Soongswang J, Adatia I, Newman C, Smallhorn J F, Williams W G, Freedom R M
Division of Cardiology, The Hospital for Sick Children and University of Toronto, Ontario, Canada.
J Am Coll Cardiol. 1998 Sep;32(3):753-7. doi: 10.1016/s0735-1097(98)00310-6.
We reviewed the factors contributing to or causing death before surgery in neonates with d-transposition of the great arteries (TGA) despite anatomy suitable for the arterial switch operation (ASO) to develop strategies to minimize preoperative attrition.
Currently the ASO for neonates with TGA carries a low operative mortality. However, there is a paucity of information regarding the patients who die before the ASO. Strategies to ensure survival to operation are of importance to improve overall outcome.
We reviewed all neonates with TGA and patent forearm ovale (PFO) < or = 2 mm, a birthweight <2 kg, or who died before surgery, between 1988 and 1996.
We identified 12 out of 295 neonates with TGA (4.1%) with anatomy suitable for the ASO who died prior to surgery. All had TGA/intact ventricular septum (IVS) and presented with a severely restrictive PFO. In 11 of 12 cases the cause of death was attributed to the sequelae of profound hypoxemia from inadequate mixing. Contributing factors were prematurity, 41.7%; severe respiratory distress syndrome, 25%; and persistent pulmonary hypertension of the newborn (PPHN), 16.7%. All patients received prostaglandin E1 (PGE1) infusion. Urgent balloon atrial sepstostomy (BAS) was performed in 66.7% with improved oxygenation. No cases were diagnosed prenatally. In contrast, all patients with a PFO < or = 2 mm who survived to ASO had a significantly better response to PGE1 infusion (p=0.03) than nonsurvivors. The ASO was accomplished without mortality in four of nine with a weight <2 kg.
Of those neonates admitted with TGA, 4.1% died before surgery. Eleven of 12 (3.7%) died due to consequences of inadequate interatrial mixing despite PGE1 infusion. Earlier diagnosis and BAS are critically important in determining survival. Early ASO may improve survival in patients weighing <2 kg. Prenatal diagnosis with delivery in a high-risk obstetrical unit with facilities for immediate BAS and supportive therapy for pulmonary hypertension and ventricular failure may be necessary to salvage this group of patients.
我们回顾了尽管大动脉d型转位(TGA)新生儿的解剖结构适合动脉调转术(ASO),但在手术前导致死亡的因素,以制定策略尽量减少术前损耗。
目前,TGA新生儿的ASO手术死亡率较低。然而,关于在ASO手术前死亡患者的信息却很少。确保存活至手术的策略对于改善总体预后至关重要。
我们回顾了1988年至1996年间所有患有TGA且动脉导管未闭(PFO)≤2mm、出生体重<2kg或在手术前死亡的新生儿。
我们在295例患有TGA且解剖结构适合ASO的新生儿中确定了12例(4.1%)在手术前死亡。所有患儿均为TGA/室间隔完整(IVS),且伴有严重限制性PFO。12例中有11例死亡原因是由于混合不足导致严重低氧血症的后遗症。促成因素包括早产,占41.7%;严重呼吸窘迫综合征,占25%;以及新生儿持续性肺动脉高压(PPHN),占16.7%。所有患者均接受前列腺素E1(PGE1)输注。66.7%的患者接受了紧急球囊房间隔造口术(BAS),氧合情况有所改善。所有病例均未在产前确诊。相比之下,所有存活至ASO手术的PFO≤2mm患者对PGE1输注的反应明显优于未存活者(p=0.03)。9例体重<2kg的患者中有4例成功完成ASO手术且无死亡。
在那些因TGA入院的新生儿中,4.1%在手术前死亡。12例中有11例(3.7%)尽管接受了PGE1输注,但因心房混合不足的后果而死亡。早期诊断和BAS对于确定存活率至关重要。早期ASO可能会提高体重<2kg患者的存活率。对于这组患者,可能需要在具备立即进行BAS以及对肺动脉高压和心力衰竭进行支持治疗设施的高危产科病房进行产前诊断并分娩,以挽救他们的生命。