| Abstract|| |
Background: Post-cardiotomy vasoplegia syndrome (VS) is often linked to an exaggerated inflammatory response to cardiopulmonary bypass (CPB). At the same time, the prognostic role of platelet-leucocyte indices (PLIs) and leucocyte indices (LIs), (platelet-lymphocyte ratio [PLR], systemic immune-inflammation index [SII = platelet × neutrophil/lymphocyte], aggregate index of systemic inflammation [AISI = platelet × monocyte × neutrophil/lymphocyte], and neutrophil-lymphocyte ratio [NLR], systemic inflammation response index [SIRI = monocyte × neutrophil/lymphocyte), respectively] has been recently described in diverse inflammatory settings.
Methods: The retrospective study was conducted to evaluate the VS predictive performance of PLIs and LIs in 1,045 adult patients undergoing elective cardiac surgery at a tertiary care center. VS was defined by mean blood pressure <60 mmHg, low systemic vascular resistance (SVRI <1,500 dynes.s/cm 5/m2), a normal or high CI (>2.5 L/min/m2), and a normal or reduced central filling pressure despite high-dose vasopressors.
Results: About 205 (19.61%) patients developed VS postoperatively. On univariate analysis, age, diabetes, dialysis-dependent renal failure, preoperative congestive heart failure (CHF), the European System for Cardiac Operative Risk Evaluation (EuroSCORE) II, ejection fraction, NLR, PLR, SII, SIRI, AISI, CPB, and aortic cross clamp (ACC) duration, packed red blood cell (PRBC) transfusion, and time-weighted average blood glucose predicted VS. Subsequent to the multivariate analysis, the predictive performance of EuroSCORE II (OR: 3.236; 95% CI: 2.345–4.468; P < 0.001), CHF (OR: 1.04; 95% CI: 1.02–1.06; P = 0.011), SII (OR: 1.09; 95% CI: 1.02–1.18; P = 0.001), AISI (OR: 1.11; 95% CI: 1.05–1.17; P < 0.001), PRBC (OR: 4.747; 95% CI: 2.443–9.223; P < 0.001), ACC time (OR: 1.003; 95% CI: 1.001–1.005; P = 0.004), and CPB time (OR: 1.016; 95% CI: 1.004–1.028; P = 0.001) remained significant. VS predictive cut-offs of SII and AISI were 1,045 1045×109 /mm3 and 137532×109/mm3, respectively. AISI positively correlated with the postoperative vasoactive-inotropic score (R = 0.718), lactate (R = 0.655), mechanical ventilation duration (R = 0.837), and ICU stay (R = 0.757).
Conclusions: Preoperative elevated SII and AISI emerged as independent predictors of post-cardiotomy VS.
Keywords: Aggregate index of systemic inflammation, cardiac surgery, neutrophil-lymphocyte ratio, platelet-lymphocyte ratio, systemic immune-inflammation index, systemic inflammation response index, vasoplegia syndrome
|How to cite this article:|
Magoon R, Kashav RC, Shri I, Dey S, Walian A, Kohli JK. VASOplegia is Predicted by Preoperative Platelet-LEucocyte conGlomerate Indices in Cardiac Surgery (VASOPLEGICS): A retrospective single-center study. Ann Card Anaesth 2022;25:414-21
|How to cite this URL:|
Magoon R, Kashav RC, Shri I, Dey S, Walian A, Kohli JK. VASOplegia is Predicted by Preoperative Platelet-LEucocyte conGlomerate Indices in Cardiac Surgery (VASOPLEGICS): A retrospective single-center study. Ann Card Anaesth [serial online] 2022 [cited 2022 Dec 6];25:414-21. Available from: https://www.annals.in/text.asp?2022/25/4/414/358135
| Introduction|| |
The platelet-leucocyte interactions are being increasingly implicated as pivotal perpetrators of an ongoing systemic inflammatory state. As an extension of the aforementioned, there is an ever-growing interest in evaluating the prognostic role of various novel platelet-leucocyte indices (PLIs, including the platelet-lymphocyte ratio (PLR), systemic immune-inflammation index (SII = platelet × neutrophil/lymphocyte), aggregate index of systemic inflammation (AISI = platelet × monocyte × neutrophil/lymphocyte)) in diverse clinical settings predisposed to inflammation.,,,,
While a systemic inflammatory-response syndrome is inexorably associated with the conduct of cardiopulmonary bypass (CPB),, the burden of the resultant inflammatory complications can be significant. In this context, post-CPB vasoplegia syndrome (VS) is a peculiar hemodynamic complication with a wide reported incidence ranging from 9 to 40% and is heralded by systemic hypotension accompanied by a low vascular resistance, normal to augmented cardiac index, and poor response to volume therapy., Vascular hyporesponsiveness, accentuated vasopressor requirements, and heightened operative morbidity-mortality frequently compound such clinical scenarios.
Ahead of the range of demographic, pharmacological, and perioperative factors which have been described to be related to an escalated risk of post-CPB VS, the inflammatory links of VS continues to be strengthened in the recent literature.,, Herein, the description of the association of post-cardiac transplant VS with an elevated preoperative neutrophil-lymphocyte ratio (NLR) by Ahmed et al. and the elucidation of higher post-coronary artery bypass grafting vasoactive-inotropic scores (VIS) in patients with an elevated pre-grafting SII is intriguing. Therefore, we conducted the present retrospective analysis aimed at evaluating the potential of novel PLIs (PLR, SII, and AISI) and leucocyte indices (LIs, including NLR and systemic inflammation response index [SIRI = monocyte × neutrophil/lymphocyte]) in predicting post-cardiotomy VS.
| Methods|| |
After obtaining clearance from the institutional ethics committee (No. 454 (103/2020) IEC/ABVIMS/RMLH), the study was conducted at our tertiary care cardiac center. A total of 1,316 consecutive patients (age >18 years) undergoing elective cardiac surgery on CPB between January 1, 2015, and December 31, 2019, were primarily included. The patients with the presence of any one of the following conditions were excluded: anemia with hemoglobin (Hb) <10 g/dL on admission, multiple organ dysfunction syndrome (MODS defined as the development of physiologic derangement involving two or more organ systems), presence of an active infection and unavailability of complete hemogram within 48 h prior to surgery. During the intraoperative period, 86 patients required either intra-aortic balloon pump (IABP) (n = 68) or extracorporeal membrane oxygenation (ECMO) (n = 18) to assist the separation from CPB and were excluded from the analysis. Patients requiring deep hypothermic circulatory arrest during the procedure were also excluded. Another 37 patients were lost due to the unavailability of adequate postoperative data. Finally, 1,045 patients were evaluated for the outcome and their data were extracted from an electronic database and/or hospital record archive files. The flow chart for patient enrolment is illustrated in [Figure 1].
|Figure 1: The flow diagram depicting the patient enrolment with the inclusion and exclusion criteria.|
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Preoperative characteristics of the patients such as age, sex, body surface area (BSA), smoking history, pre-existing comorbidities (hypertension, diabetes mellitus [DM]), hyperlipidemia, chronic obstructive pulmonary disease, history of myocardial infarction, chronic renal failure, cerebrovascular accident, peripheral vasculopathy, and pre-existing congestive heart failure (CHF) were noted. The European System for Cardiac Operative Risk Evaluation (EuroSCORE) II was calculated using the calculator provided on the official website (http://www.euroscore.org).
Among the preoperative blood investigations (blood samples collected 24 h prior to surgery as institutional protocol), Hb, total leucocyte count (TLC), differential leucocyte count (DLC), platelet count, aspartate transaminase (AST), alanine transaminase (ALT), blood urea nitrogen (BUN), and serum creatinine values were recorded. From the following hematological indices were derived: NLR, PLR, SII, SIRI, and AISI.
