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1.
J Multidiscip Healthc ; 17: 1619-1627, 2024.
Article in English | MEDLINE | ID: mdl-38628615

ABSTRACT

In intensive care units, patients are often restrained to ensure their safety, with physical restraints being the most commonly used method. However, physical restraints compromises the patient's freedom, health and comfort, and nurses often face moral dilemmas when deciding whether to use physical restraints. This article examines physical restraints through the four universal principles of autonomy, beneficence, non-maleficence and justice. Through these principles, the authors will critically explore whether the physical restraints of patients by nurses is ethical in practice and what moral issues exist. This paper also explores conflicts and moral dilemmas for nurses in this context. Finally, suggestions are made on changes to education and clinical practice.

2.
Heliyon ; 9(10): e20594, 2023 Oct.
Article in English | MEDLINE | ID: mdl-37867825

ABSTRACT

Objective: Shenfu Injection (SFI) derived from Shenfu decoction, has been widely used for treating heart failure in China. This meta-analysis aimed to assess the effect of SFI as an adjuvant therapy on quality of life in patients with chronic heart failure (CHF). Methods: A systematic literature search was conducted in CKNI, VIP, Wanfang, Sinomed, Cochrane Library, PubMed, and Embase database until March 16, 2023. Randomized controlled trials (RCTs) evaluating the effect of SFI plus conventional therapy versus conventional therapy alone for treating CHF were included. Outcome measures were quality of life defineded by the Minnesota Living with Heart Failure questionnaire (MLHFQ), left ventricular ejection fraction (LVEF), 6-min walking distance, and blood brain natriuretic peptide (BNP)/N-terminal pro-brain natriuretic peptide (NT-proBNP) level. Results: Thirteen RCTs enrolling 1042 CHF patients were included. SFI plus conventional therapy significantly reduced the total MLHFQ score (mean difference [MD] -8.69 points; 95% confidence intervals [CI] -13.46 to -3.91) compared with the conventional therapy alone. Moreover, adjuvant treatment with SFI significantly improved the 6-min walking distance (MD 65.42 m; 95% CI 44.23 to 86.62), LVEF (MD 3.89; 95% CI 1.03 to 6.75), and blood level of BNP/NT-proBNP (SMD -1.73; 95% CI -2.43 to -1.03). Conclusions: Adjuvant treatment with SFI can achieve additional benefits in improving quality of life and exercise tolerance in patients with CHF. These beneficial effects of SFI may correlate with its improving cardiac function. However, our findings should be interpreted with presence of significant heterogeneity and suboptimal quality of the analyzed trials.

3.
IUBMB Life ; 71(11): 1729-1739, 2019 11.
Article in English | MEDLINE | ID: mdl-31317653

ABSTRACT

This study aims to evaluate the efficacy of lysyl oxidase (LOX) inhibition in regulating rat myocardial fibrosis and chronic heart failure (CHF) and to validate the regulation of LOX by TGF-ß1/Smad2/3 signaling in this process. A rat model of CHF was established by abdominal aortic coarctation. The renin-angiotensin-aldosterone system (RAAS) indexes (PRA, ACE2, Ang II, and ALD), cardiac function indicators (LVEF, LVFS, SAP, DAP, and LVEDP), ventricular remodeling- and fibrosis-related indicators (hydroxyproline, collagen deposition,and MMP-2/9), and morphological changes of myocardial tissues were examined. Rat cardiac fibroblasts (RCFs) were used in vitro assays. CHF patients showed increased LOX activity, accompanied by activated RAAS and TGF-ß1. Furthermore, inhibition of LOX by ß-aminopropionitrile (BAPN) mitigated the RAAS activation and attenuated cardiac dysfunction, ventricular remodeling, myocardial fibrosis, and collagen deposition in CHF rats. Moreover, TGF-ß1 signaling diminished the LOX inhibition-mediated antiheart failure effect. Further assays showed that TGF-ß1/Smad2/3 signaling increased expression of c-jun (AP-1 transcription factor subunit), which transcriptionally induced LOX expression. Additionally, BAPN abrogated the TGF-ß1-mediated increase in cell proliferation and levels of MMP-2/9 and collagen I/III in RCFs. In conclusion, LOX can be induced by TGF-ß1/Smad/AP-1 signaling and LOX inhibition attenuates rat myocardial fibrosis and CHF.


Subject(s)
Cardiomyopathies/pathology , Fibrosis/pathology , Heart Failure/pathology , Protein-Lysine 6-Oxidase/metabolism , Smad2 Protein/metabolism , Smad3 Protein/metabolism , Transcription Factor AP-1/metabolism , Transforming Growth Factor beta1/metabolism , Animals , Cardiomyopathies/etiology , Cardiomyopathies/metabolism , Case-Control Studies , Fibrosis/etiology , Fibrosis/metabolism , Heart Failure/etiology , Heart Failure/metabolism , Humans , Phosphorylation , Protein-Lysine 6-Oxidase/genetics , Rats , Rats, Sprague-Dawley , Signal Transduction , Smad2 Protein/genetics , Smad3 Protein/genetics , Transcription Factor AP-1/genetics , Transforming Growth Factor beta1/genetics
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