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57 Cards in this Set
- Front
- Back
which vasopressor:
causes renal vasodilation |
dopamine
|
|
which vasopressor:
high doses causes a1 vasoconstriction |
epinephrine
|
|
which vasopressor:
ADH analogue |
vasopressin
|
|
which vasopressor:
which vasopressor: DOC for anaphylactic shock |
Epi
|
|
which vasopressor:
DOC for septic shock |
NE
|
|
which vasopressor:
DOC for cardiogenic shock |
dobutamine
|
|
which vasopressor:
causes vasoconstriction but with bradycardia |
phenylephrine
|
|
med used to accelerate fetal lung maturity
|
betamethasone
|
|
how long is betamethasone given
|
48 hours
|
|
when does betamethasome stop working
|
>34 weeks
|
|
a/w red currant jelly stools
|
intussuception
|
|
features of measles
|
cough, coryza, conjuctivitis
koplik spots rash starts at head and spreads to feet |
|
Rx for measles
|
Vit A
|
|
features of rubella
|
fever
suboccipital and posterior cervical lymphadenopathy rash starts on face and generalizes polyarthritis |
|
features of coxsackie hand, foot, mouth disease
|
fever
oral vesicles on buccal mucosa and tongue rash on hands and feet (sometimes butt) |
|
features of scarlet fever by strep pyogenes
|
rash starts at trunk and generalizes, but spares palms and soles
-sandpaper like -sunburn like strawberry tongue desquamation of hands and feet |
|
features of roseola
|
fever
rash that starts when fever disappears erythematous papules on soft palate and uvula bulging anterior fontanelle |
|
causes of acute, bilateral cervical lymphadenitis
|
viral
|
|
causes of acute, unilateral cervical lymphadenitis
|
bacterial
-aureus -GBS |
|
causes of chronic unilateral cervical lymphadenitis
|
Bartonella
Tocoplasmosis TB Actinomyces |
|
causes of noninfectious cervical lymphadenitis
|
kawasaki
hodgkin lymphoma |
|
what is PFAPA syndrome
|
periodic fever
aphthous ulcer pharyngitis adenitis |
|
Rx for PFAPA syndrome
|
steroids
cimetidine |
|
what are the different stages of pertussis
|
incubation
catarrhal paroxysmal convalescent |
|
what happens in the catarrhal stage of pertussis
|
mild URI symptoms
|
|
what happens in paroxysmal stage of pertussis
|
inspiratory whoop
post-tussive emesis |
|
Rx for pertussis
|
azithromycin or erythromycin
isolation |
|
what is needed to work up in a child diagnosed with a UTI
|
voiding cystourethrogram
Renal US |
|
what are some causes of desquamation of the hands and feet
|
kawasaki
scarlet fever acrodynia TSST |
|
which viral infection is characterized by rash that appears when fever dissipates
|
roseola HHV-6
|
|
immunodeficiency characterized by:
no b cells in peripheral smear |
brutons
|
|
immunodeficiency characterized by:
defective tyrosine kinase |
brutons
|
|
immunodeficiency characterized by:
3 and 4 pouches fail to develop |
digeorge
|
|
immunodeficiency characterized by:
recurrent viral fungal and protozoal infection |
digeorge
|
|
immunodeficiency characterized by:
defect in early stem cell differentiation |
SCID
|
|
immunodeficiency characterized by:
cannot give live vaccines |
SCID
|
|
immunodeficiency characterized by:
triad: infection, diarrhea, failure to thrive |
SCID
|
|
immunodeficiency characterized by:
IgA deficiency |
ataxia telangiectasia
selective Ig Def (IgA is MC) |
|
immunodeficiency characterized by:
possible anaphylaxis to blood transfusions and blood products |
selective Ig Def
|
|
immunodeficiency characterized by:
lack of NADPH oxidase |
chronic granulomatous disease
|
|
immunodeficiency characterized by:
negative nitroblue tetrozolium dye |
chronic granulomatous disease
|
|
immunodeficiency characterized by:
prophylax with TMP-SMX and IFN-y |
chronic granulomatous disease
|
|
immunodeficiency characterized by:
defective LYST gene |
chediak higashi
|
|
immunodeficiency characterized by:
giant cytoplasmic granules in PMNs |
chediak higashi
|
|
immunodeficiency characterized by:
triad: albino, neuro disorder, recurrent respiratory and skin infection |
chediak higashi
|
|
immunodeficiency characterized by:
def in IFN-y |
job
|
|
immunodeficiency characterized by:
PMNs fail to respond to chemotactic stimuli |
Job
|
|
immunodeficiency characterized by:
triad:eczema, recurrent abcess, frontal bossing and doughy skin |
job
|
|
immunodeficiency characterized by:
retained primary teeth |
job
|
|
immunodeficiency characterized by:
abnormal integrins |
leukocyte adhesion deficiency
|
|
immunodeficiency characterized by:
congenital heart defect, low Ca, recurrent infection |
digeorge
|
|
immunodeficiency characterized by:
chronic mucocutaneous candidiasis, chronic diarrhea, failure to thrive |
SCID
|
|
immunodeficiency characterized by:
negatuve nitroblue tetrazolium |
chronic granulomatous
|
|
immunodeficiency characterized by:
poor pursuit of eyes, elevated AFP |
ataxia telangiectasia
|
|
immunodeficiency characterized by:
partial albinism, recurent URI and neuro disorder |
chediak higashi
|
|
when do infections start in children with immune deficiency
|
> 3 months
|
|
immunodeficiency characterized by:
what are the clinical features of wiskott aldrich |
thrombocytopenia
eczema recurrent infection |