Mycobacterium tuberculosis: Difference between revisions

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Mycobacterium tuberculosis
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==== Liver Disease ====
 
==== Liver Disease ====
   
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* Most of the first-line medications (except [[ethambutol]]) can cause drug-induced hepatotoxicity and should be avoided
* rifa
 
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**[[Rifampin]] may be considered in more extensive disease
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*In general, a combination of [[fluoroquinolone]] plus [[ethambutol]] plus an injectable such as [[amikacin]] for the first 2 months, followed by [[fluoroquinolone]] and [[ethambutol]] alone to complete 18 months total
   
 
==Prevention==
 
==Prevention==

Revision as of 23:03, 3 February 2022

  • Mycobacterium tuberculosis causes tuberculosis
  • Most commonly pulmonary TB but extrapulmonary tuberculosis is possible (including adenitis, gastrointestinal TB, pericarditis, meningitis)
  • Standard treatment for susceptible TB is RIPE x2mo then RI x4mo

Background

Microbiology

  • Fastidious, aerobic acid-fast bacillus
  • Cell wall has high lipid content
  • Generation time is very long (15 to 20 hours)
  • M. tuberculosis is a complex that comprises seven species:
    • M. tuberculosis sensu stricto: most common causative organism worldwide
    • M. africanum: 50% of cases in West africa
    • M. canetti: rare cause in Eastern African
    • M. bovis: disease in cattle but can infect humans
    • M. caprae: disease in cattle
    • M. microti: disease in rodents
    • M. pinnipdeii: disease in seals, with rare human infection

Epidemiology

  • Typically spread via airborne route
    • Droplets are expelled during coughing, sneezing, or talking, and are suspended in the air
    • They can remain for up to 30 minutes
    • Killed by ultraviolet light
    • Not transmitted via fomites
  • About a third of the world is infected, mostly as latent tuberculosis
    • This progresses to active tuberculosis at about 3 or 4% in the first year and 5% over the rest of their life
  • Reinfection accounts for ~40% of active tuberculosis in endemic countries
  • Highest rates in sub-Saharan Africa and south/southeast Asia

Risk Factors

  • Source factors, such as sputum smear positivity, cough, cavitations
  • Exposure duration, closeness of contact
  • Factors in the exposed person, such as immune compromise, HIV status

Clinical Manifestations

Classification

  • Primary vs. reactivation vs. reinfection
  • Latent vs. active

Primary tuberculosis

  • Primary tuberculosis is usually asymptomatic
  • Possible presentations include mild URTI with cough and/or fever
  • May be seen on CXR as infiltrate in mid-lung zones with hilar adenopathy
  • Ghon complex, especially in children
  • May progress in children and the immunocompromised patients
  • Immunological phenomena
    • Erythema nodosum
    • Phlyctenular conjunctivitis
    • Erythema induratum

Pulmonary tuberculosis

Extra-pulmonary tuberculosis

Latent tuberculosis

Other

Investigations

  • Radiography: chest x-ray with or without CT chest
    • Primary TB: consolidation, lymphadenopathy, pleural effusion, Ghon complex
    • Reactivation TB: patchy upper-lobe consolidation, cavitation, fibrosis, pleural disease
    • Miliary TB: uniform 1-3 mm diameter diffuse nodules

Diagnosis

  • Latent tuberculosis testing
    • Tuberculin skin test (TST)
    • Interferon-gamma release assay (IGRA)
  • Serology or immunologic testing
    • Urine lipoarabinomannan antigen
  • Microbiology
    • Samples can include routine or induced sputum (x3) or bronchoscopy, or tissue sample
    • Spontaneous sputum should include at least one morning sputum, ideally, but can be done all in a row at least one hour apart if needed
    • Acid-fast bacillus culture of sputum x3 is about 70% sensitive, and PCR (ANTB) x1 is about 75% sensitive
  • Molecular testing
    • PCR, including GeneXpert

