Billing and Coding Guide - OTIPRIO — Get to know · PDF file · 2018-02-12Potential ICD-9-CM and ICD-10-PCS Procedure Codes ... Coverage and coding guidelines for OTIPRIO and its

Billing andCoding GuideEffective January 1, 2016

Please see Indication and Important Safety Information for OTIPRIO on page 4, and accompanying full Prescribing Information.

OTIPRIO™ (ciprofloxacin otic suspension) 6%

2Please see Indication and Important Safety Information for OTIPRIO on page 4, and accompanying full Prescribing Information.

Disclaimer

This guide is intended solely for educational purposes regarding possible codes that may be available for OTIPRIO. The information provided contains general reimbursement information only and represents Otonomy’s understanding of current reimbursement policies as of January 1, 2016. This coding and reimbursement information is subject to change and may become outdated. Information should not be construed as legal advice nor is it advice about how to code, complete, bill, or submit any particular claim for payment. It is important to check with the health plan directly to confirm coverage for individual patients. Information provided is not intended to increase or maximize reimbursement by any payer.

Otonomy disclaims any responsibility for claims submitted by providers or physicians. The information provided in this Guide is not a guarantee of coverage in any individual case. The key in all coding and billing to payers is to be truthful and not misleading, and to make full disclosures to the payer about the product and the procedures associated with its use when seeking reimbursement for any product or procedure. It is the provider’s and physician’s responsibility to determine appropriate codes, charges, and modifiers, and to submit bills for services and products consistent with what was rendered as well as the patient’s insurer requirements. Third-party payers may have different coverage and reimbursement policies and coding requirements. Such policies can change over time. Providers are encouraged to contact third-party payers for each patient to verify specific information on their coding policies.

3

Billing and Coding Guide


Contents

OTIPRIO Indication and Important Safety Information . . . . . . . . . . . . . . . . . . 4

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

Reimbursement Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

Private/Commercial . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

Medicaid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

Medicare . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

Coding for OTIPRIO . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

HCPCS Level II Codes for OTIPRIO . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

National Drug Code (NDC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Coding for Physician Administration Services . . . . . . . . . . . . . . . . . . . . . . . . . 8

Potential CPT® Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

Potential ICD-9-CM and ICD-10-PCS Procedure Codes . . . . . . . . . . . . . . 8

Coding for the Patient’s Disease/Condition . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

Potential ICD-9-CM and ICD-10-CM Diagnosis Codes . . . . . . . . . . . . . . . 9

Frequently Asked Questions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10


4

INDICATIONS AND USAGE

OTIPRIOTM (ciprofloxacin otic suspension) 6% is a fluoroquinolone antibacterial indicated for the treatment of pediatric patients with bilateral otitis media with effusion undergoing tympanostomy tube placement.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONSOTIPRIO is contraindicated in patients with a history of hypersensitivity to ciprofloxacin, to other quinolones, or to any of the components of OTIPRIO.

WARNINGS AND PRECAUTIONSPotential for Microbial Overgrowth: OTIPRIO may result in overgrowth of nonsusceptible bacteria and fungi. If such infections occur, institute alternative therapy.

ADVERSE REACTIONSAdverse reactions (incidence at least 3%) that occurred in two Phase 3 trials with OTIPRIO vs sham were: nasopharyngitis (5% vs 4%), irritability (5% vs 3%), and rhinorrhea (3% vs 2%).

USE IN SPECIFIC POPULATIONSPediatric Use: The safety and effectiveness of OTIPRIO in infants below six months of age have not been established.

Please see accompanying full Prescribing Information.

5



Introduction

Otonomy, Inc. has developed this reference guide to provide general billing and coding information related to OTIPRIO for physician and hospital billing staff when used in the ambulatory surgical center (ASC), hospital outpatient department (HOPD), or hospital inpatient setting. These materials are provided as information only. To assist you in preparing claims, this guide contains the following:

u Reimbursement Overview u Billing and Coding Information u Frequently Asked Questions (FAQs)

Reimbursement Overview

Coverage and coding guidelines for OTIPRIO and its administration will differ by insurer and are updated regularly. In addition, payment methodologies and rates may vary by insurer and are frequently dictated by the provider’s specific contract. It is a best practice to contact your patient’s health insurance company directly to ensure that you have the most recent local billing, coding, and coverage policy information, as well as answer any payment inquiries.

Codes allow healthcare providers to communicate with insurance companies to facilitate the reimbursement process and explain why the patient needed treatment, what drugs and services were provided, and where services were rendered. Coding guidelines may differ by insurer and are often updated regularly to reflect the addition and deletion of applicable codes. The following table provides an overview of the different codes and their description that may be applicable when billing for items and services related to OTIPRIO.

Code Set Description/Purpose

CPT®1 Codes (Level I HCPCS Codes)

Numeric coding system used to report medical services and procedures provided by healthcare professionals; includes CPT® E/M codes, which are numeric codes used to report office visit services provided by physicians

HCPCS Level II Codes Alpha-numeric coding system used to report specific drugs, supplies, and other healthcare equipment

ICD-9-CM/ICD-10-CM Diagnosis Codes

Numeric and alpha-numeric codes used to report diagnosis

ICD-9-CM/ICD-10-PCS Procedure Codes

Numeric and alpha-numeric codes used to report procedures, services, devices, and drugs in acute-care hospitals and other facility-based settings

NDC Numeric, universal, and unique 3-segment product identifier used to report human drugs

Revenue Codes Numeric codes used by hospitals to report services and supplies to specific cost centers

Legend

CPT®: Current Procedural TerminologyHCPCS: Healthcare Common Procedure Coding System

ICD-9-CM: International Classification of Diseases, 9th Revision, Clinical Modification

ICD-10-CM: International Classification of Diseases, 10th Revision, Clinical Modification

ICD-10-PCS: International Classification of Diseases, 10th Revision, Procedure Coding SystemNDC: National Drug Code

1 CPT® copyright 2014 American Medical Association. All rights reserved. CPT® is a registered trademark of the American Medical Association.



In addition, coverage and payment will also vary based on individual patient insurance details and provider contracts. An overview of the major insurer types is provided below.

Private/Commercial

Private insurance coverage policies for OTIPRIO and its administration may vary. Each private insurer determines its own coverage policies for drugs and procedures. In addition, most insurers offer multiple plans; coverage for procedures and/or drugs may vary depending on the details of that exact plan.

Medicaid

In general, state Medicaid programs will cover drugs for their FDA-approved indications. It will be important to understand your state Medicaid program’s specific coverage criteria for OTIPRIO and its administration as each state’s Medicaid agency determines its own coverage and payment policies. Medicaid recipients may also have the opportunity to enroll in managed care organizations (MCOs) offered in a particular state. Typically, Managed Medicaid guidelines for coverage are similar to private or commercial insurers and often vary by plan.

Medicare

Traditional Medicare consists of beneficiaries who receive their medical benefits through the following:

u �Medicare Part A: Inpatient services, hospitalizations, hospice care, skilled nursing facility stays, and some home health services

u ��Medicare Part B: Physician and outpatient services, durable medical equipment (DME), and some home health care, laboratory service

Currently, there is no Medicare national coverage determination (NCD) for OTIPRIO. As with most Part B covered drugs, local Medicare contractors have the discretion to develop local coverage determinations (LCDs) if necessary.

Regardless of the insurer type, formal published guidelines are typically developed for highly controversial or costly products and procedures; published policies regarding coverage for OTIPRIO may not be available. Contacting each patient’s insurance company to understand the specific guidelines for OTIPRIO is recommended.

7



Coding for OTIPRIO

Regardless of the setting of care in which the drug was administered, most payers require providers to list an HCPCS code and the NDC code on the claim form when billing for a particular drug.

