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PLoS One. 2017; 12(9): e0183749.
Published online 2017 September 8. doi:  10.1371/journal.pone.0183749
PMCID: PMC5590832

Stakeholder perspectives for optimization of tuberculosis contact investigation in a high-burden setting

Diana Marangu, Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Software, Visualization, Writing – original draft,1,2,* Hannah Mwaniki, Data curation, Formal analysis, Software, Validation, Writing – review & editing,3 Salome Nduku, Data curation, Formal analysis, Validation, Writing – review & editing,4 Elizabeth Maleche-Obimbo, Conceptualization, Formal analysis, Methodology, Supervision, Visualization, Writing – review & editing,1 Walter Jaoko, Conceptualization, Formal analysis, Methodology, Supervision, Visualization, Writing – review & editing,5 Joseph Babigumira, Conceptualization, Formal analysis, Methodology, Supervision, Visualization, Writing – review & editing,6 Grace John-Stewart, Conceptualization, Formal analysis, Methodology, Supervision, Visualization, Writing – review & editing,6,7,8,9 and Deepa Rao, Conceptualization, Formal analysis, Methodology, Supervision, Visualization, Writing – review & editing6,10
Madhukar Pai, Editor

Abstract

Introduction

Optimal tuberculosis contact investigation impacts TB prevention, timely case finding and linkage to care, however data on routine implementation in high burden contexts is limited.

Materials and methods

In a multi-method qualitative study based on individual interviews with TB patients, facility observations and focus group discussions with health workers (HWs) in 13 public health facilities, and key informant interviews with governmental and non-governmental experts, we describe TB contact investigation in the context of an urban setting in Kenya and identify opportunities for optimization.

Results

Invitation of TB patients to bring close contacts by HWs was key for all patient decisions that led to contact screening in addition to patients’ understanding of TB transmission and desire to avoid contacts suffering from TB. Sub-optimal HW enquiry of TB patients and contacts presenting at the facility were missed opportunities which stemmed from lack of standardized operational procedures, documentation tools and HW training. Stakeholders proposed provision of fast tracked and holistic health packages for contacts seeking TB screening, and sustainable government led funding for the requisite infrastructure and workforce.

Conclusion

TB contact invitation by HWs leading to contact screening occurs in this context. Stakeholder perspectives inform the design of an operational framework for optimized delivery.

Introduction

In 2015, it was estimated that 41% of the 10.4 million people with active tuberculosis (TB) worldwide were undiagnosed or unreported [1]. In a meta-analysis of 71 studies including 878,724 participants in low and middle income countries (LMICs), pooled prevalence of TB among persons who were exposed to TB was 3.1%, and in 76 studies pooled prevalence of latent TB infection was 51.5% among 60,557 contacts screened [2]. The World Health Organization (WHO) considers contact investigation (CI) an efficient approach to intensified TB case finding and it is one of 10 indicators of the End TB Strategy, with a recommended target level of ≥ 90% by 2025 [1, 3]. The TB-CI strategy identifies asymptomatic individuals, including children and HIV infected individuals, who are at high risk for TB disease [49]. TB-CI is a gateway to isoniazid preventive therapy (IPT) delivery and part of TB care. Although CI has been shown to be feasible in some LMICs [10], data on routine TB-CI implementation in high TB burden contexts is scarce.

The WHO advises that TB-CI may be of value in high HIV/multidrug resistant (MDR) TB contexts as these are known to reduce TB treatment success rates [7, 11]. Gaps in specific policy, guidelines, tools and financial resources for CI scale-up have been recognized in these settings. However, the implementation of routine TB-CI has not been formally assessed [12]. We sought to examine TB-CI by characterizing experiences of index TB patients seeking care in Nairobi, a densely populated city in a high burden HIV, TB and MDR-TB LMIC. In addition, we sought to identify and describe health system facilitators, barriers and opportunities for optimization from the perspectives of health workers (HWs) and experts involved in TB-CI related care provision.

