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PLOS Neglected Tropical Diseases logoLink to PLOS Neglected Tropical Diseases
. 2018 Jun 13;12(6):e0006577. doi: 10.1371/journal.pntd.0006577

The role of social determinants of health in the risk and prevention of group A streptococcal infection, acute rheumatic fever and rheumatic heart disease: A systematic review

Pasqualina M Coffey 1,*, Anna P Ralph 2,3, Vicki L Krause 1
Editor: James S McCarthy4
PMCID: PMC6016946  PMID: 29897915

Abstract

Background

Rheumatic heart disease (RHD) poses a major disease burden among disadvantaged populations globally. It results from acute rheumatic fever (ARF), a complication of Group A Streptococcal (GAS) infection. These conditions are acknowledged as diseases of poverty, however the role of specific social and environmental factors in GAS infection and progression to ARF/RHD is not well understood. The aim of this systematic review was to determine the association between social determinants of health and GAS infection, ARF and RHD, and the effect of interventions targeting these.

Methodology

We conducted a systematic literature review using PubMed, the Cochrane Library and Embase. Observational and experimental studies that measured: crowding, dwelling characteristics, education, employment, income, nutrition, or socioeconomic status and the relationship with GAS infection, ARF or RHD were included. Findings for each factor were assessed against the Bradford Hill criteria for evidence of causation. Study quality was assessed using a standardised tool.

Principle findings

1,164 publications were identified. 90 met inclusion criteria, comprising 91 individual studies. 49 (50.5%) were poor quality in relation to the specific study question. The proportion of studies reporting significant associations between socioeconomic determinants and risk of GAS infection was 57.1%, and with ARF/RHD was 50%. Crowding was the most assessed factor (14 studies with GAS infection, 36 studies with ARF/RHD) followed by socioeconomic status (6 and 36 respectively). The majority of studies assessing crowding, dwelling characteristics, education and employment status of parents or cases, and nutrition, reported a positive association with risk of GAS infection, ARF or RHD. Crowding and socioeconomic status satisfactorily met the criteria of a causal association. There was substantial heterogeneity across all key study aspects.

Conclusion

The extensive literature examining the role of social determinants in GAS infection, ARF and RHD risk lacks quality. Most were observational, not interventional. Crowding as a cause of GAS infection and ARF/RHD presents a practical target for prevention actions.

Author summary

Rates of rheumatic heart disease (RHD) are high in disadvantaged populations globally. It results from acute rheumatic fever (ARF), a complication of Group A Streptococcal (GAS) infection. These are described as diseases of poverty, but exactly what components of poverty promote them has been unclear. The aim of this review was to find what specific social and environmental factors are associated with GAS infection, ARF and RHD, and if actions targeting these can reduce disease rates. We did a search of published literature and found 90 relevant articles. Many supported an association between GAS infection, ARF or RHD and crowding, dwelling characteristics, low education level and employment status, poor nutrition and low social class. There was enough evidence to show that crowding and socioeconomic disadvantage increase the risk of GAS infection and ARF/RHD. However, most studies were of fair to poor quality in their ability to answer the research question, and there was little interventional research. This may relate to challenges inherent in intervening to change social determinants of health, but may also suggest lesser research attention to health issues affecting disadvantaged populations. The association between crowding and disease risk strongly supports initiatives to reduce crowding. This should become a key target for ARF and RHD prevention.

Introduction

Rheumatic heart disease (RHD) is an important cause of cardiac morbidity and mortality in disadvantaged populations globally [14]. It results from acute rheumatic fever (ARF), which itself occurs as an abnormal immunological response to Group A Streptococcal (GAS) infection of the throat (streptococcal pharyngitis) and possibly streptococcal skin infection[5] in susceptible hosts [6]. GAS pharyngitis is spread through direct person-to-person transmission via saliva or nasal secretions [7]. Generally very few people will develop ARF after GAS exposure, but it may be as high as 5 to 6% in certain groups with greater susceptibility and heavy GAS exposure [8]. Recurrences of ARF cause progressive valvular damage, with between 50 and 75% of cases progressing to RHD [8]. RHD is a chronic and debilitating condition characterised by complications such as arrhythmias and heart failure [6]. ARF and RHD most often affect children and young adults [2]. The true burden of the disease is expected to be far higher than the benchmark estimates, but even at conservative calculations, it is equivalent to approximately one quarter of the global DALY burden of cancer [3].

Globally, ARF and RHD are almost exclusively seen in developing nations or among disadvantaged populations within developed nations [2]. Among populations safeguarded by high standards of living, RHD rates are virtually zero. This dramatic contrast highlights the influence of environmental, economic, social and behavioural conditions on risk of GAS infection and progression to ARF and RHD. Despite the role of social determinants of health in disease genesis, key RHD control programs and guidelines[4, 9, 10] do not specifically address primordial prevention. Primordial prevention aspires to establish and maintain conditions to minimize hazards to health. It consists of actions and measures that inhibit the emergence and establishment of environmental, economic, social and behavioural conditions, cultural patterns of living known to increase the risk of disease[11]–that is, strategies that aim to eliminate exposure to risk factors in the first place. Current strategies focus on primary prevention (early detection and treatment of GAS infections), secondary prevention (delivering intramuscular penicillin every four weeks) and tertiary prevention (medical and surgical management of heart failure) [12]. These cornerstones of RHD control are heavily reliant on health care services being available and accessible, a sufficient level of health literacy and appropriate health seeking behaviour among the general population, and ongoing commitment from cases to receive their injections. However, in settings of poverty or marginalisation, these elements cannot be guaranteed. Furthermore, medical treatment and case management can reduce morbidity and mortality, but they will not change the underlying risk to vulnerable populations [13].

Therefore primordial prevention should be part of a comprehensive strategy to eliminate RHD as a public health problem–a global goal [14]. But while ARF and RHD are generally referred to as ‘diseases of poverty’,[14] there is uncertainty about what specific aspects of poverty create the conditions that cause RHD. In order to implement evidence-based preventive strategies at the primordial level, more needs to be understood about the relative contribution of the individual components of poverty, such as household crowding, educational attainment, employment, income, nutrition and overall socioeconomic status to RHD risk. Additionally, evidence for any public health interventions targeting these primordial-level factors needs evaluating.

To provide the evidence base for primordial-level preventative interventions to control RHD, we undertook a systematic review with two aims: to determine the association between social determinants of health and GAS infection, ARF and RHD, and to determine the effect on GAS infection, ARF and RHD of interventions targeting these determinants.

Methods

Search strategy

We conducted a systematic literature review on the association between socioeconomic and environmental factors and GAS infection, ARF or RHD, and on the impact of interventions targeting these factors.

The search was conducted between August and October 2016 and eligible articles were identified by searching three databases: PubMed, Cochrane Library and Embase. MeSH terms, key words and Emtree terms (Embase thesaurus headings) searches were conducted. See S1 Table for full details of the search strategy.

All titles and available abstracts were screened by one author (PC). Articles were eligible for inclusion in the analysis of interventions if they were in English, reported on an intervention that encompassed: health promotion, education, or behaviour change targeting social determinants of GAS infection (including impetigo), ARF, or RHD; the provision of hygiene hardware, aids or household infrastructure; or household crowding reduction. Interventions could be at an individual, household, health centre, school or community level. Inclusion criteria for observational studies were that they must have reported on at least one socioeconomic or environmental variable and its relationship with GAS infection including impetigo), ARF or RHD incidence or prevalence, measured objectively at an individual, ecologic or population level with a comparison group (either study controls or use of population data e.g. census). Studies were excluded: if they were not in English; assessed pharmacological interventions only; were of very poor quality; or provided only a subjective appraisal of or no description of methods for ascertaining socioeconomic and environmental factors. No restrictions were set with regards to date of publication. Factors specified in the search strategy included: crowding (household or other settings), income, dwelling characteristics, education level, occupation/employment, social class, and nutrition. These were chosen through a scoping scan of selected literature sources informed by the authors’ prior knowledge in this area. There were no limitations on participant age, setting, geographic location or publication date of the studies. References of selected studies were searched for further articles not covered in the primary search strategy.

The primary outcome was reduction in GAS infection, ARF, or RHD from an intervention targeting a socioeconomic or environmental factor. The secondary outcome was evidence of a causal relationship or association of GAS infection, ARF or RHD with specific social determinants of health.

The full text of the articles were reviewed by the same author (PC) and data were extracted to a template that included information on article details (title, year, first author), study type, study methodology, participants and setting, outcomes, and additional notes including salient points from the discussion or authors' conclusions. Study quality and risk of bias pertaining to measurement of determinants and outcomes of interest to this review were assessed for each study using the National Institute of Health Study Quality Assessment Tool,[15] with the appropriate template used based on the study type (S1 Text). Ecologic studies were judged on additional criteria as described in Dufault and Klar (2011) [16]. Study quality as relevant to this review was rated as: very poor (subsequently excluded), poor, fair, fair to good and good.

Descriptive analysis

Descriptive analysis involved recording the frequency of specific factors measured across the studies and whether a statistically significant association with GAS infection, ARF or RHD was identified, the direction of the association (considered positive if greater degrees of the factor of interest were associated with higher disease rates), mixed, negative, possible or not found. A p value of <0.05 was used to define a statistically significant association. ‘Possible’ designated a reported positive association where a test of significance was not provided, nor means to calculate one. ‘Mixed’ designated a combination of positive, negative or absence of association for different measures of the same variable. Results for GAS infection were presented separately and ARF/RHD to reflect the different epidemiology and natural history of the conditions.

The findings were synthesised in the context of study quality and strengths and limitations of findings. Systematic reviews (n = 4) were reviewed for quality and findings separately.

The evidence of the link between each of the main factors explored and GAS infection, ARF and RHD was assessed against the Bradford Hill criteria, a set of nine guiding principles for interpreting causal relationships between environmental influences and disease. The criteria are: strength of association, consistency, temporality, biological gradient, plausibility, coherence, experiment, specificity and analogy [17].

Statistical analysis

The studies were too heterogeneous in exposure and outcome measures for meta-analysis.

In some instances where statistical testing was not performed in the original study, but enough data were presented to allow analysis to be undertaken (i.e. a 2 X 2 table with denominators), simple tests of significance (chi-squared, odds ratio (OR) with 95% confidence intervals, or relative risk (RR)) were calculated using the Tables for Epidemiologists function in Stata 13.1 (Statacorp, Texas 2013). These additional analyses are indicated in S2S8 Tables.

