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先天性膈疝患者术后肺血管生长。

Postoperative pulmonary vascular growth in patients with congenital diaphragmatic hernia.

机构信息

Department of Pediatric Surgery, Faculty of Medicine, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo, 113-8655, Japan.

出版信息

Pediatr Surg Int. 2024 May 7;40(1):125. doi: 10.1007/s00383-024-05706-z.

DOI:10.1007/s00383-024-05706-z
PMID:38714568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11076324/
Abstract

BACKGROUND

Postoperative pulmonary growth in congenital diaphragmatic hernias (CDH) remains unclear. We investigated postoperative pulmonary vascular growth using serial lung perfusion scintigraphy in patients with CDH.

METHODS

Neonates with left CDH who underwent surgery and postoperative lung perfusion scintigraphy at our institution between 2001 and 2020 were included. Patient demographics, clinical courses, and lung scintigraphy data were retrospectively analyzed by reviewing medical records.

RESULTS

Twenty-one patients with CDH were included. Of these, 10 underwent serial lung scintigraphy. The ipsilateral perfusion rate and median age on the 1st and serial lung scintigraphy were 32% (34 days) and 33% (3.6 years), respectively. Gestational age at prenatal diagnosis (p = 0.02), alveolar-arterial oxygen difference (A-aDO) at birth (p = 0.007), and preoperative nitric oxide (NO) use (p = 0.014) significantly correlated with the 1st lung scintigraphy. No other variables, including operative approach, were significantly correlated with the 1st or serial scintigraphy findings. All patients improved lung perfusion with serial studies [Difference:  + 7.0 (4.3-13.25) %, p = 0.001, paired t-test]. This improvement was not significantly correlated with preoperative A-aDO (p = 0.96), NO use (p = 0.28), or liver up (p = 0.90). The difference was significantly larger in patients who underwent thoracoscopic repair than in those who underwent open abdominal repair [+ 10.6 (5.0-17.1) % vs. + 4.25 (1.2-7.9) %, p = 0.042].

CONCLUSION

Our study indicated a postoperative improvement in ipsilateral lung vascular growth, which is possibly enhanced by a minimally invasive approach, in patients with CDH.

摘要

背景

先天性膈疝(CDH)患者术后肺生长情况仍不清楚。我们通过对 CDH 患者进行系列肺灌注闪烁显像来研究术后肺血管生长情况。

方法

纳入 2001 年至 2020 年期间在我院行手术治疗和术后肺灌注闪烁显像的左侧 CDH 新生儿。回顾病历,分析患者的人口统计学资料、临床病程和肺闪烁显像资料。

结果

共纳入 21 例 CDH 患者,其中 10 例行系列肺闪烁显像。患侧灌注率和第 1 次及系列肺闪烁显像的中位年龄分别为 32%(34 天)和 33%(3.6 岁)。产前诊断时的胎龄(p=0.02)、出生时的肺泡-动脉氧差(A-aDO)(p=0.007)和术前一氧化氮(NO)使用(p=0.014)与第 1 次肺闪烁显像显著相关。其他变量,包括手术方式,与第 1 次或系列闪烁显像结果均无显著相关性。所有患者的肺灌注均随系列研究而改善(差异:+7.0(4.3-13.25)%,p=0.001,配对 t 检验)。这种改善与术前 A-aDO(p=0.96)、NO 使用(p=0.28)或肝脏上移(p=0.90)均无显著相关性。胸腔镜修补术患者的差异明显大于开腹修补术患者(+10.6(5.0-17.1)% vs. +4.25(1.2-7.9)%,p=0.042)。

结论

本研究表明,CDH 患者术后患侧肺血管生长改善,微创方法可能增强这种改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbf/11076324/02717e3babd6/383_2024_5706_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbf/11076324/155411320c12/383_2024_5706_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbf/11076324/02717e3babd6/383_2024_5706_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbf/11076324/155411320c12/383_2024_5706_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbf/11076324/02717e3babd6/383_2024_5706_Fig2_HTML.jpg

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本文引用的文献

1
Longitudinal Analysis of Pulmonary Function in Survivors of Congenital Diaphragmatic Hernia.先天性膈疝幸存者的肺功能纵向分析。
J Pediatr. 2020 Jan;216:158-164.e2. doi: 10.1016/j.jpeds.2019.09.072. Epub 2019 Nov 6.
2
Longitudinal Analysis of Ventilation Perfusion Mismatch in Congenital Diaphragmatic Hernia Survivors.先天性膈疝幸存者通气灌注不匹配的纵向分析。
J Pediatr. 2020 Apr;219:160-166.e2. doi: 10.1016/j.jpeds.2019.09.053. Epub 2019 Nov 5.
3
Histogram based analysis of lung perfusion of children after congenital diaphragmatic hernia repair.
基于直方图的先天性膈疝修补术后儿童肺灌注分析。
Magn Reson Imaging. 2018 May;48:42-49. doi: 10.1016/j.mri.2017.11.013. Epub 2017 Nov 23.
4
Standardized reporting for congenital diaphragmatic hernia--an international consensus.先天性膈疝的标准化报告——国际共识。
J Pediatr Surg. 2013 Dec;48(12):2408-15. doi: 10.1016/j.jpedsurg.2013.08.014.
5
Long-term follow-up of children with congenital diaphragmatic hernia--observations from a single institution.先天性膈疝患儿的长期随访——来自单一机构的观察结果
Eur J Pediatr Surg. 2014 Dec;24(6):500-7. doi: 10.1055/s-0033-1357751. Epub 2013 Oct 25.
6
Morbidity and long-term follow-up in CDH patients.先天性膈疝患者的发病率及长期随访
Eur J Pediatr Surg. 2012 Oct;22(5):384-92. doi: 10.1055/s-0032-1329412. Epub 2012 Oct 31.
7
Postoperative regional distribution of pulmonary ventilation and perfusion in infants with congenital diaphragmatic hernia.先天性膈疝婴儿术后肺通气和灌注的区域性分布。
J Pediatr Surg. 2011 Nov;46(11):2047-53. doi: 10.1016/j.jpedsurg.2011.06.042.
8
Serial perfusion study depicts pulmonary vascular growth in the survivors of non-extracorporeal membrane oxygenation-treated congenital diaphragmatic hernia.序贯灌注研究描绘了未接受体外膜氧合治疗的先天性膈疝幸存者的肺血管生长。
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9
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Ultrasound Obstet Gynecol. 2010 May;35(5):578-82. doi: 10.1002/uog.7592.
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Mid- and long-term effects on pulmonary perfusion, anatomy and diaphragmatic motility in survivors of congenital diaphragmatic hernia.先天性膈疝幸存者肺灌注、解剖结构及膈肌运动的中长期影响
Pediatr Surg Int. 2005 Dec;21(12):954-9. doi: 10.1007/s00383-005-1557-8. Epub 2005 Oct 21.