According to some guidelines (Australian and New Zealand Anaesthetic Allergy Group perioperative anaphylaxis investigation guidelines, 2017) allergy tests should be carried out in patients with a history suspicious of chlorhexidine allergy, in patients with allergic reactions in the healthcare setting where exposure to chlorhexidine cannot be excluded with certainty and in all patients with perioperative allergic reactions (7). Allergy to chlorhexidine should be diagnosed based on a relevant clinical reaction in combination with two positive diagnostic tests, according to Danish Anaesthesia Allergy Centre, where sIgE and skin prick test are recommended as the minimum (8).
Although a provocation test is the gold standard for diagnosis of drug allergy in both immediate and delayed types, it is contraindicated in patients with previous severe reactions or anaphylaxis (3).
Chlorhexidine allergy carries unique features:
● Often unrecognized.
● Reaction onset in the perioperative setting varies (rapid or delayed).
● Patients with anaphylaxis have a history of mild localized reaction to earlier exposure.
● A skin test may have to be read 20–30 mins after.
● Single allergy test may be insufficient to exclude allergy.
● May be coincident with other drug allergies.
Investigations for chlorhexidine allergy comprise in vivo and in vitro tests. The tests should be carried out in patients with a history suspicious of chlorhexidine allergy, in patients with allergic reactions in the healthcare setting where exposure to chlorhexidine cannot be excluded with certainty and in all patients with perioperative allergic reactions (3). In a large single-centre study 22 patients with chlorhexidine allergy were identified of 228 patients (9.6%) systematically investigated for suspected perioperative allergic reactions (8).
In vitro diagnostics
In vitro tests include specific IgE test (sIgE), histamine release test (HRT), and basophil activation test (BAT).
Specific IgE: is generally increased in most patients at the time of the reaction. If negative, it should be repeated between 1–4 months after the event. The sensitivity and specificity on the cut-offs recommended by manufacturers range from 84–100% and 93–97%, respectively (3) (9).
HRT and BAT: require a fresh blood sample. Both tests have a sensitivity of 50% and specificity of up to 99% Therefore, they are generally used as additional tests to confirm the diagnosis after other tests have shown equivocal results (3).
In vivo diagnostics
Include skin prick test, intradermal test for immediate reactions and patch tests for delayed reactions.
Skin prick test: a concentration of 5 mg/mL of chlorhexidine di gluconate was recommended. A wheal size of 3 mm or greater developing within 20–30 mins is considered a positive result.
Intradermal test (for immediate reaction): A result is considered positive if the wheal size is 3 mm or greater compared to negative control.
Patch test (for delayed reaction)
Challenge test: No standard protocol of the chlorhexidine challenge test is currently available (3).