Statistical analysis was conducted to check for correlation of study type, quality of study (fair or greater), outcome of interest (GAS infection, ARF or RHD) and positive outcomes using chi-squared and Fisher’s exact tests of significance. Correlation between year of publication and study quality was analysed using binomial variables of published in previous 20 years (>1996) and study quality equal to or greater than fair. Analysis was carried out using Stata 13.1 (Statacorp, Texas 2013).

This review adheres to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) checklist (S1 Checklist) [18].

Results

Overview

The search strategy identified 1,164 articles in PubMed, 273 articles in Embase and 84 articles in the Cochrane Library (S1 Fig). An additional 21 study articles were recovered from manual reference searches of the selected articles. Of these 114 were selected on the basis of title and abstract. The full text was unavailable for eight articles. The full texts of the remaining articles were reviewed and of these one article was excluded due to being very poor quality as were two studies from an article [19] of three studies were excluded. Hence 90 articles met the inclusion criteria comprising 91 individual studies included in the general analysis, as one article contained two separate studies (Table 1) [20].

Table 1. Summary of included studies with outcome of GAS infection, including findings, study type and quality assessment.

Crowding Dwelling characteristics and facilities Education Employment Income Nutrition Socioeconomic status
Number of studies, n 14 7 1 0 3 0 6
Association with GAS infection, n (%)  
Positive 6 (42.9) 4 (57.1) 0 (0.0) NA 1 (33.3) NA 3 (50.0)
Mixed 2 (14.3) 0 (0.0) 0 (0.0) 1 (33.3) 0 (0.0)
Possible 1 (7.1) 0 (0.0) 0 (0.0) 1 (33.3) 0 (0.0)
No association 5 (35.7) 3 (42.9) 1 (14.3) 0 (0.0) 3 (50.0)
Study type, n (%)  
Case control 1 (7.1) 0 (0.0) 0 (0.0) NA 0 (0.0) NA 0 (0.0)
Case series 1 (7.1) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Cohort 6 (42.9) 2 (28.6) 0 (0.0) 1 (33.3) 2 (33.3)
Control trial 1 (7.1) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Cross section 4 (28.6) 2 (28.6) 1 (14.3) 2 (66.7) 2 (33.3)
Ecologic 1 (7.1) 0 (0.0) 0 (0.0) 0 (0.0) 2 (33.3)
Randomised control trial 0 (0.0) 3 (42.9) 0 (0.0) 0 (0.0) 0 (0.0)
Quality assessment, n (%)  
Good 1 (7.1) 1 (14.3) 0 (0.0) NA 0 (0.0) NA 1 (16.7)
Fair to good 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 1 (16.7)
Fair 2 (14.3) 1 (14.3) 0 (0.0) 0 (0.0) 1 (16.7)
Poor to fair 3 (21.4) 2 (28.6) 0 (0.0) 1 (33.3) 2 (33.3)
Poor 8 (57.1) 3 (42.9) 1 (14.3)   2 (66.7)   3 (50.0)

Several articles were based on the same study population. Two articles by McDonald et al.(2006) [21] (2008) [22] shared the same participants and a third, a subset of these [5]. The articles authored by Adanja et al.(1988) [23] (1991) [24] and Vlajinac et al. (1989) [25] (1991) [26] utilised the same participants, as did two studies by Zaman(1998a) [27] (1998b) [28]. Four systematic reviews were analysed separately [2, 2931].

33 studies reported ARF as the outcome, 27 reported RHD, 10 reported both, and 21 reported GAS infection. There were 16 case control studies, [2328, 3241] nine case series, [4250] 12 cohort studies, [5, 21, 5161] one control trial, [62] 28 cross section studies, [19, 6389] 22 ecologic studies, [20, 90105] and three randomised controlled trials (RCT) [106108]. Studies were conducted in 27 countries with two studies including data from multiple countries.

The quality of the studies in design or ability to answer the research question was rated as poor in 45 (50.5%). Only three studies graded as being of good quality. Studies that were case series were most likely to be of poor quality. Two of the three RCTs, seven of 16 (43.8%) case control, and five of 12 (41.7%) cohort studies were of at least fair quality. Studies published after 1996 (25 of 37) were more likely to be of fair or better quality than those published earlier (6 of 54) (OR 16.7, 95% CI 5.59 to 49.71). Study quality was not associated with outcomes.

12 studies (57.1%) reported a positive relationship between at least one socioeconomic factor and risk of GAS infection, and 35 studies (50.0%) reported a positive relationship between a socioeconomic factor and risk of either ARF or RHD.

The likelihood of positive findings was not associated with publication after 1996 or study quality. 100% of the case control studies reported at least one positive association of a socioeconomic factor with disease rates compared to 64.9% of other studies (Fisher’s exact p = 0.002).

Crowding

50 studies assessed the association between crowding and GAS infection (14 studies), ARF (16 studies), RHD (15 studies) or a combination (5 studies) (Tables 1 and 2; S2 Table). The most common measures of crowding were: persons per household, room, bedroom or bed; number of children or siblings; dwelling space; and sleeping space per person. 12 of 21(57.1%) studies noted a positive association between crowding and the different outcomes of GAS infection, 9 of 16 (56.3%) with ARF, and9 of 15 with RHD (60.0%) and combinations thereof (60.0%), though only 14 found consistent associations across all measures of crowding (42.9% among studies of GAS infection and 30.6% among ARF/RHD). A further 10 studies reported a possible association between crowding and GAS infection, ARF or RHD risk but did not provide a test of significance nor means to calculate one.

Table 2. Summary of included studies with outcome of ARF and/or RHD, including findings, study type and quality assessment.

Crowding Dwelling characteristics and facilities Education Employment Income Nutrition Socioeconomic status
Number of studies, n 36 19 16 15 18 15 36
Association with ARF/RHD, n (%)  
Positive 11 (30.6) 6 (31.6) 4 (21.1) 5 (33.3) 6 (33.3) 4 (26.7) 16 (44.4)
Mixed 10 (27.8) 6 (31.6) 6 (31.6) 3 (20.0) 1 (5.6) 8 (53.3) 2 (5.6)
Possible 9 (25.0) 1 (5.3) 0 (0.0) 2 (13.3) 2 (11.1) 1 (6.7) 10 (27.8)
No association 6 (16.7) 6 (31.6) 6 (31.6) 5 (33.3) 9 (50.0) 2 (13.3) 8 (22.2)
Study type, n (%)  
Case control 12 (33.3) 10 (52.6) 9 (47.4) 7 (46.7) 9 (50.0) 7 (46.7) 4 (11.1)
Case series 3 (8.3) 1 (5.3) 1 (5.3) 0 (0.0) 2 (11.1) 1 (6.7) 4 (11.1)
Cohort 3 (8.3) 2 (10.5) 1 (5.3) 3 (20.0) 1 (5.6) 1 (6.7) 1 (2.8)
Control trial 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Cross section 11 (30.6) 5 (26.3) 2 (10.5) 3 (20.0) 2 (11.1) 5 (33.3) 14 (38.9)
Ecologic 7 (19.4) 1 (5.3) 3 (15.8) 2 (13.3) 4 (22.2) 1 (6.7) 13 (36.1)
Randomised control trial 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Quality assessment, n (%)  
Good 1 (2.8) 0 (0.0) 0 (0.0) 0 (0.0) 1 (5.6) 0 (0.0) 1 (2.8)
Fair to good 4 (11.1) 4 (21.1) 3 (15.8) 1 (6.7) 3 (16.7) 3 (20.0) 1 (2.8)
Fair 10 (27.8) 3 (15.8) 5 (26.3) 6 (40.0) 3 (16.7) 5 (33.3) 11 (30.6)
Poor to fair 6 (16.7) 3 (15.8) 3 (15.8) 3 (20.0) 2 (11.1) 2 (13.3) 4 (11.1)
Poor 15 (41.7) 9 (47.4) 5 (26.3) 5 (33.3) 9 (50.0) 5 (33.3) 19 (52.8)

1Note studies may appear more than once if they assessed more than one factor e.g. crowding and education.

Of the 11 studies that assessed crowding after adjusting for one or more independent variables such as household income, seven noted a residual association between crowding and the outcome of interest. Two case control and three ecologic studies demonstrated a continuous effect gradient between crowding and risk of GAS infection, [38] ARF, [41, 90, 109] and RHD [96].

The remaining 11 (22%) studies that examined an association between crowding and disease rates did not demonstrate any association between crowding and disease risk.

Dwelling characteristics and facilities

Dwelling characteristics and facilities were assessed across a variety of measures such as general housing condition, construction type, specific characteristics (e.g. dampness, ventilation), or facilities (e.g. water, electricity, toilets) in relationship to GAS infection in seven studies and ARF/RHD in 19 (Tables 1 & 2; S3 Table). Four of seven studies reported positive or mixed associations between dwelling characteristics or facilities with increased GAS infection rates, eight of nine with ARF, two of eight with RHD, and both of the studies that assessed ARF and RHD together. General poor condition or standard of housing was associated with increased risk of ARF or RHD in five of nine studies and type of housing construction or material was associated with GAS infection, ARF or RHD risk in six of nine. Home dampness was associated with ARF in five of seven studies (three of these analysed the same population). There were no clear trends among other specific housing characteristics and facilities (e.g. electricity, kitchen facilities, light, potable water, sewerage, and ventilation) and GAS infection or ARF/RHD.

Three diverse RCTs assessed interventions aimed to induce or reduce acquisition of GAS or its sequelae through common household fomites [106, 108] or hygiene practices [107]. Of these only Luby et al’s (2005) RCT demonstrated an effect on GAS related disease (impetigo). Over 4,600 children were randomised to receive hand washing promotion and antibacterial soap, hand washing promotion and plain soap, or no intervention. The mean impetigo incidence was 36% and 24% lower among the antibacterial and plain soap groups compared to the control group respectively.

Education

The education level of mothers, fathers and cases themselves were explored across 17 studies, with 16 studies reporting ARF/RHD as the outcome (Tables 1 & 2; S4 Table). Low maternal education or literacy was positively associated with ARF incidence in two of three studies, though these two studies shared the same population [23, 25]. Two studies [26, 46] reported results of multivariable analyses and found that maternal education remained associated with ARF after adjusting for other variables. Low maternal literacy was associated with both ARF and RHD in another study [35] and RHD prevalence in one [56] of two studies, [33] but this relationship did not hold in multivariate analysis. There were no clear trends for education levels of fathers, parents combined, or of cases with any of the outcomes.

