期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
聚乙二醇3350缓泻药治疗便秘效果缺乏持久性 被引量:1
1
作者 Tran L.C. Di Palma J.A. 纪泛扑 《世界核心医学期刊文摘(胃肠病学分册)》 2005年第12期40-40,共1页
Purpose: PEG 3350 (MiraLax, Braintree Laboratories Inc., Braintree, MA) 17 g daily has been shown to be safe and effective in a 14- day trial for constipation. This present investigation was designed to extend the tre... Purpose: PEG 3350 (MiraLax, Braintree Laboratories Inc., Braintree, MA) 17 g daily has been shown to be safe and effective in a 14- day trial for constipation. This present investigation was designed to extend the treatment and safety experience with PEG 3350 and to evaluate any lasting effectiveness during a 30- day post- treatment observation period. Methods: Study subjects met Rome II criteria for constipation and reported< 3 bowel movements a week. They were treated with PEG 3350 17 g daily for 14 days. Treatment efficacy was defined by resolution of constipation symptoms as determined by the Rome II and stool frequency definitions during the treatment period. Results: Fifty healthy constipated subjects formed the study group. There were 42 females and 8 males. Mean age was 52 ± 15.5 years (± SD). Symptom duration was 22.6 ± 16.7 months (± SD). At baseline, all had< 3 bowel movements a week and met Rome II criteria. Two were lost to follow- up. Two took enemas or laxatives and 2 discontinued active treatment because of “ gas" and were considered treatment failures. At the end of 14 days, 40 of 48 (83.3% ) had >3 stools in the last week and no longer met Rome criteria. Thirty- two of 45 (71.1% ) reported satisfaction with the first bowel movement after initiating treatment. Thirty days after active treatment, 29 of 47 (61.7% ) responded that they needed laxative treatment. Conclusion: PEG 3350 relieved constipation in most treated study subjects. During a 30- day post- treatment observation period, 29 of 47 (61.7% ) had additional constipation treatment interventions. 展开更多
关键词 缓泻药 持久性 诊断标准 健康受试者 肠胀气 安全性试验 失访
下载PDF
Psoriatic skin lesions induced by tumor-necrosis-factor-alpha-therapy
2
作者 Antonia Cosima Faul Christian Folwaczny +3 位作者 Birgit Angela Aigner Rüdiger Hein Johannes Ring Sabine Gisela Plotz 《Case Reports in Clinical Medicine》 2013年第1期85-88,共4页
A 46-year-old, caucasian woman suffering from Crohn’s disease and a 35-year-old woman suffering from ankylosing spondylitis were treated with the TNFα blocker infliximab and developed psoriasiform skin lesions. The ... A 46-year-old, caucasian woman suffering from Crohn’s disease and a 35-year-old woman suffering from ankylosing spondylitis were treated with the TNFα blocker infliximab and developed psoriasiform skin lesions. The pathophysiology of this paradoxical clinical response as a newly recognized adverse effect of TNFα antagonists is unknown. According to the literature, this type of newly triggered psoriasis may occur any time after initiation of TNFα antagonist therapy and responds to classic antipsoriatic treatment. The phenomenon warrants attention, especially when considering anti-TNFα treatment in various skin diseases besides psoriasis. 展开更多
关键词 INFLIXIMAB PSORIASIS TNFαInhibitors Crohn’s Disease Ankylosing Spondylitis Side Effects
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部