中国当代医药
中國噹代醫藥
중국당대의약
PERSON
2014年
30期
68-69,72
,共3页
郭迪斌%居艳娟%李荣平%谷晓晶
郭迪斌%居豔娟%李榮平%穀曉晶
곽적빈%거염연%리영평%곡효정
依托考昔%美洛昔康%急性痛风%安全性
依託攷昔%美洛昔康%急性痛風%安全性
의탁고석%미락석강%급성통풍%안전성
Etoricoxib%Meloxicam%Acute gout%Safety
目的:比较依托考昔与美洛昔康治疗急性痛风的临床效果及其用药安全性。方法选择2010年1月~2013年1月本院收治的急性痛风患者120例为研究对象,随机分为依托考昔组及美洛昔康组,每组60例。依托考昔组服用依托考昔120 mg/d,美洛昔康组服用美洛昔康15 mg/d,测定患者疼痛的自我评分并记录药物不良反应。结果治疗后,两组患者的疼痛评分均下降,且依托考昔组的疼痛改善情况明显优于美洛昔康组(P<0.05)。依托考昔组不良反应发生率为30.0%,美洛昔康组不良反应发生率为33.3%,两组差异无统计学意义(P跃0.05)。结论依托考昔治疗急性痛风的临床效果优于美洛昔康。
目的:比較依託攷昔與美洛昔康治療急性痛風的臨床效果及其用藥安全性。方法選擇2010年1月~2013年1月本院收治的急性痛風患者120例為研究對象,隨機分為依託攷昔組及美洛昔康組,每組60例。依託攷昔組服用依託攷昔120 mg/d,美洛昔康組服用美洛昔康15 mg/d,測定患者疼痛的自我評分併記錄藥物不良反應。結果治療後,兩組患者的疼痛評分均下降,且依託攷昔組的疼痛改善情況明顯優于美洛昔康組(P<0.05)。依託攷昔組不良反應髮生率為30.0%,美洛昔康組不良反應髮生率為33.3%,兩組差異無統計學意義(P躍0.05)。結論依託攷昔治療急性痛風的臨床效果優于美洛昔康。
목적:비교의탁고석여미락석강치료급성통풍적림상효과급기용약안전성。방법선택2010년1월~2013년1월본원수치적급성통풍환자120례위연구대상,수궤분위의탁고석조급미락석강조,매조60례。의탁고석조복용의탁고석120 mg/d,미락석강조복용미락석강15 mg/d,측정환자동통적자아평분병기록약물불량반응。결과치료후,량조환자적동통평분균하강,차의탁고석조적동통개선정황명현우우미락석강조(P<0.05)。의탁고석조불량반응발생솔위30.0%,미락석강조불량반응발생솔위33.3%,량조차이무통계학의의(P약0.05)。결론의탁고석치료급성통풍적림상효과우우미락석강。
Objective To analyze the clinical effect and safety of etoricoxib and meloxicam in treating acute gout. Methods 120 cases of patients with acute gout treated in our hospital from January 2010 to January 2013 were selected as research objects and were divided into etoricoxib group and meloxicam group randomly,each group for 60 cases. Etoricoxib group were treated with etoricoxib,120 mg/d.Meloxicam group were treated with meloxicam,15 mg/d.The self score of pain of patients was measured,and the adverse reactions were recorded. Results After treatment,the joint pain scores of two groups were down,and etoricoxib group improved more better than that of meloxicam group,the differences were sinificant (P<0.05).The incidence of etoricoxib group was 30.0%,and the meloxicam group was 33.3%, there was no significant difference between the two groups (P>0.05). Conclusion The clinical efficacy of etoricoxib is better than that of meloxicam.