Management of Adult Patients with Ascites Due to Cirrhosis: Update 2012

Total Page:16

File Type:pdf, Size:1020Kb

Management of Adult Patients with Ascites Due to Cirrhosis: Update 2012 © 2012 The American Association for the Study of Liver Diseases, All rights reserved. rights All Diseases, Liver of Study the for Association American The 2012 © FORWARD REFERENCES FULL TEXT FULL RECOMMENDATIONS CONTENTS Jump to: Jump PRACTICE GUIDELINE PRACTICE Bruce A. Runyon A. Bruce Update 2012 Update with Ascites Due to Cirrhosis: Cirrhosis: to Due Ascites with Management of Adult Patients Patients Adult of Management AASLD Management of Adult Patients with Ascites PRACTICE GUIDELINE Due to Cirrhosis: Update 2012 CONTENTS RECOMMENDATIONS FULL TEXT REFERENCES WEB SITE Contents (click section title or page number) Recommendations and Rationales .......................... 3 Full-text Guideline ..................................... 56 Abbreviations ........................................ 57 Preamble ........................................... 58 Introduction ......................................... 58 Evaluation and Diagnosis ............................... 59 Ascitic Fluid Analysis ................................... 62 Differential Diagnosis ................................... 63 Treatment of Ascites ................................... 64 Refractory Ascites ..................................... 70 Spontaneous Bacterial Peritonitis .......................... 74 Prevention of SBP ..................................... 79 Hepatorenal Syndrome ................................. 81 Additional Considerations ................................ 84 Hepatic Hydrothorax ................................... 85 References .......................................... 87 USING, SEARCHING, AND PRINTING GUIDELINES This document was designed for use on a variety Use the top menu to return to the list. This file reflects of devices using Adobe Acrobat Reader.® Smaller the most recently approved language of the published screens should be held horizontally. You may search guideline. Your feedback is welcome on the design and or print using your PDF viewer. Menu hyperlinks allow usability and will help guide future publications. movement between sections and to the guidelines on Please email your comments the AASLD site. In Recommendations and Rationales, to [email protected] click on individual items to review specific rationales. or visit our social media pages. BACK 2 FORWARD © 2012 The American Association for the Study of Liver Diseases, All rights reserved. AASLD Management of Adult Patients with Ascites PRACTICE GUIDELINE Due to Cirrhosis: Update 2012 CONTENTS RECOMMENDATIONS FULL TEXT REFERENCES WEB SITE Recommendations and Rationales This guideline includes 49 specific recommendations. Please click on a recommendation to review the related ratio- nale and supporting evidence. See Table 1 for an explanation of the grading system for recommendations. 1. Diagnostic abdominal paracentesis should 9. First-line treatment of patients with be performed and ascitic fluid should be cirrhosis and ascites consists of sodium obtained from inpatients and outpatients restriction (88 mmol per day [2000 mg with clinically apparent new-onset ascites. per day], diet education,) and diuretics (Class I, Level C) (oral spironolactone with or without oral furosemide). (Class IIa, Level A) 2. Since bleeding is sufficiently uncommon, the routine prophylactic use of fresh frozen 10. Fluid restriction is not necessary unless plasma or platelets before paracentesis is serum sodium is less than 125 mmol/L. not recommended. (Class III, Level C) (Class III, Level C) 3. The initial laboratory investigation of ascitic 11. Vaptans may improve serum sodium in fluid should include an ascitic fluid cell patients with cirrhosis and ascites. However count and differential, ascitic fluid total their use does not currently appear justified protein, and serum-ascites albumin gradient. in view of their expense, potential risks, (Class I, Level B) and lack of evidence of efficacy in clinically meaningful outcomes. (Class III, Level A) 4. If ascitic fluid infection is suspected, ascitic fluid should be cultured at the bedside in 12. An initial therapeutic abdominal paracentesis aerobic and anaerobic blood culture bottles should be performed in patients with tense prior to initiation of antibiotics. (Class I, Level B) ascites. Sodium restriction and oral diuretics should then be initiated. (Class IIa, Level C) 5. Other studies of ascitic fluid can be ordered based on the pretest probability of disease 13. Diuretic-sensitive patients should preferably (Table 3). (Class IIa, Level C) be treated with sodium restriction and oral diuretics rather than with serial 6. Testing serum for CA125 is not helpful in the paracenteses. (Class IIa, Level C) differential diagnosis of ascites. Its use is not recommended in patients with ascites of 14. Use of angiotensin converting enzyme any type. (Class III, Level B) inhibitors and angiotensin receptor blockers in patients with cirrhosis and ascites may 7. Patients with ascites who are thought be harmful, must be carefully considered in to have an alcohol component to their each patient, monitoring blood pressure and liver injury should abstain from alcohol renal function. (Class III, Level C) consumption. (Class I, Level B) 15. The use of nonsteroidal anti-inflammatory 8. Baclofen can be given to reduce alcohol drugs should be avoided in patients with craving and alcohol consumption in patients cirrhosis and ascites, except in special with ascites in the setting of alcoholic liver circumstances. (Class III, Level C) disease. (Class IIb, Level C) BACK 3 FORWARD © 2012 The American Association for the Study of Liver Diseases, All rights reserved. AASLD Management of Adult Patients with Ascites PRACTICE GUIDELINE Due to Cirrhosis: Update 2012 CONTENTS RECOMMENDATIONS FULL TEXT REFERENCES WEB SITE 16. Liver transplantation should be considered 25. Peritoneovenous shunt, performed by in patients with cirrhosis and ascites. a surgeon or inteventional radiologist (Class I, Level B) experienced with this technique, should be considered for patients with refractory 17. The risks versus benefits of beta blockers ascites who are not candidates for must be carefully weighed in each paracenteses, transplant, or TIPS. patient with refractory ascites. Systemic (Class IIb, Level A) hypotension often complicates their use. Consideration should be given to 26. Patients with ascites admitted to the hospital discontinuing or not initiating these drugs in should undergo abdominal paracentesis. this setting. (Class III, Level B) Paracentesis should be repeated in patients (whether in the hospital or not) who 18. The use of angiotensin converting enzyme develop signs or symptoms or laboratory inhibitors and angiotensin receptor blockers abnormalities suggestive of infection should be avoided in patients refractory (e.g., abdominal pain or tenderness, fever, ascites. Systemic hypotension often encephalopathy, renal failure, acidosis, or complicates their use. (Class III, Level B) peripheral leukocytosis). (Class I, Level B) 19. Oral midodrine has been shown to improve 27. Patients with ascitic fluid polymorphonuclear clinical outcomes and survival in patients leukocyte counts greater than or equal with refractory ascites; its use should be to 250 cells/mm3 (0.25 x 109/L) in a considered in this setting. (Class IIa, Level B) community-acquired setting in the absence 20. Serial therapeutic paracenteses are a of recent Β-lactam antibiotic exposure treatment option for patients with refractory should receive empiric antibiotic therapy, ascites. (Class I, Level C) e.g., an intravenous third-generation cephalosporin, preferably cefotaxime 2 g 21. Post-paracentesis albumin infusion may not every 8 hours. (Class I, Level A) be necessary for a single paracentesis of less than 4 to 5 L. (Class I, Level C) 28. Patients with ascitic fluid polymorphonuclear leukocyte counts greater than or equal 22. For large-volume paracenteses, an to 250 cells/mm3 (0.25 x 109/L) in a albumin infusion of 6-8 g per liter of fluid nosocomial setting and/or in the presence removed appears to improve survival and is of recent Β-lactam antibiotic exposure recommended. (Class IIa, Level A) should receive empiric antibiotic therapy based on local susceptibility testing of 23. Referral for liver transplantation should be bacteria in patients with cirrhosis. expedited in patients with refractory ascites, (Class IIa, Level B) if the patient is otherwise a candidate for transplantion. (Class IIa, Level C) 29. Oral ofloxacin (400 mg twice per day) can be considered a substitute for intravenous 24. Transjugular intrahepatic portosystemic cefotaxime in inpatients without prior stent-shunt (TIPS) may be considered exposure to quinolones, vomiting, shock, in appropriately selected patients who grade II (or higher) hepatic encephalopathy, meet criteria similar to those of published or serum creatinine greater than 3 mg/dL. randomized trials. (Class I, Level A) (Class IIa, Level B) BACK 4 FORWARD © 2012 The American Association for the Study of Liver Diseases, All rights reserved. AASLD Management of Adult Patients with Ascites PRACTICE GUIDELINE Due to Cirrhosis: Update 2012 CONTENTS RECOMMENDATIONS FULL TEXT REFERENCES WEB SITE 30. Patients with ascitic fluid polymorphonuclear 34. Intravenous ceftriaxone for 7 days or leukocyte counts less than 250 cells/mm3 twicedaily norfloxacin for 7 days should (0.25 x 109/L) and signs or symptoms of be given to prevent bacterial infections in infection (temperature >100° F or abdominal patients with cirrhosis and gastrointestinal pain or tenderness) should also receive
Recommended publications
  • Laparoscopy As a Diagnostic Tool in Ascites of Unknown Origin: a Retrospective Study Conducted at Kasturba Hospital, Manipal
    Research Article Open Access J Surg Volume 8 Issue 3 - March 2018 Copyright © All rights are reserved by Chetan R Kulkarni DOI: 10.19080/OAJS.2018.08.555740 Laparoscopy as a Diagnostic Tool in Ascites of Unknown Origin: A Retrospective Study Conducted at Kasturba Hospital, Manipal Chetan R Kulkarni1*, Badareesh Laxminarayan2 and Annappa Kudva3 1Assistant Professor, Department of Surgery, Kasturba Hospital, Manipal 2Associate Professor, Department of Surgery, Kasturba Hospital, Manipal 3Professor, Department of Surgery, Kasturba Hospital, Manipal Received: February 16, 2018; Published: March 01, 2018 *Corresponding author: Chetan R Kulkarni, Assistant Professor, Department of Surgery, Kasturba Hospital, Manipal, India. Tel: 9535974395;Email: Abstract Background: Laparoscopy as a minimally invasive technique has long played an important role in the evaluation of ascites. Methods: A retrospective analysis was carried out on the record of 80patients who underwent laparoscopy after appropriate investigations had failed to reveal the cause of ascites. Results: Tuberculous peritonitis was reported in 46(57%), malignancies in 18(25%), cirrhosis in 4(5%) and peritonitis of unknown etiology in 8(10%)Conclusion: of patients. Two (2.5%) patients had complications, an Ileal perforation and in other Incisional hernia. Keywords: Ascites;Laparoscopy Diagnostic was Laparoscopy able to diagnose the pathology in 72 (90%) patients with ascites of unknown origin. Introduction Laparoscopy, as a minimally invasive technique has developed rapidly in recent years. Endoscopic examination of conventional laboratory examinations (including ascitic fluid cell count, albumin level, total protein level, Gram stain, culture who termed it as “Celioscopy” [1,2]. The term ‘ascites’ refers to and cytology ) as well as after imaging investigations (including peritoneal cavity was first attempted in 1901 by George Kelling Materialultrasound andand CT Methods scan).
    [Show full text]
  • 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.
    [Show full text]
  • Recurrent Pneumothorax Following Abdominal Paracentesis
    Postgrad Med J (1990) 66, 319 - 320 © The Fellowship of Postgraduate Medicine, 1990 Postgrad Med J: first published as 10.1136/pgmj.66.774.319 on 1 April 1990. Downloaded from Recurrent pneumothorax following abdominal paracentesis P.J. Stafford Department ofMedicine, Newham General Hospital, Glen Road, Plaistow, London E13, UK. Summary: A 62 year old man presented with abdominal ascites, without pleural effusion, due to peritoneal mesothelioma. He had chronic obstructive airways disease and a past history of right upper lobectomy for tuberculosis. On two occasions abdominal paracentesis was followed within 72 hours by pneumothorax. This previously unreported complication of abdominal paracentesis may be due to increased diaphragmatic excursion following the procedure and should be considered in patients with preexisting lung disease. Introduction Abdominal paracentesis is a widely used palliative right iliac fossa. Approximately 4 litres of turbid therapy for malignant ascites and is generally fluid was drained over 72 hours. The protein accepted as a procedure with few adverse effects: concentration was 46 g/l and microbiology and pneumothorax is not a recognized complication. I cytology were not diagnostic. Laparoscopy re- report a patient with recurrent pneumothorax vealed matted loops of bowel with widespread apparently precipitated by abdominal paracen- peritoneal seedlings. Histological examination of copyright. tesis. these lesions showed malignant mesothelioma of the epithelioid type. The patient suffered a left pneumothorax within Case report 48 hours ofparacentesis (before laparoscopy). This was treated with intercostal underwater drainage A 62 year old civil servant presented with a 6-week but recurred on two attempts to remove the drain, history ofworsening abdominal distension.
    [Show full text]
  • 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.
    [Show full text]
  • Acute Liver Failure J G O’Grady
    148 Postgrad Med J: first published as 10.1136/pgmj.2004.026005 on 4 March 2005. Downloaded from REVIEW Acute liver failure J G O’Grady ............................................................................................................................... Postgrad Med J 2005;81:148–154. doi: 10.1136/pgmj.2004.026005 Acute liver failure is a complex multisystemic illness that account for most cases, but a significant number of patients have no definable cause and are evolves quickly after a catastrophic insult to the liver classified as seronegative or of being of indeter- leading to the development of encephalopathy. The minate aetiology. Paracetamol is the commonest underlying aetiology and the pace of progression strongly cause in the UK and USA.2 Idiosyncratic reac- tions comprise another important group. influence the clinical course. The commonest causes are paracetamol, idiosyncratic drug reactions, hepatitis B, and Viral seronegative hepatitis. The optimal care is multidisciplinary ALF is an uncommon complication of viral and up to half of the cases receive liver transplants, with hepatitis, occurring in 0.2%–4% of cases depend- ing on the underlying aetiology.3 The risk is survival rates around 75%–90%. Artificial liver support lowest with hepatitis A, but it increases with the devices remain unproven in efficacy in acute liver failure. age at time of exposure. Hepatitis B can be associated with ALF through a number of ........................................................................... scenarios (table 2). The commonest are de novo infection and spontaneous surges in viral repli- cation, while the incidence of the delta virus cute liver failure (ALF) is a complex infection seems to be decreasing rapidly. multisystemic illness that evolves after a Vaccination should reduce the incidence of Acatastrophic insult to the liver manifesting hepatitis A and B, while antiviral drugs should in the development of a coagulopathy and ameliorate replication of hepatitis B.
    [Show full text]
  • Atypical Abdominal Pain in a Patient with Liver Cirrhosis
    IMAGE IN HEPATOLOGY January-February, Vol. 17 No. 1, 2018: 162-164 The Official Journal of the Mexican Association of Hepatology, the Latin-American Association for Study of the Liver and the Canadian Association for the Study of the Liver Atypical Abdominal Pain in a Patient With Liver Cirrhosis Liz Toapanta-Yanchapaxi,* Eid-Lidt Guering,** Ignacio García-Juárez* * Gastroenterology Department. National Institute of Medical Science and Nutrition “Salvador Zubirán”. Mexico City. Mexico. ** Interventional Cardiology. National Institute of Cardiology “Ignacio Chávez”. Mexico City. Mexico. ABSTRACTABSTABSTABSTRACT The causes of abdominal pain in patients with liver cirrhosis and ascites are well-known but occasionally, atypical causes arise. We report the case of a patient with a ruptured, confined abdominal aortic aneurysm. KeyK words.o d .K .Key Liver cirrhosis. Abdominal aortic aneurysm. INTRODUCTION CASE REPORT Abdominal pain in cirrhotic patients is a challenge. A 47-year-old male with the established diagnosis of Clinical presentation can be non-specific and the need for alcohol-related liver cirrhosis, presented to the emer- early surgical exploration may be difficult to assess. Coag- gency department for abdominal pain. He was classified ulopathy, thrombocytopenia, varices, and ascites need to as Child Pugh (CP) C stage (10 points) and had a model be taken into account, since they can increase the surgical for end stage liver disease (MELD) - sodium (Na) of 21 risk. Possible differential diagnoses include: Complicated points. The pain was referred to the left iliac fossa, with umbilical, inguinal or postoperative incisional hernias, an intensity of 10/10. It was associated to low back pain acute cholecystitis, spontaneous bacterial peritonitis, pep- with radicular stigmata (primarily S1).
    [Show full text]
  • 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.
    [Show full text]
  • High Risk Percutaneous Endoscopic Gastrostomy Tubes: Issues to Consider
    NUTRITIONINFLAMMATORY ISSUES BOWEL IN GASTROENTEROLOGY, DISEASE: A PRACTICAL SERIES APPROACH, #105 SERIES #73 Carol Rees Parrish, M.S., R.D., Series Editor High Risk Percutaneous Endoscopic Gastrostomy Tubes: Issues to Consider Iris Vance Neeral Shah Percutaneous endoscopy gastrostomy (PEG) tubes are a valuable tool for providing long- term enteral nutrition or gastric decompression; certain circumstances that complicate PEG placement warrant novel approaches and merit review and discussion. Ascites and portal hypertension with varices have been associated with poorer outcomes. Bleeding is one of the most common serious complications affecting approximately 2.5% of all procedures. This article will review what evidence exists in these high risk scenarios and attempt to provide more clarity when considering these challenging clinical circumstances. INTRODUCTION ince the first Percutaneous Endoscopic has been found by multiple authors to portend a poor Gastrostomy tube was placed in 1979 (1), they prognosis in PEG placement (3,4, 5,6,7,8). This review Shave become an invaluable tool for providing will endeavor to provide more clarity when considering long-term enteral nutrition (EN) and are commonly used these challenging clinical circumstances. in patients with dysphagia following stroke, disabling motor neuron diseases such as multiple sclerosis and Ascites & Gastric Varices amyotrophic lateral sclerosis, and in those with head The presence of ascites is frequently viewed as a and neck cancer.They are also used for patients with relative, if not absolute, contraindication to PEG prolonged mechanical intubation, as well as gastric placement. Ascites adds technical difficulties and the decompression in those with severe gastroparesis, risk for potential complications (see Table 1).
    [Show full text]
  • Intestinal and Multiple Organ Transplantation 1679
    1678 TRANSPLANT ATION euglycemia and survive longer than 200 islets in allogeneic and xenogeneic diabetic hosts. Transplant Proc 1993; 25:953-954. 67. Gotoh M, Maki T, Satomi S, et al: Immunological characteristics of purified islet grafts. Transplantation 1986; 42j387. 68. Klima G, Konigsrainer A, Schmid T, et al: Is the pancreas reo jected independently of the kidney after combined pancreatic­ renal transplantation? Transplant Proc 1988; 20:665. 69. Prowse 5J, Bellgrau D, Lafferty KJ: Islet allografts are destroyed by disease recurrence in the spontaneously diabetic BB rat. Di­ abetes 1986; 35:110. 70. Markmann JF, Posselt AM, Bassiri H, et al: Major-histocompat­ ibility-complex restricted and nonrestricted autoil1'\mune effec­ tor mechanisms in BB rats. Transplantation 1991; 52:662-667. 71. Navarro X, Kennedy WR, Loewenson RB, et al: Influence of pancreas transplantation on cardiorespiratory reflexes, nerve conduction, and mortality in diabetes mellitus. Diabetes 1990; 39:802. 72. Weber q, Silva FG, Hardy MA, et al: Effect of islet transplan­ tation on renal function and morphology of short- and long­ term diabetic rats. Transplant Proc 1979; 11:549. 73. Gotzche 0, Gunderson HJ, Osterby R: Irreversibility of glomer­ ular basement membrane accumulation despite reversibility of renal hypertrophy with islet transplantation in early diabetes. Diabetes 1981; 30:481. 74. Fung H, Alessini M, Abu-Elmagd K, et al: Adverse effects asso­ ciated with the use ofFK 506. Transplant Proc 1991; 23:3105. 75. Tzakis AG: Personal communication, 1991. I CHAPTER 185 Figure 185-1. Cluster allograft (shaded portion), including the liver, pancreas, and duodenal segment of small intestine. (From Starzl TE, Todo S.
