1.Clinical Efficacy of Modified Huangqi Chifengtang in Treatment of IgA Nephropathy Patients and Exploration of Dose-effect Relationship of Astragali Radix
Xiujie SHI ; Meiying CHANG ; Yue SHI ; Ziyan ZHANG ; Yifan ZHANG ; Qi ZHANG ; Hangyu DUAN ; Jing LIU ; Mingming ZHAO ; Yuan SI ; Yu ZHANG
Chinese Journal of Experimental Traditional Medical Formulae 2025;31(2):9-16
ObjectiveTo explore the dose-effect relationship and safety of high, medium, and low doses of raw Astragali Radix in the modified Huangqi Chifengtang (MHCD) for treating proteinuria in immunoglobulin A (IgA) nephropathy, and to provide scientific evidence for the clinical use of high-dose Astragali Radix in the treatment of proteinuria in IgA nephropathy. MethodsA total of 120 patients with IgA nephropathy, diagnosed with Qi deficiency and blood stasis combined with wind pathogen and heat toxicity, were randomly divided into a control group and three treatment groups. The control group received telmisartan combined with a Chinese medicine placebo, while the treatment groups were given telmisartan combined with MHCD containing different doses of raw Astragali Radix (60, 30, 15 g). Each group contained 30 patients, and the treatment period was 12 weeks. Changes in 24-hour urinary protein (24 hUTP), traditional Chinese medicine (TCM) syndrome scores, effective rate, and renal function were observed before and after treatment. Safety was assessed by monitoring liver function and blood routine. ResultsAfter 12 weeks of treatment, 24 hUTP significantly decreased in the high, medium, and low-dose groups, as well as the control group (P<0.05, P<0.01). The TCM syndrome scores in the high, medium, and low-dose groups also significantly decreased (P<0.01). Comparisons between groups showed that the 24 hUTP in the high-dose group was significantly lower than in the medium, low-dose, and control groups (P<0.05, P<0.01), and the 24 hUTP in the medium-dose group was significantly lower than in the control group (P<0.05). The TCM syndrome scores in the high and medium-dose groups were significantly lower than in the low-dose and control groups (P<0.05, P<0.01). The total effective rates for proteinuria in the high, medium, low-dose, and control groups were 92.59% (25/27), 85.19% (23/27), 60.71% (17/28), and 57.14% (16/28), respectively. The effective rates in the high and medium-dose groups were significantly higher than in the low-dose and control groups (χ2=13.185, P<0.05, P<0.01). The effective rates for TCM syndrome scores in the high, medium, low-dose, and control groups were 88.89% (24/27), 81.48% (22/27), 71.43% (20/28), and 46.43% (13/28), respectively. The efficacy of TCM syndrome scores in the high and medium-dose groups was significantly higher than in the control group (χ2=14.053, P<0.01). Compared with pre-treatment values, there was no statistically significant difference in eGFR and serum creatinine in the high and medium-dose groups. However, eGFR significantly decreased in the low-dose and control groups after treatment (P<0.05), and serum creatinine levels increased significantly in the control group (P<0.05). No statistically significant differences were observed in urea nitrogen, uric acid, albumin, total cholesterol, triglycerides, liver function, and blood routine before and after treatment in any group. ConclusionThere is a dose-effect relationship in the treatment of IgA nephropathy with high, medium, and low doses of raw Astragali Radix in MHCD. The high-dose group exhibited the best therapeutic effect and good safety profile.
