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That Faecal Problem

Diagram of the Human Intestine.
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Sanitation in India has not kept up with the rest of our advances in the 21st century. We lack hygienic toilet facilities and 40 per cent of our population is forced to use open areas. This propagates a self-perpetuating cycle of diarrhoeal infections.

 

Most of the time, the diarrhoea settles in a day or two, with or without treatment. Sometimes, blood and mucous appear in the stool. This means that the diarrhoea has progressed to dysentery.

Often patients equate dysentery with amoebic infestation and the words ‘diarrhoea’ and ‘amoebic dysentery’ are interchanged. Most of the time they are right and the dysentery is due to the single celled amoeba Entamoeba histolytica. Around four per cent of the Indian population has antibodies to amoebae.

Amoebae have been around a lot longer than humans. They have perfected the art of survival. If exposed to extremes of temperature and medication, they can round themselves off into thick walled hibernating resistant cysts.

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Once the cyst is swallowed, amoebic dysentery sets in with an explosive onset of loose bloody stools, cramping abdominal pain and low grade fever. Many people recognise these symptoms, complain of “amoebic dysentery” and self medicate. They use single inadequate suppressant doses of medication. They may eventually become chronic carriers. In some, the amoebae burrow into the intestinal wall, causing perforations, and produce life threatening abscesses in the liver and the brain.

Treatment for amoebic infection is the “azoles” — metronidazole or secnidazole — followed by a second drug like diloxanide furoate. The duration of the treatment is around two weeks.

All dysentery is not caused by amoebae. Infections by other organisms can also produce blood and mucous in the stool. Some bacteria and viruses cause dysentery.

Symptoms of dysentery may occur without any infection at all. In people with diabetes, hypertension or abnormal disordered elevated lipids, the blood vessels supplying the intestine may be partially blocked. The intestine may get damaged in those areas, causing bloody and painful diarrhoea. The person may be diagnosed to have “repeated attacks of dysentery” and given inappropriate antibiotic treatment.

In older people the colon (or the large intestine) can get weakened in certain areas, causing finger-shaped small pouches called diverticula. Food can become trapped and remain in these areas. Inflammation and infection will produce symptoms similar to amoebiasis.

Cells can grow and bulge into the intestine, forming grape-like protrusions called polyps. These can cause recurrent attacks of bleeding from the rectum with or without diarrhoea. Cancers of the intestines can cause intermittent diarrhoea and dysentery.

A number of illnesses, loosely classified as inflammatory bowel diseases (IBD), are characterised by inflammation of various parts of the intestine. One of the common forms is ulcerative colitis that affects the large intestine. It causes intermit attacks of loose stool, with blood and mucous, accompanied by abdominal pain. Although there may be weight loss, many patients remain well between the attacks, giving an initial false impression of repeated attacks of amoebic dysentery. The exact cause of IBD isn’t known. Genes, heredity, environmental factors, stress and autoimmune diseases (where the body attacks its own cells) are all put forward as possible factors.

Milk allergy can cause diarrhoea. If the person is unaware of the condition and overloads the system, severe diarrhoea can result.

Sometimes the cause of the dysentery is obvious. It may follow treatment for cancer with radiation or medication. It can occur after prolonged courses of antibiotics. It may also be due to cancer of the intestines.

A single attack of dysentery may be “amoebiasis”, which can be cured by a complete course of medication. If the symptoms of the dysentery are recurrent, a correct diagnosis is essential. More so if a person over 30 years presents a sudden change in bowel habits or has alternating constipation and diarrhoea. The other danger signals for cancer are blood and mucous in the stool, poor appetite and weight loss.

Diarrhoea needs to be investigated if it lasts longer than two weeks, is recurrent, with blood and mucous in the stool, and there is weight loss.

To prevent infective diarrhoea
• Do not drink water that has not been boiled or purified
• Remember ice cubes in juice may be made from contaminated water
• Do not eat cut raw fruits or vegetables
• Eat food which is piping hot
• Always wash your hands before eating

Sources: The Telegraph (Kolkata, India)

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Mouth Or Dental Injury

Schematic of patterns of disease in Crohn's di...Image via Wikipedia

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Conditions that may increase the risk for problems after a mouth or dental injury:
.CLICK & SEE THE PICTURES

Many conditions, lifestyle choices, medicines, and diseases interfere with one’s ability to heal or fight infection. The person may be at risk for a more serious problem from his or her symptoms if he or she have any of the following. Be sure to tell the health professional in detail.

