Helpful Resources Introduction
Managing a practice is not always easy. Practices need payor information and billing forms. These are some of the tools that you will find in this section. Whether you have an established practice or you've just hung out your shingle, this information will help you and your staff.
CPT codes, descriptions and material only are copyright 2008 American Medical Association. All Rights Reserved. No fee schedules, basic units, relative values or related listings are included in CPT. The AMA assumes no liability for the data contained herein. Applicable FARS/DFARS Restrictions Apply to Government Use. PROCRIT Announcements Medicare Physician Fee Schedule Changes for 2009
PROCRIT Reimbursement - Overview
This PROCRIT Reimbursement - Overview outlines the key points you'll need to know for PROCRIT® (Epoetin alfa) reimbursement. Reference Guides to ICD-9-CM Diagnosis Codes
These separate Reference Guides for Oncology, Nephrology, Surgery and Virology contain the ICD-9 codes for PROCRIT. Oncology Toolkit
This Oncology Toolkit contains examples of the documents that are most often used to prepare a payment claim. You may find them helpful in developing, adding to, or modifying the material you currently use. Click here for a printable version
of the Evaluation & Management Progress Note and the Chemotherapy Treatment Notes/Flow Sheet. Full Prescribing Information, Including Boxed WARNINGS
For the package insert for PROCRIT® (Epoetin alfa) or for LEUSTATIN® (cladribine injection) click here:
Important Safety Information for PROCRIT® (Epoetin alfa)
WARNINGS: INCREASED MORTALITY, SERIOUS CARDIOVASCULAR EVENTS, THROMBOEMBOLIC EVENTS, STROKE and INCREASED RISK OF TUMOR PROGRESSION OR RECURRENCE
Chronic Renal Failure:
In clinical studies, patients experienced greater risks for death, serious cardiovascular events, and stroke when administered erythropoiesis-stimulating agents (ESAs) to target hemoglobin levels of 13 g/dL and above.
Individualize dosing to achieve and maintain hemoglobin levels within the range of 10 to 12 g/dL.
Cancer:
ESAs shortened overall survival and/or increased the risk of tumor progression or recurrence in some clinical studies in patients with breast, non-small cell lung, head and neck, lymphoid, and cervical cancers (see WARNINGS: Table 1).
To decrease these risks, as well as the risk of serious cardio- and thrombovascular events, use the lowest dose needed to avoid red blood cell transfusion.
Because of these risks, prescribers and hospitals must enroll in and comply with the ESA APPRISE Oncology Program to prescribe and/or dispense PROCRIT® to patients with cancer. To enroll in the ESA APPRISE Oncology Program, visit www.esa-apprise.com or call 1-866-284-8089 for further assistance.
Use ESAs only for treatment of anemia due to concomitant myelosuppressive chemotherapy.
ESAs are not indicated for patients receiving myelosuppressive therapy when the anticipated outcome is cure.
Discontinue following the completion of a chemotherapy course.
Perisurgery: PROCRIT® (Epoetin alfa) increased the rate of deep venous thromboses in patients not receiving prophylactic anticoagulation. Consider deep venous thrombosis prophylaxis.
(See WARNINGS: Increased Mortality, Serious Cardiovascular Events, Thromboembolic Events, and Stroke, WARNINGS: Increased Mortality and/or Increased Risk of Tumor Progression or Recurrence, INDICATIONS AND USAGE, and DOSAGE AND ADMINISTRATION.)
Patient Instructions for Use Instructions if you or your caregiver has been trained to give PROCRIT® injections at home.
Boxed WARNINGS: LEUSTATIN® (cladribine) Injection
LEUSTATIN (cladribine) Injection should be administered
under the supervision of a qualified physician
experienced in the use of antineoplastic therapy.
Suppression of bone marrow function should be anticipated.
This is usually reversible and appears to be
dose dependent. Serious neurological toxicity (including
irreversible paraparesis and quadraparesis) has
been reported in patients who received LEUSTATIN
Injection by continuous infusion at high doses (4 to 9
times the recommended dose for Hairy Cell Leukemia).
Neurologic toxicity appears to demonstrate a dose
relationship; however, severe neurological toxicity has
been reported rarely following treatment with standard
cladribine dosing regimens.
Acute nephrotoxicity has been observed with high
doses of LEUSTATIN (4 to 9 times the recommended
dose for Hairy Cell Leukemia), especially when given
concomitantly with other nephrotoxic agents/therapies.