    [Show full text]
  • Management of Autoimmune Liver Diseases After Liver Transplantation
    Review Management of Autoimmune Liver Diseases after Liver Transplantation Romelia Barba Bernal 1,† , Esli Medina-Morales 1,† , Daniela Goyes 2 , Vilas Patwardhan 1 and Alan Bonder 1,* 1 Division of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA; [email protected] (R.B.B.); [email protected] (E.M.-M.); [email protected] (V.P.) 2 Department of Medicine, Loyola Medicine—MacNeal Hospital, Berwyn, IL 60402, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-617-632-1070 † These authors contributed equally to this project. Abstract: Autoimmune liver diseases are characterized by immune-mediated inflammation and even- tual destruction of the hepatocytes and the biliary epithelial cells. They can progress to irreversible liver damage requiring liver transplantation. The post-liver transplant goals of treatment include improving the recipient’s survival, preventing liver graft-failure, and decreasing the recurrence of the disease. The keystone in post-liver transplant management for autoimmune liver diseases relies on identifying which would be the most appropriate immunosuppressive maintenance therapy. The combination of a steroid and a calcineurin inhibitor is the current immunosuppressive regimen of choice for autoimmune hepatitis. A gradual withdrawal of glucocorticoids is also recommended. Citation: Barba Bernal, R.; On the other hand, ursodeoxycholic acid should be initiated soon after liver transplant to prevent Medina-Morales, E.; Goyes, D.; recurrence and improve graft and patient survival in primary biliary cholangitis recipients. Unlike the Patwardhan, V.; Bonder, A. Management of Autoimmune Liver previously mentioned autoimmune diseases, there are not immunosuppressive or disease-modifying Diseases after Liver Transplantation.
    [Show full text]
  • Spontaneous Bacterial Peritonitis: Recent Guidelines and Beyond R Wiest,1 a Krag,2 a Gerbes3
    Downloaded from gut.bmj.com on May 31, 2012 - Published by group.bmj.com Recent advances in clinical practice Spontaneous bacterial peritonitis: recent guidelines and beyond R Wiest,1 A Krag,2 A Gerbes3 1Department for visceral surgery INTRODUCTION prognosis in various cohorts of patients with SBP and medicine, University Spontaneous bacterial peritonitis (SBP) is the most are summarised in figure 1 and include age,16 20 Hospital Bern, Switzerland 18 20 23 16 18 2 frequent and life-threatening infection in patients Child score, intensive care, nosocomial Department of 18 24 25 Gastroenterology, Hvidovre with liver cirrhosis requiring prompt recognition origin, hepatic encephalopathy, elevated 26 University Hospital, and treatment. It is defined by the presence of >250 serum creatinine and bilirubin, lack of infection Copenhagen, Denmark polymorphonuclear cells (PMN)/mm3 in ascites in resolution/need to escalate treatment and culture 3 e Klinikum of the University of the absence of an intra-abdominal source of infec- positivity27 29 as well as the presence of bacter- Munich, Munich, Germany tion or malignancy. In this review we discuss the aemia30 and CARD15/NOD2 variants as a genetic fl 31 Correspondence to current opinions re ected by recent guidelines risk factor. It is important to stress in this context Professor Dr Reiner Wiest, (American Association for the Study of Liver that the only factors that are modifiable in this Department for visceral surgery Diseases, European Association for the Study of the scenario are timely diagnosis and effective first-line and medicine, University Liver, Deutsche Gesellschaft für Verdauungs- und treatment. Hospital Bern, 3010 Bern, 1e4 Switzerland; Stoffwechselkrankheiten), with particular focus [email protected] on controversial issues as well as open questions Bacterial translocation (BT) and pathophysiology that need to be addressed in the future.
    [Show full text]
  • 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.
    [Show full text]