# Clinical efficacy of a thermosensitive embolic agent for the treatment of pediatric renal vascular hypertension due to renal artery branch stenosis in children

**Authors:** Yakun Wang, Xingmiao Liu, Ji Cheng, Dong Li, Yang Liu

PMC · DOI: 10.3389/fped.2025.1638141 · Frontiers in Pediatrics · 2025-10-16

## TL;DR

A thermosensitive embolic agent effectively treats pediatric kidney-related high blood pressure by improving symptoms, blood pressure, and organ damage.

## Contribution

This study demonstrates the clinical efficacy of thermosensitive embolic agents for treating pediatric renal vascular hypertension.

## Key findings

- Thermosensitive embolic agents significantly reduced headache severity and blood pressure in children with renal artery stenosis.
- The cure rate increased from 55.6% at 3 months to 77.8% at 6–12 months post-treatment.
- Target organ damage improved, with echocardiographic and renal function markers returning to normal levels.

## Abstract

To evaluate the clinical efficacy of a thermosensitive embolic agent in the treatment of renal vascular hypertension caused by stenosis in the renal artery branches.

We retrospectively analyzed 18 pediatric patients who were admitted to our hospital between March 2020 and January 2024 for interventional embolization due to hypertension caused by stenosis of renal artery branches. We compared the degree of headache relief, blood pressure, cure rate, improvement rate, changes in target organ damage, and renin levels before and after the treatment.

(1) Clinical symptoms significantly improved, with a marked relief of headache and significant reduction in NRS-11 scores (p < 0.05). (2) Blood pressure control showed obvious improvement, with both systolic and diastolic pressures significantly lower than pre-intervention levels (p < 0.05), and the use of antihypertensive medications were reduced (p < 0.05). (3) At the 3-month follow-up, the cure and improvement rates were 55.6% (10/18) and 44.4% (8/18), respectively. At 6–12 months, the cure rate increased to 77.8% (14/18), while the improvement rate showed a corresponding decrease to 22.2% (4/18). (4) Improvement in target organ damage: At the 3-month post-intervention follow-up, echocardiographic findings of all children had returned to normal, with no signs of left ventricular hypertrophy. Both serum creatinine(Scr) and blood urea nitrogen(BUN) levels also returned to normal. Additionally, the 24 h urinary protein quantification at 3 months post-intervention was significantly lower than pre-intervention levels. During the 6–12 month follow-up period, except for one child with a mild abnormality, urinary protein indicators of all other children remained at normal levels. (5) Changes in renin levels: during the intervention, the affected renal vein demonstrated significantly elevated renin levels compared to both the contralateral renal vein and inferior vena cava (p < 0.05), while post-intervention peripheral venous renin levels were significantly lower than pre-intervention values (p < 0.05).

Interventional therapy using thermosensitive embolic agents for pediatric renovascular hypertension caused by renal artery branch stenosis demonstrated significant clinical efficacy. It effectively improved the clinical symptoms, blood pressure control, target organ damage, and renin levels of the children, with no serious complications observed during follow-up. This provides a new option for clinical treatment.

Level of Evidence: Level 4, an uncontrolled clinical intervention study.

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** renal vascular hypertension (MESH:D006977), left ventricular hypertrophy (MESH:D017379), hypertension (MESH:D006973), renovascular hypertension (MESH:D006978), headache (MESH:D006261), renal artery branch stenosis (MESH:D012078), embolic (MESH:D004617)
- **Chemicals:** Scr (-), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12571592/full.md

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Source: https://tomesphere.com/paper/PMC12571592