METHODS: The Connecticut Department of Public Health (CDPH) requested that all providers obtain INH-RPT for the treatment of LTBI from CDPH, free-of-charge. To monitor completion of treatment, adverse drug effects, and feasibility of using INH-RPT in Connecticut, active surveillance is done for all INH-RPT prescriptions and DOT logs are requested for each patient. These data were analyzed for the period March 2012, when the regimen was implemented, through December 31st, 2012.
RESULTS: Fifty-six patients started treatment for LTBI using 12 doses of INH-RPT. The median age was 37 years (range: 14 – 90); 29 (52%) were male. Among patients with known data, 11/49 (22%) were non-Hispanic black, 10/49 (20%) were non-Hispanic white, and 10/49 (20%) were Asian; 18/49 (37%) were Hispanic. Country of origin was known for 51 patients; 34 (67%) were foreign born.
Of 56 patients, 26 (46%) are currently receiving treatment or have planned start dates. Among the remaining 30 patients, 25 (83%) completed treatment and 5 (17%) stopped treatment. Four patients stopped because of nausea, diarrhea, rash, or increased serum transaminase concentrations. One patient stopped because of an event unrelated to treatment.
CONCLUSIONS: Based on tolerability, safety and treatment completion, the early stages of implementing weekly 12-dose INH-RPT for the treatment of LTBI in Connecticut suggest the regimen is a promising alternative to 9 months of daily INH.