Anemia and Coagulopathy Flashcards

1
Q

CaO2 formula

A
CaO2=(Hgb x 1.39)SaO2 + PaO2(0.003)
1.39 = O2 bound to hemoglobin
SaO2= saturation of hemoglobin with O2
PaO2= arterial partial pressure of oxygen
0.003 = dissolved oxygen ml/mmHg/dl
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2
Q

Compensatory mechanisms for anemia

A

Increased cardiac output
Increased red blood cell 2,3-diphoshoglycerate (DPG)
Increased P-50
Increased plasma volume
Decreased blood viscosity
Decreased SVR
RIGHTWARD shift of Oxygen-Hemoglobin dissociation curve
Redistribution of blood flow to organs with higher extraction ratio (ER)

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3
Q

Changes that could interfere with oxygen delivery to tissues

A

Decreased cardiac output
LEFTWARD shift of Oxygen-Hemoglobin dissociation curve
Resp alkalosis (hyperventilation/ decreased PaCO2)
Hypothermia
Abnormal Hgb (including fetal Hgb and carboxyhemoglobin)

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4
Q

Anemia: basic anesthetic management

A

Know your patient’s preoperative
hemoglobin (Hgb)
hematocrit (Hct)
Anemia is suspected if hemoglobin

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5
Q

Chronic anemia anesthetic management

A
  1. Maximize O2 delivery
    Consider ↑ FiO2
  2. Avoid drug-induced ↓ in C.O.
    Selection of induction agent (etomidate)
    Anesthetic technique (↑ opioid)
    Hydrate, if tolerated; avoid hypovolemia
  3. Avoid conditions that favor a leftward shift of the oxyhemoglobin dissociation curve
    Avoid hyperventilation/ respiratory alkalosis
    Avoid hypothermia
  4. Volatile anesthetics
    May be less soluble in plasma of anemic patient
    May need less inhaled anesthetics for effect
    Consider that this decrease in solubility may be offset by the impact of increased cardiac output
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6
Q

Goal of transfusion therapy

A

Goal of transfusion therapy
to increase oxygen-carrying capacity
correct a coagulation disorder

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7
Q

S/S of B12 deficiency anemia and anesthetic considerations:

A

B-12 deficiency may result in pernicious anemia
Bilateral peripheral neuropathy
Loss of proprioceptive and vibratory sensations in lower extremities
Decreased deep tendon reflexes
Unsteady gait
Memory impairment and mental depression

Anesthesia:
Avoid regional blocks due to neuropathies
Avoid nitrous oxide
Maintain oxygenation
Emergency correction for imminent surgery is with red cell blood transfusions

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8
Q

Folic acid deficiency anemia s/s and anesthetic considerations

A
Folic acid deficiency may result in pernicious anemia 
Smooth tongue
Hyperpigmentation
Mental depression
Peripheral edema
Liver dysfunction
Severely ill patients

Oral manifestations may make airway management challenging (changes in tongue texture, etc.)
Have an alternate airway management plan!

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9
Q

What are some hemolytic anemias and their anesthetic considerations?

A

Hereditary spherocytosis:
Paroxysmal nocturnal hemoglobinuria
Glucose-6-Phosphate Dehydrogenase: Acute and chronic episodes of anemia
Need to avoid exposure to oxidative drugs
Avoid hypothermia, acidosis, hyperglycemia, infection

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10
Q

Perioperative risks and concerns of hemolytic anemia

A

Perioperative risks and concerns
↑ risk of tissue hypoxia
If previous splenectomy may have ↑ risk of perioperative infection
Increased risk venous thrombosis due to activation of coagulation
Erythopoietin is often prescribed for 3 days preoperatively
Acute drops in Hb below

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11
Q

Sickle cell disease avoid all situations leading to?

A

Hypoxemia
Hypovolemia
Stasis

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12
Q

Perioperative risks and concerns

A

Look for evidence of organ damage, cardiac dysfunction, concurrent infection
May benefit from conservative transfusions with high risk surgery
ASA recommends pre-operative transfusion to increase HCT to 30%
Goal of transfusion is to decrease Hgb S to less than 30%
Supplemental O2
Preoperative hydration for 12 hours prior to surgery
Pre-med
avoid respiratory depression leads to acidosis
Regional anesthesia is advocated
concern with hypotension
stasis of blood flow
compensatory vasoconstriction
Aggressive pain management
Avoid infections
Avoid tourniquets

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13
Q

What is acute chest syndrome and its treatment?

