| Treating
and Preventing Complications of Cirrhosis |
Certified for 0.25
Category 1 AMA Credit
Sponsored by the University
of Alabama School of Medicine
Division of Continuing Medical Education
| Release Date:
May 2, 2005 |
Expiration
Date: May 2, 2008 |
| TARGET
AUDIENCE: |
| Primary
care physicians |
| ABSTRACT:
|
| Earlier diagnosis
of cirrhosis and its complications and earlier interventions
make more therapeutic options available. |
| OBJECTIVES:
|
| The reader will
understand the major complications of cirrhosis and be aware
of appropriate preventive and therapeutic options. |
| Top of Page |
| FACULTY: |
| GUEST EDITOR: |
| Brendan
M. McGuire, MD
Associate Professor of Medicine
Department of Gastroenterology
The University of Alabama at Birmingham
Birmingham, Alabama |
| DISCLOSURE: |
| In accordance
with the Accreditation Council for Continuing Medical Education
Standards for Commercial Support, Dr. McGuire discloses the
following: grants and research support Protective Life Inc.
and Roche. |
| CME
PARTICIPATION: |
| To participate
in this program for CME credit, please review the objectives
before beginning the program. Complete the course and the self-assessment
test before May 2, 2008 to receive CME credit. Your certificate
will then be available online. This process should take approximately
15 minutes. |
| ACCREDITATION:
|
| The University
of Alabama School of Medicine is accredited by the Accreditation
Council for Continuing Medical Education (ACCME) to provide
continuing medical education for physicians.
The University of Alabama School
of Medicine designates this educational activity for a maximum
of 0.25 Category 1 credit toward the AMA Physician's Recognition
Award. Each physician should claim only those hours of credit
that he/she actually spent in the activity.
The boards of nursing in many
states, including Alabama, recognize Category 1 continuing
medical education courses as acceptable activities for the
renewal of license to practice nursing. |
| Top of Page |
| Introduction: |
|
Preventing and treating complications
of cirrhosis early may provide better longitudinal care and
more therapeutic opportunities for the 400,000 Americans who
often have silent symptoms for years before diagnosis.
"Despite recent advances
in cirrhosis treatment approaches, esophageal varices and
hepatocellular carcinoma remain frequent, and potentially
fatal, complications," UAB hepatologist Brendan M. McGuire,
MD, says. "In fact, 1 of every 25 patients with hepatitis
C and cirrhosis may develop hepatocellular carcinoma. Intervening
as early as possible dramatically increases available treatment
options." |
| Delaying
Disease Progression: |
| Finding
strategies that help prevent or delay progression of cirrhosis
is one of McGuire's goals as principal investigator of the
UAB Interdisciplinary Cirrhosis Clinic, where patients have
access to the latest diagnostic tools, treatments, and clinical
trials. The clinic provides patient education extending from
basic information about the liver and how it functions to
treatments for potential complications and ways to prevent
or delay disease progression. The clinic evaluates patients
for hepatitis, hepatocellular carcinoma, variceal bleeding,
spontaneous bacterial peritonitis, hepatopulmonary syndrome,
hepatorenal syndrome, and liver transplantation. A planned
Web site will soon allow patients access to detailed information
about the clinic and its services.
"Early symptoms of cirrhosis
include itching, fatigue, loss of appetite, anorexia, abdominal
pain, nausea, and weakness. Patients may present with clinical
features such as jaundice, variceal bleeding, ascites, edema,
or hepatic encephalopathy," McGuire says. "Yet,
by the time cirrhosis is diagnosed, patients are typically
suffering from advanced forms of disease. As cirrhosis progresses,
potential complications include hepatocellular carcinoma,
hepatopulmonary syndrome, and hepatorenal syndrome."
|
| Top of Page |
| Diagnosing
Cirrhosis: |
| Cirrhosis
can be definitively diagnosed by liver biopsy, McGuire says.
"However, biopsy may be contraindicated in patients with
significant ascites or coagulopathy. Cirrhosis should be considered
in the presence of splenomegaly or a history and physical
exam revealing suspicious symptoms. A presumptive diagnosis
can be made on the basis of computed tomography scan, ultrasound,
or magnetic resonance imaging."
Cirrhosis
usually progresses as a chronic, insidious process from long-term
alcohol abuse, chronic viral infection such as hepatitis B
or C, metabolic disorders such as hemochromatosis or Wilson
disease, or autoimmune diseases, including autoimmune hepatitis,
primary biliary cirrhosis, or primary sclerosing cholangitis.
Outside the United States, cirrhosis is among the leading
causes of death and is commonly caused by hepatitis B. Closer
to home, one of the leading causes of cirrhosis today is hepatitis
C, which has infected nearly 4 million Americans, according
to the Centers for Disease Control and Prevention. |
| Top of Page |
| Complications
of Cirrhosis: |
| "As
liver disease progresses, changes occur in the cirrhotic patient's
hemodynamic circulatory state. These circulatory disturbances
include portal hypertension and portosystemic shunting and
increases in cardiac output, heart rate, and effective circulating
blood volume, along with decreases in systemic vascular resistance
and arterial blood pressure. These alterations contribute
to many of the cardiac, pulmonary, and renal complications
associated with cirrhosis," McGuire says.
