HOUSE BILL REPORT
HB 2292
As Reported by House Committee On:
Judiciary
Title: An act relating to improving health care by increasing patient safety, reducing medical errors, reforming medical malpractice insurance, and resolving medical malpractice claims fairly without imposing mandatory limits on damage awards or fees.
Brief Description: Addressing health care liability reform.
Sponsors: Representatives Lantz, Cody, Campbell, Kirby, Flannigan, Williams, Linville, Springer, Clibborn, Wood, Fromhold, Morrell, Hunt, Moeller, Green, Kilmer, Conway, O'Brien, Sells, Kenney, Kessler, Chase, Upthegrove, Ormsby, Lovick, McCoy and Santos.
Brief History:
Judiciary: 3/22/05, 3/25/05 [DPS].
Brief Summary of Substitute Bill |
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HOUSE COMMITTEE ON JUDICIARY
Majority Report: The substitute bill be substituted therefor and the substitute bill do pass. Signed by 6 members: Representatives Lantz, Chair; Flannigan, Vice Chair; Williams, Vice Chair; Kirby, Springer and Wood.
Minority Report: Do not pass. Signed by 3 members: Representatives Priest, Ranking Minority Member; Rodne, Assistant Ranking Minority Member; and Serben.
Staff: Edie Adams (786-7180).
Background:
The Washington Constitution gives the people the power to legislate through the initiative
process, either by initiative directly to the people or by initiative to the Legislature. Under the
Constitution, the Legislature may deal with an initiative to the Legislature in one of the
following ways: (1) enact the initiative during the regular session; (2) reject the initiative or
take no action on it, in which case the measure is submitted to a vote of the people at the next
general election; or (3) reject or take no action on the measure and propose a different
measure dealing with the same subject, in which case both the initiative and the legislative
alternative are submitted to a vote of the people.
The people have submitted two initiatives to the Legislature, Initiatives 330 and 336, which
both deal broadly with the health care liability system. Initiative 330 proposes changes to the
civil liability system as applied to medical negligence cases. Initiative 336 proposes changes
to the medical malpractice insurance system, the health care system's handling of negligence
and unanticipated outcomes, and some aspects of the health care liability system.
INITIATIVE 330
Limitations on Non-Economic Damages: A $350,000 cap on a claimant's non-economic
damages award is established, regardless of the number of health care professionals or health
care institutions or entities involved. An additional $350,000 award for non-economic
damages is allowed against a health care institution that is liable for acts of persons other than
health care professionals, up to a maximum of $700,000 combined for all institutions.
If the limitation on non-economic damages is ruled unconstitutional, it will take effect after a
state constitutional amendment is passed that empowers the Legislature to place limits on
non-economic damages in civil actions or after passage of a federal law allowing such
limitations.
Attorneys' Contingency Fees: An attorney's contingency fee for handling a medical
negligence case is limited to no more than: 40 percent of the first $50,000 recovered; 33.33
percent of the next $50,000; 25 percent of the next $500,000; and 15 percent of any amount
in which the recovery exceeds $600,000. These limits apply to recoveries received in any
manner, including by judgment, settlement, or alternative dispute resolution.
Prior Notice and Mandatory Mediation: A plaintiff in a medical negligence action must
provide a defendant with 90-days prior notice of the intention to file a lawsuit. All medical
negligence actions are subject to mandatory mediation without exception, unless the action is
subject to binding arbitration.
Statute of Limitations: A medical negligence action must be commenced within the earlier
of three years from the act or omission, or one year from the time the patient discovered or
reasonably should have discovered that the injury was caused by the act or omission. An
action may be brought after the three-year statute of limitations period only under the
following circumstances:
Tolling of the statute of limitations for minority, incompetency, disability, or imprisonment is
eliminated.
Collateral Sources: Evidence of any collateral source payment made or to be made in the
future may be introduced into evidence. The party receiving the collateral payments may
present evidence of amounts paid to secure the right to the compensation. The ability of the
plaintiff to show an obligation to repay the collateral source payment is removed. Rights of
subrogation or reimbursement from a plaintiff's tort judgment are prohibited unless required
under superseding federal law.
Arbitration Clauses: A binding arbitration clause in a health care services contract must be
the first provision of the contract and must be expressed in language provided in the act. A
disclosure concerning binding arbitration must be provided in bold type immediately
preceding the signature line in the contract. A binding arbitration clause that complies with
these requirements is declared not to be a contract of adhesion, unconscionable or otherwise
improper.
