15 results
algorithm fever management febrile antibiotics lp risk stratification ultrasound fracture skull 21hydroxylasedeficiency 21ohd abuse assessment bruising creactiveprotein crp differential disease
Validation of the Step-By-Step Approach to Febrile Infants #Diagnosis #Management #Pediatrics #Peds #Febrile #Infant #StepByStep #Algorithm #LP
Approach to Febrile Infants ... #Diagnosis #Management ... #Pediatrics #Peds ... #Febrile #Infant ... #StepByStep #Algorithm
Step by Step Algorithmic Approach to Pediatric Fever Age < 21 days old (or 28 days for
Algorithmic Approach to Pediatric ... ANC > 10000 #Pediatrics ... #Peds #Diagnosis ... #Management #StepByStep ... #Algorithm #Infant
“Step by Step” – the new kid on the block – aims to risk stratify this
“low risk” an infant ... CRP < 20 mg/L #Diagnosis ... #Management #Pediatrics ... #Peds #Febrile ... #Infant #StepByStep
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children Urinary
Clinical Algorithm ... do not replace clinical ... UTI #Algorithm #Diagnosis ... #Peds #UrinaryTract ... #Pediatrics #Fever
Standardized Physical Abuse Guideline <6 months of age • Social work consult • Skeletal survey • Head
age • Social work ... • Troponin for infants ... Abuse #Guidelines #Workup ... #Peds #Pediatrics ... #Diagnosis
Pediatric Skull Fracture with Associated Hematoma on POCUS Working with the challenges of risk stratification, management of
Pediatric Skull ... management of peds ... Making PECARN work ... #Peds #Pediatrics ... #Clinical #Ultrasound
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 The Febrile Infant Step-by-Step Algorithm This is an algorithm developed by European emergency physicians to identify low-risk
The Febrile Infant ... 92.0% and 46.9% #Diagnosis ... EBM #Management #Pediatrics ... #Peds #Febrile ... #Infant #StepByStep
The infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... Other causes #Diagnosis ... #Peds #Pediatrics ... #Infant #Tachypnea
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Hirsutism & acne • Infertility ... endocrinology #peds ... #pediatrics
Figure 53 – Longitudinal (left) and transverse (right) images from an ultrasound of the pylorus demonstrate
criteria for the diagnosis ... #Clinical #POCUS ... #Peds #Pediatrics
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