Materials and methods

Following ethical approval from the University of Nairobi-Kenyatta National Hospital Ethics and Research Committee and the University of Washington Institutional Review Board, we conducted this multi-method qualitative study between April 2015 and July 2016.

Research team and reflexivity

The team included senior researchers with extensive experience in the fields of qualitative research, TB-HIV and health economics. The first author, a Kenyan pediatrician with formal training and experience in qualitative research made facility observations and conducted individual patient interviews, key informant interviews (KIIs) and focus group discussions (FGDs) with study participants without establishing a relationship prior to the start of the study. The second author, a Kenyan population studies researcher and anthropologist with extensive qualitative research experience transcribed all the interviews. These two multi-lingual researchers independently coded the transcripts and resolved differences in the analysis by consensus. The third author, a Swahili/English Translator and Communicator with over 10 years of experience in translation and localization, independently reviewed the TB patient interviews to ensure recommendations proposed accurately reflected patient needs.

Participant selection

Participants comprised of three groups of stakeholders: TB patients, HWs, and experts involved in various areas of TB care in Kenya. As described in the Kenya Health Policy 2014–2030, the health delivery system is progressively transforming into four tiers of care: community, primary care, secondary referral care, and tertiary referral care. Level II (dispensaries) and level III (health centres) facilities are to provide primary care, whereas level IV (primary care hospitals) and level V (secondary care hospitals) facilities will provide secondary referral care [13]. We selected study participants from 13 TB clinics in public health facilities in Nairobi, Kenya, stratified by the level of health care provided as shown in Fig 1. These included all tertiary and secondary public referral facilities in Nairobi County offering TB services. We also randomly sampled one facility from each of the nine sub-counties among 27 public primary health facilities listed in the 2014 master-list of health facilities [14].

Fig 1
Schema of sampling frame of stakeholders involved in TB care in Nairobi County, Kenya.

TB patients

Index TB patients were selected to gain individual perspectives in decision making for TB screening, and were eligible if they had clinician-diagnosed pulmonary TB, were aged ≥18 years and attending the selected TB clinics. On two separate visits at each selected TB clinic, the researcher consecutively selected the first male and female patients from the TB patient register at the time of the visit. Where gender balance was not possible at the visit, a second participant of the same gender was conveniently selected. Therefore four patients from each of the 13 health facilities were selected with the goal of having a balanced sex distribution where possible.

Health workers

We selected HW provider teams responsible for TB-CI at each of these selected clinics to gain their ‘on the ground’ perspective. These teams comprised of various cadres involved in TB care including nurses, clinical officers, community health workers (CHWs), HIV counselors, social workers and laboratory technicians. The teams’ working relationship was leveraged to provide a safe environment to generate and gain valuable insights during the focus group discussions.

Key informants

Key informants who were experts involved in diverse aspects of TB-CI including policy makers, program implementers, academia, and industry, were purposefully selected to gain an in depth understanding of the health system in relation to TB-CI.

The lead researcher invited these stakeholders to participate in the study, sought informed written consent from each participant and conducted face-to-face interviews and FGDs during hours of facility or institution operation.

