Opinion
BLEASE, J.
The California Medical Association and four physicians (collectively referred to as CM A) appeal from a judgment upholding State Department of Health Services regulations which establish procedures for securing informed consent for human sterilization. We hold that the regulations reasonably implement the department’s regulatory authority over unnecessary operations. We affirm the judgment.
Facts
In May of 1977, the California Department of Health (now Department of Health Services) promulgated two regulations establishing procedures for securing informed consent for human sterilization. One governed sterilizations covered by the state’s Medi-Cal scheme (Welf. & Inst. Code, § 14000 et seq.). (Former Cal. Admin. Code, tit. 22, §§ 51163, 51305.1-51305.7, effective Dec. 1, 1977 pursuant to § 51305.8.) The other applied to sterilizations performed in “acute care” hospitals (Health & Saf. Code, § 1250). (Cal. Admin. Code, tit. 22, §§ 70037.1, 70707.1-70707.8, effective Dec. 1, 1977, pursuant to § 70707.9.) Because the issues concerning the Medi-Cal regulations
have become moot,
we are here concerned only with the hospital regulations.
The hospital regulations (as did the Medi-Cal regulations) required that the patient be 18 years of age and competent to “understand the content and nature of the informed consent process” (former Cal. Admin. Code, tit. 22, § 51305.5, subds. (a)(1) and (2); § 70707.5, subds. (a)(1) and (2)), detailing the information to be given to the patient,
in
validating consent given while the patient is in an “altered” mental state or in labor or given less than 24 hours after giving birth or after undergoing an abortion (former Cal. Admin. Code, tit. 22, § 51305.3, subd. (a); § 70707.3, subd. (a)) and, except for “emergency sterilizations[s]”
(id.,
at §§ 51305.1, 70707.1), requiring a 14-day minimum waiting period before a sterilization may be performed unless the patient requested in writing that it be performed sooner, though not sooner than 72 hours
(id.,
at § 51305.2, subd. (a)(2); § 70707.2, subd. (a)(2)). The provisions differed somewhat in the sanctions imposed for noncompliance (possible revocation or suspension of license in the hospital regulations (§ 70707.8) and nonpayment for services under the MediCal regulations (§ 51305.7)), but both provided that noncomplying physicians be reported to the Board of Medical Quality Assurance.
CMA was denied a preliminary injunction and the regulations took effect on December 1, 1977. After hearings on cross-motions for summary judgment, on April 24, 1978, the trial court filed its opinion and order denying CMA’s motion (except as to the provision prohibiting sterilizations for patients under 18 years of age
) and granting the motions of defendants and interveners (respondents). This appeal followed.
After CMA’s opening brief was filed, the Medi-Cal informed consent regulations were amended in response to new federal Medicaid regulations (42 C.F.R. §§ 50.201-50.210). The amended regulations (Cal. Admin. Code, tit. 22, §§ 51163, 51305.1-51305.6), filed June 24, 1980, and effective October 15, 1980, conform to the federal regulations. (Welf. & Inst. Code, § 14191.
)
A short time later, the hospital regulations (Cal. Admin. Code, tit. 22, §§ 70037.1, 70707.1-70707.8) were amended (to continue) to parallel the Medi-Cal regulations. The amended rules differ from the regulations challenged in several respects. They exclude “secondary sterilizations.” (§ 70037.1, subd. (a).) They increase the minimum waiting period to 30 days, waivable to 72 hours in connection with emergency abdominal surgery or premature delivery under the Medi-Cal regulations, and by written request under the proposed hospital regulations. (§ 51305.1, subd. (a)(6); § 70707.1, subd. (a)(4).) The information required to be given patients remains substantially the same as that required under the former regulations. (§§ 51305.3; 70707.4.)
Discussion
I
CMA attacks the (hospital) informed consent regulations as exceeding the regulatory powers of the Department of Health Services over hospitals. (Gov. Code, § 11342.1;
Agricultural Labor Relations Bd.
v.
Superior Court
(1976) 16 Cal.3d 392, 411 [128 Cal.Rptr. 183, 546 P.2d 687];
California Assn. of Nursing Homes etc., Inc.
v.
