Cor Vasa 2019, 61(3):e266-e271 | DOI: 10.33678/cor.2019.023
Potential drug-drug interactions between oral anticoagulants for high-risk patients with atrial fibrillation in Latvia
- a Riga Stradins University, Faculty of Medicine, Latvia
- b Riga Stradins University, Division of Doctoral Studies, Latvia
- c Riga Stradins University, Department of Internal Diseases, Latvia
Introduction: Atrial fibrillation (AFib) is a disease that affects many people, especially elderly ones. All of these persons have an increased risk of thromboembolic event. For lowering the risk these patients use anticoagulation therapy. There are two types of oral anticoagulants - vitamin K antagonist warfarin and new, known also as direct oral anticoagulants, dabigatran and rivaroxaban. Due to several comorbidities and other complications, e.g. the risk of bleeding and thromboembolism, AFib patients are using different medication simultaneously, therefore increasing the risk of drug-drug interactions because of one metabolism path through P-glycoprotein and CYP450. Monitoring of medical therapy and patient education about most frequent drug-drug interactions using oral anticoagulants could raise attention of health care professionals to the possible drug-drug interactions and promote safe and effective anticoagulation therapy., Aim: To define and analyze the most common potential drug-drug interactions for most frequent used oral anticoagulants - warfarin, dabigatran, rivaroxaban - in patients with high-risk AFib in Latvia., Materials and methods: Quantitative analytic cross-section research was made in time period from October 2016 till June 2017 in Pauls Stradins clinical university hospital, Center of Cardiology in Latvia. The data about patients with high-risk AFib who used oral anticoagulants daily were selected. After signed patients consent form the demographic data, regularly and frequently used medication and food supplements were obtained. Laboratory analysis and echocardiography data were specified with the help of case anamnesis. For statistical data analysis were used SPSS Statistics database., Results: Altogether 143 patients were enrolled in this study, from which 46.2% were male, 53.8% female, with the mean age 69.7 (SD 9.9) years. 53.8% used warfarin, 16.1% dabigatran and 33.6% used rivaroxaban. 49.7% of patients had increased risk of possible drug-drug interactions. For warfarin users the most frequent potential interactions were with omega-3 supplements (20.8%), amiodarone (16.7%) and proton pump inhibitors (13.8%). For dabigatran users the most frequent potential interaction was with proton pump inhibitors (26.1%), amiodarone (17.4%) and omega-3 supplements (13.0%). For rivaroxaban users the most frequent potential drug interaction was with amiodarone (29.2%), omega-3 supplements (16.7%) and non-steroidal anti-inflammatory drugs (4.2%)., Conclusion: From all high-risk AFib patients 47.7% had potentially moderate or major risk of drug interactions, most frequently with food supplements. 50.3% patients used warfarin, K vitamin antagonist. The most frequent potential drug interaction in warfarin group was with omega-3 supplements (20.8%) and amiodarone (16.7%), in dabigatran group with proton pump inhibitors (26.1%) and amiodarone (17.4%), in rivaroxaban group with amiodarone (29.2%) and omega-3 supplements (16.7%). Awareness of these interactions between health care professionals could promote the safety and effectiveness of anticoagulation therapy for high-risk atrial fibrillation patients.
Keywords: CYP450 inhibitors, Dabigatran, Monitoring drug use, Patient education, Risk of bleeding
Received: January 9, 2019; Accepted: March 6, 2019; Published: June 21, 2019 Show citation
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References
- Erglis A, Kalvelis A, Kalejs O, Jegere S. Latvijas Kardiologu biedribas 2010. Gada pavasara consensus dokuments Atriju Mirgosanas arstesana. - Riga, 2010. - 5. 6.
- Zoni-Berisso M, Lercari F, Carazza R, Domenicucci S. Epidemiology of atrial fibrillation: European perspective. Clin Epidemiol 2014;6:213-220.
Go to original source...
Go to PubMed...
- Friberg L, Benson L, Rosenqvist M, Lip GY. Assessment of female sex as a risk factor in atrial fibrillation in Sweden: nationwide retrospective cohort study. BMJ 2012;344:e3522.
Go to original source...
Go to PubMed...
- Yang E. A clinician's perspective: novel oral anticoagulants to reduce the risk of stroke in nonvalvular atrial fibrillation - full speed ahead or proceed with caution? Vasc Health Risk Manag 2014;10:507-522.
Go to original source...
Go to PubMed...
- Heidbuchel H, Verhamme P, Alings M, et al. European Heart Rhythm Association Practical Guide on the use of new oral anticoagulants in patients with non-valvular atrial fibrillation. Europace 2013;15:625-
Go to original source...
Go to PubMed...
- Finch A, Pillans P. P-glycoprotein and its role in drug-drug interactions. Aust Prescr 2014;37:137-139.
Go to original source...
- Wessler JD, Grip LT, Mendell J, Giugliano RP. The P-Glycoprotein Transport System and Cardiovascular Drugs. J Am Coll Cardiol 2013;61:2495-2502.
Go to original source...
Go to PubMed...
- Guengerich FP. Cytochrome P450 and Chemical Toxicology. Chem Res Toxicol 2008;21:70-83.
Go to original source...
Go to PubMed...
- Kaminsky LS, Zhang ZY. Human P450 metabolism of warfarin. Pharmacol Ther 1997;73:67-74.
Go to original source...
Go to PubMed...
- Horn JR, Hansen PD. Rivaroxaban: A New Oral Anticoagulant. Pharmacy Times 19 February, 2012. Retrieved July 4, 2017, from http://www.pharmacytimes.com/publications/issue/2012/february2012/rivaroxaban-a-new-oral-anticoagulant
- Urbancika E, Kalnina L, Kalejs O. Statistic review of patients with cardiologic events who are using anticoagulants - total amount of daily used drugs and with those the number of drugs that can interact with anticoagulants. Abstracts from 26th Nordic-Baltic Congress of Cardiology 2017;53(1):12.
- Kirchhof P, Benussi S, Kotecha D, et al. 2016 ESC Guidelines for the management of atrial fibrillation developed in collaboration with EACTS. Eur Heart J 2016;37:2893-2962.
Go to original source...
Go to PubMed...
- Kannan B, Nagella AB, Sathia Prabhu A. et al. Incidence of Potential Drug-Drug Interactions in a Limited and Stereotyped Prescription Setting - Comparison of Two Free Online Pharmacopoeias. Cureus 2016;8:e886.
Go to original source...
Go to PubMed...
- Teixeira JJ, Crozatti MT, dos Santos CA, Romano-Lieber NS. Potential drug-drug interactions in prescriptions to patients over 45 years of age in primary care, southern Brazil. PLoS One 2012;7:e47062.
Go to original source...
Go to PubMed...
- Bucher HC, Achermann R, Stohler N, Meier CR. Surveillance of Physicians Causing Potential Drug-Drug Interactions in Ambulatory Care: A Pilot Study in Switzerland. PLoS One 2016;11:e0147606.
Go to original source...
Go to PubMed...
- Penning-van Beest FJA, Koerselman J, Herings RMC. Quantity and quality of potential drug interactions with coumarin anticoagulants in the Netherlands. Pharmacy World & Science 2007;29;671-675.
Go to original source...
Go to PubMed...
- Bjerrum L, Andersen M, Petersen G, Kragstrup J. Exposure to potential drug interactions in primary health care. Scand J Prim Health Care 2003;21:153-158.
Go to original source...
Go to PubMed...
- El Samia Mohamed SMA, Gad Z, El-Nimr NA, Razek AAHA. Prevalence and Pattern of Potential Drug-Drug Interactions in the Critical Care Units of a Tertiary Hospital in Alexandria, Egypt. ADv. Pharmacoepidemiol Drug Safety 2013;1:144.
- Narum S, Solhaug V, Myhr K, et al Warfarin-associated bleeding events and concomitant use of potentially interacting medicines reported to the Norwegian spontaneous reporting system. Br J Clin Pharmacol 2011;71:254-262.
Go to original source...
Go to PubMed...
- Chamberlain AM, Alonso A, Gersh BJ, et al Multimorbidity and the risk of hospitalization and death in atrial fibrillation: A population-based study. Am Heart J 2017;185:74-84.
Go to original source...
Go to PubMed...
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