URINE DRUG TESTING FOR SUBSTANCE ABUSE TREATMENT AND CHRONIC PAIN MANAGEMENT

Similar documents
ALLERGY TESTING AND TREATMENT

CRYOABLATION OF SOLID TUMORS

PERCUTANEOUS FACET JOINT DENERVATION

POSITRON EMISSION TOMOGRAPHY (PET)

VENTRICULAR ASSIST DEVICES AND TOTAL ARTIFICIAL HEARTS

OSTEOCHONDRAL ALLOGRAFTS AND AUTOGRAFTS IN THE TREATMENT OF FOCAL ARTICULAR CARTILAGE LESIONS

FEP Medical Policy Manual

ADVANCED THERAPIES FOR PHARMACOLOGICAL TREATMENT OF PULMONARY HYPERTENSION

Corporate Medical Policy

ORTHOGNATHIC SURGERY

PNEUMATIC COMPRESSION DEVICES IN THE HOME SETTING

Payment Policy: Urine Specimen Validity Testing Reference Number: CC.PP.056 Product Types: ALL Effective Date: 11/01/2017 Last Review Date:

Drug Testing Policy. Reimbursement Policy CMS Approved By. Policy Number. Annual Approval Date. Reimbursement Policy Oversight Committee

MEDICAL POLICY Drug Testing

Urine Drug Testing In Pain Management and Substance Abuse Treatment Corporate Medical Policy

DRUG TESTING POLICY. Policy Number: ADMINISTRATIVE T0 Effective Date: October 1, Related Policies None

Drug Testing Policy. Approved By 05/10/2017. Application This reimbursement policy applies to UnitedHealthcare Community Plan Medicaid products.

DRUG TESTING POLICY. Policy Number: ADMINISTRATIVE T0 Effective Date: March 1, Related Policies None

DRUG TESTING POLICY. Policy Number: ADMINISTRATIVE T0 Effective Date: January 1, Related Policies None

MEDICAL POLICY No R2 DRUG TESTING

Drug Testing Policy. Reimbursement Policy CMS Approved By. Policy Number. Annual Approval Date. Reimbursement Policy Oversight Committee

Drug Testing Policy. Approved By 06/14/2017

MEDICAL POLICY Drug Testing

Drug Testing in Pain Management and Substance Use Disorder Treatment

2017 Drug Screen Tests

Medical Policy. MP Drug Testing in Pain Management and Substance Use Disorder Treatment

Payment Policy Drug Testing EFFECTIVE DATE: POLICY LAST UPDATED:

Clinical Policy: Outpatient Testing for Drugs of Abuse

Medical Affairs Policy

B. To assess an individual when clinical evaluation suggests use of non-prescribed medications or illegal substances; or

DRUG TESTING IN PAIN MANAGEMENT AND SUBSTANCE USE DISORDER(S) TREATMENT

Based on our criteria and assessment of the peer-reviewed literature, presumptive (immunoassay) in office or pointof-care

Clinical Policy: Outpatient Testing for Drugs of Abuse Reference Number: CP.MP.HN 542

Clinical Policy: DNA Analysis of Stool to Screen for Colorectal Cancer

Urinary Metabolite Tests for Adherence to Direct-Acting Antiviral Medications for Hepatitis C Archived Medical Policy

Clinical Policy: Outpatient Testing for Drugs of Abuse Reference Number: PA.CP.MP.50

Clinical Policy: Atezolizumab (Tecentriq) Reference Number: CP.PHAR.235 Effective Date: 06/16 Last Review Date: 05/17

Quality ID #414: Evaluation or Interview for Risk of Opioid Misuse National Quality Strategy Domain: Effective Clinical Care

GENETIC TESTING AND COUNSELING FOR HERITABLE DISORDERS

Clinical Policy: Naltrexone (Vivitrol) Reference Number: CP.PHAR.96 Effective Date: Last Review Date: Line of Business: Medicaid

Clinical Policy: Naltrexone (Vivitrol) Reference Number: CP.PHAR.96 Effective Date: Last Review Date: Line of Business: Medicaid

Clinical Policy: Outpatient Testing for Drugs of Abuse Reference Number: PA.CP.MP.50

