Mary Margaret Upchurch and Rickie Upchurch v. Adam I. Lewis, M.D. and Jackson Neurosurgery Clinic, PLLC

• Court: Court of Appeals of Mississippi
• Decided: September 23, 2025
• Docket: 2023-CA-01296-COA
• Status: Published

Opinion

IN THE COURT OF APPEALS OF THE STATE OF MISSISSIPPI

NO. 2023-CA-01296-COA

MARY MARGARET UPCHURCH AND RICKIE APPELLANTS UPCHURCH

v.

ADAM I. LEWIS, M.D. AND JACKSON APPELLEES NEUROSURGERY CLINIC, PLLC

DATE OF JUDGMENT: 07/12/2023 TRIAL JUDGE: HON. M. BRADLEY MILLS COURT FROM WHICH APPEALED: RANKIN COUNTY CIRCUIT COURT ATTORNEYS FOR APPELLANTS: JOSEPH E. ROBERTS JR. CRYMES MORGAN PITTMAN ANN RUSSELL CHANDLER ATTORNEYS FOR APPELLEES: L. CARL HAGWOOD DAVID MARK EATON NATURE OF THE CASE: CIVIL - MEDICAL MALPRACTICE DISPOSITION: REVERSED AND REMANDED - 09/23/2025 MOTION FOR REHEARING FILED:

CONSOLIDATED WITH

NO. 2024-CA-00396-COA

ADAM I. LEWIS, M.D. AND JACKSON APPELLANTS NEUROSURGERY CLINIC, PLLC

MARY MARGARET UPCHURCH AND RICKIE APPELLEES UPCHURCH

DATE OF JUDGMENT: 02/21/2024 TRIAL JUDGE: HON. M. BRADLEY MILLS COURT FROM WHICH APPEALED: RANKIN COUNTY CIRCUIT COURT ATTORNEYS FOR APPELLANTS: L. CARL HAGWOOD DAVID MARK EATON ATTORNEYS FOR APPELLEES: JOSEPH E. ROBERTS JR. CRYMES MORGAN PITTMAN ANN RUSSELL CHANDLER NATURE OF THE CASE: CIVIL - MEDICAL MALPRACTICE DISPOSITION: AFFIRMED - 09/23/2025 MOTION FOR REHEARING FILED:

BEFORE CARLTON, P.J., McCARTY AND WEDDLE, JJ.

WEDDLE, J., FOR THE COURT:

¶1. Mary Margaret Upchurch suffered paralysis in her legs following a surgery performed

at Merit Health Rankin by Dr. Adam Lewis, a neurosurgeon with Jackson Neurosurgery

Clinic PLLC (Jackson Neurosurgery). Mary and her husband, Rickie, filed a medical-

malpractice lawsuit in the Rankin County Circuit Court against multiple defendants,

including Dr. Lewis, Jackson Neurosurgery, and Merit Health Rankin. After settling their

claims against Merit Health Rankin, the Upchurches proceeded to trial against only Dr.

Lewis and Jackson Neurosurgery.

¶2. A Rankin County Circuit Court jury found that Dr. Lewis was not negligent in his care

and treatment of Mary and returned a verdict in favor of Dr. Lewis and Jackson

Neurosurgery. The circuit court entered a judgment on the verdict and dismissed with

prejudice all charges against Dr. Lewis and Jackson Neurosurgery. The circuit court

subsequently entered an order denying the Upchurches’ post-trial motion for judgment

notwithstanding the verdict (JNOV) or, alternatively, a new trial.

¶3. In appellate case number 2023-CA-01296-COA, the Upchurches appeal from the jury

verdict, the circuit court’s final judgment, and the circuit court’s order denying their post-trial

motions. The Upchurches argue that the circuit court erred by (1) failing to grant their

2 motion for a directed verdict as to the liability of Merit Health Rankin’s nursing staff; (2)

failing to grant their motion for JNOV or, alternatively, a new trial; and (3) improperly

instructing the jury.

¶4. After the Upchurches designated the record for appeal, Dr. Lewis and Jackson

Neurosurgery sought to include over forty additional documents in the appellate record. The

estimated costs of the appeal for the additional documents Dr. Lewis and Jackson

Neurosurgery sought to include exceeded $30,000. The Upchurches disputed the need for

all the documents and asked the circuit court to assess the costs of any additional appellate

record designations to Dr. Lewis and Jackson Neurosurgery. The circuit court granted the

Upchurches’ motion to assess the costs of the amended designation to Dr. Lewis and Jackson

Neurosurgery but also granted them leave to submit another amended designation of the

record for appeal if they wished to do so. In appellate case number 2024-CA-00396-COA,

Dr. Lewis and Jackson Neurosurgery appeal from the order assessing the costs of the

amended designation of the appellate record to them. Because the two appeals stem from the

same underlying matter, this Court has consolidated the appeals.

¶5. Upon reviewing the issues raised in appellate case number 2023-CA-01296-COA, we

find, in light of the substantial credible evidence the Upchurches presented through their fact

and expert witnesses, there was insufficient evidence to support the jury’s verdict in favor

of Dr. Lewis and Jackson Neurosurgery. Dr. Lewis’s own testimony constituted the only

evidence that the medical device he implanted during Mary’s surgery was compatible with

another manufacturer’s previously implanted medical device and that his decision to “mix

3 and match” different manufacturers’ medical equipment complied with the standard of care.

¶6. After reviewing the record, we cannot find that Dr. Lewis was ever tendered or

accepted as an expert witness, and any testimony he gave regarding the standard of care was

improperly admitted. Dr. Lewis was the sole witness to testify that mixing and matching

different manufacturers’ medical equipment complied with the standard of care. By contrast,

the Upchurches presented multiple expert witnesses who testified that performing Mary’s

surgery with only a different manufacturer’s medical device available breached the standard

of care. In light of this and the substantial evidence that the Upchurches provided as to the

standard of care and Dr. Lewis’s negligence in causing Mary’s injuries, we find that

insufficient evidence supported the jury’s verdict. As a result, we conclude that the circuit

court erred by denying the Upchurches’ post-trial motion for JNOV.

¶7. We therefore reverse the circuit court’s judgment and the jury’s verdict in favor of Dr.

Lewis and Jackson Neurosurgery and remand the case for a new trial. Because we find this

issue dispositive, we decline to address the Upchurches’ remaining arguments on appeal in

appellate case number 2023-CA-01296-COA. In appellate case number 2024-CA-00396-

COA, we find no error in the circuit court’s order assessing the costs of an amended

designated appellate record to Dr. Lewis and Jackson Neurosurgery. We therefore affirm the

circuit court’s order at issue in Dr. Lewis and Jackson Neurosurgery’s consolidated appeal.

FACTS

¶8. Mary suffered from severe fibromyalgia and chronic back pain. In 2009, she

underwent surgery to have a spinal cord stimulator manufactured by St. Jude Medical Inc.

