* This is the Professional Version. *
Traumatic Hemolytic Anemia
(Microangiopathic Hemolytic Anemia)
Patient Education
- Anemias Caused by Hemolysis
- Overview of Hemolytic Anemia
- Autoimmune Hemolytic Anemia
- Embden-Meyerhof Pathway Defects
- Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
- Hemoglobin C Disease
- Hemoglobin E Disease
- Hemoglobin S-C Disease
- Hemoglobin S–Beta-Thalassemia Disease
- Hereditary Spherocytosis and Hereditary Elliptocytosis
- Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Sickle Cell Disease
- Stomatocytosis and Anemia Caused by Hypophosphatemia
- Thalassemias
- Traumatic Hemolytic Anemia
(See also Overview of Hemolytic Anemia.)
Traumatic hemolytic anemia is intravascular hemolysis caused by excessive shear or turbulence in the circulation.
Trauma causes fragmented RBCs (eg, triangles, helmet shapes) called schistocytes in the peripheral blood; their appearance on the peripheral smear is diagnostic. Small schistocytes cause low MCV and high RBC distribution width (the latter reflecting the anisocytosis).
When RBC fragmentation occurs in the setting of microvascular injury, the process is termed microangiopathic hemolytic anemia (MAHA). Causes of fragmentation hemolysis include
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Disseminated intravascular coagulation, a consumptive process secondary to other disorders such as sepsis, malignancy, pregnancy complications, trauma or surgery
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Stenotic or mechanical heart valves, or prosthetic valve dysfunction (ie. perivalvular leak)
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Hemolytic uremic syndrome or related disorders such as the HELLP syndrome (hemolysis, elevated liver enzymes, and low platelet count), and systemic sclerosis renal crisis
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Rare cases of significant repetitive impact, such as foot strike hemolysis (march hemoglobinuria), karate strikes, or hand drumming
Treatment addresses the underlying process. Iron deficiency anemia occasionally is superimposed on the hemolysis as a result of chronic hemosiderinuria and, when present, responds to iron-replacement therapy.
Resources In This Article
- Anemias Caused by Hemolysis
- Overview of Hemolytic Anemia
- Autoimmune Hemolytic Anemia
- Embden-Meyerhof Pathway Defects
- Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
- Hemoglobin C Disease
- Hemoglobin E Disease
- Hemoglobin S-C Disease
- Hemoglobin S–Beta-Thalassemia Disease
- Hereditary Spherocytosis and Hereditary Elliptocytosis
- Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Sickle Cell Disease
- Stomatocytosis and Anemia Caused by Hypophosphatemia
- Thalassemias
- Traumatic Hemolytic Anemia
* This is the Professional Version. *





Kimia
Meghan