78OAG208
78OAG208
Cite as 78 Md. Op. Att'y Gen. 208
208
The law as it existed prior to the enactment of Chapter 372 is
1
discussed in Mack v. Mack, 329 Md. 188, 618 A.2d 744 (1993), with
respect to life-sustaining treatment issues in a guardianship for a patient
in a persistent vegetative state, and in two earlier Opinions of the Attorney
General, 73 Opinions of the Attorney General 162 (1988) and 75 Opinions
of the Attorney General 253 (1990) with respect to life-sustaining
treatment issues generally.
HEALTH
LIFE-SUSTAINING PROCEDURES — INTERPRETATION OF HEALTH
CARE DECISIONS ACT
June 1, 1993
The Honorable William Donald Schaefer
Governor of Maryland
We are writing to discuss a number of interpretive issues
presented by Chapter 372 (House Bill 1243) of the Laws of
Maryland 1993, which adds to the Health-General Article of the
Maryland Code (“HG” Article) a new “Health Care Decisions Act,”
effective October 1, 1993. We had previously addressed many of
these issues in our bill review letter of May 7, 1993, in which we
approved the legislation for constitutionality and legal sufficiency.
Because of the importance of the Act and our desire to give wide
circulation to these interpretations of it, we are reissuing the bill
review letter in this revised format, with additional discussion.
I
Background
Chapter 372 is a comprehensive reform of health care decision
making law in Maryland. It has four major components: provisions
1
on advance directives that expand the means by which an individual
may make decisions about future medical contingencies and that
confirm an individual’s right to designate a health care agent;
provisions that authorize surrogate decision making on behalf of
209
The legislative history warrants further brief explanation. Four
2
comprehensive bills on the subject of health care decision making were
introduced in the 1993 Session: House Bill 1243 and Senate Bill 676,
identical bills that largely reflected the recommendations of a drafting
group working under the auspices of the Conference of Circuit Judges and
chaired by Judge John Carroll Byrnes; and House Bill 1432 and Senate
Bill 664, similar bills that reflected the recommendations of a drafting
group chaired by Professor Diane Hoffmann, of the University of
Maryland Law School.
The House and the Senate then decided to craft compromise
legislation, using as a starting point the texts of House Bill 1432 and
Senate Bill 664. Eventually, the compromise was embodied in House Bill
1243, which you signed into law as Chapter 372, and Senate Bill 664,
which you vetoed.
In Cruzan v. Director, Missouri Dep’t of Health, 497 U.S. 261
3
(1990), all of the Justices save one accepted the premise that a competent
patient’s right to refuse life-sustaining treatment was a protected “liberty”
interest under the Fourteenth Amendment. In Mack v. Mack, the Court of
Appeals found that the right to refuse treatment was a common law right,
and therefore the Court “found no need to opine beyond a common-law
analysis ....” 329 Md. at 211.
incapacitated patients who did not designate a health care agent,
subject to certain standards and limitations; provisions that establish
standards and procedures for life-sustaining treatment issues in
guardianship cases; and provisions that specify certain rights, duties,
and immunities of health care providers.
This legislation was the subject of intense debate even before
the Session began, very exacting attention from the House
Environmental Matters and Senate Judicial Proceedings Committees,
and an ultimate compromise that incorporated elements of one bill
into another. The Health Care Decisions Act gives primacy, as it
2
must, to an individual’s constitutionally protected right to health care
autonomy. The Act also reflects the policy judgment that family
3
and other “surrogate decision makers” should have broad, but not
limitless, authority to make decisions on behalf of patients who are
unable to decide for themselves and who did not choose a decision
maker in an advance directive. Further, the Act respects the
professional integrity of physicians and other health care providers
by, for example, codifying a physician’s right to decline to provide
210
This grant of authority to physicians is subject to an exception
4
when a patient or other authorized decision maker instructs that life-
sustaining procedures be provided. HG §5-613(a)(3).
