Randomized controlled trials (RCTs) |
Kirchhoff et al, 2012; (40) Kirchhoff et al, 2010 (41) |
Tool: facilitation tool
Type: single-provider; nurse, social worker, or chaplain who was trained to deliver the intervention
Duration: 1.0–1.5 hours
Frequency: NA
Topics: patient and surrogate understanding, information about treatment, assistance with documentation of care preferences, surrogate understanding of patient preferences, preparing surrogate to make decisions that honour patient preferences; completion of STP
|
Usual care: standard AD counseling, assessment of AD on admission, question whether patient wanted more information, referrals according to institutional protocol |
|
Au et al, 2012 (42) |
Tool: automated form
Type: single-provider; physician
Duration: NA
Frequency: NA
Topics: barriers and facilitators to EoL communication, patient preferences
|
Usual carea
|
Completion of ACP documents and processes |
Sampson et al, 2011 (51) |
Tool: framework
Type: single-provider; nurse
Duration: NA
Frequency: up to 4 consultations at least 5 days apart
Topics: knowledge; illness severity and prognosis; patient's physical needs; social situation and social support; previous care preferences; cultural, spiritual, health, social, financial needs; role of palliative care; ACP
Other: included a needs assessment, discussion with carers and family, summary of discussion in a standard form
|
Usual carea
|
|
Detering et al, 2010 (39) |
Tool: Respecting Patient Choices model
Type: single-provider; nurse who was trained to deliver the intervention; a physician was sometimes included
Duration: Median length of discussion was 60 minutes (range 10–200 minutes)
Frequency: NA
Topics: prognosis, goals, values, beliefs, discuss and document choices for future health care, ACP
Other: offered on top of usual care
|
Usual care: no ACP unless specifically requested |
Patient's satisfaction with care
Informal caregiver's and family's satisfaction with care
Completion of ACP documents and processes
|
Gade et al, 2008 (43) |
Tool: Weismann's palliative care components
Type: team-based; physician, nurse, social worker, and chaplain
Duration: NA
Frequency: NA
Topics: symptom management, psychosocial and spiritual support, EoL planning, posthospital care, diagnosis, prognosis, goals of care, ACP
|
Usual carea
|
|
Clayton et al, 2007 (44) |
Tool: question prompt list with 112 potential questions that was reviewed 20–30 minutes before the consultation
Type: single-provider; physician
Duration: NA
Frequency: NA
Topics: palliative care, physical symptoms, treatment, lifestyle and QoL, prognosis, support, EoL issues
|
Usual care: routine consultation |
Patient's satisfaction with care |
Lautrette et al, 2007 (45) |
Tool: VALUE mnemonic, a brochure, and detailed procedures
Type: team-based; physician and other professionals
Duration: Median length of discussion was 30 minutes (range 19–45 minutes)
Frequency: NA
Topics: NA
|
Usual care: EoL family conference |
ICU LOS |
Gilmer et al, 2005 (46) |
Tool: process model
Type: team-based; ethicist consultant and other professionals
Duration: NA
Frequency: NA
Topics: ethical issues, hospital policy, ethical consensus statements, statutes, laws, measures to improve communication, medical factors, patient preferences and values, QoL, context
|
Usual care: no ethics consultation was offered |
|
Casarett et al, 2005 (48) |
Tool: structured interview questionnaire
Type: single-provider; physician
Duration: NA
Frequency: NA
Topics: goals of care, life-sustaining treatment, symptoms, palliative care needs (i.e., comfort care, nursing support, practical support, ACP, emotional support, bereavement support, spiritual support, address loneliness)
|
Usual care: assessment by research assistant |
|
Song et al, 2005 (49) |
Tool: Representational Approach model
Type: single-provider; nurse
Duration: NA
Frequency: NA
Topics: ACP, illness experiences, misconceptions and concerns, informed choices about medical care, treatment, complications, benefits
Other: offered in addition to usual care
|
Usual care: information cards and a booklet if more information was desired |
Concordance between patient's and surrogate's wishes |
Nicolasora et al, 2006 (47) |
Tools: script that provides detailed information about life-sustaining treatments and ADs
Type: single-provider; physician
Duration: NA
Frequency: NA
Topics: completion of ACP, CPR status, patient wishes for change, AD creation
|
Usual care: not approached by physician |
Completion of ACP documents and processes |
Dyar et al, 2012 (50) |
Tool: none
Type: single-provider; nurse practitioner
Duration: NA
Frequency: NA
Topics: Five Wishes (a living will), information about hospices, needs assessment
|
Usual carea
|
Patient's QoL |
Jones et al, 2011 (52) |
Tool: none
Type: single-provider; nurse or physician who was trained to deliver the intervention
Duration: NA
Frequency: NA
Topics: patient perceptions, communication with providers and family, hopes and fears for future, health care decision-making
Other: family members were not invited to the first consultation, but they were included in subsequent sessions
|
Usual carea
|
Patient's satisfaction with care |
Observational with contemporaneous controls |
Evangelista et al, 2012 (54) |
Tool: none
Type: single-provider; nurse or physician
Duration: 50–120 minutes
Frequency: NA
Topics: patient's values, goals, preferences; areas where patient perceived the need for support (e.g., physical, symptom control, emotional support, illness understanding, treatment goals, ACP); establish treatment plan
|
Usual care: no palliative care consultation |
Patient's QoL |
Jacobsen et al, 2011 (55) |
Tool: cognitive model for ACP
Type: single-provider; physician, nurse, or social worker
Duration: NA
Frequency: NA
Topics: information sharing ACP meetings, understanding, values, goals, preferences, selection of surrogate, prognosis, hopes, worries, CPR, place of death
|
Usual carea
|
Completion of ACP documents and processes |
Engelhardt et al, 2009 (56) |
Tool: checklist
Type: single-provider; social worker or health educator
Duration: NA
Frequency: took place over 6 sessions
Topics: understanding, treatment, symptoms, prognosis, communication with providers, ACP, coping, existential issues, caregiving concerns, long-term care planning, home environmental modifications, etc.
