Jump to content

Anticoagulant

From Wikipedia, the free encyclopedia
(Redirected from NOACs)

Anticoagulant
Drug class
Coagulation cascade and major classes of anticoagulants
Class identifiers
ATC codeB01
External links
MeSHD00534-class
Legal status
In Wikidata

An anticoagulant, commonly known as a blood thinner, is a chemical substance that prevents or reduces the coagulation of blood, prolonging the clotting time.[1] Some occur naturally in blood-eating animals, such as leeches and mosquitoes, which help keep the bite area unclotted long enough for the animal to obtain blood.[2][3]

As a class of medications, anticoagulants are used in therapy for thrombotic disorders.[4] Oral anticoagulants (OACs) are taken by many people in pill or tablet form, and various intravenous anticoagulant dosage forms are used in hospitals.[5][6] Some anticoagulants are used in medical equipment, such as sample tubes, blood transfusion bags, heart–lung machines, and dialysis equipment.[7][8] One of the first anticoagulants, warfarin, was initially approved as a rodenticide.[9]

Anticoagulants are closely related to antiplatelet drugs and thrombolytic drugs by manipulating the various pathways of blood coagulation.[10] Specifically, antiplatelet drugs inhibit platelet aggregation (clumping together), whereas anticoagulants inhibit specific pathways of the coagulation cascade, which happens after the initial platelet aggregation but before the formation of fibrin and stable aggregated platelet products.[11][12]

Common anticoagulants include warfarin and heparin.[13]

Medical uses

[edit]

The use of anticoagulants is a decision based on the risks and benefits of anticoagulation.[14] The biggest risk of anticoagulation therapy is the increased risk of bleeding.[15] In otherwise healthy people, the increased risk of bleeding is minimal, but those who have had recent surgery, cerebral aneurysms, and other conditions may have too great a risk of bleeding.[16][17] Generally, the benefit of anticoagulation is preventing or reducing the progression of a thromboembolic disease.[18] Some indications for anticoagulant therapy that are known to have benefit from therapy include:

In these cases, anticoagulation therapy prevents the formation or growth of dangerous clots.[30]

The decision to begin therapeutic anticoagulation often involves the use of multiple bleeding risk predictable outcome tools as non-invasive pre-test stratifications due to the potential for bleeding while on blood thinning agents.[15] Among these tools are HAS-BLED,[31] ATRIA,[32] HEMORR2HAGES,[33] and CHA2DS2-VASc.[34] The risk of bleeding using the risk assessment tools above must then be weighed against thrombotic risk to formally determine the patient's overall benefit in starting anticoagulation therapy.[35]

There is no evidence to indicate that adding anticoagulant therapy to standard treatment has a benefit for people with cerebral small vessel disease but not dementia, and there is an increased risk of a person with this disease experiencing a bleed with this approach.[36]

Adverse effects

[edit]

The most serious and common adverse side effects associated with anticoagulants are increased risk of bleeding, both nonmajor and major bleeding events.[37] The bleeding risk depends on the class of anticoagulant agent used, the patient's age, and pre-existing health conditions. Warfarin has an estimated incidence of bleeding of 15-20% per year and a life-threatening bleeding rate of 1-3% per year.[38] Newer non-vitamin K antagonist oral anticoagulants appear to have fewer life-threatening bleeding events than warfarin.[39][40] Additionally, patients aged 80 years or more may be especially susceptible to bleeding complications, with a rate of 13 bleeds per 100 person-years.[41] Bleeding risk is especially important to consider in patients with renal impairment and NOAC therapy because all NOACs, to some extent, are excreted by the kidneys.[42] Thus, patients with renal impairment may be at higher risk of increased bleeding.[43]

In people with cancer, a systematic review has found warfarin had no effect on death rate or the risk of blood clots.[44] However, it did increase the risk of major bleeding in 107 more people per 1000 population and minor bleeding in 167 more people per 1000 population.[44] Apixaban had no effect on mortality, recurrence of blood clots in blood vessels, or major or minor bleeding. However, this finding comes only from one study.[44]

Nonhemorrhagic adverse events are less common than hemorrhagic adverse events but should still be monitored closely.[39] Nonhemorrhagic adverse events of warfarin include skin necrosis, limb gangrene, and purple toe syndrome.[45] Skin necrosis and limb gangrene are most commonly observed on the third to eighth day of therapy.[46][47] The exact pathogenesis of skin necrosis and limb gangrene is not completely understood but it is believed to be associated with warfarin's effect on inhibiting the production of protein C and protein S.[48][49] Purple toe syndrome typically develops three to eight weeks after initiation of warfarin therapy.[50][51] Other adverse effects of warfarin are associated with depletion of vitamin K, which can lead to inhibition of G1a proteins and growth arrest-specific gene 6, which can lead to increased risk of arterial calcification and heart valve, especially if too much Vitamin D is present.[52][53] Warfarin's interference with G1a proteins has also been linked to abnormalities in fetal bone development in mothers who were treated with warfarin during pregnancy.[54][55] Long-term warfarin and heparin usage have also been linked to osteoporosis.[56][45]

Another potentially severe complication associated with heparin use is called heparin-induced thrombocytopenia (HIT).[57] There are two distinct types: HIT 1) immune-mediated and 2) non-immune-mediated.[57] Immune-mediated HIT most commonly arises five to ten days after exposure to heparin.[58] Pathogenesis of immune-mediated HIT is believed to be caused by heparin-dependent immunoglobulin antibodies binding to platelet factor 4/heparin complexes on platelets, leading to widespread platelet activation.[59]

Interactions

[edit]

Foods and food supplements with blood-thinning effects include nattokinase, lumbrokinase, beer, bilberry, celery, cranberries, fish oil, garlic, ginger, ginkgo, ginseng, green tea, horse chestnut, licorice, niacin, onion, papaya, pomegranate, red clover, soybean, St. John's wort, turmeric, wheatgrass, and willow bark.[60][61][62] Many herbal supplements have blood-thinning properties, such as danshen and feverfew.[63] Multivitamins that do not interact with clotting are available for patients on anticoagulants.[64]

However, some foods and supplements encourage clotting.[65] These include alfalfa, avocado, cat's claw, coenzyme Q10, and dark leafy greens such as spinach.[66][67] Excessive intake of the food mentioned above should be avoided while taking anticoagulants, or if coagulability is being monitored, their intake should be kept approximately constant so that anticoagulant dosage can be maintained at a level high enough to counteract this effect without fluctuations in coagulability.[68][69]

Grapefruit interferes with some anticoagulant drugs, increasing the time it takes for them to be metabolized out of the body, and should be eaten with caution when on anticoagulant drugs.[70]

Anticoagulants are often used to treat acute deep-vein thrombosis.[71][72] People using anticoagulants to treat this condition should avoid using bed rest as a complementary treatment because there are clinical benefits to continuing to walk and remaining mobile while using anticoagulants in this way.[73] Bed rest while using anticoagulants can harm patients in circumstances in which it is not medically necessary.[73]

Types

[edit]

Several anticoagulants are available. Warfarin, other coumarins, and heparins have long been used.[74] Since the 2000s, several agents have been introduced that are collectively referred to as direct oral anticoagulants (DOACs), previously named novel oral anticoagulants (NOACs) or non-vitamin K antagonist oral anticoagulants.[75][76][77][78] These agents include direct thrombin inhibitor (dabigatran) and factor Xa inhibitor (rivaroxaban, apixaban, betrixaban and edoxaban), and they have been shown to be as good or possibly better than the coumarins with less serious side effects.[79] The newer anticoagulants (NOACs/DOACs) are more expensive than the traditional ones and should be used in caring for patients with kidney problems.[80]

Coumarins (vitamin K antagonists)

