Roohipoor Ramak, Karkhaneh Reza, Farahani Afsar, Ebrahimiadib Nazanin, Modjtahedi Bobeck, Fotouhi Akbar, Yaseri Mehdi, Khodabande Alireza, Zarei Mohammad, Imani Fuladi Marjan, Taheri Arash, Riazi Esfahani Mohammad, Loewenstein John
Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Retina Service, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, USA.
Arch Dis Child Fetal Neonatal Ed. 2016 Jul;101(4):F288-93. doi: 10.1136/archdischild-2015-309137. Epub 2016 Apr 12.
To test the applicability of existing retinopathy of prematurity (ROP) guidelines on Iranian patients and to develop novel ROP screening criteria in Iran.
Both eyes of 1932 infants born ≤37 weeks of gestation and/or weighting ≤3000 g were included in this prospective cohort study that was conducted across nine neonatal intensive care units and a tertiary eye hospital ROP clinic. The patients were examined for ROP and the need for treatment (type 1 ROP or worse). All the patients were screened 4 weeks after birth or at 31 weeks of postmenstrual age, whichever was later. The patients were followed until retinal vascularisation was completed or the patients reached 50 weeks of gestational age (GA) without prethreshold ROP. A receiver operating characteristic curve was used to determine the best screening criteria for ROP. Screening criteria from other countries were applied to our patient data to determine their ability to appropriately detect ROP.
Patients with ROP requiring treatment.
The mean GA±SD and birth weight (BW)±SD of the screened patients were 32±2.7 weeks and 1713±516 g, respectively. Using criteria of GA≤32 weeks or BW ≤2000 yielded sensitivity and specificity of 100% and 26.7%, respectively, for treatment requiring ROP regardless of clinical comorbidities. Using screening recommendations of American Academy of Pediatrics would miss 25.4% of ROP and 8.4%ROP requiring treatment in our cohort.
Other countries screening recommendations would result in a significant amount of missed cases of treatment requiring ROP when applied to Iran. As a result, we have proposed new guidelines for premature babies in Iran.
检验现有早产儿视网膜病变(ROP)指南对伊朗患者的适用性,并制定伊朗新的ROP筛查标准。
本前瞻性队列研究纳入了1932例孕周≤37周和/或出生体重≤3000g的婴儿,研究在9个新生儿重症监护病房和一家三级眼科医院的ROP门诊进行。对患者进行ROP检查及治疗需求(1型ROP或更严重情况)评估。所有患者在出生后4周或孕龄31周时进行筛查,以较晚者为准。对患者进行随访,直至视网膜血管化完成或患者达到孕龄50周且无阈值前ROP。采用受试者工作特征曲线确定ROP的最佳筛查标准。将其他国家的筛查标准应用于我们的患者数据,以确定其适当检测ROP的能力。
需要治疗的ROP患者。
筛查患者的平均孕龄±标准差和出生体重(BW)±标准差分别为32±2.7周和1713±516g。使用孕龄≤32周或出生体重≤2000g的标准,无论临床合并症如何,对于需要治疗的ROP,敏感性和特异性分别为100%和26.7%。采用美国儿科学会的筛查建议,在我们的队列中会漏诊25.4%的ROP和8.4%需要治疗的ROP。
应用于伊朗时,其他国家的筛查建议会导致大量需要治疗的ROP漏诊病例。因此,我们为伊朗的早产儿提出了新的指南。