NEUROLOGICAL CONDITIONS

ALL CONDITIONS TREATED AT DJD SURGERY

The information outlined below on common neurological conditions is provided as a guide only and it is not intended to be comprehensive. Discussion with Mr Davies is important to answer any questions that you may have. For information about any additional conditions or symptoms not featured within the site, please contact us for more information.

A brain tumour is a growth of cells in the brain that multiplies in an abnormal, uncontrollable way.

Grades and types of brain tumour

Brain tumours are graded according to how fast they grow and how likely they are to grow back after treatment. Grade 1 and 2 tumours are low grade, and grade 3 and 4 tumours are high grade.

There are 2 main types of brain tumours:

  • non-cancerous (benign) brain tumours – these are low grade (grade 1 or 2), which means they grow slowly and are less likely to return after treatment
  • cancerous (malignant) brain tumours – these are high grade (grade 3 or 4) and either start in the brain (primary tumours) or spread into the brain from elsewhere (secondary tumours); they’re more likely to grow back after treatment

Symptoms of a brain tumour

The symptoms of a brain tumour vary depending on the exact part of the brain affected.

Common symptoms include:

  • headaches
  • seizures (fits)
  • persistently feeling sick (nausea), being sick (vomiting) and drowsiness
  • mental or behavioural changes, such as memory problems or changes in personality
  • progressive weakness or paralysis on one side of the body
  • vision or speech problems

Sometimes you may not have any symptoms to begin with, or they may develop very slowly over time.

When to see a GP

See a GP if you have these types of symptoms, particularly if you have a headache that feels different from the type of headache you usually get, or if headaches are getting worse. You may not have a brain tumour, but these types of symptoms should be checked.

If the GP cannot identify a more likely cause of your symptoms, they may refer you to a doctor who specialises in the brain and nervous system (neurologist) for further assessment and tests, such as a brain scan.

Who’s affected

Brain tumours can affect people of any age, including children, although they tend to be more common in older adults. More than 12,000 people are diagnosed with a primary brain tumour in the UK each year, of which about half are cancerous. Many others are diagnosed with a secondary brain tumour.

Causes and risks

The cause of most brain tumours is unknown, but there are several risk factors that may increase your chances of developing a brain tumour.

Risk factors include:

  • age – the risk of getting a brain tumour increases with age (most brain tumours happen in older adults aged 85 to 89), although some types of brain tumour are more common in children
  • radiation – exposure to radiation accounts for a very small number of brain tumours; some types of brain tumours are more common in people who have had radiotherapy, or very rarely, CT scans or X-rays of the head
  • family history and genetic conditions – some genetic conditions are known to increase the risk of getting a brain tumour, including tuberous sclerosis, neurofibromatosis type 1, neurofibromatosis type 2 and Turner syndrome

Treating brain tumours

If you have a brain tumour, your treatment will depend on:

  • the type of tumour
  • where it is in your brain
  • how big it is and how far it’s spread
  • how abnormal the cells are
  • your overall health and fitness

Treatments for brain tumours include:

  • steroids
  • medicines to help with symptoms
  • surgery
  • radiotherapy
  • chemotherapy

After being diagnosed with a brain tumour, steroids may be prescribed to help reduce swelling around the tumour. Other medicines can be used to help with other symptoms of brain tumours, such as anti-epileptic medicines for seizures and painkillers for headaches.

Surgery is often used to remove brain tumours. The aim is to remove as much abnormal tissue as safely as possible. It’s not always possible to remove all of a tumour, so further treatment with radiotherapy or chemotherapy may be needed to treat any abnormal cells left behind.

Treatment for non-cancerous tumours is often successful and a full recovery is possible. Sometimes there’s a small chance the tumour could return, so you may need regular follow-up appointments to monitor this.

Outlook

If you have a brain tumour, your outlook will depend on several factors, including:

  • your age
  • the type of tumour you have
  • where it is in your brain
  • how effective the treatment is
  • your general health

Survival rates are difficult to predict because brain tumours are uncommon and there are many different types. Your doctor will be able to give you more information about your outlook. Generally, around 17 out of every 100 people with a cancerous brain tumour will survive for 5 years or more after being diagnosed.

Cerebrospinal fluid (CSF) disorders encompass a wide variety of conditions. Everyone has CSF; it is mainly produced in the choroid plexus and flows around the sub-arachnoid space surrounding the brain and spinal cord. It then passes through a series of chambers in the brain called ventricles and connecting channels called foramina. We produce about a pint (500ml) of CSF per day but the brain can contain only about 120-150ml. For this reason excess CSF is drained into the bloodstream through a series of valves called the arachnoid villi. The CSF is recycled about three times a day.

CSF helps to protect the brain by cushioning it within the skull, and also serves as a shock absorber for the central nervous system. CSF also circulates nutrients and chemicals from the blood and removes waste products from the brain. CSF leaks, hydrocephalus, Chiari malformation and Syringomyelia fall under the umbrella of CSF disorders.

Hydrocephalus

This happens when the cerebrospinal fluid (CSF) builds up, putting pressure on the brain and leading to damage. This can cause a wide range of symptoms, including headache, blurred vision, sickness and difficulty walking.

There are three main types of hydrocephalus:

  • Congenital Hydrocephalus – This is present at birth and can cause permanent brain damage and long-term mental and physical disabilities. It can be caused by conditions such as spina bifida, or an infection the mother develops during pregnancy, such as mumps or rubella (German measles).
  • Acquired Hydrocephalus – This develops after birth, usually as a result of a serious head injury or following a lesion obstructing the CSF pathways such as a brain tumour.
  • Normal Pressure hydrocephalus (NPH) – a rare illness which usually only develops in people aged over 50. Although it can develop after an injury or a stroke, most of the time the cause is unknown.

Diagnosing hydrocephalus is usually by an MRI or CT scan. Further tests may need to be carried out before Dr Davies can make a diagnosis.

HOW IS HYDROCEPHALUS TREATED?

Hydrocephalus is usually treated with surgery (one of two surgical treatments):

1- SHUNT

The most common treatment for hydrocephalus is the insertion of a shunt, which acts as a drainage system to bypass the patient’s existing CSF absorption mechanisms. It consists of a long, flexible thin tube with a valve that keeps fluid from the brain flowing in the right direction and at the correct rate.

One end of the tubing is usually placed in one of the brain’s ventricles (this is a CSF containing chamber in the brain). The tubing is then tunneled under the skin to another part of the body where the excess cerebrospinal fluid can be more easily absorbed — this is usually the abdomen, but also be the heart atrium or chest.

