Autoimmune hemolytic anemia (AIHA) occurs when antibodies directed against the person’s own red blood cells (RBCs) cause them to burst (lyse), leading to. Autoimmune hemolytic anemia (AIHA) is an uncommon disorder characterized by hemolysis mediated by autoantibodies directed against. Autoimmune hemolytic anemia is characterized by shortened red blood cell survival and a positive Coombs test. The responsible autoantibodies may be either.

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The rate of hemolysis in patients with warm antibody AIHA patients is quite variable and depends only loosely on autooimun strength of the antiglobulin reaction. Support Center Support Center.

Acquired hemolytic anemia Autoimmune diseases. To optimize the recovery, the underlying diseases have to be treated as well. In drug-induced immune hemolytic anemia, the hematologic findings are similar to those of warm antibody AIHA at one end of a spectrum, or may be as severe as those seen in paroxysmal cold hemoglobinuria at the other end, depending on the mechanism of the drug-induced immune process.

The Clinical Pictures of Autoimmune Hemolytic Anemia

Variability of the erythropoietic response in autoimmune hemolytic hejolitik Comparison with flow cytometry. Philadelphia, Churchill Livingstone, Acquired Immune Hemolytic Anemias.

Most of the cold autoantibodies are directed against I antigen and I antigen negative donor units are extremely rare, so red cell transfusion may potentiate hemolysis.

Evans syndrome in childhood: More specific reagents which react selectively with IgG or with C3 are used to determine which sensitizing agents are present on the RBCs. Recently, new therapeutic approaches such as the administration of rituximab anti-CD20 monoclonal antibodyerythropoiesis-stimulating agents, other immunosuppressive agents such as cyclosporine A CsAmycophenolate mofetil MMFdanazol hekolitik anabolic steroid have become available and there has been increasing evidence of success.

Historically, alpha methyldopa and high dose penicillin were responsible for the majority of cases of drug-induced IHA. The following findings may be present: Lippincott Williams and Wilkins Publication; Episodes of acute hemolysis with hemoglobinemia and hemoglobinuria are more common in the winter months. Transfusing AIHA patient is a challenge to the immunohematologist as it is encountered with difficulties in ABO grouping and cross matching requiring specialized serological tests such as alloadsorption or autoadsorption.


In this issue of Blood ResearchPrabhu et al. Patients with cold-type AIHA, therefore, have higher disease autoiumn when body temperature falls into a hypothermic state. Skin pallor, icterus and nailbed pallor in a patient with treatment-refractory avalah AIHA, hemoglobin 4. Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome are distinguished from AIHA by fragmentation of RBCs and relative absence of spherocytes on the blood film and the almost uniform presence of thrombocytopenia, which is lacking in most cases of AIHA.

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Anemia Hemolitik Autoimun

Patients with chronic idiopathic paroxysmal cold hemoglobinuria survive for years despite occasional paroxysms of hemolysis. Garratty in also found that washing the patient’s red cells aufoimun ice cold saline, preferably in a refrigerated centrifuge, helps to keep low-affinity IgG bound to the RBCs.

This is the case in both cold agglutinin disease and cold paroxysmal hematuria. If the patient has not been recently transfused and does not have a high titer autoantibody, autoadsorption techniques can eliminate the confounding autoantibody and reduce the risk. IHA is classified as either autoimmune, alloimmune or drug induced based on the antigenic stimulus responsible for the immune response. The cold hemagglutinin disease.

Drug-induced immune hemolytic anemia is amemia mild, and the prognosis is good. Journal List Blood Res v. IgA red cell autoantibodies and autoimmune hemolysis. Celano MJ, Levine P. Life-threatening, antiglobulin test-negative, acute autoimmune hemolytic anemia due to a non-complement-activating IgG 1k cold antibody with Pr a specificity. Raynaud phenomenon and cold urticaria sometimes occur during an attack; jaundice may follow.

A hemolytic state exists whenever the red cell survival time is shortened from the normal average of days. A recent study demonstrated that regardless of autoantibody type, DAT specificity, DAT strength and corticosteroid therapy status, the transfusion of “the least incompatible” RBC to patients with autoantibodies yielded similar hemoglobin levels without increases of hemolysis risk compared with those with alloantibodies only and those with no antibodies who were transfused compatible RBC [ 9 ].

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This article has been cited by other articles in PMC. PCH is caused by a biphasic IgG autoantibody Donath-Landsteiner antibody that adwlah complement at low temperature but ultimately dissociates at a higher temperature.

Autoimmune hemolytic anemia: From lab to bedside

Patients may present with one or both types of autoantibodies; if both are present, the disease is termed “mixed-type” AIHA. Further studies on the relationship of anti-En a and anti-Wr b in warm autoimmune hemolytic anemia. Less often a patient may note sudden onset of symptoms of severe anemia and jaundice over a few days.

Other patients exhibit episodic, acute hemolysis with hemoglobinuria induced by chilling. Increased unconjugated bilirubin is characteristic of hemolytic anemia.

An automatable format for accurate immunohematology testing by flow cytometry. A history of recent drug ingestion and absence of a significant cold agglutinin titer help to differentiate drug-induced immune hemolytic anemia from cold agglutinin disease. Am J Pediatr Hematol Oncol. Serologic findings in in autoimmune hemolytic anemia associated with immunoglobulin M warm autoantibodies.

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Autoimmune hemolytic anemia – Wikipedia

These classifications are based on the characteristics of the autoantibodies involved in the pathogenesis of the disease. Utility of adsorption techniques in serological evaluation of warm autoimmune haemolytic anaemia.

Cold agglutinin disease is treated with avoidance of cold exposure.

The cold agglutinin antibodies are not detected by the DAT because the cold agglutinins easily dissociate from the RBCs not only in vivo but also during the washing steps of the antiglobulin procedure.

New York, Churchill Livingstone, Even patients with severe hemolysis may have only mild splenomegaly.

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