Results 81 to 90 of about 2,477,884 (224)

Analysis of various factors Including Surgical Apgar Score affecting outcome in Trauma Patients undergoing Emergency Laparatomy [PDF]

open access: yes, 2015
AIM OF THE STUDY: 1. To correlate the Surgical Apgar score with the patient’s outcome in the form of complications (morbidity) including death within 30 days of surgery (30 day mortality). 2.
Prem Anand, A
core  

Apgar Family Reuinion

open access: yes, 2011
The Palatine family immigrated to North America in 1740 from the Palatine through Port Philadelphia, colony of Pennsylvania.

core   +1 more source

Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a de novo Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
Distal 1q43q44 deletions lead to a consistent neurodevelopmental phenotype characterized by microcephaly, corpus callosum abnormalities, and developmental delay. Despite differences in genomic architecture, overlapping deletions affecting dosage‐sensitive genes such as AKT3, HNRNPU, and ZBTB18 define the core phenotype.
Ma. Guadalupe Domínguez‐Quezada   +6 more
wiley   +1 more source

A double-blind randomized control trial to compare the effect of varying doses of intrathecal fentanyl on clinical efficacy and side effects in parturients undergoing cesarean section

open access: yesJournal of Anaesthesiology Clinical Pharmacology, 2018
Background and Aims: It is a common practice to add intrathecal lipophilic opioids to local anesthetics to improve the quality of subarachnoid block.
Muhammad Asghar Ali   +3 more
doaj   +1 more source

The Predictive Accuracy of Prenatal Ultrasound for Macrosomia—A Retrospective Cohort Study

open access: yesJournal of Clinical Ultrasound, EarlyView.
Third‐trimester fetal weight estimation has limited predictive accuracy for neonatal macrosomia (low sensitivity and PPV) but may influence clinical decisions as it is strongly associated with labor induction. Prenatal macrosomia diagnosis should therefore be cautiously interpreted. ABSTRACT Objectives This study aimed to evaluate the accuracy of third‐
Isabella Abati   +6 more
wiley   +1 more source

Neonatal assessment in the delivery room – Trial to Evaluate a Specified Type of Apgar (TEST-Apgar) [PDF]

open access: yes, 2015
Background: Since an objective description is essential to determine infant’s postnatal condition and efficacy of interventions, two scores were suggested in the past but weren’t tested yet: The Specified-Apgar uses the 5 items of the conventional Apgar ...
Gloria Valencia   +54 more
core   +2 more sources

Early enteral nutrition and neurodevelopment in very low birth weight preterm infants

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objective Very low birth weight (VLBW) preterm infants are at increased risk of neurodevelopmental impairment. Although human milk may promote brain development, the association between type of feeding at discharge and neurodevelopmental outcomes remains uncertain.
Serafina Perrone   +7 more
wiley   +1 more source

Outcome Prediction of Patients Undergoing Laparotomy using Surgical Apgar Score

open access: yesJournal of the Dow University of Health Sciences
Objective: To evaluate the predictive accuracy of the Surgical Apgar Score (SAS) in determining 30-day postoperative morbidity and mortality among adult patients undergoing laparotomy in a tertiary care setting in Karachi, Pakistan.
Cemoon Effendi   +5 more
doaj   +2 more sources

Machine Learning‐Based Risk Stratification Tool for Hearing Loss in High‐Risk Neonates

open access: yesThe Laryngoscope, EarlyView.
Machine learning models, particularly XGBoost, provide robust risk stratification for neonatal hearing loss by capturing complex interactions among clinical risk factors such as NICU stay duration and family history. To translate these predictive capabilities into routine practice, an open‐access web‐based clinical decision support tool was developed ...
Sevgi Kutlu   +4 more
wiley   +1 more source

Prenatal Exome Sequencing Identifies Dual Maternal‐Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Prenatal exome sequencing (ES) can establish rare genetic diagnoses in a fetus but may also lead to occult genetic diagnosis in a biological parent. We present a case of dual fetal and maternal diagnosis by prenatal ES, in a fetus with unexplained anemia and in a pregnant patient with sickle cell disease (SCD) and recurrent unexplained hypoxia.
Matthew A. Shear   +6 more
wiley   +1 more source

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