Sepsis is commonly experienced by infants born very preterm (<32 weeks gestational age and/or <1500 g birthweight), but the long-term functional outcomes are unclear. The objective of this systematic review was to identify observational studies comparing neurodevelopmental outcomes in very preterm infants who had blood culture-proven neonatal sepsis with those without sepsis. Twenty-four studies were identified, of which 19 used prespecified definitions of neurodevelopmental impairment and five reported neurodevelopmental outcomes as continuous variables. Meta-analysis was conducted using 14 studies with defined neurodevelopmental impairment and demonstrated that very preterm infants with neonatal sepsis were at higher risk of impairments, such as cerebral palsy and neurosensory deficits, compared with infants without sepsis (OR 3.18; 95% CI 2.29-4.41). Substantial heterogeneity existed across the studies (I 2 = 83.1, 95% CI 73-89). The five studies that reported outcomes as continuous variables showed no significant difference in cognitive performance between sepsis and non-sepsis groups. Neonatal sepsis in very preterm infants is associated with increased risk of neurodevelopmental disability. Due to the paucity of longitudinal follow-up data beyond 36 months, the long-term cognitive effect of neonatal sepsis in very preterm infants could not be conclusively determined. Effects on the development of minor impairment could not be assessed, due to the small numbers of infants included in the studies.Children 2019, 6, 131 2 of 25 proportional to gestational age, with 33% of infants born less than 28 weeks acquiring sepsis compared with 60% of infants born less than 25 weeks [5].During the neonatal period, complications such as sepsis can have dramatic effects on the growth and development of the child, especially in children born very prematurely [6,7]. The mechanism of how sepsis inflicts brain damage has been hypothesised. Research suggests the developing brain is vulnerable to the systematic inflammatory milieu characteristic of sepsis, as well as cytotoxic and ischaemic injury from hypotension and reduced cerebral blood flow [7]. Together, these factors may result in white matter abnormalities and diffuse injury to premyelinating oligodendrocytes, which have been shown to be closely associated with increased risk for impaired cognitive and motor functioning [8,9]. Such morbidities are complex and can range from major impairments, such as cerebral palsy, to more subtle deficits such as difficulties with memory and attention. Regardless, they all have the potential to affect a child's academic, social and emotional functioning. Neurodevelopmental follow-up in VP infants with sepsis is crucial for the early identification of developmental delay so that targeted interventions can be prescribed to minimise long-lasting impairments.The short-term cognitive impact of sepsis in VP infants has been studied. A systematic review of 17 studies on VLBW infants with neonatal sepsis concluded these infants are at twice the r...