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Blood Bank QEH- An era of 
bankruptcy??
The rational use of 
blood and blood 
products
Presentation Aims 
 To discuss the following: 
 The various components available from blood 
 The rational use of blood and its components 
 Problems faced by QEH 
 Proposals for improved blood product usage in 
QEH
Blood is an amazing fluid! 
Keeps us warm 
Provides nutrients for cells, tissues and 
organs 
Removes waste products from various sites
What is blood? 
A highly specialised circulating tissue which 
has several types of cells suspended in a 
liquid medium called plasma. 
Origins from Greek ‘haima’ 
Blood is a life sustaining fluid
Blood components 
Packed red cells 
Platelets 
Fresh Frozen Plasma 
Frozen plasma 
Cryoprecipitate 
Albumin 
Immunoglobulins
Local study 
Looked at the donations over period 
January 1, 2006 to December 31, 2006 
Examined the various products collected 
during that period 
Study limitations
Blood groups by month 
200 
180 
160 
140 
120 
100 
80 
60 
40 
20 
0 
Number of 
units 
January May September 
Month 
O+ 
O-A+ 
A-B+ 
B-AB+ 
AB-
Table of ABO and Rh distribution by nation 
ABO and Rh blood type distribution by nation (averages for each population) 
Population O+ A+ B+ AB+ O− A− B− AB− 
Australia[11] 40% 31% 8% 2% 9% 7% 2% 1% 
Canada[12] 39% 36% 7.6% 2.5% 7% 6% 1.4% 0.5% 
Denmark[13] 35% 37% 8% 4% 6% 7% 2% 1% 
Finland[14] 27% 38% 15% 7% 4% 6% 2% 1% 
France[15] 36% 37% 9% 3% 6% 7% 1% 1% 
Hong Kong, China[16] 40% 26% 27% 7% <0.3% <0.3% <0.3% <0.3% 
Korea, South[17] 27.4% 34.4% 26.8% 11.2% 0.1% 0.1% 0.1% 0.05% 
Poland[18] 31% 32% 15% 7% 6% 6% 2% 1% 
Sweden[19] 32% 37% 10% 5% 6% 7% 2% 1% 
UK[20] 37% 35% 8% 3% 7% 7% 2% 1% 
USA[21] 38% 34% 9% 3% 7% 6% 2% 1%
Blood donors 2006 
400 
350 
300 
250 
200 
150 
100 
50 
0 
March 
January 
February 
June 
April 
May 
July 
August 
September 
October 
November 
December 
Month 
Number of units 
reg 
vol 
auto 
dir 
os 
mc
Total Donations 
1 
2 
3 
4 
5 
6
Theoretical Yield of components 
 1 unit of blood theoretically gives 
1 unit FFP 
1 unit PRBC’s 
1 single donor unit cryoprecipitate, single donor unit 
platelets 
Plasma for Ig and albumin 
 In theory 
4138 U of FFP, 4138 U PRBC’s, 4138 U cryo 4138 
single donor units platelets 
 In reality 
334 U FFP, 2405 U PRBC’s, 46U cryo* 
216 U plasma, 409 U platelets*
Component use by month 
200 
180 
160 
140 
120 
100 
80 
60 
40 
20 
0 
Number of 
units 
FFP use by Month 
January June November 
Month 
Surgery 
O&G 
Paeds 
A&E 
Medicine
40 
35 
30 
25 
20 
15 
10 
5 
0 
Number of 
units 
Plasma use by month 
January May September Total 
Month 
Surgery 
O&G 
Paeds 
A&E 
Medicine
Platelet use by month 
40 
35 
30 
25 
20 
15 
10 
0 5 
March 
January 
February 
June 
April 
May 
July 
August 
September 
October 
November 
December 
Month 
Number of SD units 
Surgery 
O&G 
Paeds 
A&E 
Medicine
Discarded Units 
Whole blood 504 (39%) 
Packed cells 13 (5%) 
FFP 29 (9%) 
Platelets 169 (41%)
Blood separation
The Donation Process 
Education 
Recruitment 
Selection 
Donation
Blood Collecting
Blood Donation
Infectious Disease Testing 
 HIV 
 Hepatitis B 
 Hepatitis C 
 HTLV-I and II 
 CMV 
 Malaria 
 Syphilis*
Whole Blood 
It is now used rarely in current practice in 
the UK or U.S.A, although in many countries 
it accounts for most transfusions. 
Almost all whole blood donations are 
processed to separate red cells, platelets 
and plasma.
Whole Blood 
Currently whole blood should only be 
considered in the following scenario: 
An adult has bled acutely and massively 
The adult has already received 5 to 7 units of 
RBC plus crystalloids
Packed red cells 
150-200 mls. of red cells with plasma 
removed 
 Haemoglobin 20g/ 100 ml, PCV 55-75 
Expected rise in Hb with 1 unit of red cells is 
approximately 1g/dL
Indications for Packed Cells 
Massive blood loss 
Anaemia of chronic disease 
Haemoglobinopathies 
Perioperative period to maintain Hb> 7g/dL 
No need for transfusion with Hb >10
Platelets 
150-400 x109 /L 
Platelet units can be either 
Single donor units 
Apheresis units 
1 single donor unit contains 55 x109 
1 apheresis unit contains 240x109
Platelets 
Stored at room temperature 
Constantly agitated 
Only last for 5 days 
1 dose of platelets should raise patient’s 
counts by 30 x109 after 1 hour 
Infused in 15 mins
Indications for platelet transfusion 
BLEEDING due to thrombocytopaenia 
Due to platelet dysfunction 
Prevention of spontaneous bleeding with 
counts < 20
Recommended counts to avoid bleeding 
Platelet 
count /ul 
Clinical Condition 
> 100 000 Major abdominal, chest or 
neurosurgery 
> 50 000 Trauma, major surgery 
> 30 000 Minor surgical procedures 
> 20 000 Prevention/treatment of bleeding in pts 
with sepsis, leukemia, malignancy 
> 10 000 Uncomplicated malignancy, leukemia 
> 5 000 ITP patients at low risk
FFP 
Fresh Frozen Plasma 
Plasma collected from single donor units or 
by apheresis 
Frozen within 8 hours of collection 
-18o to -30o C 
Can last for a year
FFP 
1 unit is 250 ml 
Contains all plasma proteins 
Indications: 
Correction of bleeding due to excess warfarin, 
Vitamin K deficiency, liver disease 
DIC, dilutional coagulopathy 
Inherited factor XI deficiency 
TTP
FFP 
Dose: 15 mls/kg about 3-5 units 
FFP and INR <2 
Give at 1ml/kg per hour in likely fluid 
overload patients 
Given within 24 hours of thawing 
Requesting FFP
Frozen Plasma 
Plasma frozen within 24 hours of collection 
Maintains level of plasma proteins except 
factor VIII 
Same indications as FFP
Cryoprecipitate 
FFP thawed at 4oC and centrifuged 
Cryoprecipitate is the by-product 
Contains Fibrinogen, Factor VIII, Factor XIII, 
von Willebrand’s Factor
Cryoprecipitate 
No longer indicated for Hemophilia* 
Source of Fibrinogen in acquired 
coagulopathies as in DIC; platelet 
dysfunction in uremia 
Indicated for bleeding in vWD, Factor XIII 
deficiency
Cryoprecipitate 
Infused as quickly as possible 
Give within 6 hours of thawing 
10-15 mls; usually 10 units pooled 
10 bags contain approx. 2gm of fibrinogen 
and should raise fibrinogen level to 70mg/dL
Almost there!!!!!!!
Appropriateness of transfusion 
May be life-saving 
May have acute or delayed complications 
Puts patient at risk unnecessarily 
‘ The transfusion of safe blood products 
to treat any condition leading to 
significant morbidity or mortality, that 
cannot be managed by any other means’.
Inappropriateness of transfusion 
Giving blood products for conditions that 
can otherwise be treated e.g. anaemia 
Using blood products when other fluids work 
just as well 
 Blood is often unnecessarily given to raise 
a patient’s haemoglobin level before 
surgery or to allow earlier discharge from 
hospital. These are rarely valid reasons for 
transfusion.
