Your browser doesn't support javascript.
loading
[Boston keratoprosthesis: 73 eyes from Germany : An overview of experiences from two centers]. / Boston-Keratoprothese: 73 Augen aus Deutschland : Übersicht der Erfahrungen aus zwei Zentren.
Schaub, F; Neuhann, I; Enders, P; Bachmann, B O; Koller, B; Neuhann, T; Cursiefen, C.
Afiliación
  • Schaub F; Zentrum für Augenheilkunde, Universität zu Köln, Köln, Deutschland. friederike.schaub@uk-koeln.de.
  • Neuhann I; MVZ Prof. Neuhann mit Augenabteilung, Rotkreuzklinikum München, München, Deutschland.
  • Enders P; Zentrum für Augenheilkunde, Universität zu Köln, Köln, Deutschland.
  • Bachmann BO; Zentrum für Augenheilkunde, Universität zu Köln, Köln, Deutschland.
  • Koller B; MVZ Prof. Neuhann mit Augenabteilung, Rotkreuzklinikum München, München, Deutschland.
  • Neuhann T; MVZ Prof. Neuhann mit Augenabteilung, Rotkreuzklinikum München, München, Deutschland.
  • Cursiefen C; Zentrum für Augenheilkunde, Universität zu Köln, Köln, Deutschland.
Ophthalmologe ; 115(9): 744-753, 2018 Sep.
Article en De | MEDLINE | ID: mdl-29043440
BACKGROUND: The Boston Keratoprosthesis (B-KPro) is a therapeutic option for corneal replacement for visual rehabilitation in eyes with poor a prognosis for penetrating keratoplasty (high-risk eyes). Since 2009, this approach has been used in the MVZ Prof. Neuhann, Munich, and since 2013 also at the Department of Ophthalmology, University of Cologne. An overview of results from the first 73 eyes in these departments is presented. METHODS: All recipient eyes of both centers which received a B-KPro type I (BI-KPro) between November 2009 and March 2017 were included. Indications, preoperative findings, intraoperative procedures, and clinical results, as well as postoperative complication and retention rates were documented and analyzed. RESULTS: A total of 73 eyes from 68 patients (mean age 55 ± 21.1 years, range 7 months-93 years; 26 women, 42 men) were treated with a BI-KPro. In 53 eyes (72.6%) the BI-KPro was implanted due to corneal graft failure, whereas BI-KPro was used as the primary corneal replacement in 20 eyes (27.4%). In 46 eyes (63.0%) a long-term increase in visual acuity was achieved and in 21.9% visual acuity was stabilized, while a decrease in preoperative visual acuity occurred in 15.1% of cases. During an average follow-up of 24.7 ± 23.0 months (range 1-78 months), 1.7 ± 2.4 re-interventions (range 0-9) were required. Only 4 keratoprostheses (5.5%) could not be retained. In 3 eyes (4.2%), a change of the BI-KPro device was necessary. CONCLUSION: There is a wide range of indications for BI-KPro in eyes with a poor prognosis for conventional keratoplasty. The surgical technique is safe but with a notable postoperative complication rate, which does not seem to decrease in the medium or long term. The retention rate is excellent for eyes without stem cell deficiency. Nevertheless, the BI-KPro is the only therapeutic option for high-risk eyes and leads to a gain in visual acuity in most cases.
Asunto(s)
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Órganos Artificiales / Enfermedades de la Córnea Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Europa Idioma: De Revista: Ophthalmologe Asunto de la revista: OFTALMOLOGIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Órganos Artificiales / Enfermedades de la Córnea Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Europa Idioma: De Revista: Ophthalmologe Asunto de la revista: OFTALMOLOGIA Año: 2018 Tipo del documento: Article