Rosenthal v. Bornstein

2025 IL App (1st) 240277-U
Appellate Court of Illinois·Decided November 7, 2025·No. 1-24-0277·Unpublished

Opinion

2025 IL App (1st) 240277-U SIXTH DIVISION

November 7, 2025

No. 1-24-0277

NOTICE: This order was filed under Supreme Court Rule 23 and is not precedent except in the limited circumstances allowed under Rule 23(e)(1).

IN THE

APPELLATE COURT OF ILLINOIS FIRST DISTRICT

LOGAN ROSENTHAL, as Independent Administrator of ) Appeal from the Circuit Court the ESTATE OF PHILLIP ROSENTHAL, deceased, ) of Cook County.

)

Plaintiff-Appellant, )

)

)

v. ) No. 20 L 2363 )

SCOTT BORNSTEIN, M.D. and EYE CARE LTD., ) Honorable ) Karen L. O’Malley, Defendants-Appellees. ) Judge, presiding.

PRESIDING JUSTICE C.A. WALKER delivered the judgment of the court.

Justices Pucinski and Hyman concurred in the judgment.

ORDER

¶1 Held: We affirm the jury’s verdict for defendants pursuant to the general verdict rule because plaintiff’s claims on appeal fail to challenge each ground on which the jury could have found for the defendants.

¶2 This case arises from medical treatment Phillip Rosenthal received from the defendant Dr. Scott Bornstein (whose medical group, Eye Care Ltd. (hereinafter, collectively, Bornstein) was also named as a defendant) on July 9, 2019. Phillip unfortunately passed away during the pendency of this litigation, and his son, Logan Rosenthal, assumed the role of plaintiff as the independent administrator of Phillip’s estate. During the treatment at issue, Bornstein treated Phillip for shingles by prescribing Valacyclovir, commonly known as Valtrex. According to Phillip, Bornstein ordered the wrong dosage by failing to properly account for Phillip’s pre-existing conditions (including renal failure needing dialysis). Bornstein’s prescription was one gram of Valtrex every 8 hours. Phillip experienced symptoms including an altered mental state shortly after the visit and presented to Glenbrook Hospital on July 11, 2019. This resulted in an extended hospitalization in multiple facilities that lasted until August 9, 2019. Phillip was then discharged to Brentwood, a rehabilitation facility, where he remained until September 2019. Bornstein maintained that his dosage was appropriate, the record did not show Phillip suffered from Valtrex toxicity and, if he did, it was not the cause of the hospitalization. In making these defenses, Bornstein pointed to other medical conditions Phillip was suffering from in July 2019, including a bacterial infection in his liver that spread to his lungs, which was discovered during the hospitalization.

¶3 Following trial, the jury ruled generally in Bornstein’s favor as there were no special interrogatories. Logan now appeals, arguing that the circuit court erred by admitting evidence regarding two issues: (1) Bornstein’s testimony at trial that he complied with the standard of care by consulting the Physician’s Desk Reference (PDR) during his treatment (and the admission of corresponding expert testimony), and (2) references during trial, elicited by defense counsel, of three conditions mentioned in Phillip’s medical records as part of his differential diagnosis

(meningitis, meningoencephalitis, and encephalitis), which he maintains should have been barred because Bornstein never disclosed expert opinion that any of those three conditions caused Phillip’s hospitalization. We affirm the jury’s verdict because, as explained below, Logan’s claims on appeal do not challenge each defense theory raised by Bornstein that could independently support the jury’s verdict.

¶4 BACKGROUND

¶5 In his initial complaint, filed on February 26, 2020, Phillip brought a claim for professional negligence, alleging that on July 9, 2019, Bornstein “inappropriately prescribed Valtrex,” which proximately caused him injury. On August 20, 2020, Logan filed a motion to spread Phillip’s death of record. Logan than amended the complaint, assuming the role of plaintiff as the independent administrator of Phillip’s estate and adding wrongful death and survival counts. The circuit court later granted Bornstein’s motion for summary judgment on the wrongful death claim.

¶6 In Bornstein’s pretrial disclosures pursuant to Illinois Supreme Court Rule 213(f) (eff. Jan. 1, 2018), he listed himself as a Rule 213(f)(3) controlled expert witness, and disclosed, in relevant part, that he would “testify consistently with the medical records, his custom and practice, and his independent recollection,” and was “expected to testify regarding the care and treatment of plaintiff’s decedent.”

¶7 Bornstein disclosed additional witnesses, including, in relevant part, Dr. John Segreti as a Rule 213(f)(3) expert in infectious disease. Segreti was expected to testify that, “based on the decedent’s medical records, the dosage of Valtrex *** was neither a cause nor contributing cause of the decedent’s admission to Glenbrook North Hospital and elongated stay at Glenbrook North and Brentwood.*** Instead of Valtrex, Dr. Segreti will explain the cause of the extended hospital admission was the decedent’s liver abscess, which grew pseudomonas, and the development of

sepsis, and decortication. *** Dr. Segreti will explain the decedent’s altered mental status resulted from sepsis, not Valtrex.”

¶8 Additionally, Bornstein listed Dr. Frank Paloucek, a toxicologist, as a Rule 213(f)(3) expert who was expected to testify that “there was no clinical overdose or toxicity” from Valtrex and the drug “was neither a cause nor a contributing cause of the decedent’s admission to Glenbrook North Hospital and elongated stay at Glenbrook North and Brentwood.” Finally, Dr. Kathleen Scarpulla, an ophthalmologist, was expected to testify that Bornstein’s conduct complied with the standard of care, in part because he “acted reasonably by consulting the PDR.”

¶9 During the discovery process, Bornstein testified at his discovery deposition as follows:

“LOGAN’S COUNSEL: Did you review the PDR or the dosage recommendations from the manufacturer of Valtrex, did you review that?

BORNSTEIN: Can you be more specific?

Q: Sure. Have you reviewed the PDR in relationship to dosage recommendations for patients with end-stage renal disease on hemodialysis?

A: I have in the past reviewed that.

Q: When was the last time you reviewed it?

A: I must have reviewed that when this deposition was arranged.

Q: Okay. So whenever we started talking about getting your deposition, you took – A: That would be the most recent time that I reviewed it. I have reviewed it in the past as well.”

¶ 10 Bornstein later responded to the question, “Based upon your review of the PDR, did you follow [the] recommendations [of the PDR] when you administered Valtrex***? with “Yes,” then continued:

“Mr. Rosenthal *** was on hemodialysis. And so if you look in the PDR, the recommendations for dosing changes are based on different levels of renal failure. He *** was at that point actually on dialysis. So he was not in one of those categories that’s for renal failure. He was past the point of renal failure and now being dialyzed. And so when you read through the PDR, it gives—if I recall—an area for hemodialysis patients and it

has a specific section on that that is outside of the guidelines of dosing changes in different degrees of renal failure.”

¶ 11 During Dr. Scarpulla’s discovery deposition, she testified in relevant part that it was her understanding that Bornstein looked up the dosage of Valtrex in the PDR on July 9, 2019, when he treated Phillip. When asked what she based this understanding on, she first stated Bornstein’s deposition and the medical records but later acknowledged she did not review Bornstein’s deposition before providing her opinions to defense counsel for inclusion in the Rule 213 disclosures. Instead, portions of her opinions were based on discussions she had with defense counsel, who “relayed to [her] that Dr. Bornstein had the checked the PDR and saw the dosing.”

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