Peds Flashcards
Cobb angle
@ scoliosis
>10 = abnormal
>40-50 = surgery
>60-65 = pulmonary dyd
>70 = pHTN at exercise
> 110 = pHTn at rest
Duchenne concerns
airway:
- impaired larngeal reflexes
- delayed gastric emptying
- macroglossia
- scoliosis
- decreased pulm reserve
cardiac:
- cardiomyopathies
- cor pulmonale
- arryhtmias
pulm:
- scoliosis
- aspriation
- weak cough - PNA
- decreased pulm rserve
Airway duchennes
aspiration precautions
consider SV with ketamine
NO VOLATILE
NO SUX
sensitive to NMB
cardiac status in respiratory papillomatosis
RVH and core pulmonale
induce laryngeal papillomatosis
avoid sux @ child
difficult airway equipment
bronchodilator
preoxygenate
IM ketamine
IV
deep enough level to avoid bronchospasm
DL and tube
URTI
severe symptoms (fever, productive cough, malaise, pulmonary invovlement) > delay 4-6 weeks
mild symptoms (nonproductive cough, mild nasal congestion, sneeze) w/ RF and ETT required > delay 2-4 weeks
mild symptoms and no ETT required to do case safely > proceed
disorders linked to MH
central core disease
King Denborough Syndrome
side effects of dantrolene aka why no ppx
n/v
pain at injection site
oculocardiac reflex at strabismus
@ manipulatino fo eye and orbital strcutures
bradycardia
TX:
deepen anesthesia, fix hypercarbia and hypoxia, ask surgeon to stop, atropine, ask for lidocaine in rectus muscles
monitors congenital diaphragmatic hernia
pre and post ductal sat
umbilical central line (avoid neck for possible ECMO)
ASA
aline
CHD induction and airway
maintain SV, PPV may worsen
avoid worsening R to L shunting - avoid drops inSVR and increases in PVR
inhalational induction
CHD intraop complications to anticipate
hypoxia
pHTN and RHF
PTX of healthy lung with reinflation of hypoplastic lung
hypotension with closure of thorax from abd organ compression of IVC
pathophysiology of CHD
deficient b/l major airway and vessel branching not explained by compression of lungs
lung and vascular hypoplasia
lower number of alveoli - low compliance and decreased SA for air exchange, imparied oxygenation
congenital anomalies with CHD
28% CNS - spina bifida, hydrcephalus
31-23% cardiac - ASD, VSD, CoAo, ToF
20% git/malrotation, atresia
15% GUT hypospadias
transport to OR in epiglottitis
parents, anesthesiologist, surgeon
sitting up in bed
no IV yet
monitor
supplemental oxygen
rescue meds and equipment
ambubag
induction and airway in epiglottits
NO RSI: most likely NPO is okay bc of clinical course, risky if airway not obtained immemediately
SV with inhalational with child on parents lap
ensure adequate depth
then place IV
then intubate
difficult airway euquipment, help and surgeon ready
extubation criteria epiglottis
abx complete
24-48 hours
postive leak test
do in teh OR
surgeon drapped neck
fibreoptic view of airway
positive leak test
+ appropriate other
back to ICU after
induce FB aspiration
RSI can move FB to obstruct all ventilation so avoid
SV with inhaled ventilation
consider glyco/atropine in young populaiton to eliminte high vagal repsonse
Treat tet spell ToF
monitors
put knees to chest - increased SVR > want to decrease R to L shunt
Induce and airway TOF
want to maintain SVR and reduce PVR to promote less R to L shunting
- slow controlled with adequate oxygenation, ventilation
- blunt SNS with fentanyl, lidocaine
- ketamine to ensure SVR maintained
Maintenance anesthesia TOF
nitrous (volatiles promote PVR)
ketamine
oxygen