Methods: Between August 1st, 2020 and December 1st, 2021, a total of 528 pediatric patients (264 males, 264 females; median age: 4 months; range, 2 days to 24 months) who were followed in the pediatric cardiac intensive care unit after congenital heart surgery were retrospectively analyzed. Demographic and clinical characteristics of the patients including operation and intensive care data were obtained from the medical records. Patients included in the study were categorized into three groups as the group of patients who were extubated in the operating room (fast-track extubation), the group of patients who were extubated in the first 6 h of the operation (early extubation), the group of patients who were extubated after the postoperative 6 h or the group of patients who were not extubated or died (delayed extubation).
Results: Sixty-eight (12.9%) cases had fast-tract extubation, 124 (23.6%) cases had early extubation, and 335 (63.6%) cases had delayed extubation. The median age of the patients in the delayed extubation group was three months, which was significantly lower than those of the other groups (p<0.05). Reintubation rates were 1.5% in the fast-tract extubation group, 2.5% in early extubation group, and 9% in delayed extubation group (p<0.05). The median intensive care unit stay was 3, 5, and 10 days, respectively (p<0.05). Length of hospitalization was significantly higher in the delayed extubation group compared to the other groups (p<0.05). Neonatal age group, Risk Adjustment for Congenital Heart Surgery 1 score >4, Society of Thoracic Surgeons- European Association for Cardio-Thoracic Surgery mortality category >3, cardiopulmonary bypass time >100/min, vasoactive inotrope score >8, acute kidney injury >2, and low weight were found to be independent risk factors for delayed extubation.
Conclusion: Fast-track and early extubation can be successfully applied with low reintubation rates in selected cases with congenital heart surgery. Age, body weight, presence of genetic syndrome, operational risk category, and procedure time may affect the extubation time.
The main goal of anesthesia in patients planning for surgery for CHDs is to provide hemodynamic stability, reduce mortality and morbidity, use resources economically, and prevent harm to the patient. Fulfilling these conditions is essential to tailor an anesthesia management strategy for CHD.[4]
Traditionally, patients were followed in the intensive care unit (ICU) with mechanical ventilator support after cardiac surgery. Recently, there has been an increase in the frequency of early extubation (EE) to avoid the adverse effects of positive pressure ventilation on the cardiovascular system, reduce airway irritation, and prevent complications such as ventilation-associated pneumonia. It has been advocated in different studies that factors such as age, body weight, the complexity of cardiac pathology, duration of operation, risk category, presence of syndrome, and anesthesia management are influential on extubation time. However, due to the adverse effects of cardiopulmonary bypass (CPB), the presence of immature organ systems, and sudden hemodynamic changes, when and where patients should be extubated is still a matter of debate.[5,6]
In the present study, we aimed to identify fast-track extubation (FTE), EE, and delayed extubation (DE) rates following a congenital heart operation and to evaluate the factors affecting FTE and DE.
A study form was created for each case. This form included preoperative data (demographic characteristics, preoperative clinical status, cardiac diagnosis, echocardiographic information, presence of syndrome, and redo status); operative data (presence of CPB, duration of operation, Risk Adjustment for Congenital Heart Surgery 1 [RACHS-1] score, and the Society of Thoracic Surgeons [STS]-European Association for Cardio-Thoracic Surgery (EACTS) mortality categories [STAT] score); and postoperative data (extubation time, length of stay in the ICU and hospital, mortality, highest vasoactive inotrope score [VIS, blood gas analysis, reintubation status, and complications). The RACHS-1, STAT, and VIS scores were calculated as reported in the literature.[7,8]
The cases included in the study were divided into three groups as the group of patients extubated in the operating room (FTE group), the group of patients extubated in the first 6 h after the operation in the ICU (EE group), and the group of patients extubated after the postoperative 6 h or the group of patients who were not extubated or died (DE group).[2]
The extubation decisions were taken by consensus between a pediatric cardiac intensivist with a five-year experience and a cardiac anesthesiologist. Extubation criteria were defined as staying awake without any stimulus, presence of spontaneous respiratory effort, a positive end-expiratory pressure (PEEP) 5 cmH2O, the fraction of inspired oxygen (FiO2) ≤0.4, oxygenation index (OI), arterial oxygen partial pressure (PaO2)/FiO2) >200, partial pressure of carbon dioxide (PaCO2) ≤50 mmHg, pH ≥7.25, a stable hemodynamic status, absence of systolic and diastolic dysfunction in echocardiography, and a good cough reflex and swallowing function. Extubation was postponed in case of delayed sternum closure, excessive bleeding, hemodynamic instability, and high-risk surgery.[4] Reintubation was defined as the need for mechanical ventilation after initial extubation attempt either in the operating room or in the ICU during the same hospital stay.[5]
All cases were planned to be extubated in the shortest time possible. In the perioperative anesthesia management, the appropriate medications were administered within the protocol framework used in the clinic where this study was conducted. Per protocol, in children aged six months, midazolam 0.1 mg/kg, fentanyl 1 µ ,g/kg, and rocuronium bromide 0.6 mg/kg were administered at induction; and remifentanil 0.1 µg/kg/min, rocuronium bromide 5 ?g/kg/min, and a minimum of 1 to 1.2 alveolar concentration sevoflurane were administered for maintenance. In children older than six months, midazolam 0.1 mg/kg, fentanyl 1 µg/kg, and rocuronium bromide 0.6 mg/kg were administered at induction; and remifentanil 0.25 µg/kg/min, rocuronium bromide 5 µg/kg/min, minimum of 1 to 1.2 alveolar concentration sevoflurane, and dexmedetomidine 0.5 µg/kg/h were administered for maintenance. The effects of neuromuscular agents were antagonized by sugammadex. Remifentanil and rocuronium were discontinued after the sternum was closed. Sevoflurane was discontinued before the skin was closed. Dexmedetomidine was continued, until the patient was transferred to the pediatric cardiac ICU.
