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PROGRESSIVE MEDICAL
Contact: Melanie P. Arledge
760-448-4448
www.progressivemed.org
Progressive Medical
Using Technology to Boost Crucial Compliance Rate
The criteria and guidelines in the treatment
of Sleep Disordered Breathing (SDB) have finally been dragged into
the 22nd Century, albeit kicking and screaming. What does this mean
to the companies who don't have a solid compliance program in place?
Increased cost, decreased revenue!
In yester-year Home Medical Equipment Companies
(HME's) relied upon the patient's word as to how they felt and how
many hours a night they used therapy. Hour meters were the next
best thing in the progression, however, this advancement wasn't
full proof either, patient's realized they could just run the motor
without utilizing the therapy, just give the reading to the HME
of hours used. Therefore left untreated, the patient's disease process
continued in a downward spiral but the HME's were reimbursed by
the Carriers. HME's cost were minimal; the PAP's were simple blowers,
the overhead to the company was low do to the fact they could staff
unskilled employees. Compliance rates were also low; approximately
30-40% of patients actually utilized therapy.
Only within the last 7 years have companies
had the luxury of utilizing smarter PAP devices that are downloadable.
Of course these devices were more expensive leaving the HME's to
absorb the cost while at the same time reimbursement from the Carriers
decreased. Along with the improvement of technology came the need
for skilled employees to decipher the information. Did compliance
improve with these advancements? Not necessarily. Sure we had the
ability to extract the data whether it was the "law of averages"
or "real-time", the information was forwarded to the carriers to
prove compliance for reimbursement but efficacy was lacking. With
the advancement in technology and the increased cost of skilled
employees, Compliance rates only increased slightly; 40-45%.
Progressive Medical's compliance rate is one
of the highest in the industry; 90% and higher. How do we achieve
this? Through education and efficacy of therapy. It isn't enough
to absorb the cost of more expensive PAP devices and skilled employees,
the patient must be educated on their disorder and the physiological
ramifications of untreated Sleep Disordered Breathing (SDB). We
have an extremely tight program starting with the initial order
and intake. There is no need to worry about compliance, it is a
given, when we empower the patient with knowledge! Not only are
our employees skilled and registered in their field, they are investigators
who are trained to discover what isn't readily addressed through
little to no pertinent medical history. No stone is left unturned,
we insist on significant others being present at the initial appointment
to gather information that the patient is usually unaware of. If
the Sleep Study was performed by an outside entity, the pressures
are verified through the current technology of "real time" downloads.
If the pressure isn't effective, Progressive Medical requests the
ability to re-titrate the patient to find the appropriate pressure
and device needed from the referring physician. Post discovery the
physician is notified of the findings, the patient is set on effective
therapy and our tight follow up program is implemented.
The new AASM recommendations commencing July
1, 2009, state patient compliance must be proven quarterly in the
first year and then annually. This has not been an Industry Standard
and many HME's and Sleep Labs are going to be left holding the bag
of denied claims. The answer to the HME's who want to succeed with
the new stringent guidelines need to follow suit. While this might
seem to be a hardship to companies not set up to handle the new
criteria, it is a tremendous benefit to the patient and further
down the line, the HME. Having knowledgeable staff trained to meet
the individual needs of a patient and empower them to make a positive
impact in their own lives by taking ownership through education
and effective treatment, compliance isn't an issue. Healthy living
becomes the patient's lifestyle and compliance is a given. Therefore
the improvement in technology utilized to prove compliance is worth
its weight in gold to the HME. The new AASM recommendation opens
the door wider for Savvy HMEs to become in-valuable to their local
Sleep Labs by assisting the Lab with an effective follow-up program.
It is essential for the Accredited Sleep Lab to meet the following
criteria; patients initiated on PAP therapy must have objective
data from the device in an effort to trend patterns and remediate
problems. Again at the 12th week of use and quarterly thereafter
for the first year.
Melanie P. Arledge, Progressive Medical
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