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The role of antibody-dependent enhancement in dengue vaccination. 抗体依赖性增强在登革热疫苗接种中的作用。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-11-01 DOI: 10.1186/s40794-024-00231-2
D G Aynekulu Mersha, I van der Sterren, L P M van Leeuwen, T Langerak, M S Hakim, B Martina, S F L van Lelyveld, E C M van Gorp

Dengue is the most rapidly spreading vector-borne disease worldwide, with over half the global population at risk for an infection. Antibody-dependent enhancement (ADE) is associated with increased disease severity and may also be attributable to the deterioration of disease in vaccinated people. Two dengue vaccines are approved momentarily, with more in development. The increasing use of vaccines against dengue, combined with the development of more, makes a thorough understanding of the processes behind ADE more important than ever. Above that, due to the lack of treatment options, this method of prevention is of great importance. This review aims to explore the impact of ADE in dengue vaccinations, with the goal of enhancing potential vaccination strategies in the fight against dengue.

登革热是全球传播最迅速的病媒传染病,全球有一半以上的人口面临感染风险。抗体依赖性增强(ADE)与疾病严重程度的增加有关,也可能是疫苗接种者病情恶化的原因。目前已有两种登革热疫苗获得批准,还有更多疫苗正在研发中。随着登革热疫苗的使用越来越多,以及更多疫苗的开发,彻底了解 ADE 背后的过程比以往任何时候都更加重要。此外,由于缺乏治疗方法,这种预防方法也非常重要。本综述旨在探讨 ADE 在登革热疫苗接种中的影响,目的是在对抗登革热的斗争中加强潜在的疫苗接种策略。
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引用次数: 0
Secreted protein NFA47630 from Nocardia farcinica IFM10152 induces immunoprotective effects in mice. 远古诺卡氏菌 IFM10152 的分泌蛋白 NFA47630 可诱导小鼠产生免疫保护作用。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-10-15 DOI: 10.1186/s40794-024-00229-w
Lichao Han, Xingzhao Ji, Shihong Fan, Jirao Shen, Bin Liang, Zhenjun Li

Purpose: Nocardia is emerging as a common and easily neglected cause of both healthcare- and occupation-associated infections worldwide, however, human vaccines for Nocardia prevention are not yet available. In this study, we aimed to evaluate the immunoprotective effect of the NFA47630 protein, a secreted protein abundant in the N. farcinica IFM10152 supernatant.

Methods: Conservation and characteristics of nfa47630 were analyzed by PCR and bioinformatics. Then recombinant NFA47630 protein was cloned, expressed and purified for further antigenicity analysis. Subsequently, the ability to activate innate immunity was evaluated by examining the phosphorylation status of the MAPK signaling pathway and cytokine levels. Finally, the protective effect was evaluated on rNFA47630-immunized mice.

Results: nfa47630 was conserved in N. farcinica strains with good antigenicity. The rNFA47630 protein was expressed under the optimal conditions of 0.2 mM IPTG, 28 °C, and it can be recognized by anti-N. farcinica and anti-N. cyriacigeorgica sera, but not anti-N. asteroids, anti-N. brasiliensis, anti-N. nova and anti-Mycobacterium bovis sera. It can upregulate the phosphorylation status of ERK, JNK, P38 and the cytokine levels of TNF-α, IL-10, IL-12, and IFN-γ. In addition, mice immunized with rNFA47630 protein exhibited higher antibody titers, greater bacterial clearance ability, milder organ infection, and higher survival rates than PBS-immunized mice.

Conclusions: Our data demonstrate that NFA47630 is a potential vaccine candidate for defending against N. farcinica infection.

目的:诺卡氏菌正在成为全球常见且易被忽视的医疗保健和职业相关感染的病因,但目前还没有用于预防诺卡氏菌的人类疫苗。本研究旨在评估 NFA47630 蛋白的免疫保护作用,NFA47630 蛋白是一种在 N. farcinica IFM10152 上清液中含量丰富的分泌蛋白:方法:通过 PCR 和生物信息学分析了 NFA47630 的保守性和特征。然后克隆、表达和纯化重组 NFA47630 蛋白,进一步进行抗原性分析。随后,通过检测 MAPK 信号通路的磷酸化状态和细胞因子水平来评估其激活先天性免疫的能力。最后,对rNFA47630免疫小鼠的保护作用进行了评估。rNFA47630蛋白在0.2 mM IPTG、28 °C的最佳条件下表达,能被抗N. farcinica和抗N. cyriacigeorgica血清识别,但不能被抗N. asteroids、抗N. brasiliensis、抗N. nova和抗牛分枝杆菌血清识别。它能上调 ERK、JNK、P38 的磷酸化状态以及 TNF-α、IL-10、IL-12 和 IFN-γ 等细胞因子的水平。此外,与PBS免疫小鼠相比,rNFA47630蛋白免疫小鼠表现出更高的抗体滴度、更强的细菌清除能力、更轻的器官感染以及更高的存活率:我们的数据表明,NFA47630是一种潜在的候选疫苗,可用于防御远华蓟马感染。
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引用次数: 0
Early intervention of 5% albumin shown superior control of vascular integrity and function compared to ringer's lactatein hospitalized adult with grade I & II Dengue hemorrhagic fever: a multicenter randomized controlled trial in Indonesia. 印度尼西亚一项多中心随机对照试验显示,与林格乳酸盐相比,5%白蛋白的早期干预能更好地控制血管完整性和功能。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.1186/s40794-024-00230-3
Rika Bur, Suhendro Suwarto, Herdiman Theodorus Pohan, Joedo Prihartono, Alida Roswita Harahap, Beti Ernawati Dewi, Mohamad Sadikin, Andhika Rachman, Hadi Yusuf

Background: Dengue virus remains a major public health problem with one of the hallmark pathologies is the vascular leakage caused by endothelial dysfunction which can lead to Dengue Hemorrhagic Fever (DHF) manifestation. In the status quo, no specific therapy has been discovered but rather heavily relies on judicious and frequent monitoring of intravenous fluids administration. The current guideline has discussed the roles of fluid therapy during the Dengue Shock Syndrome (DSS) stage, however, administration of early fluid intervention for DHF grade I and II remains uncharted territory. In addition, the choice and timing of colloid administration remains underexplored. As one of the widely available colloids, 5% albumin has known physiological properties that potentially minimize plasma leakage. Therefore, this study aimed to evaluate the benefit of early intervention of 5% albumin in adults with DHF in the hope of preventing the lethal progression to DSS and further, shorten the length of stay (LOS) for patients.

