Which Factors Determine the Success of Anticoagulation with Warfarin

authors:

avatar Akif Bayyigit ORCID 1 , * , avatar Mustafa Genco Erdem ORCID 2 , avatar Erdal Belen 3 , avatar Mehmet Kucuk ORCID 1

Department of Internal Medicine, Prof. Dr. Cemil Tascioglu City Hospital, Istanbul, Turkey
Department of Internal Medicine, Beykent University, Istanbul, Turkey
Department of Cardiology, Sultangazi Haseki Training and Research Hospital, Istanbul, Turkey

how to cite: Bayyigit A, Erdem M G, Belen E, Kucuk M. Which Factors Determine the Success of Anticoagulation with Warfarin. Int J Cardiovasc Pract. 2023;8(1):e140879. https://doi.org/10.5812/intjcardiovascpract-140879.

Abstract

Background:

Warfarin is a drug most commonly used for anticoagulation. Its efficiency depends on remaining in the demanded therapeutic range.

Objectives:

In this study, the relation between the time in therapeutic range (TTR) and sociodemographic characteristics, comorbidities, and drugs used was investigated for the patient’s use of warfarin.

Methods:

Among patients admitted to the Internal Diseases Polyclinic or taking inpatient treatment in internal diseases service, 50 female and 50 male patients using warfarin were selected starting from the closest date based on their admittance dates. Using patient files and hospital automation system data, TTR levels were calculated with the Rosendaal method, and sociodemographic characteristics, comorbidities, and drugs used were recorded. Patients were separated into 2 groups, TTR > 60% and TTR < 60%, and relations between sociodemographic characteristics, comorbidities, and drugs used were investigated among these groups.

Results:

Time in therapeutic range was found to be over 60% in 34% of the patients. It was observed that gender, occupation and education level, body mass index, smoking ratios, comorbid diseases, drugs used, serum creatinine, and alanine aminotransferase (ALT) levels were similar among TTR groups. The use of drugs lowering the warfarin effect was found to be similar among TTR groups.

Conclusions:

It was observed that sociodemographic characteristics, comorbid diseases, used drugs, serum creatinine, and ALT levels of the patients didn't affect the time in the therapeutic range.

1. Background

Warfarin is a pharmacological agent used for sixty years in the treatment and prevention of venous and arterial thromboembolic events. It was used as the only oral anticoagulant until novel oral anticoagulants (NOAC) were discovered (1). Although it has advantages such as daily single dose use, oral intake easiness, and low price, it also has disadvantages such as narrow therapeutic range, high drug-drug interaction, and high drug-nutrient interaction (2).

Warfarin is used for the treatment of diseases such as pulmonary thromboembolism (PTE), deep vein thromboembolism (DVT), and atrial fibrillation-related (AF) cerebrovascular event prevention, which may cause severe mortality and morbidity (3). To be effective, it should be present at a certain level in the blood. Thromboembolic protection cannot be provided below this level, and it may cause fatal bleeding when it is above this level. Thus, keeping warfarin within the therapeutic range is very important to prevent thromboembolic events, which is the primary objective, and to prevent undesired effects (2).

"International normalized ratio" (INR) is used to measure the therapeutic levels of warfarin. Keeping INR within the therapeutic range detected based on the disease is important for preventing mortality and morbidity. Thus, it is important to calculate the time in the therapeutic range desired during the period of use for patients using warfarin. To achieve this, time in therapeutic range (TTR) must be calculated for every patient. Time in the therapeutic range shows us the percentage of the time during which a patient uses warfarin within the therapeutic range (2, 4, 5).

For effective warfarin treatment, the TTR level should be 60% and above (2). High drug-drug interaction, drug-nutrient interaction of warfarin, and requirement of regular INR control are difficulties requiring the patient to understand the importance of treatment and increasing the need for patient and treatment compliance. The prescribing doctor should make it suitable for the patient due to treatment difficulties such as patient comorbidities and chronic drugs used.

2. Objectives

The objective of this study was to investigate the relationship between TTR levels and sociodemographic characteristics of patients using warfarin and the drugs they used and to investigate factors that can assist in the achievement of optimal TTR levels.

3. Methods

This study was considered ethically appropriate based on Sağlık Bilimleri University (S.B.U.) Okmeydanı Training and Research Hospital Ethics Board decree no 450. Files of patients who were admitted to S.B.U. Okmeydanı Training and Research Hospital Internal Diseases Polyclinics and used warfarin were scanned retrospectively. Patients who were using therapeutic warfarin and had a minimum INR level of 2 under the warfarin effect were included in the study. Patients who were under 18 years of age and those who used warfarin for purposes other than treatment (such as suicide) were not included in the study. Files were scanned both in the physical environment and through the hospital automation system. Among patients admitted for INR control between 06.04.2014 and 06.04.2016 who met the inclusion criteria, 50 male and 50 female patients, starting from those whose admission date for control was on the nearest, were included in the study. Exclusion criteria were determined as patient age under 18 or warfarin use for causes other than treatment (such as suicide). An equal number of female and male patients was included to investigate the effect of gender on TTR.

Information about age, gender, education level, occupation, weight, height, smoking and alcohol use, chronic diseases, drugs used, warfarin starting date, warfarin usage indication, INR, creatinine and alanine aminotransferase (ALT) levels were recorded for all study subjects.

The information was inputted into the Microsoft Excel 2013 software. Body mass index (BMI) was calculated by dividing weight in kilograms by the square of height in meters. Time in therapeutic range was calculated using the Rosendaal method.

3.1. Statistical Method

Mean, standard deviation, median minimum, maximum, frequency, and ratio values were used in definitive data statistics. Kolmogorov Smirnov test was used to measure the distribution of the variables. Mann-Whitney U test and independent sampling t-test were used to analyze the quantitative data. The chi-square test was used for qualitative data analysis, and the Fisher test was used when chi-square test conditions were not met. The Kappa compliance test was used for compliance analysis. SPSS 22.0 program was used for the analyses.

4. Results

Mean age was calculated as 61.7 ± 13.2 (24 - 89) years. Average body weight (kg) was detected as 82.5 ± 16.9 (50 - 130), average height (cm) was 166.4 ± 9.5 (150 - 188), and average BMI was 29.8 ± 5.7 (19 - 45). It was observed that TTR levels were 60% and above for 34 patients and over 60% for 66 patients (Table 1).

Table 1.

Sociodemographic Characteristics and Time in Therapeutic Range levels

Min - MaxMedianMean ± SD or No. (%)
Age24 - 896261.7 ± 13.2
Gender
Woman50 (50.0)
Male50 (50.0)
Weight (kg)50 - 1308082.5 ± 16.9
Length (cm)150 - 188165166.4 ± 9.5
BMI 19 - 452929.8 ± 5.7
Cigarette use 17 (17.0)
Alcohol use5 (5.0)
Profession0.0
Unemployed-housewife36 (36.0)
Retired39 (39.0)
Worker11 (11.0)
Officer4 (4.0)
Self-employment10 (10.0)
Education status 0.0
Illiterate20 (20.0)
Literate 21 (21.0)
Primary school41 (41.0)
Middle school 3 (3.0)
High school13 (13.0)
University2 (2.0)
TTR % Rosendaal0 - 1004947.7 ± 28.9
TTR Rosendaal
< 6066 (66.0)
> 6034 (34.0)
TTR %0 - 1003840.9 ± 24.4
TTR
< 6070 (70.0)
> 6030 (30.0)

The average age was detected as 62.9 ± 13.5 for the group with TTR below 60% and as 59.4 ± 12.5 for the group with TTR of 60% and above. Thirty-four of those with TTR below 60% were female (51.5%), and 32 were male (48.5%); 16 of those with TTR of 60% and above were female (47.1%), and 18 were male (52.9%). Based on the BMI of the patients, 30 ± 5.3 was the average for the group with TTR < 60%, and 29.4 ± 6.5 was the average for the group with TTR > 60%. Eleven patients were smokers (16.7%), and 3 patients drank alcohol (4.5%) in the group with TTR < 60%; 6 patients were smokers (17.6%), and 2 patients drank alcohol (5.9%) in the group with TTR > 60%. The 2 groups had similar occupations and education levels (Table 2).

