Senate retains grip on GPOs;
FTC probe underscores Fed’s role
For the past 18 months, the U.S. Senate has delved into the
business practices of group purchasing organizations. The examination has
brought several versions of codes of conduct and some more substantial changes
to a once freewheeling GPO business that still handles medical supply contracts
for nearly all U.S. hospitals and a significant portion of the estimated $190
billion in annual supply spending by those facilities.
Today, that lengthy probe, launched by the Senate Anti-Trust
Subcommittee in April 2002, is showing few signs of loosening its firm grip on
the GPO industry. In fact, according to Seth Bloom, senior counsel to the Senate
subcommittee and a close aide to Sen. Herb Kohl (D-WI), a powerful member of
that panel, the investigation is pressing ahead. Bloom recently told a group of
mostly national accounts executives from key suppliers and purchasing executives
representing GPOs and integrated delivery networks that the GPO issue "remains a
top priority for the subcommittee." His remarks came in Orlando, FL during the
closing session of the 9th annual IDN Summit and Expo sponsored by NCI, the
Florida-based consulting and networking firm.
On the very day that Bloom was delivering his recap in
Orlando, in a hearing room in the Nation’s Capitol the Federal Trade Commission
and the Justice Department took a break from their high-profile National Do Not
Call List dealings and conducted an airing of the much lower-profile GPO matter.
The hearing was ostensibly as part of a fact-finding mission spurred by a letter
from Sen. Mike DeWine (R-OH) that called for the FTC to help decide, said Bloom,
"whether the guidelines affecting GPOs should be revised to make them more
sensitive to competition." Several state attorneys general are also scrutinizing
the GPO issue.
On hand at the FTC hearing were representatives of small
medical device manufacturers from the Medical Device Manufacturers Association,
the DC-based group that has been a thorn in the side of the GPO industry even
before last April’s Senate hearings, along with representatives of the Health
Industry Group Purchasing Association along with a few GPO and supplier
executives. While the MDMA has categorized the proceedings as an investigation
of anticompetitive practices in the hospital supply market, others during the
three-hour session briefed the FTC panel on the GPO codes of conduct and updated
the agency on progress made in GPO reform.
For example, in a written statement, HIGPA discussed its GPO
Code of Conduct—which the group says promotes competition, eliminates potential
conflicts of interest and provides cost savings to providers. In addition, HIGPA
president and CEO Dr. Robert Betz detailed the importance of GPOs to providers
and furnished examples of hospitals and other provider organizations agreeing
with this belief. Specifically, his written testimony highlighted recent
reaction by California providers opposing state legislation which he said would
weaken the GPO business model, as well as testimony by hospital executives
outlined in a May 2003 Lewin Group report. Dr. Betz warned the FTC that the
ripple effect of restricting GPO contracting practices will ultimately affect
federal administered healthcare programs. In support of this prediction, Dr.
Betz highlighted a September 2002 Muse & Associates study stating, "Providers,
payers and ultimately, consumers will pay more for products and services
purchased through GPOs if their ability to negotiate on behalf of their
providers is curtailed by additional restrictions on the GPO contracting
processes."
In closing, Dr. Betz stated, "I urge the FTC to act with
caution and not weaken a crucial mechanism that promotes competition and helps
providers reduce their purchasing costs which allows them to commit more
financial resources to patient care."
HIGPA also made note of the fact that healthcare providers
were not invited to attend the hearing, adding that providers were also left as
bystanders during Senate hearings on April 30, 2002 and the July 16 of this
year.
The MDMA called for a revision of "Health Care Policy
Statement 7," federal policy intended to shield GPOs from antitrust enforcement
action so that they could reduce healthcare costs through volume purchasing of
hospital supplies. MDMA has argued that a revision was needed on the grounds
that "anticompetitive behavior by some large GPOs has resulted in disincentives
to competition in the marketplace, stifled innovation and failure to reduce
healthcare costs overall."
As did the Senate, the FTC hearing looked at core GPO issues
such as product bundling, lengthy manufacturer/GPO sole-source contracts, and
high hospital/GPO commitment contracts. GPO leaders insist that sole-source
contracts may be necessary in certain instances due to the changing nature of
many product marketplaces. Shifting variations in the number of players in a
given market and technological changes in the products themselves, they say, may
require use of sole-source contracts in an effort to aggregate buying power and
achieve what they feel are lowest price levels.
There is, however, some debate regarding the lowest reaches
of those price levels. Some point to experiences with the Canadian
pharmaceutical market, one that is said to be mirrored in its medical device and
supply market, which call into question the so-called "bottom" of prices in a
given U.S. segment.
Bloom, meanwhile, added a new slant to the long-standing GPO
issue. He said that some small GPOs, which he did not name, "are taking
advantage of the GPO codes of conduct and offering bundling and sole-source
deals on their own and this disturbs us. We don’t want GPOs to use the codes to
their advantage."
Responding to a question from the Orlando audience, Bloom
restated the Antitrust Subcommittee’s lack of interest in gutting the Safe
Harbor rules, which Congress granted to exempt GPOs from anti-kickback laws. "As
to Safe Harbor," Bloom said, "we say mend it, don’t end it." At the same time,
he cautioned that the Senate was not finished studying the administrative fee
matter. Said Bloom, "We don’t want the amount of ad fees to influence the
contracting decision."
HPN