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Published on: November 11, 2022
Intravenous Hydralazine in Hospitalized Children and Adolescents with Hypertension
Joseph T Flynn1, Miranda C Bradford2, Eric M Harvey3
1Division of Nephrology, Seattle Children's Hospital, Seattle, WA.
Insights
Intravenous hydralazine effectively lowered blood pressure in most hospitalized children. However, a significant number experienced excessive blood pressure reduction, indicating a need for careful dosing and monitoring.
Area of Science:
- Pediatric Nephrology
- Pediatric Cardiology
- Clinical Pharmacology
Background:
- Hypertension in hospitalized children is a significant clinical concern.
- Intravenous (IV) hydralazine is a commonly used agent for managing acute hypertension in pediatric populations.
- Understanding the efficacy and safety profile of IV hydralazine in children is crucial for optimizing treatment strategies.
Purpose of the Study:
- To evaluate the effectiveness of IV hydralazine in reducing blood pressure (BP) in hospitalized children.
- To assess the safety of IV hydralazine, including the incidence of adverse events.
- To identify factors associated with ideal BP response and excessive BP reduction.
Main Methods:
- Retrospective data collection from hospitalized children treated with IV hydralazine.
- Calculation of percent changes in blood pressure (BP) and mean arterial pressure (MAP).
- Use of linear and bivariate logistic regression to analyze associations between BP changes, clinical variables, and response outcomes (ideal clinical response and excess response).
Main Results:
- A total of 141 IV hydralazine doses were analyzed in children (median age 8 years), many with underlying renal disease, malignancy, or post-transplant status.
- The mean reduction in MAP was 19% ± 12%, with an ideal clinical response (10%-25% MAP reduction) in 47% of patients.
- Excessive response (>25% MAP reduction) occurred in 31% of children; higher initial MAP and hydralazine dose were associated with both ideal and excessive responses.
Conclusions:
- IV hydralazine demonstrates efficacy in reducing BP in the majority of hospitalized pediatric patients.
- A notable proportion of children experienced excessive BP reduction, highlighting the need for cautious administration and monitoring.
- Further research may be warranted to refine dosing guidelines and identify predictors of response in diverse pediatric populations.
Objectives:
To explore the efficacy and safety of intravenous (IV) hydralazine in hospitalized children with hypertension.
Study Design:
Data were retrospectively collected on hospitalized children treated with IV hydralazine. Percent changes in blood pressure (BP) were calculated, and linear regression was used to investigate associations between BP change and pertinent clinical and demographic variables. Bivariate logistic regression was used to investigate associations between the same covariates and the outcomes of ideal clinical response (ICR), a 10%-25% reduction in mean arterial pressure (MAP), and excess response (ER), a 25% reduction in MAP.
Results:
A total of 141 initial doses of IV hydralazine (median dose, 0.10 mg/kg [IQR, 0.09-0.11; range, 0.02-0.37]) were analyzed. Median age was 8 years (IQR, 2-15; range, 0-24); most patients had renal disease, malignancy, or were organ transplant recipients. The mean MAP reduction was 19% ± 12%. An ICR occurred in 66 patients (47%). Higher initial MAP and increased hydralazine dose were associated with greater percentage decrease in MAP. No association was found between ICR and the covariates of interest; higher initial MAP was associated with greater odds of ICR. ER occurred in 44 children (31%). Among this group, higher initial MAP and higher hydralazine dose were associated with increased odds of ER, and administration of other antihypertensive drugs was associated with decreased odds of ER. Four adverse effects possibly related to IV hydralazine, including 2 episodes of hypotension, were recorded.
Conclusions:
IV hydralazine reduced BP in the majority of children. However, a substantial proportion of children experienced potentially excessive BP reduction.
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