9 results on '"Claudia Elisabeth Kuehni"'
Search Results
2. Death certificate notifications in the Swiss Childhood Cancer Registry: assessing completeness and registration procedures
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Matthias Schindler, Vera Mitter, Eva Bergstraesser, Fabienne Gumy-Pause, Gisela Michel, Claudia Elisabeth Kuehni, and Swiss Paediatric Oncology Group (SPOG)
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paediatrics ,registry ,childhood cancer ,completeness ,Medicine - Abstract
QUESTIONS UNDER STUDY: Completeness is important in cancer registration. Identifying areas to improve registry procedures might help to maximise completeness. We examined characteristics of childhood cancer cases that were registered via death certificate notification (DCN) rather than during life, and estimated completeness of the Swiss Childhood Cancer Registry (SCCR). METHODS: We analysed data from all children who died from cancer in Switzerland between 1985–2009 at age
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- 2015
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3. Nuclear power plants and childhood leukaemia: lessons from the past and future directions
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Claudia Elisabeth Kuehni and Ben Daniel Spycher
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Cancer ,childhood ,leukaemia ,Ionising radiation ,nuclear power plants ,cancer registry ,Medicine - Abstract
In the 1980s, leukaemia clusters were discovered around nuclear fuel reprocessing plants in Sellafield and Dounreay in the United Kingdom. This raised public concern about the risk of childhood leukaemia near nuclear power plants (NPPs). Since then, the topic has been well-studied, but methodological limitations make results difficult to interpret. Our review aims to: (1.) summarise current evidence on the relationship between NPPs and risk of childhood leukaemia, with a focus on the Swiss CANUPIS (Childhood cancer and nuclear power plants in Switzerland) study; (2.) discuss the limitations of previous research; and (3.) suggest directions for future research. There are various reasons that previous studies produced inconclusive results. These include: inadequate study designs and limited statistical power due to the low prevalence of exposure (living near a NPP) and outcome (leukaemia); lack of accurate exposure estimates; limited knowledge of the aetiology of childhood leukaemia, particularly of vulnerable time windows and latent periods; use of residential location at time of diagnosis only and lack of data on address histories; and inability to adjust for potential confounders. We conclude that risk of childhood leukaemia around NPPs should continue to be monitored and that study designs should be improved and standardised. Data should be pooled internationally to increase the statistical power. More research needs to be done on other putative risk factors for childhood cancer such as low-dose ionizing radiation, exposure to certain chemicals and exposure to infections. Studies should be designed to allow examining multiple exposures.
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- 2014
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4. Predictors of asthma control differ from predictors of asthma attacks in children: the Swiss Paediatric Airway Cohort
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Cristina Ardura-Garcia, Maria Christina Mallet, Daria Olena Berger, Karin Hoyler, Anja Jochmann, Alena Kuhn, Alexander Moeller, Nicolas Regamey, Florian Singer, Eva Sophie Lunde Pedersen, Claudia Elisabeth Kuehni, and on behalf of SPAC Study Team
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immune system diseases ,respiratory tract diseases - Abstract
Background It is unclear if predictors of asthma attacks are the same as those of asthma symptom control in children. We evaluated predictors for these two outcomes in a clinical cohort study. Methods The Swiss Paediatric Airway Cohort (SPAC) is a multicentre prospective clinical cohort of children referred to paediatric pulmonologists. This analysis included 516 children diagnosed with asthma. At baseline, we collected sociodemographic information, symptoms, personal and family history and environmental exposures from a parental baseline questionnaire, and treatment and test results from hospital records. Outcomes were assessed 1 year later by parental questionnaire: asthma control in the last 4 weeks as defined by GINA guidelines, and asthma attacks defined as any unscheduled visit for asthma in the past year. We used logistic regression to identify and compare predictors for suboptimal asthma control and asthma attacks. Results At follow-up, 114/516 children (22%), reported suboptimal asthma control, and 114 (22%) an incident asthma attack. Only 37 (7%) reported both. Suboptimal asthma control was associated with poor symptom control at baseline, wheeze triggered by allergens, colds and exercise, a more intense treatment at baseline, history of preschool and persistent wheeze, and exposure to tobacco smoke. Incident asthma attacks were associated with previous episodes of severe wheeze and asthma attacks, younger age and non-Swiss origin. Lung function, exhaled nitric oxide (FeNO) and allergic sensitization at baseline were not associated with control or attacks. Conclusion Predictors of suboptimal control differ from those of attacks. Prediction tools and preventive efforts should differentiate these two asthma outcomes.
