Nikose Aishwarya, Patil Swati, Kadhe Neha
Pharmacology and Therapeutics, Lokmanya Tilak Municipal Medical College and General Hospital, Sion, Mumbai, IND.
Clinical Pharmacology, Seth Gordhandas Sunderdas Medical College, Mumbai, IND.
Cureus. 2025 Jan 1;17(1):e76712. doi: 10.7759/cureus.76712. eCollection 2025 Jan.
The primary aim of this study was to investigate the real-world occurrence of various adverse drug reactions (ADRs) and assess medication adherence among patients using disease-modifying antirheumatic drugs (DMARDs). Additionally, the study sought to evaluate the degree of methotrexate intolerance among these patients.
This cross-sectional, observational study was conducted at a tertiary care hospital and involved 100 adult patients diagnosed with rheumatoid arthritis (RA) who were currently undergoing treatment with methotrexate. The study systematically recorded all adverse drug reactions reported by the patients as well as those identified through laboratory tests. Medication adherence was measured using the Compliance Questionnaire Rheumatology (CQR5) and both intentional and non-intentional non-adherence questionnaires. The methotrexate intolerance was assessed using the Methotrexate Intolerance Severity Score (MISS).
Out of the total 74 reported ADRs, gastrointestinal were the most common, accounting for 62 (76.53%) of cases, followed by hematological problems at 13 (16.07%), with other types of ADRs comprising the remaining. Despite the prevalence of gastrointestinal ADRs, the study found high levels of medication adherence among the patients. Additionally, the methotrexate intolerance was relatively low, which may be attributed to the use of folic acid supplementation by all participants.
Gastrointestinal adverse drug reactions were the most frequently observed side effects in this study. Despite these reactions, patients demonstrated a high level of adherence to methotrexate therapy. The factors contributing to this adherence- such as patient counseling, disease knowledge, or the duration of the disease- merit further investigation to understand their impact on treatment outcomes.
本研究的主要目的是调查各种药物不良反应(ADR)在现实世界中的发生情况,并评估使用改善病情抗风湿药(DMARDs)的患者的药物依从性。此外,该研究还试图评估这些患者中氨甲蝶呤不耐受的程度。
这项横断面观察性研究在一家三级护理医院进行,涉及100名被诊断为类风湿性关节炎(RA)且目前正在接受氨甲蝶呤治疗的成年患者。该研究系统记录了患者报告的以及通过实验室检查确定的所有药物不良反应。使用风湿病依从性问卷(CQR5)以及有意和无意不依从问卷来测量药物依从性。使用氨甲蝶呤不耐受严重程度评分(MISS)来评估氨甲蝶呤不耐受情况。
在总共报告的74例药物不良反应中,胃肠道反应最为常见,占62例(76.53%),其次是血液学问题,占13例(16.07%),其他类型的药物不良反应占其余部分。尽管胃肠道药物不良反应普遍存在,但该研究发现患者的药物依从性较高。此外,氨甲蝶呤不耐受情况相对较低,这可能归因于所有参与者都使用了叶酸补充剂。
胃肠道药物不良反应是本研究中最常观察到的副作用。尽管有这些反应,但患者对氨甲蝶呤治疗表现出较高的依从性。促成这种依从性的因素,如患者咨询、疾病知识或疾病持续时间,值得进一步研究以了解它们对治疗结果的影响。