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BRIEF RESEARCH REPORT article

Front. Nutr., 01 March 2024
Sec. Nutrition Methodology
Volume 11 - 2024 | https://doi.org/10.3389/fnut.2024.1279931

Agreement between parent-report and EMR height, weight, and BMI among rural children

  • Center for Obesity and Metabolic Research, Geisinger Health System, Danville, PA, United States

Introduction: Remote anthropometric surveillance has emerged as a strategy to accommodate lapses in growth monitoring for pediatricians during coronavirus disease 2019 (COVID-19). The purpose of this investigation was to validate parent-reported anthropometry and inform acceptable remote measurement practices among rural, preschool-aged children.

Methods: Parent-reported height, weight, body mass index (BMI), BMI z-score, and BMI percentile for their child were collected through surveys with the assessment of their source of home measure. Objective measures were collected by clinic staff at the child’s well-child visit (WCV). Agreement was assessed using correlations, alongside an exploration of the time gap (TG) between parent-report and WCV to moderate agreement. Using parent- and objectively reported BMI z-scores, weight classification agreement was evaluated. Correction equations were applied to parent-reported anthropometrics.

Results: A total of 55 subjects were included in this study. Significant differences were observed between parent- and objectively reported weight in the overall group (−0.24 kg; p = 0.05), as well as height (−1.8 cm; p = 0.01) and BMI (0.4 kg/m2; p = 0.02) in the ≤7d TG + Direct group. Parental reporting of child anthropometry ≤7d from their WCV with direct measurements yielded the strongest correlations [r = 0.99 (weight), r = 0.95 (height), r = 0.82 (BMI), r = 0.71 (BMIz), and r = 0.68 (BMI percentile)] and greatest classification agreement among all metrics [91.67% (weight), 54.17% (height), 83.33% (BMI), 91.67% (BMIz), and 33.33% (BMI percentile)]. Corrections did not remarkably improve correlations.

Discussion: Remote pediatric anthropometry is a valid supplement for clinical assessment, conditional on direct measurement within 7 days. In rural populations where socioenvironmental barriers exist to care and surveillance, we highlight the utility of telemedicine for providers and researchers.

1 Introduction

Childhood obesity poses an imminent threat to the wellbeing of children worldwide (1, 2). Obesity is associated with non-communicable diseases such as cardiovascular disease (CVD), type 2 diabetes mellitus (T2DM), musculoskeletal disorders, cancer, and increased mortality risk (2).

The coronavirus disease 2019 (COVID-19) pandemic has placed increased strain on children at risk or already classified as overweight or obese. The prevalence of childhood obesity has increased rapidly from 19.3 to 22.4% amid the pandemic (3). Children’s ability to achieve adequate physical activity has been hampered and supplanted with increased time spent engaged in sedentary behavior (4). The metabolic storm generated from the upheaval of physical activity exacerbates the progression of the disease state and worsens obesity-related sequelae (5).

A constellation of factors influences the presence of childhood obesity; however, the living environment and geography may predispose children to a greater likelihood of developing overweight or obesity. Specifically, children in rural areas face higher odds of developing obesity than those in urban areas (68). An array of socioenvironmental factors is associated with obesogenic disparities observed in rural children, some of which function as barriers to clinical care (8, 9). Rural patients face long clinic commutes, and those from low-income households may have unreliable transportation. The American Academy of Pediatrics (AAP) identifies telemedicine as an essential strategy to reduce such barriers (10). While utilization has increased during the pandemic, broadband technology access presents a novel barrier for rural patients (1113).

Telemedicine offers convenience but presents challenges for physical exams, as indicated in monitoring child growth. The use of age- and sex-specific body mass index (BMI) as an acceptable metric for classifying childhood overweight or obesity by providers was established by the US Preventative Services Task Force (USPSTF) in 2005 (14). The gold standard for anthropometric surveillance data is objectively measured height and weight, used to calculate BMI and related BMI indices (15). BMI indices are plotted on age- and sex-specific growth charts generated from population samples, establishing reference norms and allowing providers to determine where a child falls along the reference continuum (15). While variable for children in normal weight ranges due to variance in lean mass, BMI is associated with acceptable sensitivity as an indicator of adverse weight in children with an excess of adiposity (16).

Parent-proxy anthropometric reporting is an emerging strategy to supplement well-child visit (WCV) delays and demonstrate pediatric telemedicine utility. However, there are challenges in obtaining these metrics annually (15). WCV delays during the pandemic resulted in an aggravation of the existing concerns regarding annual anthropometric surveillance (17). To combat these concerns, a shift toward self- or parent-proxy-reported height and weight has been initiated to supplement clinical monitoring (15, 1828). Measurement continuity is crucial when seeking to collect valid proxy-report measures. Smart scales or other technologically advanced tools may be optimal, but socioeconomically disadvantaged populations (i.e., rural) rarely have sufficient access to technology allowing them to utilize these instruments (23). Studies using widely available measurement tools display utility, though they may be subject to the risk of reporting bias (23). Further, home measurements are more acceptable when solely using direct measurements (19). Bias mitigation strategies should include consideration of the time gap (TG) between parent-proxy reported and WCV anthropometrics (23, 2931). Parental underreporting of child weight and/or overreporting of child height are common in studies assessing the relationship between self-report and objective measures (18, 21, 22, 26). These inaccuracies are pronounced to a greater degree in children with pre-existing overweight or obesity (22, 32). Chronic misreporting can lead to chronic misrepresentation of BMI accuracy and the identification of overweight and obesity.

Correction equations for parent-reported height and weight have been assessed for their ability to ameliorate parental reporting bias (2931, 3339). These equations are derived from individual datasets, rendering them unique to sociodemographic characteristics from their reference sample (29, 35, 3739). As pediatric healthcare delivery in rural settings faces residual scheduling challenges and loss of follow-up amid a transition to telemedicine, validation of parent-reported height and weight in underrepresented age groups is pivotal (17, 40, 41). To date, there is limited evidence utilizing correction equations in preschool-aged children. Hence, the objectives of the present investigation are: (1) determining correlations between parent-reported and objective clinical measures (weight, height, BMI, BMI z-score, and BMI percentile); (2) assessing the impact of the TG between parent and clinical report on these relationships; (3) discerning whether the source of the home measure impacts the relationships (e.g., measured vs. estimated values); and (4) evaluating the utility of corrections and their ability to improve correlations between parent-reported and objective clinical measures.

