Effekte von Leitlinien

The effect of an algorithm-based sedation guideline on the duration of mechanical ventilation in an Australian intensive care unit.

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The effect of an algorithm-based sedation guideline on the duration of mechanical ventilation in an Australian intensive care unit.

Intensive Care Med. 2006 Oct;32(10):1506-14

Authors: Elliott R, McKinley S, Aitken LM, Hendrikz J

OBJECTIVE: To examine the effect of an algorithm-based sedation guideline developed in a North American intensive care unit (ICU) on the duration of mechanical ventilation of patients in an Australian ICU. DESIGN AND SETTING: The intervention was tested in a pre-intervention, post-intervention comparative investigation in a 14-bed adult intensive care unit. PATIENTS: Adult mechanically ventilated patients were selected consecutively (n[Symbol: see text]=[Symbol: see text]322). The pre-intervention and post-intervention groups were similar except for a higher number of patients with a neurological diagnosis in the pre-intervention group. INTERVENTION: An algorithm-based sedation guideline including a sedation scale was introduced using a multifaceted implementation strategy. MEASUREMENTS AND RESULTS: The median duration of ventilation was 5.6 days in the post-intervention group, compared with 4.8 days for the pre-intervention group (P[Symbol: see text]=[Symbol: see text]0.99). The length of stay was 8.2 days in the post-intervention group versus 7.1 days in the pre-intervention group (P[Symbol: see text]=[Symbol: see text]0.04). There were no statistically significant differences for the other secondary outcomes, including the score on the Experience of Treatment in ICU 7 item questionnaire, number of tracheostomies and number of self-extubations. Records of compliance to recording the sedation score during both phases revealed that patients were slightly more deeply sedated when the guideline was used. CONCLUSIONS: The use of the algorithm-based sedation guideline did not reduce duration of mechanical ventilation in the setting of this study.

PMID: 16896847 [PubMed - in process]

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