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预防性给予肺表面活性物质对新生儿呼吸窘迫综合征的保护和治疗作用

[Protective and curative effects of prophylactic administration of pulmonary surfactant on neonatal respiratory distress syndrome].

作者信息

Chu Gui-lan, Wang Jing, Xin Yue, Zheng Jun, Zheng Rong-xiu, Bi Dao-zhuo

机构信息

General Hospital of Tianjin Medical University, Tianjin 300052, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2006 Apr 4;86(13):876-80.

Abstract

OBJECTIVE

To evaluate the protective and curative effects of prophylactic administration of pulmonary surfactant (PS) on neonatal respiratory distress syndrome (NRDS).

METHODS

One hundred neonates aged 0.5 h after birth, with the gestational age < 32 w, birth weight < 1500 g, and number of gastric, stable microbubble < or = 7/mm(2) by gastric stable microbubble test (SMT), but without clinical or radiological manifestations of RDS at the admission, were randomly divided into 2 equal groups: prophylactic group (PG), receiving curosurf, a product of PS, immediately after admission; and non-prophylactic group (N-PG), receiving curosurf only after development of RDS.

RESULTS

One hour after the administration of PS, the PaO(2), a/APO(2), pH, and PaO(2) of the PG group were 86.2 mm Hg +/- 8.1 mm Hg, 0.30 +/- 0.04, 7.38 +/- 0.06, and 178 +/- 37, all significantly higher than those of the non-PG group (all P < 0.01), and the PaCO(2) of the PG group was 37.3 mm Hg +/- 9.8 mm Hg, significantly lower than that of the non-PG group (53.6 mm Hg +/- 11.1 mm Hg, P < 0.01). In comparison with the level before the administration of PS (0.75 +/- 0.06), the level of FiO(2) of the 47 pediatric patients receiving mechanical ventilation decreased after the administration of curosurf time-dependently, e.g., was 0.50 +/- 0.09, 0.34 +/- 0.06, and 0.25 +/- 0.07 8, 48, and 96 hours after the administration. In comparison with the level before the administration of curosurf 9.0 +/- 1.0 cm H2O, the level of mean airway pressure (MAP) decreased time-dependently after the administration, e.g., were 7.5 +/- 0.8 and 6.0 +/- 0.3 48 and 96 hours after the administration (all P < 0.01). Compared with that before the administration of curosurf (3.02 +/- 0.2), the X-ray chest score decreased time-dependently after the administration of curosurf, e.g., were 1.89 +/- 0.34, 1.82 +/- 0.33, and 1.17 +/- 0.42 6, 12, and 72 hours after the administration (all P < 0.01). The RDS rate of the PG group was 30%, significantly lower than that of the non-PG group (P < 0.01). The severe case rate of the PG group was 20%, significantly lower than that of the N-PG group (53%, P = 0.01). The mortally of the PG group was 0, significantly lower than that of the non-PG group (P < 0.05). The total times of supplemental oxygen administration, assisted ventilation and hospitalization of the 47 patients with RDS in the PG group were significantly shortened compared with the RDS patients in the N-PG group [(3.6 +/- 1.7) d vs. (5.9 +/- 3.6) d, P < 0.05; (8.6 +/- 5.5 d vs. (14.1 +/- 6.2) d, P < 0.01; and (20.5 +/- 10.0) d vs. (32.8 +/- 17.8) d, P < 0.05).

CONCLUSION

Prophylactic administration of PS to the preterm neonates with high risk of RDS effectively decreases the incidence of RDS, development of severe cases and mortality, shorten the disease course, the duration of supplemental oxygen administration and assisted ventilation, thus decreasing the potential morbidity associated with long-term oxygen supplement and assisted ventilation.

摘要

目的

评估预防性应用肺表面活性物质(PS)对新生儿呼吸窘迫综合征(NRDS)的防治效果。

方法

选取出生后0.5小时的100例新生儿,胎龄<32周,出生体重<1500g,经胃稳定微泡试验(SMT)胃内稳定微泡数<或=7/mm(2),入院时无RDS临床或影像学表现,随机分为2组:预防组(PG),入院后立即给予珂立苏(PS产品);非预防组(N-PG),仅在发生RDS后给予珂立苏。

结果

PS给药后1小时,PG组的PaO(2)、a/APO(2)、pH和PaO(2)分别为86.2mmHg±8.1mmHg、0.30±0.04、7.38±0.06和178±37,均显著高于非PG组(均P<0.01),PG组的PaCO(2)为37.3mmHg±9.8mmHg,显著低于非PG组(53.6mmHg±11.1mmHg,P<0.01)。与PS给药前水平(0.75±0.06)相比,47例接受机械通气的患儿给予珂立苏后FiO(2)水平随时间下降,如给药后8、48和96小时分别为0.50±0.09、0.34±0.06和0.25±0.07。与给予珂立苏前水平9.0±1.0cmH2O相比,给药后平均气道压(MAP)随时间下降,如给药后48和96小时分别为7.5±0.8和6.0±0.3(均P<0.01)。与给予珂立苏前(3.02±0.2)相比,给予珂立苏后胸部X线评分随时间下降,如给药后6、12和72小时分别为1.89±0.34、1.82±0.33和1.17±0.42(均P<0.01)。PG组的RDS发生率为30%,显著低于非PG组(P<0.01)。PG组的重症发生率为20%,显著低于N-PG组(53%,P=0.01)。PG组的死亡率为0,显著低于非PG组(P<0.05)。PG组47例RDS患者的总吸氧时间、辅助通气时间和住院时间与N-PG组的RDS患者相比显著缩短[(3.6±1.7)天对(5.9±3.6)天,P<0.05;(8.6±5.5)天对(14.1±6.2)天,P<0.01;(20.5±10.0)天对(32.8±17.8)天,P<0.05]。

结论

对有RDS高危风险的早产儿预防性应用PS可有效降低RDS发生率、重症发生率和死亡率,缩短病程、吸氧时间和辅助通气时间,从而降低与长期吸氧和辅助通气相关的潜在发病率。

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