UGIB
Gada L.(MD) , internist,GI fellow, assistant professor of medicine ,SPHMMC
Feb.2016
Objective
• By the end of this session students will be able to:
– Define UGIB
– Evaluate patient with UGIB
– List DDx/identify causes
– Formulate basic diagnostic investigations
– Manage common cause of UGB
– Apply primary and secondary preventions of VB/PUD
3
Topic Out line
• Introduction:
• Etiology/DDx of UGIB:
• General management:
• Specific management:
• Summary:
4
• Define upper GI bleeding:
5
Definitions:
• Upper GI Bleeding = proximal to ligament of Treitz
• Hematemesis = vomiting blood
• Melena = passage of tarry or maroon stool
– Can be upper(90%) or lower
– Melena indicates blood has been present in the GI tract for at
least 14 h, and as long as 3–5 days.
• Hematochezia = Bright red blood per rectum
– Usually characteristic of colonic hemorrhage,or can be
upper(Severe UGIH).
6
Introduction
 Upper gastrointestinal bleeding (UGIB)-bleeding from UGI
proximal to the ligament of Treitz.
• Incidence 100 cases per 100,000 population per year.
• The incidence is twice as common in males as in women, and
increased with age.
• UGIB more common than LGIB.
7
Introduction…
• 80% self limiting , 20% rebleed --usu.in 72 hrs.
• Etiologies vary from place to place
• PUD is the most common cause of UGI
• Prognosis:depends on etiology and age/comorbidity
o Mortality = 5-10 %(OVER ALL).
o Ranges 1-30%
8
UGIB…
• What are the common causes of UGIB?
9
Most common causes of upper gastrointestinal
bleeding :
• Gastric and/or duodenal ulcers-PUD
• Esophagogastric varices with or without portal hypertensive
gastropathy
• Esophagitis
• Erosive gastritis/duodenitis
• Mallory-Weiss syndrome
• Angiodysplasia
• Mass lesions (polyps/cancers)
• Dieulafoy's lesion.
Cause of upper GI Bleeding
10
11
UGIB…
• What are the uncommon causes of UGIB?
12
Uncommon causes of UGIB
• Hemobilia= bleeding into bileduct and gallblader
• Hemosuccus pancreaticus
• Aortoenteric fistula
• Upper GI tumors
• Cameron lesion=ulcer from hiatal hernia
13
UGIB…
• HOW do you diagnose UGIB?
14
Diagnosis
• Hx/PE
• Lab. Profiles
• Endoscopy
• Imagings
– Barium study-c/I-in active bleeding
– Angiography
• Wireless video capsule endoscopy-PillCam.
15
UGIB….
• Outline General management approach to a patient with
UGIB:
16
Management of UGIB
• Urgent Hemodynamic evaluation and resuscitation:
• Initial Management:
– Assess severity:
– Tachycardia suggests 10% volume loss
– Orthostatic hypotension 20% loss,
– Shock 30% loss
17
Management -general
• Management of acute gastrointestinal bleeding:
– Monitor the pulse and blood pressure half-hourly.
– Establish intravenous access - central line if brisk bleed.
– Take blood for haemoglobin, urea, electrolytes, grouping and cross
matching (2 units initially).
– Give blood transfusion/colloid if necessary.
– Indications for blood transfusion are:
• (a) SHOCK (pallor, cold nose, systolic PB below 100 mmHg, pulse > 100 b.p.m.)
• (b) Haemoglobin < 10 g/dL in patients with recent or active bleeding.
– Oxygen therapy for shocked patients.
– Urgent endoscopy in shocked patients/liver disease.
– Continue to monitor pulse and BP.
– Re-endoscope for continued bleeding/hypovolaemia.
– PPI?
– Surgery if bleeding persists.
18
Cont…
• Resuscitation goals:
• High risk pts-HCt/HGB-30/1o
• Young and otherwise healthy patients should be transfused to
maintain their hemoglobin above 7 gm/dL.
• Patients with active bleeding and a coagulopathy ( INR >1.5)
or low platelet count (<50,000/micr.L) should be transfused
with fresh frozen plasma and platelets, respectively.
19
Nasogastric tube/NGT
• To remove particulate matter, fresh blood, and clots to
facilitate endoscopy and confirm an upper source of bleeding.
20
Factors That affect management/outcome:
• Age
• The amount of blood lost
• Signs of chronic liver disease on examination
• Evidence of co-morbidity:
• Cardiac failure
• Ischemic heart disease
• Renal disease and malignant disease.
• Shock
21
ESOPHAGOGASTRIC VARICES
• Esophagogastric varices develop as a consequence of portal
hypertension.
• What are the causes of PHTN?
– Pre hepatic
– Hepatic
– Post hepatic
22
Causes of PHTN
23
24
EV…
• A major complication ofportal hypertension -cirrhosis
– 10~30 % of UGIB
– 25 ~ 35%of patientswith cirrhosis
• Risk related to:
• Variceal size, appearanc “Red color signs”, Childs class and
location.
• 1/3 of deaths from cirrhosis
25
EV…
26
Outcomes
• Torrential
bleeding of varix!
• Acute Bleeding Episodes: < 48 hours
– 50 % stop spontaneously
– 1 episode → 30 % mortality
– Death: aspiration, sepsis, coma,
renal failure.
• The risk of rebleeding is high (60 to
70 %) until gastroesophageal varices
are obliterated.
• High Risk Period: < 6 weeks
– Rebleeding: 40 – 50 %-in the first
10 days.
27
Management of EVB
 Active variceal hemorrhage accounts for about one-third of all
deaths related to cirrhosis.
• Four major issues related to the prevention and treatment of
variceal hemorrhage:
 1.Prediction of patients at risk
 2.Prophylaxis against a first bleed
 3.Treatment of an active bleed
 4.Prevention of re-bleeding
28
PREDICTIVE FACTORS
— Clinical and physiologic factors are useful in predicting the risk
of variceal hemorrhage in patients with cirrhosis:
• Location of varices
• Size of varices:
• Appearance of varices
• Clinical features of the patient/Child class
• Variceal pressure.
29
Primary prophylaxis
• What is primary prophylaxis?
• How do you prevent VB(primary prophylaxis)?
30
Primary prophylaxis
• Goal :
• To reduce portal pressure / intravaricealpressure.
– Drugs that reduce portal venous flow or intrahepatic
vascularresistance have been used.
• Prophylactic propranolol or nadolol therapy is the only cost-
effective therapy.
• Endoscopic variceal ligation- beneficial for high-risk patients.
31
Treatment of active bleeding:
• There are three primary goals of management during the
active bleeding episode:
– Hemodynamic resuscitation
– Prevention and treatment of complications; and
– Treatment of bleeding.
32
Criteria for ICU Admission
• Institution specific
• In general:
– Ongoing hemodynamic instability despite IV fluids.
– Evidence of active bleeding: hematemesis, large
volume bloody lavage, hematochezia
– Significant comorbidities: ischemic liver, CAD
– Advanced age
33
Prophylactic antibiotic:
• Bacterial infections ; up to 20% of patients with cirrhosis,
hospitalized with UGIB:
– The most common sites are :
• urinary tract infections (approximately 12 to 29
percent)
• spontaneous bacterial peritonitis (7 to 23 percent)
• respiratory infections (6 to 10 percent), and
• primary bacteremia (4 to 11 percent).
– Antibiotics may also reduce the risk of recurrent bleeding.
34
Management of active bleeding…
 Vasopressin:
 Terlipressin -a synthetic vasopressin analogue with fewer
side effects and a longer half-life than vasopressin and thus
can be used in bolus form.
 SOMATOSTATIN AND ITS ANALOGS
– Syntheticanalogues; octreotide and vapreotid.
35
ENDOSCOPIC TREATMENT
• Endoscopic therapy is currently the definitive
treatment of choice for active variceal hemorrhage.
• Two forms of endoscopic treatment are commonly
used:
–Sclerotherapy-best for active bleeding
– variceal band ligation
36
Prevention of rebleeding/recurrent bleeding
• What is secondary prophylaxis?
• How can you prevent recurrent VB?
37
Prevention of recurrent bleeding
• Over 70 percent of patients experience recurrent variceal
hemorrhage within one year of their index bleed.
• The risk of rebleeding is greatest immediately after cessation
of active bleeding and then declines, reaching close to
baseline values by six weeks.
• Approximately 70 percent of all untreated patients die within
the first year after their initial variceal bleed
• Propranolol plus ligation..
38
Cont…
• AASLD GUIDELINES —
• The approaches recommended by the guidelines
(nonselective beta blockers, endoscopic variceal ligation,
transjugular intrahepatic portosystemic shunts, and liver
transplantation).
39
UGIB -PUD
 GU/DU
 There are four major risk factors for bleeding peptic ulcers:
– Helicobacter pylori infection
– Nonsteroidal antiinflammatory drugs (NSAIDs)
– Stress
– Gastric acid.
• The majority of patients with UGI bleeding due to peptic ulcer
disease will stop bleeding spontaneously and most will not
rebleed during hospitalization.
• Reduction or elimination of these risk factors reduces ulcer
recurrence and rebleeding rates.
40
Summery
• Causes of UGIB
• MX of VB
• MX of PUD(discussed)
41
The end
I Thank you
42
References
• UpTodate
• GUIDELINES
– AASLD/EASLD

upper gastro-intestinal bleeding slide ppt

  • 1.
    UGIB Gada L.(MD) ,internist,GI fellow, assistant professor of medicine ,SPHMMC Feb.2016
  • 2.
    Objective • By theend of this session students will be able to: – Define UGIB – Evaluate patient with UGIB – List DDx/identify causes – Formulate basic diagnostic investigations – Manage common cause of UGB – Apply primary and secondary preventions of VB/PUD
  • 3.
    3 Topic Out line •Introduction: • Etiology/DDx of UGIB: • General management: • Specific management: • Summary:
  • 4.
    4 • Define upperGI bleeding:
  • 5.
    5 Definitions: • Upper GIBleeding = proximal to ligament of Treitz • Hematemesis = vomiting blood • Melena = passage of tarry or maroon stool – Can be upper(90%) or lower – Melena indicates blood has been present in the GI tract for at least 14 h, and as long as 3–5 days. • Hematochezia = Bright red blood per rectum – Usually characteristic of colonic hemorrhage,or can be upper(Severe UGIH).
  • 6.
    6 Introduction  Upper gastrointestinalbleeding (UGIB)-bleeding from UGI proximal to the ligament of Treitz. • Incidence 100 cases per 100,000 population per year. • The incidence is twice as common in males as in women, and increased with age. • UGIB more common than LGIB.
  • 7.
    7 Introduction… • 80% selflimiting , 20% rebleed --usu.in 72 hrs. • Etiologies vary from place to place • PUD is the most common cause of UGI • Prognosis:depends on etiology and age/comorbidity o Mortality = 5-10 %(OVER ALL). o Ranges 1-30%
  • 8.
    8 UGIB… • What arethe common causes of UGIB?
  • 9.
    9 Most common causesof upper gastrointestinal bleeding : • Gastric and/or duodenal ulcers-PUD • Esophagogastric varices with or without portal hypertensive gastropathy • Esophagitis • Erosive gastritis/duodenitis • Mallory-Weiss syndrome • Angiodysplasia • Mass lesions (polyps/cancers) • Dieulafoy's lesion.
  • 10.
    Cause of upperGI Bleeding 10
  • 11.
    11 UGIB… • What arethe uncommon causes of UGIB?
  • 12.
    12 Uncommon causes ofUGIB • Hemobilia= bleeding into bileduct and gallblader • Hemosuccus pancreaticus • Aortoenteric fistula • Upper GI tumors • Cameron lesion=ulcer from hiatal hernia
  • 13.
