Abstract
Objectives
Poor social conditions are strong determinants of poor health but positive health and healthcare changes caused by social interventions are difficult to demonstrate. In 2006, in Trieste (Italy), a social intervention known as ‘Habitat Microaree’ (HM) project was implemented in eight deprived neighbourhoods. In 2016, an observational study was launched to assess the impact of the HM project on healthcare.
Design
Retrospective cohort study.
Setting
The eight geographically defined neighbourhoods of Trieste involved in the 2006 HM project, accounting for a total of 11 380 residents.
Participants
Participants were all residents in the intervention areas. By means of a propensity score based on deprivation index, age, sex, Charlson index and drug utilisation, a non-participating, comparison group was defined.
Intervention
The community-based intervention consisted of facilitating access to social services and outpatient healthcare facilities, coordinating intersectoral public services and specifically planning hospital discharge. These services were not provided in other areas of the city.
Outcome measures
Hospital admissions and emergency department access.
Results
We followed 16 256 subjects between 2008 and 2015. Living in microareas was associated with an HR for first hospital admission, for all causes, of 0.95 (95% CI 0.91 to 0.99); while the HR for urgent admissions in females was 0.92 (95% CI 0.85 to 1.00). The HR for psychiatric disorders, in females, was 0.39 (95%CI 0.18 to 0.82); in particular, the HR for psychosis was 0.15 (95% CI 0.05 to 0.51). The HR for acute respiratory diseases in females was 0.44 (95% CI 0.21 to 0.95). In males, the HR for genitourinary diseases and heart diseases were 0.65 (95% CI 0.42 to 1.01) and 0.72 (95% CI 0.54 to 0.97), respectively. Concerning urgent multiple admissions, the OR for fractures in females was 0.75 (95% CI 0.58 to 0.97).
Conclusion
In the study period, the effects on healthcare appear evident, especially in females.
Keywords: public health, epidemiology, social medicine
Strengths and limitations of this study.
This study involved a large cohort for a long follow-period and the use of administrative databases as a data source, provided a complete picture of the subjects’ access to healthcare facilities, diagnoses, therapies and treatments in the study period.
To our knowledge, this is one of few studies that evaluate the effectiveness of a social intervention in terms of impact on health service.
Our data derive from the administrative databases through an anonymous identifier, therefore, although not all residents were directly involved in the Habitat Microaree (HM) project, in our analysis all residents in the selected microareas were considered as participants in the HM project.
Between 2009 and 2012, the HM project was extended to a further three microareas. Therefore, a number of residents, initially considered as non-participants, were subsequently involved in the intervention.
Our results suggest that the HM project was more effective among females. This represents a limitation to the generalisability of the results.
Introduction
Material deprivation is an outcome-based measure of material well-being and material deprivation rate is an indicator in the European Union statistics on income, and living conditions, adopted by the Social Protection Committee and used by the European Commission to set targets for the Member States.1 2 Townsend considered the material deprivation as the ‘inability of living a decent life’.3 He stated ‘People can be said to be deprived if they lack the types of diet, clothing, housing, environmental, educational, working and social conditions, activities and facilities which are customary, or at least widely encouraged or approved, in the societies to which they belong. They fall below standards of living which either can be shown to be widespread in fact or are socially accepted or institutionalised’.4 Sen agreed with Townsend on the concepts of ‘shame’ and ‘inability to live a decent life with dignity’ to explain the concept of material deprivation.5 To date, authors converge towards a definition of material deprivation as ‘exclusion from the minimum acceptable way of life in one’s own society because of inadequate resources’6–11 or ‘the lack of socially perceived necessities’.7 12 Indeed, there is mounting evidence of an association between material deprivation and poor health conditions, in particularly with regard to chronic diseases whose risk increases over the life course.13 A Spanish nationwide small area study aimed to investigate the excess of mortality by first 10 leading causes associated to deprivation indexes, found that the higher the deprivation levels the higher the mortality risks, although this relation varied by gender and region. According to the authors, these findings support the idea that material deprivation causes health inequality through two mechanisms: by increasing the general susceptibility to diseases that lead to an excess of mortality for a wide range of causes; and through a set of more specific factors that lead to an excess of mortality for gender-specific causes.14 15
