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01 March 2022, Volume 20 Issue 2
    

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    Commentary
  • LIU Wei, MU Li-feng, WANG Zi-yu, YU Zhi-heng, ZHAI Suo-di, CAO Bao-shan
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 1-7. https://doi.org/10.3969/j.issn.1672-3384.2022.02.001
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    At present, different dosing regiments for programmed death receptor-1/programmed death ligand-1PD-1/PD-L1) monoclonal antibody (mAb) have been approved. On the basis of the initially approved body weight dosing regimen, fixed dosing and extended dosing interval regimen have been added. In this paper, the incidence of immune-related adverse reactions and economic evaluation of different PD-1/PD-L1 mAb dosing regiments were reviewed. The incidence of all-grade especially serious immune-related adverse reactions in the prolonged dosing interval regimen did not increase compared with the previous regimens, and it may have potential economic benefits and better suitability. During the corona virus disease 2019 (COVID-19) pandemic, the prolonged interval of administration has great positive clinical significance.
  • Review
  • SUN Bai-hao, LI Wen-long, GUAN Hao-yue, XU Ming-di
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 8-12. https://doi.org/10.3969/j.issn.1672-3384.2022.02.002
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    China is a big country producing generic drugs, with generic drugs accounting for about two-thirds of the whole chemical drug market. The quality control in generic drugs is particularly important. Impurity control is an important part of drug quality control. In terms of impurity control for generic drugs, we should not only pay attention to the impurities in the reference drugs, but also determine the possible impurities that need to be controlled according to the actual production process. In recent years, the industry has been increasingly concerned about genotoxic impurities in generic drugs. This article presents the sources and detection methods of genotoxic impurities in a macroscopic perspective, so as to provide a reference for the research and development of generic drugs in the industry.
  • Comment of new drugs
  • WANG Huan, ZHANG Cheng
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 13-17. https://doi.org/10.3969/j.issn.1672-3384.2022.02.003
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  • LIANG Nan, CHENG Mao-sheng, LIU Yang
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 18-21. https://doi.org/10.3969/j.issn.1672-3384.2022.02.004
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  • ZHANG Jiao, HUANG Ya-qun, BAI Ga-li, WEN Rui-ting
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 22-25. https://doi.org/10.3969/j.issn.1672-3384.2022.02.005
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  • Original Article
  • HU Xue, XIONG Ping-an, ZHANG Zhi-jun
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 26-31. https://doi.org/10.3969/j.issn.1672-3384.2022.02.006
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    Objective To investigate the effect of coenzyme Q10 pretreatment on the outcomes of in vitro fertilizing-embryo transfer (IVF-ET) in patients with polycystic ovary syndrome (PCOS). Methods A total of 100 PCOS patients who received IVF-ET treatment in Reproductive Medicine Center, Shiyan Taihe Hospital Affiliated Hospital of Hubei University of Medicine from August 2019 to August 2020 were randomly divided into the control group and the observation group.The observation group received coenzyme Q10 treatment for 3 months, and then started IVF-ET treatment. The general condition, metabolic level, process of superovulation, embryo laboratory outcome and pregnancy outcome of the two groups of patients were compared and analyzed. Results Fasting insulin (FINS) level and homeostasis model assessment of insulin resistance (HOMA-IR) in the observation group were significantly lower than those in the control group (P<0.05). The number of pronucleus(2PN) , the number of embryos in cleavage, the number of available embryos, the number of blastocysts, the rate of normal fertilization and the rate of excellent embryos in the observation group were all higher than those in the control group (P< 0.05). There were no significant differences in gonadotropin (GN) usage, hormone level on trigger day, number of eggs obtained, number of eggs at metaphase Ⅱ, blastocyst formation rate, number of embryos transferred, implantation rate and clinical pregnancy rate between the two groups (P > 0.05). Conclusion Coenzyme Q10 pretreatment can improve the fertilization rate and increase the number of high-quality embryos of PCOS patients undergoing IVF-ET. Although there is no statistical difference in clinical pregnancy rate, the results show an improvement tendency.
