Next Article in Journal
Impacts of Neoadjuvant Chemotherapy on Perioperative Outcomes in Patients with Bladder Cancer Treated with Radical Cystectomy: A Single High-Volume Center Experience
Next Article in Special Issue
Ultrasonographic Applications of Novel Technologies and Artificial Intelligence in Critically Ill Patients
Previous Article in Journal
Performance of a Machine Learning Algorithm to Predict Hypotension in Spontaneously Breathing Non-Ventilated Post-Anesthesia and ICU Patients
Previous Article in Special Issue
The Incidence of Perioperative Hypotension in Patients Undergoing Major Abdominal Surgery with the Use of Arterial Waveform Analysis and the Hypotension Prediction Index Hemodynamic Monitoring—A Retrospective Analysis
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Individualized Perioperative Hemodynamic Management Using Hypotension Prediction Index Software and the Dynamics of Troponin and NTproBNP Concentration Changes in Patients Undergoing Oncological Abdominal Surgery

by
Jolanta Cylwik
1,*,
Małgorzata Celińska-Spodar
1,2 and
Mariusz Dudzic
3
1
Anesthesiology and Intensive Care Unit, Mazovia Regional Hospital, 08-110 Siedlce, Poland
2
Anesthesiology and Intensive Care Unit, The National Institute of Cardiology, 04-628 Warsaw, Poland
3
Critical Care, Edwards Lifesciences, 00-807 Warsaw, Poland
*
Author to whom correspondence should be addressed.
Submission received: 15 January 2024 / Revised: 8 February 2024 / Accepted: 14 February 2024 / Published: 16 February 2024
(This article belongs to the Special Issue Personalized Medicine in Anesthesia and Anesthetics)

Abstract

:
Introduction: Abdominal oncologic surgeries pose significant risks due to the complexity of the surgery and patients’ often weakened health, multiple comorbidities, and increased perioperative hazards. Hypotension is a major risk factor for perioperative cardiovascular complications, necessitating individualized management in modern anesthesiology. Aim: This study aimed to determine the dynamics of changes in troponin and NTproBNP levels during the first two postoperative days in patients undergoing major cancer abdominal surgery with advanced hemodynamic monitoring including The AcumenTM Hypotension Prediction Index software (HPI) (Edwards Lifesciences, Irvine, CA, USA) and their association with the occurrence of postoperative cardiovascular complications. Methods: A prospective study was conducted, including 50 patients scheduled for abdominal cancer surgery who, due to the overall risk of perioperative complications (ASA class 3 or 4), were monitored using the HPI software. Hypotension was qualified as at least one ≥ 1 min episode of a MAP < 65 mm Hg. Preoperatively and 24 and 48 h after the procedure, the levels of NTproBNP and troponin were measured, and an ECG was performed. Results: We analyzed data from 46 patients and found that 82% experienced at least one episode of low blood pressure (MAP < 65 mmHg). However, the quality indices of hypotension were low, with a median time-weighted average MAP < 65 mmHg of 0.085 (0.03–0.19) mmHg and a median of 2 (2–1.17) minutes spent below MAP < 65 mmHg. Although the incidence of perioperative myocardial injury was 10%, there was no evidence to suggest a relationship with hypotension. Acute kidney injury was seen in 23.9% of patients, and it was significantly associated with a number of episodes of MAP < 50 mmHg. Levels of NTproBNP were significantly higher on the first postoperative day compared to preoperative values (285.8 [IQR: 679.8] vs. 183.9 [IQR: 428.1] pg/mL, p < 0.001). However, they decreased on the second day (276.65 [IQR: 609.4] pg/mL, p = 0.154). The dynamics of NTproBNP were similar for patients with and without heart failure, although those with heart failure had significantly higher preoperative concentrations (435.9 [IQR: 711.15] vs. 87 [IQR: 232.2] pg/mL, p < 0.001). Patients undergoing laparoscopic surgery showed a statistically significant increase in NTproBNP. Conclusions: This study suggests that advanced HPI monitoring in abdominal cancer surgery effectively minimizes intraoperative hypotension with no significant NTproBNP or troponin perioperative dynamics, irrespective of preoperative heart failure.

1. Introduction

It is estimated that approximately 300 million surgical procedures are conducted each year globally [1], of which noncardiac surgeries (NCSs) comprise roughly 85% [2]. A significant subset of these surgical interventions is dedicated to treating patients with gastrointestinal malignancies. This is because, notwithstanding the progress in chemotherapy and radiotherapy, surgical intervention continues to be a crucial component in the therapeutic regimen for these conditions.
Despite the introduction of increasingly advanced surgical techniques and a trend toward minimizing invasiveness (e.g., laparoscopy) as well as refining the precision of surgical methods (robotic techniques), patients remain susceptible to perioperative complications associated with the undergone procedure, of which cardiovascular complications are the most common [3,4,5].
In the cohort study published by Spence et al. [6] in 2019, which included 40,000 patients, it was demonstrated that in the group of patients over 45 years old undergoing NCS, serious cardiac and cerebrovascular complications occurred within 30 days of the procedure in one out of every seven patients—indicating a substantial scale of the problem. Moreover, the occurrence of major cardiovascular events (MACEs) increases the risk of mortality within 30 days post-procedure [7,8,9], and the 30-day mortality rate for patients who suffer perioperative myocardial injury (PMI) is approximately 10% [9,10].
Given the volume of surgical procedures, the prevalence of discussed complications, and their serious outcomes, contemporary anesthesiology should prioritize the monitoring and prompt treatment of cardiovascular episodes. The perioperative diagnosis of PMI presents considerable challenges due to the unique characteristics of this timeframe. Symptoms such as chest pain may be obscured by the painkillers given to patients, and conducting imaging tests can be challenging or unfeasible. In line with the European Society of Cardiology (ESC) and American Heart Association (AHA) guidelines, diagnoses should rely on perioperative surveillance. This involves the meticulous observation of changes in routine postoperative electrocardiograms and the measurement of troponin levels, a biomarker indicative of myocardial injury [8,9].
The N-terminal pro B-type Natriuretic Peptide (NTproBNP), an additional cardiac biomarker, has an increasing role in risk stratification [9]. As a critical marker of cardiac function, NTproBNP frequently elevates in response to cardiac stress or dysfunction. Alongside other natriuretic hormones, such as the Atrial Natriuretic Peptide (ANP) and Brain Natriuretic Peptide (BNP), it is synthesized in response to increased ventricular pressure or volume. Collectively, these hormones contribute to regulating fluid balance, natriuresis, and vascular resistance [9,11,12,13], and their levels correlate with the severity and prognosis of heart failure (HF) [12]. Beyond the context of HF, a preoperative elevation in NTproBNP has been associated with an augmented risk of postoperative cardiovascular events [9,14,15,16].
One of the factors most strongly associated with MACE, such as PMI or acute kidney injury (AKI), is intraoperative hypotension (IOH).
One of the methods to individualize the approach to hemodynamic management during anesthesia for elevated risk procedures to reduce the risk of intraoperative hypotension is using, beyond basic blood pressure measurements, advanced hemodynamic parameters such as stroke volume, stroke volume variation, cardiac output, and systemic vascular resistance. These parameters are derived in real-time from the shape and characteristics of the arterial waveform using proprietary algorithms [17]. In addition, applying The AcumenTM Hypotension Prediction Index software (number 02.03.000.103) (HPI) (Edwards Lifesciences, Irvine, CA, USA) for hemodynamic monitoring involves predictive analytics to foresee and prevent episodes of hemodynamic destabilization. It was developed using machine learning to predict arterial hypotension, defined as a mean arterial pressure (MAP) of less than 65 mm Hg for at least 1 min. Additionally, this technology identifies its causes, like hypovolemia, vascular resistance issues, or reduced cardiac contractility. It allows for early, tailored treatment, reducing the frequency and severity of hypotensive episodes. An intervention is recommended when the HPI reaches a threshold of 85 [5,17,18,19,20].
A series of randomized, single-center studies have indicated that the integration of the Hemodynamic Performance Index (HPI) into perioperative monitoring is associated with a reduction in intraoperative hypotension in general noncardiac surgeries. This observation was reported in the HYPE clinical trial conducted by Wijinberge et al. [21], as well as in studies focusing on major noncardiac surgeries involving populations at an elevated risk, as examined by Sribar et al. [22] and Yoshikawa et al. [23]. Complementing these findings, a non-randomized but substantial registry study, the European multi-center prospective observational EU HYPROTECT, conducted by Kouz et al. [24], also demonstrated low incidences of hypotension when using HPI. This study, involving 702 patients across 12 medical centers in five European countries, found that the median time-weighted average mean arterial pressure (MAP) < 65 mm Hg was significantly low, suggesting that HPI-software monitoring could potentially reduce the duration and severity of intraoperative hypotension in patients undergoing noncardiac surgery. Despite these findings, the current literature does not conclusively establish whether the prevention of hypotension leads to a decrease in cardiac stress, as evidenced by the dynamics of cardiac biomarkers.
This study aimed to determine the dynamics of troponin and NTproBNP concentration changes during the first two postoperative days in patients undergoing high-risk cancer abdominal surgery with advanced hemodynamic monitoring featuring HPI. The hypothesis posited that the individualized hemodynamic management and active, targeted prevention of hypotension could reduce cardiovascular complications (PMI, AKI, stroke). A secondary objective was to explore the relationship between biomarker dynamics and hypotension or hemodynamic instability, indicated by an HPI value exceeding 85%.

