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Title: Gastroenterology


1
Gastroenterology
2
Gastroesophageal Reflux
  • Most common reason for the use of antacids in the
    United States
  • 5-10 of Americans have heartburn daily
  • Cause multi-factorial, decreased L.E.S pressure
    is seen approximately 25 of the time when the
    reflux occurs
  • Drugs known to lower LES pressure calcium
    channel blockers, beta-agonists, anti-cholinergic
    medications, alphablockers, theophylline,
    progesterone, morphine, dopamine and nitrates

3
Gastroesophageal Reflux (Contd)
  • Esophageal complications esophagitis, bleeding,
    stricture, Barretts esophagus, adenocarcinoma
  • Extra-esophageal complications Laryngitis,
    Laryngeal carcinoma , Tracheal stenosis, Asthma,
    Aspiration pneumonitis, Chronic cough, Dental
    erosion
  • Diagnostic Tests pH monitoring (gold standard),
    esophogram,manometry,PPI Trial
  • Treatment Lifestyle Modification, Pharmacologic
    Therapy, Antireflux surgery

4
Esophagitis
  • Can be caused by an infection or irritation of
    the esophagus
  • Infection can occur because of bacteria, viruses
    (herpes), fungi, and yeast (Candida)
  • A primary condition or secondary to
    gastroesophageal reflux, hiatal hernia, vomiting,
    surgery, medications, Lye, Radiation
  • Symptoms Dysphagia, Odynophagia, Heart Burn
    (reflux), oral lesions (herpes)

5
Esophagitis (Contd)
  • TestsBarium esophagogram, Acid perfusion tests,
    Culture, Esophagoscopy with/without biopsy (gold
    standard)
  • Treatment depends on the specific cause
  • Complications severe discomfort, swallowing
    difficulty, malnutrition /dehydration, scarring,
    Barrett's esophagus, cancer

6
Barretts Esophagus
  • Esophageal squamous epithelium replaced with
    metaplastic columnar epithelium
  • Incidence up to 10/lifetime
  • Variable
  • Usually men gt55
  • GERD commonly present
  • Dx EGD with biopsy
  • Treatment
  • Treat reflux aggressively PPI
  • Surveillance for dysplasia
  • No dysplasia q 3-5 years
  • Dysplasia confirm with expert pathologist/
  • GI specialist
  • Mortality reduction - unproven

7
Varices
  • Bleeding accounts for 1/3 of all deaths in
    patients with cirrhosis and portal hypertension
  • Preventive beta blockers, banding, evaluation
    for liver transplantation
  • Treatment  banding, balloon tamponade, TIPS,
    Octreotide and vasopressin, Portacaval shunts
  • Complications recurrent bleeding, hypovolemic
    shock, esophageal stricture, encephalopathy,
    infection

8
Zenker's Diverticulum
  • The most common type of esophageal diverticulum,
    etiology is uncertain
  • More common in men than women, usually presents
    over 60 years of age
  • Symptoms dysphagia, regurgitation, coughing,
    aspiration, unexplained weight loss, halitosis,
    feeling of food sticking
  • Diagnosis endoscopy, barium esophagography
  • Treatment
  • Recurrent symptomatic
  • Usually surgery

9
Mallory-Weiss Syndrome
  • Incidence is 4 out of 100,000
  • From prolonged and forceful vomiting, coughing or
    convulsions, excess ETOH
  • Sx hematemesis and/or melena secondary to
    mucosal tears at the GE junction
  • Resolves within 10 days without special
    treatment, recurrent bleeding uncommon
  • Occasionally may need EGD to stop bleeding.
    Surgery is rarely required

10
Achalsia
  • A diffuse motor disorder incomplete relaxation
    of the L.E.S and absence of peristalsis (this
    cardinal finding sufficient to make a diagnosis
    of achalasia)
  • Symptoms dysphagia, regurgitation, and the
    classic x-ray finding of gradual tapering of
    distal esophagus(birds beak)
  • Esophageal manometry (gold standard)
  • Treatment
  • Esophageal dilatation
  • Surgery
  • Botulinum toxin injections into L.E.S

11
Cause of Nonanginal Chest Pain
  • 0-1 features of typical Angina
  • Substernal
  • Worse with exertion/emotion
  • Relieved by rest/NTG
  • Nonspecific or "psychogenic" chest pain,
    sometimes occurs acutely as panic disorder, is
    the leading cause of non-anginal chest pain
  • MAY COEXIST WITH CAD

