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Psychosocial adjustment changes and related factors in young and middle-aged patients with first-episode acute myocardial infarction: a longitudinal study 首次急性心肌梗死中青年患者的社会心理适应变化及相关因素:一项纵向研究
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-05-02 DOI: 10.1093/eurjcn/zvae065
Xin-yi Zhou, Qi-qi Ke, Wei-yu Qiu, Yao-xia Li, Qin-yang Wu, Qiu-yun Ye, Qiao-hong Yang
Aims This study aimed to explore the change trend and group heterogeneity of psychosocial adjustment level and to determine its influencing factors among young and middle-aged patients with first-episode acute myocardial infarction (AMI). Methods and results The Psychosocial Adjustment Scale of Illness was used to assess the psychosocial adjustment level of the patients at 1, 3, and 6 months after discharge, respectively. Data were analyzed using Pearson correlation analysis, generalized estimating equations, and growth mixed models. A total of 233 patients were included, and their psychosocial adjustment scores at the three-time points were 57.18 ± 15.50, 36.17 ± 15.02, and 24.22 ± 12.98, respectively. The trajectories of changes in patients’ psychosocial adjustment levels were divided into three latent categories: moderate adjustment improvement group (72.5%), low adjustment improvement group (16.3%), and persistent maladjustment group (11.2%). Among them, predictors of the persistent maladjustment group included no spouse, low monthly family income per capita, normal body mass index, never smoking, never exercising, combined with hyperlipidemia, low social support, submission coping, and high perceived stress. Conclusions The psychosocial adjustment level of young and middle-aged patients with first-episode AMI showed an upward trend within 6 months after discharge, and there was group heterogeneity in the change trajectory of psychosocial adjustment level. It is suggested that a multi-center, large-sample longitudinal study should be carried out in the future, and the time of follow-up investigation should be extended to further clarify the change trajectory and influencing factors of psychosocial adjustment of patients with different subtypes, to provide the theoretical basis for formulating targeted intervention programs.
目的 本研究旨在探讨中青年首发急性心肌梗死(AMI)患者社会心理适应水平的变化趋势和群体异质性,并确定其影响因素。方法和结果 采用疾病社会心理适应量表分别评估患者出院后 1 个月、3 个月和 6 个月的社会心理适应水平。数据采用皮尔逊相关分析、广义估计方程和增长混合模型进行分析。共纳入了 233 名患者,他们在三个时间点的社会心理适应评分分别为(57.18±15.50)分、(36.17±15.02)分和(24.22±12.98)分。患者社会心理适应水平的变化轨迹被分为三个潜在类别:中度适应改善组(72.5%)、低度适应改善组(16.3%)和持续适应不良组(11.2%)。其中,持续适应不良组的预测因素包括无配偶、家庭人均月收入低、体重指数正常、从不吸烟、从不运动、合并高脂血症、社会支持低、屈从应对和高感知压力。结论 首次发病的中青年 AMI 患者的社会心理适应水平在出院后 6 个月内呈上升趋势,社会心理适应水平的变化轨迹存在群体异质性。建议今后开展多中心、大样本的纵向研究,延长随访调查时间,进一步明确不同亚型患者社会心理适应的变化轨迹和影响因素,为制定有针对性的干预方案提供理论依据。
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引用次数: 0
Device-specific quality of life: Results from the ATLAS trial—Avoid Transvenous Leads in Appropriate Subjects 设备特异性生活质量:ATLAS 试验--在适当受试者中避免使用经静脉导联--的结果
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-29 DOI: 10.1093/eurjcn/zvae067
Sandra L Carroll, Blandine Mondésert, Andrew D Krahn, Jamil G Bashir, Kathryn Fisher, Kalpana Nair, Jeff S Healey
Aim Patient reported outcomes (PROs) provide important insights into patients’ acceptance of their medical devices. ATLAS, a randomized, multi-center, open-label clinical trial, recently reported fewer perioperative complications in S-ICD compared to TV-ICD patients. This study reports PROs, including device-specific and generic quality of life (QOL) from the ATLAS trial. Methods and results Device-specific QOL was the primary PRO using the Florida Patient Acceptance Survey (FPAS) at 1-and 6-months post-implantation. Secondary outcomes included generic QOL using the Medical Outcomes Survey (SF-36) pre-implant and 6-months post-implantation. FPAS and SF-36 were analyzed using ANCOVA. Pain measured using a Numeric Rating Scale, at 1-and 6-months, anesthetic, BMI and within/between differences were analyzed using descriptive statistics and mixed-effects linear models (MLM). Of the 503 patients randomized in ATLAS, 404 had complete FPAS data to include in this analysis. Participant characteristics were balanced. There were no significant differences between S-ICD and TV-ICD for FPAS or SF-36, across timepoints. Mean total FPAS scores increased from 73.73 (16.09) to 77.05 (16.13) and 74.43 (15.35) to 78.25 (15.88) for S-ICD and TV-ICD, respectively, (p <0.001). PROs suggested that both devices were associated with good QOL. Conclusion Device-specific and generic QOL were similar between S-ICD and TV-ICD groups up to 6-months post-implantation indicating that regardless of device type, both groups reported good device specific QOL in ATLAS patients. S-ICD patients reported higher pain scores at implant, but pain decreased by 6 months. The findings offer evidence that can be included during shared decision-making. The inclusion of patient partners in ATLAS provided opportunity to measure PROs that were deemed important to patients. Registration ClinialTrials.gov # NCT02881255
