A Systematic Review and Metasynthesis of Hematopoietic Stem Cell Transplant (HSCT) Patient's Experiences of Long-Term Monitoring Clinics from the Patient's Perspective

Author:

Bell Blossom1ORCID,Thursby Stacie2,Limbrick Helen3,Swainston Katherine4

Affiliation:

1. Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK

2. Northumbria Healthcare NHS Foundation Trust, North Tyneside General Hospital, Rake Lane, Tyne and Wear, North Shields, UK

3. School of Social Sciences, Humanities & Law, Teesside University, Middlesbrough, Tees Valley, UK

4. School of Psychology, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK

Abstract

This study aimed to synthesize all qualitative evidence on the experiences of hematopoietic stem cell transplant (HSCT) patients attending long-term monitoring clinics from their perspective. A systematic search of the literature was undertaken across 8 databases. The Critical Appraisal Skills Program was used to evaluate each study's quality. Confidence in the Evidence from Reviews of Qualitative Research was employed to assess confidence in each finding. Three themes from 4 qualitative studies were identified relating to patients’ experiences, “[It's] important to maintain a good relationship with the nurses and doctors,” “There's always the thing about the logistics,” and “Once you have cancer, you’re always thinking do I have it again?”. The findings suggest that HSCT patients’ experiences of long-term follow-up care clinics are influenced by the patient-provider relationship and the logistical set-up of monitoring practices, and weakly connected with fear of cancer recurrence. Future research is needed to understand the impact of each finding of this review, specifically in relation to patients’ country of residence to gain a greater understanding of their monitoring support needs.

Publisher

SAGE Publications

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