Informing Decisions in Chronic Critical Illness: A Randomized Control Trial (RCT)
- Conditions
- Chronic Critical IllnessProlonged Mechanical Ventilation
- Interventions
- Behavioral: Supportive Information Team Group
- Registration Number
- NCT01230099
- Lead Sponsor
- Icahn School of Medicine at Mount Sinai
- Brief Summary
The purpose of this study is to test a communication intervention to support family decision-making for patients with chronic critical illness.
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 622
- 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.
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Supportive Information Team Group Supportive Information Team Group Protocolized information and support meetings led by palliative care clinicians
- Primary Outcome Measures
Name Time Method Hospital Anxiety and Depression Scale Day 90
- Secondary Outcome Measures
Name Time Method Hospital Length of Stay Average of 60 days Days since randomization
Mortality Day 90 Discussion of Preferences for Patients Goals of Care Day 90 Subscale of Center for Gerontology and Health Care Research Toolkit
Hospital Anxiety and Depression Scale Day 18-20 Limitation of Intensive Care Unit (ICU) Therapy Average of 60 days Percent of patients with mechanical ventilation, renal replacement, vasopressors, or artificial nutrition withheld or withdrawn
Quality of Communication Day 18-20 Curtis Measure
Family Satisfaction in the Intensive Care Unit (ICU) Survey Day 90 Modified Center for Gerontology and Health Care Research (CHCR) Tool Day 90 Impact of Events Scale-Revised Day 90 Physician-Surrogate Discordance Score day 18-20
Trial Locations
- Locations (4)
University of North Carolina School of Medicine
🇺🇸Chapel Hill, North Carolina, United States
Durham Regional Medical Center
🇺🇸Durham, North Carolina, United States
Duke University School of Medicine
🇺🇸Durham, North Carolina, United States
Icahn School of Medicine at Mount Sinai
🇺🇸New York, New York, United States