Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Programme: - Introduction - How to define.

Slides:



Advertisements
Similar presentations
Endothelial Progenitor Cell (EPC) Core Laboratory Instructions Version 5.0 March 29, 2008 For questions regarding collection, processing, storage, or shipping.
Advertisements

Separation of blood components
Part 2 Terry Kotrla, MS, MT(ASCP)BB
Blood Bag Coagulation & Preservers Citrate 24 hours 1-6 ºC Heparin 48 hours 1-6 ºC ACD or CPD 21 days 1-6 ºC CPD-A135 days 1-6 ºC CPD-A1+ additive.
Leukopak Processing.
IMMUNOLOGY LABORATORY PBMC ISOLATION SOP by Kizza D Martin Ssemambo
Yr 12 Biology: Research Assessment Part B – Blood By Peter Rowlands.
Blood Components Dosage And Their Administration
1 5/8/2015 Seven Day Storage At 4°C Of Previously -80°C Frozen AB Plasma Sm. Remco Strelitski, BSc Chief Lab technician, Military Blood Bank, Netherlands.
Components Preparation By: Wajnat Tounsi. Why preserve blood?! To provide patients who need blood components transfusion with VIABILE products. RBCs viability.
Intra operative blood conservation
Introduction of « TRIMA » in a Regional Blood Transfusion Organisation Dr Bernard LAMY.
Buffy Coat Method Platelet Poor Plasma Step 1: Whole Blood is collected into a top and bottom pack and is centrifuged (hard spin) to produce platelet poor.
BLOOD BANKING 1- BLOOD PRODUCTS 2- AUTOLOGOUS TRANSFUSION M. H. Shaheen Maadi Armed Forces Hospital.
Blood Components.
DDr.Susheela Innah Professor &HoD Dept of Transfusion Medicine Jubilee Mission Medical College, Thrissur.
Microhematocrit.
THE URINARY SYSTEM.
Glucose test Ms. Ibtisam alaswad Ms. Nour A. taim.
Jessie Maher. What is the composition of blood? Plasma -55% of the blood is plasma - Liquid section that transports blood cells around your body, with.
BLOOD TRANSFUSION Begashaw M (MD).
Unit 2 Blood and Blood Components
TRANSFUSION MEDICINE MBBS,MCPS,FCPS. Professor of Pathology
GURU BRAHMA GURU VISHNU GURU DEVO MAHESWARAHA GURU SHATHSHATH
+ Dr. Megan Rowley Consultant in Transfusion Medicine Blood Transfusion.
Federico Voglino – PM SE & ME Region Compomat ® G4.
TSE Advisory Committee October 14, 2004, Silver Spring, MD Removal of blood-borne TSE infectivity by leukoreduction filters Luisa Gregori V.A. Medical.
BLOOD COMPONENT PREPARATION
BY : Dr. Beenish Zaki, Instructor Department of Biochemistry (15 February 2012)
Apheresis Blood Components
Pictorial Guide To The RCV Procedure
Leukocyte-Reduced Blood Components Lore Fields MT(ASCP)SBB Consumer Safety Officer, DBA, OBRR, CBER September 16, 2009.
Removal of Infectious Prions from Red Cell Concentrates Samuel Coker, PhD Principal Scientist and Technical Director Pall Medical Transmissible Spongiform.
Module 1: The Journey of Blood: Donation to Distribution Transfusion Training Workshop KKM 2012.
QUALITY ASSURANCE & QUALITY CONTROL OF BLOOD COMPONENTS
Blood By: Sophie Gollan. Consists of two main parts: Plasma – Blood plasma is a mixture of proteins, enzymes, nutrients, wastes, hormones and gases. -
FDA Update: Particulate Matter Task Force Sharyn Orton, Ph.D. OBRR/CBER/FDA Blood Products Advisory Committee Meeting June 19, 2003.
The Massive Transfusion Protocol An Aide Memoire 1.
Preparation of blood components
Microhematocrit Determination. Microhematocrit Hematocrit — Test that provides a health care worker with an estimate of the patient’s red cell volume.
Chapter 16 Circulation. Section 2 Blood – Blood is made up of four components: plasma, red blood cells, white blood cells, and platelets – Plasma – Red.
Infusion Kit compatibility James Baker - CHAOTIC 2 nd November
Blood Transfusion Safe Practice.
Autotransfusion (“Cell Savers”): rev
What is DNA purification? Lyse cells or tissues Inactive endogenous nucleases Separate DNA from other cellular components – Proteins – Lipids – RNA – Others.
Volunteer Training Double Red Cell Donation COL-COPY (AA) This training material is a template which Blood centers can use to help draft their training.
Sample Collection Bayer recommendations BNP is unstable in glass containers Recommended sample type is EDTA plasma using plastic tubes for sample collection.
DNA extraction. Total DNA: whole blood (fresh or frozen), plasma, serum, buffy coat, body fluids, lymphocytes and cultured cells. This technology first.
Chapter 21 Blood.
WITH MCS+ AND TRIMA SEPARATORS.
BLOOD & BLOOD PRODUCTS.
Determination of Hematocrit value (H)
The common lysis solutions contain A. sodium chloride.
Blood Preservation and Storage
Benefits of apheresis collection
Platelet-Rich Plasma Augmentation for Hip Arthroscopy
Pictorial Guide To The RCV Procedure
Coombs test practical(3)
Topics Discussed Today
The development of LPPC in PAS in Blood Transfusion Centre, Faculty of Medicine, Khon Kaen University, Thailand Jongkol Akahat, Thipaporn Jaroonsirimaneekul,
REDOXS Training: Introduction & Site Investigator
Topics Discussed Today
Blood.
Intraoperative Cell Salvage
Process Control in a Component Laboratory
Introduction To Medical Technology
Blood Components Dosage And Their Administration
Practical Blood Bank Lab 11 Cyroglobulin.
COLLECT PATIENT BLOOD SAMPLE • Draw one (1) SST tube (Serum Separator Tube) from each patient using standard venipuncture technique • Allow blood to clot.
Presentation transcript:

