Addressing social determinants of noncommunicable diseases in primary care: a systematic review

Abstract Objective To explore how primary care organizations assess and subsequently act upon the social determinants of noncommunicable diseases in their local populations. Methods For this systematic review we searched the online databases of PubMed®, MEDLINE®, Embase® and the Health Management Information Consortium from inception to 28 June 2019, along with hand-searching of references. Studies of any design that examined a primary care organization assessing social determinants of noncommunicable diseases were included. For quality assessment we used Cochrane’s tool for assessing risk of bias in non-randomized studies of interventions. We used narrative data synthesis to appraise the extent to which the assessments gathered data on the domains of the World Health Organization social determinants of health framework. Findings We identified 666 studies of which 17 were included in the review. All studies used descriptive study designs. Clinic-based and household surveys and interviews were more commonly used to assess local social determinants than population-level data. We found no examples of organizations that assessed sociopolitical drivers of noncommunicable diseases; all focused on sociodemographic factors or circumstances of daily living. Nevertheless, the resulting actions to address social determinants ranged from individual-level interventions to population-wide measures and introducing representation of primary care organizations on system-level policy and planning committees. Conclusion Our findings may help policy-makers to consider suitable approaches for assessing and addressing social determinants of health in their domestic context. More rigorous observational and experimental evidence is needed to ascertain whether measuring social determinants leads to interventions which mitigate unmet social needs and reduce health disparities.


Introduction
Primary health care is a whole-of-society approach to health that depends on integrated primary care and essential public health functions; empowered people and communities; and multisectoral policy and action. 1 World Health Organization (WHO) Member States have unanimously committed to use primary health care as the main vehicle for attaining universal health coverage. [1][2][3][4] Given that health services are thought to be responsible for only a fifth of health outcomes, 5,6 primary care systems are increasingly being reoriented to proactively assess and address local social determinants of health, [7][8][9][10][11][12] particularly the social determinants of noncommunicable diseases. These diseases are responsible for over 70% of global mortality (41 million out of 58 million annual deaths). 13,14 Socioeconomic factors are associated with exposure to behavioural risk factors for and mortality from noncommunicable diseases, 15,16 and exposure to noncommunicable disease risk factors, such as poverty, tobacco or unhealthy foods, occurs at the local levels where people live and work. Primary care organizations therefore have a strategic role to play in prevention and control of noncommunicable diseases. This role was emphasized in WHO's Commission on the Social Determinants of Health 2007 report, Challenging inequity through health systems. 17 Reforming primary care to engage with public health func-tions in collaboration with community stakeholders is also a way of enacting the commitments made in the Declaration of Astana on revitalizing primary health care in the 21st century. 12 Social determinants, which have been defined as "the conditions in which people are born, grow, work, live and age, and the wider set of forces and systems shaping the conditions of daily life," 18 account for approximately half of all variation in health outcomes. 6,[19][20][21][22] The WHO Commission on the Social Determinants of Health urged Member States to "go beyond contemporary concentration on the immediate causes of disease" to focus on these "causes of the causes. " 17 The Commission's conceptual framework has three elements covering different domains. 23 First are the sociopolitical factors that influence distributions of health outcomes across populations (such as social and economic policy, cultural norms and societal values). These factors can be distinguished from the sociodemographic factors according to which health is unequally distributed (such as income, education, gender and ethnicity or race) and the circumstances of daily life which more directly influence people's exposure and vulnerability to adverse health outcomes (such as age, housing and food security, sanitation, health behaviours and access to health care). The Commission's framework for action on the social determinants of health conceptually differentiates policy interventions in terms of their target population: individuals (microlevel), communities (mesolevel) and whole of society (macrolevel). 23 Countries as diverse as Azerbaijan, Ethiopia and the United Kingdom of Great Britain and Northern Ireland are currently reforming their primary care systems to address the social determinants of noncommunicable diseases. Yet it remains unclear how primary care organizations can most effectively collect person-and population-level data to subsequently act upon identified needs. 7,12,24 Much of the existing research on assessing social determinants of health has focused on secondary care settings in high-income countries. [24][25][26][27] To address this gap, we systematically reviewed the literature to collate examples of primary care organizations that had performed assessments of the social determinants of noncommunicable diseases with the intention of subsequently acting upon the knowledge generated. We aimed to determine which social determinants of health are most commonly assessed, the approaches used to collect data, what actions resulted and what barriers and enablers were reported. A secondary aim was to examine whether routine assessments of the social determinants of health were more likely to report actions than were non-routine, or "one-off " assessments.