Employment

The relationship between employment and ARF/RHD was explored in 15 studies. No studies examined relationship between employment and risk of GAS infection (Tables 1 & 2; S5 Table). Maternal employment was considered a marker of social or economic disadvantage rather than advantage in four studies. In these studies, maternal employment was positively association with ARF in two of two studies, [23, 41] and with both ARF and RHD in another study, [35] but was not associated with RHD risk in Mirabel et al’s study (2015) [56]. In contrast, a Fijian based case control study measured maternal employment as a marker of socioeconomic advantage and found maternal unemployment was associated with RHD prevalence [33]. There were no associations in any of the five studies that assessed paternal employment [33, 35, 41, 54, 65]. Employment status (unemployment/low class occupation) of the case was found to be associated with RHD in three [40, 61, 76] of four studies [72].

Findings of the three studies that reported GAS infection risk and low income were diverse (Table 1; S6 Table). For ARF/RHD, six of 18 studies reported a positive relationship with low income, while nine demonstrated no association (Table 2). In three studies that undertook multivariate analyses, a positive association was retained in one, [90] but lost in two [36, 40].

The method of assessing income (strata, a binomial measure or comparison of mean income) did not affect the likelihood of reporting an association.

Nutrition

15 studies (covering 12 separate study populations) assessed the relationship between nutrition and ARF or RHD using either dietary intake or anthropometric measures (Tables 1 & 2; S8 Table). Four (26.7%) reported only significant associations between nutritional impairment and ARF or RHD, though tended to only report one simple measure (e.g. low weight or BMI) [26, 74]. A further eight (53.3%) studies demonstrated mixed results.

Socioeconomic status

The relative social position of cases compared to non-cases or to the general population was based on geographical, economic, occupational and social factors, or was based on the ownership of specific assets. Socioeconomic status (SES) or social class was assessed in six studies reporting GAS infection as an outcome, and 36 studies reporting ARF/RHD, with three (50%) and 16 (44.4%) respectively showing a definite association (Tables 1 & 2; S8 Table). A further 10 studies showed a possible association between lower social class with ARF/RHD (i.e. studies that did not provide a statistical test of the apparent relationship between ARF and RHD); nearly all had ecologic designs. 10 studies were able to demonstrate a clear gradient of social class and GAS infection,[20] ARF[87, 90] or RHD[63, 67, 71, 77, 98, 110] risk, with several others suggestive of a gradient.

Systematic reviews

Four systematic reviews of risk factors for GAS infection, ARF or RHD were identified [2, 2931]. Only one used a systematic search method for social and environmental risk factors for GAS infection, ARF or RHD [29] and none identified the number of studies found for inclusion in the present review. All four reviews explored SES or poverty in some way. In addition, Kerdemelidis et al (2010) [29] and Steer et al (2002) [30] reviewed crowding, nutrition, and housing factors. The quality of the four studies ranged from poor to fair according to our criteria for measurement of determinants and outcomes of interest to this review, and no review produced firm conclusions.

Factors assessed against the Bradford Hill Criteria

Each socioeconomic or environmental factor was assessed against the Bradford Hill criteria to establish whether a causal relationship with RHD and its antecedents was supported by the evidence contained in this review (Table 3). Crowding provided a sufficient weight of evidence across the criteria to support a causal relationship, as did socioeconomic status to a lesser extent.

Table 3. Bradford Hill criteria for evidence of causation as applied to the relationship of GAS infection, ARF and RHD with social determinant factors.

Criteria Crowding Dwelling characteristic and facilities Education Employment Income Nutrition Socioeconomic status
Strength Between 1.7 and 2.8 fold risk across various measures of crowding Between 2.3 and 3.5 fold risk with dampness; 1.8 to 3.6 fold risk with poor construction/material type.
Small number of studies reporting strength for other measures
Between 1.7 and 3.9 higher odds of disease with low maternal literacy Small number of studies reporting strength with wide distribution Small number of studies reporting strength Between 1.4 and 2.7 fold risk for underweight.
Small number of studies reporting strength for other measures
Range between 1.5 and 5 fold risk among lowest SES compared to middle and high SES groups
Consistency 29/50 (58%) reported positive associations across many study types 16/26 (61.5%) reported positive associations No No No No Yes: when clear measures of SES assessed
Temporality Yes: factor likely to be longstanding Yes: factor likely to be longstanding Yes: education of mother or father precedes life of child Yes: for employment of parents, not necessarily for case Yes: factor likely to be longstanding Unknown: Chronic RHD could contribute to poor growth in children. Yes: factor likely to be longstanding
Biological gradient Yes: 5 studies No No No Yes: 1 study No Yes: 10 studies
Plausibility Yes: GAS spread via close contact No plausible mechanisms discussed for dwelling characteristics.
Use of soap is an effective means for removing microorganisms from hands and body.
Yes: maternal literacy impacts on hygiene practices, care-seeking and treatment behaviours Indirectly: unemployment/lower class employment relates to income, access to health care etc. Yes: income impacts on access to health care services and material conditions Yes: nutritional deficiencies are associated with poor immune response to infection Indirectly: social class relates to income, access to healthcare and living conditions.
Coherence Yes Insufficient evidence Yes Insufficient evidence Yes Yes Yes
Experiment No Mixed results-soap reduced impetigo; fomite intervention did not change GAS acquisition. Nil for dwelling characteristics No No No Yes-very poor quality No
Specificity No No No No No Dietary supplementation with eggs was reported to be associated with lower ARF case numbers No
Analogy Meningococcal disease [111113] and respiratory syncytial virus [114116] Housing improvements improve respiratory health[117] Increased maternal literacy associated with decreased child diarrhoeal disease, fever and respiratory infection [118] Higher adult mortality rate among lower employment grades [119] Adult mortality rate and income [120] Childhood malnutrition has strong relation with risk of death from diarrhoeal and acute respiratory infections [121] Higher odds of neglected tropical diseases among socioeconomically disadvantaged groups[122]

ARF: Acute rheumatic fever GAS: Group A Streptococcus SES: Socioeconomic status

The strengths of the observed relationships of crowding and outcomes were modest; odds ratio or relative risk calculations for binary outcomes (i.e. crowded vs. not crowded whether at a bed, bedroom or housing level) produced around a twofold likelihood or risk of GAS infection, ARF and RHD. In Jaine et al’s ecologic study of ARF cases across New Zealand, after adjusting for average income and number of children aged 5–14 years, the authors noted that a 1% increase in the proportion of households defined as being crowded conferred a 6.5% increase in the expected ARF count at a census area unit level [90].

Regarding consistency, 29 of the 50 studies that assessed crowding reported statistical evidence of an association with GAS infection, ARF or RHD risk. Further studies demonstrated an apparent relationship but did not conduct any significance testing.

The necessary criteria of temporality between cause and effect was met.

While an individual may experience housing instability or change, the characteristics relevant to crowding, e.g. amount of bedrooms a family can afford, is not likely to change greatly during an individual’s childhood [23, 98]. Therefore a point in time capture of data (as in a cross-sectional study) would be likely to represent the living conditions that a case was subject to prior to the development of the condition. As previously described 5 studies demonstrated a gradient in the relationship between crowding and GAS infection, ARF or RHD [38, 41, 90, 96, 109].

The biological mechanism by which crowding exerts its effect on ARF and RHD is via its relationship to GAS acquisition. Crowding fosters intimate contact and consequent GAS transmission directly by human-to-human contact and via droplet spread [123]. Higher GAS infection rates increase the chance that from any one event ARF sequelae will develop. The role of household crowding as the chief driver of GAS transmission was demonstrated in Levine et al’s large cohort study (1966) [38]. Here, GAS infections were not randomly distributed throughout the cohort but clustered within discrete family units as evidenced by high serological concordance between positive family members. The cause and effect interpretation of crowding and GAS acquisition coheres with our knowledge of the natural history and biology of these conditions.

There were no experimental studies assessing crowding and GAS infection, ARF or RHD risk. The closest such evidence comes from findings of an US Air Base Streptococcal Laboratory [50]. This group reported higher acquisition rates of GAS in new army recruits relating to the vicinity of their bed to a known GAS carrier and the amount of carriers within each barracks. In this study, rates of GAS acquisition in new (unexposed) recruits was documented in relation to their distance from the untreated colonised index case, showing a gradient effect; closer proximity was associated with higher risk, giving the study an almost quasi-experimental design. However, this study failed to test whether an intervention against crowding (i.e. actively moving beds further away) was an effective means of decreasing GAS transmission.

Crowding does not exhibit specificity for GAS infection and its sequelae. It is an established health risk for transmissible diseases, especially of those with epidemic potential where outbreaks are more frequent and more severe when the population density is high [124]. An analogy to the droplet transmission of GAS and its predilection among children are offered by the firm observations of the link between crowding and meningococcal infection[111113] and respiratory syncytial virus [114, 115, 125].

Socioeconomic status also compared favourably against the Bradford Hill criteria, however the causal relationship is exerted through the influence of intermediary factors (e.g. crowding, income, education), which individually do not carry the same weight of evidence. A gradient of higher disease risk with lower socioeconomic status was demonstrated across ten studies.

Discussion

This systematic review identified 91 studies spanning 80 years that have assessed the relationship of social and environmental factors of crowding, dwelling characteristics and facilities, education, employment, income, nutrition and socioeconomic status with GAS infection, ARF, and RHD. Nearly all studies were observational rather than intervention studies. Crowding was the most frequently assessed factor followed by socioeconomic status. The majority of studies that assessed a measure of crowding and risk of GAS infection, ARF, or RHD reported a positive association with crowding; as did those examining dwelling characteristics, education levels and employment status of parents or cases, and nutrition. However, there was considerable heterogeneity in measures used, study settings and outcome ascertainment.

We noted a lack of well-designed research and interventions aimed at unravelling poverty as a mechanism for ARF and RHD, which is at odds with the widespread acceptance of ARF and RHD as diseases of poverty [2]. This paradox is exemplified in the hopeful remarks of Perry et al (1937)—the earliest study included in this review- that the noted association between crowding and ARF be ‘the starting-point and not the end of research…and that [further] research…may be fruitful in elucidating the aetiology of rheumatic heart disease and in discovering means for its prevention’; [96] yet 80 years later there remains a paucity of evidence of preventative actions at the primordial level.

