The Issue The issue in this case is whether Ailani Sanchez suffered a birth-related injury as defined by section 766.302(2), Florida Statutes, for which compensation should be awarded under the Florida Birth-Related Neurological Injury Compensation Plan (the Plan).
Findings Of Fact Ailani Sanchez was born a live infant at 5:46 a.m., on October 29, 2015, at Lakeland Regional Medical Center. Ailani was a single gestation, weighing 2,950 grams at birth. Ailani was delivered via cesarean section for suspected abruption/velamentous insertion of cord by Dr. Zollicoffer who was a NICA participating physician on October 29, 2015. Ailani's Apgar scores were 2/4/4. Upon delivery, she was floppy and pale and had no respiratory effort. Pulse oximetry was within target saturations for age and her heart rate remained 100 or greater. She was intubated at seven minutes of age and transferred to the Neonatal Intensive Care Unit (NICU). No seizures were noted. Ailani had increasing spontaneous respiratory effort and whole body cooling was started prior to her transfer to St. Joseph's Hospital NICU on October 29, 2015. Upon admission to St. Joseph's Hospital on October 29, 2015, Ailani was lethargic with decreased reactions to stimuli, but appeared pink and well perfused. Neurologically, she was noted to be improving; she was breathing spontaneously and moving all extremities to stimuli. After a complicated newborn hospital course, Ailani was ultimately discharged from St. Joseph's Hospital on January 6, 2016. At the time of her discharge, she was noted to be feeding by mouth and was overall gaining weight. Prior to her discharge, an EEG on October 30, 2015, showed seizures predominantly on the right side of her brain and generalized brain dysfunction. A brain MRI obtained on November 5, 2015, revealed restricted diffusion related to acute infarction in the right temporal occipital region with laminar necrosis. Additional laminar necrosis in the frontal lobes and insular cortex bilaterally was noted. An EEG on November 16, 2015, was consistent with nonspecific cerebral dysfunction with occasional sharp waves in the temporal parietal regions bilaterally with no evidence of seizures and irregular slow waves with slightly more predominance to the right. Ailani was seen for a newborn visit by her pediatrician, Dr. Bou Salvador, on January 7, 2016. Nutritionally, she was noted to be breast feeding adequately, with supplements with formula. Developmentally, she was noted to have equal movements of all extremities and follow midline. She responded to a bell and was able to lift her head while lying on her stomach. Examination of her spine, extremities, and peripheral pulses were all normal. Neurologically, she was reportedly normal, with normal strength, tone, and reflexes reported. On January 19, 2016, Ailani was evaluated at All Children's Outpatient Care upon referral by St. Joseph's Hospital secondary to hypoxic ischemia. The occupational therapist's impression included decreased bilateral coordination, decreased developmental milestones, decreased gross motor skills, decreased play skills, decreased strength, and fine motor deficits. Skilled therapy was identified to have the potential to improve her functional level in the areas of manipulation. It was recommended that Ailani undergo 30 minutes of occupational therapy once a week for six months. Her prognosis for achieving goals established by her therapist was noted to be excellent. On February 4, 2016, Ailani was evaluated for participation in, and deemed eligible for, the Early Steps Program. On February 18, 2016, Ailani was evaluated by Dr. Qureshi at Kids Neurology. Developmentally, she was noted to smile and coo and focus. It was noted that Ailani had three seizures at the age of one day old, but none since. At this time, she was taking Keppra and Phenobarbital, from which she was being weaned. A sleep deprived EEG, obtained since the last visit, was normal. She was noted to be doing very well neurologically. Her physical examination revealed she was lifting her chest and head with her arms extended. Early head control with bobbing motion was noted. She was noted to say "aah," smile, and follow pass midline. The plan noted at this time was to continue to wean and discontinue Keppra and Phenobarbital. Ailani was again seen by Dr. Bou Salvador on March 4, 2016, for her four-month well visit. Nutritionally, she was noted to be feeding with formula adequately. She had been started on solids for one to two feeds. Developmentally, she was noted to squeal and laugh. She was able to follow 180 degrees. She turned to void and was able to hold her head up 90 degrees while lying on her stomach. She was able to sit with support with her head up. She was able to pull to sit with no head lag. She could bring her hands together and had no persistent fist clenching. Her physical examination was normal. Her neurological examination was also normal, with normal strength, tone, and reflexes reported. Ailani was again seen by Dr. Bou Salvador on May 4, 2016, for her six-month well visit. Nutritionally, she was noted to be breast feeding adequately. Developmentally, she was noted to be social and smiling responsively. Adaptive equal movements of all extremities and the ability to follow midline were noted. She could respond to a bell and was able to lift her head while lying on her stomach. A physical examination was normal. A neurological examination was also normal, with normal strength, tone, and reflexes reported. On May 24, 2016, Ailani returned to Dr. Qureshi at Kids Neurology. It was noted that Ailani had been weaned from her seizure medication and had had no seizures for the last three months. She was noted to be doing very well neurologically. Physically and developmentally, she was noted to have no head lag, to be rolling over, to have her chest up in a prone position, to be trying to crawl, to be lifting her head, and to be sitting briefly unsupported. She was also noted to be leaning forward on her hands, engaging in bounce activity, supporting most of her weight, reaching out and grasping large objects, transferring from hand to hand, babbling, enjoying mirror, and using polysyllable sounds. She was noted to be feeding herself. Dr. Qureshi reported that Ailani was in occupation therapy but that it was on hold since her evaluation was "pretty unremarkable." Ailani was noted to be progressing well for her age and was receiving Early Steps intervention once a week at home. She was given a prescription of Phenobarbital for use only if a seizure occurred. On June 18, 2016, Ailani was seen by Dr. Frances Arrillaga at Pediatric Cardiology Associates for a cardiology consultation secondary to a history of pulmonary hypertension, and an echocardiogram that showed a patent foramen ovale (PFO). Ailani's mother reported that since her discharge from St. Joseph's, she was doing well. Cyanosis, difficulty breathing and unexplained diaphoresis and feeding problems, were denied. An echocardiogram on this date showed a PFO, with otherwise normal anatomy. There were normal right ventricular (RV) pressures, normal left ventricular (LV) size and function. No cardiovascular restrictions were given and she was told to return in one year for further follow up. Ailani was again seen by Dr. Bou Salvador on August 4, 2016, for her nine-month well visit. Nutritionally, she was reported to be feeding adequately. She was feeding 2 to 3 varieties of solid foods with no problems and was starting with a cup for water and juice. Developmentally, she was reported to be playing pat-a-cake and looking for fallen objects. She could bang two cubes in her hand with thumb-finger grasp. She could say "dada" and "mama" and walk while holding on. She was also noted to be crawling and standing momentarily. Her physical and neurological examinations were noted to be normal, with normal strength, tone, and reflexes noted. An August 22, 2016, a progress note from Early Intervention reflects that Ailani was babbling two syllables together, was happy, pulling to a stand and cruising along furniture, and was responding to her name. Attendance at Early Intervention was noted to be consistent and once a week. Ailani was again seen by Dr. Bou Salvador on November 3, 2016, for her 12-month well visit. Nutritionally, she was noted to be eating two to three varieties of solid foods with no problems and was feeding herself finger foods. Developmentally, she was reported to be playing pat-a-cake and drinking from a cup. She was able to bang two cubes held in her hands with thumb-finger grasp. She was saying "mama" and "dada," imitated speech sounds, could say three words other than "mama" and "dada," and understood "no." She was able to walk while holding on, and was reported to stand alone and walk well. A physical examination revealed normal extremities. A neurologic examination was also normal, with normal strength, tone, and reflexes reported. On November 21, 2016, Ailani returned to Dr. Qureshi at Kids Neurology. It was noted that Ailani had been weaned off medications six months earlier and had no seizure activity since. She was noted to be doing very well. It was noted that no therapy was being provided at this time, although she was evaluated for occupational therapy but did not qualify for it. Developmentally, she was noted to be walking with one hand held, rising independently, taking several steps, getting to sitting, pulling to stand, standing for two seconds, saying a few words besides "mama" and "dada," playing ball game, making postural adjustment to dressing, waiving "bye bye," and indicating what she wants. She was noted to have pincer grasp, releasing objects to others when grabbed, and banging two things. Dr. Qureshi noted "she is doing amazing right now." A December 24, 2016, emergency room record (for a cough/choking episode after eating a piece of Dorito) from Florida Hospital Tampa reflects that Ailani had not had seizures since birth, and had been off Keppra and Phenobarbital for almost a year. A physical examination revealed an active, well- developed, and well-nourished child. Neurologically, she was noted to be awake, alert, and interacting with family and staff. She was also noted to be active and playful. An Early Intervention progress note from February 15, 2017, reflects Ailani had age-level play skills, could communicate using vocalizations and some single words, could follow routine directions, and was independent with walking and floor transfers. Good progress was noted to be made, many goals were reported met, and the parents decided to reduce services to one time per month. On January 30, 2017, Ailani was reevaluated for participation in Early Steps. It was noted that Ailani's mother had no concerns at this time. The report notes that Ailani liked the slide, liked to kick the ball, liked to play with her siblings and cousins, and that she is very curious. No hearing or vision concerns were noted. It was reported that many of her goals had been met, and that Ailani was using a variety of vowels and consonants, identifying at least three family members when named, that she was saying a variety of words, and was using a sign for "more food." Ailani was noted to still be eligible for Early Steps secondary to her diagnosis of hypoxic ischemic encephalopathy. Ailani was seen by Dr. Bou Salvador on March 28, 2017, for her 16-month well visit. She was noted to have good eating habits and a good appetite. No mealtime problems were reported, and she was noted to be eating solid foods with no problems. She was noted to have socially appropriate behavior for her age. She was talking well and was able to balance on one foot for five seconds, could throw a ball overhead, and pedal a tricycle. Her orthopedic and neurologic examinations were normal, with normal strength, tone, and reflexes reported. At the request of NICA, Donald C. Willis, M.D., who specializes in obstetrics and gynecology and maternal-fetal medicine, reviewed the medical records included in the Stipulated Record as Joint Exhibits A through G. In his report dated August 2, 2017, which was admitted into evidence without objection, Dr. Willis noted in pertinent part that Ailani's mother was cramping when she presented to the hospital, and was three centimeters dilated with suspected amniotic membranes ruptured. Contractions were noted to be occurring occasionally. Medical records indicated the presence of late decelerations on admission, which progressed to bradycardia, for which an immediate Cesarean section was recommended. Dr. Willis observed that Ailani was depressed at birth with Apgar scores of 2/4/4, and that cord blood gas was abnormal with a pH of only 6.97. He further noted that Ailani was floppy, pale, and had poor perfusion; that bag and mask ventilation was initiated, followed by intubation for continued respiratory distress; that hypotension was present and required IV fluids; that the initial blood count was low; and that Ailani remained acidotic after birth with a pH of 6.7 and a base excess of -27 at 90 minutes after birth. Dr. Willis further noted Ailani's hospital course consistent with her medical records and ultimately opined that “there was an obstetrical event that resulted in loss of oxygen to the baby's brain during labor, delivery and continuing into the immediate post delivery period. The oxygen deprivation resulted in brain injury.” Dr. Willis was unable to comment about the severity of the injury, however. At the request of NICA, Laufey Y. Sigurdardottir, M.D., who is board certified in neurology and specializing in pediatric neurology, reviewed the medical records included in the Stipulated Record as Joint Exhibits A through G, and performed a thorough examination of Ailani on October 18, 2017. Dr. Sigurdardottir's summary of Ailani's medical history, along with her findings upon a full physical and neurological examination, is documented within her written report, which was admitted into evidence without objection. Dr. Sigurdardottir noted that Ailani was a non-dysmorphic, interactive toddler with normal facial features and apparently intact vision. No abnormalities in Ailani's extremities were noted other than occasional toe walking. Neurologically, Ailani was noted to be interactive, curious, and exhibiting normal joint attention. Ailani exhibited pretend play with a stethoscope, said the word "mom" a few times, pointed to her mouth when asked to do so, enjoyed playing with a tablet computer, shook her head for "no," exhibited understandable words, and exhibited no autistic features. Cranial nerves were intact, facial grimacing was symmetric and normal, and hearing seemed intact. No drooling was noted. Muscle tone was noted to be normal, strength was full and symmetric and deep tendon reflexes were symmetric and within normal limits. Gross and fine motor skills were noted to be within normal limits for age. Overall, Dr. Sigurdardottir determined that despite her initial abnormal neurological examination, and delays in early development, Ailani's current neurologic and developmental functioning is age-appropriate. She went on to opine in relevant part that, Ailani is not found to have substantial delays in motor and mental abilities at this time . . . . In review of available documents, there is evidence of impairment consistent with a neurologic injury to the brain or spinal cord acquired due to oxygen deprivation . . . . The prognosis for full motor and mental recovery is excellent and the life expectancy is full In light of evidence presented I believe Ailani does not fulfill criteria of a substantial mental and physical impairment at this time. I do not feel that Ailani should be included in the NICA program. Neither Petitioner nor Intervenor submitted or introduced into evidence any expert reports rebutting the opinions of Dr. Willis and/or Dr. Sigurdardottir.
