Gillon Tessa E R, Pels Anouk, von Dadelszen Peter, MacDonell Karen, Magee Laura A
VU medical centre, Amsterdam, the Netherlands.
Academic Medical Center, Amsterdam, The Netherlands.
PLoS One. 2014 Dec 1;9(12):e113715. doi: 10.1371/journal.pone.0113715. eCollection 2014.
Clinical practice guidelines (CPGs) are developed to assist health care providers in decision-making. We systematically reviewed existing CPGs on the HDPs (hypertensive disorders of pregnancy) to inform clinical practice.
METHODOLOGY & PRINCIPAL FINDINGS: MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials, Cochrane Methodology Register, Health Technology Assessments, and Database of Abstracts of Reviews of Effects (Ovid interface), Grey Matters, Google Scholar, and personal records were searched for CPGs on the HDPs (Jan/03 to Nov/13) in English, French, Dutch, or German. Of 13 CPGs identified, three were multinational and three developed for community/midwifery use. Length varied from 3-1188 pages and three guidelines did not formulate recommendations. Eight different grading systems were identified for assessing evidence quality and recommendation strength. No guideline scored ≧80% on every domain of the AGREE II, a tool for assessing guideline methodological quality; two CPGs did so for 5/6 domains. Consistency was seen for (i) definitions of hypertension, proteinuria, chronic and gestational hypertension; (ii) pre-eclampsia prevention for women at increased risk: calcium when intake is low and low-dose aspirin, but not vitamins C and E or diuretics; (iii) antihypertensive treatment of severe hypertension; (iv) MgSO4 for eclampsia and severe pre-eclampsia; (v) antenatal corticosteroids at <34 wks when delivery is probable within 7 days; (vi) delivery for women with severe pre-eclampsia pre-viability or pre-eclampsia at term; and (vii) active management of the third stage of labour with oxytocin. Notable inconsistencies were in: (i) definitions of pre-eclampsia and severe pre-eclampsia; (ii) target BP for non-severe hypertension; (iii) timing of delivery for women with pre-eclampsia and severe pre-eclampsia; (iv) MgSO4 for non-severe pre-eclampsia, and (v) postpartum maternal monitoring.
Existing international HDP CPGs have areas of consistency with which clinicians and researchers can work to develop auditable standards, and areas of inconsistency that should be addressed by future research.
制定临床实践指南(CPG)旨在帮助医疗服务提供者进行决策。我们系统回顾了现有的关于妊娠高血压疾病(HDP)的CPG,以为临床实践提供参考。
检索了MEDLINE、EMBASE、Cochrane对照试验中心注册库、Cochrane方法学注册库、卫生技术评估数据库以及循证医学数据库(Ovid界面)、Grey Matters、谷歌学术和个人记录,查找2003年1月至2013年11月期间以英文、法文、荷兰文或德文发表的关于HDP的CPG。在检索到的13篇CPG中,3篇为跨国指南,3篇是为社区/助产使用而制定的。篇幅从3页到1188页不等,3篇指南未给出推荐意见。确定了8种不同的分级系统用于评估证据质量和推荐强度。在用于评估指南方法学质量的AGREE II工具的每个领域,没有一篇指南得分≥80%;有2篇CPG在6个领域中的5个领域达到了这一标准。在以下方面存在一致性:(i)高血压、蛋白尿、慢性高血压和妊娠期高血压的定义;(ii)对高危女性预防子痫前期:钙摄入量低时补充钙剂和小剂量阿司匹林,但不包括维生素C、维生素E或利尿剂;(iii)重度高血压的降压治疗;(iv)硫酸镁用于子痫和重度子痫前期;(v)孕34周前、预计7天内可能分娩时使用产前糖皮质激素;(vi)重度子痫前期未足月或足月子痫前期女性的分娩;(vii)使用缩宫素积极处理第三产程。显著的不一致之处在于:(i)子痫前期和重度子痫前期的定义;(ii)非重度高血压的血压控制目标;(iii)子痫前期和重度子痫前期女性的分娩时机;(iv)硫酸镁用于非重度子痫前期;(v)产后产妇监测。
现有的国际HDP CPG有一些一致的方面,临床医生和研究人员可据此制定可审计的标准,也有一些不一致的方面有待未来研究解决。