Title 31, Chapter 12, Section 13
( 31-12-13)
(a) For purposes of this Code section, the term: (1) "Bloodborne pathogens" means pathogenic microorganisms that
are present in human blood and can cause disease in humans. These
pathogens include, but are not limited to, hepatitis B virus
(HBV), hepatitis C virus (HCV), and human immunodeficiency virus
(HIV). (2) "Engineered sharps injury protection" means either: (A) A physical attribute built into or used with a needle device
used for withdrawing body fluids, accessing a vein or artery, or
administering medications or other fluids, which effectively
reduces the risk of an exposure incident by a mechanism such as
barrier creation, blunting, encapsulation, withdrawal,
retraction, destruction, or other effective mechanisms; or (B) A physical attribute built into or used with any other type
of needle device or into a nonneedle sharp, which effectively
reduces the risk of an exposure incident. (3) "Exposure incident" means any sharps injury which may
reasonably have exposed the person so injured to another person's
blood or other material potentially containing bloodborne
pathogens. (4) "Front-line health care workers" means workers from a variety
of occupational classifications and departments, including, but
not limited to, registered professional nurses, nurse aids,
medical technicians, phlebotomists, and physicians. (5) "Needleless system" means a device that does not utilize
needles for: (A) The withdrawal of body fluids after initial venous or
arterial access is established; (B) The administration of medication or fluids; or (C) Any other procedure involving the potential for an exposure
incident. (6) "Public employee" means an employee of a county board of
health established in accordance with Chapter 3 of this title or
an employee of the state or an agency or authority of the state
employed in a public health care facility or other facility
providing health care related services, currently not subject to
the jurisdiction of the federal Occupational Safety and Health
Administration. (7) "Public employer" means each employer having any public
employee with occupational exposure to blood or other material
potentially containing bloodborne pathogens. (8) "Sharp" means any object used or encountered in a health care
setting that can be reasonably anticipated to penetrate the skin
or any other part of the body and to result in an exposure
incident, including, but not limited to, needle devices, scalpels,
lancets, broken glass, and broken capillary tubes, but does not
include prefilled syringes or other drugs or biologics prepackaged
with an administration system requiring federal Food and Drug
Administration approval for changes to packaging, labeling, or
product. (9) "Sharps injury" means any injury caused by a sharp, including,
but not limited to, cuts, abrasions, or needlesticks. (10) "Sharps injury log" means a written or electronic record
satisfying the requirements of paragraph (2) of subsection (c) of
this Code section. (b) The department shall, no later than January 1, 2001, adopt a
bloodborne pathogen standard governing occupational exposure of
public employees to blood and other potentially infectious
materials. The standard shall be at least as prescriptive as the
standard promulgated by the federal Occupational Safety and Health
Administration and shall include, but not be limited to, the
following: (1) A requirement that the most effective available needleless
systems and sharps with engineered sharps injury protection be
included as engineering and work practice controls in all
facilities employing public employees except in cases where: (A) None are available in the marketplace; or (B) An evaluation committee, established by the employer, at
least half the members of which are front-line health care
workers, determines by means of objective product evaluation
criteria that use of such devices will jeopardize patient or
employee safety with regard to a specific medical procedure; (2) A requirement that each public employer develop and implement
an effective written exposure control plan that includes, but is
not limited to, procedures for: (A) Identifying and selecting needleless systems and sharps with
engineered sharps injury protection through the evaluation
committee described in subparagraph (B) of paragraph (1) of this
subsection; and (B) Updating the written exposure control plan when necessary to
reflect progress in implementing needleless systems and sharps
with engineered sharps injury protection as determined by the
evaluation committee described in subparagraph (B) of paragraph
(1) of this subsection, but in no event less than once every
year; (3) A requirement that information concerning exposure incidents
be recorded in a sharps injury log, including, but not limited to: (A) Date and time of the exposure incident; (B) Type and brand of sharp involved in the exposure incident;
and (C) Description of the exposure incident which shall include:
(i) Job classification of the exposed employee; (ii) Department or work area where the exposure incident
occurred; (iii) The procedure that the exposed employee was performing
at the time of the incident; (iv) How the incident occurred; (v) The body part involved in the exposure incident; (vi) If the sharp had engineered sharps injury protection,
whether the protective mechanism was activated, and whether
the injury occurred before the protective mechanism was
activated, during activation of the mechanism, or after
activation of the mechanism, if applicable; (vii) If the sharp had no engineered sharps injury protection,
the injured employee's opinion as to whether and how such a
mechanism could have prevented the injury, as well as the
basis for the opinion; and (viii) The employee's opinion about whether any other
engineering, administrative, or work practice control could
have prevented the injury, as well as the basis for the
opinion; (4) Ensuring that all front-line health care workers are trained
on the use of all engineering controls before they are introduced
into the clinical setting; and (5) Establishing an evaluation committee, at least half the
members of which are front-line health care workers, to advise the
employer on the implementation of the requirements of this Code
section. Members of the committee shall be trained in the proper
method of utilizing product evaluation criteria prior to the
commencement of any product evaluation. (c) The department shall consider additional enactments as part of
the bloodborne pathogen standard to prevent sharps injuries or
bloodborne pathogen exposure incidents including, but not limited
to, training and educational requirements, measures to increase
vaccinations, strategic placement of sharps containers as close to
the work area as practical, and increased use of personal protective
equipment. (d) The department shall compile and maintain a list of existing
needleless systems and sharps with engineered sharps injury
protection, which shall be available to assist public employers in
complying with the requirements of the bloodborne pathogen standard
adopted pursuant to this Code section. The list may be developed
from existing sources of information, including, but not limited to,
the federal Food and Drug Administration, the federal Centers for
Disease Control and Prevention, the National Institute of
Occupational Safety and Health, and the United States Department of
Veterans Affairs. (e) A fund is established within the department into which moneys
may be appropriated to provide for research and development, as well
as product evaluations, of needleless systems and sharps with
engineered sharps injury protection. |