The post Ulcerative Colitis | Pictures, Causes, Symptoms, Diagnosis, & Treatments appeared first on Prime Health Channel.
]]>Ulcerative Colitis is a bowel disease that affects the colon or large intestine. It is also known as IBD (Inflammatory Bowel Disease) and incorporates a set of diseases affecting the gastrointestinal tract. It develops when the large intestine and rectum get inflamed resulting in tiny sores or ulcers on the colon lining. It starts in the rectum and spreads upwards involving the entire colon.
Inflammation induces bowel to move rapidly and discharge its contents quickly. Bowel lining has surface cells which die to form ulcers that release pus, mucus and also bleeding. It affects all ages, but mostly people between 15-35 age groups are diagnosed. UC have similar symptoms like irritable bowel syndrome and Crohn’s disease.
UC is a result of immune system failing to defend a bacteria or virus from inflaming intestinal walls. Other reasons are:
Symptoms get worse in the morning. However, it depends upon the bowel part affected.
UC is confused with other diseases due to similar symptoms and multiple tests will help experts to diagnose. The tests include:
In a standard surgery entire colon is removed and a small opening is left open at the end of the small intestine that forms ileostomy. Stool gets collected in the bag attached to the ileostomy. With recent improvements continent ileostomy is created from intestine that acts like a rectum and it is emptied regularly with a tube.
There is no evidence of what causes ulcerative colitis, but certain foods can worsen the situation. The following can help in preventing the disease to worsen:
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]]>The post Right Side Abdominal Pain | Causes, Symptoms, Diagnosis & Treatments appeared first on Prime Health Channel.
]]>The lower right part of the abdomen comprises of different organs like a colon (in case of men) and right ovary (in case of women). Many reasons can cause mild to serve pain in this area. In most cases, the pain which arises in the right lower abdomen is not a major concern as it may fade away on its own in a day or two. However, if the pain remains constant for few days, then it is recommended to go through a detailed check-up
The appendix is a thin and small tube located at the intersection of the small and large intestine. An inflamed appendix is defined as appendicitis and is supposed to be the most common cause.
Appendicitis is a serious condition wherein the doctors often recommend removal of the appendix through surgery. If left untreated, the appendix may rupture over time and cause other complications.
There are several other causes of pain on either side of the lower abdomen. It may also happen that the discomfort is experienced on the right side, but the cause of pain is on the left side. Some of the other causes have been listed below:
There are a few reasons that are specific to women and cause pain on the right side of the abdomen. These factors are usually more serious and require medical attention. Even though the pain may be felt on the lower right side of the abdomen, the pain may be arising from the left side. Some of the common causes include:
Similar to women, few causes are specific to men only. These conditions require immediate medical attention and two major reasons include:
The following symptoms are a cause for concern and require urgent medical attention:
It is important to consult a doctor when the pain in the lower right abdomen lasts for more than a few days.
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]]>The post Epigastric Pain | Causes, symptoms, diagnosis & Treatment appeared first on Prime Health Channel.
]]>Epigastrium lies in the upper abdomen precisely over the stomach. The epigastric region includes the stomach, a part of the liver, pancreas, and duodenum.
Epigastric pain occurs in the upper abdominal area just below the ribs. It occurs mainly when the gastric components tend to move upwards towards the back of the throat making a person feel a burning sensation and inflammation. The pain is usually felt while eating or right after eating or lying down immediately after eating. The nature of the pain might vary from mild to severe at times.
It is quite common in pregnant women as a result of increased pressure in the abdominal area and various hormonal changes that slow down the digestive process.
Different disease can cause this pain, so it becomes quite difficult to find out the exact reason behind it. But the common Aetiologies are the following-
The pain may come along with other symptoms of the underlying disorder or the original disease. But, it may involve other symptoms like:
A few cases of epigastric pain may be symptoms of an upcoming heart attack or other life-threatening hazards:
The doctor initially examines the patient’s history and conducts a physical examination along with a few tests to diagnose the actual cause:
A few cases of epigastric pain might not need any treatment if further complications do not occur. However, the treatment depends on the diagnosis and the underlying cause of the pain. The following might treat pains arising due to severe disorders:
A doctor must be called in for Epigastric pain, but a few methods can be tried at home to redeem the pain. The following are-
Epigastric pain although harmless in most cases may cause serious complications if the symptoms deteriorate. It results in discomfort while eating and can affect eating habits causing a weight loss. Some of these hazards include-
Epigastric pain does not usually cause such risks and might go away within an hour or two. But in serious cases, one must visit a doctor when the following symptoms are common:
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]]>The post Appendix Pain appeared first on Prime Health Channel.
