The Effect of Immunologically Safe Plasma Rich in Growth Factor Eye Drops in Patients with Sjogren Syndrome

被引:42
|
作者
Mauricio Sanchez-Avila, Ronald [1 ]
Merayo-Lloves, Jesus [1 ]
Cristina Riestra, Ana [1 ]
Anitua, Eduardo [2 ,3 ]
Muruzabal, Francisco [2 ,3 ]
Orive, Gorka [3 ,4 ,5 ]
Fernandez-Vega, Luis [1 ]
机构
[1] Univ Oviedo, Inst Univ Fernandez Vega, Fdn Invest Oftalmol, Oviedo, Spain
[2] Fdn Eduardo Anitua, Jacinto Quincoces 39, Vitoria 01007, Spain
[3] Biotechnol Inst BTI, Vitoria, Spain
[4] Univ Basque Country, Sch Pharm, NanoBioCel Grp, Lab Pharmaceut, Vitoria, Spain
[5] Biomed Res Networking Ctr Bioengn Biomat & Nanome, Vitoria, Spain
关键词
Sjogren syndrome; plasma rich in growth factors; dry eye; PRP; platelet-rich plasma; OCULAR SURFACE DISORDERS; DRY EYE; AUTOLOGOUS SERUM; KERATOCONJUNCTIVITIS SICCA; CYCLOSPORINE-A; EFFICACY; DISEASE; CLASSIFICATION; PROLIFERATION; STIMULATION;
D O I
10.1089/jop.2016.0166
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: The objective was to provide preliminary information about the efficacy and safety of immunologically safe plasma rich in growth factor (immunosafe PRGF) eye drops in the treatment of moderate to severe dry eye in patients with primary and secondary Sjogren's syndrome (SS) and to analyze the influence of several variables on treatment outcomes. Methods: This retrospective study included patients with SS. All patients were treated with previously immunosafe PRGF eye drops to reduce the immunologic component contents. Ocular Surface Disease Index (OSDI) scale, best-corrected visual acuity (BCVA), visual analog scale (VAS) frequency, and VAS severity outcome measures were evaluated before and after treatment with immunosafe PRGF. The potential influence of some patient clinical variables on results was also assessed. Safety assessment was also performed reporting all adverse events. Results: Twenty-six patients (12 patients with primary SS, and 14 patients suffering secondary SS) with a total of 52 affected eyes were included and evaluated. Immunosafe PRGF treatment showed a significant reduction (P<0.05) in OSDI scale (41.86%), in BCVA (62.97%), in VAS frequency (34.75%), and in VAS severity (41.50%). BCVA and VAS frequency scores improved significantly (P<0.05) after concomitant treatment of PRGF with corticosteroids. Only 2 adverse events were reported in 2 patients (7.7% of patients). Conclusions: Signs and symptoms of dry eye syndrome in patients with SS were reduced after treatment with PRGF-Endoret eye drops. Immunosafe PRGF-Endoret is safe and effective for treating patients with primary and secondary SS.
引用
收藏
页码:391 / 399
页数:9
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