2. Material and Methods

2.1. Study Design

This prospective study was conducted at the Mazovia Regional Hospital, a tertiary oncologic center, from March 2023 to October 2023, involving a cohort of 50 consecutive patients scheduled for major cancer gastrointestinal surgery who met the following conditions:
Age: Participants had to be older than 18 years of age.
ASA classification: Patients classified under the American Society of Anesthesiologists Physical Status Classification System (ASA) with a status of 3 or 4 were eligible for inclusion.
Perioperative risk profile: Procedures of intermediate (≥1 to 5%) or high (>5%) surgical risk of postoperative cardiovascular complications [9] qualified.
Surgical procedure: Eligible participants were those scheduled for oncological gastrointestinal surgery.
Perioperative hemodynamic monitoring: Perioperative hemodynamic monitoring was conducted using the AcumenTM IQ sensor and the HemoSphere monitoring platform (both Edwards Lifesciences, Irvine, CA, USA)
Informed consent: Patients who provided informed consent for participation in this study qualified for inclusion.
Approval for this study was procured from the Bioethics Committee at the Regional Chamber of Physicians and Dentists in Warsaw under the reference number KB 1421/22.

2.2. Clinical Definitions

Advanced hemodynamic parameters were obtained using the HemoSphere monitoring platform, equipped with the AcumenTM IQ sensor, through minimally invasive access via a radial artery line. In addition to directly measured values obtained via an arterial line, such as arterial pressure and heart rate, the Edwards HemoSphere device utilizes specific advanced algorithms to derive a series of hemodynamic parameters. These parameters are based on the characteristics of the arterial waveform, including its shape, amplitude, and temporal changes. The derived parameters include the following [25]:
The cardiac index (CI) quantifies the cardiac output relative to body surface area, measured in liters per minute per square meter.
Stroke volume (SV) denotes the volume of blood ejected by the left ventricle during a single contraction.
The Systemic Vascular Resistance Index (SVRI) provides a normalized measure of the resistance of the systemic vasculature, adjusted for body surface area.
Stroke volume variation (SVV) indicates the fluctuation in stroke volume with each cardiac cycle.
The Rate of Change of Left Ventricular Pressure in time (dP/dt) measures the rate of pressure change in the left ventricle during systole and is a key indicator of cardiac contractility.
Dynamic Vascular Elastance (Eadyn) is a parameter indicating the responsiveness of the arterial system to changes in stroke volume. It helps in understanding the interaction between the heart and the vascular system, especially in guiding fluid therapy and vasopressor use.
The HPI (Hemodynamic Performance Index) is an advanced algorithm-based parameter that combines various hemodynamic measurements to predict the likelihood of a patient developing hypotension.
An episode of hypotension was defined as a decrease in MAP below 65 mmHg for more than 1 min. The HemoSphere monitoring platform acquired various quality indices of hypotension in real-time, which included the following:
  • The number of hypotension episodes.
  • Total duration of hypotension episodes (unit: min).
  • Average duration of each hypotension episode (unit: min).
  • The proportion of time spent in hypotension (MAP < 65 mmHg) relative to the total monitoring duration (unit: %).
  • Area Under the Threshold (AUT) (unit: mmHg × min).
  • Time-weighted average (TWA) of MAP < 65 mmHg, calculated as the area under the curve of MAP below 65 mmHg divided by the total monitoring time (unit: mmHg).
  • Number of hypotension episodes with MAP < 50 mmHg.
  • Number of episodes with an increase in the HPI value above 85.
Perioperative myocardial injury and infarction (PMI) was defined in accordance with the 2022 ESC guidelines for NCS as acute cardiomyocyte injury (postoperative high-sensitivity cardiac Troponin T/I release) with or without accompanying symptoms and with or without ECG or imaging evidence of acute myocardial ischemia [9]. In biochemical studies, this was characterized by an absolute increase in high-sensitivity cardiac Troponin T/I (e.g., the 99th percentile upper reference limit) above the preoperative high-sensitivity cardiac Troponin T/I concentration [9].
Acute kidney injury (AKI) was defined in accordance with the Kidney Disease: Improving Global Outcomes Clinical Practice Guideline for Acute Kidney Injury (KDIGO) criteria. AKI was diagnosed when the serum creatinine level increased by at least 0.3 mg/dl within 48 h post-operation relative to the baseline value or when there was an increase in the serum creatinine level of more than 50% from the baseline value during the first 7 days post-operation [26].

2.3. Perioperative Management

Patients were prepared for anesthesia and surgery based on their health status, comorbidities, and the planned operation. Advanced hemodynamic monitoring using the Acumen IQ sensor in conjunction with the HemoSphere platform and HPI technology was initiated prior to the induction of general anesthesia. This enabled the acquisition of the HPI parameter and other advanced cardiovascular dynamics parameters, including CI, SV, SVRI, SVV, dP/dt, and Eadyn (Figure 1). Anesthesia induction and maintenance were conducted according to the clinical routine of the attending anesthesiologist. After typical preoxygenation, the intravenous induction of general anesthesia was performed. Patients received fentanyl (2 mcg/kg), propofol (1.5–2.5 mg/kg, individually adjusted based on age and coexisting conditions), and rocuronium (0.6 mg/kg) for muscle relaxation. Atropine was administered during induction if indicated. Anesthesia maintenance was achieved using desflurane (MAC: 1.0–1.1) and fractional doses of rocuronium and fentanyl. Radial artery cannulation was performed after administering local anesthesia with 1 mL of 2% lignocaine (subcutaneous administration). Hemodynamic monitoring continued until the patient left the operating room. The anesthesiologists, experienced in administering general anesthesia and operating the HemoSphere platform, had received official training in the use of HPI software with the Acumen IQ sensor and the HemoSphere platform. Patient management was adapted according to the clinical routine and HPI training of the attending anesthesiologist. The algorithms trained on the Edwards Lifesciences platform, utilizing the HPI, recommend interventions when the HPI value exceeds 85. This is to prevent a drop in MAP based on current hemodynamic parameters [19,25]. Specifically, if a patient demonstrates fluid responsiveness (defined as SVV ≥ 13%) and has an Eadyn above 1.1, administering a fluid bolus of a 250 mL crystalloid is advised to increase MAP. Conversely, if SVV is 13% or higher, but Eadyn is below 1, the use of vasopressors is recommended to maintain hemodynamic stability. In cases where dP/dt is below 400, despite a normal SVV, inotropes should be administered. Furthermore, if both SVV and dP/dt are within normal ranges, but the HPI exceeds 85, an increase in the Systemic Vascular Resistance Index (SVRI) is suggested (Figure 1). Monitoring and data recording using the HPI software began before the induction of general anesthesia and concluded upon the patient’s departure from the operating room. Serum Troponin T, NTproBNP levels, and electrocardiograms were used preoperatively, then again at 24 and 48 h post-operation.

2.4. Data Collection

The analysis was based on data obtained from the patient’s medical records, including the anesthesia qualification form, surgical records, anesthesia records, postoperative monitoring records, and physician’s orders. Hypotension data, including the number of hypotension episodes, total duration of hypotension episodes, average duration of a hypotension episode, AUT, TWA for MAP < 65 mmHg, number of hypotension episodes with MAP < 50 mmHg, and number of episodes with an increase in the HPI value above 85, were obtained using the dedicated Acumen Analytics v. 2.0.0. software (Edwards Lifesciences, Irvine, CA, USA).

2.5. Statistical Analysis

The delta between parameter values was calculated as the difference between the later measurement and the earlier one (measurement at 24 h postoperatively minus the baseline measurement; measurement at 48 h postoperatively minus the baseline; measurement at 48 h postoperatively minus the measurement at 24 h postoperatively). The percentage change was calculated as the ratio of the later measurement to the earlier one, multiplied by 100%. Higher values indicate a benefit for the later parameter (its value relative to the earlier measurement was higher), whereas negative values indicate a decrease in the parameter value compared to the earlier measurement.
For quantitative variables, basic descriptive statistics were calculated with the Shapiro–Wilk test to assess the normality of the distribution. In order to compare the groups in terms of quantitative variables, the Mann–Whitney U test was utilized. The Pearson chi-squared test (for independence) or Fisher’s exact test (when the expected number was less than 5) was applied for categorical data. To determine the relationships between quantitative/ordinal variables, the Spearman’s rho correlation coefficient was used. Because the distributions of NT-proBNP and troponin were skewed, a non-parametric Friedman test was used to test for changes between preoperative, 24 h postoperative, and 48 h postoperative NT-proBNP and troponin values, and the Wilcoxon-signed-rank test for a within-patient change in NT-proBNP and troponin. A significance level of p < 0.05 was adopted for all analyses. Values of p between 0.05 and 0.10 were considered to indicate a trend, but not statistically significant. The statistical analyses were performed using IBM SPSS Statistics 28.0 software.

3. Results

3.1. Patients’ Characteristics

A total of 50 consecutive eligible patients were enrolled in this study. Four patients were excluded from the final analysis due to the lack of all required laboratory tests—consequently, the analysis was carried out for 46 patients. The majority of the study group were men (69.6%). The average age of patients was nearly 70 years, with the oldest being 86. The most common chronic diseases were hypertension (69.6%) and chronic heart failure (45.7%). Regarding the ASA scale, 65.2% of patients were classified as ASA3, and 34.8% were in the ASA4 group. The POSSUM scale scores for the patients were high, with an average risk of postoperative complications being 75.66% and a risk of postoperative death being 34.58%. More than half of the patients (54.3%) underwent preoperative chemotherapy treatment, and gastrectomy was the most common surgery performed (43.5%). Half of the procedures (50%) lasted over 4 h, and almost all patients (97.8%) required perioperative use of noradrenaline. The average initial level of NTproBNP was 641 pg/mL, with values ranging from 12.3 to 13,350.4 pg/mL. The average initial troponin level was 0.0158 μg/L, which exceeded the laboratory norm’s 99th percentile upper reference limit (n < 0.014 μg/L). The full characteristics of the study group are presented in Table 1.
Most patients in this study (N = 38, 82.6%) experienced at least one episode of hypotension. Among the eight patients who did not experience hypotension, there was a median of eight HPI alarms per surgery, suggesting effective preemptive interventions facilitated by this technology. The remaining 38 patients had an average of two hypotension episodes each, with a median of 11 HPI alarms. The median TWA of MAP < 65 mm Hg was 0.085 (IQR: 0183) mm Hg. The median number of ≥1 min episodes of a MAP < 65 mm Hg was 2 (IQR: 2.25). Patients spent a median of 1.95 (IQR: 1.87) min below MAP < 65 mmHg. The median number of ≥1 min episodes of a MAP < 50 mm was zero (Table 2). Nearly all patients (97.8%) required vasopressor support with noradrenaline, and more than one-third (37%) required a combined regimen of noradrenaline and dobutamine (Table 1).
In this cohort, PMI was observed in 5 patients (10.9%), and AKI occurred in 11 patients (23.9%) within two days postoperatively. Additionally, one patient (2.2%) exhibited postoperative symptoms of acute respiratory failure, and four patients (8.7%) presented with HF symptoms necessitating further pharmacological management. Notably, one patient (2.2%) required hospital readmission within 30 days following surgery, and there was a single instance of mortality (2.2%) within the same postoperative period. Table 3 delineates the relationship between various hypotension-related parameters and patient groups, specifically those with postoperative PMI or AKI and those with preoperatively diagnosed chronic HF. A pronounced incidence of at least one hypotension episode was noted across all cohorts, with the HF group exhibiting the greatest frequency (95% vs. 72% in patients without HF, p = 0.055). A significant finding was that patients with AKI were more likely to experience prolonged episodes (≥1 min) of MAP < 50 mmHg (11 patients with AKI had seven such episodes, in contrast to eight episodes among the 35 patients without AKI; p = 0.027). No other significant differences were identified despite the observed variability among the different patient groups. This lack of a significant difference could be attributed to the small sample sizes, potentially restricting the statistical power necessary to discern more subtle distinctions in hypotension parameters between the groups. These findings imply that either the true differences in hypotension parameters among these groups are not pronounced or that this study may lack sufficient power to detect them.

3.2. Perioperative Dynamics of NTproBNP

NTproBNP plasma concentration for the entire patient cohort was 183.9 [interquartile range (IQR): 428.1] pg/mL at baseline, increasing to 285.8 [IQR: 679.8] pg/mL at 24 h, and 276.7 [IQR: 609.4] pg/mL at 48 h post-surgery (p < 0.001). A statistically significant elevation in NTproBNP levels was noted when comparing preoperative values to those measured 24 h after surgery (p < 0.001), as well as at 48 h postoperatively (p = 0.002). However, the change in NTproBNP levels between 24 and 48 h post-surgery was not statistically significant (p = 0.154). Postoperatively, an increase in NT-proBNP was observed in 80.4% of patients. The absolute and relative increases in NTproBNP post-surgery were reported as 91.2 [IQR: 177.4] pg/mL (median, IQR) and 177.6% at 24 h, and 64.6 [IQR: 241] pg/mL and 166% at 48 h, respectively.
When analyzing data with respect to preoperative chronic heart failure, it was demonstrated that patients with diagnosed heart failure exhibited significantly higher baseline levels of NTproBNP (435 [IQR: 711.15] pg/mL, p < 0.001), as well as at 24 h (482.3 [IQR: 1067.6] pg/mL, p = 0.002) and 48 h (346 [IQR: 1180.2] pg/mL, p = 0.006) postoperatively, compared to patients without diagnosed heart failure (Table 4). Among the heart failure cohort (n = 21), the postoperative change in NTproBNP was significant (p = 0.023), with significance only between the preoperative and 24 h postoperative measurements (p = 0.023). In the non-heart-failure group (n = 25), the postoperative change in NTproBNP was also significant (p < 0.001), both between preoperative values and 24 h post-surgery (p = 0.001) and between preoperative values and 48 h post-surgery (p = 0.007), with no statistical significance in the dynamic changes between the first and second postoperative days. In patients without recognized preoperative chronic heart failure, the percentage difference in NTproBNP levels between baseline and 24 h post-surgery was greater compared to patients with a heart failure diagnosis (225.17% vs. 146.28%, p = 0.032). Table 4 presents the NTproBNP level changes for the entire study group, marked preoperatively, at 24 and 48 h post-surgery. The changes in NTproBNP levels over a 48 h period post-surgery were also analyzed in relation to the co-occurrence of chronic diseases, with no significant differences observed (see Supplementary Material, Table S1). Additionally, no correlation was found between the dynamics of NT-proBNP levels and scores on the POSSUM scale (Supplementary Material, Table S2).

3.3. Perioperative Dynamics of Troponin

Median troponin concentrations for the entire patient cohort were observed at 0.012 [IQR: 0.011] μg/L at baseline, increasing to 0.017 [IQR: 0.01075] μg/L at 24 h, and 0.0165 [IQR: 0.013] μg/L at 48 h post-surgery (p < 0.003). A statistically significant elevation in troponin concentration was observed when comparing preoperative values to those measured 24 h after surgery (p = 0.001), as well as at 48 h postoperatively (p < 0.001). The change in troponin concentration between 24 and 48 h post-surgery was not statistically significant (p = 0.767) (see Figure 2). In total, 39.1% (n = 18) of patients had an elevated baseline level of troponin. Postoperatively, an increase in troponin levels was observed in 67% of patients, and 11% (n = 5) met the criteria for perioperative myocardial injury. However, due to the absence of electrocardiogram changes, the criteria for myocardial infarction were not fulfilled. Patients with higher preoperative troponin levels experienced greater hemodynamic instability, as indicated by a higher number of HPI alarms (14 vs. 9), although this difference was not statistically significant (p = 0.313). Nevertheless, the total number of hypotension episodes and the mean duration of these episodes were similar between both groups (Supplementary Table S3).
The analysis assessed the relationship between NTproBNP change dynamics and PMI occurrence (Supplementary Table S4). The medians of NT-proBNP levels were higher in the PMI group, with the largest increase observed on the first postoperative day; however, this difference was not statistically significant (273 [IQR: 421.85] vs. 1381 [IQR: 3136.75] pg/mL in PMI, p = 0.315). Additionally, this study found no significant difference in the frequency or duration of hypotension episodes between patients with and without PMI (Table 3).

3.4. Perioperative Dynamics of NtproBNP and Acute Kidney Injury

In the study group, the frequency of acute kidney injury (AKI) was 23.9% (n = 11), with 10 patients classified in KDIGO class 1, and only 1 patient in class 2. None of the patients required renal replacement therapy. Patients who developed AKI had significantly higher baseline NT-proBNP levels (435 [IQR: 926.6] pg/mL vs. 111.4 [IQR: 294] pg/mL, p = 0.036). In these patients, a reduction in the level of this biomarker was observed over the two subsequent postoperative days; however, the change between preoperative and postoperative values was not statistically significant (p = 0.790), with a significant decrease noted between the first and second postoperative day (p = 0.006). This trend was completely different from the changes in NTproBNP levels in patients who did not develop AKI. These patients experienced a significant postoperative increase in NTproBNP concentration (p < 0.001), specifically between preoperative values and 24 h post-surgery (p < 0.001), and 48 h post-surgery (p < 0.001), but without a significant change between the first and second postoperative days (p = 1.0) (Figure 3 and Supplementary Table S5).

3.5. Perioperative Biomarkers’ Dynamic in Laparoscopic vs. Open Surgery

In total, 36.9% of the patients (n = 17) underwent minimally invasive robotic or laparoscopic surgeries in the steep Trendelenburg position (28–32 degrees). No differences were observed in the occurrence of hypotension, frequency of PMI, and AKI between these groups (Supplementary Table S6). However, a statistically significant difference was noted in the dynamics of NT-proBNP—the absolute increases in the concentration of this biomarker in the blood of patients were substantially higher in those undergoing laparoscopic surgeries (absolute and relative change: 192.2 [IQR: 592.4] pg/mL and 177.35% vs. 62.25 [IQR: 103.83] pg/mL and 168.53%, p = 0.031). No differences in the dynamics of troponin levels were noted.

4. Discussion

Abdominal oncologic surgery presents unique challenges and hazards related to an increased perioperative risk on the patient and procedural sides. Patients with cancer commonly preoperatively present with weakened health and multiple comorbidities, including cardiovascular risk factors, malnutrition, and compromised immune systems, making them more susceptible to anesthesia-related adverse events [9]. In a 2018 report from the USA National Inpatient Sample database, nearly half (44.5% of 10581621 hospitalizations for major NCS) of adults aged ≥45 years undergoing major noncardiac surgery presented with at least two major cardiovascular risk factors. Moreover, the burden of cardiovascular risk factors and their prevalence increased over time [27]. In particular, cancer surgeries can be prolonged and procedurally complicated, carrying an increased risk of the procedure itself, such as significant blood loss, deep vein thrombosis, pressure sores, and respiratory or cardiovascular instability [28].
The minimum risk associated with major adverse cardiac events in oncologic abdominal surgeries, such as colorectal surgery with bowel resection, is estimated to be high (>5%) and rises further with the increased complexity of the procedure, as in duodenal–pancreatic surgery, liver resection, or esophagectomy [8,9].
The 2014 ACC/AHA Guideline on Perioperative Cardiovascular Evaluation and Management for noncardiac surgery categorizes elevated-risk procedures when the combined surgical and patient risk of major adverse cardiac events is ≥1 percent, therefore encompassing most abdominal cancer surgeries as elevated-risk procedures [8]. Furthermore, previous cancer treatments, such as chemotherapy or radiation, can affect both the surgical and anesthesia processes, adding to the complexity of managing fluid balance and blood loss during these extensive surgeries [29,30].
This complexity, coupled with the way anesthesia can influence hemodynamic stability, underscores the need for highly skilled and tailored anesthesia management to mitigate the risks of hypotension or cardiac events in this patient population. Research primarily based on retrospective and observational studies, including meta-analyses, indicates that a MAP below 60 mmHg is associated with increased organ injury and mortality. These findings were foundational for the Perioperative Quality Initiative consensus statement on intraoperative blood pressure, published in 2019 [31], which concluded that an intraoperative MAP below 60–70 mm Hg is associated with myocardial injury, acute kidney injury, and death, noting that the extent of injury correlates with the severity and duration of hypotension. Although the optimal intraoperative blood pressure target to minimize perioperative complications remains uncertain [32], personalizing intraoperative MAP targets could significantly improve perianesthesia outcomes. However, this strategy requires further investigation to establish its effectiveness [33]. Utilizing HPI in hemodynamic monitoring software, which employs predictive analytics, has been shown to not only forecast and potentially prevent episodes of hemodynamic destabilization but also to facilitate achieving targeted blood pressures intraoperatively. Current research indicates that HPI can effectively reduce the occurrence, duration, and severity of IOH in noncardiac surgeries, particularly when standard intraoperative protocols are adhered to properly [20,21,22,23,24,34,35,36,37].
In our analysis, hypotension—defined as at least one episode of MAP < 65 mmHg lasting ≥1 min—was common, occurring in over four-fifths of the patients (82.6%). However, comparisons with other studies are challenging due to variations in how IOH is reported and measured, such as invasive versus manual monitoring and real-time versus interval-based assessments [38]. For instance, Sessler and colleagues [39] reported a 69% incidence of IOH in general noncardiac surgery among 25,702 patients, while Gregory et al. [35] observed it in 19.3% of 70,938 surgical cases, where blood pressure was measured at intervals. In contrast, data from the recent prospective observational EU Hyproject registry [24] showed that 59.4% of patients in ASA classes 1–4 experienced a MAP < 65 mm Hg for at least 1 min when assessed in real-time using the AcumenTM IQ sensor and the HemoSphere monitoring platform by Edwards Lifesciences. Compared to these studies, our cohort, predominantly of higher-risk patients classified as ASA class 3 (65.2%) or 4 (34.8%), exhibited a higher incidence of IOH. Despite the high categorical rates of experiencing MAP < 65 mm Hg for at least 1 min, paralleling EU Hyproject registry [24] results, the application of HPI software version 02.03.000.103 revealed that the median time-weighted average MAP < 65 mm Hg in our cohort was notably low, at 0.085 (IQR: 0.03–0.19) mmHg with a median of 3 min spent below a MAP of 65 mmHg.
Notably, these episodes were more prevalent in patients with heart failure (95.2%) compared to those without (72.0%), although this difference was not statistically significant (p = 0.055). There were no significant differences observed in TWA MAP < 65 mmHg (0.1 [IQR: 0.03–0.19] mm Hg vs. 0.07 [IQR: 0.03–0.19] mm Hg, respectively) or in the median time spent below 65 mm Hg (3 min for both groups). However, patients with heart failure triggered more HPI alarms, leading to more frequent interventions by anesthesiologists (11 vs. 9).
These findings suggest that incorporating HPI into perioperative care facilitates proactive management to achieve stable hemodynamics. It assists in anticipating and mitigating episodes of low blood flow, thereby reducing cardiac workload and potentially decreasing the release of cardiac stress markers such as NTproBNP.
NTproBNP’s utility extends beyond a heart failure diagnosis to various clinical contexts. While elevated BNP or NTproBNP might also indicate undiagnosed heart failure, they also rise in pulmonary diseases (e.g., pulmonary embolism, obstructive sleep apnea, chronic obstructive lung disease), neurological disorders (e.g., stroke), renal insufficiency, and other critical illnesses. However, these noncardiac conditions can induce BNP or NT-pro-BNP elevation through underlying cardiac issues [9,11,12,13,14,15,16].
In particular, preoperative NT-pro-BNP elevation is strongly linked to increased postoperative cardiovascular event risk [9,15,40]. However, interpreting postoperative NT-proBNP dynamics is more complex. An 18-study meta-analysis (n = 2179) examining pre- and postoperative Natriuretic Peptide levels found that including postoperative levels in a risk model enhanced 30-day and ≥180-day risk classification. Elevated postoperative levels, particularly above 718 (95% CI: 656–994) pg/mL, were key independent outcome predictors at both intervals [16]. In our study, the median postoperative NT-pro-BNP values were 201 (IQR: 268) pg/mL for patients without diagnosed heart failure and 482 (IQR: 1067) pg/mL for those with heart failure. These levels in both groups were below the risk threshold identified by Redseth et al. Furthermore, the average of 10 HPI alarms triggering anesthesiologist intervention per surgery in our cohort suggests the effective mitigation of detrimental volume status changes and hypotension episodes. Consequently, this individualized hemodynamic management using HPI may have contributed to reduced cardiac stress expressed as lower NT-pro-BNP elevations.
Conversely, another study examining NT-pro-BNP dynamics in young, healthy patients undergoing noncardiac surgery reported lower postoperative NTproBNP levels (median of 42 [11–86] pg/mL) and found no correlation with adverse clinical events [41]. This pattern is somewhat mirrored in our study, where patients without heart failure exhibited lower postoperative NTproBNP levels (201 pg/mL) compared to those with heart failure (482 pg/mL). However, in both groups, the postoperative shift in NTproBNP was not statistically significant when compared to preoperative values (70.9 vs. 104 pg/mL, respectively).
This suggests a link to perioperative volume status changes, indicating that subtle subsequent NTproBNP elevations may not always signify critical cardiac stress or predict adverse outcomes, particularly in healthy populations. Conversely, in patient groups with existing circulatory clinical or subclinical dysfunctions or other significant comorbidities, these transient changes in volume status could induce more substantial cardiac stress, as reflected in more pronounced NTproBNP kinetics, potentially leading to subsequent adverse events, if hemodynamic instability is not managed early. Therefore, the role of postoperative NTproBNP as a marker of impaired perioperative hemodynamics merits consideration.
This conclusion is supported by the finding that when using HPI in our study of high-risk patients, the incidence of PMI of 11% was comparable to other studies [9]. However, no association was found between PMI and the occurrence of hypotension in all cohorts, with similar levels of hypotension parameters observed regardless of PMI status. This raises the question of whether intraoperative hypotension in patients with heart failure indicates impaired circulatory autoregulation or disease severity rather than directly causing postoperative complications [32,42]. Furthermore, no neurological complications were associated with hypotension. Conversely, patients meeting the AKI criterion had more episodes of MAP < 50 mmHg than those who did not, although other hypotension parameters were consistent across both groups. This observation aligns with the concept of organ blood flow autoregulation, which maintains constant blood flow within certain MAP ranges, considered to be 50–160 mmHg for the brain [43], 70–130 mmHg for the kidneys [44], and 60–140 mmHg [45] for the myocardium. This suggests that different pressure threshold goals could be taken into consideration for the kidneys compared to the brain and heart.

