Methods: Between January 2019 and March 2019, a total of 204 patients (166 males, 38 females; mean age: 60.5±0.7 years; range, 59.2 to 61.9 years) who underwent isolated coronary artery bypass grafting and were monitored at least for 24 h in the intensive care unit postoperatively were included. Pre-, intra-, and postoperative data were recorded. The CASUS and APACHE II scores were calculated using the most abnormal values for each variable during the first 24 h, postoperatively. Clinical outcomes were seven-day mortality and 30-day mortality, need for reintubation, readmission to the intensive care unit, length of intensive care unit stay and length of hospital stay.
Results: The 30-day overall mortality was 4.9% (n=10). The CASUS scores were significantly higher for patients developing mortality within 30 days postoperatively (p=0.030) and for patients needing reintubation (p=0.003). In the receiver operating characteristic curve analysis predicting seven-day mortality and prolonged intensive care unit stay, the area under curve was higher for CASUS scoring compared to APACHE II (0.90 vs. 0.72 and 0.82 vs. 0.76).
Conclusion: The CASUS may prove to be a more reliable scoring system than APACHE II for predicting mortality and morbidity in patients undergoing isolated coronary artery bypass grafting.
Cardiac Surgery Score (CASUS) is a prognostic scoring system developed for cardiac surgery patients (Table 1). It is a simple model in which a failure of six organ systems is scored, which allows to gain total number of these points (Additive CASUS).
Table 1. Additive Cardiac Surgery Score (CASUS)
In the present study, we aimed to compare the reliability of Additive CASUS and APACHE II in predicting mortality and morbidity in patients undergoing isolated coronary artery bypass grafting (CABG).
Both preoperative data including age, sex, body mass index, comorbidities, ejection fraction (EF), the European System for Cardiac Operative Risk (EuroSCORE) values and the durations of both CPB and cross-clamp were recorded. Additive CASUS and APACHE II score were calculated for each patient using the most abnormal values within the first 24 h postoperatively. To avoid possible inconsistencies and missing data, all data were collected by a single physician and were checked periodically by the physician attending ICU.
Clinical outcomes were determined as postoperative morbidity and mortality. Mortality was defined as early mortality within postoperative seven days and late mortality within postoperative 30 days, in-hospital or out-of-hospital. Morbidity indicators were described as the length of both ICU and hospital stay, reintubation, ICU readmission, and prolonged postoperative ICU stay >48 h.
Patients who died intraoperatively or in the first postoperative 24 h were excluded. We evaluated only the first postoperative ICU admission among patients who were re-admitted to the ICU. Postoperative IABP, VAD, renal replacement therapy (RRT), extracorporeal membrane oxygenation (ECMO) support, cardiac arrest, revision surgery and other complications were recorded.
Statistical analysis
Statistical analysis was performed using the
SPSS version 21.0 software (IBM Corp., Armonk,
NY, USA). Continuous data were expressed in
mean ± standard deviation (SD), while categorical
variables were expressed in median and interquartile
range (IQR) or number and frequency. The Student
t-test was used for normally distributed numerical
variables comparing survivors and non-survivors.
The Mann-Whitney U test for non-normally
distributed numerical variables and chi-square test for categorical variables were used. Univariate
logistic regression analyses were performed
including independent variables regarding 30-day
and seven-day mortality as a dependent variable.
Multivariate logistic regression analyses were carried
out to identify statistically significant risk factors.
Receiver operating characteristic (ROC) analyses
were performed with the results of three scoring
systems regarding the postoperative 30-day and
seven-day mortality. The discrimination power of the
area under the curve (AUC) of <0.70 was considered
insignificant, 0.70-0.79 acceptable, 0.80-0.89 good,
?0.90 superior. A p value of <0.05 was considered
statistically significant.
Table 2. Comparison of data between survivors and non-survivors
The mean duration was 107.2±2.5 min for CPB and 66.4±2.0 min for cross-clamp, and there was no significant difference in CPB and cross-clamp times between survivors and non-survivors (p=0.289 and p=0.363, respectively).
The mean duration was 45.5±4.9 h for ICU stay and 213.9±11.1 h for hospital stay. Of 204 patients, 191 (93.6%) patients were extubated within the first 24 h postoperatively: 17 (8.3%) patients were reintubated and 20 (9.8%) patients needed readmission to the ICU. Among the patients who died within 30 days postoperatively, the rate of extubation at 24 h postoperatively was significantly lower (p=0.002), duration of ICU stay was significantly longer (p=0.028), rates of reintubation and readmission to the ICU, as well as CASUS scores were significantly higher (p=0.0001, p=0.0001 and p=0.03, respectively). Rates of revision surgery, cardiac arrest, IABP implantation and RRT were significantly higher in patients who died within postoperative 30 days (p=0.002, p=0.0001, p=0.001 and p=0.0001, respectively).
The odds ratios of CASUS and APACHE II were significant regarding seven-day and 30-day mortality (1.36 vs. 1.26 and 1.23 vs. 1.17) in the univariate logistic regression analysis (Table 3). The odds ratio of CASUS was observed higher regarding both seven-day and 30-day mortality than that of APACHE II. In the ROC analysis, the highest AUC (0.700) was found in the CASUS for 30-day mortality (Table 4 and Figure 1), the highest AUC (0.909) in the CASUS for seven-day mortality (Table 4 and Figure 2).
To predict mortality more precisely, we also performed multivariate analyses using CASUS and the parameters that were found significant in the univariate logistic regression analyses, including EF, APACHE II, and CPB time (Table 5). When CASUS, APACHE II, EF and CPB time were evaluated combined, the correct classification rate was up to 96.1%. The Hosmer- Lemeshow test results yielded a p value of 0.018, which showed that there was a significant difference between predicted and observed results.
Table 5. The multivariate logistic regression analysis in terms of 30-day mortality
The association of scoring systems with morbidity was evaluated considering reintubation, length of stay in the ICU and readmission to the ICU (Table 6). The CASUS score was significantly higher in patients requiring reintubation (p=0.003). The CASUS and APACHE II scores at postoperative 24 h were significantly higher in patients staying in the ICU >48 h (p=0.001 and p=0.001, respectively). In the ROC analysis of ICU stay, AUC was 0.828 for CASUS and 0.767 for APACHE II (Figure 3).
Table 6. Comparison of scoring systems in terms of predicting morbidity
Scoring systems common in ICUs were designed regardless of cardiac surgery patients; however, the reliability of APACHE II and SOFA for cardiac surgery patients has been proven.[2,3] The use of APACHE II and EuroSCORE were moderately beneficial to predict mortality after cardiac surgery.[2] A retrospective study involving 40 patients by Kartufan and Karaoğlu[3] reported that SOFA scores on the first postoperative day were significant and discriminated well to predict mortality (from 60 days to 1 year) after cardiac surgery. However, there are studies reporting that scores, including APACHE II, SOFA, the Simplified Acute Physiology Score (SAPS) II, Multiple Organ Dysfunction Score (MODS) were less accurate than CASUS.[4-7] Doerr et al.[4] reported that, of four scoring systems (CASUS, APACHE II, SAPS II and SOFA), CASUS and SOFA were reliable in predicting the mortality risk; and CASUS had the best discrimination among patients undergoing cardiac surgery. Exarchopoulos et al.[5] compared EuroSCORE II, CASUS, APACHE II, SAPS II and SOFA at the postoperative 24 h in predicting 30-day mortality and morbidity among cardiac surgery patients and found that CASUS had the best calibration and discrimination. Hekmat et al.[6] compared CASUS, APACHE II and MODS at postoperative 0 to five days after cardiac surgery in predicting mortality and reported that CASUS had a good calibration and the best discrimination for each day. Badreldin et al.[7] reported that CASUS and SOFA were reliable in predicting mortality among cardiac surgery patients and that CASUS predicted mortality more accurately. Badreldin et al.[8] in another study, identified that CASUS was eligible for daily scoring and could be used up to the sixth postoperative day. This study showed, consistent with previous studies, CASUS had very good discrimination regarding seven-day mortality, while the APACHE II did not. Our study may contribute to the utilization of additive CASUS more commonly in daily practice.
Logistic CASUS (logCASUS) was established integrating the number of ICU days into additive CASUS, which improved the prediction of mortality.[9] However, the calibration of the logCASUS was poor and the predicted and observed mortality were more consistent after recalibration.[10-12] In a comprehensive retrospective study by Wilson et al.,[10] logCASUS was shown to overpredict mortality after cardiac surgery and the expected and observed mortality were comparable after recalibration. However, Singh et al.[11] reported in their retrospective study with 7,098 patients that logCASUS underpredicted mortality compared with additive CASUS after cardiac surgery. The Rapid Clinical Evaluation (RACE), logCASUS and SOFA had good discrimination but poor calibration in predicting mortality after cardiac surgery. The logCASUS and RACE performed better after recalibration.[12] Changing treatment approaches and improvement in patient care may have highlighted need for recalibration. We used additive CASUS due to short ICU stay. Both additive CASUS and logCASUS predicted 30-day mortality well, and they had good discrimination.[11]
In the present cross-sectional study, the rate of mortality was higher than the expected rate, as was the need for IABP. While including patients in the study, we did not take account of preoperative EF values of patients. The non-survivors included in the study had significantly low preoperative EF, which may result in high mortality rates. In our study, age was found not to be a predictor for mortality, despite being a risk factor for open heart surgery. This was a finding consistent with the study conducted during the development of CASUS and that was likely to be related to the criteria for patient selection for surgery.[1] In the current study, preoperative EF was a predictor of mortality, while the duration of CPB was not. Madhavan et al.[13] examined patients undergoing isolated CABG, and reported that the total duration of CPB longer than 180 min was associated with increased postoperative complications. The duration of CPB was not a predictor for mortality in our study. It may be explained by the average duration of CPB <180 min.
