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Transcript
Administration of Blood and
Blood Component
Dr.Azarm
Blood Products
‫روشهاي صحيح مصرف خون‬
‫به منظور كاهش‬
‫ترانسفوزيونهاي غير‬
‫ضروري‬
‫‪Dr.Azarm‬‬
‫چرا الزم است خون وفراوردههاي خوني‬
‫صحيح و هدفمند مصرف شوند؟‬
‫‪-----------------------------------‬‬‫‪-1‬خون ساختني نيست بلكه بايد اهدا‬
‫شود‪.‬‬
‫‪-2‬در همه جا خون فراوري نمي شود و در دسترس‬
‫نمي باشد‪.‬‬
‫‪-3‬هميشه اهدا كننده اماده وجود‬
‫ندارد‪.‬‬
‫‪-4‬عوارض انتقال خون هميشه بايد مد نظر‬
‫باشد‪.‬‬
‫‪Dr.Azarm‬‬
‫نكات مهم‬
‫• خون و فرآوردههاي خون بايد در اسرع وقت تزريق شود‪.‬‬
‫• چنانچه فرآوردهاي براي ‪ 30‬دقيقه يا بيشتر در دماي‬
‫اتاق قرار گيرد نبايد تزريق شود‪.‬‬
‫• خون و فرآوردههاي خون نبايد در داخل يخچال اتاق‬
‫پرستاري ذخيره شود مگر در مواقع خاص مانند‬
‫اتاق عمل يا در اتاق ‪.recovery‬‬
‫• چنانچه به هر علت واحد خون)‪ (RBC‬باز نشود و‬
‫در دماي مناسب قرار داشته باشد و در فاصله زماني‬
‫كمتر از ‪ 30‬دقيقه‪ ،‬به بانك خون برگردد ميتوان از‬
‫آن استفاده كرد‪.‬‬
‫نكات مهم‬
‫• خون نبايد در داخل ظرف حاوي آب داغ قرار گيرد‬
‫زيرا اين عمل باعث هموليز گويچههاي سرخ و آزاد‬
‫شدن پتاسيم از گويچههاي سرخ ميشود كه ميتواند‬
‫براي زندگي بيمار مخاطرهآميز باشد‪.‬‬
‫• فرآوردهاي كه ذوب شده نبايد دوباره منجمد شود و‬
‫بايد هرچه زودتر مصرف شود‪ .‬در صورتي كه به‬
‫هر دليل تاخيري در تزريق رخ دهد‪ ،‬بايد در دماي‬
‫محيط نگهداري شده و در عرض ‪ 4‬ساعت مصرف‬
‫شود‪.‬‬
‫• توجه‪ :‬مهمترين مرحله نظارت‪ 15 ،‬دقيقه اول تزريق‬
‫ميباشد‪.‬‬
Whole Blood
Dr.Azarm
Whole Blood
Description:
•
•
•
•
•
•
•
Up to 510 ml total volume
450 ml donor blood
63 ml anticoagulant-preservative solution
Haemoglobin approximately 12 g/ml
Haematocrit 35%–45%
No functional platelets
No labile coagulation factors (V and VIII)
Infection risk
Not sterilized, so capable of transmitting any
agent present in cells or plasma which has
not been detected by routine screening for
transfusion-transmissible
infections, including:
HIV-1 and HIV-2, hepatitis B and C,
other hepatitis viruses, syphilis, malaria and
Chagas
Storage
• Between +2°C and +6°C in approved blood
bank refrigerator, fitted with a temperature chart
and alarm
• During storage at +2°C and +6°C, changes in
composition occur resulting from red cell
metabolism
• Transfusion should be started within 30
minutes of removal from refrigerator
Indications
• Red cell replacement in acute
blood loss with hypovolaemia
• Exchange transfusion
• Patients needing red cell
transfusions where red cell concentrates
or suspensions are not available
Contraindications
Risk of volume overload in
patients with:
• Chronic anaemia
• Incipient cardiac failure
Administration
• Must be ABO and RhD
compatible with the recipient
• Never add medication to a unit
of blood
• Complete transfusion within 4
hours of commencement
RED CELL CONCENTRATE
