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安抚奶嘴使用与母乳喂养、婴儿猝死综合征、感染及牙列不齐之间的关联。

Association between pacifier use and breast-feeding, sudden infant death syndrome, infection and dental malocclusion.

作者信息

Callaghan Ann, Kendall Garth, Lock Christine, Mahony Anne, Payne Jan, Verrier Leanda

机构信息

1Telethon Institute for Child Health Research, 2School of Nursing and Midwifery, Curtin University of Technology, and 3Health Department of Western Australia, Perth, Western Australia, Australia.

出版信息

JBI Libr Syst Rev. 2005;3(6):1-33. doi: 10.11124/01938924-200503060-00001.

Abstract

OBJECTIVE

To critically review all literature related to pacifier use for full-term healthy infants and young children.The specific review questions addressed are:What is the evidence of adverse and/or positive outcomes of pacifier use in infancy and childhood in relation to each of the following subtopics: INCLUSION CRITERIA: Specific criteria were used to determine which studies would be included in the review: (i) the types of participants; (ii) the types of research design; and (iii) the types of outcome measures. To be included a study has to meet all criteria.The participants included in the review were healthy term infants and healthy children up to the age of 16 years. Studies that focused on preterm infants, and infants and young children with serious illness or congenital malformations were excluded. However, some total population studies did include these children.It became evident early in the review process that very few randomised controlled trials had been conducted. A decision was made to include observational epidemiological designs, specifically prospective cohort studies and, in the case of sudden infant death syndrome research, case-control studies. Purely descriptive and cross-sectional studies were excluded, as were qualitative studies and all other forms of evidence.A number of criteria have been proposed to establish causation in the scientific and medical literature. These key criteria were applied in the review process and are described as follows: (i) consistency and unbiasedness of findings; (ii) strength of association; (iii) temporal sequence; (iv) dose-response relationship; (v) specificity; (vi) coherence with biological background and previous knowledge; (vii) biological plausibility; and (viii) experimental evidence.Studies that did not meet the requirement of appropriate temporal sequencing of events and studies that did not present an estimate of the strength of association were not included in the final review.Our specific interest was pacifier use related to:Studies that examined pacifier use related to procedural pain relief were excluded. Studies that examined the relationship between pacifier use and gastro-oesophageal reflux were also excluded as this information has been recently presented as a systematic review.

SEARCH STRATEGY

The review comprised published and unpublished research literature. The search was restricted to reports published in English, Spanish and German. The time period covered research published from January 1960 to October 2003. A protocol developed by New Zealand Health Technology Assessment was used to guide the search process. The search comprised bibliographic databases, citation searching, other evidence-based and guidelines sites, government documents, books and reports, professional websites, national associations, hand search, contacting national/international experts and general internet searching.

ASSESSMENT OF QUALITY

All studies identified during the database search were assessed for relevance to the review based on the information provided in the title, abstract and descriptor/MeSH terms, and a full report was retrieved for all studies that met the inclusion criteria. Studies identified from reference list searches were assessed for relevance based on the study title. Keywords included: dummy, dummies, pacifier(s), soother(s), comforter(s), non-nutritive sucking, infant, child, infant care.Initially, studies were reviewed for inclusion by pairs of principal investigators. Authorship of articles was not concealed from the reviewers. Next, the methodological quality of included articles was assessed independently by groups of three or more principal investigators and clinicians using a checklist. All 20 studies that were accepted met minimum set criteria, but few passed without some methodological concern.

DATA EXTRACTION

To meet the requirements of the Joanna Briggs Institute, reasons for acceptance and non-acceptance at each phase were clearly documented. An assessment protocol and report form was developed for each of the three phases of review. The first form was created to record investigators' evaluations of studies included in the initial review. Those studies that failed to meet strict inclusion criteria were excluded at this point. A second form was designed to facilitate an in-depth critique of epidemiological study methodology. The checklist was pilot tested and adjustments were made before reviewers were trained in its use. When reviewers could not agree on an assessment, it was passed to additional reviewers and discussed until a consensus was reached. At this stage, studies other than cohort, case-control and randomised controlled trials were excluded. Issues of clarification were also addressed at this point. The final phase was that of integration. This phase, undertaken by the principal investigators, was assisted by the production of data extraction tables. Through a process of trial and error, a framework was formulated that adequately summarised the key elements of the studies. This information was tabulated under the following headings: authors/setting, design, exposure/outcome, confounders controlled, analysis and main findings.

RESULTS

With regard to the breast-feeding outcome, 10 studies met the inclusion criteria, comprising two randomised controlled trials and eight cohort studies. The research was conducted between 1995 and 2003 in a wide variety of settings involving research participants from diverse socioeconomic and cultural backgrounds. Information regarding exposure and outcome status, and potential confounding factors was obtained from: antenatal and postnatal records; interviews before discharge from obstetric/midwifery care; post-discharge interviews; and post-discharge postal and telephone surveys. Both the level of contact and the frequency of contact with the informant, the child's mother, differed widely. Pacifier use was defined and measured inconsistently, possibly because few studies were initiated expressly to investigate its relationship with breast-feeding. Completeness of follow-up was addressed, but missing data were not uniformly identified and explained. When comparisons were made between participants and non-participants there was some evidence of differential loss and a bias towards families in higher socioeconomic groups. Multivariate analysis was undertaken in the majority of studies, with some including a large number of sociodemographic, obstetric and infant covariates and others including just maternal age and education.As might be expected given the inconsistency of definition and measurement, the relationship between pacifier use and breast-feeding was expressed in many different ways and a meta-analysis was not appropriate. In summary, only one study did not report a negative association between pacifier use and breast-feeding duration or exclusivity. Results indicate an increase in risk for a reduced overall duration of breast-feeding from 20% to almost threefold. The data suggest that very infrequent use may not have any overall negative impact on breast-feeding outcomes.Six sudden infant death syndrome case-control studies met the criteria for inclusion. The research was conducted with information gathered between 1984 and 1999 in Norway, UK, New Zealand, the Netherlands and USA. Exposure information was obtained from a variety of sources including: hospital and antenatal records, death scene investigation, and interview and questionnaire. Information for cases was sought within 2 days after death, within 2-4 weeks after death and in one study between 3 and 11 years after death. Information for controls was sought from as early as 4 days of a nominated sudden infant death syndrome case, to between 1 and 7 weeks from the case date, and again in one study some 3-11 years later. In the majority of the studies case ascertainment was determined by post-mortem. Pacifier use was again defined and measured somewhat inconsistently. All studies controlled for confounding factors by matching and/or using multivariate analysis. Generally, antenatal and postnatal factors, as well as infant care practices, and maternal, family and socioeconomic issues were considered.All five studies reporting multivariate results found significantly fewer sudden infant death syndrome cases used a pacifier compared with controls. That is, pacifier use was associated with a reduced incidence of sudden infant death syndrome. These results indicate that the risk of sudden infant death syndrome for infants who did not use a pacifier in the last or reference sleep was at least twice, and possibly five times, that of infants who did use a pacifier.Three studies reported a moderately sized positive association between pacifier use and a variety of infections. Conversely, one study found no positive association between pacifier use at 15 months of age and a range of infections experienced between the ages of 6 and 18 months. Given the limited number of studies available and the variability of results, no meaningful conclusions could be drawn.Five cohort studies and one case-control study focused on the relationship between pacifier use and dental malocclusion. Not one of these studies reported a measure of association, such as an estimate of relative risk. It was therefore not possible to include these studies in the final review.Implications for practice It is intended that this review be used as the basis of a 'best practice guideline', to make health professionals aware of the research evidence concerning these health and developmental consequences of pacifier use, because parents need clear information on which they can base child care decisions. With regard to the association between pacifier use and infection and dental malocclusion it was found that, due to the paucity of epidemiological studies, no meaningful conclusion can be drawn. There is clearly a need for more epidemiological research with regard to these two outcomes. The evidence for a relationship between pacifier use and sudden infant death syndrome is consistent, while the exact mechanism of the effect is not well understood. As to breast-feeding, research evidence shows that pacifier use in infancy is associated with a shorter duration and non-exclusivity. It is plausible that pacifier use causes babies to breast-feed less, but a causal relationship has not been irrefutably proven.Because breast-feeding confers an important advantage on all children and the incidence of sudden infant death syndrome is very low, it is recommended that health professionals generally advise parents against pacifier use, while taking into account individual circumstances.

