Chapter 14 of the Canadian Tuberculosis Standards: Prevention and control of tuberculosis transmission in healthcare settings

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Authors and affiliations

B. Lynn Johnston; Division of Infectious Diseases, Department of Medicine, Dalhousie University, Nova Scotia Health Authority, Halifax, Nova Scotia, Canada

Toju Ogunremi; Centre for Communicable Diseases and Infection Control, Public Health Agency of Canada, Ottawa, Ontario, Canada

Katherine Defalco; Centre for Communicable Diseases and Infection Control, Public Health Agency of Canada, Ottawa, Ontario, Canada

Noémie Savard; Secteur Prévention et contrôle des maladies infectieuses, Direction régionale de santé publique, Centre intégré universitaire de santé et de services sociaux du Centre-Sud-de-l'île-de-Montréal, Montréal, Québec, Canada

Stephanie W. Smith; Division of Infectious Diseases, Department of Medicine, University of Alberta, University of Alberta Hospital, Edmonton, Alberta, Canada

Key points

1. Introduction and general principles

While the overall incidence of tuberculosis (TB) in Canada is low, it is higher in certain population groups and geographic regions and exposure to people with unsuspected respiratory TB, whether patients, visitors or other health care workers (HCWs), followed by its transmission, does occur in healthcare settings. As detailed in Chapter 1: Epidemiology of tuberculosis in Canada, populations at higher risk of active TB include Indigenous Peoples, those born or previously residing in high-TB-incidence countries (especially low- and high-human immunodeficiency virus (HIV) prevalence regions in Africa, and the Western Pacific and Southeast Asia regions), HIV-infected persons and people with a history of active TB disease. Staff and residents of homeless shelters and injection drug users may have a higher risk of TB than the general population.Footnote 1Footnote 2

While some studies have indicated that HCWs are at increased risk of occupationally acquired TB,Footnote 3 more recent literature from a number of low-TB-incidence countries has found that the rate of latent and active TB infection in HCWs is similar to that in the general population, particularly after adjusting for country of birth.Footnote 4Footnote 5Footnote 6Footnote 7Footnote 8Footnote 9Footnote 10 However, occupationally acquired TB does occur.Footnote 11Footnote 12Footnote 13Footnote 14Footnote 15 Occupational risk factors appear to be providing direct care to those with respiratory TB and participation in aerosol-generating medical procedures on individuals with infectious TB.Footnote 16Footnote 17Footnote 18

In hospitals and other settings where people congregate and share indoor air (in the same room or via the building ventilation system), the risk of M. tuberculosis transmission can be increased if ventilation and other infection prevention and control (IPC) measures are inadequate.Footnote 11Footnote 12Footnote 16Footnote 19 A number of studies have identified that TB exposures within healthcare facilities are most often due to failure to suspect or diagnose active TB and implement appropriate IPC measures.Footnote 12Footnote 16Footnote 17Footnote 20Footnote 21Footnote 22Footnote 23Footnote 24 As a result, recommendations for the prevention of healthcare-associated transmission of M. tuberculosis to HCWs, patients/residents and visitors have been developed.Footnote 25Footnote 26Footnote 27 Despite limited high-quality evidence on preventing TB transmission, implementation of the recommended hierarchy of IPC measures in hospitals in high-income countries was followed by a reduction in its transmission.Footnote 28

This chapter reviews factors that determine or affect transmission of M. tuberculosis within hospitals and other healthcare settings, while focusing on measures to prevent transmission.

Recommendations provided are based, as much as possible, on published evidence. Evidence from randomized controlled trials, generally considered the strongest level of evidence, is limited, as this is generally not feasible when analyzing risk factors or situations involving natural exposure (e.g., TB outbreaks). As a result, all available evidence comes from observational studies, such as cohort studies and outbreak investigations. This chapter cites the evidence base from these primary studies, published literature reviews and a grey literature search of relevant international guidelines.Footnote 25Footnote 27Footnote 29Footnote 30Footnote 31Footnote 32

1.1. Determinants of transmission in healthcare settings

Aerosolization of infectious M. tuberculosis bacteria occurs when individuals with respiratory TB cough, sneeze, sing, or speak. Aerosol-generating medical procedures (e.g., bronchoscopy, intubation, sputum induction), and some patient-care activities (e.g., irrigating a mycobacterial-containing wound), laboratory and autopsy procedures can also cause aerosolization of mycobacteria. Once infectious M. tuberculosis bacteria are aerosolized, they may be carried throughout a room or building by air currents and inhaled by another individual, with the possibility of TB infection. Although the risk of transmitting M. tuberculosis is highly variable, the presence of certain factors (discussed in the following sections) predicts an increased transmission risk. In general, the more of these factors present, the greater the risk of M. tuberculosis transmission (see Chapter 2: Transmission and pathogenesis of tuberculosis).

1.2. Factors associated with increased risk of health care-associated M. tuberculosis

1.2.1. Delayed diagnosis

Many outbreak investigations, as well as a root-cause analysis exploring factors contributing to TB exposures in a tertiary-care hospital in Canada, identify delay in making the diagnosis of TB as the most common reason for the exposures (see Appendix 1 and Appendix 2, Table 2c).Footnote 11Footnote 12Footnote 16Footnote 17Footnote 18Footnote 20Footnote 21Footnote 22Footnote 23Footnote 33Footnote 34Footnote 35Footnote 36Footnote 37Footnote 38Footnote 39Footnote 40Footnote 41 The root-cause analysis noted failures to consider TB as a possible diagnosis and failure to obtain or correctly interpret imaging findings as common errors, with 80% of the errors being preventable.Footnote 20 A Canadian study examining IPC failures contributing to bronchoscopy-associated exposures found a failure to obtain a pre-procedure sputum or determine whether the patient was known to have a positive sputum smear prior to the procedure.Footnote 42 Even when TB has been initially considered in the diagnosis, precautions may be inappropriately discontinued if HCWs have not been systematic in determining whether the diagnosis has been accurately excluded. The importance of considering a diagnosis of TB, and not prematurely excluding it, in an individual presenting with sub-acute or chronic respiratory symptoms, even when an alternate diagnosis is plausible, cannot be over-emphasized.

1.2.2. Number of patients with respiratory TB

It seems intuitive that a larger number of hospitalized patients with respiratory TB is an important determinant of higher institutional transmission risk. However, results from a study involving 17 acute care hospitals in Canada showed that institutional risk of M. tuberculosis transmission was better correlated with delayed diagnosis and treatment which in turn was associated with having a small number of admissions with respiratory TB disease.Footnote 43 The study results suggest that healthcare facilities with more experience managing patients with TB are, not surprisingly, less likely to miss a diagnosis of respiratory TB and that facilities seeing fewer patients with TB need ongoing reeducation on recognizing a patient who might have respiratory TB.

1.2.3. Inadequate ventilation

The exchange of indoor air with outdoor air reduces the risk of infection transmission by diluting the concentration of viable airborne M. tuberculosis bacteria present. Several studies report inadequate ventilation as a risk factor that contributes to transmission.Footnote 11Footnote 22Footnote 23Footnote 44

1.2.4. Duration of exposure and proximity to infectious patient

The risk of TB infection varies with duration of exposure, form of tuberculous disease, and type of patient care activity. Even when the relative risk of infection is low, close proximity and repeated exposure can lead to a higher cumulative risk.Footnote 24Footnote 34

1.3. Risk classification

1.3.1. Healthcare settings

The risk of healthcare-associated transmission of M. tuberculosis to HCWs, patients/residents and visitors varies with the type of setting, occupational group, effectiveness of TB IPC measures and patient/resident population. Previous Canadian guidance provided thresholds for annual numbers of patients admitted with respiratory TB that could be used by facilities to determine their risk for healthcare-associated transmission of TB and guide their IPC interventions. Given the annual number of TB cases alone may not accurately reflect risk and that other factors such as effectiveness of IPC measures must be taken into account,Footnote 43 this type of risk classification may no longer be suitable. A review of the community profile of TB disease and the number of TB admissions in the course of a year, independent of a risk-classification scheme, should inform determination of a healthcare facility and unit risk category as a framework to predict whether and where their HCWs are at increased risk of TB exposure and guide their IPC strategies.

1.3.2. Health care worker activities

Patient-care activities are associated with varying degrees of exposure risk and subsequent infection with M. tuberculosis. Performing high-risk procedures and activities are contributing factors to transmission of M. tuberculosis.Footnote 16 The risk of transmission increases with the duration of exposure and higher amounts of airborne mycobacteria. As a result, it is recommended that HCWs perform a risk assessment prior to interactions with all patients, including people with confirmed TB or who have symptoms of TB.Footnote 45 This risk assessment involves evaluating the likelihood of exposure to M. tuberculosis for a specific patient-care activity, with a specific patient, in a specific environment and under particular conditions. This is referred to as a point-of-care risk assessment and is described in the Public Health Agency of Canada's (PHAC's) Routine Practices and Additional Precautions for Preventing the Transmission of Infection in Healthcare Settings.Footnote 45 The point-of-care risk assessment informs HCWs' decisions regarding the IPC measures needed to minimize the risk of exposure for themselves, other HCWs, patients and visitors.

1.3.2.1. High-risk activities
1.3.2.2. Intermediate-risk activities
1.3.2.3. Low-risk activities

Risk can be mitigated by use of engineering and administrative controls and appropriate personal protective equipment (PPE).

