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Table 3 Domains of patient- and physician-oriented outcomes by data source

From: Protocol for the “Implementation, adoption, and utility of family history in diverse care settings” study

  

Data source

 

MeTree

Patient surveys

Provider survey

Clinic staff survey (ORIC)

Clinic staff interview

EHR data pull

Emotional

  Satisfaction

 

 

  Barriers to model use

 

   

  Activation

 

    

  Quality of clinical encounter

 

   

  SF-12 (quality of life)

 

    

  Patient activation

 

    

  Knowledge

  

   

  Concur with/quality of CDS

  

   

  ORIC

   

  

  Implementation climate

   

 

Behavioral

  Medication adherence

 

    

  Lifestyle

 

    

  Rec uptake

 

  

  Discussion of risk/prevention

  

   

  Work flow/processes

    

 

  Implementation policies/practices

   

 

  Intervention values and task fit

   

 

Biological

      

  Demographics

     

  FHH

     

  FHH documentation/ counseling

  

   

  % completion of MeTree

     

  Time to complete MeTree

     

Clinical

  Laboratory data

    

  Screening completed

     

  Complications

     

  Vital signs and weight

    

  # medications

     

  Referrals made

     

  % high-risk patients

     

  % with risk-based screening

    

  % with screening completed

     

  % with disease at goal

     

  Visit length/wait times

  

   

Financial

  Socioeconomic status

 

    

  Medication costs

     

  Office/ER visits/hospitalizations

     

  Impact on family members