Nieves v. Secretary of Health and Human Services ( 2021 )


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  •                   In the United States Court of Federal Claims
    OFFICE OF SPECIAL MASTERS
    No. 18-1602V
    (Not to be published)
    *************************
    *
    ANDRES NIEVES,              *
    *
    *                                             Filed: January 11, 2021
    Petitioner, *
    *
    v.                *
    *
    SECRETARY OF HEALTH AND     *
    HUMAN SERVICES,             *
    *
    Respondent. *
    *
    *************************
    Michael Adly Baseluos, Baseluos Law Firm, PLLC, San Antonio, TX, for Petitioner.
    Mary Eileen Holmes, U.S. Dep’t of Justice, Washington, DC, for Respondent.
    ORDER DISMISSING TABLE CLAIM (PARTIAL DISMISSAL OF CASE) 1
    On October 17, 2018, Andres Nieves filed a petition seeking compensation under the
    National Vaccine Injury Compensation Program (the “Vaccine Program”) 2 alleging that he
    suffered Guillain-Barré syndrome (“GBS”) caused by his receipt of the influenza (“flu”) vaccine
    on October 28, 2015. Petition (ECF No. 1) at 1. Respondent reacted by filing a Rule 4(c) Report
    on November 8, 2019, maintaining that this case is not appropriate for compensation. ECF No. 22.
    Because I find that (based both on the undisputed facts as well as admissions by Petitioner’s expert)
    1 Although, I have not designated this for publication, because this Order contains a reasoned explanation for my
    actions in this case, it will be posted on the United States Court of Federal Claims website, in accordance with the E-
    Government Act of 2002, 44 U.S.C. § 3501 (2012). As provided by 42 U.S.C. § 300aa-12(d)(4)(B), however, the
    parties may object to the Order’s inclusion of certain kinds of confidential information. Specifically, under Vaccine
    Rule 18(b), each party has fourteen days within which to request redaction “of any information furnished by that party:
    (1) that is a trade secret or commercial or financial in substance and is privileged or confidential; or (2) that includes
    medical files or similar files, the disclosure of which would constitute a clearly unwarranted invasion of privacy.”
    Vaccine Rule 18(b). Otherwise, the whole Order will be available to the public.
    Id. 2
     The Vaccine Program comprises Part 2 of the National Childhood Vaccine Injury Act of 1986, Pub. L. No. 99-660,
    100 Stat. 3758, codified as amended at 42 U.S.C. §§ 300aa-10 through 34 (2012) (“Vaccine Act” or “the Act”).
    Individual section references hereafter will be to § 300aa of the Act (but will omit that statutory prefix).
    the Table version of the claim cannot succeed, I hereby dismiss it—although this does not
    constitute the end of the case entirely.
    I.     Factual Background and Medical History
    A. Petitioner’s Pre-Vaccination Medical History
    Before Mr. Nieves ever received the vaccination that is the basis for his claim, he had
    visited healthcare professionals complaining of symptoms similar to those he alleges resulted from
    the vaccination. Mr. Nieves has a past medical history significant for sinusitis, fibromyalgia
    rheumatica with myositis, obesity, status post-lap band surgery, anxiety, cervical spinal stenosis
    with related radiculopathy, and right carpal tunnel syndrome. Ex. 2 at 2 –4; Ex. 3 at 3 –121; Ex. 4
    at 1 –222 ; Ex. 7 at 1 –22. He had been prescribed Gabapentin and Robaxin for his symptoms which
    provided little relief. Ex. 2 at 29. In 2013, Mr. Nieves saw a neurosurgeon with complaints of pain
    radiating to both shoulders and arms with sensations of heaviness, weakness, numbness, and
    tingling.
    Id. at 2
    9 
    –30. This was associated with some difficulty buttoning shirts, tying shoes, and
    accompanied by frequent falling.
    Id. B. October 2015
    Flu Vaccination and Subsequent Medical History
    On October 28, 2015, Mr. Nieves received a seasonal flu vaccine in his right arm. Ex. 1 at
    10. That same day, he reported feeling “feverish and a little achy.” Affidavit, filed as Ex. 18 (ECF
    No. 36-1) at 2. The next day (October 29, 2015), Mr. Nieves reported “waking up with general
    malaise and flu like symptoms with some aches and pains all over [] [his] body.”
