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Projected health and economic effects of a pan-tuberculosis treatment regimen: a modelling study. 泛结核病治疗方案对健康和经济的预期影响:模型研究。
IF 19.9 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 Epub Date: 2024-08-16 DOI: 10.1016/S2214-109X(24)00284-5
Theresa S Ryckman, C Finn McQuaid, Ted Cohen, Nicolas A Menzies, Emily A Kendall

Background: A pan-tuberculosis regimen that could be initiated without knowledge of drug susceptibility has been proposed as an objective of tuberculosis regimen development. We modelled the health and economic benefits of such a regimen and analysed which of its features contribute most to impact and savings.

Methods: We constructed a mathematical model of tuberculosis treatment parameterised with data from the published literature specific to three countries with a high tuberculosis burden (India, the Philippines, and South Africa). Our model simulated cohorts of newly diagnosed tuberculosis patients, including drug susceptibility testing if performed, regimen assignment, discontinuation, adherence, costs, and resulting outcomes of durable cure (microbiological cure without relapse), need for retreatment, or death. We compared a pan-tuberculosis regimen meeting the WHO 2023 target regimen profile against the standard of care of separate rifampicin-susceptible and rifampicin-resistant regimens. We estimated incremental cures; averted deaths, secondary cases, and costs; and prices below which a pan-tuberculosis regimen would be cost saving. We also assessed scenarios intended to describe which mechanisms of benefit from a pan-tuberculosis regimen (including improved characteristics compared with the current rifampicin-susceptible and rifampicin-resistant regimens and improved regimen assignment and retention in care for patients with rifampicin-resistant tuberculosis) would be most impactful. Results are presented as a range of means across countries with the most extreme 95% uncertainty intervals (UIs) from the three UI ranges.

Findings: Compared with the standard of care, a pan-tuberculosis regimen could increase the proportion of patients durably cured after an initial treatment attempt from 69-71% (95% UI 57-80) to 75-76% (68-83), preventing 30-32% of the deaths (20-43) and 17-20% of the transmission (9-29) that occur after initial tuberculosis diagnosis. Considering savings to the health system and patients during and after the initial treatment attempt, the regimen could reduce non-drug costs by 32-42% (22-49) and would be cost saving at prices below US$170-340 (130-510). A rifamycin-containing regimen that otherwise met pan-tuberculosis targets yielded only slightly less impact, indicating that most of the benefits from a pan-tuberculosis regimen resulted from its improvements upon the rifampicin-susceptible standard of care. Eliminating non-adherence and treatment discontinuation, for example via a long-acting injectable regimen, increased health impact and savings.

Interpretation: In countries with a high tuberculosis burden, a shorter, highly efficacious, safe, and tolerable regimen to treat all tuberculosis could yield substantial health improvements and savings.

Funding: Bill & Melinda Gates Foundation.

背景:作为结核病治疗方案开发的一个目标,提出了一种无需了解药物敏感性即可启动的泛结核病治疗方案。我们模拟了这种疗法的健康和经济效益,并分析了这种疗法的哪些特点最能产生影响和节省费用:方法:我们构建了一个结核病治疗数学模型,该模型的参数化数据来自已发表的文献,具体针对三个结核病负担较重的国家(印度、菲律宾和南非)。我们的模型模拟了新诊断的肺结核患者队列,包括药物敏感性测试(如果进行)、治疗方案分配、停药、坚持治疗、费用,以及持久治愈(微生物治愈且不复发)、需要再治疗或死亡的结果。我们比较了符合世界卫生组织 2023 年目标方案的泛结核病治疗方案与分别采用利福平敏感和利福平耐药治疗方案的标准治疗方案。我们估算了增量治愈率;避免的死亡人数、继发病例和成本;以及泛结核病治疗方案节省成本的价格。我们还评估了一些方案,旨在说明泛结核病治疗方案的哪种获益机制(包括与目前的利福平敏感和利福平耐药治疗方案相比,改善了治疗方案的特性,以及改善了利福平耐药结核病患者的治疗方案分配和保留率)最具影响力。结果以各国的平均值范围和三个平均值范围中最极端的 95% 不确定区间 (UI) 表示:与标准治疗相比,泛结核病治疗方案可将初次治疗后持久治愈的患者比例从 69%-71% (95% UI 57-80) 提高到 75%-76% (68-83),防止初次结核病诊断后 30%-32% 的死亡(20-43 例)和 17%-20% 的传播(9-29 例)。考虑到在初次治疗期间和之后为卫生系统和患者节省的费用,该疗法可将非药物成本降低 32-42%(22-49),如果价格低于 170-340 美元(130-510),则可节省成本。在其他方面达到泛结核病目标的含利福平治疗方案所产生的影响略低,这表明泛结核病治疗方案的大部分益处来自于对利福平敏感的标准治疗方案的改进。消除不坚持治疗和中断治疗的现象,例如通过长效注射疗法,可增加对健康的影响并节省开支:在结核病负担较重的国家,采用疗程短、疗效高、安全、可耐受的方案治疗所有结核病,可大幅改善健康状况并节省开支:比尔及梅林达-盖茨基金会。
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引用次数: 0
Respiratory syncytial virus infection among children younger than 2 years admitted to a paediatric intensive care unit with extended severe acute respiratory infection in ten Gavi-eligible countries: the RSV GOLD-ICU Network study. 十个符合 Gavi 资格的国家中因扩展性严重急性呼吸道感染而入住儿科重症监护病房的两岁以下儿童的呼吸道合胞病毒感染情况:RSV GOLD-ICU 网络研究。
IF 19.9 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 Epub Date: 2024-08-28 DOI: 10.1016/S2214-109X(24)00269-9

Background: Patient-level data on life-threatening respiratory syncytial virus (RSV) infection in children in low-income and lower-middle-income countries (LMICs) are scarce, and this scarcity might limit demand for RSV interventions in LMICs who rely on support from Gavi, the Vaccine Alliance. We aimed to describe the characteristics of RSV-positive children younger than 2 years who were admitted to paediatric intensive care units (PICUs) with extended severe acute respiratory infection (eSARI) in Gavi-eligible countries.

Methods: The RSV GOLD-ICU Network study is a 2-year prospective, multicountry, observational study of children younger than 2 years admitted to a PICU with eSARI. The study was conducted at 12 referral hospitals in Bolivia, Cameroon, The Gambia, Ghana, Haiti, Mozambique, Nepal, Nigeria, Sudan, and Tanzania. For comparison with a high-income country, patients were also included from two referral hospitals in the Netherlands. Children were eligible for inclusion if they were aged between 4 days and 2 years, admitted to a PICU, and met the WHO eSARI definition. RSV infection was confirmed within 72 h of PICU admission via a molecular point-of-care test at LMIC study sites and via a PCR test at the Dutch study sites. Clinical data were extracted from admission charts of patients; underlying conditions that were identified at admission were classified as comorbidities. Socioeconomic and demographic data were collected via a written, structured, parental questionnaire.

Findings: Between April 28, 2021, and Sept 30, 2023, we included 2118 children who were admitted to a PICU with eSARI in the ten participating countries. 614 (29·0%; range 23·0-38·2) of 2118 children tested positive for RSV and 608 were included in descriptive analyses as six medical files were lost at one study site and data could not be retrieved. Among all 608 children infected with RSV, 379 (62%) were male and 229 (38%) were female. Median age at testing was 3·0 months (IQR 1·3-7·7). 30 (5%) of 608 children died from RSV infection. RSV fatality occurred at seven of ten participating LMIC study sites and was highest in Tanzania (seven [27%] of 26 children). Median age at testing of children who died with RSV infection was 1·8 months (IQR 1·1-4·2).

Interpretation: To our knowledge, this is the first prospective, multicountry study reporting data from children admitted to a PICU with life-threatening RSV infection in Gavi-eligible countries. As there is no access to intensive care for most children in LMICs, RSV prevention is urgently needed.

Funding: Bill & Melinda Gates Foundation.

Translations: For the Arabic, Portuguese, Hausa and Nepali translations of the abstract see Supplementary Materials section.