People who have hydrocephalus usually need a shunt system for the rest of their lives, and regular monitoring is required.

2- ENDOSCOPIC THIRD VENTRICULOSTOMY

Endoscopic third ventriculostomy is a surgical keyhole procedure that can be used for some patients. This procedure aims to internally bypass the existing CSF pathway and no implantable device is needed. In the procedure, a small video camera is used for direct visualisation inside the brain. A hole in the bottom of one of the ventricles or between the ventricles to enable cerebrospinal fluid to flow out of the brain, circulate and absorb.

Chiari Malformation

Chiari Malformation (CM) also known as Hindbrain Hernia is a rare condition involving the base of the brain and spinal cord. In this condition the cerebellar tonsils of the brain descend through an opening in the base of the skull (named the Foramen Magnum) into what should be a space alongside the spinal cord. This can cause compression of the brain stem and disruption of the flow of cerebrospinal fluid (CSF) at the top of the spinal canal. This can cause a number of symptoms: pain and tingling in the limbs, dizziness, nausea, balance problems, visual disturbances, problems swallowing, pressure headaches, which worsen when straining, laughing or coughing.

Chiari Malformation is diagnosed by an MRI scan.

HOW IS CHIARI MALFORMATION TREATED?

A decompression surgery may be offered to try to relieve symptoms and stop the condition progressing.

Before any surgery is undertaken, detailed discussions need to take place between the patient and the neurosurgeon, as to the potential benefits of surgery as well as the inconveniences, discomforts and risks that go with an operation on the brain or spinal cord.

Syringomyelia

Syringomyelia is a disorder affecting the nervous system where fluid-filled cavities develop inside the spinal cord. The spinal cord is normally a solid structure, which passes down the back inside the spinal canal. It connects the brain to the rest of the body, passing signals to and fro, enabling an individual to move his or her limbs at will, to feel objects and to control various bodily functions.

Within the spinal canal, the spinal cord is bathed with CSF. The fluid from which Syringomyelia cavities are formed is identical to CSF.

Normally CSF flowing in the spinal canal communicates freely with CSF circulating inside the head but when CSF is trapped inside the spinal canal some of it begins to accumulate within the substance of the spinal cord.

WHAT CAUSES SYRINGOMYELIA?

Next to Chiari Malfromation, the most common cause of Syringomyelia is spinal injury. A minority of victims of severe spinal cord trauma, who are already severely disabled as a result of their original injury, go on to develop additional problems as a result of Syringomyelia. Scar tissue within the spinal canal, developing as a consequence of the initial injury, obstructs CSF movement causing, once again, fluid to accumulate within the substance of the spinal cord.

There are other causes of Syringomyelia beyond the scope of these pages.

HOW IS SYRINGOMYELIA DIAGNOSED?

Patients who have Syringomyelia present with a variety of symptoms ranging from neck and arm pain through to fairly severe disability, with muscle weakness and paralysis. Fortunately nowadays, most cases of Syringomyelia are detected at an early stage before major disability develops.

Any of the symptoms of Syringomyelia can have other causes. Indeed, it is much more likely that somebody presenting with, say, neck and arm pain, will have a more common disorder and not Syringomyelia.

It is only when more common diseases are excluded that Syringomyelia may be considered as a diagnosis. In most cases the diagnosis of Syringomyelia is made by a specialist, usually a Neurologist.

Once the diagnosis of Syringomyelia is suspected, it is readily confirmed by an MRI scan.

HOW IS SRINGOMYELIA TREATED?

In many cases of Syringomyelia all that a patient needs is an explanation and reassurance, together with periodic review by a specialist.

The symptoms arising from Syringomyelia can be treated with drugs, other measures, or simply tolerated.

In some instances, however, if the cavity in the spinal cord is enlarging and threatens to cause significant disability, there may be a place for surgical intervention. In these circumstances the services of a neurosurgeon may be required. Before any surgery is undertaken, detailed discussions need to take place between the patient and the neurosurgeon, as to the potential benefits of surgery as well as the inconveniences, discomforts and risks that go with an operation on the brain or spinal cord.

Chiari Malformation (CM) also known as Hindbrain Hernia is a rare condition involving the base of the brain and spinal cord. In this condition the cerebellar tonsils of the brain descend through an opening in the base of the skull (named the Foramen Magnum) into what should be a space alongside the spinal cord. This can cause compression of the brain stem and disruption of the flow of cerebrospinal fluid (CSF) at the top of the spinal canal. This can cause a number of symptoms: pain and tingling in the limbs, dizziness, nausea, balance problems, visual disturbances, problems swallowing, pressure headaches, which worsen when straining, laughing or coughing.

Chiari Malformation is diagnosed by an MRI scan.

How is Chiari Malformation treated?

A decompression surgery may be offered to try to relieve symptoms and stop the condition progressing.

Before any surgery is undertaken, detailed discussions need to take place between the patient and the neurosurgeon, as to the potential benefits of surgery as well as the inconveniences, discomforts and risks that go with an operation on the brain or spinal cord.

Trigeminal neuralgia is sudden, severe facial pain. It’s often described as a sharp shooting pain or like having an electric shock in the jaw, teeth or gums. It usually happens in short, unpredictable attacks that can last from a few seconds to about 2 minutes. The attacks stop as suddenly as they start.

In most cases, trigeminal neuralgia affects just one side of the face, with the pain usually felt in the lower part of the face. Very occasionally the pain can affect both sides of the face, although not usually at the same time.

People with the condition may experience attacks of pain regularly for days, weeks or months at a time. In severe cases attacks may happen hundreds of times a day. It’s possible for the pain to improve or even disappear altogether for several months or years at a time (remission), although these periods tend to get shorter with time. Some people may then develop a more continuous aching, throbbing or burning sensation, sometimes accompanied by the sharp attacks.

Living with trigeminal neuralgia can be very difficult. It can have a significant impact on a person’s quality of life, resulting in problems such as weight loss, isolation and depression.

What Causes Trigeminal Neuralgia

Trigeminal neuralgia is usually caused by compression of the trigeminal nerve. This is the nerve inside the skull that transmits sensations of pain and touch from your face, teeth and mouth to your brain.

The compression of the trigeminal nerve is usually caused by a nearby blood vessel pressing on part of the nerve inside the skull.

Trigeminal neuralgia can also happen when the trigeminal nerve is damaged by another medical condition, such as multiple sclerosis (MS) or a tumour.