Methods: We conducted a multicenter, open-labeled, randomized controlled trial in Jakarta and Banten to compare the effect of early intervention with 5% albumin in adult patients with DHF compared to Ringer's Lactate (RL). Statistical analyses were conducted using unpaired t-test and Mann-Whitney for normally and abnormally distributed data respectively.

Results: Adult patients with a diagnosis of DHF grade I and II that being hospitalized to receive the early intervention of 5% albumin had significantly lower levels of hemoconcentration 4, 12, and 24 h (p = 0.002, 0.001, 0.003, respectively), higher platelet counts 4 h (p = 0.036), higher serum albumin levels 48 h (p = 0.036), lower proteinuria 24 and 48 h post-albumin administration (p < 0.001, < 0.001, respectively), and shorter LOS (p < 0.001) when compared to the RL group.

Conclusion: Early intervention of 5% albumin showed better control on vascular integrity and function compared to ringer lactate in hospitalized adults with grade I & II DHF, thus halting the progression of DHF into DSS and other related complications which leads to faster recovery and shorter length of stay.

Trial registration: The study was registered to www.

Clinicaltrial: gov with trial registration number NCT04076254, and registration date October 31st 2016.

背景:登革热病毒仍然是一个重大的公共卫生问题,其标志性病理之一是由内皮功能障碍引起的血管渗漏,可导致登革出血热(DHF)表现。目前,尚未发现特效疗法,而是严重依赖于对静脉输液进行明智而频繁的监测。现行指南讨论了在登革休克综合征(DSS)阶段进行输液治疗的作用,但对 I 级和 II 级 DHF 进行早期输液干预仍是未知领域。此外,胶体的选择和给药时机仍未得到充分探讨。作为广泛使用的胶体之一,5% 白蛋白具有已知的生理特性,可最大限度地减少血浆渗漏。因此,本研究旨在评估 5%白蛋白早期干预 DHF 成人患者的益处,希望能预防 DSS 的致命进展,并进一步缩短患者的住院时间(LOS):我们在雅加达和万丹开展了一项多中心、开放标签、随机对照试验,以比较在成人 DHF 患者中使用 5%白蛋白与林格乳酸盐(RL)进行早期干预的效果。对正态分布和异常分布的数据分别采用非配对 t 检验和 Mann-Whitney 进行统计分析:结果:确诊为 I 级和 II 级 DHF 的成人患者住院接受 5%白蛋白早期干预后,4、12 和 24 小时的血液浓缩水平明显降低(p = 0.002、0.001、0.003,分别为 0.002、0.001、0.003),4 小时的血小板计数升高(p = 0.036),48 小时的血清白蛋白水平升高(p = 0.036),白蛋白用药后 24 和 48 小时的蛋白尿水平降低(p 结论:5%白蛋白早期干预对 DHF 的治疗效果显著:与林格乳酸盐相比,5%白蛋白的早期干预能更好地控制 I 级和 II 级 DHF 住院成人的血管完整性和功能,从而阻止 DHF 演变为 DSS 及其他相关并发症,使患者更快康复并缩短住院时间:该研究已在 www.Clinicaltrial: gov 注册,试验注册号为 NCT04076254,注册日期为 2016 年 10 月 31 日。
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引用次数: 0
A post-marketing study to evaluate the safety and immunogenicity of a quadrivalent influenza split-virion vaccine in elderly people aged 60 years and older. 一项针对 60 岁及以上老年人的上市后研究,旨在评估四价流感病毒裂解疫苗的安全性和免疫原性。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-09-15 DOI: 10.1186/s40794-024-00228-x
Zengqiang Kou, Xiaoyu Li, Ti Liu, Bei Fan, Wenqi An, Wenjue An, Mingan Dang, Ke Zhang, Jingning Tang, Nan Zhu, Ruowen Pan

Background: Influenza remains a global public health concern. Understanding the vaccination-induced response in an aging population, which is susceptible and at high risk, is essential for disease prevention and control. Here, we report findings on the safety and immunogenicity of a quadrivalent influenza split-virion vaccine (15 µg/subtype/0.5 ml/dose) (hereinafter referred to as the "quadrivalent influenza vaccine") in a population aged ≥ 60 years.

Methods: This open-label, pragmatic post-marketing trial enrolled 1399 older adults to receive one dose of an approved commercially available quadrivalent influenza vaccine manufactured by Hualan Biological Bacterin Inc. (hereinafter referred to as "Hualan Bio"). Participants with contraindications for the vaccine were excluded, while poor health condition was acceptable. All vaccinated subjects experienced adverse events collection within 30 days and serious adverse events within 180 days post-vaccination. 25% subjects, selected randomly, underwent venous blood sampling pre-vaccination and 30 days after post-vaccination, for detecting antibody titers against each subtype of influenza virus by hemagglutination inhibition assay. The incidences of adverse events and antibody titers against each subtype of influenza virus were statistically analyzed using SAS 9.4.

Results: No grade 3 adverse reactions occurred within 30 days post-vaccination. The incidences of overall adverse reactions, local adverse reactions and systemic adverse reactions were 3.79%, 2.86% and 1.00%, respectively. No serious adverse reactions occurred within 180 days post-vaccination. There were 350 subjects who completed venous blood sampling pre-vaccination, among whom 348 subjects completed venous blood sampling at 30 days post-vaccination for immunogenicity assessment. With respect to hemagglutination inhibition antibodies against influenza viruses H1N1, H3N2, BV and BY subtypes, at 30 days post-vaccination, the seroconversion rates were 87.64%, 75.57%, 73.28% and 78.74%, respectively; the seropositive rates were 93.97%, 98.56%, 79.31% and 95.40%, respectively; and the geometric mean increase (GMI) in post-immunization/pre-immunization antibodies was 24.80, 7.26, 10.39 and 7.39, respectively.

Conclusion: One 15 µg/subtype dose of the vaccine had a good safety profile and elicited favorable immunogenicity among subjects aged ≥ 60 years. The results of this study indicate that Hualan Bio quadrivalent influenza vaccine strike balance between safety and immunogenicity, supporting unnecessity to increase dosage or inoculation frequency for further enhancing immunogenicity.

Trial registration: Registered on ClinicalTrials.gov.

Registration number: NCT06334510. Registered on 28/03/2024 (retrospectively registered).