Williams
(1970) 4 Cal.App.3d 800, 810 [84 Cal.Rptr. 590, 85 Cal.Rptr. 735].) It claims that there is no authority to regulate professional treatment within which it includes the securing of informed consent.
“The task of the reviewing court in such a case ‘“is to decide whether the [agency] reasonably interpreted the legislative mandate.” [Citation.]’
(Credit Ins. Gen. Agents Assn.
v.
Payne
(1976) 16 Cal.3d 651, 657 [128 Cal.Rptr. 881, 547 P.2d 993].)”
(Woods v. Superior Court
(1981) 28 Cal.3d 668, 679 [170 Cal.Rptr. 484, 620 P.2d 1032]; see also
Ralph’s Grocery Co.
v.
Reimel
(1968) 69 Cal.2d 172, 176 [70 Cal.Rptr. 407, 444 P.2d 79];
Morris
v.
Williams
(1967) 67 Cal.2d 733 [63
Cal.Rptr. 689, 433 P.2d 697].) We conclude that the department’s interpretation is reasonable and uphold the hospital regulations.
There is no statute which expressly
states
that the department may adopt informed consent regulations applicable to hospitals (as there is under the Medi-Cal statutes—Welf. & Inst. Code, § 14191) and CMA attempts to exploit this void by a limiting construction of the statutory authority of the department. That authority is to be found in the following statutes.
The Department of Health Services has licensing power over various health facilities including hospitals. (Health & Saf. Code, § 1250 et seq.)
It is given general (§ 208
) and specific (§ 1275
) regulatory authority to carry out its hospital licensing duties and powers and to fulfill the intent of the licensing laws.
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Opinion
BLEASE, J.
The California Medical Association and four physicians (collectively referred to as CM A) appeal from a judgment upholding State Department of Health Services regulations which establish procedures for securing informed consent for human sterilization. We hold that the regulations reasonably implement the department’s regulatory authority over unnecessary operations. We affirm the judgment.
Facts
In May of 1977, the California Department of Health (now Department of Health Services) promulgated two regulations establishing procedures for securing informed consent for human sterilization. One governed sterilizations covered by the state’s Medi-Cal scheme (Welf. & Inst. Code, § 14000 et seq.). (Former Cal. Admin. Code, tit. 22, §§ 51163, 51305.1-51305.7, effective Dec. 1, 1977 pursuant to § 51305.8.) The other applied to sterilizations performed in “acute care” hospitals (Health & Saf. Code, § 1250). (Cal. Admin. Code, tit. 22, §§ 70037.1, 70707.1-70707.8, effective Dec. 1, 1977, pursuant to § 70707.9.) Because the issues concerning the Medi-Cal regulations
have become moot,
we are here concerned only with the hospital regulations.
The hospital regulations (as did the Medi-Cal regulations) required that the patient be 18 years of age and competent to “understand the content and nature of the informed consent process” (former Cal. Admin. Code, tit. 22, § 51305.5, subds. (a)(1) and (2); § 70707.5, subds. (a)(1) and (2)), detailing the information to be given to the patient,
in
validating consent given while the patient is in an “altered” mental state or in labor or given less than 24 hours after giving birth or after undergoing an abortion (former Cal. Admin. Code, tit. 22, § 51305.3, subd. (a); § 70707.3, subd. (a)) and, except for “emergency sterilizations[s]”
(id.,
at §§ 51305.1, 70707.1), requiring a 14-day minimum waiting period before a sterilization may be performed unless the patient requested in writing that it be performed sooner, though not sooner than 72 hours
(id.,
at § 51305.2, subd. (a)(2); § 70707.2, subd. (a)(2)). The provisions differed somewhat in the sanctions imposed for noncompliance (possible revocation or suspension of license in the hospital regulations (§ 70707.8) and nonpayment for services under the MediCal regulations (§ 51305.7)), but both provided that noncomplying physicians be reported to the Board of Medical Quality Assurance.
CMA was denied a preliminary injunction and the regulations took effect on December 1, 1977. After hearings on cross-motions for summary judgment, on April 24, 1978, the trial court filed its opinion and order denying CMA’s motion (except as to the provision prohibiting sterilizations for patients under 18 years of age
) and granting the motions of defendants and interveners (respondents). This appeal followed.
