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Venous thrombosis

From Wikipedia, the free encyclopedia
Venous thrombosis
A deep vein thrombosis in the right leg. There is striking redness and swelling.
SpecialtyHematology, pulmonology, cardiology
Frequency1-2 per 1,000 per year[1]

Venous thrombosis is the blockage of a vein caused by a thrombus (blood clot). A common form of venous thrombosis is deep vein thrombosis (DVT), when a blood clot forms in the deep veins. If a thrombus breaks off (embolizes) and flows to the lungs to lodge there, it becomes a pulmonary embolism (PE), a blood clot in the lungs. The conditions of DVT only, DVT with PE, and PE only, are all captured by the term venous thromboembolism (VTE).[2]

The initial treatment for VTE is typically either low-molecular-weight heparin (LMWH) or unfractionated heparin, or increasingly with direct acting oral anticoagulants (DOAC). Those initially treated with heparins can be switched to other anticoagulants (warfarin, DOACs), although pregnant women and some people with cancer receive ongoing heparin treatment. Superficial venous thrombosis or phlebitis affects the superficial veins of the upper or lower extremity and only require anticoagulation in specific situations, and may be treated with anti-inflammatory pain relief only.

There are other less common forms of venous thrombosis, some of which can also lead to pulmonary embolism. Venous thromboembolism and superficial vein thrombosis account for about 90% of venous thrombosis. Other rarer forms include retinal vein thrombosis, mesenteric vein thrombosis (affecting veins draining blood from the gastrointestinal organs), cerebral venous sinus thrombosis, renal vein thrombosis, and ovarian vein thrombosis.[3]

Classification

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Common forms

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Superficial venous thromboses cause discomfort but generally not serious consequences, as do the deep vein thromboses (DVTs) that form in the deep veins of the legs or in the pelvic veins. Nevertheless, they can progress to the deep veins through the perforator veins or, they can be responsible for a lung embolism mainly if the head of the clot is poorly attached to the vein wall and is situated near the sapheno-femoral junction.[citation needed]

When a blood clot breaks loose and travels in the blood, this is called a thromboembolism. The abbreviation DVT/PE refers to a VTE where a deep vein thrombosis (DVT) has moved to the lungs (PE or pulmonary embolism).[4]

Since the veins return blood to the heart, if a piece of a blood clot formed in a vein breaks off it can be transported to the right side of the heart, and from there into the lungs. A piece of thrombus that is transported in this way is an embolus: the process of forming a thrombus that becomes embolic is called a thromboembolism. An embolism that lodges in the lungs is a pulmonary embolism (PE). A pulmonary embolism is a very serious condition that can be fatal depending on the dimensions of the embolus.[citation needed]

Rare forms

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While venous thrombosis of the legs is the most common form, venous thrombosis may occur in other veins. These may have particular specific risk factors:[5]

Parodoxical embolism

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Systemic embolism of venous origin can occur in patients with an atrial or ventricular septal defect, or an arteriovenous connection in the lung, through which an embolus may pass into the arterial system. Such an event is termed a paradoxical embolism. When this affects the blood vessels of the brain it can cause stroke.[6]

Causes

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Venous thrombi are caused mainly by a combination of venous stasis and hypercoagulability—but to a lesser extent endothelial damage and activation.[7] The three factors of stasis, hypercoagulability, and alterations in the blood vessel wall represent Virchow's triad, and changes to the vessel wall are the least understood.[8] Various risk factors increase the likelihood of any one individual developing a thrombosis:

Risk factors

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Acquired

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Inherited

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Mixed

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The overall absolute risk of venous thrombosis per 100,000 woman years in current use of combined oral contraceptives is approximately 60, compared to 30 in non-users.[23] The risk of thromboembolism varies with different types of birth control pills; Compared with combined oral contraceptives containing levonorgestrel (LNG), and with the same dose of estrogen and duration of use, the rate ratio of deep vein thrombosis for combined oral contraceptives with norethisterone is 0.98, with norgestimate 1.19, with desogestrel (DSG) 1.82, with gestodene 1.86, with drospirenone (DRSP) 1.64, and with cyproterone acetate 1.88.[23] Venous thromboembolism occurs in 100–200 per 100,000 pregnant women every year.[23]

Regarding family history, age has substantial effect modification. For people with two or more affected siblings, the highest incidence rate is found among those ≥70 years of age (390 per 100,000 in men and 370 per 100,000 in women), whereas the highest incidence ratios compared to those without affected siblings occurred at much younger ages (ratio of 4.3 among men 20 to 29 years of age and 5.5 among women 10 to 19 years of age).[24]

