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Inicio Enfermedades Infecciosas y Microbiología Clínica (English Edition) Tuberculosis and immigration
Información de la revista
Vol. 36. Núm. 7.
Páginas 446-455 (agosto - septiembre 2018)
Visitas
3764
Vol. 36. Núm. 7.
Páginas 446-455 (agosto - septiembre 2018)
Continuing medical education: Mycobacterial infections
Acceso a texto completo
Tuberculosis and immigration
Tuberculosis e inmigración
Visitas
3764
Adrián Sánchez-Montalvá
Autor para correspondencia
, Fernando Salvador, Daniel Molina-Morant, Israel Molina
Departamento de Enfermedades Infecciosas, Hospital Universitario Vall d’Hebron, Universidad Autónoma de Barcelona, Programa de Salud Internacional del ICS (PROSICS), Barcelona, Spain
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Tablas (5)
Table 1. End TB strategy (2035).
Table 2. Immigrants in Spain from countries outside the European Union, rate of incidence, rate of incidence of MDR/RR by country (countries with communities of more than 50,000 people in Spain).
Table 3. Characteristics of the immigrant population with TB in Europe.
Table 4. Spanish studies comparing immigrant and native populations.
Table 5. Strategies for screening the immigrant population in developed countries with a low incidence of tuberculosisa
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Abstract

Tuberculosis continues to be a major public health problem in Spain. The incidence of tuberculosis in the native population has declined steadily in recent years. Migration flows have changed drastically since the beginning of the 21st century, with Spain becoming a recipient country for immigrants. Because most of the immigrants comes from countries with high incidence of tuberculosis, the contribution of the migrant population to new cases of tuberculosis is higher in relative terms than its weight in the total population. Tuberculosis programmes must address the cultural, economic and medical aspects of the disease, and particularly target groups at risk, including the migrant population. In this paper, we will review the epidemiology and dynamics of tuberculosis in the migrant population, their differentiating clinical characteristics and the programmatic actions to address the problem.

Keywords:
Tuberculosis
Immigration
Tuberculosis elimination
Tuberculosis control programmes
Resumen

La tuberculosis continúa siendo un problema de salud pública de primer orden en España. La incidencia de tuberculosis en la población autóctona ha disminuido progresivamente en los últimos años. Los flujos migratorios se han modificado drásticamente desde inicios del siglo xxi, cuando España ha pasado a ser un país receptor de inmigrantes. La mayor parte de los inmigrantes proceden de países con alta incidencia de tuberculosis, lo que ha supuesto que la contribución de esta población a los nuevos casos de tuberculosis sea relativamente superior respecto al peso que representan en el conjunto de la población. Los programas de lucha contra la tuberculosis tienen que abordar los aspectos culturales, económicos y médicos de la enfermedad, e incidir especialmente en los grupos de riesgo, entre los que destaca la población inmigrante. En este artículo revisaremos la epidemiología y la dinámica de la tuberculosis en la población inmigrante, sus características clínicas diferenciadoras y las acciones programáticas para abordar el problema.

Palabras clave:
Tuberculosis
Inmigración
Eliminación tuberculosis
Programas de control de la tuberculosis
Texto completo
Introduction

Tuberculosis (TB) remains a primary health concern the world over. Although the World Health Organization (WHO) declared it a global public health emergency in 1993, the necessary efforts have perhaps not been dedicated to controlling it on a global scale.1 According to the WHO, there were 10.4 million cases of TB worldwide in 2015, 3.1% of which were diagnosed in the European region, and 1.8 million people died as a result of TB.2 It has been estimated that a third of the global population is infected with Mycobacterium tuberculosis (M. tuberculosis), primarily in developing countries.3

The Global Plan to Stop Tuberculosis 2006–2015 launched by the WHO ended with mixed results by region. The new plan proposed by the WHO is meant to end the global epidemic of TB by 2035 (Fig. 1). Table 1 shows this plan's objective, indicators and pillars.4 Reaching this goal requires special attention to immigrant health and cooperation between countries.

Fig. 1.

Evolution of the incidence of tuberculosis under different scenarios.4Source: WHO end TB strategy: objectives and indicators.

(0.22MB).
Table 1.

End TB strategy (2035).