摘要

目的

严格审查与足月健康婴幼儿使用安抚奶嘴相关的所有文献。所涉及的具体审查问题如下:在婴幼儿期使用安抚奶嘴,就以下每个子主题而言,其产生不良和/或积极结果的证据是什么:纳入标准:使用特定标准来确定哪些研究将被纳入审查:(i)参与者类型;(ii)研究设计类型;(iii)结果测量类型。要纳入一项研究必须满足所有标准。审查纳入的参与者为足月健康婴儿和16岁以下的健康儿童。聚焦于早产儿以及患有严重疾病或先天性畸形的婴幼儿的研究被排除。然而,一些总体人群研究确实纳入了这些儿童。在审查过程早期就明显发现,很少有随机对照试验。于是决定纳入观察性流行病学设计,特别是前瞻性队列研究,以及在婴儿猝死综合征研究方面的病例对照研究。纯粹的描述性和横断面研究被排除,定性研究及所有其他形式的证据也被排除。科学和医学文献中已提出若干标准来确立因果关系。这些关键标准在审查过程中得到应用,具体如下:(i)研究结果的一致性和无偏性;(ii)关联强度;(iii)时间顺序;(iv)剂量反应关系;(v)特异性;(vi)与生物学背景和先前知识的一致性;(vii)生物学合理性;(viii)实验证据。未满足事件适当时间顺序要求的研究以及未给出关联强度估计值的研究未被纳入最终审查。我们特别关注的是与以下方面相关的安抚奶嘴使用情况:审查中排除了研究安抚奶嘴用于缓解程序性疼痛的相关研究。审查中也排除了研究安抚奶嘴使用与胃食管反流之间关系的研究,因为该信息最近已作为一项系统评价呈现。

检索策略

该审查涵盖已发表和未发表的研究文献。检索限于以英文、西班牙文和德文发表的报告。时间范围涵盖1960年1月至2003年10月发表的研究。使用新西兰卫生技术评估制定的方案来指导检索过程。检索包括书目数据库、引文检索、其他循证和指南网站、政府文件、书籍和报告、专业网站、全国性协会、手工检索、联系国家/国际专家以及一般互联网搜索。

质量评估

根据标题、摘要和描述符/医学主题词中提供的信息,对数据库搜索过程中识别出的所有研究进行相关性评估,对于所有符合纳入标准的研究均检索完整报告。从参考文献列表搜索中识别出的研究根据研究标题评估相关性。关键词包括:安抚奶嘴、安抚奶嘴类、橡皮奶头、抚慰奶嘴、安慰奶嘴、非营养性吸吮、婴儿、儿童、婴儿护理。最初,由两位主要研究者对研究进行纳入审查。文章作者身份未向审查者隐瞒。接下来,由三名或更多主要研究者和临床医生组成的小组使用一份清单独立评估纳入文章的方法学质量。所有被接受的20项研究均符合最低设定标准,但很少有研究在方法学上毫无问题。

数据提取

为满足乔安娜·布里格斯研究所的要求,在每个阶段接受和不接受的原因都有明确记录。针对审查的三个阶段分别制定了评估方案和报告表。第一个表格用于记录研究者对初步审查中纳入研究的评估。此时,那些未达到严格纳入标准的研究被排除。第二个表格旨在便于对流行病学研究方法进行深入批判。该清单经过预试验,并在培训审查者使用之前进行了调整。当审查者无法就评估达成一致时,将其提交给其他审查者并进行讨论,直至达成共识。在此阶段,除队列研究、病例对照研究和随机对照试验之外的其他研究被排除。此时还处理了澄清问题。最后一个阶段是整合阶段。这个阶段由主要研究者进行,在制作数据提取表的协助下完成。通过反复试验,制定了一个框架,充分总结了研究的关键要素。这些信息按照以下标题制成表格:作者/研究背景、设计、暴露/结果、控制的混杂因素、分析和主要发现。

结果

关于母乳喂养结果,10项研究符合纳入标准,包括两项随机对照试验和八项队列研究。该研究于1995年至2003年期间在各种环境中进行,研究参与者来自不同的社会经济和文化背景。关于暴露和结果状态以及潜在混杂因素的信息来自:产前和产后记录;产科/助产护理出院前的访谈;出院后的访谈;以及出院后的邮寄和电话调查。与提供信息者即孩子母亲的接触程度和频率差异很大。安抚奶嘴的使用定义和测量不一致,可能是因为很少有研究专门为调查其与母乳喂养的关系而开展。随访的完整性得到了关注,但缺失数据并未得到统一识别和解释。当对参与者和非参与者进行比较时,有证据表明存在差异损失,且偏向社会经济地位较高的家庭。大多数研究进行了多变量分析,一些研究纳入了大量社会人口学、产科和婴儿协变量,而另一些研究仅纳入了母亲年龄和教育程度。鉴于定义和测量的不一致,安抚奶嘴使用与母乳喂养之间的关系以多种不同方式呈现,因此不适合进行荟萃分析。总之,只有一项研究未报告安抚奶嘴使用与母乳喂养持续时间或排他性之间的负相关关系。结果表明,母乳喂养总持续时间减少的风险增加了20%至近三倍。数据表明,极少使用可能对母乳喂养结果没有任何总体负面影响。六项婴儿猝死综合征病例对照研究符合纳入标准。该研究利用1984年至1999年期间在挪威、英国、新西兰、荷兰和美国收集的信息进行。暴露信息来自多种来源,包括:医院和产前记录、死亡现场调查以及访谈和问卷。病例信息在死亡后2天内、死亡后2 - 4周内以及一项研究中在死亡后3至11年内获取。对照信息最早在指定的婴儿猝死综合征病例出现后4天内、病例日期后1至7周内以及一项研究中约3至11年后获取。在大多数研究中,病例确诊通过尸检确定。安抚奶嘴的使用再次定义和测量得有些不一致。所有研究通过匹配和/或使用多变量分析来控制混杂因素。一般来说,考虑了产前和产后因素、婴儿护理习惯以及母亲、家庭和社会经济问题。所有五项报告多变量结果的研究均发现,与对照组相比,使用安抚奶嘴的婴儿猝死综合征病例显著更少。也就是说,安抚奶嘴的使用与婴儿猝死综合征发病率降低相关。这些结果表明,在最后一次或参考睡眠中未使用安抚奶嘴的婴儿发生婴儿猝死综合征的风险至少是使用安抚奶嘴婴儿的两倍,甚至可能是五倍。三项研究报告了安抚奶嘴使用与多种感染之间存在中等程度的正相关。相反,一项研究发现15个月大时使用安抚奶嘴与6至18个月期间经历的一系列感染之间没有正相关。鉴于现有研究数量有限且结果存在差异,无法得出有意义的结论。五项队列研究和一项病例对照研究聚焦于安抚奶嘴使用与牙齿咬合不正之间的关系。这些研究均未报告关联度量,如相对风险估计值。因此,无法将这些研究纳入最终审查。对实践的启示 本综述旨在作为“最佳实践指南”的基础,使卫生专业人员了解关于安抚奶嘴使用对这些健康和发育影响的研究证据,因为父母需要明确的信息来做出儿童护理决策。关于安抚奶嘴使用与感染和牙齿咬合不正之间的关联,发现由于流行病学研究匮乏,无法得出有意义的结论。显然需要针对这两个结果开展更多的流行病学研究。安抚奶嘴使用与婴儿猝死综合征之间关系的证据是一致的,但其确切作用机制尚不清楚。至于母乳喂养,研究证据表明婴儿期使用安抚奶嘴与较短的持续时间和非排他性相关。安抚奶嘴使用可能导致婴儿母乳喂养减少,但因果关系尚未得到确凿证明。由于母乳喂养对所有儿童都具有重要优势,且婴儿猝死综合征的发病率非常低,建议卫生专业人员在考虑个体情况的同时,一般建议父母不要使用安抚奶嘴。

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