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June 2019

All Providers

New care management program to launch in 2020

Blue Cross Blue Shield of Michigan is preparing to launch an all-new integrated care management program next year.

The new program takes a holistic, member-centric approach to help ensure the greatest effect on our members’ overall health and the cost of care. It will be deployed across all lines of business, including Blue Cross PPO, Blue Care Network, group and individual customers, and Medicare Advantage members.

It’s not intended to replace the doctor-patient relationship in any way, but to support health care providers in their efforts to provide the best possible care for patients. Keep in mind that the Provider-Delivered Care Management program, which is part of Value Partnerships, will continue.

For more details, see the column by Drs. Aaron Friedkin and Duane DiFranco and Ann Baker in the May ‑ June 2019 issue of Hospital and Physician Update.


Gain insights about your patients from CAHPS research on improving the patient experience

The Centers for Medicare & Medicaid Services can help providers better understand their Medicare patients’ needs and expectations through information gleaned from the Consumer Assessment of Healthcare Providers and Systems, or CAHPS, survey.

CMS annually compiles survey findings as part of an effort to improve the patient experience and better understand health outcomes. Results from the CAHPS survey, developed by the Agency for Healthcare Research and Quality, contribute to the CMS star ratings system.

You can learn more about the CAHPS survey and how the survey can be used to improve the patient experience by clicking here. Also, be sure to check out the CAHPS survey tip sheet to find out why this annual survey is so important, how it’s conducted, what questions are asked and ways you can address care opportunities for patients.


SCIO Health Analytics auditing outpatient claims for commercial business

SCIO Health Analytics®, an independent company that provides services for Blue Cross Blue Shield of Michigan, began auditing outpatient claims for our commercial business on May 1, 2019.

The audits will:

  • Start with claims paid on or after Jan. 1, 2018.
  • Confirm compliance with Blue Cross guidelines and policy.
  • Validate proper billing of revenue, CPT and HCPCS codes, modifiers and units.
  • Ensure services are documented.
  • Detect, prevent and correct waste and abuse.
  • Facilitate accurate claims payments.

You’ll need to provide the proper medical charts for review. After an audit, SCIO will send you its findings and instructions for appeal, if necessary.

If you need to speak to a SCIO representative during the audit, call 1-866-628-3488, ext. 7525.


Battling the opioid epidemic: A roundup of recent news and information

Most Americans think drug companies should be held responsible for their role in opioid crisis
A new NPR poll found that 57% of Americans say pharmaceutical companies should be held responsible for making the opioid crisis worse. Additionally, it found that a third of Americans have been touched directly by the deadly opioid epidemic that kills more than 100 people every day. One in three have been personally affected in some way, either by knowing someone who has overdosed or by knowing someone with an opioid addiction, said Mallory Newall, lead Ipsos researcher on the survey. To read more, click here.**

Opioid company’s top executives found guilty of bribing doctors
A federal jury in Boston found John Kapoor, founder of Insys Therapeutics, and four other executives guilty of bribing doctors to boost sales of Subsys®, a highly addictive fentanyl sublingual spray, npr.org** reported.

Forum addresses role employers can play in stemming opioid epidemic
The human costs of the opioid epidemic are substantial, and they trickle down to employers in the form of absenteeism and compromised performance on the job. One study found that opioid abuse costs U.S. employers $18 billion annually in lost productivity. Blue Cross Blue Shield of Michigan recently sponsored a Health Forum of West Michigan panel discussion about opioids. It looked at five key steps employers need to take to help employees struggling with substance use disorders. Read more in a MI Blues Perspectives blog.

Meijer launches drug take-back program
Meijer recently announced a Consumer Drug Take-Back Program at all its supercenters across the Midwest. At Meijer, you can simply dispose of your old prescriptions during pharmacy hours at secure kiosks. This includes opioids, controlled substances and over-the-counter medications. The Meijer Drug Take-Back Program allows our customers to remove the risk of an unforeseen accident occurring with expired or unused medications, while enabling them to properly dispose of prescription drugs and reducing the possibility of creating a public health hazard, said Jason Beauch, vice president of Meijer Pharmacy. Read more in a MI Blues Perspectives blog.

What if patients don’t want to be prescribed opioids?
With so many people becoming addicted to opioids over the past few years, it’s not surprising that many people don’t want to rely on opioids to relieve pain. Dr. Duane DiFranco, vice president, Medicare STARs and Clinical Performance, offers some nonopioid alternatives in a MI Blues Perspectives blog targeted to members.

**Blue Cross Blue Shield of Michigan doesn't own or control this website.


HCPCS update: New codes added

The Centers for Medicare & Medicaid Services recently added several new codes as part of its quarterly Health Care Procedure Coding System updates. The codes, effective date and Blue Cross Blue Shield of Michigan’s coverage decisions are below.

Outpatient prospective payment system — Injections

Code Change Coverage comments Effective date
C9040 Added Covered for facility only April 1, 2019
C9041 Added Covered for facility only April 1, 2019
C9042 Added Covered for facility only April 1, 2019
C9043 Added Covered for facility only April 1, 2019
C9044 Added Covered for facility only April 1, 2019
C9045 Added Covered for facility only April 1, 2019
C9046 Added Covered for facility only April 1, 2019
C9141 Added Covered for facility only April 1, 2019

None of the information included in this article is intended to be legal advice and, as such, it remains the provider’s responsibility to ensure that all coding and documentation are done in accordance with all applicable state and federal laws and regulations.


Billing chart: Blues highlight medical, benefit policy changes

You’ll find the latest information about procedure codes and Blue Cross Blue Shield of Michigan billing guidelines in the following chart.

This billing chart is organized numerically by procedure code. Newly approved procedures will appear under the New Payable Procedures heading. Procedures for which we have changed a billing guideline or added a new payable group will appear under Updates to Payable Procedures. Procedures for which we are clarifying our guidelines will appear under Policy Clarifications. New procedures that are not covered will appear under Experimental Procedures.

You will also see that descriptions for the codes are no longer included. This is a result of recent negotiations with the AMA on use of the codes.

We will publish information about new BCBS groups or changes to group benefits under the Group Benefit Changes heading.

For more detailed descriptions of the BCBSM policies for these procedures, please check under the Medical/Payment Policy tab in Explainer on web-DENIS. To access this online information:

  • Log in to web-DENIS.
  • Click on BCBSM Provider Publications & Resources.
  • Click on Benefit Policy for a Code.
  • Click on Topic.
  • Under Topic Criteria, click on the drop-down arrow next to Choose Identifier Type and then click on HCPCS Code.
  • Enter the procedure code.
  • Click on Finish.
  • Click on Search.
Code* BCBSM changes to:
Basic Benefit and Medical Policy, Group
Variations Payment Policy, Guidelines
NEW PAYABLE PROCEDURES

0501T, 0502T, 0503T, 0504T, 75574**

**Covered starting Jan. 1, 2010

Noninvasive fractional flow reserve

The use of noninvasive fractional flow reserve to guide decisions about the use of invasive coronary angiography in select patients has been established. It’s a useful diagnostic option when indicated, effective Jan. 1, 2019.

Payment policy
Modifiers 26 and TC don’t apply to procedure codes 0501T, 0502T, 0503T and 0504T. They also aren’t subject to the Radiology Management Program, although 75574 is. Procedure codes 0501T and 0504T aren’t covered in a facility location.

