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         Portal-systemic Encephalopathy:     more detail
  1. Chronic portal-systemic encephalopathy: An experimental study with special reference to brain serotonin (Bulletin No. 66 from the Department of Surgery, Lund University) by Finn Bengtsson, 1987

21. Clinical Nuclear Medicine - UserLogin
In portalsystemic encephalopathy, the presence of basal ganglia lesions with Tc-99m HMPAO; Cerebral Blood Flow; portal-systemic encephalopathy; SPECT
http://www.nuclearmed.com/pt/re/cnm/fulltext.00003072-199809000-00025.htm
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22. Clinical Nuclear Medicine - Abstract: Volume 23(9) September 1998 P 634-636 Tc-9
Perfusion SPECT Images in a Patient with portalsystemic encephalopathy. reported reduced cerebral blood flow in portal-systemic encephalopathy.
http://www.nuclearmed.com/pt/re/cnm/abstract.00003072-199809000-00025.htm
LWWOnline LOGIN eALERTS REGISTER ... Archive Tc-99m HMPAO Brain Perfusion SPECT... ARTICLE LINKS:
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Permissions Tc-99m HMPAO Brain Perfusion SPECT Images in a Patient with Portal-Systemic Encephalopathy.
Clinical Nuclear Medicine. 23(9):634-636, September 1998.
OHTA, HITOYA M.D.; MATSUMOTO, RIKI M.D.; KATO, TOMONOBU M.D.; TOMONO, NAOMI M.D.; SHIMIZU, TATSUO M.D. Abstract:
Tc-99m HMPAO SPECT brain perfusion was performed in a patient with portal-systemic encephalopathy. Decreased perfusion to both parietal lobes and increased perfusion to the basal ganglia bilaterally were demonstrated. After successful treatment, these findings improved. Some authors have reported reduced cerebral blood flow in portal-systemic encephalopathy. However, to our knowledge, there have been no reports describing a case in which both increased perfusion and decreased perfusion are recognized simultaneously.
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23. Hepatitis Central, References, Subclinical Hepatic Encephalopathy Impairs Daily
Pathogenesis and treatment of portalsystemic encephalopathy an update. Dig DisSci 1992; Gitlin N. Subclinical portal-systemic encephalopathy.
http://hepatitis-central.com/hcv/symptoms/encephalopathy/references.html
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    The study also found that substance-using MSM are at high risk of both HIV and hepatitis C infection. Little is known about the intersection of risk behaviours of MSM with substance use in Asia. Should Children Be Vaccinated Against Hepatitis A?
    ... Should Children Be Vaccinated Against Hepatitis A?POSTED: 2:58 pm EDT September 1, 2005UPDATED: 4:53 ... your child be vaccinated against hepatitis A?An editorial in 'The New ... GSK launches its second anti-hepatitis B drug in China
    ...extract unavailable

    24. Blackwell Synergy - Cookie Absent
    METHODS Twentyfive patients with portal-systemic encephalopathy were The data suggested that chronic portal-systemic encephalopathy results when a
    http://www.blackwell-synergy.com/doi/abs/10.1111/j.1572-0241.2005.40559.x
     Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

    25. CCHS Clinical Digital Library
    Encephalopathy, Hepatic Access document; portalsystemic encephalopathy Accessdocument; Hepatic Failure Access document
    http://cchs-dl.slis.ua.edu/clinical/gastroenterology/hepatic/hepatic/hepatic_enc
    Clinical Resources by Topic: Gastroenterology
    Hepatic Encephalopathy Clinical Resources
    Emergency Pediatrics Pathology Clinical Guidelines ... Miscellaneous Resources See also:

    26. Portal Toolkit Invalid Site URL
    portalsystemic encephalopathy may be seen with hyperammonemia that complicates portal-systemic encephalopathy is the most commonly encountered form of
    http://ppv.ovid.com/pt/re/obes/fulltext.00000132-200103000-00010.htm
    Sorry, the URL specified, http://ppv.ovid.com:80/pt/re/obes/fulltext.00000132-200103000-00010.htm , is invalid.

