Summary & Overview
HCPCS C1717: HDR Brachytherapy Iridium-192 Source
HCPCS Level II code C1717 denotes a non-stranded, high dose rate iridium-192 brachytherapy source billed per source. These radioactive sources are central to HDR brachytherapy treatments used across oncology to deliver localized, high-dose radiation with rapid dose falloff, reducing exposure to surrounding healthy tissue. Nationally, accurate coding for brachytherapy sources matters for clinical documentation, radiation safety compliance, and consistent payment processing for institutional and physician services.
Key payers covered in this overview include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise explanation of the code's clinical role, typical sites of service such as hospital outpatient departments and radiation oncology clinics, and the kinds of materials and supply charges this code represents. The publication summarizes common billing considerations, typical modifiers that may appear on claims (provided in the input), and related administrative issues affecting reimbursement and claim adjudication.
This summary provides benchmarks and policy context relevant to facility billing for HDR brachytherapy supplies, highlights areas where coding clarity supports compliance, and outlines the clinical context for use of C1717. Data not available in the input is noted where applicable in the full publication.
Billing Code Overview
HCPCS Level II code C1717 represents a brachytherapy source, non-stranded, high dose rate iridium-192, per source. This item is a disposable radioactive source used in high-dose-rate (HDR) brachytherapy procedures, in which a high-activity Ir-192 source is temporarily placed within or next to a tumor to deliver concentrated radiation.
Service type: Brachytherapy source supply for HDR brachytherapy procedures
Typical site of service: Hospital outpatient departments, radiation oncology clinics, and ambulatory surgery centers where HDR brachytherapy is performed
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult undergoing high-dose-rate (HDR) brachytherapy for a localized malignancy such as gynecologic (cervical or endometrial) cancer, prostate cancer, or selected head and neck or soft-tissue tumors. The patient is evaluated by a radiation oncologist and multidisciplinary team; imaging (MRI/CT) and clinical exam determine target volumes. On the day of treatment the patient is brought to the radiation oncology suite or operating room; applicable anesthesia or sedation may be provided. Interstitial or intracavitary applicators are placed and connected to a remote afterloader. Individual C1717 sources (non-stranded, Iridium-192) are loaded into the afterloader per treatment plan; each source is billed per source as indicated. Post-treatment, applicators are removed and the patient is observed for immediate complications before discharge or transfer to inpatient care.
Key workflow steps:
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Referral and consultation with radiation oncology.
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Simulation and treatment planning with CT/MRI and brachytherapy planning software.
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Applicator placement under anesthesia or sedation in procedure area or operating room.
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Source loading with
C1717Ir-192 high-dose-rate non-stranded sources into the afterloader for planned dwell positions and times. -
Delivery of HDR fractions per protocol, source removal, and post-procedure monitoring.
Typical site of service: outpatient radiation oncology department, specialized brachytherapy suite, or operating room when combined with surgical procedures.
Typical patient scenario: a 62-year-old female with locally advanced cervical cancer receives external beam radiotherapy followed by HDR intracavitary brachytherapy; during each HDR fraction the treatment team loads multiple non-stranded Iridium-192 sources into the afterloader according to the planned dwell pattern and documents the number of sources used for billing per source.