Neurotron Inc. v. Medical Service Association of Pennsylvania, Inc., T/a Pennsylvania Blue Shield Highmark, Inc

254 F.3d 444, 2001 U.S. App. LEXIS 13757, 2001 WL 689523
CourtCourt of Appeals for the Third Circuit
DecidedJune 19, 2001
Docket00-1516
StatusPublished
Cited by19 cases

This text of 254 F.3d 444 (Neurotron Inc. v. Medical Service Association of Pennsylvania, Inc., T/a Pennsylvania Blue Shield Highmark, Inc) 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
Neurotron Inc. v. Medical Service Association of Pennsylvania, Inc., T/a Pennsylvania Blue Shield Highmark, Inc, 254 F.3d 444, 2001 U.S. App. LEXIS 13757, 2001 WL 689523 (3d Cir. 2001).

Opinion

OPINION OF THE COURT

STAPLETON, Circuit Judge:

Neurotron, Inc. (“Neurotron”) is a Maryland corporation which manufactures an electrodiagnostic medical testing device known as the Neurometer CPT (“Neurom-eter”). Highmark, Inc. (“Highmark”) 1 is a Pennsylvania corporation engaged in the operation of nonprofit health care plans. Neurotron alleges that a passage in High-mark’s newsletter, Policy Review and News (“PRN”), commercially disparaged the Neurometer. Highmark successfully moved for summary judgment. Neurotron appeals. We will affirm.

I.

The Neurometer tests a patient’s ability to perceive small electrical currents through a procedure known as “current perception threshold” testing (“CPT”). CPT involves connecting electrodes to the surface of the patient’s skin and then delivering a series of low-voltage electrical shocks and recording whether the shocks were perceived. Through a series of shocks at decreasing voltages, the Neu-rometer establishes the lowest level of current that the patient is able to feel. It then compares these readings to a database of “normal” readings and delivers a printout that states whether the patient’s sensory perception of electrical current is either elevated (“hyperesthesia”), normal, or depressed (“hypoesthesia”). Hyper-esthesia and hypoesthesia can be symptoms of numerous medical problems. Neurotron contends that the Neurometer is a useful diagnostic tool because it can *446 detect these symptoms at a very early stage.

Highmark provides nonprofit health insurance programs which cover the medical expenses of Highmark members. Among the services that Highmark excludes from payment are services that are experimental or investigational. Its agreement with its members and health care providers stipulates that Highmark “does not cover services which it determines are Experimental or Investigative in nature because those services are not accepted by the broad medical community as effective treatments.” App. III at 298a. That agreement defines “Experimental or Investigative” as follows:

the use of any ... procedure ... which[Highmark], relying on the advice of the general medical community which includes but is not limited to medical consultants, medical journals and/or governmental regulations, does not accept as standard medical treatment of the condition being treated, or any such items requiring federal or other governmental agency approval for which approval has not been granted at the time the services were rendered.

App. Ill at 300a.

Highmark’s Medical Policy Department (“MPD”) reviews developments in health care practice and procedure and makes determinations as to when a new product or procedure has advanced beyond the experimental or investigational stage and becomes an accepted part of standard medical practice. Highmark’s Benefits Utilization Management Department (“BUMD”) conducts post-payment audits of health care providers to assure that their billings to Highmark have been in accordance with the applicable policies and regulations, that services are reported and paid accurately, and that unnecessary services are not being prescribed.

In October of 1990, Ralph Cohen, Neu-rotron’s President, wrote to Highmark requesting that the Neurometer be reviewed and evaluated for coverage. Highmark referred the request to the MPD which, pursuant to Highmark’s policy, initiated a “consultant review.” Three independent neurologists, Drs. Brennan, Jeffries, and Lossing, evaluated the Neurometer and CPT. Based upon the consultant review, Highmark concluded that CPT was investi-gational in nature and was, therefore, an uncovered service.

In October of 1991, Dr. Jefferson Ka-tims, Neurotron’s Director of Research, wrote to Highmark to request again that the Neurometer be reviewed and evaluated for coverage. Dr. Joseph Ricci, High-mark’s Vice President for Medical Affairs, responded in November of 1991 that High-mark’s opinion remained unchanged and that, consequently, CPT would remain noncovered.

In 1994, Dr. Katims again wrote to Dr. Ricci to request reevaluation of CPT. Dr. Ricci referred the request to the MPD for review by Douglas Worley. Worley solicited advice from Drs. Lossing, Samuels, and Silverman. Based upon the advice of these independent consultants, Highmark concluded that CPT continued to be inves-tigational. Highmark added CPT to Medical Policy Bulletin Z-24 which listed numerous products and procedures which were not covered because they had been determined to be investigational.

In 1996, Emelie Sconing, Manager of the BUMD, conducted a claims review of certain chiropractors who appeared to be inappropriately billing noncovered CPT as covered nerve conduction velocity tests. She sent the claims files of the providers under investigation to consultants for review. The consultants, Drs. Tarola and Samuels, concluded that the providers un *447 der investigation had actually performed CPT and not nerve conduction velocity tests. Dr. Tarola opined that “CPT is a nonspecific electrodiagnostic procedure that lacks proof of validity and reliability, and has limited clinical utility.” App. Ill at 223a. He concluded that “the CPT’s performed on the above referenced patients were medically unnecessary because of apparent indiscriminate use of the procedure and its lack of validity, reliability, and clinical utility.” Id. at 224a. Dr. Samuels opined that a “CPT test is experimental and of no proven clinical value. It is not a nerve conduction test. All of these claims should be denied.” Id. at 225a.

Having concluded that health care providers were submitting claims for covered nerve conduction velocity tests when in fact they were performing noncovered CPT, Sconing asked the MPD to prepare a notice for publication in Highmark’s newsletter, PRN, that CPT tests were not permissibly billed as nerve conduction velocity tests. Highmark uses the PRN to communicate medical policies and other information to its participating health care providers.

Worley drafted the requested notice by adopting the language of Dr. Samuels’ comments assessing CPT testing. The notice appeared in the February, 1997, edition of the PRN and read, in its entirety, as follows:

Neuro-selective current perception threshold test
The neuro-selective current perception threshold test is performed to provide an objective measure of subjective sensation. It requires the patient’s conscious perception of the stimulation applied. The neuro-selective current perception threshold test has no proven clinical utility and is not eligible for payment, since it is considered to be investigational.
Use procedure code 95999 to report this service.

The District Court found that although the passage did not refer specifically to Neuro-tron or the Neurometer, there was sufficient evidence for a reasonable factfinder to find that the passage could be understood as referring to the Neurometer. The District Court also found that there was a genuine issue of material fact as to whether the PRN article was false.

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254 F.3d 444, 2001 U.S. App. LEXIS 13757, 2001 WL 689523, Counsel Stack Legal Research, https://law.counselstack.com/opinion/neurotron-inc-v-medical-service-association-of-pennsylvania-inc-ta-ca3-2001.