THE CONDITIONS:-

*Heart valve disease:

*Heart valve replacement

*Previous dental injuries

*Previous dental or gum surgery

*Radiation therapy to the mouth, face, or neck (now or in the past)

*Surgery to remove the spleen

Lifestyle choices:

*Alcohol abuse or withdrawal

*Drug abuse or withdrawal

*Smoking or other tobacco use

Medicines:

*Antiseizure medicines, such as phenytoin

*Birth control pills (oral contraceptives)

*Blood-thinning medicines, such as warfarin, heparin, and aspirin

*Calcium channel blockers, which are used to control high blood pressure or for people with heart problems

*Corticosteroids, such as prednisone

*Medicines that contain gold

*Medicines to prevent organ transplant rejection

*Medicines used to treat cancer (chemotherapy)

*Nonsteroidal anti-inflammatory drugs (NSAIDs), such as aspirin or ibuprofen

Diseases:

*Cancer

*Crohn’s disease

*Dental disease, such as tooth decay or gum disease

*Diabetes

*Eating disorders, such as anorexia nervosa or bulimia nervosa

*Gastroesophageal reflux disease

*Hemophilia

*Idiopathic thrombocytopenic purpura (ITP)

*Infection of the muscles and valves of the heart (endocarditis)

*Iron deficiency anemia

*Malabsorption syndromes

*Scleroderma

*Sickle cell disease

*Sjögren’s syndrome

*Vitamin deficiencies, such as too little folate, niacin, pyridoxine, riboflavin, vitamin C, and vitamin K
Credits

Sources:MSN Health & Fitness

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Ailmemts & Remedies

Growth Disorders

Overview:
Growth is one of the complex and amasing facts of life that most people take for granted, but it can be a cause for concern for parents who have a child who’s shorter than others of the same age and doesn’t appear to be growing any taller.

Children of the same age vary greatly in height due to factors such as diet, genetics, and ethnic background. In most cases, tall or short stature is not abnormal and is due to a family tendency to be taller or shorter than average or to reach final height later than usual. Tall or short stature is a cause for concern only if the child’s height is well outside the average range for his or her age. Abnormally short or tall stature may be caused by a number of disorders.

What are the types?
Normal growth depends on a nutritionally adequate diet and good general health and is controlled by specific hormones. disruption of any of these three important factors may lead to a growth disorder that results in a child having abnormally short or tall stature.
short stature:
A child may be shorter than normal if his or her diet is inadequate. a chronic illness, such as cystic fibrosis or severe asthma, may also result in poor growth. crohn’s disease, a type of inflammatory bowel disease, is another example of a chronic illness that may lead to short stature. babies who have intrauterine growth retardation may reach a shorter than average height i later life.

Sometimes, short stature is caused by insufficient production of the hormones that are necessary for normal growth. in some children, the pituitary gland does not produce enough growth hormone. insufficient production of thyroid hormones is another cause of poor growth.

short stature is also a characteristic feature of tuner syndrome, a genetic disorder that only affects girls. in addition, short stature may occur as a result of a skeletal abnormality such as achondroplasia, an inherited disorder in which the bones of the legs and arms are shorter than normal.

Tall stature:
children may be temporarily taller than others of the same age and sex if puberty occurs early. however, in such children, the final height is usually normal. in very rare cases, exaggerated growth caused by the overproduction of growth hormone results in excessive height known as gigantism. the overproduction may be due to pituitary gland tumor. boys with the chromosome disorder klinefelter syndrome may also grow taller than normal at puberty.

Causes of delayed growth:
There are a large number of medical, genetic and external factors that can delay or inhibit normal growth. These include conditions such as Growth Hormone Deficiency (GHD) in children, Turner’s syndrome, Down’s syndrome, achondroplasia (defective growth of cartilage cells in the bones of the limbs) and various malfunctions of the endocrine system.

Chronic diseases and illnesses can also have a detrimental effect on growth including Inflammatory Bowel Disease IBD, chronic renal insufficiency and heart disease, as too can factors such as malnutrition, drug and alcohol abuse, neglect, chronic stress and lack of exercise. However, in many cases the cause of delayed or restricted growth is not known.

Many children are smaller than average during childhood yet end up reaching a normal adult height. But for some, a more normal adult height will not be achieved without treatment with supplemental human growth hormone (hGH). These include children with GHD and Turner’s syndrome.
A more common growth disorder is growth hormone deficiency (GHD). This is the condition of having too little GH. There are several possible explanations for its occurrence:

You may click to see the pictures

A child can be born with GHD.
The condition also may arise because of damage to the hypothalamus or pituitary gland as a child or adult because of a tumor, an infection, or radiation to the brain — usually for the treatment of a tumor.
A deficiency in GH may also have an undefined cause. (In this case, it is said to be of idiopathic origin.)
Pituitary disorders, such as GH excess or GHD, are evaluated and treated by endocrinologists — medical specialists in hormone-related conditions. Because the diagnosis and treatment of such disorders require special expertise, primary care physicians who suspect patients have GH abnormalities should refer them to an endocrinologist.

