Department of Surgery, L 223, Oregon Health & Science University, 3181 Sam Jackson Park Rd, Portland, OR 97239, USA.
J Thorac Cardiovasc Surg. 2010 Jan;139(1):119-26; discussion 126-7. doi: 10.1016/j.jtcvs.2009.04.061. Epub 2009 Nov 11.
We aimed to describe management strategies for neonates with hypoplastic left heart syndrome over the past 18 years in the United States and to identify determinants of institutional management decisions.
Neonates with hypoplastic left heart syndrome were retrospectively identified by use of the Nationwide Inpatient Sample 1988-2005. Treatment was categorized as (1) transplantation, (2) Norwood operation (as defined by Risk Adjustment in Congenital Heart Surgery), (3) transfer to another facility, or (4) no surgical intervention (comfort care).
A total of 3286 neonates were identified, yielding a national estimate of 16,781 + or - 586 cases. Of these, 2% (348 + or - 47) underwent transplantation, 16% (2767 + or - 286) had Norwood operations, 25% (4143 + or - 156) were transferred to another facility, and 57% (9523 + or - 436) had comfort care. Changes in practice patterns occurred over time, with an increasing number of neonates undergoing Norwood, concomitant with decreasing numbers undergoing transplantation (P < .001). Bias toward the Norwood operation over time paralleled a significant, nearly linear decrease in the in-hospital mortality rate for the Norwood operation, from 86% in the earliest sextile to 24% in the most recent sextile (P < .001). Prevalence of transfer to definitive care hospitals remained constant over time, as did the number of infants (approximately half) who received no surgery (comfort care).
Despite improved surgical outcomes, the majority of infants continue to receive no surgical care. There has been an increase in the number of infants offered the Norwood operation for hypoplastic left heart syndrome over the past 2 decades, which seems to have come mostly owing to a decrease of transplants. The advent of prenatal diagnosis has not decreased the proportion of neonates born at institutions unequipped to provide definitive care.
我们旨在描述过去 18 年美国患有左心发育不全综合征新生儿的管理策略,并确定机构管理决策的决定因素。
通过使用 1988 年至 2005 年的全国住院患者样本,回顾性确定患有左心发育不全综合征的新生儿。治疗分为(1)移植,(2)Norwood 手术(根据先天性心脏病手术风险调整定义),(3)转移到另一家医院,或(4)无手术干预(舒适护理)。
共确定了 3286 名新生儿,估计全国有 16781 +或-586 例。其中,2%(348 +或-47)接受了移植,16%(2767 +或-286)接受了 Norwood 手术,25%(4143 +或-156)转移到另一家医院,57%(9523 +或-436)接受了舒适护理。随着时间的推移,实践模式发生了变化,接受 Norwood 手术的新生儿数量不断增加,同时接受移植的新生儿数量不断减少(P <.001)。随着时间的推移,Norwood 手术的比例偏向于 Norwood 手术,同时 Norwood 手术的住院死亡率显著下降,从最早的六分位数的 86%下降到最近的六分位数的 24%(P <.001)。到确定性治疗医院的转移率保持不变,接受无手术(舒适护理)的婴儿数量也保持不变(约一半)。
尽管手术结果有所改善,但大多数婴儿仍未接受手术治疗。在过去的 20 年中,接受左心发育不全综合征 Norwood 手术的婴儿数量有所增加,这似乎主要是由于移植手术的减少。产前诊断的出现并没有降低在没有提供确定性治疗能力的机构出生的新生儿比例。