We have also identified two minor textual errors in Chapter 372,
5
which should be addressed in next year’s corrective bill:
1.
The bill contains an erroneous cross-
reference. On page 36, in line 13, “§5-
606(c)” should read “§5-605(c).”
2.
On page 32, in line 21, the word “result”
should read “results.”
“ethically inappropriate” or “medically ineffective” treatment. HG
§5-611.
4
Yet the Act retains an overall balance through its articulation
of standards and a series of provisions that protect patients against
potentially harmful decisions by others. For example, health care
providers have a specific duty to act to protect an incapacitated
patient if an instruction to withhold or withdraw a life-sustaining
procedure is believed to be “inconsistent with generally accepted
standards of patient care ....” HG §5-612(a). The balanced approach
desired by the Legislature is reflected in a preamble, which states
that the intent of the Act is to ensure an individual’s right to
“personal health care decision making”; to honor the societal value
that every individual’s life “has worth in and of itself, and is not to
be devalued by reason of an individual’s incapacity or perceived
diminished ‘quality of life’ ...”; and to afford “reasonable
safeguards” so that decision making on behalf of incapacitated
persons is focussed solely on their wishes and interests.
With an eye toward these overall legislative goals, this opinion
is intended to resolve certain issues of interpretation that have arisen
since the passage of the Act.
5
211
A health care agent’s authority to withhold or withdraw life-
6
sustaining procedures may be limited by the individual who appoints the
agent to those three circumstances or any others, but the agent’s authority
is not so limited by the statute. See HG §§5-602(b)(1) and 5-606(b).
For a discussion of the meaning of the undefined term “imminent,”
7
see 73 Opinions of the Attorney General at 168.
The definition, recognizing that different causative factors will
8
require different periods of observation and testing before this diagnosis
can be made with confidence, calls for “the passage of a medically
appropriate period of time” before a certification that the condition truly
is irreversible. HG §5-601(o)(2). The certification process for persistent
vegetative state requires the participation of one physician with”special
expertise in the evaluation of cognitive functioning ....” HG §5-606(b)(2).
II
“End-Stage Condition”
An individual may use an advance directive, written or oral, to
decide against the use of life-sustaining procedures under three
circumstances: “terminal condition,” “persistent vegetative state,”
or “end-stage condition.” A surrogate’s authority to withhold or
withdraw life-sustaining procedures likewise is limited to those three
circumstances, as certified by two physicians. HG §5-606(b).
6
The most familiar of these terms, because it is used and defined
in the current Living Will Law, is “terminal condition.” Under the
definition in HG §5-601(q), just as under current law, a patient may
not be certified to be in a “terminal condition” unless two physicians
agree that death from an incurable condition is “imminent.”
7
The term “persistent vegetative state” is new to Maryland law
but is a well-established clinical term. As defined in HG §5-601(o),
a “persistent vegetative state” exists only if the patient “has suffered
a permanent loss of consciousness, exhibiting no behavioral
evidence of self-awareness or awareness of surroundings ....” As
8
the Court of Appeals described the condition in Mack v. Mack, 329
Md. 188, 192, 618 A.2d 744 (1993):
The distinguishing feature of a patient in a
persistent vegetative state is wakefulness
212
without awareness. These patients commonly
make sporadic movements, spontaneously
blink their eyes, and have heightened reflex
responses, but they cannot voluntarily respond
to stimuli.
The last of the three categories, “end-stage condition,” was
perhaps the most controversial element in the legislation and
therefore was the object of special legislative focus. Ultimately, the
definition was framed in HG §5-601(i) as follows:
“End-stage
condition”
means
an
advanced, progressive, irreversible condition
caused by injury, disease, or illness:
(i) That has caused severe and permanent
deterioration indicated by incompetency and
complete physical dependency; and
(ii) For which, to a reasonable degree of
medical certainty, treatment of the irreversible
condition would be medically ineffective.