The attacks of pain are usually brought on by activities that involve lightly touching the face, such as washing, eating and brushing the teeth, but they can also be triggered by wind – even a slight breeze or air conditioning – or movement of the face or head. Sometimes the pain can happen without a trigger.

Who’s affected?

It’s not clear how many people are affected by trigeminal neuralgia, but it’s thought to be rare.

Trigeminal neuralgia affects more women than men, and it usually starts between the ages of 50 and 60. It’s rare in adults younger than 40.

Treating Trigeminal neuralgia

Trigeminal neuralgia is usually a long-term condition and the periods of remission often get shorter over time. However, the treatments available do help most cases to some degree.

An anticonvulsant medicine called carbamazepine, which is often used to treat epilepsy, is the first treatment usually recommended to treat trigeminal neuralgia. Carbamazepine can relieve nerve pain by slowing down electrical impulses in the nerves and reducing their ability to transmit pain messages.

Carbamazepine needs to be taken several times a day to be effective, with the dose gradually increased over the course of a few days or weeks so high enough levels of the medicine can build up in your bloodstream.

Unless your pain becomes much better, or disappears, the medicine is usually continued for as long as necessary, which could be for many years.

If you’re entering a period of remission, where your pain goes away, stopping carbamazepine should always be done slowly, over days or weeks, unless a doctor tells you otherwise.

If this medicine does not help you, causes too many side effects, or you’re unable to take it, you may be referred to a specialist to discuss alternative medicines or surgical procedures that may help.

There are a number of minor surgical procedures that can be used to treat trigeminal neuralgia – usually by damaging the nerve to stop it sending pain signals – but these are generally only effective for a few years.

Alternatively, your specialist may recommend having surgery to open your skull and move any blood vessels that are compressing the trigeminal nerve. Research suggests this operation offers the best results for long-term pain relief, but it’s a major operation and carries a risk of potentially serious complications, such as hearing loss, facial numbness or, very rarely, a stroke.

Haemangioblastomas are rare non cancerous (benign) brain tumours. They start in the cells that line the blood vessels in the brain, spinal cord and brain stem. They usually grow slowly over some years. Most haemangioblastomas start in the back of the brain (cerebellum).

Haemangioblastomas don’t usually spread to other parts of the brain. The symptoms you have depend on where the tumour is in the brain or spinal cord. Symptoms might include:

  • problems with walking, balance, speech and coordination
  • a build up of brain fluid (cerebrospinal fluid) which can cause headaches and feeling sick

Some haemangioblastomas happen because of a rare inherited syndrome called von Hippel-Lindau syndrome. People with this syndrome have a higher risk of developing different types of tumours, including haemangioblastoma.

How Common is it?

Haemangioblastomas are rare tumours. They are a type of tumour called haemangiomas. Around 1 out of every 100 brain tumours (around 1%) diagnosed are haemangiomas. Around 12,300 people are diagnosed with a brain tumour in the UK each year. This includes tumours in other parts of the central nervous system as well.

How is it diagnosed?

To find out what is causing your symptoms your doctor will arrange for you to have some tests. The tests you might have include:

  • MRI scan or CT scan
  • blood tests
  • a test of your neurological system (neurological examination)
  • a scan to look at the blood vessels in the brain (brain angiogram)
  • a biopsy

As well as finding out whether you have a tumour, the tests check the size of the tumour and its location. This helps your doctor plan your treatment.

Treating Haemangioblastomas

The treatment you have depends on:

  • the size of your tumour and whether it is growing
  • the symptoms you have
  • your age
  • your quality of life

Treatment might be monitoring, surgery or radiotherapy. The team caring for you will talk to you about your treatment.

MONITORING

You might not need treatment straight away if you have a very small haemangioblastoma which isn’t growing. And if you don’t have symptoms. If this is the case, your doctors may recommend monitoring the tumour with regular MRI scans. This is called watchful waiting or active surveillance.

SURGERY

Surgery is the main treatment for haemangioblastoma. A brain specialist surgeon (neurosurgeon) removes all the tumour or just a part. This depends on where the tumour is.

You might have side effects after the operation. The side effects include:

  • bleeding in the brain
  • infection in the membranes that surround the brain (meningitis)

RADIOTHERAPY

You might have radiotherapy if:

  • you can’t have surgery for any reason
  • your haemangioblastoma has come back after surgery
  • doctors couldn’t remove all the tumour during the operation

You might have a type of radiotherapy called stereotactic radiotherapy or radiosurgery. Both treatments target high doses of radiotherapy to the tumour.

Coping with haemangioblastoma

Coping with a diagnosis of a brain tumour can be difficult, both practically and emotionally. It can be especially difficult when you have a rare tumour. Being well informed about the type of tumour you have, and its treatment can make it easier to cope.

Hydrocephalus happens when the cerebrospinal fluid (CSF) builds up, putting pressure on the brain and leading to damage. This can cause a wide range of symptoms, including headache, blurred vision, sickness and difficulty walking.

There are three main types of hydrocephalus:

  • Congenital Hydrocephalus – This is present at birth and can cause permanent brain damage and long-term mental and physical disabilities. It can be caused by conditions such as spina bifida, or an infection the mother develops during pregnancy, such as mumps or rubella (German measles).
  • Acquired Hydrocephalus – This develops after birth, usually as a result of a serious head injury or following a lesion obstructing the CSF pathways such as a brain tumour.
  • Normal Pressure hydrocephalus (NPH) – a rare illness which usually only develops in people aged over 50. Although it can develop after an injury or a stroke, most of the time the cause is unknown.

Diagnosing hydrocephalus is usually by an MRI or CT scan. Further tests may need to be carried out before Dr Davies can make a diagnosis.

How is Hydrocephalus treated?

Hydrocephalus is usually treated with surgery (one of two surgical treatments):

1- SHUNT

The most common treatment for hydrocephalus is the insertion of a shunt, which acts as a drainage system to bypass the patient’s existing CSF absorption mechanisms. It consists of a long, flexible thin tube with a valve that keeps fluid from the brain flowing in the right direction and at the correct rate.

One end of the tubing is usually placed in one of the brain’s ventricles (this is a CSF containing chamber in the brain). The tubing is then tunneled under the skin to another part of the body where the excess cerebrospinal fluid can be more easily absorbed — this is usually the abdomen, but also be the heart atrium or chest.

People who have hydrocephalus usually need a shunt system for the rest of their lives, and regular monitoring is required.