Risk of venous thromboembolism (VTE) with hormone therapy and birth control (QResearch/CPRD)
Type Route Medications Odds ratio (95% CITooltip confidence interval)
Menopausal hormone therapy Oral Estradiol alone
    ≤1 mg/day
    >1 mg/day		 1.27 (1.16–1.39)*
1.22 (1.09–1.37)*
1.35 (1.18–1.55)*
Conjugated estrogens alone
    ≤0.625 mg/day
    >0.625 mg/day		 1.49 (1.39–1.60)*
1.40 (1.28–1.53)*
1.71 (1.51–1.93)*
Estradiol/medroxyprogesterone acetate 1.44 (1.09–1.89)*
Estradiol/dydrogesterone
    ≤1 mg/day E2
    >1 mg/day E2		 1.18 (0.98–1.42)
1.12 (0.90–1.40)
1.34 (0.94–1.90)
Estradiol/norethisterone
    ≤1 mg/day E2
    >1 mg/day E2		 1.68 (1.57–1.80)*
1.38 (1.23–1.56)*
1.84 (1.69–2.00)*
Estradiol/norgestrel or estradiol/drospirenone 1.42 (1.00–2.03)
Conjugated estrogens/medroxyprogesterone acetate 2.10 (1.92–2.31)*
Conjugated estrogens/norgestrel
    ≤0.625 mg/day CEEs
    >0.625 mg/day CEEs		 1.73 (1.57–1.91)*
1.53 (1.36–1.72)*
2.38 (1.99–2.85)*
Tibolone alone 1.02 (0.90–1.15)
Raloxifene alone 1.49 (1.24–1.79)*
Transdermal Estradiol alone
   ≤50 μg/day
   >50 μg/day		 0.96 (0.88–1.04)
0.94 (0.85–1.03)
1.05 (0.88–1.24)
Estradiol/progestogen 0.88 (0.73–1.01)
Vaginal Estradiol alone 0.84 (0.73–0.97)
Conjugated estrogens alone 1.04 (0.76–1.43)
Combined birth control Oral Ethinylestradiol/norethisterone 2.56 (2.15–3.06)*
Ethinylestradiol/levonorgestrel 2.38 (2.18–2.59)*
Ethinylestradiol/norgestimate 2.53 (2.17–2.96)*
Ethinylestradiol/desogestrel 4.28 (3.66–5.01)*
Ethinylestradiol/gestodene 3.64 (3.00–4.43)*
Ethinylestradiol/drospirenone 4.12 (3.43–4.96)*
Ethinylestradiol/cyproterone acetate 4.27 (3.57–5.11)*
Notes: (1) Nested case–control studies (2015, 2019) based on data from the QResearch and Clinical Practice Research Datalink (CPRD) databases. (2) Bioidentical progesterone was not included, but is known to be associated with no additional risk relative to estrogen alone. Footnotes: * = Statistically significant (p < 0.01). Sources: See template.
Absolute and relative incidence of venous thromboembolism (VTE) during pregnancy and the postpartum period
Absolute incidence of first VTE per 10,000 person–years during pregnancy and the postpartum period
Swedish data A Swedish data B English data Danish data
Time period N Rate (95% CI) N Rate (95% CI) N Rate (95% CI) N Rate (95% CI)
Outside pregnancy 1105 4.2 (4.0–4.4) 1015 3.8 (?) 1480 3.2 (3.0–3.3) 2895 3.6 (3.4–3.7)
Antepartum 995 20.5 (19.2–21.8) 690 14.2 (13.2–15.3) 156 9.9 (8.5–11.6) 491 10.7 (9.7–11.6)
  Trimester 1 207 13.6 (11.8–15.5) 172 11.3 (9.7–13.1) 23 4.6 (3.1–7.0) 61 4.1 (3.2–5.2)
  Trimester 2 275 17.4 (15.4–19.6) 178 11.2 (9.7–13.0) 30 5.8 (4.1–8.3) 75 5.7 (4.6–7.2)
  Trimester 3 513 29.2 (26.8–31.9) 340 19.4 (17.4–21.6) 103 18.2 (15.0–22.1) 355 19.7 (17.7–21.9)
Around delivery 115 154.6 (128.8–185.6) 79 106.1 (85.1–132.3) 34 142.8 (102.0–199.8)
–
Postpartum 649 42.3 (39.2–45.7) 509 33.1 (30.4–36.1) 135 27.4 (23.1–32.4) 218 17.5 (15.3–20.0)
  Early postpartum 584 75.4 (69.6–81.8) 460 59.3 (54.1–65.0) 177 46.8 (39.1–56.1) 199 30.4 (26.4–35.0)
  Late postpartum 65 8.5 (7.0–10.9) 49 6.4 (4.9–8.5) 18 7.3 (4.6–11.6) 319 3.2 (1.9–5.0)
Incidence rate ratios (IRRs) of first VTE during pregnancy and the postpartum period
Swedish data A Swedish data B English data Danish data
Time period IRR* (95% CI) IRR* (95% CI) IRR (95% CI)† IRR (95% CI)†
Outside pregnancy
Reference (i.e., 1.00)
Antepartum 5.08 (4.66–5.54) 3.80 (3.44–4.19) 3.10 (2.63–3.66) 2.95 (2.68–3.25)
  Trimester 1 3.42 (2.95–3.98) 3.04 (2.58–3.56) 1.46 (0.96–2.20) 1.12 (0.86–1.45)
  Trimester 2 4.31 (3.78–4.93) 3.01 (2.56–3.53) 1.82 (1.27–2.62) 1.58 (1.24–1.99)
  Trimester 3 7.14 (6.43–7.94) 5.12 (4.53–5.80) 5.69 (4.66–6.95) 5.48 (4.89–6.12)
Around delivery 37.5 (30.9–44.45) 27.97 (22.24–35.17) 44.5 (31.68–62.54)
–
Postpartum 10.21 (9.27–11.25) 8.72 (7.83–9.70) 8.54 (7.16–10.19) 4.85 (4.21–5.57)
  Early postpartum 19.27 (16.53–20.21) 15.62 (14.00–17.45) 14.61 (12.10–17.67) 8.44 (7.27–9.75)
  Late postpartum 2.06 (1.60–2.64) 1.69 (1.26–2.25) 2.29 (1.44–3.65) 0.89 (0.53–1.39)
Notes: Swedish data A = Using any code for VTE regardless of confirmation. Swedish data B = Using only algorithm-confirmed VTE. Early postpartum = First 6 weeks after delivery. Late postpartum = More than 6 weeks after delivery. * = Adjusted for age and calendar year. † = Unadjusted ratio calculated based on the data provided. Source: [25]

