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Risedronate to Prevent Bone Loss After Sleeve Gastrectomy: Study Design and Feasibility Report of a Pilot Randomized Controlled Trial

机译:Ristronate以防止套管胃切除术后骨质损失:试点随机对照试验的研究设计和可行性报告

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Mounting evidence implicates bariatric surgery as a cause of increased skeletal fragility and fracture risk. Bisphosphonate therapy reduces osteoporotic fracture risk and may be effective in minimizing bone loss associated with bariatric surgery. The main objective of this pilot randomized controlled trial (RCT; Clinical Trial No. NCT03411902) was to determine the feasibility of recruiting, treating, and following 24 older patients who had undergone sleeve gastrectomy in a 6?month RCT examining the efficacy of 150‐mg once‐monthly risedronate (versus placebo) in the prevention of surgical weight‐loss–associated bone loss. Feasibility was defined as: (i) 30% recruitment yield, (ii) 80% retention, (iii) 80% pills taken, (iv) 80% participant satisfaction. Study recruitment occurred over 17?months. Seventy participants were referred, with 24 randomized (34% yield) to risedronate (n = 11) or placebo (n = 13). Average age was 56?±?7?years, 83% were female (63% postmenopausal), and 21% were black. The risedronate group had a higher baseline BMI than the placebo group (48.1?±?7.2 versus 41.9?±?3.8?kg/m 2 ). The 10‐year fracture risk was low (6.0% major osteoporotic fracture, 0.4% hip fracture); however, three individuals (12.5%, all risedronate group) were osteopenic at baseline. Twenty‐one participants returned for 6‐month follow‐up testing (88% retention) with all (n = 3) loss to follow‐up occurring in the risedronate group. Average number of pills taken among completers was 5.9?±?0.4 and 6.0?±?0.0 in the risedronate and placebo groups, respectively (p = 0.21), with active participants taking 80% of allotted pills. Five AEs (3.7% AE rate) were reported; one definitely related, four not related, and none serious. All participants reported high satisfaction with participation in the study. Use of bisphosphonates as a novel therapeutic to preserve bone density in patients who had undergone a sleeve gastrectomy appears feasible and well‐tolerated. Knowledge gained from this pilot RCT will be used to inform the design of an appropriately powered trial.
机译:安装证据暗示肥胖症手术是骨骼脆弱性和骨折风险增加的原因。双膦酸盐治疗可降低骨质疏松性裂缝风险,并可最大限度地减少与畜分手术相关的骨质流失。该试点随机对照试验的主要目标(RCT;临床试验号NCT03411902)是确定招生,治疗和后24名患者的可行性在6?月RCT中恢复睡眠胃切除术后的患者,检查效果150- Mg一次每月隆起(与安慰剂)预防手术减肥相关的骨质损失。可行性定义为:(i)> 30%招生产量,(ii)> 80%保留,(iii)> 80%药丸,(iv)80%的参与者满意度。学习招聘发生超过17个月。几个月。提到了七十名参赛者,24例随机(34%产率)至射出量(n = 11)或安慰剂(n = 13)。平均年龄为56°?±7?岁月,83%是女性(绝经后的63%),21%是黑色的。 ristronate组比安慰剂组具有更高的基线BMI(48.1?±7.2与41.9?3.8?3.8?kg / m 2)。 10年的骨折风险低(主要骨质疏松骨折6.0%,髋关节骨折0.4%);然而,三个人(12.5%,所有Ristronate Group)在基线上是骨质型。二十一名参与者返回6个月的后续测试(88%的保留),并在日本利用赛集团中发生所有(n = 3)损失。分别(P = 0.21)分别为5.9?±0.4和6.0?±0.4和6.0?±0.4±0.4,6.0?±0.4和6.0?±0.6 = 0.21),积极参与者采用占分配丸的80%。报告了五个AES(3.7%的AE率);一个肯定相关,四个无关,没有严重。所有参与者都与参与研究报告过高满意。使用双膦酸盐作为一种新的治疗方法,以保持经过套管胃切除术的患者骨密度似乎可行和耐受良好。从这个试点RCT获得的知识将用于通知设计适当的动力试验。

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