A pleural effusion is an unusualamount of fluid around the lung.There are many medicalconditions that can lead to it. Soeventhough your pleural effusionmay have to be drained, yourdoctor likely will target thetreatment at whatever caused it.
The pleura is a thin membranethat lines the surface of the lungsand the inside of the chest walloutside the lungs. In pleuraleffusions, fluid builds up in thespace between the layers of pleura.
Normally, only teaspoons of watery fluid are in the pleural space, allowingthe lungs to move smoothly within the chest cavity during breathing.
A wide range of things can cause a pleural effusion. Some of the morecommon ones are:
You might not have any. You’re more likely to have symptoms when a pleuraleffusion is moderate or large-sized, or if inflammation is present.
If you do have symptoms, they may include:
Doctors use the terms “transudative” and “exudative” to describe the two main types of pleural effusions:
Transudative: This pleural effusion fluid is similar to the fluid you normally have in your pleural space. It forms from liquid leaking across normal pleura. This type of pleural effusion rarely needs to be drained unless they are very large. Congestive heart failure is the most common cause of this type of effusion.
Exudative: This effusion forms from excess liquid, protein, blood, inflammatory cells or sometimes bacteria leaking across damaged blood vessels into the pleura. It may need to be drained, depending on its size and how much inflammation is involved. Among its causes are pneumonia and lung cancer.
Your doctor may need to treat only the medical condition that caused the pleural effusion. You would get antibiotics for pneumonia, for instance, or diuretics for congestive heart failure.
Large, infected, or inflamed pleural effusions often need to be drained to help you feel better and to prevent more problems. Procedures for treating pleural effusions include:
A cold or the flu runs its course in a couple weeks, if you’re lucky. After that, you’re back to normal. But sometimes you may get bronchitis, too.
That’s when your bronchial tubes, which carry air to your lungs, get infected and swollen. You end up with a nagging cough and a lot more mucus.
You can get bronchitis in other ways, too, and there are actually two types of it:
Most often, the same viruses that give you a cold or the flu also cause bronchitis. Sometimes, though, bacteria are to blame.
In both cases, as your body fights off the germs, your bronchial tubes swell and make more mucus. That means you have smaller openings for air to flow, which can make it harder to breathe.
If any of these things describe your situation, you have a bigger chance of getting bronchitis:
You’ll definitely have a cough, and you may have various problems with breathing, such as:
You may also:
Even after the other symptoms are gone, the cough can last for a few weeks while your bronchial tubes heal and the swelling goes down. If it goes on much longer than that, the problem might be something else.
Most of the time, bronchitis goes away on its own within a couple of weeks.
If yours is caused by bacteria (which is rare), your doctor may give you antibiotics.
If you have asthma, allergies, or you’re wheezing, she might suggest an inhaler. This helps open up your airways and makes it easier to breathe.
To ease your symptoms, you can:
Here are some ways to lower your chances of getting bronchitis:
The large intestine is the lowest section of your digestive tract. It includes your appendix, colon, and rectum. The large intestine completes the digestive process by absorbing water and passing waste (stool) to the anus.
Certain conditions can cause the large intestine to malfunction. One such condition is toxic megacolonor megarectum. Megacolon is a general term that means the abnormal dilation of the colon. Toxic megacolon is a term used to express the seriousness of the condition.
Toxic megacolon is rare. It’s a widening of the large intestine that develops within a few days and can be life-threatening. It can be a complication of inflammatory bowel disease (such as Crohn’s disease).
What causes toxic megacolon?
One of the causes of toxic megacolon is an inflammatory bowel disease (IBD). Inflammatory bowel diseases cause swelling and irritation in parts of your digestive tract. These diseases can be painful and cause permanent damage to your large and small intestines. Examples of IBDs are ulcerative colitis and Crohn’s disease. Toxic megacolon can also be caused by infections such as Clostridium difficile colitis.
