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DVT IN PREGNANCY.ppt

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Thromboembolism in pregnancy
Thromboembolism in pregnancy
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DVT IN PREGNANCY.ppt

  1. 1. DR LAICHENA
  2. 2. Outline  Definition  Pathophysiology  History  Predisposing factors  Examination findings  Differentials  Investigations  Treatment  Complications  Prognosis  Prophylaxis  Conclusion
  3. 3. DEFINITION It is the formation of a blood clot or clots within the venous vascular cavity. Incidence Exact incidence isn’t known because most studies are limited by the inherent inaccuracy of clinical diagnoses. 1 in 1000 pregnancies. Pregnancy is a hypercoagulable state A pregnant woman has a fivefold risk of DVT compared to general population. Caesarean section increases the incidence by 1-2% Mortality Death from DVT is attributable to massive pulmonary embolism.
  4. 4. Epidemiology  Pregnancy and puerperium are well-established risk factors for venous thromboembolism (VTE)  The age-adjusted incidence ranges from 5 to 50 times higher in pregnant versus non-pregnant women
  5. 5. Epidemiology  Complicates 1 in 500-2000 pregnancies  More common post partum  Antepartum risk is equally distributed across trimesters  Twice as higher after a caesarean section than vaginal delivery
  6. 6. Hemostasis  Formation of clots in the walls of damaged blood vessels  Prevention of blood loss  Maintaining blood in a fluid state within the vascular system
  7. 7. Hemostasis  Components of hemostasis  Vascular spasm  Initiation and formation of platelet plug  Propagation of coagulation cascade  Termination of antithrombotic control mechanisms  Removal of clot by fibrinolysis
  8. 8. Clotting cascade
  9. 9. Hemostasis  Control mechanisms and termination of clotting  Antithrombin, heparin and glucosaminoglycan heparan sulfate  Activated protein C and S  Tissue factor pathway inhibitor  Prostacyclin and thromboxane  Nitric oxide
  10. 10. Clot elimination and fibrinolysis
  11. 11. Anatomical changes in pregnancy and peuperium  Venous Stasis  Gravid uterus  Low capacitance vessels  Immobilisation  Endothelial injury  vascular injury and changes at the uteroplacental surface during delivery  instrumental, or surgical delivery
  12. 12. Coagulation changes in pregnancy  Increase in levels of Fibrinogen by 50% (450mg/dl cf. 300mg/dl)  Other factors increased: Factor VII, VIII, IX, X  Factor II (prothrombin) increased slightly  Factors XI, XII & protein S reduced  Resistance to activated protein C.  Decreased platelet per unit volume
  13. 13. Pathophysiology Vascular clotting develops mainly due to circulating stasis, infection, vascular damage, or increased coagulabiltiy of blood All elements of Virchow’s triad; circulatory stasis, vascular damage and hypercoagulability of blood are present during pregnancy and puerperium. Virchow’s triad is more in pregnancy due to:- i. Increased clotting factors VII, VIII and X ii. Increase in caliber of capacitance vessels produces vascular stasis. iii. Reduced fibrinolytic activity iv. Pressure of the gravid uterus on pelvic veins reduces venous return v. Antenatal rest, prolonged labour, dehydration, excessive blood loss, pressure on the calf muscles during delivery, delay in mobilization, trauma and pelvic infection. vi. Vascular injury after delivery Sites  Posterior tibial and popliteal veins of the calf muscle and extend proximally as far as the femoral or iliac veins or rarely even in into the IVC(Inferior Vena Cava).  Pelvic veins due to diminished blood flow in the hyper-trophied uterine veins extending into the iliac veins
  14. 14. HISTORY The symptoms and signs of Deep Venous thrombosis(DVT) are related to the degree of obstruction to venous outflow and inflammation of the vessel wall. Clinical diagnoses of DVT is neither specific or sensitive with the false positive rate as high as 50%. Many patients are asymptomatic however the history may include the classical features which are;- o Edema/Leg swelling of affected site of the legs o Leg pain (50% of patients) and pain on dorsiflexion of the leg(Homan’s sign) o Tenderness(75% of patients) o Local cyanosis o Fever o Warmth and erythema of the skin can be present over area of thrombosis
  15. 15. Risk factors  Immobilization  Surgery  Obesity  Prior history of VTE  Trauma  Thrombophilias  Prior use of oral contraceptives  Pregnancy or postpartum status  Stroke  Malignancy
  16. 16. PREDISPOSING FACTORS  Thrombophilia Inherited thrombophilias are conditions that increase the risk of thromboembolic disease. During pregnancy, the thrombogenic potential of these disorders is enhanced because of pregnancy- associated changes in several coagulation factors.  There are two types of thrombophlias: Acquired thrombompilias. Inherited thrombompilias
