Background While calls for institutionalization of evidence-informed policy-making (EIP) have become stronger in recent years, there is a paucity of methods that governments and organizational knowledge brokers can use to sustain and integrate EIP as part of mainstream health policy-making. The objective of this paper was to conduct a knowledge synthesis of the published and grey literatures to develop a theoretical framework with the key features of EIP institutionalization. Methods We applied a critical interpretive synthesis (CIS) that allowed for a systematic, yet iterative and dynamic analysis of heterogeneous bodies of literature to develop an explanatory framework for EIP institutionalization. We used a “compass” question to create a detailed search strategy and conducted electronic searches to identify papers based on their potential relevance to EIP institutionalization. Papers were screened and extracted independently and in duplicate. A constant comparative method was applied to develop a framework on EIP institutionalization. The CIS was triangulated with the findings of stakeholder dialogues that involved civil servants, policy-makers and researchers. Results We identified 3001 references, of which 88 papers met our eligibility criteria. This CIS resulted in a definition of EIP institutionalization as the “process and outcome of (re-)creating, maintaining and reinforcing norms, regulations, and standard practices that, based on collective meaning and values, actions as well as endowment of resources, allow evidence to become—over time—a legitimate and taken-for-granted part of health policy-making”. The resulting theoretical framework comprised six key domains of EIP institutionalization that capture both structure and agency: (1) governance; (2) standards and routinized processes; (3) partnership, collective action and support; (4) leadership and commitment; (5) resources; and (6) culture. Furthermore, EIP institutionalization is being achieved through five overlapping stages: (i) precipitating events; (ii) de-institutionalization; (iii) semi-institutionalization (comprising theorization and diffusion); (iv) (re)-institutionalization; and (v) renewed de-institutionalization processes. Conclusions This CIS advances the theoretical and conceptual discussions on EIP institutionalization, and provides new insights into an evidence-informed framework for initiating, strengthening and/or assessing efforts to institutionalize EIP.

Objetivo: analisar a temática do suicídio na perspectiva teórico-normativa dos direitos humanos dos pacientes. Metodologia: foi realizada pesquisa teórica e documental sobre os aspectos éticos e de direitos humanos dos pacientes em risco/tentativa de suicídio. Resultados: foram observadas violações aos direitos humanos dos pacientes em risco de saúde, nos serviços de saúde. Conclusão: é necessária a adoção de medidas para promover a alteração da situação de violação de tais direitos.

Introduction The Coronavirus Disease 2019 (COVID19) pandemic has struck Latin America and the Caribbean (LAC) particularly hard. One of the crucial areas in the international community’s response relates to accelerating research and knowledge sharing. The aim of this article is to map and characterise the existing empirical research related to COVID-19 in LAC countries and contribute to identify opportunities for strengthening future research. Methods In this scoping review, articles published between December 2019 and 11 November 2020 were selected if they included an empirical component (explicit scientific methods to collect and analyse primary data), LAC population was researched, and the research was about the COVID-19 pandemic, regardless of publication status or language. MEDLINE, EMBASE, LILACS, Scielo, CENTRAL and Epistemonikos were searched. All titles and abstracts, and full texts were screened by two independent reviewers. Data from included studies was extracted by one reviewer and checked by a second independent reviewer. Results 14,406 records were found. After removing duplicates, 5,458 titles and abstracts were screened, of which 2,323 full texts were revised to finally include 1,626 empirical studies. The largest portion of research came from people/population of Brazil (54.6%), Mexico (19.1%), Colombia (11.2%), Argentina (10.4%), Peru (10.3%) and Chile (10%), while Caribbean countries concentrated 15.3%. The methodologies most used were cross-sectional studies (34.7%), simulation models (17.5%) and randomized controlled trials (RCTs) (13.6%). Using a modified version of WHO’s COVID-19 Coordinated Global Research Roadmap classification, 54.2% were epidemiological studies, followed by clinical management (22.3%) and candidate therapeutics (12.2%). Government and public funds support were reported in 19.2% of studies, followed by universities or research centres (9%), but 47.5% did not include any funding statement. Conclusion During the first part of the COVID-19 pandemic, LAC countries have contributed to the global research effort primarily with epidemiological studies, with little participation on vaccines research, meaning that this type of knowledge would be imported from elsewhere. Research agendas could be further coordinated aiming to enhance shared self-sufficiency regarding knowledge needs in the region.