Toxic megacolon occurs when inflammatory bowel diseases cause the colon to expand, dilate, and distend. When this happens, the colon is unable to remove gas or feces from the body. If gas and feces build up in the colon, your large intestine may eventually rupture.
Rupture of your colon is life-threatening. If your intestines rupture, bacteria that are normally present in your intestine release into your abdomen. This can cause a serious infection and even death.
It’s important to note that there are other types of megacolon. Examples include:
Although these conditions can expand and damage the colon, they’re not due to inflammation or infection.
When toxic megacolon occurs, the large intestines rapidly expand. Symptoms of the condition may come on suddenly and include:
Toxic megacolon is a life-threatening condition. If these symptoms develop, you should seek immediate medical attention.
The treatment of toxic megacolon usually involves surgery. If you develop this condition, you will be admitted to the hospital. You will receive fluids to prevent shock. Shock is a life-threatening condition that occurs when an infection in the body causes your blood pressure to decrease rapidly.
Once your blood pressure is stable, you’ll need surgery to correct toxic megacolon. In some cases, toxic megacolon may produce a tear or perforation in the colon. This tear must be repaired to prevent bacteria from the colon from entering the body.
Even if there’s no perforation, the tissue of the colon may be weakened or damaged and need removal. Depending on the extent of the damage, you may need to undergo a colectomy. This procedure involves either a complete or partial removal of the colon.
You’ll take antibiotics during and after the surgery. Antibiotics will help prevent a serious infection known as sepsis. Sepsis causes a severe reaction in the body that is often life-threatening.
If you develop toxic megacolon and promptly seek treatment at a hospital, your long-term outlook will be good. Seeking emergency medical treatment for this condition will help prevent complications, including:
If complications of toxic megacolon occur, your doctor may have to take serious measures. Complete removal of the colon may require you to have an ileostomy or ileoanal pouch-anal anastomosis (IPAA) put in place. These devices will remove feces from your body after your colon is removed.
Henoch-Schonlein purpura (HSP) is a disease involving inflammation of small bloodvessels. It most commonly occurs in children. The inflammationcauses blood vessels in the skin, intestines, kidneys, and joints to start leaking. The main symptom is a rash with numerous small bruises, which have a raised appearance, over the legs or buttocks.
Although HSP can affect people at any age, most cases occur in children between the ages of 2 and 11. It is more common in boys than girls. Adults with HSP are more likely to have more severe disease compared to children.
HSP usually ends after four to six weeks — sometimes with recurrence of symptoms over this period, but with no long-term consequences. If organs such as the kidneys and intestines are affected, treatment is often needed and it is important to have regular follow-up to prevent serious complications.
The exact cause of HSP is not known. The body’s immune system is believed to play a role in targeting the blood vessels involved. An abnormal immune response to an infection may be a factor in many cases. Approximately two-thirds of the cases of HSP occur days after symptoms of an upper respiratory tract infection develop.
Some cases of HSP have been linked to vaccinations for typhoid, cholera, yellow fever, measles, or hepatitis B; foods, drugs, chemicals, and insect bites. Some experts also say that HSP is associated with the colder weather of fall and winter.
The classic symptoms of HSP are rash, joint pain and swelling, abdominal pain, and/or related kidney disease, including blood in urine. Before these symptoms begin, patients may have two to three weeks of fever, headache, and muscular aches and pains. Rarely, other organs, such as the brain, heart, or lungs, may be affected.
Here are some key details about the symptoms of HSP:
Rash. The rash usually appears in all patients with HSP. The initial appearance may resemble hives, with small red spots or bumps on the lower legs, buttocks, knees, and elbows. But these change to appear more like bruises. The rash usually affects both sides of the body equally and does not turn pale on pressing.
Arthritis. Joint inflammation, involving pain and swelling, occurs in approximately three-quarters of cases, particularly affecting the knees and ankles. It usually lasts only a few days and does not cause any long-term, chronic joint problems.
Abdominal pain. In more than half of people with HSP, inflammation of the gastrointestinal tract may cause pain or cramping; it may also lead to loss of appetite, vomiting, diarrhea, and occasionally blood in the stool.
