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Effect of prophylactic non-invasive mechanical ventilation on functional capacity after heart valve replacement: a clinical trial

机译:预防性非侵入性机械通气对心脏瓣膜置换术后功能能力的影响:一项临床试验

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ABSTRACT OBJECTIVE: During cardiac surgery, several factors contribute to the development of postoperative pulmonary complications. Non-invasive ventilation is a promising therapeutic tool for improving the functionality of this type of patient. The aim of this study is to evaluate the functional capacity and length of stay of patients in a nosocomial intensive care unit who underwent prophylactic non-invasive ventilation after heart valve replacement. METHOD: The study was a controlled clinical trial, comprising 50 individuals of both sexes who were allocated by randomization into two groups with 25 patients in each group: the control group and experimental group. After surgery, the patients were transferred to the intensive care unit and then participated in standard physical therapy, which was provided to the experimental group after 3 applications of non-invasive ventilation within the first 26 hours after extubation. For non-invasive ventilation, the positive pressure was 10 cm H 2 O, with a duration of 1 hour. The evaluation was performed on the 7 th postoperative day/discharge and included a 6-minute walk test. The intensive care unit and hospitalization times were monitored in both groups. Brazilian Registry of Clinical Trials (REBeC): RBR number 8bxdd3. RESULTS: Analysis of the 6-minute walk test showed that the control group walked an average distance of 264.34???±76 meters and the experimental group walked an average distance of 334.07???±71 meters ( p =0.002). The intensive care unit and hospitalization times did not differ between the groups. CONCLUSION: Non-invasive ventilation as a therapeutic resource was effective toward improving functionality; however, non-invasive ventilation did not influence the intensive care unit or hospitalization times of the studied cardiac patients.
机译:摘要目的:在心脏外科手术中,多种因素会导致术后肺部并发症的发生。无创通气是改善此类患者功能的有前途的治疗工具。这项研究的目的是评估在医院内重症监护病房中更换心脏瓣膜后进行预防性无创通气的患者的功能能力和住院时间。方法:该研究是一项对照临床试验,包括50位男女,随机分为两组,每组25名患者:对照组和实验组。手术后,将患者转移到重症监护室,然后参加标准的物理治疗,在拔管后的头26小时内进行3次无创通气后,将其提供给实验组。对于无创通气,正压为10 cm H 2 O,持续时间为1小时。评估是在术后第7天/出院时进行的,包括6分钟的步行测试。两组均监测重症监护病房和住院时间。巴西临床试验注册中心(REBeC):RBR号8bxdd3。结果:对6分钟步行测试的分析表明,对照组的平均步行距离为264.34×±76米,实验组的平均步行距离为334.07×±71米(p = 0.002)。重症监护病房和住院时间在两组之间没有差异。结论:无创通气作为一种治疗资源可有效改善功能。但是,无创通气不会影响所研究的心脏病患者的重症监护病房或住院时间。

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    《Clinics》 |2017年第10期|共页
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  • 中图分类 临床医学;
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