HAEMOLYSIS Flashcards
DESCRIBE THE CLINICAL CONSEQUENCES OF IVH HAEMOLYSIS
IVH- Intravascular Haemolysis
- Anaemia due to Iron Deficiency
- Leg Ulcers
- Megaloblastic Anaemia
- Arterial Renal Failure
- Pulmonary Hypertension
Laboratory tests
List the laboratory findings in Intravascular haemolysis
- Decreased Haptoglobin
- Plasma Hb
- Haemoglobinuria
- Haemosiderinuria (Haemo-side-rin-uria)
- Increased LDH
DESCRIBE/LIST THE CLINICAL CONDITIONS WITH PREDOMINANT INTRAVASCULAR HAEMOLYSIS
- Malaria
- Sickle Cell Disease (SCD)
- Cold Autoimmune Haemolytic Anaemia
- Immediate Blood Transfusion Reaction
- Paroxysmal Nocturnal Haemoglobinuria
- Macro/Micro- Angiopathic Haemolytic Anaemia
Describe the Clinical Consequences Of Extravascular Haemolysis
Remeber extravascular occurs outside blood vessels( in spleen, liver…)
1.Anaemia
2.Splenomegaly
3.Leg Ulcers
4.Jaundice
5.Gall Stones
6.Iron Overload
7.Megaloblastic Anaemia
8.Pulmonary Hypertension
Lab Tests for EVH
Describe the Lab Test FIndings that could indicate Extravascular Haemolysis.
- Increased Unconjugated Bilirubin (acholuric Jaundice)
- Increased LDH
- Decreased Serum Haptoglonin
Discuss the Clinical Conditions with predominant Extravascular Haemolysis
- Beta thalassaemia major.
- HbH disease.
- Hereditary Spherocytosis.
- Warm Auto-Immune Haemolytic Anaemia.
- Delayed Blood Transfussion Reaction.
Describe the differences in clinical features in EVH and IVH
- both have Anaemia
- There’s Iron deficiency in Intravascular and Iron Overload in Extravascular
- There’s Jaundice in Extravascular and NO JAUNDICE in Intravascular
- NO Zinc Deficiency in Extravascular and Zinc Deficiency in present in Intravascular
- There’s definitely present Gall Stones in extravascular
- There’s Definitely present Pulmonary Hypertension in Intravascular
Discuss the causes of Microangiopathic Haemolysis
- Disseminated Intravascular Coagulation
- Thrombotic Thrombocytopenic Purpura (TTP)
- Haemolytic Uraemic Syndrome
- Malignant Hypertension
- Disseminated Carcinoma
- Immunogenic Vasculitis, eg, SLE
- Giant Haemangioma
Describe the Pathogenesis and Clinical Features of Hereditary Spherocytosis
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