git 4th gib16

50
Dr. Mohamed Alshekhani Professor in Medicine MBChB-CABM-FRCP-EBGH 2016 1 GIB

Upload: shaikhani

Post on 15-Apr-2017

190 views

Category:

Health & Medicine


1 download

TRANSCRIPT

Page 1: GIT 4th GIB16

1

Dr. Mohamed AlshekhaniProfessor in Medicine

MBChB-CABM-FRCP-EBGH2016

GIB

Page 2: GIT 4th GIB16

Introduction:• Upper :80%• Lower :15% • SIB:5%• Proximal or distal to the ligament of Treitz.

Page 3: GIT 4th GIB16

Upper Gastrointestinal Bleeding• Presents with:• Hematemesis (bright-red or “coffee-ground” emesis)• Melena (black, tarry-appearing stool)• Or very rarely hematochezia or bright red blood per rectum due to

briskly UGIB, which is associated with increased mortality.

Page 4: GIT 4th GIB16

UGIB: Causes

• 80% is due to 4 causes: • PUD• EV• Esophagitis• Mallory-Weiss tear.

• Bleeding in 80% stops spontaneously• 20% have persistent or recurrent bleeding, increasing mortality.

Page 5: GIT 4th GIB16

UGIB: Causes• Slow &/or chronic bleeding:• Suggested by history of IDA.• Typical of erosive disease: tumor, esophageal ulcer, portal

hypertensive gastropathy, Cameron lesion (5%, eroded large hiatal hernias)& angiodysplasia.

Page 6: GIT 4th GIB16

UGIB:Causes• Causes of brisk&/or severe upper GIB that increase mortality. • Peptic ulcer• Esophagogastric varices• Dieulafoy lesion• Aortoenteric fistula• Hemobilia: usually from liver or biliary procedural complication or

gallstone complications, tumors &angiodysplasia. • Hemosuccus pancreaticus: (pseudoaneurysm/aneurysm)• Neoplasm• Esophageal lesions• Gastric GIST

Page 7: GIT 4th GIB16

UGIB : evaluation by History• H/O chronic alcohol abuse: a clue to the possibility of VH. • Chronic dyspepsia: PUD.• NSAIDs use: PUD.• H/O Aortic aneurysm repair: aortoenteric fistula.

Page 8: GIT 4th GIB16

UGIB : evaluation by History• Predictors of severe GIB are:• Hematemesis• Comorbidities (such as cirrhosis or malignancy)• HD instability• Hb <8 g/dL (80 g/L). • bleeding source.

Page 9: GIT 4th GIB16

UGIB : evaluation aims• Assessing severity.• Differentiating upper from lower GIB sources. • Determining the need for interventions.

Page 10: GIT 4th GIB16

Evaluation: assessing severity• Outpatient management is usually appropriate when the following

criteria are met: • BUN<18.2 mg/dL (6.5 mmol/L)• Normal Hb• Systolic BP>109 mm Hg• PR< or equal to 100/min• Absence of: melena, Syncope,Liver disease,Cardiac failure.

Page 11: GIT 4th GIB16

Evaluation: assessing severity• Risk-stratification tools guides decisions regarding:• Hospital admission. • Discharge home from ER. • Urgent endoscopy (within 12 hours)• Non-urgent endoscopy (within 24 hours)

Page 12: GIT 4th GIB16

Evaluation: assessing severity• Severity scoring:• Best validated &most useful is Glasgow-Blatchford score (0-23), of 9

variables: BUN (0-6 points), Hb (0-6), SBP(0-3), PR(0-1), melena (0-1), syncope (0-2), hepatic disease (0-2 points)& HF(0-2).

• Has a nearly 100% NPV for severe GIB& the need for hospital-based intervention (blood transfusion, endoscopic therapy, TC arterial embolization, surgery).

• UGIB is most reliably predicted by 4 variables: melena, NGT with blood or “coffee grounds,” BUN/ Cr > 30 & absence of blood clots in the stool.

Page 13: GIT 4th GIB16

UGIB Management:

• 1. Pre-endoscopic care (resuscitation, hemodynamic monitoring, PPI therapy, attention to coagulopathy)

• 2. Early endoscopic evaluation (with excellent endoscopic vision) & treatment.

• 3. Postendoscopic care & risk reduction.

Page 14: GIT 4th GIB16

UGIB Management:• Pre-endoscopic Care:• 1.Resuscitated with crystalloids to reach physiologic endpoints (PR

<100/min, SBP>100 mm Hg&resolution of orthostasis).• 2.Blood transfusion indicated:• A. HD instability &ongoing bleeding or susceptibility to

complications from hypoxia (for example IHD).• B. Target Hb < 7 g/dL, if HD stable with no active or massive

bleeding. • 3.Early (pre-endoscopic) PPI does not improve clinical outcomes

(bleeding, surgery, mortality) but is safe & reduces the likelihood of detecting ulcers with high-risk stigmata & need for endoscopic trt.

