# Utility of Clinical, Laboratory, and Radiological Parameters for Detecting Hypovolemia in Edematous Children With Steroid-Sensitive Nephrotic Syndrome—A Prospective Observational Study

**Authors:** N. V. Shikha, C. Krishnan, P. K. Aslam, Gomathy Subramaniam, M. P. Jayakrishnan

PMC · DOI: 10.1155/ijpe/5040795 · International Journal of Pediatrics · 2025-11-05

## TL;DR

This study found that one-third of children with a kidney condition called nephrotic syndrome had low blood volume, and certain clinical signs can help identify it.

## Contribution

The study evaluates the effectiveness of clinical and radiological markers in detecting hypovolemia in children with nephrotic syndrome.

## Key findings

- High hematocrit was the most sensitive marker for hypovolemia, with 80% sensitivity.
- IVCCI ≥ 50% showed the highest specificity (91.6%) for detecting hypovolemia.
- Half of the children with hypovolemia were symptomatic.

## Abstract

A prospective observational study was conducted in 90 edematous children with steroid-sensitive nephrotic syndrome (SSNS) to determine the prevalence of hypovolemia and also to study the role of surrogate markers like severe edema, high hematocrit, inferior vena cava collapsibility index (IVCCI) ≥ 50%, blood urea/creatinine ≥ 100 : 1, and serum albumin < 1.5 gm/dL in identifying hypovolemia. The diagnostic test for hypovolemia was a combination of FeNa < 0.5 and urinary potassium (UK) index ≥ 0.6. One-third of children with SSNS had hypovolemia, of which 50% were symptomatic. High hematocrit was the most sensitive surrogate marker of hypovolemia (80%), followed by serum albumin < 1.5 g/dL (56.6%), IVCCI ≥ 50% (43%), severe edema (36.7%), and blood urea/creatinine ≥ 100 : 1 (33.3%). The specificity for detecting hypovolemia was maximum for IVCCI ≥ 50% (91.6%), followed by blood urea/creatinine ≥ 100 : 1 (90%), serum albumin < 1.5 g/dL (85%), severe edema (81.7%), and hemoconcentration (21.6%).

## Linked entities

- **Diseases:** nephrotic syndrome (MONDO:0005377)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** Hypovolemia (MESH:D020896), Edematous (MESH:D004487), Nephrotic Syndrome (MESH:D009404)
- **Chemicals:** urea (MESH:D014508), Steroid (MESH:D013256), potassium (MESH:D011188), creatinine (MESH:D003404), FeNa (-)

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12611466/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12611466/full.md

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Source: https://tomesphere.com/paper/PMC12611466