2.Validation and application of Chinese Clinical Context Assessment for Community Health in evidence-based hypertension medication management
Jingying ZHANG ; Fengpei ZHANG ; Hui TU ; Yanhong ZHAO ; Yingqian SONG ; Minxing OU ; Zhen YANG ; Xiujie ZHANG
Chinese Journal of Nursing 2025;60(10):1230-1237
Objective To translate the Context Assessment for Community Health(COACH)scale into Chinese,thereby providing a standardized measurement tool for context assessment in clinical evidence-based practice.Methods The scale was translated following the Brislin translation model,ultimately forming the Chinese version of the COACH scale.Using convenience sampling,584 healthcare professionals were recruited from 3 tertiary hospitals in Jiangxi,Henan,and Liaoning provinces and 2 community hospitals in Liaoning province from May to September 2024 to evaluate the reliability and validity of the scale.In October 2024,the Chinese version of COACH was applied to 44 healthcare professionals in a hypertension specialist ward of a provincial tertiary hospital.Results Of the 584 distributed questionnaires,519 valid questionnaires were collected(the effective response rate of 88.87%).The Chinese version consists of 7 dimensions with 42 items.The overall Cronbach's α coefficient was 0.975;the McDonald's omega coefficient was 0.979;split-half reliability was 0.808,and the test-retest reliability was 0.917.The scale-content validity index/average was 0.950,and the scale-content validity index/universal agreement was 0.980,with item-content validity index ranging from 0.775 to 1.000.Exploratory factor analysis extracted 7 factors,accounting for 79.260%of the cumulative variance,with factor loadings ranging from 0.569 to 0.954.Confirmatory factor analysis showed good model fit.The preliminary application results showed that the total score of the scale was 185.18±17.82.The correlation coefficients between dimensions and total score ranged from 0.116 to 0.905.Conclusion The Chinese version of the COACH scale demonstrates good reliability and validity,making it suitable as a context measurement tool for implementation research at different stages in clinical and public health settings.
3.E-health literacy for patients with cardiovascular disease: a scoping review
Qian WANG ; Jingying ZHANG ; Minxing OU ; Jingjing ZHAO ; Xiujie ZHANG
Chinese Journal of Modern Nursing 2025;31(12):1657-1664
Objective:To carry out a scoping review on eHealth literacy in patients with cardiovascular disease to sort out eHealth literacy from four aspects of concepts, assessment tools, influencing factors and interventions, with a view to informing future research and practice.Methods:Based on Arksey and O'Malley's framework for reporting scoping reviews, the literature on eHealth literacy in patients with cardiovascular disease was systematically searched in PubMed, Web of Science, Embase, Cochrane Library, CINAHL, China National Knowledge Infrastructure, VIP, Wanfang Data, and China Biomedical Database. The search period was from database establishment to May 3, 2024. Literature was screened, summarized and analyzed.Results:A total of 23 papers were included. The concepts and theoretical frameworks on eHealth literacy had their own focus, but no consensus was reached. The most commonly used tool to assess eHealth literacy in patients with cardiovascular disease was the eHealth Literacy Scale. The influencing factors included four aspects of demographic sociological and disease-related factors, psycho-cognitive factors, eHealth literacy knowledge and skills, and other factors. Interventions to improve eHealth literacy among patients with cardiovascular disease primarily included eHealth literacy training and use of portal-related digital toolkit.Conclusions:Currently there is no specific assessment tool for eHealth literacy for cardiovascular disease patients. In the future, eHealth literacy assessment tools need to be revised and improved according to the population characteristics and cultural background of cardiovascular disease patients. E-health literacy among patients with cardiovascular disease is at a moderately low level and is influenced by multiple factors. The influencing factors can be analyzed in depth through large-sample cross-sectional studies or longitudinal studies, and then a variety of intervention programs can be constructed at home or in the community with the help of multimedia and apps, with a view to improving the e-health literacy of patients with cardiovascular diseases.