Furthermore, it has been shown that there is an increasing trend in annual access to emergency and urgent care in developed countries.16 Studies from the USA, Canada, the UK and Australia consistently reported demand for emergency department (ED) care increased from 3% to 6% per year. Between 1996 and 2006, in the USA, accesses to ED rose from 34.1% to 40.5% while in UK demand has more than doubled from 6.8 million ED accesses in 1966 to 14.3 million in 2012.17–20 However, according to the available studies, this phenomenon is attributable mainly to people with primary care problems who make improper use of emergency and urgent care services to access care. Relevant proportions of patients, ranging from 10% to 60%, could be managed using services with lower and more appropriate care, and more accessible primary care could reduce unplanned secondary care use.16 21 Material deprivation is one of the factors that affect the way health services are used; in a population-based cohort study, Brokamp et al22 found that a 10% increase in deprivation level caused a 1.03-fold increase (95% CI 1.03 to 1.04) in length of hospital stay and a 1.02-fold increase (95% CI 1.01 to 1.04) in risk of hospital utilisation. Raphael23 gave the definition of social determinants of health as ‘economic and social conditions that shape the health of individuals, communities and jurisdictions as a whole’. Gender, education, income, housing, employment and access to healthcare shown an association with ill health.
Strong associations between social determinants and several health outcomes in different populations have been well documented as reported in Braveman and Gottlieb.24 Collaboration between public health workers and clinicians, developing health-promotion strategies, can improve the health outcomes for socially disadvantaged populations and can add more understanding of the mechanisms by which social determinants influence health.25 26
Despite the compelling evidence on the social determinant of health, very few large community interventions have been conducted worldwide. The landmark health initiatives conducted in Trieste over the past 50 years, afford a comprehensive approach to these issues, along with mental and paediatric health.27–29 Trieste lies at the extreme northeast of Italy, close to the borders with Austria and Slovenia. The area is mostly urban (inhabitants: 234,493; area: 212 km²; density: 1,107/km²; foreign nationality: 10% in 2019).30
In the last census conducted in Italy by the National Institute of Statistics in 2011, 27.6% of people residing in Trieste were over 65 years of age (vs 20.5% in Italy) and life expectancy at birth was 79 years for males and 83.6 years for females (vs 79.5 for males and 84.4 for females in Italy). In Trieste, the mortality rate for all causes was 14.5 per 1000 inhabitants (vs 10.0 per 1000 inhabitants in Italy) and the birth rate was 7.3 per 1000 inhabitants (vs 9.2 per 1000 inhabitants in Italy). Fifty per cent of the population was not in the labour force (vs 49.2 in Italy) and 4.7% were looking for a job (vs 5.8% in Italy); 52.7% of residents in Trieste had a low education level (vs 58.7% in Italy), 32.0% had a high school diploma (vs 30.2% in Italy) and 16.3% had a university degree or higher (vs 11.5% in Italy).30
The city has been, and still is, rich in contrasts and owes much of its centuries-old tradition of multilingualism and multiculturalism to its role as a port which, however, has also brought inequalities in the physical and social milieu and in health. In particular, at the beginning of the new millennium, an increase in population ageing, a prevalence of chronic conditions and polypharmacy, and inequalities in the distribution of risk factors and welfare reliance, including public housing, resulted in uncontrolled access to care explainable more in terms of social determinants and uncoordinated provision of medical care than of acute clinical progression demand. In particular, in Trieste, there are well-defined neighbourhoods known as ‘Microaree’, with 500 up to 2500 inhabitants, characterised by a high prevalence of social housing, economic and social hardship and poor environment quality.
To improve the health status and the social capital of these deprived communities, in 2006, the local health authorities, in conjunction with the voluntary and public social housing sectors and private citizens, implemented a proactive joint intervention programme called ‘Habitat Microaree’ (HM). The HM project started on 1 January 2006 in eight ‘Microaree’ and was designed to act both at the individual level, ensuring proper access to health facilities and social services, as well as improving the coordination of services; and at the community level, supporting hospital discharges. The HM project was conceived as a joint intervention delivered in people’s life setting and designed to act on multiple levels, health, social and housing, through a paradigm shift: services no longer as a set of a priori defined activities, but coproduced with people in order to engage them.31
In 2016, the University of Udine set up a retrospective cohort study to evaluate the effectiveness of this community-based social intervention, in terms of reduction of urgent admissions to both hospital and the ED, comparing subjects who lived in the microarea with subjects who lived in the neighbouring non-microarea quarters of Trieste. In conjunction and in coordination with this study, the University of Turin worked on the analysis of the social capital generated by the intervention in relation to the health status. Here, we present the results of the retrospective cohort study.
Methods
The HM project started on 1 January 2006 in eight ‘Microaree’ of Trieste accounting for a total of 11 380 residents. Eight multiprofessional teams were set up, one for each microarea, consisting of experts in continuum of care from the local health district, social workers from the municipality of Trieste and agents from the social housing agency.31 The HM activities to support the health and rights of citizens were linked to four intervention areas: (A) assessment of the priority health problems of the people residing in each microarea; (B) optimisation of interventions in support of home healthcare to prevent institutionalisation and improper hospitalisation; (C) promotion of collaboration between different institutions providing services to the same individual and on the same territory, through the active participation of the inhabitants and (D) fostering an active and participatory community. The close interrelationship and interdependence between socioeconomic factors, individual behaviours, the context of life and health make the reality of the Microaree extremely difficult to represent by classifying activities univocally in relation to specific objectives and areas of intervention. Table 1 shows some examples of the interventions delivered in the eight ‘Microaree’ of Trieste.
Table 1.
Aim | Purpose | Activity areas (examples) | Target |
Activities mainly aimed at health promotion, focusing primarily on health determinants. | Fostering the exercise of the right to citizenship | Providing orientation, assistance and support to families and individuals for access to health and social services and the fulfilment of procedures related to housing, employment and income support (simplify access to Offices and Agencies, Project In-town help desk, work placement grants, community service or socially useful work). | Adults, elderly, disabled, community |
Contributing to the respect of children’s right to education | Accompaniment to school. School support also for children with special educational needs, learning disabilities, (strengthen engagement with teachers and school institutions, after-school childcare services). |
Children | |
Developing community empowerment: Fostering intergenerational and interethnic knowledge and coexistence/integration |
Organisation of recreational and cultural group, community and intergenerational activities (libraries, reading and poetry; shows and movies; singing and music; old-fashioned and new games; excursions, exhibitions; parties and special events; language courses, courses on computer and cell phone use, arts and crafts courses, etc). | Children, adults, elderly, disabled, community | |
Involvement of asylum seekers and refugees in Microarea activities, as part of the convention with the Italian Consortium of Solidarity (ICS) | Adults | ||
Optimising the use of collective resources | Collection and distribution of unsold food items (food bank). Collection, maintenance, and distribution of toys, clothes, furniture, appliances, home devices (flea markets, charity shops) and other materials. |
Community | |
Courses on how to reuse and recycle materials. | Children, adults, elderly, disabled | ||
Activities mainly aimed at primary prevention to reduce the occurrence of diseases and injuries. | Combating isolation and loneliness | Ensure accessibility of microarea offices and/or other community spaces for group and community activities. Home visits and individual meetings. |
Children, adults, elderly, disabled |
Self-help groups (anxiety, violence, etc). | Adults, elderly, disabled | ||
Promoting the adoption of sustainable healthy lifestyles and encouraging socialisation | Organise meetings and classes to discuss issues related to lifestyles and health risk factors, also in collaboration with other local authority agencies, such as the Department of Prevention, Mental Health and Addiction Services and Voluntary Associations (Anonymous Alcoholics, Hiperyon, etc). Offer opportunities for intergenerational recreational, physical and sport activities (play and sport for children and teenagers, light exercise, dancing, walks, group on the move project, self-defence courses, etc.). Cooking courses. Care of the community garden. Preparation and consumption of meals (social breakfasts and lunches). |
Children, adults, elderly, disabled, community | |
Supporting vaccination campaigns | Raise the awareness of individuals, families and the community, also by organising dedicated meetings. | Children, adults, elderly, disabled, community | |
Activities primarily aimed at secondary prevention for early detection of diseases. | Improving access to regional screenings | Raise the awareness of individuals and the community, also by organising dedicated meetings. | Adults, elderly, disabled, community |
Activities mainly aimed at tertiary prevention to avoid the onset of complications or relapses following an illeness and/or at quaternary prevention to avoid the effects of hypermedicaliation. | Promoting home care for vulnerable people, avoiding institutionalisation | Provision of support and assistance to carry out day to day activites at home and outside home. Promote assisted cohousing and the development of supportive housing solutions. Provide information, orientation and support to caregivers (Alzheimer group…). |
Adults, elderly, disabled |
Promoting home care for vulnerable people, avoiding institutionalisation | Provision of support and assistance to carry out day-to-day activites at home and outside home. Promote assisted cohousing and the development of supportive housing solutions. Provide information, orientation and support to caregivers (Alzheimer group). |
Adults, elderly, disabled |
Adapted from: Il programma Habitat Microaree Trieste. Linee di indirizzo progettuali e operative.31
The study cohort and the associated variables of interest were extracted through record linkage with the administrative databases of the Regional Repository of MicroData of the Friuli Venezia Giulia region, using an anonymous identifier. The general population was made up by subjects who had lived in Trieste continuously in the 4 years preceding 2006. Based on the address of each subject on 1 January 2006, the general population was categorised as: (1) ‘resident in a microarea (M)’ 2) ‘non-resident in a microarea (NM)’. In order to make the two groups comparable, each M subject was matched with an NM subject through propensity score.32 33 We used the Nearest Neighbour Matching method with a greedy algorithm without replacement.34–36 The matching variables were: sex, the 2001 deprivation index by Caranci,37 age on 1 January 2006, the Charlson index38 constructed using hospital admissions in the 4 years preceding 1 January 2006, use of selected drugs in the year prior to 1 January 2006, identified according to the Anatomical Therapeutic Chemical classification system (ATC).39 The Caranci deprivation index is an estimate obtained by summing the standardised indicators of five traits, low level of education, unemployment, non-home ownership, one parent family and overcrowding that operationally combined represent the multidimensionality of the social and material concept of deprivation.37 The deprivation index by Caranci is available for each census block level in Italy. In our study, the categorised deprivation Caranci index was assigned based on the census block level of the subject’s residence. The Charlson index predicts the mortality risk of a patient who has had one or more hospital admissions for a range of comorbid conditions in a defined time period. For each identified comorbid condition a score is assigned, that depends on the risk of dying from that condition.38 We considered hypertension drugs (ATC: ‘C02’, ‘C03’, ‘C04’, ‘C07’, ‘C08’), diabetes drugs (ATC: ‘A10A’, ‘A10B’, ‘A10X’) and ulcer drugs (ATC: from ‘A02BC01’ to ‘A02BC05’, ‘A02BA’, ‘A02AA’, ‘A02AB’, ‘A02AC’, ‘A02AD’, ‘A02AF’, ‘A02AG’, ‘A02AH’, ‘A02AX’, ‘A02X’, from ‘A02BD01’ to ‘A02BD07’, ‘A02BB’, ‘A02BX’). We matched five ‘non-microarea’ subjects to each ‘microarea’ subject by propensity score. Out of the five ‘non microarea’ subjects, we selected the one whose residence was closer to the residence of the matched ‘microarea’ subject.
At the end of the matching process we obtained a cohort in which we considered as ‘participant’ to HM programme the subjects who lived in a microarea continuously during the follow-up period (microarea participant, MP), and as ‘non participant’ to HM programme the subjects who lived in a non-microarea for any length of time during the follow-up period (non-microarea participant, NMP). In order to maximise the differences between the participants to HM and the non-participants to HM, we focused our analysis only on stable residents, thus excluding individuals who alternated periods living in a microarea with periods living in a non-microarea. Furthermore, we considered the first 2 years as latency time. The follow-up of the resulting cohort, therefore, lasted from 1 January 2008 to 31 December 2015.
The study outcomes were first admission to a regional hospital, first admission to a local ED, multiple admissions to a regional hospital and to a local ED, during the follow-up period. The first admission to a regional hospital was identified as the earliest hospital admission for all causes, for each International Classification of Diseases ninth edition (ICD9-CM) diagnosis class, and for each specific diagnosis (ICD9-CM defined), during the study period. The date of the admission was defined as the ‘index date’ and each comorbidity was identified. The first admission to the ED was defined as the earliest ED admission for all causes occurring during the follow-up period, with the date of admission as the ‘index date’.
Admissions to regional hospitals were stratified in two groups: Ordinary (Planned+ Day hospital) and Urgent, while ED admissions were analysed according to triage priority codes: white (non-urgent conditions), green (minor injuries or illnesses), yellow (potentially life threating conditions) and red (life-threatening conditions). In the analysis, we also accounted for multiple hospital admissions and for multiple ED admissions. Multiple admissions were defined as repeated admissions of the same patient during the study period. We categorised multiple admissions in three classes: 0 admissions, 1 admission,≥2 admissions.
Participants and non-participants in the HM project intervention were compared in terms of first hospital admission and first access to ED, using Cox regression models. Person-time was calculated as difference between index date and beginning of follow-up. Multiple hospital admissions and ED accesses were analysed using ordered logistic regression models setting as reference the 0-category. All models were adjusted by age at the start of follow-up, by Charlson index and by the Caranci 2001 deprivation index and stratified by sex. The statistical software used for the analysis was the SAS software, V.9.4 (SAS Institute). This study was conducted in accordance with the 1964 Declaration of Helsinki and its later amendments.
Patient and public involvement statement
Anonymised patient data, from administrative databases, were used in this study; neither the patients nor the public were personally involved.
Results
At enrolment, the MP subjects were 10,588, and a corresponding number of matched NMP subjects was identified. The stable residents at the beginning of the follow-up period were a total of 16 256 (table 2).
Table 2.
MP (N=6963) | NMP (N=9293) | |||
Females | Males | Females | Males | |
n (%) | 3793 (54.5) | 3170 (45.5) | 5020 (54.0) | 4273 (46.0) |
Mean age (SD) | 57.7 (19.7) | 53.6 (19.8) | 54.5 (22.3) | 50.3 (20.6) |
The total follow-up time was 80 325.19 years, with mean value equal to 4.90 years (median=5.5 years; Q1=1.9 years; Q3=8 years). The HR that compares MP and NMP for first hospital admission for all causes was 0.95 (95%CI 0.91 to 0.99) while HRs for planned and urgent first admissions were, respectively, 0.97 (95%CI 0.91 to 1.02) and 0.95 (95%CI 0.90 to 1.01) (figure 1). Stratifying by gender, while in males, MP and NMP hazards for first admissions seemed to be broadly the same, in females the HR for first planned admission was 0.95 (95%CI 0.88 to 1.02) and for urgent admission was 0.92 (95%CI 0.85 to 1.00) (figure 2). When the analysis focused on the specific causes of hospitalisation, that is, by ICD9-CM diagnosis blocks, the HR of first urgent admission for mental disorders in females was 0.39 (95%CI 0.18 to 0.82). An increased, although not statistically significant, HR for planned admissions for mental disorders was also observed (HR 1.51; 95%CI 0.76 to 2.96) (figure 3). Again in females, the HR for first urgent hospitalisation caused by diseases of the genitourinary system was 0.74 (95%CI 0.49 to 1.11), whereas for planned admissions the HR was 1.03 (95%CI 0.82 to 1.31). Analysis of data on hospitalisation for diseases of the circulatory and respiratory systems showed a different pattern: HRs for circulatory system diseases were 1.15 (95%CI 0.98 to 1.35) for urgent hospitalisation, and 0.91 (95%CI 0.70 to 1.18) for planned admissions. HRs for respiratory system diseases were 0.95 (95%CI 0.74 to 1.21) for urgent and 0.63 (95%CI 0.42 to 0.94) for planned hospitalisations, respectively.