The Issue At issue is weather Tyler Anthony Carter, a minor, qualifies for coverage under the Florida Birth-Related Neurological Injury Compensation Plan (Plan).
Findings Of Fact Stipulated facts Victoria Knight Carter and Roy Carter are the natural parents of Tyler Anthony Carter, a minor. Tyler was born a live infant on February 7, 2005, at North Shore Medical Center, a licensed hospital located in Miami, Florida, and his birth weight exceeded 2,500 grams. Obstetrical services were delivered at Tyler's birth by Ramon Hechavarria, M.D., who, at all times material hereto, was a "participating physician" in the Florida Birth-Related Neurological Injury Compensation Plan, as defined by Section 766.302(7), Florida Statutes. Coverage under the Plan Pertinent to this case, coverage is afforded by the Plan for infants who suffer a "birth-related neurological injury," defined as an "injury to the brain or spinal cord . . . caused by oxygen deprivation or mechanical injury occurring in the course of labor, delivery, or resuscitation in the immediate postdelivery period in a hospital, which renders the infant permanently and substantially mentally and physically impaired." § 766.302(2), Fla. Stat. Here, the proof demonstrated that Tyler's delivery was complicated by a shoulder dystocia, which caused a brachial plexus injury, that resulted in a weakness (an Erb's palsy) in the left upper extremity. Otherwise, Tyler was not shown to suffer any injury at birth. To address the nature and significance of Tyler's injury, NICA offered the testimony of Michael Duchowny, M.D., a physician board-certified in pediatrics, neurology with special competence in child neurology, and clinical neurophysiology.1 (Respondent's Exhibit 1, deposition of Dr. Duchowny). Dr. Duchowny evaluated Tyler on October 17, 2007, and reported the results of his physical and neurological evaluation, as follows: PHYSICAL EXAMINATION reveals an alert, cooperative 2 1/2-year-old, well-developed and well-nourished toddler. Tyler[] weighs 29 pounds. His skin is warm and moist. There are no dysmorphic features or neurocutaneous stigmata. Head circumference measures 49.2 centimeters, which is within standard percentiles for age. The fontanels are closed. There are no cranial or facial anomalies or asymmetries. The neck is supple without masses, thyromegaly or adenopathy. The cardiovascular, respiratory, and abdominal examinations are unremarkable. Tyler's NEUROLOGICAL EXAMINATION reveals an alert and sociable toddler. His speech is fluent and appropriately articulated. He maintains an age appropriate stream of attention. His social skills are appropriately developed for age. Cranial nerve examination is unremarkable. The extraocular movements are fully conjugate in all planes and the pupils are 3 mm and briskly reactive to direct and consensually presented light. A brief funduscopic examination is unremarkable. There are no significant facial asymmetries. The uvula is midline and the pharyngeal folds are symmetric. The tongue is moist and papillated. Motor examination reveals an asymmetry of the upper extremities. There is slightly diminished muscle bulk in the distal left upper extremity. Tyler is unable to raise the left arm past neutrality. He tends to posture the left arm with flexion at the elbow and wrist. Tyler cannot fully supinate the left hand. He can build a tower with using either hand and has bimanual dexterity. However, he demonstrates a consistent right hand preference. There are no fixed contractures. The deep tendon reflexes are 2+ in the lower extremities and the right upper extremity but 1+ at the [left] biceps. The sensory examination is intact to withdrawal of all extremities to stimulation. The neurovascular examination reveals no cervical, cranial or ocular bruits and no temperature or pulse asymmetries. In SUMMARY, Tyler's neurological examination reveals a mild left Erb's palsy, which was likely acquired during delivery due to traction on the brachial plexus. In contrast, there are no abnormalities referable to the right upper extremity or the lower extremities. Tyler's mental functioning is appropriate for age level. (Joint Exhibit 1, Report of Dr. Duchowny, dated October 17, 2007; Respondent's Exhibit 1, pp. 15 and 16). An Erb's palsy, as evidenced by Tyler, is a weakness of an upper extremity due to damage to the nerve roots of the left brachial plexus, a peripheral nerve injury, and does not represent an injury to the brain or spinal cord (the central nervous system). (Respondent's Exhibit 1, pp. 10 and 11).2 Moreover, the physical impairment Tyler suffers is mild, as opposed to substantial, and there is no compelling evidence of mental impairment, much less substantial mental impairment. (Respondent's Exhibit 1, pp. 8-10). Ackley v. General Parcel Service, 646 So. 2d 242, 245 (Fla. 1st DCA 1994)("The determination of the cause of a non-observable medical condition, such as a psychiatric illness, is essentially a medical question."); Thomas v. Salvation Army, 562 So. 2d 746, 749 (Fla. 1st DCA 1990)("In evaluating medical evidence, a judge of compensation claims may not reject uncontroverted medical testimony without a reasonable explanation."). Consequently, while Tyler may have suffered a mechanical injury, permanent in nature (to his left brachial plexus) during the course of birth, he does not qualify for coverage under the Plan.
The Issue The issue in this case is whether Samuel Joseph Hereford suffered an injury for which compensation should be awarded under the Florida Birth-Related Neurological Injury Compensation Plan (Plan).
Findings Of Fact Steven and Theresa Hereford are the natural parents of Samuel Joseph Hereford. Samuel was born on May 31, 2009, at Memorial Hospital, which is a licensed hospital located in Jacksonville, Florida. Samuel weighed in excess of 2,500 grams at birth. Obstetrical services at Samuel’s birth were provided by a physician participating in the NICA program. Samuel has permanent and substantial mental and physical impairments. Samuel is Mrs. Hereford’s fourth biological child. She chose to use the services of a midwife for Samuel’s birth, but to deliver at the hospital. Mrs. Hereford presented to Memorial Hospital at approximately 4:00 a.m., on May 31, 2009. When she was first examined, it was determined that she was dilated at 8 centimeters. Mrs. Hereford recalls that the nurse midwife asked her if she was “ready to get this over with.” When Mrs. Hereford replied “yes,” the nurse midwife ruptured Mrs. Hereford’s membranes. She immediately began experiencing intense pain, “a pain like I had never experienced before.” Samuel’s head was delivered and she continued to push while in extreme pain. At some point, she was turned over and Samuel was delivered. Samuel was born by vaginal delivery at 5:17 a.m. His delivery was complicated due to a shoulder dystocia that resulted in a six-minute delay between his head and the rest of his body being delivered. He did not cry when he was first delivered. Mrs. Hereford recalls seeing all of the medical personnel around Samuel’s bed and recalls maybe hearing a faint cry at some point. After an undetermined amount of time, Samuel was brought to her very briefly. She recalls that he was swaddled and that his face was blue. He was not crying or making noise. Mr. Hereford was present for Samuel’s delivery. He recalls that when Samuel was delivered, he looked lifeless. He was blue and did not make any noise. Samuel was taken to a table where the medical personnel began resuscitation. He recalls them performing chest compressions and putting an oxygen mask on him. Samuel looked swollen, blue, puffy and “like he had just been beat up.” He also recalls that Samuel was swaddled, taken to Mrs. Hereford briefly, then taken to the NICU. Samuel’s one-minute Apgar score was 3, his skin was pale and blue, his muscle tone was absent, and his heart rate was below He received “face mask ventilation x 2 minutes, blow by oxygen and cardiac compression. Began gasping less than 1 minute of age. HR over 100 by 90 seconds of age.” His five-minute Apgar was 8. At about six hours of life, Samuel was transported to Wolfson’s Children’s Hospital for further evaluation. Mr. Hereford described how Samuel looked when he first saw him at Wolfson’s: “Well, he still looked like he had been through trauma. He was still blue. He was still puffy. He was still bruised. I remember seeing a cut on his shoulder. That’s what I remember how he looked.” He stayed in the NICU at Wolfson’s for four days. After leaving Wolfson’s, the Herefords took him straight to the pediatrician’s office, which then referred them to Dr. Joyce, a board-certified pediatric cardiologist. Dr. James Joyce first examined Samuel on June 5, 2009. His notes from that first visit reflect history obtained from Samuel’s parents and from his examination of Samuel: CC Abnormal echocardiogram and cardiomegaly on chest X-ray HPI Discharged yesterday from Wolfson Children’s Hospital NICU after 4 day stay. Admitted in transfer from Memorial Hospital for cardiomegaly on initial chest X-ray performed for evaluation of oxygen requirement. Spontaneous vaginal delivery at -37 weeks gestation at Memorial Hospital complicated by shoulder dystocia, then initially low Apgars requiring resuscitation for the first few minutes of life. He stabilized on nasal prong oxygen and IV fluids with glucose. After transfer to WCH he required nasal oxygen and IV fluids for two days. He also had hypoglycemia on the first two days with low of 31 mg/dl at 5:30AM on 06/03/09. His pCO2 ranged from 45 to 53mmHg from 05/31/09 to 06/02/09. His hematocrit rose from 58.6 on 05/31/09 to high of 71.5 on 06/02/09, then fell to 59% on 06/02/09 before rising to 65.7% yesterday morning before discharge. Initial echocardiogram to evaluate CXR finding of cardiomegaly on 05/31/09 showed bidirectional flow across a “moderate-size” patent ductus arteriosus and mildly depressed LV systolic function with EF of 52% and FS of 25%. His second and last echocardiogram on 06/03/09 showed left to right shunting across the PFO, no residual PDA shunting, mild tricuspid regurgitation, mild residual pulmonary hypertension with estimated PASP -45mmHg, and decreased RV and LV systolic function with estimated EF -40% However, a Cardiology consult was not ordered. He was advanced to room air and p.o. feedings on the third day of life and jaundice developed with a peak total bilirubin of 20.8 on 06/03/09. His bilirubin decreased to 14 on the day of discharge 06/04/09, but increased to 15mg/dl last night after they had been having problems with his bililight bed at home. Today he was brought in by his parents without other complaint. He is breast feeding every 2 hours for about 30 minutes each time. Denied history of feeding difficulty, breathing difficulty, syncope, or sweats with feeds. ROS Mildly sleepy most of the time. Not as alert as previous babies. Bruising of shoulders from difficult delivery. Normal renal ultrasound yesterday. Entire review of systems was negative, except as above. PMH Gestation complicated by polyhydramnios, thick heart walls on OB ultrasound, and then preterm labor after 33 weeks gestation. Spontaneous vaginal delivery at -37 weeks gestation at Memorial Hospital complicated by shoulder dystocia. s/p early transient neonatal hypoglycemia. s/p early neonatal polycythemia. Neonatal jaundice Decreased RV and LV systolic function since first day of life. SH He lives with parents, sisters 16 and 18y/o, brothers 19y/o and 15 months. FH Parents alive and well. No family history of congenital heart disease, sudden cardiac death, pacemaker, or early (<age 40 yr.) myocardial infarction or stroke, grandparents have hypertension and high cholesterol with history of stroke and heart attacks. Allergies NKDA Meds No meds, but on home phototherapy for jaundice. Vitals Wt: 8.8 lb Ht: 21.5 in BP: 86/52 P: 127 RR:28 BMI: 13.2 PE Oxygen saturation in room air 98%. Awake and in no distress. Well developed, well nourished appearing. Mildly lethargic. Normocephalic, except for slight molding and mild bilateral ecchymosis of lower eyelids. Mild scleral icterus. No ear, nose or throat inflammation. Mucosae pink and moist. Neck supple without lymphadenopathy, goiter, or jugular venous distention. Chest symmetrical without deformity. Lungs clear to auscultation. Heart with regular rhythm and normal rate. Normal first and second heart sounds. No click, gallop, murmur or rub heard. No lift or thrill felt. Abdomen nondistended, nontender, with normal bowel sounds and no evidence of hepatomegaly, splenomegaly or mass. No abdominal bruit heard. Polydactyly with 6th finger on right hand. No extremity edema. No joint swelling or tenderness. Pulses 2+ and equal in all four extremities. Normal skin temperature and furgor. Plethoric skin color with superimposed jaundice. No rash seen. No weakness, incoordination, or tremor. Grossly normal muscle tone. ECG: normal sinus rhythm, diffuse T wave inversion in inferior and anteroseptal leads and mildly prolonged QTc interval suggestive of ischemic myocardial injury. Echocardiogram: very mild Ebstein anomaly of the tricuspid valve with mild regurgitation, moderately dilated RV, severe RVH, other cardiac chambers of normal size, moderately decreased biventricular systolic function, LV EF -40%, trivial mitral valve regurgitation, no pericardial effusion, no residual PDA, no aortic coarctation. no AS, normal coronary artery origins. A/P #CHRONIC SYSTOLIC HEART FAILURE (428.22): EF -40%, mildly to moderately decreased left, probable cardiomyopathy, R/O ischemic CMP vs. noncompaction or other congenital CMP #EBSTEIN’S ANOMALY (746.2): Mild tricuspid regurgitation. # secondary Pulm Hin /OT Ch P Heart Disease (416.8): resolving primary pulmonary hypertension of the newborn. # POLYCYTHEMIA NEONATORUM (776.4): still plethoric appearing. # UNSPECIFIED FETAL AND NEONATAL JAUNDICE (774.6): still jaundiced appearing. # SPONTANEOUS ECCHYMOSES (782.7): ecchymosis of both lower eyelids, R/O IVH or basilar skull fracture. # POLYDACTYLY OF FINGERS (755.01): 6 fingers on right hand. I called and discussed case with Dr. Caron- Canas, her Pediatrician on-call. Working diagnoses and prognosis explained to parents. Therapeutic plan outlined. ADVISED/ORDERED: Admit Orders: Admit to Wolfson children’s hospital on telemetry to the service of Dr. James J. Joyce Diagnosis: chronic systolic heart failure, R/O cardiomyopathy, neonatal jaundice vital signs every 4 hours with BP accurate I & O, daily weights breast feedings per mother’s schedule Labwork now: CBC, complete metabolic profile, troponin, CK-MB PA and lateral Chest X-ray today (regarding CHF) Digoxin 16micrograms (0.32ml of 50mcg/ml oral solution p.o. now and every 12 hours thereafter Captopril 0.7 ml of 1 mg/ml oral solution) p.o. now and every 8 hours thereafter 12-lead ECG in the morning tomorrow please call Dr. J. Joyce when patient arrives on the ward (296-7771). In his deposition taken August 5, 2016, Dr. Joyce described Samuel when he first examined him, as having bruising of his lower eyelids, was plethoric (darkish pink) and had mild jaundice. Dr. Joyce performed an electrocardiogram (ECG) and an echocardiogram at his initial evaluation on June 5, 2009, and was asked about the findings from these tests: Q: Was that something that you performed? A: Here in the office, yes. Q: And what did you find as a result of that ECG? A: He had abnormal T-wave inversions inferiorly and from the anteroseptal leads and mildly prolonged QT intervals suggestive of ischemic injury. * * * Q: You said suggestive of ischemic myocardial injury. What does that mean in layman’s terms? A: Like an infarction. Well, like a heart attack or an injury to the muscle that is from low blood flow. That’s what ischemia is. Low blood flow to the muscle causing damage. Q: Then an echocardiogram was also performed; is that right? A: That’s correct. Q: And you found that he had a very mild Ebstein’s anomaly? A: Yes. That’s a deformity of the tricuspid valve, but it’s extremely mild. Very mild. Q: Very mild. Okay. And as a result of this workup you decided to admit him to Wolfson’s Children’s Hospital; is that right? A: Correct. Q: And at Wolfson’s what was your role in Sam Hereford’s care? Did you serve as his attending physician? A: As I recall, yes. I got a neurology consult and -- well, neurology in particular. I was very concerned about that because he was floppy or hypotonic. He had bruising on his head. And the history that I saw, the history from the time of delivery and thereafter. It was obvious in the record that he had a period of asphyxia. * * * And he [had] low sats, low oxygen saturation and thereafter had to be put on oxygen. Also blood pressure was low so they gave him a bolus of fluid. And that brought the blood pressure up. So this was a kid who was in distress at birth, quite clearly. * * * The bloodwork back when he was admitted the first time to Wolfson’s, he had -- at Memorial Hospital he had prolonged and extensive hypoglycemia. Low blood sugar. Q: What does that indicate to you? A: Well, it certainly can be increased insulin from maternal gestational diabetes, but there was no history of that here. Although with his weight being as heavy, as big as he was, that’s certainly a possibility. But when you have hypoxia or asphyxia you go into anaerobic metabolism and you use glucose up a lot quicker than you do with aerobic metabolism. So his asphyxia alone could cause hypoglycemia. He had very extensive and prolonged hypoglycemia. He also had thrombocytopenic where his platelet count was low. Then during the first couple of days in the hospital his creatinine elevated, which implies that he had injury to his kidneys. Acute tubular necrosis can be caused by asphyxia. Also he was polycythemic. His