Lactose Intolerance
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Nutritional Disturbances in Crohn's Disease ANTHONY D
Postgrad Med J: first published as 10.1136/pgmj.59.697.690 on 1 November 1983. Downloaded from Postgraduate Medical Journal (November 1983) 59, 690-697 Nutritional disturbances in Crohn's disease ANTHONY D. HARRIES RICHARD V. HEATLEY* M.A., M.R.C.P. M.D., M.R.C.P. Department of Gastroenterology, University Hospital of Wales, Cardiffand *Department ofMedicine, St James's University Hospital, Leeds LS9 7TF Summary deficiency in the same patient. The most important A wide range of nutritional disturbances may be causes of malnutrition are probably reduced food found in patients with Crohn's disease. As more intake, active inflammation and enteric loss of sophisticated tests become available to measure nutrients (Dawson, 1972). vitamin and trace element deficiencies, so these are being recognized as complications ofCrohn's disease. TABLE 1. Pathogenesis of malnutrition It is important to recognize nutritional deficiencies at an early stage and initiate appropriate treatment. Reduced food intake Anorexia Otherwise many patients, experiencing what can be a Fear of eating from abdominal pain chronic and debilitating illness, may suffer unneces- Active inflammation Mechanisms unknown Protected by copyright. sarily from the consequences of deprivation of vital Enteric loss of nutrients Exudation from intestinal mucosa nutrients. Interrupted entero-hepatic circulation Malabsorption Loss of absorptive surface from disease, resection or by-pass KEY WORDS: growth disturbance, Crohn's disease, anaemia, vitamin deficiency. Stagnant loop syndrome from strictures, fistulae or surgically created blind loops Introduction Miscellaneous Rapid gastrointestinal transit Effects of medical therapy Crohn's disease is a chronic inflammatory condi- Effects of parenteral nutrition tion ofunknown aetiology that may affect any part of without trace element supplements the gastrointestinal tract from mouth to anus. -
Celiac Disease and Lactose Intolerance
Celiac Disease and Lactose Intolerance HALINA WOJCIK, MPH, RDN, CDN AHRC, NY Celiac – Definition Celiac, also known as coeliac disease, celiac sprue, gluten-sensitive enteropathy, and non-tropical sprue is a genetic, hereditary autoimmune disorder. attributed to the specific genetic markers known as HLA-DQ2 and HLA-DQ8 that are present in affected individuals. Characteristics Sensitivity to amino acids found in the prolamin fraction of wheat (gliadin), barley (hordein), and rye (secalin), commonly known as glutens. When these grains are consumed by persons with celiac disease, they trigger an immune response that results in damage to the person’s mucosa of the small intestine. This damage causes the malabsorption of macronutrients and micronutrients. Source: Nutrition Care Manual. Academy of Nutrition and Dietetics. 2019: Gastrointestinal Disease: Celiac. Available from [https://www.nutritioncaremanual.org ] Comparison of lining of the small intestine in healthy individual and person with Celiac disease Prevalence of Celiac in the United States 1% of population ~ 3 million Americans It’s about the same number of people living in the state of Nevada. In the general US population: 1 in 133 people In people with first - degree relatives (parent, child, sibling) who has celiac: 1 in 22 In people with second degree relatives (aunt, uncle, cousin) who has celiac: 1 in 39 Source: Nutrition Care Manual. Academy of Nutrition and Dietetics. 2019: Gastrointestinal Disease: Celiac. Available from [https://www.nutritioncaremanual.org ] Prevalence of Celiac Disease (CD) in Down Syndrome (DS) Ample of studies suggest that CD is higher in individuals with Down Syndrome. 1 The meta-analysis study ( 31 studies included 4383 individuals) showed that individuals with DS are at very high risk of CD. -
Does Your Patient Have Bile Acid Malabsorption?