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Programme: - Introduction - How to define logistics of bloodprocessing - Priority of components - Influence of regulations - Influence of staff related regulations - Influence of platelets production - Example of optimised logistics - TSF separation and bloodbank logistics

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Define priority of bloodcomponents Optimalisation of blood components: Production of ALL components in MOST excellent quality is NOT possible, define priority: - Plasma; quick separation, fast freezing to optimise quality. Freezing < 3 hr after separation - Platelets, storage for 4 – 24 hours, optimal recovery of platelets, high quality. -This choice of most important component together with method of preparation defines basic algoritms of processing, find acceptable consensus for all components.

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Influencing the logistics of blood processing External regulations: - Fractionater; max. delay of freezing 3 hr - GMP; different staf for different departments Internal influences: - Organisational priorities; lab and processing - waste costs; - work during late evening/night; personal costs

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Parameters effecting logistics: method of preparation and choice of bag system. Different Reduction in Lymphocyte and Granulocyte content by removal of BC from fresh and O/N stored blood. (Z.Rácz, Hungary 1997) - Results of separation: Manual (Q), Separator 1 =TACE(Q) and Separator 2=OPTIPRESS) were compaired with these variabels: - Fresh blood and stored (O/N) - Different sizes of BC taken - Distribution of Lymphocytes/Granulocytes were investigated.

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Top and Bottom separation: -Simultanious transfer of Plasma and Red Cells. - Buffycoat is NOT transferred - Hard spin for maximal Plasma recovery, up to 4700g for 15 minutes.

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Conventional Quadruple bag: - Removal of plasma and BC from top of primairy bag. - Transfer of SAGM through same tube. - Quality of components influenced by storage of blood - Platelet production with pooled Single BC or single Dilted BC

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Results of the study: - Stored blood gives better removal of leukocytes with equal volume of BC removed ml BC: FreshStored - Manual Q: 45%70% - Auto Q:60%78% - Auto TAB:71%82%

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Platelet production Platelet production from whole blood: Triple bag conventional: Platelet Rich Plasma, to be separated by an additional spin in PC and PPP. Quadruple bag conventional: A: Diluted buffy coat to be separated by additional spin in PC and a waste residual BC. B: 4 – 6 single buffycoats to be pooled together with a plasma (or additive solution), to produce a pooled random platelet concentrate. Buffycoats to be pooled within 24 HOURS

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Basic Processing procedures Platelet production from whole blood: Quadruple TAB bag : Diluted buffycoat to be separated by additional spin in PC and a waste BC. Better results as quadruple Dil BC Triple TAB bag: Single buffy coat to be pooled together with 4-6 and a plasma (PAS etc), to produce a pooled random platelet concentrate. Buffycoats to be pooled within 24 HOURS

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Basic Processing procedures PERFORMANCE OF SEPARATION TABCONV QTriple PRP Plasma recovery L-reduction RCC+++++/+- Platelet recovery Separation time2 – 7 min2 – 3 min2 Spin Syphonage effectyesnono Disposable cost++++++

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL QUALITY OF DIFFERENT COMPONENTS

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Optimal separation logistics in Rotterdam (NL). - Collection of blood: every day from 09:00 untill 21:00. The collected blood is stored O/N in a incubator of 22°C. - Test samples of blood are tested during the night from 00:00 untill 07:00. -Test results are used to release the collected blood before the processing starts at 08:00. - Unsafe blood is processed separate of safe blood. - Pooling of Buffycoats is always done with safe products, no waste of pools due to positive test results.

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Alternative for platelet production: Terumo Saving Platelet filter 3 leukodepleted products RBC, PLASMA, PLTS in 1 LGF version: results in small “BC” Some recent tests done:

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Results of TSF: Elverum; Norway (5000 col year ) Pool of 4, with T-SOL (BC 24hr old) Buffycoat: weight is gr netto. Redcell loss: ml in BC. Diluted BC 10 ml plasma. Pool: Volume of ML, HcT= 21 – 23 % (recovery of pooling: 97%) Results: Pooled 6 pools, Plt recovery: 294 – 356 x 10 9 unit Recovery of second separation: 75 – 93% of pool

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Results of TSF: Maribor, Slovenia: 9 – 13 May Pool of 5 BC with PLASMA Buffycoat: weight is gr netto. Redcell loss: ml in BC. Diluted BC 10 ml plasma. Pooled buffycoats of different ages: -Overnight stored -Two days stored (aggitated) -Three and four days stored (aggitated)

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL Results of TSF: Maribor, Slovenia: 9 – 13 May Fresh pooled: (O/N): 240 – 380 Day 2: 342 and 348 Day 3: 332 and 93 (cherry coloured BC’s!!) Day 4: still under investigation. Recovery of pooling: 99% Recovery of sec separation: 75% (1950 rpm 4 m 30 sec) % (1300 rpm for 7 min, acc 8, brake 1)

Transfusion Systems Transfusion Business CompanyTRANSFUSION CONGRESS Opatia, Croatia June 10-11, 2005 CONFIDENTIAL New posibility for TSF saving Platelets Small centres, willing to pool BC, allowing them to have prestorage filtering conditions with pooling untill day 3 (or more) to optimise the logistics of the platelets.

Platelet pooling with BP-KIT + IGIIII-S PL Filter holder += BPKIT with IGIII S-PL –Buffy-coat pooling kit with soft housing platelet filter High yield leukodepleted platelet conc.