4 (St. Jude)1 implanted to provide relief from the pain. The spinal cord stimulator was powered

by a battery that St. Jude also manufactured. The two system components were connected

by leads that ran from the spinal cord stimulator and plugged into the battery, also referred

to as an implantable pulse generator. To provide Mary with relief from her pain, the battery

was supposed to send an electrical current through the leads that connected to the spinal cord

stimulator. Unfortunately, the St. Jude spinal cord stimulator provided inadequate relief for

Mary’s back pain. As a result, in 2011, Mary underwent another procedure to have a pain

pump implanted. The pain pump delivered small doses of pain-relieving medicine directly

into Mary’s spinal cord, which finally began to provide her with adequate relief.

¶9. In 2014, the Upchurches moved to Mississippi. In September 2015, Mary had surgery

to replace the original St. Jude battery connected to her spinal cord stimulator with a new St.

Jude battery. At trial, Rickie testified that after the September 2015 surgery to replace the

original battery, the spinal cord stimulator finally began providing Mary with noticeable pain

relief. In the spring of 2016, the Upchurches learned during a visit to Mary’s doctor that her

pain pump would need to be replaced soon. Mary’s physician referred her to Dr. Lewis for

the replacement of the pain pump.

¶10. At trial, the Upchurches called Dr. Lewis to testify as an adverse fact witness during

their case-in-chief. Though he was never offered or accepted as an expert medical witness

in any field, Dr. Lewis testified about the care and treatment he provided to Mary. Dr. Lewis

1 Throughout the opinion, we refer to St. Jude Medical Inc. as “St. Jude” for readability and not to indicate any other entities, such as St. Jude Children’s Research Hospital.

5 stated that during his consultation with the Upchurches, he discussed replacing Mary’s

current pain pump with a pain pump manufactured by Boston Scientific. According to

Rickie’s testimony, although there were serious risks associated with replacing the pain

pump, Mary was willing to undergo the procedure due to the significant benefits and relief

she received from the pain pump. During the consultation, Dr. Lewis also asked the

Upchurches about Mary’s St. Jude spinal cord stimulator. Rickie testified that he and Mary

told Dr. Lewis that they felt the St. Jude stimulator system was working well and providing

Mary with fairly consistent pain relief after the surgery several months earlier to replace the

battery. The Upchurches explained that their only complaint with the St. Jude system was

that the battery seemed to take a long time to charge.

¶11. Even though the Upchurches expressed an overall satisfaction with Mary’s St. Jude

system, Dr. Lewis testified that he recommended Mary switch to the spinal cord stimulator

manufactured by Boston Scientific. Although Dr. Lewis stated that Todd Dyess, a Boston

Scientific sales representative, joined in his consultation with the Upchurches, Dyess later

testified that he had no recollection of any consultation with Dr. Lewis and the Upchurches.

Regardless of Dyess’s presence or absence at the consultation, Dr. Lewis stated that he

recommended to the Upchurches that Boston Scientific’s spinal cord stimulator would be an

upgrade to Mary’s current St. Jude model. Dr. Lewis explained that the Boston Scientific

spinal cord stimulator only took fifteen minutes to charge and could be programmed to

provide different types of stimulation to help reduce Mary’s pain.

¶12. In contrast to Dr. Lewis’s testimony about the consultation, Rickie stated that his and

6 Mary’s discussions with Dr. Lewis remained limited to the replacement of Mary’s pain pump

and her St. Jude battery. Rickie testified that they never discussed with Dr. Lewis replacing

Mary’s spinal cord stimulator or the leads that connected the spinal cord stimulator to the

battery. In fact, Rickie testified that Dr. Lewis repeatedly assured the Upchurches the leads

from Mary’s St. Jude spinal cord stimulator would fit into the Boston Scientific Precision

Spectra battery that he recommended to them. Rickie stated that even if the topic of

replacing the leads or the stimulator had come up, he and Mary never would have consented

to those procedures. Rickie explained that he and Mary felt the risks associated with

replacing the leads or the stimulator outweighed any potential benefits of the procedures. As

Rickie testified, “[Mary] already had significant benefit from the pain pump[,]” which they

consented to replace despite the associated risks, and therefore, “[t]here was no reason in our

minds to [also] accept the greater risks of moving the leads in her spine.”

¶13. On June 15, 2016, Dr. Lewis performed Mary’s surgery. Dr. Lewis removed Mary’s

St. Jude battery and replaced it with the Boston Scientific Precision Spectra battery. He then

successfully connected the first lead from Mary’s St. Jude spinal cord stimulator to the new

battery. Dr. Lewis testified, however, that the second lead would not fit properly into the

new battery. At various points throughout his testimony, Dr. Lewis described the second lead

as irregularly shaped, bent, flimsy, and corroded. After he was unable to connect the second

lead to the Boston Scientific battery, Dr. Lewis testified that someone was sent to Rickie in

the waiting room to ask if Rickie wanted to stop Mary’s procedure or give additional consent

for the replacement of her spinal cord stimulator.

7 ¶14. The jury heard contradictory testimony as to what occurred when the hospital

employee spoke to Rickie in the waiting room. According to Dr. Lewis, Rickie’s informed

consent was obtained to replace Mary’s spinal cord stimulator. As a result, Dr. Lewis

testified that he performed a laminectomy on Mary, which required him to remove a portion

of Mary’s spinal bone to access her spinal canal. Dr. Lewis stated that he then replaced

Mary’s existing St. Jude stimulator with a Boston Scientific stimulator and completed the

surgery.

¶15. Rickie confirmed that a hospital employee approached him in the waiting room and

informed him that there had been a problem fitting Mary’s St. Jude stimulator leads into the

new Boston Scientific battery. Rickie stated that the employee asked if Rickie wanted Dr.

Lewis “to put the leads in or . . . put in the new battery and . . . do whatever or just quit[.]”

Rickie repeatedly testified that the employee never informed him that continuing surgery

meant exposing Mary to greater risks by performing a laminectomy to replace Mary’s current

leads with more invasive paddles. Rickie also testified that the employee never specifically

discussed with him that replacing the leads to Mary’s spinal cord stimulator with paddles

posed the risk of paralysis.

¶16. Rickie stated that he never received a phone call from either Dr. Lewis or his assistant

regarding the progress or outcome of Mary’s surgery. In the afternoon, hospital personnel

escorted Rickie to the post-anesthesia care unit (PACU), where Mary was recovering. Rickie

testified that Mary’s post-surgery recovery differed from her prior surgical experiences.

Rickie explained that Mary woke up slowly and was “in a lot of pain[,]” which “usually

8 [was] not the case” after surgery. Rickie stated that he remained with Mary in the PACU and

once she was transferred to her own hospital room.

¶17. After Mary was moved to a room, Rickie testified that she began to complain of

numbness in her legs, particularly her left leg. A friend came to stay with Mary while Rickie

left for about an hour. Rickie testified that upon returning to the hospital, he remained with

Mary in her room until about 11:30 p.m. Rickie stated that although he had seen Dr. Lewis

before Mary’s procedure, he (Rickie) had no further communication with or contact from Dr.

