# Rudzki v. Secretary of Health and Human Services

> United States Court of Federal Claims · June 15, 2026

URL: https://www.frixlaw.com/law-library/cases/11343331

## Case

- **Court:** United States Court of Federal Claims
- **Decided:** June 15, 2026
- **Precedential status:** Unpublished
- **Opinion:** Opinion
- **Judges:** Mindy Michaels Roth
- **Cited by:** 0 later opinions in the Frix Law Library

## Citator (automated)

- No negative treatment found by the automated citator. That is not the same as a confirmation that the case is good law; read the citing cases.
- Full citator and citing cases: https://www.frixlaw.com/law-library/cases/11343331

## Opinion text

In the United States Court of Federal Claims
OFFICE OF SPECIAL MASTERS
No. 18-617V
Filed: May 19, 2026

* * * * * * * * * * * * * * * * * * *
JEANNE RUDZKI, *
*
Petitioner, *
*
v. *
*
SECRETARY OF HEALTH *
AND HUMAN SERVICES, *
*
Respondent. *
*
* * * * * * * * * * * * * * * * * * *

Bridget McCullough, Esq., Muller Brazil, LLP, Dresher, PA, for petitioner.
Mallori Openchowski, U.S. Department of Justice, Washington, DC, for respondent.

DECISION 1

Roth, Special Master:

On May 1, 2018, Jeanne Rudzki (“Ms. Rudzki” or “petitioner”) timely filed a petition for
compensation under the National Vaccine Injury Compensation Program, 42 U.S.C. § 300aa-10,
et seq. 2 (“Vaccine Act” or “Program”). Petitioner alleges that she suffered “chronic encephalitis
resulting from the [Tdap] vaccination, a ‘Table’ injury, which is contained on the Vaccine Injury
Table, 42 C.F.R. 100.3 (a) II (B) 2017, received on December 5, 2015. Petitioner’s symptoms
began within seventy-two (72) hours of vaccination and lasted for more than six (6) months.” 3
Petition at 1, ECF No. 1.

1
Because this Decision contains a reasoned explanation for the action taken in this case, it must be made publicly
accessible and will be posted on the United States Court of Federal Claims' website, and/or at
https://www.govinfo.gov/app/collection/uscourts/national/cofc, in accordance with the E-Government Act of 2002.
44 U.S.C. § 3501 note (2018) (Federal Management and Promotion of Electronic Government Services). This means
the Decision will be available to anyone with access to the internet. In accordance with Vaccine Rule 18(b), Petitioner
has 14 days to identify and move to redact medical or other information, the disclosure of which would constitute an
unwarranted invasion of privacy. If, upon review, I agree that the identified material fits within this definition, I will
redact such material from public access.
2
National Childhood Vaccine Injury Act of 1986, Pub. L. No. 99-660, 100 Stat. 3755 (1986). Hereinafter, for ease of
citation, all “§” references to the Vaccine Act will be to the pertinent subparagraph of 42 U.S.C. § 300aa (2018).
3
The terms “encephalitis” and “encephalopathy” are used interchangeably throughout this Decision because
petitioner’s providers used both terms. Encephalopathy is defined as any degenerative disease of the brain, while
encephalitis is defined as inflammation of the brain. Encephalopathy, DORLAND’S ILLUSTRATED MEDICAL
DICTIONARY 608 (33rd ed. 2020) [hereinafter Dorland’s]; Encephalitis, Dorland’s at 605.

1
For the detailed reasons set forth below, I find that petitioner has not demonstrated by
preponderant evidence that the Tdap vaccination she received on December 5, 2015 caused
encephalitis or played any role in her seizures later diagnosed as epilepsy. Thus, she is not entitled
to compensation.

I. Procedural History

The petition was filed on May 1, 2018, in addition to some of petitioner’s medical records.
Petitioner’s Exhibits (“Pet. Ex.”) 1-5, ECF No. 1. The case was assigned to the undersigned the
following day. ECF No. 4.

Petitioner filed additional medical records on May 31, 2018 and a statement of completion
on June 1, 2018. Pet. Ex. 6, ECF Nos. 7-8. Following several extensions, respondent filed a status
report on February 5, 2019, identifying records that remained outstanding. ECF Nos. 9-12, 14.

Petitioner filed additional records on March 7, 2019 and April 2, 2019. Pet. Ex. 7-8, ECF
Nos. 16-18. Respondent filed his Rule 4(c) Report on July 25, 2019, advising that this case was
not appropriate for compensation. ECF No. 22.

Petitioner filed an expert report from Dr. Frederick Nahm on November 22, 2019. Pet. Ex.
9, ECF No. 25. Respondent filed a responsive expert report from Dr. Steven Evans on April 20,
2020. Respondent’s Exhibit (“Resp. Ex.”) A, ECF No. 30. Petitioner filed another report from Dr.
Nahm on July 15, 2020, and respondent filed another report from Dr. Evans on September 24,
2020. Pet. Ex. 20, ECF No. 34; Resp. Ex. C, ECF No. 36.

A status conference was held on January 25, 2021. A detailed Order was issued thereafter
memorializing the discussions, which included the content of petitioner’s medical records, the
expert reports filed by both parties, and several issues that needed to be addressed prior to
entitlement, one being that petitioner’s only claim was for “chronic encephalitis resulting from a
[Tdap] vaccination, a ‘Table’ injury.” Petition at 1. Notably, it was discussed that the concern
raised for encephalitis in the medical record was ruled out by lumbar puncture and paraneoplastic
antibody panel, both being normal. Therefore, there was no support for petitioner’s Table claim of
encephalitis. Further, the medical records included petitioner’s reports of what appeared to be prior
symptoms of seizure activity before her receipt of the subject Tdap vaccination. It was determined
that a fact hearing would be necessary prior to proceeding to entitlement and was scheduled for
December 9, 2021. ECF Nos. 38, 40.

At the time of the pre-hearing conference on December 3, 2021, I noted concern that the
medical records as filed were incomplete. After further discussion, the fact hearing was adjourned,
and a deadline was set for petitioner to file the outstanding records. ECF Nos. 43-44.

Medical records were filed on January 13, 2022, February 14, 2022, March 16, 2022, April
14, 2022, and May 16, 2022. Pet. Ex. 27-40, ECF Nos. 45-53. Petitioner also filed a letter from
her treating neurologist, Dr. Tiffany Eady, on February 14, 2022. Pet. Ex. 32, ECF No. 47.

2
A status conference was held on June 9, 2022. An Order issued after the conference,
detailing the recent records filed which showed that petitioner’s complaints following her receipt
of the Tdap vaccination were the same as her complaints prior to receiving the subject vaccination,
including experiencing auras and absence episodes. Petitioner’s claim that she suffered a Table
encephalitis when encephalitis had been ruled out by objective testing was again questioned. Also
discussed was the finding on MRI that petitioner had a congenital brain anomaly of cortical
dysplasia known to cause epilepsy. ECF No. 55.

Petitioner filed additional records on July 10, 2022. Pet. Ex. 41-44, ECF Nos. 60, 65.
Respondent then identified more records that appeared outstanding. ECF No. 68. Petitioner filed
those records on December 5, 2022. Pet. Ex. 45-49, ECF No. 70.

Another status conference was held on February 2, 2023 to discuss the more recently filed
medical records. Petitioner’s history of absence episodes, sleep disturbances which included
tossing in her bed and tearing the sheets, and the finding of cortical dysplasia on MRI were
discussed. It was noted that “more than 24% of epilepsies are due to cortical dysplasia, and medical
literature supports that those with cortical dysplasia develop epilepsy at some point in adulthood
and when they do, it is generally after some trigger.” Thus, this case was a significant aggravation
claim, and petitioner needed an expert report to address adult onset of epilepsy in the context of
cortical dysplasia and petitioner’s clinical history. ECF No. 71 (citations omitted).

On April 25, 2023, petitioner filed an expert report from one of petitioner’s treating
physicians, Dr. Fawad Khan, along with medical literature. Pet. Ex. 50-65, ECF No. 73.
Respondent filed a responsive report on July 26, 2023. Resp. Ex. D, ECF No. 75. Petitioner
confirmed she would not be filing any further reports and requested a Rule 5 Conference. ECF
Nos. 76-77.

A Rule 5 Conference was held on November 15, 2023. The expert reports were discussed,
and settlement was encouraged with the filing of a Motion for Ruling on the Record if a settlement
could not be reached since the record was well-developed. ECF No. 79.

On January 15, 2024, petitioner advised that she would prefer to proceed with a Ruling on
the Record and would “not be using Dr. Nahm’s opinion to support her motion.” ECF No. 80. A
briefing schedule was set.

Petitioner filed her Motion on April 19, 2024, maintaining that she was entitled to
compensation “for encephalitis, a ‘Table injury,’ resulting from the [Tdap] vaccination she
received on December 5, 2015.” Motion, ECF No. 82. Respondent responded on August 2, 2024.
Response, ECF No. 85. Petitioner did not file a reply.

This matter is now ripe for ruling.

II. Relevant Terminology

The following medical terms appear throughout this decision and the medical records.

3
Seizure is defined as the sudden attack or recurrence of a disease or the single episode of
epilepsy. An absence seizure consists of a sudden momentary break in consciousness of thought
or activity, sometimes accompanied by automatisms or clonic movements, especially of the
eyelids. Focal seizure, also referred to as a partial seizure, is any seizure due to a lesion in a
specific, known area of the cerebral cortex. Dorland’s at 1660.

A simple partial seizure is associated with autonomic and/or psychic symptoms and
sensory phenomena such as olfactory and auditory. Resp. Ex. A Tab 1 at 2. 4 Complex partial
seizure is a partial seizure characterized by varying degrees of impairment of consciousness; the
person affected performs non-purposeful, repetitive movements which they may not remember.
They usually begin with motor arrest and are followed by post-ictal confusion and amnesia. Id.;
Dorland’s at 1660.

Epilepsy is characterized by paroxysmal transient disturbances of brain function that may
manifest as loss of consciousness, abnormal motor phenomena, sensory disturbances, or
perturbation of the autonomic nervous system. Dorland’s at 626.

Grand mal epilepsy is a symptomatic form of epilepsy often preceded by an aura and
characterized by loss of consciousness with generalized tonic-clonic seizures. Dorland’s at 626.

Temporal lobe epilepsies are characterized by simple partial seizures, complex partial
seizures, and secondarily generalized seizures, or a combination of all of these. Resp. Ex. A Tab 1
at 2. 5 Seizures in temporal lobe epilepsies generally occur in clusters at intervals or randomly. Id.
EEG findings in temporal lobe epilepsies may show no abnormality; slight or marked asymmetry
of background activity; or temporal spikes, sharp waves, and/or slow waves that are unilateral or
bilateral, synchronous or asynchronous, and may not be always localized to the temporal region.
Id.; Dorland’s at 627.

Focal cortical dysplasia (“FCD”) is a term used to describe a large spectrum of lesions
increasingly recognized as a cause of medically refractory epilepsy. It can be in any part of the
cortex and may affect multiple lobes. Pet. Ex. 22 at 2; 6 Resp. Ex. A Tab 16 at 2. 7 On neuroimaging,
FCD findings include increased cortical thickness, blurring of the cortical-white matter junction,
increased signal on T2-weighted images, and cortical thinning. Pet. Ex. 22 at 3. FCD typically
presents in children but can begin in adulthood. Resp. Ex. A Tab 16 at 1. The most common seizure
type in FCD is complex partial seizures. Id.

III. Factual Background

A. Medical History Prior to the Subject Vaccine

4
Commission on Classification and Terminology of the International League Against Epilepsy, Proposal for Revised
Classification of Epilepsies and Epileptic Syndromes, 30 Epilepsia 389 (1989), filed as “Resp. Ex. A Tab 1.”
5
Id.
6
Ingmar Blumcke et al., The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification
proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission, 52 Epilepsia 158 (2011), filed as
“Pet. Ex. 22.”
7
A.M. Siegel et al., Adult-onset epilepsy in focal cortical dysplasia of Taylor type, 64 Neurology 1771 (2005), filed
as “Resp. Ex. A Tab 16.”

4
The primary care records begin in 2014. Petitioner’s past medical history included but was
not limited to pernicious anemia, vitamin D deficiency, insomnia, joint pain, fatigue, and malaise.
Pet. Ex. 4 at 10-11, 14-15, 20-22.

Petitioner presented to her primary care physician (“PCP”) Dr. Short on October 27, 2015,
with “some problems lately.” Pet. Ex. 4 at 20. She was 63 years old, reporting fatigue, waking in
the morning having “really kicked her sheets everywhere . . . to the point now that they actually
have tears in them”, snoring a lot, waking not feeling rested, and feeling restless. Id. She was noted
to have joint pain, insomnia, and fatigue. Id. at 21. Dr. Short’s assessment included concerns for
sleep problems causing fatigue, “some myoclonus[ 8] which is a sleep disorder”, and “some sleep
apnea symptoms” requiring a sleep study. Id. at 22-23, 26. Petitioner received a quadrivalent
influenza vaccine at this visit. Id. at 23, 34.

Petitioner received the subject Tdap vaccine on December 5, 2015 at Walgreens. Pet. Ex.
1 at 8-9.

B. Petitioner’s Medical History After the Subject Vaccine

On December 8, 2015, petitioner was involved in a single vehicle accident while driving.
She was transported to University Hospital by EMS, 9 who noted that her side airbag deployed,
there was no visible head trauma or hematoma, and no known loss of consciousness. She was
speaking in full sentences but was disoriented to time and year. She did not recall crashing her car.
Pet. Ex. 2 at 8. She was evaluated by a nurse and ER resident, who noted at that time she was
oriented to time and place and reported that she “has been suffering ‘seizures sitting and staring
spells’ for past year. Has not seen a doctor.” Id. She described these episodes as staring off, but
she can still move and talk, just “feels slower.” Id. at 10.

Petitioner suffered a seizure witnessed by her daughter while in the ER. She became
confused, was unable to answer questions, began to shake, and was then post-ictal. She was given
Ativan. A head CT was ordered. Pet. Ex. 2 at 12. Her daughter reported several similar episodes
of unresponsiveness in the past year, described as staring off, not responding, without tonic/clonic
movements, atonia, foaming at the mouth, or incontinence. The differential at that point included
undiagnosed seizure disorder, among other conditions. Id. A neurology consult was ordered. Id. at
12-13.

Petitioner was taken for a head CT at which time the radiology technician reported a 1-2-
minute episode of seizing with white foamy oral discharge. She was unable to communicate with
staff and was then snoring audibly. Another 2mg of Ativan was administered. When next
evaluated, she was oriented to time and place but did not recall the seizure event. She felt “drowsy.”
Pet. Ex. 2 at 9. Physical examination was normal. Id. at 11. There was no intracranial abnormality
on CT. Id. at 14. A chest x-ray revealed a right posterior medial 10th rib fracture. Id. at 14-15.