2 Methods

2.1 Study context—secondary analysis using data from the ENCIRCLE study

The patient-cliNic-Community Integration to prevent obesity in Rural preschool ChiLdrEn (ENCIRCLE) study is a pragmatic, cluster randomized controlled trial (RCT) that was conducted across Geisinger primary care clinics in central and northeast Pennsylvania (42). This study was designed to compare the effectiveness of clinic, patient-clinic, or patient-clinic-community interventions to attenuate the prevalence of obesity among preschool-aged children exposed to obesogenic environments (42). Many of these clinic locations are rural and serve an array of socioeconomic backgrounds within their respective communities.

Primary care providers (PCPs) from family medicine (n = 51) or pediatric (n = 54) clinics were randomized to one of the three potential intervention arms: standard WCV, patient-reported outcome (PRO) enhanced WCV, or PRO enhanced WCV plus Food Care. The WCV arm consisted of routine care aligned with clinical practice guidelines, including BMI screening and provider-led counseling (43). The PRO WCV and PRO WCV plus Food Care arms both integrate the parent-reported Family Nutrition and Physical Activity (FNPA) risk assessment tool into the WCV (44, 45). Food Care enhancements to the intervention involved patient referrals to community health professionals responsible for providing evidence-based obesity prevention in conjunction with telehealth guidance on economical dietary planning (46). The ENCIRCLE study was incidentally launched in March 2020, in concordance with the COVID-19 pandemic. Telehealth has emerged as a critical component in maintaining continuous healthcare delivery amid efforts to mitigate transmission during the pandemic. The ENCIRCLE study was approved by Geisinger’s Institutional Review Board and is presently registered with ClinicalTrials.gov (NCT04406441).

2.2 Study participants

This study incorporates a subset of the ENCIRCLE study population that has both clinical and parent-reported height and weight metrics (n = 55) for children.

2.3 Data collection

2.3.1 Parent-proxy reported anthropometrics

Data collection from consenting parents included self-reported children’s age, biological sex, race/ethnicity, children’s height and weight, relationship to the child, educational level, annual household income indices, and employment status. Respondents indicated whether weight and height were estimated or measured directly at home. Values were reported to the nearest inch/cm and pound/kilogram. A screenshot of these questions is included (Supplementary Figure S1) as the parent would view them. No details about home equipment were collected.

2.3.2 Objectively assessed anthropometrics

Children’s height and weight were recorded using standardized procedures during WCVs by trained clinic staff. Height was measured to the nearest 0.1 cm using a stadiometer (SECA 264), and weight was measured to the nearest 0.1 kg using a calibrated digital scale (Health-o-meter 599KL).

2.3.3 Calculation of BMI, BMI z-score, and BMI percentile

Parent-proxy and objectively measured BMI were calculated from parent-reported and objectively measured height and weight, respectively. Children’s BMI z-score and BMI percentile for age and sex were calculated from the Centers for Disease Control (CDC) programs designed for children from 2 to 19 years of age.

2.3.4 Weight classifications

Sex-specific BMI-for-age percentiles were calculated in the EHR system to identify children by weight status: normal weight (> 5th and < 85th), overweight (≥ 85th and < 95th), obese (≥ 95th and < 99th), and severely obese (≥ 99th).

2.3.5 Population sociodemographic characteristics

Demographic characteristics of the ENCIRCLE study population were recorded into the REDCap database during the eligibility screening process and inclusion/exclusion survey criteria from consenting parents. Additional characteristics were collected during a study team follow-up call.

2.3.6 Correction methods

Correction equations were derived using an univariate analysis to determine subject characteristics to be applied to the correction model. Adjusted R2 statistics assess the fit of the model. The model in the present investigation was extrapolated from parents reporting their child’s height and weight ≤ 7 days prior to the WCV (n = 37) to accommodate the influence of the TG between parent-proxy and objective measurements. Indirect corrections for parent-proxy reported BMI, i.e., applying correction equations to parent-proxy reported height and weight to subsequently calculate a corrected BMI, were employed. Correction models were uniquely generated for our given dataset due to the lack of established correction models for preschool-aged children and consideration of previous literature that has advised against the application of correction equations to multiple datasets (34, 47, 48). Correction modeling procedures were carried out in SAS (SAS Institute, Cary, NC, USA).

2.4 Statistical analyses

To mitigate potential reporting bias in parent-proxy measurements, only anthropometrics that were reported prior to the child’s WCV were included in analyses. Sociodemographic factors were included to characterize the study population. Differences between parent-proxy and objective clinic measurements were reported to describe the distribution of height, weight, BMI, BMI z-score, and BMI percentile. The calculation of age- and sex-specific BMI z-scores and percentiles was performed using SAS procedures provided by the CDC. A stratification based on the TG was performed to identify differences between parent-proxy and objective anthropometrics. TG differences were applied to compare measurements that occurred ≤7 days before the WCV against measurements that occurred >7 days before the WCV. REDCap surveys were given to participating parents, representing each parent–child dyad. Parents were asked whether their reported measurements (height or weight) were directly measured or estimated. To differentiate subjects whose heights and weights were directly measured, TG groups (≤7 days and > 7 days) were subject to additional stratification based on survey responses.

Independent samples t-tests were employed to assess between-group differences for child demographic characteristics. Paired samples t-tests assess differences between parent-proxy and objectively reported measures (height, weight, BMI, BMI z-score, and BMI percentile). The significance level was set at a value of p of ≤0.05. Pearson’s correlation coefficient (R) acts as the ratio of covariance between variables and was calculated to assess the relationship between parent-proxy and objective measures. Scatter plots comparing parent-proxy and objective measures were generated to display correlations and the data distribution.

Bland–Altman plots were used to assess agreement between parent-proxy and objective measurements for height, weight, BMI, BMI z-score, and BMI percentile (47).

Sensitivity (true positive) and specificity (true negative) analyses were employed in the present analysis to discern weight classification error and agreement based on parent-proxy BMI z-score. In the present study, sensitivity identified the proportion of children who are objectively classified as obese and concurrently classified as obese by parent-proxy reports. Specificity identified the proportion of children who are objectively classified as non-obese and concurrently classified as non-obese by parent-proxy reports. Cutoff values for BMI z-score weight categories are described as normal (−2 SD > BMI > 1 SD), overweight (1 SD > BMI > 2 SD), and obese (BMI > 2 SD) in accordance with previous literature (48). Positive predictive value (PPV), negative predictive value (NPV), and accuracy were also calculated in the present analysis (48).

Cohen’s Kappa quantified the agreement of weight categorization (normal weight, overweight, or obese) between parent-proxy and objective measurements using calculated BMI z-scores. Cohen’s Kappa is interpreted by a range of scores from 0.0 to 1.0; <0 indicating a ‘less than chance’ agreement, 0.01–0.20 indicating a ‘slight’ agreement, 0.21–0.40 indicating ‘fair’ agreement, 0.41–0.60 indicating ‘moderate’ agreement, 0.61–0.80 indicating ‘substantial’ agreement, and 0.81–0.99 indicating ‘almost perfect’ agreement (49). The intraclass correlation coefficient (ICC) assessed the outcome variation between parent-proxy and objective measures (50). ICC is interpreted along a spectrum from 0.0 to 1.0, where values <0.5 are indicative of ‘poor reliability,’ values between 0.5 and 0.75 are indicative of ‘moderate’ reliability, values between 0.75 and 0.9 are indicative of ‘good’ reliability, and values >0.9 indicate ‘excellent’ reliability (51). Histograms were created, displaying the frequency of agreement between parent-proxy and objective measures.

3 Results

A total of 55 parent–child dyads represent the overall study population. Most children in this study were female (53%). The mean age at the time of parental reporting was 46.4 months, and 46.9 months at their WCV. The average TG between parent-report and WCV was 16.9 days. Demographic characteristics for all stratification groups are described in Table 1. Certain parental demographic data (i.e., parent gender, ethnicity, race, education, or employment) were calculated based on a smaller reference sample due to the presence of occasional missing survey report data.

Table 1
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Table 1. Demographic characteristics of the study population.

Regardless of the TG, parents tend to report their child’s height (74.5%) and weight (85.5%) as “1” (direct) most of the time. Parents reporting their child’s measurements >7 days before their WCV utilize direct measurements more for height (83.3%) and weight (94.4%) than those reporting ≤7 d (70.3, 81.1%, respectively).

Table 2 describes means, differences, and agreement analyses (ICC, Pearson’s R) for parent- and objectively reported anthropometrics for the overall study population, and individual stratification groups. A significant difference between parent-reported weight and objectively measured weight was detected across the overall sample (p = 0.05). Significant differences were detected for height (p = 0.01) and BMI (p = 0.02) in the ≤7d TG + Direct group.

Table 2
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Table 2. Means, differences, and agreement between parent-proxy reported measures and objective measures from clinic visits.

Weight classification agreement measured using Cohen’s Kappa for BMI z-score within the overall population yielded a Kappa coefficient of 0.22, indicating fair agreement.

Sensitivity, specificity, PPV, NPV, and accuracy are calculated using parent-proxy reported BMI z-score for weight classification, derived from parent-reported height and weight (Table 3). Sensitivity in normal weight subjects decreased as stratification level increased across the three groups (66, 60, 53%), and specificity increased similarly across the three groups (55, 83, 86%). Overweight specificity decreased across the three groups (67, 60, and 55%), and sensitivity increased (38, 71, and 100%). Sensitivity and specificity did not notably change among obese subjects.

Table 3
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Table 3. Sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of parent-reports for predicting weight classification with parent-reported BMI z-score.

Table 4 describes the classification accuracy of parent-reported anthropometrics for all stratification groups. Unanimously, the ≤7d TG + Direct group displayed the greatest level of classification agreement (weight, 91.67%; height, 54.17%; BMI, 83.33%; BMI z-score, 91.67%; and BMI percentile, 33.33%). Conversely, the >7d TG + Direct group displayed the lowest rates of classification agreement for height (26.67%) and weight (60%), while the >7d TG group displayed the lowest rates of classification agreement for all three BMI indices (BMI, 38.89%; BMI z-score, 55.56%; BMI percentile, 22.22%). An agreement gradient emerged across classification groups, ranking highest to lowest agreement from ≤7d TG + Direct, ≤7d TG, Overall, >7d TG + Direct, and > 7d TG.

Table 4
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Table 4. Accuracy of parent-proxy reported anthropometric data for weight, height, BMI, BMI z-score, and BMI percentile.

The limits of agreement (LOA) are representative of the mean difference ± 1.96 standard deviations and are calculated and displayed within each respective Bland–Altman plot (Supplementary Figures S2A–E). These include LOA for weight (1.48, −1.95), height (8.65, −10.31), BMI (3.2, −2.95), BMI z-score (2.19, −2.08), and BMI percentile (55.39, −57.87).

Correction models were applied to parent-reported height and weight, as subsequently described.

Corrected Weight = 0.489 + (0.984 * WeightSelf)

Corrected Height = 38.952 + (0.462 * HeightSelf) + (0.350 * months)

Correlations (Pearson’s R) were calculated to assess the agreement between corrected parent- and objectively reported height, weight, and indirectly calculated BMI. In the ≤7d TG + Direct group (n = 37), the weight correlation remained unchanged (0.99), decreased for height (0.95 to 0.94), and decreased for indirect BMI (0.82 to 0.72). In the >7d TG + Direct group (n = 15), weight correlation remained unchanged (0.93), height remained unchanged (0.89), and indirect BMI improved (0.53 to 0.63).

