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Effectiveness of 32 versus 20 weeks of prednisolone in leprosy patients with recent nerve function impairment: A randomized controlled trial.
Wagenaar, Inge; Post, Erik; Brandsma, Wim; Bowers, Bob; Alam, Khorshed; Shetty, Vanaja; Pai, Vivek; Husain, Sajid; Sigit Prakoeswa, Cita Rosita; Astari, Linda; Hagge, Deanna; Shah, Mahesh; Neupane, Kapil; Tamang, Krishna Bahadur; Nicholls, Peter; Richardus, Jan Hendrik.
Afiliação
  • Wagenaar I; Dept. of Public Health, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Post E; KIT Health, Royal Tropical Institute, Amsterdam, the Netherlands.
  • Brandsma W; Independent Leprosy Consultant, Royal Tropical Institute, Amsterdam, the Netherlands.
  • Bowers B; Rural Health Program, The Leprosy Mission International Bangladesh, Nilphamari, Bangladesh.
  • Alam K; Menzies Health Institute Queensland, Griffith University, Brisbane, Australia.
  • Shetty V; Rural Health Program, The Leprosy Mission International Bangladesh, Nilphamari, Bangladesh.
  • Pai V; Foundation for Medical Research, Mumbai, India.
  • Husain S; Bombay Leprosy Project, Mumbai, India.
  • Sigit Prakoeswa CR; JALMA institute of Leprosy & Other Mycobacterial Diseases, Agra, India.
  • Astari L; Dermatovenereology Dept., Dr Soetomo Hospital-Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
  • Hagge D; Dermatovenereology Dept., Dr Soetomo Hospital-Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
  • Shah M; Anandaban Hospital and Mycobacterial Research Laboratories, The Leprosy Mission Nepal, Kathmandu, Nepal.
  • Neupane K; Anandaban Hospital and Mycobacterial Research Laboratories, The Leprosy Mission Nepal, Kathmandu, Nepal.
  • Tamang KB; Anandaban Hospital and Mycobacterial Research Laboratories, The Leprosy Mission Nepal, Kathmandu, Nepal.
  • Richardus JH; Faculty of Health Sciences, University of Southampton, Southampton, United Kingdom.
PLoS Negl Trop Dis ; 11(10): e0005952, 2017 Oct.
Article em En | MEDLINE | ID: mdl-28976976
ABSTRACT

BACKGROUND:

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:

In 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.

RESULTS:

We 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.

CONCLUSION:

In 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.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Prednisolona / Doenças do Sistema Nervoso Periférico / Hanseníase / Anti-Inflamatórios Tipo de estudo: Clinical_trials / Etiology_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS Negl Trop Dis Assunto da revista: MEDICINA TROPICAL Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Prednisolona / Doenças do Sistema Nervoso Periférico / Hanseníase / Anti-Inflamatórios Tipo de estudo: Clinical_trials / Etiology_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS Negl Trop Dis Assunto da revista: MEDICINA TROPICAL Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda