Fu v. Unc Chapel Hill

CourtNorth Carolina Industrial Commission
DecidedFebruary 12, 2007
DocketNo. 439227.
StatusPublished

This text of Fu v. Unc Chapel Hill (Fu v. Unc Chapel Hill) is published on Counsel Stack Legal Research, covering North Carolina Industrial Commission primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Fu v. Unc Chapel Hill, (N.C. Super. Ct. 2007).

Opinion

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The undersigned have reviewed the prior Opinion and Award based upon the record of the proceedings before Deputy Commissioner Donovan and the briefs and arguments of the parties. The appealing party has shown good ground to reconsider the evidence. Accordingly, the Full Commission reverses the Opinion and Award of the Deputy Commissioner and enters the following Opinion and Award.

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The Full Commission finds as fact and concludes as matters of law the following, which were entered into by the parties at the hearing before the Deputy Commissioner as:

STIPULATIONS
1. Plaintiff contends that she sustained a compensable injury by accident or an occupational disease by inoculation on March 9, 2004. *Page 2

2. At the time of the injury which is the subject of this claim, the parties were subject to and bound by the provisions of the North Carolina Workers' Compensation Act.

3. At all times relevant to this claim, the employer-employee relationship existed between plaintiff and defendant-employer.

4. Key Risk Management Services, Inc., is the administrator of the claim.

5. Plaintiff's average weekly wage as of the date of her injury was $935.17, yielding a compensation rate of $623.48 per week.

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Based upon all of the competent evidence of record and reasonable inferences flowing therefrom, the Full Commission makes the following:

FINDINGS OF FACT
1. At the time of the hearing before the Deputy Commissioner, plaintiff was 53 years old. Plaintiff is medical doctor and a native of China who was employed there doing investigative work regarding the pathology of the HIV virus. Her work came to the attention of American researchers who invited plaintiff to participate in HIV research at the University of North Carolina in Chapel Hill (hereinafter, UNC).

2. Plaintiff began working in the Gene Therapy Center at UNC where for approximately four years she did research and performed clinical trials. Thereafter, she spent approximately two years as a Research Analyst I in the Department of Microbiology and Immunology.

3. In order to investigate the HIV virus, researchers use the Venezuelan Equine Encephalitis virus (hereinafter, VEE), as it has physical properties similar to those of HIV and there exists a vaccination for VEE. As a prerequisite to her employment, plaintiff was required *Page 3 to receive the VEE vaccination so that she could enter the laboratory in which the live VEE virus was housed.

4. The U.S. Military is in the process of testing the VEE virus vaccine on humans. The vaccine is in the experimental stages and is approved for use on human beings for research purposes only. Currently, the vaccine is in Phase II testing for safety and immunogenicity, which measures the development of antibodies in response to the vaccine.

5. Prior to working in the lab, plaintiff was required to undergo tests, including a hematology with complete blood count (cbc) and a differential platelet count, a normal biochemistry evaluation with electrolytes and liver function studies. In addition, a research analyst was required to have a normal negative HIV titer and a negative hepatitis C test. Finally, it was mandated that each participant undergo a urinalysis, EKG and a chest x-ray. Each research analyst was screened for VEE antibody titers to insure that he or she had not been exposed to the VEE virus in the past or that he or she has not previously received a vaccination.

6. Once a person receives the initial vaccination containing live VEE virus, the person's blood is evaluated for the presence of antibodies to the virus. If the antibody level is sufficiently high, no booster shot is required. If the antibody level is too low, a second inoculation is required. The vaccine used in the booster shot is supposed to be killed by formulin, but at least one study shows that humans may still become infected with the virus following a booster shot. The virus most often causes flu-like symptoms, but can cause serious illness or death in humans.

7. The results of plaintiff's tests did not reveal anything unusual. In addition, plaintiff tested negative for the VEE titer indicating that she had not previously been exposed to the VEE virus. *Page 4

8. On September 16, 2003, plaintiff received the first of two scheduled vaccinations containing the live VEE virus at the U.S. Army Medical Research Institute of Infectious Disease (USAMRIID) at Fort Detrick, Maryland. Prior to receiving the vaccination, plaintiff had no history of infections or viral illness and was in good health.

9. Within two days of receiving the initial vaccine, plaintiff began to experience symptoms, including nausea, fever, headaches, fatigue and myalgia. The symptoms resolved within six days.

10. Plaintiff's titer level did not change following the first inoculation, indicating that her body had not mounted an immunological response to the vaccine. Accordingly, she was required to receive the booster shot. Plaintiff received the booster on March 9, 2004.

11. The day following the second inoculation, plaintiff immediately began to experience side effects similar to those which followed the first vaccine; however, the symptoms did not resolve. Plaintiff kept a detailed chart of her symptoms, including faintness, difficulty with balance and walking, fever, headache, rapid pulse, heart palpitations, muscle aches, cough, sore throat, runny nose, chills, diarrhea, shortness of breath and general weakness. Plaintiff's symptoms continued through September 2004.

12. Dr. Ellen Boudreau, chief of the USAMRIID special immunizations program, testified regarding plaintiff's participation in the program. Dr. Boudreau stated that approximately two thirds of those receiving the live virus vaccine experience side effects similar to those plaintiff experienced following the first inoculation and for a like period of time.

13. Regarding the second inoculation, Dr. Boudreau opined that testing on plaintiff on March 23, 2004 showed that her post-inoculation white blood cell count was about the same as her pre-inoculation count, indicating that there was no acute infection. She further noted that *Page 5 there is only 15% to 17% incidence of side effects from the second type of vaccine, but usually the side effects are not as pronounced or prolonged.

14. After the onset of side effects following the second inoculation, plaintiff initially treated at UNC hospital where she was diagnosed with a viral upper respiratory tract infection. After her symptoms persisted for a period of time, plaintiff contacted Dr. Boudreau and was referred by her employer to the care of Dr. Robert Gwyther, a board-certified specialist in family medicine.

15. On April 16, 2004, plaintiff presented to Dr. Gwyther with complaints of myalgias, chills, headache, and nausea, which had been present since she received the booster shot for VEE in March 2004. Dr. Gwyther attributed plaintiff's condition as a reaction to the vaccine. Dr. Gwyther ordered a number of tests, recommended rest for plaintiff and wrote her out of work for one week.

16. Plaintiff returned to Dr. Gwyther on May 3, 2004. Her symptoms had improved somewhat. Plaintiff's tests had come back normal and Dr. Gwyther opined that the symptoms resulting from the VEE vaccine were tapering off. After consultation with Dr.

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Fu v. Unc Chapel Hill, Counsel Stack Legal Research, https://law.counselstack.com/opinion/fu-v-unc-chapel-hill-ncworkcompcom-2007.