ePrescribing finally "Mandated" While Alternatives to Tamper-Proof
Paper Determined
In our last issue, we observed that "when it rains,
it pours" in alerting you to the merger of RxHub and Surescripts,
and to the Drug Enforcement Agency (DEA) notice of proposed
rule-making on ePrescribing. Well, we hope you kept your
raincoat on because it hasn't let up. In this special issue,
we provide an update on ePrescribing "mandates" and alert you to
alternatives to the tamper-proof prescription pads required by the
Centers for Medicare and Medicaid Services (CMS).
Congress gives ePrescribing a
boost through "carrots and sticks"
The new Medicare Physician Fee
fix legislation, passed on July 15, gives ePrescribing yet another
big boost. As anticipated, a bill was signed into law that made
ePrescribing “mandatory” in Medicare Part D. As we reported in the
July 8 issue of HIT Perspectives, it wasn’t a mandate in the
way we think of the term but an incentive and penalty (“carrot and
stick”) that will encourage physicians to prescribe electronically.
This provision was tucked away
in Section 132 of the Medicare Improvements for Patients and
Providers Act of 2008. It gives non-institutional physicians (both
solo and group practices) a way to earn enhanced incentive payments
for ePrescribing in for Medicare patients, based on the framework
established through CMS’s existing Physician Quality Reporting
Initiative (PQRI).
The new ePrescribing
provision offers a sliding scale set of incentive bonus payments:
two percent to a “successful electronic prescriber” in 2009 and
2010; a one percent bonus in 2011 and 2012; and a 0.5 percent bonus
in 2013.
However, if an eligible professional is not a successful electronic
prescriber for the one-year reporting period, the fee schedule
amount for their services would be reduced
by 1 percent in 2012, 1.5 percent in 2013, and 2 percent in 2014 and
beyond. Those who write too few prescriptions (determined by a
formula) are exempt, as are hardship cases, which CMS will determine
on a case-by-case basis.
The bonus system kicks in on January 1, 2009.
This gives CMS and all of us very limited time to consider how
implementation might work.
To be sure, the legislative language is pretty
vague and the “devil will be in the details.” Some such details
were provided in a July 21 media conference call hosted by Mike
Leavitt, secretary, Health and Human Services, and Kerry Weems,
Acting Administrator, CMS. I was invited to participate in my role
as this newsletter’s editor-in-chief.
Here’s what we know—and can infer—so far:
·
A big
driver was the potential savings of this program. The Congressional
Budget Office (CBO) projected that ePrescribing and other
efficiencies in medical care could save $156 billion over five
years. We understand that it’s not easy to get the CBO to score a
program as saving costs but it's necessary to get legislation
passed.
·
It is unclear how the new bonus payment system will
dovetail with the existing PQRI program. PQRI currently includes a
“quality measure” for ePrescribing; however, Weems said that
ePrescribing incentive will be additive; that is, a physician could
get a total bonus of four percent (two for other PQRI and two for
ePrescribing).
·
The
impact to providers depends on the situation. One vendor did a
"back-of-the-envelope" calculation assuming 33% Medicare patients,
and came up with incremental revenue of $3,366. For the 2007 PQRI
program, which offered a 1.5% increase in payments, individual
physicians received an average incentive payment of $600 and groups
$4,750, according to Weems.
·
If CMS decides to use current PQRI procedures,
complexities can be anticipated. For example, CPT or HCPCS codes do
not exist for ePrescribing under the current PQRI program, so CMS
has specified temporary “G” codes for this purpose. If physicians
go for the new ePrescribing bonus, then there would be
administrative and training costs for their staff in implementing
this system.
For details of PQRI reporting as it currently stands,
go to the PQRI portion of the CMS web site at
http://www.cms.hhs.gov/PQRI/34_2007_PQRI_Educational_Resources.asp
and see also
http://www.cms.hhs.gov/PQRI/downloads/2008PQRIMeasureSpecifications123107.pdf?agree=yes&next=Accept
·
The new
statute does not define ePrescribing. This is important, as
it is the second threshold requirement, beyond
prescriber eligibility. For providers on the fence about buying an
ePrescribing system, this could make a huge difference about what
and why they buy and how much it costs. For those who have already
made the investment decision could be penalized by more prescriptive
requirements.
