FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2258554865> ?p ?o ?g. }

• W2258554865 abstract "Background; sickle cell means an abnormal crescent shaped red blood cell. The present study aimed to evaluate an educational program for the mothers and their children including the knowledge and practices needed in dealing with the sickle cell disease and assessment of pain severity before and after the educational program. This study followed a quasi- experimental design. The sample was consist of 50 children suffering from sickle cell disease and their mothers who were attending at Pediatric Hematology and Oncology unit of Tanta University Hospital and Inpatient Pediatric Department of Elhoboor Hospital in Khafer Al-Sheik. Three tools were used for data collection: a structured interview sheet , pain assessment tool, and mothers and their children knowledge Questionnaire. The result revealed that 60% of children with sickle cell disease had a mean age of 12.1±4.02 years. Before program application the total scores of knowledge for mothers are fair and poor with percentage 14% and 43% respectively, whereas immediately and after three months of the program application the total score of knowledge for all mothers is good. There was significant positive impact on total score of the knowledge about sickle cell disease. There was a highly significant positive impact of Quran program on total score of pain severity. Conclusion: the study was found that the three programs of non pharmacological methods (Quran, progressive relaxation and yoga) reduce severity of pain respectively. There was highly improvement of mothers' knowledge immediately, and after three month the application of program. This study recommended: informing parents about non-pharmacological therapies for pain, such as, progressive relaxation and massage. to recurrent painful episodes called sickle cell crises. (1) The prevalence of sickle cell anemia, are globally widespread. About 5% of the world ' s population carries genes responsible for haemoglobinopathies. (2) The first case of sickle cell anemia in Egypt was reported in 1951 by Abbasy (3) sickle cell disease was recorded in Pediatric Hematology and Oncology unit of University Hospital in Tanta that 1(2%) as homozygous sickle cell (HBSS), 3(6%) as compound heterozygous state of sickle cell (SS), 2(4%) as sickle cell B. Thalassemia , 1(2%) as sickle cell hemoglobin C disease (HbSC). ( 4) Sickle cell anemia is caused by a mutation in the gene that tells the body to make hemoglobin. The red cells, iron rich compound that gives blood its red color. Hemoglobin allows red blood cells to carry oxygen from the lung to all parts of the body. In sickle cell anemia the abnormal hemoglobin causes red blood cells to become rigid, sticky and misshaped, also the sickle cell gene is passed from generation to generation in pattern of inheritance called autosomal receive inheritance. This means that both the mother and father must pass the defective from of the gene to the child to be affected. (5) Sickle cell anemia covers a wide spectrum of illness. Most affected children have chronic anemia with a hemoglobin concentration of around 8 g/dl. The main problems arise from the tendency of the red blood cells to become sickle shaped and block capillaries at low oxygen tension. In children, sickle shaped red blood cells often become trapped in the spleen, leading to a serious risk of death before the age of seven years from a sudden profound anemia associated with rapid splenic enlargement or because lack of splenic function that permits an overwhelming infection. Between 6 and 18 months of age the affect children most often present with painful swelling of the hands or feet (hand -feet syndrome). Children may also suffer recurrent and" @default.
• W2258554865 created "2016-06-24" @default.
• W2258554865 creator A5001032083 @default.
• W2258554865 creator A5044201672 @default.
• W2258554865 creator A5058620822 @default.
• W2258554865 creator A5061535812 @default.
• W2258554865 creator A5070171062 @default.
• W2258554865 creator A5077443645 @default.
• W2258554865 date "2015-11-16" @default.
• W2258554865 modified "2023-09-27" @default.
• W2258554865 title "Effect of Upgrading Maternal Concepts and Skills on Reducing Pain Severity of their Children Suffering From Sickle Cell Disease" @default.
• W2258554865 cites W1582580881 @default.
• W2258554865 cites W1980583777 @default.
• W2258554865 cites W2000340719 @default.
• W2258554865 cites W2003136627 @default.
• W2258554865 cites W2040790160 @default.
• W2258554865 cites W2042817873 @default.
• W2258554865 cites W2047851828 @default.
• W2258554865 cites W2050262436 @default.
• W2258554865 cites W2053124374 @default.
• W2258554865 cites W2058243130 @default.
• W2258554865 cites W2062418287 @default.
• W2258554865 cites W2064654252 @default.
• W2258554865 cites W2080150622 @default.
• W2258554865 cites W2109521235 @default.
• W2258554865 cites W2150182456 @default.
• W2258554865 cites W2151443812 @default.
• W2258554865 cites W2184599232 @default.
• W2258554865 cites W2185442637 @default.
• W2258554865 cites W2322074970 @default.
• W2258554865 cites W2339872102 @default.
• W2258554865 cites W2408317078 @default.
• W2258554865 cites W2487881811 @default.
• W2258554865 cites W3210005698 @default.
• W2258554865 cites W59714281 @default.
• W2258554865 cites W650663168 @default.
• W2258554865 doi "https://doi.org/10.6084/m9.figshare.1603384.v1" @default.
• W2258554865 hasPublicationYear "2015" @default.
• W2258554865 type Work @default.
• W2258554865 sameAs 2258554865 @default.
• W2258554865 citedByCount "0" @default.
• W2258554865 crossrefType "journal-article" @default.
• W2258554865 hasAuthorship W2258554865A5001032083 @default.
• W2258554865 hasAuthorship W2258554865A5044201672 @default.
• W2258554865 hasAuthorship W2258554865A5058620822 @default.
• W2258554865 hasAuthorship W2258554865A5061535812 @default.
• W2258554865 hasAuthorship W2258554865A5070171062 @default.
• W2258554865 hasAuthorship W2258554865A5077443645 @default.
• W2258554865 hasConcept C126322002 @default.
• W2258554865 hasConcept C1862650 @default.
• W2258554865 hasConcept C187212893 @default.
• W2258554865 hasConcept C2779134260 @default.
• W2258554865 hasConcept C71924100 @default.
• W2258554865 hasConceptScore W2258554865C126322002 @default.
• W2258554865 hasConceptScore W2258554865C1862650 @default.
• W2258554865 hasConceptScore W2258554865C187212893 @default.
• W2258554865 hasConceptScore W2258554865C2779134260 @default.
• W2258554865 hasConceptScore W2258554865C71924100 @default.
• W2258554865 hasLocation W22585548651 @default.
• W2258554865 hasOpenAccess W2258554865 @default.
• W2258554865 hasPrimaryLocation W22585548651 @default.
• W2258554865 hasRelatedWork W1598141473 @default.
• W2258554865 hasRelatedWork W1775086456 @default.
• W2258554865 hasRelatedWork W1877982447 @default.
• W2258554865 hasRelatedWork W1969287391 @default.
• W2258554865 hasRelatedWork W2000934279 @default.
• W2258554865 hasRelatedWork W2011178759 @default.
• W2258554865 hasRelatedWork W2091771886 @default.
• W2258554865 hasRelatedWork W2169598619 @default.
• W2258554865 hasRelatedWork W2190675496 @default.
• W2258554865 hasRelatedWork W2300486054 @default.
• W2258554865 hasRelatedWork W2327717925 @default.
• W2258554865 hasRelatedWork W2331629725 @default.
• W2258554865 hasRelatedWork W2342128532 @default.
• W2258554865 hasRelatedWork W2523644851 @default.
• W2258554865 hasRelatedWork W2617452447 @default.
• W2258554865 hasRelatedWork W2782510043 @default.
• W2258554865 hasRelatedWork W2982567563 @default.
• W2258554865 hasRelatedWork W49892557 @default.
• W2258554865 hasRelatedWork W1626917236 @default.
• W2258554865 hasRelatedWork W2251837259 @default.
• W2258554865 isParatext "false" @default.
• W2258554865 isRetracted "false" @default.
• W2258554865 magId "2258554865" @default.
• W2258554865 workType "article" @default.