背景:流感仍然是一个全球公共卫生问题。老龄人口是流感的易感人群和高危人群,了解他们对疫苗接种的反应对疾病的预防和控制至关重要。在此,我们报告了四价流感病毒裂解疫苗(15 µg/subtype/0.5 ml/剂量)(以下简称 "四价流感疫苗")在年龄≥ 60 岁人群中的安全性和免疫原性:这项开放标签、实用性的上市后试验招募了1399名老年人,让他们接种一剂由华兰生物菌素公司(以下简称 "华兰生物")生产的已获批准的市售四价流感疫苗。有疫苗接种禁忌症的受试者被排除在外,而健康状况较差的受试者则可以接受。所有接种对象均在接种后 30 天内出现不良反应,180 天内出现严重不良反应。随机抽取 25% 的受试者在接种前和接种后 30 天内进行静脉采血,通过血凝抑制试验检测各亚型流感病毒的抗体滴度。使用 SAS 9.4 对不良反应发生率和各亚型流感病毒抗体滴度进行了统计分析:接种后 30 天内未出现三级不良反应。总体不良反应、局部不良反应和全身不良反应的发生率分别为 3.79%、2.86% 和 1.00%。接种后 180 天内未发生严重不良反应。350名受试者在接种前完成了静脉采血,其中348名受试者在接种后30天完成了静脉采血,以进行免疫原性评估。接种后 30 天,受试者针对 H1N1、H3N2、BV 和 BY 亚型流感病毒的血凝抑制抗体的血清转换率分别为 87.64%、75.57%、73.28% 和 78.74%。74%;血清阳性率分别为 93.97%、98.56%、79.31% 和 95.40%;免疫后/免疫前抗体的几何平均增长(GMI)分别为 24.80、7.26、10.39 和 7.39:在年龄≥ 60 岁的受试者中,一剂 15 µg/subtype 疫苗具有良好的安全性和免疫原性。该研究结果表明,华兰生物四价流感疫苗在安全性和免疫原性之间取得了平衡,无需增加剂量或接种次数以进一步提高免疫原性:试验注册:已在 ClinicalTrials.gov 注册。注册号:NCT06334510:NCT06334510.注册日期:2024 年 3 月 28 日(回顾性注册)。
{"title":"A post-marketing study to evaluate the safety and immunogenicity of a quadrivalent influenza split-virion vaccine in elderly people aged 60 years and older.","authors":"Zengqiang Kou, Xiaoyu Li, Ti Liu, Bei Fan, Wenqi An, Wenjue An, Mingan Dang, Ke Zhang, Jingning Tang, Nan Zhu, Ruowen Pan","doi":"10.1186/s40794-024-00228-x","DOIUrl":"https://doi.org/10.1186/s40794-024-00228-x","url":null,"abstract":"<p><strong>Background: </strong>Influenza remains a global public health concern. Understanding the vaccination-induced response in an aging population, which is susceptible and at high risk, is essential for disease prevention and control. Here, we report findings on the safety and immunogenicity of a quadrivalent influenza split-virion vaccine (15 µg/subtype/0.5 ml/dose) (hereinafter referred to as the \"quadrivalent influenza vaccine\") in a population aged ≥ 60 years.</p><p><strong>Methods: </strong>This open-label, pragmatic post-marketing trial enrolled 1399 older adults to receive one dose of an approved commercially available quadrivalent influenza vaccine manufactured by Hualan Biological Bacterin Inc. (hereinafter referred to as \"Hualan Bio\"). Participants with contraindications for the vaccine were excluded, while poor health condition was acceptable. All vaccinated subjects experienced adverse events collection within 30 days and serious adverse events within 180 days post-vaccination. 25% subjects, selected randomly, underwent venous blood sampling pre-vaccination and 30 days after post-vaccination, for detecting antibody titers against each subtype of influenza virus by hemagglutination inhibition assay. The incidences of adverse events and antibody titers against each subtype of influenza virus were statistically analyzed using SAS 9.4.</p><p><strong>Results: </strong>No grade 3 adverse reactions occurred within 30 days post-vaccination. The incidences of overall adverse reactions, local adverse reactions and systemic adverse reactions were 3.79%, 2.86% and 1.00%, respectively. No serious adverse reactions occurred within 180 days post-vaccination. There were 350 subjects who completed venous blood sampling pre-vaccination, among whom 348 subjects completed venous blood sampling at 30 days post-vaccination for immunogenicity assessment. With respect to hemagglutination inhibition antibodies against influenza viruses H1N1, H3N2, BV and BY subtypes, at 30 days post-vaccination, the seroconversion rates were 87.64%, 75.57%, 73.28% and 78.74%, respectively; the seropositive rates were 93.97%, 98.56%, 79.31% and 95.40%, respectively; and the geometric mean increase (GMI) in post-immunization/pre-immunization antibodies was 24.80, 7.26, 10.39 and 7.39, respectively.</p><p><strong>Conclusion: </strong>One 15 µg/subtype dose of the vaccine had a good safety profile and elicited favorable immunogenicity among subjects aged ≥ 60 years. The results of this study indicate that Hualan Bio quadrivalent influenza vaccine strike balance between safety and immunogenicity, supporting unnecessity to increase dosage or inoculation frequency for further enhancing immunogenicity.</p><p><strong>Trial registration: </strong>Registered on ClinicalTrials.gov.</p><p><strong>Registration number: </strong>NCT06334510. Registered on 28/03/2024 (retrospectively registered).</p>","PeriodicalId":23303,"journal":{"name":"Tropical Diseases, Travel Medicine and Vaccines","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11402193/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142296300","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cardioembolic stroke in Chagas disease: unraveling the underexplored connection through a systematic review. 南美锥虫病引发的心栓塞性中风:通过系统回顾揭示未充分探索的关联。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-09-01 DOI: 10.1186/s40794-024-00227-y
Jorge Vásconez-González, Camila Miño, Juan S Izquierdo-Condoy, Camila Salazar-Santoliva, Andrés López-Cortés, Esteban Ortiz-Prado

Background: Chagas disease (CD), triggered by the Trypanosoma cruzi parasite, is originally endemic across Latin America, affecting millions. While cardiac complications are widely recognized, the association between CD and stroke remains underexplored. This systematic review aims to elucidate the relationship between CD and stroke, highlighting the cardioembolic origins of stroke in CD patients and assessing the elevated stroke risk compared to non-infected individuals.

Methodology: Adhering to the PRISMA guidelines, we conducted a comprehensive search in PubMed and Scopus databases without date restrictions, including articles in both Spanish and English. This approach enabled the identification and analysis of relevant studies to understand the interplay between CD and stroke risk.

Results: Our analysis of 25 selected studies indicates that strokes in CD patients predominantly arise from cardioembolic sources. The data underscore a significant increase in stroke risk among individuals infected with T. cruzi compared to uninfected counterparts. Additionally, CD patients face a higher stroke and mortality risk than those with other heart failure etiologies, irrespective of disease severity.

Conclusion: The review establishes CD as a critical contributor to stroke incidence, emphasizing the need for heightened awareness and diagnosis of CD in stroke patients, particularly in regions with high CD prevalence. Recognizing the increased stroke risk associated with T. cruzi infection is crucial for developing targeted educational and preventive strategies in endemic areas.

