Employee Information Agency staff, please use your assigned 4 digit ID. Core staff must use UTMB employee ID Emp ID First Last Workplace Using the appropriate selection box below, please select your area of workplace. Note: TDC, Agency, and Medical Students may be selected using the Hospital Service selection box. Hospital Service -----SELECT SITE----- Austin Women's Hospital **** Old John Sealy **** OR - PACU OR HOLDING ***JS Towers (select one)*** J2A/B/C L&D J2D - BICU J3A/B - Ante-Partum J3C - Newborn Nsy J3D - ISCU J4A - SICU J4B - MICU/CCU J4C/D - Cardiac Cath Lab J5A/B -GCRC J6C/D Ante/Post Partum J7D - Med/Surg J8A - Day Surgery J8B - Dialysis J8C/D - Ante/Post Partum J9D - Transplant J10A - Pedi J10C/D - ACE Unit ---TDCJ (Select One) --- TDC 6A - Day Surg TDC 6B - Surgery TDC 6C - Women's TDC 7A - Telemetry TDC 7B - Med ***MISC*** ER/ FAST TRACK ENDOSCOPY OTHER I have read the Guaiac Policy and Procedure Yes Click on START TEST to begin Test Date: START TEST 1. Electronic quality control (EQC) should be performed (note: instrument will lock out if EQC has not been performed). once per month at change of operators once per shift when instrument is in use once per week 2. The Hemochron Response has the following data management capabilities: Tracking of Operator ID, Electronic QC, Tube Lot No, Patient ID, and test results. FALSE TRUE 3. The acceptable patient sample size for FTC 510 tubes is _____; _____ for P214 Pedi tubes. 4 mL; 0.5 mL 1 mL; 0.3 mL 2 mL; 0.4 mL 4. Wet (Liquid) Quality Control should be performed: when a new box of tubes is opened when test tubes are exposed to temperatures outside the recommended range shift in clinical results is experienced after monitor has been dropped All of the above 5. When running a patient sample, FTC-510 tubes must be shaken end to end 10 times (P214-pedi tubes must be flicked 5-7 times) upon sample application: TRUE FALSE 6. Temperature verification for the Hemochron ACT instrument is required every _________ while the filter must be CLEANED (bottom of instrument) every __________. 6 months; month 12 months; 6 months
Hospital Service -----SELECT SITE----- Austin Women's Hospital **** Old John Sealy **** OR - PACU OR HOLDING ***JS Towers (select one)*** J2A/B/C L&D J2D - BICU J3A/B - Ante-Partum J3C - Newborn Nsy J3D - ISCU J4A - SICU J4B - MICU/CCU J4C/D - Cardiac Cath Lab J5A/B -GCRC J6C/D Ante/Post Partum J7D - Med/Surg J8A - Day Surgery J8B - Dialysis J8C/D - Ante/Post Partum J9D - Transplant J10A - Pedi J10C/D - ACE Unit ---TDCJ (Select One) --- TDC 6A - Day Surg TDC 6B - Surgery TDC 6C - Women's TDC 7A - Telemetry TDC 7B - Med ***MISC*** ER/ FAST TRACK ENDOSCOPY OTHER
I have read the Guaiac Policy and Procedure Yes
Click on START TEST to begin
START TEST
1. Electronic quality control (EQC) should be performed (note: instrument will lock out if EQC has not been performed).
once per month at change of operators once per shift when instrument is in use once per week
2. The Hemochron Response has the following data management capabilities: Tracking of Operator ID, Electronic QC, Tube Lot No, Patient ID, and test results.
FALSE TRUE
3. The acceptable patient sample size for FTC 510 tubes is _____; _____ for P214 Pedi tubes.
4 mL; 0.5 mL 1 mL; 0.3 mL 2 mL; 0.4 mL
4. Wet (Liquid) Quality Control should be performed:
when a new box of tubes is opened when test tubes are exposed to temperatures outside the recommended range shift in clinical results is experienced after monitor has been dropped All of the above
5. When running a patient sample, FTC-510 tubes must be shaken end to end 10 times (P214-pedi tubes must be flicked 5-7 times) upon sample application:
TRUE FALSE
6. Temperature verification for the Hemochron ACT instrument is required every _________ while the filter must be CLEANED (bottom of instrument) every __________.
6 months; month 12 months; 6 months