5. Conclusions and Limitations

Our study found minimal intraoperative hypotension, as evidenced by brief and mild episodes of mean arterial pressure falling below 65 mmHg. Advanced hemodynamic monitoring with HPI was effective in reducing significant intraoperative hypotension episodes, both in patients with and without preoperative heart failure or elevated troponin levels. Notably, high preoperative NT-pro-BNP levels were associated with an increased risk of acute kidney injury, and laparoscopic surgery patients showed significant NT-pro-BNP level increases postoperatively. These results indicate that HPI technology can achieve hemodynamic stability in high-risk patients (ASA classes 3 and 4), reducing hypotension episodes.
This study has several limitations that should be considered when interpreting the findings. Firstly, the small sample size potentially limits the statistical power of the analysis, making it challenging to draw definitive conclusions or generalize the results to a broader population. Secondly, as a single-center study, the results might be influenced by specific practices or patient demographics unique to this center, which may not represent other settings. Thirdly, the absence of a control group in the study design limits the ability to assess the effectiveness of interventions compared to standard care or other alternative treatments. These limitations highlight the need for larger, multi-center studies with control groups to validate and expand upon our findings.

Supplementary Materials

The following supporting information can be downloaded at: https://0-www-mdpi-com.brum.beds.ac.uk/article/10.3390/jpm14020211/s1, Table S1. The changes in NTproBNP levels over a 48-hour period post-surgery and the co-occurrence of chronic diseases. Table S2. Correlations between the change in NT-proBNP between the preoperative level and the second day post-operation, and the proportions between these levels and age. Table S3. Comparison of hypotension parameters depending on the baseline troponin level. Table S4. Comparison of NT-proBNP parameters depending on meeting the PMI criterion. Table S5. Comparison of NT-proBNP parameters depending on the occurrence of AKI. Table S6. Frequency analysis along with Fisher’s exact test for the relationship between the type of surgery and the occurrence of hypotension, PMI, AKI.

Author Contributions

Conceptualization, J.C. and M.C.-S.; methodology, J.C. and M.C.-S.; software, M.C.-S. and J.C.; validation, J.C., M.D. and M.C.-S.; formal analysis, J.C. and M.C.-S.; investigation, J.C., M.D. and M.C.-S.; resources, J.C.; data curation, J.C., M.D. and M.C.-S.; writing—original draft preparation, J.C., M.D. and M.C.-S.; writing—review and editing, J.C., M.D. and M.C.-S.; visualization, J.C., M.D. and M.C.-S.; supervision, J.C.; project administration, J.C.; funding acquisition, J.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Ethics Committee of the Bioethics Committee at the Regional Chamber of Physicians and Dentists in Warsaw (protocol code KB 1421/22 on 2 February 2023).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data are available upon request from the corresponding author.

Conflicts of Interest

Jolanta Cylwik has served as a consultant for Edwards Lifesciences and has received honoraria for delivering lectures. Additionally, Mariusz Dudzic is currently an employee of Edwards Lifesciences. These affiliations have not influenced the research or its methodology, results, or conclusions in any manner. The company had no input in the design, execution, interpretation, or writing of the study. Rigorous academic and ethical standards have been strictly adhered to throughout the study, ensuring that the findings and outcomes result solely from objective scientific inquiry.

Abbreviations

NCSNoncardiac Surgery
MACEMajor Cardiovascular Event
PMIPerioperative Myocardial Injury
ESCEuropean Society of Cardiology
AHAAmerican Heart Association
NTproBNPN-terminal pro B-type Natriuretic Peptide
HFHeart Failure
AKIAcute Kidney Injury
IOHIntraoperative Hypotension
HPIThe AcumeTM Hypotension Prediction Index Software (Edwards Lifesciences, Irvine, CA, USA)
MAPMean Arterial Pressure
ASAAmerican Society of Anesthesiologists Physical Status Classification System (ASA)
KDIGOKidney Disease: Improving Global Outcomes Clinical Practice Guideline for Acute Kidney Injury
AUTArea Under the Threshold
TWATime-Weighted Average
IQRInterquartile Range

