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Ann Fr Anesth Reanim · Jun 2000
Clinical Trial[Clinical evaluation of alarm efficieny in intensive care].
- L Biot, P Y Carry, J P Perdrix, A Eberhard, and P Baconnier.
- Département d'anesthésie-réanimation, centre hospitalier Lyon Sud, Pierre-Bénite, France.
- Ann Fr Anesth Reanim. 2000 Jun 1;19(6):459-66.
ObjectiveTo evaluate the efficiency of haemodynamic and respiratory monitoring system by a clinical analysis of the alarms.Study DesignObservational prospective study.Patients25 patients who presented acute respiratory distress syndrome and who were monitored with haemodynamic and respiratory monitoring.MethodsEach minute, a bedside clinical observer analysed alarms from the monitoring according to detection or absence to clinical events. Four situations were defined to statistical descriptive analysis: a) false positive (FP); b) true positive (TP); c) false negative (FN); and d) true negative (TN). True positive alarm which induced consequences on patients care were also analysed.Results15,013 minutes allowed the recordings of 3,665 alarms, 44% from arterial pressure, 17% from SpO2 and 12% from airways maximal pressure. 46% were false positive alarms inducing a noisy pollution. The positive predictive value PPV = TP/(TP + FP) of these alarms were respectively 51% for arterial pressure, 18% for SpO2 and 100% for Paw. Only 5% of true positive alarms induced consequences on patients care.ConclusionThis protocol allowed the evaluation of monitoring efficiency. This kind of evaluation may help to improve monitoring capacity with reducing noisy pollution from false positive alarms.
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