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Feasibility of implementing a multi-component intervention of environmental control in mechanically ventilated ICU patients to improve sleep: A pilot randomized controlled trial 对机械通气ICU患者实施环境控制多组分干预以改善睡眠的可行性:一项随机对照试验
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-30 DOI: 10.1016/j.iccn.2026.104349
Vanessa Oviedo , Leyla Alegría , Douglas Leonard , Rodrigo Cádiz , Pablo Brockmann , Paula Repetto , Mario Henríquez , Gonzalo Labarca , Margarita Carrasco , Ana Moya , Idalid Rojas , Macarena Amthauer , Hugo Vidal , María Paz Carrera , Jan Bakker

Objectives

To evaluate the feasibility of implementing a multi-component intervention in the ICU to promote sleep in critically ill patients.

Trial design

A prospective, two-parallel-group, unblinded, pilot randomized controlled trial.

Methods

Adult patients ventilated for at least 48 h with no or superficial sedation in the past 24 h were recruited. They were randomized to receive a multi-component ICU environmental control intervention (dynamic light therapy, auditory masking, and rationalization of nighttime care) or standard care. A family member of each participant consented to the study.

Main outcome measures

The primary outcomes were the feasibility of enrolling and retaining participants and the fidelity of the intervention. Secondary outcomes were sleep quantity (assessed by polysomnography and actigraphy) and sleep quality (assessed by Richards-Campbell Sleep Questionnaire), the prevalence of delirium at day three post-randomization, and neuropsychological impairment at six months post-ICU discharge.

Setting

An intensive care unit in a tertiary care teaching hospital in Santiago, Chile.

Results

122 patients were screened; 17 were randomized, 9 to intervention and 8 to control. 78% (7) and 100% (8) stayed in ICU until day three. All 8 in the intervention group received the full intervention until ICU discharge. The enrollment rate was 94%. The 6-month follow-up rate was 35%, as some patients died. All participants who completed the study nights expressed very high satisfaction.

Conclusions

This pilot study demonstrates the feasibility and acceptability of the intervention and informs methodological refinements for a future trial.

Implications for clinical practice

Implementing a multi-component environmental control intervention in intensive care units could improve short- and long-term outcomes in ventilated patients; however, further high-quality efficacy trials are required.
目的探讨在重症监护病房实施多组分干预以促进危重患者睡眠的可行性。试验设计一项前瞻性、双平行组、非盲、先导随机对照试验。方法选取过去24 h内未使用或未使用表面镇静且通气至少48 h的成人患者。他们随机接受多组分ICU环境控制干预(动态光疗、听觉掩蔽和夜间护理合理化)或标准护理。每位参与者都有一名家庭成员同意参加这项研究。主要结局指标主要结局指标是招募和保留参与者的可行性以及干预的保真度。次要结果是睡眠量(通过多导睡眠图和活动图评估)和睡眠质量(通过Richards-Campbell睡眠问卷评估),随机分组后第三天谵妄的患病率,以及icu出院后6个月的神经心理损伤。背景:智利圣地亚哥一家三级护理教学医院的重症监护室。结果共筛选122例患者;17例随机化,干预组9例,对照组8例。78%(7人)和100%(8人)在ICU待到第3天。干预组8例患者均给予全程干预至ICU出院。入学率为94%。6个月随访率为35%,部分患者死亡。所有完成夜间学习的参与者都表达了很高的满意度。该初步研究证明了干预的可行性和可接受性,并为未来试验的方法改进提供了信息。在重症监护病房实施多组分环境控制干预可以改善通气患者的短期和长期预后;然而,需要进一步的高质量疗效试验。
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引用次数: 0
Patient and family-centered interdisciplinary rounds and patient satisfaction: A controlled intervention study 以患者和家庭为中心的跨学科查房与患者满意度:一项对照干预研究
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-30 DOI: 10.1016/j.iccn.2026.104347
Brigitte S. Cypress, Rida Gharzeddine

Objectives

Interdisciplinary rounds are a core component of care delivery in intensive care units (ICUs), supporting communication, coordination, and shared decision-making. Although patient- and family-centered interdisciplinary rounds (PFCC-IR) are recommended, evidence linking PFCC-IR to patients’ satisfaction with nursing care remains limited, as prior research has focused largely on family perceptions. This study evaluated the effect of family engagement during ICU interdisciplinary rounds on patient satisfaction with nursing care.