References

  1. Weiser, T.G.; Haynes, A.B.; Molina, G.; Lipsitz, S.R.; Esquivel, M.M.; Uribe-Leitz, T.; Fu, R.; Azad, T.; Chao, T.E.; Berry, W.R.; et al. Estimate of the global volume of surgery in 2012: An assessment supporting improved health outcomes. Lancet 2015, 385 (Suppl. S2), S11. [Google Scholar] [CrossRef]
  2. Eurostat. EU Population in 2020: Almost 448 Million. Available online: https://ec.europa.eu/eurostat/documents/2995521/11081093/3-10072020-AP-EN.pdf/d2f799bf-4412-05cc-a357-7b49b93615f1 (accessed on 31 March 2022).
  3. Sazgary, L.; Puelacher, C.; Lurati Buse, G.; Glarner, N.; Lampart, A.; Bolliger, D.; Steiner, L.; Gürke, L.; Wolff, T.; Mujagic, E.; et al. Incidence of major adverse cardiac events following non-cardiac surgery. Eur. Heart J. Acute Cardiovasc. Care 2021, 10, 550–558. [Google Scholar] [CrossRef]
  4. Sellers, D.; Srinivas, C.; Djaiani, G. Cardiovascular complications after non-cardiac surgery. Anaesthesia 2018, 73 (Suppl. S1), 34–42. [Google Scholar] [CrossRef]
  5. Nolde, J.M.; Schlaich, M.P.; Sessler, D.I.; Mian, A.; Corcoran, T.B.; Chow, C.K.; Chan, M.T.V.; Borges, F.K.; McGillion, M.H.; Myles, P.S.; et al. Machine learning to predict myocardial injury and death after non-cardiac surgery. Anaesthesia 2023, 78, 853–860. [Google Scholar] [CrossRef]
  6. Spence, J.; LeManach, Y.; Chan, M.T.V.; Wang, C.; Sigamani, A.; Xavier, D.; Pearse, R.; Alonso-Coello, P.; Garutti, I.; Srinathan, S.K.; et al. Vascular Events in Noncardiac Surgery Patients Cohort Evaluation (VISION) Study Investigators. Association between complications and death within 30 days after noncardiac surgery. Can. Med. Assoc. J. 2019, 191, E830–E837. [Google Scholar] [CrossRef]
  7. Weber, M.; Luchner, A.; Seeberger, M.; Mueller, C.; Liebetrau, C.; Schlitt, A.; Apostolovic, S.; Jankovic, R.; Bankovic, D.; Jovic, M.; et al. Incremental value of high-sensitive troponin T in addition to the revised cardiac index for peri-operative risk stratification in non-cardiac surgery. Eur. Heart J. 2013, 34, 853–862. [Google Scholar] [CrossRef]
  8. Fleisher, L.A.; Fleischmann, K.E.; Auerbach, A.D.; Barnason, S.A.; Beckman, J.A.; Bozkurt, B.; Davila-Roman, V.G.; Gerhard-Herman, M.D.; Holly, T.A.; Kane, G.C.; et al. 2014 ACC/AHA guideline on perioperative cardiovascular evaluation and management of patients undergoing noncardiac surgery: Executive summary: A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation 2014, 130, 2215–2245. [Google Scholar] [CrossRef] [PubMed]
  9. Halvorsen, S.; Mehilli, J.; Cassese, S.; Hall, T.S.; Abdelhamid, M.; Barbato, E.; De Hert, S.; de Laval, I.; Geisler, T.; Hinterbuchner, L.; et al. 2022 ESC Guidelines on cardiovascular assessment and management of patients undergoing non-cardiac surgery. Eur. Heart J. 2022, 43, 3826–3924. [Google Scholar] [CrossRef] [PubMed]
  10. Puelacher, C.; Lurati Buse, G.; Seeberger, D.; Sazgary, L.; Marbot, S.; Lampart, A.; Espinola, J.; Kindler, C.; Hammerer, A.; Seeberger, E.; et al. Perioperative myocardial injury after noncardiac surgery: Incidence, mortality, and characterization. Circulation 2018, 137, 1221–1232. [Google Scholar] [CrossRef] [PubMed]
  11. Kinnunen, P.; Vuolteenaho, O.; Ruskoaho, H. Mechanisms of atrial and brain natriuretic peptide release from rat ventricular myocardium: Effect of stretching. Endocrinology 1993, 132, 1961–1970. [Google Scholar] [CrossRef] [PubMed]
  12. McDonagh, T.A.; Metra, M.; Adamo, M.; Gardner, R.S.; Baumbach, A.; Böhm, M.; Burri, H.; Butler, J.; Čelutkienė, J.; Chioncel, O.; et al. 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure. Heart J. 2021, 42, 3599–3726. [Google Scholar] [CrossRef] [PubMed]
  13. Iwanaga, Y.; Nishi, I.; Furuichi, S.; Noguchi, T.; Sase, K.; Kihara, Y.; Goto, Y.; Nonogi, H. B-type natriuretic peptide strongly reflects diastolic wall stress in patients with chronic heart failure: Comparison between systolic and diastolic heart failure. J. Am. Coll. Cardiol. 2006, 47, 742–748. [Google Scholar] [CrossRef] [PubMed]
  14. Dernellis, J.; Panaretou, M. Assessment of cardiac risk before non-cardiac surgery: Brain natriuretic peptide in 1590 patients. Heart 2006, 92, 1645–1650. [Google Scholar] [CrossRef] [PubMed]
  15. Duceppe, E.; Patel, A.; Chan, M.T.V.; Berwanger, O.; Ackland, G.; Kavsak, P.A.; Rodseth, R.; Biccard, B.; Chow, C.K.; Borges, F.K.; et al. Preoperative N-terminal pro-B-type natriuretic peptide and cardiovascular events after noncardiac surgery: A cohort study. Ann. Intern. Med. 2020, 172, 96–104. [Google Scholar] [CrossRef] [PubMed]
  16. Rodseth, R.N.; Biccard, B.M.; Le Manach, Y.; Sessler, D.I.; Buse, G.A.L.; Thabane, L.; Schutt, R.C.; Bolliger, D.; Cagini, L.; Cardinale, D.; et al. The prognostic value of pre-operative and post-operative B-type natriuretic peptides in patients undergoing noncardiac surgery: B-type natriuretic peptide and N-terminal fragment of pro-B-type natriuretic peptide: A systematic review and individual patient data meta-analysis. J. Am. Coll. Cardiol. 2014, 63, 170–180. [Google Scholar] [CrossRef]
  17. Jozwiak, M.; Monnet, X.; Teboul, J.L. Pressure Waveform Analysis. Anesth. Analg. 2018, 126, 1930–1933. [Google Scholar] [CrossRef]
  18. Vos, J.J.; Scheeren, T.W.L. Intraoperative hypotension and its prediction. Indian. J. Anaesth. 2019, 63, 877–885. [Google Scholar] [CrossRef]
  19. Sidiropoulou, T.; Tsoumpa, M.; Griva, P.; Galarioti, V.; Matsota, P. Prediction and Prevention of Intraoperative Hypotension with the Hypotension Prediction Index: A Narrative Review. J. Clin. Med. 2022, 11, 5551. [Google Scholar] [CrossRef]
  20. Hatib, F.; Jian, Z.; Buddi, S.; Lee, C.; Settels, J.; Sibert, K.; Rinehart, J.; Cannesson, M. Machine-learning algorithm to predict hypotension based on high-fidelity arterial pressure waveform analysis. Anesthesiology 2018, 129, 663–674. [Google Scholar] [CrossRef]
  21. Wijnberge, M.; Geerts, B.F.; Hol, L.; Lemmers, N.; Mulder, M.P.; Berge, P.; Schenk, J.; Terwindt, L.E.; Hollmann, M.W.; Vlaar, A.P.; et al. Effect of a Machine Learning-Derived Early Warning System for Intraoperative Hypotension vs Standard Care on Depth and Duration of Intraoperative Hypotension During Elective Noncardiac Surgery: The HYPE Randomized Clinical Trial. JAMA 2020, 323, 1052–1060. [Google Scholar] [CrossRef]
  22. Šribar, A.; Jurinjak, I.S.; Almahariq, H.; Bandić, I.; Matošević, J.; Pejić, J.; Peršec, J. Hypotension prediction index guided versus conventional goal directed therapy to reduce intraoperative hypotension during thoracic surgery: A randomized trial. BMC Anesthesiol. 2023, 23, 101. [Google Scholar] [CrossRef]
  23. Yoshikawa, Y.; Maeda, M.; Kunigo, T.; Sato, T.; Takahashi, K.; Ohno, S.; Hirahata, T.; Yamakage, M. Effect of using hypotension prediction index versus conventional goal-directed haemodynamic management to reduce intraoperative hypotension in non-cardiac surgery: A randomised controlled trial. J. Clin. Anesth. 2024, 93, 111348. [Google Scholar] [CrossRef] [PubMed]
  24. Kouz, K.; Monge García, M.I.; Cerutti, E.; Lisanti, I.; Draisci, G.; Frassanito, L.; Sander, M.; Akbari, A.A.; Frey, U.H.; Grundmann, C.D.; et al. Intraoperative hypotension when using hypotension prediction index software during major noncardiac surgery: A European multicentre prospective observational registry (EU HYPROTECT). BJA Open 2023, 6, 100140. [Google Scholar] [CrossRef] [PubMed]
  25. Sun, L.S.; Davis, N.A. Cardiac Physiology. In Miller’s Anesthesia, 9th ed.; Gropper, M.A., Cohen, N.H., Eriksson, L.I., Fleisher, L.A., Leslie, K., Wiener-Kronish, J.P., Eds.; Elsevier Saunders: Philadelphia, PA, USA, 2020. [Google Scholar]
