Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/346560
Full metadata record
DC FieldValueLanguage
dc.coverage.spatial
dc.date.accessioned2021-11-02T04:41:05Z-
dc.date.available2021-11-02T04:41:05Z-
dc.identifier.urihttp://hdl.handle.net/10603/346560-
dc.description.abstractSickle cell diseases (SCDs) is an emerging public health challenge, not only in India but also globally. It has been estimated that, between 2010 and 2050, about 14.2 million babies will be born with sickle cell disease (SCD). According to ICMR survey Sickle Cell gene, India has a very huge population of tribal community about 18 crore and expected to have 1.80 crore Sickle Cell Trait and 14 lakhs of Sickle Cell Disease. ICMR took initiative in the year 1987 and again in 1999, to quantify the burden of Sickle cell gene in India through its multi centric project. Sickle Cell gene is found amongst different tribal groups of India, and prevalence rate varies from 5 to 34% and primitive tribes of south of Gujarat, viz; Kolcha, Kotwadia and Kathodi; 30 % of Sickle Cell Disease children die before they reach adulthood and the remaining 70 % die by the age of 50. newlineGujarat Sickle cell Society has stated that among 89.12 lakh tribal population at least 9,00,000 population were having Sickle Cell Trait and 70,000 were suffering with Sickle Cell Disease. According to WHO,10% of Sickle Cell Disease patients die by the age of one year and in many sub-Saharan countries mortality is much higher than that. newlineThis disease has not gained much concern at national as well as state level. Screening is not a common practice and the diagnosis is usually made when a patient presents with severe complications. Patients affected by SCD are frequently misdiagnosed and mistreated as most common iron deficiency (nutritional) anaemia with iron therapy. The primary need of this study is to establish network for filling up the gap of ignorance about Sickle cell disease among tribal community and increasing the awareness for sickle cell disease. The family counselling session is needed to help in capacity building of family members for delivering necessary care. newline newline
dc.format.extentxxiii,193p
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titlestudy to assess the effectiveness of Multifactorial Nursing Intervention on knowledge Clinical Features and Quality of life among adults diagnosed with sickle cell disease from tribal community Surat
dc.title.alternative
dc.creator.researcherSuchismita Bhowmik
dc.subject.keywordClinical Medicine
dc.subject.keywordCommunity Health Nursing
dc.subject.keywordMedicine Research and Experimental sickle cell disease
dc.description.note
dc.contributor.guideShetty Rani
dc.publisher.placeBarodli
dc.publisher.universityUka Tarsadia University
dc.publisher.institutionFaculty of Medical and Paramedical
dc.date.registered2018
dc.date.completed2021
dc.date.awarded2021
dc.format.dimensions
dc.format.accompanyingmaterialCD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Faculty of Medical and Paramedical

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File508.52 kBAdobe PDFView/Open
02_certificates.pdf1.6 MBAdobe PDFView/Open
03_preliminary pages.pdf524.9 kBAdobe PDFView/Open
04_chapter 1.pdf1.19 MBAdobe PDFView/Open
05_chapter 2.pdf88.57 kBAdobe PDFView/Open
06_chapter 3.pdf693.74 kBAdobe PDFView/Open
07_chapter 4.pdf1.57 MBAdobe PDFView/Open
08_chapter 5.pdf955.45 kBAdobe PDFView/Open
09_ chapter 6.pdf718.97 kBAdobe PDFView/Open
10_ chapter 7.pdf521.25 kBAdobe PDFView/Open
11_references.pdf536.03 kBAdobe PDFView/Open
12_appendices.pdf2.54 MBAdobe PDFView/Open
12_plagiarism report.pdf407.4 kBAdobe PDFView/Open
13_list of publication.pdf1.45 MBAdobe PDFView/Open
80_recommendation.pdf160.65 kBAdobe PDFView/Open


Items in Shodhganga are licensed under Creative Commons Licence Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0).

Altmetric Badge: