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Revista Panamericana de Salud Pública logoLink to Revista Panamericana de Salud Pública
. 2017 Jun 19;41:e95. doi: 10.26633/RPSP.2017.95

Hospital-based tuberculosis control activities in five cities of Latin America

Actividades hospitalarias de control de la tuberculosis en cinco ciudades de América Latina

Atividades de controle da tuberculose em hospitais em cinco cidades da América Latina

Ralfh Moreno 1,, Rafael López 1, Alfonso Tenorio 1, Jorge Victoria 1, Anna Volz 1, Oscar Cruz 2, Ernesto Moreno 3, Carlos Quijada 4, Ana Hesse-de-Herrera 4, Sarita Aguirre 5, Laedi Santos 6, Noemi Lima 7, Neide Tanomaru 7, Antonieta Alarcon 8, Mirtha Del-Granado 1
PMCID: PMC6645313  PMID: 31384249

ABSTRACT

Objective.

To generate actionable insights for improving TB control in urban areas by describing the tuberculosis (TB) control activities of hospitals in five cities in Latin America.

Methods.

A descriptive study of hospital-based TB control activities was conducted in 2013–2015 using a cross-sectional survey designed by the Pan American Health Organization and administered in Guatemala City, Guatemala; Guarulhos, Brazil; Bogotá, Colombia; Lima, Peru; and Asunción, Paraguay. Data were analyzed using Chi-squared, Fisher exact tests, and the Mantel–Haenszel test for Risk Ratios, as necessary (P < 0.05).

Results.

While variation among cities existed, most hospitals (91.3%) conducted acid-fast bacilli smears for TB diagnosis and had a quality control process (94.0%), followed national TB guidelines (95%), and reported TB cases to the respective health authorities (96%). Additionally, TB treatment was offered free of charge almost universally (97.1%). However, only 74.2% of hospitals were supervised by the national or local TB programs; 52.8% followed up on the outcome of referrals; and 39.1% offered full ambulatory TB treatment, with 68.7% using Directly-Observed Therapy.

Conclusion.

The study underscored strengths and weaknesses in specific areas for TB control activities in hospitals and highlighted the importance and complexity of coordinating efforts among private and public hospitals and the various stakeholders. Local TB programs and health authorities should use these results to enhance the quality of TB-related actions in hospitals in similar settings.

Keywords: Tuberculosis, hospital services, cities, Brazil, Colombia, Guatemala, Paraguay, Peru, Latin America


Despite the remarkable health progress achieved by the Millennium Development Goals (1) at the global and regional levels, there remain substantial challenges for the prevention of death and disability due to communicable diseases (1). As recently as 2014, an estimated 9.6 million people developed active tuberculosis (TB) and 1.5 million died of the disease (2).

Particularly, in Latin America and the Caribbean, TB exhibits considerable variation. In 2013, for instance, TB incidence and mortality in Central America were 28 and 1.9 per 100 000, respectively; whereas in the Caribbean, these figures were as high as 70 and 8.3 per 100 000 (3), with some countries well above these averages (4). These areas of high burden represent a strategic priority in the TB elimination effort.

Beyond regional variations, TB is also influenced by urbanization. Cities tend to have a higher TB burden, especially in deprived areas where poverty, overcrowding, and poor sanitation are common (5). At the same time, a larger concentration of high-risk populations—the homeless, immigrants from high-incidence areas, drug users—further compounds the problem (6, 7).

Against this backdrop, the Pan American Health Organization (PAHO), with the support of the United States Agency for International Development (USAID) and local TB programs, developed an initiative to improve TB control in urban areas in the Region of the Americas. The “Framework for TB Control in Large Cities of Latin America and the Caribbean” (FTCLAC; 8) provides a comprehensive and multi-sectorial approach to TB control in urban areas, incorporating multiple actors and addressing key social determinants that perpetuate the disease, while taking into account the local health system structure (8).

Given the scarce information available on the practices of urban hospitals regarding patients with TB, a key component of the framework was to conduct a survey to address the gap. To this end, this study presents the findings from the FTCLAC hospital survey, with the aim of generating actionable insights that can be used to improve TB control activities at the hospital level across cities in Latin America.

MATERIALS AND METHODS

A descriptive study with analytical components was conducted on the basis of a multi-city, cross-sectional hospital survey carried out in 2013–2015. A hospital was defined as a health care institution with in-patient care (9).

Study instrument

The survey was developed by PAHO and consisted of three main sections: hospital identification, hospital characteristics, and activities related to TB control, for a total of 65 questions. In each institution, the tool was administered by up to two trained pollsters who followed a guidance document to ensure standardization. A pilot survey had been carried out at the San José del Callao Hospital, in Callao, Peru, in 2013. The survey was applied in hospitals of selected cities that were willing to participate and share results: Asunción (Paraguay), Bogotá (Colombia), Guarulhos (Brazil), Guatemala City (Guatemala), and Lima (Peru).

Study sample

The sampling was purposive, aiming to use a total population technique based on information provided by local health authorities. Importantly, the selection criteria for hospitals in each city varied according to the local context. In Guatemala City, the survey was administered in hospitals belonging to a “municipal health district” that included the neighboring area of Mixco; only hospitals of median or higher complexity (HMHC), defined as those having other types of medical services beyond general medicine, were surveyed in this city. In metropolitan Lima, only public, HMHC were covered. In Asunción, the target was the metropolitan area, with only public institutions participating. In Bogotá, public and private HMHC were surveyed. Lastly, in Guarulhos all hospitals were included.

The survey was conducted with the consent of national, local, and hospital authorities. Data was collected through interviews with administrative and clinical personnel at each participating hospital. Since the survey gathered aggregated information at the hospital level and no individual patient data whatsoever, ethical approval was not required.

Data analysis

Survey data was compiled and analyzed by PAHO. Descriptive statistics with some analytical components were conducted, and observations with missing data for the most relevant questions were not included in the analysis. Also, given that information from private hospitals was not available in some cities, the data was disaggregated by public/private hospitals to allow for more accurate comparisons across cities. When assessing statistical differences between categorical variables, a Chi-squared or Fisher exact test was used. The Mantel–Haenszel test for Risk Ratios (RR) was used to assess the magnitude of association and adjust for confounders, when necessary. P-values < 0.05 were considered statistically significant. The information was analyzed using Stata® 13.1 (StataCorp LP, College Station, Texas, United States).

RESULTS

Initially, 161 hospitals were invited to participate. All selected cities had a 100% response rate, except Guatemala City with 66%. Consequently, only 145 hospitals were surveyed. Moreover, given the volume of data missing from some hospitals surveyed in Guatemala City, two public and nine private hospitals were removed from the analysis. Likewise, two health care institutions in Bogotá and four in Asunción were not analyzed because they did not meet the inclusion criteria. Thus, a total of 128 institutions were included in the final analysis (Table 1). Hospitals were classified by size (based on the number of beds using terciles as cutoff points), public or private, and general or specialized. For Asunción and Lima, no data was collected from private hospitals.

TABLE 1. Characteristics of hospitals selected for a study on tuberculosis (TB) control activities in five cities in Latin America, 2013–2015.

Characteristics

Guatemala City

Bogotá

Guarulhos

Lima

Asunción

Total

n

%

n

%

n

%

n

%

n

%

n

%

Financing source

Public

10

47.6

20

29.4

5

38.5

17

100.0

16

100.0

68

53.1

Private

11

52.4

41

68.3

8

61.5

0

0.0

0

0.0

60

46.9

Hospital type

General

7

33.3

49

80.3

10

76.9

11

64.7

12

75.0

89

69.5

Specialized

14

66.7

12

19.7

3

23.1

6

35.3

4

25.0

39

30.5

Size

Small (< 70 beds)

13

61.9

15

24.6

3

23.1

2

11.8

8

50.0

41

32.0

Medium (70–195 beds)

4

19.1

21

34.4

7

53.9

4

23.5

2

12.5

38

29.7

Large (≥195 beds)

4

19.1

21

34.4

3

23.1

8

47.1

3

18.8

39

30.5

No data

0

0.0

4

6.6

0

0.0

3

17.7

3

18.7

10

7.8

Total

 

21

100.0

61

100.0

13

100.0

17

100.0

16

100.0

128

100.0

Source:Prepared by the authors based on the study data.

Across all cities, most public hospitals had a TB program, although in Guarulhos the number was low, just 20.0% (Table 2). With respect to care standards for people with active TB (PWAT), most hospitals used guidelines that followed national recommendations (96.0%). Notably, public hospitals in Guarulhos and private hospitals in Guatemala City were not subject to supervision by the respective TB program. With regard to TB contact tracing (TBCT), private institutions in Bogotá and public hospitals in Guarulhos did not conduct this activity (Table 2). Notably, there was a statistically significant correlation between hospital size and TBCT, with larger institutions being less likely to carry out tracing (P < 0.05). Lastly, most hospitals notified the national or local TB program once a patient was diagnosed with TB, with an overall average of 94.5%.

TABLE 2. Organization, guidelines, and supervision of tuberculosis (TB) activities in selected hospitals in five cities in Latin America, 2013–2015.

