Sitemap
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Overview
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3.1 Clinical Governance
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3.2 Prescribing Blood Components and Fractionated Products
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3.3 Informed Consent to Receive a Blood Transfusion
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3.4 Requesting Blood Components and Fractionated Products
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3.5 Blood Stock Management: the Maximum Blood Order Schedule
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3.6 Collecting Blood Samples for Pre-transfusion Testing
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3.7 Pretransfusion Testing
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3.8 Patients With a Positive Antibody Screen
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3.9 Sample Validity (‘72-hour Rule’)
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3.10 Provision of Red Cells in an Emergency
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3.11 Removal From Storage and Time Limits for Transfusion
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3.12 Administration and Observation of Transfusion
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3.13 Rate of Transfusion and Precautions
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3.14 Electromechanical Infusion Pumps
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3.15 Blood Administration Sets and Filters
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3.16 Warming of Blood Components
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3.17 Compatible Intravenous Solutions
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3.18 Adding Medication to Blood Components
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3.19 Documentation of Transfusion
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3.20 Local Systems and Procedures
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3.21 Reporting of Adverse Events