Lindberg L, Olsson A K, Jögi P, Jonmarker C
Division of Heart and Lung, Section of Pediatric Cardiac Surgery, University Hospital, Lund, Sweden.
J Thorac Cardiovasc Surg. 2002 Jun;123(6):1155-63. doi: 10.1067/mtc.2002.121497.
Pulmonary hypertension may result in significant morbidity and mortality after pediatric cardiac surgery. The objective of this study was to determine the incidence and outcome of severe pulmonary hypertension, defined as a ratio of pulmonary to systemic arterial pressure equal to or greater than 1.0, after cardiac surgery in children.
Data from all children younger than 18 years who had undergone cardiothoracic surgery from January 1, 1994, to December 31, 1998, were examined. To find children with severe pulmonary hypertension, we reviewed intensive care unit charts from patients who had been monitored with a pulmonary artery catheter after the operation (n = 151), had received mechanical ventilation for more than 4 days after the operation (n = 124), or had died in the operating room or the intensive care unit (n = 22). Intraoperative and postoperative measurements of mean pulmonary arterial pressure and postoperative echocardiographic studies during the first 3 postoperative days were used to select the children.
During the study period, 1349 children (including 164 neonates and 511 infants, median age 12 months) underwent cardiac operations with an overall perioperative mortality of 22 patients (1.6%). Twenty-seven children (2%, median age 4.2 months) had severe pulmonary hypertension. Of these, 2 (7.4%) died within 30 days of the operation, and 3 others (11%) died within a year (median follow-up 53 months). Nitric oxide inhalation was used in 5 of the 27 cases, and it probably saved the life of 1 patient, may have helped in 1 case, and had no discernible effect in 3 cases. Severe pulmonary hypertension was most common after correction of complete atrioventricular septal defects (14%, n = 12/85). Thirteen of 131 children with Down syndrome (9.9%) had severe pulmonary hypertension.
Severe postoperative pulmonary hypertension occurred after 2% of the cardiac procedures and in most cases was managed successfully with conventional treatment and had a favorable postoperative outcome. The low incidence relative to previous reports may reflect the benefits of early correction and improved intraoperative and postoperative care.
肺动脉高压可能导致小儿心脏手术后出现显著的发病率和死亡率。本研究的目的是确定儿童心脏手术后严重肺动脉高压(定义为肺动脉与体动脉压力之比等于或大于1.0)的发生率及转归。
检查了1994年1月1日至1998年12月31日期间所有接受心胸外科手术的18岁以下儿童的数据。为找出患有严重肺动脉高压的儿童,我们查阅了术后接受肺动脉导管监测的患者(n = 151)、术后接受机械通气超过4天的患者(n = 124)或在手术室或重症监护病房死亡的患者(n = 22)的重症监护病房病历。术中及术后平均肺动脉压的测量以及术后头3天内的超声心动图检查用于筛选儿童。
在研究期间,1349名儿童(包括164名新生儿和511名婴儿,中位年龄12个月)接受了心脏手术,围手术期总死亡率为22例患者(1.6%)。27名儿童(2%,中位年龄4.2个月)患有严重肺动脉高压。其中,2例(7.4%)在术后30天内死亡,另外3例(11%)在1年内死亡(中位随访53个月)。27例中有5例使用了一氧化氮吸入,可能挽救了1例患者的生命,对1例可能有帮助,对3例无明显效果。严重肺动脉高压在完全房室间隔缺损矫正术后最为常见(14%,n = 12/85)。131名唐氏综合征儿童中有13名(9.9%)患有严重肺动脉高压。
严重的术后肺动脉高压发生在2%的心脏手术之后,大多数情况下通过传统治疗成功处理,术后转归良好。相对于先前报告而言较低的发生率可能反映了早期矫正以及术中及术后护理改善的益处。