Wright v. Fowler

991 S.W.2d 343, 1999 Tex. App. LEXIS 2640, 1999 WL 194196
CourtCourt of Appeals of Texas
DecidedApril 8, 1999
Docket2-98-070-CV
StatusPublished
Cited by24 cases

This text of 991 S.W.2d 343 (Wright v. Fowler) is published on Counsel Stack Legal Research, covering Court of Appeals of Texas primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Wright v. Fowler, 991 S.W.2d 343, 1999 Tex. App. LEXIS 2640, 1999 WL 194196 (Tex. Ct. App. 1999).

Opinion

OPINION

WILLIAM BRIGHAM, Justice.

This is an appeal from a summary judgment against Appellant, William R. Wright, in favor of Appellee, James H. Fowler, M.D. in a malpractice suit arising out of elective cosmetic surgery and procedures. Because the record establishes that Appellee conclusively proved Appellant’s medical negligence action was barred by the statute of limitations, and Appellant failed to plead a Deceptive Trade Practices (DTPA) cause of action that is not barred by the Medical Liability and Insurance Improvement Act (MLIIA), we affirm.

Facts

On December 4, 1989, Appellee placed silicone cheek implants in Appellant’s face. Before surgery, Appellant signed a surgical consent form that listed allergic reactions, infection, failure to achieve satisfactory cosmetic results, and numbness of cheek among the possible risks. On February 26, April 19, and June 7, 1990, Ap-pellee injected liquid silicone drops into several sites on Appellant’s face. On June 7, 1990, Appellant complained of pain and discomfort in his right upper cheek. On July 12, 1990, Appellee surgically repositioned one of the implants. Before that surgery, Appellant signed a similar consent form. Several months after the second surgery, Appellant requested-his medical records from Appellee because Appellant “knew [he would] never return to see [Appellee] again,” and was afraid Appellee wouldn’t keep them.

In 1993 or early 1994, Appellant saw an allergist because he was experiencing tiredness and malaise. He was treated for *347 allergic rhinitis with allergy shots and antihistamines on a regular basis for approximately two years.

On April 5, 1994, Appellant engaged another plastic surgeon, Dr. Steve Byrd, to remove the implants because his face had started hurting again. In June 1994, Appellant took a “rubbery” substance from his nose to his allergist for inspection. He told his allergist that Appellee had injected him with silicone, and asked whether the allergist thought it necessary to know what kind of silicone it was. The allergist advised Appellant that Dow Corning made all the injectable silicone.

In June 1994, Appellant sent a certified letter to Appellee discussing his concern about his health 1 and recent articles concerning silicone, and advising Appellee that the physician who removed his implants shared his “concern for possible future systemic problems.” Appellant also requested that Appellee identify the specific type of silicone he had injected into Appellant’s face. Appellee responded by letter in July 1994, informing Appellant that the silicone used was “medical grade silicone” manufactured by Dow Corning, and stating the volume of silicone injected into each site. Appellee’s response also included a package insert on Dow Corning “360 medical fluid.”

Appellant was examined on July 15,1994 by a staff doctor at the University of South Florida Medical School, and was told by Dr. Frank Vasey that he should exercise and take certain medications for his symptoms of fatigue. The clinical record from the visit reflects an assessment of silicone-related disorder. Some time after that, Appellant was treated for a sinus infection and he later had one visit with a rheuma-tologist.

Procedural History

In his original petition, filed on October 24, 1994, Appellant sued Appellee and several other defendants, 2 complaining of defective implants and silicone fluid, and invoking the doctrines of strict liability, breach of warranty, and negligence. On December 15, 1995, Appellant non-suited all defendants except Appellee, his professional association, and McGhan. 3

On September 26,1997, Appellee and his professional association moved for summary judgment on all causes of action, and the court set a hearing on the motion for October 17, 1997. On October 7, 1997, Appellant filed his first amended original petition, adding allegations that Appellee’s actions “further constitute medical malpractice and violations of the Deceptive Trade Practices Act....” Appellant’s response to Appellees’ motion for summary judgment was filed on October 9, 1997.

The following exhibits were attached to or referenced by Appellant’s response. The entire deposition of Appellant was attached as Exhibit A; the deposition of Appellee in a different cause of action brought by a different plaintiff against Ap-pellee was attached as Exhibit B. There was no exhibit C attached, but Appellant’s response stated that “the deposition of [Appellee] in this case is scheduled for October 16, 1997, after delays requested] by the defendant[;][i]t will be attached as Exhibit C.” Exhibit D consisted of medical records from Dr. Byrd. Exhibit E included Appellant’s medical records from the University of South Florida College of Medicine. Exhibit F was a copy of 1976 correspondence concerning the FDA’s rejection of Dow Coming’s application for approval *348 of the silicone fluid. Attached as Exhibits G and H were epidemiologic studies on silicone injections and implants. Finally, Exhibit I consisted of Appellant’s medical records from Dr. James Denton. 4

In his response, Appellant referenced an affidavit of Dr. John Barnett for the proposition that Appellee’s conduct fell below the standard of care. No affidavit of Dr. Barnett was attached. Appellant’s response alleged that he suffered not only a systemic injury, but also a local injury. 5 He further alleged that he “began suffering local and systemic problems in the latter part of 1998;” 6 that he “most likely ... discovered” that his cheek implants were silicone in 1994; 7 and that suit was filed “well within the ... discovery rule.”

By supplemental response dated October 10,1997, Appellant filed a deposition of Dr. Barnett, which was taken in a different cause of action out of district court in Dallas County styled Lori Murphy v. James H. Fowler. Appellant faxed excerpts of the deposition of Dr. Barnett to Appellee on October 10, 1997, and stated in a transmittal letter that Appellant was “attempting to obtain an Affidavit from Dr. John Barnett [but that] due to his inavailability, [sic] [Appellant] ha[s] been unable to obtain that affidavit timely.” On October 15, 1997, Appellant filed the affidavit, which states that in Dr. Barnett’s opinion, the facial injections of silicone liquid performed by Appellee constituted negligence and fell outside the bounds of accepted standard medical care. On October 14, 1997, Appellant faxed the affidavit to Appellee.

On October. 17, 1997, the trial court granted “partial summary judgment on all grounds stated” in Appellee’s motion for summary judgment. An order to that effect was signed on October 24,1997.

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991 S.W.2d 343, 1999 Tex. App. LEXIS 2640, 1999 WL 194196, Counsel Stack Legal Research, https://law.counselstack.com/opinion/wright-v-fowler-texapp-1999.