Systematic screening for

active tuberculosis:
an operational guide
Systematic screening for
active tuberculosis:
an operational guide

i
 WHO Library Cataloguing-in-Publication Data

Systematic screening for active tuberculosis: an operational guide

I.World Health Organization.

ISBN 978 92 4 154917 2

Subject headings are available from WHO institutional repository

© World Health Organization 2015

All rights reserved. Publications of the World Health Organization are available on
the WHO web site (www.who.int) or can be purchased from WHO Press, World
Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22
791 3264; fax: +41 22 791 4857;
e-mail: [email protected]).

Requests for permission to reproduce or translate WHO publications –whether for

sale or for non-commercial distribution– should be addressed to WHO Press
through the WHO website
(www.who.int/about/licensing/copyright_form/en/index.html).

The designations employed and the presentation of the material in this publication
do not imply the expression of any opinion whatsoever on the part of the World
Health Organization concerning the legal status of any country, territory, city or area
or of its authorities, or concerning the delimitation of its frontiers or boundaries.
Dotted lines on maps represent approximate border lines for which there may not
yet be full agreement.

The mention of specific companies or of certain manufacturers’ products does not

imply that they are endorsed or recommended by the World Health Organization in
preference to others of a similar nature that are not mentioned. Errors and
omissions excepted, the names of proprietary products are distinguished by initial
capital letters.

All reasonable precautions have been taken by the World Health Organization to
verify the information contained in this publication. However, the published
material is being distributed without warranty of any kind, either expressed or
implied. The responsibility for the interpretation and use of the material lies with
the reader. In no event shall the World Health Organization be liable for damages
arising from its use.

Printed in Switzerland
WHO/HTM/TB/2015.16

ii
Contents
Page
Acknowledgements 1

Definitions 2

Abbreviations 3

Executive summary 4

1. Introduction 5
1.1. Rationale for systematic screening for active TB 5
1.2. Pitfalls of screening 6
1.3. Objectives of the operational guide 6

2. The six steps of the planning and implementation cycle 10

2.1. Assessing the situation 10
2.2. Setting goals and specific objectives 17
2.3. Identification and prioritization of risk groups 18
2.4. Choosing screening and diagnostic algorithms 25
2.5. Planning, budgeting, and implementation 31
2.6. Monitoring, evaluation, and re-programming 35

3. Web-based tool to assist risk group prioritization and algorithm choices 40

3.1. Introduction to the tool 40
3.2. How to use the tool 41
3.3. Limitations of the tool 45

References 46

Annex: Ten potential screening and diagnostic algorithms 48

Additional information available online: http://who.int/tb/tbscreening/en/

x Tool to assist with prioritization of risk groups for screening and choice of algorithm
x Systematic screening for active tuberculosis: principles and recommendations
x Checklists for screening in specific risk groups
x Systematic reviews:
o The benefits to communities and individuals of screening for active tuberculosis
disease: a systematic review
o A systematic review of the sensitivity and specificity of symptom- and chest-
radiography screening for active pulmonary tuberculosis in HIV-negative
persons and persons with unknown HIV status
o A systematic review of number needed to screen to detect a case of active
tuberculosis in different risk groups
o Acceptability of TB screening among at-risk and vulnerable groups
o Acceptability of household and community-based TB screening in high burden
communities

iii
Acknowledgements
The development of this operational guide was led by Dr Knut Lönnroth (Global TB
Programme, WHO, Switzerland), who also wrote the first draft with assistance from Ms
Cecily Miller (American Thoracic Society, United States). Several drafts of the document
were reviewed and edited by a group of experts including: Dr Frank Bonsu (National TB
Programme, Ghana), Dr Erwin Cooreman (WHO Myanmar), Dr Jacob Creswell (Stop TB
Partnership, Switzerland), Dr Michel Gasana (Ministry of Health, Rwanda), Dr Pedro
Guillermo Suarez (Management Sciences for Health, United States), Dr Irwin Law (Global TB
Programme, WHO, Switzerland), Dr Ellen Mitchell (KNCV Tuberculosis Foundation, the
Netherlands), Dr Lindiwe Mvusi (National Department of Health, South Africa), Dr Nobuyuki
Nishikiori (WHO Regional Office for the Western Pacific), Dr Mao Tan Eang (National TB
Programme, Cambodia), Dr Anja Van’t Hoog (Amsterdam Institute for Global Health and
Development, the Netherlands), Ms Diana Weil (Global TB Programme, WHO, Switzerland),
Dr Rajendra Yadav (WHO Cambodia) and Ms Ruan Yunzhou (Centre for Disease Control,
China).

The online tool was developed by Dr Nobuyuki Nishikiori (WHO Regional Office for the
Western Pacific), Dr Knut Lönnroth and Ms Cecily Miller. Dr Anja van ‘t Hoog (Amsterdam
Institute of Global Health Development) assisted the development of the models for the
yield and cost of different screening and diagnostic algorithms.

The document was discussed in an expert consultation, as well as in a scientific symposium

at the 45th Union World Conference on Lung Health in Barcelona, Spain, in 2014.

This product was developed with partial support from the United States Agency for
International Development (USAID) under the TB CARE I Collaborative Agreement No. AID-
OAA-A-10-0020. The contents do not necessarily reflect the views of USAID or the United
States Government.

1
 Definitions
Active tuberculosis
Active tuberculosis (TB) refers to disease that occurs in someone infected with
Mycobacterium tuberculosis. It is characterized by signs or symptoms of active disease, or
both, and is distinct from latent TB infection, which occurs without signs or symptoms of
active disease.

Active tuberculosis case-finding

Active case-finding is synonymous with systematic screening for active TB, although it
normally implies screening that is implemented outside of health facilities.

Number needed to screen

The number needed to screen (or NNS) is the number of people that need to undergo
screening to diagnose one person with active TB.

Passive tuberculosis case-finding

This is a patient-initiated pathway to TB diagnosis involving: (1) a person with active TB
experiencing symptoms that he or she recognizes as serious; (2) the person having access to
and seeking care, and presenting spontaneously at an appropriate health facility; (3) a
health worker correctly assessing that the person fulfils the criteria for suspected TB; and (4)
the successful use of a diagnostic algorithm with sufficient sensitivity and specificity to
diagnose TB. Passive case-finding may involve an element of systematic screening if the
identification of people with suspected TB is done systematically for all people seeking care
in a health facility or clinic.

Risk groups
A risk group is any group of people in which the prevalence or incidence of TB is significantly
higher than in the general population.

Screening test, examination or procedure for active tuberculosis

A test, examination or other procedure for active tuberculosis distinguishing people with a
high likelihood of having active TB from people who are highly unlikely to have active TB. A
screening test is not intended to be diagnostic. People with positive results on a screening
test should undergo diagnostic evaluation.

Second screening
A second screening test, examination or other procedure applied to persons whose results
were positive during the initial screening.

Systematic screening for active TB

Systematic screening for active TB is the systematic identification of people with suspected
(presumptive) active TB, in a predetermined target group, using tests, examinations or other
procedures that can be applied rapidly. Among those screened positive, the diagnosis needs
to be established by one or several diagnostic tests and additional clinical assessments,
which together have high accuracy.

2
Abbreviations
CXR chest X-ray

HIV human immunodeficiency virus

NNS number needed to screen (to detect one true case of active tuberculosis)

PPV positive predictive value

TB tuberculosis

WHO World Health Organization

3
 Executive summary
More than one third of the 9 million people who fall ill with tuberculosis (TB) each year are
not diagnosed, not notified, or do not start treatment. Many of those who do start
treatment have a delayed start due to a range of challenges.1,2 Such obstacles to receive
care can result in poor health outcomes for the affected individuals, catastrophic costs for
their families and continued transmission of TB to others in their communities. In addition,
the individuals and communities at highest risk of falling ill with TB are often those with the
least access to health care and treatment for the disease, further compounding the negative
effects of the disease.

These barriers to care, coupled with the magnitude and persistence of the global TB burden,
argue for a redoubling of efforts to ensure early identification of and treatment for all
people with TB.3 To this end, the systematic screening of those at high risk for TB is a key
component of the World Health Organization’s (WHO) End TB strategy, 2016 to 2035. 4,5

Like all case-finding strategies, systematic screening for TB has three primary goals:
1. to ensure the early detection and initiation of appropriate treatment for those with
active TB;
2. to reduce the risk of poor treatment outcomes, health sequelae and the adverse social
and economic consequences of TB; and
3. to reduce transmission of TB, with the ultimate goal of reducing future incidence.

The WHO has published guidelines that set out the principles for screening for active TB and
provide recommendations on prioritizing of risk groups and choosing a screening approach.6
Screening should not be done on a mass, indiscriminate scale because this is expensive, of
relatively low benefit and can result in many false positive results. One of the key principles
set out in the guidelines is that screening for TB needs to be properly targeted to high-risk
groups and tailored to each specific situation, depending on the epidemiological, social and
health-systems contexts.

This document provides practical guidance on translating WHO’s principles and

recommendations into a national or local screening strategy by:
1. assessing the situation;
2. defining the objectives of screening;
3. prioritizing risk groups for screening;
4. choosing screening tools, algorithms and approaches for each risk group;
5. planning and budgeting for, and implementing the strategy;
6. monitoring and evaluating the strategy.

The guide includes a description of a web-based tool that can be used to help identify and
prioritize risk groups and chose appropriate screening and diagnostic algorithms. The tool is
designed to assist with the initial planning stages of creating a targeted screening strategy,
but several other factors than those covered by the tool need to be considered in the
planning process. This guide also includes additional online material, including other tools
and references to assist with planning and implementing screening programmes.

4
1. Introduction

1.1 Rationale for systematic screening for active TB

Concerted efforts during the past two decades – first under the DOTS strategy and later the
Stop TB Strategy – have made remarkable worldwide progress in controlling tuberculosis (TB)
and caring for patients with TB.3 However, millions of patients ill with TB are still not notified
to public health authorities, and the declines in TB deaths and incidence are still too slow.
These call for a redoubling of efforts for early identification and treatment of all cases of TB,
as envisioned in WHO’s End TB Strategy approved by the World Health Assembly in 2014. 4,5

Of the estimated 9 million persons who fall ill with TB each year, about 3 million are not
diagnosed and registered for quality-assured TB treatment.1 Additionally, many persons are
delayed in seeking care for their illness before they are eventually diagnosed and treated,2
and this can lead to worse health outcomes, higher costs for patients and their families, and
more transmission of the disease. Therefore, intensifying efforts to increase early case
detection is a key component of improving TB care and preventing the disease.

