Table 2.
Duration | Intensive phase | Continuous phase | ||
---|---|---|---|---|
Method A | Standard | 6 months* | RFP+NH+PZA+SM (or EB) for 2 months |
RFP+INH for 4 months*,** |
Method B | Only when PZA cannot be administered *** |
9 months * | RFP+INH+SM (or EB) for 2 months |
RFP+INH for 7 months*,** |
INH: isoniazid, RFP: rifampicin, PZA: pyrazinamide, EB: ethambutol, SM: streptomycin
* The treatment period of continuous phase can be prolonged by 3 months for patients with severe lesions or those with diabetes etc, resulting in 9 months for Method A and 12 months for Method B, in total.
** When drug susceptibility is unknown and symptom improvement is unclear, SM (or EB) is continued until drug susceptibility is identified or clinical improvement is confirmed.
*** Method B is used only when pyrazinamide cannot be administered due to adverse reactions for those such as patients with underlying hepatic disorders or elderly patients aged 80 years or older.