12 results on '"de Bruijn, Clara M. A."'
Search Results
2. Teenagers’ and parental attitudes towards the use of placebo pills
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de Bruijn, Clara M. A., Benninga, Marc A., Vlieger, Arine M., Paediatric Gastroenterology, Amsterdam Gastroenterology Endocrinology Metabolism, and Amsterdam Reproduction & Development (AR&D)
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Pediatrics, Perinatology and Child Health ,Pediatric care ,Placebo - Abstract
The placebo response a significant therapeutic improvement after a placebo intervention — can be high in children. The question arises of how optimal advantages of placebo treatment in pediatric clinical care be achieved. In this era of shared-decision making, it is important to be aware of patients’ and parental attitudes. Therefore, the aim of the current study was to assess teenagers’ and parental views on the use of placebo pills in pediatric clinical care. All patients (aged 12–18 years) and parents of children (aged 0–18 years), visiting the pediatric outpatient clinic between March 2020 through December 2020, were invited to participate in this study multicenter survey study. Of 1644 distributed questionnaires: 200/478 (47%) teenagers and 456/1166 (45%) parents filled out the complete survey. More parents were positive towards prescribing placebo medication than teenagers (80% vs. 71%, p = .019), especially when the clinician disclosed the use of a placebo to parents and teenagers, respectively (76% vs. 55%, p = .019). Increasing age of teenagers was positively associated with the willingness for placebo interventions (OR 0.803, 95%CI 0.659–0.979), as was a higher level of parental education (OR 0.706, 95%CI 0.526–0.949). Conclusion: This study emphasizes the willingness of teenagers and parents to receive placebo medication. Placebo medication becoming more acceptable and integrated into daily care may contribute to a decrease in medication use. What is Known:• A placebo is a treatment without inherent power to produce any therapeutic effect, but can result in significant therapeutic improvement, the so-called placebo response.• Treatment response rates after placebo interventions in children can be high, ranging from 41 to 46% in pediatric trials. What is New:• Most teenagers (71%) and parents (80%) find it appropriate for healthcare professionals to prescribe placebo medication.• Compared to adult care, pediatrics has a unique feature to disclose placebo treatment to parents while concealing it for the young patient: the majority of teenagers (85%) and parents (91%) agree to disclose placebo treatment to parents exclusively.
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- 2023
3. Children with functional gastrointestinal disorders with and without co‐existing nausea: A comparison of clinical and psychological characteristics
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de Bruijn, Clara M. A., primary, Geijtenbeek, Anne, additional, Browne, Pamela D., additional, Benninga, Marc A., additional, and Vlieger, Arine M., additional
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- 2023
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4. Do Polymorphisms Predict Hypnotherapy Response in Children With Functional Abdominal Pain Disorders: An Explorative Study.
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de Bruijn, Clara M. A., Hovy, Stefan W., Tromp, Ellen, Benninga, Marc A., Hall, Kathryn T., and Vlieger, Arine M.
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- 2023
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5. Challenges and costs of donor screening for fecal microbiota transplantations
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Bénard, Mèlanie V., primary, de Bruijn, Clara M. A., additional, Fenneman, Aline C., additional, Wortelboer, Koen, additional, Zeevenhoven, Judith, additional, Rethans, Bente, additional, Herrema, Hilde J., additional, van Gool, Tom, additional, Nieuwdorp, Max, additional, Benninga, Marc A., additional, and Ponsioen, Cyriel Y., additional
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- 2022
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6. Pharmacologic Treatment in Functional Abdominal Pain Disorders in Children: A Systematic Review
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Rexwinkel, Robyn, primary, de Bruijn, Clara M. A., additional, Gordon, Morris, additional, Benninga, Marc A., additional, and Tabbers, Merit M., additional
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- 2021
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7. Pharmacologic Treatment in Functional Abdominal Pain Disorders in Children: A Systematic Review
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Rexwinkel, Robyn, de Bruijn, Clara M A, Gordon, Morris, Benninga, Marc A, Tabbers, Merit M, Rexwinkel, Robyn, de Bruijn, Clara M A, Gordon, Morris, Benninga, Marc A, and Tabbers, Merit M
- Abstract
Functional abdominal pain disorders (FAPDs) are common in childhood, impacting quality of life and school attendance. There are several compounds available for the treatment of pediatric FAPDs, but their efficacy and safety are unclear because of a lack of head-to-head randomized controlled trials (RCTs). To systematically review the efficacy and safety of the pharmacologic treatments available for pediatric FAPDs. Electronic databases were searched from inception to February 2021. RCTs or systematic reviews were included if the researchers investigated a study population of children (4-18 years) in whom FAPDs were treated with pharmacologic interventions and compared with placebo, no treatment, or any other agent. Two reviewers independently performed data extraction and assessed their quality. Any interresearcher disagreements in the assessments were resolved by a third investigator. Seventeen articles representing 1197 children with an FAPD were included. Trials investigating antispasmodics, antidepressants, antibiotics, antihistaminic, antiemetic, histamine-2-receptor antagonist, 5-HT4-receptor agonist, melatonin, and buspirone were included. No studies were found on treatment with laxatives, antidiarrheals, analgesics, antimigraines, and serotonergics. The overall quality of evidence on the basis of the Grading of Recommendations, Assessment, Development and Evaluations system was very low to low. On the basis of current evidence, it is not possible to recommend any specific pharmacologic agent for the treatment of pediatric FAPDs. However, agents such as antispasmodics or antidepressants can be discussed in daily practice because of their favorable treatment outcomes and the lack of important side effects. High-quality RCTs are necessary to provide adequate pharmacologic treatment. For future intervention trials, we recommend using homogenous outcome measures and instruments, a large sample size, and long-term follow-up. [Abstract copyright: Copyright © 2021 b