Inclusions:
Patients must meet both criteria:

  • Have stable chest pain
  • Have intermediate risk of coronary artery disease (e.g., suspected or presumed stable ischemic heart disease)

And meet one of the following:

  • Diagnosis of congestive heart failure/cardiomyopathy/left ventricular dysfunction when all the following are met:
    • Left ventricular ejection fraction < 55%
    • Low to moderate coronary heart disease riska
    • Coronary artery disease hasn’t been excluded as the etiology of the cardiomyopathy
  • Symptomaticb or asymptomatic patients undergoing non‑coronary surgery (including open and percutaneous valvular procedures or ascending aortic surgery)
    • All the pre-operative information can be obtained using cardiac CT, and
    • Moderate coronary heart disease riska
  • Symptomaticb patients who are suspected of having coronary artery disease and meet one of the following:
    • During a planned outpatient exercise stress test (without imaging), all the following apply:
      • Performed within the past 60 days
      • Patient is symptomaticb
      • During the test, one of the following occurred:
        • Exercise-induced chest pain
        • ST segment change
        • Abnormal blood pressure response
        • Complex ventricular arrhythmias
    • Have undergone either myocardial perfusion imaging or a stress echocardiogram within the past 60 days and imaging is one of the following:
      • Neither normal or abnormal
      • Abnormal
    • No coronary artery disease imaging (e.g., myocardial perfusion imaging, cardiac PET scan, stress echo or coronary angiogram) has been performed within the preceding 60 days.
  • Symptomaticb patient with abnormal resting EKG
    • Exercise stress test (without imaging) would be uninterpretable related to one of the following:
      • Left bundle branch block
      • Paced ventricular rhythm
      • Left ventricular hypertrophy with repolarization abnormalities
      • Resting ST segment depression
        • ≥ 1 mm
      • Digoxin effects as evidence by one of the following:
        • ST depression in a concave shape
        • Flattened, inverted or biphasic T waves
        • Shortened QT interval
      • Pre-excitation syndrome (e.g., Lown-Ganong-Levine syndrome, Wolff-Parkinson-White syndrome)
        • Short PR interval (< 0.12 sec)

Note: Fractional flow reserve using coronary tomography angiography requires at least a 64-slice coronary computed tomography angiography and can’t be calculated when images lack sufficient quality.

a Risk factor is determined using standard assessment methods (e.g., SCORE, or Systematic Coronary Risk Evaluation, chart)
b Symptomatic is defined by one or more of the following:

  • Chest pain with low probability of coronary artery disease, but high risk
  • Moderate to high risk of coronary artery disease and one of the following:
    • Chest, jaw, neck, shoulder, arm, hand, epigastric or back pain
    • Diaphoresis
    • Syncope
    • Shortness of breath
  • High risk of coronary artery disease and one of the following:
    • Palpitations
    • Lightheadedness
    • Near syncope
    • Nausea or vomiting
    • Anxiety
    • Weakness
    • Fatigue
  • Patients with any cardiac symptom who have any of the following diseases associated with coronary artery disease:
    • Abdominal aortic aneurysm
    • Chronic renal insufficiency or renal failure
    • Diabetes mellitus
    • Established and symptomatic peripheral vascular disease
    • History of:
      • Cerebrovascular accident
      • Transient ischemic attack
      • Carotid endarterectomy
      • High-grade carotid stenosis (>70%)

Exclusions:

  • Assessment of coronary arteries for suspected congenital anomalies
  • Patients who have:
    • Body mass index > 35% kg/m2
    • Presence of uncontrolled rapid heart rate or arrhythmia
    • Suspicion of acute coronary syndrome when acute myocardial infarction or unstable angina hasn’t been ruled out.
    • History of:
      • Myocardial infarction within the last 30 days
      • Coronary artery bypass graft surgery
      • Presence of dense arterial calcification or intracoronary stent
      • Evidence of clinical instability (e.g., unstable blood pressure – systolic < 90 mmHg, severe congestive heart failure, acute pulmonary edema, cardiogenic shock)
  • Patients who require emergent procedures
  • Patients not meeting inclusionary guidelines

J3490
J3590

Basic benefit and medical policy

Tegsedi (inotersen)

Tegsedi (inotersen) is considered established, effective Oct. 5, 2018.

Tegsedi (inotersen) is covered when all the following criteria are met:

  • Age 18 or older
  • Must have a diagnosis of peripheral nerve disease caused by hereditary transthyretin-mediated amyloidosis, or hTTR, with documented transthyretin, or TTR, mutation
  • Documentation of clinical signs and symptoms of peripheral neuropathy or autonomic neuropathy
  • Must have polyneuropathy disability, or PND, score ≤ IIIb
  • Must have baseline FAP Stage 1 or 2
  • Must not be on concomitant treatment with Tegsedi and Onpattro

Quantity limit: FDA-approved dosing
Initial authorization period: One year

FDA approved indication and diagnosis:
For treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR) in adults

Dosing and administration
Dosing: 284 mg administered subcutaneously once weekly.

Tegsedi (inotersen) isn’t a benefit for URMBT.

Prior authorization is required for this drug.

NDCs: 71860-0007-01, 71860-0007-02

J9999

Basic benefit and medical policy

Libtayo (cemiplimab-rwlc)

Effective Sept. 28, 2018, Libtayo (cemiplimab-rwlc) is payable for its FDA-approved indications. Libtayo (cemiplimab-rwlc) should be reported with not otherwise classified, or NOC, code J9999 and national drug code, or NDC, 61755-0008-01 until a permanent code is established.

Libtayo is approved for the treatment of patients with metastatic cutaneous squamous cell carcinoma, known as CSCC, or locally advanced CSCC who aren’t candidates for curative surgery or curative radiation. The recommended dosage of Libtayo is 350 mg as an intravenous infusion over 30 minutes every three weeks.

URMBT groups are excluded from coverage of this drug.

Medical drug management doesn’t require prior authorization for this drug.

Established
Q4131, Q4132, Q4133, Q4151**
Q4154**

Investigational
Q4100, Q4137, Q4138, Q4139, Q4140, Q4145, Q4148, Q4150, Q4153, Q4155, Q4156, Q4157, Q4159, Q4160, Q4162, Q4163, Q4168, Q4169, Q4170, Q4170, Q4171, Q4173, and Q4174

**New payable procedures

Basic benefit and medical policy

Amniotic membrane and amniotic fluid

The safety and effectiveness of select human amniotic membrane products have been established. They may be useful therapeutic options when indicated.

Injection of amniotic fluid is investigational for all indications. The safety, effectiveness and improvement in health outcomes haven’t been scientifically demonstrated.

This policy is effective March 1, 2019.

Inclusions:
Diabetic lower extremity ulcers

  • Treatment of nonhealing** diabetic lower-extremity ulcers using the following human amniotic membrane products (AmnioBand® Membrane, Biovance®, Epifix®, Grafix™)

**Nonhealing is defined as less than a 20% decrease in wound area with standard wound care for at least two weeks.

Ophthalmic conditions
Sutured human amniotic membrane grafts may be considered medically necessary for the treatment of any of the following indications:

  • Neurotrophic keratitis
  • Corneal ulcers and melts
  • Pterygium repair
  • Stevens-Johnson syndrome
  • Persistent epithelial defects when one of the following are met:
    • Failed to close completely after five days of conservative treatment
    • Failed to demonstrate a decrease in size after two days of conservative treatment

Conservative treatment is defined as the use of topical lubricants or topical antibiotics or therapeutic contact lens or patching.