Data collection process

Prior to study commencement, the research team created a hypothetical TB-CI decision model for index TB patients with plausible decision arms based on existing literature and prior clinical experience. (Fig 2) The lead researcher used this hypothetical model to guide open ended interviews with individual TB patients. After obtaining informed consent, the researcher established rapport, enquired about pertinent sociodemographic characteristics such as a) age, b) education level, c) occupation, d) duration since TB diagnosis, e) living dynamics with regard to household and close contacts, f) where TB patients spent most of their time including travel, g) processes that took place at the health facility, h) the health education given by the HW and i) close contacts and the general TB care provided. Thereafter we enquired about facilitators, barriers and opportunities for TB contact screening optimization at each decision node. Our facility observation flow mapping guide and focus group discussion/interview guide are provided. (S1 and S2 Tables) To guide FGDs and documentation of facility observations including mapping flow of TB-CI related activities, we used the WHO’s six building blocks framework. These building blocks include: 1) health service delivery, 2) health workforce, 3) health information systems, 4) access to essential medical products, vaccines and technologies, 5) health systems financing and 6) leadership and governance. Since health systems are highly context-specific, this framework enables a health system to be analyzed in its totality, utilizing a unified approach that allows for identification of strengths and gaps [15]. In addition to the insights gained from HWs during the FGDs regarding general and TB-CI care at their facilities, we also provided scenarios to gauge the spectrum of TB-CI actions specific to contacts who were children or who were HIV-infected. During individual interviews, FGDs and KIIS, no one else was present during data collection besides the participants and lead researcher. The researcher audio recorded the interviews; took field notes and noted when data were saturated. Interviews were transcribed verbatim by the second author. We did not repeat interviews or return transcripts to participants for comments or correction. To maintain confidentiality, we did not audio record participant names during interviews. We stored data in password protected files with access restricted to researchers, and destroyed audio-recorded files six months after transcription as per our protocol.

Fig 2
Hypothetical decision model: Index TB patients’ decisions on contact investigation.

Analyses

We were able to validate our data by cross verifying multiple sources (health facilities, TB patients, HWs and key informants) and utilizing different qualitative methodologies (observations, interviews and focus group discussions). Data analysis was at three levels: patient, HW and health system. At the patient level analysis, we assessed the TB-CI decision model based on two decision levels: Was the TB patient invited by a HW to bring his/her close contacts for TB screening? Were any of the close contacts screened for TB? At each decision node we identified facilitators, barriers and opportunities for TB-CI optimization and analyzed themes. We also analyzed data from facility observations, HW FGDs and stakeholder KIIs, and synthesized themes using WHO’s six health system building blocks [15]. To ensure data validity, the lead researcher and second author independently analyzed the data and settled differences via consensus. We manually coded the transcripts and also used Atlas.ti GmbH, Berlin version 7.5.10 (Student License) to manage the data [16]. Patient interviews were independently reviewed by the third author to ensure proposed recommendations accurately reflected patient needs.

Results

Participant characteristics

We conducted this qualitative study including 52 adult TB patients. As shown in Table 1, 27 (52%) were male, the median age was 33 years (IQR 26–40, range 21–50) and 36 (69%) were from primary health facilities. Thirty seven patients (71%) had attained eight complete years of primary school education and thirty five patients (67%) were employed/self-employed. Patients had diverse occupations including managers, administrators, marketers, shop assistants, hair stylists, tailors, mechanics, public vehicle drivers and conductors, barmaids, cleaners, casual laborers and businessmen/women selling cooked food, charcoal, khat and art among specified items. Three patients (6%) were college/university students. The remainder (27%) were unemployed comprising housewives, those with no jobs/looking for jobs and one refugee. Approximately two thirds of patients lived with either members of their nuclear or extended families. In 13 FGDs we conducted among HWs in each selected facility, the median number of participants was 7 HWs (IQR 6–8). (Table 2) Key informants involved in TB-CI related activities comprised 5 policy makers/implementers in government, 4 policy makers/implementers in non-governmental organizations, 5 respiratory health experts in pediatric and adult medicine including academic faculty in public and private sectors, and 3 health information system consultants. (Fig 3)

Table 1
TB patient characteristics.
Table 2
Health worker focus group characteristics.
Fig 3
Key informant characteristics.

Index TB patients’ decision making on bringing contacts

From the individual patient interviews, most (37/52) patients seeking TB care at the facilities were invited by a HW to have their contacts screened and almost half (22/52) had at least one contact screened for TB. All TB patients whose contacts underwent screening were invited by a HW. Of 15 TB patients invited by a HW but did not have their contacts screened, 7 reported they would have their close contacts screened if they were symptomatic, 4 would bring at least one close contact on a specific date in the future, and the remainder reported: not feeling well /no finances to bring contacts/contacts busy. Approximately half of the TB patients who did not have their contacts screened but expressed willingness to come if invited. (Table 3)

Table 3
Patient identified facilitators and barriers to having contacts screened.

Facilitators

Invitation of TB patients by HWs to bring close contacts was key to successful TB-CI. Patients reported that good rapport with HWs via flexibility, consideration, and generally handling patients well were facilitators for TB-CI. Additional facilitators included CHW home-visits and HW provision of sputum containers for unavailable contacts to overcome barriers such as contacts being at work or in school, and talking to family members, particularly husbands who were reported to be difficult to convince to come to the facility for TB-CI. Patients’ desire to avoid contacts suffering from TB, their concern for each other’s health, as well as the positive health changes that were seen once on treatment also promoted TB-CI activities. Screening of close contacts was also facilitated by the identification of TB in children (reverse CI). Furthermore, patients reported that HWs utilized TB-CI for provision of IPT for eligible contacts including children under the age of five years. Experts acknowledged strengths in the health system which included a resilient health workforce, supportive structures for service delivery, supervision in the TB, HIV and Community Health programs and strong multi-sectoral government leadership. (Tables (Tables33 and and4;4; Fig 4)

Table 4
Facility observations, health worker and key informant perspectives on implementation of TB contact investigation.
Fig 4
Operational framework for optimizing tuberculosis contact investigation.

Barriers

Lack of operating procedures, documentation and HW training specific to TB-CI were the main barriers to its optimal implementation. On asking HWs whether TB patients brought their contacts/had their close contacts screened for TB, the response was either “few” or “some” in all the 13 FGDs. Sub-optimal HW enquiry of contacts noted from individual patient interviews, particularly those who lived alone, had child contacts who were asymptomatic/not part of the nuclear family, or close contacts out of town, may have led to lack of HW invitation. The TB register present in all TB clinics had a column for TB patients identified due to contact investigation, however this was rarely checked. There was no standardized tool in the facility for ascertaining that HWs had invited TB patients to have their contacts screened and neither was there a tool that linked TB patients to their contacts. During this study period, there were active TB-CI activities conducted in selected facilities in Nairobi County in the context of programs funded by non-governmental organizations and 10 of the 13 facilities were participating. Despite contacts in the community being referred to the facility for screening, they did not receive any documentation that would identify them to the facility as being referred for contact investigation, hence it was difficult to measure the efficacy of this active TB-CI activity. Similar to the passive TB-CI facility approach, a mechanism to link contacts to a particular TB patient was lacking, making it difficult to establish if all close contacts had been screened and estimate effectiveness of this strategy.

TB-related stigma among TB patients emerged as a major barrier to TB-CI and linkage to care in patient and expert interviews as well as all the HW FGDs (13/13). Patients generally had poor knowledge on the cause of TB and how it was transmitted. The presumption that all TB patients had HIV and misconceptions regarding TB transmission were common, including through sex, sharing utensils and genetics. CHWs cited experiencing near-violent encounters when visiting patients’ homes due to patients’ fear of their TB status being known by others, and others found that patients provide wrong home addresses and/or phone numbers to avoid CHWs visiting their homes–possibly fearing inadvertent disclosure. HWs in some facilities reported experiencing enacted stigma from colleagues who refused to work in the TB clinic areas for fear of infection. Few patients also reported HW enacted TB stigma while seeking TB care. Conversely, HWs reported they put themselves at risk for TB transmission by not putting on masks as they did not want to be seen to perpetuating stigma. (Tables (Tables334; Fig 4)

Opportunities for optimization

Key informants recognized the national TB program’s electronic surveillance and management system, TIBU, and proposed further innovation of the health management information system to support TB-CI that is user-friendly, efficient and interoperable. Experts explained that a national unique patient identifier was essential to avoid duplication of records and allow for linkage of data, and acknowledged that the government was taking the lead in this process. Additionally, stakeholders proposed fast-tracked care for contacts undergoing screening instituted in health facilities to avoid TB infection. Sustainable government-led funding for infrastructure, an adequate health workforce that is trained to deliver optimized TB-CI services, and social protection schemes to avert catastrophic costs were deemed imperative.

