Stone v. Secretary of the Department of Health & Human Services

99 Fed. Cl. 187, 2011 U.S. Claims LEXIS 976, 2011 WL 2160885
CourtUnited States Court of Federal Claims
DecidedMay 19, 2011
DocketNo. 04-1041V
StatusPublished
Cited by11 cases

This text of 99 Fed. Cl. 187 (Stone v. Secretary of the Department of Health & 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
Stone v. Secretary of the Department of Health & Human Services, 99 Fed. Cl. 187, 2011 U.S. Claims LEXIS 976, 2011 WL 2160885 (uscfc 2011).

Opinion

OPINION

MARGOLIS, Senior Judge.

This matter comes before the Court on a motion for review, filed February 22, 2011 by petitioners Jennifer and Gary Stone, as parents and next friends of Amelia Stone, a minor, seeking reversal of Special Master Gary J. Golkiewicz’s decision on remand (“Dec. on Remand”), filed January 20, 2011, denying petitioners’ request for compensation under the National Vaccine Injury Compensation Program, 42 U.S.C. § 300aa-10, et seq. (the “Vaccine Act”). Because the special master applied the correct legal standards and was neither arbitrary nor capricious in his factual findings, the decision is affirmed.

I. Background

Amelia Stone received a DTaP1 vaccination on August 27, 2001, shortly after her [189]*189birth on April 17, 2001. (See Decision of Special Master Golkiewicz at 4, Apr. 15, 2010 (“Dec.”).) Shortly after receiving the vaccination, Amelia experienced two severe seizure episodes. (See id. at 4-5.) Amelia was subsequently diagnosed with SMEI, a “particular epilepsy syndrome” that “begins in the first year of life in previously healthy children” and may result in “long lasting [seizures] ... associated with fever.” (Id. at 2 n. 2.) “SMEI” stands for “Severe Myo-clonic Epilepsy of Infancy,” also known as “Dravet Syndrome.” (Id.) As a result of her SMEI, Amelia continued to experience seizures, which have led to developmental delay. (See id. at 5-6.)

Amelia’s parents filed a petition for compensation on Amelia’s behalf under the Vaccine Act. At trial, respondent, the Secretary of the Department of Health and Human Services, relied on testimony from Dr. Gerald Raymond, a pediatric neurologist and geneticist. (See id. at 13.) Dr. Raymond testified that: “Amelia’s vaccinations neither caused nor exacerbated her SMEI, but rather a mutation in her SCN1A gene is solely responsible for her SMEI.” (Id. at 18.) Petitioners relied on testimony from Dr. Marcel Kinsbourne, a neurologist. (See id. at 11.) Dr. Kinsbourne acknowledged that “the SCN1A gene mutation plays a role in Amelia’s SMEI,” but claimed that the vaccine “triggered the onset of her Dravet syndrome” by “lowering] her seizure threshold.” (Id. at 40.) After hearing the parties’ testimony and arguments, the special master found in favor of respondent and entered an order denying compensation. (See id. at 51-52.)

This Court subsequently reversed the order on October 28, 2010, holding that the special master failed to apply the correct legal standard for causation. (See Order on Mot. for Review.) On remand, the special master once again denied compensation, finding that respondent had “prove[n] by a preponderance of the evidence that the SCN1A gene mutation was the sole cause and that it was principally responsible for Amelia’s SMEI.”2 (Dee. on Remand at 2.)

II. Standard of Review

The Court “owe[s] no deference to the ... special master on questions of law;” such questions are subject to de novo review. Broekelschen v. Sec’y of Health & Human Servs., 618 F.3d 1339, 1345 (Fed.Cir.2010). However, the Court must “uphold the special master’s findings of fact unless they are arbitrary and capricious.” Id. The Court does not “reweigh the factual evidence, or [] assess whether the special master correctly evaluated the evidence,” nor does the Court “examine the probative value of the evidence or the credibility of the witnesses.” Id. at 1349 (quoting Munn v. Sec’y of Health & Human Servs., 970 F.2d 863, 871 (Fed.Cir.1992)). “[If] the Special Master’s conclusion [is] based on evidence in the record that [is] not wholly implausible, [the Court is] compelled to uphold that finding as not being arbitrary or capricious.” Cedillo v. Sec’y of Health & Human Servs., 617 F.3d 1328, 1338 (Fed.Cir.2010) (quoting Lampe v. Sec’y of Health & Human Servs., 219 F.3d 1357, 1363 (Fed.Cir.2000)). Moreover, “[t]he special master’s decision often times is based on the credibility of the experts and the relative persuasiveness of their competing theories;” the special master’s findings with respect to expert credibility “are virtually unchallengeable on appeal.” Broekelschen, 618 F.3d at 1347 (quoting Lampe, 219 F.3d at 1362).

III. Analysis

A. SCN1A Mutation as the Sole Substantial Cause of Amelia’s SMEI

Petitioners argue that relevant medical literature and Dr. Raymond’s admissions show that the knowledge necessary to make a prediction about the effects of Amelia’s SCN1A mutation does not exist. Respondent argues that it presented reliable, preponderant evidence which established [190]*190that a factor unrelated was responsible for Amelia’s SMEI.3

As a threshold matter, petitioners take issue with Dr. Raymond’s qualifications, arguing that he is “not an SCN1A expert,” “[n]or is he an expert in epilepsy.” (Mot. at 29 (emphasis in original).) Dr. Raymond is, however, “an associate professor of neurology at Johns Hopkins University and the director of neurogenetics at the Kennedy Kreiger Institute, an affiliate of Johns Hopkins medical School.” (Dec. at 13.) Further, Dr. Raymond “performs consulting services in genetics at ... Johns Hopkins,” and “provides genetics counseling and consultation to families in relation to the results of genetics tests.” (Id.) Based on these credentials, the special master was not arbitrary or capricious in determining that Dr. Raymond was qualified to testify on the relationship between Amelia’s SCN1A mutation and her SMEI. (Id.) See SEB S.A. v. Montgomery Ward & Co., Inc., 594 F.3d 1360, 1373 (Fed.Cir.2010) (noting “wide latitude” in admitting expert testimony, affirming eourt’s ruling where there was an “adequate relationship” between expert’s experience and issues).

Next, petitioners disagree with the substance of Dr. Raymond’s conclusions, citing three reasons why there is insufficient evidence of the proposed relationship between Amelia’s SCN1A mutation and her SMEI.

First, petitioners complain that “the SCN1A variant that Amelia Stone has is both novel and unstudied.” (Mot at 29 (emphasis in original).) Dr. Raymond “agreed [with petitioners] ... that evidence of Amelia’s specific genotype-phenotype4 does not currently exist.” (Dee. at 33.) However, Dr. Raymond explained that “similar mutations in nearby areas [of the relevant gene] are documented,” and “[t]he phenotype for these reported mutations is predominantly SMEI.” (Id.) Moreover, Dr. Raymond was able to infer the genotype-phenotype relationship from a number of factors that, “when examined by a geneticist, cumulatively demonstrate that Amelia’s SMEI is caused by her SCN1A mutation.” (Id. at 26 (emphasis in original).) Dr.

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99 Fed. Cl. 187, 2011 U.S. Claims LEXIS 976, 2011 WL 2160885, Counsel Stack Legal Research, https://law.counselstack.com/opinion/stone-v-secretary-of-the-department-of-health-human-services-uscfc-2011.