[edit]
Further information: Vitamin K antagonist

These oral anticoagulants are derived from coumarin found in many plants. A prominent member of this class, warfarin (Coumadin), was found to be the anticoagulant most prescribed in a large multispecialty practice.[81] The anticoagulant effect takes at least 48 to 72 hours to develop. Where an immediate effect is required, heparin is given concomitantly. These anticoagulants are used to treat patients with deep-vein thrombosis (DVT) and pulmonary embolism (PE) and to prevent emboli in patients with atrial fibrillation (AF), and mechanical prosthetic heart valves. Other examples are acenocoumarol, phenprocoumon, atromentin, and phenindione.[citation needed]

The coumarins brodifacoum and difenacoum are used as mammalicides (particularly as rodenticides) but are not used medically.[citation needed]

Heparin and derivative substances

[edit]

Heparin is the most widely used intravenous clinical anticoagulant worldwide.[82] Heparin is a naturally occurring glycosaminoglycan. There are three major categories of heparin: unfractionated heparin (UFH), low molecular weight heparin (LMWH), and ultra-low-molecular weight heparin (ULMWH).[83] Unfractionated heparin is usually derived from pig intestines and bovine lungs.[84] UFH binds to the enzyme inhibitor antithrombin III (AT), causing a conformational change that results in its activation.[85] The activated AT then inactivates factor Xa, thrombin, and other coagulation factors.[86] Heparin can be used in vivo (by injection), and also in vitro to prevent blood or plasma clotting in or on medical devices. In venipuncture, Vacutainer brand blood collecting tubes containing heparin usually have a green cap.[87]

Low molecular weight heparin (LMWH)

[edit]

Low molecular weight heparin (LMWH) is produced through a controlled depolymerization of unfractionated heparin.[83] LMWH exhibits a higher anti-Xa/anti-IIa activity ratio and is useful as it does not require monitoring of the APTT coagulation parameter and has fewer side effects.[83]

Synthetic pentasaccharide inhibitors of factor Xa

[edit]
  • Fondaparinux is a synthetic sugar composed of the five sugars (pentasaccharides) in heparin that bind to antithrombin. It is a smaller molecule than low molecular-weight heparin.
  • Idraparinux
  • Idrabiotaparinux

Direct oral

[edit]

The direct oral anticoagulants (DOACs) were introduced in and after 2008.[88] There are five DOACs currently on the market: dabigatran, rivaroxaban, apixaban, edoxaban and betrixaban.[89] They were also previously referred to as "new/novel" and "non-vitamin K antagonist" oral anticoagulants (NOACs).[90]

Compared to warfarin, DOACs have a rapid onset action and relatively short half-lives; hence, they carry out their function more rapidly and effectively, allowing drugs to reduce their anticoagulation effects quickly.[91] Routine monitoring and dose adjustments of DOACs are less important than for warfarin, as they have better predictable anticoagulation activity.[92] DOAC monitoring, including laboratory monitoring and a complete medication review, should generally be conducted before initiation of a DOAC, 1–3 months after initiation, and then every 6–12 months afterwards.[93]

Both DOACs and warfarin are equivalently effective, but compared to warfarin, DOACs have fewer drug interactions, no known dietary interactions, a wider therapeutic index, and have conventional dosing that does not require dose adjustments with constant monitoring.[94][92] However, there is no countermeasure for most DOACs, unlike for warfarin; nonetheless, the short half-lives of DOACs will allow their effects to recede swiftly. A reversal agent for dabigatran, idarucizumab, is currently available and approved for use by the FDA. Rates of adherence to DOACs are only modestly higher than adherence to warfarin among patients prescribed these drugs. Thus, adherence to anticoagulation is often poor despite hopes that DOACs would lead to higher adherence rates.[95]

DOACs are significantly more expensive than warfarin, but the patients on DOACs may experience reduced lab costs as they do not need to monitor their INR.[93]

Direct factor Xa inhibitors

[edit]
Main article: Direct Xa inhibitor

Drugs such as rivaroxaban, apixaban and edoxaban work by inhibiting factor Xa directly (unlike heparins and fondaparinux, which work via antithrombin activation). Also included in this category are betrixaban from Portola Pharmaceuticals, the discontinued darexaban (YM150) from Astellas, and, more recently, the discontinued letaxaban (TAK-442) from Takeda and eribaxaban (PD0348292) from Pfizer. Betrixaban is significant as it was in 2018, the only oral factor Xa inhibitor approved by the FDA for use in acutely medically ill patients.[96] Darexaban development was discontinued in September 2011; in a trial for prevention of recurrences of myocardial infarction in addition to dual antiplatelet therapy (DAPT), the drug did not demonstrate effectiveness, and the risk of bleeding was increased by approximately 300%.[97] The development of letaxaban for acute coronary syndrome was discontinued in May 2011 following negative results from a Phase II study.[98]

Direct thrombin inhibitors

[edit]
Main article: Direct thrombin inhibitor

Another type of anticoagulant is the direct thrombin inhibitor.[99] Current members of this class include the bivalent drugs hirudin, lepirudin, and bivalirudin and the monovalent drugs argatroban and dabigatran. An oral direct thrombin inhibitor, ximelagatran (Exanta), was denied approval by the Food and Drug Administration (FDA) in September 2004[100] and was pulled from the market entirely in February 2006 after reports of severe liver damage and heart attacks.[101] In November 2010, dabigatran etexilate was approved by the FDA to prevent thrombosis in atrial fibrillation.

Relevance to dental treatments

[edit]

As in any invasive procedure, patients on anticoagulation therapy have an increased risk for bleeding, and caution should be used along with local hemostatic methods to minimize bleeding risk during the operation as well as postoperatively.[102] However, with regards to DOACs and invasive dental treatments, there has not been enough clinical evidence and experience to prove any reliable adverse effects, relevance or interaction between these two.[103] Further clinical prospective studies on DOACs are required to investigate the bleeding risk and hemostasis associated with surgical and dental procedures.[104]

Recommendations of modifications to the usage/dosage of DOACs before dental treatments are made based on the balance of the bleeding risk of each procedure and also the individual's own bleeding risks and renal functionality.[105] With low-bleeding-risk dental procedures, it is recommended that DOACs be continued by the patient to avoid any increase in the risk of a thromboembolic event.[106][107] For dental procedures with a higher risk of bleeding complications (i.e. complex extractions, adjacent extractions leading to a large wound, or more than three extractions), the recommended practice is for the patient to miss or delay a dose of their DOAC before such procedures to minimize the effect on bleeding risk.[108]

Antithrombin protein therapeutics

[edit]

The antithrombin protein is used as a protein therapeutic that can be purified from human plasma[109] or produced recombinantly (for example, Atryn, produced in the milk of genetically modified goats).[110][111]

The FDA approves Antithrombin as an anticoagulant for preventing clots before, during, or after surgery or birthing in patients with hereditary antithrombin deficiency.[109][111]

Other

[edit]

Many other anticoagulants exist in research and development, diagnostics, or as drug candidates.