Periodic Payment of Damages: An award of future economic and non-economic damages of
$50,000 or more must be paid by periodic payments at the request of any party. A judgment
debtor who is not adequately insured must post security adequate to satisfy the judgment.
The periodic payment judgment may be modified upon the death of the judgment creditor to
eliminate payments for future medical treatment, care or custody, loss of bodily function, or
pain and suffering. Money damages for loss of future earnings may not be reduced or
terminated upon the judgment creditor's death, but must be paid to persons to whom the
judgment creditor owed a duty of support.
If the debtor has a continuing pattern of failing to make payments, the court must find the
debtor in contempt of court and order the debtor to pay damages suffered as a result of the
failure to make timely payments, including court costs and attorneys' fees.
Ostensible Agency: A hospital is not vicariously liable for the negligence of a health care
provider who is granted privileges to provide care at the hospital unless the provider is an
agent or employee of the hospital and was acting within the course and scope of the
provider's agency or employment with the hospital. A health care provider is not vicariously
liable for the negligence of another provider unless the other provider is an actual agent or
employee acting under the provider's direct supervision and control.
Vulnerable Adults: In civil actions involving abuse, exploitation, or neglect of a vulnerable
adult being cared for in a facility or by a home health, hospice, or home care agency, the
ability of a prevailing plaintiff to recover reasonable attorneys' fees and expert costs is
removed.
Joint and Several Liability: Joint and several liability is eliminated in medical negligence
actions, and each defendant is responsible for only his or her proportionate share of the
damages, except where the defendants acted in concert or one party acted as the agent or
under the direct supervision and control of another party.
INITIATIVE 336
Malpractice Insurance Rate Notification: The Office of the Insurance Commissioner
(Commissioner) must notify the public of any medical malpractice insurance rate filing where
the rate change is less than 15 percent, and any consumer may request a public hearing on the
rate filing. The Commissioner must order a public hearing on a rate filing of 15 percent or
more. Rate filings are not effective until approved by the Commissioner after the public
hearing. If no public hearing was held on the rate filing, the filing is approved 45 days after
public notice.
Supplemental Malpractice Insurance Program: A supplemental malpractice insurance
program is established to provide excess liability coverage to health care facilities and
providers who either self-insure or purchase liability insurance in amounts equal to specified
retained limit requirements. The program will pay claims and related defense costs in excess
of the retained limits up to the policy limits of the program. The program is operated by an
appointed board and is funded by annual premiums and potential capital calls.
Claims Reporting: Insuring entities and self-insurers must report monthly to the
Commissioner any medical malpractice claim that resulted in a final judgment, settlement, or
disposition with no indemnity payment. Facilities and providers must report the claim if the
insurer does not. Insurers who fail to report are subject to a fine of $250 per case up to a
maximum of $10,000. Facilities and providers who fail to report are subject to a fine or
disciplinary action by the Department of Health (Department).
The Commissioner must use the data to prepare aggregate statistical summaries and an
annual report summarizing and analyzing the data for trends in the types, frequency, and
severity of claims and the status of the medical malpractice market.
Health Care Provider Discipline: The Department must investigate a health care professional
who has three paid claims within the most recent five-year period where the indemnity
payment for each claim was $50,000 or more.
A person who has committed three incidents of medical malpractice, found through final
court judgments, can't be licensed or continue to be licensed to practice medicine. Mitigating
circumstances may be found where there is a strong potential for rehabilitation or for
remedial education or training that will prevent future harm to the public.
Medical Quality Assurance Commission (MQAC): The public membership component of
the MQAC is increased from four to six members, and at least two of the public members
must be representatives of patient advocacy groups.
Patient Disclosure: A health care provider's failure to disclose the provider's experience with
a treatment at the patient's request is a violation of the duty to secure informed consent.
Upon written request of a patient or immediate family member of a disabled or deceased
patient, a health care facility or provider must make available for examination and copying
any records made or received by the facility or provider relating to any adverse medical
incident. The identity of a patient and any information protected by privacy restrictions under
federal law may not be disclosed in providing the access. "Adverse incident" means
negligence, intentional misconduct, and any other act or omission that caused or could have
caused injury or death to a patient.
Court Reports of Settlements or Verdicts: The court clerk must report to the Department any
medical malpractice action verdict or settlement that exceeds $100,000.
Expert Limits: In a medical malpractice action, each side is entitled to only two experts on
an issue except on a showing of necessity. If there are multiple parties on a side who are
unable to agree on the experts, the court may allow additional experts on an issue to be called
upon a showing of necessity.
Attorney Certification and Certificate of Merit: An attorney who files an action,
counterclaim, cross claim, or a defense certifies by his or her signature and filing that, to the
best of the attorney's knowledge and belief formed after reasonable inquiry, it is not frivolous.
A violation is punishable by sanctions, which may include costs and reasonable attorneys'
fees incurred by the other party in response to the frivolous claim, counterclaim, cross claim,
or defense.
Within 120 days after filing suit, an attorney or plaintiff must file a certificate of merit that
states that a qualified expert has been consulted and the expert believes that it is more
probable than not that the claim satisfies a basis for recovery.
Summary of Substitute Bill:
The Legislature finds that addressing the issues of consumer access to health care and the
increasing costs of medical malpractice insurance requires comprehensive solutions that
encourage patient safety, increase oversight of medical malpractice insurance, and make the
civil justice system more understandable, fair, and efficient. The Legislature finds that
neither Initiative 330 nor Initiative 336 offer the necessary comprehensive solution to these
problems.
The Legislature proposes this act as an alternative to both Initiatives 330 and 336. The act
contains a variety of changes designated under the following headings: Patient Safety,
Insurance Industry Reform, and Health Care Liability Reform.
PATIENT SAFETY
Statements of Apology: In a medical negligence action, a statement of fault, apology, or
sympathy, or a statement of remedial actions that may be taken, is not admissible as evidence
if the statement was conveyed by a health care provider to the injured person or certain family
members more than 20 days before the suit was filed and it relates to the person's discomfort,
pain, or injury.
Reports of Unprofessional Conduct: A health care professional who makes a good faith
report, files charges, or presents evidence to a disciplining authority against another member
of a health profession relating to unprofessional conduct or inability to practice safely due to
a physical or mental condition is immune in a civil action for damages resulting from such
good faith activities. A health care professional who prevails in a civil action on the good
faith defense is entitled to recover expenses and reasonable attorneys' fees incurred in
establishing the defense.
Medical Quality Assurance Commission: The public membership component of the MQAC
is increased from four to six members, and at least two of the public members must be
representatives of patient advocacy groups.
Health Care Provider Discipline: When imposing a sanction, a health profession disciplining
authority may consider prior findings of unprofessional conduct, stipulations to informal
disposition, and the actions of other Washington or out-of-state disciplining authorities.
Any combination of three unrelated orders for the following acts of unprofessional conduct
within a 10-year period results in the permanent revocation of a health care professional's
license:
A one-time finding of specified mitigating circumstances may be issued to excuse a violation
if there is either strong potential for rehabilitation or strong potential that remedial education
and training will prevent future harm to the public. A finding of mitigating circumstances
may be issued as many times as the disciplining authority determines that the act at issue
involved a high-risk procedure without any lower-risk alternatives, the patient was aware of
the procedure's risks, and the health care provider took remedial steps prior to the disciplinary
action.
Burden of Proof for License Suspension or Revocation: A new standard of proof of
"substantial and significant evidence" applies to the suspension or revocation of a physician's
license or a physician's assistant's license. This standard is higher than a preponderance of
the evidence and lower than clear and convincing evidence.
Disclosure of Adverse Events: A medical facility must report the occurrence of an "adverse
event" to the Department within 45 days of its occurrence. A medical facility or health care
worker may report the occurrence of an "incident" to the Department. "Adverse events" are
defined as: unanticipated deaths or major permanent losses of function; patient suicides;
infant abductions or discharges to the wrong family; sexual assault or rape; transfusions with
major blood incompatibilities; surgery performed on the wrong patient or site; major facility
system malfunctions; or fires affecting patient care or treatment. An "incident" is defined as
an event involving clinical care that could have injured the patient or that resulted in an
unanticipated injury less severe than death or a major permanent loss of function.
Reports of adverse events and incidents must identify the facility, but may not identify any
health care professionals, employees, or patients involved in the event or incident. Medical
facilities must provide written notification to patients who may have been affected by the
adverse event.
The Department is responsible for investigating reports of adverse events and establishing a
system for medical facilities and health care workers to report adverse events and incidents.
In addition, the Department must evaluate the data to identify patterns of adverse events and
incidents and recommend ways to reduce adverse events and incidents and improve health
care practices and procedures.
Coordinated Quality Improvement Programs: The types of programs that may apply to the
Department to become coordinated quality improvement programs are expanded to include
consortiums of health care providers that consist of at least five health care providers.
Prescription Legibility: Prescriptions for legend drugs must either be hand-printed,
typewritten, or generated electronically.
Medical Malpractice Premium Assistance: The Department must develop a program to
provide business and occupation tax credits for physicians who serve uninsured, Medicare,
and Medicaid patients in a private practice or a reduced fee access program for the uninsured.
INSURANCE INDUSTRY REFORM
Medical Malpractice Closed Claim Reporting: Self-insurers and insuring entities that write
medical malpractice insurance are required to report any closed claim resulting in a judgment,
settlement, or no payment to the Commissioner within 60 days after the claim is closed. The
reports must contain specified data relating to: the type of health care provider, specialty, and
facility involved; the dates when the event occurred, the claim was reported to the insurer,
and the suit was filed; the claimant's age and sex; and information about the settlement,
judgement, or other disposition of the claim, including an itemization of damages and
litigation expenses.
If an insuring entity or self-insurer does not report the claim to the Commissioner, the
provider or facility must report the claim to the Commissioner. The Commissioner may
impose a fine against insuring entities who fail to report of up to $250 per day up to a total of
$10,000. The Department may impose a fine against a facility or provider that fails to report
of up to $250 per day up to a total of $10,000.
A claimant or the claimant's attorney in a medical malpractice action must report to the
Commissioner the amount of court costs, attorneys' fees, or expert witness costs incurred in
the action.
The Commissioner must use the data to prepare aggregate statistical summaries of closed
claims and an annual report of closed claims and insurer financial reports. The annual report
must include specified information, such as: trends in frequency and severity of claims; an
itemization of economic and non-economic damages; an itemization of allocated loss
adjustment expenses; a loss ratio analysis; a profitability analysis for medical malpractice
insurers; a comparison of loss ratios and profitability; and a summary of approved medical
malpractice rate filings for the prior year, including analyzing the trend of losses compared to
prior years.
Any information in a closed claim report that may result in the identification of a claimant,
provider, health care facility, or self-insurer is exempt from public disclosure.
Underwriting Standards: Medical malpractice insurers must file their underwriting standards
at least 30 days before the standards become effective. The filing must identify and explain:
the class, type, and extent of coverage provided by the insurer; any changes that have
occurred to the underwriting standards; and how underwriting changes are expected to affect
future losses. The information is subject to public disclosure. "Underwrite" is defined as the
process of selecting, rejecting, or pricing a risk.
When an insurer takes an adverse action against an insured, such as cancellation of coverage
or an unfavorable change in coverage, the insurer may consider the following factors only in
combination with other substantive underwriting factors: (1) that an inquiry was made about
the nature or scope of coverage; (2) that a notification was made about a potential claim
which did not result in the filing of a claim; or (3) that a claim was closed without payment.
Cancellation or Non-Renewal of Liability Insurance Policies: The mandatory notice period
for cancellation or non-renewal of medical malpractice liability insurance policies is
increased from 45 days to 90 days. An insurer must actually deliver or mail to the insured a
written notice of cancellation of a medical malpractice liability insurance policy. For policies
the insurer will not renew, the notice must state that the insurer will not renew the policy
upon its expiration date.
Prior Approval of Medical Malpractice Insurance Rates: Medical malpractice rate filings and
form filings are changed from the current "use and file" system to a prior approval system.
An insurer must, prior to issuing a medical malpractice policy, file the policy rate and forms
with the Commissioner. The Commissioner must review the filing, which cannot become
effective until 30 days after its filing.
HEALTH CARE LIABILITY REFORM
Statutes of Limitations and Repose: Tolling of the statute of limitations during minority is
eliminated.
The eight-year statute of repose is re-established. Legislative intent and findings regarding
the justification for a statute of repose are provided in response to the Washington Supreme
Court's decision overturning the statute of repose in DeYoung v. Providence Medical Center.