背景:南美锥虫病(CD)是由南美锥虫引发的,最初在拉丁美洲流行,影响数百万人。虽然心脏并发症已被广泛认识,但 CD 与中风之间的关系仍未得到充分探讨。本系统综述旨在阐明 CD 与中风之间的关系,强调 CD 患者中风的心栓塞起源,并评估与未感染者相比中风风险的升高:根据 PRISMA 指南,我们在 PubMed 和 Scopus 数据库中进行了全面搜索,没有日期限制,包括西班牙语和英语文章。这种方法有助于识别和分析相关研究,以了解 CD 与中风风险之间的相互作用:结果:我们对所选的 25 项研究进行的分析表明,CD 患者的中风主要源于心肌栓塞。这些数据表明,与未感染的同类患者相比,感染了 T. cruzi 的患者中风风险明显增加。此外,与其他心衰病因的患者相比,无论疾病严重程度如何,CD 患者都面临着更高的中风和死亡风险:本综述将 CD 定义为中风发病率的一个重要因素,强调需要提高中风患者对 CD 的认识和诊断,尤其是在 CD 高发地区。认识到与 T. cruzi 感染相关的中风风险增加对于在疾病流行地区制定有针对性的教育和预防策略至关重要。
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引用次数: 0
Travellers with prosthetic limbs, a neglected population. A perspective on what travel health practitioners need to know. 装有假肢的旅行者,一个被忽视的群体。从旅行保健从业人员需要了解的角度出发。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-08-15 DOI: 10.1186/s40794-024-00226-z
Irmgard L Bauer, Vikranth H Nagaraja

Background: The benefits of travel for the wellbeing of people of all ages and abilities are well known, though travellers with prostheses have so far been excluded. Limb loss, due to trauma, vascular disease, cancer, or infections requires a prosthesis for cosmesis and functionality. The life-changing event of losing a limb and the considerable psychological adjustment to accept an altered body image influence rehabilitation and self-management as well as the participation in social activities, such as sport and travel. The challenge of travel lies not only in transferring practical impediments encountered at home to another location; familiar coping strategies may require unexpected adjustments. After presenting background information on limb loss and prostheses, the purpose of this paper was to review literature on health advice for travellers with prosthetic limbs.

Method: All major data bases were searched for peer-reviewed literature using a variation of keyword combinations around travel and prosthetics. Relevant journals were searched individually, and selected authors and university departments contacted. No evidence-based results were obtained. The search then moved to grey literature including documents from relevant organisations, professional bodies, government websites, manufacturers, airlines, prosthetic/physiotherapy clinics, sport organisations to approaching amputees, including veterans and athletes, directly.

Result: The list of collated travel advice for people with artificial limbs relates to (1) trip preparation, (2) packing (especially considering the mechanical and/or electrical requirements of the prosthesis), (3) travelling by plane as the most covered mode of travel, and (4) navigating airports and airport security, which may be used by travel health practitioners while awaiting evidence-based guidelines.

Conclusion: This is the first paper on travel with a prosthetic limb in any field, including travel medicine. Therefore, travel health practitioners have no evidence-based guidelines at their disposal required for high-quality care for this neglected population. Preliminary recommendations for clinical practice, advice for required updates in education, and suggestions for urgently needed research are provided to replace current hints and tips with evidence so that travellers with prostheses are no longer 'out on a limb'.

背景:众所周知,旅行对不同年龄、不同能力的人都有好处,但装有假肢的旅行者至今仍被排除在外。由于外伤、血管疾病、癌症或感染导致的肢体缺失,需要安装假肢来保持外观和功能。失去肢体这一改变生活的事件,以及接受身体形象改变所带来的巨大心理调整,都会影响康复和自我管理,以及参与体育和旅行等社会活动。旅行的挑战不仅在于将在家中遇到的实际障碍转移到另一个地方,熟悉的应对策略也可能需要做出意想不到的调整。在介绍了有关肢体缺失和假肢的背景信息后,本文旨在回顾有关为携带假肢的旅行者提供健康建议的文献:方法:使用围绕旅行和假肢的不同关键词组合,在所有主要数据库中搜索同行评审文献。对相关期刊进行了逐一检索,并联系了部分作者和大学院系。未获得任何基于证据的结果。然后转而搜索灰色文献,包括相关组织、专业机构、政府网站、制造商、航空公司、假肢/物理治疗诊所、体育组织的文件,以直接接触截肢者,包括退伍军人和运动员:整理出的假肢使用者旅行建议清单涉及:(1) 旅行准备;(2) 包装(特别是考虑到假肢的机械和/或电气要求);(3) 乘飞机旅行是最常见的旅行方式;(4) 机场和机场安检导航,旅行保健从业人员可在等待循证指南时使用这些建议:结论:这是第一篇关于在任何领域(包括旅行医学)携带假肢旅行的论文。因此,旅行医疗从业人员还没有为这一被忽视的人群提供高质量医疗服务所需的循证指南。本文对临床实践提出了初步建议,对教育中需要更新的内容提出了建议,并对急需开展的研究提出了建议,以便用证据来取代目前的提示和窍门,使携带假肢的旅行者不再 "束手无策"。
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引用次数: 0
A landscape review of malaria vaccine candidates in the pipeline. 疟疾疫苗候选项目概览。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-08-01 DOI: 10.1186/s40794-024-00222-3
Yusuf Amuda Tajudeen, Habeebullah Jayeola Oladipo, Sodiq Inaolaji Yusuff, Samuel O Abimbola, Muritala Abdulkadir, Iyiola Olatunji Oladunjoye, Abass Olawale Omotosho, Oluwaseyi Muyiwa Egbewande, Hameedat Damilola Shittu, Rashidat Onyinoyi Yusuf, Oluwatosin Ogundipe, Abdulbasit Opeyemi Muili, Abdullateef Opeyemi Afolabi, Salwa M A Dahesh, Marwa Ahmed Mahmoud Gameil, Mona Said El-Sherbini

Background: Globally, malaria continues to pose a major health challenge, with approximately 247 million cases of the illness and 627,000 deaths reported in 2021. However, the threat is particularly pronounced in sub-Saharan African countries, where pregnant women and children under the age of five face heightened vulnerability to the disease. As a result, the imperative to develop malaria vaccines especially for these vulnerable populations, remains crucial in the pursuit of malaria eradication. However, despite decades of research, effective vaccine development faces technical challenges, including the rapid spread of drug-resistant parasite strains, the complex parasite lifecycle, the development of liver hypnozoites with potential for relapse, and evasion of the host immune system. This review aims to discuss the different malaria vaccine candidates in the pipeline, highlighting different approaches used for adjuvating these candidates, their benefits, and outcomes, and summarizing the progress of these vaccine candidates under development.

