VTE Registry: What Can Be Learned from RIETE?

被引：23

作者：

Tzoran, Inna ^{[1
]}

Brenner, Benjamin ^{[1
,2
]}

Papadakis, Manolis ^{[3
]}

Di Micco, Pierpaolo ^{[4
]}

Monreal, Manuel ^{[5
]}

机构：

[1] Rambam Hlth Care Campus, Dept Hematol & Bone Marrow Transplantat, Haifa, Israel

[2] Technion Israel Inst Technol, Bruce Rappaport Fac Med, Haifa, Israel

[3] Hosp Papageorg, Dept Hematol, Saloniki, Greece

[4] Osped Buon Consiglio Fatebenefratelli, Dept Internal Med, Naples, Italy

[5] Hosp Badalona Germans Trias & Pujol, Dept Internal Med, Badalona, Spain

来源：

RAMBAM MAIMONIDES MEDICAL JOURNAL | 2014年 / 5卷 / 04期

关键词：

Anticoagulant therapy; outcome; registry; venous thromboembolism;

D O I：

10.5041/RMMJ.10171

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The Registro Informatizado de Enfermedad TromboEmbolica (RIETE Registry) is an ongoing, international, prospective registry of consecutive patients with acute venous thromboembolism (VTE) designed to gather and analyze data on treatment patterns and outcomes in patients with acute VTE. It started in Spain in 2001, and 6 years later the database was translated into English with the aim to expand the Registry to other countries. In contrast to randomized controlled trials, there is no imposed experimental intervention: the management is determined solely by physicians. Thus, it provides data on patients with VTE in a real-world situation with an unselected patient population. Data from RIETE are hypothesis-generating and provide feedback from real-world clinical situations. So far, we learned about the natural history of VTE in patients with relative or absolute contraindications to anticoagulant therapy. We

引用

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