目的 患者报告结果(PROs)为了解患者对医疗设备的接受程度提供了重要依据。ATLAS 是一项随机、多中心、开放标签临床试验,最近报告称与 TV-ICD 相比,S-ICD 患者的围手术期并发症更少。本研究报告了 ATLAS 试验的 PROs,包括设备特异性和一般生活质量 (QOL)。方法和结果 设备特异性 QOL 是植入后 1 个月和 6 个月佛罗里达患者接受度调查 (FPAS) 的主要 PRO。次要结果包括植入前和植入后 6 个月使用医疗结果调查 (SF-36) 得出的一般 QOL。FPAS 和 SF-36 采用方差分析。采用描述性统计和混合效应线性模型(MLM)对1个月和6个月时的疼痛、麻醉剂、体重指数和内/间差异进行了分析。在ATLAS随机抽取的503名患者中,有404名患者拥有完整的FPAS数据,可纳入本次分析。参与者的特征是均衡的。在不同时间点,S-ICD 和 TV-ICD 在 FPAS 或 SF-36 方面没有明显差异。S-ICD 和 TV-ICD 的 FPAS 平均总分分别从 73.73 (16.09) 增加到 77.05 (16.13),74.43 (15.35) 增加到 78.25 (15.88)(pamp &;lt;0.001)。PROs表明,两种设备都具有良好的QOL。结论 S-ICD 组和 TV-ICD 组在植入后 6 个月内的设备特异性 QOL 和一般 QOL 相似,表明无论设备类型如何,两组 ATLAS 患者均报告了良好的设备特异性 QOL。S-ICD 患者在植入时的疼痛评分较高,但在 6 个月后疼痛有所减轻。研究结果为共同决策提供了证据。将患者伙伴纳入 ATLAS 为测量患者认为重要的 PROs 提供了机会。注册 ClinialTrials.gov # NCT02881255
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引用次数: 0
Incidence and assessment of delirium following open cardiac surgery; A systematic review and meta-analysis 开胸心脏手术后谵妄的发生率和评估;系统回顾和荟萃分析
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-29 DOI: 10.1093/eurjcn/zvae066
Nadja Buch Petersson, Malene Haugaard Hansen, Jacob V B Hjelmborg, Irene Instenes, Anne Sofie Christoffersen, Katrine Lawaetz Larsen, Henrik Schmidt, Lars Peter Schødt Riber, Tone Merete Norekvål, Britt Borregaard
Aim This systematic review and meta-analysis sought i) to provide an overview of the incidence of delirium following open cardiac surgery and ii) to investigate how incidences of delirium are associated with different assessment tools. Methods and results A systematic search of studies investigating delirium following open cardiac surgery were conducted in Medline (Ovid), EMBASE, PsycINFO, CiNAHL and the Cochrane Database. Only studies with patients diagnosed or screened with a validated tool were included. Studies published from 2005 to 2021 were included in the meta-analysis. Of 7,126 individual studies retrieved, 106 met the inclusion criteria for the meta-analysis, hereof 31% of high quality. The weighted pooled incidence of delirium following open cardiac surgery across all studies was 23% (95% CI 20-26%), however we found a considerable heterogeneity (I2 = 99%), which could not be explained by subgroups or further sensitivity analyses. The most commonly applied screening tool for delirium is CAM/CAM-ICU. The lowest estimates of delirium were found by applying the Delirium Observation Scale (incidence 14%, 95% CI 8-20%), and the highest estimates in studies using “other” screening tools (Organic Brain Symptom Scale, Delirium Symptom Interview) pooled incidence of 43%, (95% CI 19 - 66%), however, only two studies applied these. Conclusion Delirium following open cardiac surgery remains a complication with a high incidence of overall 23%, when applying a validated tool for screening or diagnosis. Nevertheless, this systematic review and meta-analyses highlight the significant inconsistency in current evidence regarding assessment tools and regimens. Registration Prospero CRD42020215519
目的 本系统综述和荟萃分析旨在 i) 概述开胸心脏手术后谵妄的发生率;ii) 研究谵妄的发生率与不同评估工具之间的关系。方法与结果 在 Medline (Ovid)、EMBASE、PsycINFO、CiNAHL 和 Cochrane 数据库中对开胸手术后谵妄的研究进行了系统检索。仅纳入使用有效工具诊断或筛查患者的研究。荟萃分析纳入的研究发表于 2005 年至 2021 年。在检索到的 7126 项研究中,106 项符合荟萃分析的纳入标准,其中 31% 为高质量研究。在所有研究中,开胸心脏手术后谵妄的加权汇总发生率为23%(95% CI 20-26%),但我们发现存在相当大的异质性(I2 = 99%),这无法通过亚组或进一步的敏感性分析来解释。最常用的谵妄筛查工具是CAM/CAM-ICU。使用谵妄观察量表对谵妄的估计值最低(发生率为14%,95% CI为8-20%),使用 "其他 "筛查工具(脑器质性症状量表、谵妄症状访谈)的研究对谵妄的估计值最高,汇总发生率为43%(95% CI为19-66%),但只有两项研究使用了这些工具。结论 开胸心脏手术后谵妄仍是一种并发症,在应用有效工具进行筛查或诊断时,其发生率较高,总体为 23%。尽管如此,本系统综述和荟萃分析强调了目前有关评估工具和方案的证据存在严重的不一致性。注册 Prospero CRD42020215519
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引用次数: 0
The patient experience of in-hospital telemetry monitoring: a qualitative analysis. 院内遥测监护的患者体验:定性分析。
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-12 DOI: 10.1093/eurjcn/zvad082
Marianne Sætrang Holm, Nina Fålun, Bjørn Bendz, Bengt Fridlund, Jørund Langørgen, Trond R Pettersen, Kristin E Sandau, Tone M Norekvål

