尼日利亚哈科特港早产儿视网膜病变。

ISRN ophthalmology Pub Date : 2014-02-04 eCollection Date: 2014-01-01 DOI:10.1155/2014/481527
Adedayo O Adio, Rosemary O Ugwu, Chidi G Nwokocha, Augusta U Eneh
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引用次数: 28

摘要

目的。由于尼日利亚新生儿护理的改善,许多早产儿得以存活,但早产儿视网膜病变(ROP)导致的视力损害/失明的发生率可能会上升。我们在一个15岁的特殊护理婴儿病房首次开始筛查后描述了我们的发现,以确定发生ROP的发病率和危险因素。方法。一项前瞻性研究于2012年1月1日至10月31日在哈科特港大学教学医院的特殊护理婴儿部(SCBU)和儿科门诊进行。在知情同意的情况下,53名早产儿(550名在研究期间入院的新生儿)在32周内出生,体重小于1500 g被纳入研究,主要结局指标是ROP的任何阶段的发展。结果。平均胎龄28.98±1.38周。平均出生体重1411±128 g。在SCBU接收的550名婴儿中,100名早产儿中有87名存活,其中53名被纳入研究。25例(47.2%)存在不同程度的ROP,患病率为47.2%。体重过重的婴儿患病率更高(75%)
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Retinopathy of prematurity in port harcourt, Nigeria.

Retinopathy of prematurity in port harcourt, Nigeria.

Purpose. With many preterm babies now surviving as a result of improvement in neonatal care in Nigeria, the incidence of visual impairment/blindness as a result of retinopathy of prematurity (ROP) may rise. We describe our findings after screening starts for the first time in a 15-year-old special care baby unit so as to establish the incidence and risk factors for developing ROP. Methods. A prospective study carried out at the Special Care Baby Unit (SCBU) and Pediatric Outpatient Clinics of the University of Port Harcourt Teaching Hospital between January 1 and October 31, 2012. Fifty-three preterm babies (of 550 neonates admitted within the study period) delivered before 32 completed weeks and weighing less than 1500 g were included in the study following informed consent and the main outcome measure was the development of any stage of ROP. Results. Mean gestational age at birth was 28.98 ± 1.38 weeks. Mean birth weight was 1411 ± 128 g. Out of 550 babies admitted at SCBU, 87 of 100 preterms survived with 53 included in study. Twenty-five (47.2%) had different degrees of ROP with prevalence found to be 47.2%. Prevalence was higher (75%) in babies weighing <1300 g and those delivered before 30-week gestation (58%). Twenty-one (84%) had stage 1 no plus disease and 3 (12%) had stage 2 no plus disease. Only 1 (4%) had threshold disease in Zone 1. None had disease at stage 4 or 5 or AP-ROP. Receiving supplemental oxygen (χ (2) = 6.17; P = 0.01), presence of sepsis (χ (2) = 7.47; P = 0.006), multiple blood transfusions (χ (2) = 5.11; P = 0.02), and delivery by caesarian section (χ (2) = 4.22; P = 0.04) were significantly associated with development of ROP. There were no significant differences with gender, apneic spells, jaundice, or phototherapy. Conclusions and Relevance. All live infants with ROP were noted to regress spontaneously in this study. Though it may not be cost effective to acquire treatment facilities at the moment (the only child with treatable disease died), facilities for screening preterm infants displaying high risk features may be essential as smaller babies are saved.

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