Systemic reactions associated with subcutaneous allergen immunotherapy: timing and risk assessment

Background Subcutaneous allergen immunotherapy (SCIT) is associated with risk of systemic reaction. Although risk factors have been identified, the incidence of immunotherapy-related systemic reactions has not changed in recent years. Objectives To examine patterns of systemic reaction and determine...

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Veröffentlicht in:Annals of allergy, asthma, & immunology asthma, & immunology, 2011-06, Vol.106 (6), p.533-537.e2
Hauptverfasser: DaVeiga, Sigrid Payne, MD, Liu, Xiaobo, MS, Caruso, Kathleen, RN, BSN, Golubski, Susan, LPN, Xu, Meng, MS, Lang, David M., MD
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container_end_page 537.e2
container_issue 6
container_start_page 533
container_title Annals of allergy, asthma, & immunology
container_volume 106
creator DaVeiga, Sigrid Payne, MD
Liu, Xiaobo, MS
Caruso, Kathleen, RN, BSN
Golubski, Susan, LPN
Xu, Meng, MS
Lang, David M., MD
description Background Subcutaneous allergen immunotherapy (SCIT) is associated with risk of systemic reaction. Although risk factors have been identified, the incidence of immunotherapy-related systemic reactions has not changed in recent years. Objectives To examine patterns of systemic reaction and determine whether risk of systemic reaction from SCIT is associated with patterns of response to skin tests to inhalant allergens recorded before receiving SCIT. Methods We carried out a retrospective review from January 2001 to December 2007. Patterns of systemic reaction from immunotherapy were examined. Cases were matched with controls by age (±10 years), sex, and time of injection (±1 week) to determine whether a pattern of more than 33% 3+ and 4+ skin test responses is associated with elevated risk for systemic reaction. Results Rate of systemic reaction from SCIT was 0.28% (46/16,375) per injection visit. Twenty patients had 46 systemic reactions. All severe reactions occurred within 30 minutes. The estimated odds of systemic reaction were almost 6 times higher for patients with more than 33% 3 to 4+ positive skin tests (OR = 5.83; 95%CI: 1.23–27.59, P = .026). For each additional 4+ skin test, the estimated odds for systemic reaction increased by 17% ( P = .020). Conclusions A small number of patients receiving SCIT account for a large proportion of systemic reactions. Skin test patterns demonstrating a greater number of larger skin tests responses to inhalant skin testing are associated with significantly elevated risk for systemic reaction in patients receiving SCIT.
doi_str_mv 10.1016/j.anai.2011.02.007
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Although risk factors have been identified, the incidence of immunotherapy-related systemic reactions has not changed in recent years. Objectives To examine patterns of systemic reaction and determine whether risk of systemic reaction from SCIT is associated with patterns of response to skin tests to inhalant allergens recorded before receiving SCIT. Methods We carried out a retrospective review from January 2001 to December 2007. Patterns of systemic reaction from immunotherapy were examined. Cases were matched with controls by age (±10 years), sex, and time of injection (±1 week) to determine whether a pattern of more than 33% 3+ and 4+ skin test responses is associated with elevated risk for systemic reaction. Results Rate of systemic reaction from SCIT was 0.28% (46/16,375) per injection visit. Twenty patients had 46 systemic reactions. All severe reactions occurred within 30 minutes. The estimated odds of systemic reaction were almost 6 times higher for patients with more than 33% 3 to 4+ positive skin tests (OR = 5.83; 95%CI: 1.23–27.59, P = .026). For each additional 4+ skin test, the estimated odds for systemic reaction increased by 17% ( P = .020). Conclusions A small number of patients receiving SCIT account for a large proportion of systemic reactions. Skin test patterns demonstrating a greater number of larger skin tests responses to inhalant skin testing are associated with significantly elevated risk for systemic reaction in patients receiving SCIT.