Suppr超能文献

在不同的新生儿群体中,未结合胆红素可预测异常的自动听性脑干反应。

Unbound bilirubin predicts abnormal automated auditory brainstem response in a diverse newborn population.

作者信息

Ahlfors C E, Amin S B, Parker A E

机构信息

Division of Neonatology, Department of Pediatrics, California Pacific Medical Center, San Francisco, CA, USA.

出版信息

J Perinatol. 2009 Apr;29(4):305-9. doi: 10.1038/jp.2008.199. Epub 2009 Feb 26.

Abstract

OBJECTIVE

The objective of this study was to determine if plasma unbound or 'free' bilirubin concentration (B(f)) measured during the first 30 days of life is associated with subsequent abnormal hearing screening testing by automated auditory brainstem response (AABR) in a diverse population of newborns.

STUDY DESIGN

An observational study of newborns receiving AABR, plasma total bilirubin concentration (TBC) and B(f) measurements and without underlying conditions known to affect hearing was conducted. Logistic regression was used to determine associations between abnormal AABR and B(f) or TBC. The impacts of a variety of clinical factors on the regression model were also assessed.

RESULT

A total of 191 patients with birth weights and gestations ranging from 406 to 4727 g and 24 to 42 weeks, respectively, were studied. Among them, 175 (92%) had normal (bilateral PASS) AABR and 16 had abnormal AABR (6 had unilateral REFER AABR, and 10 had bilateral REFER AABR). Mean TBC was not significantly different in babies with normal or abnormal AABR, but mean B(f) was greater in the latter group (1.76 versus 0.93 microg per 100 ml, respectively, P=0.012). B(f), but not TBC, was associated with an abnormal AABR (B(f) adjusted odds ratio 3.3, 95% CI 1.8 to 6.1). Comparing receiver-operating characteristics curves, the B(f)/TBC ratio was a better predictor of an abnormal AABR than B(f) alone. Intraventricular hemorrhage was the only confounding clinical variable.

CONCLUSION

An abnormal AABR is associated with an elevated B(f) or B(f)/TBC ratio, but not the TBC alone. The prevalence of bilirubin neurotoxicity as a cause of audiological dysfunction may be underestimated if the TBC alone is used to assess the severity of newborn jaundice.

摘要

目的

本研究的目的是确定在出生后30天内测量的血浆未结合或“游离”胆红素浓度(B(f))是否与不同人群新生儿随后通过自动听性脑干反应(AABR)进行的异常听力筛查测试相关。

研究设计

对接受AABR、血浆总胆红素浓度(TBC)和B(f)测量且无已知影响听力的潜在疾病的新生儿进行了一项观察性研究。采用逻辑回归来确定异常AABR与B(f)或TBC之间的关联。还评估了各种临床因素对回归模型的影响。

结果

共研究了191例出生体重在406至4727克之间、孕周在24至42周之间的患者。其中,175例(92%)AABR正常(双侧通过),16例AABR异常(6例单侧未通过AABR,10例双侧未通过AABR)。正常或异常AABR的婴儿平均TBC无显著差异,但后一组的平均B(f)更高(分别为每100毫升1.76微克和0.93微克,P = 0.012)。与异常AABR相关的是B(f)而非TBC(B(f)调整后的优势比为3.3,95%可信区间为1.8至6.1)。比较接受者操作特征曲线,B(f)/TBC比值比单独的B(f)更能预测异常AABR。脑室内出血是唯一的混杂临床变量。

结论

异常AABR与升高的B(f)或B(f)/TBC比值相关,但与单独的TBC无关。如果仅使用TBC来评估新生儿黄疸的严重程度,胆红素神经毒性作为听力功能障碍原因的患病率可能被低估。