Lewis on the day of Mary’s procedure.

¶18. For his part, Dr. Lewis testified that after Mary’s surgery, he examined her in the

PACU and entered a post-operative note around 5 p.m. to document his findings. Like

Rickie, Dr. Lewis observed that Mary was slow to wake up from her surgery. Dr. Lewis also

observed that Mary had a little weakness in her left leg and a little numbness below her left

knee and in her left foot. Dr. Lewis acknowledged that “the first signs [of a hematoma, or

a blood clot,] are numbness followed by weakness.” Dr. Lewis explained that “when

someone develops a hematoma in the spinal cord, it’s not usually one sided.” Rather, both

sides of the body are affected. Dr. Lewis stated that when a hematoma forms after spinal

surgery, the symptoms generally begin “with burning intense pain down the leg [that]

progresses to . . . dense numbness, and then it goes to paralysis on both sides.” Dr. Lewis

maintained that when he examined Mary in the PACU, he only observed slight weakness and

numbness on one side of her lower body. He explained that Mary’s symptoms did not overly

concern him at that time since he had just operated on the left side of her spinal cord. Dr.

9 Lewis further explained that he expected any issues Mary was experiencing to resolve within

the next twenty-four hours.

¶19. Janet Bullock, who worked as the primary nurse on the surgical recovery floor at the

time of Mary’s transfer, testified that Mary arrived on her floor around 4:30 p.m. Around 5

p.m., Nurse Bullock entered a note stating that Mary could not move her left leg. Nurse

Bullock’s note further stated that although Mary had minimal movement in her right toes,

Mary complained of numbness in both her right lower leg and foot. Nurse Bullock testified

that Mary’s condition “was highly irregular” and concerning. As a result, Nurse Bullock

called Dr. Lewis to report her observations and ask what steps he wanted her to take with

regard to Mary’s care. During their telephone conversation, Dr. Lewis told Nurse Bullock

to give Mary a steroid shot. Nurse Bullock evaluated Mary again around 6:30 p.m. and

found that Mary’s condition did not appear to have changed or improved after the steroid

shot. At 7 p.m., Nurse Bullock finished her shift, and another nurse took over Mary’s care

and supervision.

¶20. Dr. Lewis testified that on the morning after Mary’s surgery, he reexamined Mary

around 7:15 a.m. At that time, Dr. Lewis noted that Mary’s condition had worsened and that

she was very weak in both legs. Based on his concern that Mary had developed a hematoma,

Dr. Lewis took Mary back to surgery. Upon questioning, Dr. Lewis maintained that his

findings when he examined Mary in the PACU had differed from the observations that Nurse

Bullock made. Dr. Lewis stated that if he had observed paralysis on Mary’s entire lower left

side as Nurse Bullock’s note had indicated, he either would have ordered a CAT scan or

10 taken Mary immediately back to surgery. Dr. Lewis testified that Mary’s hematoma

presented not as an immediate post-surgical complication but rather appeared to have

developed gradually overnight.

¶21. During Mary’s second surgery, Dr. Lewis discovered a large hematoma pressing down

on her spinal cord. Dr. Lewis also discovered that Mary “had bleeding from every incision.”

Dr. Lewis stated that “[s]omething had happened where she had had some kind of reaction

either to the anesthesia or medication that caused every incision in her body, from the pain

pump, even the tract to connect the leads, . . . was bleeding and oozing.” Dr. Lewis removed

the blood clot and explored Mary’s incisions. Dr. Lewis testified that although he consulted

with both a hospitalist and a hematologist, they were unable to determine what caused Mary’s

surgical incisions to bleed.

¶22. Dr. Lewis stated that Mary initially seemed to improve after he removed the

hematoma, but then her weakness eventually returned and increased. Due to Mary’s renewed

weakness and the bleeding around her incisions, Dr. Lewis took her to surgery for a third

time. During the third surgery, Dr. Lewis did not find another hematoma or any other cause

of Mary’s weakness, and he attributed her condition to post-surgical swelling around her

spinal cord.

¶23. The paralysis in Mary’s legs failed to improve. In August 2018, the Upchurches filed

a medical-malpractice lawsuit against Dr. Lewis, Jackson Neurosurgery, and Merit Health

Rankin. Prior to trial, the Upchurches settled their claims involving Merit Health Rankin.

¶24. The Upchurches designated Dr. Narlin Beaty as an expert in not only general

11 neurosurgery but also the implantation, removal, and replacement of spinal cord stimulators,

batteries, and leads. With no objection from Dr. Lewis, the circuit court accepted Dr. Beaty

as an expert witness in these areas. Dr. Beaty testified that he practiced as a neurosurgeon

and was familiar with spinal cord stimulators manufactured by Boston Scientific, St. Jude,

and Medtronic. Dr. Beaty stated that he regularly performed surgeries that involved

implanting, removing, and replacing these models and their batteries. Dr. Beaty also stated

that he was familiar with the standard of care that existed in 2016 with regard to not only

performing but also obtaining consent for the implantation of spinal cord stimulators,

batteries, and leads.

¶25. During his testimony, Dr. Beaty discussed Dr. Lewis’s characterization of Mary’s St.

Jude leads as “corroded.” Dr. Beaty testified that although he had “seen lots of leads” during

his practice, he had “never seen . . . rust or iron oxidation on a lead.” Dr. Beaty explained

that the leads “live in fat” inside the human body, “and generally[,] if you want to keep a

piece of metal intact, you . . . oil it. You put oil on it, and so the fat from the human [body’s]

oil usually keeps them intact.” In addition, Dr. Beaty noted that just nine months before Dr.

Lewis operated on Mary, another surgeon had replaced Mary’s St. Jude battery. Dr. Beaty

testified that nothing from the prior surgeon’s notes indicated there had been an issue with

the condition of Mary’s St. Jude leads at that time.

¶26. In Dr. Beaty’s expert opinion, Dr. Lewis deviated from the standard of care owed to

Mary in three ways. Specifically, Dr. Beaty stated that Dr. Lewis failed to be properly

prepared for surgery, obtain proper informed consent for surgery, and properly communicate

12 with Merit Health Rankin’s nursing staff after Mary’s surgery. With regard to Dr. Lewis’s

preparedness for surgery, Dr. Beaty testified that Dr. Lewis should have ensured that a St.

Jude representative was present and that the proper medical equipment was available when

he began Mary’s surgery. Dr. Beaty stated, “[T]he bottom line is, it’s the surgeon’s

responsibility to ensure that the operating room, a representative[,] and all pieces along the

chain are functional and that the equipment is present in order to provide surgery.”

