Mendel Brian, Kohar Kelvin, Yumnanisha Defin Allevia, Djiu Richie Jonathan, Winarta Justin, Prakoso Radityo, Siagian Sisca Natalia
Division of Pediatric Cardiology and Congenital Heart Disease, Department of Cardiology and Vascular Medicine, National Cardiovascular Center Harapan Kita, Universitas Indonesia, Jakarta, Indonesia.
Department of Cardiology and Vascular Medicine, Sultan Sulaiman Government Hospital, Serdang Bedagai, North Sumatera, Indonesia.
Int J Cardiol Congenit Heart Dis. 2023 Nov 18;15:100485. doi: 10.1016/j.ijcchd.2023.100485. eCollection 2024 Mar.
Untreated critical pulmonary stenosis may develop into pulmonary atresia with intact ventricular septum, which is associated with a high risk of morbidity and mortality both in fetuses and neonates. In this meta-analysis, we sought to discover the potential of fetal pulmonary valvuloplasty that might affect patients' survival compared to other available procedures.
This systematic review and meta-analysis were conducted based on the PRISMA guideline. The authors thoroughly searched the recognized and potential interventions for PA-IVS, including FPV, total ventricular repair, and palliative procedures. The primary outcome was the mortality rate. We used R software (version 4.1.3) to calculate the overall proportion using the random-effects model of proportional meta-analysis.
The FPV procedure was performed at a mean gestational age of 26.28 weeks (95%CI: 24.83-27.73) and was successful in 87.6 % (95 % CI: 78.3-96.3 %) of patients. A total of 52.9 % patients attained biventricular circulation postnatally (95 % CI: 31.2-74.7 %). Successful FPV was associated with a slightly higher overall mortality rate [periprocedural death 4.7 % (95%CI: 0-10.7 %) and postnatal death 8 % (95%CI: 3-13 %)] compared to the three currently available definitive therapies, namely the Fontan procedure [10 % (95%CI: 4-17 %)], 1.5V repair [11 % (95%CI: 5-17 %), and 2V repair [8 % (95%CI: 1-15 %)].
FPV can potentially increase the likelihood of biventricular circulation in fetuses with critical pulmonary valve stenosis.
未经治疗的严重肺动脉狭窄可能发展为室间隔完整的肺动脉闭锁,这在胎儿和新生儿中均与高发病率和死亡率相关。在这项荟萃分析中,我们试图探究与其他可用手术相比,胎儿肺动脉瓣成形术对患者生存的潜在影响。
本系统评价和荟萃分析依据PRISMA指南进行。作者全面检索了已认可的和潜在的针对室间隔完整的肺动脉闭锁(PA-IVS)的干预措施,包括胎儿肺动脉瓣成形术(FPV)、全心室修复和姑息性手术。主要结局为死亡率。我们使用R软件(版本4.1.3)通过比例荟萃分析的随机效应模型计算总体比例。
FPV手术的平均孕周为26.28周(95%置信区间:24.83 - 27.73),87.6%(95%置信区间:78.3 - 96.3%)的患者手术成功。共有52.9%的患者出生后实现双心室循环(95%置信区间:31.2 - 74.7%)。与目前可用的三种确定性治疗方法相比,即Fontan手术[10%(95%置信区间:4 - 17%)]、1.5V修复[11%(95%置信区间:5 - 17%)]和2V修复[8%(95%置信区间:1 - 15%)],成功的FPV手术总体死亡率略高[围手术期死亡4.7%(95%置信区间:0 - 10.7%),出生后死亡8%(95%置信区间:3 - 13%)]。
FPV可能会增加患有严重肺动脉瓣狭窄胎儿实现双心室循环的可能性。