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The next 1000 days: the forgotten ages of child health 未来 1000 天:被遗忘的儿童健康时代
Pub Date : 2024-11-21 DOI: 10.1016/s0140-6736(24)02553-4
No Abstract
无摘要
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引用次数: 0
Expanding therapeutic options in Crohn's disease 扩展克罗恩病的治疗方案
Pub Date : 2024-11-21 DOI: 10.1016/s0140-6736(24)01937-8
Thomas P Chapman, Jack Satsangi
No Abstract
无摘要
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引用次数: 0
Halving premature death and improving quality of life at all ages: cross-country analyses of past trends and future directions 将所有年龄段的过早死亡人数减半并提高生活质量:对过去趋势和未来方向的跨国分析
Pub Date : 2024-11-21 DOI: 10.1016/s0140-6736(24)02417-6
Ole F Norheim, Angela Y Chang, Sarah Bolongaita, Mariana Barraza-Lloréns, Ayodamope Fawole, Lia Tadesse Gebremedhin, Eduardo González-Pier, Prabhat Jha, Emily K Johnson, Omar Karlsson, Mizan Kiros, Sarah Lewington, Wenhui Mao, Osondu Ogbuoji, Muhammad Pate, Jennifer L Sargent, Xuyang Tang, David Watkins, Gavin Yamey, Dean T Jamison, Richard Peto

Background

Although death in old age is unavoidable, premature death—defined here as death before age 70 years—is not. To assess whether halving premature mortality by 2050 is feasible, we examined the large variation in premature death rates before age 70 years and trends over the past 50 years (1970–2019), covering ten world regions and the 30 most-populous nations. This analysis was undertaken in conjunction with the third report of The Lancet Commission on Investing in Health: Global Health 2050: the path to halving premature death by mid-century.

Methods

In this cross-country analysis of past mortality trends and future directions, all analyses on the probability of premature death (PPD) were conducted using life tables from the UN World Population Prospects 2024. For each sex, country, and year, probability of death was calculated from these life tables with 1-year age-specific mortality rates.

Findings

Globally, PPD decreased from 56% in 1970 to 31% in 2019, although some countries saw reversals because of conflict, social instability, or HIV and AIDS. Child mortality has decreased faster than adult mortality. Among all countries, 34 halved their PPD over three decades between 1970 and 2019. Among the 30 most-populous countries, seven countries, with varying levels of baseline PPD and income, halved their PPD in the past half century. Seven of the most-populous countries had average annual rates of improvement in the period 2010–19 that, if sustained, could lead to a halving of PPD by 2050, including Korea (3·9%), Bangladesh (2·8%), Russia (2·7%), Ethiopia (2·4%), Iran (2·4%), South Africa (2·4%), and Türkiye (2·3%).

Interpretation

Halving premature death by 2050 is feasible, although substantial investments in child and adult health are needed to sustain or accelerate the rate of improvement for high-performing and medium-performing countries. Particular attention must be paid to countries with very low or a worsening rate of improvement in PPD. By reducing premature mortality, more people will live longer and more healthy lives. However, as people live longer, the absolute number of years lived with chronic disease will increase and investments in services reducing chronic disease morbidity are needed.