¶27. Dr. Beaty testified that a Boston Scientific adapter, known as the Precision S8 adapter,

existed “to connect existing leads that otherwise do not fit . . . to the Boston Scientific

[Precision Spectra] battery” and “to fix the problem that . . . Mrs. Upchurch and Dr. Lewis

had . . . that day.” Further testimony presented at trial reflected that Boston Scientific

designed its Precision S8 adapter to connect the Precision Spectra battery with stimulator

leads designed by other manufacturers, such as St. Jude. Even though Dr. Lewis offered

testimony to contest whether Boston Scientific’s Precision S8 adapter was available at the

time he performed Mary’s surgery, Dr. Beaty stated that the adapter’s availability did not

alter his opinion that Dr. Lewis deviated from the standard of care. Dr. Beaty testified that

he knew of no way to make Boston Scientific’s Precision Spectra battery compatible with St.

Jude leads without an adapter. Dr. Beaty further opined that trying to connect a Boston

Scientific battery to St. Jude leads was not only outside the directions-of-use information that

Boston Scientific provided for its Precision Spectra battery but also fell below the standard

of care. Dr. Beaty reiterated that the standard of care additionally required Dr. Lewis to have

a St. Jude medical-device sales representative present for Mary’s surgery so that the

13 representative could assist with any equipment-related issues that arose.

¶28. Dr. Beaty concluded that Dr. Lewis “ended up doing more surgery because he was not

prepared for the planned surgery[,] and unfortunately for Mrs. Upchurch[,] that additional

surgery cost her a great deal of neurological function and changed the quality of her life.”

He stated that if Dr. Lewis “had the appropriate battery, then the additional surgery would

not have been necessary[,] and the complication would not have happened.” In addition to

the mid-surgery complication, Dr. Beaty concluded that the initial surgery Dr. Lewis

performed “caused compression of [Mary’s] spinal cord” and “a hematoma[,] which . . . then

[had to be] evacuated the following morning.”

¶29. Dr. Beaty also testified regarding the ways he believed Dr. Lewis deviated from the

standard of care in obtaining informed consent prior to Mary’s surgery, handling the mid-

surgery complication that arose, and communicating with Merit Health Rankin’s nursing staff

after surgery. Dr. Beaty stated Dr. Lewis’s post-operative note demonstrated that Mary had

“a small but present neurologic deficit[,]” and several notes from the nursing staff

“document[ed] a large neurologic deficit.” Dr. Beaty testified that other than ordering

steroids for Mary, which was inadequate, no other steps were taken to address the neurologic

deficit. According to Dr. Beaty, the communication failure between Dr. Lewis and the

nursing staff also led to Mary’s poor outcome after surgery.

¶30. In addition to Dr. Beaty, the Upchurches designated Dr. Stephen Bloomfield, a

neurosurgeon and academic professor, as a second expert witness in the implantation and

replacement of spinal cord stimulators, leads, and batteries. Again, without any objection

14 from Dr. Lewis, the circuit court accepted Dr. Bloomfield as an expert witness in these

designated fields. Like Dr. Beaty, Dr. Bloomfield opined that Dr. Lewis deviated from the

standard of care and failed to appropriately prepare for surgery when he operated on Mary

without having the Boston Scientific Precision S8 adapter available. According to Dr.

Bloomfield:

[t]he standard of care would have dictated that the contact points needed to be tested with a proper system. And if [Dr. Lewis] did not prepare that proper system by [having] an S8 adapter prior to the separation, then he would have had to close the operation and then make plans to get that adapter to be able to perform that function.

An alternative would have been for him to use the old battery that he was removing to test this[,] but he would have required the programmer from the old battery company from St. Jude[,] and he did not have that presence. So he would need to connect the old battery again and then run those diagnostics to see whether or not the electrode needed to be fixed or not.

¶31. Dr. Bloomfield further agreed with Dr. Beaty’s opinion that Dr. Lewis deviated from

the standard of care after examining Mary in the PACU following her initial surgery. Dr.

Bloomfield stated that based on Dr. Lewis’s post-operative progress note, “there was a

significant suspicion that [Mary] was experiencing a compromise in function of her spinal

cord into the thoracic spine.” Dr. Bloomfield explained, “Dr. Lewis had come to see [Mary]

because of that suspicion. He examined her, found some findings that were abnormal[,] and

then placed her on steroids . . . in the effort to reduce the irritation of the spinal cord hoping

that that would help her spinal cord function recover.” Dr. Bloomfield testified, however,

that the standard of care requires “that whenever a patient has a new neurological problem

after surgery that can only be explained as a possible complication of the surgery[,] then an

15 imaging study is necessary emergently . . . to prove if there is pressure against the spinal cord

as she did have later on the next day.” Dr. Bloomfield stated that taking such measures

would give a patient who experienced pressure to his or her spinal cord the best chance for

recovery.

¶32. On cross-examination, Dr. Bloomfield again testified that the St. Jude leads were

incompatible with the Boston Scientific Precision Spectra battery. Although Dyess, Boston

Scientific’s sales representative, had stated that he did not know if the Precision S8 adapter

was available at the time of Mary’s surgery, Dr. Bloomfield explained “that if the S8 adapter

was requested prior to the surgery[,] it would have been made available.” And like Dr.

Beaty, Dr. Bloomfield opined that “[i]f the S8 adapter was not available despite asking for

it to begin with, then it would be a violation of the standard of care to try to place the St. Jude

electrodes into a Boston Scientific battery that was not compatible with those leads.”

¶33. The Upchurches also called Dyess as a fact witness during their case-in-chief. At the

time of Mary’s surgery, Dyess worked as a Boston Scientific medical-device sales

representative, and his sales territory included Mississippi. Dyess stated that in June 2016,

he had not been trained on and was not familiar with the Boston Scientific Precision S8

adapter. Dyess testified, however, that he never made off-label recommendations or those

not approved by the Federal Drug Administration to doctors and patients. As a result, Dyess

specifically denied ever representing to patients or physicians that a Boston Scientific battery

would be compatible with St. Jude leads.

¶34. Although Dyess was present during Mary’s surgery, he refuted Dr. Lewis’s earlier

16 testimony that he (Dyess) had been present during the pre-surgical consultation between Dr.

Lewis and the Upchurches. Because he was present during Mary’s surgery, Dyess knew that

Dr. Lewis had trouble fitting one of Mary’s St. Jude leads into the Boston Scientific battery.

Dyess stated, though, that he was not close enough to the operating table to clearly see the

reason for the difficulty. Dyess testified that from his vantage point, one of Mary’s leads

appeared to fit into the Boston Scientific battery, while the other lead only partially fit into

the new battery. Dyess stated that to the best of his knowledge, he did not remember seeing

a corroded lead as Dr. Lewis had earlier testified.