Reversal agents

[edit]

With the growing number of patients taking oral anticoagulation therapy, studies into reversal agents are gaining increasing interest due to major bleeding events and the need for urgent anticoagulant reversal therapy.[112] Reversal agents for warfarin are more widely studied, and established guidelines for reversal exist due to a longer history of use of warfarin and the ability to get a more accurate measurement of anticoagulation effect in a patient via measuring the INR (International Normalized Ratio).[113] In general, vitamin K is most commonly used to reverse the effect of warfarin in non-urgent settings.[114] However, in urgent settings or settings with extremely high INR (INR >20), hemostatic reversal agents such as fresh frozen plasma (FFP), recombinant factor VIIa, and prothrombin complex concentrate (PCC) have been utilized with proven efficacy.[115] Specifically with warfarin, four-factor PCC (4F-PCC) has been shown to have superior safety and mortality benefits compared to FPP in lowering INR levels.[112]

Although specific antidotes and reversal agents for DOACs are not as widely studied, idarucizumab (for dabigatran) and andexanet alfa (for factor Xa inhibitor) have been used in clinical settings with varying efficacy.[90] Idarucizumab is a monoclonal antibody, approved by the US FDA in 2015, that reverses the effect of dabigatran by binding to both free and thrombin-bound dabigatran.[116][117] Andexanet alfa is a recombinant modified human factor Xa decoy that reverses the effect of factor Xa inhibitors by binding at the active sites of factor Xa inhibitor and making it catalytically inactive.[118][119] Andexanet alfa was approved by the US FDA in 2018.[120] Another drug called ciraparantag, a potential reversal agent for direct factor Xa inhibitors, is still under investigation.[121] Additionally, hemostatic reversal agents have also been used with varying efficacy to reverse the effects of DOACs.[122][123]

Coagulation inhibitor measurement

[edit]

A Bethesda unit (BU) is a measure of blood coagulation inhibitor activity. It is the amount of inhibitor that will inactivate half of a coagulant during the incubation period.[124] It is the standard measure used in the United States and is so named because it was adopted as a standard at a conference in Bethesda, Maryland.[125]

Laboratory use

[edit]

If blood is allowed to clot, laboratory instruments, blood transfusion bags, and medical and surgical equipment will get clogged up and non-operational. In addition, test tubes used for laboratory blood tests will have chemicals added to stop blood clotting. Besides heparin, most of these chemicals bind calcium ions, preventing the coagulation proteins from using them.

  • Ethylenediaminetetraacetic acid (EDTA) strongly and irreversibly chelates (binds) calcium ions, preventing blood from clotting.
  • Citrate is in liquid form in the tube and is used for coagulation tests and blood transfusion bags. It binds calcium but not as strongly as EDTA. The correct proportion of this anticoagulant to blood is crucial because of the dilution, which can be reversed with the addition of calcium. Formulations include plain sodium citrate, acid-citrate-dextrose, and more.
  • Oxalate has a mechanism similar to that of citrate. It is the anticoagulant used in fluoride/oxalate tubes to determine glucose and lactate levels. The fluoride inhibits glycolysis, which can throw off blood sugar measurements. Citrate/fluoride/EDTA tubes work better in this regard.[126]

Dental considerations for long-term users

[edit]

Dental practitioners play an important role in the early detection of anticoagulant overdose through oral manifestations, as the patient does not show any symptoms. Dental treatment of patients taking anticoagulant or antiplatelet medication raises safety concerns in terms of the potential risk of bleeding complications following invasive dental procedures. Therefore, certain guidelines for the dental care of patients taking these drugs are needed.

Detecting overdose

An overdose of anticoagulants usually occurs in people who have heart problems and need to take anticoagulants in the long term to reduce the risk of stroke from their high blood pressure.

An International Normalised Ratio (INR) test would be recommended to confirm the overdose so that the dosage can be adjusted to an acceptable standard. The INR test measures the time it takes for a clot to form in a blood sample relative to a standard.

An INR value of 1 indicates a level of coagulation equivalent to that of an average patient not taking warfarin, and values greater than 1 indicate a longer clotting time and, thus, a longer bleeding time.

Assessing bleeding risk

There are two main parts to the assessment of bleeding risk:

  • Assessment of the likely risk of bleeding associated with the required dental procedure
  • Assessment of the patient's individual-level bleeding risk

Managing bleeding risk

A patient who is on anticoagulants or antiplatelet medications may undergo dental treatments which are unlikely to cause bleeding, such as local anesthesia injection, basic gum charting, removal of plaque, calculus and stain above the gum level, direct or indirect fillings which are above the gingiva, root canal treatment, taking impression for denture or crown and fitting or adjustment of orthodontic appliances.  For all these procedures, it is recommended that the dentist treat the patient following the normal standard procedure and taking care to avoid any bleeding.

For a patient who needs to undergo dental treatments which are more likely to cause bleeding, such as simple tooth extractions (1-3 teeth with small wound size), drainage of swelling inside the mouth, periodontal charting, root planing,  direct or indirect filling which extends below the gingiva, complex filling, flap raising procedure, gingival recontouring and biopsies, the dentist needs to take extra precautions apart from the standard procedure. The recommendations[127] are as follows:

  • if the patient has another medical condition or is taking other medication that may increase bleeding risk, consult the patient's general medical practitioner or specialist
  • if the patient is on a short course of anticoagulant or antiplatelet therapy, delay the non-urgent, invasive procedure until the medication has been discontinued
  • plan treatment for early in the day and week, where possible, to allow time for the management of prolonged bleeding or re-bleeding if it occurs
  • perform the procedure as traumatically as possible, use appropriate local measures and only discharge the patient once hemostasis has been confirmed
  • if travel time to emergency care is a concern, place particular emphasis at the time of the initial treatment on the use of measures to avoid complications
  • advise the patient to take paracetamol, unless contraindicated, for pain relief rather than NSAIDs such as aspirin, ibuprofen, diclofenac or naproxen
  • provide the patient with written post-treatment advice and emergency contact details
  • follow the specific recommendations and advice given for the management of patients taking different anticoagulants or antiplatelet drugs

There is general agreement that in most cases, treatment regimens with older anticoagulants (e.g., warfarin) and antiplatelet agents (e.g., clopidogrel, ticlopidine, prasugrel, ticagrelor, and/or aspirin) should not be altered before dental procedures. The risks of stopping or reducing these medication regimens (i.e., thromboembolism, stroke, myocardial infarction) far outweigh the consequences of prolonged bleeding, which can be controlled with local measures. In patients with other existing medical conditions that can increase the risk of prolonged bleeding after dental treatment or receiving other therapy that can increase bleeding risk, dental practitioners may wish to consult the patient's physician to determine whether care can safely be delivered in a primary care office. Any suggested modification to the medication regimen before dental surgery should be done in consultation and on the advice of the patient's physician.

Based on limited evidence, the consensus appears to be that in most patients who are receiving the newer direct-acting oral anticoagulants (i.e., dabigatran, rivaroxaban, apixaban, or edoxaban) and undergoing dental treatment (in conjunction with usual local measures to control bleeding), no change to the anticoagulant regimen is required. In patients deemed to be at higher risk of bleeding (e.g., patients with other medical conditions or undergoing more extensive procedures associated with higher bleeding risk), consideration may be given, in consultation with and on advice of the patient's physician, to postponing the timing of the daily dose of the anticoagulant until after the procedure; timing the dental intervention as late as possible after last dose of anticoagulant; or temporarily interrupting drug therapy for 24 to 48 hours.

Research

[edit]

A substantial number of compounds are being investigated for use as anticoagulants. The most promising ones act on the contact activation system (factor XIIa and factor XIa); it is anticipated that this may provide agents that prevent thrombosis without conferring a risk of bleeding.[128]

As of November 2021, the direct factor XIa inhibitor milvexian is in Phase II clinical trials for the prevention of an embolism after surgery.[129]

See also

[edit]

References

[edit]
  1. ^ "Overview: Anticoagulant medicines". Health A to Z. NHS. 26 July 2021. Retrieved 2 June 2023.
  2. ^ Azzopardi EA, Whitaker IS, Rozen WM, Naderi N, Kon M (October 2011). "Chemical and mechanical alternatives to leech therapy: a systematic review and critical appraisal". Journal of Reconstructive Microsurgery. 27 (8). Thieme Medical Publishers: 481–6. doi:10.1055/s-0031-1284233. eISSN 0743-684X. PMID 21780018. S2CID 260192613.
  3. ^ Ha YR, Oh SR, Seo ES, Kim BH, Lee DK, Lee SJ (April 2014). "Detection of heparin in the salivary gland and midgut of Aedes togoi". The Korean Journal of Parasitology. 52 (2). The Korean Society for Parasitology and Tropical Medicine: 183–8. doi:10.3347/kjp.2014.52.2.183. eISSN 2982-6799. PMC 4028456. PMID 24850962.
  4. ^ Yoo HH, Nunes-Nogueira VS, Boas, PJ (7 February 2020). "Anticoagulant treatment for subsegmental pulmonary embolism". The Cochrane Database of Systematic Reviews. 2020 (2): CD010222. doi:10.1002/14651858.CD010222.pub4. ISSN 1469-493X. PMC 7004894. PMID 32030721.
  5. ^ Cohen AT, Hamilton M, Mitchell SA, Phatak H, Liu X, Bird A, et al. (2015-12-30). ten Cate H (ed.). "Comparison of the Novel Oral Anticoagulants Apixaban, Dabigatran, Edoxaban, and Rivaroxaban in the Initial and Long-Term Treatment and Prevention of Venous Thromboembolism: Systematic Review and Network Meta-Analysis". PLOS One. 10 (12): e0144856. Bibcode:2015PLoSO..1044856C. doi:10.1371/journal.pone.0144856. PMC 4696796. PMID 26716830.
  6. ^ Almutairi AR, Zhou L, Gellad WF, Lee JK, Slack MK, Martin JR, et al. (July 2017). "Effectiveness and Safety of Non-vitamin K Antagonist Oral Anticoagulants for Atrial Fibrillation and Venous Thromboembolism: A Systematic Review and Meta-analyses". Clinical Therapeutics. 39 (7): 1456–1478.e36. doi:10.1016/j.clinthera.2017.05.358. PMID 28668628.
  7. ^ Banfi G, Salvagno GL, Lippi G (2007-01-01). "The role of ethylenediamine tetraacetic acid (EDTA) as in vitro anticoagulant for diagnostic purposes". Clinical Chemistry and Laboratory Medicine. 45 (5): 565–76. doi:10.1515/CCLM.2007.110. PMID 17484616. S2CID 23824484.
  8. ^ Dobrovolskaia MA, McNeil SE (May 2015). "Safe anticoagulation when heart and lungs are "on vacation"". Annals of Translational Medicine. 3 (Suppl 1): S11. doi:10.3978/j.issn.2305-5839.2015.02.03. PMC 4437941. PMID 26046056.
  9. ^ Pirmohamed M (November 2006). "Warfarin: almost 60 years old and still causing problems". British Journal of Clinical Pharmacology. 62 (5): 509–11. doi:10.1111/j.1365-2125.2006.02806.x. PMC 1885167. PMID 17061959.
  10. ^ Patel S, Singh R, Preuss CV, Patel N (2020). "Warfarin". StatPearls. StatPearls Publishing. PMID 29261922. Retrieved 2020-01-23.
  11. ^ Iqbal AM, Lopez RA, Hai O (2020). "Antiplatelet Medications". StatPearls. StatPearls Publishing. PMID 30725747. Retrieved 2020-01-23.
  12. ^ Harter K, Levine M, Henderson SO (January 2015). "Anticoagulation drug therapy: a review". The Western Journal of Emergency Medicine. 16 (1): 11–7. doi:10.5811/westjem.2014.12.22933. PMC 4307693. PMID 25671002.
  13. ^ Winslow R, Johnson A (2007-12-10). "Race Is on for the Next Blood Thinner". The Wall Street Journal. p. A12. Retrieved 2008-01-06. ...in a market now dominated by one of the oldest mainstay pills in medicine: the blood thinner warfarin. At least five next-generation blood thinners are in advanced testing to treat or prevent potentially debilitating or life-threatening blood clots in surgery and heart patients. First candidates could reach the market in 2009.
  14. ^ Djulbegovic M, Lee AI (September 2018). "An Update on the "Novel" and Direct Oral Anticoagulants, and Long-Term Anticoagulant Therapy". Clinics in Chest Medicine. 39 (3): 583–593. doi:10.1016/j.ccm.2018.04.010. PMID 30122182. S2CID 52039169.
  15. ^ a b Parks AL, Fang MC (July 2017). "Scoring Systems for Estimating the Risk of Anticoagulant-Associated Bleeding". Seminars in Thrombosis and Hemostasis. 43 (5): 514–524. doi:10.1055/s-0037-1598061. PMID 28359135. S2CID 1981707.
  16. ^ Zhu X (February 2017). "The hemorrhage risk of prophylactic external ventricular drain insertion in aneurysmal subarachnoid hemorrhage patients requiring endovascular aneurysm treatment: a systematic review and meta-analysis". Journal of Neurosurgical Sciences. 61 (1): 53–63. doi:10.23736/S0390-5616.16.03244-6. PMID 25963956.
  17. ^ Banerjee K, Poddar K, Mick S, White J, Krishnaswamy A, Johnston D, et al. (November 2017). "Meta-Analysis of Usefulness of Anticoagulation After Transcatheter Aortic Valve Implantation". The American Journal of Cardiology. 120 (9): 1612–1617. doi:10.1016/j.amjcard.2017.07.059. PMID 28844512.
  18. ^ "Blood Thinners". medlineplus.gov. Retrieved 2020-01-23.
  19. ^ Sharma M, Cornelius VR, Patel JP, Davies JG, Molokhia M (July 2015). "Efficacy and Harms of Direct Oral Anticoagulants in the Elderly for Stroke Prevention in Atrial Fibrillation and Secondary Prevention of Venous Thromboembolism: Systematic Review and Meta-Analysis". Circulation. 132 (3): 194–204. doi:10.1161/CIRCULATIONAHA.114.013267. PMC 4765082. PMID 25995317.
  20. ^ Moustafa A, Ruzieh M, Eltahawy E, Karim S (2019). "Antithrombotic therapy in patients with atrial fibrillation and coronary artery disease". Avicenna Journal of Medicine. 9 (4): 123–128. doi:10.4103/ajm.AJM_73_19. PMC 6796304. PMID 31903386.
  21. ^ Kearon C, Akl EA, Ornelas J, Blaivas A, Jimenez D, Bounameaux H, et al. (February 2016). "Antithrombotic Therapy for VTE Disease: CHEST Guideline and Expert Panel Report". Chest. 149 (2): 315–352. doi:10.1016/j.chest.2015.11.026. PMID 26867832.
  22. ^ Kapil N, Datta YH, Alakbarova N, Bershad E, Selim M, Liebeskind DS, et al. (May 2017). "Antiplatelet and Anticoagulant Therapies for Prevention of Ischemic Stroke". Clinical and Applied Thrombosis/Hemostasis. 23 (4): 301–318. doi:10.1177/1076029616660762. PMID 27461564. S2CID 43296498.
  23. ^ Skelley JW, White CW, Thomason AR (January 2017). "The use of direct oral anticoagulants in inherited thrombophilia". Journal of Thrombosis and Thrombolysis. 43 (1): 24–30. doi:10.1007/s11239-016-1428-2. PMID 27734187. S2CID 24650202.
  24. ^ Poli D, Antonucci E, Pengo V, Migliaccio L, Testa S, Lodigiani C, et al. (September 2018). "Mechanical prosthetic heart valves: Quality of anticoagulation and thromboembolic risk. The observational multicenter PLECTRUM study". International Journal of Cardiology. 267: 68–73. doi:10.1016/j.ijcard.2018.04.042. PMID 29957264. S2CID 49588203.
  25. ^ Almony GT, Lefkovits J, Topol EJ (May 1996). "Antiplatelet and anticoagulant use after myocardial infarction". Clinical Cardiology. 19 (5): 357–65. doi:10.1002/clc.4960190506. PMID 8723593. S2CID 103327.
  26. ^ Konstantinides SV, Barco S, Lankeit M, Meyer G (March 2016). "Management of Pulmonary Embolism: An Update". Journal of the American College of Cardiology. 67 (8): 976–90. doi:10.1016/j.jacc.2015.11.061. PMID 26916489.
  27. ^ Dong Z, Zheng J (September 2017). "Anticoagulation after coronary stenting: a systemic review". British Medical Bulletin. 123 (1): 79–89. doi:10.1093/bmb/ldx018. PMID 28910988. S2CID 3800129.
  28. ^ Lander H, Zammert M, FitzGerald D (September 2016). "Anticoagulation management during cross-clamping and bypass". Best Practice & Research. Clinical Anaesthesiology. 30 (3): 359–70. doi:10.1016/j.bpa.2016.07.002. PMID 27650345.
  29. ^ Thomas I, EncisoSilva J, Schlueter M, Greenberg B (2016), Bauersachs J, Butler J, Sandner P (eds.), "Anticoagulation Therapy and NOACs in Heart Failure", Heart Failure, vol. 243, Springer International Publishing, pp. 515–535, doi:10.1007/164_2016_126, ISBN 978-3-319-59658-7, PMID 28233177
  30. ^ Raschi E, Bianchin M, De Ponti R, De Ponti F, Ageno W (June 2017). "Emerging therapeutic uses of direct-acting oral anticoagulants: An evidence-based perspective". Pharmacological Research. 120: 206–218. doi:10.1016/j.phrs.2017.03.026. PMID 28366835. S2CID 36716760.
  31. ^ "HAS-BLED Score for Major Bleeding risk". MDCalc. Retrieved 2014-08-15.
  32. ^ "ATRIA Bleeding Risk". MDCalc. Retrieved 2014-08-15.
  33. ^ "HEMORR₂HAGES Score for Major Bleeding Risk". MDCalc. Retrieved 2020-01-23.
  34. ^ "CHA2DS2-VASc". MDCalc. Retrieved 2014-08-15.
  35. ^ Zhu W, He W, Guo L, Wang X, Hong K (September 2015). "The HAS-BLED Score for Predicting Major Bleeding Risk in Anticoagulated Patients With Atrial Fibrillation: A Systematic Review and Meta-analysis". Clinical Cardiology. 38 (9): 555–61. doi:10.1002/clc.22435. PMC 6490831. PMID 26418409.
  36. ^ Kwan J, Hafdi M, Chiang LL, Myint PK, Wong LS, Quinn TJ (2022-07-13). Cochrane Dementia and Cognitive Improvement Group (ed.). "Antithrombotic therapy to prevent cognitive decline in people with small vessel disease on neuroimaging but without dementia". Cochrane Database of Systematic Reviews. 2022 (7): CD012269. doi:10.1002/14651858.CD012269.pub2. PMC 9281623. PMID 35833913.
  37. ^ Yee J, Kaide CG (August 2019). "Emergency Reversal of Anticoagulation". The Western Journal of Emergency Medicine. 20 (5): 770–783. doi:10.5811/westjem.2018.5.38235. PMC 6754204. PMID 31539334.
  38. ^ Zareh M, Davis A, Henderson S (November 2011). "Reversal of warfarin-induced hemorrhage in the emergency department". The Western Journal of Emergency Medicine. 12 (4): 386–92. doi:10.5811/westjem.2011.3.2051. PMC 3236169. PMID 22224125.
  39. ^ a b Ageno W, Donadini M (November 2018). "Breadth of complications of long-term oral anticoagulant care". Hematology. American Society of Hematology. Education Program. 2018 (1): 432–438. doi:10.1182/asheducation-2018.1.432. PMC 6245998. PMID 30504343.
  40. ^ Ageno W, Mantovani LG, Haas S, Kreutz R, Monje D, Schneider J, et al. (January 2016). "Safety and effectiveness of oral rivaroxaban versus standard anticoagulation for the treatment of symptomatic deep-vein thrombosis (XALIA): an international, prospective, non-interventional study". The Lancet. Haematology. 3 (1): e12-21. doi:10.1016/S2352-3026(15)00257-4. PMID 26765643.
  41. ^ Hylek EM, Evans-Molina C, Shea C, Henault LE, Regan S (May 2007). "Major hemorrhage and tolerability of warfarin in the first year of therapy among elderly patients with atrial fibrillation". Circulation. 115 (21): 2689–96. doi:10.1161/CIRCULATIONAHA.106.653048. PMID 17515465. S2CID 8881388.
  42. ^ Turpie AG, Purdham D, Ciaccia A (September 2017). "Nonvitamin K antagonist oral anticoagulant use in patients with renal impairment". Therapeutic Advances in Cardiovascular Disease. 11 (9): 243–256. doi:10.1177/1753944717714921. PMC 5562140. PMID 28651452.
  43. ^ Weir MR, Kreutz R (October 2018). "Influence of Renal Function on the Pharmacokinetics, Pharmacodynamics, Efficacy, and Safety of Non-Vitamin K Antagonist Oral Anticoagulants". Mayo Clinic Proceedings. 93 (10): 1503–1519. doi:10.1016/j.mayocp.2018.06.018. PMID 30286834. S2CID 52922296.
  44. ^ a b c Kahale LA, Hakoum MB, Tsolakian IG, Matar CF, Barba M, Yosuico VE, et al. (2017-12-29). "Oral anticoagulation in people with cancer who have no therapeutic or prophylactic indication for anticoagulation". Cochrane Database of Systematic Reviews. 12 (12): CD006466. doi:10.1002/14651858.cd006466.pub6. ISSN 1465-1858. PMC 6389337. PMID 29285754.
  45. ^ a b Ageno W, Gallus AS, Wittkowsky A, Crowther M, Hylek EM, Palareti G (February 2012). "Oral anticoagulant therapy: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines". Chest. 141 (2 Suppl): e44S–e88S. doi:10.1378/chest.11-2292. PMC 3278051. PMID 22315269.
  46. ^ Verhagen H (2009-04-24). "Local haemorrhage and necrosis of the skin and underlying tissues, during anti-coagulant therapy with dicumarol or dicumacyl". Acta Medica Scandinavica. 148 (6): 453–67. doi:10.1111/j.0954-6820.1954.tb01741.x. PMID 13171021.
  47. ^ Weinberg AC, Lieskovsky G, McGehee WG, Skinner DG (August 1983). "Warfarin necrosis of the skin and subcutaneous tissue of the male external genitalia". The Journal of Urology. 130 (2): 352–4. doi:10.1016/S0022-5347(17)51147-7. PMID 6876290.
  48. ^ Broekmans AW, Bertina RM, Loeliger EA, Hofmann V, Klingemann HG (June 1983). "Protein C and the development of skin necrosis during anticoagulant therapy". Thrombosis and Haemostasis. 49 (3): 251. doi:10.1055/s-0038-1657378. PMID 6688309. S2CID 38261767.
  49. ^ Grimaudo V, Gueissaz F, Hauert J, Sarraj A, Kruithof EK, Bachmann F (January 1989). "Necrosis of skin induced by coumarin in a patient deficient in protein S". BMJ. 298 (6668): 233–4. doi:10.1136/bmj.298.6668.233. PMC 1835547. PMID 2522326.
  50. ^ Talmadge DB, Spyropoulos AC (May 2003). "Purple toes syndrome associated with warfarin therapy in a patient with antiphospholipid syndrome". Pharmacotherapy. 23 (5): 674–7. doi:10.1592/phco.23.5.674.32200. PMID 12741443. S2CID 28632135.
  51. ^ Raj K, Collins B, Rangarajan S (September 2001). "Purple toe syndrome following anticoagulant therapy". British Journal of Haematology. 114 (4): 740. doi:10.1046/j.1365-2141.2001.03107.x. PMID 11564060. S2CID 20482173.
