死亡延迟和慢性肺病增加:后表面活性剂时代死亡率降低的隐性成本。

K Wright
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引用次数: 0

摘要

为了确定1990年引入表面活性剂治疗前后通气的极低出生体重婴儿的发病率和死亡率的变化,我们回顾性研究了三级新生儿重症监护病房的婴儿。所有1984年1月1日至1997年12月31日住院的出生体重在1500g及以下的通气患者(76例转院患者除外)均纳入分析(N = 1336)。研究的主要结果包括死亡率、住院时间和无支气管肺发育不良的生存率。虽然使用表面活性剂后,出生体重大于750 g的婴儿死亡率和肺漏气率下降了50%以上(P < or = 0.026),但没有支气管肺发育不良的婴儿存活率也下降了(P < or = 0.034)。对于出生体重为751 ~ 1000 g的存活婴儿,表面活性剂后平均停留时间增加了16天(P = 0.008)。出生体重为750克或以下的婴儿在使用表面活性剂后死亡时的出生年龄也有所增加(P = 0.002)。对于出生体重小于等于1000 g的婴儿,表面活性剂后辅助通气的平均持续时间增加(+22%至32%,P < or = 0.005),经后36周支气管肺发育不良的发生率增加(+62%至162%,P < 0.001)。对于所有的婴儿,在表面活性剂后,菌血症的发生率、补充氧治疗的持续时间和出院的可能性都增加了(P <或= 0.011)。后表面活性剂时代死亡率降低的隐性好处可能被一些幸存者呼吸系统发病率的增加和一些非幸存者不受欢迎的死亡延长所抵消。我们推测,这些不良结果的最终成本可能大大超过表面上的成本效益新生儿表面活性剂治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Death postponement and increased chronic lung disease: the hidden costs of mortality reduction in the post-surfactant era.

To determine changes in the morbidity and mortality of ventilated, very low-birth-weight infants before and after the introduction of surfactant therapy in 1990, we retrospectively studied the infants in a tertiary neonatal intensive care unit. All ventilated patients admitted from January 1, 1984, to December 31, 1997, with birth weight of 1500 g or less, excluding 76 transferred to other hospitals, were included in the analysis (N = 1336). The primary outcomes studied included mortality, length of stay, and survival without bronchopulmonary dysplasia. Although post-surfactant mortality and pulmonary air leak for infants with birth weight greater than 750 g decreased more than 50% (P < or = .026), the proportion of infants surviving without bronchopulmonary dysplasia also decreased (P < or = .034). For surviving infants with birth weight of 751 to 1000 g, mean post-surfactant length of stay increased 16 days (P = .008). Postnatal age at death also increased in the post-surfactant period for infants with birth weight of 750 g or less (P = .002). For infants with birth weight of 1000 g or less, post-surfactant increases were seen in the mean duration of assisted ventilation (+22% to 32%, P < or = .005) and the incidence of bronchopulmonary dysplasia at 36 weeks' postmenstrual age (+62% to 162%, P < .001). For all infants, the incidence of bacteremia, duration of supplemental oxygen therapy, and likelihood of discharge on home oxygen were increased in the post-surfactant period (P < or = .011). The implicit benefits of mortality reduction in the post-surfactant era may be offset by increasing respiratory morbidity in some survivors and by an unwelcome prolongation of death for some nonsurvivors. We speculate that the ultimate costs of these undesirable outcomes may greatly surpass the ostensible cost benefits of neonatal surfactant therapy.

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