Apart from these, the left ventricular ejection fraction (LVEF) documented in the preoperative echocardiography report was recorded. A detailed history of the preoperative medication intake (including angiotensin-converting enzyme inhibitor and/or angiotensin receptor blockers (ACEI/ARBs), β-blockers, calcium channel inhibitors, nitrates, aspirin, hydralazine, levothyroxine (l-T4), injectable insulin, heparin, statin, steroids (any route), digoxin, α-blockers, and diuretics was also recorded.
A standard institutional anesthetic induction, monitoring, and maintenance protocol was followed. All the patients were ventilated employing a volume-controlled mode with oxygen in the air (fraction of inspired oxygen 0.6) and a positive end-expiratory pressure of 5 cm H2O targeted to achieve an end-tidal carbon dioxide level of 35 mmHg. The intraoperative hemodynamic parameters were maintained within 20% of the baseline. Systemic heparinization was achieved with 4 mg/kg heparin and the activated clotting time (ACT) was maintained >380 s. A standard CPB institution and management regimen was followed in every patient after achieving the target ACT. After aortic and venous cannulation, an aortic cross-clamp (ACC) was placed and the heart was arrested with del Nido cardioplegia (@20 mL/kg). A maximum flow of 2.2–2.5 L/min/m2 of BSA was employed and a target perfusion pressure of 60–80 mmHg was maintained with mild-to-moderate hypothermia. A hematocrit of 24% was maintained during CPB with the addition of packed red blood cell (PRBC) when required.
Following the operative procedure, the ACC was removed and after adequate it is deairing and rewarming (temperature ≥35°C), ventilation was gradually started, and the patient was weaned off CPB slowly with the support of inotropes and vasopressor infusions. While a combination of 5 μg/kg/min dobutamine and 0.05 μg/kg/min adrenaline was initiated at rewarming, the subsequent inotrope and vasopressor management was aided by the transesophageal echocardiographic examination and/or minimally-invasive cardiac output evaluation (FloTrac™, Edwards Lifesciences, Irvine, CA, USA) with the objective of maintaining the biventricular performance and systemic perfusion. Temporary epicardial pacing was instituted as and when required. After hemodynamic stability was achieved, protamine (dose @ 1:1 of heparin) was administered. Blood and blood products were transfused to maintain Hb ≥10 g/dL. Post-sternal closure, all patients were shifted to the postoperative intensive care unit (ICU) for elective mechanical ventilation.
The following perioperative parameters were recorded: cardiac index (CI), systemic vascular resistance index (SVRI), intraoperative blood glucose (time-weighted average of blood glucose [TWAG] calculated as the area under the curve of all intraoperative glucose measurements divided by the time between the first and last measurements), number of PRBC units transfused, blood lactate, dose of the vasotropes and inotropes (calculated as VIS = Dopamine (μg/kg/min) + dobutamine (μg/kg/min) + milrinone (μg/kg/min) × 10 + epinephrine (μg/kg/min) × 100 + norepinephrine (μg/kg/min) × 100 + vasopressin (units/kg/min)×10,000), duration of CPB, ACC time, duration of mechanical ventilation (DO-MV), length of ICU stay (LOS-ICU), and length of hospital stay (LOS-H). Hemodynamic parameters were recorded at every 15-min interval intraoperatively and on an hourly basis in the ICU.
VS (within the first 24 postoperative ICU hours) was defined by the constellation of the following hemodynamic criteria: hypotension (defined by systemic mean blood pressure <60 mmHg), low systemic vascular resistance (SVRI <1,500 dynes.s/cm5/m2), a normal or high CI (>2.5 L/min/m2), and a normal or reduced central filling pressure (central venous pressure <10 mmHg) despite high-dose vasopressors (typically 0.5 μg/kg/min of norepinephrine equivalents)., Other outcomes including mortality, atrial fibrillation (AF), and acute kidney injury (AKI defined in accordance with the Acute Kidney Injury Network [AKIN] criteria) developed during the hospital stay were also noted.
