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Evaluation of potential drug-drug interactions and polypharmacy in hospitalized COVID-19 patients

BACKGROUND: Drugs that are used in COVID-19 infection, may interact with each other, as well as with the drugs for comorbidities, used concomitantly with COVID-19 treatment. OBJECTIVES: It is quite important to calculate and present the patients' exposure to clinically important potential drug-...

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Autores principales: Kilit, Türkan Paşalı, Özyiğit, Filiz, Erarslan, Sertaş, Onbaşı, Kevser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Makerere Medical School 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10117511/
https://www.ncbi.nlm.nih.gov/pubmed/37092113
http://dx.doi.org/10.4314/ahs.v22i4.65
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author Kilit, Türkan Paşalı
Özyiğit, Filiz
Erarslan, Sertaş
Onbaşı, Kevser
author_facet Kilit, Türkan Paşalı
Özyiğit, Filiz
Erarslan, Sertaş
Onbaşı, Kevser
author_sort Kilit, Türkan Paşalı
collection PubMed
description BACKGROUND: Drugs that are used in COVID-19 infection, may interact with each other, as well as with the drugs for comorbidities, used concomitantly with COVID-19 treatment. OBJECTIVES: It is quite important to calculate and present the patients' exposure to clinically important potential drug-drug interactions (pDDIs). We aimed to investigate the pDDIs and the burden of polypharmacy in COVID-19. METHODS: The medical records of 126 consecutive inpatients with COVID-19 treatment were retrospectively analyzed. The Lexi-interact database was used to investigate pDDIs. RESULTS: According to the Lexi-interact database, 605 pDDIs were detected. Of these pDDIs, 23 (3.8%) were A risk category interaction, 186 (30.7%) were B risk category interaction, 339 (56%) were C risk category interaction, 54 (8.9%) were D risk category interaction, and 3 (0.5%) were X risk category interaction. Sixty-five-point five percent of pDDIs (n=396) were clinically important pDDIs (C, D, and X categories), and 69 patients (54.8%) had at least one clinically important pDDIs. The most interacting drug was hydroxychloroquine (n=171, 28.3%). Hydroxychloroquine was also the most interacting drug in the C risk category (n=101, 29.8%) and had 19 pDDIs with metformin, 16 pDDIs with beta-blockers, 13 pDDIs with acetylsalicylic acid, and 10 pDDIs with insulin in the C risk category. Enoxaparin was the most interacting drug (n=25, 46.3%) in the D risk category and most of them were with acetylsalicylic acid (n=12). The most common possible clinical manifestations of pDDIs were QT prolongation, hypoglycemia, and hemorrhage. One hundred and eighteen patients (93.6%) used five or more drugs daily. There was a significant positive correlation between the number of drugs prescribed to patients and the number of clinically important pDDIs (r=0.80, p<0.001). CONCLUSIONS: Clinically important pDDIs are common among COVID-19 patients and the majority of pDDIs require monitoring of therapy. COVID-19 patients should be closely observed for QT prolongation, hypoglycemia, and hemorrhage due to pDDIs during treatment.
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spelling pubmed-101175112023-04-21 Evaluation of potential drug-drug interactions and polypharmacy in hospitalized COVID-19 patients Kilit, Türkan Paşalı Özyiğit, Filiz Erarslan, Sertaş Onbaşı, Kevser Afr Health Sci Articles BACKGROUND: Drugs that are used in COVID-19 infection, may interact with each other, as well as with the drugs for comorbidities, used concomitantly with COVID-19 treatment. OBJECTIVES: It is quite important to calculate and present the patients' exposure to clinically important potential drug-drug interactions (pDDIs). We aimed to investigate the pDDIs and the burden of polypharmacy in COVID-19. METHODS: The medical records of 126 consecutive inpatients with COVID-19 treatment were retrospectively analyzed. The Lexi-interact database was used to investigate pDDIs. RESULTS: According to the Lexi-interact database, 605 pDDIs were detected. Of these pDDIs, 23 (3.8%) were A risk category interaction, 186 (30.7%) were B risk category interaction, 339 (56%) were C risk category interaction, 54 (8.9%) were D risk category interaction, and 3 (0.5%) were X risk category interaction. Sixty-five-point five percent of pDDIs (n=396) were clinically important pDDIs (C, D, and X categories), and 69 patients (54.8%) had at least one clinically important pDDIs. The most interacting drug was hydroxychloroquine (n=171, 28.3%). Hydroxychloroquine was also the most interacting drug in the C risk category (n=101, 29.8%) and had 19 pDDIs with metformin, 16 pDDIs with beta-blockers, 13 pDDIs with acetylsalicylic acid, and 10 pDDIs with insulin in the C risk category. Enoxaparin was the most interacting drug (n=25, 46.3%) in the D risk category and most of them were with acetylsalicylic acid (n=12). The most common possible clinical manifestations of pDDIs were QT prolongation, hypoglycemia, and hemorrhage. One hundred and eighteen patients (93.6%) used five or more drugs daily. There was a significant positive correlation between the number of drugs prescribed to patients and the number of clinically important pDDIs (r=0.80, p<0.001). CONCLUSIONS: Clinically important pDDIs are common among COVID-19 patients and the majority of pDDIs require monitoring of therapy. COVID-19 patients should be closely observed for QT prolongation, hypoglycemia, and hemorrhage due to pDDIs during treatment. Makerere Medical School 2022-12 /pmc/articles/PMC10117511/ /pubmed/37092113 http://dx.doi.org/10.4314/ahs.v22i4.65 Text en © 2022 Kilit TP et al. https://creativecommons.org/licenses/by/4.0/Licensee African Health Sciences. This is an Open Access article distributed under the terms of the Creative commons Attribution License (https://creativecommons.org/licenses/BY/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Kilit, Türkan Paşalı
Özyiğit, Filiz
Erarslan, Sertaş
Onbaşı, Kevser
Evaluation of potential drug-drug interactions and polypharmacy in hospitalized COVID-19 patients
title Evaluation of potential drug-drug interactions and polypharmacy in hospitalized COVID-19 patients
title_full Evaluation of potential drug-drug interactions and polypharmacy in hospitalized COVID-19 patients
title_fullStr Evaluation of potential drug-drug interactions and polypharmacy in hospitalized COVID-19 patients
title_full_unstemmed Evaluation of potential drug-drug interactions and polypharmacy in hospitalized COVID-19 patients
title_short Evaluation of potential drug-drug interactions and polypharmacy in hospitalized COVID-19 patients
title_sort evaluation of potential drug-drug interactions and polypharmacy in hospitalized covid-19 patients
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10117511/
https://www.ncbi.nlm.nih.gov/pubmed/37092113
http://dx.doi.org/10.4314/ahs.v22i4.65
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