Expert Witnesses: An expert witness in a medical malpractice action must meet the
following qualifications: (1) have expertise in the condition at issue in the action; and (2)
was engaged in active practice or teaching in the same or similar area of practice or specialty
as the defendant at the time of the incident, or at the time of retirement for a provider who
retired no more than five years prior to suit. The court may waive these requirements under
specified circumstances.
An expert opinion provided during the course of a medical malpractice action must be
corroborated by admissible evidence, such as treatment or practice protocols or guidelines,
objective academic research, or clinical trials.
The number of expert witnesses allowed in a medical negligence action is limited to two per
side on an issue, except upon a showing of good cause. If there are multiple parties on a side
and they are unable to agree on the experts, the court may allow additional experts for good
cause. All parties to a medical malpractice action must file a pretrial expert report that
discloses the identity of all expert witnesses and states the nature of the testimony the experts
will present at trial. Further depositions of the experts are prohibited. The testimony
presented by an expert at trial is limited in nature to the opinions presented in the pretrial
report.
Certificate of Merit: In medical negligence actions involving a claim of a breach of the
standard of care, the plaintiff must file a certificate of merit at the time of commencing the
action, or no later than 45 days after filing the action if the action is filed 45 days prior to the
running of the statute of limitations. The certificate of merit must be executed by a qualified
expert and state that there is a reasonable probability that the defendant's conduct did not
meet the required standard of care based on the information known at the time. The court for
good cause may grant up to a 90-day extension for filing the certificate of merit.
Failure to file a certificate of merit that complies with these requirements results in dismissal
of the case. If a case is dismissed for failure to comply with the certificate of merit
requirements, the filing of the claim may not be used against the health care provider in
liability insurance rate setting, personal credit history, or professional licensing or
credentialing.
Offers of Settlement: An offer of settlement provision is created for medical malpractice
actions. In an action where a party made an offer of settlement that is not accepted by the
opposing party, the court may, in its discretion, award prevailing party attorneys' fees.
"Prevailing party" means a party who makes an offer of settlement that is not accepted by the
opposing party and who improves his or her position at trial relative to his or her offer of
settlement.
In the case of a defendant, the offer of settlement provision applies only if the defendant
previously made a disclosure to the claimant within seven days of learning that the claimant
suffered an unanticipated outcome. The disclosure must have included: disclosure of the
unanticipated outcome; an apology or expression of sympathy; and assurances that steps
would be taken to prevent similar occurrences in the future.
When determining whether an award of attorneys' fees should be made to a prevailing party,
the court may consider: (1) whether the party who rejected the offer of settlement was
substantially justified in bringing the case to trial; (2) the extent to which additional relevant
and material facts became known after the offer was rejected; (3) whether the offer of
settlement was made in good faith; (4) the closeness of questions of fact and law at issue in
the case; (5) whether a party engaged in conduct that unreasonably delayed the proceedings;
(6) whether the circumstances make an award unjust; and (7) any other factor the court deems
appropriate.
Voluntary Arbitration: A new voluntary arbitration system is established for disputes
involving alleged professional negligence in the provision of health care. The voluntary
arbitration system may be used only where all parties have agreed to submit the dispute to
voluntary arbitration once the suit is filed, either through the initial complaint and answer, or
after the commencement of the suit upon stipulation by all parties.
The maximum award an arbitrator can make is limited to $1,000,000 for both economic and
non-economic damages. In addition, the arbitrator may not make an award of damages based
on the "ostensible agency" theory of vicarious liability.
The arbitrator is selected by agreement of the parties, and the parties may agree to more than
one arbitrator. If the parties are unable to agree to an arbitrator, the court must select an
arbitrator from names submitted by each side. A dispute submitted to the voluntary
arbitration system must follow specified time periods that will result in the commencement of
the arbitration no later than 10 months after the parties agreed to submit to voluntary
arbitration.
The number of experts allowed for each side is generally limited to two experts on the issue
of liability, two experts on the issue of damages, and one rebuttal expert. In addition, the
parties are generally entitled to only limited discovery. Depositions of parties and expert
witnesses are limited to four hours per deposition and the total number of additional
depositions of other witnesses is limited to five per side, for no more than two hours per
deposition.