8
Myoclonus refers to shock-like contractions of a portion of a muscle, an entire muscle, or a group of muscles,
restricted to one area of the body or appearing synchronously or asynchronously in several areas. Dorland’s at 1205.
9
The police report and EMS records were not filed.

5
Petitioner was loaded with Keppra in the ER and discharged home on oral Keppra. She
was instructed not to drive, avoid alcohol, and follow up with neurology. Pet. Ex. 2 at 13.
Information on seizures and rib fractures was provided. Id. at 38-42.

Petitioner presented to Dr. Helmstetter the next day, December 9, 2015, reporting her
involvement in a motor vehicle accident yesterday morning secondary to seizure while exiting the
parkway and hitting the guardrail. She was wearing a seatbelt. The side airbag deployed. It was
unclear if she sustained any head trauma. She had no memory of the accident. She was seen in the
ER, and a head CT was normal, but she sustained a rib fracture. She reported a “grand mall (sic)
seizure while in the ER” but denied any history of seizures. Pet. Ex. 3 at 80. Keppra was prescribed.
She denied confusion, headaches, vision changes, or history of any cardiovascular event. Id. She
had mild bilateral shoulder pain with full range of motion of both shoulders and myalgias. The
remainder of the examination was normal. Id. at 80-81. The assessment was unspecified
convulsions, motor vehicle accident, rib fracture, and shoulder pain. Id. at 81. She was to continue
taking Keppra. Id.

On December 11, 2015, petitioner presented to Dr. Hightower at SCPC Neurology. Her
“problems” were listed as convulsions; partial symptomatic epilepsy with complex partial seizures,
not intractable, without status epilepticus; seizure disorder, generalized convulsive, intractable;
and anxiety. Pet. Ex. 3 at 84. Petitioner was being evaluated for “blacking out while driving” on
December 8, 2015. Id. at 91. She reported losing consciousness while getting off at an exit, and
the next thing she remembered was waking in an ambulance and then again in the ER. Id. She had
another seizure while in the ER with her daughter, who reported foaming at the mouth, gurgling,
and reaching for things in the air, for her blanket, and for the nurses, which lasted about 45 seconds
with urinary incontinence. Id. at 92. Ativan was given after the seizure stopped. Petitioner reported
that she had episodes of “déjà vu” for the past year, once a month or every other month. Her
daughter witnessed an episode and reported that she stopped talking mid-conversation and when
asked if she was having “an episode,” petitioner nodded yes but could not speak for about 30
seconds. Petitioner reported that “[t]he last episode of this déjà vu feeling was Tuesday morning
the same day she had two seizures.” Petitioner described the episodes as wanting to talk but being
unable to speak. She denied head trauma. She reported a febrile convulsion at age 2. Her son also
had a febrile seizure at age 2. A head CT was negative. She was taking Keppra without side effects.
Id. She reported still feeling confused with memory loss since the episodes on Tuesday with
dizziness and anxiety. She had received a Tdap the Saturday before. Id.

Petitioner presented for her first brain MRI and EEG on December 24, 2015. Pet. Ex. 3 at
106. The MRI revealed abnormal edema signal with fullness within the left insula and left mesial
temporal lobe with a suggestion of additional edema on the right insula and mesial temporal lobe.
The findings were interpreted as related to seizure activity given her history, but encephalitis could
not be excluded so clinical correlation with CSF analysis was recommended. Pet. Ex. 3 at 106-07.
“Expanded differential includes limbic encephalitis.” Id. at 107. The EEG performed the same day
was “mildly abnormal [] with left temporal slowing . . . nonspecific and most often associated with
vascular disease. No epileptiform potentials or electrographic seizures are identified at this time,
however.” Id. at 112-13.

6
A lumbar puncture (“LP”) also performed on December 24, 2015 was normal with no
infection found, a white blood cell (“WBC”) count of 1 (normal), and only mildly elevated protein
at 45, reference range of 15-40 mg/dL. Pet. Ex. 3 at 11, 15, 18, 122, 125. The discharging physician
wrote that petitioner “appear[ed] remarkably well,” and there was “low clinical suspicion for acute
infectious etiology.” Id. at 10. She was to follow up with neurology. Id. at 121.

In an email from neurologist Dr. Elkayam on December 29, 2016, petitioner was advised
that some results on LP were still pending, but it was doubtful the seizures were related to an
infection. Additionally, the “EEG does not show herpes in the brain.” Pet. Ex. 3 at 137. On
December 31, 2015, Dr. Elkayam advised petitioner that the CSF results showed no infection or
cancer cells. Id. at 140.

Petitioner presented to Dr. Elkayam on January 6, 2016. She was previously seen by Dr.
Hightower. Her first seizure was unwitnessed and resulted in a motor vehicle accident, and the
second was witnessed in the ER by her daughter. Pet. Ex. 3 at 157. Dr. Elkayam received the MRI
results; due to a question of viral encephalitis, an LP for CSF was ordered. “The cytology of the
CSF, white blood cell count, CMV/HSV/Lyme’s/RPR/West Nile are negative/unremarkable. The
protein was slightly elevated. Her EEG showed some focal slowing [] consistent with the MRI
findings, but no evidence of periodic complexes, epileptiform activity.” Id. This was explained to
petitioner and her daughter. Id. Dr. Elkayam’s assessment was abnormal brain MRI, seizure
disorder, and unspecified convulsions. Id. at 160, 167. The plan was to repeat the EEG and MRI,
as well as order a paraneoplastic serum antibody panel to test serology for anti-Hu, anti-Ma2, and
anti-NMDAR antibodies. Id. at 157, 161. She was allowed to drive if she took the Keppra. Id.

In an email to Dr. Elkayam on January 9, 2016, petitioner questioned whether the Tdap
vaccination was the cause of her seizures. Pet. Ex. 3 at 176. Dr. Elkayam’s response included only
that the paraneoplastic panel antibodies were normal, and she did not have to return but should see
Dr. Ramsay, who was a seizure specialist. Id. at 182, 211-212, 255.

Repeat brain MRI and EEG were performed on January 11, 2016. The MRI revealed near
normal findings with the prior abnormal fullness and edema signal within the left mesial temporal
lobe almost resolved. Pet. Ex. 3 at 175, 185-86. The repeat EEG was mildly abnormal with
background frequencies a little slower than expected for an adult, indicating a mild nonspecific
and non-focal encephalopathy. The clinical correlation was “mild nonfocal cortical dysfunction,
which could be related to a metabolic or toxic process and also could be late residual of a
convulsion.” Id. at 192.

Petitioner sent an email to Dr. Short on January 16, 2016 about an “adverse reaction to the
Tdap shot” and “grand mal seizure” in her car within 72 hours of vaccination with another grand
mal seizure while in the ER, abnormal MRI concerning for herpes encephalitis, and lumbar
puncture that “tested for everything from cancer cells to Lyme, West Nile, herpes encephalitis, and
even syphilis of the brain”, and “[e]verything came back clear except for a slightly elevated protein
level.” Petitioner added that she never had a seizure before in her life. Petitioner questioned
whether she should get the shingles vaccine. Pet. Ex. 4 at 43. A response from Dr. Short’s office
included that it “sounds like a viral meningitis but that [it’s] not from the vaccine and that it goes
away.” Id. Petitioner was also advised to not receive the shingles vaccine at this time. Id.

7
Petitioner sent another message to Dr. Elkayam on February 3, 2016, advising that she was
submitting a VAERS report and recently experienced “night and day” of déjà vu episodes but was
doing well and back to volunteering. Pet. Ex. 3 at 244.

Petitioner presented to Dr. Ramsay for consultation on April 28, 2016. She provided her
history which included insomnia and taking two Tylenol PM tablets nightly for 8 years. Pet. Ex. 3
at 256-57. She had a “DPT” vaccine 5 days prior to seizures. Id. at 257. Dr. Ramsay discussed her
prior test results. Id. at 257, 259-60. Neurological examination was normal. Id. at 262-63. His
impression was “DPT reaction producing mild mesial temporal edema which has improved”,
insomnia, and “[p]rovoked seizure – the temporal relationship of the DPT shot and the seizure and
the MRI changes suggest the seizure was from a reaction to the DPT. Follow up MRI showed
resolution of the changes.” Id. at 263. An ambulatory 48-hour EEG and MRI with epilepsy protocol
were ordered. Keppra was to continue. Id.

Repeat MRI performed on May 3, 2016 revealed no definite abnormalities or significant
detrimental changes when compared to the prior MRI. Pet. Ex. 3 at 281-82. The previously-
visualized abnormal fullness and edema within the left mesial temporal lobe and insula was largely
resolved. Id.

A 48-hour ambulatory EEG was ordered by Dr. Khan on referral from Dr. Ramsay on May
4, 2016 to assess for underlying epilepsy. Dr. Khan’s impression was “abnormal EEG during
wakefulness, drowsiness and sleep. Independent left and right temporal focal polymorphic delta
range slowing was noted. Left temporal slow wave complexes were noted. Left temporal sharp
waves were also noted.” Pet. Ex. 3 at 287-89. Dr. Khan’s “clinical correlation” included a 63-year-
old female with “a history of generalized seizures following vaccination.” Id. at 289. The findings
on 48-hour EEG were previously reported on EEG in December of 2015. The left temporal sharp
waves confer an increased risk of focal seizures from this region. No seizures were recorded during
the study. Id.

Petitioner sent an email to Dr. Ramsay on May 28, 2016, describing feelings of “doom and
dread”, and believed the Keppra was causing anxiety. Pet. Ex. 3 at 327. Dr. Ramsay phoned
petitioner who reported feeling better. She was told to try melatonin for sleep rather than the
Benadryl (Tylenol PM) she was taking. Id. at 330.

Petitioner returned to Dr. Ramsay on June 27, 2016. His impressions remained unchanged.
Pet. Ex. 3 at 335, 339, 348. Her test results indicated the need for continued treatment with Keppra.
Id. at 348.

Petitioner sent an email to Dr. Ramsay on October 3, 2016 about receiving the flu vaccine
in light of two “grand mal” seizures after the Tdap vaccine. Pet. Ex. 3 at 369. Dr. Ramsay’s office
advised her to get the flu vaccine. Id. at 372.

Petitioner returned to Dr. Ramsay on January 4, 2017 and reported a lot of anxiety and déjà
vu episodes in December of 2016 after she missed taking Keppra for several days, which stopped

8
when she restarted Keppra. Pet. Ex. 3 at 408. She was advised to take the Keppra as prescribed.
Id. at 416.

Petitioner presented to a new PCP on May 26, 2017 and reported that she was taking
Keppra for seizures but had not had any seizures in 2 years. Pet. Ex. 6 at 70. Her medical history
included arthritis, lipoma, seizures, and “[e]ncephalitis due to human herpes simplex virus
(HSV).” 10 Pet. Ex. 6 at 64.

It appears petitioner did not see Dr. Ramsay again until March 27, 2018, over a year after
her last visit. The record now included a diagnosis of “[p]artial symptomatic epilepsy with complex
partial seizures, not intractable, without status epilepticus.” Pet. Ex. 6 at 150. She reported monthly
episodes of “auras” and déjà vu feeling like something was going to happen. She does not lose
awareness during these episodes and can respond verbally. She was taking Keppra but was
concerned it causes depression. Id. at 153. She had no seizures since December 11, 2015. 11 Id. at
155. Dr. Ramsay documented no prior history of febrile seizure or family history of seizures. Id.
at 157. His impression remained “DPT reaction producing mild mesial temporal edema which has
improved”, insomnia, and “[p]rovoked seizure – the temporal relationship of the DPT shot and the
seizure and the MRI changes suggest the seizures was (sic) from a reaction to the DPT. Id. at 161.
He ordered eslicarbazepine (“Aptiom”) 800mg to start, which may increase to 1600mg depending
on blood level, and taper of Keppra to 500mg when Aptiom is started. Id.

Petitioner sent an email to Dr. Ramsay on March 30, 2018, stating that the addition of
800mg of Aptiom caused such extreme dizziness, nausea, and vertigo that she could not get out of
bed in the morning. Pet. Ex. 6 at 178. She was advised to decrease the Aptiom to 400mg and
continue with Keppra taper. Id. at 182. Petitioner responded a few days later that she felt fine with
400mg of Aptiom and 250mg of Keppra. Id.

A repeat MRI of the brain performed on April 2, 2018 revealed “subtle expansion with ill-
defined T2/FLAIR hyperintensity involving the cortex of the anteromedial aspect of the left
temporal lobe . . . concerning for focal cortical dysplasia or low-grade glioma.” The record
included that “[o]verall findings thought likely similar to that of prior studies, although better
delineated noting the use of a 3 Tesla magnet on today’s exam.” Pet. Ex. 6 at 197, 217. Aptiom
dosage was increased, and Keppra was discontinued. Id. at 225, 229.

In response to an email from petitioner, Dr. Ramsay’s office confirmed there were no
significant changes from her prior MRI studies. However, Dr. Ramsay was consulting with other
physicians and looking more closely at the study. Glioma 12 was not yet confirmed. Pet. Ex. 6 at
204.

10
Herpes encephalitis, and encephalitis in general, was ruled out by lumbar puncture which was negative for infection.
Pet. Ex. 3 at 157; Pet. Ex. 8 at 11-18.
11
Apart from her auras and déjà vu episodes, her last seizure was on December 8, 2015.
12
Glioma was initially understood to be a tumor composed of tissue representing neuroglia in any of its stages of
development but now is extended to include all the primary intrinsic neoplasms of the brain and spinal cord. Dorland’s
at 775.

9
Petitioner returned to Dr. Ramsay on April 9, 2018 and was advised that neuroradiology
review of the MRI confirmed cortical dysplasia as the most likely finding on the images. Pet. Ex.
6 at 217. She was to take 800mg of Aptiom and stop Keppra with levels tested in a week. Id. at
225. Petitioner sent an email to Dr. Ramsay to confirm that he no longer wanted her to see Dr. Bui,
who he referred her to for possible surgery for seizures. Id. at 237.

At her visit with Dr. Ramsay on July 11, 2019, she reported absence seizures while on
Aptiom. Pet. Ex. 39 at 33, 50, 80, 86.

The next day, she was transported to the hospital via ambulance and was actively seizing.
Pet. Ex. 43 at 84, 88. Her daughter reported convulsions with stiffness and foaming at the mouth.
Id. at 84. A history of seizures, encephalitis secondary to HSV, absence seizures once a month,
and a recent increased dosage of Aptiom causing illness were reported. Id. at 84, 89, 91, 93-94.
Lab work revealed low sodium (hyponatremia). Pet. Ex. 42 at 189. She was admitted to the ICU,
treated for hyponatremia, switched back to Keppra, and discharged on July 17, 2019. Id.; Pet. Ex.
43 at 98-99.

