Thalassemia in Children and Adolescents : (Record no. 163742)

MARC details
000 -LEADER
fixed length control field 04998nam a2200433Ia 4500
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - أخر تعامل مع التسجيلة
control field 20260616114928.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 2310s2022 ua a frm 000 0 und d
040 ## - CATALOGING SOURCE
Original cataloguing agency EG-EULC
Language of cataloging eng
Transcribing agency EG-EULC
Modifying agency EG-EULC
Description conventions rda
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title eng
Language code of summary or abstract eng
-- ara
049 ## - Acquisition Source
Acquisition Source Deposit
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 618.976152
092 ## - LOCALLY ASSIGNED DEWEY CALL NUMBER (OCLC)
Classification number 618.976152
Edition number 21
097 ## - Degree
Degree M.Sc
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Local Call Number Cai01.11.28.M.Sc.2022.Me.T
100 ## - MAIN ENTRY--PERSONAL NAME
Authority record control number or standard number Merna Safwat fekry Philobos
Preparation preparation.
245 ## - TITLE STATEMENT
Title Thalassemia in Children and Adolescents :
Remainder of title a single center study of adherence to evidence based management guidelines and practice obstacles /
Statement of responsibility, etc. by Merna Safwat fekry Philobos ; Supervisors Prof.Dr.Eman Abdel-Raouf Mohamed abd Elal, Prof.Dr.Niveen Mohamed Salama, Prof.Dr.Amera Mohammed Hasnoon.
246 ## - VARYING FORM OF TITLE
Title proper/short title دراسة فردية مركزية حول مرضى انيميا البحر المتوسط فى األطفال و البالغين ومدى االلتزام بالقواعد االرشادية المتعارف عليها والعقبات العملية التى تواجههم
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 2022.
300 ## - PHYSICAL DESCRIPTION
Extent 157 p. :
Other physical details illustrations ;
Dimensions 25cm+
Accompanying material CD
336 ## - CONTENT TYPE
Source rda content
Content type term text
337 ## - MEDIA TYPE
Source rdamedia
Media type term Unmediated
338 ## - CARRIER TYPE
Source rdacarrier
Carrier type term volume
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.)-Cairo nivsersity,2022.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Bibliography: p. 137-157.
520 #3 - SUMMARY, ETC.
Summary, etc. Thalassemia refers to a group of inherited hemoglobinopathies where there<br/>is a quantitative defect in the production of alpha globin or beta globin chains resulting in<br/>precipitation of the unpaired chains, which in turn causes destruction of red blood cell<br/>precursors in the bone marrow (ineffective erythropoiesis) and circulation (hemolysis). It<br/>often requires regular blood transfusions, iron chelation therapy and sometimes<br/>splenectomy for its management. Thus, the therapeutic regime is complex, lifelong and<br/>inconvenient, requiring repeated hospitalizations and blood transfusions, which often<br/>affects the child’s physical and mental health negatively. Treatment adherence is crucial to<br/>Thalassemia control, complications prevention.<br/>Objectives: To evaluate thalassemia major and intermedia management practice and<br/>rate of adherence to guideline at Pediatric Hematology Clinic and Unit, Cairo<br/>University Hospitals, and to analyze the causes of non-adherence to guidelines before<br/>and during the Covid 19 era.<br/>Patients and Methods: This study is a Survey cross-sectional study which was conducted<br/>at the Hematology Clinics in the Children’s Hospitals, Cairo University, in the period from<br/>August 2020 to June 2021, on 100 patients with beta thalassemia major and intermedia<br/>diagnosed and followed-up. Patients were randomly distributed to the physicians and<br/>usually visit the clinic without arranging appointments. On the clinic day, all consecutive<br/>patients and care givers were asked to participate in the study
520 #3 - SUMMARY, ETC.
Summary, etc. يشير مرض انيميا البحر المتوسط إلى مجموعة من اعتالالت الهيموغلوبين المورو ثة حيث يوجد خلل كمي في إنتاج سالسل ألفا هيموجلوبين أو بيتا هيموجلوبين مما يؤدي إلى ترسب السالسل غير المزدوجة، مما يؤدي بدوره إلى تدمير سالئف خاليا الدم الحمراء في نخاع العظام )تكوين غير فعال لكرات الدم الحمراء( والدورة الدموية )تكسير الدم(. نتيجة لذلك، يعاني األفراد المصابون من درجات متفاوتة من االنيميا التكسيرية وتكوين كريات الدم الحمراء خارج النخاع، والذي بدوره يمكن أن يسبب تغيرات في العظام وضعف النمو وزيادة الحديد ا ً ً غالب ما يتطلب عمليات نقل دم منتظمة، ا ً وعالج بإزالة الحديد ا وأحيان استئصال الطحال. وبالتالي، فإن النظام العالجي معقد ومستمر وغير مريح، ويتطلب تكرار دخول المستشفى ونقل الدم، األمر الذي ا ً ً غالب ما يؤثر ا سلب على صحة الطفل الجسدية والعقلية. االلتزام بالعالج أمر بالغ األهمية للسيطرة على انيميا البحر المتوسط والوقاية من المضاعفات
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Issues CD Issues also as CD.
546 ## - LANGUAGE NOTE
Text Language Text in English and abstract in Arabic & English.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Thalassemia refers
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Transfusion
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Eman Abdel-Raouf Mohamed abd Elal
Relator term thesis advisor.
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Niveen Mohamed Salama
Relator term thesis advisor.
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Amera Mohammed Hasnoon
Relator term thesis advisor.
900 ## - Thesis Information
Grant date 01-01-2022
Supervisory body Eman Abdel-Raouf Mohamed abd Elal
-- Niveen Mohamed Salama
-- Amera Mohammed Hasnoon.
Universities Cairo University
Faculties Faculty of Medicine
905 ## - Cataloger and Reviser Names
Cataloger Name Shimaa
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Thesis
Source of classification or shelving scheme Dewey Decimal Classification
Holdings
Source of classification or shelving scheme Home library Current library Date acquired Inventory number Full call number Barcode Date last seen Effective from Koha item type
Dewey Decimal Classification المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 11.02.2024 85818 Cai01.11.28.M.Sc.2022.Me.T 01010110085818000 30.10.2023 30.10.2023 Thesis
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