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重庆大学附属黔江医院眼科
纸质出版日期:2022,
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冉建川, 龙正勤, 任佑凡, 等. 利妥昔单抗治疗复发性原发性干燥综合征相关性干眼的疗效观察[J]. 中国医院用药评价与分析, 2022,(12):1455-1458.
RAN Jianchuan, LONG Zhengqin, REN Youfan, et al. Efficacy of Rituximab in the Treatment of Recurrent Primary Sj?gren Syndrome Associated Dry Eye[J]. 2022,(12):1455-1458.
冉建川, 龙正勤, 任佑凡, 等. 利妥昔单抗治疗复发性原发性干燥综合征相关性干眼的疗效观察[J]. 中国医院用药评价与分析, 2022,(12):1455-1458. DOI: 10.14009/j.issn.1672-2124.2022.12.006.
RAN Jianchuan, LONG Zhengqin, REN Youfan, et al. Efficacy of Rituximab in the Treatment of Recurrent Primary Sj?gren Syndrome Associated Dry Eye[J]. 2022,(12):1455-1458. DOI: 10.14009/j.issn.1672-2124.2022.12.006.
目的:探讨利妥昔单抗治疗复发性原发性干燥综合征(pSS)相关性干眼的疗效,为临床治疗提供参考。方法:选择2015年1月至2021年8月该院收治的复发性pSS相关性干眼患者81例,采用随机数字表法将患者分为两组。对照组患者(41例,82眼)采用醋酸泼尼、硫酸羟氯喹、环磷酰胺全身用药以及局部滴眼液保护治疗8周;观察组患者(40例,80眼)在对照组的基础上静脉滴注利妥昔单抗375 mg/m~2
1周1次,共治疗8周。观察两组患者治疗前后标准干眼症状评估(SPEED)问卷评分、泪膜破裂时间、SchirmerⅠ泪液分泌实验和角膜荧光素染色评分,记录不良反应和随访期间的复发情况。结果:两组患者治疗后的SPEED眼部干涩感、异物感、疼痛、烧灼感或流泪评分和总分,角膜荧光素染色评分较治疗前明显降低,泪膜破裂时间较治疗前延长,SchirmerⅠ泪液分泌浸湿滤纸长度较治疗前增加,差异均有统计学意义(P<0.01)。观察组患者治疗后的SPEED眼部干涩感[(2.15±0.36)分vs.(3.26±0.47)分]、异物感[(2.11±0.28)分vs.(3.02±0.40)分]、疼痛[(2.03±0.28)分vs.(2.95±0.36)分]、烧灼感或流泪[(1.26±0.24)分vs.(2.15±0.39)分]评分和总分[(7.55±1.46)分vs.(11.38±2.74)分]
角膜荧光素染色评分[(3.11±0.53)分vs.(4.02±0.69)分]低于对照组,泪膜破裂时间[(9.57±2.03)s vs.(7.35±1.95)s]长于对照组,SchirmerⅠ泪液分泌浸湿滤纸长度[(8.97±2.17) mm vs.(6.95±1.72) mm]大于对照组,差异均有统计学意义(P<0.01)。观察组患者的复发率[5.00%(2/40)vs. 24.39%(10/41)]低于对照组,差异有统计学意义(P<0.05)。两组患者不良反应发生率的差异无统计学意义(P>0.05)。结论:与传统治疗比较,利妥昔单抗治疗复发性pSS相关性干眼患者,可显著促使泪腺分泌,改善干眼症状,降低复发风险。
OBJECTIVE: To probe into the efficacy of rituximab in the treatment of recurrent primary Sj9 gren syndrome(pSS) associated dry eye
so as to provide reference for clinical treatment. METHODS: Totally 81 patients with recurrent pSS associated xerophthalmia admitted into this hospital from Jan. 2015 to Aug. 2021 were selected and divided into two groups by random number table. The control group(41 cases
82 eyes) was given prednisone acetate
hydroxychloroquine sulfate and cyclophosphamide for systemic administration and topical eye drops for 8 weeks; while the observation group(40 cases
80 eyes) were given rituximab 375 mg/m~2 for intravenous drip based on the control group
once a week for 8 weeks. Scores of the standard patient evaluation of eye dryness(SPEED) questionnaire
rupture time of tear film
scores of Schirmer Ⅰ tear secretion test and corneal fluorescein staining of the two groups were observed
incidence of adverse drug reactions and recurrence during follow-up were recorded. RESULTS: After treatment
the SPEED scores of eye dryness
foreign body sensation
pain
burning sensation or tearing and total score
and scores of corneal fluorescein staining of both groups were significantly lower than before treatment
the rupture time of tear film was longer than before treatment
and the length of Schirmer I tear secretion-soaked filter paper was increased compared with before treatment in both groups
with statistically significant differences(P<0.01). The SPEED scores of eye dryness [(2.15±0.36) points vs.(3.26±0.47) points]
foreign body sensation [(2.11±0.28) points vs.(3.02±0.40) points]
pain [(2.03±0.28) points vs.(2.95±0.36) points]
burning sensation or tearing [(1.26±0.24) points vs.(2.15±0.39) points] and total score [(7.55±1.46) points vs.(11.38±2.74) points]
and scores of corneal fluorescein staining [(3.11±0.53) points vs.(4.02±0.69) points] of the observation group were lower than those of the control group after treatment
and the rupture time of tear film [(9.57±2.03) s vs.(7.35±1.95) s] of the observation group was longer than that of the control group
the length of Schirmer Ⅰ tear secretion-soaked filter paper [(8.97±2.17) mm vs.(6.95±1.72) mm] of the observation group was greater than that of the control group
with statistically significant differences(P<0.01). The recurrence rate of the observation group [5.00%(2/40) vs. 24.39%(10/41)] was lower than that of the control group
with statistically significant difference(P<0.05). The difference in the incidences of adverse drug reactions between two groups was not statistically significant(P>0.05). CONCLUSIONS: Compared with conventional treatment
the application of rituximab for recurrent pSS associated dry eye can significantly induced lacrimal secretion
improved dry eye symptoms and reduced the risk of recurrence.
利妥昔单抗B细胞原发性干燥综合征干眼复发
RituximabB cellsPrimary Sj?gren syndromeDry eyeRecurrence
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