中国医学创新
中國醫學創新
중국의학창신
MEDICAL INNOVATION OF CHINA
2015年
1期
1-3
,共3页
周海平%刘锦宙%张春霞%刘莉琼%李萍%饶慧燕
週海平%劉錦宙%張春霞%劉莉瓊%李萍%饒慧燕
주해평%류금주%장춘하%류리경%리평%요혜연
肠易激综合征%草酸艾司西酞普兰%奥替溴铵
腸易激綜閤徵%草痠艾司西酞普蘭%奧替溴銨
장역격종합정%초산애사서태보란%오체추안
Irritable bowel syndrome%Escitalopram oxalate%Otilonium bromide
目的:观察奥替溴铵联合草酸艾司西酞普兰治疗肠易激综合征(IBS)的疗效。方法:按罗马Ⅲ诊断标准选择60例肠易激综合征患者,按就诊顺序奇偶数分组,奇数为研究组,偶数为对照组,各30例。入组前均进行肠易激综合征症状严重程度量表(IBS-SSS)评分,入组后12周内两组均给予奥替溴铵40 mg,tid,研究组联用草酸艾司西酞普兰10 mg/d;12周后,研究组继续服用草酸艾司西酞普兰至24周,两组在12~24周期间均根据腹痛情况按需服用奥替溴铵(不作常规服用)。分别在治疗2、4、8、12、24周末各评定一次治疗效果。结果:治疗第2、4、8、12、24周末研究组IBS-SSS评分依次为(185.00±38.24)分、(149.07±38.30)分、(127.83±37.51)分、(112.97±37.55)分、(102.97±43.82)分,对照组评分依次为(226.80±42.98)分、(183.33±41.90)分、(165.33±37.19)分、(152.30±39.41)分、(147.57±41.46)分,两组比较差异均有统计学意义(P<0.01)。结论:联合使用草酸艾司西酞普兰和奥替溴铵更能缓解患者的腹痛、腹部不适症状及排便异常现象,并能提高患者的生活质量,疗效持久,安全耐受性好,持续用药复发风险小。
目的:觀察奧替溴銨聯閤草痠艾司西酞普蘭治療腸易激綜閤徵(IBS)的療效。方法:按囉馬Ⅲ診斷標準選擇60例腸易激綜閤徵患者,按就診順序奇偶數分組,奇數為研究組,偶數為對照組,各30例。入組前均進行腸易激綜閤徵癥狀嚴重程度量錶(IBS-SSS)評分,入組後12週內兩組均給予奧替溴銨40 mg,tid,研究組聯用草痠艾司西酞普蘭10 mg/d;12週後,研究組繼續服用草痠艾司西酞普蘭至24週,兩組在12~24週期間均根據腹痛情況按需服用奧替溴銨(不作常規服用)。分彆在治療2、4、8、12、24週末各評定一次治療效果。結果:治療第2、4、8、12、24週末研究組IBS-SSS評分依次為(185.00±38.24)分、(149.07±38.30)分、(127.83±37.51)分、(112.97±37.55)分、(102.97±43.82)分,對照組評分依次為(226.80±42.98)分、(183.33±41.90)分、(165.33±37.19)分、(152.30±39.41)分、(147.57±41.46)分,兩組比較差異均有統計學意義(P<0.01)。結論:聯閤使用草痠艾司西酞普蘭和奧替溴銨更能緩解患者的腹痛、腹部不適癥狀及排便異常現象,併能提高患者的生活質量,療效持久,安全耐受性好,持續用藥複髮風險小。
목적:관찰오체추안연합초산애사서태보란치료장역격종합정(IBS)적료효。방법:안라마Ⅲ진단표준선택60례장역격종합정환자,안취진순서기우수분조,기수위연구조,우수위대조조,각30례。입조전균진행장역격종합정증상엄중정도량표(IBS-SSS)평분,입조후12주내량조균급여오체추안40 mg,tid,연구조련용초산애사서태보란10 mg/d;12주후,연구조계속복용초산애사서태보란지24주,량조재12~24주기간균근거복통정황안수복용오체추안(불작상규복용)。분별재치료2、4、8、12、24주말각평정일차치료효과。결과:치료제2、4、8、12、24주말연구조IBS-SSS평분의차위(185.00±38.24)분、(149.07±38.30)분、(127.83±37.51)분、(112.97±37.55)분、(102.97±43.82)분,대조조평분의차위(226.80±42.98)분、(183.33±41.90)분、(165.33±37.19)분、(152.30±39.41)분、(147.57±41.46)분,량조비교차이균유통계학의의(P<0.01)。결론:연합사용초산애사서태보란화오체추안경능완해환자적복통、복부불괄증상급배편이상현상,병능제고환자적생활질량,료효지구,안전내수성호,지속용약복발풍험소。
Objective: To observe the effect of Otilonium bromide combined with Oxalic acid Ai Sciplan in the treatment of irritable bowel syndrome (IBS).Method: 60 cases with irritable bowel syndrome were selected according to the Rome Ⅲ diagnosis criteria, they were grouped by the visit order of odd and even, odd as the research group, even for the control group, 30 cases in each group. Before entering the group ,they were score by irritable bowel syndrome severity scale (IBS-SSS), when enrolled the two groups were given otilonium bromide 40 mg,tid, the research group in conjunction with oxalic acid Ai Sciplan 10 mg/d within 12 weeks. After 12 weeks, the research group continues taking escitalopram oxalate to 24 weeks, the two groups used otilonium bromide according to abdominal pain duringon-demand during 12 to 24 weeks (not as a conventional take).Result: The treatment effect was evaluated respectively at the end of 2, 4, 8, 12, 24 weeks, and the IBS-SSS scores of the research group were (185.00±38.24), (149.07±38.30), (127.83±37.51), (112.97±37.55), (102.97±43.82), the control group scores were (226.80±42.98), (183.33±41.90), (165.33±37.19), (152.30±39.41), (147.57±41.46), followed by the two groups, the control group scores were significantly different (P<0.01).Conclusion: Joint use of escitalopram oxalate and otilonium bromide can ease patients abdominal pain, abdominal discomfort and abnormal bowel movements, improve the quality of life of patients at the same time. This method has lasting efficacy, safety, well tolerated, and small relapse risk when sustained drug use.