One out of 2,500 to 5,000 children is born with a deficient growth hormone production resulting in impaired physical development, and another one in 2,000 to 2,500 girls are born with the genetic defect Turner’s syndrome. Both disorders may result in decreased final height, which may be improved by supplemental somatropin.

Growth Hormone Deficiency (GHD):-

In children
A child with an inadequate production of growth hormone (reduced or non-existent) may have a normal height and weight at birth, but the child’s physical development following birth is severely impaired.

The under-secretion of human growth hormone during childhood and puberty slows bone growth and teeth development, and also causes the growing plates of the long bones to close before normal height is reached. In addition, other organs of the body fail to grow and the body proportions remain childlike.

Without treatment the child with GHD risks the development of a range of complications, as well as having a short stature.

Turner’s syndrome
Turner’s syndrome is a common genetic defect that affects girls and women and occurs in about one out of every 2,000 to 2,500 female births.

In Turner’s syndrome all or part of one of the two X-chromosomes is missing, but the reason why this happens is not known. This defect can cause a number of physical and medical problems and in some cases creates educational and behavioural concerns.

Characteristics of Turner’s syndrome
As the extent of the defect to the chromosome varies, every case of Turner’s syndrome is individual and each affected girl may have only a few of the possible characteristics that can be associated with the syndrome.

Short stature is a common characteristic of Turner’s syndrome resulting in a decreased final adult height and is generally accompanied by a failure of the ovaries and infertility.

Growth failure in Turner’s syndrome
The reasons for the growth retardation in Turner’s syndrome are not entirely understood, but patients are generally not deficient in growth hormone. The pituitary gland produces adequate amounts but the long bones do not respond.

The growth plates appear to be resistant to the action of the body’s GH, yet the hormone functions normally in controlling metabolism and organ development. By treating with supplemental hGH the resistance can be overcome, creating growth in the long bones. Female hormones may need to be given as well.

Being a genetic problem the affected individual will be faced with the consequences of the syndrome all her life, but can expect to lead a healthy life with appropriate care and treatment.

Growth Hormone Excess:
Excess growth hormone (GH) in children (gigantism) is extremely rare, occurring in fewer than 100 children in the United States.

Excess GH in adults (acromegaly) most commonly occurs in middle-aged men and women. Approximately 60 out of every million Americans have acromegaly.

Very infrequently, GH excess may run in families, or be one manifestation of a number of rare syndromes.

Frequent Sign & Symptoms:

The signs and symptoms depends upon the type of growth disorder. A child with a growth problem needs to be evaluated by a health care provider to determine the underlying health issues involved.

How is it diagnosed?
Your child’s height will be measured during routine checkups. if his or her height is consistently either lower or higher than the normal range, he or she will need to be measured frequently. If growth rates continue to be normal, tests may be performed to check hormone levels and to look for underlying disorders, such as genetic abnormality. in some cases, maturity of a child’s bones may be assesses by taking x-rays of the hand and wrist.

What is the treatment?
Treatment for growth disorders is most successful if started well before puberty when bones still have the potential for normal growth. short stature caused by an inadequate diet usually improves if the diet is modified while the child is still growing. If the growth disorder is a chronic illness, careful control of the illness can sometimes result in normal growth. growth hormone deficiency is usually treated by replacement of growth hormone. hypothyroidism is treated by replacing thyroid hormone.

Abnormal early puberty may be treated using drugs to halt the advancement gland tumor may be treated by removal of the tumor.

Treated early, most children with a growth disorder reach a relatively normal height, but, if treatment is delayed until puberty, normal height is more difficult to achieve. Abnormal stature may cause a child to be self-conscious and unhappy, and he or she may need support such as counseling.

Growth Hormone Excess: Treatment Options
Because excess GH — acting alone or together with excess IGF-1 — produces adverse health effects, reducing the levels to normal is desirable. Surgery, medication and/or irradiation of the pituitary gland may be appropriate to achieve these goals.

Growth Disorders Lifestyle and Prevention:
For children:
Because growth hormone is taken for years, it is good for parents of children with GHD to be aware of some safety precautions:

Carefully follow the directions for taking GH
Tell all doctors who care for your child that he or she is taking growth hormone
Make sure your child takes any other prescription drugs exactly as prescribed
Contact your child’s doctor immediately if you have any questions about treatment or signs or symptoms which suggest a complication of GH treatment.
In addition, encourage your child to have a healthy lifestyle. Eating a variety of healthy foods will help your child to grow and respond to growth hormone treatment. Be sure that your child gets regular exercise and plenty of sleep, too.

For adults:

Adults receiving GH treatment should also eat a balanced diet, get regular exercise, and plenty of sleep.

Some adults find their lives are much better after taking GH alone. Others may find they still need some help, particularly with the psychological symptoms of GHD. You may need medication to control anxiety or lift your mood.

Counseling may be helpful too. Some forms of therapy, such as cognitive-behavior therapy, can allow you to correct negative thoughts you may be having. You also may want to join a support group with other adults who have GHD. Talking to others who have been through the same thing can be healing.

