13 results on '"Hoven, A.T. van den"'
Search Results
2. Aortic dilation and growth in women with Turner syndrome.
- Author
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Meccanici, F., Schotte, M.H., Snoeren, M.M., Bons, L.R., Hoven, A.T. van den, Kardys, I., Budde, Ricardo P.J., Bosch, A.E. van den, Duijnhouwer, A.L., Roos-Hesselink, J.W., Meccanici, F., Schotte, M.H., Snoeren, M.M., Bons, L.R., Hoven, A.T. van den, Kardys, I., Budde, Ricardo P.J., Bosch, A.E. van den, Duijnhouwer, A.L., and Roos-Hesselink, J.W.
- Abstract
Item does not contain fulltext
- Published
- 2022
3. Blood biomarkers in patients with bicuspid aortic valve disease
- Author
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Bons, Lidia R., Geenen, Laurie W., Hoven, A.T. van den, Dik, Willem A., Bosch, A.E. van den, Duijnhouwer, A.L., Loeys, B.L., Roos-Hesselink, J.W., Bons, Lidia R., Geenen, Laurie W., Hoven, A.T. van den, Dik, Willem A., Bosch, A.E. van den, Duijnhouwer, A.L., Loeys, B.L., and Roos-Hesselink, J.W.
- Abstract
Contains fulltext : 221673.pdf (Publisher’s version ) (Closed access)
- Published
- 2020
4. Blood biomarkers in patients with bicuspid aortic valve disease
- Author
-
Bons, Lidia R., Geenen, Laurie W., Hoven, A.T. van den, Dik, Willem A., Bosch, A.E. van den, Duijnhouwer, A.L., Loeys, B.L., Roos-Hesselink, J.W., Bons, Lidia R., Geenen, Laurie W., Hoven, A.T. van den, Dik, Willem A., Bosch, A.E. van den, Duijnhouwer, A.L., Loeys, B.L., and Roos-Hesselink, J.W.
- Abstract
Contains fulltext : 221673.pdf (Publisher’s version ) (Closed access)
- Published
- 2020
5. Intermodality variation of aortic dimensions: How, where and when to measure the ascending aorta
- Author
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Bons, L.R., Duijnhouwer, A.L., Boccalini, S., Hoven, A.T. van den, Vlugt, M.J. van der, Chelu, R.G., McGhie, J.S., Kardys, I., Bosch, A.E. van den, Siebelink, H.J., Nieman, K., Hirsch, A., Broberg, C.S., Budde, R.P., Roos-Hesselink, J.W., Bons, L.R., Duijnhouwer, A.L., Boccalini, S., Hoven, A.T. van den, Vlugt, M.J. van der, Chelu, R.G., McGhie, J.S., Kardys, I., Bosch, A.E. van den, Siebelink, H.J., Nieman, K., Hirsch, A., Broberg, C.S., Budde, R.P., and Roos-Hesselink, J.W.
- Abstract
Item does not contain fulltext, BACKGROUND: No established reference-standard technique is available for ascending aortic diameter measurements. The aim of this study was to determine agreement between modalities and techniques. METHODS: In patients with aortic pathology transthoracic echocardiography, computed tomography angiography (CTA) and magnetic resonance angiography (MRA) were performed. Aortic diameters were measured at the sinus of Valsalva (SoV), sinotubular junction (STJ) and tubular ascending aorta (TAA) during mid-systole and end-diastole. In echocardiography both the inner edge-to-inner edge (I-I edge) and leading edge-toleading edge (L-L edge) methods were applied, and the length of the aortic annulus to the most cranial visible part of the ascending aorta was measured. In CTA and MRA the I-I method was used. RESULTS: Fifty patients with bicuspid aortic valve (36+/-13years, 26% female) and 50 Turner patients (35+/-13years) were included. Comparison of all aortic measurements showed a mean difference of 5.4+/-2.7mm for the SoV, 5.1+/-2.0mm for the STJ and 4.8+/-2.1mm for the TAA. The maximum difference was 18mm. The best agreement was found between echocardiography L-L edge and CTA during mid-systole. CTA and MRA showed good agreement. A mean difference of 1.5+/-1.3mm and 1.8+/-1.5mm was demonstrated at the level of the STJ and TAA comparing mid-systolic with end-diastolic diameters. The visible length of the aorta increased on average 5.3+/-5.1mmW during mid-systole. CONCLUSIONS: MRA and CTA showed best agreement with L-L edge method by echocardiography. In individual patients large differences in ascending aortic diameter were demonstrated, warranting measurement standardization. The use of CTA or MRA is advised at least once.
- Published
- 2019
6. Intermodality variation of aortic dimensions: How, where and when to measure the ascending aorta
- Author
-
Bons, L.R., Duijnhouwer, A.L., Boccalini, S., Hoven, A.T. van den, Vlugt, M.J. van der, Chelu, R.G., McGhie, J.S., Kardys, I., Bosch, A.E. van den, Siebelink, H.J., Nieman, K., Hirsch, A., Broberg, C.S., Budde, R.P., Roos-Hesselink, J.W., Bons, L.R., Duijnhouwer, A.L., Boccalini, S., Hoven, A.T. van den, Vlugt, M.J. van der, Chelu, R.G., McGhie, J.S., Kardys, I., Bosch, A.E. van den, Siebelink, H.J., Nieman, K., Hirsch, A., Broberg, C.S., Budde, R.P., and Roos-Hesselink, J.W.
- Abstract
Item does not contain fulltext, BACKGROUND: No established reference-standard technique is available for ascending aortic diameter measurements. The aim of this study was to determine agreement between modalities and techniques. METHODS: In patients with aortic pathology transthoracic echocardiography, computed tomography angiography (CTA) and magnetic resonance angiography (MRA) were performed. Aortic diameters were measured at the sinus of Valsalva (SoV), sinotubular junction (STJ) and tubular ascending aorta (TAA) during mid-systole and end-diastole. In echocardiography both the inner edge-to-inner edge (I-I edge) and leading edge-toleading edge (L-L edge) methods were applied, and the length of the aortic annulus to the most cranial visible part of the ascending aorta was measured. In CTA and MRA the I-I method was used. RESULTS: Fifty patients with bicuspid aortic valve (36+/-13years, 26% female) and 50 Turner patients (35+/-13years) were included. Comparison of all aortic measurements showed a mean difference of 5.4+/-2.7mm for the SoV, 5.1+/-2.0mm for the STJ and 4.8+/-2.1mm for the TAA. The maximum difference was 18mm. The best agreement was found between echocardiography L-L edge and CTA during mid-systole. CTA and MRA showed good agreement. A mean difference of 1.5+/-1.3mm and 1.8+/-1.5mm was demonstrated at the level of the STJ and TAA comparing mid-systolic with end-diastolic diameters. The visible length of the aorta increased on average 5.3+/-5.1mmW during mid-systole. CONCLUSIONS: MRA and CTA showed best agreement with L-L edge method by echocardiography. In individual patients large differences in ascending aortic diameter were demonstrated, warranting measurement standardization. The use of CTA or MRA is advised at least once.
- Published
- 2019
7. Adverse outcome of coarctation stenting in patients with Turner syndrome
- Author
-
Hoven, A.T. van den, Duijnhouwer, A.L., Eicken, A., Aboulhosn, J., Bruin, C. de, Backeljauw, P.F., Demulier, L., Chessa, M., Uebing, A., Veldtman, G.R., Armstrong, A.K., Bosch, A.E. van den, Witsenburg, M., Roos-Hesselink, J.W., Hoven, A.T. van den, Duijnhouwer, A.L., Eicken, A., Aboulhosn, J., Bruin, C. de, Backeljauw, P.F., Demulier, L., Chessa, M., Uebing, A., Veldtman, G.R., Armstrong, A.K., Bosch, A.E. van den, Witsenburg, M., and Roos-Hesselink, J.W.
- Abstract
Item does not contain fulltext, OBJECTIVES: This study examines the outcome and procedural outcomes of percutaneous stent angioplasty for aortic coarctation in patients with Turner syndrome (TS). BACKGROUND: TS occurs in 1 in 2,500 live-born females and is associated with aortic coarctation. METHODS: In this multicenter, retrospective cohort study, all patients with TS and a coarctation of the aorta, treated with percutaneous stent implantation were included. The procedural strategies were dictated by local protocols. Adverse events at short- and long-term follow-up and qualitative parameters concerning the stent implantation were assessed. RESULTS: In the largest study to date of TS patients receiving aortic stents, a total of 19 patients from 10 centers were included. Twelve patients were treated for native and 7 for recurrent coarctation. Age at intervention was 16.9 (7-60) years (median; min-max). The coarctation diameter increased significantly from 8.0 mm (2-12) pre-intervention to 15.0 mm (10-19) post-intervention (P < 0.001). Three (15.8%) adverse events occurred within 30 days of the procedure, including two dissections despite the use of covered stents, one resulting in death. At long-term follow-up (6.5 years, min-max: 1-16), two additional deaths occurred not known to be stent-related. CONCLUSIONS: Though percutaneous treatment of aortic coarctation in TS patients is effective, it is associated with serious morbidity and mortality. These risks suggest that alternative treatment options should be carefully weighed against percutaneous stenting strategies. (c) 2016 Wiley Periodicals, Inc.
