Methods And Biopsy Protocols
IN
Upper Gastrointestinal Endoscopy
Dr. DINESH THAPA
3rd
year MDGP and EM Resident
Introduction
 Performed by passing a flexible endoscope
through the mouth into the esophagus,
stomach and duodenum
 Best method for examining the upper
gastrointestinal mucosa
 Superior for detection of gastric ulcers and
flat mucosal lesions, such as Barrett’s
esophagus and it permits directed biopsy
and endoscopic therapy
Language of the Wheels/Buttons
 Superior button-
 Suction
 Inferior button
 Insufflation of air
 Insufflation of water
 Big Wheel
 Towards you
 Upwards
 Small wheel
 Away from you
 To the right side
Endoscope Handling
Ambidextrous
 Left hand on control head
 Right hand on endoscopy shaft
The endoscopist controls the shaft
 Clockwise twist
 Anticlockwise twist
Navigate using
 Wheel movement
 Shaft movement
 Your body movement
Endoscopic Biopsy Forceps
 2 cup shaped jaws
 Round/ elliptical, serrated/ non
serrated
 Best to use forcep with
needle spike at the center
- to fix the mucosa
- Provide deeper biopsies
Cleaning and Disinfection
 Low-level disinfection
 Non-critical accessories Come in contact with intact skin
 Cameras and endoscopic furniture
 Sterilization
 Critical reusable accessories
 Which enters body cavities and vasculature or penetrate mucous membranes
 Biopsy forceps, sclerotherapy needles and sphincterotomes
 High- level disinfection
 Semi-critical accessories  which come into contact with mucous
membranes
 Endoscopes and esophageal dilators
Cleaning and Disinfection
 Manual disinfection
Soak the instrument and accessories in the chosen disinfectant
Glutaraldehyde – most popular disinfectant
The length of contact time needed for disinfection- 20 minutes
is commonly recommended
More prolonged soaking  known or suspected mycobacterial
disease
Peracetic acid, chlorine dioxide, sterox – have also been used
Golden Rules for Endoscopic Safety
• Do not push if you cannot see
• If in doubt, inflate and pull back
Esophagus
 Cervical esophagus
- from the upper esophageal sphincter/cricopharyngeal
sphincter (16 cm from incisors) to entry of the
esophagus into the chest
- Lower boundary not visible at endoscopy
 Intrathoracic part
- almost 20 cm long and ends when the esophagus
enters the abdominal cavity through diaphragm
- Approximately 38-40 cm from incisors
 Intra-abdominal part
- Ends at esophagogastric junction and the lower
esophageal sphincters
 Aortic constriction- at 25cm, the aorta crosses the
esophagus and appears as an external compression
Esophagus
 Esophagogastric junction
- defined endoscopically as the distal ends
of esophageal that meet the proximal
ends of gastric longitudinal mucosal folds
 Squamocolumnar junction ( Z-line)
- The junction of the squamous mucosa
and columnar mucosa
 Hiatus
- Opening in the diaphragm through
which esophagus passes from the
thoracic to the abdominal cavity
Stomach
Steps of Endoscopy
Steps of Endoscopy
Steps of Endoscopy
Cervical Esophagus
Steps of Endoscopy
Thoracic Esophagus
Steps of Endoscopy
Esophagogastric Junction
Steps of Endoscopy
Steps of Endoscopy
Steps of Endoscopy
Steps of Endoscopy
To advance through the body and into antrum
 Big wheel towards you (UP)
 Clockwise twist of shaft
 Push the scope
Steps of Endoscopy
Steps of Endoscopy
Steps of Endoscopy
Steps of Endoscopy
Steps of Endoscopy
J Maneuver
Big wheel fully towards you and Pull back
Steps of Endoscopy
Big wheel fully towards you along with shaft movement and
your body movement
360 degree panoramic view of cardia
Steps of Endoscopy
Enter the pylorus when it is at the centre and wide open
and scope is straight
Steps of Endoscopy
Enter 2nd
part: Do 3 maneuvers
Big wheel: towards U
Small wheel: away from U
Turn your body to right
Removing the instrument
Mucosal views are often optimal during instrument withdrawal
The proximal lesser curve, a potential “blind spot” merits
particular attention
Aspirate air from the stomach completely on withdrawal
Upper GI Endoscopy
Pathological Lesions
Mallory-Weiss Lesion and Boerhaave Syndrome
 Longitudinal superficial mucosal laceration
 Occurs primarily at the gastroesophageal
junction and may extend proximally to involve
the lower to mid-esophagus or distally to
involve the proximal portion of the stomach
 Frequently posterior
 Complete rupture of the esophagus is known
as Boerhaave syndrome
Eosinophilic esophagitis
 Endoscopic finding
- multiple esophageal rings, linear furrows,
white punctate exudate and strictures
