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