    13 UGIB… • HOW doyou diagnose UGIB?
  • 14.
    14 Diagnosis • Hx/PE • Lab.Profiles • Endoscopy • Imagings – Barium study-c/I-in active bleeding – Angiography • Wireless video capsule endoscopy-PillCam.
  • 15.
    15 UGIB…. • Outline Generalmanagement approach to a patient with UGIB:
  • 16.
    16 Management of UGIB •Urgent Hemodynamic evaluation and resuscitation: • Initial Management: – Assess severity: – Tachycardia suggests 10% volume loss – Orthostatic hypotension 20% loss, – Shock 30% loss
  • 17.
    17 Management -general • Managementof acute gastrointestinal bleeding: – Monitor the pulse and blood pressure half-hourly. – Establish intravenous access - central line if brisk bleed. – Take blood for haemoglobin, urea, electrolytes, grouping and cross matching (2 units initially). – Give blood transfusion/colloid if necessary. – Indications for blood transfusion are: • (a) SHOCK (pallor, cold nose, systolic PB below 100 mmHg, pulse > 100 b.p.m.) • (b) Haemoglobin < 10 g/dL in patients with recent or active bleeding. – Oxygen therapy for shocked patients. – Urgent endoscopy in shocked patients/liver disease. – Continue to monitor pulse and BP. – Re-endoscope for continued bleeding/hypovolaemia. – PPI? – Surgery if bleeding persists.
  • 18.
    18 Cont… • Resuscitation goals: •High risk pts-HCt/HGB-30/1o • Young and otherwise healthy patients should be transfused to maintain their hemoglobin above 7 gm/dL. • Patients with active bleeding and a coagulopathy ( INR >1.5) or low platelet count (<50,000/micr.L) should be transfused with fresh frozen plasma and platelets, respectively.
  • 19.
    19 Nasogastric tube/NGT • Toremove particulate matter, fresh blood, and clots to facilitate endoscopy and confirm an upper source of bleeding.
  • 20.
    20 Factors That affectmanagement/outcome: • Age • The amount of blood lost • Signs of chronic liver disease on examination • Evidence of co-morbidity: • Cardiac failure • Ischemic heart disease • Renal disease and malignant disease. • Shock
  • 21.
    21 ESOPHAGOGASTRIC VARICES • Esophagogastricvarices develop as a consequence of portal hypertension. • What are the causes of PHTN? – Pre hepatic – Hepatic – Post hepatic
  • 22.
  • 23.
  • 24.
    24 EV… • A majorcomplication ofportal hypertension -cirrhosis – 10~30 % of UGIB – 25 ~ 35%of patientswith cirrhosis • Risk related to: • Variceal size, appearanc “Red color signs”, Childs class and location. • 1/3 of deaths from cirrhosis
  • 25.
  • 26.
    26 Outcomes • Torrential bleeding ofvarix! • Acute Bleeding Episodes: < 48 hours – 50 % stop spontaneously – 1 episode → 30 % mortality – Death: aspiration, sepsis, coma, renal failure. • The risk of rebleeding is high (60 to 70 %) until gastroesophageal varices are obliterated. • High Risk Period: < 6 weeks – Rebleeding: 40 – 50 %-in the first 10 days.
  • 27.
    27 Management of EVB Active variceal hemorrhage accounts for about one-third of all deaths related to cirrhosis. • Four major issues related to the prevention and treatment of variceal hemorrhage:  1.Prediction of patients at risk  2.Prophylaxis against a first bleed  3.Treatment of an active bleed  4.Prevention of re-bleeding
  • 28.
    28 PREDICTIVE FACTORS — Clinicaland physiologic factors are useful in predicting the risk of variceal hemorrhage in patients with cirrhosis: • Location of varices • Size of varices: • Appearance of varices • Clinical features of the patient/Child class • Variceal pressure.
  • 29.