Exclusions:

Ophthalmic conditions
Sutured human amniotic membrane grafts for the treatment of all other ophthalmic conditions, including, but not limited to:

  • Dry eye syndrome
  • Burns
  • Corneal perforation
  • Bullous keratopathy
  • Limbus stem cell deficiency and
  • After photorefractive keratectomy

Other conditions
All other human amniotic membrane products and indications not listed under inclusions, including, but not limited to:

  • Treatment of lower-extremity ulcers due to venous insufficiency
  • Human amniotic membrane without suture (e.g., Prokera®, AmbioDisk™) for ophthalmic indications
  • Injection of micronized or particulated human amniotic membrane for all indications, including but not limited to treatment of:
    • Osteoarthritis and plantar fasciitis
  • Injection of human amniotic fluid for all indications
UPDATES TO PAYABLE PROCEDURES

B4157, B4162

Basic benefit and medical policy

Medical formula for inborn errors of metabolism

The safety and effectiveness of oral medical formula for individuals with inborn errors of metabolism have been established. Oral medical formula is considered an established treatment option when policy criteria are met, effective Jan. 1, 2019.

Payment policy
Submit codes with BO modifier. Payable to durable medical equipment suppliers only. A maximum 30-day supply (per 25 days with a five-day grace period) is allowed.

Inclusions:
Oral medical formula (medical formula for consumption by mouth) for individuals of any age is considered established when all the following are met:

  • The individual has a diagnosis of an inborn error of metabolism.**
  • The oral medical formula is labeled and used for nutritional management of an IEM that interferes with the metabolism of specific nutrients (e.g., phenylketonuria, homocystinuria, maple syrup urine disease, etc.).
  • The oral medical formula nutrition is ordered by a clinical or medical biochemical geneticist.

** See appendix in medical policy for list of applicable diagnoses.

Exclusions:

  • Formula for any condition other than an inborn error of metabolism (e.g., diabetes, hypercholesterolemia, etc.)
  • Formula that doesn’t require a physician order for purchase
  • Formula not specifically used for the nutrition of an individual with IEM.
  • Medical food product that isn’t formula (e.g., food modified to be low in protein [meat or cheese substitutes, pasta, etc.])
  • Nutrition via tube feeding (refer to the Enteral Nutrition policy for guidelines)

J3590

Basic benefit and medical policy

JIVI (antihemophilic factor [recombinant] Pegylated-aucl)

JIVI® (antihemophilic factor [recombinant] Pegylated-aucl) is payable for its FDA-approved indications, effective Aug. 30, 2018.

JIVI, antihemophilic factor (recombinant), PEGylated-aucl, is a recombinant DNA-derived, Factor VIII concentrate indicated for use in previously treated adults and adolescents 12 years of age and older with hemophilia A (congenital Factor VIII deficiency) for on-demand treatment and control of bleeding episodes, perioperative management of bleeding and routine prophylaxis to reduce the frequency of bleeding episodes.

JIVI (antihemophilic factor [recombinant] Pegylated-aucl) should be reported with procedure code J7199 and NDC 00026-3942-25, 00026-3944-25, 00026-3946-25 or 00026-3948-25.

URMBT groups are excluded from coverage.

Pharmacy doesn’t require preauthorization for this drug.

J9171

Basic benefit and medical policy

Docefrez (docetaxel)

Docefrez (docetaxel) is established for the new FDA-approved indication for the treatment of castration-resistant prostate cancer, with prednisone in metastatic castration-resistant prostate cancer, effective Jan. 8, 2019.

POLICY CLARIFICATIONS

90649

Basic benefit and medical policy

Gardasil 9 (human papillomavirus 9-valent vaccine, recombinant)

Effective Oct. 5, 2018, Gardasil 9 (human papillomavirus 9-valent vaccine, recombinant) is covered through age 45 for the following FDA-approved indications:

Gardasil 9 (human papillomavirus 9-valent vaccine, recombinant) is a vaccine indicated in girls and women ages 9 through 45 for the prevention of the following diseases:

  • Cervical, vulvar, vaginal and anal cancer caused by human papillomavirus types 16, 18, 31, 33, 45, 52 and 58
  • Genital warts (condyloma acuminata) caused by HPV types 6 and 11

And the following precancerous or dysplastic lesions caused by HPV types 6, 11, 16, 18, 31, 33, 45, 52 and 58:

  • Cervical intraepithelial neoplasia, or CIN, grade 2/3 and cervical adenocarcinoma in situ, or AIS.
  • Cervical intraepithelial neoplasia grade 1
  • Vulvar intraepithelial neoplasia, or VIN, grade 2 and grade 3
  • Vaginal intraepithelial neoplasia, or VaIN, grade 2 and grade 3
  • Anal intraepithelial neoplasia, or AIN, grades 1, 2 and 3

Gardasil 9 (human papillomavirus 9-valent vaccine, recombinant) is indicated in boys and men ages 9 through 45 for the prevention of the following diseases:

  • Anal cancer caused by HPV types 16, 18, 31, 33, 45, 52 and 58
  • Genital warts (condyloma acuminata) caused by HPV types 6 and 11

And the following precancerous or dysplastic lesions caused by HPV types 6, 11, 16, 18, 31, 33, 45, 52 and 58:

  • Anal intraepithelial neoplasia grades 1, 2, and 3

Dosing information:
Ages 9 through 14 years:

  • Regimen: Two-dose schedule: 0, 6 to 12 months**
  • Regimen: Three-dose schedule: 0, 2, 6 months

Age 15 through 45 years:

  • Regimen: Three-dose schedule: 0, 2, 6 months

**If the second dose is administered earlier than five months after the first dose, administer a third dose at least four months after the second dose.

Pharmacy doesn’t require prior authorization of this drug.

NDCs: 00006-4119-01, 00006-4119-03, 00006-4121-01, 00006-4121-02

J0583

Basic benefit and medical policy

Angiomax (bivalirudin)

Effective Dec. 21, 2018, Angiomax (bivalirudin) is covered for the following updated FDA-approved indications:

Angiomax (bivalirudin) is indicated for use as an anticoagulant in patients undergoing percutaneous coronary intervention, known as PCI, including patients with heparin-induced thrombocytopenia, known as HIT, or heparin-induced thrombocytopenia and thrombosis syndrome, known as HITTS.

Dosing information:

  • The recommended dosage is a 0.75 mg/kg intravenous bolus dose followed immediately by a 1.75 mg/kg/h intravenous infusion for the duration of the procedure. Five minutes after the bolus dose has been administered, an activated clotting time should be performed and an additional bolus dose of 0.3 mg/kg should be given if needed.
  • Extending duration of infusion post-procedure up to four hours should be considered in patients with ST segment elevation MI, known as STEMI.

Pharmacy doesn’t require preauthorization of this drug.

