Nichols v. Secretary of Health and Human Services

United States Court of Federal Claims·Decided August 15, 2016·No. 14-1103·Published

Opinion

In the United States Court of Federal Claims OFFICE OF SPECIAL MASTERS No. 14-1103V (To be Published)

************************* * KAYLA NICHOLS and JASON * Special Master Corcoran NICHOLS on behalf of their minor * child, N.N., * * Petitioners, * * Filed: June 22, 2016 v. * * Attorney’s Fees and Costs; SECRETARY OF HEALTH * Reasonable Basis; AND HUMAN SERVICES, * Dismissal Without Hearing; * Reasonable Attorney Time. * Respondent. * * *************************

Andrew D. Downing, Van Cott & Talamante, PLLC, Phoenix, AZ, for Petitioner.

Heather L. Pearlman, U.S. Dep’t of Justice, Washington, DC, for Respondent.

DECISION GRANTING IN PART ATTORNEY’S FEES AND COSTS1

On November 13, 2014, Kayla and Jason Nichols filed a petition on behalf of their minor child, N.N., for compensation in the National Vaccine Injury Compensation Program (the “Vaccine Program”),2 alleging that that the measles-mumps-rubella (“MMR”) and other vaccines

1 Because this decision contains a reasoned explanation for my actions in this case, I will post it 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 decision’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 decision 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, 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. N.N. received on June 3, 2009, and December 13, 2012, caused him to develop neurological issues. See Pet. at 1-2 (ECF No. 1). The claim was dismissed in February of this year, however, after Petitioners failed to meet several deadlines to file an expert report in support of their claim.

Petitioners have now requested an award of attorney’s fees and costs in the combined amount of $21,561.50. App. for Attorney’s Fees & Costs, dated Apr. 12, 2016 (ECF No. 30) (“Fees App.”). Respondent opposes the request, arguing that the claim lacks reasonable basis, and also maintaining in the alternative that the sum requested is too high given the case’s history. For the reasons stated below, I grant in part Petitioners’ request, awarding them $14,490.75 in fees and costs.

Procedural History

As noted above, the case was filed in November 2014. Pet. at 1. The petition expressly stated that N.N. had shown signs of developmental problems after certain childhood vaccinations received in June 2009, and was formally diagnosed with a “neurological condition” by February 2012 that included speech loss and coordination problems. Pet. at 1, 5 ¶15. However, he allegedly showed improvement until December 13, 2012, when he received a new round of MMR and varicella vaccines. Id. at 6 ¶¶ 17, 19. Almost immediately thereafter, he became feverish and displayed other physiologic reactions to the vaccinations, and then many of his neurologic issues returned. Id. at 6-8 ¶¶ 20-26. Petitioners thus alleged that the second MMR dose N.N. received in December 2012 exacerbated symptoms previously thought to have resolved. Id. at 8 ¶¶ 28-29.

The history of counsel’s representation of the Nicholses bears on the present fees request. Four months prior to the petition’s filing, Andrew D. Downing, Esq., and other attorneys and paralegals at the law firm of Van Cott & Talamante, PLLC, were contacted by the Petitioners and began to work on the case. See generally Billing Records, attached as Ex. A to Fee App. at 3-20.3 Prior to the date of the petition’s filing in November, Mr. Downing billed a little over three hours to the matter. Id. at 3. Justin Redman, however, an associate working at Mr. Downing’s firm, billed 14 hours to the matter in the same timeframe (id. at 6-7), and appears to have performed more of the substance review of medical records and the claim’s overall contours. At the same time, two paralegals – Bob Cain and Danielle Avery – collectively performed 8.5 hours of work. Id. at 11- 13.

Overall, this does not reflect a significant effort on counsel’s part to evaluate the case’s strength. Moreover, since the onset of N.N.’s reaction to the MMR vaccine was alleged to have occurred around the time he received it in December 2012, counsel had over a year before the

3 Petitioners did not separately file exhibits to the Fee Application as attachments. Counsel should do so in the future. See Vaccine ECF Rules, Section IV, Filing Requirements, Paragraph 10(a).

2 limitations period would run, and thus faced no pressure to file the petition quickly, before a full analysis of the claim could be made.

Not long after the case’s initiation, the Petitioners filed a large set of medical records relevant to their claim (Notice, dated Nov. 26, 2014 (ECF No. 8)), and then a second set at the end of December, followed by a statement of completion. See Dec. 29, 2014, Statement of Completion (ECF No. 10). In the first several months of 2015, Petitioners filed additional documents identified by Respondent as necessary for evaluation of the case, and then Respondent filed her Rule 4(c) Report on May 28, 2015. ECF No. 17.

In her Rule 4(c) Report, Respondent questioned whether Petitioners could prevail on their claim, given the absence of record evidence of a change in N.N.’s post-December 2012 vaccination condition (along with no clear explanation of what that condition was). ECF No. 17 at 7-8. Rather, the record documented N.N.’s pre-vaccination neurologic problems. Id. at 8. She also noted that the record did not support the allegation that N.N.’s condition had improved prior to the December 2012 MMR vaccine; to the extent Petitioners relied on the statement of Dr. Baxi, one of N.N.’s treaters, to support the allegation, the statement was not corroborated by the actual medical record. Id. at 9. Because of the lack of record support, in a footnote Respondent raised the possibility that the claim lacked a reasonable basis, but she did not elaborate on the point. Id. at 7 n.3.

After review of the Rule 4(c) Report, I scheduled a status conference with the parties for June 2, 2015. At that time, I stated my initial view about problems with Petitioners’ claim, echoing Respondent’s factual points. See Scheduling Order, dated June 2, 2015 (ECF No. 18). But I expressed my understanding of the nature of their claim (that N.N. had somehow experienced a symptomatic relapse after receipt of the MMR vaccine in December 2012), and noted that Petitioners would need an expert to flesh out their theory, and should also contact Dr. Baxi to confirm Mrs. Nichols’s recollection about statements he had made regarding N.N.’s condition. To that end, I set August 31, 2015, as the deadline for Petitioners to submit their expert report. ECF No. 18.

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