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Setting targets, measuring costs, tracking health outcomes and learning lessons 设定目标、衡量成本、跟踪健康成果并吸取经验教训。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-22 DOI: 10.5694/mja2.52474
Virginia Barbour
<p>This issue of the <i>MJA</i> has a range of articles that examine various aspects of the Australian health system, and which then reflect on the lessons that can be drawn. The articles cover a wide diversity of topics, from stroke targets to hospital-acquired complications, cost barriers to medication access and lessons learnt from the coronavirus disease 2019 (COVID-19) pandemic in remote Aboriginal and Torres Strait Islander communities.</p><p>A perspective by Kleinig and colleagues (https://doi.org/10.5694/mja2.52459) describes the 30/60/90 national stroke targets, which are that, by 2030 in Australia, median times for key interventions for stroke will be under 30, 60 or 90 minutes as appropriate (eg, national median endovascular clot retrieval door-to-puncture time < 30 minutes), and that certified stroke unit care will be provided to more than 90% of patients with primary stroke diagnosis. The authors note the need for a national commitment to meet these targets, and highlight that they are essential, given Australia's lagging position in both speed of treatment and admission to stroke units. Critically, the authors note that there is no need to reinvent the time saving strategies used elsewhere; rather, they need to be adapted to the Australian context.</p><p>In a research article, Ní Chróinín and colleagues (https://doi.org/10.5694/mja2.52462) assess the risk of hospital-acquired complications in people with dementia who were admitted to five public hospitals in the South Western Sydney Local Health District over an eleven-year period. They found that dementia was associated with higher risks of falls, pressure injury, delirium, and pneumonia. This article is an important quantification of risks that might be expected but where the size of the problem has not previously been clear; for example, it shows that patients with dementia were more than four times more likely to fall as matched individuals. It provides more evidence for the need for careful, person-centred care for these vulnerable individuals. In an editorial commenting on the research, Gordon and Hubbard (https://doi.org/10.5694/mja2.52463) noted that this article adds to the evidence of the risks for individuals with dementia, which is closely linked to frailty — itself a risk for hospital-acquired complications. What can be done to reduce these complications? Gordon and Hubbard emphasise the importance of hospital leadership in encouraging attitudes and behaviours that support patient safety, in addition to targeted person-centred interventions.</p><p>Costs of health care are increasingly important and can contribute substantially to cost of living pressures, now widespread across society. In a perspective, Ghinea (https://doi.org/10.5694/mja2.52427) discusses data on access to medication from the Australian Bureau of Statistics (ABS) 2022–23 Patient Experience Survey. They find that there are increasing cost barriers to access compared with previous years, with a dispro
"作者总结道:"这种由社区主导的方法突出了原住民在这一公共卫生应对措施以及其他公共卫生政策和倡议中发挥领导作用的重要性。"这不仅很好地提醒了我们需要做好数据收集工作,还提醒了我们必须结合实际情况应用这些数据,并确保在做出医疗保健决定时与受影响的个人和社区进行协商,以便在未来做出更好的决定。
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引用次数: 0
Towards national paediatric clinical practice guidelines 制定国家儿科临床实践指南。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-21 DOI: 10.5694/mja2.52501
Mike Starr

In reply: I thank Hill and colleagues1 for their interest in my article.2 The approach of the Australian Living Evidence Collaboration (ALEC) is impressive and one that guideline developers should aspire to. It is my understanding that the ALEC receives considerable funding from federal and state governments and several charitable foundations. In contrast, the Paediatric Improvement Collaborative (PIC) receives a fraction of ALEC's budget to produce clinical practice guidelines (CPGs). The “iron triangle” refers to the three key constraints that can affect a project.3 These are cost, time and quality. It is almost impossible to change one without affecting the others or damaging the quality of the overall project. The approach of PIC CPG development is based on evidence-based medicine (EBM), as described by Sackett and colleagues as the integration of clinical expertise with the best available clinical evidence from systematic research.4 There are almost 150 PIC CPGs available as point-of-care guidelines for clinicians caring for children, and between 30 and 40 new and updated CPGs are published each year. Within the constraints of the current resources, it is not feasible to use GRADE methods and maintain this output. The current PIC approach to the development of national paediatric CPGs prioritises EBM, collaboration and quality. Significant investment in infrastructure and capacity is required to sustain, and ideally, enhance the process.

No relevant disclosures.

回复:我感谢希尔及其同事1 对我文章的关注。2 澳大利亚生活证据合作组织(ALEC)的方法令人印象深刻,也是指南制定者应该学习的。据我所知,ALEC 从联邦政府、州政府和几个慈善基金会获得了大量资金。相比之下,儿科改进合作组织(PIC)用于制定临床实践指南(CPG)的预算仅为 ALEC 的一小部分。铁三角 "指的是可能影响项目的三个关键制约因素3 ,即成本、时间和质量。要改变其中一项而不影响其他几项或破坏整个项目的质量几乎是不可能的。PIC CPG 的开发方法以循证医学(EBM)为基础,正如 Sackett 及其同事所描述的那样,EBM 是将临床专业知识与来自系统研究的现有最佳临床证据相结合。在现有资源的限制下,使用 GRADE 方法并保持这种产出是不可行的。目前,太平洋岛屿国家(PIC)制定国家儿科 CPG 的方法将 EBM、合作和质量放在首位。需要对基础设施和能力进行大量投资,以维持并在理想情况下加强这一过程。
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引用次数: 0
Mental health-related hospitalisations of adolescents and their contact with child protection services to age 11 years, South Australia: a whole-of-population descriptive study 南澳大利亚州 11 岁以下青少年与精神健康相关的住院治疗及其与儿童保护服务机构的接触情况:全人口描述性研究。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-21 DOI: 10.5694/mja2.52489
Jessica Judd, Rhiannon M Pilkington, Catia Malvaso, Alexandra M Procter, Alicia Montgomerie, Jemma JA Anderson, Jon N Jureidini, Julie Petersen, John Lynch, Catherine R Chittleborough
<div> <section> <h3> Objectives</h3> <p>To investigate the number of mental health-related hospitalisations of adolescents (12–17 years) in South Australia by level of contact with the child protection system (0–11 years).</p> </section> <section> <h3> Study design</h3> <p>Whole-of-population descriptive study; analysis of de-identified linked administrative data from the Better Evidence Better Outcomes Linked Data (BEBOLD) platform.</p> </section> <section> <h3> Setting, participants</h3> <p>Adolescents born in South Australia, 1991–1999; linked SA Department for Child Protection, Admitted Patient Care (SA Health), and South Australian Perinatal Statistics collection (SA Department for Health and Wellbeing) data.</p> </section> <section> <h3> Main outcome measures</h3> <p>Proportion of adolescents (12–17 years) hospitalised with mental health-related diagnoses; proportion of mental health-related hospitalisations of adolescents, by level of child protection contact (0–11 years) (no contact, notification but not screened in, screened-in notification but not investigated, investigation but not substantiated, substantiation, and out-of-home care).</p> </section> <section> <h3> Results</h3> <p>Of 175 115 adolescents born during 1991–1999, 5646 (3.2%) had been hospitalised with mental health conditions, and 27 203 (15.5%) had histories of contact with child protection services. The proportion of adolescents admitted to hospital with mental health-related diagnoses increased with the level of prior child protection contact, from 3366 of 147 912 adolescents with no contact (2.3%), to 398 of 6645 with notifications (6.0%), to 209 of 1191 who had been placed in out-of-home care (17.5%). Contact with child protection services was recorded for 2280 of 5646 adolescents admitted to hospital with mental health-related diagnoses (40.4%); 4477 of 10 633 mental health-related hospitalisations (44.9%) were of adolescents with histories of child protection services contact, including 1285 hospitalisations (12.1%) of adolescents for whom substantiated maltreatment (but not out-of-home care) was recorded, and 568 hospitalisations (5.3%) of adolescents who had been placed in out-of-home care.</p> </section> <section> <h3> Conclusion</h3> <p>About 45% of mental health-related hospitalisations of 12–17-year-old adolescents were of people who had had contact with child pr
研究目的:调查南澳大利亚州青少年(12-17 岁)因精神疾病住院的人数:调查南澳大利亚州青少年(12-17 岁)因与儿童保护系统的接触程度(0-11 岁)而住院治疗的心理健康相关病例数量:全人群描述性研究;分析来自 "更好的证据更好的结果 "关联数据(BEBOLD)平台的去标识化关联管理数据:1991-1999年在南澳大利亚州出生的青少年;链接南澳大利亚州儿童保护部、入院病人护理部(南澳大利亚州卫生部)和南澳大利亚州围产期统计数据收集部(南澳大利亚州卫生和福利部)的数据:主要结果测量指标:青少年(12-17 岁)因精神健康相关诊断住院的比例;按儿童保护接触级别(0-11 岁)(未接触、通知但未筛查、筛查通知但未调查、调查但未证实、证实和家庭外护理)分列的青少年精神健康相关住院比例:在 1991-1999 年间出生的 175 115 名青少年中,有 5646 人(3.2%)曾因精神疾病住院治疗,27 203 人(15.5%)曾与儿童保护机构有过接触。因精神健康相关诊断而入院的青少年比例随着之前与儿童保护机构接触的程度而增加,从147 912名青少年中没有接触过儿童保护机构的3 366人(2.3%),到6645名青少年中接到通知的398人(6.0%),再到1191名青少年中被安置在家庭外照料的209人(17.5%)。在5646名被诊断为精神疾病的住院青少年中,有2280人(40.4%)曾与儿童保护机构有过接触;在10 633例与精神疾病有关的住院病例中,有4477人(44.9%)曾与儿童保护机构有过接触,其中包括1285例住院病例(12.1%),这些病例中的青少年曾被证实受到虐待(但未被安置在家庭外),还有568例住院病例(5.3%),这些青少年曾被安置在家庭外:结论:在 12-17 岁住院治疗的青少年中,约 45% 的人在 11 岁之前曾与儿童保护机构有过接触,而在所有青少年中,只有 15.5% 的人曾与儿童保护机构有过接触。与儿童保护史相关的创伤可能会带来长期的后遗症,因此在青少年因精神健康问题住院时应考虑到这一点。
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引用次数: 0
The association of child protection contact with mental health-related hospitalisations of adolescents, and their costs 儿童保护接触与青少年心理健康相关住院治疗的关联及其成本。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-21 DOI: 10.5694/mja2.52499
Paul Hotton