Detecting TB cases only from among persons presenting themselves to health facilities with
suggestive symptoms has until recently been the principal approach to case-finding.7,8 But
the remaining case-detection gap, particularly in certain vulnerable populations, along with
the persistence of delays in diagnosis and the accompanying continued transmission in the
community, highlight the need for a more active approach to detect TB early, hence the
need to consider systematic screening for active TB in selected risk groups.9-14

WHO’s End TB Strategy includes systematic screening for active TB in high-risk groups within
the first component of Pillar 1, which highlights the need for early diagnosis of TB. 4,5 The
World Health Organization (WHO) has published guidelines that set out the principles for
screening for TB and provide recommendations on prioritizing risk groups and choosing
screening approaches.6 The principles and recommendations are summarized in Box 1.

1.2 Pitfalls of screening

One of the key principles set out in the guidelines is that TB screening needs to be tailored
to each specific epidemiological, social and health-system situation, and planning for
screening must be based on an assessment of these contexts. Pursuing systematic screening
without planning properly to target the specific characteristics and needs of certain
populations, without assessing system capacity to deliver screening interventions, and
without first addressing the known constraints to case detection and treatment, may waste
resources without achieving clear individual and public-health benefits.

The cost of screening, especially as an outreach activity, can be high. The opportunity cost
must be considered and compared with other efforts to improve early TB detection, such as
improving access to diagnostic services. However, well-planned and well-targeted

5
 systematic screening has the potential to minimize avoidable delays in diagnosis and the
initiation of treatment. It thereby can contribute to improving the health of individuals as
well as reducing TB transmission.

Indiscriminate, mass screening is expensive and has uncertain benefits. Therefore, it should
be avoided. Screening low-risk groups can cause more harm than benefit – for example, by
detecting more false-positive cases than true-positive cases. After identifying relevant risk
groups that potentially may benefit from screening, it is necessary to prioritize those groups
with the highest risk. It is also necessary to choose the appropriate screening and diagnostic
tests and algorithms for each risk group and for each epidemiological situation.

1.5 Objectives of the operational guide

This document provides practical guidance on translating WHO’s principles and

recommendations for screening into a national or local strategy that sets out clear
objectives for screening, prioritizes risk groups, and defines the most appropriate screening
approaches. The following essential steps should be pursued:

1. the situation must be assessed;

2. the objectives of screening must be defined;
3. risk groups must be prioritized for screening;
4. screening algorithms and implementation approaches for each risk group must be
chosen;
5. a budgeted implementation plan must be developed;
6. the strategy must be monitored and evaluated.

These six steps form a cycle of assessing, planning, implementing, monitoring and evaluating
the programme, which then leads to revising the strategy and updating the implementation
as necessary. Thus, these six steps are an iterative process that should be continually
followed throughout screening and integrated with overall national TB and health systems
activities (Figure 1).

6
Figure 1. The six essential steps in the cycle of designing and implementing a tuberculosis
screening programme

7
 6, 15
Box 1. Principles of and recommendations for systematic screening for tuberculosis (TB)

Key principles of systematic screening for active TB

The following key principles should be considered when planning a TB-screening strategy.

1. Before screening is initiated, high-quality TB diagnosis, treatment, care, management and

support for patients should be in place, and there should be the capacity to scale these up
further to match the anticipated rise in case detection that may occur as a result of
screening. In addition, a baseline analysis should be completed in order to demonstrate that
the potential benefits of screening clearly outweigh the risks of doing harm, and that the
required investments in screening are reasonable in relation to the expected benefits.

2. Indiscriminate mass screening should be avoided. The prioritization of risk groups for
screening should be based on assessments made for each risk group of the potential
benefits and harms, the feasibility of the initiative, the acceptability of the approach, the
number needed to screen, and the cost effectiveness of screening.

3. The choice of algorithm for screening and diagnosis should be based on an assessment of
the accuracy of the algorithm for each risk group considered, as well as the availability,
feasibility and cost of the tests.

4. TB screening should follow established ethical principles for screening for infectious
diseases, observe human rights, and be designed to minimize the risk of discomfort, pain,
stigma and discrimination.

5. The TB screening approach should be developed and implemented in a way that optimizes
synergies with the delivery of other health services and social services.

6. A screening strategy should be monitored and reassessed continually to inform re

prioritization of risk groups, re-adaptation of screening approaches when necessary and
discontinuation of screening at an appropriate time.

Recommendations on risk groups to screen

Seven recommendations on prioritizing risk groups for screening have been developed. The
recommendations are divided into strong recommendations and conditional recommendations.

A strong recommendation is one for which the desirable effects of adhering to the recommendation
are judged to clearly outweigh the undesirable effects, and for which screening is judged to be
feasible, acceptable and affordable in all settings.

A conditional recommendation is one for which the desirable effects of adhering to the
recommendation probably outweigh the undesirable effects but the trade-offs, cost effectiveness,
feasibility or affordability, or some combination of these, are uncertain. Reasons for uncertainty may
include:

x a lack of high-quality evidence to support the recommendation;

x high costs or low feasibility or acceptability, or a combination of these.

8
Strong recommendations

Recommendation 1: Household contacts and other close contacts should be systematically screened
for active TB.

Recommendation 2: People living with the human immunodeficiency virus (HIV should be
systematically screened for active TB at each visit to a health facility.

Recommendation 3: Current and former workers in workplaces with silica exposure should be
systematically screened for active TB.

Conditional recommendations

Recommendation 4: Systematic screening for active TB should be considered in prisons and other
penitentiary institutions.

Recommendation 5: Systematic screening for active TB should be considered in people with an

untreated fibrotic chest X-ray lesion.

Recommendation 6: In settings where the TB prevalence in the general population is 100/100 000
population or higher, systematic screening for active TB should be considered among people who
are seeking health care or who are in health care and who belong to selected risk groups.

Recommendation 7: (a) Systematic screening for active TB may be considered for geographically
defined subpopulations with extremely high levels of undetected TB (1% prevalence or higher). (b)
Systematic screening for active TB may be considered also for other subpopulations that have very
poor access to health care, such as people living in urban slums, homeless people, people living in
remote areas with poor access to health care, and other vulnerable or marginalized groups,
including some indigenous populations, migrants and refugees.

9
 2. The six steps of the planning and implementation cycle

2.1 Assessing the situation

The specific epidemiology of TB in each setting as well as the social and the health-system
contexts will inform decisions on a TB screening strategy, including how risk groups are
prioritized, which screening approach is chosen, and whether screening in specific risk
groups is feasible. Therefore, before embarking on detailed planning, it is essential to
undertake a baseline assessment of the following features:
x the epidemiology of TB – to identify gaps in case detection, current case-finding
activities and the size and distribution of risk groups that might be targeted for
screening;
x the social setting – to assess if screening in specific communities or risk groups can
be advised given acceptability, safety and stability of the community;
x the national TB programme and the general health-care system – to assess their
preparedness for pursuing screening and health worker and facility capacity to
manage a potential increase in evaluating, diagnosing, monitoring and treating
patients with TB and referral of persons identified with symptoms of other
respiratory ailments/health conditions identified during TB screening;
x the coverage and rights of those screened for and those ill with TB – to ensure that
all people diagnosed with TB have access to high-quality care and to ensure that they
are protected from undue harm as a result of their diagnosis or due to the screening
process.

There are two complementary approaches for improving the early detection of TB (Figure 2):
1. enhancing the patient-initiated pathway to TB diagnosis; and
2. utilizing the provider-initiated screening pathway to TB diagnosis.16

Figure 2. Comparison of patient-initiated and provider-initiated screening pathways for the

diagnosis and treatment of tuberculosis (TB)

10
2.1.1 Assessing the potential to enhance the patient-initiated pathway to TB diagnosis

The primary approach to enhancing case detection is to optimize the patient-initiated

pathway to TB diagnosis and treatment. This foundational approach to providing health care
may be supplemented in clearly identified settings by systematic screening as a secondary
approach along a provider-initiated pathway. However, the potential for enhancing early
case detection by improving the patient-initiated pathway should be assessed first, and this
assessment should include the potential benefits of:
x improving access to care – including reducing the direct and indirect costs to
patients associated with seeking care, as well as addressing the specific needs of
vulnerable groups by strengthening primary health-care services, providing
additional outreach services that cater to these populations, and providing social
protection schemes where possible and needed;
x community engagement and demand generation – education and awareness
campaigns in communities that are at a higher risk of TB can increase the
likelihood that those with prevalent active disease will seek care for their illness
at facilities with the capacity to diagnose and treat TB;
x health-system strengthening – providing additional training and equipping all
health-care workers across the health system, including those working in the
public and private sectors and lay community workers and volunteers,17 will
increase the likelihood that patients with symptoms of TB who seek care are
recognized and referred for appropriate evaluation and care;
x reassessing the definition of a person suspected of having TB – broadening the
indications for diagnostic testing for TB, in accordance with the local
epidemiology of the disease and the epidemiology of the most common risk
factors for TB, can help ensure that the appropriate people are targeted for
evaluation
x making any other changes to the current algorithm for passive case-finding –
since such changes may result in a higher yield of patients identified in facilities.
Greater use of chest radiography , Xpert MTB/Rif (see below), and other tools
may increase the sensitivity of the algorithm while achieving acceptable
specificity.

Additional approaches to increasing the capacity for TB care and prevention include:
x scaling up the Practical Approach to Lung Health;18
x improving the quality of sputum-smear microscopy;
x improving the diagnosis of smear-negative TB, extrapulmonary TB and TB in
children;19
x introducing and scaling up new WHO-approved diagnostics, such as the Xpert
MTB/RIF assay20 (Cepheid, Sunnyvale, CA);
x providing access to chest radiography services; and
x improving referrals and notifications among all care providers.17

11
 2.1.2 Assessing the potential for screening for TB in high-risk groups

Screening for active TB is a relevant complement to improving early TB detection in specific

groups that are at high risk of TB or have poor access to TB services, or both. The following
risk groups should always be systematically screened for TB:
x close contacts of people with TB;
x people living with HIV; and
x people exposed to silica (mainly some types of miners).

