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Published on: September 25, 2017
Potential implications of subclinical hypervolemia, identified by a multiparametric approach, in causing left
Marco Allinovi1,2, Valentina Querin3, Silvia Menale4
1Nephrology, Dialysis and Transplantation Unit, Careggi University Hospital, Florence, Italy. marco.allinovi@gmail.com.
Insights
Subclinical hypervolemia in children on dialysis, identified using lung ultrasound (LUS), bioimpedance spectroscopy (BIS), and inferior vena cava collapsibility index (IVC-CI), is linked to left ventricular hypertrophy (LVH). This multiparametric approach aids in early detection and risk assessment for cardiac complications.
Area of Science:
- Pediatric Nephrology
- Cardiovascular Physiology
- Diagnostic Imaging
Background:
- Fluid overload in pediatric dialysis patients can cause serious cardiac issues like left ventricular hypertrophy (LVH) and dysfunction.
- Persistent subclinical hypervolemia, appearing as euvolemia clinically but hypervolemia technically, lacks thorough investigation for its cardiovascular impact.
- This pilot study addresses the gap by exploring methods to detect subclinical hypervolemia and its cardiac effects in children undergoing dialysis.
Purpose of the Study:
- To evaluate the combined utility of lung ultrasound (LUS), bioimpedance spectroscopy (BIS), and inferior vena cava collapsibility index (IVC-CI) in identifying subclinical hypervolemia in children on chronic dialysis.
- To investigate the association between subclinical hypervolemia and cardiac complications, specifically left ventricular hypertrophy (LVH).
Main Methods:
- A longitudinal study involving 23 children on chronic dialysis.
- Regular fluid status assessments every 2 months using physical examination, LUS, IVC-CI, and BIS.
- Echocardiography performed every 6 months to assess cardiac parameters.
Main Results:
- Significant correlations were found between interdialytic weight gain and LUS B-lines (R=0.2923, p<0.001) and BIS OH/ECW (R=0.4144, p<0.001) in clinically euvolemic patients.
- A negative correlation was observed between interdialytic weight gain and IVC-CI (R=-0.2597, p=0.019).
- Subclinical hypervolemia was associated with a higher incidence of hypertensive crises (67% vs. 0%, p<0.01) and LVH (75% vs. 27%, p=0.04).
Conclusions:
- The multiparametric approach combining LUS, BIS, and IVC-CI effectively quantifies subclinical hypervolemia in clinically euvolemic children on dialysis.
- Subclinical hypervolemia identified through this method is significantly correlated with an increased risk of developing left ventricular hypertrophy (LVH).
Background:
Fluid overload in children undergoing dialysis can lead to serious cardiac complications, i.e., left ventricular hypertrophy (LVH) and cardiac dysfunction. Studies investigating the cardiovascular effects of persistent subclinical hypervolemia-characterized by euvolemia at clinical assessment but hypervolemia at technical evaluation-are lacking. This pilot study explored the combined use of lung ultrasound (LUS), bioimpedance spectroscopy (BIS), and ultrasound assessment of the inferior vena cava collapsibility index (IVC-CI) to identify subclinical hypervolemia and investigated its cardiac impact.
Methods:
In this longitudinal study, we recruited 23 children on chronic dialysis who underwent fluid status evaluation (physical examination, LUS, IVC-CI, BIS) every 2 months and echocardiography every 6 months.
Results:
In clinically euvolemic patients, we observed a significant positive correlation between the interdialytic weight gain and the number of B-lines observed by LUS (R = 0.2923, p < 0.001); similar results were obtained for the OH/ECW measured by BIS (R = 0.4144, p < 0.001), while a negative correlation with IVC-CI (R = - 0.2597, p = 0.019) was observed. Moreover, we identified a significant linear correlation between left ventricular mass index values and the average pre-dialysis systolic blood pressure measured over the preceding 6 months (R2 = 0.16, p = 0.002). Hospitalizations due to hypertensive crises (67% vs. 0%, p < 0.01) and the occurrence of LVH at the final follow-up (75% vs. 27%, p = 0.04) were notably more frequent in children with subclinical hypervolemia.
Conclusion:
In clinically euvolemic children on dialysis, the combined use of LUS, BIS, and IVC-CI (multiparametric approach) effectively quantified subclinical hypervolemia, which was correlated with the risk of LVH.
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