Anemia and Bleeding Flashcards

1
Q

What History or questions with anemia

A
  • Duration of symptoms?- Chronic vs acute
  • Episodic?- Drug or illness driven?
  • Associated symptoms?
  • Jaundice/dark urine= hyperbili=hemolysis
  • Medications
  • Iron source in diet?
  • Family Hx- early gallstones, food intolerance, etc.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Review of symptoms in anemia

A
  • Feeding?
  • Bruising/bleeding
  • Rashes
  • Joint/Bone pain
  • Fevers
  • Other symptoms: viral syndromes in past couple weeks
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

PE in anemia pt

A
  • CV: Tachycardia, murmur, CHF (feeding problems)
  • Lungs: Crackles, wheezes
  • Liver/spleen enlargement
  • Ascites/edema
  • Pallor (palmar creases-lighter color)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Lab eval in anemia

A
  • Basic workup: CBC, Peripheral smear, retic count. Bilirubin, DAT (Coombs Test), UA
  • Focused workup: Depends on Hx/PE. Includes iron studies, osmotic fragility, Hgb electrophoresis, G-6PD
  • Retic: gauge RBC production rate
  • RDW: Gauge homogeneity of RBC population.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Cell size normocytic, retic increased. Likely Dx?

A

1) Blood loss
2) Hemolysis
3) AIHA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Cell size normocytic, decreased retic. Likely Dx

A

-Anemia of chronic disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Cell size macro, increased retic. Likely DX?

A
  • Blood loss

- Hemolysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Cell size Macro, retic decreased. Likely Dx?

A
  • Folate/B12 def.
  • Drug induced
  • Marrow failure
  • AIHA
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Cell size micro, retic decrease. Likely Dx?

A
  • Iron def.

- AIHA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Cell size micro, retic increased. Likely dx?

A
  • Thalassemia

- AIHA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Iron deficiency anemia would look like what under microscope?

A

-Microcytic, hypochromic aregenerative anemia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Leading cause of anemia in Children? And leading cause of MR and LD in children?

A

Iron deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Pathophys of Iron deficiency? (3)

A

1) Inadequate dietary intake
2) Excessive consumption (growth spurt)
3) Excessive loss (GI blood loss, menses, pulm bleeding, excessive sports in children/teens)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Treatment of Iron deficiency

A
  • Find site of blood loss.
  • Iron replacement- Ferrous sulfate 3-6 mg Elemental Iron/Kg/day TID- Retic increase in 3-5 days, Hgb increases 0.25 grams/dl per week, treat 4-6 months. Replace BM stores and stores elsewhere.
  • Patients with Chron’s or other problems that dont respond to Ferrous sulfate can be given IV iron
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is this: Clinical syndrome where there is just about enough iron to make a normal Hgb, but no reserve. Common in teen girls (diet restriction, menstrual loss, exercise). What can this cause in pregnancy?

A
Non Anemia (latent) iron deficiency
-Iron deficient babies- neurologic problems, lasting behavioral and intellectual defects.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

The most common form of anemia in adults. Second most common in childhood. Seen with common infection. Stimulation of inflammatory processes.

A

Anemia of Chronic Dosorders

17
Q

What does Anemia of Chronic disorders look like under mcroscope

A

Normocytic/Normochromic anemia

18
Q

Anemia of Chronic disorders lab features

A
  • Transferrin low
  • Serum iron low
  • Serum transferrin receptor low
  • TIBC low
19
Q

Bleeding disorders come from three sources. Match number with letter:

1) Vascular phase
2) Platelet Phase
3) Humoral phase

A) Thrombocytopenia, VWD
B) Ehlers-Danlos Syndrome
C) Hemophilia, DIC

A

1-B
2-A
3-C

20
Q

Each phase has a pattern of bleeding:

1) Humoral:
2) Vasc/Platelet

A

1) Bleeding into soft-tissue/joints

2) Muco-cutaneous bleeding

21
Q

Bruises age and change color. How old is a…

1) Red (swollen tender)
2) Blue
3) Green
4) Yellow
5) Brown
6) Clear

A

1) 0-2 days
2) 2-5 days
3) 5-7 days
4) 7-10 days
5) 10-14 days
6) 2-4 weeks

22
Q

Nosebleed Lab Eval

A

Evaluate the phases of coagulation:

  • Platelet phase:
    1) CBC with platelet count
    2) Platelet fxn tests
    3) bleeding time (also vascular phase)
  • Humoral Phase:
    1) prothrombin time
    2) Partial thromboplastin time
23
Q

PTT normally 34-36 sec. What about a kid with PTT of 38. WHat is DDX? and what is work-up

A

DDX:

  • Lab error
  • Vit K def (Antibiotic, diet)
  • Mild hemophilia or VWD
  • Normal variation
  • Inhibitor

Work-up:
-If recent diet or AB concerns, give vit K for 2 weeks and repeat. If still abnormal, do a mixing study.

24
Q

After a mixing study if you have a:
1) Corrected PTT
2) Uncorrected PTT
What do yo look for

A

1) Factor levels: VWF

2) Inhibitor search: Lupus anticoagulant panel, anticardiolipin IgG and IgM, anti B2 microglobulin

25
Q

1) Classical or Hemophilia A is deficiency of factor ____.

2) Hemophilia B, or christmas disease is deficiency of Factor ____.

A

1) VIII

2) IX

26
Q

How to treat hemophilia

A

-Give factor
~FACTOR VIII: 50 units/kg IV as bolus then 4 units/kg/hr IV continuous infusion startings ASAP after bolus
~FACTOR IX: 100 units/kg IV as bolus then 5 units/kg/hr IV continuous infusion
* In emergencies, give factor BEFORE you image patient.

27
Q

Deficiency of normal VWF fxn due to either deficiency or mutation of the protein. WHat are common subtypes?

A

Type 1: deficiency
Type 2: mutation
type 3: No detectable factor

28
Q

T/F: VWF is estrogen dependent

A

True- important to get menstrual hx. Also bleeding after child birth

29
Q

Von Willebrand Disease prolongs PTT due to deficiency of VIII which is stabilized by VWF. Treatment with:

1) Agent to increase VWF
2) Factor concentrates
3) Antifibrinolytics

A

1) DDAVP (Stimate)
2) Humate P and Alphanate SD
3) Amicar

30
Q

What is Immune Thrombocytopenic Purpura

A

Immune attack on platelets.

  • Opsonization rather than lysis
  • -In pre-pubertal kids, usually post viral infection by a couple of weeks.
  • If platelets drop low enough, small bleeding sites (petechiae) form
  • Acute <1 yr
31
Q

Treatment of Immune Thrombocytopenic Purpura

A

1) Observation
2) IVIG
3) Prednisone
Second line: WInRho SD, Rituxan, Splenectomy