hematocrit actually went up to 71 percent, quite high. And that can also be due to asphyxia. Asphyxia’s a risk factor for polycythemia and elevated creatinine, hypoglycemia, and thrombocytopenia. So all of those are circumstantial pieces of evidence, along with the history of him being stuck for six minutes during a very difficult delivery, so that all led to that. And we did admit him. And, now, on my admission, what I did do, because I was suspicious because of the EKG and the history that he had, the hypoxic ischemic injury to his entire body, I figured it obviously would include that heart. So I checked for serum troponin and CPK or CK- MB, creatinine kinase myocardial band, or MB. And those were all positive. Those two were positive, showing that he did have injury and necrosis of his myocardium. These were specific for the myocardium. So those enzymes showed that he had myocardial necrosis. Q: So the troponins -- am I saying that right? A: Yes. Troponin I is the particular one he had. Q: So the troponin I showed that he had a myocardial injury, an injury to his heart. A: Yeah. An infarction. Actually death of the cells. It gets released into the blood. Q: And myocardial infarction is death of heart tissue; correct? A: Right. From low blood flow. From inadequate nutrition, blood flow, or oxygenation, or both. Q: And the troponin levels that you noted, were they high? A: They were high. Because, again, he was five days old at that time, five or six days old. Q: Six days old, I believe. A: Yes. He was old enough that it was on its way down. It went down. On recheck a couple of days later it was dropping. Q: Does -- A: For it to still be high six days after birth meant that it was pretty darn high earlier. Because it bumps up and then it comes down over time. * * * All this being consistent with a watershed or diffuse myocardial infarction, which would go along with the history of the birth injury, and the low Apgar, the resuscitation, et cetera. Again, I’m inferring asphyxia from all the evidence. * * * Q: So, if I understand you, and tell me if I don’t, from what you are saying, all of his records that you were able to see from his birth and also the evaluation of him and the following of him in the hospital led you to believe that he suffered a hypoxic ischemic event during birth; is that right? A: Yes. * * * Q: So after you admitted him to the hospital, and I believe in your note you were indicating that you were attempting to at least rule out an ischemic CMP versus non-compaction or other congenital CMP. What does that mean? A: Cardiomyopathy. He does have evidence of non-compaction cardiomyopathy. Q: What is that? A: It’s an abnormality of the heart muscle. The form of the heart muscle is more trabeculated. It’s not as compact. That’s where the word non-compaction comes in. But there’s many different forms—different degrees of non-compaction. Mild, moderate, severe. There’s also many different known genetic origins for that and many that we don’t have genetic origins for. We don’t know. Dr. Joyce explained that cardiomyopathy can make someone more sensitive to a hypoxic ischemic event, but it was not the reason for the event. “In other words, it can make things worse than they would be otherwise, but it’s not the main reason that you’re going to have that malfunction.” When asked whether non- compaction syndrome, as a prenatally acquired congenital disorder, can cause a child to have a myocardial infarction post-delivery, he replied, “Not in and of itself, no.” He continued: Q Had that hypoxic ischemic event not occurred, let’s say, in your opinion, could Samuel still have the heart problems he had as a result of the prenatally acquired congenital heart abnormalities we know he had? A He wouldn’t have had the extent of dysfunction and he wouldn’t have had positive troponin and CK-MB. Q Based on the non-compaction cardiomyopathy alone? A Correct. Q What other factors, other than a hypoxic ischemic could contribute to the non- compaction cardiomyopathy that would lead a child to have heart conditions like Samuel had post-delivery. * * * A You’re asking what else can do this. There isn’t a whole lot more in a newborn baby. You have to really use your imagination to come up with why you’re going to have a diffuse subendocardial myocardial infarction in a newborn baby, other than hypoxic ischemic encephalopathy and some other wild things. Prolonged shock. High dose epinephrine. Those kind of things. You have to come up with that. Dr. Joyce was also asked about Ebstein’s anomaly: Q . . . Were you able to determine whether or not that Ebstein’s anomaly caused the myocardial infarction? A No, it did not. Q How do you know that? A Ebstein’s anomaly, what it is, is an abnormality of the tricuspid valve. A valve is a door. It’s just a simple door, a doorway. The tricuspid valve has three doors to the doorway. He had a slight abnormality to the door. The door wasn’t quite normal. But it was a very mild abnormality. His regurgitation at birth was listed as mild. No, I’m sorry, moderate. It was moderate at birth and then it quickly became mild by day four. The second echocardiogram was mild. That was associated -- when it was moderate, and even mild, it was associated with pulmonary hypertension that was severe and moderate. So at birth he had severe pulmonary hypertension and moderate tricuspid valve regurgitation. By day five or so, the second echocardiogram in his initial hospitalization, the pulmonary hypertension was down to moderate and his tricuspid valve regurgitation was down to mild. And the reason is because the pulmonary hypertension, that high pressure, is back against that right sided pumping chamber, the one that has the tricuspid valve. We commonly see it in kids with normal tricuspid valves that have pulmonary hypertension, we will see more severe tricuspid valve regurgitation. So the tricuspid regurgitation wasn’t significantly out of proportion to the pulmonary hypertension. And it certainly was not enough to cause heart failure. Q Right. I have a copy here of -- A And just as an aside, you will notice that, if you look at the record, the echocardiograms that were reported in the hospital, they didn’t mention non-compaction, they didn’t mention Ebstein’s anomaly on their echo reports. The reason was because both of them were relatively mild. Again, I did an extra year of training in echocardiography. I used to run the echocardio- -- the echo lab at Wolfson Children’s Hospital. I’m a fellow of the American Society of Echocardiography. I see more detail in echocardiograms than most cardiologists because of that background. Q So -- A Again, these were mild, mild abnormalities. And unfortunately, you go, oh, there’s Ebstein’s anomaly, that must be the reason for heart failure. Well, Ebstein’s can be very, very mild or very severe. And it can have all sorts of forms and problems with function. But, again, this was a very mild one. And the non-compaction is relatively mild. Because it also was missed. Q Okay. So what you’re saying is there were echocardiograms that were taken before you were involved but they missed the Ebstein’s anomaly -- A Correct. Q -- and they missed the cardio -- the non- compaction? A Correct. Q And -- A Because they were so mild. Q Because they were so mild. A Exactly. Q Fair enough. Have you seen any evidence that the Ebstein’s -- the very mild Ebstein’s anomaly was causing him any issues prenatally? A No. Q Have you seen any evidence from treating him and his medical records that he developed non-immune hydrops as a result of the Ebstein’s anomaly? A No. He had no evidence of hydrops. Most importantly, when he was born he did not have skin edema, according to the history and physical by attending physician neonatologist. He also -- his chest x-ray at the original hospital did not show pulmonary edema and did not show pleural effusions. His echocardiogram on day one at Wolfson Children’s Hospital did not show a pericardial effusion. Hydrops fetalis is -- the non-immune hydrops that’s due to a heart condition is basically congestive heart failure. In order to diagnose hydrops you have to have multiple fluid collections. You have to have skin edema and/or one of the following three things. Or two of the following three things. Pleural effusion, pericardial effusion, ascites. They didn’t check for ascites so I don’t know about that. But I do know in his first day of life he did not have skin edema, according to the history of all the physicians who examined him. He did not have pleural effusion per the chest x-ray reports. And he did not have pericardial effusion according to the echo report. So he therefore did not have hydrops. Q Would a large -- well, would a loss of weight from 10.3 pounds to 8.7 be enough evidence to make a finding that he had had - A No. Q -- non-immune hydrops -- A No. Because you would lose weight from the acute tubular necrosis. As you recover from acute tubular necrosis, the injury to the kidneys, you go through a polyuric phase where you can actually diurese, get rid of the excess fluid. In fact, when I saw him on day six of life he was dry. I had to give him volume. Q And because he had to give him volume -- that’s fluids? A Right. Fluid volume. Yes. That was day six. But I’m just giving an example. I think he dried out. And that could be from the injury to the kidneys, which he had evidence of that by his creatinine going up after birth. Q And babies often lose weight after they’re born? A Oh yeah. Of course. They commonly lose up to 15 percent of their body weight in the first few days or week of life. Dr. Joyce readmitted Samuel to Wolfson’s on June 5, 2009, for initiation of cardiac medications and further diagnostic workup. While at Wolfson’s for this second hospital stay, his records reflect that he had a chest x-ray, a head ultrasound, an EEG, a head MRI, and ECGs. The results of the EEG were abnormal: IMPRESSION: This is an abnormal EEG because of excessive sharp waves, asynchrony, and excessive suppression. This would be consistent with encephalopathic process but is not specific with regard to etiology. Clinical correlation is advised. An MRI was also performed on June 8, 2009: IMPRESSION: Linear T1 hyperintensity in the region of the straight sinus, the totcula and the right sigmoid sinus is most likely the sequelle of recent birth although if there is clinical concern for sinus thrombosis, an MRV could be performed. Possible punctuate focus of intraparenchymal hemorrhage in the right frontal lobe. I personally discussed these findings with Dr. Ceron-Canas (primary care physician) on 6/9/09 at 11:45 hours. Dr. Joyce requested a neurology consultation during the second hospital stay. The consulting neurologist, Dr. Hammond, raised the issues of both Samuel’s risk of hypoxic ischemic brain injury, as well as a recommendation for genetics consultation due to Samuel’s dysmorphic features (“wide upper extremity polydactyly as well as suspected mild low-set ears.”). His hospital discharge summary dated June 8, 2009, reflect the following diagnoses: Diffuse non-Q wave myocardial infarction with secondary decreased ventricular systolic function, clinically improving. Neonatal jaundice exacerbated by recent neonatal polycythemia plus bruising from shoulder dystocia, improving. Possible hypoxic ischemic encephalopathy. Ebstein’s anomaly of the tricuspid valve. Mild dehydration, resolved. Samuel’s pediatrician, Dr. Miles, referred him for a neurology consult with Dr. Harry Abram, which took place when Samuel was approximately six months old. Dr. Abram noted “global delay” and made a referral for the parents to seek occupational, physical, and speech therapies for Samuel. He also recommended a genetics referral and careful monitoring for seizures, with a follow-up with neurology in six months. In May 2010, Samuel’s pediatrician, Dr. Miles, referred the Herefords to Dr. Anthony Perszyk, a geneticist with the University of Florida Pediatric Multispecialty Center. Noting Samuel’s history of hypotonia, polydactyly, and cardiomyopathy, Dr. Perszyk ordered lab work and genetics testing to begin to explore whether there was a genetic basis for Samuel’s impairments. Following this initial testing, Dr. Perszyk