跳至主要内容
临床试验/NL-OMON25616
NL-OMON25616招募中不适用

Pulmonary arteriovenous malformations: strategies for detection, treatment and follow-up.

St. Antonius Hospital0 个研究点目标入组 1,500 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,500

研究概览

简要总结

Recent publications: 1. Velthuis S, Buscarini E, Mager JJ, Vorselaars VMM, van Gent MWF, Gazzaniga P, Manfredi G, Danesino C, Diederik AL, Vos JA, Gandolfi S, Snijder RJ, Westermann CJJ and Post MC. Predicting the size of pulmonary arteriovenous malformations on chest computed tomography: a role for transthoracic contrast echocardiography. European Respiratory Journal 2014; [Epub ahead of print] 2. Vorselaars VMM, Velthuis S, Mager JJ, Snijder RJ, Bos W-J, Vos JA, Strijen MJL and Post MC. Direct haemodynamic effects of pulmonary arteriovenous malformation embolisation. Netherlands Heart Journal 2014; [Epub ahead of print] 3. de Gussem EM, Lausman AY, Beder AJ, Edwards CP, Blanker MH, Terbrugge KG, Mager JJ and Faughnan ME. Outcomes of Pregnancy in Women With Hereditary Hemorrhagic Telangiectasia. Obstetrics & Gynecology 2014; 123(3):514-520 4. van Gent MWF, Velthuis S, Post MC, Snijder RJ, Westermann CJJ, Letteboer TGW and Mager JJ. Hereditary hemorrhagic telangiectasia: how accurate are the clinical criteria? American Journal of Medical Genetics Part A 2013; 161(3):461-466. 5. Velthuis S, Buscarini E, van Gent MW, Gazzaniga P, Manfredi G, Danesino C, Schonewille WJ, Westermann CJ, Snijder RJ, Mager JJ and Post MC. Grade of pulmonary right-to-left shunt on contrast echocardiography and cerebral complications; a striking association. Chest 2013; 144(2):542-548. 6. Velthuis S, Vorselaars VM, van Gent MW, Westermann CJ, Snijder RJ, Mager JJ and Post MC. Role of transthoracic contrast echocardiography in the clinical diagnosis of hereditary hemorrhagic telangiectasia. Chest 2013; 144(6):1876-1882.

入排标准

入选标准

  • All consecutive persons screened for HHT and/or PAVMs from 2004 until present at the St.
  • Antonius Hospital will be included in the dataset.

排除标准

  • Patients without HHT and without PAVMs and no family history of HHT

研究者

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