12
Cause of Nonanginal Chest Pain (Contd)
  • May be attributable to musculoskeletal problems,
    respiratory causes of chest pain
  • Esophagitis, peptic ulcer, gallbladder disease,
    pancreatitis, and hiatal hernia may lead to chest
    discomfort
  • Gall bladder disease has long been thought to be
    capable of inducing various types of anginal and
    nonanginal chest pain
  • Mitral valve prolapse may be associated with
    symptoms of non-anginal chest pain

13
Dysphagia
  • Common in aging persons, approximately 7 to 10
    percent of adults older than 50 years
  • Oropharyngeal dysphagia dysfunctional transfer
    from pharynx to esophagus
  • Stroke is the leading cause of oropharyngeal
    dysphagia
  • Esophageal dysphagia disordered peristaltic
    motility(Neuromuscular Disorder) or (Mechanical
    Obstruction)

14
Dysphagia (Contd)
  • Neuromuscular Motility disorder progressive
    difficulty in swallowing solid food and liquids,
    Achalasia and scleroderma are the leading
    motility disorders
  • Mechanical Obstruction typically dysphagia of
    solid food but not liquids (carcinomas,
    strictures and Schatzki's rings)
  • Patient history will identify 80 - 85 of the
    causes of dysphagia. (Consider malignancy)
  • Further testing may be indicated to confirm a
    diagnosis or to establish risk of aspiration

15
Odynophagia
  • A strong feeling of burning, squeezing pain while
    swallowing
  • Dysphagia may or may not be present
  • May have symptoms of chest pain, food stuck in
    the throat, or heaviness or pressure in the neck
    or upper chest
  • May be caused by destruction of the mucous
    membrane, infection, chemicals, or motor
    disorders of the esophagus

16
Upper GI Bleeding
  • Hematemesis and/or melena (black tarry stools)
  • Hematochezia (maroon or bright red blood per
    rectum) when massive
  • Multiple etiologies PUD, Mallory-Weiss,
    Variceal, Carcinoma
  • Diagnosis-clinical presentation
  • /- NG lavage

17
Upper GI Bleeding (Contd)
  • PUD bleeding risk stratity by EGD for
    rebleeding
  • Active bleeding 90
  • Visible vessel 50
  • Clot 25-30
  • Flat spot/clean ulcer 3-10
  • With low risk may be safely fed/discharge

18
Upper GI Bleeding (Contd)
  • Endoscopic treatment
  • Thermal coagulation (heater probe, gold probe,
    BICAP)
  • Injective therapy (epinephrine)
  • Combination therapy commonly used for high risk
    causes i.e. active bleeding
  • Endoclips
  • Antisecretory therapy
  • PPI unproven benefit
  • Omeprazole i.v. decreases rebleeding after
    endoscopic treatment
  • H2 blockers disappointing results
  • Octreotide reduce rebleeding RR 0.5
  • 50-100 mcg bolus, 25-50 mcq/hr for up to 3 days

19
Upper GI Bleeding (Contd)
  • Surgery
  • Secondary prevention of recurrent bleeding UI
    caps
  • Incidence 1/month
  • Treatment of H. pyloni
  • Avoid risk factors
  • Maintenance H2B or PPI for high risk

20
Dyspepsia
  • 25 percent (13 to 40 percent) of population
  • The most common cause of dyspepsia is
    functional or nonulcer, dyspepsia (specific
    etiology is not identified)
  • 3 Options endoscopy all patients, trial of
    empiric antisecretory drug therapy, testing for
    H. pylori infection followed by Rx if positive
  • Ranking of options is controversial, and no
    definitive recommendations can be made
  • 1/3 - 1/2 spontaneous resolution of symptoms

21
Nausea and Vomiting
  • Definition
  • Nausea-unpleasant sensation of being about to
    vomit
  • Retching-similar to vomiting without expulsion of
    gastric contents
  • Regurgitation-effortless return of gastric
    contents typical of GERD
  • Vomiting-forceful expulsion
  • Vomiting
  • Controlled humoral/neuronal stimuli to CNS
    chemo receptor trigger zone and nucleus tractus
    solitorius

22
Nausea and Vomiting (Contd)
  • Selected different Dx
  • Rumination
  • Daily, effortless regurgitation of undigested
    foods usually in mentally impaired children (and
    adults) reassurance and behavioral therapy are
    primary treatment
  • Eosinophilic Gastroenteritis
  • Rare disorder eosinophilic infiltration of the
    gut suspect in history of allergy, peripheral
    eosinophilia responsive to steroids
  • Cyclic Vomiting Syndrome
  • Repeated episodes of nausea/vomiting (hours/days)
    separate by symptom-free episodes treatment
    supportive

23
Diagnostic Approach to Nausea and Vomiting
  • Guided by history and exam examples
  • Early morning vomiting in female pregnancy
  • Abdominal tenderness and feculent emesis bowel
    obstruction
  • Vertigo labyrinthitis
  • Addition of new medications drug induced
  • Enamel erosion, calluses on dorsum on hands
    bulimia

24
Diagnostic Approach to Nausea and Vomiting
(Contd)
  • If history/exam doesnt suggest specific cause,
    evaluate for
  • Low grade intestinal obstruction CT, small
    bowel series
  • Metabolic causes TSH, Free T4, Glucose, CaH
  • Mucosal abnormalities EGD with bx
  • Psychogenic, bulimic, rumination

25
Treatment
  • Emetogenic chemotherapy
  • Prn
  • Lorazepam 1-3 mg q 4-6 hr
  • Prochlorperazine (15 mg spansule bid) or
  • Metoclopramide (30 mg qid) diphenhydramine (50
    mg qid) for restlessness
  • Oral 5-HT3 antagonist (Ondanestron 16 mg/d or
    Granisetron 2 mg/d Dexamethasone 20 mg
    orally/i.v.
  • Motion sickness/vestibular antihistamines
  • Postoperative and drug induced
  • 5 HT3 antagonist
  • Dopamine antagonist

26
Acute Pancreatitis Etiology
  • Etiology
  • Gallstones 45
  • Alcohol 35
  • Others
  • Post ERCP
  • Tumor
  • Drugs
  • Anatomic variation
  • Cystic Fibrosis
  • Symptoms
  • Acute upper abdominal pain steady
  • Alcohol related 1-3 days after binge

27
Acute Pancreatitis Etiology (Contd)
  • Tests
  • Amylase
  • Usually elevated for 3-5 days and gt3x upper
    limits of normal
  • Elevated in nonpancreatic processes (cirhosis,
    renal failure, alcoholism, intestinal infarct,
    fallopian tubes)
  • Lipase
  • Elevation occur earlier and last longer than
    Amylase
  • ABD US/CT-ABD with contrast (R/O necrosis as
    nonenhancing areas gt3 cm in size

28
Acute Pancreatitis Treatment
  • Early ERCP for gallstone pancreatitis and then
    elective cholecystectomy usually prior to
    hospital discharge
  • Pain control Meperdine traditional but no
    clinical benefit over Morphone or Fentanyl
  • Prophylactic antibodies reduce mortality in
    severe necrotizing pancreatitis (gt30 Necrosis)
  • Imipenem, fluoroquinolones
  • Enteral Feeds
  • Considered safe
  • May reduce complications
  • High protein, low fat (Peptamen)
  • Start slow
  • 100-300 cc fluids q 4hr day 1
  • Same volume add nutrients day 2

29
Complications of Acute Pancreatitis
  • Pseudocyst or abscess formation
  • Gastrointestinal hemorrhage secondary to
    ulceration or varices
  • Right-side hydronephrosis
  • Splenic rupture or hematoma
  • Shock
  • A.R.D.S.
  • Acute renal failure secondary to ATN
  • Psychosis
  • Metabolic abnormalities including hyperglycemia
    and hypocalcemia

30
Chronic Pancreatitis
  • Most common etiology alcohol
  • Diagnosis based on clinical criteria in the
    setting or recurrent abdominal pain assisting by
    imaging
  • Pain epigastirc, radiates to back postprandial
  • Pancreatic insufficiency 90 of pancreas usually
    destroyed. Loose, greasy, foul smelling stools
    that are difficult to flush. Diabetes is usually
    insulin requiring
  • Amylase/Lipase commonly normal
  • Imaging U.S., CT Scan, MRI, ERCP, Endoscopic
    U.S., Plain flims

31
Chronic Pancreatitis - Pain Control
  • Mostly the art of medicine not science
  • Non-specific
  • Analgesics
  • Anti-depressants
  • Decrease intra pancreatic pressure
  • Inhibition of gastric acid secretion H2B/PPI
    reduce PH stimuli to pancreatic secretion
  • Pancreatic enzymes
  • Nerve blocks
  • Endoscopic stents for structures
  • Surgery decompression, denervation, resection

32
Celiac Sprue
  • Chronic malabsorption disease of the small
    intestine in genetically suspectable individuals
  • USA 1/250
  • Serologic tests for antibodies identify most
    patients
  • Antiendomysial
  • Anti gliadin

33
Celiac Sprue (Contd)
  • Distal duodenal biopsy is the gold standard for
    the diagnosis of celiac disease
  • Common signs/symptoms
  • Malabsorption weight loss
  • Fe deficient anemia
  • Osteoperosis (in men)
  • Abdominal pain
  • Treatment strict gluten-free diet
  • No wheat, rye, barley

34
Acute Diarrhea
  • More than 3 times per day, less than 14
    days,usually spontaneously resolves
  • Bacterial, viral, parasitic, non-infectious
  • Rehydrate, Diet, anti-diarrhetics
  • Antimicrobials for persistent shigella,
    salmonella or campylobacter infections
    especially immunocompromised, artificial
    prostheses, persistent parasitic causes
  • Limit antimicrobials in immunocompetent
    individuals (antimicrobial resistance)

35
Acute Diarrhea (Contd)
  • With fever and blood (invasive pathogen)
  • Shigella, Campylobacter, Salmonella
  • Leukocytes in feces, fecal culture, thick
    bloodsmear for malaria
  • Antibiotics for serious,persistent infection
  • No fever or blood(Non-invasive pathogens)
  • Enterotoxic E.coli, Giardia, Rotavirus, Norwalk,
    Parasites
  • Traveler's diarrhea (85 of cases)
  • No leukocytes in feces, fecal culture (low yield)
  • Correct dehydration, spontaneous recovery except
    treat parasite infection

36
Chronic Diarrhea
  • Lasts for more than 2 weeks
  • Infectious Parasites Cryptosporidium,
    Cyclospora, Entamoeba, Giardia,microsporidia
    Bacteria Campylobacter, Clostridium difficile,
    E.coli, Listeria, Salmonella, Shigella, Viral
    HIV, rotavirus, Norwalk
  • NonInfectious drugs, crohns disease, endocrine
    diseases, food additives (sorbitol, fructose, and
    others), food allergies, GI surgery or radiation,
    tumors, intestinal ischemia, lactose, caffeine,
    ETOH

37
Chronic Diarrhea (Contd)
  • Usually related to functional disorders like
    irritable bowel syndrome, celiac disease, or
    inflammatory bowel disease
  • Should consider testing if patients are febrile
    or have bloody stool
  • Avoid antimotility agents in bloody diarrhea
    especially when caused by E. coli O157H7, (risk
    of hemolytic-uremic syndrome)
  • Endoscopy more specific than radiographic studies
    in detecting the etiology of chronic diarrhea

38
Constipation
  • Less than three stools per week
  • Usually from excess absorption of water from slow
    passage in the colon
  • Possible causes, motility disorder and pelvic
    floor disorder, endocrine disorder
  • Older people, not a result of aging but chronic
    illnesses, diet, neurologic and psychiatric,
    medicines, lack of exercise
  • In infancy and childhood most constipation is
    functional rather than organic

39
Constipation (Contd)
  • Most common cause inadequate fiber content
  • No clear agreement to which tests are usefull
  • Organic, metabolic, endocrine disease need to be
    excluded
  • Treatment of constipation is symptomatic
  • Eat regular, eight (8-oz)glasses of water daily,
    regular exercise, move bowels when urged
  • Best Tx, a diet rich in fiber (30 - 35 grams
    daily)
  • Avoid stimulant laxatives, a suppository or
    gentle enema is better

40
Intestinal Ischemia
  • Acute mesenteric ischemia mortality rates 71,
    diagnosis before infarction is most important
    factor to improve outcome
  • Chronic mesenteric ischemia (intestinal angina)
    is characterized by postprandial abdominal pain,
    and marked weight loss
  • Colon ischemia the most common form, most cases
    do not have a recognizable cause, most resolve
    spontaneously, usually has an excellent prognosis

41
Lower GI Bleeding
  • Causes bleeding diverticulum, carcinoma,
    angiodysplasia, Crohns disease, ulcerative
    colitis, dysentery,hemorrhoids, fissure
  • Beets may simulate hematochezia
  • Most causes are initially self limited
  • Colonoscopy with epinephrine injection or bipolar
    coagulation if severe hematochezia
  • Angiography or nuclear medicine studies can be
    useful to localize lower GI bleeding

42
Occult GI Bleeding
  • Positive fecal occult blood test, and/or iron
    deficiency anemia (IDA), without visible blood
  • More commonly a bleeding source in the upper GI
    tract (29 to 56 percent) than in the lower
    gastrointestinal tract (20 to 30 percent)
  • Likelihood of finding a bleeding source higher
    in patients with IDA (61 to 71) than those with
    positive FOBT (48 to 53 percent)
  • Colonoscopy and upper endoscopy remain the major
    investigative methods

43
Obscure GI Bleeding
  • Bleeding of unknown origin that persists or
    recurs after negative endoscopic evaluation
  • Requires evaluation of the small bowel, may
    require repeat upper and lower endoscopy
  • Biopsy to detect celiac sprue, a cause of IDA
  • Push Enteroscopy, Enteroclysis, Radioisotope
    bleeding scans (high false-positives)
  • Angiography can identify highly vascular
    nonbleeding lesions such as angiodysplasia and
    neoplasms
  • Wireless capsule endoscopy for small bowel
    lesions (Given Imaging)

44
Anal / Rectal Disease
  • Most frequent causes of anorectal bleeding are
    hemorrhoids, fissures and polyps
  • High index of suspicion for cancer
  • Evaluation of bright red blood per rectum
  • lt40 and obvious source no additional eval
  • 40-50 sigmoidoscopy
  • gt50 colonsocopy

45
Anal / Rectal Disease (Contd)
  • Pruritus ani is more likely to represent a
    chronic itch/scratch cycle than infection
  • Any pruritic lesion that persists after adequate
    treatment should be biopsied
  • Anal pain with fever and inability to void
    signals perineal sepsis and is an emergency
  • Biopsy all "warts" before ablative treatment
    Verrucous carcinoma can appear to be a wart
  • Cancer can coexist with benign lesions, so
    complete assessment is necessary

46
Crohns Disease
  • Can involve entire GI tract, mouth to the anus,
    terminal ileum is most commonly affected, 2 - 3
    have upper GI involvement
  • Corticosteroids should not be used as long-term
    agents to prevent relapse
  • Azathioprine/mercaptopurine have demonstrable
    maintenance benefits after inductive therapy with
    corticosteroids
  • Severe cases with failure to improve within 7-10
    days with intensive management consider surgery

47
Ulcerative Colitis
  • Most serious complications Toxic Megacolon (20
    mortality rate)
  • Risk of colon cancer doubles every 10 years, 5
    will develop colon cancer
  • If entire colon involved, risk of cancer may be
    as great as 32 times the normal rate
  • Yearly colonoscopy with biopsy for patients who
    have had the disease gt than 8-10 years
  • Surgery to remove entire colon is curative,
    25-40 eventually undergo this procedure

48
Microscopic Colitis
  • A cause of chronic diarrhea, its etiology is
    unknown, (Collagenous and Lymphocytic Colitis)
  • Biopsy is the only way to make the diagnosis (the
    colon appears normal during endoscopy)
  • In pts with chronic diarrhea and a normal
    colonoscopy (without biopsy) or barium enema, 10
    will have microscopic colitis
  • Flexible sigmoidoscopy with multiple biopsies
    from the left colon will detect almost all
    patients with microscopic colitis and may
    preclude the need for a colonoscopy

49
Irritable Bowel Syndrome (IBS)
  • The most widely accepted diagnostic criteria for
    IBS are the Rome II Criteria
  • Rome II Criteria
  • 12 weeks or more, need not be consecutive in
    preceding 12 months of abdominal discomfort/pain
    with 2 of the following
  • Relieved with defecation
  • Change in frequency of stool
  • Change in form

