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41 Cards in this Set

  • Front
  • Back
croup
bug --> parainfluenza
presentation --> barking cough, hoarseness, inspiratory stridor
diagnosis --> clinical
treatment --> warm moist, nebulized epi, corticosteroids
complications --> hypoxia
epiglotitis
bug --> strep pyogenes, strep neumoniae, staph, mycoplasma
medical emergency
presentation --> sudden onset high fever, difficulty swalloing, drooling, toxic-appearance, stridor
diagnosis --> clinical looking cherry-red swollen epiglotis
treatment --> consult ENT and intubate + antibiotics
complications --> death
bacterial tracheitis
bug --> staph
presentation --> brassy cough, high fever, respiratory distress, no drooling or dysphagia
diagnosis --> clinical + laryngoscopy
complicaions --> airway obstruction
spasmodic croup
bug --> viral
presentation --> coryza and hoarseness + sudden onset afebrile croup-like; improves within hours, lasts 2-3 days
diagnosis --> clinical
treatment --> supportive
acute infecitous laryngitis
bug --> diptheria
presentation --> hoarseness and loss of voice out of proportion to systemic findings, sore throat
differential diagnosis of upper airway obstruction
croup
epiglotitis
bacterial tracheitis
spasmodic croup
acute infectious laryngitis
foreign body aspiration
retropharyngeal abscess
extrinsic compression
angioedema
laryngomalacia
congenital anomaly presents with stridor at 2 weeks of life
MCC of stridor
clinical suspicion confirmed with laryngoscopy
treat with surgery
congenital subglottic stenosis
recurrent persistent croup
2nd MCC of stridor
initial test --> x-ray
confirm --> laryngoscopy
surgery
vocal cord paralysis
associated with meningomyelocele, Chiari, hydrocephalus or acquired
bilateral --> airway obstruction
unilateral --> aspiration, cough, choking, weak cry
diagnosis --> flexible brnchoscopy
resolves in 6-12 months; may require temporal tracheostomy
airway foreign body
presentation --> acute choking, coughing, wheezing, respiratory distress, decreased breath sounds
diagnosis --> chest x-ray reveals air trapping; confirm with bronchoscopy
therapy --> removal by bronchoscopy
acute bronchitis
presentation --> dry hacking persistent cough may be purulent; coarse and fine crackles
differential --> exclude pneumonia
treatment --> supportive
bronchiolitis
bug --> RSV (50%), parainfluenza, adenovirus, mycoplasma
presentation --> paroxysmal wheezy cough, dyspnea, tachypnea, apnea, fine crackles; most common in <2y/o
diagnosis --> clinical; chest x-ray shows patchy atelectasis
treatment --> supportive care +- beta2-agonist; no steroids
small airway diseases
bronchiolitis
acute bronchitis
stridor differential diagnosis
laryngomalacia
congenital subglottic stenosis
vocal cord paralysis
croup
upper respiratory infection diffferenatial
croup
acute infectious laryngitis
acute bronchitis
bronchiolitis
pneumonia etiology
0-28 days --> GBS, gram-, listeria
3 wk- 3 mo --> C. trachomatis, RSV, parainfluenza
4 mo-4 y --> viruses; RSV; parainfluenza, influenza, adenovirus
>5 y/o --> bacteria; mycoplasma, pneumocococcus, C. pneumoniae
viral Vs bacterial pneumonia
onset --> acute in bacterial; several days of URI in viral
temperature --> very high in bacterial
URI --> present in viral
toxicity --> bacterial
rales --> scattered in viral; localized in bacterial
WBC --> increased in bacterial
chest x-ray --> streaking in viral; lobar in bacterial
pneumonia diagnosis
clinical + x-ray + WBC
definitive --> isolation of virus or antigens in respiratory secretions for viruses; blood culture, pleural fluid or lung for bacteria (not sputum)
x-ray in pneumonia
viral --> hyperinflation with bilateral interstitial infiltrates and peribronchial cuffing
pneumococus --> lobar consolidation
mycoplasma or chlamydia pneumoniae --> unilateral lower-lobe interstitial pneumonia looks worse than presentation
chlamydia trachomatis pneumonia
1-3 months
no fever or wheezing
staccato cough
eosinophilia
pneumonia treatment
empiric amoxicillin for outpatient mild cases
empiric parenteral cefuroxime for hospitalized
if viral --> withold treatment if mild; if worsens add antibiotics