4.Validation and application of Chinese Clinical Context Assessment for Community Health in evidence-based hypertension medication management
Jingying ZHANG ; Fengpei ZHANG ; Hui TU ; Yanhong ZHAO ; Yingqian SONG ; Minxing OU ; Zhen YANG ; Xiujie ZHANG
Chinese Journal of Nursing 2025;60(10):1230-1237
Objective To translate the Context Assessment for Community Health(COACH)scale into Chinese,thereby providing a standardized measurement tool for context assessment in clinical evidence-based practice.Methods The scale was translated following the Brislin translation model,ultimately forming the Chinese version of the COACH scale.Using convenience sampling,584 healthcare professionals were recruited from 3 tertiary hospitals in Jiangxi,Henan,and Liaoning provinces and 2 community hospitals in Liaoning province from May to September 2024 to evaluate the reliability and validity of the scale.In October 2024,the Chinese version of COACH was applied to 44 healthcare professionals in a hypertension specialist ward of a provincial tertiary hospital.Results Of the 584 distributed questionnaires,519 valid questionnaires were collected(the effective response rate of 88.87%).The Chinese version consists of 7 dimensions with 42 items.The overall Cronbach's α coefficient was 0.975;the McDonald's omega coefficient was 0.979;split-half reliability was 0.808,and the test-retest reliability was 0.917.The scale-content validity index/average was 0.950,and the scale-content validity index/universal agreement was 0.980,with item-content validity index ranging from 0.775 to 1.000.Exploratory factor analysis extracted 7 factors,accounting for 79.260%of the cumulative variance,with factor loadings ranging from 0.569 to 0.954.Confirmatory factor analysis showed good model fit.The preliminary application results showed that the total score of the scale was 185.18±17.82.The correlation coefficients between dimensions and total score ranged from 0.116 to 0.905.Conclusion The Chinese version of the COACH scale demonstrates good reliability and validity,making it suitable as a context measurement tool for implementation research at different stages in clinical and public health settings.
5.E-health literacy for patients with cardiovascular disease: a scoping review
Qian WANG ; Jingying ZHANG ; Minxing OU ; Jingjing ZHAO ; Xiujie ZHANG
Chinese Journal of Modern Nursing 2025;31(12):1657-1664
Objective:To carry out a scoping review on eHealth literacy in patients with cardiovascular disease to sort out eHealth literacy from four aspects of concepts, assessment tools, influencing factors and interventions, with a view to informing future research and practice.Methods:Based on Arksey and O'Malley's framework for reporting scoping reviews, the literature on eHealth literacy in patients with cardiovascular disease was systematically searched in PubMed, Web of Science, Embase, Cochrane Library, CINAHL, China National Knowledge Infrastructure, VIP, Wanfang Data, and China Biomedical Database. The search period was from database establishment to May 3, 2024. Literature was screened, summarized and analyzed.Results:A total of 23 papers were included. The concepts and theoretical frameworks on eHealth literacy had their own focus, but no consensus was reached. The most commonly used tool to assess eHealth literacy in patients with cardiovascular disease was the eHealth Literacy Scale. The influencing factors included four aspects of demographic sociological and disease-related factors, psycho-cognitive factors, eHealth literacy knowledge and skills, and other factors. Interventions to improve eHealth literacy among patients with cardiovascular disease primarily included eHealth literacy training and use of portal-related digital toolkit.Conclusions:Currently there is no specific assessment tool for eHealth literacy for cardiovascular disease patients. In the future, eHealth literacy assessment tools need to be revised and improved according to the population characteristics and cultural background of cardiovascular disease patients. E-health literacy among patients with cardiovascular disease is at a moderately low level and is influenced by multiple factors. The influencing factors can be analyzed in depth through large-sample cross-sectional studies or longitudinal studies, and then a variety of intervention programs can be constructed at home or in the community with the help of multimedia and apps, with a view to improving the e-health literacy of patients with cardiovascular diseases.
6.Research progress on the improvement mechanism of traditional Chinese medicine compounds and active ingredients in schizophrenia
Xinhui YAO ; Yonghou ZHAO ; Jianbo CHAI ; Ming YU ; Xiujie QU
China Pharmacy 2024;35(9):1151-1156
Schizophrenia has various obstacles in cognition, thinking, emotion, behavior and other aspects; it belongs to the category of “madness” in traditional Chinese medicine (TCM). Once schizophrenia occurs, multiple factors are often intertwined, and a single therapy is difficult to be effective. At present, TCM compounds and active ingredients have significant effects in the clinical treatment of schizophrenia, which is an important direction for the development of new drugs for schizophrenia. This article summarizes the molecular mechanism of TCM compounds and active ingredients in the treatment of schizophrenia. It is found that Wendan decoction and Yudian decoction can inhibit the apoptosis of hippocampal cells by activating BDNF/TrKB/CREB signaling pathway; quercetin and icariin can promote neural development and regeneration by activating NMDA/ERK signaling pathway; Wendan decoction and icariin can maintain neural cell homeostasis by activating PI3K/AKT signaling pathway; Bushen zhuangyang capsule can enhance learning and memory abilities by activating CaMKⅡ signaling pathway; formulas such as Huatan huoxue tongzhi formula can enhance intercellular information transmission by inhibiting PKC signaling pathway; α-humulene and others can restore nerve cell function by inhibiting NRG1/ErbB4 signaling pathway. TCM compounds and active ingredients can improve schizophrenia by intervening in the above-mentioned signaling pathways.