Goal 
End the global TB epidemic 
 
Indicators 
Reduction in number of TB deaths by 95% compared with 2015 
Reduction in TB incidence rate by 90% compared with 2015 
TB-affected families facing zero catastrophic costs due to TB 
 
Pillars 
Integrated, patient-centred care and prevention: broaden the scope and area of application of interventions for TB care and prevention, with an emphasis on high-impact, integrated and patient-centred approaches 
Bold policies and supportive systems: take advantage of all benefits of policies and systems for healthcare and development by involving a much broader set of collaborators from governments, communities and the private sector 
Intensified research and innovation: attempt to acquire new scientific knowledge and innovations that may dramatically change the landscape of TB prevention and care for patients with tuberculosis 
Immigration in Spain

Over time, migration movements in Spain have been influenced by the global economic crisis and numerous armed conflicts. It has been estimated that in 2015 there were close to 244 million international migrants and 66% of them migrated to developed countries.5 Although this decade started with historically high figures for the immigrant population (5,747,734 foreigners were recorded in a 2010 census, amounting to 12.2% of the Spanish population), the global economic crisis has brought about a decrease in the arrival of immigrants and has even created a negative migration balance in some regions of Spain (source: INE). Although most migration is voluntary, recent years have witnessed an increase in forced migration due to natural disasters, armed conflicts and political persecution.6 International protection was granted to 333,400 asylum seekers in the European Union in 2015, representing a 72% increase compared to 2014. In Spain, 15,755 people sought asylum in 2016. This figure was unprecedented. More than half of asylum seekers and refugees come from 4 countries: Syria (28%), Afghanistan (14%), Iraq (9%) or Nigeria (8%).7

With regard to TB, the significance of the origin of the people who come to Spain to seek new opportunities lies in the rate of incidence of TB in their countries of origin, as it will determine the number of recently acquired latent infections. For their part, the strains circulating in the countries of origin of the immigrant population may have different degrees of virulence and different patterns of resistance than TB strains in host countries2 (Table 2). Consequently, it is clear that the evolution of TB in Spain is going to be marked by migration movements and by measures that shall be taken as part of programmes to control TB, especially in populations with increased susceptibility to acquiring the infection and developing the disease, including the immigrant population.

Table 2.

Immigrants in Spain from countries outside the European Union, rate of incidence, rate of incidence of MDR/RR by country (countries with communities of more than 50,000 people in Spain).

Country  Total number of immigrants (INE: 1 January 2017)  Rate of incidence of TB per 100,000 (95% confidence interval)b  Rate of incidence of MDR/RR per 100,000 (95% confidence interval)b 
Morocco  700,429  107 (98–117)  1.7 (0.93–2.4) 
Romania  606,457  84 (72–97)  4.8 (3.7–5.6) 
Ecuador  408,690  52 (34–75)  4.6 (2.8–6.2) 
Colombia  362,152  31 (24–39)  1.2 (0.79–1.5) 
Venezuela  199,418  29 (22–36)  1.1 (0.61–1.6) 
Peru  190,867  119 (92–150)  10 (8.6–12) 
Argentina  255,671  25 (22–29)  1.2 (0.85–1.6) 
Dominican Rep.  164,259  60 (44–78)  2.7 (1.5–3.7) 
China  161,969  67 (57–77)  5.1 (4–6.1) 
Bolivia  148,761  117 (76–167)  4.7 (2.3–6.9) 
Cuba  139,283  7 (6–8.1)  0.22 (0.1–0.35) 
Brazil  108,027  41 (35–47)  1.1 (0.91–1.3) 
Portugala  107,065  23 (20–27)  0.3 (0.1–0.4) 
Ukraine  92,696  91 (59–130)  49 (38–60) 
Russia  86,086  80 (69–92)  42 (34–49) 
Uruguay  74,383  30 (26–35)  0.2 (0.0–0.4) 
Paraguay  63,406  41 (35–47)  1.3 (0.66–2) 
Honduras  56,738  43 (36–51)  1.4 (0.72–2.1) 
Algeria  56,524  75 (58–94)  1.2 (0.35–2) 
Chile  55,970  16 (14–19)  0.3 (0.2–0.4) 
Pakistan  53,980  270 (175–386)  14 (8.5–19) 
Mexico  52,524  21 (17–25)  0.7 (0.5–0.8) 
Senegal  51,076  139 (90–198)  2.7 (1.7–3.8) 

INE: Spanish National Statistics Institute; MDR/RR: multi-drug-resistant or rifampin-resistant tuberculosis; TB: tuberculosis.

a

Portugal has been included despite belonging to the European Union as it has a higher rate than Spain.

b

www.who.int/tb/data, accessed 29 September, 2017.

Contribution of immigration to the total burden of tuberculosis

TB in developed countries has exhibited an abrupt decline in the last quarter century, with incidences below 40 cases per 100,000 inhabitants.8 At present, TB in countries with a low incidence (<100 cases per million inhabitants) is primarily diagnosed in immigrants from countries with a high incidence (>100 cases per million inhabitants) and in patients with immunosuppression, such as transplant recipients, oncology/haematology patients, patients with immunosuppression caused by drugs and patients with immunosenescence.8 Some European countries with a low incidence of TB have experienced a less-abrupt-than-expected drop in their rates of TB. This has been found to be closely linked to the increase in the number of immigrants from countries with a high incidence of TB (Fig. 2).9 According to data from the European Centre for Disease Prevention and Control, more than 25% of cases of TB in Europe are diagnosed in individuals born in foreign countries. France, Germany, Spain and the United Kingdom account for approximately 75% of all these cases.8 In recent years, the number of cases of TB in the European Union/European Economic Area decreased by 5% annually; however, the number of cases of TB in immigrants increased by 6.8%.10 In Spain, during the period 2007–2013, 49,222 cases of TB were reported; of these, 30.6% (15,058) were diagnosed in patients not born in Spain. In general, the incidence of cases of TB in the immigrant population is linked to the incidences of TB in the country of origin.11

Fig. 2.

Tuberculosis reporting rates in immigrants and native individuals and proportion of cases of TB diagnosed in immigrants out of the total number of cases. Source: Framework towards tuberculosis elimination in low-incidence countries. Geneva: World Health Organization; 2014.

(0.39MB).

One of the most strongly debated subjects is the possibility of native cases increasing as a result of interaction with the immigrant population. However, many studies have shown that, although secondary cases may occur following contact with immigrants with TB, this does not represent a major public health problem, and in general transmission of TB from immigrants to the native population is limited.12,13 A molecular epidemiology study conducted in Italy showed that of 1080 cases (614 native and 466 immigrant) of TB with a positive culture, 12.9% of native cases were due to transmission by the immigrant population.14 Moreover, transmission from native patients to the immigrant population has also been documented.15 In a dynamic, modern and integrationist society, the flow of TB infections is bidirectional and depends heavily on the interaction of immigrants in the host community.13

Worldwide, there are different lineages of M. tuberculosis (lineage 1–lineage 7) (Fig. 3). Lineage 4 is the most widespread, probably due to intrinsic factors and patterns of human migration throughout history.16 It has been postulated that exploration and the Spanish and Portuguese conquests underlie the global spread of lineage 4, especially its sub-lineage L4.3/LAM. Each lineage may have several sub-lineages that predominate in different geographical areas and determine its pathogenic characteristics.16 It has been indicated that at least one genotype of M. tuberculosis (Beijing strain, lineage 2) may be more aggressive and more prone to acquiring resistance.17–20 Migration movements are blurring the boundaries of the geographic distribution of lineages and are painting a motley picture which makes it difficult to predict the potential impact on global patterns of transmissibility and pathogenicity. Moreover, resistance to first-line anti-tuberculosis drugs tends to be greater in patients from countries with a high incidence of TB. Patients with multi-drug-resistant (MDR) TB, i.e. TB resistant to isoniazid and rifampin, are concentrated in China, India, former Soviet Union countries and southern Africa. Until recently, it was believed that MDR TB paid the price of a decreased fitness by acquiring resistance mutations and that its transmissibility was decreased. However, in many countries, MDR TB is primarily acquired through contact with a bacilliferous patient and its rate of transmissibility is similar to that of multi-drug-sensitive TB.21,22

Fig. 3.

Lineages of TB. Taken from Brites and Gagneux.58

(0.35MB).

