Venous thromboembolism
Venous thromboembolism Microchapters |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]:Associate Editor(s)-in-Chief: Syed Hassan A. Kazmi BSc, MD [3]
Overiew
Classification
Venous thromboembolism (VTE) may be classified into:[1]
The following table further classifies DVT and PE:[2][3][4][5][4][6][7][8]
Classification of Venous thromboembolism | ||
---|---|---|
Clinical diagnosis | Sub-classification | Comments |
Deep vein thrombosis | Upper extremity |
|
Lower extremity |
| |
Pulmonary embolism (PE) | Massive PE (High risk) |
OR OR
|
Sub-massive PE (Intermediate risk PE) |
AND
| |
Low risk PE |
|
Epidemiology
Incidence
- The incidence of VTE increases with age, ranging from less than 5 cases per 100,000 people in childhood to 500 cases per 100,000 people in the elderly.[9]
- Subjects who are more than 65 years of age are at three times higher risk for VTE compared to those who are 45-54 years old.[10]
- In the United States, the annual incidence of VTE is estimated to be approximately 100 per 100,000 persons.[9]
Age
- The incidence of VTE increases with age, ranging from less than 5 cases per 100,000 people in childhood to 500 cases per 100,000 people in the elderly.[9]
- Subjects who are more than 65 years of age are at three times higher risk for VTE compared to those who are 45-54 years old.[10]
Gender
- Studies about differences in the incidence of VTE by gender have mixed results.
- In addition, the risk for DVT was reported to consistently increase with age across both genders.[10]
Race
- There is a significant difference in the incidence of DVT as it relates to race. African Americans characteristically have the highest incidence of DVT while Caucasians rank as the second highest incidence of DVT.[9]
- When compared to African Americans and Caucasians, the incidence of DVT is noted to be two to four times lower in Hispanics and Asian-Pacific Islanders.[9]
- Lower incidence of thrombosis in non-Caucasians may be related to a lower prevalence of disorders like Factor V Leiden or Prothrombin 20210A mutation.[14][15]
Hospitalization for VTE
- During 2007–2009, an estimated annual average of 547,596 hospitalizations had a diagnosis of VTE for adults aged ≥18 years. Estimates for DVT and PE diagnoses were not mutually exclusive. An estimated annual average of 348,558 adult hospitalizations had a diagnosis of DVT, and 277,549 adult hospitalizations had a diagnosis of PE. An estimated annual average of 78,511 adult hospitalizations (14% of overall VTE hospitalizations) had diagnoses of both DVT and PE.[16]
- The estimated average annual number of hospitalizations with VTE was successively greater among older age groups: 54,034 for persons aged 18–39 years; 143,354 for persons aged 40–59 years; and 350,208 for persons aged ≥60 years. The estimated average annual number of hospitalizations with VTE was comparable for men (250,973) and women (296,623).[16]
- Shown below is an image depicting the estimated average annual number of hospitalization with a diagnosis of DVT, PE, or VTE by age and sex.
- The average annual rates of hospitalizations with a discharge diagnosis of DVT, PE, or VTE among adults were 152, 121, and 239 per 100,000 population, respectively. For VTE, the average annual rates were 60 per 100,000 population aged 18–39 years, 143 for persons aged 40–49 years, 200 for persons aged 50–59 years, 391 for persons aged 60–69 years, 727 for persons aged 70–79 years, and 1,134 for persons aged ≥80 years. The rates of hospitalization were similar for men and women, and the point estimates increased for both sexes by age.[16]
- On average, 28,726 hospitalized adults with a VTE diagnosis died each year. Of these patients, an average of 13,164 had a DVT diagnosis and 19,297 had a PE diagnosis; 3,735 had both DVT and PE diagnoses.[16]
Recurrence of VTE
- The risk of recurrence of VTE in patients diagnosed with first-time VTE is estimated to be around 7-8 percent per year during an average follow up period of 2.2 years of subsequent observation of 265 patients.[10]
- Among patients with a first episode of VTE, the risk of recurrence of VTE is particularly elevated in the first 6 to 12 months following the first episode of VTE. The risk of recurrent VTE remains up to 10 years, with a estimated cumulative incidence of first overall VTE recurrence of 30 %. Predictors for recurrence of VTE include malignancy, neurological diseases, and paresis.[19]
- In recent years, the increase in thrombosis incidence may be related to improved diagnostic modalities and increased awareness by clinicians.[9]
Complications of VTE
- Estimates suggest that 60,000-100,000 Americans die of VTE, 10 to 30% of which will die within one month of diagnosis.[17][18]
- Among people who have had a DVT, one-half will have long-term complications (post-thrombotic syndrome) such as swelling, pain, discoloration, and scaling in the affected limb.[17][18]
Risk Factors
Shown below is a list of predisposing factors for VTE.[20][21] The risk factors are classified as moderate or weak depending on how strongly they predispose for a VTE.
