The impact of closed suction wound drainage on chronic pain and health-related quality of life after posterior spinal fusion in patients with adolescent idiopathic scoliosis.

IF 4.9 1区 医学 Q1 ORTHOPEDICS
Linda Helenius, Paul Gerdhem, Matti Ahonen, Johanna Syvänen, Jenni Jalkanen, Yrjänä Nietosvaara, Ilkka Helenius
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引用次数: 0

Abstract

Aims: Closed suction subfascial drainage is widely used after instrumented posterior spinal fusion in patients with a spinal deformity. The aim of this study was to determine the effect of this wound drainage on the outcomes in patients with adolescent idiopathic scoliosis (AIS). This was a further analysis of a randomized, multicentre clinical trial reporting on patients after posterior spinal fusion using segmental pedicle screw instrumentation. In this study the incidence of deep surgical site infection (SSI) and chronic postoperative pain at two years' follow-up are reported.

Methods: We conducted a randomized, multicentre clinical trial on adolescents undergoing posterior spinal fusion for AIS using segmental pedicle screw instrumentation. A total of 90 consecutive patients were randomized into a 'drain' or 'no drain' group at the time of wound closure, using the sealed envelope technique (1:1). The primary outcomes in the initial study were the change in the level of haemoglobin in the blood postoperatively and total blood loss. A secondary outcome was the opioid consumption immediately after surgery. The aim of this further study was to report the rate of deep SSI and persistent postoperative pain, at two years' follow-up.

Results: As previously reported, the mean 48-hour opioid consumption was significantly higher in the no drain group (2.0 mg/kg (SD 0.8) vs 1.4 mg/kg (SD 0.7); p = 0.005). There were no delayed deep SSIs. At two years' follow-up, the mean Scoliosis Research Society 24-item questionnaire (SRS-24) total score did not differ between the groups (4.11 (SD 0.47) vs 4.16 (SD 0.33); p = 0.910). The mean SRS-24 pain score was 4.28 (SD 0.48) in the no drain group compared with 4.33 (SD 0.66) in the drain group (p = 0.245). Seven patients (19%) in the no drain group and six in the drain group (14%) reported moderate to severe pain (numerical rating scale ≥ 4) at two years' follow-up (p = 0.484). The general self-image domain score was significantly higher in the no drain group compared with the drain group (4.02 (SD 0.74) vs 4.59 (SD 0.54); p < 0.001).

Conclusion: The main finding in this study was that more severe pain immediately after surgery did not result in a higher incidence of chronic pain in the no drain group compared with the drain group. Back pain and health-related quality of life at two years' follow-up did not differ between the groups. The patient-reported self-image domain was significantly better in the no drain group compared with the drain group.

闭合抽吸伤口引流对青少年特发性脊柱侧凸后路融合术后慢性疼痛和健康相关生活质量的影响。
目的:闭合抽吸筋膜下引流术广泛应用于脊柱畸形患者的器械后路脊柱融合术后。本研究旨在确定这种伤口引流对青少年特发性脊柱侧弯症(AIS)患者治疗效果的影响。这是对一项随机多中心临床试验的进一步分析,该试验报告了使用节段式椎弓根螺钉器械进行脊柱后路融合术的患者情况。本研究报告了深部手术部位感染(SSI)的发生率和两年随访期间的术后慢性疼痛情况:方法:我们对使用节段式椎弓根螺钉器械进行后路脊柱融合术治疗 AIS 的青少年进行了一项随机、多中心临床试验。共有 90 名连续的患者在伤口闭合时被随机分为 "引流管 "组和 "无引流管 "组,采用密封信封技术(1:1)。初步研究的主要结果是术后血液中血红蛋白水平的变化和总失血量。次要结果是术后阿片类药物的消耗量。这项进一步研究的目的是报告两年随访期间深部 SSI 和术后持续疼痛的发生率:与之前的报告一样,无引流管组的48小时阿片类药物平均用量明显更高(2.0 mg/kg (SD 0.8) vs 1.4 mg/kg (SD 0.7); p = 0.005)。无延迟性深部 SSI。在两年的随访中,脊柱侧凸研究协会 24 项调查问卷(SRS-24)的平均总分在两组之间没有差异(4.11(标清 0.47) vs 4.16(标清 0.33);p = 0.910)。无引流管组的平均 SRS-24 疼痛评分为 4.28(标清 0.48),而引流管组为 4.33(标清 0.66)(P = 0.245)。在两年的随访中,无引流管组有七名患者(19%)报告中度至重度疼痛(数字评分量表≥ 4),引流管组有六名患者(14%)报告中度至重度疼痛(p = 0.484)。与引流管组相比,无引流管组的一般自我形象领域得分明显更高(4.02 (SD 0.74) vs 4.59 (SD 0.54);P < 0.001):本研究的主要发现是,与引流管组相比,术后即刻出现更严重的疼痛并不会导致无引流管组出现更高的慢性疼痛发生率。在两年的随访中,两组患者的背痛和与健康相关的生活质量没有差异。与引流管组相比,无引流管组患者报告的自我形象域明显更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bone & Joint Journal
Bone & Joint Journal ORTHOPEDICS-SURGERY
CiteScore
9.40
自引率
10.90%
发文量
318
期刊介绍: We welcome original articles from any part of the world. The papers are assessed by members of the Editorial Board and our international panel of expert reviewers, then either accepted for publication or rejected by the Editor. We receive over 2000 submissions each year and accept about 250 for publication, many after revisions recommended by the reviewers, editors or statistical advisers. A decision usually takes between six and eight weeks. Each paper is assessed by two reviewers with a special interest in the subject covered by the paper, and also by members of the editorial team. Controversial papers will be discussed at a full meeting of the Editorial Board. Publication is between four and six months after acceptance.
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