When assessing the situations of the three risk groups highlighted above, the focus should
be on how to screen, not if to screen. The assessment of these groups should include the
size and distribution of the group, the TB burden within the group, the past and current
screening experiences, and any remaining considerations and challenges that will need to be
addressed to optimize the screening efforts.

For other risk groups (see Table 1) screening may or may not be appropriate. In most
settings it is relevant to consider only a few additional risk groups than those listed above. In
some settings, no additional risk groups should be considered. In order to develop a rational
screening strategy, there is a need to assess the relevance and potential cost and cost-
effectiveness of systematic screening in each potential risk groups (see section 2.3,
Identifying and prioritizing risk groups).

Table 1. Possible risk groups to consider when screening for tuberculosis (TB) 6
Potential site of screening Risk group
Community Geographical areas with a high prevalence of TB
Subpopulations with poor access to health care and with other
associated risk factors (such as living in a poor or a remote
area; being a member of an indigenous or tribal population;
being a migrant, refugee, homeless, or nomadic)
Hospital outpatient and inpatient People previously treated for TB
departments, and primary health- People with an untreated fibrotic chest radiography lesion
care centres People living with HIV / People attending for HIV testing
People with diabetes mellitus
People who smoke / People with chronic respiratory disease
Undernourished people
People who have had a gastrectomy or jejunoileal bypass
People with an alcohol-use disorder / Injection drug users
People with chronic renal failure
People on treatments that compromise their immune system
Elderly people
People in mental health clinics or institutions
General outpatients/inpatients
Residential institutions Prisoners and prison staff
People residing in shelters
Other congregate institutions (such as the military)
Immigration and refugee services Immigrants from settings with a high prevalence of TB
People in refugee camps
Workplaces Health-care workers
Miners or others who are exposed to silica
Other workplaces with a high prevalence of TB

12
2.1.3 Assessing gaps in TB case detection, challenges to screening, and entry points for
interventions

The main purpose of conducting a situation assessment is to identify gaps in TB case

detection and opportunities for addressing those gaps through screening. This assessment
must consider the potential benefits, risks and costs of systematic screening, particularly in
relation to other possible interventions.

The analysis needs to be disaggregated by age, sex and geographical location, and special
attention should be paid to vulnerable groups that are at high risk of TB or likely to face
barriers to accessing TB services, or both.

The specific questions that should be addressed in a situation assessment are shown in
Table 2. The web-based tool described in section 3 further highlights what quantitative
baseline information is required to estimate potential yield and cost of screening. It is
therefore advisable to use the web-based tool as a starting point for the assessment, while
obtaining the additional information that need to be imputed in the tool.

Potential data sources include:

x surveillance data;
x data from prevalence surveys;
x evaluations of previous or continuing activities to improve case-finding and
screening;
x national health and demographic statistics;
x findings from research studies.

Useful information on collecting and interpreting data can be found in:

x WHO’s Tuberculosis prevalence surveys: a handbook;21
x WHO’s guidance on Understanding and using tuberculosis data;22
x WHO’s Framework for conducting reviews of tuberculosis programmes; 23
x WHO’s Public–private mix for TB care and control: a tool for national situation
assessment;24
x WHO’s ENGAGE TB: integrating community-based tuberculosis activities into the
work of nongovernmental and other civil society organizations. Operational
guidance;25
x The tool to estimate patients’ costs;26
x WHO’s guidance on Contributing to health system strengthening - Guiding principles
for national tuberculosis programmes.27

13
 Table 2. Questions to be addressed when conducting a situation assessment before
implementing screening for tuberculosis (TB)
Area to be assessed Questions to be explored

Distribution of TB x What is the current distribution of the TB burden in this setting (in terms of
burden; size and notification, prevalence and mortality), and specifically for different
distribution of gaps in subpopulations or risk groups?
case detection x What is the current gap in case detection, and what are the specific causes
of delays in diagnosis for each subpopulation or risk group?
x Which subpopulations or risk groups have the highest risk of TB remaining
undetected?
x Which types of TB are most likely not to be detected? (extrapulmonary,
smear-negative TB, etc.)
x What are the main reasons for gaps remaining in case detection?
Current case-detection x What is the level of knowledge about TB among health-care staff and others
activities who provide care?
x What is the current definition of suspected TB, and to what extent is it
applied in practice?
x Which diagnostic tests and algorithms are used to screen for and diagnose
different types of TB?
x To what extent has Xpert MTB/RIF (or other rapid molecular tests) been
scaled up, and which individuals are eligible?
x Are chest X-rays available? Are they of good quality? Are the interpretations
of the chest X-rays of good quality? How are chest X-rays used for TB
screening and diagnosis?
x What is the trend in the number of people being tested for TB, by
subpopulation?
x What is the trend in the proportion of people testing positive for TB among
those tested, by subpopulation?
Role of different x What are the common health-seeking patterns?
providers x From which providers do people usually seek care first?
x What diagnosis and treatment services are offered by different providers
(for example, in the public and private sectors; among formal or informal
providers; by health-care or other providers; by community or civil society
organizations)?
x What are patients’ previous experiences of engaging with different health-
care providers, communities or civil society organizations?
TB awareness and health x What barriers prevent access to diagnostic and treatment services among
seeking the targeted community?
x What is the level of knowledge about TB and TB care in the targeted
community?
x What are the main reasons for delays in seeking health care among the
targeted community?
Risk group size, x What is the size and geographical distribution of the different TB risk groups
distribution, and special (Table 1)?
challenges x Which specific barriers to accessing care affect the different groups?
x What are the specific challenges to initiating and adhering to treatment in
each group?
Previous and present x What were the results of any previous efforts to improve the patient-
experiences in improving initiated pathway to enable earlier detection of TB?
early TB detection x What were the outcomes and lessons learnt from previous systematic
screening initiatives in different risk groups?

14
2.1.4 Assessing the national TB programme and the preparedness of the health-care
system

High-quality services for TB diagnosis, treatment and management, as well as support

services for patients, should be in place before systematic screening for active TB is pursued.
This will minimize the risks of any negative effects from screening, including the risk of a
false-positive diagnosis and the accompanying anxiety, unnecessary treatment and delay in
receiving an appropriate diagnosis (especially if the quality of TB diagnostic services are
suboptimal) or worsening of TB treatment outcomes (if treatment services are suboptimal
and not properly tailored to specific vulnerable groups that may be targeted through
screening). Moreover, implementing systematic screening in a context of poor-quality
general services raises ethical concerns, and may lead to a loss of confidence in the services
provided among the population served. In addition, the capacity of specific health
institutions and health staff to take on additional functions related to TB screening needs to
be carefully assessed, so as not to undermine the quality of TB and other services.

The critical conditions that must be met before systematic screening is implemented include
ensuring that:
x quality-assured diagnostic services are available;
x regular and reliable supplies of anti-TB medicines are available and there is the
capacity to treat the anticipated rise in cases of drug-susceptible as well as drug-
resistant cases among adults and children;
x there is a low rate of initial loss to follow-up;
x the success rate of treatment is adequate and the rate of overall loss-to-follow-up is
low;
x there are sufficient mechanisms to provide support for diagnosed patients, and
there is capacity to tailor treatment programmes to the specific needs of the
population that will be screened;
x if the Xpert MTB/RIF assay or other tests are used to assess drug resistance, there is
adequate capacity for culture testing and drug-susceptibility testing and for
programmatic management of drug-resistant TB;
x adequate financial resources and human resources can be made available for
screening without adversely affecting other key functions of the health-care system.
Primary and auxiliary health staff may be the most affected if their duties are
expanded to take on screening functions at health services or in community settings
without planning to ensure that other work is not foregone or their workloads
become unmanageable. Supervision of screening efforts also requires capacity-
building and time.

For most risk groups, systematic screening for TB should involve collaboration with other
health and social programmes, which may already be engaged in screening the targeted
population for other conditions. Thus, outreach activities focusing on health promotion or
providing social support for vulnerable and hard-to-reach populations may already be in
place. These may serve as platforms for TB screening within a broader, more integrated
approach to outreach. The analysis of the situation should include mapping the screening
and outreach activities that may be relevant, and assessing other programmes’ potential

15
 and readiness for intersectoral collaboration; this assessment will be important for making
judgements about feasibility, costs and cost effectiveness of screening.

Table 3 highlights the programmes, services and stakeholders that could collaborate on
screening activities.

The following key questions must be answered when considering whether to develop an
intersectoral collaborative screening programme with other providers of health-care or
welfare.

x Which health conditions are already being screened for?

x What links exist among health-care services?
x Do any of the potential collaborating agencies have experience screening for TB?
x Is there capacity to include TB screening?

Table 3. Services, programmes and stakeholders that could collaborate with systematic
screening programmes for tuberculosis (TB)

Services Programmes and stakeholders

Health services x HIV programmes, clinics offering voluntary counselling and testing for HIV, clinics
delivering antiretroviral therapy, programmes aimed at preventing mother-to-child
transmission of HIV
x Diabetes or endocrinology clinic screening initiatives, undertaken within the broader
platform of preventing noncommunicable diseases
x Maternal and child health and antenatal care programmes
x Alcohol and drug-abuse clinics and their outreach programmes
Social services x Outreach and community support or development programmes in remote rural areas or
urban slums; programmes targeting homeless people and other vulnerable populations
x Programmes providing social support for sex workers
x Programmes providing social services for immigrants and refugees
x Social protection schemes for poor people
x Food support programmes
x Other partner agencies working with affected or vulnerable populations
Other government x Prison health services
services
x Occupational health services (especially those targeting workers in mines, health-care
workers and workers in other high-risk occupations)
x Migration authorities
Civil society x Nongovernmental organizations or others providing social support for vulnerable
organizations groups
Private health-care x Private providers
providers
x Informal providers

16
2.1.5 Assessing policies on health-care coverage and frameworks for legal and human
rights

TB screening carries both opportunities and risks for the individual. Before screening is
started, it is essential to ensure that people who are diagnosed with TB have the right to
high-quality TB care. This may not be the case for certain vulnerable groups, such as
migrants, refugees, and homeless people, who may lack identity papers or health insurance.
Inclusion criteria for screening, coverage of health insurance (where applicable) and access
to health services need to be assessed.

