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Pulling out all the stops in the LIS marketplace
May 2003 Eric Skjei
Thinking about upgrading or replacing your laboratory information
system? Take note: it’s not your father’s
LIS marketplace anymore.
Yes, it’s
a whole new market out there. New forces and factors range from
the need to accommodate genomics testing to the pressure to build
your outreach business, support Web-based order entry and results
reporting, handle multi-site operations, integrate robotics, and,
oh yes, manage your costs more closely than ever.
Once you go
shopping, you’ll find many good systems, all of which provide
the basics and more—but few of which can do it all. You’ll
find a marketplace dominated more and more by big players, one that
is steadily tilting in favor of integrated, single-source solutions
rather than interfaced, heterogeneous, best-of-breed systems. A
market in which, in this era of uncertain economics and turbulence,
virtually every vendor understands the importance of building strong
long-term relationships with clients.
Most vendors
agree that the LIS market is flat. New sales are, by and large,
replacement sales, sometimes prompted by the vendor’s decision
to sunset an older product.
“There
seems to have been a decline in new lab system buying over the past
year,” says Sidney Goldblatt, MD, lab director at Conemaugh
Health System, Johnstown, Pa., and former CEO of Sunquest, now Misys
Healthcare Systems. “It could be a cyclical phenomenon related
to the general austerity in the health care industry. But I think
it’s also sort of a breather in which clients are stepping
back and assessing their strategic direction.”
As recently
as 10 years ago, the person at the center of a search for a new
LIS probably would have been the laboratory manager. Today, that
assignment is at least as likely to fall to the chief information
officer. “Even from the LIS point of view, the sell is now
at least in part, if not in a very dominant way, to the CIO,”
says Bruce Friedman, MD, professor of pathology and director of
pathology data systems, University of Michigan Health System, Ann
Arbor.
This shift to
the primacy of the CIO favors large, unified solutions over best-of-breed
alternatives. With the CIO in charge, Dr. Friedman says, the upgrade
or purchase decision is less likely to be driven by functionality
than by enterprise-wide concerns for ease of integration among clinical
areas, notably radiology, pharmacy, and the lab, and possibly such
computer-intensive departments as radiation oncology and cardiology.
(Conformance with standards and consolidation along the lines of
locally favored hardware and operating systems also play a major
role in decisionmaking, Dr. Friedman says.)
Because best-of-breed
options typically imply interfacing rather than tight integration
for data exchange, and because interfacing can be an area of slow
or problematic data exchange, these options may be subjected to
greater scrutiny than ever before, even if they do offer superior
functionality. “One could argue that having to sell to the
CIO inhibits the best-of-breed approach for what is sometimes called
the ‘good-enough’ approach to the LIS purchase,”
Dr. Friedman says.
The good-enough
strategy is in many ways a “common denominator” approach,
Dr. Friedman adds. “The CIO wants to deal with a small number
of vendors, with large, established companies, and from a business
rather than a technology perspective, and this bias again favors
the larger organizations, like Siemens, McKesson, and Cerner,”
he says.
By contrast,
focusing on best-of-breed means focusing on functionality. And rightly
so, from the lab’s perspective, because a laboratory operating
within a health system is going to be held accountable for its financial
success and for how well it operates—and how well it operates
will be highly dependent on its IS tools. Moreover, best-of-breed
solutions are more likely to come from smaller, privately held vendors
who are often newer to the market—all traits guaranteed to
raise the CIO’s eyebrows.
“The CIO
is interested in a whole suite of products, in how well they interoperate,”
and in making sure they are from a dependable vendor, says Dr. Friedman.
The CIO is looking for “a vendor that is publicly traded,
on whom he or she can obtain financial information, and with whom
he or she can negotiate large, complex contracts.” In general,
the CIO will not dig deeply into the functionality and workflow
requirements of any given department as a primary consideration.
Dr. Goldblatt concurs. “Many institutions are now committed
to an integrated solution for all information technologies in their
clinical area, and they want to do it from a single vendor,”
he says. Admittedly, the success of HL7 is a mitigating factor in
this process. Virtually all systems have achieved a high level of
data integration through the use of HL7, and that level is improving
with the use of XML. Nonetheless, Dr. Goldblatt says, “many
institutions are increasingly anxious to harmonize all their clinical
data in a single vendor’s system.”
Dr. Friedman
cautions labs that favor the best-of-breed option against being
deprived of functionality that they consider essential to achieving
key operational and other performance goals because they will be
held responsible for those goals. “When all is said and done,
in aggressive organizations, the lab is still going to be assessed
on operating cost per test, among other measures,” says Dr.
Friedman. “And if you’re hobbled by a less-than-efficient
LIS, ultimately you’re going to be called to task.”
Blurred boundaries
One of the larger trends shaping the LIS market during the last
few years has been consolidation among providers and the related
formation of integrated delivery networks, or IDNs. This consolidation
has created what might be called a “hybridization” issue,
which laboratories continue to encounter.
LISs traditionally
have fallen into one of two categories: a hospital LIS, focused
on the patient, and a reference LIS, focused on the customer (more
likely to be the office-based physician than the patient) and the
specimen. Consolidation and the attendant formation of core labs
require some of both product areas.
“In the last five years or so, the line has blurred between what’s
occurring
in the commercial reference lab business and what’s happening
in hospitals,” says Al DeStefano, CEO of SIA. “As hospital
labs, for example, have moved into the outpatient business, they
have had to face a whole new set of issues.”
Outpatient billing
requirements, for instance, differ from inpatient charge capture.
Labs also find they must manage courier systems and produce reports
formatted in significantly different ways to meet new client expectations.
The results are mixed. “Systems designed to handle reference
labs and systems designed to handle hospital labs’ needs don’t
cross over into one another’s area very well,” DeStefano
says.
The core lab
concept that arose out of consolidation still serves hospitals,
but doing so in a multi-site facility or integrated delivery network
often means taking on much of the operational role of a reference
lab, DeStefano notes. “The multi-site issues are being handled,
so the lab can tell where specimens are coming from and can get
the results back to the correct facility, but problems remain,”
he says. Simply having to produce patient-centered cumulative reports
for an inpatient environment as well as client-centered reports
for the outpatient and outreach environments can be tricky. “Most
systems don’t do this particularly well,” he says. “They’re
either patient-oriented or specimen-oriented.”
Labs of all
sizes and types, whether they operate alone or in a multi-site system,
are often pressured to become more entrepreneurial and to generate
revenues that can help offset costs. That often means building an
outreach business.
This need has
been prominent long enough that most LISs can address it. “Almost
every LIS vendor now has a relatively strong outreach solution,”
says Hal Weiner, president of Weiner Consulting, “at least
from the perspective of recognizing that the enterprise handles
more than patient beds, that there is a need to market services
outside the institution.” At the
same time, Weiner adds, there is a relative dearth in the market
of total solutions that accommodate everything needed in the outreach
environment, what is in effect a reference lab within the walls
of a hospital-based enterprise.
In outreach,
the virtues of integration can be particularly striking. J.P. Fingado,
enterprise vice president for lab solutions at Cerner, says the
only ones who are going to win in the outreach marketplace are the
suppliers who can offer a single physician system that supports
all of the ancillaries in one place. “You’ve got to
be able to have a single physician desktop that has all the specialty
lab functionality for ordering and reporting, as well as specialty
radiology and pharmacy, so physicians can get their results all
at once,” Fingado says. What physicians do not want, he adds,
is to have to log on to one application for lab results, another
for radiology orders, and a third for pharmacy information. “That’s
not going to fly,” he says.
Even best-of-breed
vendors need to understand and accept this underlying business reality,
concurs Bill Blair, vice president of sales and marketing for SIA.
“The outreach business is after the ‘whole doc,’”
he says. A hospital lab must understand first, that the hospital
is competing hard for the physician’s business, and second,
that from the physician’s point of view, the lab is too closely
allied to radiology, pharmacy, and several other areas of the hospital
to allow it to fly solo. “The doc needs to be able to hit
one icon on the desktop and have all the ancillary services of that
delivery system available to him or her, rather than have to separately
log on to get access to the lab, then log off, log on to radiology,
and so on,” he says.
Bringing the lab online
Many labs need to make better use of the Internet to create a stronger
relationship with clients, says Dr. Goldblatt. This often can be
done without upgrading or replacing the LIS. Many new lab portal
vendors have rushed to serve this niche. In a sense, these third-party
products extend the life of an incumbent LIS, particularly by facilitating
online ordering and reporting and by offering better, less costly
ways of delivering reports.
“Would
the need to make better use of the Internet drive someone to replace
their lab system?” Dr. Goldblatt asks. “My guess is
no, because there are a number of vendors that offer a solution
in this area and because those solutions are adaptable to existing
lab systems.”
This new category
of LIS/lab portal vendor, Dr. Friedman says, is carving out a set
of functions that can be grouped under the general heading of customer
relationship management, or CRM. Developed in other business contexts,
CRM is intended to provide software tools that organize the interaction
between supplier and client and make the process more manageable
and efficient. In a lab environment, CRM focuses on handling and
presenting test results to customers—primarily private-office
physicians—for reference labs and within hospital systems,
via a Web
front end.
Dr. Friedman
speculates that the appearance of a group of vendors serving a largely
CRM function for the lab signals the beginning of a divergence between
the classic LIS and a newer form of “disaggregated,”
or decentralized, LIS. As this divergence unfolds, the classic LIS
will persist, representing as it does many decades invested in expertise
and talent, but it will steadily move into the background of the
enterprise’s operations. The classic LIS will become less
apparent to customers and more dedicated to such highly specialized
lab functions as specimen tracking, creation of phlebotomy drawing
lists, and quality control. “What’s going to be apparent
to the customer are these Web-based, order-entry, result-reporting
engines, the so-called lab portals,” he says.
The classic
LIS was designed around the work and information that flow through
a hospital or complex reference lab environment, Dr. Friedman says.
He refers to this as a centralized LIS, or C-LIS. The new, emerging
LIS, destined to parallel and coexist with the C-LIS, is the decentralized
LIS, or D-LIS, he says, the fundamental architecture of which is
Web-based. The D-LISs—the first wave of which are products
from the lab portal vendors—will be designed to handle data
generated by POC testing, home health care testing, home kit testing,
and even direct access testing and results reporting, he adds.
“Direct
access testing, where patients sign on to a Web site and order tests
for themselves and pay for them out of pocket, has been enabled
by the Web, which can push the order engine directly into patients’
homes,” says Dr. Friedman. “Going retail” like
this is one of the few ways in which labs have gained access to
a new market.
Grappling
with genomics
For larger teaching facilities, one of the hottest forces driving
upgrades to the LIS, as well as the purchase of new systems and
third-party products, is genomics testing. “A small but growing
number of labs are frustrated by the inability to integrate their
new genomics testing into the current lab system,” says Dr.
Goldblatt, “which after all was not designed for this kind
of data, and which in many instances takes a different form from
the existing array of lab tests.”
Because genomics
information is data-intensive, one area where LISs are likely to
prove deficient is the database. “As we move toward personalized
patient databases, where the human genome has been specifically
mapped to that patient,” says Weiner, “we’re going
to be monitoring and testing predispositions to particular disease
states and, from the pharmacy side, seeking to provide patient-specific
drugs and creating individualized drug regimens.” As they
move futher into this area, labs will need enormous databases. That’s
something legacy systems—as well as many newer LISs—were
not designed for and are not likely to be able to handle.
Managing genomics
information will also require developing standards for presenting
and sharing this data. “In many cases this data is really
pattern data, and the image may be the best way to view, store,
and share it,” Dr. Goldblatt says. Lab systems can’t
easily accommodate this type of data, and doing so will require
new subsystems, he adds.
Cerner’s
Fingado makes a strong case for the benefits of integration: “When
labs start to do molecular testing, they’re going to want
to tie that work into pharmacy data,” to refine drug treatment,
among other things, he points out. To meet this need, he says, Cerner
is building a complex “bioinformatics layer” tied closely
to the application layer in the Cerner system architecture and accessible
by pharmacy, radiology, and the laboratory.
Robotics
and relationships
In general, lab information system vendors are still working to
improve the automation capabilities of their LISs. “Most legacy
LISs did not have a good way to handle the automation process,”
Weiner says. Newer LISs, by contrast, integrate more of those capabilities,
especially in the area of specimen management and tracking.
“The products
that are currently out there are beginning to address this problem,”
says SIA’s DeStefano, “but I don’t think anyone
has really good answers yet.” DeStefano believes that labs
are just beginning to understand the need to automate, and that
the need has not yet been addressed effectively in the marketplace.
Automation poses
many challenges. “For example, most LISs don’t take
error messages directly from the instrument,” says DeStefano.
If your analyzer is running out of reagent, the LIS needs to understand
the alerts. Otherwise, he says, “here you are chugging along
automatically, the analyzer is facing 300 glucoses, and all of a
sudden it is running out of reagent.” Without automatic communication
between the analyzer and the LIS, time-consuming and costly human
intervention will be needed.
Another challenge
is the system’s ability to assign and track unique identification
numbers, particularly for specimens. As simple as this sounds, this
capability isn’t universally available, and when it is available,
it’s not well-integrated into basic LIS functionality. “Unless
your LIS has true unique, specific specimen ID capabilities, it
is very hard for the lab to smoothly and fully track where the specimen
and all daughter tubes came from and where they are at any point
in time,” says DeStefano. Being able to locate specimens can
make the difference between efficient and inefficient automation.
To underscore
the automation differences between European and U.S. labs, SIA’s
Blair recalls a conversation he had with a pathologist in Germany.
“When I asked him to describe the difference between a reference
lab in Germany and a lab in the United States, his response was:
‘Here in Germany we get the sample, test it, process it, and
send out the results. In the United States you make friends with
the specimen—you relabel it, sometimes more than once, you
handle it repeatedly, you move it around.’”
In many cases
labs and vendors, including instrument vendors, have been forced
to create what is, in effect, a mini-LIS to handle automation-related
functions that the primary LIS isn’t up to. But the results
are often less than ideal. “Unless the system’s basic
architecture is designed for unique specimen ID and related functions,”
Blair says, “solving automation challenges by adding a layer
on top of an architecture that does not support that capability
probably just makes the process more complicated.”
As new as automation
and many of the other forces shaping the LIS market are, in many
ways the dynamic between client and supplier is returning to that
of an earlier era, with an emphasis on trust and integrity.
“We’re
getting back into the integrity game,” Cerner’s Fingado
says. “People really want to do business with folks they trust
and with whom they are comfortable. They want to work with a supplier
who can understand their long-term strategy, who takes the time
to listen, and who can actually be there to deliver for them.”
Fingado
is reminded of the conditions that shaped the LIS market when, over
a decade ago, he was an executive with leading anatomic pathology
system vendor CoPath. “This is like it was when we started
to automate the AP business 12 years ago,” he says. And, he
adds, it’s something of a refreshing change from “the
race for functionality, the race for technology, and the hype of
the Internet.”
Eric Skjei is a writer in Stinson Beach, Calif.
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