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血气值能否预测产前诊断的先天性膈疝中的肺发育不全?

Can blood gas values predict pulmonary hypoplasia in antenatally diagnosed congenital diaphragmatic hernia?

作者信息

Germain J F, Farnoux C, Pinquier D, Cortez A, Hartmann J F, Sibony O, de Lagausie P, Beaufils F

机构信息

Faculty of Medicine, Hôpital Robert Debré, Paris, France.

出版信息

J Pediatr Surg. 1996 Dec;31(12):1634-9. doi: 10.1016/s0022-3468(96)90036-6.

Abstract

The prognosis of antenatally diagnosed congenital diaphragmatic hernias (CDH) is clearly related to the degree of pulmonary hypoplasia (PH). After birth, controversies remain regarding the implementation of various therapies, especially the use of extracorporeal membrane oxygenation (ECMO). In the literature, the persistence of a Pao2 below 100 mm Hg and of Paco2 above 40 mm Hg despite optimal conventional therapy indicates poor prognosis. Therefore, since 1992, published and personal experiences led the authors to exclude CDH patients from ECMO when conventional therapy (including high-frequency oscillatory ventilation and nitric oxide) did not obtain Pao2 of above 80 mm Hg and Paco2 of below 60 mm Hg. The aim of this retrospective study is to determine whether blood gas results correlate with postmortem findings. Between July 1990 and July 1994, 32 cases of CDH were monitored antenatally and managed postnatally at the authors' institution. Six patients survived; 26 died, including one immediately at birth. Thirteen were treated by ECMO. Seventeen had a best Pao2 of above 80 mm Hg, including the six survivors. Fourteen did not reach this level, and none of them survived. Twenty-three infants underwent postmortem examination. PH was assessed using two criteria: (1) lung weight to body weight ratio (LW/BW) and (2) radial alveolar count (RAC). Two patients did not have hypoplasia (LW/BW > 0.018). Twenty-one patients had PH; 12 of them had an LW/BW ratio of less than .009; for 9, the LW/BW ratio was between .009 and .018, and the RAC (< 3.1) confirmed PH. All infants with a best Pao2 of less than 80 mm Hg had PH. Patients with a best Pao2 of greater than 80 mm Hg included two infants who died from complications without PH, eight infants with demonstrated PH, and the six survivors. In conclusion. (1) No infant with nonhypoplastic lungs has been deprived of ECMO by the authors' criteria. (2) Adequate values of blood gases may not eliminate PH. Therefore, this probably justifies starting ECMO when conventional therapy fails. (3) Conversely, permanent poor values of Pao2 allowed the prediction of PH in all cases. Such patients probably can be excluded from ECMO treatment.

摘要

产前诊断的先天性膈疝(CDH)的预后显然与肺发育不全(PH)的程度相关。出生后,关于各种治疗方法的实施仍存在争议,尤其是体外膜肺氧合(ECMO)的使用。在文献中,尽管进行了最佳的传统治疗,但动脉血氧分压(Pao2)持续低于100 mmHg且动脉血二氧化碳分压(Paco2)高于40 mmHg表明预后不良。因此,自1992年以来,已发表的文献和个人经验使作者们在传统治疗(包括高频振荡通气和一氧化氮)未能使Pao2高于80 mmHg且Paco2低于60 mmHg时,将CDH患者排除在ECMO治疗之外。这项回顾性研究的目的是确定血气结果是否与尸检结果相关。1990年7月至1994年7月期间,作者所在机构对32例CDH患者进行了产前监测和产后管理。6例患者存活;26例死亡,其中1例出生时即刻死亡。13例接受了ECMO治疗。17例患者的最佳Pao2高于80 mmHg,包括6例幸存者。14例未达到这一水平,且无一存活。23例婴儿接受了尸检。使用两个标准评估肺发育不全:(1)肺重量与体重比(LW/BW)和(2)肺泡计数(RAC)。2例患者没有肺发育不全(LW/BW > 0.018)。21例患者有肺发育不全;其中12例的LW/BW比值小于0.009;9例的LW/BW比值在0.009至0.018之间,且RAC(< 3.1)证实有肺发育不全。所有最佳Pao2低于80 mmHg的婴儿都有肺发育不全。最佳Pao2高于80 mmHg的患者包括2例死于无肺发育不全并发症的婴儿、8例有肺发育不全表现的婴儿和6例幸存者。总之,(1)按照作者的标准,没有肺发育正常的婴儿被排除在ECMO治疗之外。(2)足够的血气值可能无法消除肺发育不全。因此,这可能证明在传统治疗失败时启动ECMO是合理的。(3)相反,持续的低Pao2值在所有病例中都可预测肺发育不全。这类患者可能可被排除在ECMO治疗之外。

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