In some cases, patients may have abdominal pain before the rash appears. In rare cases, an abnormal folding of the bowel (intussusception) may cause a bowel blockage, which may require surgery to fix.
Kidney impairment. HSP can cause kidney problems, indicated by such signs as protein or blood in the urine. This is usually only discovered on urine testing, since it does not generally cause any discomfort.
In most patients, the kidney impairment is mild and goes away without any long-term damage. It’s important to monitor the kidney problems closely and make sure they clear up, since about 5% of patients may develop progressive kidney disease. About 1% may go on to develop total kidney failure.
The diagnosis of HSP may be clear when the typical rash, arthritis, and abdominal pain are present. A doctor may order some tests to rule out other diagnoses, confirm the diagnosis, and assess its severity.
Occasionally, when the diagnosis is uncertain, particularly if the only symptom is the classic rash, your doctor may perform biopsies of the skin or kidney. Urine and blood tests will likely be done to detect signs of kidney involvement and may need to be repeated during follow-up to monitor any changes in kidney function.
Although there is no specific treatment for HSP, you can use over-the-counter pain medicines, such as acetaminophen or nonsteroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen and naproxen for joint pain. In some cases, corticosteroid medication may be used.
The rash and joint pain will usually go away after four to six weeks without causing any permanent damage. Bouts of the rash may recur in approximately one-third of cases, but they are usually milder, do not involve joint and abdominal symptoms, and they clear up on their own.
Fecal incontinence is the inability to control bowel movements. It’s a common problem, especially among older adults.
Accidental bowel leakage is usually not a serious medical problem. But it can seriously interfere with daily life. People with bowel incontinence may avoid social activities for fear of embarrassment.
Many effective treatments can help people with bowel incontinence. These include:
Talking to your doctor is the first step toward freedom from bowel incontinence.
The most common cause of bowel incontinence is damage to the muscles around the anus (anal sphincters). Vaginal childbirth can damage the anal sphincters or their nerves. That’s why women are affected by accidental bowel leakage about twice as often as men.
Anal surgery can also damage the anal sphincters or nerves, leading to bowel incontinence.
There are many other potential causes of bowel incontinence, including:
More than one cause for bowel incontinence is frequently present. It’s also not unusual for bowel incontinence to occur without a clear cause.
Discussing bowel incontinence may be embarrassing, but it can provide clues for a doctor to help make the diagnosis. During a physical examination, a doctor may check the strength of the anal sphincter muscle using a gloved finger inserted into the rectum.
Stool testing. If diarrhea is present, stool testing may identify an infection or other cause.
Endoscopy. A tube with a camera on its tip is inserted into the anus. This identifies any potential problems in the anal canal or colon. A short, rigid tube (anoscopy) or a longer, flexible tube (sigmoidoscopy or colonoscopy) may be used.
Surgery may be recommended for people whose bowel incontinence is not helped by noninvasive treatments. The types of surgery include:
Anorectal manometry. Apressure monitor is inserted intothe anus and rectum. This allowsmeasurement of the strength ofthe sphincter muscles.
Endosonography. An ultrasoundprobe is inserted into the anus.This produces images that canhelp identify problems in the anal and rectal walls.
Nerve tests. These tests measure the responsiveness of the nervescontrolling the sphincter muscles. They can detect nerve damage thatcan cause bowel incontinence.
MRI defecography. Magnetic resonance imaging of the pelvis can beperformed, potentially while a person moves her bowels on a specialcommode. This can provide information about the muscles and supportingstructures in the anus, rectum, and pelvis.
Bowel incontinence is usually treatable. In many cases, it can be cured completely.
Recommended treatments vary acc
Medications. Try these medicines to reduce the number of bowel movements and the urge to move the bowels:
Methylcellulose can help make liquid stool more solid and easier to control. For people with a specific cause of diarrhea, such as inflammatory bowel syndrome, other medications may also help.
