William Taylor, Parent of Joseph Taylor, a Minor v. Secretary of Health & Human Services 0

108 Fed. Cl. 807
CourtUnited States Court of Federal Claims
DecidedFebruary 15, 2013
Docket05-1133V
StatusPublished
Cited by43 cases

This text of 108 Fed. Cl. 807 (William Taylor, Parent of Joseph Taylor, a Minor v. Secretary of Health & Human Services 0) 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
William Taylor, Parent of Joseph Taylor, a Minor v. Secretary of Health & Human Services 0, 108 Fed. Cl. 807 (uscfc 2013).

Opinion

Vaccine Act; Motion for Review of Special Master’s Decision; DTaP Vaccination; Infantile Spasms; Lack of Evidence of Causation; Althen Test.

OPINION AND ORDER

WHEELER, Judge.

This case comes before the Court on review of Special Master Dee Lord’s September 20, 2012 decision denying compensation to Petitioner, Joseph Taylor, through his father, William Taylor, under the National Childhood Vaccine Injury Act (“Vaccine Act”), 42 U.S.C. §§ 300aa-l et seq. Petitioner alleges that the Diphtheria-Tetanus-aeel-lular-Pertussis (“DTaP”) 2 vaccine Joseph received on December 5, 2003 “caused him to suffer an off-Table encephalopathy, a seizure disorder, and subsequent developmental delays.” Pet’r Br. 1. According to Respondent and the Special Master, Petitioner has failed to establish by a preponderance of the evidence that the DTaP vaccine caused his injury. The Court expresses its sympathy for the injuries that Joseph has endured, but for the reasons explained below, the Court affirms the Special Master’s decision.

Factual Background 3

Joseph Taylor was born to William and Audrey Taylor on June 10, 2003, and appeared healthy for the first six months of his life. On December 5, 2003, Joseph received the DTaP vaccine, the Inactivated Polio vaccine (“IPV”), the Haemophilus Influenzae type b (“Hib”) vaccine, and the Hepatitus B (“hep B”) vaccine. Later that day, Mrs. Taylor observed that Joseph seemed to be experiencing seizures, and took him to the Palomar Medical Center Emergency Room (“ER”) in Escondido, California. The record from this visit reflects that Joseph had a temperature of 100.1 degrees, and notes that Joseph received vaccinations earlier in the day. He had no episodes during the ER visit and had normal chest x-rays, urinalysis, and cultures, and a complete blood count. Joseph was discharged, and his parents were instructed to follow up with his pediatrician in 24 hours.

The following day, the Taylors noticed Joseph experiencing similar episodes, and took him to the Children’s Hospital in San Diego, as advised by the on-call doctor at their pediatrician’s office. Joseph experienced seizure episodes while at the hospital, and was admitted for a full evaluation. During the course of his hospital stay, Joseph underwent a series of tests: he had a normal M RI and echocardiogram, negative urine, blood, and CSF cultures, but a “markedly abnormal electroencephalogram [“EEG”] due to a pattern of electrical activity consistent with hyp-sarrhythmia.[ 4 ] Such findings may be associ *812 ated with infantile spasms.” Pet’r Ex. 6 at 252. Joseph continued to experience seizures and was started on adrenocorticotropic hormone (“ACTH”). His seizures decreased, and Joseph was discharged on December 12, 2003.

Joseph’s treating physicians diagnosed him with infantile spasms, also known as West Syndrome, a particular type of seizure disorder. Pet’r Ex. 6 at 294. In later years, Joseph continued to be treated by a child neurologist and receive ACTH therapy. He underwent physical, speech, and language therapy for developmental and gross motor delays, expressive language disorder, and hearing loss. Joseph was hospitalized for his seizures twice in 2006. The most recent medical recoi’ds indicate that Joseph has been clinically seizure free since February 2007, though he still has an abnormal EEG and a diagnosis of pervasive developmental delays.

Infantile spasms are a recognized epileptic condition. Resp’t Ex. C at 1; Tr. II 169. 5 The disorder of infantile spasms typically commences in infancy, with an average age of onset at six months. Resp’t Ex. C at 2. The disorder is characterized by a triad of a particular type of seizures, developmental retardation, and EEG abnormalities known as hypsarrhythmia. Pet’r Ex. 21 at 4. Infantile spasms are considered an epileptic encephalopathy, 6 which indicates that over a period of time, the seizing process results in subsequent mental deficits. Tr. II 46. Infantile spasms are frequently treated with ACTH, and although initial response to ACTH may be positive, relapses can, and often do, occur. Resp’t Ex. C at 11-13; Pet’r Ex. 22 at 4.

Much of the literature regarding infantile spasms includes classification systems, and during this ease, the parties devoted significant effort to addressing the various characterizations of infantile spasms. An earlier classification system categorized infantile spasms as idiopathic, cryptogenic, or symptomatic. Pet’r Ex. 31 at 2. Generally speaking, idiopathic and cryptogenic spasms are those of unknown origin or cause, and symptomatic spasms are those with identified causes of an abnormal brain condition. See id.; Resp’t Ex. I at 3. A more recent classification system categorizes infantile spasms as genetic, structural/metabolic, or unknown. Pet’r Ex. 31 at 2 n.l. Under this system, all symptomatic spasms would fall under “structural/metabolic,” and idiopathic and cryptogenic spasms would fall under either “unknown” or “genetic.” Id.

Both Petitioner’s and Respondent’s experts conceded, however, that at bottom, the classification systems are of little assistance in determining the cause of infantile spasms. When asked on cross-examination whether Joseph Taylor’s infantile spasms should be categorized under the older, or symptomatic/cryptogenic classification system, Petitioner’s expert, Dr. David Griesemer, responded:

Well, from my perspective that’s an irrelevant question because these are arbitrary, poorly defined boundaries to begin with. And when I’m meeting with a family, I don’t say, this is cryptogenic infantile spasms or this is symptomatic infantile spasms. I mean, it’s infantile spasms and either we do or don’t know what the cause of the problem is. This was a system that was identified a few decades ago in order to gather research data, I believe.

Tr. II 35. This testimony is consistent with Dr. Griesemer’s statement at an earlier hearing that “[t]here is no question that Joseph *813 Taylor could be placed in either group, cryp-togenic or symptomatic.” Tr. I 87. Similarly, Respondent’s expert, D r. Mary Anne Guggenheim, noted that it is the underlying cause of infantile spasms, and not the classification of the disorder, that determines a child’s eventual outcome. Resp’t Ex. 0 at 3.

History of Proceedings

Petitioner filed this Vaccine Act petition on October 19, 2005, alleging that the December 5, 2003 DTaP vaccine caused Joseph Taylor’s seizure disorder. The Office of Special Masters (“OSM”) assigned the ease to Special Master John Edwards, who held an entitlement hearing on March 16, 2007. Special Master Lord held a second entitlement hearing on October 25, 2011, and afforded the parties an opportunity to supplement the record with additional evidence. Petitioner’s and Respondent’s experts each provided four written expert reports. See Pet’r Exs. 13, 19, 31, 37; Resp’t Exs. A, I, O, U.

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