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2019年脓毒症护理路径

Sepsis Care Pathway 2019.

作者信息

Labib Ahmed

机构信息

Medical Intensive Care Unit, Hamad General Hospital, Hamad Medical Corporation, Doha, Qatar.

出版信息

Qatar Med J. 2019 Nov 7;2019(2):4. doi: 10.5339/qmj.2019.qccc.4. eCollection 2019.

Abstract

Sepsis, a medical emergency and life-threatening disorder, results from abnormal host response to infection that leads to acute organ dysfunction. Sepsis is a major killer across all ages and countries and remains the most common cause of admission and death in the Intensive Care Unit (ICU). The true incidence remains elusive and estimates of the global burden of sepsis remain a wild guess. One study suggested over 19 million cases and 5 million sepsis-related deaths annually. Addressing the challenge, the World Health Assembly of the World Health Organisation (WHO) passed a resolution on better prevention, diagnosis, and management of sepsis. Despite thousands of articles and hundreds of trials, sepsis remains a major killer. The cornerstones of sepsis care remain early recognition, adoption of a systematic evidence-based bundle of care, and timely escalation to higher level of care. The bundle approach has been advocated since 2004 but underwent major modifications in subsequent years with more emphasis on the time-critical nature of sepsis and need to restore physiological variables within one hour of recognition. A shift from a three and six-hour bundle to one-hour bundle has been recommended. This single hour approach has been faced with an outcry and been challenged. Over several decades, the individual components of the sepsis bundle have not changed. Encountering a patient with suspected sepsis, one should measure lactate, obtain blood cultures, swiftly administer broad spectrum antimicrobials and fluids, and infuse vasopressors. A critical question arises: should we do this for all patients? Sepsis is not septic shock and guidelines did not make distinctive recommendations for each. Septic patients will present differently with some having more subtle signs and symptoms. Phenotypically, we do not know which patient with infection will develop a dysregulated host response and will succumb to sepsis and/or shock. The existing bundle lacks high quality evidence to support its recommendations and a blanket implementation for all patients with 'suspected' sepsis could be harmful. Indeed, a significant reduction of sepsis and septic shock in Australia and New Zealand was observed in a bundle-free region. Upon arrival in the ED, patients will be triaged. This is 'time zero'. Those with hypotension and hypoperfusion will be easily recognised and at most need to receive emergent care. Sepsis, per se, may not manifest clear cut signs and expertise to identify it is required. Those with non-specific symptoms may trigger an early warning scoring system and receive unnecessary antimicrobials and a large volume of intravenous (IV) fluids. Both therapies are not without significant side effects. Putting pressure on ED physicians to implement the 60-minute bundle without individualisation of care puts our patients at risk. Given the heterogenous nature and diverse pathobiological pathways, sepsis diagnosis can be challenging and both over and under-treatment can result. Established biomarkers such as procalcitonin and C-reactive protein lack specificity to rule out infection as the cause of inflammation. Currently, no laboratory test or biomarker helps predict which patients with infection or inflammation will develop organ dysfunction. A dire need for a specific sepsis biomarker exists. Modern molecular-based technologies are evolving and utilise polymerase chain reaction (PCR), nanotechnology, and microfluidics for point-of-care testing. Some devices identify causative microorganisms and their sensitivity in less than an hour. Catecholamines along with IV fluids are indicated to restore perfusion. However, inadvertent side effects may arise, especially at higher doses. Anti-adrenergic ß-blockers improve cardiac performance, enhance receptor responsiveness, and possess anti-inflammatory action. All are desirable in patients with septic shock. One randomised trial showed beneficial and protective effects of ß-blockers in septic shock. Rapidly acting titratable agents should be used in conjunction with appropriate hemodynamic monitoring and after adequate volume resuscitation. There is no consensus on target heart rate but an arbitrary cut off of 80-95 beats per minute is reasonable. Fluid resuscitation is the cornerstone of sepsis management. There is also compelling evidence that too much fluid is bad. Starch-based colloids should not be used in septic shock. Albumin is an alternative when large volumes are required but is not appropriate in traumatic brain injury. Balanced, less chloride and less acidic crystalloids are safer for the kidneys and are