Ped/OB Exam Review Flashcards
Arnold-Chiari malformation may have what symptoms?
Recurrent Aspiration
Syndactyly, Cloverleaf Skull, Hypertolerism, and Midface Hyperplasia are characteristics of what syndrome?
Apert Syndrome
What induction drug should be avoided in Arnold-Chiari malformation surgery?
Ketamine (↑ ICP concerns)
Which Chiari malformation is most often associated with spinal bifida?
Type II (Arnold-Chiari)
Most common pediatric craniofacial defect
Cleft Palate
Anesthesia Intervention for Cleft Palate
- Video Laryngoscopy
- Dexemetomidine Infusion
Congenital Diaphragmatic Hernia is a defect that involves _________.
Hypoplastic Lung Tissue
What is the condition?
Gastroschisis
Indications for Craniofacial Surgery
- Psychosocial Reasons
- Severe Exopthalmus
Down Syndrome Anesthesia Induction Considerations
- Post extubation stridor
- Bradycardia
- Potential Airway Obstruction
Intervention for the Following ETCO2
- Increase FiO2 to 100%
- Ask the surgeon to stop stimulating the patient
Anesthesia Considerations for Encephalocele
Challenging airway for the anesthesia provider.
Goldenhar Syndrome Characteristic
- Cleft Palate
- Mandibular Hypoplasia
Gastroschisis and Omphalocele surgical concerns for Anesthesia.
- Monitoring signs of impeded venous return
- Hypothermia
- Hypovolemia
What is the congenital syndrome?
Meningocele
Anesthesia concern for bilateral microtia
Difficult airway
What is this causing?
Hypertrophied Pylorus Muscle
What does Pyloric Stenosis cause?
OUTLET obstruction
Crouzon Syndrome features
- Midface hypoplasia
- Proptosis
Inspiratory stridor and retraction at the suprasternal notch are symptoms associated with what?
Laryngospasm
If ETT luminal diameter decreases by 2 mm in a pediatric patient, what would be the increase in airway resistance?
32x increase in airway resistance
What is the syndrome?
Pierre Robin Syndrome
This syndrome requires a tongue suture to prevent glossoptosis in PACU.
Pierre Robin Syndrome
What acid-base balance is seen with Pyloric Stenosis?
Hypokalemic/ Hypochloremic Metabolic Alkalosis
Long-term complications seen from untreated Scoliosis
- Decrease lung compliance
- Recurrent Lung infections
What type of scoliosis is associated with cardiac and urological abnormalities along with hemifacial microsomia
Congenital Scoliosis
Spinal Bifida is a result of what?
Failure of fusion at the vertebral arches
Which Tracheoesophageal Fistula is the most common?
Type C (blind esophageal pouch and TE Fistula coming from the trachea)
The most common location for a Congenital Diaphragmatic Hernia
Left Posterior Lateral
The primary characteristic of Down Syndrome
- Mandibular hypoplasia
- Hypotonia
- Subglottic Stenosis
Primary goal of managing pediatric airway with TE Fistula
Prevent aspiration pneumonitis
Three main characteristics involved with the Pierre Robin triad?
- Glossoptosis
- Micrognathia
- Respiratory Distress
A higher dose of TXA would be considered for this surgical procedure
Neuromuscular Scoliosis Repair
The 3 C’s of TE Fistula
- Coughing
- Choking
- Cyanosis
Anesthesia intervention for intraoperative bronchospasm
- 100% FiO2
- Deepening Anesthetic
Anesthesia consideration for myelomeningocele
- Preservation of function
- Avoidance of further injury
- Proper position for intubation
Signs of Bronchospasm
- Expiratory Polyphonic Wheezing
- Slow upslope on the capnography monitor
Omphaloceles are associated with these anomalies
- Congenital Heart Defects
- Urologic Defects
_________ syndrome becomes more difficult to manage with age
_________ syndrome becomes easier to manage with age
- Treacher Collins is more difficult with age
- Pierre Robin is easier with age
Congenital Diaphragmatic Hernia Interventions
Small frequent tidal volumes