wrote to Dr. Miles in June 2010, regarding the test results, and stated in relevant part: Labs that we obtained at the end of May have now been completed. An extensive microarray or genetic analysis of the boy’s chromosomes is reported as within normal limits. There does not seem to be additional deletions or duplications of his chromosome material that accounts for hypotonia or developmental delay. Some specific regions would be on chromosome 17; this did not show up in the testing. There may be other tests we might do, but at the present time, this is adequate for ruling out many of the common disorders that give a child low muscle tone and developmental delays. Dr. Perszyk addressed Samuel’s possible seizure activity and wanted to follow up the following month. He also noted Samuel had been taken off some dietary supplements and wanted certain lab work to be repeated to determine its effect on mitochondrial function. Dr. Perszyk further noted that while Samuel was large for gestational age, he is close in weight to the Herefords’ other children. Dr. Perszyk saw Samuel again in July 2010, and again wrote a letter to Dr. Miles, which stated in relevant part: Previous genetic testing so far has not revealed a specific genetic abnormality. A DNA microarray testing as well as a metabolic testing have all been within normal limits. Initially fatty acid oxidation abnormalities were suspected with abnormality seen on initial screening laboratories. However, discontinuing the use of additional oils such as omega 3 or FISH oil has allowed his levels to improve amino acids from the urine, and plasma amino acids, are all within normal limits now at this time. Also acylcarnitine profile is improved with better utilization at the mitochondrial level of all his fatty acids. CK level is 55. While Dr. Perszyk noted that there may be consideration of additional DNA testing, he did not order it. Moreover, Mrs. Hereford recalls that Dr. Perzyk mentioned to them that an additional genetic test would cost $20,000, as insurance would not cover it. The record does not reflect any order for additional genetic testing from Dr. Perszyk. On February 1, 2011, Dr. Perszyk again saw Samuel and again wrote Dr. Miles regarding the office visit. Dr. Perszyk referenced Samuel’s significant visual problems and the need for ophthalmology examination. Again, he referenced “a plan to consider” further testing, including a video EEG, brain MRI and other DNA testing, but there is no reference to additional orders for genetic tests. Moreover, Mrs. Hereford credibly testified that “we did exactly what he asked us to do. I am not aware of anything that he says that you’re saying that he ordered that we did not do.” Samuel was admitted to Wolfson’s Children’s Hospital by Dr. Perszyk on February 21, 2011, for “workup for seizure disorder,” including brain MRI, video EEG, brain MRI spectroscopy, and lab tests. He again consulted with Dr. Abrams. The MRI report initially stated that other than sinus disease and prominent frontal extraaxial fluid, the MRI was otherwise normal. However, an addendum, stated, “The images were again reviewed. The patient has a history of grand mal seizure and [is] also on seizure medication. In this clinical context, the findings could represent diffuse global cortical atrophy with prominence of the sylvian fissure and lateral ventricles. However one-year followup recommended for continued assessment.” Samuel was discharged on February 24, 2011, with a prescription for seizure medication and vitamin B6. While it is not entirely clear from the record if any additional genetic testing was completed, Dr. Perszyk saw Samuel in May 2016, and wrote a letter in conjunction with the office visit addressed “To Whom it May Concern” regarding Samuel. This letter was written at the request of the Herefords, who were unfamiliar with the typical process for filing such claims, at the time they were making application for NICA benefits. The letter, which appears to summarize his care for Samuel over the years, states as follows: Samuel Hereford is a 6 year old male that I have followed since infancy. He has had long standing hypotonia and developmental delays since birth. Samuel has had abnormal reflexes and spasticity during the first several years of life. He has the clinical features of cerebral palsy. This has always been the main concern with Samuel since his hypotonia was recognized and therapy was begun. He had events around the time of delivery that would be the etiological basis of the cerebral palsy. This is documented in his medical record. As a geneticist, I have followed him and tested him for other causes for his hypotonia and did not find any other cause. He continues to grow slowly and has markedly delayed motor and language skills. His growth is also slow with weight and length near the bottom of the growth curves. Dr. Dawn Duss is a pediatric ophthalmologist and is Samuel’s treating ophthalmologist. She is board-certified in ophthalmology and completed fellowship training in the sub- specialty of pediatric ophthalmology. Dr. Duss first examined Samuel in 2014 to evaluate him for poor visual behavior, and reviewed his medical records. She diagnosed him with cortical visual impairment, which is abnormal visual behavior which cannot be explained by an anatomical deficit in the eyeball, so, she explained, that deficit has to be somewhere along the optic pathways or occipital lobe. She further explained that there is nothing pathognomic about cortical visual impairment. The anatomy of the eye does not reflect the level of visual behavior in the child. Dr. Duss explained that Samuel has poor visual attention. He cannot match a shape to a chart, he is unable to maintain visual attention for any amount of time, and he does not have depth perception. Dr. Duss has treated hundreds of children who have cortical visual impairment as a result of hypoxic ischemic events. According to Dr. Duss, a hypoxic ischemic event is the number one cause of cortical visual impairment. In reviewing Samuel’s medical records, Dr. Duss noted that his 2011 MRI revealed diffuse global cortical atrophy with prominence of a Sylvian fissure and lateral ventricles. Dr. Duss explained that diffuse cortical atrophy on an MRI is a very typical finding in cortical visual impairment caused by a hypoxic ischemic event. She further noted that the fact that this did not show up in earlier MRIs is typical in a hypoxic ischemic birth because the atrophy has to have time to develop after the traumatic event. It is Dr. Duss’ opinion that the hypoxic ischemic event that Samuel suffered at birth is the sole cause of Samuel’s visual impairments. NICA retained Dr. Donald Willis, a board-certified obstetrician specializing in maternal fetal medicine, who reviewed the medical records related to Samuel’s birth and subsequent development to determine whether Samuel sustained an injury to the brain or spinal cord caused by oxygen deprivation or mechanical injury in the course of labor, delivery, or resuscitation in the immediate post-delivery period. In a report dated May 9, 2014, Dr. Willis referenced relevant parts of Samuel’s records and stated in pertinent part: The mother presented to the hospital in active labor at 36 weeks gestational age. Cervical dilation was 8 cms. Amniotic fluid was clear. No fetal heart rate (FHR) monitor tracing during labor was available for review. There was no mention of suspected fetal distress during labor. Delivery was complicated by a shoulder dystocia with a six-minute delay in delivery. The baby was large-for-gestational age with a birth weight of 4,688 grams. An extra digit was noted on the right hand. The newborn was described as depressed, floppy and apnic at birth. Chest compressions were initiated. A heart rate of >100bpm was established by 90 seconds. Bag and mask ventilation was required for about two-minutes. Cord blood gas showed a pH of 7.22 and a base excess of only -2. The baby was taken to the NICU for evaluation. Nasal cannula oxygen was required for respiratory distress. A chest x-ray showed an enlarged heart. Muscle tone was decreased. The initial blood gas in the NICU was at about four hours of age. The pH was 7.35 with a base excess of -6. The baby was transferred to Baptist Hospital at six hours of age due to respiratory distress and an enlarged heart. Admission to Baptist Hospital indicated the baby was in critical and unstable condition. There was minimal muscle tone. Platelet count dropped to 88,000. Nasal cannula oxygen was required until DOL 3. Antibiotics were given, but cultures returned as no growth. Cardiac ECHO showed severe pulmonary hypertension and decreased ventricular function. No seizure activity was described. The baby was discharged on DOL 4. EEG on DOL 8 was abnormal and consistent with encephalopathy. MRI on the same day showed finding “most likely represents sequellae of recent birth trauma” with possible punctuate interparenchymal hemorrhage. Genetic evaluation was done due to an extra digit, hypotonia, cardiomyopathy at birth, visual cortical impairment, possible seizures and developmental delay. Chromosome analysis and microarray were normal. No specific genetic diagnosis was made. In summary, delivery was complicated by a shoulder dystocia that resulted in a depressed newborn, requiring chest compressions and bag and mask ventilation. Despite the initial depression with an Apgar score of only 3 at one minute, the baby’s condition improved with an Apgar score of 8 at five minutes. The newborn hospital course was complicated by respiratory distress, poor muscle tone, cardiomegaly and thrombocytopenia. EEG on DOL 8 was abnormal and consistent with encephalopathy. Based on the above history, some degree of oxygen deprivation at birth would be expected. However, the umbilical cord gas was normal (ph 7.22). Newborn depression at birth, severe enough to require cardiac compression would be unexpected with a cord pH of 7.22. It is likely the cord blood pH reflects the acid-base status of the fetus prior to the shoulder dystocia and not the actual status after delivery was completed six minutes later. This is reasonable since the blood flow through the umbilical cord ceases after the head is delivered. So for six minutes the baby was oxygen deprived, which may not be reflected in the blood cord gas findings. The other complicating issue is the possibility of an underlying genetic problem that could cause or contribute to the developmental delay. I am not aware of any specific diagnosis, but this issue could be better addressed by Pediatric Neurology. There was an obstetrical event (shoulder dystocia) that resulted in loss of oxygen to the baby’s brain during delivery. The oxygen deprivation resulted in brain injury. I am not able to comment about the extent of the injury. In a deposition on November 13, 2015, Dr. Willis further explained how shoulder dystocia causes oxygen deprivation. Once a baby’s head is delivered, the umbilical cord is compressed, so there is no real oxygen supply to the baby after the head is delivered until the delivery is completed. In Samuel’s case, the remainder of his body was delivered six minutes after his head, so he did not receive oxygen for that period of time. Additionally, because the medical records reflect that his first gasp was less than one minute and sustained respiration was in two minutes, it was likely that Samuel experienced more than six minutes of oxygen deprivation. Dr. Willis further explained with a shoulder dystocia, that the pH of the blood in the umbilical cord reflects what the baby’s acid-base status was just prior to delivery and not the acid-base status when the delivery is completed. Therefore, Samuel’s blood cord pH is not an accurate indicator of the pH following delivery with a shoulder dystocia. He described Samuel’s blood cord gas as “relatively normal” and that indicated the baby was not in distress prior to delivery. There were no fetal heart rate strips available for him to review. Samuel’s Apgar score was 3 at one minute and 8 at 5 minutes. Dr. Willis explained that the one-minute Apgar score tells what resuscitative measures may be necessary. The five- minute Apgar score tells