Literature DB >> 22522407

Health-related quality of life in sickle cell disease: past, present, and future.

Julie A Panepinto1, Melanie Bonner.   

Abstract

Health-related quality of life (HRQL) is defined as the patient's appraisal of how his/her well being and level of functioning, compared to the perceived ideal, are affected by individual health. The study of HRQL in children and adults with sickle cell disease (SCD) has begun to flourish. Given the devastating complications of the disease and other co-morbid factors patients experience that influence HRQL, it is increasingly important to understand HRQL. The focus of this critical review was to examine past and current research in HRQL in SCD where a validated instrument was used. In addition, future directions for HRQL in SCD are explored.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22522407     DOI: 10.1002/pbc.24176

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  57 in total

1.  Psychosocial burden of sickle cell disease on parents with an affected child in Cameroon.

Authors:  Ambroise Wonkam; Caryl Zameyo Mba; Dora Mbanya; Jeanne Ngogang; Raj Ramesar; Fru F Angwafo
Journal:  J Genet Couns       Date:  2013-07-24       Impact factor: 2.537

2.  Psychometric Properties of the Psychosocial Assessment Tool-General in Adolescents and Young Adults With Sickle Cell Disease.

Authors:  Lori E Crosby; Naomi E Joffe; Nina Reynolds; James L Peugh; Ellen Manegold; Ahna L H Pai
Journal:  J Pediatr Psychol       Date:  2015-08-13

3.  Reproductive health choices for young adults with sickle cell disease or trait: randomized controlled trial immediate posttest effects.

Authors:  Diana J Wilkie; Agatha M Gallo; Yingwei Yao; Robert E Molokie; Christine Stahl; Patricia E Hershberger; Zhongsheng Zhao; Marie L Suarez; Robert J Labotka; Bonnye Johnson; Rigo Angulo; Veronica Angulo; Jesus Carrasco; David Shuey; Stephanie Pelligra; Edward Wang; Dennie T Rogers; Alexis A Thompson
Journal:  Nurs Res       Date:  2013 Sep-Oct       Impact factor: 2.381

4.  Health-Related Quality of Life and Personal Life Goals of Adults With Sickle Cell Disease After Hematopoietic Stem Cell Transplantation.

Authors:  Agatha M Gallo; Crystal Patil; Tokunbo Adeniyi; Lewis L Hsu; Damiano Rondelli; Santosh Saraf
Journal:  West J Nurs Res       Date:  2018-04-06       Impact factor: 1.967

5.  Selection-free genome editing of the sickle mutation in human adult hematopoietic stem/progenitor cells.

Authors:  Mark A DeWitt; Wendy Magis; Nicolas L Bray; Tianjiao Wang; Jennifer R Berman; Fabrizia Urbinati; Seok-Jin Heo; Therese Mitros; Denise P Muñoz; Dario Boffelli; Donald B Kohn; Mark C Walters; Dana Carroll; David I K Martin; Jacob E Corn
Journal:  Sci Transl Med       Date:  2016-10-12       Impact factor: 17.956

6.  Predictors of health-related quality of life over time among adolescents and young adults with sickle cell disease.

Authors:  Jamie L Jackson; Kathleen L Lemanek; Emily Clough-Paabo; Melissa Rhodes
Journal:  J Clin Psychol Med Settings       Date:  2014-12

7.  Ambulatory quality indicators to prevent infection in sickle cell disease.

Authors:  Lauren M Beverung; David Brousseau; Raymond G Hoffmann; Ke Yan; Julie A Panepinto
Journal:  Am J Hematol       Date:  2014-03       Impact factor: 10.047

8.  Psychosocial stressors of sickle cell disease on adult patients in Cameroon.

Authors:  Ambroise Wonkam; Caryl Zameyo Mba; Dora Mbanya; Jeanne Ngogang; Raj Ramesar; Fru F Angwafo
Journal:  J Genet Couns       Date:  2014-02-21       Impact factor: 2.537

9.  Hemoglobin F as a predictor of health-related quality of life in children with sickle cell anemia.

Authors:  Mohamed-Rachid Boulassel; Amira Al-Badi; Mohamed Elshinawy; Juhaina Al-Hinai; Muna Al-Saadoon; Zahra Al-Qarni; Hammad Khan; Rizwan Nabi Qureshi; Yasser Wali
Journal:  Qual Life Res       Date:  2018-10-22       Impact factor: 4.147

10.  Validation of the sickle cell disease pain burden interview-youth.

Authors:  William T Zempsky; Emily A O'Hara; James P Santanelli; Tonya M Palermo; Tamara New; Kim Smith-Whitley; James F Casella
Journal:  J Pain       Date:  2013-05-20       Impact factor: 5.820

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