Exercises. Begin a program of regularly contracting the muscles used to control urinary flow (Kegel exercises). This builds strength in the pelvic muscles and may help reduce bowel incontinence.
Bowel training. Schedule bowel movements at the same times each day. This can help prevent accidents in between.
Biofeedback. A sensor is placed inside the anus and on the abdominal wall. This provides feedback as a person does exercises to improve bowel control.
Many people with dilated cardiomyopathy have no symptoms. Some that do have only minor ones, and live a normal life. Others develop symptoms that may get worse as their heart gets sicker.
Symptoms of DCM can happen at any age and may include:
DCM can be inherited, but it’s usually caused by other things, including:
It can also happen in women after they give birth. That’s called postpartum cardiomyopathy.
Your doctor will decide if you have DCM after he looks at things like:
Another test that’s rarely done to find the cause of cardiomyopathy is called a myocardial biopsy, or heart biopsy. A tissue sample is taken from the heart and examined under a microscope.
If you have a relative with dilated cardiomyopathy, ask your doctor if you should be screened for it. Genetic testing may also be available to find abnormal genes.
In the case of dilated cardiomyopathy, it’s aimed at making the heart stronger and getting rid of substances in the bloodstream that enlarge the heart and lead to more severe symptoms:
Medications: To manage heart failure, most people take drugs, such as a:
If you have an arrhythmia(irregular heartbeat), your doctor may give you medicine to control your heart rate or make them happen less often. Blood thinners may also be used to prevent blood clots.
Lifestyle changes: If you have heart failure, you should have less sodium, based on your doctor’s recommendations. He may point you toward aerobic exercise, but don’t do heavy weightlifting.
People with severe DCM may need one of the following surgeries:
Cardiac resynchronization by biventricular pacemaker: For some people with DCM, stimulating the right and left ventricles with this helps your heart’s contractions get stronger. This improves your symptoms and lets you exercise more.
The pacemaker also will help people with heart block (a problem with the heart’s electrical system) or some bradycardias (slow heart rates).
Implantable cardioverter defibrillators (ICD): These are suggested for people at risk for life-threatening arrhythmias or sudden cardiac death. It constantly monitors your heart’s rhythm. When it finds a very fast, abnormal rhythm, it ”shocks” the heart muscle back into a healthy beat.
Surgery: Your doctor may recommend a surgery for coronary artery disease or valve disease. You may be eligible for one to fix your left ventricle or one that gives you a device to help your heart work better.
Heart transplant: These are usually just for those with end-stage heart failure. You’ll go through a selection process. Hearts that can be used are in short supply. Also, you must be both sick enough that you need a new heart, and healthy enough to have the procedure.
Wernicke-Korsakoff syndrome (WKS) is a type of brain disorder caused by a lack of vitamin B-1. The syndrome is actually two separate conditions that can occur at the same time. Usually, people get the symptoms of Wernicke’s encephalopathy first.
Also called Wernicke’s disease, people with Wernicke’s encephalopathy have bleeding in the lower sections of the brain, including the thalamus and hypothalamus. These areas of the brain control the nervous and endocrine systems. The bleeding causes brain damage that presents symptoms involving your vision, coordination, and balance.
The signs of Korsakoff psychosis tend to follow as the Wernicke’s symptoms decrease. If Wernicke’s disease is treated quickly and effectively, Korsakoff syndrome may not develop. Korsakoff psychosis is the result of chronic brain damage. Korsakoff syndrome affects the areas of your brain that control memory.
Alcoholism, or chronic alcohol abuse, is the most common cause of WKS. WKS can also be linked to diet deficiencies or other medical conditions that impair vitamin B-1 absorption. Vitamin B-1 is also called thiamine.
To diagnose WKS, your doctor will look for clinical signs that point to a vitamin B-1 deficiency. This can include blood tests that measure thiamine levels and your general nutritional health, as well as tests to check your liver function.