Pathophysiology

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In contrast to the understanding for how arterial thromboses occur, as with heart attacks, venous thrombosis formation is not well understood.[26] With arterial thrombosis, blood vessel wall damage is required for thrombosis formation, as it initiates coagulation,[26] but the majority of venous thrombi form without any injured epithelium.[7]

Red blood cells and fibrin are the main components of venous thrombi,[7] and the thrombi appear to attach to the blood vessel wall endothelium, normally a non-thrombogenic surface, with fibrin.[26] Platelets in venous thrombi attach to downstream fibrin, while in arterial thrombi, they compose the core.[26] As a whole, platelets constitute less of venous thrombi when compared to arterial ones.[7] The process is thought to be initiated by tissue factor-affected thrombin production, which leads to fibrin deposition.[8]

The valves of veins are a recognized site of VT initiation. Due to the blood flow pattern, the base of the valve sinus is particularly deprived of oxygen (hypoxic). Stasis exacerbates hypoxia, and this state is linked to the activation of white blood cells (leukocytes) and the endothelium. Specifically, the two pathways of hypoxia-inducible factor-1 (HIF-1) and early growth response 1 (EGR-1) are activated by hypoxia, and they contribute to monocyte and endothelial activation. Hypoxia also causes reactive oxygen species (ROS) production that can activate HIF-1, EGR-1, and nuclear factor-κB (NF-κB), which regulates HIF-1 transcription.[8]

HIF-1 and EGR-1 pathways lead to monocyte association with endothelial proteins, such as P-selectin, prompting monocytes to release tissue factor-filled microvesicles, which presumably initiate fibrin deposition (via thrombin) after binding the endothelial surface.[8]

Diagnosis

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Prevention

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Main article: Thrombosis prophylaxis

Numerous medications have been shown to reduce the risk of a person having a VTE, however careful decision making is required in order to decide if a person's risk of having a VTE outweighs the risks associated with most thromboprophylaxis treatment approaches (medications to prevent venous thrombosis). It is recommended that people should be assessed at their hospital discharge for persistent high-risk of venous thrombosis and that people who adopt a heart-healthy lifestyle might lower their risk of venous thrombosis.[27] Clinical policy from the American College of Physicians states a lack of support for any performance measures that incentivize physicians to apply universal prophylaxis without regard to the risks.[28]

Surgery

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Evidence supports the use of heparin in people following surgery who have a high risk of thrombosis to reduce the risk of DVTs; however, the effect on PEs or overall mortality is not known.[29] In hospitalized non-surgical patients, mortality does not appear to change.[30][31][32] It does not appear, however, to decrease the rate of symptomatic DVTs.[30] Using both heparin and compression stockings appears better than either one alone in reducing the rate of DVT.[33]

Non-surgical medical conditions

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In hospitalized people who have had a stroke and not had surgery, mechanical measures (compression stockings) resulted in skin damage and no clinical improvement.[30] Data on the effectiveness of compression stockings among hospitalized non-surgical patients without stroke is scarce.[30]

