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Combinations of Fe tablets and dragon fruit and combinations of Fe tablets and date straw on increasing hemoglobin levels in adolescent women with anemia 铁片与火龙果联合用药及铁片与椰枣秸秆联合用药对青少年贫血妇女血红蛋白水平的影响
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0013
D. Damayanti, Zuriyati Bawirza, Taufik Hidayat, S. Wardoyo
Abstract Anemia is a health problem related to the extensive presence of a variety of noncommunicable diseases in developing countries. Indeed, the prevalence of anemia in Indonesia in women of childbearing age (aged 15-49 years) in 2019 was around 29.9%; in West Kalimantan in 2018, it was 23.8%. The rate of anemia in young women can be overcome by increasing hemoglobin levels. One approach is to enhance the consumption of dragon fruit or date palm juice which can increase hemoglobin levels. This research aims to determine the effectiveness of giving a combination of Fe tablets and dragon fruit or a combination of Fe tablets with date palm juice on hemoglobin levels in anemic adolescent girls. The design of this study was a True Experiment with pre-test and post-test control groups. Research respondents were anemic adolescent girls, a total of 32 people, with 16 in each group. With regard to the hemoglobin levels before and after administration of Fe tablets and dragon fruit, based on the paired t-test, the mean difference was 4.32 g/dl, with P-Value = 0.000. Thus, there is effectiveness in this intervention group. In the combination group of Fe tablets and date palm juice, the mean difference was 3.062 g/dl. P-Value = 0.001 (P<0.05). Hence, there is effectiveness in enhancing hemoglobin levels in this intervention group. Applying an independent t-test to determine the difference in the effectiveness of the two interventions revealed a P-value = 0.054, meaning that there was no significant difference between the two interventions in increasing hemoglobin levels.
贫血是发展中国家与多种非传染性疾病广泛存在相关的健康问题。事实上,2019年印度尼西亚育龄妇女(15-49岁)的贫血患病率约为29.9%;在2018年的西加里曼丹,这一比例为23.8%。年轻女性的贫血率可以通过提高血红蛋白水平来克服。一种方法是增加火龙果或椰枣汁的摄入量,这可以提高血红蛋白水平。本研究旨在确定铁片和火龙果的组合或铁片和椰枣汁的组合对贫血少女血红蛋白水平的影响。本研究采用真实实验设计,分为前测组和后测组。调查对象为患有贫血症的青春期少女,共32人,每组16人。服用铁片和火龙果前后的血红蛋白水平,经配对t检验,平均差异为4.32 g/dl, p值= 0.000。因此,这个干预组是有效的。铁片与椰枣汁联合组平均差异为3.062 g/dl。P值= 0.001 (P<0.05)。因此,该干预组在提高血红蛋白水平方面是有效的。应用独立t检验来确定两种干预措施的有效性差异,p值= 0.054,这意味着两种干预措施在提高血红蛋白水平方面没有显著差异。
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引用次数: 1
The monoamine theory of depression as a target to effective pharmacotherapy 单胺理论将抑郁症作为有效药物治疗的靶点
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0019
Tomasz Karabin, G. Biała, M. Kruk-Slomka
Abstract Depression is one of the greatest current mental disorders. Depressive disorder may affect everyone and it causes difficulties in social functioning and may lead to death via suicide. Depression is a serious problem because number of its cases is increasing, especially after pandemic of COVID-19. The oldest and the most approved theory which explains mechanism of depression’s development is a monoamine hypothesis. Effectiveness of most antidepressant drugs based on this theory. It assumes that the typical symptoms of depression are results of changed concentration of monoamines or incorrect monoaminergic transmission. The aim of this article is to present drugs which have influence on level of biogenic amines and are used in treatment of depressive disorders. Some of those drugs are the first choice in cure of this disease. In spite of adverse effects and often delayed onset of action of pharmacotherapy, it is still the first line in treatment of depression.
