Sánchez-Becerra Janneth Cristina, Guillén-Torres Rogelio, Becerra-Becerra Rosario, Márquez-González Horacio, Ibarra-Ríos Daniel
Neonatology Department, National Institute of Health, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Cardiology Department, National Institute of Health, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Front Pediatr. 2023 Mar 23;11:1104940. doi: 10.3389/fped.2023.1104940. eCollection 2023.
Increased recognition of the development of chronic pulmonary hypertension (cPH) in preterm infants with chronic lung disease (CLD) has prompted enhanced monitoring for the identification of different phenotypes.
All newborns consulted for oxygen/respiratory support dependency (CLD assessment) from January 2018 to December 2021 were included. TnECHO and LUS screening for cPH-CLD were performed at 36 weeks postmenstrual age. Cases of cPH related to increased pulmonary blood flow (cPH-IPBF) were referred to Pediatric Cardiology. The objective of the study was to identify all cases of cPH (cPH-CLD/IPBF) in the CLD patients screened and to compare outcomes. Following a standardized algorithm, cPH-CLD patients were treated with diuretics; ultrasounds taken before and after treatment were analyzed.
Seventy-two patients with CLD were screened. Twenty-two (30%) had cPH-CLD, and nine (12%) had cPH-IPBF. cPH infants underwent more days of mechanical ventilation, were more likely to have retinopathy of prematurity, and showed increased mortality. The LUS pattern observed in the 72 CLD patients consisted of a thickened pleural line and a B-line interstitial heterogeneous pattern; 29% of patients were found to have lung consolidations. After diuretic therapy, step-down in respiratory support occurred in 59% of neonates with cPH-CLD. A decrease in respiratory rate (RR), right ventricular output (RVO), markers of pulmonary vascular resistance (PVR), and B-line pattern was observed. In tissue Doppler imaging, biventricular diastolic function was found to be modified after diuretics.
CLD infants with cPH showed increased morbidity and mortality. In cPH-CLD patients, a decrease in RR and step-down in respiratory support was observed after diuretic treatment. Follow-up ultrasound showed a decrease in RVO, markers of PVR, and B-lines.
对患有慢性肺病(CLD)的早产儿慢性肺动脉高压(cPH)发展的认识不断提高,促使加强监测以识别不同表型。
纳入2018年1月至2021年12月期间因依赖氧气/呼吸支持(CLD评估)而就诊的所有新生儿。在孕龄36周时进行经胸超声心动图(TnECHO)和肺部超声(LUS)筛查cPH-CLD。与肺血流量增加相关的cPH(cPH-IPBF)病例转诊至儿科心脏病科。本研究的目的是识别筛查的CLD患者中的所有cPH病例(cPH-CLD/IPBF)并比较结局。按照标准化算法,cPH-CLD患者接受利尿剂治疗;分析治疗前后的超声检查结果。
筛查了72例CLD患者。22例(30%)患有cPH-CLD,9例(12%)患有cPH-IPBF。cPH婴儿接受机械通气的天数更多,更易患早产儿视网膜病变,且死亡率更高。在72例CLD患者中观察到的LUS模式包括胸膜线增厚和B线间质异质性模式;29%的患者有肺实变。利尿剂治疗后,59%的cPH-CLD新生儿呼吸支持降级。观察到呼吸频率(RR)、右心室输出量(RVO)、肺血管阻力(PVR)标志物和B线模式降低。在组织多普勒成像中,发现利尿剂治疗后双心室舒张功能发生改变。
患有cPH的CLD婴儿发病率和死亡率增加。在cPH-CLD患者中,利尿剂治疗后观察到RR降低和呼吸支持降级。随访超声显示RVO、PVR标志物和B线减少。