2020
DOI: 10.1055/a-1325-0381
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Diabetes Mellitus and Hypertension as Major Risk Factors of Mortality From Covid-19 Pneumonia

Abstract: Hospitalised patients with confirmed COVID-19 pneumonia (n = 172) Patients who died due toCOVID-19 pneumonia (n = 31) Age, years (mean, SD) 61.1 ± 15.8 69.2 ± 13.8 Gender Male (n, %) 98 (57 %) 18 (58 %) Comorbidities (n, %) Hypertension 66 (38.4 %) 24 (77.4 %) Diabetes mellitus 36 (20.9 %) 22 (71 %) Coronary artery disease 18 (10.5 %) 11 (35.5 %) Dyslipidaemia 36 (20.9 %) 16 (51.6 %) Heart failure 21 (12.2 %) 5 (16.1 %) Chronic kidney disease 11 (6.4 %) 3 (9.7 %) 205This document was downloaded for personal us… Show more

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Cited by 16 publications
(14 citation statements)
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“…Hypertension and diabetes mellitus increased susceptibility in SCAP, which they were consistent with our previous finding of SARS-CoV-2 in China [ 41 ] and Petrakisin’s in Greece [ 42 ]. Moreover, 45% of SCAP patients in our cohort were current smokers.…”
Section: Discussionsupporting
confidence: 92%
“…Hypertension and diabetes mellitus increased susceptibility in SCAP, which they were consistent with our previous finding of SARS-CoV-2 in China [ 41 ] and Petrakisin’s in Greece [ 42 ]. Moreover, 45% of SCAP patients in our cohort were current smokers.…”
Section: Discussionsupporting
confidence: 92%
“…Diabetes mellitus (DM) belongs to the comorbidities increasing the risk of severe COVID-19 pneumonia [2]. Notably, in our department among those who died from severe pneumonia, 71 % had DM [3].…”
Section: Dear Editormentioning
confidence: 76%
“…Among the 69 patients with an ordinal score of 6 at baseline, those randomly assigned to the interferon beta-1a plus remdesivir group were more likely to be male (25 [71%] of 35 vs 19 [56%] of 34), present to hospital within 8 days of symptom onset (22 [63%] vs 15 [44%]), be older (median age 58·9 [SD 13·1] years vs 54·7 years [15·0]), have baseline D-dimer concentrations of ≥2·025 mg/L (eight [23%] vs six [18%]), and have baseline C-reactive protein concentrations of ≥100·0 mg/L (21 [60%] vs 16 [47%]) than those in the placebo plus remdesivir group ( appendix pp 26–27, 44, 96 ). Additionally, patients randomly assigned to the interferon beta-1a plus remdesivir group were more likely than those in the placebo plus remdesivir group to have comorbidities shown in other studies to be associated with severe disease: 18 , 19 , 20 type 2 diabetes (19 [54%] vs 11 [32%]), coronary artery disease (20 [60%] vs two [6%]), hypertension 25 [71%] vs 19 [56%]), chronic kidney disease (eight [24%] vs three [9%]), and obesity (21 [60%] vs 22 [65%]; appendix pp 25, 97 ). Univariate and multivariate Cox proportional hazards models were created, adjusting for these baseline characteristics for the primary endpoint, but all models yielded recovery rate ratios consistent with the estimated treatment effect in the primary unadjusted model, indicating worse outcomes with interferon beta-1a in those on high-flow oxygen at baseline ( appendix pp 36–37 ).…”
Section: Resultsmentioning
confidence: 99%