Faculty of Medicine, Udayana University, Denpasar, Bali, Indonesia.
Department of Cardiology and Vascular Medicine, Prof. Dr. I.G.N.G Ngoerah General Hospital, Faculty of Medicine, Udayana University, Denpasar, Bali, Indonesia.
Hypertens Res. 2023 Jan;46(1):165-174. doi: 10.1038/s41440-022-01077-x. Epub 2022 Oct 14.
Blood pressure variability (BPV) is essential in hypertensive patients and is frequently associated with organ damage. As of today, hypertension is still the most common comorbidity in COVID-19, but the impact of BPV and the therapeutic target of BPV on outcomes in COVID-19 patients with hypertension remain unclear. Therefore, this study investigated the relationship between BPV and severity of COVID-19, in-hospital mortality, hypertensive status, and efficacy of antihypertensives in suppressing hypertensive covid-19 patient BPV. This cohort retrospective study enrolled 351 patients hospitalized with COVID-19. Subjects were classified according to the severity of COVID-19, the presence of hypertension, and their BPV status. During hospitalization, mean arterial pressure (MAP) was measured at 6 a.m. and 6 p.m., and BPV was calculated as the coefficient of variation of MAP (MAPCV). MAPCV values above the median were defined as high BPV. In addition, we compared the hypertensive status, COVID-19 severity, in-hospital mortality, and antihypertensive agents between the BPV groups. The mean age was 53.85 ± 18.84 years old. Hypertension was significantly associated with high BPV with prevalence ratio (PR) = 1.38 (95% CI = 1.13-1.70; p = 0.003) or severe COVID-19 (PR = 1.39; 95% CI = 1.09-1.76; p = 0.005). In laboratory findings, high BPV group had lower Albumin, higher WBC, serum Cr, CRP, and creatinine to albumin ratio. High BPV status also significantly increased risk of mortality (HR = 2.30; 95% CI = 1.73-3.86; p < 0.001). Patients with a combination of severe COVID-19 status, hypertension, and high BPV status had the highest risk of in-hospital mortality (HR = 3.51; 95% CI = 2.32-4.97; p < 0.001) compared to other combination status groups. In COVID-19 patients with hypertension, combination therapy with calcium channel blockers (CCB) as well as CCB monotherapy significantly develop low BPV (PR = 2.002; 95 CI% = 1.33-3.07; p = 0.004) and low mortality (HR = 0.17; 95% CI = 0.05-0.56; p = 0.004). Hypertensive status and severe COVID-19 were significantly associated with high BPV, and these factors increased in-hospital mortality. CCBs might be antihypertensive agents that potentially effectively suppressing BPV and mortality in COVID-19 patients.
血压变异性(BPV)在高血压患者中很重要,并且经常与器官损伤有关。截至目前,高血压仍然是 COVID-19 最常见的合并症,但 BPV 的影响以及 COVID-19 高血压患者的 BPV 治疗目标对结局的影响仍不清楚。因此,本研究探讨了 BPV 与 COVID-19 严重程度、住院死亡率、高血压状态以及降压药抑制高血压 COVID-19 患者 BPV 的疗效之间的关系。这项队列回顾性研究纳入了 351 名因 COVID-19 住院的患者。根据 COVID-19 的严重程度、高血压的存在以及他们的 BPV 状态对受试者进行分类。住院期间,分别于上午 6 点和下午 6 点测量平均动脉压(MAP),并计算 MAP 的变异系数(MAPCV)作为 BPV。MAPCV 值高于中位数定义为高 BPV。此外,我们比较了 BPV 组之间的高血压状态、COVID-19 严重程度、住院死亡率和降压药。平均年龄为 53.85±18.84 岁。高血压与高 BPV 显著相关,患病率比(PR)为 1.38(95%可信区间,1.13-1.70;p=0.003)或严重 COVID-19(PR)为 1.39(95%可信区间,1.09-1.76;p=0.005)。在实验室发现中,高 BPV 组的白蛋白较低,白细胞计数(WBC)、血清肌酐(Cr)、C 反应蛋白(CRP)和肌酐/白蛋白比值较高。高 BPV 状态也显著增加了死亡率的风险(HR=2.30;95%可信区间,1.73-3.86;p<0.001)。与其他组合状态组相比,同时患有严重 COVID-19 状态、高血压和高 BPV 状态的患者的住院死亡率风险最高(HR=3.51;95%可信区间,2.32-4.97;p<0.001)。在 COVID-19 合并高血压的患者中,钙通道阻滞剂(CCB)联合治疗以及 CCB 单药治疗显著降低了 BPV(PR=2.002;95%置信区间,1.33-3.07;p=0.004)和降低了死亡率(HR=0.17;95%置信区间,0.05-0.56;p=0.004)。高血压状态和严重 COVID-19 与高 BPV 显著相关,这些因素增加了住院死亡率。CCB 可能是一种降压药,能有效抑制 COVID-19 患者的 BPV 和死亡率。