CDEM curriculum part 2 Flashcards

1
Q

How to classify an upper GI bleed vs lower GI bleed

A

Ligament of Treitz is the dividing line and crosses the small intestine at the duodenal-jejunal junction

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2
Q

Initial actions and primary survey of GI bleed

A

Adequacy of the airway, breathing and circulation must be the initial concern for any pt with acute GI bleed and/or hemodynamic instability
Some pts may require intubation
IV access should be obtained during your initial eval of the pt
Minimum of 2 large-bore IVs should be placed
If not possible, a trauma line or cordis should be considered
If acutely unstable, consider transfusing un-crossmatched blood and IVF while a type and cross-match is being performed

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3
Q

Esophageal tamponade- when should it be considered?

A

Severe UGIB that cannot be controlled
Unstable vital signs
No ability for emergent endoscopy

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4
Q

Lab eval of GI bleed

A
CBC
Chemistry
PT
PTT
Type and cross
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5
Q

Primary indication for blood transfusion in GI bleed

A

Hemorrhagic shock despite IVF resuscitation
Pts with subacute bleeding and hemsoglobin of 7 or symptomatic anemia at a hgb of 8 or 9
Hbg concentration always needs to be viewed in context to the clinical condition of the pt

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6
Q

Indications to consider immediate transfusion in GI bleed

A

Massive upper or lower GI bleed
Hemoglobin dropping at a rate 3 g/dL over 2-4 hrs in the setting of active bleeding
Hemoglobin <9 in the setting of active bleeding
Anemia induced end-organ injury

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7
Q

Anticoagulation with GI bleed

A

Risks and benefits of reversal should be weighed

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8
Q

Location of GI bleeding- how to determine

A

Pt hx:
Hematemesis or coffee ground emesis- upper GI bleed
Melena
Hematochezia- LGIB or UGIB with significant bleeding and increased GI motility

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9
Q

When can an NG tube be placed in GI bleeding?

A

If a pt has intractable emesis or if there is still a question about if the pt has an upper GI bleed

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10
Q

When should a bleeding scan be considered in a GI bleed?

A

Pts with moderate lower GI bleeding (stable VS with or without administration of blood products)
Can be useful in a pt with a recurrent GI bleed, with a negative colonoscopy and endoscopy in the past for similar bleeding episode

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11
Q

Pharmacologic therapy for GI bleed

A

PPIs are first line for acid suppression in pts with upper GI bleed
H2 blockers are often second line and used to reduce acid production in an outpt setting as a PO med
Somatostatins for pts with known or highly suspected variceal bleeding
Abx for a pt with a GI bleed who has a hx of cirrhosis

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12
Q

Dispo in GI bleed: mild

A

Pts with a mild GI bleed can be d/c-ed:
In general, no more than a mild anemia, no active bleeding besides a pos stool guaiac or blood-streaked emesis
They need prompt f/u

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13
Q

Dispo in GI bleed: more severe or acute GI bleed

A

Admission

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14
Q

Decision for floor vs ICU for severe GI bleed that requires admission

A
Unstable vital signs
Rate of bleeding
Need for blood transfusion
Potential for decompensation
Comorbidities
Need for procedures/sedation only avaialble in the ICU or OR
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15
Q

DDx of UGIB

A
Gastric ulcer
Duodenal ulcer
Gastritis
Esophagitis
Gastroesophageal varices
Mallory-Weiss tear
Aortoenteric fistula
Malignancy
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16
Q

DDx of LGIB

A
Diverticulosis
Meckels diverticulum
Angiodysplasia
Malignancy
Colitis (d/t infection, ischemia, IBD)
Anorectal (hemorrhoids, fissures)
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17
Q

Description of shock

A

A physiologic state where oxygen delivery to the tissues is inadequate to meet metabolic requirements, causing global hypoperfusion

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18
Q

How can shock be described?

A

Compensated (nl BP with inadequate perfusion) or uncompensated (hypotension and inability to maintain nl perfusion)

19
Q

Hypovolemic shock physiology

A

Decreased circulatory volume

20
Q

Hypovolemic shock examples

A

Hemorrhage or fluid loss

21
Q

Cardiogenic shock physiology

A

Impacted heart pump function

22
Q

Cardiogenic shock examples

A

ACS
Valve failure
Dysrhythmias

23
Q

Distributive shock physiology

A

Pathologic peripheral blood vessel vasodilation

24
Q

Distributive shock examples

A

Sepsis
Anaphylaxis
Neurogenic

25
Q

Obstructive shock physiology

A

Non-cardiac obstruction to blood flow

26
Q

Obstructive shock examples

A

PE
Tension pneumo
Tamponade

27
Q

Classic presentation hx of shock

A

Obvious bleeding from trauma or an anatomic source (GI, vaginal, or ENT) suggests hypovolemic shock, as does decreased PO intake or fluid loss d/t vomiting, diarrhea, excess urination or otherconduit (ostomy)
CP, SOB, leg swelling, or syncope may precede the development of shock d/t a cardiac (ACS, CHF) or obstructive PE cause
Sudden onset of hives, face or body swelling whether associated with a known trigger or not can signal anaphylactic (distributive) shock
Signs of infection such as fever with cough, abdominal pain, or HA may indicate sepsis
In some cases, however, non-focal, vague sx such as weakness, altered mental status, or malaise may be the only presenting signs of any of the types of shock

