2016 -- H 7949 SUBSTITUTE A | |
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LC005383/SUB A | |
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STATE OF RHODE ISLAND | |
IN GENERAL ASSEMBLY | |
JANUARY SESSION, A.D. 2016 | |
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A N A C T | |
RELATING TO BUSINESSES AND PROFESSIONS - COLLABORATIVE PHARMACY | |
PRACTICE | |
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Introduced By: Representative Raymond H. Johnston | |
Date Introduced: March 16, 2016 | |
Referred To: House Health, Education & Welfare | |
It is enacted by the General Assembly as follows: | |
1 | SECTION 1. Sections 5-19.2-2 and 5-19.2-3 of the General Laws in Chapter 5-19.2 |
2 | entitled "Collaborative Pharmacy Practice" are hereby amended to read as follows: |
3 | 5-19.2-2. Definitions. -- (a) "Collaborative practice agreement" is a written and signed |
4 | agreement, entered into voluntarily, between a pharmacist, with advanced training and experience |
5 | relevant to the scope of collaborative practice, one or more licensed pharmacist(s), with advanced |
6 | training and experience relevant to the scope of collaborative practice and one or more physicians |
7 | that defines the collaborative pharmacy practice in which the pharmacist pharmacist(s) and |
8 | physician(s) propose to engage. Collaborative practice agreements shall be made in the best |
9 | interest of public health. |
10 | (b) "Collaborative practice committee" shall consist of six (6) individuals: three (3) |
11 | individuals to be appointed by the board of pharmacy from nominees provided by the Rhode |
12 | Island Pharmacists Association and three (3) individuals to be appointed by the board of medical |
13 | licensure and discipline from nominees provided by the Rhode Island Medical Society. The |
14 | collaborative practice committee shall advise the director on all issues pertinent to the regulation |
15 | of collaborative practice agreements. |
16 | (c) "Collaborative pharmacy practice" is that practice of pharmacy whereby a |
17 | pharmacist, with advanced training and experience relevant to the scope of collaborative practice |
18 | one or more licensed pharmacist(s), with advanced training and experience relevant to the scope |
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1 | of collaborative practice agrees to work in collaboration with one or more physicians for the |
2 | purpose of drug therapy management of patients, such management to be pursuant to a protocol |
3 | or protocols authorized by the physician(s) and subject to conditions and/or limitations as set |
4 | forth by the department. A health care professional who has prescribing privileges and is |
5 | employed by a collaborating physician may be in such an agreement. |
6 | (d) "Drug therapy management" means the review, in accordance with a collaborative |
7 | practice agreement, of drug therapy regimen or regimens of patients by a pharmacist one or more |
8 | licensed pharmacist(s) for the purpose of rendering advice to one or more physicians who are |
9 | party to the agreement, or their physician designees, regarding adjustment of initiating, adjusting, |
10 | monitoring, or discontinuing the regimen. Decisions involving drug therapy management shall be |
11 | made in the best interests of the patient. In accordance with a collaborative practice agreement, |
12 | drug therapy management may include: |
13 | (1) Modifying and managing Initiating, adjusting, monitoring, or discontinuing drug |
14 | therapy; |
15 | (2) Collecting and reviewing patient histories; |
16 | (3) Obtaining and checking vital signs, including pulse, height, weight, temperature, |
17 | blood pressure, and respiration; and |
18 | (4) Under the supervision of, or in direct consultation with a physician one or more |
19 | physician(s), ordering and evaluating the results of laboratory tests directly related to drug |
20 | therapy when performed in accordance with approved protocols applicable to the practice setting |
21 | and providing such evaluation does not include any diagnostic component. |
22 | (e) "Limited-function test" means those tests listed in the federal register under the |
23 | Clinical Laboratory Improvement Amendments of 1988 (CLIA) as waived tests. For the purposes |
24 | of this chapter, limited-function test shall include only the following: blood glucose, hemoglobin |
25 | Alc, cholesterol tests, and/or other tests that are classified as waived under CLIA and are |
26 | approved by the United States Food and Drug Administration for sale to the public without a |
27 | prescription in the form of an over-the-counter test kit. |
28 | (f) "Pharmacist with advanced training and experience relevant to the scope of |
