PRE-TRANSFUSION TESTING
1-Determination of recipient ABO group.
2-Determination of
recipient Rh (D) type
3-Determination of
recipient serum alloantibodies
4-Crossmatch between patient serum & Donor RBCS
5-Coomb s test: "not routine"
6 - selection of blood product for transfusion:
Packed Rbcs:
*One unit increases Hgb by lgmldl
*Indication: chronic symptmatic anemia
spesially coronaryA.D.
Active
bleeding
*Not used to supply
Plts ,
Adequate blood volume or
coauqulstion factors
Random-donor plt concatenate:
1unit whole blood gives bag of plts contains
70ml plasma
1unit plts increases plts count by 5xl09/L
Indication: 1- proplyact* no bleeding
2-
bleeding
HLA matched plts
-by hemapharesis
- contain 3× 1011 plts
-equal to 6:8 units radorn donor plt conc.
-Used in pt. need plts but refractory
to plts Transfusion
Factor Vlll concentcrate
hemophilia A
factor 1X concentcrate
hemophilia B
hemophilia A wit inhibitors to factor Vlll
congenital decrease of factor Vll and X
Albumin:-
1- Acute
volume expansion
Hyov. Schock
Chronic Albumin depletion
2- long term replacement (burn)
3- Cadiopulm. pypass priming
4- thesapeutic Plasmapharesis.
FFP.
1-multiple coagul. facter (DIC ,Liver disease )
2-Massive transfusion
3-Specific coag. factor deficiency(antithrombin 111, ll, V, Vll)
4-warfarin overdose Adverse
effects of transfusion:.
I mmune mediated adverse effects:-
1-Acute hemolytic transfusion reactions:
*Pathogenesis: transfusion of AB0incompatible whole bl.
or RBcs
*c/p:. pain at tran. site, chest pain, back pain, fever,
chills, nausia ,dyspnea ,oliguria hemoglobinuria, hypotension ,shock, excessive
bleeding
*treatement- Discontinue -Fluid
,diuretic-treatDIC,hypotension&promote Renal blood flow
•
-
treatDIC
•
Investigation: -indirect serum
bilirub.increased
•
-LDH -direct antigloulin test (+)
2-Delayed hemolytic transfusion reaction
Pathogenesis. Immunization against RBS alloantigen
C/P:-
-
Subclincal
-
- unexplained
Hgb decreased
Fever - chills - anemia - Jundice
Hemoglobinuria
treatement: Renal function monitoring
(in Renal diseased patient)
serious sequalae are infrequent.
Investigation:
direct antigloulin test (+)
indirect antigloulin test (+)
3- febrile nonhemlytic transfusion reaction
recipient
develops cytotoxic antibodiesagainst antigens on donor granulocyte, lymphocytes
or platelets (leukoagglutinins).
Ag AB. interaction with
complement activation,
pyrogens release &fever.
Commonly seen in
multitransfused pts.
C / p:
-during or shortly after transfusion.
-Fever
chills or rigors
tretement: -Exclude hemolytic transf. reaction
-discontinue
tran. -
Antipyretic
.
4- Non cardiogenic pulmonary oedama.
Pathogenesis:
Patient lenkoagglutinins leads to Ag – AB
intcraction
and leuckocytes aggregation trarring
in pulmonary
Vasculature&increased
vascular permeability.
C/P: fever ,chills, Acute pul. oedma.
No evidence of lt
ventricular dysfunction.
tretement :
- discontinue
trans.
- Rule out Acute hemolytic tran.
reactions
- I.V. steroids
- Leukocyts free
bl. products.
5- Allergic transfusion reaction
- **Urticarial reactions:
Pathogenesis:
Transfused soluble atopens
(commm in those with history of allrgy),
histamie release from IgE
ore IgG coated mast cells.
C/P. pruritis – usually without fever
treatement . temporary interruption of trans.
Antihistaminics
**Anaphylactic reactions:
- relatively
rare – commm in IGA deficient pts
- may occur
after only small dose transfusion
tretement: stop transf. ,tretement hypoten ,epinephrine
Prevention:- RBcs extensively washed &free
of plasma
- autologous
donor program before elective surgery.
.
6Allo imm unization:
Against alloantigenis compoments in
blood products :
1--- Allo immuniZation to RBcs Antigens:-
(Acute or delayed hlytic
reactions).
