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一项针对针灸与假针刺对照研究的方案设计,纳入了患有内科疾病的急性住院老年患者,旨在评估该治疗方案对谵妄的疗效。该研究为随机对照临床试验,将患者分为单纯标准治疗组、假针刺组和针灸组。

The study protocol for a randomized, controlled trial of acupuncture versus a sham procedure versus standard care alone for the treatment of delirium in acutely hospitalized older adults with a medical illness.

机构信息

Internal Medicine B Department, Bnai Zion Medical Center, Haifa, Israel.

Complementary Medicine Department, Bnai Zion Medical Center, Haifa, Israel; School of Public Health, University of Haifa, Haifa, Israel.

出版信息

Maturitas. 2019 Jun;124:72-80. doi: 10.1016/j.maturitas.2019.03.001. Epub 2019 Mar 7.

DOI:10.1016/j.maturitas.2019.03.001
PMID:31097183
Abstract

BACKGROUND

Many hospitalized older adults experience delirium, but treatment options are limited. Acupuncture has been shown to improve cognitive function and reduce agitation in dementia. We hypothesize that acupuncture, when compared with a sham intervention, will reduce the duration and severity of delirium, normalize delirium biomarkers, and improve clinical outcomes related to delirium in acutely hospitalized older adults with a medical illness.

METHODS

This three-arm, prospective, randomized, clinical trial will evaluate adults aged over 65 years who are acutely hospitalized to an internal-medicine ward and diagnosed with delirium or subsyndromal delirium. The 288 patients (96 in each of three groups) will be randomly allocated to receive either daily true acupuncture with usual care, a daily sham procedure with usual care, or usual care only in a 1:1:1 distribution for up to one week or until the patient is delirium-free for over 48 h. Other delirium and clinical interventions will remain unchanged. Delirium will be diagnosed using DSM-5 criteria and its severity will be assessed using the long Confusion Assessment Method Severity (CAM-S) tool.

OUTCOMES

The primary study outcome will be the daily CAM-S score over 7 days between the three groups. Secondary outcomes will include time to first resolution of the delirium (over 7 days), the proportion of days spent delirium-free, daily antipsychotic use, daily pain scores, sleep quality, morning serum cortisol and T3 levels, and midnight urinary cortisol/creatinine ratio, all determined twice a week, and delirium-related complications. Hospital mortality, duration of hospital stay and functional status at discharge will also be compared between the three groups. Adverse events potentially related to acupuncture will be evaluated daily. The cost-effectiveness of acupuncture will be estimated.

CONCLUSION

This novel randomized study will evaluate both the specific and the non-specific effects of acupuncture on delirium, and related outcomes, and its safety. Potential mechanism(s) of action for acupuncture in reducing delirium will be explored and healthcare-related costs estimated. Positive study results may prove pivotal in facilitating a multimodal, non-pharmacologic, integrative approach to delirium treatment among older, medical inpatients.

摘要

背景

许多住院的老年患者会出现谵妄,但治疗选择有限。针刺已被证明可改善痴呆患者的认知功能和减少激越。我们假设与假针刺干预相比,针刺治疗可缩短谵妄的持续时间和严重程度,使谵妄生物标志物正常化,并改善与急性住院内科老年患者谵妄相关的临床结局。

方法

这是一项三臂、前瞻性、随机、临床试验,将评估年龄在 65 岁以上、因内科疾病急性住院并被诊断为谵妄或亚综合征性谵妄的成年人。288 例患者(每组 96 例)将被随机分配接受每日真针刺联合常规护理、每日假针刺联合常规护理或仅接受常规护理,为期 1 周或直至患者谵妄持续时间超过 48 小时且无谵妄。其他谵妄和临床干预措施保持不变。采用 DSM-5 标准诊断谵妄,并使用长版意识模糊评估法(CAM-S)工具评估其严重程度。

结局

主要研究结局为三组患者 7 天内每日 CAM-S 评分。次要结局包括:首次缓解谵妄的时间(7 天内)、无谵妄天数比例、每日抗精神病药使用、每日疼痛评分、睡眠质量、清晨血清皮质醇和 T3 水平、午夜尿皮质醇/肌酐比值(每周两次测定),以及谵妄相关并发症。还将比较三组患者的住院死亡率、住院时间和出院时的功能状态。每日评估与针刺相关的潜在不良事件。估计针刺的成本效益。

结论

这项新的随机研究将评估针刺对谵妄及其相关结局的特异性和非特异性作用及其安全性。探索针刺降低谵妄的潜在作用机制,并估计医疗相关成本。阳性研究结果可能对促进针对老年内科住院患者的多模式、非药物、综合性谵妄治疗方法具有重要意义。

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