This issue is well described among the neglected tropical diseases, [13, 122, 126, 127] a diverse group of communicable diseases that cause significant burden of suffering and economic impacts among poor and marginalised populations living in tropical and subtropical regions [128]. Poverty creates the milieu for these diseases to flourish; the low resource settings then exacerbate difficulties inherent in conducting high quality observational or interventional research. Finally, the neglect of the social, economic, political and physical contexts in which affected populations live, leaves the root causes unchanged [13, 122].

Given the study designs and limited quality of papers, we used the Bradford Hill criteria, a set of guiding principles for interpreting links between environmental influences and disease, as a pragmatic framework to consider the findings of this systematic review. These criteria are not definitive rules, rather they provide an analytical framework to consider whether cause and effect is the reasonable inference [129]. The weight of evidence in this systematic review supports a causative relationship between crowding and promotion of GAS transmission, and its rheumatic sequelae. Particular strengths were that evidence was collected across many study types including prospective and retrospective cohort studies and covered diverse population groups globally; features that enhance confidence in casual interpretation [129]. While the presence of a biological gradient may not rule out confounding (as a confounder may also exert a dose-response effect), it provides compelling evidence of a causative nature of this association. Furthermore, there is firm biologic plausibility, since GAS infection is transmitted by close contact and the respiratory route [130]. It can be inferred that crowding plays a critical mediating role between poverty and RHD prevalence, supported by those studies which included multivariable analyses [35, 40, 74, 90, 97, 105].

Overall socioeconomic status also effectively met the Bradford Hill criteria for causation of the outcomes of interest. Since this overarching category is collinear with (and either determined by or a determinant of) the other measures examined, it is not possible to tease out specifics relating to how each criterion was met. In general, it is well understood that rising socioeconomic status, prior to availability of penicillin, was associated with a steady decline in death rates from ARF in industrialised nations [131]. It is likely the combination of these adverse factors that creates the environment that drives ARF and RHD risk among socioeconomically disadvantaged populations. This compounding effect also explains why these factors individually do not necessarily exert the same risk.

The other factors explored in this review had insufficient evidence to suggest causal links. Dwelling characteristics frequently displayed an association with GAS infection, ARF, or RHD risk, but measures were so heterogeneous and context specific that generalizability is impossible. Further, authors consistently omitted a proposed mechanism to explain their findings. The role of fomites in GAS transmission was not supported [106, 108]. Soap and hand-washing had an impressive effect on reducing impetigo, but only one study explored this intervention [107]. Findings relating to education and employment were inconsistent. Specific nutritional interventions were suggested and tested, but lacked scale and consistency. Studies that demonstrated the association of low income and risk of GAS infection and associated diseases did not explore which economic deficits confer the risk (e.g. unaffordability of health care, poor diet etc.). General explorations of income as a social determinant of heath cite that low income exerts a risk to health through material deprivation (medical care, nutrition, housing, and sanitation) and social participation (education, employment) [120]. The association of income in this instance with RHD and its antecedents is likely a consequence of these intermediary factors.

Strengths and limitations

This systematic review is the most extensive review to date targeting observational and experimental studies in the area of social determinants of health and GAS infection, ARF and RHD. A limitation was the exclusion of non-English articles; nevertheless, a wide variety of countries were represented. A further limitation was that all stages of article appraisal were undertaken by one reviewer. However, a strict methodological process was followed utilising assessment tools designed for each study type allowing greater specificity in appraisal and uniformity in the reviewing process.

The poor quality of this body of evidence is the most critical limitation in guiding preventative actions; however, it would be erroneous to reject all findings. Rather it should be considered how probable or not it is that this diverse collection of studies dispersed in time, person and place could all be flawed and biased in the same way. Confounding is another important consideration in this review. Simple cause-effect relationships within social determinants of health are not readily apparent [13, 132]- rather they are complex and are characterized by multiple determinants, multiple outcomes, and multiple potential interactions [133]. That few included studies undertook multivariate analysis is a limitation of this review, which is why it was important to highlight their results explicitly in this analysis.

Many studies presented outcomes at a group or ecological level rather than an individual level. However, assessing social determinants of health at the group level is also important because people do not live in isolation; a population level approach ensures that a wide variety of contributing settings and activities are not inadvertently overlooked [134]. Also, these studies designs can reflect the interventions addressing the social determinants of health that are aimed at the population level.

Finally, reporting bias is an important consideration in systematic reviews. The factors extracted for this review were frequently not the primary outcome of studies, and so their positive, neutral or negative findings would be less likely to influence whether a paper was published.

Implications for ARF and RHD control

Rather than re-describe the problem, the aim of this research was to guide solutions. In ARF and RHD where treatment is logistically intensive and painful, [135] and vaccines or mass drug administration are not currently available options, the case for action on the social determinants that drive ARF and RHD risk is unquestionably convincing. Several candidate vaccines are in development, [136] but even if found to be safe and effective, not all at-risk populations would be able to readily access a new vaccine.

Based on these findings, we recommend that ARF and RHD control programs should address household crowding—particularly in high-income countries where funding and resourcing is more feasible. Structural crowding (inadequate living space including number of bedrooms) must be addressed in collaboration with designers and providers of public housing in partnerships that recognise housing needs to support good health.

Functional crowding (people sharing living spaces for safety, warmth or social cohesion, especially in traditional societies) is more difficult to address, requiring in-depth cultural understanding. For example, in Australian Aboriginal societies, rights and obligations around accommodating extra people in a house must be respected in interventions to reduce household crowding [137]. Where close living is important culturally, ways to live safely in larger households, focusing on ensuring adequate health literacy and washing facilities, need to be implemented.

Site-specific tailoring of interventions are needed: publically-funded interventions in a cold climate high RHD-burden setting for instance include the provision of household insulation and heating to reduce functional bedroom crowding [138]. Conversely, in hot climates, constructing community swimming pools is an effective intervention to decrease GAS skin infections, [139] though pools must be adequately managed so as to not introduce other health risks. Further practical interventions to mitigate the health risks arising from crowding include: community development projects to improve health literacy pertaining to infection transmission; creating community demand for sanitation and hygiene; [140] and effective community consultation about factors to motivate change in behaviour.

Interventions to tackle socioeconomic status may be considered beyond the reach of medical research and health service delivery, but this is not so. Research and service delivery initiatives in high RHD-burden settings should ensure that they provide opportunities for community engagement and employment; and funding bodies should ensure that initiatives supporting strengthening of socioeconomic status are valued as being critical in disease prevention.

RHD control programs, where they exist, should aim to routinely collect objective metrics on social and environmental factors to further inform advocacy, tailor it to local needs and add to the evidence base. Outcomes of advocacy should be interventions targeting social determinants such as crowding reduction and hygiene hardware improvement; and these should be accompanied by rigorous evaluation and sharing of findings.

Conclusion

Findings from this systematic review will be able to inform guidelines and policies regarding primordial-level preventative interventions against GAS infection, ARF and RHD. The wide body of evidence exploring links between certain social and environmental factors and these conditions is limited by poor quality and a lack of interventional studies. Historically, this has hampered the ability of control programs and guidelines to legitimately target these factors. However, when scrutinized against the Bradford Hill criteria assessing the evidence of a causal relationship, the link between overall socioeconomic status and crowding with ARF and RHD risk can be satisfactorily viewed as one of cause and effect. This clear and powerful message should be reflected in ARF and RHD control efforts. A critical role for ARF and RHD control programs and registers is to routinely collect and analyse data on these social determinants alongside clinical markers of case management to inform future advocacy and interventions.

Supporting information

S1 Checklist. PRISMA checklist.

(DOCX)

S1 Text. National Institute of health Study Quality Assessment Tool template.

(PDF)

S1 Fig. PRISMA flow diagram.

(TIF)

S1 Table. Search strategy.

(PDF)

S2 Table. Summary of crowding and GAS infection, ARF and RHD.

(DOCX)

S3 Table. Summary of dwelling characteristics and facilities and GAS infection, ARF and RHD.

(DOCX)

S4 Table. Summary of education and GAS infection, ARF and RHD.

(DOCX)

S5 Table. Summary of employment and GAS infection, ARF and RHD.

(DOCX)

S6 Table. Summary of income and GAS infection, ARF and RHD.

(DOCX)

S7 Table. Summary of nutrition and GAS infection, ARF and RHD.

(DOCX)

S8 Table. Summary of socioeconomic status and GAS infection, ARF and RHD.

(DOCX)

Data Availability

All relevant data are within the paper and its supporting information files.