Funding

The Norwegian Agency for Development Cooperation, the Bill & Melinda Gates Foundation, and a Norwegian Research Council Centre of Excellence grant.
背景虽然老年死亡不可避免,但过早死亡(此处定义为 70 岁之前的死亡)却并非如此。为了评估到 2050 年将过早死亡率减半是否可行,我们研究了 70 岁前过早死亡率的巨大差异以及过去 50 年(1970-2019 年)的趋势,涵盖了世界 10 个地区和 30 个人口最多的国家。这项分析是结合柳叶刀健康投资委员会的第三份报告进行的:在这项关于过去死亡率趋势和未来走向的跨国分析中,所有关于过早死亡概率(PPD)的分析都是使用联合国《2024 年世界人口展望》中的生命表进行的。对于每个性别、国家和年份,死亡概率都是根据这些生命表和 1 年特定年龄死亡率计算得出的。研究结果从全球来看,早亡概率从 1970 年的 56% 降至 2019 年的 31%,但一些国家由于冲突、社会不稳定或艾滋病毒和艾滋病的影响,早亡概率出现了逆转。儿童死亡率的下降速度快于成人死亡率。在所有国家中,有34个国家在1970年至2019年的30年间将儿童死亡率降低了一半。在人口最多的 30 个国家中,有 7 个国家在过去半个世纪中将 PPD 减少了一半,这些国家的 PPD 基线和收入水平各不相同。在人口最多的国家中,有 7 个国家在 2010-19 年期间的年均改善率如果保持不变,到 2050 年可将 PPD 减少一半,这些国家包括韩国(3-9%)、孟加拉国(2-8%)、俄罗斯(2-7%)、埃塞俄比亚(2-4%)、伊朗(2-4%)、南非(2-4%)和土耳其(2-3%)。解释到 2050 年减少过早死亡是可行的,尽管需要对儿童和成人健康进行大量投资,以保持或加快高绩效和中等绩效国家的改善速度。必须特别关注 PPD 改善率非常低或正在恶化的国家。通过降低过早死亡率,更多的人将活得更长、更健康。挪威发展合作署、比尔-盖茨基金会和挪威研究理事会卓越中心的资助。
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引用次数: 0
Declaration of Helsinki's missed opportunity for healthy volunteer trials 赫尔辛基宣言》让健康志愿者试验错失良机
Pub Date : 2024-11-21 DOI: 10.1016/s0140-6736(24)02431-0
François Bompart, Jill A Fisher, Sucheta Banerjee Kurundkar, François Hirsch, Shadreck Mwale
No Abstract
无摘要
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引用次数: 0
Skin biopsy findings of dyskeratotic keratinocytes and vacuolar interface change in a patient with Still's disease 一名斯蒂尔病患者皮肤活检发现角化不良的角质细胞和空泡界面变化
Pub Date : 2024-11-21 DOI: 10.1016/s0140-6736(24)02419-x
Derrick H Y Chong, Sylvia Pasternak, Trudy Taylor, Sam Armstrong, Kerri Purdy, Luke Y C Chen

Section snippets

Contributors

We were all involved in providing care for the patient. We were all involved in writing and editing the manuscript. Written consent for publication was obtained from the patient.

Declaration of interests

We declare no competing interests.

