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no cyanosis
non-life-threatening congenital disorders
can delay surgery
ACYANOTIC HEART DEFECTS
with cyanosis, purplish or bluish in color
life-threatening congenital anomaly
poor supply of oxygenated blood
a medical emergency and needs surgery
CYANOTIC HEART DEFECTS
failure of the ductus arteriosus to close at birth or within the first week of life
can be asymptomatic
MURMUR: ____
increased workload in the left side of the heart
due to decreased systemic circulation, ____ compensates
has pulmonary vascular congestion due to increased blood flow resulting to ____
which is a protective mechanism leading to a complication known as ____
MEDICAL MANAGEMENT: ____ AND ____
SURGICAL MANAGEMENT: ____ WHEN: ____ if (+) s/sx; ___ if (-) s/sx
PATENT DUCTUS ARTERIOSUS
MACHINERY-LIKE MURMUR
LEFT VENTRICLE
INCREASED PULMONARY VASCULAR RESISTANCE
PULMONARY VASCULAR OBSTRUCTIVE DISEASE
INDOMETHACIN, IBUPROFEN
LEFT THORACOTOMY, BEFORE 6 MOS, BEFORE 1 YR
narrowing of the aorta → less oxygenated blood in systemic circulation → compensatory mechanism
MANIFESTATIONS:
UPPER EX: ___, ___
LOWER EX: diminished pulse, low BP, cool to touch, pallor, numbness and tingling (___)
COMPLICATIONS: ___, ___, CVA
NON-INVASIVE MNG: ___ minimally invasive procedure using the ___ artery
SURGICAL MNG: ___ to prevent bleeding and hemorrhage
COARCTATION OF THE AORTA
BOUNDING PULSE, HIGH BP
PARESTHESIA
AORTIC ANEURYSM, RUPTURED AORTA
BALLOON ANGIOPLASTY, FEMORAL
SURGICAL REPAIR
patent foramen ovale
hole in between the R and L atrium
vena cava → RA → RV → PA → PV → LA → RA → RV → congestion of the R
MANIFESTATIONS: ____
COMPLICATIONS: Heart failure, atrial dysrhythmia, emboli formation → ___
SURGICAL MNG: Surgical patch closure ____, ____
ATRIAL SEPTAL DEFECT
RIGHT VENTRICLE HYPERTROPHY
PULMONARY VASCULAR OBSTRUCTIVE DISEASE
DACRON PATCH, PERICARDIAL PATCH
hole in between R and L ventricle
same mechanism in ASD
COMPLICATIONS: ___ due to friction
20-30% of this case closes spontaneously during the ___ of life
SURGICAL MANAGEMENT: ____ to protect the lungs, patch
VENTRICULAR SEPTAL DEFECT
BACTERIAL ENDOCARDITIS
1ST YEAR
PULMONARY ARTERY BANDING
narrowing of the pulmonary valve
RA → RV → PA → due to narrowing, decreased blood flow to lungs → RV
MURMUR: ___
MANIFESTATIONS: RVH, dyspnea, signs of HF, mild cyanosis
NON-SURGICAL: ___
SURGICAL: ___
PULMONARY STENOSIS
2ND ICS L
BALLOON ANGIOPLASTY
PULMONARY VALVOTOMY
narrowing of the aortic valve
LA → LV → AORTA → narrowing pushes back blood to the left side of the heart → ____ that interferes with ____ that can lead to ____
COMP MECH: ____
chest pain due to ____
MURMUR: ____
brain hypoperfusion
SURGICAL: ___, ___, ___
AORTIC STENOSIS
LEFT VENTRICULAR HYPERTROPHY, CORONARY ARTERY PERFUSION, MI
TACHYCARDIA
ISCHEMIA
2ND ICS R
AORTIC VALVOTOMY, AORTIC VALVULOPLASTY, AORTIC VALVE REPLACEMENT
RV is connected to aorta, LV is connected to pulmonary artery
___ keeps the patient alive due to blood mixing with the DOC of ___
MANAGEMENT:
Oxygen therapy: __-__ L/min
avoid overfeeding and constrictive clothing
SURGICAL:
___ surgical procedure to create PDA
___ opening the atrial septum to promote blood mixing
___ complete repair of the vessels
TRANSPOSITION OF THE GREAT ARTERIES
PDA, ALPROSTADIL
6-8
BLALOCK-HANLON OPERATION
BALLOON ATRIAL SEPTOSTOMY/RASHKIND PROCEDURE
JATENE OPERATION
4 heart problems
___ primary problem
___ comp mech
___ causes blood mixing
___ keeps the patient alive
cyanosis observed on distal ends of ext, nail beds, lips, tongue
