User:4W7H13D/Thromboembolism
Thromboembolism is a condition in which a blood clot (thrombus) breaks off from its original site and travels through the bloodstream (as an embolus) to obstruct a blood vessel, causing tissue ischemia and organ damage. Thromboembolism can affect both the venous and arterial systems, with different clinical manifestations and management strategies.[1]
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[edit]Thromboembolism is a condition in which a blood clot (thrombus) breaks off from its original site and travels through the bloodstream to obstruct a blood vessel. This can cause tissue ischemia and organ damage. Thromboembolism can affect both the venous and arterial systems, with different clinical manifestations and management strategies for each.[1][2]
Article body
[edit]Venous thromboembolism
[edit]Main articles: Deep vein thrombosis and Pulmonary embolism
Venous thromboembolism (VTE) BD72 comprises the following conditions:[2][3][4]
- deep vein thrombosis (DVT) [2][3][4] BD71,
- pulmonary embolism (PE) [2][3][4] BB00.
VTE is a common cardiovascular disorder with significant morbidity and mortality [2][3][4].
Signs and Symptoms
[edit]VTE can present with various symptoms, such as painful leg swelling, chest pain, dyspnea, hemoptysis, syncope, and even death, depending on the location and extent of the thrombus.[3][5] VTE can also cause long-term complications, such as recurrent VTE, post-PE syndrome, chronic thromboembolic pulmonary hypertension (CTEPH), and post-thrombotic syndrome (PTS).
Treatment
[edit]The mainstay of VTE management is anticoagulation therapy, which prevents thrombus propagation and embolization. Such treatment reduces the risk of recurrence.[6][3][4] The choice and duration of anticoagulation depend on the individual patient's risk factors, bleeding risk, and preferences.
Direct oral anticoagulants (DOACs) have emerged as an essential alternative to conventional anticoagulants, such as vitamin K antagonists (VKAs) and low-molecular-weight heparins (LMWHs), due to their rapid onset of action, predictable pharmacokinetics, fixed dosing, and lower risk of bleeding. DOACs can also facilitate home treatment and extended therapy for selected patients.
In addition to anticoagulation, some patients with VTE may benefit from adjunctive therapies, such as thrombolysis, catheter-directed interventions, or inferior vena cava (IVC) filters, to remove or prevent thrombus migration. However, these therapies are associated with higher risks of bleeding and complications. These therapies are not routinely recommended by the current guidelines except for specific indications, such as massive PE, iliofemoral DVT, or contraindications to anticoagulation.
The optimal duration of anticoagulation for VTE is determined by the balance between the risk of recurrence and the risk of bleeding, and should be individualized for each patient. In general, VTE provoked by a transient or reversible risk factor, such as surgery, trauma, or immobilization, should be treated for three months, while VTE provoked by a persistent or progressive risk factor, such as cancer, should be treated indefinitely. Unprovoked VTE, which occurs in the absence of any identifiable risk factor, has a high risk of recurrence and may require indefinite anticoagulation, depending on the patient's characteristics and preferences.[3][7][8] The risk of recurrence of thrombosis also plays a role in treatment duration. In general, patients who experience a major reversible risk factor such as major trauma or surgery, have a lower incidence of recurrence and require less treatment time.[9] Those whos thrombosis is brought on by a minor reversible risk factor have a higher change of recurrent thrombus and require longer treatment time. These events include long flights, estrogen therapy, pregnancy and peripartum, and minor leg traumas. [9] It should also be noted that all patients with a first time VTE, regardless of what brought on the initial thrombosis, have a 50% chance of recurrence in the first 8-10 years after anticoagulation is discontinued. [9]
Factors that favor indefinite anticoagulation include male sex, presentation as PE (especially with concomitant DVT), positive d-dimer test after stopping anticoagulation, presence of antiphospholipid antibodies, low bleeding risk, and patient preference.[2] The type of anticoagulant used for indefinite therapy is of secondary importance, but low-dose DOACs may offer a convenient and safer option for some patients.[3][5][7][8] For cancer-associated VTE, full-dose DOACs are now preferred over LMWHs, unless there are gastrointestinal lesions that increase the risk of bleeding.[3][5][7][8]
Graduated compression stockings are elastic garments that apply a gradient of pressure to the lower limbs, reducing venous stasis and improving blood flow, still these stockings are not routinely indicated after DVT, but may be helpful if there is persistent leg swelling or symptomatic improvement with a trial of stockings.[2][10] Medications, such as pentoxifylline, have a limited role in the treatment of PTS. After PE, patients should be monitored for signs and symptoms of CTEPH, which is a rare but serious complication of VTE.[3][5][7][8] Ventilation-perfusion scanning and echocardiography are the initial diagnostic tests for CTEPH, and patients with confirmed or suspected CTEPH should be evaluated for potential treatments, such as pulmonary thromboendarterectomy, balloon pulmonary angioplasty, or vasodilator therapies.[2]
Risk Factors
[edit]There are several factors that increase the risk of developing a VTE.
