Surgery Sometimes, Bracing
Often, Caution Always
Caring for the CMT-Affected Foot
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Orthopedic surgeon Robert Meehan examines the foot of a man with CMT. |
by Margaret Wahl
Diane Lareau, 35, of Linwood, Mass., always
knew there was something wrong, but her mother kept telling her she
was just pigeon-toed and that putting her shoes on the wrong feet would
fix the problem.
It didn’t, and by her late teens, she remembers, her
toes were “all bent and just a mess. It looked like a bird’s claw on
both feet. I was actually almost walking on the outsides of my ankles.”
She also had extremely high arches, so that her feet looked like humps.
Lareau finally saw a specialist in her senior year of high school, with
urging from the school nurse, and the problem acquired a name: Charcot-Marie-Tooth
disease, or CMT (see “Faulty Wiring").
“They gave me these hard plastic insoles to put inside
your shoes for support for the arches, supposedly to help you walk.
Those didn’t work so great.”
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The
typical CMT-affected foot has a high arch
and “hammer” toes. |
Later, in her late 20s and pregnant, Lareau fell from her front
porch and wound up in the emergency room. The only good thing about
the experience was that a doctor there referred her to an orthopedic
surgeon who understood the problems of the CMT-affected foot: weakness,
some loss of sensation, and progressive changes in shape caused by the
action of muscles that aren’t receiving the right nerve signals.
Keeping It Simple
In CMT, “the typical problems with feet are the shape
of the arches and the difficulties with the joints that walking with
abnor-mally shaped feet causes,” says neurologist Michael Shy, an MDA
research grantee at Wayne State University in Detroit, where he also
co-directs the adult MDA clinic and directs a special CMT clinic. “Not
every single person who has CMT has high arches. Some people have flat
feet. But many patients have abnormal feet.”
Another common problem is hammer toes, so named because
the toes are curved into a shape resembling the hammers that piano keys
activate.
Patients’ needs vary, Shy says. Some can get by with
simple inserts in their shoes, while others need ankle-foot orthoses
(AFOs), which are lightweight (usually plastic) braces that stabilize
the lower leg and foot.
Only a minority of people with CMT-related foot deformities
need surgery, Shy says.
“In my opinion, when foot deformity is so severe that
patients walk on the sides of their feet or when [a high arch] is ex-treme,
it’s worth considering surgery,” Shy says. “Also, when hammer toes are
so severe that patients are developing calluses or blisters on the tops
of their toes, many would consider surgery to straighten the toes.”
The Wayne State clinics provide what Shy describes as
“a little bit of a unique resource.” Treating patients from 37 states
and some 15 countries, the specialists in every aspect of CMT start
with a conservative approach before venturing into surgical territory
to treat CMT.
“Generally, we start with shoe inserts and AFOs” to
align the foot, Shy says.
Shoe Inserts
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Foot orthotics can often realign the pronated or supinated foot, reducing stress on weight-bearing joints. |
“It’s extremely uncommon that somebody doesn’t need some sort
of orthotic,” says Steven Hinderer, a physician specializing in physical
medicine and rehabilitation at Wayne State. (An orthotic, or orthosis, is any supportive device, although the first term
is more often used to mean a shoe insert and the second to mean other
kinds of appliances.)
People with CMT also need a good walking or athletic
shoe with a removable insole to make room for the orthotic, Hinderer
says. He likes New Balance and Brooks shoes.
“We recommend that people take hold of the shoe and
try to twist the forefoot on it. If it’s flexible, it’s not going to
give you the support you need. You want one that’s fairly rigid.”
The key to foot orthotics, he says, is “to get the ankle
and hindfoot in as close to neutral, or normal, alignment as we possibly
can.”
If the patient is walking on the outsides of the feet
— supination — or the insides — pronation — Hinderer
generally puts a small pad on the bottom of the foot orthosis. “We’re
holding the whole foot in good alignment. The advantage is that it puts
the weight-bearing joints [where bones meet] into their normal position
so they’re not being given extra stress.”
If there’s any flexibility left in the foot, Hinderer
says, there’s usually a way to hold it in better alignment. “Orthotists
[brace makers] are pretty creative folks.”
Ankle-Foot Orthoses
But misshapen feet and weak ankles aren’t the only problem
in CMT.
Another common factor in the disease is a weakening
of the muscles in the front part of the lower leg, those that pull the
front of the foot back and off the ground during walking. When those
muscles are weak, the foot tends to flop down as the person walks, so
that he trips over his own feet.
When foot drop is the first problem in CMT, Hinderer
says, an off-the shelf type of AFO, made of strong, light carbon fiber,
works well.
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Diane Hardin, 57, holds one of her plastic, open-backed AFOs, which she says give her more flexibility than orthoses that run up the back of the leg. |
“They’re not a custom fit, but they’re very thin, very
lightweight, and from that standpoint very nice,” Hinderer says. “But
more often than not, we see folks who have had foot changes already,
and that off-the-shelf type of device doesn’t accommodate the foot changes
at all.”
A custom-fitted, plastic AFO with a hinge at the ankle
joint — for uneven ground, stairs and driving — is probably the most
commonly prescribed device.
As for vertical support, Hinderer likes AFOs that go
up the back of the leg, although, with a carbon fiber AFO, he says,
you can make some that go up the sides and come around to the front.
“We like a symmetric arrangement, either up the back or up both sides.”
Carbon fiber AFOs are stronger and more expensive than
plastic but provide more options. “You can do more at the ankle with
how you adjust and position,” Hinderer says. “And in terms of design,
it’s more open. It’s cosmetically perhaps a little better.”
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In
the triple arthrodesis procedure, three joints
(A, B and C) are fused and immobilized, holding
the foot in a corrected position. The operation
is performed less often now than in the past,
because it interferes with the foot’s
ability to act as a shock absorber. |
A single standard plastic AFO, Hinderer says, goes for about
$500. Carbon fiber AFOS are about double that. Insurers usually pay
for AFOs, but not for shoe inserts.
“The biggest thing is that orthotics must fit extremely
well to be effective,” Hinderer says. “People will tolerate orthotics
that don’t fit well and keep trying to wear them. They’ll say, ‘I wear
them three hours and they’re killing me.’ It shouldn’t be that way.
If it’s fitting really well, the way it should, you should forget it’s
on.”
Michael Shy cautions his patients to beware of “miracle”
braces. “None of these work for all people,” he says. “Advertising for
special braces should be viewed with caution.”
When Diane Lareau read about carbon fiber AFOs on the
Internet, she decided to have some made for her, at a cost of $1,200
each. Fortunately, her insurance company paid for them.
“I was excited because they’re supposed to be so strong,
but what they don’t tell you is there’s no support for your heel. They’re
just a flat base.”
For the new AFOs to work for her, Lareau found out she’d
need to wear them with shoe inserts, which cost at least $150 each and
which her insurance won’t pay for. “So, unfortunately,” she says, “these
babies are hanging in my closet until I can get the money to get them.”
She’s staying with her old AFOs for now.
Surgery
Steven Hinderer says foot surgery is “something people
should hold off on, in my opinion, until they’ve really pursued good
orthotic fitting, and, if need be, physical or occupational therapy
to supplement that.
“If they’re not getting the results they want, then
perhaps surgery is a consideration. But most often we’ve been able to
accomplish a great deal with noninvasive methods.”
When Hinderer or any other member of the Wayne State
team wants to get an opinion about surgery, he’s likely to call Robert
Meehan, an assistant professor in the Orthopaedic Surgery Department
at WSU, and a specialist in repairing feet and ankles.
Meehan doesn’t rush into surgery either.
“Typically you start off with conservative measures
first,” he says. He recommends a trial of changing shoes and bracing.
If those don’t work, “then you talk surgical options, typically,” he
says.
“If a patient comes to me with the fact that they’ve
broken maybe two or three braces during the course of a year, and [the
braces] aren’t holding the deformity, that’s a case where you’d start
thinking about surgical options.”
In general, Meehan advises people to postpone surgery
until they’re in their 20s or 30s, because muscle imbalances in CMT
are still evolving over time. “If they feel the deformity is progressing
and it’s unbraceable, then we recommend it,” he says. “But we don’t
recommend it as a preventive measure.”