]]>The appendix is a small, thin pouch and worm-like structure that is present in the colon and connected to the large intestine. It is anatomically termed as the vermiform appendix which means worm-like. The appendix is located in the lower part on the right-hand side of the abdomen and is usually a closed-ended, narrow tubular tissue, i.e., about 5-10 cm (approximately 4 inches long).
Appendix pain medically termed as appendicitis is a painful swelling of the appendix present in the cecum of the colon. If not appropriately treated on time, it might burst and be life-threatening. Pressing on that area, coughing or a walk may increase the pain making the situation worse. It can happen to any person at any point of time but is common more in men than women. Appendicitis occurs mostly between the ages of 10 to 30 years.
An appendix pain develops mainly in the middle of the abdomen which may appear and go but gradually moves to the lower part of the right-hand side of the abdomen. The pain becomes constant, and with time it becomes severe.
Appendicitis occurs due to blockage or any obstruction in the appendix due to a congregation of mucus or other parasites. It produces bacteria and rapidly multiplies as well as infects the intestinal wall. The growth of bacteria leads to inflammation and irritation causing pain that mostly begins in the middle of the abdomen that may appear or disappear at times. Other likely causes include:
Sometimes it becomes difficult to diagnose appendix pain as the symptoms are quite similar to many other abdominal diseases which include:
Also, due to its variation in size, location and being nearly located to other organs in the abdomen, it is tricky to differentiate appendicitis from other pelvic and abdominal issues. Some other conditions that may be confused with appendicitis are:
Some tests that are highly recommended for diagnosing appendix pain are:
At times, the appendix gets healed without surgery if the rupture happens with infection and inflammation. However, the symptoms may also go away with the use of antibiotics, especially in case of older people. As soon as the appendix gets diagnosed, it should be immediately removed by appendectomy to avoid the risk of an appendix burst. It is done under anesthesia either by a keyhole (laparoscopy) or open surgery. However, keyhole surgery is preferable as the patient recovers sooner than the open technique.
In case the lump or mass comprises of fatty tissue, it recovers and heals the issue on its own. However, if it is located during diagnosis, doctors might advise surgery wherein the patient is treated first with antibiotics and then operated a few weeks later. In some instances, the operation is not at all necessary, and the lump may disappear with medicines only.
After the surgery, you must keep an eye on the patient for various symptoms which are prone to cause further infection. They are as follows:
It is difficult to prevent appendix pain, but some foods may lower the risk. Intake of foods rich in fiber might lessen it. Fresh fruits and vegetables containing high fiber can help in preventing constipation and build up of stool which is the primary cause for appendicitis. Some high fiber items that may be helpful to avert it include:
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]]>The post Inflamed Colon appeared first on Prime Health Channel.
]]>Inflamed colon known as Colitis in medical terms is a disorder caused in the intestines (both large & small intestines) that cause abnormalities and bowel diseases.
A part of the gastrointestinal tract gets inflamed by this type of colitis. The tail end of the small intestine is mostly affected, but it can affect all the layers of the bowel. It causes inflammation and creates patches across different parts of the digestive tract.
It acutely affects the large intestine causing the lining of the colon to develop ulcers and sores that excrete pus and mucus at times. It causes inflammation in the intestine and abdominal discomfort. It also causes a continuous inflammation in one particular area and results to affect deeper into the intestine.
It occurs when the outer lining of the bowel pouches out through the layers of the spots present in the muscles of the intestinal wall. As a result of this, inflammation or infection is caused in the digestive tract. The small pores face obstruction from parts of stool and other infectious materials. The nearest tissue of the colon present on the left-hand side is inflamed and thereby causes pain and even fever. However, this can be treated by antibiotics. If not treated through medication, the condition worsens further leading to leakage of the colon and moreover blockage of the bowel. In that case, surgery is a must to remove the affected area of the intestine.