7.Diagnostic value of cell-free DNA detection in tuberculous pleurisy
CHENG Liang ; HUA Shaopeng ; JIANG Yanping ; JIA Xiujie ; HU Xiaofang ; ZHAO Xinguo
China Tropical Medicine 2024;24(2):162-
Objective To assess the diagnostic efficacy of the cell-free Mycobacterium tuberculosis DNA testing (CF-TB) in tuberculous pleurisy. Methods A total of 71 patients diagnosed with tuberculous pleurisy and 35 patients with non-tuberculous pleurisy were selected from the Fifth People's Hospital of Wuxi between January to December 2022. The standard pleural puncture was conducted to collect pleural effusion, which was then utilized for Mycobacterium tuberculosis culture, GeneXpert Mycobacterium tuberculosis/rifampicin resistance (GeneXpert MTB/RIF), CF-TB, and adenosine deaminase (ADA) testing. Blood samples were subjected to tuberculosis infection T-cell spotting test (T-SPOT.TB) assay. The receiver operator characteristic curve (ROC) was applied to obtain the optimal cut-off value for pleural fluid CF-TB and to compare the diagnostic performance of CF-TB with other methods. Data analysis was conducted using SPSS 22.0 software, with statistical significance defined as P<0.05. Results The ROC curve analysis determined that the optimal cycle threshold (Ct) value for diagnosing tuberculous pleurisy using CF-TB in pleural fluid was 38.489, with a sensitivity of 91.5% and specificity of 97.1%. In comparison, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of T-SPOT.TB and pleural fluid ADA in diagnosing tuberculous pleurisy were 86.0%, 71.4%, 86.0%, 71.4%, 81.1%, and 55.0%, 91.4%, 92.9%, 50.8%, 67.0%, respectively, all of which were lower than the diagnostic efficiency of CF-TB. Furthermore, the specificity of pleural fluid CF-TB in diagnosing tuberculous pleurisy (97.1%) was not significantly different from GeneXpert MTB/RIF (100%) and Mycobacterium tuberculosis culture (100%), but its sensitivity (91.5%) was significantly higher than both GeneXpert MTB/RIF (19.7%) and Mycobacterium tuberculosis culture (28.2%), with a statistically significant difference (P<0.001). Conclusions Compared to the conventional gold standard for diagnosing tuberculous pleurisy, CF-TB exhibits a higher sensitivity and its specificity is superior to that of tuberculosis immunological test. Consequently, CF-TB can serve as a valuable complement to other traditional detection methods in aiding the diagnosis of tuberculous pleurisy.
