Implementing A Reprocessing Program:
Success Hinges on Planning
By Deborah Haley, RN, CNOR, MBA
Few headlines regarding the healthcare industry today offer good news, it
seems. Across the country, hospitals are struggling to deal with dwindling
reimbursements, budget shortfalls and the nursing shortage. Finding programs
that will deliver maximum savings to a facility's bottom line is more important
than ever.
Medical device reprocessing is helping to meet that need. Each year, the
healthcare industry discards millions of dollars in otherwise functional medical
devices after a single use. Reprocessing offers a safe, scientific alternative
that can help medical facilities realize as much as a 50 percent savings over
the purchase price of new medical devices without affecting the quality of
patient care.
In late 2000, new regulations by the Food and Drug Administration (FDA)
forced drastic changes for hospitals that reprocess single-use medical devices
in-house. The FDA guidance calls for hospitals and third-party reprocessors to
adhere to the same premarket submission requirements as device manufacturers.
For every device a facility wants to reprocess, it now must demonstrate the
safety and effectiveness of that device.
Since then, hospitals have had to decide whether to continue in-house
reprocessing of devices labeled for a single use (SUDs). Most have concluded
that they lack the resources to meet the premarket requirements and have begun
outsourcing to third-party companies to safely reprocess their SUDs.1
As a result, the reprocessing industry is experiencing significant growth and
hospitals that outsource are seeing considerable cost savings while still
providing safe, quality patient care.
CHOOSING A REPROCESSOR
Some hospitals may choose to continue in-house reprocessing. However, those
that do must register with the FDA and follow premarket submission requirements
to show the efficacy and safety of each SUD it is reprocessing. The FDA is
taking steps to ensure that hospitals comply with the new guidance. In July
2002, the FDA issued a warning letter to a Tucson, Ariz. hospital for continuing
to reprocess SUDs without meeting the requirements.2
The decision to outsource reprocessing should involve stakeholders from all
areas of the hospital, including the operating room, infection control, risk
management and administration. Once the votes are in and the decision made, the
important question for hospital executives is: How do we maximize savings for
our hospital?
First, a hospital must perform due diligence in choosing a third-party
reprocessor. From the regulatory standpoint, reprocessors must comply with a
host of requirements, the most significant of which is the FDA's Quality System
Regulation (QSR) that controls all manufacturing processes, including cleaning,
disinfection, packaging, labeling, sterilization and distribution. QSR
requirements apply to both third-party reprocessors and device manufacturers.
Not all reprocessing companies are the same, however. Hospitals should look
for service and quality that go beyond FDA compliance. The Association for
Medical Device Reprocessors (AMDR), the trade group to which the three largest
reprocessing companies belong, recommends that hospitals ask a range of
questions before choosing a reprocessor. (See accompanying sidebar)
ROAD MAP TO SUCCESS
If a hospital is to maximize savings and reduce the amount of medical waste
destined for the landfill, it's important to have a plan in place for
implementing a reprocessing program. An implementation plan serves as a road map
to success and can help shorten the learning curve typically associated with the
launch of any new program.
Involvement of all key stakeholder groups is key to the program's success.
For that reason, the goals and benefits of reprocessing must be clearly
communicated to ensure that the program is embraced and supported at all levels
of the organization.
"If you don't have the key people and departments on board and ready to
begin, a program can falter and founder," said David Phillips, nurse
manager of surgical services at Horton Medical Center in New York.
"Reprocessing represents an opportunity for hospitals to see significant
cost savings. But you have to have hospital executives on board as well as
representatives from materials management, financial management, senior-level
management for managed care and department heads from areas where reprocessing
will take place."
Partnering with a third-party company to launch and maintain a reuse program
can benefit the hospital in the short term and in the long run. The company can
serve as a ready resource to help key hospital personnel anticipate challenges,
answer questions and fine-tune details. Company representatives should function
as liaisons in various areas, including device collection, in-service training
and utilization review to deliver maximum savings.
MEASURING SUCCESS
An effective implementation program guides an organization through the
planning, execution and management phases of a reprocessing program. Key steps
include creating a steering committee; developing policies and procedures,
setting up in-service training; and creating communications tools.
The plan should include steps for measuring the program's success. From
benchmarking and usage data, the reprocessor should be able to provide valuable
information about how well various hospital departments are complying with the
program. A facility also can use the information to determine its cost savings
and pinpoint areas where savings opportunities remain.
To be effective, the reprocessing steering committee should include senior
managers from operations, the operating room and infection control. In addition,
representatives from administration, central supply, the cath lab, the endoscopy
lab, materials management, nursing, the medical staff and risk management should
be included. A representative from the reprocessing company also should serve on
the committee. The panel's role is to guide the program, review and analyze
compliance, and identify areas for improvement. The chairperson should
understand the financial benefits and function as the "champion" of
the program within the organization.
