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A tuberculin skin test survey among Ghanaian school children

  • Kennedy Kwasi Addo1Email author,
  • Susan van den Hof3, 4,
  • Gloria Ivy Mensah1,
  • Adukwei Hesse5,
  • Christian Bonsu1,
  • Kwadwo Ansah Koram2,
  • Felix Kwami Afutu6 and
  • Frank Adae Bonsu6
BMC Public Health201010:35

DOI: 10.1186/1471-2458-10-35

Received: 22 September 2009

Accepted: 26 January 2010

Published: 26 January 2010

Abstract

Background

Ghana has not conducted a national tuberculin survey or tuberculosis prevalence survey since the establishment of the National Tuberculosis Control Programme. The primary objective of this study was therefore to determine the prevalence of tuberculin skin sensitivity in Ghanaian school children aged 6-10 years in 8 out of 10 regions of Ghana between 2004 and 2006.

Methods

Tuberculin survey was conducted in 179 primary schools from 21 districts in 8 regions. Schools were purposively selected so as to reflect the proportion of affluent private and free tuition public schools as well as the proportion of small and large schools.

Results

Of the 24,778 children registered for the survey, 23,600 (95.2%) were tested of which 21,861 (92.6%) were available for reading. The age distribution showed an increase in numbers of children towards older age: 11% of the children were 6 years and 25%, 10 years. Females were 52.5% and males 47.5%. The proportion of girls was higher in all age groups (range 51.4% to 54.0%, p < 0.001). BCG scar was visible in 89.3% of the children. The percentage of children with a BCG scar differed by district and by age. The percentage of children with a BCG scar decreased with increasing age in all districts, reflecting increasing BCG vaccination coverage in Ghana in the last ten years. The risk of tuberculosis infection was low in the northern savannah zones compared to the southern coastal zones. Using a cut-off of 15 mm, the prevalence of infection ranged from 0.0% to 5.4% and the Annual Risks of Tuberculosis Infection 0.0% to 0.6%. There was an increase in the proportion of infected children after the age of 7 years. Children attending low and middle-class schools had a higher risk of infection than children attending upper-class schools.

Conclusion

Tuberculosis infection is still a public health problem in Ghana and to monitor the trend, the survey needs to be repeated at 5 years interval.

Background

Ghana is a West African country, bordering Burkina Faso to the north, Togo to the east, Cote d'Ivoire to the west and the Gulf of Guinea to the south. For administrative purposes, the country is divided into 10 regions and subdivided into 168 districts. Topographically, Ghana is divided into three ecological zones. The southern regions (Western, Central, Volta, Greater-Accra) make up the coastal zone, the central regions (Brong Ahafo, Ashanti, Eastern) the forest zone, and the northern regions (Upper-East, Upper-West, Northern) the savannah zone. Of the 22.5 million population of Ghana, 34% live in the southern coast, 48% in the central forest, and 18% in the northern savannah areas [1]. With estimated 46,693 new cases of all forms of tuberculosis (TB) in 2006, Ghana has the 15th highest burden in Africa [2].

The National Tuberculosis Control Programme (NTP) was established in 1994 to attempt among others to reduce the incidence and prevalence of TB in the country and the Directly Observed Therapy Shortcourse (DOTS) strategy was introduced the same year. DOTS coverage reached 100% in 2005 and 12,124 TB cases of which 7,505 were new smear positive were notified for an incidence rate of 55 and 34 per 100,000 respectively [2].

Using tuberculin survey to assess the extent of TB infection in Ghana has never been done since the establishment of the NTP. In 1957, a World Health Organization (WHO) sponsored study reported a point TB prevalence of 0.2% to 0.9% in the general population and 0.4% to 3% in the gold mining areas [3]. Surveys done in the late seventies in some urban areas estimated the prevalence of infection to be between 1% and 2% [4, 5].

These data are old and as disease reporting is also inadequate, there was an urgent need to establish recent risk of infection in Ghana and provide baseline data for the NTP.

This baseline tuberculin survey was therefore carried out to establish the recent risk of TB infection in different parts of Ghana. It was conducted in 2004 - 2006 among primary school children in eight regional capitals and their environs where Public-Private Mix (PPM) activities in TB control were to be implemented in response to a rapidly growing private health sector in the country, especially in cities. PPM activities aim to involve all health care providers - public and private as well as formal and informal in the provision of TB diagnosis and treatment according to international guidelines. The study population comprised school children because the annual risk of tuberculosis infection (ARTI) which is a measure for transmission of TB infection in the population is better calculated from the prevalence of infection estimated throughcross-sectional tuberculin surveys. ARTI estimates obtained from children reflect on relatively recent disease situation and its trends. In older age groups, higher prevalence of environmental mycobacteria and HIV infection may interfere with the interpretation of the survey results.

