颌骨药物相关性骨坏死发生后骨质疏松症的处理:一个三级医疗中心13年的经验。

Chun Ho Wong, Kimberly Hang Tsoi, Jingya Jane Pu, Nancy Su Jiang, Stacey Sheung Yi Chan, Connie Hong Nin Loong, Xincheng Zou, Carol Ho Yi Fong, Eunice Ka Hong Leung, Alan Chun Hong Lee, Chi Ho Lee, Kathryn Choon Beng Tan, Yu Cho Woo, Yu-Xiong Su, David Tak Wai Lui
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引用次数: 0

摘要

背景:我们研究了药物相关性颌骨骨坏死(MRONJ)发生后骨质疏松症的管理策略和临床结果。方法:我们回顾性研究了2010年至2022年间在香港玛丽医院骨质疏松中心或口腔颌面外科及牙科科治疗的骨质疏松症治疗期间诊断为MRONJ的患者。我们检查了随后的骨质疏松管理计划、骨折事件和骨密度(BMD)。结果:纳入36例患者(平均年龄78.5岁;94.4%的女性)。MRONJ的估计患病率为0.26%。所有患者均暴露于双膦酸盐,其中7例在MRONJ之前也接受了denosumab。在MRONJ后,只有14人继续接受抗骨质疏松治疗,这一决定受到MRONJ发作时较高骨折概率的影响。最常见的方案是特立帕肽-雷洛昔芬序列(n=8): 3例患者达到稳定的骨密度,4例达到改善的骨密度,1例表现出混合反应。患有混合BMD反应的患者也接受了denosumab治疗。6例患者在MRONJ后发生偶发性骨折,这些患者的BMD t评分低于对照组。2例患者出现MRONJ复发,这与MRONJ术后恢复双膦酸盐或地诺单抗治疗有关。这些患者的BMD t评分高于没有MRONJ复发的患者。结论:MRONJ具有挑战性,因为高骨折风险需要停用抗吸收药物。特立帕肽加雷洛昔芬可能是一个合理的方案。在MRONJ术后的骨质疏松管理中,需要个性化的决策来平衡骨折风险的降低和MRONJ复发的最小化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Osteoporosis Management after the Occurrence of Medication-Related Osteonecrosis of the Jaw: A 13-Year Experience at a Tertiary Center.

Background: We investigated osteoporosis management strategies and clinical outcomes following the occurrence of medicationrelated osteonecrosis of the jaw (MRONJ).

Methods: We retrospectively studied individuals diagnosed with MRONJ during osteoporosis treatment who were managed in the Osteoporosis Center or the Oral Maxillofacial Surgery & Dental Unit at Queen Mary Hospital in Hong Kong between 2010 and 2022. We examined subsequent osteoporosis management plans, fracture events, and bone mineral density (BMD).

Results: Thirty-six individuals were included (mean age, 78.5 years; 94.4% women). The estimated prevalence of MRONJ was 0.26%. All patients had been exposed to bisphosphonates, and seven had also received denosumab before MRONJ. Following MRONJ, only 14 individuals continued anti-osteoporosis treatment, a decision influenced by a higher fracture probability at MRONJ onset. The most common regimen was a teriparatide-raloxifene sequence (n=8): three patients achieved stable BMD, four achieved improving BMD, and one exhibited a mixed response. The patient with a mixed BMD response had also been treated with denosumab. Six patients sustained incident fractures after MRONJ, and these patients had lower BMD T-scores than their counterparts. Two patients experienced MRONJ recurrence, which was associated with the resumption of bisphosphonate or denosumab therapy after MRONJ. These patients had higher BMD T-scores than those who did not experience MRONJ recurrence.

Conclusion: MRONJ is challenging because high fracture risk necessitates discontinuation of antiresorptive agents. Teriparatide followed by raloxifene may be a reasonable regimen. Individualised decisions in osteoporosis management after MRONJ are required to balance fracture risk reduction with minimising MRONJ recurrence.

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