Moderate risk factors | Weak risk factors |
---|---|
❑ Chemotherapy ❑ Obesity ❑ Chronic heart failure |
❑ Advanced age ❑ Laparoscopic surgery |
Risk factors of VTE may be categorized in to modifiable, non-modifiable, temporary and other risk factors.
Modifiable Risk Factors | Non-Modifiable Risk Factors | Temporary Risk Factors | Other Risk Factors |
❑ Modifiable risk factors are reversible based upon lifestyle/behavior modification. |
❑ Advanced age
|
❑ Pregnancy and the peri-partum period |
❑ Other possible factors associated with VTE include:[27]
|
Diagnosis
Suspected pulmonary embolism | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
D-dimer | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
Negative | Positive | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stop | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
CXR | Ultrasound If signs of DVT present | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Normal PE unlikely with positive D-dimer or PE likely | Abnormal PE unlikely with positive D-dimer or PE likely | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
V/Q scan | CTPA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Nnormal | Non diagnostic | High probability | PE present | PE absent | |||||||||||||||||||||||||||||||||||||||||||||||||||
Stop | Treat | Treat | Stop | ||||||||||||||||||||||||||||||||||||||||||||||||||||
PE unlikely | PE likely | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Serial ultrasound | CTPA or serial ultrasound | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Treatment
Prevention
Patient population | Sub-population | Scoring criteria for risk assessment | Major predisposing risk factors and their score | Prophylaxis recommendations | ||||
---|---|---|---|---|---|---|---|---|
Padua score
(Score≥ 4: High risk for VTE Score< 4: Low risk for VTE) |
IMPROVE score (0 0.5%
1 1.0% 2 1.7% 3 3.1% 4 5.4% 5-8 11%) |
IMPROVE bleeding risk score
(Score ≥7: Elevated risk of bleeding Score <7: Not elevated risk of bleeding) |
IMPROVE Associative score
(Score 0-1: Low risk for VTE Score 2-3: Intermediate risk for VTE Score 4-10: Hight risk for VTE) |
Caprini score
(Score 0-1: Low risk of VTE Score 2: Moderate of VTE Score 3-4: High risk of VTE Score ≥ 5: Highest risk for VTE) | ||||
Non-surgical patients | Acutely ill patients | ✔ | ✔ | ✔ | - | - | IMPROVE:
|
|
IMPROVE bleeding risk:
|
||||||||
Cancer in outpatient |
AND
|
|||||||
Chronically immobilized patients | - | - | - | - | - | - | Not indicated | |
Long travel |
|
|||||||
Asymptomatic thrombophilia | - | - | - | - | - | - | Not indicated | |
Surgical patients | Orthopedic surgery patients | |||||||
General and abdominal pelvic surgeries | - | - | - | - | ✔ | Caprini:
|
||
Cardiac surgery | - | - | - | - | ✔ | |||
Thoracic surgery | - | - | - | - | ✔ | |||
Craniotomy | - | - | - | - | ✔ | |||
Spinal surgery | - | - | - | - | ✔ | |||
Trauma | - | - | - | - | ✔ |
Non-surgical patients
(i) Prevention in acutely ill hospitalized patients
Risk assessment in acutely ill patients
The following scoring systems can be used to assess the risk of VTE, based on risk factors:
(a) Padua prediction score for VTE
Shown below is a table depicting Padua predictive score for VTE among hospitalized medical patients. The interpretation of the score is as follows:
- Score≥ 4: High risk for VTE
- Score< 4: Low risk for VTE[28]
Variable | Score |
---|---|
Active cancer | 3 |
Previous VTE | 3 |
Decreased mobility | 3 |
Thrombophilia | 3 |
Previous trauma or surgery within that last month | 2 |
Age≥ 70 | 1 |
Heart and/or respiratory failure | 1 |
Ischemic stroke or acute myocardial infarction | 1 |
Acute rheumatologic disorder and/or acute infection | 1 |
