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P53?A review of the use of intravenous immunoglobulin (IVIG) in paediatric neurology patients at a children’s hospital from April 2017 to April 2019

机译:P53?从2017年4月到2019年4月,儿童医院对儿童医院静脉内免疫球蛋白(IVIG)在儿童医院使用的述评

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Aim To determine if the use of IVIG in neurology patients at a children’s hospital was appropriate according to local 1 and national guidance 2 3 . Method All paediatric neurology patients supplied with IVIG from the hospital pharmacy from April 2017 to April 2019 were identified retrospectively using the pharmacy dispensing system. The standards were based on local and national guidelines from the Department of Health (DoH). Patients’ details, for example indication and dose, were recorded and analysed on Microsoft Excel. Standards 100% of patients will have an IVIG request form completed. 100% of patients will have IVIG prescribed for indications approved by the DoH. 100% of patients will have panel approval before being supplied with IVIG. 100% of patients will have the appropriate dose and duration of IVIG for the corresponding indication according to guidelines. Results A total of 20 patients were identified for this audit with 4 patients from 2017/18 and 16 from 2018/19. Standard 1 was met by 100% of patients. 8 patients (40%) were given IVIG for indications that do not have automatic approval from the DoH guidelines, i.e. for indications under ‘grey’ or ‘black’ categories. 2 patients (10%) did not have panel approval and both of these patients had acute flaccid myelitis, which is a ‘black’ indication. 16 (80%) patients were prescribed IVIG at a dose or duration advised by local and DoH guidelines. Conclusion and Discussion During the study period the method for completing the IVIG request forms changed to a new electronic system. The two patients with acute flaccid myelitis were incorrectly approved by the IVIG panel due to an error in the new electronic request form. The approval system was updated to prevent this error from reoccurring. All other patients that did not have automatic approval from the DoH guideline were approved by the local IVIG panel before use. Overall cost and usage increased significantly from 2017/18 to 2018/19; approximately £9,300 and £57,000 respectively. One patient was given a higher dose over a shorter period but the total dose for each course was the same. The shortened regimen meant that doses were rounded to the nearest vial size, which reduced wastage. The demand for IVIG is increasing and due to its limited availability and high cost, it is important that IVIG is only given to patients that meet the specified requirements. Recommendations Ensure patients are only supplied with IVIG if the above standards are met Neurology pharmacist to re-audit data annually to ensure that IVIG is being given according to guidelines.
机译:目的是根据当地1和国家指导2 3确定儿童医院神经内科患者的IVIG是否适合。方法从2017年4月到2019年4月到2019年4月的医院药房供应的所有儿科神经科患者的回顾性地使用药房分配系统。标准基于卫生部(DOH)的本地和国家指南。在Microsoft Excel上记录和分析患者的细节,例如指示和剂量,并分析。标准100%的患者将完成IVIG申请表。 100%的患者将有IVIG规定的ovig被福伊批准的迹象。在随IVIG提供之前,100%的患者将有小组批准。 100%的患者将具有适当剂量和持续时间的IVIG,用于根据指导方针进行相应的指示。结果共有20名患者为本审计,2017/1911年的4名患者有4名患者。通过100%的患者满足标准1。 8名患者(40%)给予IVIG,迹象表明没有从DOH指南那里自动批准,即“灰色”或“黑色”类别下的适应症。 2名患者(10%)没有面板批准,这些患者两者都有急性弛缓性骨髓炎,这是一个“黑色”指示。 16(80%)患者在局部和DOH指南提出的剂量或持续时间进行规定的IVIG。结论与讨论在研究期间,完成IVIG申请表格的方法改为新的电子系统。由于新电子请求表格中的错误,这两名急性皮脂骨髓炎患者因IVIG面板错误地批准。更新批准系统以防止此错误重新核销。所有其他没有从DOH指南自动批准的患者在使用前通过本地IVIG面板批准。总成本和使用率从2017/18到2018/19显着增加;大约9,300英镑和57,000英镑。一名患者在较短的时间内给出更高的剂量,但每种过程的总剂量相同。缩短的方案意味着剂量被圆形到最接近的小瓶尺寸,这减少了浪费。对IVIG的需求正在增加,并且由于其可用性和高成本有限,因此只有符合规定要求的患者才能提供IVIG。建议确保患者只有IVIG提供,如果上述标准符合神经内科医师每年重新审核数据,以确保根据指南给出IVIG。

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