Cleeton v. SIU Healthcare, Inc.

2022 IL App (4th) 210284-U
Appellate Court of Illinois·Decided June 7, 2022·No. 4-21-0284·Unpublished·Cited by 1 cases

Opinion

NOTICE

2022 IL App (4th) 210284-U FILED

This Order was filed under June 2, 2022

Supreme Court Rule 23 and is not precedent except in the Carla Bender

NO. 4-21-0284 4th District Appellate limited circumstances allowed under Rule 23(e)(1). Court, IL IN THE APPELLATE COURT

OF ILLINOIS

FOURTH DISTRICT

CAROL CLEETON, as Independent Administrator of the ) Appeal from the Estate of Donald Cleeton, Deceased, ) Circuit Court of Plaintiff-Appellant, ) Sangamon County v. ) No. 19L32 SIU HEALTHCARE, INC.; CHARLENE YOUNG; )

ABDULLAH AL SAWAF; SIU PHYSICIANS & )

SURGEONS, INC., d/b/a SIU MEDICINE, an Illinois )

Corporation; STEPHANIE WHOOLEY; SUE FERRILL; )

ASHLEY KOCHMAN; and MEDTRONIC, INC., )

Defendants, )

and )

MEMORIAL MEDICAL CENTER; MOUHAMAD )

BAKIR; JESSICA FARLEY; NAUMAN JAHANGIR; )

HANNAH PURSEGLOVE; NATALIE MAHONEY; )

JONATHAN RODERICK DUTT; AND SHILPA )

CHAKU, )

Respondents in Discovery ) Honorable ) Raylene Grischow,

(Mouhamad Bakir, Appellee). ) Judge Presiding.

JUSTICE TURNER delivered the judgment of the court.

Justices DeArmond and Holder White concurred in the judgment.

ORDER

¶1 Held: The circuit court properly denied plaintiff’s motion to convert respondent in discovery, Dr. Mouhamed Bakir, to a defendant.

¶2 Plaintiff, Carol Cleeton, as the independent administrator of the estate of Donald Cleeton, deceased, appeals the Sangamon County circuit court’s May 3, 2021, order denying her motion to convert Dr. Mouhamad Bakir from a respondent in discovery to a defendant under section 2-402 of the Code of Civil Procedure (Procedure Code) (735 ILCS 5/2-402 (West 2018)).

The order also terminated Dr. Bakir’s status as a respondent in discovery. On appeal, plaintiff contends the circuit court erred by denying her motion to convert Dr. Bakir to a defendant because (1) it failed to apply the proper standard of probable cause; (2) it erred in finding plaintiff failed to establish the standard of care applicable to Dr. Bakir; (3) it exceeded its authority by determining decedent’s signs and symptoms were inconsistent with baclofen withdrawal syndrome; (4) it exceeded its authority by determining Dr. Bakir complied with the standard of care; and (5) the evidence supports the opinion of Dr. William Minore, plaintiff’s expert witness, decedent died from baclofen withdrawal syndrome. We affirm.

¶3 I. BACKGROUND

¶4 When he was 17 years old, decedent sustained a cervical cord injury that left him a quadriplegic. In December 2014, Dr. Jose Espinosa implanted a Medtronic SynchroMed II programmable pump in decedent to reduce the extent of involuntary muscle spasms decedent experienced. The pump delivered baclofen, which is also known as Lioresal Intrathecal, for spasticity control. After the implantation, decedent’s pump was managed by the Southern Illinois University (SIU) Department of Neurology, specifically defendant Charlene Young, a family nurse practitioner, and her clinic nurse, Ashley Kochman. Young and Kochman were employees of defendant SIU Healthcare, Inc.

¶5 On October 25, 2017, decedent, then 25 years old, presented with plaintiff, his mother, at the SIU Neurology clinic for a routine pump refill. Kochman and Young unsuccessfully attempted to refill decedent’s pump multiple times. Young was eventually able to refill decedent’s pump.

