Rozenberg P
Département d'obstétrique et gynécologie, EA 7285, hôpital Poissy-Saint-Germain, université Versailles-St Quentin, France.
J Gynecol Obstet Biol Reprod (Paris). 2016 Dec;45(10):1337-1345. doi: 10.1016/j.jgyn.2016.09.023. Epub 2016 Oct 28.
The ultrasonographic measurement of cervical length with a cutoff of 15mm is currently the best method to identify a group of asymptomatic women in the general population at risk of spontaneous preterm birth, especially among asymptomatic patients with a singleton pregnancy with no history of preterm birth. Cerclage and 17 alpha-hydroxyprogesterone caproate (17OHP-C) are ineffective to reduce the risk of preterm birth among asymptomatic patients with a short cervix in midtrimester. However, vaginal progesterone (200-mg capsules of micronized progesterone or gel containing 90mg progesterone) has been demonstrated effective in 2 large randomized trials to reduce the risk of preterm birth and possibly the composite morbidity and perinatal mortality associated among asymptomatic women with a short cervix in the general population screened by ultrasound of the cervix in midtrimester. Three cost-effectiveness analyses are converging to show that universal screening for cervical length with vaginal progesterone treatment seems to be cost-effective compared with no screening. However, it is too early to definitively conclude that universal screening is justified for several reasons: many women must be screened to prevent a relatively small number of preterm births. Moreover, the epidemiology of preterm delivery is such that the use of progesterone in asymptomatic women with a short cervix screened by ultrasound in midtrimester in the general population will not significantly reduce the prevalence of preterm births; there are no data comparing the effectiveness of universal ultrasound screening followed by vaginal progesterone treatment in case of short cervix versus no universal screening associated to a progesterone treatment in case of incidentally observed short cervix; the universal ultrasound screening may not produce the same results in practice than those observed in published randomized trials, due to population differences, "indication creep", or "stretching of the cutoff" defining the short cervix. Moreover, the implementation of unevaluated or not recommended treatments, such as bed rest, tocolytics, 17OHP-C or cerclage, can potentially cause unintended deleterious consequences and reduce the cost-effectiveness; the cost-effectiveness analyses evaluating universal screening for cervical length present uncertainties on critical variables, notably the short cervix prevalence and the progesterone efficacy. In conclusion, although the implementation of such a screening strategy can be considered by individual practitioners, this screening cannot be universally mandated.
目前,超声测量宫颈长度并以15毫米为临界值,是在普通人群中识别出有自发早产风险的无症状女性群体的最佳方法,尤其是在无早产史的单胎妊娠无症状患者中。对于孕中期宫颈短的无症状患者,宫颈环扎术和己酸17α - 羟孕酮(17OHP - C)在降低早产风险方面无效。然而,阴道用黄体酮(200毫克微粉化黄体酮胶囊或含90毫克黄体酮的凝胶)已在两项大型随机试验中被证明可有效降低早产风险,并可能降低普通人群中经孕中期宫颈超声筛查出的宫颈短的无症状女性的综合发病率和围产期死亡率。三项成本效益分析趋于表明,与不进行筛查相比,对宫颈长度进行普遍筛查并给予阴道用黄体酮治疗似乎具有成本效益。然而,由于以下几个原因,现在就下结论说普遍筛查是合理的还为时过早:必须对许多女性进行筛查才能预防相对少数的早产。此外,早产的流行病学情况使得在普通人群中对孕中期经超声筛查出宫颈短的无症状女性使用黄体酮,并不会显著降低早产的发生率;没有数据比较在宫颈短的情况下进行普遍超声筛查并随后给予阴道用黄体酮治疗与在偶然发现宫颈短时不进行普遍筛查但给予黄体酮治疗的效果;由于人群差异、“指征扩展”或定义宫颈短的“临界值放宽”,普遍超声筛查在实际应用中可能不会产生与已发表的随机试验中观察到的相同结果。此外,实施未经评估或不推荐的治疗方法,如卧床休息、宫缩抑制剂、17OHP - C或宫颈环扎术,可能会潜在地导致意外的有害后果并降低成本效益;评估宫颈长度普遍筛查的成本效益分析在关键变量上存在不确定性,特别是宫颈短的患病率和黄体酮的疗效。总之,虽然个体从业者可以考虑实施这种筛查策略,但不能普遍强制进行这种筛查。