Platelets
Platelet transfusions are indicated for the prevention and treatment of haemorrhage in patients with thrombocytopenia or platelet function defects. Platelets for transfusion can be prepared by centrifuging a whole blood donation or collected by the process of plateletpheresis (platelet component donation). In this book the component is termed ‘platelet concentrate’. Platelets prepared by each method have similar efficacy, but use of apheresis platelets exposes the recipient to the blood of fewer donors. Currently platelet concentrates contain a substantial volume of plasma, required to maintain platelet function during storage, although the use of platelet additive solutions allows the amount of plasma to be reduced. Platelet function is best maintained by storage at 22°C with agitation. As this temperature favours growth of some bacteria, culture of platelet concentrates prior to release from storage is being introduced to reduce the small risk of a unit being contaminated with bacteria.
The usual dose unit for an adult is referred to as an ‘adult dose unit’. It should contain 2.5−3 x 1011 platelets. In practice the dose is often defined in terms of the number of whole blood donations (typically four to six) that are pooled to provide the dose. Alternatively a single plateletpheresis procedure can provide an adult dose unit from a single donor.
Pathogen-reduced platelets
Platelet concentrates can be treated to reduce or inactivate microbial infectivity (not vCJD). Clinical trials have indicated that the product is efficacious. This process has not yet been introduced in the UK. A similar process has been developed for red cells, but the product has encountered problems during clinical trials.
Table 3 Platelets
From whole blood donations: platelets from 4 or 5 donations constitute an adult therapeutic dose (ATD) From apheresis: 1 donor collection provides 1 to 3 ATDs |
From whole blood | mean | sd | 95% CI | range |
Number of donors | 4 | | | |
Volume ml | 310 | ± 33 | 317−321 | 250−400 |
Platelets x 109 (at least 240 x 109) | 330 | ± 50 | 329−332 | 180−400 |
Plasma ml | 250 | | | |
Anticoagulant ml | 60 | | | |
White cells per unit | 0.3 x 106 per pack | | | |
From apheresis | mean | sd | 95% CI | range |
Number of donors | 1 | | | |
Volume ml | 215 | ± 53 | 206−207 | 180−300 |
Platelets x 109 | 290 | ± 45 | 289−291 | 180−400 |
Plasma ml | 180 | | | |
Anticoagulant ml | 35 | | | |
White cells per unit | 0.3 x 106per pack | | | |
Storage | 5 days at 22 ± 2°C on a special agitator rack (may be extended to 7 days if system is validated and in conjunction with bacterial testing) |
Compatibility requirement | Preferably ABO and RhD identical with patient |
Dosing guide | For a 70 kg adult, 1 ATD typically gives an immediate rise in platelet count of 20−40 x 109 ml |
Administration | Infuse through a standard blood administration set or a platelet infusion set − use a fresh set when administering each infusion of platelets |
Cautions | RhD negative females with potential for childbearing must be given RhD negative platelets to avoid risk of Rh sensitisation (see RhD antigen and antibody) Plasma in the platelets can cause an ABO incompatibility reaction (see ABO blood groups and antibodies), TRALI (see TRALI) or allergic reaction (see Allergic reactions) |
Source: NBS and SNBTS routine QA data |
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