[Off-label use of intravenous immunoglobulin g in a highly complex pediatric hospital in Argentina. A prospective observational study]

Roxana Rivero, Ingrid Strusberg, Silvia Joekes, Silvana Yori, Carolina Barros Herrero, Marcela Noemí Rousseau, Daniela Fontana
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Abstract

Introduction: The World Health Organization recommends prioritizing safe and effective drugs proven by clinical or epidemiological studies. However, in population groups with little research, a drug can be used for an indication or pharmaceutical form different from that approved by the regulatory agency (off-label), extrapolating data from studies in adults and exposing pediatric patients. to develop an Adverse Drug Reaction (ADR) due to safety considerations that have not been systematically studied. Intravenous immunoglobulin (IVIg), a high-cost drug, is used with scant evidence in some low-prevalence pathologies. This paper describes and analyzes the off-label use of IVIg at the J. P. Garrahan Pediatric Hospital.

Methods: Observational, descriptive, prospective study on off-label indications of IVIg. The sampling technique was non-probabilistic and for convenience during 7 months.

Results: 305 IVIg infusions were studied, corresponding to 111 patients. The indication classification showed that 22% (n=67) of the infusions were off-label. In neurology there was a higher percentage of off-label indications (46%) and within them 45% corresponded to the use in neurological disorders. 81% of the doses indicated off-label were in the range 0.8-1g/kg. The off-label infusions presented 61.5% (n=8) of the ADRs. Those from the Neurology service represented 87.5%; 75% being from the "Neurological disorders" group.

Conclusion: In some cases, IVIg was indicated in an off-label manner, finding a statistically significant relationship with the appearance of ADR. This finding motivates the proposition of new hypotheses to carry out more studies.

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[阿根廷一家高度复杂的儿科医院在标签外使用静脉注射免疫球蛋白 g。前瞻性观察研究]
导言:世界卫生组织建议优先使用经临床或流行病学研究证实安全有效的药物。然而,在研究较少的人群中,药物的适应症或剂型可能不同于监管机构批准的适应症或剂型(标签外),从成人研究中推断出的数据可能会使儿科患者发生药物不良反应(ADR)。静脉注射免疫球蛋白(IVIg)是一种高成本药物,用于某些低发病率病症的证据不足。本文描述并分析了 J. P. Garrahan 儿科医院在标签外使用 IVIg 的情况:方法:对IVIg标签外适应症的观察性、描述性、前瞻性研究。抽样技术为非概率性和方便抽样,为期 7 个月:研究共对 111 名患者进行了 305 次静脉注射。适应症分类显示,22%(n=67)的输液属于标签外适应症。在神经内科,标签外适应症的比例较高(46%),其中45%用于神经系统疾病。81%的标示外剂量在 0.8-1g/kg 之间。61.5%(n=8)的不良反应发生在标签外输液。来自神经内科的不良反应占87.5%,其中75%来自 "神经系统疾病 "组:结论:在某些病例中,IVIg 是以标签外的方式使用的,这与出现 ADR 有显著的统计学关系。这一发现促使人们提出新的假设,以开展更多的研究。
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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
60
审稿时长
20 weeks
期刊介绍: The Journal of the Faculty of Medical Sciences is a scientific publication of the Secretariat of Science and Technology of the Faculty of Medical Sciences of the National University of Cordoba. Its objective is to disseminate and promote research work related to Medical and Biological Sciences. It publishes scientific works of national and international professionals on different topics related to health sciences from the field of medicine, nursing, kinesiology, diagnostic imaging, phonoaudiology, nutrition, public health, chemical sciences, dentistry and related.
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