Fruchart M F, Rolland E, Courtois F, Meier F, Besse-Moreau M, Foucher E, Engelmann P
Service de Gynéco-Obstétrique, Hôpital Louis-Mourier, Colombes.
J Gynecol Obstet Biol Reprod (Paris). 1995;24(2):204-8.
Evaluation (usefulness and safety) of programmed autologous transfusion in obstetrics. SITE. Blood Transfusion Centre, Hôpital Louis-Mourier, F 92700 Colombes.
Prospective study of 150 patients for whom blood withdrawal was planned during the last month of pregnancy. Entry criteria were either a risk of haemorrhage or persistent patient request.
Two withdrawals were planned during the last month of pregnancy at the out-patient clinic at a one-week interval. The autologous units were transfused per-partum in case of haemorrhage and/or post-partum in case of anaemia.
One hundred pregnant women entered the protocol (43 had a risk of haemorrhage). Both preplanned withdrawals were made in 60 of these patients. Per-partum transfusions were necessary in only 7 patients including 4/43 with a risk factor (9%) and 3/57 with no risk factor (5%). Post-partum transfusions were made in 22 other patients. Consequently, 117 of the 160 units collected were not used (73%).
Despite good tolerance (5% incidence) due to the known problems in evaluating the risk of haemorrhage and the small percentage of patients without risk factors who were transfused per-partum, we have decided to reserve this protocol for patients with an authentically identified risk of haemorrhage (placenta praevia, cesarean section, uterine scar tissue).
评估产科计划性自体输血的效果(有效性和安全性)。地点:法国92700科隆布市路易 - 穆里耶医院输血中心。
对150名计划在妊娠最后一个月进行采血的患者进行前瞻性研究。纳入标准为有出血风险或患者持续要求。
计划在妊娠最后一个月于门诊进行两次采血,间隔一周。自体血单位在出血时用于分娩期输血,或在贫血时用于产后输血。
100名孕妇纳入该方案(43名有出血风险)。其中60名患者完成了两次计划采血。仅7名患者需要分娩期输血,包括4/43有风险因素者(9%)和3/57无风险因素者(5%)。另有22名患者进行了产后输血。因此,采集的160个单位血液中有117个未使用(73%)。
尽管耐受性良好(发生率5%),但由于评估出血风险存在已知问题,且分娩期接受输血的无风险因素患者比例较小,我们决定将该方案保留给真正确定有出血风险的患者(前置胎盘、剖宫产、子宫瘢痕组织)。