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德国草花粉诱发过敏性鼻炎的过敏免疫疗法处方趋势:一项回顾性队列分析。

Allergy immunotherapy prescribing trends for grass pollen-induced allergic rhinitis in Germany: a retrospective cohort analysis.

作者信息

McDonell Amanda L, Wahn Ulrich, Demuth Dirk, Richards Catrina, Hawes Charlie, Andreasen Jakob Nørgaard, Allen-Ramey Felicia

机构信息

Real-World Evidence Solutions and Health Economics & Outcomes Research, IMS Health, 210 Pentonville Road, London, N1 9JY UK.

Department for Pediatric Pneumology and Immunology, Charité Medical University, Berlin, Germany.

出版信息

Allergy Asthma Clin Immunol. 2015 Jun 10;11(1):19. doi: 10.1186/s13223-015-0085-x. eCollection 2015.

Abstract

BACKGROUND

Allergy immunotherapy is an effective treatment for patients with allergic rhinitis whose symptoms are unresolved with pharmacotherapy. Allergy immunotherapy for grass pollen-induced allergic rhinitis is available in three modalities: subcutaneous immunotherapy and sublingual immunotherapy as a tablet or drop. This study aimed to understand trends in allergy immunotherapy prescribing and practice patterns for grass allergies in adult and paediatric patients in Germany.

METHODS

A retrospective cohort study was conducted using IMS Disease Analyzer in Germany. Patients with an allergy immunotherapy prescription for grass pollen (Anatomical Therapeutic Chemical [ATC] classification code V01AA02) from September 2005 to December 2012 were included in the study. General Practitioners (GPs), dermatologists, Ear, Nose and Throat (ENT)-specialists, paediatricians and pneumologists were included as the allergy immunotherapy prescribing physicians in the study. Descriptive analyses were conducted on patient characteristics at index and prescribing physician specialty; a test for trend was conducted for timing of initiation of first allergy immunotherapy prescription in each annual prescribing season.

RESULTS

Eighteen thousand eight hundred fifty eligible patients were identified during the study period. The majority of patients received subcutaneous immunotherapy; however, the proportion of patients receiving sublingual immunotherapy tablets increased from 8 % in 2006/2007 to 29 % in 2011/2012 (p < 0.001). Initiation of subcutaneous immunotherapy and Oralair® generally peaked during each prescribing year in two seasons (September-October and January) while GRAZAX® prescriptions peaked in autumn (September-October). ENT-specialists and dermatologists were the largest allergy immunotherapy prescribers in adults, while paediatricians and ENT-specialists were the largest prescribers of allergy immunotherapy in paediatric patients.

CONCLUSIONS

Subcutaneous immunotherapy remained the dominant allergy immunotherapy modality for grass pollen-induced allergic rhinitis in Germany for adult and paediatric patients; however, there was a marked increase in proportion of patients receiving sublingual immunotherapy tablets from 2006/2007 to 2011/2012, after their introduction to the market in 2006. ENT-specialists, dermatologists and paediatricians were responsible for the majority of prescribing. The predominance of particular modalities within certain physician specialties likely reflects different treatment goals or needs.

摘要

背景

变应性免疫疗法是治疗药物治疗后症状仍未缓解的变应性鼻炎患者的一种有效方法。针对草花粉诱发的变应性鼻炎的变应性免疫疗法有三种形式:皮下免疫疗法以及舌下含服片剂或滴剂免疫疗法。本研究旨在了解德国成人和儿童患者草过敏变应性免疫疗法的处方趋势和实践模式。

方法

在德国使用IMS疾病分析器进行一项回顾性队列研究。研究纳入了2005年9月至2012年12月期间有草花粉变应性免疫疗法处方(解剖治疗学化学[ATC]分类代码V01AA02)的患者。研究中包括全科医生(GP)、皮肤科医生、耳鼻喉(ENT)专科医生、儿科医生和呼吸科医生作为变应性免疫疗法的处方医生。对索引时的患者特征和处方医生专业进行描述性分析;对每个年度处方季节首次变应性免疫疗法处方开始的时间进行趋势检验。

结果

在研究期间共识别出18850名符合条件的患者。大多数患者接受皮下免疫疗法;然而,接受舌下含服免疫疗法片剂的患者比例从2006/2007年的8%增加到2011/2012年的29%(p<0.001)。皮下免疫疗法和奥罗那®(Oralair®)的处方通常在每个处方年度的两个季节(9月至10月和1月)达到峰值,而葛兰素史克公司生产的格拉扎克斯®(GRAZAX®)处方在秋季(9月至10月)达到峰值。ENT专科医生和皮肤科医生是成人变应性免疫疗法的最大处方者,而儿科医生和ENT专科医生是儿童患者变应性免疫疗法的最大处方者。

结论

在德国,对于成人和儿童患者,皮下免疫疗法仍然是草花粉诱发的变应性鼻炎的主要变应性免疫疗法形式;然而,自2006年舌下含服免疫疗法片剂上市后,2006/2007年至2011/2012年期间接受该疗法的患者比例显著增加。ENT专科医生、皮肤科医生和儿科医生负责大部分处方。某些医生专业中特定疗法的主导地位可能反映了不同的治疗目标或需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a33/4470112/ad504189ee2c/13223_2015_85_Fig1_HTML.jpg

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