Other: in-person discussion followed by phone contact
|
Usual carea
|
|
Rabow et al, 2004 (57) |
Tool: none
Type: team-based; social worker, nurse, chaplain, pharmacist, psychologist, art therapist, volunteer coordinator, and 3 physicians
Duration: NA
Frequency: took place over 3 sessions
Topics: NA
Other: provided in addition to usual care
|
Usual carea
|
Patient's QoL
Patient's satisfaction with care
Completion of ACP documents and processes
Hospital care
Hospital LOS
Emergency department visits
Urgent care visits
Outpatient services
|
Mack et al, 2012 (58) |
Tool: none
Type: single-provider; 40% of discussions included a physician
Duration: NA
Frequency: NA
Topics: ACP (i.e., do not resuscitate, hospices, palliative care, or not otherwise specified), venue of dying
|
No discussiona
|
Chemotherapy
Hospital care
ICU admission
Hospice care
|
Mack et al, 2010 (59)a
|
|
No discussiona
|
|
Wright et al, 2008 (60)a
|
|
No discussiona
|
Chemotherapy
Hospice care
|
Casarett et al, 2008 (61) |
Palliative care consultation
|
Usual carea
|
Patient's QoL |
Morrison et al, 2005 (62) |
Tool: aid to structure discussions
Type: single-provider; social worker trained to deliver intervention
Duration: NA
Frequency: NA
Topics: patient's decisional capacity, information on how to appoint proxies, communication with proxies, ACP, goals of care, feedback to physicians on congruence
|
Usual carea
|
Concordance between patient's wishes and care received |
Zhang et al, 2009 (53)a
|
|
No discussiona
|
Patient's satisfaction
Chemotherapy
Resuscitation
ICU admission
Hospice care
|
Briggs et al, 2004 (63) |
Tool: aid to structure discussions
Type: single-provider; nurse, chaplain, or social worker who was trained to deliver the intervention
Duration: 1 hour
Frequency: NA
Topics: patient and surrogate understanding, information about treatment, assistance with ACP documentation, surrogate's understanding of patient's preferences, preparing surrogate to make decisions that honour patient preferences, complete STP
|
Usual care: ACP literature, referral to trained ACP facilitator |
Concordance between patient's and surrogate's wishes |
Observational with historical controls |
Lamba et al, 2012 (64) |
Tool: none
Type: team-based; Part I (physician and nurse), Part II (physician, nurse, counsellor, and interfaith pastor)
Duration: NA
Frequency: NA
Topics: Part I (prognosis, ADs, family support, surrogate decision-maker, pain, other symptoms), Part II (likely patient outcomes; treatment options; goals of care; assessment of content on goals of care discussion, family understanding, issues of conflict)
|
Usual carea
|
|
Norton et al, 2007 (65) |
Tool: none
Type: team-based; nurse practitioner, physician, chaplain, music therapist, massage therapist, and psychologist
Duration: NA
Frequency: NA
Topics: medical history and physical exam, palliative care, involvement with team and family, other providers
|
Usual care: physician makes a palliative care referral |
|
Lindner et al, 2007 (66) |
Tool: electronic medical record note
Type: single-provider; physician
Duration: NA
Frequency: NA
Topics: information about surrogates, dates and content of prior written ADs, values, preferences, goals of care, wishes regarding resuscitation, artificial nutrition, hydration, hospital transfer, autopsy
|
Usual carea
|
|
Cross-sectional |
Leung et al, 2012 (67)a
|
|
No discussiona
|
Patient's satisfaction with care |
Mori et al, 2013 (68)a
|
|
No discussiona
|
Family's satisfaction with care |
Heyland et al, 2009 (11)a
|
|
No discussiona
|
|