相似文献

1
Unbound bilirubin predicts abnormal automated auditory brainstem response in a diverse newborn population.
J Perinatol. 2009 Apr;29(4):305-9. doi: 10.1038/jp.2008.199. Epub 2009 Feb 26.
2
Performance of two hearing screening protocols in NICU in Shanghai.
Int J Pediatr Otorhinolaryngol. 2011 Oct;75(10):1225-9. doi: 10.1016/j.ijporl.2011.07.004. Epub 2011 Jul 28.
3
Short- and long-term outcome of severe neonatal nonhemolytic hyperbilirubinemia.
J Child Neurol. 2006 Apr;21(4):309-15. doi: 10.1177/08830738060210040301.
5
Auditory neuropathy in late preterm infants treated with phototherapy for hyperbilirubinemia.
Int J Audiol. 2015 Feb;54(2):89-95. doi: 10.3109/14992027.2014.938779. Epub 2014 Aug 26.
6
Efficacy of automated auditory brainstem response hearing screening in very preterm newborns.
J Pediatr. 2001 May;138(5):674-8. doi: 10.1067/mpd.2001.112646.
8
Bilirubin and serial auditory brainstem responses in premature infants.
Pediatrics. 2001 Apr;107(4):664-70. doi: 10.1542/peds.107.4.664.
9
The outcomes of an audiological management programme for neonates with hyperbilirubinaemia.
S Afr J Commun Disord. 2024 Oct 9;71(1):e1-e6. doi: 10.4102/sajcd.v71i1.1014.

引用本文的文献

1
The Effect of Intravenous Albumin Administration Before Exchange Transfusion in Infants With Hyperbilirubinemia: A Meta-Analysis.
Health Sci Rep. 2025 Jul 27;8(8):e71079. doi: 10.1002/hsr2.71079. eCollection 2025 Aug.
2
Factors Affecting the Relationship Between Total and Unbound Bilirubin in Preterm and Term Infants.
Acta Paediatr. 2025 Aug;114(8):1977-1981. doi: 10.1111/apa.70067. Epub 2025 Mar 22.
5
175 Years of Bilirubin Testing: Ready for Point-of-Care?
Adv Healthc Mater. 2023 Jul;12(18):e2203380. doi: 10.1002/adhm.202203380. Epub 2023 Apr 10.
8
Crigler-Najjar Syndrome Type 1: Pathophysiology, Natural History, and Therapeutic Frontier.
Hepatology. 2020 Jun;71(6):1923-1939. doi: 10.1002/hep.30959. Epub 2020 Feb 5.
9
High unbound bilirubin for age: a neurotoxin with major effects on the developing brain.
Pediatr Res. 2019 Jan;85(2):183-190. doi: 10.1038/s41390-018-0224-4. Epub 2018 Dec 5.
10
Developmental influence of unconjugated hyperbilirubinemia and neurobehavioral disorders.
Pediatr Res. 2019 Jan;85(2):191-197. doi: 10.1038/s41390-018-0216-4. Epub 2018 Oct 23.

本文引用的文献

2
Effects of sample dilution, peroxidase concentration, and chloride ion on the measurement of unbound bilirubin in premature newborns.
Clin Biochem. 2007 Feb;40(3-4):261-7. doi: 10.1016/j.clinbiochem.2006.09.006. Epub 2006 Sep 29.
3
Outcomes among newborns with total serum bilirubin levels of 25 mg per deciliter or more.
N Engl J Med. 2006 May 4;354(18):1889-900. doi: 10.1056/NEJMoa054244.
5
Clinical assessment of bilirubin-induced neurotoxicity in premature infants.
Semin Perinatol. 2004 Oct;28(5):340-7. doi: 10.1053/j.semperi.2004.09.005.
7
An evidence-based review of important issues concerning neonatal hyperbilirubinemia.
Pediatrics. 2004 Jul;114(1):e130-53. doi: 10.1542/peds.114.1.e130.
9
Unbound bilirubin in a term newborn with kernicterus.
Pediatrics. 2003 May;111(5 Pt 1):1110-2. doi: 10.1542/peds.111.5.1110.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验