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. 2014 Dec 1;14(19):1–72.

Table 3:

Description of Interventions and Outcomes

Author, Year Interventions Comparisons Outcomes of Interest
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
  • Concordance between patient wishes and care received

  • Concordance between patient's and surrogate's wishes

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
  • Informal caregiver's QoL

  • Carer and family's satisfaction with care

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
  • Patient's QoL

  • Patient's satisfaction with care

  • Completion of ACP documents and processes

  • Hospital LOS

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
  • Hospital LOS

  • ICU LOS

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
  • Family's satisfaction with care

  • Hospital care

  • Hospital LOS

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
  • Patient's QoL

  • Completion of ACP documents and processes

  • Hospital care

  • Emergency department visits

  • Home health visits

  • Outpatient services

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
  • Tool: none (assumed)

  • Type: single-provider (assumed)

  • Duration: NA

  • Frequency: NA

  • Topics: NA

No discussiona
  • Concordance between patient's wishes and care received

  • Hospice care

Wright et al, 2008 (60)a
  • Tool: none (assumed)

  • Type: single-provider (assumed)

  • Duration: NA

  • Frequency: NA

  • Topics: NA

No discussiona
  • Chemotherapy

  • Hospice care

Casarett et al, 2008 (61) Palliative care consultation
  • Tool: none

  • Type: team-based; physician, nurse practitioner, or both; social worker; nurse; chaplain; volunteers; and other professionals as needed

  • Duration: NA

  • Frequency: NA

  • Topics: NA

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
  • Tool: none (assumed)

  • Type: single-provider; physician

  • Duration: NA

  • Frequency: NA Topics: preferencesa

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
  • Completion of ACP documents and processes

  • Hospital LOS

  • ICU LOS

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
  • Hospital LOS

  • ICU LOS

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
  • Concordance between patient's wishes and care received

  • Completion of ACP documents and processes

Cross-sectional
Leung et al, 2012 (67)a
  • Tool: none (assumed)

  • Type: single-provider; physician

  • Duration: NA

  • Frequency: NA Topics: care planninga

No discussiona Patient's satisfaction with care
Mori et al, 2013 (68)a
  • Tool: none (assumed)

  • Type: single-provider; health care provider

  • Duration: NA

  • Frequency: NA

  • Topics: NA

No discussiona Family's satisfaction with care
Heyland et al, 2009 (11)a
  • Tool: none (assumed)

  • Type: single-provider; health care provider

  • Duration: NA

  • Frequency: NA

  • Topics: NA

No discussiona
  • Patient's satisfaction with care

  • Family's satisfaction with care

Abbreviations: ACP, advance care planning; AD, advance directive; CPR, cardiopulmonary resuscitation; EoL, end of life; ICU, intensive care unit; LOS, length of stay; NA, not available; QoL, quality of life; RCT, randomized controlled trial; STP, statement of treatment preferences; VALUE, value comments made by the family, acknowledge family emotions, listen, understand the patient as a person, elicit family questions.

a

Additional information was not provided.