Method: A comprehensive web-based search for peer-reviewed journal articles published in SCOPUS, MEDLINE (via PubMed), Science Direct, WHO, and Advanced Google Scholar databases was conducted from 1990 to May 2022. Context-specific keywords such as "Malaria", "Malaria Vaccine", "Malaria Vaccine Candidates", "Vaccine Development", "Vaccine Safety", "Clinical Trials", "mRNA Vaccines", "Viral Vector Vaccines", "Protein-based Vaccines", "Subunit Vaccines", "Vaccine Adjuvants", "Vaccine-induced Immune Responses", and "Immunogenicity" were emphatically considered. Articles not directly related to malaria vaccine candidates in preclinical and clinical stages of development were excluded.

Results: Various approaches have been studied for malaria vaccine development, targeting different parasite lifecycle stages, including the pre-erythrocytic, erythrocytic, and sexual stages. The RTS, S/AS01 vaccine, the first human parasite vaccine reaching WHO-listed authority maturity level 4, has demonstrated efficacy in preventing clinical malaria in African children. However, progress was slow in introducing other safe, and feasible malaria vaccines through clinical trials . Recent studies highlight the potential effectiveness of combining pre-erythrocytic and blood-stage vaccines, along with the advantages of mRNA vaccines for prophylaxis and treatment, and nonstructural vaccines for large-scale production.

Conclusion: Malaria vaccine candidates targeting different lifecycle stages of the parasite range from chemoprophylaxis vaccination to cross-species immune protection. The use of a multi-antigen, multi-stage combinational vaccine is therefore essential in the context of global health. This demands careful understanding and critical consideration of the long-term multi-faceted interplay of immune interference, co-dominance, complement

背景:在全球范围内,疟疾仍然是一项重大的健康挑战,2021 年报告的疟疾病例约为 2.47 亿例,627,000 人死亡。然而,这一威胁在撒哈拉以南非洲国家尤为明显,那里的孕妇和五岁以下儿童更容易感染疟疾。因此,开发疟疾疫苗,尤其是针对这些易感人群的疫苗,对于根除疟疾仍然至关重要。然而,尽管进行了数十年的研究,有效的疫苗开发仍面临着技术挑战,包括抗药性寄生虫菌株的快速传播、寄生虫复杂的生命周期、具有复发潜力的肝脏下吸虫的发育以及宿主免疫系统的逃避。本综述旨在讨论不同的候选疟疾疫苗,重点介绍用于佐剂这些候选疫苗的不同方法、其益处和结果,并总结这些候选疫苗的研发进展:方法:对 1990 年至 2022 年 5 月期间在 SCOPUS、MEDLINE(通过 PubMed)、Science Direct、WHO 和高级 Google Scholar 数据库中发表的同行评审期刊论文进行了全面的网络检索。重点考虑了 "疟疾"、"疟疾疫苗"、"候选疟疾疫苗"、"疫苗开发"、"疫苗安全性"、"临床试验"、"mRNA 疫苗"、"病毒载体疫苗"、"蛋白质疫苗"、"亚单位疫苗"、"疫苗佐剂"、"疫苗诱导的免疫反应 "和 "免疫原性 "等特定关键词。与处于临床前和临床开发阶段的候选疟疾疫苗没有直接关系的文章被排除在外:针对不同的寄生虫生命周期阶段,包括前红细胞期、红细胞期和性阶段,人们研究了多种疟疾疫苗开发方法。RTS、S/AS01 疫苗是首个达到世卫组织所列权威成熟度 4 级的人类寄生虫疫苗,在预防非洲儿童临床疟疾方面已证明有效。然而,在通过临床试验引入其他安全可行的疟疾疫苗方面进展缓慢。最近的研究强调了将红细胞前期疫苗和血期疫苗相结合的潜在有效性,以及用于预防和治疗的 mRNA 疫苗和用于大规模生产的非结构疫苗的优势:结论:针对寄生虫不同生命周期阶段的疟疾疫苗候选方案包括从化学预防接种到跨物种免疫保护。因此,在全球健康背景下,使用多抗原、多阶段组合疫苗至关重要。这就需要仔细了解和认真考虑影响疫苗诱导的整体免疫反应的免疫干扰、共支配、互补免疫反应、分子靶点和佐剂等多方面的长期相互作用。尽管存在挑战,但临床试验和疫苗接种技术的进步为疟疾疫苗开发的新方法提供了充满希望的可能性。
{"title":"A landscape review of malaria vaccine candidates in the pipeline.","authors":"Yusuf Amuda Tajudeen, Habeebullah Jayeola Oladipo, Sodiq Inaolaji Yusuff, Samuel O Abimbola, Muritala Abdulkadir, Iyiola Olatunji Oladunjoye, Abass Olawale Omotosho, Oluwaseyi Muyiwa Egbewande, Hameedat Damilola Shittu, Rashidat Onyinoyi Yusuf, Oluwatosin Ogundipe, Abdulbasit Opeyemi Muili, Abdullateef Opeyemi Afolabi, Salwa M A Dahesh, Marwa Ahmed Mahmoud Gameil, Mona Said El-Sherbini","doi":"10.1186/s40794-024-00222-3","DOIUrl":"10.1186/s40794-024-00222-3","url":null,"abstract":"<p><strong>Background: </strong>Globally, malaria continues to pose a major health challenge, with approximately 247 million cases of the illness and 627,000 deaths reported in 2021. However, the threat is particularly pronounced in sub-Saharan African countries, where pregnant women and children under the age of five face heightened vulnerability to the disease. As a result, the imperative to develop malaria vaccines especially for these vulnerable populations, remains crucial in the pursuit of malaria eradication. However, despite decades of research, effective vaccine development faces technical challenges, including the rapid spread of drug-resistant parasite strains, the complex parasite lifecycle, the development of liver hypnozoites with potential for relapse, and evasion of the host immune system. This review aims to discuss the different malaria vaccine candidates in the pipeline, highlighting different approaches used for adjuvating these candidates, their benefits, and outcomes, and summarizing the progress of these vaccine candidates under development.</p><p><strong>Method: </strong>A comprehensive web-based search for peer-reviewed journal articles published in SCOPUS, MEDLINE (via PubMed), Science Direct, WHO, and Advanced Google Scholar databases was conducted from 1990 to May 2022. Context-specific keywords such as \"Malaria\", \"Malaria Vaccine\", \"Malaria Vaccine Candidates\", \"Vaccine Development\", \"Vaccine Safety\", \"Clinical Trials\", \"mRNA Vaccines\", \"Viral Vector Vaccines\", \"Protein-based Vaccines\", \"Subunit Vaccines\", \"Vaccine Adjuvants\", \"Vaccine-induced Immune Responses\", and \"Immunogenicity\" were emphatically considered. Articles not directly related to malaria vaccine candidates in preclinical and clinical stages of development were excluded.</p><p><strong>Results: </strong>Various approaches have been studied for malaria vaccine development, targeting different parasite lifecycle stages, including the pre-erythrocytic, erythrocytic, and sexual stages. The RTS, S/AS01 vaccine, the first human parasite vaccine reaching WHO-listed authority maturity level 4, has demonstrated efficacy in preventing clinical malaria in African children. However, progress was slow in introducing other safe, and feasible malaria vaccines through clinical trials . Recent studies highlight the potential effectiveness of combining pre-erythrocytic and blood-stage vaccines, along with the advantages of mRNA vaccines for prophylaxis and treatment, and nonstructural vaccines for large-scale production.</p><p><strong>Conclusion: </strong>Malaria vaccine candidates targeting different lifecycle stages of the parasite range from chemoprophylaxis vaccination to cross-species immune protection. The use of a multi-antigen, multi-stage combinational vaccine is therefore essential in the context of global health. This demands careful understanding and critical consideration of the long-term multi-faceted interplay of immune interference, co-dominance, complement","PeriodicalId":23303,"journal":{"name":"Tropical Diseases, Travel Medicine and Vaccines","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11293096/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141861040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Characterizing zero-dose and under-vaccinated children among refugees and internally displaced persons in the Democratic Republic of Congo. 刚果民主共和国难民和境内流离失所者中接种疫苗次数为零和不足的儿童的特征。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-07-15 DOI: 10.1186/s40794-024-00225-0
Marcellin Mengouo Nimpa, Aimé Cikomola Mwana-Wabene, John Otomba, Jean-Crispin Mukendi, M Carolina Danovaro-Holliday, Franck-Fortune Mboussou, Dieudonné Mwamba, Leandre Kambala, Dolla Ngwanga, Cedric Mwanga, Sume Gerald Etapelong, Issaka Compaoré, Moise Désiré Yapi, Daniel Katuashi Ishoso