After CMA’s opening brief was filed, the Medi-Cal informed consent regulations were amended in response to new federal Medicaid regulations (42 C.F.R. §§ 50.201-50.210). The amended regulations (Cal. Admin. Code, tit. 22, §§ 51163, 51305.1-51305.6), filed June 24, 1980, and effective October 15, 1980, conform to the federal regulations. (Welf. & Inst. Code, § 14191.
)
A short time later, the hospital regulations (Cal. Admin. Code, tit. 22, §§ 70037.1, 70707.1-70707.8) were amended (to continue) to parallel the Medi-Cal regulations. The amended rules differ from the regulations challenged in several respects. They exclude “secondary sterilizations.” (§ 70037.1, subd. (a).) They increase the minimum waiting period to 30 days, waivable to 72 hours in connection with emergency abdominal surgery or premature delivery under the Medi-Cal regulations, and by written request under the proposed hospital regulations. (§ 51305.1, subd. (a)(6); § 70707.1, subd. (a)(4).) The information required to be given patients remains substantially the same as that required under the former regulations. (§§ 51305.3; 70707.4.)
Discussion
I
CMA attacks the (hospital) informed consent regulations as exceeding the regulatory powers of the Department of Health Services over hospitals. (Gov. Code, § 11342.1;
Agricultural Labor Relations Bd.
v.
Superior Court
(1976) 16 Cal.3d 392, 411 [128 Cal.Rptr. 183, 546 P.2d 687];
California Assn. of Nursing Homes etc., Inc.
v.
Williams
(1970) 4 Cal.App.3d 800, 810 [84 Cal.Rptr. 590, 85 Cal.Rptr. 735].) It claims that there is no authority to regulate professional treatment within which it includes the securing of informed consent.
“The task of the reviewing court in such a case ‘“is to decide whether the [agency] reasonably interpreted the legislative mandate.” [Citation.]’
(Credit Ins. Gen. Agents Assn.
v.
Payne
(1976) 16 Cal.3d 651, 657 [128 Cal.Rptr. 881, 547 P.2d 993].)”
(Woods v. Superior Court
(1981) 28 Cal.3d 668, 679 [170 Cal.Rptr. 484, 620 P.2d 1032]; see also
Ralph’s Grocery Co.
v.
Reimel
(1968) 69 Cal.2d 172, 176 [70 Cal.Rptr. 407, 444 P.2d 79];
Morris
v.
Williams
(1967) 67 Cal.2d 733 [63
Cal.Rptr. 689, 433 P.2d 697].) We conclude that the department’s interpretation is reasonable and uphold the hospital regulations.
There is no statute which expressly
states
that the department may adopt informed consent regulations applicable to hospitals (as there is under the Medi-Cal statutes—Welf. & Inst. Code, § 14191) and CMA attempts to exploit this void by a limiting construction of the statutory authority of the department. That authority is to be found in the following statutes.
The Department of Health Services has licensing power over various health facilities including hospitals. (Health & Saf. Code, § 1250 et seq.)
It is given general (§ 208
) and specific (§ 1275
) regulatory authority to carry out its hospital licensing duties and powers and to fulfill the intent of the licensing laws. In section 1276 it is directed to adopt regulations which “shall prescribe standards of adequacy, safety and sanitation of the physical plant, of staffing with duly qualified licensed personnel, and of services, based on the type of health facility and the needs of the persons served thereby.” (Italics added.) (§ 1276.) It is also
granted enforcement powers (§§ 1277,
1294
) which, as we shall show, support the adoption of regulations.
CMA argues that the statutory scheme limits the scope of the department’s authority to the specific subjects of the hospital licensing statutes contained in division 2, chapter 2, of the Health and Safety Code (§ 1250 et seq.). It characterizes these subjects as the power “(1) to supervise construction and maintenance of the health facility to assure adequacy, safety and sanitation of the plant; (2) to establish minimum credentials for the health facility personnel staff; (3) to insure that the ‘basic’ or ‘special’ services are needed in the community; and (4) to insure that qualified staff and adequate facilities are available before a special or basic services permit will be issued.” CMA views the “evident purpose of the entire chapter ... [as] to insure that substandard and Unnecessary facilities are not licensed, and Sections 1276 and 1277 should be interpreted in that light.” CMA concludes that no authority is granted to regulate the doctor-patient relationship within which it includes matters of informed consent.