Table 2.

Relation Between Sociodemographic Characteristics and Time in Therapeutic Range Groups

TTR Rosendaal < 60TTR Rosendaal > 60P
Mean ± SD or No. (%)MedianMean ± SD or No. (%)Median
Age62.9 ± 13.562.559.4 ± 12.561.50.209
Gender 0.673
Female34 (51.5)16 (47.1)
Male32 (48.5)18 (52.9)
Weight (kg)82.9 ± 16.583.081.6 ± 17.880.00.597
Length (cm)166.1 ± 8.9164.0167.0 ± 10.7166.50.875
BMI 30.0 ± 5.329.029.4 ± 6.528.70.449
Cigarette use11 (16.7)6 (17.6)0.902
Alcohol use3 (4.5)2 (5.9)1.000
Profession0.916
Unemployed-housewife24 (36.4)12 (35.3)
Retired25 (37.9)14 (41.2)
Worker8 (12.1)3 (8.8)
Officer1 (1.5)3 (8.8)
Self-employment8 (12.1)2 (5.9)
Education status 0.629
Illiterate15 (22.7)5 (14.7)
Literate14 (21.2)7 (20.6)
Primary school26 (39.4)15 (44.1)
Middle school3 (4.5)0 (0.0)
High school8 (12.1)6 (17.6)
University1 (1.5)1 (2.9)
TTR % Rosendaal31.0 ± 18.831.980.1 ± 12.878.9
TTR %28.9 ± 17.731.064.2 ± 18.160.50.000
TTR0.000
< 6066 (100.0)4 (11.8)
> 600 (0.0)30 (88.2)
Creatinine1.0 ± 0.30.91.2 ± 0.80.950.820
ALT19.7 ± 10.51718.9 ± 12.2160.360

Comorbid disease, chronic drug use, and drug use interacting with warfarin were similar among the groups (Table 3).

Table 3.

Relation Between Comorbid Diseases, Drugs Used, and Warfarin Use Indications and Time in Therapeutic Range Groups

No. (%)P
TTR Rosendaal < 60TTR Rosendaal > 60
Comorbid disease
DM 15 (22.7)7 (20.6)0.807
IHD 46 (69.7)25 (73.5)0.689
HF 45 (68.2)21 (61.8)0.521
HT 31 (47.0)17 (50.0)0.774
HL 11 (16.7)7 (20.6)0.629
CKD 6 (9.1)2 (5.9)0.575
COPD 9 (13.6)2 (5.9)0.240
Thyroid disease6 (9.1)6 (17.6)0.212
BPH 4 (6.1)5 (14.7)0.152
Medication use
OAD 10 (15.2)7 (20.6)0.493
Insulin6 (9.1)1 (2.9)0.254
Anti HT36 (54.5)19 (55.9)0.899
Anti lipid11 (16.7)7 (20.6)0.629
Anti arrhythmic57 (86.4)29 (85.3)0.884
Antiplatelet15 (22.7)7 (20.6)0.807
PPI30 (45.5)13 (38.2)0.490
SSRI11 (16.7)4 (11.8)0.515
Thyroid medication6 (9.1)6 (17.6)0.212
Diuretics40 (60.6)22 (64.7)0.689
Indication for the use of warfarin
AF43 (65.2)27 (79.4)
Metallic valve replacement20 (30.3)5 (14.7)
DVT3 (4.5)1 (2.9)
Pulmonary embolism 0 (0.0)1 (2.9)
Medicines to reduce the effect of warfarin 29 (43.9)14 (41.2)0.791

5. Discussion

Time in the therapeutic range was found in over 60% of 34% of the patients. It was observed that gender, occupation and education level, body mass index, smoking status, comorbid diseases, drugs used, serum creatinine, and ALT levels were similar among TTR groups. The use of drugs decreasing the warfarin effect was found to be similar among TTR groups.

