Literature DB >> 29624126

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

Agatha M Gallo1, Crystal Patil1, Tokunbo Adeniyi1, Lewis L Hsu1, Damiano Rondelli1, Santosh Saraf1.   

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) from a human leukocyte antigen (HLA)-matched sibling donor offers a unique therapy to reverse SCD. This mixed-methods study explores recipients' perception of HSCT success, personal life goals, and associated health-related quality of life (HRQOL) more than 1 year after HSCT. Recipients completed the Short Form-36, version 1 (SF-36v1) HRQOL survey followed by a 60- to 90-min face-to-face or telephone audio-recorded interview. Eleven of 15 eligible recipients participated in the study. Although the eight HRQOL subscale scores varied, the three recipients with a successful HSCT and the highest scores were pursuing their personal life goals. The four with avascular necrosis (AVN) had lower scores related to AVN limitations, yet they were pursuing their personal goals. The two reporting a failed HSCT had reverted back to having SCD, and their subscale scores were among the lowest. Our results show that HSCT success, ability to pursue goals, and HRQOL align in predictable ways.

Entities:  

Keywords:  health-related quality of life; mixed methods; personal life goals; sickle cell disease; stem cell transplantation

Mesh:

Year:  2018        PMID: 29624126      PMCID: PMC6167199          DOI: 10.1177/0193945918768277

Source DB:  PubMed          Journal:  West J Nurs Res        ISSN: 0193-9459            Impact factor:   1.967


  46 in total

Review 1.  Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years.

Authors:  Shruti Chaturvedi; Michael R DeBaun
Journal:  Am J Hematol       Date:  2016-01       Impact factor: 10.047

Review 2.  Sickle Cell Disease.

Authors:  Frédéric B Piel; Martin H Steinberg; David C Rees
Journal:  N Engl J Med       Date:  2017-04-20       Impact factor: 91.245

Review 3.  Sickle Cell Disease: A Brief Update.

Authors:  Sharl Azar; Trisha E Wong
Journal:  Med Clin North Am       Date:  2016-12-14       Impact factor: 5.456

4.  Fatigue in Children With Sickle Cell Disease: Association With Neurocognitive and Social-Emotional Functioning and Quality of Life.

Authors:  Lindsay M Anderson; Taryn M Allen; Courtney D Thornburg; Melanie J Bonner
Journal:  J Pediatr Hematol Oncol       Date:  2015-11       Impact factor: 1.289

Review 5.  Health-related quality of life in patients with hemoglobinopathies.

Authors:  Julie A Panepinto
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2012

6.  Health-related quality of life after allogeneic hematopoietic stem cell transplantation for sickle cell disease.

Authors:  Monica Bhatia; Elissa Kolva; Laura Cimini; Zhezhen Jin; Prakash Satwani; Mirko Savone; Diane George; James Garvin; Mary Llenell Paz; Courtney Briamonte; Eduvigis Cruz-Arrieta; Stephen Sands
Journal:  Biol Blood Marrow Transplant       Date:  2015-01-02       Impact factor: 5.742

7.  The MOS 36-item Short-Form Health Survey (SF-36): III. Tests of data quality, scaling assumptions, and reliability across diverse patient groups.

Authors:  C A McHorney; J E Ware; J F Lu; C D Sherbourne
Journal:  Med Care       Date:  1994-01       Impact factor: 2.983

8.  Financial Hardship and Patient-Reported Outcomes after Hematopoietic Cell Transplantation.

Authors:  Gregory A Abel; Randy Albelda; Nandita Khera; Theresa Hahn; Diana Y Salas Coronado; Oreofe O Odejide; Kira Bona; Reginald Tucker-Seeley; Robert Soiffer
Journal:  Biol Blood Marrow Transplant       Date:  2016-05-13       Impact factor: 5.742

Review 9.  Hematopoietic stem cell transplantation for sickle cell disease: state of the science.

Authors:  Julie-An Talano; Mitchell S Cairo
Journal:  Eur J Haematol       Date:  2014-10-10       Impact factor: 2.997

10.  "Cure" for multiple sclerosis (MS)-Evolving views of therapy goals in patients on different stages of the disease: A pilot study in a cohort of Polish MS patients.

Authors:  Weronika Chacińska; Marta Brzostowska; Monika Nojszewska; Aleksandra Podlecka-Piętowska; Wiesław W Jędrzejczak; Emilian Snarski
Journal:  Brain Behav       Date:  2017-05-02       Impact factor: 2.708

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  2 in total

1.  A systematic review of quality of life in sickle cell disease and thalassemia after stem cell transplant or gene therapy.

Authors:  Sherif M Badawy; Usman Beg; Robert I Liem; Sonali Chaudhury; Alexis A Thompson
Journal:  Blood Adv       Date:  2021-01-26

Review 2.  Evidence-Based Minireview: In young children with severe sickle cell disease, do the benefits of HLA-identical sibling donor HCT outweigh the risks?

Authors:  Niketa Shah; Lakshmanan Krishnamurti
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2021-12-10
  2 in total

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