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Patient Software Requirements Specifications

Patient - Investigation of Adverse Effects

Allows entry of transfusion reaction data that is unrelated to a specific unit. (Requires a higher level of access).

Patient - Investigation of Adverse Effects

Provides report of transfusion data, sorted by patient, including both reactions associated with a specific unit and those not associated with specific units.

Patient - Investigation of Adverse Effects

Provides report for use in identifying potential cases of transfusion transmitted disease, based on search of those patients transfused within the previous 6 month period for specific patient test results using facility specified tests and facility defined values.

Patient - Management/Quality Improvement

Provides a report of crossmatch transfusion ratios, sorted by treating specialty, in either summary or detailed format to allow a review of ordering patterns.

Patient - Management/Quality Improvement

Provides a report of patients crossmatched for a specified date range, sorted by date/time crossmatched, to allow a review of ordering patterns. The report includes specimen info, unit ID, XM result, outcome of XM (released or transfused) and statistics on the # of patients crossmatched, # of specimens crossmatched, # of units transfused, the C T ratio and the # of crossmatches for each result (C, IG, etc.).

Patient - Management/Quality Improvement

Provides a report of autologous unit dispositions, sorted by whether the unit was transfused or not, including the patient information, treating specialty if unit was transfused, component, unit ID and the number of days in inventory, to allow evaluation of utilization patterns.

Patient - Management/Quality Improvement

Provides a mechanism to identify units with a prolonged infusion time, based on component specific local parameters for maximum infusion time, i.e. entries in the BLOOD PRODUCT file (#66).

Patient - Management/Quality Improvement

Provides an administrative data report which details data requested on the annual AABB questionnaire, sorted into inventory and donor groupings.

Patient - Management/Quality Improvement

Provides a report of potentially inappropriate transfusions based on the auditing done during specimen log-in /order entry, sorted by location to which the unit was issued for transfusion.

Patient - Management/Quality Improvement

Provides a patient report, which can be used for outcome assessments, integrating transfusion episodes and clinical lab results for site selected tests. User can request the report for specific patients and date ranges or specify that reports should be printed for all patients transfused within a specified date range.

SRS# P86

P87

P88

P89

P90

P91

P92

P93

P94

P95

P96

Functionality Patient - Investigation of Adverse Effects

Description

Updates cumulative patient transfusion record, including data on clinically significant antibodies, transfusion reactions and units transfused, immediately upon data entry.

Appendix H-38

Laboratory V. 5.2 Blood Bank User Manual

August 1998

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