Galvan v. Secretary of Health and Human Services

CourtUnited States Court of Federal Claims
DecidedJanuary 11, 2021
Docket20-313
StatusPublished

This text of Galvan v. Secretary of Health and Human Services (Galvan v. Secretary of Health and Human Services) is published on Counsel Stack Legal Research, covering United States Court of Federal Claims primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Galvan v. Secretary of Health and Human Services, (uscfc 2021).

Opinion

In the United States Court of Federal Claims No. 20-313V Filed 1: January 11, 2021

ROSA SOTO GALVAN,

Plaintiff, Keywords: National Vaccine v. Injury Compensation Program, 42 SECRETARY OF HEALTH AND U.S.C. §§ 300aa-10 et seq. (2012); HUMAN SERVICES, Motion for Review; Arthrocentesis; Severity Requirement. Defendant.

Kristina K. Green, Kralovec, Jambois, & Schwartz, Chicago, IL, for Plaintiff.

Mary E. Holmes, Trial Attorney, Darryl R. Wishard, Assistant Director, Catherine E. Reeves, Deputy Director, C. Salvatore D’Allessio, Acting Director, and Ethan P. Davis, Acting Assistant Attorney General, Torts Branch, Civil Division, United States Department of Justice, Washington, D.C., for Defendant.

MEMORANDUM OPINION AND ORDER

TAPP, Judge.

In this vaccine case, Petitioner, Rosa Soto Galvan (“Galvan”), petitioned for compensation pursuant to the National Vaccine Injury Compensation Program, 42 U.S.C. §§ 300aa-10 et seq. (2012) (“Vaccine Act”), alleging that she suffered complications following the administration of various vaccinations. (Compl., ECF No. 1). Regarding the Vaccine Act’s severity requirement for remedies, Galvan alleged she experienced inpatient hospitalization and surgical intervention, specifically arthrocentesis—a procedure in which accumulated fluid is removed from a joint cavity by a needle. (Id. at 5). The Special Master reviewed Galvan’s claim, ultimately concluding that Galvan “cannot meet the statutory severity requirements pursuant to

1 This Order was originally filed under seal on December 17, 2020, (ECF No. 25). The Court provided parties the opportunity to review this opinion for any proprietary, confidential, or other protected information and submit proposed redactions no later than January 6, 2021. The parties did not file a status report indicating proposed redactions. In accordance with RCFC, App. B, Vaccine Rule 18(b)(2), “an objecting party must provide the court with a proposed redacted version of the decision. In the absence of an objection, the entire decision will be made public.” Thus, the sealed and public versions of this Order are identical, except for the publication date and this footnote. the Vaccine Act at § 300aa-11(c)(1)(D)” because “arthrocentesis, though an intervention, is not a surgical procedure.” (Galvan v. Sec’y of Health & Human Servs., No. 20-313V 2020 WL 4593163 (Fed. Cl. Spec. Mstr. July 6, 2020) at *1, *18, “Decision”, ECF No. 20). Consequently, on July 6, 2020, the Special Master granted Respondent, the Secretary of Health and Human Services’ (“the Secretary”), motion to dismiss pursuant to RCFC 12(b)(6).

On August 3, 2020, Galvan filed a Motion for Review, (ECF No. 22), before this Court arguing that the Special Master’s legal conclusions and attendant factual findings should be set aside as arbitrary, capricious, an abuse of discretion, or otherwise not in accordance with law. (Pet.’s Mot. for Rev., ECF No. 22-1 at 20). The sole issue before the Court is whether the Special Master’s conclusion is “arbitrary, capricious, an abuse of discretion, or otherwise not in accordance with law.” 42 U.S.C. § 300aa-12(e)(2)(B); RCFC, App. B, Vaccine Rule 27(b). As explained below, the Court finds that the Special Master’s decision was not arbitrary, capricious, or otherwise not in accordance with law. Therefore, the Court DENIES Galvan’s Motion for Review and AFFIRMS the Special Master’s decision.

I. Background

On September 26, 2018, Galvan received vaccines for Hepatitis A, Hepatitis B, Influenza, and Pneumococcal Conjugate (PVC 13). (Compl. at 2). Within one hour of the administration of these vaccines, Galvan experienced abdominal pain and chills, and within four hours, she experienced headache, nausea, vomiting, dizziness, chest pain and tightness, and tachycardia. (Id. at 2). The same day, Galvan presented at and was admitted to the Emergency Department at MacNeal Hospital in Berwyn, Illinois, where she would remain hospitalized until October 1, 2018. (Id. at 2). Shortly after arrival, Galvan developed a fever and an abnormal rhythm of sinus tachycardia. (Id. at 2–3). Thereafter, Galvan experienced swelling in her right knee and effusion, along with redness and blistering on the right arm at the site of the vaccine injection. (Compl. at 3, Ex. 4 at 220). Upon intake, Galvan was diagnosed with “other complications following immunization, not elsewhere classified” and her discharge diagnosis was “post-vaccination fever.” (Id. at 220, 222). During hospitalization, Galvan underwent arthrocentesis of her right knee, a procedure where a needle is injected into the knee to drain excess synovial fluid (i.e., effusion), thereby reducing swelling and pressure contributing to pain. (Compl. at 3; see Compl., Ex. 4 at 220; Pet.’s Mot. for Rev. at 6). A rheumatologist performed the arthrocentesis. (Pet.’s Ex. 5 at 3, ECF No. 17-1).

Galvan petitioned for vaccine compensation on March 20, 2020, claiming that arthrocentesis constitutes a surgical procedure caused by her vaccine injury and that she was entitled to compensation under the Vaccine Act. (See generally Compl.). The Secretary moved for dismissal pursuant to RCFC 12(b)(6), arguing that Galvan’s claim failed to satisfy the Vaccine Act’s severity requirement. (Mot. to Dismiss, ECF No. 13). The Special Master found that arthrocentesis, though an intervention, is not a surgical intervention and granted the Secretary’s Motion to Dismiss. (Decision at *1).

In 1986, Congress passed the Vaccine Act, establishing a program administered by the Secretary of Health and Human Services to increase the safety and availability of vaccines. 42 U.S.C. § 300aa-1; Terran v. HHS, 195 F.3d 1302, 1307 (Fed. Cir. 1999). The Vaccine Act created the National Vaccine Injury Compensation Program, through which claimants could

2 petition for compensation due to alleged vaccine-related injuries or death. 42 U.S.C. § 300aa- 10(a). Under the Vaccine Act, there are two methods by which a petitioner may demonstrate eligibility for an award. A petitioner may demonstrate with reliable medical evidence that an injury listed on the Vaccine Injury Table occurred within the requisite period or that an unlisted injury was caused-in-fact by a vaccine listed on the Table. 42 C.F.R. § 100.3; 42 U.S.C. § 300aa-11(c)(1)(C). In either instance, the Vaccine Act imposes a “severity requirement” on petitioners. A petitioner must prove that the individual experiencing the alleged vaccine-related injury: (i) suffered the residual effects or complications of such illness, disability, injury, or condition for more than 6 months after the administration of the vaccine, or (ii) died from the administration of the vaccine, or (iii) suffered such illness, disability, injury, or condition from the vaccine which resulted in inpatient hospitalization and surgical intervention.

42 U.S.C. § 300aa-11(c)(1)(D) (severity requirement). The underlying Motion to Dismiss was predicated on whether Galvan met the requirement for “surgical intervention,” as it applies to the severity requirement.

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