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Canada Communicable Disease Report
Volume 28 • ACS-7
15 December 2002
An Advisory Committee Statement (ACS)
The Canadian Tuberculosis Committee*†
RECOMMENDATIONS FOR THE SCREENING AND PREVENTION OF
TUBERCULOSIS IN PATIENTS WITH HIV AND THE SCREENING FOR HIV IN TUBERCULOSIS
PATIENTS AND THEIR CONTACTS
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Preamble
The Canadian Tuberculosis Committee (CTC) provides Health Canada with
ongoing, timely and scientifically based advice on national strategies
and priorities with respect to tuberculosis prevention and control in
Canada. Health Canada acknowledges that the advice and recommendations
set out in this statement are based upon the best current available scientific
knowledge and medical practice.
It is disseminating this document for information purposes to the medical
community involved in the care of individuals with tuberculosis and/or
HIV/AIDS.
Screening and Prevention of Tuberculosis in Patients with HIV
The HIV epidemic has had a dramatic impact on tuberculosis (TB) rates
and tuberculosis control in populations in which both infections are prevalent(1).
HIV, in particular advanced HIV (AIDS), is the most potent risk factor
ever identified for the progression to disease of recent or remotely acquired
infection with Mycobacterium tuberculosis(2). It operates
by destroying the two types of immune cell most important to the containment
of tubercle bacilli (macrophages and CD4 receptor bearing lymphocytes)(3).
Among people infected with M. tuberculosis who are not receiving
highly active antiretroviral therapy (HAART), the estimated risk of active
tuberculosis relative to patients with no known risk factor is 170.0 for
AIDS and 113.0 for HIV infection without AIDS(2). Cases of
TB thus produced increase the risk of transmission of M. tuberculosis
within the community, thereby constituting a second, indirect mechanism
by which HIV increases TB morbidity(4).
In Canada, dormant or latent tuberculosis infection (LTBI) is most commonly
found in four groups: those born in countries where TB is endemic, Aboriginal
people, the inner city poor and homeless, and elderly people(5).
Co-infection with HIV is not uncommon among inner city people with a history
of injection drug use(6).
Recent data suggest that the incidence of HIV/AIDS is increasing among
Aboriginal people(6-8) and those born in tuberculosis endemic
countries(9). Treatment of LTBI has been shown to reduce the
risk of progression to active disease in HIV-TB co-infected individuals(10,11).
The following recommendations are made:
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Every patient with newly diagnosed HIV infection should be assessed
for the presence of active TB at the time of diagnosis of HIV. An
inquiry about symptoms that would suggest active TB (cough, especially
if productive or associated with hemoptysis, fever, night sweats,
weight loss) should be made and any history of TB or known/likely
exposure to it ascertained. For patients who report that they have
received treatment of active TB or LTBI in the past, the adequacy
of that treatment must be assessed. As well, a physical examination
that includes examination of extrapulmonary sites of disease, such
as lymph nodes(12), and chest radiography should be performed,
and features of current or past TB sought. The examiner should be
aware that the clinical presentation of TB may be altered in the presence
of HIV infection and that radiographic features may be altered or
absent in approximate proportion to the individual's degree of
immunosuppression(3). People with suspected active TB should
have sputum or other appropriate specimens submitted for acid-fast
bacilli (AFB) smear and culture.
-
Health care workers caring for patients with HIV infection should
maintain a high level of suspicion for TB.
-
Except in those with a history of active TB or a well documented
previous, positive tuberculin skin test (TST), every HIV-infected
person should be given a TST with intermediate strength (5-TU) purified
protein derivative by the Mantoux method, which should be read 48
to 72 hours later by a health care worker experienced in reading TSTs.
-
TB screening with TST should be performed as soon as possible after
HIV infection is diagnosed, because the reliability of the TST can
diminish as the CD4 lymphocyte count declines.
-
For those in whom annual testing is felt to be justified by high
infection rates, a baseline two step TST should be considered(2).
-
Induration of >= 5 mm on the TST should be considered indicative
of TB infection(2,3).
-
Routine anergy testing is not recommended(13,14). Administration
of TB preventive therapy to anergic, HIV-infected individuals has
not been found to be useful or cost-effective if none of the other
indications is present (see below)(15-17).
-
TST negative patients with evidence of old, healed TB on the chest
radiograph, especially those with a history of TB exposure, should
be considered for TB preventive therapy once active tuberculosis has
been excluded. Repeat TST may be considered after institution of antiretroviral
therapy and evidence of immune reconstitution(3).
-
Unless specifically contraindicated, HIV-positive patients who a)
have a positive TST ( >= 5 mm of induration), b) have not already
been treated for TB infection, and c) have test results excluding
active TB should be strongly encouraged to take preventive therapy(1,18-20).