The following year, on July 16, 2020, petitioner presented to a new neurologist, Dr. Eady,
for “[e]pilepsy.” Pet. Ex. 29 at 57. Petitioner reported a history of a first seizure in December of
2015, first déjà vu event in 2012 during a walk for colon cancer, two febrile seizures at age 2, and
receipt of a pertussis vaccine with “?encephalitis.” Her son had a febrile seizure, otherwise there
was no family history. There was no head trauma, loss of consciousness, or central nervous system
infections. She reported about 75 episodes of déjà vu, 2 seizures in 2015, 1 in 2019, and 2 at 2
years of age. Id. at 58. She reported that she can have clusters of déjà vu episodes in a day then
none for a year but always at the same time during the month, with most triggered by stress, lack
of sleep, and possibly hormones. They occur mid-sentence where she is unable to respond but
remains aware. She has feelings of impending doom and déjà vu for 30 seconds, then she comes
“right back out of it.” Some episodes cluster with 3 in an hour. She reported being better using
biofeedback, pleasant thoughts, and breathing exercises. She was hospitalized 13 for seizures in
2015 after a pertussis shot and again in July of 2019 after increasing Aptiom with nausea and
hyponatremia. Id. Dr. Eady’s assessment was left temporal lobe epilepsy and essential tremor. Id.
at 60. Her brain MRI shows left amygdala enlargement – “FCD vs slow-growing neoplasm vs
sequela of encephalitis vs ictal sequela.” EEG shows left sharp waves. Dr. Eady referred her to
infectious disease 14 for “presumed encephalitis” after DPT. Id.

Petitioner presented to Dr. Eady a year later on June 17, 2021, reporting that she was
working in her garden with no seizure events. She had received all vaccinations except the
pneumococcal vaccine. Shingles made her arm hurt, she had no issues with the Pfizer COVID
vaccine, she was very active, watches her granddaughters, rides her bike for 7-10 miles, and had
no complaints. Pet. Ex. 29 at 9-10.

Only two visits with Dr. Eady were filed. No further records were filed.

13
Petitioner was treated in the ER and discharged.
14
The records show that petitioner attempted to make an appointment with an infectious disease physician but was
not able to get anything scheduled. Pet. Ex. 34 at 161; Pet. Ex. 35 at 46-50.

10
C. VAERS Reports

Multiple VAERS reports were filed. A typed VAERS report was completed by petitioner
on December 12, 2015 and included that she was “driving, getting off the interstate and evidently
had a seizure. I remember very little of the next 8 or so hours in the trauma center. I had no
warning.” Pet. Ex. 33 at 1.

A second typed report dated December 28, 2015 was completed by petitioner and included
a “Grand Mal Seizure while driving”, transport to a trauma center, “grand mal seizure again”, put
on Keppra, MRI, EEG abnormal, lumbar puncture, WBC normal. Pet. Ex. 33 at 3. Medical records
were attached. Id. at 4-26.

A handwritten VAERS report with a fax date of January 12, 2016 was competed by Edward
Mendez, pharmacy manager at Walgreens, and included Tdap vaccine given on December 5, 2015,
everything was fine, but 3 days later she had a seizure and was involved in an auto accident. She
went to the ER and had another seizure. She is under the care of a neurologist. Pet. Ex. 33 at 27.
Medical records were attached. Id. at 28-48.

A fourth VAERS report, handwritten by petitioner, was completed on December 18, 2015
and refers to Tdap and flu vaccines given within 30 days of each other. Pet. Ex. 33 at 49.

A fifth typed VAERS report was completed by Jorge Pesquera, dated May 17, 2016, and
included seizures, edema of the brain/temporal lobe swelling, and elevated CSF protein. Pet. Ex.
33 at 50. Attached is a typed “Event Description” that was “reported by a physician via call center
representative” of a 63-year-old female patient who received a “DTPa (Reduced antigen)
(Boostrix)” and five days later experienced a seizure. In December of 2015, petitioner experienced
brain edema, CSF increased protein, and was treated with Keppra. On an unknown date, the
outcome of the seizure, brain edema, and CSF protein increase was recovering/resolving. “It was
unknown if the reporter considered the seizure, brain edema and cerebrospinal fluid protein
increased to be related to Boostrix.” It was noted that petitioner had no past medical history of
seizures, had a seizure while driving which resulted in an accident, was taken to the ER and
admitted for an unknown amount of time, experienced brain edema of the temporal lobes seen on
MRI on December 24, 2015, and elevated protein on CSF. Other blood work was normal. Repeat
MRI on May 3, 2016 showed edema had resolved. Id. at 51.

A sixth VAERS report dated December 3, 2016 was completed by F. Khan and includes
“[a]ctivation of latent temporal lobe epilepsy…seizures…edema of the brain / Temporal lobe
swelling…motor vehicle accident.” The vaccination date is listed as December 3, 2015. Pet. Ex.
33 at 54. The “Event Description” contained on a separate page was reported by a physician to the
call center representative and included that petitioner received a Boostrix on December 3, 2015,
five days later experienced a seizure, presented to the ER, had brain edema and increased protein
in CSF in December of 2015, was treated with Keppra, and brain swelling and CSF levels were
recovering/resolving by an unknown date. “It was unknown if the reporter considered the seizure,
brain edema and cerebrospinal fluid protein increased to be” vaccine-related. The remainder of
that page was similar to the previous one filed but included follow up information received on
November 27, 2016, adding temporal lobe epilepsy, motor vehicle accident, and a medical history

11
that included “a single febrile seizure” and current condition of monthly “déjà vu episodes with
speech arrest.” The time from vaccine to onset of seizure changed from 5 days to 3 days. Also
added were lab results and that this was described in a case report as “activation of latent [temporal
lobe epilepsy]” with Boostrix. Id. at 55-57.

D. Petitioner’s Affidavits 15

Petitioner affirmed receipt of a Tdap vaccine on December 5, 2015 at Walgreens, then
“experienced grand mal seizures caused by the [Tdap] vaccination” and has suffered the “residual
effects or complications of the seizures” for more than six months. Pet. Ex. 5 at 1.

In a later affidavit, petitioner detailed one “déjà vu episode” in March of 2013 while on a
5-mile walk at a fundraising event. Pet. Ex. 25 at 1. She was “very aware” of her surroundings and
had an “overwhelming sense of dread.” She was under a lot of stress at the time. Id.

Petitioner reported the event to Dr. Short along with the stress she was under, but Dr. Short
felt no testing was necessary. 16 After that episode, she described being overwhelmed at times,
getting “a little fuzzy”, and having “to really focus on what was” before her, but she had no further
episodes like the one the day of the fundraiser. It did not affect her work, family, or home
environment. She did not have episodes in front of family or friends. Pet. Ex. 25 at 1.

Petitioner affirmed that she sold her house, “left [her] profession”, and moved in 2014.
Even though overwhelmed, there were no further episodes until “perhaps August of 2015” when
she “zoned out” at a yard sale while with her daughter. Pet. Ex. 25 at 1-2. This was the second
time she experienced déjà vu “where [she] felt overwhelming dread, was aware of [her]
surroundings, but the dread kept [her] from answering her question.” Id. at 2.

Petitioner affirmed she never had any prior adverse reactions to vaccinations and did not
recall any immediate reaction to the “DPT” vaccine on December 5, 2015, other than the usual
sore spot. Pet. Ex. 25 at 2.

Petitioner described the morning of December 8, 2015. It was a clear, cool day. While
driving, she encountered construction and traffic and got off at her exit which
“is the last thing [she] remember[s].” Pet. Ex. 25 at 2. She did not remember the accident, the
aftermath, or the birth of her granddaughter a week later. She recalled visiting a doctor, a referral
to and seeing a neurologist, having a brain scan on Christmas Eve, and being asked to return to the
hospital that day for a lumbar puncture due to the possibility of herpes encephalitis. Id.

Petitioner recalled seeing another neurologist over the next several months who ordered
multiple tests. She saw Dr. Ramsay in June of 2016 and asked when she could stop taking Keppra.

15
Petitioner filed a third affidavit on December 5, 2022, detailing a car accident in August of 2013. Pet. Ex. 45.
Petitioner’s affidavit appears consistent with the police report for that accident. Pet. Ex. 49. Petitioner filed
photographs of both cars involved. Pet. Ex. 46.
16
None of the records filed from Dr. Short’s office contained this information.

12
She was told the “lesions had diminished, [but] the encephalitis caused permanent changes on [her]
brain” and she needed medication for life. Pet. Ex. 25 at 3.

She recalled it was at this point, “or perhaps a little later,” that she became cognizant of
episodes of “absence seizures” at least once a month, with feelings of dread, not sleeping well the
night before, and having multiple episodes the next day sometimes with nausea beforehand and
being very tired afterward. She was never unaware of her surroundings. Pet. Ex. 25 at 3.

Petitioner told Dr. Ramsay about these episodes in 2017, but nothing was done until she
reported the episodes again in March of 2018. He changed her medication to Aptiom which
immediately made her ill with extreme nausea and dizziness. Pet. Ex. 25 at 3. After another MRI,
“all of a sudden” Dr. Ramsay said she had “focal cortical dysplasia.” He became “short” with her
when she asked why there was a new diagnosis not contained in prior MRIs and would not answer
her questions. 17 She then had “at least monthly episodes of what [she] was then told were absence
seizures in spite of the medication.” Id.

Petitioner took the Aptiom Dr. Ramsay prescribed but continued having absence seizures.
In May of 2019, she cut back on carbohydrates, which seemed to curb the absence seizures. 18 Pet.
Ex. 25 at 3.

Dr. Ramsay told her to keep a diary of the episodes. In July of 2019, she told him she had
seizures once a month and he told her to take 800mg of Aptiom in the morning and 800mg at night.
When she took the extra dose that evening, she became ill, unable to walk, and extremely nauseous.
She called Dr. Ramsay’s nurse and was advised to cut back on the medication. Pet. Ex. 25 at 3-4.
However, she developed absence seizures, had grand mal seizures, was transported to Ochsner
Hospital, and spent 5 days in the “Neuro ICU.” Aptiom was stopped, Keppra was restarted, and
she has been seizure-free since. She stopped seeing Dr. Ramsay in July of 2019 and now sees Dr.
Eady. Id. at 4.

E. Affidavit of Kate Uhle

Ms. Uhle is petitioner’s daughter. Pet. Ex. 26 at 1. She described a day in the fall of 2015
when she was having a conversation with petitioner at a yard sale and petitioner just stopped
responding. Petitioner nodded slightly when Ms. Uhle asked if petitioner had heard what she said.
Her eyes were moving around. Petitioner nodded slightly when Ms. Uhle asked if she was okay.
The episode lasted about a minute, then petitioner “just started talking again… explaining what
happened,” that she could hear Ms. Uhle and knew what was being said but could not respond.
Ms. Uhle never saw that happen before or at any point thereafter. Id.

Ms. Uhle was having her first child in December of 2015, and it was recommended that
petitioner receive the whooping cough vaccine since she was going to be the baby’s primary
caregiver when Ms. Uhle went back to work. Ms. Uhle did not remember the dates but believed
within 48 hours of petitioner’s receipt of the vaccine, she received a phone call from her husband

17
There appear to be no records that correspond with this conversation.
18
Id.

13
that petitioner had been involved in a car accident and was being taken to the hospital. Pet. Ex. 26
at 1. Upon Ms. Uhle’s arrival at the hospital, petitioner was on a stretcher in a neck brace, and
“very foggy and confused and kept asking [] what had happened and where she was.” She knew
her name and birthday but not who the president was or what they had named the baby. She
repeated the same questions, unable to retain any information from moments before. Id.

Ms. Uhle affirmed that petitioner had a seizure while in the ER with body convulsions and
foaming at the mouth. Afterward, she did not remember Ms. Uhle’s or Mr. Uhle’s names or her
address. Petitioner was sent home after she stabilized and underwent many tests. Pet. Ex. 26 at 2.

Ms. Uhle referred to the next several weeks as a “blur,” she had a newborn, and petitioner
was constantly confused with no recollection of the events over the past weeks. On Christmas Eve,
petitioner received a phone call to return to the ER because they thought she had “encephalitis on
her brain scan and warned her of the highly contagious nature of this.” Pet. Ex. 26 at 2. Everyone
was afraid for petitioner and because she had been around the newborn for two weeks. The brain
images confirmed “no significant sign of encephalitis.” Id.

Ms. Uhle described petitioner as confused with trouble remembering things throughout the
day following the car accident. She would repeat conversations, ask questions already answered,
and continually ask about the accident. Pet. Ex. 26 at 2. She started having absence seizures. Dr.
Ramsay prescribed medication and said these episodes were “normal and would continue to
happen.” Ms. Uhle recalled being at a visit to Dr. Ramsay when he mentioned “permanent changes
on the brain”, requiring medication for life. He also mentioned the possibility of a brain tumor
which he later dismissed. Id.

Ms. Uhle affirmed petitioner talked of frequent “episodes” over the years, not liking how
the medication made her feel, spotty memory, and episodes of sadness and depression. Pet. Ex. 26
at 2. She recalled that in July of 2019, Dr. Ramsay doubled petitioner’s medication to eliminate
the absence seizures but a “few days” later, petitioner did not feel well, threw up, was dizzy,
nauseous, tired, “puzzled” about why Ms. Uhle was there, and made no sense when Ms. Uhle
asked her questions. Id. Ms. Uhle’s husband called his brother who is an EMT and told them to
call 911. Id. at 3. Petitioner’s confusion continued, she did not recognize Mr. Uhle, then “she ‘came
to’” and started answering questions correctly. She explained to the EMTs how she felt, and they
recommended she go to the ER but could go by car. Id. While getting ready to go to the hospital,
Ms. Uhle found petitioner having a full body convulsion, groaning, and drooling in the bathroom.
She then became “stiff and rigid and shaking horribly.” Ms. Uhle “screamed for [her] husband to
call 911 again.” After a minute or so, she stopped seizing and stopped breathing, went completely
limp, then suddenly took a large gasp of air and started snoring as though sleeping deeply. Id. The
ambulance took her to the hospital. She was confused and could not form sentences or answer
questions. She had seizures in the ER with full body convulsions and foaming at the mouth. She
could not stay awake and when she was awake, she could not speak. She spent several days in the
ICU and had many tests. She was “hooked to a brain monitor that recorded activity as she would
have episodes.” Id.

According to Ms. Uhle, petitioner is no longer the person she was before the vaccine. She
was a teacher who remembered equations and scientific formulas. She now repeats herself and has

14
to be reminded of stories. Ms. Uhle worries “constantly. . . [that] she is unconscious in her home.”
Pet. Ex. 26 at 3-4.

IV. Expert and Treating Physician Opinions

A. Petitioner’s Expert, Dr. Nahm 19

Dr. Frederick Nahm 20 opined that the Tdap vaccination petitioner received caused
encephalitis, resulting in tonic/clonic generalized seizures, abnormalities of cerebral edema seen
on MRI, and focal left and right temporal slowing on EEG. Pet. Ex. 9 at 9. He discussed how anti-
NMDA receptors can produce an abnormal immune response to Tdap vaccination in some people,
trigger the loss of surface NMDA receptors, and lead to a defect in synaptic function and an
alteration in the balance between excitatory and inhibitory synaptic inputs. Id. at 6. Pertussis
vaccine specifically has been shown to result in overexpression of microRNA, which is associated
with anti-NMDA receptor encephalitis. Id.

According to Dr. Nahm, petitioner had no prior history of generalized seizures and this
new seizure within a reasonable degree of medical certainty was a response to the Tdap
vaccination. Pet. Ex. 9 at 7. Further, there was “irrefutable evidence” that petitioner had
encephalitis, with demonstrated neurological dysfunction in the form of generalized seizures,
confusion, and memory loss. Despite the lumbar puncture being “largely normal,” her CSF protein
was elevated, which is a marker for “encephalitides.” The initial elevation of her WBC could have
resolved by the time the LP was performed 16 days after the car accident. Id.; Pet. Ex. 17; 21 Pet.
Ex. 18. 22 Finally, edema on brain MRI is common in encephalitis. Pet. Ex. 9 at 7; Pet. Ex. 19.23
The improvement in edema on subsequent MRIs is consistent with an autoimmune or
inflammatory process and encephalitis. Pet. Ex. 9 at 8.

Further, Dr. Nahm argued that encephalitis could not be excluded because there was no
documented underlying malignancy or other abnormality that would explain her symptoms. Pet.
Ex. 9 at 8. He disagreed that petitioner had cortical dysplasia, which is a malformation deformity
present at birth and questioned how this developmental abnormality was not seen on initial MRIs.
Id.; Pet. Ex. 20 at 1, 3. He argued it was more likely that the vaccine led to temporal lobe
inflammation and “directly resulted” in the abnormality identified as cortical dysplasia, which was
only seen “well after the [Tdap] and the petitioner’s likely encephalitis.” Pet. Ex. 9 at 8; Pet. Ex.
20 at 2-3.

19
Petitioner first retained Dr. Nahm, who authored two reports filed in this matter. Pet. Ex. 9; Pet. Ex. 20. Petitioner
confirmed in a status report that she was not using Dr. Nahm’s opinion in support her Motion for Ruling on the Record.
ECF No. 80. Thus, Dr. Nahm’s reports are only briefly discussed because they are still part of the record.
20
Dr. Nahm is a practicing neurologist and is board certified in Psychiatry and Neurology. He holds an M.D. and a
Ph.D. Pet. Ex. 9 at 1.
21
V. Fominykh et al., Neuronal damage and neuroinflammation markers in patients with autoimmune encephalitis
and multiple sclerosis, 34 Metabolic Brain Disease 1473 (2019), filed as “Pet. Ex. 17.”
22
David N. Irani, Cerebrospinal Fluid in Clinical Practice (2008), filed as “Pet. Ex. 18.”
23
Michael E. Zapadka, Temporal Lobe Signal Abnormality, 4 J. Am. Osteopathic College of Radiology 22 (2015),
filed as “Pet. Ex. 19.”

15
Dr. Nahm argued that no evidence existed that was sufficient for a diagnosis of seizures
prior to vaccination. Pet. Ex. 9 at 7; Pet. Ex. 20 at 3-5. Déjà vu episodes are “common in the general
population” and petitioner did not have the distinct characteristics of déjà vu in temporal lobe
epilepsy which includes derealization, hallucinations, abdominal sensations, and fear. Pet. Ex. 9 at
7; Pet. Ex. 20 at 5. Further, petitioner only had a generalized tonic/clonic seizure post-vaccination,
“thus this is a new neurological condition that did not exist prior to the Tdap vaccination.” Pet. Ex.
9 at 7.

Dr. Nahm’s arguments and opinions are contrary to the medical records. Thus, even though
no longer relied upon by petitioner, they are still part of the record but are given little weight.

B. Petitioner’s Physician, Dr. Eady

Dr. Tiffany Eady 24 authored a letter dated February 3, 2022, writing that petitioner came
under her care in July of 2020 for focal epilepsy. Based on imaging, Dr. Eady favors cortical
dysplasia in the area of the left amygdala that has been stable for several years. Pet. Ex. 32 at 1.
She described this area of the brain as “extremely sensitive and has a high propensity to develop
seizures with any injury or inflammation.” Id. Dr. Eady included petitioner’s history of two febrile
seizures as a child which were self-limited and several episodes of focal onset “auras” that were
brief with preserved awareness and self-limited with no spread or secondary generalization and
did not require medication. Id.

According to Dr. Eady, petitioner received a Tdap vaccination and several days later had
several episodes of generalized convulsion with loss of awareness which resulted in a car accident
with injury and subsequent significant increase in aura frequency. Pet. Ex. 32 at 1. “The etiology
of the seizures was felt to be secondary to inflammation of the left mesial temporal structures
indicated by swelling (edema) in these structures as a direct reaction to the vaccine.” Id. Dr. Eady
submitted that encephalitis is an inflammation within the tissues of the brain, unlike meningitis
which is inflammation on the surface of the brain and it is possible to have encephalitis without
CSF changes. Id. Following these episodes, petitioner required treatment with anti-seizure
medications and had another convulsion in the setting of hyponatremia secondary to side effects
from one of the medications. “We will never know what her course would have been had she not
gotten the vaccination . . . considering the time course of events, is (sic) medically reasonable to
assume the vaccination was in part responsible for the focal brain inflammation and subsequent
seizures.” Id.

C. Petitioner’s Expert and Physician, Dr. Khan

Dr. Fawad Khan 25 is a neurologist. Dr. Khan routinely interprets EEG studies and
participated in petitioner’s treatment on May 9, 2016 following review of her chart and the 48-

24
Dr. Eady’s CV was not filed into the record. According to the Ochsner Health website
(https://blog.ochsner.org/biographies/tiffany-eady-md-phd/), Dr. Eady holds an M.D. and Ph.D. and is a subspecialist
in epileptology.
25
According to Dr. Khan, he is a full-time academic neurologist at Ochsner Health in New Orleans, Louisiana. He is
also an associate professor at Ochsner Clinical School and is board-certified in neurology, epilepsy, and clinical

16
hour EEG performed between May 4-6, 2016. Pet. Ex. 50 at 1. His report included what he learned
from her chart, more specifically that she was a 63-year-old woman with a prior history of a “single
febrile seizure” and self-described “intermittent episodes of déjà vu and staring spells for
approximately one year prior to the visit.” These clinical events were “highly suggestive of focal
seizures originating in the limbic cortical regions in the brain.” There was no reported loss of
consciousness or full body convulsions with these prior episodes. Id.

From petitioner’s chart, Dr. Khan learned that she had received a Tdap vaccination and
three days later lost consciousness while driving. Pet. Ex. 50 at 1. “She did report episodes
consistent with focal seizures 2 days prior to the seizure while driving.” She had no new
medications, alcohol, or drugs prior to the seizure while driving. She was taken to the hospital,
was alert with some disorientation while in the ER, then suffered another seizure with loss of
consciousness, foaming at the mouth, gurgling, urinary incontinence, followed by a post-ictal state
consistent with an electrographic seizure. After being stabilized, she was discharged home with
anti-seizure medication. Id.

Dr. Khan discussed the objective testing performed including, blood tests, brain MRI, EEG
studies, brain positron emission tomography (“PET”) scan, and cerebrospinal fluid analysis
(“CSF”). Pet. Ex. 50 at 2. He wrote that the December 24, 2015 brain MRI demonstrated abnormal
edema signal with slight fullness of the left mesial temporal lobe and insula lobe, with suggestion
of additional edema at right mesial temporal lobe and insula lobe, “highly suggestive of
encephalitis.” An MRI of the brain one month later revealed mild improvement of the abnormal
signals previously seen. An MRI of the brain three months later showed resolution of the abnormal
edema signals. The PET scan of the brain was unremarkable. The CSF testing performed on
December 24, 2015 was unremarkable but for “mildly increased protein at 45”, suggestive of
encephalitis. A paraneoplastic panel of the serum was non-revealing. Id.

Dr. Khan discussed the EEG findings. The first EEG done around December 24, 2015 at
the time of the first MRI showed abnormal left temporal slowing, a feature suggestive of temporal
lobe dysfunction. Pet. Ex. 50 at 2. The second EEG three weeks later was similar. The third EEG,
performed three months later when the third brain MRI showed resolution of the abnormal edema
signals, revealed independent left and right temporal focal polymorphic delta range slowing and
left temporal sharp waves. These findings were suggestive of dysfunction of both the left and right
temporal lobes and a focal epilepsy disorder. Id.

In a section of his report titled “Expert review”, Dr. Khan discussed submitting a case
report on petitioner to a national conference which was accepted for presentation by the American
Epilepsy Society 26 Annual Meeting on December 5, 2016, titled “Activation of Latent Temporal
Lobe Epilepsy After Tdap Vaccine (Boostrix®) – MRI and EEG Correlates.” 27 A copy of the
abstract was filed. Pet. Ex. 50 at 2-3. The abstract includes only the “Results” that the patient

neurophysiology. He has practiced since 2012 and serves as the section head of the epilepsy division of Ochsner
Neurosciences Institute. Pet. Ex. 50 at 1.
26
In response to a subpoena, the American Epilepsy Society stated that it had no responsive documents, that only the
abstract of the study was published, and provided a link. Pet. Ex. 44. The full study was never filed in this case.
27
The case study was authored by Dr. Khan, Dr. Ramsay, and Jorge Pesquera (who submitted one of the various
VAERS reports filed). See Pet. Ex. 33 at 50.

17
remained seizure free as of November 22, 2016 (when published) while on Keppra. Pet. Ex. 44 at
2. It also notes that the CSF showed mildly elevated protein, and paraneoplastic panel was
negative; an initial MRI revealed abnormal fluid-attenuated inversion recovery (FLAIR) signal
hyperintensity within the bilateral insula and mesial temporal lobes without enhancement, left
worse than right with resolution of the abnormalities by the third MRI study; PET scan of the brain
was unremarkable; initial EEG revealed focal slowing in the left temporal region; repeat EEGs
revealed independent left and right temporal focal slowing as well as left temporal sharp waves.
Id. The “Conclusions” included that seizures were not reported in clinical trials for the Boostrix
vaccine, however post-marketing surveillance included several neurological complications
including questionable GBS, Bell’s palsy, seizure, demyelinating diseases, and
encephalopathy/encephalitis. Some of these patients had a history of anti-convulsive treatment,
EEG abnormalities, and seizures before vaccination. Id. The subject of this case study (petitioner)
had a “clinical history preceding the seizure along with EEG findings [that] supports a diagnosis
of temporal lobe epilepsy (TLE). Although it is possible that the seizures following the vaccination
was only a coincidental temporal association, the development of focal encephalitis and clinical
seizures shortly after the vaccination and improvement in the MRI signal abnormality over time
are highly suggestive of a direct consequence of the vaccination. This phenomenon would support
the theory that TLE may have an underlying neuro-inflammatory pathogenesis.” Id. at 2-3.

Dr. Khan provided the ingredients of the Boostrix vaccine (Tdap) which includes tetanus
toxoid, diphtheria toxoid, and inactivated pertussis antigens, as well as formaldehyde-treated
filamentous hemagglutinin and pertactin, aluminum hydroxide, sodium chloride, residual
formaldehyde, and polysorbate 80. He noted that a clinical trial prior to approval was significant
only for headache post-vaccination. 28 Pet. Ex. 50 at 2.

Dr. Khan cited Chang and Sun in support of his opinion that the Boostrix vaccine can cause
seizures. He wrote that Chang observed post-marketing surveillance of the Boostrix vaccine a total
of 28 cases with seizures after vaccination with Tdap and other concomitant vaccines including
meningococcal, Hep A, Hep B, Varicella, and MMR, and 9 cases after Tdap alone. The median
age was 15 with a range between 9 and 38 years of age. Six of the 28 cases had a prior history of
anti-convulsive treatment or EEG abnormalities prior to vaccination, while seven of the 28 cases
had a history of seizures including 2 who had seizures following prior vaccination. Pet. Ex. 50 at
3; Pet. Ex. 51. 29 Sun was a population-based study of children in Denmark who received the
combined diphtheria-tetanus toxoids-acellular pertussis-inactivated poliovirus-Haemophilus
influenzae type b (DTaP-IPV-Hib) vaccination and showed a small increased risk of “febrile
seizures” on the day of the first two vaccinations at 3 and 5 months of age. “Vaccination, however,
was not associated with an increased risk of epilepsy.” Pet. Ex. 50 at 3; Pet. Ex. 52. 30

Dr. Khan opined that petitioner suffered encephalitis from the Tdap vaccination. He
described encephalitis as the result of a “complex neuro-inflammatory process” and relied on
Herve to show that vaccinations lead to a “complex cascade of immunological activations,” which

28
The reference was to a link.
29
Soju Chang et al., U.S. Postlicensure safety surveillance for adolescent and adult tetanus, diphtheria and acellular
pertussis vaccines: 2005–2007, 31 Vaccine 1447 (2013), filed as “Pet. Ex. 51.”
30
Yuelian Sun et al., Risk of Febrile Seizures and Epilepsy After Vaccination With Diphtheria, Tetanus, Acellular
Pertussis, Inactivated Poliovirus, and Haemophilus Influenzae Type b, 307 JAMA 823 (2012), filed as “Pet. Ex. 52.”

