Hemoglobin M disease; Erythrocyte reductase deficiency; Generalized reductase deficiency
A medicine called methylene blue is used to treat persons with severe methemoglobinemia. Note: Methylene blue may be dangerous in patients who have or may be at risk for a blood disease called G6PD deficiency, and should not be used. If you or your child have G6PD deficiency, always tell the health care provider before treatment is given.
Ascorbic acid may also be used to reduce the level of methemoglobin.
Alternative treatments include hyperbaric oxygen therapy and exchange transfusions.
In most cases of mild acquired methemoglobinemia, no treatment is required, other than avoiding the medicine or chemical that caused the problem. Treatment, such as a blood transfusion, may be needed in severe cases.
People with Type 1 methemoglobinemia and hemoglobin M disease usually do well. Type 2 methemoglobinemia is much more serious, and usually causes death within the first few years of life.
People with acquired methemoglobinemia usually do very well once the drug, food, or chemical that caused the problem is avoided.
Call your health care provider if there is a family history of methemoglobinemia and you develop symptoms of this disorder.
Call your health care provider or emergency services immediately if there is severe shortness of breath.
DeBaun MR, Vichinsky E. Hemoglobinopathies. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 18th Ed. Philadelphia, PA: Saunders Elsevier; 2007: chap 462.
Gregg XT, Prchal JT. Red Blood Cell Enzymopathies. In: Hoffman R, Benz EJ Jr., Shattil SJ, Furie B, Cohen HJ, eds. Hematology: Basic Principles and Practice. 4th ed. Philadelphia, PA: Churchill Livingston Elsevier; 2005: chap 39.