Discrimination against key affected populations – such as sex workers; injection drug users;
and some ethnic minorities – can severely hamper access to treatment, and this may be
reinforced by a lack of a framework for human rights. The existing frameworks for
protecting human rights, and the extent to which they are enforced, must be reviewed
before systematic screening is implemented.

The possible stigmatization of and discrimination against people screened for TB and people
diagnosed with TB can create risks for people undergoing screening. For example, people
who are diagnosed with TB may lose their jobs temporarily or permanently, or be expelled
from school or forced to divorce. Migrants may face deportation. The risks of discrimination
and stigmatization should be carefully assessed prior to initiating screening. In particular,
the legal status of migrants needs to be fully understood and considered when designing the
screening plan, both with regards to their access to health services and the risks of
expatriation if they are diagnosed with TB. Similarly, when specific occupational groups are
screened, the legal protections of rights to care and the right to maintain employment must
be considered.

2.2 Setting goals and specific objectives

The goals and specific objectives of screening depend on what targets have been set and
what gaps have been identified by the situation assessment. Generally, the primary
objective of screening is to detect active TB early in order to contribute towards two
ultimate goals:
1. reducing the risk of poor treatment outcomes, health sequelae and the adverse social
and economic consequences of TB for individuals with the disease. This reduces
suffering, the prevalence of TB and death from TB;
2. reducing TB transmission by shortening the duration of infectiousness. This reduces the
incidence of TB infection and consequently contributes to a reduced incidence of TB
disease.

When goals and targets are set, it is important to ensure that there is equitable access to
diagnosis and treatment, which implies that the groups that are most difficult to reach
should be prioritized in screening.

A second objective can be to rule out active disease to help identify people who are
eligible for treatment of latent TB infection, such as people living with HIV and close

17
 contacts of TB patients who are younger than 5 years. For further information on screening
and managing latent TB infection, see WHO’s Guidelines on the management of latent
tuberculosis infection.28

Furthermore, screening can help identify people who are at particularly high risk of
developing active disease and thus may require repeat screening. For example, people
with an abnormal chest X-ray that is compatible with TB but who were not diagnosed with
active disease at the time of screening may benefit from repeat screening in the future.

Combining screening for TB with screening for TB risk factors (such as HIV, diabetes
mellitus, chronic obstructive pulmonary disease, low body mass index or smoking) can also
help map individual or community-level risk factors and socioeconomic determinants that
need to be addressed to more effectively prevent the disease. This may be an additional
objective in settings where information about the prevalence and distribution of TB risk
factors is lacking.

2.3 Identifying and prioritizing risk groups

Indiscriminate mass screening should be avoided. Risk groups should be prioritized for
screening based on assessments of the potential benefits and harms in relation to costs,
which is a function of; total potential yield, the risk of a false positive diagnosis, the number
needed to screen (NNS) to detect a true case of TB, the potential impact on transmission,
the feasibility of the initiative and the acceptability of screening to the group. These
assessments should be made for each risk group.

A tool has been developed to assist with the process of prioritizing risk groups for screening.
The tool produces estimates of the potential yield of true and false positive TB and cost of
screening, according to the risk group(s) being targeted and the screening algorithm(s) being
used. See section 3 for a full description.

Three groups should always be systematically screened, namely:

x contacts of people with TB;
x people living with HIV; and
x people working in places where they are exposed to high levels of silica (mainly
some types of miners).

Other risk groups (Table 1) should be prioritized for screening based on the assessment of
the situation and on the goals and objectives of screening. When prioritizing groups to
screen, the factors described in sections 2.3.1–2.3.8 should be considered for each risk
group and in relation to the specific objectives of screening.

Prioritization may vary depending on which stakeholder is responsible for the screening
initiative. For example, a national TB programme under the auspices of a ministry of health
may have other mandates, priorities and resources than health services that are managed
by a ministry of justice, ministry of labour, an immigration authority, a nongovernmental
organization, a private health-care provider or an employer.

18
Systematically screening for active TB in children is problematic since both the screening
and diagnostic tools are less accurate in children than in adults and, therefore, there is a
higher risk of large number of diagnostic tests being required as well as a high risk of large
numbers of false-positive cases unnecessarily starting TB treatment. In principle, only
children who are close contacts of someone with TB and HIV-positive children should be
systematically screened for TB. Other children should be assessed according to diagnostic
algorithms for paediatric TB as part of standard clinical management practices.

2.3.1 Potential benefits for the individual

These benefits include the health, social and economic benefits of early diagnosis and
treatment. In principle, the potential benefits are greater for persons who are at the
highest risk of delayed diagnosis because there are barriers to them obtaining health care
(for example, people in poor communities, people living in remote areas) and especially
those who have the highest risk of poor treatment outcomes when diagnosis is delayed
(for example, because their immune system is compromised, such as people living with HIV).

2.3.2 Potential risks and harms for the individual

The screening procedure itself may be inconvenient and have direct and indirect costs for
the individual, and these may vary with both the risk group and the screening approach.
Harms associated with the results of screening include the unintended negative effects of
being correctly diagnosed (which may include stigmatization or discrimination) and the
harms caused by a false-positive or a false-negative diagnosis. Particular attentions should
be paid to these harms for groups such as migrants, who may risk deportation if TB is
diagnosed or suspected, and employees who lack legal protection against dismissal if they
are diagnosed with TB.

The risk of false positive diagnosis depends on both the prevalence of TB in the screened
group, as well as on the screening and diagnostic algorithm used. Screening in groups with
low TB prevalence can result in a large proportion with a false-positive result. Therefore, as
a general rule, screening should be avoided in low risk groups. The importance of choosing
an appropriate screening and diagnostic algorithm in order to minimize the number of false
positive outcomes is further discussed in section 2.4.

2.3.3 Potential to identify other conditions that need medical attention

When someone is screened for TB, other conditions that require treatment may be
identified (such as lung cancer or chronic obstructive pulmonary disease); offering
treatment for other conditions may not be within the scope of the screening team’s
responsibilities. Links must be developed with other health programmes to handle these
cases.

19
 2.3.4 Potential total yield of true TB cases

The potential total case-detection yield is a function of:

x the size of the risk group and the proportion of them that can be reached;
x the prevalence of TB in the risk group;
x the sensitivity of the screening approach; and
x the acceptance of screening in the risk group.

Figure 3 shows the potential yield of screening across a range of hypothetical risk groups
and across a range of relative risks of TB (assuming 100% coverage, acceptance to screening,
sensitivity and specificity of screening).

As illustrated in Figure 3, the yield of TB screening in a specific risk group (in terms of the
number of TB cases detected) is driven by both the size of the risk group (or the prevalence
of the risk factor in the general population) and the prevalence of TB within that risk group.

Figure 3. Potential yield of screening as a function of the prevalence of the risk factor in the
population and the relative risk of tuberculosis (TB) in the risk group (baseline incidence, 100
cases/100 000 in a population of 1 000 000)

4000
3500
Number of TB cases

3000
2500
2000
1500
1000
500 20
0 10
0.1% 5
0.5%
1.0% 3 Relative
5.0%
10.0% risk of TB
15.0%
20.0%
Prevalence of risk factor

Often, the groups at the highest risk of TB are also the smallest, and groups with only a
moderately elevated risk can be very large. For example, the population prevalence of HIV,
which is associated with up to 20-fold risk increase, is normally less than 1% (with the
exception of some countries in sub-Saharan Africa), and the total number of close contacts

20
of someone with TB (who also have a dramatically elevated TB risk) is normally a very small
fraction of the total population. However, risk factors such as having diabetes or
undernutrition, or living in a crowded slum, which normally have moderate relative risks for
TB (in the range of 2–3) could affect more than 10% of the total population.

Therefore, screening in the highest risk groups often gives a low total yield. A high overall
yield from screening may be possible only by achieving very high coverage of screening in
large groups that have a moderate increase in their risk of TB. However, screening in these
groups will have a higher NNS and cost per case detected than screening in groups at very
high risk. The risk of a false positive diagnosis is also higher in these groups. Therefore,
there will often be a difficult trade off between the desire to achieve a large total yield
and the cost effectiveness.

2.3.5 Potential impact on transmission within and beyond the risk group

The potential of screening to have an impact on transmission is theoretically highest in

congregate settings, such as prisons or overcrowded urban slums, where there is a high
rate of transmission and where there is also substantial in-migration and out-migration. In
principle, the larger the total yield of screening, the larger the potential impact on
transmission in the community. However, when the TB burden is highly concentrated in a
few high-risk groups, the largest impact on overall transmission may come from screening
carefully selected groups, and these may be small in size.

2.3.6 The number needed to screen to detect a case of TB

The NNS to identify one true case of TB in a specific risk group is the inverse of the
prevalence of detectable TB in that risk group, assuming 100% sensitivity of the screening
and diagnostic tools being used. If a given risk group has a very low prevalence of detectable
TB many people will have to be screened in order to find one case of TB, and this will
translate into a high NNS. However, if a given risk group has a high prevalence of TB that can
be detected by the screening and diagnostic tools being used, fewer people will need to be
screened for each case detected, resulting in a lower NNS. Figure 4 illustrates the idea of the
NNS in a risk group.

21
 Figure 4. The number needed to screen (NNS) to diagnose one case in any given risk group is
roughly the inverse of the prevalence of the disease in that risk group

Figure 5 shows the relationship between the prevalence of TB in a risk group (per 100 000
population) and the NNS, assuming 100% sensitivity and specificity in screening and
diagnosis. However, this assumption is never met and, therefore, the NNS will always be
higher in practice.

22
Figure 5. Number needed to screen (NNS) at different levels of tuberculosis (TB) prevalence,
assuming 100% coverage, sensitivity and specificity

2000
1800
1600
NNS to detect 1 case of TB

1400
1200
1000
800
600
400
200
0
100 200 300 400 500 600 700 800 900 1000
Prevalence of undetected TB per 100 000 population

As demonstrated in Figure 5, the NNS accelerates at lower levels of TB prevalence. At a

prevalence of 200/100 000 population the NNS is at least 500 (in practice, it will be higher
when the sensitivity of the screening is suboptimal). The prevalence of undetected TB in the
general population is often less than 200/100,000, even in countries with the high burden of
TB and, therefore, screening the general population is not usually cost effective.

The NNS is a rough indicator of cost effectiveness and of effort. Comparing the NNS across
risk groups provides a measure of relative cost effectiveness if it can be assumed that the
cost of screening and treatment, as well as the benefits of early treatment, are the same
across risk groups (however, this is rarely the case).

In order to guide the prioritization of risk groups the NNS should be estimated for each
group being considered for screening, and it should be specific to the screening algorithms
being used. This process is described in detail in section 3.

2.3.7 Feasibility of identifying, reaching and screening people, and having them start and
complete treatment, and the acceptability of screening in a risk group

The feasibility and acceptability of screening need to be assessed in relation to both those
who will be screened and those who will provide screening.

Certain risk groups will be harder to reach than others. To some extent, the structure of
health and social services will determine which risk groups can be reached most easily.

23
 Generally, it is more feasible to conduct screening in well defined risk groups that can be
reached in a specific location, such as clinical risk groups that can be identified within health
facilities, people who are living in institutions (such as prisons) and people working in high-
risk locations (such as mines).

Some people may accept screening more readily than others, depending on the perceived
cost and inconvenience of screening as well as the adverse consequences of a TB diagnosis
(such as stigmatization or discrimination), compared to the perceived benefits. The
reported acceptance rates of screening for different risk groups are available in the web
annexes.

Whether screening will be accepted depends on how the programme is designed and
implemented, and, therefore, it is difficult to predict based on evidence from previous
programmes. The acceptability of screening models may be assessed in advance by
organizing focus groups of target populations that, preferably, have an age and sex
distribution that matches the populations at highest risk.

2.3.8 Cost–effectiveness and cost–benefit ratios

Pre-implementation, the cost effectiveness of the programme can be modelled based on

estimates of the predicted number of additional true TB cases detected, the reduction in
morbidity, the reduction in time that a person remains infectious, and the reductions in
transmission, incidence and mortality.

The cost–benefit ratio can be estimated in terms of future costs saved for the individual, the
health sector or society, or all of these. The total cost depends on the NNS, the algorithm
used for screening and diagnosis, the method used to reach people for screening, and the
direct and indirect costs incurred by the screened individuals.

To properly determine the cost effectiveness of screening in relation to its impact on public
health it is necessary to conduct intervention trials that collect appropriate data on costs of
screening interventions as well as data on the epidemiological impact. Such data are unlikely
to be available in the foreseeable future in many settings. However, models can be used to
estimate how costs relate to the potential impact on TB transmission and epidemiology.
Nonetheless, because there is no good empirical evidence about the impact of screening on
transmission, such models will be highly speculative. In the interim, section 2.3.9 describes
how basic cost effectiveness – that is, the cost per case detected through screening – can be
estimated using the tool for prioritizing risk groups described below.

24
2.4. Choosing algorithms for screening and diagnosis

2.4.1 Algorithm options

An algorithm for systematic screening should combine one or several screening tests and
one or several diagnostic tests. Screening tests should distinguish between people with a
high likelihood of having active TB and people who are unlikely to have active TB. A
screening test is not intended to be diagnostic but rather to identify the subgroup of people
with the highest likelihood of disease. People with positive results on a screening test then
undergo diagnostic evaluation to bacteriologically confirm or rule out active TB. A negative
diagnostic test may have to be followed up with clinical evaluation (mainly based on chest
radiography, symptoms and medical history). A positive diagnostic test result may have to
be re-confirmed with further testing and clinical evaluation if the positive predictive value
(PPV) of the test result is low. The tool described in section 3 can help in selecting an
appropriate algorithm.

WHO’s guidelines on systematic screening for active TB6 includes 10 screening algorithm
options, consisting of a combination of one or two screening tests and a diagnostic test
(Annex). The algorithms have been developed predominantly to detect pulmonary TB. The
accuracy of the tests has been assessed using culture-confirmed pulmonary TB as the gold
standard. While culture is the gold standard for diagnostic testing for TB, in these algorithms
it is not considered as an initial diagnostic test because it demands more resources and
requires a much longer wait for results (2–8 weeks) than both the Xpert MTB/RIF test and
sputum-smear microscopy, both of which can provide results in less than 1 day. Where
resources permit, and where the health system has sufficient capacity to ensure that
patients are followed up after culture results are available, culture may be used in parallel
with or after testing with the Xpert MTB/RIF assay or sputum-smear microscopy.20
Specimens should undergo culture and drug-susceptibility testing according to the
guidelines for diagnosing drug-resistant TB.29

The algorithms each have different sensitivity and specificity, and, therefore, different
potential yields of true-positive and true-negative cases and false-positive and false-
negative TB. Yields also vary with the prevalence of TB in the population being screened. For
all algorithms, the risk of a false-positive diagnosis increases as the prevalence declines;
therefore, special attention must be paid to diagnostic accuracy, particularly when the
prevalence of TB in the screened population is less than 1%. At a TB prevalence of 0.5% in
the screened population, all of the algorithms have a PPV of less than 75% (i.e. 25% have a
false positive diagnosis) when clinical diagnosis is used for all or some of those with a
negative result from their initial diagnostic test. Even when clinical diagnosis is not
considered, the PPV is below 80% for all but one algorithm. Special efforts must therefore
be made to ensure high quality of diagnostic procedures and clinical assessment especially
when TB prevalence in the screened population is moderate to low.

For each given screening situation it is critical to consider what proportion of false positive
and false negative results are unacceptable. Ethical considerations should guide the
permissible sensitivity and specificity of the algorithm. Considerations will vary across risk

25
 groups. Especially in groups with a high risk of severe negative effects from missed or
delayed diagnosis and treatment, it is important to use an algorithm that has very high
sensitivity, although this often leads to lower specificity.

The algorithms have different costs and requirements in terms of human resources and
health systems. Which algorithm is chosen for screening and diagnosis depends on the risk
group, the prevalence of TB, the availability of resources and the feasibility of implementing
the algorithm.

Screening tests
Some commonly used initial screening tests include:
x screening for cough lasting for longer than 2 weeks;

x screening for any symptom compatible with TB, including –

o cough of any duration
o haemoptysis
o weight loss
o fever
o night sweats;

x screening with chest radiography.

If symptom screening is used initially, then chest radiography can be used as a second
screening to improve the pretest probability of the subsequent diagnostic test and to
reduce the number of people who need to undergo a full diagnostic evaluation.

26
Diagnostic tests
Each screening algorithm also includes one of two options for diagnostic testing for people
who screen positive:
x sputum-smear microscopy; or

x a rapid molecular test that has been demonstrated to have high accuracy for both
smear-positive and smear-negative pulmonary TB, such as the Xpert MTB/RIF test or
any rapid test recommended by WHO in the future that has the same or better
accuracy.

Screening algorithms and people living with HIV

As part of the initial screening, each algorithm seeks to identify people living with HIV; these
people should be screened and diagnosed by following the algorithm in WHO’s Guidelines
for intensified tuberculosis case-finding and isoniazid preventive therapy for people living
with HIV in resource-constrained settings.30 Screening can be enhanced by combining
screening for TB with screening for HIV, especially in settings with a high burden of HIV.30 In
settings with a low prevalence of HIV, it is normally sufficient to ask a patient about their
HIV status.

27
 2.4.2 How to choose an algorithm for a particular risk group

The choice of screening and diagnostic algorithms should be based on:

x the specific objectives of screening,
x the accuracy and yield of the screening and diagnostic tests,
x the profile of the prioritized risk groups,
x the TB prevalence in the risk groups,
x the cost, availability and feasibility of using different tests, and
x the ability to engage the population to be screened.

Specific objectives of screening

The specific objectives of screening will partly determine the relative importance of the
sensitivity of the algorithm compared with its specificity, as well as the trade off between
cost and yield or potential epidemiological impact. For example, if one objective is to
determine eligibility for treatment for latent TB (for example, as part of an investigation of
contacts), then it is critical to have very high sensitivity (and thus very high negative
predictive value of a negative result) but suboptimal specificity may be acceptable (which in
this case might lead to treating people for active TB rather than latent TB). In other
situations it may be critical to avoid false-positive diagnoses, and a less sensitive but highly
specific algorithm may be preferable.

Accuracy and yield of screening and diagnostic tests

Table 4 and Table 5 summarize the published sensitivity and specificity of the screening and
diagnostic tests as of 2012 described in section 2.4.1. Table 4 shows the modelled yield of
screening in a population with a 1% prevalence of TB using different algorithms.

Table 4. Pooled sensitivity and specificity of different screening tools for pulmonary
tuberculosis (TB) using culture-confirmed pulmonary TB as the gold standard6

Screening tool Pooled sensitivitya Pooled specificitya

Chest radiography
Any abnormality compatible with TB (active 98 (95–100) 75 (72–79)
or inactive)
Abnormalities suggestive of active TB 87 (79–95) 89 (87–92)
After positive screening for symptoms (any 90 (81–96) 56 (54–58)
abnormality)b
Symptom screening
Prolonged cough (lasting >2–3 weeks) 35 (24–46) 95 (93–97)
Any cough 57 (40–74) 80 (69–90)
Any TB symptom (in settings with a low 70 (58–82) 74 (53-95)
prevalence of HIV)
Any TB symptom (in settings with a high 84 (76–93) 61 (35-87)
prevalence of HIV)
Any TB symptom (in settings with a low 77 (68–86) 68 (50–85)
prevalence or high prevalence of HIV)
a
Values are % (95% confidence interval).
b
Results from only one study; data are for any abnormality seen on chest radiography.

28
Table 5. Pooled sensitivity and specificity of different diagnostic tests for tuberculosis (TB),
from systematic reviews using culture-confirmed pulmonary TB as the gold standard6

Diagnostic test Pooled sensitivitya Pooled specificitya

Liquid culture (gold standard) 100 100

b
Conventional sputum-smear microscopy 61 (31–89) 98 (93–100)
Xpert MTB/RIF assay 92 (70–100) 99 (91–100)
Clinical diagnosis 24 (10–51) 94 (79–97)
a
Values are % (95% confidence interval).
b This refers to conventional light microscopy used to examine direct smears stained with Ziehl–Neelsen. Fluorescence
microscopy, including microscopy with light-emitting diodes generally has higher sensitivity than conventional light
microscopy.

Table 6. Modelled yield of different algorithms when screening 100 000 persons in a
population with a 1% prevalence of culture-positive pulmonary tuberculosis (TB) (1 000
cases). (It is assumed that final diagnosis uses results from sputum-smear microscopy or
the Xpert MTB/RIF test, and there is no further diagnostic evaluation)a 6

Outcome of diagnosis in persons with

Outcome of screeninga
Final positive screeninga
Screening test diagnostic TN FN NPV
b
Screened
d
TP Detected of FP PPV TN FN
e f
NPV
g
c
test (%) positive true (%) (n) (%)
cases
(%)
Cough lasting >2 weeks SSM 93 753 649 99.3 5 598 214 21 105 67.1 5 142 137 97.4
Xpert 93 753 649 99.3 5 598 324 32 52 86.0 5 195 27 99.5
1st screen: cough >2 weeks SSM 96 691 684 99.3 2 625 193 19 46 80.7 2 263 123 94.8
2nd screen (if 1st screen
positive): chest radiography Xpert 96 691 684 99.3 2 625 291 29 23 92.7 2 286 25 98.9
Any TB symptom SSM 67 023 230 99.7 32 747 470 47 640 42.3 31 337 300 99.1
Xpert 67 023 230 99.7 32 747 710 71 320 68.9 31 657 60 99.8
1st screen: any TB symptom SSM 84 930 307 99.6 14 763 423 42 281 60.0 13 788 270 98.1
2nd screen (if 1st screen
positive): chest radiography Xpert 84 930 307 99.6 14 763 639 64 141 82.0 13 929 54 99.6
Chest radiography: SSM 88 506 132 99.9 11 362 529 53 210 71.6 10 284 339 96.8
abnormality suggestive of
active TB Xpert 88 506 132 99.9 11 362 800 80 105 88.4 10 389 68 99.4
Chest radiography: any SSM 74 646 22 100.0 25 332 597 60 487 55.1 23 867 381 98.4
abnormality compatible with
TB Xpert 74 646 22 100.0 25 332 902 90 244 78.7 24 110 76 99.7
TN, true negative; FN, false negative; NPV, negative predictive value; TP, true positive; FP, false positive; PPV, positive
predictive value; SSM, sputum-smear microscopy; Xpert, Xpert MTB/RIF test.
a
Values are numbers unless otherwise indicated.
b
The negative predictive value for screening is the likelihood that someone whose screening test is negative does not have
TB.
c
This is the number of people whose screening test would be positive, which equals the number of people who should
have the diagnostic test
d
The positive predictive value is the likelihood that a person with a final diagnosis of TB has true culture-positive TB. It
summarizes the specificity and sensitivity of the entire algorithm, not just the diagnostic part.
e
The number of true negatives among people whose screening test is positive is the number of people correctly diagnosed
as not having TB among those whose screening test is positive and who have a diagnostic test.
f
The number of false negatives among people whose screening test is positive is the number of people falsely diagnosed as
not having TB among those whose screening tests are positive and who have a diagnostic test.
g
The negative predictive value for diagnosis among people whose screening test is positive is the likelihood that a person
whose screening test is positive and who is not diagnosed with TB does not have culture-positive TB.

29
 Profile of the prioritized risk groups
The profile of the risk group can influence the choice of algorithm because the accuracy of
certain tools is affected by underlying biological factors associated with certain risk factors
(for example, chest X-rays, Xpert and sputum-smear microscopy have lower sensitivity in
people living with HIV).

TB prevalence in the risk groups

The prevalence of TB in a risk group has a direct impact on the predictive values of all tests
and, therefore, on the yield of true-positive and false-positive cases and true-negative and
false-negative cases. The lower the prevalence, the more important it is for the algorithm to
have very high specificity in order to avoid a high proportion of false-positive cases.

Cost, availability and feasibility of using different tests

The total cost of an algorithm depends on the unit cost of each test (including both start-up
costs and running costs), the total number of tests required and the overhead costs for
delivering the services. Different algorithms require different numbers of different tests for
any given population with any given TB prevalence.

Table 6 provides estimated number of tests required for different algorithms, and displays
these inputs in relation to outputs in terms of case-detection yield. The tool described in
section 3 can be used to generate cost estimates for each algorithm and risk group based on
local cost assumptions. This information can be used to conduct a simple cost–effectiveness
analysis that focuses on the cost per true case detected.

However, the availability, cost and feasibility of tests may vary considerably in different
parts of the health-care system. Outreach screening requires special considerations with
regards to mobility and field conditions. For example, digital chest X-ray technology offers
lower running costs and higher mobility than conventional chest X-ray, but requires high
initial investment costs. Symptom screening may be relatively low cost, especially in
integrated services, but it also has low sensitivity. Sputum examination (either by smear
microscopy or using the Xpert MTB/RIF assay) may become more feasible under outreach
conditions if proper sputum collection and transportation can be organized.

Ability to gain access to the population to be screened

Although the algorithm used in the population that is screened will have significant
implications for the budget and logistics, so too will the approach that is used to conduct the
screening. Implementing contact investigation may require home visits or it can be done by
requesting that individuals with TB bring their contacts to a health facility to be tested.
Although the latter option may be far cheaper, the number of people actually screened may
be far smaller. Similarly, community outreach may involve setting up mobile treatment
teams and laboratories, engaging in home visits or simply using loudspeakers to announce
the availability of testing services. Different approaches work differently in different settings,
and their impact will vary depending on the number of people reached and tested, and on
the yield.

30
2.5 Planning, budgeting and implementing

2.5.1 Requirements for planning, human resources, commodities and budgeting

As noted in the assessment section, consideration should be given to the extra resources,
both human and financial, that will be needed to prepare for, carry out, and monitor
screening, and to accommodate the extra cases that may be identified by screening.

Determining which cadre(s) of staff will be involved in screening will require review of the
current terms of reference, workload and capacity of different staff, including supervisory
staff and staff enabling provision of commodities for the front-line screening workers.
Lessons should be assessed from other programmatic experience in screening within health
facilities as well as outreach efforts. The model of staffing and supervision can be highly
context-specific (even within countries), and could vary between urban and rural settings
and risk groups targeted.

New forms or registers may be required and training will certainly be needed. Screening can
be conducted by a variety of personnel, depending on which tests are being used. For
instance, symptom screening can be conducted by community health workers or volunteers.
Also, new diagnostic equipment or additional reagents and tests may be required for the
additional activities. In many cases, the logistics of gaining access to and testing the target
population will also require significant resources. Finally, if one of the goals of screening is
to increase the number of people beginning treatment, it will be important to ensure that
there is an adequate supply of medicines; it will also be important to ensure that patients
receive adequate support during treatment.

2.5.2 Choosing a screening programme model

The choice of screening programme will have implications for the resources required and
the potential reach and effectiveness of the programme. The decision about which model to
use should be based on determining which approach will be most effective at reaching the
targeted risk group with the resources available.

Programmes that conduct screening in locations where people gather for other purposes,
such as health centres or workplaces, can limit the effort and resources required to reach
the target population. However, not all populations can be reached using this method.

31
 • Screening health centre attendees

• Workplace screening

Programmes that bring screening to places where people live or work can reach more
vulnerable populations, particularly those for whom there are barriers to accessing care, but
these programmes require more resources. Such programme models can include home
visits, mobile outreach screening campaigns and community-based screening events, such
as health fairs.

• Screening in the home

32
• Mobile outreach screening campaign

• Community-based screening events (health fairs)

2.5.2 Ethical considerations

Ethical issues should be considered from the onset of the planning process, which,
preferably, should include the involvement of end-users. The process of designing screening
interventions for specific risk groups should involve discussions with those risk groups and
organizations that might work with these populations, especially groups that face specific
access barriers or discrimination. This should help in arriving at user-friendly, acceptable and
effective approaches and building demand for services and their use.

Those invited for screening should be provided with detailed information, including the
benefits and risks, and verbal informed consent should be obtained. The privacy and
confidentiality of all information related to screening should be ensured.

The risks of discrimination and stigmatization should be carefully assessed prior to initiating
screening. Depending on the risks identified for different target groups, measures may be
adapted to minimize the consequences. In particular, the legal status of migrants, both with
regards to their access to health services and the risk of expatriation if they are diagnosed
with TB, need to be fully considered when the screening approach is designed. Similarly,
when plans are made to screen specific occupational groups, it should be determined
whether workers have legal protection to ensure their right to care and to maintain
employment.

33
 2.5.3 Involving partner organizations and dividing roles

Many different partners can be involved in screening for TB, and it is preferable to integrate
TB screening into other screening and outreach activities to improve both the efficiency of
screening and the relevance for the users. Identifying appropriate entry points for screening
is critical, and this requires mapping the health-care providers and social-service providers
for relevant groups – for example, endocrinology departments caring for people with
diabetes or non-governmental organizations providing social support for vulnerable groups.
To offer screening in prisons, links must be established with correctional services, and,
likewise, screening in workplaces requires establishing dialogue with employers and
departments of occupational health.

The planning for and management of the required financial and human resources should
account for all possible stakeholders that may be involved. Similarly, planning should include
stakeholders who may be involved in developing supply chains for tests and equipment, as
well as referral chains to ensure that those who are screened receive appropriate care.
Good coordination between stakeholders is required in order to ensure complementary and
avoid overlap or that conflicting approaches being implemented.

It is not effective to implement TB screening unless treatment, care and support services are
of high quality. Implementing an effective systematic screening programme for TB provides
opportunities to enhance support for patients receiving treatment as part of the overall
outreach efforts, and this may improve not only detection but also treatment results.

If human resources are limited, those who are engaged to help in case-finding can and
should also support patients who are receiving TB treatment, especially patients who are
members of high-risk groups who may face more barriers to completing treatment.10 For
example, lay workers employed to screen people living with HIV can also provide treatment
support at the same facilities.

2.5.4 Mobilizing resources

Many times, national TB programmes will not have extra money in their core budgets to
carry out screening activities, and these funds will need to come from other sources.
However, once some screening activities have been shown to be effective, funding may be
made available from programme budgets for screening to form part of national TB
programmes’ activities (PLHIV, contact investigation).

As part of efforts to detect and treat all people with TB, screening activities need to be
prioritized in accordance with findings in the initial situation analysis. A national strategic
plan should be written to position for external funding for screening activities, and careful
planning and initial assessments should be readily available to support any planned
activities.

34
2.5.5 Pilot testing

It is critical to pilot test a newly designed screening programme to ensure that it operates as
designed. Piloting provides a valuable opportunity to test and refine new instruments,
protocols, data systems and management structures. It also allows for an initial evaluation
of the performance of the screening programme in terms of yield and costs to ensure that it
has the intended effects on case detection and to allow the design or the protocol to be
modified if necessary.

2.6 Monitoring, evaluating and modifying the programme

A monitoring and evaluation plan should be developed as part of any screening programme.
General conditions and risk-group-specific conditions for discontinuing screening should be
established from the outset – for example, in relation to yield, contribution to overall case
detection and improvement in treatment enrolment and outcomes, or cost per case
detected, or some combination of these.

Indicators need to be chosen and forms for collecting data need to be created for or
adapted to the specific objectives and local conditions. In order to monitor yield and the
NNS in each targeted risk group, an appropriate information system needs to be developed
to generate data about the number of people diagnosed with TB in relation to the number
of people approached, screened and tested. This information should be assessed
periodically, and the mix of approaches adjusted appropriately.

The general epidemiology of TB, the importance of different risk groups and the
epidemiology of TB within each group may change over time, and prioritization for
screening will have to be adapted accordingly.

Because some members of any particular risk population will eventually find their way to
diagnosis through the patient-initiated pathway if not screened, it is of interest to evaluate
what impact screening in a particular group has on overall additional notification in a larger
basic management unit or group of basic management units. This will require analysis of
notification trends, preferably with comparisons to control areas.

It is also important to measure whether screening activities are simply concentrating case-
finding in a few facilities, which may occur if a specific intervention is seen as beneficial and
information about it spreads through the community. This can result in increased
notification in one area and decreased notification in another.

Because one objective of screening is early detection, it may also be useful to measure
delays in diagnosis and treatment. This, however, will require special surveys.

35
 2.6.1 Developing a plan for monitoring and evaluation

Monitoring and evaluating systematic screening should be incorporated into the monitoring
and evaluation programmes used within the national TB programme. Targets should be set
for the expected yield, the NNS and costs in relation to benefits.

2.6.2 Proposed indicators

Approaches to screening will vary for different groups, and intervention-specific indicators
should be developed for each approach. In general, however, data on the indicators shown
in Figure 10 should be collected for each targeted risk group.

Figure 10. Data to be collected for most systematic screening programmes for tuberculosis
(TB)

From the data collected in Figure 10, the following basic indicators can be calculated for
each respective risk group:
x the proportion of people screened among those eligible (B/A);
x the proportion of people suspected of having TB among those screened (C/B);
x the proportion of people tested or evaluated for TB among patients suspected of
having TB (D/C);
x the proportion of people diagnosed among those screened (E/B) and tested (E/D);
x the proportion of people initiating treatment among those diagnosed (F/E);

36
 x the proportion of people successfully completing treatment among those who
initiated treatment (G/F).

It is critical to monitor the yield of bacteriologically confirmed TB versus bacteriologically

unconfirmed TB. A high proportion of TB cases that have not been confirmed with a
bacteriological test may indicate over-diagnosis and should lead to a closer evaluation of
screening and diagnostic routines.

Data may also be disaggregated by age and sex – but this requires that detailed data be
collected for each individual screened.

Additional indicators of process (such as the number of people reached and screened per
day, the time required for each step of the screening and diagnostic procedure, and the
number of people requiring referral) should be collected during the pilot phase of a
screening programme to ensure that it is operating as designed. However, once the
programme has been established, these additional indicators should be discarded and the
focus should be shifted to streamlining the programme and scaling it up.15

The uptake of screening in a risk group (that is, the proportion of those eligible for screening
who are actually screened) can be assessed only if the size of the target group has been well
defined. Normally, it is possible to obtain the relevant information for screening that is
conducted in health facilities, closed settings (such as prisons) and through contact
investigations. However, it is often difficult to obtain this information from outreach
screening programmes – for example, when screening is done in the community – although
the estimated population of a targeted community may be used to obtain a rough estimate
of the eligible population.

Whenever screening occurs, a baseline should be developed using historical data, if

available.31

2.6.3 Routines for recording and reporting

In order to obtain the information required for the indicators described above, a recording
and reporting system for TB screening needs to include:
x a log of the number of people screened in each risk group. A special register with
individual-level information for each person screened may be used to obtain more
refined data about subcategories of persons within a risk group. Collecting these data is
resource-intensive, but it may be relevant when a screening programme is started as
part of an operational research project. It may be feasible to collect this type of data on
a continual basis for certain risk groups, such as people seeking care in medical facilities;
x a register of all cases suspected of having TB who underwent further diagnostic
evaluation (if a register is used to collect individual-level information for all people who
are screened, then this information can be included in it);
x a column in the laboratory register for noting whether the tested patient was identified
through screening and to which risk group the patient belongs;

37
 x a column in the treatment register to note whether the patient was identified through
screening and to which risk group the patient belongs;
x other forms may be necessary depending on the approach used and the existing
registers. For example, if contact investigation will be implemented, there should be
specific forms to properly track this activity.

2.6.4 Programmatic evaluations

Based on the results from monitoring the indicators discussed above, a special assessment
may be needed to explore, for example, the reasons for a low uptake of screening, an
unexpectedly low proportion of people suspected of having TB identified by screening, a low
proportion of those suspected of having TB who had a diagnostic investigation, a higher
than expected NNS, or a high proportion of cases that are not bacteriologically confirmed.

Additional quantitative and qualitative analyses may be needed to determine whether there
are barriers to screening, to identify opportunities to improve the screening approach and
whether there have been any social consequences from the screening activities. It is also
prudent to evaluate the effects of screening on overall operations at health clinics,
especially the impact of an increased burden of laboratory testing.

2.6.5 Monitoring time trends for rescreening and reprioritization

A successful screening programme may lead to a diminishing yield over time, at least if the
risk group is a fixed population. Over time, changes in the background burden of TB as well
as changes in the profile of TB patients in the community (for example, a trend towards
fewer patients with symptomatic TB and fewer cases of smear-positive TB) can lead to a
reduction in the yield from screening, an increase in the NNS, a reduction in cost
effectiveness, and a change in the ratio of benefits to harms. Trends in all of these indicators
need to be monitored, and the prioritization of risk groups, choice of screening approach,
and screening interval should be reassessed regularly. Criteria for stopping screening should
be established before a screening initiative is implemented.

2.6.6 Research

Standard monitoring and evaluation procedures may be complemented by operational

research aimed at improving the performance of screening in the local setting as well as
research aimed at improving the global evidence base for screening. Research may aim at:
x assessing the accuracy and performance of different algorithms for screening and
diagnosis;
x identifying operational challenges and solutions;
x identifying the best ways to improve the acceptability of screening and minimize the
harms;
x establishing the effectiveness and cost effectiveness of screening in different risk groups
and in different epidemiological situations.

38
For a number of algorithms it may be useful to evaluate the PPV. Evaluating the PPV can be
much simpler than assessing accuracy, which includes evaluating the sensitivity of the
algorithm. Evaluating sensitivity requires testing a large number of persons with the
reference standard, but assessing the PPV requires only that those diagnosed as having TB
are tested with a reference standard.

In general there is a need for more, larger and better randomized trials to assess the short-
term and long-term effectiveness, and cost effectiveness of screening. Implementing such
studies requires careful planning and considerable resources.

39
 3. Web-based tool to assist risk group prioritization and
algorithm choices

3.1 Introduction to the tool

The most desirable screening strategy would be one with high total yield of true positive TB
cases, few false positives, low NNS, low cost, a rapid and simple algorithm, and high client
acceptability. In practice, many of these factors tend to run in opposite directions, so a
multifactorial analysis is needed.

An online tool has been developed to assist with the process of prioritizing risk groups for
screening and choosing appropriate screening and diagnostic algorithms. The tool allows
users to select one or a number of risk groups for exploration, and for each risk group
selected the tool estimates the yield and costs of screening and diagnosis for each different
screening algorithm.

The tool is intended as an aid to explore which risk groups that may potentially be screened
and which screening and diagnostic algorithms may be most appropriate to use. The tool
must not be used as the only source of information for prioritization, planning and
budgeting. Rather it can be used as a starting point for these processes, which are outlined
in section 2. The limitations of the tool are further discussed in section 3.3.

The online tool builds on a previous tool which was developed before the WHO issued
guidelines on systematic screening for active TB.32 The present tool models yields for the
screening algorithm options listed in the WHO guideline based on data from systematic
reviews of accuracy of different screening and diagnostic tests and assumed prevalence of
culture positive pulmonary TB among screened risk groups.33

All calculations are made for specific country settings. Some of the necessary information
(including TB prevalence in the general population and the sensitivity and specificity of
different screening and diagnostic tests) is prepopulated with estimates from various data
sources, while some information must be provided by the user. It is important to note that
much of the prepopulated generic data is based on point estimates from systematic reviews
(including studies up to 2012) and may not be applicable in a given setting. The accuracy of
diagnostic tests varies in certain groups and settings, and technologies are improving. The
user must therefore review all prepopulated estimates to ensure they are appropriate, and
make changes as required. The collection of relevant data to enter into the tool should be
part of the situation assessment (see section 2.1.3). Moreover, it is always advisable to
perform sensitivity analyses using confidence intervals or plausibility ranges for key
assumptions.

Users who are unfamiliar with interpretation of sensitivity, specificity and predictive values
of screening and diagnostic tests are advised to seek assistance from persons with expertise
in clinical epidemiology.

40
3.2. How to use the tool

The user begins by selecting the country for which screening will be modelled, and then
selects the risk groups to explore. The user then provides estimates, or confirms
prepopulated data, for the following inputs:

x Population size and TB prevalence of general population – The user can rely on
national estimates provided or can enter other estimates if better data is available or
for subnational calculations.

x Size of selected risk groups – This should be provided either as an absolute number
or as a proportion of the general population (equivalent to the prevalence of the risk
factor in the country).

x TB prevalence in selected risk groups – This should be provided either as an absolute

figure (per 100 000 population) or as the relative risk for TB in the group compared
with the risk in the general population. Relative risks for certain groups have been
provided based on data from systematic reviews; these estimates are prepopulated
in the tool. The user should review any prepopulated estimates to ensure they are
appropriate, and update as necessary with national estimates.

x Reachability and acceptability of screening – This is the proportion of each selected

risk group that may be reached by a screening programme, and then once reached,
the proportion of each selected risk group that may accept screening.

x Costs of screening and diagnostic tests – This is the estimated cost per screening or
diagnostic test performed in a screening programme. Estimates for the running costs
of test are provided for chest X-rays, sputum-smear microscopy and the Xpert
MTB/RIF assay, stratified by global region. The user should review test costs and add
start-up, operational and overhead costs.