tet spell
___ test used for clubbing of fingers
MANAGEMENT:
POSITIONING: ___, ___
100% O2
calm comforting approach
DOC: ___
SURGICAL:
___ supplies blood to the pulmonary artery from the ___ to increase pulmonary blood flow
COMPLETE REPAIR
IMPRATUBE GRAFT/GORTEX
PULMONARY STENOSIS
RVH
OVERRIDING AORTA
VSD
SCHAMROTH WINDOW TEST
SQUATTING, TRIPOD; KNEE-CHEST POSITION
MORPHINE
MODIFIED BLALOCK TAUSSIG SHUNT OPERATION, SUBCLAVIAN ARTERY
___ infection of the inner lining of the heart which is the ___
generally involving the valves specifically the ___
occurs secondary to bacteremia which is caused by invasive procedures
CA:
MOST COMMON: ___, ___
CANDIDA ALBICANS
MANAGEMENT:
___ long term management via IV
___ positioning
PREVENTION:
prophylactic antibiotics prior to invasive procedures usually ___ the procedure
BACTERIAL ENDOCARDITIS, ENDOCARDIUM
MITRAL VALVE
STAPHYLOCOCCUS AUREUS, VIRIDIANS
ANTIBIOTICS
ORTHOPNEIC
1 HR BEFORE
___ inflammatory disease that occurs after GABHS infection
onset ___ following GABHS infection
commonly affects ___ children
areas of concern: ___, ___, ___, ___
cause: ___
DIAGNOSTIC: ___ most reliable and standardized evaluation
MAJOR JONES CRITERIA: ___, ___, ___, ___, ___
MINOR JONES CRITERIA: ___, fever, elevated ESR, elevated CRP, prolonged PR interval
MANAGEMENT:
___ anitbiotic
___ salicylates
COMPLICATION: ___ with permanent damage to the ___ valves
RHEUMATIC FEVER
-
SCHOOL AGE
BRAIN, HEART, JOINTS, SKIN
UNMANAGED URTI
CARDITIS, POLYARTHRITIS, ERYTHEMA MARGINATUM, CHOREA, SUBCUTANEOUS NODULES
ARTHRALGIA
PENICILLIN
ASPIRIN
RHEUMATIC HEART DISEASE, CARDIAC
unknown systemic vasculitis (destructive inflammation of the blood vessels); idiopathic
commonly affects ___
areas of concern: ___
MANIFESTATIONS: extensive inflammation of the ___, ___, ___ during acute phase
prolonged elevated temp not attributed to another cause and unresponsive to antibiotics
goal is to prevent ___ complications
COMPLICATIONS: ___ (aneurysm), ___ (mi)
MEDICAL MANAGEMENT:
high dose of ___
salicylate therapy: ___
___ to prevent thrombus formation
KAWASAKI DISEASE/MUCOCUTANEOUS LYMPH NODE SYNDROME
TODDLERS
CARDIOVASCULAR SYSTEM
ARTERIOLES, VENULES, CAPILLARIES
CARDIOVASCULAR
DILATED CORONARY ARTERY, CORONARY THROMBOSIS
IV GABBA GLOBULIN
ANTIPLATETLETS
ABCIXIMAB
3 phases of kawasaki disease
ACUTE
SUBACUTE
CONVALESCENT
this phase of KD,
abrupt onset of high fever: ___
child is very irritable
tongue is called ____
___ rashes with variety of shapes
conjunctival hyperemia/bilateral conjunctivitis leads to ___
ACUTE
38.5 DEGC AND ABOVE
STRAWBERRY TONGUE
POLYMORPHOUS RASH
PHOTOSENSITIVITY
this phase of KD,
resolution of fever
high risk for: ___ seen on ___
___ peeling of the hands and feet during the ___ - ___ week; use ___
cracked lips, use lubricating ointment
SUBACUTE
CORONARY ARTERY ANEURYSM, ECHOCARDIOGRAM
PERIUNGUAL DESQUAMATION, 2ND - 3RD, UNSCENTED LOTIONS
this phase of KD,
the recovery phase usually on the __-__ weeks after onset
all clinical signs are resolved
regained usual temp, energy, and appetite
CONVALESCENT
6TH TO 8TH
nosebleed
most common cause is ___
MANAGEMENT:
Lean: ___
Apply pressure: ___ for at least ___ mins
Cold compress for vasoconstriction not more than __ mins
EPISTAXIS
TRAUMA
FORWARD
SOFT TISSUES OF THE NOSE, 5 MINS
20 MINS
deficiency in clotting factor which results to bleeding
FEMALE: ___, MALE: ___
