Levin D L, Heymann M A, Kitterman J A, Gregory G A, Phibbs R H, Rudolph A M
J Pediatr. 1976 Oct;89(4):626-30. doi: 10.1016/s0022-3476(76)80405-2.
Persistent pulmonary hypertension of the newborn infant can be difficult to distinguish from other cardiopulmonary causes of cyanosis during the newborn period. Infants with PPHN have cyanosis, tachypnea, acidemia, normal pulmonary parenchymal markings on the chest radiography, and anatomically normal hearts. We have identified and treated 11 infants and have noted several signs and symptoms not previously emphasized. These are cineangiocardiographic evidence of atrioventricular valve insufficiency in association with systolic murmurs and slow ventricular emptying, apnea, hypocalcemia, only a small rise in abdominal aortic blood oxygen tension during breathing of 100% oxygen, and no response to continuous positive airway pressure. Right-to-left shunting through the patent ductus arteriosus was documented in nine infants: in all six of those in whom simultaneous temporal and abdominal aortic blood oxygen tension measurements were made; in three by means of cardiac catheterization. Ten infants survived after variable courses and treatments which makes it difficult to ascribe improvement to any one therapy. The distinct increase in blood oxygen tension with tolazoline HCl and curare in some instances is discussed.
新生儿持续性肺动脉高压在新生儿期可能难以与其他导致发绀的心肺病因相区分。患有PPHN的婴儿会出现发绀、呼吸急促、酸血症,胸部X线片上肺实质纹理正常,心脏解剖结构正常。我们已确诊并治疗了11名婴儿,并注意到一些此前未被重点强调的体征和症状。这些包括:与收缩期杂音及心室排空缓慢相关的房室瓣关闭不全的心血管造影证据、呼吸暂停、低钙血症、在吸入100%氧气时腹主动脉血氧张力仅小幅升高,以及对持续气道正压通气无反应。9名婴儿记录到经动脉导管未闭的右向左分流:在所有6名同时进行颞部和腹主动脉血氧张力测量的婴儿中;在3名通过心导管检查的婴儿中。10名婴儿经过不同病程和治疗后存活,这使得难以将病情改善归因于任何一种治疗方法。文中讨论了在某些情况下盐酸妥拉唑啉和箭毒使血氧张力明显升高的情况。