Grafilo v. Soorani

CourtCalifornia Court of Appeal
DecidedOctober 29, 2019
DocketB286912
StatusPublished

This text of Grafilo v. Soorani (Grafilo v. Soorani) is published on Counsel Stack Legal Research, covering California Court of Appeal primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Grafilo v. Soorani, (Cal. Ct. App. 2019).

Opinion

Filed 10/2/19; Certified for publication 10/29/19 (order attached)

IN THE COURT OF APPEAL OF THE STATE OF CALIFORNIA

SECOND APPELLATE DISTRICT

DIVISION TWO

DEAN GRAFILO, as Director, etc., B286912

Plaintiff and Respondent, (Los Angeles County Super. Ct. No. v. BS171127)

EMIL SOORANI,

Defendant and Appellant;

KIMBERLY KIRCHMEYER, as Executive Director, etc.,

Real Party in Interest.

APPEAL from an order of the Superior Court of Los Angeles County. Daniel S. Murphy, Judge. Affirmed.

Fenton Law Group, Benjamin J. Fenton, Dennis E. Lee and Alexandra de Rivera, for Defendant and Appellant.

No appearance for Plaintiff and Respondent. Xavier Becerra, Attorney General, Gloria L. Castro, Assistant Attorney General, Judith T. Alvarado and Christina Sein Goot, Deputy Attorneys General, for Real Party in Interest.

______________________________

Dr. Emil Soorani appeals from an order compelling the production of his patients’ medical records to the Medical Board of California (the Board). We affirm. FACTUAL AND PROCEDURAL BACKGROUND I. The Board’s Investigation Dr. Soorani is a psychiatrist who has been licensed by the Board as a physician and surgeon since 1981. After receiving “information that Dr. Soorani may be overprescribing controlled substances[,]” the Board initiated an investigation. The Board obtained a Controlled Substance Utilization Review and Evaluation System (CURES)1 report detailing Dr. Soorani’s prescribing history between June 1, 2012,

1 CURES “is California’s prescription drug monitoring program. By statute, every prescription of a Schedule II, III, or IV controlled substance must be logged in CURES, along with the patient’s name, address, telephone number, gender, date of birth, drug name, quantity, number of refills, and information about the prescribing physician and pharmacy. [Citation.]” (Lewis v. Superior Court (2017) 3 Cal.5th 561, 565 (Lewis).) The Board is authorized to access the CURES database (id. at p. 567), which is maintained by the California Department of Justice (id. at p. 566).

2 and June 16, 2015. Dr. Jill Klessig, the Board’s medical consultant, reviewed the CURES report and identified six of Dr. Soorani’s patients—T.M., L.R., A.S., M.J., R.B., and A.D. (collectively, the six patients)—who were prescribed controlled substances in large quantities or with “erratic patterns.” In Dr. Klessig’s opinion, obtaining and reviewing the medical records of the six patients were necessary to determine whether Dr. Soorani was excessively prescribing controlled substances in violation of the Medical Practice Act (Bus. & Prof. Code, § 2000 et seq.). In April 2016, a Board investigator sent letters to the six patients requesting that they contact him to schedule an interview “concerning the care and treatment” they received from Dr. Soorani. A medical release form was enclosed that, if signed, would authorize Dr. Soorani to disclose all of their medical records to the Department of Consumer Affairs, Division of Investigation (DOI), Health Quality Investigation Unit.2 Also enclosed was a “Notice to Medical Consumers” (capitalization omitted) explaining that patient records reviewed in connection with DOI investigations “are kept confidential and no information about the patient’s care is disclosed to the general public . . . .” Although patient records could become part of the official record of a legal proceeding, “[e]ven then, efforts are made to protect the privacy and identity of the individual patients.” The six patients were advised that, if they exercised their “right not to consent to the release[,]” DOI would “take the necessary

2 The Board is a unit of the Department of Consumer Affairs. (See Bus. & Prof. Code, § 2001, subd. (a).)

3 steps to subpoena the . . . records.” The Board did not receive a signed authorization form from any of the six patients. In September 2016, an investigator issued investigational subpoenas duces tecum (the subpoenas) commanding Dr. Soorani to produce the following for each of the six patients: “A certified copy of the documentation supporting your rationale for the prescriptions you wrote for the patient . . . between the dates [June 1, 2012] through [September 12, 2016], including the different medications, doses, and refills. Documentation includes treatment notes that support the differential diagnosis for the medications, the treatment plan and orders, and all follow up including reviews of vital signs, patient complaints of side effects of medications, laboratory tests to ensure drug efficacy and to rule out drug toxicity, and physical examinations.” (Bolding omitted.) Each of the six patients was sent a copy of the subpoena seeking his or her records, as well as a notice advising of the right to object. Approximately one week later, Dr. Soorani’s attorney sent a letter to the Board’s investigator stating that the doctor would not produce the medical records sought by the subpoenas without patient authorization and invoking the psychotherapist-patient privilege (Evid. Code, § 1010 et seq.) and the right to privacy under article I, section 1 of the California Constitution. Dr. Soorani’s attorney enclosed letters from four of the six patients indicating that they did not authorize disclosure of their medical records. II. Petition to Compel Compliance with the Subpoenas In October 2017, more than a year after the deadline to comply with the subpoenas had passed, the director of the Department of Consumer Affairs petitioned the trial court for an

4 order requiring Dr. Soorani to produce the subpoenaed medical records. (Gov. Code, §§ 11186, 11187.) A. Dr. Klessig’s declaration In support of the petition, the Board submitted a declaration from Dr. Klessig, in which she opined that good cause existed to believe that Dr. Soorani violated the Medical Practice Act and “was practicing medicine outside the standard of care when he prescribed narcotics, sedative agents and other controlled substances to patients in large amounts.” Obtaining the medical records of the six patients was “[t]he only way to ascertain whether this is true . . . .” Dr. Klessig detailed the following prescribing irregularities regarding the six patients that she found in the CURES report. 1. Patient T.M. According to Dr. Klessig, Dr. Soorani excessively and erratically prescribed multiple stimulant and sedative medications to T.M. T.M. was prescribed Vyvanse, “an amphetamine-like stimulant” used to treat attention deficit hyperactivity disorder (ADHD). Although the maximum daily dose of Vyvanse is 60 to 70 milligrams, T.M. received 30, 60-milligram tablets, followed only 14 days later by another 30, 70-milligram tablets— effectively “twice the maximum safe dose.” The next month, T.M. “switched to amphetamine salts,” but several months later he was prescribed the maximum recommended doses of both Vyvanse and the amphetamine salts. T.M. was also prescribed a “very large” two-milligram dose of clonazepam, a sedative used to treat panic disorders and seizures—problems that “can be worsened by amphetamine use.”

5 He also received oxycodone and OxyContin—both “strong narcotics.” A few months later, T.M. was prescribed a transdermal fentanyl patch, “an extremely potent narcotic with a very high risk of unintentional death.” This drug “is only indicated when other means of pain management have failed[.]” On the same day, he received another prescription for oxycodone, which “in combination with the clonazepam was unsafe.” A month later, T.M. received a fentanyl refill and a new prescription for Subsys, another form of fentanyl. Although the recommended starting dose of Subsys is 100 micrograms, T.M. was given a 600-microgram dose. Several months later, T.M. was given 30 doses of 1,200 micrograms. “At the maximum safe dose, . . .

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Bluebook (online)
Grafilo v. Soorani, Counsel Stack Legal Research, https://law.counselstack.com/opinion/grafilo-v-soorani-calctapp-2019.