Methods
Our systematic review followed Cochrane guidance 28 and was reported in accordance with the 2009 Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. 29 The protocol was registered with the PROSPERO prospective register of systematic reviews in July 2019 (CRD42019141291).

Search strategy
We searched the online databases of MEDLINE ® , Embase ® , PubMed ® and the Health Management Information Consortium on 28 June 2019 without restrictions on language, period or country (the full search strategy is available in the data repository). 30 We also manually searched the reference lists of included studies and contacted key authors and policy experts at WHO to find any additional studies.
We included all study designs that examined one or more historic or contemporary primary care organization committing resources to assessing the social determinants of noncommunicable diseases in their local community with the intention of subsequently intervening. Studies that described the assessment activities of specific primary care staff cadres, such as community health workers, were also included.
We excluded papers such as editorials and reviews that did not present primary data, but we hand-searched their reference lists and included any eligible original studies. As our focus was real-world practice, we excluded papers that only described theoretical models or unrealized organizational plans. We excluded papers that described single-issue initiatives for narrow subpopulations if these were not based on community-wide assessments. We excluded studies that focused exclusively on paediatric populations, unless the primary care organization was a community-based paediatric service, so that their entire patient population was included. We also excluded studies that did not report the intention of assessing impact on services or health outcomes.
Two researchers independently screened all titles and abstracts and then the full texts. Cohen's kappa coefficient (κ) and percentage agreement were calculated for both stages of screening. 31 Disagreement was resolved by discussion and arbitration by a third researcher if necessary.

Data extraction, synthesis and analysis
Two researchers independently extracted the data using a form developed from the Cochrane template, 32 including study design, setting, assessment approach, factors identified by the assessment and subsequent community-level actions. We used narrative data synthesis to appraise whether the health assessments in the included studies gathered data on the domains of the WHO social determinants of health framework. 23 We used also used Geoffrey Roses's population versus high risk conceptual approach to assess whether different organizations assessed and addressed social determinants of health at the individual and/or community levels. 33 Given the lack of formal consensus around the precise boundaries of the social determinants of health, 34,35 we included all data that the authors self-identified as social determinants, including individual-level sociodemographic characteristics.

Risk of bias assessment
Two reviewers independently assessed the risk of bias of each included study using Cochrane's risk of bias tool for non-randomized studies of interventions. 36 Guided by the Cochrane handbook, 28 we rated studies as having low, moderate, serious or critical risk of bias across seven domains and overall.

Search results
Our searches identified 666 records of which 17 studies from 15 different primary care organizations met the inclusion criteria after two stages of screening (Fig. 1). Cohen's κ was > 0.80 and agreement was > 95% at every stage of screening.

Study characteristics
The characteristics of the included studies are summarized in Table 1. All studies took place in high-or middle-income countries, with nine studies conducted in the United States of America (USA), [37][38][39][40][41]43,47,48,50 three in South Africa, 42,46,49 three in Canada [51][52][53] and two in the United Kingdom (one in England 45 and one in Wales 44 ).
Six of the 17 records were published after 2014 while the oldest records came from the second volume of the 1984 Institute of Medicine report on community-oriented primary care. This volume described case studies of USA primary care organizations, five of which met our inclusion criteria. [37][38][39][40][41] One record presented findings from a community-oriented primary care project in South Africa in the 1940s. 42 Among the remaining papers, a further seven were descriptive case studies, 42,43,[46][47][48]51,53 making this the most prevalent study design. There was one retrospective cohort study, 52 two rapid participatory appraisals, 45,49 a mixed-methods pilot study 50 and a cross-sectional study that also provided a narrative account of efforts to address social determinants. 44 Three papers reported on the same Canadian primary care organization. [51][52][53] Ten of the 17 studies described efforts led by primary health-care clinicians who had been actively involved in new initiatives to gather data on the social determinants of health in their local communities. [43][44][45][46][47][48][50][51][52][53] Most papers aimed to describe novel assessment initiatives. For three papers these initiatives were nested within evaluations of broader interventions. [37][38][39][40][41]46,49 Systematic reviews Primary care and social determinants of noncommunicable diseases Luke N Allen et al.

Assessment activities reported
The included studies examined a wide range of domains of the social determinants of health, 20 of which were captured by two or more studies (Table 2; available at: http:// www .who .int/ bulletin/ volumes/ 98/ 11/ 19 -248278). Circumstances of daily life and indicators of socioeconomic position were the most commonly assessed. No studies assessed social cohesion. Assessed in 11 studies (9 organizations), the most common indicators of socioeconomic position were measures of income or financial situation. Additional population stratification factors, such as race and ethnicity, nationality, religion, disability, sexual orientation and language were only assessed in two recent studies.
Only two studies (reporting on the same primary care organization) explicitly sought to assess both sex and gender identity. 51,53 Two studies did not report which specific social determinants of health data they were assessing. 46,49 No studies assessed any of the wider sociopolitical factors.

Approach to data collection
Ten studies described routine data collection activities on the social determinants of health, 37,39,40,42,46,48,49,[51][52][53] six described non-routine or one-off assessments, 41,[43][44][45]47,50 and one study was unclear. 38 Almost all organizations that employed routine assessments collected individual-level data from patients or their proxies, often within clinic receptions or waiting areas (Table 3). One study additionally linked individual records to neighbourhood median household income level 52 and another study supplemented patient-level data with routine household surveys conducted by community health workers. 49 Greater heterogeneity in data domains and collation methods was observed among studies describing non-routine social determinants of health assessments. Aggregate-level administrative data on social determinants of health were collated for the primary care organization's catchment areas (such as neighbourhood deprivation) or such data were linked to patient rosters using identifiers such as postcode, 44,45,47 household surveys, 40,41,46 in-clinic surveys 50 and telephone interviews. 43 In total, six studies involved the collection of population-level data. 37,39,42,44,47,52 Publicly-available data sources included censuses, state health departments and nongovernmental organizations. Non-publicly accessible sources (those requesting special data requests) included local, regional and federal government departments for health, social services, labour and education, municipal police departments, regional health-planning agencies and certain national data sets.

Actions reported
In addition to action to extend data collection to other primary care sites, 50,51 the studies described several other initiatives by primary care organizations to address the social determinants of health (Table 3; Box 1). These initiatives ranged from individual-focused biomedical interventions through to population-level, health-in-all-policy partnerships with local authorities and non-health agencies. Building on the WHO conceptual framework for action on the social determinants of health, we present a new conceptual taxonomy of the different strata addressed by the studied primary care organizations ( Fig. 2), dividing actions into macro, meso and micro levels.
We identified several factors as potential facilitators to effective collection, analysis and translation of social determinants of health data into action. At organizational and system levels, facilitating included strong commitment in terms of leadership, funding and human resources, and having health equity embedded within the organization's strategic plans. 44,53 Pre-existing collaborative multisectoral partnerships were also believed to enable multifaceted responses to community health needs identified by social determinant assessments. 47 Electronic data collection using tablet computers and mobile phones was believed to be feasible and acceptable within both well-and under-resourced clinical settings. 49,51 Translating surveys into multiple languages was believed to improve response rates and overall data quality. [51][52][53] Having social determinants of health data entry fields integrated • 64 articles did not assess social determinants of health • 37 articles were inaccessible for the authors • 18 articles did not present primary data • 9 were theoretical or protocol papers • 6 articles did not assess noncommunicable diseases • 6 articles focused on a subpopulation • 4 articles did not report impact • 1 article was an evaluation of a biomedical intervention • 1 article not conducted in a primary care setting 503 records excluded within electronic health records was believed to improve the documentation of unmet social needs and communication of such information across care teams. 48 Missing data limited the completeness of the primary data collected for more sensitive sociodemographic information such as income. Data representativeness was potentially limited where only a sub-sample of key informants provided social determinants of health information on behalf of the wider community. 43,51,52 Given that populationlevel data sets were often sourced from multiple organizations, the quality and compatibility of linked data were hindered by variations in data collection time periods, different geographical boundaries and varying coverage of the population. 40,44 Linking population-level data to individual-level data was difficult in practices using hard-copy medical records. 39 The time and human resource investments required for data collection, processing, analysis and reporting was raised as a key challenge for implementing social determinants of health data collection, even in wellresourced primary care settings. 43,44,48,49 Finally, public trust in the people and Table 3. Source of individual-and population-level data and types of actions by primary care organizations involved in assessing and addressing the social determinants of health

Risk of bias assessment
The overall risk of bias was serious for 15 studies and critical for two studies. Due to the reliance on descriptive study designs, most studies provided limited detail regarding who received the social determinants of health assessment intervention and how these interventions were implemented. Another important source of potential bias was in the at-tribution of actions (that were not prespecified) to the social determinants of health assessment intervention without comparison to a control group or accounting for other potentially confounding factors. Domain-specific risk of bias assessments are presented in the data repository. 30