At the outset, we observe that the informed consent regulations do not represent a novel assertion of regulatory authority by the department
and that the department has statutorily been recognized as
having competency to regulate sterilization operations. (Welf. & Inst. Code, § 14191; see
ante,
fn. 4.) Moreover, the Legislature has placed at least a portion of the subject of sterilization operations within the hospital licensing statutes. Health and Safety Code section 1258
prohibits the conditioning of hospital sterilization operations by “special nonmedical qualifications” such as “age, marital status and number of natural children.” It also states that “nothing in this section shall prohibit requirements relating to the physical or mental condition [of the patient] or affect the right of the attending physician to counsel or advise his patient as to whether sterilization is appropriate... ,”
These provisions make sterilization operations a subject of statutory concern and suggest that the exception for “requirements relating ... to the physical or mental condition” preserves these matters for regulation by the department. CMA reads section 1258 differently.
CMA contends that portions of the informed consent regulations (e.g., waiting periods and special forms) conflict with section 1258’s prohibition on “nonmedical qualifications.” We disagree. The “nonmedical qualifications” named in the statute—age, marital status, number of children—unambiguously imply that the evil in mind is the use of socio-economic factors to determine whether or not to permit an individual to be sterilized. (See
Selected 1972 Legislation
(1973) 4 Pacific L.J. 679, 680.) No such factors are here present. We agree with the trial
court that the regulations should be characterized as “requirements relating to the [patient’s] mental condition” and that their purpose is to assure that a patient has the “requisite comprehension of the nature and gravity of the operation.”
CMA also claims that the department has no
implied
regulatory authority to adopt informed consent regulations. The claim is premised upon a singular reading of the regulatory statutes, that the department’s regulatory authority is limited to the kind contained in section 208, which authorizes the adoption of regulations “for the execution of [the department’s] duties.” CMA reads “duties” as encompassing only authority which is expressly conferred.
We do not concur in CMA’s diagnosis of terminal regulatory anemia. Rather, an examination of the hospital licensing statutes reveals a robust regulatory scheme. The linchpin of the scheme is section 1275.
(Ante,
fn. 7.) It authorizes the adoption of reasonable rules not only to enable the department “to perform the
duties
conferred upon it” (see also § 208), but also to “exercise [its] powers.” It also sanctions “regulations . . . necessary
or
proper to carry out the
purposes and intent”
of the hospital licensing statutes. (Italics added.) Plainly, these regulatory authorizations exceed those contained in section 208.
We read section 1275’s grant of regulatory authority to aid the exercise of the department’s “powers” as extending to the license revocation provisions of sections 1277 and 1294 and as fulfilling a salutary public purpose. The use of rule-making authority to define the generalized subjects of disciplinary action is superior to the piecemeal case-by-case approach of quasi-adjudicative procedures in defining, in advance of discipline, conduct which is proscribed and in thus avoiding the occasion for revelatory discipline.
Section 1294 provides for hospital license discipline for “[c]onduct inimical to the public health ... in the ... operation of [hospital] services.... ” This provision imports the meaning of a “well defined phrase at common law” (“act injurious to the public health”) which was “specifically directed toward . .. unnecessary operations” performed for an improper purpose.
(People
v.
Rehman
(1967) 253 Cal.App.2d 119, 153-154 [61 Cal.Rptr. 65].) Section 1275 authorizes the adoption of
reasonable regulations in aid of preventing unnecessary operations made the subject of disciplinary action of section 1294. A similar authority appears to be granted by section 1276 which
directs
the adoption of regulations which “shall prescribe standards ... of
services, based on
the type of health facility and
the needs of the persons served
thereby.” (Italics added.) Unnecessary operations manifestly do not further the “needs of persons” served by hospitals.
We hold that section 1275, together with sections 1276 and 1294, authorize the department to adopt reasonable regulations regarding “unnecessary operations.” These sections supply the authority for the adoption of regulations consistent with the legislative concerns of section 1258 regarding sterilization operations. The informed consent regulations are reasonably adapted to the end of preventing unwanted or unconsented to, and hence “unnecessary,”
sterilization operations.
