Inflammatory Bowel Disease Irritable Bowel Syndrome
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IRRITABLE BOWEL SYNDROME by Michael Sperling MD
IRRITABLE BOWEL SYNDROME By Michael Sperling MD Irritable bowel syndrome (IBS) involves vague symptoms of abdominal pain, diarrhea, constipation, gas and bloating for which there is no understandable cause. Incredibly, IBS affects up to 20% of the population but only three- quarters of those people actually seek medical attention. It is the second most common reason for work absenteeism. Irritable bowel symptoms may also be related to other complaints such as belching, heartburn, swallowing problems, fullness after eating, nausea, frequent urination, painful menstruation and pain during intercourse. Extremely severe cases can sometimes be related to a history of traumatic abuse. Some common associations or factors: Michael Sperling, MD 1. ‘Spastic colon’ is frequently found along with irritable bowel syndrome. Spastic colon consists of painful muscle contractions which can be relieved by bulk agents or anti- spasm drugs. 2. Post-infectious IBS occurs when irritable bowel follows a gastrointestinal infection, such as the stomach flu. These recurrent symptoms can last up to two years. 3. Stress and anxiety can worsen IBS symptoms so occasionally anti-anxiety agents may be helpful. 4. Food intolerances classically worsen symptoms of irritable bowel in some people. Common “offending foods” include lactose, legumes (beans) and cruciferous vegetables like brussel sprouts, cauliflower, broccoli and cabbage. 5. Hypersensitivity of the bowel wall: Normal colon activity is not usually noticed however in “visceral hypersensitivity”, the bowel wall reacts painfully to normal activity. This condition may be helped by the use of low dose antidepressants, which can block these painful stimuli. Careful and selective testing of patients with these symptoms and the development of a long-term doctor/patient relationship is the key to diagnosing and managing these symptoms. -
Gastrointestinal (GI) Motility, Chronic Therapeutic Class Review
Gastrointestinal (GI) Motility, Chronic Therapeutic Class Review (TCR) March 7, 2019 No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, digital scanning, or via any information storage or retrieval system without the express written consent of Magellan Rx Management. All requests for permission should be mailed to: Magellan Rx Management Attention: Legal Department 6950 Columbia Gateway Drive Columbia, Maryland 21046 The materials contained herein represent the opinions of the collective authors and editors and should not be construed to be the official representation of any professional organization or group, any state Pharmacy and Therapeutics committee, any state Medicaid Agency, or any other clinical committee. This material is not intended to be relied upon as medical advice for specific medical cases and nothing contained herein should be relied upon by any patient, medical professional or layperson seeking information about a specific course of treatment for a specific medical condition. All readers of this material are responsible for independently obtaining medical advice and guidance from their own physician and/or other medical professional in regard to the best course of treatment for their specific medical condition. This publication, inclusive of all forms contained herein, is intended to be educational in nature and is intended to be used for informational purposes only. Send comments and suggestions to [email protected]. March 2019 Proprietary Information. Restricted Access – Do not disseminate or copy without approval. © 2004–2019 Magellan Rx Management. All Rights Reserved. FDA-APPROVED INDICATIONS Drug Manufacturer Indication(s) alosetron (Lotronex®)1 generic, . -
List of Covered Drugs
List of Covered Drugs Effective July 1, 2016 INTRODUCTION We are pleased to provide the 2011 Gold Coast Health Plan List of Covered Drugs as a useful reference and informational tool. The GCHP List of Covered Drugs can assist practitioners in selecting clinically appropriate and cost effective products for their patients. The information contained in the GCHP List of Covered Drugs is provided solely for the convenience of medical providers. We do not warrant or assure accuracy of such information nor is it intended to be comprehensive in nature. This List of Covered Drugs is not intended to be a substitute for the knowledge, expertise, skill and judgment of the medical provider in his or her choice of prescription drugs. All the information in this List of Covered Drugs is provided as a reference for drug therapy selection. Specific drug selection for an individual patient rests solely with the prescriber. We assume no responsibility for the actions or omissions of any medical provider based upon reliance, in whole or in part, on the information contained herein. The medical provider should consult the drug manufacturer's product literature or standard references for more detailed information. National guidelines can be found on the National Guideline Clearinghouse site at http://www.guideline.gov PREFACE The GCHP List of Covered Drugs is organized by sections. Each section is divided by therapeutic drug class primarily defined by mechanism of action. Unless exceptions are noted, generally all applicable dosage forms and strengths of the drug cited are included in the GCHP List of Covered Drugs. Generics should be considered the first line of prescribing. -
Therapeutic Class Overview Irritable Bowel Syndrome Agents
Therapeutic Class Overview Irritable Bowel Syndrome Agents Therapeutic Class Overview/Summary: This review will focus on agents used for the treatment of Irritable Bowel Syndrome (IBS).1-5 IBS is a gastrointestinal syndrome characterized primarily by non-specific chronic abdominal pain, usually described as a cramp-like sensation, and abnormal bowel habits, either constipation or diarrhea, in which there is no organic cause. Other common gastrointestinal symptoms may include gastroesophageal reflux, dysphagia, early satiety, intermittent dyspepsia and nausea. Patients may also experience a wide range of non-gastrointestinal symptoms. Some notable examples include sexual dysfunction, dysmenorrhea, dyspareunia, increased urinary frequency/urgency and fibromyalgia-like symptoms.6 IBS is defined by one of four subtypes. IBS with constipation (IBS-C) is the presence of hard or lumpy stools with ≥25% of bowel movements and loose or watery stools with <25% of bowel movements. When IBS is associated with diarrhea (IBS-D) loose or watery stools are present with ≥25% of bowel movements and hard or lumpy stools are present with <25% of bowel movements. Mixed IBS (IBS-M) is defined as the presence of hard or lumpy stools with ≥25% and loose or water stools with ≥25% of bowel movements. Final subtype, or unsubtyped, is all other cases of IBS that do not fall into the other classes. Pharmacological therapy for IBS depends on subtype.7 While several over-the-counter or off-label prescription agents are used for the treatment of IBS, there are currently only two agents approved by the Food and Drug Administration (FDA) for the treatment of IBS-C and three agents approved by the FDA for IBS-D. -
A Case Report of Fibro-Stenotic Crohn's Disease in the Middle
DOI: https://doi.org/10.22516/25007440.185 Case report A Case Report of Fibro-Stenotic Crohn’s Disease in the Middle Ileum as the Initial Manifestation Adriana Margarita Rey,1 Gustavo Reyes,1 Fernando Sierra,1 Rafael García-Duperly,2 Rocío López,3 Leidy Paola Prada.4 1 Gastroenterologist in the Gastroenterology and Abstract Hepatology Service of the Hospital Universitario Fundación Santa Fe de Bogotá in Bogotá, Colombia Crohn’s disease (CD) is an inflammatory bowel disease that can affect the entire gastrointestinal tract. The small 2 Colon and Rectum Surgeon in the Department of intestine is affected in about 50% of patients among whom the terminal ileum is the area most commonly affected. Surgery of the Hospital Universitario Fundación Intestinal stenosis is a common complication in CD and approximately 30% to 50% of patients present Santa Fe de Bogotá in Bogotá, Colombia 3 Pathologist at of the Hospital Universitario Fundación stenosis or penetrating lesions at the time of diagnosis. Because conventional endoscopic techniques do not Santa Fe de Bogotá and Professor at Universidad de allow evaluation of small bowel lesions, techniques such as enteroscopy and endoscopic video-capsule were los Andes in Bogotá, Colombia developed. Each has advantages and indications. 4 Third Year Internal Medicine Resident at the Hospital Universitario Fundación Santa Fe de Bogotá in We present the case of a patient with CD with localized fibrostenosis in the middle ileum which is not a Bogotá, Colombia frequent site for this type of lesion. Author for correspondence: Adriana Margarita Rey. Bogotá D.C. Colombia [email protected] Keywords ........................................ -
