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- W2555354408 abstract "Summary. The use of vena caval filters to prevent fatal pulmonary embolism (PE) has become the standard of care for patients who cannot be safely or effec tively anticoagulated. This is due to several factors: improved devices, percuta neous methods of delivery, and long-term experience of safety and efficacy. Six vena caval filters are currently marketed with Food and Drug Administration approval: the Simon Nitinol, VenaTech, Bird's Nest, and three iterations of the Greenfield filter, Each of these devices has been reviewed based upon reports from published clinical studies. This type of summary is complicated by disparity in the study methodologies, numbers of patients, lengths of follow-up, and definition of adverse events. The need for established reporting standards is clear. A consensus document, which is in preparation, should be available in 1999 and should lead to greatly improved reports." @default.
- W2555354408 created "2016-11-30" @default.
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- W2555354408 date "1999-01-01" @default.
- W2555354408 modified "2023-09-27" @default.
- W2555354408 title "Clinical Experience with Vena" @default.
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