Smartdeck, 6.8 start Flashcards
most affective antipsychotic for treatment-resistant schizophrenia and schizoaffective disorder?
clozapine
most severe AEs of clozapine
agranulocytosis, seizures, myocarditis
compared to other antipsychotics, which one has the greatest risk of seizures?
clozapine
what actions are associated with risk reduction for long term rx opioid misuse?
state rx drug monitoring, random UDS, regular follow up
gold standard for evaluating risk in pt with hx of cervical surgery
transvaginal US
dysarthria, loss of DTRs, progressive gait and limb ataxia in adolescence
loss of position and vibratory senses
hypertrophic cardiomyopathy
friedreich ataxia
acute onset of ataxia, nystagmus, and dysarthria following an infection
acute cerebellar ataxia
musty odor urine
phenylketonuria
if PKU goes untreated…
intellectual disability and seizures
how to detect PKU
newborn screening
tandem mass spectrometry of dried blood spots
later in life - quantitative amino acid analysis
tx of PKU
dietary restriction of phenylalanine
how to differentiate hirschsprungs v meconium ileus
level of obstruction
Hirsh- rectosigmoid, normal consistency, positive squirt sign
mec ileus - ileum, inspissated consistency, negative squirt sign
bone pain and pancytopenia in a child
also fever, pallor, bruising, and hepatosplenomegaly
acute lymphoblastic leukemia
acute, unilateral cervical lymphadenitis in child is MCC by
S. aureus or S. pyogenes
pt has pna and developed signs of septic shock
airway is secure, what next?
IV normal saline
what is the MCC of community acquired bacterial meningitis
S. pneumo
can occur with or without concurrent pneumococcal pna
Vagal maneuvers will affect with node in the heart, AV or SA?
AV
High dose IV acyclovir can cause
crystalluria with renal tubular obstruction
diaphragmatic flattening in COPD caused by hyperinflation result in
increased work of breathing
intrinsic renal failure is commonly due to
acute tubular necrosis
high urine sodium
glomerulonephritis is characterized by
hematuria with RBCs
precocious puberty, normal bone age, really just increasing body hair
premature adrenarche
caused by early activation of adrenal androgens, more common in obsese children
profound hypoglycemia in pregnancy
acute fatty liver of pregnancy
management of acute fatty liver of pregnancy
immediate delivery
mucopurulent drainage with a friable cervix
acute cervicitis
management of hydatiform mole
DnC
serial bhCG post evacuation
contraception for 6 months
in adolescents, abnormal uterine bleeding is caused by
immature hypothalamic-pituitary-ovarian axis
causing irregular, heavy bleeding
in hemodynamically stable pt, acute uterine bleeding can be managed with
IV estrogen or high dose oral estrogen/progestin contraceptive pills
how long do you need pharmacotherapy for bipolar pt with multiple episodes?
likely life long
palpable lymph node, small/<2cm, soft, mobile nodes, localized to one area in a child or young adult
next step?
observation
tx for body dysmorphic disorder
SSRI and CBT
prerenal AKI is characterized by
low urinary sodium (<20)
low fractional excretion of sodium (<1%)
elevated BUN:Cr >20:1
urine sediment is bland
stable pt with wide complex tachycardia can be initially managed with
antiarrhythmics like amiodarone
daily copious mucopurulent sputum in pt with chronic cough
bronchiectasis
test to determine if Crohns or UC
colonoscopy
older adult with progressive neck pain, gait disturbances, lower motor neuron signs in UE, and UMN signs in LE
cervical spondylotic myelopathy
persistent, eczematous, and/or ulcerating rash is localized to the nipple and spreads to the areola
paget disease of the breast
what kind of cancer is associated with Paget disease of the breast?
adenocarcinoma
does primary syphilis have associated adenopathy
yes
mild to moderate LAD is often present
what causes granuloma inguinale?
klebsiella granulomatis
extensive, progressive, painless genital ulcers, usually without LAD
granuloma inguinale
infection causing vaginal pH <4
candida
normal pH is 3.8 -4.5
initial evaluation of mixed urinary incontinence
voiding diary
first line tx for primary dysmenorrhea
NSAIDs
physiologic change of pregnancy associated with insulin
increased insulin resistance due to increased levels of placental somatomammotropin
what is placental somatomammotropin?
human placental lactogen
what is the cause of labial adhesion?
if symptomatic, what is the tx?
low estrogen production
topical estrogen cream
side effect of oxytocin
similar to ADH, hyponatremia, seizure
Pts in preterm labor at <32 weeks require:
betamethasone (decrease risk neonatal RDS)
tocolytics/indomethacin
mag sulfate for fetal neuroprotection
what age can get vulvar lichen sclerosus
prepubertal girls and perimenopausal or postmenopausal women
tx vulvar lichen slcerosus
superpotent corticosteroid tx
in what age pt would you see labial adhesions?
<2 yo
high risk pts in pregnancy require what in third tri?
repeat testing for STIs
pregnant lady with pruritis worse on hands and feet; markedly elevated total bile acids
intrahepatic cholestasis of pregnancy
absent coagulation factor carboxylation
vit K deficiency
rupture of emissiary veins upon scalp traction during delivery
subgalel hemorrhage
diffuse fluctuant swelling extending beyond suture line in neonates
subgaleal hemorrhage
subperiosteal vessel rupture
cephalohematoma
firm, non fluctuant swelling, does not cross suture line in neonate
no significant blood loss
cephalohematoma
pressure of presenting part of the scalp against a dilating cervix
caput succadaneum
moderately dehydrated normal kid
IV normal saline
neonate with bruising after a home birth
vit K deficiency
reduced coagulation factor carboxylation
multiple infxns, S. aureus, Serratia, Burkholderia cepacia (catalase positive)
chronic granulomatous disease
umbilical cord fails to separate, decrease immune system
leukocyte adhesion deficiency
preterm, leukocytosis, metabolic acidosis, bilious vomiting
necrotizing enterocolitis
cyanosis in infant, bounding peripheral pulses, harsh systolic murmur at lower left sternal border, loud S2
truncus arteriosus
cyanosis, tachypnea, single loud S2
transposition of great vessels
defect in NADPH oxidase
chronic granulomatous disease
infecting organisms are catalase positive (S. aureus, E. coli, candida, klebs, pseudo, aspergillus, nocardia, serratia)
chronic granulomatous disease
diagnostic test for chronic granulomatous disease
dihydroorhodamine test
defect in neutrophil chemotaxis/microtubule polymerization
chediak higashi
oculocutaneous albinism, peripheral neuropathy, neutropenia
chediak higashi
coarse facies, abscesses, retained primary teeth, hyper IgE, dermatologic
Jobs syndrome
Hyper IgE
tx of hyper IgE syndrome
penicillinase-resistant abx and IVIG
recurrent neisseria infxns, rarely lupus or glomerulonephritis
MAC deficiency
tx for spascity of cerebral palsy
diazepam, dantrolene, baclofen
sepsis work up
CBC, UA, blood/urine/CSF culture
tongue fasiculations and symmetric proximal muscle weakness, greater in LE than UE
spinal muscular atrophy
young child with cervical paravertebral sympathetic chain LAD, droopy eyelid, constricted pupil, abdominal mass
neuroblastoma
elevated vanillylmandelic acid and homovanillic acid
neuroblastoma
3 yo presents with gross hematuria and painless right sided abdominal mass
wilms tumor
claw sign on abdominal mass imaging in kid
wilms tumor
kidney mass crossing midline on imaging
neuroblastoma
osteosarcoma (aka osteogenic sarcoma) is also associated with
Rb and Paget disease
predominantly cortical small tumor, severe nocturnal pain
dx and tx
osteoid osteoma
NSAIDs
where is osteoblastoma located?
spine
bony overgrowth of the hard palate
torus palatinus
lytic lesions in the skull, in child
langerhans cell histiocytosis
immune cells, langerhan histiocytes, tennis-raquet, bierbeck granules
most likely site of injury of clavicular fx
middle third of clavicle
overuse apophysitis
osgood schlatter
SCFE pt that is less than 10th percentile for height, get
TSH
kid with diet of mostly cheese and yogurt and drinks ridiculous amounts of milk
Fe deficiency anemia
ambiguous genitalia, super high testosterone, 46, XX
CAH
5 alpha reductase deficiency will be in what karyotype?
46 XY
aromatase deficiency will present with
virilization in both the fetus and the mom
failure to thrive, jaundice, hepatomegaly, infantile cataracts, neuro symptoms
galactosemia
excess urination in sickle cell trait
hyposthenuria
kidney cant concentrate urine
pt with friederich ataxia is most likely to die from
cardiac issue
calcified lesion in sella turcica in kid
craniopharyngioma
jaundice, pale stools, and dark urine during 2-8 weeks old
biliary atresia
amylase rich, exudative pleural effusion
pancreaticopleural fistula
decreased air flow during both inspiration and expiration, flattening the top and bottom of a flow loop is likely caused by
fixed upper airway lesion
sudden onset respiratory distress following removal of a central venous catheter
venous air embolism