Network meta-analysis of current drug options for the treatment of osteoporosis in men .
OrthoEvidence Journal (OE Journal) - ACE Report
OE Journal. 2015;3(15):5 PLoS One. 2015 May 26;10(5):e012803213 studies with a total of 3647 men were included in this meta-analysis to analyze the effect of eight drugs (alfacalcidol, alendronate, ibandronate, risedronate, zoledronate, strontium ranelate, teriparatide, and parathyroid hormone) on bone mass density (BMD) in the lumbar spine (LS) and fracture incidence in males with osteoporosis. Network meta-analysis based on direct and indirect comparisons demonstrated that zoledronate had the greatest efficacy in increasing BMD in LS when compared to placebo, and teriparatide had the greatest efficacy in reducing fracture rate when compared to placebo.
Were the search methods used to find evidence (original research) on the primary question or questions stated?
Was the search for evidence reasonably comprehensive?
Were the criteria used for deciding which studies to include in the overview reported?
Was the bias in the selection of studies avoided?
Were the criteria used for assessing the validity of the included studies reported?
Was the validity of all of the studies referred to in the text assessed with use of appropriate criteria (either in selecting the studies for inclusion or in analyzing the studies that were cited)?
Were the methods used to combine the findings of the relevant studies (to reach a conclusion) reported?
Were the findings of the relevant studies combined appropriately relative to the primary question that the overview addresses?
Were the conclusions made by the author or authors supported by the data and or analysis reported in the overview?
How would you rate the scientific quality of this evidence?
نعم = 1
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غير ذي صلة = 0
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يقيّم تقييم معايير الإبلاغ الشفافية التي يبلغ بها المؤلفون عن الخصائص المنهجية والتجريبية للتجربة في المنشور. ينقسم التقييم إلى خمس فئات معروضة أدناه.
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Introduction
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Accessing Data
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Analysing Data
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Results
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Discussion
Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65
مؤشر الهشاشة هو أداة تساعد في تفسير النتائج المهمة، وتوفر مقياسًا لقوة النتيجة. ويمثل مؤشر الهشاشة عدد الأحداث المتتالية التي يجب إضافتها إلى نتيجة ثنائية التفرع لجعل النتيجة غير مهمة. يمثل الرقم الصغير نتيجة أضعف ويمثل الرقم الكبير نتيجة أقوى.
لماذا كانت هناك حاجة لهذه الدراسة الآن؟
Osteoporosis is a common bone disease that results in decreased bone mass, and in turn significantly increases the risk of fracture. An improvement of bone mass density has been demonstrated to minimize the incidence of osteoporotic fractures. There have been a number of drugs which have been suggested to be efficacious in osteoporosis treatment, such as bisphosphonates (including alendronate, risedronate, ibandronate, and zoledronate), bone-anabolic drugs of parathyroid or teriparatide, strontium ranelate, and alfacalcidol, a vitamin D analog. Due to the wide range of drugs available, and conflicting results from many randomized controlled trials, the study sought to compare these options for primary treatment of osteoporosis.
ما هو سؤال البحث الرئيسي؟
Between available drug therapies for osteoporosis (alfacalcidol, alendronate, ibandronate, risedronate, zoledronate, strontium ranelate, teriparatide, and parathyroid hormone) what is the hierarchy of efficacy with respect to improvement in bone mineral density of the lumbar spine and reduction of fracture rate?
- Compared to placebo, effect on lumbar spine BMD from greatest to lowest was zoledronate (SMD 13.48 [95% CrI 11.88 to 15.08]), alendronate (11.04 [9.68 to 12.41]), teriparatide (20mcg) + risedronate (10.98 [8.55 to 13.48]), risedronate (10.33 [8.68 to 12.01]), teriparatide (20mcg) (9.33 [6.87 to 11.76]), strontium ranelate (8.88 [7.51 to 10.24]), ibandronate (5.49 [3.82 to 7.16]), parathyroid hormone (4.89 [3.12 to 6.62]) and alfacalcidol (3.42 [1.7 to 5.2]).
- With the exception of teriparatide (20mcg) + risedronate, zoledronate demonstrated a significantly greater effect size on LS BMD when compared to all other treatment options.
- Compared to placebo, significantly lower fracture rates were demonstrated with treatment with teriparatide (20mcg) (4.04 [1.36 to 8.49]), teriparatide (40mcg) (3.5 [1.14 to 8.34]), zoledronate (2.92 [1.29 to 5.62]), and risedronate (OR 2.51 [95%CrI 1.23 to 4.24]).
- Alfacalcidol was associated with significantly higher fracture rate than treatment with risedronate (7.66, 1.74 to 19.27), zoledronate (8.41, 2.12 to 20.03), strontium ranelate (5.21, 1.32 to 11.88), teriparatide (40mcg) (10.49, 1.83 to 30.47), or teriparatide (20mcg) (12.12, 2.17 to 33.84)
ما الذي يجب أن أتذكره أكثر؟
In osteoporosis treatment in men, zoledronate was associated with the greatest effect on lumbar spine bone mineral density relative to placebo treatment. Among the drug options, zoledronate, risedronate, and teriparatide (20 or 40mcg) demonstrated significant reductions in fracture incidence compared to placebo.
كيف سيؤثر ذلك على رعاية مرضاي؟
The results of this study offer a preliminary analysis on the current evidence regarding effect of current drug options for osteoporosis on bone mineral density increase and fracture risk reduction. In general, zoledronate may be the most effective therapy drug for increasing lumbar BMD, whereas teriparatide may be associated with the greatest reduction in fracture rate. Nevertheless, results should be interpreted with careful consideration, as head-to-head comparisons between each drug are needed to ultimately conclude which treatment option offers the greatest efficacy for men with osteoporosis. Additional, future trials should consider safety analyses associated with the treatment options evaluated in the current study.
تنويه
هذا المحتوى الموجود في هذه الصفحة هو لأغراض إعلامية فقط وليس الغرض منه أن يكون بديلاً عن المشورة الطبية المتخصصة أو التشخيص أو العلاج. إذا كنت بحاجة إلى علاج طبي، اطلب دائمًا مشورة طبيبك أو اذهب إلى أقرب قسم طوارئ إليك. الآراء والمعتقدات ووجهات النظر التي يعبر عنها الأفراد في المحتوى الموجود في هذه الصفحة لا تعكس آراء ومعتقدات ووجهات نظر أورثوإيفيدنس.