Aims: In-hospital telemetry monitoring has been an integrated part of arrhythmia monitoring for decades. A substantial proportion of patients require arrhythmia monitoring during stays in non-intensive care units. However, studies exploring patients' experiences of telemetry monitoring are scarce. Therefore, the aim was to explore and describe patients' experiences of in-hospital telemetry monitoring in a non-intensive care setting.

Methods and results: Twenty face-to-face, semi-structured interviews were conducted. Interviews were conducted before discharge at two university hospitals in Norway. The patients were purposively sampled, resulting in a well-balanced population comprising 11 men and nine women, mean age 62 years (range 25-83). Average monitoring time was 9 days (range 3-14). Data were audiotaped, transcribed verbatim, and coded using NVivo software. Qualitative content analysis using an inductive approach was performed. Patients expressed a need for individualized information during telemetry monitoring. Their feelings of safety were related to responses from nurses from the central monitoring station when alarms from the telemetry were triggered. Despite perceived physical restrictions and psychological limitations associated with telemetry monitoring, they found monitoring to be beneficial because it facilitated the diagnosis of arrhythmia. Moreover, they expressed a need for improvements in wearable monitoring equipment. Patients expressed ambivalent feelings about discontinuing the telemetry and their readiness for discharge.

Conclusion: Patients need individualized information about the results of their telemetry monitoring in order to better understand the arrhythmia management and to increase their experience of safety after discharge. The limitations patients experienced should be taken into consideration in further upgrades of telemetry monitoring equipment.

目的:几十年来,院内遥测监测一直是心律失常监测的一个组成部分。相当一部分患者在非重症监护病房住院期间需要接受心律失常监测。然而,探讨患者对遥测监护体验的研究却很少。因此,本研究旨在探讨和描述非重症监护环境中患者对院内遥测监护的体验:进行了 20 次面对面的半结构化访谈。访谈在挪威两所大学医院的出院前进行。对患者进行了有目的的抽样调查,结果显示,患者的组成非常均衡,包括 11 名男性和 9 名女性,平均年龄为 62 岁(25-83 岁不等)。平均监测时间为 9 天(3-14 天不等)。数据采用 NVivo 软件进行录音、逐字记录和编码。采用归纳法进行定性内容分析。患者表示在遥测监护期间需要个性化的信息。他们的安全感与中央监护站护士在遥测警报触发时的反应有关。尽管他们认为遥测监护存在身体限制和心理限制,但他们认为监护是有益的,因为这有助于诊断心律失常。此外,他们还表示需要改进可穿戴式监测设备。患者对停止遥测和准备出院表示矛盾:结论:患者需要关于遥测监测结果的个性化信息,以便更好地了解心律失常管理,并增加出院后的安全体验。在进一步升级遥测监护设备时,应考虑到患者所经历的局限性。
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引用次数: 0
Prognostic role of sarcopenia on major adverse cardiac events among patients who underwent successful percutaneous coronary intervention: a retrospective cohort study. 成功接受经皮冠状动脉介入治疗的患者中,肌肉疏松症对主要不良心脏事件的预后作用:一项回顾性队列研究。
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-12 DOI: 10.1093/eurjcn/zvad080
Mi Hwa Won, Kyeong Ho Yun, Heeseon Kim, Youn-Jung Son

Aims: We investigated the prevalence of sarcopenia and its influence on 1-year major adverse cardiac events (MACEs) in patients after successful percutaneous coronary intervention (PCI).