• 4.Coagulopathy (INR >1.5) corrected with FRP not vit K (delayed full therapeutic effect) in actively bleeding receiving anticoags.

• 5.Octreotide & antibiotics should be given before endoscopy for suspected variceal bleeding.

Page 15: GIT 4th GIB16

UGIB Management:

• NGT is not required for diagnosis, prognosis, visualization, or therapeutic effect.

• Routine use of prokinetics is not recommended except when patients are suspected of having large amounts of blood in the UGIT; in such cases, erythromycin can be given prior to upper endoscopy.

Page 16: GIT 4th GIB16

UGIB Management:

• Endoscopic treatment:• Upper endoscopy within 24 hours of presentation in patients with

features of UGIB.• Endoscopy within 12 hours is generally recommended only for

patients with suspected variceal bleeding.• Low-risk ulcers not requiring endoscopic intervention are clean-

based or have a non-protuberant pigmented spot.• Intermediate-risk ulcers have adherent clots & should be vigorously

irrigated to dislodge the clot & reclassified based on appearance. • High-risk ulcers that require endoscopic treatment: active arterial

spurting or a non-bleeding visible vessel &.• Routine second-look endoscopy is not required after UGIB unless

rebleeding occurs or the initial examination was incomplete.

Page 17: GIT 4th GIB16
Page 18: GIT 4th GIB16

UGIB Management:

• Post-endoscopic Care & Risk Reduction:• Post endoscopic PPI improves outcome after endoscopic

interventions.• PUD tested for H pylori &If positive, eradication done &confirmed.• If negative, retesting done with an alternative method BZ of false-

negative results with bleeding, PPI, or concomitant antibiotics.• Aspirin should be resumed within 3 - 5 days for patients with

established CVD. • Long-term PPI may not be necessary for aspirin users who undergo

H. pylori testing &eradication.• Long-term, daily PPI should be offered to aspirin users who are H.

pylori negative or those who use concomitant NSAIDs, anticoagulants, glucocorticoids, or other antiplatelets.

Page 19: GIT 4th GIB16

Variceal bleeding Management:

• Octreotide / telipresin infusion & antibiotics are given even if this is suspected.

• FLuid resuscitation is preferred with crystaloids.• Endoscopic intervention can be done safely even with INR up to 2.5

& above that, correction done with FFP.• Endoscopic band ligation is preferred over sclerotherpay for acute

esophageal variceal bleeding.• For bleeding gastric varices cyanoacrylate sclerotherpay is preferred

over band ligation.• When the above measures fail, temponade with esophgeal balloons

as Baltimore-Sengestaken tube is used as bridge to more definitive therapies as TIPS or surgery.

• NS Beta-blockers are used after the control of the bleeding.

Page 20: GIT 4th GIB16
Page 21: GIT 4th GIB16
Page 22: GIT 4th GIB16
Page 23: GIT 4th GIB16

LGIB:

• Typically occurs in elderly.• Presents with hematochezi; acute bright red blood per rectum or

red- or maroon-colored stool. • HD instability is less common but, if present, raises the possibility of

a briskly bleeding UGI source.

Page 24: GIT 4th GIB16

LGIB:

• Causes:• Diverticulosis 30%• Colitis 24%• Ischemic 12%• IBD 9%• Radiation 3%• Hemorrhoids 14%• Postpolypectomy 8%• Colon polyps or cancer 6%• Rectal ulcer 6%• Angiodysplasia 3%• Other 6%.

Page 25: GIT 4th GIB16

LGIB:

• Causes of severe LGIB:• Diverticulosis• Aortoenteric fistula• Colonic or rectal varices• Dieulafoy lesions• Neoplasm• Colitis• Ischemic• IBD• Infectious• Intussusception• Meckel diverticulum• Angiodysplasia

Page 26: GIT 4th GIB16
Page 27: GIT 4th GIB16
Page 28: GIT 4th GIB16

SIB or Obscure GIB

• Relatively uncommon ; 5–10% of GIB. • with advances in SI imaging(VCE, deep enteroscopy& radioimaging)

the cause of bleeding in SI identified in most patients. • OGIB should be reserved for patients in whom a source of bleeding

cannot be identified anywhere in the GI tract. • SIB should be considered in patients with GI bleeding after

performance of a normal upper & lower endoscopic exams. • Second-look exams using upper endoscopy, push enteroscopy&/or

colonoscopy can be performed if indicated before SB evaluation. • VCE should be considered a first-line procedure for SIB& should be

performed before deep enteroscopy if there is no contraindication. • Any method of deep enteroscopy can be used when endoscopic

evaluation& therapy are required.

