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http://dx.doi.org/10.1258/acb.2011.011085 | DOI Listing |
Clin Chem Lab Med
October 2024
Clinical Biochemistry Unit, Alfred Pathology Service, Melbourne, VIC, Australia.
Indian Pediatr
May 2024
Department of Pediatric Neurology, Kerala Institute of Medical Sciences, Trivandrum, Kerala, India.
Objective: To describe the utility of film array meningoencephalitis (FAME) panel in the management of children with acute encephalitis syndrome (AES).
Methods: A retrospective audit was conducted between January 2017 to July 2022. We included children aged < 18 years with a diagnosis of AES for whom a CSF analysis study including FAME panel testing performed within 48 hours of admission was available.
Neurol Sci
July 2024
Department of Neurosurgery, Zhangzhou Affiliated Hospital of Fujian Medical University, Xiamen University, Zhangzhou, 363300, Fujian, China.
Background: Shunt obstruction is a type of ventriculoperitoneal shunt (VPS) failure. Whether changes in cerebrospinal fluid (CSF) parameters can influence shunt outcomes or not is debatable.
Methods: In this study, we retrospectively included adult hydrocephalus patients who received VPS from 6 general hospitals in different provinces of China from November 2013 to September 2021.
Curr Med Res Opin
March 2024
Department of Clinical Pharmacy and Biopharmaceutics, Faculty of Pharmacy, University of Jordan, Amman, Jordan.
Objective: This study aims to audit the adherence of Jordanian medical care staff to the guidelines provided by the Infectious Disease Society of America (IDSA) for managing pediatric patients admitted with suspected cases of meningitis.
Methods: A retrospective observational study was conducted at Jordan University Hospital (JUH). All pediatric patients admitted to JUH with suspected meningitis between January 1, 2019, and September 30, 2022, who underwent Cerebrospinal Fluid (CSF) and blood culture tests were recruited in this study unless there was a reason for exclusion.
Pediatr Infect Dis J
October 2023
From the Infectious Diseases Unit, Department of General Medicine, Royal Children's Hospital, Parkville, Victoria, Australia.
Background: In settings with universal conjugate pneumococcal vaccination, invasive pneumococcal disease (IPD) can be a marker of an underlying inborn error of immunity. The aim of this study was to determine the prevalence and characterize the types of immunodeficiencies in children presenting with IPD.
Methods: Multicenter prospective audit following the introduction of routinely recommended immunological screening in children presenting with IPD.
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