背景:低收入和中低收入国家(LMICs)儿童感染危及生命的呼吸道合胞病毒(RSV)的患者水平数据很少,这种稀缺性可能会限制依赖疫苗联盟 Gavi 支持的中低收入国家对 RSV 干预措施的需求。我们旨在描述符合 Gavi 条件的国家中因严重急性呼吸道感染(eSARI)而入住儿科重症监护病房(PICU)的 2 岁以下 RSV 阳性儿童的特征:RSV GOLD-ICU 网络研究是一项为期 2 年的前瞻性多国观察研究,研究对象是因 eSARI 而入住 PICU 的 2 岁以下儿童。该研究在玻利维亚、喀麦隆、冈比亚、加纳、海地、莫桑比克、尼泊尔、尼日利亚、苏丹和坦桑尼亚的 12 家转诊医院进行。为了与高收入国家进行比较,还纳入了荷兰两家转诊医院的患者。年龄在 4 天至 2 岁之间、入住 PICU 并符合世界卫生组织 eSARI 定义的儿童均可纳入研究。在低收入和中等收入国家的研究地点,RSV 感染是在 PICU 入院后 72 小时内通过分子床旁检测确认的;在荷兰的研究地点,则是通过 PCR 检测确认的。从患者入院病历中提取临床数据;入院时确定的基础疾病被归类为合并症。社会经济和人口统计学数据通过书面、结构化的家长问卷收集:在 2021 年 4 月 28 日至 2023 年 9 月 30 日期间,我们纳入了十个参与国家中 2118 名因 eSARI 而入住 PICU 的儿童。2118 名儿童中有 614 名(29-0%;范围 23-0-38-2)RSV 检测呈阳性,其中 608 名儿童被纳入描述性分析,因为有一个研究地点丢失了六份医疗档案,无法检索数据。在所有 608 名感染 RSV 的儿童中,379 名(62%)为男性,229 名(38%)为女性。检测时的年龄中位数为 3-0 个月(IQR 1-3-7-7)。608 名儿童中有 30 人(5%)死于 RSV 感染。在 10 个低收入、中等收入国家的参与研究地点中,有 7 个出现了 RSV 死亡病例,其中坦桑尼亚的死亡病例最多(26 名儿童中有 7 名 [27%])。因感染 RSV 而死亡的儿童接受检测时的中位年龄为 1-8 个月(IQR 1-1-4-2):据我们所知,这是第一项前瞻性多国研究,报告了符合 Gavi 资格的国家中因感染危及生命的 RSV 而入住 PICU 的儿童的数据。由于大多数低收入国家的儿童无法获得重症监护,因此迫切需要预防 RSV:比尔及梅琳达-盖茨基金会:摘要的阿拉伯语、葡萄牙语、豪萨语和尼泊尔语译文见补充材料部分。
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引用次数: 0
Working with the news media for the greater good. 为更大的利益与新闻媒体合作。
IF 34.3 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 DOI: 10.1016/s2214-109x(24)00333-4
Joy Shu'aibu
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引用次数: 0
Assessing the effect of health system resources on HIV and tuberculosis programmes in Malawi: a modelling study. 评估马拉维卫生系统资源对艾滋病毒和结核病计划的影响:一项建模研究。
IF 34.3 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 DOI: 10.1016/s2214-109x(24)00259-6
Tara D Mangal,Sakshi Mohan,Timothy Colbourn,Joseph H Collins,Mathew Graham,Andreas Jahn,Eva Janoušková,Ines Li Lin,Robert Manning Smith,Emmanuel Mnjowe,Margherita Molaro,Tisungane E Mwenyenkulu,Dominic Nkhoma,Bingling She,Asif Tamuri,Paul Revill,Andrew N Phillips,Joseph Mfutso-Bengo,Timothy B Hallett
BACKGROUNDMalawi is progressing towards UNAIDS and WHO End TB Strategy targets to eliminate HIV/AIDS and tuberculosis. We aimed to assess the prospective effect of achieving these goals on the health and health system of the country and the influence of consumable constraints.METHODSIn this modelling study, we used the Thanzi la Onse (Health for All) model, which is an individual-based multi-disease simulation model that simulates HIV and tuberculosis transmission, alongside other diseases (eg, malaria, non-communicable diseases, and maternal diseases), and gates access to essential medicines according to empirical estimates of availability. The model integrates dynamic disease modelling with health system engagement behaviour, health system use, and capabilities (ie, personnel and consumables). We used 2018 data on the availability of HIV and tuberculosis consumables (for testing, treatment, and prevention) across all facility levels of the country to model three scenarios of HIV and tuberculosis programme scale-up from Jan 1, 2023, to Dec 31, 2033: a baseline scenario, when coverage remains static using existing consumable constraints; a constrained scenario, in which prioritised interventions are scaled up with fixed consumable constraints; and an unconstrained scenario, in which prioritised interventions are scaled up with maximum availability of all consumables related to HIV and tuberculosis care.FINDINGSWith uninterrupted medical supplies, in Malawi, we projected HIV and tuberculosis incidence to decrease to 26 (95% uncertainty interval [UI] 19-35) cases and 55 (23-74) cases per 100 000 person-years by 2033 (from 152 [98-195] cases and 123 [99-160] cases per 100 000 person-years in 2023), respectively, with programme scale-up, averting a total of 12·21 million (95% UI 11·39-14·16) disability-adjusted life-years. However, the effect was compromised by restricted access to key medicines, resulting in approximately 58 700 additional deaths (33 400 [95% UI 22 000-41 000] due to AIDS and 25 300 [19 300-30 400] due to tuberculosis) compared with the unconstrained scenario. Between 2023 and 2033, eliminating HIV treatment stockouts could avert an estimated 12 100 deaths compared with the baseline scenario, and improved access to tuberculosis prevention medications could prevent 5600 deaths in addition to those achieved