The functional priorities of a
person with CP are, in order of importance, communication, activities of daily
living, mobility in the environment, and walking. Medical professionals must
remember that the patient and family have only a certain amount of time and
energy to devote to these priorities and to various aspects of treatment.
Gross motor function in CP is
related to the degree of involvement, which in turn is a manifestation of the
site and severity of the central nervous system (C.N.S.) lesion. This primary
injury to the C.N.S. produces positive features such as spasticity,
hyper-reflexia and co-contraction, and negative features including weakness,
loss of selective motor control, sensory deficits and poor balance. Clinicians
have traditionally focused more on the positive features because it is possible
to treat spasticity, but it is the negative features which determine when or if
a child will walk.
The secondary abnormalities are best
characterised as growth disorders. They develop over time in a growing child.
Growth of bone occurs via epiphyseal plates, but it is the joint reaction
forces acting on these bones that determine their ultimate shape. If those
forces are correct, the final shape of the bone will be correct. If the forces
are distorted, the final shape of the bone will be distorted. In conditions
such as spastic diplegia, both remodeling of foetal bone alignment and future
modelling of bone as it grows are abnormal. Hence, deformities such as
increased femoral anteversion, external tibial torsion, talipes equinovalgus
(with mid-foot break) and hip subluxation are common and are called lever arm
disease. Muscles work most efficiently on rigid bony levers, which are in the
line of gait progression. Maldirected or bent levers reduce the effectiveness
of muscle action. The conditions for normal muscle growth, on the other hand,
are regular stretching of relaxed muscle under physiological loading. In
children with CP, the skeletal muscle does not relax during activity because of
spasticity and these children have greatly reduced levels of activity because
of weakness and poor balance. Hence, to an orthopaedic surgeon, CP is
essentially a 'short muscle disease.'
Tertiary abnormalities are those
compensations that the individual uses to circumvent the primary and secondary
abnormalities of gait. An example is circumduction gait in co-spasticity of
hamstrings and rectus femoris, caused by abduction of hips in order to clear
the ground. These coping responses must be carefully identified and left alone.
The secondary abnormalities are amenable to treatment, whereas, with the
exception of spasticity, the primary abnormalities are difficult to alter.
Hence, the basis of treatment of CP
lies in analysing the pathology, and determining which portions of it can be
corrected and which cannot. The following modalities are attempted to treat
inadequate muscle growth: passive stretch, night splinting, physical therapy,
botulinum toxin injections, phenol/alcohol injections, and orthopaedic surgery
and / or spasticity reduction. For treatment of spasticity in children younger
than 4 years and adolescents in the midst of their growth spurt, physical
therapy, inhibitory casts, orthotics, or botulinum toxin injections are
preferred. Global spasticity management is the choice between 4 to 7 years.
Selective Dorsal Rhizotomy (SDR) may be employed for pure spasticity, while
mixed patterns and spasticity not fulfilling the selection criteria of SDR may
respond to Intrathecal Baclofen (ITB).
Contractures and lever arm disease
can be corrected only by orthopaedic surgery, but minor deformities may be
managed by bracing. Extrapyramidal symptoms, deficient selective motor control
and abnormal balance mechanisms are presently incurable and are the major
limiting factors in management.
Many of the treatments introduced
for spasticity and other aspects of CP were inadequately evaluated when first
introduced and have become enshrined in clinical practice without benefit of
acceptable evidence of efficacy and effectiveness. Over the last 15 years,
valid and reliable outcome measures have been developed for many relevant aspects
of CP ranging from electomechanical torque measures of spasticity and
instrumented gait analysis and energy assessment to measures of functional
ability and quality of life.
Oral muscle relaxants
·
The benefits of drugs like Baclofen
are severely limited by side effects ( drowsiness, unsteadiness or short-term
memory deficit) when administered orally.
·
The poor lipid solubility means that
the drug reaches the target tissue in very low concentrations.
Phenol (3–7%)&
Alcohol (45–100%)
·
Produce selective denervation when
injected into motor nerves or muscles
·
Because diffusion of both is
limited, the area of effective denervation extends just a few millimetres from
the injection site
·
Duration of denervation: 3–6 months
(alcohol), 4–8 months (phenol)
·
Only for motor nerves such as the
obturator nerve and musculocutaneous nerve
·
Rarely used these days
·
Side effects: pain on injection,
non-selective protein denaturation, possible permanent muscle fibrosis,
dysaesthesias lasting for several weeks
Botulinum Toxin-A
injection
Botulinum toxin injections cause a
focal, dose-dependant, reversible chemodenervation of muscle. It is sometimes
used to buy time in a child deemed too young for surgery (2-4 years) and works
best for localised Gastrocnemius spasticity.
Problems:
·
Expensive
·
Temporary (lasting about 3-6 months)
·
Can only delay (and not usually
prevent) SEMLARASS
·
Ineffective in the presence of
contractures or lever arm disease (femoral/tibial torsion, planovalgus feet,
hip subluxation/dislocation)
·
Reported complications: Muscle
soreness, pain on injection, rash, fatigue, excessive weakness, Influenza-like
symptoms, infection, allergic reaction, Subacromial Impingement Syndrome,
Mediastinitis, Rapid Osteoporosis
·
Pathetic quality of life: stress of
repeated injections, plasters and physiotherapy throughout childhood
·
Antibody formation correlated with
secondary nonresponse
·
High Discontinuation Rates: 76%
after an initially good response according to a study in the west, where
finance was not a consideration
Recent Concerns
·
Toxin acts by weakening muscle and
not by addressing spasticity
·
Long term deleterious effects on
muscle growth and function
Dangerous complications reported
recently leading to FDA issuing a warning in February 2008 against its use in
CP
·
Permanent paralysis
·
Respiratory paralysis and dysphagia
·
Generalised muscle weakness
·
Death
Occupational /
Physical Therapy
OT focuses on the development of
skills necessary for the performance of activities of daily living. These
include play, self-care activities such as dressing, grooming and feeding, and
fine motor tasks such as drawing and writing. OT also addresses cognitive and
perceptual disabilities, especially in the visual-motor area. Another aspect of
OT is the adaptation of equipment and seating to allow better upper extremity
use and to promote functional independence. Neurodevelopmental Therapy and
Sensory Integration are specialized techniques used by the therapists to
achieve these goals. However, the latest policy statement from the American
Academy of Cerebral Palsy & Developmental Medicine (AACP&DM), in 2001,
concludes that the long-term benefits of therapy are marginal and not
measurable. Except for an immediate improvement in the range of motion of
joints, no other functional parameters showed any long-term improvement. A
child with mild CP shows improvement with therapy, whereas the more severe
cases progressively develop contractures and lever arm disease around the age
of 4-7 years, after which no further improvement occurs with continuing
therapy.
Orthosis
The traditional metal and leather
caliper (HKAFO) has no place in the modern management of CP. Newer lightweight,
thermoplastic materials and the use of orthoses only below the knee is the
order of the day. A functional and dynamic design like articulated ankle foot
orthosis (A.F.O.), ground reaction A.F.O. or posterior leaf spring A.F.O. is
usually preferred to solid A.F.O. in ambulatory children.
Selective Dorsal
Rhizotomy
This neurosurgical operation
involves a laminoplasty from L1 to S1 and section of 20% to 40% of the dorsal
nerve rootlets.
Selection criteria:
·
Pure spasticity
·
Good selective motor control
·
Adequate underlying muscle strength
·
Age 4 years to 7 years
·
Diagnosis of spastic diplegia due to
prematurity
Problems:
·
Adverse long-term effects (sensory
disturbance, bladder dysfunction, scoliosis, lordosis, hip dislocations and
foot deformities)
·
Validity of the root tissue
selection process is questionable
·
Uncontrolled clinical results have
not been replicated by controlled trials
·
L oss of antigravity stability and
worsening of motor function
·
Cannot be used in children with
contractures and lever arm disease or upper limb involvement
·
Over 70% will still need Orthopaedic
Surgery. SDR frequently accelerates the need for Orthopaedic Surgery
·
Irreversible
·
The same holds good for other
neurosurgical procedures, e.g., neurectomies and fasciculotomies
Intrathecal Baclofen
An implanted, battery-driven,
microprocessor-controlled pump administers small quantities of Baclofen into
the subarachnoid space, and has a role in severe spastic quadriplegia.
Problems:
·
Exorbitantly expensive
·
Invasive and associated with
life-threatening complications, e.g., neurological injuries due to catheter tip
dislodgement, intradural infection and fibrosis , etc.