preferred over normal saline. Doses of IV fluids should be tailored to the patient's condition and a 30 ml/kg recommendation should be reviewed. Effective sepsis management requires adequate dosing of antimicrobials. Significant alteration of pharmacokinetics and pharmacodynamics is characteristic of septic shock. Accurate and effective dosing is challenging particularly in patients with multiple comorbidities and those receiving extracorporeal organ support. Underdosing results in treatment failure, whilst overdosing leads to toxicity and the risk of developing multi-drug resistant organisms. An individualised approach supported by therapeutic drug monitoring is suggested to ensure clinical efficacy. The search for a cure for sepsis is ongoing. A large prospective, randomised two-arm, parallel group study aims to recruit over 200 patients with septic shock across critical care units in Qatar. Evaluation of Hydrocortisone, Vitamin C, and Thiamine (HYVITS) examines the safety and efficacy of this triple therapy. Children are particularly vulnerable to sepsis. 1 in 6 children admitted with septic shock to ICU will die. As the majority of paediatric sepsis cases are community acquired, there is a strong need to raise awareness both for families and primary healthcare providers. Akin to adults, a bundle-approach to paediatric sepsis is strongly encouraged. National programs for paediatric sepsis have been established. The Qatar paediatric multidisciplinary sepsis program was established under the umbrella of the adult programme in 2017. A structured and standardised approach to sepsis across all neonate and paediatric facilities has been developed and implemented. Improvement in timely sepsis recognition and administration of antimicrobials within the golden hour has been observed. The program aims to achieve a 95% compliance to the paediatric sepsis bundle by the end of 2019. A screening tool and order set have been put in place and are presented in this special issue of Qatar Medical Journal. Pregnancy and childbirth are risk factors for sepsis. Multi-organ failure and death can result from puerperal sepsis. Sepsis is the direct and leading cause of maternal mortality in the UK. Attention to maternal sepsis with a tailored approach is encouraged. The Qatar National Sepsis Program developed a sepsis care pathway for pregnant women and during their early post-partum period. A broader, national -or better yet- a global approach to further sepsis management and outcome should be considered. There are a number of significant challenges to address. One such challenge is the inconsistency of the operational definition and diagnostic approaches for sepsis including coding and documentation. Significant deficiencies in healthcare systems have been highlighted by sepsis. This is most obvious in medium- and low-income countries. A major limitation to effective sepsis management is inadequate medical staffing and poor knowledge and awareness of sepsis. Both have a negative impact on sepsis outcome. Poor medical facilities in many countries pose significant challenges to sepsis care. Lack of critical care capacity - a global phenomenon - has been linked to poor outcome of sepsis cases and septic shock. This could be attributed to provision of suboptimal critical care, monitoring and critical interventions outside of the ICU. ICU availability is subject to inconsistency and inequity. Lack of adequate surgical capacity to accomplish timely source control adversely affects sepsis management. This, unfortunately, in medium- and low-income countries, is accompanied by inadequate medical supplies, diagnostic capacity, and manpower which increases sepsis mortality and morbidity. Antimicrobials are critical for sepsis care. A global concern is the development of multi-drug resistant organisms and the lack of novel antimicrobials and this adds pressure on those caring for septic patients. Effective antimicrobials should be utilised to eradicate infections. Misuse, inadequacy, inferior agents, and lack of timely access to effective and affordable agents significantly hinders patient's recovery from sepsis. Optimum sepsis outcome mandates attention to acute sepsis complications (e.g. acute renal or respiratory failure) as well as addressing post-discharge complications and disability. These challenging issues remain poorly studied or addressed. Sepsis and septic shock are major global health concerns. Progress has been achieved in understanding this life-threatening syndrome at a biological, metabolic, and cellular level. Efforts should be coordinated to improve sepsis care. Better and more accurate diagnostics are needed and governments are encouraged to invest in sepsis research and care. More integrated, inclusive, and focused research is desperately needed. Public education and increased awareness among primary healthcare providers are also critical to improve sepsis outcome.

