Italian National Blood Centre, National Institute of Health, Rome, Italy.
Department of Haematology and Transfusion Medicine, "Carlo Poma" Hospital, Mantua, Italy.
Blood Transfus. 2019 May;17(3):200-209. doi: 10.2450/2019.0080-19.
The use of blood-derived eye drops for topical treatment of ocular surface diseases has progressively increased in recent years.
To evaluate the use of serum eye drops in ocular surface disorders, we performed a systematic search of the literature.
In this systematic review, we included 19 randomised controlled trials (RCTs) investigating the use of serum eye drops in 729 patients compared to controls. For the quantitative synthesis, we included only 10 RCTs conducted in patients with dry eye syndrome comparing autologous serum to artificial tears. At 2-6 weeks, no clear between-group differences in Schirmer test (MD 1.05; 95% CI: -0.17-2.26) and in fluorescein staining (MD -0.61; 95% CI: -1.50-0.28) were found (very low-quality evidence, down-graded for inconsistency, serious risk of biases, and serious imprecision). Slightly higher increase in tear film break-up time (TBUT) scores in autologous serum compared to control (MD 2.68; 95% CI: 1.33-4.03), and greater decrease in ocular surface disease index (OSDI) in autologous serum compared to control (MD -11.17; 95% CI: -16.58 - -5.77) were found (low quality evidence, down-graded for serious risk of bias, and for inconsistency). For the Schirmer test, fluorescein staining and TBUT, data were also available at additional follow-up timing (2-12 months): no clear between-group differences were found, and the quality of the evidence was graded as low/very-low.
In patients with dry eye syndrome, it is unclear whether or not the use of autologous serum compared to artificial tears increases Schirmer test and fluorescein staining scores at short-term and medium-/long-term follow up. Some benefit at short-term follow up for the outcome of TBUT and OSDI was observed, but the quality of the evidence was low.
近年来,血液衍生的眼药水在眼部表面疾病的局部治疗中的应用逐渐增加。
为了评估血清眼药水在眼部表面疾病中的应用,我们对文献进行了系统检索。
在这项系统评价中,我们纳入了 19 项随机对照试验(RCT),共纳入 729 名患者,将血清眼药水与对照组进行比较。对于定量综合分析,我们仅纳入了 10 项在干燥性眼综合征患者中比较自体血清与人工泪液的 RCT。在 2-6 周时,在 Schirmer 测试(MD 1.05;95%CI:-0.17-2.26)和荧光素染色(MD-0.61;95%CI:-1.50-0.28)方面,两组间无明显差异(极低质量证据,因不一致性、严重偏倚风险和严重不精确性而下调)。与对照组相比,自体血清组泪膜破裂时间(TBUT)评分略有升高(MD 2.68;95%CI:1.33-4.03),且自体血清组眼表面疾病指数(OSDI)降低(MD-11.17;95%CI:-16.58- -5.77)(低质量证据,因严重偏倚风险和不一致性而下调)。对于 Schirmer 测试、荧光素染色和 TBUT,还在其他随访时间(2-12 个月)获得了数据:两组间无明显差异,证据质量被评为低/极低。
在干燥性眼综合征患者中,与人工泪液相比,自体血清是否会增加短期和中/长期随访时的 Schirmer 测试和荧光素染色评分尚不清楚。在短期随访时,TBUT 和 OSDI 的结果观察到一些益处,但证据质量较低。