Page 29: GIT 4th GIB16

SIB or Obscure GIB

• CTE should be performed in patients with suspected obstruction before VCE or after negative VCE exams.

• When there is acute overt hemorrhage in the unstable patient, angiography should be performed emergently.

• In patients with occult hemorrhage or stable patients with active overt bleeding, multiphasic computed tomography should be performed after VCE or CTE to identify the source of bleeding & guide further management.

• If a source of bleeding is identified in the small bowel that is associated with significant ongoing anemia and/or active bleeding, the patient should be managed with endoscopic therapy.

• Conservative management is recommended for patients without a source found after SB investigation, whereas repeat diagnostic investigations are recommended for patients with initial negative SB evaluations & ongoing overt or occult bleeding.

Page 30: GIT 4th GIB16
Page 31: GIT 4th GIB16
Page 32: GIT 4th GIB16
Page 33: GIT 4th GIB16
Page 34: GIT 4th GIB16

BO5:1

• 1.The most common type of GIB is:• Upper.• SIB.• Lower.• Obscure.• None of the above.

Page 35: GIT 4th GIB16

BO5:2

• 2.The least common type of GIB is:• Upper.• SIB.• Lower.• Overt.• None of the above.

Page 36: GIT 4th GIB16

BO5:3

• 3.The most common presentation of UGIB is:• Fresh hematemesis.• Melena.• Hematochesia.• Cofee-ground vomiting.• None of the above.

Page 37: GIT 4th GIB16

BO5:4

• 4.The most common presentation of LGIB is:• Fresh hematemesis.• Melena.• Hematochesia.• Cofee-ground vomiting.• None of the above.

Page 38: GIT 4th GIB16

BO5:5

• 5.The following can be a presentation of UGIB except:

• Fresh hematemesis.• Melena.• Hematochesia.• Cofee-ground vomiting.• None of the above.

Page 39: GIT 4th GIB16

BO5:6

• 6.The following are essential component of significant UGIB except:

• IV access.• PPI.• Upper endoscopy.• NG Tube.• Blood grouping and cross match.

Page 40: GIT 4th GIB16

BO5:7

• 7.The prokinetic of choice in severe upper GIB is:

• IV metochlorpromide.• IV erythromycin.• Oral erythromycin.• Oral domperidone.• None of the above.

Page 41: GIT 4th GIB16

BO5:8

• 8.Interventions that improve survival in severe upper GIB include all except:

• Endoscopic hemostasis if indicated.• Pre-endoscopy PPI.• Post-endoscopic PPI.• Radiological intervention.• Surgery.

Page 42: GIT 4th GIB16

BO5:9

• 9.The need for endoscopic intervention is decided by:

• Forrest classification.• Blackford scoring.• Glasgo scoring.• Apgar scoring.• Non of the above.

Page 43: GIT 4th GIB16

BO5:10

• 10.The following endoscopic lesions warrants endoscopic intervention during UGIB except:

• Spurting vessel.• Oozing lesion.• Visible vessel.• Adherent clot.• Ulcer with pigmentation.

Page 44: GIT 4th GIB16

BO5:11

• 11.The endoscopic intervention of choice for severe UGIB is:

• Single.• Dual.• Triple.• All.• None.

Page 45: GIT 4th GIB16

BO5:12

• 12.H Pylori testing during UGIB is frequently:• False positive.• False negative.• Accurate.• Need need not to be repeated.• All of the above.

Page 46: GIT 4th GIB16

BO5:13

• 13.The first step in managing severe LGIB is:• Colonoscopy.• Exclude upper GI source.• Surgery.• IV PPI.• All of the above.

Page 47: GIT 4th GIB16

BO5:14

• 14.The best approach in managing severe LGIB which can not be hemoynamicly be stabilized is:

• Angiographic intervention.• Colonoscopy.• Surgery.• IV PPI.• All of the above.

Page 48: GIT 4th GIB16

BO5:15

• 15.Endoscopy in non-variceal UGIB is indicated within:

• 12 hours.• 24 hours.• 36 hours.• 48 hours.• 72 hours.

Page 49: GIT 4th GIB16

BO5:16

• 16.Endoscopy in variceal UGIB is indicated within:

• 12 hours.• 24 hours.• 36 hours.• 48 hours.• 72 hours.

Page 50: GIT 4th GIB16

BO5:17

• 17.The following should be given in suspected variceal UGIB except:

• Somatostatin.• Telepressin.• PPI.• Antibiotics.• Crystaloides.