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囊性纤维化患者中曲霉菌致敏和变应性支气管肺曲霉菌病的患病率:系统评价和荟萃分析

Prevalence of Aspergillus sensitization and allergic bronchopulmonary aspergillosis in cystic fibrosis: systematic review and meta-analysis.

作者信息

Maturu V N, Agarwal R

机构信息

Department of Pulmonary Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Clin Exp Allergy. 2015 Dec;45(12):1765-78. doi: 10.1111/cea.12595.

Abstract

BACKGROUND

The prevalence of Aspergillus sensitization (AS) and allergic bronchopulmonary aspergillosis (ABPA) in cystic fibrosis (CF) has been varyingly reported. The aim of this systematic review was to estimate the overall prevalence of AS/ABPA in CF.

METHODS

We searched the PubMed and EmBase databases for studies reporting the prevalence of AS/ABPA in CF. We calculated the proportion with 95% confidence interval (CI) to assess the prevalence of AS and ABPA in the individual studies and then pooled the results using a random effects model. Statistical heterogeneity was assessed using the I2 test while publication bias was assessed using both graphical and statistical methods.

RESULTS

Our search yielded 64 eligible studies. The pooled prevalence of AS was 39.1% (95% CI: 33.3-45.1) and was higher with skin test compared to specific IgE (43.8% vs. 32.8%, P = 0.002); however, the prevalence did not vary with the type of skin test used (intradermal or percutaneous). The prevalence of ABPA was 8.9% (95% CI: 7.4-10.7) and was higher in adults as compared to children (10.1% vs. 8.9%, P < 0.0001). There was a wide variation in the criteria used for diagnosing ABPA. Almost 50% (12/23) of the publications after 2004 used criteria other than the CF foundation criteria for diagnosing ABPA. There was significant statistical heterogeneity and evidence of publication bias.

CONCLUSIONS

There is a high prevalence of AS and ABPA in patients with CF. Despite six decades of research, there is still a need to adopt uniform methodology and criteria for the diagnosis of AS/ABPA.

摘要

背景

关于囊性纤维化(CF)患者中曲霉菌致敏(AS)和变应性支气管肺曲霉菌病(ABPA)的患病率,已有不同的报道。本系统评价的目的是估计CF患者中AS/ABPA的总体患病率。

方法

我们在PubMed和EmBase数据库中检索报告CF患者中AS/ABPA患病率的研究。我们计算了95%置信区间(CI)的比例,以评估各研究中AS和ABPA的患病率,然后使用随机效应模型汇总结果。使用I²检验评估统计异质性,同时使用图形和统计方法评估发表偏倚。

结果

我们的检索产生了64项符合条件的研究。AS的汇总患病率为39.1%(95%CI:33.3-45.1),与特异性IgE相比,皮肤试验的患病率更高(43.8%对32.8%,P = 0.002);然而,患病率并不随所使用的皮肤试验类型(皮内或经皮)而变化。ABPA的患病率为8.9%(95%CI:7.4-10.7),成人患病率高于儿童(10.1%对8.9%,P < 0.0001)。诊断ABPA所使用的标准存在很大差异。2004年后几乎50%(12/23)的出版物使用了CF基金会标准以外的标准来诊断ABPA。存在显著的统计异质性和发表偏倚的证据。

结论

CF患者中AS和ABPA的患病率很高。尽管经过了六十年的研究,但仍需要采用统一的方法和标准来诊断AS/ABPA。

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