The American College of Physicians (ACP) gave three strong recommendations with moderate quality evidence on VTE prevention in non-surgical patients:

  • that hospitalized patients be assessed for their risk of thromboembolism and bleeding before prophylaxis (prevention);
  • that heparin or a related drug is used if potential benefits are thought to outweigh potential harms;
  • and that graduated compression stockings not be used.[28]

In adults who have had their lower leg casted, braced, or otherwise immobilized for more than a week, LMWH may decrease the risk and severity of deep vein thrombosis, but does not have any effect on the incidence of pulmonary embolism.[34]

Prior VTE

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Following the completion of warfarin in those with prior VTE, the use of long-term aspirin has been shown to be beneficial.[35]

Cancer

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People who have cancer have a higher risk of VTE and may respond differently to anticoagulant preventative treatments and prevention measures.[36] The American Society of Hematology strongly suggests that people undergoing chemotherapy for cancer who are at low risk of a VTE avoid medications to prevent thrombosis (thromboprophylaxis).[37] For people undergoing chemotherapy for cancer that do not require a hospital stay (those undergoing ambulatory care), there is low certainty evidence to suggest that treatment with direct factor Xa inhibitors may help prevent symptomatic VTEs, however this treatment approach may also lead to an increase in the risk of a major bleed compared to a placebo medication.[38] There is stronger evidence to suggest that LMWH helps prevent symptomatic VTE, however this treatment approach also comes with a higher risk of a major bleed compared to a placebo medication or no treatments to prevent VTE.[38]

For people who are having surgery for cancer, it is recommended that they receive anticoagulation therapy (preferably LMWH) in order to prevent a VTE.[39] LMWH is recommended for at least 7–10 days following cancer surgery, and for one month following surgery for people who have a high risk of VTEs.[40][39]

Specifically for patients with various types of lymphoma, there is a risk assessment model, ThroLy, to help providers determine how likely a thromboembolic event is to occur.[41]

Treatment

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American evidence-based clinical guidelines were published in 2016 for the treatment of VTE.[42] In the UK, guidelines by the National Institute for Health and Care Excellence (NICE) were published in 2012, updated in 2020.[43] These guidelines do not cover rare forms of thrombosis, for which an individualized approach is often needed.[5] Central and branch retinal vein occlusion does not benefit from anticoagulation in the way that other venous thromboses do.[5]

Anticoagulation

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If diagnostic testing cannot be performed swiftly, many are commenced on empirical treatment.[43] Traditionally this was heparin, but several of the DOACs are licensed for treatment without initial heparin use.[42]

If heparin is used for initial treatment of VTE, fixed doses with low-molecular-weight heparin (LMWH) may be more effective than adjusted doses of unfractionated heparin (UFH) in reducing blood clots.[44] No differences in mortality, prevention of major bleeding, or preventing VTEs from recurring were observed between LMWH and UFH.[45] No differences have been detected in the route of administration of UFH (subcutaneous or intravenous).[44] LMWH is usually administered by a subcutaneous injection, and a person's blood clotting factors do not have to be monitored as closely as with UFH.[44]

Once the diagnosis is confirmed, a decision needs to be made about the nature of the ongoing treatment and its duration. USA recommendations for those without cancer include anticoagulation (medication that prevents further blood clots from forming) with the DOACs dabigatran, rivaroxaban, apixaban, or edoxaban rather than warfarin or low molecular weight heparin (LMWH).[42]

For those with cancer, LMWH is recommended,[42] although DOACs appear safe in the majority of situations.[43] For long-term treatment in people with cancer, LMWH is probably more effective at reducing VTEs when compared to vitamin K antagonists.[36] People with cancer have a higher risk of experiencing reoccurring VTE episodes ("recurrent VTE"), even while taking preventative anticoagulation medication. These people should be given therapeutic doses of LMWH medication, either by switching from another anticoagulant or by taking a higher dose of LMWH.[46]

In pregnancy, warfarin and DOACs are not considered suitable and LMWH is recommended.[42]

For those with a small pulmonary embolism and few risk factors, no anticoagulation is needed.[42] Anticoagulation is, however, recommended in those who do have risk factors.[42]

Thrombolysis

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Thrombolysis is the administration of medication (a recombinant enzyme) that activates plasmin, the body's main enzyme that breaks down blood clots. This carries a risk of bleeding and is therefore reserved for those who have a form of thrombosis that may cause major complications. In pulmonary embolism, this applies in situations where heart function is compromised due to lack of blood flow through the lungs ("massive" or "high risk" pulmonary embolism), leading to low blood pressure.[42] Deep vein thrombosis may require thrombolysis if there is a significant risk of post-thrombotic syndrome.[42] Thrombolysis may be administered by intravenous catheter directly into the clot ("catheter-directed thrombolysis"); this requires a lower dose of the medication and may carry a lower bleeding risk but evidence for its benefit is limited.[42]