Variable

Guatemala City

Bogotá

Guarulhos

Lima

Asunción

Total

Public

Private

Public

Private

Public

Private

Public

Public

n

%

n

%

n

%

n

%

n

%

n

%

n

%

n

%

n

%

Number of hospitals

10

100.0

11

100.0

20

100.0

41

100.0

5

100.0

8

100.0

17

100.0

16

100.0

128

100.0

Presence of TB program

8

80.0

1a

9.1

20

100.0

40

97.6

1

20.0

2

25.0

16

94.1

14

87.5

102

79.7

Use of national TB diagnosis and treatment guidelines

10

100.0

4a, b

57.1

20

100.0

40

97.6

4

80.0

8

100.0

17

100.0

16

100.0

119

96.0

Hospital supervision by the national/local TB program

6

60.0

0a

0.0

19

95.0

37

90.2

0

0.0

3

37.5

16

94.1

14

87.5

95

74.2

TB contact tracing

4

40.0

3c

33.3

8

40.0

0a

0.0

0

0.0

2c

28.6

10

58.8

15

93.7

42

33.6

Notification of TB cases to national/local TB program

9

90.9

7

63.6

20

100.0

41

100.0

5

100.0

8

100.0

16

94.1

15

93.7

121

94.5

Source:Prepared by the authors based on the study data.

a

P< 0.05 when compared to the public sector of the same city.

b

Information available for 7 hospitals.

c

Information for private Guatemala City and Guarulhos available for 9 and 7 hospitals, respectively.

Overall, most hospitals conducted acid-fast bacilli smears (AFB), with an average of 91.3% (Table 3). In addition, among the hospitals that performed AFB, 94.0% conducted a quality control test. With respect to TB culture and drug susceptibility testing (DST), 44.4% and 6.8% of hospitals offered these, respectively; the Xpert®MTB/RIF assay (Xpert), which not only diagnoses TB, but also tests for resistance to Rifampicin, was included in the latter category. Hospitals in Guarulhos and public hospitals in Bogotá did not conduct DST. Of note, there was no available information on cultures and DST for private hospitals in Guatemala City.

TABLE 3. Availability of bacteriological tests and criteria for diagnosing tuberculosis (TB) in selected hospitals in five cities in Latin America, 2013–2015.

Variable

Guatemala City

Bogotá

Guarulhos

Lima

Asunción

Total

Public

Private

Public

Private

Public

Private

Public

Public

n

%

n

%

n

%

n

%

n

%

n

%

n

%

n

%

n

%

Number of hospitals

10

100.0

11

100.0

20

100.0

41

100.0

5

100.0

8

100.0

17

100.0

16

100.0

128

100.0

Availability of acid-fast bacilli test (AFB)

9

90.0

7a

70.0

19

95.0

39

95.1

4

80.0

6

75.0

17

100.0

15

39.7

116

91.3

    AFB quality control process

9

100.0

6

85.7

19

100.0

38

97.4

4

100.0

5

85.3

14

82.3

14

93.3

109

94.0

Availability of TB culture

3

30.0

12

60.0

20

48.8

3

60.0

2

25.0

9

52.9

3

18.7

52

44.4

Availability of drug susceptibility tests, including Xpert

3

30.0

0

0.0

3

7.3

0

0.0

0

0.0

1

5.9

1

6.2

8

6.8

Diagnosis based on:

    Symptoms

8

80.0

7

63.6

20

100.0

41

100.0

5

100.0

7

87.5

17

100.0

10

62.5

115

89.8

    Bacteriologyb

10

100.0

10

90.9

20

100.0

41

100.0

5

100.0

6

75.0

17

100.0

15

93.7

124

97.0

    Chest X-ray

7

70.0

8

72.7

20

100.0

40

97.5

4

80.0

7

87.5

17

100.0

9

56.2

112

87.5

    Other testsc

4

40.0

1

9.1

3

15.0

12

29.3

0

0.0

3

37.5

4

23.5

1

6.2

28

21.9

Source:Prepared by the authors based on the study data.

a

Information available for 10 hospitals.

b

Bacteriology includes acid-fast bacilli test, culture, and Xpert.

c

Includes biopsy, polymerase chain reaction (PCR), purified protein derivative (PPD), and computed tomography (CT scan).

In relation to TB diagnosis, most hospitals used bacteriological tests (Table 3), with an overall average of 97%. In general terms, hospitals in Bogotá and Lima always confirmed TB diagnosis using a combination of symptoms, bacteriology, and chest radiography.

Once a patient was diagnosed with TB, the case management varied significantly across cities. In Asunción, for example, 87.5% of hospitals started and continued treating patients on an ambulatory basis, whereas in Guarulhos neither public nor private hospitals did so (Table 4). When hospitals offered ambulatory TB treatment, on average 68.7% of them conducted Directly-Observed Therapy (DOT) (1st and 2nd phase). Notably, TB drugs were offered free of charge almost universally (97.1%), the exception being the private sector in Guatemala City (only 33.3%).

TABLE 4. Hospital management of patients with tuberculosis (TB) among selected hospitals in five cities in Latin America, 2013–2015.