Acknowledgments

LYCC's work is supported by the Hsu & Taylor Family through the UBC & VGH Foundation.
章节片段贡献者我们都参与了对患者的护理。我们都参与了手稿的撰写和编辑。利益声明我们声明不存在任何利益冲突。致谢LYCC的工作得到了Hsu & Taylor家族通过UBC & VGH基金会提供的支持。
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引用次数: 0
UNRWA's work is at risk again 近东救济工程处的工作再次面临风险
Pub Date : 2024-11-20 DOI: 10.1016/s0140-6736(24)02476-0
Bassam Abu Hamad, Zeina Jamaluddine, Sarah Aly, Mohammad Salayma, Yara Asi, Hani Mowafi, Francesco Checchi, Miho Sato, Asli Bali, Paul Spiegel
No Abstract
无摘要
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引用次数: 0
Temporary blood flow arrest during endovascular thrombectomy for acute ischaemic stroke 急性缺血性脑卒中血管内血栓切除术中的暂时性血流停止
Pub Date : 2024-11-20 DOI: 10.1016/s0140-6736(24)02461-9
Permesh Singh Dhillon, Thanh N Nguyen
No Abstract
无摘要
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引用次数: 0
Balloon guide catheters for endovascular thrombectomy in patients with acute ischaemic stroke due to large-vessel occlusion in China (PROTECT-MT): a multicentre, open-label, blinded-endpoint, randomised controlled trial 中国大血管闭塞所致急性缺血性卒中患者使用球囊导引导管进行血管内血栓切除术(PROTECT-MT):一项多中心、开放标签、盲终点、随机对照试验
Pub Date : 2024-11-20 DOI: 10.1016/s0140-6736(24)02315-8
Jianmin Liu, Yu Zhou, Lei Zhang, Zifu Li, Wenhuo Chen, Yueqi Zhu, Xiaoxi Yao, Liyong Zhang, Shen Liu, Ya Peng, Ming Wei, Quanbin Zhang, Hansheng Shu, Shouchun Wang, Wenhua Liu, Shu Wan, Tong Li, Yibin Fang, Hongxing Han, Guang Zhang, T Yu
<h3>Background</h3>The effectiveness of using a balloon guide catheter during endovascular thrombectomy in patients with acute ischaemic stroke due to large vessel occlusion of the anterior circulation remains uncertain. We aimed to assess the effectiveness and safety of using a balloon guide catheter during endovascular thrombectomy, compared with using a conventional guide catheter, in this patient population.<h3>Methods</h3>We conducted a multicentre, open-label, blinded-endpoint, randomised controlled trial at 28 hospitals in China. Adults aged 18 years or older with acute ischaemic stroke who were able to receive endovascular thrombectomy within 24 h after symptom onset, according to local guidelines, were eligible. Patients were randomly assigned (1:1) to the balloon guide catheter group or the conventional guide catheter group using a central internet-based system with a minimisation algorithm. The treating physicians and patients were aware of treatment allocation, but clinical outcomes were collected by local trained physicians who were masked. Neurological assessments were performed at baseline, 24 h after randomisation, and at 7 days or hospital discharge (whichever occurred first). The primary outcome was functional recovery, assessed by change in modified Rankin Scale (mRS) scores (ranging from 0 [no symptoms] to 6 [death]) at 90 days in the intention-to-treat population and obtained from structured interviews. Treatment effect was estimated using ordinal logistic regression with adjustment for site and baseline prognostic factors (time from symptom onset to randomisation, the preferred thrombectomy strategy, baseline National Institutes of Health Stroke Scale score, prestroke function [estimated mRS score], and age). This trial is registered with <span><span>ClinicalTrials.gov</span><svg aria-label="Opens in new window" focusable="false" height="20" viewbox="0 0 8 8"><path d="M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z"></path></svg></span>, <span><span>NCT05592054</span><svg aria-label="Opens in new window" focusable="false" height="20" viewbox="0 0 8 8"><path d="M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z"></path></svg></span> (terminated).<h3>Findings</h3>Between Feb 7 and Nov 13, 2023, 1698 patients were assessed for eligibility and 329 were randomly assigned to the balloon guide catheter group (n=164) or conventional guide catheter group (n=165) when the trial was paused and subsequently terminated on April 18, 2024, due to safety concerns. The median age was 69 years (IQR 59–76). Of 329 patients, 201 (61%) were male and 128 (39%) were female. Participants in the balloon guide catheter group had significantly worse scores on the mRS at 90 days than those in the conventional guide catheter group (adjusted common odds ratio 0·66 [95% CI 0·45–0·98]; p=0·037). All-cause mortality at 90 days was numerically higher in the balloon guide catheter
背景在前循环大血管闭塞引起的急性缺血性卒中患者的血管内血栓切除术中使用球囊导引导管的有效性仍不确定。我们的目的是评估在血管内血栓切除术中使用球囊导引导管与使用传统导引导管相比,在这一患者群体中的有效性和安全性。符合条件的急性缺血性脑卒中患者年龄在 18 岁或以上,根据当地指南可在症状出现后 24 小时内接受血管内血栓切除术。通过基于互联网的中央系统和最小化算法将患者随机分配(1:1)到球囊导引导管组或传统导引导管组。主治医生和患者均知晓治疗分配情况,但临床结果由当地经过培训的医生收集,这些医生均被蒙蔽。分别在基线、随机分配后 24 小时、7 天或出院时(以先发生者为准)进行神经评估。主要结果是功能恢复情况,通过结构化访谈获得的改良Rankin量表(mRS)评分(从0分(无症状)到6分(死亡))的变化来评估意向治疗人群90天后的功能恢复情况。采用序数逻辑回归法估算治疗效果,并对治疗部位和基线预后因素(从症状出现到随机化的时间、首选血栓切除策略、美国国立卫生研究院卒中量表基线评分、卒中前功能[估计mRS评分]和年龄)进行调整。研究结果2023年2月7日至11月13日,1698名患者接受了资格评估,329名患者被随机分配到球囊导引导管组(164人)或传统导引导管组(165人),由于安全性问题,试验暂停,随后于2024年4月18日终止。中位年龄为 69 岁(IQR 59-76)。在 329 名患者中,201 人(61%)为男性,128 人(39%)为女性。球囊导引导管组患者 90 天后的 mRS 评分明显低于传统导引导管组患者(调整后常见几率比 0-66 [95% CI 0-45-0-98];P=0-037)。球囊导引导管组 90 天后的全因死亡率高于常规导引导管组(39 [24%] vs 26 [16%])。在颅内出血、无症状性颅内出血或其他严重不良事件方面,组间差异无统计学意义。基金资助国家自然科学基金委、上海市医院发展中心、上海生物医药产业促进中心、通桥医疗科技有限公司。翻译摘要的中文翻译请参见补充材料部分。
{"title":"Balloon guide catheters for endovascular thrombectomy in patients with acute ischaemic stroke due to large-vessel occlusion in China (PROTECT-MT): a multicentre, open-label, blinded-endpoint, randomised controlled trial","authors":"Jianmin Liu, Yu Zhou, Lei Zhang, Zifu Li, Wenhuo Chen, Yueqi Zhu, Xiaoxi Yao, Liyong Zhang, Shen Liu, Ya Peng, Ming Wei, Quanbin Zhang, Hansheng Shu, Shouchun Wang, Wenhua Liu, Shu Wan, Tong Li, Yibin Fang, Hongxing Han, Guang Zhang, T Yu","doi":"10.1016/s0140-6736(24)02315-8","DOIUrl":"https://doi.org/10.1016/s0140-6736(24)02315-8","url":null,"abstract":"&lt;h3&gt;Background&lt;/h3&gt;The effectiveness of using a balloon guide catheter during endovascular thrombectomy in patients with acute ischaemic stroke due to large vessel occlusion of the anterior circulation remains uncertain. We aimed to assess the effectiveness and safety of using a balloon guide catheter during endovascular thrombectomy, compared with using a conventional guide catheter, in this patient population.&lt;h3&gt;Methods&lt;/h3&gt;We conducted a multicentre, open-label, blinded-endpoint, randomised controlled trial at 28 hospitals in China. Adults aged 18 years or older with acute ischaemic stroke who were able to receive endovascular thrombectomy within 24 h after symptom onset, according to local guidelines, were eligible. Patients were randomly assigned (1:1) to the balloon guide catheter group or the conventional guide catheter group using a central internet-based system with a minimisation algorithm. The treating physicians and patients were aware of treatment allocation, but clinical outcomes were collected by local trained physicians who were masked. Neurological assessments were performed at baseline, 24 h after randomisation, and at 7 days or hospital discharge (whichever occurred first). The primary outcome was functional recovery, assessed by change in modified Rankin Scale (mRS) scores (ranging from 0 [no symptoms] to 6 [death]) at 90 days in the intention-to-treat population and obtained from structured interviews. Treatment effect was estimated using ordinal logistic regression with adjustment for site and baseline prognostic factors (time from symptom onset to randomisation, the preferred thrombectomy strategy, baseline National Institutes of Health Stroke Scale score, prestroke function [estimated mRS score], and age). This trial is registered with &lt;span&gt;&lt;span&gt;ClinicalTrials.gov&lt;/span&gt;&lt;svg aria-label=\"Opens in new window\" focusable=\"false\" height=\"20\" viewbox=\"0 0 8 8\"&gt;&lt;path d=\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\"&gt;&lt;/path&gt;&lt;/svg&gt;&lt;/span&gt;, &lt;span&gt;&lt;span&gt;NCT05592054&lt;/span&gt;&lt;svg aria-label=\"Opens in new window\" focusable=\"false\" height=\"20\" viewbox=\"0 0 8 8\"&gt;&lt;path d=\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\"&gt;&lt;/path&gt;&lt;/svg&gt;&lt;/span&gt; (terminated).&lt;h3&gt;Findings&lt;/h3&gt;Between Feb 7 and Nov 13, 2023, 1698 patients were assessed for eligibility and 329 were randomly assigned to the balloon guide catheter group (n=164) or conventional guide catheter group (n=165) when the trial was paused and subsequently terminated on April 18, 2024, due to safety concerns. The median age was 69 years (IQR 59–76). Of 329 patients, 201 (61%) were male and 128 (39%) were female. Participants in the balloon guide catheter group had significantly worse scores on the mRS at 90 days than those in the conventional guide catheter group (adjusted common odds ratio 0·66 [95% CI 0·45–0·98]; p=0·037). All-cause mortality at 90 days was numerically higher in the balloon guide catheter ","PeriodicalId":22898,"journal":{"name":"The Lancet","volume":"191 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142678260","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Drugs for dyslipidaemia: the legacy effect of the Scandinavian Simvastatin Survival Study (4S) 治疗血脂异常的药物:斯堪的纳维亚辛伐他汀生存研究(4S)的遗产效应
Pub Date : 2024-11-19 DOI: 10.1016/s0140-6736(24)02089-0
Timo E Strandberg, Petri T Kovanen, Donald M Lloyd-Jones, Frederick J Raal, Raul D Santos, Gerald F Watts
Since the discovery of statins and the Scandinavian Simvastatin Survival Study (4S) results three decades ago, remarkable advances have been made in the treatment of dyslipidaemia, a major risk factor for atherosclerotic cardiovascular disease. Safe and effective statins remain the cornerstone of therapeutic approach for this indication, including for children with genetic dyslipidaemia, and are one of the most widely prescribed drugs in the world. However, despite the affordability of generic statins, they remain underutilised worldwide. The use of ezetimibe to further decrease plasma LDL cholesterol and the targeting of other atherogenic lipoproteins, such as triglyceride-rich lipoproteins and lipoprotein(a), are likely to be required to further reduce atherosclerotic cardiovascular disease events. Drugs directed at these lipoproteins, including gene silencing and editing methods that durably suppress the production of proteins, such as PCSK9 and ANGPTL3, open novel therapeutic options to further reduce the development of atherosclerotic cardiovascular disease.
自从三十年前发现他汀类药物和斯堪的纳维亚辛伐他汀生存研究(4S)结果以来,血脂异常(动脉粥样硬化性心血管疾病的主要危险因素)的治疗取得了显著进展。安全有效的他汀类药物仍然是这一适应症(包括遗传性血脂异常儿童)治疗方法的基石,也是世界上处方量最大的药物之一。然而,尽管非专利他汀类药物价格低廉,但在全球范围内仍未得到充分利用。要进一步减少动脉粥样硬化性心血管疾病的发生,可能需要使用依折麦布来进一步降低血浆低密度脂蛋白胆固醇,并针对其他致动脉粥样硬化脂蛋白,如富含甘油三酯的脂蛋白和脂蛋白(a)。针对这些脂蛋白的药物,包括持久抑制 PCSK9 和 ANGPTL3 等蛋白生成的基因沉默和编辑方法,为进一步减少动脉粥样硬化性心血管疾病的发生提供了新的治疗选择。
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引用次数: 0
The next 1000 days: building on early investments for the health and development of young children 未来 1000 天:在早期投资的基础上促进幼儿的健康和发展
Pub Date : 2024-11-18 DOI: 10.1016/s0140-6736(24)01389-8
Catherine E Draper, Aisha K Yousafzai, Dana C McCoy, Jorge Cuartas, Jelena Obradović, Sunil Bhopal, Jane Fisher, Joshua Jeong, Sonja Klingberg, Kate Milner, Lauren Pisani, Aditi Roy, Jonathan Seiden, Christopher R Sudfeld, Stephanie V Wrottesley, Günther Fink, Milagros Nores, Mark S Tremblay, Anthony D Okely
Following the first 1000 days of life that span from conception to two years of age, the next 1000 days of a child's life from 2–5 years of age offer a window of opportunity to promote nurturing and caring environments, establish healthy behaviours, and build on early gains to sustain or improve trajectories of healthy development. This Series paper, the first of a two-paper Series on early childhood development and the next 1000 days, focuses on the transition to the next 1000 days of the life course, describes why this developmental period matters, identifies the environments of care, risks, and protective factors that shape children's development, estimates the number of children who receive adequate nurturing care, and examines whether current interventions are meeting children's needs. Paper 2 focuses on the cost of inaction and the implications of not investing in the next 1000 days. In low-income and middle-income countries (LMICs), only 62 million children aged 3 and 4 years (25·4%) currently receive adequate nurturing care during the next 1000 days, leaving 181·9 million children exposed to risks that jeopardise their healthy development. Inputs across nurturing care dimensions of health, nutrition, protection, responsive care, and learning vary substantially across countries. In LMICs, although 86·2% of children have a healthy weight in this period, less than one in three children have access to developmental stimulation or are protected from physical punishment, and only 38·8% have access to early childhood care and education services. Intervention research in LMICs in the next 1000 days is scarce. The continuity of developmentally appropriate nurturing care, coordination across health, education, and protection sectors, and the implementation of interventions to support caregivers and improve the quality of education and care remain top priorities in this period. These sectors play key roles in promoting quality early care and education for this age group, which will help maximise developmental potential and opportunities of children globally and help progress towards the achievement of the Sustainable Development Goals.
