TIMING OF SPUTUM EXAMINATION
|
AIM
|
ACTION
|
COMMENTS
|
END OF INTENSIVE PHASE
|
One week before the end of the two months’ intensive phase of treatment (at seven weeks)
|
To determine smear conversion a sign of good
clinical progress
|
(1) | If negative, change to the continuation phase of treatment at the end of the 8th week of intensive phase treatment. |
|
This means the patient is responding well to treatment. Educate and counsel patient about importance of treatment compliance.
|
(2) | Register the patient as "negative". |
|
To guide the health worker on whether to change the patient to continuation phase of treatment or extend the intensive phase.
|
(3) | If positive, check for treatment compliance, re-assess patient clinically: |
(a) | Conduct LPA (or culture and DST, if LPA is not available). |
(b) | Continue with the intensive phase treatment for one month. |
(c) | Register the patient as "positive". |
(d) | Review the drug susceptibility results when available. |
|
This indicates the following:
• | That the initial phase of therapy was poorly supervised and that patient’s compliance to treatment was poor. |
• | That there is a slow rate of progress with smear conversion, which is common in patients with extensive cavitations and a high bacillary load at diagnosis. |
• | That the patient may have resistance to the other TB drugs i.e. Isoniazid (since only Rifampicin resistance was excluded upfront) or may have been reinfected with a drug resistant strain. |
• | The patient could have non-tuberculous mycobacterial infection. |
• | The patient may have another condition or taking other medication that affects the absorption or effectiveness of the TB drugs. |
• | Patient may have been infected with mixed strains with amplification of resistant strains due to treatment. |
Address treatment compliance by counselling the patient and identifying a treatment supporter where necessary.
|
FOR THOSE REMAINING POSITIVE AT 2 MONTHS
|
Repeat smear one
week before the
end of the third
month (11 weeks)
|
|
(4) | If negative and drug susceptible, change to continuation phase of treatment at the end of the 12th week. Register the patient as "negative". |
(5) | If negative and Isoniazid mono resistant TB is confirmed, continue intensive phase treatment and refer patient to MDRTB for assessment and registration in DR-TB register. Register the patient as "Isoniazid mono-resistant TB" in the TB register. |
(6) | If still positive and RRTB or MDR-TB is confirmed, stop treatment and refer patient to the MDR-TB treatment initiation site for assessment and treatment initiation. Register the patient as "RR-TB or MDR-TB" in TB register. |
|
The intensive phase treatment is not extended beyond three months in patients with drug susceptible TB.
|
END OF CONTINUATION PHASE
|
One week before the end of the four months’ continuation phase (at 23 weeks)
|
To determine the final outcome of treatment for the patient.
|
(1) | If negative, stop treatment at the end of the 24th week of treatment. Register the patient as "cured". |
|
Educate the patient about TB prevention and healthy lifestyle.
|
(2) | If positive, stop TB treatment. Register patient as "treatment failure". |
(a) | Conduct LPA and DST for pyrazinamide and ethambutol. |
(b) | Review the results when available. |
|
This indicates the following:
• | That the patient was reinfected with a sensitive or resistant strain. |
• | The treatment during the continuation phase was unsupervised and patient compliance was poor. |
|
FOR THOSE REMAINING POSITIVE AT 6 MONTHS
|
|
To determine further management of the patient.
|
(1) | If drug susceptible, restart TB treatment, counsel the patient and provide treatment support. |
|
|
|
|
(2) | If DR-TB RR-TB, Isoniazid Mono resistant, MDR-TB, Other resistance), refer to the MDR-TB treatment initiation site hospital for assessment and treatment. |
|
|