An Introduction to the Acid-Peptic Disorders Mark Feldman, MD.
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Transcript of An Introduction to the Acid-Peptic Disorders Mark Feldman, MD.
![Page 1: An Introduction to the Acid-Peptic Disorders Mark Feldman, MD.](https://reader035.fdocuments.us/reader035/viewer/2022070408/56649e675503460f94b62a24/html5/thumbnails/1.jpg)
An Introduction to the An Introduction to the Acid-Peptic DisordersAcid-Peptic Disorders
Mark Feldman, MD
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Outline of talk
• Physiology
• Pathophysiology
• Clinical Features• GERD• PUD
• Therapy
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Regions and gland areas of the gastric mucosaRegions and gland areas of the gastric mucosa
HCl (HCl (acidacid) &) & pepsinpepsin I are I are produced inproduced in thethe OXYNTIC OXYNTIC GLAND AREAGLAND AREAby parietal cellsby parietal cellsand chief cells,and chief cells,respectivelyrespectively
(source of gastrin)(source of gastrin)
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Oxyntic gland area: Oxyntic gland area: acid-secreting parietal cellsacid-secreting parietal cells
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Acid-pepsin interactionsAcid-pepsin interactions
Pepsinogens
hydrochloric acid
Pepsins(pepticactivity)
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The proton pump of the parietal cell The proton pump of the parietal cell and its and its αα and and ββ chains chains
Activated PPI site
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Activation of Proton Pump Activation of Proton Pump Inhibitor (PPI) in Parietal CellInhibitor (PPI) in Parietal Cell
Basal-lateral Membrane
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apicalmembrane
basolateralmembrane
Cl-
Cl-
ATPase
K+
K+
HCO3 -
CO2 + H2O
H+ + HCO3-
CA
H+
P A R I E T A L C E L L
H2CO3
anionexchanger
cytosol
lumen
KCl symport
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Histamine-producing ECL Histamine-producing ECL (enterochromaffin-like) cells(enterochromaffin-like) cells
adjacent to parietal cells adjacent to parietal cells
ParietalParietalCellCell
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P ECL
G
gastrin
Antral mucosa
Hista- mine
HCl
Oxynticmucosa
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2-Receptor Model for 2-Receptor Model for Parietal Cell ActivationParietal Cell Activation
• Histamine-2 receptor:– generates cAMP signal– major trigger is gastrin released by food protein
working via ECL cell and histamine release– blockers: cimetidine, ranitidine, famotidine, and nizatidine
• Acetylcholine receptor:– generates Ca++ signal– major trigger is “cephalic” phase– blockers: atropine and related anticholinergics
note: PPIs block final step of H+ secretion and block both paths
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Activation of the parietal cell’s acid pumps Activation of the parietal cell’s acid pumps by acetylcholine (Ach) and Histamineby acetylcholine (Ach) and Histamine
•Fusion of tubulovesicles with canaliculus, plus•Insertion of KCl symporter (conductance) into canaliculus
M3R H2R (inactive pumps)
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Gastrin’s time-related effects on ECL cells Gastrin’s time-related effects on ECL cells acting via CCK-2 (CCK-B) receptorsacting via CCK-2 (CCK-B) receptors
©Copyright Science Press Internet Services
ECLECL
HDC = histidine decarboxylase
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ECL cell hyperplasia 2° to hypergastrin-ECL cell hyperplasia 2° to hypergastrin-emia in a patient with a gastrinoma (ZES)emia in a patient with a gastrinoma (ZES)
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Pathophysiology of the Pathophysiology of the acid-peptic diseasesacid-peptic diseases
AGGRESSIVE FACTORSAGGRESSIVE FACTORS
• AcidAcid• PepsinPepsin
DEFENSIVE FACTORSDEFENSIVE FACTORS
• Bicarbonate/ mucusBicarbonate/ mucus
• ProstaglandinsProstaglandins
• Clearance of acid via Clearance of acid via motor functionmotor function
• Adequate blood supply / Adequate blood supply / oxygenationoxygenation
• Cell turnover and Cell turnover and restitutionrestitution
• No inflammationNo inflammation
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Strategies for therapy of Strategies for therapy of the acid-peptic diseasesthe acid-peptic diseases
AGGRESSIVE FACTORSAGGRESSIVE FACTORS
• Reduce acidity and Reduce acidity and hence peptic activityhence peptic activity– antacidsantacids
– anticholinergicsanticholinergics
– histamine-2 histamine-2 blockersblockers
– proton pump proton pump inhib- inhib- itors (PPIs)itors (PPIs)
DEFENSIVE FACTORSDEFENSIVE FACTORS
• Stop NSAIDsStop NSAIDs
• Stop smokingStop smoking
• Prostaglandin analogProstaglandin analog• Pro-motility agent Pro-motility agent (GER)(GER)
• Maintain blood Maintain blood pressure/ hi Opressure/ hi O22 sat. sat.
• Treat inflammation Treat inflammation when presentwhen present
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The common acid-peptic diseasesThe common acid-peptic diseases
• GERD, and its complications– normal acid-pepsin secretion, but excessive
acid exposure to the esophageal epithelium
• PUD, and its complications– DU: acid-pepsin hypersecretion common, but
not universal; heterogeneous disease– GU: acid-pepsin secretion normal usually,
implying impaired defensive mechanisms
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The acid-peptic diseasesThe acid-peptic diseases
• GERD– uncomplicated: heartburn– complications:
• esophageal: stricture; bleeding; adenocarcinoma
• airway: sore throat; throat clearing; laryngitis; asthma
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How common is heartburn?How common is heartburn?
WOMENWOMEN
ages 25-34 48%
ages 35-44 40%
ages 45-54 47%
ages 55-64 30%
ages 65-74 40%
MENMEN
42%
53%
39%
39%
35%
( %’s refer to ANY heartburn)( %’s refer to ANY heartburn)
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How common isHow common is frequent heartburn? frequent heartburn?
WOMENWOMEN
ages 25-34 16%
ages 35-44 14%
ages 45-54 22%
ages 55-64 14%
ages 65-74 20%
MENMEN
14%
26%
20%
17%
17%
(frequent means at least weekly)
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Beverages and heartburnBeverages and heartburn
The 5 WORSTThe 5 WORST::– Red Wine
– Grapefruit juice
– Orange juice
– Coffee
– V8/Tomato juice
The 5 BESTThe 5 BEST::– Water
– Prune juice
– Skim milk
– Peach nectar
– Gatorade
(M Feldman, C Barnett. Gastroenterology 108:125, 1995)
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Who is predisposed Who is predisposed to heartburn/GERD?to heartburn/GERD?
• Pregnant women (25% have daily heartburn)
• People with hiatal hernias
• People who smoke
• People who drink alcohol to excess
• People with acid hypersecretion (e.g., ZES)
• People who are not infected with H. pylori
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Endoscopic appearance of Endoscopic appearance of reflux esophagitisreflux esophagitis
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Barium esophagram of Barium esophagram of esophageal peptic strictureesophageal peptic stricture
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Endoscopic appearance of Endoscopic appearance of Barrett’s esophagusBarrett’s esophagus
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Gross pathologic appearance of Gross pathologic appearance of esophageal adenocarcinomaesophageal adenocarcinoma
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Treatment of GERD: Step Up RxTreatment of GERD: Step Up Rx
• Step 1: lifestyle modifications: dietary (food avoidance), mechanical (gravity, avoid tight clothes, etc.); weight loss if obese; smoking cessation; avoid overeating or late snacks
• Step 2: over-the-counter chewable antacid tablets or liquids, H2 blockers (Pepcid, Tagamet, Zantac, Axid); or combinations of the two (Pepcid Complete)
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Treatment of GERD (cont’d)Treatment of GERD (cont’d)
• Step 3: Prescription doses of H2 blockers or PPIs (Prilosec, Prevacid, Nexium, Protonix, Aciphex)
• Step 4: Add a pro-motility drug to help clear gastric contents from the esophagus, such as metoclopramide (Reglan)
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Treatment of GERD (cont’d)Treatment of GERD (cont’d)
• Step 4?: New endoscopic treatments are under evaluation but long term value and safety is ???– Radiofrequency application (Stretta)
– Suturing/sewing
– Injection therapies
• Step 5: Surgery, ideally through a laparascope (minimally-invasive surgery)
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Treatment of GERD: Step Down Treatment of GERD: Step Down
• Step 1: Life style modifications plus once a day PPI
• Step 2: Step up if failure; try to step down if success (but maintenance Rx usually requires dose needed to heal and induce remission)
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The acid-peptic diseasesThe acid-peptic diseases
• GERD
• PUD, and its complications– uncomplicated: pain (“gastralgia”)– complications: bleeding, perforation, obstruction
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Sir William Osler’s description Sir William Osler’s description of the pain of peptic ulcerof the pain of peptic ulcer
Pain is perhaps the most constant and distinctive feature of ulcer. It varies greatly in character; it may be only a gnawing or burning sensation, which is particularly felt when the stomach is empty, and it is relieved by taking food, but the more characteristic form comes on in paroxysms of the most intense gastralgia, in which the pain is not only felt in the epigastrium, but radiates to the back and to the sides.
