Sydney A Mashaw

Ms. Sydney A Mashaw

orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

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

Representative Publications

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1 April 2024 in Current Pain and Headache Reports
Verified
Journal Article
Closed access
PDF file
SVSage V.
Sage V.
MGMelanie A. Green
Melanie A. Green
SMSydney A Mashaw
Sydney A Mashaw
WBWilliam D. Brouillette
William D. Brouillette
ANAngela Nguyen
Angela Nguyen
Alan David KayeAlan David Kaye
Alan David Kaye

25 June 2025 in Current Pain and Headache Reports
Verified
Journal Article
Closed access
PDF file
Alan David KayeAlan David Kaye
Alan David Kaye
HCHarrison David Cooper
Harrison David Cooper
SMSydney A Mashaw
Sydney A Mashaw
AAAhmed Ibrahim Anwar
Ahmed Ibrahim Anwar
AHAlex V. Hollander
Alex V. Hollander
SSSahar Shekoohi
Sahar Shekoohi

Verified
Journal Article
Open access
PDF file
Alan David KayeAlan David Kaye
Alan David Kaye
GCGrant Coffman
Grant Coffman
SMSydney A Mashaw
Sydney A Mashaw
ATAustin Thomassen
Austin Thomassen
KBKalob M. Broocks
Kalob M. Broocks
SSSahar Shekoohi
Sahar Shekoohi
Niacin therapy has been a mainstay in traditional secondary prevention of stroke. Supplemental use of niacin has been used to improve lipid panel markers, including lowering low-density lipoproteins and triglycerides, and raising high-density lipoproteins, which have been associated with lower risk for stroke. This supplementation has been supported by earlier studies regarding niacin and its role in reducing cardiovascular risk. However, recent studies have called into question the efficacy of niacin therapy and some studies even show negative effects that are associated with taking supplemental niacin. In the present investigation, review of niacin-mediated benefits to cardiovascular disease and newer research suggesting that niacin may be ineffective with the potential of adverse side effects are summarized. This review further highlights the need for more population-level studies regarding the effects of supplemental niacin use to provide a scientific basis for its therapeutic role in cardiovascular disease, including improvement in lipid panel markers and stroke prevention.

8 January 2025 in Heliyon
Verified
Journal Article
Open access
Alan David KayeAlan David Kaye
Alan David Kaye
EVEmily A. Villafarra
Emily A. Villafarra
EEErin S. Everett
Erin S. Everett
EWErin Ware
Erin Ware
SMSydney A Mashaw
Sydney A Mashaw
SSSahar Shekoohi
Sahar Shekoohi
The objective of this study was to analyze available evidence on efficacy and safety of sugammadex in reversing neuromuscular blockades in patients with Myasthenia Gravis (MG), thereby providing a comprehensive understanding of its potential benefits and risks in this specific patient population. We performed a systematic search for studies from PubMed, Embase, Web of Science, and Google Scholar. Sources were screened using Rayyan, following predefined inclusion and exclusion criteria focusing on English articles published from 2010 to 2024 on MG patients under general anesthesia. Data on patient characteristics and outcomes were extracted, and quality was appraised using the JBI Critical Appraisal Checklist. Out of 361 initial citations, 24 studies met inclusion criteria. Sugammadex demonstrated rapid and effective reversal of neuromuscular blockades, with ToF recovery times ranging from 79.7 s to 10 min, and short extubation times. The incidence of postoperative myasthenic crisis was low, and no mortalities were reported. Sugammadex may serve as a reasonable option for the reversal of neuromuscular blockades in MG patients, indicating potential for rapid recovery and a relatively low incidence of serious complications. However, due to the limited number of studies and the nature of the evidence available, further large-scale and rigorous investigations are warranted to better establish its superiority over traditional reversal agents.

18 April 2025 in Healthcare
Verified
Journal Article
Open access
PDF file
SMSydney A Mashaw
Sydney A Mashaw
AAAhmed Ibrahim Anwar
Ahmed Ibrahim Anwar
JVJudy N. Vu
Judy N. Vu
ATAustin Thomassen
Austin Thomassen
Maya BeesleyMaya Beesley
Maya Beesley
Alan David KayeAlan David Kaye
Alan David Kaye
Background: Agitation is a frequent and challenging symptom in schizophrenia and bipolar disorder, characterized by heightened motor activity, emotional distress, and potential aggression. This symptom is most observed during acute episodes, representing a significant burden on patients, caregivers, and healthcare systems. Agitation is a leading cause of emergency department visits and psychiatric hospitalizations, necessitating prompt and effective interventions to ensure safety and mitigate its far-reaching impact. Traditional treatments, including high-potency antipsychotics and benzodiazepines, remain first-line options but are associated with significant drawbacks such as sedation, extrapyramidal symptoms, tolerance, and limited applicability in certain patient populations, especially those with respiratory or cardiac depression and the elderly. Non-pharmacologic strategies like de-escalation techniques and environmental modifications are invaluable but may be impractical in acute care settings, as speed and efficiency are critical in emergent settings. These limitations, including the onset of extrapyramidal symptoms with high-dose antipsychotics and the development of tolerance with benzodiazepines, highlight gaps in care, including the need for faster-acting, safer, and more patient-friendly alternatives that reduce reliance on physical restraints and invasive interventions. Methods: This review explores the evolution of treatments for agitation, focusing on alternative and innovative approaches. To highlight these treatments, an extensive review of the literature was conducted utilizing PubMed, Google Scholar, Embase.com, and other search engines. Results: Key developments include sublingual dexmedetomidine, recently FDA-approved, which offers sedation without respiratory depression and a non-invasive administration route. Similarly, subcutaneous olanzapine provides a more convenient alternative to intramuscular injections, reducing injection-related complications. Other emerging treatments such as gabapentin, pregabalin, and ketamine show promise in addressing agitation in specific contexts, including comorbid conditions and treatment-resistant cases. A comparative analysis of these therapies highlights their mechanisms of action, clinical evidence, and practical challenges. Conclusions: Future directions emphasize intranasal delivery systems, novel pharmacologic agents, and potential roles for cannabinoids in managing agitation. These innovations aim to balance rapid symptom control with improved patient safety and experience. The set back with these emerging techniques is a lack of standardized dosing and protocols. They also face ethical concerns, including the chance of misuse or abuse, as well as regulatory barriers, as they lack FDA approval and their legality changes between states. This review underscores the clinical, practical, and ethical considerations in advancing care for agitated patients, paving the way for more effective and compassionate management strategies in psychiatric settings.