NDC: 65293-0001-01

J9271

Basic benefit and medical policy

Keytruda (pembrolizumab)

Keytruda (pembrolizumab) is payable for the following new FDA indications:

  • Hepatocellular carcinoma, known as HCC: For the treatment of patients with HCC who have been previously treated with sorafenib.
  • Merkel cell carcinoma, known as MCC: For the treatment of adult and pediatric patients with recurrent locally advanced or metastatic Merkel cell carcinoma. This indication is approved under accelerated approval based on tumor response rate and durability of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in the confirmatory trials.
  • Urothelial carcinoma:
    • For the treatment of patients with locally advanced or metastatic urothelial carcinoma who aren’t eligible for cisplatin-containing chemotherapy and whose tumors express PD-L1 (Combined Positive Score [CPS] ≥10) as determined by an FDA-approved test, or in patients who aren’t eligible for any platinum-containing chemotherapy regardless of PD-L1 status
    • For the treatment of patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum containing chemotherapy

Dosage information:

  • Hepatocellular carcinoma: 200 mg every three weeks
  • Merkel cell carcinoma: 200 mg every three weeks for adults; 2 mg/kg (up to 200 mg) every three weeks for pediatrics
  • Urothelial carcinoma: 200 mg every three weeks

Pharmacy doesn’t require preauthorization of this drug.

NDCs: 00006-3026-01, 00006-3026-02

GROUP BENEFIT CHANGES

Lear Corporation

A company formerly called IMA has been acquired by Lear. Their group number is 71427. The group joins Blue Cross Blue Shield of Michigan, effective July 1, 2019.

Group number: 71427
Alpha prefix: PPO LRP and LPQ
Platform: NASCO hybrid

Plans offered: PPO, medical/surgical Dental Vision (VSP)

Note: The Federal Employee Program® follows its own criteria related to procedure codes J3490, J3590, J9271 and J9305.


Coding corner: Treating patients with seizure disorder

What is a seizure and how does it differ from epilepsy?

A seizure occurs from an episode of a sudden, uncontrolled electrical disturbance in the brain. It can cause abnormal movements and changes in awareness and behavior lasting anywhere from a few seconds to several minutes. Epilepsy is a condition characterized by recurrent seizures with no clear underlying cause. Status epilepticus describes a seizure that lasts longer than five minutes, or when seizures occur close together and the patient doesn't recover consciousness in between.

Depending on the type of seizure, signs and symptoms may include the following:

  • A staring spell
  • Uncontrollable jerking movements of the arms and legs
  • Loss of consciousness or awareness
  • Cognitive or emotional symptoms, such as fear, anxiety or déjà vu
  • Temporary confusion following a seizure (postictal state)

Seizures can be caused by many underlying conditions:

  • Congenital abnormalities
  • Head injuries
  • Poisoning
  • Stroke
  • Brain tumor

Documentation and coding tips

If known, provider documentation should specify the underlying cause of the seizure, such as:

  • Low blood sugar
  • Traumatic brain injury
  • Alcohol or drug use, abuse, dependence or withdrawal

To assign a code properly, documentation of the seizure type is required. The following are a few common types of seizures:

  • Tonic-clonic (grand mal)
  • Myoclonic
  • Atonic
  • Tonic
  • Clonic
  • Absence (petit mal)

For greater specificity, providers should also document the status of the seizure:

  • Intractable or not intractable
  • Presence or absence of status epilepticus

Provider documentation must also include the treatment plan, if known, or plans to refer the patient to a neurologist or other specialist for treatment:

  • Use of anti-convulsion medications such as carbamazepine, phenytoin, lamotrigine or levetiracetam
  • Surgery
  • Vagus nerve stimulation
  • Responsive neurostimulation
  • Deep brain stimulation

According to ICD-10-CM, a single seizure episode is classified to code R56.9, unspecified convulsions.

Epilepsy, or recurrent seizures, is classified to category G40. The ICD-10-CM coding system subcategorizes epilepsy even further:

  • Generalized versus localized epilepsy
  • Localized epilepsy with localized onset versus simple partial seizures

In addition, separate codes identify idiopathic versus symptomatic epilepsy with a fifth character to specify whether the seizures are intractable and a sixth character to identify the presence or absence of status epilepticus.

Some examples of seizure disorder codes appear in the chart below:

Condition ICD-10 code
Unspecified convulsions (seizures) R56.9
Post traumatic seizures R56.1
Epilepsy, unspecified, not intractable, without status epilepticus (seizure disorder) G40.909
Generalized idiopathic epilepsy and epileptic syndromes, not intractable with status epilepticus G40.301
Localization-related (focal or partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus G40.109
Absence epileptic syndrome, intractable, with status epilepticus G40.A11
Absence epileptic syndrome, not intractable, without status epilepticus G40.A09
Epileptic seizures related to external causes, not intractable, without status epilepticus G40.509

Sources:

  • www.mayoclinic.org**
  • 2019 ICD-10-CM Professional for Physicians

**Blue Cross Blue Shield of Michigan doesn’t own or control this website.

None of the information included in this article is intended to be legal advice and, as such, it remains the provider’s responsibility to ensure that all coding and documentation are done in accordance with all applicable state and federal laws and regulations.

Professional

We’re expanding medical coverage for U-M employees who are transgender

Blue Cross Blue Shield of Michigan and Blue Care Network will soon begin covering additional medical services for University of Michigan employees who are transgender.

The following additional gender-affirming services for members transitioning from male to female will be covered starting July 1, 2019:

  • Face and neck hair removal
  • Facial feminization surgery
  • Chondrolaryngoplasty (Adam’s apple reduction)

Currently, Blue Cross and BCN cover genital surgery, mastectomy in female-to-male transition, hormone therapy and counseling when medically necessary to treat gender dysphoria for U-M employees. Gender dysphoria involves a conflict between a person's gender identity and their gender assigned at birth, causing significant distress.

Coverage for the new services will require that members meet medical necessity criteria, use network providers and have up to a $30,000 lifetime limit. Michigan Medicine, formerly the University of Michigan Health System, is the only provider in our network that currently performs the facial feminization surgical services.

You can request authorizations for members who have a Blue Cross plan starting June 15, 2019. For members with a BCN plan, authorizations can be requested starting June 12.

The group number for Blue Cross members is 007005187, while the group number for BCN members is 00124316. The number will be on the front of their member ID card. As always, be sure to check web-DENIS for benefits and eligibility.

For more information
For more details, see the University of Michigan fact sheet on health plan coverage for gender-affirming services.

Transgender members may also use new coverage for fertility preservation if medical or surgical interventions related to their transition could result in infertility. For more details, see the University of Michigan fact sheet on coverage for services related to infertility.


You must use network laboratories for your Blue Cross and BCN patients

During our regular reviews of claims data, we’ve seen that a number of providers continue to send lab work for Blue Cross Blue Shield of Michigan and Blue Care Network patients to noncontracted laboratories. Also, we’ve found some patients are taking their scripts for lab work to noncontracted labs, not realizing this may result in higher costs.

When patients go out of network for lab services, it may cause unnecessary cost-sharing expenses and balance-billing by the labs — and we’re committed to helping control costs for our members. We encourage you let your patients know that going to a contracted lab helps ensure they avoid higher copayments and possible other out-of-pocket costs.

Network labs offer a full complement of routine tests, BRCA testing and other specialty testing. In addition, we use contracted labs to obtain lab data needed for regulatory reporting and clinical quality review.

According to your participation agreement, you must use network providers (including labs) when referring patients for non-emergency services. Make sure to verify a laboratory’s participation in the appropriate network before referring patients for lab samples.