  17. 17. Acquired Thrombophilias  Also called antiphospholipid syndrome.  Presence in the serum of at least one type of autoantibody known as an antiphospholipid antibody (aPL). Lupus anticoagulant antibodies Anticardiolipin antibody antibodies  Their presence predispose to risk of thromboembolism and other obstetric morbidities( recurrent abortions, preeclampsia, stillbirths)
  18. 18. Inherited Thrombophilias  Are genetic conditions that increase the risk of thromboembolic disease. And other obstetric morbidities( abortions, Preeclamsia, IUGR,stillbirths) Factor V Leiden, the most common cause of activated protein C resistance Prothrombin gene mutation (PGM) Antithrombin (AT) deficiency Protein C deficiency Protein S deficiency
  19. 19. Clinical presentation  DVT is more common in the left than the right leg.  WHY
  20. 20. Reason  Increased venous stasis in the left leg due to compression of the left iliac vein by the right iliac artery,  Compression of the inferior vena cava by the gravid uterus itself
  21. 21. EXAMINATION FINDINGS/SIGNS 1) Edema of affected limb usually unilateral.Commoner on the left as the left common iliac vein is crossed by the right common iliac & left internal iliac arteries thus increasing resistance to flow. A circumference of 2-3cm greater in the affected limb than in the normal limb 10 cm from the tibial tuberosity and 20cm from ASIS(Anterior Superior Iliac Spine) 2) Pain and tenderness usually confined to the calf muscles or acting along the course of the deep veins in the medial thigh. 3) Fever usually low grade. 4) Homan’s sign i.e. discomfort in the calf muscles on forced dorsiflexion of the foot with the knee straight. (1/3 of patients with DVT) 5) Cyanosis of the affected limb 6) Warmth on the affected limb
  22. 22. DIFFERENTIAL DIAGNOSES o Cellulitis (may coexist) o Ruptured Baker's cyst (both may coexist) - especially in individuals with pre- existing rheumatoid disease of the knee o Spontaneous/post-traumatic calf haematoma o Osteomyelitis o Pyomyositis o Pulmonary embolism o Thrombophlebitis superficial or septic o Lymphangitis o Varicose veins o Lymphedema o Achilles tendonitis o Arterial insufficiency o Asymptomatic peripheral edema secondary to CHF, Liver failure, renal failure or nephrotic syndrome.
  23. 23. INVESTIGATIONS 1) Imaging Studies a) Doppler U/S - Gold standard The flow of blood as detected by reflection of waves on rbcs is absent in DVT. b) Impedance Plethysmography Is based on recording changes in blood volume of an extremity, which are directly related to venous outflow. Standardized graphs are used to discriminate normal IPG study results from abnormal results. c) IV contrast Venography Is most definitive mtd of dx venous thrombosis bt 1-2% of patients develop phlebitis following procedure d) MRI Reserved for specific occasions which ultra-sound findings are equivocal or negative ultra-sound findings but strong clininical suspicion. e) CT-SCAN Requires contrast agents and ionizing radiation. DXT exposure to the foetus is negligible unless pelvic veins are imaged.
  24. 24. 2) Lab Studies D-dimer Blood test Are fibrin degradation products (FDP) D-dimer fibrin fragments are present in fresh fibrin clot and in fibrin degradation products or cross-linked fibrin.Monoclonal abs specific for the D-dimer fragment are used to differentiate fibirn-specific clot form non-cross linked fibrin and from fibrinogen. Thus has high sensitivity for venous thromboembolism. Low sensitivity
  25. 25. Treatment  Rationale  Prevent further clot extension  Prevention of acute pulmonary Embolism(PE) cos association with high mortality > 60%.  Reducing the risk of recurrent thrombosis  Limiting development of late complications e.g. postphlebitic syndrome, chronic venous insufficiency.
  26. 26. TREATMENT Consists of anti-coagulation, bed rest and analgesia. 1) Supportive management Consists of elevating the affected limb(s), serial measurements, elastic stockings and analgesia. Thus will alleviate the oedema and improve venous return & promote early ambulation. 2) Definitive management i.e. Anti-coagulation a) Heparin used in the Acute phase Can use either Unfractionated Heparin(UFH) or Low molecular weight heparin(LMWT) i)Using UFH, start with 10,000-15,000IU IV followed by contionous IV infusion of 10,000IU/ 4-6hrly. Aim is to make the APTT/KCCT 1.5-2X the control values UFH can also be used s.c @ 10,000-15,000IU tds. Heparin cannot cross the placenta due to its high molecular weight (16000-40000 daltons) Pharmacodynamics Anti-thrombin (an endogenous inhibitor of coagulation) inhibits clotting factor proteases by forming equimolar stable complexes with them. Heparin catalyzes the anti-thrombin-protease reaction without being consumed. Anti thrombin inhibits the intrinsic pathway{Factor IIa (Thrombin), Factor IXa (Christmas factor), Factor Xa (Stuart-Prower factor)} Heparin enhances Anti-Thrombin activity.
