BloodManagementSession_March08

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    Mary Metcalfe & Carmel Parker.Transfusion Practitioners.

    Ext 8041 bleep 2010 or 8041.

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    To gain understanding of best clinical practiceinvolved in Blood/Blood componets therapy.

    How to safely and appropriately order bloodproducts for transfusion.How to safely set up a transfusion and monitorpatients at this point.

    Management of suspected adverse Transfusionreaction.

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    Patient clinical details and presentation.Up to date blood results.Transfusion history and any adverse events.

    Drug history and dosage.Colleagues, patient, nursing staff, family membersare a viable source of information.Transfusion policy and practitioners, lab staff.

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    EU directive Blood Safety 2002/98/EU.Transposed into law in November 2005.Vein-to-vein traceability.

    Set standards for collection,processing,distribution,testing andstorage of products.

    Record keeping extended to 30 YEARS.!!

    Operational Impact Group

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    Check the patients details and case note history.Are special requirements needed? E.g. CMV orirradiated.

    Use the indication codes for RBC & FFP.Is it an appropriate transfusion, what are thealternatives?Is it an EMERGENCY or is it routine.

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    Aims of thesession

    Station 1.HospitalBlood

    Bank/products.

    Station 2.Venous

    Sampling - risk

    Station 3. Bloodadministration

    TransfusionReactions/Review

    & feedback

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    NEAR MISS EVENTS 1997/98 - 2003 (n=2427)

    57%

    14%

    11%

    10%

    8%

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    Acute blood loss R1To maintain circulating blood volume and Hb>7g/dl Peri-operative, assuming normovolaemia R2 Hb < 7 g/dlR3 Hb < 9 g/dl in presence of cardiovascular disease or

    significant risk factors for cardiovascular diseaseR4 Critical care: Transfuse to maintain Hb > 7 g/dl(>9g/dl if at risk as R3)

    R5 Post-chemotherapy; there is no evidence base guideto practice usually Hb 8 or 9 g/dl

    R6 Radiotherapy: transfuse to maintain Hb > 10 g/dlR7 Chronic Anaemia: transfuse to maintain thehaemoglobin just above lowest concentration that is

    not associated with symptoms of anaemia.

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    Check the patients case note

    Transfusion historySpecial requirements- e.g., irradiated, CMV negative

    Complete request form or ordercommunications

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    CasenoteSurname

    Forename

    DOBEthnic Origin

    LocationConsultantSex

    Patient Category NHSDate of Request

    Entered byOriginatorDate of Specimen

    Service (Type of Request)Blood Group

    Previous Transfusion

    Units (amount) Date ReqdReaction

    Specimen typeVacutainer 7mls pink + 4.5 mls EDTA

    Antibodies

    Specimen taken by Sign and print Name Requesting Medic Sign and Print name

    Copy of this request must be filed in the notes. See Trust Transfusion policy

    Diagnosis, referral reason, relevant medication

    Information found on the RequestForms

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    Step 1: Ask the patient to tell you their:

    Full Name + Date of Birth

    Be extra vigilant when checking the identity of theunconscious / compromised patient

    Check this information againstthe patients ID wristband

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    Only bleed one patient at a time usingAseptic non touch techniqueDo NOT use pre-labeled tubesLabel the sample tube beside the patient

    Send the sample to the laboratory in themost appropriate way for the clinicalsituation, i.e. routine / emergency

    Remember emergency requests mustalways be phoned through to theTransfusion Laboratory.

    Sampling Procedure

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    Labelling the venous blood sample

    Information to include:-Full nameDate of birthHospital numberGenderDateSignature of person who has taken the

    sampleAt the bedsideBy the person taking the sample

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    Positive Patient Identification

    I cdnuolt blveiee that I cluod aulacltyuesdnatnrd what I was rdgnieg

    The phaonmneal pweor of the hmuan mnid

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    Patient X bled into a pre-labelled sample tube withpatient Ys details Patient Y (23 year old) experienced a post-ophaemorrhage

    Patient Y was Group O and received a unit of groupA red cellsPatient complained of loin pain - transfusion reactionqueried but transfusion continued

    Patient developed renal failurePatient died as a direct result of incompatibletransfusion

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    IV Blood/ Blood Component Chart

    Observations must be recorded please ensure all detail are

    complete on the prescription chart e.g. all patient details .