抑郁症是当前最严重的精神疾病之一。抑郁症可能影响到每个人,它会导致社会功能障碍,并可能导致自杀死亡。抑郁症是一个严重的问题,因为其病例数量正在增加,特别是在COVID-19大流行之后。最古老和最被认可的解释抑郁症发展机制的理论是单胺假说。大多数抗抑郁药物的有效性基于这一理论。它假定抑郁症的典型症状是单胺浓度变化或不正确的单胺能传递的结果。本文的目的是介绍影响生物胺水平的药物,并用于治疗抑郁症。其中一些药物是治疗这种疾病的首选药物。尽管药物治疗有副作用,而且常常延迟起效,但它仍然是治疗抑郁症的第一线药物。
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引用次数: 0
Medicinal plants: A promising source of anti-diabetic agents in sub-Sahara Africa 药用植物:撒哈拉以南非洲抗糖尿病药物的一个有前途的来源
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0012
C. Aloke, C. Egwu, Oluwasola Abayomi Adelusi, Nnamdi Chinaka, S. Kanu, Peace Nzubuchukwu Ogbodo, B. Akumadu, Ikechukwu Achilonu
Abstract The rising burden of Diabetes mellitus (DM) globally and particularly in sub-Sahara Africa calls for alternative treatment solutions. This is because the currently available drugs for its management are limited due to undesirable adverse effects and high cost. Thus, this review explores diabetes and summarizes its treatment options, focusing mainly on medicinal plants therapy. Information on twenty-five selected medicinal plants from sub-Sahara Africa having hypoglycemic and anti-diabetic potentials was obtained via electronic search of major databases, such as Pubmed/Medline, Scopus, Google Scholar and web of science. Predominant bioactive compounds found in these plants include tannins, carpaine, terpenoids, hexadecenoic acid, luteolin, saponins, glycosides, rutin, quercetin, vindoline and kaempferol. Robust evidence indicates that these medicinal plants and their bioactive components exert their antidiabetic potentials via different mechanisms, including: regeneration of pancreatic β-cell and insulin secretion; inhibition of α-amylase, inhibition of intestinal glucose absorption and liver glucose production; antioxidative stress; limitation of glycogen degradation and gluconeogenesis; anti-inflammatory, immunoregulatory. DM imposes a tremendous burden in the region, and its prevalence is not abating; thus the rich flora of the region with known hypoglycemic and antidiabetic efficacy could be explored as a complementary therapy in its management.
摘要全球范围内,特别是撒哈拉以南非洲地区,糖尿病(DM)负担不断增加,需要替代治疗方案。这是因为目前可用于其管理的药物由于不良反应和高成本而受到限制。因此,这篇综述探讨了糖尿病并总结了其治疗方案,主要集中在药用植物治疗上。通过电子搜索主要数据库,如Pubmed/Medline、Scopus、Google Scholar和科学网,获得了来自撒哈拉以南非洲的25种具有降血糖和抗糖尿病潜力的药用植物的信息。在这些植物中发现的主要生物活性化合物包括单宁、甜菜碱、萜类、十六碳烯酸、木犀草素、皂苷、糖苷、芦丁、槲皮素、长春花碱和山奈酚。有力的证据表明,这些药用植物及其生物活性成分通过不同的机制发挥其抗糖尿病潜力,包括:胰腺β细胞的再生和胰岛素分泌;抑制α-淀粉酶,抑制肠道葡萄糖吸收和肝脏葡萄糖生成;抗氧化应激;糖原降解和糖异生的限制;抗炎、免疫调节。糖尿病在该地区造成了巨大的负担,其流行率并没有下降;因此,该地区丰富的植物群具有已知的降血糖和抗糖尿病功效,可以作为其管理的补充疗法进行探索。
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引用次数: 1
Adiponectin as a novel predictive biomarker of multiple sclerosis course 脂联素作为一种新的预测多发性硬化过程的生物标志物
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0017
J. Gałązka, A. Polak, B. Matyjaszek-Matuszek
Abstract Multiple sclerosis (MS) is a serious neurological disease, the actual worldwide prevalence of which is estimated to be 2,8 million people (35,9 per 100,000). During the course of MS, various neurological symptoms and its complications result in raising patient disability, which range from skeletal muscles impairment, to losses in cognitive functions. Achieving control over course of MS progression appears to be crucial in its treatment. This enforces the need for recognizing novel predictive factors so as to allow prognosis of future remissions and/or progressions. Adiponectin, hormone secreted by adipose tissue, currently is considered as a possible candidate for such a biomarker. The aim of this review is to summarise present knowledge and to assess possible clinical usage. According to collected data, adiponectin measurements in serum and cerebrospinal fluid appear to provide plausible and useful biomarkers in predicting the course of MS. Further studies are, however, needed, especially using non-invasive, but promising sources such as saliva.