2- ENDOSCOPIC THIRD VENTRICULOSTOMY

Endoscopic third ventriculostomy is a surgical keyhole procedure that can be used for some patients. This procedure aims to internally bypass the existing CSF pathway and no implantable device is needed. In the procedure, a small video camera is used for direct visualisation inside the brain. A hole in the bottom of one of the ventricles or between the ventricles to enable cerebrospinal fluid to flow out of the brain, circulate and absorb.

Anoxic brain injuries and hypoxic brain injuries are different types of injuries according to how much oxygen deprivation the brain experienced. Unlike a traumatic brain injury that is caused by blunt force trauma, these types of brain injuries are caused by a lack of oxygen.

An anoxic brain injury occurs when oxygen flow to the brain is completely cut off. When this happens, brain cell death will begin around four minutes from the time of deprivation.

A hypoxic brain injury is when the flow of oxygen to the brain is restricted. When the brain cannot get enough oxygen, brain cells begin to die gradually, ultimately leading to impairment.

What are the causes

Oxygen deprivation is the cause for both types of brain injuries. Lack of oxygen to the brain can happen for a variety of reasons. A stroke is a common cause, however, oxygen deprivation can also occur if the lungs themselves experience trauma and are not able to take in oxygen properly or if oxygen flow within the body is impaired for any reason.

Types of oxygen restrictions that cause brain injury include:

  • Anemic anoxia: occurs when blood cannot carry enough oxygen or there might not be enough blood in the body to support the oxygen needs of the brain.
  • Hypoxic ischemic injury: is when blood that carries oxygen to the brain cannot reach the brain. This can happen after strokes or pulmonary conditions such as a heart attack or cardiac arrhythmia.
  • Toxic anoxia: this occurs when chemicals or poisons hinder the brain from getting oxygen from blood cells.
  • Anoxic anoxia: a lack of oxygen in the air that results in suffocation.

In other words, if you experience a trauma that affects your body’s ability to take in and/or distribute oxygen, it can have profound effects on the brain as well, even if the initial problem did not originate in the brain.

Because each injury is unique, and the inciting incident may not appear to involve the brain at first, it can be helpful to know what the symptoms of these types of injuries can look like.

Symptoms of Anoxic and Hypoxic Brain Injuries

In many cases, people experiencing oxygen deprivation will lose consciousness initially. If they recover consciousness but don’t receive immediate treatment, they may notice both physical and behavioral symptoms:

Physical impairments:

  • Headache
  • Vision issues
  • Changes in sensory perception
  • Changes in sleep patterns
  • Apraxia (motor skill impairment)
  • Aphasia (difficulty speaking and forming words)
  • Seizure
  • Lack of bowel and bladder control
  • Memory problems

Behavioral changes:

  • Personality changes
  • Depression
  • Poor concentration
  • Mood swings
  • Difficulty communicating
  • Limited attention span
  • Disorientation
  • Forgetfulness
  • Inappropriate behavior

Treatment and Recovery

Each brain injury patient’s treatment journey is different and depending on the goals of the patient, an individualized care plan is key for treatment and recovery. However, here’s a few examples of the kinds of standard treatments that a healthcare provider will recommend for your treatment:

Physical Therapy Exercises

Brain injury patients often come to us experiencing a range of motor issues, from reduced mobility and loss of balance to a total inability to walk or move around without assistance. We will work with you to create a personalized physical therapy plan to help you or your loved one regain mobility.

Occupational Therapy Exercises

The trauma that brain injury patients experience can greatly affect how they live their daily lives. Many people initially think about their job when they think of an occupation, but it also includes normal day-to-day activities. Occupational therapy helps patients re-learn what we call “activities of daily living,” which can include anything that occupies your time and is important for your well-being.

Occupational exercises can range from self-care activities like showering and getting dressed to more complex activities such as those required to work at a job. We will work with you to create an occupational therapy treatment plan that helps you or your loved one get back to life prior to injury.

Meningiomas are tumours that start in the layers of tissue (meninges) that cover the brain and spinal cord. Most meningiomas are not cancerous (benign).

The meninges are membranes that support and protect the brain and spinal cord. A clear fluid called cerebrospinal fluid (CSF) travels in the spaces formed by the meninges.

Meningiomas can start anywhere in the brain and spinal cord. Symptoms of meningioma depend on where the tumour is in the brain. Some meningiomas do not cause any symptoms. They might be picked up when you have a brain scan for something else.

If you have symptoms these might include:

  • fits (seizures)
  • weakness in your arms or legs
  • loss of eyesight
  • hearing loss

Types and grades of meningiomas

Doctors group meningiomas into groups depending on how quickly they are likely to grow. This is called the grade. They can be low grade (slow growing) or high grade (fast growing).

The grade depends on how the cells look. Generally, the more normal the cells look, the lower the grade. The more abnormal the cells look, the higher the grade. Grade also depends on genes and proteins in the tumour cells.

There are 3 grades of meningiomas: grade 1, grade 2 and grade 3.

Doctors also split meningiomas into subtypes. There are 15 different types of meningioma.

How common it is

Around 27 out of every 100 brain tumours (around 27%) diagnosed in England between 1995 and 2017 were meningiomas. It is the most common type of benign brain tumour diagnosed in the UK.

Meningiomas are more common in women than in men.

What tests will I have?

You have tests to diagnose a meningioma. Your doctor checks the size of the tumour and its location. This helps your doctor plan your treatment. The tests you might have include:

  • MRI scan or CT scan
  • a biopsy
  • blood tests
  • a test of your neurological system (neurological examination)
  • a scan to look at the blood vessels in your brain (brain angiogram)

Treating Meningiomas

Your treatment depends on whether the meningioma is low grade (slow growing) or high grade (fast growing). It also depends on where the tumour is.

MONITORING

For a low grade meningioma, your doctor might monitor you with regular MRI scans. This is called active monitoring. You then have treatment if there are signs that the tumour is growing.

SURGERY

A neurosurgeon removes as much of the tumour as possible. Sometimes this is the only treatment you need. The exact type of surgery you have depends on where the tumour is.

It isn’t always possible to completely remove the tumour during the operation. Especially if the tumour is growing around important nerves or blood vessels. You might have more surgery if doctors couldn’t remove all of the tumour. Or your doctor might suggest that you have radiotherapy.

RADIOTHERAPY

Radiotherapy uses high energy x-rays to kill tumour cells. You might have radiotherapy:

  • to reduce the risk of the meningioma coming back, especially if the tumour is fast growing
  • if the tumour is in an area that is too difficult to operate (for example, the base of the skull)
  • if you can’t have surgery for any reason
  • if the meningioma comes back

You may have a type of radiotherapy called stereotactic radiotherapy. It targets high doses of radiotherapy to the tumour. Doctors sometimes call this stereotactic radiosurgery, although it isn’t a type of surgery.

