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DEFENSE CONSIDERATIONS IN CENTRALIZATION OF
MEDICAL INFORMATION MANAGEMENT FOR LITIGATION
By: Elizabeth B. Juliano, Carey J. Marousek, and James R. Fell
Introduction
A published report from a Fortune 500 company indicated that while 95% of their
cases eventually settled, the discovery process alone consumed approximately 80%
of total litigation expenditures. 1 In mass medical product or toxic
tort litigation a significant portion of such discovery can involve the evaluation
of medical information and documents. With some companies reporting a need to respond
to a recent 300-1000% increase in class action lawsuits, 2 a cost-effective
approach to medical information management is clearly an opportunity to control
these expenditures.
The defense of mass tort typically involves the concerted efforts of corporate,
insurance, and outside counsel. As many such torts proceed, the number of defendants
often grows to include multiple corporations, each potentially with its own insurer
and outside counsel. As a large number of parties become enmeshed in the overall
defense process a complicated communications matrix evolves. The effective management
of medical information is often at the center of the process.
Conventional Medical Discovery
Traditionally, each defense party named in a mass product liability or toxic tort
has undertaken independent acquisition, review, and analysis of plaintiff medical
records. This approach may be redundant and expensive in that a single set of records
will be acquired multiple times, with numerous individuals evaluating identical
documents. A great deal of time is invested by counsel and their assistants in gathering,
sorting, and reviewing data, as opposed to focusing their legal expertise on the
assessment of relevant information. In addition, varying interpretations of the
same medical records may result due to differing methodological approaches.
The disadvantages of these overlapping functions are also realized as lost opportunities
as a result of disseminated information, limited time available for strategic planning,
and spiraling aggregate expenditures for all defendants. Such a decentralized approach
to medical information management prohibits the creation of a common source of medicolegal
knowledge from which to analyze the plaintiff population and engage in ultimate
strategic planning for the legal defense.
Collaborative Solution
The solution to the aforementioned situation is to centralize the medical information
management (MIM) initiative through the formation of a cooperative effort among
the defense participants. All elements associated with medical information management
for a given mass tort can thus be efficiently administered by one agency, which
is mutually selected by the group. This partnering medical information management
agent serves as the informational adhesive among the medical defense constituents.
Using a central source for coordination of medical record acquisition, review, analysis,
and storage also serves to diminish overlapping activities performed by defense
parties. Counsel is then freed to focus on its core competencies, as opposed to
sorting and shuffling mountains of both relevant and irrelevant medical records.
Furthermore, medicolegal specialists, typically nurse legal assistants, employed
in the offices of defense counsel are released to directly focus their attention
on interpreting the information provided by the central MIM source, assessing it
against trial strategy, assisting in the discovery process, etc.
Centralization Advantages – The “6 C’s”
A centralized MIM effort results in efficiency, cost, time, and quality benefits
derived from economies of scale and certain learning curve advantages. The six (6)
“C’s” of these benefits include:
-
Cost Sharing. The argument for centralization of MIM functions in mass torts is
most compelling from the perspective of cost sharing. Case preparation expenses
are minimized as one central agency acquires and stores a single copy of the pertinent
medical records. This documentation can then be reviewed and analyzed by the central
site’s medicolegal professionals, avoiding expensive duplication and shipping fees
associated with transmission of thousands of pages of medical records among the
various defense parties.
The centralized MIM firm can coordinate the distribution of a single medical summary
on each plaintiff to all cost sharing parties, further ensuring that all counsel
are “reading from the same book.” The production of an objective and neutral summary
of plaintiff medical records, without interpretation or recommendation of litigation
strategies, allows all defendants to participate in the use of one uniform product.
- Consistency. A primary value in centralization of MIM is seen in the consistency
of each medical review and analysis. The need for the attorney to adapt to varying
products, approaches, and writing styles is eliminated. Counsel can quickly become
familiar with the format of the medical summary document thus optimizing defense
preparation time. For example, a standardized format allows counsel to rapidly digest
a plaintiff’s medical history, even while aboard an airplane en route to a deposition
or hearing.
- Communication. As litigation in a mass tort evolves, questions may arise regarding
findings contained within the medical analysis. Centralization of MIM facilitates
“one-stop” answers to these questions from a designated MIM case manager who can
quickly and accurately research the information required.
- Coordination. The indications for centralization of the medical summary function
are even more compelling in litigation which spans jurisdictions, because the caseload
is rarely evenly distributed. In the typical situation, dockets reflect periods
of intense activity, with occasional “all hands on deck” situations occurring in
which hiring of temporary workers, with varying backgrounds and case orientation,
may become necessary. During subsequent periodic lulls in the litigation, the law
firm or corporation may be burdened with excessive worker capacity that poses a
budgetary and administrative drain. In these cases, MIM centralization releases
the law firm from supervision of human resources and medical review workflow, so
that attorney attention can be directed toward higher level functions in the given
litigation.
- Computers/Information Technology. Efficient MIM for mass tort litigation requires
state-of-the-art information technology for rapid storage and retrieval of case
data. While the defense of mass torts entails clear and effective communication
among all parties, a frequently encountered barrier originates in the differing
computer systems and software programs from one legal department to another. Centralization
of MIM reduces or eliminates the impediments associated with varying computer packages
as one central agency oversees the development, implementation, and maintenance
of a database compatible with those systems of the attorney end-users.
- Continual Quality Assurance. A review of medical records which is free of date,
diagnosis, interpretation, and other errors is critical in defending any case. In
relying on a centralized agency for MIM, accountability and quality are guaranteed
as a system of Continual Quality Assurance (CQA) checks and balances should already
be part of the administrator’s workflow operation.
Functional Integration
Benefits of centralized MIM extend beyond the development of the medical record
review and analysis. These outcomes are realized in functions of:
- Literature Reviews. In some mass tort litigation, an extensive review of the medical,
epidemiological, and toxicological literature is required. It is economically and
logistically impractical for each defense legal department to retain professional
researchers to investigate, analyze, and abstract these publications. However, centralized
MIM enables the costs associated with this aspect of case preparation to be distributed
among all end-users. Specialists can conduct reviews on pertinent research as required
by the litigation and disseminate common literature abstracts to all participating
parties.
- Education and Development. Education of legal staff in the clinical aspects of the
litigation is also expedited via centralized MIM. A medicolegal training specialist
can create a universal medical reference manual for a given mass tort fostering
a universal language among the defense firms. Moreover, the training specialist
can assemble a common medical and scientific curriculum relevant to the given litigation,
which can then be presented to designated personnel in each law firm.
- Expert Witness Identification. The identification of appropriate consulting and
testifying physicians, scientists, epidemiologists, toxicologists, and other experts
can be expedited through centralized MIM, avoiding the need for each individual
law firm to research, locate, screen, correspond, and contract with these individuals.
For example, an individual defense firm may have had limited prior experience identifying
and selecting a suitable toxicologist with clinical expertise in the hazards of
industrial solvent exposure. However, given the day-to-day nature of its work in
the field, the central MIM agency will already have the resources in place to cost-effectively
ascertain the best consultant for this particular litigation.
- Medical Defense Newsletter. Protracted mass tort litigation can sometimes justify
the creation of a restricted-access medicolegal newsletter whose readership is limited
to the defense group membership. Content of this newsletter is tightly focused on
subject matter germane to the defense of the particular litigation, and can include
items such as abstracts of recently published scientific and medical research, membership
discussion regarding recent applicable court rulings, relevant book reviews, etc.
- Meetings. Medical defense strategy is enhanced by face-to-face communication among
defense group membership. To expedite this exchange, the medical information management
agency can coordinate and organize meetings at a common location, or alternatively
structure office videoconferencing.
Summary
The ultimate decision to centralize medical information management for litigation
must be founded on several factors. Ideally, the decision making process begins
early in the litigation so that maximum structure can be imposed on medical review
procedures and maximum cost advantages can be gained by avoiding duplicative efforts.
Proactive consultation is advised with a MIM specialist experienced in coordination,
project management, and review of voluminous medical records for multiple end-users.
Sager TL and Mayer DG. A New Era: The DuPont Legal System. EI du Pont de Nemours
and Company, 1997; 6.
Donohue TJ. America’s Legal System: Out of Control? Innocent Companies are Hammered.
Journal of Commerce. March 13, 1998; 7A.
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