Although the number of patients using DOACs has surpassed warfarin in recent years, many patients are still on warfarin (6). As diseases such as AF, DVT, and PTE requiring anticoagulant use increase with increasing life expectancy, oral anticoagulant usage has also increased. Atrial fibrillation-related is the most common chronic cardiac rhythm disorder (7). While the prevalence of AF is 1/100 in the general population, this rate increases to 1/10 in the elderly (8). Ischemic stroke is the major complication caused by AF (9). Warfarin is used for protection against thromboembolic events such as ischemic stroke caused by AF. DVT and PTE are cardiovascular events that have the third highest prevalence after acute coronary syndrome and stroke, and they have the third highest prevalence among hospital-caused deaths (10, 11). Although warfarin is used for the treatment of diseases with high mortality and morbidity, its dosing adjustment is challenging due to its narrow therapeutic range, high drug-drug and drug-nutrient interactions, and the requirement of regular INR control. Wrong use of warfarin treatment can lead to complications with high mortality and morbidity, such as hemorrhagic stroke and gastrointestinal bleeding (12, 13). Therefore, maintaining warfarin dose within the required therapeutic range has vital importance.

In this study, the TTR level of only 34% of the patients was found to be equal to or higher than 60%, which is the warfarin treatment benefit threshold. In post-hoc analyses made by Connolly et al. with ACTIVE W study data, important differences were found in TTR levels among the countries and centers (14). In the study conducted by Pokorney et al. using data from the ORBIT-AF study, it was similarly demonstrated that TTR levels were different among the centers, and centers with anticoagulation clinics had higher TTR levels (15). It can be claimed that the low number of patients within the therapeutic range in this study could be due to the lack of a separate anticoagulation clinic in the hospital where the study was conducted and the irregular follow-ups as the polyclinic appointments were given from the central hospital appointment system.

The average age of the patients participating in the study was 61.7 ± 13.2 years. As life expectancy increases and the elderly population expands, diseases that need anticoagulants increase and turn into an important health problem. No statistically significant difference was found when we compared the ages of patients with and without TTR levels of 60% and above. In studies made by Pokorney et al. and Ciurus et al., patients were grouped based on a certain TTR level, and, similar to this study, the relationship with age was investigated, and it was observed that age had no effect in this regard (15, 16). In studies conducted by Wieloch et al. and Dlott et al., a positive correlation was found between age and TTR levels. Still, this difference may be due to the fact that the patients were compared on a numeric basis, and they were not separated into 2 groups based on TTR levels (17, 18). In light of this data, it is observed that age affects TTR levels, but the effect of age was not observed when patients below and above a certain TTR level were compared. When we compared the effect of education and occupation of patients with and without TTR levels below 60%, no statistically significant differences were observed with regard to these conditions. In the study by Pokorney et al., it was observed that college graduates had higher TTR percentages. This inconsistency with the current study may be due to the lack of a statistical difference, as only 2% of the patients were university graduates (15).

In the study, Apostolakis et al. developed SAMe-TT2R2 scoring with the outcomes; it was demonstrated that the female gender had a negative effect on TTR level (19). The negative effect of the female gender on anticoagulation control was confirmed in the studies by Lobos-Bejarano et al. and Rose et al. (20, 21). Similar to the findings of Pokorney et al. and Celik et al., it was demonstrated that gender did not have any influence on TTR levels in this study (15, 22). Therefore, it seems that further studies with larger samples are necessary to determine the gender effect. Smoking increases warfarin clearance by inducing cytochrome enzymes (23), and the INR level of smokers should be checked more often. The strong negative connection between smoking and TTR level was demonstrated in the Apostolakis et al. (19) study, and smoking had a score of 2 in SAMe-TT2R2 scoring. Similar to this study, in studies by Chan et al. (24) and McGriff-Lee et al. (25), a statistically significant connection was not observed between smoking and TTR levels (24, 25). Although many studies have confirmed that SAMe-TT2R2 scoring can predict non-conforming TTR levels with a high probability, the effect of only smoking is unclear when these results are considered.

Patients using warfarin are generally elderly patients with many comorbidities and regular drug use. Thus, the relationship between TTR level and comorbidity and drug use is very important and was one of the main objectives of this study. No statistically significant relationship was observed between comorbid diseases and drug use and TTR levels. No relationship was shown between comorbidities and TTR level in the Wypasek et al. study (26). A negative correlation with arterial hypertension in the study by Ciurus et al. was demonstrated, but no relationship was observed with other comorbidities (16). A negative correlation was also shown with anemia, chronic obstructive pulmonary disease (COPD), diabetes mellitus (DM), chronic kidney disease (CKD), and CHF in the study by Pokorney et al. (15). Similar to this study, in the study by Apostolakis et al., it was demonstrated that individual comorbidities did not affect TTR levels. However, when 2 or more comorbidities coexist, they have a negative correlation with TTR levels (19). However, similar to our study, all other important studies compared the patients by separating them into 2 - 4 groups based on their TTR levels. The TTR values of the patients with a therapeutic level below the demanded value (ex: TTR > 60%) do not have numeric importance because these patients do not benefit from the warfarin treatment regardless of their TTR levels. Warfarin may even have a negative effect as it increases the risk of bleeding (27, 28). When this situation is considered, data acquired from this study can be of more clinical importance.

Drug-drug interactions are another warfarin treatment challenge that should be considered and may be difficult to manage for both patients and physicians. In addition to documented drug interactions (Table 2), many interactions are published in the literature as case reports. Although many studies have investigated the effects of drugs on warfarin dose and INR level, there are very few studies investigating this relationship with TTR. When TTR levels of patients using drugs that lower warfarin’s effect was checked, no statistically significant difference was seen between the 2 groups. Similar to this study, in the study by McGriff-Lee et al., it was demonstrated that there was no statistically significant relationship between TTR levels and the use of drugs influencing warfarin levels (25). These results can be interpreted as a statistically significant issue due to the low number of studies and the inadequate number of patients and also due to the fact that follow-ups were managed based on using interacting drugs use by both the patient and the doctor provided INR stability and were not effective on TTR. Current guidelines on anticoagulation recommend that patients using interacting drugs or those with a new drug added to their treatment should be followed up more stringently (2, 3).

The study's limitations include being single-centered, having a small number of patients, and being retrospective.

5.1. Conclusions

In conclusion, this study demonstrated that no single factor is effective on the TTR level, and many factors affect the TTR level cumulatively. Although scoring systems are available, there is no adequate data to predict TTR lability. Following patients regularly in the light based on updated guidelines and urgently adjusting treatment in patients with labile INR appears rational to keep TTR within the desired range.

References

  • 1.

    Cecil RL, Goldman L, Schafer AI. Goldman's Cecil medicine. Philadelphia: Saunders; 2012.

  • 2.

    Ageno W, Gallus AS, Wittkowsky A, Crowther M, Hylek EM, Palareti G. Oral anticoagulant therapy: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines. Chest. 2012;141(2 Suppl):e44S-88. [PubMed ID: 22315269]. [PubMed Central ID: PMC3278051]. https://doi.org/10.1378/chest.11-2292.

  • 3.

    Holbrook A, Schulman S, Witt DM, Vandvik PO, Fish J, Kovacs MJ, et al. Evidence-based management of anticoagulant therapy: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines. Chest. 2012;141(2 Suppl):e152S-84. [PubMed ID: 22315259]. [PubMed Central ID: PMC3278055]. https://doi.org/10.1378/chest.11-2295.

  • 4.

    Schmitt L, Speckman J, Ansell J. Quality assessment of anticoagulation dose management: comparative evaluation of measures of time-in-therapeutic range. J Thromb Thrombolysis. 2003;15(3):213-6. [PubMed ID: 14739631]. https://doi.org/10.1023/B:THRO.0000011377.78585.63.

  • 5.

    Rosendaal FR, Cannegieter SC, van der Meer FJ, Briet E. A method to determine the optimal intensity of oral anticoagulant therapy. Thromb Haemost. 1993;69(3):236-9. [PubMed ID: 8470047].

  • 6.

    Navar AM, Kolkailah AA, Overton R, Shah NP, Rousseau JF, Flaker GC, et al. Trends in Oral Anticoagulant Use Among 436 864 Patients With Atrial Fibrillation in Community Practice, 2011 to 2020. J Am Heart Assoc. 2022;11(22):e026723. [PubMed ID: 36346063]. [PubMed Central ID: PMC9750070]. https://doi.org/10.1161/JAHA.122.026723.

