Foong Siew Cheng, Tan May Loong, Foong Wai Cheng, Marasco Lisa A, Ho Jacqueline J, Ong Joo Howe
Department of Paediatrics, RCSI & UCD Malaysia Campus (formerly Penang Medical College), George Town, Malaysia.
Santa Barbara County Public Health Department, Nutrition Services/Breastfeeding Program, Santa Maria, California, USA.
Cochrane Database Syst Rev. 2020 May 18;5(5):CD011505. doi: 10.1002/14651858.CD011505.pub2.
Many women express concern about their ability to produce enough milk, and insufficient milk is frequently cited as the reason for supplementation and early termination of breastfeeding. When addressing this concern, it is important first to consider the influence of maternal and neonatal health, infant suck, proper latch, and feeding frequency on milk production, and that steps be taken to correct or compensate for any contributing issues. Oral galactagogues are substances that stimulate milk production. They may be pharmacological or non-pharmacological (natural). Natural galactagogues are usually botanical or other food agents. The choice between pharmacological or natural galactagogues is often influenced by familiarity and local customs. Evidence for the possible benefits and harms of galactagogues is important for making an informed decision on their use.
To assess the effect of oral galactagogues for increasing milk production in non-hospitalised breastfeeding mother-term infant pairs.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register, ClinicalTrials.gov, the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP), Health Research and Development Network - Phillippines (HERDIN), Natural Products Alert (Napralert), the personal reference collection of author LM, and reference lists of retrieved studies (4 November 2019).
We included randomised controlled trials (RCTs) and quasi-RCTs (including published abstracts) comparing oral galactagogues with placebo, no treatment, or another oral galactagogue in mothers breastfeeding healthy term infants. We also included cluster-randomised trials but excluded cross-over trials.
We used standard Cochrane Pregnancy and Childbirth methods for data collection and analysis. Two to four review authors independently selected the studies, assessed the risk of bias, extracted data for analysis and checked accuracy. Where necessary, we contacted the study authors for clarification.
Forty-one RCTs involving 3005 mothers and 3006 infants from at least 17 countries met the inclusion criteria. Studies were conducted either in hospitals immediately postpartum or in the community. There was considerable variation in mothers, particularly in parity and whether or not they had lactation insufficiency. Infants' ages at commencement of the studies ranged from newborn to 6 months. The overall certainty of evidence was low to very low because of high risk of biases (mainly due to lack of blinding), substantial clinical and statistical heterogeneity, and imprecision of measurements. Pharmacological galactagogues Nine studies compared a pharmacological galactagogue (domperidone, metoclopramide, sulpiride, thyrotropin-releasing