[Code of Federal Regulations]

[Title 42, Volume 3]

[Revised as of October 1, 2005]

From the U.S. Government Printing Office via GPO Access

[CITE: 42CFR489.102]



[Page 960-962]

 

                         TITLE 42--PUBLIC HEALTH

 

  CHAPTER IV--CENTERS FOR MEDICARE & MEDICAID SERVICES, DEPARTMENT OF 

                  HEALTH AND HUMAN SERVICES (CONTINUED)

 

PART 489_PROVIDER AGREEMENTS AND SUPPLIER APPROVAL--Table of Contents

 

                      Subpart I_Advance Directives

 

Sec. 489.102  Requirements for providers.



    (a) Hospitals, critical access hospitals, skilled nursing 

facilities, nursing facilities, home health agencies, providers of home 

health care (and for Medicaid purposes, providers of personal care 

services), hospices, and religious nonmedical health care institutions 

must maintain written policies and procedures concerning advance 

directives with respect to all adult individuals receiving medical care, 

or patient care in the case of a patient in a religious nonmedical 

health care institution, by or through the provider and are required to:

    (1) Provide written information to such individuals concerning--

    (i) An individual's rights under State law (whether statutory or 

recognized by the courts of the State) to make decisions concerning such 

medical care, including the right to accept or refuse medical or 

surgical treatment and the



[[Page 961]]



right to formulate, at the individual's option, advance directives. 

Providers are permitted to contract with other entities to furnish this 

information but are still legally responsible for ensuring that the 

requirements of this section are met. Providers are to update and 

disseminate amended information as soon as possible, but no later than 

90 days from the effective date of the changes to State law; and

    (ii) The written policies of the provider or organization respecting 

the implementation of such rights, including a clear and precise 

statement of limitation if the provider cannot implement an advance 

directive on the basis of conscience. At a minimum, a provider's 

statement of limitation should:

    (A) Clarify any differences between institution-wide conscience 

objections and those that may be raised by individual physicians;

    (B) Identify the state legal authority permitting such objection; 

and

    (C) Describe the range of medical conditions or procedures affected 

by the conscience objection.

    (2) Document in a prominent part of the individual's current medical 

record, or patient care record in the case of an individual in a 

religious nonmedical health care institution, whether or not the 

individual has executed an advance directive;

    (3) Not condition the provision of care or otherwise discriminate 

against an individual based on whether or not the individual has 

executed an advance directive;

    (4) Ensure compliance with requirements of State law (whether 

statutory or recognized by the courts of the State) regarding advance 

directives. The provider must inform individuals that complaints 

concerning the advance directive requirements may be filed with the 

State survey and certification agency;

    (5) Provide for education of staff concerning its policies and 

procedures on advance directives; and

    (6) Provide for community education regarding issues concerning 

advance directives that may include material required in paragraph 

(a)(1) of this section, either directly or in concert with other 

providers and organizations. Separate community education materials may 

be developed and used, at the discretion of providers. The same written 

materials do not have to be provided in all settings, but the material 

should define what constitutes an advance directive, emphasizing that an 

advance directive is designed to enhance an incapacitated individual's 

control over medical treatment, and describe applicable State law 

concerning advance directives. A provider must be able to document its 

community education efforts.

    (b) The information specified in paragraph (a) of this section is 

furnished:

    (1) In the case of a hospital, at the time of the individual's 

admission as an inpatient.

    (2) In the case of a skilled nursing facility at the time of the 

individual's admission as a resident.

    (3)(i) In the case of a home health agency, in advance of the 

individual coming under the care of the agency. The HHA may furnish 

advance directives information to a patient at the time of the first 

home visit, as long as the information is furnished before care is 

provided.

    (ii) In the case of personal care services, in advance of the 

individual coming under the care of the personal care services provider. 

The personal care provider may furnish advance directives information to 

a patient at the time of the first home visit, as long as the 

information is furnished before care is provided.

    (4) In the case of a hospice program, at the time of initial receipt 

of hospice care by the individual from the program.

    (c) The providers listed in paragraph (a) of this section--

    (1) Are not required to provide care that conflicts with an advance 

directive.

    (2) Are not required to implement an advance directive if, as a 

matter of conscience, the provider cannot implement an advance directive 

and State law allows any health care provider or any agent of such 

provider to conscientiously object.

    (d) Prepaid or eligible organizations (as specified in sections 

1833(a)(1)(A) and 1876(b) of the Act) must meet the



[[Page 962]]



requirements specified in Sec. 417.436 of this chapter.

    (e) If an adult individual is incapacitated at the time of admission 

or at the start of care and is unable to receive information (due to the 

incapacitating conditions or a mental disorder) or articulate whether or 

not he or she has executed an advance directive, then the provider may 

give advance directive information to the individual's family or 

surrogate in the same manner that it issues other materials about 

policies and procedures to the family of the incapacitated individual or 

to a surrogate or other concerned persons in accordance with State law. 

The provider is not relieved of its obligation to provide this 

information to the individual once he or she is no longer incapacitated 

or unable to receive such information. Follow-up procedures must be in 

place to provide the information to the individual directly at the 

appropriate time.



[57 FR 8203, Mar. 6, 1992, as amended at 59 FR 45403, Sept. 1, 1994; 60 

FR 33294, June 27, 1995; 62 FR 46037, Aug. 29, 1997; 64 FR 67052, Nov. 

30, 1999; 68 FR 66720, Nov. 28, 2003]