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  "name": "Lewis EADY v. Bryan K. LANSFORD",
  "name_abbreviation": "Eady v. Lansford",
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    "judges": [],
    "parties": [
      "Lewis EADY v. Bryan K. LANSFORD"
    ],
    "opinions": [
      {
        "text": "Tom Glaze, Justice.\nIn this case, Lewis Eady challenges the constitutionality of the Arkansas Medical Malpractice Act, codified at Ark. Code Ann. \u00a7\u00a7 16-114-201, et seq. (1987 and Supp. 2001), with respect to cases involving informed consent. The trial court rejected Eady\u2019s argument. Specifically, Eady argues that Ark. Code Ann. \u00a7 16-114-206(b) (1987 and Supp. 2001) is invalid as special legislation under Ark. Const, amend. 14, and violates his equal protection rights under U.S. Const, amend. 14 and Ark. Const, art. 2, \u00a7 3. Alternatively, if\u00a7 16 \u2014 114\u2014206(b) is constitutional, Eady submits that our court should apply the \u201ccommon knowledge\u201d exception to informed consent cases.\nThe facts leading to this controversy can be briefly stated. Eady saw Dr. Bryan Lansford about complaints Eady had of seasonal allergy symptoms, nasal congestion, and facial pain. Dr. Lansford diagnosed Eady as having allergic rhinitis and possible sinusitis. The doctor ordered an allergy evaluation, a CT scan of Eady\u2019s sinuses, and nasal steroids, and he gave Eady a prescription for Bactrim and asked him to return in two weeks. Upon Eady\u2019s return, the doctor noted that Eady suffered from allergies and suggested Eady might want to consider endoscopic sinus surgery.\nEady continued to feel bad, and, because he could not get in to see Dr. Lansford right away, Eady went to a medical clinic where he was examined, prescribed an antibiotic, and given an analgesic. Two days later, the clinic also gave Eady a prescription for Lorabid and Darvocet for pain. Later that same day, Eady went to the hospital because he could not eat or drink anything, and he began to spit up blood. At the hospital, Eady was diagnosed with Stevens-Johnson Syndrome, an allergic reaction to the Bactrim prescribed by Dr. Lansford. Eady\u2019s skin began to peel, he lost his vision, and suffered from other symptoms, including the sloughing of the lining of his esophagus and stomach. He remained in the hospital for twenty-five days and suffered numerous residual effects, including impaired vision and darkened skin.\nEady filed suit against Dr. Lansford, alleging the doctor committed medical malpractice and had been negligent, among other things, by failing to warn Eady of the possible side effects of Bactrim, including Stevens-Johnson Syndrome. He also alleged the doctor failed to obtain Eady\u2019s informed consent before prescribing Bactrim. Dr. Lansford responded by moving for summary judgment, attaching an affidavit by Dr. Ehab Hanna, an expert in otolaryngology; Dr. Hanna opined that Lansford\u2019s treatment did not fall below the standard of care for an ENT (ear, nose, and throat) specialist in Fort Smith. Eady responded by submitting that \u00a7 16-14-206 (b) is unconstitutional as special legislation and as violative of the equal protection clause; he further contended summary judgment was inappropriate because there were genuine factual issues to be decided by a jury. Eady did not submit any medical expert affidavit or testimony to counter that furnished by Dr. Hanna.\nThe trial court rejected Eady\u2019s constitutional arguments, stating that Arkansas law is well-settled that expert witnesses are required if the alleged medical negligence is outside a jury\u2019s comprehension and not a matter of \u201ccommon knowledge.\u201d Thus, because Eady did not respond to Dr. Lansford\u2019s summary judgment motion with any expert testimony of his own, the trial court ruled that Dr. Lansford was entitled to summary judgment.\nOn appeal, Eady contends that \u00a7 16-114-206(b) is out of step with modern medical practices. With respect to cases where a patient\u2019s informed consent is at issue, that statute provides as follows:\n(b)(1) Without limiting the applicability of subsection (a) of this section, where the plaintiff claims that a medical care provider failed to supply adequate information to obtain the informed consent of the injured person, the plaintiff shall have the burden of proving that the treatment, procedure, or surgery was performed in other than an emergency situation and that the medical care provider did not supply that type of information regarding the treatment, procedure, or surgery as would customarily have been given to a patient in the position of the injured person or other persons authorized to give consent for such a patient by other medical care providers with similar training and experience at the time of the treatment, procedure, or surgery in the locality in which the medical care provider practices or in a similar locality.