Mohamad v. Secretary of Health and Human Services

United States Court of Federal Claims·Decided December 2, 2024·No. 16-1075·Unpublished

Opinion

In the United States Court of Federal Claims

ALA MOHAMAD,

Petitioner, No. 16-1075 v. (Filed Under Seal: November 12, 2024) SECRETARY OF HEALTH AND (Reissued Publicly: December 2, 2024) HUMAN SERVICES,

Respondent.

Richard Gage, Richard Gage, P.C., Cheyenne, Wyoming, for Petitioner. Voris E. Johnson, Jr., Assistant Director, Julia M. Collison, Assistant Director, Heather L. Pearlman, Deputy Director, C. Salvatore D’Alessio, Director, Torts Branch, Brian M. Boynton, Principal Deputy Assistant Attorney General, Civil Division, United States Department of Justice, Washington, D.C., for Respondent.

OPINION AND ORDER1 HADJI, Judge.

Respondent, the Secretary of Health and Human Services, seeks review of Special Master Christian J. Moran’s entitlement ruling and award of compensation in favor of Petitioner, who began suffering from Guillain-Barré Syndrome (GBS) shortly after receiving a tetanus-diphtheria-acellular pertussis (Tdap) vaccine in September 2015. ECF 258. For the reasons stated below, Respondent’s Motion for Review is DENIED, and the Special Master’s Decision is SUSTAINED.

BACKGROUND I. Petitioner’s Medical History As the underlying facts set forth in Petitioner’s medical records are not in dispute, the Court’s recitation of facts draws largely from the Special Master’s entitlement ruling. See ECF 259 at 2; ECF 261 at 8.

1 This Opinion was issued under seal on November 12, 2024. The parties were directed to propose redactions by November 26, 2024. No proposed redactions were received. The Court hereby publicly releases the Opinion and Order in full.

On September 18, 2015, Petitioner received a Tdap vaccine during a routine physical. ECF 150 at 2. Less than two weeks later, he visited a medical facility complaining of numbness in his hands, feet, and lower back. Id. The treating physician diagnosed Petitioner with hyperventilation syndrome. Id.

The next morning, Petitioner fell in his home and was taken to the emergency room where he again complained of numbness. Id. The emergency room doctor diagnosed him with paresthesias of both hands and feet. Id. at 3. Petitioner fell again the next morning. Id. Following tests, including MRIs and a lumbar puncture, Petitioner was diagnosed with GBS and hospitalized for almost the entirety of October 2015. Id. at 3-4. During his stay, two doctors concluded that Petitioner’s GBS was “likely triggered” by his Tdap vaccination. Id. at 3. Petitioner’s internist theorized that Petitioner could have nephritis and noted that his review of literature indicated that glomerulonephritis has been associated with GBS. Id. at 3-4. Petitioner’s internist sought a consult from the nephrology service, which suggested that a kidney biopsy might be needed to reach a definitive diagnosis. Id. at 4. Due to a necessary GBS treatment and the state of Petitioner’s kidney function, Petitioner did not undergo a kidney biopsy. Id. Instead, after reviewing Petitioner’s blood results, one of Petitioner’s doctors theorized that Petitioner’s kidney problem “could potentially be an acute post strep GN [glomerulonephritis].” Id. Despite this speculation, none of Petitioner’s treating physicians diagnosed him with a streptococcus infection. Id.

Near the end of his hospital stay, a different doctor described Petitioner’s chief complaint as “GBS 2/2 [secondary to] Tetanus vaccination.” Id. at 5. Petitioner was discharged from the hospital to a rehabilitation facility on October 30, 2015. Id. at 4-5. In the discharge report, the discharging physician noted that Petitioner “had an allergy to tetanus toxoids and that the allergic reaction produced GBS.”2 Id. at 4.

