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通过多利益相关方参与、共识驱动的过程建立一套儿科重症监护核心质量指标。

Establishing a paediatric critical care core quality measure set using a multistakeholder, consensus-driven process.

作者信息

Schults Jessica A, Charles Karina R, Millar Johnny, Rickard Claire M, Chopra Vineet, Lake Anna, Gibbons Kristen, Long Debbie, Rahiman Sarfaraz, Hutching Katrina, Winderlich Jacinta, Spotswood Naomi E, Johansen Amy, Secombe Paul, Pizimolas Georgina A, Tu Quyen, Waak Michaela, Allen Meredith, McMullan Brendan, Hall Lisa

机构信息

Herston Infectious Diseases Institute, Metro North Hospital and Health Service, Queensland, Australia.

School of Nursing, Midwifery and Social Work, University of Queensland, St Lucia, Queensland, Australia.

出版信息

Crit Care Resusc. 2024 Mar 25;26(2):71-79. doi: 10.1016/j.ccrj.2024.01.002. eCollection 2024 Jun.

Abstract

INTRODUCTION

Monitoring healthcare quality is challenging in paediatric critical care due to measure variability, data collection burden, and uncertainty regarding consumer and clinician priorities.

OBJECTIVE

We sought to establish a core quality measure set that (i) is meaningful to consumers and clinicians and (ii) promotes alignment of measure use and collection across paediatric critical care.

DESIGN

We conducted a multi-stakeholder Delphi study with embedded consumer prioritisation survey. The Delphi involved two surveys, followed by a consensus meeting. Triangulation methods were used to integrate survey findings prior tobefore the consensus meeting. In the consensus panel, broad agreement was reached on a core measure set, and recommendations were made for future measurement directions in paediatric critical care.

SETTING AND PARTICIPANTS

Australian and New Zealand paediatric critical care survivors (aged >18 years) and families were invited to rank measure priorities in an online survey distributed via social media and consumer groups. A concurrent Delphi study was undertaken with paediatric critical care clinicians, policy makers, and a consumer representative.

INTERVENTIONS

None.

MAIN OUTCOME MEASURES

Priorities for quality measures.

RESULTS

Respondents to the consumer survey (n = 117) identified (i) nurse-patient ratios; (ii) visible patient goals; and (iii) long-term follow-up as their quality measure priorities. In the Delphi process, clinicians (Round 1 n = 191; Round 2 n = 117 [61% retention]; Round 3 n = 14) and a consumer representative reached broad agreement on a 51-item (61% of 83 initial measures) core measure set. Clinician priorities were (i) nurse-patient ratio; (ii) staff turnover; and (iii) long term-follow up. Measure feasibility was rated low due to a perceived lack of standardised case definitions or data collection burden. Five recommendations were generated.

CONCLUSIONS

We defined a 51-item core measurement set for paediatric critical care, aligned with clinician and consumer priorities. Next steps are implementation and methodological evaluation in quality programs, and where appropriate, retirement of redundant measures.

摘要

引言

由于测量的变异性、数据收集负担以及消费者和临床医生优先事项的不确定性,在儿科重症监护中监测医疗质量具有挑战性。

目的

我们试图建立一套核心质量指标集,该指标集(i)对消费者和临床医生有意义,并且(ii)促进儿科重症监护中指标使用和收集的一致性。

设计

我们进行了一项多利益相关方德尔菲研究,并嵌入了消费者优先级调查。德尔菲研究包括两次调查,随后是一次共识会议。在共识会议之前,使用三角测量法整合调查结果。在共识小组中,就一套核心指标达成了广泛共识,并为儿科重症监护未来的测量方向提出了建议。

背景和参与者

邀请澳大利亚和新西兰儿科重症监护幸存者(年龄>18岁)及其家人在通过社交媒体和消费者团体分发的在线调查中对指标优先级进行排序。同时对儿科重症监护临床医生、政策制定者和一名消费者代表进行了德尔菲研究。

干预措施

无。

主要观察指标

质量指标的优先级。

结果

消费者调查的受访者(n = 117)将(i)护士与患者的比例;(ii)可见的患者目标;以及(iii)长期随访确定为他们的质量指标优先级。在德尔菲过程中,临床医生(第一轮n = 191;第二轮n = 117 [保留率为61%];第三轮n = 14)和一名消费者代表就一套51项(占83项初始指标的61%)的核心指标集达成了广泛共识。临床医生认为的优先级是(i)护士与患者的比例;(ii)人员流动率;以及(iii)长期随访。由于认为缺乏标准化的病例定义或数据收集负担,指标的可行性被评为较低。提出了五项建议。

结论

我们为儿科重症监护定义了一套51项的核心测量指标集,与临床医生和消费者的优先事项保持一致。下一步是在质量项目中实施和进行方法学评估,并在适当情况下淘汰冗余指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a965/11282349/4491dc7eda74/gr1.jpg

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