 Biopsy
- 2 to 4 biopsies of the proximal
esophagus
- 2 to 4 biopsies of the distal esophagus
 Biopsies of the gastric antrum and
duodenum if there is suspicion of
eosinophilic gastroenteritis
Infectious esophagitis
 Endoscopic finding
- Ulcerations are numerous, punctate
and diffuse
 CMV infection – biopsies from the
base of the ulcers
 HSV infection - biopsies from the
base of the ulcers
 Esophageal candidiasis – biopsies
from affected areas + exfoliative
cytology
Gastroesophageal Reflux and Reflux Esophagitis
Endoscopic findings
 Erosions and ulcerations are usually few and distal
Indications for endoscopy
 For patients with GERD symptoms who also have alarm symptoms such as
• Dysphagia
• Weight loss
• Bleeding
• Vomiting
• Anemia
Diagnostic endoscopy should ideally be performed after PPIs have been
stopped for 2 weeks and perhaps as long as 4 weeks if possible
Gastroesophageal Reflux and Reflux Esophagitis
Esophageal biopsy should be taken to exclude other diagnosis, including
infectious etiologies and malignancy under the following condition
 Immunocompromised patients
 Irregular and deep ulceration
 Presence of mass lesion or nodularity
 Irregular or malignant appearing stricture
Biopsy
 Targeted biopsies of irregular mucosa
Modified Los Angeles Classification of GERD
Grade Description
A 1or more mucosal break no longer than 5
mm without continuation between mucosal
folds
B 1or more mucosal break longer than 5 mm
without continuation between mucosal fold
C 1 or more mucosal break that is continuous
between the tops of two or more mucosal
folds but that involves less that 75% of the
circumference
D 1or more mucosal break that involves at
least 75% of the esophageal circumference
Hiatial Hernia
 Persistent or recurrent herniation of
portion of the stomach through the
esophageal hiatus into the chest cavity
 Forward view
 Double-ring configuration
 Proximal ring is formed by the lower
esophageal sphincter(LES), the distal
ring by the esophageal hiatus
 The Z-line is within the dilated
segment, several centimeters above
the esophageal hiatus
 Retroflexed view
 Cardia does not close around
the endoscope
 Bell-shaped dilatation over the
cardia
 Folds radiating into the hernia
Barrett’s Esophagus
 Condition in which the squamous
epithelium of the distal esophagus is
substituted with columnar epithelium
 Prague classification of barrett’s esophagus-
both the maximal length (M) and the length
of the circumferential barrett segment (C)
are measured during endoscopy
 These numbers can then be used to track
the length of the barrett segment over time
Barrett’s Esophagus
 Protocol of seattle
 Barrett’s esophagus without dysplasia-
biopsies of 4 quadrants every 2 cm
 Barrett’s esophagus with low grade
dysplasia- biopsies of 4 quadrants every 1-2
cm
 Barrett’s esophagus with high grade
dysplasia- biopsies of 4 quadrants every 1 cm
Esophageal Varices
 Esophageal varices are
distended submucosal veins
that protrude into the
esophageal lumen
 Baveno classification of
esophageal varices
Size Description
Small Minimally elevated varices above
the esophageal mucosa surface
Medium Tortuous varices occupying less
than one third of the esophageal
surface
Large Varices that occupy more than
one third of the esophageal
surface
Esophageal Varices
Dagradi classification
Grade I : Variceal diameter less than 2 mm ,
disappear with esophageal lumen insufflation
Grade II: Varices of similar diameter, clearly visible in
the esophageal lumen
Grade III: Varices of 3-4 mm , prominent in the
esophageal lumen
Grade IV: Variceal diameter 5 mm or more , tortuous
Grade V: Red color signs
Gastritis
 Endoscopic features:
- Edema
- Exudate
- Erythema
- Erosion
- Hemorrhage
 Type A (Autoimmune gastritis)- Body
predominant
 Type B ( Bacterial gastritis)- Antral
predominant
Urease test
 1-2 biopsies: 5 cm proximal to the pylorus on
the lesser curvature near the angularis or on
the greater curve opposite the angularis
 Gastric biopsy material is tested for urease
activity by placing tissue in a medium
containing urea and pH reagent such as
phenolphthalein
 H pylori urease hydrolyzes urea liberating
ammonia  which produces an alkaline pH
resultant color change of the phenolphthalein
test medium
Urease test
 Sensitivity and specificity of tests are 90% to 95% and 95% to 100%
 Accuracy can be negatively affected by the blood in the stomach or
by the use of antibiotics, bismuth-containing compounds or acid
antisecretory drugs, especially PPIs.
 Negative urease test does not exclude Hp infection in an individual
taking antisecretory medication
 To improve sensitivity, stopping the potentially problematic
medication and delaying endoscopy for 2 weeks if possible
 H. pylori eradication should be documented 4 weeks after
completing antibiotics and atleast 7 days off antisecretory agents
Potential indication for gastroscopic biopsies
 Gastric erosions or ulcer
 Thick gastric folds
 Gastric polyp or mass
 For diagnosis of Hp infection
Sydney Protocol Biopsy
 5 biopsies
 1 from antrum 2-3 cm from pylorus lesser
curvature
 1 from antrum 2-3 cm from pylorus greater
curvature
 1 from the corpus 8 cm from the cardia less
curvature
 1 from the corpus 8 cm from the cardia greater
curvature
 1 biopsy from angular incisure, as atrophic
gastritis and intestinal metaplasia are related to
the development of gastric cancer and occur
most commonly at the incisure
Chronic atrophic gastritis
 Endoscopic findings
 Antral mucosal thinning
 Color and context change of the mucosa to red and
white( white colored mucosa with increased visibility of a
vascular pattern)
 Loss of rugal folds
 Atrophy caused by H. pylori infection tens to start from
antrum and extends to the body
 Tissue sampling
 7-12 biopsies: 4 quadrants biopsies from antrum(2-3 cm
proximal to pylorus), 2 from angularis, 4 from the mid corpus (
2 lesser curvature, 2 greater curvature), 2 from cardia
Gastric ulcer
 Repeat endoscopy to document healing at 8-
12 weeks should be performed for gastric
ulcer especially if present in body and fundus
 Multiple biopsies (>8) from the base and
edges if there is suspicion of malignancy
Forrest Classification
Sta
ge
Characteristi
cs
Re-
bleeding
Ia Active
bleeding
90%
Ib Oozing
hemorrhage
50%
IIa Nonbleeding
visible vessel
25-30%
IIb Adherent clot 10-20%
IIc Flat
pigmentation
7-10%
III Clean-based
ulcer
3-5%
Portal hypertensive gastropathy
Degree Portal hypertensive gastropathy
Mild Mosaic pattern without red spots
Moderate Typical mosaic pattern and infrequent red spots
Severe Numerous red spots
Gave syndrome
 Patchy, streaky, or reticular pattern of
erythema
 Mucosal hemorrhage
 Streaks radiating toward the antrum
( watermelon stripes)
 Fragile mucosa
Gastric Varices
 Convoluted vessels
protruding into the
lumen, sometimes with a
“ cluster of grapes”
appearance
 Encircling the cardia or
fundus, sometimes
found in the body and
antrum
Gastric Varices
 Most commonly used classification is Sarin’s
classification
 Gastric varices are categorized based on the
relationship with esophageal varices, as well
as by their location in the stomach
Duodenal ulcers
 more than 5 mm disruption of the
mucosal integrity of the duodenum
leading to a submucosal exposure
 Usually located at the duodenal
bulb
 Malignant duodenal ulcers are
extremely are
 Repeat endoscopy is warranted in
patients with duodenal ulcers if
symptoms persist despite medical
therapy or a complication is
suspected
Duodenal Biopsies
 Chronic diarrhea, iron deficiency anemia  suspicion of celiac
disease
 Tissue Sampling- 4-6 biopsies in the total from duodenal bulb
and distal duodenum
References
 Clinical Gastrointestinal Endoscopy, 2nd
edition
 Cotton and William’s Practical Gastrointestinal Endoscopy, 7th
edition
 Endoscopic mucosal tissue sampling, American society for
gastrointestinal endoscopy, 2013
Thank you

5 endoscopy (2).pptxppt on edoscopy techniques

  • 1.
    Methods And BiopsyProtocols IN Upper Gastrointestinal Endoscopy Dr. DINESH THAPA 3rd year MDGP and EM Resident
  • 2.
    Introduction  Performed bypassing a flexible endoscope through the mouth into the esophagus, stomach and duodenum  Best method for examining the upper gastrointestinal mucosa  Superior for detection of gastric ulcers and flat mucosal lesions, such as Barrett’s esophagus and it permits directed biopsy and endoscopic therapy
  • 3.
    Language of theWheels/Buttons  Superior button-  Suction  Inferior button  Insufflation of air  Insufflation of water  Big Wheel  Towards you  Upwards  Small wheel  Away from you  To the right side
  • 4.
    Endoscope Handling Ambidextrous  Lefthand on control head  Right hand on endoscopy shaft The endoscopist controls the shaft  Clockwise twist  Anticlockwise twist Navigate using  Wheel movement  Shaft movement  Your body movement
  • 5.
    Endoscopic Biopsy Forceps 2 cup shaped jaws  Round/ elliptical, serrated/ non serrated  Best to use forcep with needle spike at the center - to fix the mucosa - Provide deeper biopsies
  • 6.
    Cleaning and Disinfection Low-level disinfection  Non-critical accessories Come in contact with intact skin  Cameras and endoscopic furniture  Sterilization  Critical reusable accessories  Which enters body cavities and vasculature or penetrate mucous membranes  Biopsy forceps, sclerotherapy needles and sphincterotomes  High- level disinfection  Semi-critical accessories  which come into contact with mucous membranes  Endoscopes and esophageal dilators
  • 7.
    Cleaning and Disinfection Manual disinfection Soak the instrument and accessories in the chosen disinfectant Glutaraldehyde – most popular disinfectant The length of contact time needed for disinfection- 20 minutes is commonly recommended More prolonged soaking  known or suspected mycobacterial disease Peracetic acid, chlorine dioxide, sterox – have also been used
  • 8.
    Golden Rules forEndoscopic Safety • Do not push if you cannot see • If in doubt, inflate and pull back
  • 9.
    Esophagus  Cervical esophagus -from the upper esophageal sphincter/cricopharyngeal sphincter (16 cm from incisors) to entry of the esophagus into the chest - Lower boundary not visible at endoscopy  Intrathoracic part - almost 20 cm long and ends when the esophagus enters the abdominal cavity through diaphragm - Approximately 38-40 cm from incisors  Intra-abdominal part - Ends at esophagogastric junction and the lower esophageal sphincters  Aortic constriction- at 25cm, the aorta crosses the esophagus and appears as an external compression
  • 10.
    Esophagus  Esophagogastric junction -defined endoscopically as the distal ends of esophageal that meet the proximal ends of gastric longitudinal mucosal folds  Squamocolumnar junction ( Z-line) - The junction of the squamous mucosa and columnar mucosa  Hiatus - Opening in the diaphragm through which esophagus passes from the thoracic to the abdominal cavity
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20.
    Steps of Endoscopy Toadvance through the body and into antrum  Big wheel towards you (UP)  Clockwise twist of shaft  Push the scope
  • 21.
  • 22.
  • 23.
  • 24.
  • 25.
    Steps of Endoscopy JManeuver Big wheel fully towards you and Pull back
  • 26.
    Steps of Endoscopy Bigwheel fully towards you along with shaft movement and your body movement 360 degree panoramic view of cardia
  • 27.
    Steps of Endoscopy Enterthe pylorus when it is at the centre and wide open and scope is straight
  • 28.
    Steps of Endoscopy Enter2nd part: Do 3 maneuvers Big wheel: towards U Small wheel: away from U Turn your body to right
  • 29.
    Removing the instrument Mucosalviews are often optimal during instrument withdrawal The proximal lesser curve, a potential “blind spot” merits particular attention Aspirate air from the stomach completely on withdrawal
  • 30.
  • 31.
    Mallory-Weiss Lesion andBoerhaave Syndrome  Longitudinal superficial mucosal laceration  Occurs primarily at the gastroesophageal junction and may extend proximally to involve the lower to mid-esophagus or distally to involve the proximal portion of the stomach  Frequently posterior  Complete rupture of the esophagus is known as Boerhaave syndrome
  • 32.
    Eosinophilic esophagitis  Endoscopicfinding - multiple esophageal rings, linear furrows, white punctate exudate and strictures  Biopsy - 2 to 4 biopsies of the proximal esophagus - 2 to 4 biopsies of the distal esophagus  Biopsies of the gastric antrum and duodenum if there is suspicion of eosinophilic gastroenteritis
  • 33.
    Infectious esophagitis  Endoscopicfinding - Ulcerations are numerous, punctate and diffuse  CMV infection – biopsies from the base of the ulcers  HSV infection - biopsies from the base of the ulcers  Esophageal candidiasis – biopsies from affected areas + exfoliative cytology
  • 34.
    Gastroesophageal Reflux andReflux Esophagitis Endoscopic findings  Erosions and ulcerations are usually few and distal Indications for endoscopy  For patients with GERD symptoms who also have alarm symptoms such as • Dysphagia • Weight loss • Bleeding • Vomiting • Anemia Diagnostic endoscopy should ideally be performed after PPIs have been stopped for 2 weeks and perhaps as long as 4 weeks if possible
  • 35.
    Gastroesophageal Reflux andReflux Esophagitis Esophageal biopsy should be taken to exclude other diagnosis, including infectious etiologies and malignancy under the following condition  Immunocompromised patients  Irregular and deep ulceration  Presence of mass lesion or nodularity  Irregular or malignant appearing stricture Biopsy  Targeted biopsies of irregular mucosa
  • 36.
    Modified Los AngelesClassification of GERD Grade Description A 1or more mucosal break no longer than 5 mm without continuation between mucosal folds B 1or more mucosal break longer than 5 mm without continuation between mucosal fold C 1 or more mucosal break that is continuous between the tops of two or more mucosal folds but that involves less that 75% of the circumference D 1or more mucosal break that involves at least 75% of the esophageal circumference
  • 37.
    Hiatial Hernia  Persistentor recurrent herniation of portion of the stomach through the esophageal hiatus into the chest cavity  Forward view  Double-ring configuration  Proximal ring is formed by the lower esophageal sphincter(LES), the distal ring by the esophageal hiatus  The Z-line is within the dilated segment, several centimeters above the esophageal hiatus
  • 38.
     Retroflexed view Cardia does not close around the endoscope  Bell-shaped dilatation over the cardia  Folds radiating into the hernia
  • 39.
    Barrett’s Esophagus  Conditionin which the squamous epithelium of the distal esophagus is substituted with columnar epithelium  Prague classification of barrett’s esophagus- both the maximal length (M) and the length of the circumferential barrett segment (C) are measured during endoscopy  These numbers can then be used to track the length of the barrett segment over time
  • 40.
    Barrett’s Esophagus  Protocolof seattle  Barrett’s esophagus without dysplasia- biopsies of 4 quadrants every 2 cm  Barrett’s esophagus with low grade dysplasia- biopsies of 4 quadrants every 1-2 cm  Barrett’s esophagus with high grade dysplasia- biopsies of 4 quadrants every 1 cm
  • 41.
    Esophageal Varices  Esophagealvarices are distended submucosal veins that protrude into the esophageal lumen  Baveno classification of esophageal varices Size Description Small Minimally elevated varices above the esophageal mucosa surface Medium Tortuous varices occupying less than one third of the esophageal surface Large Varices that occupy more than one third of the esophageal surface
  • 42.
    Esophageal Varices Dagradi classification GradeI : Variceal diameter less than 2 mm , disappear with esophageal lumen insufflation Grade II: Varices of similar diameter, clearly visible in the esophageal lumen Grade III: Varices of 3-4 mm , prominent in the esophageal lumen Grade IV: Variceal diameter 5 mm or more , tortuous Grade V: Red color signs
  • 43.
    Gastritis  Endoscopic features: -Edema - Exudate - Erythema - Erosion - Hemorrhage  Type A (Autoimmune gastritis)- Body predominant  Type B ( Bacterial gastritis)- Antral predominant
  • 44.