THE PRINCIPLES AND PRACTICE OF MEDICINE, 1909THE PRINCIPLES AND PRACTICE OF MEDICINE, 1909
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Risk factors for PUDRisk factors for PUD
• Helicobacter pylori gastritis• Aspirin, even “low” cardiovascular doses*• NSAIDS*• Cigarette smoking*• Family history (genetics) • Acid hypersecretion (e.g., ZES)• Emotional distress
* reduce mucosal prostaglandins
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Benign gastric ulcer along the Benign gastric ulcer along the greater curvaturegreater curvature
UlcerUlcer
radiating radiating foldsfolds
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Benign gastric ulcer along the Benign gastric ulcer along the lesser curvaturelesser curvature
UlcerUlcer
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Typical radiographic features Typical radiographic features of a benign gastric ulcerof a benign gastric ulcer
ulcer
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Malignant gastric ulcer Malignant gastric ulcer occurring within a massoccurring within a mass
ulcer
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Endoscopic view: Endoscopic view: gastric ulcergastric ulcer
©Copyright Science Press Internet Services
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Endoscopic view of a Endoscopic view of a benign gastric ulcerbenign gastric ulcer
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Endoscopic view of a gastric ulcerEndoscopic view of a gastric ulcer
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Bleeding gastric ulcerBleeding gastric ulcerwith “visible vessel”with “visible vessel”
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Enoscopic stigmata of Enoscopic stigmata of recent gastric ulcer hemorrhage recent gastric ulcer hemorrhage
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Ulcer rebleeding rate based on Ulcer rebleeding rate based on endoscopic stigmataendoscopic stigmata
• Actively bleeding 90%*
• Visible vessel 50%*
• Adherent clot 10-15%*
• Dots and spots 3%-5%
• Clean base 1% or less
* Endoscopic therapy recommended
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Pyloric outlet obstruction & Pyloric outlet obstruction & peripyloric ulcer disease peripyloric ulcer disease
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Obstructing benign gastricObstructing benign gastriculcer in pyloric channel ulcer in pyloric channel
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Pyloric outlet obstruction Pyloric outlet obstruction & peri-pyloric ulcer disease& peri-pyloric ulcer disease
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Typical radiographic featuresTypical radiographic features of a duodenal ulcer of a duodenal ulcer
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Ulcer
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Typical radiographic featuresTypical radiographic features of a duodenal ulcer of a duodenal ulcer
©Copyright Science Press Internet Services
Ulcer
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Endoscopic view: duodenal ulcerEndoscopic view: duodenal ulcer
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Duodenal Ulcer associated with enteric-coated aspirinDuodenal Ulcer associated with enteric-coated aspirin
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Perforated duodenal ulcerPerforated duodenal ulcer
©Copyright Science Press Internet Services free air
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Therapy of PUDTherapy of PUD• Eliminate H. pylori, if present• Discontinue aspirin, NSAIDs, and/or coxibs, if
applicable and if possible• Counseling and referral to smoking cessation
program, if applicable
• Proton pump inhibitor or H2-blocker
• Treat ulcer complications endoscopically (e.g., bleeding or GOO) plus a PPI (IV or PO) or surgically (e.g., perforation or failure of endoscopic therapy)
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Quiz: Which disorder(s) are risk Quiz: Which disorder(s) are risk factors for acid-peptic disease?factors for acid-peptic disease?• Cystic fibrosis
• Sclerosing cholangitis
• Meckel’s diverticulum
• Chronic basophilic leukemia
• None of the above
• All of the above
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Which of the following patients should undergo EGD, and why?
• A 48 year old woman with longstanding heartburn easily controlled with life style modifications and OTC ranitidine.
• A 60 year old man with new onset dyspepsia and no “alarm” symptoms.
• A 45 year old man with dyspepsia and a duodenal bulbar ulcer on upper GI series.
• A 45 year old man with dyspepsia and a pre-pyloric gastric ulcer on upper GI series.
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Gastrin stimulates parietal cells Gastrin stimulates parietal cells via neighboring ECL cellsvia neighboring ECL cells
Serum Gastrin
ECL CCK2R
Histamine
H2R (PC)
cAMP(±Ca)
Gastric Acid Secretion
CCK2R (PC)
Ca
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P2
ECL2
DS
1
G
gastrin
DS
1 C C K
Antral mucosa
Duodenal mucosa
H
HCl
Oxynticmucosa
S
IS, somatostatin
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Typical radiographic features Typical radiographic features of a benign gastric ulcer of a benign gastric ulcer
ulcer
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Soll’s 3-receptor parietal cell modelSoll’s 3-receptor parietal cell model