RESUMO
AIMS: To evaluate the efficacy and safety of nitrous oxide for children undergoing painful procedures. METHODS: Ninety children requiring repeated painful procedures (lumbar puncture, bone marrow aspirate, venous cannulation, or dressing changes) were given nitrous oxide at a variable concentration of 50-70%. Procedure related distress was evaluated using the Observational Scale of Behavioral Distress-Revised (OSBD-R). OSBD-R scores were obtained for each of the following phases of the procedure: phase 1a, waiting period; phase lb, during induction with nitrous oxide; phase 2, during positioning and cleaning of the skin; phase 3, during the painful procedure; and phase 4, immediately following the procedure and withdrawal of nitrous oxide. Side effects were monitored and recorded by a second observer. RESULTS: OSBD scores reached a maximum during the induction phase with lower scores during subsequent phases. Children over the age of 6 showed a lower level of distress during nitrous oxide administration and the painful procedure. Eighty six per cent of patients had no side effects. The incidence of vomiting, excitement, and dysphoria was 7.8%, 4.4%, and 2% respectively. Eight patients developed oxygen desaturation (SaO(2) < 95%), but none developed hypoxia, airway obstruction, or aspiration. Ninety three per cent of patients fulfilled the criteria for conscious sedation, and 65% had no recollection of the procedure. Mean recovery time was three minutes. CONCLUSIONS: Inhalation of nitrous oxide is effective in alleviating distress during painful procedures, with minimal side effects and short recovery time.
Assuntos
Analgésicos não Narcóticos/uso terapêutico , Ansiedade/tratamento farmacológico , Procedimentos Cirúrgicos Minimamente Invasivos/métodos , Óxido Nitroso/uso terapêutico , Ansiedade/etiologia , Criança , Pré-Escolar , Terapia Cognitivo-Comportamental/métodos , Sonhos , Humanos , Hipóxia/induzido quimicamente , Histeria/induzido quimicamente , Lactente , Procedimentos Cirúrgicos Minimamente Invasivos/efeitos adversos , Oximetria , Medição da Dor , Estudos Prospectivos , Estatísticas não Paramétricas , Resultado do Tratamento , Vômito/induzido quimicamenteRESUMO
Nurse-controlled analgesia (NCA) using a patient-controlled analgesia (PCA) device has been described for intensive care and postoperative use. This report describes the effective use of this technique for severe episodic and procedural pain in four children with advanced malignancy and high opioid requirements where conventional parenteral analgesia had been inadequate. Both morphine and fentanyl were used. Average duration of NCA was 6.75 days (range 4-12).
