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Paediatric and perinatal drug therapy最新文献

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Is Pharmacy Dispensing Information Useful to Identify Problems with Analgesic Prescribing in Children 药房配药信息对识别儿童止痛药处方问题有用吗
Pub Date : 2003-06-01 DOI: 10.1185/146300903322012068
Y. Velázquez-Armenta, A. Nava-Ocampo
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引用次数: 4
A European clinical trials registry for children 欧洲儿童临床试验登记处
Pub Date : 2003-01-01 DOI: 10.1185/146300903322012004
C. Pandolfini, M. Bonati, H. Sammons, I. Choonara, É. Jacqz-Aigrain, I. Danés, I. Fuentes, J. Arnau
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引用次数: 5
The Use of Sodium Benzoate in a Ten-fold Overdose of Asparaginase 苯甲酸钠治疗天冬酰胺酶10倍过量
Pub Date : 2002-10-01 DOI: 10.1185/146300902322125839
A. Doloy, S. Roy, S. Djoussa-Kambou, F. Legrand, F. Brion, A. Rieutord
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引用次数: 3
Antibiotics and Acute Renal Failure in Children with Cystic Fibrosis 囊性纤维化儿童的抗生素和急性肾功能衰竭
Pub Date : 2002-10-01 DOI: 10.1185/146300902322125910
J. Drew, A. Watson, J. Evans, A. Smyth
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引用次数: 16
From Medication Errors to Safe Medication Practice 从用药错误到安全用药实践
Pub Date : 2002-10-01 DOI: 10.1185/146300902322125884
Tony Nunn
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引用次数: 0
Approaches to Studying the Development of Drug Metabolism in Children 儿童药物代谢发展的研究方法
Pub Date : 2002-10-01 DOI: 10.1185/146300902322125866
T. Johnson
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引用次数: 0
Medication Errors in Children - an Eight Year Review Using Press Reports 儿童用药错误——八年新闻报道回顾
Pub Date : 2002-10-01 DOI: 10.1185/146300902322125893
D. Cousins, A. Clarkson, S. Conroy, I. Choonara
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引用次数: 40
Drug Toxicity and Adverse Drug Reactions in Children - A Brief Historical Review 儿童的药物毒性和药物不良反应-简要的历史回顾
Pub Date : 2002-05-01 DOI: 10.1185/146300902322125109
I. Choonara, M. Rieder
AbstractDrug toxicity in association with adverse drug reactions is common in hospitalisedchildren. The toxicity of medicines in children is different to that seen in adults.There are also differences between different age groups of paediatric patientswith neonates being generally at greater risk for experiencing a drug-associatedadverse event. The major examples of drug toxicity that have occurred inpaediatric patients are reviewed ranging from percutaneous toxicity over 100years ago to formulation errors and toxicity associated with normal,developmental alterations in drug metabolism . The need to learn from previouscases of drug toxicity to prevent future cases is paramount. Paed Perinatal Drug Ther 2002; 5: 12– 18 Key words: Drug toxicity – drug metabolism – children Introduction Adverse drug reactions ( ADRs ) are commonclinical problems in both paediatric and adultmedicine. Over 9% of hospitalised children haveadverse reactions to therapy and up to 4% of allhospital admissions are the consequence of ADRs
摘要药物毒性合并药物不良反应在住院儿童中很常见。药物对儿童的毒性与对成人的毒性不同。不同年龄组的儿科患者之间也存在差异,新生儿通常面临更大的药物相关不良事件风险。本文回顾了发生在儿科患者身上的药物毒性的主要例子,从100多年前的经皮毒性到配方错误和与药物代谢正常发育改变相关的毒性。从以前的药物毒性病例中学习以预防未来的病例是至关重要的。围产期用药指南2002;[05:12 - 18]关键词:药物毒性药物代谢儿童导论药物不良反应(adr)是儿科和成人医学中常见的临床问题。超过9%的住院儿童对治疗有不良反应,高达4%的住院儿童是adr的后果
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引用次数: 51
Neuromuscular Blocking Agents in Critically Ill Children 危重儿童的神经肌肉阻滞剂
Pub Date : 2002-05-01 DOI: 10.1185/146300902322125145
S. Playfor