4 Discussion

Amid strong agreement between parent- and objectively reported height and weight within the overall population, BMI metrics (BMI, BMI z-score, and BMI percentile) were poorly correlated. Thus, we sought to explore stratification methods and corrections to strengthen this agreement. We observed the marked influence of the TG, noting that measurements recorded and reported within 7 days displayed higher indications of agreement when compared to those greater than 7 days from the child’s WCV. These improvements were augmented by controlling for the source of the home measure (i.e., including only direct measures). However, our application of corrections to parent-reported height, weight, and BMI did not accentuate agreement. Our findings support the utility of remote anthropometry under the conditions of reporting within 7 days and confirming that the child’s at-home measurement was direct.

Objective assessments performed by trained clinical staff are considered the gold standard of anthropometric assessment (15, 5255). As telemedicine becomes a staple of clinical practice in the wake of COVID-19, the validation of remote anthropometry in children has garnered increased attention (15, 1828). Previous research has leveraged pre-recorded at-home video instruction (23), live at-home video conference (37), and smart-scale technology (56, 57) when collecting height and weight remotely. In the present study, we neither provided home equipment nor collected specific information regarding tools that parents used to measure their children on their own accord. Regardless, we found that direct measurements indicated by survey responses positively impacted the agreement between parental and clinical raters. Skinner et al. underscore the importance of clarifying the source of the home measure, finding that younger children were more likely to be misclassified into an incorrect weight classification following parental guessing (19). Our findings are further supported by a recent investigation by Forseth et al. where negligible differences were found between the use of at-home, study-provided, or objectively measured (school-based stadiometer) height and weight among rural children (23). While measurement instructions may provide a feasible strategy to mitigate reporting bias, broadly accessible tools for home-based measurements are acceptable.

Our study is among the few to identify the TG between reported measures and objective assessments as a critical component of moderating agreement (29, 58). Cheng et al. provide a framework for examining the TG as it relates to reporting accuracy and stratifying their patient population into those reporting within 7 and 30 days, respectively. In line with our findings, this group found that reporting within 7 days of objective measurement was associated with a lesser difference between reported and objective assessments. We found that controlling for TGs within 7 days improved agreement for the overall sample. The magnitude of agreement was amplified when additional control for the source of the home measure was included. Our validation provides clinicians and researchers with an opportunity to enhance the accuracy of their use of remote anthropometry in telemedicine.

Accurate weight classification is critical for gauging the breadth of childhood overweight and obesity. The WHO recommends using BMI z-scores in research for the sake of continuity (59). Using a clinically measured BMI z-score as an anchor, we found parental reporting accuracy to gradually improve when controlling for the TG within 7 days, followed by a compounded increase in accuracy when controlling for the source of the home measure. Several reviews have identified a high prevalence of parental weight misclassification for their children (6064). A review by Sherry et al. found parental reporting of BMI to be 55–76% sensitive for identification, and the prevalence of overweight decreased by −0.4 to −17.7% when calculated BMI was derived from parental reports, indicating chronic underreporting (65). These findings align with ours, where overweight sensitivity was low for the overall parent-reported sample (38%), indicating poor ability to correctly classify children as overweight. Only when additional control was integrated for the TG within 7 days, a direct source of home measure, did sensitivity improve (38, 71, and 100%, respectively). While limited, the literature suggests that the rationale for parental reporting bias is potentially due to factors such as digit preference, inconsistent assessment timepoint, rounding error, and social desirability bias that may create misconceptions about their children’s weight (32, 6668). Further elucidation of socioenvironmental and interpersonal influences on parental weight misclassification is warranted.

Under- or overreporting of child height and weight typically yields poor agreement between BMI calculated from parental reporting and BMI calculated from objective measures (26, 29). Underestimations of BMI have been reported to the degree of 0.5 kg/m2 (26, 37) and 0.6 kg/m2, respectively (69). Shields et al. have identified BMI overreporting as well, by a margin of 0.7 kg/m2 based on parental reports (34). Our study finds BMI to be overestimated by 0.13 kg/m2, despite underreporting of height and weight within the overall sample. Correction modeling provides an opportunity to combat misreporting and improve agreement between parent- and objectively reported height, weight, and BMI (2931, 3339). In one study utilizing correction modeling, agreement quantified by ICC improved from 0.33 to 0.64 for the classification of overweight or obese status after indirect corrections were applied for reporting within 7 days (29). Ghosh-Dastidar et al. show increased sensitivity for obesity regardless of sex and smaller RMSE values using indirect corrections, while noting heterogeneity of model applicability due to gender and outcome (37). We sought to control out-of-context equation applications by generating our own equations for our population. We align our use of ‘indirect’ BMI corrections with research that has shown favorable outcomes using this modeling technique (29, 37). However, no improvements in agreement parameters were found in our study. We speculate that the heightened levels of agreement we were able to achieve when controlling for the TG and source of home measure negated the capacity for corrections to further improve these relationships.

We provide validation for the concordance between parent-reported and objectively measured data, although the present study is not without limitations. Our omission of collecting information about home equipment used to measure children’s height and weight stymies the evaluation of factors that may contribute to parental reporting bias. Additionally, our predominantly low-income, rural population may be inordinately impacted by a lack of internet access, hindering their capacity to engage with telehealth (70, 71). Additional limitations include the sample size and geographical constraints that restrict the generalizability of these findings to populations with comparable demographic characteristics. Overall, the present study serves to inform emergent literature regarding the use of parent-reported anthropometrics during the pandemic. These outcomes will advise clinicians, healthcare administrators, policymakers, and researchers who seek to leverage remote anthropometry as a supplement for clinical measures.

Data availability statement

The data analyzed in this study is subject to the following licenses/restrictions: the data from the present study are available from the corresponding author upon request. Requests to access these datasets should be directed to LB-D, ldbaileydavis@geisinger.edu.

Ethics statement

The studies involving humans were approved by the Declaration of Helsinki, and ethical approval was obtained from the Institutional Review Board of Geisinger (#2020–0207, Version 1.19, 9/7/2022). Informed consent and parental permission were obtained from all participants. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants’ legal guardians/next of kin.

