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1

Cochrane, E., S. Young, and Z. Shariff. "Acute compartment syndrome in a patient with sickle cell disease." Annals of The Royal College of Surgeons of England 102, no. 9 (2020): e1-e2. http://dx.doi.org/10.1308/rcsann.2020.0160.

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Haemoglobin SC (HbSC) disease accounts for 30% of cases of sickle cell disease in the United Kingdom and the United States. Unlike other sickle cell carriers, who are relatively asymptomatic, people with HbSC disease have a combination of genotypes with the potential to cause considerable morbidity due to intracellular water loss. Patients can present with acute pain, acute chest syndrome, proliferative retinopathy, splenic and renal complications, or stroke. We present a young man with HbSC disease who developed acute compartment syndrome. This is only the second report of this syndrome in a
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2

Tanaka, Chiaki, Akira Kyan, Minoru Takakura, Tim Olds, Natasha Schranz, and Shigeho Tanaka. "Validation of the Physical Activity Questions in the World Health Organization Health Behavior in School-Aged Children Survey Using Accelerometer Data in Japanese Children and Adolescents." Journal of Physical Activity and Health 18, no. 2 (2021): 151–56. http://dx.doi.org/10.1123/jpah.2019-0671.

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Background: An international physical activity (PA) questionnaire is beneficial to make cross-country comparisons among children and adolescents. This study assesses the validity of the PA questions in the World Health Organization Health Behavior in School-Aged Children (WHO HBSC) survey in Japanese children and adolescents. Methods: Participants were fifth- to sixth-grade Japanese primary school students (67 students aged 10.8 [0.5] y) and first- to third-grade junior high school students (108 students aged 13.0 [0.7] y). The Japanese version of the PA questions in the WHO HBSC (WHO HBSC-J)
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3

Vieira, Camilo, Isa Lyra, and Marilda Goncalves. "Evaluation of Transcranial Doppler in 1135 Sickle Cell Disease Children From Brazil: What Is the Time Averaged Maximum Velocity for High Risk of Stroke Among HbSC Patients?" Blood 120, no. 21 (2012): 1003. http://dx.doi.org/10.1182/blood.v120.21.1003.1003.

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Abstract Abstract 1003 Introduction. Sickle cell disease (SCD) is an autosomal recessive hereditary disorder, characterized by the presence of hemoglobin S (HbS), and a clinical multisystem involvement. Stroke is the most disabling complication of SCD and has an incidence around 11% and 2% in sickle cell anemia (HbSS) and SCD patients before the age of 20 respectively. The Transcranial Doppler (TCD) is a noninvasive and safe diagnostic technique to monitor the cerebral mean blood flow velocities of SCD identifying those at risk for developing stroke, enabling the prophylactic treatment with ch
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4

Sathi, Bindu K., Yoshida Yilin, Michael Raymond Weaver, et al. "Unusually High Prevalence of Silent Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease." Blood 134, Supplement_1 (2019): 2276. http://dx.doi.org/10.1182/blood-2019-122975.

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Introduction Children and adults with sickle cell disease (SCD) suffer from overt stroke, the prevalence of which has been reported to be 11% < 20 years. More commonly, they suffer from silent cerebral Infarction (SCI) that has a reported prevalence of 37.1% in children at 4 years of age1. Unlike homozygous SS disease (HbSS), the reported prevalence of overt and silent stroke in Hemoglobin SC (HbSC) is low (0% and 5.8%, respectively) in Cooperative Study of Sickle Cell Disease (CSSD)2. However, in a recent study, the prevalence of silent stroke in HbSC was found to be 13.5%3. The goal of ou
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5

Koller, Theadora, Antony Morgan, Ana Guerreiro, Candace Currie, and Erio Ziglio. "Addressing the socioeconomic determinants of adolescent health: experiences from the WHO/HBSC Forum 2007." International Journal of Public Health 54, S2 (2009): 278–84. http://dx.doi.org/10.1007/s00038-009-5420-x.

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6

Németh, Ágnes. "Új adatok a magyar serdülőkorúak egészséget befolyásoló szokásairól és egészségi állapotáról." Egészségfejlesztés 61, no. 1 (2020): 84–85. http://dx.doi.org/10.24365/ef.v61i1.561.

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Megjelent az Iskoláskorú gyermekek egészségmagatartása (Health Behaviour in School-aged Children, HBSC) elnevezésű, az Egészségügyi Világszervezettel (WHO) együttműködésben megvalósuló nemzetközi kutatás legújabb hazai vizsgálatának kutatási jelentése. A Kamaszéletmód Magyarországon című kötet a L’Harmattan Kiadó gondozásában jelent meg; a felmérést és a tanulmányt az ELTE PPK Pszichológiai Intézetének HBSC Kutatócsoportja készítette. A standard nemzetközi módszertan szerint folyó kutatásban négyévenként kerül sor felmérésre a 11-17 éves diákok országosan reprezentatív mintáján, név nélküli ké
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7

Santos, Teresa, Margarida Gaspar de Matos, Maria Celeste Simões, Helena Fonseca, and Maria do Céu Machado. "Individual factors related to chronic condition in Portuguese adolescents: Highlights from the HBSC/WHO study." Health 05, no. 11 (2013): 25–34. http://dx.doi.org/10.4236/health.2013.511a2005.

