Eyesight to the Blind-Pharmacotherapy for Retinopathy of Prematurity.

IF 0.6 Q4 NURSING
Christopher McPherson
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引用次数: 0

Abstract

Retinopathy of prematurity (ROP) places preterm infants at significant risk for blindness. Angiogenesis of retinal blood vessels relies on vascular endothelial growth factor (VEGF) released in response to physiologic in utero hypoxia. Relative hyperoxia and disruption in the supply of growth factors after preterm birth lead to cessation of normal vascular growth. Recovery of VEGF production after 32 weeks' postmenstrual age results in aberrant vascular growth, including the formation of fibrous scars with the potential to detach the retina. Ablation of aberrant vessels by mechanical or pharmacologic methods relies on timely diagnosis in the early stages of ROP. Mydriatic medications dilate the pupil to allow examination of the retina. Mydriasis is typically accomplished using a combination of topical phenylephrine, a potent alpha-receptor agonist, and cyclopentolate, an anticholinergic. Systemic absorption of these agents results in a high incidence of cardiovascular, gastrointestinal, and respiratory adverse effects. Procedural analgesia should include the topical anesthetic proparacaine, oral sucrose, and nonpharmacologic interventions like non-nutritive sucking. Analgesia is often incomplete, leading to investigation of systemic agents like oral acetaminophen. If ROP threatens retinal detachment, laser photocoagulation is utilized to arrest vascular growth. More recently, the VEGF-antagonists, bevacizumab and ranibizumab, have emerged as treatment options. Systemic absorption of intraocular bevacizumab and the profound consequences of diffuse disruption of VEGF in the setting of rapid, neonatal organogenesis require dose optimization and careful evaluation of long-term outcomes in clinical trials. Intraocular ranibizumab is likely a safer alternative; however, outstanding questions remain regarding efficacy. Optimal patient outcomes rely on a combination of risk management throughout neonatal intensive care, timely diagnosis through careful ophthalmologic examinations, and treatment when indicated with laser therapy and/or anti-VEGF intravitreal injection.

视力对早产儿视网膜病变的盲药治疗。
早产儿视网膜病变(ROP)使早产儿有很大的失明风险。视网膜血管的新生依赖于子宫内生理性缺氧时血管内皮生长因子(VEGF)的释放。相对高氧和早产后生长因子供应中断导致正常血管生长停止。月经后32周恢复VEGF生成导致血管异常生长,包括形成纤维疤痕,有可能使视网膜脱离。机械或药物方法消融异常血管依赖于ROP早期的及时诊断。瞳孔药物使瞳孔扩大,以便检查视网膜。抽虫病通常采用局部联合使用苯肾上腺素(一种有效的α受体激动剂)和环戊酸盐(一种抗胆碱能剂)来完成。这些药物的全身吸收导致心血管、胃肠道和呼吸道不良反应的高发。手术镇痛应包括表面麻醉剂丙帕卡因、口服蔗糖和非药物干预,如非营养性吸吮。镇痛往往是不完全的,导致研究全身性药物如口服对乙酰氨基酚。如果ROP威胁到视网膜脱离,则使用激光光凝来阻止血管生长。最近,vegf拮抗剂贝伐单抗和雷尼单抗已成为治疗选择。在快速新生儿器官发生的情况下,眼内贝伐单抗的全身吸收和血管内皮生长因子弥漫性破坏的深远影响需要在临床试验中优化剂量和仔细评估长期结果。眼内雷尼单抗可能是一种更安全的选择;然而,关于疗效,仍有悬而未决的问题。患者的最佳预后依赖于新生儿重症监护期间的风险管理,通过仔细的眼科检查及时诊断,以及在需要时进行激光治疗和/或玻璃体内注射抗vegf。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neonatal Network
Neonatal Network NURSING-
CiteScore
0.90
自引率
14.30%
发文量
87
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