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    Blood TransfusionAdministration

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    Found on all Wards/Units & Hospital Intranet

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    Decision to Transfuse Communicate with patientPatient information leaflet

    Document in patient notes

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    Minimum Transfusion Dataset: the following should bedocumented in the notes

    Reason for transfusionCurrent blood resultsComponent type and amount to be prescribedAnticipated outcomeAny reported transfusion adverseevents/reactions

    Review following the transfusion including howmuch blood has been transfused

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    There are no special requirements and selection

    would be dependant on the desired infusion rate

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    WHY WARM BLOOD ?

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    1 PATIENTS UNDERGOING SURGERY WILLALREADY BE LOSING BODY HEAT DUE TOWOUND OR CAVITY EXPOSURE

    2 LARGE VOLUMES OF COLD BLOOD MAYINDUCE HYPOTHERMIA OR CARDIACARYTHMIAS

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    3 Exchange transfusion

    4 If requested by the laboratory. i.e.. The patienthas cold agglutinins

    Never warm blood by any other method

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    1st checkersRegistered Nurse/ Midwife or

    Sick Childrens Nurse, Doctor& a qualified Agency Nursethat holds a Trust contract

    2nd Checkers

    Any of the above &

    Qualified Theatre Practitioner

    or qualified agency nurse thatdoes not hold a TrustContract.

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    Base line observations Temperature, pulse and bloodpressure

    Further observations (as above) at 15 minutes

    A set of observations at the end of transfusion

    More frequently if the patient is unwell, unobservable,unconscious or a child.

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    Ensure the venflon is secure, patent and there areno signs of inflammationGive the patient the call bell

    Patients should remain in a clinical area for theduration of the TransfusionReview the patients fluid balance and medication.

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    LEAKSDISCOLOURATIO

    NCLUMPINGEXPIRY DATE

    If there is ANY discrepancy - DO NOT transfuse

    Pre-administration Procedure

    Step 3: Undertake visual inspection

    Step 1: Check the blood component has been prescribedStep 2: Undertake baseline observations

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    Pre-administration checks

    Personal checks:- ANTT- wear personal protective equipment

    Equipment checks:- Personal protective equipment is available andis clean and sterile- A correctly completed prescription chart

    - Observation chart- Giving set- Disposable bags- Trolley

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    Be extra vigilant when checking the identity of theunconscious / compromised patient

    Step 1: Ask the patient to tell you their:Full Name + Date of Birth

    Check this informationagainst the patients IDwristband

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    Step 2: Check the patients First name Surname Date of birth Hospital number

    on the compatibility/

    traceability label againstthe patients ID wristband

    Administration Procedure

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    Any discrepancies DO

    NOT TRANSFUSE !

    Administration ProcedureStep 3: Check the compatibility/traceability label with theblood bag label

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    Stop the Transfusion and seek Medical Input and inform theTransfusion Laboratory staff

    Check the Blood component matches the patient details

    Replace the unit and giving set with Normal Saline 0.9%Send the discontinued unit with giving set attached back totransfusion capped off at the end with a white venflon cap and any previous transfused bags sealed with the blue plugsall in biohazard bags

    Documentation (complete the checklist)

    Complete a Trust Incident form

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    Signs:Fever

    (1.5 C rise)TachycardiaHypotension

    HaemoglobinaemiaHaemoglobinuria

    Generalised oozingfrom wounds

    Symptoms: Apprehension AgitationFlushingPain at cannula sitePain in abdomen, flankOr chest

