Hereditary Factor II Deficiency (Prothrombin) | Medical Algorithm

Are you evaluating a patient with a bleeding disorder?

Yes

Age of the patient

years

Gender

Male

Female

Are there siblings or other family members with a similar bleeding disorder?

Yes

Does the patient have?

• easy bruisability?

Yes

• epistaxis?

Yes

• soft tissue bleeding and/or hematomas?

Yes

• bleeding after surgery or trauma?

Yes

• menorrhagia?

Yes

• post-partum bleeding?

Yes

• hemarthroses?

Yes

• intracerebral hemorrhage?

Yes

• a prolonged PT?

Yes

• a prolonged aPTT?

Yes

• a prolonged thrombin time?

Yes

• decreased prothrombin activity?

Yes

• decreased prothrombin antigen?

Yes

Results

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Results Interpretation and Description References Next Steps

Data complete?

Evaluation appropriate?

Is there evidence of a hereditary disorder?

Number of clinical findings for a bleeding disorder

Number of laboratory findings that can be seen in a prothrombin deficiency

Is there evidence of for a hereditary deficiency in prothrombin?

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Interpretation and Description

References

Next Steps in Evaluation

Diagnosis

Clinical Diagnosis, Including Family History For Genetics
- Clinical Findings in a Patient with an Hereditary Deficiency of Factor XII
Laboratory Tests
Other Testing
- Correction of a Coagulation Factor Deficiency By Liver Transplantation
Criteria For Diagnosis
Complications
- Indications for Screening a Patient with Hemophilia A for a Factor VIII Inhibitor
- Coagulation Factor Deficiency Following Liver Transplantation

Therapy

Options
- Perioperative Management of a Patient with Hereditary Deficiency of Factor XII
Selection
- Indications for Screening a Patient with Hemophilia A for a Factor VIII Inhibitor
- Correction of a Coagulation Factor Deficiency By Liver Transplantation
Administration

Monitoring

Response To Therapy
- Titer of VIII Inhibitor and Response to Factor VIII Replacement in Hemophilia A

Evaluation

Results

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Power Your Solutions with 5,000+ Automated Medical Analytics

Interpretation and Description

References

Next Steps in Evaluation

Diagnosis

Therapy

Monitoring

Specialty

Objective

ICD-10

Clinical Findings in Patient with Hereditary Deficiency of Factor II (Prothrombin)

Purpose: To evaluate a patient with a bleeding disorder for evidence of a hereditary deficiency of prothrombin (Factor II).

Evaluation

Results

Please fill out required fields.

MedicalAlgorithms.com APIs

Power Your Solutions with 5,000+ Automated Medical Analytics

Interpretation and Description

References

Next Steps in Evaluation

Diagnosis

Therapy

Monitoring

Specialty

Objective

ICD-10