ICD-10 Code D59.32 | Hereditary hemolytic-uremic syndrome Symptoms, Diagnosis, Billing

Hereditary hemolytic-uremic syndrome is a rare genetic disorder characterized by the triad of hemolytic anemia, acute renal failure, and thrombocytopenia. It is caused by mutations affecting the regulation of the complement system, leading to excessive activation and subsequent damage to the kidneys and red blood cells. Accurate coding with ICD-10 Code D59.32 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate care and resources.

What is ICD-10 Code D59.32 for Hereditary hemolytic-uremic syndrome?

ICD-10 Code D59.32 specifically denotes hereditary hemolytic-uremic syndrome, a condition that arises from genetic mutations affecting the complement system. This code should be utilized in clinical documentation and billing when diagnosing patients with this syndrome, particularly when they present with symptoms such as hemolytic anemia, renal impairment, and low platelet counts.

ICD-10 Code D59.32 – Clinical Definition and Explanation of Hereditary hemolytic-uremic syndrome

Hereditary hemolytic-uremic syndrome is primarily caused by genetic mutations that lead to dysregulation of the complement system, resulting in hemolysis, renal failure, and thrombocytopenia. The condition requires prompt medical attention due to its potential for severe complications, including chronic kidney disease.

Key Clinical Features:

• Hemolytic anemia characterized by fatigue, pallor, and jaundice.
• Acute renal failure presenting with oliguria or anuria.
• Thrombocytopenia leading to increased bleeding risk.
• Elevated serum creatinine and blood urea nitrogen (BUN) levels.
• Family history of similar symptoms or genetic predisposition.

ICD-10 Code D59.32 for Hereditary hemolytic-uremic syndrome – SOAP Notes & Clinical Use

ICD-10 Code D59.32 is utilized in SOAP notes to document the clinical presentation, assessment, and treatment of patients with hereditary hemolytic-uremic syndrome. This code aids in capturing the severity of the condition and informs both acute and chronic care management strategies.

What Does ICD-10 Code D59.32 for Hereditary hemolytic-uremic syndrome Mean in SOAP Notes?

In SOAP notes, ICD-10 Code D59.32 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of hereditary hemolytic-uremic syndrome. This ensures continuity of care, supports accurate billing, and meets EHR documentation standards.

Treatment Options for ICD-10 Code D59.32 – Hereditary hemolytic-uremic syndrome

Hereditary hemolytic-uremic syndrome often necessitates hospitalization for management of acute symptoms and complications. Treatment focuses on addressing the underlying genetic issues and supportive care.

Antibiotic Therapy:

• Not applicable as this condition is not infectious.

Supportive Care:

• Fluid management to prevent dehydration and support renal function.
• Transfusion of red blood cells for severe anemia.
• Platelet transfusions if significant bleeding occurs.
• Renal replacement therapy (dialysis) if acute renal failure is present.

Infection Control:

• Standard precautions to prevent secondary infections during hospitalization.

How to Document Symptoms of Hereditary hemolytic-uremic syndrome (ICD-10 D59.32) in SOAP Notes

Subjective:

• Patient reports fatigue and pallor over the past week.
• History of jaundice and dark urine noted.
• Complaints of easy bruising and bleeding gums.
• Family history of similar symptoms in relatives.

Objective:

• Vital signs: BP 110/70 mmHg, HR 88 bpm, Temp 98.6°F.
• Physical exam reveals pallor and mild jaundice.
• Laboratory results: Hemoglobin 8 g/dL, Platelets 50,000/mm³, Creatinine 2.5 mg/dL.
• Urinalysis shows hematuria and proteinuria.

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SOAP Note Guidelines for Diagnosing Hereditary hemolytic-uremic syndrome (ICD-10 Code D59.32)

Assessment:

• Diagnosis: Hereditary hemolytic-uremic syndrome, moderate severity.
• ICD-10 Code: D59.32.
• Triggers: Genetic mutation affecting complement regulation.
• Complications: Risk of chronic kidney disease.

Plan:

• Initiate fluid resuscitation and monitor renal function.
• Administer blood transfusions as needed for anemia.
• Consult nephrology for potential dialysis.
• Educate patient on disease management and genetic counseling.

Treatment & Plan Section for ICD-10 Code D59.32 – Hereditary hemolytic-uremic syndrome

• Transfusion of red blood cells for symptomatic anemia.
• Fluid management to maintain renal perfusion.
• Monitoring of renal function and electrolytes.
• Patient education on recognizing symptoms of complications.

Using ICD-10 Code D59.32 for Hereditary hemolytic-uremic syndrome in Billing & SOAP Note Compliance

• Ensure accurate documentation of symptoms and clinical findings in Subjective (S) and Objective (O) sections.
• Utilize D59.32 for billing when hereditary hemolytic-uremic syndrome is diagnosed.
• Align treatment plans with clinical guidelines to support justified billing.
• Document any relevant comorbidities or complications for comprehensive coding.

Related ICD-10 Codes Often Used with Hereditary hemolytic-uremic syndrome

• D59.31 – Acquired hemolytic anemia

ICD-10 Code D59.32 in Medical Billing and Insurance for Hereditary hemolytic-uremic syndrome

ICD-10 Code D59.32 is crucial for billing in hospital, ER, or infectious disease care settings, ensuring accurate reimbursement for services rendered.

Billing Notes:

• Document all relevant clinical findings and treatments to support the ICD-10 claim.
• Use D59.32 in conjunction with other codes for comprehensive billing.
• Ensure that the diagnosis is clearly linked to the services provided in the medical record.
• Review payer-specific guidelines for any additional documentation requirements.

Common CPT Pairings: