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Uterine Fibroid Embolization (UFE) with optisphere: A prospective study of a new, spherical, resorbable embolic agent

Uterine Fibroid Embolization (UFE) with optisphere: A prospective study of a new, spherical, resorbable embolic agent
Uterine Fibroid Embolization (UFE) with optisphere: A prospective study of a new, spherical, resorbable embolic agent

INTRODUCTION: Optisphere (Teleflex, Wayne, PA, USA, currently distributed by Medtronic, Minneapolis, MN, USA) is a new, resorbable, calibrated spherical embolic agent. We aimed to evaluate its clinical safety and effectiveness for fibroid embolization through a prospective case series.

METHOD: This prospective case series studied patients treated with fibroid embolization using Optisphere between July 2017 and June 2018. The primary outcomes were device-related adverse event assessments and MRI-determined percentage infarct of the dominant fibroid (DF %) and infarct of all fibroids (AF %) at 3 months post-embolization. Secondary outcomes included symptom improvement with the validated Uterine Fibroid Symptom Score and Quality of Life questionnaire (UFS-SS and UFS-QOL) at 3 months and 12 months post-embolization. Statistical analysis was through the Wilcoxon signed-rank test for nonparametric paired data.

RESULTS: Twenty-three consecutive patients were treated with Optisphere (median age 44.0, uterine volume 484.0 ml, dominant fibroid volume 167.0 ml). The complete dominant fibroid infarction (DF %) rate was 91.3% (21/23 patients), and the complete all fibroid infarction rate (AF %) was 82.6% (19/23). No adverse device-related safety events were encountered. Significant improvement was demonstrated in 3-month UFS-SS (56 vs 19, p < 0.0001), UFS-QOL (40 vs 88, p = 0.0008), uterine volume (484 ml vs 246 ml, p < 0.0001) and dominant fibroid volume (167 vs 64 ml, p < 0.0001). Symptomatic improvement continued to 12 months (UFS-SS 56 vs 11, p = 0.0008, UFS-QOL 40 vs 98.7, p = 0.0008).

CONCLUSION: Optisphere is an effective embolic agent for fibroid embolization with good symptomatic response and percentage fibroid infarct.

Adult, Embolization, Therapeutic/instrumentation, Female, Humans, Leiomyoma/therapy, Prospective Studies, Quality of Life, Surveys and Questionnaires, Treatment Outcome, Uterine Neoplasms/therapy
0174-1551
897-903
Hacking, Nigel
fdc70f9c-e9d6-485c-a53d-e6988fa75cb0
Maclean, Drew
bf15fb9d-aa6d-4d13-8cae-ede6a3329779
Vigneswaran, Ganesh
4e3865ad-1a15-4a27-b810-55348e7baceb
Bryant, Timothy
05bd12ef-e864-450e-96f5-addcc60c173d
Modi, Sachin
caef086a-dda5-418a-ada8-fc042e6e0b18
Hacking, Nigel
fdc70f9c-e9d6-485c-a53d-e6988fa75cb0
Maclean, Drew
bf15fb9d-aa6d-4d13-8cae-ede6a3329779
Vigneswaran, Ganesh
4e3865ad-1a15-4a27-b810-55348e7baceb
Bryant, Timothy
05bd12ef-e864-450e-96f5-addcc60c173d
Modi, Sachin
caef086a-dda5-418a-ada8-fc042e6e0b18

Hacking, Nigel, Maclean, Drew, Vigneswaran, Ganesh, Bryant, Timothy and Modi, Sachin (2020) Uterine Fibroid Embolization (UFE) with optisphere: A prospective study of a new, spherical, resorbable embolic agent. Cardiovascular and Interventional Radiology, 43 (6), 897-903. (doi:10.1007/s00270-020-02460-2).

Record type: Article

Abstract

INTRODUCTION: Optisphere (Teleflex, Wayne, PA, USA, currently distributed by Medtronic, Minneapolis, MN, USA) is a new, resorbable, calibrated spherical embolic agent. We aimed to evaluate its clinical safety and effectiveness for fibroid embolization through a prospective case series.

METHOD: This prospective case series studied patients treated with fibroid embolization using Optisphere between July 2017 and June 2018. The primary outcomes were device-related adverse event assessments and MRI-determined percentage infarct of the dominant fibroid (DF %) and infarct of all fibroids (AF %) at 3 months post-embolization. Secondary outcomes included symptom improvement with the validated Uterine Fibroid Symptom Score and Quality of Life questionnaire (UFS-SS and UFS-QOL) at 3 months and 12 months post-embolization. Statistical analysis was through the Wilcoxon signed-rank test for nonparametric paired data.

RESULTS: Twenty-three consecutive patients were treated with Optisphere (median age 44.0, uterine volume 484.0 ml, dominant fibroid volume 167.0 ml). The complete dominant fibroid infarction (DF %) rate was 91.3% (21/23 patients), and the complete all fibroid infarction rate (AF %) was 82.6% (19/23). No adverse device-related safety events were encountered. Significant improvement was demonstrated in 3-month UFS-SS (56 vs 19, p < 0.0001), UFS-QOL (40 vs 88, p = 0.0008), uterine volume (484 ml vs 246 ml, p < 0.0001) and dominant fibroid volume (167 vs 64 ml, p < 0.0001). Symptomatic improvement continued to 12 months (UFS-SS 56 vs 11, p = 0.0008, UFS-QOL 40 vs 98.7, p = 0.0008).

CONCLUSION: Optisphere is an effective embolic agent for fibroid embolization with good symptomatic response and percentage fibroid infarct.

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More information

Published date: 31 March 2020
Keywords: Adult, Embolization, Therapeutic/instrumentation, Female, Humans, Leiomyoma/therapy, Prospective Studies, Quality of Life, Surveys and Questionnaires, Treatment Outcome, Uterine Neoplasms/therapy

Identifiers

Local EPrints ID: 448622
URI: http://eprints.soton.ac.uk/id/eprint/448622
ISSN: 0174-1551
PURE UUID: 027dbb25-cc0e-4cbd-812a-c2cec22d03d3
ORCID for Ganesh Vigneswaran: ORCID iD orcid.org/0000-0002-4115-428X

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Date deposited: 28 Apr 2021 16:32
Last modified: 17 Mar 2024 04:06

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Contributors

Author: Nigel Hacking
Author: Drew Maclean
Author: Timothy Bryant
Author: Sachin Modi

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