2018/2019 ICD-10-CM Diagnosis Code D57.412. Sickle-cell thalassemia with splenic sequestration. D57.412 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Sickle-cell thalassemia with splenic sequestration. D57.412 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Sickle-cell thalassemia with acute chest syndrome. D57.411 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 D57.411 became effective on October 1, 2018.
Diagnosis Index entries containing back-references to D57.40: Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9 ICD-10-CM Diagnosis Code D64.9 Disease, diseased - see also Syndrome sickle-cell D57.1 ICD-10-CM Diagnosis Code D57.1 Hemoglobinopathy (mixed) D58.2 ICD-10-CM Diagnosis Code D58.2
289.52 - Splenic sequestration. ICD-10-CM.
ICD-10 code D57. 4 for Sickle-cell thalassemia is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .
Splenic sequestration (blood trapped in the spleen) refers to a sudden condition of pooling of large amounts of blood in the spleen. Children with sickle cell disease between ages five months and two years represent most cases of splenic sequestration.
V78. 2 - Screening for sickle-cell disease or trait | ICD-10-CM.
Overview. Sickle beta thalassemia is an inherited condition that affects hemoglobin, the protein in red blood cells that carries oxygen to different parts of the body. It is a type of sickle cell disease.
Sickle-cell disease without crisis D57. 1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D57. 1 became effective on October 1, 2021.
In sickle cell disease, acute splenic sequestration can happen at any age, but normally it occurs in infants and young children. Acute splenic sequestration happens when sickled red blood cells get trapped in the spleen, causing the spleen to enlarge.
Splenic sequestration is a potentially life-threatening condition that's most commonly seen as a complication of sickle cell disease (SCD). It happens mostly in children. The condition causes a child's spleen to get bigger and lowers the amount of oxygen-carrying red blood cells in their body.
Young children with sickle cell anemia are at risk for acute splenic sequestration crises. These occur when an excessive amount of blood becomes trapped in the spleen, causing a dangerous drop in the circulating blood volume.
D56. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
9.
Sickle cell trait (SCT) is not a disease, but having it means that a person has inherited the sickle cell gene from one of his or her parents. People with SCT usually do not have any of the symptoms of sickle cell disease (SCD) and live a normal life.
Anemia, also spelt anaemia, is usually defined as a decrease in the amount of red blood cells (RBCs) or hemoglobin in the blood. It can also be defined as a lowered ability of the blood to carry oxygen.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D57.412. Click on any term below to browse the alphabetical index.
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code D57.412 and a single ICD9 code, 289.52 is an approximate match for comparison and conversion purposes.