<p>Mental health challenges during adolescence are a critical public health concern, especially among young people at particular risk. The study reported by Judd and colleagues<span><sup>1</sup></span> in this issue of the <i>MJA</i> highlights the substantial mental health-related hospitalisation burden among adolescents aged 12–17 years who have had contact with child protection services. In their whole-of-population descriptive study, including 175 115 South Australian adolescents born during 1991–1999, they found that 44.9% of mental health-related hospitalisations were of young people with histories of child protection contact before the age of 11 years, despite only 15.5% of all adolescents having had such contact. Adolescents placed in out-of-home care as children were at particular risk. Strengths of the study include the use of comprehensive linked data; limitations include the non-inclusion of private hospitals data and the underestimation of the overall mental health-related burden by focusing solely on hospitalisations.<span><sup>1</sup></span> The study by Judd and colleagues helps highlight the implications and cost to the health care system of mental health problems among people who had contact with child protection and the importance of developing strength and long term resilience.</p><p>The link between child maltreatment and mental health problems is well established,<span><sup>2, 3</sup></span> and the impact of multiple forms of child maltreatment has recently been described.<span><sup>4</sup></span> Children who experience abuse and are removed from their families often struggle with mental health or behavioural challenges that make it harder to establish safe, secure, and trusting relationships, and they are at greater risk of mental health problems during adolescence, a key stage in emotional and social development. The trauma of abuse, combined with the instability of the child protection system, leads to complex mental health care needs.</p><p>The findings reported by Judd and her colleagues<span><sup>1</sup></span> support the view that adolescents who have had child protection contact, especially those placed in out-of-home care, are more frequently hospitalised because of their mental health problems than other adolescents.<span><sup>5</sup></span> In Australia, mental health care is divided between public and private systems, which leads to challenges and barriers with respect to access, waiting times, resources, and costs, further disadvantaging adolescents with histories of child protection contact.<span><sup>6</sup></span> Differences between services make navigating the health system complex, and available services may not adequately meet the needs of young people, especially if the services are not trauma-informed and culturally safe. The fragmentation of care between providers and sectors often leads to interruption of care and the loss of routine follow-up that could help manage emerging health problems.<span><
10 儿童保护系统中的青少年往往出身贫寒,多重压力导致他们心理健康状况不佳。总之,贾德及其同事1 的研究结果与其他研究结果相吻合,这些研究结果表明,我们亟需改革对曾接触过儿童保护服务的青少年的心理健康护理方式。通过提供早期、创伤知情干预以及解决健康的社会决定因素,我们可以减轻长期的心理健康负担,并减轻医疗保健系统的财政压力。不采取行动只会使创伤、不良心理健康和不断攀升的医疗成本循环往复。
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引用次数: 0
Towards national paediatric clinical practice guidelines 制定国家儿科临床实践指南。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-21 DOI: 10.5694/mja2.52500
Kelvin Hill, Steven McGloughlin, Sharon McGowan, Tari Turner

To the Editor: It is encouraging to hear the collaborative effort in paediatric clinical practice guidelines (CPGs).1 CPGs provide a critical tool for clinicians, health administrators and policy makers. We strongly agree that nationally coordinated efforts for evidence synthesis are clearly needed, which can be adapted if required. Starr1 also makes important points around suboptimal adherence to CPGs, including lack of currency and concerns on evidence quality. Evidence is rapidly evolving and previous analysis found that one in five clinical practice recommendations were out of date within three years.2 Fortunately, Australia has pioneered living guideline methods, which use frequent (1–3 monthly) surveillance systems and rapid response pathways using robust Grading of Recommendations Assessment, Development and Evaluation (GRADE) methods to ensure recommendations are up to date.3 This new model is clearly feasible and has demonstrated an increase in trust, frequency of access and intention to apply advice by stakeholders, in areas as diverse as coronavirus disease 2019 and stroke.4, 5 Our experience, contrasting to Starr's, is that this approach is feasible and helpful to develop living guidelines that use reliable GRADE methods and meet National Health and Medical Research Council standards. Living methods (using GRADE) are now considered the gold standard by leading guideline developers such as the National Institute for Health and Care Excellence in England and the World Health Organization. Unfortunately, in Australia there is no national agency to prioritise what guidelines should be developed, let alone sustainable funding to ensure they are kept up to date. We agree with Starr that this must urgently change and call on all governments to invest in CPG infrastructure and capacity. In an age of widespread misinformation and disinformation, it is crucial that Australian clinicians, patients and policy makers have access to reliable, up-to-date, evidence-based information to enable the best possible health care decisions.

All authors are members of the Australian Living Evidence Collaboration Strategic Advisory Committee.

致编辑:儿科临床实践指南(CPGs)1 的合作努力令人鼓舞。1 CPG 为临床医生、健康管理者和政策制定者提供了重要工具。我们非常同意,显然需要在全国范围内协调开展证据综合工作,如有需要,可对其进行调整。Starr1 还就 CPGs 的不理想遵守情况提出了重要观点,包括缺乏时效性和对证据质量的担忧。2 幸运的是,澳大利亚率先采用了 "活指南 "方法,利用频繁(1-3 个月)的监测系统和快速反应途径,采用可靠的 "建议评估、发展和评价分级"(GRADE)方法,确保建议的时效性。这种新模式显然是可行的,并已证明在 2019 年冠状病毒疾病和中风等不同领域,利益相关者的信任度、获取频率和应用建议的意愿都有所提高。目前,英国国家健康与护理卓越研究所(National Institute for Health and Care Excellence)和世界卫生组织(World Health Organization)等领先的指南制定者都将活用方法(使用 GRADE)视为黄金标准。遗憾的是,澳大利亚没有一个国家机构来确定制定指南的优先次序,更不用说提供可持续的资金来确保指南的及时更新。我们同意斯塔尔的观点,认为必须立即改变这种状况,并呼吁各国政府投资于 CPG 基础设施和能力建设。在错误信息和虚假信息泛滥的时代,澳大利亚的临床医生、患者和政策制定者必须能够获得可靠的、最新的、以证据为基础的信息,从而做出最佳的医疗决策。
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引用次数: 0
Physical activity interventions to prevent and manage type 2 diabetes in Aboriginal and Torres Strait Islander people: a systematic review 预防和控制土著居民和托雷斯海峡岛民 2 型糖尿病的体育锻炼干预措施:系统综述。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-21 DOI: 10.5694/mja2.52483
Raymond J Kelly, Rona Macniven, Leonid Churilov, Margaret J Morris, David O'Neal, Elif I Ekinci
<div> <section> <h3> Objectives</h3> <p>To review evidence regarding the impact of physical activity interventions for preventing and managing type 2 diabetes in Aboriginal and Torres Strait Islander Australians.</p> </section> <section> <h3> Study design</h3> <p>We searched for published reports of physical activity interventions for preventing and managing type 2 diabetes in Indigenous adults (18 years or older). There were no exclusion criteria regarding study type or duration, frequency, length, or intensity of physical activity, except that short term interventions were excluded. We assessed the quality of each study using the Joanna Briggs Institute (JBI) critical appraisal tools and the ethical and methodological quality of studies from an Indigenous Australian perspective with the Centre of Research Excellence in Aboriginal Chronic Disease Knowledge Translation and Exchange (CREATE) Critical Appraisal Tool.</p> </section> <section> <h3> Data sources</h3> <p>MEDLINE; Scopus, Embase (Elsevier); Cumulative Index to Nursing and Allied Health Literature (CINAHL), Sports Discus, PsycINFO (EBSCO); Informit Complete; ProQuest Dissertations and Theses, and ProQuest Health and Medicine; each from their inception to 30 October 2022.</p> </section> <section> <h3> Results</h3> <p>The database searches identified 703 potentially relevant records; after removing duplicates and initial screening, the full text of 27 articles was assessed for eligibility. Nine studies met our inclusion criteria: two randomised controlled trials, five cohort studies, one quasi-experimental study, and one repeated cross-sectional study. Eight studies were rated as being of low or medium quality (median JBI score, 54%; interquartile range [IQR], 36–64%); seven studies were rated as being of low to medium ethical and methodological quality from the Indigenous perspective (median CREATE score, 50%; IQR, 36–64%). Six studies reported changes in glycated haemoglobin (HbA<sub>1c</sub>) levels, of which two (both cohort studies) reported significantly lower mean HbA<sub>1c</sub> levels after the intervention, but only one publication provided detailed results. No randomised controlled trials that investigated the effect of a combination of physical activity and dietary change for Indigenous Australians diagnosed with type 2 diabetes were identified. Differences in study design, outcome variables, and the small number of studies precluded meta-analysis.</p> </section> <section> <h3> Conclusions</h3>
研究目的研究设计:研究设计:我们搜索了已发表的关于预防和控制土著成年人(18 岁或以上)2 型糖尿病的体育锻炼干预措施的报告。除了排除短期干预外,没有关于研究类型或持续时间、频率、长度或体育锻炼强度的排除标准。我们使用乔安娜-布里格斯研究所(JBI)的关键评估工具评估了每项研究的质量,并使用原住民慢性病知识转化与交流卓越研究中心(CREATE)的关键评估工具从澳大利亚原住民的角度评估了研究的伦理和方法质量:数据来源:MEDLINE、Scopus、Embase(Elsevier)、Cumulative Index to Nursing and Allied Health Literature(CINAHL)、Sports Discus、PsycINFO(EBSCO)、Informit Complete、ProQuest Dissertations and Theses 和 ProQuest Health and Medicine(ProQuest 健康与医学);每个数据库的检索时间均从开始到 2022 年 10 月 30 日:数据库搜索共发现 703 条潜在相关记录;在去除重复内容并进行初步筛选后,对 27 篇文章的全文进行了资格评估。九项研究符合我们的纳入标准:两项随机对照试验、五项队列研究、一项准实验研究和一项重复横断面研究。八项研究被评为低或中等质量(JBI 评分中位数为 54%;四分位数间距 [IQR],36-64%);七项研究被评为中低道德和方法学质量(CREATE 评分中位数为 50%;四分位数间距 [IQR],36-64%)。六项研究报告了糖化血红蛋白(HbA1c)水平的变化,其中两项(均为队列研究)报告称,干预后平均 HbA1c 水平显著降低,但只有一份出版物提供了详细结果。没有发现任何随机对照试验调查了体育锻炼与饮食改变相结合对确诊为2型糖尿病的澳大利亚土著居民的影响。研究设计、结果变量方面的差异以及研究数量较少排除了进行荟萃分析的可能性:结论:有关体育锻炼干预措施对土著居民 2 型糖尿病影响的高质量研究很少。为了改进研究成果的转化,需要让土著社区成员参与到研究过程的各个层面:PROSPERO CRD42021247496(前瞻性)。
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引用次数: 0
An Aboriginal and Torres Strait Islander adolescent model of primary health care 土著居民和托雷斯海峡岛民青少年初级保健模式。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-21 DOI: 10.5694/mja2.52484
Stephen Harfield, Peter Azzopardi, Gita D Mishra, James S Ward
<p>Aboriginal and Torres Strait Islander adolescents aged 10–24 years represent 30% of the Aboriginal and Torres Strait Islander population.<span><sup>1</sup></span> As a population group, these adolescents are a strong and resilient cohort. However, the health and wellbeing of Aboriginal and Torres Strait Islander adolescents needs improvement and is generally poorer compared with non-Indigenous adolescents.<span><sup>2, 3</sup></span> It is during this life stage that the gap in morbidity and mortality widens between Aboriginal and Torres Strait Islander adolescents and non-Indigenous adolescents, and when a difference in mortality between genders also occurs.<span><sup>2, 3</sup></span> Injury and mental health-related conditions are the leading cause of the increased burden of disease among Aboriginal and Torres Strait Islander adolescents.<span><sup>2, 4</sup></span> Both injury and mental health-related conditions contribute to higher rates of health system engagement, hospitalisations, mortality and the increased health gap between Aboriginal and Torres Strait Islander adolescents and non-Indigenous adolescents.<span><sup>2, 4</sup></span> Similarly, pregnancy-related needs among Aboriginal and Torres Strait Islander adolescent females increase health system engagement, which requires different health system functions. Sexually transmitted infections contribute to health system engagement and excess disease burden experienced by Aboriginal and Torres Strait Islander adolescents. Additionally, as does their engagement in health risk behaviours, such as smoking, alcohol and other drug consumption, and poor diet.<span><sup>2, 3</sup></span></p><p>Eighty per cent of excess mortality among Aboriginal and Torres Strait Islander adolescents is preventable within the current health system.<span><sup>3</sup></span> These deaths are “preventable or treatable within the current health system given timely and effective health care”.<span><sup>3</sup></span> This suggests that within the current health care system, there are many opportunities to intervene and for health gain, and to optimise future health and intergenerational health.</p><p>Aboriginal and Torres Strait Islander adolescents access health care services across a range of settings, including community and primary health care, both mainstream and the community-controlled sector, and hospitals and emergency departments. Yet, evidence suggests the health and wellbeing needs of Aboriginal and Torres Strait Islander adolescents are unmet by current health care services.<span><sup>2, 3</sup></span> Aboriginal and Torres Strait Islander adolescents are less likely to access health care than other groups within the Aboriginal and Torres Strait Islander population.<span><sup>5, 6</sup></span> Additionally, Aboriginal and Torres Strait Islander adolescents encounter several barriers when accessing health care services, including a lack of culturally appropriate services, financial barriers, geograp
与原住民和托雷斯海峡岛民共同设计医疗服务的关键原则包括原住民领 导、文化基础方法、尊重、社区受益、包容性伙伴关系以及透明度和评估、8、16、17 初级医疗保健可以成为土著居民和托雷斯海峡岛民青少年不受歧视的地方。18-20 例如,初级医疗保健可以没有歧视和种族主义,成为土著居民和托雷斯海峡岛民青少年文化上安全的地方,让他们茁壮成长。16 国家安全与优质医疗服务标准和世界卫生组织(WHO)青少年优质医疗服务全球标准确定了政府和医疗服务机构可以采取的行动,以消除歧视并提供文化上安全的医疗服务。18, 19 例如,实施承认青少年脆弱性的政策和程序,提供友好、不评判和尊重青少年的服务。建立一支土著居民和托雷斯海峡岛民医疗队伍对于确保土著居民和托雷斯海峡岛民青少年获得文化适宜的医疗服务至关重要。有证据表明,与非土著医护专业人员相比,土著居民和托雷斯海峡岛民医护专业人员提供的医疗保健服务更适合土著居民和托雷斯海峡岛民的文化,也更能满足他们的需求、16 我们必须向土著居民和托雷斯海峡岛民社区控制的部门学习,了解在培养土著居民和托雷斯海峡岛民卫生工作者队伍方面有哪些行之有效的方法。提高卫生保健工作者的能力是为土著居民和托雷斯海峡岛民青少年提供高质量、有效和文化上安全的卫生保健服务的核心、18 能力被定义为 "按照确定的标准执行特定任务所需的知识、技能、态度和价值观"。21 越来越多的医疗保健专业已经纳入了土著居民和托雷斯海峡岛民特有的能力,并将土著居民和托雷斯海峡岛民的健康和福祉纳入了课程。这一点尤为重要,因为大多数卫生保健专业人员都是在以儿科为重点的时代接受培训的,而且当时传染性疾病在儿童时期比今天青少年所经历的非传染性疾病更为常见。世卫组织为初级保健提供者制定了青少年健康与发展核心能力,以帮助各国制定以能力为基础的青少年健康教育计划。心理健康以及性健康和生殖健康是土著居民和托雷斯海峡岛民青少年的重大关切,但可能是难以解决的问题。全国原住民社区控制健康组织和澳大利亚皇家全科医师学院《原住民和托雷斯海峡岛民预防性健康评估全国指南》25 建议对所有 12-24 岁的年轻人进行社会情感健康评估,并对所有 30 岁或以下性活跃的原住民和托雷斯海峡岛民进行衣原体和淋病筛查。尽管有这些指导方针,但只有不到四分之一的健康评估包括性传播感染检测。26 与时间、技能水平、对主题的舒适度以及不确定如何应对有关的挑战可能是执行不力的原因。土著居民和托雷斯海峡岛民青少年应该能够获得任何初级卫生保健服务,并且作为一个年轻人和在文化上感到安全。
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引用次数: 0
Beyond the silver bullet: closing the equity gap for children within a generation 超越银弹:在一代人的时间内缩小儿童公平差距。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-21 DOI: 10.5694/mja2.52493
Sharon R Goldfeld, Elodie O'Connor, Cindy Pham, Sarah Gray, For the Changing Children's Chances Investigator Group
<p>Over the past decade, inequities in children's health, development and wellbeing have not improved despite great efforts globally.<span><sup>1</sup></span> Inequities are unfair and unjust differences caused by preventable social, economic or geographic factors. Inequities generally persist into adulthood, where they carry high costs for individuals and society,<span><sup>2</sup></span> generating substantial costs across health, education and welfare budgets.<span><sup>3</sup></span> This is an extraordinary system failure for any high income country, including Australia.<span><sup>3</sup></span> Addressing inequities would generate substantial savings across budgets and raise the productivity of society at large, delivering on greater human capital.<span><sup>2, 4</sup></span></p><p>For the first time in history, this generation will not live longer than the generation before it, worldwide.<span><sup>5</sup></span> The chronic disease epidemic is driving much of this trend, with impacts being disproportionately felt by those experiencing adversity.<span><sup>6</sup></span> Opportunities for thriving are becoming increasingly socially patterned. Evidence shows that strategic investments in early childhood are imperative for averting the onset of health challenges and mitigating their societal impacts.<span><sup>7</sup></span> Yet Australian children on a persistently disadvantaged trajectory over early childhood have a seven-fold increased risk of having poorer outcomes in multiple developmental domains by late childhood, compared with the most advantaged children.<span><sup>8</sup></span></p><p>Although it might seem an unachievable goal, with the right political will and resource commitments, Australia could close the child equity gap within a generation. Perhaps more than any other time in the past decade, current federal and state agendas align with this aspiration, with the latest intergenerational report underscoring the need for urgency.<span><sup>4</sup></span> Responding to current policy interests can inform priority areas and the intervention levers that could be considered. Some existing Australian policy interests include: Early Years Strategy,<span><sup>9</sup></span> National Framework for Protecting Australia's Children,<span><sup>10</sup></span> Entrenched Disadvantage Package,<span><sup>11</sup></span> National Children's Mental Health and Wellbeing Strategy,<span><sup>12</sup></span> and Early Childhood Education and Care agendas.<span><sup>13</sup></span></p><p>This article suggests a path forward that draws on the critical thinking of multidisciplinary leaders (across economics, health, education, social care, legislation and policy) and converges on key themes of “thinking and doing” that can and should inform the early years policy and research agenda for Australia. These collaborations are essential if Australian governments are prepared to deliver on closing the equity gap with the level of urgency required.</p><p>Rad
17, 20 要真正缩小公平差距,就必须超越传统研究和政策范式中普遍存在的银弹思维,步入复杂性。要解决错综复杂的不公平问题,就需要采取同样复杂的干预方法。17, 20-23 这应该是对研究人员和政策制定者已知有效的干预措施的一个相对直接的选择,以及更好地利用现有的教育、卫生和社会基础设施来有目的地纠正不公平现象(方框 2)。这种方法以适度普遍性原则为基础,既能确保普遍服务基础的好处,又能进行调整, 确保规模和强度与需求水平相称,这也是有效解决不平等问题所必需的:(i) 实现最大影响;(ii) 在整个生命过程中仔细考虑;(iii) 尽可能最大限度地利用现有资源和支出;(iv) 利用数据和指标来推动系统变革;(v) 通过资源充足、灵活的共同设计过程实现快速实施;(vi) 通过生态路径(即从个人到政策变革)进行叠加。以地方和社区为主导的创新项目已经通过综合服务交付项目将这些原则付诸实践,并取得了可喜的成果,例如,这些项目就有很多值得学习的地方:健全的数据系统和高质量的关键指标对于更准确、更有效地识别、解决和监测不公平现象至关重要。在澳大利亚,人们对将不同部门的行政数据联系起来的兴趣越来越大,投资也越来越多。关联的行政数据资产,如澳大利亚政府个人层面综合数据资产(PLIDA)30 、即将推出的生命历程数据倡议31 和国家残疾数据资产32 ,为生成可操作的政策相关证据提供了一个既省时又省钱的机会。然而,关键数据缺口(包括有关家庭环境、儿童结果和一些重点人群的有限数据)以及有关数据准确性、完整性和及时性的局限性,会妨碍我们了解在何处以及如何分配资源以有效解决不平等问题。澳大利亚儿童纵向研究》(Longitudinal Study of Australian Children)自 2004 年 5 月以来一直对 5107 名婴儿的成长情况进行跟踪研究,33 这就是一个具有人口代表性的队列研究的例子,该研究通过大量的数据链接得到了加强。最近的一个例子是维多利亚一代(Generation Victoria,GenV),这是一个前瞻性的全州多用途出生和父母队列,始于 2021 年 10 月34 ;迄今已招募了超过 12 万名婴儿和父母。GenV 代表了维多利亚州,因此在大多数方面也代表了澳大利亚。通过与各州和联邦行政数据的广泛链接,GenV 将获得所需的丰富而广泛的信息,以支持对儿童整个生态系统中与政策相关的叠加干预措施进行评估。重要的是要考虑如何更广泛地共享这些类型的数据,以促进跨部门合作,并让政治和社区领袖、倡导者、研究人员和服务用户参与进来,他们对于叠加方法的概念化和实施至关重要。显然,只要有足够的资源,加上社区和政治意愿,几乎任何事情都可以实现。每年约有 72 000 名澳大利亚婴儿出生在逆境中,35 他们健康长寿、有所作为的机会也随之减少。今天出生的孩子应该比他们的父母拥有更公平的成人结果,而不是更少。研究人员和政策制定者都有一种紧迫感和动力。但同时也有一种使命感。没有相关信息披露。
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引用次数: 0
Young voices, healthy futures: the rationale for lowering the voting age to 16 年轻的声音,健康的未来:将投票年龄降至 16 岁的理由。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-21 DOI: 10.5694/mja2.52496
Kevin Kapeke, Planning Saw, Edward Krutsch, Claudia Burgner, Hannah Pitt, Ravin Desai, Khalid Muse, Jennifer Rowan, Charlize Nalupta, Judith Bessant, Susan M Sawyer, Sara Wardak
<p>The saying “If you don't vote, you don't count” highlights the importance of exercising our democratic right to vote in Australia.<span><sup>1</sup></span> Voting is a fundamental mechanism through which citizens can articulate their concerns and advocate for responsive governance.<span><sup>1</sup></span> Children and young people are currently paying a high price, especially in terms of their health, because individuals aged under 18 years are not allowed to vote. The disenfranchisement of young people perpetuates political disillusionment and exacerbates health disparities.<span><sup>2</sup></span> Historically, marginalised groups have experienced similar patterns of exclusion, leading to systemic neglect of their needs.<span><sup>3</sup></span></p><p>In this 2024 <i>MJA</i> supplement article for the Future Healthy Countdown 2030,<span><sup>4</sup></span> we argue that lowering the voting age to 16 years would empower young people and the political system to address inequities and build an inclusive society that promotes wellbeing. By examining the association between political participation and health outcomes, this article positions voting not merely as a democratic right but as a strategic intervention to improve public health (Box). This argument is grounded in the World Health Organization's conceptualisation of social determinants of health, which acknowledges that participation in political processes is essential for individual and community wellbeing.<span><sup>5</sup></span></p><p>Political participation is a critical social determinant of health, fostering social inclusion, empowerment and equity, which are essential for mental and physical wellbeing.<span><sup>6</sup></span> Voting, as a direct form of political participation, empowers individuals with a sense of agency over decisions that affect their lives.<span><sup>3</sup></span></p><p>Historically, expanding voting rights has led to improved health outcomes. In the United States, for example, the enfranchisement of women and racial minorities reduced inequities, resulting in significant public health gains, including better education and income, and increased longevity.<span><sup>7, 8</sup></span> These precedents suggest that extending voting rights to young people could similarly drive positive health outcomes by ensuring their representation in policy making.</p><p>Young people face barriers to equitable access to health services, such as primary health care, and issues of trust and confidentiality, compounded by complex health issues such as sexual health, mental health, family violence and homelessness.<span><sup>9</sup></span> Since the coronavirus disease 2019 (COVID-19) pandemic, young people have been disproportionately affected by challenges such as the cost-of-living crisis, high education costs, lack of affordable housing, generational wealth inequities, and a highly casualised youth workforce.<span><sup>10</sup></span></p><p>Currently, major social and policy
例如,为支持首次投票的选民并确保平稳过渡,应采取有力的公民教育计划、关于投票责任的明确沟通以及针对年轻选民的提醒和宣传活动等支持性措施。此外,在早期阶段对不参加投票者给予宽限或宽限期,有助于减轻对刑事犯罪的恐惧,培养积极的投票习惯。将投票年龄降至 16 岁将承认年轻人有权利和能力积极参与塑造他们现在和未来的生活。这种改变将鼓励政治家考虑年轻人的关切,促进公民参与,并加强澳大利亚选举制度的民主传统。历史和国际范例都表明,扩大投票权能够改善健康状况和社会效益。53 虽然将投票权扩展至年轻公民并不能完全解决政治幻灭问题,但这是弥合代际鸿沟、促进以预防和主动为导向的健康政策的重要一步。40 因此,关键问题不是为什么要赋予年轻人投票权,而是为什么要剥夺他们的投票权。
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引用次数: 0
Environmental footprinting in health care: a primer 医疗保健中的环境足迹:入门指南。
IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-10-17 DOI: 10.5694/mja2.52481
Jacob Fry, Angie Bone, Keiichiro Kanemoto, Carolynn L Smith, Nick Watts