2---Allo immuniZation to plts
***(Abs developed against plts associated HLA -Ags leads to
Refractoriness to plts transfusion
typically seen in multitramsfued
pts .
tretement HLA
matched plts.
***Abs againt plts
specific Ags leads to
-Neonatal alloimmune thrombocytopenia
-Post transf. purpura *5: 15 days after transf. *tretement
:
plasma
pharesis &
autologous transfusisn.
7- GVHD
c/p.
Develop: 30days
after transf.
fever liver
dysfunction
diarrhea infections pancytopenia.
tretement:ATG,
steroids,
methothexate.
Cyclosporine, bl. Products irradiation
(2) Infectious diseases
transimission
*Viral:-
-hepatotropic, HCV,HBV,HDV
-Herpes
virus: CMV ,EBV
-Retro
Virus:--- HILV-1
(tropical Spastic Parapares or
Adult T cell
leuk. Lymphoma.
---HIV (AIDS
*Non Viral:
-Syphilis: (treponema pallidum)
-Brucellosis (brucella species)
-gram – ve bact. Contamination (Yersinia &E-coli)
-Malaria
-Chagas' disease (trypanosoma cruzi)
-Toxoplamosis (toxoplasma gondii)
-Babesiosis (babesia microti)
-Syphilis: (treponema pallidum)
-Brucellosis (brucella species)
-gram – ve bact. Contamination (Yersinia &E-coli)
-Malaria
-Chagas' disease (trypanosoma cruzi)
-Toxoplamosis (toxoplasma gondii)
-Babesiosis (babesia microti)
(3) Complications related to massive transfusion.
-Replacement of pt bl. Volume by stored bl. In less than 24 h.
-Necessary in trama, liver transplant, vascular surgery.
1- hemostatic abnormalities.
Dilution plts & coag. Factors in circulation. → DIC
tretement- replacement Of coag. factors &plts.
2- citrate toxicuty:
Hypocalcemia → cardiac dysfunction.
tretement: calcium
3- hypothermia:
Massive tr. Of stored refrigerated bl.
→ candiac dysrrhythmia.
tretement– use warmer blood.
4- K imbalance:
---Hypokalemia
If metabolic Alkalosis
due to citsate.
---Hyperkalemia.
Due to ↑ plts & plasma k with storage.
(uncommon)
5- Acid base imbalance:
Early → metabolic acidosis
Late → metabolic alkalasis
6. mechanical trauma to
BBs: → hemolysis.
(4) other Non
immunologic complications
1- circulatory overload:
In carliopulmanary compromised pts.
C/p: dyspnea ,
cyanosis ,
penipheral oedema.
tretement:
discontinue,
tretement overload,
Slow
infusion of single component
2- hemosiderosis:
1unit RBCS → contain 200 mg iron.
Chronic Transf. → cardiac,
endocrine&
hepatic dysfunction.
tretement: iron chelating agents.
Alternatives to homologous blood
Transfusion
(1) Autologous blood Transfusion:
Is: any bl. Component donated by intended recipient.
Benefits: (low risk of):
Alloimmunlzation
GVHD
Infections dis.
transmission.
Febrile, hlytic,
allergic reaction.
Categories:
(1) autologus whole bl. Or KBcs.
* preoperative donation:
- before elective surgery (anticipated bl. loss)
- contraindication:
-
symptomatic angina, AS, Valvular HD.
-
recent seizures.
-
hematocrit ↓ 33%
* Intraoperative
hemodilution:
- in cardiopulmonary bypass procedure.
-
1 or 2 units of bl. Removed →
-
replaced by colloid or crystalloid
-
→ after surgery →
-
transf. of autol. b1ood& diuretics
-
(to ↓ plasma volume).
-
* post operative blood. salvage
-
Significant drainage form cavity as
-
chest cavity drainge ,,
-
collect blood during 24: 48 h postoerative →
-
Filteration →
-
reisfuse within 6h of
collection
-
(2) Autologous plts transfusion.
-
Preoperative Collection by hemapharis
-
→ frozen for future use
-
as anticipation of BM suppression during chemotherapy.
-
(3) autologous FFP or csuopercipitate.
-
Very uncommon indication.
-
(4) autologus concenterated fibrinogn.
-
Separated from autologus plasma.
-
(2) Growth factors
-
Epo: ↑ RBs production& ↓ need RBs donation
-
GM- CSF or G – csf:
-
stimulate hematopoiesis
-
used with BMT&chemotherapy.
-
(3) blood substitutes
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