Publications by authors named "Ashton Ingold"

Article Synopsis
  • NPIs significantly reduced asthma exacerbations and viral infections in pediatric patients during their enforcement from March 2020 to December 2022.
  • A total of 5,758 asthma exacerbations were recorded, with a 50% decline during NPIs, while 87% of the 70,682 respiratory tests returned positive for pathogens but showed decreased rates for some viruses.
  • After the NPIs ended, asthma exacerbations returned to pre-pandemic levels, and an unexpected spike in respiratory syncytial virus infections highlighted the importance of ongoing monitoring.
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Purpose: To identify characteristics of SARS-CoV-2 infection that are associated with hospitalization in children initially evaluated in a Pediatric Emergency Department (ED).

Methods: We identified cases of SARS-CoV-2 positive patients seen in the Arkansas Children's Hospital (ACH) ED or hospitalized between May 27, 2020, and April 28, 2022, using ICD-10 codes within the Pediatric Hospital Information System (PHIS) Database. We compared infection waves for differences in patient characteristics and used logistic regressions to examine which features led to a higher chance of hospitalization.

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Unlabelled: Non-pharmacologic interventions (NPIs), such as universal masking, implemented during the SARS-CoV-2 pandemic have reduced respiratory infections among children. This study evaluated the impact of NPIs on infections in children, analyzing data from two hospitals in Arkansas and examining age-related differences and co-infections with other respiratory viruses. The study was approved by the Institutional Review Board and included patients (≤18 years) with upper respiratory tract symptoms.

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Article Synopsis
  • Whole Genome Sequencing (WGS) of SARS-CoV-2 is essential for tracking COVID-19, with various primer schemes like Midnight and ARTIC V4.1 used for amplification, although they face challenges like amplicon dropouts due to mutations.
  • This study employs seven long-range PCR primer pairs to sequence SARS-CoV-2, producing larger amplicons (about 4500 bp) that cover the entire genome, including the important S-gene, and compares their effectiveness to traditional primers.
  • Results indicate that using long-range primers significantly minimizes coverage bias and amplicon dropout, thereby improving the accuracy of identifying SARS-CoV-2 variants, crucial for monitoring emerging strains.
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Introduction: Non-pharmacologic interventions (NPIs), such as universal masking, implemented during the SARS-CoV-2 pandemic have reduced respiratory infections among children. This study focuses on evaluating the impact of NPIs on infections in children, analyzing data from two hospitals in Arkansas, and examining age-related differences and coinfections with other viruses.

Methods: The study was approved by the Institutional Review Board and included patients aged ≤18 years with upper respiratory tract symptoms.

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Whole Genome Sequencing (WGS) of the SARS-CoV-2 virus is crucial in the surveillance of the COVID-19 pandemic. Several primer schemes have been developed to sequence the ~30,000 nucleotide SARS-CoV-2 genome that use a multiplex PCR approach to amplify cDNA copies of the viral genomic RNA. Midnight primers and ARTIC V4.

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Purpose: To identify characteristics of SARS-CoV-2 infection that are associated with hospitalization in children initially evaluated in a Pediatric Emergency Department (ED).

Methods: We identified cases of SARS-CoV-2 positive patients seen in the Arkansas Children's Hospital (ACH) ED or hospitalized between May 27, 2020, and April 28, 2022 using ICD-10 codes within the Pediatric Hospital Information System (PHIS) Database. We compared infection waves for differences in patient characteristics, and used logistic regressions to examine which characteristics led to a higher chance of hospitalization.

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An eleven-year-old tested positive for SARS-CoV-2 Lambda variant. Sequencing was performed on the Oxford Nanopore and the Illumina NextSeq 500. Both platforms identified all 7 of the synonymous mutations in the sample, while all 28 nonsynonymous mutations were identified from Oxford Nanopore and 20 nonsynonymous mutations were identified from Illumina.

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