anaphylaxis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) The patient whose consent has been obtained in writing with respect to participation in this study 2) The patient showing Grade 2 or severer anaphylactic reactions during perioperative period. In the medical institutions conducting research A only, the subject will be patient showing Grade 3 or severer anaphylactic reactions
Exclusion criteria
Exclusion criteria: 1) The patient who did not give consent for participation 2) The patient who use or have a plan to use unapproved drugs such as investigational drugs 3) The patient to whom a doctor judged inappropriate for participating in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification of causative drug(s) of perioperative anaphylaxis | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence and severity of perioperative anaphylaxis | — |
Countries
Japan
Contacts
Gunma University Hospital Intensive Care Unit