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VENOUS THROMBOEMBOLIC DISEASE R. Duncan Hite, MD Section on Pulmonary and Critical Care Medicine

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VENOUS THROMBOEMBOLIC DISEASE

R. Duncan Hite, MDSection on Pulmonary and Critical Care Medicine

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Venous Thromboembolic Disease

• Venous thrombosis - ~ 5 million pts yearly• Most caused by inadequate prophylaxis in hospitalized pts

• 10 % suffer pulmonary embolism ~ 500,000• ~ 1% of all hospitalized pts have PE• Contributes to 6 % of all hospital deaths• ~ 125,000 deaths annually from PE

• 3rd most common cardiovascular cause of death (MI, CVA)

• Most deaths occur early – PREVENTION IS KEY!!

• Diagnosis of PE made in < 30% when contributes to death; < 10% if incidental

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CASE 1

• July 8 - 37 yo WM presents to the ED with right sided pleuritic chest pain x 24 hours. No fever or cough. Minimal SOB. Denies chest trauma.

• PMH: bronchitis/sinusitis, Multiple Sclerosis x 5 years (uses cane, + muscle spasms - Rx’d Baclofen), Smoker• Exam: HR 107, BP 124/82, SaO2 93% (RA), Afeb, tenderness over R ribs, coarse breath sounds on R, normal LE’s.• Tests: Nml CBC, CXR w/ “vague” infiltrate in RUL

• Dx: Costochondritis - Rx’d with NSAIDs• July 10 - F/U w/PCP - Dx’ed with pneumonia - Rx’d w/Biaxin• July 12 - returns to ED with presyncope, N/V - D/C’d home

- returns 2 hours later with PEA arrest and dies - autopsy -- massive PE

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CASE 2

• Early June - 52 yo BM admitted for acute AMI requiring cardiac cath and PTCA of LAD. Requires mechanical ventilation x 5 days, ICU x 7 days and in hospital x 10 days. ECHO prior to d/c reveals EF of approx 25%. • Late June - pt readmitted for W/U of persistent leukocytosis noted on earlier admission. Undergoes BM Bx with findings consistent with CML. Discharged to home after 3 days.• Early July (5 days post d/c) - Seen in walk-in clinic for non-productive cough and SOB. CXR clear. Dx: bronchitis • Mid July - symptoms persist/worse. Repeat CXR reveals new LLL effusion. Dx’ed with CHF and given diuretics. + PPD.• Early August - referred to Pulmonary Clinic for persistent cough, SOB and effusion. ? CA v. TB.

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CASE 3

- 43 yo AA male truck driver who has bilateral knee injuries while playing basketball. Requires bilateral knee repairs requiring fixation of both lower extremities for 6 - 8 weeks. Received appropriate DVT prophylaxis during hospital stay.

- Returns to the ED 4 weeks later with chest pain, SOB and hypoxemia. Has massive PE by CT angiogram and pulmonary hypertension/RV dilation by echocardiogram.

- Given TPA with good clinical response.

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Venous Thromboembolic DiseaseEpidemiology

• 85-90% of PE pts have DVT risk factors

• 90-95% of PEs arise from lower ext. DVT

• Defined DVT Risk Factors: (Virchow’s Triad)– Venous stasis - CHF, Immobility, Age > 70, Travel, Obesity,

Recent surgery (4 weeks) or hospitalization (6 mos)

– Venous Injury - Prior DVT/PE, LE Trauma/Surgery– LE trauma or surgery - Very high (50+%)– Major surgery - (5 - 8%)

– Hypercoaguability - Cancer, Pregnancy, Nephrotic Syndrome, Hyperhomocysteinemia, Factor V Leyden mutation, Deficiency of Protein C/S or ATIII, Anti Phospholipid Ab, HITTS, Smoking

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Deep Venous ThrombosisDiagnosis

• Venography - remains the “gold standard”• Pitfalls: Difficult to perform, expensive, contrast load, DVT

• Compression Ultrasound (Sonography, Duplex and Color Doppler)• Criteria: echogenicity, noncompressibility, distension, free floating

thrombus, absence of Doppler waveform, Abnormal color image

• Accuracy:– Symptomatic Patients: Sensitivity = 90-100%, Specificity = 95-100%

– High Risk Asymptomatic: Sensitivity = 50-80%, Specificity = 95-100%

• Impedance Plethysmography

• Radionuclide Venography (Indium-111)

• MRI - increasing popularity and utilization, includes deep pelvic veins

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Deep Venous ThrombosisPrevention