8.Long-term hypomethylating agents in patients with myelodysplastic syndromes: a multi-center retrospective study
Xiaozhen LIU ; Shujuan ZHOU ; Jian HUANG ; Caifang ZHAO ; Lingxu JIANG ; Yudi ZHANG ; Chen MEI ; Liya MA ; Xinping ZHOU ; Yanping SHAO ; Gongqiang WU ; Xibin XIAO ; Rongxin YAO ; Xiaohong DU ; Tonglin HU ; Shenxian QIAN ; Yuan LI ; Xuefen YAN ; Li HUANG ; Manling WANG ; Jiaping FU ; Lihong SHOU ; Wenhua JIANG ; Weimei JIN ; Linjie LI ; Jing LE ; Wenji LUO ; Yun ZHANG ; Xiujie ZHOU ; Hao ZHANG ; Xianghua LANG ; Mei ZHOU ; Jie JIN ; Huifang JIANG ; Jin ZHANG ; Guifang OUYANG ; Hongyan TONG
Chinese Journal of Hematology 2024;45(8):738-747
Objective:To evaluate the efficacy and safety of hypomethylating agents (HMA) in patients with myelodysplastic syndromes (MDS) .Methods:A total of 409 MDS patients from 45 hospitals in Zhejiang province who received at least four consecutive cycles of HMA monotherapy as initial therapy were enrolled to evaluate the efficacy and safety of HMA. Mann-Whitney U or Chi-square tests were used to compare the differences in the clinical data. Logistic regression and Cox regression were used to analyze the factors affecting efficacy and survival. Kaplan-Meier was used for survival analysis. Results:Patients received HMA treatment for a median of 6 cycles (range, 4-25 cycles) . The complete remission (CR) rate was 33.98% and the overall response rate (ORR) was 77.02%. Multivariate analysis revealed that complex karyotype ( P=0.02, OR=0.39, 95% CI 0.18-0.84) was an independent favorable factor for CR rate. TP53 mutation ( P=0.02, OR=0.22, 95% CI 0.06-0.77) was a predictive factor for a higher ORR. The median OS for the HMA-treated patients was 25.67 (95% CI 21.14-30.19) months. HMA response ( P=0.036, HR=0.47, 95% CI 0.23-0.95) was an independent favorable prognostic factor, whereas complex karyotype ( P=0.024, HR=2.14, 95% CI 1.10-4.15) , leukemia transformation ( P<0.001, HR=2.839, 95% CI 1.64-4.92) , and TP53 mutation ( P=0.012, HR=2.19, 95% CI 1.19-4.07) were independent adverse prognostic factors. There was no significant difference in efficacy and survival between the reduced and standard doses of HMA. The CR rate and ORR of MDS patients treated with decitabine and azacitidine were not significantly different. The median OS of patients treated with decitabine was longer compared with that of patients treated with azacitidine (29.53 months vs 20.17 months, P=0.007) . The incidence of bone marrow suppression and pneumonia in the decitabine group was higher compared with that in the azacitidine group. Conclusion:Continuous and regular use of appropriate doses of hypomethylating agents may benefit MDS patients to the greatest extent if it is tolerated.
9.A Single-Center Retrospective Cohort Study of Yinqiao Piwen Powder for the Treatment of Patients with Mild Corona Virus Disease 2019
Qianqian ZHAO ; Xiujie LYU ; Hanxiao LYU
Journal of Zhejiang Chinese Medical University 2024;48(12):1517-1524
[Objective]To evaluate the effectiveness of Yinqiao Piwen Powder,an empirical formula,in the treatment of mild cases of corona virus disease 2019(COVID-19) infection.[Methods]A single-center retrospective cohort study was adopted. A total of 595 patients with mild COVID-19 infection who attended Zhejiang Provincial Hospital of Traditional Chinese Medicine from December 18 to 23,2022 were included in this study and then divided into western medicine group (WM),traditional Chinese medicine group (TCM) and integrated Chinese and western medicine group (TCM-WM) based on their medication,with 153 cases,144 cases and 298 cases in each respectively. The WM group received routine treatment of western medicine according to the Diagnosis and Treatment Protocol for COVID-19 Patients (Tentative 10th Edition),the TCM group received Yinqiao Piwen powder treatment,and the TCM-WM group received Yinqiao Piwen Powder treatment on the basis of the treatment of the WM group. After 14 days,the therapeutic effect of patients was evaluated. Specifically,the baseline characteristics,clinical symptoms and symptom relief time of the patients were collected,the TCM symptom scores were estimated,and the distribution of symptoms and efficacy distribution after treatment in each group were analyzed.[Results]The most common symptoms in patients with mild COVID-19 infection were fever,cough,sputum,fatigue,body aches,sore throat,nasal congestion and runny nose. On the efficacy distribution,the markedly effective rate of the TCM-WM group was significantly higher than that of the WM group,which were both significantly different(x2=14.022,P<0.001) After treatment,the total TCM symptom scores of all three groups were significantly decreased compared with pre-treatment,indicating a great relief in the clinical symptoms in all groups,with a statistically significant difference (P<0.001). Additionally,the median number of the rate of reduction of TCM symptom scores in the TCM-WM group was 100.00(93.21,100.00),higher than the TCM group[100.00(92.15,100.00)]and the WM group[100.00(78.95,100.00)],and showed statistical difference (P<0.05). The differences of TCM symptom scores of three groups between the pre-treatment and post-treatment were significant (P<0.05),and the TCM-WM group changed the most in the scores. Besides,after correction for age and pre-treatment symptom scores,the differences in post-treatment TCM symptom scores among the three groups were still statistically significant ( P<0.05). Moreover,the differences among the three groups in the symptom relief time of sore throat,cough,sputum and fatigue were statistically significant(P<0.05).[Conclusion]Compared with the western medicine treatment alone,the other two treatments achieved better clinical results in improving the efficacy,reducing the TCM symptom scores and shortening the symptom relief time. The results of our study can provide evidence-based medical proof for the benefits of TCM in the prevention and treatment of epidemics.