There is no right to a trial de novo on an appeal of the arbitrator's decision. An appeal is
limited to the bases for appeal provided under the current arbitration statute for vacation of an
award under circumstances where there was corruption or misconduct, or for modification or
correction of an award to correct evident mistakes.
Collateral Sources: The collateral source payment statute is amended to remove the
restriction on presenting evidence of collateral source payments that come from insurance
purchased by the plaintiff. The plaintiff, however, may introduce evidence of amounts paid
to secure the right to the collateral source payments (e.g., premiums), in addition to
introducing evidence of an obligation to repay the collateral source compensation.
Frivolous Lawsuits: When signing and filing a claim, counterclaim, cross claim, or defense,
an attorney certifies that the claim or defense is not frivolous. An attorney who signs a filing
in violation of this section is subject to sanctions, including an order to pay reasonable
expenses and reasonable attorneys' fees incurred by the other party.
MISCELLANEOUS
The Secretary of State is directed to place this act on the ballot in conjunction with Initiative
330 and in conjunction with Initiative 336 at the next regular general election. A "concise
description" is designated for the ballot title. The concise description states that the
alternative would "improve health care by increasing patient safety, reducing medical errors,
reforming medical malpractice insurance, and resolving malpractice claims fairly."
Substitute Bill Compared to Original Bill:
The original bill did not contain the following provisions: (1) the creation of a new burden of
proof of "substantial and significant evidence" for the suspension or revocation of the license
of a physician or physician's assistant; (2) the Department of Health program to provide
business and occupation tax credits for physicians serving uninsured, Medicaid, or Medicare
patients; (3) the frivolous lawsuit section subjecting an attorney to sanctions for filing a
frivolous suit; and (4) the designation of a "concise description" of the alternative for the
ballot title.
With respect to statements of apology or fault made by a provider to an injured person, the
original bill allowed a statement of fault to be introduced into evidence under limited
circumstances for impeachment purposes. In addition, the original bill allowed the apology
or statement of fault to be made to a family member of the injured person only if the person
was incompetent.
With respect to closed claim reporting, the substitute bill made the following changes: (1)
extended the dates for commencement of reporting and for the Commissioner to issue the
statistical summaries and annual reports; (2) gave the Commissioner specific rule-making
authority to identify who has the primary obligation to report a claim when more than one
entity is providing coverage and to specify methodology for the reporting; and (3) clarified
when a facility or provider must report a claim when the insuring entity or self-insurer does
not.
With respect to expert witnesses, the substitute bill changed the limitation on the number of
experts to two per side (instead of two per party) and also changed references to "medical" in
the expert qualifications provision to references to "health profession" or "health care."
In addition, the substitute bill clarified that a disciplining authority's ability to consider prior
findings applies to findings of both in-state and out-of-state disciplining authorities.
Appropriation: None.
Fiscal Note: Requested on March 25, 2005.
Effective Date of Substitute Bill: The bill takes effect if approved by the people.
Testimony For: Both Initiatives 330 and 336 are flawed, and it is the Legislature's duty to
come up with an alternative that deals with patient safety, insurance reform, and tort reform.
The insurance market has improved and liability insurance is more affordable and accessible,
but you still need to makes changes to improve the system and help get through the future
hard markets. The alternative focuses on patient safety which provides a very positive focus.
The alternative also has the purpose of avoiding litigation and improving the insurance
industry. The public has been led to believe that rates are tied to an exploding tort system
when the reality is that the real problem is with insurance industry cycles.
The insurance reform contained in the alternative is important. The data reporting
component will help us evaluate what is happening in the market. Insurance companies
should submit their rates and policies to the Insurance Commissioner before they start using
them, and the 90-day cancellation requirement will provide more time for providers to find
replacement policies. The alternative should go farther and also address the issue of capacity
by establishing a supplemental malpractice insurance program similar to what is contained in
Initiative 336.
This alternative will make a real practical improvement to the system and will allow
resolution of disputes with less cost and without abolishing fundamental rights. It represents
reasonableness over extremism, patient safety over special interests, and the best interest of
people over political expediency. There is one small concern with eliminating expert
depositions. Depositions are a cost effective way to frame the issues and help cases get
resolved earlier.
