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Dive into the research topics where Corine Penning is active.

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Featured researches published by Corine Penning.


Journal of The American Dietetic Association | 2010

Enteral Nutrition in Children with Short-Bowel Syndrome: Current Evidence and Recommendations for the Clinician

Joanne Olieman; Corine Penning; Hanneke IJsselstijn; Johanna C. Escher; Koen Joosten; Jessie M. Hulst; Dick Tibboel

The optimal enteral feeding regimen in children with short-bowel syndrome (SBS) is debated by clinicians. The purpose of this article is to present an overview of published data on feeding strategies in children with SBS. A structured literature search (years 1966 through 2007) was done to identify human studies in children directly addressing nutrition (or specified nutrients) in relation to SBS. Eight relevant studies retrieved were graded by seven experts according to the Scottish Intercollegiate Guidelines Network criteria. This grading system is based on the study design and methodological quality of individual studies. Recommendations were made based on the outcome according to the Scottish Intercollegiate Guidelines Network if appropriate and on expert opinion otherwise. The most important recommendations are: Enteral nutrition should be initiated as soon as possible after bowel resection to promote intestinal adaptation. Enteral nutrition should be administered in a continuous fashion. Breast milk or standard polymeric formula (depending on the childs age) is recommended as preferred type of nutrition. Bottle-feeding (small volumes) should be started as soon as possible in neonates to stimulate the suck and swallow reflexes. Solid food can be introduced at the age of 4 to 6 months (corrected for gestational age if necessary) to stimulate oral motor activity and to avoid feeding aversion behavior. The team of experts concluded that high-quality research on the preferred types of enteral and oral nutrition in children with SBS is scarce. Multicenter prospective studies on the effects of feeding strategies on bowel adaptation, fecal production, linear growth, and clinical outcome are required to find the optimal feeding regimen in children with SBS.


Developmental Medicine & Child Neurology | 2010

Prevalence and clinical presentation of constipation in children with severe generalized cerebral palsy.

Rebekka Veugelers; Marc A. Benninga; Elsbeth A. C. Calis; Sten P. Willemsen; Heleen M. Evenhuis; Dick Tibboel; Corine Penning

Aimu2002 Our aim was to study the prevalence and characteristics of constipation in children with profound multiple disabilities, as data in this area are scarce.


The American Journal of Clinical Nutrition | 2011

Measuring body composition and energy expenditure in children with severe neurologic impairment and intellectual disability

Rob Rieken; Johannes B. van Goudoever; Henk Schierbeek; Sten P. Willemsen; Elsbeth A. C. Calis; Dick Tibboel; Heleen M. Evenhuis; Corine Penning

BACKGROUNDnAccurate prediction equations for estimating body composition and total energy expenditure (TEE) in children with severe neurologic impairment and intellectual disability are currently lacking.nnnOBJECTIVEnThe objective was to develop group-specific equations to predict body composition by using skinfold-thickness measurements and bioelectrical impedance analysis (BIA) and to predict TEE by using data on mobility, epilepsy, and muscle tone.nnnDESIGNnMeasures of body composition with the use of skinfold-thickness measurements (percentage of body fat) and BIA (total body water) were compared with those from isotope dilution (reference method) by using intraclass correlation coefficients (ICCs) and Bland and Altman limits of agreement analyses. With the use of the same methods, the outcomes of cerebral palsy-specific TEE equations were compared with those of the doubly labeled water method (reference method). Group-specific regression equations were developed by using forward-stepwise-multiple-correlation-regression analyses.nnnRESULTSnSixty-one children with a mean (±SD) age of 10.1 ± 4.3 y (32 boys) were studied. A new equation based on the sum of 4 skinfold-thickness measurements did not improve agreement (n = 49; ICC = 0.61), whereas the newly developed BIA equation-which includes tibia length as an alternative for standing height-did improve agreement (n = 61; ICC = 0.96, SEE = 1.7 kg, R(2) = 0.92). The newly developed TEE equation, which uses body composition, performed better (n = 52; ICC = 0.87, SEE = 180 kcal, R(2) = 0.77) than did the equation of Schofield (n = 52; ICC = 0.82, SEE = 207 kcal, R(2) = 0.69).nnnCONCLUSIONSnCurrent cerebral palsy-specific equations for measuring body composition and energy expenditure are inaccurate. BIA is more accurate at assessing nutritional status in this population than is the measurement of skinfold thickness. The newly developed TEE equation, which uses body composition, provides a reasonable estimate of energy expenditure in these children despite its variability.


Ajidd-american Journal on Intellectual and Developmental Disabilities | 2009

Prevalence of cardiovascular risk factors in older people with intellectual disability.

Channa F. de Winter; Karla W. Magilsen; J. Claudia van Alfen; Corine Penning; Heleen M. Evenhuis

The prevalence and correlates of cardiovascular risk factors in older adults with intellectual disability was examined. We conducted a cross-sectional study with 50- to 90-year-old clients (N = 470) of three Dutch intellectual disability care providing organizations and found that healthy behavior was low, with 98.9% of the participants having an unhealthy diet and 68.3%, a lack of exercise. Smoking (13.6%) and alcohol abuse (0.3%) were relatively minor problems. Abdominal overweight (70.4%), diabetes (8.7%), hypertension (36.8%), and hypercholesterolemia (31.8%) were highly prevalent. These profiles have important implications in determining the risk of cardiovascular disease in people with intellectual disability. Campaigns to promote health should be focused on education and the introduction of preventive screening programs.


Journal of Pediatric Surgery | 2010

Interdisciplinary management of infantile short bowel syndrome: resource consumption, growth, and nutrition

Joanne Olieman; Marten J. Poley; Saskia J. Gischler; Corine Penning; Johanna C. Escher; Thelma L. van den Hoonaard; Johannes B. van Goudoever; N. M. A. Bax; Dick Tibboel; Hanneke IJsselstijn

BACKGROUND/PURPOSEnTo date, there are hardly any data on the treatment costs of infantile short bowel syndrome (SBS), despite growing interest in evidence-based and cost-effective medicine. Therefore, the aim of the study was to evaluate resource consumption and costs, next to studying nutritional and growth outcomes, in children with SBS who were treated by an interdisciplinary short bowel team.nnnMETHODSnData were collected for 10 children with infantile SBS (<or=1 year of age) born between 2002 and 2007. Data included demographic and medical data of the first admission and data on resource consumption, growth, and type of nutrition for the total follow-up period. Real economic costs were calculated in Euro (euro) and US dollar (


BMC Pediatrics | 2005

A population-based nested case control study on recurrent pneumonias in children with severe generalized cerebral palsy: ethical considerations of the design and representativeness of the study sample

Rebekka Veugelers; Elsbeth A. C. Calis; Corine Penning; Arianne P. Verhagen; Roos Bernsen; Jan Bouquet; Marc A. Benninga; Peter Merkus; H.G.M. Arets; Dick Tibboel; Heleen M. Evenhuis

).nnnRESULTSnSeven of the 10 patients were discharged with home parenteral nutrition. Total follow-up varied between 9 months and 5.5 years (median, 1.5 years). Six patients could be weaned off parenteral nutrition and 5 patients off enteral tube feeding, resulting in full oral intake. Seven patients had normal growth. Median duration of initial hospital admission was 174 days, and average costs of initial admission amounted to euro166,045 (


Journal of Pediatric Surgery | 2008

Growth and nutritional aspects of infantile short bowel syndrome for the past 2 decades

Joanne Olieman; Dick Tibboel; Corine Penning

218,681). Average total costs were euro269,700 (


Journal of Clinical Nursing | 2011

Is the temporal artery thermometer a reliable instrument for detecting fever in children

Corine Penning; Jan H van der Linden; Dick Tibboel; Heleen M. Evenhuis

355,195), reaching to a maximum of euro455,400 (


Journal of Pediatric Surgery | 2012

Impact of infantile short bowel syndrome on long-term health-related quality of life: A cross-sectional study

Joanne Olieman; Corine Penning; Marten J. Poley; Elisabeth M. W. J. Utens; Wim C. J. Hop; Dick Tibboel

599,762). These costs mainly comprised hospital admissions (82%), followed by nutrition (12%), surgical interventions (5%), and outpatient visits (1%).nnnCONCLUSIONSnThis study is among the first to describe resource consumption and costs in infants with SBS, examining real economic costs and extending beyond the initial hospitalization. Treatment of SBS requires considerable resource consumption, especially when patients depend on parenteral nutrition. Because the costs mainly comprise those of hospital admissions, early home parenteral nutrition could contribute to costs reduction. Interdisciplinary teams have the potential to facilitate early home parenteral nutrition and thus may reduce health care costs.


Pediatric Pulmonology | 2006

Should we use criteria or eyeballing to reject post-interruption tracings?

Rebekka Veugelers; Corine Penning; Stefan P.J. Grootscholten; Peter Merkus; H.G.M. Arets; Rob Rieken; J. E. Brussee; Mayke Jilderda-Janssen; Dick Tibboel; Heleen M. Evenhuis

BackgroundIn children with severe generalized cerebral palsy, pneumonias are a major health issue. Malnutrition, dysphagia, gastro-oesophageal reflux, impaired respiratory function and constipation are hypothesized risk factors. Still, no data are available on the relative contribution of these possible risk factors in the described population. This paper describes the initiation of a study in 194 children with severe generalized cerebral palsy, on the prevalence and on the impact of these hypothesized risk factors of recurrent pneumonias.Methods/DesignA nested case-control design with 18 months follow-up was chosen. Dysphagia, respiratory function and constipation will be assessed at baseline, malnutrition and gastro-oesophageal reflux at the end of the follow-up. The study population consists of a representative population sample of children with severe generalized cerebral palsy. Inclusion was done through care-centres in a predefined geographical area and not through hospitals. All measurements will be done on-site which sets high demands on all measurements. If these demands were not met in gold standard methods, other methods were chosen. Although the inclusion period was prolonged, the desired sample size of 300 children was not met. With a consent rate of 33%, nearly 10% of all eligible children in the Netherlands are included (n = 194). The study population is subtly different from the non-participants with regard to severity of dysphagia and prevalence rates of pneumonias and gastro-oesophageal reflux.DiscussionEthical issues complicated the study design. Assessment of malnutrition and gastro-oesophageal reflux at baseline was considered unethical, since these conditions can be easily treated. Therefore, we postponed these diagnostics until the end of the follow-up. In order to include a representative sample, all eligible children in a predefined geographical area had to be contacted. To increase the consent rate, on-site measurements are of first choice, but timely inclusion is jeopardised. The initiation of this first study among children with severe neurological impairment led to specific, unexpected problems. Despite small differences between participants and non-participating children, our sample is as representative as can be expected from any population-based study and will provide important, new information to bring us further towards effective interventions to prevent pneumonias in this population.

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Dick Tibboel

Erasmus University Rotterdam

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Heleen M. Evenhuis

Erasmus University Rotterdam

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Joanne Olieman

Boston Children's Hospital

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Elsbeth A. C. Calis

Erasmus University Rotterdam

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Marc A. Benninga

Boston Children's Hospital

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Rebekka Veugelers

Erasmus University Rotterdam

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Sten P. Willemsen

Erasmus University Rotterdam

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Johanna C. Escher

Boston Children's Hospital

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