E2SHB 1291 -
By Conference Committee
Strike everything after the enacting clause and insert the following:
"NEW SECTION. Sec. 1 (1) The legislature finds that:
(a) Thousands of patients are injured each year in the United
States as a result of medical errors, and that a comprehensive approach
is needed to effectively reduce the incidence of medical errors in our
health care system. Implementation of proven patient safety strategies
can reduce medical errors, and thereby potentially reduce the need for
disciplinary actions against licensed health care professionals and
facilities, and the frequency and severity of medical malpractice
claims; and
(b) Health care providers, health care facilities, and health
carriers can and should be supported in their efforts to improve
patient safety and reduce medical errors by encouraging health care
facilities and providers to communicate openly with patients regarding
medical errors that have occurred and steps that can be taken to
prevent errors from occurring in the future, encouraging health care
facilities and providers to work cooperatively in their patient safety
efforts, and increasing funding available to implement proven patient
safety strategies.
(2) Through the adoption of this act, the legislature intends to
positively influence the safety and quality of care provided in
Washington state's health care system.
Sec. 2 RCW 5.64.010 and 1975-'76 2nd ex.s. c 56 s 3 are each
amended to read as follows:
(1) In any civil action against a health care provider for personal
injuries which is based upon alleged professional negligence ((and
which is against:)), or in any arbitration or mediation proceeding
related to such civil action, evidence of furnishing or offering or
promising to pay medical, hospital, or similar expenses occasioned by
an injury is not admissible ((
(1) A person licensed by this state to provide health care or
related services, including, but not limited to, a physician,
osteopathic physician, dentist, nurse, optometrist, podiatrist,
chiropractor, physical therapist, psychologist, pharmacist, optician,
physician's assistant, osteopathic physician's assistant, nurse
practitioner, or physician's trained mobile intensive care paramedic,
including, in the event such person is deceased, his estate or personal
representative;
(2) An employee or agent of a person described in subsection (1) of
this section, acting in the course and scope of his employment,
including, in the event such employee or agent is deceased, his estate
or personal representative; or
(3) An entity, whether or not incorporated, facility, or
institution employing one or more persons described in subsection (1)
of this section, including, but not limited to, a hospital, clinic,
health maintenance organization, or nursing home; or an officer,
director, employee, or agent thereof acting in the course and scope of
his employment, including, in the event such officer, director,
employee, or agent is deceased, his estate or personal
representative;to prove liability for the injury)).
(2)(a) In a civil action against a health care provider for
personal injuries that is based upon alleged professional negligence,
or in any arbitration or mediation proceeding related to such civil
action, a statement, affirmation, gesture, or conduct identified in (b)
of this subsection is inadmissible as evidence if:
(i) More than twenty days before commencement of trial it was
conveyed by a health care provider to the injured person, or to a
person specified in RCW 7.70.065(1); and
(ii) It relates to the discomfort, pain, suffering, injury, or
death of the injured person as the result of the alleged professional
negligence.
(b) (a) of this subsection applies to:
(i) Any statement, affirmation, gesture, or conduct expressing
apology, fault, sympathy, commiseration, condolence, compassion, or a
general sense of benevolence; or
(ii) Any statement or affirmation regarding remedial actions that
may be taken to address the act or omission that is the basis for the
allegation of negligence.
Sec. 3 RCW 4.24.260 and 1994 sp.s. c 9 s 701 are each amended to
read as follows:
((Physicians licensed under chapter 18.71 RCW, dentists licensed
under chapter 18.32 RCW, and pharmacists licensed under chapter 18.64
RCW)) Any member of a health profession listed under RCW 18.130.040
who, in good faith, makes a report, files charges, or presents evidence
against another member of ((their)) a health profession based on the
claimed ((incompetency or gross misconduct)) unprofessional conduct as
provided in RCW 18.130.180 or inability to practice with reasonable
skill and safety to consumers by reason of any physical or mental
condition as provided in RCW 18.130.170 of such person before the
((medical quality assurance commission established under chapter 18.71
RCW, in a proceeding under chapter 18.32 RCW, or to the board of
pharmacy under RCW 18.64.160)) agency, board, or commission responsible
for disciplinary activities for the person's profession under chapter
18.130 RCW, shall be immune from civil action for damages arising out
of such activities. A person prevailing upon the good faith defense
provided for in this section is entitled to recover expenses and
reasonable attorneys' fees incurred in establishing the defense.
Sec. 4 RCW 18.130.160 and 2001 c 195 s 1 are each amended to read
as follows:
Upon a finding, after hearing, that a license holder or applicant
has committed unprofessional conduct or is unable to practice with
reasonable skill and safety due to a physical or mental condition, the
disciplining authority may consider the imposition of sanctions, taking
into account any prior findings of fact under RCW 18.130.110, any
stipulations to informal disposition under RCW 18.130.172, and any
action taken by other in-state or out-of-state disciplining
authorities, and issue an order providing for one or any combination of
the following:
(1) Revocation of the license;
(2) Suspension of the license for a fixed or indefinite term;
(3) Restriction or limitation of the practice;
(4) Requiring the satisfactory completion of a specific program of
remedial education or treatment;
(5) The monitoring of the practice by a supervisor approved by the
disciplining authority;
(6) Censure or reprimand;
(7) Compliance with conditions of probation for a designated period
of time;
(8) Payment of a fine for each violation of this chapter, not to
exceed five thousand dollars per violation. Funds received shall be
placed in the health professions account;
(9) Denial of the license request;
(10) Corrective action;
(11) Refund of fees billed to and collected from the consumer;
(12) A surrender of the practitioner's license in lieu of other
sanctions, which must be reported to the federal data bank.
Any of the actions under this section may be totally or partly
stayed by the disciplining authority. In determining what action is
appropriate, the disciplining authority must first consider what
sanctions are necessary to protect or compensate the public. Only
after such provisions have been made may the disciplining authority
consider and include in the order requirements designed to rehabilitate
the license holder or applicant. All costs associated with compliance
with orders issued under this section are the obligation of the license
holder or applicant.
The licensee or applicant may enter into a stipulated disposition
of charges that includes one or more of the sanctions of this section,
but only after a statement of charges has been issued and the licensee
has been afforded the opportunity for a hearing and has elected on the
record to forego such a hearing. The stipulation shall either contain
one or more specific findings of unprofessional conduct or inability to
practice, or a statement by the licensee acknowledging that evidence is
sufficient to justify one or more specified findings of unprofessional
conduct or inability to practice. The stipulation entered into
pursuant to this subsection shall be considered formal disciplinary
action for all purposes.
NEW SECTION. Sec. 5 The definitions in this section apply
throughout this chapter unless the context clearly requires otherwise.
(1) "Adverse event" means any of the following events or
occurrences:
(a) An unanticipated death or major permanent loss of function, not
related to the natural course of a patient's illness or underlying
condition;
(b) A patient suicide while the patient was under care in the
hospital;
(c) An infant abduction or discharge to the wrong family;
(d) Sexual assault or rape of a patient or staff member while in
the hospital;
(e) A hemolytic transfusion reaction involving administration of
blood or blood products having major blood group incompatibilities;
(f) Surgery performed on the wrong patient or wrong body part;
(g) A failure or major malfunction of a facility system such as the
heating, ventilation, fire alarm, fire sprinkler, electrical,
electronic information management, or water supply which affects any
patient diagnosis, treatment, or care service within the facility; or
(h) A fire which affects any patient diagnosis, treatment, or care
area of the facility.
The term does not include an incident.
(2) "Ambulatory surgical facility" means any distinct entity that
operates exclusively for the purpose of providing surgical services to
patients not requiring hospitalization, whether or not the facility is
certified under Title XVIII of the federal social security act.
(3) "Childbirth center" means a facility licensed under chapter
18.46 RCW.
(4) "Correctional medical facility" means a part or unit of a
correctional facility operated by the department of corrections under
chapter 72.10 RCW that provides medical services for lengths of stay in
excess of twenty-four hours to offenders.
(5) "Department" means the department of health.
(6) "Health care worker" means an employee, independent contractor,
licensee, or other individual who is directly involved in the delivery
of health services in a medical facility.