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8

Carvalho, Flávia, Ariani Souza, Ana Ferreira, et al. "Profile of Reproductive Issues Associated with Different Sickle Cell Disease Genotypes." Revista Brasileira de Ginecologia e Obstetrícia / RBGO Gynecology and Obstetrics 39, no. 08 (2017): 397–402. http://dx.doi.org/10.1055/s-0037-1604179.

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Purpose To describe the reproductive variables associated with different sickle cell disease (SCD) genotypes and the influence of contraceptive methods on acute painful episodes among the women with the homozygous hemoglobin S (HbSS) genotype. Methods A cross-sectional study was conducted between September of 2015 and April of 2016 on 158 women afflicted with SCD admitted to a hematology center in the Northeast of Brazil. The reproduction-associated variables of different SCD genotypes were assessed using the analysis of variance (ANOVA) test to compare means, and the Kruskal-Wallis test to co
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9

Charrier, Lorena, Paola Berchialla, Daniela Galeone, et al. "Smoking Habits among Italian Adolescents: What Has Changed in the Last Decade?" BioMed Research International 2014 (2014): 1–8. http://dx.doi.org/10.1155/2014/287139.

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Tobacco use, alcohol abuse, overweight and obesity are risk factors for numerous diseases in Italy as elsewhere. However, children and adolescents are not usually included in official national surveys although it is at this stage of life when unhealthy habits are often established. Italian participation in HBSC and GYTS surveys allows our country to implement standardized surveillance systems providing reliable information on tobacco-related behaviors of this population. Data from three HBSC surveys (2002–2010) show that following the drop in the first half of the decade, prevalence of tobacco
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10

Vereecken, Carine A., and Lea Maes. "A Belgian study on the reliability and relative validity of the Health Behaviour in School-Aged Children food-frequency questionnaire." Public Health Nutrition 6, no. 6 (2003): 581–88. http://dx.doi.org/10.1079/phn2003466.

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AbstractObjective:In the Health Behaviour in School-Aged Children (HBSC) survey, the frequency of consumption of a limited number of food items – focusing on fibre, calcium and less healthy items – is queried using a 15-item food-frequency questionnaire (FFQ). The present study was conducted to assess the reliability and relative validity of the HBSC FFQ among school pupils in Belgium.Design and subjects:To assess the reliability of the FFQ, 207 pupils aged 11–12 years and 560 pupils aged 13–14 years completed the questionnaire twice, with a test–retest interval of 6 to 15 days. To assess the
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11

Bondar, T. V. "Factors of the influence on self-determination of the life-style of teenagers." Ukrainian society 26, no. 3 (2008): 7–16. http://dx.doi.org/10.15407/socium2008.03.007.

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On the basis of data of a study executed in Ukraine in the frame of the international project of WHO “Health Behaviour Schoolage Children” (“HBSC”), the influence of such factors as socio-economic inequality, completeness of a family, mutual understanding with parents, attitude to school, and relations with teachers and children of the same age on the lifestyle of teenagers is analyzed.
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12

Isa, Tsunenori, Ryuichi Sawa, Kohtaroh Torizawa, et al. "Reliability and Validity of the Japanese Version of the Physical Activity Questionnaire for Older Children." Clinical Medicine Insights: Pediatrics 13 (January 2019): 117955651983583. http://dx.doi.org/10.1177/1179556519835833.

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Objectives: This study aimed to examine the reliability and validity of the Japanese version of the Physical Activity Questionnaire for Older Children (PAQ-C) in Japanese children aged 9 to 12 years. Methods: A total of 210 children aged between 9 and 12 years participated. Internal consistency and test-retest reliability were evaluated using Cronbach alpha coefficient and intraclass correlation coefficient (ICC), respectively. Validity was evaluated using athletic competence (AC), self-efficacy (SE), body mass index (BMI), body fat percentage (%BF), cardiovascular fitness (CVF), and World Hea
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13

Kesse-Adu, Rachel, Ronwyn Cartwright, Nicky Thomas, Eugene Oteng-ntim, and Jo Howard. "Feritility and Attitudes To Fertility In a Cohort Of Women With Sickle Cell disease In South East London." Blood 122, no. 21 (2013): 4686. http://dx.doi.org/10.1182/blood.v122.21.4686.4686.