Variable

Guatemala City

Bogotá

Guarulhos

Lima

Asunción

Total

Public

Private

Public

Private

Public

Private

Public

Public

n

%

n

%

n

%

n

%

n

%

n

%

n

%

n

%

n

%

Number of hospitals

10

100.0

11

100.0

20

100.0

41

100.0

5

100.0

8

100.0

17

100.0

16

100.0

128

100.0

Hospitals with full ambulatory TB treatmenta

4

40.0

2

18.2

11

55.0

10b

24.4

0

0.0

0

0.0

9

52.9

14

87.5

50

39.1

    Hospitals implementing both phases of directly-observed therapy

1

25.0

1

50.0

8c

80.0

5

50.0

NAd

NAd

NAd

NAd

7

77.8

11e

84.6

33

68.7

Free TB medication

10

100.0

1b,f

33.3

20

100.0

41

100.0

NAd

NAd

NAd

NAd

17

100.0

13g

92.9

102

97.1

Hospital refers patients to other facility for continuous treatmenta

7

70.0

11

100.0

19

95.0

41

100.0

5

100.0

4

50.0

15

88.2

6

37.5

108

84.4

    Verification of successful referral

4

57.1

5

45.4

11

57.9

24h

60.0

1

20.0

1

25.0

7

46.7

4

67.7

57

52.8

Hospitalization if necessarya

6

60.0

4

36.4

19

95.0

40

97.6

5

100.0

6

75.0

16

94.1

16

100.0

112

87.5

Hospital requests drug susceptibility test for patients suspected of having multidrug-resistant TB

7i

87.5

4i

100.0

18i

100.0

34i

100.0

15

88.2

13i

92.9

91

95.8

Hospital treats HIV/TB coinfected patients

8

80.0

2b

18.2

14

70.0

27

65.9

5

100.0

5

62.5

14

82.4

14

87.5

89

69.5

    Provision of Isoniazid preventive therapy in people living with HIV (PLHIV) without active TB

4

50.0

0

0.0

6

42.8

10

37.0

1j

33.3

0

0.0

11

78.6

4

28.6

36

41.4

    Provision of antiretroviral therapy in PLHIV with active TB

5

62.5

1

50.0

7

50.0

19

70.4

0

0.0

0

0.0

12

85.7

5

35.7

49

55.1

Source:Prepared by the authors based on the study data.

a

These activities can overlap.

b

P< 0.05 when compared to the public sector of the same city.

c

The public sector in Bogotáhad available information for 10 hospitals.

d

Not applicable

e

The public sector in Asunción had available information for 13 hospitals.

f

The private sector of Guatemala City had available information for 3 hospitals.

g

Asunción had available information for 14 hospitals.

h

Information available for 40 hospitals.

I

Information for public and private Guatemala, public and private Bogotáand Asunción available for 8, 4, 18, 34, and 14 hospitals, respectively

j

Available information for 3 hospitals.

Besides providing ambulatory TB treatment, most hospitals (84.4%) also referred PWAT to other institutions to continue therapy (Table 4). However, confirmation of successful referral only took place in 20.0% – 67.7% of hospitals, for a total average of 52.8%. Likewise, most hospitals (87.5%) offered TB inpatient care depending on the patient’s clinical condition. Regarding multidrug-resistant TB (MDR-TB), 95.8% of all hospitals requested DST when drug resistance was suspected.

It was found that, on average, 69.5% of hospitals treated people living with HIV (PLHIV) and co-infected with TB (Table 4). In these hospitals, TB screening in PLHIV was nearly universal and usually based on symptoms (99%); the percentage of patients initially diagnosed with active TB and then screened for HIV was also high, at 95%. In addition, the provision of Isoniazid preventive therapy (IPT) in PLHIV without active TB was found to be low across cities, with an average of 41.4%. Lima was a notable exception at 78.6%. For PLHIV with active TB, the provision of antiretroviral therapy (ART), overall, was 55.1%. Guarulhos had a figure of 0 since that city’s ambulatory ART was not provided in hospitals, but rather in HIV-specialized clinics.

In relation to TB infection control measures in health care settings, 90.5% of hospitals had an infection control committee, although Asunción had a low number, at 56.2% (Table 5). In addition, on average, only 34.1% of hospitals separated presumptive PWAT while in waiting rooms. Furthermore, only an average of 43.7% of hospitals conducted TB screening for clinical staff. Of note, public hospitals in Guatemala City, Guarulhos, and Lima had a high proportion of clinical staff with active TB. However, this difference was only statistically significant for Lima after comparing public hospitals among each other and either adjusting for hospital size (RR 2.54; 95% confidence interval [95%CI] = 1.57–4.12) or the presence of TB screening (RR 3.17; 95% CI = 1.72–5.82). In addition, despite the importance of proper ventilation for preventing TB transmission in health care settings, most hospitals did not provide enough, accurate information on this topic. Therefore, it was not possible to analyze nor include this variable in the study.

TABLE 5. Preventive measures and detection of tuberculosis (TB) transmission in hospital settings in five cities in Latin America, 2013–2015.