摘要

脓毒症是一种医疗急症和危及生命的病症,由宿主对感染的异常反应导致急性器官功能障碍引起。脓毒症是各个年龄层和国家的主要杀手,仍然是重症监护病房(ICU)收治和死亡的最常见原因。其真实发病率难以捉摸,对全球脓毒症负担的估计仍只是粗略猜测。一项研究表明,每年有超过1900万例病例和500万例与脓毒症相关的死亡。为应对这一挑战,世界卫生组织(WHO)世界卫生大会通过了一项关于更好地预防、诊断和管理脓毒症的决议。尽管有成千上万篇文章和数百项试验,但脓毒症仍然是主要杀手。脓毒症护理的基石仍然是早期识别、采用基于循证的系统护理方案以及及时升级到更高水平的护理。自2004年以来一直提倡采用护理方案,但在随后几年中进行了重大修改,更加强调脓毒症的时间紧迫性以及在识别后一小时内恢复生理变量的必要性。已建议从三小时和六小时护理方案转变为一小时护理方案。这种单小时方案遭到了强烈抗议并受到了挑战。几十年来,脓毒症护理方案的各个组成部分没有改变。遇到疑似脓毒症患者时,应测量乳酸水平、进行血培养、迅速给予广谱抗菌药物和液体,并输注血管加压药。一个关键问题出现了:我们应该对所有患者都这样做吗?脓毒症并非感染性休克,指南并未针对两者做出不同的建议。脓毒症患者的表现各不相同,有些患者的体征和症状更为隐匿。从表型上看,我们不知道哪些感染患者会出现宿主反应失调,并会死于脓毒症和/或休克。现有的护理方案缺乏高质量证据来支持其建议,对所有“疑似”脓毒症患者一概而论地实施可能有害。事实上,在一个没有护理方案的地区,澳大利亚和新西兰的脓毒症和感染性休克病例显著减少。患者到达急诊科后,将进行分诊。这是“零时间”。低血压和灌注不足的患者很容易被识别出来,最多只需接受紧急护理。脓毒症本身可能不会表现出明显的体征,需要专业知识来识别。有非特异性症状的患者可能会触发早期预警评分系统,并接受不必要的抗菌药物和大量静脉输液。这两种治疗方法都有明显的副作用。迫使急诊科医生在没有个性化护理的情况下实施60分钟护理方案会使我们的患者处于危险之中。鉴于脓毒症的异质性和多样的病理生物学途径,其诊断可能具有挑战性,过度治疗和治疗不足都可能发生。降钙素原和C反应蛋白等既定生物标志物缺乏特异性,无法排除感染是炎症的原因。目前,没有实验室检查或生物标志物能够帮助预测哪些感染或炎症患者会发生器官功能障碍。迫切需要一种特异性的脓毒症生物标志物。基于现代分子的技术正在不断发展,并利用聚合酶链反应(PCR)、纳米技术和微流控技术进行床旁检测。一些设备能够在不到一小时的时间内识别致病微生物及其敏感性。儿茶酚胺与静脉输液一起用于恢复灌注。然而,可能会出现意外的副作用,尤其是在高剂量时。抗肾上腺素β受体阻滞剂可改善心脏功能,增强受体反应性,并具有抗炎作用。所有这些对感染性休克患者都是有益的。一项随机试验表明,β受体阻滞剂对感染性休克具有有益和保护作用。应在适当的血流动力学监测和充分的容量复苏后,使用快速起效的可滴定药物。对于目标心率没有共识,但将每分钟80 - 95次的任意界限作为合理范围是合理的。液体复苏是脓毒症管理的基石。也有令人信服的证据表明,过多的液体是有害的。淀粉基胶体不应在感染性休克中使用。在需要大量液体时,白蛋白是一种替代选择,但不适用于创伤性脑损伤。平衡的、含氯和酸性较低的晶体液对肾脏更安全,比生理盐水更可取。静脉输液的剂量应根据患者的情况进行调整,3×10⁴/ml的推荐剂量应重新审视。