Follow up

You have regular appointments with your doctor or nurse after treatment finishes. Your doctor examines you at each appointment. They ask how you are feeling, whether you have had any symptoms or side effects, and if you are worried about anything. You also have MRI scans on some visits.

How often you have check ups depends on your individual situation.

For a grade 1 meningioma, you might have an MRI scan every year, for up to 5 years. You then have an MRI scan every 2 years.

For a grade 2 meningioma, you might have an MRI scan every 6 to 12 months. After 5 years, you have an MRI scan every 2 years.

For a grade 3 meningioma, you might have an MRI scan every 3 to 6 months. After 2 years, you have an MRI scan every 6 to 12 months.

Brain metastases happen when cancer cells spread from their original site to the brain. Any cancer can spread to the brain. But the most common types that spread are lung, breast, colon, kidney and melanoma.

Brain metastases may form one or more tumors in the brain. As they grow, they put pressure on surrounding brain tissue. This can cause symptoms such as headache, personality changes, confusion, seizures, vision changes, trouble speaking, numbness, weakness or loss of balance.

Treatment for people whose cancer has spread to the brain may include surgery, radiation therapy, immunotherapy, targeted therapy or chemotherapy. Other treatments might be used to decrease pain and symptoms caused by the cancer.

What are the symptoms?

Symptoms caused by brain metastases can vary. They depend on location, size and how fast they’re growing. Symptoms of brain metastases include:

  • Headache, sometimes with vomiting or nausea.
  • Mental changes, such as increasing memory problems.
  • Seizures.
  • Weakness or numbness on one side of the body.
  • Vision changes.
  • Difficulty speaking or understanding language.
  • Loss of balance.

Causes

Brain metastases occur when cancer cells break away from their original location. The cells may travel through the bloodstream or lymphatic system and spread to the brain.

Cancer that spreads from its original location is known by the name of the primary cancer. For example, cancer that has spread from the breast to the brain is called metastatic breast cancer, not brain cancer.

Diagnosis

Tests and procedures for diagnosing brain metastases include:

  • Neurological exam. Your healthcare professional checks your cognition, speech, vision, hearing, balance, coordination, strength, sensation and reflexes.
  • Imaging tests. These tests make pictures of the body. Magnetic resonance imaging, also called MRI, is the main test used to help show the location and size of brain metastases. A dye may be injected through a vein in your arm during this test.
  • Other imaging tests may include computerized tomography, also called CT, and positron emission tomography, also called PET.
  • Biopsy. Your healthcare professional may recommend a procedure to remove a sample of tissue for testing in a lab. It can be done with a needle or during surgery to remove a brain tumor.

Treating Brain Metatases

Treatment for brain metastases can help ease symptoms, slow tumor growth and extend life. Even with successful treatment, they may return. That’s why your healthcare professional will follow you closely.

Treatments will depend on the type, size, number and location of tumors. Healthcare professionals also consider your symptoms, health and treatment goals.

MEDICINES TO CONTROL SYMPTOMS

Medicines can help control symptoms of brain metastases and make you more comfortable. Options might include:

Steroids. These high-dose medicines also are called corticosteroids. They may decrease swelling in the brain caused by brain metastases, helping to relieve symptoms.
Anti-seizure drugs. These medicines may help control seizures if you have any.

SURGERY

Surgery may be an option if a tumor is easily reachable and fits into your overall cancer care plan. The surgeon will remove as much tumor as possible. Surgery may help improve symptoms and help with diagnosis. It is combined with other treatments.

Brain surgery risks have improved significantly over the years. But risks may include problems with thinking, moving and speaking, as well as numbness or weakness in the face, arms or legs. Infection and bleeding are other possible risks. Risks may depend on where the tumors are in the brain.

RADIATION THERAPY

Radiation therapy treats cancer with powerful energy beams. The energy can come from X-rays, protons or other sources. During radiation therapy, you lie on a table while a machine moves around you. The machine directs radiation to precise points in your brain.

Treatment may include one or both of the following:

Whole-brain radiation. Whole-brain radiation aims beams at the entire brain to kill tumor cells. People having whole-brain radiation usually need 10 to 15 treatments over 2 to 3 weeks. Side effects may include fatigue, nausea, skin reaction, headache and hair loss. Long-term, whole-brain radiation may cause decline in thinking and memory.

Stereotactic radiosurgery. Stereotactic radiosurgery is a focused radiation treatment. It also is called SRS or stereotactic body radiotherapy. SRS aims beams of radiation from many angles at the cancer. Healthcare professionals use 3D planning to make the treatment as exact as possible and limit damage to healthy parts of the brain. Stereotactic radiosurgery may take one or a few treatments. Side effects may include nausea, headache, seizures and dizziness. The risk of thinking and memory decline after SRS is thought to be less than with whole-brain radiation.

Healthcare professionals have made major advances understanding whole-brain radiation and stereotactic radiosurgery. They have learned how these therapies affect survival, brain function and quality of life. In deciding which radiation therapy to have, you and your healthcare professional will consider many factors. These include the number of brain metastases present, other treatments you’re getting and how likely your cancer is to recur.

MEDICINES

Sometimes, your healthcare team may recommend medicines to control your brain metastases. Whether they may help depends on where your cancer started and your own situation. Options may include:

Chemotherapy. Chemotherapy treats cancer with strong medicines. Many chemotherapy medicines exist. Most chemotherapy medicines are given through a vein. Some come in pill form.
Targeted therapy. Targeted therapy for cancer is a treatment that uses medicines that attack specific chemicals in the cancer cells. By blocking these chemicals, targeted treatment can cause cancer cells to die.
Immunotherapy. Immunotherapy for cancer is a treatment with medicine that helps the body’s immune system kill cancer cells. The immune system fights off diseases by attacking germs and other cells that shouldn’t be in the body. Cancer cells survive by hiding from the immune system.

Rehabilitation after treatment

Brain tumors may form in parts of the brain that control movement, speech, vision and thinking. That’s why rehabilitation may need to be part of recovery. Your healthcare professional may refer you to these services:

Physical therapy. Physical therapists can help you regain strength, coordination, and the ability to move and balance.
Occupational therapy. Occupational therapists can help you return to your usual daily activities, such as work.
Speech therapy. Speech pathologists can work with you if you have trouble speaking.
Cognitive rehabilitation therapy. Healthcare professionals can help if you are having difficulty with memory loss, word recall, mood issues and attention.