The patients were initiated on milrinone 0.5 µg/kg/min at the beginning of the operation. The anesthesiologist decided the maintenance dose on a case-by-case basis, taking into consideration the initiation of catecholamine and the patient's hemodynamic status in the volume management during the operation.
Statistical analysis
Statistical analysis was performed using the IBM
SPSS version 22.0 software (IBM Corp., Armonk,
NY, USA). Descriptive data were expressed in median
(interquartile range [IQR]) and number and frequency,
where applicable. The Pearson chi-square test and
one-way analysis of variance (ANOVA) test were
used to compare the variables between groups. The
model developed for assessing the factors affecting
extubation featured the determination of independent
risk factors in the combined FTE and EE groups
based on the univariant analysis. Subsequently, the
factors which were determined to be independent risk
factors affecting extubation were analyzed using the
multivariate logistic regression analysis. The estimated
final model of the parameters predicting FTE or EE
was expressed in terms of odds ratio (OR) within
95% confidence interval (CI). A p value of <0.05 was
considered statistically significant.
Table 1. Main cardiac pathology results of the cases
The preoperative, intraoperative, and ICU data and univariant analysis results of the patients are summarized in Table 2.
Table 2. Preoperative, operative, and intensive care data
Preoperative data
The median age of the patients in the DE group
was significantly lower than those of the other
groups (p<0.05). The number of newborn cases was
significantly higher in the DE group (p<0.05). The
median bodyweight of the patients was 13 kg in the
FTE group, 6 kg in the EE group, and 3.2 kg in the DE
group (p<0.05). The presence of syndrome, presence
of pulmonary hypertension, and frequency of cyanotic
heart disease were all statistically significantly higher
in the DE group than the other two groups (p<0.05).
Operative data
Cardiopulmonary bypass was used in 84% of all
cases. The overall median CPB time was 75 (range,
60 to 95) min. The median CPB time in the FTE,
EE, and DE groups were 65 (range, 50 to 75), 77
(range, 60 to 100), and 105 (range, 80 to 125) min,
respectively, which was significantly higher in the
DE group compared to the other groups (p<0.001).
Similarly, the RACHS-1 scores and STAT mortality
categories were significantly higher in the DE group
than the FTE and EE groups (p<0.05).
Postoperative data
The overall reintubation rate was 6.4%. The
reintubation rates in the FTE, EE, and DE groups
were 1.5%, 2.5%, and 9%, respectively (p<0.05). Noninvasive
ventilation (NIV) rates in the FTE, EE, and
DE groups were 1.5%, 2.5%, and 3%, respectively. The
highest median blood gas lactate concentrations within
the first 24 h after surgery in the FTE, EE, and DE
groups were 4.1 (range, 2.8 to 6.1), 4.3 (range, 3.1 to 5.8),
and 5.2 (range, 4.2 to 7.5) mmol/L, respectively, and
did not significantly differ among the groups. The VIS
score, infection rate, and acute kidney injury (AKI) rate
were significantly higher in the DE group (p<0.05). No
significant difference was observed among the groups
regarding arrhythmia frequency (p>0.05). Median
lengths of stay in the ICU in the FTE, EE, and DE
groups were 3 (range, 2 to 4), 5 (range, 3 to 7), and 10
(range, 8 to 12) days, respectively, whereas the median
lengths of hospitalization in the FTE, EE, and DE
groups were 6 (range, 5 to 7), 7 (range, 5 to 10), and
13 (range, 10 to 21) days, respectively (p<0.05). There
was no mortality in the FTE group, whereas there
were three (2.4%) mortalities in the EE group and 34
(10.2%) mortalities in the DE group.
The factors with a p value of <0.05 as indicated by the univariate analysis from among the preoperative, operative, and ICU data were further analyzed using the multivariate regression analysis to identify the independent risk factors that caused DE. The independent risk factors are shown in Table 3. Accordingly, the RACHS-1 score >4 (OR: 3.7, 95% CI: 2.1-8, p=0.010), STAT level >3 (OR: 2.8, 95% CI: 0.9-7.4, p=0.004), AKI >2 (OR: 2.1, 95% CI: 1.4-6, p=0.007), neonatal age group (OR: 1.2, 95% CI: 0.7-1.5, p=0.02, CPB >100/min (OR: 4.4, 95% CI: 3.1-12, p=0.008), VIS >8 (OR: 2.7, 95% CI: 1.8-5.1, p=0.001) and low body weight during operation (OR: 0.8, 95% CI: 0.6-1.1, p=0.03) were identified as the independent risk factors.