  27. 27. Pharmacokinetics of UFH Onset of action - 30mins T1 /2 - 1.5hrs Duration of action - 8hrs Adverse effects o Thrombocytopenia- is immune mediated and develops 6-10 days presenting with artertial thrombosis-White Clot syndrome. It results from irreversible aggregration of platelets induced by heparin o Osteoporosis-prolonged use o Hyper K+- inhibits aldosterone secretion o Hypersensitivity o Alopecia (rare) Antidote; Protamine sulphate 1mg/100U heparin IVI given within 15mins; Max dose; 50mg (if exceeded may itself have anticoagulant effect).
  28. 28. ii) LMWT heparin (enoxaparin (clexane®), dalteparin) o Inhibit FXa but have less effect on anti-thrombin & on coagulation in general o Convenient to use - SC OD/BD o Longer duration of action o Does not require monitoring o Reduce dose in renal insufficiency o Disadvantage is their high cost. b) Oral anticoagulation Warfarin- Coumarin derivative Is started once the acute phase is over and the APTT/KCCT IS 1.5-2X the control. Warfarin is continued for 3-4 days while on Heparin s.c. unitl the INR IS 2-3X the control then Heparin can be discontinued. Initial dose is 5mg od and is titrated to get an INR OF 2-3X the control Pharmacodynamics Blocks the γ-carboxylation of several glutamate residues in extrinsic pathway (Vitamin K dependent) factors II, VII, IX, & X as well as the endogenous anticoagulant protein C & S. The blockade results in incomplete molecules that are biologically inactive in coagulation.
  29. 29.  Warfarin is use in pregnancy:  Controversial cos associated teratogenicity.  Use after first trimester, convert patient back to Heparin at 36 weeks in preparation for labor to avoid bleeding- neonate and mother.  Instituted after delivery till end of puerperium. o Lifelong in recurrent DVT, proximal DVT Pharmacokinetics Onset of action - 48-72hrs T1 /2 - 36hrs Adverse effects o Hypercoagulability within the first few days of administration due to the rapid degradation of Protein C & S which have a short half life in plasma (2.5-3hrs) thus heparin is administered together with Warfarin for first 3-4 days.
  30. 30. Warfarin Antidote o Stop the drug and administer large doses of vitamin K1 (phytonadione) 10mg - takes 6-8hrs to take effect (disadvantage) & FFP or factor IX concentrates or cryoprecipitates o In emergencies, use fresh frozen plasma(FFP) or fresh blood.
  31. 31. warfarin embryopathy  Warfarin crosses placenta and has teratogenic potential.  There is convincing evidence that warfarin administration between the sixth and ninth weeks of gestation is potentially teratogenic  The most common developmental abnormalities affect bone and cartilage; causing chondromalacia punctata, with stippled epiphyses and nasal and limb hypoplasia
  32. 32. warfarin embryopathy  central nervous system (CNS) abnormalities (including optic atrophy, microcephaly, mental retardation, spasticity, and hypotonia)  Fetal or neonatal hemorrhage is a concern when warfarin is administered in the third trimesters.  So avoided in pregnancy when Heparin admnistration possible.  Avoid before week 14-16, convert to Heparin injection at 36 weeks as you await labor.
  33. 33. c) Other treatment modalities are; Venous thrombectomy still has a role in the management of patients with extensive iliofemoral disease in which limb loss is imminent IVC filters may be used in; o Active bleeding o When anti-coagulants fail o To minimize risk of PE during venous thrombectomy PROPHYLAXIS o Heparin 5000IU s.c. bd o Junior Aspirin 1 tablet od o Claxane (LMWT Heparin) 40 mg od s.c. PROGNOSIS All patients with proximal vein DVT are at long term risk of chronic venous innsufficiency. Approximately 20% of untreated proximal(above the calf) DVTs progress to pulmonary emboli, and 10-20% of these are fatal. With anti-coagulation therapy the mortality is decreased 5- to 10- fold.
  34. 34. COMPLICATIONS o Acute Pulmonary embolism o Systemic embolism o Chronic venous insufficiency o Post- phlebitic syndrome( i.e. pain and edema in the affected limb without new clot formation) o Soft tissue ischaemia associated with massive clot and very high venous pressures phlegmasia cerulea dolens PREVENTION o Avoid prolonged bed rest o Early ambulation following Surgery CONCLUSION DVT is a clinical condition which needs early diagnoses so as to reduce the incidence of pulmonary embolism and death.
  35. 35. Subsequent Pregnancies  Prophylactic anticoagulation.
  36. 36. THANK YOU

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