One common complication cirrhotic
patients develop is ascites. Treatment options include dietary
salt restriction, diuretics such as furosemide or spironolactone,
abdominal paracentesis, peritoneo-venous shunts, or transjugular
intrahepatic portosystemic shunts. While McGuire generally
advises a 2000 mg per day salt-restricted diet, he says limiting
salt is extremely difficult, and patients must read nutritional
labels carefully to measure sodium intake.
"Another complication of
cirrhosis is hepatic encephalopathy, a reversible neuropsychiatric
syndrome with metabolic abnormalities but no major neuropathic
findings. The syndrome is treated with lactulose and/or antibiotics
to purge the gut of ammonia and decrease colonic concentration
of ammonia-producing bacteria," he says.
Esophageal varices will occur
in up to 70% of cirrhotic patients with no prior upper gastrointestinal
bleed (Hepatology. 1997;25:1346-1350 and Semin Liver
Dis. 1999;19:475-505). The complication is fatal for nearly
one third of cirrhotic patients who develop it, yet, variceal
bleeding rates could drop from 70% to 40% if patients are
medically managed with nonspecific b-blocker therapy (Gastroenterology.
2002;122[6]:1620-1630).
"All cirrhotic patients
should be evaluated for varices with esophagogastroduodenoscopy.
If no varices are seen or only small varices are present,
the test should be repeated in 2 years. Patients with clinical
signs of cirrhosis and those with significant varices should
be treated with nonselective b-blockers, such as propranolol
or nadolol, to prevent initial bleeding or rebleeding of ruptured
varices. Nadolol is less lipophilic, is not metabolized by
the liver, and does not cross the blood-brain barrier, so
it is usually better tolerated than other nonselective b-blockers,"
McGuire says.
Mononitrates have also been used
to decrease portal pressures but can cause more systemic vasodilation
and are associated with increased mortality in cirrhotic patients
aged 50 years and older.
In patients with cirrhosis,
hepatorenal syndrome may occur as hyperdynamic circulatory
changes progress. "Hepatorenal syndrome occurs in about
one fifth of cirrhotic patients with tense ascites,"
McGuire says. "The renal arteries constrict, and the
kidneys inappropriately retain fluid despite systemic fluid
overload. Prognosis for people with hepatorenal syndrome is
poor, and liver transplantation is the only proven treatment."
Cirrhotic patients also are at
risk for hepatopulmonary syndrome, a triad of portal hypertension,
intrapulmonary vasodilation, and hypoxemia. "Hepatopulmonary
syndrome occurs in up to 20% of patients with cirrhosis. It
is diagnosed by excluding major intrinsic cardiopulmonary
disease and documenting intrapulmonary vasodilation with contrast
echocardiography and/or perfusion lung scanning and hypoxemia
by arterial blood gases. Liver transplantation reverses intrapulmonary
vasodilation and hypoxemia," he says. |
| Top of Page |
| Hepatitis
C-induced Cirrhosis: |
| In 2004,
the number of Americans who died with hepatitis C-induced
cirrhosis exceeded the total number of liver transplants.
"Many clinics have considered patients with hepatitis
C-induced cirrhosis poor candidates for treatment with peginterferon
and ribavirin," McGuire notes. "We would like to
change the hepatitis C management paradigm by aggressively
treating patients who will benefit most from therapy. The
UAB Interdisciplinary Cirrhosis Clinic has a staff of seven
hepatologists, strong clinical research programs, and partners
with UAB's nationally recognized liver transplant program,
making the clinic an ideal treatment environment for these
patients," he says. |
| Top of Page |
| Liver
Transplantation: |
| "A
healthy lifestyle and adherence to medical management may
delay cirrhotic progression, but ultimately, many patients
will face liver transplantation as their only option,"
McGuire says. UAB's Liver Transplant Program has performed
more than 1000 liver transplants in its 16-year history, and
the program's 90% 1-year survival rate is higher than the
national average. In fact, a significant number of patients
are celebrating 10 years or more of posttransplant survival. |
| Top of Page |
| Multidisciplinary
Expertise: |
| "Our clinic team includes gastroenterologists, hepatologists, transplantation surgeons, neuropsychologists, nutritionists, physical medicine and rehabilitation specialists, and support staff," McGuire says. "We provide a complete evaluation to screen for and treat potentially life-limiting cirrhotic complications, maximizing quality of life by improving physical and mental well-being." |
| Top of Page |
| For
more information: |
Dr. Brendan McGuire
1-800-UAB-MIST
mist@uabmc.edu
|
|
| Self-Assessment
Test: |
| To
apply for 0.25 Category 1 credit, complete the self-assessment
test and you should receive an online certificate immediately. |
| To
take the test click here! |
|