Lalashowi Julieth, Mvungi Happiness, Mwaisango Zawadi, Pamba Doreen, Mohamed Athuman, Gitige Catherine, Shayo Pendomartha Joseph, Lekule Isaac, Omary Hamim, Kisonga Riziki, Matechi Emmanuel, Mpagama Stellah G, Olomi Willyhelmina, Ntinginya Nyanda Elias, Kalolo Albino
Tuberculosis and Emerging Diseases, National Institute for Medical Research, Mbeya Medical Research Center, Mbeya, Tanzania, United Republic of.
Medical, Kibong'oto Infectious Diseases Hospital, Sanya Juu, Tanzania, United Republic of.
BMJ Open. 2025 Mar 4;15(3):e088556. doi: 10.1136/bmjopen-2024-088556.
To determine patients' acceptability, satisfaction and adherence to shorter all-oral multidrug-resistant tuberculosis (MDR-TB) regimen in Tanzania.
A two-phase cross-sectional study with data collected within 6 months of Removed Injectable modified Short-course regimens for EXpert MDR-TB (RISE) study implementation and the second phase within 15 months of implementation using the same reference populations.
18 health facilities across eight regions of Tanzania.
Rifampicin-resistant TB/MDR-TB patients enrolled in the RISE study.
We assessed patients' acceptability, adherence and satisfaction with the regimen using an interval scale structured questionnaire.
The majority of the patients found the shorter oral MDR-TB treatment acceptable, adhered to it well and were generally satisfied. The median score (IQR) for acceptability was 1.7 (1.03-2.00) but it ranged between 1.3 (1.3-2) and 1.7 (1-1.79) for the first and second phases, respectively. Regarding adherence, the median score (IQR) stood at 4 (3.67-4.67) with scores significantly higher in the second phase at 4.33 (4.00-5.007) compared with the first at 4.67 (4.00-5.0), p value=0.01. The overall satisfaction was high at 1.5 (1.33-1.78) but it ranged between 1.22 (1.00-1.78) and 1.42 (1.11-1.78) for the first and second phases, respectively. Worrying about side effects was statistically associated with adherence (p value<0.05). No statistically significant associations were found for acceptability and satisfaction.
Generally, the modified shorter oral MDR-TB regimen was accepted, and patients reported good adherence and were satisfied. More engagement with patients could provide more insights into factors that can maximise acceptability, adherence and satisfaction with the regimen.
确定坦桑尼亚患者对较短程全口服耐多药结核病(MDR-TB)治疗方案的可接受性、满意度和依从性。
一项两阶段横断面研究,数据收集于专家耐多药结核病短程治疗方案(RISE)实施的6个月内,第二阶段数据收集于实施的15个月内,使用相同的参考人群。
坦桑尼亚八个地区的18个卫生设施。
纳入RISE研究的利福平耐药结核病/MDR-TB患者。
我们使用间隔量表结构化问卷评估患者对该治疗方案的可接受性、依从性和满意度。
大多数患者认为较短程口服MDR-TB治疗方案可接受,依从性良好,总体满意。可接受性的中位数(四分位间距)为1.7(1.03-2.00),但第一阶段和第二阶段分别在1.3(1.3-2)和1.7(1-1.79)之间。关于依从性,中位数(四分位间距)为4(3.67-4.67),第二阶段得分显著高于第一阶段,分别为4.33(4.00-5.007)和4.67(4.00-5.0),p值=0.01。总体满意度较高,为1.5(1.33-1.78),但第一阶段和第二阶段分别在1.22(1.00-1.78)和1.42(1.11-1.78)之间。担心副作用与依从性存在统计学关联(p值<0.05)。未发现可接受性和满意度存在统计学显著关联。
总体而言,改良后的较短程口服MDR-TB治疗方案被接受,患者报告依从性良好且满意。与患者进行更多互动可以更深入了解能够最大限度提高对该治疗方案的可接受性、依从性和满意度的因素。