  52. ^ Adams J, Pepping J (August 2005). "Vitamin K in the treatment and prevention of osteoporosis and arterial calcification" (PDF). American Journal of Health-System Pharmacy. 62 (15): 1574–81. doi:10.2146/ajhp040357. PMID 16030366.
  53. ^ Danziger J (September 2008). "Vitamin K-dependent proteins, warfarin, and vascular calcification". Clinical Journal of the American Society of Nephrology. 3 (5): 1504–10. doi:10.2215/CJN.00770208. PMC 4571144. PMID 18495950.
  54. ^ Pettifor JM, Benson R (March 1975). "Congenital malformations associated with the administration of oral anticoagulants during pregnancy". The Journal of Pediatrics. 86 (3): 459–62. doi:10.1016/S0022-3476(75)80986-3. PMID 1113236.
  55. ^ Hall JG, Pauli RM, Wilson KM (January 1980). "Maternal and fetal sequelae of anticoagulation during pregnancy". The American Journal of Medicine. 68 (1): 122–40. doi:10.1016/0002-9343(80)90181-3. PMID 6985765.
  56. ^ Gage BF, Birman-Deych E, Radford MJ, Nilasena DS, Binder EF (January 2006). "Risk of osteoporotic fracture in elderly patients taking warfarin: results from the National Registry of Atrial Fibrillation 2". Archives of Internal Medicine. 166 (2): 241–6. doi:10.1001/archinte.166.2.241. PMID 16432096.
  57. ^ a b Baroletti SA, Goldhaber SZ (August 2006). "Heparin-induced thrombocytopenia". Circulation. 114 (8): e355-6. doi:10.1161/CIRCULATIONAHA.106.632653. PMID 16923760.
  58. ^ Warkentin TE, Greinacher A, Koster A, Lincoff AM (June 2008). "Treatment and prevention of heparin-induced thrombocytopenia: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition)". Chest. 133 (6 Suppl): 340S–380S. doi:10.1378/chest.08-0677. PMID 18574270.
  59. ^ Linkins LA, Hu G, Warkentin TE (October 2018). "Systematic review of fondaparinux for heparin-induced thrombocytopenia: When there are no randomized controlled trials". Research and Practice in Thrombosis and Haemostasis. 2 (4): 678–683. doi:10.1002/rth2.12145. PMC 6178656. PMID 30349886.
  60. ^ Wittkowsky AK (September 2001). "Drug interactions update: drugs, herbs, and oral anticoagulation". Journal of Thrombosis and Thrombolysis. 12 (1): 67–71. doi:10.1023/A:1012742628628. PMID 11711691. S2CID 22447084.
  61. ^ Rui TQ, Zhang L, Qiao HZ, Huang P, Qian S, Li JS, et al. (January 2016). "Preparation and Physicochemical and Pharmacokinetic Characterization of Ginkgo Lactone Nanosuspensions for Antiplatelet Aggregation". Journal of Pharmaceutical Sciences. 105 (1): 242–249. doi:10.1016/j.xphs.2015.10.002. PMID 26852855.
  62. ^ Yun YP, Do JH, Ko SR, Ryu SY, Kim JH, Song HC, et al. (October 2001). "Effects of Korean red ginseng and its mixed prescription on the high molecular weight dextran-induced blood stasis in rats and human platelet aggregation". Journal of Ethnopharmacology. 77 (2–3): 259–264. doi:10.1016/S0378-8741(01)00303-8. PMID 11535373.
  63. ^ Choi S, Oh DS, Jerng UM (2017-08-10). Borrelli F (ed.). "A systematic review of the pharmacokinetic and pharmacodynamic interactions of herbal medicine with warfarin". PLOS ONE. 12 (8): e0182794. Bibcode:2017PLoSO..1282794C. doi:10.1371/journal.pone.0182794. ISSN 1932-6203. PMC 5552262. PMID 28797065.
  64. ^ Kurnik D, Lubetsky A, Loebstein R, Almog S, Halkin H (November 2003). "Multivitamin Supplements May Affect Warfarin Anticoagulation in Susceptible Patients". Annals of Pharmacotherapy. 37 (11): 1603–1606. doi:10.1345/aph.1D102. ISSN 1060-0280. PMID 14565795. S2CID 43777757.
  65. ^ Harder S, Thürmann P (June 1996). "Clinically Important Drug Interactions with Anticoagulants: An Update". Clinical Pharmacokinetics. 30 (6): 416–444. doi:10.2165/00003088-199630060-00002. ISSN 0312-5963. PMID 8792056. S2CID 22389544.
  66. ^ Lippi G, Mattiuzzi C, Franchini M (April 2016). "Vegetables intake and venous thromboembolism: a systematic review". Blood Coagulation & Fibrinolysis. 27 (3): 242–245. doi:10.1097/MBC.0000000000000427. ISSN 0957-5235. PMID 27023878. S2CID 33380206.
  67. ^ "Avocado: Health Benefits, Uses, Side Effects, Dosage & Interactions". RxList. Retrieved 2020-01-23.
  68. ^ Dentali F, Crowther M, Galli M, Pomero F, Garcia D, Clark N, et al. (2016-05-27). "Effect of Vitamin K Intake on the Stability of Treatment with Vitamin K Antagonists: A Systematic Review of the Literature". Seminars in Thrombosis and Hemostasis. 42 (6): 671–681. doi:10.1055/s-0036-1581105. ISSN 0094-6176. PMID 27232386. S2CID 24822900.
  69. ^ "Warfarin Uses, Dosage, Side Effects". Drugs.com. Retrieved 2020-01-23.
  70. ^ Sullivan DM, Ford MA, Boyden TW (1998-08-01). "Grapefruit juice and the response to warfarin". American Journal of Health-System Pharmacy. 55 (15): 1581–1583. doi:10.1093/ajhp/55.15.1581. ISSN 1079-2082. PMID 9706183.
  71. ^ Di Nisio M, van Es N, Büller HR (December 2016). "Deep vein thrombosis and pulmonary embolism". The Lancet. 388 (10063): 3060–3073. doi:10.1016/S0140-6736(16)30514-1. PMID 27375038. S2CID 25712161.
  72. ^ Koehl JL, Hayes BD, Al-Samkari H, Rosovsky R (2020-01-23). "A comprehensive evaluation of apixaban in the treatment of venous thromboembolism". Expert Review of Hematology. 13 (2): 155–173. doi:10.1080/17474086.2020.1711731. ISSN 1747-4086. PMID 31958251. S2CID 210842354.
  73. ^ a b American Physical Therapy Association (15 September 2014), "Five Things Physicians and Patients Should Question", Choosing Wisely: an initiative of the ABIM Foundation, American Physical Therapy Association, retrieved 15 September 2014, which cites
  74. ^ Di Minno A, Frigerio B, Spadarella G, Ravani A, Sansaro D, Amato M, et al. (July 2017). "Old and new oral anticoagulants: Food, herbal medicines and drug interactions". Blood Reviews. 31 (4): 193–203. doi:10.1016/j.blre.2017.02.001. hdl:2434/476466. PMID 28196633.
  75. ^ Almarshad F, Alaklabi A, Bakhsh E, Pathan A, Almegren M (December 2018). "Use of direct oral anticoagulants in daily practice". American Journal of Blood Research. 8 (4): 57–72. PMC 6334188. PMID 30697449.
  76. ^ Verdecchia P, Angeli F, Aita A, Bartolini C, Reboldi G (April 2016). "Why switch from warfarin to NOACs?". Internal and Emergency Medicine. 11 (3): 289–293. doi:10.1007/s11739-016-1411-0. ISSN 1828-0447. PMID 26972708. S2CID 25807727.
  77. ^ Diener HC, Ntaios G, O'Donnell M, Easton JD (2018-09-22). "Non-vitamin-K oral anticoagulants (NOACs) for the prevention of secondary stroke". Expert Opinion on Pharmacotherapy. 19 (14): 1597–1602. doi:10.1080/14656566.2018.1515913. ISSN 1465-6566. PMID 30152249. S2CID 52099757.
  78. ^ Pol D, Curtis C, Ramkumar S, Bittinger L (April 2019). "NOACs Now Mainstream for the Use of Anticoagulation in Non-Valvular Atrial Fibrillation in Australia". Heart, Lung and Circulation. 28 (4): e40–e42. doi:10.1016/j.hlc.2018.03.010. PMID 29861320. S2CID 44103560.
