中国骨质疏松杂志
中國骨質疏鬆雜誌
중국골질소송잡지
CHINESE JOURNAL OF OSTEOPOROSIS
2014年
7期
820-823
,共4页
原发性骨质疏松%唑来膦酸%疗效%不良反应
原髮性骨質疏鬆%唑來膦痠%療效%不良反應
원발성골질소송%서래련산%료효%불량반응
Primary osteoporosis%Zoledronic acid%Effectiveness%Adverse effects
目的:本研究通过与口服阿仑膦酸钠( alendronate sodium)的对比,旨在评价老年人使用唑来膦酸注射液( zoledronic acid)的疗效、应用、安全性、依从性。方法回顾性分析2012年8月至2013年9月,重庆医科大学附属第一医院的116例原发性骨质疏松患者的医疗记录。两组药物组各包含58例,选取绝经后妇女、60岁以上原发性骨质疏松患者且首次使用阿仑膦酸钠/唑来膦酸注射液患者入组。通过对比两组用药前后腰椎和(或)髋部骨密度改变、依从性、不良反应和新发骨折率,比较两种药物的疗效。结果两组入组患者性别、年龄、骨密度相似。唑来膦酸注射液组的骨密度增加量比阿仑膦酸钠组有显著差异,其中腰椎骨密度(P=0.007)、髋部骨密度(P=0.006)。唑来膦酸注射液组有更多的不良反应(n=50);新发骨折数较阿仑膦酸钠组少( n=12)。两组患者中,疼痛为主的主观症状以视觉模拟标度尺( visual analogue scale,VAS)表示,唑来膦酸注射液组中疼痛症状明显缓解( P<0.01)。两组中治疗前后血钙( blood calcium,BC)和碱性磷酸酶( alkaline phosphatase,AP)均无明显差异。结论唑来膦酸注射液治疗老年性骨质疏松更优于阿仑膦酸钠。在提高腰椎及髋部骨密度方面疗效相似。虽然在治疗前3天有更多的不良反应,但减少了新发骨折率,缓解症状更显著。两组药物对血生化的影响均无明显差异。
目的:本研究通過與口服阿崙膦痠鈉( alendronate sodium)的對比,旨在評價老年人使用唑來膦痠註射液( zoledronic acid)的療效、應用、安全性、依從性。方法迴顧性分析2012年8月至2013年9月,重慶醫科大學附屬第一醫院的116例原髮性骨質疏鬆患者的醫療記錄。兩組藥物組各包含58例,選取絕經後婦女、60歲以上原髮性骨質疏鬆患者且首次使用阿崙膦痠鈉/唑來膦痠註射液患者入組。通過對比兩組用藥前後腰椎和(或)髖部骨密度改變、依從性、不良反應和新髮骨摺率,比較兩種藥物的療效。結果兩組入組患者性彆、年齡、骨密度相似。唑來膦痠註射液組的骨密度增加量比阿崙膦痠鈉組有顯著差異,其中腰椎骨密度(P=0.007)、髖部骨密度(P=0.006)。唑來膦痠註射液組有更多的不良反應(n=50);新髮骨摺數較阿崙膦痠鈉組少( n=12)。兩組患者中,疼痛為主的主觀癥狀以視覺模擬標度呎( visual analogue scale,VAS)錶示,唑來膦痠註射液組中疼痛癥狀明顯緩解( P<0.01)。兩組中治療前後血鈣( blood calcium,BC)和堿性燐痠酶( alkaline phosphatase,AP)均無明顯差異。結論唑來膦痠註射液治療老年性骨質疏鬆更優于阿崙膦痠鈉。在提高腰椎及髖部骨密度方麵療效相似。雖然在治療前3天有更多的不良反應,但減少瞭新髮骨摺率,緩解癥狀更顯著。兩組藥物對血生化的影響均無明顯差異。
목적:본연구통과여구복아륜련산납( alendronate sodium)적대비,지재평개노년인사용서래련산주사액( zoledronic acid)적료효、응용、안전성、의종성。방법회고성분석2012년8월지2013년9월,중경의과대학부속제일의원적116례원발성골질소송환자적의료기록。량조약물조각포함58례,선취절경후부녀、60세이상원발성골질소송환자차수차사용아륜련산납/서래련산주사액환자입조。통과대비량조용약전후요추화(혹)관부골밀도개변、의종성、불량반응화신발골절솔,비교량충약물적료효。결과량조입조환자성별、년령、골밀도상사。서래련산주사액조적골밀도증가량비아륜련산납조유현저차이,기중요추골밀도(P=0.007)、관부골밀도(P=0.006)。서래련산주사액조유경다적불량반응(n=50);신발골절수교아륜련산납조소( n=12)。량조환자중,동통위주적주관증상이시각모의표도척( visual analogue scale,VAS)표시,서래련산주사액조중동통증상명현완해( P<0.01)。량조중치료전후혈개( blood calcium,BC)화감성린산매( alkaline phosphatase,AP)균무명현차이。결론서래련산주사액치료노년성골질소송경우우아륜련산납。재제고요추급관부골밀도방면료효상사。수연재치료전3천유경다적불량반응,단감소료신발골절솔,완해증상경현저。량조약물대혈생화적영향균무명현차이。
Objective To assess real-life effectiveness, health care resource utilization, safety, and compliance to the treatment with zoledronic acid in comparison with orally administered alendronate sodium in senile patients with osteoporosis.Methods The medical records of 116 patients with primary osteoporosis, who were treated in the First Affiliated Hospital of Chongqing Medical University from August 2012 to September 2013, were retrospectively analyzed.The study cohort consisted of 58 patients treated with each drug.Eligible patients were postmenopausal females and males over 60 years old with osteoporosis, and first time use of alendronate sodium or zoledronic acid.Outcomes were the changes of the bone mineral density ( BMD) of the lumbar vertebrae and the hip, the adherence, the adverse effects, and the occurrence of new fractures in patients.Results Patients in both groups were similar with regards to sex, age, and BMD.The increase of BMD in zoledronic acid group was more significant than that in alendronate sodium group, including BMD of the lumbar vertebrae (P=0.007) and the hip (P=0.006).Zoledronic acid group had more adverse effects (n=50).Meanwhile, the number of patients with new fracture (n=3) was less than that in alendronate sodium group ( n =12 ) .The subjective symptoms were measured with visual analogue scale ( VAS ) and the pain scores.In zoledronic acid group, the pain significantly reduced ( P<0.01) .The blood calcium ( BC) and alkaline phosphatase ( AP) were in the normal ranges before and after the treatment in both groups.Conclusion Zoledronic acid has advantages over alendronate sodium in treating senile osteoporosis.They can increase BMD of the lumbar vertebrae and the hip the same.While patients in zoledronic acid group have more adverse effects in the first 3 days, it can reduce the occurrence of fresh fracture.It also reduces the subjective symptoms markedly.Both drugs appear to be safe in terms of blood calcium and alkaline phosphatase.