Abstract
The optimal order of vasopressor discontinuation during shock resolution remains unclear. We evaluated the incidence of hypotension in patients receiving concomitant vasopressin (VP) and norepinephrine (NE) based on the order of their discontinuation. In this retrospective cohort study, consecutive patients receiving concomitant VP and NE infusions for shock admitted to intensive care units were evaluated. The primary outcome was hypotension incidence following discontinuation of VP or NE (VP1 and NE1 groups, respectively). Secondary outcomes included the incidence of acute kidney injury (AKI) and arrhythmias. Subgroup analysis was conducted by examining outcomes based on the type of shock. Of the 2,035 included patients, 952 (46.8%) were VP1 and 1,083 (53.2%) were NE1. VP1 had a higher incidence of hypotension than NE1 (42.1% vs. 14.2%; P < 0.001), longer time to shock reversal (median: 2.5 vs. 2.2 days; P = .009), higher hospital [29% (278/952) vs. 24% (258/1083); P = .006], and 28-day mortality [37% (348/952) vs. 29% (317/1,083); P < 0.001] when compared with the NE1 group. There were no differences in ICU mortality, ICU and hospital length of stay, new-onset arrhythmia, or AKI incidence between the two groups. In subgroup analyses based on different types of shock, similar outcomes were observed. After adjustments, hypotension in the following 24 h and 28-day mortality were significantly higher in VP1 (Odds ratios (OR) 4.08(3.28, 5.07); p-value < .001 and 1.27(1.04, 1.55); p-value < .001, respectively). Besides, in a multivariable model, the need for renal replacement therapy (OR 1.68 (1.34, 2.12); p-value < .001) was significantly higher in VP1. Among patients with shock who received concomitant VP and NE, the VP1 group was associated with a higher incidence of hypotension in comparison with NE1. Future studies need to validate our findings and their impact on clinical outcomes.
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Introduction
Shock is a life-threatening condition associated with a high rate of mortality1,2. Shock state could be due to multiple mechanisms, including decreased cardiac output (cardiogenic), vasodilation (distributive), cardiovascular system obstruction, or reduced effective blood volume (hypovolemic)3. One of the primary interventions in the resuscitation of patients with shock states is using a combination of fluids (except in cardiogenic shock) and vasopressors to maintain perfusion to vital organs4,5,6. Vasopressin (VP) and norepinephrine (NE) are the most commonly used vasopressors for the management of shock7,8. In catecholamine-resistant patients, high doses of NE alone often fail to reverse shock. Thus, VP may be added to either raise the mean arterial pressure (MAP) or decrease the NE dosage9.
When hemodynamic status stabilizes during the shock resolution phase, vasopressor support is gradually tapered to avoid their adverse effects10. The 2016 Surviving Sepsis Campaign Guidelines recommended NE as the vasoactive agent of choice with VP as a second-line adjunct9. Meanwhile, limited evidence for vasopressor management during the deescalation phase of shock has led to controversies in the field. Bauer et al.11 suggest that VP discontinuation before NE may lead to a higher incidence of hypotension in patients recovering from septic shock while receiving concomitant VP and NE, despite the longer half-life of VP (i.e., 1–2 min for NE and 10–35 min for VP). Yet, a similar study by Sacha et al.12 observed no significant differences in hypotension incidence based on the order of vasopressors discontinuation.
In this retrospective cohort study, we hypothesize that discontinuing VP before NE is associated with an increased incidence of hypotension, acute kidney injury (AKI), and arrhythmia in patients with shock.
Materials and methods
This retrospective cohort study was approved by the Mayo Clinic Institutional Review Board (IRB) to use existing medical records among patients who had provided research authorization (approval number: 19–008,234). The need for informed consent was waived by Mayo Clinic IRB due to the minimal risk nature of the study. All methods were performed in accordance with the relevant guidelines and regulations.
Patients
Patients were eligible for study inclusion if they were, (1) at least 18 years old, (2) admitted to the ICU in Mayo Clinic, Rochester, MN from November 1st, 2007, through January 31st, 2018, (3) diagnosed with shock13, and (4) received concomitant NE and VP infusions for ≥ 1 day. We excluded patients who died within 48 h of ICU admission, were terminally ill, had VP and NE discontinued at the same time, or received additional catecholamines and/or inotropes after discontinuation of the first vasopressor. Other vasopressors were allowed if administered before the discontinuation of VP or NE. The order of vasopressor discontinuation was at the discretion of the primary intensivist.
