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Error Management in Blood Collection
Dr. Ravneet Kaur Professor & Head Department of Transfusion Medicine GMCH, Chandigarh
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Regulated and technically specific blood collection process is vital
Provide safe blood Preparation of high quality blood component
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Multi-tier process Donor Education/ Pre donation counseling
Detail history of prospective donor Physical examination Phlebotomy Post donation care and counseling Error …… Harmful to donor as well as recipient
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Errors…….
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Error – Donor counseling/ Physical examination
Ne photograph Error – Donor counseling/ Physical examination
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Error – Preparation of blood bag ( wrong expiry date)
New photograph Error – Preparation of blood bag ( wrong expiry date)
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Registration no. 110670 Blood bag marked O positive Blood bag group A positive
Blood bag marked A positive Blood bag group O positive Error – Improper identification of pilot tubes
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Blood bag & pilot tube prepared
Donor registration no Blood bag & pilot tube prepared Donor deferred - Poor vein Next day – First donor – same registration no. Pilot tubes missing from Donor complex Pilot tubes with blood sample traced in laboratory area Error – Wrong identification of Pilot Tubes
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Error – Over collection / Under collection
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Error – Inadequate mixing / Inadequate flow
Clot Error – Inadequate mixing / Inadequate flow
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Error – Improper sealing of tubal segment after blood collection
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Errors in blood collection
Technical errors Improper preparation of venipuncture site Faulty technique Inadequate mixing of blood with anticoagulant/ volume collected Sampling error Sample collected in wrong pilot tube Non collection of blood sample Improper sealing Inappropriate discarding of needle Clerical errors Improper donor identification Improper preparation of blood bag Wrong identification number on the blood bag Wrong collection/expiry date on the blood bag Mislabeling of pilot tubes
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Error Management Error prevention Error analysis
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Error Prevention Appropriate Standard Operating Procedure
Training of staff & continuous motivation/education Validated and functioning equipment
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Standard Operating Procedure - Donor blood collection
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Pre donation information /Counseling
Conducted By trained staff with counseling skill In a separate room Should include Information regarding eligibility criteria, blood donation process, TTI and various test performed Pre donation risk assessment for TTI Informed written consent
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Physical examination Donor should be in good health
Detailed history…….High risk behavior Meet the standard criteria for donor selection Donor weight, blood pressure, hemoglobin
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Donor identification Critical to the safety of both donor and recipient Numeric or alphanumeric system to identify the donor Segment no. of the blood bag Photograph of segment no and registration sticker to be added
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Preparation of blood bag
Correct identification number Blood bag Satellite bag Donor record (registration card) Pilot tubes Appropriate date of collection and expiry New photograph to be added
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Phlebotomy Carry out hand cleaning before and after each procedure
Should wear well fitting gloves
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Preparation of venipuncture site
Inspection of both anticubital fossae Skin preparation by aseptic technique 70% isopropyl alcohol & tincture of iodine Concentric spiral manner (centre to periphery) Area – 3 inches ; contact time – 30 seconds NO TOUCH - Venipuncture technique Prepared site must not be touched again. Do not repalpate the vein at the intended venipuncture site
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Single clean venipuncture Performed by trained phlebotomist
Phlebotomy Single clean venipuncture Adequate flow Performed by trained phlebotomist
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Phlebotomy Ensure proper mixing with anticoagulant
Collect adequate volume
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Desired volume X Sp.gravity + Weight of empty bag with anticoagulant
Weight of blood bag Desired volume X Sp.gravity Weight of empty bag with anticoagulant = 350 x = 448gms ± 10%
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350 ml Blood Bag 450 ml Blood bag Normal ml / gm ml / gm Low volume PRBC ml / gm ml / gm Under collection < 233 ml / 325 gm < 300 ml / 409 gm Over collection > 385ml / 485 gm > 495 ml / 614 gm Blood bag should be appropriately labeled – Low volume, Under collection, over collection
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Never leave the donor alone Sample collection at bedside
New photograph to be added Never leave the donor alone Re check the registration no. Sample collection at bedside
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Appropriate discarding of needle
Phlebotomy Proper sealing Appropriate discarding of needle
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Proper storage Adequate temperature Up right position
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Post donation care Guide donor to refreshment room
Give post donation instructions Provide contact information of the transfusion centre
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Training Must to ensure that all staff members are undertaking critical processes are competent to perform task Should include Induction training for new staff Refresher training Intimation of any change Training program Principles, procedures – SOP Principles of good manufacturing practice Safety requirement for staff Training programme should be conducted for new staff and refresher training especially for the tasks that may not be performed on a regular process. When ever any change is made in any of the procedure it should be intimated to all . The training programme should be based on Standard operating procedure and should through light on principles of good manufacturing practice so that staff understands the potential consequences of not following SOP. Stress should also be laid the safety requirement to be followed by the staff members.
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Equipment Periodic maintenance and calibration should be carried and documented according to established procedures
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Blood collection in blood donation camps
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Camp site Organized in a way
Ensures safety of blood donors, staff & donated units Avoids errors in blood collection
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Camp site Waiting area Screening / Physical examination area
Phlebotomy area Refreshment area Close watch on the donors
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Transport of blood Maintain temperature not more than 10°C during storage and transport Secure the lid tight shut Not to exceed the capacity of boxes
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Automation in blood collection
Unique set of bar coded identification number for identifying blood bags, samples and records Helps to avoid manual/clerical errors
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Medical event reporting system for Transfusion Medicine
Capture threats, hazards, near misses, injuries, and deaths systematically Can identify error where action is required Raises staff awareness about error management Blood centers can benefit from identifying and tracking their events and errors and near misses. It helps to identify system attributes and factors that may per dispose to error. One such reporting system that can be used is MERS- TM ;Can identify error where action is required
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Root Cause Analysis of Error
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Documentation Record information Pertaining to donor
Adverse donor reaction Any deviation from Standard Operating Procedure Errors reported and corrective action taken
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Conclusion Strictly adhere to Standard Operating Procedures
Errors should be analyzed and documented Helps to identify areas where resources need to be targeted Improves over all safety of transfusion
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Thank you
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