patients who decline blood products:- … who decline blood products:-haematological aspects of care...
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Dr Catherine FlynnConsultant Haematologist
CWIUH
Patients who Decline Blood Products:-Haematological Aspects of Care
Bloodless Labour and Delivery in CWIUH!
0100020003000400050006000700080009000
Total deliveries
8500 deliveries in 2009, 2.5% transfused
2.5%
97.5%
Incidence of JW in Ireland
6.5 million Jehovah’s Witnesses in 235 countries worldwide and about 150 000 in Great Britain and Ireland. Estimated 5,000 Jehovah's Witnesses in Ireland
Maternal Morbidity in JW
Mount Sinai study (Singla et al 2001)Netherlands Study (Van Wolfswinkel et al 2009)
2008 Report of Jehovah's Witnesses Worldwide
Peak Witnesses in in 2007 (>140 000)Brazil
Democratic Republic of CongoGermany
ItalyJapanMexicoNigeria
PhilipinesRussiaUkraineZambia
Co existent Hb Disorders
Van Wolfswinkel et al 2009 BJOGNetherlands study 1 JW patient with sickle cell disease
Whole Blood
Red Cells White Cells Platelets Plasma
Oxygen therapeutics**Products in development
Interferons*
Interleukins**Recombinant Products available
Platelet Substitutes**Products in development
Clotting Factor Concentrate* (*VIIa,VIII,IX available)
Prothrombin Complex Concentrate
Fibrinogen
Albumin ±
Immune Globulins
UNACCEPTABLE
PERSONAL DECISION
‘Meeting the clinical challenge of care for Jehovah’s Witnesses’
Bodnaruk et al Trans Med Revs 2004
Platelets in additive solution
Ante-partum
Identify the patient early and discuss optionsInvolve senior peopleIdentify and investigate co-existent risk factors for anaemia/bleedingConsider stopping warfarin/aspirin/clopidrogelMinimise phlebotomy and use paediatric blood tubes for laboratory studiesEstimate bleeding risk (placental position/previous pregnancies)
Define Acceptable Treatment for every PatientPharmacological agents that do not contain
blood productsTransexamic acid/ DDAVP/ Recombinant factor concentratesHaematinics and Growth factorsIron/albumin free erythropoietinSynthetic oxygen carriersNon blood volume expanders
Transfusion Treatment PlanTreatment AcceptPrimary Blood ComponentsRed Cells Yes No
Apheresis Platelets Yes No
Minor FractionsSolvent Detergent Plasma/ Octoplas Yes No
Washed Platelets in Platelet Additive Solution Yes No
Blood ProductsFibrinogen Yes No
Fibrin Glue Yes No
Prothrombin Complex Yes No
Immunoglobulin Yes No
Recombinant Clotting FactorsFactor VIIa Yes No
Factor VIII or IX Yes No
Discuss Alternative Treatment Options
Iron (PO or IV)ErythropoietinTranexamic AcidRecombinant Blood Products
Erythropoietin and Blood Conservation
Albumin free erythropoietin (rHuEPO) enhances erythopoiesisNeoRecormon (Roche) epoetin beta Aranesp(Amgen) darbepoetin alfa
Multiple case reports, few trials
Time to start treatmentDosagesRoute of AdministrationTreatment Duration
Most reported cases use adjunctive iron/folic acid/Vit B12
Variable
Copyright restrictions apply.
Price, S. et al. Anesth Analg 2005;101:325-327
Haematological Variables During admission
Intrapartum/Post Partum
Anaesthetic/Surgical optionsKeep warm, normalise pH as platelets and coagulation factors less functionalConsider positionPrompt oxytoxicsAntifibrinolytics (tranexamic acid/aprotonin)Topical Fibrin Glue (contains a blood fraction)
Antifibrinolytic agentsCyklokapron / Tranexamic acidPotent competitive inhibitor of the activation of plasminogen to plasmin. No evidence in animal studies of a teratogenic effect. Use in pregnant woman is limited/ crosses the placenta A synthetic derivative of the amino acid lysine with antifibrinolytic activity. With strong affinity for the five lysine-binding sites of plasminogen, tranexamic acid competitively inhibits the activation of plasminogen to plasmin, resulting in inhibition of fibrinolysisLonger half-life/ ten times more potent and less toxic than aminocaproic acid
Tranexamic acid/ Cyclokapron
Meta-analysis comparing tranexamic acid with no treatment.
3 major trials involving 461 participants
Transexamic acid versus no treatment and blood loss post delivery
No mortality data
A single dose of 1 gram of tranexamic acid given intravenously
Tranexamic acid may reduce blood loss in post partum haemorrhage
Ferrer et al ,BMC Pregnancy and Childbirth 2009
World Maternal Antifibrinolytic Trial
The WOMAN trial is a large, international, randomised, placebo controlled trial. http://www.thewomantrial.Lshtm.ac.uk.
Tranexamic Acid for the Treatment of Postpartum Haemorrhage: An International Randomised, Double Blind, Placebo Controlled Trial
Options
Identification of the case and optimisation of haematological status of the motherOptimisation of 3rd stage of labourPrompt surgical intervention if necessaryOther agents haematinic support/erythropoiesis stimulants/antifibrinolytics/recombinant blood products
VIIa/Novoseven
Limited to the site of tissue injury and tissue factor exposure. Useful in the obstetric setting where there is often bleeding from a large raw area of exposed tissue. Action of rFVIIa is dependant on the presence of adequate numbers of circulating platelets and adequate fibrinogen concentration.
rFVIIa in major obstetric HaemorrhagerFVIIa should be considered in major obstetric haemorrhage
A dose of 90 μg/kg is recommended
Use of rFVIIa should not be seen as an alternative to surgical haemostasis or correction of coagulopathy with blood products.
Before administration of rFVIIa, the following laboratory indices are desirable; –Prothrombin time < 1.5 × upper limit of normal –Fibrinogen > 1.0 g/L–Platelet count > 50 × 109/L
A pH > 7.1 is also desirable for optimal effect.Bomken et al Obstet Gynecol Int. 2009: 364843.
Post Haemorrhage
Oxygen and erythropoietin 300IU/kg x3 per weekShortens lag period of erythropoiesis and accelerates haemoglobin recoveryIron supplementation essential
Oral iron is slow and unreliableIV iron (Iron Sucrose) (Venofer) 200mg x3/weekAugment with B12 and folic acid
Hyperbaric Oxygen