Methods

Study population

The study population comprised primary school children aged between 6 and 10 years from 21 districts in 8 out of 10 regions of Ghana namely; Greater-Accra, Ashanti, Eastern, Central, Western, Northern, Upper East and Upper West.

Sampling

A list of all primary schools in the eight regions was obtained from the Ghana Education Service. Schools in the regional capitals and its bordering districts were selected purposively to reflect the proportion of affluent private and free tuition public schools and small and large schools.

Training

Testers, readers and the other members of the tuberculin team received two weeks training in testing, reading, scar examination and other logistics of performing a tuberculin survey following international guidelines by Royal Netherlands Tuberculosis Foundation (KNCV) reference nurse before the start of the survey. The training was combined with a pilot survey.

Tuberculin test

A dose of tuberculin of 2 TU in 0.1 ml PPD RT23/Tween 80 from State Serum Institute (SSI) Copenhagen, batch number 1449A was used. Bacille Calmette-Guérin (BCG) vaccination status of each school child to be tested was assessed by physical examination for the presence or absence of a BCG scar. A dose of exactly 0.1 ml was slowly injected (intradermally-Mantoux technique) [6, 7]. In case of injury or scar on the left forearm, the test was given on right forearm and a note made in the comments column of the data form. The reaction to the test was read 72 hours after administration. If an induration was present its limits were determined and its largest transverse diameter measured in millimeters with a transparent flexible ruler of 15 cm [7, 8]. Each induration was assessed by one reader but when in doubt a reference reader was called to read.

Data management

The team leader verified completeness of the raw data on-site after each days' activity before being double entered into a data entry file - Microsoft Office Excel 2003 (Microsoft Excel, Palisade Corp, Newfield, NY, USA). Afterwards, the data files were compared to the raw data by one of the authors. Missing values, inconsistencies and outlier values were checked and corrected where necessary. Analysis of the data was done with SPSS version 15 (SPSS, Inc, Chicago, IL, USA).

Data analysis

Schools were classified as being situated in urban, peri-urban or rural areas and as upper, middle, or lower class. Age was reported as age in full years since the last birthday. Mean and median ages were calculated by adding 0.5 years to the reported age because on average the children are expected to be 6 months older than the age in full years. Differences in proportions were tested for statistical significance by the chi-square test.

We assessed whether there was a difference in the results in children with and without BCG scar. We also assessed whether terminal digit preference (tendency to round observations to numbers ending with zero or 5) was present by smoothing the data. This involves calculating the expected frequency at each millimeter (mm) of reaction as the average of three or five frequencies including one or two before and after the induration of interest [9].

Specific cut off levels (≥10 mm and ≥15 mm) were used to distinguish between infected and un-infected children. The mirror method which is based on the observation that the distribution of tuberculin reactions reflects two underlying distributions: that of reactions to TB infection and that of non-specific reactions was also used [1012]. It assumes that the tuberculin reactions among infected children are normally distributed around a mode of 16 to 17 mm and that there are no non-specific reactions larger than the mode. Indurations equal to the mode are counted once and all larger than the mode counted twice to obtain the estimated number of indurations. In our analyses we assumed the mode to be at 16 and 17 mm, as these values are used often in literature [12, 13].

Data was analysed per district to obtain estimates of TB infection and ARTI. The ARTI was calculated as 1 - (1-prevalence of infection)1/mean age [14].

The estimated ARTI is the average of the annual risks of infection experienced by the study sample from birth to the time of survey [15]. This risk may not have been constant over the period. Therefore, we assumed that the estimated ARTI corresponds closely to the mid-point of the average life of the individuals included in the survey.

Management of positive reactors

The NTP guidelines state that BCG vaccinated children with a Tuberculin Skin Test (TST) ≥ 15 mm and unvaccinated children with a TST ≥ 10 mm who are household contacts of a TB case and have symptoms of TB should be treated with anti-TB drugs. Children with TST ≥ 15 or 10 mm respectively, without a household contact but with symptoms of TB will be investigated further and treated for TB disease if necessary. During the survey, children with TST result of ≥ 15 mm for vaccinated and ≥ 10 mm for unvaccinated were therefore regarded as potentially infected and were referred to the local health facilities for further investigations.

Ethical considerations

The study was approved by the Scientific and Technical Committee and the Institutional Review Board, FederalWide Assurance 00001824 of the Noguchi Memorial Institute for Medical Research, Legon, Ghana in 2003 (reference number NMIMR-IRB CPN 022/02-03). Parents were requested to sign a written informed consent form. Only children that brought the signed informed consent form were included in the survey. Permission to enter the selected schools was sought from the Ministry of Education.

Results

Study population

The study covered children from 179 primary schools selected from a total of 338 schools in 21 districts in 8 out of 10 regions of Ghana. Children aged 6-10 years with consent form were 24,778. However, 23,600 (95.2%) were available for testing for which 21,861 (92.6%) were read (Table 1). The total number of eligible pupils per school was not registered, so the participation rate could not be calculated. However, from the experience of the field team, participation was nearly 100% in most public schools and much lower in some of the upper-class schools. The percentage of children whose tests were read varied from 74.1% to 99.2%. In districts with reading percentages below 90%, a national holiday, sports event, and rainy day were reasons for the low readings.
Table 1

Region, district, number of schools and children tested and read

Region

District

Total no of schools

No of schools selected

Children with informed consent

Children tested

% tested

Children read

% read

Eastern

New Juaben

40

28

3333

3279

98. 4

3051

93. 0

Central

AAK

5

2

496

457

92. 1

387

84. 7

 

Cape Coast

40

22

3125

3036

97. 2

2815

92. 7

 

KEEA

7

4

653

636

97. 4

621

97. 6

Northern

Savlegu-Nanton

7

4

699

643

92. 0

625

97. 2

 

Tamale

25

14

2285

2085

91. 2

1973

94. 6

 

T-K

15

7

756

705

93. 3

673

95. 5

Western

Ahanta-East

35

18

3005

2822

93. 9

2699

95. 6

 

Ahanta-West

5

3

808

777

96. 2

576

74. 1

 

Wassa-West

10

6

1033

987

95. 5

889

90. 0

Upper-East

Bolga

15

7

840

799

95. 1

765

95. 7

Upper-West

Wa

7

4

647

638

98. 6

622

97. 5

Ashanti

AN

8

4

255

250

98. 0

240

96. 0

 

BAK

6

3

389

385

99. 0

382

99. 2

 

Ejisu-Juaben

5

2

139

137

98. 6

133

97. 0

 

Kumasi

55

27

2815

2678

95. 1

2407

89. 9

Greater-Accra

Accra

15

6

990

959

96. 9

895

93. 3

 

Dangme-East

7

3

197

179

90. 9

169

94. 4

 

Dangme-West

10

5

586

538

91. 8

472

87. 7

 

Ga

15

7

1012

933

92. 2

848

90. 9

 

Tema

6

3

715

677

94. 7

619

91. 4

Total

 

338

179

24,778

23,600

95. 2

21,861

92. 6

AAK = Abura Asebu Kowmanse, KEEA = Komenda Edina Eguafo Abirem, T-K = Tolon-Kumbungu

AN = Atwima Nwobeagya, BAK = Bosumtwi Atwima Kwabianya

Age and sex distribution

The age distribution showed an increase in numbers of children towards older age: 11% were 6 years and 25%, 10 years. The proportion of girls was higher in all age groups (range 51.4% to 54.0%, p < 0.001).

BCG scar

BCG scar was visible in 89.3% of the children. It decreased with increasing age in all districts, the crude average increased from 87.1% in 10-year-olds to 92.5% in 6-year-olds, reflecting increasing BCG vaccination coverage in Ghana in the last ten years. The distribution of schoolchildren with BCG scar by age was similar in boys and girls, both in the total population (p = 0.31) and on the district level. The percentage of schoolchildren with BCG scar was highest in schools in urban areas (94.4%) and upper-class schools (92.2%).

TST reaction

No reaction was observed in 41.9% of those with and 49.1% of those without BCG scar (p < 0.01). The percentage of non-reactors was highest in the districts in the Ashanti region and lowest in the districts sampled from the Eastern and Central regions.

The distribution of reaction sizes is shown in Figure 1. As expected, the size of reaction was less than 5 mm in most children. However, the proportion of children with reaction less than 5 mm was less in those from Ashanti and Greater Accra regions which were surveyed first compared to the other six regions.
https://static-content.springer.com/image/art%3A10.1186%2F1471-2458-10-35/MediaObjects/12889_2009_Article_1946_Fig1_HTML.jpg
Figure 1

Distribution of tuberculin reaction sizes by region, in children with reaction size >0 mm.

The frequency distribution of reaction sizes >0 mm by BCG scar status is shown in Figure 2. There was no relevant effect of the presence of a BCG scar on tuberculin reaction size. The reaction sizes of all children were therefore used to estimate the prevalence of TB infection and the ARTI.
https://static-content.springer.com/image/art%3A10.1186%2F1471-2458-10-35/MediaObjects/12889_2009_Article_1946_Fig2_HTML.jpg
Figure 2

Distribution of the percentage of children with a reaction size >0 mm, and the cumulative percentage of children with a reaction size up to and including the size given on the x-axis, by BCG scar status.

ARTI

The frequency distribution of the reaction sizes showed digit preference at 10 and 15 mm. Using 5 point moving average seemed to provide the best correction of digit preference. Estimating the prevalence of infection using smoothed data did not show significant differences from the estimates based on the original data hence, the latter was used for the analysis.

The frequency distribution of the reaction sizes did not show a bimodal distribution. Therefore, it was not clear which method and cut-off point would provide the best estimate of the prevalence of TB infection and ARTI. In view of this, we resorted to the often used cut-off points of 16 and 17 mm.

Additional file 1, Tables S2 and S3 show the prevalence of infection and ARTI in the districts calculated using different methods. Using cut-off of 10 mm produced estimates for the prevalence of infection and ARTI which were different from those obtained using cut-off of 15 mm and the mirror method at 16 or 17 mm. If we assume that a cut of 10 mm overestimates the prevalence of infection and ARTI (3.3% to 18.8% and 0.4% to 2.4% respectively), we can assume that the other methods will probably reflect the range in which the best estimate of the prevalence of infection and ARTI will lie within the districts. Using a cut-off of 15 mm the prevalence of infection ranged from 0.0% to 5.4% and ARTI from 0.0% to 0.6% respectively. The risk of TB infection was lowest in the districts sampled from northern savannah and highest in districts sampled from southern coastal zone.

Figure 3 shows a consistent increase in the prevalence of infection with age after the age of seven years, regardless of which method was used. This did not change when the data was stratified with the presence or absence of BCG scar (data not shown).
https://static-content.springer.com/image/art%3A10.1186%2F1471-2458-10-35/MediaObjects/12889_2009_Article_1946_Fig3_HTML.jpg
Figure 3

Prevalence of infection by age, as estimated by using different methods.

Figure 4 shows a positive correlation between the estimated prevalence of infection and ARTI and the notification rates from each region.
https://static-content.springer.com/image/art%3A10.1186%2F1471-2458-10-35/MediaObjects/12889_2009_Article_1946_Fig4_HTML.jpg
Figure 4

Relationship between regional notification rate (per 100,000 inhabitants, 2000-2002) and the annual risk of TB infection (ARTI) per district, as estimated by using a cut-off point of 15 mm. District notification rates were not available therefore regional rates were used.

Discussion

Tuberculin surveys have some general limitations: a) schools are usually the point of entry and children not at school are likely to have a higher risk of TB because they tend to come from lower socio-economic classes [16]. Although there are no exact figures on school attendance in Ghana, it is assumed to be high. However, we observed a lower attendance in 6- and 7-year-olds compared to 8- to 10-year-olds and in rural compared to urban areas. Especially in these groups, the obtained estimates for risk of TB infection may be an underestimation; b) BCG scars are usually taken as proxy for BCG vaccination status. As children vaccinated at birth may not develop a scar, vaccination coverage was probably higher than the proportion of children with BCG scar observed in this survey (89.3%).

Other limitations identified were related mostly to sampling in this survey. Firstly, the districts sampled were from the capital cities and surrounding districts of the eight regions where PPM activities were being implemented. Therefore, they are not fully representative of all districts in the regions. No regional or national estimates of the risk of infection can be deduced from these data, only district estimates. Secondly, schools were not sampled randomly within districts. However, they were selected with care to obtain representative selection of schools within the district so we assume that this will not have introduced considerable bias. Thirdly, the characteristics of children who did not take part in the study because parental consent was not given was not determined. We therefore could not determine whether they were different from those studied. Fourthly, the number of children included in some districts was relatively small, making estimates for the risk of infection imprecise. Lastly, no bimodal distribution of reaction sizes was visible. Therefore, it was not possible to distinguish infected children from uninfected children and we estimated the prevalence of infection and ARTI by different methods to obtain a plausible range for these estimates. In this study, as also found in Tanzania [17], applying cut-off of 10 mm overestimated the ARTI. This may be due to limited specificity with this cut-off as a result of high prevalence of infections with non-tuberculous mycobacteria (NTM) [1719]. Despite its limitations, many useful results have become available through this survey. The risk of infection was lowest in the sparsely populated northern savannah and highest in the more populous southern coastal zones of the country an indication that control activities would have to focus more on the latter. There was a clear increase in the proportion of infected children by age after 7 years. Children attending low and middle-class schools had a higher risk of infection than children attending upper-class schools (data not shown). This is consistent with the theory that socio-economic status is an important determinant for TB infection and disease [16]. Unfortunately, it is not possible to extrapolate ARTI to TB incidence as the Styblo rule which states that "an annual incidence of 50 sputum-smear positive TB cases in a population of 100,000 generates ARTI of 1%" is not applicable in DOTS settings [20]. However, there was a clear correlation between estimated prevalence of infection and ARTI on the one hand and the notification rates on the other. All districts in Greater Accra except Dangme-East had higher ARTI than expected based on notification rates. This may indicate that case detection rates are lower in the Greater Accra region than in most other districts sampled. In New Juaben, the only district selected in the Eastern region, a lower ARTI was observed than expected based on this association. However, as this concerns only one district, it is unclear whether this is a reflection of high case detection rates in this region. Wassa west is part of the mining region where high ARTI was observed in the 1950's [3]. However, in this survey, ARTI does not seem to be particularly high compared to other districts in the country.

Besides results on infection pattern, other interesting results emerged from the survey. The percentage of children with BCG scar decreased with age, reflecting an increased uptake of BCG in the last decennium. However, inequality in BCG coverage does exist as the percentage of children with BCG scar was highest in pupils visiting upper-class schools, and the overall proportion of children with BCG scar varied between districts (data not shown). These differences did not affect ARTI estimates as BCG vaccination had minimal effect on reaction sizes greater than 10 mm, which are most relevant for determining the prevalence of infection [16].

We do not know why the distribution of non-reactors and reaction sizes varied between districts. A distribution with a higher proportion of lower reaction sizes is expected when cross-reaction to NTM are present. Unfortunately, data on national/regional prevalence of NTM in Ghana to relate to the distribution of reaction sizes is not available.

Conclusion

In conclusion, the survey has provided useful information to the NTP on TB transmission in Ghana and has helped to evaluate the programme performance. The positive correlation between the estimated prevalence of infection and ARTI and the notification rates from the regions had shown that the programme is performing well. From the results, it is highly recommended to repeat the survey at 5 years interval with particular attention on: 1) using the same districts and schools as in the current survey in order to assess trends in ARTI. 2) additional districts and schools would have to be randomly selected to make the selection representative of a region and to obtain sufficient numbers of children per region to narrow the confidence interval. 3) registering the total number of eligible children per school in order to calculate the participation rate, age group and gender, and 4) conducting tuberculin testing in a group of TB patients to assess their reaction sizes, which can be used to estimate the mode to be used in the mirror method for estimating the prevalence of infection.

Declarations

Acknowledgements

The fieldwork for the tuberculin survey was supported by many individuals and organizations. We especially thank the Ministries of Education and Health for their support, the regional and district health and education officers, and the headmasters and teachers of the schools for assisting the field teams during testing and reading days. We are also grateful to the Global Fund Against HIV/AIDS, TB & Malaria and the Ghana Health Service for their financial support.

Authors’ Affiliations

(1)
Bacteriology Department, Noguchi Memorial Institute for Medical Research
(2)
Epidemiology Department, Noguchi Memorial Institute for Medical Research
(3)
Research Unit, KNCV Tuberculosis Foundation
(4)
Center for Infection and Immunity Amsterdam (CINIMA), Academic Medical Center, University of Amsterdam
(5)
Department of Medicine, University of Ghana Medical School
(6)
Epidemiology Unit, National Tuberculosis Control Programme, Korle-Bu

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  21. Pre-publication history

    1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2458/10/35/prepub

Copyright

© Addo et al; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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