thromboembolism 7- 5-15
TRANSCRIPT
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A 19 days old baby, was delivered by LUCS at 35 weeks of gestation weighing 2100 g, was completely well upto 15 days. He developed jaundice & treated with phototherapy. After two days he got normal saline bolus, antibiotics and blood transfusion for septic shock. 2 hours following blood transfusion his lower extremities became cyanosed with progressive blackening of both feet and legs. Peripheral pulses were absent in both lower limbs. Baby was diagnosed as Preterm (35 weeks) LBW (2100 g), LONS, neonatal jaundice, thromboembolism. Immediate consultation from vascular surgeon taken, Heparin infusion started and antibiotics changed. Since then baby’s condition is gradually improving.
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Thromboembolism in newborn Dr. Md Hanif Sumon Resident (Phase-A) Dept. of Neonatology BSMMU
Dr. Md. Shameem Resident (Phase-B) Dept. of Neonatology BSMMU
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Normal haemostatic mechanism
There are four phases to the normal coagulation cascade:Blood vessel
constrictionPlatelet aggregationFibrin generationVessel repair and
fibrin degradation
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Basic steps of blood coagulation
3 Basic steps of blood coagulation:
Step-1 :Generation of prothrombin activator(Factor-x) by extrensic or intrinsic pathway.
Step-2: Conversion of prothrombin to thrombin by prothrombin activator.
Step-3: Conversion of fibrinogen to fibrin(clot) by thrombin.
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Intrinsic clotting system
The intrinsic clotting pathway requires at least four coagulation proteins and two co-factors.
Tested using the aPTT.
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Activation of intrinsic pathway
The intrinsic pathway is initiated by the exposure of blood to a negatively charged surface and activation of Factor XII.
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Extrinsic clotting system
The extrinsic system, in contrast, requires only one coagulation protein and two co-factors (Ca & TF ).
Extrinsic pathway is assed
with PT.
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Activation of extrinsic pathway
Tissue thromboplastin (tissue factor) is present on the surface of perivascular tissue cells but is only exposed to blood flow during injury.
Thromboplastin, in the presence of calcium, binds to Factor VII to cause the activation of Factor X.
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The two pathways feed into the common pathway
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Physiology
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Fibrinolysis To restore vessel
patency, the clot must be organized and removed by plasmin while wound healing and tissue remodeling occur.
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Abnormal hemostatic mechanisms
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Pathophysiology Thrombus is a solid mass formed in the circulation from the
constitution of the blood during life. It is composed of : Fibrin Platelets Red cells Fate of thrombus: Propagation : complete obstruction
Embolization Dissolution by fibrinolytic activity Organization and recanalization
Embolus Any intravascular solid, liquid or gaseous mass carried by the blood to a site distant from its point of origin. 99% arise from thrombi, so the term thromboembolism.
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Virchow Triad in Thrombosis
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Hemostatic system of neonate
Hemorrhage > thrombosisThe vascular endothelium system has not accumulated
damage from disease or acquired factor.Levels of vitamin K related clotting factor are low.Antithrombin, protein C, protein S levels are low.Decreased fibrinolytic potential.
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Epidemiology Thrombosis occurs more frequently in the neonatal period than
at any other age in childhood. 2.4 per 1,000 admissions to the NICU in Canada 5.1 per 100,000 live births in Germany Male and female equal<10% is idiopathic.
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RISK FACTORS Indwelling vascular catheter is the single greatest risk factor for
arterial or venous thrombosis. Indwelling catheters are responsible for >80% of venous and
90% of arterial thrombotic complications. Others:Maternal: autoimmune disorder, PROM, IUGR, diabetes, pre-
eclampsia, oligohydramnios, prothrombotic disorder, chrioamnionitis, family history of thrombosis, antiphospholipid or anticardiolipin antibody.
Delivery: instrumentation, traumatic delivery, emergency cesarean section. FHR abnormalities
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Neonate: prematurity, sepsis, birth asphyxia, dehydration, congenital heart disease, polycythemia, SGA, RDS, NEC, pulmonary HTN, congenital nephrotic syndrome, DIC, prothrombotic disorder, shock.
Inherited: protein C & S deficiency, antithrombin deficiency, factor 5 leiden mutation, prothrombin G20210A mutation & others.