· From
a federal affairs stand-point, CMS could implement this through
regulation, as part of a final rule implementing the new physician
fee schedule, or through administrative guidance. An ETA would be
November. There will be a conference this fall (date TBD), in which
CMS will provide more information.
From a public policy stand-point, questions remain
about the impact. Will it increase ePrescribing adoption—and, in a
backdoor way, spur the adoption of HIT? We believe that it will
help drive uptake of both. Incentive payments are good, and—coupled
with improved return on investment (ROI)—they should be solid
motivators to get physicians to jump on board. In addition, many
payers have been waiting to see what the Federal government would be
doing in this regard so they could consider their own adoption
incentive programs. There's no excuse to wait any longer.
To be sure, never before has there been such an array
of programs and payments to help physicians adopt technologies that
should save both lives and money.
Relative to these "mandates," there is still a lot to
be sorted out quickly so we can meet the January 1, 2009, start
date. Stay tuned or call us or drop us an eMail to help your
organization figure out the impact of this provision on your lines
of business and strategic planning .
Industry comes up with alternatives to tamper-proof
prescription pads
The
pharmacy industry has stepped up once again, this time making
Medicaid prescriptions easier for physicians to write while still
being compliant with federal and state anti-fraud requirements.
They did so by finding alternatives to tamper-proof prescription
pads, which physicians will be required to use for Medicaid
prescriptions on October 1, 2008, unless they are ePrescribing,
phoning or faxing prescriptions.
While it might appear that the
tamper-proof pad requirement is good for ePrescribing because
ePrescribing is an acceptable alternative, it's really quite a
challenge. The reason is that every ePrescriber has a need for
printing prescriptions, medication lists, documentation or
instructions for the patient, so the ePrescribing system is linked
to a printer with one tray which generally has plain paper.
What’s happened is that, through
efforts spearheaded by the National Council for Prescription Drug
Programs (NCPDP), industry standards for copy, erasure/modification,
and counterfeit resistance have been clarified. Now, though
the law clearly specifies the term "prescription pad," CMS has
stated that computer-generated prescriptions that are printed on
special paper inserted into the printer may be used to achieve copy
resistance, but it is not a requirement.
While an improvement, this still
represents a challenge to the industry. The reason: even
though computer-generated prescriptions on special paper is allowed,
this would mean that ePrescribers must have printers that have both
plain paper and the expensive tamper-proof paper, something that is
logistically challenging. So, the industry has been working
with CMS and the agency clarified its rules yet again. Now EMR-
or ePrescribing-generated prescriptions may also be printed on plain
paper and be fully compliant with all three categories of the
tamper-resistant regulations provided they contain at least one
feature from each of the three categories detailed below.
There are two technologies that might be used. One
is a patented process that creates a void pantograph, which
incorporates a hidden security word or image into the background of
a computer-printed prescription. The image will show up when the
document is copied or scanned. Another is called micro printing,
which uses a strip of tiny type that can be read with a 5X
magnifying glass or loupe. The type appears to be smeared when
photocopied by most copying machines.
The
void pantograph will require a licensing fee, which will be borne by
the technology company and likely passed along to the client so, in
a market with price-sensitive customers, this is not likely to be
the most popular short-term arrangement.
The
alternative is
micro printing, the cost of which will be negligible, provided the
printer can accommodate the fine printing. We have been told that
HP was consulted and most newer printers can accommodate micro
printing. If they cannot, HP will provide software that can do
so.
We
applaud NCPDP’s initiative to wrestle with this issue and CMS's
flexibility. We all will benefit from making it easier for
physicians to be prevent fraudulent prescriptions while serving our
most vulnerable populations.
We
also hope that the Drug Enforcement Agency (DEA) takes note that,
working with the industry and remaining flexible, it is possible to
come up with secure, cost-neutral (or low-cost) solutions that
provide greater security. |