  • BIAN Meng, CHEN Shu-min, SHI Wei-zhong, SI Yan-bin, ZHAO Zhi-gang
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 32-38. https://doi.org/10.3969/j.issn.1672-3384.2022.02.007
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    Objective To analyze the application status of proton pump inhibitors(PPIs) in critical care departments of some hospitals in China from 2014 to 2020, to give reasonable suggestions and provide reference for clinical rational drug use. Methods The data were from sampling prescriptions of 94 institutions at all levels in 6 cities in China collected in “The Hospital Prescriptions Cooperation Project”. Analysis was carried out including the drug dosage, person times, drug selection, route of administration and preventive drug use. Results In this study, 369 922 prescriptions were collected. The statistical results showed that the use of PPIs in the critical medicine department of six cities increased year by year, and the rate of PPIs injections is higher than the of oral preparations. Preventive usage of PPIs accounted for 95.63% of the patients in the intensive care department, among which, 22.1% had indications, and 77.9% had no indications. Conclusion The clinical application of PPIs in the critical medicine department showed an increasing trend. There were some unreasonable problems such as improper route of administration and no indication of preventive usage. The use of PPIs in the critical medicine department should be standardized to make the use of PPIs more reasonable and economical.
  • ZHOU Jian, ZHAO Chun-yang, CAI Jia-yi, JIANG Ming-yan
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 39-46. https://doi.org/10.3969/j.issn.1672-3384.2022.02.008
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    Objective Network Meta-analysis was used to evaluate the efficacy and safety of perioperative anesthetics in reducing delirium after non-cardiac and non-craniocerebral surgery in adults. Methods The randomized controlled trial (RCT) literatures of perioperative anesthetics in reducing delirium undergoing non-cardiac and non-craniocerebral surgery from the database of CNKI, Wanfang, VIP, PubMed, Web of Science and Cochrane Library were selected. The quality of the included literatures were evaluated with RevMan 5.3 software. Stata16.0 software was used for the comparison of network Meta-analysis. Results A total of 44 RCTs studies and 7628 patients were included. Direct comparisons showed that compared with placebo (RR=0.48, 95%CI: 0.40-0.58, P<0.001), Propofol (RR=0.55, 95%CI: 0.38-0.78, P=0.001) and Midazolam (RR=0.25, 95%CI:0.17-0.36, P<0.001), Dexmedetomidine significantly reduced the incidence of postoperative delirium, which were consistent with network Meta-analysis. In terms of probability ranking, Dexmedetomidine seemed to be the best agent among all the treatments. In terms of adverse reactions, compared with placebo, Dexmedetomidine was associated with a higher incidence of perioperative hypotension (RR=1.21, 95%CI:1.09-1.34, P<0.001)and bradycardia (RR=1.47, 95%CI:1.25-1.72, P<0.001). Conclusion Dexmedetomidine can significantly reduce the risk of delirium after non-cardiac and non-craniocerebral surgery in adults. However, it has a higher risk of perioperative hypotension and bradycardia.
  • GU Yuan-yuan, ZHONG Zhao-hui, WANG Wan-yue, LIU Tian-tian, ZHANG Xiao, GONG Ying, CAO Jun-ling
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 47-54. https://doi.org/10.3969/j.issn.1672-3384.2022.02.009
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    Objective To investigate the mechanism of Trichosanthes Peel Injection in treating coronary heart disease (CHD) and angina pectoris through the network pharmacology-based approach. Methods The effective components in Trichosanthes Peel Injection were screened by using the Traditional Chinese Medicine Systems Pharmacology Database (TCMSP), and the gene names were predicted and given. The targets related to angina pectoris and shared targets were searched by the GeneCards database. Protein-gene interaction data were obtained by using the String database, and the interaction network was drawn by Cytoscape 3.7.2. GO enrichment analysis and KEGG pathway enrichment analysis were performed on the shared targets using the David database. Results The mechanism of Trichosanthes Peel Injection in the treatment of CHD and angina pectoris was mainly through 20 signal pathways of 5 active components and 69 targets (including 20 core targets). Besides, 137 biological processes, 33 cell components and 57 molecular functions were screened from 69 shared targets. The results of enrichment analysis showed that the injection mainly produced an effect on the cancer pathway, PPAR signaling pathways, proteoglycan pathway and prolactin signaling pathway. Conclusion By interacting with the core targets, the Trichosanthes Peel Injection may activate or block multiple signaling pathways to reduce inflammation, stabilize atherosclerotic plaques, regulate lipoprotein metabolism, alleviate angina, and improve endothelium proliferation.
