Quality of life and functional vision in adolescents with surgically treated hydrocephalus in infancy

Abstract

AbstractAimTo evaluate health‐ and vision‐related quality of life (HR‐ and VR‐QoL) and perceptual visual dysfunction (PVD) in adolescents with hydrocephalus surgically treated in infancy.MethodsIn total, 23 adolescents (15 males and 8 females; median age 14.9 years) with hydrocephalus and 31 controls were evaluated using validated instruments to measure HR‐QoL and VR‐QoL. PVDs were reported by history taking in five areas: recognition, orientation, depth, movement and simultaneous perception.ResultsAdolescents with hydrocephalus and the parent proxy reports showed lower mean total Paediatric Quality of Life Inventory 4.0 scores (75.8 and 63.7, respectively) compared with controls (87.6 and 91.5), p = 0.016 and p < 0.0001. Parent‐reported scores were lower than self‐reported scores (p = 0.001). Adolescents with myelomeningocele (n = 10) showed lower physical health scores (p = 0.001). No VR‐QoL difference was found between groups. PVDs were reported in ≥1 area by 14/23 hydrocephalus participants and 2/31 controls (p < 0.0001). Associations were found in the hydrocephalus group between VR‐QoL and HR‐QoL (rs = 0.47, p = 0.026) and number of PVD areas (rs = −0.6, p = 0.003).ConclusionAdolescents with hydrocephalus and their parents reported lower HR‐QoL and more PVDs. These problems indicate the need for not only ophthalmological follow‐ups but also evaluation of QoL and PVDs in individuals with infantile hydrocephalus.