Monofiliments Not an Accurate Test of Neuropathy (Lee Rogers, DPM)
10/22/2008 Peter J. Bregman, DPM, James J DiResta, DPM,MPH
RE: Monofiliments Not an Accurate Test of
Neuropathy (Lee Rogers, DPM)
From: Peter J. Bregman, DPM, James J DiResta,
DPM,MPH
With all due respect to my colleagues, I am not
promoting the PSSD machine and while I do
perform nerve decompressions for people with
painful neuropathy both diabetic and non-
diabetic I am not advocating the machine for
anyone. Dr. Rogers is correct regarding LOPS and
seems to be looking to be argumentative towards
me regarding the mono-filaments. I assumed that
all reading my post would understand that I was
referring to loss of protective sensation
(neuropathy ) rather than neuropathy itself. If
I did not make it clear then it is now.
The studies he referenced are, in my mind, not
based on my experience and are presented by
people who choose not to believe the 8 or so
published articles on nerve decompression
surgery that have been published and are
consistent. They are not the double-blind
randomized prospective studies that people are
looking for but they are good enough for me and
I have stacks of letters from patients and
please even view my website for video
testimonials from my patients who have had the
surgery.
Dr. Rogers chose to attack the surgery with the
usual rhetoric of the “non-believers”. In my
experience the non-believers are not surgeons,
so their toolbox is limited. They also have a
lot of money to lose if patients can be treated
with surgery and do not need expensive emg/ncv
testing and can get off the neuropathy
medications. I cannot tell you how many times I
have had a “Negative EMG” and performed
decompression surgery despite this so called
negative test and the patients do well 85-90% of
the time.
The PSSD machine is sensitive and an early
detector of neuropathy. Yes, it is expensive I
cannot argue with that. As for the learning
curve to be able to use it properly I guess you
just have to accept the training that comes with
it for which you get certified to do. Dr.
Dellon by the way has recently responded to
recent position statements by the Neurologists
and the ADA. I am attaching two articles written
by Dr. Dellon which elucidate in a clear manner
the arguments here. Also, it should be know
that as we (Association of Extremity Surgeons)
are preparing to do the prospective randomized
study on the decompression surgeries. I have
little doubt it will end the debate over this
unless you just want to deny the results no
matter what they say.
I would ask Dr. DiResta not to infer that I
think the PSSD is the Gold Standard for
Neuropathy detection. I simply said and quite
clearly that Monofilaments are not. I would like
to know how it finds false positives if done
properly? I do not appreciate the clear
inference that I or one of my colleagues would
perform surgery on someone who was not a
candidate for the surgery just because they had
a positive PSSD test. They need to have the
physical compression of the nerves to benefit.
Please refer to the attached papers from Dr.
Dellon. As for the cost of the PSSD to the
health care system Dr. DiResta you don’t see the
big picture.
First of all, it is significantly cheaper than
EMG/NCV studies which are not accurate for lower
extremity testing for tarsal tunnel and
compression neuropathies. Also, if you can put
away your biased opinion on the PSSD machine
which is FDA-approved and covered by Medicare in
most states you might understand the bigger
picture. Billions of dollars are spent on
treating ulcers and the resultant amputations
etc. If we can stop ulcers from occurring in
the first place then we save the system Billions
of dollars and give patients a better quality of
life. See the Neuropathy Registry on
www.Dellon.com and you will see that patients
whom underwent decompression do not get ulcers
just a very small percentage. This is fact.
In closing, I did not want to get into this
discussion but I felt compelled to respond. I
can say that I have used the PSSD machine and
Monofilaments and treated patients with
Neurontin and other modalities and performed
surgical decompressions done the Dellon way.
Have you also had this experience? I feel like I
can speak about both with equal experience.
Please show me all of the studies on how aspirin
works on curing headaches? We know it works but
there are no double blind randomized studies on
this so should we not take aspirin for
headaches?
As far as the surgery being in dispute this is
only by people who don’t do it. Please let
anyone who was trained by Dr. Dellon who had
performed more that 20 of these procedures come
forward and tell us how it does not work. How
many people are still using Anodyne treatment
despite the articles showing it does not work? I
will continue to use my experience in practice
and continue to perform these surgeries on the
appropriate candidates and make a difference in
their lives as evidenced by the fact that they
have said on camera they are better. I have
received numerous letters from them thanking me
for changing their lives and they come back to
have the other side done. If these procedures
did not work why would this be? How many of you
inject “neuromas” with absolute alcohol
injections? Show me the double-blind studies on
that? I am sure I will get even more responses
now and I think I shall wait until our study is
finished before continuing this debate.
Peter Bregman, DPM, Tewksbury , MA,
footguru@comcast.net