Abstract
Purpose: The management of patients with atrial fibrillation (AF) and acute coronary syndrome (ACS) or undergoing percutaneous coronary intervention (PCI) requires appropriate antithrombotic regimens for stroke prevention and in-stent thrombosis. Current practice recommendations are largely based on consensus options as there is limited evidence from randomized clinical trials. Hence, by surveying a group of cardiologists across India, we sought to better understand the current practice patterns of using oral anticoagulants (vitamin K antagonist, VKA or non-vitamin K antagonist oral anticoagulant, NOAC) and antiplatelet therapy in those patients in India.
Methods: A cross-sectional questionnaire-based survey was conducted across India to better understand the clinical practices in AF management.
Results: A total of 151 cardiologists participated in this survey. The most commonly prescribed combination therapy in patients with AF and ACS/undergoing PCI was triple therapy (NOAC + dual antiplatelet [aspirin and P2Y12 inhibitor]) (54.30%) followed by NOAC + single antiplatelet (33.11%). Only 11.26% of cardiologists prescribed VKA + dual antiplatelet therapy. Among anticoagulants, cardiologists prescribed NOACs to 66.11% of patients and VKAs to 25.54% of patients. Among P2Y12 inhibitors, ticagrelor (50.99%) and clopidogrel (47.02%) were the most preferred medication. The physician reported patient adherence rates to NOACs were higher compared to VKAs. Around 41.06% of cardiologists reportedly changed antiplatelet therapy for patients from dual antiplatelet to single antiplatelet therapy in three months; 36.42%, in one month; and 19.21% in six months after PCI. Around 61.59% of cardiologists stopped prescribing antiplatelet therapy for patients by one year.
Conclusion: Our survey demonstrated that the majority of cardiologists used triple therapy (NOAC + dual antiplatelet), followed by NOAC + single antiplatelet for managing patients with AF and ACS or undergoing PCI in line with the available guidelines.
Keywords: vitamin k antagonists, ticagrelor, prasugrel, clopidogrel, aspirin, apixaban
Introduction
Atrial fibrillation (AF) is a global health burden and increases the risk for thromboembolic complications including stroke and other cardiovascular (CV) events [1]. Acute coronary syndrome (ACS) commonly occurs in patients with AF and requires oral anticoagulants (OAC) for the prevention of stroke, in-stent thrombosis, or recurrent cardiac events [2].
Choosing the best anti-thrombotic therapy for these patients is quite challenging as it is difficult to balance thrombosis prevention and the risk of bleeding [3]. Currently, OAC such as vitamin K antagonists (VKAs) and non-VKA OAC (NOAC) are indicated to prevent AF-related ischemic strokes and systemic embolism. However, they are reportedly ineffective in preventing stent thrombosis and are not indicated for secondary prevention after ACS [4-7]. For percutaneous coronary intervention (PCI) or ACS, dual antiplatelet therapy (DAPT) with aspirin and P2Y12 receptor inhibitor (clopidogrel, prasugrel, or ticagrelor) is the gold standard and has proven to reduce the incidence of ischemic events or stent thrombosis but is less effective in reducing cardioembolic stroke [7-10]. To reduce both stroke and ischemic events, triple therapy with OAC and DAPT has been used in the past decade [10]. However, studies have shown that these regimens increase the risk of bleeding [11-13]. Thus, an antithrombotic regimen with an acceptable benefit-risk profile would be valuable in treating patients with AF and associated ACS or PCI.
Several randomized clinical trials have been conducted to evaluate the safety and efficacy of NOACs versus VKA as a combination with single or dual antiplatelet agents in patients with AF and ACS or undergoing PCI [7,14-16]. The RE-DUAL PCI trial demonstrated a lower risk of bleeding among those receiving dual therapy with dabigatran and a P2Y12 inhibitor compared to those receiving triple therapy with warfarin (P2Y12 inhibitor) and aspirin [16]. POINEER AF-PCI trial showed that low-dose rivaroxaban with a DAPT for 6-12 months was associated with low risk of clinically significant bleeding than the therapy with VKA plus DAPT [15].
The AUGUSTUS trial data support use of apixaban (NOAC) and a P2Y12 inhibitor without aspirin during the first six months for most patients owing to an almost twofold increase in bleeding with aspirin use [7]. However, despite the evidence provided by clinical trials and clinical practice guideline recommendations, treatment decisions and the choice and dosage of a particular drug can depend on the patient's clinical profile, cardiologists, and organizational factors [17].
TREAT-RISK, a major global transnational survey of AF treatment patterns reported that appropriate patients with AF are prescribed anticoagulants in the United States (82% of eligible patients on average) and its prescription is the lowest in China (58.1%) [18]. It was observed that minimizing bleeding risk was most important to Indian (7%) and Chinese (7%) healthcare providers [18]. Cardiologists in India (47%) and China (43%) were also least likely to prescribe an anticoagulant for patients over the age of 75 compared to cardiologists in the United Kingdom (92%) and the United States (88%) who were far more likely to frequently anticoagulated patients over age 75 [18].
Hence, by surveying a group of cardiologists across India, we sought to better understand the current practice patterns of using anticoagulants and antiplatelet therapy in an Indian patient with AF and ACS or those undergoing PCI and to identify prescription regimens and physician-reported patient adherence to NOACs and VKAs in clinical practice. These data reveal the current attitude of cardiologists towards prescribing anticoagulants and antiplatelet drugs.
Materials and methods
This study was a cross-sectional questionnaire-based survey of cardiologists across India to better understand the clinical practices in AF management for 6 months in the year 2020. Cardiologists with at least 15 years of experience in the field were invited to participate in the survey. We obtained informed consent from all participating cardiologists before capturing their responses in the survey. The survey focused on the use of OAC and antiplatelets in the Indian patient population with AF and ACS or undergoing PCI. We intended to get insights into the prevailing practice of using an antithrombotic in Indian patients. The questionnaire was validated by ten cardiologists representing different geographies of the country. The questionnaire was characterized by categories on the prevalence of AF, AF, and ACS undergoing PCI and medical treatment, and anticoagulant and antiplatelet usage patterns. The entire survey was conducted using emails, short message service (SMS), and telephonic calls, the survey link was shared with the Cardiologists through email after they have consented to participate in the survey. As the study did not involve the collection or analysis of human data, ethics committee approval was not deemed necessary.
Statistical analyses
Continuous variables were summarized using descriptive statistics including the number of observations, mean, standard deviation (SD), median, and range. Categorical data were summarized as numbers and percentages. Data were summarized/analyzed per the availability of the observed dataset. All statistical analyses were performed using SAS version 9.4 (SAS Institute Inc., Cary, NC, USA).
Since this was a descriptive survey, a former effect size calculation was not required. However, an attempt was made to enroll an adequate number of cardiologists (150) to achieve an appropriate effect size. Since this is a survey about the experiences and preferences of physicians in their practice, and no human clinical data was collected, ethics committee approval was not deemed to be necessary by the authors.
Results
The response rate was (54%, 151/280) in this survey.
Geographical distribution of responses
Upon analyzing the geographical distribution of survey responses (Table 1), the response to the survey was received more from the southern region (48.34%) followed by the northern (19.21%), western (16.56%) and the eastern (5.96%) regions.
Table 1. Prevalence of atrial fibrillation, acute coronary syndrome and its management in routine clinical practice of the cardiologists participating in the survey .
Abbreviations: AF: atrial fibrillation; ACS: acute coronary syndrome; PCI: percutaneous coronary intervention
| Variables | N=151 Median (minimum, maximum)/n (%) |
| Geographical distribution of responses | |
| East | 9 (5.96) |
| West | 25 (16.56) |
| North | 29 (19.21) |
| South | 73 (48.34) |
| Not specified | 15 (9.93) |
| Prevalence of AF in clinical practice | 12 (1, 90) |
| Prevalence of AF & ACS or undergoing PCI in clinical practice | 5 (1, 80) |
| Proportion of patients with ACS undergoing below treatments in clinical practice | |
| Medical management | 20 (0, 90) |
| PCI | 80 (2, 100) |
Prevalence of AF and ACS in clinical practice
A total of 151 cardiologists participated in this survey from different regions across India. The median prevalence of AF, and AF with ACS or those undergoing PCI in clinical practice was reported as 12% and 5%, respectively. Around median of 20% patients with ACS underwent medical management and 80% were reported to undergo PCI (Table 1).
Usage pattern of antiplatelets and anticoagulants
As shown in Figure 1A, cardiologists most commonly selected DAPT comprising aspirin combined with P2Y12 inhibitor (median {min., max.}: 100% {0,100}) followed by P2Y12 inhibitor alone (median {min., max.}: 0% {0, 100}). Aspirin was preferred less often (median {min., max.}: 0 {0, 70}). Among P2Y12 inhibitors (Figure 1B), ticagrelor (50.99%) and clopidogrel (47.02%) were the most preferred medication by cardiologists while prasugrel was the least preferred (1.99%).
Figure 1. (A) Patients (%) with AF and ACS or undergoing PCI who would receive aspirin or P2Y12 inhibitor or dual antiplatelets. (B) Choice of P2Y12 inhibitors among cardiologists.
