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Aplastic Crisis
DefinitionDefinition of Aplastic Crisis An aplastic crisis should not be confused with hemolytic anemia, which is a constant feature of sickle cell disease. The aplastic crisis is temporary cessation of red cell production. Because of the markedly shortened red cell survival time in patients with sickle cell disease, a precipitous drop in hemoglobin occurs in the absence of adequate reticulocytosis. SymptomsSymptoms of Aplastic Crisis
CausesCauses of Aplastic Crisis Your body can stop making red blood cells when infected with a virus called parvovirus. This virus is different from the one found in dogs. It is a common virus among children. The virus is spread by people coughing or sneezing into the air. Most of the time you do not even know you were exposed to it. Parvovirus can be spread easily but is usually not harmful to others. However, it can cause problems in people who are pregnant or have sickle cell disease. DiagnosisDiagnosis of Aplastic Crisis The diagnosis of transient aplastic crisis due to parvovirus B19 is often presumptive, based on a falling hemoglobin value and a low reticulocyte count in a patient with a hemolytic anemia. Specific DNA probes allow definitive diagnosis by PCR since the viremia is robust. A rising IgM antibody to the virus is another means of diagnosing parvovirus B19 infection. TreatmentTreatment of Aplastic Crisis Transient aplastic crisis usually is self-limiting and requires only supportive measures. Rare patients require more than a single transfusion to bridge the gap between marrow suppression and recovery. The fact that the BFU-E’s are not suppressed by the virus means that the bone marrow is poised for a rapid response once the virus is tamed. Rare patients will need immunoglobulin treatment, which is dramatically effective in reversing the aplasia. Immunoglobulin concentrate is the treatment of choice and is delivered as 0.4 g/kg/day for 5 days. Find Diseases Alphabetically
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