Inferior vena cava filters

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Inferior vena cava filters (IVCFs) are not recommended in those who are on anticoagulants.[42] IVCFs may be used in clinical situations where a person has a high risk of experiencing a pulmonary embolism, but cannot be on anticoagulants due to a high risk of bleeding, or they have active bleeding.[46][47] Retrievable IVCFs are recommended if IVCFs must be used, and a plan should be created to remove the filter when it is no longer needed.[46]

Superficial venous thrombosis

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While topical treatments for superficial venous thrombosis are widely used, the evidence is strongest for the heparin-like drug fondaparinux (a factor Xa inhibitor), which reduces extension and recurrence of superficial venous thrombosis as well as progression to symptomatic embolism.[48]

Prognosis

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After an episode of unprovoked VTE, the risk of further episodes after completing treatment remains elevated, although this risk diminishes over time. Over ten years, 41% of men and 29% of women can expect to experience a further episode. For each episode, the risk of death is 4%.[49]

See also

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References

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  1. ^ Ortel, TL; Neumann, I; Ageno, W; et al. (13 October 2020). "American Society of Hematology 2020 guidelines for management of venous thromboembolism: treatment of deep vein thrombosis and pulmonary embolism". Blood Advances. 4 (19): 4693–4738. doi:10.1182/bloodadvances.2020001830. PMC 7556153. PMID 33007077.
  2. ^ Heit JA, Spencer FA, White RH (January 2016). "The epidemiology of venous thromboembolism". Journal of Thrombosis and Thrombolysis. 41 (1): 3–14. doi:10.1007/s11239-015-1311-6. PMC 4715842. PMID 26780736.
  3. ^ a b Abbattista M, Capecchi M, Martinelli I (January 2020). "Treatment of unusual thrombotic manifestations". Blood. 135 (5): 326–334. doi:10.1182/blood.2019000918. PMID 31917405.
  4. ^ National Clinical Guideline Centre – Acute and Chronic Conditions (UK) (2010). "Venous Thromboembolism: Reducing the Risk of Venous Thromboembolism (Deep Vein Thrombosis and Pulmonary Embolism) in Patients Admitted to Hospital". PMID 23346611. {{cite journal}}: Cite journal requires |journal= (help)
  5. ^ a b c Shatzel, Joseph J.; O'Donnell, Matthew; Olson, Sven R.; Kearney, Matthew R.; Daughety, Molly M.; Hum, Justine; Nguyen, Khanh P.; DeLoughery, Thomas G. (January 2019). "Venous thrombosis in unusual sites: A practical review for the hematologist". European Journal of Haematology. 102 (1): 53–62. doi:10.1111/ejh.13177. ISSN 0902-4441. PMID 30267448.
  6. ^ Windecker, Stephan; Stortecky, Stefan; Meier, Bernhard (July 2014). "Paradoxical Embolism". Journal of the American College of Cardiology. 64 (4): 403–415. doi:10.1016/j.jacc.2014.04.063. PMID 25060377.
  7. ^ a b c d e f g h i j k l m n o p Martinelli I, Bucciarelli P, Mannucci PM (2010). "Thrombotic risk factors: basic pathophysiology". Crit Care Med. 38 (suppl 2): S3–9. doi:10.1097/CCM.0b013e3181c9cbd9. PMID 20083911. S2CID 34486553.
  8. ^ a b c d e f g Bovill EG, van der Vliet A (2011). "Venous valvular stasis-associated hypoxia and thrombosis: what is the link?". Annu Rev Physiol. 73: 527–45. doi:10.1146/annurev-physiol-012110-142305. PMID 21034220.
  9. ^ a b c d e f g h i Rosendaal FR, Reitsma PH (2009). "Genetics of venous thrombosis". J. Thromb. Haemost. 7 (suppl 1): 301–4. doi:10.1111/j.1538-7836.2009.03394.x. PMID 19630821. S2CID 27104496.
  10. ^ Khan NR, Patel PG, Sharpe JP, Lee SL, Sorenson J (2018). "Chemical venous thromboembolism prophylaxis in neurosurgical patients: an updated systematic review and meta-analysis". Journal of Neurosurgery. 129 (4): 906–915. doi:10.3171/2017.2.JNS162040. PMID 29192859. S2CID 37464528. Patients requiring cranial and spinal surgery present a unique situation of elevated risk for VTE but also high risk for disastrous outcomes should bleeding complications occur in eloquent areas of the brain or spinal cord.Open access icon
