Atrial fibrillation (AF) is the most common arrhythmia in adults. The currently estimated prevalence of AF in adults ranges from 2 to 4%, and a 2.3-fold rise is expected due to the longevity in the general population and the increased screening of patients with previously undiagnosed AF (1). Advanced age is widely regarded as a foremost risk factor, but increasing burden of other comorbidities including hypertension, diabetes mellitus, heart failure, coronary artery disease, chronic kidney disease, obesity, and obstructive sleep apnea also contributes to the higher prevalence of AF. Not only that, many modifiable risk factors are potent contributors to AF development and progression (2). Many cardiovascular and cerebrovascular complications, such as 5-fold rise in stroke and 2 times the risk of mortality, are prevalently screened in patients with AF (3). AF-associated thromboembolic events are lead contributors for the poor prognosis in patients with AF, which involves higher morbidity and mortality (4, 5). Antithrombotic therapy effectively reduces the incidence of embolism in patients with AF. Direct oral anticoagulants (DOACs) have superior effectiveness and safety outcome for the prevention of stroke and thromboembolic events in patients with AF (6). DOACs are recommended as preferred alternatives to warfarin in the American College of Cardiology and/or American Heart Association/Heart Rhythm Society (7) and European Society of Cardiology guidelines (8) due to its superior characteristics in effectiveness, safety, and convenience, especially for elderly patients with acute coronary syndrome or chronic kidney disease (9, 10). Important differences in clinical characteristics, response to treatment, and outcomes of patients with AF distribute to the diverse regions of the world. In Latin America, AF is regarded as a considerable cause of high mortality and disability (11). Although prevalence data is limited, the incidence of AF-related stroke and associated morbidity is increasing in this region (12), and anticoagulation is underused (13). Therefore, patients with AF in Latin America undergo higher risk of death and thromboembolic events due to the aging population and poorly managed risk factors of AF, such as hypertension, diabetes, heart failure, etc. The anticoagulant treatment of patients with AF is particularly significant in Latin America.

Several previously published studies demonstrated that patients with AF in Latin America treated with warfarin had higher adjusted mortality rates and incidence of stroke and/or systemic embolism, intracranial hemorrhage, and life-threatening or fatal bleeding compared with patients with AF in the rest of the world (ROW) (14). Data regarding the effectiveness and safety outcome of anticoagulation regimens in this region is insufficient. Although several new post-hoc analyses of randomized clinical trials (RCTs) well-examined the association between regions (Latin America vs. non-Latin America) and effectiveness and safety outcomes, even explored the use of individual DOACs compared with warfarin in Latin American patients, the superiority of DOACs therapy is still controversial. Although, a previous meta-analysis included the post-hoc analyses and sub-analyses of DOACs, RCTs identified a non-inferiority of DOACs compared with warfarin in Latin American patients with AF (15). However, the RCTs included in this meta-analysis are outdated. New RCTs have been published in recent years and report more endpoint events and even find different results. Therefore, we aimed to reassess the effectiveness and safety outcomes of DOACs vs. warfarin in Latin American and non-Latin American patients with AF.

The process of the literature retrieval is presented in Supplementary Figure 1. A total of 170 studies were identified through the electronic searches in the PubMed and Embase databases. According to the predefined criteria, we finally included 4 studies in this meta-analysis (14, 17–19). Table 1 shows the baseline patient characteristics of the included studies. All include studies are hoc RCT and the data sources are from effective anticoagulation with factor Xa next generation atrial fibrillation–thrombolysis in myocardial infarction 48 (ENGAGE AF-TIMI 48) (14), apixaban for reduction in stroke and other thromboembolic events in atrial fibrillation trial (ARISTOTLE TRIAL) (17), rivaroxaban once daily oral direct factor Xa inhibition compared with vitamin K antagonism for prevention of stroke and embolism trial in atrial fibrillation (ROCKET AF trial) (18), and randomized evaluation of long-term anticoagulant therapy (RE-LY) (19). Latin American includes Argentina Brazil, Chile, Colombia, Mexico, Peru, and Venezuela, and all the remaining countries included in the entire trial were considered to be non-LA countries. In total, 8,965 Latin American patients (5,096 taking DOACs and 3,869 taking warfarin) and 62,716 non-Latin American patients (37,315 taking DOACs and 25,401 taking warfarin) were included in this meta-analysis. All of these included studies had a moderate-to-high quality with the NOS score of ≥6 points.

The main findings of our study were as follows: (1) DOAC use resulted in lower rates of SSE, stroke, hemorrhagic stroke, all-cause death, and associated with safer profiles (lower major or NMCR bleeding, major bleeding, ICH, and any bleeding) than warfarin in Latin American patients with AF; (2) DOAC use resulted in lower rates of SSE, hemorrhagic stroke, all-cause death, cardiovascular death, and associated with safer profiles (lower major or NMCR bleeding, major bleeding, ICH, and any bleeding) than warfarin in non-Latin American patients with AF; (3) DOAC use increased the risk of myocardial infarction than warfarin in non-Latin American patients with AF, but not in Latin American patients with AF; (4) in comparison to VKAs, DOACs were non-inferior regarding the outcomes of ischemic stroke, cardiovascular death, and gastrointestinal bleeding in Latin American patients with AF and the outcomes of stroke, ischemic stroke, and gastrointestinal bleeding in non- Latin American patients.

