Abstract
Detecting overhydration in children on chronic ambulatory peritoneal dialysis (CAPD) is critical as it contributes to cardiovascular morbidity and mortality. However, precise clinical assessment of overhydration is challenging. Bio-impedance vector analysis (BIVA) is a bedside body composition tool that can estimate overhydration with a potential role of guiding the clinician on fluid management. This study aimed to longitudinally assess and compare the overhydration status detected using clinical assessment and BIVA in children on CAPD. A longitudinal observational study was undertaken in clinically stable children (age 4-18years) on CAPD (minimum duration of 6 months) from May 2017 to January 2020 at the pediatric chronic kidney disease clinic of a tertiary hospital. Presence of overhydration was assessed by clinical signs, bioimpedance measures and BIVA at enrollment, 3 and 6 months of follow up. Modifications to CAPD prescriptions and antihypertensive medications were based only on clinical assessment. Children were categorized as having clinical overhydration if they fulfilled 2 of 3 criteria of weight gain (>7% of body weight), uncontrolled hypertension (office BP ≥95thcentiles despite being on anti-hypertensive medications) and presence of signs of fluid overload. Based on a normative reference R-Xc graph, derived from z-scores of 20 healthy controls, bioimpedance vectors were plotted. The position of the vector in the left lower quadrant beyond the 95% tolerance ellipse was regarded as overhydration. Differences in the longitudinal vector displacement were analyzed using Hotelling’s T2 test. Twenty six children [18 boys, median age 9.5(4,16)years] on CAPD for 21(12,72) months were enrolled. Non-glomerular etiology was noted in 69% and 58% had residual kidney function. At enrollment, the proportion of children with overhydration assessed clinically and by BIVA was 34.6% and 30.7% respectively. There was poor agreement between measures of overhydration by clinical assessment and BIVA at all three time points. Among those detected to be overhydrated at enrollment, 9/11 (82%) and 4/9 (44%) remained overhydrated at 6 months by BIVA and clinical assessment respectively. The BIVA plots on the reference RXc graph (Figure) revealed a significant difference in the vector displacement towards the quadrant of overhydration at all time points, with the maximum difference seen between enrollment and 6 months (T2 = 32.58, p <0.001). In children on CAPD, there is poor agreement between measures of overhydration detected clinically and by BIVA. Longitudinal vector plots over 6 months reflect persistence of overhydration in a majority, as compared to clinical assessment. Further studies to explore the utility of BIVA in guiding the clinician with fluid management in these children are warranted.
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