PARTNER II: Improving Patient and Family Centered Care in Advanced Critical Illness
Anxiety, Depression
About this trial
This is an interventional supportive care trial for Anxiety focused on measuring decision making for incapacitated patients, intensive care, surrogate decision making, patient centered care, palliative care
Eligibility Criteria
Inclusion Criteria:
- 18 years of age or older
- Surrogate decision maker for ICU patient in one of 5 UPMC ICU's
Exclusion Criteria:
- Non-English Speaking
- Surrogate's loved one is for organ transplantation
- Not physically able to participate in family meeting
Sites / Locations
- UPMC Hamot
- UPMC Presby/Shady
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control
Behavioral: The PARTNER II Intervention
The control group will receive usual care, in which the frequency and content of physician-family communication is determined by the clinical team according to their usual practice. No study ICU has a protocolized approach to family communication and instead clinicians determine the timing and frequency of communication with families. All sites have palliative care services.
The PARTNER intervention is a multifaceted intervention delivered by a trained "PARTNER Champion" who has undergone 16 hours of intense communication training, with audit and feedback, quarterly booster training, and expert implementation support. Additionally, there is academic detailing of ICU physicians and ICU bedside nurses to augment the intervention. The PARTNER Intervention deploys three strategies to improve: 1) the timeliness and frequency of clinician-family communication, 2) the emotional and decision support provided to families and 3) the appropriate involvement of palliative care specialists.