The categorical variables were expressed as the number of patients and percentage of patients and compared between the groups using the Chi-square test. The continuous variables were reported as mean and standard deviation and compared between the VS and non-VS groups using the unpaired t-test. The correlation between the continuous variables was measured with the help of Pearson's correlation analysis. The non-parametric receiver operating characteristic (ROC) curve analysis was performed to evaluate the accuracy of various variables to predict VS indicated by their respective area under the curve (AUC). The “optimum cut-off point” was determined, as the cut-off point with the highest ([sensitivity + specificity]/2) ratio, at which there was a maximal correct classification of developing VS. The sensitivity, specificity, and predictive values were depicted using these generated cut-offs. The multivariate analysis was performed using the binary logistic regression method. The statistical software SPSS version 20 (IBM Corp., Armonk, NY, USA) was used for the analysis. An alpha level of 5% has been considered with any P value < 0.05 considered as significant (a Bonferroni correction was done for testing the five indices together during the multivariate analysis and P value < 0.01 was taken as significant).
| Results|| |
The study included a total of 1,045 patients out of which 205 patients developed VS (19.6%). The patient demographics, comorbid conditions, and perioperative variables have been compared in [Table 1] between VS and non-VS groups. The patients in the VS group were significantly older than the non-VS group (P < 0.001). A higher proportion of the vasoplegic patients were diabetic, suffering from dialysis-dependent renal failure and preoperative CHF had significantly poorer LVEF and higher EuroSCORE II as compared to the non-vasoplegics [Table 1]. Among the intraoperative variables, significantly higher CPB, and ACC time, higher CI, PRBC requirement, and TWAG were noted among the VS group whereas the SVRI was significantly lower in the same [Table 1]. Subsequently, univariate analysis revealed both the causative and protective factors for developing VS [Table 2]A.
|Table 1: Patient characteristics and perioperative variables for VS and non-VS groups|
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After adjusting all these factors in the multivariate analysis, the following variables remained significantly associated with the development of VS: EuroSCORE II (OR: 3.236; 95% CI: 2.345–4.468; P < 0.001), history of preoperative CHF (OR: 1.04; 95% CI: 1.02–1.06; P = 0.011), preoperative SII (OR: 1.09; 95% CI: 1.02–1.18; P = 0.001), and AISI (OR: 1.11; 95% CI: 1.05–1.17; P < 0.001), PRBC used (OR: 4.747; 95% CI: 2.443–9.223; P < 0.001), ACC time (OR: 1.003; 95% CI: 1.001–1.005; P = 0.004), and CPB time (OR: 1.016; 95% CI: 1.004–1.028; P = 0.001) [Table 2]B. Preoperative β-blocker usage was found to be protective against the development of VS (OR: 0.893; 95% CI: 0.803–0.987; P = 0.026) [Table 2]B. Metoprolol was used predominantly in our institution. However, the dosage required to protect from vasoplegia could not be determined due to the unavailability of data.
Subsequently, the ROC analysis for the hematological parameters revealed the cut-off values for predicting the development of post-CPB VS with AISI having the highest AUC (0.965) as depicted in [Figure 2]. The derived cut-off values of the hematological parameters for the development of VS were the following: NLR = 4.125 (94.6% sensitivity, 76.9% specificity); PLR = 152.635 (97.1% sensitivity, 80.9% specificity); SII = 845 (94.7% sensitivity, 85.3% specificity); SIRI = 1045 (90.7% sensitivity, 93.3% specificity), and AISI = 137,532 (90.2% sensitivity, 96% specificity).
