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How To Use HCPCS Code C1721

HCPCS code C1721 describes a specific medical device known as a cardioverter-defibrillator, dual chamber (implantable). This code is used to identify and bill for the insertion and implantation of this device, which is used to treat certain heart conditions. In this article, we will explore the details of HCPCS code C1721, including its official description, procedure, when to use it, billing guidelines, historical information, Medicare and insurance coverage, and provide examples of when this code should be billed.

1. What is HCPCS C1721?

HCPCS code C1721 is used to identify the specific medical device known as a cardioverter-defibrillator, dual chamber (implantable). This device is designed to monitor and regulate the heart’s rhythm, delivering electrical shocks when necessary to restore a normal heartbeat. It is typically implanted in patients who have a high risk of life-threatening arrhythmias or sudden cardiac arrest.

2. Official Description

The official description of HCPCS code C1721 is “Cardioverter-defibrillator, dual chamber (implantable)”. The short description is “Enteral supp not otherwise c”. This description accurately reflects the purpose and nature of the device.

3. Procedure

  1. The procedure for implanting a cardioverter-defibrillator, dual chamber (implantable) involves several steps:
  • Preparation: The patient is prepared for the procedure, which may involve administering anesthesia and sterilizing the surgical site.
  • Incision: The surgeon makes an incision in the chest to access the heart.
  • Lead Placement: Leads, which are thin wires, are inserted into the heart through blood vessels. These leads are connected to the cardioverter-defibrillator device.
  • Device Implantation: The cardioverter-defibrillator device is implanted in a pocket created under the skin, typically near the collarbone.
  • Testing and Programming: Once the device is implanted, it is tested to ensure proper functioning and programmed to meet the patient’s specific needs.
  • Closure: The incision is closed using sutures or staples, and the surgical site is dressed and bandaged.

4. When to use HCPCS code C1721

HCPCS code C1721 should be used when a healthcare provider performs the insertion and implantation of a cardioverter-defibrillator, dual chamber (implantable) device. This code is specifically for the device itself and does not cover any additional services or supplies that may be necessary during the procedure.

5. Billing Guidelines and Documentation Requirements

When billing for HCPCS code C1721, healthcare providers should ensure that the documentation supports the medical necessity of the procedure and includes the following information:

  • Procedure notes describing the insertion and implantation of the cardioverter-defibrillator device
  • Details of any complications or additional procedures performed
  • Documentation of the patient’s medical history and diagnosis supporting the need for the device
  • Any relevant pre- and post-operative care provided

6. Historical Information and Code Maintenance

HCPCS code C1721 was added to the Healthcare Common Procedure Coding System on January 01, 1985. It has an effective date of January 01, 1996. There have been no maintenance actions taken for this code, as indicated by the action code N, which means no maintenance for this code.

7. Medicare and Insurance Coverage

HCPCS code C1721 is eligible for coverage by Medicare and other insurance providers. The pricing indicator code 57 indicates that the device is priced by other carriers, and the multiple pricing indicator code A indicates that it is not applicable as HCPCS priced under one methodology. Healthcare providers should consult the Medicare Carriers Manual Reference Section Number 2130 for specific guidelines and instructions on billing and reimbursement for this code.

8. Examples

Here are five examples of scenarios in which HCPCS code C1721 should be billed:

  1. A 65-year-old patient with a history of ventricular arrhythmias undergoes the insertion and implantation of a cardioverter-defibrillator, dual chamber (implantable) device to manage their condition.
  2. A 50-year-old patient with a previous cardiac arrest receives a cardioverter-defibrillator, dual chamber (implantable) device to prevent future life-threatening arrhythmias.
  3. A 45-year-old patient with a congenital heart defect undergoes the insertion and implantation of a cardioverter-defibrillator, dual chamber (implantable) device to manage their condition and reduce the risk of sudden cardiac arrest.
  4. A 70-year-old patient with heart failure and a high risk of arrhythmias receives a cardioverter-defibrillator, dual chamber (implantable) device as part of their treatment plan.
  5. A 55-year-old patient with a history of ventricular tachycardia undergoes the insertion and implantation of a cardioverter-defibrillator, dual chamber (implantable) device to monitor and regulate their heart rhythm.

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