摘要多发性硬化症(MS)是一种严重的神经系统疾病,全球实际患病率估计为280万人(每100000人中有35,9人)。在多发性硬化症的过程中,各种神经系统症状及其并发症会导致患者残疾,从骨骼肌损伤到认知功能丧失。实现对多发性硬化症进展过程的控制似乎对其治疗至关重要。这加强了识别新的预测因素的必要性,以便对未来的缓解和/或进展进行预测。脂联素是脂肪组织分泌的激素,目前被认为是这种生物标志物的可能候选者。本综述的目的是总结现有知识并评估可能的临床应用。根据收集的数据,血清和脑脊液中的脂联素测量似乎为预测多发性硬化症的病程提供了可信和有用的生物标志物。然而,还需要进一步的研究,特别是使用非侵入性但有前景的来源,如唾液。
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引用次数: 0
Determination of some drugs used against neurodegenerative disorders by micellar electrokinetic chromatography with running buffer containing SDS SDS缓冲液胶束电动色谱法测定某些神经退行性疾病药物
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0021
Adam Traczuk, Kamila Jaglinska, Beata Polak
Abstract In this work, analysis of some drugs used in the treatment of neurodegenerative disorders (sulpiride, olanzapine, carbamazepine, trazodone, clomipramine, and pridinol) was achieved through micellar electrokinetic chromatography (MEKC). The effect of surfactant (sodium dodecylsulphate), acetonitrile, and buffer pH and concentration on the solute retention was also investigated. Successful separation of all compound mixtures was obtained. The method was applied for the quantitative analysis of investigated compounds, and the LOD and LOQ were determined. The LOD values were in the range from 0.0127 mg/mL for clomipramine, to 0.1398 mg/mL for pridinol, while LOQ were in the range 0.0384 mg/mL for clomipramine, to 0.4237 for pridinol. The mode was also applied for the determination of investigated solutes in pharmaceutical prescriptions.
摘要在本工作中,通过胶束电动色谱法(MEKC)对一些用于治疗神经退行性疾病的药物(舒必利、奥氮平、卡马西平、曲唑酮、克罗米帕明和丙二醇)进行了分析。还研究了表面活性剂(十二烷基硫酸钠)、乙腈、缓冲液pH和浓度对溶质保留的影响。成功地分离了所有化合物混合物。将该方法应用于所研究化合物的定量分析,并测定了LOD和LOQ。氯米帕明的LOD值在0.0127 mg/mL至0.1398 mg/mL的范围内,而氯米帕敏的LOQ值在0.0384 mg/mL至0.4237的范围内。该模式也适用于药物处方中所研究溶质的测定。
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引用次数: 0
Development and validation of a new bioanalytical method for quantification of CDK4/6 inhibitor in Spiked Human Plasma by HPLC-UV HPLC-UV定量人血浆中CDK4/6抑制剂的新方法的建立与验证
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0014
Rakesh U. Shelke, Dinesh D. Rishipathak
Abstract A sensitive and accurate high performance liquid chromatography method utilizing ultraviolet/visible light detection (HPLC-UV) for the quantification of Ribociclib in Spiked Human Plasma by HPLC-UV was developed and validated. Ribociclib (RCB) and the internal standard (IS), Trifluridine, were first extracted from plasma samples by a simple Protein Precipitation extraction using Acetonitrile. Plasma concentration of RCB and internal standard were then analyzed by applying reversed phase chromatography using Orochem orosil C18 (4.6 mm × 250 mm, 5 μ) and elution with a isocratic mobile phase consisting of 10 mM phosphate buffer – Acetonitrile (60:40, v/v) adjusted to pH 3.0 at a flow rate of 1.0 ml/min. Detection of RCB and the IS was subsequently done at a wavelength of 260 nm. The limit of quantification was 10 ng/ml. The calibration curve was linear (R2>0.998) over the concentration range of 10-1000 ng/ml. For human plasma, the accuracy and precision were within ±15% and ≤15%, respectively, for all concentrations, except for the lower limit of quantification, where they were within ≤20%.