We hold the informed consent regulations are proper and reasonably in aid of the department’s power to revoke the licenses of hospitals which countenance unnecessary surgery.
II
CMA urges that the department’s assertion of rule-making authority over informed consent invades the responsibility of the Board of
Medical Quality Assurance (Bus. & Prof. Code, § 2000 et seq.) which disciplines the conduct of physicians. However, the informed consent regulations create no jurisdictional conflict between the agencies. While they permit sanctions to be imposed against hospitals for their violation, a physician believed to be in violation of them is not subject to discipline by the department but must be reported to the board for appropriate action. (Cal. Admin. Code, tit. 22, § 70707.8
; and see § 51305.7.). CMA’s attempt to erect a wall of separation between the jurisdictions of the two agencies which share divides an area of common concern. Just as “both hospital and physician have common concerns and comparable obligations to the patient,” as counsel for CM A conceded to the trial court, so do the department and the board. We will not hypothesize a jurisdictional conflict between the department and the board where none now appears.
Ill
CMA suggests that because of the fundamental nature of the patient’s decision whether or not to undergo sterilization, the establishment of informed consent procedures must be left to the Legislature, which is the only appropriate body to resolve “truly fundamental issues.”
(Kugler
v.
Yocum
(1968) 69 Cal.2d 371, 376 [71 Cal.Rptr. 687, 445 P.2d 303];
Bayside Timber Co.
v.
Board of Supervisors
(1971) 20 Cal.App.3d 1, 11 [97 Cal.Rptr. 431].) Consequently, they maintain, a narrower construction of the department’s statutory rule-making authority is required to avoid raising the issue of an unconstitutional delegation of power.
(Clean Air Constituency
v.
California State Air Resources Bd.
(1974) 11 Cal.3d 801, 816-818 [114 Cal.Rptr. 577, 523 P.2d 617].)
CMA’s argument is based on the mistaken assumption that the presence of “fundamental rights” necessarily predicates “truly fundamental issues.” Rights are “fundamental” or not based on their place in our constitutional scheme; decisions involving procreation are “fundamental” in this sense.
(Roe
v.
Wade
(1973) 410 U.S. 113, 152-153 [35 L.Ed.2d 147, 176-177, 93 S.Ct. 705].)
While the importance of the interests affected may be a determinant of whether an issue is “truly fundamental,” the critical question is whether the Legislature has made a basic policy decision which provides a standard or guide for the exercise of administrative discretion. We do not view the department’s decision to promulgate regulations as one on a “truly fundamental issue” because of the existence of statutory standards governing the department’s exercise of discretion (§§ 1258, 1275, 1276, 1294, subd. (d)) and patients’ needs in regard to hospital services (§ 1276). (See
Kugler
v.
Yocum, supra,
69 Cal.2d at pp. 376-377.) “Merely because a statute empowers an administrative agency to exercise a judgment of high order in implementing legislative policy does not mean that the agency has been given unrestricted powers.”
{City of Santa Ana
v.
City of Garden Grove
(1979) 100 Cal.App.3d 521, 529 [160 Cal.Rptr. 907].)
IV
CMA last argues that the regulations are unnecessary.
CMA advances the extraordinary thesis that the hospital regulations are not “reasonably necessary” because a patient sterilized without his or her informed consent can recover damages for negligence under the rule of
Cobbs
v.
Grant
(1972) 8 Cal.3d 229 [104 Cal.Rptr. 505, 502 P.2d 1]. The merit in the principle by which recovery for an injury is exalted over prevention of an injury wholly escapes us. We can discern nothing that is “arbitrary or capricious,” in the department’s preference for an approach calculated to
prevent
unconsented-to sterilizations over a tort remedy.
The trial court correctly rejected, on the ground that CMA failed to disclose its evidentiary basis, CMA’s argument that the regulations are
too broad to be supported by the evidence adduced at the hearings, which it characterized as establishing that some abuses had occurred.
The judgment is affirmed.
Regan, Acting P. J., and Reynoso, J., concurred.