Background: The Democratic Republic of Congo (DRC) has one of the highest numbers of un and under-vaccinated children as well as number of refugees and internally displaced persons (IDPs) in the world. This study aims to determine and compare the proportion and characteristics of zero-dose (ZD) and under-vaccinated (UV) children among refugees and IDPs in the DRC, as well as the reasons for incomplete vaccination schedules.

Methods: Data from a rolling vaccination coverage survey conducted from September 10, 2022, to July 03, 2023, among refugees and IDPs in 12 provinces of the DRC. ZD was defined as a child aged 12-23 months who had not received any dose of pentavalent vaccine DTP-Hib-Hep B (by card or recall) and UV as a child who had not received the third dose of pentavalent vaccine. The proportions of non and under-vaccination and the associated factors using a logistic regression model are presented for ZD and UV children. The reasons for non-vaccination of these children are described using the WHO-Immunization behavioral and social-drivers-conceptual framework and compared using Pearson's Chi2 test.

Results: Of 692 children aged 12 to 23 months included in the analysis, 9.3% (95% CI: 7.2-11.7%) were ZD and 40.9% (95% CI: 95%: 37.2-44.6%) UV. The Penta1/Penta3 drop-out rate was 34.9%. After adjustment, ZD children had a significant history of home or road birth. And UV children were significantly associated with mothers/caregivers being under 40, uneducated, farmers, ranchers, employed, rural residents, as well as with home or road births. Reasons linked to people's perceptions and feelings were cited much more often for ZD (50.0%) than for UV (38.3%). Those related to social reasons were cited much more often by ZD (40.6%) than by UV (35.7%). Reasons related to "programmatic and practical issues" were cited less for ZD (90.5%) than for UV (97.1%).

Conclusions: ZD and UV children represent significant proportions in refugee and IDPs sites in the DRC. However, the proportion of ZD is less than for the entire country, while the proportion of UV is comparable, reflected in a very high drop-out rate. Similarly to studies in the general population in DRC, the reasons for ZD children were mainly linked to challenges in caregiver motivation to vaccinate, while for UV children, they were more often linked to pro-grammatic and practical problems of the health system.