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://www.charak.com/DiseasePage.asp?thx=1&id=344
http://www.ferring.com/en/therapeutic/endo/About+Growth+Disorders/
http://www.hormone.org/Growth/overview.cfm

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Crohn’s Disease

 

Definition:
Crohn’s disease (also known as regional enteritis) is a chronic, episodic, inflammatory bowel disease (IBD) and is generally classified as an autoimmune disease. Crohn’s disease can affect any part of the gastrointestinal tract from mouth to anus; as a result, the symptoms of Crohn’s disease vary among afflicted individuals. The disease is characterized by areas of inflammation with areas of normal lining between in a symptom known as skip lesions. The main gastrointestinal symptoms are abdominal pain, diarrhea (which may be bloody, though this may not be visible to the naked eye), constipation, vomiting, weight loss or weight gain. Crohn’s disease can also cause complications outside of the gastrointestinal tract such as skin rashes, arthritis, and inflammation of the eye.

The disease was independently described in 1904 by Polish surgeon Antoni Lesniowski and in 1932 by American gastroenterologist Burrill Bernard Crohn, for whom the disease was named. Crohn, along with two colleagues, described a series of patients with inflammation of the terminal ileum, the area most commonly affected by the illness. Crohn’s disease affects between 400,000 and 600,000 people in North America. Prevalence estimates for Northern Europe have ranged from 27–48 per 100,000. Crohn’s disease tends to present initially in the teens and twenties, with another peak incidence in the fifties to seventies, although the disease can occur at any age.

Although the cause of Crohn’s disease is not known, it is believed to be an autoimmune disease that is genetically linked. The highest relative risk occurs in siblings, affecting males and females equally. Smokers are three times more likely to get Crohn’s disease.

Unlike the other major types of IBD, there is no known drug based or surgical cure for Crohn’s disease. Treatment options are restricted to controlling symptoms, putting and keeping the disease in remission and preventing relapse.

CLICK & SEE THE PICTURES
The three most common sites of intestinal involvement in Crohn’s disease are ileal, ileocolic and colonic.

Symptoms:
T the symptoms of crohn’s disease vary among individuals. The disorder usually recurs at intervals throughout life. Episodes of the disease may be severe, lasting weeks or several months before settling down to periods with mild or no symptoms. The symptoms include:

· Diarrhea.
· Abdominal pain.
· fever.
· Weight loss.
· General feeling of malaise.

If the colon is affected, symptoms may also include the following:

· Diarrhea, often containing blood.
· Bloody discharge from the anus.

About 1 in 10 people also develops other disorders associated with crohn’s disease. These other conditions may occur even in mold cases of crohn’s disease and include arthritis, eye disorders, kidney disorders, gallstones, and a rash.

Causes:
The exact cause of Crohn’s disease is unknown. However, genetic and environmental factors have been invoked in the pathogenesis of the disease. Research has indicated that Crohn’s disease has a strong genetic link. The disease runs in families and those with a sibling with the disease are 30 times more likely to develop it than the normal population. Ethnic background is also a risk factor. Until very recently, whites and European Jews accounted for the vast majority of the cases in the United States, and in most industrialized countries, this demographic is still true.

Mutations in the CARD15 gene (also known as the NOD2 gene) are associated with Crohn’s disease and with susceptibility to certain phenotypes of disease location and activity. In earlier studies, only two genes were linked to Crohn’s, but scientists now believe there are over eight genes that show genetics play a crucial role in the disease.

A handful of cases of Crohn’s disease cases were reported at the turn of the 20th century, but since then, the disease has continued to increase in prevalence dramatically. Some argue that this increase has been the result of a genetic shift in the population caused by conditions favoring individuals carrying the genes linked with the disease. These conditions could be a lower infant mortality rate or better health care in the nations that have the highest incidence of disease (industrialized nations).

Others argue that Crohn’s disease is caused by a combination of environmental and genetic factors. Many environmental factors have also been hypothesized as causes or risk factors for Crohn’s disease. Proven environmental risk factors include living in an industrialized country, smoking, and living in an urban area. Diets high in sweet, fatty or refined foods may also play a role. A retrospective Japanese study found that those diagnosed with Crohn’s disease had higher intakes of sugar, fat, fish and shellfish than controls prior to diagnosis. A similar study in Israel also found higher intakes of fats (especially chemically modified fats) and sucrose, with lower intakes of fructose and fruits, water, potassium, magnesium and vitamin C in the diets of Crohn’s disease sufferers before diagnosis, and cites three large European studies in which sugar intake was significantly increased in people with Crohn’s disease compared with controls. Certain chemicals in the diet, known as microparticles, are also hypothesized as a risk factor for the disease, as well as a poor imbalance of omega-6 to healthy omega-3 fatty acids that emerging research shows helps to improve all types of inflammatory disease. The most common forms of microparticles include titanium dioxide, aluminosilicates, anatase, calcium phosphate, and soil residue. These substances are ubiquitous in processed food and most toothpastes and lip glosses. Soil residue is found on fresh fruits and vegetables unless carefully removed.

