Grant v. Secretary of Health and Human Services

United States Court of Federal Claims·Decided December 4, 2019·No. 17-1816·Unpublished

Opinion

In the United States Court of Federal Claims OFFICE OF SPECIAL MASTERS Filed: October 29, 2019

* * * * * * * * * * * * * INDIGO GRANT, * Parent and natural guardian of * UNPUBLISHED M.G., a minor, * * No. 17-1816V Petitioner, * v. * Special Master Gowen * SECRETARY OF HEALTH * Attorneys’ Fees and Costs; Reasonable AND HUMAN SERVICES, * Basis; Interim Award; Motion to Withdraw; * Intra-Office Communications; Duplicative Respondent. * Work. * * * * * * * * * * * * *

Renee J. Gentry, Vaccine Injury Clinic, George Washington University Law School, Washington, DC, for petitioner. Adriana R. Teitel, United States Department of Justice, Washington, DC, for respondent.

DECISION ON INTERIM ATTORNEYS’ FEES AND COSTS1

On November 20, 2017, Indigo Grant, as parent and natural guardian of M.G., a minor (“petitioner”), filed a petition for compensation in the National Vaccine Injury Compensation Program. Petitioner’s claim relates to M.G.’s receipt of diptheria-tetanus-acellular pertussis (“DTaP”), Haemophilus influenzae type B (“Hib”), and inactivated polio virus (“IPV”) vaccines on December 30, 2014, as well as DTaP, Hib, IPV, and Pneumococcal vaccines on February 26, 2015. Petitioner alleges that as a result of these vaccines, M.G. suffered sepsis, severe dermal reactions, and eventually death on January 13, 2016. Petitioner’s counsel now requests an award of interim attorneys’ fees and costs upon seeking to withdraw from the claim. I hereby GRANT petitioner’s motion and award $21,604.90 in interim attorneys’ fees and costs.

1 Pursuant to the E-Government Act of 2002, see 44 U.S.C. § 3501 note (2012), because this opinion contains a reasoned explanation for the action in this case, I intend to post it on the website of the United States Court of Federal Claims. The court’s website is at http://www.uscfc.uscourts.gov/aggregator/sources/7. Before the opinion is posted on the court’s website, each party has 14 days to file a motion requesting 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). An objecting party must provide the court with a proposed redacted version of the opinion. Id. If neither party files a motion for redaction within 14 days, the opinion will be posted on the court’s website without any changes. Id. I. Summary of Relevant Facts

M.G. was born on October 25, 2014. Her family resided in Duchess County, New York. They established primary care with a pediatrician in that region. On November 8, 2014, she had a normal two-week exam. Ex. 2 at 33-34. On November 25, 2014, she had a normal one-month exam and received her second Hepatitis B vaccine. Id. at 2, 30-32. On December 30, 2014, M.G. had her two-month well-baby vaccination. She received DTaP, Hib, and IPV vaccinations in her left thigh. Id. at 2, 27-29.

Fourteen days after vaccination, on January 13, 2015, M.G.’s right cheek appeared pink, dry, and scaly. Ex. 3 at 1-2 (date-stamped photographs).

Thirty-eight days after vaccination, on February 7, 2015, M.G. was admitted to Inova Fairfax Hospital in Fairfax, Virginia. The medical records provide that the family was visiting from New York “for a couple weeks.” Ex. 5 at 5. M.G.’s brother, who was 14 months old, had a history of “recurrent highly resistant MRSA2 infections since the age of 1 month old, requiring 4 hospializations over the last year.” Id. He was recently discharged from Virginia Commonwealth University (“VCU”) Medical Center with diagnoses of Wiskott-Aldrich syndrome3 and hyper-IgE syndrome.4 Id. Petitioner was concerned that M.G. had developed a similar rash. Id. The emergency room attending physician recorded petitioner’s report that M.G. was “well until about 24 hours prior to presentation. Since then, [petitioner] noted skin changes on left leg, both arms, and scalp. Extremity wounds expanded, then the left leg and right arm opened and started to drain this evening. Patient has a history of cradle’s cap,5 but the flakiness had worsened and changed color from white to yellow.” Id. at 7. The admitting pediatrician recorded that petitioner “first noted dry skin 1 month ago (after using a particular detergent, however it persisted) but did not take pt to doctor as they’d moved and were in between PCPs. [Petitioner] has tried all kinds of emollients w/ little change.” Id. at 24. M.G.’s bloodwork was normal except for an elevated platelet count of 684 and elevated eosinophils at 1.24 (the reference ranges are not provided). Id. at 27. A wound culture and gram stain were positive for

2 MRSA is Staphylococcus aureus bacteria which is resistant to methicillin (a synthetic form of penicillin). Dorland’s Illustrated Medical Dictionary 32nd Ed. (2012) (hereinafter “Dorland’s”) at 1147, 1184, 1765.

3 Wiskott-Aldrich syndrome is “an X-linked immunodeficiency syndrome characterized by eczema, thrombocytopenia, and recurrent pyogenic infection. Patients cannot produce antibodies to polysaccharide antigens and have increased susceptibility to infection with encapsulated bacteria (Haemophilus influenzae, meningococcus, pneumococcus). Typically IgM is low, IgA and IgE are elevated, and there is anergy of the skin. Many affected persons also have lymphoreticular disorders.” Dorland’s at 1854.

4 Hyper-IgE syndrome is “a primary immunodeficiency disorder caused by mutations of the STAT3 gene. It is usually of autosomal dominant inheritance but sometimes occurs sporadically and is characterized by recurrent staphylococcal abscesses of skin, lungs, joints, and other sites; pruritic dermatitis; distinctive course facies; retained primary dentition; pruritic dermatitis; distinctive coarse facies; retained primary dentition; skeletal abnormalities; eosinophilia; and very high serum immunoglobulin E (IgE) levels.” Dorland’s at 1834.

5 Cradle cap is crusta lactea, a seborrhea (either excessive secretion of sebum, or dermatitis) of the scalp of nursing infants. Dorland’s at 282, 437, 1684.

2 staphylococcus and serratia odorifera. Id. at 49-50. Vancomycin6 was started then discontinued “as re-exam did not demonstrate any signs of infection.” Id. at 40. On February 8, 2015, M.G. was discharged from the hospital with an assessment of “diffuse severe eczema without evidence of bacterial superinfection.” IgE and multiple culture studies were pending. M.G. was to follow up with a pediatric allergist-immunologist and a pediatric dermatologist. Id. at 40-45.

On February 23, 2015, M.G. was readmitted to Inova Fairfax Hospital for worsened eczema, diarrhea, and fever. Ex. 5 at 115. During this hospitalization, M.G. received skin care and antibiotics. Id. at 115-17. On consultation, pediatric dermatologist Dr. Robert Silverman assessed: “The family history, past history of infections, and current diarrhea may be indicative of an immunodeficiency as a cause of this child’s dermatitis.” Dr. Silverman suggested further “immune workup.” Id. at 132. By February 25, 2015, M.G.’s skin was “improved” and she remained “afebrile and well-appearing.” The discharge plan was to follow up with her primary care provider as well as the pediatric allergist-immunologist and a pediatric dermatologist mentioned above. Petitioner objected to M.G.’s discharge and requested a second opinion. She was concerned that M.G. had an undiagnosed bacterial infection. Several physicians at the hospital were of the opinion that M.G.’s “exam and workup [we]re not consistent with a bacterial infection.” M.G. was referred to an immunologist at Children’s National Medical Center (“CNMC”) in Washington, DC. Id. at 151-52.

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