Luettke v. St. Vincent Mercy Med. Ctr., Unpublished Decision (7-28-2006)

2006 Ohio 3872
CourtOhio Court of Appeals
DecidedJuly 28, 2006
DocketCourt of Appeals No. L-05-1190, Trial Court No. CI-0200304833.
StatusUnpublished

This text of 2006 Ohio 3872 (Luettke v. St. Vincent Mercy Med. Ctr., Unpublished Decision (7-28-2006)) is published on Counsel Stack Legal Research, covering Ohio Court of Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Luettke v. St. Vincent Mercy Med. Ctr., Unpublished Decision (7-28-2006), 2006 Ohio 3872 (Ohio Ct. App. 2006).

Opinion

DECISION AND JUDGMENT ENTRY
{¶ 1} This case is before the court on appeal from the judgment of the Lucas County Court of Common Pleas, wherein a jury found in favor of appellees John Dooner, M.D., Joan Eischen, CRNA ("CRNA Eischen"), and Associated Anesthesiologists of Toledo, Inc. ("AAT"). Appellant, Joanne M. Luettke, appeals the April 29, 2005 jury verdict and asserts the following assignments of error:

{¶ 2} I. "The trial court erred and abused its discretion in granting the defendants' motion in limine, and excluding any evidence of St. Vincent's `Resident Manual' and `Rules and Regulations of the Medical Staff.'"

{¶ 3} II. "The verdict of the jury is against the manifest weight of the evidence."

{¶ 4} III. "The trial court erred in its instructions to the jury, and in its refusal to submit appellant's requested jury instructions."

{¶ 5} In early 2001, appellant was diagnosed with a paraesophageal hernia. This type of hernia occurs when a portion of the stomach comes up into the chest, behind the heart. Joseph Sferra, M.D., a general surgeon, recommended that appellant undergo a Nissen fundoplication surgery to correct the hernia.

{¶ 6} During the surgery, an esophageal dilator device known as a "bougie" is routinely passed down the esophagus and used as a sizer to make sure that when the wrap is performed the opening of the esophagus remains wide enough so that the patient can swallow freely. The bougies come in a series of diameters to accommodate each individual patient's esophagus. In Toledo, the general practice is that the anesthesia team passes the bougie at the surgeon's request.

{¶ 7} Appellant was admitted to St. Vincent Mercy Medical Center ("St. Vincent") on March 1, 2001 for her surgery. In the pre-operative waiting area, appellant met Sherrie Lynn who introduced herself as follows:

{¶ 8} "Good morning. My name is Sherrie. I am a registered nurse with the anesthesia department, and I will be one of the people taking care of you today. I am working with Joan Eischen who is a nurse anesthetist, and Dr. Dooner is the anesthesiologist who is working with us as well."

{¶ 9} Lynn was a registered nurse, enrolled as a student in the certified registered nurse anesthetist ("CRNA") training program at Wayne State University. Through an affiliation program with St. Vincent, students in the Wayne State program participate in clinical training at the hospital. Dr. Dooner, CRNA Eischen and Lynn understood that Lynn would be performing all of the anesthesia related procedures in appellant's surgery from beginning to end. However, Lynn did not identify herself to appellant as a student in training, nor did she discuss with appellant that she would be performing all anesthesia aspects of the surgery.

{¶ 10} When surgery commenced, Dr. Dooner instructed Lynn to perform the induction and intubation of appellant. After this was accomplished, Dr. Dooner left the operating room. He did not return until he was called back, more than an hour and a half later, after complications arose.

{¶ 11} Once appellant was anesthetized, Dr. Sferra requested that the anesthesia team pass the bougie down appellant's esophagus. Under the supervision of CRNA Eischen, Lynn successfully passed a size 40 bougie. Dr. Sferra determined the device was within the esophagus and told Lynn to remove it and insert a larger, size 44 bougie to further dilate appellant's esophagus. Lynn inserted the device and indicated that it had been placed at a sufficient distance that it should have been perceptible in the operative field. Dr. Sferra, however, could not see the bougie. Lynn then withdrew the bougie and attempted to pass it a second time. Again, Dr. Sferra was unable to see it. CRNA Eischen then attempted to insert the device, but it was still not perceptible in the operative field. Dr. Sferra then suggested that Dr. Dooner be called back into the operating room.

{¶ 12} Dr. Dooner arrived back in the room and was briefed on the situation. Suspecting a perforation of appellant's esophagus at this point in time, Dr. Sferra requested that Dr. Dooner pass the bougie. Dr. Dooner attempted the procedure, but again Dr. Sferra was not able to perceive the device in appellant's esophagus. Dr. Sferra began to manipulate the esophagus and saw that the bougie was outside the esophagus. Upon confirming that the device had in fact perforated appellant's esophagus, Dr. Sferra immediately consulted with a cardiothoracic surgeon at St. Vincent. They concluded appellant's surgery would have to be converted to an "open" procedure, which involved an incision in the abdomen as opposed to using a laparoscope. Surgery was performed to repair the esophagus at that time as well.

{¶ 13} Due to the perforation and the repair, it was necessary to put appellant on a feeding tube and keep her in a "coma-like state" for four days. Fluids accumulated in appellant's lungs and were evacuated. She also developed blood clots in her arms. It took three to four days before appellant was stable enough to be removed from the ventilator. Following the perforation, appellant experienced severe pain, gagging, nausea, loss of appetite, poor esophageal motility, and depression. Two months after the procedure, appellant was still unable to eat on her own and was continuously nourished through feeding tubes.

{¶ 14} As a result of appellant's complications, she was admitted to the University of Michigan Hospital where it was determined that she had no esophageal motility, as well as anxiety and depression. Appellant's depression was so severe that she required electric shock therapy, which caused severe memory loss and was subsequently discontinued as a result. Appellant continues to choke and gag when she eats and is afraid to go out to eat in public because of the symptoms.

{¶ 15} Subsequently, appellant filed suit against appellees CRNA Eischen, Dr. Dooner and his professional practice group, AAT. Also named as defendants were student nurse Lynn and St. Vincent.1 Appellant asserted claims for medical malpractice and informed consent.

{¶ 16} Prior to trial, the trial court granted, in part, appellees' motion in limine, which excluded any evidence and/or testimony with respect to the policies, provisions, and standards concerning the supervision of anesthesia procedures performed by students, informed consent for student participation, and patient rights, as set forth within St. Vincent's Resident Manual ("Manual") and Rules and Regulations of the Medical Staff ("Regulations"). Appellant's claims were ultimately tried to a jury which returned a verdict in favor of appellees on all counts. This appeal now follows.

{¶ 17} In her Assignment of Error No. I, appellant argues that the trial court abused its discretion in granting appellees' motion in limine and excluding any evidence of St. Vincent's Manual and Regulations.

{¶ 18} Appellant repeatedly attempted to introduce as evidence both the Manual and Regulations to demonstrate that St. Vincent established a specific standard of care to be followed by the entire medical staff and that appellees violated that standard. The Manual contains safety standards of care promulgated by St. Vincent for the supervision and responsibilities of students in training. The Manual provides, in part, that:

{¶ 19}

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Bluebook (online)
2006 Ohio 3872, Counsel Stack Legal Research, https://law.counselstack.com/opinion/luettke-v-st-vincent-mercy-med-ctr-unpublished-decision-7-28-2006-ohioctapp-2006.