Smoking has been shown to increase the risk of the return of active disease, or “flares”. The introduction of hormonal contraception in the United States in the 1960’s is linked with a dramatic increase in the incidence rate of Crohn’s disease. Although a causal linkage has not been effectively shown, there remain fears that these drugs work on the digestive system in similar ways to smoking.

Additionally, many in the scientific community believe that early childhood exposure to illness is necessary to the creation of a proper immune system for those with the genetic susceptibility for Crohn’s Disease. Higher incidences of Crohn’s Disease are associated with cleaner living conditions. Throughout the early and mid-20th century in the United States, the disease was strongly associated with upper-class populations, and today the disease does not yet exist in the many Third World countries, despite the fact that it occurs in all races. CD is also associated with first born and single children (because they would have less exposure to childhood illness from siblings) and in populations that have low incidences of gastric cancer. Gastric cancer is most often caused by the bacterium Helicobacter pylori that flourishes in cramped and unsanitary conditions.

Abnormalities in the immune system have often been invoked as being causes of Crohn’s disease. It has been hypothesized that Crohn’s disease involves augmentation of the Th1 of cytokine response in inflammation. The most recent gene to be implicated in Crohn’s disease is ATG16L1, which may reduce the effectiveness of autophagy, and hinder the body’s ability to attack invasive bacteria.

A variety of pathogenic bacteria were initially suspected of being causative agents of Crohn’s disease. However, the current consensus is that a variety of microorganisms are simply taking advantage of their host’s weakened mucosal layer and inability to clear bacteria from the intestinal walls, both symptoms of the disease. Some studies have linked Mycobacterium avium subsp. paratuberculosis to Crohn’s disease, in part because it causes a very similar disease, Johne’s disease, in cattle. The mannose bearing antigens, mannins, from yeast may also elicit pathogenic anti saccharomyces cerevisiae antibodies. Newer studies have linked specific strains of enteroadherent E. coli to the disease but failed to find evidence of contributions by other species.

Diagnosis:
The diagnosis of Crohn’s disease can sometimes be challenging, and a number of tests are often required to assist the physician in making the diagnosis. Even with a full battery of tests it may not be possible to diagnose Crohn’s with complete certainty; a colonoscopy is approximately 70% effective in diagnosing the disease with further being less effective. Disease in the small bowel is particularly difficult to diagnose as a traditional colonoscopy only allows access to the colon and lower portions of the small intestines; recent introduction of Capsule endoscopy aid in endoscopic diagnosis.

Endoscopy
A colonoscopy is the best test for making the diagnosis of Crohn’s disease as it allows direct visualization of the colon and the terminal ileum, identifying the pattern of disease involvement.

Radiologic Tests
A small bowel follow-through may suggest the diagnosis of Crohn’s disease and is useful when the disease involves only the small intestine. Because colonoscopy and gastroscopy allow direct visualization of only the terminal ileum and beginning of the duodenum, they cannot be used to evaluate the remainder of the small intestine.

CT and MRI scans are useful for evaluating the small bowel with enteroclysis protocols.They are additionally useful for looking for intra-abdominal complications of Crohn’s disease such as abscesses, small bowel obstruction, or fistulae. Magnetic resonance imaging (MRI) are another option for imaging the small bowel as well as looking for complications, though it is more expensive and less readily available.

Blood Tests
A complete blood count may reveal anemia, which may be caused either by blood loss or vitamin B12 deficiency. The latter may be seen with ileitis because vitamin B12 is absorbed in the ileum. Erythrocyte sedimentation rate, or ESR, and C-reactive protein measurements can also be useful to gauge the degree of inflammation.[48] It is also true in patient with ilectomy done in response to the complication. Another cause of anaemia is anaemia of chronic disease, characterized by its microcytic and hypochromic anaemia. There are reasons in anaemia, including medication in treatment of inflammatory bowel disease like azathioprine can lead to cytopenia and sulfasalazine can also result in folate malabsorption, etc. Testing for anti-Saccharomyces cerevisiae antibodies (ASCA) and anti-neutrophil cytoplasmic antibodies (ANCA) has been evaluated to identify inflammatory diseases of the intestine and to differentiate Crohn’s disease from ulcerative colitis.

Treatment:
Crohn’s is a chronic inflammatory disease of the bowel and treatment is focused on reducing inflammation. Treatment options include medications, nutritional supplements and surgery—either alone or in combination. Complementary and alternative treatments are used to help relieve symptoms in conjunction with other therapies. Treating Crohn’s disease effectively is complex – goals of therapy are to alleviate symptoms and to prevent flare-ups. It is important to develop a strong partnership with your gastroenterologist and nutritionist.

