Welcome to the 5th edition of Life Blood. We trust you have had a productive year thus far and wish you well for the latter period of 2007.


In this edition we focus on paediatric blood products, the return policy of blood products, and WPBTS transport logistics.
In addition, Dr Bridget Farham, editor of the CME journal, has granted us kind permission for the use of articles from the June 2007 (Vol.25 No.6) edition of CME. In this issue we’ve included Haemophilia emergencies, authored by Dr Andrew McDonald and Sr Anne-Louise Cruickshank and Menorrhagia and inherited bleeding disorders, authored by Dr Andrew McDonald.

We value your input so please feel free to contact us with any suggestions for further discussion. You can contact the Medical Department on 021 5076317 or the Marketing Department on 021 5076326, or e-mail marketing@wpbts.org.za

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Paediatric Transfusion Products

The clinical indications for transfusion in neonates and infants may differ from those for adults, as infants are more susceptible to some of the harmful effects of transfusion. For the purpose of these guidelines, neonates are considered to be babies within 4 weeks of their normal gestational age. Infants are babies within the first year of life.

Most neonatal paediatric transfusions are small volume, given to replace the blood losses of investigative sampling or to alleviate the anaemia of prematurity. Larger transfusions are needed for replacement during surgery or pathological blood loss. Replacement in excess of blood volume may occur during cardiac bypass surgery or total blood volume exchange.

Read Further

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Menorrhagia and Inherited Bleeding Disorders

Women bleed – and this is especially so in childbearing years where menstruation
and childbirth represent significant haemostatic challenges. Up to 10 - 15% of women will experience menorrhagia in their lifetime – either as primary (present from menarche) or secondary (developing later in life). While the majority of excess bleeds are not related to haematological disorders, in certain series, bleeding diatheses accounted for 5 - 20% of underlying causes. These may be acquired (low platelets in patients with idiopathic thrombocytopenic purpura (ITP), antiplatelet drugs) or inherited bleeding disorders such as:

  • von Willebrand disease (vWD)
  • inherited platelet dysfunction disorders
  • haemophilia A or B carrier status
  • other rare factor deficiencies.

Read Further

Haemophilia Emergencies

Classic haemophilia is an X-linked disorder, with either a deficiency of factor VIII (haemophilia A), or of factor IX (haemophilia B) being inherited from the mother. Factor VIII and IX, together with phospholipid, form the "tenase" complex which converts factor X to its active form Xa; deficiency of one is clinically indistinguishable from the other, and the diagnosis is made on specific assays and blood levels. This level also serves to categorise the severity, with a factor level of < 1% being severe, 1 - 5% moderate and 5 - 25% mild. The severe and moderately affected individuals are prone to spontaneous bleeding - usually in joints – for which most patients are on home factor replacement therapy. They may, however, also present with spontaneous life threatening bleeds; inappropriate iatrogenic intervention may also be responsible for this situation. For this reason, the emergency poster (Fig. 1) has been prepared and will be widely distributed to emergency units.

Read Further

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WPBTS Blood Return Policy

These guidelines are established to ensure safe transfusion of all blood products.

Red Cell Products
All red cells products can be returned to the Blood Bank for credit, if they conform to all of the following:

  • Returned to the Blood Bank within 24 hours of issue
  • Returned at a temperature between 2 to
    10 oC
  • Returned to the Blood Bank with the cable tie attaching the unit to the container not cut
  • Returned to the Blood Bank with the hermetic seal unbroken

These units will be kept for a further 24 hours for the same patient.

Read Further

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The Transportation of Blood and Blood Products

The WPBTS Transport Department is an essential link in the transportation of blood and blood products. The collection and delivery of blood and blood products is strictly governed by criteria set out in the Standards of Practice with particular focus on the maintenance of the cold chain.

All blood and blood products are handled, stored and transported under optimum conditions to prevent damage and deterioration. Before despatch from our headquarters, the temperature of all blood products is recorded. A temperature record is again taken on arrival at the Blood Banks. These records are kept for purposes of quality assurance and traceability. Appropriate containers and eutectic devices are used, to ensure that optimum temperatures are maintained across all links in the transfusion process – from collection, to processing, to distribution to the blood banks, and subsequently to the hospitals and patients.

Read Further

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Paediatric Transfusion Products
The clinical indications for transfusion in neonates and infants may differ from those for adults.
read more >

Menorrhagia and Inherited Bleeding Disorders
Women bleed – and this is especially so in childbearing years where menstruation
and childbirth represent significant haemostatic challenges.
read more >

Haemophilia Emergencies
Classic haemophilia is an X-linked disorder, with either a deficiency of factor VIII (haemophilia A), or of factor IX (haemophilia B) being inherited from the mother.
read more >

WPBTS Blood Return Policy
Guidelines are established to protect the efficacy of all blood products.
read more >


The Transportation of Blood and Blood Products
The WPBTS Transport Department is an essential link in the transportation of blood and blood products.
read more >



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