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Introduction Women with Sickle Cell Disease (SCD) have been reported to have delayed menarche, increased rates of miscarriage & still birth. There is little evidence of the impact of SCD severity on fertility, or of patients’ attitudes towards their fertility. Methods Following IRB approval, an anonymised questionnaire was distributed to female patients over the age of 16 attending an SCD clinic. This included questions on menarche, fertility, reproductive history & clinical severity. We also surveyed attitudes to fertility & the role of fertility treatment. Results 101 women gave
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14

Zaborskis, Apolinaras, Nida Žemaitienė, Linas Šumskas, Vilius Grabauskas, Aurelijus Veryga, and Robertas Petkevičius. "Trends in alcohol consumption among Lithuanian school-aged children in 1994–2006 and new challenges." Medicina 44, no. 8 (2008): 623. http://dx.doi.org/10.3390/medicina44080081.

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Alcohol abuse is considered one of the most important risk-taking behaviors among young people in the world. This paper presents the results of the WHO collaborative cross-national study on Health Behavior in School-aged Children (HBSC) carried out in Lithuania and other European countries also in USA, Canada, and Israel in 1994, 1998, 2002, and 2006. Objective. The aim of this study was to analyze features and trends in alcohol consumption among the samples of 11-, 13-, and 15-year-old adolescents (school-aged children) in Lithuania during 1994–2006. Material and methods. Representative sampl
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15

Telfer, Paul, Banu Kaya, Dimitris A. Tsitsikas, Filipa Barroso, and Cynthia Sangarappillai. "Hydroxyurea Therapy Does Not Impact Current Survival Estimates in the East London Sickle Cell Newborn Cohort Study." Blood 132, Supplement 1 (2018): 3655. http://dx.doi.org/10.1182/blood-2018-99-116544.

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Abstract Background: There is a lack of data to estimate current life expectancy in adults who have had continual access to best standard of care since birth. Furthermore, the effect of disease-modifying treatments on survival has not been adequately evaluated. Data from the East London Newborn Cohort Study provide information on these outcomes in the setting of the UK National Health Service. Methods: Inclusion criteria were birth in the London boroughs of Hackney and Tower Hamlets, diagnosis by newborn screening (local programme from 1983 to 2004, and national programme from 2004 onwards), r
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16

Ravens-Sieberer, U., and V. Ottova. "Kinder- und Jugendgesundheit in Deutschland: Erkenntnisse aus der Health Behaviour in School-aged Children (HBSC)-WHO-Jugendgesundheitsstudie 2002-2010." Das Gesundheitswesen 74, S 01 (2012): S4—S7. http://dx.doi.org/10.1055/s-0032-1316340.

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17

Kopcakova, Jaroslava, Zuzana Dankulincova Veselska, Michal Kalman, et al. "Test–Retest Reliability of a Questionnaire on Motives for Physical Activity among Adolescents." International Journal of Environmental Research and Public Health 17, no. 20 (2020): 7551. http://dx.doi.org/10.3390/ijerph17207551.

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The aim of this study was to investigate the test–retest reliability of the motives for undertaking physical activity (PA) items from the Health Behavior in School-Aged Children (HBSC) study questionnaire among Slovak and Czech adolescents and to determine whether this reliability differs by gender, age group and country. We obtained data from 580 students aged 11 and 15 years old (51.2% boys) who participated in a test and retest study with a four-week interval in 2013 via the Health Behavior in School-Aged Children cross-sectional study in the Czech Republic and Slovakia. We estimated the te
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18

Kleszczewska, Dorota, Joanna Mazur, Jens Bucksch, Anna Dzielska, Catherina Brindley, and Agnieszka Michalska. "Active Transport to School May Reduce Psychosomatic Symptoms in School-Aged Children: Data from Nine Countries." International Journal of Environmental Research and Public Health 17, no. 23 (2020): 8709. http://dx.doi.org/10.3390/ijerph17238709.

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It is widely proven that being physically active and avoiding sedentary behaviour help to improve adolescents’ well-being and keep them in better health in general. We aimed to investigate the relationship between modes of transport to school and subjective complaints among schoolchildren. Analyses were based on the HBSC (Health Behaviour in School-aged Children) surveys conducted in 2017/18 in nine countries (N = 55,607; mean age 13.43 ± 1.64 yrs.). The main outcome showed that health complaints consisted of somatic and psychological complaints. Transport to school was characterized by mode o
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19

Repka, T., O. Shalev, R. Reddy, et al. "Nonrandom association of free iron with membranes of sickle and beta- thalassemic erythrocytes." Blood 82, no. 10 (1993): 3204–10. http://dx.doi.org/10.1182/blood.v82.10.3204.3204.

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Abstract To further define the nature of abnormal iron deposits on the membranes of pathologic red blood cells, we have used sickle cell anemia (HbSS), HbSC, and beta-thalassemic erythrocytes (RBCs) to prepare inside-out membranes (IOM) and insoluble membrane aggregates (AGGs) containing coclustered hemichrome and band 3. Study of IOM from HbSC and thalassemic patients showed that amounts of heme iron and, especially, free iron were much higher in patients who had undergone surgical splenectomy. The membrane AGGs from HbSS and beta-thalassemic RBCs contained much more globin than heme, with th
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20

Repka, T., O. Shalev, R. Reddy, et al. "Nonrandom association of free iron with membranes of sickle and beta- thalassemic erythrocytes." Blood 82, no. 10 (1993): 3204–10. http://dx.doi.org/10.1182/blood.v82.10.3204.bloodjournal82103204.

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To further define the nature of abnormal iron deposits on the membranes of pathologic red blood cells, we have used sickle cell anemia (HbSS), HbSC, and beta-thalassemic erythrocytes (RBCs) to prepare inside-out membranes (IOM) and insoluble membrane aggregates (AGGs) containing coclustered hemichrome and band 3. Study of IOM from HbSC and thalassemic patients showed that amounts of heme iron and, especially, free iron were much higher in patients who had undergone surgical splenectomy. The membrane AGGs from HbSS and beta-thalassemic RBCs contained much more globin than heme, with this discre
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21

Ren, Ghebremeskel, Okpala, Lee, Ibegbulam, and Crawford. "Patients with Sickle Cell Disease have Reduced Blood Antioxidant Protection." International Journal for Vitamin and Nutrition Research 78, no. 3 (2008): 139–47. http://dx.doi.org/10.1024/0300-9831.78.3.139.

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In previous studies, we found that homozygous sickle cell (HbSS) patients, compared with their healthy (HbAA) counterparts, had reduced levels of the omega-3 fatty acids, eicosapentaenoic (EPA) and docosahexaenoic (DHA) acids, in red cells, platelets, and mononuclear cells. These differences were not due to lower intake of the two fatty acids. We have investigated whether reduced antioxidant status in the patients could help explain the observed phenomenon. Blood specimens previously obtained for fatty acid study from Nigerian (26 HbSS and 30 HbAA) and British (30 HbSS, 9 sickle cell-hemoglobi
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22

Currie, Candace, Saoirse Nic Gabhainn, and Emmanuelle Godeau. "The Health Behaviour in School-aged Children: WHO Collaborative Cross-National (HBSC) Study: origins, concept, history and development 1982–2008." International Journal of Public Health 54, S2 (2009): 131–39. http://dx.doi.org/10.1007/s00038-009-5404-x.

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23

Schimmel, Marein, Erfan Nur, Sacha Zeerleder, et al. "Increased Circulating Nucleosomes and Neutrophil Activation As a Measure of the Formation of Neutrophil Extracellular Traps (NETs) During Sickle Cell Painful Crisis." Blood 120, no. 21 (2012): 821. http://dx.doi.org/10.1182/blood.v120.21.821.821.

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Abstract Abstract 821 Introduction: Sickle cell disease (SCD) is characterized by recurrent acute vaso-occlusive painful crisis frequently leading to SCD related complications such as acute chest syndrome, stroke, multi-organ failure and even sudden death. The complex pathophysiology of the vaso-occlusive painful crisis is mediated by activation of endothelial cells, adhesion of sickled erythrocytes and neutrophils, oxidative stress, coagulation activation and increased release of inflammatory mediators, resulting in ischemic organ damage. Recently, neutrophils have been demonstrated to form n
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24

Grotto, Helena Zerlotti Wolf, Elza Miyuki Kimura, and Márcia Victor Carneiro. "Soluble transferrin receptor in sickle cell diseases: correlation with spleen function." Sao Paulo Medical Journal 117, no. 4 (1999): 145–50. http://dx.doi.org/10.1590/s1516-31801999000400002.

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OBJECTIVE: To correlate spleen function with soluble transferrin receptor (sTfR) levels and red cell ferritin (RCF) values in patients with sickle cell diseases. DESIGN: Prospective study. LOCATION: University Hospital, School of Medical Sciences, State University of Campinas; a tertiary hospital. PARTICIPANTS: 60 patients with sickle cell diseases, in a steady state, who had not received blood transfusions for 3 months; 28 normal individuals with no clinical or laboratory signs of anemia. MEASUREMENTS: Determination of serum iron, transferrin iron-binding capacity, serum ferritin, RCF and sTf
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25

Booth, M. L. "The reliability and validity of the physical activity questions in the WHO health behaviour in schoolchildren (HBSC) survey: a population study." British Journal of Sports Medicine 35, no. 4 (2001): 263–67. http://dx.doi.org/10.1136/bjsm.35.4.263.

