Marasine Nirmal Raj, Sankhi Sabina, Lamichhane Rajendra
Pharmaceutical Sciences Program, School of Health and Allied Sciences, Pokhara University, Pokhara-30, Kaski, Nepal.
Western Health Science Academy, Pokhara, Kaski, Nepal.
Hosp Pharm. 2022 Feb;57(1):26-31. doi: 10.1177/0018578720970465. Epub 2020 Nov 9.
We aimed to evaluate the impact of pharmaceutical service intervention on medication adherence and patient-reported outcomes among patients diagnosed with depression in a private psychiatric hospital in Nepal. A single-center, open trial with a parallel design was conducted among 18 to 65 years aged patients, diagnosed with depression and under antidepressant medication(s) for ≥2 months. Patients were randomised into either the intervention or control group. The control group (n = 98) received the usual care, while the intervention group (n = 98) received a pharmaceutical service intervention. The two groups were compared using the Mann-Whitney test, independent -test, or chi-square test at 2 and 4 months for changes in medication adherence and patient-reported [severity of depression and health-related quality of life (HRQoL)] outcomes. One hundred ninety adult patients were enrolled in the study. At baseline, there were no significant differences in any of the outcome measures between the intervention and control groups. At 2 and 4 months, the intervention group had a significant improvement only in medication adherence ( < .001) compared with the control group [MGL score: 1 (2) vs 2 (2) and 1 (1) vs 2 (1), < .001, respectively]. Our study suggests that a brief pharmaceutical service intervention in the hospital setting can have a significant impact on patients' adherence to antidepressants but does not improve their severity of depression and HRQoL.
我们旨在评估在尼泊尔一家私立精神病医院中,药学服务干预对确诊为抑郁症患者的用药依从性及患者报告结局的影响。在18至65岁、确诊为抑郁症且服用抗抑郁药≥2个月的患者中开展了一项单中心、平行设计的开放试验。患者被随机分为干预组或对照组。对照组(n = 98)接受常规护理,而干预组(n = 98)接受药学服务干预。在2个月和4个月时,使用曼-惠特尼检验、独立样本t检验或卡方检验比较两组在用药依从性以及患者报告的[抑郁严重程度和健康相关生活质量(HRQoL)]结局方面的变化。本研究共纳入190名成年患者。在基线时,干预组和对照组在任何结局指标上均无显著差异。在2个月和4个月时,与对照组相比,干预组仅在用药依从性方面有显著改善(P <.001)[MGL评分:分别为1(2)对2(2)和1(1)对2(1),P <.001]。我们的研究表明,在医院环境中进行简短的药学服务干预可对患者的抗抑郁药依从性产生显著影响,但不能改善其抑郁严重程度和健康相关生活质量。