Practical considerations towards the collection of patient reported outcome data among hematopoietic cell transplant recipients.

ABSTRACT:

Background

There is increasing interest in using patient-reported outcome measures (PROMs) to assess quality of life (QoL) following hematopoietic cell transplant (HCT). However, there is limited consensus on how such data should be collected within HCT services. This survey study investigated health professionals (HCPs) views towards QoL data collection and factors affecting the use of PROMs within HCT centres in the UK.

Method

Individual survey items were based upon the Consolidated Framework for Implementation Research (CFIR). The CFIR consists of five domains which are known to affect intervention (in this instance PROM) adoption and implementation. National coverage was achieved with survey responses received from all UK adult allograft HCT centres.

Results

Findi

SUBMITTER: Pugh G 

PROVIDER: S-EPMC12789203 | biostudies-literature | 2026 Jan

REPOSITORIES: biostudies-literature