Module 9: Part 3 (46-67) Flashcards

1
Q

air embolism signs and symptoms

A

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

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

During normal pregnancy, plasma volume increases by approximately

A

50%

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

red blood cell (RBC) mass increases by only 30%; this differential increase
results in the

A

physiologic anemia of pregnancy

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

Iron deficiency is the most common cause of anemia in pregnancy

A

iron deficiency

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

During the first trimester it increases the risk for preterm delivery and low
birth weight

A

iron deficiency

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

iron deficiency lab findings

A

Reduced hematocrit, low mean corpuscular volume (MCV), low total serum
iron, ferritin, and transferrin saturation

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

A group of microcytic, hemolytic anemias that
results from the reduced synthesis of one or more of
the polypeptide globin chains

A

Thalassemias

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

The reduced synthesis of polypeptide globin chains in thalassemia leads to:

A

An imbalance in globin chain ratios
Defective hemoglobin
Erythrocyte damage resulting from excess globin
subunits

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

Thalassemia transfusion dependent

A

require ongoing transfusions
for survival

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

Thalassemia non-transfusion dependent

A

may require transfusions
during stressors such as infection or pregnancy

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

Four types of thalassemia (four genes
2 on each chromosome 16) that
produce α chains

A

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)

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

not at increased risk for adverse outcomes during
pregnancy or surgery, MCV of 78 85 fL

A

Silent carrier(3 functioning genes)

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

usually have mild anemia, MCV of 70 75 fL , typically
asymptomatic and no additional risk for adverse
outcomes in pregnancy or surgery

A

α-thalassemia trait(2 functioning genes)

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

moderately severe microcytic anemia,
splenomegaly, fatigue, and generalized
discomfort, these patients may be transfusion
dependent

A

Hemoglobin H disease(1 functioning gene):

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

incompatible with life, fetus usually dies in
utero or shortly afterward of hydrops fetalis

A

α0- thalassemia or Bart’s hydrops(no functioning
genes)

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

Hydrops Fetalis

A

Severe edema in an unborn
baby or newborn

50% don’t survive

Immune (Rh neg mom/Rh
positive baby)and nonimmune
type

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

β-Thalassemias

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Types of β-Thalassemias (3)

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

β-thalassemia major pts and their chances of getting pregnant

A

It is unusual for these patients to get pregnant

But…..transfusion and chelation therapy can improve fertility and reproductive
therapies can help

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

These patients can have increased incidence of spontaneous abortion, intrauterine fetal
death and growth restriction

A

β-thalassemia major pts

21
Q

β-thalassemia major, patient goals

A

Metabolic demands of pregnancy increase transfusion requirements

Goal: maintain a hemoglobin above 10 g/dL

22
Q

Chelation agents are stopped in the first trimester for pts with

A

β-thalassemia major

23
Q

Incidence of fetal growth restriction and oligohydramnios are more common

A

β-thalassemia minor

24
Q
A

Usually benign
Anemia is typically mild (Hgb 9
11 g/dL)
Most tolerate pregnancy well
High dose folate during first trimester
Incidence of fetal growth restriction and oligohydramnios are more common
Does not affect anesthetic management during labor cesarean delivery
Moderate anemia during periods of stress (infection, pregnancy)

25
Q

Hemoglobinopathy characterized by a homozygous mutation (hemoglobin S)
where valine is substituted for glutamic acid in the B chain

A

Sickle Cell Disorder

26
Q

refers to a state in which erythrocytes undergo sickling when
they are deoxygenated

A

Sickle cell disease

27
Q

refers to disorders in which sickling results in clinical signs and
symptoms; genotypes include hemoglobin SS (Hb SS) disease, hemoglobin SC (Hb
SC) disease and sickle cell β thalassemia (there are other genotypes)

A

Sickle cell disease

28
Q

Factors that can increase the sickling risk (Sickle cell anemia): (5)

