Clinical outcomes of neonatal meningitis in very-low-birth-weight infants

Citation
Ba. Doctor et al., Clinical outcomes of neonatal meningitis in very-low-birth-weight infants, CLIN PEDIAT, 40(9), 2001, pp. 473-480
Citations number
24
Categorie Soggetti
Pediatrics
Journal title
CLINICAL PEDIATRICS
ISSN journal
00099228 → ACNP
Volume
40
Issue
9
Year of publication
2001
Pages
473 - 480
Database
ISI
SICI code
0009-9228(200109)40:9<473:COONMI>2.0.ZU;2-V
Abstract
We sought to describe the clinical presentation and consequences of meningi tis among 64 very-low-birth-weight (VLBW <1.5 kg) infants who had 67 cultur e-proven episodes of meningitis over an 18-year period, 1977 through 1995. Demographic and neonatal descriptors of meningitis and later outcomes were retrospectively examined and neurodevelopmental outcomes of 39 of 45 (87%) meningitis survivors were compared to those of nonmeningitis survivors foll owed up to 20 months corrected age. Causes of meningitis included coagulase -negative Staphylococcus in 43% of episodes, other gram-positive bacteria i n 19%, gram-negative bacteria in 17%, and Candida species in 20% of episode s. Spinal fluid abnormalities were sparse, regardless of etiologic organism . Of 38 nonbloody spinal fluid taps (<1,000 erythrocytes/mm(3)), 6 had > 30 leukocytes/mm(3), 5 protein > 150 mg/dL%, and 6 glucose < 30 mg/dL (1.67 m mol/L). Only 10 infants (26%) had 1 or more of these spinal fluid abnormali ties. Meningitis survivors had a higher rate of major neurologic abnormalit y (41% vs 11%, p <0.001) and subnormal (< 70) Mental Development Index (38% vs 14%, p <0.001) than nonmeningitis survivors. Impairment rates did not d iffer by etiologic organism. The effect of meningitis on neurologic outcome persisted even after controlling for birth weight, intraventricular hemorr hage, chronic lung disease, and social risk factors (odds ratio 2.27 [95% C I 1.02, 5.05]). We conclude that despite a sparsity of abnormal spinal flui d findings, culture-proven neonatal meningitis among VLBW infants has a det rimental effect on neurologic outcome, which persists even after controllin g for other risk factors.