¶35. By agreement, the parties played for the jury the videotaped deposition of Ranjan

Nageri, who served as Boston Scientific’s designated corporate representative under

Mississippi Rule of Civil Procedure 30(b)(6). Nageri stated that he had worked at Boston

Scientific for thirteen years, had an engineering background, held patents on several medical

devices related to neurostimulation, and was familiar with the spinal cord stimulator systems

that Boston Scientific manufactured and sold. Nageri testified that he was also familiar with

the directions-for-use booklet that Boston Scientific had published on its Precision Spectra

system. The Upchurches entered the Precision Spectra’s directions-for-use booklet into

evidence as an exhibit during Nageri’s testimony. Boston Scientific’s directions-for-use

booklet on the Precision Spectra system reflected a copyright date of 2015, which was over

a year prior to the June 15, 2016 surgery that Dr. Lewis performed to connect Mary’s St. Jude

leads to the Precision Spectra battery.

¶36. During his video deposition, Nageri explained that the “Compatible Leads” section

17 of the directions-for-use booklet listed all the leads that Boston Scientific had tested and

determined to be compatible with the Precision Spectra battery. Nageri confirmed that

Boston Scientific designed and manufactured all the listed compatible leads. He further

confirmed that Boston Scientific did not design the Precision Spectra system to be

compatible with leads other than those specifically identified and that an adapter was

required to make the Precision Spectra battery compatible with leads manufactured by St.

Jude, Abbott, or Medtronic. Nageri stated that Boston Scientific designed the Precision S8

adapter to make its Precision Spectra battery compatible with St. Jude and Abbott leads.

Similarly, Boston Scientific designed the Precision M8 adapter to make its battery compatible

with Medtronic leads. According to Nageri, Boston Scientific had determined after

conducting research analysis that the leads had “different dimensional characteristics, . . . and

for them to be suitably mechanically and electrically compatible with [the battery], we would

need an adapter.” Nageri stated that he was uncertain when Boston Scientific’s Precision S8

adapter had become available for use.

¶37. The parties (also by agreement) played the video deposition of Dr. Lewis’s designated

expert neurosurgery witness, Dr. Warren Neely. Dr. Neely represented that he was familiar

with spinal cord stimulators, batteries, and pain pumps as well as the procedures related to

those devices’ implantation, replacement, and removal. He acknowledged, however, that

about twenty years had elapsed since he last participated in a procedure involving the

implantation of a spinal cord stimulator or battery. He further acknowledged that he had only

assisted in the implantation of the spinal cord stimulator’s paddles and not the implantation

18 of the spinal cord stimulator itself. Dr. Neely explained that because he did not perform such

surgeries directly, he referred patients needing spinal cord stimulators or batteries to other

physicians. Based on Dr. Neely’s lack of personal experience with the implantation of spinal

cord stimulators and batteries, the circuit court only allowed him to testify as an expert in

general neurosurgery.

¶38. Dr. Neely opined that Dr. Lewis did not breach the standard of care owed to Mary in

obtaining consent for and performing her surgery on June 15, 2016. Dr. Neely further opined

that Dr. Lewis complied with the appropriate standard of care in his diagnosis and treatment

of Mary after her initial surgery. Dr. Neely testified that a hematoma was a known risk of

spinal surgery and that the development of one after Mary’s surgery did not necessarily

indicate that Dr. Lewis had breached the standard of care.

¶39. On cross-examination, Dr. Neely acknowledged that Mary had her St. Jude battery

replaced in September 2015 without any compatibility issues arising. He further

acknowledged that Mary’s medical records indicated she was being referred to Dr. Lewis for

the replacement of her pain pump. Dr. Neely agreed that if Dr. Lewis failed to explain to the

Upchurches before surgery that Mary’s leads might also need to be replaced during surgery,

then that omission would have resulted in a deviation from the standard of care. In addition,

Dr. Neely admitted that he had seen no consent form in his review of Mary’s medical

documents that specifically discussed the possibility of needing to replace Mary’s leads

during surgery.

¶40. In response to further questioning, Dr. Neely agreed that Dr. Lewis’s own notes about

19 his pre-surgical consultation with the Upchurches appeared to indicate that Dr. Lewis was

unsure if Mary’s St. Jude leads would be compatible with the Boston Scientific Precision

Spectra battery. While reiterating that he did not perform the type of surgery that Mary

underwent, Dr. Neely acknowledged that not knowing before surgery if two types of systems

are compatible “[c]ould be” a deviation from the standard of care for performing surgery.

¶41. After considering all the parties’ testimony and evidence, the jury returned a verdict

in favor of Dr. Lewis and Jackson Neurosurgery and found that Dr. Lewis was not negligent

in his care and treatment of Mary. The circuit court denied the Upchurches’ post-trial motion

for JNOV or, alternatively, a new trial. Aggrieved, the Upchurches appealed from the jury’s

verdict and the circuit court’s order denying their post-trial motions. After the Upchurches

designated their appellate record, Dr. Lewis and Jackson Neurosurgery sought to amend the

designation to include over forty additional documents. The estimated costs of the amended

record designation requested by Dr. Lewis and Jackson Neurosurgery exceeded $30,000.

The circuit court granted the Upchurches’ request to assess the cost of an amended

designation to Dr. Lewis and Jackson Neurosurgery but also granted Dr. Lewis and Jackson

Neurosurgery leave to file another amended designation if they so chose. Aggrieved by the

circuit court’s order assessing the costs of the amended designation to them, Dr. Lewis and

Jackson Neurosurgery also appealed. Because the two appeals stem from the same

underlying matter, we consolidated them.

DISCUSSION

I. The Upchurches’ Appeal

20 ¶42. At trial, Dr. Lewis was the only witness to testify that mixing and matching different

manufacturers’ medical equipment did not breach the standard of care. By contrast, the

Upchurches presented substantial expert testimony to establish that Dr. Lewis’s failure to use

compatible medical equipment was one way in which he breached the standard of care and

that his negligent care and treatment caused Mary’s injuries. As a result, the Upchurches

contend that legally insufficient evidence supported the jury’s verdict finding Dr. Lewis was

not negligent, and they challenge the circuit court’s denial of their post-trial motion for

JNOV.

¶43. Relevant to the Upchurches’ argument, this Court has previously recognized that

[a] motion for JNOV challenges the legal sufficiency of the evidence, and its grant or denial is reviewed de novo. The appellate court will affirm the denial of a JNOV motion if there is substantial evidence to support the verdict. Substantial evidence is evidence of such quality and weight that reasonable and fair-minded men in the exercise of impartial judgment might reach different conclusions. The evidence will be considered in the light most favorable to the appellee, giving the party the benefit of all favorable inferences that may be reasonably drawn from the evidence.

Weaver v. Ross, 391 So. 3d 1240, 1247 (¶21) (Miss. Ct. App. 2024) (citations and internal

quotation marks omitted).

¶44. “A physician is under a duty to meet the national standard of care.” Est. of Northrop

v. Hutto, 9 So. 3d 381, 384 (¶9) (Miss. 2009). “The standard articulated must be objective,

not subjective.” Id. Thus, an expert’s “personal preference does not establish a national

standard of care.” Id. at 387 (¶13). In addition, Mississippi caselaw holds

that a physician can testify without being accepted as an expert regarding: (1) the facts and circumstances surrounding the care and treatment of the patient; (2) what his records about the patient reveal; and (3) what conditions the

21 patient was suffering from if the opinion was acquired during the care and treatment of the patient. However, the [Mississippi S]upreme [C]ourt [has] cautioned that a physician cannot testify about the significance of a patient’s condition or industry standards without first being accepted as an expert. We review a trial court’s admission of testimony for an abuse of discretion.

