presentationaug2011

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59y old male with PMH of DM last Hba1c 6.2 in July , HTN, pulmonary HTN, OSA on CPAP, CKD (nephrotic syndrome) , CHF, EF: 67% presents with right leg swelling Vitals in ER T: 97.7 BP: 183/88 HR: 88 RR: 16 Sao2: 97% on room air

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DVT presentation

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Page 1: Presentationaug2011

59y old male with PMH of DM last Hba1c 6.2 in July , HTN, pulmonary HTN, OSA on CPAP, CKD (nephrotic syndrome) , CHF, EF: 67% presents with right leg swelling

Vitals in ER

T: 97.7BP: 183/88HR: 88RR: 16Sao2: 97% on room air

Page 2: Presentationaug2011

GE: well oriented to time ,place and person ,lying on the bed does not seem to be in acute distressCVS: S1, S2 RRR, No Murmurs, PMI not displacedLUNGS: Air movement equal bilaterally, No wheezes or creptitations, P/A: BS+ before palpation, soft, NT, ND, No rebound tenderness, no OM , CNS: A&OX 3, No focal deficit, gaits normal.EXT: No edema, pulses palpable., right leg: edema 2+ upto the knee, erythema and tender , no changes in left leg

Page 3: Presentationaug2011

Labs: Na: 140K: 4.6Cl: 106Co2: 29.9BUN: 35Crea: 2.2Ca: 8 .4Total protein: 6.2Albumin: 2.8Gfr:30Anion gap:4WBC: 8.0HGB: 15.0Platelets: 192MCV: 89.4RDW: 147APTT: 24.3PT: 11.0INR: 1.06

Page 4: Presentationaug2011

Venous ThromboembolismManagement

Namrata Dass

Page 5: Presentationaug2011

Diagnostic Testing

• D-dimer: positive test require further evaluation. (highly sensitive)

• negative D-dimer in combination with low pretest probability can exclude almost all PE

• Imaging• Compression ultrasound/duplex examination• May fail to visualize parts of the deep femoral

vein, parts of the upper extremity venous system, and the pelvic veins.

Page 6: Presentationaug2011

PE-specific testing

• Nondefinitive tests :ekg, troponin and brain natriuretic peptide (BNP) levels, blood gases

• Contrast-enhanced spiral (helical) chest CT:- Contraindications: renal dysfunction and dye allergy.- Advantages of CT scan over V/Q scan include more

diagnostic results , with fewer indeterminate or inadequate studies, and the detection of alternative diagnoses, such as dissecting aortic aneurysm, pneumonia, and malignancy.

Page 7: Presentationaug2011

V/Q scanning

• Classified as normal, non-diagnostic (i.e., very low probability, low probability, intermediate probability), or high probability for PE.

• Pulmonary angiography (PA) : gold standard

- Less invasive tests have mostly replaced PA over the past decade.

Page 8: Presentationaug2011

TREATMENT

• To prevent recurrent VTE,• To prevent consequences of VTE (i.e., post-

phlebitic syndrome [i.e., pain, edema, and ulceration], pulmonary arterial hypertension, and death), and

• To prevent complications of therapy (e.g., bleeding and HIT).

Page 9: Presentationaug2011

Medications

• WARFARIN: leads to depletion of the vitamin K-dependent clotting factors II, VII, IX, and X and proteins C, S, and Z.

• It requires 4 to 5 days to achieve the full anticoagulant effect.

• Because of the rapid depletion of the anticoagulant protein C and slower onset of anticoagulant effect, patients might develop increased hyper-coagulability if warfarin is not combined with a parenteral anticoagulant

Page 10: Presentationaug2011

• For most indications, warfarin has a target INR of 2.5 and a therapeutic range of 2 to 3.

• INR monitoring: twice weekly for 1 to 2 weeks, then weekly for 2 weeks, then less frequently.

• Unfractionated heparin (UFH): inactivation of thrombin and factor Xa by antithrombin.

• Prolongs both aPTT ,minimal effect on PT• For DVT prophylaxis, the typical dosage is

5,000 units SC q8-12h

Page 11: Presentationaug2011

• For therapeutic anticoagulation, UFH is usually administered IV with a bolus followed by continuous infusion

• Choice of anticoagulant in patient with increased risk of bleeding

Page 12: Presentationaug2011

LMWH

• Produced by chemical or enzymatic cleavage of UFH.• Minimally prolongs the aPTT.• In pt with renal dysfunction, obesity, or pregnancy,

factor Xa level monitoring may be prudent.• Because of the SC dosing route, LMWH facilitates

outpatient VTE therapy.• First choice in pregnant women and cancer pts

Page 13: Presentationaug2011

Fondaparinux

• Selective inhibitor of factor Xa.• Does not significantly prolong the aPTT.• Monitoring with factor X level not indicated

except in renal insufficiency• May be used for outpatient VTE therapy.

Page 14: Presentationaug2011

Lepirudin (Refludan, recombinant hirudin)

• Direct thrombin inhibitor that is used for the treatment of HIT

• Requires cautious use and dose adjustments in patients with renal insufficiency

• aPTT monitoring should occur 4 hours after a dose change

• Argatroban: used for HIT therapy.

Page 15: Presentationaug2011

Thrombolytic therapy

• Indications :refractory systemic hypotension and PE associated with objectively demonstrated (e.g. echocardiogram, spiral CT) acute, severe right ventricular strain

• alteplase or recombinant tissue plasminogen activator

Page 16: Presentationaug2011

IVC filters

• Indicated for acute DVT situations in which there are absolute contraindications to anticoagulation (e.g., active bleeding, severe thrombocytopenia, urgent surgery) or recurrent thromboemboli despite therapeutic anticoagulation.

Page 17: Presentationaug2011

• Surgical embolectomy should be considered in patients with life-threatening massive PE that have contraindications to thrombolytic therapy