(‘Packed red cells’, ‘plasma-reduced blood’)
Description
• 150–200 ml red cells from which most of the
plasma has been removed
• Haemoglobin approximately 20 g/100 ml
• Haematocrit 55%–75%
Infection risk
• Same as whole blood
Storage
• Same as whole blood
Indications
• Replacement of red cells in
anaemic patients
• Use with crystalloid
replacement fluids or colloid
solution in acute blood loss
‫مواردي كه نياز به تزريق وجود ندارد‬
‫•‬
‫•‬
‫•‬
‫•‬
‫•‬
‫•‬
‫•‬
‫•‬
‫‪ :A‬آنمي همراه با كمبود آهن‬
‫‪ :B‬آنمي پرنيسيوز‬
‫‪ :C‬كمبود تغذيهاي‬
‫‪ :D‬عدم جذب گوارشي‬
‫‪ : E‬ترميم زخم‬
‫‪ :F‬كمبود فوالت و ‪B12‬‬
‫‪ :G‬آنمي همولتيك ارثي‬
‫‪ :H‬براي بهبود حال عمومي‬
‫فقط هنگامي كه خونريزي فعال از دستگاه گوارش يا جاي ديگر بدن باشد نياز‬
‫به تزريق داريم البته در چنين بيماراني هدف تصحيح هموگلوبين نيست بلكه‬
‫هموگلوبين در حدي باشد كه بيمار عالئم حياتي پايدار داشته باشد‪.‬‬
‫نوزادان و كودكان ‪:‬‬
‫در بيماران با سن كمتر از ‪ 4‬ماه‬
‫هموگلوبين كمتر از ‪ 13‬گرم در دسيليتر همراه با بيماريهاي شديد‬
‫و سيانوتيك قلب و ريه و يا نارسايي قلب هموگلوبين كمتر از ‪10‬گرم‬
‫در دسيليتر همراه با بيماريهاي ريوي متوسط‬
‫از دست رفتن سريع و حاد بيش از ‪ %10‬حجم خون‬
‫هموگلوبين كمتر از ‪ 8‬گرم در دسي ليتر همراه با آنمي عالمتدار‬
‫اين راهنماها يك پيشنهاد ميباشد و بايستي در مورد هر نوزاد به *‬
‫تنهايي تصميم گيري كرد‪.‬‬
‫در هموگلوبين كمتر از ‪ 10‬گرم در دسيليتر كه كانديد عمل جراحي‬
‫بزرگ هستند‪.‬‬
‫•‬
‫•‬
‫•‬
‫•‬
‫دركودكان با سن بيشتراز‪ 4‬ماه‬
‫هموگلوبين قبل از عمل جراحي كمتر از ‪ 8‬گرم در‬
‫دسيليتر و يا هماتوكريت زير ‪ %25‬و يا هموگلوبين زير‬
‫‪ 8‬گرم در دسيليتر بعد از عمل كه همراه با عاليم و‬
‫نشانههاي كم خوني باشد‪.‬‬
‫كاهش و يا از دست رفتن سريع و حاد بيش از ‪ %15‬حجم‬
‫خون يا وجود عاليم و نشانههاي هيپوولمي كه به تزريق‬
‫مايعات كريستالوئيد يا كلوئيدي پاسخ نداده باشد‪.‬‬
‫هموگلوبين كمتر از ‪13‬گرم در دسيليتر در بيماري شديد‬
‫قلبي ريوي (سيانوز‪-‬دسترين تنفسي)‬
‫هموگلوبين كمتر از ‪ 8‬گرم در دسيليتر در ‪:‬‬
‫•‬
‫•‬
‫•‬
‫•‬
‫•‬
‫هموگلوبين كمتر از ‪ 8‬گرم در دسيليتر در ‪:‬‬
‫الف) بيماراني كه تحت شيميدرماني يا راديوتراپي هستند‪.‬‬
‫(نارسايي مغز استخوان)‬
‫ب ) بيماراني كه دچار كمخوني مزمن هستند كه به درمان طبي‬
‫پاسخ ندادهاند يا عاليم و نشانههاي كم خوني دارند‪.‬‬
‫عوارض بيماري سيكلسل نظير حوادث عروقي مغزي‪Acute ،‬‬
‫‪ chest syndrom‬و آمادگي براي عمل جراحي‪.‬‬
‫در بيماران بتاتاالسمي هموزيگوت و يا هتروزيگوت كه بيشتر از‬
‫ساير انواع تاالسمي دچار آنمي شديد ميشوند براي جلوگيري از‬
‫عوارضي مانند رشد نابهنجار استخوان و بهبود در سرعت رشد‬
‫و كاهش بار آهن بهتر است هموگلوبين در محدودة ‪ 10‬گرم در‬
‫دسيليتر كنترل شود‪ .‬البته قبل از تزريق نبايد هموگلوبين بيشتر‬
‫از ‪ 5/9‬گرم در دسيليتر باشد تا از افزايش بار آهن جلوگيري‬
‫شود‪.‬‬
Administration
• Same as whole blood
• To improve transfusion flow,
normal saline (50–100 ml)
may be added using a Ypattern infusion set
RED CELL SUSPENSION
