1977
DOI: 10.1016/s0022-3476(77)80835-4
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Toxicity to bilirubin in neonates: Infant development during first year in relation to maximum neonatal serum bilirubin concentration

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Cited by 127 publications
(38 citation statements)
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“…If the clinician does not agree with the risk-benefit profile on which the guideline is based or does not anticipate the occurrence of the adverse outcomes being addressed by the guideline, then there may be resistance to adhere to the guideline. Although some studies [21][22][23][24][25] have found associations between serum bilirubin and neurodevelopmental outcomes, none has shown any long-term beneficial effects of phototherapy. 26 -28 Thus, the primary rationale for phototherapy must be to keep the bilirubin from rising to a level at which there is an increased risk of kernicterus.…”
Section: Discussionmentioning
confidence: 99%
“…If the clinician does not agree with the risk-benefit profile on which the guideline is based or does not anticipate the occurrence of the adverse outcomes being addressed by the guideline, then there may be resistance to adhere to the guideline. Although some studies [21][22][23][24][25] have found associations between serum bilirubin and neurodevelopmental outcomes, none has shown any long-term beneficial effects of phototherapy. 26 -28 Thus, the primary rationale for phototherapy must be to keep the bilirubin from rising to a level at which there is an increased risk of kernicterus.…”
Section: Discussionmentioning
confidence: 99%
“…These risk factors include positive family history, hyperbilirubinemia, exposure to ototoxic medications, hypoxia, birth asphyxia and intracranial hemorrhages, including intraventricular hemorrhage. [2][3][4][5][6][7] The exact anatomical location of abnormality or injury and the pathophysiology of AN are poorly understood. As such, there are no specific risk factors to distinguish AN from cochlear hearing loss.…”
Section: Introductionmentioning
confidence: 99%
“…The difference in prevalence in relation to gestational age not found significant. In contrast to these, other studies like Scheidt et al (12) reported significant relationship of gestational age and neurodevelopmental abnormalities which were more in babies with low gestational age, Wolf et al reported that neurodevelopmental abnormalities were more in those hyper-bilirubinemic neonates who were having lower gestational age. (8) Prevalence of abnormal neurodevelopmental outcome in neonates having peak serum bilirubin (PSB) >25mg/dl was 37.5% and 25% in follow ups at 3 months and 12 months.…”
Section: Discussionmentioning
confidence: 74%