Am J Obstet Gynecol. 2023 Sep;229(3):B2-B19. doi: 10.1016/j.ajog.2023.05.019. Epub 2023 May 24.
Maternal sepsis is a significant cause of maternal morbidity and mortality, and is a potentially preventable cause of maternal death. This Consult aims to summarize what is known about sepsis and provide guidance for the management of sepsis during pregnancy and the postpartum period. Most studies cited are from the nonpregnant population, but where available, pregnancy data are included. The following are the Society for Maternal-Fetal Medicine recommendations: (1) we recommend that clinicians consider the diagnosis of sepsis in pregnant or postpartum patients with otherwise unexplained end-organ damage in the presence of a suspected or confirmed infectious process, regardless of the presence of fever (GRADE 1C); (2) we recommend that sepsis and septic shock in pregnancy be considered medical emergencies and that treatment and resuscitation begin immediately (Best Practice); (3) we recommend that hospitals and health systems use a performance improvement program for sepsis in pregnancy with sepsis screening tools and metrics (GRADE 1B); (4) we recommend that institutions develop their own procedures and protocols for the detection of maternal sepsis, avoiding the use of a single screening tool alone (GRADE 1B); (5) we recommend obtaining tests to evaluate for infectious and noninfectious causes of life-threatening organ dysfunction in pregnant and postpartum patients with possible sepsis (Best Practice); (6) we recommend that an evaluation for infectious causes in pregnant or postpartum patients in whom sepsis is suspected or identified includes appropriate microbiologic cultures, including blood, before starting antimicrobial therapy, as long as there are no substantial delays in timely administration of antibiotics (Best Practice); (7) we recommend obtaining a serum lactate level in pregnant or postpartum patients in whom sepsis is suspected or identified (GRADE 1B); (8) in pregnant or postpartum patients with septic shock or a high likelihood of sepsis, we recommend administration of empiric broad-spectrum antimicrobial therapy, ideally within 1 hour of recognition (GRADE 1C); (9) after a diagnosis of sepsis in pregnancy is made, we recommend rapid identification or exclusion of an anatomic source of infection and emergency source control when indicated (Best Practice); (10) we recommend early intravenous administration (within the first 3 hours) of 1 to 2 L of balanced crystalloid solutions in sepsis complicated by hypotension or suspected organ hypoperfusion (GRADE 1C); (11) we recommend the use of a balanced crystalloid solution as a first-line fluid for resuscitation in pregnant and postpartum patients with sepsis or septic shock (GRADE 1B); (12) we recommend against the use of starches or gelatin for resuscitation in pregnant and postpartum patients with sepsis or septic shock (GRADE 1A); (13) we recommend ongoing, detailed evaluation of the patient's response to fluid resuscitation guided by dynamic measures of preload (GRADE 1B); (14) we recommend the use of norepinephrine as the first-line vasopressor during pregnancy and the postpartum period with septic shock (GRADE 1C); (15) we suggest using intravenous corticosteroids in pregnant or postpartum patients with septic shock who continue to require vasopressor therapy (GRADE 2B); (16) because of an increased risk of venous thromboembolism in sepsis and septic shock, we recommend the use of pharmacologic venous thromboembolism prophylaxis in pregnant and postpartum patients in septic shock (GRADE 1B); (17) we suggest initiating insulin therapy at a glucose level >180 mg/dL in critically ill pregnant patients with sepsis (GRADE 2C); (18) if a uterine source for sepsis is suspected or confirmed, we recommend prompt delivery or evacuation of uterine contents to achieve source control, regardless of gestational age (GRADE 1C); and (19) because of an increased risk of physical, cognitive, and emotional problems in survivors of sepsis and septic shock, we recommend ongoing comprehensive support for pregnant and postpartum sepsis survivors and their families (Best Practice).
产妇脓毒症是产妇发病率和死亡率的一个重要原因,也是孕产妇死亡的一个潜在可预防原因。本次咨询旨在总结关于脓毒症的知识,并为妊娠和产后期间脓毒症的管理提供指导。大多数引用的研究来自非孕妇人群,但在有可用数据的情况下,也包括了妊娠数据。现将母胎医学学会的建议总结如下:(1)我们建议临床医生在疑似或确诊感染过程中,出现不明原因的终末器官损伤的妊娠或产后患者中考虑脓毒症的诊断,无论是否存在发热(GRADE 1C);(2)我们建议将妊娠脓毒症和脓毒性休克视为医疗紧急情况,应立即开始治疗和复苏(最佳实践);(3)我们建议医院和卫生系统使用妊娠脓毒症的绩效改进计划,包括脓毒症筛查工具和指标(GRADE 1B);(4)我们建议各机构制定自己的检测程序和方案,以避免单独使用单一筛查工具来检测产妇脓毒症(GRADE 1B);(5)我们建议对疑似或确诊为脓毒症的妊娠和产后患者进行危及生命的器官功能障碍的感染和非感染原因的检测(最佳实践);(6)我们建议对疑似或确诊为脓毒症的妊娠或产后患者,在开始使用抗生素之前,应进行适当的微生物学培养,包括血培养,只要抗生素的及时使用没有实质性延迟(最佳实践);(7)我们建议对疑似或确诊为脓毒症的妊娠或产后患者检测血清乳酸水平(GRADE 1B);(8)对于脓毒性休克或高度怀疑脓毒症的妊娠或产后患者,我们建议在 1 小时内开始使用经验性广谱抗菌治疗(GRADE 1C);(9)一旦确诊为妊娠脓毒症,我们建议迅速确定或排除感染的解剖源,并在需要时进行紧急源控制(最佳实践);(10)我们建议在伴有低血压或疑似器官低灌注的脓毒症复杂化患者中,在 3 小时内快速静脉给予 1 至 2 L 平衡晶体溶液(GRADE 1C);(11)我们建议在妊娠和产后脓毒症或脓毒性休克患者中使用平衡晶体溶液作为复苏的一线液体(GRADE 1B);(12)我们建议在妊娠和产后脓毒症或脓毒性休克患者中不使用淀粉或明胶进行复苏(GRADE 1A);(13)我们建议在妊娠和产后脓毒症或脓毒性休克患者中,根据对前负荷的动态评估指导液体复苏(GRADE 1B);(14)我们建议在脓毒性休克期间使用去甲肾上腺素作为妊娠和产后的一线血管加压药(GRADE 1C);(15)我们建议对继续需要血管加压治疗的脓毒性休克妊娠或产后患者使用静脉皮质类固醇(GRADE 2B);(16)由于脓毒症和脓毒性休克患者静脉血栓栓塞风险增加,我们建议对脓毒性休克的妊娠和产后患者使用药物预防静脉血栓栓塞(GRADE 1B);(17)我们建议在患有脓毒症的危重孕妇中,血糖水平>180 mg/dL 时开始胰岛素治疗(GRADE 2C);(18)如果怀疑或确诊为子宫来源的脓毒症,我们建议迅速分娩或排空子宫内容物以实现源控制,无论胎龄如何(GRADE 1C);(19)由于脓毒症和脓毒性休克幸存者可能存在身体、认知和情感问题,我们建议对妊娠和产后脓毒症幸存者及其家属提供持续的全面支持(最佳实践)。