MANIFESTATIONS: easy bruising, prolonged bleeding time (N: _-_ mins), trauma, ___ (bleeding joints, use RICE), ___ (classic sign)
MANAGEMENT: ___, bleeding precautions: avoid ___ sports, use ___ toothbrush, use ___ razor
HEMOPHILIA
CARRIER, MANIFESTS THE DISEASE
1-10 MINS, HEMARTHROSIS, SPONTANEOUS HEMATURIA
CRYOPRECIPITATE, CONTACT, SOFT BRISTLES, ELECTRIC
clAssic hemophilia
HEMOPHILIA A, CF 8
christmas disease
HEMOPHILIA B, CF 9
ros(C)ental syndrome
HEMOPHILIA C, CF 11
inability of the platelets to adhere which causes excessive bleeding
problem is ___
VON WILLEBRAND DISEASE
___ supports the production of hemoglobin
AT RISK:
___ d/t inadequate iron stores; the storage of iron in the liver and bone marrow starts at ___ of gestation
___ d/t poor eating habits, menstruation
MANAGEMENT: iron rich foods, oral iron supplements: ___ for ___ months
antidote for iron toxicity: ___
if in liquid form, use ___, ___, ___
do not store for more than a ___
IRON
PRETERM, 8TH MONTH
ADOLESCENTS
FERROUS SULFATE, 3 MONTHS
DEFEROXAMINE
STRAW, SYRINGE, DROPPER
MONTH
irregular shaped RBC: ___ (N: ___) d/t presence of ___
___ carrier of oxygenated blood
MANIFESTATIONS: underweight, chronic anemia, fatigue, severe pain
MANAGEMENT: hydration, oxygen therapy, ___ (antimetabolite)
SICKLE CELL ANEMIA
CRESCENT, BICONCAVE, HBS GENE
RBC
HYDROXYUREA
extra chromosome at the 21st chromosome (___)
normal no. of chromosomes: ___ (__ pairs)
MANIFESTATIONS:
large protruding tongue which leads to difficulty of ___ → ___ → ___
VSD
mental retardation → specialized ___
DOWN SYNDROME
46, 23
FEEDING, MALNUTRITION, DEATH
EDUCATION
inflammation of the meninges which is the membrane that covers the brain and spinal cord. it also supports the brain
inflammation of the brain
MENINGITIS
ENCEPHALITIS
manifestations of meningitis:
irritability
high pitched cry or ____
projectile vomiting
seizure due to ____
nuchal rigidity or ____
____ flexion of the knees → hamstring pain
____ flexion of the neck → flexion of the knee
____ exaggerated arching of the back; intervention is ____
SHRILL
INCREASED ICP
STIFF NECK
KERNIG’S SIGN
BRUDZINSKI’S SIGN
OPISTHOTONUS; SIDE LYING POSITION
causative agent of meningitis: ____
____ most common
haemophilus influenzae; prevention is ____
streptococcus pneumoniae
BACTERIA
NEISSERIA MENINGITIDIS
HIB VACCINATION (PENTAVALENT)
diagnostics of meningitis:____ between __ and __
contraindicated in ___ because it can lead to ___
immobilize the child
during: ___ position
after: ___ to prevent spinal headache
LUMBAR PUNCTURE/LUMBAR/SPINAL TAP; L4 AND L5
INCREASED ICP; BRAIN HERNIATION
FETAL
FLAT ON BED
enlarged ventricles due to overproduction of CSF by the ____ and underabsorption of the ____
this type is due to the obstruction such as tumor growth
HYDROCEPHALUS; CHOROID PLEXUS; ARACHNOID VILLI
NON-COMMUNICATING HYDROCEPHALUS
manifestations:
head enlargement
bossing forehead
bulging fonatenelles
dilated scalp veins
sunset eyes which is a ____
increased ICP (N: ___)
irritability
shrill
ALOC
projectile vomiting
cushing’s triad (___, ___, ___)
LATE SIGN
<15 MMHG
HYPERTENSION, BRADYCARDIA, BRADYPNIA
management of hydrocephalus
____
____
support the neck and head
skin care to moisturize. do not use alcohol and scented
VENTRICULOPERINOTAL SHUNT
TUMOR RESECTION
due to high fever which is ___ deg c
immaturity of the hypothalamus
FEBRILE SEIZURE
>= 38.5
management of febrile seizure:
seizure precaution
anticonvulsants: ____
never stop abruptly!!! as it can cause ____, taper only
