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Pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy

BACKGROUND: Drug therapy today is remarkably safe and efficacious. Still, some drugs - particularly anticancer drugs - are fraught with numerous adverse drug reactions (ADRs), severely jeopardizing quality of life of cancer patients. Fortunately, most of these ADRs are preventable provided adequate...

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Autores principales: Singh, Shruti, Singh, Prashant Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799948/
https://www.ncbi.nlm.nih.gov/pubmed/29430414
http://dx.doi.org/10.4103/picr.PICR_156_16
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author Singh, Shruti
Singh, Prashant Kumar
author_facet Singh, Shruti
Singh, Prashant Kumar
author_sort Singh, Shruti
collection PubMed
description BACKGROUND: Drug therapy today is remarkably safe and efficacious. Still, some drugs - particularly anticancer drugs - are fraught with numerous adverse drug reactions (ADRs), severely jeopardizing quality of life of cancer patients. Fortunately, most of these ADRs are preventable provided adequate prophylactic drugs are administered along with chemotherapy. AIMS: The aim of this study is to assess the pattern and impact of cytoprotective prophylactic drugs on anticancer ADRs in patients receiving cancer chemotherapy. SUBJECTS AND METHODS: We included 200 patients receiving anticancer therapy for the first time. Patient details and for each cycle: details of baseline investigations, anticancer treatment given, ADRs observed and interventions done to prevent and manage the ADRs were recorded. Preventability and predictability scales were applied to assess the impact of drugs and strategies toward toxicity amelioration. Data were analyzed using descriptive statistics. RESULTS: Adjuvant drugs were administered prophylactically along with anticancer drugs for the prevention of nausea and vomiting, gastritis, immediate allergic reactions, nephrotoxicity, ototoxicity, hemorrhagic cystitis, and other anticipated ADRs. About 94.80% reactions were found to be predictable and 5.20% unpredictable. Maximum reactions (56.47%) were probably preventable. Paracetamol, filgrastim, mucaine, etc., were used to manage a variety of ADRs. CONCLUSIONS: Although the predictability of ADRs was almost 95%, we could prevent only about 56% of them. Surprisingly, we have no ADRs that appear definitely preventable. This could be due to less attention being paid to the ADRs that could have been prevented by the appropriate use of prophylactic measures.
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spelling pubmed-57999482018-02-09 Pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy Singh, Shruti Singh, Prashant Kumar Perspect Clin Res Original Article BACKGROUND: Drug therapy today is remarkably safe and efficacious. Still, some drugs - particularly anticancer drugs - are fraught with numerous adverse drug reactions (ADRs), severely jeopardizing quality of life of cancer patients. Fortunately, most of these ADRs are preventable provided adequate prophylactic drugs are administered along with chemotherapy. AIMS: The aim of this study is to assess the pattern and impact of cytoprotective prophylactic drugs on anticancer ADRs in patients receiving cancer chemotherapy. SUBJECTS AND METHODS: We included 200 patients receiving anticancer therapy for the first time. Patient details and for each cycle: details of baseline investigations, anticancer treatment given, ADRs observed and interventions done to prevent and manage the ADRs were recorded. Preventability and predictability scales were applied to assess the impact of drugs and strategies toward toxicity amelioration. Data were analyzed using descriptive statistics. RESULTS: Adjuvant drugs were administered prophylactically along with anticancer drugs for the prevention of nausea and vomiting, gastritis, immediate allergic reactions, nephrotoxicity, ototoxicity, hemorrhagic cystitis, and other anticipated ADRs. About 94.80% reactions were found to be predictable and 5.20% unpredictable. Maximum reactions (56.47%) were probably preventable. Paracetamol, filgrastim, mucaine, etc., were used to manage a variety of ADRs. CONCLUSIONS: Although the predictability of ADRs was almost 95%, we could prevent only about 56% of them. Surprisingly, we have no ADRs that appear definitely preventable. This could be due to less attention being paid to the ADRs that could have been prevented by the appropriate use of prophylactic measures. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5799948/ /pubmed/29430414 http://dx.doi.org/10.4103/picr.PICR_156_16 Text en Copyright: © 2018 Perspectives in Clinical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Singh, Shruti
Singh, Prashant Kumar
Pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy
title Pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy
title_full Pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy
title_fullStr Pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy
title_full_unstemmed Pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy
title_short Pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy
title_sort pattern and impact of drugs targeted toward toxicity amelioration in patients receiving cancer chemotherapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799948/
https://www.ncbi.nlm.nih.gov/pubmed/29430414
http://dx.doi.org/10.4103/picr.PICR_156_16
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