Kronfol v. Johnson, 283 So. 3d 1162, 1178 (¶38) (Miss. Ct. App. 2019) (citations and

internal quotation marks omitted). An error in admitting or excluding evidence “is

prejudicial, and ground for reversal, only when it affects the final result of the case and works

adversely to a substantial right of the party assigning it” as error. Bell v. State, 287 So. 3d

944, 961 (¶53) (Miss. Ct. App. 2019) (quoting Gray v. State, 799 So. 2d 53, 61 (¶30) (Miss.

2001)).

¶45. Here, the Upchurches indicated in the parties’ pretrial order that they might call Dr.

Lewis as a fact witness, and Dr. Lewis’s attorneys indicated that they planned to call him as

a fact and expert witness. However, the pretrial order constituted neither an acceptance by

the circuit court nor a designation by Dr. Lewis’s attorneys that Dr. Lewis was indeed an

expert witness. In fact, as the dissent acknowledges, the appellate record contains no filing

that actually designated Dr. Lewis as an expert witness.2 See post at (¶58) & n.4. And

2 In previously discussing the importance of properly designating expert witnesses for trial, we explained that

Rule 4.04(A) of the Uniform Rules of Circuit and County Court states: “Absent special circumstances the court will not allow testimony at trial of an expert witness who was not designated as an expert witness to all attorneys of record at least sixty days before trial.” “While the end result . . . may appear to be harsh, litigants must understand that there is an obligation to timely comply with the orders of our trial courts.” Bowie [v. Montfort Jones Mem’l Hosp.], 861 So. 2d [1037,] 1043 (¶16) [(Miss. 2003)]. As the circuit judge in this case expressed: “The Mississippi Rules of Civil Procedure are not advisory, and this Court’s Orders are not advisory.”

22 appellate courts cannot consider facts not in evidence or assume that certain evidence exists

simply because one party proclaims it to be so. See Rogers v. State, 318 So. 3d 1192, 1196

(¶15) (Miss. Ct. App. 2023).

¶46. Although the Upchurches called Dr. Lewis at the start of their case-in-chief, they did

so to elicit factual testimony about his care and treatment of Mary. Importantly, at no time

during Dr. Lewis’s initial questioning by the Upchurches’ attorney or during the subsequent

direct examination conducted by his own attorney was Dr. Lewis ever tendered as an expert

witness by one of the parties or accepted as an expert witness by the circuit court. Even so,

at one point during Dr. Lewis’s direct examination, his attorney asked if Dr. Lewis had

complied with the overall standard of care in treating Mary and, more specifically, if Dr.

Lewis had conformed with the standard of care with regard to the medical equipment he had

available for Mary’s surgery. Dr. Lewis’s attorney then began to ask about Dr. Lewis’s own

personal experiences and success in performing prior surgeries similar to Mary’s procedure.

¶47. As previously discussed, after reviewing the record, we cannot find where Dr. Lewis

was ever designated or accepted as an expert witness who was permitted to testify beyond

the actions he took and the observations he made during his care and treatment of Mary. See

Kronfol, 283 So. 3d at 1178 (¶38). The inclusion of Dr. Lewis’s name on the pretrial order

as a fact and expert witness whom his attorneys planned to call cannot overcome these

omissions and validate his inadmissible testimony. We therefore conclude that any expert

witness testimony Dr. Lewis provided as to the applicable standard of care was improper.

Buckley v. Singing River Hosp., 146 So. 3d 365, 373-74 (¶25) (Miss. Ct. App. 2013).

23 Moreover, as discussed, even a properly accepted expert witness may “not establish [the]

national standard of care” through his own personal preferences and experiences. Est. of

Northrop, 9 So. 3d at 387 (¶13). In addition, we conclude that the improper admission of Dr.

Lewis’s expert testimony adversely affected not only “a substantial right” of the Upchurches

but also “the final result of the case . . . .” Bell, 287 So. 3d at 961 (¶53).

¶48. While the dissent contends that the Upchurches failed to assert any error pertaining

to Dr. Lewis’s improperly admitted expert testimony, the matter is actually raised within their

very first issue. As phrased in the Upchurches’ appellate brief, “The Expert, Factual, and

Physical Evidence Overwhelmingly Proved” that the Boston Scientific device Dr. Lewis used

was incompatible with Mary’s preexisting St. Jude device. As part of their appellate

argument, the Upchurches included a chart to establish the lack of expert proof from Dr.

Lewis and the substantial expert proof they provided. In addition, the Upchurches repeatedly

assert on appeal that “Dr. Lewis failed to present competent factual or expert testimony” at

trial. We therefore find this issue was not only thoroughly briefed in written submissions but

also raised during oral argument before this Court.

¶49. As the Upchurches contend, other than Dr. Lewis’s own self-serving statements

regarding his compliance with the applicable standard of care, he presented only the

testimony of Dr. Neely for the jury’s consideration. Although Dr. Neely initially opined that

Dr. Lewis complied with the applicable standard of care in treating Mary, he later

acknowledged that he did not perform the type of surgery Mary had and that not knowing

whether two types of systems are compatible before starting surgery “[c]ould be” a deviation

24 from the standard of care. Dr. Neely also acknowledged that Dr. Lewis’s own pre-surgical

note about his consultation with the Upchurches seemed to indicate that Dr. Lewis was

unsure if Mary’s St. Jude leads would be compatible with the Boston Scientific Precision

Spectra battery.

¶50. In contrast to Dr. Lewis’s evidence, the Upchurches elicited testimony from Dyess,

a Boston Scientific medical-device sales representative, who stated that he never

recommended using a Boston Scientific battery with other manufacturers’ equipment to any

patients or physicians. The Upchurches also called Boston Scientific’s designated corporate

representative, Nageri, who repeatedly testified that an adapter was needed to connect the

Boston Scientific Precision Spectra battery to Mary’s existing St. Jude leads. Finally, the

Upchurches presented two expert neurosurgeons, who not only testified that an adapter was

necessary to successfully connect Mary’s existing St. Jude equipment to the new Boston

Scientific battery, but also that Dr. Lewis’s decision to begin Mary’s surgery without the

proper equipment available breached the standard of care. Furthermore, the Upchurches’

expert medical witnesses testified that Dr. Lewis’s negligence in treating and caring for Mary

resulted in the injuries she experienced.

¶51. Generally, when the issue on appeal involves nothing more than a battle of conflicting

expert testimony, the appellate courts will decline to reverse a fact finder’s determinations

as to the weight and credibility to be assigned to each expert’s testimony. See Univ. of Miss.

