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