  • LIN Zi-wei, ZUO Wei, YANG Yang, YU Jia-xin, ZHANG Bo
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 55-59. https://doi.org/10.3969/j.issn.1672-3384.2022.02.010
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    Objective To explore the clinical features of skin hyperpigmentation (SH) induced by Polymyxin B(PMB). Methods Case reports of Polymyxin B-induced skin hyperpigmentation (PMB-iSH) were collected by searching PubMed, Embase, ScienceDirect, Wiley Online Library, CNKI and Wanfang databases as of September 28th, 2021. The information of patients was extracted and analyzed descriptively. Results A total of 466 publications were screened, and 14 publications including 17 patients were eligible. The onset of PMB-iSH ranged from 2~15 days (average 7.4 days) after the first application of PMB. The main clinical symptoms include diffuse darkened skin color which prefers to happen on the head and neck area; or presents as the appearance of dark round spots. After the diagnosis of PMB-iSH, the administration of PMB was halted for 1 patient; 6 patients were lost to follow-up. Among 11 patients who were followed-up, 4 of them almost totally recovered at the follow-up time (the median time is 3.5 months after PMB withdrawal), among whom 3 patients were newborn or teenagers; 6 patients recovered at some extent after the same follow-up time, but not fully recovered to their original skin color; 1 patient showed no change about SH 5 months after PMB withdrawal. Conclusion PMB-iSH usually occurs within 15 days after the first application of PMB. The clinical symptoms include diffuse darkened skin color and dark round spots. PMB-iSH is reversible for most patients, but the time and extent of recovery maybe depend on the age. Some clinical interventions could be applied to reduce both physical and mental stress for patients.
  • ZHENG Zi-hui, ZHANG Bi-hua, LI Qiong, WANG Yang, ZHANG Bai-ge, MA Lin, LI Wen-ying, JIN Peng-fei
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 60-66. https://doi.org/10.3969/j.issn.1672-3384.2022.02.011
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    Objective To systematically evaluate the efficacy and safety of Compound Glycyrrhizin with Levocetirizine in the chronic urticaria(CU). Methods PubMed, Cochrane Library,Embase, CNKI and Wanfang databases were searched from the establishment of the database to January 31, 2022. Randomized controlled trials (RCTs) of Compound Glycyrrhizin combined with Levocetirizine in the treatment of CU published in Chinese journals were collected in the Chinese database, and journals were not in the English database. Two researchers extracted data, selected literatures, and evaluated the risk of bias in the included articles. Meta-analysis was performed using RevMan 5.4. Results A total of 8 RCTs were included in the analysis, involving 918 patients, 474 in the experimental group and 444 in the control group. Results of the Meta-analysis showed that the total effective rate in the CU(OR=6.14,95%CI:4.10 to 9.20, P<0.01), cure rate (OR=2.75,95%CI:2.04 to 3.72, P<0.01),marked effective rate(OR=1.58,95%CI:1.13 to 2.22, P<0.01),recurrence rate(OR=0.24, 95%CI:0.11 to 0.52, P<0.01),total symptom score (TSS) (SMD=-2.17,95%CI:-3.76 to -0.59,P<0.01) and dermatology life quality index(DLQI)(MD=-1.92,95%CI:-3.76 to -0.09,P<0.05) of the observation group were significantly better than the control group . In terms of adverse reactions, the observation group (OR=0.56,95%CI:0.35 to 0.90,P<0.05) was significantly lower than the control group. Conclusion The existing evidences suggest that Compound Glycyrrhizin with Levocetirizine is safer and more effective in the treatment of CU, compared to Levocetirizine alone. It is limited due to the quantity and quality of the included studies, and the above conclusions need to be verified by more high-quality RCTs.
  • CHEN Yue, DAI Shu-yue, LIU Lei
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 67-75. https://doi.org/10.3969/j.issn.1672-3384.2022.02.012
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    Objective To investigate the therapeutic regimens and pharmaceutical care of periprosthetic joint infection (PJI) caused by Mycobacterium abscessus complex (MABC) after arthroplasty. Methods CNKI,Wanfang, SinoMed, PubMed, ScienceDirect, Springer Link,Wiley Online Library databases were retrieved from establishment to September 30, 2020. To discuss the therapeutic regimens and pharmaceutical care of MABC PJI, data were analyzed on patient baseline information, surgical treatment and antimicrobial treatment. Results A total of 14 articles and 15 valid cases were included. Surgical treatment mainly consists of arthrocentesis, open debridement and two-stage revision. It was vital to conduct a prolonged and multidrug antimicrobial regimen according to in vitro drug susceptibility tests. The most common adverse drug effects were ototoxicity and nephrotoxicity of Amikacin followed by gastrointestinal reactions induced by Tigecycline. Conclusion MABC is a rare and intractable pathogen of PJI. Surgical procedures combined with antimicrobial drug therapy are needed. Patients are prone to encounter adverse drug reactions during prolonged therapy. Clinical pharmacists should actively provide pharmaceutical care.
