Saskia N. De Wildt (Netherlands)

Radboudumc Pharmacology - Toxicology
Dr de Wildt is full professor of Clinical Pharmacology and pediatric intensivist at Radboud University Medical Center. After a Medicine degree from University of Maastricht, and a PhD at Erasmus University Rotterdam, ‘Developmental aspects of midazolam metabolism’, she obtained board-certification in Pediatrics, Pediatric Intensive Care and Clinical Pharmacology (ErasmusMC Rotterdam, SickKids Toronto). Her research aims to better understand the impact of age, disease and genetics on drug disposition and to individualize drug dosing in children with a focus on pain&sedation and acute kidney injury. Her leadership roles in EU funded pediatric research infrastructure projects further contribute to the availability of medicines for children. She has >180 peer-reviewed publications and received >8 million euros (co) PI research funding from national funders, EU and Bill & Melinda Gates foundation. Dr. de Wildt is director of the Dutch Knowledge Center for Pharmacotherapy in Children (‘kinderformularium.nl’) and its international affiliates.

Author Of 4 Presentations

07:37 PM - 07:47 PM

DIAGNOSIS OF AKI USING IOHEXOL IN CRITICALLY ILL CHILDREN AND NEONATES: PRELIMINARY RESULTS OF THE HERO STUDY.

Lecture Time
07:37 PM - 07:47 PM

Abstract

Background and Aims

Up to 35% of all PICU and NICU patients will develop acute kidney injury (AKI), which is associated with a poor outcome and thus emphasizes the importance of an early diagnosis. However, this prevalence is based on estimation of GFR (eGFR) using serum creatinine, which is known to be inaccurate and may reflect an overestimation of GFR in this population. We aimed to test our hypothesis that AKI prevalence will be higher in critically ill children when using measured GFR (mGFR) based on iohexol clearance, than using eGFR and to investigate agreement between methods.

Methods

Term-born neonates and children admitted to the ICU with at least one failing organ were included. mGFR was calculated using a plasma disappearance curve after injection of iohexol. In parallel, eGFR was estimated using the bedside Schwartz equation (40*height(cm)/serum creatinine(µmol/L). Patients were diagnosed with AKI when serum creatinine, eGFR or mGFR values exceeded mean age specific reference values +1SD or were below 150% of the median, respectively. Agreement between methods was determined using Bland-Altman-Plots.

Results

Nineteen neonates (median age 2(range 1-21)days) and 21 children (8(0-17)years) were included. mGFR based diagnosis did not lead to a higher prevalence of AKI. Yet, prevalences varied greatly among PICU and NICU patients and between used methods (range 5.3-47.7%). Bland-Altman plots show moderate agreement between mGFr and eGFR(figure1).

combined figure espnic hero.jpg

Conclusions

When using iohexol based mGFR, the prevalence of AKI was not higher compared to eGFR based prevalence in our population. However, AKI appears very prevalent in PICU but less in term NICU patients.

Hide
10:12 AM - 10:32 AM

EXTREMELY LOW BIRTHWEIGHT INFANT: IS DRUG DOSING REALLY DIFFERENT?

Lecture Time
10:12 AM - 10:32 AM
01:07 PM - 01:31 PM

DO WE NEED TO TAKE THE DEGREE OF ILLNESS INTO ACCOUNT FOR DRUG DOSING?

Lecture Time
01:07 PM - 01:31 PM
02:20 PM - 02:40 PM

CLINICAL TRIALS IN THE NICU AND PICU: THE IDEAL WORLD IS REALLY FEASIBLE

Lecture Time
02:20 PM - 02:40 PM

Presenter of 3 Presentations

10:12 AM - 10:32 AM

EXTREMELY LOW BIRTHWEIGHT INFANT: IS DRUG DOSING REALLY DIFFERENT?

Lecture Time
10:12 AM - 10:32 AM
01:07 PM - 01:31 PM

DO WE NEED TO TAKE THE DEGREE OF ILLNESS INTO ACCOUNT FOR DRUG DOSING?

Lecture Time
01:07 PM - 01:31 PM
02:20 PM - 02:40 PM

CLINICAL TRIALS IN THE NICU AND PICU: THE IDEAL WORLD IS REALLY FEASIBLE

Lecture Time
02:20 PM - 02:40 PM