·
Rapidly progressing scoliosis
·
R eplacement of tube and refilling
of pump require multiple risky operations
·
A cts predominantly on the lower
limbs
Conventional
Orthopaedic Surgery
Problems:
·
Lengthening of monoarticular
(muscles that cross only one joint) muscles or tendons (adductor brevis,
iliopsoas, tendoachilles) leading to loss of antigravity action and severe
weakness
·
Over lengthening of tendons common
·
Muscle transfers (Eggers) leading to
reverse deformity, e.g., genu recurvatum
·
Does not help the severely involved:
quadriplegics, athetoid, dystonia
·
Joint fusions (Grice fusion):
degeneration of surrounding joints
·
Lever arm dysfunction rarely
corrected simultaneously or early enough: recurrence of contractures
·
Cannot control spasticity, produce
reciprocal movements to facilitate antigravity muscles, and improve functional
skills and voluntary movement of the hand
What's new in the management of CP?
SEMLARASS or Single Event Multilevel
Lever Arm Restoration and Anti Spasticity Surgery include the following
components:
·
Single
event : all surgeries are usually
completed under a single anaesthetic, requiring only one hospital admission and
one period of rehabilitation
·
Multilevel
: all the affected regions and all
orthopaedic deformities (soft tissue and bony) are corrected simultaneously in
view of interdependence of joints
·
Lever arm
restoration : simultaneous correction of hip
subluxation, femoral anteversion, tibial torsion, hindfoot valgus to improve
the direction of pull of muscles
·
Anti
spasticity : myofascial surgical releases to
reduce spasticity
SEMLARASS was conceptualised by Dr.
Deepak Sharan at RECOUP, Bangalore , India , in 2000.
The unique features of SEMLARASS
include:
·
Operating between the ages of 4
years to 8 years (preferably), to avoid joint decompensation and over
lengthening of tendons that happen due to continued usage of deformed joints.
We consider modalities used to postpone SEMLARASS like Botulinum Toxin, Casting
or SDR harmful to the child's eventual outcome because of development of over
lengthened tendons and joint decompensation.
·
Minimally invasive procedures using
image intensifier that do not require large skin incisions and consequent risk
of blood loss and infection
·
Use of External Fixators that do not
require a second operation for removal
·
All bony operations done to restore
deformed lever arms are extra-articular (not involving joints) to allow for the
maximum growth potential of children's bones
·
Simultaneous lever arm restoration
is essential for spasticity and contracture correction as well as to reduce
chances of recurrence of deformities and repeat surgery at a later stage
·
Tendon lengthening is avoided to reduce
weakness
·
The surgery is followed by a
supervised and intensive protocol based rehabilitation developed at RECOUP.
SEMLARASS draws its origin from 2
prevalent concepts in the surgical treatment of CP:
1.
Orthopaedic Selective Spasticity
Control Surgery (OSSCS), developed by Dr. Takashi Matsuo ( Tokyo , Japan )
based on the principle that multiarticular muscles, which have less antigravity
activity, are hyperactive in CP. Therefore, spasticity and athetotic movements
can be controlled by releasing them selectively. The monoarticular muscles,
which have antigravity activity and are responsible for maintaining an upright
posture, are carefully preserved. Hence, there is no loss of antigravity
activity or muscle weakness and no loss of sensation and stereognosis.
2.
Correction of lever arm dysfunction
(e.g., hip subluxation, increased femoral anteversion, tibial torsion and
hindfoot valgus) as proposed by Dr. James Gage from Minnesota , USA .
In the majority of CP patients,
SEMLARASS is necessary to correct contractures, correct bony deformities, and
re-balance abnormal muscle forces producing gait deviations.
SEMLARASS offers correction of all orthopaedic deformities (soft
tissue and bony) in one session, requiring only one hospital admission and one
period of rehabilitation. OSSCS is based on the concept that the
multiarticular muscles, which have less antigravity activity, are hyperactive
in CP. Therefore, spasticity and athetotic movements can be controlled by
releasing them selectively. The monoarticular muscles, which have antigravity
activity and are responsible for maintaining an upright posture, are carefully
preserved. Hence, there is no loss of antigravity activity (muscle weakness)
and no loss of sensation and stereognosis. There is also no increase in the
occurrence of dislocations and deformities. With the availability of OSSCS, w e
can now control spasticity of the neck, shoulder, elbow, forearm, wrist,
fingers, thumb, extensor pattern of the trunk, paralytic scoliosis, hip, knee
and foot, and therefore can facilitate the stability of the neck, trunk,
shoulder and elbow and of the lower extremities, and can activate skills of the
hand. Control of the abnormal postural reflex can be accomplished and
alternation such as reciprocal movement and cross-patterned movement of the
extremities is also facilitated. More stable postures such as sitting and
standing, and stable transfers such as crawling and gait, by facilitating
activity of the antigravity muscles, can be achieved.
