Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Chronic health conditions and school performance in first graders: A prospective cohort study

  • Isabell Hoffmann,

    Roles Formal analysis, Methodology, Visualization, Writing – original draft

    Current address: Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Langenbeckstrasse 1, Mainz, Germany.

    Affiliation Division of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany

  • Christiane Diefenbach,

    Roles Conceptualization, Methodology

    Affiliation Division of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany

  • Christine Gräf,

    Roles Investigation, Methodology

    Affiliation Division of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany

  • Jochem König,

    Roles Methodology, Validation

    Affiliation Division of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany

  • Martina F. Schmidt,

    Roles Conceptualization, Investigation, Project administration

    Affiliation Division of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany

  • Kathleen Schnick-Vollmer,

    Roles Investigation, Methodology, Project administration

    Affiliation Division of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany

  • Maria Blettner,

    Roles Resources, Supervision, Writing – review & editing

    Affiliation Division of Epidemiological Methodology and Radiation Research, Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany

  • Michael S. Urschitz ,

    Roles Conceptualization, Funding acquisition, Methodology, Resources, Supervision, Writing – review & editing

    urschitz@uni-mainz.de

    Affiliation Division of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology, and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany

  • for the ikidS Study Group

    Membership of the ikidS Study Group is listed in the Acknowledgments.

Chronic health conditions and school performance in first graders: A prospective cohort study

  • Isabell Hoffmann, 
  • Christiane Diefenbach, 
  • Christine Gräf, 
  • Jochem König, 
  • Martina F. Schmidt, 
  • Kathleen Schnick-Vollmer, 
  • Maria Blettner, 
  • Michael S. Urschitz, 
  • for the ikidS Study Group
PLOS
x

Abstract

Objective

Children with chronic health conditions may perform poorer at school. Associations may be confounded by numerous social factors. We aimed to estimate the effects of a chronic health condition on overall school performance in first graders with an emphasis on rigorous adjustment for potential confounders.

Methods

A population-based cohort study was performed in the area of Mainz-Bingen (Germany). In 2015 all preschoolers were approached and the presence of a chronic health condition was assessed by parental questionnaires and preschool health examination data. The identification of a chronic health condition was based on special health care needs and presence of a doctor’s diagnosis out of 24 school-relevant diseases. At the end of the first school year, overall school performance was assessed by teachers and rated on a 5-item scale ranging from -10 to +10.

Results

Of 3683 children approached, 2003 were enrolled. Overall school performance was available for 1462 children (51% boys). Of these, 52% suffered from a chronic health condition. Compared to children without a chronic health condition, children with special health care needs (15%) performed worse at school (adjusted mean difference: -0.95, 95% CI: [-1.55; -0.35], P = 0.002). Children with a doctor’s diagnosis but without special health care needs (37%) did not perform worse at school. The effect was further analysed considering the extent of special health care needed.

Conclusions

Chronic health conditions affect overall school performance early in primary school. To identify academically at-risk children, a chronic health condition identification based on special health care needs may be used.

Introduction

There are many reasons that children underperform at school, including a poor socio-cultural (home) environment, specific learning disabilities, and in particular chronic health conditions (CHC). Since 2005, several systematic reviews have investigated and evaluated the growing body of evidence in this field [14]. In 2011, Suhrcke and de Paz Nieves were the first to propose a theoretical framework for the relationship between CHC and educational outcomes [5]. They differentiated between short- (i.e. academic performance) and long-term (i.e. educational attainment) outcomes, proposed potential mediating factors and confounders, and presented cross-sectional and longitudinal evidence for the relationship. Dadaczynski was the first to include only longitudinal studies to reach a higher level of causal inference in his systematic review [6]. He pointed out that adequately designed and analysed longitudinal studies are lacking. In summary, these reviews provided supportive evidence that CHC such as asthma, obesity, sleep disorders, and mental health disorders (i.e. anxiety, depression, behavioural disturbances, and attention-deficit hyperactivity disorder) may have a negative impact on educational outcomes. The authors underlined the importance of appropriate adjustment for confounding factors such as socio-economic status and pointed out that the level and quality of health care prior to school entry as well as the extent and effectiveness of special educational support have not been sufficiently investigated in most studies [5, 6]. However, this is important to understand regional differences in the effects of CHC on educational outcomes and to identify ameliorating effects of health care interventions and special educational support on educational outcomes.

There is a large debate on the appropriate framework of CHC in childhood [7]. The identification of a CHC can be based on either a specific doctor’s diagnosis of a chronic disease (i.e. diagnosis-based framework) or the need for special health care services (i.e. consequence-based framework). The diagnosis-based framework is grounded in the ICD classification, the availability of valid methods for the diagnosis, a non-curability of the disease, and the actual or expected duration of the disease [8]. The consequence-based framework is usually operationalised in short parental screening questionnaires such as the Children with Special Health Care Needs (CSHCN) Screener [9]. This instrument is increasingly used in national and international studies on epidemiological aspects of CHC in childhood [1012]. However, studies combining both frameworks are lacking. In particular, it is unclear which framework should be used to identify academically at-risk children prior to school entry.