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26

Gupta, A., C. M. Davison, and M. A. McIsaac. "Masking in reports of “most serious” events: bias in estimators of sports injury incidence in Canadian children." Health Promotion and Chronic Disease Prevention in Canada 36, no. 8 (2016): 143–48. http://dx.doi.org/10.24095/hpcdp.36.8.01.

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Introduction Surveys that collect information on injuries often focus on the single “most serious” event to help limit recall error and reduce survey length. However, this can mask less serious injuries and result in biased incidence estimates for specific injury subcategories. Methods Data from the 2002 Health Behaviour in School-aged Children (HBSC) survey and from the Canadian Hospitals Injury Reporting and Prevention Program (CHIRPP) were used to compare estimates of sports injury incidence in Canadian children. Results HBSC data indicate that 6.7% of children report sustaining a sports in
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Veselska, Zuzana Dankulincova, Daniela Husarova, and Michaela Kosticova. "Energy Drinks Consumption Associated with Emotional and Behavioural Problems via Lack of Sleep and Skipped Breakfast among Adolescents." International Journal of Environmental Research and Public Health 18, no. 11 (2021): 6055. http://dx.doi.org/10.3390/ijerph18116055.

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The aim of our study was to explore whether energy drink consumption is associated with both emotional and behavioural problems and whether this association might be mediated by amount of sleep and breakfast consumption among adolescents. The nationally representative Health Behaviour in School-aged Children (HBSC) study, realised in 2018 in Slovakia in schools, was used to acquire needed data, with the research sample of 8405 adolescents from 11 to 15 years old (mean age = 13.43; 50.9% boys) who completed the questionnaires on their own in a presence of researchers and research assistants. Em
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Thomas-Dewing, Rowena R., John Chambers, Nicholas Hart, and Jo Howard. "A Comparison of Echocardiogram Screening for Pulmonary Hypertension in Asymptomatic and Symptomatic Patients with Sickle Cell Disease." Blood 112, no. 11 (2008): 4801. http://dx.doi.org/10.1182/blood.v112.11.4801.4801.

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Abstract Background: Pulmonary hypertension (PHT) is an increasingly recognised complication of sickle cell disease (SCD), even in asymptomatic patients. Studies from the US have shown a prevalence of PHT of between 20–30% and this has been associated with an increased mortality. The prevalence of PHT in the UK sickle cell disease population is unknown. Method: We identified adult patients with a diagnosis of SCD (HbSS, HbSC, HbSB0thalassaemia and HbSB+ thalassaemia) who had screening for PHT using transthoracic echocardiography over a one year period. We compared the echocardiographic finding
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29

Molcho, Michal, Aoife Gavin, and Devon Goodwin. "Levels of Physical Activity and Mental Health in Adolescents in Ireland." International Journal of Environmental Research and Public Health 18, no. 4 (2021): 1713. http://dx.doi.org/10.3390/ijerph18041713.

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The benefits of physical activity for the physical health of individuals are well documented. Less is known about the benefits of physical activity for mental health. This paper explores the associations between physical activity and positive mental health and mental health problems. The paper utilises data collected from a representative sample of 10–17-year-old adolescents in Ireland. Physical activity in the study is measured using moderate-to-vigorous physical activity (MVPA) and vigorous physical activity (VPA). Mental health was measured using the Cantril Leader of Life Satisfaction, the
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Herbst, John, Tyler Crissinger, and Kelly Baldwin. "Diffuse Ischemic Strokes and Sickle Cell Crisis Induced by Disseminated Anaplasmosis: A Case Report." Case Reports in Neurology 11, no. 3 (2019): 271–76. http://dx.doi.org/10.1159/000502567.

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We present a 26-year-old female with HbSC disease who presented to the emergency department multiple times with pain and shortness of breath, eventually developing unresponsiveness and a brief episode of pulseless electrical activity. She was admitted to the intensive care unit with multisystem organ failure and found to have diffuse ischemic strokes. Infectious workup revealed disseminated anaplasmosis and babesiosis, which had likely caused sickle cell crisis, atypical hemolytic-uremic syndrome, and ischemic brain injury. She was started on eculizumab therapy as well as antimicrobial therapy
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García-Moya, Irene, Antonia Jiménez-Iglesias, and Carmen Moreno. "The Contribution from Relationships with Parents and Teachers to the Adolescent Sense of Coherence." YOUNG 25, no. 4 (2016): 391–406. http://dx.doi.org/10.1177/1103308816646672.

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Sense of coherence (SOC) is receiving increasing attention from a number of disciplines interested in the study of adolescent positive development. Given the significant links between SOC and well-being, attention is now moving to the precursors of SOC. The aim of this study was to analyze the contribution of relationships with parents and teachers (contextual factors) to young people’s SOC while taking into account the potential role of individual differences in prosociality and hyperactivity-inattention (individual factors). The sample consisted of 2,979 adolescents aged 15–18 who had partic
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Kuntsche, Emmanuel, Mary Overpeck, and Lorenza Dallago. "Television Viewing, Computer Use, and a Hostile Perception of Classmates Among Adolescents From 34 Countries." Swiss Journal of Psychology 67, no. 2 (2008): 97–106. http://dx.doi.org/10.1024/1421-0185.67.2.97.

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The present study investigated the relationship between adolescents’ perception of a lack of classmate support and their individual and their respective culture’s daily amounts of television viewing and computer use. We tested multilevel regression models based on data from the responses of 150 552 adolescents aged 11, 13, and 15 years from 34 cultures who participated in the 2001-2002 Health Behavior in School-Aged Children (HBSC) survey. Results revealed that the average amount of television viewing in the respective adolescents’ culture explained variation in their perception of a lack of c
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Drasar, Emma, Sarah A. Bennett, Nisha Vasavda, and Swee Lay Thein. "Predictors of Length of Stay and Time to Readmission in Adult Patients with Sickle Cell Disease: A Single Institution Experience in the UK." Blood 118, no. 21 (2011): 2130. http://dx.doi.org/10.1182/blood.v118.21.2130.2130.

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Abstract Abstract 2130 Background: Sickle cell disease (SCD) is characterised by chronic hemolytic anemia and recurrent acute clinical events. The most common cause of hospital attendance is acute pain and in our patient population it accounts for 84% of all admissions. Financial pressure has led to an interest in the factors affecting length of stay (LOS) and readmission rate (RAR). The 30 day RAR has been highlighted by the UK government as a care standard. In the UK general hospital population the 30 day RAR is 6.5% of all admissions with an estimated cost to the NHS of £1.6 billion/year. A
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34

Smith, Otto R. F., Ole Melkevik, Oddrun Samdal, Torill M. Larsen, and Ellen Haug. "Psychometric properties of the five-item version of the Mindful Awareness Attention Scale (MAAS) in Norwegian adolescents." Scandinavian Journal of Public Health 45, no. 4 (2017): 373–80. http://dx.doi.org/10.1177/1403494817699321.

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Objectives: The aim of the present study was to examine the factor structure, model-based reliability, measurement invariance and concurrent validity of the five-item version of the Mindfulness Attention Awareness Scale (MAAS) in Norwegian adolescents. Methods: An initial pilot study was carried out using a sample of 77 fifteen year olds. For the main analyses, a sample of 2140 Norwegian adolescents was used who participated in the cross-sectional Health Behaviour in School-Aged Children (HBSC) study. All participants were asked to complete a questionnaire. Results: Confirmatory factor analyse
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Bronté-Hall, Lanetta, Matthew Parkin, Courtney Green, et al. "Real-World Clinical Burden of Sickle Cell Disease in the US Community-Practice Setting: A Single-Center Experience from the Foundation for Sickle Cell Disease Research." Blood 134, Supplement_1 (2019): 5856. http://dx.doi.org/10.1182/blood-2019-128700.

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Background Sickle cell disease (SCD) is a progressively debilitating monogenic disease characterized by unpredictable, acute, life-threatening episodes and chronic complications such as hemolytic anemia and end-organ damage. It presents with a range of severity resulting in significant morbidity, poor quality of life, and early mortality. Real-world data on treatments and clinical outcomes for patients (pts) with SCD are limited, particularly in the community clinical care setting. The objectives of this retrospective real-world study were to characterize clinical manifestations and management
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Jildeh, Christine, Ziad Abdeen, Haleama Al Sabbah, et al. "Labor and Related Injuries among Schoolchildren in Palestine: Findings from the National Study of Palestinian Schoolchildren (HBSC-WBG2006)." ISRN Pediatrics 2014 (April 3, 2014): 1–11. http://dx.doi.org/10.1155/2014/729573.

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Background. Labor related injuries among Palestinian schoolchildren are a significant undocumented public health concern. This study aimed at documenting the prevalence and nature of work related injuries among schoolchildren as well as identifying sociodemographic factors that predict these injuries. Methods. A cross-sectional survey included 15,963 children of whom 6458 (40.8%) completed an optional package related to labor. Students aged 12–18 years self-completed the international WHO collaborative HBSC valid questionnaires between April and May of 2006. Results. Approximately 73.8% of the
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Strózik, Dorota, and Tomasz Strózik. "Spatial Differentiation of Child Well-Being in Europe." Folia Oeconomica Stetinensia 14, no. 1 (2014): 78–90. http://dx.doi.org/10.2478/foli-2014-0106.

