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Background Aluminum, a contaminant of commercial intravenous-feeding solutions, is potentially neurotoxic. We investigated the effect of perinatal exposure to intravenous aluminum on the neurologic development of infants born prematurely.
Methods We randomly assigned 227 premature infants with gestational ages of less than 34 weeks and birth weights of less than 1850 g who required intravenous feeding before they could begin enteral feeding to receive either standard or specially constituted, aluminum-depleted intravenous-feeding solutions. The neurologic development of the 182 surviving infants who could be tested was assessed by using the Bayley Scales of Infant Development at 18 months of age.
Results The 90 infants who received the standard feeding solutions had a mean (±SD) Bayley Mental Development Index of 95±22, as compared with 98±20 for the 92 infants who received the aluminum-depleted solutions (P = 0.39). In a planned subgroup analysis of infants in whom the duration of intravenous feeding exceeded the median and who did not have neuromotor impairment, the mean values for the Bayley Mental Development Index for the 39 infants who received the standard solutions and the 41 infants who received the aluminum-depleted solutions were 92±20 and 102±17, respectively (P = 0.02). The former were significantly more likely (39 percent, vs. 17 percent of the latter group; P = 0.03) to have a Mental Development Index of less than 85, increasing their risk of subsequent educational problems. For all 157 infants without neuromotor impairment, increasing aluminum exposure was associated with a reduction in the Mental Development Index (P = 0.03), with an adjusted loss of one point per day of intravenous feeding for infants receiving the standard solutions.
Conclusions In preterm infants, prolonged intravenous feeding with solutions containing aluminum is associated with impaired neurologic development.
Source Information
From the Medical Research Council (MRC) Dunn Nutrition Unit and University of Cambridge Department of Paediatrics, Cambridge (N.J.B.); the MRC Childhood Nutrition Research Centre, Institute of Child Health, London (R.M., A.L.); and the University of Manchester Department of Chemistry, Manchester (J.P.D.) all in the United Kingdom.
Address reprint requests to Dr. Bishop at the Genetics Unit, Shriners' Hospital for Crippled Children, 1529 Cedar Ave., Montreal, QC H3G 1A6, Canada.
Related Letters:
Aluminum Toxicity in Preterm Infants
Driscoll W. R., Cummings J. J., Zorn W., Bishop N. J., Morley R.
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Full Text
N Engl J Med 1997;
337:1090-1091, Oct 9, 1997.
Correspondence
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