  26. Kellum, J.A.; Lameire, N.; KDIGO AKI Guideline Work Group. Diagnosis, evaluation, and management of acute kidney injury: A KDIGO summary (Part 1). Crit. Care 2013, 17, 204. [Google Scholar] [CrossRef] [PubMed]
  27. Smilowitz, N.R.; Gupta, N.; Guo, Y.; Beckman, J.A.; Bangalore, S.; Berger, J.S. Trends in cardiovascular risk factor and disease prevalence in patients undergoing noncardiac surgery. Heart 2018, 104, 1180–1186. [Google Scholar] [CrossRef] [PubMed]
  28. Mohammad Shehata, I.; Elhassan, A.; Alejandro Munoz, D.; Okereke, B.; Cornett, E.M.; Varrassi, G.; Imani, F.; Kaye, A.D.; Sehat-Kashani, S.; Urits, I.; et al. Intraoperative Hypotension Increased Risk in the Oncological Patient. Anesth. Pain. Med. 2021, 11, e112830. [Google Scholar] [CrossRef] [PubMed]
  29. Niraula, S.; Seruga, B.; Ocana, A.; Shao, T.; Goldstein, R.; Tannock, I.F.; Amir, E. The price we pay for progress A meta-analysis of harms of newly approved anticancer drugs. J. Clin. Oncol. 2012, 30, 3012–3019. [Google Scholar] [CrossRef] [PubMed]
  30. Schirrmacher, V. From chemotherapy to biological therapy: A review of novel concepts to reduce the side effects of systemic cancer treatment (Review). Int. J. Oncol. 2019, 54, 407–419. [Google Scholar] [CrossRef]
  31. Sessler, D.I.; Bloomstone, J.A.; Aronson, S.; Berry, C.; Gan, T.J.; Kellum, J.A.; Plumb, J.; Mythen, M.G.; Grocott, M.P.; Edwards, M.R.; et al. Perioperative Quality Initiative consensus statement on intraoperative blood pressure, risk and outcomes for elective surgery. Br. J. Anaesth. 2019, 122, 563–574. [Google Scholar] [CrossRef]
  32. D’Amico, F.; Fominskiy, E.V.; Turi, S.; Pruna, A.; Fresilli, S.; Triulzi, M.; Zangrillo, A.; Landoni, G. Intraoperative hypotension and postoperative outcomes: A meta-analysis of randomised trials. Br. J. Anaesth. 2023, 131, 823–831. [Google Scholar] [CrossRef]
  33. Kamenetsky, E.; Hogue, C.W. Is a Mean Arterial Pressure Less Than 65 mm Hg an Appropriate Indicator of the Quality of Anesthesia Care? Anesth. Analg. 2021, 132, 942–945. [Google Scholar] [CrossRef]
  34. de Keijzer, I.N.; Vos, J.J.; Scheeren, T.W.L. Hypotension Prediction Index: From proof-of-concept to proof-of-feasibility. J. Clin. Monit. Comput. 2020, 34, 1135–1138. [Google Scholar] [CrossRef]
  35. Gregory, A.; Stapelfeldt, W.H.; Khanna, A.K.; Smischney, N.J.; Boero, I.J.; Chen, Q.; Stevens, M.; Shaw, A.D. Intraoperative Hypotension Is Associated with Adverse Clinical Outcomes After Noncardiac Surgery. Anesth. Analg. 2021, 132, 1654–1665. [Google Scholar] [CrossRef]
  36. Ahuja, S.; Mascha, E.J.; Yang, D.; Maheshwari, K.; Cohen, B.; Khanna, A.K.; Ruetzler, K.; Turan, A.; Sessler, D.I. Associations of Intraoperative Radial Arterial Systolic, Diastolic, Mean, and Pulse Pressures with Myocardial and Acute Kidney Injury after Noncardiac Surgery: A Retrospective Cohort Analysis. Anesthesiology 2020, 132, 291–306. [Google Scholar] [CrossRef]
  37. Li, W.; Hu, Z.; Yuan, Y.; Liu, J.; Li, K. Effect of hypotension prediction index in the prevention of intraoperative hypotension during noncardiac surgery: A systematic review. J. Clin. Anesth. 2022, 83, 110981. [Google Scholar] [CrossRef]
  38. Weinberg, L.; Li, S.Y.; Louis, M.; Karp, J.; Poci, N.; Carp, B.S.; Miles, L.F.; Tully, P.; Hahn, R.; Karalapillai, D.; et al. Reported definitions of intraoperative hypotension in adults undergoing non-cardiac surgery under general anaesthesia: A review. BMC Anesthesiol. 2022, 22, 69. [Google Scholar] [CrossRef]
  39. Sessler, D.I.; Khan, M.Z.; Maheshwari, K.; Liu, L.; Adegboye, J.; Saugel, B.; Mascha, E.J. Blood Pressure Management by Anesthesia Professionals: Evaluating Clinician Skill from Electronic Medical Records. Anesth. Analg. 2021, 132, 946–956. [Google Scholar] [CrossRef]
  40. Vernooij, L.M.; van Klei, W.A.; Moons, K.G.; Takada, T.; van Waes, J.; Damen, J.A. The comparative and added prognostic value of biomarkers to the Revised Cardiac Risk Index for preoperative prediction of major adverse cardiac events and all-cause mortality in patients who undergo noncardiac surgery. Cochrane Database Syst. Rev. 2021, 12, CD013139. [Google Scholar] [PubMed]
  41. Duma, A.; Maleczek, M.; Wagner, C.; Haslacher, H.; Szekeres, T.; Jaffe, A.S.; Nagele, P. NT-proBNP in young healthy adults undergoing non-cardiac surgery. Clin. Biochem. 2021, 96, 38–42. [Google Scholar] [CrossRef] [PubMed]
  42. Miller, W.L. Fluid Volume Homeostasis in Heart Failure: A Tale of 2 Circulations. J. Am. Heart Assoc. 2022, 11, e026668. [Google Scholar] [CrossRef] [PubMed]
  43. Strandgaard, S.; Paulson, O.B. Cerebral blood flow and its pathophysiology in hypertension. Am. J. Hypertens. 1989, 2 Pt 1, 486–492. [Google Scholar] [CrossRef] [PubMed]
  44. Burke, M.; Pabbidi, M.R.; Farley, J.; Roman, R.J. Molecular mechanisms of renal blood flow autoregulation. Curr. Vasc. Pharmacol. 2014, 12, 845–858. [Google Scholar] [CrossRef] [PubMed]
  45. Goodwill, A.G.; Dick, G.M.; Kiel, A.M.; Tune, J.D. Regulation of Coronary Blood Flow. Compr. Physiol. 2017, 7, 321–382. [Google Scholar] [CrossRef] [PubMed]
Figure 1. (A) shows an Acumen IQ minimally invasive sensor connected through radial artery line. (B) is an example secondary screen of derived hemodynamic parameters with HPI technology. In this example, with an HPI above 85, SVV at 14%, and Eadyn at 1.1, administering fluid therapy is the suggested response to prevent hypotension.
Figure 1. (A) shows an Acumen IQ minimally invasive sensor connected through radial artery line. (B) is an example secondary screen of derived hemodynamic parameters with HPI technology. In this example, with an HPI above 85, SVV at 14%, and Eadyn at 1.1, administering fluid therapy is the suggested response to prevent hypotension.
Jpm 14 00211 g001
Figure 2. Preoperative and postoperative troponin levels. Boxplots illustrate the median and interquartile range (IQR) of troponin concentrations at baseline and 24 and 48 h after surgery. The whiskers extend to the furthest points within 1.5 times the IQR from the upper and lower quartiles, as per Tukey’s method. The asterisk (*) denotes outliers.
Figure 2. Preoperative and postoperative troponin levels. Boxplots illustrate the median and interquartile range (IQR) of troponin concentrations at baseline and 24 and 48 h after surgery. The whiskers extend to the furthest points within 1.5 times the IQR from the upper and lower quartiles, as per Tukey’s method. The asterisk (*) denotes outliers.
Jpm 14 00211 g002
Figure 3. Preoperative and postoperative NtproBNP levels stratified by postoperative acute kidney injury. Boxplots illustrate the median and interquartile range (IQR) of NTproBNP levels at baseline and 24 and 48 h after surgery. The whiskers extend to the furthest points within 1.5 times the IQR from the upper and lower quartiles, as per Tukey’s method. The asterisk (*) denotes outliers.
Figure 3. Preoperative and postoperative NtproBNP levels stratified by postoperative acute kidney injury. Boxplots illustrate the median and interquartile range (IQR) of NTproBNP levels at baseline and 24 and 48 h after surgery. The whiskers extend to the furthest points within 1.5 times the IQR from the upper and lower quartiles, as per Tukey’s method. The asterisk (*) denotes outliers.
Jpm 14 00211 g003
Table 1. Patients’ Characteristics.
Table 1. Patients’ Characteristics.
VariableResult
Gender
Female, n (%)14 (30.4%)
Male, n (%)32 (69.6%)
Age, Years, Mean (SD), (Min–Max)69.83 (11.61), (36–86)
Chronic Diseases
Hypertension, n (%)32 (69.6%)
Coronary Heart Disease, n (%)16 (34.8%)
Chronic Obstructive Pulmonary Disease, n (%)1 (2.2%)
Asthma, n (%)3 (6.5%)
Diabetes, n (%)15 (32.6%)
Atherosclerosis, n (%)19 (41.3%)
Obesity, n (%)15 (32.6%)
Chronic Heart Failure, n (%) 21 (45.7%)
Chronic Kidney Disease, n (%)10 (21.7%)
