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Effective Management Strategies for Dental Patients on Anticoagulants: Ensuring Optimal Care and Patient Safety: An Overview

Corresponding author: Melody Kh Th Chiru, Department of Oral Medicine and Radiology, Sathyabama Dental College, Tamil Nadu, India. drmelodykh@gmail.com
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Received: ,
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How to cite this article: TH Chiru DK, Baskar RB, C PC, K SV. Effective Management Strategies for Dental Patients on Anticoagulants: Ensuring Optimal Care and Patient Safety: An Overview. Dent J Indira Gandhi Int Med Sci. doi: 10.25259/DJIGIMS_20_2024
Abstract
Anticoagulants are essential for healing damaged blood arteries because they prevent blood from clotting. They disrupt the body’s normal balance and reduce the risk of thromboembolic episodes. For many illnesses and medical problems, extended therapy for four weeks or more is necessary. Some research has compared the risk of continuing anticoagulant medication with bleeding and embolic consequences in patients on anticoagulants. Patients with a therapeutic INR of less than 4 are more likely to continue taking anticoagulants, which carry a 1% risk of serious embolic consequences compared to a 0.2% chance of major bleeding. Therefore, individuals taking dabigatran, rivaroxaban, or apixaban should consult their treating physician before having dental work done. When treating patients using anticoagulants, dentists and doctors should collaborate to ensure that the patient’s INR is within the therapeutic range.
Keywords
Deep vein thrombosis
Direct thrombin inhibitors
Pulmonary embolism
Venous-thromboembolism
INTRODUCTION
Anticoagulants with unique pharmacological properties or mechanisms that work are crucial for treating various thromboembolic diseases.Considering the chemical characteristics of such substances is essential for optimizing perioperative procedures, particularly in dentistry. This methodical research focuses on the problem of reducing hemorrhage risks among individuals receiving dental treatment while using coagulant medication. Dental professionals, nevertheless, have difficulties or often refer the patients using such medicines to experts,even for simple procedures, despite their safety. Extended hemorrhage and bruises are common side effects that deter clinicians from handling individuals on thrombotic medications but avoiding anticoagulant/antiplatelet drugs can increasethe likelihoodof developing blood clots,which can lead to cardiac arrest stroke or blood clots.Thus, it is necessary to establish a balance between the medicines to ensure the consideration of the possibility of bleeding and the dangers of discontinuing or lowering these medications.
These medicines are divided into three groups: vitamin K antagonists, which include warfarin, acenocoumarol, and phenprocoumon; low-molecular-weight heparin (LMWH); and unfractionated heparin (UFH). These anticoagulants, which are widely utilised though they have been around for 50 years, effectively manage blood coagulation when taken as directed. Both UFH and warfarin function distinctly within the coagulation process, and their medical experience challenges newer anticoagulants that were produced more recently. It is important to note that this older medicine is generally safe to use, provided that bleeding levels are regularly monitored and the appropriate dosages are administered.[1] The probable advantages of warfarin, one of its most prescribed and proven clotting agents for minimising thromboembolic episodes, are uncertain, and issues may occur if the drug is stopped before routine surgical procedures. Warfarin sodium, a suggested therapy for cardiovascular problems, also inhibits vitamin K activation by interfering with the clotting pathway. The usual starting dose is 4-5 mg daily, and the tablet strength ranges from 1 to 10 mg. Warfarin's sluggish onset, unexpected variability, and narrow therapeutic range make it difficult to maintain.[2] Researchers have discovered that if an individual's International Normalised Ratio (INR) exceeds 3.5 on the day before surgery, they may require basic teeth extractions with potential blood loss.[3] Heparins are widely accessible and approved to prevent thrombin and other commonly administered anticoagulant therapies, which include antithrombotic medications like bivalirudin and Lepirudin, two other immediate drugs are therefore only authorised to treat thrombotic consequences of heparin-induced.[4] Clinical investigations have indicated an advisable dosage of 150 mg per day or 220 mg once daily, or 150 mg and 110 mg each day, producing a significant plasma level over 2-3 hours.[5]
Novel oral anticoagulants (NOACs) offer advantages comparable to those of conventional blood thinners, particularly in situations where continuous monitoring or maintaining therapeutic effectiveness is less critical. They may be considered as alternatives for patients on warfarin who struggle to maintain an adequate INR. Since NOACs have relatively short half-lives, they must be discontinued before procedures to minimize bleeding risk or to allow drug clearance. As NOACs can interact with food and other medications, adherence to the prescribed dosing regimen is recommended, although routine monitoring is generally not required.[6] Numerous thorough studies have shown the health benefits and usefulness of NOACs. Despite its benefits, healthcare providers must exercise caution while administering these drugs to some patient groups, such as the elderly, people with liver or kidney diseases, people with a relatively low body mass index (BMI), or people who have experienced bleeding episodes in the past.