10.A Single-Center Retrospective Cohort Study of Yinqiao Piwen Powder for the Treatment of Patients with Mild Corona Virus Disease 2019
Qianqian ZHAO ; Xiujie LYU ; Hanxiao LYU
Journal of Zhejiang Chinese Medical University 2024;48(12):1517-1524
[Objective]To evaluate the effectiveness of Yinqiao Piwen Powder,an empirical formula,in the treatment of mild cases of corona virus disease 2019(COVID-19) infection.[Methods]A single-center retrospective cohort study was adopted. A total of 595 patients with mild COVID-19 infection who attended Zhejiang Provincial Hospital of Traditional Chinese Medicine from December 18 to 23,2022 were included in this study and then divided into western medicine group (WM),traditional Chinese medicine group (TCM) and integrated Chinese and western medicine group (TCM-WM) based on their medication,with 153 cases,144 cases and 298 cases in each respectively. The WM group received routine treatment of western medicine according to the Diagnosis and Treatment Protocol for COVID-19 Patients (Tentative 10th Edition),the TCM group received Yinqiao Piwen powder treatment,and the TCM-WM group received Yinqiao Piwen Powder treatment on the basis of the treatment of the WM group. After 14 days,the therapeutic effect of patients was evaluated. Specifically,the baseline characteristics,clinical symptoms and symptom relief time of the patients were collected,the TCM symptom scores were estimated,and the distribution of symptoms and efficacy distribution after treatment in each group were analyzed.[Results]The most common symptoms in patients with mild COVID-19 infection were fever,cough,sputum,fatigue,body aches,sore throat,nasal congestion and runny nose. On the efficacy distribution,the markedly effective rate of the TCM-WM group was significantly higher than that of the WM group,which were both significantly different(x2=14.022,P<0.001) After treatment,the total TCM symptom scores of all three groups were significantly decreased compared with pre-treatment,indicating a great relief in the clinical symptoms in all groups,with a statistically significant difference (P<0.001). Additionally,the median number of the rate of reduction of TCM symptom scores in the TCM-WM group was 100.00(93.21,100.00),higher than the TCM group[100.00(92.15,100.00)]and the WM group[100.00(78.95,100.00)],and showed statistical difference (P<0.05). The differences of TCM symptom scores of three groups between the pre-treatment and post-treatment were significant (P<0.05),and the TCM-WM group changed the most in the scores. Besides,after correction for age and pre-treatment symptom scores,the differences in post-treatment TCM symptom scores among the three groups were still statistically significant ( P<0.05). Moreover,the differences among the three groups in the symptom relief time of sore throat,cough,sputum and fatigue were statistically significant(P<0.05).[Conclusion]Compared with the western medicine treatment alone,the other two treatments achieved better clinical results in improving the efficacy,reducing the TCM symptom scores and shortening the symptom relief time. The results of our study can provide evidence-based medical proof for the benefits of TCM in the prevention and treatment of epidemics.

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