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- 2021
8. Development of a Bowel Management Scoring Tool in Pediatric Patients with Constipation
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de Bruijn, Clara M. A., Safder, Shaista, Rolle, Udo, Mosiello, Giovanni, Marshall, David, Christiansen, Albert B., Benninga, Marc A., Paediatric Gastroenterology, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, and ARD - Amsterdam Reproduction and Development
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bowel management ,children ,Surveys and Questionnaires ,Pediatrics, Perinatology and Child Health ,Quality of Life ,Humans ,Reproducibility of Results ,Child ,Constipation ,Fecal Incontinence - Abstract
Objective: To develop a reliable and valid scoring tool, the Pediatric Bowel Management Scoring Tool (PBMST), to better guide management of constipation in pediatric patients. Study design: The project comprised 2 stages, development of the questionnaire and construction of the bowel management score. Two questionnaires were created, one for children aged 8-18 years to self-report and one parent proxy-report for children aged 4-8 years. Questions regarding physical symptoms (n = 6), emotional aspects (n = 2), social activities/school (n = 1), and treatment (n = 1) were included. Patients (or parents of patients) with symptoms of constipation completed the questionnaire. The reproducibility of each question was computed using the Cohen weighted kappa coefficient (κ). A bowel management score was developed using logistic regression analysis, assessing the associations between the questions and impact on self-reported quality of life (QoL). Questions with adequate reproducibility and significantly associated with QoL were incorporated into the score. Results: The questionnaire was completed by 385 patients. Six questions met the inclusion criteria and were incorporated into the score: stool shape (range, 0-3 points), anorectal pain (0-4 points), abdominal pain (0-3 points), frequency of fecal incontinence (0-3 points), assistance of caregivers (0-3 points), and interference with social activities (0-6 points). Differences in bowel management scores among patients reporting no, little, some, or major impact on QoL were statistically significant (P
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- 2022
9. Discontinuation of imatinib in children with chronic myeloid leukaemia in sustained deep molecular remission: results of the STOP IMAPED study
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de Bruijn, Clara M. A., primary, Millot, Frédéric, additional, Suttorp, Meinolf, additional, Borisevich, Marina, additional, Brons, Paul, additional, Lausen, Birgitte, additional, and de Bont, Eveline S. J. M., additional
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- 2019
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10. The Use of Pictograms in the Evaluation of Functional Abdominal Pain Disorders in Children.
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de Bruijn CMA, Rexwinkel R, Vermeijden NK, Hoffman I, Tack J, and Benninga MA
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- Humans, Child, Nausea, Vomiting, Health Personnel, Abdominal Pain diagnosis, Abdominal Pain complications, Gastrointestinal Diseases complications
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Objective: To evaluate whether the use of pictograms improves symptom evaluation for children with functional abdominal pain disorders (FAPDs)., Study Design: This survey study was conducted in 2 academic centers and included patients aged 8-18 years visiting the outpatient clinic for FAPD symptom evaluation. Patients were randomized to fill out the questionnaire without or with accompanying pictograms to assess gastrointestinal symptoms. Afterwards, patients underwent clinical health assessment by the healthcare professional (HCP). Subsequently, the HCP filled out the same questionnaire without pictograms, while blinded to the questionnaire completed by the patient. Primary outcome was the level of agreement between identified symptoms as assessed by patients and HCP., Results: We included 144 children (questionnaire without accompanying pictograms [n = 82] and with accompanying pictograms [n = 62]). Overall agreements rates were not significantly different (without pictograms median, 70% vs with pictograms median, 70%). Accompanying pictograms did not significantly improve the assessment of abdominal pain symptoms. Accompanying pictograms were beneficial for concordance rates for nausea and vomiting symptoms (without pictograms median, 67% vs with pictograms median, 100%; P = .047). Subgroup analyses for children aged 8-12 years of age revealed similar results (concordance on the presence of nausea and vomiting without pictograms median, 67% vs with pictograms median, 100%; P = .015). Subgroup analyses for children ages 12-18 years showed no significant differences in concordance rates., Conclusions: Pictograms do not seem to improve the assessment of FAPDs. However, the use of pictograms improves the evaluation of nausea and vomiting, especially for children aged 8-12 years. Therefore, HCPs could consider using pictograms in that setting during consultations., Competing Interests: Declaration of Competing Interest M.B. is consultant for Shire, Norgine, Coloplast, Danone, Takeda, Allergan, Shire, FrieslandCampina, United Pharamceuticals, and HiPP. The other authors declare no conflicts of interest., (Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.)