|Figure 2: Receiver operating characteristic (ROC) curves of LIs and PLIs for predicting postoperative vasoplegia. (a) The comparison of the ROC curves of the LIs (NLR and SIRI) with respect to the area under the curve (AUC). (b) The comparison of the ROC curves of the PLIs (PLR, SII, and AISI) with respect to the area under the curve (AUC). The cut-off values, sensitivity, specificity, AUC, and 95% confidence intervals (CI) of the different hematological indices are displayed in the lower right corner of the respective figures|
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In addition, evaluation of the postoperative variables outlined a significantly higher incidence of postoperative AF (16.58% vs. 9.84%, P value = 0.006), AKI (12.68% vs. 8.23%, P value = 0.048), higher mortality rate (11.7% vs. 3.49%, P value < 0.001), a higher postoperative maximum lactate level (12.41 ± 2.03 vs. 10.47 ± 1.21, P value < 0.001), and VIS (24.64 ± 2.81 vs. 18.06 ± 1.44, P value < 0.001) and a significantly higher DO-MV (19.96 ± 6.82 vs. 15.35 ± 3.52, P value < 0.001) and LOS-ICU (4.77 ± 1.43 vs. 2.96 ± 0.84, P value < 0.001) in the VS group as compared to the non-VS group [Table 3]A. The two hematological indices which emerged as independent predictors of VS (SII and AISI) strongly positively correlated with the postoperative outcomes. The Pearson's correlation coefficients were higher for AISI (R = 0.837 for correlation with DO-MV; R = 0.757 for correlation with LOS-ICU; R = 0.718 for correlation with VIS and R = 0.655 for correlation with lactate level) [Table 3]B.
| Discussion|| |
The findings of the index study regarding the VS risk factors are largely in agreement with the seminal meta-analysis in this research area by Dayan and colleagues. Alongside the commonly implicated demographic, comorbid status, pharmacological and intraoperative surgical duration, the present study also discovered the role of the modifiable factors such as TWAG and PRBC transfusion in modulating the subsequent risk of developing VS [Table 2]A and [Table 2]B. With respect to the prognostic inflammatory hematological indices, we delineated the LIs and PLIs as important predictors of post-cardiotomy VS wherein the predictive potential of SII and AISI was robust to multivariate analysis in our evaluation.
Talking of the VS risk predictive potential of hematological inflammatory indices, the findings of the study by Ahmed et al. involving heart transplant recipients (a cohort highly predisposed to VS) deserve a mention. The retrospective study evaluated 70 patients undergoing a heart transplant with 25.7% developing vasoplegia postoperatively. Pre-transplant NLR emerged as an independent risk factor (OR 2.47) for developing VS with a mean NLR value of 6.72 among their patients manifesting VS. Our study also derived an NLR cut-off value of 4.125 for predicting post-cardiotomy VS. While Ahmed et al. attributed the high NLR value in the VS group to a pre-existing low-grade inflammation inexorably linked to a pre-transplant heart failure setting, the index study also discovered preoperative CHF as an independent predictor of developing VS. Moreover, the patients with preoperative CHF in the present study also had a significantly higher mean preoperative AISI and SII values as compared to the rest of the patient cohort (mean AISI [CHF: 155,321.89, non-CHF: 76,241.72], P value < 0.001); mean SII ([CHF: 987.25 × 103/mm3, non-CHF: 620.48 × 103/mm3], P value = 0.002).
At the same time, the literature is accumulating on the role of LIs and PLIs in predicting poor outcome following adult cardiac surgery. Herein, Rosalia et al. in their retrospective analysis of a large adult cardiac surgical cohort revealed the association of an elevated SII with postoperative outcomes albeit failed to account for the extent of poor outcome related to the development of VS. Our description of the VS risk prediction potential of SII and AISI highlights vasoplegia as an important harbinger of the prognostic links of these novel LIs and PLIs with inflammation being the common denominator. Nevertheless, our VS predictive SII cut-off value of 1,045 × 109/mm3 was higher than the Dey et al. and Rosalia et al. outcome predictive SII cut-off of 878.057 × 109/mm3 and 647, respectively.
The interaction of the corpuscular lineages with each other and the endothelium as the perpetrators of an ongoing inflammatory process continue to captivate interest.,, Ahead of the neutrophil activation and neutrophil-endothelial interactions in the inflammatory states, the neutrophil nitric oxide synthase can have pathological implications pertinent to the development of post-cardiotomy VS.,, In addition, alongside the recognition of platelets as the key players in systemic inflammation, an enhanced platelet-leucocyte cross-talk in proinflammatory states compounds the matter. Moreover, the perioperative factors such as poor glucose homeostasis and blood transfusion are also expected to activate the leucocytes and platelet-leucocyte interactions, contributing to an accentuated risk of VS, as outlined in the index analysis.,
To the best of our knowledge, the present study is a maiden endeavor at analyzing the vasoplegia predictive performance of LIs and PLIs in a cardiac surgical subset. First, the inclusion of a large sample size from a single tertiary cardiac care center constitutes a major strength of the study. Future prospective evaluation is warranted to extrapolate the findings to the highly predisposed settings like mechanical circulatory assistance. Moreover, the heterogeneity of the VS definition employed in the literature presents a unique impediment to the sound extrapolation of a novel finding in this dynamic research area., Second, the categorization of the patients as vasoplegic on the persistence of the VS-defining hemodynamic criteria in the ICU, is a positive study attribute, particularly when an isolated immediate post-CPB evaluation is precluded by a weaning-associated dynamic preload and pharmacological alterations. Third, the cost-effective readily available hematological VS risk prediction can aid in the VS risk stratification and clinical decision-making. However, the prognostic assessment in the present retrospective analysis could have been limited by the residual confounding.
| Conclusion|| |
Preoperative PLIs can potentially stratify the adult cardiac surgical subset with regards to their risk of developing post-cardiotomy VS. The aforementioned parsimonious risk stratification reemphasizes the inflammatory association of this intriguing hemodynamic syndrome.
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Conflicts of interest
There are no conflicts of interest.
| References|| |
Wagner DD, Burger PC. Platelets in inflammation and thrombosis. Arterioscler Thromb Vasc Biol 2003;23:2131-7.
Osadnik T, Wasilewski J, Lekston A, Strzelczyk J, Kurek A, Gonera M, et al
. The platelet-to-lymphocyte ratio as a predictor of all-cause mortality in patients with coronary artery disease undergoing elective percutaneous coronary intervention and stent implantation. J Saudi Heart Assoc 2015;27:144–51.
Gungor H, Babu AS, Zencir C, Akpek M, Selvi M, Erkan MH, et al
. Association of preoperative platelet-to lymphocyte ratio with atrial fibrillation after coronary artery bypass graft surgery. Med Princ Pract 2017;26:164–8.
Agus HZ, Kahraman S, Arslan C, Yildirim C, Erturk M, Kalkan AK, et al
. Systemic immune-inflammation index predicts mortality in infective endocarditis. J Saudi Heart Assoc 2020;32:57-64.
Magoon R. Evolving spectrum of prognostic inflammatory markers in infective endocarditis. J Cardiothorac Vasc Anesth 2020;34:2001-2.
Fois AG, Paliogiannis P
, Scano V, Cau S, Babudieri S, Perra R, et al
. The systemic inflammation index on admission predicts in-hospital mortality in COVID-19 patients. Molecules 2020;25:5725.
Magoon R, Makhija N. Endothelial glycocalyx and cardiac surgery: Newer Insights. J Cardiothorac Vasc Anesth 2020;34:310-1.
Magoon R, Malik V, Makhija N. Micro RNAs in cardiac surgery: Novel molecular signatures! J Cardiothorac Vasc Anesth 2020;34:570.
Byrne JG, Leacche M, Paul S, Mihaljevic T, Rawn JD, Shernan SK, et al
. Risk factors and outcomes for “vasoplegia syndrome” following cardiac transplantation. Eur J Cardiothorac Surg 2004;25:327–32.
Gomes WJ, Carvalho AC, Palma JH, Teles CA, Branco JN, Silas MG, et al
. Vasoplegic syndrome after open heart surgery. J Cardiovasc Surg 1998;39:619–23.
Carrel T, Englberger L, Mohacsi P, Neidhart P, Schmidli J. Low systemic vascular resistance after cardiopulmonary bypass: Incidence, etiology, and clinical importance. J Card Surg 2000;15:347–53.