  79. ^ Werdan K, Braun-Dullaeus R, Presek P (August 2013). "Anticoagulation in atrial fibrillation: NOAC's the word". Deutsches Ärzteblatt International. 110 (31–32): 523–4. doi:10.3238/arztebl.2013.0523. PMC 3782018. PMID 24069072. Things have changed dramatically with the introduction of the new oral anticoagulants (NOACs) — dabigatran, a factor IIa (thrombin) inhibitor, and the factor Xa inhibitors rivaroxaban and apixaban. Clinical trials have shown them therapeutically superior, or at least non-inferior, to VKAs, with less serious side effects.
  80. ^ Heine GH, Brandenburg V, Schirmer SH (2018-04-27). "Orale Antikoagulation bei chronischer Nierenerkrankung und Vorhofflimmern". Deutsches Ärzteblatt Online. 115 (17): 287–294. doi:10.3238/arztebl.2018.0287. ISSN 1866-0452. PMC 5974258. PMID 29789105.
  81. ^ Efird LE, Chasler J, Alexander GC, McGuire M (Jun 21, 2016). "Prescribing Patterns of Novel Anticoagulants Within a Statewide Multispecialty Practice". American Journal of Pharmacy Benefits. 8 (3): 97–102.
  82. ^ Linhardt RJ (June 2003). "2003 Claude S. Hudson Award address in carbohydrate chemistry. Heparin: structure and activity". Journal of Medicinal Chemistry. 46 (13): 2551–64. doi:10.1021/jm030176m. PMID 12801218.
  83. ^ a b c Onishi A, St Ange K, Dordick JS, Linhardt RJ (June 2016). "Heparin and anticoagulation". Frontiers in Bioscience. 21 (7): 1372–92. doi:10.2741/4462. PMID 27100512.
  84. ^ Casu B, Naggi A, Torri G (February 2015). "Re-visiting the structure of heparin". Carbohydrate Research. 403: 60–8. doi:10.1016/j.carres.2014.06.023. PMID 25088334.
  85. ^ Seo Y, Andaya A, Leary JA (March 2012). "Preparation, separation, and conformational analysis of differentially sulfated heparin octasaccharide isomers using ion mobility mass spectrometry". Analytical Chemistry. 84 (5): 2416–23. doi:10.1021/ac203190k. PMC 3296823. PMID 22283665.
  86. ^ Allingstrup M, Wetterslev J, Ravn FB, Møller AM, Afshari A (April 2016). "Antithrombin III for critically ill patients: a systematic review with meta-analysis and trial sequential analysis". Intensive Care Medicine. 42 (4): 505–520. doi:10.1007/s00134-016-4225-7. PMC 2137061. PMID 26862016.
  87. ^ Brizzee L, Stone A, Palmer MC (May 2020). "False lithium toxicity secondary to lithium heparin test tube: A case report and review". Ment Health Clin. 10 (3): 90–94. doi:10.9740/mhc.2020.05.090. PMC 7213950. PMID 32420006.
  88. ^ "Human medicines European public assessment report (EPAR): Pradaxa, dabigatran etexilate, Arthroplasty, Replacement,Venous Thromboembolism, Date of authorisation: 17/03/2008, Revision: 29, Status: Authorised". Case Medical Research. 2019-07-16. doi:10.31525/cmr-1321569. ISSN 2643-4652. S2CID 241319098.
  89. ^ Douxfils J, Ageno W, Samama CM, Lessire S, Ten Cate H, Verhamme P, et al. (February 2018). "Laboratory testing in patients treated with direct oral anticoagulants: a practical guide for clinicians". Journal of Thrombosis and Haemostasis. 16 (2): 209–219. doi:10.1111/jth.13912. PMID 29193737. S2CID 46865986.
  90. ^ a b Udayachalerm S, Rattanasiri S, Angkananard T, Attia J, Sansanayudh N, Thakkinstian A (September 2018). "The Reversal of Bleeding Caused by New Oral Anticoagulants (NOACs): A Systematic Review and Meta-Analysis". Clinical and Applied Thrombosis/Hemostasis. 24 (9_suppl): 117S–126S. doi:10.1177/1076029618796339. PMC 6714855. PMID 30176738.
  91. ^ "Management of Dental Patients Taking Anticoagulants or Antiplatelet Drugs" (PDF). Scottish Dental Clinical Effectiveness Programme. August 2015. Archived from the original (PDF) on 2017-03-28. Retrieved 2016-03-09.
  92. ^ a b Clark NP (November 2018). "Role of the anticoagulant monitoring service in 2018: beyond warfarin". Hematology. American Society of Hematology. Education Program. 2018 (1): 348–352. doi:10.1182/asheducation-2018.1.348. PMC 6246023. PMID 30504331.
  93. ^ a b Chen A, Stecker E, A Warden B (2020-06-15). "Direct Oral Anticoagulant Use: A Practical Guide to Common Clinical Challenges". Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease. 9 (13): e017559. doi:10.1161/JAHA.120.017559. ISSN 2047-9980. PMC 7670541. PMID 32538234.
  94. ^ "Novel anticoagulants". Heart Matters Magazine. British Heart Foundation. Archived from the original on 2017-10-26. Retrieved 2016-03-09.
  95. ^ Ozaki AF, Choi AS, Le QT, Ko DT, Han JK, Park SS, et al. (2020). "Real-World Adherence and Persistence to Direct Oral Anticoagulants in Patients With Atrial Fibrillation: A Systematic Review and Meta-Analysis". Circulation: Cardiovascular Quality and Outcomes. 13 (3): e005969. doi:10.1161/CIRCOUTCOMES.119.005969. ISSN 1941-7705. PMID 32148102. S2CID 212640015.
  96. ^ Lekura J, Kalus JS (August 2018). "Overview of betrixaban and its role in clinical practice". American Journal of Health-System Pharmacy. 75 (15): 1095–1102. doi:10.2146/ajhp170785. PMID 29941506. S2CID 49418996.
  97. ^ Steg PG, Mehta SR, Jukema JW, Lip GY, Gibson CM, Kovar F, et al. (October 2011). "RUBY-1: a randomized, double-blind, placebo-controlled trial of the safety and tolerability of the novel oral factor Xa inhibitor darexaban (YM150) following acute coronary syndrome". European Heart Journal. 32 (20): 2541–54. doi:10.1093/eurheartj/ehr334. PMC 3295208. PMID 21878434.
  98. ^ Dwyer J, Walsh C (May 2013). "First Time European Approval for Xarelto in ACS". Decision Resources. Archived from the original on 2014-07-19.
  99. ^ Di Nisio M, Middeldorp S, Büller HR (September 2005). "Direct thrombin inhibitors" (PDF). The New England Journal of Medicine. 353 (10): 1028–40. doi:10.1056/NEJMra044440. PMID 16148288.
  100. ^ "Exanta". Ask Dr. Stephan Moll. The Thrombophilia Awareness Project. Archived from the original on 25 May 2011.
  101. ^ "Exanta™ (ximelagatran) Study report summaries". AstraZeneca Clinical Trials. Archived from the original on 2006-03-18.
  102. ^ Manfredi M, Dave B, Percudani D, Christoforou J, Karasneh J, Diz Dios P, et al. (June 2019). "World workshop on oral medicine VII: Direct anticoagulant agents management for invasive oral procedures: A systematic review and meta-analysis". Oral Diseases. 25 (S1): 157–173. doi:10.1111/odi.13086. PMID 31140701. S2CID 169034257.
  103. ^ Bensi C, Belli S, Paradiso D, Lomurno G (July 2018). "Postoperative bleeding risk of direct oral anticoagulants after oral surgery procedures: a systematic review and meta-analysis". International Journal of Oral and Maxillofacial Surgery. 47 (7): 923–932. doi:10.1016/j.ijom.2018.03.016. PMID 29627150. S2CID 4697607.