High Risk: bone fracture (especially of the hip or leg), recent hip or knee replacement, recent major general surgery, spinal cord injuries, and major trauma.[11]
Moderate Risk Factors: arthroscopic knee surgery, central venous lines, chemotherapy, congestive heart failure, respiratory failure, hormone replacement therapy, cancer, use of oral contraceptives, pregnancy and the postpartum period, history of a previous VTE, and conditions such as thrombophilia.[11]
Low Risk Factors: prolonged immobility (long car/plane ride, bed rest duration >3 days), increased age, laparoscopic surgeries, obesity, and varicose veins.[11]
Prophylaxis
[edit]Being an inpatient is also a risk factor for developing a VTE. It is suggested that most hospitalized patients should be given some type of thromboprophylaxis. Some options include unfractionated heparin (UFH), low-molecular weight heparin (LMWH) such as enoxaparin, and Vitamin K antagonists. [11]
Arterial thromboembolism
[edit][edit] Main article: Arterial thromboembolism
Arterial thromboembolism (ATE) is a less common, but more severe form of thromboembolism, which can affect various organs, such as the brain, heart, kidneys, limbs, and mesentery.
ATE can cause life-threatening conditions, such as stroke, myocardial infarction, acute kidney injury, limb ischemia, and mesenteric ischemia. ATE is usually caused by atherosclerosis, which leads to plaque rupture and thrombus formation, or by cardioembolism, which results from the embolization of a cardiac thrombus, such as in atrial fibrillation, valvular disease, or myocardial dysfunction.
Etiology
[edit]There are several types of arterial thromboembolism that stem from different areas of the body. As briefly mentioned above, ATEs can cause strokes and harm to bodily organs. Some factors that play a role in risk of ATE formation are mesenteric artery disease, renal artery disease, aortoiliac occlusive disease, and lower extremity arterial occlusive disease.[12] These conditions are generally due to atherosclerosis. There are also several nonatherosclerotic conditions that can lead to ATE. Included in these conditions are giant cell arteritis, Takayasu's arteritis, Ehlers-Danlos syndrome, Marfan's syndrome, pseudoxanthoma elasticum, and Kawasaki's disease, and radiation induced arteritis.[12]The chronic inflammation of arteries caused by these conditions can lead to thickening of the vessel wall, fibrosis, stenosis, and ultimately thrombus formation.[12]
Treatment
[edit]The management of ATE depends on the location and severity of the ischemia and the underlying etiology. The main goals of ATE management are to restore blood flow, prevent further thrombosis, and treat the underlying cause. The treatment options for ATE include antithrombotic therapy, revascularization procedures, and risk factor modification. Antithrombotic therapy consists of antiplatelet agents, such as aspirin or clopidogrel, or anticoagulants, such as heparin or DOACs, depending on the indication and contraindications. Revascularization procedures include thrombolysis, thrombectomy, angioplasty, stenting, or bypass surgery and are indicated for patients with severe or limb-threatening ischemia or failed medical therapy.
Risk Factors and Prophylactic Lifestyle Changes
[edit]Risk factor modification involves lifestyle changes, such as smoking cessation, exercise, and diet, and pharmacological interventions, such as statins, antihypertensives, and glucose-lowering agents, to reduce the risk of recurrent ATE and improve the prognosis. The duration of antithrombotic therapy for ATE is variable, depending on the type and location of the thrombus, the presence of a prosthetic device, and the bleeding risk. In general, patients with ATE receive lifelong antiplatelet therapy unless there is a specific indication or contraindication for anticoagulation.[1][13]
References
[edit]- ^ a b c Tan, Boun Kim; Mainbourg, Sabine; Friggeri, Arnaud; Bertoletti, Laurent; Douplat, Marion; Dargaud, Yesim; Grange, Claire; Lobbes, Hervé; Provencher, Steeve; Lega, Jean-Christophe (2021-10). "Arterial and venous thromboembolism in COVID-19: a study-level meta-analysis". Thorax. 76 (10): 970–979. doi:10.1136/thoraxjnl-2020-215383. ISSN 0040-6376.