Data collection
Data collected from electronic medical records included demographics, admitting ICU service, Charlson Comorbidity Index, type of shock (i.e., septic, cardiogenic, or hypovolemic), and hospital and ICU length of stay. Mortality was documented at ICU discharge, hospital discharge, and 28 days. Sequential Organ Failure Assessment (SOFA)14 score and mean arterial pressure (MAP) were collected at the time of ICU admission and the time of VP and NE initiation and discontinuation, shock start time, and time and extent of hypotension following discontinuation of the first vasopressor. Maximum VP and NE doses during shock, utilization of renal replacement therapies, and corticosteroids were collected. Besides, new-onset arrhythmias after discontinuation of the first vasopressor, daily serum creatinine, and urine output were documented. To assess study outcomes, treatment for hypotension after discontinuing the first vasopressor (i.e., need for fluid challenge, need for the resumption of the discontinued vasopressor, or need for increased vasopressor dose) was collected.
Study outcomes
The primary outcome was the incidence of hypotension within 24 h of discontinuation of the first vasopressor. Secondary outcomes included ICU, hospital, and 28-day mortality, ICU and hospital length of stay, ICU readmission, time to shock reversal, new-onset arrhythmias (i.e., ventricular or atrial fibrillation, and/or heart rate > 130), and incidence of AKI.
Definitions
The shock was defined as MAP < 65 mmHg and serum lactate level > 2 mmol/L. Subgroups were further clarified based on the type of shock. Septic shock was defined based on the sepsis-3 definition15. Cardiogenic shock was defined as a state of ineffective cardiac output caused by a primary cardiac disorder that resulted in both clinical and biochemical manifestations of inadequate tissue perfusion16. The hypovolemic shock was defined as a condition of tissue hypoperfusion—caused by decreased effective blood volume due to vomiting or diarrhea, severe environmental fluid loss, or rapid and massive blood loss—that led to a decline in aerobic metabolism17. Lactate was used to assess hypoperfusion in the patients that clinicians felt were probably in the shock state. Ordering lactic acid for managing shock patients in Mayo Clinic is protocolized. However, physicians can bypass the order when they believe patients are not dealing with a hypoperfusion state. Therefore, all missing lactate levels were imputed as < 2 mmol/L as the clinicians likely felt hypoperfusion was not an issue.
Shock start time (T) is determined as the first instance of MAP < 65 mmHg or serum lactate level > 2 mmol/L, whichever came first. Time zero (T0) is the time that the first vasopressor was discontinued. T1 is days from T0 to the first documented hypotension episode, discharge from ICU, or death. Shock reversal time (T2) indicated when MAP of ≥ 65 mmHg was achieved following discontinuation of all vasopressors. The time to shock reversal was calculated as the duration between T2 and T.
Hypotension was defined as MAP < 65 mmHg during the first 24 h of discontinuation of the first vasopressor requiring one or more of these interventions: (1) increase in the vasopressor dose, (2) resuming therapy with the discontinued vasopressor or other vasopressors, (3) receipt of at least 500 mL of a crystalloid bolus or 25 g of albumin.
Following the first vasopressor discontinuation time to ICU discharge, all new-onset arrhythmias (i.e., ventricular fibrillation, atrial fibrillation, and/or heart rate > 130 beats per minute) were recorded. AKI was defined based on the Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice Guidelines18 and monitored from ICU admission up to seven days after the end of vasopressors or hospital discharge, whichever came first.
Statistical analysis
Baseline demographics and clinical characteristics were summarized using counts and percentages for categorical variables and medians and interquartile ranges for continuous variables. Data distributions based on the first withheld vasopressor, VP or NE, were compared using chi-square and Fisher exact tests19 (where appropriate) for categorical variables and Wilcoxon rank-sum tests for continuous variables. Chi-square tests and Wilcoxon rank-sum tests were used to determine associations between outcomes and the first withheld vasopressor.
Cumulative incidence curves of hypotension were plotted for visualization purposes. These same comparisons were made for septic-, hypovolemic-, and cardiogenic-only shock patients. SAS version 9.4 (SAS Institute Inc., Cary, NC) was used for all analyses. A two-sided p-value < 0.05 was considered statistically significant.
Ethical approval
This retrospective cohort study was approved by the Mayo Clinic Institutional Review Board (IRB) to use existing medical records among patients who had provided research authorization (Approval No.: 19-008234).
Consent to participate
The need for informed consent was waived due to the minimal risk nature of the study.