Dabigatran etexilate (Pradaxa), which can be metabolized by esterase and has a 14-17-hour half-life, must be administered orally and taken twice daily. It has a 6% bioavailability. For those with a creatinine elimination rate of 30 mL/min, 150 mg given orally twice daily is suggested. For individuals with a creatinine clearance of 15-30 mL/min,the ideal amount is 75 mg twice daily.[7] It is a good substitute for warfarin because it is effective and safer. With no need to change dosages or be on the lookout for hemorrhage, particularly in situations with major tooth extraction, dentists ought to seek a doctor's advice before performing any dental treatments.[8]
Argatrobanis a strong substance that changeably attaches itself to coagulation or fibrinogen, which the liver metabolises. Its excretion is decreased in significant liver dysfunction, necessitating a dosage reduction it is not suggested if significant liver failure although inadequate kidney function does not necessitate modification the main adverse effect is bleeding which is controlled by halting the infusion and using supportive care because there is not a specific counteragent the anticoagulants impact of this medication wears off in 2 to 4 hours after the injection stops in the individual with common liver function still it can last up to 24 hours in individuals with the liver disability when used with warfarin argatroban can cause problems by extending PT/INR past normal limits and making dose changes more difficult.[9]
Apixaban is an effective and reversible activator of Factor Xa, a protein that acts neither independently nor linked to prothrombinase. It has a bioavailability through the oral cavity of more than 50%, a 12-hour terminal life span, and peak levels in the blood that occur 1-3 and 4 hours post ingestion. Although 75% of apixaban is processed by the liver, mostly by cytochrome P450 3A4 and CYP-independent processes, only 25% of it is removed renally, in contrast with different anticoagulant medications. In those with atrial fibrillation, it finds use in treating acute venous thromboembolism, reducing strokes or widespread embolism, treating venous thromboembolism after major orthopaedic procedures, and providing additional safeguards in ischemic heart disease.[10]
Rivaroxabanis a factor X inhibitor that relies on dosage for its effectiveness. It has two methods of elimination, with two-thirds of the distributed dose being released in the urine and the remaining one-third being excreted through feces.[11] Following 21 days, the basic intake is 15 mg twice a day, and during prolonged treatment and problem-preventative measures, the dose is raised to 20 mg once daily.[12] For this drug, a dosage of just one daily is advised. During routine dental procedures, a missed morning dose can be taken the following day to manage the bleeding. However, if at least 4 hours have passed since the last dose was administered, individuals who missed it should take it that same evening before getting any dental work done.[13]
Edoxaban inhibits Factor Xa directly after going through many elimination routes; three-quarters of it is excreted in the urine, and about 70% is excreted unaltered.[14]
With an average period of 9-11 hours and peak plasma levels throughout the first 1-2 hours of treatment, the FDA approved it in 2015. According to Curto et al. (2016), individuals using the medicine did not need blood coagulation surveillance, and simple tooth extractions should not interfere with the medication.[15]According to studies, people using more recent oral anticoagulants should have their bleeding causes associated with dentistry or other oral treatments assessed because the low risk of hemorrhage may not necessitate stopping the prescription.[16] Therefore, before undertaking dental operations, people of all ages, notably older ones, should thoroughly assess their condition and consider other physiological factors.