ASA Score
3, n (%)30 (65.2%)
4, n (%)16 (34.8%)
Preoperative Oncological Treatment
Chemotherapy, n (%)25 (54.3%)
Radiotherapy, n (%)6 (13.0%)
Surgery Type
Right Hemicolectomy, n (%)9 (19.6%)
Left Hemicolectomy, n (%)3 (6.5%)
Anterior Resection of Rectum, n (%)7 (15.2%)
Gastrectomy, n (%)20 (43.5%)
Whipple Operation, n (%)6 (13.0%)
Cardia Resection, n (%)1 (2.2%)
Surgery Duration, Minutes, Mean (SD), (Min−Max)241.93 (97.10), (55–485)
Surgery Duration Interval
<2 h, n (%)4 (8.7%)
2–4 h, n (%)19 (41.3%)
>4 h, n (%)23 (50.0%)
Type
Open, n (%)29 (63.0%)
Laparoscopic, n (%)17 (37.0%)
POSSUM Score
Physiological Risk, Mean (SD), (Min−Max)26.76 (8.55), (14–54)
Surgical Risk, Mean (SD), (Min−Max)17.17 (5.55), (8–33)
Morbidity, %, Mean (SD), (Min−Max)75.66 (21.79), (23.33–99.69)
Mortality, %, Mean (SD), (Min−Max)34.58 (23.78), (4.07–92.69)
Total Hospitalization Time, Days, Mean (SD), (Min−Max)18.74 (11.48), (6–58)
Postoperative Hospitalization Time, Days, Mean (SD), (Min−Max)12.96 (9.02), (4–51)
Intraoperative Use of Inotropes or Vasopressors
Noradrenaline, n (%)45 (97.8%)
Dobutamine, n (%)17 (37.0%)
Combined use of
Noradrenaline and Dobutamine, n (%)17 (37.0%)
Baseline NTproBNP Level, pg/mL, Mean (SD), (Min−Max)641.33 (1994.89), (12.3–13,350.4)
Baseline Troponin Level, μg/L, Mean (SD), (Min−Max)0.0158 (0.01), (0.003–0.052)
Baseline Creatinine Level, mg/dl, Mean (SD), (Min−Max)1.05 (0.57), (0.61–4.49)
Abbreviations: SD—standard deviation, Min–Max—minimum and maximum values for a given parameter, ASA—American Society of Anesthesiologists scale, POSSUM—The Physiological and Operating Severity Scale for Mortality and Morbidity.
Table 2. Comparison of Hypotension Parameters in Patients with and without Intraoperative Hypotension Episodes.
Table 2. Comparison of Hypotension Parameters in Patients with and without Intraoperative Hypotension Episodes.
All Patients (n = 46)Patients without Hypotension Episodes (n = 8)Patients with Minimum of One Hypotension Episode (n = 38)
VariableMedianIQRMedianIQRMedianIQRp-Value
Total duration of monitoring (min)262.5147.8225164.5271.5123.80.434
Number of episodes with HPI > 859.51183.2511120.12
The number of hypotension episodes22.250023.25<0.001
Total duration of hypotension episodes, minutes36.50059.03<0.001
The proportion of time spent in hypotension, %1.313.18001.673.66<0.001
Average duration of each hypotension episode, min1.951.870021.44<0.001
Mean MAP if < 65 mmHg60.073.090060.073.09<0.001
AUT < 65 mmHg23.6753.920030.1753.25<0.001
TWA MAP < 65 mmHg0.08500.183000.120.25<0.001
Number of episodes with MAP < 50 mmHg0000000.194
Abbreviations: MAP—Mean Arterial Pressure; HPI—Hypotension Prediction Index (HPI) Value; AUT—Area Under the Threshold; TWA—Time-Weighted Average; IQR—Interquartile Range.
Table 3. Impact of Preoperative chronic heart failure and postoperative complications on intraoperative hypotension Parameters.
Table 3. Impact of Preoperative chronic heart failure and postoperative complications on intraoperative hypotension Parameters.
PreoperativePostoperative
HFAKIPMI
No (n = 25)Yes (n = 21) No (n = 35)Yes (n = 11) No (n = 41)Yes (n = 5)
VariableMdnIQRMdnIQRp-ValueMdnIQRMdnIQRp-ValueMdnIQRMdnIQRp-Value
Min 1 episode of hypotension, n (%)18 (72%) 20 (95%) 0.05528 (80%) 10 (91%) 0.65835 (85%) 3 (60%) 0.203
Total duration of monitoring (min)279120.17250177.50.2252791372301340.067259126.5357169.50.298
Number of episodes with HPI > 859911120.3471096140.4091011.58100.873
The number of hypotension episodes24220.37422160.84422.5270.914
Total duration of hypotension episodes, min39.8534.50.564362120.80636.5335.350.696
The proportion of time spent in hypotension, %1.033.111.43.50.321.213.21.45.530.3531.353.120.8410.010.764
Average duration of each hypotension episode, min22.921.891.920.6421.891.8323.350.33221.831.53.90.376
Mean MAP if < 65 mmHg60.074.0760.322.880.48360.192.2858.626.240.23360.142.9559.04−56.030.607
AUT < 65 mmHg22.6761.8424.6768.340.67421.6744.6728102.340.36624.6755.1711.33323.170.559
TWA MAP < 65 mmHg0.070.20.10.290.4260.070.170.110.750.250.090.170.030.910.645
Number of episodes with MAP < 50 mmHg00000.91600010.0270001.50.672
Abbreviations: MAP—Mean Arterial Pressure; HPI—Hypotension Prediction Index (HPI) Value; AUT—Area Under the Threshold; TWA—Time-Weighted Average; Mdn—Median; IQR—Interquartile Range; PMI—Perioperative Myocardial Injury; AKI—Acute Kidney Injury; HF—Preoperative Heart Failure.
Table 4. Perioperative NTproBNP Level Dynamics in Patients with and without Chronic Heart Failure.
Table 4. Perioperative NTproBNP Level Dynamics in Patients with and without Chronic Heart Failure.
All PatientsHeart FailureNo Heart Failure
N = 21N = 25
MdnIQRMin.Max.MdnIQRMdnIQRZp-Valuer
NT-pro-BNP–baseline183.9428.112.313,350.4435.9711.1587232.2−3.34<0.0010.49
NT-pro-BNP–24 h285.8679.839.010,558.5482.31067.6201.4268.1−3.080.0020.45
NT-pro-BNP–48 h276.7609.419.217,067.93461180.2157.6377.05−2.720.0060.4
Δ NT-pro-BNP–1-091.2177.4−2791.91959.7104.6292.770.9150.4−0.690.4870.1
Δ NT-pro-BNP–2-064.6241.0−4743.614,793.890.1290.3537192.6−0.450.6510.07
Δ NT-pro-BNP–2-1−31.3160.1−1951.713,034.8−60.6325.55−19.8110.3−0.690.4870.1
%Δ NT-pro-BNP–1-0177.6171.864.1658.8146.28117225.17267.82−2.150.0320.32
%Δ NT-pro-BNP–2-0166.0190.728.5793.2153.1145.86226.99269.58−1.160.2470.17
%Δ NT-pro-BNP–2-182.752.617.5658.581.5280.7483.8556.66−0.390.70.06
Abbreviations: NT-pro-BNP–baseline—preoperative Nt-pro-BNP serum concentration; NT-pro-BNP–24 h—Nt-pro-BNP serum concentration 24 h after the surgery; NT-pro-BNP–48 h—Nt-pro-BNP serum concentration 48 h after the surgery; Δ NT-pro-BNP–1-0—Difference in NT-proBNP concentration between the first postoperative day (NT-pro-BNP–24 h) and the preoperative Nt-pro-BNP measurement; Δ NT-pro-BNP–2-0—Difference in NT-proBNP concentration between the second postoperative day (NT-pro-BNP–48 h) and the preoperative Nt-pro-BNP measurement; %Δ NT-pro-BNP–1-0—Percentage change in NT-proBNP concentration between the first postoperative day (NT-pro-BNP–24 h) and the preoperative Nt-pro-BNP measurement; %Δ NT-pro-BNP–2-0—Percentage change in NT-proBNP concentration between the second postoperative day (NT-pro-BNP–48 h) and the preoperative Nt-pro-BNP measurement; %Δ NT-pro-BNP–2-1—Percentage change in NT-proBNP concentration between the second postoperative day (NT-pro-BNP–48 h) and the first postoperative day (NT-pro-BNP–24 h); IQR—interquartile range; Min.—minimum value; Max.—maximum value.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Cylwik, J.; Celińska-Spodar, M.; Dudzic, M. Individualized Perioperative Hemodynamic Management Using Hypotension Prediction Index Software and the Dynamics of Troponin and NTproBNP Concentration Changes in Patients Undergoing Oncological Abdominal Surgery. J. Pers. Med. 2024, 14, 211. https://0-doi-org.brum.beds.ac.uk/10.3390/jpm14020211

AMA Style

Cylwik J, Celińska-Spodar M, Dudzic M. Individualized Perioperative Hemodynamic Management Using Hypotension Prediction Index Software and the Dynamics of Troponin and NTproBNP Concentration Changes in Patients Undergoing Oncological Abdominal Surgery. Journal of Personalized Medicine. 2024; 14(2):211. https://0-doi-org.brum.beds.ac.uk/10.3390/jpm14020211

Chicago/Turabian Style

Cylwik, Jolanta, Małgorzata Celińska-Spodar, and Mariusz Dudzic. 2024. "Individualized Perioperative Hemodynamic Management Using Hypotension Prediction Index Software and the Dynamics of Troponin and NTproBNP Concentration Changes in Patients Undergoing Oncological Abdominal Surgery" Journal of Personalized Medicine 14, no. 2: 211. https://0-doi-org.brum.beds.ac.uk/10.3390/jpm14020211

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop