The 2024 Australian National Osteoporosis Guidelines in Postmenopausal Women and Men Aged Over 50 Years: A Comparative Perspective Within the Asia–Pacific Region

IF 2.4 4区 医学 Q2 RHEUMATOLOGY
Alwin Lian, Manju Chandran, Peter K. K. Wong
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This editorial explores Australia's recently released Osteoporosis Guidelines in the context of other Asia–Pacific recommendations, highlighting key similarities and differences in screening, risk assessment and treatment (Table 1).</p><p>The Royal Australian College of General Practitioners and Healthy Bones Australia published national guidelines for osteoporosis management in postmenopausal women and men aged ≥ 50 years in 2024 [<span>2, 3</span>]. Representative Asia–Pacific guidelines published in English chosen were the 2024 Osteoporosis Society of Hong Kong (HK) Guideline for Clinical Management of Postmenopausal Osteoporosis [<span>5</span>], the 2024 Guidelines for Osteoporosis—Korean Society of Menopause [<span>4</span>], the 2021 Indian Society for Bone and Mineral Research Position Statement for the Diagnosis and Treatment of Osteoporosis in Adults [<span>6</span>], the 2021 Clinical Standards for Fracture Liaison Services in New Zealand (NZ) [<span>9</span>] with the 2017 Guidance on the Diagnosis and Management of Osteoporosis in NZ [<span>7</span>], the 2018 Singaporean Appropriate Care Guide for Osteoporosis Identification and Management in Primary Care [<span>8</span>], and the 2021 Summary of the Thai Osteoporosis Foundation Clinical Practice Guidelines on the Diagnosis and Management of Osteoporosis [<span>10</span>]. (Of note, the Chinese guidelines were published in Mandarin and so not included in this Editorial [<span>11</span>].) Like the Australian guideline, the Thai document targeted postmenopausal women and men aged ≥ 50 years [<span>10</span>]. There was some variability in target population of the other guidelines, for example, the HK and Korean guidelines were directed as postmenopausal women [<span>4, 5</span>] and the Singaporean guideline targeted postmenopausal women and men aged ≥ 65 years [<span>8</span>]. Despite this, the principles discussed in the various guidelines were similar. It is not our intention to identify which guideline might be “better” as each document was written by local experts cognisant of the limitations and vagaries of their particular national healthcare system, funding envelope and at-risk population. There are obviously significant differences in national healthcare resources. This is particularly highlighted in the Indian guideline which was drafted specifically for a resource-constrained healthcare environment with a large at-risk population [<span>6</span>].</p><p>Although some countries have adopted age-based thresholds for bone health assessment, others prioritize risk-based approaches using the Fracture Risk Assessment Tool (FRAX) or other algorithms. This reflects the need for adaptable strategies that align with local healthcare priorities and funding. Australian guidelines recommend referral for bone density assessment by dual energy x-ray absorptiometry (DXA) in everyone ≥ 50 years of age with (i) a minimal trauma fracture (MTF), or (ii) in those without a fracture, who have risk factors for osteoporosis and a FRAX risk for major osteoporotic fracture (MOF) ≥ 10% [<span>2</span>]. None of the three large population-based randomized controlled trials (RCTs) of screening in women for prevention of osteoporotic fractures showed a reduction in the primary outcome of all fractures [<span>12-14</span>]. However, a significant reduction in hip fracture was found in a meta-analysis of these trials (<i>n</i> &gt; 42 000 in total), with an absolute risk reduction of 0.47% over 5 years of treatment [<span>15</span>]. Due to inadequately defined Australian thresholds of absolute fracture risk and lack of data on screening in men, insufficient evidence was available to support a population-based-screening program in Australia [<span>2</span>].</p><p>This is mirrored in NZ where the presence of fragility fractures or osteoporosis risk factors directs case finding [<span>7</span>]. However, in HK [<span>5</span>], India [<span>6</span>], Korea [<span>4</span>], and Thailand, screening is based on age and risk factors. Ages for screening are men ≥ 70 years and women ≥ 65 years in HK [<span>5</span>] and Thailand [<span>10</span>], men ≥ 65 years and women ≥ 60 years in India [<span>6</span>], and women ≥ 65 years in Korea [<span>4</span>]. Singaporean guidelines suggest use of the Osteoporosis Self-Assessment Tool for Asians to inform the need for DXA assessment [<span>8</span>].</p><p>All the above guidelines recommend the use of FRAX (https://fraxplus.org) for absolute fracture risk assessment. However, in HK, a local alternative, such as the Chinese Osteoporosis Screening Algorithm (COSA) [<span>5</span>] may be appropriate, and NZ guidelines suggest either FRAX or the Garvan Fracture Risk Calculator (https://www.garvan.org.au/research/bone-fracture-risk-calculator) [<span>7</span>]. The Australian document suggests the latter may be of particular use in those at high falls risk, as this is not an input criterion for the current FRAX model [<span>2</span>]. Ongoing local validation studies are required to further refine the predictive value of fracture risk assessment tools.</p><p>Identification of patients at “very high” or “high” fracture risk is an evolving important concept allowing risk stratification for earlier access to bone anabolic agents. However, there is currently no internationally recognized definition for this. The 2024 Australian guidelines define very high fracture risk as a T-score ≤ −3.0 and fracture within 2 years, and/or (i) history of ≥ 2 fragility fractures, and/or (ii) presence of clinical risk factors, such as corticosteroid use, low body mass index (BMI), or recurrent falls, and/or (iii) a MOF FRAX risk of ≥ 30%, or hip fracture risk of ≥ 4.5% [<span>2</span>].</p><p>The HK guideline is broadly similar, substituting FRAX risk criteria for fractures sustained on anti-resorptive therapy [<span>5</span>]. The Thai guidelines define very high fracture risk as either (i) fragility hip or vertebral fracture within 12 months in individuals ≥ 65 years and T-score ≤ −2.5, or (ii) recurrent vertebral fracture or vertebral fractures at ≥ 2 levels with moderate-to-severe deformity, or (iii) bilateral hip fractures, hip and vertebral fractures, or multiple fractures (≥ 3 times, or ≥ 3 sites), (iv) T-score &lt; −3.5 in men ≥ 70 years or women ≥ 65 years, or (v) fragility fracture after ≥ 2 years of bone protective therapy [<span>10</span>]. The Indian guidelines identify a fracture within 2 years as a marker for very high fracture risk [<span>6</span>] while the NZ, Singaporean and Korean guidelines do not specify a definition [<span>4, 7, 8</span>].</p><p>As this is an evolving concept, it is not surprising that heterogeneity in definition exists between countries—especially as there are funding differences for access to bone anabolic agents.</p><p>Although treatment thresholds are generally aligned across the Asia–Pacific Region, with the usual caveats about individualized clinical judgment, therapy initiation is guided by fracture risk and healthcare system factors. The Australian guidelines recommend initiation of bone protective pharmacological therapy in individuals with (i) very high fracture risk, or (ii) minimal trauma hip or vertebral fracture, or (iii) MTF at other sites and a T-score of ≤ −1.5 [<span>2</span>]. It further recommends treatment in individuals with risk factors, but no fracture with either a T-score of ≤ −2.5, or a T-score between −1.5 and-2.5 and a FRAX MOF risk of ≥ 20%, or hip fracture risk of ≥ 3%. The Indian guidelines note that these FRAX thresholds may underestimate fracture risk in Indians, and studies are underway to better inform local clinical practice [<span>6</span>]. Thai guidelines recommend treatment in the presence of a fragility vertebral or hip fracture, T-score of ≤ −2.5 or a T-score between −1.0 and −2.5 and a FRAX hip fracture risk of ≥ 3%, but also a T-score between −1.0 and −2.5 and a fragility fracture of the proximal humerus, pelvis, or distal forearm [<span>10</span>].</p><p>Access to osteoanabolic therapy is influenced by national healthcare policies and funding. Recent expansion of romosozumab access in Australia is a positive step and similar discussions are occurring in other parts of the Asia–Pacific Region. The Australian guidelines recommend consideration of bone anabolic agents (romosozumab or teriparatide) for those at very high fracture risk (see definition above). Until recently, this was only subsidized under the national Pharmaceutical Benefits Scheme for second-line therapy following fracture while on anti-resorptive therapy with a T-score ≤ −3.0 [<span>2</span>]. However, as of November 2024, romosozumab is available “first-line” for those with a T-score ≤ −2.5 with a symptomatic MTF and either ≥ 1 hip or symptomatic vertebral fracture in the previous 24 months, or a history of ≥ 2 fractures, including 1 symptomatic new fracture in the previous 24 months [<span>16</span>].