ITE CA-2 Pediatric Anesthesia Flashcards
Pre-term baby resp distress with positive meconium at birth
Nasal CPAP has lowered the incidence of BPD when compared to intubation and ventilation in neonates
Nasal CPAP decreases atelectasis and maintains recruitment.
Advantages of the nasal route are that neonates are obligate nose-breathers (until 5 months of age) and a full facemask may cause facial/nasal pressure necrosis. Also, there is some evidence that nasal CPAP is superior to intubation and mechanical ventilation in preventing broncho-pulmonary dysplasia.
Neonates lung volumes
Neonates have higher closing capacity and a lower functional reserve capacity compared to adults
Functional residual capacity is lower in neonates, but this increases over the first few days of life and reaches adult levels at about day 4.
Symptomatic tachy in a kid with QRS 0.11
Wide complex tachycardia with evidence of cardiopulmonary compromise should be treated with synchronized cardioversion (0.5-1 J/kg).
Wide complex QRS is defined as greater than 0.09 seconds duration in children.
Child asymptomatic tachy wide QRS
If the patient with a wide complex tachycardia is hemodynamically stable without evidence of cardiopulmonary compromise then adenosine may be administered. The AHA also recommends consultation for possible amiodarone or procainamide administration.
Peds narrow complex tachy
Narrow complex tachycardia can be divided into probable sinus tachycardia versus probable supraventricular tachycardia (SVT). P-waves are present in sinus tachycardia and HR is typically less than 220/min for an infant and 180/min for children (150/min for adults). Supraventricular tachycardia has either absent P-waves or morphologically abnormal P-waves with fixed HR typically > 220 for infants and > 180 for children. Vagal maneuvers and/or adenosine are recommended as first line therapy for SVT. If adenosine is ineffective or IV/IO access is not available, then proceed with synchronized cardioversion. Sinus tachycardia therapy includes treating the cause.
Differences for spinal between infants and adults
Spinal anesthesia in infants has many differences compared to adults including increased speed of onset, decreased duration of action, lack of hemodynamic collapse, and increased block spread owing to anatomic differences in the spinal cord
Sign of high spinal in infant
Apnea
CSF volume and distribution
CSF volume (10 mL/kg in neonates vs 4 mL/kg in infants vs 3 mL/kg in children vs 2 mL/kg in adults) and distribution (50/50 split between brain and spinal cord and 70/30 split in adults)
Factors that contribute to closure of the ductus arteriosus include
Factors that contribute to closure of the ductus arteriosus include decrease in PVR, increase in SVR, increase in PaO2 > 50 mmHg (causes arterial smooth muscle of the ductus to contract), normocarbia, and euvolemia.
When does ductus arteriosus close? Foramen ovale?
Fetal PVR is high due to lack of oxygen in the alveoli. With the first breath of life, alveoli fill with oxygen and the infant’s PVR decreases. As PVR decreases, SVR increases and the ductus arteriosus functionally closes within the first 12-24 hrs. As a result, more blood flows through the lungs and into the left atrium. This results in functional closure of the foramen ovale. It will take several months for the ductus arteriosus and the foramen ovale to close
If the ductus arteriosus does not functionally close within __ days of birth, it is considered a PDA.
If the ductus arteriosus does not functionally close within 4 days of birth, it is considered a PDA. Premature infants with birth asphyxia and neonatal respiratory distress syndrome are the most likely patients to have complications from a PDA. The diagnosis of persistent fetal circulation or persistent pulmonary hypertension of the newborn can be made by noting a > 20 mmHg difference in PaO2 between preductal (e.g. right radial artery) and postductal (e.g. umbilical, posterior tibial, or dorsalis pedis) arterial lines
The diagnosis of persistent fetal circulation or persistent pulmonary hypertension of the newborn can be made by
If the ductus arteriosus does not functionally close within 4 days of birth, it is considered a PDA. Premature infants with birth asphyxia and neonatal respiratory distress syndrome are the most likely patients to have complications from a PDA. The diagnosis of persistent fetal circulation or persistent pulmonary hypertension of the newborn can be made by noting a > 20 mmHg difference in PaO2 between preductal (e.g. right radial artery) and postductal (e.g. umbilical, posterior tibial, or dorsalis pedis) arterial lines
Neonatal resuscitation
If a neonate’s heart rate is less than 60 bpm for greater than 30 seconds despite adequate ventilation with supplemental oxygenation, chest compressions are indicated. Chest compressions should be performed in a 3:1 ratio with ventilation at a rate of 120 events per minute (i.e. 90 chest compressions and 30 breaths total per minute), and full chest recoil should be allowed after each compression. This should continue until the neonate’s heart rate is > 60 bpm.