  • 7.

    Ezekowitz MD. Atrial fibrillation: the epidemic of the new millennium. Ann Intern Med. 1999;131(7):537-8. [PubMed ID: 10507965]. https://doi.org/10.7326/0003-4819-131-7-199910050-00011.

  • 8.

    Stewart S, Murphy NF, Walker A, McGuire A, McMurray JJ. Cost of an emerging epidemic: an economic analysis of atrial fibrillation in the UK. Heart. 2004;90(3):286-92. [PubMed ID: 14966048]. [PubMed Central ID: PMC1768125]. https://doi.org/10.1136/hrt.2002.008748.

  • 9.

    Wolf PA, Abbott RD, Kannel WB. Atrial fibrillation as an independent risk factor for stroke: the Framingham Study. Stroke. 1991;22(8):983-8. [PubMed ID: 1866765]. https://doi.org/10.1161/01.str.22.8.983.

  • 10.

    Goldhaber SZ. Pulmonary embolism thrombolysis: a clarion call for international collaboration. J Am Coll Cardiol. 1992;19(2):246-7. [PubMed ID: 1732348]. https://doi.org/10.1016/0735-1097(92)90473-z.

  • 11.

    Oktay E. Will NOACs become the new standard of care in anticoagulation therapy? Int J Cardiovasc Acad. 2015;1(1):1-4. https://doi.org/10.1016/j.ijcac.2015.06.007.

  • 12.

    Pisters R, Lane DA, Nieuwlaat R, de Vos CB, Crijns HJ, Lip GY. A novel user-friendly score (HAS-BLED) to assess 1-year risk of major bleeding in patients with atrial fibrillation: the Euro Heart Survey. Chest. 2010;138(5):1093-100. [PubMed ID: 20299623]. https://doi.org/10.1378/chest.10-0134.

  • 13.

    Hylek EM, Singer DE. Risk factors for intracranial hemorrhage in outpatients taking warfarin. Ann Intern Med. 1994;120(11):897-902. [PubMed ID: 8172435]. https://doi.org/10.7326/0003-4819-120-11-199406010-00001.

  • 14.

    Connolly SJ, Pogue J, Eikelboom J, Flaker G, Commerford P, Franzosi MG, et al. Benefit of oral anticoagulant over antiplatelet therapy in atrial fibrillation depends on the quality of international normalized ratio control achieved by centers and countries as measured by time in therapeutic range. Circulation. 2008;118(20):2029-37. [PubMed ID: 18955670]. https://doi.org/10.1161/CIRCULATIONAHA.107.750000.

  • 15.

    Pokorney SD, Simon DN, Thomas L, Fonarow GC, Kowey PR, Chang P, et al. Patients' time in therapeutic range on warfarin among US patients with atrial fibrillation: Results from ORBIT-AF registry. Am Heart J. 2015;170(1):141-8-e1. [PubMed ID: 26093875]. https://doi.org/10.1016/j.ahj.2015.03.017.

  • 16.

    Ciurus T, Cichocka-Radwan A, Lelonek M. Factors affecting the quality of anticoagulation with warfarin: experience of one cardiac centre. Kardiochir Torakochirurgia Pol. 2015;12(4):334-40. [PubMed ID: 26855650]. [PubMed Central ID: PMC4735535]. https://doi.org/10.5114/kitp.2015.56784.

  • 17.

    Wieloch M, Sjalander A, Frykman V, Rosenqvist M, Eriksson N, Svensson PJ. Anticoagulation control in Sweden: reports of time in therapeutic range, major bleeding, and thrombo-embolic complications from the national quality registry AuriculA. Eur Heart J. 2011;32(18):2282-9. [PubMed ID: 21616951]. https://doi.org/10.1093/eurheartj/ehr134.

  • 18.