Variable

Guatemala City

Bogotá

Guarulhos

Lima

Asunción

Total

Public

Private

Public

Private

Public

Private

Public

Public

n

%

n

%

n

%

n

%

n

%

n

%

n

%

n

%

n

%

Number of hospitals

10

100.0

11

100.0

20

100.0

41

100.0

5

100.0

8

100.0

17

100.0

16

100.0

128

100.0

Hospital has an infection control committee

9

90.0

7a

70.0

20

100.0

40

97.6

5

100.0

8

100.0

17

100.0

9

56.2

115

90.5

    Includes TB control activities

8

88.9

4

57.1

16

80.0

34

85.0

4

80.0

7

87.5

12

70.6

6

66.6

91

79.3

Separation of presumptive people with active TB in waiting rooms

4

40.0

5b

55.5

1

5.0

16b

40.0

1

20.0

3

37.5

6

35.3

6b

42.9

42

34.1

    Patients use surgical masks

9c

100.0

6c

85.7

9d

45.0

31

75.6

5

100.0

8

100.0

17

100.0

13

81.2

98

79.7

Staff uses N95 masks

8e

88.9

4e

66.7

18

90.0

41

100.0

5

100.0

8

100.0

15

88.2

6e

42.9

105

87.5

Hospital staff screened for TB

2

20.0

7d

63.6

6

30.0

16

39.0

2

40.0

2

25.0

13

76.5

8

50.0

56

43.7

Hospital had cases of clinical staff with TB during the last year

4

40.0

1

9.1

5f

26.3

10

24.4

2

40.0

0f

0.0

13f , g

81.2

1

6.2

36

29.0

a

Available information for 10 hospitals.

b

Information for private Guatemala City, private Bogotá and Asunción available for 9, 40, and 14 hospitals, respectively.

c

Information for public and private Guatemala City available for 9 and 7 hospitals, respectively.

d

P < 0.05 when compared to public sector of the same city.

e

Information for public and private Guatemala City, and for Asunción available for 9, 6, and 14 hospitals, respectively

f

Information for public Bogotá, private Guarulhos and Lima available for 19, 6, and 16 hospitals, respectively.

g

P < 0.05 when compared to other public hospitals in other cities and after adjusting for possible confounders such as hospital size or the presence of a TB screening program.

Source: Prepared by the authors based on the study data.

DISCUSSION

Despite the heterogeneous sample, this study shed light on a subject for which there is little information in the Region. Given the large amount of information obtained in the results, only the most relevant outcomes were discussed.

Overall, most hospitals in the study used bacteriology coupled with symptoms as the main tools to diagnose TB—in line with current standards (10). In addition, AFBs usually underwent a quality control process. This is of particular importance given that high quality-assured bacteriology is a priority in TB control (11). Another trend across hospitals was the scarce verification of successful referral of PWAT. This is of particular concern since some lost-to-follow-up patients will not receive early treatment or any treatment at all, making clinical outcomes poorer and perpetuating the transmission of both TB and MDR-TB (12). In addition, hospitals rarely carried out TBCT. As explained in the results section, this is probably related to the institution’s size, which in turn is a proxy of a hospital’s complexity. Frequently, more complex health care institutions, such as those in Bogotá, Lima, and Guatemala City leave TBCT to public health authorities and/or to smaller, more primary health care focused hospitals like those in Asunción. Despite this, it is imperative that hospitals not offering TBCT do their utmost to ensure that patients are directed to facilities capable of comprehensive TB management and TBCT.

Regarding city trends, in Guatemala City a low proportion of both public and private hospitals conducted DOT. Moreover, several hospitals in the private sector were not willing to disclose information, and some charged for TB medication. Against this backdrop, closer surveillance of hospitals by the Guatemalan TB program and greater private hospital engagement are relevant factors to tackling TB transmission. With respect to Bogotá, the implementation of DOT in the private sector was considerably below the goal of 100% coverage, leaving room for improvement. It has to be clarified that many hospitals in Bogotá do not conduct TBCT, as this is a duty assigned to local public health authorities (13). Meanwhile, the high levels of ambulatory TB treatment and TBCT in Asunción are likely due to the public nature of the surveyed institutions, coupled with the fact that many of the hospitals were general and possibly primary health care oriented, as previously discussed.

In addition, it was found that health care workers in Lima had a higher risk of TB infection compared to other cities, a finding that is supported by other reports (14, 15). This may be partially due to the high local TB burden, among the highest in the Region (3).

In this study, many hospitals conducted AFB and diagnosed PWAT, but only a smaller proportion provided ambulatory TB treatment since most hospitals referred patients to other institutions. This appeared to be the case, particularly in Brazil, where on many occasions hospitals are the primary place in which TB is detected, but treatment is provided in primary health care facilities (16, 17). Despite this, public hospitals in Guarulhos and private ones in Guatemala City were not subject to supervision by the local TB program; were they, oversight could contribute to improvements in the quality of TB diagnosis and completion of referrals.