All this underscores the fact that eradicating TB in countries with a low incidence means working to control TB in migrant source countries, as well as implementing specific programmes to control TB in immigrants in host countries. If a massive influx of immigrants is not accompanied by a comprehensive healthcare programme that includes a standardised screening strategy for imported diseases as well as health promotion and access measures, rates of TB and resistance to first-line drugs may rise in the coming years.23 On an economic level, investment by host countries in the national programmes of immigrant source countries has been shown to economically benefit host countries.24

Risk of developing tuberculosis in the host country (reactivation vs acute infection)

The risk of an immigrant having TB is closely related to host factors, pathogen factors and the interaction between them. Initially, the risk of acquiring a TB infection will be determined by the rate of TB in the community. This in turn will depend on individual factors, living and working conditions, contamination, infrastructure, and healthcare programmes implemented to control TB. Moreover, host factors (concomitant diseases, malnutrition, smoking, etc.) and pathogen factors (virulence, initial infection, etc.) will ultimately modulate the risk of infection or reactivation of a recent or past infection.25

TB in immigrants is primarily due to reactivation of a latent tuberculosis infection (LTI) acquired prior to the migration process. However, there is also the possibility of the patient arriving with active TB or the infection occurring in the host country due to deficient living and working conditions.12,26 Some studies in Spain have found that 22%–28% of cases of TB diagnosed in the immigrant population belonged to clusters, thus pointing to transmission in the host country.27,28 Indeed, some studies have indicated that recent infections in the host country significantly contribute to the disease burden in the immigrant population.29

The diagnosis of TB in immigrants generally occurs within 3 years of their arrival in the host country.30,31 The risk of having TB in immigrants seems to be equivalent to that of the population of the host country 10 years after arrival32; however, the risk may persist for a longer period of time.33 Immigrants who travel often to their countries of origin have a higher risk of having TB due to an acute infection during their travels, especially when these exceed 3 months.34

Although LTI reactivation constitutes the primary mechanism by which TB is acquired in the immigrant population, the dynamics of TB in our society have many subtleties to bear in mind, including the possibility of acute infections in the host country and the risk of infection during sojourns in countries of origin.

Healthcare access and barriers for the immigrant population

Managing social determinants and risk factors associated with TB means enacting policies to decrease poverty, increase food safety, improve living conditions, stop smoking and alcohol use, and prevent development of diabetes mellitus. All this falls under universal healthcare coverage, understood as the provision of comprehensive and high-quality healthcare services for all with no need for a great deal of economic expenditure.4 A framework for action that fails to encompass this big-picture view of the problem will not succeed in eradicating TB.

In general, immigrants are healthy when they arrive from their country of origin (“effect of the healthy immigrant”)35 and their health needs overlap with those of the native population. However, several studies have found that, as time goes by, inequality in social welfare and healthcare sets in due to immigrants’ low socio-economic status, insufficient adaptation to social welfare and healthcare services, cultural and language barriers, and, in some cases, legal restrictions inherent to healthcare and social welfare systems.36

In general, difficulty accessing healthcare systems in host countries causes delayed diagnosis of TB in an individual37,38 and secondarily causes an increase in transmission among that individual's contacts. A study published in Spain in 2014 analysed a total of 20 studies that evaluated immigrant access to healthcare services in that country.39 In general, due to the universal nature of Spanish healthcare until 2012, no major differences were observed in the use of primary care between the immigrant population and the native population. Differences revealed themselves by geographic area (those from Eastern Europe and sub-Saharan Africa used fewer healthcare resources) and with respect to specialised medical care (the immigrant population had less access).40 Greater use of emergency services on the part of this population was also seen.39

The immigrant population perceives TB as a serious but curable disease, yet harbours many fears related to the possibility of infecting other people, being stigmatised or suffering possible consequences in their social relationships and occupational status. Once treatment has started, family support and the doctor–patient relationship are key to ensuring good adherence. The concept of LTI is difficult for the immigrant population to understand, although in general immigrants are quite amenable to screening. Patient-centred TB programmes aimed at early diagnosis of active TB and LTI in people at risk of reactivation would go a long way towards decreasing TB rates in the immigrant population. To achieve this aim, these programmes must be developed with consideration for the barriers that immigrants encounter and the professionals who implement these programmes must be aware of this.41 Information campaigns that inform immigrants about TB and the healthcare system have been shown to reduce diagnostic delays and stigma.42

Characteristics of tuberculosis in the immigrant population

Throughout the European Union, immigrant patients with TB tend to be HIV-negative men between the ages of 25 and 44 with pulmonary impairment who have received no prior treatment. The percentage of cases with a microbiologically-confirmed diagnosis, as well as an available antibiogram, is higher than in the native population. Resolution rates have been found to be above those for TB in native patients.10 Rates of resistance to anti-tuberculosis drugs are usually higher in the immigrant population; however, as with other characteristics, they will be determined by the countries of origin and characteristics of the immigrant population. Therefore, being familiar with the characteristics of the immigrant population is essential for dealing with cases of TB in this population, since these emulate the characteristics present in their countries of origin.26 More information is available in Table 3.

