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CT Scan Scores Over Angiography

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A reports on a study that highlights the safety issues involved in detecting coronary blockages:-

Noninvasive CT scans are nearly as accurate at imaging coronary artery blockages as conventional angiography and are much safer for many patients, according to researchers who published a study released recently in the New England Journal of Medicine.

A CT scanner could eliminate the risks involved with traditional angiograms

.Angiograms are considered the gold standard for detecting blockages. But the procedure involves inserting a guide wire and catheter into the groin, threading them through the blood vessels to the heart and injecting a dye that allows the blockage to be seen in an X-ray.

Using a CT machine instead to make a three-dimensional image of the heart could eliminate the risks involved with traditional angiograms, including heavy bleeding, damage to blood vessels and even death, said Dr. Julie Miller, an interventional cardiologist at Johns Hopkins University School of Medicine in Baltimore and lead author of the study.

More than 1.2 million patients in the US undergo cardiac catheterisations each year, and 1-2 per cent of those cases result in complications, according to the American Heart Association. The National Center for Health Statistics at the Centers for Disease Control and Prevention estimates that about 25 people die each year as a result.

About 20 per cent to 30 per cent of those tests give patients a clean bill of health, and that means that hundreds of thousands of people are exposed to needless risk, Miller said. Many cardiologists see CT scans as a safer alternative because the scans are powerful enough to create a high-resolution image even when the contrast dye is administered by a simple intravenous line and thus more dilute.

Miller and her colleagues at nine hospitals in the US, Canada, Germany, Japan, Brazil, Singapore and the Netherlands identified 291 patients with symptoms of coronary artery disease who were candidates for traditional angiograms. Their median age was 59, and 74 per cent were men.

Before the patients had their angiograms, their hearts were imaged in 8.5 seconds with a 64-slice CT scanner made by Toshiba Medical Systems, which funded the study along with the National Institutes of Health and private foundations.

Two physicians examined each image and graded the degree of narrowing in 19 places in the main coronary arteries. Then the researchers compared the results from both procedures.

In the 163 patients with the highest degree of coronary artery disease — a narrowing of at least 50 per cent in at least one artery — the CT angiograms were 93 per cent as good as traditional angiograms, according to the study. Overall, the CT scans accurately identified 85 per cent of the patients who had the biggest blockages and 90 per cent of the patients who did not.

The researchers also found that 91 per cent of patients who were identified by the CT scans as having the most severe disease were correctly diagnosed, as were 83 per cent of patients whose scans did not reveal large blockages.

Two of the patients in the study had a reaction to the contrast dye used to perform the CT angiogram, and one patient died as a result of the conventional angiogram.

Dr. Matthew Budoff, director of cardiac CT at Harbor-UCLA Medical Center in Torrance, California, said the study confirmed results from his own research using a similar scanner made by General Electric Co. His study, funded by GE, was published this month in the Journal of the American College of Cardiology.

“It’s not quite but almost as good as an invasive angiogram,” said Budoff, who also receives speaking fees from GE. The CT test is faster and costs thousands of dollars less, and patients leave “with a Band-Aid and a bottle of water.”

“The benefits for many patients outweigh the risk of missing 1 per cent of disease,” he said.

But other doctors say that more data are needed to prove that CT angiograms are worthwhile, especially as a screening tool.

“What we really need is a study that compares cardiac CT to traditional ways of working up chest pain, like stress testing, and look at patient outcomes in both groups,” said Dr Rita Redberg, director of women’s cardiovascular services at University of California, San Francisco, Medical Center, who co-wrote a perspective article accompanying the study. “Without actual outcome data, we don’t know that this is going to help patients at all.”

Sources:Los Angeles Times

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Ailmemts & Remedies

Hamartomas

Definition:-
A benign (noncancerous) tumor-like growth consisting of a disorganized mixture of cells and tissues normally found in the area of the body where the growth occurs. It is focal malformation that resembles a neoplasm in the tissue of its origin. This is not a malignant tumor, and it grows at the same rate as the surrounding tissues. It is composed of tissue elements normally found at that site, but which are growing in a disorganized mass. They occur in many different parts of the body and are most often asymptomatic and undetected unless seen on an image taken for another reason.

CLICK & SEE THE PICTURES

Hamartomas result from an abnormal formation of normal tissue, although the underlying reasons for the abnormality are not fully understood. They grow along with, and at the same rate as, the organ from whose tissue they are made, and, unlike cancerous tumors, only rarely invade or compress surrounding structures significantly. The International Statistical Classification of Diseases and Related Health Problems (commonly known by the abbreviation ICD) is a detailed description of known diseases and injuries. … The following codes are used with International Statistical Classification of Diseases and Related Health Problems. … The International Statistical Classification of Diseases and Related Health Problems (commonly known by the abbreviation ICD) is a detailed description of known diseases and injuries. … The following is a list of codes for International Statistical Classification of Diseases and Related Health Problems. … Tumor (American English) or tumour (British English) originally means swelling, and is sometimes still used with that meaning.

A hamartoma, while generally benign, can cause problems due to their location. When located on the skin, especially the face or neck, they can be extremely disfiguring, as in the case of a man with a hamartoma the size of a small orange on his eyelid. They may obstruct practically any organ in the body, such as the eye, the colon, etc. They are particularly likely to cause major health issues when located in the hypothalamus, spleen or kidneys.

.Cowden syndrome
Cowden Syndrome or Cowden Disease is a serious genetic disorder characterized by multiple hamartomas. Usually skin hamartomas exist, and commonly (about 66% of cases) hamartoma of the thyroid gland exists. Additional growths can form in many parts of the body, especially in mucosa, the GI tract, bones, CNS, the eyes, and the genourinary tract. The hamartomas themselves may cause symptoms or even death, but morbidity is more often associated with increased occurrence of malignancies, usually in the breast or thyroid. Cowden syndrome is an inherited disorder characterized by multiple tumor-like growths called hamartomas, and an increased risk of certain cancers. …

Types:-

Lung
The most common hamartomas occur in the lungs. (Click to see different pictures of hamartomas in the lungs) About 5-8% of all solitary lung tumors, about 75% of all benign lung tumors, are hamartomas. They almost always arise from connective tissue and are generally formed of cartilage, fat, and connective tissue cells, although they may include many other types of cells. The great majority of them form in the connective tissue on the outside of the lungs, although about 10% form deep in the linings of the bronchii. They can be worrisome, especially if situated deep in the lung, as it is important and sometimes difficult to distinguish them from malignancies. An X-ray will often not provide definitive diagnosis, and even a CT scan may be insufficient if the hamartoma atypically lacks cartilage and fat cells. Lung hamartomas are more common in men than in women, and may present additional difficulties in smokers.

Some lung hamartomas can compress surrounding lung tissue to a degree, but this is generally not debilitative or even noticed by the patient, especially for the more common peripheral growths. They are treated, if at all, by surgical resection, with an excellent prognosis: generally, the only real danger is the inherent possibility of surgical complications.

Heart.
Cardiac rhabdomyomas are hamartomas comprised of altered cardiac myocytes that contain large vacuoles and glycogen. They are the most common tumor of the heart in children and infants. There is a strong association between cardiac rhabdomyomas and tuberous sclerosis (characterized by hamartomas of the central nervous system, kidneys and skin, as well as pancreatic cysts; 25-50% of patients with cardiac rhabdomyomas will have tuberous sclerosis, and up to 100% of patients with tuberous sclerosis will have cardiac masses by echocardiography. Symptoms depend on the size of the tumor, its location relative to the conduction system, and whether it obstructs blood flow. Symptoms are usually from congestive heart failure; in utero heart failure may occur. If patients survive infancy, their tumors may regress spontaneously; resection in symptomatic patients has good results.

Hypothalamus
One of the most troublesome hamartomas occurs on the hypothalamus. Unlike most such growths, a hypothalamic hamartoma is symptomatic; it most often causes gelastic seizures, and can cause visual problems, other seizures, rage disorders associated with hypothalamic diseases, and early onset of puberty. The symptoms typically begin in early infancy and are progressive, often into general cognitive and/or functional disability. Moreover, resection is usually difficult, as the growths are generally adjacent to, or even intertwined with, the optic nerve; however, the symptoms are resistant to medical control. Luckily, surgical techniques are improving and can result in immense improvement of prognosis.

...Click for Hypothalamic Hamartoma Treatment

Kidneys, spleen, and other vascular organs
One general danger of hamartoma is that they may impinge into blood vessels,(click to see different pictures of Kidneys, spleen, and other vascular organs Hamartoma). resulting in a risk of serious bleeding. Because hamartoma typically lacks elastic tissue, it may lead to the formation of aneurysms and thus possible hemorrhage. Where a hamartoma impinges into a major blood vessel, such as the renal artery, hemorrhage must be considered life-threatening.