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Types of Neonatal Thrombotic Disorders
1) Inherited thrombotic Disorders 2) Acquired thrombotic disorders
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Inherited thrombotic Disorders
Protein C deficiency Protein S deficiency Anti-thrombin deficiency Factor v Leiden Prothrombin20210A mutation
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Acquired thrombotic disorders Catheter-related thrombosis Venous thrombosis Arterial thrombosis
Non-Catheter-related thrombosis Renal vein thrombosis
Neonatal stroke
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Inherited thrombotic Disorders
Early age of onset, Spontaneous thrombotic events Extensive venous thrombosis Ischemic skin lesions or purpura fulminans A positive family H/O neonatal purpura fulminans
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SPECIFIC CLINICAL CONDITIONS …. Venous thrombosis : Deep vein thrombosisDifficult to determineMay be clinically silentPresent with swelling and discoloration of limb or face
and head, superior vena cava syndromeMay progress to pulmonary embolism or neonatal stroke
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Right atrial thrombosis:Thrombosis of superior vena cava with
extension in to the right atrium6% of all neonatal thrombosis>50% asympmtomatic, detected incidentally
during echo50% present with respiratory distress, new
murmur, heart failure, tachyarrythmia
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Renal vein thrombosis:Upto 10% of venous thrombosis in newborn80% of non catheter related thrombosis.Common on the left sideClassical triad includes hematuria, palpable
abdominal mass and thrombocytopenia.Other features- HTN, proteinuria, renal impairment.USG- enlarge echogenic kidneys with attenuation or
loss of cortico-medullary differentiation.Color flow doppler- absence of flow in the main or
arcuate renal veinComplication : adrenal hemorrhage, renal failure,
HTN
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Venous thrombosis: cerebral sinovenous thrombosis
Thrombosis of cerebral veins or dural sinusSuperior and lateral sinuses most frequently
involvedPresent with seizure, apnea, lethargy
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Arterial thrombosis: arterial ischemic stroke (AIS)Mostly occur in middle cerebral artery of left
hemisphere.AIS is a common underlying cause of neonatal
seizures in full term newborn.Present with seizures, apnea, asymmetrical
motor development, hemiplagia.Long term morbidity in 1/3rd affected newborn
are hemiparesis, speech delay, language delay.
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Arterial thrombosis: Purpura fulminansRare, rapidly progressive, often fatal Present with DIC and hemorrhagic necrosis of
the skin due to dermal vessel thrombosis.Due to protein C or S deficiency
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Approach to thromboembolismHistory:
Family history of such disorderMaternal history of SLE and/or anti-phospholipid
synPositive risk factorTreatment history
Physical Examination:Assessment of severity
Area of involvement Skin color & compare with other extremity- whether
swollen, cyanotic, hyperemic, discolored, distended superficial vein
Pulses of affected extremityPresence of any catheterAssessment of vital organ function.
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Laboratory studies1. Coagulation profile: PT, aPTT, TT, plasma fibrinogen
conc.2. Hct3. Platelet count: thrombus itself and heparin can cause
thrombocytopenia4. Genetic test: Protein C and S activity levels
Antithrombin activity assay,Factor V G1691A (Leiden mutation), Prothrombin G 20210A.
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Imaging and other studyAccording to organ involvement:Real-time USG with color doppler for diagnosis
and monitoring.Contrast angiography ( the gold standard)Contrast venographyA plain radiograph of the abdomen for catheter
placement.USG or CT of head for sinovenous thrombosis or
IVH.MRA for ischemic neonatal stroke
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“Recommendations for neonatal treatment are based on -
extrapolation of principles of therapy from older children & adult guidelines,
limited clinical information from registries, individual case studies and knowledge of current common clinical
practice”
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Management of Neonatal Thrombosis
Supportive careAnticoagulation ThrombolysisSurgeryCounseling
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Supportive care:Prompt removal of catheter if possibleEmergency consultationLocal care of the woundElevation of footTreamtent of
volume depletion Electrolyte imbalanceSepsisAnemiaThrombocytopenia
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Choice of therapy Small asymptomatic non-occlusive arterial or venous
thrombi related to catheters: Catheter removal and supportive care . Large or occlusive arterial /venous thrombi : Anticoagulation with heparin or LMWH Massive venous thrombi or arterial thrombi: Thrombolysis
Surgery [NB- Oral anticoagulant drugs – not recommnaded for neonate]
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AnticoagulationUnfractionated heparin:
Heparin binds with antithrombin III (AT), causing conformational change that inactivates thrombin and other proteases most notably factor Xa.