- Published
- 2017
8. Partial anomalous pulmonary venous return in Turner syndrome
- Author
-
Hoven, A.T. van den, Chelu, R.G., Duijnhouwer, A.L., Demulier, L., Devos, D., Nieman, K., Witsenburg, M., Bosch, A.E. van den, Loeys, B.L., Hagen, I.M. van, Roos-Hesselink, J.W., Hoven, A.T. van den, Chelu, R.G., Duijnhouwer, A.L., Demulier, L., Devos, D., Nieman, K., Witsenburg, M., Bosch, A.E. van den, Loeys, B.L., Hagen, I.M. van, and Roos-Hesselink, J.W.
- Abstract
Item does not contain fulltext, PURPOSE: The aim of this study is to describe the prevalence, anatomy, associations and clinical impact of partial anomalous pulmonary venous return in patients with Turner syndrome. METHODS AND RESULTS: All Turner patients who presented at our Turner clinic, between January 2007 and October 2015 were included in this study and underwent ECG, echocardiography and advanced imaging such as cardiac magnetic resonance or computed tomography as part of their regular clinical workup. All imaging was re-evaluated and detailed anatomy was described. Partial anomalous pulmonary venous return was diagnosed in 24 (25%) out of 96 Turner patients included and 14 (58%) of these 24 partial anomalous pulmonary venous return had not been reported previously. Right atrial or ventricular dilatation was present in 11 (46%) of 24 partial anomalous pulmonary venous return patients. CONCLUSION: When studied with advanced imaging modalities and looked for with specific attention, PAPVR is found in 1 out of 4 Turner patients. Half of these patients had right atrial and/or ventricular dilatation. Evaluation of pulmonary venous return should be included in the standard protocol in all Turner patients.
- Published
- 2017
9. Adverse outcome of coarctation stenting in patients with Turner syndrome
- Author
-
Hoven, A.T. van den, Duijnhouwer, A.L., Eicken, A., Aboulhosn, J., Bruin, C. de, Backeljauw, P.F., Demulier, L., Chessa, M., Uebing, A., Veldtman, G.R., Armstrong, A.K., Bosch, A.E. van den, Witsenburg, M., Roos-Hesselink, J.W., Hoven, A.T. van den, Duijnhouwer, A.L., Eicken, A., Aboulhosn, J., Bruin, C. de, Backeljauw, P.F., Demulier, L., Chessa, M., Uebing, A., Veldtman, G.R., Armstrong, A.K., Bosch, A.E. van den, Witsenburg, M., and Roos-Hesselink, J.W.
- Abstract
Item does not contain fulltext, OBJECTIVES: This study examines the outcome and procedural outcomes of percutaneous stent angioplasty for aortic coarctation in patients with Turner syndrome (TS). BACKGROUND: TS occurs in 1 in 2,500 live-born females and is associated with aortic coarctation. METHODS: In this multicenter, retrospective cohort study, all patients with TS and a coarctation of the aorta, treated with percutaneous stent implantation were included. The procedural strategies were dictated by local protocols. Adverse events at short- and long-term follow-up and qualitative parameters concerning the stent implantation were assessed. RESULTS: In the largest study to date of TS patients receiving aortic stents, a total of 19 patients from 10 centers were included. Twelve patients were treated for native and 7 for recurrent coarctation. Age at intervention was 16.9 (7-60) years (median; min-max). The coarctation diameter increased significantly from 8.0 mm (2-12) pre-intervention to 15.0 mm (10-19) post-intervention (P < 0.001). Three (15.8%) adverse events occurred within 30 days of the procedure, including two dissections despite the use of covered stents, one resulting in death. At long-term follow-up (6.5 years, min-max: 1-16), two additional deaths occurred not known to be stent-related. CONCLUSIONS: Though percutaneous treatment of aortic coarctation in TS patients is effective, it is associated with serious morbidity and mortality. These risks suggest that alternative treatment options should be carefully weighed against percutaneous stenting strategies. (c) 2016 Wiley Periodicals, Inc.
- Published
- 2017
10. Partial anomalous pulmonary venous return in Turner syndrome
- Author
-
Hoven, A.T. van den, Chelu, R.G., Duijnhouwer, A.L., Demulier, L., Devos, D., Nieman, K., Witsenburg, M., Bosch, A.E. van den, Loeys, B.L., Hagen, I.M. van, Roos-Hesselink, J.W., Hoven, A.T. van den, Chelu, R.G., Duijnhouwer, A.L., Demulier, L., Devos, D., Nieman, K., Witsenburg, M., Bosch, A.E. van den, Loeys, B.L., Hagen, I.M. van, and Roos-Hesselink, J.W.
- Abstract
Item does not contain fulltext, PURPOSE: The aim of this study is to describe the prevalence, anatomy, associations and clinical impact of partial anomalous pulmonary venous return in patients with Turner syndrome. METHODS AND RESULTS: All Turner patients who presented at our Turner clinic, between January 2007 and October 2015 were included in this study and underwent ECG, echocardiography and advanced imaging such as cardiac magnetic resonance or computed tomography as part of their regular clinical workup. All imaging was re-evaluated and detailed anatomy was described. Partial anomalous pulmonary venous return was diagnosed in 24 (25%) out of 96 Turner patients included and 14 (58%) of these 24 partial anomalous pulmonary venous return had not been reported previously. Right atrial or ventricular dilatation was present in 11 (46%) of 24 partial anomalous pulmonary venous return patients. CONCLUSION: When studied with advanced imaging modalities and looked for with specific attention, PAPVR is found in 1 out of 4 Turner patients. Half of these patients had right atrial and/or ventricular dilatation. Evaluation of pulmonary venous return should be included in the standard protocol in all Turner patients.
- Published
- 2017
11. Partial anomalous pulmonary venous return in Turner syndrome
- Author
-
Hoven, A.T. van den, Chelu, R.G., Duijnhouwer, A.L., Demulier, L., Devos, D., Nieman, K., Witsenburg, M., Bosch, A.E. van den, Loeys, B.L., Hagen, I.M. van, Roos-Hesselink, J.W., Hoven, A.T. van den, Chelu, R.G., Duijnhouwer, A.L., Demulier, L., Devos, D., Nieman, K., Witsenburg, M., Bosch, A.E. van den, Loeys, B.L., Hagen, I.M. van, and Roos-Hesselink, J.W.
- Abstract
Item does not contain fulltext, PURPOSE: The aim of this study is to describe the prevalence, anatomy, associations and clinical impact of partial anomalous pulmonary venous return in patients with Turner syndrome. METHODS AND RESULTS: All Turner patients who presented at our Turner clinic, between January 2007 and October 2015 were included in this study and underwent ECG, echocardiography and advanced imaging such as cardiac magnetic resonance or computed tomography as part of their regular clinical workup. All imaging was re-evaluated and detailed anatomy was described. Partial anomalous pulmonary venous return was diagnosed in 24 (25%) out of 96 Turner patients included and 14 (58%) of these 24 partial anomalous pulmonary venous return had not been reported previously. Right atrial or ventricular dilatation was present in 11 (46%) of 24 partial anomalous pulmonary venous return patients. CONCLUSION: When studied with advanced imaging modalities and looked for with specific attention, PAPVR is found in 1 out of 4 Turner patients. Half of these patients had right atrial and/or ventricular dilatation. Evaluation of pulmonary venous return should be included in the standard protocol in all Turner patients.
- Published
- 2017
12. Adverse outcome of coarctation stenting in patients with Turner syndrome.
- Author
-
Hoven, A.T. van den and Hoven, A.T. van den
- Subjects
- Radboudumc 16: Vascular damage RIHS: Radboud Institute for Health Sciences.
- Published
- 2017
13. Partial anomalous pulmonary venous return in Turner syndrome.
- Author
-
Hoven, A.T. van den and Hoven, A.T. van den
- Subjects
- Radboudumc 16: Vascular damage RIHS: Radboud Institute for Health Sciences., Radboudumc 9: Rare cancers RIHS: Radboud Institute for Health Sciences.
- Published
- 2017
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