Below is a list of labs used for our members:

Blue Cross PPO (commercial) Use the Find a Doctor tool on bcbsm.com (except MPSERS, Ford, GM)
Blue Cross PPO (commercial) for MPSERS, Ford, GM salaried employees Quest Diagnostics™ — 1-866-697-8378
Blue Cross Medicare Plus BlueSM PPO Quest Diagnostics — 1-866-697-8378
JVHL — 1-800-445-4979
BCN HMOSM (commercial) JVHL and JVHL subcontractors
1-800-445-4979
BCN AdvantageSM JVHL and JVHL subcontractors
1-800-445-4979

Failure to meet program requirements for using participating laboratory services may lead to corrective action, including potential termination from the Blue Cross network.


Medicare Part B medical specialty drug prior authorization list changing

Starting in June 2019, we’re adding the following medications to the Medicare Plus BlueSM PPO and BCN AdvantageSM Part B specialty prior-authorization drug list.

Medicare Plus Blue
For dates of service on or after June 3, 2019, the following medications will require prior authorization:

  • J3590 Ultomiris™
  • J9999 (C9044) Libtayo®
  • J3245 Ilumya™
  • Q5109 Ixifi™
  • J3590/J9999 Elzonris™
  • J3397 Mepsevii™
  • J3490 Tegsedi™
  • J9173 Imfinzi®
  • J3304 Zilretta®

We require prior authorization for these medications when you bill them electronically through an 837P transaction or on a professional CMS-1500 claim form for the following sites of care:

  • Physician office (place of service code 11)
  • Outpatient facility (place of service code 19, 22 or 24)

BCN Advantage
For dates of service on or after June 3, 2019, the following medications will require prior authorization:

  • J3590 Ultomiris™
  • J9999 (C9044) Libtayo®
  • J3245 Ilumya™
  • Q5109 Ixifi™
  • J3590/J9999 Elzonris™
  • J3397 Mepsevii™
  • J3490 Tegsedi™
  • J9173 Imfinzi®
  • J3304 Zilretta®

We require prior authorization for these medications when you bill them as a professional service or an outpatient facility service electronically through an 837P transaction or on a professional CMS-1500 claim form for:

  • Physician office (place of service code 11)
  • Outpatient facility (place of service code 19, 22 or 24)
  • Home (place of service code 12)

We also require prior authorization when you bill electronically through an 837I transaction or using a UB04 claim form for a hospital outpatient type of bill 013x.

Important reminder
You must get authorization before administering these medications. Use the NovoLogix® online tool to quickly submit your requests. It offers real-time status checks and immediate approvals for certain medications. Also note:

  • For BCN Advantage, if you have access to Provider Secured Services, you already have access to enter authorization requests through NovoLogix.
  • For Medicare Plus Blue, you can fax an Addendum P form to gain access to the NovoLogix online tool.

Cardiology procedures and in-lab sleep study assessments added to Medicare Plus Blue PPO radiology management program

On May 1, 2019, the radiology management program administered by AIM Specialty Health® added authorization requirements for select cardiology procedures and for in-lab sleep study assessments for Medicare Plus BlueSM PPO members.

The program includes UAW Retiree Medical Benefits Trust members with Medicare Plus Blue coverage.

Following are the CPT codes for the procedures that were added to the program.

Percutaneous coronary intervention:

  • *92920
  • *92924
  • *92928
  • *92933
  • *92937
  • *92943

Note: For these procedures, we require review for medical necessity and clinical appropriateness after the service has been completed. Due to the medical nature of this procedure, we don't require pre-service review for the codes listed above.

Diagnostic coronary catheterization:

  • *93454
  • *93455
  • *93456
  • *93457
  • *93458
  • *93459
  • *93460
  • *93461

Note: The diagnostic coronary catherization codes listed above require prior authorization.

In-lab sleep studies:

  • *95805
  • *95806
  • *95807
  • *95808
  • *95810
  • *95811

Note: The sleep study codes listed above require prior authorization.

Questions?

If you have questions, call 1-800-728-8008. You can also visit the AIM website.


Blue Cross makes changes to its drug testing policy on urine, oral fluids, hair

Approximately one-third of chronic pain patients don’t use opioids as prescribed or they abuse them, according to the American Society of Interventional Pain Physicians.

Sometimes this misuse can be categorized as substance use disorder. The medical community defines substance use disorder as the recurrent use of alcohol or drugs that causes clinically and functionally significant physical or mental impairment, disability, and failure to meet major responsibilities at work, school or home. Doctors diagnose substance use disorder when there is drug use combined with impaired control, social impairment and risky behavior.

One strategy for monitoring substance use disorder in patients is biologic specimen testing for the presence or absence of drugs. Currently, urine is the most commonly used biologic substance.

On May 1, 2019, Blue Cross Blue Shield of Michigan changed the reporting policy for definitive drug testing. A definitive drug test is one that’s medically necessary and clinically justified when the results of presumptive testing have been evaluated and support the need for follow-up definitive testing that will contribute to clinical decision making.

Procedure codes

  • Procedure codes G0480 through G0483 and G0659 should now be used for billing definitive drug testing.
  • Procedure codes *80320 through *80377 and *83992 are now considered informational and should continue to be billed in addition to the appropriate G-code for reporting purposes, effective Aug. 1, 2019.

Following are additional details related to the policy change:

Inclusions

  • Presumptive urine drug testing
    • For outpatient pain management, presumptive urine drug testing is used in:
      • Baseline screening at the initiation of treatment
      • Subsequent monitoring of treatment at an appropriate frequency, based on the risk level of the individual, including assessment of aberrant behavior
    • For outpatient substance use disorder treatment, presumptive urine drug testing used in:
      • Baseline screening at the initiation of treatment, one time per program entry
      • Weekly screening during the first four weeks of treatment
      • Subsequent targeted screening once every one to three months
    • For an individual not participating in outpatient pain management or outpatient substance use disorder treatment:
      • When a clinical evaluation suggests use of non-prescribed medications or illegal substances
  • Definitive and confirmatory urine drug testing
    • Definitive urine drug testing is used:
      • When immunoassays for the relevant drug or drugs aren’t commercially available
      • When definitive drug levels are required for clinical decision making

Exclusions:

  • Urine drug testing as a third-party requirement (for example, for employment, licensing or a court order)
  • Simultaneously testing for the same drug with both a blood and a urine specimen

Note: Oral fluid drug testing and hair drug testing are considered experimental.


Find out the next steps for CAQH Direct Assure 2.0

About 25% of our practitioners are currently participating in CAQH Direct Assure. We’ll continue rolling out Direct Assure in phases, with the goal of having all providers using Direct Assure by the end of December 2019.

The next step is to roll out Phase IV of Direct Assure at the end of June. Practitioners who will be included in this rollout are doctors who are likely to be audited by the Centers for Medicare & Medicaid Services:

  • Primary care physicians
  • Cardiologists
  • Oncologists
  • Ophthalmologists

What you need to do
To make a smooth transition to CAQH Direct Assure, continue to keep your CAQH record updated with your correct practice location information. You can familiarize yourself with the Direct Assure application by watching the Updating your practice locations in CAQH ProView video tutorial. This video will walk you through the screens and steps involved in providing your current location information to Blue Cross through CAQH.

While making updates to practice locations in CAQH, keep the following in mind:

  • If, after logging in to CAQH, you see a pop-up message that says Help Patients Find You, that means that you’re now participating in Direct Assure.
  • Once you’re active with Direct Assure, when you add, delete or update a group’s address in CAQH, that information will be sent to Blue Cross for processing.
  • Don’t forget to add your Type 2 NPI information for each location.
  • Selecting I see patients here one day per week or I see patients one day per month on the Practice Affiliation page will display the location in the directory. If a practitioner doesn’t offer appointments for patients at this location, he or she should select Other so the record doesn’t display in the directory.

