Mycobacterium avium complex: Difference between revisions
From IDWiki
Mycobacterium avium complex
No edit summary |
No edit summary |
||
Line 16: | Line 16: | ||
** Natural water, indoor water, pools, hot tubs |
** Natural water, indoor water, pools, hot tubs |
||
* Risk factors |
* Risk factors |
||
− | ** Pulmonary disease: COPD, |
+ | ** Pulmonary disease: [[COPD]], prior [[pneumonia]], prior [[TB]], [[Corticosteroids|steroid]] use, [[silicosis]], [[scoliosis]], [[pectus excavatum]] |
− | ** Disseminated disease: HIV, interferon-gamma defects |
+ | ** Disseminated disease: [[HIV]], interferon-gamma defects |
− | ** Cervical lymphadenitis: children 1-5 years old, HIV with IRIS |
+ | ** [[Cervical lymphadenitis]]: children 1-5 years old, [[HIV]] with [[IRIS]] |
=== Pathophysiology === |
=== Pathophysiology === |
||
* In pulmonary disease, likely inhalation ± microaspiration |
* In pulmonary disease, likely inhalation ± microaspiration |
||
− | * In disseminated disease in AIDS, likely GI colonization then replication and dissemination |
+ | * In disseminated disease in [[AIDS]], likely GI colonization then replication and dissemination |
== Clinical Manifestations == |
== Clinical Manifestations == |
Revision as of 16:30, 13 July 2022
Background
Microbiology
- A slow-growing non-tuberculous mycobacterium
- Comprises M. avium (subspecies hominissuis in humans) and M. intracellulaire
- 28 serovars between the two
- Can colonize airways and GI tract as well as causing disease
Differential Diagnosis
- Pulmonary disease
- M. kansasii
- M. abscessus
Epidemiology
- Common in the environment, likely acquired by inhalation or ingestion (not person-to-person)
- Water, soil, and animals
- Natural water, indoor water, pools, hot tubs
- Risk factors
Pathophysiology
- In pulmonary disease, likely inhalation ± microaspiration
- In disseminated disease in AIDS, likely GI colonization then replication and dissemination
Clinical Manifestations
Pulmonary disease
- Incubation period months to years
- Typically presents with non-specific subacute to chronic respiratory syndrome
- Productive cough, weight loss, fevers, night sweats
- CXR often shows upper-lobe infiltrates ± cavitations ± pleural thickening
- Bronchiectasis on CT in 94%
- Mortality is 15% within 2 to 10 years
- Specific populations/presentations:
- Smokers/COPD/alcohol: typical presentation as above
- Lady Windermere syndrome: slower progression
- Hot tub lung disease: a hypersensitivity pneumonitis associated with inhalation
Disseminated disease
- Almost exclusive to HIV patients with CD4 <100
- Median CD4 was 13
- Typically presents with high fevers, weight loss, night sweats, anemia
- Also abdo pain, diarrhea, intraabdo lymphadenopathy, hepatosplenomegaly, and elevated ALP
- Organ-specific involvement: spleen, lymph nodes, liver, adrenals, stomach, CNS
- Often not lung involvement
- Mortality 50% at 4 months
Cervical lymphadenitis
- Disease of children, usually <3 (80% aged 1 to 5 years)
- Presents as painless unilateral lymph node enlargement
- 10% bilateral
Investigations
Pulmonary disease
- (1) chest radiograph or, in the absence of cavitation, chest high-resolution computed tomography (HRCT) scan
- (2) three or more sputum specimens for acid-fast bacilli (AFB) analysis
- (3) exclusion of other disorders, such as tuberculosis
Diagnosis
Pulmonary disease
- Diagnosis based on presence of both clinical and microbiological evidence
- Clinical:
- Pulmonary symptoms, nodular or cavitary opacities on chest radiograph, or an HRCT scan that shows multifocal bronchiectasis with multiple small nodules; and
- Appropriate exclusion of other diagnoses.
- Microbiological:
- Positive cultures from at least two separate expectorated sputum samples; or
- Positive culture from at least one bronchial wash or lavage; or
- Transbronchial or other lung biopsy with mycobacterial histopathologic features, and either positive culture for NTM or one or more sputum or BALs positive for NTM
Disseminated disease
- Diagnosis based on MAC in culture of sterile site
Management
Pulmonary disease
- Nodular/bronchiectatic disease:
- Clarithromycin (1,000 mg) or azithromycin (500 mg)
- Rifampin (600 mg)
- Ethambutol (25 mg/kg)
- Three times weekly (because daily never tolerated)
- If fibrocavitary MAC lung disease or severe nodular/bronchiectatic disease:
- Clarithromycin (500–1,000 mg) or azithromycin (250 mg) daily
- Rifampin (600 mg) or rifabutin (150–300 mg) daily
- Ethambutol (15 mg/kg) daily
- And consider adding three-times-weekly amikacin or streptomycin early in therapy
- Duration is until culture negative on therapy for at least 1 year
- Refer to Ophthalmology for monitoring while on ethambutol
Disseminated disease
- Antibiotics
- Clarithromycin (1,000 mg/d) or azithromycin (250 mg/d)
- Ethambutol (15 mg/kg/d)
- ± rifabutin (150–350 mg/d)
- Duration is until resolution of symptoms and reconstitution of cell-mediated immune function (e.g. CD4 >100)
Prophylaxis
- Indicated for adults with (AIDS) with CD4 <50; but not done and no longer in the HIV guidelines
- Antibiotics: azithromycin 1,200 mg/week or clarithromycin 1,000 mg/day
- Second-line: rifabutin 300 mg/day (less well tolerated)