1.Clinical observation of dupilumab in the treatment of severe asthma-COPD overlap
Honghua JI ; Wangfei JI ; Qilin ZHU
China Pharmacy 2025;36(20):2571-2576
OBJECTIVE To investigate the clinical efficacy and safety of dupilumab in patients with severe asthma-chronic obstructive pulmonary disease (COPD) overlap (ACO). METHODS A retrospective analysis was conducted on 150 patients with severe ACO treated at Nantong Third People’s Hospital during Jan. 2022-Dec. 2023. Patients were divided into the control group [conventional therapy with inhaled corticosteroids (ICS)+long-acting beta-2 agonists (LABA)+long-acting muscarinic anticholinergic (LAMA), n=90] and the observation group (conventional therapy plus dupilumab, n=60) based on different treatment regimens. Propensity score matching (PSM) was performed at a ratio of 1.5∶1. Symptom control scores [Asthma Control Test (ACT) score, COPD Assessment Test (CAT) score] and pulmonary function parameters [forced vital capacity (FVC), forced expiratory volume in 1 second (FEV1), the FEV1 in percentage of predicted value (FEV1%pred), the ratio of FEV1 and FVC (FEV1/FVC), peak expiratory flow (PEF) and maximal mid-expiratory flow (MMEF)] before treatment and at 1, 3, and 12 months after treatment, as well as the levels of biomarkers [peripheral blood eosinophil (EOS) count, immunoglobulin E (IgE), C-reactive protein (CRP), fractional exhaled nitric oxide (FeNO)], annual acute exacerbation frequency, quality-of-life scores [Asthma Quality of Life Questionnaire (AQLQ) score, St George’s Respiratory Questionnaire (SGRQ) score, and Medical Outcomes Study 36-item Short Form Health Survey (SF-36) score] before treatment and 12 months after treatment, and the occurrence of adverse reactions were compared. RESULTS After PSM, 120 patients were included, involving 72 cases in the control group and 48 cases in the observation group. Compared with before treatment, both groups showed significant improvements in ACT scores at 1, 3, and 12 months after treatment, FVC, FEV1, FEV1%pred (except at 3 months after treatment in the control group), (except at 3 months after treatment in the control group), PEF (except at 3 and 12 months after treatment in the control group) and MMEF (including at 1 month after treatment in the observation group) at 3 and 12 months after treatment, as well as AQLQ and SF-36 scores at 12 months after treatment (P<0.05). CAT scores at 1, 3 and 12 months after treatment, annual acute exacerbation frequency and SGRQ score at 12 months after treatment, FeNO levels at 12 months after treatment in the control group, as well as EOS count, IgE, CRP and FeNO levels at 12 months after treatment in the observation group were significantly reduced (P<0.05). The improvements of above indicators in the observation group were mostly greater than in the control group (P<0.05). The incidence of adverse reactions did not differ significantly between the two groups (P>0.05). CONCLUSIONS Dupilumab provides superior efficacy over conventional therapy in improving clinical symptoms, pulmonary function, and quality of life, while reducing biomarker levels in patients with severe ACO, with a comparable safety profile to standard therapy.
2. To explore the treatment mechanism of Wenpi decoction on ulcer colitis based on integrative pharmacology of traditional Chinese medicine platform
Honghua ZHANG ; Shuling WANG ; Bin YU ; Yanan ZHANG ; Xumin JI
International Journal of Traditional Chinese Medicine 2019;41(11):1225-1230
Objective:
The active components and potential targets were predicted and confirmed to explore the possible mechanism of
3.The effects of levosimendan on prognosis and circulatory function of sepsis patients: a Meta-analysis
Honghua ZHANG ; Guoxiu ZHANG ; Jie LI ; Xiaolei WEI ; Dahuan LI ; Ji YUAN
Chinese Journal of Integrated Traditional and Western Medicine in Intensive and Critical Care 2018;25(2):120-126
Objective To evaluate the effect of levosimendan on prognosis and circulation disorders of sepsis patients. Methods With the guidance of these following Chinese or English key words, such as sepsis, severe sepsis, septic shock, simendan, levosimendan, etc., some of Chinese and foreign published literatures on randomized controlled trials (RCTs) concerning the effects of levosimendan on the prognosis and circulatory function of septic patients were searched through China National Knowledge Infrastructure (CNKI) internet, VIP and Wanfang Databases, China Biomedicine Database (CMB), Pubmed in American National library, Holland Medical Abstract Database (Embase), Cochrane Library, etc databases, from the creation of above various databases to May 2017. The quality of the collected RCTs was evaluated by modified Jadad score; Revman 5.3 software was used to carry out Meta analysis; the publication bias was assessed by the funnel plots. Results A total of 18 RCTs, 9 in Chinese and 9 in English, but only half of the literatures were of high quality, and the other 9 of low quality, containing 688 cases in control group and 704 cases in experimental group were ultimately enrolled in this analysis. The Meta analyses showed that there was no statistical significant difference in the mortality between the experimental group and the control group [relative risk (RR) = 0.92, 95% confidence interval (95%CI) = 0.80 - 1.06, P = 0.27]; compared with control group, the time of stay in ICU was shortened [mean difference (MD) = -2.02, 95%CI = -2.90 to -1.13, P < 0.000 01], cardic output index was increased (MD = 0.63, 95%CI = 0.39 - 0.87, P < 0.000 01), and blood lactate level was decreased (MD = -1.37, 95%CI = -1.51 to-1.23, P < 0.000 01) in the experimental group, being significantly improved after levosimendan therapy. The funnel map evaluation showed that there might be a certain bias in the publication of the literature. Conclusion Levosimendan can improve circulatory disorders and reduce the time of stay in ICU for septic patients, but can not reduce their mortality.

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