Vemuri Deepthi, Garuda Butchi Raju, Gopi S, Kumar T Sateesh, Kumari U Aruna
Department of Neurology, Andhra Medical College/King George Hospital, Visakhapatnam, Andhra Pradesh, India.
Ann Indian Acad Neurol. 2020 Mar-Apr;23(2):215-219. doi: 10.4103/aian.AIAN_243_19. Epub 2020 Feb 25.
Myasthenia gravis (MG) is an autoimmune disorder with a chronic fluctuating course. The outcome measures encapsulate disease severity, functional impact at diagnosis, and objective evaluation of clinical benefit from therapeutic interventions.
To assess the disease severity, correlation between various outcome measures, and to evaluate the short-term outcome at 3 months and 6 months in a cohort of MG patients.
Quantitative myasthenia gravis (QMG) score, myasthenia gravis composite (MGC) score, and myasthenia gravis quality of life-15 (MG-QoL-15) score were applied to 54 patients at first visit, 3 months and 6 months follow-up.
Mean quality of life-15 (QoL-15) score at base line was 15.241. Mean QMG and MGC scores at baseline were 14.63 ± 8.37 and 15.87 ± 9.14, respectively. QMG score showed a strong positive correlation with both MGC and MG-QoL-15 scores. QMG and MGC scores showed a moderate correlation with acetylcholine receptor antibody (AChR Ab) titers. Mean QMG at follow-up was 9.95 ± 5.49 at 3 months and 6.74 ± 4.74 at 6 months. Mean MGC at follow-up was 10.75 ± 5.58 at 3 months and 6.51 ± 4.36 at 6 months.
The combination of physician-evaluated and patient-reported outcome measures provided a more discerning picture of patient status and response to treatment. Incorporating MG outcome measures into clinical practice would aid in modulating therapies.
重症肌无力(MG)是一种病程呈慢性波动的自身免疫性疾病。结局指标涵盖疾病严重程度、诊断时的功能影响以及对治疗干预临床获益的客观评估。
评估一组重症肌无力患者的疾病严重程度、各种结局指标之间的相关性,并评估3个月和6个月时的短期结局。
对54例患者在首次就诊、3个月和6个月随访时应用重症肌无力定量(QMG)评分、重症肌无力综合(MGC)评分和重症肌无力生活质量-15(MG-QoL-15)评分。
基线时生活质量-15(QoL-15)评分的平均值为15.241。基线时QMG和MGC评分的平均值分别为14.63±8.37和15.87±9.14。QMG评分与MGC和MG-QoL-15评分均呈强正相关。QMG和MGC评分与乙酰胆碱受体抗体(AChR Ab)滴度呈中度相关。随访时3个月的平均QMG为9.95±5.49,6个月时为6.74±4.74。随访时3个月的平均MGC为10.75±5.58,6个月时为6.51±4.36。
医生评估和患者报告的结局指标相结合,能更清晰地呈现患者状态及对治疗的反应。将重症肌无力结局指标纳入临床实践将有助于调整治疗方案。