  11. ^ Stein PD, Beemath A, Meyers FA, et al. (2006). "Incidence of venous thromboembolism in patients hospitalized with cancer". Am J Med. 119 (1): 60–8. doi:10.1016/j.amjmed.2005.06.058. PMID 16431186.
  12. ^ Jackson E, Curtis KM, Gaffield ME (2011). "Risk of venous thromboembolism during the postpartum period: a systematic review". Obstet Gynecol. 117 (3): 691–703. doi:10.1097/AOG.0b013e31820ce2db. PMID 21343773. S2CID 12561.
  13. ^ Varga EA, Kujovich JL (2012). "Management of inherited thrombophilia: guide for genetics professionals". Clin Genet. 81 (1): 7–17. doi:10.1111/j.1399-0004.2011.01746.x. PMID 21707594. S2CID 9305488.
  14. ^ Turpie AGG (March 2008). "Deep Venous Thrombosis". The Merck's Manuals Online Medical Library. Merck. Archived from the original on 2020-03-13. Retrieved 2012-08-02.
  15. ^ Beyer-Westendorf J, Bauersachs R, Hach-Wunderle V, Zotz RB, Rott H. Sex hormones and venous thromboembolism - from contraception to hormone replacement therapy. Vasa. 2018 Jul 16:1-10.2018/07/17
  16. ^ Reitsma PH, Versteeg HH, Middeldorp S (2012). "Mechanistic view of risk factors for venous thromboembolism". Arterioscler Thromb Vasc Biol. 32 (3): 563–8. doi:10.1161/ATVBAHA.111.242818. PMID 22345594. S2CID 2624599.
  17. ^ Zöller B, Li X, Sundquist J, et al. (2012). "Risk of pulmonary embolism in patients with autoimmune disorders: a nationwide follow-up study from Sweden". Lancet. 379 (9812): 244–9. doi:10.1016/S0140-6736(11)61306-8. PMID 22119579. S2CID 11612703.
  18. ^ a b c d e f Lijfering WM, Rosendaal FR, Cannegieter SC (2010). "Risk factors for venous thrombosis – current understanding from an epidemiological point of view". Br J Haematol. 149 (6): 824–33. doi:10.1111/j.1365-2141.2010.08206.x. PMID 20456358. S2CID 41684138.
  19. ^ Mandalà, M; Falanga, A; Roila, F; ESMO Guidelines Working, Group. (September 2011). "Management of venous thromboembolism (VTE) in cancer patients: ESMO Clinical Practice Guidelines". Annals of Oncology. 22 (Suppl 6): vi85–92. doi:10.1093/annonc/mdr392. PMID 21908511.
  20. ^ Tang L, Wu YY, Lip GY, Yin P, Hu Y (January 2016). "Heart failure and risk of venous thromboembolism: a systematic review and meta-analysis". Lancet Haematol. 3 (1): e30–44. doi:10.1016/S2352-3026(15)00228-8. PMID 26765646.
  21. ^ Dentali F, Sironi AP, Ageno W, et al. (2012). "Non-O Blood Type Is the Commonest Genetic Risk Factor for VTE: Results from a Meta-Analysis of the Literature". Semin. Thromb. Hemost. 38 (5): 535–48. doi:10.1055/s-0032-1315758. PMID 22740183. S2CID 5203474.
  22. ^ Jenkins PV, Rawley O, Smith OP, et al. (2012). "Elevated factor VIII levels and risk of venous thrombosis". Br J Haematol. 157 (6): 653–63. doi:10.1111/j.1365-2141.2012.09134.x. PMID 22530883. S2CID 24467063.
  23. ^ a b c Eichinger, S.; Evers, J. L. H.; Glasier, A.; La Vecchia, C.; Martinelli, I.; Skouby, S.; Somigliana, E.; Baird, D. T.; Benagiano, G.; Crosignani, P. G.; Gianaroli, L.; Negri, E.; Volpe, A.; Glasier, A.; Crosignani, P. G. (2013). "Venous thromboembolism in women: A specific reproductive health risk". Human Reproduction Update. 19 (5): 471–482. doi:10.1093/humupd/dmt028. PMID 23825156.
  24. ^ Eikelboom, J. W.; Weitz, J. I. (2011). "Importance of family history as a risk factor for venous thromboembolism". Circulation. 124 (9): 996–7. doi:10.1161/CIRCULATIONAHA.111.048868. PMID 21875920.
  25. ^ Abdul Sultan A, West J, Stephansson O, Grainge MJ, Tata LJ, Fleming KM, Humes D, Ludvigsson JF (November 2015). "Defining venous thromboembolism and measuring its incidence using Swedish health registries: a nationwide pregnancy cohort study". BMJ Open. 5 (11): e008864. doi:10.1136/bmjopen-2015-008864. PMC 4654387. PMID 26560059.
