Cardionet, Inc. v. Cigna Health Corp.

751 F.3d 165, 58 Employee Benefits Cas. (BNA) 1001, 2014 WL 1778149, 2014 U.S. App. LEXIS 8468
CourtCourt of Appeals for the Third Circuit
DecidedMay 6, 2014
Docket13-2496
StatusPublished
Cited by156 cases

This text of 751 F.3d 165 (Cardionet, Inc. v. Cigna Health Corp.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Third Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Cardionet, Inc. v. Cigna Health Corp., 751 F.3d 165, 58 Employee Benefits Cas. (BNA) 1001, 2014 WL 1778149, 2014 U.S. App. LEXIS 8468 (3d Cir. 2014).

Opinion

OPINION OF THE COURT

FUENTES, Circuit Judge:

CardioNet, Inc. and LifeWatch Services, Inc. are providers of medical devices that allow physicians to monitor cardiac arrhythmias in patients not confined to the hospital. For several years, CIGNA Health Corporation provided coverage for this service. Then, in 2012, CIGNA reversed course and announced that it would no longer do so. CardioNet and Life-Watch filed this action against CIGNA on their own behalf and as the assignee of patients who used their services. In response, CIGNA moved to compel arbitration under the parties’ agreement. The District Court agreed with CIGNA that CardioNet and LifeWatch’s claims fell within the arbitration clause of the parties’ agreement and therefore compelled arbitration. Because we conclude that none of CardioNet and LifeWatch’s claims fall within the arbitration clause, we vacate the District Court’s judgment and remand for further proceedings.

I. 2

A.

CardioNet, Inc. and LifeWatch Services, Inc. (together, “the Providers”) supply outpatient cardiac telemetry (“OCT”) services. OCT, an outpatient device, is used by physicians, usually cardiologists, to monitor cardiac arrhythmias. The device differs from conventional technologies for detecting arrhythmias in that it transmits electrocardiographic (“EKG”) data in real time to certified technicians, who then forward the data to the ordering physician. OCT is approved by the Food and Drug Administration, and has been covered by Medicare and commercial insurers for many years.

CIGNA Healthcare Corporation administers employer sponsored health and welfare benefit plans across the country. Like other health insurance companies, CIGNA maintains a network of health care providers. Pursuant to individual agreements between CIGNA and its in-network providers, CIGNA pays the providers directly for the services rendered to patients.

In 2007, CardioNet and LifeWatch joined CIGNA’s provider network by en *169 tering into identical Administrative Service Agreements with CIGNA (“the Agreement”). The Agreement sets the rate at which CIGNA would reimburse the Providers for the particular services rendered to CIGNA patients. It also circumscribes the services for which reimbursement is available. Specifically, the Providers’ services are reimbursable under the Agreement only if they constitute “Covered Services.” App. at 65, 72. The Agreement defines “Covered Services” as “those health care services for which a Participant is entitled to receive coverage under the terms and conditions of the Participant’s Benefit Plan.” Id. at 64. 3 According to the Agreement, “[n]o service is a Covered Service unless it is Medically Necessary,” that is it “satisfies the Medical Necessity requirements under the applicable Benefit Plan.” Id.

B.

CIGNA first announced a policy of covering OCT in 2007. At the time, it determined that there was “sufficient evidence in the published peer reviewed medical literature supporting the use of home-based, real-time surveillance systems.” App. at 35. CIGNA maintained and reaffirmed its policy of covering OCT each year through 2011. But then, in 2012, it abruptly terminated its coverage of OCT; CIGNA then issued a new policy statement, entitled 2012 Cardiac Event Monitor Coverage Policy (“the 2012 Policy”), announcing that it would no longer cover OCT “for any indication because it is considered experimental, investigational or unproven.” Id. at 25, 37. The 2012 Policy acknowledged, however, that this new position would be trumped by any conflicting language in the coverage policies themselves.

Although CIGNA’s OCT policy had changed, its medical knowledge had not: CIGNA relied on the same medical literature it had previously relied upon in concluding that OCT should be covered. Shortly after CIGNA’s announcement, the Providers asked CIGNA to reconsider its new position on OCT. According to the Complaint, CIGNA intimated to the Providers that its motive for reversing course was financial, but refused to back away from the 2012 Policy.

Subsequently, CIGNA issued Medical Coverage Policy Updates for Health Care Professionals (“the Physician Update”) to hundreds of thousands of its network physicians, announcing that it would not cover OCT “for any indication because it is considered [experimental, investigational, and unproven].” App. 40-41. By letter, CardioNet objected to CIGNA’s characterization of OCT as experimental, investigational, and unproven. CardioNet’s letter also observed that CIGNA’s unequivocal statement that CIGNA would not cover OCT “for any indications” conflicted with its acknowledgement in the 2012 Policy that CIGNA’s new position could be trumped by the specific coverage policies included in employee benefit plans. Id. CIGNA neither responded to the letter nor amended the Physician Update. The Providers allege that the Physician Update not only prevented patients with CIGNA insurance from ordering OCT, but also “has caused and continues to cause physicians to refrain from ordering OCT for patients whose employer plans ... do cover OCT.” Id. at 41.

C.

The Providers filed this action in the Eastern District of Pennsylvania, “on their *170 own behalves and as assignees of the rights and claims of patients.” App. at 24. The Complaint contains seven counts. The Providers bring Counts I-IV as the assignees of the claims of five CIGNA plan participants (“the Participants”). The Participants all sought coverage for OCT after the implementation of the 2012 Policy, and were all denied coverage by CIG-NA. After CIGNA denied coverage, the Participants received OCT from the Providers, and in exchange assigned to the Providers “all of [their] rights (without limitation) under the Employee Retirement Income Security Act of 1974 (ERISA) ... along with any other rights under federal or state law that [they] may have as related to the reimbursement of coverage” for the. uncovered treatment. Id. at 284.

Counts I-IV, the so-called “derivative” counts, challenge CIGNA’s decision to deny the Participants OCT coverage; the Providers bring these claims standing in the shoes of the Participants. Specifically, in Count I, the Providers allege that CIG-NA arbitrarily and capriciously changed its OCT coverage policy, and seek to recover benefits due under ERISA § 502(a)(1)(B), 29 U.S.C. § 1132(a)(1)(B). In Count II, the Providers seek an injunction, pursuant to ERISA § 502(a)(3), 29 U.S.C. § 1132(a)(3), directing CIGNA to withdraw its current coverage policy for OCT and rescind the Physician Update regarding OCT. In Count III, the Providers allege that, by systematically denying OCT coverage, CIGNA breached its duty to the Participants to faithfully apply the terms of the governing ERISA plans; they seek an injunction, pursuant to ERISA § 502(a)(3), “requiring CIGNA to process claims for OCT benefits in all instances based on the terms of the ERISA plans ...

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751 F.3d 165, 58 Employee Benefits Cas. (BNA) 1001, 2014 WL 1778149, 2014 U.S. App. LEXIS 8468, Counsel Stack Legal Research, https://law.counselstack.com/opinion/cardionet-inc-v-cigna-health-corp-ca3-2014.