Table 3.

Characteristics of the immigrant population with TB in Europe.

  EU/EEC  Non-EU total  Eastern Mediterranean  Southwest Asia  Africa  Europe (non-EU/EEC)  Western Pacific  Americas 
Period    2007–2013
Total no.  399,613 (81.3%)  91,925 (187%)  26,945 (29.3%)a  21,097 (23%)a  19,629 (21.4)a  12,280 (13.4)a  6697 (7.3)a  5277 (5.7%)a 
Male  66.1%  57.8%  60.7%  57%  59.4%  60.1%  46.5%  49.1% 
<45 years  45%  71.8%  72.8%  74.6%  79.1%  51.7%  73.6%  73.7% 
Pulmonary  83.6%  57.8%  51%  43.7%  60.9%  82.8%  64%  70.9% 
Microbiological confirmation  53.7%  52.1%  51.7%  58.2%  46.9%  63.1%  53.4%  22.7% 
HIV  4.8%  9.6%  2%  4.8%  24.3%  9.5%  3.3%  9.4% 
Treatment success  74.6%  77.4%  80.4%  77.8%  77.8%  70.4%  75.4%  81.1% 
MDR  5.9%  2.9%  1.5%  1.9%  1.6%  9.6%  2.4%  1.4% 
a

Percentage of all immigrants.

Adapted from Kodmon C, Zucs P, van der Werf MJ. Migration-related tuberculosis: Epidemiology and characteristics of tuberculosis cases originating outside the European Union and European Economic Area, 2007 to 2013. Euro Surveill. 2016;21(12).

The form of presentation is not consistent throughout all studies; however, it seems that immigrant patients are diagnosed with extra-pulmonary forms more often than native patients. Of course, the pulmonary form is predominant in both populations.38,43 These variations may probably be explained by host factors and mycobacteria-related factors (mycobacteria sub-lineage and virulence factors). On a radiological level, immigrant patients have a higher rate of cavitated lesions and consequently a higher rate of bacilliferous TB.9,38,43Table 4 shows a selection of the most important Spanish studies comparing the characteristics of native and immigrant populations.

Table 4.

Spanish studies comparing immigrant and native populations.

  Morales-García et al.38
 
Arce-Arnáez et al.59  Ramos et al.60
 
Diz et al.61
 
Sánchez et al.62  Navarro et al.63  Borrell and Gagneux27
 
Study type  Retrospective  Retrospective  Retrospective  Retrospective  Retrospective  Retrospective  Retrospective 
Period  2003–2010  1994–2003  1999–2002  1990–2002  2000–2003  1997–2002  2003–2004 
Total no.  319  2211  105  1397  125  289  892 
No. of immigrants  72  269  22  98  60  14  309 
Mean age  N/A  N/A  28.7b  30  31  N/A  N/A 
Male  59.7%  61%b  72.7%  54%  75%  N/A  64% 
Country of origin  Romania 35%
Morocco 21%
Bolivia 10% 
Latin America 56.1%
Africa 29.7%
Europe 11.2%
Asia 3% 
Morocco 22.7%
Colombia 18.2%
Ecuador 18.2%
Romania 13.6% 
Peru 26.5%
Ecuador 15.3%
Eq. Guinea 8.1% 
Pakistan 29%
Morocco 12%
India 7%
Peru 5% 
Africa 28.6%
Latin America 21.4%
Asia 21.4% 
South America 40.8%
Asia 30.7%
North Africa 12.3% 
<35 years  65.3%a  60.2%a  N/A  N/A  N/A  N/A  <50, 92.5%a 
Pulmonary  88.9%  71%  81.8%a  79%  44%b  71.4%  66%b 
Cavitation  32.8%a  N/A  85%a  49%  N/A  N/A  N/A 
Bacilliferous  45.8%a  N/A  63.2%  70%  N/A  N/A  53.4% 
Microbiological confirmation  88.9%  N/A  N/A  83%  N/A  100%  N/A 
HIV  0%  13%b  9.1%  6%b  24%  21.4%  12.3% 
Diabetes  1.4%  N/A  N/A  N/A  N/A  N/A  0.6%b 
Non-HIV IS  0%  N/A  N/A  N/A  N/A  N/A  N/A 
Total diagnostic delay
(days) 
31.5 (mean)  33 (median)  N/A  N/A  N/A  N/A  N/A 
Visit delay (days)  12.5 (mean)a  N/A  N/A  N/A  N/A  N/A  N/A 
Treatment success  84.6%  42.8%a  54.5%  31%  50%  N/A  N/A 
H-monoresistance  1.51%  N/A  9.2%  9–13%a  N/A  N/A  3.8%d 
MDR  0%  N/A  N/A  N/A  1.6%  N/A  2.5%d 
  Peñaranda et al.64
 