Chronic alcoholism can damage your liver, elevating your liver enzymes. Diagnosis includes a physical examination to assess your:
After diagnosis, your doctor will most likely give you vitamin B-1 intravenously, or through your vein. Fast treatment may reverse many of the neurological symptoms of WKS.
The key to recovery is maintaining adequate vitamin B-1 levels, which means refraining from alcohol abuse if you have WKS. You should also eat a balanced diet.
Risk factors for WKS are related to your diet and lifestyle.
The major risk factors for developing WKS are malnourishment and chronic alcoholism. Other risk factors for WKS include:
Causes of WKS:
The number one cause of WKS is alcoholism.
The less common causes of WKS are conditions that limit nutritional absorption. Eating and nutrient absorption can be restricted by:
Alcoholism is the number one cause of WKS because people who are alcoholics generally have a poor diet. Alcohol also prevents vitamin B-1 absorption and storage.
Lesions on the brain cause Wernicke’s disease (WD). These lesions are the result of a vitamin B-1 deficiency.
Prominent symptoms of WD are:
WD can later develop into Korsakoff’s syndrome. People who have WKS have a variety of issues relating to memory. You may suffer from memory loss or be unable to form new memories.
You may also have the following symptoms if you have WKS:
An individual with WKS is often mentally confused. This can make communication with the doctor difficult. Your doctor may overlook the possibility of a physical disorder if you’re confused.
Your doctor may first check for signs of alcoholism. They may check your blood alcohol levels. Sometimes, a doctor will take a liver function test to check for liver damage. Liver damage is a common sign of alcoholism.
Your doctor may also order nutritional tests to make sure you aren’t malnourished. Nutritional tests may include the following:
You may also need imaging tests. These tests can help your doctor find any damage that’s characteristic of WKS.
Diagnostic imaging tests for WKS include:
Your doctor may also use neuropsychological test to determine the severity of any mental deficiencies.
WKS treatment should begin immediately. Prompt treatment may delay or stop disease progression. Treatments are also able to reverse non-permanent brain abnormalities.
Treatment may first involve hospitalization. At the hospital, you’ll be monitored to ensure your digestive system is absorbing food properly.
The treatment for WKS may include:
In a small number of cases, treatment of vitamin B-1 deficiency produces a negative reaction. This is more common in alcoholics.
Negative reactions to receiving vitamin B-1 may vary. Reactions may include alcohol withdrawal symptoms like insomnia, sweating, or mood swings. You may also experience hallucinations, confusion, or agitation.
Dementia causes problems with thinking, memory, and reasoning. It happens when the parts of the brain used for learning, memory, decision making, and language are damaged or diseased.
Also called major neurocognitive disorder, it’s not a disease itself. Instead, it’s a group of symptoms caused by other conditions.
Alzheimer’s disease is the most common cause of dementia. Between 60% to 80% of people with dementia have Alzheimer’s. But there are as many as 50 other causes of dementia.
The symptoms of dementia may improve with treatment. But many of the diseases that cause dementia aren’t curable.
The most common causes of dementia include:
Dementia can be split into two groups based on which part of the brain is affected.
Some types of dementia affect both parts of the brain.
To treat dementia, doctors will treat whatever is causing it. About 20% of the causes of dementia are reversible.
Causes of dementia that may be reversible include:
These forms of dementia are partially manageable, but they aren’t reversible and get worse over time:
Usually, dementia goes through these stages. But it may vary depending on the area of the brain that is affected.
1) No impairment: Someone at this stage will show no symptoms, but tests may reveal a problem.
2) Very mild decline: You may notice slight changes in behavior, but your loved one will still be independent.
3) Mild decline: You’ll notice more changes in his thinking and reasoning. He may have trouble making plans, and he may repeat himself a lot. He may also have a hard time remembering recent events.
4) Moderate decline: He’ll have more problems with making plans and remembering recent events. He may have a hard time with traveling and handling money.
5) Moderately severe decline: He may not remember his phone number or his grandchildren’s names.He may be confused about the time of day or day of the week. At this point, he will need assistance with some basic day-to-day functions, such as picking out clothes to wear.