摘要:建立了一种高效液相色谱紫外/可见光检测(HPLC-UV)定量加标人血浆中核糖西尼(Ribociclib)的方法。首先用乙腈进行简单的蛋白沉淀萃取,从血浆样品中提取核糖环尼(RCB)和内标物Trifluridine。采用Orochem orosil C18 (4.6 mm × 250 mm, 5 μ)反相色谱法分析血浆中RCB和内标物的浓度,以10 mm磷酸盐缓冲液-乙腈(60:40,v/v)为等温流动相,流速为1.0 ml/min,洗脱至pH 3.0。随后在260 nm波长下对RCB和IS进行检测。定量限为10 ng/ml。在10 ~ 1000 ng/ml的浓度范围内,校准曲线呈线性(R2>0.998)。对于人血浆,除定量下限在≤20%以内外,所有浓度的准确度和精密度分别在±15%和≤15%以内。
{"title":"Development and validation of a new bioanalytical method for quantification of CDK4/6 inhibitor in Spiked Human Plasma by HPLC-UV","authors":"Rakesh U. Shelke, Dinesh D. Rishipathak","doi":"10.2478/cipms-2023-0014","DOIUrl":"https://doi.org/10.2478/cipms-2023-0014","url":null,"abstract":"Abstract A sensitive and accurate high performance liquid chromatography method utilizing ultraviolet/visible light detection (HPLC-UV) for the quantification of Ribociclib in Spiked Human Plasma by HPLC-UV was developed and validated. Ribociclib (RCB) and the internal standard (IS), Trifluridine, were first extracted from plasma samples by a simple Protein Precipitation extraction using Acetonitrile. Plasma concentration of RCB and internal standard were then analyzed by applying reversed phase chromatography using Orochem orosil C18 (4.6 mm × 250 mm, 5 μ) and elution with a isocratic mobile phase consisting of 10 mM phosphate buffer – Acetonitrile (60:40, v/v) adjusted to pH 3.0 at a flow rate of 1.0 ml/min. Detection of RCB and the IS was subsequently done at a wavelength of 260 nm. The limit of quantification was 10 ng/ml. The calibration curve was linear (R2>0.998) over the concentration range of 10-1000 ng/ml. For human plasma, the accuracy and precision were within ±15% and ≤15%, respectively, for all concentrations, except for the lower limit of quantification, where they were within ≤20%.","PeriodicalId":11071,"journal":{"name":"Current Issues in Pharmacy and Medical Sciences","volume":"36 1","pages":"81 - 86"},"PeriodicalIF":0.3,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46619730","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
The role of the L-arginine-NO-cGMP pathway in the development of tolerance to mephedrone-induced hyperlocomotion in mice l -精氨酸- no - cgmp通路在甲氧麻黄酮诱导小鼠过度运动耐受发展中的作用
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0020
Gabriela Bielecka-Papierz, E. Poleszak, A. Szopa, J. Listos, Jolanta Orzelska-Górka, Małgorzata Jakóbczuk, Kamila Baluk, S. Talarek, A. Serefko
Abstract The tendency of a psychostimulant to increase locomotion in rodents is considered to be associated with its addictive properties. Mephedrone, one of the most popular psychoactive substances used recreationally, is known to enhance locomotor activity in mice, but little is known about the potential development of tolerance to its central effects. In the present study, we decided to evaluate the possible involvement of the L-arginine-NO-cGMP pathway in the development of tolerance to mephedrone-induced hyperlocomotion. Experiments were performed on adult male Albino Swiss mice, and the locomotor activity was measured automatically. Our work indicated that a 5-day administration of L-NAME (25 or 50 mg/kg/day), methylene blue (5 or 10 mg/kg/day), and L-arginine hydrochloride (i.e., 250 mg/kg/day) prevented the development of tolerance to mephedrone-induced (5 mg/kg/day) hyperlocomotion, whereas treatment with L-arginine hydrochloride at a dose of 125 mg/kg/day potentiated the development of tolerance to this central effect of mephedrone. Summarizing, our data revealed that the L-arginine-NO-cGMP pathway contributes to the development of tolerance to mephedrone’s central effects since inhibition of this signalling via blocking of NOS or NO-stimulated sGC prevented the development of tolerance to mephedrone-induced hyperlocomotion. As for cGMP-regulated phosphodiesterases, most probably they are not involved in these mechanisms.