If you have questions, you can reach out to CAQH directly at 1-888-599-1771 or contact Provider Enrollment at 1-800-822-2761.


We’re expanding CAQH ProView 3.0 to include delegated credentialing practitioners

Blue Cross Blue Shield of Michigan is expanding the use of the CAQH ProView 3.0 application. The application will include enrollment demographic and credentialing data for delegated credentialing practitioners.

The purpose of this initiative is to:

  • Streamline the data exchange process between delegated practitioner groups and Blue Cross.
  • Allow data to be exchanged consistently and more efficiently.
  • Improve our provider data quality for our members to view in our directories.

Blue Cross will be accepting automated data feeds from CAQH ProView 3.0 into our provider data repository, Portico. This automated process will make it more efficient for us to maintain provider data and will reduce duplication of data submission for the delegated groups.

We expect to begin beta testing this electronic data exchange with the University of Michigan Medical Group and Genesys PHO for initial enrollment and changes during the latter part of 2019, with the exchange of recredentialing data to follow.

Note: We still require signature documents for contracting. Continue to send these documents to the Provider Enrollment and Data Management department.


Discharge information may update automatically in e-referral for inpatient care

Recent updates to the e-referral system have improved the efficiency of inpatient authorizations for Michigan facilities. Blue Cross Blue Shield of Michigan and Blue Care Network obtain discharge information through Michigan Health Information Network Shared Services. Through upgrades to the process, e-referral may automatically populate changes to discharge dates.

  • If the discharge date results in a shorter length of stay than initially approved, e-referral will reduce the days on the approved case to match the facility’s date.
  • If the discharge date results in a longer length of stay than initially approved, e-referral will add the requested days and approve or pend the case.

This change applies to all Blue Cross and BCN fully approved cases in the e-referral system, including commercial and Medicare Advantage.

After adding an extension or reducing the number of days, the provider should confirm that the information in e-referral has been updated.

  • If the information is correct, no further action is needed.
  • If the information is incorrect, providers should contact the appropriate Blue Cross or BCN areas to relay the changes needed.

The updates are expected to reduce the need for providers to manually enter discharge information on a case.


Here’s helpful information about clinical editing appeals for Blue Cross PPO and Medicare Plus Blue claims

When we receive clinical editing appeals for PPO and Medicare Plus BlueSM PPO claims, we review the entire claim and all documentation provided. The goal of the review is to make sure that the documentation supports the services and procedures reported on the claim and that the claim follows correct coding and billing guidelines.

Occasionally, the documentation does not support the coding on the claim. When this happens, a recovery may occur on a code or service that wasn’t appealed. When this happens, you have a right to appeal the determination since it is a new edit or denial.

For more information, see your online provider manual.


Two Medicare star measures support statin therapy for patients with cardiovascular disease and diabetes

To underscore the importance of statin therapy, the Centers for Medicare & Medicaid Services includes two Medicare star measures aimed at its use for patients with cardiovascular disease and diabetes.

The Centers for Disease Control and Prevention estimates that adults with diabetes are 1.7 times more likely to die from cardiovascular disease than adults without it. Additionally, nearly two out of five people with diabetes who could benefit from statin therapy to lower their risk of heart attack, stroke and related deaths weren’t prescribed it, according to the Journal of the American College of Cardiology.

We encourage you to consider prescribing statins for your patients diagnosed with atherosclerotic cardiovascular disease and diabetes.

To learn more about the use of statin therapy, view these tip sheets:


Medication reconciliation reimbursement increases to $35 for Medicare Advantage members

When medication reconciliation is conducted within 30 days of a hospital discharge and a claim is submitted for CPT II code *1111F, Blue Cross Blue Shield of Michigan will reimburse providers $35 for its Medicare Advantage products: Medicare Plus BlueSM and BCN AdvantageSM. Blue Cross commercial continues to reimburse at $35.

Medication Reconciliation Post-Discharge is a HEDIS® measure.**

To receive reimbursement, follow these steps when patients are discharged after a hospital stay:

  • Schedule a medication reconciliation as soon as possible.
  • Perform medication reconciliation by comparing the hospital discharge medications against the patient’s current list of medications.
    • Physicians, physician assistants, pharmacists, registered nurses and nurse practitioners may conduct a medication reconciliation.
    • One example of acceptable documentation in the outpatient medical record is Current and discharge medications were reconciled.
  • Submit *1111F with the post-discharge office visit claim within 30 days of the discharge. The code description is Discharge medications reconciled with the current medication list in outpatient medical record.

About the HEDIS measure
Medication Reconciliation Post-Discharge assesses patients age 18 and older in the measurement year who were discharged from an acute or non-acute inpatient stay between Jan. 1 and Dec. 1 of the measurement year. It looks at patients whose medications were reconciled from the date of discharge through 30 days after discharge (31 days total).

Click here to review the Medication Reconciliation Post-Discharge tip sheet.

**HEDIS® is a registered trademark of the National Committee for Quality Assurance.


Managing acute low back pain in adults

Many adults will experience low back pain at some point in their life. More than 25% of adults say they’ve experienced back pain in the past three months, according to the National Institute of Neurological Disorders and Stroke. Most of the time, low back pain is easily treated or will resolve on its own.

Imaging for acute low back pain usually isn’t required within the first six weeks, unless certain red flags are present. These include:

  • Infection
  • Spinal fracture
  • Leg weakness
  • Loss of bladder control or bowel control
  • Numbness or tingling
  • Fever

A conservative approach is generally considered preferable if red flags aren’t present.

In 2018, the Michigan Quality Improvement Consortium published a guideline** for adults with low back pain or back-related leg symptoms for more than six weeks. The following are some of the focus areas recommended by the consortium when treating patients with low back pain:

  • Performing a history and physical exam
  • Encouraging patients to stay active within the limits permitted by pain
  • Referring to non-invasive therapy if the patient experiences persistent disability at two weeks
  • Prescribing medication on a time-contingent basis, not a pain-contingent basis.
  • Offering reassurance

**Blue Cross Blue Shield of Michigan doesn’t own or control this website.

Facility

We’re expanding medical coverage for U-M employees who are transgender

Blue Cross Blue Shield of Michigan and Blue Care Network will soon begin covering additional medical services for University of Michigan employees who are transgender.

The following additional gender-affirming services for members transitioning from male to female will be covered starting July 1, 2019:

  • Face and neck hair removal
  • Facial feminization surgery
  • Chondrolaryngoplasty (Adam’s apple reduction)

Currently, Blue Cross and BCN cover genital surgery, mastectomy in female-to-male transition, hormone therapy and counseling when medically necessary to treat gender dysphoria for U-M employees. Gender dysphoria involves a conflict between a person's gender identity and their gender assigned at birth, causing significant distress.

Coverage for the new services will require that members meet medical necessity criteria, use network providers and have up to a $30,000 lifetime limit. Michigan Medicine, formerly the University of Michigan Health System, is the only provider in our network that currently performs the facial feminization surgical services.

You can request authorizations for members who have a Blue Cross plan starting June 15, 2019. For members with a BCN plan, authorizations can be requested starting June 12.