II. The Petition and Procedural History On August 29, 2016, Petitioner filed a petition seeking compensation under the National Vaccine Injury Compensation Program, 42 U.S.C. §§ 300aa–10-34,3 alleging that his September 2015 Tdap vaccine caused him to develop GBS. ECF 1. In support of his Vaccine Act claim, Petitioner submitted medical records as well as expert reports from neurologist Yuval Shafrir to show that a Tdap vaccine can cause GBS and actually did so in this case. ECF 150 at 5, 7-8 (citing Pet. Ex. 20, ECF 66-1; Pet. Ex. 52, ECF 78-1; Pet. Ex. 58, ECF 90-1; Pet. Ex. 63, ECF 101-1, and Pet. Ex. 64, ECF 101-2). Specifically, in

2 The Special Master noted that Petitioner’s medical record from the Medical Center of Aurora contains several notes about Petitioner’s allergic reaction to the tetanus vaccine. ECF 150 at 4 n.5. He also noted that multiple medical providers recognized that Petitioner developed GBS “following tetanus shot.” Id. 3 The National Vaccine Injury Compensation Program was established by the National Childhood Vaccine Injury Act of 1986, Pub. L. No. 99-660, 100 Stat. 3755 (the Vaccine Act).

his initial expert report, Dr. Shafrir noted that the “[t]etanus vaccine is a known trigger for GBS,” and set forth potential pathophysiological mechanisms by which tetanus toxoid could cause GBS. Pet. Ex. 20 at 14-17, ECF 66-1. In concluding that the Tdap vaccine caused Petitioner’s GBS, Dr. Shafrir primarily relied on case reports of GBS following tetanus-containing vaccines, the temporal association between Petitioner’s Tdap vaccination and the onset of his symptoms, and statements from Petitioner’s treating physicians. See ECF 66-1.

Disputing causation, Respondent offered responsive reports from neuroimmunologist Thomas Leist. Resp’t Ex. B, ECF 76-2; Resp’t Ex. C, ECF 82-1; Resp’t Ex. D, ECF 112-1. In his initial report, Dr. Leist disagreed with the proposition that the Tdap vaccine can cause GBS and in support relied on the 2012 report from the Institute of Medicine (IOM), which concluded that there is insufficient scientific evidence to accept or reject that tetanus-containing vaccines can cause GBS. See Resp’t Ex. B at 4-5, ECF 76-2. Dr. Leist opined that Petitioner’s GBS was not caused by Tdap and theorized that a group A streptococcal infection possibly caused Petitioner’s GBS. Id. at 4, 6-7.

In April 2020, the Special Master introduced two exhibits (the Court Exhibits) into the record. See Court Ex. 1001, ECF 96-1; Court Ex. 1002, ECF 96-2. Both addressed recommendations by the Advisory Committee on Immunization Practices (ACIP), a federal advisory committee chartered to “provide expert external advice and guidance to the Director of [the Centers for Disease Control and Prevention (CDC)] on use of vaccines and related agents for the control of vaccine-preventable diseases.” ECF 96-1 at 3. Court Exhibit 1001 is a CDC weekly report that compiled and summarized the recommendations from ACIP “regarding prevention and control of tetanus, diphtheria, and pertussis in the United States” in order to provide clinicians and public health providers with a comprehensive and up-to-date “resource.”4 Id. at 3-4. This April 2018 publication reflects the ACIP’s recommendation that GBS occurring less than six weeks after receipt of a tetanus toxoid-containing vaccine warrants a precaution for subsequent administration of tetanus toxoid-containing vaccines. Id. at 6. Court Exhibit 1002,5 a 2019 ACIP publication which outlines the ACIP’s best practice guidelines for several vaccine-preventable diseases, likewise listed GBS less than six weeks after a previous dose of tetanus toxoid- containing vaccine as a precaution for the DT, Td, Tdap, and DTaP vaccinations. ECF 96- 2 at 53, 57. The Special Master directed the parties to share the Court Exhibits with their

4 Court Ex. 1001: Centers for Disease Control and Prevention, Prevention of Pertussis, Tetanus, and Diphtheria with Vaccines in the United States: Recommendations of the Advisory Committee on Immunization Practices (ACIP), 67 CDC MORBIDITY & MORTALITY WKLY. REP. 1 (Apr. 27, 2018), https://www.cdc.gov/mmwr/volumes/67/rr/pdfs/rr6702a1-H.pdf. 5 Court Ex. 1002: EZEANOLUE E, ET AL., General Best Practice Guidelines for Immunization: Best Practices Guidance of the Advisory Committee on Immunization Practices (2019).

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