Blood Flashcards
blood functions
O2/nutrient transport
clots
cells/antibodies to fight infection
brings waste to kidneys
supports water/electroly balance (pH mx)
regulated body temp/hormone circ
blood components
plasma - 55%
platelets
WBC
RBC - 44%
plasma function
coagulation
defense
mx of osmotic pressure
nutriction
acid/base regulation
normal osmotic pressure
25 mmHg
platelet function
hemostasis regulation
infmalattory process
RBC function
O2 delivery
CO2 removate
left shift curve
incr O2 affinity / decr perfusion
decr pCO2
decr H+
decr 2,3 DPG
decr temp
HbF
right shift curve
decr O2 affinity/incr perfusion
incr pCO2
incr H+
incr 2,3 DPG
incr temp
normal P50
26 mmHg
methemoglobinemia
iron is oxidize from Fe2+ to Fe 3+
“functional” anemia
unable to deliver O2 to tissue adquately
dyspnea or cyanosis
85% SpO2
methemoglobinemia curve shift
left shift
meth treatment
MB (1-2 mg/kg)
carboyhemoglobinemia
CO is bound to Hg instead of O2
normal SpO2
cherry red skin
carboxyhemogloin treatment
supplement O2
hyperbaric chamber
sickle cell anemia
substitution on beta subunit
hypoxia
autosomal recessive
hemolytic anemia
what to avoid in sickle cell pts
dehydration
acidosis
hypothermia
tourniquets
when do WBC increase
infections
inflammation
cancer
when do WBC decrease
meds
autoimmune
Hg/Hct increase
smoking
genetic polycythemia
altitude
Hg/Hct decrease
hemodilition
blood loss
low Fe/B12/folate
inherited blood condition
kidney disease
cancer
Plt increase
increased production
Plt decrease
low production
rapid destruction
primary hemostasis
plt activation/adhesion
primary hemostasis is promoted by
vWF
extrinsic patheay
response to external trauma
what is activated in extrinsic
Factor VII –> Factor X
intrinsic pathway
response to internal damage to endothelium
what is activated in intrinsic
Factor XII + Facot XI + Factor IX —> Factor X
vWF stabilized Factor VIII —> Factor X
common pathway
Factor I, II, V, X, XIII
Hgb lab values
12-17.5
Hct
34-52
Plt
150-450
WBC
4.5-11
PT
10-13
PTT
25-35
INR
0.8-1.2
PT/INR measures
extrinsic
PTT measures
intrinsic
ACT
time it takes for whole blood to clot in tube
normal ACT
70-120 seconds
unable to clot (hypocoagulable)
hemophilia
von willibrands
hpocoagulable values
thrombocytopenia
hypothermia
acidosis
anemia
what causes thrombocytopenia
drugs (heparin/NSAIDs)
alcohol
liver failure/cirrhosis
DIC
innapropriate acitivation of clotting cascade
uses up coags
excessive clotting (hypercoagulable)
factor V leiden
antithrombin III
protein C/S def
antphospholipid syndrome
drugs
cancer
pregnancy
DIC labs
decr plt/fibrinogen
incr PT/PTT/INR
incr D dimer
trauma triad aof death
hypothermia
acidosis
coagulopathy
coumadin (warfarin)
extrinsic
PT
warfarin reversal
PCC
vit K
FFP
Heparin
intrinsic
PTT/ACT
heparin reversal
protamine (1 mg/100 units heparin)
antigens are found
on RBC
antibodies are found
in plasma for antigen that they DO NOT HAVE
group A
anti-B antibodies
A antigen
group B
anti-A antibodies
B antigen
Group AB
no antibodies
A and B antigen
Group O
anti- A and anti-B antibodies
no antigens
RH+ can receive
RH+ and Rh-
Rh- can receive
Rh- only
plasm universal recipient
type O
plasma universal donor
type AB
blood universal donor
O-
blood universal receiver
AB+
agglutination
occurs wehn antigen is mixed with corresponding antibody
type and scree
<1% risk
45 mins
type and cross
no risk
1 hr
PRBC volume
250 mL
PRBC Hct
70%
PRBC shelf life
35 days frozen at 1-6 C
PRBC uses
1 unit raises:
Hg 1 g/dL
Hct 3%
PRBC risks
citrate toxicity
hypothermia
hyperkalemia
decr 2,3 DPG
when do you need to consider PRBC transfusion
Hg 6-10 g/dL
Plts volume
50-70 mL
plt storage
20-24C for 5 days
Plts uses
1 unit raises plt by 5-10000/mm3
FFP
plasma proteins/clotting factorts
200-250 mL
plts indictaion
thrombocytopenia
plt dysfunction
is ABO compatibility needed for plts
no
FFP uses
1 unit will raise clotting factor by 2-3%
is abo compatibility neede for FFP
yes but not Rh
FFP indications
tx of isolated factor deficiencies
warfarin reversal
coagulopathy
massive blood loss/transfusion
cryo
precipoitate remaining after ffp is thawed slowly
10-15 mL
F VIII, FXII, vW, fibrinogen
1 unit of cryo
increase fibrinoge 5-7 mg/dL
cryo indiscations
FVII deficiency
hemophilia A
fibrinogen deficiency
which blood products do you heat
RBC
FFP
blood products must be
filtered (170 micron filter)
blood product veriofication before administration
unit #
blood type
expiration date
2 staff members must verify
blood consents
mandatory for every pt
are there any mandatory transfusion triggers
NO
allowable blood loss calculatiuon
ABL = EBV x [(Hct i - Hct f) / Hct i]
EBV premature neonates
95 mL/kg
EBV full term neonates
85 mL/kg
EBV infants
80 mL/kg
EBV adult men
75 mL/kg
EBV adult women
65 mL/kg
EBV morbid obese
55 mL/kg
ermgency transfusion blood type known
abbvreviated cross match
blood type unknown
give O- until correct type and cross is done
MTP
need to transfuse 1-2x pt blood
TRALI
leading cause of deth from transfusion
TRALi occurs within
6 hrs
TRALI is mnore common with
plt
FFP
TRALI symptoms
dyspnea
cyanosis
chills/fever
decr BP
TRALI presentation
acute hypocia
non cardiac pulmonary edema
TRALI treatment
supplemental O2
vent support as needed (low TV, incr RR)
TACO
transfusion associated circulatory overload
TACO occurs when
blood products are administered too quickly
TACO is more common in what pts
cardiac/renal dysfunction
TACO symptoms
respiratory distress
PE
elevated BNP
elevated CVP
TACO occurs within
12 hrs of the transfusion
TACO treatment
stop transfusion
supp O2
ventilatory support
diuresis