Medications: Aminosalicylates (sulfasalazine, mesalamine, balsalazide, and olsalazine) are given orally or rectally to reduce inflammation in the intestine. Corticosteroids (prednisone, methylprednisolone, hydrocortisone) reduce inflammation and are used short-term for acute flareups. Budesonide, one of a new class of nonsystemic steroids, targets the intestine rather than the whole body. Immunomodulators (azathioprine, 6-mercaptopurine, cyclosporine A, tacrolimus, methotrexate ), usually associated with organ transplants and used to decrease the risk of rejection. Increasingly, they’re being used to treat autoimmune diseases and used to treat people with Crohn’s disease. Usually prescribed for moderate to severe cases, immunomodulators are also used when fistulas develop or corticosteroids are no longer effective. Crohn’s is not caused by an infection, but antibiotics (metronidazole and ciprofloxacin) may help minimize symptoms and heal fistulas and abscesses. Biologics (infliximab (Remicade), adalimumab (Humira) are genetically engineered drugs that combat inflammation by neutralizing proteins in the immune system like tumor necrosis factor (TNF), which can cause inflammation. The advantage in using biologics is that they act selectively rather than suppressing the entire immune system.

Nutritional Support: Nutritional support for people with Crohn’s is a complex endeavor. Malnutrition is a common complication of the illness. Children need to increase their intake of calories and protein by as much as 150% of the recommended amounts for their age and height. It’s also important to increase fluids, proteins (especially fatty fish like tuna and salmon), complex carbohydrates, and potassium-rich foods like bananas, orange juice, potatoes and avocados. Supplements like fish oils, probiotics and liquid nutritional support (Ensure) may help, so be sure to consult your health professionals for the best plan for you or your child.

Complementary and Alternative Therapies:Many people are interested in nontraditional approaches to healing, especially when standard treatments produce intolerable side effects or aren’t able to provide an improvement. To address this interest, the National Institutes of Health established the National Center for Complementary and Alternative Medicine (NCCAM), which provides guidance and research.

Most complementary and alternative therapies don’t simply address a problem with the body. Instead, they focus on the entire person – body, mind and spirit. As a result, they can be especially effective at reducing stress, alleviating the side effects of conventional treatments and improving quality of life.

Studies have found that more than half the people with either Crohn’s disease or ulcerative colitis have used some form of complementary or alternative therapy. The most common complementary therapies tried were herbal and nutritional supplements, probiotics and fish oil. Side effects and ineffectiveness of conventional therapies are primary reasons for seeking alternative care. Only about two-thirds report their alternative or complementary therapy use to their doctors, however.

The majority of these therapies aren’t regulated as medications by the Food and Drug Administration. Manufacturers can claim that their therapies are safe and effective but don’t need to prove it. Because even natural herbs can have side effects and cause dangerous interactions, be sure to let your doctor know before you try any alternative or complementary therapies.

NCCAM’s findings are available on its Web site. You can also talk to information specialists at the center’s clearinghouse by calling 888-644-6226 between 8:30 a.m. and 5 p.m. Eastern time.

Moderate, regular exercise and stress management techniques like meditation, relaxation practices and cognitive therapy may help reduce the severity of symptoms.

Click to see also:>Alternative strategy better for Crohn’s Disease

Ayurvedic Recommended Therapy: Basti

Homeopathy – Crohn’s Disease And It’s Treatment…………..(1)…….(2)

Crohn’s Disease as related to Cat’s Claw

Lifestyle changes:
Certain lifestyle changes can reduce symptoms, including dietary adjustments, proper hydration and smoking cessation.

Surgery:
Most people with Crohn’s disease eventually need some type of surgery. Half of all children diagnosed with Crohn’s need surgery within 5 years. Surgery is used to remove damaged portions of the digestive tract or scar tissue or repair fistulas. Strictureplasty involves insertion of a ballon to widen narrow segments of intestine without having to remove any portion. Resection of the colon is done to remove damaged intestine. Subtotal colectomy removes part of the colon. Proctocolectomy removes the entire colon. An ileostomy is the creation of a stoma through which feces is passed and collected in a bag which must be emptied several times per day. Emergency surgery is sometimes required for bowel perforations, obstructions, intestinal bleeding, or severe fistulas.

Prospective Treatments:
Researchers at University College London have questioned the wisdom of suppressing the immune system in Crohn’s, as the problem may be an under-active rather than an over-active immune system: their study found that Crohn’s patients showed an abnormally low response to an introduced infection, marked by a poor flow of blood to the wound, and the response improved when the patients were given sildenafil.

Recent studies using helminthic therapy or hookworms to treat Crohn’s Disease and other (non-viral) auto-immune diseases seem to yield promising results.