In males, the most relevant results concerns hospitalisation for diseases of the genitourinary system, with HR for first urgent admissions equal to 0.65 (95% CI 0.42 to 1.01), and for diseases of the circulatory system, with HR equal to 0.91 (95% CI 0.77 to 1.08) for first urgent hospitalisation and 1.37 (95% CI 1.08 to 1.74) for planned admissions (figure 4).
Focusing on the specific diagnoses, some relevant results emerged: in females, the HR for first urgent admission for psychosis (n.27; ICD9-CM 290–299) was equal to 0.15 (95% CI 0.05 to 0.51), while for acute respiratory infections (n.34; ICD9-CM 460–466) hour was 0.44 (95% CI 0.21 to 0.95). In males, the HR for first urgent admission for psychoses (n.21) was 0.49 (95% CI 0.19 to 1.27), and for other forms of heart disease (n. 197; ICD9-CM 420–429) 0.72 (95% CI 0.54 to 0.97). Regarding multiple admissions for all causes (table 3), the OR was 0.93 (95% CI 0.89 to 0.98) in females and 0.98 (95% CI 0.93 to 1.03) in males.
Table 3.
Multiple admissions | Participant | Sex | Frequency | % |
≥2 admissions | Microarea | F | 1318 | 23.9 |
M | 1103 | 20.0 | ||
Not microarea | F | 1732 | 31.4 | |
M | 1357 | 24.6 |
F, female; M, male.
For urgent hospitalisations (table 4), the OR was 0.95 (95% CI 0.90 to 1.00) in females and 1.03 (95% CI 0.96 to 1.09) in males.
Table 4.
Multiple admissions | Participant | Sex | Frequency | % |
≥2 admissions | Microarea | F | 681 | 23.7 |
M | 607 | 21.2 | ||
Not microarea | F | 886 | 30.9 | |
M | 695 | 24.2 |
F, female; M, male.
Of particular relevance was the OR for multiple urgent admissions for fractures (ICD9-CM 800–829) in females, equal to 0.75 (95% CI 0.58 to 0.97). Analysing hazards for first access to ED, a slight reduction emerged for white codes, both in females and in males; the HRs were, respectively, 0.97 (95% CI 0.89 to 1.05) and 0.94 (95% CI 0.86 to 1.03). This reduction was found also for green codes but only in females: HR 0.94 (95% CI 0.87 to 1.00). For other priority codes, no risk differences emerged (data not shown). For what concerns multiple accesses to ED, again a minor reduction emerged for white codes both in females and in males, with ORs, respectively, equal to 0.97 (95% CI 0.91 to 1.02) and 0.97 (95% CI 0.92 to 1.03), and for green codes, but only in females, with OR equal to 0.95 (95% CI 0.91 to 1.00). No further significant results emerged for other priority codes (data not shown).
Discussion
We focused on the hazards of first hospitalisation as main measurable outcomes, under the hypothesis that after the first hospital access patients are more likely to be involved in a controlled clinical follow-up, and therefore, subsequent hospital admissions may not be independent events. Our results show a slight reduction in hazard of first hospitalisation for all causes in MP. For urgent admissions in females, the reduction appears to be more pronounced. Similarly, hazards for first access to ED for the lowest priority access code, both in females and in males, seem to be slightly decreased. This reduction was found also for green codes but only in females, while for other priority codes, no risk differences emerged. In the literature, interventions such as patient education, needs assessment, telephone support and follow-up have been shown to effectively reduce hospital admissions.40 A meta-analysis by Panagioti et al41 showed that interventions aimed at improving self-management support, reduced health services utilisation, with no negative impact on patient health outcomes; in particular, robust evidence in this sense was found for respiratory and cardiovascular disorders. Coherently with these results, in our study, MP females, showed a lower risk for acute respiratory infections, while in MP males, a lower risk of first urgent hospitalisation for ‘other forms of heart disease’ was observed. However, the most remarkable finding that emerged from our study concerns psychosis, particularly in females. The longitudinal SMILE study in the Netherlands42 has shown that persons reporting material deprivation were at higher risk of physical and mental disorders. In a meta-analysis of the effect of early interventions for psychosis, Randall et al43 describe a positive effect in terms of hospitalisation reduction. McFarlane et al44 noted that admission rates for psychotic episodes were reduced by a community-wide programme of early identification and intervention initiated in 2001.
Multiple admissions represent a patient safety concern as well as a public cost.40 Socioeconomic status is strongly associated with hospital outcome measures and there is evidence showing that some multifaceted interventions can successfully reduce hospital readmissions.45 In a randomised control trial carried out between 1992 and 1996, Naylor et al46 studied the effectiveness of nurse-centred discharge planning and follow-up intervention for subjects at higher risk of readmission. Twenty-four weeks after hospital discharge, readmission was more frequent for patients in the control group than in the intervention group.
Our results also suggest that the HM project was effective in reducing multiple admissions for all causes in females (table 3), and particularly for fractures.
For what concerns ED care services, there is evidence of an increased demand in countries where population ageing generates more diverse and complex care needs.47 Factors such as lack of access to affordable primary care around-the-clock and lack of awareness of available services or of diagnostic and therapeutic protocols, explain why the demand for these services is persistently increasing. In addition, patients of low socioeconomic status tend to prefer hospital care to primary care, because hospital care is perceived as higher quality and more convenient and accessible.48 Our results show that during the multifaceted HM project, the hazards of first access to ED for white codes slightly decreased, both in females and in males.
Our study presents some limitations: our data derive from administrative databases through an anonymous identifier, therefore, although in actual facts not all residents were directly involved in the HM project, for the purposes of our analysis, all residents in the selected microareas were considered as participants in the HM project. This may have introduced a certain degree of misclassification with a likely underestimation of the effectiveness of the intervention. Moreover, between 2009 and 2012, the HM project was extended to a further three microareas, therefore, among those whom we considered non-participants, there were residents who were in fact involved in the intervention. Again, this might have contributed to underestimate the effectiveness of the intervention. Our results suggest that the HM programme was more effective with females; based on the reports of the multiprofessional teams, a possible explanation may be that it was easier to involve females than males. This, however, represents a limitation in terms of results generalisability.
Our study also presents a number of strengths: it involved a wide cohort for a long follow-period and the use of administrative databases provided a complete picture of the subjects’ access to healthcare facilities, diagnoses, therapies and procedures during the study period. To our knowledge, this is one of few studies that evaluate the effectiveness of a social intervention in terms of impact on health services. In our view, this study may represent the starting point for a more comprehensive assessment aimed at determining the impact of the HM project on the healthcare system also in terms of costs, a topic of significant interest since sustainability of the public health service is a matter of great current concern.
Conclusions
Our results show that by acting on the social determinants of health, the burden on the health service can be controlled and reduced. Our evidence shows that during the follow-up period, there was a reduction of first urgent hospital admissions in the social intervention area, especially in females and for specific diagnoses such as psychosis. Also multiple admissions were decreased in the intervention group, again, mainly in females and for specific diagnoses such as fractures.
Supplementary Material
Acknowledgments
The authors thank all the representatives of the 'Habitat Microaree' project for their valuable work.
Footnotes
Contributors: LC, FB, MGC-D and FP conceived, designed and coordinated the study. MS, EA, CE and FP collected data. MG, LC and VR defined the statistical analysis plan and performed the analysis. LC, MG, FB, MGC-D and FP interpreted the results. LC and MG drafted the paper. FB, MGC-D, MS, EA, CE, FP and VR critically revised the manuscript.
Funding: This retrospective cohort study was supported by a fund allocated by the local health authority of Trieste 'Azienda Sanitaria Universitaria Integrata di Trieste' on 31 August 2016 (CUP E97B16000340002) through an ad hoc agreement with the University of Udine. Researchers acted independently from the funder and all authors had full access to all data (including statistical reports and tables) in the study and can take responsibility for the integrity of the data and the accuracy of the data analysis.
Competing interests: None declared.
Patient and public involvement: Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Patient consent for publication: Not required.
Ethics approval: This study did not require ethical approval since data were extracted from the administrative databases of the Regional Repository of MicroData using an anonymous identifier.
Provenance and peer review: Not commissioned; externally peer reviewed.
Data availability statement: No data are available. All data relevant to the study are included in the article or uploaded as online supplementary information.
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