Methods

A quasi-experimental, two-group pre–post design was conducted in adult ICUs. Patients in the intervention group had a family member participate in interdisciplinary rounds, whereas control patients received standard care without family involvement. Using convenience sampling, 150 patients were enrolled (75 per group). Satisfaction was measured pre- and post-intervention using the Patient Satisfaction with Nursing Care Quality Questionnaire, which demonstrated high internal consistency. Linear mixed-effects regression examined group differences over time, adjusting for age, gender, marital status, and number of rounds attended.

Results

Participants had a mean age of 63.4 years; 41% were male, and 41% were married. Satisfaction scores changed minimally in the control group (mean difference = 0.76, p = 0.20). In contrast, the intervention group demonstrated significant improvement following family engagement during rounds (mean difference = –47.4, p < 0.001). Linear mixed-effects analysis confirmed a significant treatment effect (time × group interaction = –47.43, p < 0.001).

Conclusions

Engaging family members during ICU interdisciplinary rounds was associated with significantly improved patient satisfaction with nursing care. These findings support the Society for Critical Care Medicine’s clinical practice guidelines recommending that families be offered the option to be present and engaged during ICU rounds.

Implications for Practice

Integrating structured family participation into ICU interdisciplinary rounds is a feasible, nursing-led strategy to enhance communication and patient-centered care. Institutions should implement clear policies and workflows to support family engagement.
跨学科查房是重症监护病房(icu)护理服务的核心组成部分,支持沟通、协调和共同决策。虽然推荐以患者和家庭为中心的跨学科查房(PFCC-IR),但PFCC-IR与患者护理满意度之间的联系证据仍然有限,因为先前的研究主要集中在家庭观念上。本研究评估ICU跨学科查房时家庭参与对患者护理满意度的影响。方法对成人重症监护病房进行准实验、两组前后设计。干预组患者有一名家庭成员参与跨学科查房,而对照组患者则接受没有家庭参与的标准治疗。采用方便抽样,150例患者入组(每组75例)。在干预前和干预后分别采用患者护理质量满意度问卷进行满意度测量,结果具有较高的内部一致性。线性混合效应回归检验了各组间随时间的差异,调整了年龄、性别、婚姻状况和就诊次数。结果参与者平均年龄63.4岁;其中41%为男性,41%为已婚。对照组满意度评分变化最小(平均差异= 0.76,p = 0.20)。相比之下,干预组在轮次家庭参与后表现出显著改善(平均差异= -47.4,p < 0.001)。线性混合效应分析证实治疗效果显著(时间×组交互作用= -47.43,p < 0.001)。结论在ICU跨学科查房时让家属参与可显著提高患者对护理的满意度。这些发现支持了重症监护医学协会的临床实践指南,建议在重症监护病房查房时,为家属提供在场和参与的选择。将有组织的家庭参与纳入ICU跨学科查房是一种可行的,以护理为主导的策略,以加强沟通和以患者为中心的护理。各机构应实施明确的政策和工作流程,以支持家庭参与。
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引用次数: 0
Adolescent relatives’ experiences and perceptions of everyday life when a family member is critically ill and admitted to an ICU and in the aftermath: A qualitative study 青少年亲属的经验和日常生活的看法,当一个家庭成员是重症监护病房和在后果:一项定性研究
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-23 DOI: 10.1016/j.iccn.2026.104333
Mathilde Elsa Christensen , Gro Frivold , Gudrun Elin Rohde

Aims

This study explored the experiences and perceptions of adolescents who were relatives of intensive care unit (ICU) patients, focusing on their everyday lives during and after the ICU stay.

Design

Inductive descriptive qualitative study.

Methods

Semi-structured, in-depth interviews were conducted and analysed using reflexive thematic analysis (RTA).

Findings

Sixteen adolescents as relatives of ICU patients in Norway were included. Three themes were identified: Navigating adolescence independently during critical illness, Relational bonds and A new everyday life. Eight sub-themes identified: Feeling isolated, need for support from knowledgeable adults, striving for normalcy, avoid being a burden, loyalty to their family, adaptation in roles and changed relations, experiencing mental and physical challenges and existential experiences.

Conclusions

Adolescent relatives of critically ill patients experienced substantial uncertainty and distress, with their attention persistently focused on the critically ill family member. Their lives were significantly altered, resulting in unpredictability. Some adolescents reported personal growth in the aftermath. The adolescents expressed a need for a structured support programme.

