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. 2013 Oct;16(10):1227–1231. doi: 10.1089/jpm.2013.0040

Table 2.

The Impact of Palliative Care on Patient Quality of Life

Variables Estimate P value Estimate P value
Intercept 0.20 <0.0001 0.20 <0.0001
Age at first visit −0.0005 0.0640 −0.0006 0.0183
PPS at first visit 0.52 <0.0001 0.54 <0.0001
Visit number 0.008 0.0137 0.006 0.0260
Gender   0.9440    
 Female −0.0003 0.9738    
 Male (reference) 0    
Visit site   <0.0001   <0.0001
 Forsyth −0.15 <0.0001 −0.13 <0.0001
 Four Seasons 0.05 0.0003 0.057 <0.0001
 Hospice of Wake (reference) 0 0
Race   0.2886    
 African American 0.016 0.3133    
 Others −0.034 0.2540    
 White 0    
Reason for referral   0.2774    
 Goals/Decision making −0.004 0.8946    
 Pain/Other symptom management 0.014 0.6295    
 Psychosocial needs 0.019 0.5880    
 EOL issues (reference) 0    
Life expectancy   0.7262    
 Hours to days −0.043 0.3616    
 Days to weeks 0.0096 0.7375    
 Weeks to months 0.014 0.4431    
 4 to 6 months −0.0034 0.7234    
 Greater than 6 months (reference) 0    
Respondent   0.1946   0.0524
 Patient 0.023 0.3059 0.021 0.2250
 Family/Proxy 0.007 0.7590 0.001 0.9525
 Other (reference) 0 0
N 455   587  
R squared 0.60   0.59  

Note: Table shows full model and then model reduced to show only significantly significant predictors. N=293 missing cases due to item missing values for full model; n=161 for reduced.

EOL, end of life; PPS, Palliative Performance Scale.