A

Acute chest syndrome-can be fatal (typically 2-3 days postop)
Pleuritic chest pain, dyspnea, fever, acute pulmonary hypertension
Transfusion or exchange transfusion to hct of 30%
Supplemental 02
Antibiotics
Inhaled bronchodilators
Aggressive pain management

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14
Q

Thalassemia perioperative risks and concerns

A

CHF common with severe anemia
Cardiac arrhythmias due to heart failure
Hemodynamic compromise with induction agents if low cardiac reserve-use cardiac sparing drugs
Very sensitive to the effects of digitalis
Hepatosplenomegaly
Coagulopathy (? Regional Anesthesia)
Hypersplenism can result in thrombocytopenia and ↑ risk of infection
Potential difficult airway 2° to maxillary deformities
Consider awake fiberoptic intubation
Complications of iron loading from chronic therapy
Diabetes (Blood glucose monitoring)
Adrenal insufficiency (↓ response to vasopressors)
Liver dysfunction & Coagulation abnormalities
Hypothyroidism & hypoparathyroidism
Arrhythmias (ECG)
Right-sided Heart failure (ECHO)

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15
Q

What is thalassemia major and minor?

A
Thalassemia major
Inability to form beta-globin chains of hemoglobin 
Hepatosplenomegaly
Dypnea and orthopnea
Infection risk
Arrhythmias , CHF
Skeletal malformations
Growth failure
Hemothorax 
Spinal cord compression
Mental retardation
Very sensitive to digitalis
Increased RBC production
Jaundice

Minor:
Heterozygous state (trait)
Mild anemia
Normal RBC count

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16
Q

What is aplastic anemia?

A

Aplastic anemia refers to bone marrow failure characterized by destruction of rapidly growing cells
caused by drugs, radiation or infectious processes

17
Q

Aplastic anemia risk and concerns

A

Patients on immunosuppressive therapy
Steroid “stress” dose should be considered
Reverse isolation due to thrombocytopenia and increased risk of infection
Prophylactic antibiotics due to neutropenia
Hemorrhage (GI & Intracranial)
LV dysfunction 2° high output state and fluid overload
Co-existing congenital abnormalities
Fanconi anemia is the peds version
Cleft palate; cardiac defects
Difficulty cross-matching blood products after multiple transfusions

18
Q

Aplastic anemia induction, maintenance, and extubation concerns?

A
1. Preinduction/induction
Consider transfusions before induction
Airway hemorrhage possible with DVL 
Avoid nasal intubation 
Regional Anesthesia 
Labile hemodynamic response to induction
2. Maintenance
PEEP will facilitate use of ↓ FiO2
Avoid nitrous oxide 
Maintain normothermia
3. Extubation and postoperative period
Period with greatest O2 demands
Monitor coagulation status
19
Q

What is Methglobinemia?

A

Methemoglobin is formed when iron moiety in Hgb is oxidized from the ferrous (Fe2+) state to the ferric (Fe3+) state
Methemoglobin is a markedly left-shifted Hemoglobin that, due to its higher oxygen affinity, delivers little oxygen to the tissues
Normal level is 1%
At levels between 30% and 50%, -patients begin to exhibit symptoms of oxygen deprivation, blood is brown
from Nitrate poisoning, or local anesthetics: prilocaine

20
Q

Anesthetic considerations

A

Can influence the accuracy of pulse oximetry as methhemoglobin absorps light equally in both red and infrared.
At Sa02 of >85% underestimates the true value
At Sa02 of

21
Q

Clinical signs associated Acute Blood loss (20%EBV)

A

Tachycardia
Orthostatic hypotension
CVP change

22
Q

Clinical signs associated Acute Blood loss (40%EBV)

A
Tachycardia
Hypotension
Tachypnea
Oliguria
Acidosis
Restlessness 
Diaphoresis
23
Q

Blood loss treatment?

