Barlow Jane, Bennett Cathy, Midgley Nick, Larkin Soili K, Wei Yinghui
Division of Mental Health and Wellbeing, Warwick Medical School, University of Warwick, Gibbett Hill Road, Coventry, UK, CV4 7LF.
Cochrane Database Syst Rev. 2015 Jan 8;1(1):CD010534. doi: 10.1002/14651858.CD010534.pub2.
Parent-infant psychotherapy (PIP) is a dyadic intervention that works with parent and infant together, with the aim of improving the parent-infant relationship and promoting infant attachment and optimal infant development. PIP aims to achieve this by targeting the mother's view of her infant, which may be affected by her own experiences, and linking them to her current relationship to her child, in order to improve the parent-infant relationship directly.
We searched the following electronic databases on 13 January 2014: Cochrane Central Register of Controlled Trials (CENTRAL, 2014, Issue 1), Ovid MEDLINE, EMBASE, CINAHL, PsycINFO, BIOSIS Citation Index, Science Citation Index, ERIC, and Sociological Abstracts. We also searched the metaRegister of Controlled Trials, checked reference lists, and contacted study authors and other experts.
Two review authors assessed study eligibility independently. We included randomised controlled trials (RCT) and quasi-randomised controlled trials (quasi-RCT) that compared a PIP programme directed at parents with infants aged 24 months or less at study entry, with a control condition (i.e. waiting-list, no treatment or treatment-as-usual), and used at least one standardised measure of parental or infant functioning. We also included studies that only used a second treatment group.
We adhered to the standard methodological procedures of The Cochrane Collaboration. We standardised the treatment effect for each outcome in each study by dividing the mean difference (MD) in post-intervention scores between the intervention and control groups by the pooled standard deviation. We presented standardised mean differences (SMDs) and 95% confidence intervals (CI) for continuous data, and risk ratios (RR) for dichotomous data. We undertook meta-analysis using a random-effects model.
We included eight studies comprising 846 randomised participants, of which four studies involved comparisons of PIP with control groups only. Four studies involved comparisons with another treatment group (i.e. another PIP, video-interaction guidance, psychoeducation, counselling or cognitive behavioural therapy (CBT)), two of these studies included a control group in addition to an alternative treatment group. Samples included women with postpartum depression, anxious or insecure attachment, maltreated, and prison populations. We assessed potential bias (random sequence generation, allocation concealment, incomplete outcome data, selective reporting, blinding of participants and personnel, blinding of outcome assessment, and other bias). Four studies were at low risk of bias in four or more domains. Four studies were at high risk of bias for allocation concealment, and no study blinded participants or personnel to the intervention. Five studies did not provide adequate information for assessment of risk of bias in at least one domain (rated as unclear).Six studies contributed data to the PIP versus control comparisons producing 19 meta-analyses of outcomes measured at post-intervention or follow-up, or both, for the primary outcomes of parental depression (both dichotomous and continuous data); measures of parent-child interaction (i.e. maternal sensitivity, child involvement and parent engagement; infant attachment category (secure, avoidant, disorganised, resistant); attachment change (insecure to secure, stable secure, secure to insecure, stable insecure); infant behaviour and secondary outcomes (e.g. infant cognitive development). The results favoured neither PIP nor control for incidence of parental depression (RR 0.74, 95% CI 0.52 to 1.04, 3 studies, 278 participants, low quality evidence) or parent-reported levels of depression (SMD -0.22, 95% CI -0.46 to 0.02, 4 studies, 356 participants, low quality evidence). There were improvements favouring PIP in the proportion of infants securely attached at post-intervention (RR 8.93, 95% CI 1.25 to 63.70, 2 studies, 168 participants, very low quality evidence); a reduction in the number of infants with an avoidant attachment style at post-intervention (RR 0.48, 95% CI 0.24 to 0.95, 2 studies, 168 participants, low quality evidence); fewer infants with disorganised attachment at post-intervention (RR 0.32, 95% CI 0.17 to 0.58, 2 studies, 168 participants, low quality evidence); and an increase in the proportion of infants moving from insecure to secure attachment at post-intervention (RR 11.45, 95% CI 3.11 to 42.08, 2 studies, 168 participants, low quality evidence). There were no differences between PIP and control in any of the meta-analyses for the remaining primary outcomes (i.e. adverse effects), or secondary outcomes.Four studies contributed data at post-intervention or follow-up to the PIP versus alternative treatment analyses producing 15 meta-analyses measuring parent mental health (depression); parent-infant interaction (maternal sensitivity); infant attachment category (secure, avoidant, resistant, disorganised) and attachment change (insecure to secure, stable secure, secure to insecure, stable insecure); infant behaviour and infant cognitive development. None of the remaining meta-analyses of PIP versus alternative treatment for primary outcomes (i.e. adverse effects), or secondary outcomes showed differences in outcome or any adverse changes.We used the Grades of Recommendation, Assessment, Development and Evaluation Working Group (GRADE) approach to rate the overall quality of the evidence. For all comparisons, we rated the evidence as low or very low quality for parental depression and secure or disorganised infant attachment. Where we downgraded the evidence, it was because there was risk of bias in the study design or execution of the trial. The included studies also involved relatively few participants and wide CI values (imprecision), and, in some cases, we detected clinical and statistical heterogeneity (inconsistency). Lower quality evidence resulted in lower confidence in the estimate of effect for those outcomes.
