Publications by authors named "Jeong Yong Lee"

Background: To develop and validate machine learning (ML)-based models to predict serious bacterial infections (SBIs) in febrile infants aged ≤90 days.

Methods: This retrospective study analysed data from febrile infants (≥38.0℃) aged ≤90 days.

View Article and Find Full Text PDF

Background: The decision to perform immediate brain magnetic resonance imaging (MRI) in children with their first unprovoked seizure presenting to the emergency department (ED) remains a clinical challenge. We aimed to identify clinical factors associated with the detection of epileptogenic lesions and emergent neuroimaging findings on MRI to determine the imaging necessity and urgency, respectively.

Methods: We retrospectively enrolled pediatric patients (age 0-18 years) presenting to a single institution's pediatric ED with new-onset unprovoked seizures between January 2010 and December 2023.

View Article and Find Full Text PDF

Background: Diagnosing acute appendicitis in children is often difficult due to non-specific symptoms and limited cooperation during physical examination. This study aimed to evaluate the diagnostic utility of the Jumping-Up (J-Up) test, and to compare it with traditional physical signs.

Methods: We conducted a prospective observational study from September 2021 to July 2023 in the pediatric emergency department of Asan Medical Center Children's Hospital in Seoul, Korea.

View Article and Find Full Text PDF

This study compared the emergency department (ED) flow of young infants under 90 days old presenting with gastrointestinal symptoms who underwent point-of-care ultrasound (POCUS) versus X-ray (XR) as their primary imaging test. The study retrospectively enrolled infants under 90 days old with gastrointestinal (GI) symptoms who visited a tertiary university-affiliated hospital ED from January 2019 to September 2022. The patients were divided into 2 groups based on whether they received XR or POCUS as their first imaging test.

View Article and Find Full Text PDF

Objectives: This study aimed to develop machine learning (ML) prediction models for identifying bloodstream infection (BSI) and septic shock (SS) in pediatric patients with cancer who presenting febrile neutropenia (FN) at emergency department (ED) visit.

Materials And Methods: A retrospective study was conducted on patients, younger than 18 years of age, who visited a tertiary university-affiliated hospital ED due to FN between January 2004 and August 2022. ML models, based on XGBoost, were developed for BSI and SS prediction.

View Article and Find Full Text PDF

Background: Recent reports have demonstrated promising results regarding the use of ketamine sedation for reducing pediatric intussusception without an associated elevated risk of bowel perforation. However, data on direct intraluminal pressure are still lacking. This study aimed to investigate sedation safety, primarily by comparing intraluminal pressure.

View Article and Find Full Text PDF
Article Synopsis
  • Primary ovarian insufficiency (POI) is a condition causing menstrual disturbances and ovarian dysfunction in women before age 40, with a prevalence of less than 1% that may vary based on ethnicity.
  • The study investigated specific genetic polymorphisms in the follicle-stimulating hormone receptor (FSHR), estrogen receptor 1 (ESR1), and their relation to ovarian health in 139 Korean patients with POI compared to 350 controls.
  • Significant associations were found between certain genotype combinations and the risk of POI, particularly involving FSHR and ESR1, which could point to genetic factors influencing the condition's prevalence and enhance understanding for potential treatments.
View Article and Find Full Text PDF
Article Synopsis
  • Primary ovarian insufficiency (POI) is a major cause of female infertility occurring before age 40, associated with TGF-β/BMP signaling pathway genes like TGF-β and BMP15.
  • The study aimed to explore the link between specific gene polymorphisms in this pathway and the risk of developing POI, examining data from 139 patients with POI and 345 controls.
  • Results indicated that certain allele combinations in TGFBR1 and TGFBR3 genes were linked to a reduced risk of POI, suggesting these polymorphisms could serve as potential biomarkers for diagnosing and treating the condition.
View Article and Find Full Text PDF

Idiopathic recurrent pregnancy loss (RPL) is defined as at least two pregnancy losses before 20 weeks of gestation. Approximately 5% of pregnant couples experience idiopathic RPL, which is a heterogeneous disease with various causes including hormonal, chromosomal, and intrauterine abnormalities. Although how pregnancy loss occurs is still unknown, numerous biological factors are associated with the incidence of pregnancy loss, including genetic variants.

View Article and Find Full Text PDF
Article Synopsis
  • * STAT3 is essential for successful embryo implantation, and while its connection to RIF is known, the effect of specific genetic variations in miRNAs on STAT3's role in RIF has not been fully explored.
  • * A study involving 161 RIF patients and 268 healthy individuals found that the genetic variant miR-34a rs6577555 C>A is significantly associated with increased RIF risk, indicating it may play a role in the condition, warranting further research.
View Article and Find Full Text PDF

This scoping review analyzed statements from 22 medical organizations in the United States to identify commonalities in the definition and governance of point-of-care ultrasound (POCUS). A total of 41 statements were included. The review found that the most commonly used elements in defining POCUS were "focused," "bedside," and "patient care.

View Article and Find Full Text PDF

As populations around the world age, interest in healthy aging is growing. One of the first physical changes that occurs with aging is the loss of muscle mass and strength, termed sarcopenia. Sarcopenia limits the activity of older people, reduces their quality of life, and increases the likelihood of their developing disease.

