A Prospective Observational Study of Cardiac Safety, Adverse Drug Reactions And Its Management of Adriamycin + Cyclophosphamide Regimen In Breast Cancer Patients

International Journal of Nursing and Health Science
© 2020 by SSRG - IJNHS Journal
Volume 6 Issue 1
Year of Publication : 2020
Authors : Dr. K.Velavan, M.D., RT, G.Saravanan, M.SC, PGDCR, V.Lalitha M.Pharm, Syam Prakash K.R.Pharm D, Maheshwari V Pharm D, Nithin Joseph Pharm D
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Dr. K.Velavan, M.D., RT, G.Saravanan, M.SC, PGDCR, V.Lalitha M.Pharm, Syam Prakash K.R.Pharm D, Maheshwari V Pharm D, Nithin Joseph Pharm D, "A Prospective Observational Study of Cardiac Safety, Adverse Drug Reactions And Its Management of Adriamycin + Cyclophosphamide Regimen In Breast Cancer Patients," SSRG International Journal of Nursing and Health Science, vol. 6,  no. 1, pp. 28-34, 2020. Crossref, https://doi.org/10.14445/24547484/IJNHS-V6I1P104

Abstract:

This study aims to evaluate cardiac safety, adverse drug reactions, and its management of the Adriamycin+Cyclophosphamide regimen in breast cancer patients. 33 female breast cancer patients enrolled in the study and assigned to the treatment with Adriamycin, Cyclophosphamide, followed by monitoring the cardiac safety analysis, A.D.R., and its management assessed. This study observes that the main way to prevent cardiac toxicity is to limit the cumulative dose of drugs that damage the heart, especially the anthracyclines. There is a defined amount of doxorubicin that can be given with a lesser risk of complications. If the total dose of doxorubicin is less than 550mg/m2, there is a 20 % chance of cardiac toxicity. If the full dose of doxorubicin is between 560-1155mg/m2, the risk increases to 30%.

Keywords:

Adriamycin, Doxorubicin, Cyclophosphamide, A.C. regimen, breast cancer

References:

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