    Thank you

    27. Chapter 2 - Section 6: First Principles Of Gastroenterology
    The treatment of portalsystemic encephalopathy includes dietary protein restriction.Management will obviously need to be individualized for patients with
    http://gastroresource.com/GITextbook/En/chapter2/2-6.htm
    - Select a chapter - 1. Symptoms and Signs 2. Nutrition 3. Ethics 4. Research/Clinical Trials 5. Esophagus 6. Stomach and Duodenum 7. Small Intestine 8. Intestinal Ischemia 9. H.I.V. 10. Inflammatory Bowel 11. Colon 12. Pancreas 13. Biliary System 14. Liver 15. Paediatrics 16. Video Endoscopic Images Search
    Chapter 2:
    Nutrition Sections:
    1. Introduction 2. Essential Pysiologic Concepts in Nutrition 3. Clinical and Laboratory Features of Protein-Energy Malnutrition 4. Effects of Malnutrition on the Gastrointestinal Tract and Pancreas ...
    Acknowledgements

    6. Dietary Therapy in Liver Disease page 65 Two important manifestations of chronic liver disease, ascites and portal-systemic encephalopathy, can be effectively treated with dietary modifications. The prime dietary objective in the treatment of ascites is sodium restriction. Some authorities have recommended restriction of dietary sodium intake to as little as 10-20 mmol/day for patients with symptomatic, large-volume ascites. However, it is almost impossible to design a palatable diet or provide sufficient protein to maintain nitrogen balance with such stringent restrictions, and therefore these will not be satisfactory for long-term use. Well-motivated patients can often be maintained on a 40 mmol sodium diet (equivalent to about 1 g of sodium or 2.5 g of sodium chloride). TABLE 8. Diet therapy for hereditary liver diseases

    28. Gastroenterology Chapter 2 Nutrition In Gastrointestinal Disease
    portalsystemic encephalopathy. Answer (steatorrhea section 5.1, p61; celiacdisease section 5.2, p62; inflammatory bowel disease section 5.3, p63;
    http://gastroresource.com/GITextbook/en/chapter2/workbook-pr.htm
    Chapter 2 Workbook
    LEARNER OBJECTIVES At the completion of this chapter, the learner will be able to: Section 2: Essential Physiologic Concepts
    2.1 Describe the essential physiologic concepts in nutrition.
    2.2 Identify hormonal regulation of nutrition metabolism by:
      a. Listing the regulatory hormones
      b. Describing each regulatory hormone's metabolic action
    Section 3: Clinical and Lab Features of Protein-Energy Malnutrition
    3.1 Identify the clinical and laboratory features of protein-energy
    malnutrition, including causes and clinical features.
    Section 4: Effects of Malnutrition on GI Tract and Pancreas
    4.1 Describe the effects of malnutrition, including both structural and
    functional changes, on the gastrointestinal tract and pancreas. Section 5: Dietary Therapy in GI Disease 5.1 List the general principles of dietary therapy for:
      a. Celiac disease b. Inflammatory bowel disease
    Section 6: Dietary Therapy in Liver Disease 6.1 Discuss appropriate dietary therapy for:
      a. Ascites b. Portal-systemic encephalopathy

    29. World J Gastroenterol
    METHODS Twentynine patients with portal-systemic encephalopathy due to portalhypertension were classified by West Haven method into grade I(29 cases),
    http://www.wjgnet.com/1007-9327/abstract_en.asp?f=1939&v=10

    30. World J Gastroenterol
    METHODS Twentynine patients with portal-systemic encephalopathy due to portal portal-systemic encephalopathy is a kind of syndrome caused by portal
    http://www.wjgnet.com/1007-9327/10/1939.asp

    31. Cirrhosis
    Lactulose in the treatment of chronic portalsystemic encephalopathy. N Engl JMed 1969; 281 408-12. PubMed. 12 Simmons F, Goldstein H, Boyle JD.
    http://janis7hepc.com/cirrhosis22.htm
    Home Cirrhosis Back to Main Cirrhosis Page 2005 Research 2004-2001 Research Archives Dispelling myths in the treatment of hepatic encephalopathy Debbie Shawcross, Rajiv Jalan Lancet 2005; 365: 431-33 Institute of Hepatology, University College London, London WC1E 6HX, UK (D Shawcross MRCP, R Jalan, FRCP) Context Guidelines for the treatment of hepatic encephalopathy suggest ammonia reduction as the main focus, based on strategies to reduce ammonia's generation and absorption in the colon by using lactulose and a reduced protein diet. Starting point Two studies provide compelling and provocative data questioning the relevance of these interventions. Bodils Als-Nielsen and colleagues, in a systematic review of randomised trials, found insufficient evidence about whether non-absorbable disaccharides are beneficial ( BMJ 2004; 328: 1046-50). In a small randomised study, Juan Cordoba and colleagues showed that diets with normal protein content can be administered safely during episodic hepatic encephalopathy due to cirrhosis and that protein restriction does not have any beneficial effect during such episodes ( J Hepatol Where next Two approaches to new therapies for hepatic encephalopathy are needed. First, it is important to focus on the interorgan metabolism of ammonia. The small intestine and kidneys might be important producers of ammonia, and muscle is an important organ that can remove ammonia. Novel therapies targeting these organs reduce ammonia. Second, research is needed to explore factors other than ammonia that might be important in hepatic encephalopathy, including the synergistic role of inflammation. The lack of conclusive data about the efficacy of any treatment supports the view that placebo-controlled trials of newer agents are needed and ethical. The emphasis should shift to aggressive management of the precipitating event.

    32. Cirrhosis
    portalsystemic encephalopathy (PSE). Fetor hepaticus is caused by the portal-systemic encephalopathy by Sanjay Sandhir, MD, Frederick L. Weber, Jr, MD,
    http://janis7hepc.com/cirrhosis3.htm
    Home Cirrhosis Back to Index 2005 Research 2004-2001 Research Archives PHYSICAL FINDINGS SUGGESTIVE OF CIRRHOSIS A liver biopsy is the only definitive test that actually indicates whether or not you have cirrhosis [irreversible scaring of the liver]. So, what exactly is your doctor looking for when he/she does a physical exam? Are there actually some physical clues that suggest that you have cirrhosis? The answer to this question is yes. The following is a list of clues that indicate that you may already have cirrhosis. These are listed alphabetically by their common medical name. It is important to remember that, although helpful, each of these physical manifestations do not indicate the actual cause of one's liver disease, and, in fact, are not specific only to liver disease. They can be due to other disorders as well. ASCITES An accumulation of excess fluid in the abdomen. Causes abdominal distention. Can be treated with a low sodium diet, and the use of diuretics, i.e. water pills. Ascites:
    The two most important factors in the development of ascites are failure of the liver to synthesize albumin and portal venous hypertension.

    33. IngentaConnect Table Of Contents: Metabolic Brain Disease
    Proton Magnetic Resonance Spectroscopy in portalsystemic encephalopathy Role of Manganese in the Pathogenesis of portal-systemic encephalopathy
    http://www.ingentaconnect.com/content/klu/mebr/1998/00000013/00000004

    34. Healthnotes
    significantly improved portalsystemic encephalopathy (PSE).37 A second in chronic portal-systemic encephalopathy a randomized controlled trial.
    http://www.safeway.com/wellness/healthnotes.asp?org=safeway&ContentID=1231004

    35. Hepatic Encephalopathy: Definition And Much More From Answers.com
    portalsystemic encephalopathy n. Encephalopathy associated with cirrhosis ofthe liver, attributed to the passage of toxic nitrogenous substances.
    http://www.answers.com/topic/hepatic-encephalopathy
    showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Medical Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Hepatic encephalopathy Medical portal-systemic encephalopathy
    n. Encephalopathy associated with cirrhosis of the liver, attributed to the passage of toxic nitrogenous substances from the portal to the systemic circulation. Also called hepatic encephalopathy Wikipedia Hepatic encephalopathy Hepatic encephalopathy is a condition (usually caused by liver cirrhosis and its resultant portal hypertension ) where brain cells are damaged by a build-up of toxic substances in the blood. Signs can include impaired cognition , a flapping tremor ( asterixis ), and a decreased level of consciousness.
    Pathogenesis
    Cirrhosis (as seen in chronic alcoholism or chronic hepatitis ) will obstruct the passage of blood through the liver causing portal hypertension . This means it is difficult for blood from the intestines to go through the liver, to get back to the heart . Portal-systemic anastamoses develop, and portal blood (from the intestinal veins), will by-pass the liver, and return to the heart via another route.