28
Q

PE of shock

A

Findings are also variable

BP alone should not be used as the sole marker to determine shock

29
Q

Presentation of early shock

A

May present with nl or even elevated BP and nl HR, but if left untreated, tachycardia and hypotension will follow

30
Q

Presentation of hypoperfused pts in shock

A

Often exhibit cool, pale, or cyanotic skin with: Decreased cap refill and dry mucous membranes
Confusion, altered mental status or coma
Thready pulses or tachypnea

31
Q

Presentation of cardiogenic shock

A

Arrhythmias, JVD, and dependent edema may be present

32
Q

Shock index

A

Heart rate divided by SBP
Can provide clues to the severity of the pt’s condition
Nl index ranges from 0.5-0.7
Repeated values >1.0 indicate decreased LV function and are associated with higher mortality

33
Q

Tests to be considered for shock

A

CBC and coag studies (to determine anemia/blood loss, infection, hypocoagulability)
Electrolytes
BUN/creatinine and UA; hepatic function panel (to assess liver and renal function)
CXR, EKG
Lactate (to gauge the degree of hypoperfusion)
Urine pregnancy test
More invasive testing is often required:
-ABG for O2/pH
-Central venous oxygen measurement, SVR, and CO may be measured through special central venous catheters

34
Q

Further studies in shock

A
Infectious etiology (sepsis)- blood, sputum, urine, pelvic, or wound cultures, head CT and LP, targeted imaging (US/CT)
Cardiogenic- cardiac enzymes and echo
Obstructive- CT or V/Q scan (PE), echo (tamponade)
35
Q

How do I make the dx of shock?

A

Should be strongly considered in ill-appearing pts with: -VS abnormalities (particularly tachycardia and hypotension)
-Altered mental status
-Signs of organ hypoperfusion
In most cases, the clinical picture should guide decision making

36
Q

Cardiogenic shock: HR, CVP, contractility, SVR

A

HR increased
CVP increased
Contractility sig decreased
SVR increased

37
Q

Hypovolemic shock: HR, CVP, contractility, SVR

A

HR increased
CVP sig decreased
+/- increased in contractility
SVR increased

38
Q

Distributive shock: HR, CVP, contractility, SVR

A

Increased HR
CVP sig decreased
+/- contractility
SVR decreased

39
Q

Obstrutive shock: HR, CVP, contractility, SVR

A
Increased HR
\+/- increased CVP
\+/- contractility
Increased SVR in tamponade, PE
Decreased SVR in tension pneumo
40
Q

Common lab results in shock

A

Anemia, disorders of platelets or coagulation studies
Elevated or depressed WBC with left shift
Elevated lactate level or decreased serum bicarb (suggests a shift to anaerobic metabolism and tissue hypoperfusion)
Evidence of end-organ damage: elevated creatinine, abnl LFTs, ARDS/edema on CXR, arrhythmia/ischemia on EKG or abnl cardiac enzymes, ischemic neurologic changes on CT/MRI

41
Q

Tx of shock

A

Should begin emergently
Start with the ABCs
-Intubation should be strongly considered
–Keep in mind that many drugs used in intubation, as well as pos pressure ventilation, can have neg hemodynamic effects
-Obtain IV access through large bore peripheral lines or a central venous catheter
Crystalloid fluids should be given as boluses
-Be careful with rapid fluid administration to the pt in cardiogenic shock with pulm edema
If volume resuscitation does not improve hemodynamic status, vasoactive meds may be used

42
Q

Tx of shock: when aggressive tx of the underlying cause of shock is warranted

A

Hypovolemia d/t hemorrhage may warrant surgical or interventional control
Sepsis syndromes should be treated with early goal-directed therapy (maximization of oxygen delivery, careful hemodynamic monitoring) and aggressive antibiotic tx
Cardiogenic shock may necessitate emergent angiography or surgical procedures (bypass, valve repair, IABP)
Obstructive shock d/t PE often requires anticoagulation or thrombolysis, whereas when d/t cardiac tamponade emergent drainage of the pericardial fluid may be necessary

43
Q

Tx of shock: monitoring

A

Using a urinary catheter, intraarterial BP measurement and central venous pressure monitoring

44
Q

When is resuscitation of a shock state successful?

A

Normalization of hemodynamic state (BP, HR, and urine output)
Lactate decreases by half in the first couple of hours
Nl volume status restored
Maximal tissue oxygenation
Resolution of acidosis and return to nl metabolic parameters