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René Wijnen

Biographic Data

ID7625555
NAMERené Wijnen
GIVEN NAMESRené
FAMILY NAMEWijnen
SIGNATUREWIJNEN R
AFFILIATIONSErasmus MC - Sophia Children’s Hospital
ORCID0000-0001-7266-9713
VERIFIEDYes
TOTAL WORKS5
TOTAL CITATIONS0
WORKS AS AUTHOR5
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2021
LATEST PUBLICATION YEAR2026
H-INDEX0
  • European Reference Networks as core health structures where referring genetic newborn screening positive infants

    Open Access•F Fortunato, Rita Selvatici et al.•ARTICLE•Frontiers in Public Health•2026

    Rare diseases (RDs), affecting fewer than 5 people per 10,000, present unique challenges to usual care pathways due to their unique characteristics: rarity and large number of disease entities, heterogeneous clinical manifestations and genetic causes, multisystemic involvement, and high complexity of diagnosis and treatment. This complexity often hampers the setting of appropriate pathways of care, which are not easily identifiable by patients an…

  • Psychometric Performance of the Stony Brook Scar Evaluation Scale and SCAR-Q Questionnaire in Dutch Children after Pediatric Surgery

    Open Access•Chantal A ten Kate, Hilde J H Koese et al.•ARTICLE•International Journal of…•2023

    Introduction: The growing population of survivors following pediatric surgery emphasizes the importance of long-term follow-up. The impact of surgical scars on daily life can be evaluated through patient-reported outcome measurements. The Stony Brook Scar Evaluation Scale (SBSES) and SCAR-Q questionnaire are two interesting instruments for this purpose. We evaluated their psychometric performance in Dutch children after pediatric surgery. Methods…

  • The Management of Asymptomatic Congenital Pulmonary Airway Malformation

    Open Access•Casper M Kersten, Sergei M Hermelijn et al.•ARTICLE•Children•2022

    Consensus on the optimal management of asymptomatic congenital pulmonary airway malformation (CPAM) is lacking, and comparison between studies remains difficult due to a large variety in outcome measures. We aimed to define a core outcome set (COS) for pediatric patients with an asymptomatic CPAM. An online, three-round Delphi survey was conducted in two stakeholder groups of specialized caregivers (surgeons and non-surgeons) in various European …

  • Psychometric Performance of a Condition-Specific Quality-of-Life Instrument for Dutch Children Born with Esophageal Atresia

    Open Access•Chantal A ten Kate, Hanneke IJsselstijn et al.•ARTICLE•Children•2022

    A condition-specific instrument (EA-QOL©) to assess quality of life of children born with esophageal atresia (EA) was developed in Sweden and Germany. Before implementing this in the Netherlands, we evaluated its psychometric performance in Dutch children. After Swedish−Dutch translation, cognitive debriefing was conducted with a subset of EA patients and their parents. Next, feasibility, reliability, and validity were evaluated in a nationwide f…

  • Patient-Reported Outcome Measures and Clinical Outcomes in Children with Foregut Anomalies

    Open Access•Isabel I Sreeram, Chantal A ten Kate et al.•ARTICLE•Children•2021

    Increasing numbers of children and adults with chronic disease status highlight the need for a value-based healthcare system. Patient-reported outcome measures (PROMs) are essential to value-based healthcare, yet it remains unclear how they relate to clinical outcomes such as health and daily functioning. We aimed to assess the added value of self-reported PROMs for health status (HS) and quality of life (QoL) in the long-term follow-up of childr…

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  • Patient-Reported Outcome Measures and Clinical Outcomes in Children with Foregut Anomalies

    Open Access•Isabel I Sreeram, Chantal A ten Kate et al.•ARTICLE•Children•2021

    Increasing numbers of children and adults with chronic disease status highlight the need for a value-based healthcare system. Patient-reported outcome measures (PROMs) are essential to value-based healthcare, yet it remains unclear how they relate to clinical outcomes such as health and daily functioning. We aimed to assess the added value of self-reported PROMs for health status (HS) and quality of life (QoL) in the long-term follow-up of childr…

  • The Management of Asymptomatic Congenital Pulmonary Airway Malformation

    Open Access•Casper M Kersten, Sergei M Hermelijn et al.•ARTICLE•Children•2022

    Consensus on the optimal management of asymptomatic congenital pulmonary airway malformation (CPAM) is lacking, and comparison between studies remains difficult due to a large variety in outcome measures. We aimed to define a core outcome set (COS) for pediatric patients with an asymptomatic CPAM. An online, three-round Delphi survey was conducted in two stakeholder groups of specialized caregivers (surgeons and non-surgeons) in various European …

  • Psychometric Performance of a Condition-Specific Quality-of-Life Instrument for Dutch Children Born with Esophageal Atresia

    Open Access•Chantal A ten Kate, Hanneke IJsselstijn et al.•ARTICLE•Children•2022

    A condition-specific instrument (EA-QOL©) to assess quality of life of children born with esophageal atresia (EA) was developed in Sweden and Germany. Before implementing this in the Netherlands, we evaluated its psychometric performance in Dutch children. After Swedish−Dutch translation, cognitive debriefing was conducted with a subset of EA patients and their parents. Next, feasibility, reliability, and validity were evaluated in a nationwide f…

  • Psychometric Performance of the Stony Brook Scar Evaluation Scale and SCAR-Q Questionnaire in Dutch Children after Pediatric Surgery

    Open Access•Chantal A ten Kate, Hilde J H Koese et al.•ARTICLE•International Journal of…•2023

    Introduction: The growing population of survivors following pediatric surgery emphasizes the importance of long-term follow-up. The impact of surgical scars on daily life can be evaluated through patient-reported outcome measurements. The Stony Brook Scar Evaluation Scale (SBSES) and SCAR-Q questionnaire are two interesting instruments for this purpose. We evaluated their psychometric performance in Dutch children after pediatric surgery. Methods…

  • European Reference Networks as core health structures where referring genetic newborn screening positive infants

    Open Access•F Fortunato, Rita Selvatici et al.•ARTICLE•Frontiers in Public Health•2026

    Rare diseases (RDs), affecting fewer than 5 people per 10,000, present unique challenges to usual care pathways due to their unique characteristics: rarity and large number of disease entities, heterogeneous clinical manifestations and genetic causes, multisystemic involvement, and high complexity of diagnosis and treatment. This complexity often hampers the setting of appropriate pathways of care, which are not easily identifiable by patients an…

Medicine (3 works) · Childhood Cancer Survivors' Quality of Life (2 works) · Clinical Psychology (2 works) · Clinical Psychology (2 works) · Congenital Diaphragmatic Hernia Studies (2 works) · Construct validity (2 works) · Esophageal and GI Pathology (2 works) · Pediatrics (2 works) · Physical therapy (2 works) · Psychometrics (2 works)

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