Discussion
Our review provides primary healthcare practitioners and policy-makers with an overview of the approaches taken to assess and address social deter-minants of noncommunicable diseases by 15 primary care organizations. Although this policy objective is a leading priority for international health systems, we found very few contemporary examples in the peer-reviewed literature that met the inclusion criteria for this study. There was marked heterogeneity in the domains assessed by the different organizations, and no assessments of macro-level sociopolitical factors that influence distributions of health across populations. Organizations tended to collect individual-level data in clinical settings rather than population-level

Individual-focused interventions
Several study sites identified patients with unmet social needs and provided these individuals with educational materials, 43 referred them on to relevant services 48,49 or connected them with community workers. 42,50 New services for specific subgroups Four study sites identified specific subpopulations with high levels of need: people of Asian ancestry, 45 older adults, 39,43 and Cambodian refugees. 40 New services were created for these groups including: tailored educational materials, health services, and social interventions such as working with landlords to improve rental housing stock; 40 lobbying for improved transport infrastructure; 39 and setting up community welfare groups. 45

Mesolevel actions: targeting communities New clinical services that benefit the entire community
Five study sites developed new clinical services that stood to benefit the entire community: relocating pre-existing clinical services and starting a mobile outreach clinic; 47 launching a health bus and a new practice-based health promotion programme at the local produce market; 45 extending the scope of clinical services offered by the primary health-care practice; 44 hiring new community health workers; 50 and an array of new clinical services offered by ward-based outreach teams. 49

New integrated health and social services
The academic primary health-care practice network in Alachua county, USA, described the creation of a new integrated health and social care community resource centre. 47 Another study of outreach teams in seven provinces in South Africa described the initiation of multidisciplinary meetings to plan integrated services with local populations. 49

New non-clinical services
After finding that access to local health services was poor, the neighbourhood health centre in Boston in the USA, sought funding for new transport infrastructure. The centre also applied for funding to improve the local housing stock and sought to influence television broadcasting to promote anti-violence messages in response to high homicide rates uncovered by their data. 39 The Bronx community health centre in New York, USA, worked with landlords to improve housing standards and remove lead-based paint causing respiratory problems identified by their linkage of health and social determinants of health data. 40 In the study in Hyndburn, England, the primary health-care partnership instigated the establishment of a credit union after finding that debt and low income was a problem for many local residents. 45 The Pholela project workers in KwaZulu-Natal, South Africa, built new vegetable gardens to help improve the local population's nutritional status. 42 South Africa's ward-based outreach teams in seven provinces also set up several garden projects, as well as helping communities obtain new toilets, water banks, food parcels, child support grants and overarching birth certification. 49

Macrolevel actions: targeting public policies Lobbying and introduction of new legislation and policies
The health-centre partnership in Albuquerque, USA, went beyond delivering new programmes and services to successfully lobby for new legislation (the Community Health Workers Act). 50 Due in part to a previous initiative, 51 regional authorities directed all hospitals within central Toronto city, Canada, to begin standardized sociodemographic data collection. The health centre in Boston in the USA modified existing parent counselling protocols to de-emphasize practices that were believed to "condone or may predispose children to violence" in an effort to prevent future violence. 39 As a result of presenting health disparity hot-spot maps (displaying the location and intensity of socioeconomic issues) in Alachua county, USA, community organizing and advocacy activities were initiated to lobby for better social conditions. 47

New representation in policy and planning processes
Assessing local needs is believed to have strengthened relationships across the primary health-care partnership in Hyndburn, England -primarily between the general practitioner's surgery and the local government. 45 The results of the assessment contributed to environmental policy-making and decisions around housing developments and local town regeneration. In South Africa, ward-based outreach teams and their primary care managers established partnerships with local government, nongovernmental organizations, faith organizations, private sector agencies, and local village councils, allowing them to collaboratively develop new services and have a voice in local decision-making. 49 Finally, as a result of developing a multi-agency data set on health and social inequality in the study in Caerphilly, Wales, representatives from local general medical practices became major partners with local authorities and local communities, contributing to planning processes and participating in development of future community strategies. 44 Systematic reviews Primary care and social determinants of noncommunicable diseases Luke N Allen et al.
data. There was a broad range of actions targeting individuals, communities and the whole of society. The use of descriptive case studies and an absence of longterm evaluations of health outcomes among the included studies limits the conclusions we can reach about the relative merits of each approach. Nevertheless, the heterogenous approaches described in this paper highlight diverse options for care providers and policymakers to consider. Gold-standard approaches to collection of data on the social determinants of health in health-care settings have yet to be identified. Nevertheless, the WHO Commission's framework 23 provides a useful starting point for primary care organizations in defining, which specific factors are most relevant to their local context. As observed in our review, the specific domains of the social determinants of health assessed and the methods for data collection will likely vary according to an organization's purpose for assessment and the resources available to support data collection, analysis and response.
Approximately half of the studies in our review assessed the social determinants of health via individual-level surveys in clinical settings. These data can complement existing biomedical information from medical records. A 2018 scoping review found that a growing number of screening tools are being used around the world to help frontline clinicians collect data on social determinants. 54 These data are mainly being used in a case-finding capacity to identify individuals with multiple domains of social risk. 55 The combination of individual-level social data (such as on poverty, housing and food insecurity) and clinical health data (such as blood pressure, cholesterol levels, medications and pre-existing conditions) can help health workers to identify population groups with specific needs and inform the design of appropriate interventions. However, approaches that rely on data collected solely in clinic settings will exclude vulnerable members of the local community who are not registered or do not seek care from primary care providers. 56,57 This approach may also fail to capture higher-order and populationwide factors such as welfare policy, transport networks and sanitation.
The other half of the reviewed studies either collected new population-level data or collated pre-existing population-level sociodemographic data sets. These data collection activities were often stand-alone endeavours as opposed to routine, systematized activities. Aggregated community-level data can conceal within-population inequalities, but otherwise tend to provide a more representative picture than extrapolating from patient registries. Whether data are at the individual or population level, it is paramount that primary care organizations carefully consider the representativeness of their data sources. 58,59 The actions of the primary care teams in South Africa 49 and the United Kingdom 44,45 model the primary healthcare philosophy of integrating public health and primary care functions to engage in intersectoral action. 60 Nevertheless, we did not find any examples of primary health-care organizations that employed routine systems for collating population-level data on the social determinants of health and that worked collaboratively on an everyday basis. Intersectoral collaboration was highlighted as an enabler of population-level social determinants of health assessment. Yet the reviewed studies suggest that there are challenges to finding the human, financial and technological re-

Systematic reviews
Primary care and social determinants of noncommunicable diseases Luke N Allen et al. sources required to build and maintain routine population-level assessment systems on the social determinants of health. These roles can be provided by organizations responsible for planning and resourcing local health and social services (such as health ministries), academic institutions, or those representing primary care professionals (such as professional associations and governing bodies). Contemporary examples include population health data parsed for primary care organizations by Public Health England, 61 the American Board of Family Medicine and University of Missouri, 62 and the Slovenian National Institute of Public Health. 63 There are numerous other systems containing population-level data on a wide range of social determinants of health indicators that are not currently linked to specific primary care practice populations. 64 Further research should explore how to support the use of these data in primary care to plan local population services that are responsive to community needs.
Assessing the domain of wider sociopolitical factors was another identified gap in data collection by primary care organizations. This omission may be justified given that the purpose of collecting data on the social determinants of health tended to focus on the local community. However, the gap may also stem from a lack of clarity on which measures within this domain are relevant, feasibly measured and actionable for primary care organizations. Understanding how to collect data on wider sociopolitical factors represents an important area for future research. Further gaps include information around funding mechanisms, workforce arrangements and the interface with public health agencies.
Almost all the primary care organizations used new knowledge on local social determinants of health to design and deliver novel interventions with the goal of reducing health inequalities and improving population health outcomes. These ranged from downstream individual-focused activities like producing educational materials, to upstream health-in-all-policies approaches, such as joining local authority planning and commissioning boards. Similar themes of action are reflected in the 2019 consensus report on the integration of health and social care in the USA. 24 Our social determinants of health taxonomy of actions builds on previous research 22 and the WHO Commission's report 65 to provide a way of thinking through the various levels where primary care organizations can act to make positive changes.
An important consideration for future research is how, when and where primary care organizations should engage with traditional public health activities. Our review has illustrated the heterogeneity in primary care activities on addressing the social determinants of health. However, despite decades of work to define the characteristics of primary care, 66 there is no consensus in the health policy community around exactly which activities and functions primary care ought to perform. One approach is unlikely to be suitable for all settings, as different primary care systems have different skills, resources, and cultural expectations. There are already marked contrasts between even closely related systems. While Dutch family physicians recently rejected mooted new public health responsibilities 67 almost all general practitioner surgeries in England 68 have taken on responsibilities for addressing neighbourhood inequalities and improving population health. 69 Our review has several strengths. It was conducted in line with Cochrane and PRISMA guidelines and used a robust search strategy with independent dual review with good agreement at every stage. The review addresses an important evidence gap for global primary health care and provides detailed and pragmatic insights for clinicians and policy-makers. Limitations of this review primarily relate to the types of studies included. Most were case studies detailing implementation approaches rather than quantifying associations between social determinants of health assessment and subsequent actions and outcomes. In particular, the absence of health outcomes data reported in the included studies highlights the challenges primary care organizations face with finding the resources to evaluate downstream outcomes of interventions that may take several years to manifest. This aligns with public health research more broadly 70,71 and social determinants of health-oriented primary care research specifically, where the field is hampered by a lack of randomized controlled trials and of methodological tools for evaluating complex interventions. 72 To examine whether assessment of the social determinants of health leads to interventions mitigating unmet social needs and health disparities, future research should endeavour to use longer follow-up periods and more rigorous observational and experimental methods. 73,74 Despite stating an intention to use social determinants of health data collection to inform action, six of the 17 studies did not report on any actions. We did not find any studies from low-income countries that met the inclusion criteria and our review may also have missed unpublished international examples, thus limiting the generalizability of our findings. Despite these limitations, case studies arguably provide useful evidence for how and why a particular approach was employed.