Results
All shock patients
We initially screened 4,927 patients, of which 2,035 met all inclusion criteria after 2,876 were excluded (Fig. 1). Of those included, 952 (47%) were in the VP-discontinued-first (VP1) group, and 1,083 (53%) were in the NE-discontinued-first (NE1) group. Demographics and patient characteristics for each group are presented in Table 1. The groups had similar demographic characteristics and severity of illness (SOFA score, median 10 vs. 10; P = 0.3). VP1 patients had higher Charlson Comorbidity Index [median 5 (4,8) vs. 5 (3,7); P < 0.001], incidence of cancer [36% (343/952) vs. 30% (322/1,083); P = 0.003], sepsis [55% (521/952) vs. 41% (440/1083)], diabetes mellitus [28% (267/952) vs. 23% (251/1,083); P = 0.01], corticosteroid use [50% (473/952) vs. 33% (357/1083); P < 0.001], dialysis requirement [24% (227/952) vs. 16% (170/1,083); P < 0.001], NE dose, and lower MAP when compared to NE1 patients.
Table 2 shows the outcomes of the cohort. The VP1 group had higher incidence of hypotension [42% (401/952) vs. 14% (154/1,083); P < 0.001], longer time to shock reversal (median: 3[2, 5] vs. 2[1, 4] days; P = 0.009), higher hospital [29% (278/952) vs. 24% (258/1,083); P = 0.006], and 28-day mortality [37% (348/952) vs. 29% (317/1,083); P < 0.001] when compared with the NE1 group. There were no differences in ICU mortality, ICU, hospital length of stay, new-onset arrhythmia, or AKI incidence.
Following adjustments for age, Charlson comorbidity index, SOFA score, maximum norepinephrine dose, corticosteroid use, diabetes mellitus, sepsis, and need for dialysis, when vasopressin stopped first hypotension in the following 24 h (Odds ratio (OR) 4.08 (3.28, 5.07); p-value < 0.001) and 28-day mortality (OR 1.27 (1.04, 1.55); p-value < 0.001) was significantly higher when compared with those who stopped norepinephrine first. Besides, after adjustment for age, Charlson comorbidity index, SOFA score, and maximum norepinephrine dose, the need for renal replacement therapy (OR 1.68 (1.34, 2.12); p-value < 0.001) was significantly higher when vasopressin stopped before norepinephrine.
Subgroup: septic shock patients
The septic shock subgroup consisted of 961 patients, with 521 (54%) in the VP1 group and 440 (46%) in the NE1 group. As shown in Additional Table 1, the VP1 group had higher use of corticosteroid [63% (326/521) vs. 47% (207/440); P < 0.001], dialysis requirement [23% (121/521) vs. 18% (79/440); P < 0.001], and NE max dose [0.24 (0.13, 0.47) vs. 0.28 (0.17, 0.48) µg/kg/min; P = 0.004] than the NE1 group. The VP1 group also had higher incidence of hypotension [48% (250/521) vs. 15% (66/440); P < 0.001], along with shorter ICU [6 (3, 10) vs. 7 (4, 13); P < 0.001] and hospital length of stay [15 (9, 31) vs. 19 (10, 38); P = 0.002] as compared to the NE1 group (Additional Table 2).
Subgroup: hypovolemic shock patients
The hypovolemic shock subgroup consisted of 32 patients (Additional Table 3). VP1 patients had lower weight [74 (60, 92) vs. 100 (84, 129); P = 0.02] and higher NE max dose [0.20 (0.13, 0.28) vs. 0.10 (0.05, 0.15) µg/kg/min; P = 0.002] compared to NE1 patients. There were no significant differences in outcomes (Additional Table 4).
Subgroup: cardiogenic shock patients
There were 257 patients in the cardiogenic shock subgroup, of which 93 (36%) were in the VP1 group, and 164 (64%) were in the NE1 group. Demographics and patient characteristics for each group are presented in Additional Table 5. The VP1 group had less heart disease [28 (30%) vs. 70 (43%); P = 0.046], more diabetes mellitus [32 (34%) vs. 37 (23%); P = 0.04], and higher max NE dose [0.12 (0.09, 0.20) vs. 0.10 (0.06, 0.15) µg/kg/min; P = 0.005] than the NE1 group. The VP1 group had a higher incidence of hypotension compared to the NE1 group [24% (22/93) vs. 13% (21/164); P = 0.03], but there were no differences in other secondary outcomes (Additional Table 6).
Cumulative incidence of hypotension and shock reversal
The cumulative incidence of hypotension following the first vasopressor discontinuation is presented in Fig. 2. By day fifteen, the VP1 group had a significantly higher incidence of hypotension than the NE1 group (37% vs. 11%, P < 0.001). The cumulative incidence of shock reversal based on the first discontinued vasopressor is presented in Fig. 3. The NE1 group shock reversal was significantly higher than for VP1 patients (P = 0.01), i.e., in the NE1 group, 78.8% had shock reversal by day 15, compared to 75.7% in the VP1 group.
Among septic patients, the VP1 group had a significantly higher incidence of hypotension following the first vasopressor discontinuation relative to the NE1 group (Additional Figure 1, P < 0.001), but no difference in the incidence of shock reversal between these groups noted (Additional Figure 2, P = 0.4). In hypovolemic shock, between VP1 and NE1 groups, there was no significant difference in the incidence of hypotension (Additional Figure 3, P = 0.3) or shock reversal based on vasopressor order discontinuation (Additional Figure 4, P = 0.06). Cardiogenic shock patients were similar to septic shock patients in that there were significant differences in the cumulative incidence of hypotension based on the vasopressor discontinuation order (Additional Figure 5, P = 0.02). Still, no difference in the rate of shock reversal was seen (Additional Figure 6, P = 0.1).
Discussion
In this retrospective cohort study of ICU patients receiving concomitant VP and NE treatment for shock management, there was a higher incidence of hypotension when VP was discontinued before NE. Additionally, when VP stopped first, a longer time to shock reversal, increased hospital mortality, and increased 28-day mortality were noted when compared with discontinuation of NE first. Order of vasopressor discontinuation did not affect other clinical outcomes, including ICU and hospital length of stay, ICU readmission, ICU mortality, the incidence of new-onset arrhythmia, and AKI. Subgroup analysis of patients with septic and cardiogenic shock revealed similar conclusions, i.e., discontinuing VP before NE was correlated with a higher incidence of hypotension but not associated with other ICU-related clinical outcomes.
The Surviving Sepsis Campaign guidelines for clinical management of septic shock suggest norepinephrine as the first-line vasopressor, and vasopressin could be added in case of catecholamine-resistant hypotension9. However, these guidelines do not provide recommendations regarding vasopressor discontinuation order when patients need NE and VP simultaneously, which is likely due to the sparsity of data regarding the benefits or disadvantages of vasopressor deescalation order. Therefore, this choice is left to the clinicians' discretion. Based on the VASST trial results and similar to most clinical practices, VP was not titrated off in our study, and it was turned on and off based on patient needs20. Thus, in the VP1 group, VP was discontinued when patients' needs for NE were on a downward trajectory. On the contrary, in the NE1 group, NE was titrated off before VP was turned off.
Only limited data explicitly evaluate the discontinuation order of VP and NE in septic shock patients11,21,22. In a retrospective study, Bauer et al.11 found that those who had VP stopped first developed hypotension more frequently (56% vs. 16%; P = 0.008) and had earlier (median 1.7 vs. 7.3 h, P = 0.04) hypotension. In another large, retrospective cohort study, Sacha et al.12 evaluated 585 patients in the recovery phase of septic shock. They found no significant difference in hypotension incidence based on the discontinuation order of VP and NE (55% vs. 50%, P = 0.3). Our findings are similar to those of Bauer et al. and contribute valuable evidence to the literature by including a larger cohort of septic shock patients. In performing several subgroup analyses, we found the association between VP discontinuation and hypotension to be remarkably consistent, adding to the strength of our conclusions.
The results of this study should be interpreted in the context of varying subgroup sizes and possible confounders. Of note, septic shock was by far the largest subgroup in this study and demonstrated statistically significant differences in the primary outcome of hypotension; the next largest subgroup, i.e., cardiogenic shock, also reached statistically significant results in the primary outcome (though to a slightly lesser extent); and the smallest cohort of hypovolemic shock did not show statistically significant differences in hypotension based on vasopressor discontinuation order. It remains undetermined whether different types of shock patients respond differently to vasopressor discontinuation order or whether more statistical power is needed to elucidate commonalities among them. Thus, interpretation of our findings for the smallest subgroup, i.e., hypovolemic shock, should be made cautiously, and generalizations need to be avoided. These questions merit further investigation.