2. Prevention and control of transmission of M. tuberculosis in healthcare settings

Recommendations for the prevention of healthcare-associated transmission of M. tuberculosis involve application of a tiered framework of measures that enables healthcare organizations to comprehensively evaluate the risk of HCW exposure to workplace hazards, including M. tuberculosis, and the effectiveness of the organization's mitigation responses.Footnote 45 This involves collaboration between IPC, Occupational Health Safety and Wellness and building engineers.

The ideal approach to containing a hazard is to implement a hierarchy of controls: 1) elimination; 2) substitution; 3) engineering controls; 4) administrative controls; and 5) PPE.Footnote 46 Elimination of TB from the healthcare setting is not always possible, but effective treatment of respiratory TB is equivalent. Substitution is not a relevant approach to preventing transmission of TB.

3. Engineering controls

These are measures built into healthcare facility design to reduce the likelihood of HCW, patient/resident and visitor exposure to viable airborne M. tuberculosis. They reduce the number of infectious particles in the air by ventilation, high-efficiency particulate air (HEPA) filtration and/or disinfection using ultraviolet germicidal irradiation (UVGI). It is important that engineering controls be regularly checked to ensure that they meet recommendations.Footnote 27

3.1. Ventilation

The exchange of indoor air with outdoor air reduces the risk of infection by diluting the concentration of airborne pathogens. Theoretically, the risk of transmission should decrease with increasing fresh-air ventilation.

To achieve a balanced ventilation system, the amount of supply air (air mechanically pushed into a room) and the amount of exhaust air (air mechanically pulled from a room) must be set to ensure room conditions are stable. Factors such as infiltration (e.g., space around doors, windows and curtains), doors and conditions of an adjacent room need to be considered when balancing a ventilation system.

Ventilation recommendations for airborne infection isolation rooms and other select areas are of critical importance because of their positive impact on reducing the risk for healthcare-associated transmission of M. tuberculosis. The supply and exhaust air system need to be properly designed to achieve effective air changes within a space. The location of the supply and exhaust air diffusers, the speed of the air, furniture in the room and other items that affect air flow patterns will affect the effectiveness of the air changes per hour (ACH). Increasing the number of ACH from 1 to 6 will result in more rapid clearing of infectious airborne microorganisms from the room air. However, further increases above 6 ACH will have progressively less effect, and increases above 12 ACH may provide minimal additional benefit.Footnote 47Footnote 48 In general, as ACH rates are increased, there are increased costs for building and maintaining the ventilation system. Pressurization, which prevents particulates from leaving the room through infiltration, is equally, if not more, important than ACH. Pressurization is also critical for when doors are opened and closed, to ensure that air keeps flowing into the room and not out through the door. Opening the window may cause reversal of the direction of air flow, depending upon the prevailing wind direction and outdoor temperature.

A number of organizations and agencies, such as American Society of Heating, Refrigerating and Air-Conditioning Engineers (ASHRAE), Canadian Standards Association (CSA) and Centers for Disease Control and Prevention (CDC) have published recommendations regarding ventilation levels to reduce the risk of healthcare-associated transmission of airborne pathogens, such as M. tuberculosis.Footnote 49Footnote 50Footnote 51 Differences among their recommendations (Table 1) are not based on differing evidence but, rather, on the risk-benefit assessment of each organization. In deciding which recommendations to implement, hospital administrators may take into account factors such as facility design, latest scientific evidence, facility risk assessment, financial resources, environmental conditions and, at a minimum, provincial and territorial building regulations.

Table 1. Ventilation recommendations for selected areas in healthcare facilities
Area/function Minimum total ACHFootnote a Relative pressurizationFootnote b
(CSA 2019)
ExhaustFootnote bFootnote c
(CSA 2019)
CDC 2019Footnote 49 CSA 2019Footnote 50 ASHRAE 2021Footnote 51
AIIR 12 12 12 Negative DedicatedFootnote d
Ambulatory care clinic NA 9 4 NegativeFootnote e DedicatedFootnote d
Autopsy (general zone) 12 20 12 NegativeFootnote e DedicatedFootnote d
Bronchoscopy 12 20 12 Negative RequiredFootnote f
ED waiting rooms 12 12 12 Negative DedicatedFootnote d
ED trauma room, life support 15 15 15 Positive NR
General diagnostic imaging suites (includes CT, MRI, X-ray, ultrasound) 6Footnote g 9 6 Equal NR
Microbiology laboratoryFootnote h 6 NA 6 NA NA
Operating rooms 15 20 20 Positive NR
Anteroom for operating rooms used for patients with airborne infection NA 9Footnote i NA Negative to operating rooms and contiguous spaceFootnote j Air removed from anteroom and from the operating rooms shall be exhausted to the outdoors
Patient room in an acute care facility 6 4-6 4Footnote k Equal NR
Resident room in a LTCH 2 4 2 Equal NR
Resident gathering areas in a LTCH 4 NA 4 NA NR
Sputum induction/ pentamidine aerosol administration NA NA 12 NA LocalFootnote l

Notes:
This table provides key information related to ventilation and does not replace information found in the relevant standards and guidelines. For further details, consult the complete guidelines and/or standards. Adapted from tables in the CDC,Footnote 49 CSAFootnote 50 and ASHRAEFootnote 51 documents.

Abbreviations:
ACH, air changes per hour; CDC, Centers for Disease Control and Prevention; CSA, Canadian Standards Association; ASHRAE, American Society of Heating, Refrigerating and Air-Conditioning Engineers; AIIR, airborne infection isolation room; NA, not addressed; ED, emergency department; NR, no requirement; CT, computed tomography; MRI, magnetic resonance imaging; LTCH, long-term care home; HVAC, heating, ventilation, and air conditioning; HEPA, high-efficiency particulate air.

Footnotes:

Footnote a

As per CSA, "minimum air change rate can be defined by either the supply or the exhaust depending on the situation. If defined by the exhaust flow rate, supply shall be chosen/configured to ensure consistent air quality and to meet heating and cooling needs. In all cases, the minimum outdoor air change rate shall be maintained."Footnote 50

Return to footnote a referrer

Footnote b

Recommendations from CSA (2019)Footnote 50 only. See full versions of ASHRAE (2021)Footnote 51 standard or CDC (2019)Footnote 49 guideline for further detail on relative pressurization (or pressure relationship) and exhaust (or direction of air movement).

Return to footnote b referrer

Footnote c

Clinics/facilities that have rooms where airborne disease is of concern and/or aerosol-producing medical procedures are performed should have ventilation for negative directional airflow for airborne disease prevention (e.g., dedicated exhaust or HEPA-filtered exhaust).Footnote 50

Return to footnote c referrer

Footnote d

An exhaust system that extracts air from spaces or through equipment of similar function that cannot be recirculated or transferred.Footnote 50

Return to footnote d referrer

Footnote e

For patient care areas or an area that is intended for the provision of services that directly supports patient care areas.Footnote 50

Return to footnote e referrer

Footnote f

High-level air separation requirements shall apply.Footnote 50

Return to footnote f referrer

Footnote g

X-ray (diagnostic and treatment).Footnote 49

Return to footnote g referrer

Footnote h

The Canadian Biosafety Standard (Second Edition 2015) describes the HVAC requirements associated with specific laboratory activities (i.e., diagnostic or research).Footnote 52

Return to footnote h referrer

Footnote i

Value extrapolated from "Anterooms for special precautions rooms".Footnote 50

Return to footnote i referrer

Footnote j

As per CSA, anterooms shall be provided for operating rooms used for patients with airborne infectious disease (e.g., TB). The anteroom pressure shall be maintained negative to both the operating room and the contiguous space; air shall flow from the operating room into the anteroom and from the corridor into the anteroom.Footnote 50

Return to footnote j referrer

Footnote k

For single-bed patient rooms using Group D diffusers, a minimum of 6 total ACH shall be provided and calculated based on the volume from finished floor to 6 feet (1.83 metres) above the floor.Footnote 51

Return to footnote k referrer

Footnote l

Rooms or booths used for these procedures shall be provided with local exhaust ventilation designed to capture contaminants as close to the source of emission as possible.Footnote 50

Return to footnote l referrer

3.1.1. General hospital areas

Adequate ventilation in general areas such as inpatient, examination and treatment rooms is important because people with unsuspected respiratory TB may be placed in them, posing a risk of transmission to other patients and HCWs.Footnote 44Footnote 53 Ventilation in these areas may be poor and further disrupted by opening and closing doors, installation of ceiling fans post-design and use of items such as ground circulation fans and electric heaters.

3.1.2. Airborne infection isolation rooms

Measures to ensure that adequate ventilation is in place for airborne infection isolation rooms are outlined in the following sections and discussed in more detail in other guidelines.Footnote 45Footnote 54

Regulation:

Good practice statements:

3.1.3. Sputum induction and administration of aerosolized pentamidine

The smaller the room where these procedures are performed, the easier and more practical it is to achieve required ventilation levels. Sputum collection booths, which are a type of enclosed local exhaust ventilation device, are commercially available for these purposes.

Good practice statements:

3.1.4. Bronchoscopy and autopsy

Areas where these procedures are performed tend to be much larger than inpatient rooms, making it difficult to achieve consistently high levels of ventilation with an inward direction of air flow.

