CASE REPORTTransfusion practice in major obstetric haemorrhage: lessons from trauma
Introduction
Major obstetric haemorrhage is defined as a blood loss of 2500 mL or more, transfusion of five units of red blood cells or treatment of a coagulopathy.1, 2 Obstetric resuscitation often starts with administration of clear intravenous fluids and packed red blood cells (pRBC), following which the use of clotting products and platelets is considered, often guided by coagulation studies that delay treatment.3 The UK National Patient Safety Agency (NPSA) recommends monitoring laboratory blood tests during massive transfusion, but also that administration of blood and blood products should not be delayed while awaiting results.1, 3, 4, 5
Resuscitation of bleeding patients with crystalloid, colloid and plasma-poor pRBC at the same time that clotting factors are being consumed results in the concentration of plasma coagulation factors falling to <40%, and typically occurs before 10 units of pRBC have been given.6 Disseminated intravascular coagulopathy in obstetric haemorrhage can also occur early, especially if haemorrhage is not treated rapidly. Early treatment of massive haemorrhage after trauma using fresh frozen plasma (FFP) and pRBC in a 1:1 ratio, current practice in US and British military, is thought to improve survival.6, 7, 8, 9, 10, 11 Military guidelines for haemorrhagic shock also recommend administration of platelets in a 1:1 ratio with pRBC.7, 8, 9, 11
Prevention of coagulopathy should be better than its treatment and requires anticipation.6 Some authors advise that replacement of clotting factors should be made on clinical grounds, rather than based on laboratory results.4, 7, 11, 12 The Association of Anaesthetists of Great Britain and Ireland (AAGBI) guideline recommends early infusion of FFP (15 mL/kg) to prevent haemostatic failure and may need to be started if a senior clinician anticipates massive haemorrhage.13 This guideline emphasises the importance of preventing haemostatic failure because, once established, standard regimens of FFP infusion are likely to be inadequate and larger volumes will be required with greater risk to the patient and cost implications for the hospital.13
For massive obstetric haemorrhage, a ratio of 6:4:1 for pRBC:FFP:platelets has been suggested. If bleeding continues after initial treatment, consideration should be given to increasing the amount of FFP to give a ratio of 4:4:1.5 Point-of-care tests can measure haemoglobin concentration and the coagulation profile, and may guide blood product replacement following initial resuscitation. Three cases of major obstetric haemorrhage treated using these principles are described. In each case the patients’ blood results (Table 1, Table 2, Table 3) and fluid replacement (Table 4) are listed.
Section snippets
Case 1
A 26-year-old, healthy, nulliparous woman was scheduled for elective caesarean delivery at term due to a transverse fetal position. Her pre-operative haemoglobin (Hb) was 11.7 g/dL. Monitoring of non-invasive blood pressure (BP), electrocardiogram (ECG) and oxygen saturation were started. Compound sodium lactate 1000 mL was infused and spinal anaesthesia with hyperbaric bupivacaine 12.5 mg and diamorphine 500 μg at the L3-4 interspace produced surgical anaesthesia to T4. A phenylephrine infusion (1
Case 2
A 37-year-old healthy woman presented for elective caesarean delivery at 36 weeks of gestation with an anterior grade-4 placenta praevia. She had undergone two previous caesarean deliveries. Two 14-gauge intravenous cannulae and an epidural catheter were inserted. In the radiology department bilateral intravascular balloon catheters were placed in the anterior branches of the internal iliac arteries. In the operating room (OR), epidural anaesthesia using 17 mL of a mixture containing equal
Case 3
A 26-year-old woman, in her second pregnancy at term, had a prolonged labour with a normal vaginal delivery, but sustained perineal tears. During the repair she became haemodynamically unstable. Fluid resuscitation started with Gelofusine 1000 mL and crystalloid 1500 mL. Hemocue showed a Hb concentration of 5.4 g/dL and 2 units O-Rh negative, uncrossmatched blood were given during transfer to the OR. General anaesthesia was induced with a modified rapid sequence technique using ketamine and
Discussion
Transfusion of blood and blood products in trauma and major haemorrhage is changing as a result of experience in military medicine. Current trauma practice advises early use of pRBC, platelets and clotting products in high ratios. Resuscitation in obstetric haemorrhage is similar to that in trauma as both aim to stop bleeding, maintain efficient oxygen delivery and prevent development of the “lethal triad” of acidosis, coagulopathy and hypothermia.3, 5, 14, 15 However, in the obstetric patient
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Thromboelastometry-guided treatment algorithm in postpartum haemorrhage: a randomised, controlled pilot trial
2023, British Journal of AnaesthesiaPost-partum transfusion: The view of the anaesthetist in a delivery room
2019, Transfusion Clinique et BiologiqueManagement of postpartum haemorrhage: from research into practice, a narrative review of the literature and the Cardiff experience
2019, International Journal of Obstetric AnesthesiaCitation Excerpt :Median (IQR) blood loss was 1500 mL (1300–2000 mL) and none of the women developed haemostatic impairment,21 suggesting that haemostatic impairment during PPH can be assessed accurately using VE-POCTs. It has been suggested that a massive transfusion protocol used for PPH should include platelets.18,20,45,46 Guidelines recommend maintaining the platelet count above 75 × 109/L during PPH.8,9
Viscoelastometry guided fresh frozen plasma infusion for postpartum haemorrhage: OBS2, an observational study
2017, British Journal of AnaesthesiaCitation Excerpt :Restrictive use of FFP, guided by Fibtem, is not standard practice and many guidelines recommend empirical, fixed-ratio FFP if laboratory results are not available.2 4 8 The challenge facing clinicians treating PPH is that they do not have timely tests of coagulation and, to treat the minority of women with haemostatic compromise, women with normal haemostasis must also be treated.6 7 9–11 At present NICE does not support the use of VE-POCTs during PPH, but recommends studies investigating the clinical and cost effectiveness of this technology.
Managing major obstetric haemorrhage: Pharmacotherapy and transfusion
2017, Best Practice and Research: Clinical AnaesthesiologyCitation Excerpt :The risk factors for requiring a platelet transfusion were blood loss >4500 mL, placenta abruption and pre-delivery thrombocytopenia due to idiopathic thrombocytopenia purpura, preeclampsia or gestational thrombocytopenia [77]. Protocols that recommend a 1:1:1 RBC:plasma:platelet transfusion ratio [50] will likely result in multiple platelet transfusions well above recommended levels and on current evidence, empiric transfusion cannot be justified. There has been a large increase in interest around factor concentrate use during all types of major haemorrhages.
Obstetric Hemorrhage: Prevention, Recognition, and Treatment
2017, Advances in AnesthesiaCitation Excerpt :PLT transfusion during PPH is somewhat controversial. Some investigators argue that PLT should be transfused early in a fixed ratio to RBC and FFP, similar to trauma patients [65,93]. However, PPH-related coagulopathy patterns remain distinct from those of trauma patients, and the literature remains scarce on the best evidence-based strategy for PLT transfusion during PPH.