The colon usually consists of natural and healthy bacteria. Intake of antibiotics for treatment of any disease might kill these useful bacteria thereby allowing the other harmful bacteria to affect the colon causing inflammation. The most common type is named Clostridium difficile and it generates the disease called antibiotic-associated colitis. In case it is mild, it may be healed by taking metronidazole orally. In moderate cases, it can be treated by vancomycin which is also taken orally. But in acute conditions, the patient should be medicated with a mixture of oral vancomycin and metronidazole generated through a vein and vancomycin enemas. But when it comes to more severe issues such as bowel rupture, surgery is advised. Again, some complicated cases of this disease can be overcome by fecal pellets donated to the patient.
When chemicals get inserted into the colon, the colon gets inflamed, and major damages can occur. The mucosal lining of the colon might also get inflamed when reacted to strong chemicals.
Inflamed colon can also be the effect of intake of several medicines such as NSAIDs (nonsteroidal anti-inflammatory drugs), mycophenolate, ipilimumab and retinoic acid.
Colitis tends to occur more in younger people than the aged ones. The major causes are as follows:
Some tests and diagnostic methods are to be carried out, they include:
There is no immediate treatment for this, and the general procedure is to lessen the signs and symptoms. Doctors may suggest a drug therapy, and if not cured, the ultimate step is to undergo surgery. A few mild medicines may be prescribed.
Some common drugs that are used to reduce the symptoms are as follows:
If any of the following symptoms arise, a doctor must immediately be informed:
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]]>The post Collagenous colitis appeared first on Prime Health Channel.
]]>Collagenous colitis is an inflammatory disease of the colon, which is related with watery and chronic diarrhea, but without blood [1]. It is one form of microscopic colitis, the other being lymphocytic colitis.
The incidence is high in industrialized countries like United States, Canada, Europe, New Zealand and Australia. Estimates indicate that the incidence has increased from one to approximately 19 in every 100,000 individuals. The prevalence increases with age and peaks in people in their 70s [2].
These involve:
Such episodes may arise abruptly, without any apparent reason [3].
The exact causes are unclear [4]. As per some unproven theories, the underlying factors might be:
Around half of all sufferers can identify the particular time of occurrence of the first bout.
These involve:
Adults over 40 years of age are usually the most risk-prone. People suffering from an autoimmune disorder are also regarded as susceptible by doctors [5].
Diagnosis involves:
A series of diagnostic tests are often ordered to ascertain the exact cause/causes. These involve:
Biopsies of the colon should be examined under microscope to avoid misdiagnosis as irritable bowel syndrome (IBS) or lymphocytic colitis.
Despite multiple management and curative options being present, no single treatment option is regarded as effective for Collagenous colitis. Treatment only aims at reducing inflammation and diarrhea symptoms. Treatment options include:
These include:
Acidophyllus (found in yogurt), Florastor and Culturelle help restore the balance of beneficial bacteria inside the colon.
Although no specific diet is recommended, patients should avoid lactose or caffeine to avoid fluid secretion in the colon. Low-fat diets should be followed in the event of inability to digest fats.
Radical surgery (for colon removal and creating a diverting ileostomy) is a possible cure, but is mainly reserved for acute cases and is seldom recommended.
These include:
The possible complications include:
It is not life-threatening. However, there are cases that need intensive resuscitation – particularly those associated with vitamin deficiency, weight loss and acute dehydration.
Symptoms usually recur when treatment is slowed down. Most patients require continual therapy for management of the symptoms. The long term outcome varies, with some sufferers showing quick response and others taking time. There is also a waxing and waning period of symptoms. Continued treatment usually reduces problems.
Worsening of the symptoms can be prevented by measures like:
As the exact cause is unknown, the condition itself cannot be prevented.
Although often difficult to cure completely, Collagenous colitis can be managed with proper medical assistance as much as to make a better quality of life possible for sufferers.
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]]>The post Cyclic Vomiting Syndrome appeared first on Prime Health Channel.
]]>Cyclic Vomiting Syndrome (CVS) is a functional vomiting disorder characterized by cycles or episodes of acute nausea and vomiting that persists for several days or hours and alternate with asymptomatic episodes [1].
It is also called:
The exact prevalence and incidence of CVS is unknown. In a region in central Ohio with mainly white population, the prevalence of CVS in kids was found to be 0.04% [4].
The signs and symptoms include:
It may be characterized by either severe vomiting occurring several times every hour and lasting for less than a week, or 3 or more distinct episodes of vomiting without any apparent cause in the last 1 year.