PARTICIPATION IS CRITICAL
If a facility is to achieve maximum economic and environmental benefits from
reprocessing, participation across departments is critical. By providing clear
direction to department heads, the reuse committee can drive home the importance
of consistent collection of devices to be returned to the reprocessing company.
A reprocessing in-service and department orientation should be established
for each department, with specific staff training on proper collection of each
type of device to be reprocessed. In turn, staff must follow through by
consistently placing devices in collection containers. Selecting the appropriate
type and quantity of containers and locating them strategically and conveniently
throughout the facility will result in the highest collection rates.
In addition, the hospital should take steps to ensure reprocessed devices are
returned to inventory and chosen first off the shelves. One person - be it a
materials management inventory clerk or an operating room inventory clerk -
should be responsible for return and restocking of reprocessed devices. The
reprocessor should be able to supply reports to the hospital showing how
efficiently the facility is collecting and returning devices for reprocessing.
It is important to know what type of tracking information the reprocessing
company can provide. A reprocessor that has cleaned, tested and sterilized
millions of devices -- and tracked those devices by using unique identification
numbers -- can show the durability of the devices that a hospital is using. In
turn, that information may give a hospital insight on which manufacturers from
which to buy.
IMPORTANCE OF COMMUNICATION
Communicating the benefits of a reprocessing program helps to educate staff
and eliminate concerns based on perception rather than fact. At the program's
launch, the steering committee should meet with surgeons, department heads and
nurse managers to convey the goals and objectives of the program. The
organization's board of directors and medical staff should be notified by letter
or with a presentation.
The committee also should meet with the staff education and nursing
departments to determine the schedule and content of an in-service training
program. It's a good idea to prominently post notices about the reprocessing
program and display any other materials that promote the program and encourage
participation.
"Reprocessing is another avenue for a hospital to combat the financial
difficulties we're having with reimbursement, contracts and vendors,"
Phillips says. "If a hospital is going to reprocess successfully, it's
important to educate the staff on the systems being put into place."
An in-service program should be designed to familiarize department
supervisors and nurse managers with the program. They should have the
opportunity to ask questions and become comfortable with the practice of
reprocessing.
MONITOR AND REVIEW
The successful launch of an organization's medical device reprocessing
program is just the beginning. Once a program is underway, upper management and
the reuse committee must commit to evaluating participation and results. A
quarterly review of the program provides an opportunity to express concerns,
identify expectations and rate the performance of the facility and the
reprocessing company.
For optimum results from a reprocessing program, some key questions to ask
include:
- Is staff doing everything it can to ensure as many devices as possible are
collected?
- What economic savings have we realized so far, and what are our potential
savings?
- Is there potential further savings with regard to collection rates and
return to inventory?
- Are we communicating effectively through in-service education and other
tools?
Hospitals across the country are finding that reprocessing offers a
patient-safe, economic alternative with a proven safety record. Medical devices
represent one of the highest recurring expenses to hospitals after staffing.
Reusing, rather than disposing of, these expensive devices translates into cost
savings that can be reinvested in whatever providers may need to better serve
their patients, be it more nurses, new technology or other initiatives.
Deborah Haley is implementation and utilization manager at Vanguard
Medical Concepts, Inc., a national third-party reprocessing company based in
Lakeland, Fla. She has held numerous positions in perioperative nursing,
including staff educator and director.
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Ask The Right Questions
The members of the Association of Medical Device Reprocessors (AMDR)
work to ensure that their reprocessing practices meet all federal
regulatory requirements and, most importantly, are safe and effective. The
AMDR recognizes that significant differences exist among third-party
reprocessors, so to maximize the benefits of third-party reprocessing, it
encourages hospitals to ask the following questions before engaging the
services of a third-party reprocessor:
- Is the company registered with the FDA?
- Does the company comply with applicable Quality System Regulation
requirements?
- Will the company permit you to visit its plant and review its
quality manual?
- Is sterilization performed by a commissioned and certified
sterilization system, in accordance with ANSI/AAMI/ISO ST 11135 ST
1994?
- Is the sterilization cycle re-qualified annually?
- Are biological indicators used to monitor routine sterilization?
- Are the sterilization systems routinely calibrated?
- Is the residual sterilant level routinely tested?
- Does the company have reprocessing procedures tailored to the
specific types of medical devices you wish to have reprocessed and has
the company validated these procedures?
- Is the product functionality routinely tested?
- Does the company track the number of uses per device?
- Does the company comply with medical device reporting requirements?
- Does the company have adequate liability insurance coverage?
Source: AMDR |
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