Doe v. Johnston

476 N.W.2d 28, 1991 Iowa Sup. LEXIS 344, 1991 WL 181901
CourtSupreme Court of Iowa
DecidedSeptember 18, 1991
Docket90-448
StatusPublished
Cited by23 cases

This text of 476 N.W.2d 28 (Doe v. Johnston) is published on Counsel Stack Legal Research, covering Supreme Court of Iowa primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Doe v. Johnston, 476 N.W.2d 28, 1991 Iowa Sup. LEXIS 344, 1991 WL 181901 (iowa 1991).

Opinion

NEUMAN, Justice.

This medical malpractice case concerns the scope and adequacy of informed consent secured from a surgery patient who developed transfusion-associated acquired immunodeficiency syndrome (AIDS). A jury returned a verdict in favor of the surgeon and this appeal followed. We affirm.

The operative facts are largely undisputed. In February 1985 defendant Richard Johnston — an orthopedic surgeon — performed a total hip replacement on a fifty-year-old patient identified in these proceedings as John Doe. The procedure was successful and no allegations of negligence are made about the surgery itself. As part of his postoperative recovery, however, Doe received a blood transfusion ordered by Dr. Johnston. Two years later, in February 1987, Doe learned that the donor of the transfused blood carried the human immunodeficiency virus (HIV). Subsequent tests revealed that Doe had acquired the dread disease AIDS.

Doe and his wife brought this action against Iowa Methodist Medical Center, The Blood Center of Central Iowa, and Dr. Johnston. The hospital and blood bank ultimately settled with the plaintiffs, and trial proceeded solely against the doctor. The controversy centered on whether the transfusion ordered by Dr. Johnston was medically necessary, and whether the doctor breached the standard of medical care by failing to warn Doe of the risk of acquiring AIDS through a blood transfusion or, in the alternative, failing to advise him of the possibility of self-donating the necessary units of blood. This latter procedure is known as an autologous transfusion.

Exceptionally well-qualified witnesses from across the country offered their expert opinions on these issues, pro and con. The jury listened to fifteen days of testimony from specialists in epidemiology, pathology, hematology, and orthopedic surgery. It ultimately rendered its verdict finding Dr. Johnston without fault.

On appeal from the judgment entered upon the jury’s verdict, the plaintiffs raise six issues. Two relate to the issue of informed consent: the propriety of the court’s refusal to direct a verdict in plaintiffs’ favor, and its unwillingness to instruct on the feasibility of autologous transfusion; two evidentiary issues pertain to admissibility of surgery photos and interrogatory answers about remedial measures taken by the physician; and two concern alleged juror misconduct. We shall consider these matters in turn.

I. Informed Consent.

A. The record contains no dispute over the fact that when Dr. Johnston advised Doe about the risks associated with hip replacement surgery he made no mention of the risk of contracting AIDS from a blood transfusion. Nor did he advise Doe that the risk could be avoided altogether through the use of an autologous transfusion. Thus, the question posed to the trial court — and renewed on appeal — is whether, in February 1985, the risk of contracting AIDS from blood products was so material, and the use of autologous transfusion so reasonable, that the doctor was negligent as a matter of law in failing to so advise his patient. The trial court rejected plaintiffs’ suggestion that the evidence com *31 pelled a directed verdict in favor of the plaintiffs, and submitted the question to the jury. It is from this decision, and the court’s refusal to enter judgment notwithstanding the verdict, that plaintiffs now appeal.

At the outset we note the familiar rule that only in the “exceptional case” should a district court direct a verdict in favor of either party on a negligence claim. Iowa R.App.P. 14(f)(10). The party opposing the motion is entitled to the benefit of every legitimate inference which may be drawn from the evidence, and if reasonable minds might differ on the issue, a jury question is generated. Pauscher v. Iowa Methodist Medical Center, 408 N.W.2d 355, 361 (Iowa 1987); Rippel v. J.H.M. of Waterloo, Inc., 328 N.W.2d 499, 500 (Iowa 1983). Moreover, Doe bore the burden of proving negligence and “[o]nly rarely may a verdict be directed in favor of one who has the burden of proof.” McCaull v. Universal Mfg. Co., 218 N.W.2d 592, 593 (Iowa 1974).

Mindful of this standard, Doe argues forcefully that this is the exceptional case. He points to the fact that every physician testifying acknowledged autologous transfusion as the safest form of blood transfusion even prior to 1985, and that it had been a known and available alternative to homologous (anonymous donor) transfusion for many years. And even though defendant’s experts testified that it was not a breach of the standard of care to fail to inform of the risk of AIDS or the alternative of autologous transfusion in 1985, each admitted it was a reasonable and responsible practice which several of them included in their preoperative procedures at that time.

The issue boils down to application of the “patient rule.” Under the rule, the patient’s right to make an informed decision about submitting to a particular medical procedure places a duty on the doctor to disclose all material risks involved in the procedure. Pauscher, 408 N.W.2d at 358; Cowman v. Hornaday, 329 N.W.2d 422, 425-26 (Iowa 1983). That duty is shaped, not by what the medical community would deem material, but by the patient’s need for information sufficient to make a truly informed and intelligent decision. Pauscher, 408 N.W.2d at 359. This is a decision uniquely within the realm of a lay jury. Id. at 360.

To prove a breach of this standard, the burden rests with the plaintiff to establish by expert testimony the nature of the risk involved and the likelihood of its occurrence. Id. It is then for the jury to decide, “from the standpoint of the reasonable patient, whether the risk is in fact a material one.” Id. (emphasis added).

The record before us reveals agreement among the experts that in 1985 prudence dictated discussion of AIDS in the blood supply because of the publicity about it in both lay and professional journals. There was considerable conflict in the evidence, however, regarding the experts’ perception of the actual risk of contracting HIV through donated blood. Dr. Johnston assessed the risk in 1985 at one in 250,000. He thought this too remote a consequence of otherwise beneficial surgery to unnecessarily alarm his patients. His experts, who were all leaders in the field of orthopedic surgery, likewise placed the risk in the range of one in 100,000 to one in a million. By contrast, plaintiffs’ experts in epidemiology and pathology assessed the risk much higher and were critical of Dr. Johnston’s failure to broách the topic with his patient. Clearly, however, the evidence of materiality was in conflict, and the court properly submitted the issue to the jury.

The doctor’s failure to offer Doe the alternative of an autologous transfusion poses a separate question. As defined in Cowman and Pauscher,

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Cite This Page — Counsel Stack

Bluebook (online)
476 N.W.2d 28, 1991 Iowa Sup. LEXIS 344, 1991 WL 181901, Counsel Stack Legal Research, https://law.counselstack.com/opinion/doe-v-johnston-iowa-1991.