Author contributions

BP: Formal analysis, Investigation, Methodology, Validation, Writing – original draft, Writing – review & editing. GW: Data curation, Formal analysis, Software, Supervision, Writing – review & editing. LB-D: Conceptualization, Funding acquisition, Methodology, Project administration, Resources, Supervision, Visualization, Writing – review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported through a Patient-Centered Outcomes Research Institute (PCORI®) Project Program Award (CER-2019C1-16040). All statements in this report, including its findings and conclusions, are solely those of the authors and do not necessarily represent the views of the PCORI, its Board of Governors, or the Methodology Committee.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnut.2024.1279931/full#supplementary-material

References

1. Centers for Disease Control and Prevention. Childhood obesity facts. (2022). Available at: https://www.cdc.gov/obesity/data/childhood.html

Google Scholar

2. World Health Organization. Obesity and overweight. (2021). Available at: https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight

Google Scholar

3. Lange, SJ, Kompaniyets, L, Freedman, DS, Kraus, EM, Porter, R, Blanck, HM, et al. Longitudinal trends in body mass index before and during the COVID-19 pandemic among persons aged 2–19 years — United States, 2018–2020. MMWR Morb Mortal Wkly Rep. (2021) 70:1278–83. doi: 10.15585/mmwr.mm7037a3

PubMed Abstract | Crossref Full Text | Google Scholar

4. Dunton, GF, Do, B, and Wang, SD. Early effects of the COVID-19 pandemic on physical activity and sedentary behavior in children living in the U.S. BMC Public Health. (2020) 20:1351. doi: 10.1186/s12889-020-09429-3

PubMed Abstract | Crossref Full Text | Google Scholar

5. Vogel, M, Geserick, M, Gausche, R, Beger, C, Poulain, T, Meigen, C, et al. Age- and weight group-specific weight gain patterns in children and adolescents during the 15 years before and during the COVID-19 pandemic. Int J Obes. (2021) 46:144–52. doi: 10.1038/s41366-021-00968-2

PubMed Abstract | Crossref Full Text | Google Scholar

6. Johnson, JA, and Johnson, AM. Urban-rural differences in childhood and adolescent obesity in the United States: a systematic review and meta-analysis. Child Obes. (2015) 11:233–41. doi: 10.1089/chi.2014.0085

PubMed Abstract | Crossref Full Text | Google Scholar

7. Davis, AM, Beaver, G, Dreyer Gillette, M, Nelson, E-L, Fleming, K, Swinburne Romine, R, et al. IAmHealthy: rationale, design and application of a family-based mHealth pediatric obesity intervention for rural children. Contemp Clin Trials. (2019) 78:20–6. doi: 10.1016/j.cct.2019.01.001

PubMed Abstract | Crossref Full Text | Google Scholar

8. Bailey-Davis, L, Horst, M, Hillemeier, MM, and Lauter, A. Obesity disparities among elementary-aged children: data from school-based BMI surveillance. Pediatrics. (2012) 130:1102–9. doi: 10.1542/peds.2012-0192

PubMed Abstract | Crossref Full Text | Google Scholar

9. Klitzman, P, Armstrong, B, and Janicke, DM. Distance as a predictor of treatment attendance in a family based pediatric weight management program in rural areas. J Rural Health. (2014) 31:19–26. doi: 10.1111/jrh.12078

PubMed Abstract | Crossref Full Text | Google Scholar

10. Committee on Pediatric WorkforceRimsza, ME, Hotaling, AJ, Keown, ME, Marcin, JP, Moskowitz, WB, et al. The use of telemedicine to address access and physician workforce shortages. Pediatrics. (2015) 136:202–9. doi: 10.1542/peds.2015-1253

PubMed Abstract | Crossref Full Text | Google Scholar

11. Ray, KN, Mehrotra, A, Yabes, JG, and Kahn, JM. Telemedicine and outpatient subspecialty visits among pediatric Medicaid beneficiaries. Acad Pediatr. (2020) 20:642–51. doi: 10.1016/j.acap.2020.03.014

PubMed Abstract | Crossref Full Text | Google Scholar

12. Jamison, S, Zheng, Y, Nguyen, L, Khan, FA, Tumin, D, and Simeonsson, K. Telemedicine and disparities in visit attendance at a rural pediatric primary care clinic during the COVID-19 pandemic. J Health Care Poor Underserved. (2023) 34:535–48. doi: 10.1353/hpu.2023.0048

PubMed Abstract | Crossref Full Text | Google Scholar

13. Schweiberger, K, Verma, R, Faulds, S, Jonassaint, CR, White, GE, and Ray, KN. Scheduled and attended pediatric primary care telemedicine appointments during COVID-19. Pediatr Res. (2023) 94:185–92. doi: 10.1038/s41390-023-02481-w

PubMed Abstract | Crossref Full Text | Google Scholar

14. Grossman, DC, Bibbins-Domingo, K, Curry, SJ, Barry, MJ, Davidson, KW, Doubeni, CA, et al. Screening for obesity in children and adolescents. JAMA. (2017) 317:2417. doi: 10.1001/jama.2017.6803

Crossref Full Text | Google Scholar

15. Akinbami, LJ, and Ogden, CL. Childhood overweight prevalence in the United States: the impact of parent-reported height and weight. Obesity. (2009) 17:1574–80. doi: 10.1038/oby.2009.1

PubMed Abstract | Crossref Full Text | Google Scholar

16. Freedman, DS, and Sherry, B. The validity of BMI as an indicator of body fatness and risk among children. Pediatrics. (2009) 124:S23–34. doi: 10.1542/peds.2008-3586e

Crossref Full Text | Google Scholar

17. Nguyen, KH, Nguyen, K, Lekshmi, D, Corlin, L, and Niska, RW. Delays in children’s preventive health services during the COVID-19 pandemic. Fam Med. (2022) 54:350–61. doi: 10.22454/fammed.2022.922801