Tirado Balaguer et al.65  Santiyán et al.66  Millares Lozano et al.67  García-García et al.43
 
Martínez-Lirola et al.29  Sanz Barbero and Blasco Hernández68 
Study type  Retrospective  Retrospective  Retrospective  Retrospective  Prospective  Retrospective  Cross-sectional 
Period  1999–2003  1995–2003  2003–2012  2005  2006–2007  2003–2006  2013 
Total no.  408  644  1667  104  1490  394  296 
No. of immigrants  89  84  620  22  442  211  296 
Mean age  31  N/A  32.29b  30b  N/A  30b  30 
Male  65%  N/A  63.2%  61.9%  60.2%  N/A  66.2% 
Country of origin  Morocco 20%
Ecuador 16%
Nigeria 5%
Senegal Romania 5%
India 5% 
Romania 36.9%
Morocco 23.8%
Colombia 7.1% 
Bolivia 18.39%
Romania 14.52%
Ecuador 12.42%
Pakistan 6.93% 
Latin America 27.8%
North Africa 27.8%
Sub-Saharan Africa 27.8% 
Romania 13.9%
Bolivia 13.5%
Morocco 11.5%
Pakistan 9.5% 
Morocco 39.8%
Romania 15.6%
Senegal 7.6%
Mali 6.6% 
Ecuador 27.4%
Morocco 19.3%
Romania 9.8% 
<35 years  N/A  N/A  N/A  N/A  <50, 93.5%a  N/A  N/A 
Pulmonary  67%  N/A  N/A  71.4%b  79.2%b  N/A  N/A 
Cavitation  N/A  N/A  N/A  36.8%  N/A  N/A  N/A 
Bacilliferous  N/A  N/A  39.5%a  N/A  60%  N/A  N/A 
Microbiological confirmation  100%  100%  N/A  N/A  77.2%  100% (inclusion criterion)  N/A 
HIV  23.6%  N/A  12.35%b  33.3%  4.3%  N/A  8.3% 
Diabetes  N/A  N/A  2.3%b  N/A  N/A  N/A  3.3% 
Non-HIV IS  N/A  N/A  N/A  N/A  N/A  N/A  N/A 
Total diagnostic delay (days)  N/A  N/A  N/A  45.5  42 (21–91)  N/A  N/A 
Visit delay (days)  N/A  N/A  N/A  N/A  N/A  N/A  N/A 
Treatment success  85.5%  N/A  N/A  N/A  83.5%b  N/A  N/A 
H-monoresistance  N/A  10.1%  N/A  8.3%  8.6%a  9.3%  N/A 
MDR  0%  0%    0%  2.7%a  1%  N/A 
  Ospina et al.30  Soler Rangel et al.69  Basterrechea et al.70  Navascués Ortega et al.71  Ordobás Gavín et al.72  Ruiz López et al.73 
Study type  Retrospective  Retrospective  Retrospective  Retrospective  Retrospective  Retrospective 
Period  1991–2013  1997–2006  2003–2007  2000–2007  1996–2004  1999–2004 
Total no.  3284  832  903  457  10,268  158 
No. of immigrants  3284  311  94  120  2067  66 
Mean age  N/A  32.37b  31b  N/A  N/A  29.9b 
Male  65.7%  59.8%b  63%  N/A  N/A  N/A 
Country of origin  Latin America 37.3%
Indian sub-continent 26.6%
 
Ecuador 25%
Morocco 17%
Romania 12%
Peru 11% 
Morocco 26.6%
Ecuador 10.6%
Pakistan 9.6%
 
