Guidelines for the Investigation of Chronic Diarrhoea in Adults
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Evaluation of Abnormal Liver Chemistries
ACG Clinical Guideline: Evaluation of Abnormal Liver Chemistries Paul Y. Kwo, MD, FACG, FAASLD1, Stanley M. Cohen, MD, FACG, FAASLD2, and Joseph K. Lim, MD, FACG, FAASLD3 1Division of Gastroenterology/Hepatology, Department of Medicine, Stanford University School of Medicine, Palo Alto, California, USA; 2Digestive Health Institute, University Hospitals Cleveland Medical Center and Division of Gastroenterology and Liver Disease, Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA; 3Yale Viral Hepatitis Program, Yale University School of Medicine, New Haven, Connecticut, USA. Am J Gastroenterol 2017; 112:18–35; doi:10.1038/ajg.2016.517; published online 20 December 2016 Abstract Clinicians are required to assess abnormal liver chemistries on a daily basis. The most common liver chemistries ordered are serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase and bilirubin. These tests should be termed liver chemistries or liver tests. Hepatocellular injury is defined as disproportionate elevation of AST and ALT levels compared with alkaline phosphatase levels. Cholestatic injury is defined as disproportionate elevation of alkaline phosphatase level as compared with AST and ALT levels. The majority of bilirubin circulates as unconjugated bilirubin and an elevated conjugated bilirubin implies hepatocellular disease or cholestasis. Multiple studies have demonstrated that the presence of an elevated ALT has been associated with increased liver-related mortality. A true healthy normal ALT level ranges from 29 to 33 IU/l for males, 19 to 25 IU/l for females and levels above this should be assessed. The degree of elevation of ALT and or AST in the clinical setting helps guide the evaluation. -
Endocrine Tumors of the Pancreas
Friday, November 4, 2005 8:30 - 10:30 a. m. Pancreatic Tumors, Session 2 Chairman: R. Jensen, Bethesda, MD, USA 9:00 - 9:30 a. m. Working Group Session Pathology and Genetics Group leaders: J.–Y. Scoazec, Lyon, France Questions to be answered: 12 Medicine and Clinical Pathology Group leader: K. Öberg, Uppsala, Sweden Questions to be answered: 17 Surgery Group leader: B. Niederle, Vienna, Austria Questions to be answered: 11 Imaging Group leaders: S. Pauwels, Brussels, Belgium; D.J. Kwekkeboom, Rotterdam, The Netherlands Questions to be answered: 4 Color Codes Pathology and Genetics Medicine and Clinical Pathology Surgery Imaging ENETS Guidelines Neuroendocrinology 2004;80:394–424 Endocrine Tumors of the Pancreas - gastrinoma Epidemiology The incidence of clinically detected tumours has been reported to be 4-12 per million inhabitants, which is much lower than what is reported from autopsy series (about 1%) (5,13). Clinicopathological staging (12, 14, 15) Well-differentiated tumours are the large majority of which the two largest fractions are insulinomas (about 40% of cases) and non-functioning tumours (30-35%). When confined to the pancreas, non-angioinvasive, <2 cm in size, with <2 mitoses per 10 high power field (HPF) and <2% Ki-67 proliferation index are classified as of benign behaviour (WHO group 1) and, with the notable exception of insulinomas, are non-functioning. Tumours confined to the pancreas but > 2 cm in size, with angioinvasion and /or perineural space invasion, or >2mitoses >2cm in size, >2 mitoses per 20 HPF or >2% Ki-67 proliferation index, either non-functioning or functioning (gastrinoma, insulinoma, glucagonoma, somastatinoma or with ectopic syndromes, such as Cushing’s syndrome (ectopic ACTH syndrome), hypercaliemia (PTHrpoma) or acromegaly (GHRHoma)) still belong to the (WHO group 1) but are classified as tumours with uncertain behaviour. -
Inside the Minds: the Art and Science of Gastroenterology
Gastroenterology_ptr.qxd 8/24/07 11:29 AM Page 1 Inside the Minds ™ Inside the Minds ™ The Secrets to Success in The Art and Science of Gastroenterology Gastroenterology The Art and Science of Gastroenterology is an authoritative, insider’s perspective on the var- ious challenges in this field of medicine and the key qualities necessary to become a successful Top Doctors on Diagnosing practitioner. Featuring some of the nation’s leading gastroenterologists, this book provides a Gastroenterological Conditions, Educating candid look at the field of gastroenterology—academic, surgical, and clinical—and a glimpse Patients, and Conducting Clinical Research into the future of a dynamic practice that requires a deep understanding of pathophysiology and a desire for lifelong learning. As they reveal the secrets to educating and advocating for their patients when diagnosing their conditions, these authorities offer practical and adaptable strategies for excellence. From the importance of soliciting a thorough medical history to the need for empathy towards patients whose medical problems are not outwardly visible, these doctors articulate the finer points of a profession focused on treating disorders that dis- rupt a patient’s lifestyle. The different niches represented and the breadth of perspectives presented enable readers to get inside some of the great innovative minds of today, as experts offer up their thoughts around the keys to mastering this fine craft—in which both sensitiv- ity and strong scientific knowledge are required. ABOUT INSIDETHE MINDS: Inside the Minds provides readers with proven business intelligence from C-Level executives (Chairman, CEO, CFO, CMO, Partner) from the world’s most respected companies nationwide, rather than third-party accounts from unknown authors and analysts. -
Nutrition Considerations in the Cirrhotic Patient
NUTRITION ISSUES IN GASTROENTEROLOGY, SERIES #204 NUTRITION ISSUES IN GASTROENTEROLOGY, SERIES #204 Carol Rees Parrish, MS, RDN, Series Editor Nutrition Considerations in the Cirrhotic Patient Eric B. Martin Matthew J. Stotts Malnutrition is commonly seen in individuals with advanced liver disease, often resulting from a combination of factors including poor oral intake, altered absorption, and reduced hepatic glycogen reserves predisposing to a catabolic state. The consequences of malnutrition can be far reaching, leading to a loss of skeletal muscle mass and strength, a variety of micronutrient deficiencies, and poor clinical outcomes. This review seeks to succinctly describe malnutrition in the cirrhosis population and provide clarity and evidence-based solutions to aid the bedside clinician. Emphasis is placed on screening and identification of malnutrition, recognizing and treating barriers to adequate food intake, and defining macronutrient targets. INTRODUCTION The Problem ndividuals with cirrhosis are at high risk of patients to a variety of macro- and micronutrient malnutrition for a multitude of reasons. Cirrhotic deficiencies as a consequence of poor intake and Ilivers lack adequate glycogen reserves, therefore altered absorption. these individuals rely on muscle breakdown as an As liver disease progresses, its complications energy source during overnight periods of fasting.1 further increase the risk for malnutrition. Large Well-meaning providers often recommend a variety volume ascites can lead to early satiety and decreased of dietary restrictions—including limitations on oral intake. Encephalopathy also contributes to fluid, salt, and total calories—that are often layered decreased oral intake and may lead to inappropriate onto pre-existing dietary restrictions for those recommendations for protein restriction. -
American Cancer Society Flufobt Program Implementation Guide for Primary Care Practices
Health Care Solutions From the American Cancer Society American Cancer Society FluFOBT Program Implementation Guide for Primary Care Practices EIGHTY BY 2018 Reaching 80% screened for colorectal cancer by 2018 Table of Contents Introduction ................................................................................................................................. 2 Background Information and Education .................................................................................... 3 Why Have a FluFOBT Program? .................................................................................................. 4 Colorectal Cancer Screening Eligibility ...................................................................................... 5 Colorectal Cancer Screening Recommendations ....................................................................... 6 Patient Education ......................................................................................................................... 8 How to Set Up Your FluFOBT Program .................................................................................... 10 Staff Training for Your FluFOBT Program ................................................................................ 16 Summary ..................................................................................................................................... 19 Appendix A: FluFOBT Components and Logic Model ............................................................ 20 Appendix B: Colorectal Cancer Screening Recommendations -
(NCCN Guidelines®) Colorectal Cancer Screening
NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Colorectal Cancer Screening Version 2.2017 — November 14, 2017 NCCN.org Continue Version 2.2017, 11/14/17 © National Comprehensive Cancer Network, Inc. 2017, All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN® NCCN Guidelines Version 2.2017 Panel Members NCCN Guidelines Index Table of Contents Colorectal Cancer Screening Discussion * Dawn Provenzale, MD, MS/Chair ¤ Þ Michael J. Hall, MD, MS † ∆ Robert J. Mayer, MD † Þ Duke Cancer Institute Fox Chase Cancer Center Dana-Farber/Brigham and Women’s Cancer Center * Samir Gupta, MD/Vice-chair ¤ Amy L. Halverson, MD ¶ UC San Diego Moores Cancer Center Robert H. Lurie Comprehensive Cancer Reid M. Ness, MD, MPH ¤ Center of Northwestern University Vanderbilt-Ingram Cancer Center Dennis J. Ahnen, MD ¤ University of Colorado Cancer Center Stanley R. Hamilton, MD ≠ Scott E. Regenbogen, MD ¶ The University of Texas University of Michigan Travis Bray, PhD ¥ MD Anderson Cancer Center Comprehensive Cancer Center Hereditary Colon Cancer Foundation Heather Hampel, MS, CGC ∆ Niloy Jewel Samadder, MD ¤ Daniel C. Chung, MD ¤ ∆ The Ohio State University Comprehensive Huntsman Cancer Institute at the Massachusetts General Hospital Cancer Center - James Cancer Hospital University of Utah Cancer Center and Solove Research Institute Moshe Shike, MD ¤ Þ Gregory Cooper, MD ¤ Jason B. Klapman, MD ¤ Memorial Sloan Kettering Cancer Center Case Comprehensive Cancer Center/ Moffitt Cancer Center University Hospitals Seidman Cancer Thomas P. Slavin Jr, MD ∆ Center and Cleveland Clinic Taussig David W. Larson, MD, MBA¶ City of Hope Comprehensive Cancer Institute Mayo Clinic Cancer Center Cancer Center Dayna S. -
Zollinger-Ellison Syndrome. Case Report
https://doi.org/10.15446/cr.v5n1.71686 ZOLLINGER-ELLISON SYNDROME. CASE REPORT Keywords: Gastrinoma; Zollinger-Ellison Sydrome; Multiple Endocrine Neoplasia Type 1. Palabras clave: Gastrinoma; Síndrome de Zollinger-Ellison; Neoplasia endocrina múltiple tipo 1. Juan Felipe Rivillas-Reyes Juan Leonel Castro-Avendaño Universidad Nacional de Colombia - Sede Bogotá - Facultad de Medicina - Programa de Medicina - Bogotá D.C. - Colombia. Héctor Fabián Martínez-Muñoz Universidad Nacional de Colombia - Sede Bogotá - Facultad de Medicina - Departamento de Cirugía - Bogotá D.C. - Colombia. Corresponding author Juan Felipe Rivillas-Reyes. Facultad de Medicina, Universidad Nacional de Colombia. Bogotá D.C. Colombia. Email: [email protected]. Received: 13/04/2018 Accepted: 20/11/2018 zollinger-ellison syndrome ABSTRACT RESUMEN 29 Introduction: The Zollinger-Ellison syndrome Introducción. El síndrome de Zollinger-Elli- (ZES) is a pathology caused by a neuroendo- son (SZE) es una patología producida por un crine tumor, usually located in the pancreas tumor neuroendocrino habitualmente localiza- or the duodenum, which is characterized by do a nivel duodenal o pancreático, el cual pro- elevated levels of gastrin, resulting in an ex- duce niveles elevados de gastrina, derivando cessive production of gastric acid. en hipersecreción de ácido gástrico. Case presentation: A 42-year-old female Presentación del caso. Paciente femenino patient with a history of longstanding peptic de 42 años con antecedente de enfermedad ulcer disease, who consulted due to persistent ulceropéptica de larga data, quién consulta por epigastric pain, melena and signs of peritoneal epigastralgia persistente y deposiciones meléni- irritation. Perforated peptic ulcer was suspect- cas y presenta signos de irritación peritoneal. Se ed, requiring emergency surgical intervention. -
High Quality Fecal Occult Blood Testing (FOBT) for CRC Screening: Evidence and Recommendations
High Quality Fecal Occult Blood Testing (FOBT) for CRC Screening: Evidence and Recommendations Rationale for use of FOBT High sensitivity fecal occult blood testing (FOBT) is one of the colorectal cancer screening methods recommended in guidelines from the American Cancer Society, the US Preventive Services Taskforce, and every other major medical organization. In spite of this widespread endorsement, primary care clinicians often express conviction that colonoscopy is the “gold standard” test for colorectal cancer screening and that the use of FOBT represents sub-standard care. These beliefs persist in spite of well-documented shortcomings of endoscopy (missed adenomas and cancers, higher complication rates and higher one-time costs than other screening methodologies), and the fact that access to endoscopy is limited or non- existent for a significant proportion of the U.S. population. Many clinicians are also unaware that randomized controlled trials of FOBT screening have demonstrated decreases in colorectal cancer incidence and mortality, and modeling studies suggest that the years of life saved through a high quality FOBT screening program are essentially the same as with a high quality colonoscopy based screening programs. Recent advances in stool blood screening include the emergence of new tests and improved understanding of the impact of quality factors on testing outcomes. This document provides state-of-the-science information about high quality stool testing. Types of Fecal Occult Blood Tests Two main types of FOBT are available – guaiac and immunochemical. Both types of FOBT have been shown to have reasonably high detection rates for colon and rectal cancers; adenoma detection rates are appreciably lower. -
Colorectal Cancer Screening
| PATIENT RESOURCE | Colorectal Cancer Screening You have choices when it comes to colorectal cancer screening The best test is the one that gets done * Colonoscopy Multi-target Stool DNA Test* FIT/FOBT (visual exam) (Cologuard®) (fecal immunochemical test/ fecal occult blood test) Uses a scope to look for and Finds abnormal DNA and Detects blood in How does it work? remove abnormal growths blood in the stool sample the stool sample in the colon/rectum Who is it for? Adults starting at age 45 Adults starting at age 45 Adults starting at age 45 How often? Every 10 years† Every 3 years Once a year Moderately invasive, done at Yes, done at home Yes, done at home Non-invasive? hospital or doctor office Yes, however preps have greatly No No/Yes‡ Prep required? improved in recent years Prep: night before Time to collect and mail sample Time to collect and mail sample Time it takes? Procedure: next day Covered?§ Covered by most insurers Covered by most insurers Covered by most insurers Abnormal growths (polyps) If positive, a follow-up If positive, a follow-up removed during colonoscopy Next steps colonoscopy is needed colonoscopy is needed » for evaluation *All positive results on non-colonoscopy screening tests should be followed up with a timely colonoscopy. †For adults at high risk, testing may be more frequent and should be discussed with your health care provider. ‡FIT does not require changes to diet or medication. FOBT requires changes to diet or medication. §Insurance coverage can vary; only your insurer can confirm how colon cancer screening would be covered under your insurance policy. -
Diarrhea Gastroenterology
Diarrhea Referral Guide: Gastroenterology Page 1 of 2 Diagnosis/Definition: The rectal passage of an increased number of stools per day which are watery, bloody or loosely formed. By history and stool sample. Initial Diagnosis and Management: Most patients don’t need to be worked up for their diarrhea. Most cases of diarrhea are self-limiting, caused by a gastroenteritis viral agent. Patients need to be advised to drink plenty of fluids, take some NSAIDSs or Tylenol for fevers and flu-related myalgias. If the patient comes to you with a history of bloody diarrhea, fever, severe abdominal pain, and diarrhea longer than 2 weeks or associated with electrolyte abnormalities or is elderly or immunocompromised, they need to be seen by GI. Work-up in these patients should consist of a thorough history (be sure to get travel history, medications including herbal remedies and possible infectious contacts) and physical examination. Labs should include a chem. 7, CBC with differential and stool WBCs, cultures, qualitative fecal fat. If there is the possibility that this could be antibiotic related C. difficile then order a C. diff toxin on the stool. Only order an O and P on the stool\l if the patient gives you a recent history of international travel, wildern4ess camping/hiking or may be immunocompromised. Make sure to ask about mil product ingestion as it relates to the diarrhea. Fifty percent of adult Caucasians and up to 90% of African Americans, Hispanics, and Asians have some degree of milk intolerance. If from your history and laboratory studies indicate a specific etiology the following chart may help with initial therapy. -
Colorectal Cancer Tests Save Lives: the Best Test Is the Test That Gets Done
November 2013 Colorectal Cancer Tests Save Lives The best test is the test that gets done Colorectal cancer (CRC) is the second leading cancer killer of men and women in the US, following lung cancer. The US Preventive Services Task Force (USPSTF) recommends three CRC screening tests that are effective 90% at saving lives: colonoscopy, stool tests (guaiac fecal occult About 90% of people live 5 or more blood test-FOBT or fecal immunochemical test-FIT), and years when their colorectal cancer sigmoidoscopy (now seldom done). is found early through testing. Testing saves lives, but only if people get tested. Studies show that people who are able to pick the test they prefer are more likely to actually get the test done. Increasing the use of all recommended colorectal cancer tests can save 1 in 3 more lives and is cost-effective. To increase testing, doctors, nurses, and health About 1 in 3 adults systems can: (23 million) between 50 and ◊ Offer all recommended test options with advice about each. 75 years old is not getting tested as recommended. ◊ Match patients with the test they are most likely to complete. ◊ Work with public health professionals to: ■ Get more adults tested by hiring and training “patient navigators,” who are staff that help people 1 in 10 learn about, get scheduled for, and get procedures done like colonoscopy. 10% of adults who got tested for colorectal cancer ■ Create ways to make it easier for people to get used an effective at-home FOBT/FIT kits in places other than a doctor’s office, stool test. -
Children's Gastroenterology, Hepatology, and Nutrition
GI_InsertCard 4/24/09 2:03 PM Page 1 CHILDREN’S GASTROENTEROLOGY, HEPATOLOGY, AND NUTRITION CONSULT AND REFERRAL GUIDELINES FOR COMMON GI PROBLEMS DIAGNOSIS/SYMPTOM SUGGESTIONS FOR POSSIBLE PRE-REFERRAL CONSIDER INITIAL WORK-UP THERAPY REFERRAL WHEN CHRONIC ABDOMINAL PAIN ICD-9 code – 789.0 • Weight and height percentiles • Treatment of constipation, If symptoms persist after Age: toddler to adolescence • Urinanalysis if present improvement of stooling • CBC with dif ESR or CRP • Acid suppression - H2 receptor pattern, trial of a lactose-free • Stool Studies: • Antagonist or proton pump diet and lack of response – guaiac • Inhibitor to acid suppression, referral – consider EIA antigen for giardia • Trial off lactose should be made. The child • Careful evaluation of stooling pattern may require endoscopy • Diary to look for possible triggers such as foods, (EGD) and/or colonoscopy. activities or stressors CHRONIC, NON-BLOODY DIARRHEA ICD-9 code – 787.91 • Weight and height percentiles • Treat any dietary abnormality If Symptoms persist, referral Age: preschool to adolescence • Stool studies: (e.g. high fructose and/or low fat) should be made. The child – guaiac • Try increased fiber in diet may require EGD and/or – consider leukocytes • Diary of dairy and other food colonoscopy. – culture intake in relation to symptoms – EIA antigen for giardia – C. difficile toxin titer – Reducing substances, pH, – Sudan stain (spot test for fecal fat) • CBC with differential, ESR or CRP • Albumin • Quantitative IgA and anti-tTG Antibody (screen for celiac) • Consider sweat test • Consider upper GI with small bowel follow through • Consider laxative abuse, especially in adolescent females BLOODY DIARRHEA (COLITIS) ICD-9 code – 556 • Stool studies: If evaluation is negative, food If symptoms persist, referral Age: infancy – guaiac protein allergy is likely.