Cargando…
Improving the turnaround times of infectious disease markers reporting in an NHS stem cell department
The Stem Cell Donation and Transplantation Department at NHS Blood and Transplant (NHSBT) facilitates unrelated donor haematopoietic stem cell transplantations for patients with life-threatening haematological malignancies or other blood diseases. Donors must be screened for infectious disease marke...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196163/ https://www.ncbi.nlm.nih.gov/pubmed/35697357 http://dx.doi.org/10.1136/bmjoq-2022-001814 |
_version_ | 1784727122232737792 |
---|---|
author | Li, Ying Proudlove, Nathan |
author_facet | Li, Ying Proudlove, Nathan |
author_sort | Li, Ying |
collection | PubMed |
description | The Stem Cell Donation and Transplantation Department at NHS Blood and Transplant (NHSBT) facilitates unrelated donor haematopoietic stem cell transplantations for patients with life-threatening haematological malignancies or other blood diseases. Donors must be screened for infectious disease markers (IDMs) prior to donation. The purpose of IDM testing is to assess whether the donor currently has, or previously had, an infectious disease that could be transmitted to the recipient. The turnaround time (TaT) from sample collection to the return of IDM results is important to transplant clinicians and their patients. NHSBT has a target TaT of 80% within seven calendar days. Our initial analysis showed us that we failed to meet this in any week in the previous year, and our service was neither efficient nor consistent, so there was considerable improvement potential. This quality improvement (QI) project aimed to improve the TaT of the IDM reporting service. We tested three change ideas through four Plan-Do-Study-Act (PDSA) cycles. We collected data on TaTs from our laboratory information management system (LIMS) and updated our statistical process control charts after each PDSA cycle. Over the course of the project, we reduced the mean TaT from 8.9 days to 5.5 days and increased the proportion of samples reported within the 7-day benchmark from 50% to 89%, reaching the key performance indicator (KPI) target. Conducting this project was a rewarding experience. Although we encountered unanticipated technical issues during PDSA experiments, and we found that some change plans were not as effective in improving the KPIs as we expected, the improvement by the end of the study period was substantial. This QI project enabled us to meet our TaT targets and, ultimately, help ensure that our patients receive timely transplants. It suggests that QI may have wider applications across our part of NHSBT. |
format | Online Article Text |
id | pubmed-9196163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-91961632022-07-08 Improving the turnaround times of infectious disease markers reporting in an NHS stem cell department Li, Ying Proudlove, Nathan BMJ Open Qual Quality Improvement Programme The Stem Cell Donation and Transplantation Department at NHS Blood and Transplant (NHSBT) facilitates unrelated donor haematopoietic stem cell transplantations for patients with life-threatening haematological malignancies or other blood diseases. Donors must be screened for infectious disease markers (IDMs) prior to donation. The purpose of IDM testing is to assess whether the donor currently has, or previously had, an infectious disease that could be transmitted to the recipient. The turnaround time (TaT) from sample collection to the return of IDM results is important to transplant clinicians and their patients. NHSBT has a target TaT of 80% within seven calendar days. Our initial analysis showed us that we failed to meet this in any week in the previous year, and our service was neither efficient nor consistent, so there was considerable improvement potential. This quality improvement (QI) project aimed to improve the TaT of the IDM reporting service. We tested three change ideas through four Plan-Do-Study-Act (PDSA) cycles. We collected data on TaTs from our laboratory information management system (LIMS) and updated our statistical process control charts after each PDSA cycle. Over the course of the project, we reduced the mean TaT from 8.9 days to 5.5 days and increased the proportion of samples reported within the 7-day benchmark from 50% to 89%, reaching the key performance indicator (KPI) target. Conducting this project was a rewarding experience. Although we encountered unanticipated technical issues during PDSA experiments, and we found that some change plans were not as effective in improving the KPIs as we expected, the improvement by the end of the study period was substantial. This QI project enabled us to meet our TaT targets and, ultimately, help ensure that our patients receive timely transplants. It suggests that QI may have wider applications across our part of NHSBT. BMJ Publishing Group 2022-06-13 /pmc/articles/PMC9196163/ /pubmed/35697357 http://dx.doi.org/10.1136/bmjoq-2022-001814 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Quality Improvement Programme Li, Ying Proudlove, Nathan Improving the turnaround times of infectious disease markers reporting in an NHS stem cell department |
title | Improving the turnaround times of infectious disease markers reporting in an NHS stem cell department |
title_full | Improving the turnaround times of infectious disease markers reporting in an NHS stem cell department |
title_fullStr | Improving the turnaround times of infectious disease markers reporting in an NHS stem cell department |
title_full_unstemmed | Improving the turnaround times of infectious disease markers reporting in an NHS stem cell department |
title_short | Improving the turnaround times of infectious disease markers reporting in an NHS stem cell department |
title_sort | improving the turnaround times of infectious disease markers reporting in an nhs stem cell department |
topic | Quality Improvement Programme |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196163/ https://www.ncbi.nlm.nih.gov/pubmed/35697357 http://dx.doi.org/10.1136/bmjoq-2022-001814 |
work_keys_str_mv | AT liying improvingtheturnaroundtimesofinfectiousdiseasemarkersreportinginannhsstemcelldepartment AT proudlovenathan improvingtheturnaroundtimesofinfectiousdiseasemarkersreportinginannhsstemcelldepartment |