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采用肺动脉环缩术创建主肺动脉窗对左心发育不全综合征并非良好的姑息治疗方法。

Creation of aorto-pulmonary window with pulmonary artery band is not good palliation for hypoplastic left heart syndrome.

作者信息

Hosein Riad B M, Mehta Chetan, Stickley John, Mcguirk Simon P, Jones Timothy J, Brawn William J, Barron David J

机构信息

Department of Cardiac Surgery, Birmingham Children's Hospital, United Kingdom.

出版信息

Eur J Cardiothorac Surg. 2007 Nov;32(5):745-50. doi: 10.1016/j.ejcts.2007.07.024. Epub 2007 Sep 14.

Abstract

OBJECTIVE

A small sub-group of patients with hypoplastic left heart syndrome (HLHS) have normal-sized ascending aorta and arch. An alternative to the Norwood I procedure in these patients is the creation of an aorto-pulmonary (AP) window with a distal pulmonary artery band (PAB). We reviewed our experience with this technique and compared outcomes to the Norwood procedure for HLHS.

METHODS

All patients treated for HLHS in a single institution between 1992 and 2005 were analysed. This identified 13 patients treated with AP window and PAB compared to 333 patients undergoing stage I Norwood procedure. An unrestrictive AP window was created and the main PA was banded. Patient records and echocardiograms were analysed. Median follow-up was 10 (IQR 0-655) days and 100% complete.

RESULTS

There were seven early deaths (54%) in the AP window group and two conversions to Norwood circulation. This was a significantly worse outcome than for the Norwood procedure over the same period, which had an early mortality of 29% (p=0.03). Kaplan-Meier actuarial analysis demonstrated a continued survival benefit of the Norwood group at 6 months (p=0.0005). Deaths were due to either low cardiac output syndrome (n=4) or sudden unheralded arrest (n=3). This occurred despite aortic cross-clamp and circulatory arrest times being significantly lower in the AP window group compared to the Norwood group (35+/-27 vs 55+/-16 min, p<0.01 and 16+/-29 vs 55+/-20 min, p<0.01, respectively). No differences in arterial saturations or systolic blood pressure existed between the groups, but diastolic blood pressure was significantly lower in the AP window group at 27+/-10 mmHg compared to 42+/-8 mmHg in the Norwood group (p=0.01) with evidence of flow reversal in the descending aorta. Differences in diastolic blood pressure between groups were abolished after conversion to stage II.

CONCLUSIONS

Despite favourable anatomy and shorter ischaemic times, the AP window/PAB technique has a poor outcome compared to the Norwood procedure for HLHS. Low diastolic blood pressure with reversal of descending aortic flow in diastole was a feature of the AP window/PAB circulation. We recommend the Norwood procedure for these sub-types. This may have implications for newer 'hybrid' procedures for HLHS which create a similar palliative circulation.

摘要

目的

一小部分左心发育不全综合征(HLHS)患者的升主动脉和主动脉弓大小正常。对于这些患者,诺伍德I型手术的替代方法是创建一个带远端肺动脉环扎术(PAB)的主-肺动脉(AP)窗。我们回顾了我们使用该技术的经验,并将结果与HLHS的诺伍德手术进行了比较。

方法

分析了1992年至2005年在单一机构接受HLHS治疗的所有患者。这确定了13例接受AP窗和PAB治疗的患者,与之相比,有333例患者接受了I期诺伍德手术。创建了一个无限制的AP窗,并对主肺动脉进行环扎。分析了患者记录和超声心动图。中位随访时间为10(四分位间距0 - 655)天,且随访完整率为100%。

结果

AP窗组有7例早期死亡(54%),2例转为诺伍德循环。这一结果明显比同期诺伍德手术更差,同期诺伍德手术的早期死亡率为29%(p = 0.03)。Kaplan - Meier生存分析显示,诺伍德组在6个月时持续存在生存优势(p = 0.0005)。死亡原因要么是低心排血量综合征(n = 4),要么是突然意外骤停(n = 3)。尽管AP窗组的主动脉交叉阻断和循环阻断时间明显低于诺伍德组(分别为35±27分钟对55±16分钟,p < 0.01;16±29分钟对55±20分钟,p < 0.01),但仍出现了上述情况。两组之间动脉血氧饱和度或收缩压无差异,但AP窗组的舒张压明显更低,为27±10 mmHg,而诺伍德组为42±8 mmHg(p = 0.01),且降主动脉有血流逆转的证据。转为II期手术后,两组之间的舒张压差异消失。

结论

尽管解剖结构有利且缺血时间较短,但与HLHS的诺伍德手术相比,AP窗/PAB技术的结果较差。舒张期降主动脉血流逆转导致的低舒张压是AP窗/PAB循环的一个特征。我们建议对这些亚型采用诺伍德手术。这可能对创建类似姑息性循环的HLHS新“杂交”手术有影响。

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