Latin America 36.6%
North Africa 28.3%
Western Europe 14.2%
Sub-Saharan Africa 8.3% 
N/A  N/A 
<35 years  64%c  N/A  77.6%  N/A  N/A  N/A 
Pulmonary  58.1%  100%  68.1%  N/A  73.79%  N/A 
Cavitation  32.3%  78.8%b  N/A  N/A  N/A  N/A 
Bacilliferous  48.2%    34%  N/A  N/A  N/A 
Microbiological confirmation  N/A  91.7%  72.3%  100%  N/A  N/A 
HIV  10%  6.4%b  5.3%  N/A  N/A  N/A 
Diabetes  2.8%  3.5%b  N/A  N/A  N/A  N/A 
Non-HIV IS  N/A  0.3%  4.3%e  N/A  N/A  N/A 
Total diagnostic delay (days)  N/A  N/A  68  N/A  N/A  N/A 
Visit delay (days)  N/A  N/A  N/A  N/A  N/A  N/A 
Treatment success  84%  74%  79.8%b  N/A  N/A  N/A 
H-monoresistance  9.2%  8.3%  N/A  11.6%  N/A  10.2% 
MDR  2.1%  4%  0%  2.5%  N/A  2.1% 
a

Result statistically significantly higher than that of native individuals.

b

Result statistically significantly lower than that of native individuals.

c

Patients under 45 years of age.

d

New cases (Category 1).

e

Includes chronic diseases.

Causes of delayed diagnosis vary by patient origin, but are primarily lumped under outside reasons related to the healthcare system, or individual reasons such as fear of being reported to the authorities, losing their job, being kicked out of their homes or enduring the stigma associated with the disease. In general, native patients have a higher number of risk factors for developing active disease, such as HIV infection, parenteral drug use, smoking, alcoholism, diabetes, immunosuppression, chronic kidney failure and immunosenescence. These also underlie the greater mortality in the native population.9,38,43 In addition, contacts of immigrants with TB have higher rates of latent infections and active disease than contacts of native individuals with TB.38

In general, immigrants with TB wait longer after developing symptoms to seek medical assistance. However, once they enter the healthcare system, they are diagnosed earlier than native patients, probably due to a stronger diagnostic suspicion on the part of the healthcare staff. This divide is not as sharp in cases of patients with bacilliferous pulmonary TB.38 In general, immigrants are diagnosed in the emergency department at a higher rate than the native population.43

The same diagnostic techniques are used in the two groups. The introduction of molecular techniques has helped to reduce the length of diagnostic delays, particularly in patients without bacilliferous TB and with HIV infection. This aids in starting treatment early and decreasing transmission.44 With regard to drug resistance, studies conducted in Spain have yielded mixed results. Monoresistance to isoniazid ranges from 1.5% to 10.2% (Table 4). Fortunately, diagnoses of MDR TB remain very few and far between.43 It is likely that rates of resistance to anti-tuberculosis drugs in the immigrant population correspond to rates of resistance reported by countries of origin. Therefore, resistance may be inferred through familiarity with the local immigrant population.

The choice of anti-tuberculosis treatment is made with consideration for individual patient characteristics such as pregnancy status, concomitant medication, prior anti-tuberculosis treatments, comorbidities and patterns of resistance. Until an antibiogram is available, at least 4 drugs believed to be active against the patient's strain of M. tuberculosis will be used.45 There seem to be no differences in terms of treatment toxicity. Treatment success, which includes completed treatment and microbiological resolution, is similar in the two groups. However, immigrant patients stop treatment more often than the native population, and native patients have higher mortality rates in the course of treatment due to their greater comorbidity rates and older age.38,43,46 Stopping treatment in the immigrant population in Spain has been linked to being male, not living with any family members and moving to other communities. To these must be added other known variables such as prior anti-tuberculosis treatment, poor understanding of the disease and parenteral drug use.47,48 To maintain a good success rate, it is necessary to have a programme centred on patient needs that includes interventions in all sociocultural matters. It is also necessary to have economic resources to fund strategies such as directly observed treatment and community health agents.43,49

At present, a wide range of drugs and combinations is available to treat LTI.50 The choice of treatment for LTI in immigrants and native patients must be made with a view to the pattern of resistance of the index case if known; otherwise, any regimen having been shown to reduce reactivation of the disease shall be used.