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- 2022
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5. Diagnosing Preclinical Cardiac Dysfunction in Swiss Childhood Cancer Survivors: Protocol for a Single-Center Cohort Study (Preprint)
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Christina Schindera, Claudia Elisabeth Kuehni, Mladen Pavlovic, Eva Simona Haegler-Laube, Daniel Rhyner, Nicolas Waespe, Jochen Roessler, Thomas Suter, and Nicolas Xavier von der Weid
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BACKGROUND Cardiovascular disease is the leading nonmalignant cause of late deaths in childhood cancer survivors. Cardiovascular disease and cardiac dysfunction can remain asymptomatic for many years, but eventually lead to progressive disease with high morbidity and mortality. Early detection and intervention are therefore crucial to improve outcomes. OBJECTIVE In our study, we aim to assess the prevalence of preclinical cardiac dysfunction in adult childhood cancer survivors using conventional and speckle tracking echocardiography; determine the association between cardiac dysfunction and treatment-related risk factors (anthracyclines, alkylating agents, steroids, cardiac radiation) and modifiable cardiovascular risk factors (abdominal obesity, hypertension); investigate the development of cardiac dysfunction longitudinally in a defined cohort; study the association between cardiac dysfunction and other health outcomes like pulmonary disease, endocrine disease, renal disease, quality of life, fatigue, strength and endurance, and physical activity; and gain experience conducting a clinical study of childhood cancer survivors that will be extended to a national, multicenter study of cardiac complications. METHODS For this retrospective cohort study, we will invite ≥5-year childhood cancer survivors who were treated at the University Children's Hospital Bern, Switzerland with any chemotherapy or cardiac radiation since 1976 and who are ≥18 years of age at the time of the study for a cardiac assessment at the University Hospital Bern. This includes 544 childhood cancer survivors, of whom about half were treated with anthracyclines and/or cardiac radiation and half with any other chemotherapy. The standardized cardiac assessment includes a medical history focusing on signs of cardiovascular disease and its risk factors, a physical examination, anthropometry, vital parameters, the 1-minute sit-to-stand test, and echocardiography including 2-dimensional speckle tracking. RESULTS We will invite 544 eligible childhood cancer survivors (median age at the time of the study, 32.5 years; median length of time since diagnosis, 25.0 years) for a cardiac assessment. Of these survivors, 300 (55%) are at high risk, and 244 (45%) are at standard risk of cardiac dysfunction. CONCLUSIONS This study will determine the prevalence of preclinical cardiac dysfunction in Swiss childhood cancer survivors, inform whether speckle tracking echocardiography is more sensitive to cardiac dysfunction than conventional echocardiography, and give a detailed picture of risk factors for cardiac dysfunction. The results will help improve primary treatment and follow-up care of children with cancer. CLINICALTRIAL ClinicalTrials.gov NCT03790943; https://clinicaltrials.gov/ct2/show/NCT03790943 INTERNATIONAL REGISTERED REPORT DERR1-10.2196/17724
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- 2020
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6. Nutritional assessment in childhood cancer survivors: SCCSS-Nutrition study protocol (Preprint)
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Fabiën Naomi Belle, Maja Beck Popovic, Marc Ansari, Maria Otth, Claudia Elisabeth Kuehni, and Murielle Bochud
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BACKGROUND Childhood cancer survivors (CCSs) are at high risk of developing adverse late health effects. Poor nutritional intake may contribute to this risk, but information about dietary intake is limited. OBJECTIVE This study will assess dietary intake of CCSs and compare two dietary assessment tools: a self-reported food frequency questionnaire (FFQ), and dietary measurements from urine spot samples. METHODS In the Swiss Childhood Cancer Survivor Study, we assessed dietary intake of CCSs via a validated FFQ. To a subset of CCSs from the French-speaking region of Switzerland, we sent a urine spot collection kit to analyse urinary sodium, potassium, urea, urate, creatinine, and phosphate content. We will compare the FFQ with the urine spot analyses to quantify the intake of different nutrients in CCSs. Data collection took place between March 2016 and March 2018. RESULTS We contacted 1599 CCSs of whom 919 (57%) returned an FFQ. We excluded 11 CCSs who were pregnant or were breastfeeding, 35 CCSs with missing dietary data, and 71 CCSs who had unreliable FFQ data, resulting in 802 CCSs available for FFQ analyses. To a subset of 197 CCSs in French-speaking Switzerland we sent a urine spot collection kit, and 111 (56%) returned a urine sample. We expect to have the results from analyses of these samples in mid-2019. CONCLUSIONS The SCCSS-Nutrition study has collected in-depth dietary data that will allow us to assess dietary intake and quality and compare two dietary assessment tools. This study will contribute to the current knowledge of nutrition among CCSs and is a step towards surveillance guidelines and targeted nutritional recommendations for CCSs in Switzerland. CLINICALTRIAL ClinicalTrials.gov identifier SCCSS: NCT03297034
