Concurrent Cerebral Amyloid Angiopathy (CAA) and Atrial Fibrillation are becoming an increasingly common dilemma in clinical practice due to the aging population and the comorbidities associated with it. In such patients, the physician must appreciate and strike the difficult balance between the risk of ischemic strokes from atrial fibrillation on one hand, and that of intracerebral hemorrhage from coexisting CAA on the other. Anticoagulation is necessary for the former but potentially deleterious for the latter. In this case report, we present the case of a 67-year-old woman with a long history of atrial fibrillation on rivaroxaban who recently began to experience recurrent transient neurological deficits that were later diagnosed as amyloid spells related to concomitant CAA. While there is no clear-cut consensus in published literature on how to best manage these patients regarding the use of anticoagulation, it is recommended to involve a multidisciplinary team for optimal management of these patients.
Objective
The study aims to review the literature regarding abnormalities predisposing to Sudden Cardiac Death (SCD) in young Middle Eastern and African competitive athletes between the years 2009–2019 and aims to assess cardiac pre-participation screening methods.
Methods
A PubMed search was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The search targeted articles that reported the prevalence of cardiac abnormalities found in Middle Eastern and African athletes, and it also focused on comparing cardiac screening methods for assessment of athletes.
Results
our studies fell within the inclusion criteria and were included in the study. Results identified a shortage in the literature regarding prevalence rates of SCD in the Middle East and Africa. Additionally, there seems to be a lack of ethnicity-specific cardiac pre-participation screening programs in the region. Nevertheless, the prevalence of SCD-related abnormalities (HCM, ARVC, etc …) ranged from 0.47 to 4.29%. Included studies conveyed only male athletes with no reports on the female athletic population.
Conclusion
The present study highlights a need to develop an efficient cardiac pre-participation screening program specific to Arab and African athletes due to their high false-positive rates in contrast to Caucasian athletes. Significant evidence proves that an adequate cardiac screening program can prevent SCD in young competitive athletes. Therefore, it is imperative that future studies highlight the prevalence of abnormalities directly related to SCD in order to create a valid screening program that can be implemented in the region to mitigate the risk of shocking events.
Objectives: The novel Coronavirus (SARS-CoV2) adversely affects cardiac
status and may cause arrhythmias. The objective of this study is to
describe the case of a 41 year-old female presenting to the emergency
department with Right ventricular outflow tract (RVOT) ventricular
tachycardia; as well as to appraise and compare etiologies proposed in
the literature with our case. Methods: The study design is a case report
and review of the literature. A PubMed/Medline search was conducted
including studies published in peer-reviewed journals between December,
2019 and November, 2020. Papers discussing the relationship between
COVID-19 and cardiac arrhythmias were included, excluding the pediatric
population and papers with major confounding factors to the
predisposition of cardiac arrhythmias. Results: 6 papers were included
in the qualitative synthesis. These papers discussed different
mechanisms by which COVID-19 can cause arrhythmias. These results were
compared with the findings in our case in an attempt to better
understand the etiology behind our case of RVOT-VT. Proposed etiologies
included ACE2-mediated direct damage of cardiomyocytes, raised serum CRP
levels, and raised systemic inflammatory markers and activation of the
Ca2+/Calmodulin protein kinase I. Conclusion: The lack of associated
comorbidities and risk factors in our patient highlights the unique
challenge of identifying the clinical sequelae of COVID-19. Proposed
pathophysiologies in the literature were not applicable to our case,
highlighting the need for clinical monitoring in patients, and the need
for further research on the topic.
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