Hereditary deficiency of other clotting factors
ICD-10 D68.2 is a billable code used to indicate a diagnosis of hereditary deficiency of other clotting factors.
Hereditary deficiency of other clotting factors refers to a group of genetic disorders characterized by the inadequate production or dysfunction of specific clotting factors that are essential for normal blood coagulation. These deficiencies can lead to a range of bleeding disorders, which may manifest as easy bruising, prolonged bleeding after injury or surgery, and spontaneous bleeding episodes. Unlike hemophilia A and B, which are deficiencies of factor VIII and IX respectively, hereditary deficiencies of other clotting factors can involve factors such as factor XI, factor VII, and others. The severity of bleeding symptoms can vary widely among individuals, depending on the specific factor involved and the degree of deficiency. Diagnosis typically involves a combination of clinical evaluation, family history, and laboratory tests, including coagulation factor assays. Management may include factor replacement therapy, desmopressin for certain deficiencies, and supportive care to prevent and control bleeding episodes. Understanding the genetic basis of these conditions is crucial for effective management and genetic counseling.
Detailed documentation of coagulation studies, family history, and clinical symptoms.
Patients presenting with unexplained bleeding, family history of bleeding disorders, or abnormal coagulation test results.
Ensure that all relevant laboratory tests are documented to support the diagnosis.
Genetic testing results, family pedigree, and counseling notes.
Patients undergoing genetic testing for hereditary bleeding disorders.
Document the specific genetic mutations identified to support the diagnosis.
Used to confirm the specific factor deficiency in patients suspected of having hereditary bleeding disorders.
Document the specific factors tested and the results.
Hematology specialists should ensure that all relevant factors are assessed.
D68.2 refers specifically to hereditary deficiencies of clotting factors other than factors VIII and IX, while D66 is used for hemophilia A, which is a deficiency of factor VIII.
Ensure that the specific factor deficiency is clearly stated in the medical record, along with any relevant laboratory results and clinical symptoms.
