Ma Cheng-Hsin, Healy Jack, Kinteh Ebrima, Ma Cheng-Chin, Tzeng Ching-Fang Tiffany, Chou Eric H, Wu Chin-Chieh, Shao Shih-Chieh, Chen Kuan-Fu
Department of Medical Education, Linkou Chang Gung Memorial Hospital, 5 Fu-Shin Street, Gueishan district, Taoyuan, 333, Taiwan.
Burnett School of Medicine, Texas Christian University, Fort Worth, TX, USA.
Ann Intensive Care. 2025 Jan 27;15(1):18. doi: 10.1186/s13613-025-01428-0.
The optimal timing for initiating vasopressor therapy in patients with septic shock remains unclear. This study aimed to assess the impact of early versus late vasopressor initiation on clinical outcomes.
A systematic review and meta-analysis were conducted by searching PubMed, Embase, and Cochrane databases. Studies comparing early and late vasopressor administration in septic shock patients were included. The primary outcome was short-term mortality, and subgroup analyses were performed based on different initiation timings.
Eleven studies with 6,661 patients were included. Different studies define the 'early administration' timeframe variously, ranging from one to seven hours. No significant difference in short-term mortality was observed between early and late administration in the combined analysis of 3,757 patients from two RCTs and three quasi-experimental studies (OR: 0.66, 95% CI: [0.36, 1.19], I²: 82%). However, lower mortality was found in subgroups with early but not extremely early initiation (one to three hours, OR: 0.70, 95% CI: [0.60, 0.82], I²: 0%), and those using septic shock diagnosis as time zero (OR: 0.64, 95% CI: [0.48, 0.85], I²: 39%).
Our findings found that earlier initiation of vasopressor therapy, particularly within one to three hours after the diagnosis of septic shock, may be associated with reduced short-term mortality in certain subgroups. However, due to the heterogeneity in study definitions and potential confounding factors, these results should be interpreted cautiously. Further standardized investigations are warranted to precisely determine the optimal timing for vasopressor initiation to maximize survival outcomes in patients with septic shock.
脓毒性休克患者开始使用血管升压药治疗的最佳时机仍不明确。本研究旨在评估早期与晚期开始使用血管升压药对临床结局的影响。
通过检索PubMed、Embase和Cochrane数据库进行系统评价和荟萃分析。纳入比较脓毒性休克患者早期和晚期使用血管升压药的研究。主要结局是短期死亡率,并根据不同的开始时机进行亚组分析。
纳入了11项研究,共6661例患者。不同研究对“早期给药”时间范围的定义各不相同,从1小时到7小时不等。在两项随机对照试验和三项准实验研究的3757例患者的综合分析中,早期和晚期给药的短期死亡率无显著差异(比值比:0.66,95%置信区间:[0.36, 1.19],I²:82%)。然而,在早期但并非极早期开始给药(1至3小时,比值比:0.70,95%置信区间:[0.60, 0.82],I²:0%)以及以脓毒性休克诊断为时间零点的亚组中,死亡率较低(比值比:0.64,95%置信区间:[0.48, 0.85],I²:39%)。
我们的研究结果发现,更早开始使用血管升压药治疗,尤其是在脓毒性休克诊断后1至3小时内,可能与某些亚组的短期死亡率降低有关。然而,由于研究定义的异质性和潜在的混杂因素,这些结果应谨慎解释。有必要进行进一步的标准化研究,以精确确定血管升压药开始使用的最佳时机,从而使脓毒性休克患者的生存结局最大化。