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Copyright ©The Author(s) 2023.
World J Crit Care Med. Sep 9, 2023; 12(4): 204-216
Published online Sep 9, 2023. doi: 10.5492/wjccm.v12.i4.204
Table 1 Basic characteristics of studies on early initiation of vasopressors included in the systematic review
No.
Ref.
Study design and period
No.of patients/early/late group
Agents
Time 0
Definition for early initiation
Primary outcome reported
Primary outcome
Other points
Comments
1Beck et al[31], 2014, CanadaMulticenter, retrospective cohort study 1996-20086514/-/-NE, Dopamine, Phenyleph-rine, VP, EpinephrineSurvival to hospital dischargeA weak correlation between vasopressor delay and hospital mortality (adjusted OR 1.02/h, P < 0.001)The significance was found between the delay to vasopressor initiation (> 14 h post hypotension) and the occurrence of organ failure1 Markedly delayed initiation of vasopressor (> 14 h after hypotension) in septic shock patients is associated with a small increase in mortality risk. 2 Delays in vasopressor initiation is only weakly associated with mortality, while delays in antimicrobial is more higher
2Bai et al[61], 2014, ChinaTwo centers, retrospective cohort study, Jan. 2011-Dec. 2012213/86/127NESeptic shock onsetNE administered within 2 h after onset of septic shock28 d mortalityThe early group was lower than the late group, 29.1% vs 43.3%, P < 0.0011 Duration of NE was significantly shorter in the early-NE group (2.6 ± 0.6 d vs 2.9 ± 1.0 d, P = 0.001). 2 Serum lactate levels at 2, 4, 6 and 8 h after septic shock onset were significantly lower in the early-NE group (P < 0.05)1 Early administration (within 2 h after the septic shock onset) of NE in septic shock patients is associated with an increased survival rate. 2 Early NE initiation can increase MAP, shorten the duration of hypotension and, improve vital organ perfusion and decrease serum lactate levels
3Permpikul et al[39], 2019, ThailandSingle center, RCT, Oct. 2013-Mar. 2017310/155/155NEED arrivalMedian time from emergency room arrival to NE administration was 93 minShock control rateEarly NE administration resulted in significant higher shock control rate than standard treatment, 76.1% vs 48.8%, P < 0.0011 Achievement of target MAP (> 65 mmHg), urine output (> 0.5 mL/kg) and lactate clearance (> 10%) were all significantly higher in the early-NE group (all P < 0.05). 2 There was no difference between groups for the rates of mechanical ventilator support or RRT. 3 patients in the early-NE group had a lower rate of cardiogenic pulmonary edema (14.4% vs 27.7%, P = 0.004) and new-onset arrhythmia (11% vs 20%, P = 0.03)This study confirms that the early use of NE, can enable septic shock patients to benefit in short-term endpoints, such as shock control rate, urine output and lactate clearance, represented both macro- and micro-circulation restoration
4Colon et al[62], 2019, United StatesSingle center, retrospective cohort study Jan. 2017-Jul. 2017119/76/43Vasopress-orsInitial hypotensionReceived vasopressor within 6 h from initial hypotension30 d mortalityVasopressor initiation after 6 h from shock onset is associated with a significant increase in 30 d mortality, 25% vs 51.1%, P < 0.011 Logistic regression analysis: administration of vasopressors after 6 h from hypotension were independently associated with increased 30 d mortality. 2 The time to target MAP was shorter in the early vasopressor group (1.5 h vs 3 h, P < 0.01)1 Demonstrates that there is a mortality benefit with early use of vasopressor. 2 Early administration of vasopressor in septic shock patients (< 6 h from initial hypotension) is associated with decreased mortality, that is likely secondary to faster achievement of MAP goals
