Elliot Walters

Dr. Elliot Walters


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 December 2010 in Synapse
Verified
Journal Article
Open access
PDF file
LMLisa McFadden
Lisa McFadden
AHAmanda J. Hoonakker
Amanda J. Hoonakker
PVPaula L. Vieira‐Brock
Paula L. Vieira‐Brock
KSKristen Stout
Kristen Stout
NSNicole M. Sawada
Nicole M. Sawada
AFAnnette E. Fleckenstein
Annette E. Fleckenstein
Administration of high doses of methamphetamine (METH) causes persistent dopaminergic deficits in both nonhuman preclinical models and METH‐dependent persons. Noteworthy, adolescent [i.e., postnatal day (PND) 40] rats are less susceptible to this damage than young adult (PND90) rats. In addition, biweekly treatment with METH, beginning at PND40 and continuing throughout development, prevents the persistent dopaminergic deficits caused by a “challenge” high‐dose METH regimen when administered at PND90. Mechanisms underlying this “resistance” were thus investigated. Results revealed that biweekly METH treatment throughout development attenuated both the acute and persistent deficits in VMAT2 function, as well as the acute hyperthermia, caused by a challenge METH treatment. Pharmacokinetic alterations did not appear to contribute to the protection afforded by the biweekly treatment. Maintenance of METH‐induced hyperthermia abolished the protection against both the acute and persistent VMAT2‐associated deficits suggesting that alterations in thermoregulation were caused by exposure of rats to METH duringdevelopment. These findings suggest METH during development prevents METH‐induced hyperthermia and the consequent METH‐related neurotoxicity. Synapse 2011.

26 September 2022 in The American Journal of Surgery
Verified
Journal Article
Closed access
JDJana E DeJesus
Jana E DeJesus
NSNikhil R. Shah
Nikhil R. Shah
CFCamila Franco-Mesa
Camila Franco-Mesa
EWElliot Walters
Elliot Walters
APAlen Palackic
Alen Palackic
Steven Eric WolfSteven Eric Wolf
Steven Eric Wolf

1 September 2019 in Archives of Plastic Surgery
Verified
Journal Article
Open access
PDF file
CBCara K Black
Cara K Black
EZElizabeth G Zolper
Elizabeth G Zolper
EWElliot Walters
Elliot Walters
JWJessica Wang
Jessica Wang
JMJesus Martinez
Jesus Martinez
KEKaren K Evans
Karen K Evans
Background Incisional hernia is a common complication following visceral organ transplantation. Transplant patients are at increased risk of primary and recurrent hernias due to chronic immune suppression and large incisions. We conducted a retrospective review of patients with a history of liver or kidney transplantation who underwent hernia repair to analyze outcomes and hernia recurrence. Methods This is a single center, retrospective review of 19 patients who received kidney and/or liver transplantation prior to presenting with an incisional hernia from 2011 to 2017. All hernias were repaired with open component separation technique (CST) with biologic mesh underlay. Results The mean age of patients was 61.0±8.3 years old, with a mean body mass index of 28.4±4.8 kg/m2, 15 males (78.9%), and four females (21.1%). There were seven kidney, 11 liver, and one combined liver and kidney transplant patients. The most common comorbidities were hypertension (16 patients, 84.2%), diabetes (9 patients, 47.4%), and tobacco use (8 patients, 42.1%). Complications occurred in six patients (31.6%) including hematoma (1/19), abscess (1/19), seroma (2/19), and hernia recurrence (3/19) at mean follow-up of 28.7±22.8 months. With the exception of two patients with incomplete follow-up, all patients healed at a median time of 27 days. Conclusions This small, retrospective series of complex open CST in transplant patients shows acceptable rates of long-term hernia recurrence and healing. By using a multidisciplinary approach for abdominal wall reconstruction, we believe that modified open CST with biologic mesh is a safe and effective technique in the transplant population with complex abdominal hernias.

9 May 2019 in Clinics in Podiatric Medicine and Surgery
Verified
Journal Article
Closed access
VKVikas S. Kotha
Vikas S. Kotha
KRKevin Ragothaman
Kevin Ragothaman
EWElliot Walters
Elliot Walters
CAChristopher E. Attinger
Christopher E. Attinger
JSJohn S. Steinberg
John S. Steinberg

8 November 2024 in European Burn Journal
Verified
Journal Article
Open access
PDF file
SMSheldon A. McCown
Sheldon A. McCown
EWElliot Walters
Elliot Walters
APAlen Palackic
Alen Palackic
CFCamila Franco-Mesa
Camila Franco-Mesa
ADAshton Davis
Ashton Davis
Steven Eric WolfSteven Eric Wolf
Steven Eric Wolf
Background: Diabetic patients often present with complex limb pathology, resulting in impaired sensation in the distal extremities making tactile injuries such as burns difficult to notice. We posit that poorly controlled diabetes mellitus, evidenced by increasing elevations in hemoglobin A1c, is associated with delayed wound healing and increased complications in burn patients. Methods: The TriNetX Network, a database of 89 million patients across the U.S., was queried for diabetic patients with foot and ankle burns. Patients were divided into four groups based on A1c: properly controlled (9%), and propensity-matched non-diabetic controls. Evaluated outcomes included split-thickness skin grafting, infections, amputations, acute kidney failure (AKF), and mortality within one month of the burn. Results: When comparing the poorly controlled A1c cohort with the properly controlled and moderately controlled A1c cohorts, we found a significant increase in amputations (p = 0.042) and cutaneous infections (p = 0.0438), respectively. When evaluating non-diabetics to diabetic patients, significantly increased rates of amputations (p < 0.0001), cutaneous infections (p = 0.0485), systemic infections (p = 0.0066), and AKF (p = 0.0005) were noted in the latter. Conclusions: Poorly controlled diabetes shows a significant correlation with increased complications following foot and ankle burns, including amputations, infections, and AKF.