View Article and Find Full Text PDF

Coronary artery disease (CAD) is a prevalent cardiovascular condition characterized by the accumulation of plaque within coronary arteries. While distinct features of CAD have been reported, the association between genetic factors and CAD in terms of biomarkers was insufficient. This study aimed to investigate the connection between genetic factors and CAD, focusing on the thymidylate synthase () gene, a gene involved in DNA synthesis and one-carbon metabolism.

View Article and Find Full Text PDF
Article Synopsis
  • * The study examined 151 RIF patients and 321 healthy individuals in Korea to find genetic polymorphisms associated with RIF prevalence, focusing on certain genes related to inflammation.
  • * Significant associations were found between specific polymorphisms (rs1053004, rs1800796, and rs1800629) and the likelihood of experiencing RIF, marking the first investigation of its kind in Korea.
View Article and Find Full Text PDF

Objectives: Testicular torsion (TT) is a pediatric surgical emergency that requires prompt treatment. This study investigated the feasibility of point-of-care ultrasound (POCUS) for diagnosing TT in the pediatric emergency department (ED).

Methods: We retrospectively reviewed the medical records of patients, aged 18 years or younger, who visited a university-affiliated hospital pediatric ED with acute scrotal pain without trauma history and underwent diagnostic ultrasounds between January 2010 and October 2022.

View Article and Find Full Text PDF
Article Synopsis
  • * A study involving 420 controls and 464 CRC patients found that the MUC4 rs1104760 A>G polymorphism may protect against CRC, while the rs2688513 A>G polymorphism is linked to higher mortality rates in CRC patients.
  • * The research highlights MUC4 rs1104760 as a potential biomarker for CRC, especially in patients with low-density lipoprotein cholesterol (LDL-C) levels, indicating a relationship between genetic factors and CRC prevention.
View Article and Find Full Text PDF

Pediatric patients undergoing diagnostic tests in the pediatric emergency room are frequently sedated. Although efforts are made to prevent adverse events, no sedation protocol has specified the optimal regimen, dosage, and interval of medication to prevent adverse events. This study analyzed the safety and efficacy of sequential pediatric sedation protocols for pediatric patients undergoing diagnostic tests in the pediatric emergency room of a single tertiary medical center.

View Article and Find Full Text PDF

Stroke is the second leading cause of death in the world. Approximately 80% of strokes are ischemic in origin. Many risk factors have been linked to stroke, including an increased level of plasminogen activator inhibitor-1 (PAI-1).

View Article and Find Full Text PDF
Article Synopsis
  • - Recurrent pregnancy loss (RPL) affects 1-5% of women and can significantly impact their reproductive health and mental well-being.
  • - The study analyzed the impact of specific genetic polymorphisms (rs4759314 A>G, rs920778 T>C, rs1899663 G>T, rs7958904 G>C) on RPL in a sample of 403 women with RPL compared to 383 healthy women.
  • - Results indicated that the rs4759314 A>G and rs920778 T>C polymorphisms were strongly linked to a higher risk of RPL, with specific haplotypes maintaining this association among Korean women.
View Article and Find Full Text PDF

Purpose: Rapid sequence intubation (RSI) using sedatives and neuromuscular blocking agents (NMBAs) is recommended for pediatric emergency endotracheal intubation (ETI), but is not frequently performed in Korea. This study aimed to verify factors associated with the underuse of RSI medications.

Materials And Methods: This multicenter retrospective study reviewed patients aged under 18 years who underwent an ETI within 24 hours of arrival at the emergency department between 2016 and 2019.

View Article and Find Full Text PDF
Article Synopsis
  • * The study focused on genetic variations in SMAD5, FN3KRP, and RUNX-1 among 388 women with RPL and 280 healthy controls, utilizing advanced genetic testing methods.
  • * Results indicated that the FN3KRP rs1046875 G>A variation significantly lowers the risk of RPL among Korean women, suggesting a potential link between FN3KRP and pregnancy complications that warrants further research.
View Article and Find Full Text PDF

(1) Background: First-pass success (FPS) of endotracheal intubation is more challenging in children than in adults. We aimed to identify factors associated with FPS of intubation in acute care settings. (2) Methods: We analyzed data of children aged <10 years who underwent intubation within ≤24 h of arrival at four Korean emergency departments (2016−2019).

View Article and Find Full Text PDF

Recurrent pregnancy loss (RPL) is the loss of two or more consecutive pregnancies before 20 weeks of gestational age. Our study investigated whether mucin 4 (MUC4) polymorphisms are associated with RPL. MUC polymorphisms (rs882605 C>A, rs1104760 A>G, rs2688513 A>G, rs2258447 C>T, and rs2291652 A>G) were genotyped in 374 women with RPL and 239 controls of Korean ethnicity using polymerase chain reaction-restriction fragment length polymorphism analysis and the TaqMan probe SNP genotyping assay.

View Article and Find Full Text PDF

Coronary artery disease (CAD), a leading cause of death worldwide, has a complex etiology comprising both traditional risk factors (type 2 diabetes, dyslipidemia, arterial hypertension, and cigarette smoking) and genetic factors. Vascular endothelial growth factor (VEGF) notably contributes to angiogenesis and endothelial homeostasis. However, little is known about the relationship between CAD and VEGF polymorphisms in Koreans.

View Article and Find Full Text PDF