    Id. Petitioner presented to
    his primary care physician with complaints of a mild allergic response four hours after
    receiving the flu shot. Ex. 5 at 20. He was advised to take ibuprofen and diazepam, with follow-
    up as needed.
    Id. On October 31,
    2015 (three days post-vaccination), Mr. Nieves reported experiencing a
    different kind of symptom. Now, he maintained that he had begun “feeling strange” and noticed
    that his “walking was a little different.” Affidavit at 2. He also reports that he began losing some
    sensation in his hands and feet later on that day.
    Id. On November 2,
    2015, Mr. Nieves reported to the emergency room with complaints of
    fatigue, leg pain and lower back pain with an onset five days prior (or on October 28 th). Ex. 3 at
    89 –90. The next day (November 3, 2015), he was seen by neurologist Dr. Anna Marieta Moise,
    complaining of a “one-week history of paresthesia’s” in his distal extremities since he got his flu
    shot.
    Id. at 86
    –88. Dr. Moise’s exam showed normal strength and reflexes.
    Id. at 86
    . Dr. Moise’s
    assessment was paresthesias most likely due to nutritional deficiencies and planned treatment to
    supplement.
    Id. Another treater during
    this visit, Ethelyn D. Johnson, MD, noted “doubt guillan
    [sp] barre syndrome (GBS) PT [patient] has good strength on exam, gait minimally impaired,
    reflexes +1 bilat.”
    Id. at 89. 2
            On November 4, 2015, Mr. Nieves returned to the emergency room with worsening back
    pain and generalized weakness. Ex. 3 at 76 –77. Mr. Nieves also indicated he previously had
    difficulty walking.
    Id. He was given
    pain medications.
    Id. On November 9,
    2015, Mr. Nieves again
    returned to the emergency room, reporting worsening low back pain radiating up to his neck and
    shoulders and down to his lower extremities. Ex. 3 at 67 –69. He was assessed with chronic back
    pain, and it was again proposed that his condition was unlikely a primary neurological problem
    like GBS or cord compression.
    Id. On November 10,
    2015, Mr. Nieves returned to his primary care physician complaining of
    weakness, fatigue, and generalized muscle pain after getting the flu vaccine. Ex. 5 at 1. He was
    referred to the emergency department for further evaluation and neurology care.
    Id. at 7.
    Later that
    day, Mr. Nieves was admitted to the hospital for weakness and concerns for GBS. Ex. 3 at 65. A
    lumbar puncture showed mildly elevated protein after which Mr. Nieves was diagnosed with GBS
    and treated with IVIG.
    Id. He improved and
    was discharged 10 days later, on November 20, 2015
    with a treatment plan to continue physical therapy (“PT”) and occupational therapy (“OT”)
    Id. Diagnosis at discharge
    was GBS. Ex. 6 at 107 –117; 122 –125; 150–154.
    C. Petitioner’s Ongoing Symptoms and Change in Diagnosis
    Two months later, on January 8, 2016, Mr. Nieves was seen by a neurologist. Dr. Adetoun
    Musa. Ex. 3 at 44 –48. Mr. Nieves indicated he was now having worsening paresthesias, balance
    issues, and that his weakness had not improved with PT/OT, or since his prior IVIG treatment in
    November the prior year.
    Id. at 45.
    Dr. Musa expressed concern for underlying chronic
    inflammatory demyelinating polyneuropathy (“CIDP”) given the prolonged duration of symptoms.
    Id. at 47.
    On February 8, 2016, Mr. Nieves underwent an EMG which showed generalized
    sensorimotor polyneuropathy, which was predominately demyelinating in type and mild in degree.
    Ex. 3 at 43. These findings were deemed to be consistent with an acquired segmental
    demyelinating polyneuropathy, like that seen in CIDP and related disorders.
    Id. On February 11,
    2016, Mr. Nieves returned to Dr. Musa who noted the EMG had shown findings consistent with
    CIDP.