Hamartomas of the spleen are uncommon, but can be dangerous. About 50% of such cases manifest abdominal pain and they are often associated with hematologic abnormalities and spontaneous rupture.

Angiomyolipoma of the kidney was previously considered to be a hamartoma or choristoma, but is now known to be neoplastic.

General danger of hamartoma is that they may impinge into blood vessels, resulting in a risk of serious bleeding. Because hamartoma typically lacks elastic tissue, it may lead to the formation of aneurysms and thus possible hemorrhage. Where a hamartoma impinges into a major blood vessel, such as the renal artery, hemorrhage must be considered life-threatening. Image File history File links Spleen. …

Hamartoma of the kidney is also called angiomyolipoma and can be associated with tuberous sclerosis. It is one of the more frequently seen hamartomas. The condition is more prevalent in women than men, and generally occurs in the right kidney. Hamartomas of the spleen are uncommon, but can be dangerous. About 50% of such cases manifest abdominal pain and they are often associated with hematologic abnormalities and spontaneous rupture. Angiomyolipoma is a benign renal lesion. … Tuberous sclerosis, (meaning hard potatoes), is a rare genetic disorder primarily characterized by a triad of seizures, mental retardation, and skin lesions (called adenoma sebaceum). …

Angiomyolipoma is not a hamartoma by definition, because fat and smooth muscles are not normal constituents of renal parenchyma. It is a Choristoma (microscopically normal cells or tissues in abnormal locations).

Cowden syndrome
Cowden syndrome is a serious genetic disorder characterized by multiple hamartomas. Usually skin hamartomas exist, and commonly (about 66% of cases) hamartoma of the thyroid gland exists. Additional growths can form in many parts of the body, especially in mucosa, the GI tract, bones, CNS, the eyes, and the genitourinary tract. The hamartomas themselves may cause symptoms or even death, but morbidity is more often associated with increased occurrence of malignancies, usually in the breast or thyroid.

Causes
Hamartomas result from an abnormal formation of normal tissue, although the underlying reasons for the abnormality are not fully understood. They grow along with, and at the same rate as, the organ from whose tissue they are made, and, unlike cancerous tumors, only rarely invade or compress surrounding structures significantly.

Prognosis
Hamartomas, while generally benign, can cause problems due to their location. When located on the skin, especially the face or neck, they can be extremely disfiguring, as in the case of a man with a hamartoma the size of a small orange on his eyelid. They may obstruct practically any organ in the body, such as the eye, the colon, etc. They are particularly likely to cause major health issues when located in the hypothalamus, spleen or kidneys.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.


Resources:

http://en.wikipedia.org/wiki/Hamartomas
http://www.nationmaster.com/encyclopedia/Hamartoma

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Child Epilepsy

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Definition:
Epilepsy is a nervous system condition that causes electrical signals in the brain to misfire. These disruptions cause temporary communication problems between nerve cells, leading to seizures. One seizure is not considered epilepsy — kids with epilepsy have multiple seizures over a period of time.

Epilepsy affects people in all nations and of all races. The onset of epilepsy is most common during childhood and after age 65, but the condition can occur at any age. Epilepsy is a condition of the nervous system that affects 2.5 million Americans. More than 180,000 people are diagnosed with epilepsy every year. In epilepsy, the normal pattern of neuronal activity becomes disturbed, causing strange sensations, emotions, and behavior or sometimes convulsions, muscle spasms, and loss of consciousness. These physical changes are called epileptic seizures Seizures occur when there’s a sudden change in the normal way your brain cells communicate through electrical signals. Seizures can be triggered in anyone under certain conditions, such as life-threatening dehydration or high temperature. Other types of seizures not classified as epilepsy include those caused by an imbalance of body fluids or chemicals or by alcohol or drug withdrawal. A single seizure does not mean that the person has epilepsy. EEGs and brain scans are common diagnostic test for epilepsy.

.…CLICK & SEE

Epilepsy:

* is not the only cause of childhood seizures
* is not a mental illness
* does not usually affect intelligence
* is not contagious
* does not typically worsen over time

Causes of Epilepsy

In about half the cases of epilepsy, there is an identifiable cause.The common Causes are:-

*Injury to baby during delivery

*Hydrocephalus-excessive fluid in the brain

*Delay in delivery with decreased oxygen supply to brain.

* infectious illness (such as meningitis or encephalitis)
* brain malformation during pregnancy
* trauma to the brain (including lack of oxygen) during birth or an accident
* underlying metabolic disorders

* brain tumors,tuberculosis, parasites in the brain

*Drugs e.g. pencillin chloroquine, medicines for depression, angina.

* blood vessel malformation
* strokes
* chromosome disorders

The other half of epilepsy cases are idiopathic (the cause is unknown). In some of these, there may be a family history of epilepsy — a child who has a parent or other close family member with the condition is more likely to have it too. Researchers are working to determine what specific genetic factors are responsible.

Symptoms :

Some Symptoms of Epilepsy :

* Seizures

*Fainting.

*Memory loss.

*Changes in mood or energy level.

*Dizziness.

*Headache.

*Confusion.
Understanding Seizures
Seizures vary in severity, frequency, and duration (they typically last from a few seconds to several minutes). There are many different kinds of seizures, and what occurs during one depends on where in the brain the electrical signals are disrupted.

click & see

The two main categories of seizures are generalized seizures, which involve the whole brain, and partial seizures, which involve only part of the brain. Some people with epilepsy experience both kinds.

Seizures can be scary — a child may lose consciousness or jerk or thrash violently. Milder seizures may leave a child confused or unaware of his or her surroundings. Some seizures are so small that only an experienced eye could detect them — a child may simply blink or stare into space for a moment before resuming normal activity.

During a seizure, it’s very important to stay calm and keep your child safe. Be sure to:

*Lay your child down away from furniture, stairs, or radiators.
*Put something soft under his or her head.
*Turn your child on his or her side so fluid in the mouth can come out.
*Never stick anything in your child’s mouth or try to restrain him or her.

Do your best to note how often the seizures take place, what happens during them, and how long they last and report this to your doctor. Once a seizure is over, watch your child for signs of confusion. He or she may want to sleep and you should allow that. Do not give extra medication unless the doctor has prescribed it.

Children who suffer from partial seizures may be frightened or confused by what has happened. Offer plenty of comfort and reassure your child that you’re there and everything is OK.

Most seizures are not life-threatening, but if one lasts longer than 5 minutes or your child seems to have trouble breathing afterward, call 999 for immediate medical attention.

Diagnosis
Talk to your doctor if your child has seizures, staring spells, confusion spells, shaking spells, or unexplained deterioration of school performance. The doctor can refer you to a paediatric neurologist, who will take a patient medical history and examine your child, looking for findings that suggest problems with the brain and the rest of the neurologic system.

If the doctor suspects epilepsy, tests will be ordered, which may include:

1) electroencephalography (EEG), which measures electrical activity in the brain via sensors secured to the scalp while the child lays on a bed. It is a painless test, which takes about 1 hour.
2) a magnetic resonance imaging (MRI) test
3) a computerised tomography (CT) scan, both of which look at images of the brain

Treating Epilepsy
Your doctor will use the test and exam results to determine the best form of treatment. Medication to prevent seizures is usually the first type of treatment prescribed for epilepsy management. Many children can be successfully treated with one medication — and if the first doesn’t work, the doctor will usually try a second or even a third before resorting to combinations of medications.

Although medications often work, if your child is unresponsive after the second or third attempts, it’s less likely that subsequent medications will be effective. In this case, surgery to remove the affected part of the brain may be necessary. Epilepsy surgery is done in less than 10% of seizure patients, and only after an extensive screening and evaluation process.

Additional treatments can be used for epilepsy that is unresponsive to medications. The doctor may implant a vagus nerve stimulator in the neck, or recommend a ketogenic diet, a high-protein, high-fat, low-carbohydrate diet that can be very successful in helping to manage seizures.

Even people who respond successfully to medication sometimes have seizures (called “breakthrough seizures”). These don’t mean your child’s medication needs to be changed, although you should let the doctor know when they occur.

Click to see Suppliment recomendations for Epilepsy

Living With Epilepsy
To help prevent seizures, make sure your child:

* takes medication(s) as prescribed
* avoids triggers (such as fever and overtiredness)
* sees the neurologist as recommended — about two to four times a year — even if responding well to medication

Keeping your child well-fed, well-rested, and non-stressed are all key factors that can help manage epilepsy. You should also take common-sense precautions based on how well-controlled the epilepsy is. For example:

* Younger children should have only supervised baths.
* Swimming or bike-riding alone are not good ideas for kids with epilepsy. A helmet is required for cycling, as for all kids.

With some simple safety precautions, your child should be able to play, participate in sports or other activities, and generally do what other children like to do. Teenagers with epilepsy will probably be able to drive with some restrictions, as long as the seizures are controlled.

It’s important to make sure that other adults who care for your child — family members, babysitters, teachers, coaches, etc. — know that your child has epilepsy, understand the condition, and know what to do in the event of a seizure.

Offer your child plenty of support, discuss epilepsy openly, and answer questions honestly. Children with epilepsy may be embarrassed about the seizures, or worry about having one at school or with friends.

Epilepsy (children) – newer drugs

Epilepsy – a parent’s guide

Seizures and Epilepsy

Helping Your Child Cope With Epilepsy

Fears over child epilepsy drugs

Parents to deal with Epilectic Chield

Resources:
http://www.charliebrewersworld.com/page4.htm
http://www-epilepsy.com/

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Legionnaires’ Disease

Definition:
Legionnaires’ disease, also known as Legionellosis, is a rare form of pneumonia.It takes its name from the first known outbreak which occurred in a hotel that was hosting a convention of the Pennsylvania Department of the American Legion in 1976...

CLICK & SEE THE PICTURES

Causes:

It is a type of pneumonia caused by bacteria. You usually get it by breathing in mist from water that contains the bacteria.The Legionella bacteria are found naturally in the environment, usually in water. The bacteria grow best in warm water, like the kind found in hot tubs, cooling towers, hot water tanks, large plumbing systems, or parts of the air-conditioning systems of large buildings. They do not seem to grow in car or window air-conditioners. The mist may come from hot tubs, showers or air-conditioning units for large buildings. The bacteria don’t spread from person to person.The disease is fatal in approximately 5% to 15% of cases.

CLICK & SEE..> :Legionella bacteria under the microscope

Symptoms:
Symptoms of Legionnaires’ disease include fever, chills, a cough and sometimes muscle aches and headaches. Other types of pneumonia have similar symptoms. You will probably need a chest x-ray to diagnose the pneumonia. Lab tests can detect the specific bacteria that cause Legionnaires’ disease.

The bacteria are more likely to make you sick if you:

* Are older than 65
* Smoke
* Have a lung disease
* Have a weak immune system

Legionnaires’ disease is serious and can be life-threatening. However, most people recover with antibiotic treatment. Legionnaires’ has an incubation period of between two and 10 days.
Initial symptoms of are similar to those of flu – headache, musclepain, and a general feeling of being unwell.These symptoms are followed by high fever and shaking chills. Nausea, vomiting, and diarrhoea may occur.On the second or third day, dry coughing begins and chest pain might occur. There may also be difficulty breathing.Mental changes, such as confusion, disorientation, hallucination and loss of memory, can occur to an extent that seems out of proportion to the seriousness of fever. Some patients may develop pneumonia. This could affect both lungs and lead to hospitalisation if severe.

Diagnosis:
Legionnaires’ disease is underreported and underdiagnosed, primarily because special tests are needed to distinguish Legionnaires’ disease from other types of pneumonia. To help identify the presence of legionella bacteria quickly, your doctor may use a test that checks your urine for legionella antigens — foreign substances that trigger an immune system response. You may also have one or more of the following:

* Blood tests
* A chest X-ray, which doesn’t confirm Legionnaires’ disease but does show the extent of infection in the lungs
* Tests on a sample of your sputum or lung tissue
* A CT scan of your brain or a spinal tap (lumbar puncture) if you have neurological symptoms such as confusion or trouble concentrating

Risk Factorts:

Legionnaires’ disease usually strikes middle-aged people. Those at risk include smokers and those with an existing health problem.Many others may contract the bug and yet show no signs of infection. It is likely that many cases of Legionnaires’ disease go undiagnosed.People suffering from cancer or chronic kidney diseases are among those less able to fight infections.Chronic diseases, such as diabetes and alcoholism, also seem to increase vulnerability to Legionnaires’ disease.Cigarette smokers are more likely to contract Legionnaires disease, perhaps because smokers are generally more likely than non-smokers to develop respiratory tract infections.

Treatment:

Legionnaires’ is most often treated with the antibiotic drugs erthryomycin and rifampin. Recovery often takes several weeks.

Prevention:

The likelihood of Legionella infection can be best reduced by good engineering practices in the operation and maintenance of air and water handling systems.Cooling towers and evaporative condensers should be inspected and thoroughly cleaned at least once a year.Corroded parts, such as drift eliminators, should be replaced. Algae and accumulated scale should be removed.Cooling water should be treated constantly. Ideally, an automatic water treatment system should be used that continuously controls the quality of the circulating water.Fresh air intakes should not be built close to cooling towers since contaminated water particles may enter the ventilation system.This page contains basic information. If you are concerned about your health, you should consult a doctor .

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

Resources:
BBC NEWS:8 Feb, 2003
http://www.nlm.nih.gov/medlineplus/legionnairesdisease.html
http://www.mayoclinic.com/print/legionnaires-disease/DS00853/METHOD=print&DSECTION=all

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Oh My Appendix!

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Human beings ate raw grass, leaves, bark and uncooked cereals, like rabbits and other herbivorous animals, before they became refined carnivores who cooked and softened their food. And like these animals, we too had a long appendix.

 click & see

As the nature of our diet changed, we did not require this organ and it eventually became small and rudimentary. It still nestles in the lower part of the right side of the abdomen, an appendage loosely attached to the transition point between the small and large intestines. The organ does not serve any discernible useful function. But in almost 40 per cent of the population it gives trouble at some time in their lives.

Digested food gets pushed in and out of the appendix during its transit through the intestine. As long as the opening remains patent, this does not pose a problem. Sometimes the opening of the appendix becomes narrowed and obstructed. This can occur because of intestinal worms, a hard stony piece of stool called a fecolith, or even undigested food particles. Contrary to popular opinion, orange pits and other swallowed seeds have not been shown to block the appendix.

The appendix is lined by abundant lymphoid tissue. This can swell and secrete infected fluid if there is a bacterial or viral infection. If this is sufficient to partially or completely block the opening, there is pain and swelling. If the symptoms are neglected, the appendix can “burst”, spilling the infection fluid into the surrounding area. The entire abdominal cavity can then become infected, causing peritonitis. The infection may get localised, forming an appendicular abscess.

Appendicitis initially produces non-specific symptoms like fever, vomiting, diarrhoea and abdominal pain. The pain may eventually localise in the lower part of the right side of the abdomen. There may also be acute pain in an anatomical area called McBurney’s point, situated a little away from the umbilicus.

The presentation of appendicitis may be atypical in the young (less than 10 years) and in the old (more than 60). The pain fails to localise in any particular area of the abdomen and may pose a diagnostic enigma. The symptoms may be confusing and the diagnosis missed if the appendix is situated in an abnormal location, too high, too low or at the back, or on the left side of the abdomen. Houdini, the magician, had an appendix on the left side. The diagnosis was missed and it perforated during a performance. He collapsed on stage, dying shortly afterwards.

Unfortunately, there are no confirmatory diagnostic blood tests for appendicitis as there are for other illnesses like typhoid or urinary tract infections. The suspicion of appendicitis can, however, become a certainty with an ultrasound or CT scan. But these procedures have an inherent latent period (waiting for the facility to become available) and the appendix can rupture in the interim.

Around 45 per cent of women are suspected to have appendicitis during their reproductive years. This is because the pain of appendicitis can be confused with tubal infection (salpingitis), urinary tract infection, ectopic pregnancy or even normal mittleschmerz, the mid-cyclic ovarian pain caused by rupture of the mature ovarian follicle and release of the ovum. In 30 per cent of surgeries, the diagnosis of appendicitis is wrong and a normal organ is removed. The mortality, however, is 50 per cent if the inflamed appendix is not treated surgically.

A laparoscopy clinches the diagnosis. The appendix itself can often be removed at the same time with a minimally invasive, no scar laparoscopic procedure, thus providing an investigation method that also cures. The appendix can also be removed through a classical incision.

Sometimes it is possible to control the infection with antibiotics, allowing the person to opt for an interval appendectomy at a convenient time. Some people have a “grumbling appendix” that causes repeated attacks of pain which can be managed conservatively. This delays the need for surgery. It is not a very wise course of action as the infection can flare up at inopportune moments. Women who have repeated attacks of appendicitis are also likely to develop adhesions and scars. This can distort the anatomy of the pelvic area and result in undesirable relative infertility.

Click to see also:->

Appendicitis

Sources: The Telegraph (Kolkata, India)

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