Pyloric stenosis acid base presentation
Pyloric stenosis commonly presents as a hypochloremic, hypokalemic, metabolic alkalosis with compensatory respiratory acidosis. Elevated serum bicarbonate is often present along with increased urine specific gravity and decreased urine chloride.
TrueLearn Insight : Metabolic alkalosis must be corrected before a pyloromyotomy in order to prevent postoperative central apnea due to CSF alkalosis. Pyloric stenosis and pyloromyotomies are therefore NOT surgical emergencies.
Nonshivering thermogenesis
what is it
what triggers it
what inhibits it
Nonshivering thermogenesis is the major source of heat production in neonates and infants. It is triggered by norepinephrine, glucocorticoids, and thyroxine. It is inhibited by inhalational anesthetics and β-blockers.
pyloric stenosis acid/base disturbance
Pyloric stenosis commonly presents as a hypochloremic, hypokalemic, metabolic alkalosis with compensatory respiratory acidosis. Elevated serum bicarbonate is often present along with increased urine specific gravity and decreased urine chloride.
TrueLearn Insight : Metabolic alkalosis must be corrected before a pyloromyotomy in order to prevent postoperative central apnea due to CSF alkalosis. Pyloric stenosis and pyloromyotomies are therefore NOT surgical emergencies.
Anesthetic management for congenital diaphragmatic hernia in a newborn
CDH should be managed using lower tidal volume ventilation with permissive hypercapnia (PaCO2 up to 65 mm Hg), maintenance of SpO2 90-95% preductally, maintenance of normothermia, and with prevention of worsening pulmonary hypertension
most common croup organism
parainfluenza
Caudal blockade dosing
Sacral 0.5 ml/kg
Lumbar 1 ml/kg
Mid thoracic 1.25 ml/kg
steeple sign
croup
barking cough
croup
treatment for croup
racemic epi
thumbprint sign
epiglottitis
fever, increased secretions, resp failure, tripod position
epiglottitis
Retinopathy of prematurity most common in most cited cause course of disease treatment
Retinopathy of prematurity is most common in infants less than 1200 grams with a most cited cause of hyperoxia. Most of those affected have spontaneous regression to normal vision; and a general anesthetic is necessary for treatment as a still surgical field is needed.
Children oxygen consumption
Children, especially infants, desaturate quickly due to increased oxygen consumption (up to 7-8 mL/kg/min).
The most common causes of postintubation croup
The most common causes of postintubation croup are subglottic injury and edema associated with traumatic intubation, an oversized endotracheal tube, or an overinflated ETT cuff. The latter is likely if no air leak exists at 30-40 cm H2O with positive airway pressure.
med to prevent postintubation croup
Dexamethasone (0.5 mg/kg IV, max 10 mg) has been shown to be effective in reducing postintubation croup.
Treatment for postintubation croup
Severity of postintubation croup can be measured by the Clinical Croup Score which can help dictate treatment. Mild postintubation croup can be treated with cool, humidified mist, while moderate-severe (7+ score) symptoms benefit from nebulized racemic epinephrine followed by 4-5 hours of monitoring to watch for rebound effects.
Ear tubes in kid with trisomy 21
Myringotomy and tube placement often involves a rapid inhaled anesthetic with avoidance of premedication, intubation, and intravenous catheter placement. Instead, intramuscular, intranasal, oral, and rectal routes for medication administration are used. However, the anesthesiologist should be prepared to alter these plans for patients with complex medical problems such as patients with Down syndrome. For patients who have inflexible cervical spines or cervical spines at risk for atlantoaxial instability, tilting of the bed should be employed, and excess movement of the neck should be avoided. Supraglottic devices may be needed, and an intravenous catheter should be considered in Down syndrome patients presenting for this procedure.
Define fetal acidemia
Scalp blood gas pH less than 7.2
Or
Lactate greater than 4.8