Important differences in clinical characteristics, response to treatment, and outcomes of patients with AF exist in the diverse regions of the world. Previous studies have shown that Latin American patients with AF are suffering from higher risks of death and embolism than non-Latin American patients with AF (20, 21). Actually, there are many reasons for the increased risk of death and embolism in Latin American patients with AF. Life expectancy differed substantially across cities within the same country. Cause-specific mortality also varied across cities, with some causes of death (unintentional and violent injuries and deaths) showing large variation within countries, whereas other causes of death (communicable, maternal, neonatal and nutritional, cancer, cardiovascular disease, and other non-communicable diseases) varied substantially between countries. These results highlight considerable heterogeneity in life expectancy and causes of death across cities of Latin America (22). Moreover, heterogeneity of risk factors (23–25) and socioeconomic conditions, public awareness, and availability of healthcare services that influence outcomes of diseases differ substantially between countries (26, 27) in Latin America and still need to be taken into account. Furthermore, inadequate prescription for medications associated with death reduction might also affect the prognosis of Latin American patients with AF (14). Therefore, antithrombotic therapy is particularly important to reduce the risk of embolism in Latin American patients with AF. Previous meta-analyses including the post-hoc analyses and sub-analyses of DOAC RCTs showed that there is a non-inferiority of DOACs compared with warfarin in Latin American patients with AF (15). Compared to the previous study, the RCTs included in this meta-analysis are outdated. More importantly, the number of available clinical studies are small and the results are controversial. In recent years, several new post-hoc analyses of RCTs not only examined the association between region and efficacy and safety outcomes but also explored the use of individual DOACs compared with warfarin in Latin American patients. The RCTs provide more endpoint events and arrive at different conclusions. Therefore, we aimed to reassess the effectiveness and safety outcomes of DOACs vs. warfarin in Latin American and non-Latin American patients with AF. Our meta-analysis shows that DOACs appeared to have significant reductions in SSE, stroke, hemorrhagic stroke, all-cause death, major or NMCR bleeding, major bleeding, ICH, and any bleeding, but showed comparable rates of ischemic stroke, cardiovascular death, and gastrointestinal bleeding in Latin American patients with AF. DOACs appeared to have significant reductions in SSE, hemorrhagic stroke, all-cause death, cardiovascular death, major or NMCR bleeding, major bleeding, ICH, and any bleeding and increased the risk of myocardial infarction, but comparable risks of stroke, ischemic stroke, and gastrointestinal bleeding in non-Latin American patients with AF. In addition, we assessed crude event rates of outcomes between DOACs vs. warfarin in Latin/non-Latin American patients with AF. Overall, in comparison to warfarin, DOACs had lower or similar rates of thromboembolic and bleeding risk, which was consistent with a previous study (15). Interestingly, we found that DOACs increased the risk of myocardial infarction compared with warfarin in non-Latin American patients with AF. The result was derived from the RE-LY study, which included patients using dabigatran. Previous studies have warned this risk (28, 29). Prospective data on dabigatran in this population undergoing PCI are still needed.

It is worth pointing out that DOACs have advantages over warfarin such as short onset time, short half-life, low inter- and intra-individual variability, and drug-drug interactions. The current international guidelines recommend the use of DOACs as replacement therapy for VKAs in patients with non-valvular AF because it has more effective, safer, and more convenient features. Different from DOACs, the anticoagulant activity of VKAs depends on TTR (time in therapeutic range). Among the included studies, the mean TTR of VKAs users in Latin America ranged from 58 to 66%, which was not higher than that of non-Latin Americans overall and lower than what is recommended in the guidelines (1, 30). Therefore, DOACs may be regarded as a safer alternative to VKAs in Latin American patients with AF. Although no observational studies have been carried out to directly compare the use of DOACs and warfarin in Latin American patients with AF, several studies have validated the benefits of the use of DOACs in this population. Data from the GLORIA-AF (Global Registry on Long-Term Antithrombotic Treatment in Patients with Atrial Fibrillation, Phase II) study indicated the consistent safety and effectiveness of dabigatran in Latin American patients with AF during a 2-years follow-up (31). Moreover, the XANTUS-EL (Xarelto for Prevention of Stroke in Patients With Atrial Fibrillation in Eastern Europe, the Middle East and Africa [EEMEA], and Latin America) study confirmed the benefits of rivaroxaban for stroke prevention in patients with non-valvular AF from Eastern Europe, the Middle East, Africa, and Latin America (32). However, the results concerning whether DOACs are more cost-effective than warfarin in Latin America remain a controversy (33). The evidence provided by our meta-analysis may offer some confidence to clinicians when selecting DOACs for Latin American patients who need anticoagulation therapy, especially for those at a high risk of bleeding. The present results support that the use of DOACs is at least non-inferior to warfarin in Latin American patients with AF and provides an effective anticoagulant choice without monitoring. Further studies should be performed to clarify this problem.

The current pooled data from the four post-hoc analyses of RCTs suggested that compared with warfarin, DOACs appeared to have significant reductions in SSE, stroke, hemorrhagic stroke, all-cause death, major or NMCR bleeding, major bleeding, ICH, and any bleeding, but comparable risks of ischemic stroke, cardiovascular death, and gastrointestinal bleeding in Latin American patients with AF. DOACs appeared to have significant reductions in SSE, hemorrhagic stroke, all-cause death, cardiovascular death, major or NMCR bleeding, major bleeding, ICH, and any bleeding, and increased the risk of myocardial infarction, but comparable risks of stroke, ischemic stroke, and gastrointestinal bleeding in non-Latin American patients with AF.

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