Methods and results: This retrospective medical record review using purposive sampling was conducted at a tertiary care university hospital in Korea. Medical records of a total of 303 patients (≥40 years) who underwent successful PCI between January 2014 and December 2020 were analysed. We retrospectively assessed sarcopenia at initial admission. Sarcopenia was assessed by a sarcopenia index based on a ratio of serum creatinine to serum cystatin C. MACE rates were evaluated within l year after PCI. A Kaplan-Meier analysis with a log-rank test was performed to compare the time with 1-year MACE event-free survival between groups with and without sarcopenia. Cox proportional hazards regression was conducted to assess sarcopenia's influence on MACE. The prevalence of sarcopenia and 1-year MACE after PCI were 24.8 and 8.6%, respectively. We found that sarcopenia at admission (hazard ratio, 3.01; 95% confidence interval, 1.22-7.38, P = 0.017) was significantly associated with 1-year MACE among patients after PCI.

Conclusion: Expanding knowledge of sarcopenia among cardiovascular nurses may aid in early recognition of patients at risk of sarcopenia. Our finding implies that the sarcopenia index based on serum creatinine and cystatin C may be available as a prognostic factor for MACE in patients undergoing PCI. Future studies should be conducted to prospectively validate the sarcopenia index with a multi-centre, large sample.

目的:我们调查了经皮冠状动脉介入治疗(PCI)成功后患者中肌肉疏松症的患病率及其对 1 年主要心脏不良事件(MACE)的影响:这项回顾性病历审查在韩国一家三级医疗大学医院进行,采用了有目的的抽样调查。我们分析了 2014 年 1 月至 2020 年 12 月期间成功接受 PCI 治疗的 303 名患者(≥40 岁)的病历。我们回顾性地评估了最初入院时的肌肉疏松症。根据血清肌酐与血清胱抑素C的比值,用肌少症指数对肌少症进行评估。采用Kaplan-Meier分析和log-rank检验,比较有肌少症组和无肌少症组的1年无MACE事件存活时间。采用 Cox 比例危险度回归评估肌肉疏松症对 MACE 的影响。肌肉疏松症的发病率和 PCI 后 1 年 MACE 的发生率分别为 24.8% 和 8.6%。我们发现,入院时的肌肉疏松症(危险比为3.01;95%置信区间为1.22-7.38,P = 0.017)与PCI术后患者的1年MACE显著相关:扩大心血管护士对肌肉疏松症的了解有助于及早识别有肌肉疏松症风险的患者。我们的研究结果表明,基于血清肌酐和胱抑素 C 的肌肉疏松指数可作为 PCI 患者 MACE 的预后因素。未来的研究应通过多中心、大样本的前瞻性验证肌少症指数。
{"title":"Prognostic role of sarcopenia on major adverse cardiac events among patients who underwent successful percutaneous coronary intervention: a retrospective cohort study.","authors":"Mi Hwa Won, Kyeong Ho Yun, Heeseon Kim, Youn-Jung Son","doi":"10.1093/eurjcn/zvad080","DOIUrl":"10.1093/eurjcn/zvad080","url":null,"abstract":"<p><strong>Aims: </strong>We investigated the prevalence of sarcopenia and its influence on 1-year major adverse cardiac events (MACEs) in patients after successful percutaneous coronary intervention (PCI).</p><p><strong>Methods and results: </strong>This retrospective medical record review using purposive sampling was conducted at a tertiary care university hospital in Korea. Medical records of a total of 303 patients (≥40 years) who underwent successful PCI between January 2014 and December 2020 were analysed. We retrospectively assessed sarcopenia at initial admission. Sarcopenia was assessed by a sarcopenia index based on a ratio of serum creatinine to serum cystatin C. MACE rates were evaluated within l year after PCI. A Kaplan-Meier analysis with a log-rank test was performed to compare the time with 1-year MACE event-free survival between groups with and without sarcopenia. Cox proportional hazards regression was conducted to assess sarcopenia's influence on MACE. The prevalence of sarcopenia and 1-year MACE after PCI were 24.8 and 8.6%, respectively. We found that sarcopenia at admission (hazard ratio, 3.01; 95% confidence interval, 1.22-7.38, P = 0.017) was significantly associated with 1-year MACE among patients after PCI.</p><p><strong>Conclusion: </strong>Expanding knowledge of sarcopenia among cardiovascular nurses may aid in early recognition of patients at risk of sarcopenia. Our finding implies that the sarcopenia index based on serum creatinine and cystatin C may be available as a prognostic factor for MACE in patients undergoing PCI. Future studies should be conducted to prospectively validate the sarcopenia index with a multi-centre, large sample.</p>","PeriodicalId":50493,"journal":{"name":"European Journal of Cardiovascular Nursing","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10353124","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Are exercise prescriptions for patients with cardiovascular disease, made by physiotherapists, in agreement with European recommendations? 理疗师为心血管疾病患者开具的运动处方是否符合欧洲建议?
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-12 DOI: 10.1093/eurjcn/zvad065
Nastasia Marinus, Véronique Cornelissen, Raf Meesen, Karin Coninx, Dominique Hansen

Aims: Physiotherapists often treat patients with (elevated risk for) cardiovascular disease (CVD), and should thus be able to provide evidence-based exercise advice to these patients. This study, therefore, aims to examine whether exercise prescriptions by physiotherapists to patients with CVD are in accordance with European recommendations.