Funding Statement

APR is supported by an Australian National Health and Medical Research Council fellowship (APP1113638). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.Ralph AP, Carapetis JR. Group a streptococcal diseases and their global burden. Current topics in microbiology and immunology. 2013;368:1–27. Epub 2012/12/18. doi: 10.1007/82_2012_280 . [DOI] [PubMed] [Google Scholar]
  • 2.Carapetis J, Steer A, Mulholland E. The Current Evidence for the Burden of Group A Streptococcal Diseases Geneva: World Health Organization, Development Department of Child and Adolescent Health and Development; 2005. [Google Scholar]
  • 3.Wyber R, Zuhlke L, Carapetis J. The case for global investment in rheumatic heart-disease control. Bulletin of the World Health Organization. 2014;92(10):768–70. doi: 10.2471/BLT.13.134486 ; PubMed Central PMCID: PMC4208481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.World Health Organization. Global Atlas on cardiovascular disease prevention and control. Geneva: 2011.
  • 5.McDonald M, Brown A, Edwards T, Hope A, Amu M, Morey F, et al. Apparent contrasting rates of pharyngitis and pyoderma in regions where rheumatic heart disease is highly prevalent. Heart, lung & circulation. 2007;16(4):254–9. Epub 2007/06/22. doi: 10.1016/j.hlc.2007.02.087 . [DOI] [PubMed] [Google Scholar]
  • 6.Remenyi B, Carapetis J, Wyber R, Taubert K, Mayosi BM, World Heart F. Position statement of the World Heart Federation on the prevention and control of rheumatic heart disease. Nature reviews Cardiology. 2013;10(5):284–92. Epub 2013/04/03. doi: 10.1038/nrcardio.2013.34 . [DOI] [PubMed] [Google Scholar]
  • 7.Centres for Disease Control. Group A Streptococcal Disease USA: CDC; 2016 [cited 2018 04/03/2018]. Available from: https://www.cdc.gov/groupastrep/diseases-hcp/strep-throat.html.
  • 8.Carapetis JR, Currie BJ, Mathews JD. Cumulative incidence of rheumatic fever in an endemic region: a guide to the susceptibility of the population? Epidemiology and infection. 2000;124(2):239–44. Epub 2000/05/17. ; PubMed Central PMCID: PMCPMC2810907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Gerber MA, Baltimore RS, Eaton CB, Gewitz M, Rowley AH, Shulman ST, et al. Prevention of rheumatic fever and diagnosis and treatment of acute Streptococcal pharyngitis: a scientific statement from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee of the Council on Cardiovascular Disease in the Young, the Interdisciplinary Council on Functional Genomics and Translational Biology, and the Interdisciplinary Council on Quality of Care and Outcomes Research: endorsed by the American Academy of Pediatrics. Circulation. 2009;119(11):1541–51. Epub 2009/02/28. doi: 10.1161/CIRCULATIONAHA.109.191959 . [DOI] [PubMed] [Google Scholar]
  • 10.Watkins D, Zuhlke L, Engel M, Daniels R, Francis V, Shaboodien G, et al. Seven key actions to eradicate rheumatic heart disease in Africa: the Addis Ababa communique. Cardiovascular journal of Africa. 2016;27(3):184–7. Epub 2016/01/28. doi: 10.5830/CVJA-2015-090 ; PubMed Central PMCID: PMCPMC5125265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Last J. A Dictionary of Public Health. UK: Oxford University Press; 2007. [Google Scholar]
  • 12.RHD Australia. About the disease- Rheumatic Heart Disease Darwin, Australia: RHD Australia Menzies School of Health Research; 2017. [cited 2017 03/07/2017]. Available from: https://www.rhdaustralia.org.au/about-disease. [Google Scholar]
  • 13.Allotey P, Reidpath DD, Pokhrel S. Social sciences research in neglected tropical diseases 1: the ongoing neglect in the neglected tropical diseases. Health research policy and systems. 2010;8:32 Epub 2010/10/22. doi: 10.1186/1478-4505-8-32 ; PubMed Central PMCID: PMCPmc2987896. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Yacoub M, Mayosi B, ElGuindy A, Carpentier A, Yusuf S. Eliminating acute rheumatic fever and rheumatic heart disease. Lancet (London, England). 2017;390(10091):212–3. doi: 10.1016/S0140-6736(17)31608-2 . [DOI] [PubMed] [Google Scholar]
  • 15.NIH. Study Quality Assessment Tools Bethesda, US: Natiional Institutes of Health; 2014. [cited 2016 03/08/2016]. Available from: https://www.nhlbi.nih.gov/health-pro/guidelines/in-develop/cardiovascular-risk-reduction/tools. [Google Scholar]
  • 16.Dufault B, Klar N. The quality of modern cross-sectional ecologic studies: a bibliometric review. American journal of epidemiology. 2011;174(10):1101–7. doi: 10.1093/aje/kwr241 . [DOI] [PubMed] [Google Scholar]
  • 17.Bradford Hill A. The Environment and Disease: Association of Causation? Proceedings of the Royal Society of Medicine. 1965;May(58):295–300. [PMC free article] [PubMed] [Google Scholar]
  • 18.Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Journal of clinical epidemiology. 2009;62(10):1006–12. doi: 10.1016/j.jclinepi.2009.06.005 . [DOI] [PubMed] [Google Scholar]
  • 19.Coburn AF. The concept of egg yolk as a dietary inhibitor to rheumatic susceptibility. Lancet (London, England). 1960;1(7129):867–70. Epub 1960/04/16. . [DOI] [PubMed] [Google Scholar]
  • 20.Holmes MC, Rubbo SD. A study of rheumatic fever and streptococcal infection in different social groups in Melbourne. The Journal of hygiene. 1953;51(4):450–7. Epub 1953/12/01. ; PubMed Central PMCID: PMCPmc2217775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.McDonald MI, Towers RJ, Andrews RM, Benger N, Currie BJ, Carapetis JR. Low rates of streptococcal pharyngitis and high rates of pyoderma in Australian aboriginal communities where acute rheumatic fever is hyperendemic. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America. 2006;43(6):683–9. Epub 2006/08/17. doi: 10.1086/506938 . [DOI] [PubMed] [Google Scholar]
  • 22.McDonald MJ, Towers RJ, Andrews R, Benger N, Fagan P, Currie BJ, et al. The dynamic nature of group A streptococcal epidemiology in tropical communities with high rates of rheumatic heart disease. Epidemiology and infection. 2008;136(4):529–39. doi: 10.1017/S0950268807008655 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Adanja B, Vlajinac H, Jarebinski M. Socioeconomic factors in the etiology of rheumatic fever. Journal of hygiene, epidemiology, microbiology, and immunology. 1988;32(3):329–35. Epub 1988/01/01. . [PubMed] [Google Scholar]
  • 24.Adanja BJ, Vlajinac HD, Marinkovic JP, Jarebinski MS. Rheumatic fever and diet. Israel journal of medical sciences. 1991;27(3):161–3. Epub 1991/03/01. . [PubMed] [Google Scholar]
  • 25.Vlajinac H, Adanja B, Jarebinski M. Socio-economic factors and rheumatic fever occurrence. Differences between patients with and without frequent sore throat. Journal of hygiene, epidemiology, microbiology, and immunology. 1989;33(4):471–6. Epub 1989/01/01. . [PubMed] [Google Scholar]
  • 26.Vlajinac H, Adanja B, Marinkovic J, Jarebinski M. Influence of socio-economic and other factors on rheumatic fever occurrence. Eur J Epidemiol. 1991;7(6):702–4. . [DOI] [PubMed] [Google Scholar]
  • 27.Zaman MM, Yoshiike N, Chowdhury AH, Nakayama T, Yokoyama T, Faruque GM, et al. Nutritional factors associated with rheumatic fever. Journal of tropical pediatrics. 1998;44(3):142–7. Epub 1998/07/29. doi: 10.1093/tropej/44.3.142 . [DOI] [PubMed] [Google Scholar]
  • 28.Zaman MM, Yoshiike N, Rouf MA, Haque S, Chowdhury AH, Nakayama T, et al. Association of rheumatic fever with serum albumin concentration and body iron stores in Bangladeshi children: case-control study. BMJ (Clinical research ed). 1998;317(7168):1287–8. Epub 1998/11/07. ; PubMed Central PMCID: PMCPmc28708. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Kerdemelidis M, Lennon DR, Arroll B, Peat B, Jarman J. The primary prevention of rheumatic fever. Journal of paediatrics and child health. 2010;46(9):534–48. Epub 2010/09/22. doi: 10.1111/j.1440-1754.2010.01854.x . [DOI] [PubMed] [Google Scholar]
  • 30.Steer AC, Carapetis JR, Nolan TM, Shann F. Systematic review of rheumatic heart disease prevalence in children in developing countries: the role of environmental factors. Journal of paediatrics and child health. 2002;38(3):229–34. Epub 2002/06/06. . [DOI] [PubMed] [Google Scholar]
  • 31.Rothenbuhler M, O'Sullivan CJ, Stortecky S, Stefanini GG, Spitzer E, Estill J, et al. Active surveillance for rheumatic heart disease in endemic regions: a systematic review and meta-analysis of prevalence among children and adolescents. The Lancet Global health. 2014;2(12):e717–26. Epub 2014/12/01. doi: 10.1016/S2214-109X(14)70310-9 . [DOI] [PubMed] [Google Scholar]
  • 32.Grave PE. Social and environmental factors in the aetiology of rheumatic fever. The Medical journal of Australia. 1957;44(18):602–8. Epub 1957/05/04. . [DOI] [PubMed] [Google Scholar]
  • 33.Dobson J, Steer AC, Colquhoun S, Kado J. Environmental factors and rheumatic heart disease in Fiji. Pediatric cardiology. 2012;33(2):332–6. Epub 2011/11/08. doi: 10.1007/s00246-011-0139-x . [DOI] [PubMed] [Google Scholar]
  • 34.Gray FG, Quinn RW, Quinn JP. A long-term survey of rheumatic and non-rheumatic families; with particular reference to environment and heredity. The American journal of medicine. 1952;13(4):400–12. . [DOI] [PubMed] [Google Scholar]
  • 35.Riaz BK, Selim S, Karim MN, Chowdhury KN, Chowdhury SH, Rahman MR. Risk factors of rheumatic heart disease in Bangladesh: a case-control study. Journal of health, population, and nutrition. 2013;31(1):70–7. Epub 2013/04/27. ; PubMed Central PMCID: PMCPmc3702361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Zaman MM, Yoshiike N, Chowdhury AH, Jalil MQ, Mahmud RS, Faruque GM, et al. Socio-economic deprivation associated with acute rheumatic fever. A hospital-based case-control study in Bangladesh. Paediatric and perinatal epidemiology. 1997;11(3):322–32. Epub 1997/07/01. . [DOI] [PubMed] [Google Scholar]