It is typically characterized by fever, diarrhea, abdominal pain, dizziness and sensitivity to light.
The intervals between vomiting episodes are usually asymptomatic. However, some patients may suffer from the following problems between episodes:
Constant vomiting can result in severe dehydration which can be fatal for sufferers. The symptoms include:
The risk factors include:
Children with a family history of migraines are found to suffer from CVS when they get older. The relationship between CVS and migraines is not clear.
Chronic usage of marijuana (cannabis sativa) has also been linked with the development of CVS.
The exact causes of CVS are not known. The trigger factors for vomiting episodes are:
Identifying the trigger factors for CVS may help manage its symptoms.
Heredity (mitochondrial inheritance) is supposed to play a role in CVS development, as the disease is found to have a possible relationship with migraine. Single-base pair and rearrangements in mitochondrial DNA have been linked with these attributes.
Diagnosis can be difficult for CVS. Diagnostic procedure usually involves:
Diagnostic tests may involve:
However, there are no specific tests for CVS.
The essential diagnostic criteria for CVS include:
In order to avoid misdiagnosis, the differential diagnosis should include isolating the signs of CVS from those of:
There is no cure for CVS. Treatment aims at controlling the symptoms. Medications prescribed include:
Drugs used to manage migraine problems can sometimes prevent or stop cyclic vomiting episodes. The medicines may be recommended for frequent and chronic episodes.
Acute cases of dehydration may need treatment in hospital.
As per research, around half of all CVS sufferers have anxiety or depression. It is unclear to what extent anxiety and depression can result from, or cause, cyclic vomiting. Behavioral therapy (involving techniques and exercises) may be recommended for children suffering from anxiety or depression.
Home remedies for CVs include measures like:
These involve:
Stress, which can trigger vomiting bouts, can be managed by Biofeedback training.
However, none of these have been studied well.
The complications for CVS include:
Avoiding trigger factors can reduce the frequency of vomiting bouts. Prevention can also include lifestyle modification measures like:
CVS persists for an average span of 2- 2.5 years. It resolves in late childhood or during early teen years. A few patients continue to exhibit symptoms even when they turn into adults.
There is little evidence of mortality associated with CVS. However, acute cases of fluid loss can cause potentially fatal salt imbalances. During a CVS episode, blood pressure increases dangerously (hypertension). Severe dehydration due to CVS, that goes untreated, can also cause death.
Patients can get information and assistance from various support groups and online forums. These include (5):
National Organization for Rare Disorders
55 Kenosia Avenue
P.O. Box 1968
Danbury, CT 06813–1968
Phone: 1–800–999–6673 or 203–744–0100
Fax: 203–798–2291
Email: [email protected]
Internet: www.rarediseases.org
Cyclic Vomiting Syndrome Association
2819 West Highland Boulevard
Milwaukee, WI 53208
Phone: 414–342–7880
Fax: 414–342–8980
Email: [email protected]
Internet: www.cvsaonline.org
The ICD9 Code for CVS is 536.2 [3].
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]]>The post Short Bowel Syndrome appeared first on Prime Health Channel.
]]>Short Bowel Syndrome (SBS) is a condition characterized by malabsorption of nutrients which occurs as a result of surgical removal of the small intestine, or in some rare cases – due to complete dysfunction of major portions of the bowel. It is a rare condition caused by either acquired or congenital factors. It may affect both children and adults.
The condition is also referred to by other names, such as Short Gut Syndrome or simply Short Gut.
Studies on the incidence and/or prevalence of this condition are not easy to make due to its rarity. In the UK, the average number of patients was 2 in per million, based on the number of individuals requiring long term home parenteral nutrition. In Spain, the affected population was nearly 1.8 in per million (as recorded in 2002).
SBS can be caused by various acquired or congenital factors, which include:
The symptoms of SBS include:
SBS patients may also exhibit complications that are caused by insufficient absorption of minerals and vitamins, such as vitamins A, E, D, K and B12 as well as calcium, iron, magnesium, zinc and folic acid. These may give rise to symptoms of:
The following tests are normally conducted to detect whether or not a child or an adult is having this syndrome:
A number of conditions show signs and symptoms similar to that of SBS. Hence, while determining the presence of SBS, a doctor needs to differentiate it from these similar disorders. The differential diagnosis of SBS includes distinguishing its signs from those of other conditions such as:
A number of diseases are closely associated with SBS. These include the following:
At present, there are no definite curative options for SBS. Treatment for SBS is primarily aimed at relieving the symptoms. Prescription medications may be administered to manage the condition which includes:
The medications should also be accompanied by a high-calorie diet that supplies all the necessary minerals and vitamins as well as various types of fats, proteins and carbohydrates.
