A5011251019- Neonatal Health and Biochemistry
- COVID-19 Clinical Research Studies
- Methemoglobinemia and Tumor Lysis Syndrome
- Urological Disorders and Treatments
- Congenital Anomalies and Fetal Surgery
- Congenital Diaphragmatic Hernia Studies
- Respiratory viral infections research
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Homelessness and Social Issues
- Cardiovascular Issues in Pregnancy
- Renal Diseases and Glomerulopathies
- Blood groups and transfusion
- Pneumonia and Respiratory Infections
- Central Venous Catheters and Hemodialysis
- Acute Myocardial Infarction Research
- Diabetes and associated disorders
- Intestinal and Peritoneal Adhesions
- Complement system in diseases
- Intestinal Malrotation and Obstruction Disorders
- Hormonal Regulation and Hypertension
- Vascular Anomalies and Treatments
- Kawasaki Disease and Coronary Complications
- Hemoglobinopathies and Related Disorders
- Appendicitis Diagnosis and Management
- SARS-CoV-2 and COVID-19 Research
University of Kansas
2020-2022
Smt. N.H.L. Municipal Medical College
2021
University of South Florida
2021
Children's Hospital Central California
2021
Wichita State University
2021
United Hospital
2021
United Hospital Center
2021
Brookdale University Hospital and Medical Center
2021
Although a growing body of evidence suggests that early transition to oral antimicrobial therapy is equally efficacious prolonged intravenous antibiotics for treatment acute pediatric osteomyelitis, little known about the trends in peripherally inserted central catheter (PICC) placements. Using national database, we examined incidence rates hospitalizations osteomyelitis United States from 2007 through 2016, as well PICC placement, length stay (LOS), and cost associated with these...
To explore trends in hospitalization rate, resource use, and outcomes of Kawasaki Disease (KD) children the United States from 2008 to 2017.This was a retrospective, serial cross-sectional analysis pediatric hospitalizations with International Classification diagnostic codes for KD National Inpatient Sample. Hospitalization rates per 100 000 populations were calculated stratified by age group, gender, race, US census region. Prevalence coronary artery aneurysms (CAA) expressed as proportions...
To evaluate the trends in hospitalization for kernicterus United States from 2006 through 2016.Repeated, cross-sectional analysis of to 2016 editions Kids' Inpatient Database. All neonatal hospitalizations with an International Classification Diseases, Ninth or Tenth Revision, Clinical Modification code and admitted at age ≤28 days were included.Among 16 094 653 2016, 20.5% diagnosed jaundice overall incidence 0.5 per 100 000. The rate (per 000) was higher among males (0.59), Asian Pacific...
Background The incidence rate and economic burden of neonatal abstinence syndrome (NAS) are increasing in the United States (US). We explored link between length stay (LOS) hospitalization cost for 2018. Methods This was a cross-sectional analysis 2018 national inpatient sample database. Newborn hospitalizations with their accompanying comorbid conditions were identified using International Classification Diseases, 10th Edition diagnostic codes. Logistic regression used to determine impact...
To evaluate the trends in hospitalization for neonatal jaundice and its management with phototherapy exchange transfusion United States from 2006 through 2016.Repeated, cross-sectional analysis of to 2016 editions Kids' Inpatient Database. All hospitalizations an International Classification Diseases, 9th or 10th Revision, Clinical Modification code admitted at age ≤28 days were included. The outcome measures changes diagnosis (expressed as a proportion) over years.Among 16 094 653 2016,...
Hemolytic Uremic Syndrome (HUS) is a constellation of microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure. Shiga toxin-producing Escherichia coli- (STEC-) mediated HUS common cause failure in children can rarely result severe neurological complications such as encephalopathy, seizures, cerebrovascular accidents, coma. Current literature supports use eculizumab, monoclonal antibody that blocks complement activation, atypical (aHUS). However, those with neurologic from...
Vasudeva, Rhythm1; Bhatt, Parth2; Lilje, Christian3; Desai, Pooja4; Amponsah, Jason5; Umscheid, Jacob6; Parmar, Narendrasinh7; Neel8; Adupa, Reshmi9; Pagad, Sukrut10; Agrawal, Prerna11; Donda, Keyur12; Dapaah-Siakwan, Fredrick13; Yagnik, Priyank14 Author Information
Abstract Background Autoimmune Polyendocrine Syndrome type 1 (APS-1) is an autosomal recessive rare disease resulting from mutations in the autoimmune regulator gene (AIRE) on chromosome 21q22.3. APS-1 was first described as a syndrome 1946 triad of mucocutaneous candidiasis, primary hypoparathyroidism, and adrenal insufficiency. With AIRE mutation, immune system will have T-regulatory cell defect, which leads to loss tolerance. This increase risk body's organs such pancreas, thyroid, gland,...