  • 37.Kurahara DK, Grandinetti A, Galario J, Reddy DV, Tokuda A, Langan S, et al. Ethnic differences for developing rheumatic fever in a low-income group living in Hawaii. Ethnicity & disease. 2006;16(2):357–61. Epub 2007/01/04. ; PubMed Central PMCID: PMCPmc1643848. [PMC free article] [PubMed] [Google Scholar]
  • 38.Levine JI, Chapman SS, Guerra V, Cooper J, Krause RM. Studies on the transmission within families of Group A hemolytic streptococci. J Lab Clin Med. 1966;67(3):483–94. . [PubMed] [Google Scholar]
  • 39.Wilcox EB, Galloway LS. Children with and without rheumatic fever. I. Nutrient intake, physique, and growth. Journal of the American Dietetic Association. 1954;30(4):345–50. Epub 1954/04/01. . [PubMed] [Google Scholar]
  • 40.Okello E, Kakande B, Sebatta E, Kayima J, Kuteesa M, Mutatina B, et al. Socioeconomic and environmental risk factors among rheumatic heart disease patients in Uganda. PloS one. 2012;7(8):e43917 Epub 2012/09/07. doi: 10.1371/journal.pone.0043917 ; PubMed Central PMCID: PMCPmc3428272. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Hewitt D, Stewart A. Some epidemiological aspects of acute rheumatism. British journal of social medicine. 1952;6(3):161–8. Epub 1952/07/01. ; PubMed Central PMCID: PMCPmc1037311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Bach JF, Chalons S, Forier E, Elana G, Jouanelle J, Kayemba S, et al. 10-year educational programme aimed at rheumatic fever in two French Caribbean islands. Lancet (London, England). 1996;347(9002):644–8. Epub 1996/03/09. . [DOI] [PubMed] [Google Scholar]
  • 43.Brownell KD, Bailen-Rose F. Acute rheumatic fever in children. Incidence in a borough of New York City. Jama. 1973;224(12):1593–7. Epub 1973/06/18. . [PubMed] [Google Scholar]
  • 44.Diamond EF. Hereditary and environmental factors in the pathogenesis of rheumatic fever. Pediatrics. 1957;19(5):908–15. Epub 1957/05/01. . [PubMed] [Google Scholar]
  • 45.Lennon D, Martin D, Wong E, Taylor LR. Longitudinal study of poststreptococcal disease in Auckland; rheumatic fever, glomerulonephritis, epidemiology and M typing 1981–86. The New Zealand medical journal. 1988;101(847 Pt 2):396–8. . [PubMed] [Google Scholar]
  • 46.Meira ZM, Goulart EM, Colosimo EA, Mota CC. Long term follow up of rheumatic fever and predictors of severe rheumatic valvar disease in Brazilian children and adolescents. Heart (British Cardiac Society). 2005;91(8):1019–22. Epub 2005/07/16. doi: 10.1136/hrt.2004.042762 ; PubMed Central PMCID: PMCPmc1769032. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Potter EV, Svartman M, Poon-King T, Earle DP. The families of patients with acute rheumatic fever or glomerulonephritis in Trinidad. American journal of epidemiology. 1977;106(2):130–8. . [DOI] [PubMed] [Google Scholar]
  • 48.Veasy LG, Tani LY, Hill HR. Persistence of acute rheumatic fever in the intermountain area of the United States. The Journal of pediatrics. 1994;124(1):9–16. . [DOI] [PubMed] [Google Scholar]
  • 49.Westlake RM, Graham TP, Edwards KM. An outbreak of acute rheumatic fever in Tennessee. The Pediatric infectious disease journal. 1990;9(2):97–100. Epub 1990/02/01. . [DOI] [PubMed] [Google Scholar]
  • 50.Wannamaker L. Chapter 12: The epidemiology of streptococcal infections In: McCarthy M, editor. Streptococcal infections. New York: Columbia University Press; 1954. p. 157–75. [Google Scholar]
  • 51.McDonald MI, Towers RJ, Andrews R, Benger N, Fagan P, Currie BJ, et al. The dynamic nature of group A streptococcal epidemiology in tropical communities with high rates of rheumatic heart disease. Epidemiology and infection. 2008;136(4):529–39. Epub 2007/06/02. doi: 10.1017/S0950268807008655 ; PubMed Central PMCID: PMCPmc2870827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Breese BB, Disney FA. The successful treatment of beta hemolytic streptococcal infections in children with a single injection of repository penicillin (benzathine penicillin G). Pediatrics. 1955;15(5):516–21. . [PubMed] [Google Scholar]
  • 53.Coggon D, Barker DJ, Inskip H, Wield G. Housing in early life and later mortality. Journal of epidemiology and community health. 1993;47(5):345–8. Epub 1993/10/01. ; PubMed Central PMCID: PMCPmc1059825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Eriksson JG, Kajantie E, Phillips DI, Osmond C, Thornburg KL, Barker DJ. The developmental origins of chronic rheumatic heart disease. American journal of human biology: the official journal of the Human Biology Council. 2013;25(5):655–8. Epub 2013/08/06. doi: 10.1002/ajhb.22425 . [DOI] [PubMed] [Google Scholar]
  • 55.Jackson RL, Kelly HG, et al. Rheumatic fever recurrences in children without sulfonamide prophylaxis; an evaluation of environmental factors. The Journal of pediatrics. 1947;31(4):390–402. Epub 1947/10/01. . [DOI] [PubMed] [Google Scholar]
  • 56.Mirabel M, Fauchier T, Bacquelin R, Tafflet M, Germain A, Robillard C, et al. Echocardiography screening to detect rheumatic heart disease: A cohort study of schoolchildren in French Pacific Islands. International journal of cardiology. 2015;188:89–95. Epub 2015/04/19. doi: 10.1016/j.ijcard.2015.04.007 . [DOI] [PubMed] [Google Scholar]
  • 57.Nandi S, Kumar R, Ray P, Vohra H, Ganguly NK. Group A streptococcal sore throat in a periurban population of northern India: a one-year prospective study. Bulletin of the World Health Organization. 2001;79(6):528–33. Epub 2001/07/05. ; PubMed Central PMCID: PMCPmc2566441. [PMC free article] [PubMed] [Google Scholar]
  • 58.Quinn RW, Lowry PN, Zwaag RV. Significance of hemolytic streptococci for Nashville school children: clinical and serologic observations. Southern medical journal. 1978;71(3):242–6. Epub 1978/03/01. . [DOI] [PubMed] [Google Scholar]
  • 59.Ransome OJ, Roode H, Spector I, Reinach SG. Pharyngeal carriage of group A beta-haemolytic streptococci in coloured and Indian schoolchildren. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde. 1983;64(20):779–81. . [PubMed] [Google Scholar]
  • 60.Tay L, Chay SO. A three-year streptococcal survey among Singapore school children. Part I—Carriership of streptococci. Annals of the Academy of Medicine, Singapore. 1981;10(1):14–24. Epub 1981/01/01. . [PubMed] [Google Scholar]
  • 61.Westerling R, Gullberg A, Rosen M. Socioeconomic differences in 'avoidable' mortality in Sweden 1986–1990. International journal of epidemiology. 1996;25(3):560–7. Epub 1996/06/01. . [DOI] [PubMed] [Google Scholar]
  • 62.Bernstein SH. Observations on the effects of housing on the incidence and spread of common respiratory diseases among Air Force recruits. Am J Hyg. 1957;65(2):162–71. . [DOI] [PubMed] [Google Scholar]
  • 63.Agarwal AK, Yunus M, Ahmad J, Khan A. Rheumatic heart disease in India. Journal of the Royal Society of Health. 1995;115(5):303–4, 9. Epub 1995/10/01. . [DOI] [PubMed] [Google Scholar]
  • 64.Ba-Saddik IA, Munibari AA, Al-Naqeeb MS, Parry CM, Hart CA, Cuevas LE, et al. Prevalence of rheumatic heart disease among school-children in Aden, Yemen. Annals of tropical paediatrics. 2011;31(1):37–46. Epub 2011/01/26. doi: 10.1179/1465328110Y.0000000007 . [DOI] [PubMed] [Google Scholar]
  • 65.Bassili A, Zaher SR, Zaki A, Abdel-Fattah M, Tognoni G. Profile of secondary prophylaxis among children with rheumatic heart disease in Alexandria, Egypt. Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit. 2000;6(2–3):437–46. Epub 2001/09/15. . [PubMed] [Google Scholar]
  • 66.Beaton A, Lu JC, Aliku T, Dean P, Gaur L, Weinberg J, et al. The utility of handheld echocardiography for early rheumatic heart disease diagnosis: a field study. Eur Heart J Cardiovasc Imaging. 2015;16(5):475–82. Epub 2015/01/08. doi: 10.1093/ehjci/jeu296 ; PubMed Central PMCID: PMCPmc4542771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Bhave SY, Kinikar A, Sane S, Agarwal M, Amdekar YK. Epidemiology of streptococcal infection with reference to rheumatic fever. Indian pediatrics. 1991;28(12):1503–8. Epub 1991/12/01. . [PubMed] [Google Scholar]
  • 68.Chaikitpinyo A, Panamonta M, Wongswadiwat Y, Weraarchakul W, Panamonta O, Panthongviriyakul A, et al. Rheumatic and congenital heart diseases among school children of Khon Kaen, Thailand: Declining prevalence of rheumatic heart disease. Asian Biomedicine. 2014;8(5):645–50. [Google Scholar]
  • 69.Faruq QO, Rashid AK, Ahmed J, Waiz A, Haque KM, Rouf MA, et al. Prevalence of streptococcal sorethroat in the school children of Dhaka. Bangladesh Medical Research Council bulletin. 1995;21(3):87–94. Epub 1995/12/01. . [PubMed] [Google Scholar]
  • 70.Hammon WM, Sather GE, Hollinger N. Preliminary report of epidemiological studies on poliomyelitis and streptococcal infections; Lansing neutralizing antibody and antistreptolysin O surveys of California cities, Texas, North Carolina, Mexico, Pacific Islands, and Japan. American journal of public health and the nation's health. 1950;40(3):293–306. ; PubMed Central PMCID: PMCPMC1528413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Imamoglu A, Ozen S. Epidemiology of rheumatic heart disease. Archives of disease in childhood. 1988;63(12):1501–3. Epub 1988/12/01. ; PubMed Central PMCID: PMCPmc1779215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Ledos PH, Kamblock J, Bourgoin P, Eono P, Carapetis JR. Prevalence of rheumatic heart disease in young adults from New Caledonia. Archives of cardiovascular diseases. 2015;108(1):16–22. Epub 2014/12/17. doi: 10.1016/j.acvd.2014.07.053 . [DOI] [PubMed] [Google Scholar]
  • 73.Likitnukul S, Prapphal N, Tatiyakavee K, Nunthapisud P, Chumdermpadetsuk S. Risk factors of streptococcal colonization in school age children. The Southeast Asian journal of tropical medicine and public health. 1994;25(4):664–71. Epub 1994/12/01. . [PubMed] [Google Scholar]
