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

被引:66
作者
Ahlfors, C. E. [1 ]
Amin, S. B. [2 ]
Parker, A. E. [1 ]
机构
[1] Calif Pacific Med Ctr, Div Neonatol, Dept Pediat, San Francisco, CA USA
[2] Univ Rochester, Sch Med, Dept Pediat, Div Neonatol, Rochester, NY 14642 USA
关键词
hyperbilirubinemia; unbound bilirubin; automated auditory brainstem response; BIRTH-WEIGHT INFANTS; PREMATURE-INFANTS; HEARING-LOSS; NEONATAL HYPERBILIRUBINEMIA; EXCHANGE-TRANSFUSION; JAUNDICED NEWBORNS; SERUM BILIRUBIN; KERNICTERUS; OUTCOMES;
D O I
10.1038/jp.2008.199
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
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 Bf 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 mu g per 100 ml, respectively, P = 0.012). Bf, 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.
引用
收藏
页码:305 / 309
页数:5
相关论文
共 24 条
[1]
AHLFORS CE, 1994, PEDIATRICS, V93, P488
[2]
Unbound bilirubin in a term newborn with kernicterus [J].
Ahlfors, CE ;
Herbsman, O .
PEDIATRICS, 2003, 111 (05) :1110-1112
[3]
Unbound bilirubin concentration is associated with abnormal automated auditory brainstem response for jaundiced newborns [J].
Ahlfors, Charles E. ;
Parker, Anne E. .
PEDIATRICS, 2008, 121 (05) :976-978
[4]
Effects of sample dilution, peroxidase concentration, and chloride ion on the measurement of unbound bilirubin in premature newborns [J].
Ahlfors, Charles E. ;
Vreman, Hendrik J. ;
Wong, Ronald J. ;
Bender, G. Jesse ;
Oh, William ;
Morris, Brenda H. ;
Stevenson, David K. .
CLINICAL BIOCHEMISTRY, 2007, 40 (3-4) :261-267
[5]
Clinical assessment of bilirubin-induced neurotoxicity in premature infants [J].
Amin, SB .
SEMINARS IN PERINATOLOGY, 2004, 28 (05) :340-347
[6]
Bilirubin and serial auditory brainstem responses in premature infants [J].
Amin, SB ;
Ahlfors, C ;
Orlando, MS ;
Dalzell, LE ;
Merle, KS ;
Guillet, R .
PEDIATRICS, 2001, 107 (04) :664-670
[7]
Newborn hearing screening in the NICU: Profile of failed auditory brainstem response/passed otoacoustic emission [J].
Berg, AL ;
Spitzer, JB ;
Towers, HM ;
Bartosiewicz, C ;
Diamond, BE .
PEDIATRICS, 2005, 116 (04) :933-938
[8]
CAUSE OF HEARING-LOSS IN THE HIGH-RISK PREMATURE-INFANT [J].
BERGMAN, I ;
HIRSCH, RP ;
FRIA, TJ ;
SHAPIRO, SM ;
HOLZMAN, I ;
PAINTER, MJ .
JOURNAL OF PEDIATRICS, 1985, 106 (01) :95-101
[9]
CASHORE WJ, 1982, PEDIATRICS, V69, P481
[10]
COCHLEAR AND BRAIN-STEM RESPONSES IN HEARING-LOSS FOLLOWING NEONATAL HYPER-BILITRUBINEMIA [J].
CHISIN, R ;
PERLMAN, M ;
SOHMER, H .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1979, 88 (03) :352-357