Obesity | 1 |
Hormonal therapy | 1 |
(b) IMPROVE predictive score for VTE
Calculation of the IMPROVE predictive score
Variable | Score[29] |
---|---|
Prior episode of VTE | 3 |
Thrombophilia | 3 |
Malignancy | 1 |
Age more than 60 years | 1 |
Interpretation of the IMPROVE predictive score
Score | Predicted VTE risk through 3 months[29] |
---|---|
0 | 0.5% |
1 | 1.0% |
2 | 1.7% |
3 | 3.1% |
4 | 5.4% |
5-8 | 11% |
(ii) Preventive approach in acutely ill hospitalized patients based on risk assessment
Abbreviations: LDUH: low dose unfractionated heparin; LMWH: low molecular weight heparin; VTE: Venous thromboembolism
What is the risk of thrombosis in the acutely ill patient? | |||||||||||||||||||||||
High | Low | ||||||||||||||||||||||
Is the patient bleeding or at high risk of bleeding? | No VTE prophylaxis | ||||||||||||||||||||||
Yes | No | ||||||||||||||||||||||
Mechanical VTE prophylaxis For the period of immobilization or hospital stay only ❑ Graduated compression stocking ❑ Intermittent pneumatic compression | Pharmacological VTE prophylaxis For the period of immobilization or hospital stay only ❑ LMWH ❑ LDUH, BID ❑ LDUH, TID ❑ Fondaparinux | ||||||||||||||||||||||
Did the bleeding or bleeding risk subside AND the patient is still at increased risk of thrombosis? | |||||||||||||||||||||||
Yes | No | ||||||||||||||||||||||
❑ Substitute mechanical prophylaxis by pharmacological prophylaxis | ❑ Continue mechanical prophylaxis | ||||||||||||||||||||||
(iii) Prevention in critically ill hospitalized patients
Risk assessment in critically ill patients
(a) IMPROVE bleeding risk score
Shown below is a table depicting the IMPROVE risk score for bleeding among hospitalized medical patients. The scores can be interpreted as such:[30]
- Score ≥7: Elevated risk of bleeding
- Score <7: Not elevated risk of bleeding
Variable | Score |
---|---|
Active gastric or duodenal ulcer | 4.5 |
Prior bleeding within the last 3 months | 4 |
Thrombocytopenia (<50x109/L) | 4 |
Age ≥ 85 years | 3.5 |
Liver failure (INR>1.5) | 2.5 |
Severe kidney failure (GFR< 30 mL/min/m2) | 2.5 |
Admission to ICU or CCU | 2.5 |
Central venous catheter | 2 |
Rheumatic disease | 2 |
Active malignancy | 2 |
Age: 40-84 years | 1.5 |
Male | 1 |
Moderate kidney failure (GFR: 30-59 mL/min/m2) | 1 |
(iv) Preventive approach in critically ill hospitalized patients
Abbreviations: LDUH: low dose unfractionated heparin; LMWH: low molecular weight heparin; VTE: Venous thromboembolism
Is the critically ill patient bleeding or at risk for major bleeding? | |||||||||||||||||
Yes | No | ||||||||||||||||
Mechanical VTE prophylaxis | Pharmacological VTE prophylaxis | ||||||||||||||||
Did the bleeding or bleeding risk subside? | |||||||||||||||||
Yes | No | ||||||||||||||||
❑ Substitute mechanical prophylaxis by pharmacological prophylaxis | ❑ Continue mechanical prophylaxis | ||||||||||||||||
Shown below is an algorithm depicting VTE prophylaxis among cancer patients. Note that, cancer patients with indwelling central venous catheters do not require VTE prophylaxis with neither low molecular weight heparin, low dose unfractionated heparin or vitamin K antagonists.[31]
Abbreviations: LDUH: low dose unfractionated heparin; LMWH: low molecular weight heparin; VTE: Venous thromboembolism
❑ Does the patient have a solid tumor AND ❑ Additional risk factors for VTE?
| |||||||||||||||
Yes | No | ||||||||||||||
Pharmacological VTE prophylaxis | ❑ No VTE prophylaxis | ||||||||||||||
- ↑ Moheimani F, Jackson DE (2011). "Venous thromboembolism: classification, risk factors, diagnosis, and management". ISRN Hematol. 2011: 124610. doi:10.5402/2011/124610. PMC 3196154. PMID 22084692.
