Aspirin sensitivity:: Long term follow-up after up to 3 years of adaptive desensitization using a maintenance dose of 100 mg of aspirin a day

被引:45
作者
Gosepath, J [1 ]
Schäfer, D [1 ]
Mann, WJ [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, HNO Klin, D-55101 Mainz, Germany
关键词
aspirin intolerance; in vitro testing; adaptive desensitization; long term results;
D O I
10.1055/s-2002-35002
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background: The full clinical picture of aspirin intolerance, Sampter's triad, is associated with nasal polyposis, clinical sensitivity to most non steroidal and inflammatory drugs (NSAID) and intrinsic bronchial asthma. But the triad can be incomplete and nasal polyposis can be the first clinical symptom of aspirin sensitivity. Although the exact mechanisms of aspirin intolerance as well as those of desensitization remain obscure, an in vitro assay on eicosanoid metabolism has been proven to be helpful in diagnosis and treatment as it correlates well to the individual severity of clinical symptoms. Methods: For this investigation 30 patients, who were undergoing adaptive desensitization for aspirin intolerance, were followed-up between 1 and 3 years. They received a maintenance dose of oral aspirin of only 100 mg a day after an initial application of higher doses. Their clinical course as well as their in vitro parameters of eicosanoid release were monitored throughout the individual observation period. Results: Desensitization was successful in 25 of the 30 patients regarding the recurrence rate of nasal polyps, severity of bronchial asthma and sense of smell. There was a clear positive correlation between clinical and in vitro parameters. Discontinuing of aspirin therapy lead to worsening of clinical symptoms, regardless of the prior duration of treatment. Conclusions: This article reviews the role of the in vitro assay and presents a desensitization protocol that can be maintained as a long term treatment without adverse side effects. Results suggest that the recurrence rate of nasal polyps after surgical therapy can be reduced using this protocol, however, only long term treatment can secure a beneficial outcome over time.
引用
收藏
页码:732 / 738
页数:7
相关论文
共 37 条
[1]   A placebo-controlled, dose-ranging study of montelukast, a cysteinyl leukotriene-receptor antagonist [J].
Altman, LC ;
Munk, Z ;
Seltzer, J ;
Noonan, N ;
Shingo, S ;
Zhang, J ;
Reiss, TF .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1998, 102 (01) :50-56
[2]   AIRWAY RESPONSIVENESS TO HISTAMINE AND LEUKOTRIENE-E4 IN SUBJECTS WITH ASPIRIN-INDUCED ASTHMA [J].
ARM, JP ;
OHICKEY, SP ;
SPUR, BW ;
LEE, TH .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 140 (01) :148-153
[3]   SALICYLATE OTOTOXICITY - REVIEW AND SYNTHESIS [J].
BOETTCHER, FA ;
SALVI, RJ .
AMERICAN JOURNAL OF OTOLARYNGOLOGY, 1991, 12 (01) :33-47
[4]  
BRASCH J, 1994, ALLERGOLOGIE, V17, P197
[5]   Overexpression of leukotriene C4 synthase in bronchial biopsies from patients with aspirin-intolerant asthma [J].
Cowburn, AS ;
Sladek, K ;
Soja, J ;
Adamek, L ;
Nizankowska, E ;
Szczeklik, A ;
Lam, BK ;
Penrose, JF ;
Austen, KF ;
Holgate, ST ;
Sampson, AP .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (04) :834-846
[6]  
GIAMPIERO P, 1991, ANN ALLERGY, V67, P588
[7]   Aspirin intolerance in patients with chronic sinusitis [J].
Gosepath, J ;
Hoffmann, F ;
Schäfer, D ;
Amedee, RG ;
Mann, WJ .
ORL-JOURNAL FOR OTO-RHINO-LARYNGOLOGY AND ITS RELATED SPECIALTIES, 1999, 61 (03) :146-150
[8]   Individual monitoring of aspirin desensitization [J].
Gosepath, J ;
Schaefer, D ;
Amedee, RG ;
Mann, WJ .
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2001, 127 (03) :316-321
[9]   Treatment of ASS-associated polyposis (ASSAP) with a cysteinyl leukotriene receptor antagonist -: A prospective drug study on its antiinflammatory effects [J].
Grundmann, T ;
Töpfner, M .
LARYNGO-RHINO-OTOLOGIE, 2001, 80 (10) :576-582
[10]  
HILKA MB, 1992, HNO, V40, P165