Minimising the risks of allergen-specific injection immunotherapy

被引:50
作者
Malling, HJ [1 ]
机构
[1] Univ Copenhagen, Natl Hosp, Allergy Unit 7551, DK-2100 Copenhagen, Denmark
关键词
D O I
10.2165/00002018-200023040-00005
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The clinical advantages of allergen-specific immunotherapy are counterbalanced by the risk of inducing systemic adverse effects. Although the frequency of life-threatening systemic reactions is low, the treatment carries a risk of inducing anaphylactic reactions. A fundamental point in risk assessment is to use a clinically meaningful and internationally accepted grading system for reactions. Of importance in minimising the risk of systemic adverse effects is the identification of at-risk patients and factors, the institution of procedures for monitoring patients before injections, and the adjustment of dosages in accordance with defined rules. Asthma, especially uncontrolled asthma, is a significant risk factor for the induction of systemic reactions. Likewise, dose escalation during allergen exposure, i.e. during pollen seasons, increases the risk of adverse effects. It is recommended that standardised extracts with a documented potency and consistency between production batches are used in order to prevent overdose when changing to a new vial. The intensity of the induction regimen is a balance between the risk of inducing systemic reactions and the time required to administer the regimen. Single injections once a week are generally well tolerated, in contrast to rush immunotherapy which may carry an increased frequency of adverse effects. A clustered induction regimen (2 to 4 injections per visit) represents a compromise of a patient-friendly fast regimen without an unacceptably high frequency of systemic reactions. A major issue in improving the safety of allergen injections is minimising the human factor, e.g. mistakes of patient identification, allergen extracts and dosages. Meticulous care in monitoring every patient before the injection, which requires education and training of the staff in the dosage decision process, is the cornerstone in reducing adverse effects. Involving the patient actively in the safety monitoring process might be helpful and improves patient compliance by allowing the patient to be an active partner in the treatment. Finally, if anaphylactic reactions are induced, a successful outcome is related to the staff being able to identify the early signs and to institute immediate rescue treatment. A quality assurance programme is the optimal way to minimise the risk of immunotherapy-associated systemic reactions.
引用
收藏
页码:323 / 332
页数:10
相关论文
共 27 条
[1]   RAPID HYMENOPTERA VENOM IMMUNOTHERAPY - COMPARATIVE SAFETY OF 3 PROTOCOLS [J].
BIRNBAUM, J ;
CHARPIN, D ;
VERVLOET, D .
CLINICAL AND EXPERIMENTAL ALLERGY, 1993, 23 (03) :226-230
[2]   SAFETY CONSIDERATIONS IN ASSESSING THE ROLE OF IMMUNOTHERAPY IN ALLERGIC DISORDERS [J].
BOUSQUET, J ;
MICHEL, FB .
DRUG SAFETY, 1994, 10 (01) :5-17
[3]   IMMUNOTHERAPY WITH A STANDARDIZED DERMATOPHAGOIDES-PTERONYSSINUS EXTRACT .3. SYSTEMIC REACTIONS DURING THE RUSH PROTOCOL IN PATIENTS SUFFERING FROM ASTHMA [J].
BOUSQUET, J ;
HEJJAOUI, A ;
DHIVERT, H ;
CLAUZEL, AM ;
MICHEL, FB .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 83 (04) :797-802
[4]   SPECIFIC IMMUNOTHERAPY WITH A STANDARDIZED DERMATOPHAGOIDES-PTERONYSSINUS EXTRACT .2. PREDICTION OF EFFICACY OF IMMUNOTHERAPY [J].
BOUSQUET, J ;
HEJJAOUI, A ;
CLAUZEL, AM ;
GUERIN, B ;
DHIVERT, H ;
SKASSABROCIEK, W ;
MICHEL, FB .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1988, 82 (06) :971-977
[5]  
Bousquet J., 1998, Allergy (Copenhagen), V53, P1
[6]   Minimal persistent inflammation is present at mucosal level in patients with asymptomatic rhinitis and mite allergy [J].
Ciprandi, G ;
Buscaglia, S ;
Pesce, G ;
Pronzato, C ;
Ricca, V ;
Parmiani, S ;
Bagnasco, M ;
Canonica, GW .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1995, 96 (06) :971-979
[7]   POSITION PAPER - ALLERGEN STANDARDIZATION AND SKIN-TESTS [J].
DREBORG, S ;
FREW, A .
ALLERGY, 1993, 48 (14) :49-82
[8]   LATE AND IMMEDIATE SYSTEMIC-ALLERGIC REACTIONS TO INHALANT ALLERGEN IMMUNOTHERAPY [J].
GREENBERG, MA ;
KAUFMAN, CR ;
GONZALEZ, GE ;
ROSENBLATT, CD ;
SMITH, LJ ;
SUMMERS, RJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1986, 77 (06) :865-870
[9]   A CONTROLLED DOSE-RESPONSE STUDY OF IMMUNOTHERAPY WITH STANDARDIZED, PARTIALLY PURIFIED EXTRACT OF HOUSE DUST MITE - CLINICAL EFFICACY AND SIDE-EFFECTS [J].
HAUGAARD, L ;
DAHL, R ;
JACOBSEN, L .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1993, 91 (03) :709-722
[10]   SYSTEMIC REACTIONS OCCURRING DURING IMMUNOTHERAPY WITH STANDARDIZED POLLEN EXTRACTS [J].
HEJJAOUI, A ;
FERRANDO, R ;
DHIVERT, H ;
MICHEL, FB ;
BOUSQUET, J .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (05) :925-933