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Randomized Controlled Trial
. 2006 Mar;32(3):396-406.
doi: 10.1016/j.jcrs.2006.02.014.

ESCRS study of prophylaxis of postoperative endophthalmitis after cataract surgery: Case for a European multicenter study

Affiliations
Randomized Controlled Trial

ESCRS study of prophylaxis of postoperative endophthalmitis after cataract surgery: Case for a European multicenter study

David V Seal et al. J Cataract Refract Surg. 2006 Mar.

Erratum in

  • J Cataract Refract Surg. 2006 May;32(5):709

Abstract

Purpose: To present the development and design of the European Society of Cataract & Refractive Surgeons multicenter study of the prevention of postsurgical infective endophthalmitis after phacoemulsification and to describe the process for its successful implementation and conduct.

Setting: Twenty-four ophthalmology units and eye clinics in Austria, Belgium, Germany, Italy, Poland, Portugal, Spain, Turkey, and the United Kingdom, with an administrative office in Ireland, coordinating center in England, and data management and statistical unit in Scotland.

Methods: This partially masked randomized placebo-controlled multinational clinical study was designed to evaluate prospectively the prophylactic effect of intracameral cefuroxime and/or perioperative topical levofloxacin on postoperative endophthalmitis after cataract surgery. Random allocation was based on a 2 x 2 factorial design that included participating centers as a class variable. Real-time electronic data collection monitored study progress and provided weekly outcome tables, monthly recruitment summaries, and quarterly analytical reports for the study's Data Monitoring Committee, which evaluated the safety and efficacy by Internet-based conferences.

Results: A 2-year lead time was required to meet harmonized standards of clinical research in the European Union, obtain ministerial authorization in 3 countries, gain institutional approvals at 24 hospitals, and procure indemnity insurance for surgical centers. Informed consent instruments, designed to comply with national health policies, were translated into 8 languages. The use of information technology to collect study data enabled the organizers to evaluate individual eligibility at enrollment, adherence with study medications during and after surgery, and postoperative status during follow-up.

Conclusion: This international cooperative study provided the opportunity to estimate the current incidence of endophthalmitis after cataract surgery in Europe and determine whether 1 or both of 2 antimicrobial regimens reduces the risk for postsurgical intraocular infection.

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Comment in

  • Prophylaxis of postoperative endophthalmitis.
    Spokes DM, Walters G. Spokes DM, et al. J Cataract Refract Surg. 2007 Apr;33(4):561; author reply 561. doi: 10.1016/j.jcrs.2006.11.022. J Cataract Refract Surg. 2007. PMID: 17397710 No abstract available.

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