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published in(发表于) 2016/4/10 8:04:38
Jiangsu 26 patients were injected gas problems, some of them blind,

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Jiangsu 26 patients with eye disease is partly blind by gas injection issues _ | | | gas in patients with ophthalmopathy news

Original title: Jiangsu 26 patients surgical medical devices the use of eye damage


Beijing times recently, the Jiangsu Nantong 26 ophthalmopathy patients report that they injected in Nantong University Hospital called perfluorocarbon gas, used in the treatment of conditions such as retinal detachment, but the batch of medical gas belonging to medical devices, after the State food and Drug Administration recalled. At present, the two patients have been blind. Yesterday, the affiliated hospital of Nantong University release reported that this event uses Jing ming, Tianjin new technology development co production with perfluoropropane gas caused the eyes of, apart from the timely redress for victims and follow up review, and take the company to court.


Informed the show Crystal clearly stated the same batch used Tianjin eye use perfluoropropane gas in patients with adverse reactions after a total of 26 officers, took place on June 5, 2015 until June 29. Symptoms of adverse reactions are intraocular fibrinous exudation and lens opacity, atrophy of the optic nerve, retinal vascular occlusion etc. According to the expert opinion of 23 patients with partial overnight salvage operation, remove residual problems gas, fill silicone oil and continued close follow-up and treatment.


Meanwhile, affiliated hospital of Nantong University in communications, said unfortunately for the patients suffering deeply saddened, active remediation and tracking patient review.


Yesterday, Nantong city informed the food and Drug Administration is saying, will closely watch developments, inform the relevant case information will be the first time.


Nantong informed the food and Drug Administration said that the night of July 4, 2015, the affiliated hospital of Nantong University received 7 reports of the adverse event, involving the same product "eye with perfluoropropane gas" in Uveitis patients after reaction may result in permanent damage to body structure, the hospital had to stop using the product and organization to carry out the corresponding treatment. The Council to study the treatment and products used in the city an emergency investigation, sync report to the Center for adverse drug reaction monitoring in Jiangsu Province. The next day, the composition of the Bureau of investigation team went to the hospital to carry out on-site investigations, product qualification, product approval, purchasing procedures, inspection reports, and storage procedures, sales materials such as powers of Attorney conducted a comprehensive investigation, sampling on all of the batch product inventory control, sent to China's food and drug inspection Institute testing.


On July 6, 2015, the agency sent an urgent notice to the city, Tianjin Jing ming, called for the immediate suspension of the production of "eye with perfluoropropane gas" products. State food and drug administration after the country issued a moratorium on the sale and use of Crystal ming, Tianjin new technology development produced by the company issued the notice on ophthalmic perfluoropropane gas, called for an immediate stop to use the product.


Reported that on September 1, 2015, Nantong Nantong University hospitals in the food and drug administration service inspection reports and initiate an investigation. Since this fails to dispose of medical disputes from the end, the Council will keep a close watch on the progress, inform the relevant case information will be the first time. (Zhong Xin)



Responsible editor: Wang Hao





Article keywords:
Gases in patients with eye diseases

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Beijing times
江苏26名眼病患者被注射问题气体 部分人失明 |患者|气体|眼病_新闻资讯

  原标题:手术使用问题医疗器械 江苏26名患者眼球受损  


  京华时报讯 日前,江苏南通26名眼病患者反映,他们在南通大学附属医院注射了一种名为全氟丙烷的气体,用来治疗视网膜脱落等病症,谁知该批次医用气体属于问题医疗器械,后被国家食药监总局召回。目前,已有两名患者失明。昨天,南通大学附属医院发布通报称,这起事件系使用天津晶明新技术开发有限公司生产的眼用全氟丙烷气体引发,除对受害者采取及时补救与追踪复查外,已将该公司诉至法院。


  通报显示,使用天津晶明生产同一批次的眼用全氟丙烷气体后出现不良反应的患者共有26名,均发生在2015年6月5日至6月29日。不良反应的症状主要表现为眼内纤维素性渗出、晶状体混浊、视神经萎缩、视网膜血管阻塞等。根据专家意见对其中的23名患者分批分次连夜进行了补救手术,清除残余问题气体,填充硅油等,并持续进行密切随访和治疗。


  同时,南通大学附属医院在通报中表示,对于患者遭遇的不幸深感痛心,积极补救和追踪病人复查。


  昨天,南通市食药监局也通报称,将密切关注事态进展,相关案件信息将在第一时间通报。


  南通市食药监局通报说,2015年7月4日晚,该局接到南通大学附属医院7份不良事件报告,均涉及同一产品“眼用全氟丙烷气体”,在使用后病人发生葡萄膜炎反应,可能导致机体功能结构永久性损伤,院方已停止使用该产品并组织开展相应救治。该局当即研究处置工作并对全市产品使用情况紧急调查,同步向江苏省药品不良反应监测中心报告。次日,该局组成调查组赴医院开展现场调查,对产品生产企业资质、产品批文、购进手续、产品出厂检验报告、出入库手续、业务员的授权书等材料等进行了全面调查,对该批次产品库存全部抽样控制,派专人送中国食品药品检定研究院检测。


  2015年7月6日,该局向全市发出紧急通知,要求立即暂停使用天津晶明生产的“眼用全氟丙烷气体”产品。后国家食药监总局向全国发出《关于暂停销售使用天津晶明新技术开发有限公司生产的眼用全氟丙烷气体的通知》,要求立即停用该批产品。


  通报称,2015年9月1日,南通食药监局到南通大学附属医院送达检验报告并立案调查。由于该起医疗纠纷未处置终结,该局将密切关注事态进展,相关案件信息将在第一时间通报。(钟欣)



责任编辑:王浩成





文章关键词:
患者 气体 眼病

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