18
includes strong expression of proinflammatory cytokines, the activation of complement, and
cellular recruitment. Pet. Ex. 50 at 3-4; Pet. Ex. 53. 31 He referenced Vezzani to show that these
inflammatory mediators have been detected in epilepsy brain specimens, have been associated
with the promotion of local inflammation, and are thought to function as “’neuromodulators’”
directly affecting neuronal function and excitability leading to seizures. Pet. Ex. 50 at 4; Pet. Ex.
55. 32 He relied on Baldelli to show that in some predisposed people, an excessive innate immune
response to a vaccine may lead to a “cytokine storm”, which in turn can lead to brain inflammation
then dysfunction. Pet. Ex. 50 at 4; Pet. Ex. 54. 33 Further, he relied on van Vliet to show that during
focal inflammation, there is a disruption of the blood brain barrier, resulting in exposure of the
brain to these mediators and thereby increasing the risk of seizures and epilepsy progression. Pet.
Ex. 50 at 4; Pet. Ex. 56. 34 Dr. Khan then provided a list of articles—including Gershman, Fan,
Casey, Bitnun, Rogalewski, Kaplanski, Pirmohamed, Sriram, and Gamboa—to show that his
hypothesis is supported by other vaccinations that can cause encephalitis, including vaccines for
yellow fever, COVID 19, smallpox, measles, hep A, hep B, poliovirus, pertussis (whole cell), and
rabies. Pet. Ex. 50 at 4-5; Pet. Ex. 57; 35 Pet. Ex. 58; 36 Pet. Ex. 59; 37 Pet. Ex. 60; 38 Pet. Ex. 61;39
Pet. Ex. 62; 40 Pet. Ex. 63; 41 Pet. Ex. 64; 42 Pet. Ex. 65. 43

Dr. Khan concluded that based on the foregoing and his clinical judgment, petitioner
suffered a “transient syndrome of encephalitis following the Tdap vaccination and that this
temporal association is based on causation.” Pet. Ex. 50 at 3. Further, “[t]he encephalitis manifest
(sic) in activation and revving up the disease processes of her epilepsy resulting in a generalized
seizure while driving. The close proximity of the events to the vaccination and the objective
findings on brain imaging (with broad involvement of multiple lobes) and cerebrospinal fluid

31
Caroline Hervé et al., The how’s and what’s of vaccine reactogenicity, 4 npj Vaccines (2019),
https://doi.org/10.1038/s41541-019-0132-6, filed as “Pet. Ex. 53.”
32
Annamaria Vezzani et al., IL-1 receptor/Toll-like receptor signaling in infection, inflammation, stress and
neurodegeneration couples hyperexcitability and seizures, 25 Brain, Behavior, and Immunity 1281 (2011), filed as
“Pet. Ex. 55.”
33
Luca Baldelli et al., Hyperacute reversible encephalopathy related to cytokine storm following COVID-19 vaccine,
358 J. Neuroimmunology 577661 (2021), filed as “Pet. Ex. 54.”
34
E. A. van Vliet et al., Blood–brain barrier leakage may lead to progression of temporal lobe epilepsy, 130 Brain
521 (2007), filed as “Pet. Ex. 56.”
35
Bruno Fukelmann Guedes et al., Potential autoimmune encephalitis following yellow fever vaccination: A report of
three cases, 355 J. Neuroimmunology 577548 (2021), filed as “Pet. Ex. 57.”
36
H.-T. Fan et al., COVID-19 vaccine-induced encephalitis and status epilepticus, QJM: Int’l J. of Med. (2022),
https://doi.org/10.1093/qjmed/hcab335, filed as “Pet. Ex. 58.”
37
Christine Casey et al., Surveillance Guidelines for Smallpox Vaccine (vaccinia) Adverse Reactions, 55 MMWR 1
(2006), filed as “Pet. Ex. 59.”
38
Cristina Costales et al., Vaccine-Associated Measles Encephalitis in Immunocompromised Child, California, USA,
28 Emerging Infectious Diseases 906 (2022), filed as “Pet. Ex. 60.”
39
Andreas Rogalewski et al., Improvement of advanced postvaccinal demyelinating encephalitis due to
plasmapheresis, 3 Neuropsychiatric Disease and Treatment 987 (2007), filed as “Pet. Ex. 61.”
40
Shaw FE et al., Central nervous system demyelination after vaccination against hepatitis B and HLA haplotype, 58
J. Neurology, Neurosurgery, and Psychiatry 758 (1995), filed as “Pet. Ex. 62.”
41
Munir Pirmohamed & Peter Winstanley, Hepatitis B vaccine and neurotoxicity, 73 Postgrad Med. J. 462 (1997),
filed as “Pet. Ex. 63.”
42
S. Sriram, M.D. & L. Steinman, M.D., Postinfectious and Postvaccinial Encephalomyelitis, 2 Neurologic Clinics
341 (1984), filed as “Pet. Ex. 64.”
43
E. T. Gamboa, MD et al., Delayed Onset of Post-Rabies Vaccination Encephalitis, 13 Annals of Neurology 676
(1983), filed as “Pet. Ex. 65.”

19
analysis corroborate this medical postulation. No other explanation was determined, and no other
etiologies could be accounted for this observation.” Id.

Dr. Khan then responded to what he expected would be the counterarguments to his
opinion—that temporal relationship does not equate to causation that “the seizure was a result of
a non-specific activation of latent epilepsy”, and that the test results and findings on imaging were
due to an unknown acute encephalitis—writing, “this type of clinical phenomenon . . . is clinically
considered to be extremely unlikely.” Pet. Ex. 50 at 5.

Dr. Khan did not address petitioner’s cortical dysplasia. See generally Pet. Ex. 50.

D. Respondent’s Expert, Dr. Evans

Dr. Steven Evans 44 opined that petitioner has focal epilepsy due to cortical dysplasia
unrelated to the Tdap vaccination. Resp. Ex. A at 10; Resp. Ex. C at 1, 5. He detailed petitioner’s
medical history which included a febrile convulsion at age 2, the concern in October of 2015 for
sleep apnea and chronic myoclonus, affirmed experiences of déjà vu episodes since 2013
associated with stress and feelings of dread, a seizure and car accident on December 8, 2015, her
medical course thereafter, and the diagnosis of cortical dysplasia. Resp. Ex. A at 1-6; Resp. Ex. D
at 1, 2. Dr. Evans included that febrile seizures are a risk factor for later development of temporal
lobe epilepsy. Resp. Ex. D at 3; Resp. Ex. D Tab 1; 45 Resp. Ex. D Tab 2; 46 Resp. Ex. D Tab 3. 47

Dr. Evans explained that the April 2, 2018 MRI performed years after seizure onset and
well after any acute MRI changes caused by the December 8, 2015 seizure should have resolved,
used seizure protocol designed to show subtle lesions in the temporal lobe. It was interpreted as
most likely showing cortical dysplasia and less likely low-grade glioma, both of which are
common causes of temporal lobe epilepsy. Resp. Ex. C at 3.

Dr. Evans described petitioner’s déjà vu episodes as focal seizures, explaining that déjà vu
is a common seizure symptom in temporal lobe epilepsy. Resp. Ex. A at 6; Resp. Ex. C at 2; Resp.
Ex. D at 3. Complex partial seizures are associated with amnesia in temporal lobe epilepsy, and
unresponsive staring is a common symptom of complex partial seizures. Resp. Ex. A at 7; Resp.
Ex. D at 3. He opined that the seizure petitioner had at the hospital after the car accident was likely
a complex partial seizure because she seemed to retain capacity for semi-purposeful behavior and
had amnesia after. Resp. Ex. A at 7. Dr. Evans further noted that it is not unusual for patients to
have subtle focal seizures for some time before suffering from a generalized or complex partial
seizure and then seeking care. Id. at 9; Resp. Ex. C at 1.

44
Dr. Evans is a practicing general neurologist with subspecialty in the diagnosis and treatment of epilepsy. Resp. Ex.
A at 1. He is board-certified in neurology and in clinical neurophysiology and epilepsy. He served as the Director of
the Epilepsy Division at University of Louisville Hospital, where he is currently a full professor in the neurology
department. Id.; Resp. Ex. B.
45
Michael Duchowny, Febrile Seizures, in The Treatment of Epilepsy: Principles and Practice (Elaine Wyllie ed.,
2001), filed as “Resp. Ex. D Tab 1.”
46
Katelin P. Patterson et al., Origins of Temporal Lobe Epilepsy: Febrile Seizures and Febrile Status Epilepticus, 11
Neurotherapeutics 242 (2014), filed as “Resp. Ex. D Tab 2.”
47
Aakriti Tiwari et al., Febrile Seizures in Children: A Review, 14 Cureus e31509 (2022), filed as “Resp. Ex. D Tab
3.”

20
Dr. Evans defined epilepsy as any condition that causes recurrent unprovoked seizures and
is often caused by lesions on the brain, such as cortical dysplasia. Resp. Ex. A at 7. Cerebral
cortical dysplasia is a brain developmental abnormality present at birth and is a common cause of
epilepsy later in life. Id.; Resp. Ex. A Tab 16. 48 Petitioner’s epilepsy was due to cortical dysplasia
with onset at least a year prior to vaccination evidenced by her déjà vu episodes. Resp. Ex. A at 7,
10; Resp. Ex. C at 1-2, 5; Resp. Ex. D at 3, 5.

Dr. Evans agreed with the radiological interpretation of petitioner’s first MRI that “the
evidence is strongly in favor” of the abnormalities/edema being caused by the seizure, which is
consistent with the later MRIs that showed improvement then resolution without any treatment
and without further symptoms. Resp. Ex. A at 8; Resp. Ex. C at 4-5; Resp. Ex. D at 3, 4, 7. He
referred to Kim, which showed that the MRI appearance of limbic encephalitis and edema from
recent seizures look very similar. Resp. Ex. D at 7; Resp. Ex. C Tab 2; 49 Pet. Ex. 61. 50 He noted
Dr. Ramsay’s opinion that petitioner had temporal lobe edema and a “provoked seizure due to
DPT injection,” asserting that petitioner has epilepsy, not a provoked seizure, otherwise she would
not have had continued simple partial seizures, and Dr. Ramsay would not have had to continue
treating, testing, and medicating petitioner. Resp. Ex. A at 8, 10; Resp. Ex. C at 1, 5; Resp. Ex. D
at 2.

Further, Dr. Evans disagreed that petitioner had encephalitis, pointing out that all testing
was negative. He acknowledged that encephalitis can cause seizures, but encephalitis when present
also causes fever, cognitive dysfunction or coma, severe headache, and sometimes focal
neurological deficits, none of which petitioner presented with or complained of. Resp. Ex. A at 8;
Resp. Ex. C at 4-5; Resp. Ex. D at 5-6; Pet. Ex. 57; 51 Pet. Ex. 58. 52 Further, Dr. Nahm suggested
that petitioner had NMDA receptor antibody-mediated encephalitis, which presents with
psychiatric abnormality, encephalopathy, and recurrent seizures. Resp. Ex. A at 8-9. Petitioner did
not have any of those symptoms, testing was negative with no support for a diagnosis of NMDA
receptor antibody-mediated encephalitis. Id. at 9. Petitioner’s symptoms on December 8 were not
concerning for encephalitis, which is why she was discharged from the hospital. Resp. Ex. D at 6.

Dr. Evans explained that temporal lobe abnormalities like the ones seen on the first MRI
and new-onset seizures can suggest encephalitis, which is why the lumbar puncture was performed
to rule it out. Resp. Ex. A at 8; Resp. Ex. D at 6-7. The CSF in encephalitis shows signs of
inflammation including elevated white blood cell count, elevated protein, and sometimes elevated
red blood cell count. Resp. Ex. D at 6; Pet. Ex. 57; 53 Pet. Ex. 58; 54 Pet. Ex. 61; 55 Pet. Ex. 65.56
Petitioner’s lumbar puncture results were normal with normal white and red blood cell count,

48
Siegel et al., supra note 7.
49
Si Eun Kim et al., Characteristics of seizure-induced signal changes on MRI in patients with first seizures, 48
Seizure 62 (2017), filed as “Resp. Ex. C Tab 2.”
50
Rogalewski et al., supra note 39.
51
Guedes et al., supra note 35.
52
Fan et al., supra note 36.
53
Guedes et al., supra note 35.
54
Fan et al., supra note 36.
55
Rogalewski et al., supra note 39.
56
Gamboa et al., supra note 43.

21
which “strongly mitigates against encephalitis.” Resp. Ex. A at 8. Dr. Evans added that “it is well
known that CSF protein goes up with age” and petitioner’s protein was only mildly elevated at 45.
Id. at 9; Resp. Ex. D at 6. Citing Breiner, Dr. Evans explained that he was taught to allow 1 mg/dl
per year of age, which for petitioner at the time of vaccination would have meant a normal protein
level was 63; her protein level was 45. Id.; Resp. Ex. A Tab 5. 57 Petitioner’s treating physicians
“obviously did not consider her LP results or her symptoms to be concerning for encephalitis”
because they discharged her home. Resp. Ex. D at 6. The only evidence suggesting encephalitis
was the abnormal MRI on December 24, which is better explained by cortical dysplasia and
residuals from the seizures. Resp. Ex. A at 9.

Dr. Evans “strongly disagree[d]” with Dr. Eady’s and Dr. Khan’s opinions that the Tdap
vaccination caused encephalitis which exacerbated her epilepsy. He was confused by Dr. Eady’s
opinion and whether she believed the vaccination caused only the December 8, 2015 seizure or
contributed in some larger way to petitioner’s epilepsy. Regardless, there was no evidence that
petitioner had brain inflammation and no evidence that the vaccination played any role in her
seizures. He noted that Dr. Eady and Dr. Khan agreed that petitioner was having focal seizures
prior to the Tdap vaccination, and focal seizures indicate the presence of epilepsy; thus, petitioner’s
epilepsy began prior to her receipt of the vaccine. Resp. Ex. D at 4-5. Further, “generalized seizures
usually do eventually occur in patients with focal epilepsy.” Id. at 5. Thus, the December 8, 2015
seizure was due to petitioner’s pre-existing epilepsy—not the vaccination. Id. at 5, 6.

Moreover, studies have failed to show any association between vaccination and poor
neurological outcomes. Resp. Ex. A at 9; Resp. Ex. A Tab 6. 58 Dr. Evans acknowledged that the
package insert for the Tdap vaccine lists encephalopathy within 7 days of administration of a
previous dose of a pertussis-antigen vaccine not attributable to another cause as a contraindication
of future pertussis-antigen vaccines. Resp. Ex. A at 9; Resp. Ex. A Tab 2. 59 However, acellular
pertussis vaccines are now standard in the U.S. and other developed countries. The rates of adverse
events with acellular pertussis were reduced by 2/3 once the switch was made from whole cell
pertussis vaccines. Resp. Ex. A at 9; Resp. Ex. A Tab 8; 60 Resp. Ex. A Tab 15. 61

As a clinician, Dr. Evans recommends that his patients receive all recommended vaccines.
He also recommends an antipyretic if they develop a fever after getting a vaccine, which is very
common, because fever may lower seizure threshold. Resp. Ex. A at 9-10. Nevertheless, there is
no evidence that a post-vaccination fever is any more likely to produce seizures than a fever for
any other reason. Id. at 10. Haberg, Barlow, and Vestergaard all support that vaccination or febrile

57
Ari Breiner et al., Adult CSF total protein upper reference limits should be age-partitioned and significantly higher
than 0.45 g/L: a systematic review, 266 J. Neurology 616 (2019), filed as “Resp. Ex. A Tab 5.”
58
Natasha J. Brown et al., Vaccination, seizures and ‘vaccine damage’, 20 Current Opinion in Neurology 181 (2007),
filed as “Resp. Ex. A Tab 6.”
59
BOOSTRIX Prescribing Information, (2019), filed as “Resp. Ex. A Tab 2.”
60
Centers for Disease Control, Surveillance Summaries, 52 MMWR SS-1 (2003), filed as “Resp. Ex. A Tab 8.”
61
Steven Rosenthal et al., The Safety of Acellular Pertussis Vaccine vs Whole-Cell Pertussis Vaccine, 150 Archives
of Pediatric & Adolescent Med. 457 (1996), filed as “Resp. Ex. A Tab 15.”