Clinical Policy: Implantable Miniature Telescope for Age Related Macular Degeneration Reference Number: CP.MP.517

DENOMINATOR: All patients 18 and older prescribed opiates for longer than six weeks duration

Medical Policy Outpatient Drug Screening and Testing. No Prior Authorization X X

Corporate Medical Policy

Medical Policy. Urine Drug Screening. Policy Number: Policy History

Protocol. Drug Testing in Pain Management and Substance Abuse Treatment

Local Coverage Article for Chiropractic Services (A47798) Contractor Information. Article Information. Contractor Name. Contractor Numbers

CLINICAL POLICY Clinical Policy: Extended Release Opioid Analgesics

OPIOID PRESCRIBING RULES

Clinical Policy: Buprenorphine-Naloxone (Bunavail, Suboxone, Zubsolv) Reference Number: CP.PMN.81 Effective Date: Last Review Date: 02.

See Important Reminder at the end of this policy for important regulatory and legal information.

URINE DRUG TOXICOLOGY

Readopt with amendment Med 502, effective (Document #11090), to read as follows:

Clinical Policy: Cochlear Implant Replacements

Pharmacogenomic Testing for Warfarin Response (NCD 90.1)

2019 COLLECTION TYPE: MIPS CLINICAL QUALITY MEASURES (CQMS) MEASURE TYPE: Process High Priority

Clinical Policy: Digital Breast Tomosynthesis Reference Number: CP.MP.90

FEP Medical Policy Manual

Linking Opioid Treatment in Primary Care. Roxanne Lewin M.D.

Clinical Policy: Fecal Calprotectin Assay Reference Number: CP.MP.135

Clinical Policy: Robotic Surgery Reference Number: CP.MP. 207

Clinical Policy: Cochlear Implant Replacements Reference Number: CP.MP.14

Clinical Policy: Multiple Sleep Latency Testing

Electrical Stimulation Device Used for Cancer Treatment

Clinical Policy: Opioid Analgesics Reference Number: CP.PMN.97 Effective Date: Last Review Date: 02.19

Disclosures. Get Your Specimens in Order:

COMMUNITY-BASED SUBSTANCE USE DISORDER FEE SCHEDULE (eff May 15, 2017)

Clinical Policy: Opioid Analgesics Reference Number: CP.PMN.97 Effective Date: Last Review Date: 02.18

See Important Reminder at the end of this policy for important regulatory and legal information.

COMMUNITY-BASED SUBSTANCE USE DISORDER FEE SCHEDULE (eff Aug 1, 2017)

80305, 80306, 80307,G0480, G0481, G0482, G0483, G0659

See Important Reminder at the end of this policy for important regulatory and legal information.

Clinical Policy: Desmopressin Acetate (DDAVP Injection) Reference Number: CP.PHAR.214

Analysis of Human DNA in Stool Samples as a Technique for Colorectal Cancer Screening

2018 OPTIONS FOR INDIVIDUAL MEASURES: REGISTRY ONLY. MEASURE TYPE: Outcome

Proposed Revision to Med (i)

Clinical Policy: Dabrafenib (Tafinlar) Reference Number: CP.PHAR.239 Effective Date: 07/16 Last Review Date: 07/17 Line of Business: Medicaid

Clinical Policy: Aflibercept (Eylea) Reference Number: CP.PHAR.184

Sympathetic Electrical Stimulation Therapy for Chronic Pain

Clinical Policy: Homocysteine Testing Reference Number: CP.MP.121

COMMUNITY-BASED SUBSTANCE USE DISORDER FEE SCHEDULE (eff Aug 1, 2017)

2018 Drug Screening Code Updates for WV Medicaid

Urine Drug Testing for Substance Use and Pain Management

Report to the Social Services Appropriations Subcommittee

Medication Assisted Treatment: Buprenorphine Clinical Coverage Policy 8A-3 Amended Date: 10/1/2015 DRAFT Table of Contents

Ultrasound and Fluoroscopic Paravertebral Facet Joint Injections

Genetic Testing for Inherited Conditions

Claim Submission. Agenda 1/31/2013. Payment Basics

Clinical Policy: EEG in the Evaluation of Headache Reference Number: CP.MP.155

Clinical Policy: Ferric Carboxymaltose (Injectafer) Reference Number: CP.PHAR.234