(With concerns) It has become clear that the claims made a few years ago that an explosion in
lawsuits and payouts were causing the malpractice premium crisis are just not true. The
number of lawsuits when adjusted for population growth are down 15 percent in the last 10
years. Premiums are also down 7.7 percent, and Washington ranks 35th lowest in terms of
average premiums for physicians. It is important to focus on patient safety. Data show that
195,000 people a year die from medical errors. The cost of this is more than six times the
cost of the total medical malpractice liability system.
There are many good patient safety measures in the alternative, including adding two
consumer members to the Medical Quality Assurance Commission. However, we need to
make sure that complaints to that body are thoroughly investigated. In addition, the
alternative is missing the very important piece of public access to this information and
disclosure to individual patients. There should be language in the alternative prohibiting
confidentiality restrictions in settlements, as contained in Initiative 336. It is important that
this information be available to patients so they can make informed decisions about the
doctors they chose.
On the insurance side, the alternative is missing the important component of public
participation in insurance rate increases. Surplus lines carriers are concerned about being
included in the closed claim reporting requirement.
The establishment of expert qualifications and limitations on the number of experts and
expert depositions all interfere with the judges' ability to effectively manage trials and get to
the truth. These limitations may unnecessarily increase costs and protract litigation. The
expert qualifications should relate to the issue in the case rather than to the defendant's
particular practice and, as drafted, only allow physicians to be experts. The expert limits
should be two per side rather than allowing the stacking of multiple experts on one side.
There are also concerns with the statute of limitations running on minors.
The voluntary arbitration piece will provide a simpler, quicker, and less expensive way to
handle the majority of disputes. It will benefit doctors, hospitals, and claimants and should
take most of the cases out of the court system. The system should also include a reporting
mechanism for the arbitrator to report attorneys who file frivolous claims and doctors who
are found to have caused significant harm through their negligence.
The Washington Defense Trial Lawyers Association was reported to be involved in crafting
or reviewing this legislation, but this was not the case.
Testimony Against: Many physicians in this state are either leaving the state, leaving
practice, or significantly limiting their practice. Washington residents are suffering as a
result. Between 2000 and 2004, 14 percent of obstetrician-gynecologists stopped delivering
babies, and 39 percent of family practitioners stopped delivery babies. This represents a
combined 29 percent of physicians who have stopped delivering babies during that four-year
period.
After two years of trying to get meaningful reform adopted by the Legislature and after
significant frustrations, the medical association decided to pursue an initiative. Initiative 330
contains the key features for liability reform contained in the California MICRA law,
including a cap on non-economic damages, sliding scale cap on attorneys' fees, elimination of
the collateral source rule, periodic payment of future damages, and joint and several liability
reform.
Optimal reform must contain reasonable reform of the litigation system. The alternative does
not contain meaningful medical litigation reform. It represents a missed opportunity. The
voluntary arbitration provisions does nothing since voluntary arbitration is already a part of
the law. The alternative does not contain a cap on non-economic damages nor a sliding scale
cap on attorneys' fees. In addition, it does not contain joint and several liability reform,
elimination of the collateral source rule, or expansion of periodic payment of damages. All
of these features are necessary. The only successful approach is to enact meaningful liability
reform as contained in Initiative 330. A study of the California MICRA law found that law
does not reduce access to the court system as people have claimed.
The insurance industry has concerns with changing from a "use and file" to a prior approval
system. It is important for the industry to be able to develop products and introduce them in a
timely fashion in order to create and maintain a competitive marketplace. A prior approval
system is more appropriate for the less sophisticated segment of the insurance market.
Persons Testifying: (In support) Representative Lantz, prime sponsor; Senator Keiser;
Senator Kline; Mike Kreidler, Insurance Commissioner; Bill Daley, Washington Citizens
Action; and Mark Johnson and Ron Ward, Washington State Bar Association.
(With concerns) Martha Harden Cesar, Superior Court Judges' Association; Emilia Sweeney,
Washington Defense Trial Lawyers; Lauri Gearllach, Cheryl Marshall, Candi Taylor, and
Dolores Christiano, Citizens for Better Safer Healthcare; Larry Shannon and Joel
Cunningham, Washington State Trial Lawyers' Association; Will Parry, Puget Sound
Alliance for Retired Americans; and Tom Parker, Surplus Line Association.
(Opposed) Cliff Webster, Washington State Medical Association; Randy Revelle,
Washington State Hospital Association; Kris Tefft, Association of Washington Business; and
Mel Sorensen, Property Casualty Insurance Association.