Methods and results: This prospective observational survey included forty-seven Belgian physiotherapists. The participants agreed to prescribe exercise intensity, frequency, session duration, program duration, and exercise type (endurance or strength training) for the same three patient cases. Exercise prescriptions were compared between physiotherapists and relations with their characteristics were studied. The agreement between physiotherapists' exercise prescriptions and those from European recommendations ('agreement score': based on a maximal score of 60/per case) was assessed. A wide inter-clinician variability was noticed for all exercise modalities, leading to a large variance for total peak-effort training minutes (from 461 up to 9000 over the three cases). The exercise frequency was prescribed fully out of range of the recommendations and the prescription of additional exercise modes was generally flawed. Exercise intensity and program duration were prescribed partially correct. The addition of strength exercises and session duration was prescribed correctly. This led to physiotherapist agreement scores of 25.3 ± 9.6, 23.2 ± 9.9, and 27.1 ± 10.6 (all out of 60), for cases one, two, and three, respectively. A greater agreement score was found in younger colleagues and those holding a Ph.D.

Conclusion: Exercise prescriptions for CVD patients vary widely among physiotherapists and often disagree with European recommendations.

Registration: ClinicalTrials.gov NCT05449652.

目的:物理治疗师经常为心血管疾病(CVD)高风险患者提供治疗,因此应该能够为这些患者提供循证运动建议。因此,本研究旨在探讨物理治疗师为心血管疾病患者开具的运动处方是否符合欧洲建议:这项前瞻性观察调查包括 47 名比利时物理治疗师。参与者同意为相同的三个病例开具运动强度、频率、疗程时间、项目持续时间和运动类型(耐力或力量训练)的处方。对物理治疗师之间的运动处方进行了比较,并研究了运动处方与物理治疗师特征之间的关系。评估了物理治疗师的运动处方与欧洲建议的运动处方之间的一致性("一致性评分":基于每例最高 60 分)。在所有运动方式中,医生之间的差异都很大,导致总峰值努力训练分钟数的差异也很大(三个病例中从 461 分钟到 9000 分钟不等)。运动频率的处方完全超出了建议范围,额外运动模式的处方普遍存在缺陷。运动强度和项目持续时间的建议部分正确。增加力量练习和疗程时间的处方是正确的。因此,物理治疗师对病例一、病例二和病例三的一致性评分分别为 25.3 ± 9.6、23.2 ± 9.9 和 27.1 ± 10.6(满分均为 60 分)。年轻同事和拥有博士学位的同事的一致得分更高:物理治疗师对心血管疾病患者的运动处方差异很大,而且往往与欧洲的建议不一致:注册:ClinicalTrials.gov NCT05449652。
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引用次数: 0
Kinesiophobia and associated variables in patients with heart failure. 心力衰竭患者的运动恐惧症及相关变量。
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-12 DOI: 10.1093/eurjcn/zvad072
Trinidad Sentandreu-Mañó, Pallav Deka, Luis Almenar, José M Tomás, Francisco-José Ferrer-Sargues, Raquel López-Vilella, Leonie Klompstra, Elena Marques-Sule

Aims: Patients with heart failure (HF) can exhibit kinesiophobia, an excessive, debilitating, and irrational fear of movement. This study aimed to enhance the understanding of kinesiophobia in patients with HF by analysing associations with the following variables: musculoskeletal pain, quality of life, quality of sleep, functional capacity, disability, frailty, sex, and age.

Methods and results: In this cross-sectional study, 107 participants were included, with ages ranging from 28 to 97 years (57% men, mean age 73.18 ± 12.68 years). Multiple regression analyses were performed with all variables, including polynomial regressions for variables with a non-linear relationship. Kinesiophobia was significantly correlated (P < 0.01) with musculoskeletal pain, quality of life, quality of sleep, functional capacity, disability, and being at risk of frailty, while age and sex were not statistically significant. Frailty disability and musculoskeletal pain intensity were variables linearly associated with kinesiophobia, while quality of sleep and disability had a non-linear relationship with kinesiophobia.

Conclusion: Kinesiophobia needs to be evaluated and better understood in patients with HF to improve physical activity and exercise adherence. This study found that musculoskeletal pain intensity, quality of sleep, disability, and frailty risk have a significant association with kinesiophobia in patients with HF. Our results suggest multi-dimensional associations of kinesiophobia in patients with HF, which require further examination and understanding.