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(help) - ^ a b c d e f g h Donnellan, Eoin; Khorana, Alok A. (2017-02-01). "Cancer and Venous Thromboembolic Disease: A Review". The Oncologist. 22 (2): 199–207. doi:10.1634/theoncologist.2016-0214. ISSN 1083-7159. PMC 5330704. PMID 28174293.
- ^ a b c d e f g h i j Bartholomew, John R. (2017-12). "Update on the management of venous thromboembolism". Cleveland Clinic Journal of Medicine. 84 (12 Suppl 3): 39–46. doi:10.3949/ccjm.84.s3.04. ISSN 1939-2869. PMID 29257737.
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(help) - ^ a b c d e Blitzer, Rachel R.; Eisenstein, Samuel (2021-10). "Venous Thromboembolism and Pulmonary Embolism: Strategies for Prevention and Management". The Surgical Clinics of North America. 101 (5): 925–938. doi:10.1016/j.suc.2021.06.015. ISSN 1558-3171. PMID 34537152.
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(help) - ^ a b c d Phillippe, Haley M. (2017-12). "Overview of venous thromboembolism". The American Journal of Managed Care. 23 (20 Suppl): S376 – S382. ISSN 1936-2692. PMID 29297660.
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(help) - ^ "Venous Thromboembolism - Causes and Risk Factors | NHLBI, NIH". www.nhlbi.nih.gov. 2022-09-19. Retrieved 2025-05-07.
- ^ a b c d Kearon, Clive; Kahn, Susan R. (2020-01-30). "Long-term treatment of venous thromboembolism". Blood. 135 (5): 317–325. doi:10.1182/blood.2019002364. ISSN 1528-0020. PMID 31917402.
- ^ a b c d Yamashita, Yugo; Morimoto, Takeshi; Kimura, Takeshi (2022-01). "Venous thromboembolism: Recent advancement and future perspective". Journal of Cardiology. 79 (1): 79–89. doi:10.1016/j.jjcc.2021.08.026. ISSN 1876-4738. PMID 34518074.
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(help) - ^ a b c Prandoni, Paolo; Piovella, Chiara; Spiezia, Luca; Dalla Valle, Fabio; Pesavento, Raffaele (2011-07). "Optimal duration of anticoagulation in patients with venous thromboembolism". The Indian Journal of Medical Research. 134 (1): 15–21. ISSN 0971-5916. PMC 3171911. PMID 21808129.
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(help) - ^ Jeffery, P. C.; Nicolaides, A. N. (1990-04). "Graduated compression stockings in the prevention of postoperative deep vein thrombosis". The British Journal of Surgery. 77 (4): 380–383. doi:10.1002/bjs.1800770407. ISSN 0007-1323. PMID 2187559.
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(help) - ^ a b c d Merli, Geno J. (2005-01-01). "Venous thromboembolism prophylaxis guidelines: Use by primary care physicians". Clinical Cornerstone. Prevention of Thromboembolic Events. 7 (4): 32–38. doi:10.1016/S1098-3597(05)80101-2. ISSN 1098-3597.
- ^ a b c Schein, Moshe (2010-02-17). "Schwartz's Principles of Surgery, F. Charles Brunicardi, Dana K. Andersen, Timothy R. Billiar, David L. Dunn, John G. Hunter, Jeffrey B. Matthews, Raphael E. Pollock (Eds)". World Journal of Surgery. 34 (4): 871–873. doi:10.1007/s00268-010-0447-y. ISSN 0364-2313.
- ^ Stadnicki, Antoni; Stadnicka, Izabela (2021-10-28). "Venous and arterial thromboembolism in patients with inflammatory bowel diseases". World Journal of Gastroenterology. 27 (40): 6757–6774. doi:10.3748/wjg.v27.i40.6757. ISSN 2219-2840. PMC 8567469. PMID 34790006.
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