This preventive therapy is indicated even if the date of TST conversion
cannot be determined. Because of the very high risk of development
of active TB in HIV-TB co-infected individuals, creative means of
enhancing adherence, such as directly observed preventive therapy,
should be considered, particularly if there are concerns about the
patient's adherence. Preventive therapy regimens and monitoring
are outlined in the 5th edition of the Canadian Tuberculosis Standards,
Web site: www.lung.ca/tb/TBStandards_Eng.pdf
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HIV-infected close contacts of patients with infectious TB should
receive treatment for presumptive LTBI, even when repeat TST after
contact is not indicative of latent infection(20). Because
re-infection can occur, this may, at times, imply re-treatment of
a person who has already undergone treatment in the past.
-
Preventive therapy is recommended during pregnancy for HIV- infected
patients who have either a positive TST or a recent history of exposure
to active TB, after active tuberculosis has been excluded.
-
HIV-infected people who are candidates for, but who do not receive,
TB preventive therapy should be assessed periodically for symptoms
of active TB as part of their ongoing management of HIV infection.
Clinicians should educate them about the symptoms of TB and advise
them to seek medical attention promptly should such symptoms develop.
-
The administration of BCG vaccine to HIV-infected patients is contraindicated
because of its potential to cause disseminated disease.
-
HIV-infected patients should be advised that certain activities
and occupations may increase the likelihood of exposure to TB. These
include volunteer work or employment in health care facilities, correctional
institutions, and shelters for the homeless, as well as travel to
TB endemic countries.
TB disease in an HIV-infected person is an AIDS defining illness. Both
TB and AIDS should be reported to the Public Health Department(21).
Screening for HIV in TB Patients and Their Contacts
Patients with TB constitute an important “sentinel“ population
for HIV screening. In some African countries with high TB prevalence,
HIV prevalence exceeds 50% among TB patients(22). Between 1985
and 1992, TB patients in the United States were 204-fold more likely
to have AIDS than the general population(23). The benefits
of identifying previously unrecognized HIV infection are substantial in
terms of both the opportunities for preventing future HIV transmission
and the large potential benefits to the patient of antiretroviral therapy(3).
Knowledge of the HIV serostatus of TB patients may also influence the
treatment of their TB(17). Even in those not receiving antiretroviral
drugs there may be an increased risk of adverse reactions from antituberculosis
drugs(24). Because HIV-infected people are at risk of peripheral
neuropathy, co-administration of pyridoxine with isoniazid may be prudent.
For some HIV-infected TB patients malabsorption of their anti-
tuberculosis drugs has been reported, so that measurement of serum drug
levels may be necessary if there is a poor response to treatment(3).
The following recommendations are made:
-
All patients with newly diagnosed TB should be strongly encouraged
to undergo HIV serologic testing according to established guidelines(25,26).
-
HIV-testing of contacts of infectious TB cases should be considered
if they are at risk for HIV(27,28).
-
Additional information resources concerning HIV should be available
to patients for whom HIV testing is recommended as well as to other
patients seen by TB programs.
Health care providers, administrators, and TB controllers should strive
to promote coordinated care for patients with TB and HIV, and to improve
information sharing between TB control programs and HIV/AIDS programs.
Acknowledgements
The authors would like to thank members of the Centre for Infectious
Disease Prevention and Control, Public Health Agency of Canada, Health
Canada, the Canadian Thoracic Society, and the Canadian Infectious Disease
Society for their critical review and ultimate approval of these recommendations.
They would also like to thank Susan Falconer for her secretarial assistance.
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* Members: Dr. V. Hoeppner (Chair); Dr. M Baikie; Dr. C Balram;
Ms. P. Bleackley; Ms. C. Case; Dr. E. Ellis (Executive Secretary); R.K.
Elwood (Past Chair); Ms. P. Gaba;, Dr. B. Graham; Dr. B. Gushulak; Ms.
C. Helmsley; Dr. E.S. Hershfield; Ms. R. Hickey; Dr. A. Kabani; Dr. B.
Kawa; Dr. R. Long; Dr. F. Stratton; Ms. N. Sutton; Dr. L. Sweet; Dr. T.N.
Tannenbaum.
† This statement was prepared by Dr. R. Long, Dr. S. Houston, and
Dr. E.S. Hershfield. It has been approved by the Canadian Tuberculosis
Committee, Canadian Thoracic Society of the Canadian Lung Association,
Canadian Infectious Disease Society, and Centre for Infectious Disease
Prevention and Control, Public Health Agency of Canada, Health Canada.
[Canada Communicable
Disease Report]
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