29 | collaborative practice" means a licensed pharmacist in this state with post-graduate educational |
30 | training. Such training shall include, but not be limited to, residency training; board certification; |
31 | certification from an accredited professional organization educational institution; or any other |
32 | continuing education provider approved by the director of health relevant to the proposed scope |
33 | of the collaborative practice agreement. "Pharmacist with advanced training and experience |
34 | relevant to the scope of collaborative practice" means a licensed pharmacist in this state with a |
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1 | Bachelor of Science in Pharmacy and post-graduate educational training or a Doctor of Pharmacy |
2 | degree. Such training shall include, but not be limited to, residency training; board certification; |
3 | certification from an accredited professional organization educational institution; or any other |
4 | continuing education provider approved by the director of health relevant to the proposed scope |
5 | of the collaborative practice agreement. |
6 | (g) "Practice of pharmacy" means the interpretation, evaluation, and implementation of |
7 | medical orders, including the performance of clinical laboratory tests, provided such testing is |
8 | limited to limited function tests as defined herein; the dispensing of prescription drug orders; |
9 | participation in drug and device selection; drug regiment reviews and drug or drug-related |
10 | research; provision of patient counseling and the provision of those acts or services necessary to |
11 | provide pharmaceutical care; drug therapy management pursuant to a collaborative practice |
12 | agreement; and the responsibility for the supervision for compounding and labeling of drugs and |
13 | devices (except labeling by a manufacturer, repackager, or distributor of nonprescription drugs |
14 | and commercially packaged legend drugs and devices); proper and safe storage of drugs and |
15 | devices; and maintenance of proper records for them. |
16 | 5-19.2-3. Collaborative pharmacy practice. -- (a) A pharmacist may engage in |
17 | collaborative pharmacy practice pursuant to a collaborative practice agreement in accordance |
18 | with provisions of this chapter or other applicable sections of the regulations. Any pharmacist or |
19 | physician desiring to engage in collaborate pharmacy practice shall execute a collaborative |
20 | practice agreement in accordance with regulations promulgated by the department. Each |
21 | collaborative practice agreement shall set forth at least the following: (1) site and setting where |
22 | the collaborative practice is to take place; (2) informed consent procedures; (3) qualifications of |
23 | participating pharmacist pharmacists and physicians; (4) the role of any employed health care |
24 | professional with prescriptive privileges participating in the collaborative practice; (5) scope of |
25 | conditions or diseases to be managed; (6) practice protocols; (7) risk management activities; and |
26 | (8) outcomes measurements. Each collaborative practice agreement shall be subject to review and |
27 | renewal on an annual a biennial basis. |
28 | (b) Any pharmacist or physician who deviates from or practices in a manner inconsistent |
29 | with the terms of a collaborative practice agreement shall be in violation of this chapter; such |
30 | shall constitute grounds for disciplinary action pursuant to this chapter. There shall be no civil |
31 | liability on the part of, or cause of action of any nature against, a physician or physician's agents |
32 | or employees for participation in collaborative pharmacy practice as the result of negligence or |
33 | fault on the part of the pharmacist participating in such collaborative practice agreement. |
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1 | SECTION 2. This act shall take effect upon passage. |
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LC005383/SUB A | |
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EXPLANATION | |
BY THE LEGISLATIVE COUNCIL | |
OF | |
A N A C T | |
RELATING TO BUSINESSES AND PROFESSIONS - COLLABORATIVE PHARMACY | |
PRACTICE | |
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1 | This act would redefine the type of advanced training and experience that is needed for |
2 | pharmacists to engage in collaborative practice and provides for biennial review of collaborative |
3 | practice agreements. |
4 | This act would take effect upon passage. |
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LC005383/SUB A | |
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