50
Irritable Bowel Syndrome (IBS) (Contd)
  • Diagnosis can be based upon typical clinical
    findings
  • Doesnt require exhausting diagnostic evaluation
  • Blood count, sed rate, FOBT, O/P stool, and if
    gt50 colonic evaluation
  • Red flags (weight loss, anemia, occult GI
    bleeding, nocturnal awakening) are inconsistent
    with diagnosis
  • Prevalence 10-20 and only 10-30 of those seek
    medical care

51
Irritable Bowel Syndrome (IBS) (Contd)
  • Psychological stress exacerbates symptoms in
    everyone not just IBS
  • Medication for symptom control
  • Pain/floating antispasmodic, TCA, SSRI
  • Constipation fiber
  • Diarrhea loperamide
  • Alosetron (Lotronex) women severe diarrhea
    predominant
  • Tegaserod (Zelnorm) women severe constipation
    predominant

52
Cirrhosis
  • The eleventh leading cause of death by disease in
    the United States
  • In the United States, chronic alcoholism and
    hepatitis C are the most common causes
  • Three criteria (1) diffuse disease, (2) the
    presence of fibrosis and (3) replacement of
    normal architecture by abnormal nodules
  • Diagnosis should include the cause of the liver
    disease

53
Cirrhosis (Contd)
  • Maintain a balanced diet containing 1 to 1.5 g of
    protein per kg per day
  • Premalignant condition, risk of hepatocellular
    carcinoma
  • Hepatocellular carcinoma is a leading cause of
    death in patients with cirrhosis
  • Once cirrhosis has developed, hepatitis C is the
    most common cause of hepatocellular Ca
  • Screening with alpha-fetoprotein and
    ultrasonography every six months

54
Ascites
  • In patients with cirrhosis and Ascites
  • Ascites is the most common form of clinical
    decompensation
  • Carries a poor prognosis, 50 mortality within 2
    years
  • Prone to spontaneous bacterial peritonitis
    (diagnostic tap is mandatory if suspect
    infection)
  • Patients with new-onset ascites or clinical
    deterioration should undergo paracentesis
  • Evaluation for liver transplantation should be
    considered in all patients

55
Ascites (Contd)
  • Follow a sodium-restricted diet
  • Diuresis, with spironolactone (Aldactone) as
    first-line therapy and occasional use of a
    supplemental loop diuretic
  • Diagnosis of spontaneous bacterial peritonitis
    (SBP) heralds advanced liver disease
  • Antibiotic prophylaxis for SBP as a preventive
    strategy cannot be definitely recommended
  • TIPSS (Transjugular intrahepatic portal-systemic
    stent-shunt) is an efficacious treatment for
    patients with refractory ascites

56
Hemochromatosis
  • The most common single-gene disorder in the U.S.
    white population (one in 250 to 300)
  • HFE gene test to confirm the diagnosis, and
    screen adult family members
  • Many patients have no manifestations
  • Liver biopsy remains the "gold standard" for
    assessing the degree of fibrosis
  • Risk of hepatocellular carcinoma is 200 times
    higher (risk of cancer persists even after
    excess iron stores have been depleted)

57
Hepatitis A
  • Seroprevalence in US 38
  • Children lt5 yr 10 gt50 yr 74
  • Accounts for 20-40 of all viral hepatitis
  • Spread fecal-oral route maternal-fetal
    transmission not reported
  • Usually results in acute, self-limited illness or
    asymptomatic infection (majority of cases)
  • Fulminant disease more common when co-infected
    with HBV or HCV, especially when older
  • Labs
  • ALT gt AST usually gt1000 IU/dl
  • Bilirubin gt10 mg/dl is common
  • IgM anti-HAV-gold standard for diagnosis

58
Hepatitis A (Contd)
  • Treatment - supportive
  • 85 full clinical/biochemical recovery in 3 mo.
  • Prevention handwashing
  • Survive on fingertips up to 4 hours
  • Household dilute bleach (1100 dilution)
  • Postexposure proplyaxis
  • Immune globulin and HAV vaccination usually
    administrated together
  • Immune globulin effective within 2 weeks of
    exposure
  • Vaccine recommended for higher risk groups
    (chronic liver disease, occupational risk,
    children in states with higher risk (gt2x national
    average))

59
Hepatitis B
  • Global public health problem
  • 300 million HBV carriers
  • 250,000 deaths yearly
  • In USA 0.1-2 prevalence of HBV carriers
  • Transmission
  • Perinatal
  • 90 if mother HBeAg positive (30 if negative)
  • Infection at or after birth
  • C/S doesnt prevent
  • Breastfeeding doesnt increase risk