摘要精神刺激剂增加啮齿类动物运动能力的趋势被认为与其成瘾性有关。甲基苯丙胺是娱乐性使用的最受欢迎的精神活性物质之一,已知可增强小鼠的运动活性,但对其中枢作用耐受性的潜在发展知之甚少。在本研究中,我们决定评估L-精氨酸-NO-cGMP途径在对甲氧麻黄酮诱导的高运动耐受性发展中的可能参与。在成年雄性Albino Swiss小鼠上进行实验,并自动测量运动活性。我们的研究表明,L-NAME(25或50 mg/kg/天)、亚甲蓝(5或10 mg/kg/天,而以125mg/kg/天的剂量用L-精氨酸盐酸盐治疗增强了对甲氧麻黄酮的这种中心作用的耐受性的发展。总之,我们的数据表明,L-精氨酸-NO-cGMP途径有助于对甲氧麻黄酮的中心作用产生耐受性,因为通过阻断NOS或NO刺激的sGC来抑制这种信号传导,阻止了对甲氧甲黄酮诱导的高运动产生耐受性。至于cGMP调节的磷酸二酯酶,它们很可能与这些机制无关。
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引用次数: 1
Penicillin-binding protein genotyping of penicillin-nonsusceptible Streptococcus pneumoniae isolates from the nasopharynx of healthy preschool children 健康学龄前儿童鼻咽非青霉素敏感肺炎链球菌青霉素结合蛋白基因分型研究
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0016
Karolina Kielbik, Adrian Bakiera, I. Korona-Głowniak
Abstract Streptococcus pneumoniae is one of the most frequent bacterial identified causes of community-acquired pneumonia, otitis media and meningitis. It is, as well, a common cause of bacteraemia’s significant morbidity and mortality. Beta-lactam antibiotics (BLAs) are the first line of empirical treatment for pneumococcal infections. The targets of BLAs are penicillin-binding proteins (PBPs), the modifications of which are one of the reasons why pneumococci are non-susceptible to BLAs. In our work, a total of 39 Streptococcus pneumoniae isolates were obtained from 176 healthy children, both vaccinated and non-vaccinated. The isolates were tested for antimicrobial susceptibility, and their penicillin-binding proteins (PBPs) were typed by the restriction fragment length of the polymorphism analysis of their pbp genes. The most frequent serotypes among the penicillin non-susceptible Streptococcus pneumoniae (PNSSP) isolates were 23B, 35B and 19F. Restriction enzyme analyses of pbp1a, pbp2b, and pbp2x genes revealed 5, 3 and 3 different patterns, respectively, and a total of 4 different PBPs profiles of PNSSP isolates belonging to serotypes not included in pneumococcal conjugate vaccines were demonstrated. We conclude that the level of resistance should be monitored constantly to ascertain the effect of current pneumococcal conjugate vaccines, as well as to recognize new circumstances developing in Poland, as well as the possibility of multiple, independent imports of resistant strains from abroad.