through programme scale-up alone. With programme scale-up under the constrained scenario, consumable stockouts are projected to require an estimated 14·3 million extra patient-facing hours between 2023 and 2033, mostly from clinical or nursing staff, compared with the unconstrained scenario. In 2033, with enhanced screening, 188 000 (81%) of 232 900 individuals projected to present with active tuberculosis could start tuberculosis treatment within 2 weeks of initial presentation if all required consumables were available, but only 8600 (57%) of 15 100 presenting under the baseline scenario.INTERPRETATIONIgnoring frailties in the he
背景马拉维正在逐步实现联合国艾滋病规划署和世界卫生组织消除结核病战略的目标,即消灭艾滋病毒/艾滋病和结核病。在这项建模研究中,我们使用了 Thanzi la Onse(人人享有健康)模型,该模型是一个基于个人的多疾病模拟模型,可模拟艾滋病毒和结核病的传播,以及其他疾病(如疟疾、非传染性疾病和孕产妇疾病),并根据对可用性的经验估计来决定基本药物的获取。该模型将动态疾病建模与卫生系统参与行为、卫生系统使用和能力(即人员和消耗品)相结合。我们使用 2018 年全国各级医疗机构的艾滋病和结核病耗材(用于检测、治疗和预防)可用性数据,模拟了从 2023 年 1 月 1 日到 2033 年 12 月 31 日艾滋病和结核病计划扩展的三种情景:基线情景,即在现有消耗品限制条件下,覆盖范围保持不变;受限情景,即在固定消耗品限制条件下,扩大优先干预措施的规模;无限制情景,即在最大限度地提供与艾滋病毒和结核病护理相关的所有消耗品的情况下,扩大优先干预措施的规模。结果我们预测,在马拉维,如果医疗用品不间断供应,随着计划的扩大,到 2033 年,每 100 000 人年的艾滋病毒和结核病发病率将分别降至 26 例(95% 不确定区间 [UI] 19-35)和 55 例(23-74)(2023 年为每 100 000 人年 152 [98-195] 例和 123 [99-160] 例),总共可避免 1,200 万-2,100 万(95% 不确定区间 [UI] 11-39-14-16)个残疾调整寿命年。然而,由于关键药物的获取受到限制,与无限制情景相比,效果大打折扣,导致死亡人数增加约 58 700 人(艾滋病导致 33 400 人 [95% UI 22 000-41 000],结核病导致 25 300 人 [19 300-30 400])。在 2023 年至 2033 年期间,与基线情景相比,消除艾滋病毒治疗库存可避免约 12 100 例死亡,而改善结核病预防药物的获取可避免 5600 例死亡,这还不包括仅通过扩大方案规模实现的死亡。与无限制情景相比,在有限制情景下扩大计划规模后,预计 2023 年至 2033 年期间,消耗品缺货将需要额外的 1400 万至 300 万个面向患者的小时,其中大部分来自临床或护理人员。2033 年,在加强筛查的情况下,如果能获得所有必需的消耗品,预计 232 900 名活动性肺结核患者中的 188 000 人(81%)可在初次发病后 2 周内开始接受肺结核治疗,但在基线情景下,15 100 名患者中只有 8600 人(57%)可在初次发病后 2 周内开始接受肺结核治疗。在扩大项目规模的同时加强医疗系统至关重要,这将为人口健康带来更大的益处,同时减轻严重受限的医疗系统的压力。
{"title":"Assessing the effect of health system resources on HIV and tuberculosis programmes in Malawi: a modelling study.","authors":"Tara D Mangal,Sakshi Mohan,Timothy Colbourn,Joseph H Collins,Mathew Graham,Andreas Jahn,Eva Janoušková,Ines Li Lin,Robert Manning Smith,Emmanuel Mnjowe,Margherita Molaro,Tisungane E Mwenyenkulu,Dominic Nkhoma,Bingling She,Asif Tamuri,Paul Revill,Andrew N Phillips,Joseph Mfutso-Bengo,Timothy B Hallett","doi":"10.1016/s2214-109x(24)00259-6","DOIUrl":"https://doi.org/10.1016/s2214-109x(24)00259-6","url":null,"abstract":"BACKGROUNDMalawi is progressing towards UNAIDS and WHO End TB Strategy targets to eliminate HIV/AIDS and tuberculosis. We aimed to assess the prospective effect of achieving these goals on the health and health system of the country and the influence of consumable constraints.METHODSIn this modelling study, we used the Thanzi la Onse (Health for All) model, which is an individual-based multi-disease simulation model that simulates HIV and tuberculosis transmission, alongside other diseases (eg, malaria, non-communicable diseases, and maternal diseases), and gates access to essential medicines according to empirical estimates of availability. The model integrates dynamic disease modelling with health system engagement behaviour, health system use, and capabilities (ie, personnel and consumables). We used 2018 data on the availability of HIV and tuberculosis consumables (for testing, treatment, and prevention) across all facility levels of the country to model three scenarios of HIV and tuberculosis programme scale-up from Jan 1, 2023, to Dec 31, 2033: a baseline scenario, when coverage remains static using existing consumable constraints; a constrained scenario, in which prioritised interventions are scaled up with fixed consumable constraints; and an unconstrained scenario, in which prioritised interventions are scaled up with maximum availability of all consumables related to HIV and tuberculosis care.FINDINGSWith uninterrupted medical supplies, in Malawi, we projected HIV and tuberculosis incidence to decrease to 26 (95% uncertainty interval [UI] 19-35) cases and 55 (23-74) cases per 100 000 person-years by 2033 (from 152 [98-195] cases and 123 [99-160] cases per 100 000 person-years in 2023), respectively, with programme scale-up, averting a total of 12·21 million (95% UI 11·39-14·16) disability-adjusted life-years. However, the effect was compromised by restricted