Jaki Holzer v. Ascension Providence Rochester

CourtMichigan Court of Appeals
DecidedJuly 10, 2025
Docket369402
StatusUnpublished

This text of Jaki Holzer v. Ascension Providence Rochester (Jaki Holzer v. Ascension Providence Rochester) is published on Counsel Stack Legal Research, covering Michigan Court of Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Jaki Holzer v. Ascension Providence Rochester, (Mich. Ct. App. 2025).

Opinion

If this opinion indicates that it is “FOR PUBLICATION,” it is subject to revision until final publication in the Michigan Appeals Reports.

STATE OF MICHIGAN

COURT OF APPEALS

JAKI HOLZER and ROBERT HOLZER, UNPUBLISHED July 10, 2025 Plaintiffs-Appellants, 11:30 AM

v No. 369402 Oakland Circuit Court ASCENSION PROVIDENCE ROCHESTER d/b/a LC No. 2019-176257-NH CRITTENDON HOSPITAL MEDICAL CENTER and ASCENSION CRITTENDON HOSPITAL, and JEFFREY SHULAK, M.D.,

Defendants-Appellees.

Before: MALDONADO, P.J., and BOONSTRA and WALLACE, JJ.

PER CURIAM.

Plaintiffs bring this appeal of right from the trial court’s December 27, 2023 order granting summary disposition pursuant to MCR 2.116(C)(10) of Jaki Holzer’s medical malpractice claim and Robert Holzer’s derivative loss of consortium claim.1 The trial court found that “although there may be a question of fact regarding the breach of standard of care,” the plaintiff in a medical malpractice case must establish the alleged breach was a proximate cause of the alleged injury. It further found that “here there is no causal nexus between the puncture [of the subject saline breast implant and] the plaintiff’s alleged pain and therefore plaintiff has failed to produce expert testimony to support that injury.” In other words, the trial court found plaintiff failed to establish a genuine issue of material fact as to the element of “proximate causation between the alleged breach and the injury.” Elher v Misra, 499 Mich 1, 21; 878 NW2d 790 (2016). Because we find that there is a genuine issue of material fact for the jury’s resolution on the issue of whether defendant Jeffrey Shulak, M.D.’s alleged breach of the standard of care proximately caused

1 Because the issues on appeal here pertain only to her medical malpractice claim, hereinafter “plaintiff” shall refer to Jaki Holzer.

-1- plaintiff’s injuries,2 including pain resulting from the two implant removal and replacement surgeries, we reverse and remand for further proceedings.

I. FACTUAL AND PROCEDURAL HISTORY

Plaintiff underwent an elective procedure to have bilateral breast augmentation by way of saline breast implants in 2005. In January 2017, plaintiff complained of right breast pain to her OB/GYN and he ordered a diagnostic mammogram and right breast ultrasound. The February 2017 mammogram showed cysts and a nodule that were “[p]robably benign.” Plaintiff was presented with the option to have another mammogram in six months or to have an immediate aspiration / biopsy confirmation, and she chose the latter.

On March 27, 2017, Dr. Jeffrey Shulak performed an ultrasound image guided biopsy of what he believed to be the breast lesions and nodule recommended for intervention. While Dr. Shulak did not have any trouble seeing the lesions and nodule with ultrasound, when he attempted to obtain a biopsy employing a vacuum-assisted Mammotome device,3 he had difficulty getting the needle properly placed. Plaintiff’s expert diagnostic radiologist, Dr. Ronald Washburn, reviewed the ultrasound images from the procedure and said that they show that the Mammotome “needle is all over the place.” He also said that, in some of the ultrasound images, the Mammotome needle is nowhere near the nodule that was to be biopsied. Dr. Washburn acknowledged that none of the ultrasound images from the procedure that Dr. Shulak chose to capture depict the biopsy needle within or inside the breast implant.

Another mammogram was performed upon plaintiff immediately following the biopsy procedure. According to Dr. Washburn, it showed evidence of a puncture, rupture or leakage from the right implant that was not present in her earlier February 17, 2017 mammogram. He said “you see what appears to be some collapse of the implant, because there’s more linear folds,” “infolding or an invagination,” and a “lumpy bumpy appearance.” Dr. Washburn testified that lucent marks on the imaging from the mammogram that occurred immediately following the surgery more likely than not depicted “dots of air inside the implant” caused by the bore of the outer Mammotome needle when it punctured the surface of the implant.

Dr. Washburn noted plaintiff’s testimony that “after the biopsy she had a lot of pain and she was bleeding.” In light of this, and the appearance of the right implant in the mammogram immediately following the biopsy procedure, Dr. Washburn testified defendant Dr. Shulak’s

2 Plaintiffs’ claims against defendant Ascension Providence Rochester Hospital are based upon its vicarious liability for Dr. Shulak’s alleged medical negligence. 3 Dr. Washburn testified that the Mammotome device employed in this procedure is a needle within a needle, or a sleeve within a sleeve . . . , and there is a side opening that’s maybe a millimeter in length. And what happens is, is the inside sleeve, it’s retracted slightly. And when the needle is advanced and it’s inside the tissue, you then apply the vacuum to the needle; and in that side port . . . , the vacuum sucks tissue into the bore of the needle. The inside sleeve cuts it off, and you have the tissue inside the needle, and then you take the needle out and there is your [biopsy].

-2- “breach of the standard care would be a puncture with leakage of saline into the tissue. Saline is saltwater. If you put salt in a wound, it’s going to hurt.” According to Dr. Washburn, this breach “necessarily led to a noticeable and visible deformity of the right breast that could only be remedied with further surgery.”

Plaintiff testified that she tasted salty water coming up into her mouth on the day following the biopsy procedure, March 28, 2017. She likewise observed that her right breast looked deflated and incongruous with her other breast at that time. She sought advice and treatment from her plastic surgeon, Dr. Chau, who advised removal and replacement of both of the implants. She told Dr. Chau about the pain she had been experiencing since the biopsy procedure and he indicated it was probably due to the deflated implant being folded or positioned in a manner where it rubs on her bra.

Dr. Chau testified that, when plaintiff presented to him on April 24, 2017, her breasts very obviously appeared lopsided and asymmetrical, “because the right side had deflation of the implant,” and he recommended removal and replacement of both the implants. Dr. Chau recommended bilateral removal and replacement due to the age of the original implants. He performed this procedure on August 11, 2017 and testified that the right breast implant “was ruptured and I replaced it.” Dr. Chau then had to perform yet another removal and replacement of the right breast implant on August 21, 2017, because the initial replacement was leaking. Dr. Chau acknowledged that there is “severe pain” right after the removal and replacement procedures plaintiff underwent, but that the pain usually subsides once the patient recovers.

Plaintiff testified that, following the two removal and replacement procedures, she experienced and has continued to experience constant pain on the right side of her chest (extending through the core of her body to her back) and a limited range of motion, due to which she can no longer take part in activities she previously engaged such as stretching, yoga, landscaping and home improvement projects. She testified that her ongoing pain and limited range of motion is exhausting, embarrassing, causes her anxiety and difficulty sleeping.

Before the initial August 11, 2017 removal and replacement procedure was performed, plaintiff, by way of a letter from her attorney investigating Dr. Shulak’s potential medical malpractice, requested that Dr. Chau remove the implants without causing any further damage to them, and that they be preserved and provided to plaintiff following their removal. Dr.

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