Good practice statement:

3.1.5. Entering a room after generation of infectious aerosols has ended or patient with respiratory TB has been discharged

Table 2 provides guidance on when it is safe to enter a room previously occupied by a patient with respiratory TB without needing to wear a respirator or when a procedure room can be used for another patient after generation of infectious aerosols has ceased. The time required to remove airborne particles from an enclosed space depends on the number of ACH, which is a function of the volume (cubic feet of air) in the room or booth; the rate at which air is exiting the room or booth; the location of the ventilation inlet and outlet; and the configuration of the room or booth.Footnote 49 The minutes required to allow at least 99% removal of airborne microorganisms is considered sufficient to allow room entry.

Table 2. Time needed (by number of air changes per hour) to remove airborne microorganisms after generation of infectious droplet nuclei has ceasedFootnote a
Air changes per hour Minutes required for removal of airborne microorganisms
99% removal 99.9% removal
2 138 207
4 69 104
6 46 69
12 23 35
15 18 28
20 14 21

Footnotes:

Footnote a

This table was adapted from the CDC recommendations.Footnote 25

Return to footnote a referrer

3.2. Filtration

HEPA filters have a minimum removal efficiency of 99.97% for all particles.Footnote 30Footnote 49 Air can be recirculated through HEPA filters in areas in which no general ventilation system is present, an existing system is incapable of providing sufficient ACH or air-cleaning (particulate removal) without affecting the fresh air supply or negative-pressure system is desired.Footnote 30Footnote 49

Small HEPA units, either fixed or portable, may be used to filter recirculated air in a room. Portable industrial grade HEPA units, sometimes referred to as Room Air Purifiers with a HEPA filter, are available that can filter air at a range of airflows. The quality of these units must be carefully analyzed by the hospital engineering department prior to purchase and use. Placement of the unit within the room must be specified by this department to ensure laminar airflow distribution and maximize air changes throughout the room. HEPA filters must be installed to ensure that air flowing through the unit cannot bypass the filter. Refer to the CDC guideline for additional details.Footnote 49

HEPA filters typically last 5-10 years if a proper pre-filter to protect it from common environmental particles is used and maintained. HEPA filters require regular monitoring to ensure that the filter has not clogged, which will result in decreased filtering efficiency. For further information on HEPA filtration and details on safety issues when handling spent filters, refer to the CDC guidelines.Footnote 49

Good practice statements:

3.3. Ultraviolet germicidal irradiation

Ultraviolet germicidal irradiation (UVGI) is effective at inactivating airborne bacteria and in reducing the risk of M. tuberculosis transmission.Footnote 55Footnote 56Footnote 57 Upper-room UVGI directs UV-C energy to the upper portions of a room to create a disinfection zone so that pathogens in the air that pass through this disinfection zone are inactivated.Footnote 58 The effectiveness of upper-room UVGI depends on multiple factors, including UVGI dose, air circulation, ventilation, temperature, humidity, room configuration and proper UVGI system installation and maintenance.

The interest in UVGI in IPC is growing, and safety and application standards are in development. However, safety data, real-world effectiveness and accepted industry standards remain limited. For further information on UVGI, refer to the CDC environmental guidance document.Footnote 49

3.4. Equipment cleaning and disinfection

As transmission of M. tuberculosis in healthcare settings occurs almost exclusively by the airborne route, preventive measures target airflow controls and ventilation systems. However, there have been rare instances of transmission via improperly reprocessed bronchoscopes.Footnote 59Footnote 60

Good practice statement:

4. Administrative controls

These are institutional policies or measures that 1) aim to reduce the time between the arrival of an individual with undiagnosed respiratory TB at a healthcare facility and making a presumptive diagnosis of their condition, placing the patient on airborne precautions, establishing the diagnosis and starting antimicrobial treatment; 2) provide the HCW with respiratory protection; and 3) evaluate the effectiveness of its IPC strategies and interventions.

4.1. TB infection prevention and control program

The goal of a TB IPC Program is to prevent M. tuberculosis transmission to HCWs, patients/residents/clients and visitors.

Good practice statements:

4.1.1. Risk assessment

The first step of an effective TB IPC Program in every healthcare setting should be to perform an organizational risk assessment in order to understand what measures are required to decrease the risk of patient/resident/client, visitor and HCW exposure to M. tuberculosis. The exposure risk for HCWs engaged in different activities should be evaluated during this assessment. For further information on an organizational risk assessment, refer to PHAC's Routine Practices and Additional Precautions for Preventing the Transmission of Infection in Healthcare Settings.Footnote 45

Good practice statements:

4.1.2. Respiratory protection program

Essential components of a respiratory protection program are selecting appropriate respirators (N95 or equivalent) for HCWs and HCW education regarding the occupational risk of TB, the role of respiratory protection in reducing that risk and the correct use of respirators, including performing a seal check.Footnote 61 For cost-efficiency purposes, it is important to provide respirator models with inherently good fit characteristics that will fit the majority of HCWs.

4.1.2.1. Respirators

Respiratory protection of HCWs involves the use of a Health Canada-approved respirator with a filter class equivalent to or higher than an N95, to prevent inhalation of aerosols containing infectious microorganisms.Footnote 45 These respirators are certified to filter 95% of particles of diameter 0.3 microns (µm) or larger with less than a 10% leak, thus protecting wearers against airborne infectious microorganisms such as M. tuberculosis.Footnote 25 Medical masks are not designed for respiratory protection of HCWs against M. tuberculosis.

4.1.2.2. Fit testing

Fit testing is used to determine whether a particular size and model of respirator fits a given person, by assessing leakage around the face-respirator seal. Each time the HCW puts on a respirator, a user seal check (according to manufacturer's instructions) is required to determine whether the respirator is properly sealed to the face. Most Canadian jurisdictions require fit testing for HCWs to determine their ability to obtain a satisfactory seal during respirator use.Footnote 62 HCWs are referred to jurisdictional requirements regarding the processes and frequency of fit testing. In the absence of requirements, consult provincial/territorial public health authorities.

Regulations:

Good practice statements:

4.1.3. Identifying individuals with respiratory TB in the healthcare setting

Healthcare-associated transmission of TB to other patients and HCWs is uncommon; when it occurs, however, it is most often due to a failure to consider respiratory TB in the diagnosis and to place the patient/resident on airborne precautions.Footnote 11Footnote 14Footnote 20Footnote 24 One factor leading to delayed diagnosis is not realizing that the patient (or family member) is at risk for TB.Footnote 22 This may be especially relevant in the patient with minimal respiratory symptoms who is presenting for unrelated reasons, including labour and delivery.Footnote 63Footnote 64 For young children (less than five years old) with respiratory TB, it should be noted that they likely recently acquired their infection from an adult family member with active respiratory TB, who may pose a risk to HCWs and other patients while visiting the child in hospital.Footnote 63Footnote 65

Even when the diagnosis of respiratory TB is considered, it may be discounted in the patient for whom another diagnosis seems plausible, such as a non-mycobacterial, community-acquired pneumonia, lung abscess or malignancy, and airborne precautions prematurely discontinued (see Appendix 2, Table 2d). Guidelines that direct HCWs on when to consider the diagnosis of respiratory TBFootnote 66Footnote 67Footnote 68 and place the patient on airborne precautions, and under what circumstances airborne precautions can be discontinued, as well as regular HCW education on those guidelines, are important administrative controls.

The diagnosis of TB rests on detection of M. tuberculosis from a respiratory tract specimen.Footnote 69Footnote 70 Three sputum specimens (spontaneous, induced or post-bronchoscopy) from adolescents and adults can be collected on the same day, a minimum of one hour apart. Three gastric washes can be collected from young children in the same morning. A single negative smear from bronchial alveolar lavage does not definitively exclude respiratory TB disease but may be used in certain situations where it is not possible to collect sputum (see Chapter 3: Diagnosis of tuberculosis disease and drug-resistant tuberculosis).

Good practice statements:

4.1.4. Airborne precautions

Airborne precautions refer to multiple measures applied to prevent airborne exposure to M. tuberculosis in the healthcare setting (see Figure 1). They include source-control measures, patient accommodation, limiting patient movement and use of respirators, all to reduce the risk of patient-to-patient and patient-to-HCW transmission.

In Figure 1, the image and text description footnotes refer to the following:

  1. see section 4.1.3. Identifying individuals with respiratory TB in the healthcare settings
  2. see section 4.1.4. Airborne precautions
  3. see Chapter 3: Diagnosis of tuberculosis disease and drug-resistant tuberculosis
  4. see Chapter 5: Treatment of tuberculosis disease

The abbreviations are as follows:

Figure 1. Isolation of patients with, or being evaluated for, respiratory tuberculosis (TB) in healthcare settings
Figure 1
Figure 1: Text description

An algorithm for the assessment of patients presenting to a healthcare setting with, or being evaluated for, respiratory TB is a tool to guide isolation requirements.

  • The algorithm begins with a patient with or being evaluated for respiratory TB being identified in the healthcare setting. For additional information on identifying individuals with respiratory TB in the healthcare setting, refer to section 4.1.3.
  • When the patient with or being evaluated for respiratory TB is identified in the healthcare setting, airborne precautions should be initiated. Refer to section 4.1.4 for further information on airborne precautions. At this point, IPC personnel should be advised if the patient is admitted to hospital. If there is limited availability of airborne infection isolation rooms, priority for patient placement should be determined by a risk assessment. Further information on risk assessment is available in section 4.1.4.
  • Following this, the patient should undergo microbiological investigations to confirm respiratory TB, guided by recommendations in Chapter 3: Diagnosis of Tuberculosis Disease and Drug-resistant Tuberculosis. It should then be determined if respiratory TB has been confirmed in this patient, following recommendations outlined in Chapter 3: Diagnosis of Tuberculosis Disease and Drug-resistant Tuberculosis. If yes, then the patient should be reported to public health authorities. While the patient remains in hospital, airborne precautions should be maintained until the patient is no longer infectious, as defined in Chapter 5: Treatment of Tuberculosis Disease.
  • If respiratory TB is not confirmed, the patient should be assessed to determine if there is an alternate diagnosis and if concomitant respiratory TB has been excluded, as per section 4.1.4. If no to either of these, the healthcare provider should continue microbiological investigations to confirm respiratory TB. If yes to both of these, airborne precautions can be discontinued. For more information on the discontinuation of airborne precautions, refer to section 4.1.4.

Medical masks include procedure masks and surgical masks. Either type of medical mask, when worn by patients with respiratory TB, serves as a source-control measure to trap infectious respiratory secretions and is not intended as a form of PPE for the wearer.Footnote 71 Although there is concern that because masks are loose fitting they may allow the escape of aerosols (particularly during coughing), tight-fitting respirators may be uncomfortable for patients (particularly those with limited respiratory reserve) and are therefore not recommended for source control.

Airborne precautions for a patient with symptoms of respiratory TB can be discontinued once suspicion of TB is appropriately excluded, based on results of microbiological investigation and establishment of an alternate diagnosis.

Although the degree and duration of infectiousness of patients after initiation of effective therapy remains unclear, it is known that effective therapy will rapidly reduce cough and the number of viable mycobacteria in the sputum. In patients who are no longer able to spontaneously produce a sputum specimen, sputum induction is useful and appropriate. A poor response to therapy should raise the possibility of drug resistance, even before susceptibility results are available, and inform the decision on discontinuing precautions.

Most people with respiratory TB can be managed in the outpatient setting. If hospitalization is needed, patients with TB are not necessarily required to remain in hospital until no longer infectious. While smear-positive patients are still potentially infectious, their household contacts have already been exposed and are often receiving therapy for latent TB infection when discharge from hospital is being considered. The risk of transmission to these contacts should be balanced by the social, mental and physical health benefits of the patient's return home. Patients with TB should be discharged as soon as there is no further medical indication to continue hospitalization and criteria for home isolation are met (see Appendix B: De-isolation review and recommendations).

On the one hand, there is no evidence of TB being transmitted from persons who have received at least 2 weeks of effective anti-TB therapy. On the other hand, the evidence of no transmission is of poor quality. Given the uncertainty that arises from poor evidence and the potential exposure of highly susceptible contacts (e.g., very young children or highly immune-compromised patients), especially within the acute care hospital setting, the decision to discontinue airborne precautions is individualized. As such, airborne precautions may be continued for a longer period of time in hospital, where many patients are immune-compromised, than is the case in community settings.

Recommendations:

Good practice statements:

4.1.5. Transport of patients with, or being evaluated for, respiratory TB

There is a potential for exposure to, and transmission of, TB during patient transport that can be prevented by applying appropriate IPC measures.

Good practice statements:

4.1.6. Education of health care workers

An important component of any TB IPC Program is HCW education on how to recognize and protect themselves from exposure to M. tuberculosis. This includes information on epidemiologic and medical risk factors for TB, signs and symptoms of TB (respiratory and non-respiratory), mechanisms of transmission and principles of control.Footnote 72

Recommendations:

4.1.7. Health care worker testing and treatment for TB infection

The importance of conducting a baseline HCW assessment for the presence of latent TB infection cannot be overemphasized. At the time of employment, there may be HCWs with latent TB infection because of prior exposure, particularly the situation for HCWs born or previously living in high-TB-incidence countries (see Appendix 2, Table 2a).Footnote 4Footnote 6Footnote 37Footnote 73 Foreign-born HCWs represent an increasing proportion of the workforce in Canadian hospitals and long-term care homes.Footnote 74 HCWs with reactivation of a latent TB infection can be a source of TB transmission in the healthcare setting where they work.Footnote 6Footnote 75 As per the evidence summary in Appendix 1, Table 1a and Table 1b, 7 out of 16 identified exposure events were due to an index HCW case. Testing and treating for TB infection is expected to reduce this source of exposures.

Historically, the tuberculin skin test (TST) has been the standard for making a diagnosis of latent TB infection. More recently, interferon-gamma release assays (IGRAs) have been introduced as another diagnostic test. However, the use of IGRA for serial (repeated) testing of HCWs is not recommended because serial-testing studies have shown high rates of conversions and reversions, unrelated to exposure or treatment (see Chapter 4: Diagnosis of tuberculosis infection).

Prior exposure to M. tuberculosis or Bacille Calmette-Guérin (BCG) vaccination can result in a boosting phenomenon due to immune recall to a mycobacterial antigen, which may be misdiagnosed as a TST conversion. Interpreting a positive TST performed as part of contact tracing in response to a potential TB exposure in an individual with preexisting latent TB infection or BCG vaccination and for whom an employment test result is unknown can incorrectly over-count TST conversions in relation to a healthcare exposure event. Therefore, a 2-step TST is recommended to establish baseline (see Chapter 4: Diagnosis of tuberculosis infection).Footnote 4Footnote 76

Studies from the United States and the United Kingdom indicate that HCWs in low-incidence countries are at no higher risk for TB than the general population, when adjusted for country of origin (see Appendix 2, Table 2b).Footnote 4Footnote 6Footnote 77 As such, there is no indication for routine organization-wide periodic TST of all HCWs.Footnote 29Footnote 76 Periodic screening (e.g., annual testing) of HCWs at higher risk for occupationally acquired TB, based on the organization risk assessment, may be warranted. Examples of such situations might be HCWs working in bronchoscopy suites or on units identified as having exposure episodes.

Any HCW identified as having had unprotected exposure (termed an exposure episode) to a patient/resident/client or coworker confirmed to have respiratory TB disease should be assessed for TB infection (see section 9 in this chapter and Chapter 11: Tuberculosis contact investigation and outbreak management).

Recommendations:

Good practice statements:

5. Personal protective equipment

The PPE tier refers to the availability and appropriate use of protective equipment that a susceptible host may wear to provide a physical barrier between them and an infectious agent/infected source. The use of PPE is dependent on HCW adherence and competence and, as a result, is the control that is most easily compromised.Footnote 45 Use of respirators is addressed in section 4.1.2.

6. Prevention of transmission of M. tuberculosis in specific units and populations within hospitals

6.1. Specific units

In certain units (e.g., chemotherapy, HIV and dialysis units), there may be a greater number of patients at higher risk for TB or at greater risk for acquiring TB if exposed (see Chapter 4: Diagnosis of tuberculosis infection and Chapter 10: Treatment of active tuberculosis in special populations). Special consideration is required to prevent the transmission of TB to HCWs, other patients and visitors in such units.

Good practice statement:

6.2. Special populations

There are certain individuals whose immunocompromising conditions or immunosuppressive therapy places them at higher risk of progression from TB infection to disease. They include HIV-infected individuals, transplant patients and people undergoing anti-tumor necrosis factor therapy. While TB incidence rates in patients with end-stage kidney disease are higher than those in the general population and symptoms of respiratory TB may be atypical, case numbers are low.Footnote 78 Providing care for immune-compromised patients requires a higher index of suspicion for TB and increased vigilance to prevent its transmission before diagnosis. Screening for latent TB infection is recommended for selected high-risk populations (see Chapter 4: Diagnosis of tuberculosis infection and Chapter 10: Treatment of active tuberculosis in special populations).

7. Prevention of transmission of M. tuberculosis within other healthcare settings

Although the principles of TB IPC found in Sections 2 through 6 inclusive are the same across the continuum of healthcare, there is variation in transmission risk and availability of control measures associated with different settings. Modification of control measures applied, and alternative strategies may be required. This section identifies additional specific considerations for non-hospital settings.

7.1. Long-term care homes

Residents of long-term care (LTC) homes are considered to be at the same risk for having latent TB infection as other populations in the community, and have the same risk of developing active TB as persons of the same age in the general population, with the exception of those belonging to identified at-risk groups (see Chapter 6: Tuberculosis Preventive Treatment in Adults, Table 1). However, because of the concern for transmission of TB in LTC homes and the anticipated need for contact tracing should there be an exposure, many guidelines recommend screening newly admitted residents.

Across the Canadian provinces and territories, practices around assessment of new admissions for TB vary. In some provinces/territories, pre-admission and admission screening for symptoms and/or risk of active TB are recommended or mandated. In many provinces, screening for latent TB infection is recommended with a TST and/or chest x-ray, but the criteria for testing vary from all new residents to those who are at increased risk for TB. Some jurisdictions stipulate that the decision for screening should be based on a facility risk assessment and local epidemiology. For discussion and recommendations regarding testing for TB infection in this population, see Chapter 4: Diagnosis of Tuberculosis Infection.

Good practice statements:

7.2. Ambulatory care/outpatient clinics

Ambulatory care settings include locations where health services are provided to patients who are not admitted to inpatient hospital units. This includes, but is not limited to, outpatient diagnostic and treatment facilities (e.g., diagnostic imaging, phlebotomy sites, pulmonary function laboratories, TB treatment facilities), community health centers or clinics, physician offices and offices of allied health professionals (e.g., physiotherapists).Footnote 25Footnote 45

Good practice statements:

7.3. Remote and isolated healthcare settings

In remote and isolated communities there are many challenges to TB IPC. Resource limitations may result in difficulties with access to adequate diagnostic facilities for bacteriologic examinations and chest x-ray. A high index of suspicion for a patient having respiratory TB is required. If a chest x-ray is difficult to organize because patients must fly out of the community, then sending sputum samples for TB smear and culture, or nucleic acid amplification test, may be a more rapid way to make a diagnosis of respiratory TB, with less risk of transmission to others. Cohorting may need to be considered as a strategy to accommodate inpatients with respiratory TB if there are insufficient numbers of AII or private rooms.

Recommendations:

Good practice statements:

7.4. Home care settings

Home care is delivered to patients who reside in their home or a community care residence. M. tuberculosis transmission to HCWs who work in home-based healthcare settings has been documented, with recommendations developed to prevent transmission.Footnote 25

Good practice statements:

8. Prevention of transmission of M. tuberculosis within congregate settings

In some congregate settings, such as correctional facilities, homeless shelters or hospices there may be a higher proportion of persons with risk factors that put them at greater risk of developing TB, with subsequent transmission to others. The principles and recommendations for preventing transmission of TB in healthcare settings can inform TB IPC policies and procedures for congregate settings.

9. Contact tracing in healthcare settings

While there are many publications regarding outbreak investigations and the outcome of contact tracing efforts arising from TB exposures in the healthcare setting, there is much variation in the exposure criteria used, the extent and duration of the investigation and the diagnostic tests used (see Appendix 1). Most contact investigations following healthcare-associated exposures find few secondary cases of either active or latent TB.Footnote 10 Despite that, there is the expectation that health care organizations will undertake appropriate contact tracing and a need for relevant contact-tracing guidance in this setting.

Contact tracing following identification of a patient/resident with TB who has not been on airborne precautions or a HCW with TB who worked while infectious must be undertaken in an organized, systematic fashion and in close collaboration with local public health authorities.

Contact tracing principles and steps are described in Chapter 11: Tuberculosis contact investigation and outbreak management, including determination of infectiousness of the index case, likely period of infectiousness, degree of exposure and prioritization of contacts for screening and evaluation. Although the principles are the same in healthcare settings, there are some specific considerations.

Assessment of exposure: Exposure of HCWs or other patients is to be considered if they shared space with a patient with respiratory TB who was not on airborne precautions for any period of time during the infectious period. Exposure can also occur when an aerosol-generating medical procedure (e.g., high-pressure wound irrigation, procedure using power tools or cautery) is performed at or near the site of extra-pulmonary TB without airborne precautions.

Contact priority: In a typical contact investigation approach, contacts are classified as high-, medium- and low-risk priority, based on level of exposure and risk of progression to active disease.

In healthcare settings, the following are considered high-priority:

Initial investigation of contacts: In healthcare settings, it is typical to use somewhat lower thresholds for the initial contact investigation compared to the community, because of potential vulnerability of the patient population and risk for further transmission in the healthcare setting. However, it is still important to have a risk-based approach and not to include patients/residents and HCWs with minimal or no exposure whose risk of infection is negligible, and in whom screening could cause more harm than benefit.

The exact duration of exposure that defines a significant risk for acquiring TB is not defined. There is general agreement that any duration of exposure to an aerosol-generating medical procedure warrants contact tracing. Individual facility policies for contact tracing in healthcare settings have used exposure durations in non-aerosol-generating medical procedure situations that vary between two and 48 hours, modulated by the index case's level of infectiousness, facility ventilation and the contact's risk of developing active TB. In hospital settings, it may be useful to measure air change rates in the exposure areas, to help prioritize contacts. It is important to remember the need to expand an investigation to include a shorter cumulative duration of exposure if transmissions have been identified during the initial investigation. Outcomes for the investigation across all settings (healthcare and community) should be pooled to guide decisions around expanding the investigation. Table 3 provides a framework for establishing exposure thresholds for contact investigations in acute care settings, based on a range of exposure durations used by different jurisdictions. No evidence is available to recommend the use of a specific threshold.

Table 3. Suggested framework for TB transmission risk algorithm and contact follow-upFootnote a
Transmission risk factors Transmission risk level Criteria for contacts
Patient with low risk of progression to active TB Patient with high risk of progression to active TB Staff
Aerosol-generating medical procedure Very high Not applicable Not applicable Any staff present without appropriate personal protective equipment
Laryngeal TB Very high 2-12 hours of cumulative exposure in shared air space 2-3 hours of cumulative exposure in shared air space ≥12 hours of cumulative exposure in shared air space

Smear-positive respiratory TB
or
cavitation on chest x-ray

High 4-24 hours of cumulative exposure in shared air space 2-12 hours of cumulative exposure in shared air space 4-36 hours of cumulative exposure in shared air space

Smear-negative respiratory TB
and
no cavitation on chest x-ray

Low 20-48 hours of cumulative exposure in shared air space 4-24 hours of cumulative exposure in shared air space 20-60 hours of cumulative exposure in shared air space

Footnotes:

Footnote a

Framework adapted from St. Michael's Hospital (Toronto) Exposure Investigation Guidelines for Patients and Staff Exposed to Pulmonary Tuberculosis (personal communication MP Muller) and Toronto Public Health's Structured Risk-based Tool for Contact Investigations (see Chapter 11: Tuberculosis contact investigation and outbreak management). The framework was expanded to include range of exposure durations used by other jurisdictions.

Return to footnote a referrer

Acknowledgments

Employees of the Public Health Agency of Canada:

The following members of the Public Health Agency of Canada's National Advisory Committee on Infection Prevention and Control for review of the chapter:

Molly Blake, RN, BN, MHS, CIC
Program Director, Infection Prevention and Control | WRHA (Winnipeg Regional Health Authority)
Acting Program Director, Medical Device Reprocessing | WRHA Winnipeg, MB
Nan Cleator, RN
National Practice Consultant (formerly)
Practice Quality and Risk Team
Victorian Order of Nurses (VON) Canada
Bracebridge, ON
Joanne Embree, MD, MSc
Pediatric Infectious Disease Specialist, Shared Health
Professor, University of Manitoba
Winnipeg, MB
Jennifer Happe, BSc, MSc
Infection Control Professional
Alberta Health Services
Director, Infection Prevention and Control Canada
Red Deer, AB
Susy Hota, MD, MSc, FRCPC
Medical Director, Infection Prevention and Control
University Health Network
Associate Professor, Department of Medicine, Division of Infectious Diseases
University of Toronto
Toronto, ON
Jennie Johnstone, MD, PhD, FRCPC
Medical Director IPAC, Sinai Health
Toronto, ON
Anne Masters-Boyne, RN, MN
Employee Health Services at Horizon Health Network
Fredericton, NB
Matthew Muller, MD, PhD, FRCPC
Assistant Professor, University of Toronto
Medical Director, Infection Prevention and Control, Unity Health Toronto Toronto, ON
Patsy Rawding, RN, BScN, CIC
Health Services Manager, Infection Prevention and Control
Western Zone, NSHA Lead Manager in LTC
Middleton, NS
Suzanne Rhodenizer, RN, BScN, MHS, CIC
Director, Clinical Planning
IPAC Consultant QEII New Generation Project
Nova Scotia Health
Halifax, NS
Brian Sagar
Senior Director, Communicable Disease
British Columbia Ministry of Health
Victoria, BC
Patrice Savard, MD, MSc, FRCPC
Clinical Associate Professor, University of Montreal
Clinical Microbiologist and Infectious Diseases Specialist, CHUM Medical Director, Nosocomial Infection Prevention and Control Unit, CHUM
Montréal, QC
Nisha Thampi, MD, MSc, FRCPC
Medical Director, Infection Prevention and Control Program, Division of Infectious Diseases
Children's Hospital of Eastern Ontario
Associate Professor, Department of Pediatrics, University of Ottawa
Ottawa, ON

Disclosure statement

The Canadian Thoracic Society (CTS) TB Standards editors and authors declared potential conflicts of interest at the time of appointment and these were updated throughout the process in accordance with the CTS Conflict of Interest Disclosure Policy. Individual member conflict of interest statements are posted on the CTS website.

Funding

The 8th edition Canadian Tuberculosis Standards are jointly funded by the CTS and the Public Health Agency of Canada, edited by the CTS and published by the CTS in collaboration with the Association of Medical Microbiology and Infectious Disease (AMMI) Canada. However, it is important to note that the clinical recommendations in the Standards are those of the CTS. The CTS TB Standards editors and authors are accountable to the CTS Respiratory Guidelines Committee (CRGC) and the CTS Board of Directors. The CTS TB Standards editors and authors are functionally and editorially independent from any funding sources and did not receive any direct funding from external sources. The CTS receives unrestricted grants which are combined into a central operating account to facilitate the knowledge translation activities of the CTS Assemblies and its guideline and standards panels. No corporate funders played any role in the collection, review, analysis or interpretation of the scientific literature or in any decisions regarding the recommendations presented in this document.

