2018/2019 ICD-10-CM Diagnosis Code D59.9. Acquired hemolytic anemia, unspecified. 2016 2017 2018 2019 Billable/Specific Code. D59.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Diagnosis Index entries containing back-references to D59.9: Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9 ICD-10-CM Diagnosis Code D64.9. Anemia, unspecified 2016 2017 2018 2019 2020 Billable/Specific Code Hemoglobinemia D59.9 Icteroanemia, hemolytic (acquired) D59.9
D58.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM D58.9 became effective on October 1, 2018. This is the American ICD-10-CM version of D58.9 - other international versions of ICD-10 D58.9 may differ.
Hereditary hemolytic anemia, unspecified. Includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (rh) disease of newborn.
The destruction of red blood cells is called hemolysis. Red blood cells carry oxygen to all parts of your body. If you have a lower than normal amount of red blood cells, you have anemia. When you have anemia, your blood can't bring enough oxygen to all your tissues and organs.
Hemolytic anemia is defined by the premature destruction of red blood cells, and can be chronic or life-threatening. It should be part of the differential diagnosis for any normocytic or macrocytic anemia. Hemolysis may occur intravascularly, extravascularly in the reticuloendothelial system, or both.
Hemolytic anemia is a blood disorder that typically happens when your red blood cells break down or die faster than your body can replace them with new blood cells. People may develop hemolytic anemia by inheriting genetic conditions that cause anemia, certain infections and certain medications.
For this test, your doctor removes a small amount of bone marrow tissue through a needle. The tissue is examined to check the number and type of cells in the bone marrow. You may not need bone marrow tests if blood tests show what's causing your hemolytic anemia.
The breakdown of red blood cellsListen to pronunciation. (hee-MAH-lih-sis) The breakdown of red blood cells. Some diseases, medicines, and toxins may cause red blood cells to break down more quickly than usual.
Hemolysis is the breakdown of red blood cells, which can have an effect on laboratory results. Serum samples containing more than 100 mg/dL of hemoglobin can cause non-specific binding in serologic tests. Therefore, serologic testing is not recommended for a serum sample containing more than this amount of hemoglobin.
TypesAlpha-hemolysis.Beta-hemolysis.Gamma-hemolysis.
One cause of hemolysis is the action of hemolysins, toxins that are produced by certain pathogenic bacteria or fungi. Another cause is intense physical exercise. Hemolysins damage the red blood cell's cytoplasmic membrane, causing lysis and eventually cell death....HemolysisCausesOsmosis4 more rows
Causes of hemolysisHemolysis can be caused by:Shaking the tube too hard.Using a needle that is too small.Pulling back too hard on a syringe plunger.Pushing on a syringe plunger too hard when expelling blood into a collection device.
While hemolysis can be a lifelong asymptomatic condition, it most often presents as anemia when erythrocytosis cannot match the pace of red cell destruction. Hemolysis also can manifest as jaundice, cholelithiasis, or isolated reticulocytosis.
Hemolysis may falsely increase the following analytes: AST, alanine transaminase (ALT), LDH, total bilirubin, glucose, calcium, phosphorus, total protein, albumin, magnesium, amylase, lipase, creatine kinase (CK), iron, hemoglobin, and mean corpuscular hemoglobin concentration (MCHC).
One cause of hemolysis is the action of hemolysins, toxins that are produced by certain pathogenic bacteria or fungi. Another cause is intense physical exercise. Hemolysins damage the red blood cell's cytoplasmic membrane, causing lysis and eventually cell death....HemolysisCausesOsmosis4 more rows
TypesAlpha-hemolysis.Beta-hemolysis.Gamma-hemolysis.
Hemolysis may occur in vitro or in vivo. In vitro hemolysis can result from the lysis of the red blood cells during collection and handling of the blood sample. In vivo hemolysis occurs if the rate of erythrocyte destruction is increased, thereby decreasing erythrocyte life span.
Your health care provider may recommend this test if you have signs or symptoms of paroxysmal nocturnal hemoglobinuria (PNH) or hemolytic anemia of unknown cause. Hemolytic anemia is a condition in which red blood cells die before they should.
The 2022 edition of ICD-10-CM D59.10 became effective on October 1, 2021.
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Clinical Information. A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies. Hemolytic anemia due to various intrinsic defects of the erythrocyte.
The 2022 edition of ICD-10-CM D58.9 became effective on October 1, 2021.
Other symptoms of warm antibody hemolytic anemia include yellowing of the skin and whites of the eyes (jaundice) and enlargement of the spleen (splenomegaly).
Warm antibody hemolytic anemia is the most common form of autoimmune hemolytic anemia. It is defined by the presence of autoantibodies that destroy red blood cells at temperatures equal to or greater than normal body temperature (37 degrees Celsius).
Patients with cold antibody hemolytic anemia experience weakness, dizziness, fatigue, headache, ringing in the ears (tinnitus), and spots before the eyes. In some cases, affected individuals may experience sweating and coldness of the fingers and/or toes and uneven bluish or reddish discoloration of the skin of the digits, ankles, and wrists (acrocyanosis or Raynaud’s sign).