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Abstract An important determinant of the level of development of each country and the whole Europe is the care about an adequate level of well-being and quality of life of all citizens, above all those to whom the future belongs - our children. In the times of demographic changes it is particularly important to understand specific needs and rights of the youngest generation of Europeans. Investing in children is investing in our future, the shape of which will depend precisely on whether the youngest generation will be healthy, well educated and able to participate in the development of their
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Arends, Samuel, Jan Adriaan Coebergh, Jean Louis Kerkhoffs, Adrianus van Gils, and Hille Koppen. "Severe unilateral headache caused by skull bone infarction with epidural haematoma in a patient with sickle cell disease." Cephalalgia 31, no. 12 (2011): 1325–28. http://dx.doi.org/10.1177/0333102411414441.

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Background: The clinical manifestations of sickle cell disease (SCD) vary, but may be attributed to vaso-occlusion, chronic hemolytic anemia, and infections as a result of functional asplenia. We report a case of a man who presented with severe headache caused by an uncommon complication of SCD. Case: A 19-year-old Surinamer man presented to the emergency department with severe headache. The progressive headache started one day previously. The headache was located frontotemporally on the right side. It was pulsating with paroxysms of fierce pain. There was no nausea or vomiting. The medical hi
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Thomson, C. "Changes in HIV/AIDS education, knowledge and attitudes among Scottish 1516 year olds, 19901994: findings from the WHO: Health Behaviour in School-aged Children Study (HBSC)." Health Education Research 14, no. 3 (1999): 357–70. http://dx.doi.org/10.1093/her/14.3.357.

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Molcho, M., Y. Harel, W. Pickett, et al. "The epidemiology of non-fatal injuries among 11-, 13- and 15-year old youth in 11 countries: findings from the 1998 WHO-HBSC cross national survey." International Journal of Injury Control and Safety Promotion 13, no. 4 (2006): 205–11. http://dx.doi.org/10.1080/17457300600864421.

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Haug, Ellen, Mette Rasmussen, Oddrun Samdal, et al. "Overweight in school-aged children and its relationship with demographic and lifestyle factors: results from the WHO-Collaborative Health Behaviour in School-aged Children (HBSC) Study." International Journal of Public Health 54, S2 (2009): 167–79. http://dx.doi.org/10.1007/s00038-009-5408-6.

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Šumskas, Linas, Ilona Lenčiauskienė, and Apolinaras Zaborskis. "Health behavior inequalities among Lithuanian, Polish and Russian school-aged children in Lithuania." Open Medicine 5, no. 1 (2010): 97–107. http://dx.doi.org/10.2478/s11536-009-0108-4.

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AbstractThe aim of this study was to compare and get a deeper insight into issues of the health and health behavior inequalities among Lithuanian, Polish and Russian school-aged children in national and international contexts. Investigations were carried out in the framework of Health Behavior in School-aged Children (HBSC) study — a WHO collaborative cross-national survey. Five thousand seven hundred and seventy six randomly selected students aged 11, 13, and 15 years of age answered questionnaires in the classroom in 108 schools located in different regions in Lithuania in March–April of 200
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van Tuijn, Charlotte F. J., Marein Schimmel, Eduard J. van Beers, and Bart J. Biemond. "Systematic Evaluation Of Chronic Organ Damage In Adult Sickle Cell Patients. A Seven-Year Follow-Up Study." Blood 122, no. 21 (2013): 4683. http://dx.doi.org/10.1182/blood.v122.21.4683.4683.

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Introduction The occurrence of organ damage in sickle cell disease (SCD) is a crucial determinant for both medical treatment and prognosis. In a previous study, we systematically analyzed the prevalence of SCD related organ damage and complications in adult sickle cell patients in a tertiary teaching hospital in the Netherlands. We now describe a seven-year follow-up of this patient cohort, to provide an insight into the course of the various forms of organ damage and SCD related complications. Methods At baseline in 2006, 110 adult patients visiting the outpatient clinic of our hospital were
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Heidmets, L., A. Samm, M. Sisask, K. Kõlves, K. Aasvee, and A. Värnik. "Sexual Behavior, Depressive Feelings, and Suicidality Among Estonian School Children Aged 13 to 15 Years." Crisis 31, no. 3 (2010): 128–36. http://dx.doi.org/10.1027/0227-5910/a000011.

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Background: The present paper is based on a WHO Collaborative Cross-National Study “Health Behavior in School-Aged Children (HBSC).” Aims: It aimed at describing and analyzing how the sexual behaviors of 13- to 15-year-old Estonian school children were associated with self-reported depressive feelings and suicidality. Distinctive behavioral traits in relation to age of first sexual intercourse were also investigated. Methods: Self-reported questionnaires from school children (n = 3,055) were analyzed. Results: In total, 15.2% of school children reported being nonvirgin. Among 13-year-olds, 2.9
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Költő, András, Alina Cosma, Honor Young, et al. "Romantic Attraction and Substance Use in 15-Year-Old Adolescents from Eight European Countries." International Journal of Environmental Research and Public Health 16, no. 17 (2019): 3063. http://dx.doi.org/10.3390/ijerph16173063.