As the intestines of SBS patients are not able to absorb adequate amounts of nutrients, doctors may recommend administering intravenous or tube feeding. These procedures are:
Parenteral Nutrition involves administration of a specially-made nutritional formula directly into the patient’s bloodstream with the help of intravenous channels (IV). The formula is carefully prepared by the dietician to meet the specific energy needs of the patient. Delivering the nutrients straight to the bloodstream also allows to bypass the involvement of the digestive system altogether.
The special formula is generally administered daily over a course of 12-24 hours. If the patient requires a long-term PN support, the length of such a session will be reduced gradually.
In this procedure, the nutritional formula is administered through a tube. It is also referred to as tube feeding. This can be accomplished in two ways:
The decision to settle for surgical operation on a SBS patient requires fine judgment. A surgery is undertaken only after careful consideration and after all the other therapeutic options has been exhausted. Some patients may require operation due to the complications presented by stasis of the enteric contents, bacterial overgrowth and prolonged parenteral nutrition.
It is sometimes possible to use surgery to reshape the small intestine of patients to increase surface area of intestines and prolong the duration of time required for the food to pass through, thereby giving intestines more opportunity to extract nutrients.
Common surgical procedures to manage SBS include:
The STEP procedure was developed in early 2000s by MDs Tom Jaksic and Heung Bae Kim of the Children’s Hospital Boston. It involves lengthening of the bowel of patients which allows avoiding the necessity for intestinal transplantation. The process also creates a narrow space that allows the food to move through the digestive tract at an appropriate pace and carries bacteria and/or waste products out of the body.
The Bianchi procedure also lengthens the dilated bowel by cutting one half of the bowel and sewing it to the other half.
Patients who do not respond well to the above-mentioned treatment procedures might be required to undergo an intestinal transplant. A number of transplant types exist, which include:
SBS patients should avoid sodas, sugary desserts and fruit juices as these may increase the risk of diarrhea. Intake of salt may be increased depending on the status of the bowel. Diet for these patients depends on their condition. A diet with higher fat content is recommended for patients having 100 centimeters of jejunum intact, closing to nearly 50% or 60%. Carbohydrates should make up 20% to 30% of total daily calorie intake. Daily consumption of fibers should be limited to 15 grams or less. Lactose should be minimized or removed from diet if the patient is having lactose intolerance. The calcium levels should be kept at appropriate levels to lower the chances of Osteoporosis. An oral rehydration solution might be required due to difficulties in sodium absorption. The patient should also avoid bowel stimulants like alcohol and caffeine. The diet should also be supplemented by vitamin supplies. Chewing the food properly and adequately is necessary to facilitate nutrient absorption.
A number of complications might emerge from SBS. These include:
As there are no cures for this condition, survival of the patient and overall outcome may depend on a number of factors. The most common reason for death is liver failure which occurs after chronic hepatic parenchymal damage. The 4-year survival rate of newborn infants on TPN is approximately 70%. The 5-year survival rate is close to 20% in the same population with lower than 10% expected intestinal length. Many individuals die due to reduced venous access or severe septic complications. Pharmacological bowel compensation can help patients to avoid long term parenteral nutrition. Studies suggest that non-transplant surgical procedures can lead to clinical improvement of the condition in about 80% of patients. Early postoperative complications might lead to a higher mortality rate. However, 80% to 90% of patients who survive this critical stage are alive even after one year and almost 60% is alive after 4 years.
References:
http://www.patient.co.uk/doctor/Short-Bowel-Syndrome-%28SBS%29.htm
http://www.childrenshospital.org/az/Site1581/mainpageS1581P0.html
http://en.wikipedia.org/wiki/Short_bowel_syndrome
http://www.nlm.nih.gov/medlineplus/ency/article/000237.htm
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]]>The post Alcoholic Hepatitis appeared first on Prime Health Channel.
]]>It is an inflammatory condition or hepatitis of the liver that is caused by an excessive consumption of alcohol. The condition is frequently found in close association with hepatosteatosis, which is an early phase of alcoholic liver disorder. It may significantly contribute to the progressive development of fibrosis, which can ultimately lead to cirrhosis. Common symptoms of this condition include jaundice, fatigue, ascites and hepatic encephalopathy. The mild cases of this liver hepatitis are usually self-limiting. However, the severe cases carry a high mortality risk.
The ICD-9 Code for this disease is 571.1.
This form of hepatitis occurs when the liver is damaged due to excessive drinking of alcohol. The exact mechanism in which alcohol damages the liver and the reason why it affects only a small minority of regular heavy drinkers is not known. It is, however, clear that the process responsible for breaking down ethanol (the alcoholic compound present in wine, beer and liquor) produces highly toxic chemical substances like acetaldehyde. Chemicals like these trigger inflammations that destroy the liver cells. Web-like scars or small tissue knots develop over time that replaces the healthy liver tissue, thereby interfering with the natural functioning of the liver. This irreversible scarring, known as Cirrhosis, is the last stage of this alcoholic liver hepatitis.
Heavy consumption of alcohol can give rise to liver disorders, and the dangers increase with the total duration of time as well as the amount of alcohol consumed. However, as many heavy drinkers do not develop the symptoms of cirrhosis or alcoholic hepatitis in their entire lives, it is believed that certain other factors may play an important part as well. These include:
Individuals with increased body weight are found to be more prone to this condition.
Many heavy drinkers are actually malnourished people. This is either because they eat food poorly or that the alcohol and its harmful byproducts made it difficult for the body to absorb the food properly and break down its nutrients. This is especially so in case of certain vitamins, proteins and fats. Lack of nutrients caused by both these instances contributes to the cellular damage of the liver.
Mutations of certain genes can affect alcohol metabolism. This may increase the risk of developing an alcoholic liver disorder, along with other complications such as alcohol-related cancerous conditions. The exact genetic propensities have not been identified yet.
Presence of other forms of hepatitis can increase the risk of developing cirrhosis and liver hepatitis in a person if he or she is also found to be a heavy drinker. Hepatitis C greatly increases the risk of development of serious liver conditions.
Alcoholic hepatitis is not a viral condition and hence it is not contagious.
There are certain risk factors that might increase the chances of an individual of developing this disorder:
Some of the signs and pathological alterations, observed in liver histology, consist of:
The hepatocytes, under the influence of alcoholic change, frequently swell up with excess amounts of fats, proteins and water. All these proteins are generally exported into the bloodstream of an individual. Necrotic damage is accompanied by ballooning. The swelling can block the nearby biliary ducts, which leads to Diffuse cholestasis.
It is a condition that is characterized by accumulation of pre-keratin filaments in hepatocytes. Although this symptom is not exactly limited to the alcoholic liver disease, it is frequently a notable feature.
Necrotic changes trigger neutrophilic invasion as well as presence of the cellular debris within lobules. Generally, the Kupffer cells remove the quantity of debris. However they become overloaded in an inflammatory setting, thereby allowing the other white blood cells to get into the parenchyma.
The presence of chronic liver disease might indicate:
A number of different signs and symptoms are commonly associated with alcoholic hepatitis. This may include:
The cases of Alcoholic hepatitis may vary from being mild showing only liver enzyme elevations to severe liver inflammations that accompany development of jaundice, a prolonged prothrombin duration as well as liver failure. The severe instances are marked by either obtundation or dulled consciousness or a combination of prolonged prothrombin time and elevated bilirubin levels. In both of the severe categories, the mortality rate is 50% within the first 30 days from onset.
Other symptoms of the condition include:
Alcoholic hepatitis is different from cirrhosis that occurs as a result of long-term alcohol consumption. Patients having chronic alcoholic liver disorder and alcoholic cirrhosis might get affected by alcoholic hepatitis. The condition of Alcoholic hepatitis does not itself lead to cirrhosis. However, cirrhosis is more prevalent in patients who have been heavy drinkers of alcohol for a long time. Some alcoholic individuals develop the condition of acute alcoholic hepatitis as a sort of inflammatory reaction to cells that are affected by the fatty change. However, this is not something that is directly related to dosage of alcohol. Certain people seem to be more prone to have this reaction than the others. This is known as alcoholic steato necrosis.