\n(2) In determining whether the plaintiff has satisfied the requirements of subdivision (b)(1) of this section, the following matters shall also be considered as material issues:\n(A) Whether a person of ordinary intelligence and awareness in a position similar to that of the injured person or persons giving consent on his behalf could reasonably be expected to know of the risks or hazards inherent in such treatment, procedure, or surgery;\n(B) Whether the injured party or the person giving consent on his behalf knew of the risks or hazard inherent in such treatment, procedure, or surgery;\n(C) Whether the injured party would have undergone the treatment, procedure, or surgery regardless of the risk involved or whether he did not wish to be informed thereof;\n(D) Whether it was reasonable for the medical care provider to limit disclosure of information because such disclosure could be expected to adversely and substantially affect the injured person\u2019s condition.\n\u00a7 16-114-206(b).\nAs is readily seen by reading \u00a7 16-114-206, the burden is on the plaintiff to prove that the physician failed to supply the type of adequate information regarding the treatment or procedures as would have been given by physicians in the same, or in a similar, locality. In Fuller v. Starnes, 268 Ark. 476, 597 S.W.2d 88 (1980), this court discussed in some depth the divergent views of American courts concerning the degree of disclosure necessary to render a consent adequate and informed so as to bind the patient:\nAlthough the existence of a physician\u2019s duty to warn a patient of hazards of future medical treatment is generally recognized, a wide divergence of views has developed concerning the appropriate standard for measuring the scope of the duty. The minority view is that the duty of a physician to disclose is measured by the patient\u2019s need for information material to the patient\u2019s right to decide whether to accept or reject the proposed medical treatment. Emphasizing the right of the patient to control what happens to his body, the minority view is undergirded by the proposition that what a patient should be told about future medical treatment is primarily a human judgment. The majority view is that the duty of a physician to disclose is measured by the customary disclosure practices of physicians in the community or in a similar community. This view emphasizes the interest of the medical profession to be relatively free from vexatious and costly litigation and holds that what a patient should be told about future medical treatment is primarily a medical decision.\nFuller, 268 Ark. at 478 (citations omitted) (emphasis added). See also Grice v. Atkinson, 308 Ark. 637, 826 S.W.2d 810 (1992) (where court continued to adhere to the Fuller case, stating that this court chose the majority view, which places on the plaintiff the burden of proving that the physician failed to supply the type of adequate information regarding the surgery as would have been given by other physicians in the same, or in a similar, locality); Aronson v. Harriman, 321 Ark. 359, 901 S.W.2d 832 (1995); Brumley v. Naples, 320 Ark. 310, 896 S.W.2d 860 (1995).\nEady cites to and quotes from a New Jersey Supreme Court decision, Perez v. Wyeth Lab., Inc., 734 A.2d 1245, 1246-47 (N.J. 1999), which contains broad policy language that seems to justify medical product cases directly against drug manufacturers, but Eady fails to clarify how such a policy suggests the obsolescence or unconstitutionality of \u00a7 16-114-206(b). In fact, Eady\u2019s argument explicitly recognizes that Arkansas \u201cstill clings to\u201d the majority view established in Fuller.\nWhile our court and the Arkansas General Assembly have adopted the majority view that the duty of a physician to disclose is measured by the customary practices of physicians in the community or in a similar community, Eady still maintains that it is unconstitutional for \u00a7 16-114-206(b) to require a medical expert in every case involving informed consent and that it grants a privilege to health care providers that is not granted to other professionals; he argues that there is no rational basis for drawing a distinction between informed consent cases and other medical malpractice cases.