Implications for clinical practice

The adolescents experienced substantial disruption in their everyday lives and often lacked systematic support when a family member was admitted to an ICU. The findings suggest that health care professionals (HCPs), both in the ICU and school health service, should collaborate to offer targeted support to adolescents who are relatives of ICU patients.
目的本研究探讨重症监护病房(ICU)患者亲属的青少年的经历和看法,重点关注他们在ICU住院期间和之后的日常生活。设计归纳描述性定性研究。方法采用半结构化、深度访谈法,采用自反性主题分析(RTA)进行分析。结果纳入挪威ICU患者亲属的16名青少年。研究确定了三个主题:在重大疾病中独立度过青春期、关系纽带和新的日常生活。确定了八个副主题:感到孤立、需要有知识的成年人的支持、努力恢复正常、避免成为负担、忠于家庭、适应角色和改变的关系、经历精神和身体挑战以及存在体验。结论危重患者青少年亲属存在大量的不确定性和痛苦,其注意力持续集中在危重患者家属身上。他们的生活发生了巨大的变化,导致了不可预测性。一些青少年报告说,在事件发生后,他们的个人成长了。青少年表示需要一个有组织的支助方案。对临床实践的启示青少年在日常生活中经历了实质性的破坏,当家庭成员被送入ICU时,往往缺乏系统的支持。研究结果提示,ICU和学校卫生服务部门的卫生保健专业人员(HCPs)应该合作,为ICU患者亲属的青少年提供有针对性的支持。
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引用次数: 0
A matter of perspective: How divergent professional logics shape perceptions of appropriate care in the ICU 观点问题:不同的专业逻辑如何塑造ICU中适当护理的观念。
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-20 DOI: 10.1016/j.iccn.2026.104339
Anna-Henrikje Seidlein
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引用次数: 0
Anticipatory guidance for parents following paediatric intensive care: a scoping review and environmental scan of recovery-focused resources 对儿童重症监护后父母的预期指导:以恢复为重点的资源的范围审查和环境扫描。
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-19 DOI: 10.1016/j.iccn.2025.104332
Leigh Dunn , Suzanne Williams , Debbie Long

Objectives

To map and critically appraise anticipatory guidance interventions and resources for parents following PICU discharge, examine how they address recovery challenges, and identify gaps to inform parent-centred resource development.

Methods

Database search across EBSCO (MEDLINE, CINAHL, PsychINFO), Embase, Scopus, Web of Science, and Cochrane Library for studies published January 2000-June 2025. Environmental scan via targeted and Google searches. Five tools assessed delivery, understandability, actionability, quality, and readability.

Results

Of 1752 records, four studies and nine digital resources met inclusion criteria (n = 271 parents). Formats included phone calls, brochures, in-person conversations, plus websites, webpages, downloadable content, and videos, from university children’s hospitals (n = 10), and organisations (n = 3) across the US (n = 9), UK (n = 3), and Australia (n = 1). Three key findings emerged: (1) support for how parents’ access, understand, and use information was inconsistent; (2) resources prioritised functional (reading/comprehension), over interactive (communication, application) or critical health literacy (evaluation, advocacy); (3) system-level health literacy strategies were limited.

Conclusion

There is an urgent need to strengthen anticipatory guidance by embedding health literacy principles across design and delivery. This includes addressing organisational barriers to access and equity through co-design, plain language, and culturally responsive approaches. Beyond information provision, a deliberate focus on capability building can empower parents as active partners in care, ultimately improving outcomes for children and families.