Evaluation of laboratory investigations:
It is essential to exercise prudence whenever switching from warfarin to LMWH, since the need for anticoagulation or the true cause of blood formation may not support the decision to stop using warfarin. Switching to heparin may cause thrombocytopenia that may impair the capacity to bind blood in the future.[17] In the near term, dental treatment with significant anticoagulation can be resumed with an INR target of 30 to 40, in addition to the use of antifibrinolytics for prophylaxis.The primary purpose of the prothrombin time (PT) evaluation was to assess the effectiveness of the widely used and optional routes of blood coagulation.The PT assessment has an average score of 10 to 15 seconds, however, the PT test may not be accurate or dependable for several reasons. The time it takes for blood to coagulate while combining calcium and plasma, which has been citrated by thromboplastin, is measured.[18]
Bleeding time (BT). In 1910, the bleeding time (BT) test emerged as a way of analyzing the activity of plaque. It is frequently used to look for possible bleeds during pre-surgical examinations.[19] Normally, the BT ranges from 3 to 6 minutes. Prolonged BT is characteristic of features such as purpura; however, a study showed that patients taking aspirin may have elevated BT during pre-surgical blood loss.[20]According to the study, a markedly long-term BT might not always result in substantial loss of blood when surgery is performed. Gathering blood in a sterile glass test tube and gently tilting it every 30 seconds before a clot formsis the conventional procedure for calculating blood clotting time. Although more precise methods, including several test tubes, have been developed, the duration of clotting is not frequently utilized in clinics due to the substantial variance based on the measuring method. Rather, it is more common to assess clotting variables utilizing complex chemical processes.[21]
Clotting time is the most popular method to determine the duration it takes for a clotting agent to form. Take blood in a sterile glass test container and turn it gently at regular intervals until a clump forms. With this approach, the average time required for clotting ranges from 6 to 10 minutes for accurate results. Although more precise methods using many test tubes have been developed, blood clotting time is no longer frequently used in clinics due to significant variation depending on the measurement technique; instead, it is better to assess clotting components using intricate chemical processes.[22]
Evaluation of bleeding risk:
Although complex situations involving those receiving blood-thinning therapy were uncommon, clinicians could be worried about slight adverse reactions like excessive or constant hemorrhage, which are usually manageable with initial hemostasis.[23]According toadditional research, using LMWH drugs can help reduce the probability of bleeding. It is crucial to consider the possibility of hemorrhaging during high-risk oral procedures, such as substantial procedures, tooth implantation, or bone transplant treatments, and to halt anticoagulant therapy temporarily.[24]
We may enhance individual shielding or get more precise analytical results by keeping dental experts and medical specialists closely connected and working together. Significant bleeding issues can also be avoided by carefully reviewing the patient's condition and undergoing necessary tests.
The bleeding risk associated with alternative medications:
Due to their interference accompanied by vitamin K metabolism, certain antibiotics, including metronidazole, erythromycin, cephalosporins, and antifungal drugs, may elevate the risk of hemorrhage,which could affect the prothrombin time - international normalized ratio (PT-INR). The patients who use drugs like antibiotics have an elevated risk of experiencing an expansion of hemorrhage during extractions from the teeth procedures, so dentists need to be on the lookout for and regularly observe the patients' INR levels.[25] Nearly 70% of people with dental difficulties report using herbs, including ginseng, garlic, ginkgo biloba, echinacea, and St. John's wort, before undergoing a dental procedure, which has been linked to an increased risk of clot formation. Concerning the entire natural medicine is expected to end at the very least one week in advance.[26]
Managing Bleeding Risk in Dental Procedures:
For situations with significant hemorrhage or infection-induced tissue growth, referrals for specialized oral and maxillofacial surgical centers are essential. Hospitalized individuals taking blood thinners should have their bleeding halted before they are discharged. Packing or suturing must be conducted with attention. Oral blood thinners are often not recommended to be stopped during any procedure; rather, they ought to be delayed. Since they enhance the likelihood of bleeding problems, medicines that include aspirin, ibuprofen, or diclofenac should be used carefully.[27] Although there has been no indication of extensive hemorrhaging in patients not on blood-thinning medications, people on aspirin regimens are not entitled to a purposeful intervention in blood-thinning medicines. For individuals on blood-thinning medications, it is best to think about a different treatment plan before the planned day or week in case of a bleeding occurrence. This will give the bleeding enough time to cease.