access to key medicines, resulting in approximately 58 700 additional deaths (33 400 [95% UI 22 000-41 000] due to AIDS and 25 300 [19 300-30 400] due to tuberculosis) compared with the unconstrained scenario. Between 2023 and 2033, eliminating HIV treatment stockouts could avert an estimated 12 100 deaths compared with the baseline scenario, and improved access to tuberculosis prevention medications could prevent 5600 deaths in addition to those achieved through programme scale-up alone. With programme scale-up under the constrained scenario, consumable stockouts are projected to require an estimated 14·3 million extra patient-facing hours between 2023 and 2033, mostly from clinical or nursing staff, compared with the unconstrained scenario. In 2033, with enhanced screening, 188 000 (81%) of 232 900 individuals projected to present with active tuberculosis could start tuberculosis treatment within 2 weeks of initial presentation if all required consumables were available, but only 8600 (57%) of 15 100 presenting under the baseline scenario.INTERPRETATIONIgnoring frailties in the he","PeriodicalId":48783,"journal":{"name":"Lancet Global Health","volume":"36 1","pages":"e1638-e1648"},"PeriodicalIF":34.3,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142275283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Access to highly effective long-acting RSV-monoclonal antibodies for children in LMICs-reducing global inequity. 为低收入国家儿童提供高效长效 RSV 单克隆抗体--减少全球不公平现象。
IF 19.9 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 Epub Date: 2024-07-24 DOI: 10.1016/S2214-109X(24)00258-4
Heather J Zar, Manuele Piccolis, Jonne Terstappen, Natalie I Mazur, Lobna Gaayeb, Sébastien Morin, Louis Bont
{"title":"Access to highly effective long-acting RSV-monoclonal antibodies for children in LMICs-reducing global inequity.","authors":"Heather J Zar, Manuele Piccolis, Jonne Terstappen, Natalie I Mazur, Lobna Gaayeb, Sébastien Morin, Louis Bont","doi":"10.1016/S2214-109X(24)00258-4","DOIUrl":"10.1016/S2214-109X(24)00258-4","url":null,"abstract":"","PeriodicalId":48783,"journal":{"name":"Lancet Global Health","volume":" ","pages":"e1582-e1583"},"PeriodicalIF":19.9,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141789585","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Access in the rare diseases landscape. 罕见病领域的可及性。
IF 34.3 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 DOI: 10.1016/s2214-109x(24)00341-3
Anneliene H Jonker,Maria Cavaller-Bellaubi,Yukiko Nishimura,David A Pearce
{"title":"Access in the rare diseases landscape.","authors":"Anneliene H Jonker,Maria Cavaller-Bellaubi,Yukiko Nishimura,David A Pearce","doi":"10.1016/s2214-109x(24)00341-3","DOIUrl":"https://doi.org/10.1016/s2214-109x(24)00341-3","url":null,"abstract":"","PeriodicalId":48783,"journal":{"name":"Lancet Global Health","volume":"21 1","pages":"e1587"},"PeriodicalIF":34.3,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142275284","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Africa should research the long-term sequelae of mpox. 非洲应研究水痘的长期后遗症。
IF 19.9 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 Epub Date: 2024-07-17 DOI: 10.1016/S2214-109X(24)00288-2
Allan Komakech, Brian Ngongheh Ajong, Danny Kalala, Nora Efire, Cris Kacita, Emmanuel Hasivirwe Vakaniaki, Jonathan Izudi, Laurens Liesenborghs, Nicaise Ndembi
{"title":"Africa should research the long-term sequelae of mpox.","authors":"Allan Komakech, Brian Ngongheh Ajong, Danny Kalala, Nora Efire, Cris Kacita, Emmanuel Hasivirwe Vakaniaki, Jonathan Izudi, Laurens Liesenborghs, Nicaise Ndembi","doi":"10.1016/S2214-109X(24)00288-2","DOIUrl":"10.1016/S2214-109X(24)00288-2","url":null,"abstract":"","PeriodicalId":48783,"journal":{"name":"Lancet Global Health","volume":" ","pages":"e1580-e1581"},"PeriodicalIF":19.9,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141735438","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Global estimation of dietary micronutrient inadequacies: a modelling analysis. 全球膳食微量营养素不足估算:模型分析。
IF 19.9 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 Epub Date: 2024-08-29 DOI: 10.1016/S2214-109X(24)00276-6
Simone Passarelli, Christopher M Free, Alon Shepon, Ty Beal, Carolina Batis, Christopher D Golden