Description
• 150–200 ml red cells with minimal
residual plasma to which ±100 ml normal
saline, adenine, glucose,mannitol
solution (SAGM) or an equivalent red cell
nutrient solution has been added
• Haemoglobin approximately 15 g/100 ml
• Haematocrit 50%–70%
•
•
•
•
Infection: risk Same as whole blood
Storage: Same as whole blood
Indications: Same as red cell concentrate
Contraindications: Not advised for
exchange transfusion of neonates. The
additive solution may be replaced with
plasma, 45% albumin or an isotonic
crystalloid solution, such as normal
saline
• Administration : Same as whole
blood
• Better flow rates are achieved than with
red cell concentrate or whole blood
Frozen RBCs
• Add cryoprotectant glycerol to RBCs followed by
appropriate freezing (-65°C or lower) allows storage of
RBCs for 10 years.
• When Cells needed, unit thawed and washed with
saline to remove glycerol. Washing “enters” storage
bag-unit can be stored for only 24 hours at 1° to 6°C
after thawing.
• Used primarily to maintain supplies of uncommon RBC
phenotypes needed by patients with alloantibodies
against frequently occurring RBC antigens
• Military uses to maintain emergent blood supplies.
Leukocyte Poor RBCs
Leukocyte-Reduced Red Blood Cells
Description
• A red cell suspension or concentrate containing
<5 x 106 white cells per pack, prepared by
filtration through a leucocyte-depleting filter
• Haemoglobin concentration and haematocrit
depend on whether the product is whole blood,
red cell concentrate or red cell suspension
• Leucocyte depletion significantly reduces the
risk of transmission of cytomegalovirus (CMV)
Indications
• Minimizes white cell immunization in patients
receiving repeated transfusions but, to achieve
this, all blood components given to the patient
must be leucocyte-depleted
• Reduces risk of CMV transmission in special
situations
• Patients who have experienced two or more
previous febrile reactions to red cell transfusion
Contraindications
• Will not prevent graft-vs-host disease:
for this purpose, blood components should be
irradiated where facilities are available
(radiation dose: 25–30 Gy)
Administration
• Same as whole blood
• A leucocyte filter may also be used at the time
of transfusion if leucocyte-depleted red cells or
whole blood are not available
Washed RBCs
• Washed RBCS are RBCs washed with saline to
remove most of the plasma.
• Washed RBCs are not leukoreduced.
• Indications-patients who have had severe allergic
reactions associated with transfusion or
immunoglobulin A (IgA) deficiency.
• Washed RBCs must be given through a standard
blood filter, can transmit hepatitis and other
infectious diseases
• Because bag must be entered to introduce saline,
washed RBCs must be given within 24 hrs of
preparation.
Irradiated WB or RBCs
• Blood components exposed to standard dose of
ionizing radiation to make viable lymphocytes
unable to engraft (to reduce GvH) in premature
newborns or highly immunocompromised patients
(e.g., bone marrow or solid organ transplant).
• “Although no significant adverse red cell
structural events have been noted, mild functional
impairment manifested by significant leakage of
potassium and accumulation of plasma hgb has
been noted after gamma irradiation.”
•
ASA Questions and Answers About Transfusion Practice- 2002
‫گرم كردن خون‬
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‫•‬
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‫در مواردي كه يك حجم خون و يا بيشتر طي ‪ 24‬ساعت جايگزين شود‪ ،‬تزريق خون‬
‫را ماسيو مينامند‪ .‬يك حجم خون به ميزان ‪ ml/Kg 75‬يا حدود ‪ ml 5000‬تخمين‬
‫زده ميشود‪.‬‬
‫‪ Exchange Transfusion‬نوزادان‬
‫در صورتي كه بيمار داراي ‪Ab‬هاي واكنشدهنده در دماي سرد)‪(Cold Antibody‬‬
‫باشد‪.‬‬
‫زماني كه بيمار آريتمي داشته باشد‪.‬‬
‫براي زماني كه خون با سرعت ‪ ml/minute50‬براي ‪ 30‬دقيقه يا بيشتر براي‬
‫‪ ml/Kg/hour15‬براي كودكان تنظيم شده باشد‪.‬‬
‫بزرگساالن و سرعت‬
‫براي بيماران در طول عمل جراحي ‪ Bypass‬در فاز ‪re-warming‬‬
‫پالسمافرزيس درماني يا فرآيند ‪Red cell exchange‬‬
‫تزريق خون در نوزادان و كودكان‬
‫سندرم رينود يا وازواكتيو ناشي از سرما‬
Use of RBCs in Massive
Transfusion
• If 50-75% blood volume replaced by type
0 Blood (10 U RBCS in adult)• May need to continue with type 0 blood• “Otherwise, risk of major cross-match
reaction increases.
• Patient may have received enough anti-A
or anti-B antibodies to precipitate
hemolysis if A,B, or AB units
subsequently given”
•
Smith, C.(2003)Current Practices in Fluid and Component Therapy ITACCS. Seminar-Massive
Transfusion
Massive Transfusion
 Give
blood products as a ratio
 1 dose : 1 dose : 1 dose
: 1 dose
5
RBC : 2 FFP : 6 RD PLT : 10 Cryo
 ________________ (1 PPH) _________
 Hgb
PT PTT Plt Ct
Fib
FFP
Description
• Pack containing the plasma separated from one
whole blood donation within 6 hours of
collection and then rapidly frozen to –25°C or
colder
• Contains normal plasma levels of stable clotting
factors, albumin and immunoglobulin
• Factor VIII level at least 70% of normal fresh
plasma level
FFP
• Collected by centrifugation of whole blood, or by
apheresis as a single donor unit (taken for plasma,
or as a by product of RBC or platelet apheresis)
• Must be frozen within 6 hours of collection,can be
kept frozen for a year, takes 20-30 minutes to
thaw,
• Before use, should be thawed in the blood bank in
water which is between 30°C to 37°C. Higher
temperatures will destroy clotting factors and
proteins
• is then kept at 1-6° and transfused within 24 hours
FFP
• Need ABO Compatibility, but Rh Neg
patients can receive Rh Pos FFP
• 4-5 Units of platelets, one unit WB all
have same a similar quantity of
coagulation factors as unit of FFP
(except for labile factors lost to cold
storage in WB)
Indications
• Replacement of multiple coagulation factor
deficiencies: e.g.
—Liver disease
—Warfarin (anticoagulant) overdose
—Depletion of coagulation factors in patients
receiving large volume transfusions
• Disseminated intravascular coagulation (DIC)
• Thrombotic thrombocytopenic purpura (TTP)
Precautions
• Acute allergic reactions are not uncommon,
especially with rapid infusions
• Severe life-threatening anaphylactic reactions
occasionally occur
• Hypovolaemia alone is not an indication for use
FFP
• Goal- to raise level of clotting factor to 30% of
normal
• Takes 10-15 cc/kg
• Rapid reversal of coumadin 5-8cc/kg FFP
(Vitamin K would take 12-18 hours)
•
Clin Anes Procedures-Mass Gen-2002
Cryoprecipitate
Description
• Prepared from fresh frozen plasma by collecting
the precipitate formed during controlled thawing
at +4°C and resuspending it in 10–20 ml
plasma
• Contains about half of the Factor VIII and
fibrinogen in the donated whole blood: e.g.
Factor VIII: 80–100 iu/pack; fibrinogen: 150–
300 mg/pack; factor XIII: 40 to 60 U/pack
Cryoprecipitate
• Shelf life-Frozen: 1 yr (<–30°C)
Thawed: Give within 6 hours
• Preferable to be ABO compatible (AABB) May
have RBC fragments that can sensitize Rh-D
neg patients
Indications
• As an alternative to Factor VIII concentrate in
the treatment of inherited deficiencies of:
— von Willebrand Factor (von Willebrand’s
disease)
— Factor VIII (haemophilia A)
— Factor XIII
• As a source of fibrinogen in acquired
coagulopathies: e.g. disseminated intravascular
coagulation
Cryoprecipitate
• A dose of 1 unit (bag) of cryoprecipitate per 710 kg body weight raises fibrinogen levels by
at least 50 mg/dL.
• The half-life of fibrinogen is 3 to 5 days;
additional doses given on the basis of lab test
results.
Platelets
Description
Single donor unit in a volume of 50–60 ml of
plasma should contain:
• At least 55 x 109 platelets
• <1.2 x 109 red cells
• <0.12 x 109 leucocytes
Unit of issue
May be supplied as either:
• Single donor unit: platelets prepared from one
donation
• Pooled unit: platelets prepared from 4 to 6
donor units ‘pooled’ into one pack to contain an
adult dose of at least 240 x 109 platelets
Infection risk
• Same as whole blood, but a normal adult dose
involves between 4 and 6 donor exposures
• Bacterial contamination affects about 1% of
pooled units
Storage
• Up to 72 hours at 20°C to 24°C (with agitation)
unless collected in specialized platelet packs
validated for longer storage periods; do not
store at 2°C to 6°C
• Longer storage increases the risk of bacterial
proliferation and septicaemia in the recipient
Indications
• Treatment of bleeding due to:
— Thrombocytopenia
— Platelet function defects
• Prevention of bleeding due to
thrombocytopenia, such as in bone marrow
failure
‫•‬
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‫•‬
‫•‬
‫•‬
‫در صورتي كه تعداد پالكتهاي بيمار كمتر از ‪ 000/10‬در ميكروليتر يا‬
‫كمتر از ‪ 000/20‬در ميكروليتر و همراه با تب باشد‪.‬‬
‫مواردي كه توليد پالكت در مغز استخوان كاهش يافته باشد و يا بين‬
‫‪ 000/10 -000/20‬در ميكروليتر باشد مانند بيماران داراي‬
‫بدخيميهاي خوني و يا بيماراني كه تحت كموتراپي بودهاند‪.‬‬
‫شمارش پالكت كمتر از ‪ 000/50‬در ميكروليتر براي جراحيهاي كوچك‪.‬‬
‫شمارش پالكت كمتر از ‪ 000/80‬در ميكروليتر براي جراحيهاي بزرگ‪.‬‬
‫شمارش پالكت كمتر از ‪ 000/50‬در ميكروليتر در بيماراني كه‬
‫خونريزي فعال دارند‪.‬‬
‫شمارش پالكت كمتر از ‪ 000/50‬در ميكروليتر در بيماراني كه تحت‬
‫ترانسفوزيون وسيع قرار داشتهاند‪.‬‬
‫شمارش پالكت كمتر از ‪ 000/50‬در ميكروليتر در بيماراني كه قرار‬
‫است مورد اعمال تهاجمي قرار ميگيرند‪.‬‬
‫•‬
‫•‬
‫•‬
‫•‬
‫•‬
‫•‬