(7) "Hospital" means a facility licensed under chapter 70.41 RCW.
(8) "Incident" means an event, occurrence, or situation involving
the clinical care of a patient in a medical facility which:
(a) Results in unanticipated injury to a patient that is less
severe than death or major permanent loss of function and is not
related to the natural course of the patient's illness or underlying
condition; or
(b) Could have injured the patient but did not either cause an
unanticipated injury or require the delivery of additional health care
services to the patient.
The term does not include an adverse event.
(9) "Medical facility" means an ambulatory surgical facility,
childbirth center, hospital, psychiatric hospital, or correctional
medical facility.
(10) "Psychiatric hospital" means a hospital facility licensed as
a psychiatric hospital under chapter 71.12 RCW.
NEW SECTION. Sec. 6 (1) Each medical facility shall report to
the department the occurrence of any adverse event. The report must be
submitted to the department within forty-five days after occurrence of
the event has been confirmed.
(2) The report shall be filed in a format specified by the
department after consultation with medical facilities. It shall
identify the facility but shall not include any identifying information
for any of the health care professionals, facility employees, or
patients involved. This provision does not modify the duty of a
hospital to make a report to the department of health or a disciplinary
authority if a licensed practitioner has committed unprofessional
conduct as defined in RCW 18.130.180.
(3) Any medical facility or health care worker may report an
incident to the department. The report shall be filed in a format
specified by the department after consultation with medical facilities
and shall identify the facility but shall not include any identifying
information for any of the health care professionals, facility
employees, or patients involved. This provision does not modify the
duty of a hospital to make a report to the department of health or a
disciplinary authority if a licensed practitioner has committed
unprofessional conduct as defined in RCW 18.130.180.
(4) If, in the course of investigating a complaint received from an
employee of a licensed medical facility, the department determines that
the facility has not undertaken efforts to investigate the occurrence
of an adverse event, the department shall direct the facility to
undertake an investigation of the event. If a complaint related to a
potential adverse event involves care provided in an ambulatory
surgical facility, the department shall notify the facility and request
that they undertake an investigation of the event. The protections of
RCW 43.70.075 apply to complaints related to adverse events or
incidents that are submitted in good faith by employees of medical
facilities.
NEW SECTION. Sec. 7 The department shall:
(1) Receive reports of adverse events and incidents under section
6 of this act;
(2) Investigate adverse events;
(3) Establish a system for medical facilities and the health care
workers of a medical facility to report adverse events and incidents,
which shall be accessible twenty-four hours a day, seven days a week;
(4) Adopt rules as necessary to implement this act;
(5) Directly or by contract:
(a) Collect, analyze, and evaluate data regarding reports of
adverse events and incidents, including the identification of
performance indicators and patterns in frequency or severity at certain
medical facilities or in certain regions of the state;
(b) Develop recommendations for changes in health care practices
and procedures, which may be instituted for the purpose of reducing the
number and severity of adverse events and incidents;
(c) Directly advise reporting medical facilities of immediate
changes that can be instituted to reduce adverse events and incidents;
(d) Issue recommendations to medical facilities on a facility-specific or on a statewide basis regarding changes, trends, and
improvements in health care practices and procedures for the purpose of
reducing the number and severity of adverse events and incidents.
Prior to issuing recommendations, consideration shall be given to the
following factors: Expectation of improved quality care,
implementation feasibility, other relevant implementation practices,
and the cost impact to patients, payers, and medical facilities.
Statewide recommendations shall be issued to medical facilities on a
continuing basis and shall be published and posted on the department's
publicly accessible web site. The recommendations made to medical
facilities under this section shall not be considered mandatory for
licensure purposes unless they are adopted by the department as rules
pursuant to chapter 34.05 RCW; and
(e) Monitor implementation of reporting systems addressing adverse
events or their equivalent in other states and make recommendations to
the governor and the legislature as necessary for modifications to this
chapter to keep the system as nearly consistent as possible with
similar systems in other states;
(6) Report no later than January 1, 2007, and annually thereafter
to the governor and the legislature on the department's activities
under this act in the preceding year. The report shall include:
(a) The number of adverse events and incidents reported by medical
facilities on a geographical basis and their outcomes;
(b) The information derived from the data collected including any
recognized trends concerning patient safety; and
(c) Recommendations for statutory or regulatory changes that may
help improve patient safety in the state.
