Spencer v. Goodill

17 A.3d 552, 2011 Del. LEXIS 179, 2011 WL 1312273
CourtSupreme Court of Delaware
DecidedApril 6, 2011
Docket411, 2010
StatusPublished
Cited by14 cases

This text of 17 A.3d 552 (Spencer v. Goodill) is published on Counsel Stack Legal Research, covering Supreme Court of Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Spencer v. Goodill, 17 A.3d 552, 2011 Del. LEXIS 179, 2011 WL 1312273 (Del. 2011).

Opinion

BERGER, Justice:

In this appeal, we consider the extent to which a plaintiff must prove causation to succeed in a medical negligence action based on lack of informed consent. Delaware’s informed consent statute codifies a health care provider’s duty to provide a patient with certain information about the alternatives and risks of a proposed treatment. A health care provider breaches that duty if it fails to provide information that would be material to the patient’s decision to undergo the proposed treatment. If the treatment is not successful, and the complication is one that should have been but was not disclosed, the patient has suffered damages. The question is whether the patient must prove not only that the complication was a material, undisclosed risk of the treatment, but also that a reasonable person, if told about the risk, would have declined the treatment. We conclude that proof of what a reasonable person would have done is required to establish causation. Accordingly, we affirm.

Factual and Procedural Background

In July 2007, Dr. John Goodill performed a bronchoscopy with a transbron-chial biopsy on Muriel Stewart. Goodill did not recall exactly what he told Stewart about the risks of the procedure. Based on his usual practice, however, he testified that he would have described the likely complications as bleeding, pneumothorax, and, at worst, use of a ventilator for a short period of time. Stewart was not informed that there was a one in 1000 risk of death, which is a magnitude of risk 500 times greater than the risk of death from general anesthesia. Unfortunately, Stewart died as a result of the procedure. Lashanda Spencer, individually and as ad-ministratrix of Stewart’s estate, filed this action against Goodill. She claimed that Goodill violated 18 Del. C. § 6852, the informed consent statute, by not telling Stewart that there was a risk of death. After a three day trial, the jury found that Spencer failed to prove causation, and the Superior Court entered judgment in favor of Goodill. This appeal followed.

Discussion

The informed consent statute was enacted in 1976, as part of a “major modifi *554 cation[ ] to [the] legal system as it relates to health care malpractice claims. 1 It provides:

(a) No recovery of damages based upon a lack of informed consent shall be allowed in any action for medical negligence unless:
(1) The injury alleged involved a nonemergency treatment, procedure or surgery; and
(2) The injured party proved by a preponderance of the evidence that the health care provider did not supply information regarding such treatment ... to the extent customarily given to patients ... by other licensed health care providers in the same or similar field of medicine....
(b) In any action for medical negligence, in addition to other defenses provided by law, it shall be a defense [to an informed consent claim] that:
(1) A person of ordinary intelligence ... could reasonably be expected to appreciate ... hazards inherent in such treatment;
(2) The injured party assured the health care provider he or she would undergo the treatment regardless of the risk involved;
(3) It was reasonable for the health care provider to limit the extent of his or her disclosures of the risks of the treatment ... because further disclosure could be expected to affect ... the injured party’s condition.... 2

The term “informed consent” means:

[T]he consent ... given after the health care provider has informed the patient ... of the nature of the proposed procedure ... and of the risks and alternatives to treatment ... which a reasonable patient would consider material to the decision whether or not to undergo the treatment.... 3

The parties agree that, to prevail on an informed consent claim, plaintiff must prove that: 1) the health care provider failed to provide information about risks and alternatives customarily given to patients; 2) a reasonable person would have considered the undisclosed information material; and 3) plaintiff was injured by a complication that should have been disclosed. The sole issue on appeal is whether plaintiff also must prove that a reasonable person would have declined the procedure if that person had been properly informed of the risks and alternatives. Because this is a question of law, our standard of review is de novo. 4

It is settled in Delaware that the failure to obtain informed consent is a form of medical malpractice. 5 Like other malpractice claims, an informed consent claim is one for negligence. 6 In general, to prove negligence one must establish that defendant breached a duty owed to plaintiff and that defendant’s act or omission proximately caused plaintiffs injury. 7 Proximate cause is defined as, “that direct cause without which the [injury] would not have occurred.” 8 Thus, unless the in *555 formed consent statute modifies the common law, plaintiff would have to prove that defendant’s failure to obtain informed consent was a proximate cause of plaintiffs injury. Stated another way, plaintiff would have to prove that a reasonable person would not have undergone the medical treatment if properly informed of the risks and alternatives.

Spencer argues that the informed consent statute has eliminated the need to establish proximate cause. She bases her argument on the plain language of the statute, which does not include any such requirement. In addition, Spencer relies on this Court’s decisions in Barriocanal v. Gibbs, 9 and Himes v. Gabriel, 10 and Superior Court Civil Pattern Jury Instruction § 7.2, as support for her position. Spencer’s contentions do not bear scrutiny.

One of the basic rules of statutory construction is that, “if [a] statute is unambiguous, there is no room for interpretation, and the plain meaning of the words controls.” 11 As Spencer notes, the informed consent statute only requires a plaintiff to establish that: 1) the doctor breached the standard of care by failing to provide information customarily given to patients about the procedure, the risks, and the alternatives; and 2) a reasonable patient would consider that information material to his or her decision. Since the statute is unambiguous, she argues that a causation requirement should not be read into it.

There are two problems with this argument.

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Bluebook (online)
17 A.3d 552, 2011 Del. LEXIS 179, 2011 WL 1312273, Counsel Stack Legal Research, https://law.counselstack.com/opinion/spencer-v-goodill-del-2011.