\nOf course, there is a presumption of validity attending every consideration of a statute\u2019s constitutionality; every act carries a strong presumption of constitutionality, and before an act will be held unconstitutional, the incompatibility between it and the constitution must be clear. Gay v. Rabon, 280 Ark. 5, 652 S.W.2d 836 (1983). Any doubt as to the constitutionality of a statute must be resolved in favor of its constitutionality. Id. The heavy burden of demonstrating the unconstitutionality of a statute is upon the one attacking it. Id.\nHere, in order to prove that the requirement of expert testimony in informed consent cases violates the equal protection clause, Eady would have to demonstrate that there is no rational basis for such a requirement. See Raley v. Wagner, 346 Ark. 234, 57 S.W.3d 683 (2001) (finding rational basis for two-year statute of limitations in medical malpractice cases). Under the rational basis test, legislation is presumed constitutional and rationally related to achieving any legitimate governmental objective under any reasonably conceivable fact situation. Fayetteville Sch. Dist. v. Arkansas State Bd. of Educ., 313 Ark. 1, 852 S.W.2d 122 (1993). This presumption places the burden of proof on the party challenging the legislation to prove its unconstitutionality. Id.\nThe test is the same for cases in which it is alleged that a statute is unconstitutional special legislation. Id. Legislation is special \u201cif by some inherent limitation or classification it arbitrarily separates some person, place, or thing from those upon which, but for such separation, it would operate [.]\u201d Id. (citing Owen v. Dalton, 296 Ark. 351, 757 S.W.2d 921 (1988) (emphasis supplied in text). The determinative factor is whether the General Assembly acted in an arbitrary manner to separate one class of persons from another, and we apply the rational basis test to determine whether such a separation is arbitrary. Id. (citing Streight v. Ragland, 280 Ark. 206, 655 S.W.2d 459 (1983)).\nEady has offered no proof that the General Assembly acted arbitrarily, or that the legislation is not rationally related to achieving any legitimate objective of the government under any reasonably conceivable fact situation, beyond a bare assertion that \u201cthe statute\u2019s goals of reducing medical costs and malpractice premiums would not be achieved through the imposition of the professional standard with regard to informed consent cases.\u201d Clearly, there is a rational relationship between the burden of proof required and the achievement of a legitimate governmental objective. The emergency clause of the Medical Malpractice Act states as follows:\nIt is hereby found, determined and declared by the General Assembly that the threat of legal actions for medical injury have resulted in increased rates for malpractice insurance which in turn causes and contributes to an increase in health care costs placing a heavy burden on those who can least afford such increases and that the threat of such .actions contributes to expensive medical procedures to be performed by physicians and others which otherwise would not be considered necessaryf,] and that this Act should be given effect immediately to help control the spiraling cost of health care.\nIt is made clear by the General Assembly that the objective of the Act is to control rapidly increasing health care costs. The requirement of producing expert testimony in informed consent cases assists in keeping such costs down; in the absence of such a requirement, nearly every informed consent claim would create a jury question as to whether the \u201cprudent patient\u201d standard (i.e., the minority standard) had been met. This would result in more litigation, higher costs, and greater expenses to the medical profession, which would in turn be passed on to patients and health care consumers. Thus, the General Assembly did not act arbitrarily in requiring a different degree of proof in informed consent cases than in other medical malpractice cases.\nFinally, Eady argues that, in the event the court determines that the act is constitutional, we should alternatively apply the \u201ccommon knowledge\u201d exception to informed consent cases. This exception provides that expert medical testimony is not required when the asserted negligence lies within the comprehension of a jury of laymen, such as a surgeon\u2019s failure to sterilize his instruments or to remove a sponge from the incision before closing it. See Haase v. Starnes, 323 Ark. 263, 915 S.W.2d 675 (1996) (citing Lanier v. Trammel, 207 Ark. 372, 180 S.W.2d 818 (1944)). On the other hand, when the applicable standard of care is not a matter of common knowledge, the jury must have the assistance of expert witnesses in coming to a conclusion upon the issue of negligence. Id.\nEady argues that this \u201ccommon knowledge\u201d exception should apply \u201cbecause a prudent patient would want to know about serious risks of death or severe injury from a treatment.\u201d Flere, the asserted negligence was Dr. Lansford\u2019s alleged failure to inform Eady of the potential for developing Stevens-Johnson syndrome. The question is whether this asserted negligence lies within the comprehension of a jury of laymen. Eady asserts that it does, because the jury could understand that a reasonably prudent patient in his position would have opted for a different treatment, had he been informed of the possibility of suffering this serious complication, and he argues that the \u201ccommon knowledge\u201d exception should apply to informed consent cases, because \u201ca lay jury can understand that a physician has a duty to disclose potential side effects which may cause death or a significant risk of death.\u201d\nHowever, such argument simply ignores the requirement in \u00a7 16-114 \u2014 206(b) that an informed-consent plaintiff must demonstrate \u201cthat the medical care provider did not supply the type of information ... as would customarily have been given to a patient in the position of the injured person ... by other medical care providers with similar training and experience at the time of the treatment ... in the locality in which the medical care provider practices or in a similar locality.\u201d To accept Eady\u2019s argument would require holding \u00a7 16-114-206(b) unconstitutional. One cannot \u201calternatively\u201d apply the common knowledge exception to informed consent cases without striking \u00a7 16-114-206(b) in its entirety. As discussed above, we hold the statute is constitutional, and therefore, the court will not \u201calternatively\u201d apply the comr mon knowledge doctrine.\nIn sum, Dr. Lansford presented expert testimony to the effect that he was acting within the required standard of care of physicians engaged in the practice of otolaryngology during 1996 within the State of Arkansas. Dr. Lansford\u2019s expert stated that the prescribing of Bactrim was appropriate for the treatment of Eady\u2019s symptoms, and that, although a physician does have a duty to inform a patient about commonly encountered side effects, the risk of developing Stevens-Johnson syndrome is so rare that doctors do not specifically advise of that risk unless a patient has a known allergy to sulfonamides such as Bactrim. Further, Dr. Lansford\u2019s expert pointed out that Eady\u2019s condition was about the same on September 25, 1996, as it had been on September 13, 1996, and there was no reason presented to Dr. Lansford to have discontinued Eady\u2019s taking of Bactrim at that time.\nRather than meeting proof with proof, and offering expert testimony of his own, Eady chose to challenge the constitutionality of the statute. The proof required to survive a motion for summary judgment in a medical malpractice case must be in the form of expert testimony. Ford v. St. Paul Fire & Marine Ins. Co., 339 Ark. 434, 55 S.W.3d 460 (1999) (citing Oglesby v. Baptist Medical System, 319 Ark. 280, 891 S.W.2d 48 (1995)). Eady offered no proof whatsoever to demonstrate that Dr. Lansford violated the appropriate standard of care. Because Eady failed to meet proof with proof in the form of expert testimony, the trial court did not err in granting Dr. Lansford\u2019s motion for summary judgment, and the lower court\u2019s decision is therefore affirmed.",
        "type": "majority",
        "author": "Tom Glaze, Justice."
      }
    ],
    "attorneys": [
      "Law Offices of Charles Karr, P.A., by: Charles Karr and Shane Roughley, for appellant.",
      "Warner, Smith & Harris, PLC, by: Waynr Harris, for appellee."
    ],
    "corrections": "",
    "head_matter": "Lewis EADY v. Bryan K. LANSFORD\n02-695\n92 S.W.3d 57\nSupreme Court of Arkansas\nOpinion delivered December 12, 2002\nLaw Offices of Charles Karr, P.A., by: Charles Karr and Shane Roughley, for appellant.\nWarner, Smith & Harris, PLC, by: Waynr Harris, for appellee."
  },
  "file_name": "0249-01",
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  "last_page_order": 285
}