A stroke is when blood stops flowing to a part of your brain. It can affect things like speech and movement, and take a long time to recover. A stroke needs urgent medical help in hospital because it can be life-threatening.

Symptoms of a Stroke

The main symptoms of a stroke can happen suddenly. They may include:

  • face weakness – one side of your face may droop (fall) and it might be hard to smile
  • arm weakness – you may not be able to fully lift both arms and keep them there because of weakness or numbness in 1 arm
  • speech problems – you may slur your words or sound confused

The easiest way to remember these symptoms is the word FAST. This stands for: face, arms, speech and time to call 999.There are other signs that you or someone else is having a stroke. These include:

  • weakness or numbness down 1 side of your body
  • blurred vision or loss of sight in 1 or both eyes
  • finding it difficult to speak or think of words
  • confusion and memory loss
  • feeling dizzy or falling over
  • a severe headache
  • feeling or being sick (nausea or vomiting)

Symptoms of a stroke can sometimes stop after a short time, so you may think you’re OK. Even if this happens, get medical help straight away.

A stroke is more likely to happen if you’re older, but it can happen at any age.

Causes of a Stroke

A stroke can happen to anyone at any age, but your risk may increase if:

  • you’re over 50 years old
  • you’re from a Black or South Asian background
  • you have sickle cell disease (SCD)
  • you have an unhealthy lifestyle
  • you have migraines
  • you take the combined contraceptive pill
  • you’re pregnant and have pre-eclampsia
  • you’ve just had a baby

Certain conditions also increase the risk of stroke. These include:

  • high blood pressure (hypertension)
  • diabetes
  • irregular and fast heartbeats (atrial fibrillation)
  • high cholesterol
  • a transient ischaemic attack (TIA or mini stroke)

If you have a stroke, or a transient ischaemic stroke (TIA, or mini-stroke), you’re more at risk of having another stroke. But there are things you can do to lower the risk such as quitting smoking, eating a balanced diet, exercising and cutting down on alcohol. It is also important that you do not forget to take medicines for any underlying conditions such as high blood pressure or diabetes.

Diagnosing a stroke

If a doctor thinks you’ve had a stroke, they’ll do tests such as:

  • blood tests
  • CT, MRI and ultrasound scans to check in and around your brain
  • an electrocardiogram (ECG) to check your heart

These tests can show what type of stroke you’ve had. The different types of stroke include:

  • an ischaemic stroke – this happens when a blood clot blocks blood flow to the brain. It’s the most common type of stroke
  • a haemorrhagic stroke – this happens when a blood vessel bursts
  • a transient ischaemic attack (TIA or mini stroke) – this is when the symptoms of a stroke do not last very long (less than 24 hours)

A TIA should be treated as urgent. If you do not get immediate medical attention, you could be at risk of having a full stroke.

Treatment for a stroke

If you have a stroke, your treatment will depend on what type of stroke you’ve had. In the first 24 hours after a stroke, your treatment may include:

  • medicine to get rid of blood clots in the brain (thrombolysis)
  • surgery to remove a blood clot (thrombectomy) or drain fluid from the brain
  • a procedure to stop pressure building up inside the skull or brain

While you’re in hospital, a healthcare team of doctors, specialists and therapists will help you start your recovery.

MEDICINES FOR A STROKE

Treatments you may be given, often long term, include:

  • anticoagulants to stop blood clots forming
  • medicines to lower your blood pressure
  • statins to lower your cholesterol

If the GP cannot identify a more likely cause of your symptoms, they may refer you to a neurologist like Dr Davies who specialises in the brain and nervous system for further assessment and tests, such as a brain scan.

Syncope is also called fainting or passing out.

It most often occurs when blood pressure is too low and the heart doesn’t pump enough oxygen to the brain. It can be harmless or a symptom of an underlying medical condition.

What causes syncope?

Syncope is a symptom that can have several causes, ranging from harmless to life-threatening conditions. Many non-life-threatening factors, such as strong emotions, heavy sweating, exhaustion or the pooling of blood in the legs due to sudden changes in body position, can trigger syncope. It’s important to determine the cause of syncope and any underlying conditions.

However, several serious heart conditions, such as bradycardia, tachycardia or blood flow obstruction, can also cause syncope.

What is neurally mediated syncope?

Neurally mediated syncope (NMS) is the most common form of fainting and a frequent reason for emergency department visits. It’s also called reflex, neurocardiogenic, vasovagal (VVS) or vasodepressor syncope. It’s harmless and rarely requires medical treatment.

NMS is more common in children and young adults, though it can occur at any age. It happens when the part of the nervous system that regulates blood pressure and heart rate malfunctions in response to a trigger, such as emotional stress or pain.

NMS usually happens after standing for a long time. It is often preceded by a sensation of warmth, nausea, lightheadedness, tunnel vision or visual “gray out.” Placing the person in a reclining position restores blood flow and consciousness.

Situational syncope, which is a type of NMS, is related to certain physical functions, such as violent coughing (especially in men), laughing, swallowing or urination.

Other disorders can cause syncope. It can also be caused by some medications.

Some types of syncope that suggest a serious disorder are those:

  • Occurring during exercise or exertion
  • Associated with palpitations or irregularities of the heart
  • Associated with family history of recurrent syncope, heart disease at a young age or sudden death

What are the risk factors?

Syncope is common, and older adults are at greater risk of hospitalization and death.

Younger people without heart disease but who’ve had syncope while standing or have specific stress or situational triggers aren’t as likely to have cardiac syncope. Cardiac syncope is a higher risk in men and those over age 60. People with the following are also at higher risk:

  • Known ischemic heart disease, structural heart disease, previous arrhythmias or reduced ventricular function
  • Brief palpitations or sudden loss of consciousness
  • Fainting during exertion
  • Fainting while flat on one’s back
  • Low number of fainting episodes (one or two)
  • Abnormal heart exam
  • Family history of inheritable conditions or premature sudden cardiac death (younger than age 50)
  • Presence of known congenital heart disease

A traumatic brain injury (TBI) refers to a brain injury that is caused by an outside force. TBI can be caused by a forceful bump, blow, or jolt to the head or body, or from an object entering the brain. Not all blows or jolts to the head result in TBI.

Some types of TBI can cause temporary or short-term problems with brain function, including problems with how a person thinks, understands, moves, communicates, and acts. More serious TBI can lead to severe and permanent disability, and even death.

Some injuries are considered primary, meaning the damage is immediate. Others can be secondary, meaning they can occur gradually over the course of hours, days, or weeks after injury. These secondary brain injuries are the result of reactive processes that occur after the initial head trauma.

