Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Background: Even though ticagrelor was beneficial in prior cardiovascular trials, its efficacy in stroke prevention was inconclusive in recent randomized-controlled clinical trials (RCTs). We sought to consolidate the evidence for efficacy and safety of ticagrelor for stroke prevention.
Methods: We conducted a systematic review and meta-analysis of RCTs in major databases reporting following efficacy and safety outcomes among patients with cerebral or cardiovascular risk factors treated with ticagrelor (vs. control): ischemic stroke (IS), combined ischemic and hemorrhagic stroke, myocardial infarction (MI), cardiovascular death (CVD), all-cause mortality, and major bleeding events. We pooled risk ratios (RR) and adjusted hazard ratios (HR) from each trial using random-effect models, and assessed the heterogeneity using Cochran Q and I statistics.
Results: We identified 13 RCTs, comprising 64,360 patients. In comparison to control group, ticagrelor reduced the risk of IS (RR = 0.86; 95%CI = 0.78-0.95, p = .003; I = 0%), combined ischemic and hemorrhagic strokes (risk ratio: 0.90; 95%CI: 0.81-1.00, p = .05; I = 0%), and composite stroke/MI/CVD (RR = 0.90; 95%CI = 0.81-0.99, p = .03; I = 47%). Ticagrelor was not associated with increased risk of mortality (RR: 0.95; 95%CI: 0.84-1.07; p = .40) or major bleeding events (RR: 1.18; 95%CI: 0.92-1.50; p = .19). Additional analyses demonstrated that ticagrelor reduced the risk of incident strokes (HR = 0.87; 95%CI = 0.76-0.98; p = .03) and composite stroke/MI/CVD (HR = 0.88; 95%CI = 0.78-0.98; p = .02) among patients with prior history of IS or transient ischemic attack.
Conclusions: Ticagrelor seems to be a beneficial option for primary and secondary stroke prevention in patients with cerebral or cardiovascular risk factors. Further RCTs are needed to evaluate the role of ticagrelor in secondary stroke prevention.
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Source |
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http://dx.doi.org/10.1016/j.jns.2018.05.001 | DOI Listing |
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