    29 Primary prophylaxis • Whatis primary prophylaxis? • How do you prevent VB(primary prophylaxis)?
  • 30.
    30 Primary prophylaxis • Goal: • To reduce portal pressure / intravaricealpressure. – Drugs that reduce portal venous flow or intrahepatic vascularresistance have been used. • Prophylactic propranolol or nadolol therapy is the only cost- effective therapy. • Endoscopic variceal ligation- beneficial for high-risk patients.
  • 31.
    31 Treatment of activebleeding: • There are three primary goals of management during the active bleeding episode: – Hemodynamic resuscitation – Prevention and treatment of complications; and – Treatment of bleeding.
  • 32.
    32 Criteria for ICUAdmission • Institution specific • In general: – Ongoing hemodynamic instability despite IV fluids. – Evidence of active bleeding: hematemesis, large volume bloody lavage, hematochezia – Significant comorbidities: ischemic liver, CAD – Advanced age
  • 33.
    33 Prophylactic antibiotic: • Bacterialinfections ; up to 20% of patients with cirrhosis, hospitalized with UGIB: – The most common sites are : • urinary tract infections (approximately 12 to 29 percent) • spontaneous bacterial peritonitis (7 to 23 percent) • respiratory infections (6 to 10 percent), and • primary bacteremia (4 to 11 percent). – Antibiotics may also reduce the risk of recurrent bleeding.
  • 34.
    34 Management of activebleeding…  Vasopressin:  Terlipressin -a synthetic vasopressin analogue with fewer side effects and a longer half-life than vasopressin and thus can be used in bolus form.  SOMATOSTATIN AND ITS ANALOGS – Syntheticanalogues; octreotide and vapreotid.
  • 35.
    35 ENDOSCOPIC TREATMENT • Endoscopictherapy is currently the definitive treatment of choice for active variceal hemorrhage. • Two forms of endoscopic treatment are commonly used: –Sclerotherapy-best for active bleeding – variceal band ligation
  • 36.
    36 Prevention of rebleeding/recurrentbleeding • What is secondary prophylaxis? • How can you prevent recurrent VB?
  • 37.
    37 Prevention of recurrentbleeding • Over 70 percent of patients experience recurrent variceal hemorrhage within one year of their index bleed. • The risk of rebleeding is greatest immediately after cessation of active bleeding and then declines, reaching close to baseline values by six weeks. • Approximately 70 percent of all untreated patients die within the first year after their initial variceal bleed • Propranolol plus ligation..
  • 38.
    38 Cont… • AASLD GUIDELINES— • The approaches recommended by the guidelines (nonselective beta blockers, endoscopic variceal ligation, transjugular intrahepatic portosystemic shunts, and liver transplantation).
  • 39.
    39 UGIB -PUD  GU/DU There are four major risk factors for bleeding peptic ulcers: – Helicobacter pylori infection – Nonsteroidal antiinflammatory drugs (NSAIDs) – Stress – Gastric acid. • The majority of patients with UGI bleeding due to peptic ulcer disease will stop bleeding spontaneously and most will not rebleed during hospitalization. • Reduction or elimination of these risk factors reduces ulcer recurrence and rebleeding rates.
  • 40.
    40 Summery • Causes ofUGIB • MX of VB • MX of PUD(discussed)
  • 41.
  • 42.

Editor's Notes

  • #14 Upper GI barium studies are contraindicated in the setting of acute upper GI bleeding because they will interfere with subsequent endoscopy, angiography, or surgery 
  • #28  The risk of variceal bleeding correlates independently with the diameter (size) of the varix. The explanation for the relationship between variceal size and bleeding risk is derived from Laplace's law; small increases in the vessel radius result in a large increase in wall tension (which is the force tending to cause variceal rupture).
  • #35 A number of sclerosant solutions are available and one has not been found to be superior to another. The volume and frequency of injections also vary widely. We use 1 to 2 mL of 5 percent sodium morrhuate per injection for a total of 12 to 20 mL per session.