HCPCS Level II Codes for OTIPRIO

Most payers recognize Healthcare Common Procedure Coding System (HCPCS) Level II national codes to identify and report drugs. Approved by the US Food and Drug Administration (FDA) on December 11, 2015, OTIPRIO has not yet been assigned a permanent, unique HCPCS code. Until a permanent code is assigned for OTIPRIO, payers may accept the following unclassified (miscellaneous) HCPCS codes:

Please consult payer-specific guidelines for the appropriate code to use for OTIPRIO to communicate which drug was provided and how much was administered.

National Drug Code (NDC)

The FDA and the manufacturer assign drugs/biologics a unique, 3-segment number, known as the National Drug Code (NDC). Many NDCs (including the one assigned to OTIPRIO) are displayed in a 10-digit format on the FDA-approved prescribing information. Proper billing for most payers or electronic data interchange systems requires that the NDC be submitted in the 11-digit numeric 5-4-2 format (ie, 55555-4444-22). Converting a 10-digit NDC to 11-digit format requires a strategically placed zero preceding the section that does not comply with the 5-4-2 format. Do not use hyphens when entering the actual data on your claim.

For example:

HCPCS Code Description

J3490 Unclassified drugs

C93992 Unclassified drugs or biologicals

10-Digit FormatOTIPRIO 10-Digit NDC

11-Digit FormatOTIPRIO 11-Digit NDC

Reporting on claim form

5-3-2 69251-201-01 5-4-2 69251-0201-01 69251020101

2 Note: C-codes are used for billing Medicare in the hospital outpatient setting. Please review private payer and Medicaid guidelines for your non-Medicare patients prior to utilizing the C-code to bill for OTIPRIO.



Coding for Physician Administration Services

Coding for the administration of OTIPRIO may vary depending on the setting of care. In the physician office, HOPD, and ASC, CPT® codes are used to describe procedures. In the hospital inpatient department, billers are required to use ICD-10-PCS codes to bill for procedures.

Potential CPT® Codes

Current Procedural Terminology (CPT®) codes are used to identify professional services (ie, drug administration). According to the CPT® instructions for use of the CPT® codebook, select the name of the procedure or service that accurately identifies the service performed. Do not select a CPT® code that merely approximates the service provided.

When provided during tube placement surgery, the administration of OTIPRIO is considered inclusive of the primary procedure and therefore not coded separately. Providers should use the appropriate tympanostomy CPT® code that best describes the services provided. Also, when performed bilaterally, report with modifier 50.

Potential ICD-9-CM and ICD-10-PCS Procedure Codes

ICD-9-CM and ICD-10-PCS codes are typically used to bill for procedures performed on inpatients. Effective October 1, 2015, all Health Insurance Portability and Accountability Act (HIPAA)-covered entities were required to transition from the ICD-9-CM coding system and bill procedures using ICD-10-PCS.

There is no category-specific code for drugs administered via intratympanic administration. Hospitals may therefore choose the code that best describes the procedure. Below is a list of the existing ICD-9-CM code and the ICD-10-PCS Crosswalk that may be applicable for describing the administration of OTIPRIO when administered during tube placement surgery.

CPT® Code Description

69433 Tympanostomy (requiring insertion of ventilating tube), local or topical anesthesia

69436 Tympanostomy (requiring insertion of ventilating tube), general anesthesia

ICD-9-CM Procedure Code ICD-10-PCS

20.94 Injection of tympanum

3E0B7GC Introduction of other therapeutic substance into ear, via natural or artificial opening

3E0B3GC Introduction of other therapeutic substance into ear, percutaneous approach

3E0BXGC Introduction of other therapeutic substance into ear, external approach

20.01 Myringotomy with insertion of tube

099500Z Drainage of right middle ear with drainage device, open approach

099600Z Drainage of left middle ear with drainage device, open approach

099770Z Drainage of right tympanic membrane with drainage device, via natural or artificial opening

099870Z Drainage of left tympanic membrane with drainage device, via natural or artificial opening

9



Coding for the Patient’s Disease/Condition

Potential ICD-9-CM and ICD-10-CM Diagnosis Codes

Effective October 1, 2015, all HIPAA-covered entities were required to transition from the ICD-9-CM coding system to ICD-10-CM.