Nutritional Considerations in Inflammatory Bowel Disease
NUTRITION ISSUES IN GASTROENTEROLOGY, SERIES #5 Series Editor: Carol Rees Parrish, M.S., R.D., CNSD Nutritional Considerations in Inflammatory Bowel Disease by Kelly Anne Eiden, M.S., R.D., CNSD Nutrient alterations are commonplace in patients with inflammatory bowel disease. The etiology for these alterations is multifactorial. Nutrition assessment is the first step in successful nutrition management of any patient with gastrointestinal disease. Nutritional goals include assisting with nutrition risk, identifying macronutrient and micronutrient needs and implementing a nutrition plan to meet those needs. This article addresses many of the nutrition issues currently facing clinicians including: oral, enteral and parenteral nutrition, common vitamin/mineral deficiencies, medium chain triglycerides and nutrition as primary and supportive therapy. INTRODUCTION and supportive treatment in both Crohn’s and UC. The nflammatory bowel disease (IBD), encompassing following article will provide guidelines to help the both Crohn’s disease and ulcerative colitis (UC), is clinician determine nutritional risk, review specialized Ia chronic inflammatory intestinal disorder of nutrient needs and discuss nutrition as a treatment unknown etiology. A multitude of factors, including modality in the patient with IBD. drug-nutrient interactions, disease location, symp- toms, and dietary restrictions can lead to protein NUTRITION ASSESSMENT IN INFLAMMATORY energy malnutrition and specific nutritional deficien- BOWEL DISEASE cies. It is estimated that up to 85% of hospitalized IBD patients have protein energy malnutrition, based on Factors Affecting Nutritional Status abnormal anthropometric and biochemical parameters in the Patient with IBD (1,2). As Crohn’s disease can occur anywhere from There are many factors that alter nutrient intake in the mouth to anus (80% of cases in the terminal ileum), it patient with IBD. -
United States Patent (10) Patent No.: US 8,969,514 B2 Shailubhai (45) Date of Patent: Mar
USOO896.9514B2 (12) United States Patent (10) Patent No.: US 8,969,514 B2 Shailubhai (45) Date of Patent: Mar. 3, 2015 (54) AGONISTS OF GUANYLATECYCLASE 5,879.656 A 3, 1999 Waldman USEFUL FOR THE TREATMENT OF 36; A 6. 3: Watts tal HYPERCHOLESTEROLEMIA, 6,060,037- W - A 5, 2000 Waldmlegand et al. ATHEROSCLEROSIS, CORONARY HEART 6,235,782 B1 5/2001 NEW et al. DISEASE, GALLSTONE, OBESITY AND 7,041,786 B2 * 5/2006 Shailubhai et al. ........... 530.317 OTHER CARDOVASCULAR DISEASES 2002fOO78683 A1 6/2002 Katayama et al. 2002/O12817.6 A1 9/2002 Forssmann et al. (75) Inventor: Kunwar Shailubhai, Audubon, PA (US) 2003,2002/0143015 OO73628 A1 10/20024, 2003 ShaubhaiFryburg et al. 2005, OO16244 A1 1/2005 H 11 (73) Assignee: Synergy Pharmaceuticals, Inc., New 2005, OO32684 A1 2/2005 Syer York, NY (US) 2005/0267.197 A1 12/2005 Berlin 2006, OO86653 A1 4, 2006 St. Germain (*) Notice: Subject to any disclaimer, the term of this 299;s: A. 299; NS et al. patent is extended or adjusted under 35 2008/0137318 A1 6/2008 Rangarajetal.O U.S.C. 154(b) by 742 days. 2008. O151257 A1 6/2008 Yasuda et al. 2012/O196797 A1 8, 2012 Currie et al. (21) Appl. No.: 12/630,654 FOREIGN PATENT DOCUMENTS (22) Filed: Dec. 3, 2009 DE 19744O27 4f1999 (65) Prior Publication Data WO WO-8805306 T 1988 WO WO99,26567 A1 6, 1999 US 2010/O152118A1 Jun. 17, 2010 WO WO-0 125266 A1 4, 2001 WO WO-02062369 A2 8, 2002 Related U.S. -
Inflammatory Bowel Disease -IBD Crohn's Disease
Inflammatory Bowel Disease -IBD Both IBD (inflammatory bowel disease) and IBS (irritable bowel syndrome) are illnesses that affect the gastrointestinal system, and even though they have some similar symptoms, they are NOT the same. Here, we’ll explore more about the differences between those two conditions. IBD causes damage of the gastrointestinal tract due to a chronic inflammation or ulceration of the intestine. Inflammatory bowel diseases include Crohn’s disease and ulcerative colitis. Why did I get IBD? The exact cause of inflammatory bowel diseases is still not fully understood. According to some research, there are several factors involved including genetics, and/or a response to environmental factors. Crohn’s Disease What is Crohn’s disease? Crohn’s disease is an inflammatory issue that will affect anywhere along the gastro-intestinal tract (mouth, stomach, intestines, colon, ect.) What are the symptoms of Crohn’s disease? Symptoms vary depending on the part of the GI system affected but often include diarrhea, abdominal pain, fatigue, and/or weight loss. Laboratory finding may include deficiencies in vitamin B12, vitamin D, or deficiency in iron. Why did I get Crohn’s disease? The exact cause of Crohn’s disease is unknown but it is believed to have a hereditary and autoimmune component. Diet and stress can aggravate this condition. Diagnosis A doctor may order blood tests looking for deficiencies in vitamin B12, vitamin D, or deficiency in iron. Stool studies may also be ordered checking for inflammatory markers and to rule out other GI disorders. 1 Treatment Because Crohn’s disease can affect anywhere along the GI tract and the severity changes significantly from one case to the next treatment options will vary but often include glucocorticoids and/or immunosuppressors. -
Adult Intussusception
1 Adult Intussusception Saulius Paskauskas and Dainius Pavalkis Lithuanian University of Health Sciences Kaunas Lithuania 1. Introduction Intussusception is defined as the invagination of one segment of the gastrointestinal tract and its mesentery (intussusceptum) into the lumen of an adjacent distal segment of the gastrointestinal tract (intussuscipiens). Sliding within the bowel is propelled by intestinal peristalsis and may lead to intestinal obstruction and ischemia. Adult intussusception is a rare condition wich can occur in any site of gastrointestinal tract from stomach to rectum. It represents only about 5% of all intussusceptions (Agha, 1986) and causes 1-5% of all cases of intestinal obstructions (Begos et al., 1997; Eisen et al., 1999). Intussusception accounts for 0.003–0.02% of all hospital admissions (Weilbaecher et al., 1971). The mean age for intussusception in adults is 50 years, and and the male-to-female ratio is 1:1.3 (Rathore et. al., 2006). The child to adult ratio is more than 20:1. The condition is found in less than 1 in 1300 abdominal operations and 1 in 100 patients operated for intestinal obstruction. Intussusception in adults occurs less frequently in the colon than in the small bowel (Zubaidi et al., 2006; Wang et al., 2007). Mortality for adult intussusceptions increases from 8.7% for the benign lesions to 52.4% for the malignant variety (Azar & Berger, 1997) 2. Etiology of adult intussusception Unlike children where most cases are idiopathic, intussusception in adults has an identifiable etiology in 80- 90% of cases. The etiology of intussusception of the stomach, small bowel and the colon is quite different (Table 1). -
Celiac Disease Initially Misdiagnosed As Irritable Bowel Syndrome: Case Report
Open Access Case Report DOI: 10.7759/cureus.71 Celiac Disease Initially Misdiagnosed as Irritable Bowel Syndrome: Case Report Erwa Eltayib. Elmakki 1. Corresponding author: Erwa Eltayib. Elmakki, [email protected] Abstract Background: The increasing availability of serological testing & upper endoscopy has led to more frequent diagnosis of celiac disease & recognition that it may mimic Irritable bowel syndrome (IBS). Objective: The objective of the present case report is to describe the importance of screening those with vague abdominal symptoms (like patients with IBS) and iron deficiency anemia for celiac disease. Methods: We report the clinical course of a 30-year-old patient with vague abdominal symptoms initially misdiagnosed