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    Fever and any other symptoms/signs ofhaemolysis more than 24 hours after transfusionUnexpected fall in HbMay have postive Direct Antiglobulin test(Coombs test) or positive crossmatchConsider sending samples to the NBS

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    Non-Haemolytic Febrile (Fever) TransfusionReaction

    Between 1-2% of transfused patients experiencesome sort of febrile reaction

    Caused by antibodies in the patients plasma reacting

    against the leucocytes in the donors blood

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    Fever or rigor 30 - 60 minutes after thestart of the unit +/- rash

    TREATMENT:

    Stop the transfusion

    Give antipyretic e.g. Paracetamol +/- PiritonContinue transfusion if symptomes subside.

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    Transfusions of blood & blood componentsare labour intensive & expensive but arefrequently life saving events

    In a few patients, however they can result inpotentially fatal complications

    It is therefore essential that they are onlygiven when the benefits outweigh the risks

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    The donors blood (the graft) mounts animmune response against the recipient (the

    Host)

    There is no effective treatment and thecondition is nearly always fatal

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    Platelet antibodies from the donor destroythe recipients platelets

    These lowered platelet levels cause bleedingfrom micro vessels in to the skin.

    This manifests as purple areas ( purpura ) seenon the patients skin

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    DefinitionThrombocytopenia within 12 days after transfusion

    of red cells, associated with the presence in thepatient of antibodies directed again the HPAsystems.Need to exclude DICNeed to send blood for HPA typing and antibody

    screen

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    Viral infections screened for at the time ofdonation

    Bacterial infections from contaminated bloodcomponents

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    Each unit of blood contains 250 mg of iron

    For patients on long term transfusion therapythis starts to accumulate and become toxic

    causing damage to the liver heart, pancreasand organs of the endocrine system

    Drug therapy is given to excrete this excess

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    Fluid OverloadCaused when too much fluid is transfused orthe transfusion is to rapid

    Signs & Symptoms includeAcute Left ventricular failure,dyspnoea,Hypotension, Tachycardia raised jugularvenous pressure

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    Signs & Symptoms can range from:

    Mild and common (estimated risk 1 in100Urticaria (a raised red itching rash) Treated with anantihisamine with the transfusion beingrecommenced if the symptoms subside

    ToRare (estimated risk 1 in 500,000)but very severe and sometimes fatal anaphylaxismanifesting in:- low BP, laboured breathing oroedema, respiratory and cardiac arrest respiratory &cardiac arrest

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    Caused by antibodies in the donors plasmareacting strongly with the patients leucocytes

    Signs & Symptoms

    Transfusion is followed by a rapid onset ofbreathlessness and non productive coughChest x ray characteristically shows bilateralpulmonary infiltrates or white out

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    Acute dyspnoea with hypoxia and bilateralpulmonary infiltrates during or within 6 hours oftransfusionInform transfusion as soon as possibleTreat as adult respiratory distress syndromeNeed to inform the National Blood Service

    Wh t i thi ? Wh t i ith it?

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    What is this? What is wrong with it?What would you do if you saw it?

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    Can occur during collection, storage & thehandling processes

    Bacterial ContaminationEstimated frequency

    per unit

    Red Cells 1/500,000

    Platelets 1/12,000

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    An Acute medical emergency Caused by ABO incompatible transfused red cells.

    Probably due to misidentification of

    The patientThe product

    orThe sample

    Seek Haematology Input immediately

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    Stop the Transfusion and seek Medical Input and inform theTransfusion Laboratory staff

    Check the Blood component matches the patient details

    Replace the unit and giving set with Normal Saline 0.9%

    Send the discontinued unit with giving set attached back totransfusion capped off at the end with a white venflon cap and any previous transfused bags sealed with the blue plugs allin biohazard bags

    Documentation (complete the checklist)

    Complete a Trust Incident form

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    Transfusions of blood & blood componentsare labour intensive & expensive but arefrequently life saving

    In a few patients, however they can result inpotentially fatal complications.

    It is therefore essential that they are onlygiven when the benefits outweigh the risks