ICD-10-CM diagnosis codes are used to report diseases and conditions and identify why a patient needs treatment. Guidelines for coding may differ by setting of care; therefore, it is important to reference the specific guidelines relevant to each individual patient encounter. Coding to the highest level of specificity may expedite the claims adjudication process. OTIPRIO is indicated for the treatment of pediatric patients with bilateral otitis media with effusion undergoing tympanostomy tube placement. The following ICD-9-CM diagnosis codes and the equivalent ICD-10-CM crosswalk below are examples of some codes that may be appropriate to describe a patient’s chief complaint.

Diagnosis Code System Code Description

ICD-9-CM 381.00 Acute nonsuppurative otitis media, unspecified

ICD-9-CM 382.00 Acute suppurative otitis media without spontaneous rupture of ear drum

ICD-10-CM H65.191–H65.199 Other acute nonsuppurative otitis

ICD-10-CM H66.001–H66.009 Acute suppurative otitis media without spontaneous rupture of ear drum



Frequently Asked Questions

Q1: What HCPCS code do I use to bill for OTIPRIO?

OTIPRIO currently does not have its own product code. In lieu of a specific code, insurers may accept unclassified drug codes to bill for new products, such as J3490 or C9399. Please contact the patient’s insurer to ensure proper coding for OTIPRIO.

Q2: What else do I need to know about coding OTIPRIO with an unclassified HCPCS drug code?

OTIPRIO was approved in 2015. Not all insurers will be familiar with OTIPRIO. Hence, the product may be billed using an unclassified drug code until OTIPRIO is assigned its own product-specific code.3 The patient’s insurer may need more information if they are unfamiliar with OTIPRIO; therefore, the provider’s billing staff should be prepared to submit the following information if requested: u Drug name (brand/generic)

u Route of administration

u Drug strength and dosage

u 11-digit National Drug Code (NDC)

u Customized letter of medical necessity

u Invoice

u FDA approval letter

u Package insert

u Chart notes

u Laboratory test results

u Patient medical history and documentation of medical necessity

u Prior therapies

u Supporting peer-reviewed medical journals and other clinical literature

Q3: What CPT® code do I use to bill for the administration of OTIPRIO in the ASC or HOPD?

When provided during tube placement surgery, the administration of OTIPRIO is considered inclusive of the primary procedure and therefore not coded separately. Providers should use the appropriate tympanostomy CPT® code (69433 or 69436) that best describes the services provided. Also, when performed bilaterally, report with modifier 50.

It is important to remember that insurers’ billing and coding guidelines may vary. Please contact the patient’s insurer to ensure proper coding for the administration of OTIPRIO.

3 Unclassified codes do not have “unit values” and are generally reported as “1 Unit” on the claim form or its electronic equivalent, regardless of the amount of drug administered. Check payer guidelines for appropriate reporting of units for an unclassified code.

11



Q4: How do I know if OTIPRIO is covered for my patient?

Formal published guidelines are typically developed for highly controversial or costly products and procedures; Otonomy does not anticipate that many payers will develop a formal policy regarding coverage for OTIPRIO. In general, it is a good rule of thumb to contact each payer to verify coverage parameters prior to the procedure.

Q5: What is the reimbursement for OTIPRIO?

Reimbursement for OTIPRIO and its administration will be based on the contracted arrangement between the provider and the payer. Please contact your patient’s insurer for specific information on payment rates and to understand how OTIPRIO and its administration are reimbursed.



