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波士顿 1 型角膜假体的中远期疗效的系统评价和荟萃分析。

Systematic Review and Meta-Analysis of the Medium- and Long-Term Outcomes of the Boston Type 1 Keratoprosthesis.

机构信息

Brighton & Sussex Medical School, Brighton, United Kingdom.

Sussex Eye Hospital, Brighton and Sussex University Hospitals NHS Trust, Brighton, United Kingdom.

出版信息

Cornea. 2019 Nov;38(11):1465-1473. doi: 10.1097/ICO.0000000000002098.

DOI:10.1097/ICO.0000000000002098
PMID:31403526
Abstract

PURPOSE

The Boston type 1 keratoprosthesis (KPro), used in patients with high risk of corneal graft failure, is increasingly being used. However, the medium- to long-term outcomes are currently unclear. We analyzed the medium- (2-5 years) and long-term (>5 years) efficacy and safety of the Boston type 1 KPro in terms of visual outcomes, device retention, and postoperative complications.

METHODS

We last searched electronic databases (Ovid MEDLINE, Ovid MEDLINE In-Process and Other Non-Indexed Citations, Ovid MEDLINE Daily, Ovid MEDLINE Epub Ahead of Print, EMBASE, and CENTRAL) on March 31, 2018. Visual outcomes and device retention at 2 and 5 years, alongside postoperative complications, were primary outcome measures.

RESULTS

We identified 407 articles. Thirty studies were included in this systematic review and meta-analysis. The combined proportion of eyes with ≥6/60 vision was 62% at 2 years and 51% at 5 years. The combined retention rate was 88% at 2 years and 74% at 5 years. Retroprosthetic membrane (36.6%) and glaucoma (39.3%) were found to be the most common long-term complications. Very few studies showed visual outcomes or retention rates at 5 years, with results sparse and collectively not meaningful because of small patient numbers and ambiguous reporting of follow-up times.

CONCLUSIONS

The 2-year results indicate that there is a place for the Boston type 1 KPro in the management of corneal blindness. However, there is scarce evidence regarding its medium- and long-term efficacy and safety. The high rate of reported complications necessitates strict patient selection and stringent follow-up.

摘要

目的

波士顿 1 型角膜假体(KPro)用于高角膜移植失败风险的患者,其应用越来越广泛。然而,目前尚不清楚其中期(2-5 年)和长期(>5 年)的疗效和安全性。我们分析了波士顿 1 型 KPro 的中期(2-5 年)和长期(>5 年)的疗效和安全性,包括视力结果、器械保留率和术后并发症。

方法

我们最后一次检索电子数据库(Ovid MEDLINE、Ovid MEDLINE In-Process 和其他非索引引文、Ovid MEDLINE Daily、Ovid MEDLINE Epub Ahead of Print、EMBASE 和 CENTRAL)的时间为 2018 年 3 月 31 日。2 年和 5 年时的视力结果和器械保留率以及术后并发症是主要的观察指标。

结果

我们共检索到 407 篇文章,其中 30 篇研究纳入了本系统综述和荟萃分析。2 年时,≥6/60 视力的眼睛比例合并为 62%,5 年时为 51%。2 年时的合并保留率为 88%,5 年时为 74%。术后发生的最常见的长期并发症是后弹力层膜(36.6%)和青光眼(39.3%)。只有少数研究报告了 5 年时的视力结果或保留率,由于患者数量较少且随访时间报告不明确,结果稀疏且总体上无意义。

结论

2 年的结果表明,波士顿 1 型 KPro 在角膜盲的治疗中有一定的地位。然而,目前关于其中期和长期疗效和安全性的证据有限。报告的并发症发生率较高,需要严格的患者选择和严格的随访。

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