22
seizures after vaccination are not associated with an increased risk of epilepsy. Resp. Ex. A at 10;
Resp. Ex. A Tab 3; 62 Resp. Ex. A Tab 12; 63 Resp. Ex. A Tab 17. 64

Summarily, Dr. Evans opined that petitioner had focal epilepsy before she received the
subject Tdap vaccine on December 5, 2015, then had her first generalized seizure due to her
epilepsy three days post-vaccination, her epilepsy was caused by cortical dysplasia not the Tdap
vaccination, and petitioner never had encephalitis. Resp. Ex. D at 7.

V. The Parties’ Arguments

A. Petitioner’s Motion for Ruling on the Record

Petitioner argued that she is entitled to compensation for the Table injury of encephalitis
caused by the Tdap vaccine she received on December 5, 2015. Motion at 1. She detailed the Table
criteria for encephalitis, submitting that she had neurologic dysfunction in the form of generalized
seizures, confusion, and memory loss on December 8, 2015 and the elevated protein in the CSF
was evidence of an inflammatory process in the brain. Id. at 9-10. Additionally, the MRI findings
of edema and abnormal EEG findings were consistent with encephalitis. Id. at 10-11. The onset of
her encephalitis was within 72 hours after receiving the Tdap vaccine, and the sequelae of her
encephalitis lasted beyond six months. Id. at 11-13. Finally, petitioner submitted that she met none
of the exclusionary criteria for a Table encephalitis. Id. at 13.

Petitioner claimed that the encephalitis caused by the Tdap vaccine activated her temporal
lobe epilepsy. Motion at 13. She acknowledged the diagnosis of cortical dysplasia but argued that
not all cortical dysplasia malformations are epileptic. Id. She relied on Najm, which was not filed
as an exhibit in this case but attached for the first time to petitioner’s Motion, to show that some
patients with cortical dysplasia do not develop epilepsy until later in life, and when they do it is
after a trigger like trauma, infection, stress, or sleep deprivation. Id. at 14, 18-29. Petitioner
referenced Kasper and Fauser, also not filed during the pendency of this case but attached to her
Motion, to show that there is evidence that the onset of epilepsy can occur at any point over the
span of decades in patients with cortical dysplasia. Id. at 14, 30-46.

Petitioner further argued that Vezzani shows that “pro-epileptic injuries” activate
inflammatory pathways that can cause recurrent seizures and that experiments show that CNS
inflammation can change brain excitability and increase the likelihood of future seizures. Motion
at 14; Pet. Ex. 55. 65 Together, this supports that “inflammatory processes are induced in the brain
following infection, … febrile seizures, status epilepticus, which are all events associated with the
occurrence of symptomatic seizures with an increased risk of developing epilepsy.” Motion at 14-
15; Pet. Ex. 55.

62
William E. Barlow et al., The Risk of Seizures After Receipt of Whole-Cell Pertussis or Measles, Mumps, Rubella
Vaccine, 345 New Eng. J Med. 656 (2001), filed as “Resp. Ex. A Tab 3.”
63
Siri E. Haberg et al., Epilepsy in Children After Pandemic Influenza Vaccination, 141 Pediatrics e20170752 (2018),
filed as “Resp. Ex. A Tab 12.”
64
Mogens Vestergaard et al., MMR Vaccination and Febrile Seizures: Evaluation of Susceptible Subgroups and Long-
term Prognosis, 292 JAMA 351 (2004), filed as “Resp. Ex. A Tab 17.”
65
Vezzani et al., supra note 32.

23
Petitioner submitted that in Dr. Eady’s opinion, the etiology of petitioner’s seizures was
the brain inflammation caused by the Tdap vaccination and that petitioner has cortical dysplasia.
Motion at 15.

Finally, petitioner noted that three other cases in the Vaccine Program involved an
underlying cortical dysplasia. In Heilig v. Sec’y of Health & Human Servs., Dr. Kinsbourne
theorized that the DTaP vaccine was a “second hit” that triggered epilepsy in a child with a “very
small abnormality” in the frontal lobe and that second hit “was needed before [the child’s] first
seizure occurred.” The special master found that preponderant evidence supported the DTaP
vaccine caused the child to develop epilepsy. No. 16-140V, 2024 WL 929030 (Fed. Cl. Spec. Mstr.
Feb. 7, 2024); Motion at 15. In Reilly v. Sec’y of Health and Human Servs., the special master
determined that the pertussis component of the DTaP vaccine acted as a “second hit”, causing the
onset of infantile spasms in the context of a focal cortical dysplasia. No. 09-489V, 2016 WL
3456844, at *13-15 (Fed. Cl. Spec. Mstr., May 31, 2016); Motion at 15-16. However, in Akers v.
Sec’y of Health and Human Servs., the special master did not find the theory—cytokines produced
in response to vaccination crossed the blood-brain-barrier and overactivated the already
susceptible cortical dysplasia—to be persuasive. No. 15-597V, 2021 WL 3560069 (Fed. Cl. Spec.
Mstr. July 6, 2021); Motion at 16.

Petitioner concluded that when “[a]pplying the ‘second hit’ theory to the facts of the instant
case, there is preponderant evidence to establish that the [Tdap] vaccination served as the ‘second
hit’ causing Petitioner to develop focal epilepsy.” Motion at 16. She acknowledged staring spells
that predated the vaccination but stated that her first grand mal seizure only occurred after the
vaccine; but for the vaccine, petitioner would not have developed focal epilepsy. Id.

Petitioner’s Motion for Ruling on the Record was the first time she mentioned a two-hit
theory, which was not addressed by any of her treating doctors or experts.

B. Respondent’s Response

Respondent argued that petitioner failed to satisfy the Table requirements for an
encephalitis following Tdap vaccination. Further, petitioner failed to meet any of the three Althen
prongs required to prove causation-in-fact. Response at 1-2. Rather, petitioner’s epilepsy predated
and was thus unrelated to the Tdap vaccine she received on December 5, 2015. Id. at 4.

Respondent argued that petitioner’s evidence does not support a diagnosis of encephalitis
and that petitioner “appears to maintain a related causation-in-fact claim”, alleging that a Table
encephalitis activated her temporal lobe epilepsy. However, petitioner failed to prove any off-
Table injury. Response at 12-13.

Regarding the Table encephalitis, petitioner’s symptoms, including déjà vu episodes and
myoclonic jerking during sleep, began at least two years prior to vaccination. Response at 18, 20.
Petitioner had no central nervous system findings, and no inflammatory process was seen on CSF
testing. Id. at 18-19. Other than the abnormal MRI finding, no evidence was consistent with
encephalitis. Id. at 19. Dr. Evans agreed with the interpretation of the radiologist reading

24
petitioner’s MRI films that the initial MRI findings can be better explained as resulting from
cortical dysplasia and seizure activity than encephalitis. Id. at 19-21; Resp. Ex. A Tab 16. 66

Further, petitioner failed to provide a sound and reliable theory to satisfy Althen Prong 1,
instead simply submitting that petitioner suffered an encephalitis from the Tdap vaccination, which
caused her epilepsy. Response at 22. Dr. Evans acknowledged the increased risk of seizure with
fever. Id. Petitioner did not allege nor would the records support that she suffered any fever
between December 5 and December 8, 2015. Regardless, febrile seizures are not associated with
increased risk of epilepsy. Id. at 23; Resp. Ex. A Tab 3; 67 Resp. Ex. A Tab 17. 68 Petitioner’s experts
also failed to provide any opinion connecting the genetic bases of epilepsy and the role of
environmental triggers. Response at 24.

Respondent acknowledged that the opinions of treating physicians are generally afforded
weight. Response at 25-27. However, while Drs. Eady and Khan treated petitioner at some point
post-vaccination, neither treated her during her initial presentation and both relied on the presence
of encephalitis to explain petitioner’s seizure disorder. However, petitioner was not diagnosed with
or treated for encephalitis. Id. at 26-27.

Respondent concluded that petitioner suffered from focal epilepsy due to cortical dysplasia
prior to her receipt of the Tdap vaccine and suffered a generalized seizure coincidently three days
after the vaccination. Response at 21, 27-28. Although encephalitis was considered, it was
investigated and ruled out by testing. Id. at 21. There is no scientific evidence that supports Tdap
vaccine causing focal epilepsy in the context of cortical dysplasia. Id. at 24; Akers, No. 15-597V,
2021 WL 3560069, at *39 (“FCD [focal cortical dysplasia] is highly correlated with epilepsy
without need for a trigger”).

VI. Legal Standards

A. Table Injury

The Vaccine Act provides two avenues for petitioners to receive compensation. First, a
petitioner may demonstrate a “Table” injury—i.e., an injury listed on the Vaccine Injury Table
that occurred within the provided time period. § 11(c)(1)(C)(i). “In such a case, causation is
presumed.” Capizzano v. Sec’y of Health & Human Servs., 440 F.3d 1317, 1320 (Fed. Cir. 2006);
see § 13(a)(1)(B).

A vaccine recipient shall be considered to have suffered an on-Table encephalitis if any
injury meeting the description below of acute encephalitis occurs within 72 hours following
vaccination and results in a chronic encephalopathy,

(i) Acute encephalitis. Encephalitis is indicated by evidence of neurologic
dysfunction, as described in paragraph (c)(3)(i)(A) of this section, plus evidence of

66
Siegel et al., supra note 7.
67
Barlow et al., supra note 62.
68
Vestergaard et al., supra note 64.

25
an inflammatory process in the brain, as described in paragraph (c)(3)(i)(B) of this
section.

(A) Evidence of neurologic dysfunction consists of either:

(1) One of the following neurologic findings referable to the CNS: Focal cortical
signs (such as aphasia, alexia, agraphia, cortical blindness); cranial nerve
abnormalities; visual field defects; abnormal presence of primitive reflexes (such
as Babinski’s sign or sucking reflex); or cerebellar dysfunction (such as ataxia,
dysmetria, or nystagmus); or

(2) An acute encephalopathy as set forth in paragraph §100.3(c)(2)(i) of this
section.

(B) Evidence of an inflammatory process in the brain (central nervous system or
CNS inflammation) must include cerebrospinal fluid (CSF) pleocytosis (>5 white
blood cells (WBC)/mm in children > 2 months of age and adults; > 15 WBC/mm
in children <2 months of age); or at least two of the following:

(1) Fever (temperature > 100.4 degrees Fahrenheit);

(2) Electroencephalogram findings consistent with encephalitis such as diffuse or
multifocal nonspecific background slowing and periodic discharges; or

(3) Neuroimaging findings consistent with encephalitis, which include, but are not
limited to brain/spine magnetic resonance imaging (MRI) displaying diffuse or
multifocal areas of hyperintense signal on T2-weighted, diffusion-weighted image,
or fluid-attenuation inversion recovery sequences.

42 C.F.R. §100.3(c)(3).

The exclusionary criteria for encephalitis include an underlying malignancy that led to a
paraneoplastic encephalitis; an infectious disease associated with encephalitis; acute disseminated
encephalomyelitis (“ADEM”); or other conditions or abnormalities that would explain the vaccine
recipient's symptoms. 42 C.F.R. §100.3(c)(3)(ii).

B. Off-Table Injury

The second avenue for petitioners to receive compensation, where the alleged injury is not
listed on the Vaccine Injury Table, is an “off-Table” injury, which requires that the petitioner
“prove by a preponderance of the evidence that the vaccine at issue caused the injury.” Capizzano,
440 F.3d at 1320; see § 11(c)(1)(C)(ii). Initially, a petitioner must provide evidence that he or she
suffered, or continues to suffer, from a definitive injury. Broekelschen v. Sec’y of Health & Human
Servs., 618 F.3d 1339, 1346 (Fed. Cir. 2010); Lombardi v. Sec’y of Health & Human Servs., 656
F.3d 1343, 1353 (Fed. Cir. 2011). A petitioner need not show that the vaccination was the sole
cause, or even the predominant cause, of the alleged injury; showing that the vaccination was a

26
“substantial factor” and a “but for” cause of the injury is sufficient for recovery. See Pafford v.
Sec’y of Health & Human Servs., 451 F.3d 1352, 1355 (Fed. Cir. 2006); Shyface v. Sec’y of Health
& Human Servs., 165 F.3d 1344, 1352 (Fed. Cir. 1999).

To prove causation for an “off-Table” injury, petitioners must satisfy the three-pronged test
established in Althen v. Sec’y of Health & Human Servs., 418 F.3d 1274 (Fed. Cir. 2005). Althen
requires that petitioners show by preponderant evidence that a vaccination caused his or her injury
“by providing: (1) a medical theory causally connecting the vaccination and the injury; (2) a logical
sequence of cause and effect showing that the vaccination was the reason for the injury; and (3) a
showing of a proximate temporal relationship between vaccination and injury.” Id. at 1278.
Together, these prongs must show “that the vaccine was ‘not only a but-for cause of the injury but
also a substantial factor in bringing about the injury.’” Stone v. Sec’y of Health & Human Servs.,
676 F.3d 1373, 1379 (Fed. Cir. 2012) (quoting Shyface, 165 F.3d at 1352-53).

Each of the Althen prongs requires a different showing. The first Althen prong requires
petitioner to provide a “reputable medical theory” demonstrating that the vaccines received can
cause the type of injury alleged. Pafford, 451 F.3d at 1355-56 (citation omitted).

The second Althen prong requires proof of a “logical sequence of cause and effect.”
Capizzano, 440 F.3d at 1326 (quoting Althen, 418 F.3d at 1278). In other words, even if the
vaccinations can cause the injury, petitioner must show “that it did so in [this] particular case.”
Hodges v. Sec’y of Health & Human Servs., 9 F.3d 958, 962 n.4 (Fed. Cir. 1993) (citation omitted).
“A reputable medical or scientific explanation must support this logical sequence of cause and
effect,” id. at 961 (citation omitted), and “treating physicians are likely to be in the best position
to determine whether a logical sequence of cause and effect show[s] that the vaccination was the
reason for the injury,” Paluck v. Sec’y of Health & Human Servs., 786 F.3d 1373, 1385 (Fed. Cir.
2015) (quoting Andreu, 569 F.3d at 1375).

To satisfy the third Althen prong, petitioner must establish a “proximate temporal
relationship” between the vaccination and the alleged injury. Althen, 418 F.3d at 1281. This
“requires preponderant proof that the onset of symptoms occurred within a timeframe for which,
given the medical understanding of the disorder’s etiology, it is medically acceptable to infer
causation-in-fact.” De Bazan v. Sec’y of Health & Human Servs., 539 F.3d 1347, 1352 (Fed. Cir.
2008).

A petitioner may also be eligible for compensation if the vaccinee had a preexisting
condition that was significantly aggravated by a vaccine. See § 11(c)(1)(C). In considering a
significant aggravation claim for an on-Table injury, the Federal Circuit placed the most
significance on whether petitioner’s symptoms began within the time period prescribed.
Whitecotton v. Sec’y of Health & Human Servs., 81 F.3d 1099, 1107 (Fed. Cir. 1996) (“Instead of
asking whether the person's symptoms would have occurred absent the vaccine, our test hoves (sic)
close to the statutory mandate, and relieves a petitioner of the burden of proving causation if she
can show that the first symptom or manifestation of the significant aggravation of her condition
occurred within the table time period provided in the statute.”).

27
For a significant aggravation claim for an off-Table injury, the petitioner’s burden is
expanded to six elements, requiring petitioner to show, by preponderant evidence,

(1) the person’s condition prior to administration of the vaccine, (2) the person’s
current condition (or the condition following the vaccination if that is also
pertinent), (3) whether the person’s current condition constitutes a “significant
aggravation” of the person’s condition prior to vaccination, (4) a medical theory
causally connecting such a significantly worsened condition to the vaccination, (5)
a logical sequence of cause and effect showing that the vaccination was the reason
for the significant aggravation, and (6) a showing of a proximate temporal
relationship between the vaccination and the significant aggravation.

Loving ex rel. Loving v. Sec’y of Health & Human Servs., 86 Fed. Cl. 135, 144 (2009). The fourth,
fifth, and sixth factors are derived from the Althen prongs. Id. The Federal Circuit has agreed with
this approach. See W.C. v. Sec’y of Health & Human Servs., 704 F.3d 1352, 1357 (Fed. Cir. 2013)
(“We hold that the Loving case provides the correct framework for evaluating off-table significant
aggravation claims.”)

C. Fact Finding

The process for making determinations in Vaccine Program cases regarding factual issues
begins with analyzing the medical records, which are required to be filed with the petition. §
11(c)(2). Medical records created contemporaneously with the events they describe are generally
considered to be more trustworthy. Cucuras v. Sec’y of Health & Human Servs., 993 F.2d 1525,
1528 (Fed. Cir. 1993); but see Kirby v. Sec’y of Health & Human Servs., 993 F.3d 1378, 1382-83
(Fed. Cir. 2021) (clarifying that Cucuras does not stand for proposition that medical records are
presumptively accurate and complete). While not presumed to be complete and accurate, medical
records made while seeking treatment are generally afforded more weight than statements made
by petitioner after-the-fact. See Gerami v. Sec'y of Health & Human Servs., No. 12-442V, 2013
WL 5998109, at *4 (Fed. Cl. Spec. Mstr. Oct. 11, 2013) (finding that contemporaneously
documented medical evidence was more persuasive than the letter prepared for litigation
purposes), mot. for rev. denied, 127 Fed. Cl. 299 (2014). Indeed, “where later testimony conflicts
with earlier contemporaneous documents, courts generally give the contemporaneous
documentation more weight.” Campbell ex rel. Campbell v. Sec’y of Health & Human Servs., 69
Fed. Cl. 775, 779 (2006); see United States v. U.S. Gypsum Co., 333 U.S. 364, 396 (1948).

Despite the weight afforded to medical records, special masters are not bound rigidly by
those records in determining facts such as the onset of a petitioner’s symptoms. Vallenzuela v.
Sec’y of Health & Human Servs., No. 90-1002V, 1991 WL 182241, at *3 (Fed. Cl. Spec. Mstr.
Aug. 30, 1991); see also Eng v. Sec’y of Health & Human Servs., No. 90-175V, 1994 WL 67704,
at *3 (Fed. Cl. Spec. Mstr. Feb 18, 1994) (explaining that § 13(b)(2) “must be construed so as to
give effect to § 13(b)(1) which directs the special master or court to consider the medical
record...but does not require the special master or court to be bound by them”); see also Burns v.
Sec'y of Health & Human Servs., 3 F.3d 415, 417 (Fed. Cir. 1993) (holding that it is within the
special master's discretion to determine whether to afford greater weight to medical records or to

28
other evidence, such as oral testimony surrounding the events in question that was given at a later
date, provided that such determination is rational).

In short, “the record as a whole” must be considered. § 13(a).

D. Evaluating Expert Testimony

Establishing a sound and reliable medical theory connecting the vaccine to the injury often
requires a petitioner to present expert testimony in support of his or her claim. Lampe v. Sec’y of
Health & Human Servs., 219 F.3d 1357, 1361 (Fed. Cir. 2000). The Supreme Court’s opinion in
Daubert v. Merrell Dow Pharmaceuticals, Inc., 509 U.S. 579 (1993), requires that courts
determine the reliability of an expert opinion before it may be considered as evidence. “In short,
the requirement that an expert’s testimony pertain to ‘scientific knowledge’ establishes a standard
of evidentiary reliability.” Id. at 590 (citation omitted). Thus, for Vaccine Act claims, a “special
master is entitled to require some indicia of reliability to support the assertion of the expert
witness.” Moberly ex rel. Moberly v. Sec’y of Health & Human Servs., 592 F.3d 1315, 1324 (Fed.
Cir. 2010). The Daubert factors are used in the weighing of the reliability of scientific evidence
proffered. Davis v. Sec’y of Health & Human Servs., 94 Fed. Cl. 53, 66-67 (2010) (“uniquely in
this Circuit, the Daubert factors have been employed also as an acceptable evidentiary-gauging
tool with respect to persuasiveness of expert testimony already admitted”). Where both sides offer
expert testimony, a special master’s decision may be “based on the credibility of the experts and
the relative persuasiveness of their competing theories.” Broekelschen, 618 F.3d at 1347 (citing
Lampe, 219 F.3d at 1362). And nothing requires the acceptance of an expert’s conclusion
“connected to existing data only by the ipse dixit of the expert,” especially if “there is simply too
great an analytical gap between the data and the opinion proffered.” Snyder ex rel. Snyder v. Sec’y
of Health & Human Servs., 88 Fed. Cl. 706, 743 (2009) (quoting Gen. Elec. Co. v. Joiner, 522
U.S. 136, 146 (1997)).

E. Consideration of Medical Literature

Finally, although this decision discusses some but not all of the literature in detail, the
undersigned reviewed and considered all of the medical records and literature submitted in this
matter. See Moriarty ex rel. Moriarty v. Sec’y of Health & Human Servs., 844 F.3d 1322, 1328
(Fed. Cir. 2016) (“We generally presume that a special master considered the relevant record
evidence even though [s]he does not explicitly reference such evidence in h[er] decision.”);
Simanski v. Sec’y of Health & Human Servs., 115 Fed. Cl. 407, 436 (2014) (“[A] Special Master
is ‘not required to discuss every piece of evidence or testimony in her decision.’” (citation
omitted)), aff’d, 601 F. App’x 982 (Fed. Cir. 2015).

VII. Discussion

The petition alleges only a Table injury of chronic encephalitis resulting from a Tdap
vaccine. See Petition. The preamble of petitioner’s Motion for Ruling on the Record argues a Table
injury of encephalitis. Motion at 1. However, the Motion concludes that the “Tdap vaccination
caused encephalitis which activated [p]etitioner’s temporal lobe epilepsy”, suggesting that the
Tdap vaccine caused a Table encephalitis, which in turn activated a pre-existing condition of

29
epilepsy. Id. at 13. At the time the Motion for Ruling on the Record was filed, the evidence showed
that petitioner suffered from focal seizures prior to her receipt of the subject Tdap vaccine and that
objective testing ruled out encephalitis as discussed repetitively during status conferences. The
experts 69 agree that petitioner has temporal lobe epilepsy. Therefore, if petitioner fails to prove
that she suffered an on-Table encephalitis following her receipt of the Tdap vaccine, she would
then need to prove causation-in-fact under Althen and significant aggravation under Loving to be
found entitled to compensation.

A. Petitioner’s Table Claim

Petitioner alleges she suffered a Table encephalitis within 72 hours of receiving the Tdap
vaccine which resulted in chronic encephalopathy. To prove acute encephalitis, petitioner must
demonstrate evidence of neurologic dysfunction and an inflammatory process in the brain. 42
C.F.R. §100.3(c)(3). The existence of any of the exclusionary criteria for encephalitis, which
includes an underlying malignancy that led to a paraneoplastic encephalitis, an infectious disease
associated with encephalitis, ADEM, or other conditions or abnormalities that would explain her
symptoms, precludes a finding of an on-Table encephalitis. 42 C.F.R. §100.3(c)(3)(ii).

Petitioner argued that her generalized seizures, confusion, and memory loss are evidence
of neurologic dysfunction sufficient to meet the criteria for an on-Table encephalitis. Motion at 9-
11. Further, after the car accident and while in the ER, she had another seizure followed by a post-
ictal state and was diagnosed with transient alteration of awareness and convulsions. Id. at 10. She
argued that the elevated protein level on CSF testing, abnormal edema seen on MRI, and slowing
on EEG constitute evidence of an inflammatory process in the brain. Id. at 10-11; Pet. Ex. 50 at 2-
3.

Respondent argued that petitioner failed to meet the criteria for Table encephalitis. CSF
testing was negative for infectious pathology with a normal white blood cell count, and there was
no suggestion of any inflammatory process. Response at 18-19. Further, petitioner meets the
exclusionary criteria for a Table encephalitis with MRI findings consistent with cortical dysplasia
and better explained by her seizures. Id. at 19.

Dr. Khan and Dr. Eady opined that the Tdap vaccination triggered an inflammatory process
causing encephalitis that “worsened her seizures.” Pet. Ex. 32 at 1; Pet. Ex. 50 at 3. Dr. Khan
opined that the timing post-vaccination, MRI results on December 24, 2015 showing edema with
broad involvement of multiple lobes, and the elevated protein in the CSF were consistent with
encephalitis. No other explanation for petitioner’s condition was found. Pet. Ex. 50 at 2-3.

Dr. Evans disagreed that petitioner had encephalitis, arguing that petitioner had no clinical
symptoms of encephalitis such as fever, headache, cognitive dysfunction, or psychiatric
abnormalities. Resp. Ex. A at 8-9; Resp. Ex. C at 4-5; Resp. Ex. D at 5-6; Pet. Ex. 57; 70 Pet. Ex.
58. 71 The edema seen on the December 24 MRI was the result of petitioner’s seizures on December

69
This statement does not reflect Dr. Nahm’s opinions, as petitioner expressly stated she would not rely on his opinions
to support her Motion. ECF No. 80.
70
Guedes et al., supra note 35.
71
Fan et al., supra note 36.

30
8, not the cause. Resp. Ex. A at 8-9; Resp. Ex. C at 4-5; Resp. Ex. D at 3, 4, 7; Resp. Ex. C Tab
2; 72 Pet. Ex. 61. 73 The mildly increased protein on CSF testing was due to age and, more
importantly, the CSF revealed normal white and red blood cell count which “strongly mitigates
against encephalitis.” Resp. Ex. A at 8, 9; Resp. Ex. D at 6; Resp. Ex. A Tab 5. 74 Thus, in addition
to a lack of symptoms, there are no objective findings to support a diagnosis of encephalitis.

Dr. Khan and Dr. Eady were petitioner’s treating physicians, but their involvement in her
care was limited and came well after the events in December of 2015. As such, their opinions are
not entitled to the same level of deference given to treating physicians who are familiar with
petitioners both before and after their alleged vaccine injury. Nuttall v. Sec’y of Health & Human
Servs., 122 Fed. Cl. 821, 832 (2015) (“The reasoning underlying the finding that opinions of
treating physicians should be given particular weight does not apply when, as here, the treating
physician only saw the patient after the injury and based his opinion on the same evidence as relied
upon by the retained experts.”), aff’d, 640 F. App’x 996 (Fed. Cir. 2016). While their opinions are
duly considered in light of both Drs. Khan and Eady having the benefit of evaluating and treating
petitioner at some point in the course of her care, their opinions are not binding or beyond reproach.
See also § 13(b)(1); Snyder, 88 Fed. Cl. at 746 n.67 (“there is nothing ... that mandates that the
testimony of a treating physician is sacrosanct—that it must be accepted in its entirety and cannot
be rebutted”).

Dr. Khan saw petitioner once on May 9, 2016. He conducted the 48-hour EEG and
reviewed the results. Pet. Ex. 50 at 1. Dr. Eady took over petitioner’s neurological care in July of
2020, nearly five years after the subject vaccine. Pet. Ex. 32. Both based their opinions on the Tdap
vaccine having caused an encephalitis, which was contrary to the opinions of the treating
physicians who cared for petitioner in December of 2015, the contemporaneous medical records,
and the objective testing. The December 24, 2015 MRI was interpreted by the radiologist as
showing edema in the temporal lobes that “given [her] history”, “may be related to seizure activity”
but added that encephalitis could not be excluded and required clinical correlation with CSF
analysis. Pet. Ex. 3 at 106-07; see also Pet. Ex. 29 at 60 (initial visit with Dr. Eady on July 16,
2020 with assessment including among other considerations “ictal sequela”). The EEG performed
that day was “mildly abnormal [] with left temporal slowing . . . nonspecific and most often
associated with vascular disease. No epileptiform potentials or electrographic seizures” were
identified. Pet. Ex. 3 at 112-13. CSF analysis was done that same day and revealed “mildly”
elevated protein at 45 with reference range of 15-40 mg/dL and a normal red cell count and normal
white blood cell count of 1 with reference range of 0-5. Id. at 11, 15, 18, 122, 125. The discharging
physician wrote that petitioner “appear[ed] remarkably well,” and there was “low clinical
suspicion for acute infectious etiology.” She was discharged and told to follow up with neurology.
Id. at 10, 121.

Dr. Elkayam, the treating neurologist at that time, advised petitioner that there was no
herpes encephalitis, no infection, and no cancer cells in the CSF. Pet. Ex. 3 at 137, 140. Dr.
Elkayam’s record for petitioner’s visit on January 6, 2016 included that her test results, specifically

72
Kim et al., supra note 49.
73
Rogalewski et al., supra note 39.
74
Breiner et al., supra note 57.

31
CSF testing and other laboratory work, were negative/unremarkable and that the EEG was
consistent with the MRI findings. Id. at 157. Dr. Elkayam’s assessment was abnormal brain MRI,
seizure disorder, and unspecified convulsions. Id. at 160, 167. There was no reference to the Tdap
vaccination.