Implications for clinical practice

Anticipatory guidance following PICU discharge must move beyond information provision toward capacity building that supports parents to apply, evaluate, and act on information. Embedding health literacy principles − plain language, readability testing, co-design, and cultural responsiveness − into resource development is critical to ensure accessibility and equity. Clinician education and integration into routine workflows are equally important to optimise resource impact. A universal precautions approach offers a practical strategy for health services to ensure all families, regardless of literacy level, receive clear, actionable, and supportive guidance.
目的:绘制和批判性评估PICU出院后父母的预期指导干预措施和资源,检查它们如何应对康复挑战,并确定差距,为以父母为中心的资源开发提供信息。方法:检索EBSCO (MEDLINE, CINAHL, PsychINFO), Embase, Scopus, Web of Science和Cochrane Library数据库,检索2000年1月至2025年6月发表的研究。环境扫描通过目标和谷歌搜索。五个工具评估交付、可理解性、可操作性、质量和可读性。结果:在1752份记录中,有4项研究和9个数字资源符合纳入标准(n = 271名家长)。格式包括电话、宣传册、面对面谈话、网站、网页、可下载内容和视频,来自美国(n = 9)、英国(n = 3)和澳大利亚(n = 1)的大学儿童医院(n = 10)和组织(n = 3)。主要发现有三个:(1)支持家长获取、理解和使用信息的方式不一致;(2)资源优先于功能性(阅读/理解),而不是互动性(沟通、应用)或关键的健康素养(评估、倡导);(3)系统级卫生素养战略有限。结论:迫切需要通过在设计和交付过程中嵌入卫生素养原则来加强预期指导。这包括通过共同设计、通俗易懂的语言和文化响应方法来解决组织在获取和公平方面的障碍。除了提供信息之外,刻意注重能力建设可以使父母成为护理的积极伙伴,最终改善儿童和家庭的结果。对临床实践的启示:PICU出院后的预期指导必须从信息提供转向能力建设,支持家长应用、评估和根据信息采取行动。将卫生扫盲原则——通俗易懂的语言、可读性测试、共同设计和文化响应性——纳入资源开发,对于确保可及性和公平性至关重要。临床医生教育和融入日常工作流程对于优化资源影响同样重要。普遍预防措施为卫生服务提供了一项切实可行的战略,以确保所有家庭,无论其文化水平如何,都能获得明确、可操作和支持性的指导。
{"title":"Anticipatory guidance for parents following paediatric intensive care: a scoping review and environmental scan of recovery-focused resources","authors":"Leigh Dunn ,&nbsp;Suzanne Williams ,&nbsp;Debbie Long","doi":"10.1016/j.iccn.2025.104332","DOIUrl":"10.1016/j.iccn.2025.104332","url":null,"abstract":"<div><h3>Objectives</h3><div>To map and critically appraise anticipatory guidance interventions and resources for parents following PICU discharge, examine how they address recovery challenges, and identify gaps to inform parent-centred resource development.</div></div><div><h3>Methods</h3><div>Database search across EBSCO (MEDLINE, CINAHL, PsychINFO), Embase, Scopus, Web of Science, and Cochrane Library for studies published January 2000-June 2025. Environmental scan via targeted and Google searches. Five tools assessed delivery, understandability, actionability, quality, and readability.</div></div><div><h3>Results</h3><div>Of 1752 records, four studies and nine digital resources met inclusion criteria (n = 271 parents). Formats included phone calls, brochures, in-person conversations, plus websites, webpages, downloadable content, and videos, from university children’s hospitals (n = 10), and organisations (n = 3) across the US (n = 9), UK (n = 3), and Australia (n = 1). Three key findings emerged: (1) support for how parents’ access, understand, and use information was inconsistent; (2) resources prioritised functional (reading/comprehension), over interactive (communication, application) or critical health literacy (evaluation, advocacy); (3) system-level health literacy strategies were limited.</div></div><div><h3>Conclusion</h3><div>There is an urgent need to strengthen anticipatory guidance by embedding health literacy principles across design and delivery. This includes addressing organisational barriers to access and equity through co-design, plain language, and culturally responsive approaches. Beyond information provision, a deliberate focus on capability building can empower parents as active partners in care, ultimately improving outcomes for children and families.</div></div><div><h3>Implications for clinical practice</h3><div>Anticipatory guidance following PICU discharge must move beyond information provision toward capacity building that supports parents to apply, evaluate, and act on information. Embedding health literacy principles − plain language, readability testing, co-design, and cultural responsiveness − into resource development is critical to ensure accessibility and equity. Clinician education and integration into routine workflows are equally important to optimise resource impact. A universal precautions approach offers a practical strategy for health services to ensure all families, regardless of literacy level, receive clear, actionable, and supportive guidance.</div></div>","PeriodicalId":51322,"journal":{"name":"Intensive and Critical Care Nursing","volume":"93 ","pages":"Article 104332"},"PeriodicalIF":4.7,"publicationDate":"2026-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146014136","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Moral distress: The unmeasured catalyst in preventing catheter-associated bloodstream infections in neonatal ICUs − Letter on Berdida et al. 道德困扰:预防新生儿重症监护病房导管相关血流感染的未测催化剂——Berdida等人的信。
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-19 DOI: 10.1016/j.iccn.2026.104341
Peiyan Lin, Yuliu Huang
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引用次数: 0
Early enteral nutritional support and clinical outcomes in critically ill children: A scoping review 危重儿童早期肠内营养支持和临床结果:范围综述。
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-19 DOI: 10.1016/j.iccn.2026.104336
Marina Maffeo , Gabriele Caggianelli , Emanuele Buccione , Valentina Vanzi , Daniele Ciofi , Mirco Gregorini , Maurizio Zega , Jacopo Fiorini

