Current guidelines recommend the treatment of latent tuberculosis infection (LTBI) among liver transplantation (LT) candidates with compensated cirrhosis, with isoniazid plus pyridoxine as the preferred regimen. (1)(2)(3) Nevertheless, completion rates and tolerability are low. Fluoroquinolones (FQs) exhibit good antimycobacterial activity and a favorable safety profile and could serve as an alternative to isoniazid. To provide further insight into the role of FQs for this indication, we report our experience with a 9-month moxifloxacin regimen for the treatment of LTBI in the LT setting.
Patients and MethodsSince November 2015, the use of moxifloxacin (400 mg daily) for 9 months, preferably implemented while patients are on the waiting list, has replaced isoniazid or rifampicin for the treatment of LTBI in LT candidates and recipients in our center. If pretransplant treatment was not feasible, moxifloxacin was initiated once graft function was normalized. The study was primarily aimed at evaluating the safety and tolerability of the 9-month moxifloxacin regimen, whereas the occurrence of active tuberculosis (TB) upon completion of LTBI therapy was analyzed as the secondary outcome. Details on institutional protocols, definitions, patient follow-up, and statistical methods are available as Supporting Information.
ResultsOverall, 38 patients (28 LT candidates and 10 LT recipients) received moxifloxacin for LTBI between December 2015 and November 2019 (Supporting Table 1). A total of 2 patients with no history of liver disease had previously developed isoniazid-induced acute liver failure while on LTBI therapy.The median duration of moxifloxacin treatment was 260 days (interquartile range [IQR], 180-274). Of 28 candidates, 17 (60.7%) underwent transplantation while on LTBI therapy at a median interval of 103 days (IQR, 53-167) from the initiation of moxifloxacin.