Inappropriateness of Transfusion 
Patients’ transfusion requirements can often 
be minimized by good anaesthetic and 
surgical management. 
Blood not needed exposes patient 
unnecessarily 
Blood is an expensive, scarce resource. 
Unnecessary transfusions may cause a 
shortage of blood products for patients in 
real need.
Problems faced by QEH 
Too few donors 
Lack of equipment 
Insufficient products 
Insufficient reagent 
Infectious disease testing
Recommendations 
 Increase public awareness about need for blood 
and hence the number of voluntary donors 
 Continue to encourage relatives to donate for 
patients* 
 Increase the number of mobile clinics 
 Extend the opening hours for blood collecting
Recommendations 
 Management of stocks of blood and blood 
products 
 Maintenance and replacement of equipment 
 On-going training of Haematology Lab Staff 
 Better management of reagents for- infectious 
disease testing, antigens etc. 
 Improved record keeping 
 Move to electronic record keeping
Recommendations 
View to reduce the need for allogeneic 
transfusions 
Autologous transfusions 
Blood saving devices in OR 
Acute normovolemic haemodilution 
Oxygen carrying compounds
Conclusion 
‘Primum-non-nocere’ 
Weigh risks and benefits 
Haemoglobin level is not the sole indicator 
for transfusion 
Use of appropriate products for the various 
conditions 
Personal ethics
Credits 
Blood bank staff 
Blood collecting staff 
Dr. T. Laurent 
Prof. P. Prussia 
Ms. Kay Bryan
Bibliography 
 Uptodate.com 
 British Transfusion guidelines 2007 
 Clinical use of blood, WHO 
 MJA: Tuckfield et al.,Reduction of inappropriate use of blood products 
by prospective monitoring of blood forms 
 Transfusion practice: Palo et al., Population based audit of fresh frozen 
plasma transfusion practices 
 Vox Sanguinis: Titlestead et al., Monitoring transfusion practices at two 
university hospitals 
 Transfusion: Schramm et al., Influencing blood usage in Germany 
 Transfusion: Healy et al., Effect of Fresh Frozen Plasma on 
Prothrombin Time in patients with mild coagulation abnormalities 
 Transfusion: Sullivan et al., Blood collection and transfusion in the USA 
in 2001 
 Transfusion: Triulzi, The art of plasma transfusion therapy
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Blood bank

  • 1. Blood Bank QEH- An era of bankruptcy??
  • 2. The rational use of blood and blood products
  • 3. Presentation Aims  To discuss the following:  The various components available from blood  The rational use of blood and its components  Problems faced by QEH  Proposals for improved blood product usage in QEH
  • 4. Blood is an amazing fluid! Keeps us warm Provides nutrients for cells, tissues and organs Removes waste products from various sites
  • 5. What is blood? A highly specialised circulating tissue which has several types of cells suspended in a liquid medium called plasma. Origins from Greek ‘haima’ Blood is a life sustaining fluid
  • 6.
  • 7. Blood components Packed red cells Platelets Fresh Frozen Plasma Frozen plasma Cryoprecipitate Albumin Immunoglobulins
  • 8. Local study Looked at the donations over period January 1, 2006 to December 31, 2006 Examined the various products collected during that period Study limitations
  • 9. Blood groups by month 200 180 160 140 120 100 80 60 40 20 0 Number of units January May September Month O+ O-A+ A-B+ B-AB+ AB-
  • 10. Table of ABO and Rh distribution by nation ABO and Rh blood type distribution by nation (averages for each population) Population O+ A+ B+ AB+ O− A− B− AB− Australia[11] 40% 31% 8% 2% 9% 7% 2% 1% Canada[12] 39% 36% 7.6% 2.5% 7% 6% 1.4% 0.5% Denmark[13] 35% 37% 8% 4% 6% 7% 2% 1% Finland[14] 27% 38% 15% 7% 4% 6% 2% 1% France[15] 36% 37% 9% 3% 6% 7% 1% 1% Hong Kong, China[16] 40% 26% 27% 7% <0.3% <0.3% <0.3% <0.3% Korea, South[17] 27.4% 34.4% 26.8% 11.2% 0.1% 0.1% 0.1% 0.05% Poland[18] 31% 32% 15% 7% 6% 6% 2% 1% Sweden[19] 32% 37% 10% 5% 6% 7% 2% 1% UK[20] 37% 35% 8% 3% 7% 7% 2% 1% USA[21] 38% 34% 9% 3% 7% 6% 2% 1%
  • 11. Blood donors 2006 400 350 300 250 200 150 100 50 0 March January February June April May July August September October November December Month Number of units reg vol auto dir os mc
  • 12. Total Donations 1 2 3 4 5 6
  • 13. Theoretical Yield of components  1 unit of blood theoretically gives 1 unit FFP 1 unit PRBC’s 1 single donor unit cryoprecipitate, single donor unit platelets Plasma for Ig and albumin  In theory 4138 U of FFP, 4138 U PRBC’s, 4138 U cryo 4138 single donor units platelets  In reality 334 U FFP, 2405 U PRBC’s, 46U cryo* 216 U plasma, 409 U platelets*
  • 14. Component use by month 200 180 160 140 120 100 80 60 40 20 0 Number of units FFP use by Month January June November Month Surgery O&G Paeds A&E Medicine
  • 15. 40 35 30 25 20 15 10 5 0 Number of units Plasma use by month January May September Total Month Surgery O&G Paeds A&E Medicine
  • 16. Platelet use by month 40 35 30 25 20 15 10 0 5 March January February June April May July August September October November December Month Number of SD units Surgery O&G Paeds A&E Medicine
  • 17. Discarded Units Whole blood 504 (39%) Packed cells 13 (5%) FFP 29 (9%) Platelets 169 (41%)
  • 18.
  • 20. The Donation Process Education Recruitment Selection Donation
  • 23. Infectious Disease Testing  HIV  Hepatitis B  Hepatitis C  HTLV-I and II  CMV  Malaria  Syphilis*
  • 24. Whole Blood It is now used rarely in current practice in the UK or U.S.A, although in many countries it accounts for most transfusions. Almost all whole blood donations are processed to separate red cells, platelets and plasma.
  • 25. Whole Blood Currently whole blood should only be considered in the following scenario: An adult has bled acutely and massively The adult has already received 5 to 7 units of RBC plus crystalloids
  • 26. Packed red cells 150-200 mls. of red cells with plasma removed  Haemoglobin 20g/ 100 ml, PCV 55-75 Expected rise in Hb with 1 unit of red cells is approximately 1g/dL
  • 27. Indications for Packed Cells Massive blood loss Anaemia of chronic disease Haemoglobinopathies Perioperative period to maintain Hb> 7g/dL No need for transfusion with Hb >10
  • 28. Platelets 150-400 x109 /L Platelet units can be either Single donor units Apheresis units 1 single donor unit contains 55 x109 1 apheresis unit contains 240x109
  • 29. Platelets Stored at room temperature Constantly agitated Only last for 5 days 1 dose of platelets should raise patient’s counts by 30 x109 after 1 hour Infused in 15 mins
  • 30.