Med’l Ctr. v. Redd, 412 So. 3d 341, 355-56 (¶¶41-42) (Miss. Ct. App. 2024). After viewing

the evidence in the light most favorable to Dr. Lewis and Jackson Neurosurgery, though, we

25 cannot find that any credible, properly admitted evidence contradicted the Upchurches’

substantial fact and expert testimony showing that Dr. Lewis operated on Mary without the

appropriate medical equipment available to him and that this decision not only breached the

standard of care he owed to Mary but also caused her injuries. As a result, we conclude that

no legally sufficient evidence could support the jury’s verdict finding Dr. Lewis was not

negligent. We therefore reverse the circuit court’s order denying the Upchurches’ motion

that they were entitled to JNOV due to the insufficiency of the evidence supporting the

verdict.

¶52. In reversing a decision due to the legal insufficiency of the evidence, we often render

a verdict in favor of the party seeking judgment as a matter of law. See Est. of Walker v.

Hall, 331 So. 3d 553, 565 (¶38) (Miss. Ct. App. 2021). “[W]e also have the authority to

remand the case to the trial court” for a new trial. Id. at (¶¶38-39). Upon consideration, we

find the latter avenue more appropriate, and we therefore reverse and remand this case for

a new trial consistent with this opinion.

II. Dr. Lewis and Jackson Neurosurgery’s Appeal

¶53. In their consolidated appeal, Dr. Lewis and Jackson Neurosurgery contend that they

were permitted to designate additional documents for inclusion in the appellate record and

that the circuit court should have assessed the costs of the amended record designations to

the Upchurches. Dr. Lewis and Jackson Neurosurgery assert that the circuit court erred by

assessing the costs for their amended appellate record designations to them rather than to the

Upchurches. We review an “order to pay for the supplemental record . . . for abuse of

26 discretion.” In re City of Oxford, 142 So. 3d 401, 404 (¶11) (Miss. 2014).

¶54. “Mississippi Rule of Appellate Procedure 10 requires the appellant to designate the

portion of the record he or she finds relevant and necessary[,] and, if the appellee feels

additional portions of the record should be included, he or she may designate those.” Id. at

407 (¶20); see also M.R.A.P. 10 cmt. (stating that “[t]he purpose of the Rule is to permit and

encourage parties to include in the record on appeal only those matters material to the issues

on appeal”). “The clerk and reporter shall prepare the additional parts at the expense of the

appellant unless the appellant obtains from the trial court an order requiring the appellee to

pay the expense.” M.R.A.P. 10(b)(4).

¶55. As discussed, Dr. Lewis and Jackson Neurosurgery sought to include over forty

additional documents in the appellate record, and the estimated costs of the designations

exceeded $30,000. In light of the deferential standard of review we apply to this issue, we

recognize that the circuit court was in the best position to judge if their additional

designations were relevant to the issues on appeal or would have placed unnecessary expense

and burden on the Upchurches and this Court, respectively. Although the circuit court

determined that the costs of any additional appellate record designations should be assessed

to Dr. Lewis and Jackson Neurosurgery, the circuit court also allowed Dr. Lewis and Jackson

Neurosurgery to amend any additional designation as they wished. Upon review, we find

that the circuit court acted within its discretion. We therefore affirm the circuit court’s order

assessing the costs of any amended designations to Dr. Lewis and Jackson Neurosurgery.

CONCLUSION

27 ¶56. The Upchurches presented substantial testimony to support their claims that Dr. Lewis

breached the standard of care owed to Mary when he performed her surgery with only a

different manufacturer’s medical device available and that his negligence caused Mary’s

injuries. Because no properly admitted expert’s medical evidence contradicted the testimony

of the Upchurches’ expert medical witnesses, we conclude that there was insufficient

evidence to support the jury’s verdict in favor of Dr. Lewis and Jackson Neurosurgery. As

a result, with regard to the Upchurches’ appeal from the jury’s verdict and the circuit court’s

order denying their motion for JNOV in appellate case number 2023-CA-01296-COA, we

reverse and remand for a new trial consistent with this opinion. As to Dr. Lewis and Jackson

Neurosurgery’s consolidated appeal in appellate case number 2024-CA-00396-COA

challenging the circuit court’s order assessing to them the costs of any amended appellate

record designations, we find no abuse of discretion and affirm.

¶57. APPEAL NO. 2023-CA-01296-COA: REVERSED AND REMANDED. APPEAL NO. 2024-CA-00396-COA: AFFIRMED.

CARLTON, P.J., WESTBROOKS, McDONALD, LAWRENCE, McCARTY AND LASSITTER ST. PÉ, JJ., CONCUR. WILSON, P.J., DISSENTS WITH SEPARATE WRITTEN OPINION, JOINED BY BARNES, C.J. EMFINGER, J., NOT PARTICIPATING.

WILSON, P.J., DISSENTING:

¶58. The majority holds that because Dr. Lewis was not formally tendered or accepted as

an expert witness at trial, his testimony regarding the “standard of care was improper.”

However, the plaintiffs never objected to Dr. Lewis’s testimony on that ground or any other.

Therefore, any objection to Dr. Lewis’s testimony is waived. Evans v. City of Aberdeen, 926

28 So. 2d 181, 185 (¶13) (Miss. 2006).3 Indeed, the issue is doubly waived because the

plaintiffs do not even raise that issue on appeal. Rosenfelt v. Miss. Dev. Auth., 262 So. 3d

511, 519 (¶27) (Miss. 2018) (“[W]e decline to address an issue that has not been briefed on

appeal. . . . Simply put, we will not act as an advocate for one party to an appeal.” (quotation

marks omitted)). Because the issue was not raised at trial, there is no basis for the majority

to hold that the trial court erred or improperly admitted Dr. Lewis’s testimony.4 See Moffett

3 See also, e.g., Ellis v. State, 281 So. 3d 1092, 1101 (¶32) (Miss. Ct. App. 2019) (“Ellis asserts that the trial court erred by allowing Phyllis Crump, a forensic nurse practitioner, to testify as an expert witness because she was never offered or qualified as an expert. Crump was not offered or qualified as an expert, but Ellis did not object to any of Crump’s testimony on that ground. Therefore, this issue is also waived.” (citation omitted)); Branch v. State, 998 So. 2d 411, 414 (¶¶8-9) (Miss. 2008) (holding that although a witness “was never offered or qualified as an expert pursuant to Rule 702 of the Mississippi Rules of Evidence,” the defendant “waived the right to appeal this issue” because he “failed to object to [the witness’s] testimony pursuant to . . . Rule 702”); Cowart v. State, 910 So. 2d 726, 731 (¶22) (Miss. Ct. App. 2005) (“[The defendant] contends that Dr. Hayne was not formally tendered as an expert and that this failure to formally tender Dr. Hayne as an expert was reversible error. . . . Upon review of the record, we find that [the defendant] did not object to the failure to formally tender Dr. Hayne. . . . Therefore, [the defendant] has not preserved this argument for review, because he did not object to the failure to formally tender Dr. Hayne as an expert.”). 4 The trial court’s pretrial order listed Dr. Lewis as a “will call” fact and expert witness for the defendants. In addition, the defendants’ appellate brief and response in opposition to the plaintiffs’ motion to assess costs of the record on appeal (filed in the trial court) both state that they had designated Dr. Lewis as an expert in discovery. Although the defendants’ expert designations do not appear to be in the record on appeal, I would not fault the defendants for this omission. The defendants had no reason to cross-designate their expert designation for inclusion in the record on appeal because the plaintiffs did not raise that issue at trial or in their statement of issues on appeal. Moreover, “[i]t is an appellant’s duty to justify his arguments of error with a proper record or the trial court will be considered correct. The record on appeal must show such portions of the record of the trial court as are necessary for a consideration of the questions presented.” Pennington v. Dillard Supply Inc., 858 So. 2d 902, 903 (¶5) (Miss. Ct. App. 2003) (emphasis added) (citation omitted).