Proposals for decreasing tuberculosis in the immigrant population

Efforts to control TB, especially in countries with a low incidence such as Spain, should place a special emphasis on risk groups such as immigrants, since these groups may have limited access to means of TB prevention, diagnosis and treatment.51 The WHO and the International Organization for Migration have proposed a number of efforts to decrease the incidence of TB in the immigrant population. These efforts urge the development of national TB plans that are inclusive with intersectoral and cross-border immigration, policies and systems, and operational research.52

Clearly, to decrease the incidence of TB in the immigrant population, the host country should ensure that everybody who has TB or requires preventive measures be able to access diagnostic tests, treatment and preventive measures. This means developing political and administrative measures (universal access to healthcare, ease of obtaining a healthcare card, etc.), raising awareness among healthcare staff and educating this population in using the healthcare system.53

Screening of the immigrant population is a cornerstone of these programmes for TB control. In the area of prevention, screening of this population is essential to find both active cases and people with LTI. Although screening algorithms are highly variable, more and more data are emerging that indicate that the most cost-effective strategy would be to perform an IGRA test in people under 35 years of age from a country with a high incidence of TB.54 Interventions may be classified as pre-travel or on-arrival depending on when screening is performed. The objective of screening performed in the country of origin (pre-travel) is to diagnose active disease to prevent transmission in the host country. When the programme is carried out in the host country, it is often broadened to include testing for LTI55 (Table 5). From a practical perspective, with a view to proper implementation, it is essential to involve and train primary care practitioners, as primary care is where this population is most likely to come into contact with the healthcare system.

Table 5.

Strategies for screening the immigrant population in developed countries with a low incidence of tuberculosisa

Country  Incidence of TB per 100,000 (2006)  Rate of TB in immigrants (%)  Programme objective  Migration pre-travel screening programme  Migration post-travel screening programme  LTI screening 
United States  4.6  57  Active TB  Yes  Yes  No 
United Kingdom  15  73  Active TB  Yes  Yes  No 
Germany  6.6  43.3  Active TB  No  Yes  No 
France  8.5  45  Active TB  No  Yes  No 
Spain  18.3  25  N/A  No  No  No 
Italy  7.5  46.2  N/A  No  No  No 
Canada  64  Active TB  Yes  Yes  No 
Australia  5.8  81.6  Active TB  Yes  Yes  No 
Japan  22  N/A  No  No  No 
a

There is significant variation within the programme itself depending on type of migrant, length of stay and profession as well as special situations (e.g. adoptions). The table above provides an overview of the situation.

ITL: latent tuberculosis infection; N/A: not applicable; TB: tuberculosis.

Adapted from Alvarez et al.55

The likelihood of an immigrant patient having MDR TB will vary depending on his or her geographic area of origin. Although the number of cases of MDR TB in Spain is low, this disease represents a growing problem that is generating concern.43 To address this problem, reference hospitals must have laboratories equipped with suitable diagnostic tools, including molecular biology techniques for early detection of resistance to anti-tuberculosis drugs. In addition, specialist practitioners with experience in treating and following up these patients are needed, since these patients need complex treatments and experience high rates of adverse effects.44

TB programmes should be patient-centred. This takes on greater importance in immigrant patients, since their social, cultural and religious realities may be very different from those of the native population. These sociocultural differences may tremendously alter the patient's perception of the disease and the healthcare system, with repercussions for disease prognosis and transmission.47 Hence the increasing emphasis on the importance of creating specialised units for managing patients with TB, which feature not only physicians, microbiologists and nurses but also professionals such as case managers (with experience in treatment adherence and contact study) and community health agents.

Finally, this type of population must be taken into account in TB research and figure among its priorities. Operational research is necessary to evaluate different strategies that ensure equitable healthcare access for all immigrants and to develop innovative tools for prioritising and identifying populations at risk.56,57

Limitations

This article was not prepared according to the standards of a systematic review. As a result, it is subject to article selection bias. Although many surveillance systems in Europe and Spain are solid, it is impossible for a system to record all migrations and cases of TB. These limitations notwithstanding, the information provided herein constitutes a useful review on the topic of immigration and TB.

Conclusion

TB in countries with a low incidence of TB is approaching eradication in the next few decades. When this objective will be achieved depends on the implementation of programmes that include the immigrant population among their priority objectives, as this population accounts for a significant percentage of active cases of TB diagnosed in countries with a low incidence of TB. Creating a patient-centred system that addresses social, cultural and economic considerations will help to accelerate the eradication of TB.

Conflicts of interest

There are no conflicts of interest.

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Please cite this article as: Sánchez-Montalvá A, Salvador F, Molina-Morant D, Molina I. Tuberculosis e inmigración. Enferm Infecc Microbiol Clin. 2018;36:446–455.

Copyright © 2017. Elsevier España, S.L.U. and Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica
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