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已发表模型用于减轻早产儿视网膜病变筛查负担的验证

Validation of a Published Model to Reduce Burden of Retinopathy of Prematurity Screening.

作者信息

Pruett Jaron, Ruland Kelly, Donahue Sean

机构信息

From the Vanderbilt University School of Medicine (J.P.) Nashville, Tennessee, USA.

Vanderbilt Eye Institute Department of Pediatric Ophthalmology (K.R.), Nashville, Tennessee, USA.

出版信息

Am J Ophthalmol. 2024 Jan;257:12-15. doi: 10.1016/j.ajo.2023.09.004. Epub 2023 Sep 9.

Abstract

PURPOSE

The E-ROP study evaluated 1257 patients screened for retinopathy of prematurity (ROP), and found that no infant born at or after 27 weeks' gestational age and having a birthweight over 750 g developed treatable disease if they had no ROP at 37 weeks' gestational age. The study investigators suggested that there is little value in continued screening of infants meeting these criteria who have no ROP at 37 weeks. We attempted to replicate these published data in a larger multi-center cohort to validate or refute this hypothesis.

DESIGN

Retrospective cohort study.

METHODS

We conducted a chart review of every infant treated for ROP from February 2004 through April 2022 at 6 medical centers located in the mid-southern region of the United States. We evaluated gestational age, birthweight, and presence or absence of ROP at 37 weeks' gestational age to determine whether any treated infants would have been "missed" using these screening criteria.

RESULTS

Of 6729 infants screened, 298 (4.43%) received treatment. Ten infants who required treatment developed first evidence of ROP after 37 weeks' gestational age. However, only 1 infant was >750 g birthweight and >27 weeks' gestational age. This patient developed zone 2, stage 3 with pre-plus disease and was treated because of limited access to care at a remote hospital; however, ROP was detected at the first examination after 37 weeks, so this infant would have been identified for continued follow-up.

CONCLUSION

Our results, in a cohort 5 times that of the original study, replicated that infants >750 g birthweight and >27 weeks' gestational age did not develop treatable ROP if they had no ROP at 37 weeks, supporting the termination of examination at that time in patients meeting these criteria.

摘要

目的

“早期ROP研究”评估了1257例接受早产儿视网膜病变(ROP)筛查的患者,发现孕龄27周及以后出生且出生体重超过750克的婴儿,如果在孕37周时没有ROP,则不会发展为可治疗的疾病。该研究的调查人员认为,对于符合这些标准且在37周时没有ROP的婴儿,继续进行筛查几乎没有价值。我们试图在一个更大的多中心队列中重复这些已发表的数据,以验证或反驳这一假设。

设计

回顾性队列研究。

方法

我们对2004年2月至2022年4月期间在美国中南部地区的6个医疗中心接受ROP治疗的每例婴儿的病历进行了回顾。我们评估了孕龄、出生体重以及孕37周时是否存在ROP,以确定使用这些筛查标准是否会“遗漏”任何接受治疗的婴儿。

结果

在6729例接受筛查的婴儿中,298例(4.43%)接受了治疗。10例需要治疗的婴儿在孕37周后首次出现ROP迹象。然而,只有1例婴儿出生体重>750克且孕龄>27周。该患者发展为2区3期伴有加前期疾病,因在偏远医院难以获得医疗服务而接受治疗;然而,ROP在37周后的首次检查中被发现,因此该婴儿本应被确定继续随访。

结论

我们的研究结果来自一个比原研究大5倍的队列,重复了出生体重>750克且孕龄>27周的婴儿如果在37周时没有ROP则不会发展为可治疗的ROP的结果,支持对符合这些标准的患者在那时终止检查。

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