Methods: We retrospectively reviewed the medical records of 29 children (16 males, 13 females; mean age 21.6 months; range 5 days to 162 months) who underwent open heart surgery and required extracorporeal membrane oxygenation support due to postcardiotomy circulatory failure between February 2010 and March 2015.
Results: The most common diagnosis was tetralogy of Fallot in eight patients (27.5%). The most common extracorporeal membrane oxygenation indication was failure to wean from cardiopulmonary bypass in 12 (41%) patients. The mean duration of extracorporeal membrane oxygenation support was 6.9 days (range 14 hours to 32 days). The most common complication related to extracorporeal membrane oxygenation support was renal insufficiency in 14 patients (48.3%). Fourteen patients (48%) were able to be successfully weaned from extracorporeal membrane oxygenation support, while six patients (20.7%) were discharged without any neurological sequelae. No significant predictor of mortality was found. Failure to wean from cardiopulmonary bypass resulted improved outcomes than other extracorporeal membrane oxygenation indications.
Conclusion: Extracorporeal membrane oxygenation provides an effective cardiopulmonary support for cardiopulmonary failure after pediatric open heart surgery. Careful patient selection, and correct timing and appropriate management of extracorporeal membrane oxygenation are crucial for optimal outcomes.
Although left ventricular failure is a common cause for ECMO support in adult patients, right ventricular failure, respiratory failure and pulmonary hypertension often contribute substantially, when mechanical circulatory support is required in pediatric cases. Many published reports of ECMO outcomes from several institutions have demonstrated considerable variability in survival rates, due to the differences in anatomic diagnosis, surgical procedures, ECMO indications, and management of ECMO.[1,4,5] Therefore, an appropriate ECMO support and management can be chosen individually for each case, based on their anatomy and surgical procedure.[6]
In the present study, we present our five-year ECMO experiences in patients requiring mechanical support after pediatric open heart surgery.
Venoarterial ECMO was used in all patients. Extracorporeal membrane oxygenation circuit consisted of a centrifugal pump, membrane oxygenator, heat exchanger, inlet and outlet cannulas, and circuit tubing. The cannulation sites were the ascending aorta for arterial inflow and right atrium for venous outflow. The ECMO circuit was established with the same cannulas (DLP, Medtronic, Inc., Minneapolis, MN, USA) used for cardiopulmonary bypass (CPB) in patients with intraoperative failure to wean from CPB. The MEDOS Deltastream II (MEDOS, Medizintechnik AG, Stolberg, Germany) ECMO system was used in all patients. In infants up to 15 kg of body weight, the Terumo Capiox FX05 (Terumo Cardiovascular Systems Corporation, Ann Arbor, MI, USA) oxygenator was used, while in children over 15 kg, the Terumo Capiox FX15 (Terumo Cardiovascular Systems Corporation, Ann Arbor, MI, USA) oxygenator was utilized. The ECMO circuit was primed with human albumin 20%, fresh frozen plasma, and sodium bicarbonate before its connection to the cannulas. After ECMO system was set, the flow rate was slowly increased up to 100 to 200 mL/min/kg according to age and body surface area of each patient, and additionally depending on hemodynamic stability, blood gas samples, serum lactate levels, urine output, and mixed venous oxygen saturation reflecting the effectivity of tissue perfusion. None of the patients were cooled during the ECMO support. The main goal was to provide a mean systemic oxygenated arterial blood flow of 2.4 L/min/m2 as a complete circulatory support.[7]
Anticoagulation was administered by heparin infusion, maintaining activated clotting time (ACT) ranging between 180 and 200 sec. Activated clotting time and arterial blood gas parameters were checked hourly. Mechanical ventilation was set to ECMO resting settings, which includes a respiratory rate of 8 to 12/min, tidal volume of 6 to 8 mL/kg with a positive end-expiratory pressure of 5 to 10 cmH2O, and 40% fraction of inspired oxygen (FiO2). All patients were paralyzed with neuromuscular blocking agents, and deeply sedated with benzodiazepine and narcotic analgesics. Inotropic drugs were continued in most patients to support cardiac functions and to prevent left ventricle distension. Blood product administration during ECMO was based on our institutional standard protocol for the management of ECMO patients including packed red blood cells to maintain hematocrit above 30% and platelets to maintain their count above 75,000/μL.
Echocardiography was performed once daily in all patients to evaluate cardiac functions and to determine if any potentially correctable cardiac defect was present. In case of hemodynamic stability, as evidenced by recovered ventricular function on echocardiography, normal blood pressure, lactate levels (≤2 mmol/L), and mixed venous saturation (≥65), weaning was attempted. Before weaning, ventilator support, fluid status, and inotropic support, and vasodilator treatment were optimized.
Weaning from ECMO was achieved by optimizing inotropic and ventilator support and gradually decreasing ECMO flow rates within 12 hours to minimum (approximately 100 mL/min). When flow rates decreased to approximately 25% of the maximal support, the bridge between the arterial and venous systems was opened, turning the stopcocks and allowing blood flow through the bridge from the arterial to venous side. The arterial and venous lines above the bridge were clamped to isolate the patient from ECMO, and the circuit was allowed to re-circulate. Once the patient was off complete support, hemodynamic stability was monitored, and tissue perfusion was assessed by arterial blood gases with serum lactate and base deficit values. Echocardiography was often used to evaluate myocardial function during the weaning process. After at least one hour of hemodynamic stability, cannulas were removed, and all purse-string sutures were left in place and re-snared. The chest was left open, and skin edges were sutured primarily.
Statistical analysis
Statistical analysis was performed using the PASW
version 18.0 software (SPSS Inc., Chicago, IL, USA). Continuous variables were expressed in mean ± standard
deviation and median (min-max), while categorical
variables were presented in frequency and percentage.
The normality test of all the variables was performed.
Continuous variables were compared by survival status
using the Student t-test, while categorical variables
were compared by survival status using the chi-square
or Fishers exact tests. Two-tailed p values of <0.05
were considered statistically significant.
The patients were also classified according to the risk adjustment for congenital heart disease based on the Risk Adjustment in Congenital Heart Surgery (RACHS-1) scores (Table 2).[8] The mean aortic cross-clamp time and CPB time during surgery were 74.1±21.6 min and 127.6±51.9 min, respectively. The mean duration of ECMO support was 6.9 days (range 14 hours to 32 days). Complications during ECMO included renal insufficiency requiring additional hemofiltration or dialysis in 14 (48%), bleeding from surgical and cannulation sites in nine (31%), liver insufficiency in six (21%), pulmonary edema in six (21%), tubing or pump head occlusion in three (10%), intracranial hemorrhage in two (7%), and gastrointestinal bleeding in one patient (3%). Fourteen patients (48.3%) were able to be successfully weaned from ECMO support. Six patients (20.7%) were discharged. None of the remaining survivors had any neurological sequelae at the time of discharge.
Table 2: Weaning and survival rates according to the RACHS-1 classification
Possible risk factors affecting mortality is shown in Table 3. Mortality was not associated with demographic characteristics of the patients. Interestingly, longer aortic cross-clamp time and CPB time during surgery did not result in a statistically poorer outcome. In addition, longer duration of ECMO support was not found to be associated with mortality. The laboratory tests at ECMO initiation such as arterial pH and lactate were not found to be associated with mortality, either. However, failure to wean from CPB resulted improved outcomes than other ECMO indications.