Unlike a patient in a terminal condition, a patient in an end-
stage condition does not face “imminent” death, although the
condition must be “advanced, progressive, and irreversible.” And
unlike a patient in a persistent vegetative state, a patient in an end-
stage condition does not suffer a total loss of consciousness,
although the condition must have caused “severe and permanent
deterioration.”
The
hallmarks
of
this
deterioration
are
specified:
“incompetency” and “complete physical dependency.” The term
“incompetency” is not defined, but in context it refers to the patient’s
inability to understand or evaluate treatment issues. See HG §5-
601(1) (definition of “incapable of making an informed decision”).
The meaning of the key phrase “complete physical
dependency” should be understood in light of the overall purpose of
the definition of “end-stage condition”: to describe those patients
213
HG §19-301(k) contains an itemization of “personal care”
9
activities that can guide physicians in assessing whether a patient’s
deterioration has reached the stage of “complete physical dependency.”
who are suffering from progressive and incurable diseases like
Alzheimer’s disease or AIDS and on whom the disease has already
exacted a severe toll. The “end-stage” of such diseases will have
arrived only when the patient’s physical deficits are such that the
patient is generally unable to perform independently a broad range
of activities of daily living. According to the Senate Floor Report on
House Bill 1243, the Senate’s intent in insisting on the language
“complete physical dependency” was “to emphasize that the category
of ‘end-stage condition’ only applies to patients who have suffered
severe and permanent generalized infirmity from an untreatable
irreversible condition.”
Thus, on the one hand, a patient with Alzheimer’s disease who
needs help with some aspects of personal care but who is able to
engage in other activities independently is not in an “end-stage
condition.” On the other hand, an Alzheimer’s disease patient who
has deteriorated to the point where the patient needs help in all
aspects of personal care might be determined to be in an “end-stage
condition.” A representative of the Medical and Chirurgical Faculty
9
of Maryland well summarized the legislative objective underlying
this language:
With regard to the “end-stage condition”
definition, the use of “complete” to modify
“physical dependency” is evidently aimed at
describing victims of Alzheimer’s Disease and
other conditions, who are bed-ridden and
suffering from a generalized infirmity that will
not improve. A physician who is asked to
evaluate whether a patient has experienced
“complete physical dependency” would look
to the range of ordinary physical abilities and
assess the patient’s ability to conduct them
independently.
Letter to Delegate Stephen J. Braun from Angus R. Everton, Esquire
(April 2, 1993).
214
The witness requirements are significantly more relaxed than
10
under the current Living Will Law. Under HG §5-602(c), “any competent
individual” may witness an advance directive, “including an employee of
a health care facility or physician caring for the [patient] if acting in good
faith.” Only a health care agent for the patient is flatly barred from
serving as a witness, although at least one of the two witnesses to a written
advance directive must be financially disinterested. An oral advance
directive must be made in the presence of the patient’s attending physician
and one witness. HG §5-602(d).
Finally, treatment of the underlying condition must be
“medically ineffective.” If a treatment would likely “prevent or
reduce the deterioration” in the patient’s health that the condition
would otherwise cause, then the patient is not in an “end-stage
condition.” See HG §5-601(n) (definition of “medically ineffective
treatment”). But if the underlying condition is, in the phrase of the
Senate Floor Report, “untreatable,” the last element of the definition
will have been met.
III
Clarifications in Forms
Chapter 372 repeals the current Living Will Law and creates
a new type of health care planning instrument called an “advance
directive.” The advance directive encompasses both documents that
contain instructions, like a living will, and documents that select a
decision maker, like a durable power of attorney for health care. No
particular form is required; the only formality is the requirement for
two witnesses to a written advance directive. The Act
10
“grandfathers” existing documents: All existing living wills, durable
powers of attorney for health care, and similar documents remain
valid. HG §§5-614(d) and 5-616(b).
Although no forms are required, the Act provides optional
forms as an accommodation to those who do not wish to have
documents drafted by a lawyer. The first of the two optional forms,
called “Form I,” is a more traditional living will, intended as a
limited instructional document for decisions about life-sustaining
procedures in the event of terminal condition or persistent vegetative
state (not for end-stage condition). The other optional form, called
“Form II,” contains two parts: Part A allows for the appointment of
215
a health care agent; Part B gives instructions about health care
issues, including decisions about life-sustaining procedures in the
event of terminal condition, persistent vegetative state, and end-stage
condition.
An inadvertent misplacement of certain language, however,
might lead to confusion about the scope of these two optional
advance directive forms. The language in question deals with the
issue of pregnancy and its potential effect on decision making in an
advance directive.
Under the current Living Will Law, a living will may not be
implemented if an otherwise qualified patient is pregnant. HG §5-
605(2). In its provisions on advance directives, Chapter 372 reflects
a policy decision to eliminate this kind of mandatory provision and
instead allow a woman to decide for herself whether pregnancy
would have any effect on decision making under an advance
directive. The Floor Report on House Bill 1243 explains that
“[e]ach form contains a provision allowing a woman to provide
specific instructions to a health care agent or to a health care
practitioner as to how to proceed if she is pregnant at the time the
advance directive becomes effective.”
The text of the optional forms in Chapter 372 does not
properly carry out this objective. As explained above, Form I, the
living will is not a document by which an individual appoints a
health care agent. Yet on page 37, lines 25-26 of Chapter 372, Form
I contains the following language: “If I am pregnant my agent shall
follow these specific instructions: ....” This language is in the wrong
place; it actually belongs in Part A of Form II, which is the optional
form for appointment of a health care agent. In the living will form,
Form I, the same language should have been set out as correctly
appears in Part B of Form II (page 40, lines 40-41): “If I am
pregnant, my decision concerning life-sustaining procedures shall be
modified as follows: ....” Had this language appeared as well in
Form I, the legislative purpose of having “[e]ach form” contain an
opportunity for instructions about pregnancy would have been
effectuated.
When the Attorney General’s Office distributes to the public
the optional statutory forms, we intend to correct the forms so that
the intended language appears in each place, thus reflecting the
216
actual legislative purpose. See Kaczorowski v. City of Baltimore,
309 Md. 505, 525 A.2d 687 (1987). We suggest that the law be
amended next session to correct the error.
One other provision in the optional forms needs clarification.
Part B of Form II allows a declarant to make a range of health care
decisions, including a decision about medication for the relief of
pain: “I direct that no matter what my condition, medication not be
given to me to relieve pain and suffering, if it would shorten my
remaining life.” The antecedent of the pronoun “it” is not entirely
clear from the sentence structure. The intention is to refer to the
administration of medication. That is, some medications for the
relief of pain have the effect of depressing respiration and therefore
of increasing the risk of an earlier death than would occur if the
medication were not administered. This provision in the form allows
an individual to choose to forgo pain relief if the medication would
likely present that risk. An individual who does not initial that
provision will be opting for the provision of pain relief in
accordance with customary medical practice.
IV
Surrogate Decision Making
A.
Guardian as Surrogate
HG §5-605(a)(2) contains the following priority ranking of
surrogate decision makers:
(i)
A guardian for the patient, if one has been
appointed;
(ii) The patient’s spouse;
(iii)
An adult child of the patient;
(iv) A parent of the patient;
(v) An adult brother or sister of the patient;
or
217
The “requirements of paragraph (3)” refer to an affidavit
11
demonstrating “the specific facts and circumstances” of “regular contact
with the patient sufficient to be familiar with the patient’s activities,
health, and personal beliefs.” HG §5-605(a)(3)(ii).
Someone who is only a guardian of the estate of a disabled person
12
is not a “guardian for the patient” within the meaning of HG §5-605(a)(2).
(vi) A friend or other relative of the patient
who meets the requirements of paragraph
(3) of this subsection.11
A surrogate decision maker is generally authorized to make health
care decisions for a patient “who has been certified to be incapable
of making an informed decision and who has not appointed a health
care agent ....” HG §5-605(a)(2). Someone who is ranked lower in
the priority order may make a decision “only if all individuals in the
next higher class are unavailable.” Id. Thus, “[a] guardian for the
patient, if one has been appointed,” trumps all other potential
surrogates.
In our view, the term “guardian for the patient” means a
guardian of the person of the patient to whom the court has given
power to consent to medical care under §13-708(b)(8) of the Estates
and Trusts Article (“ET” Article). The court is instructed by statute
12
to grant the guardian “only those powers necessary to provide for the
demonstrated need of the disabled person.” ET §13-708(a). A
court’s decision not to grant a guardian power over health care
matters, therefore, reflects a determination that the exercise of such
power by the guardian is not necessary for the needs of the disabled
person. Moreover, “[t]he administration of guardianship affairs
remains subject to judicial control by the equity court that appointed
the guardian.” Mack v. Mack, 329 Md. 188, 201, 618 A.2d 744
(1993). See also Kircherer v. Kircherer, 285 Md. 114, 118, 400
A.2d 1097 (1979). The General Assembly cannot reasonably be
taken to have undermined this fundamental principle by giving
authority to a guardian to act on health matters when the court itself
chose not to grant such authority.
As we read it, the priority among surrogates assigned the
guardian by HG §5-605(a)(2)(i) is predicated on the court’s grant of
authority over health care matters to the guardian. If a guardian of
218
With respect to life-sustaining procedures, the guardian is subject
13
not only to these standards but also the requirements of ET §13-708(c) and
any conditions imposed by the court. See Part VII below.
the person has not been given power over health care matters
pursuant to ET §13-708(b)(8), another surrogate, if one is available,
may make health care decisions for the patient. If no surrogate is
available, the guardian of the person should seek to be granted
power under ET §13-708(b)(8).
Our construction ) that the priority rank among surrogates
accorded to the guardian does not give the guardian any authority
beyond that granted by the court ) by no means renders the surrogate
priority provision meaningless. The priority avoids potential
confusion if someone lower in the priority list is the guardian.
Suppose, for example, that the patient’s spouse is available to make
health care decisions, but the patient’s parent is the guardian of the
person of the patient, vested by the court with authority to make such
decisions. Ordinarily, the spouse has priority over a parent. In this
example, however, the priority accorded the guardian by HG §5-
605(a)(2)(i) ensures that the parent will be the recognized decision
maker.
Furthermore, the designation of the guardian as surrogate
ensures that the guardian is subject to proper standards when making
health care decisions generally. Although Chapter 372 contains
detailed provisions governing the responsibility of the guardian and
the court when issues about life-sustaining procedures arise, neither
the new law nor existing statutory provisions about guardianship
delineate standards for the other kinds of health care decisions
encompassed by ET §13-708(b)(8). The designation of the guardian
as surrogate means that the guardian, like all other surrogates, is
subject to the standards in HG §5-605(c). These standards require
a surrogate to base decisions solely “on the wishes of the patient and,
if the wishes of the patient are unknown or unclear, on the patient’s
best interest”; and, conversely, to refrain from basing decisions
about life-sustaining procedures on the patient’s “pre-existing, long-
term mental or physical disability, or ... economic disadvantage.”13
219
Hospitals and related institutions are required by law to establish
14
patient care advisory committees. HG §19-371(a). Chapter 372 does not
affect the right of any “petitioner” to bring a matter to the committee. See
HG §§19-370(d), 19-373(a), and 19-374(a).
B.
Disputes Among Surrogates
If individuals with equal claim to be surrogates disagree about
a health care decision on behalf of an incapacitated patient and the
patient is in a facility with a patient care advisory committee, the
dispute must be referred to the committee by the patient’s attending
physician or a surrogate. HG §5-605(b). The subsection goes on
14
to provide that the attending physician “may act in accordance with
the recommendation of the committee or transfer the patient in
accordance with the provisions of HG §5-613 of this subtitle.”
When the initial Senate version of the Health Care Decisions
Act, Senate Bill 664, was introduced, this provision was drafted as
a mandate: The physician “shall act in accordance with the
recommendation of the committee or transfer the patient ....” Senate
Bill 664, page 16, line 25. Under this language, the physician would
have been obliged to do one thing or the other. After objections
from those who believed that such a mandate was inconsistent with
the advisory nature of these committees, the word “shall” was
changed to “may,” as it was in House Bill 1432, the initial House
version of the Health Care Decisions Act. As a result, the physician
is not obliged to do either; the physician may accede to the
committee’s recommendation (in which case HG §5-605(b) accords
the physician limited immunity), transfer the patient, or take any
other action authorized by law.
V
EMS “Do Not Resuscitate Orders”
The bill contains a provision, HG §5-608, authorizing certified
emergency medical services personnel to follow certain “emergency
medical services ‘do not resuscitate orders.’” One of the
circumstances under which these DNR orders are to be followed is
“in accordance with protocols established by the Maryland Institute
for Emergency Medical Services Systems in conjunction with the
State Board of Physician Quality Assurance.” HG §5-608(a). Under
220
The title of House Bill 1243 does not contain explicit language
15
reflecting this provision. (By contrast, in the title of Senate Bill 664, this
provision was reflected explicitly in the phrase “requiring a health care
facility to provide certain information.”) However, the title of House Bill
1243 does refer to “establishing certain duties of health care providers
under certain circumstances.” Page 2, lines 38-39. Because a health care
facility is a “health care provider,” see HG §5-601(k), the title reference
in House Bill 1243 is constitutionally sufficient, in our judgment.
Chapter 592 (House Bill 1222) of the Laws of Maryland 1993, these
“protocols” would be developed by the new State Emergency
Medical Services Board. See §13-1D-09(a) and (b)(1)(ii) of the
Education Article (to be effective October 1, 1993).
The other two circumstances under which emergency medical
services personnel are to follow these DNR orders involve oral
orders by a physician, either an on-line command and control
physician or a physician physically present on the scene with the
patient. HG §5-608(c)(2) and (3). Although this provision
authorizes EMS personnel to follow the physician’s orders in such
circumstances, it does not itself provide any new authority to the
physician to issue such an order. A physician who issues a DNR
order to EMS personnel must have a basis for doing so elsewhere in
the bill ) for example, if the physician were implementing the
patient’s prior oral advance directive.
VI
Distribution of Information
HG §5-615 requires every “health care facility,” as defined in
HG §19-101, to “provide each individual on admittance to the
facility information concerning the rights of the individual to make
decisions concerning health care, including the right to accept or
refuse treatment, and the right to make an advance directive,
including a living will.”
15
Under the federal Patient Self-Determination Act, hospitals,
nursing homes, health maintenance organizations, home health
agencies, and hospices that receive Medicare or Medicaid funds
must provide comparable information to their patients. See §§4206
221
and 4751 of the Omnibus Budget Reconciliation Act of 1990, Pub.
L.No. 101-508; 57 Fed. Reg. 8194 (March 6, 1992). The apparent
purpose of HG §5-615 is to extend the requirements of the federal
Act to all health care facilities. For example, an “ambulatory
surgical facility” is a “health care facility” as defined in HG §19-
101(e)(1)(iii) and is therefore covered by the new information
disclosure requirement, even though such facilities are not covered
by the federal Act.
In our view, a health care facility that already complies with
the federal Patient Self-Determination Act need take no additional
actions in order to comply with HG §5-615 as well. A facility that
is not covered by the federal Act but will be required after October
1, 1993, to comply with HG §5-615 may look to the federal Act and
its regulations for guidance. An out-patient facility covered by HG
§5-615, for example, will comply if it makes the required
information available to patients when they initially receive care.
This office will be drafting, and circulating for comment, a
revision of the summary of State law required by the Patient Self-
Determination Act, to account for the changes in Maryland law
brought about by this legislation.
VII
Standards for Guardians
Under current law, a guardian of the person is required to
obtain authorization from the court prior to consenting to the
provision, withholding, or withdrawal of a “medical procedure that
involves, or would involve, a substantial risk to the life of the
disabled person.” ET §13-708(c). This provision has been
understood to mean that a court must review contemporaneously the
guardian’s proposed decision about the particular life-sustaining
treatment, even though the guardian might have been authorized
initially to decide all health care issues for the ward. Chapter 372
adds the following exception to this general requirement:
222
The court may, upon such conditions as
the court considers appropriate, authorize a
guardian to make a decision regarding medical
procedures that involve a substantial risk to
life without further court authorization, if:
(i) The disabled person has executed an
advance directive in accordance with Title 5,
Subtitle 6 of the Health-General Article that
authorizes the guardian to consent to the
provision, withholding or withdrawal of a
medical procedure that involves a substantial
risk to life but does not appoint a health care
agent; or
(ii) The guardian is also the disabled
person’s spouse, adult child, parent, or adult
brother or sister.
ET §13-708(c)(2). The phrase “further court authorization” implies
that the court may grant this authorization prior to the time that the
actual treatment decision must be made. For example, the court
might include in the order appointing a guardian a provision
authorizing the guardian to decide certain issues about life-
sustaining procedures. If the court chose to do so, the guardian
would not need to file a subsequent petition seeking the court’s
authorization for a decision within the scope of the initial order.
The first of the two subparagraphs describing the
circumstances when the court may permit this advance authorization
describes a pertinent decision made by the now disabled person in an
advance directive. The responsibility of the guardian under such
circumstances is that of any other decision maker when an individual
has executed an advance directive ) to carry out the wishes of the
individual as expressed in the document.
The question has arisen, however, as to the standards
applicable to the decision of a guardian who has been given advance
authorization by the court because of the guardian’s status as “the
disabled person’s spouse, adult child, parent, or adult brother or
sister.” To be sure, such a guardian is subject to whatever conditions
“the court considers appropriate.” Nevertheless, the question is
223
See note 13 above and accompanying text.
16
whether the guardian would be subject to any statutorily defined
standard apart from the conditions imposed by the court, if, for
example, a court’s advance authorization were silent about
decisional standards.
A patient’s spouse, adult child, parent, or adult brother or sister
is given priority in the classes of surrogate decision makers set out
in HG §5-605(a)(2). The amendment to ET §13-708(c) reflects a
legislative judgment that, in effect, these close family members may
be permitted by the court to act in their capacity as surrogate
decision makers. In our view, then, these guardians are subject to
the standards for surrogate decision making set out in HG §5-605(c),
whether or not the court imposes any conditions. A reading of the
16
provision that would permit these guardians to act on any other basis
would be inconsistent with the General Assembly’s intent, expressed
in the preamble, “that this Act advance the interests and wishes of
the individuals whose life and health may be affected by its
provisions, not the interests and wishes of others, including those
who are granted authority under this Act to act on behalf of an
individual.”
VIII
Conclusion
When this office first undertook its involvement in issues
relating to life-sustaining treatment, we wrote that “[t]hese decisions
are forged out of personal emotions, medical and ethical judgments,
and religious beliefs. No opinion of the Attorney General can really
go to the heart of the matter.” What we could do, we said, was “to
make clear how the law affects this most private and deeply felt of
decisions.” 73 Opinions of the Attorney General 162 (1988).
The Health Care Decisions Act is an important reform that
clarifies the law and thereby removes at least some small burden
from the patients, families, and health care providers who face these
decisions daily. The Attorney General’s Office is proud of its role
in the development and enactment of this legislation. We look
224
forward to a common effort to make the new law work as the
Legislature intended.
J. Joseph Curran, Jr.
Attorney General
Jack Schwartz
Chief Counsel
Opinions & Advice