摘要肺炎链球菌是引起社区获得性肺炎、中耳炎和脑膜炎的最常见细菌之一。它也是引起菌血症发病率和死亡率增高的常见原因。β -内酰胺类抗生素(BLAs)是肺炎球菌感染的第一线经验性治疗。bla的靶标是青霉素结合蛋白(pbp),其修饰是肺炎球菌对bla不敏感的原因之一。在我们的工作中,从176名健康儿童(包括接种疫苗和未接种疫苗的儿童)中共分离出39株肺炎链球菌。对分离菌株进行了药敏试验,并通过pbp基因的限制性内切片段长度多态性分析对其青霉素结合蛋白(pbp)进行了分型。青霉素不敏感肺炎链球菌(PNSSP)分离株中最常见的血清型为23B、35B和19F。pbp1a、pbp2b和pbp2x基因的限制性内切酶分析分别显示出5种、3种和3种不同的模式,属于肺炎球菌结合疫苗不包括的血清型的PNSSP分离株共有4种不同的PBPs谱。我们的结论是,应不断监测耐药性水平,以确定当前肺炎球菌结合疫苗的效果,并认识到波兰出现的新情况,以及从国外独立进口多种耐药菌株的可能性。
{"title":"Penicillin-binding protein genotyping of penicillin-nonsusceptible Streptococcus pneumoniae isolates from the nasopharynx of healthy preschool children","authors":"Karolina Kielbik, Adrian Bakiera, I. Korona-Głowniak","doi":"10.2478/cipms-2023-0016","DOIUrl":"https://doi.org/10.2478/cipms-2023-0016","url":null,"abstract":"Abstract Streptococcus pneumoniae is one of the most frequent bacterial identified causes of community-acquired pneumonia, otitis media and meningitis. It is, as well, a common cause of bacteraemia’s significant morbidity and mortality. Beta-lactam antibiotics (BLAs) are the first line of empirical treatment for pneumococcal infections. The targets of BLAs are penicillin-binding proteins (PBPs), the modifications of which are one of the reasons why pneumococci are non-susceptible to BLAs. In our work, a total of 39 Streptococcus pneumoniae isolates were obtained from 176 healthy children, both vaccinated and non-vaccinated. The isolates were tested for antimicrobial susceptibility, and their penicillin-binding proteins (PBPs) were typed by the restriction fragment length of the polymorphism analysis of their pbp genes. The most frequent serotypes among the penicillin non-susceptible Streptococcus pneumoniae (PNSSP) isolates were 23B, 35B and 19F. Restriction enzyme analyses of pbp1a, pbp2b, and pbp2x genes revealed 5, 3 and 3 different patterns, respectively, and a total of 4 different PBPs profiles of PNSSP isolates belonging to serotypes not included in pneumococcal conjugate vaccines were demonstrated. We conclude that the level of resistance should be monitored constantly to ascertain the effect of current pneumococcal conjugate vaccines, as well as to recognize new circumstances developing in Poland, as well as the possibility of multiple, independent imports of resistant strains from abroad.","PeriodicalId":11071,"journal":{"name":"Current Issues in Pharmacy and Medical Sciences","volume":"36 1","pages":"94 - 98"},"PeriodicalIF":0.3,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45285603","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Healthcare professional’s knowledge and awareness of the medication error reporting systems in the Kuwaiti hospitals 医疗保健专业人员对科威特医院药物错误报告系统的了解和认识
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-01 DOI: 10.2478/cipms-2023-0015
Mohammad Saada
Abstract Objective. A survey was conducted to explore healthcare professional’s (HCPs) knowledge and attitude towards medication errors reporting processes and systems used in their local hospitals. Methods. There were 696 respondents and the observational survey showed the diverse perspectives of HCPs from diverse professions (doctors, pharmacists and nurses) who are at different stages in their career. The survey results highlighted the deficiencies in the medication safety management process, including the follow-up on witnessed or discovered medication errors, the effectiveness of the used reporting systems for medication errors, the standardisation of electronic prescribing software, and the training of HCPs at the six hospitals on medication safety. Key finding. Only 46% of the surveyed stated that their hospital had a mechanism in place for reporting medication errors and 60.7% of the participants agreed that they would submit reports provided the system is not used for performance management and only those need to know will be able to identify their name. Regarding prescription writing, 51% of surveyed HCPs said they utilise electronic prescribing software; however, the overall usage rate of electronic prescribing systems was 49%, with handwritten prescriptions remaining the option used in the majority of the time. In terms of HCP training, 20% of the survey respondents said they did not receive any instruction or direction in the hospitals on pharmacovigilance and patient safety. Conclusions. The Kuwaiti MoH should build a national electronic incident reporting system and establish standardised rules and protocols for incident reporting that is to be anonymous and of compulsory use by all government and private hospitals.