Management

Antibiotics

Drug Dose Side effects
First-line medications
Isoniazid 5 mg/kg daily, max 300 mg daily, with pyridoxine 25 mg po daily Rash, hepatitis, neuropathy, CNS toxicity, anemia
Rifampin 10 mg/kg daily Drug interactions, rash, hepatitis, flu-like illness, neutropenia, thrombocytopenia
Pyrazinamide 25 mg/kg daily, max 2 g daily Hepatitis, rash, arthralgia, gout
Ethambutol 20 mg/kg daily, max 1.2 g daily Optic/retrobulbar neuritis, rash
Second-line medications
Streptomycin 15 mg/kg daily, max 1 g Auditory and vestibular toxicity, renal toxocity, avoid in pregnancy
Amikacin, kanamycin, or capreomycin 15 mg/kg daily, man 1 g
Ethionamide 250 mg BID to TID, max 1 g GI disturbance, hepatotoxicity, endocrine effects, neurotoxicity, avoid in pregnancy
Para-amino salicylic acid 4 g BID or TID, max 10 g GI disturbance, hepatic dysfunction, hypothyroidism, avoid in aspirin allergy
Cycloserine 250 mg BID to TID, max 1 g Avoid in epilepsy, psychiatric illness, and alcoholism
Levofloxacin 500 to 1000 mg po daily GI disturbance, headache, anxiety, tremor, long QT, avoid in pregnancy and children
Moxifloxacin 400 to 600 mg daily
Rifabutin 300 mg daily Hepatotoxicity, uveitis, thrombocytopenia, neutropenia, drug interactions
Clofazimine 100 to 300 mg daily Skin discolouration, conjunctiva, cornea, body fluid discolouration, GI intolerance, photosensitivity
Third-line medications
Linezolid 600 mg po daily
Bedaquiline 400 mg po daily for 2 weeks followed by 200 mg thrice weekly Arthralgias, dizziness, headache, hyperuriemia, insomnia, myalgia, nausea, prolonged ECG QT interval, pruritus, and vomiting
Pretomanid
Delamanid
Adjunctive therapies
Corticosteroids for patients with tuberculous meningitis or tuberculous pericarditis Prednisone 40 to 80 mg po daily for 6 to 12 weeks

Immune Reconstitution Inflammatory Syndrome (IRIS)

Drug-Induced Liver Injury (DILI)

  • Most common complication leading to treatment interruption, with a mortality of 6-12% if drugs are not stopped
  • Pyrazinamide, followed by isoniazid, then rifampin, are the most common causes of liver injury12
  • Most patients can have the same TB drugs reintroduced without recurrence of DILI, though recurrence can be delayed
  • Procedure
    • Hold if ALT >120 and symptoms, if ALT >200 even without symptoms, or bili >2x ULN
    • Switch to second-line meds
    • Reintroduce the original drugs once AST & ALT are <2x ULN
    • Only rechallenge with pyrazinamide if it was a mild case

Adherence to Treatment

Special Populations

Liver Disease

Prevention

Vaccination

  • BCG vaccine given at or shortly after birth in many countries

Infection Prevention and Control

  • All cases of suspected tuberculosis should be placed in airborne isolation until three sputum smears are negative for tuberculosis, unless it is still suspected and no other diagnosis is made
    • Sputum samples minimum of 1 hour apart, and at least one early morning sample
    • Three induced sputa are preferable to one bronchoscopy
    • Can accept a single negative PCR test if patient is low probability
    • Can accept two negative PCR tests or 1 negative PCR and 2 negative smears if patient is high probability
  • For patients with smear-negative, culture-positive, drug-susceptible respiratory TB:
    • Continue airborne precautions until clinical evidence of improvement and a minimum of 2 weeks of effective therapy
    • Can be discharged home provided there is clinical improvement, drug-resistant TB is not suspected, and there is no contraindication for home isolation
  • For patient with smear-positive, culture-positive, drug-susceptible respiratory TB:
    • Continue airborne precautions as above, but additionally require three negative sputum smears to be negative before they are taken out of airborne isolation
    • Can be discharge home as above
  • For patients with rifampin- or multidrug-resistant TB:
    • Continue airborne precautions as above, but additionally require three negative sputum cultures to be negative before they are taken out of airborne isolation

Further Reading

References

  1. ^  Daphne Yee, Chantal Valiquette, Marthe Pelletier, Isabelle Parisien, Isabelle Rocher, Dick Menzies. Incidence of Serious Side Effects from First-Line Antituberculosis Drugs among Patients Treated for Active Tuberculosis. American Journal of Respiratory and Critical Care Medicine. 2003;167(11):1472-1477. doi:10.1164/rccm.200206-626oc.
  2. ^  Jussi J. Saukkonen, David L. Cohn, Robert M. Jasmer, Steven Schenker, John A. Jereb, Charles M. Nolan, Charles A. Peloquin, Fred M. Gordin, David Nunes, Dorothy B. Strader, John Bernardo, Raman Venkataramanan, Timothy R. Sterling. An Official ATS Statement: Hepatotoxicity of Antituberculosis Therapy. American Journal of Respiratory and Critical Care Medicine. 2006;174(8):935-952. doi:10.1164/rccm.200510-1666st.