NUTRITION ISSUES IN GASTROENTEROLOGY, SERIES #198 NUTRITION ISSUES IN GASTROENTEROLOGY, SERIES #198 Carol Rees Parrish, MS, RDN, Series Editor Does Your Patient Have Bile Acid Malabsorption? John K. DiBaise Bile acid malabsorption is a common but underrecognized cause of chronic watery diarrhea, resulting in an incorrect diagnosis in many patients and interfering and delaying proper treatment. In this review, the synthesis, enterohepatic circulation, and function of bile acids are briefly reviewed followed by a discussion of bile acid malabsorption. Diagnostic and treatment options are also provided. INTRODUCTION n 1967, diarrhea caused by bile acids was We will first describe bile acid synthesis and first recognized and described as cholerhetic enterohepatic circulation, followed by a discussion (‘promoting bile secretion by the liver’) of disorders causing bile acid malabsorption I 1 enteropathy. Despite more than 50 years since (BAM) including their diagnosis and treatment. the initial report, bile acid diarrhea remains an underrecognized and underappreciated cause of Bile Acid Synthesis chronic diarrhea. One report found that only 6% Bile acids are produced in the liver as end products of of British gastroenterologists investigate for bile cholesterol metabolism. Bile acid synthesis occurs acid malabsorption (BAM) as part of the first-line by two pathways: the classical (neutral) pathway testing in patients with chronic diarrhea, while 61% via microsomal cholesterol 7α-hydroxylase consider the diagnosis only in selected patients (CYP7A1), or the alternative (acidic) pathway via or not at all.2 As a consequence, many patients mitochondrial sterol 27-hydroxylase (CYP27A1). are diagnosed with other causes of diarrhea or The classical pathway, which is responsible for are considered to have irritable bowel syndrome 90-95% of bile acid synthesis in humans, begins (IBS) or functional diarrhea by exclusion, thereby with 7α-hydroxylation of cholesterol catalyzed interfering with and delaying proper treatment. -
Management of Food Allergies
Management of Food Allergies Federal Bureau of Prisons Clinical Practice Guidelines September 2012 Clinical guidelines are made available to the public for informational purposes only. The Federal Bureau of Prisons (BOP) does not warrant these guidelines for any other purpose, and assumes no responsibility for any injury or damage resulting from the reliance thereof. Proper medical practice necessitates that all cases are evaluated on an individual basis and that treatment decisions are patient specific. Consult the BOP Clinical Practice Guideline Web page to determine the date of the most recent update to this document: http://www.bop.gov/news/medresources.jsp. i Federal Bureau of Prisons Management of Food Allergies Clinical Practice Guidelines September 2012 Table of Contents 1. Purpose .................................................................................................................................1 2. Food Allergy Overview ........................................................................................................1 3. Food Allergy Assessment .....................................................................................................3 4. Evaluation and Management of Potential Anaphylactic Food Allergies............................4 5. Evaluation and Management of Potential Non-Anaphylactic Food Allergies ...................4 6. Diet Orders ...........................................................................................................................4 Medical Diet Orders/Self-Selection -
Malabsorption and Exocrine Pancreatic Insuffiecienty (Pi)
MALABSORPTION AND EXOCRINE PANCREATIC INSUFFIECIENTY (PI) Pancreatic Insufficiency is a condition in which a person does not have enough enzymes and bicarbonate being delivered from the pancreas to the intestine for digestion. This causes mal- absorption of nutrients, failure to gain weight and grow, weight loss, vitamin and mineral deficiency, and gastrointestinal symptoms. Most people with CF have mal-absorption due to PI. Onset usually occurs in the first one to two years of life, often in early infancy, but can start at anytime. Symptoms of mal-absorption -Change in number of stools -Large, bulky stools -Stools may be bulky and soft -Greasy, oily or floating stools, oil in toilet water -Stools may smell worse than usual or normal -Rectal prolapse -Mal-absorption of calorie providing nutrients and poor weight gain or weight loss Fat …………………………………………….9 calories/gram Protein………………………………..…….4 calories/gram Complex Carbohydrate ……………..4 calories/gram -Results in poor weight gain, weight loss, poor growth, decreased immune function and decreased lung health. -Mal-absorption of FAT SOLUBLE VITAMIN and deficiency: Vitamin A, Vitamin D, Vitamin E, Vitamin K -Mineral deficiencies: Calcium, Zinc, Sodium, Chloride Learn more about vitamins and minerals at: http://www.cff.org/treatments/Therapies/Nutrition/Vitamins/ Tests to Diagnose PI and Mal-absorption -72 hr fecal fat test -Pancreatic Fecal Elastase Treatment of PI and Mal-absorption Pancreatic Enzyme Replacement Therapy (PERT) Pancreatic enzymes are taken with each meal, snack, breast feed, bottle , and drink that contains fat protein and or complex carbohydrate. Antacid and acid blocking medicines can be added to make enzymes work better Fat Soluble Vitamin Supplementation with special supplements made for mal-absorption are prescribed Each enzyme company offers programs that provide free nutritional support and/or CF therapy support High Calorie, high protein diet Even with PERT, not all calories and nutrients from food are absorbed as expected and calories and nutrients are lost and need replacement. -
Digestive Health Center Nutrition Services Nutrition Guidelines for Chronic Pancreatitis Patient Education
Digestive Health Center Nutrition Services Nutrition Guidelines for Chronic Pancreatitis Patient Education The pancreas is an organ that: Produces pancreatic enzymes to help digest (break down) food in the small intestine for absorption Makes hormones (such as insulin) to help control blood sugars Chronic pancreatitis is ongoing inflammation of the pancreas. Symptoms can be worse after eating. Symptoms include: Abdominal pain Nausea Vomiting Weight loss Fatty stools (stools may also float and/or have a foul odor) Malabsorption of nutrients can occur from poor digestion of food (due to reduced pancreatic enzyme activity), which will result in nutrients passing into the stools. This is seen especially with fat and fat soluble vitamins (A, D, E) as digestion of fat is highly dependent on pancreatic enzymes. In some cases, diabetes can develop if the pancreas is not able to make enough insulin to help control blood sugars, so blood sugars stay high. Nutritional Guidelines Follow a low fat diet, which for chronic pancreatitis is often restricted to 50 grams of fat, but could also range between 30-50 grams of fat depending on tolerance. If you have diabetes, eat recommended serving sizes of low fat carbohydrates to help control blood sugars (low fat/non fat dairy, fruits, vegetables, whole grains, beans, lentils etc). Information on serving sizes is available. Take pancreatic enzymes as prescribed by your doctor to treat malabsorption. Take the enzymes before each meal and snack. They will not work if taken at the end of the meal. 1 Low Fat Diet Tips Eat 4-6 small meals throughout the day Spread out your fat intake throughout the day Use butter, margarine and cooking oils sparingly Bake, grill, roast and/or steam foods. -
8 LECTURES Gastro-Esophageal Reflux Disease Peptic Ulcer
8 LECTURES Gastro-esophageal reflux disease Peptic Ulcer Disease Diarrhea Malabsorption Inflammatory bowel disease-1 Inflammatory bowel disease-2 Colonic polyps and carcinoma-1 Colonic polyps and carcinoma-2 8 LECTURES Diarrhea Malabsorption DIARREAHA Objectives Upon completion of this lecture the students should : 1. Understand the physiology of fluid in small intestine 2. Describe the pathophysiology and causes of various types of diarrhea ( Secretory, osmotic, Exudative, Motility-related ) 3. Define acute diarrhea and enumerate its common causes 4. Define chronic diarrhea and enumerate its common causes Physiology of Fluid and small intestine DIARREAHA DEFINITION • World Health Organization 3 or more loose or liquid stools per day • Abnormally high fluid content of stool > 200-300 gm/day Fecal osmolarity • As stool leaves the colon, fecal osmolality is equal to the serum osmolality i.e. 290 mosm/kg. • Under normal circumstances, the major osmoles + + – – are Na , K , Cl , and HCO3 . CLASSIFICATION 1.Acute …………….if 2 weeks, 2.Persistent ……. if 2 to 4 weeks, 3.Chronic ………..if 4 weeks in duration. Why important? • The loss of fluids through diarrhea can cause dehydration and electrolyte imbalances • Easy to treat but if untreated, may lead to death especially in children Why important? More than 70 % of almost 11 million child deaths every year are attributable to 6 causes: 1. Diarrhea 2. Malaria 3. neonatal infection 4. Pneumonia 5. preterm delivery 6. lack of oxygen at birth. UNICEF Pathophysiology Categories of diarrhea 1. Secretory 2. Osmotic 3. Exudative (inflammatory ) 4. Motility-related Secretory • There is an increase in the active secretion • High stool output • Lack of response to fasting • Normal stool osmotic gap < 100 mOsm/kg • The most common cause of this type of diarrhea is a bacterial toxin ( E. -
Lactose-Intolerant Kids Should Get Some Dairy
50 Digestive Disorders FAMILY P RACTICE N EWS • October 15, 2006 Lactose-Intolerant Kids Should Get Some Dairy BY MICHELE G. SULLIVAN The document is the first AAP lactose tive Americans, followed by blacks and “The avoidance of milk products to Mid-Atlantic Bureau guideline update since 1990 (Pediatrics Hispanics. The incidence is very low in control symptoms may be problematic 2006;118:1279-86). whites, whose northern European her- for optimal bone mineralization. Children t is usually not necessary to eliminate A statement from the American Dairy itage seems to be protective, according the who avoid milk have been documented to dairy foods from the diets of lactose-in- Council hailed the AAP guidelines as a guidelines. Among white children, symp- ingest less than the recommended Itolerant children and adolescents, and common sense approach to a problem toms typically don’t develop until after age amounts of calcium needed for normal doing so may compromise their long-term that sometimes prevents children from 4 or 5 years; they may manifest earlier in bone calcium accretion and bone miner- skeletal health. getting milk’s unique nutritional package other groups. alization.” Most of these patients still can consume of protein, vitamins, and minerals. Newborns who develop intractable di- Most lactose-intolerant children can enough dairy every day to meet their cal- “Although calci- arrhea after consum- tolerate varying amounts of dairy, de- cium and vitamin D needs, especially if um-fortified bever- Rice and soy milks are not ing any mammalian pending on their individual symptoms: they drink lactose-reduced milk and eat ages and other foods milk product, includ- One glass of milk may be fine, but two yogurt with live cultures and/or aged can provide an alter- good substitutes for dairy ing human milk, may may provoke diarrhea. -
Do Patients with Lactose Intolerance Exhibit More Frequent Comorbidities
ORIGINAL ARTICLE Annals of Gastroenterology (2016) 29, 174-179 Do patients with lactose intolerance exhibit more frequent comorbidities than patients without lactose intolerance? An analysis of routine data from German medical practices Rebecca Schiff nera, Karel Kostevb, Holger Gothea,c University for Health Sciences, Medical Informatics and Technology, Hall in Tirol, Austria; IMS Health, Epidemiology, Frankfurt am Main, Germany; University of Technology Dresden, Dresden, Germany Abstract Background Th e increase in food intolerances poses a burgeoning problem in our society. Food intolerances not only lead to physical impairment of the individual patient but also result in a high socio-economic burden due to factors such as the treatment required as well as absenteeism. Th e present study aimed to explore whether lactose intolerant (LI) patients exhibit more frequent comorbidities than non-LI patients. Methods Th e study was conducted on a case-control basis and the results were determined using routine data analysis. Routine data from the IMS Disease Analyzer database were used for this purpose. A total of 6,758 data records were processed and analyzed. Results Th ere were signifi cant correlations between LI and the incidence of osteoporosis, changes in mental status, and the presence of additional food intolerances. Comparing 3,379 LI vs. 3,379 non-LI patients, 34.5% vs. 17.7% (P<0.0001) suff ered from abdominal pain; 30.6% vs. 17.2% (P<0.0001) from gastrointestinal infections; and 20.9% vs. 16.0% (P=0.0053) from depression. Adjusted odds ratios (OR) were the highest for fructose intolerance (n=229 LI vs. -
Lactose Intolerance Brochure
Lactose Intolerance Albert F. Chiemprabha, M.D. Pierce D. Dotherow, M.D. Reed B. Hogan, M.D. James H. Johnston, III, M.D. Ronald P. Kotfila, M.D. Billy W. Long, M.D. J. Trippe McNeese, M.D. Paul B. Milner, M.D. Michelle A. Petro, M.D. Vonda Reeves-Darby, M.D. Sara Rippel, M.D., Pediatric GI Matt Runnels, M.D. Vishwanath N. Shenoy, M.D. James Q. Sones, II, M.D. April Ulmer, M.D., Pediatric GI James A. Underwood, Jr., M.D. Mark E. Wilson, M.D. Cindy Haden Wright, M.D. Keith Brown, M.D., Pathologist Samuel Hensley, M.D., Pathologist Jackson Madison Vicksburg 1421 N. State Street, Ste 203 106 Highland Way 1815 Mission 66 Jackson, MS 39202 Madison, MS 39110 Vicksburg, MS 39180 601/355-1234 601/355-1234 601/638-8801 Fax 601/352-4882 • 800/880-1231 www.msgastrodocs.com ©2011 GI Associates & Endoscopy Center. All rights reserved. Dairy Products Calcium Content Lactose Content Table of contents Ice cream/ice milk (8 oz.) 176 mg. 6-7g Milk 291-316 mg. 12-13g (whole, low-fat, skim, buttermilk, 8 oz.) Processed cheese (1 oz.) 159-215 mg. 12-13g Sour cream (4 oz.) 134 mg. 4-5g Yogurt (plain, 8 oz.) 274-415 mg. 12-13g Fish/Seafood Calcium Content Lactose Content Oysters (1 cup, raw) 226 mg. 0 Salmon with bones (canned, 3 oz.) 167 mg. 0 Sardines (3 oz.) 371 mg. 0 Shrimp (canned, 3 oz.) 98 mg. 0 Other Calcium Content Lactose Content Molasses (2 tbsp.) 274 mg. -
Lactose Intolerance and Health: Evidence Report/Technology Assessment, No
Evidence Report/Technology Assessment Number 192 Lactose Intolerance and Health Prepared for: Agency for Healthcare Research and Quality U.S. Department of Health and Human Services 540 Gaither Road Rockville, MD 20850 www.ahrq.gov Contract No. HHSA 290-2007-10064-I Prepared by: Minnesota Evidence-based Practice Center, Minneapolis, MN Investigators Timothy J. Wilt, M.D., M.P.H. Aasma Shaukat, M.D., M.P.H. Tatyana Shamliyan, M.D., M.S. Brent C. Taylor, Ph.D., M.P.H. Roderick MacDonald, M.S. James Tacklind, B.S. Indulis Rutks, B.S. Sarah Jane Schwarzenberg, M.D. Robert L. Kane, M.D. Michael Levitt, M.D. AHRQ Publication No. 10-E004 February 2010 This report is based on research conducted by the Minnesota Evidence-based Practice Center (EPC) under contract to the Agency for Healthcare Research and Quality (AHRQ), Rockville, MD (Contract No. HHSA 290-2007-10064-I). The findings and conclusions in this document are those of the authors, who are responsible for its content, and do not necessarily represent the views of AHRQ. No statement in this report should be construed as an official position of AHRQ or of the U.S. Department of Health and Human Services. The information in this report is intended to help clinicians, employers, policymakers, and others make informed decisions about the provision of health care services. This report is intended as a reference and not as a substitute for clinical judgment. This report may be used, in whole or in part, as the basis for the development of clinical practice guidelines and other quality enhancement tools, or as a basis for reimbursement and coverage policies. -
Liver Cirrhosis: a Patient Resource Guide
LIVER CIRRHOSIS: A PATIENT RESOURCE GUIDE 502-588-4600 What is the liver? The liver is the body’s largest internal organ. It is an essential organ and the body cannot survive without it. The liver has many important functions including: • Preventing infections • Removing bacteria and toxins from the blood • Produce “juices” needed for digesting food and processing medications and hormones • Making proteins that help the blood clot • Storing vitamins, minerals, fats, and sugars for use by the body Normal liver liver with cirrhosis What is liver cirrhosis? When something attacks and damages the liver, liver cells are killed and scar tissue is formed. This scarring process is called fibrosis (pronounced “fi-bro-sis”), and it happens slowly over many years. When the whole liver is scarred, it shrinks and hardens. This is called cirrhosis. Any illness that affects the liver over a long period of time may lead to fibrosis and, eventually, cirrhosis. Heavy drinking and viruses (like hepatitis C or B) are common causes of cirrhosis. However, there are other causes as well. Cirrhosis may be caused by a buildup of fat in the liver of people who are overweight or have diabetes. Some people inherit genes that cause liver disease. Other causes include certain prescribed and over-the-counter medicines, environmental poisons, and autoimmune liver disease, a condition in which a person’s own immune system attacks the liver as if it were a foreign body. What happens when you have cirrhosis? Cirrhosis causes the liver to become lumpy and stiff. This prevents blood from flowing through the liver easily and causes the build-up of pressure in the portal vein, the vein that brings blood to the liver.