The group number for Blue Cross members is 007005187, while the group number for BCN members is 00124316. The number will be on the front of their member ID card. As always, be sure to check web-DENIS for benefits and eligibility.

For more information
For more details, see the University of Michigan fact sheet on health plan coverage for gender-affirming services.

Transgender members may also use new coverage for fertility preservation if medical or surgical interventions related to their transition could result in infertility. For more details, see the University of Michigan fact sheet on coverage for services related to infertility.


You must use network laboratories for your Blue Cross and BCN patients

During our regular reviews of claims data, we’ve seen that a number of providers continue to send lab work for Blue Cross Blue Shield of Michigan and Blue Care Network patients to noncontracted laboratories. Also, we’ve found some patients are taking their scripts for lab work to noncontracted labs, not realizing this may result in higher costs.

When patients go out of network for lab services, it may cause unnecessary cost-sharing expenses and balance-billing by the labs — and we’re committed to helping control costs for our members. We encourage you let your patients know that going to a contracted lab helps ensure they avoid higher copayments and possible other out-of-pocket costs.

Network labs offer a full complement of routine tests, BRCA testing and other specialty testing. In addition, we use contracted labs to obtain lab data needed for regulatory reporting and clinical quality review.

According to your participation agreement, you must use network providers (including labs) when referring patients for non-emergency services. Make sure to verify a laboratory’s participation in the appropriate network before referring patients for lab samples.

Below is a list of labs used for our members:

Blue Cross PPO (commercial) Use the Find a Doctor tool on bcbsm.com (except MPSERS, Ford, GM)
Blue Cross PPO (commercial) for MPSERS, Ford, GM salaried employees Quest Diagnostics™ — 1-866-697-8378
Blue Cross Medicare Plus BlueSM PPO Quest Diagnostics — 1-866-697-8378
JVHL — 1-800-445-4979
BCN HMOSM (commercial) JVHL and JVHL subcontractors
1-800-445-4979
BCN AdvantageSM JVHL and JVHL subcontractors
1-800-445-4979

Failure to meet program requirements for using participating laboratory services may lead to corrective action, including potential termination from the Blue Cross network.


Update: naviHealth managing authorizations for MA members moving to post-acute care facilities

A few training sessions remain for health care providers to learn more about naviHealth’s clinical model and provider portal.

As you read in a May Record article, naviHealth will be managing authorizations for Medicare Plus BlueSM PPO and BCN AdvantageSM members who are moving into skilled nursing, long-term acute care and inpatient rehabilitation facilities. The transition to naviHealth is effective for authorization requests submitted for admission dates on or after June 1, 2019, for both in-state and out-of-state cases.

Following is the schedule for remaining webinar dates and times. Click here to register.

Acute care hospitals Wednesday, June 5, 8 to 9:30 a.m.
Skilled nursing facilities Wednesday, June 5, 11:30 a.m. to 1:30 p.m.
Inpatient rehabilitation facilities and long-term acute care hospitals Thursday, June 6, 11:30 a.m. to 1 p.m.

Here’s some additional information to keep in mind:

  • Post-acute care facilities should always check to see if an authorization is in place when they’re handling an admission for a Medicare Advantage patient. If an authorization wasn’t submitted by the acute care facility, then the post-acute care facility should submit the authorization request.
  • Retrospective authorizations can be submitted electronically up to 90 days post-discharge from an acute care facility. Beyond 90 days, authorizations must be phoned in or faxed.

For more details on how to submit authorization requests, see the May Record article.

To access an FAQ on post-acute care services, click here.


Here’s what you need to know about prior authorization requirements for acute detoxification

Members with Blue Cross Blue Shield of Michigan commercial PPO health plans require prior authorizations for uncomplicated acute detoxification through New Directions. To submit a prior authorization request to New Directions, call 1-800-762-2382 or visit New Directions WebPass.

This prior authorization requirement is for members with Blue Cross health plans that include behavioral health benefits. Groups with behavioral health benefits carved out are excluded.

Keep the following in mind:

  • When members need detoxification, but a medical condition, such as acute pancreatitis, chest pains or dehydration, is the primary focus of care, authorization should be obtained from Blue Cross through the e-referral system.
  • If a member has been admitted for acute detoxification and then develops acute medical complications, you must request authorization through e-referral — even if you’ve already received prior authorization for acute detoxification through New Directions.

Medicare Part B medical specialty drug prior authorization list changing

Starting in June 2019, we’re adding the following medications to the Medicare Plus BlueSM PPO and BCN AdvantageSM Part B specialty prior-authorization drug list.

Medicare Plus Blue
For dates of service on or after June 3, 2019, the following medications will require prior authorization:

  • J3590 Ultomiris™
  • J9999 (C9044) Libtayo®
  • J3245 Ilumya™
  • Q5109 Ixifi™
  • J3590/J9999 Elzonris™
  • J3397 Mepsevii™
  • J3490 Tegsedi™
  • J9173 Imfinzi®
  • J3304 Zilretta®

We require prior authorization for these medications when you bill them electronically through an 837P transaction or on a professional CMS-1500 claim form for the following sites of care:

  • Physician office (place of service code 11)
  • Outpatient facility (place of service code 19, 22 or 24)

BCN Advantage
For dates of service on or after June 3, 2019, the following medications will require prior authorization:

  • J3590 Ultomiris™
  • J9999 (C9044) Libtayo®
  • J3245 Ilumya™
  • Q5109 Ixifi™
  • J3590/J9999 Elzonris™
  • J3397 Mepsevii™
  • J3490 Tegsedi™
  • J9173 Imfinzi®
  • J3304 Zilretta®

We require prior authorization for these medications when you bill them as a professional service or an outpatient facility service electronically through an 837P transaction or on a professional CMS-1500 claim form for:

  • Physician office (place of service code 11)
  • Outpatient facility (place of service code 19, 22 or 24)
  • Home (place of service code 12)

We also require prior authorization when you bill electronically through an 837I transaction or using a UB04 claim form for a hospital outpatient type of bill 013x.

Important reminder
You must get authorization before administering these medications. Use the NovoLogix® online tool to quickly submit your requests. It offers real-time status checks and immediate approvals for certain medications. Also note:

  • For BCN Advantage, if you have access to Provider Secured Services, you already have access to enter authorization requests through NovoLogix.
  • For Medicare Plus Blue, you can fax an Addendum P form to gain access to the NovoLogix online tool.

Cardiology procedures and in-lab sleep study assessments added to Medicare Plus Blue PPO radiology management program

On May 1, 2019, the radiology management program administered by AIM Specialty Health® added authorization requirements for select cardiology procedures and for in-lab sleep study assessments for Medicare Plus BlueSM PPO members.

The program includes UAW Retiree Medical Benefits Trust members with Medicare Plus Blue coverage.

Following are the CPT codes for the procedures that were added to the program.

Percutaneous coronary intervention:

  • *92920
  • *92924
  • *92928
  • *92933
  • *92937
  • *92943

Note: For these procedures, we require review for medical necessity and clinical appropriateness after the service has been completed. Due to the medical nature of this procedure, we don't require pre-service review for the codes listed above.

Diagnostic coronary catheterization:

  • *93454
  • *93455
  • *93456
  • *93457
  • *93458
  • *93459
  • *93460
  • *93461

Note: The diagnostic coronary catherization codes listed above require prior authorization.

In-lab sleep studies:

  • *95805
  • *95806
  • *95807
  • *95808
  • *95810
  • *95811

Note: The sleep study codes listed above require prior authorization.

