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Safety, effectiveness, and adherence of a short and all-oral treatment regimen for the treatment of rifampicin-resistant tuberculosis in Niger: a study protocol of a pragmatic randomised clinical trial with stratified block randomisation
被引:5
|作者:
Souleymane, Mahamadou Bassirou
[1
]
Decroo, Tom
[2
,3
]
Soumana, Alphazazi
[4
]
Lawan, Ibrahim Maman
[1
]
Gagara-Issoufou, Assiatou
[5
]
Halidou-Moussa, Souleymane
[6
]
Ortuno-Gutierrez, Nimer
[7
]
Adehossi, Eric
[5
]
Mamadou, Saidou
[5
]
Van Deun, Armand
Piubello, Alberto
[1
,7
]
机构:
[1] Damien Fdn, Niamey, Niger
[2] Inst Trop Med, Antwerp, Belgium
[3] Res Fdn Flanders, Brussels, Belgium
[4] Programme Natl Lutte TB, Niamey, Niger
[5] Univ Abdou Moumouni Niamey, Fac Sci Sante, Niamey, Niger
[6] Hop Natl Amirou Boubacar Diallo, Pneumophtysiol, Niamey, Niger
[7] Damien Fdn, Brussels, Belgium
来源:
关键词:
Rifampicin resistance tuberculosis;
All oral treatment;
New anti-tuberculosis drugs;
Niger;
D O I:
10.1186/s13063-022-06912-7
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
BackgroundRifampicin-resistant tuberculosis (RR-TB) treatment requires combination treatment, which frequently causes serious adverse events and globally results in not much more than 60% treatment success. In Niger, a high cure rate was obtained with a RR-TB treatment strategy based on a second-line injectable drug (SLID)-containing Short Treatment Regimen (STR), with linezolid replacing the SLID in patients with ototoxicity. Given the availability of novel anti-tuberculosis drugs, WHO recommends all-oral RR-TB treatment. Considering the high level of success with the Niger treatment strategy, it would only be justified to replace it in case robust evidence shows that the WHO all-oral bedaquiline/linezolid (BDQ/LZD)-containing STR (experimental arm) performs better than the Niger RR-TB treatment strategy, (control arm) in terms of safety, effectiveness and adherence. MethodsA pragmatic randomised clinical trial (RCT) using stratified block randomisation, conducted between April 2021 and March 2024, prospectively enrols participants diagnosed with RR-TB in one of the four RR-TB units of the nation. Depending of the month in which patients are diagnosed with RR-TB, patients with FQ-susceptible RR-TB are enrolled in either the experimental arm or control arm. DiscussionTo increase the feasibility of conducting a RCT, embedded in routine activities of all Niger's RR-TB Units, we used a creative trial design. We randomised by monthly blocks, whereby the regimen used changes every month, using the month of RR-TB diagnosis as stratifying variable. This approach was deemed feasible for Niger's national tuberculosis programme, as it simplifies the work of the clinicians running the RR-TB units. Our creative design may serve as an example for other national programs. Findings will inform national and international RR-TB treatment guidelines, and will also strengthen the evidence-base on how to develop robust RR-TB treatment regimens.
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