Heme/Onc Flashcards

1
Q

Definition of anemia in the newborn

A

< 13

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2
Q

Normal RBC MCV

A
  • Newborns normal up to 110
  • 6 months - 2 years = 70-90 note lower than normal in children and adults
  • Older children and adults = 80-100
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3
Q

Definition of polycythemia

A
  • Hct >65%

- Treatment required only >70%

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4
Q

Problems associated with polycythemia

A
  • Hypoglycemia
  • Thrombocytopenia
  • Joint pain
  • Clotting
  • Stroke
  • Hempotysis
  • Lethargy
  • Hypotonia
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5
Q

Risk factor for polycythemia

A
  • IUGR
  • Delayed cord clamping
  • Twin-twin transfusion
  • IDM
  • Down Syndrome
  • Chronic hypoxia
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6
Q

Treatment for polycythemia

A

Partial volume exchange transfusion

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7
Q

Complications of pRBC transfusion

A
  • HYPOcalcemia
  • HYPERkalemia
  • Thromcobytopenia
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8
Q

Laboratory findings in iron deficiency anemia

A
  • Microcytic anemia
  • Low transferrin saturation
  • High RDW
  • Low reticulocyte count
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9
Q

Causes of basophilic stippling

A
  • Beta Thalassemia Major

- Lead toxicity

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10
Q

Vitamin K Dependent Factors

A
  • 2, 7, 9 and 10

- Part of intrinsic pathway of coagulation cascade

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11
Q

Bernard-Soulier Syndrome

A
  • Mild thrombocytopenia
  • LARGE platelets
  • Prolonged bleeding time
  • Platelets are LARGE like a St. BERNARD*
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12
Q

Glanzmann thrombasthenia

A
  • Dysfunctional platelets
  • NORMAL platelet count, PTT and INR
  • Possible presentation: unexplained bleeding in patient with above normal labs*
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13
Q

ITP

A
  • Often occurs after viral syndrome
  • LARGE platelets (think of plts being released early, when they are larger, due to immune plt destruction)
  • Tx with IVIG (preferred), steroids and possible RhoGAM (if Rh+ - to cause mild hemolysis and “distract” immune system)
  • Important to RULE-OUT leukemia before treating with steroids!
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14
Q

Main factors in extrinsic coagulation pathway

A
  • III and VII
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15
Q

What part of coagulation cascade is Factor X a part of?

A

Common pathway

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16
Q

Vitamin deficiency that results in high PT/INR

A

Vitamin K deficiency

17
Q

Wiskott-Aldrich Syndrom

A
  • X-linked (only occurs in males)
  • Thrombocytopenia, eczema, frequent infections
  • Platelets small in size and/or number
  • IgM low, IgA high
  • Increased risk of lymphoma in 30s
  • Cure with BMT
18
Q

Kasabach-Merritt Syndrome

A
  • Large, congenital vascular tumors
  • No true hemangiomas
  • May result in severe CONSUMPTIVE coagulopathy
  • Most common in infants
19
Q

What lab abnormality is seen with vitamin K deficiency?

A

High PT/INR

20
Q

What lab abnormality is seen with Hemophilia A or B?

21
Q

Factor deficiency in Hemophilia A

A
  • Factor VIII deficiency

* A sounds like 8*

22
Q

Factor deficiency in Hemophilia B

A
  • Factor IX deficiency

* A sounds like 8; B comes after A and 9 comes after 8*

23
Q

What maternal medications may cause bleeding in infant?

A
  • Antibiotics
  • Seizure medications
  • Warfarn
24
Q

vonWillebrand Disease

A
  • Deficiency of vonWillebrand factor
  • Factor VIII and platelets depend on vWF
  • Elevated PTT and bleeding time
  • Dx = measured factors VIII and IX (to R/O hemophilia) and vWF (to confirm that level is low)
25
Treatment of vWD
- Minor bleeding = no treatment OR DDAVP - Severe bleeding = Factor VIII concentrate (Hamate P), cryoprecipitate (has fibrinogen, VIII and vWF) - May give aminocaproic acid for mucosal bleeds (inhibits fibrinolysis)
26
DIC laboratory findings
- Thrombocytopenia - Low fibrinogen - Elevated fibrinogen split products (D-Dimer) - Elevated thrombin time, PT and PTT
27
Treatment for DIC
- Give platelets and pRBCs - Give CRYOPRECIPITATE for low fibrinogen (cryoprecipitate includes fibrinogen, factor VIII and vWF) - Low clotting factors -> treat with FFP (has most clotting factors) - Treat underlying condition (i.e. burns, malignancy, pregnancy, sepsis)
28
Encapsulated organisms
* Some Nasty Killers Have Some Capsular Protection* - S. pneumo - N. meningitides - Klebsiella pneumoniae - H. influenzae - Salmonella - Cryptococcus - Pseudomonas
29
What does bleeding time measure?
Platelet adherence to injured capillaries as well as platelet activation and aggregation
30
What does PTT evaluate?
Presence and function of factors in coagulation cascade
31
What does PT evaluate?
- Function of factors in intrinsic pathway in coagulation cascade - Prolonged with vitamin K deficiency because factors 2, 7, 9 and 10 are the vitamin K dependent factors and are part of intrinsic pathway
32
What are Heinz bodies?
- Denatured hemoglobin | - Present with G6PD deficiency, alpha thalassemia
33
What findings are noted on blood smear with beta thalassemia major?
- Target cells | - Basophilic stippling