Anaphylaxis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who have clinical symptoms of anaphylaxis at our hospital during the study period and have been diagnosed as anaphylactic based on histamine and tryptase levels and skin test results. 2. Patients who have received a full explanation of the purpose of the study in the consent document approved by the Ethical Review Committee, and have given their free written consent. 3. Patients who are able to have blood drawn at the time of the study
Exclusion criteria
Exclusion criteria: Those who believe that even a blood sample of 1ml will have a negative impact on their health.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in the net percentage of activated basophils over time | — |
Countries
Japan
Contacts
Yamagata University Medical School Hospital Department of Anesthesia