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. 2014 May 1;17(5):579–584. doi: 10.1089/jpm.2013.0551

Table 1.

Sample Description

  Study sample (n=71) Historical samplea (n=2043)
  N % %
Patient/Family Participants
 Age
  <60 years 23 32 36
  60 to <80 years 26 37 39
  ≥80 years 22 31 25
 Gender
  Women 33 46 47
  Men 38 54 53
 Reported race
  Black 5 7 14
  White 66 93 79
 Main diagnosis
  Cancer 35 49 46
  CHF/COPD 9 13 17
  CVA 7 10 6
  Other 20 28 30
 Patient/Family Verbal Participation
  Patient only 18 25 Unavailable
  Patient and family 24 34  
  Family only 29 41  
 Severe symptoms?
  Yes 29 41 37
  No 42 59 63
 Palliative Performance Score
  ≤30 30 42 46
  40–50 23 32 31
  ≥60 18 26 23
Composition of PC team
 Participating membersb
  Attending physician only 30 42 Unavailable
  Attending physician+NP/fellow 25 35  
  Attending physician, NP+fellow 16 23  
a

“Goals of care” or “end-of-life decision-making” consultations (January 2006 to January 2010), no statistically significant differences in comparisons to study sample characteristics.

b

Internal medical residents and medical students trainees were present for many conversations but did not contribute substantively.

CHF, congestive heart failure; COPD, chronic obstructive pulmonary disease; CVA, other; NP, nurse practioner; PC, palliative care.