Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
38 Cards in this Set
- Front
- Back
stridor is of what origin? stertor?
|
larynx trachea
nose, nasopharynx, oropharynx |
|
inspiratory stridor comes from? expiratory? biphasic?
|
supraglottis, glottis
trachea subglottis |
|
laryngomalacia accounts for what % of stridor in infants?
|
60%
|
|
what causes laryngomalacia
|
omega epiglottis
tall, foreshoretened AE folds redundant arytenoid mucosa, floppy then edema from mucosal trauma exacerbates sx. unproven cause, known association with higher rates of reflux |
|
what percentage of LM patients have synchronous airway lesions? what percentage require intervention
|
12-45%
5% |
|
what is the course of LM?
|
normal breathing at birth
develops stridor over days/weeks -2 months peak at 6-9 months resolves by 18 mo- 2 years worse when supine, with feeding, or with exertion cyanosis should prompt an airway eval for other lesions |
|
work up for LM
|
NP scope for dx
Cannot r/o other airway lesions until DL/B performed Sleep study in concerning cases for hypoxia and hypercapnea |
|
what are the indications for surgical intervention? ~10% of patients
|
severe stridor
cyanosis/hypoxia hypercapnea apnea pulmonary hypertension / cor pulmonale |
|
what might a supraglottoplasty entail? what are the risks of surgery?
|
(1) division of the aryepiglottic folds, (2) excision of a wedge of the aryepiglottic fold with or without trimming the arytenoids or the lateral border of the epiglottis, and (3) suturing of the epiglottis to the base of the tongue
risks: airway fire if laser, post op swelling, bleeding, aspiration, supraglottic scarring (interarytenoid region) |
|
Contrast ductal vs saccular cyst in the infant?
|
ductal - obstruction of duct, found anywhere in larynx, most commonly in supraglottis
saccular - congenital obstruction of space in the laryngeal ventricle, does not communicate with the laryngeal lumen treat both with unroofing or excision. |
|
What percentage of cases with congenital laryngeal abnormalities are vocal cord paralyses?
|
10% (contrast to LM as 60%)
M>F bilateral > unilateral |
|
What is the most common cause of VC paralysis? most common neurologic cause in peds?
|
idiopathic, congenital (usualy bilateral)
Neuro: Arnold chiari is most common neurologic abnormality (usually bialteral). Also encephalopathy and Guian Barre also birth trauma, intubation, head injury |
|
work up in peds for VC paralysis?
|
airway eval - palpate arytenoids and r/o other lesions, secure airway if distress
MRI brain to chest Swallow eval |
|
which is more likely to recover: acquired or congenital VC paralysis? unilateral or bilateral?
|
acquired
unilateral |
|
treatment for unilateral TVC paralysis in kids?
|
speech therapy. rarely trach.
|
|
treatment for bilateral TVC paralysis kids?
|
trach for airway.
serial endoscopies with no permanent interventions for 1 year - in case of spontaneous recovery |
|
why do laryngeal webs occur? how do you treat them?
|
failure of complete canalization of the trachea/larynx.
when severe is assoc with SG stenosis tx with excision of thin webs. laryngofissure, excision, and stent for thick webs |
|
what is the laryngeal cleft classification?
|
Classification of posterior laryngeal clefts. Type I: interarytenoid cleft; superior to the glottis. Type II: partial cricoid cleft; extends inferior to the glottis and partially through the posterior lamina of the cricoid. Type III: total cricoid cleft, with or without extension into the cervical tracheoesophageal wall. Type IV: laryngotracheoesophageal cleft extending beyond the thoracic inlet.
|
|
how are clefts diagnosed and treated?
|
dx: aspiration, video swallow, endoscopy
tx: open vs endoscopic closure if needed vs thickened feeds until swallow improves (type I) |
|
what is the strongest indicator of a laryngeal foreign body?
|
history
|
|
what is the key formula that explains why small changes in the pediatric airway result in croupy cough?
|
Poisioulle's law - airflow in a cylinder is directly proportional to the fourth power of the radius
|
|
explain how to calculate and determine SGS using the cotton myer grading system?
|
Grade is a %. Determined by largest possible ETT that can be passed / age appropriate tube size.