We, hence, initiated the ikidS project (ikidS: ich komme in die Schule [German]; I am starting school) in 2013 as the first large cohort study in Germany investigating long-term outcomes of CHC in primary schoolchildren. The project combined both frameworks of CHC, investigated outcomes in the domains mental health, quality of life, social participation, and school performance, and assessed the use of health care services as well as special educational support. In the present report, we aimed to estimate the effects of CHC on 1st grade overall school performance (OSP) in combining both frameworks of CHC and with rigorous adjustments for potential confounders.

Methods

Study region, setting, and design

A prospective, population-based, closed cohort study was performed between September 2014 and September 2016 within the city of Mainz and the district of Mainz-Bingen (Federal State of Rhineland-Palatinate; Germany), which covers an area of 704 square kilometres with a population of 418,528 inhabitants. In 2015, there were 79 public and private primary and special needs schools located in this area, and 3,683 children were officially registered for their first year of school. The research protocol was approved by the ethics committee of the regional medical association of Rhineland-Palatinate, the regional supervisory school authority, and the state representative for data protection in Rhineland-Palatinate.

Study population, enrolment, and study sample

The study population consisted of all children who had their preschool health examination (PHE) within the study region between September 1st, 2014, and August 31st, 2015. The PHE is a standardised, compulsory, state-wide health examination performed by public youth health physicians employed by the regional Department of Public Health of the Mainz-Bingen District. Participants were enrolled on the day of the PHE by a public youth health physician and parental informed written consent was obtained. For the present work, children, who i) ultimately did not enter school in September 2015, ii) were assigned to a special needs school or iii) had no results for 1st grade OSP were later excluded from the analysis.

Procedures and data collection

Data were collected at four time points: at the PHE during the last preschool year (T0), six weeks before school entry (T1), three months after school entry (T2), and at the end of 1st grade (T3). The PHE comprised a statutory parental questionnaire (including information on parental education and migrant background), a thorough medical history and physical examination, and the administration of screening tests as well as tests on pre-academic skills. At time points T1 to T3, general and mental health, presence of CHC, need for and use of special health care, family structure and burden, leisure time activities, nutritional habits, environmental conditions, and socio-economic status were assessed by using study-specific parental questionnaires, respectively.

Identification of children with CHC

The identification of children with CHC based on both the consequence-based and the diagnosis-based framework. For the consequence-based approach, children with actual needs for special health care services were identified by a German version of the CSHCN Screener [9]. The CSHCN Screener is a 14-item parent-reported instrument covering five aspects (or indicators) of medical care: (1) need for prescription medication, (2) need for social or educational support, (3) functional limitations, (4) need for physical, occupational, or speech therapy, and (5) mental health problems. Each aspect has one key question with one or two additional questions, which assess whether the condition is due to a medical or other health condition and whether the duration or expected duration of the condition is 12 months or longer. The Screener indicates a CHC if the key question and its accompanying question(s) are answered positively for at least one of the five aspects. Validity and performance of the Screener have been investigated in children with disabilities [9] and diagnoses of chronic conditions made by a physician [11] as well as with respect to other parental screening instruments [13]. The Screener has been used in nation-wide health surveys in the US [14] and Germany [10]. In the present study, the CSHCN Screener was administered at time points T1 to T3.

Regarding the diagnosis-based approach, PHE data and study-specific parental questionnaires were evaluated at time points T0 to T3 for the presence (“ever”, “during the last 12 months” or “currently”) of one of the following 24 doctors’ diagnoses or chronic conditions: anaemia, asthma, atopic dermatitis, attention-deficit hyperactivity disorder, autism, conduct disorder, emotional problems, depression, diabetes mellitus, dwarfism, epilepsy, heart defect, hay fever, hearing impairment, hypothyreosis, low birthweight, overweight/obesity, premature birth, sleepiness, snoring, speech and language disorder, tumour/cancer, being underweight, and visual impairment. For these diagnoses and conditions, associations with educational outcomes have been demonstrated in previous studies [1, 5, 1530]. A detailed description of how these diagnoses and conditions were identified is given in S1 Table.

Educational outcomes

OSP was defined in accordance with the German National Educational Panel Study [31]. Teachers were asked to rate the child’s abilities in reading, writing, numeracy, science, and in social competencies in comparison to their peers of same age, each on a 5-point rating scale ranging from “much lower than average” and “lower than average” to “in average”, “higher than average” and “much higher than average”. Arbitrary numerical scores were assigned to each response category (i.e. -2, -1, 0, +1 and +2, respectively). Item scores were summed to obtain a combined OSP score ranging from -10 to +10, with 0 indicating average performance.

