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Impact of Provider Volume on Outcomes of Patients With Hodgkin Lymphoma
BACKGROUND: While the provider volume-outcome relationship has been established for many complex surgeries and invasive procedures, the provider volume impact on outcomes for Hodgkin lymphoma (HL) is less certain. We hypothesized that high-volume providers (HVPs) may have superior outcomes compared...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5942207/ https://www.ncbi.nlm.nih.gov/pubmed/29760832 http://dx.doi.org/10.14740/wjon1093w |
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author | Ireland, Catherine Wiedower, Eric Mirza, Muhammad Crawley, Melissa Tran, Alexandria Yaghmour, George Martin, Mike G. |
author_facet | Ireland, Catherine Wiedower, Eric Mirza, Muhammad Crawley, Melissa Tran, Alexandria Yaghmour, George Martin, Mike G. |
author_sort | Ireland, Catherine |
collection | PubMed |
description | BACKGROUND: While the provider volume-outcome relationship has been established for many complex surgeries and invasive procedures, the provider volume impact on outcomes for Hodgkin lymphoma (HL) is less certain. We hypothesized that high-volume providers (HVPs) may have superior outcomes compared with low-volume providers (LVPs). METHODS: We performed a chart-based, retrospective review of all patients receiving adriamycin, doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) for HL at the West Cancer Center from January 2010 to June 2015. Patients were divided into HVP (> 3 inpatient chemotherapy (CT)/month (m)) versus LVP (< 3 CT per m) groups. Of 95 patients identified, 93 received at least one dose of ABVD, 21 treated by HVP and 72 by LVP. Patient characteristics were well balanced between groups. RESULTS: HVPs were less likely to prescribe dose delays (odds ratio (OR): 0.32; confidence interval (CI): 0.16 - 0.65; P = 0.0007) and to hold doses for afebrile neutropenia (OR: 0.05; CI: 0.00 - 0.85; P = 0.0006). HVP delivered significantly fewer prophylactic growth factors (0% of doses vs. 42%, OR: 0.00; CI < 0.00 - 0.06; P < 0.0001). Both event-free survival (EFS) (HR: 6.68; CI: 1.10 - 7.63; P = 0.0321) and overall survival (OS) (HR: 3.68; CI: 1.11 - 12.22; P = 0.032) were significantly inferior in the patients treated by LVP. CONCLUSIONS: In this study, patients with HL treated by LVP had inferior outcomes compared with those treated by HVP. HVPs were less likely to prescribe dose delays, hold doses for afebrile neutropenia or administer growth factor prophylaxis. These observations need to be confirmed in alternative datasets. |
format | Online Article Text |
id | pubmed-5942207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59422072018-05-14 Impact of Provider Volume on Outcomes of Patients With Hodgkin Lymphoma Ireland, Catherine Wiedower, Eric Mirza, Muhammad Crawley, Melissa Tran, Alexandria Yaghmour, George Martin, Mike G. World J Oncol Original Article BACKGROUND: While the provider volume-outcome relationship has been established for many complex surgeries and invasive procedures, the provider volume impact on outcomes for Hodgkin lymphoma (HL) is less certain. We hypothesized that high-volume providers (HVPs) may have superior outcomes compared with low-volume providers (LVPs). METHODS: We performed a chart-based, retrospective review of all patients receiving adriamycin, doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) for HL at the West Cancer Center from January 2010 to June 2015. Patients were divided into HVP (> 3 inpatient chemotherapy (CT)/month (m)) versus LVP (< 3 CT per m) groups. Of 95 patients identified, 93 received at least one dose of ABVD, 21 treated by HVP and 72 by LVP. Patient characteristics were well balanced between groups. RESULTS: HVPs were less likely to prescribe dose delays (odds ratio (OR): 0.32; confidence interval (CI): 0.16 - 0.65; P = 0.0007) and to hold doses for afebrile neutropenia (OR: 0.05; CI: 0.00 - 0.85; P = 0.0006). HVP delivered significantly fewer prophylactic growth factors (0% of doses vs. 42%, OR: 0.00; CI < 0.00 - 0.06; P < 0.0001). Both event-free survival (EFS) (HR: 6.68; CI: 1.10 - 7.63; P = 0.0321) and overall survival (OS) (HR: 3.68; CI: 1.11 - 12.22; P = 0.032) were significantly inferior in the patients treated by LVP. CONCLUSIONS: In this study, patients with HL treated by LVP had inferior outcomes compared with those treated by HVP. HVPs were less likely to prescribe dose delays, hold doses for afebrile neutropenia or administer growth factor prophylaxis. These observations need to be confirmed in alternative datasets. Elmer Press 2018-04 2018-05-01 /pmc/articles/PMC5942207/ /pubmed/29760832 http://dx.doi.org/10.14740/wjon1093w Text en Copyright 2018, Ireland et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ireland, Catherine Wiedower, Eric Mirza, Muhammad Crawley, Melissa Tran, Alexandria Yaghmour, George Martin, Mike G. Impact of Provider Volume on Outcomes of Patients With Hodgkin Lymphoma |
title | Impact of Provider Volume on Outcomes of Patients With Hodgkin Lymphoma |
title_full | Impact of Provider Volume on Outcomes of Patients With Hodgkin Lymphoma |
title_fullStr | Impact of Provider Volume on Outcomes of Patients With Hodgkin Lymphoma |
title_full_unstemmed | Impact of Provider Volume on Outcomes of Patients With Hodgkin Lymphoma |
title_short | Impact of Provider Volume on Outcomes of Patients With Hodgkin Lymphoma |
title_sort | impact of provider volume on outcomes of patients with hodgkin lymphoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5942207/ https://www.ncbi.nlm.nih.gov/pubmed/29760832 http://dx.doi.org/10.14740/wjon1093w |
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