  26. ^ a b c d López JA, Chen J (2009). "Pathophysiology of venous thrombosis". Thromb Res. 123 (Suppl 4): S30–4. doi:10.1016/S0049-3848(09)70140-9. PMID 19303501.
  27. ^ Goldhaber, Samuel Z. (2010). "Risk Factors for Venous Thromboembolism". Journal of the American College of Cardiology. 56 (1): 1–7. doi:10.1016/j.jacc.2010.01.057. PMID 20620709.
  28. ^ a b Qaseem A, Chou R, Humphrey LL, Starkey M, Shekelle P (November 2011). "Venous thromboembolism prophylaxis in hospitalized patients: a clinical practice guideline from the American College of Physicians". Ann. Intern. Med. 155 (9): 625–32. CiteSeerX 10.1.1.689.591. doi:10.7326/0003-4819-155-9-201111010-00011. PMID 22041951. S2CID 7129943.
  29. ^ Roderick, P; Ferris, G; Wilson, K; Halls, H; Jackson, D; Collins, R; Baigent, C (December 2005). "Towards evidence-based guidelines for the prevention of venous thromboembolism: systematic reviews of mechanical methods, oral anticoagulation, dextran and regional anaesthesia as thromboprophylaxis". Health Technology Assessment. 9 (49): iii–iv, ix–x, 1–78. doi:10.3310/hta9490. PMID 16336844.
  30. ^ a b c d Lederle, FA; Zylla, D; Macdonald, R; Wilt, TJ (2011-11-01). "Venous thromboembolism prophylaxis in hospitalized medical patients and those with stroke: a background review for an american college of physicians clinical practice guideline". Annals of Internal Medicine. 155 (9): 602–15. doi:10.7326/0003-4819-155-9-201111010-00008. PMID 22041949. S2CID 207536371.
  31. ^ Alikhan, R; Bedenis, R; Cohen, AT (7 May 2014). "Heparin for the prevention of venous thromboembolism in acutely ill medical patients (excluding stroke and myocardial infarction)". The Cochrane Database of Systematic Reviews. 2018 (5): CD003747. doi:10.1002/14651858.CD003747.pub4. PMC 6491079. PMID 24804622.
  32. ^ "[120] Routine VTE prophylaxis: Is there a net health benefit?". Therapeutics Initiative. 16 July 2019.
  33. ^ Zareba, P; Wu, C; Agzarian, J; Rodriguez, D; Kearon, C (Aug 2014). "Meta-analysis of randomized trials comparing combined compression and anticoagulation with either modality alone for prevention of venous thromboembolism after surgery". The British Journal of Surgery. 101 (9): 1053–62. doi:10.1002/bjs.9527. PMID 24916118. S2CID 37373926.
  34. ^ Zee, AA; van Lieshout, K; van der Heide, M; Janssen, L; Janzing, HM (Apr 25, 2017). "Low molecular weight heparin for prevention of venous thromboembolism in patients with lower-leg immobilization". The Cochrane Database of Systematic Reviews. 2017 (8): CD006681. doi:10.1002/14651858.CD006681.pub4. PMC 6483324. PMID 28780771.
  35. ^ Simes, J; Becattini, C; Agnelli, G; Eikelboom, JW; Kirby, AC; Mister, R; Prandoni, P; Brighton, TA; INSPIRE Study Investigators (International Collaboration of Aspirin Trials for Recurrent Venous, Thromboembolism) (23 September 2014). "Aspirin for the prevention of recurrent venous thromboembolism: the INSPIRE collaboration". Circulation. 130 (13): 1062–71. doi:10.1161/circulationaha.114.008828. PMID 25156992.
  36. ^ a b Kahale, Lara A.; Hakoum, Maram B.; Tsolakian, Ibrahim G.; Matar, Charbel F.; Terrenato, Irene; Sperati, Francesca; Barba, Maddalena; Yosuico, Victor Ed; Schünemann, Holger (2018). "Anticoagulation for the long-term treatment of venous thromboembolism in people with cancer". The Cochrane Database of Systematic Reviews. 2022 (6): CD006650. doi:10.1002/14651858.CD006650.pub5. ISSN 1469-493X. PMC 6389342. PMID 29920657.
  37. ^ Lyman, Gary H.; Carrier, Marc; Ay, Cihan; Di Nisio, Marcello; Hicks, Lisa K.; Khorana, Alok A.; Leavitt, Andrew D.; Lee, Agnes Y. Y.; Macbeth, Fergus; Morgan, Rebecca L.; Noble, Simon (2021-02-23). "American Society of Hematology 2021 guidelines for management of venous thromboembolism: prevention and treatment in patients with cancer". Blood Advances. 5 (4): 927–974. doi:10.1182/bloodadvances.2020003442. ISSN 2473-9537. PMC 7903232. PMID 33570602.