Background: Inadequate micronutrient intakes and related deficiencies are a major challenge to global public health. Analyses over the past 10 years have assessed global micronutrient deficiencies and inadequate nutrient supplies, but there have been no global estimates of inadequate micronutrient intakes. We aimed to estimate the global prevalence of inadequate micronutrient intakes for 15 essential micronutrients and to identify dietary nutrient gaps in specific demographic groups and countries.

Methods: In this modelling analysis, we adopted a novel approach to estimating micronutrient intake, which accounts for the shape of a population's nutrient intake distribution and is based on dietary intake data from 31 countries. Using a globally harmonised set of age-specific and sex-specific nutrient requirements, we then applied these distributions to publicly available data from the Global Dietary Database on modelled median intakes of 15 micronutrients for 34 age-sex groups from 185 countries, to estimate the prevalence of inadequate nutrient intakes for 99·3% of the global population.

Findings: On the basis of estimates of nutrient intake from food (excluding fortification and supplementation), more than 5 billion people do not consume enough iodine (68% of the global population), vitamin E (67%), and calcium (66%). More than 4 billion people do not consume enough iron (65%), riboflavin (55%), folate (54%), and vitamin C (53%). Within the same country and age groups, estimated inadequate intakes were higher for women than for men for iodine, vitamin B12, iron, and selenium and higher for men than for women for magnesium, vitamin B6, zinc, vitamin C, vitamin A, thiamin, and niacin.