Background and aims

Pediatric malnutrition, is defined as an imbalance between nutrient intake and requirements leading to cumulative energy, protein, or micronutrient deficits, is highly prevalent among critically ill children and negatively affects growth and recovery. Early enteral nutrition (EEN) is increasingly recognized as a key strategy to prevent or address malnutrition in pediatric intensive care units (PICUs). Although emerging evidence suggests that EEN improves clinical outcomes, uncertainty persists regarding its feasibility and impact in this population. This scoping review aimed to map existing evidence on the use of EEN in critically ill children, evaluate its effects on key clinical outcomes including mechanical ventilation duration, length of stay, and infection risk; and identify barriers and facilitators to its implementation in pediatric intensive care settings.

Methods

A scoping review was conducted following Joanna Briggs Institute methodology and PRISMA-ScR guidelines. Searches were performed in PubMed, Embase, Scopus, CINAHL, and the Cochrane Library. Studies were eligible if they involved children aged 1 month to 18 years and initiated enteral nutrition within 48 h of PICU admission. Keywords included child, critical illness, enteral nutrition, intensive care units, and pediatrics. Studies in English or Italian were included without date restrictions.

Results

Sixteen thousand seven hundred ninety-nine records were identified; 15,556 were screened after duplicates were removed, and 14 studies met inclusion criteria (USA n = 6; Asia n = 4; Africa n = 3; Europe n = 1). Most were cohort studies, with one randomized trial. EEN was consistently associated with shorter mechanical ventilation duration (5.86 ± 3.63 vs 11.96 ± 9.17 days, p = 0.002), reduced PICU and hospital length of stay (4 vs 11.5 days, p < 0.001), and lower infection rates (16.7 % vs 41.1 %, p = 0.001). Barriers to EEN included hemodynamic instability, gastrointestinal intolerance, and procedural interruptions, while facilitators included multidisciplinary teamwork, nurse-led feeding protocols, and standardized nutritional guidelines.

Conclusion

EEN initiated within 24–48 h was generally associated with favorable clinical outcomes; however, evidence on feasibility and safety remains limited and heterogeneous. Strengthening nursing autonomy and implementing standardized feeding pathways may enhance timely nutrition delivery and support recovery in pediatric intensive care.

Implications for clinical practice

Pediatric intensive care nurses play a pivotal role in initiating and monitoring EEN. Empowering nurses through evidence-based feeding protocols and multidisciplinary education can promote timely nutrition delivery and improve recovery in critically ill children.
背景和目的:儿童营养不良被定义为营养摄入与需求之间的不平衡,导致累积的能量、蛋白质或微量营养素缺乏,在危重儿童中非常普遍,并对生长和恢复产生负面影响。早期肠内营养(EEN)越来越被认为是预防或解决儿童重症监护病房(picu)营养不良的关键策略。尽管越来越多的证据表明EEN可以改善临床结果,但其在该人群中的可行性和影响仍然存在不确定性。本综述旨在整理危重儿童使用EEN的现有证据,评估其对关键临床结果的影响,包括机械通气时间、住院时间和感染风险;并确定在儿科重症监护环境中实施的障碍和促进因素。方法:根据Joanna Briggs研究所的方法和PRISMA-ScR指南进行范围审查。在PubMed、Embase、Scopus、CINAHL和Cochrane Library中进行检索。如果研究涉及1个月至18岁的儿童,并在PICU入院后48小时内开始肠内营养,则研究符合条件。关键词:儿童,危重疾病,肠内营养,重症监护病房,儿科学。包括英语或意大利语的研究,没有日期限制。结果:共鉴定记录16799条;剔除重复项后筛选了15,556项研究,其中14项研究符合纳入标准(美国n = 6;亚洲n = 4;非洲n = 3;欧洲n = 1)。大多数是队列研究,其中有一项随机试验。EEN与较短的机械通气时间(5.86±3.63天vs 11.96±9.17天,p = 0.002)、减少PICU和住院时间(4天vs 11.5天,p)一致相关。结论:在24-48小时内启动EEN通常与良好的临床结果相关;然而,关于可行性和安全性的证据仍然有限且存在异质性。加强护理自主权和实施标准化喂养途径可提高儿科重症监护及时提供营养和支持康复。对临床实践的启示:儿科重症监护护士在启动和监测EEN方面发挥着关键作用。通过循证喂养方案和多学科教育赋予护士权力,可以促进及时提供营养,改善危重儿童的康复。
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引用次数: 0
Causes, characteristics and improvement strategies for delayed interventions during paediatric deterioration: A mixed methods systematic review 儿童病情恶化时延迟干预的原因、特点和改进策略:一项混合方法系统综述。
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-19 DOI: 10.1016/j.iccn.2025.104330
Shannon Cresham Fox , Takawira C. Marufu , Emma Popejoy , Nicola Taylor , Damien Roland , Joseph C. Manning

Background

Children are susceptible to deterioration due to compensatory mechanisms. Timely recognition and intervention are strongly associated with improved clinical outcomes, whereas delays elevate mortality risk. Failure to rescue (FtR), the inability to prevent death following deterioration, represents a critical safety concern, yet contributory factors and contextual characteristics remain inadequately synthesised.

Aim

Identify and evaluate causes, characteristics and improvement strategies associated with delayed intervention during paediatric clinical deterioration in hospitalised children.

Methods

A mixed-methods systematic review of five databases was conducted including studies on hospitalised children (0–18 years) reporting outcomes related to FtR (e.g. mortality), published after 2000. Rigour was ensured through PROSPERO registration (CRD420250651864) and appraisal checklists. Data were analysed using a convergent segregated approach.

Results

Fifty-two studies included 820,000 hospitalised children and 4.4 million clinical events were synthesised. Qualitative and quantitative findings resulted in three themes: recognition, escalation and response, with qualitative findings presenting insight into barriers associated with each stage (including unclear escalation pathways and training gaps). Whilst quantitative findings reported prevalence of delayed recognition, escalation and response with pervasive organisational factors contributing to delays (e.g. staffing). Younger children and children with medical complexity (CMC) were at increased risk, and global majority populations were disproportionately affected. Integrated synthesis showed delays stem from individual, organisational, and systemic factors, while experienced nurses play a critical role in timely intervention.

Conclusion

Individual, organisational and systemic factors contribute to delayed intervention. CMC and global majority populations were disproportionately affected. Findings highlight critical points of delay. Reporting participant characteristics (e.g. ethnicity, medical complexity) is essential to understand their impact upon deterioration pathways.

Implications for clinical practice

Nurses are pivotal in recognising and responding to deterioration, and should recognise high-risk groups. Awareness should translate into advocacy for early intervention.
背景:由于代偿机制的存在,儿童易发生神经退化。及时识别和干预与改善临床结果密切相关,而延迟则会增加死亡风险。抢救失败(FtR),即无法预防病情恶化后的死亡,是一个严重的安全问题,但促成因素和背景特征仍未得到充分综合。目的:识别和评估住院儿童临床恶化期间延迟干预的原因、特征和改善策略。方法:对5个数据库进行混合方法系统评价,包括2000年以后发表的关于报告FtR相关结果(如死亡率)的住院儿童(0-18岁)的研究。通过PROSPERO注册(CRD420250651864)和评估清单确保了严谨性。数据分析使用收敛分离的方法。结果:52项研究包括82万住院儿童和440万临床事件。定性和定量研究结果产生了三个主题:认识、升级和反应,定性研究结果对每个阶段相关的障碍(包括不明确的升级途径和培训差距)提出了见解。同时,定量调查结果报告了延迟识别、升级和反应的普遍性,以及导致延迟的普遍组织因素(例如人员配备)。年龄较小的儿童和患有医疗复杂性(CMC)的儿童的风险增加,全球大多数人口受到不成比例的影响。综合综合显示延迟源于个人,组织和系统因素,而经验丰富的护士在及时干预中发挥关键作用。结论:个体因素、组织因素和系统因素导致延迟干预。CMC和全球大多数人口受到不成比例的影响。研究结果突出了延迟的关键点。报告参与者特征(如种族、医疗复杂性)对于了解其对恶化途径的影响至关重要。对临床实践的启示:护士在识别和应对恶化是关键的,应该认识到高危人群。认识应转化为倡导早期干预。
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引用次数: 0
Effect of complementary therapies on chronic obstructive pulmonary disease patient outcomes treated with noninvasive ventilation: A systematic review 辅助疗法对无创通气治疗慢性阻塞性肺疾病患者预后的影响:一项系统综述。
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-17 DOI: 10.1016/j.iccn.2026.104340
Dilara Ülke Çelik, Meral Gün

Background

COPD patients receiving noninvasive ventilation (NIV) face many physiological and psychosocial problems. The impact of complementary therapies on NIV adherence and symptom management in COPD patients is not sufficiently addressed.