Crossref Full Text | Google Scholar

18. Gordon, NP, and Mellor, RG. Accuracy of parent-reported information for estimating prevalence of overweight and obesity in a race-ethnically diverse pediatric clinic population aged 3 to 12. BMC Pediatr. (2015) 15:5. doi: 10.1186/s12887-015-0320-0

PubMed Abstract | Crossref Full Text | Google Scholar

19. Skinner, AC, Miles, D, Perrin, EM, Coyne-Beasley, T, and Ford, C. Source of parental reports of child height and weight during phone interviews and influence on obesity prevalence estimates among children aged 3–17 years. Public Health Rep. (2013) 128:46–53. doi: 10.1177/003335491312800107

PubMed Abstract | Crossref Full Text | Google Scholar

20. Dubois, L, and Girad, M. Accuracy of maternal reports of pre-schoolers’ weights and heights as estimates of BMI values. Int J Epidemiol. (2007) 36:132–8. doi: 10.1093/ije/dyl281

PubMed Abstract | Crossref Full Text | Google Scholar

21. Scholtens, S, Brunekreef, B, Visscher, TL, Smit, HA, Kerkhof, M, Jongste, JC, et al. Reported versus measured body weight and height of 4-year-old children and the prevalence of overweight. Eur J Public Health. (2007) 17:369–74. doi: 10.1093/eurpub/ckl253

PubMed Abstract | Crossref Full Text | Google Scholar

22. Tenenbaum, A, Shefer-Averbuch, N, Lazar, L, Yakobovitch-Gavan, M, Phillip, M, and Oron, T. Growth assessment of children during the COVID-19 pandemic—can we rely on parental measurements? Acta Paediatr. (2021) 110:3040–5. doi: 10.1111/apa.16034

PubMed Abstract | Crossref Full Text | Google Scholar

23. Forseth, B, Davis, AM, Bakula, DM, Murray, M, Dean, K, Swinburne Romine, RE, et al. Validation of remote height and weight assessment in a rural randomized clinical trial. BMC Med Res Methodol. (2022) 22:185. doi: 10.1186/s12874-022-01669-8

PubMed Abstract | Crossref Full Text | Google Scholar

24. Haddad, EN, Kojaoghlanian, T, and Comstock, SS. Moving toward remote, parent-reported measurements in pediatric anthropometrics for research and practice. Front Pediatrics. (2022) 10:838815. doi: 10.3389/fped.2022.838815

PubMed Abstract | Crossref Full Text | Google Scholar

25. Kee, CC, Lim, KH, Sumarni, MG, Teh, CH, Chan, YY, Nuur Hafizah, MI, et al. Validity of self-reported weight and height: a cross-sectional study among Malaysian adolescents. BMC Med Res Methodol. (2017) 17:85. doi: 10.1186/s12874-017-0362-0

PubMed Abstract | Crossref Full Text | Google Scholar

26. Chai, LK, Collins, CE, May, C, Holder, C, and Burrows, TL. Accuracy of parent-reported child height and weight and calculated body mass index compared with objectively measured anthropometrics: secondary analysis of a randomized controlled trial. J Med Internet Res. (2019) 21:e12532. doi: 10.2196/12532

PubMed Abstract | Crossref Full Text | Google Scholar

27. Shiely, F, Perry, IJ, Lutomski, J, Harrington, J, Kelleher, CC, McGee, H, et al. Temporal trends in misclassification patterns of measured and self-report based body mass index categories – findings from three population surveys in Ireland. BMC Public Health. (2010) 10:560. doi: 10.1186/1471-2458-10-560

PubMed Abstract | Crossref Full Text | Google Scholar

28. Gorber, SC, Tremblay, M, Moher, D, and Gorber, B. A comparison of direct vs. self-report measures for assessing height, weight and body mass index: a systematic review. Obes Rev. (2007) 8:307–26. doi: 10.1111/j.1467-789x.2007.00347.x

PubMed Abstract | Crossref Full Text | Google Scholar

29. Cheng, Y, Xu, H, Rissel, C, Phongsavan, P, Buchanan, L, Taki, S, et al. Estimation and feasibility of correction modelling for mother-reported child height and weight at 2 years using data from the Australian chat trial. Sci Rep. (2022) 12:21353. doi: 10.1038/s41598-022-25388-8

PubMed Abstract | Crossref Full Text | Google Scholar

30. Jansen, W, van de Looij-Jansen, PM, Ferreira, I, de Wilde, EJ, and Brug, J. Differences in measured and self-reported height and weight in Dutch adolescents. Ann Nutr Metab. (2006) 50:339–46. doi: 10.1159/000094297

PubMed Abstract | Crossref Full Text | Google Scholar

31. Shiely, F, Hayes, K, Perry, IJ, and Kelleher, CC. Height and weight bias: the influence of time. PLoS One. (2013) 8:e54386. doi: 10.1371/journal.pone.0054386

PubMed Abstract | Crossref Full Text | Google Scholar

32. Akerman, A, Williams, ME, and Meunier, J. Perception versus reality: an exploration of children’s measured body mass in relation to caregivers’ estimates. J Health Psychol. (2007) 12:871–82. doi: 10.1177/1359105307082449

Crossref Full Text | Google Scholar

33. Scholes, S, Ng Fat, L, Moody, A, and Mindell, JS. Does the use of prediction equations to correct self-reported height and weight improve obesity prevalence estimates? A pooled cross-sectional analysis of health survey for England data. BMJ Open. (2023) 13:e061809. doi: 10.1136/bmjopen-2022-061809

PubMed Abstract | Crossref Full Text | Google Scholar

34. Shields, M, Gorber, SC, Janssen, I, and Tremblay, MS. Obesity estimates for children based on parent-report versus direct measures. Can J Diabetes. (2011) 35:142–3. doi: 10.1016/s1499-2671(11)52024-6

Crossref Full Text | Google Scholar

35. Dutton, DJ, and McLaren, L. The usefulness of “corrected” body mass index vs. self-reported body mass index: comparing the population distributions, sensitivity, specificity, and predictive utility of three correction equations using Canadian population-based data. BMC Public Health. (2014) 14:430. doi: 10.1186/1471-2458-14-430