A

Hemoglobin S concentration greater than 50% of
total hemoglobin
Dehydration leading to increased blood viscosity
Hypotension causing vascular stasis
Hypothermia
Acidosis

29
Q

Hemoglobin S is the main hemoglobin in the disease

A

Sickle cell anemia

30
Q

___ tension is the most important determinate
in sickling

A

Oxygen

31
Q

Diagnosis and Treatment of Sickle cell anemia

A

Couples with high risk for sickle cell disease should
have prenatal screening for abnormal hemoglobin

Blood transfusions (only when necessary for acute
anemia, aplastic crisis, acute chest syndrome,
pneumonia with hypoxemia before or during
surgery)

Goal is a hemoglobin above 8 g/dL

32
Q

In the adult, sickle cell anemia is characterized by:

A

Hemoglobin of 6
8 g/dL
Elevated reticulocyte count
Presence of sickle cells on the peripheral blood smear
(elongated and crescent shaped vs biconcave)

33
Q

Couples with high risk for sickle cell disease should
have ….

A

prenatal screening for abnormal hgb

34
Q

Pregnancy typically exacerbates the complications
of

A

sickle cell anemia

35
Q

serious complications of sickle cell anemia

A

Thromboembolic complications, infection,
cardiomyopathy, and pulmonary hypertension are
the most serious maternal medical complications

36
Q

Increased incidence of preterm labor, placental
abruption, fetal growth restriction, preeclampsia,
and eclampsia

A

sickle cell anemia

37
Q

sickle cell anemia management

A

OB: Antenatal ASA to reduce preeclampsia risk,
thromboprophylaxis:maternal and fetal surveillance

Early preparation of crossmatched blood products
should be considered

Blood transfusions are given only if indicated (acute
anemia, crisis) with the goal of hemoglobin >8 g/dL

38
Q

Anesthetic management of sickle cell anemia (8)

A

Focus on recent sickle cell disease exacerbations and
the causes or precipitating factors
CBC to check the level of anemia
Check for chronic end organ injury
Crystalloid to maintain intravascular volume
Transfusions as needed to maintain RBCs to maintain oxygen carrying capacity
Supplemental O2
Normothermia, prevent venous stasis, venous thromboembolism therapy
Pain control during labor/cesarean

39
Q

Normal hemostasis involves 3 processes
almost simultaneously

A
  1. Primary hemostasis (formation of a
    friable platelet plug)
  2. Coagulation or secondary hemostasis
    (reinforcement of the friable platelet
    plug by the formation of a firm fibrin
    clot)
  3. Fibrinolysis (clot lysis and restoration of
    blood flow through the recanalized
    vessel)
40
Q

The increase in the concentration of most
coagulation factors is a/w a
shortening of the ___ & ___ during normal
pregnancy

A

PT and aPTT

41
Q

Fibrinogen and fibrin degradation products are
(increased/decreased)in normal pregnancy

A

increased

42
Q

Thrombocytopenia is a sensitive, but not
specific, indicator of

A

DIC

43
Q

Gestational thrombocytopenia (GT)

A

is the most common cause of thrombocytopenia
in pregnancy

44
Q

Usually considered a platelet count below 150

A

Gestational thrombocytopenia (GT)

45
Q

A small subset of women with ______ may develop more significant declines in platelet
count and reduction in antithrombin III associated with preeclampsia, HELLP
syndrome or acute fatty liver of pregnancy, ITP

A

Gestational thrombocytopenia (GT)

46
Q

(ATP) IgG antibodies are
responsible for the increased platelet destruction

A

Autoimmune Thrombocytopenic Purpura
(ATP)

47
Q

Antibodies directed against platelet antigens are produced primarily in
the ____, where phagocytosis by macrophages occur

A

spleen

48
Q

______ are administered if the platelet count is < 20- 30k before the onset of labor or <50k at the time of delivery

A

Corticosteroids

49
Q

High dose IV ____ if no response to steroids in Thrombocytopenic Coagulopathies

A

immune globin