hormone) with placebo or no treatment. The primary outcome of proportion of mothers who continued breastfeeding at 3, 4 and 6 months was not reported. Only one study (metoclopramide) reported on the outcome of infant weight, finding little or no difference (mean difference (MD) 23.0 grams, 95% confidence interval (CI) -47.71 to 93.71; 1 study, 20 participants; low-certainty evidence). Three studies (metoclopramide, domperidone, sulpiride) reported on milk volume, finding pharmacological galactagogues may increase milk volume (MD 63.82 mL, 95% CI 25.91 to 101.72; I² = 34%; 3 studies, 151 participants; low-certainty evidence). Subgroup analysis indicates there may be increased milk volume with each drug, but with varying CIs. There was limited reporting of adverse effects, none of which could be meta-analysed. Where reported, they were limited to minor complaints, such as tiredness, nausea, headache and dry mouth (very low-certainty evidence). No adverse effects were reported for infants. Natural galactagogues Twenty-seven studies compared natural oral galactagogues (banana flower, fennel, fenugreek, ginger, ixbut, levant cotton, moringa, palm dates, pork knuckle, shatavari, silymarin, torbangun leaves or other natural mixtures) with placebo or no treatment. One study (Mother's Milk Tea) reported breastfeeding rates at six months with a concluding statement of "no significant difference" (no data and no measure of significance provided, 60 participants, very low-certainty evidence). Three studies (fennel, fenugreek, moringa, mixed botanical tea) reported infant weight but could not be meta-analysed due to substantial clinical and statistical heterogeneity (I = 60%, 275 participants, very low-certainty evidence). Subgroup analysis shows we are very uncertain whether fennel or fenugreek improves infant weight, whereas moringa and mixed botanical tea may increase infant weight compared to placebo. Thirteen studies (Bu Xue Sheng Ru, Chanbao, Cui Ru, banana flower, fenugreek, ginger, moringa, fenugreek, ginger and turmeric mix, ixbut, mixed botanical tea, Sheng Ru He Ji, silymarin, Xian Tong Ru, palm dates; 962 participants) reported on milk volume, but meta-analysis was not possible due to substantial heterogeneity (I = 99%). The subgroup analysis for each intervention suggested either benefit or little or no difference (very low-certainty evidence). There was limited reporting of adverse effects, none of which could be meta-analysed. Where reported, they were limited to minor complaints such as mothers with urine that smelled like maple syrup and urticaria in infants (very low-certainty evidence). Galactagogue versus galactagogue Eight studies (Chanbao; Bue Xue Sheng Ru, domperidone, moringa, fenugreek, palm dates, torbangun, moloco, Mu Er Wu You, Kun Yuan Tong Ru) compared one oral galactagogue with another. We were unable to perform meta-analysis because there was only one small study for each match-up, so we do not know if one galactagogue is better than another for any outcome.