The diagnosis of this disorder is made in patients with a history of chronic alcoholism who develops worsening results of liver function tests. This includes elevated bilirubin levels and aminotransferases. Ratio between aspartate aminotransferase and alanine aminotransferase (AST/ALT ratio) is generally 2 or more. Under most circumstances, the liver enzymes do not exceed that of 500. The alterations on a liver biopsy are vital in confirming clinical diagnosis of alcoholic hepatitis.
The various tests conducted to diagnose this condition include:
While diagnosing this disorder, physicians should rule out the presence of the following conditions that show symptoms similar to Alcoholic Hepatitis:
The treatment of this disease begins with the ceasing of alcohol consumption of the patient. Without it, other modes of curing the condition would not have any effect on the patient. According to the clinical practice guidelines recommended by American College of Gastroenterology, alcoholic hepatitis should be treated by administering corticosteroids. A Child-Pugh score or a MELD score should be used for risk stratification of the patients.
Patients with Hepatic encephalopathy or the ones showing a modified Maddrey’s discriminant function score greater than 32 should be treated with prednisolone 40mg tablets daily for 4 weeks which should be then followed by taper.
Randomized controlled trial indicated that patients showing at least 1 of the symptoms such as fever, palpable tender hepatomegaly, leukocytosis, hepatic systolic bruit or hepatic encephalopathy and having a discriminant function score greater than 32 should be treated with an oral dosage of pentoxifylline 400mg three times daily for four weeks in order to prevent death.
In cases of severe alcoholic hepatitis, a liver transplant surgery might be the only remaining option to evade death. The survival rates for a transplant are similar to that of the other types of hepatitis which is greater than 70% for 5-year survival.
However, most medical centers are somewhat reluctant to perform this transplant surgery as they fear that patients would resume their drinking habits once surgery is complete. For most alcoholic hepatitis patients, the disease itself is considered to be a contraindication for the liver transplantation procedure in most of the transplant centers of US.
Doctors might recommend certain dietary practices that patients might need to follow to reverse the nutritional deficiencies that accompany alcoholic hepatitis cases. A sufferer might also be directed to a dietician for assisting with his or her needs who may recommend an increased amount of vitamins or nutrients in the diet.
The following complications might result from Alcoholic hepatitis:
The long-term outcome for untreated cases of this condition is very severe. However, proper treatment and cessation of alcohol consumption can lead to a better recovery. If a patient of chronic alcoholic hepatitis continues to drink, he or she would inevitably develop symptoms of cirrhosis and liver failure. Death rate associated with alcoholic hepatitis is close to 50% within 7 years. Encephaylopathy, prolonged PT, PTT, kidney failure and ascites are promoting factors of liver failure. In some cases, death can also result from shock that is induced by the fat thrombosis within the lungs, very low levels of blood sugar or acute pancreatitis. Hence it is extremely important that a patient completely gets rid of his or her alcoholic tendencies if he or she has to have a positive outcome of treatment.
The following guidelines can help an individual to protect himself or herself from getting infected by this condition.
Severe cases of Alcoholic hepatitis might lead to death. Patients need to cease drinking alcohol immediately after diagnosis as this can help in survival and recovery.
References:
http://www.mayoclinic.com/
http://edition.cnn.com/HEALTH/
http://emedicine.medscape.com/
http://nyp.org/health/liver-
http://medical-dictionary.
http://www.liverfoundation.
http://www.fpnotebook.com/gi/
http://en.wikipedia.org/wiki/
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]]>The post Lymphocytic colitis appeared first on Prime Health Channel.
]]>Lymphocytic colitis is a rare disorder that is characterized by chronic episodes of non-bloody watery diarrhea. It is a subtype of an inflammatory bowel disease known as microscopic colitis, the other being collagenous colitis. In this condition, colonoscopy reveals normal features. However, mucosal biopsy shows accumulation of lymphocytes within colonic epithelium and lamina propria connective tissue.
People who are diagnosed with lymphocytic colitis mostly fall within the age group of 60 to 80 years. Women are slightly more inclined to develop this disease than men.