• ACCP Consensus Guidelines Chest, 2004, 126 (3), Sept Supplement

Includes:Prevention of venous thromboembolismAntithrombotic therapy for venous

thrombo-embolic diseaseAntithrombotic therapy for:

Afib, MI, CVA, Valvular Heart Do, PVD

Heparin-induced thrombocytopenia

Anticoagulants

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Deep Venous ThrombosisPrevention

• Orthopedic Surgery

• Other Surgery (General, Urologic, Vascular, Gyn)

• Neurosurgery

• Trauma, Spinal Cord Injury, Burns

• Medical (General, Cancer, Critical Care)

• Long Distance Travel

ACCP Consensus Statement. Chest, 2004, 126 (3), Sept suppl.

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Deep Venous ThrombosisPrevention

Samama, etal Samama, etal NEJMNEJM, 1999, 341, , 1999, 341, 793.793.

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Deep Venous ThrombosisPrevention

Samama, etal Samama, etal NEJMNEJM, 1999, 341, , 1999, 341, 793.793.

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Deep Venous ThrombosisPrevention

Samama, etal Samama, etal NEJMNEJM, , 1999, 341, 793.1999, 341, 793.

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PE SIGNS AND SYMPTOMS

Symptoms• Dyspnea - 80%• Chest pain - 70%• Cough - 50%• Apprehension - 50%• Hemoptysis - 30%

Signs• Tachycardia - 60%• Tachypnea - 70%• Fever - 60%• Clinical DVT - 30%

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Pulmonary Embolism Diagnosis

• Chest x-ray - nonspecific abnormalities in most; normal early

• Westermark's sign and Hampton's hump uncommon

• Arterial blood gas – hypoxemia is common• 15 - 20% will not manifest hypoxemia (i.e. normal A-a

gradient)

• ECG – nonspecific changes typically• S1Q3T3 pattern in massive PE with RV strain

• helpful in evaluating other causes of chest pain

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PE – V/Q LUNG SCAN

• Radiolabeled Xenon inhaled for ventilation and radiolabeled Technetium for perfusion

• Safe• Not very specific• Not very useful if pre-

existing lung disease

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Pulmonary EmbolismDiagnosis - V/Q Scan

CLINICAL PROBABILITY Scan Prob High Intermed. Low

High 96%(28/29)

88%(70/80)

56%(5/9)

Int./Ind. 66%(27/41)

28%(66/236)

16%(11/68)

Low 40%(6/15)

16%(30/191)

4%(4/90)

Normal 0%(0/5)

6%(4/62)

2%(1/61)

PIOPED. JAMA, 1990, 263, 2753.

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Pulmonary EmbolismClinical Presentation: D-dimer

Pts w/ PE Pts w/o PEPre-TestProbability

+ D-dimer - D-dimer + D-dimer - D-dimer

Low 19 5 163 516

Moderate 81 20 136 145

High 67 5 11 9

Ginsberg, Ann Int Med, 1998, 129, 1006.

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Pulmonary EmbolismClinical Presentation: D-dimer

Pts w/ PE Pts w/o PELungScan + D-dimer - D-dimer + D-dimer - D-dimer

Normal 3 1 73 242

Indeterminate 40 12 227 419

High Prob 124 17 10 9

Ginsberg, Ann Int Med, 1998, 129, 1006.

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Pulmonary EmbolismProbability Assessment

Ginsberg, Ann Int Med, 1998, 129, 1006.

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Pulmonary EmbolismProbability Assessment

Anand, Wells, etal. JAMA, 1998, 279, 1094.

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Pulmonary EmbolismProbability Assessment

Anand, Wells, etal. Ann Int Med, 2005, 143, 129.

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Pulmonary EmbolismDiagnosis - Chest CT

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• Accurate for segmental or larger PE• Sensitivity 85 - 95% (Overall 50-60%)

• Specificity 90 - 100%

• Accuracy depends on interpreter• Large Inter-interpreter variability

• Reduced accuracy with less experience

• Significant contrast load ~ 65% of PA gram• Similar expense to Pulmonary Arteriogram• Can identify other pulmonary etiologies

Pulmonary EmbolismDiagnosis - Chest CT

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Pulmonary EmbolismDiagnosis - Pulmonary Arteriogram

• Remains “gold standard” for Dx of PE• Expensive• Low morbidity and mortality

– Mortality < 0.1%

– Major morbidity < 0.5%

– Pulmonary Hypertension not a contraindication

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Pulmonary EmbolismDiagnosis - Pulmonary Arteriogram

Lobar DefectNormal Segmental Defect

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Pulmonary Emboli Diagnosis - MRA

AngiogramMRA

PE + PE - Total

PE + 27 2 29

PE - 8 81 89

Total 35 83 118

Oudkerk, etal. Lancet, 2002, 359, 1643.