5Elbouhy et al[63], 2019, EgyptSingle center, RCT Jan. 2017-Dec. 2018101/57/44NEED admissionNE infusion started after 25 (20-30) min from ED admission, simultaneous administration of crystalloid fluidsIn-hospital survivalEarly NE in septic shock improved in-hospital survival, 71.9% vs 45.5%, P = 0.0071 MAP of 65 mmHg was achieved after 2 h in the early group compared to 3 h in the late group (P = 0.003). 2 Post-resuscitation serum lactate level was 2 mmol/L in the early group and 2.9 mmol/L in the late group (P = 0.037). 3 Acute kidney injury developed in 24 of the early group (42%) compared to 23 of the late group (52%) (P = 0.3). 4 Patients in the early group were resuscitated by significantly lower volume of fluids, 25 mL/kg compared to 32.5 mL/kg in the late group (P = 0.000). 5 The in-hospital survival rate in the early group was 71.9% compared to 45.5% in the late group (P = 0.007)1 They found that early use of NE initiated simultaneously with fluids was associated with earlier achievement of target MAP, earlier lactate clearance with earlier achievement of lactate < 2 mmoL/L and consequently higher in-hospital survival. 2 The significantly lower volume required for fluids resuscitationin the early-NE than in the late-NE group
6Ospina-Tascón et al[64], 2020, ColombiaSingle center, prospective cohort study, Jan.2015-Feb.2017186/93/93NE, VPFirst resuscitative fluid loadVasopressor support initiated within the next hour or even before the first fluid load with resuscitative intention (FRLoad)Association between early vasopressor and 28 d mortalityEarly vasopressor was associated with a significant reduction in the risk of death compared to delayed vasopressor (HR 0.31, 95%CI 0.17-0.57, P < 0.001) at day 281 Patients in the early vasopressor group received less resuscitation fluids in the first 8 h of resuscitation (P < 0.001). 2 There were no significant differences regarding the maximal dose of NE, steroids and VP use, or requirement of RRT. 3 No cases of severe digital or severe vasopressor-induced splanchnic ischemia were documented1 Early vasopressor support is associated with less use of resuscitation fluids, less fluid accumulation, and shortening of hypotension time. 2 Early vasopressor was not associated with increased kidney injury or ischemia-related adverse effects, and it might decrease mortality in patients with septic shock
7Yeo et al[65], 2021, KoreanMulticenter, prospective observational study Sep. 2019-Feb. 2020298/149/149NE, VP, epinephrine, dopamineFirst resuscitative fluid loadVasopressor was initiated within 1 h of the first resuscitative fluid load28 d mortalityVasopressor initiation within 1 h was associated with higher 28 d mortality, 47.7% vs 33.6%, P = 0.0131 Volume of fluid given within the initial 6 h was significantly lower in the early group (P = 0.046). 2 The total SOFA score on day 3 in ICU was significantly lower in the late group than that in the early group (P = 0.045). Lactate levels were significantly lower on day 3 in the late group than that in the early group (P = 0.014)1 Use of a vasopressor within 1 h of the first fluid loading was related to higher mortality in patients with septic shock. 2 Less fluid was administered to the early group, but inadequate fluid resuscitation exhibited worse organ function and lactate clearance 3 d after septic shock onset
8Jouffroy et al[50], 2022, FranceMulticenter, retrospective study, Apr. 2016-Dec. 2020478/143/335NEPrehospitalPatients with prehospital NE administration (early NE)30 d mortalityPrehospital NE infusion (early NE) is associated with a decrease in 30 d mortalityN/AA strength of this study is that NE administration is started within 1 h after septic shock onset and before the completion of the fluid resuscitation
9Xu et al[7], 2022, United StatesSingle center, retrospective observational cohort study 2008-20192862/1431/1431NESeptic shock onsetReceiving NE within the first 3 h28 d mortalityEarly group had lower 28 d mortality, 30.0% vs 37.8%, P < 0.001Patients in the early-NE initiation group had a significantly shorter duration of ICU and hospital stay, shorter duration of supportive NE and invasive mechanical ventilation, lower incidence of acute kidney injury, and lower proportion of organ failure progression than patients in the delayed NE initiation groupNE initiation within the first 3 h, regardless of preload dependency, was associated with longer survival time and shorter duration of supportive NE and invasive mechanical ventilation and may delay or partially reverse rapid onset organ failure
SumUSA 2, other countries 12 RCTs11081/2190/2377NE 5Shock onset 3, ED arrival 2, First fluid 2, Prehospital 1Within 2, 3 and 6 h after shock, Within 0, 0.5, 1 h of fluid start, Prehospital28 d mortality 4 and 30 d mortality 2 hospital survival 2Mortality was lower in early group in 7 studies; mortality in early group was 28.1%-47.7%, in control group was 33.6%-54.5%