Susan Lucas v. Ochsner Clinic Foundation, Ochsner Medical Center-Westbank, L.L.C.
This text of Susan Lucas v. Ochsner Clinic Foundation, Ochsner Medical Center-Westbank, L.L.C. (Susan Lucas v. Ochsner Clinic Foundation, Ochsner Medical Center-Westbank, L.L.C.) is published on Counsel Stack Legal Research, covering Louisiana Court of Appeal primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Opinion
SUSAN LUCAS, ET AL. * NO. 2024-C-0628
VERSUS * COURT OF APPEAL OCHSNER CLINIC * FOUNDATION, OCHSNER FOURTH CIRCUIT MEDICAL CENTER- * WESTBANK, L.L.C., ET AL. STATE OF LOUISIANA *******
APPLICATION FOR WRITS DIRECTED TO CIVIL DISTRICT COURT, ORLEANS PARISH NO. 17-415, DIVISION “L” Honorable Kern A. Reese, Judge ****** Judge Roland L. Belsome ****** (Court composed of Judge Roland L. Belsome, Judge Daniel L. Dysart, Judge Dale N. Atkins)
Atkins, J., concurs in the result.
Kara Hadican Samuels Jennifer L. Thornton 4004 Canal Street New Orleans, LA 70119
COUNSEL FOR PLAINTIFF / RELATORS,
Don S. McKinney William K. Wright IV 701 Poydras Street, Suite 4500 New Orleans, LA 70139
COUNSEL FOR RESPONDENTS, OCHSNER CLINIC FOUNDATION AND JOHN SPERA, C.R.N.A.
WRIT GRANTED, RELIEF GRANTED October 10, 2024 RLB The relator in this writ application seeks review of the trial court’s denial of
DLD a motion in limine that would have excluded any mention of informed consent in
this medical malpractice case.
Fact summary
Dorothy Caserta (“Caserta”), the decedent in this wrongful death and
survival action case was suffering from aortoiliac occlusive disease1. She elected
to have aortic reconstruction surgery as a treatment for this condition. The surgery
was to be performed at Ochsner Westbank Medical Center on July 17, 2013. In
anticipation of the surgery, Caserta signed consent forms that acknowledged
certain risks of the proposed surgery and authorized the medical providers to
proceed with that knowledge. The consent forms are part of Caserta’s medical
records. Neither the consent to the surgery nor the acknowledgment of the risks is
contested by Plaintiffs’ claim.
The surgery proceeded on the date planned. Caserta was given general
anesthesia by the routine insertion of a nasogastric tube (“NG tube”). During the
course of the surgery, the surgeon discovered that the NG tube had made a 6
1 Aortoiliac occlusive disease is a type of peripheral artery disease that occurs when the aorta or
iliac arteries become blocked or narrowed. This blockage can be caused by a buildup of plaque in the walls of the blood vessels.
1 centimeter tear in Caserta’s esophagus. The surgeon immediately repaired the
trachea.2 However, due to blood loss and other complications, Caserta died in the
hospital on August 15, 2013.
Trial court proceedings
Plaintiffs are Caserta’s surviving adult children and one grandchild. The
only defendants remaining in the suit are the hospital where the surgery was
initiated and the Certified Registered Nurse Anesthetist who inserted the NG tube.
Plaintiffs filed their motion in limine seeking to exclude all evidence relating
to informed consent. Essentially, Plaintiffs argue that they have not put informed
consent at issue in this litigation. Therefore, they contend, any testimony or
documents directed to that issue is of no relevance. Further, Plaintiffs add, even if
informed consent has any relevance to this action, the balance required by La. C.E.
art. 403 demands its exclusion because of the high probability of prejudice.
Defendants contend that the informed consent documents are part of
Caserta’s certified medical records and are therefore admissible. For their part,
Defendants do not believe that the evidence in question raises any great risk of
undue prejudice.
The trial court accepted the defendants’ arguments in orally issued reasons
and denied the motion in limine. Because of the limited amount of time until the
trial date, Plaintiffs have requested and received expedited review of their writ
application.
2 The injury to the trachea caused the surgeon to cancel the aortic reconstruction for which
Caserta was hospitalized.
2 Legal analysis
The issue raised in this application is part of a relatively new body of law in
our state. So far, there is no broad ruling from the Louisiana Supreme Court that
directs us to exclude evidence of informed consent in a medical malpractice case
when informed consent is not part of the claim presented.
A review of the application must begin with the basic rules of relevance and
admissibility. Relevant evidence is any evidence tending to make the existence of
a fact consequential to the determination of the action more or less probable than it
would be without the evidence. La. C.E. art. 401. As a general rule, all relevant
evidence is admissible. La. C.E. art. 402. This general rule, however, is tempered
by La. C.E. art. 403, which holds that, “Although relevant, evidence may be
excluded if its probative value is substantially outweighed by the danger of unfair
prejudice, confusion of the issues, or misleading the jury, or by considerations of
undue delay, or waste of time.”
In Matranga v. Parish Anesthesia of Jefferson, L.L.C., 2014-448 (La.
App. 5 Cir. 5/14/15); 170 So. 3d 1077, the trial court permitted the introduction of
documents granting consent for treatment. In a fact situation remarkably similar to
the one now before us, the patient / decedent died as a result of a rupture of the
trachea during insertion of an NG tube. The court noted that, at trial, “The
defendants repeatedly highlighted the dangers inherent in Ms. Greathouse’s
planned surgery…and equated those risks to the risks of her intubation. This link
could easily lead to the conclusion that Ms. Greathouse acquiesced to her
injury and subsequent death.” Id. at 1092. The Matranga court ultimately
determined that introduction of the informed consent evidence most likely caused
3 confusion to the jury. As a result, the court reversed the jury decision and
remanded the case for a new trial.
In Patten v. Gayle, 46,453 (La. App. 2 Cir. 6/22/11); 69 So. 3d 1180, the
court also found jury confusion as a result of introduction of irrelevant consent
forms and testimony. The court wrote, “A risk of bowel injury was among the
risks listed on the consent forms signed by Mrs. Patten. … Being injured as a result
of negligence by one’s physician is not a reasonably foreseeable risk of receiving
medical treatment.” Id. at 1187. In testimony, the defendant surgeon testified that
he had, in fact, caused injury to his patient when he pierced a portion of her small
bowel. The court concluded that the jury’s finding that the surgeon’s negligence
caused no injury to Mrs. Patten was manifestly erroneous and conducted a de novo
review of the facts of the case. After its review of the record, the Patten court
concluded that a later, second perforation of the patient’s bowel was not caused by
the surgeon. The appellate court found for the defendant just as the jury did but for
reasons that may have been completely different. Based on the procedural path
taken by the case, one can never determine whether the jury would have reached
the same verdict if informed consent evidence had been excluded.
In Matranga and Patten, the common thread is jury confusion. In one case,
the court found the confusion necessitated a new trial; in the other, the court
undertook a review of the facts itself. In both cases, a jury decision without the
confusion and possible prejudice caused by informed consent evidence would have
been preferable to the ultimate outcomes.
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