use soft-bristled toothbrush for oral care to prevent ____
PHENYTOIN (DILANTIN)
STATUS EPILEPTICUS
GINGIVAL HYPERPLASIA
during seizure episode:
promote ___ by removing pillows and raising side rails
maintain ___ by side-lying/lateral position
SAFETY
PATENT AIRWAY
failure of the spine to fuse at the center
deficiency in ____
NEURAL TUBE DEFECTS
FOLIC ACID (VITAMIN B9)
absence of the skull
ANENCEPHALY
this neural tube defect:
(-) sac
(+) skin depression/dimpling
(+) dark tuffs of hair
(-) paralysis
(+) weakness
(-) alterations in bowel and bladder function
frequently no observable manifestations
no surgery needed
complications:
short term: ___
long term: ___
SPINA BIFIDA OCCULTA
MENINGITIS
HYDROCEPHALUS
this neural tube defect:
(+) sac
(+) paralysis
(+) alteration in bowel and bladder function
incontinence
urine dribbling
____ with spinal cord
____ pure CSF
management:
prevent damage of the sac by prone position with no diapers and apply sterile, moist, and non occlusive dressing
SPINA BIFIDA CYSTICA
MYELOMENINGOCELE
MENINGOCELE
a birth defect characterized by absence of extremities
cause by ____ drug such as ___
AMELIA
ANTIEMETIC DRUGS; THALIDOMIDE
common in male
problem is poor sucking ability → malnutrition (_INTERVENTION_) and aspiration (_INTERVENTION_)
high risk for infection
surgery: ____ at 2 months
CLEFT LIP
CROSS CUT NIPPLE; FEED IN UPRIGHT
CHEILOPLASTY
common in female
problem is speech
surgery:___ at 12-18 months
CLEFT PALATE
PALATOPLASTY
failure of the esophagus to develop as a continuous passage
manifestations:
coughing
choking
cyanosis
management:
maintain patent airway
prevention of pneumonia
surgical repair
ESOPHAGEAL ATRESIA
failure of the trachea and esophagus to separate
manifestations:
coughing
choking
cyanosis
management:
maintain patent airway
prevention of pneumonia
surgical repair
TRACHEOESOPHAGEAL FISTULA
narrowing of the pylorus
thickening of the pyloric sphincter
manifestations:
upper abdominal distention
projectile vomiting
vomitus: ___
signs of dehydration
metabolic ___
malnutrition and weight loss
visible peristaltic movement from L to R
_____ mass in RUQ
management:
increase oral fluid intake
assess the vomitus
high fowlers to avoid gas forming foods
HYOPERTROPHIC PYLORIC STENOSIS
diagnostic of hypertrophic pyloric stenosis
surgery: ___
ABDOMINAL ULTRASOUND
PYLOROTOMY
telescoping of the colon
site: ____ boundary of the small and large intestine
manifestations:
sudden abdominal pain: ____
abdominal distention
_____ stool
_____ mass
management:
assess borborygmus
assess abdominal distention
NGT insertion
passage of a ____ stool indicates that the intussusception has reduced
INTUSSUSCEPTION
ILEOCECAL VALVE
COLICKY
RED CURRANT JELLY STOOL
SAUSAGE-SHAPED MASS
diagnostic of intussusception: ____ confirmatory, barium enema, ____ (fecal occult blood test)
before the procedure:
avoid intake of ____, dark colored foods, ___, NSAIDS
surgery: ____ resection of the colon
UTZ, GUAIAC’S TEST
VITAMIN C, IRON
LAPAROTOMY
____ is the absence of ____ which is a nerve essential for peristalsis and nutrient absorption
it is also known as aganglionic megacolon
stool is ____
manifestations:
(-) peristalsis
enlarged colon
____ mass
bile-stained foul smelling emesis
foul breath
malnutrition
HIRSCHPRUNG’S DISEASE, GANGLION
RIBBON-LIKE STOOL, PENCIL-SHAPED, STRING-LIKE
FECAL-SHAPED
diagnostic for aganglionic megacolon
surgery: ___
management:
high calorie diet
assess the stoma
N:___ color
AB:___ color → necrosis → report!
