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1.
Int J Antimicrob Agents ; 62(2): 106857, 2023 Aug.
Article in English | MEDLINE | ID: covidwho-2326271

ABSTRACT

BACKGROUND: Nirmatrelvir-ritonavir (NMVr) is a recently developed antiviral agent for treating coronavirus disease 2019 (COVID-19); however, data describing its appropriate use are scarce. This study examined the prevalence of inappropriate use of NMVr in a Chinese hospital setting. METHODS: A multi-centre retrospective chart review was performed for all hospitalized patients who received NMVr between 15 December 2022 and 15 February 2023 in four university-affiliated hospitals in Hangzhou, China. A multi-disciplinary team of experts developed the evaluation criteria. A group of senior clinical pharmacists examined and verified the suitability of NMVr prescriptions. RESULTS: In total, 247 patients received NMVr during the study period, of which 13.4% (n=31) met all the criteria for appropriate use of NMVr. The main types of inappropriate use of NMVr were delayed initiation of treatment (n=147, 59.5%), no dose adjustment for moderate renal impairment (n=46, 18.6%), use in patients with severe-to-critical COVID-19 (n=49, 19.8%), presence of contra-indicated drug‒drug interactions with other medications (n=36, 14.6%), and prescription for patients without a confirmed diagnosis of COVID-19 (n=36, 14.6%). CONCLUSIONS: The proportion of inappropriate use of NMVr was particularly high in the Chinese hospital setting, highlighting the urgent need to improve the appropriate use of NMVr.

2.
Trials ; 22(1): 955, 2021 Dec 27.
Article in English | MEDLINE | ID: covidwho-2318366

ABSTRACT

BACKGROUND: Influenza can fall into three categories according to severity: mild influenza, severe influenza, and critical influenza. Severe influenza can result in critical illness and sometimes death particularly in patients with comorbidities, advanced age, or pregnancy. Neuraminidase inhibitors (NAIs) are the only antiviral drugs in widespread use for influenza. However, the effectiveness of NAIs against severe influenza is uncertain. New effective drugs or regimens are therefore urgently needed. Qiangzhu-qinggan (QZQG) formula has been found to be effective against influenza virus infection during long-term application in China, which lacks support of evidence-based clinical trial till now. This study is designed to assess the efficacy and safety of QZQG formula as an adjuvant therapy in adult patients with severe influenza. METHODS: This protocol is drawn up in accordance with the SPIRIT guidelines and CONSORT Extension for Chinese herbal medicine formulas. This is a randomized, placebo-controlled, double-blind, multicenter trial. Two hundred twenty-eight adults with severe influenza are randomly assigned in a 1:1 ratio to QZQG or placebo for 7 days. All participants need to receive 1 day of screening before randomization, 7 days of intervention, and 21 days of observation after randomization. The primary outcome is the proportion of clinical improvement, defined as the proportion of patients who met the criteria of 3 points or less in the seven-category ordinal scale or 2 points or less in National Early Warning Score 2 within 7 days after randomization. DISCUSSION: This is the first randomized, controlled, parallel, double-blind clinical trial to evaluate the efficacy and safety of traditional Chinese herbal formula granules as an adjuvant therapy in adult patients with severe influenza. This study aims to redefine the value of traditional Chinese herbal medicines in the treatment of virus-related respiratory infectious diseases and serves as an example of evidence-based clinical trials of other Chinese herbal medicines.


Subject(s)
Drugs, Chinese Herbal , Influenza, Human , Adult , Antiviral Agents/adverse effects , Combined Modality Therapy , Double-Blind Method , Drugs, Chinese Herbal/adverse effects , Humans , Influenza, Human/diagnosis , Influenza, Human/drug therapy , Multicenter Studies as Topic , Randomized Controlled Trials as Topic , Treatment Outcome
3.
MedComm (2020) ; 3(4): e173, 2022 Dec.
Article in English | MEDLINE | ID: covidwho-2041224

ABSTRACT

Emerging evidence indicates that resolution of inflammation is a critical and dynamic endogenous process for host tissues defending against external invasive pathogens or internal tissue injury. It has long been known that autoimmune diseases and chronic inflammatory disorders are characterized by dysregulated immune responses, leading to excessive and uncontrol tissue inflammation. The dysregulation of epigenetic alterations including DNA methylation, posttranslational modifications to histone proteins, and noncoding RNA expression has been implicated in a host of inflammatory disorders and the immune system. The inflammatory response is considered as a critical trigger of epigenetic alterations that in turn intercede inflammatory actions. Thus, understanding the molecular mechanism that dictates the outcome of targeting epigenetic regulators for inflammatory disease is required for inflammation resolution. In this article, we elucidate the critical role of the nuclear factor-κB signaling pathway, JAK/STAT signaling pathway, and the NLRP3 inflammasome in chronic inflammatory diseases. And we formulate the relationship between inflammation, coronavirus disease 2019, and human cancers. Additionally, we review the mechanism of epigenetic modifications involved in inflammation and innate immune cells. All that matters is that we propose and discuss the rejuvenation potential of interventions that target epigenetic regulators and regulatory mechanisms for chronic inflammation-associated diseases to improve therapeutic outcomes.

4.
Chinese Journal of Information on Traditional Chinese Medicine ; 27(8):15-17, 2020.
Article in Chinese | CAB Abstracts | ID: covidwho-1319773

ABSTRACT

Traditional Chinese Medicine (TCM) practitioners have deepened their understanding of the disease theory with the gradually increasing degree of clinical intervention of coronavirus disease 2019 (COVID-19). Especially, "Dampness Toxin" as the core of TCM pathogenesis has reached consensus. However, the comprehension on the pathogenesis and transmission laws of COVID-19 still need to be quickly improved in order to promote optimization to form a more effective common regimen for diagnosis and treatment of TCM on COVID-19. The author's team based on first-line clinical and academic data verified the cause and proposed that "cold-dampness and retained fluid blocking lung with fire deficiency of Mingmen" be important pathogenesis of severe patients with COVID-19. And the treatment principle should follow "ruling water with fire, and treating tri-jiao simultaneously". The prescription should refer to Shegan Mahuang Decoction, Zhenwu Decoction, Fuzi Lizhong Decoction and other formulas to warm tri- jiao, which aims to consolidate the essence of human body. "Detoxification, dredging six-Fu organs and diuresis" also need to be considered to alleviate the symptoms at the same time. This regimen reflects the consideration of both the symptoms and causes, the combination of cold and warm medicinal herbs, tonification and purgation in combination, flexibility in syndrome differentiation and prescription and careful grasp of the balance of the property of herbs, which can provide a reference for clinical diagnosis and treatment on COVID-19.

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