Levin MA, Lin HM, Castillo JG, Adams DH, Reich DL, Fischer GW. Early on-cardiopulmonary bypass hypotension and other factors associated with vasoplegic syndrome. Circulation 2009;120:1664–71.
Boyle EM, Pohlman TH, Johnson MC, Verrier ED. Endothelial cell injury in cardiovascular surgery: The systemic inflammatory-response. Ann Thorac Surg 1997;63:277–84.
Tsiouris A, Wilson L, Haddadin AS, Yun JJ, Mangi AA. Risk assessment and outcomes of vasoplegia after cardiac surgery. Gen Thorac Cardiovasc Surg 2017;65:557-65.
Ahmed N, Gandhi H, Rahgozar K, Guo S, Sun E, Saeed O, et al
. Elevated pre-transplant neutrophil to lymphocyte ratio is associated with increased vasoplegia syndrome in cardiac transplantation. J Heart Lung Transplant 2019;38(Suppl. 4):S211.
Dey S, Kashav R, Kohli JK, Magoon R, Itishri, Walian A, et al
. Systemic immune-inflammation index predicts poor outcome after elective off-pump CABG: A retrospective, single-center study. J Cardiothorac Vasc Anesth 2021;35:2397-404.
Lee S, Nam S, Bae J, Cho YJ, Jeon Y, Nam K. Intraoperative hyperglycemia in patients with an elevated preoperative C-reactive protein level may increase the risk of acute kidney injury after cardiac surgery. J Anesth 2021;35:10-9.
Gaies MG, Gurney JG, Yen AH, Napoli ML, Gajarski RJ, Ohye RG, et al
. Vasoactive-inotropic score as a predictor of morbidity and mortality in infants after cardiopulmonary bypass. Pediatr Crit Care Med 2010;11:234-8.
Shaefi S, Mittel A, Klick J, Evans A, Ivascu NS, Gutsche J, et al
. Vasoplegia after cardiovascular procedures-pathophysiology and targeted therapy. J Cardiothorac Vasc Anesth 2018;32:1013-22.
Dayan V, Cal R, Giangrossi F. Risk factors for vasoplegia after cardiac surgery: A meta-analysis. Interact Cardiovasc Thorac Surg 2019;28:838-4.
Rosalia RA, Klincheva M, Klimkarov M, Zimoski R, Hristov N, Milojevik P, et al
. The systemic immune-inflammation index is associated with early postoperative morbidity and mortality following cardiac surgery. Eur Heart J 2020;41:3151.
Magoon R, Jain A. Hematological inflammatory prognostication in COVID-19: Points to ponder! Am J Emerg Med 2021;45:565-6.
Chan JL, Kobashigawa JA, Aintablian TL, Dimbil SJ, Perry PA, Patel JK, et al
. Characterizing predictors and severity of vasoplegia syndrome after heart transplantation. Ann Thorac Surg 2018;105:770-7.
Saini R, Singh S. Inducible nitric oxide synthase: An asset to neutrophils. J Leukoc Biol 2019;105:49-61.
Wachtfogel YT, Kucich U, Greenplate J, Gluszko P, Abrams W, Weinbaum G, et al
. Human neutrophil degranulation during extracorporeal circulation. Blood 1987;69:324-30.
Alfirevic A, Xu M, Johnston D, Figueroa P, Koch CG. Transfusion increases the risk for vasoplegia after cardiac operations. Ann Thorac Surg 2011;92:812–9.
Magoon R, Makhija N, Das D. Vasoplegic syndrome after cardiac surgery: Better the devil you know! J Card Surg 2019;34:1679-80.
Magoon R, Jose J. Safeguarding anaesthesia research from spin. Br J Anaesth 2020;125:e460-2. doi: 10.1016/j.bja. 2020.08.042.
Department of Cardiac Anaesthesia, Atal Bihari Vajpayee Institute of Medical Sciences (ABVIMS) and Dr. Ram Manohar Lohia Hospital, Baba Kharak Singh Marg, New Delhi - 110 001
Source of Support: None, Conflict of Interest: None
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]