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Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications
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| Zeitschriftentitel: | Acta Ophthalmologica Scandinavica |
|---|---|
| Personen und Körperschaften: | , , , , |
| In: | Acta Ophthalmologica Scandinavica, 85, 2007, 6, S. 623-630 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Wiley
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| Schlagwörter: |
| author_facet |
Joussen, Antonia M. Kirchhof, Bernd Schrage, Norbert Ocklenburg, Christina Hilgers, Ralf‐Dieter Joussen, Antonia M. Kirchhof, Bernd Schrage, Norbert Ocklenburg, Christina Hilgers, Ralf‐Dieter |
|---|---|
| author |
Joussen, Antonia M. Kirchhof, Bernd Schrage, Norbert Ocklenburg, Christina Hilgers, Ralf‐Dieter |
| spellingShingle |
Joussen, Antonia M. Kirchhof, Bernd Schrage, Norbert Ocklenburg, Christina Hilgers, Ralf‐Dieter Acta Ophthalmologica Scandinavica Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications Ophthalmology |
| author_sort |
joussen, antonia m. |
| spelling |
Joussen, Antonia M. Kirchhof, Bernd Schrage, Norbert Ocklenburg, Christina Hilgers, Ralf‐Dieter 1395-3907 1600-0420 Wiley Ophthalmology http://dx.doi.org/10.1111/j.1600-0420.2007.00898.x <jats:title>Abstract.</jats:title><jats:p><jats:bold>Purpose: </jats:bold> Proliferative vitreoretinopathy (PVR) is the most important reason for blindness following retinal detachment. Presently, vitreous tamponades such as gas or silicone oil cannot contact the lower part of the retina. A heavier‐than‐water tamponade displaces the inflammatory and PVR‐stimulating environment from the inferior area of the retina. The Heavy Silicone Oil versus Standard Silicone Oil Study (HSO Study) is designed to answer the question of whether a heavier‐than‐water tamponade improves the prognosis of eyes with PVR of the lower retina.</jats:p><jats:p><jats:bold>Methods: </jats:bold> The HSO Study is a multicentre, randomized, prospective controlled clinical trial comparing two endotamponades within a two‐arm parallel group design. Patients with inferiorly and posteriorly located PVR are randomized to either heavy silicone oil or standard silicone oil as a tamponading agent. Three hundred and fifty consecutive patients are recruited per group. After intraoperative re‐attachment, patients are randomized to either standard silicone oil (1000 cSt or 5000 cSt) or Densiron<jats:sup>®</jats:sup> as a tamponading agent. The main endpoint criteria are complete retinal attachment at 12 months and change of visual acuity (VA) 12 months postoperatively compared with the preoperative VA. Secondary endpoints include complete retinal attachment before endotamponade removal, quality of life analysis and the number of retina affecting re‐operation within 1 year of follow‐up.</jats:p><jats:p><jats:bold>Results: </jats:bold> The design and early recruitment phase of the study are described.</jats:p><jats:p><jats:bold>Conclusions: </jats:bold> The results of this study will uncover whether or not heavy silicone oil improves the prognosis of eyes with PVR.</jats:p> Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications Acta Ophthalmologica Scandinavica |
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10.1111/j.1600-0420.2007.00898.x |
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Acta Ophthalmologica Scandinavica |
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| title |
Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_unstemmed |
Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_full |
Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_fullStr |
Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_full_unstemmed |
Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_short |
Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_sort |
heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior pvr (hso study): design issues and implications |
| topic |
Ophthalmology |
| url |
http://dx.doi.org/10.1111/j.1600-0420.2007.00898.x |
| publishDate |
2007 |
| physical |
623-630 |
| description |
<jats:title>Abstract.</jats:title><jats:p><jats:bold>Purpose: </jats:bold> Proliferative vitreoretinopathy (PVR) is the most important reason for blindness following retinal detachment. Presently, vitreous tamponades such as gas or silicone oil cannot contact the lower part of the retina. A heavier‐than‐water tamponade displaces the inflammatory and PVR‐stimulating environment from the inferior area of the retina. The Heavy Silicone Oil versus Standard Silicone Oil Study (HSO Study) is designed to answer the question of whether a heavier‐than‐water tamponade improves the prognosis of eyes with PVR of the lower retina.</jats:p><jats:p><jats:bold>Methods: </jats:bold> The HSO Study is a multicentre, randomized, prospective controlled clinical trial comparing two endotamponades within a two‐arm parallel group design. Patients with inferiorly and posteriorly located PVR are randomized to either heavy silicone oil or standard silicone oil as a tamponading agent. Three hundred and fifty consecutive patients are recruited per group. After intraoperative re‐attachment, patients are randomized to either standard silicone oil (1000 cSt or 5000 cSt) or Densiron<jats:sup>®</jats:sup> as a tamponading agent. The main endpoint criteria are complete retinal attachment at 12 months and change of visual acuity (VA) 12 months postoperatively compared with the preoperative VA. Secondary endpoints include complete retinal attachment before endotamponade removal, quality of life analysis and the number of retina affecting re‐operation within 1 year of follow‐up.</jats:p><jats:p><jats:bold>Results: </jats:bold> The design and early recruitment phase of the study are described.</jats:p><jats:p><jats:bold>Conclusions: </jats:bold> The results of this study will uncover whether or not heavy silicone oil improves the prognosis of eyes with PVR.</jats:p> |