摘要目标。进行了一项调查,以探讨医疗保健专业人员(HCP)对当地医院使用的药物错误报告流程和系统的知识和态度。方法。共有696名受访者,观察性调查显示了来自不同职业(医生、药剂师和护士)的HCP的不同观点,他们正处于职业生涯的不同阶段。调查结果强调了药物安全管理过程中的不足,包括对目击或发现的药物错误的跟踪、使用的药物错误报告系统的有效性、电子处方软件的标准化,以及六家医院HCP的药物安全培训。关键发现。只有46%的受访者表示,他们的医院有报告药物错误的机制,60.7%的参与者同意,如果该系统不用于绩效管理,他们将提交报告,只有那些需要知道的人才能识别自己的姓名。关于处方书写,51%的受访HCP表示他们使用电子处方软件;然而,电子处方系统的总体使用率为49%,手写处方在大多数情况下仍然是使用的选项。在HCP培训方面,20%的受访者表示,他们在医院没有收到任何关于药物警戒和患者安全的指导或指示。结论。科威特卫生部应建立一个国家电子事故报告系统,并为事故报告制定标准化规则和协议,这些规则和协议应是匿名的,所有政府和私立医院都必须使用。
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引用次数: 0
Mephedrone – a synthetic derivative of cathinone 甲氧麻黄酮-卡西酮的合成衍生物
IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-03-01 DOI: 10.2478/cipms-2023-0011
Gabriela Bielecka-Papierz, E. Poleszak, Anna Serafko
Abstract Novel psychoactive substances (NPS) are a very diverse group of recreational drugs that mimic effects of classic drugs of abuse and, at least at the beginning, are not usually prohibited. Representative of this group is mephedrone – a cathinone derivative. It is widely used as a recreational drug, particularly among club guests. Mephedrone`s effects are compared to effects of cocaine and MDMA but are more short-lived and include: psychostimulation, enhanced empathy, reduced feeling of tiredness, euphoria, hallucinations. This drug also exerts adverse effects, such as: anxiety, delusions, paranoia, psychosis, increased body temperature, elevated blood pressure, sleep disturbances. According to surveys performed on mephedrone users, it may be addictive. Those findings confirms a growing number of behavioural and molecular studies on animals. Mephedrone acts mainly via increasing monoamine transmission through increasing release of dopamine, serotonin and noradrenaline into synaptic cleft, inhibiting their re-uptake and reducing their metabolism. However, participation of other transmitters, modulators and pathways are investigated, including glutamate and nitric oxide. Favorable routes of administering mephedrone is intranasal and per os. Moreover, most often drug users use it in a binge way, e.g. taking repeated doses of a drug in a short period of time. According to animal studies, this pattern of mephedrone use leaves more neural injuries than taking it regularly, but in smaller doses. Our aim was to present a short, but essential, overview of the current knowledge on mephedrone, focusing on its effects, mechanism of action, animal studies evaluating its influence on the brain structures, toxicity and pharmacokinetics.
新型精神活性物质(NPS)是一类非常多样化的娱乐性药物,它们模仿经典药物的滥用效果,至少在开始时通常不被禁止。这类药物的代表是甲氧麻黄酮——卡西酮的衍生物。它被广泛用作消遣性毒品,尤其是在俱乐部客人中。与可卡因和MDMA相比,甲氧麻黄酮的效果更短暂,包括:精神刺激、增强同理心、减少疲惫感、欣快感和幻觉。这种药物也有副作用,如:焦虑、妄想、偏执、精神病、体温升高、血压升高、睡眠障碍。根据对甲氧麻黄酮使用者的调查,它可能会上瘾。这些发现证实了越来越多的动物行为和分子研究。甲氧麻黄酮主要通过增加多巴胺、血清素和去甲肾上腺素向突触间隙的释放增加单胺的传递,抑制它们的再摄取,降低它们的代谢。然而,其他递质、调节剂和途径的参与也被研究,包括谷氨酸和一氧化氮。给予甲氧麻黄酮的有利途径是鼻内和静脉注射。此外,大多数情况下,吸毒者以暴饮暴食的方式使用它,例如在短时间内重复服用一种药物。根据动物研究,这种使用甲氧麻黄酮的模式比定期服用更容易造成神经损伤,但剂量较小。我们的目的是对甲氧麻黄酮的现有知识进行简短但必要的概述,重点是其作用、作用机制、评估其对大脑结构影响的动物研究、毒性和药代动力学。
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引用次数: 0
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