There may be several biomolecular and physiological advantages of continued VP therapy during shock resolution. VP is a cyclic nano-peptide hormone, also known as the antidiuretic hormone, that plays an important role in the cardiovascular system's homeostatic mechanisms, exhibiting multiple hormonal and osmoregulatory effects beyond its pressor activity23,24. The decrease in VP levels increases the possibility of relative VP deficiency as a critical factor in persistent vasodilatory shock25,26,27. VP administration could decrease catecholamine requirement, thus reducing their adverse effects, including arrhythmia, acrocyanosis, vasospasm. Additionally, VP administration could lead to decreased renin-aldosterone-angiotensin system and neurohormonal activation, inhibition of proinflammatory cytokines, improvement in calcium handling, and potentiation of endogenous glucocorticoids28,29,30.
Based on the previous studies indicating VP contribution to the reduction of atrial fibrillation (by sparing adrenergic stimulation provided by catecholaminergic vasopressors)13,31,32,33, we hypothesized a higher rate of arrhythmia among patients who had VP discontinued first. However, the incidence of new-onset arrhythmia was not associated with the order of vasopressor withholding in this study. This may be related to type II error caused by inadequate power in a relatively small sample size.
Likewise, previous investigations showed that sustained VP therapy could be kidney-protective34,35,36, based on VP maintenance of glomerular filtration rate and improved creatinine clearance compared with NE37,38. However, we found no such protective effect in our study as there was no significant difference in AKI incidence between VP and NE discontinued first groups. Inadequate sample size, the low sensitivity of AKI definition criteria for acute tubular injury, and a short follow-up period for AKI development could have led to this finding.
It has been proposed that the combination of VP and corticosteroids could result in shorter shock duration and improved survival in patients with sepsis39,40. Several possible biological explanations exist for these interactions, including VP binding to V1b receptors in the anterior pituitary, leading to adrenocorticotropin hormone release41. On the other hand, corticosteroids restore cytokine-mediated down-regulation of VP receptors42. This suggests a regulatory interdependence between VP and cortisol secretion when VP stimulates corticotropin production in the setting of relative adrenal insufficiency43. Nevertheless, the interaction of corticosteroids and VP in the physiologic response to and vasodilatory shock management remains controversial. We observed more corticosteroids used in the VP1 patients in all-shock and septic shock cohorts, so further studies are needed to clarify whether corticosteroids influence the higher incidence of hypotension in the discontinued VP first group. Interestingly, in septic shock cohorts, we observed that VP1 patients stayed in the ICU for less time than NE1 patients, which is inconsistent with previous studies. This may be related to more corticosteroids being used in the VP1 group44,45, thus introducing bias to the result. Corticosteroids may help in vascular sensitivity to catecholamines through an increase in adrenoceptor gene expression46. Vasopressin has also been demonstrated to increase cortisol and adrenocorticotropic hormone, potentially assisting with the relative adrenal insufficiency observed in septic shock47.
Our study should be interpreted carefully after considering its limitations. First, this is a single-center, retrospective study and therefore is less generalizable and robust than a multi-site study with randomization of vasopressor discontinuation order. Particularly, knowing that the white race comprised more than 90% of participants, our results need to be validated on other races and groups. While it is physiologically plausible to observe differences in episodes of hypotension based on different strategies in the use of vasopressors, the hard clinical outcomes, including mortality, that were statistically different between the two groups, need validation in prospective studies as we were only able to establish correlations rather than causal relationships. Second, due to a lack of protocol for the discontinuation order, the order of vasopressor discontinuation was at the bedside practitioner's discretion. As such, it could be possible that VP was discontinued before NE because of an adverse drug event or some other medically necessary reason/s rather than simply practitioner preference. This could have induced a bias in our results which need to be validated in prospective studies. A note should also be made that inotropic and cardiac support devices for patients in the cardiogenic shock subgroup were beyond the scope of this study. However, they could likely have played a critical role in patient care and recovery. Finally, this study did not investigate cost-effectiveness. Considering the expenses associated with VP48, the cost-effectiveness of continuing VP therapy for longer periods is of paramount interest.
Conclusion
In septic and cardiogenic shock patients who received concomitant VP and NE, VP discontinuation before NE was associated with a higher incidence of hypotension than with discontinuation of NE before VP. Apart from hospital and 28-day mortality rates, the discontinuation order did not correlate with other major clinical outcomes. We noted similar results in both the septic and cardiogenic shock patients.
Data availability
The data used for this research are available from the corresponding author on reasonable request and subject to Institutional Review Board guidelines.
Abbreviations
- VP:
-
Vasopressin
- NE:
-
Norepinephrine
- AKI:
-
Acute kidney injury
- VP1:
-
Vasopressin-discontinued-first
- NE1:
-
Norepinephrine-discontinued-first
- MAP:
-
Mean arterial pressure
- SOFA:
-
Sequential Organ Failure Assessment
- ICU:
-
Intensive care unit
References
Marchick, M. R., Kline, J. A. & Jones, A. E. The significance of non-sustained hypotension in emergency department patients with sepsis. Intensive Care Med. 35, 1261–1264. https://doi.org/10.1007/s00134-009-1448-x (2009).
Varpula, M., Tallgren, M., Saukkonen, K., Voipio-Pulkki, L. M. & Pettila, V. Hemodynamic variables related to outcome in septic shock. Intensive Care Med. 31, 1066–1071. https://doi.org/10.1007/s00134-005-2688-z (2005).
Gutierrez, G., Reines, H. D. & Wulf-Gutierrez, M. E. Clinical review: Hemorrhagic shock. Crit. Care 8, 373–381. https://doi.org/10.1186/cc2851 (2004).
Levy, M. M., Evans, L. E. & Rhodes, A. The surviving sepsis campaign bundle: 2018 update. Crit. Care Med. 46, 997–1000. https://doi.org/10.1097/ccm.0000000000003119 (2018).
van Diepen, S. et al. Contemporary management of cardiogenic shock: A scientific statement from the American Heart Association. Circulation 136, e232–e268. https://doi.org/10.1161/CIR.0000000000000525 (2017).
Park, S. K. et al. The effect of early goal-directed therapy for treatment of severe sepsis or septic shock: A systemic review and meta-analysis. J. Crit. Care 38, 115–122. https://doi.org/10.1016/j.jcrc.2016.10.019 (2017).
Russell, J. A. Vasopressor therapy in critically ill patients with shock. Intensive Care Med. 45, 1503–1517. https://doi.org/10.1007/s00134-019-05801-z (2019).
Thongprayoon, C. et al. Temporal trends in the utilization of vasopressors in intensive care units: An epidemiologic study. BMC Pharmacol. Toxicol. 17, 19. https://doi.org/10.1186/s40360-016-0063-z (2016).
Rhodes, A. et al. Surviving sepsis campaign: International guidelines for management of sepsis and septic shock: 2016. Intensive Care Med. 43, 304–377. https://doi.org/10.1007/s00134-017-4683-6 (2017).
Merouani, M. et al. Norepinephrine weaning in septic shock patients by closed loop control based on fuzzy logic. Crit. Care 12, R155. https://doi.org/10.1186/cc7149 (2008).
Bauer, S. R. et al. Discontinuation of vasopressin before norepinephrine increases the incidence of hypotension in patients recovering from septic shock: A retrospective cohort study. J. Crit. Care 25(362), e367–e362. https://doi.org/10.1016/j.jcrc.2009.10.005 (2010).
Sacha, G. L. et al. Hypotension Risk based on vasoactive agent discontinuation order in patients in the recovery phase of septic shock. Pharmacotherapy 38, 319–326. https://doi.org/10.1002/phar.2082 (2018).
Vincent, J. L. & De Backer, D. Circulatory shock. N. Engl. J. Med. 369, 1726–1734. https://doi.org/10.1056/NEJMra1208943 (2013).
Vincent, J. L. et al. The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med. 22, 707–710. https://doi.org/10.1007/bf01709751 (1996).
Singer, M. et al. The third international consensus definitions for sepsis and septic shock (sepsis-3). JAMA 315, 801–810. https://doi.org/10.1001/jama.2016.0287 (2016).
Lier, H., Bernhard, M. & Hossfeld, B. Hypovolemic and hemorrhagic shock. Anaesthesist 67, 225–244. https://doi.org/10.1007/s00101-018-0411-z (2018).
Khwaja, A. KDIGO clinical practice guidelines for acute kidney injury. Nephron. Clin. Pract. 120, c179-184. https://doi.org/10.1159/000339789 (2012).
Upton, G. J. Fisher’s exact test. J. R. Stat. Soc. A. Stat. Soc. 155, 395–402 (1992).
Russell, J. A. et al. Vasopressin versus norepinephrine infusion in patients with septic shock. N. Engl. J. Med. 358, 877–887. https://doi.org/10.1056/NEJMoa067373 (2008).
Hammond, D. A. et al. Discontinuation of vasopressin before norepinephrine in the recovery phase of septic shock. J. Intensive Care Med. 34, 805–810. https://doi.org/10.1177/0885066617714209 (2019).
