PMID- 36588575 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230103 IS - 2297-055X (Print) IS - 2297-055X (Electronic) IS - 2297-055X (Linking) VI - 9 DP - 2022 TI - Effect of arotinolol on chronic heart failure: A systematic review and meta-analysis of randomized controlled trials. PG - 1071387 LID - 10.3389/fcvm.2022.1071387 [doi] LID - 1071387 AB - BACKGROUND: Heart failure is the end stage of all cardiovascular diseases, which brings a heavy burden to the global health network. Arotinolol, as a new type of beta Receptor blocker, has a good antihypertensive effect. Many clinical trials have observed the clinical efficacy of arotinolol in the treatment of essential hypertension. However, so far, there has been no systematic evaluation on the efficacy and safety of arotinolol in the treatment of chronic heart failure. OBJECTIVE: The purpose of this review was to systematically evaluate the clinical efficacy of arotinolol in patients with chronic heart failure. METHODS: Randomized controlled trials (RCTs) of arotinolol in the treatment of chronic heart failure were retrieved from seven databases according to the Cochrane manual, including CNKI (China National Knowledge Infrastructure), Wan fang database, VIP database, PubMed, Sinomed, EMBASE, and the Cochrane Library databases. The main outcomes were the effective rate, left ventricular ejection fraction (LVEF), blood pressure, heart rate, cardiac index, stroke volume (SV), brain natriuretic peptide (BNP), hypersensitive C-reactive protein (Hs-CRP), left ventricular end diastolic volume (LVEDV), left ventricular end diastolic diameter (LVEDD), and adverse events (AEs). RESULTS: A total of 17 trials met the qualification criteria, which included 1,717 patients with heart failure. Most trials had uncertain risks in terms of random sequence generation, allocation hiding, patient loss, and result evaluation. Meta analysis showed that arotinolol significantly improved the treatment efficiency of patients with heart failure (standardized mean difference (SMD) = 4.07, 95% confidence interval (CI) [2.89, 5.72], p = 0.00, I (2) = 0), LVEF (SMD = 1.59, 95% CI [0.99, 2.19], p = 0.000 0, I (2) = 95.8%), cardiac index (SMD = 0.32, 95% CI [0.11, 0.53], p = 0.03), I (2) = 0), SV (SMD = 2.00, 95% CI [1.57, 2.34], p = 0.000, I (2) = 64.2%), lower BNP (SMD = -0.804, 95% CI [-0.97, -0.64], p = 0.000, I (2) = 94.4%), and LVEDV (SMD = -0.25, 95% CI [-0.45, -0.05], p = 0.015, I (2) = 0). There was no statistical significance for blood pressure (SMD(systolic pressure) = -0.09, 95% CI [-0.69, 0.51], p = 0.775, I (2) (systolic pressure) = 90.2%; SMD(diastolic pressure) = -0.16, 95% CI [-0.79, 0.48], P = 0.632, I (2) (diastolic pressure) = 91.2%), heart rate (SMD = -0.12, 95% CI [-1.00, 0.75], P = 0.787, I (2) = 96.1%), Hs-CRP (SMD = -1.52, 95% CI [-3.43, 0.40], P = 0.121, I (2) = 98.3%), and LVEDD (SMD = -0.07, 95% CI [-0.90, 0.76], P = 0.870, I (2) = 96.5%). CONCLUSION: Arotinolol can safely and effectively improve the effective rate of patients with chronic heart failure, increase LVEF, increase CI and SV, and reduce BNP and LVEDV. However, because of the low overall quality of the included randomized controlled trials, these findings need to be considered carefully. More high-quality randomized controlled trials are needed for further verification, to provide a more scientific basis for the safety and effectiveness of arotinolol in the clinical treatment of heart failure. SYSTEMATIC REVIEW REGISTRATION: [https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=371214], identifier [CRD:420223371214]. CI - Copyright (c) 2022 Huang, Song, Wang, Wang, Guo, Zhang, Zhang and Ma. FAU - Huang, Pingping AU - Huang P AD - Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China. AD - Graduate School, China Academy of Chinese Medical Sciences, Beijing, China. FAU - Song, Qingya AU - Song Q AD - Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China. AD - Graduate School, China Academy of Chinese Medical Sciences, Beijing, China. FAU - Wang, Yifei AU - Wang Y AD - Graduate School, China Academy of Chinese Medical Sciences, Beijing, China. AD - Xiyuan Hospital, Beijing University of Chinese Medicine, Beijing, China. FAU - Wang, Anzhu AU - Wang A AD - Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China. AD - Graduate School, China Academy of Chinese Medical Sciences, Beijing, China. FAU - Guo, Lijun AU - Guo L AD - National Clinical Research Center for Chinese Medicine Cardiology, Beijing, China. FAU - Zhang, Hongwei AU - Zhang H AD - Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China. AD - Graduate School, China Academy of Chinese Medical Sciences, Beijing, China. FAU - Zhang, Zhibo AU - Zhang Z AD - Graduate School, China Academy of Chinese Medical Sciences, Beijing, China. AD - Xiyuan Hospital, Beijing University of Chinese Medicine, Beijing, China. FAU - Ma, Xiaochang AU - Ma X AD - National Clinical Research Center for Chinese Medicine Cardiology, Beijing, China. LA - eng PT - Systematic Review DEP - 20221214 PL - Switzerland TA - Front Cardiovasc Med JT - Frontiers in cardiovascular medicine JID - 101653388 PMC - PMC9795060 OTO - NOTNLM OT - arotinolol OT - cardiac insufficiency OT - heart failure OT - meta-analysis OT - randomized controlled trial OT - systematic evaluation COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2023/01/03 06:00 MHDA- 2023/01/03 06:01 PMCR- 2022/01/01 CRDT- 2023/01/02 03:36 PHST- 2022/10/16 00:00 [received] PHST- 2022/11/22 00:00 [accepted] PHST- 2023/01/02 03:36 [entrez] PHST- 2023/01/03 06:00 [pubmed] PHST- 2023/01/03 06:01 [medline] PHST- 2022/01/01 00:00 [pmc-release] AID - 10.3389/fcvm.2022.1071387 [doi] PST - epublish SO - Front Cardiovasc Med. 2022 Dec 14;9:1071387. doi: 10.3389/fcvm.2022.1071387. eCollection 2022.