For additional support or questions, please visit www.OTIPRIO.com or contact

[email protected].

©2016 Otonomy, Inc. All rights reserved. OTIPRIO is a trademark of Otonomy, Inc.

1-OTI16039

Please see Indication and Important Safety Information for OTIPRIOTM (ciprofloxacin otic suspension) on page 4, and accompanying full Prescribing Information.

HIGHLIGHTS OF PRESCRIBING INFORMATIONThese highlights do not include all the information needed to use OTIPRIO safely and effectively. See full prescribing information for OTIPRIO.

OTIPRIOTM (ciprofloxacin otic suspension), for intratympanic use

Initial U.S. Approval: 1987

---------------------------INDICATIONS AND USAGE--------------------------OTIPRIO is a fluoroquinolone antibacterial indicated for the treatment of pediatric patients with bilateral otitis media with effusion undergoing tympanostomy tube placement. (1)

-----------------------DOSAGE AND ADMINISTRATION----------------------· OTIPRIO is for intratympanic administration only. (2.1)

· OTIPRIO is intended for single-patient use with two 0.1 mL doses available in each vial. (2.1)

· Administer OTIPRIO as a single intratympanic administration of one 0.1 mL (6 mg) dose into each affected ear, following suctioning of the middle ear effusion. (2.1)

· See Full Prescribing Information for directions for OTIPRIO dose preparation. (2.2)

----------------------DOSAGE FORMS AND STRENGTHS--------------------Otic Suspension: Each OTIPRIO vial contains 1 mL of 6% (60 mg/mL) ciprofloxacin otic suspension. (3)

------------------------------CONTRAINDICATIONS---------------------------OTIPRIO is contraindicated in patients with a history of hypersensitivity to ciprofloxacin, to quinolones, or to any component of OTIPRIO. (4)

------------------------WARNINGS AND PRECAUTIONS----------------------Potential for Microbial Overgrowth: OTIPRIO may result in overgrowth of non-susceptible bacteria and fungi. (5.1)

------------------------------ADVERSE REACTIONS---------------------------The most frequently occurring adverse reactions (with an incidence rate greater than 3%) were nasopharyngitis and irritability. (6.1)

To report SUSPECTED ADVERSE REACTIONS, contact Otonomy at 1-800-826-6411 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

See 17 for PATIENT COUNSELING INFORMATION.

Revised: 12/2015

FULL PRESCRIBING INFORMATION: CONTENTS*

1 INDICATIONS AND USAGE2 DOSAGE AND ADMINISTRATION3 DOSAGE FORMS AND STRENGTHS4 CONTRAINDICATIONS5 WARNINGS AND PRECAUTIONS 5.1 Potential for Microbial Overgrowth6 ADVERSE REACTIONS8 USE IN SPECIFIC POPULATIONS 8.1 Pregnancy 8.2 Lactation 8.4 Pediatric Use

11 DESCRIPTION12 CLINICAL PHARMACOLOGY 12.1 Mechanism of Action 12.3 Pharmacokinetics 12.4 Microbiology13 NONCLINICAL TOXICOLOGY 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility 13.2 Animal Toxicology and/or Pharmacology14 CLINICAL STUDIES16 HOW SUPPLIED/STORAGE AND HANDLING17 PATIENT COUNSELING INFORMATION

*Sections or subsections omitted from the full prescribing information are not listed.

1

FULL PRESCRIBING INFORMATION

1 INDICATIONS AND USAGEOTIPRIO is indicated for the treatment of pediatric patients with bilateral otitis media with effusion undergoing tympanostomy tube placement.

2 DOSAGE AND ADMINISTRATION

2.1 Dosage and Important Administration Instructions· OTIPRIO is for intratympanic administration only.· OTIPRIO is intended for single-patient use, discard unused portion.· Administer OTIPRIO as a single intratympanic administration of one 0.1 mL (6 mg) dose into each affected ear, following suctioning of middle ear effusion.

