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what are the steps for a blood transfusion for a pediatric patient
verify the childs identity
verify the donor type and compatibility
obtain baseline vitals
begin transfusion within 30 minutes of receiving blood
complete within 4 hours
remain w the child for 15 minutes
monito vs and child’s response
what to do if a transfusion reaction is suspected:
stop the transfusion
maintain IV access according to facility protocol
notify HCP
follow facility protocol
Iron deficiency anemia common causes;
inadequate iron intake
breastfeeding fter 6 months without adequate iron
premature
malabsorption
chronic blood loss
cows milk
s/s of iron deficiency anemia:
tachy
pallor
fatigue
irritability
weakness
systolic murmur
brittle nails
iron administration:
give 1 hour before or 2 hours after a meal
take with vitamin C
give with citrus if age appropriate
iron administration education
liquid iron can stain teeth
constipation
black stools are expected
iron fortified formula when indicated
limit formula to 32 o/day
sickle cell anemia
triggers RBC’s to become rigid and sickle shape
what can sickle cell anemia cause in the body
obstructed small vessels
increased blood viscosity
decreased circulation
tissue ischemia
pain and swelling
organ damage
clots
general findings of sickle cell anemia
fatigue
dizziness
SOB
pallor
pain
jaundice
hematuria
splenomegaly
recurrent infections
what are some sickle cell triggers
dehydration
infection
hypoxia
acidosis
physical and emotional stress
high altitudes
extreme temperatures
what are the different types of sickle cell crisis
vasocclusive
sequestrian
aplastic
acute chest syndrome
vasoclusive sickle cell crisis
sickled cells blocks circulation
s/s of vasoclusive sickle cell crisis:
severe pain
hematuria
jaundice
swelling
nc of svasoclusive sickle cell crisis:
asses pain
admin analgesics
provide oral and IV hydration
admin O2 of hypoxia
cool/warm packs
rest
sequestrain sickle cell crisis
blood pools mostly in the sleep
this is life threatening
s/s of sequestrain sickle cell crisis
enlarged spleen
hypovolemic shock
profound anemia
what are some s/s of hypovolemic shock
irritability
tachycardia
fever
decrease UO
cool extremities
thready pulse
hypotension
aplastic sickle cell crisis
RBCs drop dramatically
often triggered by viral infection
s/s of aplastic sickle cell crisis
profound anemia
pallor
lethargy
sleepiness
dyspnea
acute chest syndrome sickle cell crisis
presents like pneumonia
can lead to pulmonary hypertension
s/s of acute chest syndrome
chest pain
cough wheezing
fever
hypoxia
repeated episodes may cause pulmonary HTN
management of acute chest syndrome
aggressive treatment of infection
blood transfusion if needed
O2 and resp support
what do we give our sickle cell patients who are going through a crisis
pain meds
hydration
oxygen
rest
infection prevention
education
thalassemia characteristics (chronic anemia and hypoxia)
chronic anemia and hypoxia
Hbg life span is shortened
body produces Hgb rapidly
s/s of thalassemia:
failure to thrive
severe anemia
Hbg falls under 6
frontal bossing may occur
hemophilia
patient bleeds longer, clotting factors take a while to work
what are the two different types of hemophilia and what are some characteristics:
hemophillia a: 80% of all cases, in males, deficiency of factor VII
hemophillia b: 15% of all cases, deficiency of factor IX
s/s of hemophilia
bleeding tendicies ranging from mild to severe
hemarthritis → can lead to impaired movement
ecchymosis
epistasis
bleeding after procedures
diagnosis of hemophilia
amniocentesis
genetic testing
Hx and exam
labs
PTT will be prolonged; platelets may still be normal
management of hemophilia
replace missing clotting factors
DDVAP (hemophilia A)
PRICE (pressure, rest, ice, compress, elevation)
what are some education tips for hemophilia
shave only with an electric razor
apply press for 15 minutes
close supervision and safe environment