</p><p>Early bone anabolic agent use for those at very high fracture risk is recommended in the HK and Thai guidelines [<span>5, 10</span>]. The Indian guidelines recommend teriparatide as first-line therapy in individuals with either vertebral fractures or very high fracture risk and intravenous zoledronic acid in hip fracture patients—preferably prior to hospital discharge [<span>6</span>]. The NZ guidelines recommend bisphosphonates as first-line therapy—although these were drafted prior to widespread use of bone anabolic therapy [<span>7</span>]. The Korean guidelines make no specific recommendation on the choice of bone protective therapy while the Singaporean guidelines make no demarcation between first and second-line therapies [<span>4, 8</span>].</p><p>Although exercise is widely recognized as a key component of osteoporosis management, widespread implementation and adherence to exercise regimes remain problematic. The Australian guidelines discuss the role of exercise for increasing or maintaining bone mass, for promotion of balance and falls prevention, and for fracture reduction [<span>2</span>]. Moderate-to-high-impact weight-bearing activities (jumping, hopping) and progressive resistance (strength) training are most effective for increasing or maintaining BMD, while there is minimal evidence of benefit for low-intensity resistance or low-impact weight-bearing aerobic exercises, such as walking and cycling [<span>17, 18</span>]. The role of the healthcare professional in adopting an encouraging approach to exercise is highlighted. The HK and Singaporean guidelines discuss falls prevention and the benefit of Tai-chi in balance training [<span>5, 8</span>], while the Korean guidelines discuss the importance of exercise on bone health, including exercises to avoid [<span>4</span>]. New Zealand guidelines mention 30 min of weight-bearing exercise per day [<span>7</span>], while the Thai and Indian guidelines do not specifically explore the role of exercise in bone protection [<span>6, 10</span>].</p><p>A Fracture Liaison Service (FLS) identifies and coordinates care for patients with a fragility fracture to reduce the risk of a subsequent fracture and is the most effective and cost-effective system-wide model of care to prevent refracture [<span>19</span>]. While there is widespread agreement regarding its importance, there are many barriers to widespread implementation—especially cost. Even in a relatively wealthy country like Australia, only New South Wales has a system-wide osteoporosis refracture program built around FLSs [<span>2</span>]. There has been widespread acceptance of this model of care in HK and NZ [<span>4, 9</span>]. Although FLSs are present in India [<span>20</span>], Thailand [<span>21</span>], and Singapore [<span>22</span>], there are no specific recommendations for widespread implementation in the relevant guidelines [<span>4, 6, 8, 10</span>]. Collaboration between countries may help optimize FLS models for broader adoption throughout the region.</p><p>The Asia–Pacific Region encompasses culturally and ethnically diverse populations with variations in healthcare resources, leading to heterogeneity in osteoporosis guidelines. A major reason for differences in recommendations is variation in the cost of osteoporosis medications and variable coverage of investigation and treatment costs by national healthcare systems. Australia, with a large migrant population, is a microcosm of the region at large, and dialogue, collaboration, and knowledge exchange with Asia–Pacific partners is important to produce guidelines representative of this diversity. The Asia–Pacific Consortium on Osteoporosis Framework was developed to establish clinical standards for osteoporosis management across the Region and is an important step toward harmonizing best practice [<span>23</span>]. As many countries refine osteoporosis management strategies, aligning national guidelines with evidence-based regional frameworks will drive more consistent and equitable osteoporosis care across the Asia–Pacific Region.</p><p>The initial draft was written by A.L. and P.K.K.W. All authors contributed to manuscript review.</p><p>Peter K. K. Wong is Honorary Medical Director and Board Member, Healthy Bones Australia, and an Associate Editor of the <i>Journal</i>. Manju Chandran has previously received travel grants and honoraria from Amgen Asia and Promedius AI solutions for speaking and chairing. Alwin Lian declares no relevant conflicts of interest.</p>","PeriodicalId":14330,"journal":{"name":"International Journal of Rheumatic Diseases","volume":"28 4","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1756-185X.70220","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Rheumatic Diseases","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1756-185X.70220","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
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Abstract

