United States of America v. AthenaHealth, Inc

CourtDistrict Court, D. Massachusetts
DecidedMarch 3, 2022
Docket1:17-cv-12125
StatusUnknown

This text of United States of America v. AthenaHealth, Inc (United States of America v. AthenaHealth, Inc) is published on Counsel Stack Legal Research, covering District Court, D. Massachusetts primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States of America v. AthenaHealth, Inc, (D. Mass. 2022).

Opinion

United States District Court District of Massachusetts

) United States of America, ) ) Plaintiff, ) ) v. ) ) Civil Action No. AthenaHealth, Inc., et al., ) 17-12125-NMG ) Defendants. ) )

MEMORANDUM & ORDER GORTON, J. This dispute over attorneys’ fees and costs arises from the settlement of two qui tam actions brought against defendant AthenaHealth, Inc. (“Athena” or “defendant”) pursuant to the False Claims Act (“the FCA”), 37 U.S.C. § 3729 et seq. The first action was filed by relator Geordie Sanborn in October, 2017, alleging violations of the FCA and the federal anti- kickback statute (“the AKS”), 42 U.S.C. § 1320a-7b. Two months later, relators William McKusick and Cheryl Lovell filed a second qui tam action against Athena, alleging violations of the same statutes. In January, 2021, the government intervened in some, but not all, of the relators’ claims and shortly thereafter entered into an agreement with Athena to settle the action (“the Settlement Agreement”) for approximately $18.25 million, a portion of which was set aside for Sanborn as a relator’s share. See 31 U.S.C. § 3730(d). Sanborn, McKusick and Lovell separately agreed to divide that share among themselves.

The Settlement Agreement reserved to relators the right to seek reasonable expenses, costs and attorneys’ fees from Athena to the extent provided for by the FCA. See 31 U.S.C. § 3730(d). After unsuccessful negotiations, relators filed the pending motions for such funds which Athena opposes. For the reasons that follow, the motion of relators McKusick and Lovell (Docket No. 82) will be denied. The motion of relator Sanborn (Docket No. 77) will be allowed, in part, and denied, in part. I. Background A. The False Claims Act and the Anti-Kickback Statute The FCA is among the government’s “primary litigative tool[s] for combatting fraud” concerning public funds. United

States v. Millennium Labs., Inc., 923 F.3d 240, 244 (1st Cir. 2019) (“Millennium I”) (citing S. Rep. No. 99-3456, at 2 (1986)). It imposes civil liability upon anyone who knowingly presents, or causes to be presented, a false or fraudulent claim for payment or approval [or] knowingly makes, uses, or causes to be made or used, a false record or statement material to a false or fraudulent claim. 31 U.S.C. § 3729(a)(1)(A), (a)(1)(B). A “claim” is “any request or demand . . . . for money or property” presented to an officer, employee or agent of the United States. 31 U.S.C. § 3729(b)(2). The AKS imposes criminal liability on anyone who, inter

alia, knowingly and willfully offers or pays any remuneration (including any kickback, bribe, or rebate) directly or indirectly, overtly or covertly, in cash or in kind to any person to induce such person . . . . to purchase . . . . or arrange for or recommend purchasing . . . any good . . . . for which payment may be made in whole or in part under a Federal health care program[.] 42 U.S.C. § 1320a-7b(b)(2). A violation of the AKS which results in a federal health care payment is “per se [a] false claim under the FCA.” United States v. Regeneron Pharms., Inc., No. 20-11217, 2020 U.S. Dist. LEXIS 227643 at *43 (D. Mass. Dec. 4, 2020) (quoting Guilfoile v. Shields, 913 F.3d 178, 190 (1st Cir. 2019)). Private individuals can enforce the FCA as “relators” by bringing a civil qui tam action in the name of the government. Millennium I, 923 F.3d at 244. To bring a qui tam action under the FCA, a relator must file a complaint under seal, serve the government with a copy and provide it with all material evidence. Id. The government may intervene and proceed with the action or, if it does not, the relator may serve the complaint upon the defendant and litigate the action itself. Id. B. The Qui Tam Actions i. The Sanborn Complaint In October, 2017, relator Sanborn sued Athena in the

District of Massachusetts pursuant to the qui tam provisions of the FCA, alleging that Athena, an information technology company which specializes in the provision of healthcare services, had violated the FCA through the marketing and selling of its electronic health record (“EHR”) technology. EHR technology allows health care providers to record patient information electronically and provides essential support to the modern practice of medicine. Specifically, the relator complaint pled violations of the FCA related to 1) Athena’s “client referral incentive program” and 2) the noncompliance of its EHR technology with applicable federal certification criteria.

With respect to the client referral program, the relator complaint alleged that Athena’s customers were paid up to $3,000 per physician for referrals of new EHR customers. It further claimed that Athena provided other “gratuities and incentives” to induce sales of its EHR services, including tickets to sporting events, casino chips, hotel accommodations and meals. The complaint alleged that those payments and incentives violated the AKS and, because the government made payments through Medicaid and Medicare to healthcare providers who became Athena clients because of the incentive program, also violated the FCA. As to Athena’s EHR technology, the relator complaint

alleged that Athena marketed the technology with a guarantee that it would qualify its customers for incentive payments from the government pursuant to the American Recovery and Reinvestment Act of 2009, Pub. L. 111-5, 125 Stat. 115 (2009). To become eligible for incentive payments, a healthcare provider 1) had to possess certified EHR technology and 2) had to demonstrate meaningful use thereof. In 2015, the government reduced Medicare payments to healthcare providers who had not adopted certified EHR technology by 1%, followed by 2% and 3% reductions in 2016 and 2017, respectively. The relator complaint alleged that Athena’s EHR technology failed to meet applicable federal certification criteria. It

further claimed that, notwithstanding the failure, Athena deployed its EHR technology and made false representations regarding its compliance with federal regulations. As a result of those purported misrepresentations, the complaint alleged that Athena customers 1) received undeserved incentive payments and 2) were not penalized for failing to adopt certified and compliant EHR technology. ii. The McKusick and Lovell Complaint In December, 2017, relators McKusick and Lovell, unaware of Sanborn’s complaint which remained under seal, filed a qui tam

complaint against Athena. They alleged that Athena violated the FCA (and similar state statutes) through 1) “systemic, uncorrected flaws” in its billing systems that resulted in the submission of false and fraudulent claims for certain services, including home care services, 2) the failure to report and return the resulting overpayments to the government and 3) violations of the AKS (and similar state statutes) arising from incentive and kickback programs substantially similar those alleged in Sanborn’s complaint. C.

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Cite This Page — Counsel Stack

Bluebook (online)
United States of America v. AthenaHealth, Inc, Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-of-america-v-athenahealth-inc-mad-2022.