  • 74.Longo-Mbenza B, Bayekula M, Ngiyulu R, Kintoki VE, Bikangi NF, Seghers KV, et al. Survey of rheumatic heart disease in school children of Kinshasa town. International journal of cardiology. 1998;63(3):287–94. Epub 1998/05/13. . [DOI] [PubMed] [Google Scholar]
  • 75.Lumsden RH, Akwanalo C, Chepkwony S, Kithei A, Omollo V, Holland TL, et al. Clinical and geographic patterns of rheumatic heart disease in outpatients attending cardiology clinic in western Kenya. International journal of cardiology. 2016;223:228–35. doi: 10.1016/j.ijcard.2016.08.069 [DOI] [PubMed] [Google Scholar]
  • 76.McLaren MJ, Hawkins DM, Koornhof HJ, Bloom KR, Bramwell-Jones DM, Cohen E, et al. Epidemiology of rheumatic heart disease in black shcoolchildren of Soweto, Johannesburg. British medical journal. 1975;3(5981):474–8. Epub 1975/08/23. ; PubMed Central PMCID: PMCPmc1674319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Periwal KL, Gupta BK, Panwar RB, Khatri PC, Raja S, Gupta R. Prevalence of rheumatic heart disease in school children in Bikaner: an echocardiographic study. The Journal of the Association of Physicians of India. 2006;54:279–82. Epub 2006/09/02. . [PubMed] [Google Scholar]
  • 78.Piper GW. Rural housing and rheumatic fever. Can J Public Health. 1970;61(2):122–5. Epub 1970/03/01. . [PubMed] [Google Scholar]
  • 79.Poppi A, Labo G, Lenzi G, Rosa L. Epidemiology of rheumatic fever in a rural district in Italy, with particular reference to some environmental factors. Annals of the rheumatic diseases. 1953;12(4):310–4. Epub 1953/12/01. ; PubMed Central PMCID: PMCPmc1030541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Quinn RW, Watkins JH, Quinn JP. Rheumatic heart disease and crowding; a survey of rural and urban Connecticut school children. American journal of public health and the nation's health. 1948;38(8):1071–81. Epub 1948/08/01. ; PubMed Central PMCID: PMCPmc1624530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Quinn RW, Liao SJ, Quinn JP. An environmental and sociological study of rheumatic heart disease. American journal of public health and the nation's health. 1950;40(10):1285–95. Epub 1950/10/01. ; PubMed Central PMCID: PMCPmc1528844. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Rizvi SF, Khan MA, Kundi A, Marsh DR, Samad A, Pasha O. Status of rheumatic heart disease in rural Pakistan. Heart (British Cardiac Society). 2004;90(4):394–9. doi: 10.1136/hrt.2003.025981 ; PubMed Central PMCID: PMCPMC1768176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Rushdy AA, Cooke RP, Iversen AM, Pickering BJ. Boarding school outbreak of group A streptococcal pharyngitis. Communicable disease report CDR review. 1995;5(7):R106–8. Epub 1995/06/23. . [PubMed] [Google Scholar]
  • 84.Saxena A, Ramakrishnan S, Roy A, Seth S, Krishnan A, Misra P, et al. Prevalence and outcome of subclinical rheumatic heart disease in India: the RHEUMATIC (Rheumatic Heart Echo Utilisation and Monitoring Actuarial Trends in Indian Children) study. Heart (British Cardiac Society). 2011;97(24):2018–22. Epub 2011/11/15. doi: 10.1136/heartjnl-2011-300792 . [DOI] [PubMed] [Google Scholar]
  • 85.Spitzer J, Hennessy E, Neville L. High group A streptococcal carriage in the Orthodox Jewish community of north Hackney. The British journal of general practice: the journal of the Royal College of General Practitioners. 2001;51(463):101–5. Epub 2001/02/24. ; PubMed Central PMCID: PMCPmc1313922. [PMC free article] [PubMed] [Google Scholar]
  • 86.Steer AC, Kado J, Wilson N, Tuiketei T, Batzloff M, Waqatakirewa L, et al. High prevalence of rheumatic heart disease by clinical and echocardiographic screening among children in Fiji. The Journal of heart valve disease. 2009;18(3):327–35; discussion 36. Epub 2009/06/30. . [PubMed] [Google Scholar]
  • 87.Thakur JS, Negi PC, Ahluwalia SK, Vaidya NK. Epidemiological survey of rheumatic heart disease among school children in the Shimla Hills of northern India: prevalence and risk factors. Journal of epidemiology and community health. 1996;50(1):62–7. Epub 1996/02/01. ; PubMed Central PMCID: PMCPmc1060206. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 88.Vashistha VM, Kalra A, Kalra K, Jain VK. Prevalence of rheumatic heart disease in school children. Indian pediatrics. 1993;30(1):53–6. Epub 1993/01/01. . [PubMed] [Google Scholar]
  • 89.Yazov L, Petros WG, Stump E. Epidemiological studies on rheumatic heart disease and streptococcal carriers among school-children in Addis-Ababa, Ethiopia. Preliminary communication. Zeitschrift fur Rheumatologie. 1978;37(9–10):304–8. Epub 1978/09/01. . [PubMed] [Google Scholar]
  • 90.Jaine R, Baker M, Venugopal K. Acute rheumatic fever associated with household crowding in a developed country. The Pediatric infectious disease journal. 2011;30(4):315–9. Epub 2010/10/16. doi: 10.1097/INF.0b013e3181fbd85b . [DOI] [PubMed] [Google Scholar]
  • 91.Krause RM. The influence of infection on the geography of heart disease. Circulation. 1979;60(5):972–6. Epub 1979/11/01. . [DOI] [PubMed] [Google Scholar]
  • 92.Milne RJ, Lennon DR, Stewart JM, Vander Hoorn S, Scuffham PA. Incidence of acute rheumatic fever in New Zealand children and youth. Journal of paediatrics and child health. 2012;48(8):685–91. Epub 2012/04/13. doi: 10.1111/j.1440-1754.2012.02447.x . [DOI] [PubMed] [Google Scholar]
  • 93.Morton WE, Lichty JA. Rheumatic heart disease epidemiology. II. Colorado's high-risk low-socioeconomic region in 1960. American journal of epidemiology. 1970;92(2):113–20. Epub 1970/08/01. . [DOI] [PubMed] [Google Scholar]
  • 94.Odio A. The incidence of acute rheumatic fever in a suburban area of Los Angeles. A ten-year study. The Western journal of medicine. 1986;144(2):179–84. Epub 1986/02/01. ; PubMed Central PMCID: PMCPmc1306555. [PMC free article] [PubMed] [Google Scholar]
  • 95.Pennock V, Bell A, Moxon TA, Reed P, Maxwell F, Lennon D. Retrospective epidemiology of acute rheumatic fever: a 10-year review in the Waikato District Health Board area of New Zealand. The New Zealand medical journal. 2014;127(1393):26–37. Epub 2014/05/13. . [PubMed] [Google Scholar]
  • 96.Perry B, Roberts F. A study on the variability in the incidence of rheumatic heart disease within the city of Bristol. Rheumatic Health Disease in Bristol. 1937;Supplment:154–8. [Google Scholar]
  • 97.Phillips DIW, Osmond C. Is susceptibility to chronic rheumatic heart disease determined in early infancy? An analysis of mortality in Britain during the 20th century. Global Cardiology Science and Practice. 2014;2014(4). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 98.Quinn RW, Quinn JP. Mortality due to rheumatic heart disease in the socioeconomic districts of New Haven, Connecticut. The Yale journal of biology and medicine. 1951;24(1):15–21. Epub 1951/09/01. ; PubMed Central PMCID: PMCPmc2599086. [PMC free article] [PubMed] [Google Scholar]
  • 99.Quinn RW. Hemolytic streptococci in Nashville school children. Southern medical journal. 1980;73(3):288–96. Epub 1980/03/01. . [DOI] [PubMed] [Google Scholar]
  • 100.Roberts KV, Maguire GP, Brown A, Atkinson DN, Remenyi B, Wheaton G, et al. Rheumatic heart disease in Indigenous children in northern Australia: differences in prevalence and the challenges of screening. The Medical journal of Australia. 2015;203(5):221.e1–7. Epub 2016/02/08. . [DOI] [PubMed] [Google Scholar]
  • 101.Robin A, Mills C, Tuck R, Lennon D. The epidemiology of acute rheumatic fever in Northland, 2002–2011. The New Zealand medical journal. 2013;126(1373):46–52. Epub 2013/06/26. . [PubMed] [Google Scholar]
  • 102.Rosati G, Granieri E, Pinna L, Aiello I, De Bastiani P, Tola R. The geographical distribution of multiple sclerosis, rheumatoid arthritis, rheumatic heart disease and poststreptococcal nephritis in Sardinia: climatic and socioeconomic factors. Journal of neurology. 1978;219(1):27–35. Epub 1978/09/12. [DOI] [PubMed] [Google Scholar]
  • 103.Siriett V, Crengle S, Lennon D, Stonehouse M, Cramp G. The epidemiology of rheumatic fever in the Tairawhiti/Gisborne region of New Zealand: 1997–2009. The New Zealand medical journal. 2012;125(1365):8–15. Epub 2012/12/21. . [PubMed] [Google Scholar]
  • 104.Smith MT, Lester-Smith D, Zurynski Y, Noonan S, Carapetis JR, Elliott EJ. Persistence of acute rheumatic fever in a tertiary children's hospital. Journal of paediatrics and child health. 2011;47(4):198–203. Epub 2011/01/05. doi: 10.1111/j.1440-1754.2010.01935.x . [DOI] [PubMed] [Google Scholar]
  • 105.Wedum AG, Wedum BG. Rheumatic Fever in Cincinnati in Relation to Rentals, Crowding, Density of Population, and Negroes. American journal of public health and the nation's health. 1944;34(10):1065–70. Epub 1944/10/01. ; PubMed Central PMCID: PMCPmc1625273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Falck G, Kjellander J, Schwan A. Recurrence rate of streptococcal pharyngitis related to hygienic measures. Scandinavian journal of primary health care. 1998;16(1):8–12. Epub 1998/06/05. . [DOI] [PubMed] [Google Scholar]
  • 107.Luby SP, Agboatwalla M, Feikin DR, Painter J, Billhimer W, Altaf A, et al. Effect of handwashing on child health: a randomised controlled trial. Lancet (London, England). 2005;366(9481):225–33. Epub 2005/07/19. doi: 10.1016/S0140-6736(05)66912-7 . [DOI] [PubMed] [Google Scholar]
  • 108.Perry W, Siegel A, Rammelkamp C, Wannamaker L. Transmission of Group A Streptococci I. The Role of Contaminated Bedding. American Journal of Hygiene. 1957;66:85–95. [DOI] [PubMed] [Google Scholar]
  • 109.Gordis L, Lilienfeld A, Rodriguez R. Studies in the epidemiology and preventability of rheumatic fever. II. Socio-economic factors and the incidence of acute attacks. Journal of chronic diseases. 1969;21(9):655–66. Epub 1969/02/01. . [DOI] [PubMed] [Google Scholar]