Bissell, B. D., Magee, C., Moran, P., Bastin, M. L. T. & Flannery, A. H. Hemodynamic instability secondary to vasopressin withdrawal in septic shock. J. Intensive Care Med. 34, 761–765. https://doi.org/10.1177/0885066617716396 (2019).
Holmes, C. L., Patel, B. M., Russell, J. A. & Walley, K. R. Physiology of vasopressin relevant to management of septic shock. Chest 120, 989–1002. https://doi.org/10.1378/chest.120.3.989 (2001).
Rozenfeld, V. & Cheng, J. W. The role of vasopressin in the treatment of vasodilation in shock states. Ann. Pharmacother. 34, 250–254. https://doi.org/10.1345/aph.19066 (2000).
Morales, D. et al. Reversal by vasopressin of intractable hypotension in the late phase of hemorrhagic shock. Circulation 100, 226–229. https://doi.org/10.1161/01.cir.100.3.226 (1999).
Barrett, L. K., Singer, M. & Clapp, L. H. Vasopressin: Mechanisms of action on the vasculature in health and in septic shock. Crit. Care Med. 35, 33–40. https://doi.org/10.1097/01.CCM.0000251127.45385.CD (2007).
Landry, D. W. et al. Vasopressin deficiency contributes to the vasodilation of septic shock. Circulation 95, 1122–1125. https://doi.org/10.1161/01.cir.95.5.1122 (1997).
Russell, J. A. et al. Vasopressin compared with norepinephrine augments the decline of plasma cytokine levels in septic shock. Am. J. Respir. Crit. Care Med. 188, 356–364. https://doi.org/10.1164/rccm.201302-0355OC (2013).
Barrett, L. K. et al. Differential effects of vasopressin and norepinephrine on vascular reactivity in a long-term rodent model of sepsis. Crit. Care Med. 35, 2337–2343. https://doi.org/10.1097/01.ccm.0000281861.72907.17 (2007).
Smith, S. M. & Vale, W. W. The role of the hypothalamic-pituitary-adrenal axis in neuroendocrine responses to stress. Dialogues Clin. Neurosci. 8, 383–395 (2006).
Dunser, M. W. & Hasibeder, W. R. Sympathetic overstimulation during critical illness: Adverse effects of adrenergic stress. J. Intensive Care Med. 24, 293–316. https://doi.org/10.1177/0885066609340519 (2009).
Schmittinger, C. A. et al. Adverse cardiac events during catecholamine vasopressor therapy: A prospective observational study. Intensive Care Med. 38, 950–958. https://doi.org/10.1007/s00134-012-2531-2 (2012).
Dunser, M. W. et al. Cardiac performance during vasopressin infusion in postcardiotomy shock. Intensive Care Med. 28, 746–751. https://doi.org/10.1007/s00134-002-1265-y (2002).
Hajjar, L. A. et al. Vasopressin versus norepinephrine in patients with vasoplegic shock after cardiac surgery: The VANCS randomized controlled trial. Anesthesiology 126, 85–93. https://doi.org/10.1097/ALN.0000000000001434 (2017).
Hajjar, L. A. et al. Vasopressin versus norepinephrine for the management of septic shock in cancer patients: The VANCS II randomized clinical trial. Crit. Care Med. 47, 1743–1750. https://doi.org/10.1097/CCM.0000000000004023 (2019).
Gordon, A. C. et al. Effect of early vasopressin vs norepinephrine on kidney failure in patients with septic shock: The VANISH randomized clinical trial. JAMA 316, 509–518. https://doi.org/10.1001/jama.2016.10485 (2016).
Lauzier, F., Levy, B., Lamarre, P. & Lesur, O. Vasopressin or norepinephrine in early hyperdynamic septic shock: A randomized clinical trial. Intensive Care Med. 32, 1782–1789. https://doi.org/10.1007/s00134-006-0378-0 (2006).
Patel, B. M., Chittock, D. R., Russell, J. A. & Walley, K. R. Beneficial effects of short-term vasopressin infusion during severe septic shock. Anesthesiology 96, 576–582. https://doi.org/10.1097/00000542-200203000-00011 (2002).
Russell, J. A. et al. Interaction of vasopressin infusion, corticosteroid treatment, and mortality of septic shock. Crit. Care Med. 37, 811–818. https://doi.org/10.1097/CCM.0b013e3181961ace (2009).
