Can you spare 100 days? The allogeneic hematopoietic cell transplant caregiver requirement from the perspective of social workers

被引:1
作者
Preussler, Jaime M. [1 ]
Desalvo, Anna M. [1 ]
Huberty, Paxton [2 ]
Schoeppner, Katie [2 ]
Coles, Jennifer A. Sees [1 ]
机构
[1] NMDP, CIBMTR Ctr Int Blood & Marrow Transplant Res, 500 N 5th St, Minneapolis, MN 55401 USA
[2] NMDP, Minneapolis, MN USA
关键词
Hematopoietic cell transplantation; Caregiver; Social workers; INFORMAL CAREGIVERS; CANCER; BARRIERS; SUPPORT; HEALTH; CARE; QUALITY; ACCESS; THINGS; BLOOD;
D O I
10.1007/s00520-024-08906-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeA caregiver is generally required for a patient to proceed with allogeneic hematopoietic cell transplantation (alloHCT). If continuous caregiver support is not available, alloHCT will likely not be a treatment option. A qualitative study design was used to explore caregiver requirements from the perspectives of social workers (SWs). Secondary objectives included learning about requirement flexibility, barriers, and ideas to support patients and caregivers.MethodsSemi-structured web-based focus groups were conducted with alloHCT SWs who worked with adults at the United States (U.S.) transplant centers (TCs) from May to July 2022. Focus groups explored TC caregiver requirements, including flexibility and exceptions, origins, and barriers.ResultsTwenty-two SWs from TCs across the U.S. participated. All noted their TC required a caregiver to proceed to alloHCT, though there was variation in the length of time a caregiver was required and the distance needed to stay near the TC post-alloHCT. Most participants described differences within the transplant team in allowing exceptions to caregiver requirements. SWs described barriers including finances and patients needing to relocate closer to the TC.ConclusionSWs reported variation in caregiver requirements across TCs. Though variation may allow for some flexibility, it may contribute to access barriers. Additional research is needed to identify essential requirements for safe post-transplant care and monitoring and to develop patient-centered models to help patients access life-saving treatment.
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页数:9
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共 64 条
[1]   The focus groups in social research: advantages and disadvantages [J].
Acocella, Ivana .
QUALITY & QUANTITY, 2012, 46 (04) :1125-1136
[2]   How Caregivers Cope and Adapt When a Family Member Is Diagnosed With a Hematologic Malignancy: Informing Supportive Care Needs [J].
Albrecht, Tara A. ;
Hoppe, Rebecca ;
Winter, Marcia A. .
CANCER NURSING, 2022, 45 (06) :E849-E855
[3]  
American Cancer Society Hope Lodge, What is hope lodge?
[4]  
[Anonymous], Geographic Levels
[5]  
[Anonymous], 2019, Collecting and analyzing qualitative data
[6]  
[Anonymous], 2023, Local Provider Partnership
[7]  
[Anonymous], 2021, NCCN Guidelines Version 1.2022 Non-Small Cell Lung Cancer
[8]   The Effect of Psychosocial Interventions on Outcomes for Caregivers of Hematopoietic Cell Transplant Patients [J].
Bangerter, Lauren R. ;
Griffin, Joan M. ;
Langer, Shelby ;
Hasan, Bashar ;
Kim, Wonsun ;
Murad, M. Hassan ;
Khera, Nandita .
CURRENT HEMATOLOGIC MALIGNANCY REPORTS, 2018, 13 (03) :155-163
[9]   Improved access to HCT with reduced racial disparities through integration with leukemia care and haploidentical donors [J].
Bashey, Asad ;
Zhang, Xu ;
Morris, Lawrence E. ;
Holland, H. K. ;
Bachier-Rodriguez, Lizamarie ;
Solomon, Scott R. ;
Solh, Melhem .
BLOOD ADVANCES, 2023, 7 (15) :3816-3823
[10]  
Bevans Margaret, 2009, Oncol Nurs Forum, V36, pE317, DOI 10.1188/09.ONF.E317-E325