Considering program requirements and lessons learnt from stakeholder perspectives, specific areas of optimization that could be incorporated in facility based and/or community based TB CI strategies are outlined in Fig 4.

Discussion

Through the lens of TB patients attending public TB clinics, HWs, key informants and facility observations, we were able to understand how TB-CI is undertaken in the capital city of a high TB/MDR/HIV burden country. Although CI has traditionally not been part of TB control efforts in LMICs [2], most TB patients in this context brought or encouraged their contacts to undergo TB screening if they were invited by a HW in both passive/active approaches. Similar to a study in Vietnam, approximately one-third of TB patients did not know about the need of investigating contacts [17]. Most of the TB patients not invited by HWs expressed willingness to bring their contacts if they had been invited, underscoring the fundamental role HWs play and a potential area for TB-CI optimization.

Despite HW invitation being key for screening of TB contacts, clear operational guidelines and procedures for systematic enquiry by HWs, and documentation tools were lacking. The minimum requirements for TB-CI information to be reported have been documented [3]. Standardizing protocols for TB-CI and training HWs to adhere to protocols has been shown to be useful in performing effective CIs and in conducting studies on the effectiveness of TB-CI [18, 19]. Moreover, the systematic enquiry in TB-CI as has been described in the literature as both a science and an art, requiring effective interviewing skills [18]. Based on findings from patient interviews we identified the following as important considerations during enquiry: HW kindness and confidentiality [20]; HWs employing tactful probes to establish close contacts; patient sociodemographic characteristics including living dynamics; patient knowledge on TB etiology, transmission, treatment and prevention [17]; and preventing TB-related stigma [21, 22]. Additionally, providing fast-tracked healthcare deemed valuable to caregivers/relatives/friends accompanying patients [23] and child contacts [24, 25] is imperative. Regardless of the TB-CI approach, infection control and prevention measures are required to prevent acquiring new infections [26].

We believe that our study provides a current contextual analysis of TB-CI activities, highlighting opportunities for optimization and may inform the design of interventions addressing barriers to TB-CI in similar contexts. We propose to utilize the framework developed from these study findings on a platform that allows for linkage of index TB patients to their contacts using unique patient identifiers to assess its utility in TB-CI activities.

Conclusion

In conclusion, this study shows that TB contact invitation by HWs leading to contact screening does occur in the public health sector, however gaps exist. Key areas for optimization of TB-CI in this context include developing pragmatic TB-CI specific operational guidelines; a robust health information system that provides for documentation of TB-CI activities, linkage of index patients to their close contacts regardless of living dynamics, and referral and feedback loops; provision of holistic value added health packages for TB contacts undergoing TB screening, and sustainable government led community and health system interventions to promote TB-CI.

Supporting information

S1 Table

Observation flow mapping guide.

(DOCX)

S2 Table

Focus group discussion/interview guide.

(DOCX)

S3 Table

Consolidated criteria for reporting qualitative studies (COREQ).

(DOCX)

Acknowledgments

We wish to acknowledge all the TB patients, health workers and key informants who participated in this study, Professor James Pfeiffer and Leah Isquith facilitating the Advanced Anthropology Class at the University of Washington, University of Nairobi, International AIDS Research Training Program, and all other individuals and institutions that provided support to the ‘TB Kwisha’ Study.

Funding Statement

Diana Marangu is a recipient of the International AIDS Research Training Program (IARTP) MPH-PhD Implementation Science Scholarship funded by the Fogarty International Centre, National Institutes of Health (NIH) (1 D43 TW009580). Grace John-Stewart holds an NIH K24 Mentoring Award (K24 HD54314). Hannah Mwaniki and Salome Nduku received funding from the study budget as research assistants. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Data Availability

Data Availability

The data that support the findings of this study are included in this paper and its supplementary information files.

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