Allograft and patient survival after sequential HSCT and kidney transplantation from the same donor-A multicenter analysis.
Allograft and patient survival after sequential HSCT and kidney transplantation from the same donor-A multicenter analysis.
- Research Article
22
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- Kidney International
Immunosuppressive treatment and progression of histologic lesions in kidney allografts
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121
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- Journal of the American Society of Nephrology
The increased success and availability of transplantation of solid organs other than kidneys has resulted in a large number of patients at risk for the usual medical complications of long-term immunosuppressive therapy. Acute and chronic renal failure play a critical role in the success of these
- Research Article
156
- 10.1053/j.ajkd.2011.04.010
- Jun 16, 2011
- American Journal of Kidney Diseases
Human Cytomegalovirus and Kidney Transplantation: A Clinician's Update
- Supplementary Content
190
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- Jul 1, 2001
- American Journal of Transplantation
Delayed Graft Function: State of the Art, November 10–11, 2000. Summit Meeting, Scottsdale, Arizona, USA
- Research Article
76
- 10.1016/j.bbmt.2010.02.006
- Feb 12, 2010
- Biology of Blood and Marrow Transplantation
Chronic Kidney Disease, Thrombotic Microangiopathy, and Hypertension Following T Cell-Depleted Hematopoietic Stem Cell Transplantation
- Abstract
2
- 10.1182/blood.v110.11.829.829
- Nov 16, 2007
- Blood
Premature Aging of Hematopoietic Cells in Long Term Survivors after HSCT with Chronic GVHD and a Female Donor.
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264
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- Cell Stem Cell
The Promise and Perils of Stem Cell Therapeutics
- Abstract
- 10.1182/blood.v120.21.4350.4350
- Nov 16, 2012
- Blood
T-Cell Depleted Haematopoietic Stem Cells (HSC) Transplantation with Add Back of CD45RA Negative DLI: About 2 Cases
- Abstract
- 10.1182/blood.v118.21.832.832
- Nov 18, 2011
- Blood
Durable Chimerism, Absence of Graft-Versus-Host Disease and the Induction of Donor Specific Tolerance in Recipients of HLA Disparate Living Donor Kidney Transplants and Therapeutic Cell Transfer
- Research Article
17
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- Jan 1, 2011
- Advances in Chronic Kidney Disease
Hypertension Following Kidney Transplantation
- Research Article
209
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- Biology of Blood and Marrow Transplantation
The Incidence of Veno-Occlusive Disease Following Allogeneic Hematopoietic Stem Cell Transplantation Has Diminished and the Outcome Improved over the Last Decade
- Research Article
5
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- Dec 30, 2010
- Biology of Blood and Marrow Transplantation
Translational Research Efforts in Biomarkers and Biology of Early Transplant-Related Complications
- Front Matter
1
- 10.1016/j.gie.2006.04.006
- Sep 1, 2006
- Gastrointestinal Endoscopy
Optimizing care for GI disorders in children after hematopoietic stem cell transplantation
- Discussion
2
- 10.1016/j.bbmt.2014.04.001
- Apr 13, 2014
- Biology of Blood and Marrow Transplantation
Mixed Chimerism: Good News or Bad News?
- Supplementary Content
33
- 10.3389/fpsyg.2017.00253
- Mar 10, 2017
- Frontiers in Psychology
Hematopoietic stem cell transplantation (HSCT) is a standard treatment after disease relapse and failure of conventional treatments for cancer in childhood or as a first line treatment for some high-risk cancers. Since hematopoietic stem cells can be found in the marrow (previously called a bone marrow transplantation) or periphery, we refer to HSCT as inclusive of HSCT regardless of the origin of the stem cells. HSCT is associated with adverse side effects, prolonged hospitalization, and isolation. Previous studies have shown that survivors of HSCT are at particularly high risk for developing late effects and medical complications, and thus, in addition to survival, quality of life in survivors of HSCT is an important outcome. This review summarizes and distills findings on the health-related quality of life (HRQOL) of long-term childhood cancer survivors of HSCT and examines significant sociodemographic, medical, disease and treatment correlates of HRQOL, as well as the methodology of the studies (instruments, type of studies, timing of assessment, type of transplantation). Because previous reviews covered the studies published before 2006, this review searched three databases published between January, 2006, and August, 2016. The search identified nine studies, including 2 prospective cohort studies and 7 cross-sectional studies. All studies reported a follow-up time of >5 years. The review found that HRQOL is significantly impacted over time following childhood HSCT, with salient correlates of HRQOL found to be presence of a severe chronic health or major medical condition, graft vs. host disease (GVHD), or pain. Continual evaluation of HRQOL must be integrated into long-term follow-up after childhood HSCT, and intervention should be offered for those survivors with poor HRQOL. Longitudinal studies should be emphasized in future research to allow for predictor models of resilience and poor HRQOL.