A single, small, uncontrolled trial of patients with mild Crohn’s on stable medications suggested improvement with low dose naltrexone therapy.

Prognosis:
Crohn’s disease is a chronic condition for which there is currently no cure. It is characterized by periods of improvement followed by episodes when symptoms flare up. With treatment, most people achieve a healthy height and weight, and the mortality rate for the disease is low.

Crohn’s disease is a recurring disorder. Most affected people learn to live reasonably normal lives, but 7 in 10 people eventually need surgery. Complications and repeated surgery can occasionally reduce life expectancy. Crohn’s disease may increase the risk of colorectal cancer, and, for this reason, your doctor may advise you to have regular checkups that include colonoscopy.

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://www.healthline.com/humiracontent/crohn’s-disease-advanced-treatments
http://www.charak.com/DiseasePage.asp?thx=1&id=108
http://en.wikipedia.org/wiki/Crohn’s_disease
http://www.mayoclinic.com/health/crohns-disease/DS00104/DSECTION=11

Categories
Ailmemts & Remedies

Dyshidrosis

Definition:
Dyshidrosis, also termed Dyshidrotic Eczema, Pompholyx and Dyshidrotic Dermatitis, is a skin condition that is characterized by small blisters on the hands or feet. It is an acute, chronic, or recurrent dermatosis of the fingers, palms, and soles, characterized by a sudden onset of many deep-seated pruritic, clear vesicles; later, scaling, fissures and lichenification occur. Recurrence is common and for many can be chronic. Incidence/Prevalence is said to be 20/100,000 in the USA, however, many cases of eczema are diagnosed as garden-variety atopic eczema without further investigation, so it is possible this figure is misleading.
It is a non-contagious skin problem that is thought to be perhaps a reaction to some environmental irritant; it may also be an autoimmune disease. It is common, slightly more women get it than men, and has been one of the earliest known skin problems. It is rare in children under 10.

This condition is not contagious to others, but due to its unsightly nature can cause significant distress in regards to social interactions with others.

The name comes from the word “dyshidrotic,” meaning “bad sweating,” which was once believed to be the cause. Sometimes called pompholyx (Greek for “bubble”) which is generally reserved for the cases with blisters; in some countries, pompholyx refers to hand dyshidrosis.

……You may click to see the picture.

Symptoms:
Small blisters with the following characteristics:

*Blisters are very small (1 mm or less in diameter). They appear on the tips and sides of the fingers, toes, palms, and soles.

*Blisters are opaque and deep-seated; they are either flush with the skin or slightly elevated and do not break easily.
*Eventually, small blisters come together and form large blisters.

*Blisters may itch, cause pain, or produce no symptoms at all. They worsen after contact with soap, water, or irritating substances.

*Scratching blisters breaks them, releasing the fluid inside, causing the skin to crust and eventually crack. This cracking is painful as well as unsightly and often takes weeks, or even months to heal. The skin is dry and scaly during this period.

*Fluid from the blisters is serum that accumulates between the irritated skin cells. It is not sweat as was previously thought.

*In some cases, as the blistering takes place in the palms or finger. Lymph node swelling may accompany the outbreak. This is characterised by tingling feeling in the forearm and bumps present in the arm pits.

*Nails on affected fingers, or toes, may take on a pitted appearance.

Causes:
Causes of dyshidrosis are unknown. However, a number of triggers to the condition exist:

*Dyshidrosis has been historically linked to excessive sweating during periods of anxiety, stress, and frustration, however, many cases present that have no history of excessive sweating, and the hypothesis of dyshidrosis as a sweating disorder is largely rejected. Some patients reject this link to stress, though as a trigger of vesicular eruption it cannot be overlooked, as with other types of eczema.

*Vesicular eruption of the hands may also be caused by a local infection, with fungal infections being the most common. Sunlight is thought to bring on attacks, some patients link outbreaks to prolonged exposure to strong sunlight from late spring through to early autumn. Others have also noted outbreaks occurring in conjunction with exposure to chlorinated pool water or highly treated city tap waters.

*Soaps, detergents, fragrances and contact with fruit juices or fresh meat also can trigger outbreaks of dyshidrosis, as with other types of eczema.

*Systemic nickel allergies may be related such as foods high nickel content – cocoa, chocolate, whole grains, & nuts.

*Keeping skin damp will trigger or worsen an outbreak. For this reason, people with dyshidrosis should wear gloves, socks, and shoes made of materials which “breathe well”, such as cotton or silk. Certain fabrics may greatly irritate the condition, including wool, nylon and many synthetic fabrics.

*Inherited, not contagious. Often, patients will present with other types of dermatitis, such as seborrheic dermatitis or atopic eczema. For this reason, among others, dyshidrosis is often dismissed as atopic eczema or contact dermatitis.

