info@aditum.org    +1(205)-633 44 24

Knowledge, Attitude And Practice Regarding Pulmonary Tuberculosis As An Occupational Health Disease Among Miners At Neelkanth In Ndola, Zambia

Authors

Niza Rean Simwanza
The Copperbelt University School Of Graduate Studies Micheal Chilufya Sata School Of Medicine.

Article Information

*Corresponding author: Niza Rean Simwanza, The Copperbelt University School Of Graduate Studies Micheal Chilufya Sata School Of Medicine.

Received: March 09, 2025
Accepted: April 24, 2025
Published: May 04, 2025

Citation: Niza R Simwanza. (2025) “Knowledge, Attitude And Practice Regarding Pulmonary Tuberculosis As An Occupational Health Disease Among Miners At Neelkanth In Ndola, Zambia, Journal of International Research and Reviews. 1(1); DOI: 10.61148/JIRRS/003.
Copyright:  © 2025 Niza Rean Simwanza. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Introduction

Zambia is one of the many countries in sub-Saharan Africa that is burdened by tuberculosis (TB). Mine workers in Southern Africa including Zambia tend to have poor living and working conditions thereby having increased risk of TB and in addition working in the mines increases exposure to silica dust leading them to developing silicosis which increases their risk of developing PTB. Furthermore, ex-miners also tend to have an increased risk of TB due to previous exposure to silica dust.

The general objective of this study was to assess the knowledge, attitude and practice regarding TB as an occupational health disease among miners at Neelkanth mine in Ndola.

Methodology

This was a cross sectional study that assessed the Knowledge, Attitude and Practices of miners regarding TB as an occupational health disease. The study was conducted at Neelkanth mine in Bwana M’kubwa area, Ndola rural. Study participants were miners. The calculated sample size for the study was 384. A questionnaire was used to collect data from study participants. Data was entered and analysed using Spss version 16.0, Pearson chi squared test was performed and the output was then analysed further using multivariate logistic regression at 95% confidence interval.
Results
This study resulted in a total of 357 study participants instead of the calculated 384 that wereenrolled into the study, due to the fact that 27 questionnaires were incomplete and therefore eliminated from the study. The mean age was calculated to be 32.9 (standard deviation [SD]:7.4) years, with the majority of participants aged between 18-40years. Comparing the participants that could define TB to those that could not, those that could define were 1.84 times more likely to have good knowledge levels (CI95: 1.17, 2.91). Likewise, participants were 1.66 times more likely to know preventive measure of TB as an occupational health hazard compared to those who did not know (CI95: 1.18, 2.32). Participants who wear PPE were more than twice likely to protect themselves from TB compared to other study participants who did not (CI95: 1.25, 2.34). Participants who do not go for regular chest examination were more than twice likely to have TB compared to the study participants whodid not (CI95: 1.13, 2.11).

 
Conclusion

This study revealed through multivariate regression analysis of the results that there is a significant association between knowledge, attitude, practice and TB as an occupational health disease. These findings highlight the need for TB education amongst miners.
 


Keywords:

Introduction

Tuberculosis is an infectious disease caused by the bacteria Mycobacterium tuberculosis. The bacteria spreads through the air from person to person and mainly attacks the lungs, but it can affect other areas of the body [1]. The majority of people exposed to the bacteria do not experience tuberculosis symptoms right away [1]. Instead, the infection may go through three stages:

Primary TB Infection; this is when the bacteria first enter your body. In many people this causes no symptoms, but others may experience fever or pulmonary symptoms [2]. Most people with a healthy immune system will not develop any symptoms of infection, but in some people the bacteria may grow and develop into an active disease. Most primary TB infections are asymptomatic and followed by a latent TB infection [2].

Latent TB Infection; The bacteria are in your body and can be found through tests, but is not active. During this stage you do not experience symptoms and cannot spread the disease to others [3].

Active Disease; the TB bacteria are active and multiplying. You will feel sick and will be contagious. It is important to seek immediate treatment to avoid complications and infecting others [3].

 

Figure 1: shows Mycobacterium tuberculosis. Source; www.textbookofbacteriology.net

A third of the world's population is infected with Mycobacterium tuberculosis (MTB), and over 9 million new cases of tuberculosis (TB) are reported annually [4]. Treatment of drug- susceptible pulmonary TB is highly effective, with 85% (66 million cases) of reported cases estimated to have been successfully treated between 1995 and 2015 [4]. However, up to half of TB survivors have some form of persistent pulmonary dysfunction despite microbiologic cure [5-8]. Pulmonary dysfunction, ranging from minor abnormalities to severe breathlessness, can increase the risk of death from respiratory causes [9, 10].

Furthermore, treated TB patients appear to contribute substantially to the growing worldwide burden of chronic obstructive pulmonary disease (COPD) [9–10].

The symptoms of TB include a low-grade fever, night sweats, fatigue, unexplained weight loss of ten pounds or greater and a persistent cough [10]. Some people may not have obvious symptoms. Evidence of infection (a positive skin test) may occur from two to 10 weeks after exposure. The most hazardous period for developing TB disease is usually within six to 12 months after infection, but can be longer, occurring much later in life. [10].

The term ‘pneumoconiosis’ is used to describe a set of lung diseases caused by the repeated inhalation of small particles in which long-term retention in the lung is a key causative factor. [11]The site of damage within the lung is a function of both the size and the toxicity of the inhaled dust, fume or fibre. The ability of different types of particles to  cause  fibrosis  varies widely: crystalline silica is highly fibro genic, whereas iron oxide is not [11]. In susceptible individuals, pneumoconiosis usually develops after many years of exposure, sometimes presenting after retirement. [12] Where cases are detected during employment (e.g. during health surveillance), reduction or cessation of further exposures should be the goal. Prevention is of prime importance as the lung damage caused by pneumoconiosis is irreversible, and the retained substance may continue to cause harm many years after exposure has ceased [13].

According to the Occupational Health and Safety Institute, the regulatory body established under the Occupational Health and Safety Act, 2010, of Zambia [14], the weighted average of the incidence rate of PTB among current miners 1994–2014 was 658 per 100 000 populations. Figure 2 shows descriptive data of a sample of the incidence rate of PTB among current copper miners. The incidence rate increased from 1994 to 2005 but since 2005, it has steadily decreased. In 2014, the incidence rate of PTB among miners in Zambia was 288 per 100 000 populations.

 

Figure 2: Trends of PTB incidence among current copper miners based on Occupational Health and Safety Institute (Kitwe, Zambia) records review. Source; Tuberculosis in the mines of Zambia: A case for intervention by Pascalina Chanda-Kapata and colleagues.

The TB notification rate is the number of TB cases (new and relapse) notified to the national health authorities during a specified period of time per 100,000 populations [97]. The TB notification rate as reported by the Zambian Ministry of Health through the National TB Control Program may be used as an indicator to determine the magnitude of the burden of TB in a specific location [15]. The two main provinces where the mines are concentrated had the highest TB notification rates. The Copper Belt Province which holds the most copper mines in the region had a notification rate of 415 per 100 000 people in 2013 which was more than 10- fold the national TB notification rate [15].

Statement Of The Problem

The national prevalence survey showed the Copper Belt Province to have the highest prevalence of bacteriologically confirmed TB of 1211 per 100 000 people in the general population. Therefore, it was the aim of this research to explore the factors leading to this confirmed prevalence rate, in Ndola rural, Bwana Mkubwa area, the site of Neelkanth mine. This site became an area of interest to be considered for studies regarding TB, so as to determine the knowledge, attitude and practice about TB as an occupational health hazard among the said miners. The miners at this mine is that they are working without proper safety boots, work suite or aspirators during their long shifts and this prompted this study.

Justification

The key to controlling TB in the mining sector is primary prevention based on comprehensive population-wide programmes that teach people on the importance of proper protective equipment while they work as well as proper adherence to treatment if found with TB, this is very important for every miner to know.

It was observed when a visit to Neelkanth a mine that is mining lime and electric cables in Bwana Mkubwa area, revealed that the miners there work without the full proper protective gear that is needed in such an environment. This study is important because its findings will reveal how knowledgeable the miners are about TB, the attitude and practices that they do in order to avoid putting themselves at the risk of contracting TB. It will also provide information to relevant authorities like Ministry of Health and other authorities that are concerned about TB in the mining sector with the gaps that need attention both on the mine management side and miner’s side.

Literature Review Global Review

Global TB targets for the period 2016–2035 have been set as part of the United Nations (UN) Sustainable Development Goals (SDGs), the World Health Organization (WHO) End TB Strategy and the political declaration of the UN high-level meeting on TB held in 2018[17]. The End TB Strategy was adopted by all WHO Member States at the World Health Assembly in 2014 [18]. The political declaration of the UN high-level meeting on TB held in September 2018 [19] reaffirmed the SDG and End TB Strategy targets. It also established new targets for the numbers of people to be provided with TB treatment and TB preventive treatment during the period 2018–2022, which were derived from and consistent with End TB Strategy milestones; and new targets for the funding to be mobilized between 2018 and 2022, based on the Stop TB Partnership’s Global Plan to End TB [20]. Globally, the TB incidence rate is falling, but not fast enough to reach the first milestone of the End TB Strategy; that is, a 20% reduction between 2015 and 2020. Worldwide, the cumulative reduction from 2015 to 2019 was 9% (from 142 to 130 new cases per 100000 population), including a reduction of 2.3% between 2018 and 2019 [21].

A total of 78 countries are on track to reach the 2020 milestone. This includes seven high TB burden countries1that have already reached it (Cambodia, Ethiopia, Kenya, Namibia, the Russian Federation, South Africa and the United Republic of Tanzania) and three others that are on track (Lesotho, Myanmar and Zimbabwe) [22]. Worldwide, TB is the leading infectious disease killer and one of the top10 causes of death overall [23].

Globally, some of the main key risk factors of TB include; Bacillary Load-Epidemiological studies conducted during mid- 20th century have shown that smear positive cases are more infectious than the others [24-25]. An untreated sputum positive patient can infect approximately 10 individuals per year, and each smear positive case can lead to two new cases of TB, at least one of which will be infectious [26-27]. Proximity to an Infectious Case. Close contacts of infectious TB cases including household contacts and care givers/health care workers [28] area at higher risk of becoming infected with Mycobacterium tuberculosis and development of primary active tuberculosis. Diabetes; Diabetes has been shown to increase the risk of active TB disease [29, 30]. It is estimated that currently 70% of people with diabetes live in low- and middle-income countries [31], and the rates are steadily increasing in areas where TB is endemic, including India and sub- Saharan Africa [32].

Alcohol; Alcohol has been recognized as a strong risk factor for TB disease [33]. The harmful use of alcohol ranks among the top five risk factors for disease, disability, and death, as well as being a causal factor in more than 200 disease and injury conditions, including tuberculosis, worldwide [34]. It has been estimated that approximately 10% of all tuberculosis cases are attributable to alcohol use [35]. Malnutrition; Studies have shown that malnutrition (both micro- and macro-deficiency) increases the risk of TB because of an impaired immune response [36–38]. TB disease can itself lead to malnourishment because of decreasing appetite and changes in metabolic processes [39]. The association between malnutrition and TB has been shown with BCG vaccine trials performed in USA during the late 1960s estimating that malnourished children are twice as likely to contract TB disease as their appropriately nourished peers [40]. Indoor Air Pollution; in developing countries, the percentage usage of solid fuels for cooking is more than 80% [41]. Firewood or biomass smoke has been previously recognized as an independent risk factor for TB disease in case control studies conducted in India and Brazil [42– 44]. Illicit drug use; Epidemiological data suggest that the relationship between tuberculosis and illicit drug use is increasing, leading to a public health problem because it involves political, human, social, and economic aspects [45-46]. Smoking; it is estimated that, worldwide, 1.3 billion people consume tobacco and that most of them live in underdeveloped or developing countries, where the tuberculosis rates are also higher [47]. Therefore, the greatest impact of smoking in terms of public health issues related to infection is probably the increase in the risk of tuberculosis. Some systematic reviews and meta-analyses of observational studies have shown an unfavourable association between the global epidemics of tuberculosis and smoking, exposure to tobacco smoke having been associated with tuberculosis infection, active tuberculosis, and tuberculosis- related mortality [48-49].

Mineral mining is one of the world’s most hazardous occupations, not only because of the safety issues involved, but also because of the clear link between mining, lung disease and TB [84–86]. Mineral mining exposes workers to high levels of silica dust [87], which carries with it an increased risk of lung disease [88-89], such as silicosis. Like HIV, silicosis has been demonstrated to greatly increase the risk of TB, including active TB [84]. The impact of silicosis on health has been known since the late 19th century. Even without the presence of silicosis, silica exposure alone is associated with an increased lifelong risk of TB disease [84- 87]. Data from India [86], China [88, 90] and Japan [91] have indicated that coal mining and residing in communities near coal mines might carry an increased risk of TB. Rural mining communities and miners’ families are susceptible to TB because of the circular migration patterns of miners as they travel between mines and their home [85, 92].

The KAP study done in Southern Africa revealed that; Knowledge on TB was universal across the ten SADC countries as 100% of the participants in the study, regardless of employment category, had received information on TB [98]. However, only 78% of the participants reported that they were aware of the main sources of TB information. This awareness ranged from 53% in Zimbabwe to 92% in Mozambique [98]. Compassion towards people with TB was high, with 78% of the respondents at regional level feeling that they would feel compassionate towards people with TB [98]. The data show very good health seeking behaviour with about 98% reporting that they would visit a health facility if they are found to have TB. There is minimal variability between countries and population types [98].

Africa Review

In Africa, tuberculosis is often the first manifestation of HIV infection, and it is the leading cause of death among HIV-infected patients [50–54]. In hospital-based series, 40–65% of HIV-infected African patients with respiratory disease had tuberculosis [24-26]. In primary health and chest clinic settings, tuberculosis was confirmed in 43–70% of adults with cough for 3 weeks or longer (chronic cough) in Zimbabwe, Kenya, and Malawi [30-31].

Figure 3: showing number of people provided with TB treatment. Source; global community report

Patients with tuberculosis now commonly present with atypical symptoms: MTB was isolated from 9% of adults with acute pneumonia in Kenya [32], 35% of people with cough for less than 3 weeks in Malawi [33] and 23% of febrile HIV-infected inpatients in Tanzania [34] and 13% of HIV-infected patients with chronic diarrhoea in Kenya [35].

In Africa, the following are some of the risk factors of TB in the mining sector. Poor living and working conditions further that exacerbate the risk for TB. A significant number of miners are migrants, traveling between their rural home areas and densely populated mining communities. More than 100,000 workers in the mining industry in South Africa come from Lesotho, Swaziland, Mozambique, or Botswana, and approximately 80 percent are concentrated in the gold mining industry (76). Deep-level gold mine shafts are often only two to three meters wide and can reach up to several kilometres underground (77). This makes crucial TB preventative strategies, such as air circulation and ventilation aimed at reducing silica dust, extremely difficult to implement, particularly in the cramped confines at the rock face [77]. Personal protection equipment, required to enter the mine shaft, is little used in practice because of poor enforcement and because workers often remove the equipment as a result of the increased difficulty breathing in a hot, sweaty environment (73). In part because of these conditions, it is estimated that 89 percent of miners are latently infected with TB (74). These individuals collectively represent a large population of individuals who develop active TB. Not only are rates of new TB infections high, but the rate of recurrent TB infection in the gold mining industry, whether or not complicated by silicosis, is more than twice the rate in the general population. Charalambous and colleagues showed that among 609 gold mine workers followed for a median of 1.02 years after a first cured episode of TB, 57 developed recurrent disease. Re-infection was demonstrated by genotyping in 69 percent of those with isolates recovered from both the first and subsequent TB episodes (80–82).

KAP studies done in Ethiopia revealed that; among the participants, 345 (83%) had heard information about TB [99] and One hundred seventy (41%) of participants responded the mode of transmission as through the air when a person with TB sneezes or cough, the majority (82%) said TB can be transmitted from person to person [99]. The majority (70%) of participants responded that its transmission is not preventable, while 92 (22.4%) replayed that covering the mouth and nose while coughing or sneezing is a possible method to prevent the transmissions [99]. The majority of participants (29%) considered TB as not very serious [99] and re than three-fourth (82%) of participants were have not received any health education about TB and 352 (85%) respondents did not take care during coughing or sneezing [99]. In Tanzania, study participant scoring at least 60% of the possible maximum scores was considered as having a good knowledge, positive attitude or good practices. And herein, a participant having positive TB attitude would mean they acknowledge TB exist, recognizes its impact on health and would seek or advise TB-infected individuals to seek the correct remedies [100].

National Review

Zambia is one of the many countries in sub-Saharan Africa that is burdened by tuberculosis (TB). The recent Zambia National TB Prevalence Survey 2013–2014 estimated the prevalence rate of all forms of bacteriologically confirmed pulmonary TB (PTB) among those aged 15 years and above to be at 638 per 100 000 populations which is higher than the prevalence rate in high TB burden countries such as Pakistan and Nigeria [37].

Approximately 70% of people with TB in Zambia are also co- infected with HIV [38]. According to the Zambia Demographic and Health Survey 2013–2014, the prevalence of HIV was estimated to be 13.5% in Zambia [39]. Before the HIV/AIDS epidemic in Zambia, the case notification rate of TB in Zambia in 1985 was 124 per 100 000 but the increasing HIV/AIDS epidemic in the period between 1990 and 2000 may have contributed to the increase of case notification rate to 512 per 100 000 as captured from routine facility based records countrywide [40]. The implementation of direct observed treatment short course and the TB/HIV collaborative control activities have contributed to a slight decline of TB [38].

However, the disease still remains a public health problem in Zambia [41-42]. TB being an airborne disease entails that enclosed areas such as mining sites with poor ventilation create favourable environments for TB transmission [43-44]. TB is one of the main health risks which have been found to be associated with mining [45].

Mine workers in Southern Africa including Zambia tend to have poor living and working conditions thereby having increased risk of TB and in addition working in the mines increases exposure to silica dust leading them to developing silicosis which increases their risk of developing PTB [93]. In addition, ex-miners also tend to have an increased risk of TB due to previous exposure to silica dust [47].

Underground mining produces dust, noise and in some mine sections heat and gases, such as sulphur dioxide. Workers also face risks of pneumoconiosis due to poor ventilation, and of rock falls causing injuries that may be fatal. These mines also raise the risk of contamination of water from the chemicals used in processing the minerals and acid mine drainage. These conditions were recorded in Nkana underground mine [93].

KAP studies on TB in the mines of Zambia proved to be scarce [17], however, other similar studies regarding TB in the mines were considered in this literature review as stated above

General Objective

To assess the knowledge, attitude and practice regarding TB as an occupational health disease among miners at Neelkanth mine in Ndola.

 

Specific Objectives
1.    To determine the knowledge levels among Neelkanth miners regarding TB as an occupational health disease.
2.    To determine the attitude among Neelkanth miners regarding TB as an occupational health disease.
3.    To assess the practices among Neelkanth miners regarding TB as an occupational health disease.

Research Questions
1.    What are the knowledge levels among the Neelkanth miners regarding TB as an occupational health disease?
2.    What is the attitude among Neelkanth miners regarding TB as an occupational health disease?
3.    What practice is among the Neelkanth miners regarding TB as an occupational health disease?

Methodology Study Site
This study was conducted at Neelkanth mine in Bwana Mkubwa area, this is an open pit mine in Ndola rural, copper belt province, Zambia. Neelkanth lime limited is located along Chilengwe Road, Southern extension of the Copper belt province, east of the T3 highway.
This mine mines lime, lime related products and electric cables. The population of the miners is over 500.
Target Population
The target population was the miners both female and male aged 18 years and above. This target population was chosen due to the fact that the miners are aged 18years and above.
Study Design
This was a cross sectional study that used a structured questionnaire to collect data from the study participants.
Sample Size
The following formula was used to determine the required sample size using the Statical programme in Epi Info version 7.
n
Sample size =      
n
1 +      Population size

P (1-P)
Where    n = Z2       
e2

Total Population Size

118,464

Level of Confidence Measure

1.96 (at 95% Confidence level)

Margin of Error (MOE)

5%

Baseline levels of the indicators

50% (as no estimates exist)

Number of age/sex Estimates

18 years and above

Design effect (Deff)

2.00 (as no information on previous surveys is available)

Sample size

384

n = Sample size, Z = critical value of the normal distribution at required confidence level, p = sample proportion, e = margin of error

Table I: showing sample size determination

Sampling Procedure
The survey sample is the set of survey participants selected from the larger survey population. The survey sampling determined how participants were selected and addressed the generalizability, certainty, and precision of results by defining who is included in the survey and how many people were needed.
In this study, the simple random sampling technique was used.
Inclusion And Exclusion Criteria
The inclusion criteria:
1.    All male/female miners in specific job roles such as crushing, blasting or breaking (roles directly involved in dust) are eligible to participate in this study.
2.    All miners willing to give consent The exclusion criteria:
1.    Miners in administrative works (office based roles) will not be included in the study.
2.    Miners not willing to give informed consent
 
Data Collection And Analysis
Three research assistants were recruited to collect the data. These were supervised by the Principal investigator. A paper questionnaire was used to elicit responses from the interviewees. This investigator and the research assistants went to the site of the mine and physically interview the participants. The investigators explained the objectives of the study to the miners. Written informed consent was obtained from each miner before being enrolled into the study. The questionnaire covering aspects of knowledge, attitude, and practice about TB as an occupational hazard were administered by the investigators to the study participants. The data was entered and analysed in Spss version 16.0. The collected data was analysed using the chi square test and multivariate logistic regression at 95% confidence level.
The questionnaire was divided into the following sections: interviewer name, information on knowledge, attitudes, and practices about TB. See Appendix 2.

Ethical Considerations
Ethical clearance for the study was obtained from the Tropical Diseases Research Centre (TDRC) ethics review committee and the National Health Research Ethics Committee (NHRC). Written Informed Consent was obtained from each study participant before being enrolled into the study. Confidentiality of information was observed.
Results
Demographic characteristics about study participants
A total of 384 participants were enrolled into the study but 27 questionnaires were incomplete and this resulted into the sample size being reduced to 357. Table 1 shows a summary of demographic characteristics about the study participants. Table 1 further shows that they were more male than female participants in the study with a ratio of 1.3:1. The mean age was calculated to be 32.9 (standard deviation [SD]: 7.4) years, with more than half of the participants aged between 18-40years. More than three quarters (82.9%) of the study participants were from households that had 1-7 occupants per household. More than half (65.5%) of the study participants had children between the ages 0-7. The majority of the participants (38.4%) had attained primary school education.
Table 1: Demographic Characteristics About Study Participants

Variable

Frequency

Percentage (%)

Age groups           18-30

31-40

41-50

156

134

67

43.7

37.5

18.8

Sex                     Male

Female

202

155

56.6

43.4

Number of occupants per household

1-7 people

8-15 people

 

296

61

 

82.9

17.1

Number of children per household

0-7 years

8-17 years

 

234

123

 

65.5

34.5

Level of education attained

None Primary Secondary

Completed secondary/higher

Refused to comment

 

45

137

107

55

13

 

12.6

38.4

30.0

15.4

3.6

Table 2: Study Participants’ Response To Knowledge About Tb As An Occupational Health Disease

Question

Frequency

Percentage (%)

What is TB?        Can define

Can’t define

257

100

72.0

28.0

Do you know what causes TB?

I know

I don’t know

 

208

149

 

58.3

41.7

What do you think causes TB?

Smoking Exposure to silica dust

Close to an infected person Working without PPE

I do not know

 

71

49

76

12

149

 

19.9

13.7

21.2

3.4

41.7

Among the listed risk factors below, what do you think causes TB?

Crowed places Exposure to silica dust

Close contact to the infected Working without PPE Poor ventilation at work

 

 

34

153

93

39

38

 

 

9.5

42.9

26.1

10.9

10.6

Is TB preventable?                   Yes

No

199

158

55.7

44.3

Do you know how to protect yourself from TB?                                  Yes

No

 

186

171

 

52.1

47.9

Do you know the sign and symptoms of TB?                                              Yes

No

 

247

110

 

69.2

30.8

Can anyone get TB?                    Yes

No

252

105

70.6

29.4

Is TB curable?                           Yes

No

290

67

81.2

18.8

Is it important to finish TB treatment?

Yes No

 

249

108

 

69.7

30.3

Extent of knowing TB            Extensively

Little Nothing

75

184

98

21.0

51.5

27.5

Table 2 shows study participants` response to knowledge about TB as an occupational health disease. The participants’ knowledge about TB etiology, prevention, protection, transmission and treatment as an occupational health disease is presented in Table 2. More than half (72%) of the participants’ had knowledge concerning definition, causes, risk factors and prevention (55.7%) of TB as an occupational health disease. The majority of the participants (70.6%) knew that anyone could get TB and 81.2% knew that TB can be cured. More than half (52.1%) knew how to protect themselves from TB and that it is important to finish TB treatment.
Table 3: Study Participants’ Response To Questions On Attitude About Tb As An Occupational Health Disease

Question

Frequency

Percentage (%)

Is TB preventable in the mines?

Yes No

 

171

186

 

47.9

52.1

Do you think working in the mine increases the chance of contracting TB?

Yes No

 

 

191

166

 

 

53.5

46.5

Would you work closely with a colleague who has TB?                 Yes

No

 

81

276

 

22.7

77.3

Should a colleague with TB be allowed to come for work?                        Yes

No

 

122

235

 

34.2

65.8

What would be your reaction if your closest colleague suffers from TB?

Not discriminate Discriminate

 

 

204

153

 

 

57.1

42.9

Who do you think is responsible for preventing TB in the mines?

Management Miners

Both

 

 

187

80

90

 

 

51.8

22.4

25.2

What should a miner do if fired from work because they have contracted TB?

Report No report

 

 

132

225

 

 

37.0

63.0

Table 3 shows study participants` response to questions on attitude about TB as an occupational health disease. Table 3 further shows that more than half (52.1%) of the participants said TB as an occupational health disease is not preventable in the mines and that working in the mine increases the risk of contracting TB. Two-thirds (77.3%) of the participants said they would not work closely with a colleague infected with TB and that a colleague with TB should not be allowed to come for work. More than half (57.1%) of the study participants would not discriminate a closest colleague who contracted TB and more than half (51.8%) of the participants said it is the responsibility of the mine management to prevent TB in the mine. More than half (63.0%) of the study participants said they would not report if they were fired because they contracted TB.
Table 4: Study Participants’ Response To Questions On Practice About Tb As An Occupational Health Disease

Question

Frequency

Percentage (%)

Do you know how to protect yourself from TB?

I know I don’t know

 

 

186

171

 

 

52.1

47.9

Do you wear PPE?    Yes

No

247

110

69.2

30.8

Do you go for regular chest examinations?

Yes No

 

 

131

226

 

 

36.7

63.3

Why do you do regular chest checkups?

Important Not important

 

 

229

128

 

 

63.4

35.5

Were you screened for TB at the time of being employed as a miner?

Yes No

 

 

198

159

 

 

54.8

44.0

Table 4 shows study participants` response to questions on practice about TB as an occupational health disease. Table 4 further shows that more than half (52.1%) of the study participants knew how to protect themselves from TB as an occupational health disease and almost two-thirds (69.2%) of the participant’s wear PPE as they work. More than half (63.3%) of the study participants do not go for regular chest examinations and more than half (63.4%) of the participants know that it is important to go for regular chest checkups. More than half (54.8%) of the study participants were screened for TB at the time of employment. The difference of practice levels about TB as an occupational health hazard and sex (male/female) was good (52.1%).
Table 5: Association Between Study Participants’ Demographic Characteristics And Awareness Of Tb As An Occupational Health Disease

 

Awareness of TB as an

Occupational health disease

 

Yes

No

 

Variable

n(%)

n(%)

P value

Age groups

18-30yrs 31-40yrs

41-50yrs

30(49.2)

28(45.9)

3(4.9)

94(31.8)

128(43.2)

74(25.0)

0.001

Sex

Male

Female

22(36.1)

39(63.9)

180(60.8)

116(39.2)

<0.001

House groups

1-7people

8-15people

34(55.7)

27(44.3)

170(57.4)

126(42.6)

0.808

Children groups

0-7yrs

8-17yrs

56(91.8)

5(8.2)

266(89.9)

30(10.1)

0.643

Level of education                      none Primary Secondary

Completed secondary/higher Refused to comment

6(9.8)

24(39.3)

22(36.1)

9(14.8)

0(0.0)

39(13.2)

113(38.2)

85(28.7)

46(15.5)

13(4.4)

0.396

Table 5 shows the association between demographic characteristics of study participants and awareness of TB as an occupational health disease. There was a statistically significant association between participants age groups and awareness of TB as an occupational health disease with (P<0.05). There was also a positive significant association between sex and TB as an occupational health disease with (P<0.05).
 
Table 6: Association Between Knowledge Levels And Tb As An Occupational Health Disease

 

TB As an occupational health

disease

 

Yes

No

 

Variable

n(%)

n(%)

P value

What is TB?

Yes

No

55(90.2)

6(9.8)

202(68.2)

94(31.8)

0.001

What Causes TB?

Yes

No

45(73.8)

16(26.2)

163(55.1)

133(44.9)

0.007

Risks factors of TB?        Crowed places

Exposure to dust Close to infected person

Without PPE Poor ventilation

9(14.8)

30(49.2)

10(16.4)

7(11.5)

5(8.2)

25(8.4)

123(41.6)

83(28.0)

32(10.8)

33(11.1)

0.209

Is TB Preventable?

Yes

No

39(63.9)

22(36.1)

160(54.1)

136(45.9)

0.157

Do you know how to Protect yourself?

Yes No

 

37(60.7)

24(39.3)

 

149(50.3)

147(49.7)

 

0.142

Do you know sign and symptoms of TB?

Yes No

 

47(77.0)

14(23.0)

 

200(67.6)

96(32.4)

 

0.144

Can anyone Get TB?

Yes

No

53(86.9)

8(13.1)

199(67.2)

97(32.8)

0.002

Is TB curable?

Yes

No

59(96.7)

2(3.3)

231(78.0)

65(22.0)

0.001

Finishing TB treatment important?     Yes

No

45(73.8)

16(26.2)

204(68.9)

92(31.1)

0.453

Table 6 shows the association between knowledge levels and TB as an occupational health disease. Table 6 also shows that, there was a positive significant association between what is TB and TB as an occupational health disease with a (P<0.05). Table 6 further shows that there was a positive significant association between what causes TB and TB as an occupational health disease with a (P<0.05). There was also a positive significant association between can anyone get TB and TB as an occupational health disease with a (P<0.05). Lastly, there was a positive association between is TB curable and TB as an occupational health disease with (P<0.05).
 Table 7: Association Between Attitude Levels And Tb As An Occupational Health Disease

 

TB As An Occupational Health Disease

 

Yes

No

 

Variable

N (%)

N (%)

P value

Is TB Preventable in mines?

Yes No

 

46(75.4)

15(24.6)

 

125(42.2)

171(57.8)

 

<0.001

Working in the mine increases risk of Contracting TB?                   Yes

No

 

31(50.8)

30(49.2)

 

160(54.1)

136(45.9)

 

0.645

Would you work closely with colleague who has TB?

Yes No

 

 

28(45.9)

33(54.1)

 

 

53(17.9)

243(82.1)

 

 

<0.001

Should infected workers be allowed to work?                    Yes

No

 

33(54.1)

28(45.9)

 

89(30.1)

207(69.9)

 

<0.001

Would you discrimate infected colleagues?                             Yes

No

 

36(59.0)

25(41.0)

 

168(56.8)

128(43.2)

 

0.745

Who is Responsible for prevention of TB in mines?                                  Management

Miners Both

 

43(70.5)

5(8.2)

13(21.3)

 

144(48.6)

75(25.3)

77(26.0)

 

0.003

If fired due to TB, would you report?

Yes No

 

30(49.2)

31(50.8)

 

102(34.5)

194(65.5)

 

<0.001

Table 7 shows the association between attitude levels and TB as an occupational health disease. Table 7 shows that there was a positive significant association between is TB preventable in mines and TB as an occupational health disease with a (P<0.05). There was a positive significant association between would you work closely with colleague who has TB and TB as an occupational health disease with a (P<0.05). Should infected workers be allowed to work and TB as an occupational health disease showed a positive significant association with a (P<0.05). There was a positive significant association between who is responsible for prevention of TB in mines and TB as an occupational health disease with a (P<0.05). Lastly, there was a positive significant association between if fired due to TB would you report and TB as an occupational health disease with a (P<0.05).
Table 8: Association Between Practice Levels And Tb As An Occupational Health Disease

 

TB As An Occupational Health Disease

 

Yes

No

 

Variable

N (%)

N (%)

P value

Do you know how to protect yourself from TB?                                           Yes

No

 

37(60.7)

24(39.3)

 

149(50.3)

147(49.7)

 

0.142

Do you wear PPE?                                           Yes

No

47(77.0)

14(23.0)

200(67.6)

96(32.4)

0.144

Do you go for chest exam?                                               Yes

No

38(62.3)

23(37.7)

93(31.4)

203(68.6)

<0.001

Are checkups important?                                               Yes

No

21(34.4)

40(65.6)

119(40.2)

177(59.8)

0.400

Were you Screened?                                               Yes

No

24(39.3)

37(60.7)

114(38.5)

182(61.5)

0.903

Table 8 shows the association between practice levels and TB as an occupational health disease. The table shows that, there was a positive significant association between the study participants that do go for regular chest exams and TB as an occupational health disease with a (P<0.05). The table also shows that there was no significant association between participants who did not know how to protect themselves from TB and TB as an occupational health disease with a (P>0.05).
Table 9: Multivariate Logistic Regression Output And Association To Tb As An Occupational Health Disease

Question

AOR

95% CI

What is TB?                                                                          Yes

No

1.84

1

1.17,2.91

Is TB Preventable in the mines?                                                                           Yes

No

1.66

1

1.18,2.32

Do you wear PPE?                                                                          Yes

No

1.71

2

1.25,2.34

Do you go for regular chest exam?                                                                           Yes

No

1.55

2

1.13,2.11

Table 9 shows multivariate logistic regression output and association to TB as an occupational health disease. The table shows results of multivariate logistic regression analysis of four variables that had an independent and statistically significant association to TB as an occupational health disease. Comparing the participants that could define TB as an occupational health disease to those that could not, those that could define were 1.84 times (CI95: 1.17, 2.91) more likely to define. Likewise, participants were 1.66 times (CI95: 1.18, 2.32) more likely to know preventive measure of TB as an occupational health disease compared to those who did not know. Participants who wear PPE wear more than twice (CI95: 1.25, 2.34) likely to protect themselves from TB compared to their counterparts who did not. Participants who did not go for regular chest examination were twice (CI95: 1.13, 2.11) more likely to have TB compared to the counter parts who did not.
Discussion
This study assessed the knowledge, attitude and practices about pulmonary Tuberculosis as an occupational health disease at Neelkanth mine in Ndola, Zambia. In terms of knowledge, the majority (72%) of the study participants knew what TB is and this is below the findings in a similar study done in the mines on the Copperbelt and North Western provinces of Zambia
[101] in which a 94% knowledge level was recorded. This difference shows that there is need for TB education among Neelkanth miners.
It was revealed in this study that more than half (53.5%) of the respondents indicated that working in the mine increases the risk of one contracting TB due to the fact that the mine provides little to no PPE and also the miners themselves do take off aspirators due to the fact that the environment they work in has poor air circulation and ventilation, this is consist with other studies that were done in South Africa [73]. Our research also revealed that two-thirds of miners stigmatise against TB infected colleagues and would not want to work closely with them. This is consistent in the research that was conducted in other Zambian mines [93] in which it was found that the majority of miners would not disclose to their supervisor over a TB diagnosis for fear of job loss.
Our study also showed that more than half of the respondents had not suffered from TB since joining this mine, this is consistent with studies done in other mines in Zambia [101] in which it was found that less than half of the respondents had tested positive for TB [101]. It was also observed that more than half of the miners at this mine did not go for regular chest examination this may be due to the fact that the mine does not cover the costs of regular chest examinations and this does not help the miners as exposure to silica dust has been associated with TB. Silica-related TB is a serious condition since the risk of TB is life-long even after exposure ceases [96].
There was limited data and research in Zambia to aid in fully determining the burden of TB in the mines and the risk factors associated with it. However, the few studies and data available show that TB is a significant health problem among miners in Zambia [93].
The implications of this study findings include, the fact that this study was only done at one mine, it may not be a representation of all Zambian mines and therefore, these findings cannot be generalised to include all mines in Zambia. Although, the research assistants were trained to assist in data collection, we cannot rule out the possibility of social desirability bias. Due to the literacy levels among our study participants, the research assistants had to read and explain in a local language to some of the participants for them to understand what the question was asking, in spite of the merits, one of the disadvantages is the possibility of having the interviewer effects leading to the interviewer bias.

Study Limitations
The study design provided reliable, valid information with a few limitations such as, miners were not coming out freely in the open to admit that they have TB or have had TB for fear of being discriminated, stigmatised and dismissed from work as the mines do not want to be liable for their health. Some Participants were not finishing answering the whole questionnaire and this affected the overall sample size and reduced it from 384 to 357.
Recommendation
Based on the findings of this research, it is cardinal for mines to consider TB education workshops once in a while for its miners. Also TB flyers and posters can be hanged within the mine premise to raise awareness.
There is also need for government through the ministry of mines and mineral development to strengthen laws against mines that are operating with miners who are not provided with full proper PPE, pre-chest examinations and regular chest examinations. This will greatly help in the reduction of TB in the mining sector.
The occupational Health and Safety Institute is the institute responsible for ensuring that all workers and former workers in industries including miners and former miners regularly and routinely screened for occupation health diseases including TB. It is therefore, very cardinal for this branch of government to run effectively and without bias in ensuring the miners are properly screened for occupational health disease (TB) and recommend all miners found to be sick to worker’s compensation union. We strongly recommend that the worker’s compensation union advocate for miners who have completed TB treatment and are fit to work to come back to their respective mine. This will encourage other miners to routinely go for check-ups and not to be afraid of the outcome should they be found with PTB or silica- related TB.

Conclusion
The study revealed that the knowledge levels were good, however, this was not effectively seen in their attitude and practice levels as these were lower than the knowledge level. This study also revealed that there is a significant association between knowledge, attitude, practice and TB as an occupational health disease. These findings highlight the need for TB education among miners.
List of Abbreviations

COPD    chronic obstructive pulmonary disease
HIV    Human immune deficiency virus
MTB    Mycobacterium tuberculosis
PTB    Pulmonary Tuberculosis
SDG    Sustainable development goals
SSA    Sub Saharan Africa
TB    Tuberculosis
TDRC    Tropical disease research centre
UN    United Nations
WHO    World Health Organisation

 

References

  1. American Thoracic Society and CDC. Diagnostic standards and classification of tuberculosis in adults and children. Am J Respir Crit Care Med 2000; 161 (4): 1376– 1395. 
  2. American Thoracic Society and Infectious Diseases Society of America. Diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med 2007; 175: 367–416.
  3. CDC. Controlling tuberculosis in the United States: Recommendations from the American Thoracic Society, CDC, and the Infectious Diseases Society of America. MMWR 2005; 54 (No. RR-12). World Health Organization. Global Tuberculosis Report 2015. 20th edition. Geneva, WHO, 2015. Google Scholar
  4. Hnizdo E, Singh T, Churchyard G, Chronic pulmonary function impairment caused by initial and recurrent pulmonary tuberculosis following treatment. Thorax 2000; 55: 32–38. 
  5. Plit ML, Anderson R, Van Rensburg CE, et al. Influence of antimicrobial chemotherapy on spirometric parameters and pro-inflammatory indices in severe pulmonary tuberculosis. Eur Respir J 1998; 12: 351–356. 
  6. Ross J, Ehrlich RI, Hnizdo E, et al. Excess lung function decline in gold miners following pulmonary tuberculosis. Thorax 2010; 65: 1010–1015. 
  7. Pasipanodya JG, Miller TL, Vecino M, et al. Pulmonary impairment after tuberculosis. Chest 2007; 131: 1817–1824. 
  8. Pasipanodya JG, McNabb SJ, Hilsenrath P, et al. Pulmonary impairment after tuberculosis and its contribution to TB burden. BMC Public Health 2010; 10: 259. 
  9. Maguire GP, Anstey NM, Ardian M, et al. Pulmonary tuberculosis, impaired lung function, disability and quality of life in a high-burden setting. Int J Tuberc Lung Dis 2009; 13: 1500–1506. 
  10. Laney A.S, Weissman D.N. Respiratory diseases caused by coal mine dust.
  11. J Occup Environ Med. 2014; 56: S18-S22, View in Article Scopus (64) PubMed Cross ref Google Scholar
  12. Tse L.A. Dai J. Chen M. et al. Prediction models and risk assessment for silicosis using a retrospective cohort study among workers exposed to silica in China.Sci Rep. 2015; 5: 11059View in Article Scopus (25) PubMed Cross ref Google Scholar
  13. Akgun M. Araz O. Ucar E.Y. et al. Silicosis appears inevitable among former denim sandblasters: a 4-year follow-up study. Chest. 2015; 148: 647-654 View in Article Scopus (37) PubMed Cross ref Google ScholarNational Assembly of Zambia
  14. The occupational health and safety bill, 2010 National Assembly of Zambia, Lusaka (2010) [Online] Available from:http://www.parliament.gov.zm/sites/default/files/documents/bills/The%20Occupation al%20Health%20and%20Safety%20Bill%202010_0.pdf[Accessed on 24th February, 2016] Google Scholar View in article Ministry of Health
  15. Annual health statistical bulletin 2011 Ministry of Health, Lusaka (2013) [Online] Available from:http://www.moh.gov.zm/docs/reports/2011_Annual_Health_Bulletin_%20FINAL%2 0VERSION.pdf[Accessed on 24th February, 2016] Google Scholar View in article
  16. Pascalina Chanda-Kapata, Doris Osei-Afriyie, Connrad Mwansa and Nathan Kapata. (2016) Tuberculosis in the mines of Zambia: A case for intervention. Zambia
  17. Sustainable development goals [website]. New York: United Nations; (https://sustainabledevelopment.un.org/topics/sustainabledevelopmentgoals, accessed 20 July 2020).
  18. World Health Organization. Resolution WHA67.1. Global strategy and targets for tuberculosis prevention, care and control after 2015. Geneva: World Health Organization; 2014 (http://apps.who.int/gb/ebwha/pdf_files/WHA67/A67_R1-en.pdf, accessed 20 July 2020)
  19. United Nations General Assembly. Resolution 73/3: Political declaration of the high- level meeting of the General Assembly on the fight against tuberculosis. United Nations; 2018 (https://www.un.org/en/ga/search/view_doc.asp?symbol=A/RES/73/3, accessed 20 July 2020).
  20. The Global Plan to End TB, 2018–2022. Geneva: Stop TB Partnership; 2019 (http://stoptb.org/global/plan/plan1822.asp, accessed 20 July 2020).
  21. Floyd K, Glaziou P, Houben R, Sumner T, White RG, Raviglione M. Global tuberculosis targets and milestones set for 2016-2035: definition and rationale. Int J Tuberc Lung Dis. 2018;22(7):723–30 (https://www.ncbi.nlm.nih.gov/pubmed/29914597, accessed 20 July 2020).
  22. Report of the Secretary-General. Progress towards achieving global tuberculosis targets and implementation of the UN political declaration on tuberculosis. Seventy- fifth session. Agenda Item 132. Global health and foreign policy. United Nations; 2020 (https://undocs.org/en/A/75/236, accessed 24 September 2020).
  23. World Health Organization. Global Health Estimates 2016: Deaths by Cause, Age, Sex, by Country and by Region, 2000-2016. Geneva, World Health Organization 2018. (https://www.who.int/news-room/fact-sheets/detail/the-top-10-causes-of-death, accessed 20 July 2020).
  24. F. M. McPhendran and E. L. Opie, “ e spread of Tuberculosis in families,” American Journal of Epidemiology,vol.22,no.3,pp. 565–643, 1935
  25. 25.    J. B. Shaw and N. Wynn-Williams, “Infectivity of pulmonary tuberculosis in relation to sputum status,” American Review of Tuberculosis,vol.69,no.5,pp.724–732,1954.
  26. 26.    D. Maher, “the natural history of Mycobacterium tuberculosis infection in adults,” in Tuberculosis: A Comprehensive Clinical Reference, H. S. Schaaf and A. Zumla, Eds., pp. 129–132, Elsevier
  27.  
  28. Health Sciences, 2009
  29. 27.    N. Ait-Khaled and D. Enarson, Tuberculosis: A manual for medical Students, World Health Organization, 2003.
  30. 28.    R. Joshi, A. L. Reingold, D. Menzies, and M. Pai, “Tuberculosis among health-care workers in low- and middle-income countries: a systematic review,” PLoS Medicine,vol.3,no.12,article
  31. e494, 2006
  32. 29.    B. Alisjahbana, R. Van Crevel, E. Sahiratmadja, M. den Heijer,
  33. A.    Maya,E.Istrianaetal.,“Diabetesmellitusisstrongly associated with tuberculosis in Indonesia,” the International
  34. Journal of Tuberculosis and Lung Disease,vol.10,no.6,pp.696– 700, 2006.
  35. 30.    S.J.Kim,Y.P.Hong,W.J.Lew,S.C.Yang,andE.G.Lee,“Incidence of pulmonary tuberculosis among diabetics,” Tubercle and Lung Disease,vol.76,no.6,pp.529– 533,1995.
  36. 31.    World Health Organization, “Equity, Social Determinants and Public Health Programmes,” Geneva: World Health Organization, http://books.google.co.in/books?id=7JxutqCmctUC, 2010
  37. 32.    W. Rathmann, G. Giani, S. H. Wild et al., “Global prevalence of diabetes: estimates for the year 2000 and projections for 2030,” Diabetes Care,vol.27,no.10,pp.2568–2569, 2004.
  38. 33.    K. Lonnroth, B. G. Williams, S. Stadlin, E. Jaramillo, and C.
  39. Dye, “Alcohol use as a risk factor for tuberculosis-a systematic review,” BMC Public Health,vol.8,article289,2008.
  40. 34.    World Health Organization [homepage on the Internet]. Geneva: World Health Organization; [cited 2016 Dec 1]. Global Health Risks: Mortality and burden of disease attributable to selected major risks. [Adobe Acrobat document, 70p.]. Available from: http://www.who.int/healthinfo/global_burden_disease/GlobalHealthRisks_report_full. pdf
  41. 35.    Rehm J, Samokhvalov AV, Neuman MG, Room R, Parry C, Lönnroth K, Patra J, Poznyak V, Popova S. The association between alcohol use, alcohol use disorders and tuberculosis (TB). A systematic review. BMC Public Health. 2009;9:450. https://doi.org/10.1186/1471-2458-9-450
  42. 36.    J. P. Cegielski and D. N. McMurray, “ e relationship between malnutrition and tuberculosis: evidence from studies in humans and experimental animals,” International Journal of Tuberculosis and Lung Disease,vol.8,no.3,pp.286–298,2004
  43. 37.    K. Lonnroth, B. G. Williams, P. Cegielski, and C. Dye, “A consistent log-linear relationship between tuberculosis incidence and body mass index,” International Journal of Epidemiology,vol.39, no. 1, Article ID dyp308, pp. 149–155, 2010.
  44. 38.    R. K. Chandra, “Nutrition and the immune system: an introduction,” The American Journal of Clinical Nutrition, vol.66,no.2, pp. 460S–463S, 1997.
  45. 39.    R. K. Chandra and S. Kumari, “Nutrition and immunity: an overview,” Journal of Nutrition,vol.124,supplement8,pp. 1433S–1435S, 1994
  46. 40.    K. Abba, T. D. Sudarsanam, L. Grobler, and J. Volmink, “Nutritional supplements for people being treated for active tuberculosis,” Cochrane Database of Systematic Reviews,no.4,Article ID CD006086, 2008.
  47. 41.    G.W.ComstockandC.E.Palmer,“Long-term results of BCG vaccination in the southern United States,” American Review of Respiratory Disease,vol.93,no.2,pp.171–183, 2008
  48.  
  49. 42.    K. R. Smith, “Indoor air pollution in developing countries: recommendations for research,” Indoor Air,vol.12,no.3,pp. 198–207, 2002.
  50. 43.    C. Kolappan and R. Subramani, “Association between biomass fuel and pulmonary tuberculosis: a nested case-control study,”thorax,vol.64,no.8,pp.705-708, 2009.
  51. 44.    A.K.Pokhrel,M.N.Bates,S.C.Verma,H.S.Joshi,C.T. Sreeramareddy, and K. R. Smith, “Tuberculosis and indoor biomass and kerosene use in Nepal: a case-control study,” Environmental Health Perspectives, vol.118,no.4, pp.558–564, 2010.
  52. 45.    Marques AC, Cruz MS. O adolescente e o uso de drogas. Rev Bras Psiquiatr. 2000;22(2):32-6. https://doi.org/10.1590/S1516-44462000000600009
  53. 46.    Deiss RG, Rodwell TC, Garfein RS. Tuberculosis and illicit drug use: review and update. Clin Infect Dis. 2009;48(1):72-82. https://doi.org/10.1086/594126
  54. 47.    van Zyl Smit RN, Pai M, Yew WW, Leung CC, Zumla A, Bateman ED, et al. Global lung health: the colliding epidemics of tuberculosis, tobacco smoking, HIV and COPD. Eur Respir J. 2010;35(1):27-33. https://doi.org/10.1183/09031936.00072909
  55. 48.    Bates MN, Khalakdina A, Pai M, Chang L, Lessa F, Smith KR. The risk of tuberculosis from exposure to tobacco smoke: a systematic review and meta-analysis. Arch Intern Med. 2007;167(4):335-42. https://doi.org/10.1001/archinte.167.4.335
  56. 49.    Lin HH, Ezzati M, Murray M. Tobacco smoke, indoor air pollution and tuberculosis: a systematic review and meta-analysis. PLoS Med. 2007;4(1):e20. https://doi.org/10.1371/journal.pmed.0040020
  57. 50.    Grant AD, Djomand G, De Cock KM. Natural history and spectrum of disease in adults with HIV/AIDS in Africa. AIDS1997; 11 (suppl B):S43–54.
  58. 51.    Munyati SS, Dhoba T, Makanza ED, et al. Chronic cough in primary health care attendees, Harare, Zimbabwe: diagnosis andimpact of human immunodeficiency virus. Clin Infect Dis2005;40:1818–27.
  59. 52.    Ansari NA, Kombe AH, Kenyon TA, et al. Pathology and causes ofdeath in a group of 128 predominantly HIV-positive patients inBotswana, 1997–1998. Int J Tuberc Lung Dis2002; 6:55–63.
  60. 53.    Lucas SB, Hounnou A, Peacock C, et al. The mortality and pathologyof HIV infection in a west African city. AIDS1993; 7:1569–79.
  61. 54.    Nelson AM, Perriens JH, Kapita B, et al. A clinical and pathologicalcomparison of the WHO and CDC case definitions for AIDS inKinshasa, Zaire: is passive surveillance valid? AIDS1993; 7:1241–45.
  62. 55.    Rana FS, Hawken MP, Mwachari C, et al. Autopsy study of HIV-1-positive and HIV- 1-negative adult medical patients in Nairobi,Kenya. J Acquir Immune Defic Syndr2000; 24:23–29.
  63. 56.    Van Cleeff MR, Kivihya-Ndugga L, Githui W, Nganga L, Odhiambo J, Klatser PR. A comprehensive study of the efficiency ofthe routine pulmonary tuberculosis diagnostic process in Nairobi.Int J Tuberc Lung Dis2003; 7:186–89.
  64. 57.    Harries AD, Kamenya A, Subramanyam VR, et al. Screeningpulmonary tuberculosis suspects in Malawi: testing differentstrategies. Trans R Soc Trop Med Hyg1997; 91:416–19.
  65. 58.    Scott JAG, Hall AJ, Muyodi C, et al. Aetiology, outcome, and risk factors for mortality among adults with acute pneumonia in Kenya.Lancet2000; 355:1225–30
  66. 59.        Banda HT, Harries AD, Welby S, et al. Prevalence of tuberculosis in TB suspects with short duration of cough. Trans R Soc Trop Med Hyg1998; 92:161–63
  67. 60.    Archibald LK, den Dulk MO, Pallangyo KJ, Reller LB. FatalMycobacterium tuberculosisbloodstream infections in febrilehospitalized adults in Dar es Salaam, Tanzania. Clin Infect Dis1998;26:290–96
  68.  
  69. 61.    Mwachari C, Batchelor BI, Paul J, Waiyaki PG, Gilks CF. Chronicdiarrhoea among HIV-infected adult patients in Nairobi, Kenya. J Infect 1998; 37:48–53.
  70. 62.    Cauthen G. M., Pio A., ten Dam H. G. Annual Risk of Tuberculous Infection. 1988. Bulletin of the World Health Organization. 2002;80:503–11. [PMC free article] [PubMed] [Reference list]
  71. 63.    Ministry of Health, National tuberculosis prevalence survey 2013–2014: technical report, Ministry of Health, Lusaka (2015), [Online] Available from: http://www.moh.gov.zm/docs/reports/zntbs13-14_final.pdf, [Accessed on 24th February, 2016], Google Scholar, View in article
  72. 64.    N. Kapata, P. Chanda-Kapata, M.P. Grobusch, J. O'Grady, S. Schwank, M. Bates, et al. Scale-up of TB and HIV programme collaborative activities in Zambia – a 10- year review Trop Med Int Health, 17 (6) (2012), pp. 760-766 Cross Ref View Record in Scopus Google Scholar View in article
  73. 65.    Central Statistical Office Zambia demographic health survey 2013–2014 Central Statistical Office, Lusaka (2015) [Online] Available from: http://pdf.usaid.gov/pdf_docs/PBAAC524.pdf [Accessed on 24th February, 2016]Google Scholar View in article
  74. 66.    N. Kapata, P. Chanda-Kapata, J. O'Grady, S. Schwank, M. Bates, V. Mukonka, et al.
  75. Trends of Zambia's tuberculosis burden over the past two decades Trop Med Int Health, 16 (11) (2011), pp. 1404-1409
  76. Cross Ref View Record in Scopus Google Scholar View in article
  77. 67.    World Health Organization Global tuberculosis report 2015 World Health Organization, Geneva (2015) [Online] Available from:http://www.who.int/tb/publications/global_report/en/ [Accessed on 24th February, 2016] Google Scholar View in article
  78. 68.    A. Zumla, E. Petersen, T. Nyirenda, J. Chakaya
  79. Tackling the tuberculosis epidemic in sub-Saharan Africa–unique opportunities arising from the second European Developing Countries Clinical Trials Partnership (EDCTP) programme 2015–2024 Int J Infect Dis, 32 (2015), pp. 46-49 Article
  80. Download PDF View Record in Scopus Google Scholar View in article
  81. 69.    Bambas-Nolehn L, Birn AE, Cairncross E, Kisting S, Liefferink M, Mukhopadhyay B, et al. Case study on extractive industries prepared for the lancet commission on global governance. [Online] Available from: https://www.med.uio.no/helsam/english/research/global-governance- health/background-papers/extrac-indus.pdf [Accessed on 24th February, 2016]. Google Scholar View in article
  82. 70.    I.A. Saidu, Z. Nasir, B.W. Goni  
  83. Social determinants of tuberculosis in sub-Saharan Africa: a systematic review Glob J Med Public Health, 3 (4) (2014), pp. 1-14 View Record in ScopusGoogle Scholar View inarticle
  84. 71.    D. Stuckler, S. Basu, M. McKee, M. Lurie Mining and risk of tuberculosis in sub-Saharan Africa
  85. Am J Public Health, 101 (3) (2010), pp. 524-530 View Record in ScopusGoogle Scholar View inarticle
  86. 72.    W. Utembe, E.M. Faustman, P. Matatiele, M. Gulumian Hazards identified and the need for health risk assessment in the south African mining industry Hum Exp Toxicol, 34 (12) (2015), pp. 1212-1221
  87. Cross Ref View Record in Scopus Google Scholar View in article
  88. 73.    H.H. Park, B.V. Girdler-Brown, G.J. Churchyard, N.W. White, R.I. Ehrlich Incidence of tuberculosis and HIV and progression of silicosis and lung function impairment among former Basotho gold miners
  89. Am J Ind Med, 52 (12) (2009), pp. 901-908
  90. Cross Ref View Record in Scopus Google Scholar View in article
  91. 74.    Handicap International. Knowledge, attitudes and practices in risk education: carrying out KAP surveys. 2009. Available online at: http://www.handicap- international.org.uk/Resources/Handicap%20International/PDF%20Documents/HI%2 0Associations/KAPRiskEducation_2009.pdf.
  92. 75.    World Health Organization. A guide to developing knowledge, attitude, and practice surveys. Geneva, Switzerland: World Health Organization, 2008. Available online at: http://www.stoptb.org/assets/documents/resources/publications/acsm/ACSM_KAP%2 0GUIDE.pdf.
  93. 76.    Rees, D., et al. Oscillating migration and the epidemics of silicosis, tuberculosis, andHIV infection in South African gold miners.Am. J. Ind. Med.53(4):398–404, 2010.doi: 10.1002/ajim.20716
  94. 77.    Williams, B. G., et al. Occupational health, occupational illness: Tuberculosis,silicosis and HIV on the South African mines. InOccupational Lung Disease: AnInternational Perspective, ed. D. Banks and J. Parker. Chapman and Hall, London,1998.
  95. 78.    National Institute of Occupational Health: Mine Health and Safety Council.WhatDoes Silicosis Reduction Mean to Mineworkers? Johannesburg, 2010.
  96. 79.    Hanifa, Y., et al. Prevalence of latent tuberculosis infection among gold miners in South Africa.Int. J. Tuberc. Lung Dis.13 (1):39–46, 2009.
  97. 80.    Charalambous, S., et al. Contribution of reinfection to recurrent tuberculosis in SouthAfrican gold miners.Int. J. Tuberc. Lung Dis.12(8):942–948, 2008.
  98. 81.    World Health Organization.Global Tuberculosis Control. Geneva, 2011.
  99. 82.    Basu, S., et al. The production of consumption: Addressing the impact of mineralmining on tuberculosis in southern Africa.Global. Health5:11, 2009. doi: 10.1186/1744-8603-5-11.
  100. 83.    Ross MH, Murray J. Occupational respiratory disease in mining. Occup Med Oxf Engl. 2004;54(5):304–10.
  101. 84.    Stuckler D, Steele S, Lurie M, Basu S. “Dying for gold”: the effects of mineral mining on HIV, tuberculosis, silicosis and occupational diseases in southern Africa. Int J Health Serv Plan Adm Eval. 2013;43(4):639–49.
  102.  
  103. 85.    Mohapatra H, Goswami S, Dey D. Coalmine dust concentration and rate of tuberculosis infection around Ib Valley Coalfield, Orissa, India. J Environ Biol. 2010 Nov;31(6):953–6
  104. 86.    Murray J, Davies T, Rees D. Occupational lung disease in the South African mining industry: research and policy implementation. J Public Health Policy. 2011;32 Suppl 1:S65–79.
  105. 87.    Han L, Han R, Ji X, Wang T, Yang J, Yuan J, et al. Prevalence characteristics of coal workers’ pneumoconiosis (CWP) in a state-owned mine in Eastern China. Int J Environ Res Public Health. 2015;12(7):7856–67.
  106. 88.    Dweik R, Mazzone P. Occupational lung disease. Lyndhurst, OH: The Cleveland Clinic Foundation; 2010 (http://www.clevelandclinicmeded.com/medicalpubs/ diseasemanagement/pulmonary/occupational-lungdisease/, accessed 26 October 2015
  107. 89.    Innes A. Zhao Tong, Yunnan: fighting TB in its mountain stronghold. Washington, DC: U.S. Agency for International Development (https://www.cap-tb.org/ blog/zhao- tong-yunnan-fighting-tb-its-mountainstronghold, accessed 26 October 2015).
  108. 90.    Onozuka D, Hagihara A. Geographic prediction of tuberculosis clusters in Fukuoka, Japan, using the spacetime scan statistic. BMC Infect Dis. 2007;7:26.
  109. 91.    Stuckler D, Basu S, McKee M. Governance of mining, HIV and tuberculosis in southern Africa. Glob Health Gov. 2010;4(1) (http://researchonline.lshtm.ac.uk/1376/, accessed 30 October 2015).
  110. 92.    E.M. Mulenga, H.B. Miller, T. Sinkala, T.A. Hysong, J.L. Burgess Silicosis and tuberculosis in Zambian miners Int J Occup Environ Health, 11 (3) (2005), pp. 259-262 View Record in ScopusGoogle Scholar
  111. 93.    Comprehensive HIV AIDS Management Programme Cost benefit analysis of HIV workplace programmes in Zambia Comprehensive HIV AIDS Management Programme, Lusaka (2007) [Online] Available from: http://www.iom.int/jahia/webdav/shared/shared/mainsite/media/docs/reports/cos t_benefit_analysis.pdf[Accessed on 24th February, 2016]Google Scholar
  112. 94.    Human Rights Watch “You'll be fired if you refuse”. Labor abuses in Zambia's Chinese state- owned copper mines Human Rights Watch, New York (2011) [Online] Available from:
  113. https://www.hrw.org/sites/default/files/reports/zambia1111ForWebUpload.pdf [Accessed on 24th February, 2016]
  114. Google Scholar
  115. 95.    A. Farazi, M. Jabbariasl Silico-tuberculosis and associated risk factors in central province of Iran
  116. Pan Afr Med J, 20 (2015), p. 333 View Record in ScopusGoogle Scholar
  117. 96.    World Health Organisation. Tuberculosis notification rate, 2019. https://rho.emro.who.int
  118.  
  119. 97.    Wits Health Consortium (WHC). (2017) Knowledge, Attitudes and Practises (KAP) on TB, HIV and Silicosis Among Key Populations Aged 15 and 59 years in Southern Africa. Zimbabwe: Pvt ltd.
  120. 98.    Abiy Tadesse Angelo, Teketel Ermias Geltore and Tagay Asega, (2019). Knowledge, Attitude, and Practices Towards Tuberculosis Among Clients Visiting Tepi General Hospital Outpatient Departments. Ethiopia
  121. 99.    Kazaura M, Kamazima SR (2021) Knowledge, attitudes and practices on tuberculosis infection prevention and associated factors among rural and urban adults in northeast Tanzania: A cross-sectional study. PLOS Glob Public Health 1(12): e0000104. https://doi.org/10.1371/journal. pgph.0000104
  122. 100.    Laura Jean Podewils, Elizabeth F. Long, Tyler J. Fuller. Et al, (2022). Zambia Assessment of Tuberculosis (TB) and HIV in the Mines (ZATHIM): implications
  123. for programs and policies. Zambia, https://doi.org/10.1186/s12889-022-13053-8.