中国临床康复
中國臨床康複
중국림상강복
CHINESE JOURNAL OF CLINICAL REHABILITATION
2004年
24期
5182-5183
,共2页
朱秀英%张延桥%裴丽春%李旋%于卫刚
硃秀英%張延橋%裴麗春%李鏇%于衛剛
주수영%장연교%배려춘%리선%우위강
骨质疏松%脊柱骨折%药物疗法%处方,药物
骨質疏鬆%脊柱骨摺%藥物療法%處方,藥物
골질소송%척주골절%약물요법%처방,약물
背景:骨质疏松性脊椎骨折是绝经后妇女和老年女性最常见的骨折类型.优选哪类药物及治疗处方对其治疗会产生最优效果和最小副作用正在研究中.目的:观察钙三醇、依替膦酸二钠、枸橼酸钙联合治疗骨质疏松性脊椎骨折临床效果及副作用.设计:自身对照研究.地点和对象:2001-01/2003~04哈尔滨医科大学第二附属医院门诊和住院患者中诊断骨质疏松性脊椎骨折患者25例,男4例,女21例;年龄59~98岁,平均(74±10)岁,原发性骨质疏松症20例,继发性骨质疏松症5例.干预:给予钙三醇0.5μg,1次/d口服,枸橼酸钙3片,3次/d口服,两药连续应用10~11周;依替膦酸二钠0.2 g,2次/d两餐之间口服,连用2周.3种药共用12~13周(3个月)为1个周期.主要观察指标:①用药前后骨痛缓解情况.②骨密度值.③其他症状的改善情况.结果:服药1个月临床骨痛症状开始缓解,3个月大部分患者骨痛明显缓解,半年后骨痛症状基本消失.骨密度测定,用药半年后,全部患者L2~4骨量均有升高,均值骨密度升高0.098 g/cm2,未出现新骨折,患者对药物耐量性好无明显副作用.结论:钙三醇、依替膦酸二钠、枸橼酸钙联合治疗骨质疏松性骨折临床疗效好,效果肯定,无明显药物不良反应,患者耐受性、依从性好,可做为治疗骨质疏松性脊椎骨折的首选治疗处方.
揹景:骨質疏鬆性脊椎骨摺是絕經後婦女和老年女性最常見的骨摺類型.優選哪類藥物及治療處方對其治療會產生最優效果和最小副作用正在研究中.目的:觀察鈣三醇、依替膦痠二鈉、枸櫞痠鈣聯閤治療骨質疏鬆性脊椎骨摺臨床效果及副作用.設計:自身對照研究.地點和對象:2001-01/2003~04哈爾濱醫科大學第二附屬醫院門診和住院患者中診斷骨質疏鬆性脊椎骨摺患者25例,男4例,女21例;年齡59~98歲,平均(74±10)歲,原髮性骨質疏鬆癥20例,繼髮性骨質疏鬆癥5例.榦預:給予鈣三醇0.5μg,1次/d口服,枸櫞痠鈣3片,3次/d口服,兩藥連續應用10~11週;依替膦痠二鈉0.2 g,2次/d兩餐之間口服,連用2週.3種藥共用12~13週(3箇月)為1箇週期.主要觀察指標:①用藥前後骨痛緩解情況.②骨密度值.③其他癥狀的改善情況.結果:服藥1箇月臨床骨痛癥狀開始緩解,3箇月大部分患者骨痛明顯緩解,半年後骨痛癥狀基本消失.骨密度測定,用藥半年後,全部患者L2~4骨量均有升高,均值骨密度升高0.098 g/cm2,未齣現新骨摺,患者對藥物耐量性好無明顯副作用.結論:鈣三醇、依替膦痠二鈉、枸櫞痠鈣聯閤治療骨質疏鬆性骨摺臨床療效好,效果肯定,無明顯藥物不良反應,患者耐受性、依從性好,可做為治療骨質疏鬆性脊椎骨摺的首選治療處方.
배경:골질소송성척추골절시절경후부녀화노년녀성최상견적골절류형.우선나류약물급치료처방대기치료회산생최우효과화최소부작용정재연구중.목적:관찰개삼순、의체련산이납、구연산개연합치료골질소송성척추골절림상효과급부작용.설계:자신대조연구.지점화대상:2001-01/2003~04합이빈의과대학제이부속의원문진화주원환자중진단골질소송성척추골절환자25례,남4례,녀21례;년령59~98세,평균(74±10)세,원발성골질소송증20례,계발성골질소송증5례.간예:급여개삼순0.5μg,1차/d구복,구연산개3편,3차/d구복,량약련속응용10~11주;의체련산이납0.2 g,2차/d량찬지간구복,련용2주.3충약공용12~13주(3개월)위1개주기.주요관찰지표:①용약전후골통완해정황.②골밀도치.③기타증상적개선정황.결과:복약1개월림상골통증상개시완해,3개월대부분환자골통명현완해,반년후골통증상기본소실.골밀도측정,용약반년후,전부환자L2~4골량균유승고,균치골밀도승고0.098 g/cm2,미출현신골절,환자대약물내량성호무명현부작용.결론:개삼순、의체련산이납、구연산개연합치료골질소송성골절림상료효호,효과긍정,무명현약물불량반응,환자내수성、의종성호,가주위치료골질소송성척추골절적수선치료처방.
BACKGROUND: Osteoporotic vertebral fracture is major fracture in post-menopause women and aged women. Optimal drugs and therapies are under study. The Optimization effect and the minimum side effect are also on study.OBJECTIVE: To observe the clinical efficacy and side effects of the combined treatment of Rocaltrol, Etidronate and Sisterly for osteoporotic vertebral fracture.DESIGN: A self-controlled trial.SETTING and PARTICIPANTS: Twenty-five patients with osteoporotic vertebral fracture from the Second Affiliated Hospital of Harbin Medical University were included in the study from January 2001 to March 2003 (4 men and 21 women; mean age: (74±10), range: 59 -98), including 20 patients of primary osteoporosis, and 5 patients of secondary osteoporosis.INTERVENTIONS: Rocaltrol, 0.5μg, was orally administered once every day and Sisterly 3 tablets bid after each meal. Both drugs were applied for consecutive 10- 11 weeks. Then Etidronate was added, 0.2 g bid between two meals for consecutive two weeks. The combined therapy of these three drugs were used for 12 - 13 weeks(3 months) as a cycle. MAIN OUTCOME MEASURES: Bone pain before and after drug; bone mineral density; and other symptoms.RESULTS: Bone pain was slightly relieved one month after therapy and apparently relieved three months later. After six months of treatment, bone pain almost disappeared. Bone mineral density of L2-4 in all the patients increased by 0. 098 g/cm2(mean) and no new bone fracture was found. All patients tolerated these three medicines well and no obvious side effect was observed.CONCLUSION: The combined therapy of Rocaltrol, Etidronate and Sisterly have good effects on osteoporotic vertebral fracture without obvious side effects. Patients have good toleration and good compliance. It can be used as the first-line therapy for osteoporotic vertebral fracture.