Based on our study results, the EuroSCORE was not reliable in predicting 30-day mortality, which can be explained by the fact that parameters evaluating intraoperative and postoperative events are not included in EuroSCORE and the EuroSCORE consists of only the preoperative parameters. With experience gained over the years when logistic models were used, the EuroSCORE was updated as EuroSCORE II due to its overestimation of mortality.
Long-term ICU stay is associated with both operative and postoperative complications and it is also a predictor of morbidity and mortality. However, the definition of prolonged ICU stay after cardiac surgery is controversial, varying from 24 h to 14 days after ICU admission.[9] This study described prolonged postoperative ICU stay as longer than 48 h. The CASUS and APACHE II in the first 24 h postoperatively were significantly higher in patients with ICU stay longer than 48 h. In the ROC analysis regarding prolonged ICU stay, the CASUS showed a good discrimination, while APACHE II showed an acceptable discrimination. According to the current study, the CASUS can be used to predict prolonged ICU stay as it was previously reported.[5]
The CASUS, Intensive Care National Audit and Research Centre Score (ICNARC), APACHE II, and logistic EuroSCORE were compared and the CASUS was the best predictor of 30-day mortality. The ICNARC was superior to CASUS in predicting renal and pulmonary complications.[14] As compared with CASUS, ICNARC uses further data including age, a history of cardiopulmonary resuscitation before admission, cause of admission, urgent admission, as well as physiological parameters. The CASUS can more accurately predict mortality than other scoring systems. Using more data does not mean the prediction of mortality is more accurate. Moreover, optimal variables should be straightforward, repeatable and readily available. CASUS, comprising 10 variables, is more easily performed than the APACHE II and ICNARC.
Comparing CASUS and EuroSCORE, CASUS at 24 h postoperatively was not significant in predicting 30 day-mortality, despite its scores being higher in nonsurvivors.[15] This r esult may be related to the small sample size and the heterogeneity of the patient group.
The original study and most validation studies on CASUS were conducted in Germany. External validation studies were conducted long after the original study, being limited in numbers. Therefore, validation studies are required in diverse populations. Nonetheless, clinicians may benefit from CASUS in many ways in which they are able to explain the severity of the disease to patients and to their caregivers by predicting the mortality and morbidity more accurately as well as constructing a treatment plan. The CASUS can also be benefited to standardize research, to compare treatment modalities, to evaluate quality of care in the ICUs and to compare ICUs with each other, to provide proper use of ICU resources. Moreover, it is a practical evaluation method taking a few minutes in daily routine.
As the study was performed in a single center with small sample size, its results cannot be generalized. The CASUS and APACHE II were scored only for the first postoperative 24 h. Short ICU stay made it impossible to collect and evaluate data on the second and following days postoperatively.
In conclusion, the CASUS is more reliable than APACHE II in predicting mortality and morbidity among patients undergoing isolated coronary artery bypass grafting. Developed specifically for cardiac surgery patients, CASUS performs better, substantiating our main hypothesis. To predict mortality more accurately, further comprehensive studies evaluating patients undergoing a variety of open hearth surgeries are required with increasing number of patients and centers. Additional studies can be performed using logistic scoring systems to predict mortality for prolonged intensive care unit stay. We believe that CASUS should be widely used to obtain robust data for prediction of mortality and postoperative complications in centers where cardiac surgery is performed.
Acknowledgments: We extremely thankful to Dr. Hadi SAĞIN for statistical analysis.
Ethics Committee Approval: Haydarpaşa Numune Training and Research Hospital Clinical Research Ethics Committee, İstanbul (Chairperson Prof Ç. Nuhoğlu) approved this study (Ethical Committee Number 2018/91) on 17 December, 2018. The study was conducted in accordance with the principles of the Declaration of Helsinki.
Patient Consent for Publication: As the current study required only collecting the data, the Hospital Clinical Research Ethics Committee confirmed that informed consent from the patients were not warranted.
Data Sharing Statement: The data that support the findings of this study are available from the corresponding author upon reasonable request.
Author Contributions: Idea/concept: N.Y., Design: N.Y., S.U., M.A.; Control/supervision: S.U., N.Y., M.A.; Data collection and/or processing: S.U.; Analysis and/or interpretation: S.U.; Literature review: S.U.; Writing the article: S.U.; Critical review: N.Y., S.U., M.A.
Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.
Funding: The authors received no financial support for the research and/or authorship of this article.
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