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The patient/family have the right to exercise his/her rights as a Hospice patient.
Be fully informed of health status unless contradicted by their physician.
Make decisions about health care, including completion of advance directives: a living will, a health care agent, an attorney-in-fact for health care and/or a conservator.
Receive necessary information by designated Hospice staff about services covered (under hospice benefit) to give informed consent prior to being admitted to The Connecticut Hospice, Inc. system to care and/or treatment.
Refuse treatment to the extent permitted by law, and to be informed of possible consequences of his/her decision.
Participate or choose whether to participate in a research study and understand Hospice will protect them and respect their rights during research.
Request a change of caregiver without fear of consequences.
Request discharge from The Connecticut Hospice program or choose non-hospice care (for example: hospice care outside the plan of care) and transfer to another system of care, or care by family.
Receive complete information/explanation concerning needs for an alternative to such a transfer. Hospice must provide evaluation, service and referral as indicated by the patient’s situation.
Expect access to information delineating the process of registration, review and resolution of patient/family complaints
To ask for more information concerning anything you do not understand.
The patient/family have the responsibility to give The Connecticut Hospice an accurate and complete health history when requested to do so.
The patient/family will be actively involved in developing and implementing a plan of care, which will include the use of all appropriate personnel and community resources.
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