Caruthers Regine L, Kempa Mollie, Loo Angela, Gulbransen Erin, Kelly Elizabeth, Erickson Steven R, Hirsch Jennifer C, Schumacher Kurt R, Stringer Kathleen A
Department of Pharmacy, University of Michigan Hospitals and Health Centers, Ann Arbor, MI, USA.
Pediatr Cardiol. 2013 Feb;34(2):256-61. doi: 10.1007/s00246-012-0430-5. Epub 2012 Jul 15.
Plastic bronchitis (PB) is a poorly understood disease that can complicate any underlying pulmonary disease. However, it appears to most often occur in patients with surgically palliated congenital heart disease, particularly after the Fontan procedure. Few data exist about the prevalence and etiology of PB in this population. In an effort to establish data about prevalence, we conducted a retrospective study of an existing Fontan surgery database (n = 654) comprised of data, including sex, age at date of surgery, alive/dead status, New York Heart Association classification at last follow-up, right-ventricular end-diastolic pressure and pulmonary artery pressure before Fontan surgery, and the presence of a Fontan fenestration. An initial medical record review of 173 patients in the database who were followed at the University of Michigan identified seven patients with PB resulting in an estimated prevalence of 4 %. Subsequently, 14 % of 211 surveyed patients reported that they presently expectorate mucus or fibrin plugs (casts). Demographic and clinical variables did not differ between patients with or without possible PB. Collectively, these findings suggest that Fontan patients presently with PB may range from 4 to 14 %, indicating potential under-diagnosis of the disease. There were no remarkable physical or hemodynamic indicators that differentiated patients with or without possible PB. These data also highlight the need for more elaborate, prospective studies to improve our understanding of PB pathogenesis so that more definitive diagnostic criteria for this devastating disease can be established and its prevalence more accurately determined.
塑性支气管炎(PB)是一种了解甚少的疾病,可使任何潜在的肺部疾病复杂化。然而,它似乎最常发生在接受姑息性手术的先天性心脏病患者中,尤其是在Fontan手术之后。关于该人群中PB的患病率和病因的数据很少。为了确定患病率数据,我们对一个现有的Fontan手术数据库(n = 654)进行了回顾性研究,该数据库包含的数据有性别、手术时年龄、存活/死亡状态、最后一次随访时的纽约心脏协会分级、Fontan手术前的右心室舒张末期压力和肺动脉压力,以及是否存在Fontan开窗。对密歇根大学随访的数据库中的173名患者进行的初步病历审查发现7例PB患者,估计患病率为4%。随后,在接受调查的211名患者中,14%报告他们目前咳出黏液或纤维蛋白栓(铸型)。有或没有可能患PB的患者在人口统计学和临床变量方面没有差异。总体而言,这些发现表明,目前Fontan手术患者中患PB的比例可能在4%至14%之间,这表明该疾病可能存在诊断不足的情况。没有明显的体格检查或血流动力学指标能区分有或没有可能患PB的患者。这些数据还凸显了开展更详尽的前瞻性研究的必要性,以增进我们对PB发病机制的理解,从而能够建立针对这种严重疾病更明确的诊断标准,并更准确地确定其患病率。