Meeting Medicare Quality Standards
By Daniel Gurley, AOPA Government Affairs Department
Daniel Gurley is manager of
regulatory affairs in AOPA’s Government Affairs department.
Questions? Contact him at (571) 431-0812 or dgurley@AOPAnet.org.
Do you have questions about the new Medicare Quality Standards? These
standards were introduced in conjunction with the durable medical
equipment, prosthetics, orthotics and supplies (DMEPOS) competitive
bidding program that was first mandated by the Medicare Modernization
Act of 2003.
CMS has stated that the quality standards and accreditation
requirements must be met by all O&P providers sometime in the near
future, though no specific deadline has been given and O&P is not
included in the current round of competitive bidding. We know
you’re concerned about how these standards will
affect your practice, and what you can do to prepare.
Here are some answers to common questions AOPA receives about the quality standards:
Q: Why does Medicare want to implement quality standards? How are they going to help patients and providers?
A: CMS believes that implementing quality standards will:
Q: Don’t I only have to implement the quality standards if my facility participates in competitive bidding?
A: Currently, only participants
in competitive bidding must meet Medicare Quality Standards and be
accredited. However, at some point in the near future all DMEPOS
suppliers must meet the standards, even if they don’t participate
in competitive bidding.
At press time, CMS had not yet developed a timeline for DMEPOS
suppliers not participating in competitive bidding to implement the
quality standards. However, no one is sure of the amount of lead time
that CMS will provide before implementation. The best thing to do is to
get an early start on reviewing and implementing the Quality Standards.
| For More Information |
| Still have questions? Copies of the Quality Standards are available on the CMS Web site at www.cms.hhs.gov/CompetitiveAcqforDMEPOS/downloads/CMS_DMEPOS_Quality_Standards_081406.pdf. |
Q: How do the new Quality Standards affect my facility?
A: Most facilities will find
that, if they are currently meeting accreditation and Medicare supplier
standards, they are also meeting the majority of the Quality Standards.
AOPA is working on “crosswalking” the Medicare Quality
Standards to both the Medicare supplier and accreditation standards,
combining and comparing the requirements from each souce. AOPA will
publish this information in an upcoming guide.
Q: The new quality standards
state that facilities and companies should have one or more persons in
place to perform leadership functions and direct the organization and
its key activities and operations. Will this standard change the
existing leadership structure of my company/facility?
A: In the standard, CMS
defines what it considers “leadership.” For example, the
leadership structure can be a single owner/employee or a management
team reporting to a corporate headquarters. The standard just ensures
that one person, or a group of people, are responsible for basic
company function and control, so even small providers may not need to
change their current structure.
Q: The standards keep referring to delivery and setup requirements. These are not applicable
to my facility. What should I do?
A: The Medicare Quality
Standards are written in several parts: “Business
Services,” “General Product-Specific Service
Standards” and three appendices, of which “Appendix C:
Custom-Fabricated, Custom-Fitted, Custom-Made Orthotics, Prosthetic
Devices, Somatic, Ocular and Facial Prosthetics, and Therapeutic Shoes
and Inserts” is relevant to AOPA members.
The first two sections are meant to be general and address all types of
DMEPOS suppliers. This is the reason that several requirements do not
seem to fit O&P suppliers. CMS is aware that not all suppliers will
be able to meet requirements that are not related to their services.
