Vapocoolant spray reduces pain scores by Cohen's d -0.30 to -0.48 in critically ill adults during arterial puncture
This randomized controlled trial evaluated pain management during arterial puncture in critically ill adult patients aged 18 years or older. The study population included 201 patients randomized to receive either vapocoolant spray or placebo spray. A total of 194 patients received the allocated intervention, and 192 were included in the final analysis.
The primary outcome measured the intensity of the patient's visual analogue scale rating of pain immediately after the arterial puncture. Results indicated lower pain scores with vapocoolant spray compared to placebo. The effect size was Cohen's d: -0.30 in the best scenario and -0.48 in the worst scenario. The 95% CI for the effect size ranged from -0.58 to -0.01 in the best scenario and -0.77 to -0.19 in the worst scenario.
Safety data indicated no instances of serious adverse events. Patients who withdrew or did not consent to continue were excluded from analysis. Tolerability was described as without significant side effects. Follow-up duration was not reported. The study was conducted in four intensive care units in French hospitals.
The findings suggest a reduction in immediate procedural pain for this specific population. Clinicians should consider the magnitude of the effect when weighing the use of vapocoolant spray in their practice. Further research may be needed to confirm long-term safety and efficacy in broader settings.