    Urease test  1-2biopsies: 5 cm proximal to the pylorus on the lesser curvature near the angularis or on the greater curve opposite the angularis  Gastric biopsy material is tested for urease activity by placing tissue in a medium containing urea and pH reagent such as phenolphthalein  H pylori urease hydrolyzes urea liberating ammonia  which produces an alkaline pH resultant color change of the phenolphthalein test medium
  • 45.
    Urease test  Sensitivityand specificity of tests are 90% to 95% and 95% to 100%  Accuracy can be negatively affected by the blood in the stomach or by the use of antibiotics, bismuth-containing compounds or acid antisecretory drugs, especially PPIs.  Negative urease test does not exclude Hp infection in an individual taking antisecretory medication  To improve sensitivity, stopping the potentially problematic medication and delaying endoscopy for 2 weeks if possible  H. pylori eradication should be documented 4 weeks after completing antibiotics and atleast 7 days off antisecretory agents
  • 46.
    Potential indication forgastroscopic biopsies  Gastric erosions or ulcer  Thick gastric folds  Gastric polyp or mass  For diagnosis of Hp infection
  • 47.
    Sydney Protocol Biopsy 5 biopsies  1 from antrum 2-3 cm from pylorus lesser curvature  1 from antrum 2-3 cm from pylorus greater curvature  1 from the corpus 8 cm from the cardia less curvature  1 from the corpus 8 cm from the cardia greater curvature  1 biopsy from angular incisure, as atrophic gastritis and intestinal metaplasia are related to the development of gastric cancer and occur most commonly at the incisure
  • 48.
    Chronic atrophic gastritis Endoscopic findings  Antral mucosal thinning  Color and context change of the mucosa to red and white( white colored mucosa with increased visibility of a vascular pattern)  Loss of rugal folds  Atrophy caused by H. pylori infection tens to start from antrum and extends to the body  Tissue sampling  7-12 biopsies: 4 quadrants biopsies from antrum(2-3 cm proximal to pylorus), 2 from angularis, 4 from the mid corpus ( 2 lesser curvature, 2 greater curvature), 2 from cardia
  • 49.
    Gastric ulcer  Repeatendoscopy to document healing at 8- 12 weeks should be performed for gastric ulcer especially if present in body and fundus  Multiple biopsies (>8) from the base and edges if there is suspicion of malignancy
  • 50.
    Forrest Classification Sta ge Characteristi cs Re- bleeding Ia Active bleeding 90% IbOozing hemorrhage 50% IIa Nonbleeding visible vessel 25-30% IIb Adherent clot 10-20% IIc Flat pigmentation 7-10% III Clean-based ulcer 3-5%
  • 51.
    Portal hypertensive gastropathy DegreePortal hypertensive gastropathy Mild Mosaic pattern without red spots Moderate Typical mosaic pattern and infrequent red spots Severe Numerous red spots
  • 52.
    Gave syndrome  Patchy,streaky, or reticular pattern of erythema  Mucosal hemorrhage  Streaks radiating toward the antrum ( watermelon stripes)  Fragile mucosa
  • 53.
    Gastric Varices  Convolutedvessels protruding into the lumen, sometimes with a “ cluster of grapes” appearance  Encircling the cardia or fundus, sometimes found in the body and antrum
  • 54.
    Gastric Varices  Mostcommonly used classification is Sarin’s classification  Gastric varices are categorized based on the relationship with esophageal varices, as well as by their location in the stomach
  • 55.
    Duodenal ulcers  morethan 5 mm disruption of the mucosal integrity of the duodenum leading to a submucosal exposure  Usually located at the duodenal bulb  Malignant duodenal ulcers are extremely are  Repeat endoscopy is warranted in patients with duodenal ulcers if symptoms persist despite medical therapy or a complication is suspected
  • 56.
    Duodenal Biopsies  Chronicdiarrhea, iron deficiency anemia  suspicion of celiac disease  Tissue Sampling- 4-6 biopsies in the total from duodenal bulb and distal duodenum
  • 58.
    References  Clinical GastrointestinalEndoscopy, 2nd edition  Cotton and William’s Practical Gastrointestinal Endoscopy, 7th edition  Endoscopic mucosal tissue sampling, American society for gastrointestinal endoscopy, 2013
  • 59.