{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T20:24:48Z","timestamp":1777580688607,"version":"3.51.4"},"reference-count":24,"publisher":"SAGE Publications","issue":"5","license":[{"start":{"date-parts":[[2020,9,29]],"date-time":"2020-09-29T00:00:00Z","timestamp":1601337600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"funder":[{"name":"PhysiolIOL SA"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["European Journal of Ophthalmology"],"published-print":{"date-parts":[[2021,9]]},"abstract":"<jats:sec>\n                    <jats:title>Purpose:<\/jats:title>\n                    <jats:p>To determine the visual outcome, intraocular lens (IOL) stability and posterior capsule opacification (PCO) rate of a hydrophobic acrylic intraocular lens.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Setting:<\/jats:title>\n                    <jats:p>Vienna Institute for Research in Ocular Surgery, Hanusch Hospital, Vienna, Austria<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design:<\/jats:title>\n                    <jats:p>This double-masked randomised study included patients who underwent standard cataract surgery.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Method:<\/jats:title>\n                    <jats:p>Patients received either the hydrophobic acrylic IOL (iPure, PhysIOL) or the hydrophobic acrylic control IOL (Tecnis ZCB00, Johnson&amp;Johnson). Subjective refraction, uncorrected and corrected distance visual acuity (UDVA, CDVA), IOL tilt and decentration (Purkinje meter) and PCO intensity using retroillumination images with automated image analysis (automated quantification of after-cataract, AQUA), were evaluated for both groups 2\u2009years after surgery.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>A total number of 31 patients completed the 2-year follow-up, 16 in the study group and 15 in the control group. The CDVA was 0.0 logMAR (standard deviation \u2013 SD: 0.1) for the study IOL and 0.1 logMAR (SD: 0.2) for the control IOL, p\u2009=\u20090.001. The AQUA PCO score for the study group was 2.1 and 1.4 for the control group, p\u2009=\u20090.44. Mean IOL tilt was 2.9\u00b0 (SD: 1.8) in the study group and 5.0\u00b0 (SD: 4.5) in the control group, whilst the mean decentration was 0.37\u2009mm (SD: 0.18) and 0.45\u2009mm (SD: 0.3), p\u2009=\u20090.610.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>The studied parameters revealed a good performance for both IOLs. Both IOLs had good CDVA, a small amount of tilt and decentration and none of the patients required laser capsulotomies during the follow-up time of 2\u2009years after surgery. Presented at the 37th ESCRS Congress Paris, France, September 2019<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/1120672120960591","type":"journal-article","created":{"date-parts":[[2020,9,30]],"date-time":"2020-09-30T02:01:06Z","timestamp":1601431266000},"page":"2377-2382","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Capsular bag performance of a novel hydrophobic acrylic single-piece intraocular lens: Two-year results of a randomised controlled trial"],"prefix":"10.1177","volume":"31","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4246-6389","authenticated-orcid":false,"given":"Andreea D","family":"Fi\u0219u\u0219","sequence":"first","affiliation":[{"name":"Department of Ophthalmology, Vienna Institute for Research in Ocular Surgery \u2013 Karl Landsteiner Institute, Hanusch Hospital, Vienna, Austria"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nino 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