Phasing Out Fusions
“Foot surgery is common in CMT, but the types of foot
surgery performed are changing,” Michael Shy says.
“One or two generations ago, many of the procedures
were a triple arthrodesis, which involves bone fusions to stabilize
ankles. These are done less frequently now. There’s a concern that any
surgery involving bone fused to bone will cause signifi-cant arthritic
problems, including pain, after a number of years.” (Arthritis is any
inflammation of the joints.)
Instead, current surgical approaches more typically
involve tendon transfers [moving tendons] and procedures to correct
the angle at which the foot strikes the ground, Shy says, in an attempt
to prevent future arthritic complications. (See “Moving
Tendons.”)
“When children had triple arthrodeses in the past, it
was a horrible thing, because it knocked out their growth plates and
left them with a short, stubby foot,” Meehan says. That kind of procedure
can lead to arthritis by early adulthood, he says.
Another woman with CMT, Diane Hardin, now 57 and living
in Madison Heights, Mich., remembers having triple arthrodeses on both
feet back in 1961 in Ohio, when she was 12 years old.
“I was so pigeon-toed that I tripped over my own feet.
I would step on each foot as I walked. It was just called birth defects
at that time.” Her doctor, wisely, told the family to wait until she
was fully grown before attempting to fix the problem. “I wasn’t diagnosed
[with CMT] until after the birth of my second child.
“Basically, my feet are completely fused except for
the ankle and one joint in the center,” she says, “so I don’t have a
lot of flexibility. I walk very flat-footed because of it.”
Until she was well into adulthood, it didn’t seem to
cause many problems. “I honestly would not have been walking all those
years at all if it was not for the surgery,” she says. But as she got
older, things began to bother her, particularly her left hip and her
back.
Her left leg, it was found, is about half an inch longer
than her right, something that occurs in the general population fairly
often. But that small problem plus the fusion of her feet bones may
have been an unfortunate combination.
The joints of the back of the foot, Meehan says, “control
a lot of your side-to-side motion, and they’re a big part of shock absorption
when you walk. So if you take that joint out [by fusing it], then you
take away the shock absorption capability, so you tend to get arthritis
in other joints, which take up the load,” he says.
Recently, Hardin had surgery to remove a disc and fuse
the third and fourth vertebrae in her back. That, a lift in her right
shoe, new AFOs and a substantial weight loss have, she says, restored
her mobility and relieved her pain. She believes if her leg length difference
had been identified earlier, she might have been spared at least some
of the pain she’s endured over the years.
Meehan says he tries to avoid triple arthrodesis procedures
unless a severe deformity is already causing arthritis in the foot joints.
“It definitely holds the deformity in place,” Meehan says of this fusion
surgery. “It provides you excellent correction. There’s no doubt about
that. And it’s relatively easy to do.” But most of the time, it’s less
than ideal.
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The Achilles tendon and plantar fascia often tighten up and can be surgically released. Tendons can be transferred to new positions, such as from the inside to the outside or top of the foot. |
Moving Tendons, Cutting Bones
“The big move among the foot surgeons is to do osteotomies,
which are cuts in the bone to put the bones in a better position, to
reshape the bones, rather than doing fusions, which take motion away
and don’t hold up over time,” Meehan says. (Toes, however, may need
to be fused.)
“Sometimes the problem can be as simple as a tight heel
cord — Achilles tendon — that needs to be released,” he says.
A band of connective tissue (fascia) that runs from
the heel bone to the ball of the foot on the sole (plantar surface)
often tightens up as well. A plantar fascia release loosens this connective
tissue.
When deformity is involved, Meehan says, “you can do
tendon transfers, using what good motor strength they have left and
moving it to an area where there’s a deficiency.
“Typically, they have a very strong posterior [back]
tendon on the inside of the foot, and typically that’s one of the strong
de-forming forces. So we try and release that from the inside and move
it to the outside of their ankle, to work in an area where they were
strength-deficient.” Tendons can also be transferred to the top of the
foot to help with lifting it during walking.
About half the time, Meehan says, muscles (which are
attached to bones via tendons) retrain themselves to work in a new position.
The rest of the time, a transferred muscle simply acts like a piece
of rope holding the foot in place.
The procedure “redistributes the forces on the foot
and puts the foot in a better position, so functionally you’re better
off,” he says.
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Neurologist Michael Shy examines Justin Wilton, 6, who may have CMT. A diagnostic workup for this disorder generally includes a careful family history, a physical exam, measurements of the speed and intensity of nerve impulses traveling between the spinal cord and muscles, and DNA testing. |
Since 1998, Diane Lareau has had tendon transfers on
both feet, as well as procedures to release her tight Achilles tendons,
remove bony protrusions from each foot, straighten her toes and cut
the tendons underneath them.
After her surgeries, Lareau was able to walk well with
AFOs and New Balance shoes. After trying all kinds of expensive compression
and moisture-removing stockings, she says, “When it comes down to it,
men’s tube socks work wonderfully. You turn them inside out so the seam
doesn’t wreck your toes.”
She compensates for being unable to walk very far by
doing yoga for her lower body and a regular gym workout for her upper
body, which isn’t as much affected by her CMT.
“The thinner you are the better your legs are. And that’s
the only reason I have the will power to stay thin.”
Faulty Wiring - What is CMT?
It’s been called everything from “shark’s
tooth disease” to “charcoal tooth disease,” and it’s usually
(and understandably) referred to by its acronym, CMT. But
Charcot-Marie-Tooth disease is actually a fairly common
nerve disorder, with an uncommon name.
Like many diseases lacking a clear cause,
CMT was originally named for three doctors who first described
it. In 1886, Jean-Martin Charcot and Pierre Marie in France
and Howard Henry Tooth in England identified what they thought,
erroneously, was a spinal cord disease.
We now know that CMT is a genetic disease
of the peripheral nerve fibers, long “wires” that bundle
together to form cablelike structures, or nerves, that run
between the spinal cord and the periph-ery (outside edges)
of the body. The motor nerves carry signals that cause muscles
to move, and the sensory nerves send signals back to the
cord that convey pain, temperature, vibration and other
sensations.
CMT affects some 30 people per 100,000.
Since the early 1990s, more than 20 genes that, when flawed,
can cause CMT, have been identified. Some of these genes
are needed in the nerve fibers, while others are needed
to form and maintain myelin, the insulating coating around
each fiber.
Either way, the symptoms are similar: mild
to severe weakness, especially in the hands and feet, often
accompanied by mild to moderate loss of sensation and less
often by burning or tingling pain in those areas, beginning
in childhood or adolescence. |
Dos and Dont's of CMT-Affected
Feet
Protect your feet from blisters and cuts. Examine your feet frequently for injuries if
you’ve lost sensation, and don’t wear shoes or orthotics that rub. Wounds that aren’t
healing need prompt attention.
- Avoid scalding yourself. If you lack sensation in your feet, test the bath water with
another part of your body.
- Avoid broken bones, which can complicate matters. If you’re falling more than once
a month, rethink how you’re managing your foot problems.
- Work with specialists who understand CMT, with its unique combination of weakness,
loss of sensation, oddly shaped feet and progressive course.
Sources: Robert Meehan, orthopedic surgeon, and Michael Shy, neurologist, Wayne State University, Detroit |
Dos and Don'ts When Considering
Foot Surgery
Get first and second opinions from qualified
professionals. Talk to your MDA clinic physician, and/or
contact the American Orthopaedic Foot & Ankle Society (www.aofas.org,
[800] 235-4855) for a referral.
- Prepare yourself for a six- to nine-month process for
a major foot reconstruction, including a hospital stay,
casting and physical therapy. You won’t be able to bear
weight on the reconstructed foot for about six to eight
weeks.
- Don’t plan to have both feet operated on at the same
time unless you know you’re going to have a lot of reliable
help at home.
- Don’t count on being brace-free. You may still require
AFOs or foot orthotics after surgery.
Sources: Robert Meehan, orthopedic surgeon, and Michael Shy, neurologist, Wayne State University, Detroit |
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