Osteoporosis is a major public challenge in the Asia–Pacific region where it affects ≤ 30% of women aged ≥ 40 years and ≤ 10% of men in developed economies [1]. Although many national guidelines within the Asia–Pacific region offer tailored strategies, differences in screening, risk assessment and treatment thresholds highlight the need for stronger, evidence-driven strategies to optimize patient outcomes and the importance of regional dialogue and knowledge exchange. This editorial explores Australia's recently released Osteoporosis Guidelines in the context of other Asia–Pacific recommendations, highlighting key similarities and differences in screening, risk assessment and treatment (Table 1).

The Royal Australian College of General Practitioners and Healthy Bones Australia published national guidelines for osteoporosis management in postmenopausal women and men aged ≥ 50 years in 2024 [2, 3]. Representative Asia–Pacific guidelines published in English chosen were the 2024 Osteoporosis Society of Hong Kong (HK) Guideline for Clinical Management of Postmenopausal Osteoporosis [5], the 2024 Guidelines for Osteoporosis—Korean Society of Menopause [4], the 2021 Indian Society for Bone and Mineral Research Position Statement for the Diagnosis and Treatment of Osteoporosis in Adults [6], the 2021 Clinical Standards for Fracture Liaison Services in New Zealand (NZ) [9] with the 2017 Guidance on the Diagnosis and Management of Osteoporosis in NZ [7], the 2018 Singaporean Appropriate Care Guide for Osteoporosis Identification and Management in Primary Care [8], and the 2021 Summary of the Thai Osteoporosis Foundation Clinical Practice Guidelines on the Diagnosis and Management of Osteoporosis [10]. (Of note, the Chinese guidelines were published in Mandarin and so not included in this Editorial [11].) Like the Australian guideline, the Thai document targeted postmenopausal women and men aged ≥ 50 years [10]. There was some variability in target population of the other guidelines, for example, the HK and Korean guidelines were directed as postmenopausal women [4, 5] and the Singaporean guideline targeted postmenopausal women and men aged ≥ 65 years [8]. Despite this, the principles discussed in the various guidelines were similar. It is not our intention to identify which guideline might be “better” as each document was written by local experts cognisant of the limitations and vagaries of their particular national healthcare system, funding envelope and at-risk population. There are obviously significant differences in national healthcare resources. This is particularly highlighted in the Indian guideline which was drafted specifically for a resource-constrained healthcare environment with a large at-risk population [6].

Although some countries have adopted age-based thresholds for bone health assessment, others prioritize risk-based approaches using the Fracture Risk Assessment Tool (FRAX) or other algorithms. This reflects the need for adaptable strategies that align with local healthcare priorities and funding. Australian guidelines recommend referral for bone density assessment by dual energy x-ray absorptiometry (DXA) in everyone ≥ 50 years of age with (i) a minimal trauma fracture (MTF), or (ii) in those without a fracture, who have risk factors for osteoporosis and a FRAX risk for major osteoporotic fracture (MOF) ≥ 10% [2]. None of the three large population-based randomized controlled trials (RCTs) of screening in women for prevention of osteoporotic fractures showed a reduction in the primary outcome of all fractures [12-14]. However, a significant reduction in hip fracture was found in a meta-analysis of these trials (n > 42 000 in total), with an absolute risk reduction of 0.47% over 5 years of treatment [15]. Due to inadequately defined Australian thresholds of absolute fracture risk and lack of data on screening in men, insufficient evidence was available to support a population-based-screening program in Australia [2].

This is mirrored in NZ where the presence of fragility fractures or osteoporosis risk factors directs case finding [7]. However, in HK [5], India [6], Korea [4], and Thailand, screening is based on age and risk factors. Ages for screening are men ≥ 70 years and women ≥ 65 years in HK [5] and Thailand [10], men ≥ 65 years and women ≥ 60 years in India [6], and women ≥ 65 years in Korea [4]. Singaporean guidelines suggest use of the Osteoporosis Self-Assessment Tool for Asians to inform the need for DXA assessment [8].

All the above guidelines recommend the use of FRAX (https://fraxplus.org) for absolute fracture risk assessment. However, in HK, a local alternative, such as the Chinese Osteoporosis Screening Algorithm (COSA) [5] may be appropriate, and NZ guidelines suggest either FRAX or the Garvan Fracture Risk Calculator (https://www.garvan.org.au/research/bone-fracture-risk-calculator) [7]. The Australian document suggests the latter may be of particular use in those at high falls risk, as this is not an input criterion for the current FRAX model [2]. Ongoing local validation studies are required to further refine the predictive value of fracture risk assessment tools.

Identification of patients at “very high” or “high” fracture risk is an evolving important concept allowing risk stratification for earlier access to bone anabolic agents. However, there is currently no internationally recognized definition for this. The 2024 Australian guidelines define very high fracture risk as a T-score ≤ −3.0 and fracture within 2 years, and/or (i) history of ≥ 2 fragility fractures, and/or (ii) presence of clinical risk factors, such as corticosteroid use, low body mass index (BMI), or recurrent falls, and/or (iii) a MOF FRAX risk of ≥ 30%, or hip fracture risk of ≥ 4.5% [2].