more about the baby’s overall response and degree of hypoxia and acidosis. Samuel’s five-minute Apgar score of 8 is a normal score, and that the neurologic outcome of babies “is probably better reflected by the five-minute Apgar score, not the one-minute Apgar score, the long-term neurologic development.” However, when asked whether the MRI taken of Samuel on June 8, 2009, had findings with an acute hypoxic ischemic event, he replied “yes.” Specifically, he noted that the MRI report described punctuate or small pinpoint hemorrhages within the brain which is consistent with birth trauma. When asked whether the findings of the EEG taken on June 8, 2009, of excessive sharp waves, asynchrony, and excessive suppression is consistent with a hypoxic ischemic brain injury, he replied “yes.” It is Dr. Willis’s opinion that Samuel did sustain brain injury due to oxygen deprivation. He addressed the possible role of Samuel’s heart problems: A: Well, this baby had -- had birth defects, congenital heart defects, congenital birth defects. There was the enlarged heart, and the subsequent echoes after birth showed poor cardiac function. That was all present at birth. That was not something that developed after birth. The baby did have a sixth digit on the right hand, so there were birth defects present. And I guess where -- where I say any, you know, genetic diagnosis, there can also be just developmental abnormalities that can cause neurologic injury that may not have specific DNA probes to identify the defect or may not have a gross abnormality in the chromosomes. So what I’m trying to say is that this baby obviously had certain congenital birth defects, and I’m not sure if there were congenital birth defects that could have contributed to the oxygen deprivation to result in his eventual neurologic outcome. Q: Okay. Well, doctor, let me ask you about the poor cardiac function that you describe in the echocardiogram. Can that poor cardiac function that you see – and maybe this goes beyond the scope of your expertise, but that poor cardiac function could have been caused by damage to the heart tissue as a result of a hypoxic brain injury; correct? A: Well, I guess -- I guess that’s possible, but the baby -- we knew the baby had thick myocardial tissue prior to delivery, and that’s what was found after delivery so that’s a preexisting problem. That’s a congenital birth defect. Q: Now, babies that have those types of valves or the enlarged heart that you describe are born without problems all the time; correct? Mr. Bajalia: Objection to form. The witness: Well. I’m not -- I’m not sure how to answer that. I mean, we know babies with congenital heart defects have a higher incidence of neurologic problems. I mean, that -- that, we’ve known for some time. So I’m not sure. Maybe if you ask me that question again, I’ll try to answer. Mr. Nowak: Well, let me ask a little different, Doctor. You don’t have an opinion in this case one way or another as to what causes Sam -- caused Sam Hereford’s developmental delays, correct – A: Correct. Q:- -the congenital problem or the hypoxic brain -- the hypoxic brain event we’ve been talking about; correct? A: Correct. My – my review of the case – I am not asked to comment as to the severity of the injury, only if there was any brain injury due to hypoxia at birth. Q Okay. And you concluded that there was; correct? A Correct. Dr. Willis’ opinion that there was an apparent obstetrical event that resulted in loss of oxygen or mechanical trauma to the baby’s brain during labor, delivery or the immediate post-delivery period is credited. NICA also retained Dr. Michael Duchowny to evaluate Samuel. Dr. Duchowny is board-certified in pediatric neurology, with special qualifications in child neurology and in clinical neurophysiology. He is a senior staff attending at Nicklaus Children’s Hospital, and directs the neurology training program. Dr. Duchowny reviewed Samuel’s medical records and performed an independent medical examination on Samuel on June 18, 2014. In a medical report dated June 18, 2014, Dr. Duchowny stated the following: In Summary, Samuel’s neurological evaluation reveals evidence of global developmental delay which includes a substantial mental and motor impairment. He additionally manifests multiple dysmorphic features including midfacial compression, polydactyly, and a dysmorphic dental pattern. There is abundant self-stimulatory activity including blindisms and a lack of social interaction consistent with an autistic presentation. In contrast, there are no specific focal or lateralizing neurologic findings. Samuel’s medical records confirm his parent’s history of significant problems at birth. He was delivered at Memorial Hospital Jacksonville via delivery complicated by shoulder dystocia with the head [sic] being delivered 6 minutes later. The pregnancy had previously been complicated by macrosomia, polyhydramnios and left renal pyelectasis. Samuel was depressed at birth; a heart rate less than 100 was noted and he was floppy and apneic. The heart rate increased to 100 by 90 seconds of age and his Apgar score of 3 at 1 minute increased to 8 at 5 minutes. Cord blood gases were perfectly normal with a pH of 7.22 and base excess of -2. Samuel had significant cardiomegaly and had an in depth cardiac workup. He also suffered from respiratory distress, thrombocytopenia, and severe pulmonary hypertension. Of note, an MRI scan of the brain performed on June 8th revealed increased signal in the straight sinus and a punctate area of signal in the right frontal region. An EEG on the 8th day of life was consistent with encephalopathy. There was additional evidence of borderline polycythemia and hypoglycemia. Although Samuel has substantial mental and motor impairment, today’s evaluation and review of the medical records does not suggest that his neurological injury occurred in the course of labor or delivery. More likely, Samuel has neurological problems that were acquired prenatally and his delays are therefore likely to be on a developmental basis. For this reason, I am not recommending Samuel for compensation within the NICA program. Dr. Duchowny reaffirmed his opinions contained in his June 2014 written report when he was deposed on November 10, 2015. Dr. Duchowny agreed that Samuel suffered birth trauma and some degree of oxygen deprivation, but disagrees that the oxygen deprivation suffered by Samuel resulted in brain injury. Dr. Duchowny is of the opinion that none of the findings on the MRI are the cause of Samuel’s problems because the findings are small and would not be expected to produce the pattern of deficits that he has. Instead, Dr. Duchowny is of the opinion that Samuel’s deficits were acquired prenatally. To diagnose a hypoxic ischemic brain injury, Dr. Duchowny considers the history, lab and image findings, and physical examination. Regarding Samuel’s abnormal EEG, Dr. Duchowny noted that while that means there is abnormal brain function, the cause is essentially unknown based on the EEG findings. Further, Dr. Duchowny noted that Samuel’s five-minute Apgar score was 8, which typically would not be indicative of a severe hypoxic brain injury, and that while Samuel needed resuscitation, he appeared to respond to them by the five-minute Apgar determination. Overall, Dr. Duchowny is of the opinion that the clinical picture of Samuel following delivery is inconsistent with an encephalopathic process that was caused by hypoxic ischemic brain injury at the time of delivery. He described Samuel as having a “whole complex of findings, and one of them is prenatally acquired cerebral palsy, and that would include hypotonia, the hyporeflexia and the motor developmental delay, but additionally he has severe visual impairment, which, again I think is brain based.” As for Samuel’s heart issues, Dr. Duchowny agrees that Samuel suffered a myocardial injury. But he attributed that most likely to congenital cardiomyopathy and congenital valvular problems. When asked whether oxygen deprivation can cause the type of myocardial injury that Dr. Joyce was describing, he testified that he had never seen that but it was possible in theory, noting that he was not an expert in cardiology. Nancy Rodgers-Neame (Dr. Rodgers) is a board-certified neurologist and epilepsy specialist with sub-specialties in pediatric neurology and epilepsy. She is Director of the Florida Comprehensive Epilepsy and Seizure Disorders Center in Tampa, and Medical Director of Neurodiagnostics, at Florida Hospital, Tampa Bay Division. After reviewing Samuel’s medical records, letters from his treating physicians, and the reports of Dr. Willis and Dr. Duchowny, she stated her opinion in an affidavit dated January 19, 2016, as follows: It is my opinion that Samuel Hereford suffered a birth-related neurological injury, as defined by Section 766.302(2), Florida Statutes, as a result of shoulder that caused a period of oxygen deprivation during delivery which led to a hypoxic-ischemic event that resulted in brain damage to Samuel Hereford. Although there are multiple possible contributing factors to Samuel Hereford’s neurologic disability, including congenital complications and anomalies, it is my opinion that the hypoxic birth-related neurological injury suffered by Samuel Hereford is the primary cause of his neurologic disability and rendered him permanently and substantially mentally and physically impaired. Following this records review, she performed an independent medical examination and evaluation on Samuel on March 30, 2016. She is not one of Samuel’s treating physicians, but is an expert witness on behalf of Petitioners. In Dr. Rodgers opinion, Samuel was acidotic at birth. While she acknowledged that Samuel’s MRIs of his brain are not typical of someone who had suffered such an event, she noted that an MRI is not always going to show a structural injury that coordinates with the functional problems that the child has. She acknowledged that Samuel has dysmorphic features which were prenatally acquired. She characterized them as “minor” and noted that by the time children are six years old, their dysmorphic features have to do with the fact that they are “not getting adequate input from their brain to the rest of their body. So the fact that he is confined to -- essentially unable to walk and confined to a wheelchair is significant in that it is going to cause some changes to the musculature in the legs and the musculature in the face and the arms and everything else.” Dr. Rodgers is of the opinion that the hypoxic event at Samuel’s birth was a significant contributor to his neurologic disability. Moreover, she is of the opinion that it is impossible to tell what his physical and mental condition would have been had he not suffered the hypoxic ischemic event during birth. She noted that the results of the EEG performed on Samuel when he was eight days old, noting “an excessive number of sharp waves, asynchrony and successive suppression is most consistent with an hypoxic ischemic event.” NICA presented the testimony of Dr. Jay Goldsmith, a board-certified neonatologist who is licensed in Louisiana, Florida and Virginia. He is a full professor at Tulane University School of Medicine, has an active clinical practice, and has been practicing neonatology for approximately 40 years. After reviewing the medical records in this case, Dr. Goldsmith wrote a report dated March 25, 2016, and summarized his conclusions as follows: In summary, this young man had a difficult delivery, but also has signs of a pre- existing condition prior to birth. It is my opinion to a reasonable degree of medical probability that the events at delivery did not cause or contribute to his condition today. The events in the first few days of life do not meet the criteria for intrapartum hypoxic-ischemic encephalopathy (low Apgar scores at 5 minutes, severe acidosis in the cord blood gases, seizures, multiple system organ involvement, etc.) and the cardiomyopathy seen at birth was probably due to non-immune hydrops from some intra-uterine condition. The rapid recovery of the heart and huge weight loss in the first 4 days of life would support this opinion. Babies who are asphyxiated will usually have oliguria