60
Hepatitis B (Contd)
  • Transfusion
  • Decreasing 2 routine screening by HBsAg and
    anti-HBC
  • Risk 163,000 during window period
  • Sexual
  • 50 of cases in U.S.
  • Nosocomial
  • Most commonly transmitted blood-borne virus more
    common from patient to health care provider
  • Percutaneous exposure and risk of infection
  • HBV 6-30
  • HCV 0-7
  • HIV 0.3

61
Hepatitis B (Contd)
  • Treatment for chronic HBV infections
  • Considered when HBsAg gt6 months, evidence of
    active virus replication (HBeAg and HBV DNA
    positive) and active liver disease (chronic
    hepatitis on biopsy, elevated ALT)
  • Interferon Therapy
  • 12-24 weeks in doses of 5 Million Units
    (MU)/daily or 10 Million Units (MU) 3x/week
  • Pegylated interferon may be helpful
  • Results
  • Supresses HBV replication (? HBV-DNA, HBeAg)
  • Improvement in liver disease (normal ALT)
  • Prevention of cirrhosis, hepatocellular caranoma,
    survival (SCANT DATA)

62
Hepatitis C
  • Acute process often asymptomatic prevalence in
    U.S. 1.8
  • 80 develop chronic hepatitis
  • 10-15 of these develop cirrhosis of which 10
    may develop decompensated disease or
    hepatocellular carcinoma (HCC)
  • Most common cause of chronic liver disease and
    most frequent indication for liver transplant

63
Hepatitis C (Contd)
  • Transmission
  • Primarily through exposure to infected blood
  • anti-HCV screening started in 1992
  • Heterosexual monogamous relationships
  • Risk low 0-0.5/year
  • May not be higher than general population
  • Dont need barrier protection
  • Perinatal
  • 2 when EIA positive, 7 when HCV RNA positive
  • NO data on preventive by C/S
  • Breastfeeding doesnt appear to transmit
  • Test infant at 2 and 6 months for HCV RNA and at
    15 months for anti-HCV

64
Hepatitis C (Contd)
  • Lab Testing
  • EIA (3rd generation) sensitivity and specificity
    99 - excellent test
  • Qualitative HCV RNA test should follow to
    confirm acute or chronic HCV infection
  • Quantitative HCV RNA test (qPCR, bDNA) provides
    important prognosis information to treatment
  • Screen for HCC despite lack of data
  • AFP and hepatic U.S. screening commonly done on
    cirrhotics, not all HCV positive patients

65
Hepatitis C (Contd)
  • Treatment
  • Highest response with Pegylated Interferon and
    Ribavarin
  • Genotype 1
  • Treat for 48 weeks if minimum of 2 log decrease
    detected at 12 weeks
  • Ribavarin 1000-1200 mg usual dose
  • Genotype 2,3
  • Treat 24 wk
  • Ribavarin 800 mg

66
Cholangitis
  • 85 of cases due to impacted stone in duct
  • Charcots Triad (RUQ abdominal pain, fever and
    jaundice) present in 70 of cases
  • Diagnosis increased WBC, increased LFTS, blood
    cultures, ERCP(gold standard), cholangiogram,
    ultrasound
  • Management ERCP with stone removal, Antibiotics
    that cover gram-negative organisms, consider
    cholecystectomy

67
Gallbladder Disease
  • Acute Cholecystitis
  • 90 of cases - gallstone obstructs the cystic
    duct,10 of cases - absence of gallstones
    (acalculous cholecystitis)
  • Diagnostic tests Ultrasound (most useful),
    Cholescintigraphy, Abdominal CT scanning
  • Management definitive therapy -cholecystectomy
  • Pregnant patient -conservative therapy
    (antibiotics and supportive care)

68
Gallbladder Disease (Contd)
  • Choledocholithiasis
  • 15 of patients with gallbladder stones have
    stones in common bile duct
  • Tests ERCP (gold standard), cholangiography
  • Ultrasound visualizes about 50 of common bile
    duct stones, can detect CBD dilatation in 75 of
    cases
  • Complications cholangitis, acute pancreatitis
  • Management stone removal by ERCP, early
    cholecystectomy
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