In addition, one of the key targets in TB control is the adequate management of TB/HIV (11). Surprisingly, IPT, which decreases the incidence of active TB in PLHIV (18, 19), was rarely implemented in most of the hospitals included in the study. Therefore, revision of institutional policies should be conducted to include TB prophylaxis as a regular practice in PLHIV without active TB. At the same time, it is worth noting that hospitals in our study reported higher ART coverage than that described by Regional reports (3). This could be due to either higher ART availability in urban areas compared to national averages, or to a higher provision of treatment in hospitals that care for TB/HIV coinfected patients.

Another important aspect of TB control is preventing its nosocomial transmission (20). It was found that relatively inexpensive TB infection control measures—use of surgical mask by patients, separation of presumptive PWAT in waiting rooms (20)—were not universally implemented. Additionally, most of the city hospitals conducted limited TB screening among their staff, despite that working in a health care facility is a risk factor for developing TB and MDR-TB (21). Consequently, stricter TB infection control measures, in coordination with hospital infection control committees, should be put in place.

Limitations

This study had limitations such as representativeness—the outcomes for Bogotá, Guatemala City, and Lima reflect only the actions taken by hospitals of higher complexity, whereas in Asunción and Guarulhos all complexity levels were surveyed. In addition, the results from Guatemala City, especially those from the private sector, are likely not representative given the number of excluded hospitals. This limitation was secondary to (i) their reluctance to participate in the survey and (ii) the large quantity of missing information for those that participated. Furthermore, the unwillingness of the private sector to disclose information was noteworthy.

Conclusion

This study found that hospitals in the surveyed cities are implementing, to various degrees, TB control activities. Many of these activities, however, need to be completed and/or enhanced, including supervision and standardization of TB diagnosis and treatment, TBCT, TB prophylaxis in PLHIV, and TB infection control measures at the institutional level. These results underscore the need to foster partnerships between the private and public sectors, as well as to coordinate among stakeholders and levels of care, especially with primary health care services. Local TB programs and health authorities may use these results to improve the quality of TB-related activities in the selected cities and in other similar settings in Latin America.

Acknowledgements.

This study was possible thanks to the collaboration of the national and local tuberculosis program of the countries in which the survey was conducted.

Funding.

The study was funded by the United States Agency for International Development (Washington, DC, United States; Grant 002140). This institution did not have any role in study design, data collection, data analysis, or decision to publish.

Disclaimer.

Authors hold sole responsibility for the views expressed in the manuscript, which may not necessarily reflect the opinion or policy of the RPSP/PAJPH and/or PAHO.

