- COVID-19 Clinical Research Studies
- Long-Term Effects of COVID-19
- Chromosomal and Genetic Variations
- Neonatal Health and Biochemistry
- Kawasaki Disease and Coronary Complications
- Clinical Nutrition and Gastroenterology
- Clinical Reasoning and Diagnostic Skills
- Child Nutrition and Water Access
- Neonatal Respiratory Health Research
- Machine Learning in Healthcare
- COVID-19 Impact on Reproduction
- Non-Invasive Vital Sign Monitoring
- Genomic variations and chromosomal abnormalities
- Nutrition and Health in Aging
- COVID-19 and healthcare impacts
- Emergency and Acute Care Studies
- Infectious Encephalopathies and Encephalitis
- Genomics and Rare Diseases
- Sepsis Diagnosis and Treatment
- Respiratory Support and Mechanisms
- COVID-19 diagnosis using AI
Rady Children's Hospital-San Diego
2025
University of California, San Diego
2025
Children's Hospital of Orange County
2021-2023
Walt Disney (United States)
2023
Florida Department of Health in Orange County
2022
Brown University
2015
The COVID-19 pandemic is a public health crisis that has the potential to exacerbate worldwide malnutrition. This study examines whether patients with history of malnutrition are predisposed severe COVID-19. To do so, data on 103,099 inpatient encounters from 56 hospitals in United States between March 2020 and June were retrieved Cerner Dataset. Patients 2015 2019 identified, random intercept logistic regression models for pediatric adult built controlling patient demographics,...
Data on coronavirus disease 2019 (COVID-19) infections in neonates are limited. We aimed to identify and describe the incidence, presentation, clinical outcomes of neonatal COVID-19.Over 1 million encounters at 109 United States health systems, from March 2020 February 2021, were extracted Cerner Real World Database. COVID-19 diagnosis was assessed using severe acute respiratory syndrome 2 (SARS-CoV-2) laboratory tests codes. Incidence per 100 000 estimated.COVID-19 diagnosed 918 (0.1%)...
Background/Objective: Millions of children were infected with SARS-CoV-2, and a small proportion progressed to severe disease, especially those underlying risk factors. Adult COVID-19 studies showed mortality benefits Remdesivir. Data on Remdesivir use in pediatrics are limited. We report the safety tolerability pediatric patients seen at our institution. Methods: This was retrospective cohort study <19 years old acute SARS-CoV-2 infection who received least one dose Patients followed...
<h3>Importance</h3> Identifying the associations between severe COVID-19 and individual cardiovascular conditions in pediatric patients may inform treatment. <h3>Objective</h3> To assess association previous or preexisting severity of patients. <h3>Design, Setting, Participants</h3> This retrospective cohort study used data from a large, multicenter, electronic health records database US. The included aged 2 months to 17 years with laboratory-confirmed diagnosis code indicating infection...
Cardiovascular and other circulatory system diseases have been implicated in the severity of COVID-19 adults. This study provides a super learner ensemble models for predicting among these patients.The Dataset Cerner Real-World Data was used this study. on adult patients (18 years or older) with cardiovascular between 2017 2019 were retrieved total 13 conditions identified. Among patients, 33,042 admitted positive diagnoses March 2020 June (from 59 hospitals) identified selected A 14...
Abstract This study was designed to develop and validate an early warning system for sepsis based on a predictive model of critical decompensation. Data from the electronic medical records 537,837 visits pediatric Emergency Department (ED) March 2013 December 2019 were collected. A multiclass stochastic gradient boosting built identify signs associated with death, severe sepsis, non-severe bacteremia. Model features included triage vital signs, previous diagnoses, medications, healthcare...
Array comparative genomic hybridization (aCGH) testing can diagnose chromosomal microdeletions and duplications too small to be detected by conventional cytogenetic techniques. We need consider which patients are more likely receive a diagnosis