在从受孕到两岁的生命最初 1000 天之后,2-5 岁儿童生命中的下一个 1000 天为我们提供了一个机会之窗,以促进养育和关爱环境,建立健康行为,并在早期收获的基础上保持或改善健康发展的轨迹。本系列论文是 "儿童早期发展与未来 1000 天 "系列两篇论文中的第一篇,重点关注生命历程中向未来 1000 天的过渡,阐述这一发展时期的重要性,确定影响儿童发展的照料环境、风险和保护因素,估算获得充分养育照料的儿童人数,并研究当前的干预措施是否满足儿童的需求。论文 2 的重点是不作为的代价以及不对未来 1000 天进行投资的影响。在低收入和中等收入国家(LMICs),目前只有 6200 万 3-4 岁儿童(25-4%)在未来 1000 天内得到了充分的养育关怀,这使得 1.81 亿-900 万儿童面临危及其健康成长的风险。各国在健康、营养、保护、有针对性的照料和学习等养育照料方面的投入差别很大。在低收入和中等收入国家,虽然有 86-2% 的儿童在这一时期体重健康,但只有不到三分之一的儿童能够获得发育刺激或免受体罚,只有 38-8% 的儿童能够获得幼儿保育和教育服务。在低收入和中等收入国家,对未来 1000 天的干预研究很少。在这一时期,持续提供适合儿童发展的培养性保育,协调卫生、教育和保护部门,以及实施干预措施以支持保育人员并提高教育和保育质量,仍是当务之急。这些部门在促进这一年龄组的优质早期保育和教育方面发挥着关键作用,这将有助于最大限度地发挥全球儿童的发展潜力和机会,并有助于在实现可持续发展目标方面取得进展。
{"title":"The next 1000 days: building on early investments for the health and development of young children","authors":"Catherine E Draper, Aisha K Yousafzai, Dana C McCoy, Jorge Cuartas, Jelena Obradović, Sunil Bhopal, Jane Fisher, Joshua Jeong, Sonja Klingberg, Kate Milner, Lauren Pisani, Aditi Roy, Jonathan Seiden, Christopher R Sudfeld, Stephanie V Wrottesley, Günther Fink, Milagros Nores, Mark S Tremblay, Anthony D Okely","doi":"10.1016/s0140-6736(24)01389-8","DOIUrl":"https://doi.org/10.1016/s0140-6736(24)01389-8","url":null,"abstract":"Following the first 1000 days of life that span from conception to two years of age, the next 1000 days of a child's life from 2–5 years of age offer a window of opportunity to promote nurturing and caring environments, establish healthy behaviours, and build on early gains to sustain or improve trajectories of healthy development. This Series paper, the first of a two-paper Series on early childhood development and the next 1000 days, focuses on the transition to the next 1000 days of the life course, describes why this developmental period matters, identifies the environments of care, risks, and protective factors that shape children's development, estimates the number of children who receive adequate nurturing care, and examines whether current interventions are meeting children's needs. Paper 2 focuses on the cost of inaction and the implications of not investing in the next 1000 days. In low-income and middle-income countries (LMICs), only 62 million children aged 3 and 4 years (25·4%) currently receive adequate nurturing care during the next 1000 days, leaving 181·9 million children exposed to risks that jeopardise their healthy development. Inputs across nurturing care dimensions of health, nutrition, protection, responsive care, and learning vary substantially across countries. In LMICs, although 86·2% of children have a healthy weight in this period, less than one in three children have access to developmental stimulation or are protected from physical punishment, and only 38·8% have access to early childhood care and education services. Intervention research in LMICs in the next 1000 days is scarce. The continuity of developmentally appropriate nurturing care, coordination across health, education, and protection sectors, and the implementation of interventions to support caregivers and improve the quality of education and care remain top priorities in this period. These sectors play key roles in promoting quality early care and education for this age group, which will help maximise developmental potential and opportunities of children globally and help progress towards the achievement of the Sustainable Development Goals.","PeriodicalId":22898,"journal":{"name":"The Lancet","volume":"11 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142670824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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The Lancet
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