Erin Ware

Ms. Erin Ware


Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

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

Representative Publications

View All Publications
24 March 2025 in Current Pain and Headache Reports
Verified
Journal Article
Closed access
PDF file
GEGabrielle K. Eaves
Gabrielle K. Eaves
EWErin Ware
Erin Ware
DTDevin R. Touchet
Devin R. Touchet
WHWhitney K. Hamilton
Whitney K. Hamilton
SNSteele S. Netterville
Steele S. Netterville
Alan David KayeAlan David Kaye
Alan David Kaye

8 May 2025 in Children
Verified
Journal Article
Open access
PDF file
ACAmber Cradeur
Amber Cradeur
AJAaron Jackson
Aaron Jackson
EWErin Ware
Erin Ware
TFTorrey Louise Fourrier
Torrey Louise Fourrier
GMGauri Mankekar
Gauri Mankekar
Background/Objectives: Congenital cytomegalovirus (cCMV) infection is a significant cause of pediatric hearing loss. However, the prevalence and characteristics of cCMV-related hearing loss remain unclear. Methods: A comprehensive search of major databases (PubMed, Scopus, and Web of Science) was conducted to identify studies and reviews published between 2000 and 2024 that investigated cCMV infection, testing for cCMV, and pediatric hearing loss. Studies were included if they reported on the prevalence, characteristics, current policies, and recommendations for universal cCMV testing in newborns. Results: This review highlights key issues: cCMV is a significant and treatable cause of pediatric hearing loss; most cCMV-related hearing loss cases presented with bilateral and profound hearing impairment; and cCMV testing is performed only for babies who fail newborn hearing screening. Conclusions: This narrative review highlights the significant association between cCMV infection and pediatric hearing loss. Currently, targeted cCMV testing is recommended for newborns who fail newborn hearing screening. Universal cCMV testing may facilitate early diagnosis and directed intervention and could be cost-effective in the long run.

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.