Interpretation: To our knowledge, this analysis provides the first global estimates of inadequate micronutrient intakes using dietary intake data, highlighting highly prevalent gaps across nutrients and variability by sex. These results can be used by public health practitioners to target populations in need of intervention.

Funding: The National Institutes of Health and the Dutch Ministry of Foreign Affairs.

背景:微量营养素摄入不足及相关缺乏症是全球公共卫生面临的一大挑战。过去 10 年的分析评估了全球微量营养素缺乏和营养素供应不足的情况,但还没有对全球微量营养素摄入不足的情况进行估计。我们旨在估算全球 15 种必需微量营养素摄入不足的普遍程度,并确定特定人口群体和国家的膳食营养素缺口:在这次建模分析中,我们采用了一种新方法来估算微量营养素摄入量,这种方法考虑到了人口营养素摄入量分布的形状,并以 31 个国家的膳食摄入量数据为基础。利用一套全球统一的特定年龄和性别营养素需求量,我们将这些分布应用于全球膳食数据库中关于185个国家34个年龄-性别组15种微量营养素摄入量模型中位数的公开数据,从而估算出全球99%-3%的人口营养素摄入不足的普遍程度:根据对食物中营养素摄入量的估计(不包括强化和补充),超过 50 亿人摄入的碘(占全球人口的 68%)、维生素 E(67%)和钙(66%)不足。超过 40 亿人没有摄入足够的铁(65%)、核黄素(55%)、叶酸(54%)和维生素 C(53%)。在同一国家和年龄组中,碘、维生素 B12、铁和硒的估计摄入不足率女性高于男性,镁、维生素 B6、锌、维生素 C、维生素 A、硫胺素和烟酸的估计摄入不足率男性高于女性:据我们所知,这项分析首次利用膳食摄入数据对全球微量营养素摄入不足的情况进行了估算,突出了各种营养素之间普遍存在的差距以及性别差异。公共卫生从业人员可利用这些结果来锁定需要干预的人群:美国国立卫生研究院和荷兰外交部。
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引用次数: 0
RSV burden and prevention in children in LMICs. 低收入国家儿童 RSV 负担和预防。
IF 19.9 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 Epub Date: 2024-08-28 DOI: 10.1016/S2214-109X(24)00289-4
Adam MacNeil, Meredith McMorrow
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引用次数: 0
What can we learn from developments in primary health care in south Asia? 我们能从南亚初级卫生保健的发展中学到什么?
IF 19.9 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2024-10-01 Epub Date: 2024-08-20 DOI: 10.1016/S2214-109X(24)00279-1
Radhika Gore, Stephanie M Topp, Maciej Banach, Onno C P van Schayck
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引用次数: 0
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Lancet Global Health
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