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Impact and Beneficial Critical Points of Clinical Outcome in Corticosteroid Management of Adult Patients With Sepsis: Meta-Analysis and GRADE Assessment

机译:对成年脓毒症患者糖皮质激素治疗的影响及临床结局的关键点:荟萃分析和GRADE评估

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摘要

>Background: With new randomised pieces of evidence and the latest clinical practice guideline from the BMJ emerging in 2018, an updated analysis of best available evidence on the controversial effects of corticosteroids in sepsis is warranted.>Objectives: To comprehensively evaluate whether corticosteroids are beneficial in reducing mortality and what cumulative dosage, daily dosage, and duration of corticosteroid treatment would enable adult patients with sepsis to reach the critical point of benefits.>Methods: Ovid MEDLINE, Ovid EMbase, Cochrane Library, and LILACS database were searched until March 22, 2019.>Results: Thirty RCTs with 8,836 participants were identified. Long course low-dose corticosteroid therapy could improve 28-day mortality (RR = 0.90, 95% CI = 0.84–0.97; high quality), intensive care unit mortality (RR = 0.87; 95% CI = 0.79–0.95; moderate quality), and in-hospital mortality (RR = 0.88, 95% CI = 0.79–0.997; high quality). However, we found no benefits for 90-day, 180-day, and 1-year mortality. Subgroup results of long course corticosteroid treatment in a population with septic shock and vasopressor-dependent septic shock, corticosteroid regimen with hydrocortisone plus fludrocortisone, corticosteroid dosing strategies including bolus dosing and infusion dosing, the strategies of abrupt discontinuation, timing of randomisation ≤24 h, impact factor of ≥10, and sample size ≥500 were associated with a marginally reduction in 28-day mortality.>Conclusions: This meta-analysis found that the long course low-dose and not short course high-dose corticosteroid treatment could marginally improve short-term 28-day mortality with high quality, especially septic shock and vasopressor-dependent septic shock, and it is recommended that long course (about 7 days) low-dose (about 200–300mg per day) hydrocortisone (or equivalent) with cumulative dose (at least about 1,000mg) may be a viable management option for overall patients with sepsis, and it can be also adapted to patient with septic shock alone. Early hydrocortisone plus fludrocortisone administration, via continuous infusion or bolus dosing, is also particularly important for the prognosis. Abrupt discontinuation of corticosteroids, as opposed to the conventional tapered discontinuation, may be considered as a desirable option in 28-day mortality. The safety profile of long course low-dose corticosteroid treatment, including adverse hyperglycaemia and hypernatraemia events, remains a concern, although these events could be easily treated.>Clinical Trial Registration: PROSPERO, identifier CRD 42018092849.
机译:>背景:有了新的随机证据和BMJ于2018年发布的最新临床实践指南,就对糖皮质激素在败血症中引起争议的最佳可用证据进行了最新分析。 ::全面评估皮质类固醇激素是否有助于降低死亡率,以及皮质类固醇激素治疗的累积剂量,每日剂量和持续时间将使成年败血症患者达到获益的临界点。>方法:搜索了Ovid MEDLINE,Ovid EMbase,Cochrane库和LILACS数据库,直到2019年3月22日。>结果:确定了30个RCT,共有8,836名参与者。长期低剂量皮质类固醇激素疗法可改善28天死亡率(RR = 0.90,95%CI = 0.84-0.97;高质量),重症监护病房死亡率(RR = 0.87; 95%CI = 0.79-0.95;中等质量) ,以及院内死亡率(RR = 0.88,95%CI = 0.79-0.997;高质量)。但是,我们发现90天,180天和1年死亡率无益处。在感染性休克和依赖于升压药的脓毒性休克人群中长期应用皮质类固醇治疗的亚组结果,氢化可的松加氟可的松皮质类固醇治疗方案,包括大剂量给药和输注给药的皮质类固醇给药策略,突然停用策略,随机化治疗时间≤24h,影响因子≥10和样本量≥500与28天死亡率略有降低有关。>结论:该荟萃分析发现,长期低剂量而非长期高剂量-剂量的皮质类固醇激素治疗可以改善高质量的短期28天死亡率,尤其是败血性休克和依赖于升压药的败血性休克,建议长期服用(约7天)小剂量(每天约200-300mg)氢化可的松(或同等水平)的累积剂量(至少约1,000mg)可能是所有败血症患者的可行治疗选择,它也可以适应于患者•仅伴有败血症性休克。通过连续输注或推注给药,早期氢化可的松加氟可的松的给药对预后也特别重要。与常规的锥形停药相反,皮质类固醇的突然停药被认为是28天死亡率的理想选择。尽管可以很容易地治疗,但长期低剂量皮质类固醇治疗的安全性(包括不良高血糖和高钠血症事件)仍然值得关注。>临床试验注册: PROSPERO,标识符CRD 42018092849。

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