Related Questions

A man whose blood group is not known meet with a serious accident and needs blood transfusion immediately. Which one of the blood group mentioned below and readily available in the hospital will be safe for transfusion?
A O, Rh-
B O, Rh+
C AB, Rh-
D AB, Rh+
Administering a vaccine provides protection by inducing synthesis of antibodies (proteins) specific of the vaccine. The cell in the body responsible for the production of antibodies is
A Granulocyte
B Lymphocyte
C Erythrocyte (red blood cell)
D Platelet
Immediate blood transfusion reaction includes :
A Hypokalaemia
B Circulating over load
C Air embolism
D Hypercalcemia
Which test can be used to detect haemolytic anemia
A Coomb’s test
B Peripheral blood smear examination
C Reticulocyte count
D Occult blood test
E Schilling test
Following statement(s) is (are) true regarding haemolytic uraemic syndrome (HUS)
A Antibiotics may paradoxically increase shiga toxin release
B Eculizumab blocks complement activities by cleavage of C5
C Plasma exchange significantly improve the outcome
D Microangiopathic hemolytic anaemia is a characteristic feature
E Rickettsial infection associated with diarrhoea associated (D+) HUS
Haemolytic uremic syndrome is characterized by
A Microangiopathic haemolytic anaemia
B Azotemia
C Thrombocytopenic purpura
D Leukocytoclastic vasculitis
E Arthritis
The followings are the components of haemolytic Uraemic syndrome
A Uremia
B Hemolytic anemia
C Thrombocytopenia
D Heart failure
E Leucopenia
Haemolytic jaundice is associated with
A Increase in the concentration of bilirubin diglucoronide in the bile
B Increase in urobilinogen in urine
C Presence of bilirubin in urine
D Increase in the serum alkaline phosphatase
E Decrease in unconjugated bilirubin in the serum
Haemolytic disease of newborn HDN is associated with involvement of
A IgG
B IgG + complement
C IgM
D IgA
E IgD
Haemolytic diseases of the newborn include
A ABO incompatibility
B Vitamin K1 deficiency
C Glucose-6-phosphate dehydrogenase deficiency
D Sickle cell trait
E Hereditary spherocytosis

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