目的:心力衰竭(HF)患者会表现出运动恐惧,这是一种对运动的过度、衰弱和非理性恐惧。本研究旨在通过分析运动恐惧与以下变量的关系,加深对心力衰竭患者运动恐惧的了解:肌肉骨骼疼痛、生活质量、睡眠质量、功能能力、残疾、虚弱、性别和年龄:在这项横断面研究中,共纳入 107 名参与者,年龄从 28 岁到 97 岁不等(57% 为男性,平均年龄为 73.18 ± 12.68 岁)。对所有变量进行了多元回归分析,包括对具有非线性关系的变量进行多项式回归。运动恐怖症与肌肉骨骼疼痛、生活质量、睡眠质量、功能能力、残疾和虚弱风险有明显相关性(P < 0.01),而年龄和性别在统计学上无明显意义。虚弱残疾和肌肉骨骼疼痛强度是与运动恐惧呈线性关系的变量,而睡眠质量和残疾则与运动恐惧呈非线性关系:结论:需要对高血压患者的运动恐惧进行评估并加深理解,以改善患者的体育锻炼和运动依从性。本研究发现,高血压患者的肌肉骨骼疼痛强度、睡眠质量、残疾和虚弱风险与运动恐惧有显著关联。我们的研究结果表明,心房颤动患者的运动恐惧与多方面因素有关,需要进一步研究和了解。
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引用次数: 0
Psychometric properties of the Japanese version of the Self-Care of Heart Failure Index version 7.2. 日文版心力衰竭自我护理指数 7.2 版的心理计量特性。
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-12 DOI: 10.1093/eurjcn/zvad069
Akiko Okada, Kanako Hayashi, Kanako Ichikura, Naoko P Kato, Rumi Wakabayashi, Noriko Nagao, Miyuki Tsuchihashi-Makaya

Aims: It is more important for patients with heart failure (HF) to objectively identify their self-care status. The Self-Care of Heart Failure Index (SCHFI) version 7.2 is a reliable and valid instrument comprising three scales: self-care maintenance, symptom perception, and self-care management. We aimed to translate the SCHFI v.7.2 into Japanese and test its validity and reliability.

Methods and results: This was a cross-sectional study. Two translators performed forward and backward translations between English and Japanese. To assess structural validity, confirmatory factor analyses were performed using the structure of the original version. To assess convergent validity, the associations between each scale and self-care self-efficacy were evaluated. To assess internal consistency, model-based internal consistency coefficients were calculated. Participants were 314 Japanese outpatients with HF (mean age: 72.8 ± 12.8 years). Regarding structural validity, all scales showed adequate model fit indices, supporting a two-factor structure with items similar to those in the original version. However, to improve the model fit indices, it was necessary to add error correlations for the self-care maintenance and symptom perception scales. Regarding convergent validity, all scales showed significant associations with self-care self-efficacy. Regarding internal consistency, the model-based internal consistency coefficients were sufficient for all scales (0.739, 0.908, and 0.783 for the self-care maintenance, symptom perception, and self-care management scales, respectively).

Conclusion: The Japanese version of the SCHFI v.7.2 had adequate validity and reliability. This instrument is useful for assessing self-care in Japanese HF patients. However, factors influencing self-care should be considered when interpreting results.

目的:对于心力衰竭(HF)患者来说,客观地确定其自我护理状况更为重要。心力衰竭自我护理指数(SCHFI)7.2 版是一个可靠有效的工具,包括三个量表:自我护理维持、症状感知和自我护理管理。我们旨在将 SCHFI 7.2 版翻译成日语,并测试其有效性和可靠性:这是一项横断面研究。两名翻译人员分别对英语和日语进行了正向和反向翻译。为了评估结构效度,使用原始版本的结构进行了确认性因子分析。为了评估收敛效度,对每个量表与自我护理自我效能感之间的关联进行了评估。为评估内部一致性,计算了基于模型的内部一致性系数。受试者为 314 名日本门诊高血压患者(平均年龄:72.8 ± 12.8 岁)。在结构效度方面,所有量表都显示出足够的模型拟合指数,支持双因素结构,其项目与原始版本相似。然而,为了提高模型拟合指数,有必要增加自我护理维持量表和症状感知量表的误差相关性。在收敛效度方面,所有量表均与自我护理自我效能感有显著关联。在内部一致性方面,所有量表的基于模型的内部一致性系数都是充分的(自我护理维持量表、症状感知量表和自我护理管理量表的内部一致性系数分别为0.739、0.908和0.783):日文版 SCHFI v.7.2 具有充分的有效性和可靠性。该工具可用于评估日本高血压患者的自我护理情况。然而,在解释结果时应考虑影响自我护理的因素。
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引用次数: 0
Implementation of patient education for patients with atrial fibrillation: nationwide cross-sectional survey and one-year follow-up. 对心房颤动患者实施患者教育:全国横断面调查和一年随访。
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-12 DOI: 10.1093/eurjcn/zvad066
Ina Qvist, Deirdre A Lane, Signe Stelling Risom, Jeroen M Hendriks, Anette Arbjerg Højen, Søren Paaske Johnsen, Lars Frost

Aims: Clinical practice guidelines recommend patient education for patients with atrial fibrillation (AF) as a part of holistic care, however, clinical guidelines lack detailed specification on the content, structure, and delivery of AF education programmes. To examine the implementation of education for patients with AF in Denmark in relation to coverage, organization, and content.

