Ylikorkala O, Kauppila A, Kivinen S, Viinikka L
Br Med J (Clin Res Ed). 1982 Jul 24;285(6337):249-51. doi: 10.1136/bmj.285.6337.249.
Twenty-eight newly delivered mothers with inadequate lactation volunteered for a placebo-controlled double-blind trial of sulpiride 50 mg thrice daily for four weeks. Treatment was allocated at random, and serum prolactin concentrations and breast-milk yields were measured before and serially during the trial. Of the 26 women who completed the trial, 14 had taken sulpiride and 12 the placebo. In the sulpiride-treatment group the mean maternal serum prolactin concentration rose from 49.0 +/- SE 3.6 micrograms/l to a maximum of 402.1 +/0 43.2 micrograms/l at two weeks; in the placebo-treated group, however, the concentration fell during the trial (from 84.7 +/- 24.0 micrograms/l to 47.8 +/- 8.6 micrograms/l). Mean breast-milk yields also increased in the sulpiride-treatment group (by an average of 212-265 ml) and fell in the women given placebo. Of the 14 infants in the sulpiride-treatment group, four did not need supplementary feeds during the trial; in the control group, however, all infants continued to require such feeds. Infants in the sulpiride-treatment group gained significantly more weight than did the controls (p less than 0.05). Three women taking sulpiride complained of mild side effects, but none occurred in the infants. These findings suggest that sulpiride is an effective treatment for inadequate lactation in the puerperium.
28名产后泌乳不足的新妈妈自愿参加了一项安慰剂对照双盲试验,试验内容为每日三次服用50毫克舒必利,为期四周。治疗随机分配,在试验前及试验期间连续测量血清催乳素浓度和母乳产量。在完成试验的26名女性中,14人服用了舒必利,12人服用了安慰剂。在舒必利治疗组中,母亲血清催乳素平均浓度从49.0±标准误3.6微克/升升至两周时最高的402.1±43.2微克/升;然而,在安慰剂治疗组中,该浓度在试验期间下降(从84.7±24.0微克/升降至47.8±8.6微克/升)。舒必利治疗组的平均母乳产量也增加了(平均增加212 - 265毫升),而服用安慰剂的女性母乳产量下降。在舒必利治疗组的14名婴儿中,4名在试验期间不需要补充喂养;然而,在对照组中,所有婴儿仍需要补充喂养。舒必利治疗组的婴儿体重增加显著高于对照组(p<0.05)。三名服用舒必利的女性抱怨有轻微副作用,但婴儿均未出现副作用。这些发现表明,舒必利是治疗产后泌乳不足的有效药物。