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首页> 外文期刊>South African Journal of Child Health >An evaluation of the screening for retinopathy of prematurity in very-low-birth-weight babies at a tertiary hospital in Johannesburg, South Africa
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An evaluation of the screening for retinopathy of prematurity in very-low-birth-weight babies at a tertiary hospital in Johannesburg, South Africa

机译:在南非约翰内斯堡一家三级医院对极低出生体重的婴儿进行早产儿视网膜病变筛查的评估

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Background. Retinopathy of prematurity (ROP) is a leading cause of blindness for very-low-birth-weight (VLBW, &1 ? 500 g) babies. ROP screening identifies babies that require treatment to prevent major visual impairment. Objectives. To evaluate the screening for ROP at Charlotte Maxeke Johannesburg Academic Hospital (CMJAH) by reviewing the number of babies screened according to the CMJAH guidelines, the grades of ROP found and the treatment modality received.? Methods. This was a retrospective record review of VLBW babies born between 1 January 2013 and 31 December 2013 at CMJAH, whether inborn or transferred in. The babies were divided into two groups based on age at final outcome. Final outcome was defined as death, discharge or transfer out of the unit. The ‘early’ outcome group had their final outcome before day 28 of life. The ‘late’ outcome group had their final outcome at day 28 or more of life. The early outcome group qualified for outpatient ROP screening and the late outcome group qualified for inpatient ROP screening. Results. There were a total of 572 VLBW babies at CMJAH during this time period. The babies had a mean birth weight of 1 ? 127 (standard deviation (SD) 244.75) g and gestational age of 29 (2.743) weeks. The mean duration of stay was 29 (21.66) days and there were 309 female babies. Of these 572 babies, 304 comprised the early outcome group and 268 comprised the late outcome group. In the early outcome group babies who were transferred out of the unit or died were excluded; therefore the remaining 147 babies discharged home qualified for outpatient ROP screening. Inpatient ROP screening was carried out in 36/147 (24.4%) of these babies (not in accordance with ROP screening guidelines). ROP was documented in 4/36 (11.1%). Outpatient ROP screening records were unavailable. Exclusions from the late outcome group included five babies. In the late outcome group 111/263 (42.2%) were screened for ROP. ROP was found in 17%. One baby required treatment with intravitreal antivascular endothelial growth factor (VEGF) and three babies required surgery. ? Conclusions. More than half of the babies in the late outcome group were not screened during their stay (57.8%). More than one-third of babies were discharged prior to reaching the current recommended age for screening. Efforts need to be intensified to identify and screen all eligible babies prior to discharge. Outpatient ROP screening is not well documented; therefore prevalence cannot be established.
机译:背景。早产儿视网膜病变(ROP)是极低出生体重(VLBW,<1-500 g)婴儿失明的主要原因。 ROP筛查可确定需要治疗以防止严重视力障碍的婴儿。目标。为了评估夏洛特·马克斯·约翰内斯堡学术医院(CMJAH)的ROP筛查,方法是根据CMJAH指南检查筛查的婴儿数,发现的ROP等级和接受的治疗方式。方法。这是一项回顾性记录回顾,回顾了2013年1月1日至2013年12月31日在CMJAH出生的VLBW婴儿,无论是出生还是转入。根据最终结局,将婴儿分为两组。最终结果定义为死亡,出院或从单位转移出去。 “早期”结果组在生命的第28天之前获得了最终结果。 “晚期”结果组在生命的第28天或更长的时间里获得了最终结果。早期结果组符合门诊ROP筛查的条件,晚期结果组符合住院ROP筛查的条件。结果。在此期间,CMJAH共有572名VLBW婴儿。婴儿的平均出生体重为1? 127(标准差(SD)244.75)g,胎龄为29(2.743)周。平均住院时间为29(21.66)天,有309名女婴。在这572个婴儿中,有304个属于早期结果组,有268个属于晚期结果组。在早期结果组中,排除了被转移出单位或死亡的婴儿。因此,其余147名出院的婴儿有资格进行门诊ROP筛查。在这些婴儿中有36/147(24.4%)进行了住院ROP筛查(不符合ROP筛查指南)。 ROP的记录为4/36(11.1%)。没有门诊ROP筛查记录。结局较晚的组排除了五个婴儿。在晚期结局组中,对ROP筛查了111/263组(42.2%)。发现ROP的比例为17%。一名婴儿需要接受玻璃体内抗血管内皮生长因子(VEGF)治疗,三名婴儿需要接受手术。 ?结论。晚期结局组中超过一半的婴儿在入住期间未接受筛查(57.8%)。超过三分之一的婴儿在达到当前建议的筛查年龄之前已出院。需要加强努力,以便在出院前对所有合格的婴儿进行识别和筛查。门诊ROP筛查没有充分记录;因此无法确定患病率。

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