‫شمارش پالكت كمتر از ‪ 000/100‬در ميكروليتردر بيماران كه‬
‫داراي يكي از خصوصيات زير‪:‬‬
‫‪ :a‬خونريزي رتين‬
‫‪ :b‬خونريزي مغز‬
‫‪ :c‬افراد تحت جراحي باي پاس)‪ (By-Pass‬كه دچار‬
‫خونريزي شدهاند‪.‬‬
‫با زمان سيالن بيش از ‪ 5/7‬دقيقه با شمارش پالكت طبيعي‪،‬‬
‫خونريزي يا اعمال جراحي تهاجمي در بيماران دچار اختالل كيفي‬
‫پالكت‬
‫در درمان لوكمي حاد براي جلوگيري از مرحله خونريزي وسيع‬
‫(‪ )Episode Major Bleeding‬به جز فاز انتهايي‬
Platelet Transfusion:
Response evaluation to plt transfusion:
Corrected Count Increment:
( CCI)
CCI= Plt increment multiply BSA/ Number of plt transfused
Platelet Transfusion:
Response Evaluation:
CCI must be at least 7500 one hour and
4500 ,20 hours after transfusion.
So if it doesn’t occur we can say that patient
has platelet resistance.
Contraindications
• Not generally indicated for prophylaxis of bleeding in
surgical patients, unless known to have significant preoperative platelet deficiency
• Not indicated in:
— Idiopathic autoimmune thrombocytopenic purpura
(ITP)
—Thrombotic thrombocytopenic purpura (TTP)
— Untreated disseminated intravascular coagulation
(DIC)
— Thrombocytopenia associated with septicaemia,
until treatment has commenced or in cases of
hypersplenism
Dosage
• 1 unit of platelet concentrate/10 kg body weight:
in a 60 or 70 kg adult, 4–6 single donor units
containing at least 240 x 109 platelets should
raise the platelet count by 20–40 x 109/L
• Increment will be less if there is:
— Splenomegaly
— Disseminated intravascular coagulation
— Septicaemia
Administration
• After pooling, platelet concentrates should be infused as
soon as possible, generally within 4 hours, because of the
risk of bacterial proliferation
• Must not be refrigerated before infusion as this reduces
platelet function
• 4–6 units of platelet concentrates (which may be supplied
pooled) should be infused through a fresh standard blood
administration set
• Special platelet infusion sets are not required
• Should be infused over a period of about 30 minutes
• Do not give platelet concentrates prepared from RhD
positive donors to an RhD negative female with
childbearing potential
• Give platelet concentrates that are ABO compatible,
whenever possible
Complications
• Febrile non-haemolytic and allergic
urticarial reactions are not uncommon,
especially in patients receiving multiple
transfusions
PLATELET CONCENTRATES
(collected by plateletpheresis)
Description
• Volume 150–300 ml
• Platelet content 150–500 x 109, equivalent to 3–10
single donations
• Platelet content, volume of plasma and leucocyte
contamination depend on the collection procedure
Unit of issue
• 1 pack containing platelet concentrates collected
by a cell separator device from a single donor
Infection risk
Same as whole blood
Storage
• Up to 72 hours at 20°C to 24°C (with agitation)
unless collected in specialized platelet packs
validated for longer storage periods; do not
store at 2°C to 6°C
Indications
• Generally equivalent to the same dose of platelet
concentrates prepared from whole blood
• If a specially typed, compatible donor is required for
the patient, several doses may be obtained from the
selected donor
Dosage
• 1 pack of platelet concentrate collected from a single
donor by apheresis is usually equivalent to 1
therapeutic dose
Administration
• Same as recovered donor platelets, but ABO
compatibility is more important: high titre anti-A
or anti-B in the donor plasma used to suspend
the platelets may cause haemolysis of the
recipient’s red cells
That’s all, folks!