6) Severe decline: He’ll begin to forget the name of his spouse. He’ll need help going to the restroom and eating. You may also see changes in his personality and emotions.
7) Very severe decline: He can no longer speak this thoughts. He can’t walk and will spend most of his time in bed.
About 5% to 8% of adults over age 65 have some form of dementia. This percentage doubles every 5 years after 65. As many as half of people in their 80s have some dementia.
Patellofemoral arthritis is where there is degeneration and inflammation of the bone and cartilage at the patella (kneecap). It causes stiffness and pain at the front of the knee (anterior knee pain) and makes activities such as kneeling, climbing stairs, walking on slopes and getting up from sitting difficult and painful. It may develop gradually over time as part of aging or following an injury such as a fall or recurrent dislocations.
Here we will look at the different aspects of patellofemoral arthritis including what is going on in the joint, the common causes and symptoms, how it is diagnosed and the various treatment options, both surgical and non-surgical.
In patellofemoral arthritis, the cartilage on the back of the patella and in the trochlear groove become worn and inflamed. The cartilage thins and frays and if the wear and tear is severe it can expose the underlying bone. In an attempt to protect itself, the body may lay down extra layers of bone, known as bone spurs. The smooth surface is gradually lost leading to bone rubbing on bone. This can be painful and may limit movement.
In the picture here you can see changes that develop in patellofemoral arthritis. The LEFT image shows a normal knee – note the space between the kneecap and the femur. The MIDDLE image shows the loss of joint space due to arthritis. The RIGHT image highlights the bone spurs that form.
Patellofemoral arthritis may develop for a number of reasons:
1) Wear and Tear: Cartilage gradually thins as part of the normal aging process. Degenerative patellofemoral arthritis (known as osteoarthritis) usually affects those over the age of 65. Factors that increase the risk of developing arthritis include obesity, hip angle (which in turn affects knee position), gender (more prevalent in females), genetics and abnormal foot mechanics
2) Kneecap Injuries: Injuries to the kneecap such as fractures or dislocations can damage the cartilage on the patella which can lead to arthritis. Visit the kneecap injury section to find out more
3) Dysplasia: This is when the patella doesn’t sit properly in the trochlear groove, due to either the trochlear or the patellar being a slightly unusual shape, or tightness/laxity in the soft tissues affecting the angle that the patella sits at. As a result, when the knee moves there is excess stress, friction and/or pressure on the bones which can lead to patellofemoral arthritis
4) Medical Conditions: Certain medical conditions such as Gout or Paget’s disease increase the risk of developing patellofemoral arthritis.
The most common symptom of patellofemoral arthritis is anterior knee pain – pain at the front of the knee. The pain tends to be worse with activities that place pressure through the kneecap such as going up and down stairs, kneeling, squatting and getting up from a chair/bed.
Some people also experience crepitus, where they feel, or sometimes even hear, a cracking, grinding or popping sensation, when they move their knee. In severe cases when there is bone rubbing on bone, people may experience stiffness or the kneecap may get momentarily stuck, known as pseudolocking.
Treatment for patellofemoral arthritis usually starts with conservation i.e. non-operative, methods. In most cases, surgery is not required. Non-surgical treatments for patellofemoral arthritis include:
Avoid activities that aggravate symptoms as much as possible whilst still getting on with daily life. Use the hand rail when going up and downstairs, when sitting down or standing up take your weight through your good leg and if necessary use a stick or crutches when walking.
Non-steroidal anti-inflammatory medication (NSAIDs) such as ibuprofen or Advil may be prescribed to help reduce pain and inflammation.
Strengthening and stretching exercises help to improve the strength, stability and flexibility of the knee which can help to reduce the pressure on the kneecap and thus reduce pain – they are one of the most effective treatments for patellofemoral arthritis. A physical therapist will be able to give you a rehab programme to follow specific to your needs. Exercises that place pressure on the kneecap, such as squatting, should be avoided. Swimming is a good option as it strengthens the muscles without placing weight through the joint, or opt for cycling over running. Visit the knee exercises section for a whole range of exercises that can help.