as having IBS; when the patient presented in our clinic, he was noted to have iron-deficiency anemia. On work-up for the cause of iron deficiency anemia, he was found to have celiac disease on basis of positive serological tests and small bowel biopsy result. After being placed on gluten-free diet, plus iron supplements, his abdominal symptoms and iron deficiency anemia totally improved. Conclusions: Our case demonstrates that routine screening for celiac disease should highly be considered for patients with iron-deficiency anemia and IBS. Categories: Internal Medicine Keywords: celiac disease, iron deficiency anemia, irritable bowel syndrome (ibs) Introduction Celiac disease or gluten sensitive enteropathy is an intolerance of dietary gluten that results in immunologically-mediated inflammatory damage to the small intestinal mucosal. The damage is characterized by inflammation, crypt hyperplasia, and villous atrophy [1]. Case Presentation A 30-year-old Saudi male teacher was referred to our clinic because he was incidentally found to be positive for HBsAg. -
Constipation
Constipation Caris Diagnostics Health Improvement Series What is constipation? Constipation means that a person has three bowel movements or fewer in a week. The stool is hard and dry. Sometimes it is painful to pass. You may feel‘draggy’and full. Some people think they should have a bowel movement every day. That is not really true. There is no‘right’number of bowel movements. Each person's body finds its own normal number of bowel movements. It depends on the food you eat, how much you exercise, and other things. At one time or another, almost everyone gets constipated. In most cases, it lasts for a short time and is not serious. When you understand what causes constipation, you can take steps to prevent it. What can I do about constipation? Changing what you 4. Allow yourself enough time to have a bowel movement. eat and drink and how much you exercise will help re- Sometimes we feel so hurried that we don't pay atten- lieve and prevent constipation. Here are some steps you tion to our body's needs. Make sure you don't ignore the can take. urge to have a bowel movement. 1. Eat more fiber. Fiber helps form soft, bulky stool. It 5. Use laxatives only if a doctor says you should. is found in many vegetables, fruits, and grains. Be sure Laxatives are medicines that will make you pass a stool. to add fiber a little at a time, so your body gets used to Most people who are mildly constipated do not need it slowly. -
Prediction of Premature Termination Codon Suppressing Compounds for Treatment of Duchenne Muscular Dystrophy Using Machine Learning
Prediction of Premature Termination Codon Suppressing Compounds for Treatment of Duchenne Muscular Dystrophy using Machine Learning Kate Wang et al. Supplemental Table S1. Drugs selected by Pharmacophore-based, ML-based and DL- based search in the FDA-approved drugs database Pharmacophore WEKA TF 1-Palmitoyl-2-oleoyl-sn-glycero-3- 5-O-phosphono-alpha-D- (phospho-rac-(1-glycerol)) ribofuranosyl diphosphate Acarbose Amikacin Acetylcarnitine Acetarsol Arbutamine Acetylcholine Adenosine Aldehydo-N-Acetyl-D- Benserazide Acyclovir Glucosamine Bisoprolol Adefovir dipivoxil Alendronic acid Brivudine Alfentanil Alginic acid Cefamandole Alitretinoin alpha-Arbutin Cefdinir Azithromycin Amikacin Cefixime Balsalazide Amiloride Cefonicid Bethanechol Arbutin Ceforanide Bicalutamide Ascorbic acid calcium salt Cefotetan Calcium glubionate Auranofin Ceftibuten Cangrelor Azacitidine Ceftolozane Capecitabine Benserazide Cerivastatin Carbamoylcholine Besifloxacin Chlortetracycline Carisoprodol beta-L-fructofuranose Cilastatin Chlorobutanol Bictegravir Citicoline Cidofovir Bismuth subgallate Cladribine Clodronic acid Bleomycin Clarithromycin Colistimethate Bortezomib Clindamycin Cyclandelate Bromotheophylline Clofarabine Dexpanthenol Calcium threonate Cromoglicic acid Edoxudine Capecitabine Demeclocycline Elbasvir Capreomycin Diaminopropanol tetraacetic acid Erdosteine Carbidopa Diazolidinylurea Ethchlorvynol Carbocisteine Dibekacin Ethinamate Carboplatin Dinoprostone Famotidine Cefotetan Dipyridamole Fidaxomicin Chlormerodrin Doripenem Flavin adenine dinucleotide