The HK guideline is broadly similar, substituting FRAX risk criteria for fractures sustained on anti-resorptive therapy [5]. The Thai guidelines define very high fracture risk as either (i) fragility hip or vertebral fracture within 12 months in individuals ≥ 65 years and T-score ≤ −2.5, or (ii) recurrent vertebral fracture or vertebral fractures at ≥ 2 levels with moderate-to-severe deformity, or (iii) bilateral hip fractures, hip and vertebral fractures, or multiple fractures (≥ 3 times, or ≥ 3 sites), (iv) T-score < −3.5 in men ≥ 70 years or women ≥ 65 years, or (v) fragility fracture after ≥ 2 years of bone protective therapy [10]. The Indian guidelines identify a fracture within 2 years as a marker for very high fracture risk [6] while the NZ, Singaporean and Korean guidelines do not specify a definition [4, 7, 8].

As this is an evolving concept, it is not surprising that heterogeneity in definition exists between countries—especially as there are funding differences for access to bone anabolic agents.

Although treatment thresholds are generally aligned across the Asia–Pacific Region, with the usual caveats about individualized clinical judgment, therapy initiation is guided by fracture risk and healthcare system factors. The Australian guidelines recommend initiation of bone protective pharmacological therapy in individuals with (i) very high fracture risk, or (ii) minimal trauma hip or vertebral fracture, or (iii) MTF at other sites and a T-score of ≤ −1.5 [2]. It further recommends treatment in individuals with risk factors, but no fracture with either a T-score of ≤ −2.5, or a T-score between −1.5 and-2.5 and a FRAX MOF risk of ≥ 20%, or hip fracture risk of ≥ 3%. The Indian guidelines note that these FRAX thresholds may underestimate fracture risk in Indians, and studies are underway to better inform local clinical practice [6]. Thai guidelines recommend treatment in the presence of a fragility vertebral or hip fracture, T-score of ≤ −2.5 or a T-score between −1.0 and −2.5 and a FRAX hip fracture risk of ≥ 3%, but also a T-score between −1.0 and −2.5 and a fragility fracture of the proximal humerus, pelvis, or distal forearm [10].

Access to osteoanabolic therapy is influenced by national healthcare policies and funding. Recent expansion of romosozumab access in Australia is a positive step and similar discussions are occurring in other parts of the Asia–Pacific Region. The Australian guidelines recommend consideration of bone anabolic agents (romosozumab or teriparatide) for those at very high fracture risk (see definition above). Until recently, this was only subsidized under the national Pharmaceutical Benefits Scheme for second-line therapy following fracture while on anti-resorptive therapy with a T-score ≤ −3.0 [2]. However, as of November 2024, romosozumab is available “first-line” for those with a T-score ≤ −2.5 with a symptomatic MTF and either ≥ 1 hip or symptomatic vertebral fracture in the previous 24 months, or a history of ≥ 2 fractures, including 1 symptomatic new fracture in the previous 24 months [16].

Early bone anabolic agent use for those at very high fracture risk is recommended in the HK and Thai guidelines [5, 10]. The Indian guidelines recommend teriparatide as first-line therapy in individuals with either vertebral fractures or very high fracture risk and intravenous zoledronic acid in hip fracture patients—preferably prior to hospital discharge [6]. The NZ guidelines recommend bisphosphonates as first-line therapy—although these were drafted prior to widespread use of bone anabolic therapy [7]. The Korean guidelines make no specific recommendation on the choice of bone protective therapy while the Singaporean guidelines make no demarcation between first and second-line therapies [4, 8].

Although exercise is widely recognized as a key component of osteoporosis management, widespread implementation and adherence to exercise regimes remain problematic. The Australian guidelines discuss the role of exercise for increasing or maintaining bone mass, for promotion of balance and falls prevention, and for fracture reduction [2]. Moderate-to-high-impact weight-bearing activities (jumping, hopping) and progressive resistance (strength) training are most effective for increasing or maintaining BMD, while there is minimal evidence of benefit for low-intensity resistance or low-impact weight-bearing aerobic exercises, such as walking and cycling [17, 18]. The role of the healthcare professional in adopting an encouraging approach to exercise is highlighted. The HK and Singaporean guidelines discuss falls prevention and the benefit of Tai-chi in balance training [5, 8], while the Korean guidelines discuss the importance of exercise on bone health, including exercises to avoid [4]. New Zealand guidelines mention 30 min of weight-bearing exercise per day [7], while the Thai and Indian guidelines do not specifically explore the role of exercise in bone protection [6, 10].

A Fracture Liaison Service (FLS) identifies and coordinates care for patients with a fragility fracture to reduce the risk of a subsequent fracture and is the most effective and cost-effective system-wide model of care to prevent refracture [19]. While there is widespread agreement regarding its importance, there are many barriers to widespread implementation—especially cost. Even in a relatively wealthy country like Australia, only New South Wales has a system-wide osteoporosis refracture program built around FLSs [2]. There has been widespread acceptance of this model of care in HK and NZ [4, 9]. Although FLSs are present in India [20], Thailand [21], and Singapore [22], there are no specific recommendations for widespread implementation in the relevant guidelines [4, 6, 8, 10]. Collaboration between countries may help optimize FLS models for broader adoption throughout the region.

The Asia–Pacific Region encompasses culturally and ethnically diverse populations with variations in healthcare resources, leading to heterogeneity in osteoporosis guidelines. A major reason for differences in recommendations is variation in the cost of osteoporosis medications and variable coverage of investigation and treatment costs by national healthcare systems. Australia, with a large migrant population, is a microcosm of the region at large, and dialogue, collaboration, and knowledge exchange with Asia–Pacific partners is important to produce guidelines representative of this diversity. The Asia–Pacific Consortium on Osteoporosis Framework was developed to establish clinical standards for osteoporosis management across the Region and is an important step toward harmonizing best practice [23]. As many countries refine osteoporosis management strategies, aligning national guidelines with evidence-based regional frameworks will drive more consistent and equitable osteoporosis care across the Asia–Pacific Region.

The initial draft was written by A.L. and P.K.K.W. All authors contributed to manuscript review.

Peter K. K. Wong is Honorary Medical Director and Board Member, Healthy Bones Australia, and an Associate Editor of the Journal. Manju Chandran has previously received travel grants and honoraria from Amgen Asia and Promedius AI solutions for speaking and chairing. Alwin Lian declares no relevant conflicts of interest.

2024年澳大利亚50岁以上绝经后女性和男性骨质疏松症指南:亚太地区的比较视角
骨质疏松症是亚太地区的一项重大公共挑战,在发达经济体中,骨质疏松症影响着≤30%≥40岁的女性和≤10%的男性。尽管亚太地区的许多国家指南提供了量身定制的战略,但筛查、风险评估和治疗阈值的差异突出表明,需要制定更强有力的循证战略,以优化患者结果,并强调区域对话和知识交流的重要性。这篇社论探讨了澳大利亚最近发布的骨质疏松症指南与其他亚太地区建议的背景,突出了筛查、风险评估和治疗方面的关键异同(表1)。澳大利亚皇家全科医师学院和澳大利亚健康骨骼学院于2024年发布了绝经后50岁以上男女骨质疏松症管理国家指南[2,3]。入选的亚太地区代表性英文指南有《2024年香港骨质疏松学会(HK)绝经后骨质疏松临床管理指南[5]》、《2024年骨质疏松指南-韩国绝经学会指南[5]》、《2021年印度骨与矿物研究学会成人骨质疏松诊断与治疗立场声明[6]》、2021年新西兰骨折联络服务临床标准[9]与2017年新西兰骨质疏松症诊断和管理指南[7],2018年新加坡初级保健骨质疏松症识别和管理适当护理指南[8],以及2021年泰国骨质疏松症基金会骨质疏松症诊断和管理临床实践指南摘要bbb。(值得注意的是,中国的指南是用中文发布的,因此没有包括在本社论中。)与澳大利亚的指南一样,泰国的指南针对的是年龄≥50岁的绝经后女性和男性。其他指南的目标人群存在一些差异,例如,香港和韩国指南针对的是绝经后妇女[4,5],新加坡指南针对的是年龄≥65岁的绝经后妇女和男性[10]。尽管如此,各种指导方针中讨论的原则是相似的。我们不打算确定哪一份指南可能“更好”,因为每一份文件都是由当地专家撰写的,他们认识到本国医疗体系、资金范围和风险人群的局限性和变幻莫测。各国医疗资源存在显著差异。印度指南特别强调了这一点,该指南是专门为资源有限的医疗保健环境和大量高危人口起草的。尽管一些国家采用了基于年龄的骨健康评估阈值,但其他国家优先考虑使用骨折风险评估工具(FRAX)或其他算法的基于风险的方法。这反映出需要制定适应当地卫生保健优先事项和资金的适应性战略。澳大利亚指南建议,对于年龄≥50岁、(i)轻度创伤性骨折(MTF)或(ii)无骨折、有骨质疏松危险因素和严重骨质疏松性骨折(MOF) FRAX风险≥10%的患者,推荐采用双能x线吸收仪(DXA)进行骨密度评估。三项基于人群的女性骨质疏松性骨折筛查的随机对照试验(RCTs)均未显示所有骨折的主要结局都有所降低[12-14]。然而,在对这些试验的荟萃分析中发现,髋部骨折发生率显著降低(总共42000例),治疗5年的绝对风险降低0.47%。由于澳大利亚对绝对骨折风险的阈值定义不充分,并且缺乏男性筛查的数据,因此没有足够的证据支持在澳大利亚开展以人群为基础的筛查项目[10]。新西兰的情况也是如此,脆性骨折或骨质疏松风险因素的存在直接影响了病例的发现。然而,在香港[5]、印度[6]、韩国[5]和泰国,筛查是基于年龄和风险因素。筛查年龄:香港[5]和泰国[10]男性≥70岁,女性≥65岁;印度[6]男性≥65岁,女性≥60岁;韩国[4]女性≥65岁。新加坡指南建议使用亚洲人骨质疏松自我评估工具来告知DXA评估的必要性。以上所有指南都推荐使用FRAX (https://fraxplus.org)进行绝对骨折风险评估。然而,在香港,当地的替代方案,如中国骨质疏松症筛查算法(COSA)[5]可能是合适的,新西兰指南建议FRAX或Garvan骨折风险计算器(https://www.garvan.org.au/research/bone-fracture-risk-calculator)[7]。 澳大利亚的文件表明,后者可能特别适用于那些有高跌倒风险的人,因为这不是当前FRAX模型的输入标准。为了进一步完善压裂风险评估工具的预测价值,需要进行持续的局部验证研究。识别“非常高”或“高”骨折风险的患者是一个不断发展的重要概念,允许早期获得骨合成代谢药物的风险分层。然而,目前还没有国际公认的定义。2024年澳大利亚指南将极高骨折风险定义为t评分≤- 3.0,2年内骨折,和/或(i)≥2次脆性骨折史,和/或(ii)存在临床危险因素,如皮质类固醇使用、低体重指数(BMI)或复发跌倒,和/或(iii) MOF FRAX风险≥30%,或髋部骨折风险≥4.5%。HK指南大致相似,用FRAX风险标准代替了抗吸收治疗后骨折的风险标准。泰国指南将极高骨折风险定义为(i)≥65岁且t评分≤- 2.5的个体在12个月内发生脆性髋部或椎体骨折,或(ii)复发性椎体骨折或椎体骨折≥2个级别,伴有中度至重度畸形,或(iii)双侧髋部骨折、髋部和椎体骨折或多发骨折(≥3次或≥3个部位),(iv)≥70岁或≥65岁的男性t评分为&lt; - 3.5。(v)骨保护治疗≥2年后发生脆性骨折[10]。印度的指南将2年内发生骨折作为非常高骨折风险的标志,而新西兰、新加坡和韩国的指南没有明确定义[4,7,8]。由于这是一个不断发展的概念,各国之间在定义上存在差异并不奇怪,特别是在获得骨合成代谢剂的资金方面存在差异。尽管整个亚太地区的治疗阈值通常是一致的,但通常有个体化临床判断的警告,治疗开始是由骨折风险和医疗保健系统因素指导的。澳大利亚指南建议对以下人群开始骨保护药物治疗:(i)非常高的骨折风险,或(ii)极小的髋部或椎体骨折创伤,或(iii)其他部位MTF, t评分≤- 1.5[2]。它进一步建议对有危险因素的个体进行治疗,但没有骨折,t评分≤-2.5,或t评分在- 1.5 -2.5之间,FRAX MOF风险≥20%,或髋部骨折风险≥3%。