Dodd J, Dare M R, Middleton P
Department of Obstetrics and Gynaecology, University of Adelaide, Women's and Children's Hospital, 72 King William Road, Adelaide, South Australia, Australia, 5006.
Cochrane Database Syst Rev. 2004 Oct 18;2004(4):CD004222. doi: 10.1002/14651858.CD004222.pub2.
Postpartum anaemia is associated with breathlessness, tiredness, palpitations and maternal infections. Blood transfusions or iron supplementation have been used in the treatment of iron deficiency anaemia. Recently other anaemia treatments, in particular erythropoietin therapy, have also been used.
To assess the clinical effects of treatments for postpartum anaemia, including oral, intravenous or subcutaneous iron/folate supplementation and erythropoietin administration, and blood transfusion.
We searched the Cochrane Pregnancy and Childbirth Group trials register (30 May 2004), the Cochrane Central Register of Controlled Trials (The Cochrane Library, Issue 1, 2003), MEDLINE (1966 to March 2003), EMBASE (1980 to March 2003), Current Contents and ACP Journal Club (from inception to March 2003).
Randomised controlled trials (RCTs) comparing therapy for postpartum iron deficiency anaemia (oral, intravenous or subcutaneous administration of iron, folate, erythropoietin or blood transfusion) with placebo, another treatment or no treatment.
Two reviewers independently assessed trial quality and extracted data.
Six included RCTs involving 411 women described treatment with erythropoietin or iron as their primary interventions. No RCTs were identified that assessed treatment with blood transfusion. Few outcomes relating to clinical maternal and neonatal factors were reported: studies focused largely on surrogate outcomes such as haematological indices. Overall, the methodological quality of the included RCTs was reasonable; however, their usefulness in this review is restricted by the interventions and outcomes reported. When compared with iron therapy only, erythropoietin increased the likelihood of lactation at discharge from hospital (1 RCT, n = 40; relative risk (RR) 1.90, 95% confidence interval (CI) 1.21 to 2.98). No apparent effect on need for blood transfusions was found, when erythropoietin plus iron was compared to treatment with iron only (2 RCTs, n = 100; RR 0.20, 95% CI 0.01 to 3.92), although the RCTs may have been of insufficient size to rule out important clinical differences. Haematological indices (haemoglobin and haemocrit) showed some increases when erythropoietin was compared to iron only, iron and folate, but not when compared with placebo.
REVIEWERS' CONCLUSIONS: There is some limited evidence of favourable outcomes for treatment of postpartum anaemia with erythropoietin. However, most of the available literature focuses on laboratory haematological indices, rather than clinical outcomes. Further high-quality trials assessing the treatment of postpartum anaemia with iron supplementation and blood transfusions are required. Future trials may also examine the significance of the severity of anaemia in relation to treatment, and an iron-rich diet as an intervention.
产后贫血与呼吸急促、疲劳、心悸及产妇感染有关。输血或补充铁剂已用于治疗缺铁性贫血。近来,其他贫血治疗方法,尤其是促红细胞生成素疗法也已被采用。
评估产后贫血治疗方法的临床效果,包括口服、静脉或皮下补充铁/叶酸、给予促红细胞生成素及输血。
我们检索了Cochrane妊娠与分娩组试验注册库(2004年5月30日)、Cochrane对照试验中央注册库(《Cochrane图书馆》,2003年第1期)、MEDLINE(1966年至2003年3月)、EMBASE(1980年至2003年3月)、《现刊目次》及《美国内科医师学会杂志俱乐部》(创刊至2003年3月)。
比较产后缺铁性贫血治疗方法(口服、静脉或皮下给予铁剂、叶酸、促红细胞生成素或输血)与安慰剂、另一种治疗方法或不治疗的随机对照试验(RCT)。
两名评价员独立评估试验质量并提取数据。
6项纳入的RCT涉及411名妇女,将促红细胞生成素或铁剂治疗作为主要干预措施。未发现评估输血治疗的RCT。关于产妇和新生儿临床因素的结局报道较少:研究主要集中于替代结局,如血液学指标。总体而言,纳入的RCT的方法学质量合理;然而,其在本综述中的有用性受到所报道的干预措施和结局的限制。与仅用铁剂治疗相比,促红细胞生成素增加了出院时泌乳的可能性(1项RCT,n = 40;相对危险度(RR)1.90,95%置信区间(CI)1.21至2.98)。当促红细胞生成素加铁剂与仅用铁剂治疗比较时,未发现对输血需求有明显影响(2项RCT,n = 100;RR 0.20,95% CI 0.01至3.92),尽管这些RCT的样本量可能不足以排除重要的临床差异。与仅用铁剂、铁剂加叶酸相比,促红细胞生成素治疗后血液学指标(血红蛋白和血细胞比容)有所升高,但与安慰剂相比则未升高。
有一些有限的证据表明促红细胞生成素治疗产后贫血有良好结局。然而,大多数现有文献关注的是实验室血液学指标,而非临床结局。需要进一步进行高质量试验以评估补充铁剂和输血治疗产后贫血的效果。未来的试验还可研究贫血严重程度与治疗的关系以及富含铁饮食作为一种干预措施的意义。