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56 Cards in this Set

  • Front
  • Back
Hirshprungs disease absecne of what
autonomic parasympathetic ganglion cells
HIsrchsprungs is common is what sex
male
Newborn failure to pass meconimum first 24 hours what DX
Hirshprunghs Disease
S/S of HIrsprungs
failure to pass stook. bile stained vomit, refusal to eat, abdomen distended
Hirsphrugns in infancy and childhoold what will you see
infancy constipation with explosive diahrria, Childhool Constipation with ribbon like stgools which smell foul, admomen distention, poor nourished child, anemic
NX interventions for Hirshprings pre op
rehydration,informed conscent, NPO, andno rectal tmep
post op Nrsg Interevengtion for Hirshpringus
Monitor site, bowel sounds, reheydrate, NG tube, parned education regarding colostomy
Hirshprungs Diseas may have temporarily what
colostomt
Plyoric stenosis rare in who
rare in black and asians
Pylosris strenosis more common in what sex
male
s/s pyloric stenosis
asymptomatic first 2 weeks of life, 2-4 wks regurgitation,6 week complete obstruction, projectile vomiting after feeding
failur to gian olive shaped mass right of unbilicus
pyloris stenosis
Nursing intervention pre op Pyloris stenosis
rehydration
Nsg Interventions Post op plyoric stenosos
slow feedeing upright position left side if needed
cystic fibrosis
inherite when both parents are carrier
cystic fibrosos what race
white both men and woman men, do better
cystic fibrosis
pulmonary involvement
cystic firbrosis sweat increased or decreased
increased
cystic fibrosis what type of lung sounds
non productive cough, wheezing, dyspnea, thick and sticky sputum
PKU foods to avoid
animal proteins ,meat, fish, eggs, milk, some vegtable proteings such as nuts, legume nutrasweet, aspertaime
tay sach disease what must both parents be to have child with disease
both parents must be carriers
tay sachs dx 1 in how many children will have dx
4
tay sachs how many out of 4 will be carrier
2
tay sachs life expectancy
5 yrs no cure
down syndrom look of children
occiptal flat, slanted eyes flat bridge of nose, small mouth, protuding tongue
out of 4 pregnancys wiht sickle cell how many will be normal and how many will have trait
one will be normal one will have trait if both parents are carriers
spina bifida
external saccular protrussion of any point along the spinal colum caused by failure of the nerual tube closure
surgery goal for spina bifida
not to reprair faulty spinal cord but to preserve existing function
spina bifida keep sac
moist and warm goal is to maintain sac no diaper until after repair and healing
post op spina bifida
monitor ICP neuro assessment, head circumfrance, infection
CHF classic signs
tachypena, tachycardia, dyspnea at rest, INCRASED LIVER SIZE VOLUME OVERLOAD, PRESSURE OVERLAOD, SEVERE ANEMAI, SEVERE SESISP, HYPERTHRYROIDISM , ELECTROLYTES IMBALANCE,
CHF S/S
EDEMA PHERIPHAL
TX CHF
CONSERVE ENERGY, UP RIGH AND ON SIDE TO SLEEP, PROTUGUESE SLING , FEEDING TAKE UP TO ONE HOUR, TREAT INFECTIONS, MAINTAINE ROOM TEMP NOT TO HOT NOT TO COLD
WHY GIVE DIG
TO IMPROVE MYOCARDIA CONTRACTILITY, INPROVE OUT PUT AND INCREASE RENAL FUNCTION
KYPOKALEMIA INCREASE RISK OF WHAT TOXICITY
DIG
S/S DIG TOX
MUSLCLE SPASMS, TWITCHING
ACEINHIBITORS PRODUCE
AFTER LOAD AND DECREASESWORK ON HEART TO IMPROVE CARDIAC FUNCTION
CAPTON AND VASOTEC USED FOR
CHF
HEMOPHILLIA A CLASSIC FACTOR
8 DEFECT
HEMOPHILLIA B CHRISTMAS DISEASE
FACTOR 9 DEFECT
HEMOPHELLIA WHO IS CARRIER
MOTHER AND PASSES TO SON
WHAT IS MOST COMMON POSITION FOR TERATOLOGY OF FALLOT
KNEE CHEST
FACTOR 8
HUMAFAC OR KOATE
FACTORY 9
PROLOX OR KONYNE
TRACHEALESPHOGUIAL FISTULA
COUGH, CYNOSIS , CHOCKING (3'S)
HIP DYSPLAISS WHAT WILL YOU SEE
HIP WRINKLNG
atropine
block vague stimulus resulting in increased heart rate
calan (vermapamil)
channel blocker will decrease heart rate
quinidine
an antidysrythmic used for tachyarrythmias
hodgikins diseas
neoplastic disease that is characterized by prgression enlargement of lymph nodes, spleen, and liver bhy prgressive anemail
hirschsprungs dx
involves and absence in the autonomic ganglia of the smooth muscle in a section of the colon
myelomeningocele
sac like protrusion outside the bodyand contains CSF adn mengies
meningocele
sac containing CSF and may containmengies but not neural tissue
cyctole
hernia of bladder
RIGHT SIDED HEART FAILURE
PULMONARY HTN, PULMONARY EMBOLISIM, CHD ( VENTRICAULR SEPTAL DEFECT, PATENT DUCTUS ARTERIOUSUS
LEFT HEART FAILURE
MYCOCARDIDTISIS, AMLYDISIS