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基于BPaL方案治疗耐多药结核病的安全性和有效性:一家意大利结核病转诊医院的首次经验。

Safety and Effectiveness of BPaL-Based Regimens to Treat Multidrug-Resistant TB: First Experience of an Italian Tuberculosis Referral Hospital.

作者信息

Gualano Gina, Musso Maria, Mencarini Paola, Mosti Silvia, Cerva Carlotta, Vittozzi Pietro, Mazzarelli Antonio, Cannas Angela, Navarra Assunta, Ianniello Stefania, Faccendini Paolo, Palmieri Fabrizio

机构信息

Respiratory Infectious Diseases Unit, National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, 00149 Rome, Italy.

Department of Microbiology, National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, 00149 Rome, Italy.

出版信息

Antibiotics (Basel). 2024 Dec 25;14(1):7. doi: 10.3390/antibiotics14010007.

Abstract

: Tuberculosis (TB) is preventable and curable, but multidrug-resistant TB (MDR-TB) and extensively drug-resistant TB (XDR-TB) pose significant challenges worldwide due to the limited treatment options, lengths of therapies, and high rates of treatment failure. The management of MDR-TB has been revolutionized by all oral anti-TB drug regimens that are likely to improve adherence and treatment outcomes. These regimes include bedaquiline (B), pretomanid (P), and linezolid (L) (BPaL), and moxifloxacin if resistance to fluoroquinolones is not detected (BPaLM). Based on the evidence generated by the TB-PRACTECAL and ZeNix randomized controlled trials, BPaL/BPaLM regimens are recommended over the currently recommended longer regimens in patients with MDR-TB or monoresistance to rifampin (RR). To our knowledge, no data are currently available on the implementation of BPaL/BPaLM regimens in Italy. : Seventeen patients completed the BPaL/BPaLM regimen, with a treatment success rate of 90% (17/19), consistent with the literature data. Eleven patients out of the nineteen retained in care (58%) complained about symptoms consistent with adverse events (AEs). No treatment interruption was necessary due to AEs. : Here, we report the real-world experience of a tertiary referral hospital for TB in Italy, from 2022 to 2024, in the management, outcomes, and adverse drug reactions of a cohort of twenty-two MDR/RR patients treated with BPaL and BPaLM regimens. : BPaL-containing regimens also serve as promising options for patients with RR/MDR-TB in terms of real-life experience, but further multicentric studies are required in Europe to confirm the efficacy of shorter regimens to eliminate MDR TB.

摘要

结核病(TB)是可预防和可治愈的,但耐多药结核病(MDR-TB)和广泛耐药结核病(XDR-TB)由于治疗选择有限、治疗疗程长以及治疗失败率高,在全球范围内构成了重大挑战。全口服抗结核药物方案彻底改变了耐多药结核病的管理方式,这些方案可能会提高依从性和治疗效果。这些方案包括贝达喹啉(B)、普瑞玛尼(P)和利奈唑胺(L)(BPaL),如果未检测到对氟喹诺酮类药物的耐药性,则使用莫西沙星(BPaLM)。根据TB-PRACTECAL和ZeNix随机对照试验产生的证据,对于耐多药结核病或对利福平(RR)单耐药的患者,推荐使用BPaL/BPaLM方案,而不是目前推荐的更长疗程方案。据我们所知,目前在意大利尚无关于实施BPaL/BPaLM方案的数据。17名患者完成了BPaL/BPaLM方案,治疗成功率为90%(17/19),与文献数据一致。接受治疗的19名患者中有11名(58%)抱怨出现了与不良事件(AE)一致的症状。无需因不良事件而中断治疗。在此,我们报告了意大利一家三级结核病转诊医院在2022年至2024年期间,对一组接受BPaL和BPaLM方案治疗的22例耐多药/利福平耐药患者的管理、结局和药物不良反应的真实世界经验。就实际经验而言,含BPaL的方案对于利福平耐药/耐多药结核病患者也是有前景的选择,但欧洲需要进一步开展多中心研究,以证实较短疗程方案消除耐多药结核病的疗效。

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