Statistical methods

After enrolment of the study participants, representativeness of the sample was assessed by comparing important health and socio-demographic characteristics between the study sample and the source population. Anonymous PHE data provided by the Department of Public Health were analysed using appropriate statistical parameters (e.g. numbers and frequencies for categorical variables, and mean and standard deviation (SD) for normally distributed variables).

For the primary analysis, the exposure variable was CHC as defined in Table 1. In terms of simpler legibility, we call the reference group “no CHC”, even though there may still be children with special health care needs and/or doctors’ diagnoses. The primary outcome was OSP score. Potential confounders were identified following the causal model of Suhrcke and Paz Nieves [5] and an extensive literature search. Confounder variables were only included in the regression analysis if they were empirically associated in our data with both, exposure and outcome variables. The following confounders were ultimately included: socio-economic status, gender, migrant background, single parent family, multiple births (e.g. twins), breast feeding, household smoking, life style and leisure time activities (e.g. active and interactive behaviour, outdoor activities, early musical education, television in the child’s bedroom), and location of the school (see S2 Table). The following factors did not show an association with OSP and where not included in the model: single child, nutritional habits, CHC of a family member, and age at school entry.

thumbnail
Table 1. Definition of chronic health conditions (CHC) and frequencies within the study sample (N = 1462).

https://doi.org/10.1371/journal.pone.0194846.t001

The amount of missing values ranged from a very low frequency in variables assessed by PHE (e.g. gender: 0%, doctor’s diagnosis: 0%, smoking in household: 3%) up to 40% in variables assessed by study-specific parental questionnaires (e.g. early musical education: 20%, special health care needs: 22%, leisure time activities: 27%, socio-economic status: 40%). Missing values of the CSHCN Screener items and all confounders were imputed 10 times using chained equations with 100 iterations [32]. For each imputed variable, an individual set of variables was used as predictor variables. Missing values for OSP score were imputed using chained equations, if only one or two items of the OSP score were missing. In this case, the available OSP items were used as predictor variables. The effect of CHC on OSP was modelled using linear mixed-effects regression models with a random effect for school class and adjusted for the covariates mentioned above (M1). The results of the model are shown as effect estimates of CHC with 95% confidence intervals and P values. Results were also presented as least-means squares (marginal means) with confidence intervals for CHC stratified by gender.

As a secondary analysis, the relationship between special health care needs and OSP was further investigated by estimating the effects of each of the five individual indicators of the CSHCN Screener (M2), and the total sum of these positively answered indicators (M3) on OSP. For this analysis, a linear mixed-effects model with the same covariates and random effect for school class was used as in the primary analysis. The analysis was performed using the software packages R (version 3.4.1), nlme (version 3.1–131), and mice (version 2.30) [33] and the S1 Public Use File.

Results

Study participants and sample

Of 3683 eligible children, 2003 (i.e. study participants, 54% of the study population) were enrolled. Responses of parental questionnaires ranged from 1454 at T1 to 1230 at T3, and 1524 children were assessed by teachers (Fig 1). Finally, diagnoses and OSP data were available for 1462 children (i.e. study sample, 40% of the study population; Fig 1). Except for migrant background (20.7% vs. 22.3%), the study sample was fully representative of the underlying study population (Table 2). However, outbalancing this deviation by using population-based sampling weights in the analysis (i.e. weighted regression) did not change results. Hence, data are not shown.

thumbnail
Fig 1. Flow-chart for the participants of ikidS, showing response rates of parental questionnaires, teachers’ and children’s assessments.

https://doi.org/10.1371/journal.pone.0194846.g001

thumbnail
Table 2. Characteristics of children within the study region (population), children enrolled into the study (participants), and children with available school performance data (sample).

Unless otherwise stated, characteristics are summarised by total numbers (N) and frequencies (%).

https://doi.org/10.1371/journal.pone.0194846.t002

Information on doctors’ diagnoses was available for all study participants. The frequencies of the 24 diagnoses/chronic conditions under study are given in S1 Table. Of these, premature birth (N = 133), sleepiness (N = 119), atopic dermatitis (N = 113), asthma (N = 103), and being underweight (N = 84) were the most frequent CHC (S1 Table).

CSHCN Screener information was available for 1145 children (31% of the study population). Of these, 52% fulfilled at least one of the two criteria for CHC, whereby 15% were children with special health care needs, 45% had one out of the 24 diagnoses/conditions under study, and 37% had a diagnosis/condition but no special health care needs (Table 1). Need or use of prescription medication for an ongoing condition was the Screener criterion most frequently met by the children (N = 81; 6.9%), followed by above-routine use of health or related services (N = 79; 6.8), and treatment or counselling for an emotional, developmental, or behavioural problem (N = 72; 6.2%; S4 Table).

Chronic health condition and overall school performance

Children with any kind of CHC had lower OSP scores (mean = 1.3; SD = 3.8) compared to children without CHC (mean = 2.1; SD = 3.4). Children with missing values for special health care needs (N = 317; 22% of the study sample) had an even lower OSP score (mean = -1.3, SD = 3.7), which demonstrated the need for imputing missing values for special health care needs. More information about the characteristics of the three CHC groups are given in S3 Table.

After imputing missing values and adjusting for potential confounders, children with special health care needs performed worse compared to children with no CHC (M1: adjusted OSP mean difference: -0.95, 95% CI [-1.55, -0.35], P = 0.002; Table 3). Children with one out of the 24 diagnoses under study but no special health care needs did not perform worse (M1 adjusted mean difference: -0.02, 95% CI [-0.38, 0.42], P = 0.98; Table 3). Fig 2 demonstrates the lower marginal means in OSP for children with special health care needs in comparison to the other CHC groups.

thumbnail
Table 3. Analysis of chronic health condition on overall school performance.

The effect of chronic health conditions (M1), the effect of each indicator of the CSHCN Screener (M2) and the numbers of qualifying indicators of the CSHCN Screener (M3) on overall school performance as assessed by multivariable linear regression analysis (N = 1462).

https://doi.org/10.1371/journal.pone.0194846.t003

Indicators of the CSHCN Screener and OSP

The needs for special health care services was defined by 5 different indicators of the CSHCN Screener (S4 Table). Use of prescription medications (6.9% of those with available CSHCN Screener information) and above-average need for medical, mental health, or educational services (6.8% of those with available CSHCN Screener information) were the most common needs in the study sample.

In a secondary analysis, none of the single indicators of the CSHCN Screener showed a clear association with OSP (M2 in Table 3. However, if more than one indicator was fulfilled (7.2% of those with available CSHCN Screener information), OSP was markedly lower compared to children without CHC (M3: adjusted mean difference: -1.51, 95% CI [-2.36,-0.65], P < 0.001; Table 3).

Discussion

In the present study, the presence of CHC at school entry was independently associated with OSP at the end of first grade. The association was clearly seen for children with increased needs of special health care and remained after adjusting for a series of potential confounders. Moreover, the observed effect was stronger in children, who had more than one indicator of special health care needs. To our knowledge, this is the first European study on this topic in primary schoolchildren, thereby compensating for the geographical bias in the research, which has been mentioned previously [5]. The data may now be used to further explore how investments in health care services could improve educational outcomes.

Our results are in line with previous studies in children and adolescents utilizing parental reports of special health care needs [34, 35], chronic illness [36], and doctors’ diagnoses of CHC [37, 38] as well as electronic health records of general practitioners as data sources of child health [39]. In contrast to these studies, we used two different and independent frameworks of CHC (i.e. diagnosis- and consequence-based) at the same time. In a previous study, the diagnosis-based framework yielded 285 different ICD diagnoses or clusters of diagnoses that fulfilled requirements for CHC [8]. However, in a public health setting (such as the PHE) it is not feasible to access such a large number of diagnoses. Instead, we restricted our assessment to diseases, which were frequent and relevant for school enrolment, management at school, and/or school performance. As a result, the presence of one out of 24 doctors’ diagnoses without increased special health care needs was not associated with OSP. This may question the benefit of generally assessing doctors’ diagnoses in the PHE. A low concurrence between parental reports and medical records in less educated parents further weakens the diagnosis-based framework for studies aiming at educational outcomes [40].

We found information of the CSHCN Screener independently associated with OSP. Children with two or more qualifying indicators of the instrument performed especially worse at school. This is in line with previous studies, where CSHCN Screener items and/or profiles were associated with educational outcomes such as school attendance, grade point average, special education needs, grade repetition, and lack of school engagement [34, 35]. Our results extend these observations and showed clear benefits of adding the CSHCN Screener to PHE. According to our results, this short instrument may be sufficiently accurate to identify an academically at-risk group of children prior to school entry. This may further replace parent reports of a doctor’s diagnosis in future developments of PHE.

Many studies have evaluated the association between one type or one group of CHC and educational outcomes [3, 5, 6, 41]. However, the cause-effect relationship between CHC and educational outcomes remains still unclear due to insufficient samples, inappropriate adjustments, and other methodological shortcomings in some studies [5]. There are likely many predictor variables, mediators and modifiers for educational outcomes in children and residual confounding remains a great threat to observational studies such as the present. Thus, we applied and extended an analytical framework for the relationship between health and education in high-income countries and for the selection of potential confounders [5]. They were evaluated for their association with CHC and OSP, and were finally included in the statistical models. Apart from socio-economic status and having a migrant background, we identified important family- and leisure time-related confounders. However, it is still possible that there is a third factor that explains the association.

In our study, the frequency of CHC ranged from 15% to 45% depending on the definition used (i.e. consequence- or diagnosis-based). There is a large range of definitions and operationalisations for CHC in childhood [7]. This leads to a wide variability in prevalence estimates, ranging from 0.2% to 44% [7]. Concerning the consequence-based definition, our results (15%) were in accordance with representative survey data from the German KIGGS study and the 2003 US National Survey of Children’s Health, which found prevalence estimates ranging from 13.7% to 17.6% [10, 12]. Concerning the diagnosis-based definition, our results (45%) were slightly higher compared to the KIGGS study (38.7%), which used a list of 17 common doctors’ diagnoses for the definition of CHC [42], and the Canadian Longitudinal Survey of Children and Youth (30.3%; [43]). The higher frequency in the present study could be explained by some items in the statutory parental PHE questionnaire that evaluated the presence of doctors’ diagnoses with a life-time perspective (i.e., items asked for “ever” having had a specific diagnosis). This has likely enlarged the group of children with any CHC but enabled us to form a largely “disease-free” reference group for unbiased estimations of CHC effects.

Several limitations should be mentioned. Early OSP was assessed by teacher reports at the end of first grade. As grades are not assigned to first and second grade pupils in Rhineland-Palatinate and objective and standardised school performance tests are not routinely performed in this age group, we used an established instrument from the German National Educational Panel Study to evaluate a broad range of school-related competencies. However, teacher ratings may be subjective to their occupational experience, their attitude towards a child, and the mean level of competencies within the whole class. The resulting clustering in the outcome variable has been accounted for in the analysis by adding a random intercept for teacher/class in the models.

The diagnosis-based approach was based on a list of doctors’ diagnoses, which were in the focus of the statutory PHE because these CHC were related to poor OSP in previous studies. However, the selection was more or less arbitrary and disease severity was not obtained. Hence, we might have neglected potentially important diseases that might have been relevant for OSP. In fact, CHC consist of a very diverse set of diagnoses. In the present study, we did not divide the conditions up in the analysis, because this would go far beyond the scope of the present publication. However, a breakdown of the CHC groups into different groups of diagnoses may well have shown vastly different results. Further analyses comparing mental CHC with physical CHC are currently underway and will enlighten the relative relevance of CHC groups in terms of educational outcomes. Until further results are available, we recommend focussing on those children who already have special health care needs according to the CSHCN Screener, independent of their specific diagnosis.

The consequence-based approach was based on the CSHCN Screener, a short, feasible, and efficient screening instrument developed to identify children with chronic conditions for a variety of purposes, including public health monitoring, health care quality assessment, and programme planning and evaluation [9]. The performance of the Screener varies depending on the setting and chronic condition. In a sample of children enrolled in the US Medicaid managed care health plans, 53% of children were screened as positive whereas in a sample of children receiving supplemental income for disability, 94% of children were correctly identified with special health care needs [9]. In two validation studies, sensitivity ranged from 69% for skin diseases to 91% for epilepsy [11], and the positive and negative predictive values were determined to be 93% and 89%, respectively [13]. However, children with CHC may not be identified as such as they do not meet the criteria of this Screener in every case [11]. Although the instrument is well established and frequently used in large surveys [10, 14], the precise accuracy of the instrument remains unknown, and due to its nature it is–at least to some extend—subject to misclassification.

There is vast variability within the category of CSHCN. Most children qualified for CSHCN due to a medication prescription (CSHCN indicator 1) or above-average use of medical care, mental health, or educational services (CSHCN indicator 2). The use of educational services is a marker of poor school performance and it would be not surprising that these children do not perform as well in school. However, only six out of 171 children were positively screened due to CSHCN indicator 2 at the end of the first grade. Excluding these children from the analysis did not change the effect estimates decisively. Thus, all children meeting the criteria of the CSHCN indicator 2 had in fact only above-average use of medical care or mental health services.

Missing values up to 40% of cases was an issue in this study, which can be a source of bias for effect estimates. In order to cope with that, missing values were imputed prior to regression analysis, which is an adequate method for dealing with values missing at random in longitudinal studies [44]. Although children with missing CSHCN Screener information had lower mean OSP values compared to children with available information, a complete case analysis resulted in the same effect estimates for CHC. The same source of bias was identified for socio-economic status. Hence, only effect estimates after imputation are presented in this work. This enabled us to present largely unbiased estimates of the association between CHC and OSP in young primary school children.

Conclusions

The presence of CHC at school entry may have negative effects on OSP at the end of first grade. A consequence-based approach, such as using the CSHCN Screener, can identify a group of children with CHC who may be particularly at risk for performing worse at school. Whether these children may benefit from early targeted medical, educational, and/or social support interventions should be addressed in the future. Long-term follow-up of future school performance is highly desirable in children with CHC to estimate the burden on this population at-risk.