REFERENCES

  • 1.United Nations. The Millennium Development Goals Report . 2015. New York: UN; 2015. [Accessed on 19 November 2015]. Available from www.un.org/millenniumgoals/2015_MDG_Report/pdf/MDG%202015%20rev%20(July%201).pdf. [Google Scholar]; 1. United Nations. The Millennium Development Goals Report 2015. New York: UN; 2015. Available from: www.un.org/millenniumgoals/2015_MDG_Report/pdf/MDG%202015%20rev%20(July%201).pdf Accessed on 19 November 2015.
  • 2.World Health Organization . The end TB strategy. Geneva: WHO; 2015. [Accessed on 19 November 2015]. Available from www.who.int/tb/End_TB_brochure.pdf. [Google Scholar]; 2. World Health Organization. The end TB strategy. Geneva: WHO; 2015. Available from: www.who.int/tb/End_TB_brochure.pdf Accessed on 19 November 2015.
  • 3.Pan American Health Organization Tuberculosis in the Americas - Regional Report 2014. [Accessed on 20 November 2015];Washington DC: PAHO. 2014 Available from www.paho.org/hq/index.php?option=com_docman&task=doc_view&Itemid=270&gid=31283&lang=en. [Google Scholar]; 3. Pan American Health Organization. Tuberculosis in the Americas - Regional Report 2014. Washington DC: PAHO; 2014. Available from: www.paho.org/hq/index.php?option=com_docman&task=doc_view&Itemid=270&gid=31283&lang=en Accessed on 20 November 2015.
  • 4.World Health Organization . Tuberculosis country profiles. Geneva: WHO; 2015. [Accessed on 20 November 2015]. Available from www.who.int/tb/country/data/profiles/en/ [Google Scholar]; 4. World Health Organization. Tuberculosis country profiles. Geneva: WHO; 2015. Available from: www.who.int/tb/country/data/profiles/en/ Accessed on 20 November 2015.
  • 5.van Hest NA, Aldridge RW, de Vries G, Sandgren A, Hauer B, Hayward A, et al. Tuberculosis control in big cities and urban risk groups in the European Union: a consensus statement. Euro Surveill. 2014;19(9):20728. doi: 10.2807/1560-7917.es2014.19.9.20728. [DOI] [PubMed] [Google Scholar]; 5. van Hest NA, Aldridge RW, de Vries G, Sandgren A, Hauer B, Hayward A, . Tuberculosis control in big cities and urban risk groups in the European Union: a consensus statement. Euro Surveill. 2014;19(9):20728 [DOI] [PubMed]
  • 6.de Vries G, Aldridge RW, Cayla JA, Haas WH, Sandgren A, van Hest NA, et al. Epidemiology of tuberculosis in big cities of the European Union and European Economic Area countries. Euro Surveill. 2014;19(9):20726. doi: 10.2807/1560-7917.es2014.19.9.20726. [DOI] [PubMed] [Google Scholar]; 6. de Vries G, Aldridge RW, Cayla JA, Haas WH, Sandgren A, van Hest NA, . Epidemiology of tuberculosis in big cities of the European Union and European Economic Area countries. Euro Surveill. 2014;19(9):20726 [DOI] [PubMed]
  • 7.Ortblad KF, Salomon JA, Bärnighausen T, Atun R. Stopping tuberculosis: a biosocial model for sustainable development. Lancet. 2015;386(10010):2354–2362. doi: 10.1016/S0140-6736(15)00324-4. [DOI] [PMC free article] [PubMed] [Google Scholar]; 7. Ortblad KF, Salomon JA, Bärnighausen T, Atun R. Stopping tuberculosis: a biosocial model for sustainable development. Lancet. 2015;386(10010):2354–62. [DOI] [PMC free article] [PubMed]
  • 8.Pan American Health Organization Framework for tuberculosis control in large cities of Latin America and the Caribbean. [Accessed on 20 November 2015];Washington DC: PAHO. 2014 Available from www.paho.org/hq/index.php?option=com_docman&task=doc_view&Itemid=270&gid=29731&lang=en. [Google Scholar]; 8. Pan American Health Organization. Framework for tuberculosis control in large cities of Latin America and the Caribbean. Washington DC: PAHO; 2014. Available from: www.paho.org/hq/index.php?option=com_docman&task=doc_view&Itemid=270&gid=29731&lang=en Accessed on 20 November 2015.
  • 9.World Health Organization . Hospitals. Geneva: WHO; 2015. [Accessed on 21 November 2015]. Available from www.who.int/topics/hospitals/en/ [Google Scholar]; 9. World Health Organization. Hospitals. Geneva: WHO; 2015. Available from: www.who.int/topics/hospitals/en/ Accessed on 21 November 2015.
  • 10.Tuberculosis Coalition for Technical Assistance . International Standards for Tuberculosis Care (ISTC) The Hague: TBCTA; [Accessed on 23 November 2015 ]. 2006. Available from www.who.int/tb/publications/ISTC_3rdEd.pdf. [Google Scholar]; 10. Tuberculosis Coalition for Technical Assistance. International Standards for Tuberculosis Care (ISTC). The Hague: TBCTA; 2006. Available from: www.who.int/tb/publications/ISTC_3rdEd.pdf Accessed on 23 November 2015.
  • 11.World Health Organization & Stop TB Partnership . The Stop TB Strategy. Geneva: WHO; 2006. [Accessed on 23 November 2015 ]. Available from http://www.who.int/tb/publications/2006/who_htm_tb_2006_368.pdf. [Google Scholar]; 11. World Health Organization & Stop TB Partnership. The Stop TB Strategy. Geneva: WHO; 2006. Available from http://www.who.int/tb/publications/2006/who_htm_tb_2006_368.pdf Accessed on 23 November 2015.
