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Midazolam anaphylaxis during general anesthesia
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Abstract
Rationale:
Midazolam is known as a safe drug and is widely used as a sedative and an anesthetic adjuvant. Therefore, there is a lack of awareness that midazolam can cause anaphylaxis. Midazolam anaphylaxis is rare, and only a few cases have been reported, but such a risk is always present. In this study, we report a case of midazolam anaphylaxis by an intravenous injection, in the prone position, during general anesthesia.
Patient concerns:
A 62-year-old woman was intravenously administered 1 mg midazolam during general anesthesia, and sudden severe hypotension, bronchospasm, decreased oxygen saturation, erythema, and diarrhea occurred.
Diagnosis:
Midazolam anaphylaxis was presumptively diagnosed by clinical symptoms and was confirmed by an intradermal test after 9 weeks.
Interventions:
The patient was treated with 100% oxygen, large volume of fluid, epinephrine, phenylephrine, ephedrine, dexamethasone and prednisolone, ranitidine, and flumazenil.
Outcomes:
Severe hypotension and decreased oxygen saturation were resolved within 20 minutes of the onset of anaphylaxis, and the patient was discharged after 3 days without any sequelae.
Lessons:
Midazolam anaphylaxis is very rare, but it can happen always. Therefore, the possibility of anaphylaxis due to midazolam should be considered and always be prepared for treatment.
Ovid Technologies (Wolters Kluwer Health)
Title: Midazolam anaphylaxis during general anesthesia
Description:
Abstract
Rationale:
Midazolam is known as a safe drug and is widely used as a sedative and an anesthetic adjuvant.
Therefore, there is a lack of awareness that midazolam can cause anaphylaxis.
Midazolam anaphylaxis is rare, and only a few cases have been reported, but such a risk is always present.
In this study, we report a case of midazolam anaphylaxis by an intravenous injection, in the prone position, during general anesthesia.
Patient concerns:
A 62-year-old woman was intravenously administered 1 mg midazolam during general anesthesia, and sudden severe hypotension, bronchospasm, decreased oxygen saturation, erythema, and diarrhea occurred.
Diagnosis:
Midazolam anaphylaxis was presumptively diagnosed by clinical symptoms and was confirmed by an intradermal test after 9 weeks.
Interventions:
The patient was treated with 100% oxygen, large volume of fluid, epinephrine, phenylephrine, ephedrine, dexamethasone and prednisolone, ranitidine, and flumazenil.
Outcomes:
Severe hypotension and decreased oxygen saturation were resolved within 20 minutes of the onset of anaphylaxis, and the patient was discharged after 3 days without any sequelae.
Lessons:
Midazolam anaphylaxis is very rare, but it can happen always.
Therefore, the possibility of anaphylaxis due to midazolam should be considered and always be prepared for treatment.
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