12.07.2015 Views

IBTS DIAG GDE 0001 - Irish Blood Transfusion Service

IBTS DIAG GDE 0001 - Irish Blood Transfusion Service

IBTS DIAG GDE 0001 - Irish Blood Transfusion Service

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<strong>IBTS</strong>/<strong>DIAG</strong>/<strong>GDE</strong>/<strong>0001</strong> Ver. 2 Page 13 of 415.6 Quality of <strong>Blood</strong> Specimens (Vis–à-Vis Condition and Timing)Specimens for Compatibility testing should be referred to the laboratory without delay tofacilitate timely testing of the specimens and processing of requests5.6.1 Timing of Specimen Collection in relation to Previous <strong>Transfusion</strong>.<strong>Transfusion</strong>s or pregnancy may stimulate the production of unexpected antibodies througheither a primary or secondary response. The timing of specimens selected for crossmatching orantibody screening must take account of this. (See guidelines Section 12.1 and 12.2)5.6.2 Crossmatching Requests, Reference Specimens.In situations where patients are being repeatedly transfused (e.g. AIHA, SCD, etc) a dailyspecimen is not a requirement. These patients should be screened with a fresh specimen for thedevelopment of irregular antibodies at least every 72 hours, with the agreement of <strong>IBTS</strong> and thepatient’s clinician.In the case of pregnant women who are booked for elective caesarean section and who may notpresent to the hospital until shortly before surgery, specimens used for pre-transfusion testingin these patients should never be more than 7 days old and where possible, it is advisable that aspecimen taken immediately before transfusion be made available for retrospective testing inthe event of a transfusion reaction occurring.Note:The user must be aware that the presence of haemolysis or clots may make the specimens unsuitable forprocessing.Where specimens are found to be unsuitable on receipt at the <strong>IBTS</strong> Diagnostics Laboratory, a secondspecimen will be requested.5.7 Non-Conforming Specimen Bottles, Forms or Specimen Quality IssuesWhere the requirements with respect to labelling of the request form/ specimen container orspecimen quality issues are not met, the following will apply.

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