Gordon, A. C. et al. The interaction of vasopressin and corticosteroids in septic shock: A pilot randomized controlled trial. Crit. Care Med. 42, 1325–1333. https://doi.org/10.1097/ccm.0000000000000212 (2014).
O’Callaghan, D. J. & Gordon, A. C. What’s new in vasopressin?. Intensive Care Med. 41, 2177–2179. https://doi.org/10.1007/s00134-015-3849-3 (2015).
Ertmer, C. et al. Methylprednisolone reverses vasopressin hyporesponsiveness in ovine endotoxemia. Shock 27, 281–288. https://doi.org/10.1097/01.shk.0000235140.97903.90 (2007).
Schurr, J. W., Szumita, P. M. & DeGrado, J. R. Neuroendocrine derangements in early septic shock: Pharmacotherapy for relative adrenal and vasopressin insufficiency. Shock 48, 284–293. https://doi.org/10.1097/SHK.0000000000000864 (2017).
Bredhold, B. E. et al. Impact of the sequence of norepinephrine and vasopressin discontinuation in patients recovering from septic shock. Hosp. Pharm. 55, 26–31. https://doi.org/10.1177/0018578718817469 (2020).
Hammond, D. A. et al. Effects of norepinephrine and vasopressin discontinuation order in the recovery phase of septic shock: A systematic review and individual patient data meta-analysis. Pharmacotherapy 39, 544–552. https://doi.org/10.1002/phar.2265 (2019).
Saito, T. et al. Corticosteroid effect on early beta-adrenergic down-regulation during circulatory shock: Hemodynamic study and beta-adrenergic receptor assay. Intensive Care Med. 21, 204–210. https://doi.org/10.1007/BF01701473 (1995).
Mutlu, G. M. & Factor, P. Role of vasopressin in the management of septic shock. Intensive Care Med. 30, 1276–1291. https://doi.org/10.1007/s00134-004-2283-8 (2004).
Hammond, D. A. et al. Perceptions regarding vasopressin use and practices in septic shock, and cost containment strategies. J. Am. Coll. Clin. Pharmacy 2, 257–267. https://doi.org/10.1002/jac5.1079 (2019).
Lam, S. W. et al. Cost-effectiveness of second-line vasopressors for the treatment of septic shock. J. Crit. Care 55, 48–55. https://doi.org/10.1016/j.jcrc.2019.10.005 (2020).
Funding
Mayo Clinic Rochester CCRS (Critical Care IMP Research Subcommittee) grant (Grant No. CCRTUVNA).
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K.K., C.W., and X.S. designed this study and protocol development; K.E. and X.L. were responsible for the data collection; R.F. and X.S. were responsible for data analysis; X.S. and X.L. conducted the manuscript writing; K.K., C.W., Y.D., E.B., C.L., and X.G. critically revising the manuscript; K.K. and X.S. final approved the version to be published. All authors agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy of any part of the work are appropriately investigated and resolved.
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Supplementary Information
Additional Table 1.
Demographics and Patient Characteristics Among Septic Shock Only.
Additional Table 2.
Clinical Outcomes of Septic Shock Only.
Additional Table 3.
Demographics and Patient Characteristics Among Hypovolemic Shock Only.
Additional Table 4.
Clinical Outcomes of Hypovolemic Shock Only.
Additional Table 5.
Demographics and Patient Characteristics Among Cardiogenic Shock Only.
Additional Table 6.
Clinical Outcomes of Cardiogenic Shock Only.
Additional Figure 1.
Cumulative incidence of hypotension following first vasopressor discontinuation among septic shock only patients.
Additional Figure 2.
Cumulative incidence of shock reversal following first vasopressor discontinuation among septic shock only patients.
Additional Figure 3.
Cumulative incidence of hypotension following first vasopressor discontinuation among hypovolemic shock only patients.
Additional Figure 4.
Cumulative incidence of shock reversal following first vasopressor discontinuation among hypovolemic shock only patients.
Additional Figure 5.
Cumulative incidence of hypotension following first vasopressor discontinuation among cardiogenic shock only patients.
Additional Figure 6.
Cumulative incidence of shock reversal following first vasopressor discontinuation among cardiogenic shock only patients.
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Song, X., Liu, X., Evans, K.D. et al. The order of vasopressor discontinuation and incidence of hypotension: a retrospective cohort analysis. Sci Rep 11, 16680 (2021). https://doi.org/10.1038/s41598-021-96322-7
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DOI: https://doi.org/10.1038/s41598-021-96322-7
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