Appendix 1: Summary of available evidence

Table 1a. Epidemiological investigations reporting TB exposures in healthcare settings, linked to a health care worker index case
Author, ref, year Setting, country Index/source case characteristics Transmission (Yes/No) and associated risks Study population and contact investigation details TB/LTBI screening and testing Transmission outcomes
Acute care settings
BalmelliFootnote 15
2014
Acute care hospital
Switzerland
Index: HCW from a high TB endemic region found to be infectious due to abrupt onset of productive cough, weakness, and malaise

No

HCW did not undergo pre-employment TB screening; lack of baseline TST data limited HCW exposure assessments

All HCW and patients in contact with index for any period of time in the 2 weeks before symptom onset Questionnaire on demographics, risk factors and duration of contact with index case, 2 step TST, IGRA

Active TB cases linked to exposure event: None

TST conversions linked to exposure event: 6 to 10/101 HCW and patient contacts (variability in 2 step TST and IGRA conversions)

OrensteinFootnote 35 2013 Acute care hospital
Canada
Index: HCW dx with active TB, assumed to be infectious for 6 months prior to diagnosis

No

Delivery of care by a HCW with an active TB infection to Oncology and Palliative care patients

All HCWs in contact with index case; all patient and family contacts Not reported

Active TB cases linked to exposure event: None

TST conversions linked to exposure event: 9/121 HCW contacts

HazardFootnote 13 2016 Acute care hospital, nutritional service department employees
United States
Index: HCW with no patient contact

Yes

Kitchen located in a confined basement of the facility with a dedicated exhaust system independent from healthcare facilities other ventilation systems

All current and former (previous 6 months) staff (limited to kitchen) included in CI; Routine HCW TB screening identified a high frequency of TST conversions in nutritional service employees prompting a CI Symptom questionnaire, 2 step TST, clinical assessment of contacts with previous positive TST results

Active TB cases linked to exposure event: 4 HCW contacts (nutritional service staff). 1 HCW was identified with MTB + sputum 4 years post exposure event, TST negative during CI and annual screening

TST conversions linked to exposure event: 20/224 nutritional service staff contacts

Index case confirmed by spoligotype and MIRU

MerteFootnote 38
2014
Dental Clinic
United States
Index: HCW with active pulmonary TB, female, mid-40 yrs, known untreated LTBI, lived in a high TB endemic region, cough, fever, fatigue, weight loss; 4+ AFB, CXR indicative of infection

No

Lack of baseline TST data limited HCW exposure assessments, HCW worked for approx. 6 months while infectious

HCW, patients, and household contacts of index; 462 patient contacts without previous documented TST Symptom questionnaire, 2 step TST, clinical evaluation and CXR for contacts with previous positive TST results

Active TB cases linked to exposure event: None

TST conversions linked to exposure event: 1/19 HCW contacts, 0/1 household contact

RomagnoliFootnote 36 2012 Acute care hospital, Neonatology unit
Italy
Index: HCW who worked at multiple healthcare facilities

Yes

None reported

All Patient in the maternity ward 3 months before the birth of the index case and 2 days after the last working day of the HCW with active TB IGRA for newborn contacts > 12moa, and follow-up test at 3 moa; TST, CXR and clinical assessment for contacts with documented positive TST results

Active TB cases linked to exposure event: 1 Patient. dx. with pulmonary extra-pulmonary TB at 4 moa at another hospital

TST conversions linked to exposure event: None

Active TB cases matched by DNA finger printing

Long-term and residential care settings
KhalilFootnote 11 2013 Long-term care and residential care facility
Canada

Index: HCW presenting with cough, fever, night sweats, and pleuritic chest pain; immigrant from an endemic region; Baseline TST at hire was documented to be negative

Source case: Chart review suggests a resident with active TB may have been symptomatic up to 12 months prior to dx.

Yes

Patient care to residents; Baseline TST at hire available for 40% of staff; Ventilation in a tested dining room, common room, and most resident rooms <4 ACH

Residents or staff (including volunteers) who shared indoor airspaces daily and/or >4 hr per week with index case; Family members or visitors who shared indoor airspaces for >2-4 hr per week with index case 2 step TST, CXR for TST positive contacts, and suspicious CXR followed up with chest computerized tomography scan and sputum samples
for culture; concentric circle approach to CI

Active TB cases linked to exposure event: 3 resident contacts

TST conversions linked to exposure event: 9/121 HCW contacts, 15/146 resident contacts, none among visitor and household contacts

Active TB cases matched by genotyping

MorFootnote 37
2018
Nursing Home
Israel
Index: HCW from a high TB endemic region found to be infectious following productive cough, fever, malaise, weakness and loss of appetite

Yes

Patient care to residents; HCW CXR abnormal but permitted to work at facility

Resident and staff contacts of index case Symptom screen interview, 2 step TST, concentric circle approach to CI

Active TB cases linked to exposure event: 1 HCW contact and 2 resident contacts

TST conversions linked to exposure event: 26/68 resident contacts, 2/32 HCW contacts

Abbreviations:
ACH, air changes per hour; AFB, acid-fast bacillus; CI, contact investigation; CXR, chest radiograph; DNA, Deoxyribonucleic acid; dx, diagnosis; HCW, health care worker; IGRA, interferon-gamma release assay; LTBI, latent TB infection; MIRU, mycobacterial interspersed repetitive units; moa, months of age; MTB, mycobacterium tuberculosis; TST, tuberculin skin test

Table 1b. Epidemiological investigations reporting TB exposures in healthcare settings, linked to a patient or long-term care resident (patient) index case
Author, ref, year Setting, country Index/source case characteristics Transmission (Yes/No) and associated risks Study population and contact investigation details TB/LTBI screening and testing Transmission outcomes
Acute care settings
BucherFootnote 17 2016
FreytagFootnote 39 2016Footnote a
Acute care hospital
Germany and United States

Source: Patient. organ donor treated for TB 40+ years ago, no recent TB symptoms identified

Index: Patient. 70 yrs, kidney organ recipient, clinical deterioration at 6 weeks post transplant

Index: Patient. 60 yrs, liver transplant recipient, died from TB infection 15.5 months post transplant

Yes

Donor derived TB not considered among solid organ transplant recipients; AGMP and invasive medical procedures (e.g. surgical wound debridement, general anesthesia, endotracheal intubation) performed without airborne precautions

Individuals cumulatively exposed to the index patient >40hrs or continuously for >8hrs Not reported

Active TB cases linked to exposure event: 1 HCW contact. This HCW was excluded from the initial post exposure CI

TST conversions linked to exposure event: Not Reported

Active TB cases matched by WGS

de PerioFootnote 23 2014 Acute care hospital
United States
Index: Patient. with pulmonary TB, AFB positive, reported to have difficulty hearing (i.e. required close interactions to interpret communications)

Yes

Delay in TB dx. and initiation of IPC measures; patient care (e.g. ED evaluation) performed without airborne precautions; NIOSH assessment identified issues with AIIR pressure sensor calibrations, ACH, direction of air flow and pressure differential (several AIIR did not meet CDC recommendation); doors between anteroom and hallways open when AIIR were occupied

HCW with a TST conversion during outbreak year or self-reporting exposure to index patient; HCW exposures identified by shift records TST, AFB, staff interviews

Active TB cases linked to exposure event: 1 HCW contact (nursing assistant); 1 household contact (spouse of index case)

TST conversions linked to exposure event: 19/41 HCW contacts

Report Active TB cases to be related

Grisaru-SoenFootnote 14 2014 Acute care Children's hospital
Israel
Index: Patient. 26 day old premature infant with congenital TB, 5 day history of recurrent vomiting and respiratory failure at admission, mother originating from endemic region with suspect diagnosis for pulmonary TB

Yes

Delay in TB dx. and initiation of IPC measures; AGMP and patient care (e.g. mechanical ventilation, bronchoalveolar lavage) performed without airborne precautions

NICU PICU patients, staff, or visitors >24 in the same room as index case TST contacts >5 years of age; physical examination for contacts <3 months of age; CXR; 2 step TST for adult contacts

Active TB cases linked to exposure event: 1 (mother of infant)

TST conversions linked to exposure event: 3/35 staff contacts, 1/75 NICU and PICU patient contacts, 3/22 PICU visitors, 8/58 NICU visitors

HoldenFootnote 18 2018 Acute care hospital, ER and ICU
United Kingdom
Index: Patient. 50 yrs, lower respiratory tract infection, history of sustained weight loss, productive cough at admission, marginally housed, CXR showed cavitation

Yes

Delay in TB dx. and initiation of IPC measures due to misdiagnosis of pneumonia, AGMP and patient care performed without airborne precautions, Discontinuation of airborne precautions without considering symptoms after 14 days of anti-TB treatment.

