Call v. Keiter

2010 UT App 55, 230 P.3d 128, 651 Utah Adv. Rep. 17, 2010 Utah App. LEXIS 61, 2010 WL 816171
CourtCourt of Appeals of Utah
DecidedMarch 11, 2010
Docket20090051-CA
StatusPublished
Cited by1 cases

This text of 2010 UT App 55 (Call v. Keiter) is published on Counsel Stack Legal Research, covering Court of Appeals of Utah primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Call v. Keiter, 2010 UT App 55, 230 P.3d 128, 651 Utah Adv. Rep. 17, 2010 Utah App. LEXIS 61, 2010 WL 816171 (Utah Ct. App. 2010).

Opinion

OPINION

BENCH, Senior Judge:

¶ 1 Defendant John E. Keiter (Doctor) appeals the trial court’s denial of his motions for summary judgment, apportionment of fault, and directed verdict in a medical malpractice suit brought against him by Plaintiff Sharlene Call (Patient). We decline to address the directed verdict issue because Doctor has not marshaled the evidence. See generally Brewer v. Denver & Rio Grande W. R.R., 2001 UT 77, ¶33, 31 P.3d 557. We affirm the trial court’s denial of Doctor’s motions for summary judgment and apportionment of fault.

BACKGROUND

¶ 2 Patient was born with a chest deformity called pectus excavatum, also known as sunken chest syndrome. Her first reconstructive surgery for this condition was performed when she was three years old. In 1981, when Patient was in her early twenties, Doctor first treated Patient by modifying the original reconstructive surgery. Doctor also performed breast augmentation surgery, inserting silicone implants so that Patient’s chest would protrude more normally.

¶ 3 In 1995, after fourteen years without incident, Patient felt a pop in her left breast while being hugged. Later, upon feeling some lumpiness in her left breast, Patient returned to Doctor, who confirmed that the left implant had ruptured and was leaking silicone. Doctor performed surgery, removing a silicone granuloma — a mass of inflamed tissue that forms around silicone. Doctor also replaced both silicone implants with saline implants. In removing the left silicone *130 implant, Doctor did not remove its surrounding scar tissue capsule, which had collapsed and remained in Patient’s left breast. Following this surgery, Doctor informed Patient that he was unable to remove all of the residual silicone and warned her that more silicone granulomas could form in the future. In 1999, Patient found another lump in her left breast. Doctor performed surgery, removing another silicone granuloma. During this surgery, Doctor also removed Patient’s left saline implant, cleaned it, and reinserted it.

¶ 4 In 2000, Patient sought treatment from Doctor for a small, discolored hole that had developed below her left breast. On December 18, 2000, Doctor performed another surgery wherein he removed, cleaned, and reinserted the left saline implant and attempted to close the small, discolored hole. A culture obtained from this surgery indicated the presence of staphylococcus epidermidis — a staphylococcus bacteria that is commonly present on the skin and typically harmless but can become more virulent when present inside the body. Shortly after this surgery, the hole reopened to about the size of a quarter or fifty-cent piece, exposing the saline implant to view. On December 28, 2000, during an in-office procedure, Doctor determined that the implant had to be removed and decided to drain and remove the implant through the hole. As Doctor attempted to drain the implant by puncturing it with a needle, he hit and drained a large pocket of infection. Once the implant had been drained and removed, Doctor did not take any additional measures to determine the cause of the hole, such as requesting another culture or performing a more invasive procedure to explore the interior of Patient’s left breast. Doctor did not prescribe any additional antibiotics or other medications following this procedure, instead telling Patient to complete the remainder of her antibiotic prescription from the previous surgery, of which prescription there were only three days left.

¶ 5 The wound took several months to heal. During this time, Patient suffered from fever, night sweats, and pain and complained of bad-smelling drainage seeping out of the hole. Patient also had a difficult time contacting Doctor. When she finally managed to see Doctor in February 2001, the hole had still not healed, remaining two to three inches deep and the size of a fifty-cent piece. Doctor told Patient to clean the wound using peroxide and a Q-tip. When this treatment did not prove effective, Patient continually attempted to contact Doctor. She was told by Doctor’s staff to be patient and continue the peroxide and Q-tip treatment. By May 2001, the wound closed and appeared to have healed, and Doctor determined that he could attempt to insert another implant.

¶ 6 In August 2001, Doctor performed surgery to insert a new saline implant into Patient’s left breast. During this surgery, Doctor noted that a white substance consistent with silicone was present in Patient’s breast tissue; however, Doctor merely observed this silicone and made no attempt to remove it. Within a couple months, Patient discovered that another hole had formed in the same location. In October 2001, Doctor removed the latest implant through the hole. Shortly thereafter, Patient sought treatment from other doctors.

¶ 7 In October 2002, Patient commenced this action by serving Doctor with a notice of intent to commence action. . Patient then filed her complaint against Doctor for medical malpractice in April 2003.

¶ 8 In support of her claims, Patient presented expert testimony from Dr. Robert T. Miner (Expert). In forming his opinions, Expert evaluated Doctor’s course of treatment of Patient since 1995. Expert considered the rupture of Patient’s silicone implant and explained that the scar tissue capsule and residual silicone are both a potential nidus or nest for bacteria. If not properly removed, Expert explained, these materials could become a host for a latent, recurring infection. Expert opined that by removing the scar tissue capsule — a procedure called a capsulectomy — much of the residual silicone remaining encapsulized could also be removed. However, Expert allowed that it would be impossible to remove all of the residual silicone, especially if the scar tissue capsule had not remained intact and the silicone had leaked into the surrounding breast tissue.

*131 ¶ 9 Expert also considered the hole that developed on the bottom of Patient’s left breast in December 2000 and explained that such a hole surrounded by discolored tissue is a “classic” sign of implant extrusion, wherein the body pushes out a foreign object, typically in response to an infection. Expert further considered the second extrusion in October 2001 — following Doctor’s determination in May 2001 that Patient’s wound had healed — and explained that if an infected area is not properly cleaned, the skin may heal over an infection, sealing it inside.

¶ 10 Based on these evaluations, Expert opined that Doctor’s treatment of Patient’s infection fell below the applicable standard of care. First, Expert testified that in December 2000, Doctor should have identified the hole as an implant extrusion due to infection. In forming this opinion, Expert was critical of Doctor’s lack of concern about and investigation into Patient’s symptoms. Second, Expert testified that Doctor should have known that the scar tissue capsule was present in Patient’s left breast and recognized its potential as a host for a latent, recurring infection. Third, Expert testified that before ever inserting another implant, Doctor should have cleaned out the infected area by performing a capsulectomy then draining the wound to prevent the skin from healing over the infected area.

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Cite This Page — Counsel Stack

Bluebook (online)
2010 UT App 55, 230 P.3d 128, 651 Utah Adv. Rep. 17, 2010 Utah App. LEXIS 61, 2010 WL 816171, Counsel Stack Legal Research, https://law.counselstack.com/opinion/call-v-keiter-utahctapp-2010.