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Sexual minority youth are at higher risk of substance use than heterosexual youth. However, most evidence in this area is from North America, and it is unclear whether the findings can be generalized to other cultures and countries. In this investigation, we used data from the 2014 Health Behaviour in School-aged Children (HBSC) study to compare substance use in same- and both-gender attracted 15-year-old adolescents from eight European countries (n = 14,545) to that of their peers who reported opposite-gender attraction or have not been romantically attracted to anyone. Both-gender attracted,
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Kavaliauskienė, Aistė, Antanas Šidlauskas, and Apolinaras Zaborskis. "Demographic and social inequalities in need for orthodontic treatment among schoolchildren in Lithuania." Medicina 46, no. 11 (2010): 767. http://dx.doi.org/10.3390/medicina46110108.

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The present study, which focused on Lithuanian 11–15-year-old schoolchildren, was aimed to describe the frequency of orthodontic anomalies in terms of self-reported complaints about malposed teeth and malocclusion and self-reported use of orthodontic appliances (removable or braces) across different sociodemographic strata. Material and methods. The study population comprised 5632 schoolchildren surveyed in the 2005-2006 school year according to the WHO collaborative cross-national HBSC study in Lithuania. Results. Almost half (47.5%) of schoolchildren reported orthodontic complaints. Therefor
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Zaborskis, Apolinaras, Linas Šumskas, Nida Žemaitienė, Vilius Grabauskas, Aurelijus Veryga, and Robertas Petkevičius. "Trends of smoking prevalence among Lithuanian school-aged children in 1994–2006." Medicina 45, no. 10 (2009): 798. http://dx.doi.org/10.3390/medicina45100104.

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Background. Despite much effort spent on antismoking programs in schools in different countries, limited effects have been observed in many cases. Evidence from European countries shows that active tobacco control actions such as ban on tobacco advertising, increase of tobacco taxes could lead to successful results. Our study was aimed to analyze time trends on smoking in Lithuanian school-aged children during the period of 1994–2006 in the context of antismoking policies, which were implemented in Lithuania. Material and methods. This study was a part of WHO Cross-National Health Behavior in
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Awaitey, Daniel Kpodji, Elliot Elikplim Akorsu, Emmanuel Allote Allotey, et al. "Assessment of Hemoglobin Variants in Patients Receiving Health Care at the Ho Teaching Hospital: A Three-Year Retrospective Study." Advances in Hematology 2020 (March 21, 2020): 1–6. http://dx.doi.org/10.1155/2020/7369731.

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Background. It is estimated that one out of every three Ghanaians has hemoglobin genotype mutation. This change in genetic make-up may result in genotypes such as HbAS, HbSS, and HbSC. Many children in low- and middle-income countries die even before they are diagnosed with sickle cell disease (SCD). In Africa, there are limited data on the incidence and prevalence of SCD and the Volta region of Ghana is no exception. Aim. The aim of this study was to determine the prevalence of SCD and to assess the hemoglobin variants among patients attending Ho Teaching Hospital. Methods. A retrospective st
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Ragg, Susanne, Melissa Key, Fernanda Rankin, and Monica L. Hulbert. "Insights from Comparative Serum Proteomic Profiling of Children with Sickle Cell Disease: The Effect of Hydroxyurea and Genotype on Protein Abundance." Blood 128, no. 22 (2016): 1302. http://dx.doi.org/10.1182/blood.v128.22.1302.1302.

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Abstract Introduction: Sickle cell disease (SCD) is a multisystem disease, with substantial variation in presentation and clinical course. Many protein biomarkers have been described in serum and plasma of children with homozygous sickle cell disease. In order to understand the effect of hydroxyurea and the hemoglobin SC genotype on serum protein levels, we compared the relative abundance of serum proteins in healthy children and children with SCD. Methods: The relative concentration of 140 different serum proteins was measured using liquid chromatography tandem mass spectrometry. Serum sample
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Okpala, Iheanyi, Hongmei Ren, Obi Ibegbulam, Keb Ghebremeskel, Cynthia Ugochukwu, and Michael Crawford. "Omega-3 Fatty Acid Deficiency in Sickle Cell Disease Correlates with Clinical Severity and Has Therapeutic Implications." Blood 110, no. 11 (2007): 3781. http://dx.doi.org/10.1182/blood.v110.11.3781.3781.

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Abstract Background: Clinical illness in SCD results not only from the β-globin gene mutation, but also from other genetic and environmental factors acting in concert. The biological basis of individual variation in the severity of SCD is not fully understood. Our previous study revealed that WBCs from people with severe SCD express high levels of the adhesion molecules L-selectin (CD62L) and αMβ2 integrin (CD11a/18) in steady state. These cell membrane proteins mediate leukocyte adherence to vascular endothelium and facilitate vaso-occlusion: a fundamental pathological process in SCD. The lip
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