Objective

This systematic review was conducted to examine the effectiveness of complementary therapies used in COPD patients receiving NIV on clinical symptoms and health outcomes.

Methods

A systematic review was designed based on PRISMA-P (Preferred Reporting Items for Systematic review and Meta-Analysis Protocols) criteria. The literature search was conducted in the “PubMed, Cochrane, Scopus, Web of Science, Google Scholar” databases. Studies were selected by determining inclusion and exclusion criteria according to the PICOT method. Studies were evaluated using the Joanna Briggs Institute (JBI) critical assessment lists.

Results

Five randomized controlled trials were included in the systematic review, which included a total of 338 COPD patients receiving NIV. Most studies have found that complementary therapies significantly reduce anxiety and dyspnea levels. Significant improvements were observed in physical capacity and quality of life.

Conclusions

Complementary therapies may offer potential benefits for clinical symptoms and health outcomes in patients receiving NIV, including anxiety, dyspnea, physical capacity and quality of life. However, the findings are limited by substantial heterogeneity and methodological shortcomings among the included studies. Well-designed, controlled clinical trials are needed to provide more definitive evidence regarding the effects of complementary therapies in this population.

Implications for Clinical Practice

The current evidence remains insufficient to support the routine incorporation of complementary therapies into critical care practice for patients with COPD receiving NIV. Further high-quality studies are required to guide nursing practice and support the integration of complementary therapies into holistic care.
背景:接受无创通气(NIV)的COPD患者面临许多生理和社会心理问题。补充疗法对COPD患者依从性和症状管理的影响尚未得到充分解决。目的:本系统综述旨在探讨辅助疗法对COPD患者临床症状和健康结局的影响。方法:根据PRISMA-P(系统评价和荟萃分析方案的首选报告项目)标准设计系统评价。文献检索在“PubMed, Cochrane, Scopus, Web of Science, b谷歌Scholar”数据库中进行。根据PICOT方法确定纳入和排除标准来选择研究。研究使用乔安娜布里格斯研究所(JBI)的关键评估清单进行评估。结果:系统评价纳入5项随机对照试验,共纳入338例接受NIV治疗的COPD患者。大多数研究发现,辅助疗法可以显著降低焦虑和呼吸困难水平。在身体能力和生活质量方面观察到显著的改善。结论:辅助疗法可能对接受NIV的患者的临床症状和健康结果有潜在的益处,包括焦虑、呼吸困难、身体能力和生活质量。然而,研究结果受到纳入研究的实质性异质性和方法学缺陷的限制。需要精心设计的对照临床试验,以提供关于补充疗法在这一人群中的效果的更明确的证据。对临床实践的影响:目前的证据仍然不足以支持将补充疗法常规纳入接受NIV的COPD患者的重症监护实践。需要进一步的高质量研究来指导护理实践,并支持将补充疗法整合到整体护理中。
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引用次数: 0
Complex cases and coordination: Reports from organ donation specialists in Canada 复杂病例和协调:来自加拿大器官捐赠专家的报告。
IF 4.7 2区 医学 Q1 NURSING Pub Date : 2026-01-17 DOI: 10.1016/j.iccn.2026.104335
Amina Silva , Ken Lotherington , Sonny Dhanani , Julia Luvizutto , Vanessa Silva e Silva

Objectives

To explore Organ and Tissue Donation Coordinator nurses’ experiences and perceptions of their most challenging and complex cases, with a focus on emotional, ethical, and procedural factors.

Methods

Qualitative descriptive study where data were collected using a semi-structured interview guide and analyzed using a thematic analysis approach.

Findings

29 coordinators were interviewed from April 2022 to February 2023 across all Canadian provinces. Most coordinators have been in their role for 6.9 years, and have experience in critical care. Two overarching themes captured the complexity of coordinators’ experiences: (1) Donation Type, encompassing donation after death determination by circulatory criteria and specific donor circumstances, and (2) Pediatric versus Adult Contexts, highlighting contrasts in family, patient, recipient, and team dynamics. Donation after death determination by circulation criteria cases were characterized by procedural pressure due to sensitivity. In contrast, specific donor types, such as patients undergoing medical assistance in dying, intensified emotional and ethical strain through personal connections with donors. Pediatric cases further amplified emotional complexity, extending family interactions and deepening the search for meaning in care.