and gain weight over the first several days of life. Moreover, the dysmorphic features suggest an intra-uterine etiology. The MRIs also are not consistent with the patterns seen after hypoxia-ischemia (watershed pattern or basil ganglia injury). The traumatic findings in the brain imaging most often resolve without sequelae. Therefore it is my belief that Samuel does not qualify for compensation under the Florida NICA statute. Dr. Goldstein’s ultimate opinion is that Samuel suffered prenatally from a condition called non-immune hydrops, also known as hydrops fetalis. He explained that hydrops fetalis is not really a diagnosis but is “a symptom complex secondary to another diagnosis,” which in his opinion is the congenital heart defect of mild Ebstein’s anomaly. Non-immune hydrops is a collection of fluid around areas of the body, and the neonate loses the fluid (and weight) after good systolic function of the heart is reestablished. He is of the opinion that Samuel’s cardiomyopathy at birth was part of the process with the Epstein’s anomaly that caused him to suffer congestive heart failure in utero, which caused him to develop non-immune hydrops. He further explained that this process results in a lack of perfusion or oxygenation to Samuel’s organs, including his brain, and ultimately led to the development of brain damage. He acknowledged that Samuel suffered a myocardial infarction, but attributed it to congestive heart failure due to congenital heart defects. Dr. Goldsmith was of the opinion that the findings on Samuel’s MRI were not consistent with long-term neurological deficits. He acknowledged that Samuel was born floppy, apneic and depressed, but noted that his five-minute Apgar score was 8 and that “minutes to first gasp” was recorded as less than one minute. With respect to the blood gases, Dr. Goldstein is of the opinion that just because the baby had a shoulder dystocia and a six-minute head to body birth interval, that it does not necessarily mean that there is total obstruction of the umbilical cord. These opinions are in disagreement with Dr. Willis’ testimony regarding the blood gases or the cord compression. As is common in cases which involve a “battle of the experts,” all of the physicians testified credibly as to their individual medical opinions. Dr. Goldstein’s testimony was consistent with some opinions of the other doctors testifying in this case, and inconsistent with others. He appears to be the only doctor who believes that Samuel had hydrops. It was not noted on any ultrasound during Mrs. Hereford’s pregnancy and is not a diagnosis that was ever mentioned to the Herefords by any of Samuel’s many treating doctors. Dr. Joyce unequivocally testified that Samuel did not have hydrops. While he and Dr. Willis agreed that a five-minute Apgar score is not typical for a baby with acute birth asphyxia, they disagreed as to whether or not the cord compression for six minutes resulted in lack of oxygen to the infant. The ultimate opinions of the two pediatric neurologists are obviously in disagreement. As Dr. Duss testified, this case is not “clear cut.” There is no dispute that Samuel has permanent physical and mental impairments. There is no real dispute that Samuel had a traumatic birth and that he was deprived of oxygen for a period of time, which led to some brain injury. There is no real dispute that Samuel has some dysphormic features, albeit generally considered mild. The dispute centers on what, more likely than not, was the primary cause of Samuel’s impairments. That is, was the hypoxic ischemic event that occurred at Samuel’s birth the cause of his disabilities, or is it more likely than not that they were caused by a prenatally acquired congenital or genetic disorder acquired in utero. The undersigned finds the testimony of two of Samuel’s treating physicians, Dr. Joyce and Dr. Duss, in separate specialties to be compelling. That is, these two specialists testified credibly that the hypoxic ischemic event which occurred at birth was the primary cause of Samuel’s impairments. Dr. Duss’ testimony that a hypoxic ischemic event is the number one cause of cortical visual impairment was not rebutted. The greater weight of the evidence establishes through the opinions of Dr. Joyce and Dr. Duss, together with Dr. Rodgers, that there was an apparent obstetrical event that resulted in loss of oxygen to Samuel’s brain during delivery that resulted in brain injury, which rendered him permanently and substantially mentally and physically impaired.
The Issue Whether Ashley Villarreal has suffered an injury for which compensation should be awarded under the Florida Birth-Related Neurological Injury Compensation Plan, as alleged in the claim for compensation.
Findings Of Fact Preliminary matters Ashley Villarreal (Ashley) is the natural daughter of Roy Villarreal and Carmen Luna. She was born a live infant on January 2, 1989, at Bethesda Memorial Hospital in Palm Beach County, Florida, and her birth weight was 3090 grams. The physician delivering obstetrical services during the birth of Ashley was Allen Dinnerstein, M.D., who was, at all times material hereto, a participating physician in the Florida Birth-Related Neurological Injury Compensation Plan, as defined by Section 766.302(7), Florida Statutes. The birth of Ashley Villarreal At or about 4:15 p.m., January 2, 1989, Carmen Luna was admitted to Bethesda Memorial Hospital. At the time, Carmen Luna was in active labor, and Ashley was post term with a gestational age of 41 weeks. Otherwise, Carmen Luna's pregnancy had been without complication. External fetal monitoring was commenced at 4:50 p.m. and indicated that the fetal heart tone was sporadically within the 60 beat per minute level, with a slow return to baseline; a level sufficient to indicate occasional fetal bradycardia and fetal distress. 1/ This situation evidenced a need for surgical intervention, and at 5:20 p.m. Carmen Luna was taken to the operating room. Anesthesia commenced at 5:25 p.m., a cesarean section surgical procedure was commenced at 5:39 p.m., and Ashley was delivered at 5:44 p.m. The operative report reflects that the following occurred during the course of the procedure: . . . a transverse incision was made into the uterus releasing meconium stained fluid. The vertex was delivered and the baby suctioned with DeLee. A loop of cord over the neck was removed and the baby then delivered completely continually being suctioned as the cord was double clamped and severed and the infant given to the neonatologist for care . . . . The delivery records likewise reflect that Ashley had a blue appearance at delivery, the presence of meconium staining, and the following resuscitation measures: "Stimulation," "Bulb Suction," "DeLee Suction," "Mech Suction" and "Whiffs Oz." When delivered, Ashley presented Apgar scores of 6 at one minute and 8 at five minutes. These scores are a numerical expression of the condition of a newborn infant, and reflect the sum points gained on assessment of the heart rate, respiratory effort, muscle tone, reflex irritability, and color, with each category being assigned a score ranging from the lowest score of 0 through a maximum score of 2. As noted, at one minute, Ashley's Apgar score totaled 6, with respiratory effort and reflex irritability being graded at 2 each, heart rate and muscle tone being graded at 1 each, and color being graded at 0. At 5 minutes, Ashley's Apgar score totaled 8, with heart rate, respiratory effort and reflex irritability being graded at 2 each, and muscle tone and color at 1 each. Such total scores could be characterized by an obstetrician as "good." Pertinent to this case, color, heart rate and respiratory effort are primarily related to the cardiovascular system, and color is the least significant indicator of an infant's brain or neurological status at birth. The categories of reflex irritability and muscle tone are, however, neurological assessments, which offer the greatest insight into the neurological condition of an infant at birth. Ashley's Apgar scores relative to those categories which reflect neurological status at birth were collectively a total of 3 out of a possible 4 at both 1 and 5 minutes. Under the circumstances, Ashley's Apgar scores, either globally or discretely, fail to reflect a hypoxic event at birth. At 6:00 p.m., following delivery, Ashley was admitted to the neonatal intensive care unit due to respiratory distress, possibly secondary to meconium aspiration. Ashley was accorded extra oxygen, via oxygen hood, for two days, and her meconium aspiration was successfully treated with antibiotics. During her admission, no clinical observations were noted that one would typically expect in a child undergoing hypoxic encephalopathy, and no neurological consult was ordered. 2/ On January 7, 1989, Ashley was discharged as an apparently well baby. Subsequent developments On July 29, 1989, Ashley was seen by M. Arenstein, D.O., for a "well baby visit," and no abnormalities were noted; however, on September 6, 1989, Ashley was again seen by Dr. Arenstein at which time the parents expressed their concern regarding Ashley "not sitting up, crawling, etc." Consequently, Dr. Arenstein referred Ashley for a pediatric consult with Jeffrey Perelman, M.D. Ashley was seen by Dr. Perelman on September 19, 1989, and he diagnosed her as developmentally delayed, and ultimately referred her to David Ross, M.D., for a neurological evaluation. Dr. Ross saw Ashley on July 2, 1990, and concluded: The patient has some mild facial dysmorphism with developmental delay in all fields associated with an abnormal neurologic exam with persistence of postural reflexes and hyperreflexia. The spectrum of findings is consistent with mental retardation of a mild to moderate degree probably due to cerebral palsy. 3/ Dr. Ross' ultimate diagnosis was mental retardation, and he recommended that Ashley have a full evaluation, including "an image of the brain either with CT scan or MRI (an EEG, torch titers, chromosome analysis)." Ashley was referred in August 1990, for a CT brain scan and an EEG. The CT scan is a neuroimaging study which can identify structural brain abnormalities occasioned by an hypoxic insult, as well as other causes. The EEG is a device used to detect abnormalities of the electrical currents of the brain such as seizure activity, which is often a manifestation of hypoxic insult at birth, and the death of neuronal cells. Here, both the CT scan and EEG were within normal limits. Ashley continued to be treated by Dr. Perelman through June 1991; however, on August 14, 1991, she came under the care of Miguel Simo, M.D., another pediatrician, because the parents were apparently dissatisfied with Dr. Perelman. Upon examination, Dr. Simo diagnosed Ashley as developmentally delayed, and referred her to Laszlo Mate', M.D., a physician practicing child neurology, for evaluation. Dr. Mate' examined Ashley on August 29, 1991, and observed: . . . a small, dysmorphic female in no apparent distress. Her head circumference is 47 cm which is in the 25th percentile. She doesn't have any neurocutaneous abnormalities. Her palmer creases are somewhat abnormal, but not of simian nature. Her fingers are slightly abnormal, extra long, and she seems to have a proximal displacement of both thumbs. Her ears are malformed with very small earlobes. The ears are somewhat posterior rotated and low set. Her eyes are almond shape but in view of her Indian heritage, that's probably normal. Both parents seem to have similar shaped eyes. The child has a somewhat prominent nose. The mouth is somewhat fishmouth in character and she has fairly shallow temporal area. She doesn't have any eyelashes on her lower eyelid. Dr. Mate's impression was: This is a markedly abnormal child with a developmental quotient in the 30's. She's currently is 30 months old and she functions around a 9-10 month level. She has multiple minor malformations which made the diagnosis of cerebral palsy somewhat unlikely. I suspect we are dealing with some prenatal etiology, either genetic or pregnancy related. 