act-2002-0-225•Pennsylvania Act 2002-225 — OPTOMETRIC PRACTICE AND LICENSURE ACT - AMEND PHARMACEUTICAL AGENT REQUIREMENTS FOR GLAUCOMA TREATMENT AND DRUG APPROVAL
Pennsylvania Act 2002-225 — OPTOMETRIC PRACTICE AND LICENSURE ACT - AMEND PHARMACEUTICAL AGENT REQUIREMENTS FOR GLAUCOMA TREATMENT AND DRUG APPROVAL
act-2002-0-2252002 Pa. Act 225Law
Act text
OPTOMETRIC PRACTICE AND LICENSURE ACT - AMEND PHARMACEUTICAL AGENT
REQUIREMENTS FOR GLAUCOMA TREATMENT AND DRUG APPROVAL
Act of Dec. 16, 2002, P.L. 1950, No. 225 Cl. 63
Session of 2002
No. 2002-225
SB 831
AN ACT
Amending the act of June 6, 1980 (P.L.197, No.57), entitled "An
act regulating the licensure and practice of optometry,
making repeals and providing penalties," further defining
"examination and diagnosis" and "practice of optometry"; and
providing for requirements concerning pharmaceutical agents
for the treatment of glaucoma and for approval of drugs.
The General Assembly of the Commonwealth of Pennsylvania
hereby enacts as follows:
Section 1. The definitions of "examination and diagnosis"
and "practice of optometry" in section 2 of the act of June 6,
1980 (P.L.197, No.57), known as the Optometric Practice and
Licensure Act, amended October 30, 1996 (P.L.721, No.130), are
amended to read:
Section 2. Definitions.
The following words and phrases when used in this act shall
have, unless the context clearly indicates otherwise, the
meanings given to them in this section:
* * *
"Examination and diagnosis." Any examination or diagnostic
means or method compatible with optometric education and
professional competence. The term shall encompass the use of
pharmaceutical agents for diagnostic purposes classified as
miotics, mydriatics, cycloplegics, topical anesthetics and dyes
when applied topically to the eye, which pharmaceutical agents
shall be approved by the Secretary of Health as provided in
section 4.3 and, subject to the rules and regulations of the
board, provided however that with respect to optometrists
licensed before March 1, 1974, only such optometrists who have
satisfactorily completed a course in pharmacology as it applies
to optometry, with particular emphasis on the topical
application of diagnostic pharmaceutical agents to the eye,
approved by the board shall be permitted to use diagnostic
pharmaceutical agents topically in the practice of optometry.
* * *
"Practice of optometry."
(1) The use of any and all means or methods for the
examination, diagnosis and treatment of conditions of the
human visual system and shall include the examination for,
and adapting and fitting of, any and all kinds and types of
lenses including contact lenses.
(2) The administration and prescription of legend and
nonlegend drugs as approved by the Secretary of Health as
provided in section 4.3 for treatment of the [anterior
segment of the] eye, the eyelids, the lacrimal system and the
conjunctiva and the removal of superficial foreign bodies
from the ocular surface and adnexa so long as treatment of
diseases or conditions of the visual system, other than
glaucoma, as authorized under this paragraph shall not
continue beyond six weeks from the initiation of treatment
unless the prescribing optometrist documents consultation
with a licensed physician. As used in this paragraph, the
initiation of treatment may, but need not, include the
prescription or administration of pharmaceutical agents for
therapeutic purposes.
(3) The term shall not include:
(i) surgery, including, but not limited to, laser
surgery; the use of lasers for therapeutic purposes; and
the use of injections in the treatment of ocular disease;
(ii) the use of Schedule I and Schedule II
controlled substances;
[(iii) the use of beta blockers and the use of
steroids;
(iv) treatment of systemic disease; and
(v) the treatment of glaucoma.]
(iii) treatment of systemic disease; and
(iv) the treatment of glaucoma, except that
optometrists may use all topical pharmaceutical agents in
the treatment of primary open angle glaucoma, exfoliation
glaucoma and pigmentary glaucoma.
* * *
Section 2. The act is amended by adding sections to read:
Section 4.2. Additional requirements to prescribe and
administer pharmaceutical agents for the
treatment of certain types of glaucoma.
(a) Prior to treating glaucoma for the first time, all
therapeutically certified optometrists must have passed an
examination that included prescription and administration of
pharmaceutical agents for therapeutic purposes as required in
section 4.1(a). Therapeutically certified optometrists who
passed the examination under section 4.1(a)(2) shall also
complete at least 18 hours of continuing education in glaucoma.
In order to continue treating glaucoma, the therapeutically
certified optometrist shall, as part of the continuing education
required for renewal of a license under this act, complete at
least four hours in the study of the prescription and
administration of pharmaceutical agents for the treatment of
glaucoma.
(b) Therapeutically certified optometrists who prescribe and
administer pharmaceutical agents for the treatment of glaucoma
permitted under this act shall obtain and maintain professional
liability insurance in accordance with section 3(a)(2.5), except
that the amount of professional liability insurance maintained
shall be a minimum of $1,000,000 per occurrence and $3,000,000
per annual aggregate.
Section 4.3. Approval of drugs.
Drugs shall be approved as follows:
(1) All drugs currently approved by the Secretary of
Health and in use in the practice of optometry on the
effective date of this section shall be deemed approved under
this section.
(2) Within 90 days of the effective date of this
section, the board shall submit a list of drugs authorized
under this act to the Secretary of Health, who, in
consultation with the Physician General, shall approve or
disapprove for good cause each drug. Upon failure of the
Secretary of Health to act within 90 days of receipt of the
list of drugs, the drugs shall be deemed approved for use
under this act.
(3) The State Board of Optometry shall provide the
Secretary of Health with lists of additional drugs for use
under this act after such drugs are approved by the Food and
Drug Administration, as published in the Code of Federal
Regulations. The Secretary of Health, in consultation with
the Physician General, shall approve or disapprove for good
cause any such drug within 90 days of the receipt of the
list. Upon failure of the Secretary of Health to act within
90 days, the drugs shall be deemed approved for use under
this act.
Section 3. Section 8(a) of the act is amended by adding a
paragraph to read:
Section 8. Violations and penalties.
(a) * * *
(3) It is unlawful for optometrists to hold themselves
out as performing laser surgery or using therapeutic lasers.
* * *
Section 4. This act shall take effect immediately.
APPROVED--The 16th day of December, A. D. 2002.
MARK S. SCHWEIKER
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