This is the American ICD-10-CM version of D57.0 - other international versions of ICD-10 D57.0 may differ. Applicable To. Sickle-cell disease with crisis. Hb-SS disease with vasoocclusive pain. The following code (s) above D57.0 contain annotation back-references. Annotation Back-References.
Broad term used to describe several different acute conditions occurring with sickle cell disease, including aplastic crisis, hemolytic crisis, and vasoocclusive crisis. ICD-10-CM D57.00 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0): 811 Red blood cell disorders with mcc 812 Red blood cell disorders without mcc
2018/2019 ICD-10-CM Diagnosis Code D57.419. Sickle-cell thalassemia with crisis, unspecified. 2016 2017 2018 2019 Billable/Specific Code. D57.419 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Hb-SS disease with acute chest syndrome. 2016 2017 2018 2019 2020 Billable/Specific Code. D57.01 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM D57.01 became effective on October 1, 2019.
D57. 00 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. 00 became effective on October 1, 2021.
A vaso-occlusive crisis occurs when the microcirculation is obstructed by sickled RBCs, causing ischemic injury to the organ supplied and resultant pain.
ICD-10 code D57. 00 for Hb-SS disease with crisis, unspecified 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 .
ICD-10-CM Code for Sickle-cell disorders D57.
Diagnosis. Diagnosis of vaso-occlusive crisis is based on clinical manifestations, complete blood count with white blood cell differential, platelet count, reticulocyte count, and comprehensive metabolic panel with liver and kidney function tests.
Four major types of crises are recognised in sickle cell anaemia: aplastic, acute sequestration, hyper-haemolytic, and vaso-occlusive crises.
A sickle cell crisis is pain that can begin suddenly and last several hours to several days. It happens when sickled red blood cells block small blood vessels that carry blood to your bones. You might have pain in your back, knees, legs, arms, chest or stomach. The pain can be throbbing, sharp, dull or stabbing.
SymptomsAnemia. Sickle cells break apart easily and die. ... Episodes of pain. Periodic episodes of extreme pain, called pain crises, are a major symptom of sickle cell anemia. ... Swelling of hands and feet. ... Frequent infections. ... Delayed growth or puberty. ... Vision problems.
Hemoglobin sickle C disease is a “mild" form of sickle cell anemia. Your child's red blood cells (RBC's) contain two abnormal hemoglobins called hemoglobin S and hemoglobin C. Hemoglobin is the substance in the RBC's which carries oxygen to all parts of the body.
9: Fever, unspecified.
V78. 2 - Screening for sickle-cell disease or trait | ICD-10-CM.
Test Details If Sickle Cell Screen is positive, then Hemoglobinopathy Evaluation will be performed at an additional charge (CPT code(s): 83020). Hemoglobinopathy Evaluation includes: Hemoglobin A1, Fetal Hemoglobin, Hemoglobin A2, and any hemoglobin variants.