Medical experts are not sure as to what exactly causes this disease. However, some probable causes have been suggested which are discussed below:
Picture 1 – Lymphocytic colitis
The main symptom of the condition is chronic, non-bloody diarrhea. Individuals having this form of colitis can have watery diarrhea for many months or even years before a conclusive diagnosis is made. The symptoms normally begin very slowly and steadily which are intermittent with periods of well being, followed again by spells of chronic diarrhea. Bloody stool is not usual. The overall signs and symptoms experienced by patients of the condition include other signs and symptoms such as:
The diagnostic criteria used to determine if a patient is suffering from lymphocytic colitis is presented below:
When trying to determine if an individual has lymphocytic colitis, the doctor will first evaluate the complete medical history of the patient and conduct a thorough physical examination. He will then ask questions regarding any medications that the patient might be taking, such as ibuprofen and aspirin, which may increase the risks of developing this disorder.
Among the tests conducted to confirm the diagnosis is a stool sample test, which might help to rule out the possibility of infection as a cause of persistent diarrhea. Blood tests are carried out to test for other abnormalities that may indicate lymphocytic colitis. Biopsies are performed from different areas of the patient’s colon during a colonoscopy or a sigmoidoscopy which may reveal abnormalities in the colon lining such as patchy distributions. Multiple biopsies are required to be taken from various regions of colon so that an accurate diagnosis can be made. The patchy appearance of the disorder is also the reason why Flexible sigmoidoscopy is often inadequate in the diagnosis of this condition as the abnormalities might not be detected in sigmoid colon in around 30%-40% of cases. This deficit is rectified by colonoscopy which allows the doctor to obtain biopsies of the other regions that are inaccessible by sigmoidoscopy.
Lymphocytic colitis bears similarities to a lot of other health conditions in relation to their symptoms. Hence, a diagnostician needs to differentiate lymphocytic colitis from these conditions while confirming its presence. The differential diagnoses of the disease includes ensuring the absence of conditions like:
Treatment for this condition may vary depending on symptoms as well as the severity of an individual case. The condition may resolve on its own without any treatment. However, treatment becomes necessary if the symptoms grow more serious. Doctors generally proceed stepwise while trying to cure this condition, and start with the simplest and easiest treatments. Certain lifestyle changes may be recommended to manage the condition. These might include following some dietary regulations and avoiding pain relievers like ibuprofen and aspirin. If these changes are not enough, a doctor can recommend the following medications:
Picture 2 – Lymphocytic colitis Image
The medications that help in controlling diarrhea include bismuth subsalicylate (Pepto-Bismol), loperamide (Imodium A-D), as well as combination of atropine and diphenoxylate (Lomotil).
These help in reducing inflammations. A corticosteroid drug like budesonide or prednisone can control inflammations of the colon.
Cholestyramine can absorb bile acids and reduce the diarrhetic symptoms.
Medications like mesalamine (Pentasa, Asacol) and sulfasalazine (Azulfidine) can help to control colon inflammations.
These aid in reducing colon inflammation and include medications like azathioprine (Imuran, Azasan) and methotrexate (Rheumatrex).
If the symptoms of the disorder progress to a severe stage and medications are not effective enough, a doctor might recommend Colectomy – a surgical procedure in which all or a part of the colon is removed. Surgeries are rare for these disorders and should be opted for only when all other treatment methods have been tried out.
Apart from taking the medications as prescribed by the doctor, the treatment of lymphocytic colitis also involves following a strict diet plan that will restore balance and create less pressure in the colon. An ideal diet plan for patients, which includes providing nutrition and making sure that the symptoms do not aggravate, is presented below:
If left untreated, the disease may progress and result in any or all of the following complications:
The outcome of the disorder often depends on the severity of the symptoms. Nearly 20% of patients might experience spontaneous remission without any specific treatment. More than 50% of patients undergoing therapy have shown significant signs of improvement with reduced symptoms after only 6 months, whereas 15% of patients demonstrated signs and symptoms that were persistent. The symptoms of diarrhea may come and go over many years in certain patients. However, 80% or more patients have said that their symptoms of diarrhea along with histological abnormalities have resolved within 3 years. The condition does not result in colon cancer.
Lymphocytic colitis should be treated with medications and a proper diet plan to obtain optimum results.
References:
http://surgpathcriteria.stanford.edu/gi/lymphocytic-colitis/
http://www.mayoclinic.com/health/collagenous-colitis/DS00824
http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Collagenous_colitis
http://emedicine.medscape.com/article/180664-overview
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