Chodorowski Zygmunt, Sein Anand Jacek
Katedra i Klinika Chorób Wewnetrznych, Geriatrii i Toksykologii Klinicznej, Akademii Medycznej w Gdańsku.
Przegl Lek. 2007;64(4-5):365-7.
In the article some merits and some limitations of inhaled insulin (Exubera produced by Pfizer) in the treatment of adult patients with type 1 or 2 diabetes were presented. Up till now about 3500 volunteers usually in short-term study periods (6 months) were examined. Some patients were observed in the course of treatment even 4-7 years. Inhaled insulin was well tolerated by patients and they accepted with satisfaction this new form of drug. Main adverse events were a small decrease in the forced expiratory volume at 1 s (FEV1) and a small decline in carbon monoxide diffusion capacity with no clinical significance a well as a mild or moderate cough occurring temporally. Inhaled insulin is contraindicated in smokers and patients with bronchial asthma, bronchitis and pulmonary emphysema. Despite the approval of inhaled insulin for use in adult patients with type 1 or 2 diabetes in the United States and European Union in January 2006, Pfizer designed Real World Trial to estimate the costleffectiveness of this drug and the effect of the availability of Exubera as a treatment options for glycemic control.
该文章介绍了吸入式胰岛素(辉瑞公司生产的Exubera)在治疗1型或2型糖尿病成年患者中的一些优点和局限性。截至目前,约3500名志愿者通常在短期研究阶段(6个月)接受了检查。部分患者在治疗过程中甚至被观察了4至7年。患者对吸入式胰岛素耐受性良好,并且对这种新剂型药物满意度较高。主要不良事件为1秒用力呼气量(FEV1)略有下降、一氧化碳弥散量略有降低,但无临床意义,以及偶尔出现轻度或中度咳嗽。吸烟者、支气管哮喘患者、支气管炎患者和肺气肿患者禁用吸入式胰岛素。尽管2006年1月吸入式胰岛素已在美国和欧盟获批用于治疗1型或2型糖尿病成年患者,但辉瑞公司仍开展了“真实世界试验”,以评估该药物的成本效益以及Exubera作为血糖控制治疗选择的可及性影响。