Literature DB >> 18450884

Challenges associated with prolonged survival of patients with thalassemia: transitioning from childhood to adulthood.

Khaled Musallam1, Maria D Cappellini, Ali Taher.   

Abstract

Thalassemia is a chronic condition that presents a range of clinical and psychosocial challenges. Although recent advances in the treatment of thalassemia can prolong patient life spans, problems may arise when patients are transferred from pediatric health care settings to adult health care settings. These issues and our recommendations for handling them are discussed.

Entities:  

Mesh：

Year:  2008        PMID： 18450884     DOI： 10.1542/peds.2007-1944

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


  10 in total

1.  Factors affecting health-related quality of life in Thai children with thalassemia.

Authors:  Montarat Thavorncharoensap; Kitti Torcharus; Issarang Nuchprayoon; Arthorn Riewpaiboon; Kaemthong Indaratna; Bang-On Ubol
Journal:  BMC Blood Disord       Date:  2010-01-21

Review 2.  Cure for thalassemia major - from allogeneic hematopoietic stem cell transplantation to gene therapy.

Authors:  Alok Srivastava; Ramachandran V Shaji
Journal:  Haematologica       Date:  2016-12-01       Impact factor: 9.941

Review 3.  Iron overload in thalassemia: different organs at different rates.

Authors:  Ali T Taher; Antoine N Saliba
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

4.  Anxiety and depression affects life and sleep quality in adults with beta-thalassemia.

Authors:  Bashir Hajibeigi; Azita Azarkeyvan; Seyed Moayed Alavian; Maryam Moghani Lankarani; Shervin Assari
Journal:  Indian J Hematol Blood Transfus       Date:  2009-07-05       Impact factor: 0.900

Review 5.  Vitamin D and bone health status in beta thalassemia patients-systematic review.

Authors:  P P Manolopoulos; G Lavranos; I Mamais; A Angouridis; K Giannakou; E O Johnson
Journal:  Osteoporos Int       Date:  2021-01-09       Impact factor: 4.507

6.  Associates of poor physical and mental health-related quality of life in beta thalassemia-major/intermedia.

Authors:  Azita Azarkeivan; Bashir Hajibeigi; Seyed Moayed Alavian; Maryam Moghani Lankarani; Shervin Assari
Journal:  J Res Med Sci       Date:  2009-11       Impact factor: 1.852

7.  A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention.

Authors:  Yeşim Aydınok; Yeşim Oymak; Berna Atabay; Gönül Aydoğan; Akif Yeşilipek; Selma Ünal; Yurdanur Kılınç; Banu Oflaz; Mehmet Akın; Canan Vergin; Melike Sezgin Evim; Ümran Çalışkan; Şule Ünal; Ali Bay; Elif Kazancı; Talia İleri; Didem Atay; Türkan Patıroğlu; Selda Kahraman; Murat Söker; Mediha Akcan; Aydan Akdeniz; Mustafa Büyükavcı; Güçhan Alanoğlu; Özcan Bör; Nur Soyer; Nihal Özdemir Karadaş; Ezgi Uysalol; Meral Türker; Arzu Akçay; Süheyla Ocak; Adalet Meral Güneş; Hüseyin Tokgöz; Elif Ünal; Naci Tiftik; Zeynep Karakaş
Journal:  Turk J Haematol       Date:  2017-04-13       Impact factor: 1.831

8.  Effect of drug use calendar on adherence to iron chelation therapy in young thalassemia patients.

Authors:  Sriwatree Chawsamtong; Arunee Jetsrisuparb; Kirati Kengkla; Siriluk Jaisue
Journal:  Pharm Pract (Granada)       Date:  2022-02-11

9.  Changes in the quality of life of people with thalassemia major between 2001 and 2009.

Authors:  Giorgia Gollo; Gaia Savioli; Manuela Balocco; Cristina Venturino; Elio Boeri; Massimo Costantini; Gian Luca Forni
Journal:  Patient Prefer Adherence       Date:  2013-03-20       Impact factor: 2.711

Review 10.  Novel genetic therapeutic approaches for modulating the severity of β-thalassemia (Review).

Authors:  Fareeha Amjad; Tamseel Fatima; Tuba Fayyaz; Muhammad Aslam Khan; Muhammad Imran Qadeer
Journal:  Biomed Rep       Date:  2020-09-02
  10 in total

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