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. 2021 Apr 26;11(1):8913.
doi: 10.1038/s41598-021-88398-y.

Drug-utilisation profiles and COVID-19

Affiliations

Drug-utilisation profiles and COVID-19

Valentina Orlando et al. Sci Rep. .

Abstract

Coronavirus disease 2019 (COVID-19) has substantially challenged healthcare systems worldwide. By investigating population characteristics and prescribing profiles, it is possible to generate hypotheses about the associations between specific drug-utilisation profiles and susceptibility to COVID-19 infection. A retrospective drug-utilisation study was carried out using routinely collected information from a healthcare database in Campania (Southern Italy). We aimed to discover the prevalence of drug utilisation (monotherapy and polytherapy) in COVID-19 versus non-COVID-19 patients in Campania (~ 6 million inhabitants). The study cohort comprised 1532 individuals who tested positive for COVID-19. Drugs were grouped according to the Anatomical Therapeutic Chemical (ATC) classification system. We noted higher prevalence rates of the use of drugs in the ATC categories C01, B01 and M04, which was probably linked to related comorbidities (i.e., cardiovascular and metabolic). Nevertheless, the prevalence of the use of drugs acting on the renin-angiotensin system, such as antihypertensive drugs, was not higher in COVID-19 patients than in non-COVID-19 patients after adjustments for age and sex. These results highlight the need for further case-control studies to define the effects of medications and comorbidities on susceptibility to and associated mortality from COVID-19.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Differences in prevalence of drug use between the C19G and GPG according to Therapeutic Group (ATC II). C19G COVID-19 group; GPG general population group.
Figure 2
Figure 2
Prevalence of drug use between the C19G and GPG stratified by age group. C19G COVID-19 group; GPG general population group
Figure 3
Figure 3
Chemical Subgroup of the C19G with the highest adjusted relative differences in prevalence stratified by age group. (A) Patients aged 0–39 years. (B) Patients aged 40–59 years. (C) Patients aged 60–79 years. (D) Patients aged > 80.

References

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