top of page
Patient Rights
  1. “To be informed of these rights, as evidenced by the patient or their representative, guardian, or surrogate’s written acknowledgment, or by documentation by staff in the medical record, that the patient was offered a written copy of these rights and given a written or verbal explanation of these rights, in terms the patient could understand. The facility shall have the means to notify patients of any rules and regulations it has adopted governing patient conduct in the facility.”

  2. “To be informed of services available in the facility, of the names and professional status of the personnel providing and/or responsible for the patient’s care, and of fees and related charges, including the payment, fee, deposit, and  refund policy of the facility and any charges for services not covered by sources of third-party payment or not covered by  the facility’s basic rate.”

  3. “To be informed if the facility has authorized other health care and educational institutions to participate in the patient’s treatment. The patient or their representative, guardian or surrogate shall also have a right to know the identity and function of these institutions, and to refuse to allow their participation in the patient’s treatment.”

  4. “To receive from the patient’s physician(s) or clinical practitioner(s), in terms that the patient or their representative or surrogate understands, an explanation of his or her complete medical/health condition or diagnosis, recommended treatment, treatment options, including the option of no treatment, risk(s) of treatment, and expected result(s). If this information is detrimental to the patient’s health, or if the patient is not capable of understanding information, the explanation shall be provided to the patient’s representative, guardian, or surrogate. This release of information to their representative, guardian, or surrogate, along with the reason informing the patient directly, shall be documented in the patient’s medical record.”

  5. “To participate in the planning of the patient’s care and treatment and to refuse medication and treatment. Such refusal shall be documented in the patient’s medical record. The patient or their representative, guardian, or surrogate has the right to change primary or specialty physicians if other qualified physicians are available."

  6. “To be included in experimental research only when the patient or their representative, guardian, or surrogate gives informed written consent to such participation, or when a guardian gives consent for an incompetent patient in accordance with law, rule, and regulation. The patient or their representative or surrogate may refuse to participate in experimental research, including the investigation of new drugs and medical devices.”

  7. “To voice grievances or recommend changes in policies and services to facility personnel, the governing body, and/or outside representatives of the patient’s choice either individually or as a group, and free from restraint, interference, coercion, discrimination, or reprisal.”

  8. Advance directives, as required by state or federal law and regulations, and if requested by the patient, the official State advanced directive forms will be provided.

  9. “To be free from mental and physical abuse, free from exploitation, and free from the use of restraints unless they are authorized by a physician for a limited period of time to protect the patient or others from injury. Drugs and other medications shall not be used for discipline of patients or for convenience of facility personnel.”

  10. “To confidential treatment of information about the patient. Information in the patient’s medical record shall not be released to anyone outside the facility without the patient or their representative, guardian or surrogate’s approval, unless another health care facility to which the patient was transferred requires the information, or unless the release of information is required and permitted by law, a third-party payment contract, or a peer review, or unless the information is needed by the New Jersey State Department of Health for statutorily authorized purposes. The facility may release data about the patient for studies containing aggregated statistics when the patient’s identity is masked.”

  11. “To be treated with courtesy, consideration, respect, and recognition of the patient’s dignity, individuality, and right to privacy, including, but not limited to, auditory and visual privacy. The patient’s privacy shall also be respected when the facility personnel is discussing the patient.”

  12. “To not be required to perform work for the facility unless the work is part of the patient’s treatment and is performed voluntarily by the patient. Such work shall be in accordance with local, state, and Federal laws and rules.”

  13. “To exercise civil and religious liberties, including the right to independent personal decisions. No religious beliefs or practices, or any attendance at religious services, shall be imposed upon any patient.”

  14. “To not be discriminated against because of age, race, religion, gender identity, gender. sexuality, nationality, or ability to pay, or deprived of any constitutional, civil, and/or legal rights solely because of receiving services from the facility.”

  15. “To expect and receive appropriate assessment, management, and treatment of pain as an integral component of that person’s care in accordance with N.J.A.C. 8:43E-6.”

bottom of page