Hawkins v. Rosenbloom

17 S.W.3d 116, 2000 WL 623195
CourtCourt of Appeals of Kentucky
DecidedMay 10, 2000
Docket1997-CA-002972-MR
StatusPublished
Cited by10 cases

This text of 17 S.W.3d 116 (Hawkins v. Rosenbloom) is published on Counsel Stack Legal Research, covering Court of Appeals of Kentucky primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Hawkins v. Rosenbloom, 17 S.W.3d 116, 2000 WL 623195 (Ky. Ct. App. 2000).

Opinion

OPINION

GUIDUGLI, Judge.

This is an appeal by Robert A. Hawkins and Yvonne Hawkins (Hawkinses) from a judgment order, pursuant to a jury verdict *118 of the Jefferson Circuit Court, which entered judgment for the appellee, Philip Rosenbloom, M.D. (Dr. Rosenbloom), and assessed ah costs against the Hawkinses. We affirm in part, reverse in part, and remand.

On January 28, 1994, Dr. Rosenbloom performed elective gallbladder surgery on Mr. Hawkins at Baptist East Hospital in Louisville, Kentucky. On January 11, 1994, prior to undergoing gallbladder surgery, Mr. Hawkins met with Dr. Rosen-bloom to discuss the general risks of surgery. As a result of this meeting, Dr. Rosenbloom caused to be prepared an office note stating that the general risks of surgery were discussed with Mr. Hawkins. Furthermore, Mr. Hawkins signed an informed consent form that stated his physician discussed with him the general risks of surgery. To remove Mr. Hawkins’ gallbladder, Dr. Rosenbloom used a procedure called laparoscopic cholecystectomy, whereby several small incisions are made in the surgical area, a laparoscope is inserted into one and the gallbladder is removed through the others. Laparascopic cholecystectomy is generally the preferred method of cholecystectomy (removal of gallbladder) as opposed to open cholecys-tectomy, whereby one’s gallbladder is removed through a single standard incision.

Mr. Hawkins was scheduled for release from the hospital on January 30, 1994. However, Mrs. Hawkins discovered drainage around the laparoscopic incisions and the discharge was canceled. Thereafter, Dr. Rosenbloom performed exploratory surgery on Mr. Hawkins and discovered that a 1.5-cm perforation had been cut into Mr. Hawkins’ bowel and that the bowel was leaking fecal material into Mr. Hawkins’ abdomen. On February 4, 1994, Dr. Rosenbloom drained two abscesses due to infection caused by the leaking bowel. Mr. Hawkins remained in the hospital seventeen (17) days and thereafter was released with a full colostomy. On May 12, 1995, Mr. Hawkins underwent a fourth surgery to close the colostomy, which proved unsuccessful. However, the colostomy closed on its own several months later. In April of 1997, Mr. Hawkins underwent a fifth surgery for repair of a double hernia that was related directly to his January 30,1994, colostomy.

The Hawkinses sued Dr. Rosenbloom for lack of informed consent and negligence among other things. The case went to trial and resulted in a jury verdict in favor of Dr. Rosenbloom. The Hawkinses raise three issues on appeal. First, before the trial of this matter, the trial court granted Dr. Rosenbloom’s motion in limine excluding any evidence regarding informed consent at trial. The trial court granted said motion because the Hawkinses did not have an expert witness to testify with regard to the standard of care that an ordinary and careful physician would follow in obtaining informed consent. Furthermore, the trial court refused to instruct the jury on the law of informed consent. Second, the trial court refused to allow the Hawkinses’ attorney to play video excerpts of testimony at trial during closing arguments. Third, during the trial of this matter, the trial court allowed Dr. Rosen-bloom’s attorney to cross-examine the Hawkinses’ expert witness, Dr. Marco Bonta (Dr. Bonta), with a notarized letter from another physician.

With regard to their first argument, the Hawkinses maintain that no expert testimony was needed to establish the standard of care for informed consent. The law of informed consent, KRS 304.40-320, states as follows:

In any action brought for treating, examining, or operating on a claimant wherein the claimant’s informed consent is an element, the claimant’s informed consent shall be deemed to have been given where:
(1) The action of the health care provider in obtaining the consent of the patient or another person authorized to give consent for the patient was in accordance with the accepted standard of medical or dental practice among mem *119 bers of the profession with similar training and experience; and
(2) A reasonable individual, from the information provided by the health care provider under the circumstances, would have a general understanding of the procedure and medically or dentally acceptable alternative procedures or treatments and substantial risks and hazards inherent on the proposed treatment or procedures which are recognized among other health care providers who perform similar treatments or procedures;
(8) In an emergency situation where consent of the patient cannot reasonably be obtained before providing health care services, there is no requirement that a health care provider obtain a previous consent.

Part (2) deals specifically with what a reasonable person should be told before deemed to have been given informed consent. The Hawkinses’ argument on this issue is two-fold. First, they argue that KRS 304.40-820 requires that a physician must meet the standard set out in both parts (1) and (2) of the statute for valid informed consent. Second, they argue that “the question of what a reasonable individual would understand does not require expert testimony.” Therefore, they maintain, the trial court should have allowed them to present the issue of informed consent to the jury without expert testimony because Dr. Rosenbloom did not meet the standard set out under part (2) of the statute.

An action based on lack of informed consent “is in reality one for negligence in failing to conform to a proper professional standard.... ” Holton v. Pfingst, Ky., 534 S.W.2d 786, 788 (1975). As in any medical malpractice case, the general rule is that expert testimony is required to negate informed consent. Keel v. St. Elizabeth Medical Center, Ky., 842 S.W.2d 860, 862 (1992). In Keel, the hospital administered a CT scan that involved injecting a contrast dye into the patient’s system. The patient later developed thrombophlebitis at the site of the injection. The Supreme Court found that expert testimony was not required to establish informed consent in this case because the patient was given absolutely no information whatsoever regarding the risks and hazards of the procedure. Id. In holding that expert testimony was not needed to establish informed consent in this case, the Court stated:

If we are to analogize consent actions to negligence actions, we must also acknowledge that a failure adequately to inform the patient need not be established by expert testimony where the failure is so apparent that layman may easily recognize it or infer it from evidence within the realm of common knowledge.

Id. (citations omitted). Thus, Keel is limited in its application to situations where no information is given to the patient regarding the risks and hazards of the procedure.

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Cite This Page — Counsel Stack

Bluebook (online)
17 S.W.3d 116, 2000 WL 623195, Counsel Stack Legal Research, https://law.counselstack.com/opinion/hawkins-v-rosenbloom-kyctapp-2000.