HTB

CDC study shows rifampin/pyrazinamide therapy can cause severe liver damage

Graham McKerrow, HIV i-Base

Treatment of latent TB with a two-month therapy regimen of rifampin and pyrazinamide (RZ) can cause severe liver damage and even death, according to a study by the US Centers for Disease Control and Prevention (CDC).

The CDC has previously reported surveillance data of severe liver damage in patients treated with a daily and twice-weekly two-month regimen of RZ. To estimate the incidence of severe liver damage they collected data on patients in the United States who received treatment between January 2000 and June 2002. [1] CDC found reports of 48 latent TB patients with confirmed cases of severe liver injury after receiving the treatment. Eleven patients died. As a result the American Thoracic Society and CDC now recommend that this regimen should not normally be offered to people with latent TB.

The agency recommends a nine-month regimen of isoniazid as the preferred treatment for latent TB. [2] It also says that rifampin and pyrazinamide should continue to be used in multidrug regimens for the treatment of active TB disease.

Ref: Centers for Disease Control and Prevention (CDC); American Thoracic Society. Update: adverse event data and revised American Thoracic Society/CDC recommendations against the use of rifampin and pyrazinamide for treatment of latent tuberculosis infection – United States, 2003. MMWR Morb Mortal Wkly Rep. 2003 Aug 8;52(31):735-9.

CDC summary:
http://www.cdc.gov/nchstp/tb/pubs/tbfactsheets/250110.htm

References:

  1. DC. Update: Fatal and severe liver injuries associated with rifampin and pyrazinamide for latent tuberculosis infection, and revisions in American Thoracic Society/CDC recommendations – United States, 2001. MMWR 2001;50 (No.34).
    http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5034a1.htm
  2. 2. CDC. Update: Adverse Event Data and Revised American Thoracic Society/CDC Recommendations Against the Use of Rifampin and Pyrazinamide for Treatment of Latent Tuberculosis Infection. MMWR 2003; 52 (No. 31).
    http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5231a4.htm

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