T—Time |
At least 60 minutes/month of time (per patient and caregiver preference) devoted to palliative care treatments for the patient and family. |
E—Education |
Patients and family members, per their desires and wishes, are counseled and educated about their disease, including self-management of symptoms, prognosis, and treatment options. |
A—Assessment |
Formal assessment of symptoms, including pain, dyspnea, constipation/diarrhea, anxiety/depression, fatigue, and nausea. |
M—Multidisciplinary |
Access to a multidisciplinary palliative care team composed of nurse, physician, social worker, pharmacist, and/or chaplain team members. |