The tool then generates the following estimates for each risk group selected:
x the number of people expected to be screened;
x the number of prevalent culture positive pulmonary TB cases;
x the number of true culture positive TB cases that may be detected, according to
the sensitivity of the screening algorithm used;
x the number of cases missed;
x the number of false-positive diagnoses expected, according to the specificity of the
screening algorithm used;
x the NNS to detect one true case of pulmonary TB; and
x the total cost and cost per true case detected for screening the selected risk group,
according to the screening algorithm used.

41
 To allow for easy visual comparison across risk groups and across screening algorithms, the
tool produces graphs of the potential yield of true-positive and false-positive cases (Figure
6), the NNS (Figure 7), the cost per case detected (Figure 8), and the costs versus yield
comparison of various potential screening algorithms (Figure 9).

In order to understand how variations in the estimated parameters and the targeted
populations affect estimates of size, yield and cost, the user should repeat the process of
generating estimates while varying some or all of the inputs and risk groups.

Figure 6. Potential yield of true-positive and false-positive cases of TB in three risk groups,
per screening algorithm used (Algorithms can be found in the annex)

42
Figure 7. The number needed to screen (NNS) to detect one true case of TB in three risk
groups with specified relative risks of TB, per screening algorithm used (Algorithms can be
found in the annex)

Figure 8. Screening and diagnostic costs per true case detected in three risk groups with
specified relative risks of TB, per screening algorithm used (Algorithms can be found in the
annex)

43
 Figure 9. Incremental costs and incremental yield of screening across screening algorithms
in two risk groups of specified size and TB prevalence, per screening algorithm used
(Algorithms can be found in the annex)

44
3.3 Limitations of the tool

There are several limitations to this tool that include but are not limited to the following:
x The estimates produced by the tool are based on a series of assumptions. Each
parameter entered into the tool is an estimate with inherent uncertainty. The
uncertainty across all of the parameters used in the tool compounds the overall
uncertainty of the estimates produced by the tool.

x The tool requires significant input from the user. Using the tool requires specific
inputs from the user, and some of these inputs can be difficult to estimate. The
resulting outputs from the tool are only as good as the data provided, both by the
tool and by the user.

x The tool does not account for overlaps among risk groups. It is likely that people
who belong to a risk group selected for targeted screening will also have other risk
factors and, therefore, will be part of one or several other risk groups. If a screening
programme includes many potentially overlapping risk groups, this overlap should be
adjusted for. It may also be prudent to consider and incorporate the potentially
increased risk for TB among people with many risk factors.

x The tool does not estimate the potential additional number of cases detected
through screening, nor the relative effectiveness compared with interventions to
improve the patient-initiated pathway. The estimated number of true cases that
can be detected through screening can not be assumed to be equal to additional
case detection since a proportion of them would be detected through health seeking.
The tool does not estimate additional case detection from efforts to improve the
patient-initiated pathway.

x The tool does not model the impact of screening on the future prevalence or
incidence of TB. Estimates are cross-sectional and do not incorporate any future
changes in the epidemiology of TB. When screening is repeated in the same
population at regular intervals, the prevalence and incidence of TB may diminish,
especially in confined populations, such as in prisons. The tool only estimates the
yield of the first screening round. For subsequent screening rounds the user will have
to adjust inputs in line with assumed change in TB prevalence. The tool cannot be
used to predict impact on TB transmission and long term effects on TB incidence. For
this, dynamic transmission modelling is required.

x The tool does not estimate impact on diagnostic delay, disease severity at time of
diagnosis, or improvement in treatment outcomes from early treatment initiation.

x The tool does not incorporate elements of equity and fairness.

For these reasons the tool is meant to serve only as an aid in the process of prioritizing risk
groups for screening and choosing screening algorithms. It should not be used for detailed
planning, or for projection of future impact on TB epidemiology. See section 2 for other
elements of the planning and implementation process.

45
 References
1. World Health Organization. Global Tuberculosis Report, 2013. Geneva: World Health
Organization, 2013.
2. Storla DG, Yimer S, Bjune GA. A systematic review of delay in the diagnosis and
treatment of tuberculosis. BMC public health 2008; 8: 15.
3. Raviglione M, Marais B, Floyd K, et al. Scaling up interventions to achieve global
tuberculosis control: progress and new developments. Lancet 2012; 379(9829): 1902-13.
4. World Health Organization. Global strategy and targets for tuberculosis prevention,
care and control after 2015: Post-2015 global tuberculosis strategy framework. Geneva:
World Health Organization, 2014.
5. Uplekar M, Weil D, Lonnroth K, et al. WHO's new End TB Strategy. Lancet 2015.
6. World Health Organization. Systematic screening for active tuberculosis: Principles
and recommendations. Geneva: World Health Organization, 2013.
7. Raviglione MC, Uplekar MW. WHO's new Stop TB Strategy. Lancet 2006; 367(9514):
952-5.
8. World Health Organization. An expanded DOTS framework for effective tuberculosis
control. Geneva: World Health Organization, 2002.
9. Corbett EL, MacPherson P. Tuberculosis screening in high human immunodeficiency
virus prevalence settings: turning promise into reality. The international journal of
tuberculosis and lung disease : the official journal of the International Union against
Tuberculosis and Lung Disease 2013; 17(9): 1125-38.
10. Golub JE, Dowdy DW. Screening for active tuberculosis: methodological challenges in
implementation and evaluation. The international journal of tuberculosis and lung disease :
the official journal of the International Union against Tuberculosis and Lung Disease 2013;
17(7): 856-65.
11. Kranzer K, Afnan-Holmes H, Tomlin K, et al. The benefits to communities and
individuals of screening for active tuberculosis disease: a systematic review. The
international journal of tuberculosis and lung disease : the official journal of the
International Union against Tuberculosis and Lung Disease 2013; 17(4): 432-46.
12. Lönnroth K, Corbett E, Golub J, et al. Systematic screening for active tuberculosis:
rationale, definitions and key considerations. The international journal of tuberculosis and
lung disease : the official journal of the International Union against Tuberculosis and Lung
Disease 2013; 17(3): 289-98.
13. Uplekar M, Creswell J, Ottmani SE, Weil D, Sahu S, Lönnroth K. Programmatic
approaches to screening for active tuberculosis. The international journal of tuberculosis
and lung disease : the official journal of the International Union against Tuberculosis and
Lung Disease 2013; 17(10): 1248-56.
14. Zenner D, Southern J, van Hest R, et al. Active case finding for tuberculosis among
high-risk groups in low-incidence countries. The international journal of tuberculosis and
lung disease : the official journal of the International Union against Tuberculosis and Lung
Disease 2013; 17(5): 573-82.
15. World Health Organization. Recommendations for investigating contacts of persons
with infectious tuberculosis in low- and middle-income countries. Geneva, 2012.
WHO/HTM/TB/2012.9.
16. World Health Organization. Early detection of tuberculosis: An overview of
approaches, guidelines, and tools. Geneva, 2011. WHO/HTM/STB/PSI/2011.21.

46
17. World Health Organization. Engaging all health care providers in TB control:
Guidance on implementing public-private mix approaches. Geneva: World Health
Organization, 2006.
18. World Health Organization. Practical approach to lung health (PAL): A primary health
care strategy for integrated management of respiratory conditions in people of five years of
age and over. Geneva: World Health Organization, 2005.
19. World Health Organization. Improving the diagnosis and treatment of smear-
negative pulmonary and extrapulmonary tuberculosis among adults and adolescents:
Recommendations for HIV-prevalent and resource-constrained settings. Geneva, 2007.
WHO/HTM/TB/2007.379 & WHO/HIV/2007.1
20. World Health Organization. Rapid implementation of the Xpert MTB/RIF diagnostic
test: Technical and operational “how-to‟: Practical considerations. Geneva: World Health
Organization, 2011. WHO/HTM/TB/2011.2.
21. World Health Organization. Tuberculosis prevalence surveys: a handbook. Geneva:
World Health Organization, 2011.
22. World Health Organization. Understanding and using tuberculosis data. Geneva:
World Health Organization, 2014.
23. World Health Organization. Framework for conducting reviews of tuberculosis
programmes. Geneva: World Health Organization, 2014.
24. World Health Organization. Public–Private Mix for TB Care and Control: A tool for
national situation assessment. Geneva: World Health Organization, 2007.
25. World Health Organization. ENGAGE-TB: integrating community-based tuberculosis
activities into the work of nongovernmental and other civil society organizations. Geneva:
World Health Organization, 2012.
26. Tuberculosis Coalition for Technical Assistance. The Tool to Estimate Patients’ Costs
2008.
27. Contributing to health system strengthening - Guiding principles for national
tuberculosis programmes. WHO/HTM/TB/2008.400. Geneva: World Health Organization,
2008.
28. World Health Organization. Guidelines on the management of latent tuberculosis
infection. Geneva: World Health Organization, 2015.
29. World Health Organization. Guidelines for the programmatic management of drug-
resistant tuberculosis – 2011 update. Geneva: World Health Organization, 2011.
30. World Health Organization. Guidelines for intensified tuberculosis case-finding and
isoniazid preventive therapy for people living with HIV in resource-constrained settings.
Geneva: World Health Organization, 2010.
31. Blok L, Creswell J, Stevens R, et al. A pragmatic approach to measuring, monitoring
and evaluating interventions for improved tuberculosis case detection. International health
2014; 6(3): 181-8.
32. Nishikiori N, Van Weezenbeek C. Target prioritization and strategy selection for
active case-finding of pulmonary tuberculosis: a tool to support country-level project
planning. BMC Public Health 2013 Feb 2;13:97
33. van ’t Hoog AH, Onozaki I, Lönnroth K. Choosing algorithms for TB screening: a
modelling study to compare yield, predictive value and diagnostic burden. BMC Infectious
Diseases 2014; 14: 532. doi: 10.1186/1471-2334-14-532.

47
 Annex 1. Ten potential screening and diagnostic algorithms.

48
49
50
51
52
53
54
55
56
57
58