AUTHORS' CONCLUSIONS: Due to extremely limited, very low certainty evidence, we do not know whether galactagogues have any effect on proportion of mothers who continued breastfeeding at 3, 4 and 6 months. There is low-certainty evidence that pharmacological galactagogues may increase milk volume. There is some evidence from subgroup analyses that natural galactagogues may benefit infant weight and milk volume in mothers with healthy, term infants, but due to substantial heterogeneity of the studies, imprecision of measurements and incomplete reporting, we are very uncertain about the magnitude of the effect. We are also uncertain if one galactagogue performs better than another. With limited data on adverse effects, we are uncertain if there are any concerning adverse effects with any particular galactagogue; those reported were minor complaints. High-quality RCTs on the efficacy and safety of galactagogues are urgently needed. A set of core outcomes to standardise infant weight and milk volume measurement is also needed, as well as a strong basis for the dose and dosage form used.
许多女性对自身产奶量表示担忧,而乳汁不足常被视为添加配方奶及提前终止母乳喂养的原因。在解决这一担忧时,首先要考虑母亲和新生儿健康、婴儿吸吮、正确含接以及喂养频率对乳汁分泌的影响,并采取措施纠正或弥补任何相关问题。口服催乳剂是刺激乳汁分泌的物质。它们可以是药物性的或非药物性的(天然的)。天然催乳剂通常是植物性或其他食物成分。在药物性或天然催乳剂之间的选择通常受熟悉程度和当地习俗影响。了解催乳剂可能的益处和危害的证据对于明智地决定是否使用它们很重要。
评估口服催乳剂对非住院的母乳喂养母婴对增加乳汁分泌量的效果。
我们检索了Cochrane妊娠与分娩组试验注册库、ClinicalTrials.gov、世界卫生组织(WHO)国际临床试验注册平台(ICTRP)、菲律宾卫生研究与发展网络(HERDIN)、天然产物警报(Napralert)、作者LM的个人参考文献集以及检索到的研究的参考文献列表(2019年11月4日)。
我们纳入了随机对照试验(RCT)和半随机对照试验(包括已发表的摘要),这些试验比较了口服催乳剂与安慰剂、不治疗或另一种口服催乳剂在母乳喂养足月健康婴儿的母亲中的效果。我们还纳入了整群随机试验,但排除了交叉试验。
我们采用Cochrane妊娠与分娩组的标准方法进行数据收集和分析。两至四位综述作者独立选择研究、评估偏倚风险、提取分析数据并检查准确性。必要时,我们联系研究作者进行澄清。
41项RCT涉及来自至少17个国家的3005名母亲和3006名婴儿,符合纳入标准。研究在产后立即在医院或社区进行。母亲的情况差异很大,特别是在胎次以及是否有泌乳不足方面。研究开始时婴儿的年龄从新生儿到6个月不等。由于偏倚风险高(主要是由于缺乏盲法)、大量的临床和统计异质性以及测量的不精确性,证据的总体确定性为低至极低。
9项研究比较了一种药物性催乳剂(多潘立酮、甲氧氯普胺、舒必利、促甲状腺激素释放激素)与安慰剂或不治疗。未报告3、4和6个月时继续母乳喂养的母亲比例这一主要结局。只有一项研究(甲氧氯普胺)报告了婴儿体重结局,发现几乎没有差异(平均差(MD)23.0克,95%置信区间(CI)-47.71至93.71;1项研究,20名参与者;低确定性证据)。3项研究(甲氧氯普胺、多潘立酮、舒必利)报告了乳汁量,发现药物性催乳剂可能增加乳汁量(MD 63.82 mL,95%CI 25.91至101.72;I² = 34%;3项研究,151名参与者;低确定性证据)。亚组分析表明每种药物可能都增加了乳汁量,但置信区间不同。不良反应的报告有限,且均无法进行荟萃分析。报告的不良反应仅限于轻微不适,如疲倦、恶心、头痛和口干(极低确定性证据)。未报告对婴儿有不良反应。
27项研究比较了天然口服催乳剂(香蕉花、茴香、葫芦巴、生姜、ixbut、棉葵、辣木、椰枣、猪脚、沙塔瓦里、水飞蓟素、torbangun叶或其他天然混合物)与安慰剂或不治疗。一项研究(妈妈奶茶)报告了6个月时的母乳喂养率,结论为“无显著差异”(未提供数据和显著性测量;60名参与者,极低确定性证据)。3项研究(茴香、葫芦巴、辣木、混合植物茶)报告了婴儿体重,但由于大量的临床和统计异质性(I = 60%,275名参与者,极低确定性证据)无法进行荟萃分析。亚组分析表明,我们非常不确定茴香或葫芦巴是否能改善婴儿体重,而与安慰剂相比,辣木和混合植物茶可能增加婴儿体重。13项研究(补血生乳、产宝、催乳、香蕉花、葫芦巴、生姜、辣木、葫芦巴、生姜和姜黄混合物、ixbut、混合植物茶、生乳合剂、水飞蓟素、仙通乳、椰枣;962名参与者)报告了乳汁量,但由于大量异质性(I = 99%)无法进行荟萃分析。每种干预措施的亚组分析表明可能有益或几乎没有差异(极低确定性证据)。不良反应的报告有限,且均无法进行荟萃分析。报告的不良反应仅限于轻微不适,如母亲尿液有枫糖浆味和婴儿荨麻疹(极低确定性证据)。
8项研究(产宝;补血生乳、多潘立酮、辣木、葫芦巴、椰枣、torbangun、moloco、母乳无忧、坤源通乳)比较了一种口服催乳剂与另一种。我们无法进行荟萃分析,因为每种配对只有一项小型研究,所以我们不知道对于任何结局一种催乳剂是否比另一种更好。
由于证据极其有限且确定性极低,我们不知道催乳剂对3、4和6个月时继续母乳喂养的母亲比例是否有任何影响。有低确定性证据表明药物性催乳剂可能增加乳汁量。亚组分析有一些证据表明天然催乳剂可能对健康足月婴儿母亲的婴儿体重和乳汁量有益,但由于研究的大量异质性、测量的不精确性和报告的不完整性,我们对效果的大小非常不确定。我们也不确定一种催乳剂是否比另一种效果更好。由于不良反应的数据有限,我们不确定任何特定的催乳剂是否有令人担忧的不良反应;报告的都是轻微不适。迫切需要关于催乳剂疗效和安全性的高质量RCT。还需要一套标准化婴儿体重和乳汁量测量的核心结局,以及所用剂量和剂型的坚实依据。