12 results
Newborn Assessment - APGAR Score

Assessment of newborn vital signs following labor via a 10-point scale evaluated
Newborn Assessment ... Assessment of newborn ... develop long-term neurologic ... #Diagnosis #Peds ... #Pediatrics #APGAR
Neonatal Infant Pain Scale (NIPS)

For infants less than one year of age, the Neonatal Infant Pain
A score of 0-2 indicates ... A score of 5 or ... #Diagnosis #Peds ... #Pediatrics #PainScale ... #NIPS #Assessment
Asymmetrical Tonic Neck Reflex (ATNR)

This primitive reflex found in newborn babies that normally vanishes around 4
known as the "fencing ... position of the infant's ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... #Diagnosis #Peds ... #Pediatrics #Infant ... #Differential #Assessment
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
relatively common finding ... The skin in this infant ... This finding resolved ... #clinical #photo ... #peds #pediatrics
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
this video, the infant ... Sign #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds #neurology
The asphyxia escape reflex is assessed by placing the child in the prone position on the
with the face facing ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
To be eligible for hospice beneficiaries with Alzheimer’s disease must have a FAST Scale of greater
Sub-stage 7a: Ability ... #FAST #Stage #Score ... #Alzheimers #Dementia ... #Functional #Assessment ... Hospice #Diagnosis #Geriatrics
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... if they have no clinical ... effusion, or z scores ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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 ... • Early: decr feeding ... endocrinology #peds ... #pediatrics