Abbreviations: AF: atrial fibrillation; ACS: acute coronary syndrome; PCI: percutaneous coronary intervention
Among anticoagulants, NOACs was most commonly prescribed by the cardiologists than VKA (median {min, max}: 80% {0, 100} vs 20% {0, 100}) (Figure 2A). Physician reported patient adherence rates to NOACs was higher compared to VKAs ((median {min, max}: 80% {20, 100}) vs 60% {0,100}) (Figure 2B).
Figure 2. (A) Patients (%) with AF and ACS or undergoing PCI who would be on VKA or NOACs. (B) Patients adherence (>80% of days covered in a year) to warfarin and NOACs in India. (C) Cardiologist (%) changing from dual to single antiplatelet therapy at month 1, 3, and 6. (D) Cardiologist (%) who stop antiplatelet therapy in majority of patients at specific duration.
Abbreviations: AF: atrial fibrillation; ACS: acute coronary syndrome; PCI: percutaneous coronary intervention; VKA: vitamin K antagonists; NOACs: non-vitamin K antagonist oral anticoagulants
The most commonly prescribed combination therapy for managing patients with AF and ACS or those undergoing PCI was triple therapy comprising NOAC combined with dual antiplatelet (54.30%) followed by NOAC with single antiplatelet (33.11%). Only 11.26% of cardiologists prescribed VKA with DAPT (Figure 3A).
Figure 3. (A) Treatment regimen most commonly prescribed for managing patients with AF and ACS or undergoing PCI. (B) Patients (%) who would receive different doses of NOACs.
Abbreviations: AF: atrial fibrillation; ACS: acute coronary syndrome; PCI: percutaneous coronary intervention; VKA: vitamin K antagonists; NOACs: non-vitamin K antagonist oral anticoagulants; OD: once a day; BD: twice a day
Around 41.06% of cardiologists reportedly changed antiplatelet therapy for patients from dual antiplatelet to single antiplatelet therapy in three months; 36.42%, in one month; and 19.21% in six months (Figure 2C). Around 61.59% of cardiologists stopped prescribing antiplatelet therapy for patients by one year and 24.50% stopped after one year (Figure 2D).
Prescribed dose of NOACs in clinical practice
Among NOACs, 5 mg BD (twice daily) dose of apixaban (83.22%), 20 mg OD (once daily) of rivaroxaban (42.28%) and 110 mg BD of dabigatran (51.33%) were the most commonly prescribed doses than other doses (Figure 3B).
Pattern of antiplatelet therapy prescribed with the most commonly prescribed dose of Apixaban
With the most commonly prescribed dose of apixaban (5 mg OD), if we consider the median estimates, P2Y12 inhibitor was prescribed no patients, and DAPT (Aspirin + P2Y12 inhibitor) was prescribed to 100% (0,100) of patients. Ticagrelor (50.0%) and clopidogrel (49.19%) were equally preferred by cardiologists along with apixaban 5 mg OD (Table 2).
Table 2. Pattern of antiplatelet therapy prescribed with the most commonly prescribed dose of Apixaban (5 mg BD).
| Median (minimum, maximum)/n (%) | |
| Proportion of patients who were prescribed only P2Y12 | 0 (0, 100) |
| Proportion of patients who are prescribed dual antiplatelet therapy (Aspirin+P2Y12 inhibitor) | 100 (0, 100) |
| Choice of P2Y12 inhibitor, N (%) | |
| Ticagrelor | 62 (50.0) |
| Clopidogrel | 61 (49.19) |
| Prasugrel | 1 (0.81) |
Discussion
The present survey assessed the pattern of anticoagulant use in patients with AF and ACS or those undergoing PCI. The major findings of this survey reported that the majority of the cardiologists used triple therapy, and predominantly used NOAC + dual antiplatelets (aspirin and P2Y12 inhibitor) followed by NOAC + single antiplatelet for managing patients with AF and ACS or those undergoing PCI. This was in accordance with the recommendations from the current clinical practice guidelines for managing these patients [19]. The VKA + DAPT was prescribed by only 11.26% of cardiologists.
The physician reported patients’ adherence to NOACs was higher compared to VKAs in our survey. Several previous studies reported that the persistence and adherence of patients to NOACs were higher compared to VKAs due to the safety, simplified dosage regimen, and predictable dose-related anticoagulant effect enabling fixed dosing without the need for routine laboratory monitoring [20-22]. The choice for P2Y12 inhibitors was heterogeneous as cardiologists preferred both ticagrelor and clopidogrel however, prasugrel was the least preferred, probably due to the risk associated with bleeding. A recent meta-analysis showed that thrombolysis in myocardial infarction (TIMI) major and minor bleeding events were increased with the usage of prasugrel compared to clopidogrel and ticagrelor in patients with ACS [23]. The NOAC practical guide [24], EHRA consensus [25] and the ESC's DAPT-focused update [26], and the AF guideline [27] discourage using prasugrel or ticagrelor as components of a triple therapy regimen.