    Dlott JS, George RA, Huang X, Odeh M, Kaufman HW, Ansell J, et al. National assessment of warfarin anticoagulation therapy for stroke prevention in atrial fibrillation. Circulation. 2014;129(13):1407-14. [PubMed ID: 24493817]. https://doi.org/10.1161/CIRCULATIONAHA.113.002601.

  • 19.

    Apostolakis S, Sullivan RM, Olshansky B, Lip GYH. Factors affecting quality of anticoagulation control among patients with atrial fibrillation on warfarin: the SAMe-TT2R2 score. Chest. 2013;144(5):1555-63. [PubMed ID: 23669885]. https://doi.org/10.1378/chest.13-0054.

  • 20.

    Lobos-Bejarano JM, Barrios V, Polo-Garcia J, Escobar C, Vargas-Ortega D, Marin-Montanes N, et al. Evaluation of SAMe-TT2R2 score and other clinical factors influencing the quality of anticoagulation therapy in non-valvular atrial fibrillation: a nationwide study in Spain. Curr Med Res Opin. 2016;32(7):1201-7. [PubMed ID: 26967541]. https://doi.org/10.1185/03007995.2016.1164676.

  • 21.

    Rose AJ, Hylek EM, Ozonoff A, Ash AS, Reisman JI, Berlowitz DR. Risk-adjusted percent time in therapeutic range as a quality indicator for outpatient oral anticoagulation: results of the Veterans Affairs Study to Improve Anticoagulation (VARIA). Circ Cardiovasc Qual Outcomes. 2011;4(1):22-9. [PubMed ID: 21098779]. https://doi.org/10.1161/CIRCOUTCOMES.110.957738.

  • 22.

    Celik A, Izci S, Kobat MA, Ates AH, Cakmak A, Cakilli Y, et al. The awareness, efficacy, safety, and time in therapeutic range of warfarin in the Turkish population: warfarin -tr. Anatol J Cardiol. 2015;16(8):595-600. https://doi.org/10.5152/AnatolJCardiol.2015.6474.

  • 23.

    Nathisuwan S, Dilokthornsakul P, Chaiyakunapruk N, Morarai T, Yodting T, Piriyachananusorn N. Assessing evidence of interaction between smoking and warfarin: a systematic review and meta-analysis. Chest. 2011;139(5):1130-9. [PubMed ID: 21540214]. https://doi.org/10.1378/chest.10-0777.

  • 24.

    Chan PH, Li WH, Hai JJ, Chan KH, Tse HF, Cheung BM, et al. Gastrointestinal haemorrhage in atrial fibrillation patients: impact of quality of anticoagulation control. Eur Heart J Cardiovasc Pharmacother. 2015;1(4):265-72. [PubMed ID: 27532451]. https://doi.org/10.1093/ehjcvp/pvv032.

  • 25.

    McGriff-Lee NJ, Csako G, Chen JT, Dang DK, Rosenfeld KG, Cannon RO, et al. Search for predictors of nontherapeutic INR results with warfarin therapy. Ann Pharmacother. 2005;39(12):1996-2002. [PubMed ID: 16288081]. https://doi.org/10.1345/aph.1E381.

  • 26.

    Wypasek E, Mazur P, Bochenek M, Awsiuk M, Grudzien G, Plicner A, et al. Factors influencing quality of anticoagulation control and warfarin dosage in patients after aortic valve replacement within the 3 months of follow up. J Physiol Pharmacol. 2016;67(3):385-93. [PubMed ID: 27511999].

  • 27.

    Morgan CL, McEwan P, Tukiendorf A, Robinson PA, Clemens A, Plumb JM. Warfarin treatment in patients with atrial fibrillation: observing outcomes associated with varying levels of INR control. Thromb Res. 2009;124(1):37-41. [PubMed ID: 19062079]. https://doi.org/10.1016/j.thromres.2008.09.016.

  • 28.

    Wan Y, Heneghan C, Perera R, Roberts N, Hollowell J, Glasziou P, et al. Anticoagulation control and prediction of adverse events in patients with atrial fibrillation: a systematic review. Circ Cardiovasc Qual Outcomes. 2008;1(2):84-91. [PubMed ID: 20031794]. https://doi.org/10.1161/CIRCOUTCOMES.108.796185.