Supporting information

S1 Table. Overview of the identification of diagnoses and conditions of chronic health conditions.

If one of the questions was answered positively by parents, the child was assumed to have a diagnosis for this disease.

https://doi.org/10.1371/journal.pone.0194846.s001

(PNG)

S2 Table. Overview of how confounders were defined using the information from parental questionnaires.

Confounders were used for the analysis of the effect of chronic health conditions on overall school performance.

https://doi.org/10.1371/journal.pone.0194846.s002

(PNG)

S3 Table. Characteristics of children within each group of chronic health condition.

Characteristics of children with special health care needs (alone or in combination with a doctor’s diagnosis/condition), children with a diagnosis of a chronic disease (only), and children with no chronic health condition.

https://doi.org/10.1371/journal.pone.0194846.s003

(PNG)

S4 Table. Frequencies of children with different characteristics for special health care needs.

Frequencies of children with special health care needs, its individual indicators, and the number of qualifying indicators of the CSHCN1 Screener (N = 1145, missings not shown).

https://doi.org/10.1371/journal.pone.0194846.s004

(PNG)

S1 Public Use File. The public use file consists of the following variables used in primary analysis: Socioeconomic status (socEcoStat), gender, overall school performance (osp), migration background (mig), one-parent family (oneParFam), school location urban/rural, (location), breastfeeding (breastfeed), active and interactive behaviour (actInterBeh), early musical education (musicEdu), television in child room (tvChildroom), outdoor activities (outdoor), smoking in house hold (smokingHH), multiples (multiples), school class (schoolClass), chronic health condition (chc).

https://doi.org/10.1371/journal.pone.0194846.s005

(TXT)

Acknowledgments

Our thanks go to the documentation specialists and student research aids for conducting the surveys at school. Grateful acknowledgment goes to Katherine Taylor for proofreading. Last but not least, we particularly wish to thank all the parents and children for their patience and cooperation; they made this study possible. We can provide the prediction matrix used in the imputation procedure or the resulting R object upon request.

IkidS study team

Dietmar Hoffmann (Department of Public Health, County Government Mainz-Bingen), Maria Blettner, Peter Kaatsch (Institute of Medical Biostatistics, Epidemiology, and Informatics; University Medical Center of the Johannes Gutenberg-University Mainz), Annette Queisser-Wahrendorf, Awi Wiesel, Fred Zepp, Jörg Faber, Stephan Gehring, Eva Mildenberger (Department of Pediatrics; University Medical Center of the Johannes Gutenberg-University Mainz), Michael Huss (Department of Child and Adolescence Psychiatry; University Medical Center of the Johannes Gutenberg-University Mainz), Stephan Letzel (Institute of Occupational, Social and Environmental Medicine; University Medical Center of the Johannes Gutenberg-University Mainz), Heike Elflein, Alexander Schuster (Department of Ophthalmology, University Medical Center of the Johannes Gutenberg-University Mainz), Brita Willershausen, Jens Weusmann (Department of Prosthodontics, University Medical Center of the Johannes Gutenberg-University Mainz), Christoph Matthias (Department of Communication Disorders; University Medical Center of the Johannes Gutenberg-University Mainz), Margarete Imhof (Department of Educational Psychology, Johannes Gutenberg-University Mainz), and Perikles Simon (Department of Sports Medicine, Johannes Gutenberg-University Mainz).