Conclusion

Our findings highlighted that coordinators face significant challenges in complex organ and tissue donation cases and there is a current need for targeted interventions to psychologically enhance support systems and improve the coordination of deceased organ donation.

Implications for clinical practice

Understanding the multifaceted challenges coordinators encounter in complex donation contexts in critical care can inform future training development, psychosocial support, and interdisciplinary communication strategies, thereby improving the overall quality of care provided during donation processes.
目的:探讨器官和组织捐赠协调员护士对最具挑战性和最复杂的病例的经验和看法,重点是情感、道德和程序因素。方法:定性描述性研究,使用半结构化访谈指南收集数据,并使用主题分析方法进行分析。调查结果:从2022年4月到2023年2月,加拿大所有省份的29名协调员接受了采访。大多数协调员已在其岗位上工作了6.9年,并具有重症监护经验。两个主要主题反映了协调员经验的复杂性:(1)捐赠类型,包括根据循环标准和特定捐赠情况确定的死后捐赠;(2)儿科与成人背景,突出家庭、患者、接受者和团队动态的对比。根据循环标准确定的死亡后捐赠病例的特点是由于敏感性而存在程序压力。相比之下,特定类型的捐赠者,如接受医疗援助的临终病人,通过与捐赠者的个人联系,加剧了情感和道德上的紧张。儿科病例进一步放大了情感复杂性,扩大了家庭互动,加深了对护理意义的探索。结论:我们的研究结果强调,协调人员在复杂的器官和组织捐赠病例中面临着重大挑战,目前需要有针对性的干预措施,从心理上加强支持系统,改善死者器官捐赠的协调。对临床实践的启示:了解协调员在复杂的重症监护捐赠环境中遇到的多方面挑战,可以为未来的培训发展、社会心理支持和跨学科沟通策略提供信息,从而提高捐赠过程中提供的整体护理质量。
{"title":"Complex cases and coordination: Reports from organ donation specialists in Canada","authors":"Amina Silva ,&nbsp;Ken Lotherington ,&nbsp;Sonny Dhanani ,&nbsp;Julia Luvizutto ,&nbsp;Vanessa Silva e Silva","doi":"10.1016/j.iccn.2026.104335","DOIUrl":"10.1016/j.iccn.2026.104335","url":null,"abstract":"<div><h3>Objectives</h3><div>To explore Organ and Tissue Donation Coordinator nurses’ experiences and perceptions of their most challenging and complex cases, with a focus on emotional, ethical, and procedural factors.</div></div><div><h3>Methods</h3><div>Qualitative descriptive study where data were collected using a semi-structured interview guide and analyzed using a thematic analysis approach.</div></div><div><h3>Findings</h3><div>29 coordinators were interviewed from April 2022 to February 2023 across all Canadian provinces. Most coordinators have been in their role for 6.9 years, and have experience in critical care. Two overarching themes captured the complexity of coordinators’ experiences: (1) Donation Type, encompassing donation after death determination by circulatory criteria and specific donor circumstances, and (2) Pediatric versus Adult Contexts, highlighting contrasts in family, patient, recipient, and team dynamics. Donation after death determination by circulation criteria cases were characterized by procedural pressure due to sensitivity. In contrast, specific donor types, such as patients undergoing medical assistance in dying, intensified emotional and ethical strain through personal connections with donors. Pediatric cases further amplified emotional complexity, extending family interactions and deepening the search for meaning in care.</div></div><div><h3>Conclusion</h3><div>Our findings highlighted that coordinators face significant challenges in complex organ and tissue donation cases and there is a current need for targeted interventions to psychologically enhance support systems and improve the coordination of deceased organ donation.</div></div><div><h3>Implications for clinical practice</h3><div>Understanding the multifaceted challenges coordinators encounter in complex donation contexts in critical care can inform future training development, psychosocial support, and interdisciplinary communication strategies, thereby improving the overall quality of care provided during donation processes.</div></div>","PeriodicalId":51322,"journal":{"name":"Intensive and Critical Care Nursing","volume":"93 ","pages":"Article 104335"},"PeriodicalIF":4.7,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146000153","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Intensive and Critical Care Nursing
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