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The quantity and complexity of scientific and technological information provided to policymakers have been on the rise for decades. Yet little is known about how to provide science advice to legislatures, even though scientific information is widely acknowledged as valuable for decision-making in many policy domains. We asked academics, science advisers, and policymakers from both developed and developing nations to identify, review and refine, and then rank the most pressing research questions on legislative science advice (LSA). Experts generally agree that the state of evidence is poor, especially regarding developing and lower-middle income countries. Many fundamental questions about science advice processes remain unanswered and are of great interest: whether legislative use of scientific evidence improves the implementation and outcome of social programs and policies; under what conditions legislators and staff seek out scientific information or use what is presented to them; and how different communication channels affect informational trust and use. Environment and health are the highest priority policy domains for the field. The contextspecific nature of many of the submitted questions-whether to policy issues, institutions, or locations-suggests one of the significant challenges is aggregating generalizable evidence on LSA practices. Understanding these research needs represents a first step in advancing a global agenda for LSA research.Notes 1 By policymakers, we mean those in government who use science to make policy decisions, whether members of staff or elected representatives. ARTICLE PALGRAVE COMMUNICATIONS | https://doi.

A Revista Lancet Countdown: Acompanhando o Progresso em Saúde e Mudanças Climáticas é uma colaboração internacional multidisciplinar que objetiva monitorar as relações entre saúde pública e mudanças climáticas. Reúne 35 instituições acadêmicas e agências das Nações Unidas de todos os continentes, embasando-se na expertise de climatologistas, engenheiros, economistas, cientistas políticos, profissionais de saúde pública e médicos. Todos os anos, a Lancet Countdown publica uma avaliação anual do estado das mudanças climáticas e da saúde humana, procurando oferecer aos tomadores de decisão acesso a orientações para uma política baseada em evidência de alta qualidade.

Background Evidence briefs for policy (EBP) draw on best-available data and research evidence (e.g., systematic reviews) to help clarify policy problems, frame options for addressing them, and identify implementation considerations for policymakers in a given context. An increasing number of governments, non-governmental organizations and research groups have been developing EBP on a wide variety of topics. However, the reporting characteristics of EBP vary across organizations due to a lack of internationally accepted standard reporting guidelines. This project aims to develop a STandard reporting guideline of Evidence briefs for Policy (STEP), which will encompass a reporting checklist and a STEP statement and a user manual. Methods We will refer to and adapt the methods recommended by the EQUATOR (Enhancing the QUAlity and Transparency Of health Research) network. The key actions include: (1) developing a protocol; (2) establishing an international multidisciplinary STEP working group (consisting of a Coordination Team and a Delphi Panel); (3) generating an initial draft of the potential items for the STEP reporting checklist through a comprehensive review of EBP-related literature and documents; (4) conducting a modified Delphi process to select and refine the reporting checklist; (5) using the STEP to evaluate published policy briefs in different countries; (6) finalizing the checklist; (7) developing the STEP statement and the user manual (8) translating the STEP into different languages; and (9) testing the reliability through real world use. Discussion Our protocol describes the development process for STEP. It will directly address what and how information should be reported in EBP and contribute to improving their quality. The decision-makers, researchers, journal editors, evaluators, and other stakeholders who support evidence-informed policymaking through the use of mechanisms like EBP will benefit from the STEP. Registration We registered the protocol on the EQUATOR network. (https://www.equator-network.org/library/reporting-guidelines-under-development/#84)

Resumo O suicídio é um grave problema de saúde pública mundial. Este estudo parte de um referencial teórico-normativo fundamentado nas normas de direitos humanos aplicáveis aos pacientes, no contexto dos cuidados em saúde. Objetivou-se investigar a violação dos direitos humanos dos pacientes em risco de suicídio. Foram realizadas 11 entrevistas semiestruturadas com profissionais da saúde, pacientes e familiares em quatro capitais brasileiras. Trata-se de uma pesquisa empírica qualitativa apoiada no método hermenêutico-dialético. Foi identificada a dificuldade dos profissionais em lidar com a temática, especialmente através da reprodução de condutas estigmatizantes, morais, religiosas, paternalistas e/ou hipervigilantes. Observou-se a violação dos direitos humanos dos pacientes, comprometendo o cuidado ofertado, a continuidade do tratamento, o protagonismo, a privacidade e a capacidade decisional do paciente, além do aumento da vulnerabilidade e do risco de novas tentativas. Entre os entrevistados, não houve consenso a respeito da conscientização das violações por parte dos profissionais. A proteção desses pacientes pressupõe a adoção de medidas de capacitação das equipes de saúde, processos de sensibilização e de informação para a sociedade, assim como a criação de políticas e legislações específicas, de modo a ampliar o entendimento sobre direitos humanos e prevenção do suicídio.