*Can be the secondary effect of problems in the gut. Some sufferers claim diet can ease symptoms (relieving internal condition of IBS or intestinal yeast infection). Also Inflammatory bowel diseases of Ulcerative colitis and Crohn’s disease.

*Bandages, plasters or other types of skin-tapes may be irritating to dyshidrosis and should be avoided. As the skin needs to breathe, anything that encourages maceration of the palms should be avoided. If the ‘wounds’ are raw enough to warrant covering, pure cotton gloves or gauze should be used. Liquid Band-Aid brand bandage may be tolerated and helpful, refer to the Treatment section, below.

*Latex and vinyl gloves may increase irritation.

*Multiple Chemical Sensitivity

*Allergic reaction to Potassium Dichromate (leather preservative)

*Dyshidrosis can sometimes even be caused by dust mite allergies, with sufferers having to wash and change bedding weekly, sometimes even every 2 days or even every day, to combat symptoms.

*Balsam of Peru is a common irritant among sufferers of hand eczema, more commonly, people with dyshidrotic eczema.

Treatment:
There are many treatments available for dyshidrosis, however, few of them have been developed or tested specifically on the condition.

*Topical steroids – while useful, can be dangerous long-term due to the skin-thinning side-effects, which are particularly troublesome in the context of hand dyshidrosis, due to the amount of toxins and bacteria the hands typically come in contact with.

*Nutritional deficiencies may be related, so addressing diet and vitamin intake is helpful

*Hydrogen Peroxide – posited as a key alleviating treatment (not a cure) on a popular website, it is used in dilutions between 3% and 27% strength, but side-effects of its use include burning and itching, and there is argument as to whether it only attacks the ‘sick cells’.

*Potassium permanganate dilute solution soaks – also popular, and used to ‘dry out’ the vesicles, but can also be very painful and cause significant burning.

*Domeboro (OTC) helps alleviate itching in the short term.

*Emollients during the drying/scaling phase of the condition, to prevent cracking and itching. While petroleum jelly may work well as a barrier cream, it does not absorb into the skin and or allow it to breathe, so may actually be less helpful.

*Salt soaks

*White vinegar soaks

*Avoidance of known triggers – dyshidrosis sufferers may need to abstain from washing their own hair or bodies, or wearing gloves when they do so, however waterproof gloves are often potential irritants.

*Zinc oxide ointment

*Nickel-free diets

*When in the scaling phase of the condition, the scales may cause deep cracks and fissures in the skin. Filing (as with an emery board) may help to minimize this.

*Stress management counseling

*Light treatment: UVA-1, PUVA, Grenz rays, Low Level Light Therapy using a Red + NIR (LED) combination

*Ciclosporin a strong immunosuppressant drug used to combat dyshidrosis caused by ulcerative colitis

*Efalizumab (Raptiva) a medication used to treat psoriasis

*Tacrolimus and Pimecrolimus, potent immunomodulators often used to prevent organ rejection in topical, ointment form, may be used in severe cases.

*Unbleached cotton gloves may be used to cover the hands to prevent scratching and vulnerability of the skin to bacteria

*Plantain (Plantago major) infused in olive or other oil can be soothing.

*Band-Aid brand liquid bandage regularly applied during the (often painful) peeling stage allows the skin to breathe while protecting it from further irritation. Some suffers have found that with regular application the skin will close and reform within 1 to 2 days. Protection is sufficient that the user can (gently) wash their hands with no irritation, however additional application after each hand wash is suggested. It does not cure the condition and only aids healing during the peeling stage. Other spray-on or brush-on liquid bandaids can contain irritating ingredients and have not been found to be helpful, some will aggravate the condition significantly.

*Avoid metal computer keyboards and track pads which contain nickel.

Many sufferers of dyshidrosis will find that treatments that were previously suitable for them no longer work or have induced sensitive reactions, which is common in most types of eczema.

*It may be prudent to wear light cotton gloves while reading newspapers, books and magazines. The inks and paper may irritate the condition.
*Avoid Purell and other hand sanitizing products which contain alcohol. These may aggravate the condition.

*Wash affected hands and feet with cool water and apply a moisturizer as soon as possible.

*On the other hand, hot water usually kills the itch.

*Avoid moisturizers that contain water (cremes and lotions). Stick with ointments.

*Valium in small doses during flare ups
Click to learn more about Dyshidrosis and it’s proper treatment

ABC Homeopathy Forum for Dyshidrosis

Allergy testing:
Allergy testing is a contested subject among eczema communities. Some dermatologists posit that if a sufferer is allergic to a substance, then a general allergy test on the forearm will suffice, yet others believe that in conditions like dyshidrosis, the suspect substances need to be applied to the affected area to induce a reaction. -Often seen in people who are already suseptible to allergies and/or asthma.

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/Dyshidrosis
http://www.geocities.com/vyera/dyshidrosis/main.html

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