2.2 Preparation of OTIPRIODirections for OTIPRIO dose preparation and handling is illustrated in Figure 1 below.

Figure 1: Directions for OTIPRIO Dose Preparation

3 DOSAGE FORMS AND STRENGTHSOtic Suspension: Each 1 mL of OTIPRIO contains a white, preservative-free, sterile otic suspension consisting of 6% (60 mg/mL) ciprofloxacin in a single-patient use glass vial.

4 CONTRAINDICATIONSOTIPRIO is contraindicated in patients with a history of hypersensitivity to ciprofloxacin, to other quinolones, or to any of the components of OTIPRIO.

5 WARNINGS AND PRECAUTIONS

5.1 Potential for Microbial Overgrowth OTIPRIO may result in overgrowth of nonsusceptible bacteria and fungi. If such infections occur, institute alternative therapy.

6 ADVERSE REACTIONS

6.1 Clinical Trials ExperienceBecause clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect the rates observed in practice.In two randomized, sham-controlled Phase 3 clinical trials, 530 pediatric patients with bilateral otitis media with effusion undergoing tympanostomy tube placement were treated with OTIPRIO or sham administered intra-operatively as a single dose. The median age of the pediatric patients enrolled in the clinical trials was 1.5 years; 62% of patients were 6 months through 2 years of age and 38% of patients were greater than 2 years of age. Adverse reactions that occurred in at least 3% of OTIPRIO patients and at an incidence greater than sham are presented in Table 1.

Table 1: Adverse Reactions in Phase 3 Trials

Adverse Reactions OTIPRIO(N=357)

Sham(N=173)

Nasopharyngitis 5% 4%Irritability 5% 3%Rhinorrhea 3% 2%

8 USE IN SPECIFIC POPULATIONS

8.1 Pregnancy

Risk SummaryAnimal reproduction studies have not been conducted with OTIPRIO. No adequate and well-controlled studies have been performed in pregnant women. Because of the negligible systemic exposure associated with clinical administration of OTIPRIO, this product is expected to be of minimal risk for maternal and fetal toxicity when administered to pregnant women.

8.2 Lactation

Risk SummaryCiprofloxacin is excreted in human milk with systemic administration. However, because of the negligible systemic exposure after otic application, nursing infants of mothers receiving OTIPRIO should not be affected.

8.4 Pediatric UseThe safety and effectiveness of OTIPRIO in infants below six months of age have not been established.The safety and effectiveness of OTIPRIO was established in 530 pediatric patients with bilateral otitis media with middle ear effusion undergoing myringotomy with tympanostomy tube placement. The median age of patients enrolled in the clinical trials was 1.5 years; 62% of patients were 6 months through 2 years of age and 38% of patients were greater than 2 years of age [see Adverse Reactions (6.1) and Clinical Studies (14)].

11 DESCRIPTIONOTIPRIO (ciprofloxacin otic suspension) 6% contains the synthetic fluoroquinolone antibacterial, ciprofloxacin. OTIPRIO is for intratympanic administration. OTIPRIO is supplied as a white, preservative-free, sterile otic suspension of 6% (w/v) ciprofloxacin in a neutral pH, buffered, isotonic solution in a single-patient use glass vial with a rubber stopper containing 1 mL. The inactive ingredients are poloxamer 407, sodium chloride, tromethamine, hydrochloric acid and water for injection (WFI).The thermosensitive suspension exists as a liquid at room temperature or below and gels when warmed [see How Supplied/Storage and Handling (16)].

2

STEP 1 PreparationMaterials needed:

1 vial of OTIPRIO (enough for 2 doses); Two 1 mL luer lock syringes; Two 18G-21G preparation needles; Two 20-24G, 2-3 inch blunt, flexible administration needles; Alcohol pads; Optional: ice pack and drape to keep OTIPRIO vial coldKeep product cold during preparation. If OTIPRIO thickens during preparation, place the vial back in refrigeration.

