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Twenty-Four-Hour Urinary Sodium Excretion Predicts Therapeutic Effectiveness of Oral Rehydration Saline in Pediatric
Xiaojuan Du1, Chunyan Tao1, Yaru Wang1
1Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
Insights
Lower 24-hour urinary sodium excretion predicts successful oral rehydration saline treatment in children with vasovagal syncope. This finding offers a useful biomarker for predicting treatment response in pediatric patients.
Area of Science:
- Pediatrics
- Cardiology
- Nephrology
Background:
- Vasovagal syncope is common in children.
- Oral rehydration saline is a treatment option, but predicting effectiveness is challenging.
Purpose of the Study:
- To investigate if 24-hour urinary sodium excretion can predict the therapeutic effectiveness of oral rehydration saline in pediatric vasovagal syncope.
- To identify a potential biomarker for treatment response.
Main Methods:
- Eighty children with vasovagal syncope receiving oral rehydration saline were studied.
- Pre-treatment variables, including 24-hour urinary sodium excretion, were compared between responders and non-responders.
- Binary logistic regression and ROC curve analysis were used to assess predictive value.
Main Results:
- Responders (33) had lower pre-treatment 24-hour urinary sodium excretion (74 ± 29 mmol/24 h) compared to non-responders (47) (109 (93, 141) mmol/24 h).
- Baseline 24-hour urinary sodium excretion showed a positive correlation with head-up tilt test response time.
- A cut-off value of 83 mmol/24 h predicted therapeutic effectiveness with 87% sensitivity and 73% specificity (AUC=0.842).
Conclusions:
- 24-hour urinary sodium excretion is a valuable biomarker for predicting oral rehydration saline effectiveness in pediatric vasovagal syncope.
- This biomarker can aid in tailoring treatment strategies for affected children.
Abstract:
The study was designed to explore whether 24-hour urinary sodium excretion could predict the therapeutic effectiveness of oral rehydration saline in pediatric cases of vasovagal syncope. Eighty children suffering from vasovagal syncope with oral rehydration saline treatment in Department of Pediatrics, Peking University First Hospital, China, were recruited into the study. They were followed up for 3 (2, 3) months after treatment. Pre-treatment demographic, clinical, head-up tilt test-based hemodynamic and laboratory variables were compared between responders and non-responders. After univariate analysis, variables with p value < 0.05 in the comparison between responders and non-responders were further analyzed by binary logistic regression analysis. Receiver operating characteristic (ROC) curve was conducted to assess the value in predicting effectiveness of oral rehydration saline treatment. The results showed that 33 cases were responders, and 47 were non-responders. Blood sodium (138 ± 2 mmol/L vs. 139 ± 2 mmol/L, p < 0.05) and pre-treatment 24-hour urinary sodium excretion (74 ± 29 mmol/24 h vs. 109 (93, 141) mmol/24 h, p < 0.001) were lower in responders than in non-responders. The baseline 24-hour urinary sodium excretion was positively correlated to the duration from tilting to the positive response appearance in head-up tilt test (r = 0.289, p < 0.01). The cut-off value of baseline 24-hour urinary sodium excretion of the therapeutic effectiveness of oral rehydration saline on vasovagal syncope cases was 83 mmol/24 h, yielding a sensitivity of 87% and a specificity of 73% with AUC of 0.842 (p < 0.001). In conclusion, 24-hour urinary sodium excretion could be a useful biomarker to predict the therapeutic response to oral rehydration saline in pediatric cases of vasovagal syncope.
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