Abstract

BackgroundWhile prednisolone is commonly used to treat recent nerve function impairment (NFI) in leprosy patients, the optimal treatment duration has not yet been established. In this “Treatment of Early Neuropathy in Leprosy” (TENLEP) trial, we evaluated whether a 32-week prednisolone course is more effective than a 20-week course in restoring and improving nerve function.MethodsIn this multi-centre, triple-blind, randomized controlled trial, leprosy patients who had recently developed clinical NFI (<6 months) were allocated to a prednisolone treatment regimen of either 20 weeks or 32 weeks. Prednisolone was started at either 45 or 60 mg/day, depending on the patient’s body weight, and was then tapered. Throughout follow up, NFI was assessed by voluntary muscle testing and monofilament testing. The primary outcome was the proportion of patients with improved or restored nerve function at week 78. As secondary outcomes, we analysed improvements between baseline and week 78 on the Reaction Severity Scale, the SALSA Scale and the Participation Scale. Serious Adverse Events and the need for additional prednisolone treatment were monitored and reported.ResultsWe included 868 patients in the study, 429 in the 20-week arm and 439 in the 32-week arm. At 78 weeks, the proportion of patients with improved or restored nerve function did not differ significantly between the groups: 78.1% in the 20-week arm and 77.5% in the 32-week arm (p = 0.821). Nor were there any differences in secondary outcomes, except for a significant higher proportion of Serious Adverse Events in the longer treatment arm.ConclusionIn our study, a 20-week course of prednisolone was as effective as a 32-week course in improving and restoring recent clinical NFI in leprosy patients. Twenty weeks is therefore the preferred initial treatment duration for leprosy neuropathy, after which likely only a minority of patients require further individualized treatment.

Highlights

  • Leprosy is an infectious disease caused by Mycobacterium leprae

  • A 20-week course of prednisolone was as effective as a 32-week course in improving and restoring recent clinical nerve function impairment (NFI) in leprosy patients

  • NFI can develop before multidrug treatment (MDT) has started, but it can arise during MDT and even several years after leprosy treatment has been completed [2,3]

Read more

Summary

Introduction

Leprosy is an infectious disease caused by Mycobacterium leprae. Since the introduction of antibiotic multidrug treatment (MDT) in the 1980’s, the number of leprosy diagnoses has decreased dramatically, and the disease was even declared eliminated as a public health problem at a global level in the year 2000 –i.e. less than 1 case per 10 000 inhabitants. A main complication of leprosy is neuropathy, which often causes sensory and motor nerve function impairment (NFI). NFI can develop before MDT has started, but it can arise during MDT and even several years after leprosy treatment has been completed [2,3]. While prednisolone is commonly used to treat recent nerve function impairment (NFI) in leprosy patients, the optimal treatment duration has not yet been established. In this “Treatment of Early Neuropathy in Leprosy” (TENLEP) trial, we evaluated whether a 32-week prednisolone course is more effective than a 20-week course in restoring and improving nerve function

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call