COMMUNITY-BASED SUBSTANCE USE DISORDER FEE SCHEDULE (eff July 1, 2017)

Addiction and Recovery Treatment Services (ARTS) Reimbursement Structure

Clinical Policy: Laser Therapy for Skin Conditions Reference Number: CP.MP.123 Last Review Date: 08/17

SAMPLE. Behavioral Health Services

Rule Governing the Prescribing of Opioids for Pain

Nutrient/Nutritional Panel Testing

Clinical UM Guideline

Clinical Policy: Total Artificial Heart Reference Number: CP.MP.127

Transcription:

Status Active Medical and Behavioral Health Policy Section: Laboratory Policy Number: VI-47 Effective Date: 07/21/2014 Blue Cross and Blue Shield of Minnesota medical policies do not imply that members should not receive specific services based on the recommendation of their provider. These policies govern coverage and not clinical practice. Providers are responsible for medical advice and treatment of patients. Members with specific health care needs should consult an appropriate health care professional. URINE DRUG TESTING FOR SUBSTANCE ABUSE TREATMENT CHRONIC PAIN MANAGEMENT Description: Urine drug testing (UDT) is a method used for monitoring patients in substance abuse treatment and pain management programs who may use non-prescribed drugs or misuse prescribed drugs, such as opioids. Advantages of UDT are that it is readily available, and standardized techniques for detecting drugs in urine exist. Patients are often assessed by UDT before starting treatment and monitored while they are receiving treatment. The two major categories of UDT are qualitative drug testing and quantitative drug testing. Qualitative tests are immunoassay tests that provide a positive or negative result for the presence of one or more drugs or drug classes based on a prespecified threshold, but do not indicate specific levels. These tests can be performed either in a laboratory or at point-of-care and generally have rapid turnaround time. Quantitative tests are able to quantify the amount of drug or metabolite present and are used to confirm the presence of a specific drug identified by a screening test. These tests can also be used to identify drugs that cannot be measured by immunoassays, such as certain synthetic or semisynthetic opioids. Quantitative (i.e., confirmatory) tests are performed in a laboratory and gas chromatography/mass spectrometry is considered to be the criterion standard. Laboratory tests must meet the general regulatory standards of the Clinical Laboratory Improvement Amendments (CLIA). Certain pointof-care immunoassays are commercially available as CLIA-waived tests for drugs such as cocaine, methadone, morphine, and oxycodone. Note: This policy addresses use of UDT in outpatient substance abuse treatment or outpatient chronic pain management settings only. Definitions: Stabilization phase: The stabilization and/or detoxification phase of

treatment is for patients who experience withdrawal symptoms following prolonged drug abuse. This phase focuses on finding a medication dosage that will minimize withdrawal symptoms and cravings and decrease or eliminate drug abuse. Most patients in opioid treatment are expected to be on a stable dose of medication within 4 weeks of initiating treatment. Maintenance phase: The maintenance and/or rehabilitation phase of treatment follows the stabilization phase of treatment. This phase begins when a patient is responding optimally to medication treatment and routine dosage adjustments are no longer needed. For most patients in opioid treatment, targeted qualitative screening once every 1 to 3 months is sufficient during the maintenance phase of treatment. Policy: I. Qualitative Urine Drug Testing A. Qualitative urine drug testing for substance abuse treatment may be considered MEDICALLY NECESSARY under any of the following conditions: 1. On initial entrance into a substance abuse treatment program when all of the following criteria are met: a. An adequate clinical assessment of patient history and risk of substance abuse is performed, including obtaining information from the state prescription drug monitoring program; b. Clinicians have knowledge of test interpretation; c. Clinical documentation specifies how the test result will be used to guide clinical decision making. 2. During the stabilization phase of treatment no more frequently than once a week for a maximum of 4 weeks. 3. During the maintenance phase of treatment no more frequently than once a month. B. Qualitative urine drug testing for chronic pain management may be considered MEDICALLY NECESSARY under any of the following conditions: 1. On initial entrance into a chronic pain management program when all of the following criteria are met: a. An adequate clinical assessment of patient history and risk of substance abuse is performed, including obtaining information from the state prescription drug monitoring program; b. Clinicians have knowledge of test interpretation; c. Clinical documentation specifies how the test result will be used to guide clinical decision making. 2. During subsequent monitoring of treatment no more frequently than the following times according to the risk level of the individual, as determined by a validated screening tool for assessing the risk of aberrant drugrelated behaviors (e.g., the Opioid Risk Tool [ORT] or the Screener and Opioid Assessment for Patients with Pain Revised [SOAPP-R]): a. Twice a year for patients who are low or moderate risk;