29 v. State, 49 So. 3d 1073, 1101 (¶91) (Miss. 2010) (“We will not hold a trial court in error on

appeal for a matter not presented to it for decision.” (quotation marks omitted)).

¶59. “Because [the plaintiffs] made no objection at the trial court level to the [defendants’]

failure to qualify [Dr. Lewis], [the plaintiffs] waived the issue,” and the majority “improperly

exclude[s] [Dr. Lewis’s] testimony from its decision concerning the [weight and sufficiency

of the evidence].” Evans, 926 So. 2d at 185 (¶13). As this Court has stated,

[i]f inadmissible testimony is received without objection, it becomes part of the evidence in the case and is usable as proof to the extent of its rational persuasive power. The fact that it was inadmissible does not prevent its use as proof so far as it has probative value. The inadmissible evidence, unobjected to, may be relied on in argument, and alone or in part it can support a verdict or finding. At the trial court level, a party may rely on the evidence to defeat a directed verdict motion; and on appeal, the party may use the evidence to uphold the legal sufficiency of the evidence to support a judgment.

Perkins v. State, 392 So. 3d 690, 696 (¶11) (Miss. Ct. App. 2024) (brackets omitted) (quoting

Shaheed v. State, 205 So. 3d 1105, 1110 (¶16) (Miss. Ct. App. 2016)).

¶60. At trial, Dr. Lewis testified that he was a board-certified neurosurgeon with thirty-

three years of experience and had performed the subject surgery numerous times. Dr. Lewis

further testified without objection that his treatment of Mrs. Upchurch and use of a Boston

Scientific pulse generator conformed to the standard of care. Because the plaintiffs never

objected to Dr. Lewis’s testimony, his testimony became part of the evidence in the case, and

it was sufficient to create a jury question on the issue and to sustain the jury’s verdict.

¶61. In addition, Dr. Lewis testified that the St. Jude lead that had been implanted in Mrs.

Upchurch seven years earlier was “bent and flimsy” and misshapen and could not be inserted

into any pulse generator or adapter. Dr. Narlin Beaty, testifying as an expert for the

30 plaintiffs, agreed that if “the lead was misshaped or damaged,” it was “no longer appropriate

to be implantable into any device.” Accordingly, the options at that point in the surgery were

to either end the surgery (leaving Mrs. Upchurch without a working spinal cord stimulator)

or implant a new lead. The original St. Jude lead had been implanted “percutaneously” with

a thin needle inserted into the epidural space around the spinal cord. However, it was not

possible to implant a new percutaneous lead because too much scar tissue would have

developed in the epidural space around the original lead for a new lead to be inserted in the

same space. Therefore, implanting a new lead required a laminectomy, a surgical procedure

that involves removing part of the lamina, which is the bony “roof of the spine.” A

laminectomy is a far more invasive procedure than a simple replacement of a pulse generator.

Dr. Lewis testified that he obtained consent from Mr. Upchurch and then proceeded with a

laminectomy to implant a new lead.

¶62. The plaintiffs’ theory of the case is that Dr. Lewis breached the standard of care by

attempting to use a Boston Scientific pulse generator with a St. Jude lead, which ultimately

required him to replace the St. Jude lead with a Boston Scientific lead, which required a

laminectomy, which caused Mrs. Upchurch’s hematoma and partial paralysis. However, Dr.

Lewis testified that due to its damaged condition, the St. Jude lead could not be inserted into

any pulse generator or adapter. As noted, plaintiffs’ expert Dr. Beaty agreed that a damaged

lead cannot be inserted into any manufacturer’s device. Accordingly, Dr. Lewis’s testimony

about the damaged condition of the original St. Jude lead provided an additional basis for the

jury to return a verdict in favor of the defendants.

31 ¶63. And although the majority finds “there was insufficient evidence to support the jury’s

verdict in favor of Dr. Lewis and Jackson Neurosurgery,” it is important to remember that

the defendants did not bear any burden of proof at trial. The plaintiff in a medical

malpractice case bears the burden of proving each essential element of her claim. Johnson

v. Pace, 122 So. 3d 66, 68 (¶8) (Miss. 2013). As the Mississippi Supreme Court has

explained, “[a] plaintiff has the burden of proof, and must offer evidence that persuades the

jury. The jury is not required to believe or trust the evidence submitted by the plaintiff, and

is free to accept all, part, or none of the plaintiff’s evidence. A defendant is not required to

prove or rebut anything.” Thompson v. Dung Thi Hoang Nguyen, 86 So. 3d 232, 236-37

(¶13) (Miss. 2012) (emphasis added). The jury could have returned a defense verdict simply

because it found that the plaintiffs’ experts were not persuasive or credible. Therefore, the

verdict and judgment should be affirmed.

¶64. Because Dr. Lewis’s unobjected-to testimony provided a sufficient basis for

reasonable jurors to find that the plaintiffs did not prove the essential elements of their

claims, I respectfully disagree that the plaintiffs are entitled to any sort of partial judgment

notwithstanding the verdict or a new trial. See generally White v. Stewman, 932 So. 2d 27,

32 (¶10) (Miss. 2006) (standard of review for denial of JNOV); Bobby Kitchens Inc. v. Miss.

Ins. Guar. Ass’n, 560 So. 2d 129, 131-32 (Miss. 1989) (standard of review for denial of a

new trial). The conflicts in the testimony were appropriately submitted to and resolved by

the jury at trial and should not be reweighed by this Court on appeal. Accordingly, I

32 respectfully dissent.5

BARNES, C.J., JOINS THIS OPINION.

5 Because the majority reverses the judgment in the plaintiffs’ appeal (No. 2023-CA- 01296-COA), the defendants’ appeal regarding the cost of the record on appeal (No. 2024- CA-00396-COA) is moot. Because the judgment is reversed, all costs of the appeal will be taxed against the defendants anyway. See M.R.A.P. 36(a), (c). Therefore, there is no need to address the issue if the judgment is reversed.