Table 1.
Available evidence summarises hypertension and COVID-19 findings derived from original studies and statements based on the expert opinion following the GRADE rating system.
| Study conclusions | Evidence grade | Ref. |
|---|---|---|
| ACEI/ARBs increase ACE2 receptor expression; SARS-CoV-2 might utilise this increase to result in severe disease | A | [6] |
| Severely ill male patients with heart injury, hyperglycemia, and high-dose corticosteroid use may have a higher risk of death | B | [7] |
| The use of ACEI and/or ARBs can increase the risk of severity of COVID-19 | A | [8] |
| Comorbidities such as COPD, diabetes, hypertension, and malignancy predispose individuals with COVID-19 to adverse clinical outcomes | A | [9] |
| Does not support discontinuation of ACEI/ARB medications that are clinically indicated in the context of the COVID-19 pandemic | B | [10] |
| A significant difference in the use of ACEI/ARB among patients with different severities of the disease | B | [11] |
| ACEI/ARBs reduce IL-6 and increase CD3 and CD8, thus reducing COVID-19 severity; ACEI and ARBs are beneficial in COVID-19 | A | [12] |
| AT1R blockers, including ARBs, can help reduce COVID-19 morbidity and mortality | A | [13] |
| Animal data: increasing ACE2 expression can help protect against pulmonary and cardiovascular hazards; recommend continuing the use of ACEI and ARBs to manage hypertension in COVID-19 patients | A | [14] |
| RAAS inhibitors were shown to be possibly associated with a lower risk of mortality | B | [15] |