The annual report shall be made available for public inspection and
shall be posted on the department's web site;
(7) Conduct all activities under this section in a manner that
preserves the confidentiality of documents, materials, or information
made confidential by section 9 of this act.
NEW SECTION. Sec. 8 (1) Medical facilities licensed by the
department shall have in place policies to assure that, when
appropriate, information about unanticipated outcomes is provided to
patients or their families or any surrogate decision makers identified
pursuant to RCW 7.70.065. Notifications of unanticipated outcomes
under this section do not constitute an acknowledgment or admission of
liability, nor can the fact of notification or the content disclosed be
introduced as evidence in a civil action.
(2) Beginning January 1, 2006, the department shall, during the
survey of a licensed medical facility, ensure that the policy required
in subsection (1) of this section is in place.
NEW SECTION. Sec. 9 When a report of an adverse event or
incident under section 6 of this act is made by or through a
coordinated quality improvement program under RCW 43.70.510 or
70.41.200, or by a peer review committee under RCW 4.24.250,
information and documents, including complaints and incident reports,
created specifically for and collected and maintained by a quality
improvement committee for the purpose of preparing a report of an
adverse event or incident shall be subject to the confidentiality
protections of those laws and RCW 42.17.310(1)(hh).
Sec. 10 RCW 43.70.110 and 1993 sp.s. c 24 s 918 are each amended
to read as follows:
(1) The secretary shall charge fees to the licensee for obtaining
a license. After June 30, 1995, municipal corporations providing
emergency medical care and transportation services pursuant to chapter
18.73 RCW shall be exempt from such fees, provided that such other
emergency services shall only be charged for their pro rata share of
the cost of licensure and inspection, if appropriate. The secretary
may waive the fees when, in the discretion of the secretary, the fees
would not be in the best interest of public health and safety, or when
the fees would be to the financial disadvantage of the state.
(2) Except as provided in section 12 of this act, fees charged
shall be based on, but shall not exceed, the cost to the department for
the licensure of the activity or class of activities and may include
costs of necessary inspection.
(3) Department of health advisory committees may review fees
established by the secretary for licenses and comment upon the
appropriateness of the level of such fees.
Sec. 11 RCW 43.70.250 and 1996 c 191 s 1 are each amended to read
as follows:
It shall be the policy of the state of Washington that the cost of
each professional, occupational, or business licensing program be fully
borne by the members of that profession, occupation, or business. The
secretary shall from time to time establish the amount of all
application fees, license fees, registration fees, examination fees,
permit fees, renewal fees, and any other fee associated with licensing
or regulation of professions, occupations, or businesses administered
by the department. In fixing said fees, the secretary shall set the
fees for each program at a sufficient level to defray the costs of
administering that program and the patient safety fee established in
section 12 of this act. All such fees shall be fixed by rule adopted
by the secretary in accordance with the provisions of the
administrative procedure act, chapter 34.05 RCW.
NEW SECTION. Sec. 12 A new section is added to chapter 43.70 RCW
to read as follows:
(1) The secretary shall increase the licensing fee established
under RCW 43.70.110 by two dollars for the health care professionals
designated in subsection (2) of this section and by two dollars per
licensed bed for the health care facilities designated in subsection
(2) of this section. Proceeds of the patient safety fee must be
deposited into the patient safety account in section 16 of this act and
dedicated to patient safety and medical error reduction efforts that
have been proven to improve, or have a substantial likelihood of
improving the quality of care provided by health care professionals and
facilities.