All HCW with
>4hrs of contact with index Patient, HCW present during AGMP or in close proximity during invasive procedures; family members of HCW with active TB; concentric circle approach to CI
Symptoms questionnaire, IGRA, CXR

Active TB cases linked to exposure event: 1 HCW contact. This HCW was excluded from the initial post exposure CI

TST conversions linked to exposure event: 7/8 ICU HCW contacts

Active TB cases matched by WGS

JonssonFootnote 24 2013
KanFootnote 40 2013Footnote a
Acute care hospital
Denmark
Index: Patient. 50 yrs, HIV+, history of IDU, 6 week history of coughing and weight loss at admission, died at hospital

Yes

Delay in TB dx. and initiation of IPC measures due to misdiagnosis of pneumonia, AGMP (e.g. bronchoscopy) and patient care performed without airborne precautions, discontinuation of airborne precautions without sputum analysis results, lack of baseline TST data limited HCW exposure assessments, socialization among ward patients, shared patient rooms, personal care assistance to roommate of index

Initial CI was limited to HCW with major exposure to index patient, then expanded to include all HCW at the ward TST, IGRA, CXR

Active TB cases linked to exposure event: 3 HCW contacts; 4 patient contacts. 1 HCW was excluded from the initial post exposure CI

TST conversions linked to exposure event: 15/36 HCW contacts, 4/15 patient contacts, 5/7 social contacts.

Some active TB cases matched by RFLP

KhatamiFootnote 34 2017 Acute care Children's hospital and pediatric operating room
Australia
Index: Patient. 12 yrs male; 5 day history of acute onset fever, dyspnea, cough, and malaise at admission; CXR abnormal

No

Delay in TB dx. and initiation of IPC measures; AGMP and patient care performed without airborne precautions (e.g. daily chest physiotherapy, general anesthesiology, video-assisted thoracoscopic surgery, frequent blood collection, chest drain, central venous catheter insertion, bronchoalveolar lavage); shared patient rooms; lack of baseline TST data limited HCW exposure assessments

HCW assessed to be close contacts of index case; patients who shared a room with the index case >8 hrs; concentric circle approach to CI 2 step TST and IGRA, CXR and assessment at chest clinic for contacts with documented positive TST

Active TB cases linked to exposure event: None

TST conversions linked to exposure event: Initial CI group 4/38 HCW contacts and expanded CI group 2/51 HCW contacts (physiotherapists and anesthesiologists)

MedranoFootnote 12 2014 Acute care hospital
United States

Index: Patient. mid 20 yrs, HIV+, history of being marginally housed, prison inmate admitted to hospital, died at hospital, previously infected and treated for another TB strain, PCR positive for MTB but no viable samples for genotyping

Source: inmate from the same jail who shared the same holding cell for <10 hrs

Yes

Delay in TB dx. and initiation of IPC measures due to misdiagnosis of pneumonia; inadequate respiratory risk assessment at admission; patient often walked the halls of the hospital floor

All HCW, correctional staff, patients, and visitors to the floor housing the index case

NOTE: Routine HCW TB screening identified a high frequency of TST conversions prompting the CI

TST, IGRA, TB symptom screen for contacts with documented positive TST results, CXR and sputum culture for symptomatic contacts

Active TB cases linked to exposure event: 3 HCW contacts (2 nurses and a social workers); 6 other hospital contacts (patients, visitors, correctional staff)

TST conversions linked to exposure event: 87/318 of all hospital contacts; 23/30 HCW contacts (on the same floor as index case); 12/67 patient and visitor contacts

Active TB cases (with positive culture results) matched by WGS

TownesFootnote 41 2016 Ambulatory care
United States
Index: Patient. at Rheumatology clinic on immunosuppressive medication, cough

No

Delay in TB dx. and initiation of IPC measures due to misdiagnosis of pneumonia; inadequate respiratory risk assessment at clinic visit

Anyone who shared the clinic airspace with index case >2hrs Symptom assessment; 2 step TST and/or IGRA; CXR and symptom assessment for contacts with previous positive IGRA results

Active TB cases linked to exposure event: None

TST conversions linked to exposure event: None among HCW and patient contacts; 7/17 community contacts

Long-term and residential care settings
HarrisFootnote 22 2013 Long-term care facility joined to an Acute care hospital
United States
Index: LTC resident 68 yrs, male with a history of laryngeal cancer, diabetes, hypertension, COPD, cerebrovascular accident, abnormal CXR 9 months prior to TB dx.

Yes

Delay in TB dx. and initiation of airborne precautions; AGMP without airborne precautions (e.g. repeated mucus/secretion suction, routine tracheostomy care; re-insertion of tracheostomy tube); shared negative pressure room <2-3hrs ACH with airflow from index to secondary case; group dinning and recreation activities among LTC residents

Resident/patient, visitor and staff contacts of index case in LTC (ventilator-dependent care and sub-cute care units); Hospital staff and patient contacts of index case TST and IGRA, sputum sample culture, clinical assessment, CXR recommended for LTC contacts

Active TB cases linked to exposure event: 2 resident contacts (a roommate of index case, and a resident of a room across the hall from index at LTC site)

TST conversions linked to exposure event: 7/64 patient or resident contacts, 5/239 HCW contacts (LTC staff). No TST conversions among hospital contacts

Active TB cases matched by RFLP

Abbreviations:
ACH, air changes per hour; AFB, acid-fast bacillus; AGMP, aerosol-generated medical procedure; AIIR, airborne infection isolation room; CDC, Centers for Disease Control and Prevention; CI, contact investigation; CXR, chest radiograph; COPD, chronic obstructive pulmonary disease; dx, diagnosis; ED, emergency department; ER, emergency room; HCW, health care worker; HIV, human immunodeficiency virus, ICU, intensive care unit; IDU, injecting drug user; IGRA, interferon-gamma release assay; IPC, infection prevention and control; LTBI, latent TB infection; LTC, long-term care; MTB, mycobacterium tuberculosis; NICU, neonatal intensive care unit; NIOSH, National Institute for Occupational Safety and Health; PCR, polymerase chain reaction; PICU, pediatric intensive care unit; RFLP, Restriction fragment length polymorphism; TST, tuberculin skin test; WGS, whole genome sequencing

Footnotes:

Footnote a

Companion articles. Articles identified as companion articles provide supplementary information about a specific epidemiological investigation. Where such articles exist, the additional information is included in the table.

Return to footnote a referrer

Table 1c. Observational studies reporting on TB exposures in healthcare settings
Author, ref, year Setting, country Study population Transmission (Yes/No) and associated risks Transmission outcomes
UppalFootnote 20 2014 Acute care hospital
Canada
All HCW, Patient and Visitor exposures to active TB cases (n = 15) at the hospital in 2011; Ten significant exposures identified among (n = 7) active TB infections

No

Delay in TB dx. and initiation of airborne precautions; Advanced age, atypical presentation of TB infection, comorbid infections, errors in ordering and interpreting microbiological or CXR results

Root cause analysis found 70% of the significant exposure incidents among active TB patients were linked to delay in TB dx. and initiation of airborne precautions

No TST conversions among HCW following significant exposures identified

de VriesFootnote 16 2017 Not specified
Netherlands
HCW with TB identified in a national registry (n = 131), analysis of factors contributing to infection transmission from patients to HCW Delay in TB dx. led to TB infection transmissions among 47% of HCW in the sample

24% of TB cases (n = 32) in registry were categorized as transmissions in healthcare settings, between patients and HCW; majority linked to delays in TB dx.

Roles of HCW infected with TB at the workplace were nurse (n = 15), medical doctor (n = 6), bronchoscopy assistant (n = 3), autopsy assistant (n = 3), medical equipment sterilisation assistant (n = 2), laboratory assistant (n = 1), pathology assistant (n = 1), and medical assistant (n = 1)

MuzziFootnote 21 2014 Acute care hospital
Italy
HCW exposures (n = 388) to pulmonary and respiratory TB patients (n = 14) due to delayed dx. or airborne precautions Patient comorbidities linked to delayed dx. cirrhosis, advanced cancer, chronic kidney disease, HIV and diabetes TST conversions linked to exposure event:
3.7% (n = 9) of exposed HCW assumed TST negative at baseline (n = 255), were positive at 3 months post exposure by 2 step TST
SchepisiFootnote 10 2015 Various acute and outpatient healthcare settings
Multiple countries
HCW diagnosed with respiratory active TB (n = 177) among studies reporting confidence interval outcomes

Yes

Medical procedures linked to transmission were tooth extractions and hemodialysis

Meta-analysis estimated active TB among exposed individuals to be: 0.11% (95% Confidence Interval 0.04–0.21) for infants, 0.38% (95% Confidence Interval 0.01–1.60) for children, 0.09% (95% Confidence Interval 0.02–0.22) for adults and 0.00% (95% Confidence Interval 0.00–0.38) for HCWs.
Abbreviations:
HCW, health care worker; TST, tuberculin skin test; dx, diagnosis; CXR, chest radiograph; HIV, human immunodeficiency virus; n, number.

Appendix 2: Available supporting body and quality of evidence for recommendations and good practice statements

Table 2a. Tuberculosis (TB) exposures in healthcare or long-term care settings linked to absent or sub-optimal baseline TB screening in health care workers (HCWs)
Research question: Have absent or sub-optimal baseline TB screening in HCWs been linked to TB exposures in healthcare or long-term care facilities?Footnote a
Study Setting Transmission Study design Quality Directness Critical appraisal resultsFootnote b
BalmelliFootnote 15 2014 Acute No Weak Medium Direct Study Number: Three epidemiological investigations provide limited evidence of a TB exposure from an infectious HCW in a health care setting, and link exposures to absent or sub-optimal baseline TB screening. Furthermore, Jonsson et al. reports that a contact investigation of exposed HCW was limited due to missing baseline tuberculin skin test data.
Study Quality: The identified studies were assessed to be of low to medium quality by two appraisers.
Consistency of Results: Three studies consistently identified missing or sub-optimal screening of HCWs upon hire as primary and attributed causes of exposure. This evidence is considered consistent.
Directness: These studies report missing or sub-optimal baseline screening of HCW to have led to TB transmission from infectious HCWs to colleagues and other patients. The remaining study (Jonsson et al.) provides indirect evidence that baseline TB testing data is valuable to post-exposure contact investigations.
Generalizability: Overall, this evidence is generalizable to Canadian hospital and long-term care settings.
Strength of Body of Evidence: Weak to Moderate
KhalilFootnote 11 2013 LTC Yes Weak Low Direct
MorFootnote 37
2018
LTC Yes Weak Low Direct
JonssonFootnote 24 2013 Acute Yes Weak Medium Extrapolation
Overall - - Weak Low - medium Direct

Abbreviations:
HCW, health care worker; LTC, long-term care

Footnotes:

Footnote a

This body of evidence informs Chapter 14 recommendations on HCW testing and treating for TB infection.

Return to footnote a referrer

Footnote b

Rating the quality of the overall body of available evidence for specific recommendations was conducted using the Public Health Agency of Canada Critical Appraisal Toolkit (CAT). Moralejo D, Ogunremi T, Dunn K. Critical Appraisal Toolkit (CAT) for assessing multiple types of evidence. Can Commun Dis Rep. 2017;43(9):176-81. https://doi.org/10.14745/ccdr.v43i09a02

Return to footnote b referrer

Table 2b. Tuberculosis (TB) risk (latent or active TB infection) among health care workers (HCWs) compared to non-HCW populations in low-incidence countries
Research question: Is TB risk (latent or active TB infection) among HCWs in low-incidence counties higher when compared to the general population?Footnote a
Study Country HCW vs. non-HCW Study design Quality Directness Critical appraisal resultsFootnote b
DielFootnote 77 2018 Germany Higher TB risk Weak Medium Extrapolation Study number: Five studies report on TB risk among HCWs vs. non-HCW or general population groups. Three studies used population-based surveillance data, providing direct evidence that TB risk is similar between HCWs and non-HCWs, and any identified differences were not statistically significant. Two studies provide evidence that can be extrapolated to describe TB risk among HCWs. Youakim compared TB occupational compensation claims in British Columbia, Canada from 1999-2008, and found registered nurses to be at increased risk of TB infection claims, compared to other occupation groups. An analysis of TB clusters by Diel et al. found HCW were more likely to be associated with a case cluster linked to transmission at work, compared to non-HCWs.
Study quality: Included studies were assessed to be of medium quality
Consistency and directness of results: The three studies providing direct evidence are consistent, concluding no evidence of elevated TB risk among HCWs, compared to non-HCWs. Two studies provide evidence that can be inferred to suggest that HCWs, such as nurses, are at increased risk for occupational TB exposures and transmissions.
Generalizability: Overall, this evidence is generalizable to Canadian hospital and long-term care settings.
Strength of body of evidence: Moderate
Note: A systematic review by the World Health Organization found TB risk to be elevated among HCW compared to the general public in high and low burden countries. However, this review was not limited to recent evidence (inclusion criteria: studies published after 1946)
DavidsonFootnote 4 2017 United Kingdom Similar TB risk Moderate Medium Direct
GehannoFootnote 9 2017 France Similar TB risk Weak Low Direct
LambertFootnote 6 2012 United States Similar TB risk Weak Medium Direct
YouakimFootnote 8 2016 Canada Higher TB risk Weak Medium Extrapolation
Overall - Similar TB risk Weak Medium Direct

Abbreviations:
HCW, health care worker

Footnotes:

Footnote a

This body of evidence informs Chapter 14 recommendations on HCW testing and treating for TB infection.

Return to footnote a referrer

Footnote b

Rating the quality of the overall body of available evidence for specific recommendations was conducted using the Public Health Agency of Canada Critical Appraisal Toolkit (CAT). Moralejo D, Ogunremi T, Dunn K. Critical Appraisal Toolkit (CAT) for assessing multiple types of evidence. Can Commun Dis Rep. 2017;43(9):176-81. https://doi.org/10.14745/ccdr.v43i09a02

Return to footnote b referrer

Table 2c. Tuberculosis (TB) exposures linked to delayed diagnosis and initiation of airborne precautions in patients or residents
Research question: Have delayed diagnosis of TB and initiation of airborne precautions in patients or residents been linked to TB exposures in healthcare or long-term care facilities?Footnote a
Study Setting Transmission Study design Quality Directness Critical appraisal resultsFootnote b
de PerioFootnote 23 2014 Acute Yes Weak Medium Extrapolation Study number: Ten observational studies, nine outbreak investigations and a single cross-sectional study, provide evidence to support delayed diagnosis and initiation of airborne precautions among active TB cases can lead to TB transmission in healthcare settings. In many of the reported investigations, at least one active TB infection among investigated contacts was linked to an index patient with a missed or delayed diagnosis by common epidemiology or infection strain. The cross-sectional study by Uppal et al., reports atypical presentation of TB infections and delays in TB diagnosis as the root causes of many TB exposures identified in a single healthcare facility.
Study quality: Across studies, quality was variable, from low to medium.
Consistency of results: The majority of studies were from acute care settings, but exposure events, contact investigations and findings were variable. All of the included studies identified delays in diagnosis and initiation of airborne precautions as infection prevention and control gaps linked to exposure event.
Directness: These studies provide direct evidence to confirm TB transmission in healthcare settings due to gaps in infection prevention and control measures linked to exposure events, particularly delays in diagnosis and prompt initiation of airborne precautions.
Generalizability: Overall, this evidence is generalizable to Canadian hospital and long-term care settings.
Strength of body of evidence: Moderate
Grisaru-SoenFootnote 14 2014 Acute Yes Weak Low Direct
HoldenFootnote 18 2018 Acute Yes Weak Low Direct
JonssonFootnote 24 2013 Acute Yes Weak Medium Direct
KanFootnote 40 2013 Acute Yes N/A N/A Extrapolation
KhatamiFootnote 34 2017 Acute No Weak Low Direct
MedranoFootnote 12 2014 Acute Yes Weak Medium Direct
TownesFootnote 41 2016 Outpatient No Weak Low Direct
UppalFootnote 20 2014 Acute No Weak Medium Direct
HarrisFootnote 22 2013 LTC Yes Weak Low Direct
Overall - - Weak Medium Direct

Abbreviations:
LTC, long-term care; N/A = not applicable

Footnotes:

Footnote a

This body of evidence informs Chapter 14 recommendations and good practice statements on identifying individuals with respiratory TB in the healthcare settings.

Return to footnote a referrer

Footnote b

Rating the quality of the overall body of available evidence for specific recommendations was conducted using the Public Health Agency of Canada Critical Appraisal Toolkit (CAT). Moralejo D, Ogunremi T, Dunn K. Critical Appraisal Toolkit (CAT) for assessing multiple types of evidence. Can Commun Dis Rep. 2017;43(9):176-81. https://doi.org/10.14745/ccdr.v43i09a02

Return to footnote b referrer

Table 2d. Tuberculosis (TB) exposures due to premature discontinuation of airborne precautions
Research question: Have premature discontinuation of airborne precautions in patients or residents been linked to TB exposures in healthcare or long-term care facilities?Footnote a
Study Setting Transmission Study design Quality Directness Critical appraisal resultsFootnote b
HoldenFootnote 18 2018 Acute Yes Weak Low Extrapolation Study number: Three epidemiological investigations report premature discontinuation of airborne precautions linked to exposure.
Study quality: Study quality between the two studies reporting primary evidence was low to medium.
Consistency of results: Both studies report premature discontinuation of airborne precautions. In one instance, airborne precautions were discontinued before sputum analysis. In the other, airborne precautions were removed from a still-infectious patient who completed 14 days of effective therapy but remained symptomatic.
Directness: One study provides direct evidence of missing smear negative sputum. The other study provides extrapolated evidence that suggests sputum smear positivity was not considered when airborne precautions were removed, as the only consideration for discontinuation was completion of treatment.
Generalizability: Overall, this evidence is generalizable to Canadian hospital and long-term care settings.
Strength of body of evidence: Weak
JonssonFootnote 24 2013 Acute Yes Weak Medium Direct
KanFootnote 40 2013 Acute Yes N/A N/A Extrapolation
Overall - - Weak Low Extrapolation

Abbreviations:
N/A = not applicable

Footnotes:

Footnote a

This body of evidence informs Chapter 14 recommendations on identifying individuals with respiratory TB in the healthcare setting.

Return to footnote a referrer

Footnote b

Rating the quality of the overall body of available evidence for specific recommendations was conducted using the Public Health Agency of Canada Critical Appraisal Toolkit (CAT). Moralejo D, Ogunremi T, Dunn K. Critical Appraisal Toolkit (CAT) for assessing multiple types of evidence. Can Commun Dis Rep. 2017;43(9):176-81. https://doi.org/10.14745/ccdr.v43i09a02

Return to footnote b referrer

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Okada RC, Barry PM, Skarbinski J, Chitnis AS. Epidemiology, detection, and management of tuberculosis among end-stage renal disease patients. Infect Control Hosp Epidemiol. 2018;39(11):1367–1374. doi:10.1017/ice.2018.219.

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