Brennan Miriam, Young Gavin, Devane Declan
School of Nursing and Midwifery, National University of Ireland Galway, Galway, Ireland.
Cochrane Database Syst Rev. 2012 Nov 14;11(11):CD000066. doi: 10.1002/14651858.CD000066.pub2.
Striae gravidarum (stretch marks developing during pregnancy) occur in 50% to 90% of women. They appear as red or purple lines or streaks that fade slowly to leave pale lines or marks on the skin. The abdomen, breasts and thighs are commonly affected. The exact cause of stretch marks is unclear and no preparation has yet been shown to be effective in preventing the development of stretch marks. They are a source of significant anxiety for women, impacting on their quality of life.
To assess the effects of topical preparations on the prevention of stretch marks in pregnancy.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (31 October 2011) and reference lists of retrieved reports.
We included randomised controlled trials and quasi-randomised controlled trials comparing topical preparations (with active ingredients) with other topical preparations (with active ingredients), with a placebo (that is, preparations without active ingredients) or with no treatment for the prevention of stretch marks in pregnant women.
Three review authors independently assessed trial eligibility and trial quality, and extracted data. Data were checked for accuracy. The primary outcome was the presence of stretch marks and the secondary outcome was the severity of stretch marks.
We included six trials involving 800 women. Of the six trials, we judged the risk of bias for three as 'low risk' for random sequence generation, blinding of participants and personnel, blinding of outcome assessment, completeness of outcome data and selective reporting.There was no statistically significant average difference in the development of stretch marks in women who received topical preparations with active ingredients compared to women who received a placebo or no treatment (average risk ratio (RR) 0.74; 95% confidence interval (CI) 0.53 to 1.03; five trials, 474 women; random-effects model, Tau² = 0.09, I² = 65%) (Analysis 1.1).Results were consistent with the main effects when we performed a sensitivity analysis excluding studies judged to be at high risk of bias for random sequence generation, allocation concealment or more than 20% missing data for a given outcome (average RR 0.81; 95% CI 0.60 to 1.10; four trials, 424 women; random-effects model, Tau² = 0.05, I² = 57%).The was no statistically significant average mean difference in the severity of stretch marks (standardised mean difference (SMD) -0.31; 95% CI -1.06 to 0.44; two trials, 255 women; Tau² = 0.26, I² = 87%).There was no statistically significant difference in the development of stretch marks in women who received topical preparations with active ingredients compared to women who received other topical preparations with active ingredients (average RR 0.51; 95% CI 0.16 to 1.60; two trials, 305 women; Tau² = 0.53, I² = 74%). There was no statistically significant difference in the severity of stretch marks (mean difference (MD) -0.20; 95% CI -0.53 to 0.13; one trial, 206 women; heterogeneity not applicable).
AUTHORS' CONCLUSIONS: We found no high-quality evidence to support the use of any of the topical preparations in the prevention of stretch marks during pregnancy. There is a clear need for robust, methodologically rigorous randomised trials involving larger sample sizes to evaluate the effects of topical preparations on the development of stretch marks in pregnancy. In addition, it is important that preparations commonly used by women to prevent and treat stretch marks are evaluated within the context of robust, methodologically rigorous and adequately powered randomised trials.
妊娠纹(孕期出现的妊娠纹)在50%至90%的女性中出现。它们表现为红色或紫色的线条或条纹,会慢慢褪色,在皮肤上留下浅色的线条或痕迹。腹部、乳房和大腿是常见的受累部位。妊娠纹的确切病因尚不清楚,目前尚无任何制剂被证明能有效预防妊娠纹的形成。它们是女性严重焦虑的来源,影响着她们的生活质量。
评估局部制剂对预防孕期妊娠纹的效果。
我们检索了Cochrane妊娠与分娩组试验注册库(2011年10月31日)以及检索报告的参考文献列表。
我们纳入了随机对照试验和半随机对照试验,这些试验比较了含活性成分的局部制剂与其他含活性成分的局部制剂、安慰剂(即不含活性成分的制剂)或不进行治疗对预防孕妇妊娠纹的效果。
三位综述作者独立评估试验的合格性和试验质量,并提取数据。对数据进行准确性检查。主要结局是妊娠纹的出现情况,次要结局是妊娠纹的严重程度。
我们纳入了6项涉及800名女性的试验。在这6项试验中,我们判定3项试验在随机序列生成、参与者和人员的盲法、结局评估的盲法、结局数据的完整性以及选择性报告方面的偏倚风险为“低风险”。与接受安慰剂或不进行治疗的女性相比,接受含活性成分局部制剂的女性在妊娠纹形成方面没有统计学上的显著平均差异(平均风险比(RR)0.74;95%置信区间(CI)0.53至1.03;5项试验,474名女性;随机效应模型,Tau² = 0.09,I² = 65%)(分析1.1)。当我们进行敏感性分析,排除在随机序列生成、分配隐藏或给定结局缺失数据超过20%方面被判定为高偏倚风险的研究时,结果与主要效应一致(平均RR 0.81;95% CI 0.60至1.10;4项试验,424名女性;随机效应模型,Tau² = 0.05,I² = 57%)。妊娠纹严重程度方面没有统计学上的显著平均差异(标准化平均差(SMD)-0.31;95% CI -1.06至0.44;2项试验,255名女性;Tau² = 0.26,I² = 87%)。与接受其他含活性成分局部制剂的女性相比,接受含活性成分局部制剂的女性在妊娠纹形成方面没有统计学上的显著差异(平均RR 0.51;95% CI 0.16至1.60;2项试验,305名女性;Tau² = 0.53,I² = 74%)。妊娠纹严重程度方面没有统计学上的显著差异(平均差(MD)-0.20;95% CI -