A

Monitoring:
Invasive monitoring? (CVP, Arterial BP, +/- PA)
UOP - ? hematuria
Induction:
Ketamine/Etomidate
Maintenance:
May be unable to tolerate even modest levels of volatile anesthetics
Scopolamine, benzodiazepines, and opioids
Use vasopressors sparingly
Keep warm
Watch surgical field for non-clotting blood
Post-operative:
May require postoperative ventilation due to anticipated fluid shifts from resuscitation
Pulmonary edema
ARDS

24
Q

Define massive transfusion and its considerations?

A

Defined as:
Transfusion of > 10 units of RBC in 24 hour period
Replacement of atleast one blood volume in 24 hour period
Replacement of 50% blood volume in 6 hour period
Associated with several consequences due to property of blood, agents to preserve blood and storage, tissue hypoperfusion
Hypothermia
Volume overload
Dilutional coagulapathy
Decreased in 2,3 diphosphoglycerate
Hyperkalemia
Citrate toxicity (binds calcium)

25
Q

Describe polycythemia

A
Expanded red cell mass and increased Hct
Caused by:
Reduction in plasma volume (dehydration)
Production of excess RBC (polycythemia vera)
Chronic hypoxia
Increased blood viscosity
Venous / arterial thrombosis leading to CAD, pulm HTN, CNS disorders
Usually minor, until Hct > 55%
26
Q

Describe Hemophillia A

A
Congenital factor VIII deficiency 
Severe Hemophilia:
Factor VIII levels less than 1% of normal 
Diagnosis as children due to frequent spontaneous  hemorrhages in joints and muscles or organs  
Moderate Hemophilia:
Factor VIII levels 1% to 5% of normal 
Reduced severity of the disease 
Increased risk bleeding with surgery
Less problems with joints and muscles
Mild Hemophilia:
Factor VIII levels as low as 6% to 30% 
often undiagnosed until adulthood
Increased bleeding risk with major surgery
Significantly prolonged PTT /normal PT
27
Q

Hemophillia A anesthetic considerations

A

Anesthesia Considerations :
factor VIII level must be brought to near normal (100%) for surgical procedure
Infusion of factor VIII concentrate
initial infusion of 50 to 60 U/kg

28
Q

Describe hemophillia B

A
Congenital factor IX deficiency
Severe disease
Factor IX levels of less than 1% 
Associated with severe bleeding
Moderate disease
Factor IX levels of  bleeding 1% to 5%
Mild disease
Factor IX levels of between 5% and 40% 
Significantly prolonged PTT /normal PT
29
Q

Hemophillia B anesthetic considerations

A

Anesthesia Considerations :
100 U/kg
recombinant/purified product or factor IX–PCC are used to treat mild bleeding episodes or as prophylaxis with minor procedures
At risk for thromboembolic events

30
Q

Describe von Willebrand’s disease

A

Disorder of platelet function
Platelet count normal
Bleeding time is markedly prolonged (normal is 3-10minutes)
May have prolonged PTT

31
Q

Anesthetic considerations for von Willebrand’s disease

A
Anesthesia Considerations:
Avoid nasal intubations or insertion of nasal trumpets
DDAVP therapy (Desmopressin) –mild bleeding or minor surgery

Cryoprecipitate – more reliable for severe bleeding or surgical prophylaxis
Cryoprecipitate is a readily available and effective blood product that contains concentrated fibrinogen, vWF, and factors VIII and XIII

32
Q

Drugs that induce platelet dysfunction

A
  1. ASA (NSAIDS) administration irreversibly inhibits cyclooxygenase which is necessary for platelet aggregation
    Bleeding Time is prolonged 2-3 minutes within 3 hours of ASA ingestion
    Lasts the lifetime of platelet
    Bleeding time returns to normal within 72 hours but aggregation may not return for normal for 7-10 days
  2. Antibiotics
    Interfer with platelet adhesion and activation
    Biggest impact on critically ill patients
  3. Volume expanders

Hypothermia (

33
Q

Describe thrombocytopenia

A

Low platelet count
Normal platelet count 150,000-450,000
Approximately 1/3 platelets are sequestered in the spleen
Signs include petechial rash, bleeding from nose, GI tract, bruising
Platelet count >50,000 needed for major surgery to control bleeding
Each unit of apheresis platelets or six units of random donor platelets (six pack) should increase platelet count approx 50,000