Optimal postprocedural antithrombotic regimen is uncertain after transcatheter aortic valve replacement (TAVR). We developed an online questionnaire on post-TAVR antithrombotic management. After research ethics board approval, we distributed the survey to TAVR implanters across Canada. A total of 24 TAVR implanters from 17 centres responded to the survey for a response rate of 75%. Dual antiplatelet therapy for variable durations was the preferred initial treatment for patients in sinus rhythm after isolated TAVR, TAVR with a recent stent (≤ 1 month), and valve-in-valve procedures (71%, 96%, and 65%, respectively). Most respondents continued patients on acetylsalicylic acid indefinitely after these procedures (100%, 92%, 90%, respectively). In patients with atrial fibrillation, the CHA2DS2-VASC score was the preferred stroke risk score for 57% of respondents, the CHADS2 score was the preferred stroke risk score for 22% of respondents, and the CHADS65 score was the preferred stroke risk score for 17% of respondents. To determine the risk of bleeding, the HASBLED score was most often used (52%), but 48% of respondents indicated that they did not use a bleeding risk score. In the presence of atrial fibrillation, antithrombotic therapy choice varied widely. Our survey shows that dual antiplatelet therapy is the most common discharge regimen after TAVR in current practice. However, the choice and duration of antithrombotic regimen vary in patients requiring anticoagulation. 相似文献
方法:计算机检索PubMed、Embase、Cochrane图书馆、Web of Science、CBM、 CNKI、CQVIP、CECDB数据库内的相关前瞻性或回顾性临床对照试验,检索时限均为从建库起截止2019-08。由两位研究者独立筛选文献、提取资料、评价文献质量,采用RevMan5.3/Stata 14.0软件对纳入研究进行meta分析。
Aim: In Western European populations, about 18% of all individuals have a complete deficiency of the alpha‐actinin‐3 protein owing to homozygosity for a stop codon mutation (R577X) in the ACTN3 gene. Actn3?/? knock‐out mice show increased activity of multiple enzymes in the aerobic metabolic pathway in fast muscle fibres. Whether this observation is also present in human XX genotype carriers compared to RR carriers has not been studied in a fibre‐type‐specific approach in humans. The purpose of this study was therefore to compare fibre‐type‐specific oxidative enzyme activity in humans with a different ACTN3 R577X genotype. Methods: Vastus lateralis muscle biopsy samples of 17 XX and 16 RR subjects were used to measure markers of oxidative capacity [cytochrome c oxidase (CYTOX) and succinate dehydrogenase (SDH)] in a fibre‐type‐specific assay using enzyme histochemistry. Results: Cytochrome c oxidase staining showed no significant genotype group differences in type I or type II muscle fibres. Also, we found no significant differences in SDH staining of fast fibres comparing XX and RR carriers. Conclusion: In conclusion, the increase in oxidative enzyme activity of fast muscle fibres, as reported in an Actn3?/? knock‐out mouse, was not observed in our human samples. Known differences in metabolic characteristics of muscle fibres in rodents compared to humans may in part explain this discrepancy in findings. 相似文献