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日本批准静脉注射免疫球蛋白前后大疱性类天疱疮患者死亡率和发病率的变化趋势:一项中断时间序列分析。

Trends in mortality and morbidity in patients with bullous pemphigoid before and after approval of intravenous immunoglobulin in Japan: an interrupted time-series analysis.

机构信息

Department of Dermatology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Department of Clinical Epidemiology and Health Economics, School of Public Health, The University of Tokyo, Tokyo, Japan.

出版信息

Clin Exp Dermatol. 2023 Jun 5;48(6):667-673. doi: 10.1093/ced/llad086.

Abstract

BACKGROUND

Intravenous immunoglobulin (IVIg) has been reported to be an effective treatment for bullous pemphigoid. However, the impact of IVIg approval on real-world outcomes remains unclear.

OBJECTIVES

To investigate the effect of IVIg approval on patients with bullous pemphigoid using a national inpatient database.

METHODS

Using the Japanese Diagnosis Procedure Combination database, we identified 14 229 patients admitted to hospital for bullous pemphigoid and treated with systemic corticosteroids between July 2010 and March 2020. We conducted an interrupted time-series analysis to compare in-hospital mortality and morbidity between the patients admitted before and after the approval of reimbursement of IVIg for bullous pemphigoid in the Japanese universal health insurance system in November 2015.

RESULTS

In-hospital mortality was 5.5% before and 4.5% after the approval of IVIg reimbursement. After the IVIg approval, 18% of the patients were treated with IVIg. Based on the interrupted time-series analysis, in-hospital mortality significantly decreased at the time of approval [-1.2%, 95% confidence interval (CI) -2.0 to -0.3, P = 0.009] and a downward trend was observed after the approval (-0.4% annual rate, 95% CI -0.7 to -0.1, P = 0.005). In-hospital morbidity also demonstrated a downward trend after the approval.

CONCLUSIONS

IVIg approval is associated with lower in-hospital mortality and morbidity in inpatients with bullous pemphigoid.

摘要

背景

静脉注射免疫球蛋白(IVIg)已被报道对大疱性类天疱疮有效。然而,IVIg 获批对真实世界结局的影响尚不清楚。

目的

使用国家住院患者数据库研究 IVIg 获批对大疱性类天疱疮患者的影响。

方法

我们利用日本诊断程序组合数据库,确定了 2010 年 7 月至 2020 年 3 月间因大疱性类天疱疮住院并接受全身皮质类固醇治疗的 14229 例患者。我们进行了一项中断时间序列分析,以比较在日本全民健康保险系统于 2015 年 11 月批准报销 IVIg 用于大疱性类天疱疮之前和之后住院患者的院内死亡率和发病率。

结果

批准 IVIg 报销之前的院内死亡率为 5.5%,之后为 4.5%。批准后,18%的患者接受了 IVIg 治疗。基于中断时间序列分析,在批准时院内死亡率显著下降[-1.2%,95%置信区间(CI)-2.0 至 -0.3,P = 0.009],批准后观察到下降趋势(-0.4%的年下降率,95%CI -0.7 至 -0.1,P = 0.005)。批准后,院内发病率也呈下降趋势。

结论

IVIg 获批与大疱性类天疱疮住院患者的院内死亡率和发病率降低相关。

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