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

被引:52
作者
Harden, Brandon [1 ]
Tian, Xin [3 ]
Giese, Rachel [4 ]
Nakhleh, Nader [2 ]
Kureshi, Safina [2 ]
Francis, Richard [6 ]
Hanumanthaiah, Sridhar [1 ]
Li, You [6 ]
Swisher, Matthew [4 ]
Kuehl, Karen [1 ]
Sami, Iman [2 ]
Olivier, Kenneth [5 ]
Jonas, Richard [1 ]
Lo, Cecilia W. [6 ]
Leatherbury, Linda [1 ]
机构
[1] Childrens Natl Med Ctr, Childrens Natl Heart Inst, Washington, DC 20010 USA
[2] Childrens Natl Med Ctr, Dept Pediat Pulmonol, Washington, DC 20010 USA
[3] NIH, Off Biostat Res, Bethesda, MD 20892 USA
[4] NIH, Howard Hughes Med Inst, Bethesda, MD 20892 USA
[5] NIAID, NIH, Bethesda, MD 20892 USA
[6] Univ Pittsburgh, Sch Med, Dept Dev Biol, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
PEDIATRIC CARDIAC-SURGERY; BEAT FREQUENCY; PREVALENCE; DYSKINESIA; DEFECTS; MANAGEMENT; ISOMERISM;
D O I
10.1016/j.jtcvs.2013.06.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 beta-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 beta-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 b-agonists are known to increase ciliary beat frequency, presurgical screening for CD and perioperative treatment of CD patients with inhaled beta-agonists may improve postoperative outcomes and survival.
引用
收藏
页码:1291 / U287
页数:10
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