Wang Chen-Hong, Shi Li-Ping, Ma Xiao-Lu, DU Li-Zhong
Department of Neonatal Intensive Care Unit, Children's Hospital, Zhejiang University School of Medicine, Hangzhou 310052, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2018 Nov;20(11):893-896. doi: 10.7499/j.issn.1008-8830.2018.11.003.
To study the clinical features and prognosis of bronchopulmonary dysplasia (BPD) complicated by pulmonary hypertension (PH) in preterm infants.
A retrospective analysis was performed on the clinical data of 191 preterm infants with BPD.
In the 191 preterm infants with BPD, 37 (19.4%), all with moderate or severe BPD, developed PH beyond 36 weeks' corrected age. The incidence rates of PH in infants with moderate and severe BPD were 5.7% (5/87) and 47.8% (32/67) respectively. Gestational age and birth weight were lower in infants with PH than in those without PH (P<0.01). Infants with PH had higher incidence rates of small for gestational age (SGA), severe BPD, surgical ligation of patent ductus arteriosus (PDA), neonatal respiratory distress syndrome, hemodynamically significant PDA, and pneumonia than those without PH (P<0.01). Durations of oxygen therapy, intubation, and positive pressure ventilation were longer in infants with PH than in those without PH (P<0.01). Infants with PH had higher incidence rates of retinopathy of prematurity and extrauterine growth retardation, a higher mortality, and a longer length of hospital stay compared with those without PH (P<0.01). In the 37 infants with PH (6 with mild PH, 14 with moderate PH, and 17 with severe PH), those with mild or moderate PH all survived; 15(88%) out of 17 infants with severe PH died.
The incidence of PH is high in preterm infants with moderate or severe BPD. Regular screening of pulmonary artery pressure is recommended for infants with BPD. Infants with low gestational age and birth weight, SGA, and severe BPD are more likely to develop PH. Infants with BPD complicated by PH have relatively high incidence rates of complications, high mortality, and poor prognosis.
研究早产儿支气管肺发育不良(BPD)合并肺动脉高压(PH)的临床特征及预后。
对191例BPD早产儿的临床资料进行回顾性分析。
191例BPD早产儿中,37例(19.4%)在矫正年龄36周后出现PH,均为中重度BPD。中重度BPD患儿的PH发生率分别为5.7%(5/87)和47.8%(32/67)。发生PH的患儿胎龄和出生体重低于未发生PH的患儿(P<0.01)。与未发生PH的患儿相比,发生PH的患儿小于胎龄儿(SGA)、重度BPD、动脉导管未闭(PDA)手术结扎、新生儿呼吸窘迫综合征、血流动力学显著的PDA及肺炎的发生率更高(P<0.01)。发生PH的患儿氧疗、插管及正压通气时间长于未发生PH的患儿(P<0.01)。与未发生PH的患儿相比,发生PH的患儿早产儿视网膜病变和宫外生长发育迟缓的发生率更高,死亡率更高,住院时间更长(P<0.01)。在37例发生PH的患儿中(轻度PH 6例,中度PH 14例,重度PH 17例),轻度或中度PH患儿均存活;17例重度PH患儿中15例(88%)死亡。
中重度BPD早产儿PH发生率高。建议对BPD患儿定期筛查肺动脉压力。胎龄和出生体重低、SGA及重度BPD患儿更易发生PH。BPD合并PH患儿并发症发生率相对较高,死亡率高,预后差。