SEMLARASS avoids most of the
problems associated with SDR, ITB and Conventional Orthopaedic Surgery. The
advantages of performing all the procedures under a single anaesthetic include
avoidance of additional pain and inconvenience, repeated costly
hospitalisations, and need for the child to complete more than one
postoperative rehabilitation programme. This also eliminates multiple periods
of functional regression that normally follow each surgical procedure. Precise
correction, stable fixation and early mobilisation are essential for a good
outcome.
We have been performing SEMLARASS
since the year 2000 (over 10,000 surgeries in 600 patients from all over India
and other countries, including over 100 patients from Kerala): Spastic diplegia
65%; Spastic hemiplegia 20%; Spastic quadriplegia 15%; Spastic or mixed 75%;
athetoid 20%; dystonia 5%. Follow up 1 year to 8 years (mean 4.5 years).
Improved functional results were recorded in almost all patients using
Instrumented Computerised Gait Analysis (available at RECOUP, Bangalore since
2007) , video gait recording, observational gait analysis, Gross Motor Function
Classification System and other functional scales. Several children have now
achieved near normalcy of gait. Video recordings before and after surgery, and
an opportunity to meet/speak to parents of operated children are routinely made
available to parents when they are considering this surgery.
With SEMLARASS, even selected cases
of spastic quadriplegia and athetoid CP can be improved functionally.
Traditionally, these children have been bed-bound with an abysmal quality of
life. After SEMLARASS, significant improvements may be noted in head control,
sitting and standing balance, and limited ambulation. Mental retardation is not
a contraindication for surgery. A major advantage of SEMLARASS that has been
noted is an all round acceleration of other functions thereafter, e.g.,
learning, speech, behaviour, etc. Decreased spasticity allows the child to have
greater range of motion, less spastic response to stretch, and better potential
to develop and use voluntary activity during gait. Physical therapy for
strengthening muscles is more effective once spasticity is reduced. Functional
strength training (Suspended treadmill training, suspended bicycle training,
therapeutic swimming and horse back riding (hippotherapy) are useful modalities
in this situation (all are available exclusively in Bangalore ). The
traditional view was that muscle strengthening was neither possible nor
desirable in CP because it might increase spasticity. Recent research has shown
that muscle strength can be reliably measured in children with CP and that
those who participate in strengthening programmes demonstrate increases in
muscle power and improvements in function.
The postoperative rehabilitation
following SEMLARASS is intensive and protocol based, and requires dedicated and
skilled physical therapy for at least 2 years. Functional improvement is slow
and steady and can continue for 2 years or more.
Ideal age for surgery
It is very important to emphasise
the ideal age for surgery: 4-8 years. The child develops a mature gait pattern
by the age of 4 or 5 years and is better able to cooperate with the intensive
post-operative physiotherapy programme. Once this window of opportunity is lost
(usually due to reluctance of physiotherapists to let go or the insistence of
the family in exploring non-operative options at any cost) and complex
decompensated joint pathology has developed, the results of operation are less
gratifying, though functional improvements still occur in older children and
adults. Unstable lever arm disease must be operated irrespective of age if
there is to be any hope of preserving ambulation. We have seen cases of
ruptured tendoachilles due to forcible muscle stretching by physiotherapists in
the presence of contractures, necessitating an emergency multi level SEMLARASS!
A common misconception is that as long as the child is somehow able to walk,
surgery should be avoided. The problem is that co-spasticity of muscles acting
across the joints and the development of deformities makes the gait laborious,
energy consuming and inefficient. After SEMLARASS, studies using instrumented
gait analysis have shown significant improvement in gait, energy efficiency,
appearance, and function.
Conclusion
Currently, a well-planned and
executed SEMLARASS , in the context of a multi-disciplinary team, provides the
child with CP with the only hope for a dramatic, predictable and lasting
functional improvement. Indeed, a programme for treating CP that fails to make
SEMLARASS available to its patients deprives them of one of the most effective
treatment aids. However, this is like a double-edged sword: SEMLARASS should be
done only at tertiary level centers by highly experienced surgeons who have
received the appropriate training in centers of excellence.
Comments
Post a Comment