Currently, indications for use of ECMO in pediatric population have been expanded, including circulatory support before congenital cardiac surgery,[13] severe myocardial dysfunction and myocarditis as a bridge to recovery,[14,15] or as bridge to transplantation,[14-16] treatment of pulmonary hypertension,[17] circulatory support after congenital cardiac surgery,[1,2,10-12] and after transplantation.[18] Extracorporeal membrane oxygenation indications for postcardiotomy circulatory support in pediatric cardiac surgery cases are affected by many factors such as ventricular function, response to conventional inotropic support, and pulmonary artery pressure. Unfortunately, no universally accepted standardized indication criteria or management guidelines have been established for ECMO in congenital heart disease, due to its complex nature and specificity of use.[19] Therefore, many centers have constituted their own indication criteria and management protocols based on their experiences. In a recent study, the establishment of an ECMO program, creating a trained and experienced ECMO team, and multidisciplinary approach have been suggested to be critical to obtain good results.[20]
Many factors including baseline ECMO clinical
status, diagnosis, cardiac surgical procedures, timing
of initiation of ECMO and ECMO-related factors may
affect outcomes for postcardiotomy patients supported
with ECMO. The risk factors associated with mortality
in children who were supported with ECMO after
cardiac surgery were described by Morris et al.[21]
These risk factors were age below one month, male
gender, longer duration of mechanical ventilation
before support, and development of renal or hepatic
dysfunction while on support. However, functional
cardiac physiology (univentricular or biventricular),
ECMO indications, and duration of ECMO were
not found to be associated with an increased risk of
mortality. On the other hand, in a recent study, Gupta
et al.[
Furthermore, the timing of initiation of ECMO
before circulatory collapse is crucial to prevent endorgan
injuries, particularly neurological and renal
injuries. However, the optimal timing of initiation
of ECMO support is not well-defined, and it is often
institution-specific.[26] In a study conducted by Itoh
et al.,[
In several studies, survival rates of over 50% have
been reported after surgery.[1,10,13] In our series, the
weaning rate from ECMO was 48%, and the survival to
discharge rate without any neurological sequelae was
20%, which is relatively lower than previous reports
in the literature. This can be partly explained by the
relatively radical patient selection. In our institution,
ECMO use has been increasing for pediatric cardiac
surgery cases with postcardiotomy circulatory failure;
however, familiarity with this technique is relatively
new. In addition, considering the results of the past
two years, it seems that our survival rate has increased
from 20 to 30%, indicating that we still need to have
a learning curve period to obtain satisfactory results.
Of note, it should be kept in mind that the ECMO
protocol and ECMO team have been recently created
in our institution.
Complications related to ECMO decrease the
survival rates in all patients, and the incidence of
ECMO complications increases with prolonged ECMO
support. There are several complications which are
directly and indirectly related to ECMO circuit. The
common complications which are directly related to
the ECMO circuit include oxygenator degradation,
deterioration of the pump, and other circuit and
cannula-related problems. Indirect ones are bleeding
from the surgical site, cannulation-site, intracranial,
gastrointestinal areas, neurological events, renal
insufficiency, hemolysis, arrhythmia, pneumothorax,
and culture-confirmed infections at any site.[15,27]
To the best of our knowledge, our study is the
first including the largest case series of ECMO for pediatric cardiac surgery cases in Turkey. Nonetheless,
it has several limitations. First, as ECMO therapy is
relatively new in our institution, we have relatively a
small sample size. Second, the retrospective design of
the study is the inherent limitation of the potentially
inconsistent nature of data in the medical records.
Third, there was a significant difference in the number
of survivor and non-survivors, precluding statistically
significant analyses of the risk factors associated with
mortality.
In conclusion, extracorporeal membrane
oxygenation provides an effective cardiopulmonary
support for cardiopulmonary failure after open heart
surgery in pediatric cases. Careful patient selection,
and correct timing and appropriate management of
extracorporeal membrane oxygenation are of utmost
importance to achieve optimal outcomes. However,
further experiences, technological improvements, and
establishment of an ECMO program with experienced
ECMO team are required to obtain improved outcomes.
Declaration of conflicting interests
Funding
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
The authors received no financial support for the research
and/or authorship of this article.
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