In our survey, around 41.06% of cardiologists were reported to change antiplatelet therapy for patients from dual antiplatelet to single antiplatelet therapy in three months, 36.42% in one month, and 19.21% in six months after PCI. Most cardiologists stopped prescribing antiplatelet therapy for patients within one year (61.59%), which is in line with the clinical recommendations based on the clinical scenario characteristics. The AAC/AHA and ESC guidelines recommend using antiplatelet therapy varying from 1 month to an extended duration of more than 12 months depending on the clinical scenario and susceptibility to ischemia, bleeding, or both in patients with AF and ACS or those undergoing PCI [19,26]. A recent North American consensus statement recommends NOACs as the oral anticoagulation of choice, and a dual therapy with NOAC and a P2Y12 inhibitor for six to 12 months is recommended based on the ischemic and bleeding risk of the patients [28].
Among anticoagulants, prescriptions for NOACs were much higher compared to VKAs as recommended in the guidelines [19]. NOACs have multiple pharmacological advantages over VKAs such as rapid onset/offset of action, few food and drug interactions, predictable pharmacokinetics and they do not require regular monitoring for coagulation [29,30]. A meta-analysis of 12 studies on the efficacy and safety of NOACs over warfarin demonstrated that NOACs are superior to the latter in preventing a composite of stroke and systemic embolism in patients with AF [31]. Moreover, NOACs appear to offer advantages over VKAs, by providing the potential for less bleeding [32,33]. These advantages might have increased their preference among Indian cardiologists.
AUGUSTUS study and ARISTOTLE study demonstrated that apixaban exerted comparable and favorable effects on preventing stroke, systemic embolism, and mortality and caused less major bleeding than warfarin irrespective of aspirin use [7,34]. Moreover, among NOACs, apixaban demonstrated lower rates of both ischemic stroke or systemic embolism and bleeding compared with rivaroxaban in patients with AF [35,36]. In the AUGUSTUS trial, the use of apixaban at a dose of 5 mg BD was shown to be an effective regimen that is superior to VKAs [7]. Thus, 5 mg BD of apixaban (83.22%) with DAPT was the most commonly prescribed dose by cardiologists in our survey.
Our study is limited by a descriptive survey and the responses are from physician reported which may not provide a true representation of patients’ responses.
Conclusions
Our survey demonstrated that the majority of cardiologists used triple therapy (NOAC + dual antiplatelet [aspirin and P2Y12 inhibitor]), followed by NOAC + single antiplatelet for managing patients with AF and ACS or undergoing PCI in line with the available guidelines. NOACs were the preferred anticoagulant among responders in this study. The physician reported patient adherence rates to NOACs were higher compared to VKAs. 5 mg BD of apixaban with DAPT was the most commonly prescribed dose by cardiologists in our survey. Among P2Y12 inhibitors, ticagrelor and clopidogrel were the most preferred medication. The majority of cardiologists reportedly changed antiplatelet therapy for patients from dual antiplatelet to single antiplatelet therapy in three months, followed by cardiologists in one month, and a very small proportion of cardiologists in six months. A maximum number of cardiologists stopped prescribing antiplatelet therapy for patients by one year.
Acknowledgments
CBCC were paid consultants to Pfizer Ltd., India, in connection with the development of this manuscript. Additional editorial support was provided by Axa Jacob (Medical Excellence, Emerging Markets, Pfizer Ltd.).
The content published in Cureus is the result of clinical experience and/or research by independent individuals or organizations. Cureus is not responsible for the scientific accuracy or reliability of data or conclusions published herein. All content published within Cureus is intended only for educational, research and reference purposes. Additionally, articles published within Cureus should not be deemed a suitable substitute for the advice of a qualified health care professional. Do not disregard or avoid professional medical advice due to content published within Cureus.
The authors have declared financial relationships, which are detailed in the next section.
Namrata Kulkarni, Santosh Taur, Jaspreet Kaur, Ravishankar Akolekar, Swetha E S declare(s) employment from Pfizer Ltd. All the listed Authors are paid employees of Pfizer Ltd., India and have provided the editorial support in the manuscript development.
Human Ethics
Consent was obtained or waived by all participants in this study
Animal Ethics
Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.
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