  • 31. Indications for platelet transfusion BLEEDING due to thrombocytopaenia Due to platelet dysfunction Prevention of spontaneous bleeding with counts < 20
  • 32. Recommended counts to avoid bleeding Platelet count /ul Clinical Condition > 100 000 Major abdominal, chest or neurosurgery > 50 000 Trauma, major surgery > 30 000 Minor surgical procedures > 20 000 Prevention/treatment of bleeding in pts with sepsis, leukemia, malignancy > 10 000 Uncomplicated malignancy, leukemia > 5 000 ITP patients at low risk
  • 33. FFP Fresh Frozen Plasma Plasma collected from single donor units or by apheresis Frozen within 8 hours of collection -18o to -30o C Can last for a year
  • 34. FFP 1 unit is 250 ml Contains all plasma proteins Indications: Correction of bleeding due to excess warfarin, Vitamin K deficiency, liver disease DIC, dilutional coagulopathy Inherited factor XI deficiency TTP
  • 35. FFP Dose: 15 mls/kg about 3-5 units FFP and INR <2 Give at 1ml/kg per hour in likely fluid overload patients Given within 24 hours of thawing Requesting FFP
  • 36. Frozen Plasma Plasma frozen within 24 hours of collection Maintains level of plasma proteins except factor VIII Same indications as FFP
  • 37. Cryoprecipitate FFP thawed at 4oC and centrifuged Cryoprecipitate is the by-product Contains Fibrinogen, Factor VIII, Factor XIII, von Willebrand’s Factor
  • 38. Cryoprecipitate No longer indicated for Hemophilia* Source of Fibrinogen in acquired coagulopathies as in DIC; platelet dysfunction in uremia Indicated for bleeding in vWD, Factor XIII deficiency
  • 39. Cryoprecipitate Infused as quickly as possible Give within 6 hours of thawing 10-15 mls; usually 10 units pooled 10 bags contain approx. 2gm of fibrinogen and should raise fibrinogen level to 70mg/dL
  • 41. Appropriateness of transfusion May be life-saving May have acute or delayed complications Puts patient at risk unnecessarily ‘ The transfusion of safe blood products to treat any condition leading to significant morbidity or mortality, that cannot be managed by any other means’.
  • 42. Inappropriateness of transfusion Giving blood products for conditions that can otherwise be treated e.g. anaemia Using blood products when other fluids work just as well  Blood is often unnecessarily given to raise a patient’s haemoglobin level before surgery or to allow earlier discharge from hospital. These are rarely valid reasons for transfusion.
  • 43. Inappropriateness of Transfusion Patients’ transfusion requirements can often be minimized by good anaesthetic and surgical management. Blood not needed exposes patient unnecessarily Blood is an expensive, scarce resource. Unnecessary transfusions may cause a shortage of blood products for patients in real need.
  • 44.
  • 45. Problems faced by QEH Too few donors Lack of equipment Insufficient products Insufficient reagent Infectious disease testing
  • 46. Recommendations  Increase public awareness about need for blood and hence the number of voluntary donors  Continue to encourage relatives to donate for patients*  Increase the number of mobile clinics  Extend the opening hours for blood collecting
  • 47. Recommendations  Management of stocks of blood and blood products  Maintenance and replacement of equipment  On-going training of Haematology Lab Staff  Better management of reagents for- infectious disease testing, antigens etc.  Improved record keeping  Move to electronic record keeping
  • 48. Recommendations View to reduce the need for allogeneic transfusions Autologous transfusions Blood saving devices in OR Acute normovolemic haemodilution Oxygen carrying compounds
  • 49.
  • 50. Conclusion ‘Primum-non-nocere’ Weigh risks and benefits Haemoglobin level is not the sole indicator for transfusion Use of appropriate products for the various conditions Personal ethics
  • 51. Credits Blood bank staff Blood collecting staff Dr. T. Laurent Prof. P. Prussia Ms. Kay Bryan
  • 52. Bibliography  Uptodate.com  British Transfusion guidelines 2007  Clinical use of blood, WHO  MJA: Tuckfield et al.,Reduction of inappropriate use of blood products by prospective monitoring of blood forms  Transfusion practice: Palo et al., Population based audit of fresh frozen plasma transfusion practices  Vox Sanguinis: Titlestead et al., Monitoring transfusion practices at two university hospitals  Transfusion: Schramm et al., Influencing blood usage in Germany  Transfusion: Healy et al., Effect of Fresh Frozen Plasma on Prothrombin Time in patients with mild coagulation abnormalities  Transfusion: Sullivan et al., Blood collection and transfusion in the USA in 2001  Transfusion: Triulzi, The art of plasma transfusion therapy

Editor's Notes

  1. Controlled temperature water bath ABO compatibility
  2. Value of mobile clinics, were supposed to have 4 this year only 2 happened. Problems with preparation of rooms, informing personnel at locations by the facilitators
  3. Addition of new antigens in chronically transfused patients.