Simanski Ex Rel. O.A.S. v. Department of Health & Human Services

601 F. App'x 982
CourtCourt of Appeals for the Federal Circuit
DecidedFebruary 26, 2015
Docket2014-5077
StatusUnpublished
Cited by95 cases

This text of 601 F. App'x 982 (Simanski Ex Rel. O.A.S. v. Department of Health & Human Services) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Simanski Ex Rel. O.A.S. v. Department of Health & Human Services, 601 F. App'x 982 (Fed. Cir. 2015).

Opinion

HUGHES, Circuit Judge.

Todd Simanski and Julia Simanski appeal the United States Court of Federal Claims’s affirmance of a Special Master’s denial of compensation for their child, O.A.S., under the National Childhood Vaccine Injury Act. In certain cases, identifying the injury that is a basis for a claim under the Vaccine Act is a prerequisite to establishing causation of an injury by a vaccine. Because the Special Master did not act arbitrarily or capriciously by finding that the evidence shows that O.A.S. suffers from a disease for which the Si-manskis did not put forth a theory of causation, we affirm.

I

O.A.S. was born on November 2, 2000. Although she was diagnosed with intrauterine growth retardation and had decreased muscle tone for a newborn, she was otherwise healthy. At her two-month visit to her pediatrician, she was diagnosed with infectious gastroenteritis and her first set of scheduled vaccinations was deferred. On January 26, 2001, O.A.S. returned to the pediatrician and received doses of the diphtheria-tetanus-acellular pertussis, hepatitis B, Haemophilus influenzae type B, inactivated polio, and pneumococcal vaccines.

On January 30, 2001, O.A.S. went into respiratory arrest. After being rushed to Mercy Medical Center, she was intubated and placed on a ventilator. While at Mercy, she tested positive for respiratory syn-cytial virus (RSV) and she was initially diagnosed with bronchiolitis. During her stay at Mercy, doctors observed that O.A.S. was suffering from diaphragmatic palsy (or weakness), which is not a consequence of RSV. And twice the doctors were unable to remove her from the ventilator because she could not breathe independently. Doctors also observed that O.A.S. had staring episodes, arching of the back, and stiffening of the extremities.

In February 2001, O.A.S. was transferred to the Mayo Clinic for further diagnosis and treatment. While at the Mayo Clinic, O.A.S. received intravenous immu-noglobulin (IVIG) treatments, after which her health improved to the point where *984 she could breathe on her own. Doctors at the Mayo Clinic also performed many tests on O.A.S.’s blood, nerves, and neuromuscu-lar system. Based on the tests and their observations, doctors concluded that O.A.S. may have been suffering from sen-sorimotor peripheral neuropathy, i.e., impairment of the peripheral nerves, which are the nerves outside of the brain and spine. Other records from this time period suggested that O.A.S.’s doctors were also considering more specific diagnoses. For example, some medical records indicated “considering Guillain Barre [sic] syndrome,” “probable post-infectious demyeli-nating neuropathy,” weakness “consistent with a motor neuropathy or a sensorimotor axonal neuropathy,” and “not unlike axonal [Guillain-Barré Syndrome].” Respondent’s App. (R.A.) 113-14.

Guillain-Barré Syndrome (GBS) is a disease of unknown etiology that affects the peripheral nervous system. Doctors generally believe that GBS may begin through an autoimmune mechanism. The most common form, which the Simanskis allege O.A.S. may suffer from, is the demyelinat-ing type. Demyelinating-type GBS results in an impairment of sensorimotor signals traveling through the body’s nerves and is characterized by a degradation of myelin, a substance that covers peripheral nerves.

In March 2001, O.A.S. was transferred from the Mayo Clinic back to Mercy. Mercy records dated March 21, 2001 state that it was “probable” O.A.S. had GBS. R.A. 177. Although she was discharged from Mercy in late March, O.A.S. was readmitted in April 2001 due to respiratory failure. Test results during this stay at Mercy indicated that O.A.S.’s neurological condition was worsening. While at Mercy, O.A.S. was again placed on a ventilator. Since then, O.A.S. has required the permanent assistance of a ventilator.

In late April 2001, O.A.S. was transferred to Johns Hopkins University Hospital. Mercy’s discharge papers state that the “lack of a definitive diagnosis has been a problem in addressing the extent of supporting the child.” R.A. 86. Johns Hopkins records from April 2001 similarly indicate inconclusive diagnoses. One progress note states “post-infectious demyelinating neuropathy v. spinal muscular atrophy v. degenerative v. other [not otherwise specified].” R.A. 86. Nonetheless, doctors at Johns Hopkins concluded that O.A.S.’s condition was “consistent with either a motor neuropathy or a sensorimotor axonal neuropathy.” R.A. 86.

After her stay at Johns Hopkins, O.A.S. was transferred to the University of Iowa Hospital and she stayed there for over three months. In June 2001, O.A.S.’s treating physician recorded an improving clinical picture and after consulting a doctor from Atlanta, Georgia, noted that the Atlanta doctor “favors a diagnosis of an acute axonal neuropathy.” R.A. 183.

O.A.S. returned to Mercy in August 2001. Her diagnosis at admission was “flaccid axonal neuropathy.” She was discharged in September 2001.

In September 2003, following her pediatrician’s recommendation, O.A.S. returned to the Mayo Clinic for further evaluation. During this visit, Dr. Nancy Kuntz, a pediatric neurologist at the Mayo Clinic, began to question whether O.A.S. had spinal muscular atrophy with respiratory distress (SMARD). See R.A. 185 (quoting doctor’s note stating “[Question] SMARD”). SMARD is a genetic disease that can begin with the sudden onset of respiratory distress within the first thirteen months of life. This disease often involves diaphragmatic palsy and, like GBS, it involves dysfunction of the nervous system.

In one report, Dr. Kuntz wrote that her observations “suggestf ] progressive motor *985 and sensory neuronopathy or axonopathy. I believe that this is compatible with a recently described entity called SMARD. I believe that it would be very critical for us to confirm the diagnosis for [O.A.S.].” R.A. 185. Accordingly, Dr. Kuntz recommended that O.A.S. and her parents send genetic material to doctors who were investigating SMARD. Ultimately, the Simanskis did not send materials for genetic testing. Nonetheless, Dr. Kuntz diagnosed O.A.S. with SMARD.

The record indicates that from this point forward in O.A.S.’s life, doctors often, but not always, stated that O.A.S. had SMARD. In November 2003, O.A.S.’s pediatrician wrote a letter to an insurance company stating that O.A.S. had SMARD. In February 2004, a pediatric intensivist at Mercy summarized O.A.S.’s condition as “[k]nown neuromuscular disorder-SMA-RD type.” R.A. 186. In October 2004, O.A.S.’s pediatrician noted Dr. Kuntz’s diagnosis, but with the caveat that it had not yet been confirmed. And in 2004 and 2005, other treating doctors noted a neuro-muscular condition of unknown origin. Additionally, O.A.S.’s pediatric neurologist stated in January 2007 that O.A.S. had “a clinical diagnosis of sensorimotor axonal neuropathy that also can be called [SMARD].” R.A. 186. Similarly, in 2008, 2011, and 2012, other treating physicians assessed O.A.S. as having either spinal muscular atrophy or SMARD.

II

On January 17, 2003, the Simanskis filed a petition under the National Childhood Vaccine Injury Act of 1986, 42 U.S.C. §§ 300aa-l to -34, alleging that O.A.S.’s January 2001 vaccinations triggered adverse reactions.

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