# Standard Operating Procedure: Blood Transfusion Administration | Document ID | SOP-BB-002 | |-------------|-------------| | Title | Blood Transfusion Administration | | Revision | 1.0 | | Effective Date | [DATE] | | Author | [AUTHOR] | | Approved By | [APPROVER] | | Department | Transfusion Services | --- ## 1. Purpose To establish standardized procedures for the safe administration of blood and blood components to minimize transfusion errors and adverse reactions. ## 2. Scope This procedure applies to the administration of: - Packed red blood cells (PRBCs) - Fresh frozen plasma (FFP) - Platelets (random donor and apheresis) - Cryoprecipitate - Granulocytes ## 3. Responsibilities ### 3.1 Ordering Physician - Determine transfusion indication - Order appropriate blood component - Obtain informed consent - Respond to transfusion reactions ### 3.2 Blood Bank/Transfusion Service - Perform compatibility testing - Issue blood products - Maintain inventory - Investigate transfusion reactions ### 3.3 Nursing Staff - Verify patient identity and blood product - Administer transfusion - Monitor for reactions - Document transfusion ## 4. Definitions | Term | Definition | |------|------------| | Crossmatch | Compatibility test between donor RBCs and recipient serum | | Type and Screen | ABO/Rh typing and antibody screen | | Transfusion Reaction | Adverse response to blood transfusion | | Emergency Release | Issue of uncrossmatched blood in emergencies | ## 5. Procedure ### 5.1 Pre-Transfusion 1. **Physician Order Review** - Verify order includes: - Patient identification - Blood product type - Number of units - Rate/duration - Special requirements (irradiated, CMV-negative, etc.) - Confirm indication appropriate 2. **Type and Screen/Crossmatch** - Collect sample per specimen requirements - Label at bedside with two identifiers - Complete blood bank request form - Allow time for testing (45 min - 1 hour typical) 3. **Informed Consent** - Explain benefits and risks - Discuss alternatives - Answer patient questions - Obtain written consent (FRM-BB-003) - Document in medical record 4. **Pre-Transfusion Assessment** - Baseline vital signs: - Temperature - Pulse - Respiratory rate - Blood pressure - Assess IV access (18-20 gauge preferred) - Review history of previous reactions ### 5.2 Blood Product Issue 1. **Request Blood from Blood Bank** - Verify order and patient identification - Note any special requirements - Confirm expected time of transfusion 2. **Blood Bank Verification (Issue)** - Match unit to patient (ABO, Rh, crossmatch) - Check expiration date - Inspect unit for abnormalities: - Hemolysis - Clots - Discoloration - Bag integrity 3. **Transport** - Transport promptly (within 30 minutes) - Do not store in nursing unit refrigerators - Return to blood bank if transfusion delayed >30 min ### 5.3 Bedside Verification (CRITICAL) **Two qualified staff must verify at bedside:** | Item to Verify | Check | |----------------|-------| | Patient wristband name matches blood bag | ☐ | | Patient wristband MRN matches blood bag | ☐ | | Patient wristband DOB matches blood bag | ☐ | | ABO/Rh on blood bag matches compatibility label | ☐ | | Unit number on blood bag matches compatibility label | ☐ | | Expiration date is valid | ☐ | | Blood product type matches order | ☐ | | Blood bag appears normal (no clots, hemolysis) | ☐ | | Patient confirms identity (if possible) | ☐ | **DO NOT TRANSFUSE IF ANY DISCREPANCY EXISTS** ### 5.4 Transfusion Administration 1. **Blood Administration Set** - Use blood administration set with 170-260 micron filter - Prime set with normal saline only - Never add medications to blood products - Maximum hang time: 4 hours 2. **Compatible IV Fluids** | Compatible | NOT Compatible | |------------|----------------| | 0.9% Normal Saline | Lactated Ringer's | | | Dextrose solutions | | | Medications | 3. **Infusion Rates** | Product | Initial Rate (first 15 min) | Routine Rate | Maximum Time | |---------|---------------------------|--------------|--------------| | PRBCs | 2 mL/min (50 mL) | Per order/tolerance | 4 hours | | FFP | 2 mL/min | 10 mL/min or per order | 4 hours | | Platelets | 2 mL/min | Per tolerance | 4 hours | | Cryoprecipitate | 2 mL/min | Per tolerance | 4 hours | 4. **Monitoring Schedule** | Time | Action | |------|--------| | Pre-transfusion | Baseline vital signs | | 15 minutes | Vital signs + assessment | | 30 minutes | Vital signs | | Hourly | Vital signs | | Post-transfusion | Final vital signs + assessment | ### 5.5 Transfusion Reaction Management **Signs/Symptoms Requiring Immediate Action:** - Fever (≥1°C rise) - Chills/rigors - Hypotension or hypertension - Tachycardia - Dyspnea/respiratory distress - Chest or back pain - Hives/urticaria/rash - Nausea/vomiting - Hemoglobinuria (dark urine) - Anxiety/sense of doom **Immediate Response:** 1. STOP the transfusion immediately 2. Keep IV line open with normal saline 3. Notify physician immediately 4. Check vital signs 5. Verify patient/blood product identities 6. Notify blood bank 7. Complete FRM-BB-004 Transfusion Reaction Report 8. Return blood bag and tubing to blood bank 9. Collect post-reaction blood and urine samples **Reaction Workup** | Sample | Purpose | |--------|---------| | EDTA tube (lavender) | DAT, visual hemolysis check | | Clot tube (red/gold) | Repeat crossmatch, visual hemolysis | | First voided urine | Hemoglobinuria | | Blood cultures | If bacterial contamination suspected | ### 5.6 Post-Transfusion 1. **Documentation** - Product type and unit number - Start and end times - Volume transfused - Vital signs (all) - Adverse reactions (or "none") - Patient response 2. **Disposition of Blood Bag** - Per facility policy (typically to blood bank) - Retain for minimum time specified ## 6. Special Situations ### 6.1 Emergency/Massive Transfusion - O-negative PRBCs for females of childbearing potential - O-positive PRBCs for others acceptable in emergencies - Type-specific blood as soon as available - Activate massive transfusion protocol if indicated ### 6.2 Pediatric Transfusion - Adjusted volumes (10-15 mL/kg) - Smaller filter volumes - Consider irradiated products ## 7. Documentation - FRM-BB-003 Transfusion Consent Form - FRM-BB-004 Transfusion Reaction Report - Transfusion Record (in EMR or paper) - Blood bank compatibility record ## 8. References - AABB Standards for Blood Banks and Transfusion Services - AABB Technical Manual - FDA regulations 21 CFR 606 - Circular of Information for Blood and Blood Components --- ## Revision History | Rev | Date | Description | Author | |-----|------|-------------|--------| | 1.0 | [DATE] | Initial release | [AUTHOR] |