colostomy care:
size: ___ larger than the stoma
epmtying: __ - __ full
RECTAL BIOPSY
SWENSON PULL-THROUGH
PINKISH
BLUISH/GRAY
1/8
1/3-1/2
gluten intolerance
manifestations:
diarrhea
steatorrhea
malnutrition
severe abdominal distention
complication: malignant ____ of the small intestines
CELIAC DISEASE
LYMPHOMA
management of celiac disease:
avoid foods with gluten
do not consume BROW (___, ___, ___, ___)
diagnostic: ____ confirmatory
BARLEY, RYE, OAT, WHEAT
BIOPSY
all secretions are viscous
organs affected: ___, ___, ___, ___
manifestations
meconium ileus
thick bronchial secretions
difficulty breathing
very salty sweat
acute pancreatitis d/t ____
CYSTIC FIBROSIS
INTESTINES, LUNGS, SKIN, PANCREAS
OTTODIGESTION
management of cystic fibrosis:
_____ with doctor’s order
pancreatic enzymes after meals
complications:
female: ___
male: ___
CHEST PHYSIOTHERAPY
DECREASED FERTILITY
STERILITY
caused by extrinsic allergens
____ → bronchoconstriction
____ → swelling of goblet cells
O2 and CO2 are _____ proportional
manifestations:
dyspnea
use of accessory muscles
hyperventilation
initially: respiratory ____
late: respiratory ____
management:
positioning: ____
brochodilators: ____
oxygen
corticosteroids: ____
BRONCHIAL ASTHMA
LEUKOTRINES
HISTAMINE
INVERSELY
ALKALOSIS
ACIDOSIS
ORTHOPNEIC
ALBUTEROL
BECLOMETHASONE
____ is the inflammation of the tonsils cause by too much ____ which attracts microbes
CA: ____
manifestations:
hyperthermia
dysphagia
complications:
bacteremia
endocarditis
management:
antibiotics
increase oral fluid intake
gargling solutions
criteria: 3-5x a year
surgery: ___, post-op: ___
TONSILITIS
GLUCOSE
GROUP A BETA HEMOLYTIC STREPTOCOCCUS
___ is the inflammation of the adenoids caused by ____ weather
manifestations:
hyperthermia
dysphagia
complications:
bacteremia
endocarditis
management:
antibiotics
increase oral fluid intake
gargling solutions
criteria: 3-5x a year
surgery: ___
ADENOIDITIS, COLD
ADENOIDECTOMY
manifestations:
hyperthermia
oliguria
periorbital edema
hematuria
hypertension
management:
constant monitoring of BP: ___
loop diuretics: ____
ACUTE GLOMERULONEPHRITIS
EVERY 4 HRS
FUROSEMIDE
this is caused by e. coli which is a bacteria
common in female because their urethra is shorter (__-__ inches)
manifestations:
dysuria
cloudy urine
hyoerthermia
complications:
cystitis
pyelonephritis
UTI
2-3 INCHES
protein-losing nephropathy
prevalence: ___-___ y/o in male
causes:
idiopathic/childhood npehrosis
secondary to glomerular damage
recessive disorder
diagnostics:
urinalysis (+) protein
blood test
____ confirmatory
NEPHROTIC SYNDROME
2-7
RENAL BIOPSY
manifestations of nephrotic syndrome:
massive ____
frothy and cloudy urine
recurrent infections d/t loss of _____
hypercoagulability d/t loss of _____
hypoalbuminemia
hyperlipidemia
protein is essential to maintain: ____
complications:
circulatory collapse
thromboembolism
management:
low sodium diet
high-biological protein diet
fluid restriction
corticosteroids: ____
prevention of infection
PROTEINURIA
IMMUNOGLOBULINS
ANTITHROMBIN III
ONCOTIC PRESSURE
PREDNISONE
a cancer originated in kidneys
management:
constant monitoring of BP
avoid abdominal pressure
manifestations:
abdominal mass (never palpate!)
painless hematuria
high blood pressure
general manifestations of cancer
WILM’S TUMOR