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先天性肺动脉瓣环发育不良的严重程度与法洛四联症的远期预后:回顾性队列研究。

Severity of native pulmonary annular hypoplasia and late outcomes of tetralogy of Fallot: retrospective cohort study.

机构信息

Pediatric Heart Centre, Children's Research Centre, University Children's Hospital, Zurich, Switzerland.

Epidemiology, Biostatistics and Prevention Institute, Department of Biostatistics, University of Zurich, Zurich, Switzerland.

出版信息

Swiss Med Wkly. 2024 Nov 1;154:3689. doi: 10.57187/s.3689.

DOI:10.57187/s.3689
PMID:39509552
Abstract

OBJECTIVE

Pulmonary annular hypoplasia and valvar dysplasia are key morphological features affecting long-term outcomes of tetralogy of Fallot. This retrospective study aimed to analyse factors affecting contemporary long-term outcomes with a focus on pulmonary annular growth and function over time.

METHODS

131 consecutive isolated tetralogy of Fallot repairs performed between 2004 and 2014 at University Children's Hospital Zurich were included. Median age and weight at the time of repair were 4.8 (interquartile range [IQR] 3.2-6.3) months and 6.1 (IQR 5.1-7) kg, respectively. Based on the severity of native pulmonary annular hypoplasia, the cohort was divided into group 1 (preoperative pulmonary annular Z score < -4; n = 20), group 2 (Z score -2 to -4; n = 56) and group 3 (Z score > -2; n = 54). A transannular patch was used in 88/131 (67.2%) patients: 80%, 67.9% and 61.1% in groups 1, 2 and 3, respectively. The primary outcome was defined as right ventricular outflow tract (RVOT) reoperation or pulmonary valve replacement. Secondary outcome was composite pulmonary valve dysfunction defined as peak gradient >40 mm Hg or severe pulmonary regurgitation at follow-up. A multiple Cox regression model was used to quantify the association of age at tetralogy of Fallot repair, preoperative pulmonary annular Z score and RVOT approach with primary and secondary outcome. Follow-up was 98.5% complete, with a median follow-up duration of 9.6 (95% confidence interval [CI] 9-10.4) years.

RESULTS

All patients were alive at last follow-up resulting in 100% survival. 20/131 patients underwent pulmonary valve replacement (14 surgical and 6 catheter interventional) while 5/131 underwent RVOT reoperations other than valve replacement. The Kaplan-Meier 10-year freedom from primary outcome was 85% (95% CI 78-92%); 69% (46-100%), 91% (82-100%) and 84% (74-95%) for groups 1, 2 and 3, respectively (log rank p = 0.16). Composite dysfunction at follow-up was observed in 29.8% (overall): 45%, 28.6% and 25.9% for groups 1, 2 and 3, respectively (p = 0.12). The multiple Cox regression analysis for primary outcome indicated that the use of a transannular patch results in a Hazard Ratio (HR) of 3.3 (95% CI 0.7-14.7, p = 0.13). Additionally, the presence of composite dysfunction at discharge results in a HR of 2.1 (95% CI 0.8-5.4, p = 0.1). Age (in months) with a HR of 0.8 (95% CI 0.6-1, p = 0.06) and group 2 with a HR of 0.4 (95% CI 0.14-1.2, p = 0.11) showed a trend to being protective for the primary outcome. However, the 95% CI of all estimates included the HR of 1.

CONCLUSIONS

Transannular patch use and composite dysfunction at discharge, although not statistically significant at 5% level, may be associated with pulmonary valve replacement and RVOT reoperation. Avoiding the use of a transannular patch or using reconstructive techniques to achieve a better composite dysfunction at discharge could reduce the primary outcome. Large multicentre studies are needed to demonstrate more precisely the impact of pulmonary annulus Z scores on outcome.

摘要

目的

肺动脉瓣环发育不良和瓣叶发育不良是影响法洛四联症长期预后的关键形态学特征。本回顾性研究旨在分析影响当代长期预后的因素,重点关注肺动脉瓣环的生长和功能随时间的变化。

方法

纳入了 2004 年至 2014 年在苏黎世大学儿童医院接受的 131 例连续的法洛四联症修复手术。修复时的中位年龄和体重分别为 4.8(四分位距 [IQR] 3.2-6.3)个月和 6.1(IQR 5.1-7)kg。根据肺动脉瓣环发育不良的严重程度,将队列分为 3 组:第 1 组(术前肺动脉瓣环 Z 评分<-4;n=20)、第 2 组(Z 评分-2 至-4;n=56)和第 3 组(Z 评分>-2;n=54)。131 例患者中有 88 例(67.2%)使用了跨瓣环补片:第 1、2 和 3 组中分别有 80%、67.9%和 61.1%的患者使用了该补片。主要结局定义为右心室流出道(RVOT)再次手术或肺动脉瓣置换。次要结局定义为随访时峰值梯度>40mmHg 或严重肺动脉瓣反流的复合肺动脉瓣功能障碍。使用多 Cox 回归模型来量化法洛四联症修复时的年龄、术前肺动脉瓣环 Z 评分和 RVOT 方法与主要和次要结局的相关性。随访率为 98.5%,中位随访时间为 9.6(95%置信区间 [CI] 9-10.4)年。

结果

所有患者在最后一次随访时均存活,总生存率为 100%。20/131 例患者接受了肺动脉瓣置换(14 例手术和 6 例导管介入),5/131 例患者接受了除瓣膜置换以外的 RVOT 再次手术。Kaplan-Meier 10 年无主要结局的生存率为 85%(95%CI 78-92%);第 1、2 和 3 组分别为 69%(46-100%)、91%(82-100%)和 84%(74-95%)(对数秩检验 p=0.16)。随访时发现 29.8%(总体)存在复合功能障碍:第 1、2 和 3 组分别为 45%、28.6%和 25.9%(p=0.12)。多 Cox 回归分析主要结局表明,使用跨瓣环补片的 HR 为 3.3(95%CI 0.7-14.7,p=0.13)。此外,出院时存在复合功能障碍的 HR 为 2.1(95%CI 0.8-5.4,p=0.1)。年龄(以月为单位)的 HR 为 0.8(95%CI 0.6-1,p=0.06)和第 2 组的 HR 为 0.4(95%CI 0.14-1.2,p=0.11)显示出对主要结局的保护趋势。然而,所有估计的 95%CI 都包含了 HR 为 1 的情况。

结论

尽管在 5%水平上没有统计学意义,但跨瓣环补片的使用和出院时的复合功能障碍可能与肺动脉瓣置换和 RVOT 再次手术相关。避免使用跨瓣环补片或使用重建技术来改善出院时的复合功能障碍可能会降低主要结局的发生率。需要进行大型多中心研究来更精确地显示肺动脉瓣环 Z 评分对结局的影响。

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