- ↑ Anand SS, Wells PS, Hunt D, Brill-Edwards P, Cook D, Ginsberg JS (1998). "Does this patient have deep vein thrombosis?". JAMA. 279 (14): 1094–9. PMID 9546569. Unknown parameter
|month=
ignored (help) - ↑ Wells PS, Hirsh J, Anderson DR; et al. (1995). "Accuracy of clinical assessment of deep-vein thrombosis". Lancet. 345 (8961): 1326–30. PMID 7752753. Unknown parameter
|month=
ignored (help) - ↑ 4.0 4.1 Cogo A, Lensing AW, Prandoni P, Hirsh J (1993). "Distribution of thrombosis in patients with symptomatic deep vein thrombosis. Implications for simplifying the diagnostic process with compression ultrasound". Arch. Intern. Med. 153 (24): 2777–80. PMID 8257253. Unknown parameter
|month=
ignored (help) - ↑ Galanaud JP, Sevestre-Pietri MA, Bosson JL, Laroche JP, Righini M, Brisot D, Boge G, van Kien AK, Gattolliat O, Bettarel-Binon C, Gris JC, Genty C, Quere I (2009). "Comparative study on risk factors and early outcome of symptomatic distal versus proximal deep vein thrombosis: results from the OPTIMEV study". Thromb. Haemost. 102 (3): 493–500. doi:10.1160/TH09-01-0053. PMID 19718469. Retrieved 2011-12-14. Unknown parameter
|month=
ignored (help) - ↑ Joffe HV, Kucher N, Tapson VF, Goldhaber SZ (2004). "Upper-extremity deep vein thrombosis: a prospective registry of 592 patients". Circulation. 110 (12): 1605–11. doi:10.1161/01.CIR.0000142289.94369.D7. PMID 15353493. Retrieved 2012-10-07. Unknown parameter
|month=
ignored (help) - ↑ Isma N, Svensson PJ, Gottsäter A, Lindblad B (2010). "Upper extremity deep venous thrombosis in the population-based Malmö thrombophilia study (MATS). Epidemiology, risk factors, recurrence risk, and mortality". Thromb Res. 125 (6): e335–8. doi:10.1016/j.thromres.2010.03.005. PMID 20406709.
- ↑ Muñoz FJ, Mismetti P, Poggio R, Valle R, Barrón M, Guil M; et al. (2008). "Clinical outcome of patients with upper-extremity deep vein thrombosis: results from the RIETE Registry". Chest. 133 (1): 143–8. doi:10.1378/chest.07-1432. PMID 17925416.
- ↑ 9.0 9.1 9.2 9.3 9.4 9.5 White RH (2003). "The epidemiology of venous thromboembolism". Circulation. 107 (23 Suppl 1): I4–8. doi:10.1161/01.CIR.0000078468.11849.66. PMID 12814979.
- ↑ 10.0 10.1 10.2 10.3 10.4 Cushman M, Tsai AW, White RH, Heckbert SR, Rosamond WD, Enright P; et al. (2004). "Deep vein thrombosis and pulmonary embolism in two cohorts: the longitudinal investigation of thromboembolism etiology". Am J Med. 117 (1): 19–25. doi:10.1016/j.amjmed.2004.01.018. PMID 15210384.
- ↑ Silverstein MD, Heit JA, Mohr DN, Petterson TM, O'Fallon WM, Melton LJ (1998). "Trends in the incidence of deep vein thrombosis and pulmonary embolism: a 25-year population-based study". Arch Intern Med. 158 (6): 585–93. PMID 9521222.
- ↑ Kniffin WD, Baron JA, Barrett J, Birkmeyer JD, Anderson FA (1994). "The epidemiology of diagnosed pulmonary embolism and deep venous thrombosis in the elderly". Arch Intern Med. 154 (8): 861–6. PMID 8154949.
- ↑ "Venous Thromboembolism in Adult Hospitalizations — United States, 2007–2009". Retrieved 2012-10-06.
- ↑ Ridker PM, Miletich JP, Hennekens CH, Buring JE (1997). "Ethnic distribution of factor V Leiden in 4047 men and women. Implications for venous thromboembolism screening". JAMA. 277 (16): 1305–7. PMID 9109469.
- ↑ Gregg JP, Yamane AJ, Grody WW (1997). "Prevalence of the factor V-Leiden mutation in four distinct American ethnic populations". Am J Med Genet. 73 (3): 334–6. PMID 9415695.
- ↑ 16.0 16.1 16.2 16.3 [1] Hussain R. Yusuf, MD, James Tsai, MD, Hani K. Atrash, MD, Sheree Boulet, DrPH, Scott D. Grosse, PhD, Div of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, CDC. Venous Thromboembolism in Adult Hospitalizations — United States, 2007–2009
- ↑ 17.0 17.1 17.2 Beckman MG, Hooper WC, Critchley SE, Ortel TL (2010). "Venous thromboembolism: a public health concern". Am J Prev Med. 38 (4 Suppl): S495–501. doi:10.1016/j.amepre.2009.12.017. PMID 20331949.
