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. Author manuscript; available in PMC: 2016 Oct 13.
Published in final edited form as: J Pain Symptom Manage. 2014 Dec 24;49(5):904–15.e1-3. doi: 10.1016/j.jpainsymman.2014.10.018

Table 1.

Content Areas of Surveys and Their Definitions

Content Area Definition
Bereavement support Related to support and services provided to family after death of patient
Caregiver support Related to support and services available or provided to caregiver
Environment Related to room, noise, comfort of facility
Financial needs Related to patient’s financial needs, health care costs, and funeral planning
Information and care
 planning
Related to advance care planning, communication, and decision-making between patient, family & providers,
 discussing goals/preferences for care, information related to informal care for patient at home
Overall experience General assessments of care received; overall experience
Personal care Related to the quality of personal care provided in facility or home (bathing, eating, and so on)
Provider care Related to quality of and satisfaction with care given by specified provider (doctor, nurse, social worker, staff,
 and so on)
Psychosocial care Related to emotional well-being, social support, social needs, and whole-person needs of patient
Quality of death Related to experience of care received immediately before dying for patient/family (e.g., “During the final
 hours of your family member’s life . ”)
Responsiveness and timing Related to responsiveness to needs of patient/caregiver, including availability of hospice staff and timing of
 hospice referral
Spiritual, religious, and
 existential care
Related to religious aspects of care and/or patients’ spiritual/existential needs and well-being
Symptom management Related to experience and management of symptoms such as pain and shortness of breath
Other Demographic information about patient or type of facility (unrelated to satisfaction or experience with care)