STEP 2 OTIPRIO MixingTo keep the vial cold during shaking, hold the OTIPRIO vial by the aluminum seal to prevent gelation. Shake the vial for 5 to 8 seconds to mix well until a visually homogenous suspension is obtained.Always hold the vial by the aluminum seal to prevent gelation.

STEP 3 OTIPRIO RemovalUsing an 18-21G needle, withdraw 0.3 mL of the suspension into the 1 mL syringe.

STEP 4 Replace with the Administration NeedleReplace the needle with a 20-24G, 2-3 inch blunt, flexible needle to be used for administration.

STEP 5 Priming the SyringePrime the needle leaving a dose of 0.1 mL (0.1 cc).

STEP 6 Preparing Second Dose for Bilateral Administration OnlyRepeat Steps 3, 4, and 5 using the same vial to prepare a second syringe for the other ear and dispose of the vial.Use a different syringe for each ear.After preparation, syringes can be kept at room temperature or in the refrigerator prior to administration.Keep syringes on their side.Discard syringes if not administered in 3 hours.

Ciprofloxacin has the following nomenclature: 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid. Its empirical formula is C17H18FN3O3 and its molecular weight is 331.3.Its chemical structure is as follows:

Figure 2: Structure of Ciprofloxacin

12 CLINICAL PHARMACOLOGY

12.1 Mechanism of ActionCiprofloxacin is a fluoroquinolone antibacterial [see Microbiology (12.4)].

12.3 PharmacokineticsThe plasma concentration of ciprofloxacin following bilateral administration of 0.1 mL OTIPRIO was not measured.

12.4 Microbiology

Mechanism of ActionThe bactericidal action of ciprofloxacin results from interference with the enzyme DNA gyrase, which is needed for the synthesis of bacterial DNA.

ResistanceBacterial resistance to fluoroquinolones can develop through chromosomally- or plasmid-mediated mechanisms. In vitro studies demonstrated cross-resistance between ciprofloxacin and some fluoroquinolones. There is generally no cross- resistance between ciprofloxacin and other classes of antibacterial agents, such as beta-lactams or aminoglycosides.

Antimicrobial ActivityCiprofloxacin has been shown to be active against most isolates of the following bacteria: Gram-positive Bacteria Staphylococcus aureus Streptococcus pneumoniae Gram-negative Bacteria Haemophilus influenzae Moraxella catarrhalis Pseudomonas aeruginosa

13 NONCLINICAL TOXICOLOGY

13.1 Carcinogenesis, Mutagenesis, Impairment of FertilityEight in vitro mutagenicity tests have been conducted with ciprofloxacin, and the test results are listed below: Salmonella/Microsome Test (Negative) Escherichia coli DNA Repair Assay (Negative) Mouse Lymphoma Cell Forward Mutation Assay (Positive) Chinese Hamster V79 Cell HGPRT Test (Negative) Syrian Hamster Embryo Cell Transformation Assay (Negative) Saccharomyces cerevisiae Point Mutation Assay (Negative) Saccharomyces cerevisiae Mitotic Crossover and Gene Conversion Assay (Negative) Rat Hepatocyte DNA Repair Assay (Positive)

Thus, 2 of the 8 in vitro tests were positive, but results of the following 3 in vivo test systems gave negative results: Rat Hepatocyte DNA Repair Assay Micronucleus Test (Mice) Dominant Lethal Test (Mice)

Long-term carcinogenicity studies in mice and rats have been completed for ciprofloxacin. After daily oral doses of 750 mg/kg in mice and 250 mg/kg in rats (for mice and rats respectively, approximately 300 and 200 times the maximum recommended clinical dose of ototopical ciprofloxacin based upon body surface area, assuming total absorption of ciprofloxacin from the ear of a patient treated with OTIPRIO) were administered for up to 2 years, there was no evidence that ciprofloxacin had any carcinogenic or tumorigenic effects in these species.

