2.1 Managing Symptoms of PSP: Movement Problems This Help Sheet gives further information about the movement-related
symptoms of Progressive Supranuclear Palsy (PSP for short), such as
stiffness, muscle cramps, walking and fal ing. It also suggests therapies,
treatments and strategies for managing these symptoms. The
information here is presented as a guide; it is important to discuss al
symptoms with your neurologist and other health professionals.
PSP is a rare neurological condition affecting the parts of the brain that
control walking, eye movements, balance, speech and swallowing. PSP
has a wide range of symptoms, but few people experience them all and
symptoms vary from person to person. It is a progressive condition,
meaning that the symptoms tend to worsen over time. However, the
severity and rate of symptom progression varies widely.
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Difficulties with movement and balance are a common feature of PSP.
The problems are caused by a breakdown in messages between the
brain and the body. The problem is not with the muscles and joints
themselves, although as movement becomes more and more difficult
the muscles may stiffen due to lack of movement.
Exercise – Keep moving to keep moving
Regular exercise helps to keep the muscles supple and the joints
moving. Daily walking or swimming are good forms of exercise for
people with PSP. Other forms of gentle exercise can also be very helpful
in managing movement-related symptoms, including Tai Chi and
strength-training programs. Be aware, however, that advancing balance
problems can make these exercises difficult or dangerous. Even when
walking or standing becomes too difficult to manage, it is important to
keep exercising. To accomplish this there are a series of passive
stretching exercises that can be performed when seated.
Muscle cramps due to stiff muscles and reduced movement can be
Treatments for muscle cramps can include:
• Gentle massage or passive exercise to the affected area. Try
one of the many electric or battery operated massage devices
• Heat packs, such as a ‘Wheat Bag’, which can be heated in
the microwave. Please note: people who are diabetic should
not use heat packs without doctor’s advice.
• Injections of botulinum toxin (Botox ® or Dyspport ®) to
the muscles in an effort to relieve pain and spasm. Botulinum
toxin prevents the muscle from contracting, thereby reducing
muscle spasms. Treatments will probably need to be repeated
every 3 or 4 months. Discuss this with your neurologist.
• Other medications may also be considered by your
Walking difficulties and falls are a common problem for people
with PSP. It is important to minimise falls because they can result in
serious injury, particularly as people with PSP often fal backwards.
Simple strategies you can use to minimise the risk of falls and reduce
• Wearing comfortable, well-fitting flat shoes. A physio-
therapist can advise on the best shoes to wear.
• Removing low objects such as rugs, low coffee tables and
• Repairing loose carpet and uneven or slippery surfaces,
remembering that people with PSP often walk with a shuffle
• Keeping items that are regularly needed close at hand.
• Thinking about different and safer ways of doing things and
considering the consequences before undertaking risky tasks
Services and professionals that can help
The following services and professionals can help minimise movement
problems, maintain safety and maximise independence and quality of
life. Many are provided at a low cost and Medicare now funds a
limited number of visits to an allied health professional such as a
physiotherapist when you are referred by a General Practitioner for
an Enhanced Primary Care Plan. You can find out what services are
available in your area by contacting Parkinson’s Australia.
Physiotherapists can help with:
• Advice on stretches that can help stiff muscles and joints to
• The provision of an exercise program to maintain muscle
• Techniques to make movements more automatic and strategies
to manage movement difficulties, such as turning over in bed.
• Advice for carers on the safest and best way to assist the
person with PSP; for example, safe lifting techniques.
Occupational therapists can help with assessment of the home
environment and advice on equipment and strategies to maximise
Movement Disorder Clinics in some areas provide specialist services
to help manage movement problems such as those caused by PSP and
Equipment and independent living aids are available and in some
cases may help manage movement problems and assist with daily
• Walking frames can help ease walking difficulties and reduce
the risk of falling. Your physiotherapist is the best person to
advise on the type of walking frame suited to your individual
• Wheelchair use can help to increase mobility and maintain
independence. For example, it can be useful when attending a
crowded event. The wheelchair should be individually fitted with
the advice of a physiotherapist or occupational therapist.
• Home safety equipment such as grab-rails, ramps, accessible
toilet and shower facilities and hoists can help to maintain safety
and independence at home. Your occupational therapist can
• Elbow pads and hip or head protectors can provide Help Sheet 2.1
important protection for people with severe balance problems
and protect them from fractures in the event of a fall.
Movement problems
Costs for some of these items may be subsidised for some people. Your
physiotherapist or occupational therapist can advise on available
equipment and help you to obtain what you need.
Independent Living Centres can also provide information and
advice about resources to make every-day living easier. To contact
the Independent Living Centre in your state or territory telephone the
ILC Infoline on 1300 885 886 or visit: www.ilcaustralia.org.au
It can be a good idea to introduce independent living aids before they
are needed, so that both carers and the person with PSP become
Remember: PSP is a progressive condition and symptoms will get worse over time. It is important to plan ahead for future needs, for example, by installing equipment to reduce the risk of falls at home ahead of time rather than waiting until after a serious fall.
Medications to help with movement problems
• Dopamine medications
Dopamine is the brain chemical that is lacking in people who
have Parkinson’s disease. Some medications used to treat
Parkinson’s can help treat some of the movement-related
symptoms of PSP. Unfortunately, dopamine medications do not
work as well in PSP as they do in Parkinson’s because in PSP
dopamine is not the only brain chemical affected.
There are a number of different dopamine medications and
side-effects are common. They can include nausea,
constipation, confusion, hal ucinations, and behavioural
problems such as feeling an uncontrollable need to gamble,
have sex or pursue hobbies. Side effects can usually be
treated. It is important to discuss all symptoms, side-effects
• Amantadine (sold under the brand name Symmetrel) may
be more effective than other dopamine drugs in treating
movement symptoms of PSP because it affects more than just
the dopamine system. Unfortunately the benefits often do not
last longer than a few months. Side effects include dry mouth,
constipation, confusion and swelling of the ankles.
• Antidepressant medications
Some of the movement problems experienced by people with
PSP appear to improve with the use of antidepressant
medications. We do not fully understand the reasons for this;
however, we do know that the improvement in movement is
not related to the medication’s ability to relieve depression.
Side-effects may include constipation, dry mouth, confusion
Treatment found to have no benefit in PSP includes many different
medications, some surgical procedures and Alzheimer’s disease
Remember: treatment options are evolving all of the time and it is important to regularly discuss the latest treatment options with your neurologist. For example, recently co-enzyme Q10 was suggested as a useful agent to reduce disability over the long term. This study was preliminary and further studies are planned.
For further information about living with PSP,
including the full range of PSP Australia Help Sheets,
Help Sheet 2.1 Movement problems
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Management of PDA in RDS In healthy term infants and preterm infants without RDS constriction and closure of the ductus arteriosus is complete within 48 hours of delivery in 90% of cases and in 100% by 96 hours.1,2 Closure is often delayed in preterm infants with RDS and is inversely related to gestational age. In one study 42% of infants < 1000g developed a significant PDA and this dec