Neuromuscular blockade is used in critically ill children for a variety of reasons. The physiology and pharmacology of neuromuscular blocking agents is reviewed. The effect of hypothermia on the pharmacodynamics of neuromuscular blockade is discussed. The ideal agent would have a rapid rate of onset with spontaneous reversal after discontinuation. Patients receiving neuromuscular blocking agents need to be assessed for the degree of blockade that is being sustained. The need to temporarily discontinue infusions of neuromuscular blocking agents to enable an assessment of the level of sedation or to allow an assessment of neuromuscular function is highlighted. Paed Perinatal Drug Ther 2002; 5: 35–46
由于各种原因,神经肌肉阻滞用于危重儿童。综述了神经肌肉阻滞剂的生理和药理作用。讨论了低温对神经肌肉阻断药药效学的影响。理想的药物起效快,停药后可自行逆转。接受神经肌肉阻滞剂治疗的患者需要评估其持续的阻断程度。需要暂时停止输注神经肌肉阻断剂,以评估镇静水平或允许评估神经肌肉功能。围产期用药指南2002;5: 35-46
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引用次数: 1
Adverse Drug Reactions to Off-label Drugs on a Paediatric Ward: an Italian Prospective Pilot Study 儿科病房对超说明书药物的不良反应:意大利前瞻性试点研究
Pub Date : 2002-05-01 DOI: 10.1185/146300902322125118
P. Impicciatore, A. Mohn, F. Chiarelli, C. Pandolfini, M. Bonati
Recently published studies examining the extent of off-label drug prescribing in various European paediatric wards have reported that off-label use is widespread and particularly high in Italy. So far, however, no studies have investigated the extent to which adverse drug reactions (ADRs) due to off-label drug use occur in Italy. To evaluate the risk associated with off-label drug use in paediatric inpatients, a prospective surveillance study was carried out in the paediatric ward of a teaching hospital over a 9 month period. Forty-one children (mean age: 7.2 years, 58% male ), out of a study population of 1619 patients, experienced ADRs. In 29 children the ADRs were due to in hospital drug therapies, while in 12 they were due to medicines administered in the community. Urticaria (11 cases), vomiting and rash (5 cases each ) and tremor (4 cases) were the most common ADRs. Eight ADRs (20%) were classified as severe. The drugs most frequently associated with ADRs were salbutamol (5 cases) and coamoxiclav (4 cases). Off-label drug prescriptions were responsible for 38% of inpatient ADRs and for 42% of the ADRs occurring in the community that led to hospitalisation. The use of drugs not licensed for paediatric use (8 cases) or for indications for which the drug was not licensed (6 cases) were the off-label categories most frequently associated with ADRs. Drugs used for diagnostic tests in endocrinology were responsible for one third of ADRs due to off-label uses. The results of this study suggest a high risk of ADRs associated with offlabel prescribing in children, both in the hospital and in the community. This pilot study also demonstrates the feasibility of an ADR monitoring system that could take into account important issues relating to rational drug prescribing in paediatric patients. In order to achieve a comprehensive risk assessment of off-label drug interventions in children, the study should be continued and expanded to involve the community setting as well.
最近发表的研究调查了欧洲各儿科病房超说明书用药的程度,报告称,超说明书用药很普遍,在意大利尤其严重。然而,到目前为止,还没有研究调查意大利因超说明书用药而发生的药物不良反应(adr)的程度。为了评估儿科住院患者超说明书用药的相关风险,在一家教学医院的儿科病房进行了为期9个月的前瞻性监测研究。在1619例研究人群中,41名儿童(平均年龄:7.2岁,58%为男性)出现了不良反应。在29名儿童中,不良反应是由医院药物治疗引起的,而在12名儿童中,不良反应是由社区给药引起的。最常见的不良反应为荨麻疹(11例)、呕吐、皮疹(各5例)和震颤(4例)。严重不良反应8例(20%)。最常发生不良反应的药物是沙丁胺醇(5例)和复方莫昔拉夫(4例)。说明书外药物处方导致38%的住院不良反应,42%的社区不良反应导致住院。使用未获许可的儿科药物(8例)或药物未获许可的适应症(6例)是最常与adr相关的标签外类别。用于内分泌学诊断测试的药物造成了三分之一的不良反应,这是由于标签外使用造成的。这项研究的结果表明,无论是在医院还是在社区,儿童的超说明书处方都有很高的不良反应风险。这项试点研究还证明了不良反应监测系统的可行性,该系统可以考虑到与儿科患者合理用药有关的重要问题。为了实现对儿童超说明书药物干预的全面风险评估,这项研究应该继续并扩大到社区环境。
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引用次数: 20
期刊
Paediatric and perinatal drug therapy
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