b. Four times a year for patients who are high risk OR receiving an opioid dose >120 mg MED/d; c. At the time of the office visit for patients demonstrating aberrant behavior defined by one or more of the following: i. Lost prescriptions; ii. Requests for early refills; iii. Obtained opioids from multiple providers; iv. Unauthorized dose escalation; v. Apparent intoxication. C. Qualitative urine drug testing is considered NOT MEDICALLY NECESSARY in all other situations, including but not limited to routine testing and testing for non-medical purposes. II. Quantitative Urine Drug Testing A. Quantitative urine drug testing for substance abuse treatment or chronic pain management may be considered MEDICALLY NECESSARY when ALL of the following criteria are met: 1. Qualitative urine drug testing was performed according to the medically necessary criteria described in section I; 2. The result of qualitative urine drug testing was one or more of the following: a. Positive for a non-prescribed drug with abuse potential; OR b. Positive for an illicit drug (e.g., methamphetamine or cocaine); OR c. Negative for prescribed medications; 3. Clinical documentation specifies supporting rationale for each quantitative test ordered; 4. Clinical documentation specifies how the test result will be used to guide clinical decision making. B. Quantitative urine drug testing for substance abuse treatment or chronic pain management may be considered MEDICALLY NECESSARY when BOTH of the following criteria are met: 1. A qualitative test for the relevant drug(s) is not commercially available; 2. The testing is performed according to the medically necessary criteria described in section I, with the exception that it is quantitative rather than qualitative testing. C. Quantitative urine drug testing is considered NOT MEDICALLY NECESSARY in all other situations, including but not limited to routine testing and testing for non-medical purposes. Coverage: Blue Cross and Blue Shield of Minnesota medical policies apply generally to all Blue Cross and Blue Plus plans and products. Benefit plans vary in coverage and some plans may not provide coverage for certain services addressed in the medical policies.

Medicaid products and some self-insured plans may have additional policies and prior authorization requirements. Receipt of benefits is subject to all terms and conditions of the member s summary plan description (SPD). As applicable, review the provisions relating to a specific coverage determination, including exclusions and limitations. Blue Cross reserves the right to revise, update and/or add to its medical policies at any time without notice. For Medicare NCD and/or Medicare LCD, please consult CMS or National Government Services websites. Refer to the Pre-Certification/Pre-Authorization section of the Medical Behavioral Health Policy Manual for the full list of services, procedures, prescription drugs, and medical devices that require Precertification/Pre-Authorization. Note that services with specific coverage criteria may be reviewed retrospectively to determine if criteria are being met. Retrospective denial of claims may result if criteria are not met. Coding: The following codes are included below for informational purposes only, and are subject to change without notice. Inclusion or exclusion of a code does not constitute or imply member coverage or provider reimbursement. CPT: 80100 Drug screen, qualitative; multiple drug classes chromatographic method, each procedure 80101 Drug screen, qualitative; single drug class method (eg, immunoassay, enzyme assay), each drug class 80102 Drug confirmation, each procedure 80103 Tissue preparation for drug analysis 80104 Drug screen, qualitative; multiple drug classes other than chromatographic method, each procedure 80150-80299 Quantitative Drug Testing Therapeutic Drug Assay Code Range 82000-84999 Quantitative Drug Testing Chemistry Code Range HCPCS: G0431 Drug screen, qualitative; multiple drug classes by high complexity test method (e.g., immunoassay, enzyme assay), per patient encounter G0434 Drug screen, other than chromatographic; any number of drug classes, by CLIA waived test or moderate complexity test, per patient encounter Policy History: Developed May 14, 2014

Cross Reference: Current Procedural Terminology (CPT ) is copyright 2013 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. Copyright 2014 Blue Cross Blue Shield of Minnesota.