印度指南指出,这些FRAX阈值可能低估了印度人的骨折风险,目前正在进行研究,以更好地为当地临床实践提供信息。泰国指南建议治疗脆性椎体或髋部骨折,t评分≤- 2.5或t评分在- 1.0至- 2.5之间,FRAX髋部骨折风险≥3%,但t评分在- 1.0至- 2.5之间,肱骨近端、骨盆或前臂远端脆性骨折。获得骨合成代谢治疗受到国家卫生保健政策和资金的影响。最近romosozumab在澳大利亚获得的扩大是一个积极的步骤,类似的讨论正在亚太地区的其他地区进行。澳大利亚指南建议对骨折风险极高的患者考虑骨合成代谢药物(romosozumab或teriparatide)(见上文定义)。直到最近,只有在t评分≤- 3.0[2]的抗吸收治疗中,骨折后的二线治疗才得到国家药品福利计划的补贴。然而,截至2024年11月,romosozumab可用于t评分≤- 2.5的症状性MTF患者,并且在过去24个月内有≥1例髋关节或症状性椎体骨折,或有≥2例骨折史,包括在过去24个月内有1例新的症状性骨折。在香港和泰国的指南中,建议对骨折风险非常高的患者早期使用骨合成代谢剂[5,10]。印度指南推荐特立帕肽作为椎体骨折或非常高骨折风险患者的一线治疗,推荐髋部骨折患者静脉注射唑来膦酸——最好在出院前使用。新西兰指南推荐双膦酸盐作为一线治疗,尽管这些指南是在骨合成代谢疗法bbb广泛使用之前起草的。韩国指南对骨保护治疗的选择没有具体推荐,新加坡指南对一线和二线治疗没有区分[4,8]。虽然运动被广泛认为是骨质疏松症管理的关键组成部分,但广泛实施和坚持运动制度仍然存在问题。 澳大利亚指南讨论了运动在增加或维持骨量、促进平衡、预防跌倒和减少骨折方面的作用。中到高强度负重活动(跳跃、跳跃)和进行性阻力(力量)训练对于增加或维持骨密度最有效,而低强度阻力或低强度负重有氧运动(如步行和骑自行车)的益处证据很少[17,18]。强调了保健专业人员在采用鼓励方法进行锻炼方面的作用。香港和新加坡的指南讨论了预防跌倒和太极拳在平衡训练中的益处[5,8],而韩国的指南讨论了运动对骨骼健康的重要性,包括避免[4]的运动。新西兰的指南提到了每天30分钟的负重运动,而泰国和印度的指南并没有具体探讨运动在骨骼保护中的作用[6,10]。骨折联络服务(FLS)识别和协调脆性骨折患者的护理,以降低后续骨折的风险,是预防再骨折的最有效和最具成本效益的全系统护理模式。虽然人们对其重要性达成了广泛的共识,但广泛实施仍存在许多障碍——尤其是成本。即使在澳大利亚这样一个相对富裕的国家,也只有新南威尔士州有一个围绕FLSs的系统性骨质疏松症再骨折项目。在香港和新西兰,这种护理模式已被广泛接受[4,9]。虽然FLSs存在于印度b[20]、泰国b[21]和新加坡b[22],但相关指南中没有关于广泛实施FLSs的具体建议[4,6,8,10]。各国之间的合作可能有助于优化FLS模式,以便在整个地区得到更广泛的采用。亚太地区包含文化和种族多样化的人口,医疗资源存在差异,导致骨质疏松症指南存在异质性。建议存在差异的一个主要原因是骨质疏松症药物的费用不同,以及国家卫生保健系统对调查和治疗费用的覆盖范围不同。拥有大量移民人口的澳大利亚是整个亚太地区的一个缩影,与亚太伙伴的对话、合作和知识交流对于制定代表这种多样性的指导方针至关重要。亚太骨质疏松症联盟框架的建立是为了建立整个地区骨质疏松症管理的临床标准,是朝着协调最佳实践迈出的重要一步。随着许多国家完善骨质疏松症管理战略,将国家指南与循证区域框架相结合将推动亚太地区骨质疏松症护理更加一致和公平。初稿由A.L.和P.K.K.W.撰写,所有作者都参与了手稿审查。Peter K. K. Wong是澳大利亚健康骨骼协会的名誉医学主任和董事会成员,也是该杂志的副主编。Manju Chandran此前曾获得安进亚洲和Promedius AI解决方案的旅行补助金和酬金,用于演讲和主持。Alwin Lian宣布没有相关利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
4.00%
发文量
362
审稿时长
1 months
期刊介绍: The International Journal of Rheumatic Diseases (formerly APLAR Journal of Rheumatology) is the official journal of the Asia Pacific League of Associations for Rheumatology. The Journal accepts original articles on clinical or experimental research pertinent to the rheumatic diseases, work on connective tissue diseases and other immune and allergic disorders. The acceptance criteria for all papers are the quality and originality of the research and its significance to our readership. Except where otherwise stated, manuscripts are peer reviewed by two anonymous reviewers and the Editor.
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