Dills v. New Mexico Heart Institute, P.A.

2016 NMCA 23, 2016 NMCA 023, 9 N.M. 360
CourtNew Mexico Court of Appeals
DecidedDecember 23, 2015
DocketS-1-SC-35709; Docket 33,725
StatusPublished

This text of 2016 NMCA 23 (Dills v. New Mexico Heart Institute, P.A.) is published on Counsel Stack Legal Research, covering New Mexico Court of Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Dills v. New Mexico Heart Institute, P.A., 2016 NMCA 23, 2016 NMCA 023, 9 N.M. 360 (N.M. Ct. App. 2015).

Opinion

OPINION

WECHSLER, Judge.

{1} The opinion filed in this case on November 23, 2015 is hereby withdrawn and the following substituted therefor. Plaintiffs motion for rehearing is denied.

{2} In this medical malpractice case, we consider the propriety of the district court’s jury instruction concerning the obligation of a doctor to inform a patient of treatment alternatives. We hold that, under the facts of this case, the district court did not err by instructing the jury that a “doctor has no duty to discuss alternatives to and risks of treatment which the doctor can reasonably expect to be known to the patient.” Accordingly, we affirm.

BACKGROUND

{3} Plaintiff Ruth E. Dills had a history of tachybrady syndrome for which she received a pacemaker, with implanted leads, in 1996. She received a new pacemaker, manufactured by Medtronics, in 2006. Plaintiff went to the emergency department of the Heart Hospital in Albuquerque, New Mexico onFebruary 10, 2009 with a fractured lead placement. The following day, she met with Dr. Kathleen Blake at the New Mexico Heart Institute who recommended that Plaintiff have her pacemaker leads extracted and the generator replaced. Dr. Blake explained to Plaintiff the risks and benefits of the lead extraction procedure. On February 20, 2009, Plaintiff met with Dr. Luis Constantin who was to perform the procedure that day with Dr. Blake’s assistance. For reasons unrelated to this case, the procedure was rescheduled and performed on March 4, 2009. Plaintiff was discharged on March 6, 2009. She returned to the Heart Hospital emergency department three days later and was diagnosed with tricuspid valve regurgitation, atrial fibrillation, and right-sided congestive heart failure. She was admitted to the hospital in May 2009 and various procedures were performed, including open heart surgery to repair the torn tricuspid valve and other repairs to correct heart defects caused by her underlying heart disease process.

{4} Plaintiff brought this action against Defendant, which operates the Heart Hospital, alleging the medical malpractice of Defendant’s doctors and agents, Dr. Blake and Dr. Constantin. Plaintiff originally named Dr. Blake and Dr. Constantin as defendants, but, for reasons not related to this appeal, the claims against Dr. Constantin were dismissed, and Dr. Blake was granted summary judgment with respect to the claims against her.

{5} The gravamen of Plaintiff’s action, as relevant to this appeal, was that she was not informed of alternative procedures to the lead extraction proceditre and that the lead extraction procedure was not indicated under the circumstances. In this regard, Plaintiff maintained, among other things, that when she went to the Heart Hospital emergency department on February 10, 2009, checking by the Medtronics representative only indicated that one of the two pacemaker leads was malfunctioning and leaking current, not that the leads needed to be changed, and that checking the pacemaker again on the following day also did not confirm the need for lead replacement. Plaintiff further maintained that Dr. Blake did not inform Plaintiff of alternative courses of action, including “reprogramming the pacemaker to unipolar mode and capping and abandoning the existing leads and implanting new ones” and that Dr. Constantin also “did not provide Plaintiff with information regarding alternatives to [pacemaker] lead extraction.” Plaintiff contended, among other things, that Dr. Constantin damaged a leaflet on her tricuspid valve during the lead extraction procedure and that she developed severe pain from the pacemaker pocket Dr. Constantin made to implant an antibiotic pouch.

{6} At trial, two issues were presented to the jury: whether Dr. Constantin failed to offer and inform Plaintiff of alternatives to pacemaker lead extraction and whether Dr. Constantin performed a medical procedure, the lead extraction, that was not reasonably necessary for Plaintiffs condition. The jury returned a verdict for Defendant. Plaintiff appealed from the district court’s judgment. On appeal, this Court decided Plaintiff’s appeal in part by memorandum opinion on the summary calendar and assigned to the general calendar the single issue of whether the district court correctly instructed the jury concerning the law of informed consent.

FACTUAL BASIS UNDERLYING THE JURY INSTRUCTION

{7} While Plaintiff contended that neither Dr. Blake nor Dr. Constantin informed her of treatment alternatives to lead replacement, Defendant offered the testimony of the doctors at trial in support of its position that Plaintiff had been informed of treatment alternatives. Because Plaintiff did not originally designate trial transcripts for review on appeal, Defendant provided with its answer brief a transcript of the testimony of Dr. Blake in which she discussed her receipt of Plaintiff s informed consent. See Rule 12-211 (E) NMRA (“Each appellant shall be responsible for the timely preparation and filing of the transcript of proceedings.”). Defendant also referred to portions of Dr. Constantin’s deposition that Plaintiff discussed in her brief in chief on appeal. By way of motion, Plaintiff was permitted to supplement the record on appeal at the time of her reply brief with transcripts of Plaintiff’s trial testimony and the trial testimony of Dr. Constantin that was presented as part of Plaintiffs case. Plaintiff did not, however, supplement the record with Dr. Constantin’s trial testimony when he was called as a witness during Defendant’s case. 1

{8} Dr. Blake testified that she did not have an independent recollection of her conversation about informed consent with Plaintiff that had occurred seven years earlier. She testified, however, that she had obtained informed consent for a medical procedure from patients approximately 8,000 to 10,000 times and that she followed the same typical format to do so. She testified that she would routinely “talk about what the problem is and what the alternatives are for treating that problem and what the risks are for those alternatives, [and] what the benefits are.” She would have given Plaintiff three treatment options: (1) not to have taken any action and leaving the pacemaker programmed as it was, (2) surgically replacing the pacemaker ventricular lead, and (3) surgically extracting both leads and replacing them with new ones.

{9} Dr. B lake ’ s summary in her notes reflects that she discussed with Plaintiff “the need for lead extraction” and advised “that both leads be removed because we may otherwise be back in a short time from now to deal with an old worn-out lead.” The notes further state, “all questions answered, good understanding confirmed, and she agrees to proceed next week with me and Dr. Constantin.” Dr. Blake also testified that when she concluded her discussion with Plaintiff, she believed that she had “a full and thorough informed consent discussion with her.” She did not expect that Dr. Constantin “would then redo or do again another full informed consent discussion” because Plaintiff was Dr. Blake’s patient, with whom she had established a long-term relationship, and Dr. Blake was making the recommendation. In his deposition, Dr.

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Cite This Page — Counsel Stack

Bluebook (online)
2016 NMCA 23, 2016 NMCA 023, 9 N.M. 360, Counsel Stack Legal Research, https://law.counselstack.com/opinion/dills-v-new-mexico-heart-institute-pa-nmctapp-2015.