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Dive into the research topics where Sarah B. Mulkey is active.

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Featured researches published by Sarah B. Mulkey.


Pediatrics | 2016

High-Dose Erythropoietin and Hypothermia for Hypoxic-Ischemic Encephalopathy: A Phase II Trial

Yvonne W. Wu; Amit Mathur; Taeun Chang; Robert C. McKinstry; Sarah B. Mulkey; Dennis E. Mayock; Krisa P. Van Meurs; Elizabeth E. Rogers; Fernando F. Gonzalez; Bryan A. Comstock; Sandra E. Juul; Michael E. Msall; Sonia L. Bonifacio; Hannah C. Glass; An N. Massaro; Lawrence Dong; Katherine W. Tan; Patrick J. Heagerty; Roberta A. Ballard

OBJECTIVE: To determine if multiple doses of erythropoietin (Epo) administered with hypothermia improve neuroradiographic and short-term outcomes of newborns with hypoxic-ischemic encephalopathy. METHODS: In a phase II double-blinded, placebo-controlled trial, we randomized newborns to receive Epo (1000 U/kg intravenously; n = 24) or placebo (n = 26) at 1, 2, 3, 5, and 7 days of age. All infants had moderate/severe encephalopathy; perinatal depression (10 minute Apgar <5, pH <7.00 or base deficit ≥15, or resuscitation at 10 minutes); and received hypothermia. Primary outcome was neurodevelopment at 12 months assessed by the Alberta Infant Motor Scale and Warner Initial Developmental Evaluation. Two independent observers rated MRI brain injury severity by using an established scoring system. RESULTS: The mean age at first study drug was 16.5 hours (SD, 5.9). Neonatal deaths did not significantly differ between Epo and placebo groups (8% vs 19%, P = .42). Brain MRI at mean 5.1 days (SD, 2.3) showed a lower global brain injury score in Epo-treated infants (median, 2 vs 11, P = .01). Moderate/severe brain injury (4% vs 44%, P = .002), subcortical (30% vs 68%, P = .02), and cerebellar injury (0% vs 20%, P = .05) were less frequent in the Epo than placebo group. At mean age 12.7 months (SD, 0.9), motor performance in Epo-treated (n = 21) versus placebo-treated (n = 20) infants were as follows: Alberta Infant Motor Scale (53.2 vs 42.8, P = .03); Warner Initial Developmental Evaluation (28.6 vs 23.8, P = .05). CONCLUSIONS: High doses of Epo given with hypothermia for hypoxic-ischemic encephalopathy may result in less MRI brain injury and improved 1-year motor function.


Pediatric Neurology | 2010

Nerve Root Enhancement on Spinal MRI in Pediatric Guillain-Barré Syndrome

Sarah B. Mulkey; Charles M. Glasier; Bassem El-Nabbout; William D. Walters; Christian Ionita; Michael McCarthy; Gregory B. Sharp; Rolla M. Shbarou

Guillain-Barré syndrome diagnosis is based on clinical presentation and supportive diagnostic testing. In its early stage, no single, reliable diagnostic test is available. However, a finding of nerve root enhancement on spinal magnetic resonance imaging may be useful. We evaluated the frequency of nerve root enhancement on spinal magnetic resonance imaging in children with Guillain-Barré syndrome. At a single tertiary pediatric center, we conducted a retrospective chart review of children with Guillain-Barré syndrome who had complete spinal or lumbosacral spinal magnetic resonance imaging with gadolinium administration from January 2002-January 2009. Twenty-four consecutive patients were identified. Spinal nerve root enhancement with gadolinium was present in 92% (22/24) of children with Guillain-Barré syndrome on initial spinal magnetic resonance imaging (95% confidence interval, 0.745-0.978). This finding increased to 100% of patients, after two patients underwent repeat spinal magnetic resonance imaging that did reveal nerve root enhancement. Patterns of enhancement were variable, but involved the thoracolumbar nerve roots in all patients. Enhancement of nerve roots with gadolinium on initial spinal magnetic resonance imaging was frequently present in these children with Guillain-Barré syndrome. Spinal magnetic resonance imaging is a sensitive diagnostic test and should be considered an additional diagnostic tool in select cases.


Pediatric Neurology | 2014

White Matter Injury in Newborns With Congenital Heart Disease: A Diffusion Tensor Imaging Study

Sarah B. Mulkey; Xiawei Ou; Raghu H. Ramakrishnaiah; Charles M. Glasier; Christopher J. Swearingen; Maria S. Melguizo; Vivien L. Yap; Michael L. Schmitz; Adnan T. Bhutta

BACKGROUND Brain injury is observed on cranial magnetic resonance imaging preoperatively in up to 50% of newborns with congenital heart disease. Newer imaging techniques such as diffusion tensor imaging provide sensitive measures of the white matter integrity. The objective of this study was to evaluate the diffusion tensor imaging analysis technique of tract-based spatial statistics in newborns with congenital heart disease. METHODS Term newborns with congenital heart disease who would require surgery at less than 1 month of age were prospectively enrolled (n = 19). Infants underwent preoperative and postoperative brain magnetic resonance imaging with diffusion tensor imaging. Tract-based spatial statistics, an objective whole-brain diffusion tensor imaging analysis technique, was used to determine differences in white matter fractional anisotropy between infant groups. Term control infants were also compared with congenital heart disease infants. Postmenstrual age was equivalent between congenital heart disease infant groups and between congenital heart disease and control infants. RESULTS Ten infants had preoperative brain injury, either infarct or white matter injury, by conventional brain magnetic resonance imaging. The technique of tract-based spatial statistics showed significantly lower fractional anisotropy (P < 0.05, corrected) in multiple major white matter tracts in the infants with preoperative brain injury compared with infants without preoperative brain injury. Fractional anisotropy values increased in the white matter tracts from the preoperative to the postoperative brain magnetic resonance imaging correlating with brain maturation. Control infants had higher fractional anisotropy in multiple white matter tracts compared with infants with congenital heart disease. CONCLUSION Tract-based spatial statistics is a valuable diffusion tensor imaging analysis technique that may have better sensitivity in detecting white matter injury compared with conventional brain magnetic resonance imaging in term newborns with congenital heart disease.


Epilepsia | 2017

Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H

Sarah B. Mulkey; Bruria Ben-Zeev; Joost Nicolai; John L. Carroll; Sabine Grønborg; Yong-hui Jiang; Nishtha Joshi; Megan L. Kelly; David A. Koolen; Mohamad A. Mikati; Kristen Park; Phillip L. Pearl; Ingrid E. Scheffer; Rebecca C. Spillmann; Maurizio Taglialatela; Silvia Vieker; Sarah Weckhuysen; Edward C. Cooper; Maria Roberta Cilio

To analyze whether KCNQ2 R201C and R201H variants, which show atypical gain‐of‐function electrophysiologic properties in vitro, have a distinct clinical presentation and outcome.


Journal of Child Neurology | 2014

Advancing Neurologic Care in the Neonatal Intensive Care Unit With a Neonatal Neurologist

Sarah B. Mulkey; Christopher J. Swearingen

Neonatal neurology is a growing subspecialty area. Given the considerable amount of neurologic problems present in the neonatal intensive care unit, a neurologist with expertise in neonates is becoming more important. We sought to evaluate the change in neurologic care in the neonatal intensive care unit at our tertiary care hospital by having a dedicated neonatal neurologist. The period post–neonatal neurologist showed a greater number of neurology consultations (P<.001), number of neurology encounters per patient (P<.001), a wider variety of diagnoses seen, and an increase in the use of video electroencephalography (P=.022), compared to the period pre–neonatal neurologist. The neonatologists expressed appreciation for having a dedicated neurologist available. Standardized protocols for treating hypoxic-ischemic encephalopathy and neonatal seizures were also developed. Overall, by having a neonatal neurologist, neurology became part of the multidisciplinary team providing focused neurologic care to newborns.


The Journal of Pediatrics | 2017

Erythropoietin and Brain Magnetic Resonance Imaging Findings in Hypoxic-Ischemic Encephalopathy: Volume of Acute Brain Injury and 1-Year Neurodevelopmental Outcome

Sarah B. Mulkey; Raghu H. Ramakrishnaiah; Robert C. McKinstry; Taeun Chang; Amit Mathur; Dennis E. Mayock; Krisa P. Van Meurs; G. Bradley Schaefer; Chunqiao Luo; Shasha Bai; Sandra E. Juul; Yvonne W. Wu

&NA; In the Neonatal Erythropoietin and Therapeutic Hypothermia Outcomes study, 9/20 erythropoietin‐treated vs 12/24 placebo‐treated infants with hypoxic‐ischemic encephalopathy had acute brain injury. Among infants with acute brain injury, the injury volume was lower in the erythropoietin than the placebo group (P = .004). Higher injury volume correlated with lower 12‐month neurodevelopmental scores. Trial registration ClinicalTrials.gov: NCT01913340.


Epilepsia | 2016

Rapid and safe response to low-dose carbamazepine in neonatal epilepsy.

Tristan T. Sands; Martina Balestri; Giulia Bellini; Sarah B. Mulkey; Olivier Danhaive; Eliza Hayes Bakken; Maurizio Taglialatela; Michael S. Oldham; Federico Vigevano; Gregory L. Holmes; Maria Roberta Cilio

To evaluate treatment responses in benign familial neonatal epilepsy (BFNE).


Pediatric Radiology | 2015

Brain ketones detected by proton magnetic resonance spectroscopy in an infant with Ohtahara syndrome treated with ketogenic diet.

Kim M. Cecil; Sarah B. Mulkey; Xiawei Ou; Charles M. Glasier

Atypical resonances on proton magnetic resonance spectroscopy (MRS) examinations are occasionally found in children undergoing a metabolic evaluation for neurological conditions. While a radiologist’s first instinct is to suspect a pathological metabolite, usually the origin of the resonance arises from an exogenous source. We report the appearance of distinct resonances associated with a ketogenic diet in a male infant presenting with Ohtahara syndrome. These resonances can be confused in interpretation with lactate and glutamate. To confirm assignments, the basis set for quantification was supplemented with simulations of β-hydroxybutyrate, acetone and acetoacetate in LCModel spectroscopy processing software. We were able to quantitate the levels of end products of a ketogenic diet and illustrate how to distinguish these resonances.


Pediatric Neurology | 2018

Neuroimaging Findings in Normocephalic Newborns With Intrauterine Zika Virus Exposure

Sarah B. Mulkey; Gilbert Vezina; Dorothy I. Bulas; Zarir Khademian; Anna Blask; Youssef Kousa; Caitlin Cristante; Lindsay Pesacreta; Adré J. du Plessis; Roberta L. DeBiasi

BACKGROUND Congenital Zika infection can result in a spectrum of neurological abnormalities in the newborn. Newborns exposed to Zika virus in utero often have neuroimaging as part of their clinical evaluation. METHODS Through the Congenital Zika Program at Childrens National Health System in Washington DC, we performed fetal or neonatal neuroimaging, including magnetic resonance imaging and ultrasound, on over 70 fetuses or neonates with intrauterine Zika exposure. Novel findings on neonatal brain magnetic resonance imaging were observed in two instances. RESULTS Gadolinium-contrast magnetic resonance imaging showed enhancement of multiple cranial nerves at three days of age on one infant. Another infant underwent magnetic resonance imaging at 16 days of age and was shown to have a chronic ischemic cerebral infarction. This infant had previously normal fetal magnetic resonance imaging. CONCLUSION Cranial nerve enhancement and cerebral infarction may be among the expanding list of neurological findings in congenital Zika infection. Postnatal brain magnetic resonance imaging should be considered for newborns exposed to Zika virus in utero.


American Journal of Neuroradiology | 2014

Impaired white matter development in extremely low-birth-weight infants with previous brain hemorrhage.

Xiawei Ou; Charles M. Glasier; Raghu H. Ramakrishnaiah; Sarah B. Mulkey; Zhaohua Ding; Teresita L. Angtuaco; Aline Andres; Jeffrey R. Kaiser

BACKGROUND AND PURPOSE: Brain hemorrhage is common in premature infants. The purpose of the study is to evaluate white matter development in extremely low-birth-weight infants with or without previous brain hemorrhage. MATERIALS AND METHODS: Thirty-three extremely low-birth-weight infants were prospectively enrolled and included in this institutional review board–approved study. Another 10 healthy term infants were included as controls. The medical records of the extremely low-birth-weight infants were reviewed for sonography diagnosis of intraventricular hemorrhage. All infants had an MR imaging examination at term-equivalent age for detection of previous hemorrhage, and their white matter was scored and compared among different groups. DTI measured fractional anisotropy values were also compared voxelwise by tract-based spatial statistics. RESULTS: Compared with controls, the white matter score was not significantly different in extremely low-birth-weight infants without blood deposition on MR imaging (P = .17), but was significantly worse in extremely low-birth-weight infants with blood deposition on MR imaging but no intraventricular hemorrhage diagnosis by sonography (P = .02), in extremely low-birth-weight infants with grade 1 or 2 intraventricular hemorrhage on sonography (P = .003), and in extremely low-birth-weight infants with grade 3 or 4 intraventricular hemorrhage on sonography (P = .0001). Extremely low-birth-weight infants without blood deposition on MR imaging did not show any white matter regions with significantly lower fractional anisotropy values than controls. Extremely low-birth-weight infants with blood deposition on MR imaging, but no intraventricular hemorrhage diagnosis, did show white matter regions with significantly lower fractional anisotropy values, and extremely low-birth-weight infants with intraventricular hemorrhage diagnosis had widespread white matter regions with lower fractional anisotropy values. CONCLUSIONS: Previous brain hemorrhage is associated with abnormal white matter in extremely low-birth-weight infants at term-equivalent age, and sonography is not sensitive to minor hemorrhages that are sufficient to cause white matter injury.

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Adré J. du Plessis

George Washington University

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Charles M. Glasier

University of Arkansas for Medical Sciences

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Raghu H. Ramakrishnaiah

University of Arkansas for Medical Sciences

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Christopher J. Swearingen

University of Arkansas for Medical Sciences

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Jeffrey R. Kaiser

Baylor College of Medicine

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Roberta L. DeBiasi

George Washington University

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Xiawei Ou

University of Arkansas for Medical Sciences

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Dorothy I. Bulas

Children's National Medical Center

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Gilbert Vezina

Children's National Medical Center

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