Anemia/Polycythemia Flashcards

1
Q

twin to twin transfusion syndrome

A
  • hemorrhage*
  • occurs in monozygotic, monochorionic twin pregnancies
  • Hgb difference between twins > 5 g/dL
  • often size discrepancy as well: >20% difference with chronic hemorrhage
  • smaller twin has elevated retic count d/t chronic blood loss
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

placental/cord problems

A
  • hemorrhage*
  • umbilical cord rupture
  • cord or placental hematoma
  • anomalous cord insertion
  • rupture of anomalous vessels of cord or placenta
  • accidental incision of cord or placenta
  • placenta previa or placental abruption
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

fetal/maternal hemorrhage

A
  • spontaneous
  • from traumatic amniocentesis
  • external cephalic version?
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

gold standard to detect fetal/maternal hemorrhage?

A

Kleihauer-Betke test

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

Internal causes of hemorrhage

A
  • intracranial (subdural, subarachnoid, intraventricular), smbgaleal
  • organ rupture (liver, spleen, adrenal, kidney)
  • pulmonary
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

external causes of hemorrhage

A
  • phlebotomy

- iatrogenic

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

Rh Blood group incompatibilities

A

hemolysis

also called erythroblastosis fetalis

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

What causes Rh incompatibilities

A

hemolysis
Rh+ fetal cells enter the bloodstream of an Rh- mother resulting in maternal antibody production to the Rh+ fetal cells
-subsequent pregnancies will have destruction of fetal RBCs if the fetus is Rh+

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What to look for in Rh incompatibility?

A
  • hemolysis*
  • anemia: ongoing hemolysis
  • tissue hypoxia, acidosis: decreased oxygen carrying capacity
  • congestive heart failure & hydrops fetalis: generalized edema d/t increased blood volume and cardiac output
  • ascites, pleural effusion: collection of fluid
  • hepatosplenomegaly: increased extramedullary hematopoiesis
  • petechiae: thrombocytopenia
  • hypoglycemia: hyperinsulinemia d/t RBC destruction
  • positive direct coombs test result
  • increased retic count: ongoing hemolysis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

ABO blood group incompatibilities

A
  • hemolysis*

- most commonly seen with O blood type mother carrying fetus with A or B blood type

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

How does ABO incompatibility occur?

A

-can occur with 1st pregnancy d/t to maternal exposure to A & B antigens (food, bacteria, pollen) that results in production of anti-A and anti-B antibodies

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

What to look for in ABO incompatibility?

A
  • mild hemolysis
  • anemia
  • reticulocytosis
  • hyperbili
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How to treat ABO and Rh incompatibilities?

A
  • RhoGAM
  • phototherapy
  • good hydration
  • IVIG 1 gm/kg over 4 hrs
  • consider blood or exchange transfusion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What does RhoGAM do?

A

RhoGAM: for Rh- mothers; prophylactic anti-D immune globulin

-blocks maternal antibody production by destroying fetal red blood cells in maternal circulation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

When should RhoGam be given?

A

-given at 28 weeks, then again within 72 hours following delivery and any time there may be fetal-maternal blood mixing in Rh- pregnant women

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

G6PD (glucose-6-phosphate dehydrogenase deficiency)

A
  • hemolysis*
  • most common inherited red cell disorder
  • sex linked, mainly male offspring, occasional female carriers
  • most common in American black infants, also mediterranean, african, asian descent
17
Q

Pathogenesis of G6PD

A
  • hemolysis*
  • hemolysis and shortened erythrocyte life due to deficiency of red cell enzyme and exposure to antioxidant stress (drugs, infection)
18
Q

Infection

A
  • hemolysis*
  • intrauterine: TORCH (rubella and parvo cause decreased RBC production in addition to hemolysis, thus increased risk for hydrops)
  • postnatal: bacterial infections
  • both may cause hemolysis, anemia, thrombocytopenia, DIC
19
Q

About anemia of prematurity

A

-considered physiologic

20
Q

How does anemia of prematurity happen?

A
  • erythropoietin falls to minimal level d/t improved relative oxygenation after birth
  • Hgb falls by 1 g/dL/week in preterm infants starting at 2 weeks of age to an average nadir of 7-9 g/dL at 6 to 8 weeks of life
  • smaller/more immature infants will reach lower nadir at earlier age d/t shortened RBC life span
  • premature infants have persistent hepatic pathway
  • ensuing anemia triggers a hypoxic stimulus, thus increasing the presence of erythropoietin and ultimately RBC production
21
Q

What to look for with anemia of prematurity?

A
  • symptoms of hypoxia: poor feeding, poor weight gain, dyspnea, tachypnea, tachycardia, diminished activity, pallor, increased A/B events
  • retic count
22
Q

How to treat anemia of prematurity?

A
  • minimize blood losses
  • iron supplementation
  • transfusion
  • EPO
23
Q

Iatrogenic anemia

A

caused by the need for frequent blood sampling of critically ill infants
-removal of >20% of blood volume over 24-48 hours can produce anemia

24
Q

Findings with acute blood loss

A
  • pallor followed by cyanosis and desaturation
  • shallow, rapid, irregular respirations
  • tachycardia
  • weak or absent peripheral pulses
  • low or absent blood pressure
  • acidosis
25
Findings with chronic blood loss
- pallor w/o signs of acute distress - normal blood pressure - low hgb level - possible s/s of CHF w/hepatomegaly
26
What to look for on exam for patients with anemia
- jaundice - cephalohematoma - abdominal distension or mass - petechiae - purpura - murmur - gallop rhythm - hydropic changes
27
polycythemia definition
hemoglobin > 22 g/dL or hematocrit > 65% in the 1st week of life
28
at what point does blood display hyperviscosity properties?
when HCT is > 60%
29
what two congenital disorders that cause polycythemia?
- congenital adrenal hyperplasia | - Beckwith-Wiedemann syndrome
30
what are babies with polycythemia predisposed to?
- hypoglycemia - hypocalcemia - hypomagnesemia
31
polycythemia treatment
- start total fluids higher (100-120 ml/kg/day) - may need saline boluses - may need partial exchange transfusion
32
what is the goal of a partial exchange transfusion for polycythemia?
to reduce HCT to