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- 2019
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7. Pregnancy and Birth Cohort Resources in Europe: a Large Opportunity for Aetiological Child Health Research
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Pernille Stemann, Larsen, Mads, Kamper-Jørgensen, Ashley, Adamson, Henrique, Barros, Jens Peter, Bonde, Sonia, Brescianini, Sinead, Brophy, Maribel, Casas, Marie-Aline, Charles, Graham, Devereux, Merete, Eggesbø, Maria Pia, Fantini, Urs, Frey, Ulrike, Gehring, Regina, Grazuleviciene, Tine Brink, Henriksen, Irva, Hertz-Picciotto, Barbara, Heude, Daniel O, Hryhorczuk, Hazel, Inskip, Vincent W V, Jaddoe, Debbie A, Lawlor, Johnny, Ludvigsson, Cecily, Kelleher, Wieland, Kiess, Berthold, Koletzko, Claudia Elisabeth, Kuehni, Inger, Kull, Henriette Boye, Kyhl, Per, Magnus, Isabelle, Momas, Dierdre, Murray, Juha, Pekkanen, Kinga, Polanska, Daniela, Porta, Gry, Poulsen, Lorenzo, Richiardi, Nel, Roeleveld, Anne Mette, Skovgaard, Radim J, Sram, Katrine, Strandberg-Larsen, Carel, Thijs, Manon, Van Eijsden, John, Wright, Martine, Vrijheid, Anne-Marie Nybo, Andersen, Pernille Stemann Larsen, Mads Kamper-Jørgensen, Ashley Adamson, Henrique Barro, Jens Peter Bonde, Sonia Brescianini, Sinead Brophy, Maribel Casa, Graham Devereux, Merete Eggesbø, Maria Pia Fantini, Urs Frey, Ulrike Gehring, Regina Grazuleviciene, Tine Brink Henriksen, Irva Hertz-Picciotto, Barbara Heude, Daniel O. Hryhorczuk, Hazel Inskip, Vincent W.V. Jaddoe, Debbie A Lawlor, Johnny Ludvigsson, Cecily Kelleher, Wieland Kie, Berthold Koletzko, Claudia Elisabeth Kuehni, Inger Kull, Henriette Boye Kyhl, Per Magnu, Isabelle Moma, Dierdre Murray, Juha Pekkanen, Kinga Polanska, Daniela Porta, Gry Poulsen, Lorenzo Richiardi, Nel Roeleveld, Anne Mette Skovgaard, Radim J. Sram, Katrine Strandberg-Larsen, Carel Thij, Manon Van Eijsden, John Wright, Martine Vrijheid, Anne-Marie Nybo Andersen, Erasmus MC other, Dermatology, Epidemiologie, and RS: CAPHRI School for Public Health and Primary Care
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Biomedical Research ,Databases, Factual ,Infant Welfare ,Infant, Newborn ,Infant ,Human Reproducion Genomic disorders and inherited multi-system disorders [NCEBP 12] ,BIRTH COHORTS ,Cohort Studies ,Europe ,cohort characteristics ,European pregnancy birth cohort ,PREGNANCY ,Pregnancy ,Child, Preschool ,Health Resources ,Humans ,Female ,cross-cohort collaboration ,Child ,AETIOLOGY - Abstract
Item does not contain fulltext BACKGROUND: During the past 25 years, many pregnancy and birth cohorts have been established. Each cohort provides unique opportunities for examining associations of early-life exposures with child development and health. However, to fully exploit the large amount of available resources and to facilitate cross-cohort collaboration, it is necessary to have accessible information on each cohort and its individual characteristics. The aim of this work was to provide an overview of European pregnancy and birth cohorts registered in a freely accessible database located at http://www.birthcohorts.net. METHODS: European pregnancy and birth cohorts initiated in 1980 or later with at least 300 mother-child pairs enrolled during pregnancy or at birth, and with postnatal data, were eligible for inclusion. Eligible cohorts were invited to provide information on the data and biological samples collected, as well as the timing of data collection. RESULTS: In total, 70 cohorts were identified. Of these, 56 fulfilled the inclusion criteria encompassing a total of more than 500,000 live-born European children. The cohorts represented 19 countries with the majority of cohorts located in Northern and Western Europe. Some cohorts were general with multiple aims, whilst others focused on specific health or exposure-related research questions. CONCLUSION: This work demonstrates a great potential for cross-cohort collaboration addressing important aspects of child health. The web site, http://www.birthcohorts.net, proved to be a useful tool for accessing information on European pregnancy and birth cohorts and their characteristics.
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- 2013
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8. Household income and risk-of-poverty of parents of long-term childhood cancer survivors
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Luzius, Mader, Katharina, Roser, Julia, Baenziger, Eva Maria, Tinner, Katrin, Scheinemann, Claudia Elisabeth, Kuehni, and Gisela, Michel
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Male ,Parents ,Adolescent ,Infant ,Cost of Illness ,Socioeconomic Factors ,Child, Preschool ,Neoplasms ,Surveys and Questionnaires ,Humans ,Female ,Survivors ,Child ,Poverty ,Switzerland - Abstract
Taking care of children diagnosed with cancer affects parents' professional life and may place the family at risk of poverty. We aimed to (i) compare the household income and risk of poverty of parents of childhood cancer survivors (CCS) to parents of the general population and (ii) identify sociodemographic and cancer related factors associated with risk of poverty. As part of the Swiss Childhood Cancer Survivor Study we sent a questionnaire to parents of CCS aged 5 15 years who survived =5 years after diagnosis. Information on parents of the general population came from the Swiss Household Panel (parents with =1 child aged 5 15 years). Risk of poverty was defined as having a monthly household income of
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- 2017
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9. Properdin in childhood and its association with wheezing and atopy
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Kathryn Grace, Staley, Claudia Elisabeth, Kuehni, Marie-Pierre Françoise, Strippoli, Teresa, McNally, Michael, Silverman, and Cordula, Stover
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Male ,Properdin ,Complement Pathway, Alternative ,White People ,Sex Factors ,Asian People ,Genes, X-Linked ,Case-Control Studies ,Hypersensitivity ,Humans ,Female ,Child ,Genetic Association Studies ,Respiratory Sounds ,Skin Tests - Abstract
Properdin, a serum glycoprotein, is an important component of innate immunity, the only known positive regulator of complement, acting as an initiation point for alternative pathway activation. As an X-linked protein, we hypothesized that properdin may play a modulatory role in the pathogenesis of viral wheeze in children, which tends to be more common and more severe in boys. We aimed to determine properdin levels in a community-based paediatric sample, and to assess whether levels of properdin were associated with childhood wheeze phenotypes and atopy. We studied 137 school-children aged 8-12 yrs, a nested sample from a cohort study. Properdin was measured by a commercial enzyme-linked immunoabsorbant assay. We assessed wheeze by questionnaire, validated it by a nurse-led interview and performed skin prick tests and a methacholine challenge in all children. Forty children (29%) reported current wheeze. Serum properdin levels ranged between 18 and 40 microg/ml. Properdin was not associated with age, gender, atopy, bronchial responsiveness, current wheeze (neither the viral wheeze nor multiple-trigger wheeze phenotype) or severity of wheeze, but was slightly lower in south Asian (median 21.8 microg/ml) compared with white children (23.3 microg/ml; p = 0.006). Our data make it unlikely that properdin deficiency is common in healthy children or that levels of properdin are a major risk factor for wheeze or atopy.
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- 2010
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