PMID- 36286821 OWN - NLM STAT- MEDLINE DCOM- 20221028 LR - 20221207 IS - 0040-3660 (Print) IS - 0040-3660 (Linking) VI - 93 IP - 10 DP - 2021 Oct 15 TI - [Retrospective analysis of clinical outcomes of patients with COVID-19 depending on receiving antihypertensive, lipid-lowering and antihypertensive therapy]. PG - 1193-1202 LID - 10.26442/00403660.2021.10.201072 [doi] AB - BACKGROUND: The main factors that increase the risk of cardiovascular accidents and mortality among patients with COVID-19 include hyperglycemia, arterial hypertension and dyslipidemia. Therefore, all patients with COVID-19 and metabolic syndrome should receive antihypertensive (AHT), hypolipidemic (GLT) and hypoglycemic therapy (GGT). Currently, there is a limited number of studies regarding the effectiveness and safety of this therapy in patients with COVID-19. AIM: Evaluate the clinical outcomes of patients with COVID-19, depending on the recipient of AHT, GLT and GGT. MATERIALS AND METHODS: A retrospective analysis of the clinical outcomes "discharged/died" of 1753 patients with COVID-19 was carried out depending on the received AHT, GLT and GGT. RESULTS: A significant reduction in the risk of mortality among patients with COVID-19 was observed during therapy with angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers ACE inhibitors/ARBs (OR 0.39, 95% CI 0.210.72; p0.05) and b-adrenergic blockers b-AB (OR 0.53, 95% CI 0.281; p0.05). At the same time, against the background of therapy with ACE inhibitors/ARBs and b-ABs, the chance of mortality decreased more significantly among patients with type 2 diabetes mellitus (T2DM) compared with patients without T2DM. Diuretic therapy was associated with a 3-fold increase in the chances of death: OR 3.33, 95% CI 1.884.79; p0.05. Statin therapy did not affect clinical outcomes in COVID-19 patients. On the background of therapy with oral hypoglycemic drugs, the risk of mortality decreased 5-fold (OR 0.19, 95% CI 0.070.54; p0.05). Against the background of insulin therapy, there was an increase in mortality risk by 2.8 times (OR 2.81, 95% CI 1.55.29; p0.05). CONCLUSION: A significant reduction in mortality among patients with COVID-19 was observed during therapy with ACEI/ARB, b-AB, and oral hypoglycemic therapy. Increased risk of death was associated with insulin therapy and diuretic therapy. FAU - Demidova, T Y AU - Demidova TY AUID- ORCID: 0000-0001-6385-540X AD - Pirogov Russian National Research Medical University. FAU - Lobanova, K G AU - Lobanova KG AUID- ORCID: 0000-0002-3656-0312 AD - Pirogov Russian National Research Medical University. FAU - Perekhodov, S N AU - Perekhodov SN AUID- ORCID: 0000-0002-6276-2305 AD - Demikhov Clinical City Hospital. FAU - Antsiferov, M B AU - Antsiferov MB AUID- ORCID: 0000-0002-9944-2997 AD - Endocrinological Dispensary. FAU - Oynotkinova, O S AU - Oynotkinova OS AUID- ORCID: 0000-0002-9856-8643 AD - Pirogov Russian National Research Medical University. LA - rus PT - English Abstract PT - Journal Article DEP - 20211015 PL - Russia (Federation) TA - Ter Arkh JT - Terapevticheskii arkhiv JID - 2984818R RN - 0 (Antihypertensive Agents) RN - 0 (Angiotensin Receptor Antagonists) RN - 0 (Angiotensin-Converting Enzyme Inhibitors) RN - 0 (Hydroxymethylglutaryl-CoA Reductase Inhibitors) RN - 0 (Adrenergic Antagonists) RN - 0 (Hypoglycemic Agents) RN - 0 (Diuretics) RN - 0 (Insulins) RN - 0 (Lipids) SB - IM MH - Humans MH - Antihypertensive Agents/adverse effects MH - Angiotensin Receptor Antagonists/adverse effects MH - Angiotensin-Converting Enzyme Inhibitors/adverse effects MH - Retrospective Studies MH - *Diabetes Mellitus, Type 2/complications MH - *Hydroxymethylglutaryl-CoA Reductase Inhibitors MH - *Hypertension/drug therapy/complications MH - Adrenergic Antagonists/therapeutic use MH - Hypoglycemic Agents/adverse effects MH - Diuretics MH - *Insulins/therapeutic use MH - Lipids MH - *COVID-19 Drug Treatment OTO - NOTNLM OT - COVID-19 OT - antihypertensive drugs OT - favipiravirum OT - hypertension OT - hypoglycemic drugs OT - type 2 diabetes mellitus EDAT- 2022/10/27 06:00 MHDA- 2022/10/29 06:00 CRDT- 2022/10/26 09:54 PHST- 2021/11/04 00:00 [received] PHST- 2021/11/04 00:00 [accepted] PHST- 2022/10/26 09:54 [entrez] PHST- 2022/10/27 06:00 [pubmed] PHST- 2022/10/29 06:00 [medline] AID - 10.26442/00403660.2021.10.201072 [doi] PST - epublish SO - Ter Arkh. 2021 Oct 15;93(10):1193-1202. doi: 10.26442/00403660.2021.10.201072.