4/ Dr. Simo also referred Ashley for an MRI of the brain. An MRI, as with a CT scan, is a neuroimaging study which can identify structural abnormalities occasioned by hypoxic insult, as well as other causes. The MRI, performed September 20, 1991, was abnormal, evidencing "poor and decreased white matter myelinization extending to the frontal, occipital, and parietal cortex and decrease in white matter content in the centrum semiovale." Such damage could be reflective of birth asphyxia, developmental immaturity of the brain, or a myriad of other causes. Finally, Dr. Simo referred Ashley to Oscar Febles, M.D., a physician practicing genetics. Dr. Febles examined Ashley on November 1, 1991, and rendered a diagnosis of "psychomotor retardation of unknown etiology." Concluding, Dr. Febles observed: The clinical findings in this patient are not diagnostic of a particular genetic syndrome . . . In conclusion, this patient presents a clinical picture characterized by psychomotor retardation that cannot be diagnosed on the clinical findings and/or testing done. The fact that she presents diffuse demyelinization on the MRI would favor the diagnosis of cerebral palsy and/or a CNS degenerative disease. It is my recommendation that an MRI be repeated in approximately 6 months to see if the demyelinization process of the cortex previously seen is progressive or static. If found to be progressive it would indicate a CNS degenerative disease (e.g. leukodystrophies) and if static the diagnosis of cerebral palsy is most likely. In addition, it is also recommended . . . Genetic re-evaluation in 1 year. Whether, consistent with Dr. Febles' recommendation, an MRI was repeated or Ashley had a subsequent genetic re- evaluation does not appear of record. Notably, however, while Ashley was genetically tested and found to have a normal karyotype, such test does not rule out the preponderance of genetic disorders which manifest themselves in microscopic point mutations within a chromosome as opposed to total chromosomal malformation. The medical experts at hearing As to whether Ashley had sustained permanent and substantial mental and physical impairment as a result of an injury to her brain resulting from oxygen deprivation during the course of labor, delivery or resuscitation in the immediate post-delivery period, petitioners offered the testimony of Dr. David Ross, who, although a board certified neurologist, does not regularly treat neonates. Dr. Ross examined Ashley on July 2, 1990, and March 2, 1994. It was Dr. Ross' opinion that Ashley suffered a substantial and permanent mental and physical impairment as a consequence of oxygen deprivation during the course of labor and delivery. Compared with the opinion of Dr. Ross, the respondent offered the testimony of Dr. Michael Duchowny. Dr. Duchowny is a child neurologist who is board certified in pediatrics, neurology with special competence in child neurology and clinical neurophysiology. Dr. Duchowny is associated with the department of neurology at Miami Children's Hospital and routinely treats neonates suspected of having suffered a hypoxic event at birth. Dr. Duchowny examined Ashley on September 21, 1992, as well as observed her at hearing, and was familiar, as was Dr. Ross, with the pertinent medical records. It was Dr. Duchowny's opinion that Ashley was substantially and permanently mentally impaired, but that her physical impairment could best be described as mild to moderate. As to causation, it was Dr. Duchowny's opinion that the cause (etiology) of Ashley's mental and physical impairment (neurologic syndrome) was a developmental problem of in utero (prenatal) or genetic origin, and that any fetal distress she may have suffered at birth was not substantial and did not contribute to her condition. [Tr. 97] Here, I accept the testimony and opinion of Dr. Duchowny as being the more credible and substantial as to whether Ashley sustained a substantial and permanent mental and physical impairment, and the cause of such dysfunction. Dr. Duchowny's opinions are credible, supported by the observations of other physicians as heretofore noted, and are most consistent with conclusions to be drawn or inferences raised by the medical records received into evidence.
Findings Of Fact Xavier Concepcion was born on September 16, 2014, at Memorial Hospital West in Pembroke Pines, Florida. NICA retained Donald C. Willis, M.D. (Dr. Willis), to review Xavier’s medical records. In a medical report dated January 20, 2016, Dr. Willis made the following findings and expressed the following opinion: In summary, labor was complicated by maternal infection (chorioamnionitis) and a non- reassuring FHR pattern prior to birth. The baby was depressed at birth with a cord blood pH of <6.9. Seizure activity developed shortly after birth. MRI was consistent with acute brain infarction. There was an apparent obstetrical event that resulted in loss of oxygen to the baby’s brain during labor, delivery and continuing into the immediate post delivery period. It is possible the brain injury from oxygen deprivation was worsened by infection. I am unable to comment about the severity of the brain injury. Dr. Willis’ opinion that there was an obstetrical event that resulted in loss of oxygen to the baby’s brain during labor, delivery and continuing into the immediate post delivery period is credited. Respondent retained Michael Duchowny, M.D. (Dr. Duchowny), a pediatric neurologist, to evaluate Xavier. Dr. Duchowny reviewed Xavier’s medical records, and performed an independent medical examination on him on May 25, 2016. Dr. Duchowny made the following findings and summarized his evaluation as follows: Motor examination reveals symmetric muscle strength, bulk and tone. There are no adventitious movements and no focal weakness or atrophy. Xavier does not evidence dystonic postures or hypertonicity. He has full range of motion at all joints. Coordination: Xavier walks in a stable fashion and does not fall. He can arise from the floor without difficulty. His balance is good and he has well-developed axial and peripheral balance. He grasps with both hand[s] and moved objects between hands without difficulty. He did not fall and his head control is good. * * * In Summary, Xavier’s neurological examination discloses no significant findings. He is developmentally appropriate with no focal or lateralizing features to suggest a structural brain abnormality. Review of the medical records reveals that Xavier was born at Memorial West Hospital at term and transferred to Joe DiMaggio Children’s Hospital. Maternal membranes were ruptured 30 hours prior to delivery, and maternal chorioamnionitis and fever were treated with penicillin. Xavier was born vaginally and was pale, cyanotic, flaccid and unresponsive. A tight nuchal cord was removed. He weighed 7 pounds 7 ounces and his Apgar scores were 1, 5 and 7 at one, five, and ten minutes. The records indicated that an initial arterial pH was 6.95 but the base excess was unknown. Xavier was intubated at 3 minutes of age, established spontaneous respiration at 25 minutes of age and was subsequently extubated. His CBC revealed a bandemia of 22 on September 22nd. Seizures were noted on the first day of life and there was evidence of a mild coagulopathy. The placenta was positive for E.coli. An MRI scan of the brain revealed multiple acute infarcts in the left temporal, occipital and superior parietal regions and right thalamus and putamen, and a small subdural hematoma. Despite Xavier’s difficulties at birth, he has developed well and does not evidence neurodevelopmental delay. I am therefore not recommending Xavier for compensation within the NICA program. In order for a birth-related injury to be compensable under the Plan, the injury must meet the definition of a birth- related neurological injury and the injury must have caused both permanent and substantial mental and physical impairment. Dr. Duchowny’s opinion that Xavier has developed well and does not evidence neurodevelopmental delay is credited. A review of the file in this case reveals that there have been no expert opinions filed that are contrary to the opinion of Dr. Duchowny that Xavier has developed well and does not evidence neurodevelopmental delay. There is nothing in Dr. Duchowny’s report that indicates that Xavier has either a substantial mental or physical impairment. Thus, Xavier does not meet the requirement of having a substantial physical or mental impairment.
Findings Of Fact Dontae Bess, Jr., was born on July 21, 2011, at Lakeland Regional Medical Center in Lakeland, Florida. NICA retained Donald C. Willis, M.D. (Dr. Willis), to review Dontae’s medical records. In a medical report dated August 19, 2016, Dr. Willis made the following findings and expressed the following opinion: Spontaneous vaginal delivery was without difficulty. Birth weight was 3,220 grams. The baby was not depressed. Apgar scores were 9/9. No resuscitation was required at birth. The baby went to the normal newborn nursery and had an uncomplicated newborn hospital course with discharge on DOL 2. The child had developmental delays. MRI was done at 5 years of age and was “unremarkable.” In summary, pregnancy was induced for hypertension at term. There was no fetal distress during labor and the baby was not depressed at birth. The newborn hospital course was benign. MRI at 5 years of age did not suggest brain injury. There was no apparent obstetrical event that resulted in loss of oxygen or mechanical trauma to the baby’s brain or spinal cord during labor, delivery or the immediate post delivery period. Dr. Willis reaffirmed his opinion in an affidavit dated January 26, 2017. Dr. Willis’ opinion that there was no obstetrical event that resulted in loss of oxygen or mechanical trauma to the baby’s brain or spinal cord during labor, delivery or in the immediate post-delivery period is credited. Respondent retained Laufey Y. Sigurdardottir, M.D. (Dr. Sigurdardottir), a pediatric neurologist, to evaluate Dontae. Dr. Sigurdardottir reviewed Dontae’s medical records, and performed an independent medical examination on him on September 21, 2016. Dr. Sigurdardottir made the following findings and summarized her evaluation as follows: Summary: Dontae is a 5-year 2-month-old African-American male who is brought to the visit for an independent medical examination on his developmental delays. On review of his prenatal and birth history, I do not see any evidence of a likely hypoxic injury. He was born healthy and had no complications in the immediate postnatal period. He has then progressed to have mild gross motor delay and a quite significant language delay, although he is at this time in a regular education kindergarten. Neuroimaging did not show evidence of significant ischemic injury. Result as to question 1: The patient is found to have no substantial physical impairment, but to have a substantial language impairment at this time. Results as to question 2: There is no evidence in the medical record review of a substantial hypoxic event during labor or delivery, the infant had no signs of an encephalopathy in the immediate post natal period and no evidence of ischemic injury on neuroimaging. His language delay is not felt to be birth-related. Results as to question 3: Dontae’s prognosis for life expectancy is excellent and for full recovery is good. In light of the above-mentioned details and the lack of any evidence to suggest a birth related hypoxic injury, I do not recommend Dontae being included in the Neurologic Injury Compensation program, and I would be happy to answer additional questions. Dr. Sigurdardottir reaffirmed her opinions in an affidavit dated January 20, 2017. In order for a birth-related injury to be compensable under the Florida Birth-Related Neurological Injury Compensation Plan (Plan), the injury must meet the definition of a birth- related neurological injury and the injury must have caused both permanent and substantial mental and physical impairment. Dr. Sigurdardottir’s opinion that while Dontae has a substantial language impairment, he has no substantial physical impairment, is credited. A review of the file in this case reveals that there have been no expert opinions filed that are contrary to the opinion of Dr. Sigurdardottir that Dontae does not have a substantial physical impairment.
