Understanding experiences of patients and family caregivers in the Mayo Clinic Care Transitions program: a qualitative study

被引:7
|
作者
Takahashi, Paul Y. [1 ]
Finnie, Dawn M. [2 ]
Quigg, Stephanie M. [1 ]
Borkenhagen, Lynn S. [1 ]
Kumbamu, Ashok [2 ]
Kimeu, Ashley K. [1 ]
Griffin, Joan M. [2 ,3 ]
机构
[1] Mayo Clin, Dept Internal Med, Div Primary Care Internal Med, Rochester, MN USA
[2] Mayo Clin, Robert D & Patricia E Kern Ctr Sci Hlth Care Deli, Rochester, MN USA
[3] Mayo Clin, Dept Hlth Sci Res, Div Hlth Care Policy & Res, Rochester, MN USA
关键词
geriatrics; home care; program evaluation; nurse practitioner; hospitalization; OLDER-ADULTS; HEART-FAILURE; TERM; DISCHARGE; HOME;
D O I
10.2147/CIA.S183893
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background: Care transitions programs are increasingly used to improve care and reduce re-admission of patients after hospitalization. To learn from the experience of patients who have participated in the Mayo Clinic Care Transitions (MCCT) program and to understand the patient experience, we sought perspectives of patients, caregivers, and providers who worked with participants of the MCCT program. Methods: Investigators interviewed 17 patients and nine of their caregivers about their experience with the MCCT program. Eight health care providers described provider experiences with the MCCT program. Data from semistructured interviews were audio recorded, transcribed, and evaluated through content analysis. Inductive coding methods were used to elicit themes about patient experience with the MCCT program. Results: Patients, caregivers, and providers emphasized that the MCCT program prevented hospitalizations and contributed to the health and quality of life of participants. All three stake-holder groups emphasized the value of the home visit and provision of the visit on a patient's "home turf" as central to the program. Patients appreciated speaking to a provider without the stress and exertion of a trip to the clinic. Caregivers appreciated improved communication provided in the home visit and felt that home visits gave them peace of mind. Patients, caregivers, and providers also identified the need for improved phone triage and communication. Conclusion: Patients, caregivers, and providers acknowledged the care transitions problem and emphasized the benefits of seeing patients on their home turf rather than in an office visit. This qualitative study of patient, caregiver, and provider experiences further validates the importance of the MCCT program.
引用
收藏
页码:17 / 25
页数:9
相关论文
共 50 条
  • [1] Understanding experiences of patients in the Mayo Clinic Care Transitions Program: a Qualitative Study
    Takahashi, P.
    Finnie, D.
    Quigg, S.
    Kumbamu, A.
    Borkenhagen, L.
    Kimeu, A.
    Griffin, J.
    [J]. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2016, 64 : S68 - S68
  • [2] Quality of Life in the Mayo Clinic Care Transitions Program, a Survey Study.
    Faucher, J. J.
    Finnie, D. M.
    Wagie, A. E.
    Rosedahl, J. K.
    Takahashi, P. Y.
    [J]. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2015, 63 : S280 - S280
  • [3] Patient quality of life in the Mayo Clinic Care Transitions program: a survey study
    Faucher, Joshua
    Rosedahl, Jordan
    Finnie, Dawn
    Glasgow, Amy
    Takahashi, Paul
    [J]. PATIENT PREFERENCE AND ADHERENCE, 2016, 10 : 1679 - 1685
  • [4] Experiences of Family Caregivers Providing Home Care to Older Patients With Cancer: A Qualitative Study
    Yang, Cheng-Fang
    Tseng, Chien-Ning
    Liao, Yuan-Ju
    Gao, Zi-Xuan
    Chen, Hsiao-Ping
    Chang, Po-Chih
    Lee, Yun-Hsiang
    [J]. JOURNAL OF NURSING RESEARCH, 2023, 31 (06) : E300
  • [5] A Qualitative Study on Cancer Care Burden: Experiences of Iranian Family Caregivers
    Hassankhani, Hadi
    Eghtedar, Samereh
    Rahmani, Azad
    Ebrahimi, Hossein
    Whitehead, Bill
    [J]. HOLISTIC NURSING PRACTICE, 2019, 33 (01) : 17 - 26
  • [6] Cancer care continuity: A qualitative study on the experiences of French healthcare professionals, patients and family caregivers
    Lelorain, Sophie
    Moreaux, Clemence
    Christophe, Veronique
    Weingertner, Francoise
    Bricout, Helene
    [J]. INTERNATIONAL JOURNAL OF CARE COORDINATION, 2019, 22 (02) : 58 - 68
  • [7] Experiences of patients and caregivers with early palliative care: A qualitative study
    Hannon, Breffni
    Swami, Nadia
    Rodin, Gary
    Pope, Ashley
    Zimmermann, Camilla
    [J]. PALLIATIVE MEDICINE, 2017, 31 (01) : 72 - 81
  • [8] Understanding the Experiences of end of Life Care for Patients with Mesothelioma from the Perspective of Bereaved Family Caregivers in the UK: A Qualitative Analysis
    Harrison, Madeleine
    Darlison, Liz
    Gardiner, Clare
    [J]. JOURNAL OF PALLIATIVE CARE, 2022, 37 (02) : 197 - 203
  • [9] The experiences of family caregivers who participated in a family involvement program after cancer surgery: A qualitative study
    Eskes, Anne Maria
    van Ingen, Cornelia Henrica Nina Maria
    Horst, Mariken Engeltje Elisabeth
    Schreuder, Anne Marthe
    Chaboyer, Wendy
    van Dijkum, Els Jacqueline Maria Nieveen
    [J]. EUROPEAN JOURNAL OF ONCOLOGY NURSING, 2020, 49
  • [10] A qualitative study of older adults' and family caregivers' perspectives regarding their preoperative care transitions
    Malley, Ann M.
    Bourbonniere, Mary
    Naylor, Mary
    [J]. JOURNAL OF CLINICAL NURSING, 2018, 27 (15-16) : 2953 - 2962