There are two broad types of head injuries: Penetrating and non-penetrating.

  • Penetrating TBI (also known as open TBI) happens when an object pierces the skull (e.g., a bullet, shrapnel, bone fragment, etc.) and enters the brain tissue. Penetrating TBI typically damages only part of the brain.
  • Non-penetrating TBI (also known as closed head injury or blunt TBI) is caused by an external force strong enough to move the brain within the skull. Causes include falls, motor vehicle crashes, sports injuries, blast injury, or being struck by an object.

Some accidents or trauma can cause both penetrating and non-penetrating TBI in the same person.

Symptoms of traumatic brain injury

Headache, dizziness, confusion, and fatigue tend to start immediately after an injury but resolve over time. Emotional symptoms such as frustration and irritability tend to develop during recovery. Seek immediate medical attention if the person experiences any of the following symptoms, especially within the first 24 hours after an injury to the head:

Physical symptoms of TBI

  • Headache
  • Convulsions or seizures
  • Blurred or double vision
  • Unequal eye pupil size or dilation
  • Clear fluids draining from the nose or ears
  • Nausea and vomiting
  • New neurological problems, such as slurred speech, weakness of arms, legs, or face, or loss of balance

Cognitive/behavioral symptoms of TBI

  • Loss of or change in consciousness for anywhere from a few seconds to a few hours
  • Decreased level of consciousness (e.g., hard to awaken)
  • Confusion or disorientation
  • Problems remembering, concentrating, or making decision
  • Changes in sleep patterns (e.g., sleeping more, difficulty falling or staying asleep, inability to wake)
  • Frustration, irritability

Perception and sensation symptoms of TBI

  • Light-headedness, dizziness, vertigo, or loss of balance or coordination
  • Blurred vision
  • Hearing problems, such as ringing in the ears
  • Unexplained bad taste in the mouth
  • Sensitivity to light or sound
  • Mood changes or swings, agitation, combativeness, or other unusual behavior
  • Feeling anxious or depressed
  • Fatigue or drowsiness; a lack of energy or motivation

TBI’s effects on consciousness

A TBI can cause problems with consciousness, awareness, alertness, and responsiveness. Generally, there are four abnormal states that can result from a severe TBI:

  • Minimally conscious state. People in this state still display some evidence of self-awareness or awareness of their environment (such as following simple commands and giving yes or no responses).
  • Unresponsive wakefulness syndrome (UWS). A result of widespread damage to the brain, people with UWS are unconscious and unaware of their surroundings. However, they can have periods of unresponsive alertness and may groan, move, or show reflex responses.
  • Coma. A person in a coma is unconscious, unaware, and unable to respond to external stimuli such as pain or light. Coma generally lasts a few days or weeks, after which the person may regain consciousness, die, or move into a vegetative state.
  • Brain death. The lack of measurable brain function and activity after an extended period of time is called brain death and can be confirmed by tests that show blood is not flowing to the brain.

How does TBI affect the brain?

TBI-related damage can be confined to one area of the brain, known as a focal injury, or it can occur over a more widespread area, known as a diffuse injury. The type of injury also affects how the brain is damaged. The types of damage usually seen in the brain from a TBI include bleeding, swelling, and tearing that injures nerve fibers. This damage can cause inflammation, swelling, and metabolic changes.

Diffuse axonal injury (DAI), one of the most common types of brain injuries, refers to widespread damage to the brain’s white matter. DAI commonly occurs in auto accidents, falls, or sports injuries. It can disrupt and break down communication among nerve cells in the brain. It also leads to the release of brain chemicals that can cause further damage. Brain damage may be temporary or permanent and recovery can take a long time.

Concussion is a type of mild TBI that may be considered a temporary injury to the brain but could take minutes to several months to heal. Concussion may be caused by a blow to the head, a sports injury or fall, a motor vehicle accident, or a rapid movement of the brain within the skull, as can happen when a person is violently shaken. The individual with concussion either suddenly loses consciousness or their state of conscious or awareness changes suddenly. A second concussion closely following the first one—the so-called “second hit” phenomenon—and can lead to permanent damage or even death in some instances. Post-concussion syndrome involves symptoms that last for weeks or longer.

Hematomas are bleeding in and around the brain caused by a burst blood vessel. Different types of hematomas form depending on where the blood collects in the protective membranes surrounding the brain, which include the dura mater (outermost), arachnoid mater (middle), and pia mater (innermost).

  • Epidural hematomas involve bleeding into the area between the skull and the dura mater. These can occur within minutes to hours after injury and are particularly dangerous.
  • Subdural hematomas involve bleeding between the dura and the arachnoid mater, and, like epidural hematomas, exert pressure on the outside of the brain. They are very common in older adults after a fall.
  • Subarachnoid hemorrhage is bleeding between the arachnoid mater and the pia mater.
  • Intracerebral hematoma involves bleeding into the brain itself and damages the surrounding tissue.

Contusions are a bruising or swelling of the brain that occurs when very small blood vessels bleed into brain tissue. Contusions can occur directly under the impact site (a coup injury) or, more often, on the complete opposite side of the brain from the impact (a contrecoup injury). They can appear after a delay of hours to a day. These generally occur when the head abruptly decelerates, which causes the brain to bounce back and forth within the skull (such as in a high-speed car crash or in shaken baby syndrome).

Skull fractures are breaks or cracks in one or more of the bones that form the skull. They are a result of blunt force trauma and can cause damage to the membranes, blood vessels, and brain under the fracture. Helmets can help prevent skull fractures.

Chronic traumatic encephalopathy (CTE) is a progressive neurological disorder with symptoms that may include problems with thinking, understanding, and communicating; movement disorders; problems with impulse control and depression; confusion; and irritability. While it was originally identified only at autopsy, research to date suggests CTE may be caused in part by repeated TBIs. It develops over years and can take years to show symptoms. Studies of retired boxers have shown that repeated blows to the head can cause issues including memory problems, tremors, lack of coordination, and dementia. Recent studies have demonstrated cases of CTE in other sports with repetitive mild head impacts (e.g., soccer, wrestling, football, and rugby). NINDS supports ongoing research to refine the diagnostic criteria for CTE.

Post-traumatic dementia (PTD) can arise after a single, severe TBI. PTD may be progressive and share some features with CTE. Studies assessing patterns among large populations of people with TBI indicate that moderate or severe TBI in early or mid-life may be associated with increased risk of dementia later in life.