Many people find that using either ice or heat helps to reduce pain and inflammation from patellofemoral arthritis. Ice has the added benefit that it helps to reduce inflammation – visit the ice wraps section to find out more.
Losing weight can make a difference, but is only appropriate if you are overweight. This will help to reduce the pressure going through the kneecap. Talk to your doctor or a dietician before starting on a weight loss programme to ensure it is suitable for you.
Corticosteroid injections can help to reduce patellofemoral arthritis pain and inflammation. However, they only help to treat the symptoms of arthritis, not the underlying cause so should be used alongside other treatment methods such as exercises or else the pain is likely to return. Find out more in the knee injectionssection
Wearing a knee brace or taping the patella can help to support the knee and change the position of the kneecap. Visit the knee braces section to find the right brace for you.
Glucosamine and chondroitin are popular supplements for reducing knee arthritis pain.
If moderate to severe symptoms of patellofemoral arthritis persist for more than 3-6 months of non-operative treatment, surgery may be advised. There are a few different options depending on the severity of the arthritis, which parts of the joint are affected and the age of the patient.
Suitable for mild to moderate patellofemoral arthritis. A chondroplasty is carried out arthroscopically (keyhole surgery). Small incisions are made around the kneecap through which thin surgical instruments and a small camera are inserted. Worn and frayed cartilage is trimmed and bone spurs smoothed out which both help to reduce friction in the joint.
This involves shifting the position of the tibial tuberosity – a small bony lump on the tibia (shin bone) where the kneecap attaches via the patella tendon. With this type of surgery, the tibial tuberosity is removed, repositioned and then reattached with anchors or screws. This makes subtle changes to the position of the knee cap improving the tracking of the patella, allowing it to glide more smoothly in the trochlear groove therefore resulting in less stress and friction on the arthritic parts of the patella. Tibial tuberosity transfer tends to be done in cases where patellofemoral arthritis affects only a portion of the kneecap, seeking to offload the arthritic parts.
Patella realignment surgery is done when tightness or laxity in the soft tissues means the patella doesn’t sit correctly in the trochlear groove which places excess pressure and friction on certain parts of the bone. With realignment surgery, the soft tissues around the kneecap are tightened or released to change the position of the patella in the trochlear groove. Examples of realignment surgery include lateral patellar retinaculum release, to release tight structures on the outer side of the kneecap, and reattachment or reconstruction of the medial patellofemoral ligament on the inner side of the knee.
With cartilage grafting, the damaged cartilage is replaced with healthy cartilage either from another part of the knee or from a tissue bank. If cartilage is being taken from the person’s own knee, two operations are required. The first is to harvest the cartilage from a non-weight-bearing part of the knee, which is then sent to a laboratory where cells are cultured for 3-6 weeks to increase the number of cartilage cells. In the second operation, the new cartilage cells are transplanted back into the affected parts of the patellofemoral joint. Cartilage grafting is usually done in younger patients in an attempt to delay the need for joint replacement.
With this type of partial knee replacement, the worn and damaged parts of the patellofemoral joint are removed and the surfaces re-lined with prosthetic implants. The trochlear groove is lined with a thin metal plate, and a plastic “button” is attached to the back of the patella – both components are fixed on using bone cement. Patellofemoral replacement is only suitable if the arthritis is confined to the patellofemoral joint – if other parts of the knee are also affected, a total knee replacement is needed. Patellofemoral replacement surgery tends to be most suitable for younger patients and has the advantage of being less invasive than a total knee replacement. People often report the knee feels more “normal” afterwards, most likely due to the fact that the knee ligaments are all preserved.
With a total or partial patellectomy, part or all of the patella is removed. It is only considered when there are no other options as whilst it may reduce pain, it inhibits the function of the quadriceps resulting in ongoing weakness.