supportive Information Team Group
    • Protocolized information and support meetings led by palliative care clinicians
  • No Intervention: Usual Care Group

Clinical Trial Outcome Measures

Primary Measures

  • Hospital Anxiety and Depression Scale
    • Time Frame: Day 90

Secondary Measures

  • Hospital Anxiety and Depression Scale
    • Time Frame: Day 18-20
  • Impact of Events Scale-Revised
    • Time Frame: Day 90
  • Discussion of Preferences for Patients Goals of Care
    • Time Frame: Day 18-20
    • Subscale of Center for Gerontology and Health Care Research Toolkit
  • Quality of Communication
    • Time Frame: Day 18-20
    • Curtis Measure
  • Family Satisfaction in the Intensive Care Unit (ICU) Survey
    • Time Frame: Day 90
  • Modified Center for Gerontology and Health Care Research (CHCR) Tool
    • Time Frame: Day 90
  • Limitation of Intensive Care Unit (ICU) Therapy
    • Time Frame: Average of 60 days
    • Percent of patients with mechanical ventilation, renal replacement, vasopressors, or artificial nutrition withheld or withdrawn
  • Hospital Length of Stay
    • Time Frame: Average of 60 days
    • Days since randomization
  • Mortality
    • Time Frame: Day 90
  • Physician-Surrogate Discordance Score
    • Time Frame: day 18-20
  • Discussion of Preferences for Patients Goals of Care
    • Time Frame: Day 90
    • Subscale of Center for Gerontology and Health Care Research Toolkit

Participating in This Clinical Trial

Inclusion Criteria

  • Mechanically ventilated ≥ 7 days – Mechanically ventilated without > 96 hour interruption – Age ≥ 21 years – ICU MD does not expect patient will die within 72 hours – ICU MD does not expect patient will be liberated from the ventilator within 72 hours. Exclusion Criteria:

  • Previous admission to study ICU this hospitalization Mechanically ventilated at outside hospital for > 7 days before transfer – Chronic Neuromuscular (NM) Disease – Trauma – Burn – Previous palliative care consultation in this hospitalization – No family or other surrogate decision-maker – Family not available – Surrogate lacks English proficiency – Physician refused permission for research staff to approach the family

Gender Eligibility: All

Minimum Age: 21 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Icahn School of Medicine at Mount Sinai
  • Collaborator
    • National Institute of Nursing Research (NINR)
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Judith Nelson, MD, JD, Principal Investigator, Icahn School of Medicine at Mount Sinai
    • Shannon Carson, MD, Principal Investigator, University of North Carolina, Chapel Hill

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