</description><identifier>ISSN: 1081-1206</identifier><identifier>EISSN: 1534-4436</identifier><identifier>DOI: 10.1016/j.anai.2011.02.007</identifier><identifier>PMID: 21624754</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Allergy and Immunology ; Biological and medical sciences ; Case-Control Studies ; Dermatology ; Desensitization, Immunologic - adverse effects ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Immunopathology ; Inhalation Exposure ; Injections, Subcutaneous ; Male ; Medical sciences ; Retrospective Studies ; Risk Assessment ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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Although risk factors have been identified, the incidence of immunotherapy-related systemic reactions has not changed in recent years. Objectives To examine patterns of systemic reaction and determine whether risk of systemic reaction from SCIT is associated with patterns of response to skin tests to inhalant allergens recorded before receiving SCIT. Methods We carried out a retrospective review from January 2001 to December 2007. Patterns of systemic reaction from immunotherapy were examined. Cases were matched with controls by age (±10 years), sex, and time of injection (±1 week) to determine whether a pattern of more than 33% 3+ and 4+ skin test responses is associated with elevated risk for systemic reaction. Results Rate of systemic reaction from SCIT was 0.28% (46/16,375) per injection visit. Twenty patients had 46 systemic reactions. All severe reactions occurred within 30 minutes. The estimated odds of systemic reaction were almost 6 times higher for patients with more than 33% 3 to 4+ positive skin tests (OR = 5.83; 95%CI: 1.23–27.59, P = .026). For each additional 4+ skin test, the estimated odds for systemic reaction increased by 17% ( P = .020). Conclusions A small number of patients receiving SCIT account for a large proportion of systemic reactions. Skin test patterns demonstrating a greater number of larger skin tests responses to inhalant skin testing are associated with significantly elevated risk for systemic reaction in patients receiving SCIT.</description><subject>Adult</subject><subject>Allergy and Immunology</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Dermatology</subject><subject>Desensitization, Immunologic - adverse effects</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Immunopathology</subject><subject>Inhalation Exposure</subject><subject>Injections, Subcutaneous</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Immunopathology</topic><topic>Inhalation Exposure</topic><topic>Injections, Subcutaneous</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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Although risk factors have been identified, the incidence of immunotherapy-related systemic reactions has not changed in recent years. Objectives To examine patterns of systemic reaction and determine whether risk of systemic reaction from SCIT is associated with patterns of response to skin tests to inhalant allergens recorded before receiving SCIT. Methods We carried out a retrospective review from January 2001 to December 2007. Patterns of systemic reaction from immunotherapy were examined. Cases were matched with controls by age (±10 years), sex, and time of injection (±1 week) to determine whether a pattern of more than 33% 3+ and 4+ skin test responses is associated with elevated risk for systemic reaction. Results Rate of systemic reaction from SCIT was 0.28% (46/16,375) per injection visit. Twenty patients had 46 systemic reactions. All severe reactions occurred within 30 minutes. The estimated odds of systemic reaction were almost 6 times higher for patients with more than 33% 3 to 4+ positive skin tests (OR = 5.83; 95%CI: 1.23–27.59, P = .026). For each additional 4+ skin test, the estimated odds for systemic reaction increased by 17% ( P = .020). Conclusions A small number of patients receiving SCIT account for a large proportion of systemic reactions. Skin test patterns demonstrating a greater number of larger skin tests responses to inhalant skin testing are associated with significantly elevated risk for systemic reaction in patients receiving SCIT.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>21624754</pmid><doi>10.1016/j.anai.2011.02.007</doi><tpages>5</tpages></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Adult
Allergy and Immunology
Biological and medical sciences
Case-Control Studies
Dermatology
Desensitization, Immunologic - adverse effects
Female
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Immunopathology
Inhalation Exposure
Injections, Subcutaneous
Male
Medical sciences
Retrospective Studies
Risk Assessment
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Skin Tests
title Systemic reactions associated with subcutaneous allergen immunotherapy: timing and risk assessment
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