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Support Care Cancer · Feb 2006
Randomized Controlled TrialProspective, double-blind, randomized trial of equimolar mixture of nitrous oxide/oxygen to prevent pain induced by insertion of venous access ports in cancer patients.
- Marie Cécile Douard, Mario di Palma, Patricia d'Agostino, Sylvie Chevret, Irène Kriegel, Bruno Falissard, Patrick Thierry, Brigitte George, Laurence Bussières, and Jean-Louis Misset.
- Department of Anesthesiology, Hopital Saint Louis, AP-HP, Université Paris VII, 1, avenue Claude Vellefaux, 75010, Paris, France. marie-cecile.douard@sls.ap-hop-paris.fr
- Support Care Cancer. 2006 Feb 1;14(2):161-6.
BackgroundTo assess the efficacy of equimolar mixture of nitrous oxide/oxygen (EMNO) to prevent pain induced by venous access ports (VAPs) implantation in cancer patients.Patients And MethodsIn a randomized, double-blind study on an adult population not knowing the effects of EMNO, cancer patients were randomly assigned to breath via a facial mask, EMNO or a placebo mixture comprising 50% oxygen and 50% nitrogen. The primary end-point was the patients' assessment of the severity of pain evaluated using a visual analog scale (VAS, 0 to 100) and the proportion of patients suffering pain in each group. The secondary criteria were side effects, tolerability of EMNO, and the level of satisfaction of both the patients and the medical team.ResultsEighty-three adults (42 in the EMNO group and 41 in the placebo group) were included. VAPs were implanted in the jugular vein in 95% of patients. In the placebo group, 78% of the patients declared that they found VAP implantation painful vs. 34% in the EMNO group (p=0.001). The severity of the pain was reduced by 50% in the EMNO group in comparison with placebo (p=0.0125). Although the median time to perform implantation was strictly identical in both groups (20 min), the estimated duration of surgery seemed longer to patients in the control group. Patient and investigator satisfaction indexes were >90% in both groups.ConclusionEMNO provides an effective solution for the prevention of pain during placement of VAPs.
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