  38. ^ a b Rutjes, Anne Ws; Porreca, Ettore; Candeloro, Matteo; Valeriani, Emanuele; Di Nisio, Marcello (2020-12-18). "Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy". The Cochrane Database of Systematic Reviews. 2020 (12): CD008500. doi:10.1002/14651858.CD008500.pub5. ISSN 1469-493X. PMC 8829903. PMID 33337539.
  39. ^ a b Mandalà, M.; Falanga, A.; Roila, F.; ESMO Guidelines Working Group (2011-09-01). "Management of venous thromboembolism (VTE) in cancer patients: ESMO Clinical Practice Guidelines". Annals of Oncology. 22 (Suppl 6): vi85–92. doi:10.1093/annonc/mdr392. ISSN 1569-8041. PMID 21908511.
  40. ^ Christensen, Thomas D.; Vad, Henrik; Pedersen, Søren; Hvas, Anne-Mette; Wotton, Robin; Naidu, Babu; Larsen, Torben B. (2014-02-01). "Venous thromboembolism in patients undergoing operations for lung cancer: a systematic review". The Annals of Thoracic Surgery. 97 (2): 394–400. doi:10.1016/j.athoracsur.2013.10.074. ISSN 1552-6259. PMID 24365217.
  41. ^ Antic, Darko; Milic, Natasa; Nikolovski, Srdjan; Todorovic, Milena; Bila, Jelena; Djurdjevic, Predrag; Andjelic, Bosko; Djurasinovic, Vladislava; Sretenovic, Aleksandra; Vukovic, Vojin; Jelicic, Jelena; Hayman, Suzanne; Mihaljevic, Biljana (July 2016). "Development and validation of multivariable predictive model for thromboembolic events in lymphoma patients". American Journal of Hematology. 91 (10): 1014–1019. doi:10.1002/ajh.24466. ISSN 0361-8609.
  42. ^ a b c d e f g h i j k Kearon, C; Akl, EA; Ornelas, J; Blaivas, A; Jimenez, D; Bounameaux, H; Huisman, M; King, CS; Morris, TA; Sood, N; Stevens, SM; Vintch, JR; Wells, P; Woller, SC; Moores, L (February 2016). "Antithrombotic Therapy for VTE Disease: CHEST Guideline and Expert Panel Report". Chest. 149 (2): 315–52. doi:10.1016/j.chest.2015.11.026. PMID 26867832.
  43. ^ a b c "Venous thromboembolic diseases: diagnosis, management and thrombophilia testing". www.nice.org.uk. National Institute for Health and Care Excellence. 2020. Retrieved 2020-08-31.
  44. ^ a b c Robertson, Lindsay; Jones, Lauren E. (2017-02-09). "Fixed dose subcutaneous low molecular weight heparins versus adjusted dose unfractionated heparin for the initial treatment of venous thromboembolism". The Cochrane Database of Systematic Reviews. 2017 (2): CD001100. doi:10.1002/14651858.CD001100.pub4. ISSN 1469-493X. PMC 6464611. PMID 28182249.
  45. ^ Robertson L, Strachan J (February 2017). "Subcutaneous unfractionated heparin for the initial treatment of venous thromboembolism". Cochrane Database Syst Rev. 2 (11): CD006771. doi:10.1002/14651858.CD006771.pub3. PMC 6464347. PMID 28195640.
  46. ^ a b c Khorana, Alok A.; Carrier, Marc; Garcia, David A.; Lee, Agnes Y. Y. (2016-01-01). "Guidance for the prevention and treatment of cancer-associated venous thromboembolism". Journal of Thrombosis and Thrombolysis. 41 (1): 81–91. doi:10.1007/s11239-015-1313-4. ISSN 1573-742X. PMC 4715852. PMID 26780740.
  47. ^ Rajasekhar, Anita (2015-04-01). "Inferior vena cava filters: current best practices". Journal of Thrombosis and Thrombolysis. 39 (3): 315–327. doi:10.1007/s11239-015-1187-5. ISSN 1573-742X. PMID 25680894. S2CID 5868257.
  48. ^ Di Nisio, Marcello; Wichers, Iris M; Middeldorp, Saskia (2018-02-25). Cochrane Vascular Group (ed.). "Treatment for superficial thrombophlebitis of the leg". Cochrane Database of Systematic Reviews. 2018 (2): CD004982. doi:10.1002/14651858.CD004982.pub6. PMC 6491080. PMID 29478266.
  49. ^ Khan, Faizan; Rahman, Alvi; Carrier, Marc; Kearon, Clive; Weitz, Jeffrey I; Schulman, Sam; Couturaud, Francis; Eichinger, Sabine; Kyrle, Paul A (2019-07-24). "Long term risk of symptomatic recurrent venous thromboembolism after discontinuation of anticoagulant treatment for first unprovoked venous thromboembolism event: systematic review and meta-analysis". BMJ. 366: l4363. doi:10.1136/bmj.l4363. PMC 6651066. PMID 31340984.
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