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羊水过少所致肺发育不全的极低出生体重儿的一氧化氮吸入治疗

Nitric oxide inhalation therapy in very low-birthweight infants with hypoplastic lung due to oligohydramnios.

作者信息

Uga Naoki, Ishii Tetsuya, Kawase Yasuhiro, Arai Hiroko, Tada Hiroshi

机构信息

Division of Neonatology, Perinatal Center, Toho University School of Medicine, Tokyo, Japan.

出版信息

Pediatr Int. 2004 Feb;46(1):10-4. doi: 10.1111/j.1442-200X.2004.01844.x.

Abstract

BACKGROUND

Although nitric oxide inhalation (iNO) therapy improves arterial oxygenation and reduces the rate of extracorporeal membrane oxygenation in term neonates, the efficacy of this therapy in premature infants is controversial. The objective of the present study was to determine whether iNO therapy improves the survival of very low-birthweight infants with pulmonary hypoplasia due to prolonged rupture of membrane.

METHODS

A retrospective comparative study of very low-birthweight infants with pulmonary hypoplasia due to oligohydramnios who had or had not been treated with iNO therapy, was performed (iNO-treated group, eight infants; control group, 10 infants). A neonate was considered to have pulmonary hypoplasia due to oligohydramnios if the following conditions were satisfied: (i) artificial surfactant treatment did not improve the respiratory distress; (ii) prolonged rupture of membrane (PROM) continued for more than 5 days with oligohydramnios; and (iii) sufficient arterial oxygenation did not occur even after giving 100% oxygen, and more than 8 cm H(2)O of mean airway pressure was needed to maintain arterial oxygenation.

RESULTS

Nitric oxide inhalation improved arterial oxygenation rapidly and consistently in all eight infants with pulmonary hypoplasia. All eight iNO-treated infants survived longer than 28 days, while five of the 10 control infants died within 24 h of birth (P < 0.05). Before starting iNO, seven of the eight treated infants had shown persistent pulmonary hypertension, which was confirmed by echocardiography. No iNO-treated infant had IVH greater than grade 1, while one control infant had grade 2 IVH. All six long-term survivors in the iNO-treated group are developing normally, while only two of the control infants are developing normally as of February 2002.

CONCLUSIONS

The majority of the infants with pulmonary hypoplasia due to oligohydramnios had persistent pulmonary hypertension. iNO improved the arterial oxygenation and significantly improved the survival rate. A controlled study to determine whether iNO therapy improves the survival rate of preterm infants with pulmonary hypoplasia due to oligohydramnios is necessary.

摘要

背景

尽管吸入一氧化氮(iNO)疗法可改善足月儿的动脉氧合并降低体外膜肺氧合的使用率,但该疗法在早产儿中的疗效仍存在争议。本研究的目的是确定iNO疗法是否能提高因胎膜早破导致肺发育不全的极低出生体重儿的存活率。

方法

对因羊水过少导致肺发育不全且接受或未接受iNO治疗的极低出生体重儿进行回顾性对照研究(iNO治疗组,8例婴儿;对照组,10例婴儿)。若新生儿满足以下条件,则被认为因羊水过少导致肺发育不全:(i)人工表面活性剂治疗不能改善呼吸窘迫;(ii)胎膜早破(PROM)持续超过5天且伴有羊水过少;(iii)即使给予100%氧气后仍未出现足够的动脉氧合,且维持动脉氧合需要平均气道压超过8 cm H₂O。

结果

吸入一氧化氮使所有8例肺发育不全婴儿的动脉氧合迅速且持续改善。所有8例接受iNO治疗的婴儿存活时间均超过28天,而10例对照婴儿中有5例在出生后24小时内死亡(P < 0.05)。开始iNO治疗前,8例治疗婴儿中有7例经超声心动图证实存在持续性肺动脉高压。接受iNO治疗的婴儿无一例IVH大于1级,而1例对照婴儿出现2级IVH。iNO治疗组的6例长期存活者均发育正常,截至2002年2月,对照组中只有2例婴儿发育正常。

结论

大多数因羊水过少导致肺发育不全的婴儿存在持续性肺动脉高压。iNO改善了动脉氧合并显著提高了存活率。有必要进行对照研究以确定iNO疗法是否能提高因羊水过少导致肺发育不全的早产儿的存活率。

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