有效的脓毒症管理需要给予足够剂量的抗菌药物。脓毒症休克的特点是药代动力学和药效学发生显著改变。准确有效的给药具有挑战性,特别是对于患有多种合并症的患者以及接受体外器官支持的患者。给药不足会导致治疗失败,而给药过量会导致毒性反应以及产生多重耐药菌的风险。建议采用治疗药物监测支持的个体化方法以确保临床疗效。寻找脓毒症的治疗方法的工作仍在继续。一项大型前瞻性、随机双臂、平行组研究旨在招募卡塔尔各重症监护病房的200多名感染性休克患者。氢化可的松、维生素C和硫胺(HYVITS)评估研究了这种三联疗法的安全性和有效性。儿童特别容易患脓毒症。每6名入住ICU的感染性休克儿童中就有1名会死亡。由于大多数儿科脓毒症病例是社区获得性的,因此迫切需要提高家庭和初级医疗保健提供者的认识。与成人一样,强烈鼓励采用护理方案来治疗儿科脓毒症。已经建立了国家儿科脓毒症项目。卡塔尔儿科多学科脓毒症项目于2017年在成人项目的框架下成立。已经制定并实施了针对所有新生儿和儿科设施的结构化、标准化脓毒症治疗方法。在黄金小时内对脓毒症的及时识别和抗菌药物的使用方面已有改善。该项目旨在到2019年底实现对儿科脓毒症护理方案95%的依从性。已经制定并在本期《卡塔尔医学杂志》上发表了一种筛查工具和医嘱集。怀孕和分娩是脓毒症 的危险因素。产褥期脓毒症可导致多器官功能衰竭和死亡。脓毒症是英国孕产妇死亡的直接和主要原因。鼓励采用量身定制的方法关注孕产妇脓毒症。卡塔尔国家脓毒症项目为孕妇及其产后早期制定了脓毒症护理路径。应该考虑采用更广泛的、全国性的——或者更好的是——全球性的方法来进一步管理脓毒症并改善其治疗结果。有许多重大挑战需要应对。其中一个挑战是脓毒症的操作定义和诊断方法不一致,包括编码和记录。脓毒症凸显了医疗系统的重大缺陷。这在中低收入国家最为明显。有效管理脓毒症的一个主要限制是医疗人员不足以及对脓毒症的知识和认识匮乏。这两者都对脓毒症的治疗结果产生负面影响。许多国家的医疗设施简陋给脓毒症护理带来了重大挑战。缺乏重症监护能力——这是一个全球现象——与脓毒症病例和感染性休克的不良治疗结果有关。这可能归因于提供的重症监护、监测和ICU以外的关键干预措施不理想。ICU的可用性存在不一致和不公平的情况。缺乏足够的手术能力来及时实现源头控制会对脓毒症管理产生不利影响。不幸的是,在中低收入国家,这还伴随着医疗用品、诊断能力和人力不足的问题,这增加了脓毒症的死亡率和发病率。抗菌药物对脓毒症护理至关重要。全球关注的一个问题是多重耐药菌的出现以及新型抗菌药物的缺乏,这给护理脓毒症患者的人员增加了压力。应使用有效的抗菌药物来根除感染。抗菌药物的滥用、不足、质量不佳以及缺乏及时获得有效且负担得起的药物的途径,都严重阻碍了患者从脓毒症中康复。脓毒症的最佳治疗结果要求关注急性脓毒症并发症(如急性肾或呼吸衰竭)以及解决出院后的并发症和残疾问题。这些具有挑战性的问题仍然研究不足或未得到解决。脓毒症和感染性休克是全球主要的健康问题。在从生物学、代谢和细胞水平理解这种危及生命的综合征方面已经取得了进展。应协调各方努力以改善脓毒症护理。需要更好、更准确的诊断方法,鼓励政府投资于脓毒症研究和护理。迫切需要更综合、更具包容性和更有针对性的研究。公众教育以及提高初级医疗保健提供者的认识对于改善脓毒症治疗结果也至关重要。

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