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Time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis
PURPOSE: Intravenous (IV) zoledronic acid (ZA) is commonly used to delay skeletal complications secondary to bone metastases. However, the time associated with ZA administration may represent a significant burden to healthcare providers and patients. This study assessed the time associated with IV Z...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304336/ https://www.ncbi.nlm.nih.gov/pubmed/22427731 http://dx.doi.org/10.2147/CMAR.S27693 |
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author | Richhariya, Akshara Qian, Yi Zhao, Yufan Chung, Karen |
author_facet | Richhariya, Akshara Qian, Yi Zhao, Yufan Chung, Karen |
author_sort | Richhariya, Akshara |
collection | PubMed |
description | PURPOSE: Intravenous (IV) zoledronic acid (ZA) is commonly used to delay skeletal complications secondary to bone metastases. However, the time associated with ZA administration may represent a significant burden to healthcare providers and patients. This study assessed the time associated with IV ZA infusion in patients with bone metastases secondary to breast or prostate cancer (BC or PC) in the clinic setting. METHODS: Eligible BC or PC patients with bone metastases scheduled to receive IV ZA were observed at seven US-based oncology clinics. Trained observers recorded the time for preinfusion tasks, ZA drug preparation, intravenous infusion, and follow-up activities. RESULTS: Data are reported for 39 patients (BC: 24; PC: 15). Mean administration time was 69 (standard deviation [SD] 42) minutes for all patients combined, 72 (SD 47) minutes for BC, and 65 (SD 33) minutes for PC. Activity times were comparable between tumor types. Mean time for preinfusion tasks (eg, assessment of vital signs, blood draw) and ZA preparation were 12 (SD 20) minutes and 2 (SD 1) minutes, respectively. Mean time required for intravenous infusion (ZA infusion and hydration, when provided) and follow-up activities were 54 (SD 31) minutes and 2 (SD 1) minutes, respectively. CONCLUSION: Infusion time was the greatest time commitment associated with IV ZA administration, representing 78% of the total time on average. Time for preinfusion activities varied substantially. Overall, the mean time for ZA administration represents a notable time burden for healthcare providers and patients. |
format | Online Article Text |
id | pubmed-3304336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33043362012-03-16 Time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis Richhariya, Akshara Qian, Yi Zhao, Yufan Chung, Karen Cancer Manag Res Original Research PURPOSE: Intravenous (IV) zoledronic acid (ZA) is commonly used to delay skeletal complications secondary to bone metastases. However, the time associated with ZA administration may represent a significant burden to healthcare providers and patients. This study assessed the time associated with IV ZA infusion in patients with bone metastases secondary to breast or prostate cancer (BC or PC) in the clinic setting. METHODS: Eligible BC or PC patients with bone metastases scheduled to receive IV ZA were observed at seven US-based oncology clinics. Trained observers recorded the time for preinfusion tasks, ZA drug preparation, intravenous infusion, and follow-up activities. RESULTS: Data are reported for 39 patients (BC: 24; PC: 15). Mean administration time was 69 (standard deviation [SD] 42) minutes for all patients combined, 72 (SD 47) minutes for BC, and 65 (SD 33) minutes for PC. Activity times were comparable between tumor types. Mean time for preinfusion tasks (eg, assessment of vital signs, blood draw) and ZA preparation were 12 (SD 20) minutes and 2 (SD 1) minutes, respectively. Mean time required for intravenous infusion (ZA infusion and hydration, when provided) and follow-up activities were 54 (SD 31) minutes and 2 (SD 1) minutes, respectively. CONCLUSION: Infusion time was the greatest time commitment associated with IV ZA administration, representing 78% of the total time on average. Time for preinfusion activities varied substantially. Overall, the mean time for ZA administration represents a notable time burden for healthcare providers and patients. Dove Medical Press 2012-02-22 /pmc/articles/PMC3304336/ /pubmed/22427731 http://dx.doi.org/10.2147/CMAR.S27693 Text en © 2012 Richhariya et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Richhariya, Akshara Qian, Yi Zhao, Yufan Chung, Karen Time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis |
title | Time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis |
title_full | Time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis |
title_fullStr | Time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis |
title_full_unstemmed | Time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis |
title_short | Time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis |
title_sort | time associated with intravenous zoledronic acid administration in patients with breast or prostate cancer and bone metastasis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304336/ https://www.ncbi.nlm.nih.gov/pubmed/22427731 http://dx.doi.org/10.2147/CMAR.S27693 |
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