AUTHORS' CONCLUSIONS: Although the findings of the current review suggest that PIP is a promising model in terms of improving infant attachment security in high-risk families, there were no significant differences compared with no treatment or treatment-as-usual for other parent-based or relationship-based outcomes, and no evidence that PIP is more effective than other methods of working with parents and infants. Further rigorous research is needed to establish the impact of PIP on potentially important mediating factors such as parental mental health, reflective functioning, and parent-infant interaction.
母婴心理治疗(PIP)是一种针对母婴双方的治疗方法,旨在改善母婴关系,促进婴儿依恋及最佳发育。PIP旨在通过关注母亲对婴儿的看法(这可能受其自身经历影响),并将其与母亲当前与孩子的关系联系起来,从而直接改善母婴关系。
我们于2014年1月13日检索了以下电子数据库:Cochrane对照试验中心注册库(CENTRAL,2014年第1期)、Ovid MEDLINE、EMBASE、CINAHL、PsycINFO、BIOSIS引文索引、科学引文索引、教育资源信息中心和社会学文摘。我们还检索了对照试验元注册库,检查了参考文献列表,并联系了研究作者及其他专家。
两位综述作者独立评估研究的纳入资格。我们纳入了随机对照试验(RCT)和半随机对照试验(quasi-RCT),这些试验比较了针对研究开始时年龄在24个月及以下婴儿的父母的PIP项目与对照条件(即等候名单、无治疗或常规治疗),并使用了至少一种父母或婴儿功能的标准化测量方法。我们还纳入了仅使用第二个治疗组的研究。
我们遵循Cochrane协作网的标准方法程序。我们通过将干预组和对照组干预后得分的平均差(MD)除以合并标准差,对每项研究中每个结果的治疗效果进行标准化。我们给出了连续数据的标准化平均差(SMD)和95%置信区间(CI),以及二分数据的风险比(RR)。我们使用随机效应模型进行荟萃分析。
我们纳入了八项研究,共846名随机参与者,其中四项研究仅涉及PIP与对照组的比较。四项研究涉及与另一个治疗组(即另一种PIP、视频互动指导、心理教育、咨询或认知行为疗法(CBT))的比较,其中两项研究除了替代治疗组外还包括一个对照组。样本包括产后抑郁、焦虑或不安全依恋、受虐待的女性以及监狱人群。我们评估了潜在偏倚(随机序列生成、分配隐藏、不完整的结果数据选择性报告、参与者和人员的盲法、结果评估的盲法以及其他偏倚)。四项研究在四个或更多领域的偏倚风险较低。四项研究在分配隐藏方面存在高偏倚风险,且没有研究对参与者或人员实施干预盲法。五项研究在至少一个领域未提供足够信息以评估偏倚风险(评为不清楚)。六项研究为PIP与对照的比较贡献了数据,针对父母抑郁的主要结果(二分数据和连续数据);亲子互动测量(即母亲敏感性、孩子参与度和父母投入度);婴儿依恋类别(安全型、回避型、混乱型、抵抗型);依恋变化(从不安全到安全、稳定安全、从安全到不安全、稳定不安全);婴儿行为和次要结果(如婴儿认知发展),在干预后或随访时或两者都进行了19项结果的荟萃分析。结果显示,在父母抑郁发生率(RR 0.74,95%CI 0.52至1.04,3项研究,278名参与者,低质量证据)或父母报告的抑郁水平方面(SMD -0.22,95%CI -0.46至0.02,4项研究,356名参与者,低质量证据),PIP和对照组均无优势。干预后,在安全依恋婴儿的比例方面有有利于PIP的改善(RR 8.93,95%CI 1.25至63.70,2项研究,168名参与者,极低质量证据);干预后回避型依恋风格婴儿的数量减少(RR 0.48,95%CI 0.24至0.95,2项研究,168名参与者,低质量证据);干预后混乱型依恋婴儿减少(RR 0.32,95%CI 0.17至0.58,2项研究,168名参与者,低质量证据);干预后从不安全依恋转变为安全依恋的婴儿比例增加(RR 11.45,95%CI 3.11至42.08,2项研究,168名参与者,低质量证据)。在其余主要结果(即不良反应)或次要结果的任何荟萃分析中,PIP与对照组之间均无差异。四项研究为PIP与替代治疗分析贡献了干预后或随访时的数据,进行了15项荟萃分析,测量父母心理健康(抑郁);亲子互动(母亲敏感性);婴儿依恋类别(安全型、回避型、抵抗型、混乱型)和依恋变化(从不安全到安全、稳定安全、从安全到不安全、稳定不安全);婴儿行为和婴儿认知发展。在其余PIP与替代治疗的主要结果(即不良反应)或次要结果的荟萃分析中,均未显示出结果差异或任何不良变化。我们使用推荐分级、评估、制定与评价工作组(GRADE)方法对证据的总体质量进行评级。对于所有比较,我们将父母抑郁和安全或混乱的婴儿依恋的证据评级为低或极低质量。当我们降低证据等级时,是因为研究设计或试验执行中存在偏倚风险。纳入的研究参与者相对较少,置信区间较宽(不精确),并且在某些情况下,我们检测到临床和统计异质性(不一致)。较低质量的证据导致对这些结果效应估计的信心降低。
尽管当前综述的结果表明,在改善高危家庭婴儿依恋安全性方面,PIP是一个有前景的模式,但与无治疗或常规治疗相比,在其他基于父母或基于关系的结果方面没有显著差异,并且没有证据表明PIP比其他与父母和婴儿合作的方法更有效。需要进一步进行严格研究,以确定PIP对父母心理健康、反思功能和亲子互动等潜在重要中介因素的影响。