HAEMOLYSIS Flashcards

1
Q

DESCRIBE THE CLINICAL CONSEQUENCES OF IVH HAEMOLYSIS

IVH- Intravascular Haemolysis

A
  1. Anaemia due to Iron Deficiency
  2. Leg Ulcers
  3. Megaloblastic Anaemia
  4. Arterial Renal Failure
  5. Pulmonary Hypertension
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2
Q

Laboratory tests

List the laboratory findings in Intravascular haemolysis

A
  1. Decreased Haptoglobin
  2. Plasma Hb
  3. Haemoglobinuria
  4. Haemosiderinuria (Haemo-side-rin-uria)
  5. Increased LDH
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3
Q

DESCRIBE/LIST THE CLINICAL CONDITIONS WITH PREDOMINANT INTRAVASCULAR HAEMOLYSIS

A
  1. Malaria
  2. Sickle Cell Disease (SCD)
  3. Cold Autoimmune Haemolytic Anaemia
  4. Immediate Blood Transfusion Reaction
  5. Paroxysmal Nocturnal Haemoglobinuria
  6. Macro/Micro- Angiopathic Haemolytic Anaemia
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4
Q

Describe the Clinical Consequences Of Extravascular Haemolysis

Remeber extravascular occurs outside blood vessels( in spleen, liver…)

A

1.Anaemia
2.Splenomegaly
3.Leg Ulcers
4.Jaundice
5.Gall Stones
6.Iron Overload
7.Megaloblastic Anaemia
8.Pulmonary Hypertension

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5
Q

Lab Tests for EVH

Describe the Lab Test FIndings that could indicate Extravascular Haemolysis.

A
  1. Increased Unconjugated Bilirubin (acholuric Jaundice)
  2. Increased LDH
  3. Decreased Serum Haptoglonin
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6
Q

Discuss the Clinical Conditions with predominant Extravascular Haemolysis

A
  1. Beta thalassaemia major.
  2. HbH disease.
  3. Hereditary Spherocytosis.
  4. Warm Auto-Immune Haemolytic Anaemia.
  5. Delayed Blood Transfussion Reaction.
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7
Q

Describe the differences in clinical features in EVH and IVH

A
  1. both have Anaemia
  2. There’s Iron deficiency in Intravascular and Iron Overload in Extravascular
  3. There’s Jaundice in Extravascular and NO JAUNDICE in Intravascular
  4. NO Zinc Deficiency in Extravascular and Zinc Deficiency in present in Intravascular
  5. There’s definitely present Gall Stones in extravascular
  6. There’s Definitely present Pulmonary Hypertension in Intravascular
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8
Q

Discuss the causes of Microangiopathic Haemolysis

A
  1. Disseminated Intravascular Coagulation
  2. Thrombotic Thrombocytopenic Purpura (TTP)
  3. Haemolytic Uraemic Syndrome
  4. Malignant Hypertension
  5. Disseminated Carcinoma
  6. Immunogenic Vasculitis, eg, SLE
  7. Giant Haemangioma
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9
Q

Describe the Pathogenesis and Clinical Features of Hereditary Spherocytosis

A

Pathogenesis
The red cell assumes a spherical shape due to the loss of typical biconcave conformation

The clinical presentation is variable, but patients with HS will typically have Splenomegaly and Fluctuating Jaundice

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