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INTRAVITREAL INJECTION OF PERFLUOROPROPANE IS MORE EFFICACIOUS THAN SULFUR HEXAFLUORIDE IN RELEASING VITREOMACULAR TRACTION

SUMMARY – The aim was to compare the efficacy of a single intravitreal injection of perfluoropropane (C3F8) and sulfur hexafluoride (SF6) in releasing vitreomacular traction (VMT). This prospective study included two groups of patients with symptomatic VMT confirmed by spectral-domain optical cohere...

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Autores principales: Čokl, Neža, Globočnik Petrovič, Mojca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sestre Milosrdnice University Hospital and Institute of Clinical Medical Research, Vinogradska cesta c. 29 Zagreb 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532010/
https://www.ncbi.nlm.nih.gov/pubmed/30431727
http://dx.doi.org/10.20471/acc.2018.57.02.14
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author Čokl, Neža
Globočnik Petrovič, Mojca
author_facet Čokl, Neža
Globočnik Petrovič, Mojca
author_sort Čokl, Neža
collection PubMed
description SUMMARY – The aim was to compare the efficacy of a single intravitreal injection of perfluoropropane (C3F8) and sulfur hexafluoride (SF6) in releasing vitreomacular traction (VMT). This prospective study included two groups of patients with symptomatic VMT confirmed by spectral-domain optical coherence tomography (SD-OCT). Patients from both groups received a single intravitreal injection of expansile gas. One group (29 eyes) received 0.3 mL of 100% C3F8, and the other group (28 eyes) received 0.3 mL of 100% SF6. Eyes without VMT release one month after SF6 injection were secondarily injected with C3F8. The primary outcome was the ratio of eyes in each group with complete VMT release on OCT one month following primary treatment. The secondary outcome was the ratio of reinjected eyes with complete VMT release on OCT one month following second injection. Additional outcome was the ratio of VMT release in eyes with specific clinical characteristics. One month after the application, complete release of VMT on OCT was recorded in 18 out of 29 eyes (62%) in the C3F8 group, in 6 out of 28 eyes (21.4%) in the SF6 group, and in 7 out of 14 (50%) reinjected eyes. There was no statistically significant difference in age, width of vitreomacular attachment (WVMAT), central retinal thickness and presence of additional features between the two groups. In eyes with WVMAT <500 microns, there was no statistically significant difference between the two gases in releasing VMT. In eyes with WVMAT >500 microns, C3F8 was more efficacious (p=0.001). According to the results of our study, intravitreal C3F8 injection seems to be more efficacious in releasing VMT than SF6 in eyes with WVMAT larger than 500 microns.
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spelling pubmed-65320102019-06-04 INTRAVITREAL INJECTION OF PERFLUOROPROPANE IS MORE EFFICACIOUS THAN SULFUR HEXAFLUORIDE IN RELEASING VITREOMACULAR TRACTION Čokl, Neža Globočnik Petrovič, Mojca Acta Clin Croat Original Scientific Paper SUMMARY – The aim was to compare the efficacy of a single intravitreal injection of perfluoropropane (C3F8) and sulfur hexafluoride (SF6) in releasing vitreomacular traction (VMT). This prospective study included two groups of patients with symptomatic VMT confirmed by spectral-domain optical coherence tomography (SD-OCT). Patients from both groups received a single intravitreal injection of expansile gas. One group (29 eyes) received 0.3 mL of 100% C3F8, and the other group (28 eyes) received 0.3 mL of 100% SF6. Eyes without VMT release one month after SF6 injection were secondarily injected with C3F8. The primary outcome was the ratio of eyes in each group with complete VMT release on OCT one month following primary treatment. The secondary outcome was the ratio of reinjected eyes with complete VMT release on OCT one month following second injection. Additional outcome was the ratio of VMT release in eyes with specific clinical characteristics. One month after the application, complete release of VMT on OCT was recorded in 18 out of 29 eyes (62%) in the C3F8 group, in 6 out of 28 eyes (21.4%) in the SF6 group, and in 7 out of 14 (50%) reinjected eyes. There was no statistically significant difference in age, width of vitreomacular attachment (WVMAT), central retinal thickness and presence of additional features between the two groups. In eyes with WVMAT <500 microns, there was no statistically significant difference between the two gases in releasing VMT. In eyes with WVMAT >500 microns, C3F8 was more efficacious (p=0.001). According to the results of our study, intravitreal C3F8 injection seems to be more efficacious in releasing VMT than SF6 in eyes with WVMAT larger than 500 microns. Sestre Milosrdnice University Hospital and Institute of Clinical Medical Research, Vinogradska cesta c. 29 Zagreb 2018-06 /pmc/articles/PMC6532010/ /pubmed/30431727 http://dx.doi.org/10.20471/acc.2018.57.02.14 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND) 4.0 License.
spellingShingle Original Scientific Paper
Čokl, Neža
Globočnik Petrovič, Mojca
INTRAVITREAL INJECTION OF PERFLUOROPROPANE IS MORE EFFICACIOUS THAN SULFUR HEXAFLUORIDE IN RELEASING VITREOMACULAR TRACTION
title INTRAVITREAL INJECTION OF PERFLUOROPROPANE IS MORE EFFICACIOUS THAN SULFUR HEXAFLUORIDE IN RELEASING VITREOMACULAR TRACTION
title_full INTRAVITREAL INJECTION OF PERFLUOROPROPANE IS MORE EFFICACIOUS THAN SULFUR HEXAFLUORIDE IN RELEASING VITREOMACULAR TRACTION
title_fullStr INTRAVITREAL INJECTION OF PERFLUOROPROPANE IS MORE EFFICACIOUS THAN SULFUR HEXAFLUORIDE IN RELEASING VITREOMACULAR TRACTION
title_full_unstemmed INTRAVITREAL INJECTION OF PERFLUOROPROPANE IS MORE EFFICACIOUS THAN SULFUR HEXAFLUORIDE IN RELEASING VITREOMACULAR TRACTION
title_short INTRAVITREAL INJECTION OF PERFLUOROPROPANE IS MORE EFFICACIOUS THAN SULFUR HEXAFLUORIDE IN RELEASING VITREOMACULAR TRACTION
title_sort intravitreal injection of perfluoropropane is more efficacious than sulfur hexafluoride in releasing vitreomacular traction
topic Original Scientific Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532010/
https://www.ncbi.nlm.nih.gov/pubmed/30431727
http://dx.doi.org/10.20471/acc.2018.57.02.14
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