表征与BPaLM方案相关的肌肉骨骼和神经毒性:多药耐药结核病(MDR-TB)患者关节痛和周围神经病变的临床评估

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2025-06-17 eCollection Date: 2025-06-01 DOI:10.7759/cureus.86248
Zahir Khan, Gohar Ali, Rumman, Ashraf, Akmal Naveed, Shahid Salam, Ubaid Ullah, Ahmad Ismail, Afrasyab Altaf
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引用次数: 0

摘要

背景:BPaLM(贝达喹啉、普雷托马尼、利奈唑胺和莫西沙星)方案是一种新兴的耐多药结核病(MDR-TB)治疗方案,其常见的副作用是肌肉骨骼和神经系统毒性。这些毒性,特别是关节痛和周围神经病变,可显著损害接受治疗的患者的生活质量。尽管BPaLM方案有很好的治疗效果,但这些副作用的流行程度和严重程度仍未得到充分探讨。了解这些毒性对于改善患者管理策略和确保更好的治疗依从性至关重要。目的:本研究旨在确定接受BPaLM方案治疗的耐多药结核病患者中常见和严重的肌肉骨骼和神经毒性,特别是关节痛和周围神经病变。材料和方法:本前瞻性观察性研究于2024年1月至2025年4月在马尔丹医疗中心耐药结核病规划管理中心进行。接受BPaLM方案治疗的耐多药结核病患者监测肌肉骨骼和神经毒性,特别是关节痛和周围神经病变。临床评估包括评估关节疼痛和神经损伤的发病、严重程度和影响,以及评估疼痛管理和物理治疗干预的有效性。数据收集包括人口统计信息、合并症和基线体力活动水平。使用SPSS Statistics version 26 (IBM Corp. 2019年发布)进行统计分析。IBM SPSS Statistics for Windows, Version 26.0。Armonk, NY: IBM公司),Python (Python软件基金会,Beaverton, OR, USA)和R 4.4.5 (R Foundation for Statistical Computing, Vienna, Austria),通过描述性统计,卡方检验和决策树建模来识别毒性严重程度的重要预测因子。Kaplan-Meier生存分析也用于评估毒性严重程度与治疗结果之间的关系。结果:44例耐多药结核病患者中,有35例(79.54%)出现轻中度关节痛,其中膝关节疼痛最为常见(34例,77.27%)。周围神经病变26例(59.09%),下肢病变20例(45.45%)。Kaplan-Meier生存分析显示,基于关节痛和周围神经病变严重程度的生存时间存在显著差异,症状更严重与生存时间缩短相关。结论:研究结果强调了早期识别、定期监测和个性化管理策略的重要性,以减轻这些毒性的负担并提高患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterizing Musculoskeletal and Neurological Toxicities Associated With the BPaLM Regimen: A Clinical Evaluation of Arthralgia and Peripheral Neuropathy in Patients With Multidrug-Resistant Tuberculosis (MDR-TB).

Background: Musculoskeletal and neurological toxicities are common side effects of the BPaLM (bedaquiline, pretomanid, linezolid, and moxifloxacin) regimen, an emerging treatment for multidrug-resistant tuberculosis (MDR-TB). These toxicities, particularly arthralgia and peripheral neuropathy, can significantly impair the quality of life of patients undergoing treatment. Despite the promising therapeutic benefits of the BPaLM regimen, the prevalence and severity of these side effects remain underexplored. Understanding these toxicities is crucial to improving patient management strategies and ensuring better treatment adherence.

Objective: This study aims to determine how common and severe musculoskeletal and neurological toxicities, particularly arthralgia and peripheral neuropathy, are among MDR-TB patients treated with the BPaLM regimen.

Materials and methods: This prospective observational study was conducted at the Programmatic Management of Drug-Resistant Tuberculosis in Mardan Medical Complex between January 2024 and April 2025. Patients with MDR-TB undergoing treatment with the BPaLM regimen were monitored for musculoskeletal and neurological toxicities, specifically arthralgia and peripheral neuropathy. Clinical evaluations included assessing the onset, severity, and impact of joint pain and nerve damage, as well as evaluating the effectiveness of pain management and physical therapy interventions. Data collection included demographic information, comorbidities, and baseline physical activity levels. Statistical analysis was performed using SPSS Statistics version 26 (IBM Corp. Released 2019. IBM SPSS Statistics for Windows, Version 26.0. Armonk, NY: IBM Corp.), Python (Python Software Foundation, Beaverton, OR, USA), and R 4.4.5 (R Foundation for Statistical Computing, Vienna, Austria) to identify significant predictors of toxicity severity through descriptive statistics, chi-square tests, and decision tree modeling. Kaplan-Meier survival analysis was also conducted to assess the relationship between toxicity severity and treatment outcomes.

Results: Among the 44 MDR-TB patients, 35 (79.54%) experienced mild to moderate arthralgia, with knee pain being most common (34, 77.27%). Peripheral neuropathy was reported in 26 (59.09%) patients, with the lower limbs (20, 45.45%) being most affected. Kaplan-Meier survival analysis revealed a significant difference in survival times based on the severity of arthralgia and peripheral neuropathy, with more severe symptoms correlating with reduced survival duration.

Conclusions: The findings underscore the importance of early identification, regular monitoring, and personalized management strategies to mitigate the burden of these toxicities and enhance patient outcomes.

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