MRI
of 69-year old male with low back pain, reveals an increase in disc
height and a decrease in size of disc herniation after treatment with
the DRX9000™
It
is estimated that Americans spend at least $50 Billion each year on low
back pain and it is the second most common neurological ailment in the
United States.¹
With these staggering numbers, the DRX9000 True Non-surgical Spinal Decompression SystemTM was
developed to provide an effective non-surgical treatment
alternative for chronic low back pain patients. Furthermore,
recent studies have demonstrated the DRX9000's ability
to potentially decrease analgesic use for chronic low
back pain patients.
A newly published case report in Volume 2
Issue 1 of the European Musculoskeletal Review, demonstrates positive
results utilizing the DRX9000 True Non-surgical Spinal Decompression
System. The report titled, "Managament of Low-Back Pain with a
Non-surgical Decompression System (DRX9000) - Case Report" displayed
the pre- and post-treatment MRI findings of a 69-year old male with low
back pain.
Prior to the DRX9000 treatment, the patient
described experiencing low back pain radiating in both legs. When asked
to describe his pain intensity on a scale of 0-10, the patient rated
his pain intensity at 10. After completion of 22 treatments, over a
seven-week period, the patient reported a pain intensity level of 1.
What's
more fascinating is the fact that four months after the initial visit,
a follow up MRI revealed decreased herniation size and increased disc
height at multiple lumbar levels.
The authors conclude the case
report by stating, "This case report further builds on previous
findings that have demonstrated improvements in disc morphology after
treatment with the DRX9000."
To view a copy of this case report, please click here. ¹ National Institute of Neurological Disorders and Stroke, National Institutes of Health, "Low Back Pain Fact Sheet," July 2003.
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From our ears, to your practice
While
we strive to provide all of our clients with the finest customer
service possible, we do receive ongoing feedback on how we may
continue to improve our products and services. In doing so, many of our
physicians have commented on how they strive to improve customer
service in their own practice. As a result, we thought we would
share some of those ideas with all of you.
Has
there ever been a time where you have spoken to a patient and
never heard back from them again? Does it make you wonder if it was
something you said or didn't say? Or was it a staff member that may
have forgotten to greet the patient as they walked in?
The
following are tips given to us by your colleagues, on how to find out
if you're meeting your patients expectations of customer service:
Tip
#1: Create a 5 question Survey for your patients to fill out after
their consultation or treatment. Give them a free promotional gift for
participating, such as a pen or a stress ball with your clinics contact
information (this exercise has two purposes; it allows you to receive
feedback from your patients, and it gives you free advertising)
Tip
#2: Add a comments/suggestions box at the front desk where your
patients can anonymously provide feedback on their experiences in your
practice.
Tip
#3: At one of your staff meetings, have your employees give suggestions
on how to improve your overall quality of service. Offer an incentive
to the employee that offers the most productive ideas.
These
tips can help your practice improve the quality of service demanded by
patients, and in return help draw new patient referrals.
If you would like additional information or tips please contact the Customer Care Center at customer@axiomworldwide.com. We look forward to hearing from you.
Are you looking for an alternative pain relief product?
Learn more about Essential Oxygen Oil™ intended for temporary relief of minor aches and pains!
Essential Oxygen OilTM
helps reduce pains and aches associated with arthritis, simple
backache, strains, bruises, sprains and leg cramps. Without sufficient
oxygen, your muscles will reduce glucose into lactate and release
hydrogen ions into the muscles that cause lactic acid build up, leading
to pain, cramps and muscle fatigue. Applying the Essential Oxygen Oil
to these areas will transport oxygen where it is deficient to restore
oxygen supply and reduce inflammation in cells. Improved oxygen supply
can assist physically stressed areas of the body in natural healing.
To
apply, you simply massage the affected areas generously 2 to 3 times a
day. The Essential Oxygen Oil is so well absorbed you are not left with
the greasy feel that some other over the counter products can leave you
with. The oil is all-natural and contains no steroids. The
natural herb it contains is in the family of groundnuts, similar to
peanuts.
