Heme Flashcards

1
Q

Heme hx questions

A
blood disorders
bruise easy
bleeding/clotting problem
prolonged bleeing, nose, gums
blood tranfusion
family hx of blood disease 
Meds/herbs: ASA, vitE, ginseng, garlic
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2
Q

what concerns you with physiology of heme

A

dec O2 carrying capacity

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3
Q

O2 dissociation curve R and L

A

R: release, Inc: temp, 2,3dpg, anemia, dec: pH
-so avoid hypervent, and keep warm
L: Love DEC temp, 2,3dpg, INC: pH

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4
Q

Chronic anemia compensation

A

Better than acute bc of Compensation
dec SVR to improve O2 delivery
Inc CO and plasma volume
Blood flow to organs with higher O2 need–brain, heart

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5
Q

Anemia asmt

A

Shift to the right
H&H in context with fluid status? hemoconcentrated?
W

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6
Q

Goal of transfusion

A

will it improve their O2 carry capacity? or correct coag disorder
**based on will this improve their O2 capacity and prevent the consumption from exceeding the delivery
only give if necessary

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7
Q

Anemia of chronic disease

A

2nd to something else
dont disrupt compensatory mechanisms
Inc CO needed to maintain O2 delivery

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8
Q

Acute blood loss

A

takes 3 days to reach new plateau…can take a while to see changes
need VOLUME have “pressures” aka catecholamines

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9
Q

Hemolytic anemia

A

inc risk of tissue hypoxia
splenectomy-inc risk of infx
*EPO rx for 3days prior to OR
consider transfusion at

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10
Q

Sickle cell dz

A
Right shift 
anemia is well tolerated
Keep warm
well hydrated 12hrs prior to surg
ECG (infarction) 
Exercise tolerance
When premed-- avoid resp depression or get acidosis 
**conservative transfusion at 10 for high risk surg
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11
Q

Sickle cell crisis

A

Life-threatening
take measure to avoid vaso-occlusive
*Hydration, Oxygen, Warm, no stasis
Pain meds

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12
Q

Thalassemia

A

CHF
difficult airway: facial deformities,
complications from iron loading from chronic transfusion:
DM, Adrenal insufficiency– get a dec response to pressures, Coag problems, Hypothyroid and hypoparathyroid, Arrhythmias, Liver dysfunction
**ECG, Elytes, LFT Coag–regional??
Monitor: invasive? HF

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13
Q

Aplastic anemia

A
LV dysfunction (due to high output status)
Severe Congenital heart dz
Dec: Plt, RBC, neutrophil 
*CBC, may need pre op transfusion 
*risk for airway hemorrhage 
*reverse isolation
*prophylactic abx
*stress steroid dose
*Invasive monitoring 
*avoid  nasal intubation 
*labile hemodynamic responce to induction 
*regional --depends on coags
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14
Q

Prophyria

A

errors in metabolism- Overproduction of prophyrins

Attack symptoms: PAC WAG: abd pain, GI disturbances, ANS instability, CNS disturbance Life threatening muscle weakness

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15
Q

Unsafe meds for Prophyria

A

BED SPANK
Barbs
Etomidate
Diazepam

Sulfonamide abx
Phenytonin
Alcohol 
Nifedipine
Ketorolac
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16
Q

Hemophilia A

A
def clotting factor 8, abn PTT 
tx: factor 8 and desmopressin
17
Q

Hemophilia B

A

problem clotting factor 9, abn PTT

tx: factor 9

18
Q

Von Willebrands

A

problem with vWF and 8, Inc Bleeding time

tx: cryo and desmopressin

19
Q

Minimum acceptable hgb and hct

A
Duration-acute/chronic
Etiology
IV fluid status 
Urgency of surgery
Anticipated blood loos in surg 
Co-existing dz