Target aPTT level 60-85 secondsDuration 5-14 days but can be used upto 3 months.Reversal agent protaminComplications : Bleeding, Heparin-induced thrombocytopenia,
osteoporosis
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Unfractionated Heparin Dosage MonitoringDose Check APTT
loading 75 U/Kg After 4 hrsMaintenance 28 U/Kg/hr Daily or 4 hrs after dose
changeAdjust APTT level as below:
APTT <50 sec Increase by 20% After 4 hrsAPTT 50-59 sec 10% 4 hrs
APTT 60-85 sec ---------------------- 24 hrsAPTT 86-120 sec Decrease by 10% 4 hrsAPTT >120 Stop for 1 hr then
decrease by 15% 4 hrs
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LMWH (Enoxaparin)Has less effect on thrombin compared to heparin,
but about the same effect on Factor Xa.Duration 5 days to 6 monthsside effects : No major bleeds in premature
neonates Soreness from injection/catheter, leakage, bruising .
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LMWH
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Dosage Monitoring and Adjustment of LMWH
LMW Heparin(ENOXAPARIN)Dose 1.5 mg/kg/dose twice dailyMonitoring anti-factor Xa Level (Therapeutic level
is 0.5—1.0 U/ml)
Check 4-6 hrs after first dose( if in therapeutic range check once weekly)
If dose adjusted recheck after 4 hrs.If <0.35 units/ml , Increase by 25%If 0.35-0.49 U/ml , increase by 10%If 1.1 -2 U/ml, decrease by 20-30%If >2 U/ml withhold until <0.5 & restart at 40% of original dose.
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Comparison of UFH and LMWHHeparin LMWH
1. Requires IV access2. Short term
anticoagulation(3 days to 3 weeks)3. More side effects 4. needs continuous
monitroing
1. Subcutaneous injection2. Long term anticoagulation( upto 6 months)3. Fewer side effects4. Needs less monitoring
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Goal- to degrade fibrindissolve fibrin clot
Indication: Not recommended unless major vessel occlusion causing critical organ or limb compromise.
Outcome: In older children vascular patency 50% with anticoagulant therapy, following thrombolytic therapy > 90%.
If thrombolytic treatment >24 hours monitor plasminogen conc or FFP infusion.
Treatment with heparin after thrombolytic therapy is recommended.
Thrombolytic Therapy
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Thrombolytic Agents
tPA : No loading dose 0.1-0.6 mg/kg/h over 6 h
followed by heparin
Streptokinase: Loading-2,000 U/kg over 10 min then 1,000-2,000 U/kg/h .Only one course should be given
for 6 h
Urokinase:
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Contraindications to Thrombolytic/Anticoagulation Therapy
AbsoluteCNS surgery or ischemia (including birth
asphyxia) within 10 daysActive bleedingInvasive procedures within 72 hoursSeizures within 48 hours
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RelativePlatelet count < 50000/cmm (100000/cmm for
ill neonates)Fibrinogen concentration < 100mg/dLSevere coagulation deficiencyHypertension
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Surgical thrombectomyNot done in majority of neonates Microsurgery with thrombolytic regimen is
successfully used in few isolated cases.
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PrecautionsIntramuscular (IM) injections and arterial punctures
during anticoagulation or thrombolytic therapy should be avoided.
Indomethacin or other antiplatelet drugs during therapy should be avoided. .
Use minimal physical manipulation of the patient. Thrombolytic therapy should not be initiated in the presence
of active bleeding.
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Monitor for thromboembolic complication in all newborn with any catheter.
heparin is often added to neonatal infusions as it prolongs patency
Umbilical lines should be removed as early as possible. UAC <5 days and UVC < 14 days
Prefer a peripheral arterial lines If there is difficulty infusing consider thrombotic eventUse UAC with a hole at the end not at the sideA PICC lines has lower incidence of thrombosis.
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