Grade 1 0-50% Grade 2 50-70% Grade 3 71-99% Grade 4 - no lumen |
|
congenital SGS is the ____ most common abnormality of the pediatric airway
|
3rd.
But acquired SGS accounts for 90% of SGS |
|
how does acquired SGS occurr? how can we prevent it?
|
pressure, necrosis, perichondritis, cicatricial scarring
smaller uncuffed tubes, extubate when able, nasotracheal intubation to avoid movement/friction |
|
SGS: diagnosis, treatment
|
dx: XR helps, endoscopy is gold standard and allows for grading
tx: monitoring (grade 1-2, allows for growth of child trach secures airway in symptomatic patient dilation airway recon LTR - anterior cric split - splits cric and first 2 tracheal rings with graft placement CTR - instead of widening the airway, we resect the stenotic segment - risk of RLN injury and dehiscence of anastamosis thermal damage from lasers can incite more scarring resulting in recurrent and worsened scarring |
|
6 month old female with stridor and a cutaneous red lesion on the scalp: what's the dx?
|
subglottic hemangioma
presents by 6 months of age. F > M 2:1 50% of SG hemangiomas have a cutaenous counterpart, usually in the head and neck |
|
what is the histology of a hemangioma?
|
most commonly capillary, but cavernous forms exist
is a vascular hamartoma (overgrowth/neoplasm of a particular tissue in it's tissue of origin) |
|
what are the phases of growth of a hemangioma?
|
12 months of proliferation, then years of involution
|
|
diagnosis?
|
x -ray may reveal asymetrically narrowed subglottis
needs DL/B for dx: unilateral, sessile, compressible, vascular lesion. Only biopsy if diagnosis is uncertain. Be prepared for bleeding. Need MRI for evaluation of neck and SG hemangiomas to r/o contiguous lesion |
|
treatment.
trach: discuss Risks and benefits steroids laser |
Trach: stabilizes airway until involution occurs. can affect speech and language development. Skilled home care needed incases of total upper a/w obstruction
steroids: systemic vs injection. can cause some swelling injection. get long term weight gain, growth retardation, hypertension, and cushingoid effects laser: can use Co2 and KTP. Might need repeat tx, risk of heat induced scarring excision: may avoid trach. may be used with other modalities. propanolol: not discussed |
|
whats the most common neoplasm of the larynx in children? how does it present?
|
RRP.
b/n 2-5 years, hoarseness, gradual onset of stridor increased risk if first born child of teenage mom needs multiple debridements at child onset is more aggressive than adult onset |
|
where do you see malignant transformation with RRP?
|
distal bronchial tree.
is rare, but ALWAYS sent path prognosis is poor |
|
Which type of HPV is more aggressive?
|
11> 6
|
|
goals of surgery
|
maintain an adequate airway while avoiding tracheotomy
preserving the voice controlling the papilloma Keys: leave small amt of papilloma to avoid scarring (particularly important with CO2 laser), masks needed with laser due to viral particles in air, avoid trach due to risk of distal spread, |
|
describe the presentation of Supraglottitis (epiglottitis)?
|
2-6 yo
possibly unvaccinated stridor - late finding with impending obstruction tripoding drooling muffled voice rapid onset febrile severe dysphagia no cough ddx: foreign body, RPA, |
|
treatment of epiglottitis?
|
Avoid stimulating the child
NP scope is ok if dx is unclear and there's no airway distress Xray can be used r/o other etiologies OR for intubation vs trach inhalational anesthesia for intubation (No IV) then culture blood and airway Ceftriaxone abx usually can exubate in 48-72 hrs. |
|
describe the presentation of laryngotracheobronchitis (croup)?
|
child between 6 months and 3 years
slow onset, barky cough, stridor, temperature swallowing fine. biphasic stridor indicates worsened prognosis. likely lasts 3-5 days, infectious with parainfluenza for 2 weeks. dx: clinical, but Xrays help treat: humidification, racemic epi, steroids (decreases hospital stay and need for intubation), heliox, ...intubation in 1.5% of cases |
|
whats the most common bug in bacterial tracheitis?
|
post viral staph aureus superinfection
x-ray and endoscopy show diffusely ulcerated tracheal mucosa with copious purulent secretions partially obstructing the lumen of the trachea. most patients need to be intubated. the, culture and direct abx. |