Questions?

If you have questions, call 1-800-728-8008. You can also visit the AIM website.


Discharge information may update automatically in e-referral for inpatient care

Recent updates to the e-referral system have improved the efficiency of inpatient authorizations for Michigan facilities. Blue Cross Blue Shield of Michigan and Blue Care Network obtain discharge information through Michigan Health Information Network Shared Services. Through upgrades to the process, e-referral may automatically populate changes to discharge dates.

  • If the discharge date results in a shorter length of stay than initially approved, e-referral will reduce the days on the approved case to match the facility’s date.
  • If the discharge date results in a longer length of stay than initially approved, e-referral will add the requested days and approve or pend the case.

This change applies to all Blue Cross and BCN fully approved cases in the e-referral system, including commercial and Medicare Advantage.

After adding an extension or reducing the number of days, the provider should confirm that the information in e-referral has been updated.

  • If the information is correct, no further action is needed.
  • If the information is incorrect, providers should contact the appropriate Blue Cross or BCN areas to relay the changes needed.

The updates are expected to reduce the need for providers to manually enter discharge information on a case.


Here’s helpful information about clinical editing appeals for Blue Cross PPO and Medicare Plus Blue claims

When we receive clinical editing appeals for PPO and Medicare Plus BlueSM PPO claims, we review the entire claim and all documentation provided. The goal of the review is to make sure that the documentation supports the services and procedures reported on the claim and that the claim follows correct coding and billing guidelines.

Occasionally, the documentation does not support the coding on the claim. When this happens, a recovery may occur on a code or service that wasn’t appealed. When this happens, you have a right to appeal the determination since it is a new edit or denial.

For more information, see your online provider manual.

Pharmacy

Medicare Part B medical specialty drug prior authorization list changing

Starting in June 2019, we’re adding the following medications to the Medicare Plus BlueSM PPO and BCN AdvantageSM Part B specialty prior-authorization drug list.

Medicare Plus Blue
For dates of service on or after June 3, 2019, the following medications will require prior authorization:

  • J3590 Ultomiris™
  • J9999 (C9044) Libtayo®
  • J3245 Ilumya™
  • Q5109 Ixifi™
  • J3590/J9999 Elzonris™
  • J3397 Mepsevii™
  • J3490 Tegsedi™
  • J9173 Imfinzi®
  • J3304 Zilretta®

We require prior authorization for these medications when you bill them electronically through an 837P transaction or on a professional CMS-1500 claim form for the following sites of care:

  • Physician office (place of service code 11)
  • Outpatient facility (place of service code 19, 22 or 24)

BCN Advantage
For dates of service on or after June 3, 2019, the following medications will require prior authorization:

  • J3590 Ultomiris™
  • J9999 (C9044) Libtayo®
  • J3245 Ilumya™
  • Q5109 Ixifi™
  • J3590/J9999 Elzonris™
  • J3397 Mepsevii™
  • J3490 Tegsedi™
  • J9173 Imfinzi®
  • J3304 Zilretta®

We require prior authorization for these medications when you bill them as a professional service or an outpatient facility service electronically through an 837P transaction or on a professional CMS-1500 claim form for:

  • Physician office (place of service code 11)
  • Outpatient facility (place of service code 19, 22 or 24)
  • Home (place of service code 12)

We also require prior authorization when you bill electronically through an 837I transaction or using a UB04 claim form for a hospital outpatient type of bill 013x.

Important reminder
You must get authorization before administering these medications. Use the NovoLogix® online tool to quickly submit your requests. It offers real-time status checks and immediate approvals for certain medications. Also note:

  • For BCN Advantage, if you have access to Provider Secured Services, you already have access to enter authorization requests through NovoLogix.
  • For Medicare Plus Blue, you can fax an Addendum P form to gain access to the NovoLogix online tool.

Stimulant drugs will have new quantity limits starting July 1, 2019

On July 1, 2019, Blue Cross Blue Shield of Michigan will implement new quantity limits for stimulant drugs, as shown in the table below. This change only affects our commercial (non-Medicare) members who have Blue Cross pharmacy benefits.

Our goal is to provide our members with safe, high-quality prescription drugs. In May, we sent letters to notify members who may be affected by these quantity limit changes. The letters encourage members to discuss treatment options with their physicians.

If necessary, you can request an override of the quantity limits for your patients. The request should include documentation stating that the amount you’re prescribing is medically necessary.

To get a form for a quantity limit override, log in as a provider at bcbsm.com/providers or call the Pharmacy Services Clinical Help Desk at 1-800-437-3803 and select Option 1.

Here are quantity limits for stimulant drugs, effective July 1, 2019:

Drug name
(generic name)
Strength Quantity covered
Concerta
(methylphenidate tablet extended release)
18mg, 27mg, 36mg, 54mg 2 tablets/day
Daytrana
(methylphenidate transdermal patch)
10mg/9hr, 15mg/9hr, 20mg/9hr, 30mg/9hr 1 patch/day
Desoxyn
(methamphetamine tablet)
5mg 5 tablets/day
Dexedrine
(dextroamphetamine sulfate capsule extended, dextroamphetamine tablets)
5mg, 10mg, 15mg 4 tablets or capsules/day
Focalin
(dexmethylphenidate tablet)
2.5mg, 5mg, 10mg 3 tablets/day
Focalin XR
(dexmethylphenidate capsule extended release)
5mg, 10mg, 15mg, 20mg, 25mg, 30mg, 35mg, 40mg 2 capsules/day
Metadate CD ≤ 30 mg
(methylphenidate capsule extended release)
10mg, 20mg, 30mg 3 capsules/day
Metadate CD > 30 mg
(methylphenidate capsule extended release)
40mg, 50mg, 60mg 2 capsules/day
Methylin
(methylphenidate chewable tablet)
2.5mg, 5mg, 10mg, 20mg 7 tablets/day
Methylin Er / Metadate ER
(methylphenidate tablet extended release)
10mg, 20mg 6 tablets/day
Methylin Solution
(methylphenidate solution)
5mg/5ml, 10mg/5ml 80mg/day
Procentra
(dextroamphetamine solution)
5mg/5ml 60mg/day
Ritalin
(methylphenidate tablet)
5mg, 10mg, 20mg 7 tablets/day
Ritalin LA ≤ 30 mg
(methylphenidate capsule extended release)
10mg, 20mg, 30mg 4 capsules/day
Ritalin LA 40 mg
(methylphenidate capsule extended release)
40mg 3 capsules/day
Ritalin LA 60 mg
(methylphenidate capsule extended release)
60mg 2 capsules/day
Ritalin SR
(methylphenidate tablet sustained release)
20mg 6 tablets/day
Strattera
(atomoxetine capsule)
10mg, 18mg, 25mg, 40mg, 60mg, 80mg, 100mg 2 capsules/day
Zenzedi
(dextroamphetamine tablet)
2.5mg, 5mg, 7.5mg, 10mg, 15mg, 20mg, 30mg 4 tablets/day

No portion of this publication may be copied without the express written permission of Blue Cross Blue Shield of Michigan, except that BCBSM participating health care providers may make copies for their personal use. In no event may any portion of this publication be copied or reprinted and used for commercial purposes by any party other than BCBSM.

*CPT codes, descriptions and two-digit numeric modifiers only are copyright 2018 American Medical Association. All rights reserved.