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Venous ThromboembolismTreatment

Continuous IV Heparin:– Begin when PE suspected - bolus dose

– Continue for 7 - 10 days overlap with warfarin

– Permits fibrinolytic system (plasmin) to lyse clot

– Inhibits further clot formation / propagation

– Give adequate dose!• Recurrence higher with lower doses

• Weight based bolus with “protocol” for adjustments

– Emphasis on PTT probably excessive• PTT not direct measure of antithrombotic effect

• PTT does not correlate with bleeding complications

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Venous ThromboembolismTreatment

Low Molecular Weight Heparins:– Dosing: (Lovenox)

• Prophylaxis: 30 mg BID• Treatment: 1 mg/kg twice daily or 1.5 mg/kg

qday (max 150 mg)

– Less monitoring (Factor Xa assay)• Two Exceptions:

– Obesity– Renal Failure

– Cross Reactive with Heparin Antibodies• Less immunogenic if used primarily

Molecular weight (daltons)

10,000 15,0005,000

5,400

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Heparin-Induced AntibodiesHITTS

• Clinicopathologic Syndrome:

• Unexplained 50% decrease in platelets (even if absolute total > 150)

• Positive test for Heparin antibodies• Activation assay (more relevant but more difficult)• Antigen assay

• Types:• Type I

• begins early (few hours) after starting heparin• typically benign with plts usually staying > 100K. No Rx needed.

• Type II• begins several days into treatment (unless previously sensitized)• High risk for thrombotic complications. Requires Rx.

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Venous ThromboembolismOutpatient LMWH

Enoxaparin sodium

Unfractionated heparin

$2,278

$5,323

To

tal

mea

n c

ost

s p

er p

atie

nt

(CA

N)

P 0.0001

95% CI $2,012 to $4,050

O’Brien et al. O’Brien et al. Arch Int MedArch Int Med. . 1999;159:2298-2304.1999;159:2298-2304.

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Venous ThromboembolismTreatment

Synthetic Heparins:Fondaparinux (Arixtra)– Trials:

• DVT Prevention in Orthopedic Surgery Lancet, 2002, 359,

1715-26

– Dosing:• Prophylaxis: 2.5 mg qday

– Less monitoring (Factor Xa assay)• Not recommended in renal failure

– Does not cause Heparin Antibodies (??)

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Venous ThromboembolismTreatment

Oral anticoagulation (Coumadin):– Inhibits synthesis of Vitamin K dependent factors

• PT sensitive to Factor VII - short half-life -correlates with bleeding risk

• Thrombosis related to Factors II and X - longer half-life

– Overlap with heparin or LMWH until PT therapeutic for 3 - 5 days

• Coumadin decreases Protein C and S levels more quickly

– Warfarin load (high dose) not useful– Target INR range = 2.0 - 3.0– Continue anticoagulation for 3 months to lifetime

depending on # events and risk factors.

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Venous ThromboembolismTreatment - Thrombolytics

• Massive Pulmonary Embolism• Significant hemodynamic compromise present

• Evidence of RV failure on Echocardiogram (?)

• Phlegmasia Cerulea Dolens

• Agents studied• Streptokinase - 250,000 U load; 100,000 U/hr x 24hrs

• Urokinase - 4,400 U load; 2,200 U/hr x 12 hrs

• tPA - 100mg over 2 hrs

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Pulmonary Hypertension Hemodynamic Effects

PAP PVR

RV/RA CO RVEDV

LVEDV CO HR

BP SVR

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Pulmonary EmbolismTreatment - Thrombolytics

Konstantinides, etal. N Engl J Med, 2002, 347, 1143.

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Inferior Vena Cava Filter

• Indications:

• Intolerance to anticoagulation**

• Recurrent PE despite adequate anticoagulation

• Chronic PE with Pulm HTN

• Surgical removal of acute or chronic PE

• Massive PE (?)

• Outcomes:

• PE rate, DVT rate, Mortality unchanged

• Decousos, etal. (NEJM, 1998, 338, 409) - no benefit• Pts with contraindication/failure of anticoagulation excluded

• CONTINUE ANTICOAGULATION! - if possible

Ballew etal. Clin Chest Med, 1995, 16, 295.

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