背景:刚果民主共和国(DRC)是世界上未接种疫苗和接种疫苗不足的儿童人数最多的国家之一,同时也是难民和境内流离失所者(IDP)人数最多的国家之一。本研究旨在确定和比较刚果(金)难民和国内流离失所者中零剂量(ZD)和接种不足(UV)儿童的比例和特征,以及疫苗接种计划不完整的原因:数据来自 2022 年 9 月 10 日至 2023 年 7 月 3 日对刚果民主共和国 12 个省的难民和境内流离失所者进行的滚动疫苗接种覆盖率调查。未接种ZD是指12-23个月的儿童未接种过任何剂量的五价疫苗白喉-百日咳-破伤风-乙肝(通过卡或召回),未接种UV是指未接种过第三剂五价疫苗。本报告采用逻辑回归模型列出了未接种和接种不足的比例以及与之相关的因素。使用世界卫生组织免疫行为和社会驱动因素概念框架描述了这些儿童未接种疫苗的原因,并使用 Pearson's Chi2 检验进行了比较:在纳入分析的 692 名 12 至 23 个月大的儿童中,9.3%(95% CI:7.2-11.7%)为 ZD,40.9%(95% CI:95%:37.2-44.6%)为 UV。Penta1/Penta3的辍学率为34.9%。经调整后,ZD 儿童有明显的家庭或道路分娩史。尿毒症患儿的母亲/照顾者年龄在 40 岁以下、未受过教育、农民、牧场主、受雇者、农村居民,以及在家或路上分娩都与尿毒症有关。与人们的看法和感受有关的原因在浙大(50.0%)比在紫外(38.3%)更常被提及。与社会原因有关的原因,ZD(40.6%)比 UV(35.7%)更多。与 "计划和实际问题 "有关的原因,零起点儿童(90.5%)的提及率低于普通儿童(97.1%):结论:在刚果(金)的难民和境内流离失所者营地中,ZD儿童和UV儿童占很大比例。结论:在刚果(金)的难民和境内流离失所者营地中,ZD 和 UV 儿童所占比例很大,但 ZD 儿童的比例低于全国儿童,而 UV 儿童的比例与全国儿童相当,这反映在极高的辍学率上。与对刚果(金)普通人群的研究类似,零接种儿童辍种的原因主要与照顾者接种疫苗的积极性有关,而未接种儿童辍种的原因则更多地与卫生系统的计划和实际问题有关。
{"title":"Characterizing zero-dose and under-vaccinated children among refugees and internally displaced persons in the Democratic Republic of Congo.","authors":"Marcellin Mengouo Nimpa, Aimé Cikomola Mwana-Wabene, John Otomba, Jean-Crispin Mukendi, M Carolina Danovaro-Holliday, Franck-Fortune Mboussou, Dieudonné Mwamba, Leandre Kambala, Dolla Ngwanga, Cedric Mwanga, Sume Gerald Etapelong, Issaka Compaoré, Moise Désiré Yapi, Daniel Katuashi Ishoso","doi":"10.1186/s40794-024-00225-0","DOIUrl":"10.1186/s40794-024-00225-0","url":null,"abstract":"<p><strong>Background: </strong>The Democratic Republic of Congo (DRC) has one of the highest numbers of un and under-vaccinated children as well as number of refugees and internally displaced persons (IDPs) in the world. This study aims to determine and compare the proportion and characteristics of zero-dose (ZD) and under-vaccinated (UV) children among refugees and IDPs in the DRC, as well as the reasons for incomplete vaccination schedules.</p><p><strong>Methods: </strong>Data from a rolling vaccination coverage survey conducted from September 10, 2022, to July 03, 2023, among refugees and IDPs in 12 provinces of the DRC. ZD was defined as a child aged 12-23 months who had not received any dose of pentavalent vaccine DTP-Hib-Hep B (by card or recall) and UV as a child who had not received the third dose of pentavalent vaccine. The proportions of non and under-vaccination and the associated factors using a logistic regression model are presented for ZD and UV children. The reasons for non-vaccination of these children are described using the WHO-Immunization behavioral and social-drivers-conceptual framework and compared using Pearson's Chi2 test.</p><p><strong>Results: </strong>Of 692 children aged 12 to 23 months included in the analysis, 9.3% (95% CI: 7.2-11.7%) were ZD and 40.9% (95% CI: 95%: 37.2-44.6%) UV. The Penta1/Penta3 drop-out rate was 34.9%. After adjustment, ZD children had a significant history of home or road birth. And UV children were significantly associated with mothers/caregivers being under 40, uneducated, farmers, ranchers, employed, rural residents, as well as with home or road births. Reasons linked to people's perceptions and feelings were cited much more often for ZD (50.0%) than for UV (38.3%). Those related to social reasons were cited much more often by ZD (40.6%) than by UV (35.7%). Reasons related to \"programmatic and practical issues\" were cited less for ZD (90.5%) than for UV (97.1%).</p><p><strong>Conclusions: </strong>ZD and UV children represent significant proportions in refugee and IDPs sites in the DRC. However, the proportion of ZD is less than for the entire country, while the proportion of UV is comparable, reflected in a very high drop-out rate. Similarly to studies in the general population in DRC, the reasons for ZD children were mainly linked to challenges in caregiver motivation to vaccinate, while for UV children, they were more often linked to pro-grammatic and practical problems of the health system.</p>","PeriodicalId":23303,"journal":{"name":"Tropical Diseases, Travel Medicine and Vaccines","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11247746/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141617136","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Trend of pulmonary tuberculosis and rifampicin-resistance among tuberculosis presumptive patients in Central Tigray, Ethiopia; 2018 -2023: a six-year retrospective study. 2018-2023年埃塞俄比亚提格雷中部肺结核推定患者的肺结核和利福平耐药性趋势:一项为期六年的回顾性研究。
IF 2.4 Q3 INFECTIOUS DISEASES Pub Date : 2024-07-01 DOI: 10.1186/s40794-024-00224-1
Guesh Gebremariam, Mulugeta Kiros, Selemun Hagos, Haftom Hadush, Amaha Gebremichael, Gebretsadkan Gebrekirstos, Aregawi Tesfay, Teumelsan Gebrewahid, Tesfay Berihu, Brhane Gebremariam

Background: Tuberculosis (TB) is a major public health concern in the developing countries. Moreover, the emergence of multidrug-resistant tuberculosis is challenging. However, there are no organized data on the trends of pulmonary tuberculosis and rifampicin-resistant Mycobacterium tuberculosis in the study area.

Methods: A retrospective cross-sectional study was conducted to fill the information gap in Central Tigray at St. Mary General Hospital between 2018 and 2023. Data were collected from the GeneXpert™ tuberculosis registration logbooks using standard checklists and analyzed using Statistical Package for Social Science version 22. After performing logistic regression, a p-value < 0.05 with a corresponding 95% confidence interval was considered statistically significant. Moreover, chi square test for trend was performed to assess the percentage of annual detection of pulmonary tuberculosis and rifampicin-resistant Mycobacterium tuberculosis during the study years.

Result: Presumptive pulmonary tuberculosis patients with complete data (n = 3696) were included in the study. The overall prevalence of pulmonary tuberculosis was 11.7%, of which 8.1% were resistant to rifampicin. The study revealed that the incidence of pulmonary tuberculosis has been increasing, mainly in the recent four years. Likewise, an increase in rifampicin-resistant Mycobacterium tuberculosis was observed with considerable fluctuations. Age, human immunodeficiency virus infection, and presumptive rifampicin-resistant Mycobacterium tuberculosis infection were significantly associated with the presence of pulmonary tuberculosis. Moreover, pulmonary tuberculosis was more prevalent among participants in the productive-age group.

Conclusion: Although there have been fluctuations, an increasing of pulmonary tuberculosis and rifampicin-resistant Mycobacterium tuberculosis has been observed in recent years. Hence, prevention and treatment strategies for tuberculosis should be strengthened to alleviate the burden of pulmonary tuberculosis and rifampicin-resistant Mycobacterium tuberculosis in the study area.