  • SI Xia, LIU Yi, HUANG Lin, FENG Yu-fei
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 76-81. https://doi.org/10.3969/j.issn.1672-3384.2022.02.013
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    Objective To systematically evaluate the efficacy and safety of sequential therapy of Ginkgo biloba extract (GBE) in the treatment of sudden sensorineural hearing loss (SSNHL). Methods Embase, PubMed, Cochrane Library, Wanfang, CNKI and VIP databases were searched from the inception to October 31th, 2021, and trials about sequential therapy of GBE for SSNHL were selected (the study group was treated with sequential therapy of GBE, while the control group received conventional regimen). The quality of randomized controlled trial (RCT) and controlled clinical trial (CCT) were evaluated by using bias risk evaluation tool recommended by Cochrane and Newcastle Ottawa scale, respectively. RevMan 5.4 software was used for Meta-analysis. Results A total of 4 RCTs and 1 CCT involving 490 patients were included. Meta-analysis of RCTs indicated that total effective rate in study group was significantly higher than that of control group (RR=1.21, 95%CI: 1.08-1.36). Sub-group analysis as per therapeutic regimen showed that there was no significant difference in clinical cure rate between the two groups (RR=1.38, 95%CI: 0.31-6.07) when corticosteroids were contained in the control group. However, clinical cure rate in study group was significantly higher than that of control group (RR=1.41, 95%CI: 1.02-1.96) when the treatment regimen did not contain corticosteroids. There was no significant difference in the incidence of drug adverse reactions between the two groups (RR=0.58, 95%CI: 0.27-1.25). Descriptive analysis was used in one CCT that could not be combined, the results showed that the total effective rate of study group was better than control group (P<0.05), no serious adverse reactions were observed in the two groups. Conclusions Sequential therapy of GBE can effectively improve the total effective rate of SSNHL and has a good safety profile. Due to the small sample size and low quality of the included literatures, the above results still need to be further verified by high-quality clinical studies.
  • XU Kun, LU Yan-ping, WEI Lin, CHEN Lie-guang, ZHANG Pi-sheng
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 82-86. https://doi.org/10.3969/j.issn.1672-3384.2022.02.014
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    Objective This study was designed to investigate the application of pharmaceutical care network Europe (PCNE) classification system in identifying and solving drug related problems (DRP) in the physician-pharmacist joint clinic of hematology. Methods Patients who visited the physician-pharmacist joint clinic of hematology from September 1st 2019 to August 31st 2020 were collected. Problem, cause, intervention type, intervention acceptance rate and state of DRPs were analyzed. Results A total of 256 patients and 157 DRPs (0.61 DRPs per patient) were enrolled in this study. The main problem of DRPs was treatment effectiveness with a total of 81 cases (51.59%). The main cause was patient related with a total of 77 cases (43.75%). The main intervention type was at patient level with a total of 127 cases (52.92%). A total of 164 interventions were provided to physicians and patients by pharmacists among which 158 were accepted with the overall acceptance rate of 96.34%. Finally, 136 cases (86.62%) DRPs were solved. Conclusion Pharmacists intervention in DRPs using PCNE classification system in the physician-pharmacist joint clinic of hematology, which can improve the efficiency of identifying and solving DRPs and the effectiveness and safety of drug treatment, and also reflect the value of pharmacists in rational drug use.
  • Case research
  • QIAN Qing, XUE Dong, YAN Bo, FAN Min, HU Nan, CHEN Rong
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 87-90. https://doi.org/10.3969/j.issn.1672-3384.2022.02.015
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  • SI Rui-li, ZHOU Yong-fang, LIU Zong-zhan
    CLINICAL MEDICATION JOURNAL. 2022, 20(2): 91-92. https://doi.org/10.3969/j.issn.1672-3384.2022.02.016
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