962 research outputs found
Commentary: Numerous, heterogeneous, and often poor—the studies on childhood leukaemia and socioeconomic status
Authors' response to: Childhood cancer and nuclear power plants in Switzerland: a census-based cohort study
Association between reported exposure to road traffic and respiratory symptoms in children: evidence of bias
Background Many studies showing effects of traffic-related air pollution on health rely on self-reported exposure, which may be inaccurate. We estimated the association between self-reported exposure to road traffic and respiratory symptoms in preschool children, and investigated whether the effect could have been caused by reporting bias. Methods In a random sample of 8700 preschool children in Leicestershire, UK, exposure to road traffic and respiratory symptoms were assessed by a postal questionnaire (response rate 80%). The association between traffic exposure and respiratory outcomes was assessed using unconditional logistic regression and conditional regression models (matching by postcode). Results Prevalence odds ratios (95% confidence intervals) for self-reported road traffic exposure, comparing the categories ‘moderate' and ‘dense', respectively, with ‘little or no' were for current wheezing: 1.26 (1.13-1.42) and 1.30 (1.09-1.55); chronic rhinitis: 1.18 (1.05-1.31) and 1.31 (1.11-1.56); night cough: 1.17 (1.04-1.32) and 1.36 (1.14-1.62); and bronchodilator use: 1.20 (1.04-1.38) and 1.18 (0.95-1.46). Matched analysis only comparing symptomatic and asymptomatic children living at the same postcode (thus exposed to similar road traffic) showed similar ORs, suggesting that parents of children with respiratory symptoms reported more road traffic than parents of asymptomatic children. Conclusions Our study suggests that reporting bias could explain some or even all the association between reported exposure to road traffic and disease. Over-reporting of exposure by only 10% of parents of symptomatic children would be sufficient to produce the effect sizes shown in this study. Future research should be based only on objective measurements of traffic exposur
Childhood leukaemia and socioeconomic status: what is the evidence?
The objectives of this systematic review are to summarise the current literature on socioeconomic status (SES) and the risk of childhood leukaemia, to highlight methodological problems and formulate recommendations for future research. Starting from the systematic review of Poole et al. (Socioeconomic status and childhood leukaemia: a review. Int. J. Epidemiol. 2006;35(2):370-384.), an electronic literature search was performed covering August 2002-April 2008. It showed that (1) the results are heterogeneous, with no clear evidence to support a relation between SES and childhood leukaemia; (2) a number of factors, most importantly selection bias, might explain inconsistencies between studies; (3) there is some support for an association between SES at birth (rather than later in childhood) and childhood leukaemia and (4) if there are any associations, these are weak, limited to the most extreme SES groups (the 10-20% most or least deprived). This makes it unlikely that they would act as strong confounders in research addressing associations between other exposures and childhood leukaemia. Future research should minimise case and control selection bias, distinguish between different SES measures and leukaemia subtypes and consider timing of exposures and cancer outcome
Breastfeeding and Respiratory Tract Infections during the First 2 Years of Life.
Breastfeeding protects against respiratory tract infections (RTIs) in infants [1–3], but whether its effects
persist beyond that age is not well understood. Some studies have reported that protection diminishes soon
after weaning [2], while others have found that it extends until the age of 2 years [4] or more [5, 6]. It is
noteworthy that many previous studies grouped RTIs broadly into upper or lower tract infections, rather
than studying specific diseases [3, 7], and few adjusted adequately for confounding factors [5] or
investigated a possible effect modification by sex, which had been suggested by several studies showing a
stronger protection in girls [8, 9].
This study aimed to quantify the protective effect of breastfeeding against RTIs during the first 2 years of
life, while adjusting for potential confounding factors and testing whether the effect varied by sex.
We analysed data from the Leicester Respiratory Cohorts, a population-based random sample of children
from Leicestershire, UK, which has been described in detail elsewhere [10]. For this analysis we included
only children born between 1996 and 1997 who were aged 1–1.99 years at the date of the first survey in
1998. Parents completed a standardised questionnaire that requested detailed information on breastfeeding
and respiratory symptoms. We assessed the duration of breastfeeding (no breastfeeding, ⩽6 months or
>6 months), the prevalence of frequent colds (>6 episodes), ear infections and croup within the last
12 months, and any episodes of bronchiolitis or pneumonia. We extracted perinatal data and demographic
information from maternity records. The Leicestershire Health Authority Research Ethics Committee
approved the study.
The survey requested information on a number of RTIs for each child, so we first performed an omnibus
logistic regression to determine whether breastfeeding was associated with the occurrence of any RTI. By
reforming the data into long format, this omnibus logistic regression also adjusted for the clustering of
observations within each child [11]. Following a significant omnibus test, we performed unadjusted and
adjusted logistic regressions to determine which RTIs were affected by breastfeeding practice. Adjusted
models controlled for sex, ethnicity, socioeconomic status (Townsend deprivation score [12]), perinatal
factors (gestational age, birthweight, birth season), environmental factors ( pre- and post-natal maternal
smoking, number of older siblings, day care attendance) and parental history of asthma, hay fever and
bronchitis. We tested for effect modification by sex by adding interaction terms into adjusted models.
Finally, we performed a sensitivity analysis including a subgroup of children with information on exact
breastfeeding duration, by using breastfeeding as a continuous exposure, rather than categorical. All
analyses were performed in Stata (version 14.2, Stata Corporation, Austin, TX, USA).
The survey in 1998 was sent to 5400 families with children aged between 1 and 1.99 years. Questionnaires
were returned by 4100 parents (response rate of 76%). After excluding 47 children who had no
breastfeeding information and 13 children born extremely prematurely (gestational age of <28 weeks [13]),
4040 children remained in the analysis. Of these, 52% were boys, 81% were white and 19% were of South
Asian ethnic origin, 1659 (41%) had never been breastfed, 1639 (41%) had been breastfed for ⩽6 months
and 742 (18%) for >6 months. Of the 4040 included children, 769 (19%) were reported by their parents to
have had frequent colds, 1685 (42%) ear infections and 293 (7%) croup within the last 12 months. Any
episodes of bronchiolitis were reported for 453 children (11%) and pneumonia for 53 (1%)Peer-reviewedPublisher Versio
Childhood cancer and nuclear power plants in Switzerland: a census-based cohort study
Background Previous studies on childhood cancer and nuclear power plants (NPPs) produced conflicting results. We used a cohort approach to examine whether residence near NPPs was associated with leukaemia or any childhood cancer in Switzerland. Methods We computed person-years at risk for children aged 0-15 years born in Switzerland from 1985 to 2009, based on the Swiss censuses 1990 and 2000 and identified cancer cases from the Swiss Childhood Cancer Registry. We geo-coded place of residence at birth and calculated incidence rate ratios (IRRs) with 95% confidence intervals (CIs) comparing the risk of cancer in children born 15 km away, using Poisson regression models. Results We included 2925 children diagnosed with cancer during 21 117 524 person-years of follow-up; 953 (32.6%) had leukaemia. Eight and 12 children diagnosed with leukaemia at ages 0-4 and 0-15 years, and 18 and 31 children diagnosed with any cancer were born 15 km away, the IRRs (95% CI) for leukaemia in 0-4 and 0-15 year olds were 1.20 (0.60-2.41) and 1.05 (0.60-1.86), respectively. For any cancer, corresponding IRRs were 0.97 (0.61-1.54) and 0.89 (0.63-1.27). There was no evidence of a dose-response relationship with distance (P > 0.30). Results were similar for residence at diagnosis and at birth, and when adjusted for potential confounders. Results from sensitivity analyses were consistent with main results. Conclusions This nationwide cohort study found little evidence of an association between residence near NPPs and the risk of leukaemia or any childhood cance
Validation of questionnaire-reported hearing with medical records: A report from the Swiss Childhood Cancer Survivor Study
BACKGROUND: Hearing loss is a potential late effect after childhood cancer. Questionnaires are often used to assess hearing in large cohorts of childhood cancer survivors and it is important to know if they can provide valid measures of hearing loss. We therefore assessed agreement and validity of questionnaire-reported hearing in childhood cancer survivors using medical records as reference.
PROCEDURE: In this validation study, we studied 361 survivors of childhood cancer from the Swiss Childhood Cancer Survivor Study (SCCSS) who had been diagnosed after 1989 and had been exposed to ototoxic cancer treatment. Questionnaire-reported hearing was compared to the information in medical records. Hearing loss was defined as ≥ grade 1 according to the SIOP Boston Ototoxicity Scale. We assessed agreement and validity of questionnaire-reported hearing overall and stratified by questionnaire respondents (survivor or parent), sociodemographic characteristics, time between follow-up and questionnaire and severity of hearing loss.
RESULTS: Questionnaire reports agreed with medical records in 85% of respondents (kappa 0.62), normal hearing was correctly assessed in 92% of those with normal hearing (n = 249), and hearing loss was correctly assessed in 69% of those with hearing loss (n = 112). Sensitivity of the questionnaires was 92%, 74%, and 39% for assessment of severe, moderate and mild bilateral hearing loss; and 50%, 33% and 10% for severe, moderate and mild unilateral hearing loss, respectively. Results did not differ by sociodemographic characteristics of the respondents, and survivor- and parent-reports were equally valid.
CONCLUSIONS: Questionnaires are a useful tool to assess hearing in large cohorts of childhood cancer survivors, but underestimate mild and unilateral hearing loss. Further research should investigate whether the addition of questions with higher sensitivity for mild degrees of hearing loss could improve the results
Physical performance limitations in adolescent and adult survivors of childhood cancer and their siblings.
PURPOSE: This study investigates physical performance limitations for sports and daily activities in recently diagnosed childhood cancer survivors and siblings.
METHODS: The Swiss Childhood Cancer Survivor Study sent a questionnaire to all survivors (≥ 16 years) registered in the Swiss Childhood Cancer Registry, who survived >5 years and were diagnosed 1976-2003 aged <16 years. Siblings received similar questionnaires. We assessed two types of physical performance limitations: 1) limitations in sports; 2) limitations in daily activities (using SF-36 physical function score). We compared results between survivors diagnosed before and after 1990 and determined predictors for both types of limitations by multivariable logistic regression.
RESULTS: The sample included 1038 survivors and 534 siblings. Overall, 96 survivors (9.5%) and 7 siblings (1.1%) reported a limitation in sports (Odds ratio 5.5, 95%CI 2.9-10.4, p<0.001), mainly caused by musculoskeletal and neurological problems. Findings were even more pronounced for children diagnosed more recently (OR 4.8, CI 2.4-9.6 and 8.3, CI 3.7-18.8 for those diagnosed <1990 and ≥ 1990, respectively; p=0.025). Mean physical function score for limitations in daily activities was 49.6 (CI 48.9-50.4) in survivors and 53.1 (CI 52.5-53.7) in siblings (p<0.001). Again, differences tended to be larger in children diagnosed more recently. Survivors of bone tumors, CNS tumors and retinoblastoma and children treated with radiotherapy were most strongly affected.
CONCLUSION: Survivors of childhood cancer, even those diagnosed recently and treated with modern protocols, remain at high risk for physical performance limitations. Treatment and follow-up care should include tailored interventions to mitigate these late effects in high-risk patients
- …
