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Multicenter Study
. 2012 Dec 28:12:198.
doi: 10.1186/1471-2431-12-198.

Outcome at two years of age in a Swiss national cohort of extremely preterm infants born between 2000 and 2008

Collaborators, Affiliations
Multicenter Study

Outcome at two years of age in a Swiss national cohort of extremely preterm infants born between 2000 and 2008

Luregn J Schlapbach et al. BMC Pediatr. .

Abstract

Background: While survival rates of extremely preterm infants have improved over the last decades, the incidence of neurodevelopmental disability (ND) in survivors remains high. Representative current data on the severity of disability and of risk factors associated with poor outcome in this growing population are necessary for clinical guidance and parent counselling.

Methods: Prospective longitudinal multicentre cohort study of preterm infants born in Switzerland between 24(0/7) and 27(6/7) weeks gestational age during 2000-2008. Mortality, adverse outcome (death or severe ND) at two years, and predictors for poor outcome were analysed using multilevel multivariate logistic regression. Neurodevelopment was assessed using Bayley Scales of Infant Development II. Cerebral palsy was graded after the Gross Motor Function Classification System.

Results: Of 1266 live born infants, 422 (33%) died. Follow-up information was available for 684 (81%) survivors: 440 (64%) showed favourable outcome, 166 (24%) moderate ND, and 78 (11%) severe ND. At birth, lower gestational age, intrauterine growth restriction and absence of antenatal corticosteroids were associated with mortality and adverse outcome (p < 0.001). At 36(0/7) weeks postmenstrual age, bronchopulmonary dysplasia, major brain injury and retinopathy of prematurity were the main predictors for adverse outcome (p < 0.05). Survival without moderate or severe ND increased from 27% to 39% during the observation period (p = 0.02).

Conclusions: In this recent Swiss national cohort study of extremely preterm infants, neonatal mortality was determined by gestational age, birth weight, and antenatal corticosteroids while neurodevelopmental outcome was determined by the major neonatal morbidities. We observed an increase of survival without moderate or severe disability.

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Figures

Figure 1
Figure 1
Changes in mortality and in frequency of severe and moderate neurodevelopmental disability during the study period. FU, follow-up; ND, neurodevelopmental disability.
Figure 2
Figure 2
Spline figures showing non-linear associations of gestational age and birth weight with mortality (A, B) and with adverse outcome (C, D). The birth weight z-score (A, C) and the gestational age in weeks (B, D) are given on the X-axis. Each mark on the X-axis represents a patient. In panel B and D the duration of gestational age was rounded to one decimal. The natural logarithm of the multivariate Odd’s ratio for the respective outcome is shown (y-axis and solid line) with the 95%-confidence intervals (dashed lines).
Figure 3
Figure 3
Model of prediction of outcome according to count of four risk factors (bronchopulmonary dysplasia, major brain injury, retinopathy of prematurity stage 3 or higher, and necrotizing enterocolitis and/or proven sepsis). The proportion of adverse outcome (A) and of favourable outcome (B) with 95%-confidence intervals and the number of infants per group are shown. The dotted horizontal line indicates the average proportion of the respective outcome. The dashed diagonal line represents the regression line. ND, neurodevelopmental disability. The figure shows data from 670 children because information on risk factor ROP (stage 3 or higher) was not available in 14 of 684 patients.

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