Self-Reported Physical Activity and Exercise Patterns in Children With Sickle Cell Disease

2017 ◽  
Vol 29 (3) ◽  
pp. 388-395 ◽  
Author(s):  
Osarhiemen A. Omwanghe ◽  
Devin S. Muntz ◽  
Soyang Kwon ◽  
Simone Montgomery ◽  
Opeyemi Kemiki ◽  
...  

Purpose:Sickle cell disease (SCD) significantly affects physical functioning. We examined physical activity (PA) patterns in children with SCD versus a national sample and factors associated with PA and participation in physical education and organized sports.Method:One hundred children with SCD completed a 58-item survey with questions from the 2009–2010 National Health and Nutrition Examination Survey (NHANES) Physical Activity Questionnaire and others on physical education and sports, disease impact, and physical functioning.Results:Compared with NHANES participants, more children with SCD (67 vs 42%, p < .01) reported doing at least 10 min of moderate-to-vigorous intensity PA (MVPA)/week. Children with SCD also reported spending more days in MVPA (2.3 vs. 1.4 days/week, p < .01). However, fewer reported spending ³ 60 min/day in either vigorous PA (VPA) (24 vs. 43%, p = .01) or MVPA (17 vs 23%, p < .01). In addition, 90% and 48% of children with SCD participated in physical education and sports, respectively. Greater disease impact on PA and physical functioning were associated with lower participation.Conclusion:Children with SCD are active at moderate to vigorous intensity for shorter durations. Negative personal beliefs about disease impact and poor physical functioning represent barriers to PA in SCD.

Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 4099-4099 ◽  
Author(s):  
Osarhiemen A. Omwanghe ◽  
Soyang Kwon ◽  
Devin S. Muntz ◽  
Simone Montgomery ◽  
Opeyemi Kemiki ◽  
...  

Abstract Background Sickle cell disease (SCD) and its complications have a major impact on physical functioning in affected children and adolescents. However, little is known about habitual physical activity patterns and exercise routines in this population. The aims of this study were to evaluate the amount of time spent in moderate (MPA) or vigorous (VPA) physical activity, examine participation in school-based physical education or organized sports, and explore factors that influence physical activity or exercise habits in children and adolescents with SCD. Methods A58-question, self-administered survey was given to a cross-sectional group of children with SCD (all genotypes) in grades 6 through 12 followed in the Comprehensive Sickle Cell Programs at Ann & Robert H. Lurie Children’s Hospital of Chicago and the University of Illinois at Chicago. Children on hydroxyurea therapy and chronic transfusions were included. The survey included 2 sections: 1) questions adapted from the National Health and Nutrition Examination Survey (NHANES) Physical Activity Questionnaire and 2) supplemental questions addressing participation in school-based physical education and organized sports; disease severity and impact on physical activity; and attitudes about physical activity and exercise. We performed standard descriptive analyses and bivariate analysis using Pearson’s chi-square or Student’s t-test for independent samples for comparison of categorical and continuous data, respectively. Responses from NHANES questions were compared to age, sex and race matched data collected from the 2009-2010 NHANES survey. Results A total of 88 surveys have been collected to date. Among respondents with SCD, 59% were between 11 and 15 years old, 51% were male, 66% had hemoglobin SS disease, 44% were on hydroxyurea and 19% were on chronic transfusions. Data were compared to extracted data from 1362 NHANES participants weighted to adjust for differences in distributions in age, sex and race between groups. The proportion of children with SCD who reported at least 10 minutes of VPA in a typical week (66 vs. 65%, p = 0.91) and their frequency of VPA (2.8 vs. 2.5 days per week, p = 0.44) did not differ from that of children from the NHANES cohort. However, a higher proportion of children with SCD reported MPA (67 vs. 42%, p < 0.001) with a frequency (2.3 vs. 1.4 days per week, p < 0.001) that was significantly higher than that reported in NHANES. The duration of VPA or MPA on a typical day also differed significantly between groups. Compared to children from NHANES, fewer children with SCD reported spending more than 60 minutes in VPA or MPA on a typical day. Overall, only 13% of children with SCD met US physical activity guidelines recommending at least 60 minutes of physical activity every day. Of those children with SCD surveyed, 47% reported participating in school-based sports teams or physical activity clubs and 74% reported participating in physical education when offered at their school. Finally, we examined those variables that were associated with physical activity and participation in organized sports or physical education in children with SCD. Children 11 to 15 years old, when compared to children greater than 15 years old, were more likely to report 60 min of physical activity on more than 2 days per week (73 vs. 27%, p < 0.05). However, neither age nor sex affected participation in organized sports or physical education. We found that physical activity and participation in organized sports or physical education were not significantly affected by respondent beliefs regarding the impact of SCD on enjoyment of those activities. Sickle cell genotype, hydroxyurea use, chronic transfusions, and parental and personal attitudes toward physical activity also had no influence on participation in physical activity, organized sports or physical education in children with SCD. Conclusions When compared to matched peers in the NHANES study, children with SCD participate in comparable levels of VPA and even exceed their peers in levels of MPA. Participation in school-based organized sports and physical education was also common in children with SCD despite the previously reported impact of SCD on physical functioning in this population. Further studies are needed to determine the safety and potential health benefits of regular exercise and athletic participation in this population. Disclosures No relevant conflicts of interest to declare.


Author(s):  
Mohsen Saleh Elalfy ◽  
Ahmed Samir Ibrahim ◽  
Ghada Samir Ibrahim ◽  
Hanaa Midhat Abdel Gader Hussein ◽  
Hend Galal Eldeen Mohammed ◽  
...  

Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 3405-3405 ◽  
Author(s):  
Shawn M Bediako ◽  
Julie Nelson ◽  
Cody Cichowitz ◽  
Tiffany Yu ◽  
C. Patrick Carroll ◽  
...  

Abstract Background: The life span of individuals living with sickle cell disease (SCD) has increased considerably over the past three decades. Yet, as this group ages, new concerns emerge about their overall health profile - particularly with regard to cardiovascular disease (CVD), the primary cause of mortality in the United States. Metabolic syndrome (MetS) is a cluster of conditions that are associated with a 2-fold increase in CVD outcomes and a 1.5-fold increase in all-cause mortality. Little is known, however, about the prevalence of MetS risk factors among adults with SCD. As part of exploring the CVD profile of this population, we report findings from a pilot study that sought to evaluate MetS (typically defined as the presence of 3 or more risk factors). Methods: 49 adults (ages 21-66 years; 72% female) completed demographic and health behavior surveys, health-related family and personal histories, anthropometric measurements, the Block 2005 nutritional assessment, and a comprehensive blood panel. In terms of SCD genotype, 63% of participants were diagnosed with homozygous sickle cell anemia and 37% were diagnosed with hemoglobin SC disease. Descriptive and inferential statistics were used to summarize and compare MetS components stratified in separate analyses by genotype and sex. Results: The most prevalent MetS risk factors observed in our study - large waist circumference and reduced HDL levels - affected 45% and 69% of the sample, respectively. Overall, 16% of participants met traditional criteria for MetS. Table 1 summarizes mean values and shows the gender-adjusted risk for MetS. Although 78% of the sample self-reported moderate to high physical activity, nearly half of participants were overweight and had dietary saturated fat intake levels that exceeded both the national average and US Dietary Guidelines (<10%). Participants with the SC phenotype were older, consumed more calories, and had higher BMI, waist circumference, and BP values compared to those with the SS phenotype. Overall, males had worse MetS risk profiles compared to women, but no statistically significant sex differences were observed with regard to components of MetS. Conclusion: We report prevalence of MetS components, a surrogate of CVD risk, in a sample of adults living with SCD. Despite high levels of self-reported physical activity, both increased waist circumference and reduced HDL levels were notably high in our sample. These findings correspond with recent studies that indicate an upward trend in obesity and BMI among young adults with SCD. They also suggest a need to prioritize weight management, aerobic exercise, and resistance training strategies that could decrease MetS risk, but are rarely considered for this population. Table 1. Metabolic syndrome risk among adults living with SCD (N=49) Mean Value (SD) Proportion at Risk* Male (n = 14) Female (n = 35) Male (n = 14) Female (n = 35) Age (years) 41.6 (10.76) 39.3 (12.86) - - Waist circumference (cm) 96.53 (21.99) 90.75 (14.05) 42.9% 45.7% Triglycerides (mg/dL) 114.21 (57.22) 83.36 (36.21) 21.4% 3.0% HDL (mg/dL) 35.07 (9.51) 51.30 (20.31) 78.6% 69.7% Systolic BP 115.79 (15.00) 108.59 (13.15) 21.4% 8.6% Diastolic BP 69.11 (8.99) 62.17 (6.18) 0.0% 0.0% Fasting Glucose (mg/dL) 86.50 (8.07) 80.91 (13.73) 0.0% 9.0% Metabolic Syndrome - - 28.6% 8.6% *"Risk" is defined as: waist circumference > 89cm (Females) and > 102cm (Males); triglyceride levels > 150mg/dL; HDL levels < 50mg/dL (Females) and < 40mg/dL (Males); systolic blood pressure > 130; diastolic blood pressure > 85; fasting glucose levels > 100mg/dL. Disclosures No relevant conflicts of interest to declare.


2016 ◽  
pp. jsw061 ◽  
Author(s):  
Cynthia W. Karlson ◽  
Anna M. Baker ◽  
Maggie H. Bromberg ◽  
Thomas David Elkin ◽  
Suvankar Majumdar ◽  
...  

2020 ◽  
Vol 9 (9) ◽  
pp. e998998120
Author(s):  
Gabriella Aguiar Rodrigues Veras ◽  
Caroline Maria Igrejas Lopes ◽  
Ana Cláudia Alves e Luna ◽  
Valdenice Aparecida de Menezes

To assess the health-related quality of life of children and adolescents with sickle cell disease (SCD). This is a cross-sectional study carried out with 97 male and female patients aged 5 to 18 years with clinical and laboratory diagnosis of SCD, seen at the Hematology and Hemotherapy Hospital of Pernambuco. The Pediatric Quality of Life InventoryTM questionnaires, version 4.0 – child/adolescent report – were applied. Most patients were female (76.3%), had sickle cell anemia (89.7%) and mixed race (59.8%). There was a significant association in the psychosocial domain between age groups 5 to 7 (72.10) and 8 to 12 years (p≤0.05), the latter of which had the worst quality of life score (65.36). There were significant differences between sexes only in patients aged 13 to 18 years for physical functioning and for the overall mean of the domains. The means in both cases were higher in female patients than in male ones (70.89 x 56.88 for physical functioning and 71.72 x 59.77 for the overall mean of the domains). Poor quality of life was observed among children and adolescents with SCD, with negative impacts according to age and sex.


2004 ◽  
Vol 33 (8) ◽  
pp. 799-803 ◽  
Author(s):  
C Brachet ◽  
N Azzi ◽  
A Demulder ◽  
C Devalck ◽  
A Gourdin ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document