    Petitioner continued to receive treatment for CIDP for the remainder of 2016. See, e.g., Ex.
    3 at 15 –18, and Ex. 8 at 6 –80. However, follow-up EMG tests performed in the fall of 2016 did
    not confirm the condition, or any demyelinating neuropathy for that matter. Ex. 11 at 63 –65. The
    most recent EMG performed on Petitioner showed no CIDP, and treaters instead attributed Mr.
    Nieves’s pain and cramps to fibromyalgia.
    Id. II.
       Procedural History
    As noted above, the case was initiated in October 2018, and it was originally assigned to
    Special Master Roth. After Respondent indicated his intent to contest entitlement, Petitioner filed
    3
    an expert report and supporting medical literature. Report, dated Feb. 6, 2020, filed as Ex. 17 (ECF
    No. 23-2) (“Kinsbourne First Rep.”). The parties were subsequently ordered to file briefs regarding
    the disputed issue of onset of Petitioner’s symptoms. See Order, May 1, 2020 (ECF No. 30). While
    such filings were pending, this case was reassigned to me. See Docket Entry, July 20, 2020 (ECF
    No. 32).
    On September 9, 2020, Petitioner filed a status report confirming his view that he had a
    viable Table claim for GBS caused by the flu vaccine, and therefore sought Respondent’s input on
    whether the claim could be settled as such. See Status Report, filed Sept. 9, 2020 (ECF No. 37).
    On September 28, 2020 Respondent reacted to this contention, disputing that Petitioner’s Table
    claim was proper, and requesting a finding of onset no later than one day post-vaccination. See
    Resp.’s Onset Brief (ECF No. 39). Respondent also noted inconsistencies in Petitioner’s brief and
    expert report as well as the contemporaneous medical record.
    Id. at 1.
    Petitioner responded with a
    rebuttal memorandum on November 16, 2020 and filed additional supporting documents including
    a supplemental expert report. See Pet.’s Response Brief (ECF No. 41-1); Report, dated Nov. 16,
    2020, filed as Ex. 20 (ECF No. 41-3) (“Kinsbourne Supp. Rep.”).
    ANALYSIS
    To receive compensation under the Vaccine Program, a petitioner must prove either: (1)
    that she suffered a “Table Injury”—i.e. an injury falling within the Vaccine Injury Table—
    corresponding to one of the vaccinations in question, or (2) that her illnesses were actually caused
    by a vaccine (a “non-Table injury”). See §§ 300aa-13(a)(1)(A),11(c)(1); § 300aa-14(a), as
    amended by 42 C.F.R § 100.3; 300aa-11(c)(1)(C)(ii)(I); see also Moberly v. Sec’y of Health &
    Human Servs., 
    592 F.3d 1315
    , 1321 (Fed. Cir. 2010); Capizzano v. Sec’y of Health & Human
    Servs., 
    592 F.3d 1317
    , 1320 (Fed. Cir. 2006).3
    For both Table and Non-Table claims, Vaccine Program petitioners bear a “preponderance
    of the evidence” burden of proof. Section 13(1)(a). That is, a petitioner must offer evidence that
    leads the “trier of fact to believe that the existence of a fact is more probable than its nonexistence
    before [he] may find in favor of the party who has the burden to persuade the judge of the fact's
    existence.” 
    Moberly, 592 F.3d at 1322
    n.2; see also Snowbank Enter. v. United States, 
    6 Cl. Ct. 476
    , 486 (1984) (mere conjecture or speculation is insufficient under a preponderance standard).
    Proof of medical certainty is not required. Bunting v. Sec'y of Health & Human Servs., 
    931 F.2d 867
    , 873 (Fed. Cir. 1991). In particular, a petitioner must demonstrate that the vaccine was “not
    only [the] but-for cause of the injury but also a substantial factor in bringing about the injury.”
    3
    Decisions of special masters (some of which I reference in this ruling) constitute persuasive but not binding authority.
    Hanlon v. Sec’y of Health & Human Servs., 
    59 Fed. Cl. 121
    , 124 (2003), aff’d, 104 F. App’x 712 (Fed. Cir. 2004);
    see also Spooner v. Sec. of Health & Human Servs., No. 13-159V, 
    2014 WL 504728
    , at *7 n.12 (Fed. Cl. Spec. Mstr.
    Jan. 16, 2014).
    4
    
    Moberly, 592 F.3d at 1321
    (quoting Shyface v. Sec'y of Health & Human Servs., 
    165 F.3d 1344
    ,
    1352-53 (Fed. Cir. 1999)); Pafford v. Sec'y of Health & Human Servs., 
    451 F.3d 1352
    , 1355 (Fed.
    Cir. 2006). A petitioner may not receive a Vaccine Program award based solely on his assertions;
    rather, the petition must be supported by either medical records or by the opinion of a competent
    physician. Section 13(a)(1).
    Here, it is not completely clear whether Petitioner seeks to establish a Table claim.
    However, the Petition clearly alleges that that he suffered from “Guillan-Barre [sic] Syndrome
    (GBS) secondary to symptoms of ataxia (i.e. difficulties with balance), ascending paralysis of the
    lower extremities proximally up above the waist and to a lesser degree in the upper extremities
    resulting in IVIG; severe constipation; and disabling fatigue, which was ‘caused-in-fact’ by [the
    flu] vaccination” he received on October 28, 2015, and that he continues to suffer sequelae from
    the injury. Petition at 1. Moreover, in addressing the onset issues raised in the matter, Petitioner
    confirmed his view that he had a viable Table claim, based on his contentions about onset. ECF
    No. 37. It is accordingly appropriate for me to evaluate the factual support for that claim.
    To establish any Table claim, a petitioner must make a precise factual showing sufficient
    to meet the claim’s relevant definitions, as set forth in the Table’s “Qualifications and aids to
    interpretation” (“QAIs”). Section 14(b). If successful, the petitioner need not also demonstrate
    vaccine causation, as it is presumed if the Table requirements for a particular claim are met. Section
    14(a). To establish a GBS Table Injury, a petitioner must prove that the onset of symptoms was no
    less than three days and no more than forty-two days after vaccine administration. 42 C.F.R. §
    100.3(a)(XIV)(D). Moreover, a petitioner must also demonstrate that there is no more likely
    diagnosis for his symptoms. See C.F.R. § 100.3(c)(15)(v). An ultimate diagnosis of CIDP is
    considered an exclusionary criterion for a flu-GBS claim. Section 14(b).
    In this case, onset is not a basis for dismissal, given the medical record and filings.
    Respondent correctly observes that contemporaneous medical records establish that Petitioner
    began experiencing some kind of initial symptoms either the day of or the day following
    vaccination. Resp.’s Onset Brief at 6. Had these symptoms been deemed an initial presentation of
    GBS, a Table claim would not be tenable, since onset cannot be sooner than three days post-
    vaccination.
    But Petitioner has convincingly demonstrated reason to distinguish his immediate, same-
    day symptoms from those that later could be deemed to be neuropathic in nature, with the former
    more evidence of a transient, non-specific vaccine reaction. Pet.’s Response Brief at 2. In support,
    Petitioner points to a medical record dated November 2, 2015 (five days post-vaccination) in which
    he expressed to treaters that he was (as of that date) experiencing leg and lower back pain. Ex. 3
    at 89 –90. By contrast, he has alleged feeling feverish and achy as of the day he received the
    vaccine—and indeed he sought treatment not long after for a mild allergic response to the
    vaccination. Ex. 5 at 20. As Dr. Kinsbourne observed, moreover, there are a number of symptoms
    that medicine recognizes can follow receipt of the flu vaccine, including soreness, redness and
    5
    swelling, fever, muscle aches, and headaches. Kinsbourne Supp. Rep. at 1-2 (citing Center for
    Disease Control (2019)). Mr. Nieves otherwise did not present with symptoms of progressive
    tingling, numbness, and frequent falls until November 9, 2015.
    Id. at 5
    (citing Ex. 3 at 70).
    Accordingly, it is not more likely than not that Petitioner’s onset of neuropathic symptoms began
    outside the Table’s 3 –42 day post-vaccination timeframe.