Methods and results: A cross-sectional survey was conducted from February to May 2021. The survey contained questions on the organization, delivery, and content of education for patients with AF from all 29 AF outpatient hospital sites in Denmark. The survey was conducted by email and telephone. One-year follow-up was done in May 2022 by email. Patient education was provided by healthcare professionals in 16 (55%) hospitals. Nurse workforce issues, management, non-prioritization, and lack of guidance for implementation were reasons for the absence of patient education in 13 (45%) hospitals. The structure of patient education differed in relation to group or individual teaching methods and six different education models were used. Content of the AF disease education was generally similar. At 1-year follow-up, another four hospitals reported offering patient education (69% in total).

Conclusion: Initially, almost half of the hospitals did not provide patient education, but at 1-year follow-up, 69% of hospitals delivered patient education. Patient education was heterogeneous in relation to delivery, frequency, and duration. Future research should address individualized patient education that may demonstrate superiority in relation to quality of life, less hospital admissions, and increased longevity.

目的:临床实践指南建议对心房颤动(房颤)患者进行患者教育,将其作为整体护理的一部分,然而,临床指南对房颤教育计划的内容、结构和实施缺乏详细规定。研究丹麦心房颤动患者教育在覆盖范围、组织和内容方面的实施情况:2021 年 2 月至 5 月期间进行了一项横向调查。调查内容包括丹麦所有 29 家心房颤动门诊医院的心房颤动患者教育的组织、实施和内容。调查通过电子邮件和电话进行。2022 年 5 月,通过电子邮件进行了为期一年的随访。16家医院(55%)的患者教育由医护人员提供。13家(45%)医院未开展患者教育的原因包括护士人力问题、管理问题、未将患者教育作为优先事项以及缺乏实施指导。患者教育的结构因集体或个人教学方法而异,共采用了六种不同的教育模式。房颤疾病教育的内容大体相似。在为期一年的随访中,另有四家医院表示提供了患者教育(共占 69%):结论:最初,几乎一半的医院没有提供患者教育,但在一年的随访中,69%的医院提供了患者教育。患者教育在提供方式、频率和持续时间方面存在差异。未来的研究应针对个体化的患者教育进行探讨,这可能会在提高生活质量、减少入院次数和延长寿命等方面显示出优越性。
{"title":"Implementation of patient education for patients with atrial fibrillation: nationwide cross-sectional survey and one-year follow-up.","authors":"Ina Qvist, Deirdre A Lane, Signe Stelling Risom, Jeroen M Hendriks, Anette Arbjerg Højen, Søren Paaske Johnsen, Lars Frost","doi":"10.1093/eurjcn/zvad066","DOIUrl":"10.1093/eurjcn/zvad066","url":null,"abstract":"<p><strong>Aims: </strong>Clinical practice guidelines recommend patient education for patients with atrial fibrillation (AF) as a part of holistic care, however, clinical guidelines lack detailed specification on the content, structure, and delivery of AF education programmes. To examine the implementation of education for patients with AF in Denmark in relation to coverage, organization, and content.</p><p><strong>Methods and results: </strong>A cross-sectional survey was conducted from February to May 2021. The survey contained questions on the organization, delivery, and content of education for patients with AF from all 29 AF outpatient hospital sites in Denmark. The survey was conducted by email and telephone. One-year follow-up was done in May 2022 by email. Patient education was provided by healthcare professionals in 16 (55%) hospitals. Nurse workforce issues, management, non-prioritization, and lack of guidance for implementation were reasons for the absence of patient education in 13 (45%) hospitals. The structure of patient education differed in relation to group or individual teaching methods and six different education models were used. Content of the AF disease education was generally similar. At 1-year follow-up, another four hospitals reported offering patient education (69% in total).</p><p><strong>Conclusion: </strong>Initially, almost half of the hospitals did not provide patient education, but at 1-year follow-up, 69% of hospitals delivered patient education. Patient education was heterogeneous in relation to delivery, frequency, and duration. Future research should address individualized patient education that may demonstrate superiority in relation to quality of life, less hospital admissions, and increased longevity.</p>","PeriodicalId":50493,"journal":{"name":"European Journal of Cardiovascular Nursing","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9870881","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Early mobilization after transcatheter aortic valve implantation: observational cohort study. 经导管主动脉瓣植入术后的早期动员:观察性队列研究。
IF 2.9 3区 医学 Q1 Nursing Pub Date : 2024-04-12 DOI: 10.1093/eurjcn/zvad081
Sandra B Lauck, Maggie Yu, Carrie Bancroft, Britt Borregaard, Jopie Polderman, Anna L Stephenson, Eric Durand, Mariama Akodad, David Meier, Holly Andrews, Leslie Achtem, Erin Tang, David A Wood, Janarthanan Sathananthan, John G Webb

Aims: Early mobilization is associated with improved outcomes in hospitalized older patients. We sought to determine the effect of a nurse-led protocol on mobilization 4 h after transfemoral transcatheter aortic valve implantation (TAVI) across different units of care.

