J W Dudenhausen, G Kynast, A M Lange-Lindberg, E Saling
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引用次数: 19
摘要
60例长期服用非诺特罗(超过30毫克/天,持续14天)的患者157份羊水样本的卵磷脂含量;静脉输注时间大于7天)按Kynast and Saling薄层色谱法计算。这些卵磷脂水平与对照组进行统计学比较(Wilcoxon试验)。结果显示,长期模拟β治疗组卵磷脂水平显著降低,从33/0降至39/6 (33/0-34/6,p < 0.05;35/0-39/6, p < 0.01)。长期组中出现低于临界水平(3毫克Lec/100毫升羊水)的频率问题的答案似乎在临床上很重要。结果表明,在33/0到39/6的临界水平以下的值在长期β -模拟物治疗组中比在对照组中更常见。对此没有已知的解释。结论是,只有当羊水卵磷脂含量超过3 mg Lec/100 ml的临界限值时,才应停止在长期胎死腹中应用β -模拟物。
Influence of long-term beta-mimetic therapy on the lecithin content of amniotic fluid.
The lecithin content of 157 amniotic fluid samples taken from 60 patients who had been treated with Fenoterol over a long period of time (longer than 30 mg/daily per os for 14 days; intravenous infusion for longer than 7 days) was calculated thin-layer chromatographically according to Kynast and Saling. These lecithin levels were statistically compared with the levels in a control (Wilcoxon test). It emerged that the lecithin levels in the long-term beta-mimetic therapy group were significantly lower, i.e., from 33/0 to 39/6 (33/0-34/6, p less than 0.05; 35/0-39/6, p less than 0.01). The answer to the question how often levels occur in the long-term group which are below the as critical described level of 3 mg Lec/100 ml amniotic fluid appears to be clinically important. It is shown that values below the critical level from 33/0 to 39/6 are much more frequent in the long-term beta-mimetics therapy group than in the control group. There is no known explanation for this. It was concluded that the application of beta-mimetics in cases of long-term tocolysis should only be discontinued when the lecithin content of the amniotic fluid lies above the critical limit of 3 mg Lec/100 ml.