PubMed Abstract | Crossref Full Text | Google Scholar

36. Jain, RB . Regression models to predict corrected weight, height and obesity prevalence from self-reported data: data from BRFSS 1999–2007. Int J Obes. (2010) 34:1655–64. doi: 10.1038/ijo.2010.80

PubMed Abstract | Crossref Full Text | Google Scholar

37. Ghosh-Dastidar, M, Haas, AC, Nicosia, N, and Datar, A. Accuracy of BMI correction using multiple reports in children. BMC Obesity. (2016) 3:37. doi: 10.1186/s40608-016-0117-1

PubMed Abstract | Crossref Full Text | Google Scholar

38. Brettschneider, A-K, Schaffrath Rosario, A, Wiegand, S, Kollock, M, and Ellert, U. Development and validation of correction formulas for self-reported height and weight to estimate BMI in adolescents. Results from the Kiggs study. Obes Facts. (2015) 8:30–42. doi: 10.1159/000375109

PubMed Abstract | Crossref Full Text | Google Scholar

39. Rios-Leyvraz, M, Ortega, N, and Chiolero, A. Reliability of self-reported height and weight in children: a school-based cross-sectional study and a review. Nutrients. (2022) 15:75. doi: 10.3390/nu15010075

PubMed Abstract | Crossref Full Text | Google Scholar

40. Gonzalez, D, Karpman, M, Kenney, GM, and Zuckerman, S. Delayed and forgone health care for children during the COVID-19 pandemic. (2021). Available at: https://www.urban.org/sites/default/files/publication/103652/delayed-and-forgone-health-care-for-children-during-the-covid-19-pandemic_1.pdf

Google Scholar

41. Onimoe, G, Angappan, D, Chandar, MC, and Rikleen, S. Effect of COVID-19 pandemic on well child care and vaccination. Front Pediatrics. (2022) 10:873482. doi: 10.3389/fped.2022.873482

PubMed Abstract | Crossref Full Text | Google Scholar

42. Bailey-Davis, L, Moore, AM, Poulsen, MN, Dzewaltowski, DA, Cummings, S, DeCriscio, LR, et al. Comparing enhancements to well-child visits in the prevention of obesity: encircle cluster-randomized controlled trial. BMC Public Health. (2022) 22:2429. doi: 10.1186/s12889-022-14827-w

PubMed Abstract | Crossref Full Text | Google Scholar

43. Daniels, SR, Hassink, SG, Abrams, SA, Corkins, MR, de Ferranti, SD, Golden, NH, et al. The role of the pediatrician in primary prevention of obesity. Pediatrics. (2015) 136:e275–92. doi: 10.1542/peds.2015-1558

PubMed Abstract | Crossref Full Text | Google Scholar

44. Ihmels, MA, Welk, GJ, Eisenmann, JC, Nusser, SM, and Myers, EF. Prediction of BMI change in young children with the family nutrition and physical activity (FNPA) screening tool. Ann Behav Med. (2009) 38:60–8. doi: 10.1007/s12160-009-9126-3

PubMed Abstract | Crossref Full Text | Google Scholar

45. Peyer, KL, Bailey-Davis, L, and Welk, G. Development, applications, and refinement of the family nutrition and physical activity (FNPA) child obesity prevention screening. Health Promot Pract. (2020) 22:456–61. doi: 10.1177/1524839920922486

PubMed Abstract | Crossref Full Text | Google Scholar

46. Pooler, JA, Morgan, RE, Wong, K, Wilkin, MK, and Blitstein, JL. Cooking matters for adults improves food resource management skills and self-confidence among low-income participants. J Nutr Educ Behav. (2017) 49:545–553.e1. doi: 10.1016/j.jneb.2017.04.008

PubMed Abstract | Crossref Full Text | Google Scholar

47. Gorber, SC, and Tremblay, MS. The bias in self-reported obesity from 1976 to 2005: a Canada–US comparison. Obesity. (2010) 18:354–61. doi: 10.1038/oby.2009.206

PubMed Abstract | Crossref Full Text | Google Scholar

48. Visscher, TL, Viet, AL, Kroesbergen, HT, and Seidell, JC. Underreporting of BMI in adults and its effect on obesity prevalence estimations in the period 1998 to 2001. Obesity. (2006) 14:2054–63. doi: 10.1038/oby.2006.240

PubMed Abstract | Crossref Full Text | Google Scholar

49. Anderson, LN, Carsley, S, Lebovic, G, Borkhoff, CM, Maguire, JL, Parkin, PC, et al. Misclassification of child body mass index from cut-points defined by rounded percentiles instead of Z-scores. BMC Res Notes. (2017) 10:639. doi: 10.1186/s13104-017-2983-0

Crossref Full Text | Google Scholar

50. Giavarina, D . Understanding bland altman analysis. Biochem Med. (2015) 25:141–51. doi: 10.11613/bm.2015.015

PubMed Abstract | Crossref Full Text | Google Scholar

51. Monaghan, TF, Rahman, SN, Agudelo, CW, Wein, AJ, Lazar, JM, Everaert, K, et al. Foundational statistical principles in medical research: sensitivity, specificity, positive predictive value, and negative predictive value. Medicina. (2021) 57:503. doi: 10.3390/medicina57050503

PubMed Abstract | Crossref Full Text | Google Scholar

52. Viera, AJ, and Garrett, JM. Understanding interobserver agreement: the kappa statistic U.S. Fam. med. (2005).

Google Scholar

53. Watson, PF, and Petrie, A. Method agreement analysis: a review of correct methodology. Theriogenology. (2010) 73:1167–79. doi: 10.1016/j.theriogenology.2010.01.003

Crossref Full Text | Google Scholar

54. Koo, TK, and Li, MY. A guideline of selecting and reporting intraclass correlation coefficients for reliability research. J Chiropr Med. (2016) 15:155–63. doi: 10.1016/j.jcm.2016.02.012