Methods and results: We conducted a prospective observational cohort single-centre study of consecutive patients. We implemented a standardized protocol for safe early recovery and progressive mobilization in the critical care and cardiac telemetry units. We measured the time to first mobilization and conducted descriptive statistics to identify patient and system barriers to timely ambulation. We recruited 139 patients (82.5 years, SD = 6.7; 46% women). At baseline, patients who were mobilized early (≤4 h) and late (>4 h) did not differ, except for higher rates of diabetes (25.5% vs. 43.9%, P = 0.032) and peripheral arterial disease (8.2% vs. 26.8%, P = 0.003) in the late mobilization group. The median time to mobilization was 4 h [inter-quartile range (IQR) 3.25, 4]; 98 patients (70.5%) were mobilized successfully after 4 h of bedrest; 118 (84.9%) were walking by the evening of the procedure (<8 h bedrest); and 21 (15.1%) were on bedrest overnight and mobilized the following day. Primary reasons for overnight bedrest were arrhythmia monitoring (n = 10, 7.2%) and haemodynamic and/or neurological instability (n = 6, 4.3%); six patients (4.3%) experienced delayed ambulation due to system issues. Procedure location in the hybrid operating room and transfer to critical care were associated with longer bedrest times.

Conclusion: Standardized nurse-led mobilization 4 h after TF TAVI is feasible in the absence of clinical complications and system barriers.

目的:早期动员与改善住院老年患者的预后有关。我们试图确定在不同的护理单元中,由护士主导的方案对经食道经导管主动脉瓣植入术(TAVI)术后 4 小时动员的影响:我们对连续患者进行了前瞻性单中心队列观察研究。我们在重症监护室和心脏遥测室实施了安全早期恢复和逐步移动的标准化方案。我们测量了首次移动的时间,并进行了描述性统计,以确定患者和系统在及时移动方面的障碍。我们招募了 139 名患者(82.5 岁,SD = 6.7;46% 为女性)。基线时,早期动员(≤4 小时)和晚期动员(>4 小时)的患者没有差异,只是晚期动员组的糖尿病(25.5% 对 43.9%,P = 0.032)和外周动脉疾病(8.2% 对 26.8%,P = 0.003)发病率更高。动员时间的中位数为4小时[四分位数间距(IQR)为3.25,4];98名患者(70.5%)在卧床4小时后成功动员;118名患者(84.9%)在术后当晚就能行走(结论:在没有临床并发症和系统障碍的情况下,TF TAVI术后4小时在护士指导下进行标准化移动是可行的。
{"title":"Early mobilization after transcatheter aortic valve implantation: observational cohort study.","authors":"Sandra B Lauck, Maggie Yu, Carrie Bancroft, Britt Borregaard, Jopie Polderman, Anna L Stephenson, Eric Durand, Mariama Akodad, David Meier, Holly Andrews, Leslie Achtem, Erin Tang, David A Wood, Janarthanan Sathananthan, John G Webb","doi":"10.1093/eurjcn/zvad081","DOIUrl":"10.1093/eurjcn/zvad081","url":null,"abstract":"<p><strong>Aims: </strong>Early mobilization is associated with improved outcomes in hospitalized older patients. We sought to determine the effect of a nurse-led protocol on mobilization 4 h after transfemoral transcatheter aortic valve implantation (TAVI) across different units of care.</p><p><strong>Methods and results: </strong>We conducted a prospective observational cohort single-centre study of consecutive patients. We implemented a standardized protocol for safe early recovery and progressive mobilization in the critical care and cardiac telemetry units. We measured the time to first mobilization and conducted descriptive statistics to identify patient and system barriers to timely ambulation. We recruited 139 patients (82.5 years, SD = 6.7; 46% women). At baseline, patients who were mobilized early (≤4 h) and late (>4 h) did not differ, except for higher rates of diabetes (25.5% vs. 43.9%, P = 0.032) and peripheral arterial disease (8.2% vs. 26.8%, P = 0.003) in the late mobilization group. The median time to mobilization was 4 h [inter-quartile range (IQR) 3.25, 4]; 98 patients (70.5%) were mobilized successfully after 4 h of bedrest; 118 (84.9%) were walking by the evening of the procedure (<8 h bedrest); and 21 (15.1%) were on bedrest overnight and mobilized the following day. Primary reasons for overnight bedrest were arrhythmia monitoring (n = 10, 7.2%) and haemodynamic and/or neurological instability (n = 6, 4.3%); six patients (4.3%) experienced delayed ambulation due to system issues. Procedure location in the hybrid operating room and transfer to critical care were associated with longer bedrest times.</p><p><strong>Conclusion: </strong>Standardized nurse-led mobilization 4 h after TF TAVI is feasible in the absence of clinical complications and system barriers.</p>","PeriodicalId":50493,"journal":{"name":"European Journal of Cardiovascular Nursing","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10049263","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
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European Journal of Cardiovascular Nursing
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