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Plasma rich in growth factors membrane as coadjuvant treatment in the surgery of ocular surface disorders

机译:血浆富含生长因子膜作为眼表疾病手术的辅助治疗

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To evaluate the safety and efficacy of the surgical use of plasma rich in growth factors fibrin membrane (mPRGF) in different ocular surface pathologies. Fifteen patients with different corneal and conjunctival diseases were included in the study. Patients were grouped according to the use of mPRGF as graft (corneal and/or conjunctival) or dressing; they were also grouped according to the surgical subgroup of intervention (persistent corneal ulcer [PCU], keratoplasty, superficial keratectomy, corneal perforation, and pterygium). Best corrected visual acuity, intraocular pressure (IOP), inflammation control time (ICT), mPRGF AT ( PRGF membrane absorption time), and the healing time of the epithelial defect (HTED) were evaluated throughout the clinical follow-up time. Safety assessment was also performed reporting all adverse events. mPRGF showed a total closure of the defect in 13 of 15 patients (86.7%) and a partial closure in 2 patients (13.3%). The mean follow-up time was 11.1 ± 4.2 (4.8–22.8) months, the mean ICT was 2.5 ± 1.1 (1.0–4.0) months, the mean mPRGF AT was 12.4 ± 2.0 (10.0–16.0) days, and for the global HTED the mean was 2.9 ± 1.2 (1–4.8) months. Results showed an improvement in BCVA in all patients, with an overall improvement of 2.9 in Vision Lines. The BCVA significantly improved ( P .05) throughout the clinical follow-up time. No adverse events were reported after mPRGF use. The mPRGF is effective and safe as coadjuvant treatment in surgeries related with ocular surface disorders, being an alternative to the use of amniotic membrane. The mPRGF accelerates tissue regeneration after ocular surface surgery thus minimizing inflammation and fibrosis.
机译:为了评估在不同的眼表病理情况下手术使用富含生长因子纤维蛋白膜(mPRGF)血浆的安全性和有效性。本研究纳入了15名不同角膜和结膜疾病的患者。根据mPRGF作为移植物(角膜和/或结膜)或敷料的使用将患者分组。他们还根据外科手术干预分组(持续性角膜溃疡[PCU],角膜移植术,浅表角膜切除术,角膜穿孔和翼状g肉)。在整个临床随访期间,评估最佳矫正视力,眼内压(IOP),炎症控制时间(ICT),mPRGF AT(PRGF膜吸收时间)和上皮缺损的愈合时间(HTED)。还进行了安全评估,报告了所有不良事件。 mPRGF在15例患者中有13例完全闭合缺损(86.7%),在2例患者中部分闭合(13.3%)。平均随访时间为11.1±4.2(4.8–22.8)个月,平均ICT为2.5±1.1(1.0–4.0)个月,平均mPRGF AT为12.4±2.0(10.0–16.0)天, HTED平均为2.9±1.2(1-4.8)个月。结果表明,所有患者的BCVA均有改善,而Vision Lines的总体改善为2.9。在整个临床随访期间,BCVA显着改善(P = 0.05)。使用mPRGF后未报告不良事件。在与眼表疾病有关的手术中,mPRGF作为辅助治疗是有效和安全的,是羊膜使用的替代方法。 mPRGF加速了眼表手术后的组织再生,从而最大程度地减少了炎症和纤维化。

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