Cerebrovascular Disease - Results With Antithrombotic Therapy : Some Observations

1981 ◽  
Author(s):  
B A Sandok

Antithrombotic therapy is now widely used in the treatment of patients with ischemic cerebrovascular disease. Governmental approval will increase use and further convince many that the issues of therapy are now resolved. They are not. The following approved professional labelling guidelines serve to highlight the many clinical and investigational problems that remain: (1) There is evidence that aspirin is safe and effective for reducing the risk of stroke in men who have symptoms due to fibrin-platelet emboli.(2) Patients should have a complete medical and neurologic evaluation.(3) The recommended dosage is 1300 mgm/day.The evidence for effectiveness, while of statistical significance, becomes clinically less important when one notes that in the Canadian study, a disturbing 12.4% of patients under treatment with aspirin, developed subsequent stroke. This should not be unexpected since similar cerebral ischemic symptoms may be produced by differing pathophysiologic mechanisms (not all related to fibrin-platelet embolization); and treatment for one may be illogical and ineffective for another. Accurate diagnosis is imperative for selecting appropriate therapy. In the clinical situation, in spite of “complete” evaluation, uncertainty of the underlying mechanism often remains. Questions also remain about the dosage recommendations, and other treatment alternatives for both women and men.Subsequent clinical trials will need to consider each of the above. Until then, patients with cerebral ischemic symptoms must be evaluated individually. Some may benefit from antithrombotic therapy-many will not.

1991 ◽  
Vol 11 (04) ◽  
pp. 353-367 ◽  
Author(s):  
José Biller ◽  
Betsy Love ◽  
David Gordon

2019 ◽  
Vol 74 (6) ◽  
pp. 786-803 ◽  
Author(s):  
Victor J. Del Brutto ◽  
Seemant Chaturvedi ◽  
Hans-Christoph Diener ◽  
Jose G. Romano ◽  
Ralph L. Sacco

1982 ◽  
Vol 48 (02) ◽  
pp. 117-119 ◽  
Author(s):  
M Kusunoki ◽  
K Kimura ◽  
K Nagatsuka ◽  
Y Isaka ◽  
O Uyama ◽  
...  

SummaryPlatelet aggregation was studied in 24 patients in the chronic stage of ischemic cerebrovascular disease (CVD), with cerebral affluent and effluent blood, i.e., carotid arterial and internal jugular venous blood, and also with peripheral venous blood. Aggregation tests were performed at various final concentrations of sodium arachidonate (A.A.) and ADP. In 17 patients, not taking aspirin, platelet aggregability in jugular venous blood was significantly accentuated compared with that in arterial and peripheral venous blood. This tendency was more marked in the patients with cerebral artery stenosis and/or occlusion than in those with normal cerebral angiogram. In 7 patients taking 500 mg or more oral aspirin, aggregation differences across the brain were not observed and A.A. aggregation and the second phase of ADP aggregation were completely suppressed. These results suggest that a prophylactic administration of aspirin may be beneficial for patients in chronic stage of CVD.


Author(s):  
Khalaf Kridin ◽  
Jennifer E. Hundt ◽  
Ralf J. Ludwig ◽  
Kyle T. Amber ◽  
Dana Tzur Bitan ◽  
...  

AbstractThe association between bullous pemphigoid (BP) and melanoma is yet to be investigated. We aimed to assess assess the bidirectional association between BP and melanoma and to delineate the epidemiological features of patients with both diagnoses. A population-based cohort study was performed comparing BP patients (n = 3924) with age-, sex- and ethnicity-matched control subjects (n = 19,280) with regard to incident cases of melanoma. A case–control design was additionally adopted to estimate the risk of BP in individuals with a preexisting diagnosis of melanoma. The prevalence of preexisting melanoma was higher in patients with BP than in control subjects (1.5% vs. 1.0%, respectively; P = 0.004). A history of melanoma confers a 50% increase in the risk of subsequent BP (OR 1.53; 95% CI 1.14–2.06). This risk was higher among males (OR 1.66; 95% CI 1.09–2.54) and individuals older than 80 years (OR 1.63; 95% CI 1.11–2.38), and persisted after adjustment for multiple putative confounders including PD-1/PDL-1 antagonists (adjusted OR 1.53; 95% CI 1.14–2.06). Conversely, the risk of melanoma among patients with BP was slightly elevated, but did not reach the level of statistical significance (adjusted HR 1.13; 95% CI 0.73–1.74). Patients with a dual diagnosis of BP and melanoma were older at the onset of BP and had lower body mass index. A history of melanoma is associated with a 50% increase in the incidence of subsequent BP. Physicians managing patients with both conditions should be aware of this association. Further research is warranted to reveal the underlying mechanism of these findings.


1987 ◽  
Vol 27 (6) ◽  
pp. 511-518
Author(s):  
Osamu SASAKI ◽  
Tetsuo KOIKE ◽  
Shigeaki OHSUGI ◽  
Shigekazu TAKEUCHI ◽  
Ryuichi TANAKA ◽  
...  

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