背景:结核病(TB)是发展中国家主要的公共卫生问题。此外,耐多药结核病的出现也具有挑战性。然而,目前还没有关于研究地区肺结核和耐利福平结核分枝杆菌趋势的有组织数据:为了填补蒂格雷中部地区在 2018 年至 2023 年期间的信息空白,圣玛丽综合医院开展了一项回顾性横断面研究。使用标准核对表从 GeneXpert™ 结核病登记日志中收集数据,并使用社会科学统计软件包 22 版进行分析。在进行逻辑回归后,结果显示:P值为0:研究纳入了数据完整的推定肺结核患者(n = 3696)。肺结核的总发病率为 11.7%,其中 8.1%对利福平产生耐药性。研究显示,肺结核发病率一直在上升,主要是在最近四年。同样,耐利福平结核分枝杆菌的发病率也在上升,且波动较大。年龄、人体免疫缺陷病毒感染和推定的耐利福平结核分枝杆菌感染与肺结核的存在有显著相关性。此外,肺结核在生产年龄组的参与者中发病率更高:结论:近年来,肺结核和耐利福平结核分枝杆菌感染率虽有波动,但仍呈上升趋势。因此,应加强结核病的预防和治疗策略,以减轻研究地区肺结核和耐利福平结核分枝杆菌的负担。
{"title":"Trend of pulmonary tuberculosis and rifampicin-resistance among tuberculosis presumptive patients in Central Tigray, Ethiopia; 2018 -2023: a six-year retrospective study.","authors":"Guesh Gebremariam, Mulugeta Kiros, Selemun Hagos, Haftom Hadush, Amaha Gebremichael, Gebretsadkan Gebrekirstos, Aregawi Tesfay, Teumelsan Gebrewahid, Tesfay Berihu, Brhane Gebremariam","doi":"10.1186/s40794-024-00224-1","DOIUrl":"10.1186/s40794-024-00224-1","url":null,"abstract":"<p><strong>Background: </strong>Tuberculosis (TB) is a major public health concern in the developing countries. Moreover, the emergence of multidrug-resistant tuberculosis is challenging. However, there are no organized data on the trends of pulmonary tuberculosis and rifampicin-resistant Mycobacterium tuberculosis in the study area.</p><p><strong>Methods: </strong>A retrospective cross-sectional study was conducted to fill the information gap in Central Tigray at St. Mary General Hospital between 2018 and 2023. Data were collected from the GeneXpert™ tuberculosis registration logbooks using standard checklists and analyzed using Statistical Package for Social Science version 22. After performing logistic regression, a p-value < 0.05 with a corresponding 95% confidence interval was considered statistically significant. Moreover, chi square test for trend was performed to assess the percentage of annual detection of pulmonary tuberculosis and rifampicin-resistant Mycobacterium tuberculosis during the study years.</p><p><strong>Result: </strong>Presumptive pulmonary tuberculosis patients with complete data (n = 3696) were included in the study. The overall prevalence of pulmonary tuberculosis was 11.7%, of which 8.1% were resistant to rifampicin. The study revealed that the incidence of pulmonary tuberculosis has been increasing, mainly in the recent four years. Likewise, an increase in rifampicin-resistant Mycobacterium tuberculosis was observed with considerable fluctuations. Age, human immunodeficiency virus infection, and presumptive rifampicin-resistant Mycobacterium tuberculosis infection were significantly associated with the presence of pulmonary tuberculosis. Moreover, pulmonary tuberculosis was more prevalent among participants in the productive-age group.</p><p><strong>Conclusion: </strong>Although there have been fluctuations, an increasing of pulmonary tuberculosis and rifampicin-resistant Mycobacterium tuberculosis has been observed in recent years. Hence, prevention and treatment strategies for tuberculosis should be strengthened to alleviate the burden of pulmonary tuberculosis and rifampicin-resistant Mycobacterium tuberculosis in the study area.</p>","PeriodicalId":23303,"journal":{"name":"Tropical Diseases, Travel Medicine and Vaccines","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11215829/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141471005","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Exploring the utilization and perceptions of pre-travel health consultations in primary care settings in Saudi Arabia: a cross-sectional study. 探索沙特阿拉伯初级保健机构对旅行前健康咨询的利用和看法:一项横断面研究。
IF 3.1 Q2 Medicine Pub Date : 2024-06-15 DOI: 10.1186/s40794-024-00223-2
Naheel A AlAmer, Amani M AlQarni

Background: International travel exposes individuals to diverse health risks, necessitating proactive pre-travel health preparations. Saudi Arabia has witnessed increased outbound travel. This study addresses a critical gap in knowledge by investigating the utilization and perceptions of pre-travel health consultations among adults in the Eastern Province of Saudi Arabia.

Methods: This cross-sectional study surveyed patients at the Family and Community Medicine Center of Imam Abdulrahman Bin Faisal University during January 2024 to explore perceptions of pre-travel health consultations among the Saudi Arabian population. Adults aged 18 years or older in the waiting area were invited to complete a self-administered questionnaire.

Results: Of the 772 participants, 624 (80.8%) engaged in international travel within the last year. However, 593 (76.8%) had never sought pre-travel health consultations. Age, gender, and education level significantly influenced the pursuit of pre-travel health advice, with older individuals, females, and those with higher educational attainment more likely to seek consultations. Participants perceived vaccination recommendations (597, 77.4%) and disease prevention information (678, 87.8%) as crucial parts of pre-travel health consultations. However, barriers to seeking advice included perceived low risk (445, 74.8%), lack of awareness (215, 36.3%), time constraints (128, 21.6%), and cost concerns (92, 15.5%).

Conclusion: The low prevalence of pre-travel health consultations among travelers highlights the need for targeted educational campaigns and the integration of travel health services into primary healthcare. Addressing the identified barriers and leveraging preferred information sources are crucial steps towards enhancing the uptake of pre-travel health consultations, ultimately improving the health and safety of international travelers from the region.

背景:国际旅行使个人面临各种健康风险,因此需要积极做好旅行前的健康准备。沙特阿拉伯的出境游日益增多。本研究通过调查沙特阿拉伯东部省成年人对旅行前健康咨询的利用情况和看法,填补了这一重要的知识空白:这项横断面研究于 2024 年 1 月对伊玛目-阿卜杜勒拉赫曼-本-费萨尔大学家庭和社区医学中心的患者进行了调查,以了解沙特阿拉伯人对旅行前健康咨询的看法。候诊区内年满 18 岁的成年人受邀填写了一份自填问卷:在 772 名参与者中,有 624 人(80.8%)在过去一年中进行过国际旅行。然而,有 593 人(76.8%)从未进行过旅行前健康咨询。年龄、性别和教育程度对寻求旅行前健康咨询有很大影响,年龄较大者、女性和教育程度较高者更有可能寻求咨询。参与者认为疫苗接种建议(597 人,77.4%)和疾病预防信息(678 人,87.8%)是旅行前健康咨询的重要组成部分。然而,寻求建议的障碍包括认为风险低(445 人,占 74.8%)、缺乏认识(215 人,占 36.3%)、时间限制(128 人,占 21.6%)和费用问题(92 人,占 15.5%):旅行者进行旅行前健康咨询的比例较低,这突出表明有必要开展有针对性的教育活动,并将旅行健康服务纳入初级医疗保健中。消除已发现的障碍和利用首选信息来源是提高旅行前健康咨询普及率的关键步骤,最终将改善该地区国际旅行者的健康和安全。
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Tropical Diseases, Travel Medicine and Vaccines
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