    However, Petitioner cannot meet the QAI diagnostic requirement for a flu-GBS Table
    claim—because the record preponderantly establishes that Petitioner’s ultimate diagnosis was
    CIDP. At most, the record reveals that treaters initially believed that GBS was the proper diagnosis
    at the time of Petitioner’s initial presentation. But the same record also reveals that by January
    2016 (approximately two months post-onset), Petitioner was continuing to experience
    neurologic/neuropathic symptoms—and treaters began to propose (based on a longer history) that
    CIDP rather than GBS best explained his symptoms. This is consistent with the fact that GBS is
    known to be acute and monophasic—not chronic and meandering like CIDP. Under such
    circumstances, it is proper to conclude that CIDP best explains a claimant’s injury, even if treaters
    (based on far less data) initially understood the presenting symptoms to be GBS. Blackburn v.
    Sec’y of Health & Human Servs., No. 10-410V, 
    2015 WL 425935
    (Fed. Cl. Spec. Mstr. Jan. 9,
    2015).
    My conclusion is also supported by Petitioner’s expert in this case. Dr. Kinsbourne has
    opined that “Mr. Nieves had a polyneuropathy, which was first diagnosed as Guillain-Barre
    syndrome but as it evolved turned out to be CIDP.” Kinsbourne Rep. at 5 (emphasis added). He
    bases his opinion on the fact that the treating neurologists thus diagnosed him, both on clinical
    grounds and based on electrodiagnostic and cerebrospinal fluid findings” with CIDP.
    Id. Further, the electrodiagnostic
    test results in February 2016 removed any doubt that Petitioner was suffering
    from CIDP.
    Id. at 6.
    And Dr. Kinsbourne otherwise distinguished GBS, a far more common
    polyneuropathy, from CIDP, whose progression from onset to maximal deficit takes two months
    at least. Kinsbourne First Rep. at 6.
    As a result, any Table claim, to whatever extent it may have been alleged, that the flu
    vaccine caused Petitioner’s GBS, fails in this case and is dismissed. However, the case in its
    entirety is not properly dismissed at this time—because the question of whether the flu vaccine
    can and did cause Petitioner’s alleged CIDP in a medically acceptable timeframe raises a
    reasonable, non-Table/causation-in-fact claim. 4 Such a claim will require Petitioner to establish
    the three prongs of the test set by the Federal Circuit in Althen v. Sec'y of Health & Human Servs.,
    
    418 F.3d 1274
    (Fed.Cir.2005) as well as the propriety of the CIDP diagnosis, which Respondent
    disputes. 5 At this point, Petitioner has already offered expert support for such a non-Table claim.
    4   There is no CIDP/flu vaccine table claim.
    5Respondent argues that the EMG studies undermine the reliability of the initial GBS/CIDP diagnosis. Rule 4(c)
    Report at 8. Thus, although the first EMG showed evidence of CIDP, the second and third tests showed no evidence
    of demyelinating condition.
    Id. And treaters eventually
    concluded that Petitioner’s symptoms were due to
    6
    See Kinsbourne Rep. at 13. Respondent will therefore be offered the opportunity to provide a
    rebutting expert report.
    CONCLUSION
    Petitioner’s flu-GBS Table claim fails because the record preponderantly establishes that
    Petitioner’s ultimate diagnosis was CIDP. Accordingly, Petitioner’s Table claim is hereby
    dismissed. Respondent shall file a status report on or before January 22, 2021, proposing a
    deadline for the filing of an expert report of his own if he wishes to contest the expert opinions
    already offered by Dr. Kinsbourne in support of a non-Table claim that the flu vaccine caused
    Petitioner to experience CIDP.
    IT IS SO ORDERED
    s/Brian H. Corcoran
    Brian H. Corcoran
    Chief Special Master
    fibromyalgia, which had been present since at least 2013.
    Id.
    at 2
    . 
    Respondent cites as additional support two records
    from Petitioner’s treating neurologists who noted that Petitioner’s symptoms did not respond to high dose IVIG or
    steroid treatment.
    Id. at 2
    (citing Ex. 11).
    7