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| author | Joussen, Antonia M., Kirchhof, Bernd, Schrage, Norbert, Ocklenburg, Christina, Hilgers, Ralf‐Dieter |
| author_facet | Joussen, Antonia M., Kirchhof, Bernd, Schrage, Norbert, Ocklenburg, Christina, Hilgers, Ralf‐Dieter, Joussen, Antonia M., Kirchhof, Bernd, Schrage, Norbert, Ocklenburg, Christina, Hilgers, Ralf‐Dieter |
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| description | <jats:title>Abstract.</jats:title><jats:p><jats:bold>Purpose: </jats:bold> Proliferative vitreoretinopathy (PVR) is the most important reason for blindness following retinal detachment. Presently, vitreous tamponades such as gas or silicone oil cannot contact the lower part of the retina. A heavier‐than‐water tamponade displaces the inflammatory and PVR‐stimulating environment from the inferior area of the retina. The Heavy Silicone Oil versus Standard Silicone Oil Study (HSO Study) is designed to answer the question of whether a heavier‐than‐water tamponade improves the prognosis of eyes with PVR of the lower retina.</jats:p><jats:p><jats:bold>Methods: </jats:bold> The HSO Study is a multicentre, randomized, prospective controlled clinical trial comparing two endotamponades within a two‐arm parallel group design. Patients with inferiorly and posteriorly located PVR are randomized to either heavy silicone oil or standard silicone oil as a tamponading agent. Three hundred and fifty consecutive patients are recruited per group. After intraoperative re‐attachment, patients are randomized to either standard silicone oil (1000 cSt or 5000 cSt) or Densiron<jats:sup>®</jats:sup> as a tamponading agent. The main endpoint criteria are complete retinal attachment at 12 months and change of visual acuity (VA) 12 months postoperatively compared with the preoperative VA. Secondary endpoints include complete retinal attachment before endotamponade removal, quality of life analysis and the number of retina affecting re‐operation within 1 year of follow‐up.</jats:p><jats:p><jats:bold>Results: </jats:bold> The design and early recruitment phase of the study are described.</jats:p><jats:p><jats:bold>Conclusions: </jats:bold> The results of this study will uncover whether or not heavy silicone oil improves the prognosis of eyes with PVR.</jats:p> |
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| spelling | Joussen, Antonia M. Kirchhof, Bernd Schrage, Norbert Ocklenburg, Christina Hilgers, Ralf‐Dieter 1395-3907 1600-0420 Wiley Ophthalmology http://dx.doi.org/10.1111/j.1600-0420.2007.00898.x <jats:title>Abstract.</jats:title><jats:p><jats:bold>Purpose: </jats:bold> Proliferative vitreoretinopathy (PVR) is the most important reason for blindness following retinal detachment. Presently, vitreous tamponades such as gas or silicone oil cannot contact the lower part of the retina. A heavier‐than‐water tamponade displaces the inflammatory and PVR‐stimulating environment from the inferior area of the retina. The Heavy Silicone Oil versus Standard Silicone Oil Study (HSO Study) is designed to answer the question of whether a heavier‐than‐water tamponade improves the prognosis of eyes with PVR of the lower retina.</jats:p><jats:p><jats:bold>Methods: </jats:bold> The HSO Study is a multicentre, randomized, prospective controlled clinical trial comparing two endotamponades within a two‐arm parallel group design. Patients with inferiorly and posteriorly located PVR are randomized to either heavy silicone oil or standard silicone oil as a tamponading agent. Three hundred and fifty consecutive patients are recruited per group. After intraoperative re‐attachment, patients are randomized to either standard silicone oil (1000 cSt or 5000 cSt) or Densiron<jats:sup>®</jats:sup> as a tamponading agent. The main endpoint criteria are complete retinal attachment at 12 months and change of visual acuity (VA) 12 months postoperatively compared with the preoperative VA. Secondary endpoints include complete retinal attachment before endotamponade removal, quality of life analysis and the number of retina affecting re‐operation within 1 year of follow‐up.</jats:p><jats:p><jats:bold>Results: </jats:bold> The design and early recruitment phase of the study are described.</jats:p><jats:p><jats:bold>Conclusions: </jats:bold> The results of this study will uncover whether or not heavy silicone oil improves the prognosis of eyes with PVR.</jats:p> Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications Acta Ophthalmologica Scandinavica |
| spellingShingle | Joussen, Antonia M., Kirchhof, Bernd, Schrage, Norbert, Ocklenburg, Christina, Hilgers, Ralf‐Dieter, Acta Ophthalmologica Scandinavica, Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications, Ophthalmology |
| title | Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_full | Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_fullStr | Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_full_unstemmed | Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_short | Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| title_sort | heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior pvr (hso study): design issues and implications |
| title_unstemmed | Heavy silicone oil versus standard silicone oil as vitreous tamponade in inferior PVR (HSO Study): design issues and implications |
| topic | Ophthalmology |
| url | http://dx.doi.org/10.1111/j.1600-0420.2007.00898.x |