药品评价
藥品評價
약품평개
DRUG REEVALUATION
2014年
13期
27-29,47
,共4页
史双伟%郑丽丽%李冲%王志芳%张佳楠%张淑君%刘真真
史雙偉%鄭麗麗%李遲%王誌芳%張佳楠%張淑君%劉真真
사쌍위%정려려%리충%왕지방%장가남%장숙군%류진진
维格列汀%胰岛素%联合治疗%2型糖尿病
維格列汀%胰島素%聯閤治療%2型糖尿病
유격렬정%이도소%연합치료%2형당뇨병
Vildagliptin%Insulin%Combination therapy%Type 2 diabetes mellitus
目的:研究在接受胰岛素治疗的2型糖尿病患者中,联合应用维格列汀治疗的疗效及对胰岛素剂量的影响并进行安全性评价。方法:本实验为前瞻性、开放性、前后自身及空白对照的临床研究。设立试验组和对照组,试验组为110例应用胰岛素治疗的2型糖尿病患者,加用维格列汀50mg,每日2次,治疗12周,对照组为109例应用胰岛素治疗12周的患者,观察两组治疗前后糖化血红蛋白(HbA1c)及血糖变化。结果:治疗12周后,试验组HbA1c由基线的(9.27±1.42)%降至(7.82±1.36)%,下降了(1.45±1.03)%,对照组HbA1c由基线的(8.86±1.06)%降至(8.02±1.32)%,下降了(0.84±1.13)%,两组下降幅度均P<0.05。以HbA1c≤6.5%和HbA1c≤7.0%为目标值,治疗后试验组达标率为16.36%和43.63%,较治疗前增加12.76%和33.63%;试验组胰岛素用量由基线的53.9IU/d降至41.2IU/d,剂量减少23.56%,对照组胰岛素用量由基线的66.7IU/d降至58.3IU/d,剂量减少12.59%,两组胰岛素减少量P<0.05;患者空腹血糖及餐后2h血糖均有明显改善;患者平均每日药品费用较治疗前无明显增加(P>0.05)。治疗期间试验组共14例患者(12.7%)发生一般性低血糖事件(24件·次),无严重低血糖事件发生,与对照组比较,低血糖发生率有统计学差异(P<0.05)。结论:维格列汀联合胰岛素治疗2型糖尿病,可有效降低患者空腹及餐后血糖水平,利于实现HbA1c达标,并减少胰岛素使用剂量,提高治疗的安全性及耐受性。
目的:研究在接受胰島素治療的2型糖尿病患者中,聯閤應用維格列汀治療的療效及對胰島素劑量的影響併進行安全性評價。方法:本實驗為前瞻性、開放性、前後自身及空白對照的臨床研究。設立試驗組和對照組,試驗組為110例應用胰島素治療的2型糖尿病患者,加用維格列汀50mg,每日2次,治療12週,對照組為109例應用胰島素治療12週的患者,觀察兩組治療前後糖化血紅蛋白(HbA1c)及血糖變化。結果:治療12週後,試驗組HbA1c由基線的(9.27±1.42)%降至(7.82±1.36)%,下降瞭(1.45±1.03)%,對照組HbA1c由基線的(8.86±1.06)%降至(8.02±1.32)%,下降瞭(0.84±1.13)%,兩組下降幅度均P<0.05。以HbA1c≤6.5%和HbA1c≤7.0%為目標值,治療後試驗組達標率為16.36%和43.63%,較治療前增加12.76%和33.63%;試驗組胰島素用量由基線的53.9IU/d降至41.2IU/d,劑量減少23.56%,對照組胰島素用量由基線的66.7IU/d降至58.3IU/d,劑量減少12.59%,兩組胰島素減少量P<0.05;患者空腹血糖及餐後2h血糖均有明顯改善;患者平均每日藥品費用較治療前無明顯增加(P>0.05)。治療期間試驗組共14例患者(12.7%)髮生一般性低血糖事件(24件·次),無嚴重低血糖事件髮生,與對照組比較,低血糖髮生率有統計學差異(P<0.05)。結論:維格列汀聯閤胰島素治療2型糖尿病,可有效降低患者空腹及餐後血糖水平,利于實現HbA1c達標,併減少胰島素使用劑量,提高治療的安全性及耐受性。
목적:연구재접수이도소치료적2형당뇨병환자중,연합응용유격렬정치료적료효급대이도소제량적영향병진행안전성평개。방법:본실험위전첨성、개방성、전후자신급공백대조적림상연구。설립시험조화대조조,시험조위110례응용이도소치료적2형당뇨병환자,가용유격렬정50mg,매일2차,치료12주,대조조위109례응용이도소치료12주적환자,관찰량조치료전후당화혈홍단백(HbA1c)급혈당변화。결과:치료12주후,시험조HbA1c유기선적(9.27±1.42)%강지(7.82±1.36)%,하강료(1.45±1.03)%,대조조HbA1c유기선적(8.86±1.06)%강지(8.02±1.32)%,하강료(0.84±1.13)%,량조하강폭도균P<0.05。이HbA1c≤6.5%화HbA1c≤7.0%위목표치,치료후시험조체표솔위16.36%화43.63%,교치료전증가12.76%화33.63%;시험조이도소용량유기선적53.9IU/d강지41.2IU/d,제량감소23.56%,대조조이도소용량유기선적66.7IU/d강지58.3IU/d,제량감소12.59%,량조이도소감소량P<0.05;환자공복혈당급찬후2h혈당균유명현개선;환자평균매일약품비용교치료전무명현증가(P>0.05)。치료기간시험조공14례환자(12.7%)발생일반성저혈당사건(24건·차),무엄중저혈당사건발생,여대조조비교,저혈당발생솔유통계학차이(P<0.05)。결론:유격렬정연합이도소치료2형당뇨병,가유효강저환자공복급찬후혈당수평,리우실현HbA1c체표,병감소이도소사용제량,제고치료적안전성급내수성。
Objective:To investigate the efficacy and safety of vildagliptin combined with insulin in patients with type 2 diabetes mellitus, and if the insulin dosage induced or not. Methods: Type 2 diabetic patients treated with insulin were enrolled in this prospective open-labeled and self-controlled study. Vildagliptin added to 110 patients for 12 weeks were treatment group, another 109 patients without vildagliptin were control group. Results:HbA1cof the treatment group decreased from 9.27±1.42%to 7.82±1.36%(P<0.05). HbA1cof the control group decreased from 8.86±1.06%to 8.02±1.32%(P<0.05). About 12.76% and 33.63% patients of the treatment group obtained the target of HbAIc≤6.5% and HbAIc≤7.0%. Insulin dose of the treatment group decreased from 53.9IU/d to 41.3IU/d (decreased 23.56%), the other decreased from 66.7IU/d to 58.3IU/d (decreased 12.59%), P<0.05. The blood glucose profile was also improved significantly. The daily drug cost was not increased, P>0.05. During the study period,14 patients (12.7%) of the treatment group experienced with minor hypoglycemia for 24 times, no serious hypoglycemia was reported. The differ was significant compared with control group. Conclusion:Vildagliptin combined with insulin is efficient and safe in type 2 diabetic patients, therefore can decrease insulin dosage and the therapeutic risks of insulin.