Congenital heart diseases are a heterogeneous group which includes different anatomical and physiological features such as cyanotic/acyanotic, or single ventricle/double ventricle. In some studies, the primary cardiac diagnosis of the patients was associated with extubation. In one of these studies, Ödek et al.[9] reported that cases with atrial septal defect and ventricular septal defect were extubated earlier than those diagnosed with hypoplastic left heart syndrome and transposition of the great arteries. Similarly, it was reported in the case series of Tirotta et al.[2] that patients who were extubated early had different diagnoses, with atrial septal defect, ventricular septal defect, and tetralogy of Fallot being the most common. Likewise, in the current study, the most common EE cases had a diagnosis of atrial septal defect and ventricular septal defect or tetralogy of Fallot.
Early extubation rates reported in the literature vary significantly between 27 and 82%,[10,11] which can be attributed to different cut-off periods used to define EE. In some cases, EE is considered the extubation performed in the operating room, whereas in others, it is considered the extubation performed at 1 h, first 6 h, first 12 h, or first 24 h of the operation. A prospective study showed that 40% of the cases were extubated in the first 12 h, and 64% of the cases were extubated in the first 24 h of the operation.[9] Additionally, in a case series by Alam et al.,[12] 33.8% of the cases were extubated in the first 6 h of the operation. In comparison, in this study, 36.5% of the cases were extubated in the first 6 h of the operation.
The main reason for refraining from EE in congenital heart surgery is the frequent emergence of the need for reintubation. The reintubation rate reported in a multi-center pediatric cardiac intensive care study in newborns after cardiac surgery was 11% (range, 5 to 22%).[13] In another study, this rate was reported as 2.7% for all cases (1.5% in the operating room, 3.8% in the first 6 h, and 4% in the DE group), and there was no statistically significant difference between the EE and DE cases in terms of reintubation frequency.[2] In our study, the overall reintubation rate was 6.4%. The reintubation rates in the FTE, EE, and DE groups were 1.5%, 2.5%, and 9%, respectively (p<0.05). A higher reintubation rate in the DE group can be attributed to the fact that the patients in the DE group were younger and in the high-risk category.
In several studies, length of stay in the ICU and length of hospitalization have been related to EE.[14] Additionally, it has also been reported that the mortality rate varies between 0-5% in cases who are extubated early.[15,16] Similarly, in this study, the length of stay in the ICU and length of hospitalization were significantly lower in patients who were extubated early. Moreover, there was no mortality among the patients who were extubated early.
Many different preoperative, intraoperative, and postoperative factors may affect EE. In a study conducted by Wu et al.,[4] age, bodyweight at the time of operation, whether the lungs were pneumonic in the preoperative stage, type and duration of CPB, presence of deep hypothermic circulatory arrest, whether ultrafiltration was used, and STAT categories were found to be independent risk factors associated with EE. In the studies of Simeonov et al.,[14] malnutrition and extended CPB duration adversely affected extubation success. In a case series of Tirotta et al.[2] including 338 cases, low flow perfusion, presence of deep hypothermia, presence of red sternotomy, use of medications such as furosemide, epinephrine, and vasopressin, provision of cardiopulmonary support, history of pulmonary edema, presence of syndrome and difficult intubation were found to be significantly associated with DE. In our study, preoperative, operative, and postoperative risk factors that could affect DE were evaluated extensively. Consistent with the results of the aforementioned studies, factors such as being newborn, presence of syndrome, being in the highrisk category, long CPB time, and high VIS score were identified as independent risk factors causing DE.
The single-center, retrospective design with a relatively short-term results is the main limitation to this study. Further large-scale, prospective studies are needed to confirm these findings.
In conclusion, fast-track and early extubation can be successfully applied with low reintubation rates in selected cases with congenital heart surgery. Age more than 30 days, less complex procedures (RACSH-1 <4), absence of a genetic syndrome, shorter cardiopulmonary bypass time, and lower vasoactive inotrope score (<8) may predict fast-track and early extubation.
Ethics Committee Approval: The study protocol was approved by the University of Health Sciences, Başakşehir Çam and Sakura City Hospital Local Ethics (date: 29.12.2021, no: 300). The study was conducted in accordance with the principles of the Declaration of Helsinki.
Patient Consent for Publication: A written informed consent was obtained from the parents and/or legal guardians of the patient. 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, writing the article, references and fundings, materials: S.O., E.O.; Design, control/ supervision: S.O., H.D.O., E.O.; Data collection and/or processing, analysis and/or interpretation, literature review: S.O., H.D.O., E.O., S.S., İ.A.K., Z.B.T., O.Y.; Critical review: S.O., E.O., F.G.O., A.H.; Other: S.O.
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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