  • 12.Millard J, Ugarte-Gil C, Moore DA. Multidrug resistant tuberculosis. BMJ. 2015;350 doi: 10.1136/bmj.h882. h882. [DOI] [PubMed] [Google Scholar]; 12. Millard J, Ugarte-Gil C, Moore DA. Multidrug resistant tuberculosis. BMJ. 2015;350:h882. [DOI] [PubMed]
  • 13.Ministerio de la Protección Social República de Colombia. Guía de atención integral de la tuberculosis pulmonar y extrapulmonar. [Accessed on 23 November 2015];Bogotá: Ministerio de la Protección Social; 2010. Available from www.quiminet.com/archivos_empresa/ed6336f2f12296476a01424588632b83.pdf. [Google Scholar]; 13. Ministerio de la Protección Social, República de Colombia. Guía de atención integral de la tuberculosis pulmonar y extrapulmonar. Bogotá: Ministerio de la Protección Social; 2010. Available from: www.quiminet.com/archivos_empresa/ed6336f2f12296476a01424588632b83.pdf Accessed on 23 November 2015.
  • 14.Bonifacio N, Saito M, Gilman RH, Leung F, Cordova Chavez N, Chacaltana Huarcaya J, et al. High risk for tuberculosis in hospital physicians. Peru. Emerg Infect Dis. 2002;8(7):747–748. doi: 10.3201/eid0807.010506. [DOI] [PMC free article] [PubMed] [Google Scholar]; 14. Bonifacio N, Saito M, Gilman RH, Leung F, Cordova Chavez N, Chacaltana Huarcaya J, . High risk for tuberculosis in hospital physicians, Peru. Emerg Infect Dis. 2002;8(7):747–8. [DOI] [PMC free article] [PubMed]
  • 15.Alonso-Echanove J, Granich RM, Laszlo A, Chu G, Borja N, Blas R, et al. Occupational transmission of Mycobacterium tuberculosis to health care workers in a university hospital in Lima, Peru. Clin Infect Dis. 2001;33(5):589–596. doi: 10.1086/321892. [DOI] [PubMed] [Google Scholar]; 15. Alonso-Echanove J, Granich RM, Laszlo A, Chu G, Borja N, Blas R, . Occupational transmission of Mycobacterium tuberculosis to health care workers in a university hospital in Lima, Peru. Clin Infect Dis. 2001;33(5):589–96. [DOI] [PubMed]
  • 16.Lemos EF, Alves AM. Oliveira GeC, Rodrigues MP, Martins ND, Croda J. Health-service performance of TB treatment for indigenous and non-indigenous populations in Brazil: a cross-sectional study. BMC Health Serv Res. 2014;14:237. doi: 10.1186/1472-6963-14-237. [DOI] [PMC free article] [PubMed] [Google Scholar]; 16. Lemos EF, Alves AM, Oliveira GeC, Rodrigues MP, Martins ND, Croda J. Health-service performance of TB treatment for indigenous and non-indigenous populations in Brazil: a cross-sectional study. BMC Health Serv Res 2014;14:237. [DOI] [PMC free article] [PubMed]
  • 17.Paula R, Lefevre F, Lefevre AM, Galesi VM, Schoeps D. Why do tuberculosis patients look for urgency and emergency unities for diagnosis: a study on social representation. Rev Bras Epidemiol. 2014;17(3):600–614. doi: 10.1590/1809-4503201400030003. [DOI] [PubMed] [Google Scholar]; 17. Paula R, Lefevre F, Lefevre AM, Galesi VM, Schoeps D. Why do tuberculosis patients look for urgency and emergency unities for diagnosis: a study on social representation. Rev Bras Epidemiol. 2014;17(3):600–14. [DOI] [PubMed]
  • 18.Churchyard GJ, Fielding K, Charalambous S, Day JH, Corbett EL, Hayes RJ, et al. Efficacy of secondary isoniazid preventive therapy among HIV-infected Southern Africans: time to change policy? AIDS. 2003;17(14):2063–2070. doi: 10.1097/00002030-200309260-00007. [DOI] [PubMed] [Google Scholar]; 18. Churchyard GJ, Fielding K, Charalambous S, Day JH, Corbett EL, Hayes RJ, . Efficacy of secondary isoniazid preventive therapy among HIV-infected Southern Africans: time to change policy? AIDS. 2003;17(14):2063–70. [DOI] [PubMed]
  • 19.Lawn SD, Wood R, De Cock KM, Kranzer K, Lewis JJ, Churchyard GJ. Antiretrovirals and isoniazid preventive therapy in the prevention of HIV-associated tuberculosis in settings with limited health-care resources. Lancet Infect Dis. 2010;10(7):489–498. doi: 10.1016/S1473-3099(10)70078-5. [DOI] [PubMed] [Google Scholar]; 19. Lawn SD, Wood R, De Cock KM, Kranzer K, Lewis JJ, Churchyard GJ. Antiretrovirals and isoniazid preventive therapy in the prevention of HIV-associated tuberculosis in settings with limited health-care resources. Lancet Infect Dis. 2010;10(7):489–98. [DOI] [PubMed]
  • 20.World Health Organization . WHO policy on TB infection control in health-care facilities, congregate settings and households. Geneva: WHO; 2009. [Accessed on 29 November 2015]. Available from http://apps.who.int/iris/bitstream/10665/44148/1/9789241598323_eng.pdf. [PubMed] [Google Scholar]; 20. World Health Organization. WHO policy on TB infection control in health-care facilities, congregate settings and households. Geneva: WHO; 2009. Available from: http://apps.who.int/iris/bitstream/10665/44148/1/9789241598323_eng.pdf Accessed on 29 November 2015. [PubMed]
  • 21.Baussano I, Nunn P, Williams B, Pivetta E, Bugiani M, Scano F. Tuberculosis among health care workers. Emerg Infect Dis. 2011;17(3):488–494. doi: 10.3201/eid1703.100947. [DOI] [PMC free article] [PubMed] [Google Scholar]; 21. Baussano I, Nunn P, Williams B, Pivetta E, Bugiani M, Scano F. Tuberculosis among health care workers. Emerg Infect Dis. 2011;17(3):488–94. [DOI] [PMC free article] [PubMed]

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