Module 9: Part 3 (46-67) Flashcards
air embolism signs and symptoms
Sudden and dramatic
Hypotension, hypoxemia, dyspnea
Chest pain during uterine repair (what else does this
sound like?)
Millwheel murmur
Right sided heart failure, rhythm changes
During normal pregnancy, plasma volume increases by approximately
50%
red blood cell (RBC) mass increases by only 30%; this differential increase
results in the
physiologic anemia of pregnancy
Iron deficiency is the most common cause of anemia in pregnancy
iron deficiency
During the first trimester it increases the risk for preterm delivery and low
birth weight
iron deficiency
iron deficiency lab findings
Reduced hematocrit, low mean corpuscular volume (MCV), low total serum
iron, ferritin, and transferrin saturation
A group of microcytic, hemolytic anemias that
results from the reduced synthesis of one or more of
the polypeptide globin chains
Thalassemias
The reduced synthesis of polypeptide globin chains in thalassemia leads to:
An imbalance in globin chain ratios
Defective hemoglobin
Erythrocyte damage resulting from excess globin
subunits
Thalassemia transfusion dependent
require ongoing transfusions
for survival
Thalassemia non-transfusion dependent
may require transfusions
during stressors such as infection or pregnancy
Four types of thalassemia (four genes
2 on each chromosome 16) that
produce α chains
Silent carrier(3 functioning genes)
α-thalassemia trait(2 functioning genes)
Hemoglobin H disease(1 functioning gene)
α0- thalassemia or Bart’s hydrops(no functioning
genes)
not at increased risk for adverse outcomes during
pregnancy or surgery, MCV of 78 85 fL
Silent carrier(3 functioning genes)
usually have mild anemia, MCV of 70 75 fL , typically
asymptomatic and no additional risk for adverse
outcomes in pregnancy or surgery
α-thalassemia trait(2 functioning genes)
moderately severe microcytic anemia,
splenomegaly, fatigue, and generalized
discomfort, these patients may be transfusion
dependent
Hemoglobin H disease(1 functioning gene):
incompatible with life, fetus usually dies in
utero or shortly afterward of hydrops fetalis
α0- thalassemia or Bart’s hydrops(no functioning
genes)
Hydrops Fetalis
Severe edema in an unborn
baby or newborn
50% don’t survive
Immune (Rh neg mom/Rh
positive baby)and nonimmune
type
β-Thalassemias
The production of β chains is reduced
Have only one gene on each chromosome 11
Usually have an excess of alpha chains that accumulate in RBC precursors
Types of β-Thalassemias (3)
β0 thalassemia also known as β thalassemia major or Cooley’s anemia there is no beta
chain formation
Thalassemia intermedia
β thalassemia also known as β thalassemia minor
β-thalassemia major pts and their chances of getting pregnant
It is unusual for these patients to get pregnant
But…..transfusion and chelation therapy can improve fertility and reproductive
therapies can help