Conclusions
Tasked with the mandate of the Declaration of Astana and facing a rising burden of noncommunicable diseases, policymakers are reorienting their primary care systems to proactively address the social determinants of noncommunicable diseases. We have identified several promising primary care approaches for measuring and mobilizing action on social determinants of noncommunicable diseases. The evidence presented could assist care providers and policy-makers in considering which domains of social determinants of health to measure, which methods to use for collecting and collating this data, and how and at what level primary care organizations are positioned to intervene on local social determinants of health. Future research should examine undocumented innovators in this field and aspire to more rigorous observational and experimental study designs examining the impact of social determinants of health assessment on interventions to address local social determinants of health and health disparities. ■

Resumen
Abordar los determinantes sociales de las enfermedades no transmisibles en la atención primaria: una revisión sistemática Objetivo Estudiar cómo las organizaciones de atención primaria evalúan y aplican posteriormente los determinantes sociales de las enfermedades no transmisibles en sus poblaciones locales. Métodos Para esta revisión sistemática se realizaron búsquedas en las bases de datos en línea de PubMed®, MEDLINE®, Embase® y el Health Management Information Consortium desde su inicio hasta el 28 de junio de 2019, junto con una búsqueda manual de referencias. Se incluyeron estudios de todos los diseños que analizaron a una organización de atención primaria en la que se evaluaban los determinantes sociales de las enfermedades no transmisibles. Para la evaluación de la calidad se utilizó la herramienta de Cochrane para evaluar el riesgo de sesgo en los estudios no aleatorizados de las intervenciones. Se utilizó la síntesis narrativa de datos para evaluar el alcance de las evaluaciones para recopilar datos sobre los dominios del marco de los determinantes sociales de la salud de la Organización Mundial de la Salud. Resultados Se identificaron 666 estudios, de los cuales 17 se incluyeron en la revisión. Todos los estudios utilizaron diseños de estudio descriptivos. Se utilizaron las encuestas y las entrevistas en los consultorios y en los hogares con mayor frecuencia que los datos a nivel de la población para evaluar los determinantes sociales locales. No se encontraron ejemplos de organizaciones que evaluaran los factores sociopolíticos determinantes de las enfermedades no transmisibles, ya que todas se centraban en los factores sociodemográficos o en las circunstancias de la vida cotidiana. No obstante, las medidas que se adoptaron para abordar los determinantes sociales fueron desde intervenciones a nivel individual hasta medidas a nivel de la población y la integración de la representación de las organizaciones de atención primaria en los comités de planificación y de políticas a nivel del sistema. Conclusión Los resultados obtenidos pueden ayudar a los responsables de formular las políticas a considerar los enfoques adecuados para evaluar y abordar los determinantes sociales de la salud en su contexto nacional. Se necesitan evidencias observacionales y experimentales más rigurosas para determinar si la medición de los determinantes sociales conduce a las intervenciones que mitigan las necesidades sociales que no se atienden y que reducen las desigualdades en la salud.

Systematic reviews
Primary care and social determinants of noncommunicable diseases Luke N Allen et al.