The initial damage to the brain described above can itself cause secondary damage. Secondary damage refers to the changes occur over a period of hours to days after the primary brain injury. Examples of secondary damage include:

Hemorrhagic progression of a contusion (HPC) are injuries that occur when a contusion continues to bleed in and around the brain and expand over time. This creates a new or larger lesion and leads to swelling and further brain cell loss.

A breakdown in the blood-brain barrier refers to the disruption of the network that controls the movement of cells and molecules between the blood and fluid that surrounds the brain’s nerve cells. Once the blood-brain barrier is disrupted, blood, plasma proteins, and other foreign substances leak into the space between neurons in the brain and trigger a chain reaction that causes brain swelling. It also causes inflammatory responses which can be harmful to the body if they continue for an extended period of time and the inappropriate release of neurotransmitters, which can damage or kill nerve cells.

Increased intracranial pressure is usually caused by brain swelling inside the skull as a result of the injury. This pressure can damage brain tissue and prevent blood flow to the brain, depriving it of the oxygen it needs to function.

Other secondary damage can be caused by infections to the brain, low blood pressure or oxygen flow as a result of the injury, hydrocephalus, and seizures.

Diagnosing TBI

All TBIs should be evaluated immediately a professional who has experience with head injuries. A neurological exam will judge motor and sensory skills and test hearing and speech, coordination and balance, mental status, and changes in mood or behavior, among other abilities.

Screening tools developed for coaches and athletic trainers can identify the most concerning concussions for medical evaluation.

Medical providers can use brain imaging to evaluate the extent of the primary brain injuries and determine if surgery will be needed to help repair any damage to the brain. A physical examination by a doctor and the person’s symptoms will help determine whether imaging is needed. Commonly used imaging for TBI includes CT (computed tomography) and MRI (magnetic resonance imaging). CT imaging can show a skull fracture and any brain bruising, bleeding, or swelling. MRI is more sensitive and can pick up more subtle brain changes that a CT scan may miss.

Significant advances have been made in the last decade to detect milder TBI damage via imaging. For example, diffusion tensor imaging can identify white matter tracts, fluid-attenuated inversion recovery can detect small areas of damage, and susceptibility-weighted imaging can identify even small and hard to detect brain bleeds. Despite these improvements, currently available imaging technologies, blood tests, and other measures cannot always diagnose mild concussive injuries.

Neuropsychological tests to gauge brain functioning are often used along with imaging in people who have suffered mild TBI. Such tests involve performing specific tasks that help assess memory, concentration, information processing, executive functioning, reaction time, and problem solving.

Many athletic organizations recommend establishing a baseline picture of an athlete’s brain function at the beginning of each season, ideally before any head injuries occur. Brain function tests yield information about an individual’s memory, attention, and ability to concentrate and solve problems. Brain function tests can be repeated at regular intervals (every one to two years) and also after a suspected concussion. The results may help healthcare providers identify any effects from an injury and allow them to make more informed decisions about whether a person is ready to return to their normal activities.

Treating TBI

Many factors—including the size, severity, and location of the brain injury—influence how TBI is treated and how quickly a person might recover. Although brain injury often occurs at the moment of head impact, much of the damage related to severe TBI develops from secondary injuries which happen days or weeks after the initial trauma. For this reason, people who receive immediate medical attention at a certified trauma center tend to have the best health outcomes.

Genetics may play a role in how quickly and completely a person recovers from a TBI. For example, researchers have found that apolipoprotein E ε4 (ApoE4) — a genetic variant associated with higher risks for Alzheimer’s disease — is associated with worse health outcomes following a TBI. Much work remains to be done to understand how genetic factors, as well as specific types of head injuries, affect recovery.

Studies suggest that age and the number of head injuries a person has suffered over his or her lifetime are two critical factors that impact recovery. Brain swelling in newborns, young infants, and teenagers often occurs much more quickly than it does in older people. Evidence from very limited CTE studies suggest that younger people (ages 20 to 40) tend to have more behavioral and mood changes with CTE, while those who are older (ages 50+) tend to have more cognitive difficulties.

Compared with younger adults with the same TBI severity, older adults are more likely to have lasting symptoms. Older people often have other medical issues and may be taking multiple medications, which may complicate treatment. For example, blood thinning medications may increase the risk of bleeding in the brain.

MILD TBI

Some people with mild TBI (such as a concussion) may not require treatment other than rest and over-the-counter pain relievers. Treatment should focus on symptom relief and “brain rest.” Brain rest means avoiding activities that require concentration or attention. The person should be monitored by their healthcare provider to note new or worsening symptoms.

Children and teens who have a sports-related concussion should stop playing immediately and return to play only after being approved by a concussion specialist.

Preventing future concussions is critical. While most people recover fully from a first concussion within a few weeks, the rate of recovery from a second or third concussion is generally slower.

Even after concussion symptoms go away, people should return to their daily activities gradually, and only once they have permission from a doctor. While there are some guidelines available, further research is needed to better understand the effects of mild TBI on the brain and determine when it is safe to resume normal activities.

People with mild TBI should:

  • Make an appointment for a follow-up visit with their healthcare provider to confirm the progress of their recovery
  • Inquire about new or ongoing symptoms and how to treat them
  • Pay attention to any new signs or symptoms even if they seem unrelated to the injury (for example, mood swings, unusual feelings of irritability). These symptoms may be related even if they occurred several weeks after the injury.

Medications to treat symptoms of TBI may include:

  • Over-the-counter or prescribed pain medicines
  • Anticonvulsant drugs to treat seizures
  • Anticoagulants to prevent blood clots
  • Diuretics to help reduce fluid buildup and reduce pressure in the brain
  • Stimulants to increase alertness
  • Antidepressants and anti-anxiety medications to treat depression and feelings of fear and nervousness

SEVERE TBI

Immediate treatment for someone who has a severe TBI focuses on preventing death; stabilizing the person’s spinal cord, heart, lung, and other vital organ functions; ensuring proper oxygen delivery and breathing; controlling blood pressure; and preventing further brain damage. Emergency care staff will monitor the flow of blood to the brain, brain temperature, pressure inside the skull, and the brain’s oxygen supply.

A person with severe TBI may need surgery to relieve pressure inside the skull, remove debris, dead brain tissue, or hematomas, or repair skull fractures. While in the hospital for severe TBI, the person should be monitored for infection (particularly pneumonia) and deep vein thrombosis (blood clots that can form during long periods of inactivity).

For more information please don’t hesitate to contact us at info@djdsurgery.co.uk and a member of our team will get back to you as soon as possible.

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