Clinical Manual for Management of the HIV-Infected ... - myCME.com
Clinical Manual for Management of the HIV-Infected ... - myCME.com
Clinical Manual for Management of the HIV-Infected ... - myCME.com
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Section 6—Disease-Specific Treatment | 6–75<br />
Tuberculosis Treatment in Resource-Limited Settings<br />
Background<br />
Tuberculosis (TB) is <strong>the</strong> most <strong>com</strong>mon severe<br />
opportunistic infection associated with <strong>HIV</strong> in many<br />
resource-limited areas such as sub-Saharan Africa.<br />
The enormous and increasing number <strong>of</strong> cases <strong>of</strong> TB<br />
associated with <strong>HIV</strong> infection has greatly increased<br />
<strong>the</strong> demands on TB treatment programs. TB treatment<br />
in <strong>HIV</strong>-infected patients is different in resourcelimited<br />
settings than in resource-abundant settings,<br />
and treatment details may differ by country. In general,<br />
<strong>the</strong> emphasis <strong>of</strong> TB treatment and control in resourcelimited<br />
areas has been on diagnosing sputum smearpositive<br />
patients (ie, those with infectious pulmonary<br />
TB) to minimize <strong>the</strong> need <strong>for</strong> expensive technology<br />
and to maximize <strong>the</strong> public health impact <strong>of</strong> treatment.<br />
The target <strong>for</strong> many national TB control programs is<br />
to diagnose 70% <strong>of</strong> new cases, and <strong>for</strong> 85% <strong>of</strong> newly<br />
diagnosed patients to <strong>com</strong>plete a course <strong>of</strong> <strong>the</strong>rapy. The<br />
following re<strong>com</strong>mendations <strong>for</strong> diagnosis and treatment<br />
are derived from guidelines by <strong>the</strong> World Health<br />
Organization (WHO) and <strong>the</strong> International Union<br />
Against Tuberculosis and Lung Disease.<br />
See <strong>the</strong> Treatment <strong>of</strong> Latent Tuberculosis in Resource-<br />
Limited Settings chapter <strong>for</strong> a discussion <strong>of</strong> isoniazid<br />
preventive treatment (IPT) <strong>for</strong> <strong>HIV</strong>-infected persons.<br />
For more in<strong>for</strong>mation on tuberculosis, including<br />
diagnosis and treatment, see chapter Mycobacterium<br />
tuberculosis: Treatment in <strong>the</strong> United States and O<strong>the</strong>r<br />
High-In<strong>com</strong>e Nations.<br />
Diagnosis<br />
<strong>HIV</strong> counseling and voluntary testing should be<br />
encouraged <strong>for</strong> every person diagnosed with TB. In<br />
addition, screening <strong>for</strong> TB symptoms should occur at<br />
every health care interaction with <strong>HIV</strong>-infected persons.<br />
Patients with both conditions should be referred<br />
between <strong>the</strong> TB and <strong>HIV</strong> treatment facilities in order<br />
to access both treatments appropriately. Coordination<br />
between TB and <strong>HIV</strong> treatment is crucial because <strong>of</strong><br />
potential drug interactions, increased risk <strong>of</strong> toxicity,<br />
risk <strong>of</strong> immune reconstitution inflammatory syndrome<br />
(IRS), and increased adherence challenges. In many<br />
countries, an ef<strong>for</strong>t to coordinate <strong>HIV</strong> and TB care is<br />
just beginning.<br />
Three sputum smears should be examined <strong>for</strong> acid-<br />
fast bacilli (AFB) in all patients with chronic cough.<br />
The presence <strong>of</strong> o<strong>the</strong>r respiratory symptoms (eg,<br />
breathlessness, chest pain, hemoptysis) or systemic<br />
symptoms (eg, fever, night sweats, weight loss, loss <strong>of</strong><br />
appetite) increase <strong>the</strong> likelihood <strong>of</strong> pulmonary TB. For<br />
outpatients, an initial (spot) sputum specimen should<br />
be obtained on <strong>the</strong> day a patient presents <strong>for</strong> evaluation.<br />
The patient <strong>the</strong>n is sent home with a sputum cup to<br />
collect a sample immediately after awakening <strong>the</strong> next<br />
morning. The patient brings <strong>the</strong> morning specimen<br />
back to <strong>the</strong> health facility <strong>the</strong> day it is collected. On<br />
that day, <strong>the</strong> patient provides a second spot specimen in<br />
<strong>the</strong> health facility, so that 3 specimens are collected in 2<br />
days. All 3 are stained and examined microscopically <strong>for</strong><br />
AFB.<br />
<strong>HIV</strong>-infected patients with TB, especially those with<br />
advanced immunosuppression, <strong>of</strong>ten have ei<strong>the</strong>r smearnegative<br />
pulmonary disease or extrapulmonary disease.<br />
In such cases, diagnosis relies on clinical judgment and<br />
radiographic imaging, and sometimes on aspirates and<br />
biopsies. In some locations, x-rays may be unavailable,<br />
so TB treatment may be instituted in smear-negative<br />
patients in whom pulmonary TB is suspected (eg,<br />
in patients in whom at least 1 trial <strong>of</strong> standard<br />
antibiotics has been ineffective and a medical doctor<br />
or an appropriately trained clinician has not made an<br />
alternative diagnosis). In some cases, diagnostic testing<br />
may not be available, and AIDS patients with a wasting<br />
febrile disease may be treated empirically <strong>for</strong> TB.<br />
TB lymphadenitis <strong>of</strong>ten can be diagnosed on an<br />
AFB smear <strong>of</strong> a needle aspirate <strong>of</strong> a suspicious<br />
lymph node, or on <strong>the</strong> gross appearance <strong>of</strong> caseous<br />
necrosis in a biopsied lymph node. AFB smears are<br />
usually negative in pleural, pericardial, peritoneal,<br />
joint, and cerebrospinal fluids <strong>of</strong> patients with TB in<br />
those <strong>com</strong>partments. Diagnosis is based on clinical<br />
presentation and on cell counts and chemistry tests <strong>of</strong><br />
<strong>the</strong> fluids. (Where chemistry tests are not available, <strong>the</strong><br />
fluid may be observed <strong>for</strong> <strong>for</strong>mation <strong>of</strong> protein clots<br />
over <strong>the</strong> course <strong>of</strong> several hours, indicating elevated<br />
fluid protein levels.) Liver and bone marrow biopsy may<br />
be helpful in diagnosing disseminated TB, revealing<br />
granulomas if not acid-fast organisms. If possible,<br />
<strong>the</strong>se fluids and biopsied tissues should be cultured <strong>for</strong><br />
Mycobacterium tuberculosis.