¶6 On October 29, 2017, around 8:15 p.m., decedent was brought by ambulance to the Memorial Medical Center emergency room because decedent was complaining of abdominal

pain and a headache following his pump refill. Decedent also noted increased spasms since the refill. He also recently had a urinary tract infection. Decedent was seen in the emergency room by Dr. Richard Austin. At 8:30 p.m., Dr. Austin consulted Dr. Nauman Jahangir, a neurology resident. The emergency room notes stated Dr. Jahangir recommended having a Medtronic representative interrogate the device. A Medtronic representative came to the emergency room and interrogated decedent’s pump. The interrogation showed no functional error with the pump. The emergency room notes for decedent contain diagnoses of sepsis and acute urinary tract infection. Dr. Austin admitted decedent to the hospital and transferred decedent’s care shortly before midnight. In transferring care of decedent, Dr. Austin spoke with Dr. Nichole Mirocha.

¶7 On October 30, 2017, Dr. Mirocha telephoned Dr. Bakir, a pulmonary critical care specialist, to have decedent transferred to the intensive care unit (ICU) to address tachycardia, altered mentation, and possible seizures. Dr. Mirocha provided Dr. Bakir with decedent’s history, including the interrogation of decedent’s baclofen pump in the emergency room. Decedent was transferred to the ICU around 10 a.m., and Dr. Bakir became decedent’s managing physician. Dr. Keivan Shalileh, a pulmonary medicine fellow, and Dr. Hannah Purseglove, a resident, were also working in the ICU that day. As a pulmonary critical care specialist, Dr. Bakir was aware of baclofen, but the baclofen pump was not part of his intensive care and pulmonology practice. Prior to October 30, 2017, Dr. Bakir had never had a patient who potentially was experiencing baclofen withdrawal syndrome. Dr. Bakir did a review of decedent’s chart, examined decedent, and spoke with plaintiff, who informed him of decedent’s difficult pump refill on October 25, 2017. Due to decedent’s heart rate, Dr. Bakir immediately consulted cardiology. Dr. Momin Siddique, a cardiologist, responded and ordered tests investigating a possible pulmonary embolism and decedent’s elevated troponin level. Dr. Bakir

also consulted neurology, neurosurgery, and the baclofen pump team.

¶8 At 10:44 a.m., a Medtronic employee faxed the emergency procedures for baclofen withdrawal to Memorial Medical Center (Medtronic emergency procedure documents), after receiving a request for troubleshooting assistance with decedent’s pump. The Medtronic emergency procedure documents were incorporated into Memorial Medical Center’s electronic medical records for decedent at 6:44 p.m. on October 30, 2017. In his deposition, Dr. Bakir testified the Medtronic emergency procedure documents were never provided to him while he was caring for decedent.

¶9 Around 11:15 a.m., Dr. Abdullah Al Sawaf, a neurologist, and Dr. Shilpa Chaku, a neurology resident, examined decedent. Dr. Al Sawaf’s differential diagnosis for decedent was “mild-moderate baclofen withdrawal vs sepsis (?urine source).” He noted decedent’s “[n]ormal tone argues against baclofen withdrawal, but the timeline of events and dysautonomia supports that possibility.” Dr. Al Sawaf further found sepsis could present similarly. He asked Young to interrogate decedent’s pump to rule out failure. Young did so and reported the pump was working as expected. Dr. Al Sawaf found decedent’s episodes in which his eyes would roll back and flutter were likely a dysautonomia phenomenon and not seizures. After Dr. Al Sawaf examined decedent, he and his team spoke with Dr. Bakir and the ICU team about decedent’s case. During the discussion, both Dr. Bakir and Dr. Al Sawaf indicated their lack of familiarity with baclofen withdrawal syndrome. Dr. Al Sawaf stated he did not think it was baclofen withdrawal syndrome because decedent’s tone was normal. No discussion took place about a possible pump catheter malfunction.

¶ 10 A code blue was called for decedent around 12:07 p.m. due to a lack of pulse. During the code, Dr. Espinosa recommended intrathecal administration of baclofen, which was

given by Dr. Todd Knox at 2:05 p.m. After three hours of resuscitation efforts, decedent was declared dead at 3:06 p.m. Later tests revealed the catheter for decedent’s pump had holes in it.

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