PubMed Abstract | Crossref Full Text | Google Scholar

55. Hodge, JM, Shah, R, McCullough, ML, Gapstur, SM, and Patel, AV. Validation of self-reported height and weight in a large, nationwide cohort of U.S. adults. PLoS One. (2020) 15:e0231229. doi: 10.1371/journal.pone.0231229

PubMed Abstract | Crossref Full Text | Google Scholar

56. Villanueva, EV . The validity of self-reported weight in US adults: a population based cross-sectional study. BMC Public Health. (2001) 1:11. doi: 10.1186/1471-2458-1-11

PubMed Abstract | Crossref Full Text | Google Scholar

57. Voss, LD, and Bailey, BJ. Equipping the community to measure children’s height: the reliability of portable instruments. Arch Dis Child. (1994) 70:469–71. doi: 10.1136/adc.70.6.469

PubMed Abstract | Crossref Full Text | Google Scholar

58. Bowring, AL, Peeters, A, Freak-Poli, R, Lim, MS, Gouillou, M, and Hellard, M. Measuring the accuracy of self-reported height and weight in a community-based sample of young people. BMC Med Res Methodol. (2012) 12:175. doi: 10.1186/1471-2288-12-175

PubMed Abstract | Crossref Full Text | Google Scholar

59. Pebley, K, Klesges, RC, Talcott, GW, Kocak, M, and Krukowski, RA. Measurement equivalence of e-scale and in-person clinic weights. Obesity. (2019) 27:1107–14. doi: 10.1002/oby.22512

PubMed Abstract | Crossref Full Text | Google Scholar

60. Ross, KM, and Wing, RR. Concordance of in-home ‘smart’ scale measurement with body weight measured in-person. Obes Sci Pract. (2016) 2:224–48. doi: 10.1002/osp4.41

PubMed Abstract | Crossref Full Text | Google Scholar

61. Brettschneider, A-K, Schienkiewitz, A, Schmidt, S, Ellert, U, and Kurth, B-M. Updated prevalence rates of overweight and obesity in 4- to 10-year-old children in Germany. Results from the telephone-based Kiggs wave 1 after correction for bias in parental reports. Eur J Pediatr. (2017) 176:547–51. doi: 10.1007/s00431-017-2861-8

PubMed Abstract | Crossref Full Text | Google Scholar

62. Wang, Y, and Chen, H-J. Use of percentiles and Z-scores in anthropometry In: V Preedy , editor. Handbook of anthropometry. New York, NY: Springer (2012)

Google Scholar

63. Tompkins, CL, Seablom, M, and Brock, DW. Parental perception of child’s body weight: a systematic review. J Child Fam Stud. (2014) 24:1384–91. doi: 10.1007/s10826-014-9945-0

Crossref Full Text | Google Scholar

64. Rietmeijer-Mentink, M, Paulis, WD, van Middelkoop, M, Bindels, PJE, and van der Wouden, JC. Difference between parental perception and actual weight status of children: a systematic review. Matern Child Nutr. (2012) 9:3–22. doi: 10.1111/j.1740-8709.2012.00462.x

PubMed Abstract | Crossref Full Text | Google Scholar

65. Doolen, J, Alpert, PT, and Miller, SK. Parental disconnect between perceived and actual weight status of children: a metasynthesis of the current research. J Am Acad Nurse Pract. (2009) 21:160–6. doi: 10.1111/j.1745-7599.2008.00382.x

PubMed Abstract | Crossref Full Text | Google Scholar

66. Towns, N, and D’Auria, J. Parental perceptions of their child’s overweight: an integrative review of the literature. J Pediatr Nurs. (2009) 24:115–30. doi: 10.1016/j.pedn.2008.02.032

PubMed Abstract | Crossref Full Text | Google Scholar

67. Parry, LL, Netuveli, G, Parry, J, and Saxena, S. A systematic review of parental perception of overweight status in children. J Ambulatory Care Manag. (2008) 31:253–68. doi: 10.1097/01.jac.0000324671.29272.04

PubMed Abstract | Crossref Full Text | Google Scholar

68. Phipps, S, Burton, P, Lethbridge, L, and Osberg, L. Measuring obesity in young children. Can Public Policy. (2004) 30:349. doi: 10.2307/3552519

Crossref Full Text | Google Scholar

69. Van Cauwenberghe, J, Delvaux, I, Michels, N, Den Hond, E, Schoeters, G, Nelen, V, et al. Validity of parentally reported versus measured weight, length and waist in 7- to 9-year-old children for use in follow-up studies. Eur J Pediatr. (2014) 173:921–8. doi: 10.1007/s00431-014-2274-x

PubMed Abstract | Crossref Full Text | Google Scholar

70. Ramsetty, A, and Adams, C. Impact of the digital divide in the age of covid-19. J Am Med Inform Assoc. (2020) 27:1147–8. doi: 10.1093/jamia/ocaa078

PubMed Abstract | Crossref Full Text | Google Scholar

71. Sherry, B . Accuracy of adolescent self-report of height and weight in assessing overweight status: a literature review. Arch Pediatr Adolesc Med. (2007) 161:1154–61. doi: 10.1001/archpedi.161.12.1154

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: remote anthropometry, parent-report anthropometry, child weight classification, child growth monitoring, pediatric telemedicine, BMI corrections, obesity detection, healthcare during COVID-19

Citation: Potts BA, Wood GC and Bailey-Davis L (2024) Agreement between parent-report and EMR height, weight, and BMI among rural children. Front. Nutr. 11:1279931. doi: 10.3389/fnut.2024.1279931

Received: 18 August 2023; Accepted: 13 February 2024;
Published: 01 March 2024.

Edited by:

Jared M. Tucker, Helen DeVos Children’s Hospital, United States

Reviewed by:

Sarah Comstock, Michigan State University, United States
Theresa V. Strong, Foundation for Prader-Willi Research, United States

Copyright © 2024 Potts, Wood and Bailey-Davis. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lisa Bailey-Davis, ldbaileydavis@geisinger.edu

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