for mycoplasma of chlamydia --> erythromycin
cystic fibrosis pathogenesis
mutation of CFTR gene renders epithelial cells incapable of secreting chloride with failure to clar mucous secretions produced
systems mostly affected by cystic fibrosis
respiratory tract
pancreas
intestical glands
genitourinary tract
intestinal manifestations of cystic fibrosis
meconium ileus --> in 15-20% of newborns (dilated loops with air fluid levels and ground glass on x-ray)
pancreatic insufficiency --> malabsorption with failure to thrive, frequent bulky greasy stools, ADEK deficiency, DM, pancreatitis
hepatobilliary --> obstruction leads to icterus, ascites hepatomegaly
rectal prolapse
respiratory manifestations of cystic fibrosis
presentation --> cough and purulent mucus (bronchiectasis), PFT abnormalities, cor pulmonale, death
exam --> increased A-P diameterhyperresonance, rales, clubbing, expiratory wheezing
genitourinary presentation of cystic fibrosis
delayed sexual development
azoospermia, hernias, hydrocele, cryptorchidia
secondary amenorrhea, cervicitis, infertility
cystic fibrosis diagnosis
best test --> two sweat tests > 60mEq/L
pancreatic tests --> 72-hour fecal fat collection, trypsin in stools
PFT --> obstructive by 5 years then restrictive
micro --> staph and pseudomonas in sputum
genetic testing
newborn screen
newborn screen for cystic fibrosis
1) immunoreactive trypsinogen in blood
2) confirmation with sweat or DNA testing
cystic fibrosis management
clear airways --> salbutamol saline aerosol + human recombinant DNAse (mucolytic); chest physical therapy
antibiotics --> tobramycin (outpatient); tobramycin + piperacillin (inpatient)
ibuprofen slows disease; no steroids
nutritional --> pancreatic enzymes + ADEK vitamins
sudden infant death syndrome definition
sudden death unexplained by autopsy, forensics or medical history
sudden infant death syndrome differential diagnosis
infections
congenital anomaly
unintentional injury
trumatic child abuse
intentional suffocation
sudden infant death syndrome reduction of risk
supine while sleep
cribs with safety standards
no soft surfaces or bedding
avoid overheating
asthma presentation
diffuese wheezing, expiratory then inspiratory
prolonged expiratory phase
decreased breath sounds
accesory muscles
tachypnea
rales/bronchi
increased work of breathing
asthma diagnosis
clinical diagnosis in children
lab tests and provocation tests are not required but may be used to follow patient
LFT --> gold standard; FEV1/FVC <0.8 with improved FEV1 after beta agonist
images --> hyperinflation and flattening of diaphragms; peribronchial thickening
mild intermittent asthma
daytime --> <2x/week
nightime --> >2x/month
PFT --> FEV1 >= 80%
treatment --> short-acting beta agonist (albuterol, levalbuterol)
mild persistent asthma
daytime >= 2x/week
nightime >= 2x/month
PFT --> FEV1 >= 80%
treatment --> inhaled steroids + beta agonist for breakthrough
moderate persistent asthma
daytime --> daily
nightime --> >1x/week
PFT --> FEV1 60-80%
treatment --> inhaled steroids + long-acting beta agonist (salmeterol) +- short-acting beta agonist for breakthrough
severe persistent asthma
daytime --> continually; limited activities
nightime --> frequent
LFT --> <= 60%
treatment --> high-dose inhaled steroid + salmeterol (long-acting) + albuterol + systemic steroids
asthma rapid-onset medications
beta 2 agonists --> albuterol, levalbuterol (inhaled)
anticholinergics --> ipratropium (less potent than beta 2; use as add-on)
long-term asthma medications
NSAID --> cromolyn; mild-moderate asthma; alternative
long-acting beta agonists --> salmeterol; used in ICS
inhaled corticosteroids --> 1st gen: beclomethasone, flunisolide, triamcinolone; 2nd gen: budesonide, fluticasone, mometasone
leukotrienes --> inhibitors: zileuton; antagonists: montelukast, zafirlukast
systemic steroids --> prednisone, prednisolone
emergency management of asthma
O2
inhaled albuterol +- ipratropium +- corticosteroids PO/IV
go home if sustained improvement, SaO2 > 92% after 4 hours in room air
if no improvement --> hospitalize and add IV steroids