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    EXCHANGE BLOOD

    TRANSFUSION

    BY

    DR H.C. ANYABOLU

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    EXCHANGE BLOOD TRANSFUSION

    Dr. Anyabolu

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    Brief History

    Definitions Indication

    Equipment

    The Procedure Monitoring

    Post Exchange Care

    Complications Controversies

    Recent Trends

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    BRIEF HISTORYHart (1925)Superior Sagittal

    Sinus (out) andSapherious Vein (in).

    Werner & Wexlar (1946)Radial

    Artery( out )andSaphenous

    Vein (in)

    Diamond (1946)Umbilical Vein

    (out and in)Sanchez (1960) Umbilical Venous cut

    down

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    INDICATIONS1. In severe hyperbilirubinema

    * In hemolytic disease at birth if

    PCV 5mg/dl or reticulocyte> 15%

    * Rate of bilirubin rise >

    0.5mg/dl/hr or >5mg/dl/day.* Kernicterus, irrespective of

    serum bilirubin level

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    * In preterm LBW babies, rule

    of 10

    * Lower values of bilirubin in

    the presence of complication

    eg. hypoalbuminema,

    asphyxia, acidosis, hypoxia,hypothermia, sepsis, IVH,

    hypoglycaemia.

    * Serum bilirubin close toexchange value for > 36hrs.

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    2. Severe anaemia (PCV

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    8. Vasocclusive Cases in SCD* Priapism in Maiduguri (Ahmed

    SG et al 2002)

    After 6unitscompletedetumescence

    - 95% Hbs 30.3% Hbs

    * Prevents the 1st stroke and

    also recurrence e.g. The 9yrgirl from Ilesha (Senbanjo et al

    2005)

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    9. Hyperparasitemia in Malaria* Especially with early end

    organ failure

    * Whole blood or reconstituted

    red cells* Single, 1.5% or double

    volume

    * 70% 2% in parasites

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    10.Babeiosis, Trypanosomiasis11.Pertussis(Romans MJ et al

    2004)12.Kwashiorkor with severeanaemia in CCF.

    13.Immunological Diseases- TSI in neonatal

    thyrotoxicosis

    - SLE (Olowu 2006)

    - Myasthenia gravis

    - Gullain Barre Syndrome

    (Baranwal et al 2006)

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    14.Inborn Error of MetabolismNeonatal hyperammonemia

    15.Acute Hepatic Failure

    16.LeukaemiaLeucostasis withhyperviscosity

    17.PoisoningsSalicylate,sedatives, theophylline, snake

    envenomation.

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    EQUIPMENT1. Mask/sterile gown/gloves2. Umbilical catheter/cannula (2)/

    IV set/ arterial line with

    Transducerchoice depend onwhich method.

    3. Dressing pack

    4. Sterile green drape

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    5. Haematology/Biochemistry

    bottles and request form

    6. Blood waste bag

    7. Heparin flush solution

    8. Blood giving set9. Cardiorespiratory monitor

    10.Resuscitation apparatus

    11.Pacifier

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    PROCEDUREConsent

    Blood/Blood Product

    Type Depends on thecondition

    Choices include wholeblood, packed red cells,reconstituted PRBC + FFP

    Group Depends on thecondition (Rh dix, ABOdix)

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    Haemocrit at least 40%

    Genotype important in SCDx

    G6PD status important in G6PD

    defc.

    AgeMost studies < 48hrs old (fresh)- Fresh, unbanked in DIC

    Microbial ScreeningHIV, Hepatitis,

    malariaSyphilis, CMV -

    irradiation

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    AnticoagulantsHeparin most

    preferred (no

    acidosis, electrolytederangement,

    hypocalcemia.

    Drawbacks

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    SettingFree from Human Traffic- Well lighted

    - Ambient temperature

    250C - 300C (may need

    incubator or radiant

    heater)

    AsepsisStrict- Patient on sterile drapes

    - Personnel on sterile

    gowns, gloves and masks

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    Personnel1 Doctor and 1 nursewith another competent doctor

    within shouting distance

    GI Preparation NPO for 34 hrs- Stomach should

    be aspirated

    before and during,

    in very sick babies

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    Patient RestraintCrucifix

    - Formica boardPriming25% albumin 1g/kg 1 -

    2hrs before the

    procedure(controversial)- Heparin solution flush

    2000units + 250mls of

    saline

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    Vascular AccessNeonates,umbilical vein

    Older children, femoral vein

    Others: * great saphenous vein

    * umbilical artery

    * radial artery

    * superficial temporal

    arterySite in Umbilical Vein- not >7cm

    Peripheralaccess

    (indications)

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    Volume ExchangedSingle volume- Double volume

    - Partial Exchange

    N/B * Blood volume: Neonates 80

    100ml/kg others 6070mls/kg

    Aliquots20mls in well termbabies less in sick babies

    - 5mls/kg in preterm

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    DurationMinimum 45mins but notmore than 90mins.Ideally, every 100mls

    exchange = 15mins

    Drugs - 10% calcium gluconate 1mlper 100ml of blood

    (*controversial)

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    MONITOR AND CHART Temperature, Heart Rate;

    Respiration, Blood Pressure Portal venous pressure (not >

    10mmH2O)

    pH, PaO2

    RBS (Dextrostix)

    Colour cyanosis

    Blood warmer at 35370C

    Input and Output

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    LAST BLOOD WITHDRAWN

    PCV, B1B2, RBS, Ca2+, Na+, K+,

    Mg2+,

    B1B2 6hrs & 24hrs (rebound)

    Blood Culture if indicated

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    POST EXCHANGE CARE1. Monitor vital signs 1/2hrly x 2

    hrly x 2 4hrly x 6 6hrly x 2

    2. Observe catheter sites for

    bleeding

    3. Abd. Girth measurements

    4. Observe stools for blood

    5. N.P.O. for at least 3hours.

    However must be on dextrose

    containing fluid.

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    6. Remove umbilical catheters with a

    stitch in the vein. Cover with saline

    soaked gauze. Send catheter tip form/c/s

    7. Babies on antibiotics or

    anticonvulsants should be re-

    medicated8. Jaundiced babies should continue

    phototherapy.

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    9. Repeat portal venous pressure

    10.Prophylactic antibiotics

    individual merit

    11.CARRY PARENTS ALONG.

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    COMPLICATION

    Metabolic .Acidosis

    .Alkalosis (later)

    . k+, Na , Glu, Ca2+,

    Mg2+

    . Hypo/Hyperthemia

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    CARDIORESPIRATORY

    - Volume overload

    - Arrhythmia- Apnea

    - Cardiac arrest

    - Hypotension- Bradycardia

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    GIT - Bowel perforation

    - Inspissated bile syndrome

    - NECVASCULARPortal vein thrombosis

    and hypertension

    - Umbilical vessel

    perforation- Portal abscess

    - Vasospasm

    - IVH.

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    COMPLICATION OF BLOOD PRODUCTS-Infection

    -Thrombocytopenia-Air embolism

    -Thromboembolism

    -Anaemia (early & late)-GVH reaction

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    Prevalence of complications

    3% of neonates have transfusion

    reaction usually mildSignificant morbidity5% ( in

    recent times).

    Deaths3 in 1000 procedures(highly dependent on premorbidstate).

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    CONTROVERSIES

    - Use of calcium gluconate

    - Benefit in kernicterus

    RECENT DEVELOPMENTS

    Automationfaster, wastes

    less blood, lesscirculatory

    fluctuation, more

    aseptic. Procedures are less frequent.

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