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Anemia In Pregnancy
Definition:
Hb = 10 gm/dl or less
Hct = 35%
Incidence:
< 5% of pregnant ladies
Significance:
Fetal Morbidity & Mortality
Infection rate
Decompensation in mothers w/ Cardiac or Pulmonary
dis
Exacerbate the effect of Hemorrhage
Delays recovery in the Post Partum period
General Symptoms of Anemia :
1- Lethargy.
2- Tiredness.
3- Headache.
4- Dizziness.
5- Dyspnea.
6- Dysphagia. IDA
7- Palpitation: b/c blood volume in pregnancy physiological
tachycardia.
8-
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Intake
poor diet
Hyperemesis gravidarum esp in early
pregnancy
storage
liver disease
Clinical classification:
1- Iron deficiency anemia.
85%
2- Megaloblastic anemia.
3- Secondary anemia (2%):
- Chronic infections specially pyelonephritis.
- Recurrent bleeding.
- Malignancy.
4- Hemolytic anemia:
- SCD (3.5%).
- Thalassemia.
5- Aplastic anemia, which is rare these days.
After
After
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Iron Sources:
1- Red meat, liver and kidneys.
2- Green leaves and vegetables.
3- Fruits like Banana.
Iron Absorption:
Site = Upper small intestine = duodenum &
jejunum
Amount = 1/10th dietary iron
Iron Storage:
Site = RES
Amount = 30%
Form = Hemosiderine
Iron Excretion:
Route = urine, feces, menstrual bl, skin
desquamation
Amount = 1mg/day
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# Note
The iron loss starts with depletion of iron stores
~ iron serum levels (10 gm/dl)
~ iron binding capacity (16)
~ morphologic changes in RBCs microcytic hypo
chromic.
Investigations:
1- CBC (microcytic hypo chromic).
2- Serum iron- (NL= 34-150).
3- Serum ferritin- (NL = 6-31)
4- TIBC
5- Bone marrow if needed
Recommendation:
1- Adequate diet rich in iron = 15 mg/day
2- Iron prophylaxis.
Treatment:
Depends on severity of anemia and gestational age:
1- In late 3rd trimester & severe anemia (<6)
~ blood transfusion (packed RBCs).
Then continue with iron supplement.
B/c if she goes into labor and develops PPH, she will
collapse & die.
B/c the effect of iron therapy will not appear before 4-6
weeks.
~ to anticipate the complications after delivery
2- Any stage of pregnancy & severe anemia
~ transfuse her first to make her feel healthier
then continue with iron supplement.
3- Moderate anemia (6-8gm/dl)
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iron therapy., & no transfusion
IM injection:
3 Z- shaped injections every week
SE: * Very painful.
* staining of the injection site in the
buttock
esp in fair color women
* abscess formation.
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After 4-6 weeks
b/c it takes 4-6 weeks to notice a change in Hb.
Reticulocyte count
After 10 days from starting iron we
if 3% or more responding to the iron therapy.
Megaloblastic anemia
# due to folic acid rather than B12.
# Its also more commonly found in association with iron deficiency
anemia.
Folic Acid Physiology:
Diet rich in folic acid:
1- Animal liver and meat,
2- Green vegetables (dont cook it).
3- Peanuts.
Requirements:
WHO recommend to give folic acid 300 g throughout
pregnancys prophylaxis
Absorption site:
upper 1/3 of small intestine
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Causes :
Requirements Multiple pregnancy
Multiparity
frequency of pregnancy ( < 2 y apart)
Utilization
Analgesics
ABC e.g Furadantin used for UTI.
Contraceptive pills
Methetroxate
Phenytoin.
Intake
poor diet
Hyperemesis gravidarum esp in early pregnancy
storage
liver disease
Presentation:
Pallor.
Glossitis
Oral fissures
Edema of ankle & feet
Vomiting & diarrhea
Splenomegaly
Check forBP & proteinuria.
Check for neural tube defect esp.if mother has
polyhydramnios.
Investigations
1- CBC:
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Megaloblastic (macrocytosis).
Anisocytosis
Giant cells
Howell Jolly bodies
Thrombocytopenia
Neutropenia
Hyper-segmented neutrophils.
# Note**
If the patient has vitamin B12 deficiency (pernicious
anemia) and you give her folic acid, Hb levels will improve
but later on she will develop sub acute combined
degeneration of the spinal cord.
So, if you diagnose megaloblastic anemia give folic acid +
vitamin B12.
Then after pregnancy is over you investigate for pernicious
anemia by
** schilling test
** radio-isotopes which is harmful to the fetus.
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Prophylaxis:
Prophylactic folic acid w/ iron in the combined pill = 0.5
mg/day
Hemoglobinopathies
Pathology:
- Alteration in the amino acid structure of the polypeptide
chain
e.g. HbS Sickle cell disease
HbC Hemolytic anemia
- Impaired production of orchains
ka Thalassemia
Clinical Manifestations depends on:
1- Type of Hb present
2- Relative proportion , depending on inheritance
i.e. Homo or Hetero zygous
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3- UTI infection ( pyelonephritis) is common in these
patients esp. in sickle cell trait rather than disease.
4- HTN
5- HSM
6- Leg ulceration
7- If the mother develop hypoxia, dehydration or acidosis
its going to affect the baby.
Management:
1- Avoid risk factors
2- Avoid iron b/c 1- Serum iron
2- TIBC
Hemosiderosis
7- Rx Crisis *
*
*
*
*
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Thalassemia
Management:
1- Folic acid supplements
2- Blood transfusion depending on Hb