  • 110.Beaton A, Okello E, Lwabi P, Mondo C, McCarter R, Sable C. Echocardiography screening for rheumatic heart disease in Ugandan schoolchildren. Circulation. 2012;125(25):3127–32. Epub 2012/05/26. doi: 10.1161/CIRCULATIONAHA.112.092312 . [DOI] [PubMed] [Google Scholar]
  • 111.Yezli S, Assiri AM, Alhakeem RF, Turkistani AM, Alotaibi B. Meningococcal disease during the Hajj and Umrah mass gatherings. International journal of infectious diseases: IJID: official publication of the International Society for Infectious Diseases. 2016;47:60–4. Epub 2016/04/12. doi: 10.1016/j.ijid.2016.04.007 . [DOI] [PubMed] [Google Scholar]
  • 112.Deutch S, Labouriau R, Schonheyeder HC, Ostergaard L, Norgard B, Sorensen HT. Crowding as a risk factor of meningococcal disease in Danish preschool children: a nationwide population-based case-control study. Scand J Infect Dis. 2004;36(1):20–3. Epub 2004/03/06. . [DOI] [PubMed] [Google Scholar]
  • 113.Baker M, McNicholas A, Garrett N, Jones N, Stewart J, Koberstein V, et al. Household crowding a major risk factor for epidemic meningococcal disease in Auckland children. The Pediatric infectious disease journal. 2000;19(10):983–90. Epub 2000/10/31. . [DOI] [PubMed] [Google Scholar]
  • 114.Bont L, Checchia PA, Fauroux B, Figueras-Aloy J, Manzoni P, Paes B, et al. Defining the Epidemiology and Burden of Severe Respiratory Syncytial Virus Infection Among Infants and Children in Western Countries. Infectious diseases and therapy. 2016;5(3):271–98. Epub 2016/08/03. doi: 10.1007/s40121-016-0123-0 ; PubMed Central PMCID: PMCPmc5019979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Colosia AD, Masaquel A, Hall CB, Barrett AM, Mahadevia PJ, Yogev R. Residential crowding and severe respiratory syncytial virus disease among infants and young children: a systematic literature review. BMC Infect Dis. 2012;12:95 Epub 2012/04/24. doi: 10.1186/1471-2334-12-95 ; PubMed Central PMCID: PMCPmc3405464. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Shi T, Balsells E, Wastnedge E, Singleton R, Rasmussen ZA, Zar HJ, et al. Risk factors for respiratory syncytial virus associated with acute lower respiratory infection in children under five years: Systematic review and meta-analysis. Journal of global health. 2015;5(2):020416 Epub 2015/12/19. doi: 10.7189/jogh.05.020416 ; PubMed Central PMCID: PMCPmc4676580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 117.Thomson H, Thomas S, Sellstrom E, Petticrew M. Housing improvements for health and associated socio-economic outcomes. The Cochrane database of systematic reviews. 2013;(2):CD008657 doi: 10.1002/14651858.CD008657.pub2 . [DOI] [PubMed] [Google Scholar]
  • 118.Stallings R. Child Morbidity and Treatment Patterns. Calverton, Maryland: 2004.
  • 119.van Rossum CT, Shipley MJ, van de Mheen H, Grobbee DE, Marmot MG. Employment grade differences in cause specific mortality. A 25 year follow up of civil servants from the first Whitehall study. Journal of epidemiology and community health. 2000;54(3):178–84. Epub 2000/04/04. doi: 10.1136/jech.54.3.178 ; PubMed Central PMCID: PMCPMC1731642. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 120.Marmot M. The influence of income on health: views of an epidemiologist. Health affairs. 2002;21(2):31–46. . [DOI] [PubMed] [Google Scholar]
  • 121.Laupland KB, Davies HD, Low DE, Schwartz B, Green K, McGeer A. Invasive group A streptococcal disease in children and association with varicella-zoster virus infection. Ontario Group A Streptococcal Study Group. Pediatrics. 2000;105(5):E60 Epub 2000/05/09. . [DOI] [PubMed] [Google Scholar]
  • 122.Houweling TA, Karim-Kos HE, Kulik MC, Stolk WA, Haagsma JA, Lenk EJ, et al. Socioeconomic Inequalities in Neglected Tropical Diseases: A Systematic Review. PLoS Negl Trop Dis. 2016;10(5):e0004546 Epub 2016/05/14. doi: 10.1371/journal.pntd.0004546 ; PubMed Central PMCID: PMCPMC4865383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 123.Carapetis JR, Walker AM, Hibble M, Sriprakash KS, Currie BJ. Clinical and epidemiological features of group A streptococcal bacteraemia in a region with hyperendemic superficial streptococcal infection. Epidemiology and infection. 1999;122(1):59–65. Epub 1999/03/31. ; PubMed Central PMCID: PMCPmc2809588. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.World Health Organization. What are the health risks related to overcrowding? Geneva: World Health Organization; 2017. [cited 2017 20/06/2017]. Available from: http://www.who.int/water_sanitation_health/emergencies/qa/emergencies_qa9/en/. [Google Scholar]
  • 125.Asker M, Asker S. Sleep Apnea in Patients with Rheumatic Mitral Stenosis. The Journal of heart valve disease. 2015;24(3):325–30. Epub 2016/02/24. . [PubMed] [Google Scholar]
  • 126.Kappagoda S, Ioannidis JP. Neglected tropical diseases: survey and geometry of randomised evidence. BMJ (Clinical research ed). 2012;345:e6512 Epub 2012/10/24. doi: 10.1136/bmj.e6512 ; PubMed Central PMCID: PMCPmc3478233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127.Hotez PJ, Alvarado M, Basanez MG, Bolliger I, Bourne R, Boussinesq M, et al. The global burden of disease study 2010: interpretation and implications for the neglected tropical diseases. PLoS Negl Trop Dis. 2014;8(7):e2865 Epub 2014/07/25. doi: 10.1371/journal.pntd.0002865 ; PubMed Central PMCID: PMCPmc4109880. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 128.World Health Organization. Neglected Tropical Diseases Switzerland: World Health Organization; 2018 [cited 2018 04/03/2018]. Available from: http://www.who.int/neglected_diseases/diseases/en/.
  • 129.Lucas R, McMichael A. Association or causation: evaluation links between “environmental and disease”. Bulletin of the World Health Organization. 2005;83(10):792–5. [PMC free article] [PubMed] [Google Scholar]
  • 130.Carapetis JR, Currie BJ, Kaplan EL. Epidemiology and prevention of group A streptococcal infections: acute respiratory tract infections, skin infections, and their sequelae at the close of the twentieth century. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America. 1999;28(2):205–10. doi: 10.1086/515114 . [DOI] [PubMed] [Google Scholar]
  • 131.Gordis L. The virtual disappearance of rheumatic fever in the United States: lessons in the rise and fall of disease. T. Duckett Jones memorial lecture. Circulation. 1985;72(6):1155–62. . [DOI] [PubMed] [Google Scholar]
  • 132.Bonnefoy J, Morgan A, Kelly MP, Butt J, Bergman V. Constructing the evidence base on the social determinants of health: A guide London: Measurement and Evidence Knowledge Network of the WHO Commission on Social Determinants of Health; 2007. [Google Scholar]
  • 133.McQueen DV. Three challenges for the social determinants of health pursuit. Int J Public Health. 2009;54(1):1–2. Epub 2009/02/05. doi: 10.1007/s00038-008-8167-x . [DOI] [PubMed] [Google Scholar]
  • 134.Song R, Hall HI, Harrison KM, Sharpe TT, Lin LS, Dean HD. Identifying the impact of social determinants of health on disease rates using correlation analysis of area-based summary information. Public health reports (Washington, DC: 1974). 2011;126 Suppl 3:70–80. Epub 2011/08/13. doi: 10.1177/00333549111260s312 ; PubMed Central PMCID: PMCPMC3150132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135.Ralph AP, Fittock M, Schultz R, Thompson D, Dowden M, Clemens T, et al. Improvement in rheumatic fever and rheumatic heart disease management and prevention using a health centre-based continuous quality improvement approach. BMC health services research. 2013;13:525 Epub 2013/12/20. doi: 10.1186/1472-6963-13-525 ; PubMed Central PMCID: PMCPmc3878366. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 136.Pandey M, Powell J, Calcutt A, Zaman M , Phillips ZN, Ho MF et al. Physicochemical characterisation, immunogenicity and protective efficacy of a lead streptococcal vaccine: progress towards Phase I trial. Sci Rep. 2017. October 23;7(1):13786 doi: 10.1038/s41598-017-14157-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 137.Memmott P, Birdsall-Jones C, Greenop K. Australian Indigenous house crowding, AHURI Final Report No. 194. Melbourne: 2012.
  • 138.Minister of Health. Implementing the New Zealand Health Strategy 2013. Wellington: 2013.
  • 139.Hendrickx D, Stephen A, Lehmann D, Silva D, Boelaert M, Carapetis J, et al. A systematic review of the evidence that swimming pools improve health and wellbeing in remote Aboriginal communities in Australia. Australian and New Zealand journal of public health. 2016;40(1):30–6. doi: 10.1111/1753-6405.12433 . [DOI] [PubMed] [Google Scholar]
  • 140.Waterkeyn J, Cairncross S. Creating demand for sanitation and hygiene through Community Health Clubs: a cost-effective intervention in two districts in Zimbabwe. Social science & medicine (1982). 2005;61(9):1958–70. doi: 10.1016/j.socscimed.2005.04.012 . [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

S1 Checklist. PRISMA checklist.

(DOCX)

S1 Text. National Institute of health Study Quality Assessment Tool template.

(PDF)

S1 Fig. PRISMA flow diagram.

(TIF)

S1 Table. Search strategy.

(PDF)

S2 Table. Summary of crowding and GAS infection, ARF and RHD.

(DOCX)

S3 Table. Summary of dwelling characteristics and facilities and GAS infection, ARF and RHD.

(DOCX)

S4 Table. Summary of education and GAS infection, ARF and RHD.

(DOCX)

S5 Table. Summary of employment and GAS infection, ARF and RHD.

(DOCX)

S6 Table. Summary of income and GAS infection, ARF and RHD.

(DOCX)

S7 Table. Summary of nutrition and GAS infection, ARF and RHD.

(DOCX)

S8 Table. Summary of socioeconomic status and GAS infection, ARF and RHD.

(DOCX)

Data Availability Statement

All relevant data are within the paper and its supporting information files.


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