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晶状体后纤维增生症。一所机构二十多年的经验。

Retrolental fibroplasia. Experience over two decades in one institution.

作者信息

Kalina R E, Karr D J

出版信息

Ophthalmology. 1982 Feb;89(2):91-5, 103. doi: 10.1016/s0161-6420(82)34829-0.

Abstract

We examined 1,849 consecutively admitted premature infants weighing 2000 gm or less at birth for retrolental fibroplasia (RLF). Proliferative RLF was diagnosed frequently in low birth weight infants who were more likely to survive with modern neonatal intensive care. Cicatricial RLF was more likely to result from proliferative RLF and to be more severe in lower birth weight infants, but most affected eyes retained useful vision. Comparison of cases diagnosed over the 20 years of this study suggest that cicatricial RLF in recent years is less likely to result in severe visual disability. Improving survival rates for lower birth weight infants mandate continued surveillance for RLF and study of improved oxygen monitoring techniques.

摘要

我们对1849名出生时体重2000克或更低的连续入院早产儿进行了晶状体后纤维增生症(RLF)检查。增生性RLF在低出生体重儿中经常被诊断出来,这些婴儿在现代新生儿重症监护下更有可能存活。瘢痕性RLF更有可能由增生性RLF引起,并且在低出生体重儿中更严重,但大多数受影响的眼睛仍保留有用视力。对本研究20年期间诊断的病例进行比较表明,近年来瘢痕性RLF导致严重视力残疾的可能性较小。提高低出生体重儿的存活率要求持续监测RLF并研究改进的氧气监测技术。

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