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异构性先天性心脏病患者伴有呼吸纤毛功能障碍时,术后呼吸并发症增加。

Increased postoperative respiratory complications in heterotaxy congenital heart disease patients with respiratory ciliary dysfunction.

机构信息

Children's National Heart Institute, Children's National Medical Center, Washington, DC.

Office of Biostatistics Research, National Institutes of Health, Bethesda, Md.

出版信息

J Thorac Cardiovasc Surg. 2014 Apr;147(4):1291-1298.e2. doi: 10.1016/j.jtcvs.2013.06.018. Epub 2013 Jul 22.

Abstract

OBJECTIVE(S): Congenital heart disease (CHD) and heterotaxy patients have increased postoperative and respiratory complications. We recently showed CHD-heterotaxy patients can have respiratory ciliary dysfunction (CD) similar to that associated with primary ciliary dyskinesia, including low nasal nitric oxide and abnormal ciliary motion. In this study, we investigated whether CHD-heterotaxy patients with CD may have worse postsurgical outcomes.

METHODS

We examined postsurgical outcome in 13 heterotaxy-CHD patients with CD (25 surgeries), compared with 14 heterotaxy-CHD patients without CD (27 surgeries). Outcome data were collected for each surgery, including respiratory complications, tracheostomy, use of inhaled β-agonists or nitric oxide, length of hospital stay, days on ventilator, and death.

RESULTS

The CD versus the no-CD CHD cohorts had similar Risk Adjustment in Congenital Heart Surgery-1 risk categories, repair track, age at surgery, and follow-up evaluation times. Respiratory complications (76% vs 37%; P = .006), need for tracheostomy (16% vs 0%; P = .047), and use of inhaled β-agonists (64% vs 11%; P = .0001) all were increased significantly in heterotaxy-CHD patients with CD. No significant differences were detected in postoperative hospital stay, days on mechanical ventilation, or surgical mortality. A trend toward increased mortality for the CD group beyond the postoperative period was observed (33% vs 0%; P = .055) in patients younger than age 10 years.

CONCLUSIONS

Our findings showed that heterotaxy-CHD patients with CD may have increased risks for respiratory deficiencies. Overall, there was a trend toward increased mortality in CD patients with intermediate follow-up evaluation. Because β-agonists are known to increase ciliary beat frequency, presurgical screening for CD and perioperative treatment of CD patients with inhaled β-agonists may improve postoperative outcomes and survival.

摘要

目的

先天性心脏病(CHD)和内脏转位患者术后和呼吸系统并发症增加。我们最近发现,CHD-内脏转位患者可能存在与原发性纤毛运动障碍相关的呼吸纤毛功能障碍(CD),包括鼻一氧化氮降低和纤毛运动异常。在这项研究中,我们研究了 CD 的 CHD-内脏转位患者是否可能有更差的术后结果。

方法

我们检查了 13 例 CD 的内脏转位-CHD 患者(25 例手术)和 14 例无 CD 的内脏转位-CHD 患者(27 例手术)的术后结果。收集了每例手术的结果数据,包括呼吸系统并发症、气管切开术、使用吸入β-激动剂或一氧化氮、住院时间、呼吸机使用天数和死亡。

结果

CD 与无 CD 的 CHD 组在风险调整心脏手术 1 风险类别、修复途径、手术年龄和随访评估时间方面相似。CD 组的呼吸系统并发症(76%对 37%;P=.006)、需要气管切开术(16%对 0%;P=.047)和使用吸入β-激动剂(64%对 11%;P=.0001)的发生率均显著增加。CD 组的术后住院时间、呼吸机使用天数或手术死亡率无显著差异。在年龄小于 10 岁的患者中,观察到 CD 组的死亡率在术后有增加的趋势(33%对 0%;P=.055)。

结论

我们的发现表明,CD 的内脏转位-CHD 患者可能存在呼吸缺陷的风险增加。总的来说,在有中间随访评估的 CD 患者中,死亡率有增加的趋势。由于β-激动剂已知可增加纤毛的拍打频率,因此在术前筛查 CD 并在围手术期为 CD 患者使用吸入β-激动剂可能会改善术后结果和生存率。

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