- ↑ 18.0 18.1 18.2 CDC- Deep Vein Thrombosis (DVT) / Pulmonary Embolism (PE) — Blood Clot Forming in a Vein
- ↑ Heit JA, Mohr DN, Silverstein MD, Petterson TM, O'Fallon WM, Melton LJ (2000). "Predictors of recurrence after deep vein thrombosis and pulmonary embolism: a population-based cohort study". Arch Intern Med. 160 (6): 761–8. PMID 10737275.
- ↑ Anderson FA, Spencer FA (2003). "Risk factors for venous thromboembolism". Circulation. 107 (23 Suppl 1): I9–16. doi:10.1161/01.CIR.0000078469.07362.E6. PMID 12814980.
- ↑ Torbicki A, Perrier A, Konstantinides S, Agnelli G, Galiè N, Pruszczyk P; et al. (2008). "Guidelines on the diagnosis and management of acute pulmonary embolism: the Task Force for the Diagnosis and Management of Acute Pulmonary Embolism of the European Society of Cardiology (ESC)". Eur Heart J. 29 (18): 2276–315. doi:10.1093/eurheartj/ehn310. PMID 18757870.
- ↑ 22.0 22.1 Holst AG, Jensen G, Prescott E (2010). "Risk factors for venous thromboembolism: results from the Copenhagen City Heart Study". Circulation. 121 (17): 1896–903. doi:10.1161/CIRCULATIONAHA.109.921460. PMID 20404252.
- ↑ Vayá A, Martínez-Triguero ML, España F, Todolí JA, Bonet E, Corella D (2011). "The metabolic syndrome and its individual components: its association with venous thromboembolism in a Mediterranean population". Metab Syndr Relat Disord. 9 (3): 197–201. doi:10.1089/met.2010.0117. PMID 21352080.
- ↑ Eichinger S, Hron G, Bialonczyk C, Hirschl M, Minar E, Wagner O; et al. (2008). "Overweight, obesity, and the risk of recurrent venous thromboembolism". Arch Intern Med. 168 (15): 1678–83. doi:10.1001/archinte.168.15.1678. PMID 18695082.
- ↑ Pomp ER, Rosendaal FR, Doggen CJ (2008). "Smoking increases the risk of venous thrombosis and acts synergistically with oral contraceptive use". Am J Hematol. 83 (2): 97–102. doi:10.1002/ajh.21059. PMID 17726684.
- ↑ den Heijer M, Koster T, Blom HJ, Bos GM, Briet E, Reitsma PH; et al. (1996). "Hyperhomocysteinemia as a risk factor for deep-vein thrombosis". N Engl J Med. 334 (12): 759–62. doi:10.1056/NEJM199603213341203. PMID 8592549.
- ↑ Konofal E, Lecendreux M, Cortese S (2010). "Sleep and ADHD". Sleep Med. 11 (7): 652–8. doi:10.1016/j.sleep.2010.02.012. PMID 20620109.
- ↑ Barbar S, Noventa F, Rossetto V, Ferrari A, Brandolin B, Perlati M; et al. (2010). "A risk assessment model for the identification of hospitalized medical patients at risk for venous thromboembolism: the Padua Prediction Score". J Thromb Haemost. 8 (11): 2450–7. doi:10.1111/j.1538-7836.2010.04044.x. PMID 20738765.
- ↑ 29.0 29.1 Spyropoulos AC, Anderson FA, Fitzgerald G, Decousus H, Pini M, Chong BH; et al. (2011). "Predictive and associative models to identify hospitalized medical patients at risk for VTE". Chest. 140 (3): 706–14. doi:10.1378/chest.10-1944. PMID 21436241.
- ↑ Decousus H, Tapson VF, Bergmann JF, Chong BH, Froehlich JB, Kakkar AK; et al. (2011). "Factors at admission associated with bleeding risk in medical patients: findings from the IMPROVE investigators". Chest. 139 (1): 69–79. doi:10.1378/chest.09-3081. PMID 20453069.
- ↑ Kahn SR, Lim W, Dunn AS, Cushman M, Dentali F, Akl EA; et al. (2012). "Prevention of VTE in nonsurgical patients: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines". Chest. 141 (2 Suppl): e195S–226S. doi:10.1378/chest.11-2296. PMC 3278052. PMID 22315261.