Repeat imaging on January 11, 2016 revealed near normal findings on MRI with prior
edema signal in the temporal lobes almost resolved and mildly abnormal EEG with background
frequencies a little slower than expected for an adult, clinically correlated with “mild nonfocal
cortical dysfunction, which could be . . . late residual of a convulsion.” Pet. Ex. 3 at 175, 185-86,
191-92. Paraneoplastic panel antibodies were also normal. Id. at 211-12.

Petitioner herself acknowledged the negative findings of encephalitis in an email to Dr.
Short where she advised that encephalitis was ruled out by lumbar puncture which “tested for
everything from cancer cells to Lyme, West Nile, herpes encephalitis, and even syphilis of the
brain”, and “[e]verything came back clear except for a slightly elevated protein level.” Dr. Short’s
office responded, stating in part that it sounded like a viral meningitis not from the vaccine. Pet.
Ex. 4 at 43. Petitioner’s daughter also affirmed that they were told “there was no significant sign
of encephalitis or otherwise” on the testing from December 24, 2015. Pet. Ex. 26 at 2.

Petitioner’s later medical records repeat a past medical history of
encephalopathy/encephalitis, despite the objective testing ruling it out. Pet. Ex. 3 at 211-12, 255
(Dr. Elkayam informing petitioner on January 18, 2016 that the paraneoplastic panel antibodies
that tested for limbic encephalitis came back negative and labs were normal); Pet. Ex. 50 at 2 (Dr.
Khan’s interpretation of EEG results as focal epilepsy while also referencing the CSF and
paraneoplastic panel that ruled out encephalitis). Other records include a history of encephalitis
reported by petitioner. Pet. Ex. 6 at 64 (presentation to a new PCP on May 26, 2017 reporting a
medical history of arthritis, lipoma, seizures and encephalitis due to HSV”); Pet. Ex. 43 at 84, 88-
89, 91, 93-94 (hospital record from July 12, 2019 containing a history of seizures and encephalitis
secondary to HSV). The perpetuation of a diagnosis in electronic records that has been ruled out
is not persuasive evidence of a diagnosis of encephalitis in this case.

Petitioner did not present with or suffer from any of the clinical symptoms of encephalitis.
She was not diagnosed with or treated for encephalitis, and encephalitis was ruled out by objective
testing. Further, petitioner was suffering from focal seizures prior to her receipt of the Tdap
vaccination and was ultimately diagnosed with cortical dysplasia, which is a recognized cause of
epilepsy, thus excluding her claim from a Table encephalitis. 42 C.F.R. §100.3(c)(3)(ii). For these
reasons, the evidence does not show that petitioner suffered a Table injury as alleged.

B. Petitioner’s Off-Table Claim

Having failed to provide preponderant evidence of a Table encephalitis, the analysis could
end here. ECF No. 1. However, because petitioner’s moving papers imply a causation-in-fact claim
that the Tdap vaccination on December 5, 2015 caused or worsened her epilepsy, it will be
addressed.

32
To satisfy Althen Prong 1 / Loving Prong 4, petitioner must provide a sound and reliable
medical theory as to how the Tdap vaccine could cause or significantly aggravate symptoms.
Althen Prong 2 / Loving Prong 5 requires proof of a logical sequence of cause and effect, usually
supported by facts derived from a petitioner’s medical records. Althen, 418 F.3d at 1278;
Capizzano, 440 F.3d at 1326; Grant v. Sec’y of Health & Human Servs., 956 F.2d 1144, 1148 (Fed.
Cir. 1992). Althen Prong 3 / Loving Prong 6 requires a showing of a proximate temporal
relationship between the vaccination and the significant aggravation. Loving, 86 Fed. Cl. at 144.

Petitioner’s proposed theory is that the Tdap vaccine caused inflammation that resulted in
encephalitis, seizures, and ultimately temporal lobe epilepsy. Pet. Ex. 32 at 1; Pet. Ex. 50 at 2, 3.
In other words, the theory relies on the presence of encephalitis. Broekelschen, 618 F.3d at 1346;
Lombardi, 656 F.3d at 1353. However, encephalitis was ruled out by objective testing. Pet. Ex. 3
at 157. Therefore, petitioner must provide a sound and reliable theory for how the Tdap vaccine
caused or worsened her temporal lobe epilepsy within a medically reasonable time post-vaccine.
The difficulty is that petitioner did not proffer such a theory that directly linked the subject vaccine
to the development or progression of her epilepsy.

Dr. Khan opined that the Tdap vaccine triggered a “complex cascade of immunological
activations”, including the production of inflammatory mediators like cytokines that directly affect
neuronal function and excitability, leading to seizures. Pet. Ex. 50 at 3-4; Pet. Ex. 53; 75 Pet. Ex.
54; 76 Pet. Ex. 55. 77 When there is brain inflammation, the blood-brain-barrier is disrupted and may
allow inflammatory mediators to enter the brain, increasing the risk of seizures and disease
progression of epilepsy. Pet. Ex. 50 at 4; Pet. Ex. 56. 78 Dr. Eady submitted that she bases
petitioner’s treatment on this explanation of her “disease course.” Pet. Ex. 32 at 1. Dr. Ramsay’s
assessment was “DPT reaction” and “[p]rovoked seizure – the temporal relationship of the DPT
shot and the seizure and the MRI changes suggest the seizure was from a reaction to the DPT,”
with follow up MRI showing resolution of changes. Pet. Ex. 3 at 263.

Dr. Khan provided Herve to show that vaccines result in the production of cytokines and
inflammatory mediators. However, Herve does not discuss the ability of cytokines to cross the
blood-brain barrier, cause damage, worsen seizures, or trigger epilepsy. Pet. Ex. 53. 79 Similarly,
Dr. Khan relied on Vezzani, asserting that the study showed that cytokines contribute in some way
to neuronal excitability of underlying seizures, but this discussion was in the context of
“inflammatory processes [that] are induced in [the] brain following infection, neurotrauma, stroke,
febrile seizures, [and] status epilepticus”; Vezzani does not discuss vaccination or explain how
cytokines can contribute to or cause afebrile seizures or epilepsy. Pet. Ex. 55 at 2. 80 Furthermore,
petitioner did not address whether the cytokines produced in response to vaccination, specifically
Tdap vaccination, are the same as or different from those produced in response to other
inflammatory challenges.

75
Hervé et al., supra note 31.
76
Baldelli et al., supra note 33.
77
Vezzani et al., supra note 32.
78
van Vliet et al., supra note 34.
79
Hervé et al., supra note 31.
80
Vezzani et al., supra note 32.

33
Dr. Khan relied on Chang as support for adverse reactions to Tdap vaccine, including
seizures. Chang used VAERS, the U.S. passive surveillance system for adverse events, and
included the many limitations of VAERS such as underreporting, incomplete information,
inadequate data, and lack of an unbiased comparison group. The authors note that “[c]ausality
between reported [adverse events] and vaccines cannot usually be assessed from individual reports
to VAERS.” Pet. Ex. 51 at 2, 5. 81 The authors further concluded that their surveillance summary
was “reassuring” of the safety of Tdap in all age groups. Id. at 5. Chang also cited to the 2012
Institute of Medicine report on causality of vaccine adverse events, which concluded that “the
evidence is inadequate to accept or reject a causal relationship” between Tdap and seizures, among
others. Id. at 2.

Dr. Khan also relied on Sun, which found a small increased risk of “febrile” seizures on
the day of the first two DTaP-IPV-Hib vaccinations at 3 and 5 months of age but no increased risk
of epilepsy. Sun did not discuss afebrile seizures. Pet. Ex. 52 at 1. 82

Respondent argued that the literature does not show an association between vaccination
and poor neurological outcomes. Resp. Ex. A at 9; Resp. Ex. A Tab 6. 83 Dr. Evans acknowledged
a concern for seizures post-vaccination resulting from fever which may lower seizure threshold.
Resp. Ex. A at 9-10. But Haberg, Barlow, and Vestergaard all show that neither vaccinations nor
febrile seizures after vaccinations are associated with an increased risk of epilepsy. Id. at 10; Resp.
Ex. A Tab 3; 84 Resp. Ex. A Tab 12; 85 Resp. Ex. A Tab 17. 86

Dr. Khan and Dr. Eady failed to provide any explanation beyond a conclusory theory that
the Tdap vaccine can “rev[] up the disease process” of epilepsy via an inflammatory process that
breached the blood brain barrier, causing encephalitis and temporal lobe epilepsy. Drs. Khan and
Eady did not acknowledge or explain how this theory applies to this case in the context of pre-
existing focal seizures, afebrile seizures, and cortical dysplasia, which a known cause of epilepsy.
Furthermore, they did not explain how their theories involving an inflammatory process apply here
where there are no clinical symptoms of fever, headache, or illness. Still further, petitioner’s treater
Dr. Ramsay concluded that petitioner suffered from a “DPT reaction”, though petitioner received
a Tdap vaccination, not a whole cell DPT vaccine. Additionally, Dr. Ramsay’s medical records do
not include petitioner’s history of absence seizures prior to receipt of the Tdap vaccination,
rendering his opinions questionable as to whether he was aware of the prior history of seizures
before reaching his conclusion. In sum, petitioner provided no persuasive evidence that
vaccinations can cause afebrile seizures or cause or aggravate epilepsy or that the Tdap vaccination
did so in this case.

81
Chang et al., supra note 29.
82
Sun et al., supra note 30.
83
Brown et al., supra note 58.
84
Barlow et al., supra note 62. Barlow discussed febrile seizures following whole cell DTP and MMR vaccines, but
neither vaccine was associated with an increased risk of afebrile seizures.
85
Haberg et al., supra note 63.
86
Vestergaard et al., supra note 64.

34
While cortical dysplasia was not discussed at all by Drs. Khan, Eady, or Ramsay, the
literature filed by petitioner discusses it in the context of temporal lobe epilepsy. Pet. Ex. 21; 87 Pet.
Ex. 22; 88 Pet. Ex. 24. 89 Cortical dysplasia is described as a malformation of cortical development
and is the most common cause of epilepsy in children and second or third most common cause of
epilepsy in adults. Pet. Ex. 21 at 1; Pet. Ex. 22 at 1. There are three classifications of cortical
dysplasia, one of which presents with mild symptoms, has late onset in adulthood, and is associated
with changes in the temporal lobe. Pet. Ex. 21 at 1. Unless the focal cortical dysplasia area is large,
patients do not have severe neurological deficits, and the main clinical manifestation is epilepsy.
Pet. Ex. 22 at 2. Déjà vu is frequently studied in the context of temporal lobe epilepsy and is
described as a “nebulous mental experience—a mismatch between subjective perceptions of
memory and retrieval itself.” Pet. Ex. 24 at 1.

In her Motion, petitioner proposed for the first time a two-hit theory with cortical dysplasia
as the “first hit” and the Tdap vaccine the “second hit.” Motion at 16. She relied on two prior cases
in which this theory was successful. However, those two cases are distinguishable from the instant
case. The infant in Heilig had an underlying cortical dysplasia. She received DTaP, hep B, IPV,
Hib, rotavirus, and PCV vaccines at her six-month well child visit, then had a 30-minute febrile,
tonic-clinic seizure the following day. She also tested positive for RSV. The special master found
the petitioner’s theory—that the vaccines she received caused her to develop a fever, which in turn
triggered a febrile seizure and lowered the seizure threshold and acted as the “second hit” of the
child’s cortical dysplasia, ultimately triggering epilepsy—to be persuasive. Heilig, No. 16-140V,
2024 WL 929030. In Reilly, the special master accepted the petitioner’s theory that the pertussis
component of the DTaP vaccine administered to an infant at his six-month well child visit acted
as the “second hit” in triggering his epilepsy disorder, in the context of a lower seizure threshold
due to underlying cortical dysplasia and fever present at the time of vaccination. Reilly, No. 09-
489V, 2016 WL 3456844. In other words, both Heilig and Reilly involved infants who had a fever
or febrile seizures. In this case, there is no evidence that petitioner had a fever or febrile seizure at
any point after receiving the subject vaccine.

Furthermore, the two-hit theory has been found unpersuasive in other afebrile seizure
cases, including in one before the undersigned. Gram v. Sec’y of Health & Human Servs., No. 15-
515V, 2022 WL 17687972 (rejecting a two-hit theory in the context of an afebrile seizure and
epilepsy); Akers, No. 15-597V, 2021 WL 3560069.

Regardless, a two-hit theory was not sufficiently articulated in this case to satisfy
petitioner’s burden under Althen Prong 1 / Loving Prong 4. Further, this theory is at odds with her
treaters’/experts’ opinions who did not address the cortical dysplasia as contributory, despite
several discussions at status conferences that this would be necessary. ECF Nos. 38, 40, 55, 71. In
fact, Dr. Khan went so far as to deny that any other etiology was present that could account for
petitioner’s condition, essentially rejecting a purported “first hit.” Pet. Ex. 50 at 3. While Dr. Evans

87
Joanna Kabat & Przemystaw Krol, Focal cortical dysplasia – review, 77 Polish J. of Radiology 35 (2012), filed as
“Pet. Ex. 21.”
88
Blumcke et al., supra note 6.
89
Chris J.A. Moulin, The strange sensation of déjà vu: not so strange in temporal lobe epilepsy, 85 J. of Neurology,
Neurosurgery, and Psychiatry 132 (2014), filed as “Pet. Ex. 24.”

35
was not afforded an opportunity to address the late proposed two-hit theory, that is of no
consequence. The two-hit theory was unsupported and was a rather last minute “Hail Mary.”

In sum, petitioner failed to provide a sound and reliable theory for how the Tdap vaccine
can cause or worsen afebrile seizures or temporal lobe epilepsy and therefore has failed to satisfy
Althen Prong 1 / Loving Prong 4.

As to the remaining Loving Prongs, it is impossible to determine whether petitioner’s
seizures worsened from what they were prior to the Tdap vaccine. Seizures commonly associated
with cortical dysplasia include complex partial seizures, generalized complex partial seizures,
simple partial seizures, generalized tonic clonic seizures—some with auras, and nocturnal seizures.
Resp. Ex. A Tab 16 at 1. 90 Throughout the evidence filed in this case, petitioner reported “déjà vu”
episodes before and after receipt of the Tdap vaccine, a term of art commonly used to describe
experiences of patie

[Text truncated at 120,000 characters. The full text is on the page linked above.]

---

Source: Frix Law Library, https://www.frixlaw.com/law-library/cases/11343331. Public record. Not legal advice.