References

  1. 1. Taras H, Potts-Datema W. Childhood asthma and student performance at school. The Journal of school health. 2005;75(8):296–312. Epub 2005/09/24. pmid:16179080.
  2. 2. Taras H, Potts-Datema W. Obesity and student performance at school. The Journal of school health. 2005;75(8):291–5. Epub 2005/09/24. pmid:16179079.
  3. 3. Taras H, Potts-Datema W. Chronic health conditions and student performance at school. The Journal of school health. 2005;75(7):255–66. Epub 2005/08/17. pmid:16102088.
  4. 4. Taras H, Potts-Datema W. Sleep and student performance at school. The Journal of school health. 2005;75(7):248–54. Epub 2005/08/17. pmid:16102087.
  5. 5. Suhrcke M, de Paz Nieves C. The impact of health and health behaviours on educational outcomes in highincome countries: a review of the evidence2011.
  6. 6. Dadaczynski K. Stand der Forschung zum Zusammenhang von Gesundheit und Bildung. Überblick und Implikationen für die schulische Gesundheitsförderung. Zeitschrift für Gesundheitspsychologie. 2012;20(3):141–53.
  7. 7. van der Lee JH, Mokkink LB, Grootenhuis MA, Heymans HS, Offringa M. Definitions and measurement of chronic health conditions in childhood: a systematic review. Jama. 2007;297(24):2741–51. pmid:17595275
  8. 8. Mokkink LB, Van der Lee JH, Grootenhuis MA, Offringa M, Heymans HS. Defining chronic diseases and health conditions in childhood (0–18 years of age): national consensus in the Netherlands. European Journal of Pediatrics. 2008;167(12):1441–7. pmid:18340463
  9. 9. Bethell CD, Read D, Stein RE, Blumberg SJ, Wells N, Newacheck PW. Identifying children with special health care needs: development and evaluation of a short screening instrument. Ambulatory pediatrics: the official journal of the Ambulatory Pediatric Association. 2002;2(1):38–48. pmid:11888437.
  10. 10. Scheidt-Nave C, Ellert U, Thyen U, Schlaud M. [Prevalence and characteristics of children and youth with special health care needs (CSHCN) in the German Health Interview and Examination Survey for Children and Adolescents (KiGGS)]. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz. 2007;50(5–6):750–6. Epub 2007/05/22. pmid:17514460.
  11. 11. Schmidt S, Thyen U, Petersen C, Bullinger M. The performance of the screener to identify children with special health care needs in a European sample of children with chronic conditions. Eur J Pediatr. 2004;163(9):517–23. Epub 2004/08/24. pmid:15322869.
  12. 12. Bethell CD, Read D, Blumberg SJ, Newacheck PW. What is the prevalence of children with special health care needs? Toward an understanding of variations in findings and methods across three national surveys. Matern Child Health J. 2008;12(1):1–14. pmid:17566855.
  13. 13. Bethell CD, Read D, Neff J, Blumberg SJ, Stein RE, Sharp V, et al. Comparison of the children with special health care needs screener to the questionnaire for identifying children with chronic conditions—revised. Ambulatory pediatrics: the official journal of the Ambulatory Pediatric Association. 2002;2(1):49–57. Epub 2002/03/13. pmid:11888438.
  14. 14. Blumberg SJ, Welch EM, Chowdhury SR, Upchurch HL, Parker EK, Skalland BJ. Design and operation of the National Survey of Children with Special Health Care Needs, 2005–2006. Vital and health statistics Ser 1, Programs and collection procedures. 2008;(45):1–188. Epub 2009/03/17. pmid:19284158.
  15. 15. O'Connell EJ. The burden of atopy and asthma in children. Allergy. 2004;59 Suppl 78:7–11. Epub 2004/07/13. pmid:15245350.
  16. 16. Polderman TJC, Boomsma DI, Bartels M, Verhulst FC, Huizink AC. A systematic review of prospective studies on attention problems and academic achievement. Acta Psychiatrica Scandinavica. 2010;122(4):271–84. pmid:20491715
  17. 17. Troyb E, Orinstein A, Tyson K, Helt M, Eigsti IM, Stevens M, et al. Academic abilities in children and adolescents with a history of autism spectrum disorders who have achieved optimal outcomes. Autism. 2014;18(3):233–43. Epub 2013/10/08. pmid:24096312; PubMed Central PMCID: PMCPMC4481875.
  18. 18. Esch P, Bocquet V, Pull C, Couffignal S, Lehnert T, Graas M, et al. The downward spiral of mental disorders and educational attainment: a systematic review on early school leaving. BMC Psychiatry. 2014;14(1):237. pmid:25159271
  19. 19. Stabler B, Clopper RR, Siegel PT, Stoppani C, Compton PG, Underwood LE. Academic achievement and psychological adjustment in short children. The National Cooperative Growth Study. J Dev Behav Pediatr. 1994;15(1):1–6. Epub 1994/02/01. pmid:8195431.
  20. 20. Wright M, Nolan T. Impact of cyanotic heart disease on school performance. Arch Dis Child. 1994;71(1):64–70. pmid:8067795.
  21. 21. Blaiss MS. Allergic rhinitis and impairment issues in schoolchildren: a consensus report. Current medical research and opinion. 2004;20(12):1937–52. Epub 2005/02/12. pmid:15704310.
  22. 22. Cohen AK, Rai M, Rehkopf DH, Abrams B. Educational attainment and obesity: a systematic review. Obesity reviews: an official journal of the International Association for the Study of Obesity. 2013;14(12):989–1005. Epub 2013/07/31. pmid:23889851; PubMed Central PMCID: PMCPMC3902051.