Fertility studies performed in rats at oral doses of ciprofloxacin up to 100 mg/kg/day revealed no evidence of impairment. This would be approximately 80 times the maximum recommended clinical dose of ototopical ciprofloxacin based upon body surface area, assuming total absorption of ciprofloxacin from the ear of a patient treated with OTIPRIO.

13.2 Animal Toxicology and/or PharmacologyGuinea pigs dosed in the middle ear with OTIPRIO exhibited no drug-related structural or functional changes of the cochlear hair cells.

14 CLINICAL STUDIESTwo randomized, multicenter, controlled clinical trials in 532 pediatric patients with bilateral otitis media with effusion undergoing myringotomy with tympanostomy tube placement evaluated the safety and efficacy of OTIPRIO when administered intra-operatively as a single dose. The median age of patients enrolled in the clinical trials was 1.5 years; 62% of patients were 6 months through 2 years of age and 38% of patients were greater than 2 years of age. The efficacy endpoint for both trials was the cumulative proportion of study treatment failures through Day 15, defined as the occurrence of any of the following events: otorrhea as determined by a blinded assessor on or after 3 days post-surgery, otic or systemic antibacterial drug use for any reason any time post-surgery, as well as patients who missed visits or were lost-to-follow-up. Table 2 presents the results from each Phase 3 trial.

Table 2: Cumulative Proportion of Treatment Failures Through Day 15 in Phase 3 Trials

Trial 1 (N=266) Trial 2 (N=266)

OTIPRIO ShamDifference(Sham – OTIPRIO)(95% CI)

OTIPRIO ShamDifference(Sham – OTIPRIO)(95% CI)

Treatment Failure 25%(44/179)

45% (39/87)

20%(8%, 32%)2

21%(38/178)

45%(40/88)

24%(12%, 36%)2

Reason for Failure1

Otorrhea 7% 11% 7% 27%

Otic antibacterial drugs 6% 17% 5% 8%

Systemic antibacterial drugs 2% 5% 3% 3%

Lost-to-follow-up and missed visit 10% 11% 6% 7%

1 the earliest occurring treatment failure event, and patients were classified as a treatment failure due only to that component for the remainder of the study

2 P-value <0.001 for Cochran-Mantel-Haenszel test (adjusted for age-group)

Administration of OTIPRIO did not lead to impairment in hearing function, middle ear function or tube patency by Day 29.

16 HOW SUPPLIED/STORAGE AND HANDLINGOTIPRIO is a sterile, preservative-free, otic suspension of 6% (60 mg/mL, w/v) ciprofloxacin in a neutral pH buffered, isotonic solution containing poloxamer 407. Each OTIPRIO carton contains 1 mL of 6% (60 mg/mL, w/v) ciprofloxacin in a 2 mL single-patient use glass vial fitted with a rubber stopper. (NDC-69251-201-01) OTIPRIO should be stored at 2 to 8°C (36 to 46°F) until prior to use to prevent thickening during preparation. Protect from light. Store in the original carton until dose preparation.

17 PATIENT COUNSELING INFORMATIONAdvise patients and their caregiver(s) that there may be drainage from the ear the first few days following ear tube surgery, but if the ear becomes painful, or continuous ear discharge is noted, or the patient develops a fever, advise patients and their caregiver(s) to consult their physician.

Distributed by:Otonomy, Inc.San Diego, CA 92121www.otiprio.comOTIPRIOTM is a Trademark of Otonomy.

U.S. Patent Nos: 8,318,817 and 9,205,048

1-OTI15193

3

Documents

Billing and Coding Guide - OTIPRIO — Get to know · PDF file · 2018-02-12Potential ICD-9-CM and ICD-10-PCS Procedure Codes ... Coverage and coding guidelines for OTIPRIO and its