Rh Incompatibility and Disease

Содержание

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Rh Disease Occurs during pregnancy when there is an incompatibility between

Rh Disease

Occurs during pregnancy when there is an incompatibility between the

blood types of the mother and fetus
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Blood Types A, B, O blood groups are specific types of

Blood Types

A, B, O blood groups are specific types of proteins

found on the surface of RBC’s
Also found in the cells and other body fluids (saliva, semen, etc)
O represents neither protein being present on RBC
Possible groups include: A, B, AB, or O
A, B, O groups most important for transfusions
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Rh Factor Proteins (antigens) occurring only on surface of RBC’s Rh

Rh Factor

Proteins (antigens) occurring only on surface of RBC’s
Rh + if

proteins present
Rh – if proteins absent
A+, A-, B+, B-, AB+, AB-, O+, O-
Most important for pregnancy
Inheritance is Autosomal Dominant
15% Caucasian population is Rh-
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Nomenclature Correct to say Rh(D) + or – Rh blood system

Nomenclature

Correct to say Rh(D) + or –
Rh blood system has other

antigens: C, c, D, E, e
D is by far the most common and the only preventable one
Weak D (Du) also exists
Also non Rhesus groups such as Kell, MNS, Duffy (Fy) and Kidd (Jk) exist
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Why Does Rh Status Matter?

Why Does Rh Status Matter?

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Pathophysiology Rh(D) antigen expressed by 30 d GA Many cells pass

Pathophysiology

Rh(D) antigen expressed by 30 d GA
Many cells pass between maternal

& fetal circulation including at least 0.1 ml blood in most deliveries but generally not sufficient to activate immune response
Rh antigen causes > response than most
B lymphocyte clones recognizing foreign RBC antigen are formed
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Pathophysiology cont… Initial IgM followed by IgG in 2 wks- 6

Pathophysiology cont…

Initial IgM followed by IgG in 2 wks- 6 mths
Memory

B lymphocytes activate immune response in subsequent pregnancy
IgG Ab cross placenta and attach to fetal RBC’s
Cells then sequestered by macrophages in fetal spleen where they get hemolyzed
Fetal anemia
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Causes of RBC Transfer abortion/ectopic partial molar pregnancy blighted ovum antepartum

Causes of RBC Transfer

abortion/ectopic
partial molar pregnancy
blighted ovum
antepartum bleeding
special procedures

(amniocentesis, cordocentesis, CVS)
external version
platelet transfusion
abdominal trauma
inadvertent transfusion Rh+ blood
postpartum (Rh+baby)
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General Screening ABO & Rh Ab @ 1st prenatal visit @

General Screening

ABO & Rh Ab @ 1st prenatal visit
@ 28 weeks
Postpartum
Antepartum

bleeding and before giving any immune globulin
Neonatal bloods ABO, Rh, DAT
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Gold Standard Test Indirect Coombs: -mix Rh(D)+ cells with maternal serum

Gold Standard Test

Indirect Coombs:
-mix Rh(D)+ cells with maternal serum
-anti-Rh(D) Ab will

adhere
-RBC’s then washed & suspended in Coombs serum (antihuman globulin)
-RBC’s coated with Ab will be agglutinated
Direct Coombs:
-mix infant’s RBC’s with Coombs serum
-maternal Ab present if cells agglutinate
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+ Rh(D) Antibody Screen Serial antibody titres q2-4 weeks If titre

+ Rh(D) Antibody Screen

Serial antibody titres q2-4 weeks
If titre ≥1:16

- amniocentesis or MCA dopplers and more frequent titres (q1-2 wk)
Critical titre – sig risk hydrops
** amnio can be devastating in this setting
U/S for dating and monitoring
Correct dates needed for determining appropriate bili levels (delta OD450)
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U/S Parameters Non Reliable Parameters: Placental thickness Umbilical vein diameter Hepatic

U/S Parameters

Non Reliable Parameters:
Placental thickness
Umbilical vein diameter
Hepatic size

Splenic size
Polyhydramnios
Visualization of walls of fetal bowel from small amounts intraabdominal fluid may be 1st sign of impending hydrops
U/S reliable for hydrops (ascites, pleural effusions, skin edema) – Hgb < 70
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Amniocentesis Critical titre/previous affected infant Avoid transplacental needle passage Bilirubin correlates

Amniocentesis

Critical titre/previous affected infant
Avoid transplacental needle passage
Bilirubin correlates with fetal hemolysis

optical density of amniotic fluid @ 450nm on spectral absorption curve
Data plotted on Liley curve
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Liley Curve Zone I – fetus very low risk of severe

Liley Curve

Zone I – fetus very low risk of severe fetal

anemia
Zone II – mild to moderate fetal hemolysis
Zone III – severe fetal anemia with high probability of fetal death 7-10 days
Liley good after 27 weeks
98% sensitive for detecting anemia in upper zone 2/ zone 3
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Middle Cerebral Artery Dopplers Measures peak velocity of blood flow Anemic

Middle Cerebral Artery Dopplers

Measures peak velocity of blood flow
Anemic fetus preserves

O2 delivery to brain by increasing flow
Sensitivity of detecting severe anemia when MCA >1.5 MoM approaches 100%
Not reliable > 35 weeks GA
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Fetus at Risk Fetal anemia diagnosed by: amniocentesis cordocentesis ultrasound hydrops

Fetus at Risk

Fetal anemia diagnosed by:
amniocentesis
cordocentesis
ultrasound
hydrops

middle cerebral artery Doppler
Treatment:
intravascular fetal transfusion
preterm birth
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Infant at Risk Diagnosis: history of HDN antibodies? early jaundice cord

Infant at Risk

Diagnosis:
history of HDN antibodies?
early jaundice < 24

hours
cord DAT (“Coomb’s”) positive (due to HDN or ABO antibodies)
Treatment:
Phototherapy
Exchange or Direct blood transfusion
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