Factors of Thrombosis in Patients When Discontinuing Anticoagulation Therapy:
Recent research has questioned the regular cessation of oral anticoagulant medication for dental procedures. Stopping anticoagulant treatment and a condition called a “rebound phenomenon,” which causes a rapid rise in the coagulation process or stimulation of platelets when medical treatment is abruptly stopped, both exacerbatethis potential danger.[28]
It must be remembered that eliminating anticoagulant medication can have major repercussions, including harming heart valve replacement devices and possibly creating lethal clotting episodes among patients with dental conditions. Anticoagulant therapy disruption has been associated with a rising likelihood of bleeding-related problems enduring any dental management, such as single or multiple tooth extractions or periodontal surgical treatments.[29]
Factors of complications in patients with prolonged anticoagulant medication:
Advanced age renal disorders and anemia elevate bleeding potential. INR is imperative for assessing hemorrhage chances, alongside levels above 3.0 linked to increased bleeding chances (target range: 2.0-3.0). Some studies suggest tooth extractions can be safely done without stopping anticoagulants. Measuring INR before dental treatment helps prevent blood loss. Adverse effects oforal anticoagulants canraise the chance of hemorrhage and patients should follow anticoagulant clinic guidelines for postoperative pain management. Paracetamol is recommended for short-term mild to moderate pain relief in warfarin users. The risk of hemorrhage doubles when NOACS are combined with NSAIDs, while COX-2 inhibitors may have less impact on bleeding, though conclusive human studies are lacking.[30]
Management of Patients on Warfarin or Vitamin K Therapy:
The British National Formulary recommends that for 2months, a stable patient must maintain their INR readings below 4. The best course of action in treating individuals receiving warfarin is to avoid changing their vitamin K antagonist drugs. This figure ought to be below 4INR.[31] In certain studies, various important questions come up during regular dental practice regarding managing warfarin therapy during dental treatments. However, this presents a challenging situation for clinical practitioners due to inadequate data, leading to uncertainty for practitioners.[32]
Management of patients under a novel oral anticoagulant (NOAC):
Since it additionally inhibits thrombin (FactorIIa) or Factor Xa, respectively, they typically do not need to be routinely monitored in a lab; despite considerable variation across reagents, the prothrombin time is unresponsive to dabigatran at 100 ng mL and frequently stays within the typical range.[33] Despite being considerably more susceptible to rivaroxaban, the prothrombin time still varies significantly among agents. PT can help assess anticoagulation levels among individuals with rivaroxaban, but it is unable to determine precise dosage levels. It has a shorter half-life than warfarin and acts more swiftly (2-4 hours).[34]Although there is no data to support stopping or continuing NOACs during dental surgeries, the risk of thrombosis is usually minimal with a brief interruption. Nevertheless, the likelihood of clotting varies according to the procedure's type and the health of the individual.[35]
Management of patients who are under injectable anticoagulants:
LMWHssuch as Lovenox, Fragmin, and Innohep are frequently used to treat a variety of heart disease disorders and are advantageous for pregnant women and those with cancer-related venous thrombosis, in contrast to heparin-based anticoagulants. LMWHS are taken once or twice a day and their effects peak two to four hours after ingestion. Their half-life is three to five hours compared to other anticoagulants like warfarin. They provide more stability and predictability, which lessens the need for routine monitoring to guarantee safe and efficient management. Further clinical data about the dental treatment of patients utilizing LMWHS is necessary.[36]
Management of some drug interactions prescribed in dental treatment:
Numerous drug interactions have been recorded involving anticoagulant medications like warfarin or acenocoumarol and various antibiotics, including macrolides, erythromycin, clarithromycin, azithromycin, or sulphonamides, which cause a high risk of hemorrhage. Patients should contact their healthcare provider for INR testing and dosage review if bleeding risks are high. Anecdotal reports suggest that amoxicillin can interact with warfarin to elevate prothrombin time. Such occurrences are rare, and monitoring is essential, mostly with antibiotics like metronidazole, where dosage adjustments of warfarin may be required. Because they interfere with the production of vitamin K during coagulation treatment, medications such as levofloxacin, doxycycline, and extended-spectrum cephalosporins can exacerbate hypoprothrombinaemia. Even if there are fewer interactions between dabigatran and rivaroxaban, older patients who receive DOACS are still more likely to hemorrhage because of potential drug-drug interactions.[37] Clindamycin should only be recommended by specialists since it may decrease the production of vitamin K. Coadministration of systemic azole antifungals with HIV medication is typically not advised for patients on rivaroxaban, while fluconazole may have a less significant impact. Furthermore, rivaroxaban and NSAIDs can greatly lengthen bleeding duration without influencing platelet accumulation.[38]
CONCLUSION
In conclusion, stopping anticoagulant medication for dental operations increases the risk of an unnecessary embolism, although post-procedural bleeding is usually controllable with the right treatment for patients taking anticoagulants like dabigatran, rivaroxaban, or apixaban. It is important to consult their doctor before undergoing any dental procedures because the interaction of other medications such as antibiotics antifungals NSAIDS and platelet aggregation inhibitors can further affect bleeding control warfarin user therapeutic INR levels are maintained and their unique risks of bleeding and clotting are carefully controlled when dentists and doctors communicate well, in the end, a customized strategy that combines dental and medical knowledge is essential to attaining safe and successful patient outcomes.
Ethical approval:
Institutional Review Board approval is not required.
Declaration of patient consent:
Patient’s consent is not required as there are no patients in this study.
Conflicts of interest:
There are no conflicts of interest.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation:
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript, and no images were manipulated using AI.
Financial support and sponsorship: Nil
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