(2) The health care professionals and facilities subject to the
patient safety fee are:
(a) The following health care professionals licensed under Title 18
RCW:
(i) Registered nurses and licensed practical nurses licensed under
chapter 18.79 RCW;
(ii) Chiropractors licensed under chapter 18.25 RCW;
(iii) Dentists licensed under chapter 18.32 RCW;
(iv) Midwives licensed under chapter 18.50 RCW;
(v) Naturopaths licensed under chapter 18.36A RCW;
(vi) Optometrists licensed under chapter 18.53 RCW;
(vii) Osteopathic physicians licensed under chapter 18.57 RCW;
(viii) Osteopathic physicians' assistants licensed under chapter
18.57A RCW;
(ix) Pharmacists and pharmacies licensed under chapter 18.64 RCW;
(x) Physicians licensed under chapter 18.71 RCW;
(xi) Physician assistants licensed under chapter 18.71A RCW;
(xii) Podiatrists licensed under chapter 18.22 RCW; and
(xiii) Psychologists licensed under chapter 18.83 RCW; and
(b) Hospitals licensed under chapter 70.41 RCW and psychiatric
hospitals licensed under chapter 71.12 RCW.
NEW SECTION. Sec. 13 A new section is added to chapter 7.70 RCW
to read as follows:
(1) One percent of all attorneys' fees received for representation
of claimants or defendants in actions brought under this chapter that
result in payment to a claimant shall be paid as a patient safety set
aside. Proceeds of the patient safety set aside will be distributed by
the department of health in the form of grants, loans, or other
appropriate arrangements to support strategies that have been proven to
reduce medical errors and enhance patient safety, or have a substantial
likelihood of reducing medical errors and enhancing patient safety, as
provided in section 12 of this act.
(2) A patient safety set aside shall be transmitted to the
secretary of the department of health by the attorney who receives fees
under subsection (1) of this section for deposit into the patient
safety account established in section 16 of this act.
(3) The Washington state supreme court may by rule adopt procedures
to implement this section.
NEW SECTION. Sec. 14 A new section is added to chapter 43.70 RCW
to read as follows:
(1)(a) Patient safety fee and set aside proceeds shall be
administered by the department, after seeking input from health care
providers engaged in direct patient care activities, health care
facilities, health care provider organizations, and other interested
parties. In developing criteria for the award of grants, loans, or
other appropriate arrangements under this section, the department shall
rely primarily upon evidence-based practices to improve patient safety
that have been identified and recommended by governmental and private
organizations, including, but not limited to:
(i) The federal agency for health care quality and research;
(ii) The institute of medicine of the national academy of sciences;
(iii) The joint commission on accreditation of health care
organizations; and
(iv) The national quality forum.
(b) The department shall award grants, loans, or other appropriate
arrangements for at least two strategies that are designed to meet the
goals and recommendations of the federal institute of medicine's
report, "Keeping Patients Safe: Transforming the Work Environment of
Nurses."
(2) Projects that have been proven to reduce medical errors and
enhance patient safety shall receive priority for funding over those
that are not proven, but have a substantial likelihood of reducing
medical errors and enhancing patient safety. All project proposals
must include specific performance and outcome measures by which to
evaluate the effectiveness of the project. Project proposals that do
not propose to use a proven patient safety strategy must include, in
addition to performance and outcome measures, a detailed description of
the anticipated outcomes of the project based upon any available
related research and the steps for achieving those outcomes.
(3) The department may use a portion of the patient safety fee
proceeds for the costs of administering the program.
NEW SECTION. Sec. 15 A new section is added to chapter 43.70 RCW
to read as follows:
The secretary may solicit and accept grants or other funds from
public and private sources to support patient safety and medical error
reduction efforts under this act. Any grants or funds received may be
used to enhance these activities as long as program standards
established by the secretary are followed.
NEW SECTION. Sec. 16 A new section is added to chapter 43.70 RCW
to read as follows:
The patient safety account is created in the state treasury. All
receipts from the fees and set asides created in sections 12 and 13 of
this act must be deposited into the account. Expenditures from the
account may be used only for the purposes of this act. Moneys in the
account may be spent only after appropriation.
NEW SECTION. Sec. 17 A new section is added to chapter 43.70 RCW
to read as follows:
By December 1, 2008, the department shall report the following
information to the governor and the health policy and fiscal committees
of the legislature:
(1) The amount of patient safety fees and set asides deposited to
date in the patient safety account;
(2) The criteria for distribution of grants, loans, or other
appropriate arrangements under this act; and
(3) A description of the medical error reduction and patient safety
grants and loans distributed to date, including the stated performance
measures, activities, timelines, and detailed information regarding
outcomes for each project.
Sec. 18 RCW 43.70.510 and 2004 c 145 s 2 are each amended to read
as follows:
(1)(a) Health care institutions and medical facilities, other than
hospitals, that are licensed by the department, professional societies
or organizations, health care service contractors, health maintenance
organizations, health carriers approved pursuant to chapter 48.43 RCW,
and any other person or entity providing health care coverage under
chapter 48.42 RCW that is subject to the jurisdiction and regulation of
any state agency or any subdivision thereof may maintain a coordinated
quality improvement program for the improvement of the quality of
health care services rendered to patients and the identification and
prevention of medical malpractice as set forth in RCW 70.41.200.
(b) All such programs shall comply with the requirements of RCW
70.41.200(1) (a), (c), (d), (e), (f), (g), and (h) as modified to
reflect the structural organization of the institution, facility,
professional societies or organizations, health care service
contractors, health maintenance organizations, health carriers, or any
other person or entity providing health care coverage under chapter
48.42 RCW that is subject to the jurisdiction and regulation of any
state agency or any subdivision thereof, unless an alternative quality
improvement program substantially equivalent to RCW 70.41.200(1)(a) is
developed. All such programs, whether complying with the requirement
set forth in RCW 70.41.200(1)(a) or in the form of an alternative
program, must be approved by the department before the discovery
limitations provided in subsections (3) and (4) of this section and the
exemption under RCW 42.17.310(1)(hh) and subsection (5) of this section
shall apply. In reviewing plans submitted by licensed entities that
are associated with physicians' offices, the department shall ensure
that the exemption under RCW 42.17.310(1)(hh) and the discovery
limitations of this section are applied only to information and
documents related specifically to quality improvement activities
undertaken by the licensed entity.
(2) Health care provider groups of five or more providers may
maintain a coordinated quality improvement program for the improvement
of the quality of health care services rendered to patients and the
identification and prevention of medical malpractice as set forth in
RCW 70.41.200. For purposes of this section, a health care provider
group may be a consortium of providers consisting of five or more
providers in total. All such programs shall comply with the
requirements of RCW 70.41.200(1) (a), (c), (d), (e), (f), (g), and (h)
as modified to reflect the structural organization of the health care
provider group. All such programs must be approved by the department
before the discovery limitations provided in subsections (3) and (4) of
this section and the exemption under RCW 42.17.310(1)(hh) and
subsection (5) of this section shall apply.
(3) Any person who, in substantial good faith, provides information
to further the purposes of the quality improvement and medical
malpractice prevention program or who, in substantial good faith,
participates on the quality improvement committee shall not be subject
to an action for civil damages or other relief as a result of such
activity. Any person or entity participating in a coordinated quality
improvement program that, in substantial good faith, shares information
or documents with one or more other programs, committees, or boards
under subsection (6) of this section is not subject to an action for
civil damages or other relief as a result of the activity or its
consequences. For the purposes of this section, sharing information is
presumed to be in substantial good faith. However, the presumption may
be rebutted upon a showing of clear, cogent, and convincing evidence
that the information shared was knowingly false or deliberately
misleading.
(4) Information and documents, including complaints and incident
reports, created specifically for, and collected, and maintained by a
quality improvement committee are not subject to discovery or
introduction into evidence in any civil action, and no person who was
in attendance at a meeting of such committee or who participated in the
creation, collection, or maintenance of information or documents
specifically for the committee shall be permitted or required to
testify in any civil action as to the content of such proceedings or
the documents and information prepared specifically for the committee.
This subsection does not preclude: (a) In any civil action, the
discovery of the identity of persons involved in the medical care that
is the basis of the civil action whose involvement was independent of
any quality improvement activity; (b) in any civil action, the
testimony of any person concerning the facts that form the basis for
the institution of such proceedings of which the person had personal
knowledge acquired independently of such proceedings; (c) in any civil
action by a health care provider regarding the restriction or
revocation of that individual's clinical or staff privileges,
introduction into evidence information collected and maintained by
quality improvement committees regarding such health care provider; (d)
in any civil action challenging the termination of a contract by a
state agency with any entity maintaining a coordinated quality
improvement program under this section if the termination was on the
basis of quality of care concerns, introduction into evidence of
information created, collected, or maintained by the quality
improvement committees of the subject entity, which may be under terms
of a protective order as specified by the court; (e) in any civil
action, disclosure of the fact that staff privileges were terminated or
restricted, including the specific restrictions imposed, if any and the
reasons for the restrictions; or (f) in any civil action, discovery and
introduction into evidence of the patient's medical records required by
rule of the department of health to be made regarding the care and
treatment received.
(5) Information and documents created specifically for, and
collected and maintained by a quality improvement committee are exempt
from disclosure under chapter 42.17 RCW.
(6) A coordinated quality improvement program may share information
and documents, including complaints and incident reports, created
specifically for, and collected and maintained by a quality improvement
committee or a peer review committee under RCW 4.24.250 with one or
more other coordinated quality improvement programs maintained in
accordance with this section or with RCW 70.41.200 or a peer review
committee under RCW 4.24.250, for the improvement of the quality of
health care services rendered to patients and the identification and
prevention of medical malpractice. The privacy protections of chapter
70.02 RCW and the federal health insurance portability and
accountability act of 1996 and its implementing regulations apply to
the sharing of individually identifiable patient information held by a
coordinated quality improvement program. Any rules necessary to
implement this section shall meet the requirements of applicable
federal and state privacy laws. Information and documents disclosed by
one coordinated quality improvement program to another coordinated
quality improvement program or a peer review committee under RCW
4.24.250 and any information and documents created or maintained as a
result of the sharing of information and documents shall not be subject
to the discovery process and confidentiality shall be respected as
required by subsection (4) of this section and RCW 4.24.250.
(7) The department of health shall adopt rules as are necessary to
implement this section.
NEW SECTION. Sec. 19 The legislature finds that prescription
drug errors occur because the pharmacist or nurse cannot read the
prescription from the physician or other provider with prescriptive
authority. The legislature further finds that legible prescriptions
can prevent these errors.
Sec. 20 RCW 69.41.010 and 2003 c 257 s 2 and 2003 c 140 s 11 are
each reenacted and amended to read as follows:
As used in this chapter, the following terms have the meanings
indicated unless the context clearly requires otherwise:
(1) "Administer" means the direct application of a legend drug
whether by injection, inhalation, ingestion, or any other means, to the
body of a patient or research subject by:
(a) A practitioner; or
(b) The patient or research subject at the direction of the
practitioner.
(2) "Community-based care settings" include: Community residential
programs for the developmentally disabled, certified by the department
of social and health services under chapter 71A.12 RCW; adult family
homes licensed under chapter 70.128 RCW; and boarding homes licensed
under chapter 18.20 RCW. Community-based care settings do not include
acute care or skilled nursing facilities.
(3) "Deliver" or "delivery" means the actual, constructive, or
attempted transfer from one person to another of a legend drug, whether
or not there is an agency relationship.
(4) "Department" means the department of health.
(5) "Dispense" means the interpretation of a prescription or order
for a legend drug and, pursuant to that prescription or order, the
proper selection, measuring, compounding, labeling, or packaging
necessary to prepare that prescription or order for delivery.
(6) "Dispenser" means a practitioner who dispenses.
(7) "Distribute" means to deliver other than by administering or
dispensing a legend drug.
(8) "Distributor" means a person who distributes.
(9) "Drug" means:
(a) Substances recognized as drugs in the official United States
pharmacopoeia, official homeopathic pharmacopoeia of the United States,
or official national formulary, or any supplement to any of them;
(b) Substances intended for use in the diagnosis, cure, mitigation,
treatment, or prevention of disease in man or animals;
(c) Substances (other than food, minerals or vitamins) intended to
affect the structure or any function of the body of man or animals; and
(d) Substances intended for use as a component of any article
specified in (a), (b), or (c) of this subsection. It does not include
devices or their components, parts, or accessories.
(10) "Electronic communication of prescription information" means
the communication of prescription information by computer, or the
transmission of an exact visual image of a prescription by facsimile,
or other electronic means for original prescription information or
prescription refill information for a legend drug between an authorized
practitioner and a pharmacy or the transfer of prescription information
for a legend drug from one pharmacy to another pharmacy.
(11) "In-home care settings" include an individual's place of
temporary and permanent residence, but does not include acute care or
skilled nursing facilities, and does not include community-based care
settings.
(12) "Legend drugs" means any drugs which are required by state law
or regulation of the state board of pharmacy to be dispensed on
prescription only or are restricted to use by practitioners only.
(13) "Legible prescription" means a prescription or medication
order issued by a practitioner that is capable of being read and
understood by the pharmacist filling the prescription or the nurse or
other practitioner implementing the medication order. A prescription
must be hand printed, typewritten, or electronically generated.
(14) "Medication assistance" means assistance rendered by a
nonpractitioner to an individual residing in a community-based care
setting or in-home care setting to facilitate the individual's self-administration of a legend drug or controlled substance. It includes
reminding or coaching the individual, handing the medication container
to the individual, opening the individual's medication container, using
an enabler, or placing the medication in the individual's hand, and
such other means of medication assistance as defined by rule adopted by
the department. A nonpractitioner may help in the preparation of
legend drugs or controlled substances for self-administration where a
practitioner has determined and communicated orally or by written
direction that such medication preparation assistance is necessary and
appropriate. Medication assistance shall not include assistance with
intravenous medications or injectable medications, except prefilled
insulin syringes.
(15) "Person" means individual, corporation, government or
governmental subdivision or agency, business trust, estate, trust,
partnership or association, or any other legal entity.
(16) "Practitioner" means:
(a) A physician under chapter 18.71 RCW, an osteopathic physician
or an osteopathic physician and surgeon under chapter 18.57 RCW, a
dentist under chapter 18.32 RCW, a podiatric physician and surgeon
under chapter 18.22 RCW, a veterinarian under chapter 18.92 RCW, a
registered nurse, advanced registered nurse practitioner, or licensed
practical nurse under chapter 18.79 RCW, an optometrist under chapter
18.53 RCW who is certified by the optometry board under RCW 18.53.010,
an osteopathic physician assistant under chapter 18.57A RCW, a
physician assistant under chapter 18.71A RCW, a naturopath licensed
under chapter 18.36A RCW, a pharmacist under chapter 18.64 RCW, or,
when acting under the required supervision of a dentist licensed under
chapter 18.32 RCW, a dental hygienist licensed under chapter 18.29 RCW;
(b) A pharmacy, hospital, or other institution licensed,
registered, or otherwise permitted to distribute, dispense, conduct
research with respect to, or to administer a legend drug in the course
of professional practice or research in this state; and
(c) A physician licensed to practice medicine and surgery or a
physician licensed to practice osteopathic medicine and surgery in any
state, or province of Canada, which shares a common border with the
state of Washington.
(17) "Secretary" means the secretary of health or the secretary's
designee.
NEW SECTION. Sec. 21 If any provision of this act or its
application to any person or circumstance is held invalid, the
remainder of the act or the application of the provision to other
persons or circumstances is not affected.
NEW SECTION. Sec. 22 Sections 5 through 9 of this act constitute
a new chapter in Title
NEW SECTION. Sec. 23 Section 12 of this act is necessary for the
immediate preservation of the public peace, health, or safety, or
support of the state government and its existing public institutions,
and takes effect July 1, 2005."
E2SHB 1291 -
By Conference Committee
On page 1, line 2 of the title, after "practices;" strike the remainder of the title and insert "amending RCW 5.64.010, 4.24.260, 18.130.160, 43.70.110, 43.70.250, and 43.70.510; reenacting and amending RCW 69.41.010; adding new sections to chapter 43.70 RCW; adding a new section to chapter 7.70 RCW; adding a new chapter to Title 70 RCW; creating new sections; providing an effective date; and declaring an emergency."