<p>Health care systems are responsible for 4–5% of global greenhouse gas (GHG) emissions.<span><sup>1, 2</sup></span> There is increasing pressure to reduce the environmental effects of health care as more health professionals recognise its contribution to climate change.<span><sup>3, 4</sup></span> However, measuring environmental effects and assessing progress towards decarbonisation are not trivial processes because the mechanisms driving environmental burdens are often hidden. Although much of the early focus in health has been on decarbonisation of building and transport assets, most of health care's GHG emissions occur within the supply chains that provision the health care system before the final delivery of services.<span><sup>5</sup></span></p><p>This article is intended to serve as a beginner's introduction to the environmental footprinting techniques that can be applied to uncover health care's environmental impacts, including impacts occurring along supply chains. This article focuses on GHG emissions, but many other pollutants and environmental stressors can be assessed using these methods.</p><p>Environmental impacts can be separated into “direct” and “indirect” impacts. Direct impacts occur within an organisation's physical boundary, for example hospital grounds. Indirect impacts occur outside this immediate boundary, for example impacts from purchased products. Direct impacts are relatively easy to estimate using fossil fuel consumption and utility bills. In contrast, estimating indirect emissions is more challenging for health care organisations and requires detailed data on the quantity or cost of procured products and services and the application of environmental footprinting techniques. An organisation's indirect emissions form part of their suppliers’ direct emissions and likely occur in other regions and jurisdictions, rendering them more abstract and intangible.</p><p>Quantifying indirect environmental impacts requires consideration of the supply chains delivering goods and services to final consumption. Supply chains link production layers together, where at each stage numerous inputs and components are combined to make intermediate products. This can be depicted as a tree branching upwards and outwards from the consumer, with each node representing a production stage (Box 1). Here, “upstream” refers to layers occurring before the product reaches a consumer, and “downstream” refers to layers after final consumption, including disposal of the product.</p><p>Environmental effects can occur at each layer and accumulate along the supply chain as more layers are included.<span><sup>6</sup></span> Eventually, supply chains reach consumers as final products. Accounting for all upstream environmental impacts associated with a product or service is onerous because of the large number of production layers and the many inputs into each layer. An illustrative example of supply chain is “fossil fuel combustion > petrochemical refini
1, 2 随着越来越多的医疗专业人士认识到医疗服务对气候变化的影响,减少医疗服务对环境影响的压力与日俱增。3, 4 然而,衡量环境影响和评估去碳化进展并非易事,因为造成环境负担的机制往往是隐性的。尽管医疗卫生领域的早期关注点主要集中在建筑和运输资产的去碳化上,但医疗卫生系统的大部分温室气体排放都发生在最终提供服务之前的供应链上。本文的重点是温室气体排放,但许多其他污染物和环境压力源也可以使用这些方法进行评估。环境影响可分为 "直接 "影响和 "间接 "影响。环境影响可分为 "直接 "影响和 "间接 "影响。直接影响发生在组织的物理边界内,例如医院场地。间接影响发生在这一直接边界之外,例如外购产品造成的影响。利用化石燃料消耗和公用事业账单估算直接影响相对容易。相比之下,间接排放的估算对医疗机构来说更具挑战性,它需要有关采购产品和服务的数量或成本的详细数据,以及环境足迹技术的应用。一个组织的间接排放是其供应商直接排放的一部分,很可能发生在其他地区和司法管辖区,因此更加抽象和无形。量化间接环境影响需要考虑将产品和服务运送到最终消费的供应链。供应链将各生产层连接在一起,在每个阶段都有许多投入和组件组合成中间产品。这可以描绘成一棵从消费者向上向外延伸的树,每个节点代表一个生产阶段(方框 1)。在这里,"上游 "指的是产品到达消费者之前的层级,"下游 "指的是最终消费之后的层级,包括产品的处置。环境影响可能发生在每一层级,并随着层级的增加沿着供应链累积。6 最终,供应链会以最终产品的形式到达消费者手中。由于产品或服务的生产层级较多,且每一层都有许多投入,因此对与产品或服务相关的所有上游环境影响进行核算是一项繁重的工作。化石燃料燃烧&gt; 石油化工精炼&gt; 塑料样本罐&gt; 病理服务 "就是供应链的一个示例,它只是促成 "病理服务 "的众多供应链之一。当所有重要活动都不在边界内时,该边界被认为是 "不完整的",导致部分环境影响未被计算9。在计算产品或流程的全部环境足迹以及进行比较时,对已定义的系统边界的认识非常重要。9 在计算产品或工艺的全部环境足迹以及进行比较时,认识所定义的系统边界非常重要。未计影响的严重程度取决于工艺和活动,例如,可能包括基本建设工程、基础设施和服务部门产生的影响。方框 2 描述了与最终消费和中间生产阶段相关的 系统边界。尽管这些范围已被普遍使用,但它们只是 一种简化,并不总是与组织结构或功能完全一致。例如,门诊病人运输产生的排放可归入医疗系统的范围 1 排放;但病人自行运输产生的排放仍未计算在内。此外,范围框架没有考虑供应链中上游和下游参与者之间的共同排放责任。这些困难反映了在减排责任归属方面更广泛的社会复杂性。11 可区分两种主要的环境足迹方法:生命周期评估 (LCA) 和环境扩展投入产出分析 (EE-IOA)。一般来说,涉及诊断方法和治疗的问题最好使用生命周期评估技术,而评估卫生系统层面的总体进展则更适合 EE-IOA 技术。国际标准化组织 (ISO) 14040:2006 和 14044:2006 为进行生命周期评估的从业人员提供了指南。 欧盟正在引入新的法规来打击 "洗绿 "行为26 ,并对如何进行生命周期评估制定了自己的指导方针27 。然而,在许多卫生系统中,环境数据的收集、存储和分析系统往往是有限的,而且通常没有标准化,也没有与临床和人口结果联系起来。我们并不是说环境足迹是医护人员的主要职责,也不是说对环境影响的考虑应优先于临床结果。相反,环境的可持续发展应被视为质量、安全和良好管理的一个方面,与患者和人口的健康结果并列。
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引用次数: 0
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Medical Journal of Australia
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