    36. LU:research - Lund University Institutional Archive
    5HT and 5-HIAA in chronic experimental portal-systemic encephalopathy. brain serotonin release in experimental portal-systemic encephalopathy.
    http://lu-research.lub.lu.se/php/gateway.php?who=lr&method=getfile&file=archive/

    37. NIMULID TABLET
    Prevention and treatment of portalsystemic encephalopathy . Adults 30 to 45ml,3 or 4 times daily. Adjust dosage everyday or two to produce 2 or 3 soft
    http://www.panacea-biotec.com/products/livoluk.htm
    For the use of a Registered Medical Practitioner or a Hospital or a Laboratory only LIVOLUK Description Pharmacology Pharmacokinetics Indications ... Dosage and Administration
    Description:
    Livoluk solution is a brand of Lactulose, a synthetic disaccharide, which is highly useful in the management of portal systemic encephalopathy and also constipation. LIVOLUK is colourless to amber, syrupy liquid. Each 15ml contains:
    Lactulose 10g (As Lactulose Concentration USP) Pharmacology: TOP Pharmacokinetics: Lactulose is poorly absorbed. When given orally, only small amounts reach the blood. Urinary excretion is less than or equal to 3% and is essen­tially complete within 24 hours. Lactulose exerts its effect only in the colon. Transit time through the colon may be slow, therefore, 24-48 hours may be required to produce a normal bowel movement. Indications: Livoluk is indicated in the treatment of constipation, chronic constipation, after haemorrhoidectomy, in elderly after barium meal examination, in bed ridden or institutionalized patients and others, in prevention and treatment of portal systemic encephalopathy including the stages of hepatic pre-coma and coma. Livoluk reduces blood ammonia levels by 25% to 50%. This generally parallels improved mental state and EEG patterns. Contraindications: Livoluk is contraindicated in patients who require a low galactose diet.

    38. Welcome To Raley's And Bel Air
    called portalsystemic encephalopathy (PSE), which may lead to coma. in chronicportal-systemic encephalopathy a randomized controlled trial.
    http://www.raleys.com/cfapps/healthnotesra/healthnotes.cfm?org=raleys&ContentID=

    39. Directory Of Open Access Journals
    In twentynine patients with portal-systemic encephalopathy, grade I accountedfor 89.7% esophageal varices, 86.2% paragastric varices; grade II accounted
    http://www.doaj.org/abstract?id=90386&toc=y

    40. MotherNature.com - Liver Cirrhosis
    significantly improved portalsystemic encephalopathy (PSE).36 A second in chronic portal-systemic encephalopathy a randomized controlled trial.
    http://www.mothernature.com/Library/Ency/Index.cfm/Id/1231004
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    Cirrhosis is a condition of severe damage to the liver that impairs its ability to function normally. In the United States, the most common cause of liver cirrhosis is chronic alcoholism . Liver cirrhosis may also result from chronic viral infection of the liver ( hepatitis types B, C, and D) and a number of inherited diseases, such as cystic fibrosis , hemochromatosis, and . If severe, liver cirrhosis may lead to liver failure and death. In the Western world, liver cirrhosis is the third leading cause of death in people aged 45 to 65 (after cardiovascular disease and cancer Liver cirrhosis may also cause a dangerous brain abnormality called portal-systemic encephalopathy (PSE), which may lead to coma. Another form of cirrhosis, primary biliary cirrhosis (PBC), damages the bile ducts connecting the liver and gallbladder, and occurs primarily in women over 35 years of age. The cause of PBC is not known.

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