  23. 23. Lieu JE, Tye-Murray N, Fu Q. Longitudinal study of children with unilateral hearing loss. Laryngoscope. 2012;122(9):2088–95. Epub 2012/08/07. pmid:22865630; PubMed Central PMCID: PMCPMC3467198.
  24. 24. Leger J, Larroque B, Norton J. Influence of severity of congenital hypothyroidism and adequacy of treatment on school achievement in young adolescents: a population-based cohort study. Acta Paediatr. 2001;90(11):1249–56. Epub 2002/01/26. pmid:11808894.
  25. 25. Bettge S, Oberwohrmann S, Brockstedt M, Buhrer C. Birth weight and special educational needs: results of a population-based study in Berlin. Dtsch Arztebl Int. 2014;111(19):337–44. pmid:24875458; PubMed Central PMCID: PMC4039004.
  26. 26. Moreira RS, Magalhaes LC, Alves CR. Effect of preterm birth on motor development, behavior, and school performance of school-age children: a systematic review. Jornal de pediatria. 2014;90(2):119–34. Epub 2013/12/29. pmid:24370176.
  27. 27. Urschitz MS, Eitner S, Guenther A, Eggebrecht E, Wolff J, Urschitz-Duprat PM, et al. Habitual snoring, intermittent hypoxia, and impaired behavior in primary school children. Pediatrics. 2004;114(4):1041–8. pmid:15466103.
  28. 28. Stoeckel RE, Colligan RC, Barbaresi WJ, Weaver AL, Killian JM, Katusic SK. Early speech-language impairment and risk for written language disorder: a population-based study. J Dev Behav Pediatr. 2013;34(1):38–44. Epub 2013/01/01. pmid:23275057; PubMed Central PMCID: PMCPMC3546529.
  29. 29. Gurney JG, Krull KR, Kadan-Lottick N, Nicholson HS, Nathan PC, Zebrack B, et al. Social outcomes in the Childhood Cancer Survivor Study cohort. J Clin Oncol. 2009;27(14):2390–5. Epub 2009/02/20. pmid:19224833; PubMed Central PMCID: PMCPMC2677924.
  30. 30. Kaestner R, Grossman M. Effects of weight on children's educational achievement. Economics of Education Review. 2009;28(6):651–61.
  31. 31. Blossfeld H-P, Maurice J, Schneider T. The National Educational Panel Study: need, main features, and research potential. Zeitschrift für Erziehungswissenschaft. 2011;14(2):5–17.
  32. 32. van Buuren S, Groothuis-Oudshoorn K. mice: Multivariate Imputation by Chained Equations in R. Journal of Statistical Software. 2011;45(3).
  33. 33. R-Core-Team. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing. 2017.
  34. 34. Forrest CB, Bevans KB, Riley AW, Crespo R, Louis TA. School outcomes of children with special health care needs. Pediatrics. 2011;128(2):303–12. pmid:21788226; PubMed Central PMCID: PMCPMC3387854.
  35. 35. Reuben CA, Pastor PN. The effect of special health care needs and health status on school functioning. Disability and Health Journal. 2013;6(4):325–32. http://dx.doi.org/10.1016/j.dhjo.2013.03.003. pmid:24060255
  36. 36. Quach J, Barnett T. Impact of chronic illness timing and persistence at school entry on child and parent outcomes: Australian longitudinal study. Acad Pediatr. 2015;15(1):89–95. Epub 2014/12/03. pmid:25444652.
  37. 37. Crump C, Rivera D, London R, Landau M, Erlendson B, Rodriguez E. Chronic health conditions and school performance among children and youth. Annals of Epidemiology. 2013;23(4):179–84. http://dx.doi.org/10.1016/j.annepidem.2013.01.001. pmid:23415278
  38. 38. Martinez YJ, Ercikan K. Chronic illnesses in Canadian children: what is the effect of illness on academic achievement, and anxiety and emotional disorders? Child Care Health Dev. 2009;35(3):391–401. pmid:19397602.
  39. 39. Uiters E, Maurits E, Droomers M, Zwaanswijk M, Verheij RA, van der Lucht F. The association between adolescents’ health and disparities in school career: a longitudinal cohort study. BMC Public Health. 2014;14:1104. PMC4216913. pmid:25344832
  40. 40. Miller JE, Gaboda D, Davis D, Centers for Disease C, Prevention/National Center for Health S. Early childhood chronic illness: comparability of maternal reports and medical records. Vital Health Stat 2. 2001;(131):1–10. pmid:15791760.
  41. 41. Currie J. Healthy, wealthy and wise: socioeconomic status, poor health in childhood and human capital development. National Bureau of Economic Research, Cambridge, MA, Working Paper No 1398. 2008.
  42. 42. Scheidt-Nave C, Ellert U, Thyen U, Schlaud M. [Health care needs of children and adolescents with chronic conditions]. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz. 2008;51(6):592–601. pmid:18465101.
  43. 43. McDougall J, King G, de Wit DJ, Miller LT, Hong S, Offord DR, et al. Chronic physical health conditions and disability among Canadian school-aged children: a national profile. Disability and rehabilitation. 2004;26(1):35–45. pmid:14660197.
  44. 44. De Silva AP, Moreno-Betancur M, De Livera AM, Lee KJ, Sompson JA. A comparison of multiple imputation methods for handling missing values in longitudinal data in presence of a time-varying covariate with a non-linear association with time: a simulation study. BMC medical research methodology. 2017;17(114).