  104. ^ Costantinides F, Rizzo R, Pascazio L, Maglione M (January 2016). "Managing patients taking novel oral anticoagulants (NOAs) in dentistry: a discussion paper on clinical implications". BMC Oral Health. 16: 5. doi:10.1186/s12903-016-0170-7. PMC 4731944. PMID 26822674.
  105. ^ Kosyfaki P, Att W, Strub JR (August 2011). "The dental patient on oral anticoagulant medication: a literature review". Journal of Oral Rehabilitation. 38 (8): 615–33. doi:10.1111/j.1365-2842.2010.02184.x. PMID 21073495.
  106. ^ van Diermen DE, van der Waal I, Hoogstraten J (December 2013). "Management recommendations for invasive dental treatment in patients using oral antithrombotic medication, including novel oral anticoagulants". Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 116 (6): 709–16. doi:10.1016/j.oooo.2013.07.026. PMID 24120910.
  107. ^ Shi Q, Xu J, Zhang T, Zhang B, Liu H (2017-02-08). "Post-operative Bleeding Risk in Dental Surgery for Patients on Oral Anticoagulant Therapy: A Meta-analysis of Observational Studies". Frontiers in Pharmacology. 8: 58. doi:10.3389/fphar.2017.00058. PMC 5296357. PMID 28228727.
  108. ^ "Management of Dental Patients Taking Anticoagulants or Antiplatelet Drugs: Dental Clinical Guidance" (PDF). Scottish Dental Clinical Effectiveness Programme. Archived from the original (PDF) on 2017-03-28. Retrieved 2020-01-09.
  109. ^ a b "Thrombate III label" (PDF). Archived from the original (PDF) on 2012-11-15.
  110. ^ Center for Biologics Evaluation and Research (24 April 2019). "Fractionated Plasma Products - ATryn". www.fda.gov.
  111. ^ a b "Antithrombin (Recombinant) US Package Insert ATryn for Injection February 3, 2009" (PDF). Food and Drug Administration.
  112. ^ a b Tornkvist M, Smith JG, Labaf A (February 2018). "Current evidence of oral anticoagulant reversal: A systematic review". Thrombosis Research. 162: 22–31. doi:10.1016/j.thromres.2017.12.003. PMID 29258056.
  113. ^ Hanley JP (2004-11-01). "Warfarin reversal". Journal of Clinical Pathology. 57 (11): 1132–1139. doi:10.1136/jcp.2003.008904. ISSN 0021-9746. PMC 1770479. PMID 15509671.
  114. ^ Makris M, Greaves M, Phillips WS, Kitchen S, Rosendaal FR, Preston EF (March 1997). "Emergency oral anticoagulant reversal: the relative efficacy of infusions of fresh frozen plasma and clotting factor concentrate on correction of the coagulopathy". Thrombosis and Haemostasis. 77 (3): 477–480. doi:10.1055/s-0038-1655992. ISSN 0340-6245. PMID 9065997. S2CID 45458169.
  115. ^ Chai-Adisaksopha C, Hillis C, Siegal DM, Movilla R, Heddle N, Iorio A, et al. (September 2016). "Prothrombin complex concentrates versus fresh frozen plasma for warfarin reversal A systematic review and meta-analysis". Thrombosis and Haemostasis. 116 (11): 879–890. doi:10.1160/TH16-04-0266. ISSN 0340-6245. PMID 27488143. S2CID 4733615.
  116. ^ Pakraftar S (2014). "Dabigatran etixilate and traumatic brain injury: Evolving anticoagulants require evolving care plans". World Journal of Clinical Cases. 2 (8): 362–6. doi:10.12998/wjcc.v2.i8.362. ISSN 2307-8960. PMC 4133427. PMID 25133148.
  117. ^ Ryn Jv, Stangier J, Haertter S, Liesenfeld KH, Wienen W, Feuring M, et al. (2010). "Dabigatran etexilate – a novel, reversible, oral direct thrombin inhibitor: Interpretation of coagulation assays and reversal of anticoagulant activity". Thrombosis and Haemostasis. 103 (6): 1116–1127. doi:10.1160/TH09-11-0758. ISSN 0340-6245. PMID 20352166. S2CID 37404563.
  118. ^ Siegal DM, Curnutte JT, Connolly SJ, Lu G, Conley PB, Wiens BL, et al. (2015-12-17). "Andexanet Alfa for the Reversal of Factor Xa Inhibitor Activity". New England Journal of Medicine. 373 (25): 2413–2424. doi:10.1056/NEJMoa1510991. ISSN 0028-4793. PMID 26559317.
  119. ^ Connolly SJ, Milling TJ, Eikelboom JW, Gibson CM, Curnutte JT, Gold A, et al. (2016-09-22). "Andexanet Alfa for Acute Major Bleeding Associated with Factor Xa Inhibitors". New England Journal of Medicine. 375 (12): 1131–1141. doi:10.1056/NEJMoa1607887. ISSN 0028-4793. PMC 5568772. PMID 27573206.
  120. ^ Reed M, Tadi P, Nicolas D (2020), "Andexanet Alfa", StatPearls, StatPearls Publishing, PMID 30137783, retrieved 2020-01-23
  121. ^ Ansell JE, Bakhru SH, Laulicht BE, Steiner SS, Grosso MA, Brown K, et al. (February 2017). "Single-dose ciraparantag safely and completely reverses anticoagulant effects of edoxaban". Thrombosis and Haemostasis. 117 (2): 238–245. doi:10.1160/TH16-03-0224. ISSN 0340-6245. PMC 6260118. PMID 27853809.
  122. ^ Eerenberg ES, Kamphuisen PW, Sijpkens MK, Meijers JC, Buller HR, Levi M (2011-10-04). "Reversal of Rivaroxaban and Dabigatran by Prothrombin Complex Concentrate: A Randomized, Placebo-Controlled, Crossover Study in Healthy Subjects". Circulation. 124 (14): 1573–1579. doi:10.1161/CIRCULATIONAHA.111.029017. ISSN 0009-7322. PMID 21900088. S2CID 961167.
  123. ^ Marlu R, Hodaj E, Paris A, Albaladejo P, Crackowski J, Pernod G (2012). "Effect of non-specific reversal agents on anticoagulant activity of dabigatran and rivaroxaban: A randomised crossover ex vivo study in healthy volunteers". Thrombosis and Haemostasis. 108 (8): 217–224. doi:10.1160/TH12-03-0179. ISSN 0340-6245. PMID 22627883. S2CID 28694620.
  124. ^ "Bethesda unit". Biology Online. Retrieved 2009-02-14.
  125. ^ Schumacher HR (2000). Handbook of Hematologic Pathology. Informa Health Care. p. 583. ISBN 978-0-8247-0170-3.
  126. ^ Norman M, Jones I (May 2014). "The shift from fluoride/oxalate to acid citrate/fluoride blood collection tubes for glucose testing — The impact upon patient results". Clinical Biochemistry. 47 (7–8): 683–685. doi:10.1016/j.clinbiochem.2014.01.011. PMID 24463230.
  127. ^ "Management of Dental Patients Taking Anticoagulants or Antiplatelet Drugs – New guidance from SDCEP | Scottish Dental". 15 September 2015. Retrieved 2020-02-20.
  128. ^ Fredenburgh JC, Weitz JI (12 October 2020). "New Anticoagulants: Moving Beyond the Direct Oral Anticoagulants". Journal of Thrombosis and Haemostasis. 19 (1): 20–29. doi:10.1111/jth.15126. PMID 33047462. S2CID 222320654.
  129. ^ Weitz JI, Strony J, Ageno W, Gailani D, Hylek EM, Lassen MR, et al. (November 2021). "Milvexian for the Prevention of Venous Thromboembolism". The New England Journal of Medicine. 385 (23): 2161–2172. doi:10.1056/NEJMoa2113194. PMC 9540352. PMID 34780683. S2CID 244132392.
[edit]
Retrieved from "https://en.wikipedia.org/w/index.php?title=Anticoagulant&oldid=1253673333#Types"