追逐黄金时间-改善初始中性粒细胞减少性败血症管理的经验教训。

BMJ quality improvement reports Pub Date : 2017-03-31 eCollection Date: 2017-01-01 DOI:10.1136/bmjquality.u204420.w6531
Caroline Forde, Paula Scullin
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引用次数: 10

摘要

中性粒细胞减少性脓毒症仍然是全身抗癌治疗的时间关键和潜在致命的并发症。在全国范围内继续推广第一剂经验性静脉注射抗生素“从门到针”的目标时间为1小时。基线审计(2011年6月)突出了贝尔法斯特信托的护理不足,只有15%的患者在60分钟内接受抗生素治疗。在信托基金内建立了一个多专业小组,以尝试和启动迫切需要的中性粒细胞减少性败血症识别和初始管理的改进。在过去五年中制定了一些战略。首先,引入了综合护理路径,目前护理人员和医务人员通过急性癌症中心评估区和急诊科,以及出现中性粒细胞减少性败血症的住院患者使用该路径。2012年6月的首次重新审核显示出改善(62%的人达到了1小时目标),但2013年1月的后续审核令人失望(只有50%的人达到了1小时目标)。作为回应,一个新的紧凑,用户友好的护理途径被引入。随后还采取了一系列其他措施。通过简单的基于病房的记录,在每次中性粒细胞减少性败血症发作的初始治疗后完成患者的护理。患者群体指导有利于护士主导的首次抗生素处方和管理。定期举办多学科教育会议和改善获得区域准则的机会也已列为优先事项。从2013年11月开始,一直有超过80%的患者达到了一小时的目标。最近的数据继续令人鼓舞;2016年7月,100%的患者在60分钟内接受了首次剂量,10月,95%的患者接受了首次剂量。在达到60分钟的目标方面已显示出显著的持续改进。这些措施的结合确保中性粒细胞减少性败血症得到考虑,并通过协调的标准化方法快速安全地提供基本临床护理,以避免并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chasing the Golden Hour - Lessons learned from improving initial neutropenic sepsis management.

Chasing the Golden Hour - Lessons learned from improving initial neutropenic sepsis management.

Neutropenic sepsis remains a time critical and potentially fatal complication of systemic anti-cancer therapy. A target 'door to needle' time of one hour for first dose empirical intravenous antibiotics continues to be promoted nationally. A baseline audit (June 2011) highlighted shortfalls in care in the Belfast Trust, with only 15% of patients receiving antibiotics within sixty minutes. A multi-professional group within the Trust was established to try and initiate the improvements in neutropenic sepsis recognition and initial management that were urgently required. A number of strategies have been developed over the last five years. Firstly an integrated care pathway was introduced, which is currently used by nursing and medical staff for patients presenting with suspected neutropenic sepsis, through acute cancer centre assessment areas and emergency departments, as well as inpatients developing neutropenic sepsis. An initial reaudit June 2012 demonstrated improvement (62% meeting 1hour target), but a subsequent audit, January 2013, was disappointing (only 50% meeting 1hour target). In response, a new compact, user-friendly care pathway was introduced. A range of other measures have also been subsequently introduced. Patients' care is continually monitored through simple ward based documentation, completed after initial treatment of each neutropenic sepsis episode. A patient group direction facilitates nurse led prescribing and administration of first dose antibiotics. Regular multidisciplinary education sessions and improved access to regional guidelines have also been prioritised. From November 2013, consistently greater than 80% of patients have met the one hour target. Recent data continues to be encouraging; in July 2016 100% of patients received first doses within sixty minutes, in October 95% of patients. Significant sustained improvements in meeting the sixty minute target have been demonstrated. The combination of measures ensures neutropenic sepsis is considered and basic clinical care delivered quickly and safely, through a co-ordinated standardised approach, to avoid complications.

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