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- 2023
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11. Teenagers' and parental individual needs for side effects information and the influence of nocebo effect education.
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de Bruijn CMA, Hamming GAC, Knibbe CAJ, Tromp E, Benninga MA, and Vlieger AM
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- Humans, Adolescent, Child, Parents, Attitude, Nocebo Effect, Drug-Related Side Effects and Adverse Reactions
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Objectives: When developing a policy on how information about medication and its side effects (SE) should be provided in pediatrics, it is crucial to know individual needs. This paper investigates teenagers' and parental attitudes on information on SE, before and after education on the nocebo effect (NE)., Methods: This multicenter survey study included 226 teenagers (12-18 years) and 525 parents of patients (0-18 years). Questions assessed demographics, clinical characteristics and attitudes towards the amount of SE information before and after the explanation of NE., Results: Before NE education, 679 (93 %) participants preferred to receive SE information: 337 (45 %) about all possible SE and 360 (48 %) desired specific information (i.e., severe, common, visible, or long-term SE). After NE explanation, significantly more participants (58 %) wished to receive information about all possible SE (p < .001). When explaining SE, teenagers preferred positive framing more than parents (64 % vs. 54 %, p = .043)., Conclusions: Most teenagers and parents wish to receive extensive SE information, even after explaining the NE, but variances in individual needs exist., Practice Implications: This study emphasizes the importance of tailor-made communication strategies for providing information on medications to parents and their children., Competing Interests: Declaration of interest No conflict of interests relevant to this article to disclose., (Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.)
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- 2023
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12. Skills or Pills: Randomized Trial Comparing Hypnotherapy to Medical Treatment in Children With Functional Nausea.
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Browne PD, de Bruijn CMA, Speksnijder EM, Hollander BD, van Wering HM, Wessels MMS, Groeneweg M, Goede J, Frankenhuis C, Tromp E, Benninga MA, and Vlieger AM
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- Adolescent, Child, Humans, Nausea therapy, Treatment Outcome, Dyspepsia therapy, Hypnosis
- Abstract
Background & Aims: The potential effectiveness of gut-directed hypnotherapy (HT) is unknown for pediatric chronic nausea. This randomized controlled trial compared HT with standard medical treatment (SMT)., Methods: One hundred children (ages, 8-18 y) with chronic nausea and fulfilling functional nausea (FN) or functional dyspepsia (FD) criteria were allocated randomly (1:1) to HT or SMT, with a 3-month intervention period. Outcomes were assessed at baseline, at the halfway point, after treatment, and at the 6- and 12-month follow-up evaluation. Children scored nausea symptoms in a 7-day diary. The primary outcome was treatment success, defined as a reduction in nausea of 50% or more, at the 12-month follow-up evaluation. Secondary outcomes included adequate relief of nausea., Results: After treatment and at the 6-month follow-up evaluation, there was a trend toward higher treatment success in the HT group compared with the SMT group (45% vs 26%, P = .052; and 57% vs 40%, P = .099, respectively). At 12 months, treatment success was similar in both groups (60% in the HT group and 55% in the SMT group; P = .667). In the FN group, significantly higher success rates were found for HT, but no differences were found in patients with FD. Adequate relief was significantly higher in the HT group than in the SMT group at the 6-month follow-up evaluation (children: 81% vs 55%, P = .014; parents: 79% vs 53%; P = .016), but not at the 12-month follow-up evaluation., Conclusions: HT and SMT were effective in reducing nausea symptoms in children with FN and FD. In children with FN, HT was more effective than SMT during and after the first 6 months of treatment. Therefore, HT and SMT, applied separately or in combination, should be offered to children with FN as a treatment option (Clinical trials registration number: NTR5814)., (Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.)
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- 2022
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