Many
prescription pain relief products have negative side effects such as
(but not limited to): increase in heart attack or stroke, ulcers and
bleeding, and other cardiovascular and gastrointestinal damage. With
the Essential Oxygen Oil, you obtain relief without those potentially
fatal side effects and you can use the product long term.
Essential Oxygen Oil is recommended for use before and after
physical exercise or any activity that puts strain on muscles, joints
and tendons. It is also great to use in conjunction with massage
therapy and patients being treated with the DRX9000 True Non-Surgical
Spinal Decompression Therapy.
The
makers of Essential Oxygen Oil, CreoMed, Inc, are dedicated to
providing their clients with the highest quality products that are
created from a sound scientific foundation, the science behind nature.
They recognize and join today's consumer in the quest for natural
health remedies and offer an innovative family of products that are
proven and clinically tested. To learn more about Essential Oxygen Oil
and CreoMed, Inc, please visit www.creomed.com or call 866-750-CREO.
Medical Disclaimer
All
information on this newsletter is intended for your general knowledge
only and is not a substitute for medical advice or treatment for
specific medical conditions. We can not and do not give you medical
advice. We do not recommend the self-management of health problems.
Information obtained by using our products or services is not
exhaustive and does not cover all diseases, ailments, physical
conditions or their treatment. Should you have any healthcare related
questions, please call or see your physician or other health care
provider promptly. You should never disregard medical advice or delay
in seeking it because of something you have read here.
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Axiom Worldwide's Marketing Authorization Holder (MAH) Receives Marketing License for the DRX9000™
Japan's
Pharmaceutical Affairs Law (PAL) harmonizes the requirements of various
international regulatory requirements and reduces the conflicting
demands of these various regulations by incorporating the guidance
documents of the Global Harmonization Task Force (GHTF). To sell
medical devices in Japan, the PAL requires that two licenses be
obtained. The device manufacturer must first obtain manufacturing
accreditation for their manufacturing facilities. Second, a marketing
authorization holder (MAH) must be assigned the responsibility for
safety and effectiveness of the medical device in Japan.
Axiom
Worldwide's foreign manufacturing accreditation certification was
received on October 31, 2007. This includes quality management systems
(QMS) requirements based on ISO 13485:2003 with additional requirements
stipulated from the Japanese Ministry of Health, Labor and Welfare
(MHLW) from Ministerial Ordinance 169. Axiom's foreign manufacturing accreditation covers the manufacturing of products for the Japanese market.
Axiom
Worldwide's Marketing Authorization Holder (MAH) received the Marketing
License for the DRX9000™ on May 8, 2008. Obtaining a device license
involves an evaluation of technical documentation for the designated
medical device. This is similar to the requirements outlined in the
Global Harmonization Task Force's Summary Technical Documentation for
Demonstrating Conformity to the Essential Principles of Safety and
Performance of Medical Devices. The MAH
must also demonstrate an effective quality management system in Japan,
separate of the manufacturer, and be assessed for conformance to
Facilities requirements (MHLW Ordinance #2) and GMP Requirements (MHLW
Ordinance #169).
Japan
has very specific policies and stringent processes in place to make
sure that medical devices sold in Japan are safe and effective. Axiom
Worldwide has met one of the most demanding quality standards in the
world. Having met the regulatory requirements in Japan is a testament
to the company's worldwide commitment to manufacture quality
non-surgical products that are safe and effective in treating patients
suffering with chronic back pain.
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Kay Ball, RN, MSA, CNOR, FAAN
My
back problems began in 1989 when our van smashed into the side of a
flatbed truck. While the seatbelt I was wearing saved my life, the
impact left me with some major injuries.
The first part of my
small colon ruptured leading to peritonitis and pancreatitis. The force
of the collision broke a spinous process on my back and realigned my
vertebrae in the lower spinal area. In 2004 (15 years after my
accident), I was diagnosed with advanced degenerative disc disease from
L2 through S-1.
As the pain progressed, my spinal orthopedic
surgeon recommended a series of treatments to avoid surgery. I had
weeks of physical therapy, took large amounts of prescription pain
killers, had two spinal injections, and acupuncture all in the span of
a year.
The pain only became worse.
As a
surgical nurse, I'm constantly on my feet. I also travel
extensively throughout the world lecturing on laser technology and
endoscopy. My back problems were not willing to comply with my
busy schedule, and I wasn't about to give up.
As my quality of
life continued to decline, I reluctantly decided that surgery was my
only option. The spinal fusion was scheduled.
I e-mailed a
friend about my upcoming surgery. She immediately protested and
told me to search DRX9000™ online to find out more about it. Knowing I
had nothing to lose, I did as instructed. I was pleasantly
surprised to learn about this amazing state-of-the-art technology.
Within minutes of emailing Axiom for more information, I got an email
reply with a doctor that was about 7 miles from my home. I was seen the
next day. What service!
From the moment I walked through the
door, my needs, questions, and concerns were addressed. After having
more x-rays to determine if I was an appropriate candidate for
treatment, my doctor commented that my back would be a challenge but he
thought I would benefit from the treatments. I started the next
week. After only one week, I began to notice a decrease in pain.
Over the next couple weeks, the pain became a discomfort, and now it's
only an annoyance. I continue to be treated and continue to be
astounded at the success of the DRX9000™ treatment program.
I
strongly recommend this technology for anyone who is experiencing back
pain or contemplating surgery. As a surgical nurse, I know the
consequences of spinal procedures and have seen the successes and
failures of surgical intervention. I know the recovery time
involved. Being able to avoid spinal fusion was critical for me and the
DRX9000™ made that option possible. Thank you for developing and
promoting this technology.
What a gift for better clinical outcomes and less invasive patient care!
To find a DRX9000™ physician near you, please click here.
MKT0230 REVA
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DRX9000™ Patient Success Stories
Watch and listen to real life patients discuss their personal experiences with the DRX9000™
UPDATE - Which Electrical Stimulation Device Is Right For Your Patients?
We would like to announce that since this article ,
published in Issue 2 - Winter 2007 of Axiom's Better Health
newsletter, the format of the EPS8000 & NVP8500 has changed.
The EPS8000 & NVP8500 are now available without the accessory cart,
as shown below.
Electrical
stimulation via either the EPS8000 or NVP8500, and venturi electrode
application via the NVP8500, remains unchanged. The new form
factor satisfies customer requests for smaller units that can utilize
existing space in clinics. A venturi electrode tray adapter (not
shown) comes standard with the units. A simple accessory cart
which accommodates the dimensions of the EPS and NVP units is available
as an option.
Axiom
continues to update its product line based on your feedback.
Axiom's customer base indicated they did not require a complex, larger
cart with accessory shelving. The new footprint for the
EPS8000 & NVP8500 addresses this request, and still
carries all of the regulatory and quality certifications Axiom
customers have come to expect.
Contact Axiom Worldwide at 877-438-0663 or visit us at www.AxiomWorldwide.com to find out more about the latest sales and pricing on these devices.
At Brican, we take a "Wellness" or "Lifetime Care" approach to Patient Education
Transform
how you market your Chiropractic care and products at your office and
in your community. Through our very affordable program it is our goal
and purpose to help you develop and maintain a new enthusiasm for
Chiropractic among all those who seek your care.
Mediadoc™
brings patient education and excitement in the office, capitalizing on
every minute spent by the patients before and after their
adjustment. Mediadoc™ will
give your patients a greater understanding of what you do, so that they
can more fully appreciate the real value of the adjustment improving
patient retention and generating new referral business.
Mediadoc™ a
top of the line patient education system with over 13,000 captivating
visual messages, 3000 backgrounds, powerful testimonials and product
marketing features which is a modular system adaptable to any room
configuration and starts to work for you immediately upon installation.
Some of its exclusive features are ability to program several
shows at the same time and send different program selections to run in
separate rooms, calendar advance programming feature, built-in create a
slide and digital camera feature.
For more information call 1-800-644-1055 ext. 28 or visit us at www.bricancorp.com
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General DRX9000™ Lumbar Applications Guidelines
The
generalized guidelines below are to be used solely for the
informational purposes of the healthcare provider and this information
should NOT be relied on by non-professionals to make medical decisions.
All decisions regarding diagnosis, treatment, management, and
rehabilitation are the ultimate responsibility of the licensed
healthcare provider.
(DRX9000™ SYSTEM)
INITIAL LOADING SUGGESTIONS
DAY-1: One half total body weight minus ten to twenty pounds. DAY-2: One half total body weight. DAY-3: One half total body weight plus ten pounds.
SUBSEQUENT TREATMENTS: One half total body weight plus ten pounds.
Loading
guidelines may not be appropriate for all patients. Determination of
all treatment parameters are at the discretion of the licensed
physician. Not all patients with back pain are candidates for treatment
with the DRX9000.
The
above loading suggestions are general guidelines only. All treatment
parameters must be determined in accordance with patient comfort and
tolerance. DO NOT be afraid to use lower distractive loads if the
patients condition warrants. The treatment objective is to reach the
therapeutic load of one half total body weight plus ten pounds, however
some patients may not achieve this goal. It is common for the
progression toward a therapeutic load to require more than three days.
Also, favorable outcomes may still occur if the patient is able to
achieve a therapeutic response although unable to reach one half total
body weight plus ten pounds.
All
medical treatments and procedures have potential side effects.
Treatment should be suspended for any patient exhibiting signs or
symptoms of side effects and/or adverse reactions pending physician
re-evaluation and the determination that continued treatment is
appropriate. Under certain conditions patients treated on the DRX9000
may experience minor side effects consisting of transient discomfort or
soreness.
CAUTION: Safety
necessitates a thorough understanding of the patients clinical
presentation and physical characteristics. All patients undergoing
non-surgical spinal decompression must have a thorough workup which
includes a comprehensive history, complete review of systems,
comprehensive physical examination, review of previous medical records,
regional x-rays and stability studies, MRI imaging and other pertinent
testing to rule out any red flag issues, quantify yellow flag issues
and exclude known contraindications prior to treatment. It is the
responsibility of the physician to determine the probability of a
successful treatment outcome for each patient. Tissue characteristics
such as disc viability or nerve viability as well as other pertinent
health factors should be taken into consideration. Clinical decisions
based on an individuals weight must be tempered by the patients ability
to tolerate the prescribed treatment and weighed against the risk of
possible injury. Exercise further caution when considering initial
distractive loads greater than 100 pounds. Always weigh the potential
benefits against potential risks.
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Are you receiving consistent MD patient referrals?
As
we continue to grow as an organization and provide valuable research on
the efficacy of the DRX9000™ you will find that the number of medical
doctors recommending this form of treatment will increase.
Until
then it is up to those who offer the DRX9000 treatment to
educate the primary care physicians, pain management physicians
and other physicians about the DRX9000 therapy. In doing so, you
will find that many MD's will begin referring his or her
chronic low back pain patients to your practice.
One of the most
important things to remember when it comes to medical doctors is that
they only want to see peer-reviewed papers, abstracts and
articles. They are not interested in listening to theories
or personal belief, but simply wish to review the scientific
data.
In order to facilitate the process of gaining
recognition from medical doctors in your community and educating
them on the DRX9000™ treatment, we have developed a 5 Step MD
Referral Program for you to utilize.
You can implement our 5 Step Referral Program immediately, with the cooperation of your next DRX9000™ patient.
To view a basic outline of our 5 Step MD Referral Program, please click here.
If
you're a DRX9000™ physician and would like to receive a copy of the
entire 5 Step MD Referral Program, please contact Amber Pacetti at apacetti@axiomworldwide.com
Our
marketing department will begin featuring a new marketing
program on each of our Better Health e-newsletters. Please submit any
of your requests or suggestions to marketing@axiomworldwide.com
Recent Press Releases
Axiom Worldwide CEO Featured In The 24th Edition Of Zillion Business Review!
The benefits of Axiom Worldwide's DRX9000™ Non-Surgical Spinal Decompression System exhibited at the 24th National Space Symposium.
Recent DRX9000 Published Articles
Axiom Case Study Yields Favorable Findings With Back Pain Device FDA news - Falls Church,VA,USA
It's a stretch: Back-pain sufferers seek relief in therapy under dispute CommercialAppeal.com - Memphis, TN
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