Introduction

Cardiovascular complications are encountered following surgical repair of aortic coarctation, despite apparently successful procedures [1,2,3,4,5,6]. Although many of the complications are related to anatomical problems such as restenosis and aneurysm formation, there are some complications that are not directly related to the morphological problems of the reconstructed aorta. One of the most important complications is the early onset of cardiovascular diseases, such as hypertension, myocardial infarction, cardiac failure, stroke, and sudden death [7,8,9]. Complications have been reported even in cases where aortic arch repair is completely successful. Cohen and colleagues have reported that the most important predictor of long-term survival and hypertension in patients was the age of patients at the time of the initial repair [4]. The report suggested that preoperative cardiovascular damage influences the postoperative condition. However, O’Sullivan and colleagues reported that patients suffered from hypertension after an early and successful aortic coarctation repair [9]. Many hypotheses have been proposed to explain these observations.

We have previously reported that the repaired site generates an extra pressure wave reflection, which might cause future cardiovascular disease [10]. The enhancement of the pressure wave reflection leads to an increase in left ventricular workload and is disadvantageous for coronary circulation. The damaged cardiac blood supply–workload balance could induce heart failure, arrhythmia, and sudden death. Therefore, we analyzed cardiac blood supply–workload balance in patients after aortic arch repair.

Methods

Patients (Table 1)

We enrolled 17 patients who had undergone aortic arch repair for a coarctation of the aorta or an interruption of the aortic arch without an aortic recoarctation. Aortic recoarctation was defined as an aorta with a structural stenosis or an existence of a systolic blood pressure (SBP) difference at the repaired site. No patients had any significant leakage at the aortic level, including patent ductus arteriosus and aortic regurgitation. The mean age of the patients was 6.8 ± 2.8 years (range 1–13 years). The patients underwent an aortic arch repair at 28.9 ± 29.0 days (range 3–103 days). The aortic arch repair was performed by an extended end-to-end anastomosis in 12 patients (70.6%), subclavian flap in 4 patients (23.5%), and a Blalock–Park operation in one patient (5.9%). Thirteen patients (76.5%) had a ventricular septal defect and underwent a closure of the defect at the mean age of 0.76 ± 0.49 years (range 0.17–2.0 years). The postoperative course was uneventful. Seven patients (41.2%) were diagnosed with a bicuspid aortic valve without aortic stenosis or aortic regurgitation. All patients were fully active and asymptomatic. None of the patients were on cardiovascular medications.

Table 1 Patients’ profile

Control 1-to-1, age-matched patients had small left-to-right shunt disorders (12 patients with ventricular septal defects and five with atrial septal defects) [11], because it has been reported that the value of a subendocardial viability ratio in children, which we used to evaluate cardiac blood supply–workload balance, depends on the patient’s age [12]. Their mean pulmonary-to-systemic flow ratio was 1.2 ± 0.2 (range 1.0–1.5). They were also asymptomatic and were given no medications. There were no differences in height (117.1 ± 21.3 cm), weight (25.2 ± 15.9 kg), or body surface area (0.88 ± 0.34 m2) compared with the patient test group (Table 1). There were no differences in cardiac index (4.1 ± 0.7 l/min m2) and heart rate (94.0 ± 17.0 bpm) between the control and test groups.

Parents of all subjects gave their informed consent. The study protocol was approved by the ethics committee of Chiba Children’s Hospital and Hokkaido University Hospital.

Data Acquisition

Ascending aortic pressure waveforms were recorded using a catheter-mounted pressure sensor (Millar, SPC-454D; Millar Instruments, Inc. Houston, TX) during cardiac catheterization for evaluation of postoperative hemodynamics. The ascending aortic pressure waveform was recorded at one vertebral body thickness above the aortic valve. Patients were sedated by a venous injection of midazolam during cardiac catheterization. The waveform was recorded on a hard disk through an analog–digital converter with a sampling rate of 1000 Hz (1000 samples per second). It was also simultaneously recorded with an electrocardiogram.

Data Analysis

From the recorded pressure waveforms, we measured the SBP, diastolic blood pressure (DBP), mean blood pressure (MBP), and pulse pressure (PP) in each patient. Moreover, we calculated a subendocardial viability ratio according to the following equation:

$$ {\text{Subendocardial}}\;{\text{viability}}\;{\text{ratio = diastolic}}\;{\text{pressure}}\;{\text{time}}\;{\text{index}} /{\text{tension}}\;{\text{time}}\;{\text{index}}. $$

The subendocardium is thought to be more sensitive to shortage of the blood supply than the subepicardium. Buckberg and colleagues demonstrated that the ratio of the diastolic phase area (diastolic pressure time index) to the area of the systolic phase (tension time index) in the central aortic pressure profile has a close correlation to the blood supply to the subendocardium. That ratio was designated as the subendocardial viability ratio [13,14,15] (Fig. 1).

Fig. 1
figure 1

Measurement of a subendocardial viability ratio

Therefore, they coined this index as a measure of the hemodynamic capacity for the supply divided by the myocardial oxygen demand. The tension time index was obtained by measuring the area under the aortic pressure curve in systole; it equaled the mean aortic pressure in systole multiplied by the duration of systole. The diastolic pressure time index was obtained by measuring the area under the aortic pressure curve in diastole and subtracting the mean left atrial pressure (assumed to be equal to the left ventricular diastolic pressure) multiplied by the diastolic time from it. When the left atrial pressure was not recorded, we used the pulmonary capillary wedge pressure instead.

Statistical Analysis

All values are reported as mean ± SD where applicable. We compared the difference in the hemodynamic data and subendocardial viability ratio values in patients after the aortic arch repair with those in the age-matched control subjects by a paired t test.

Results

Cardiac catheterization data are shown in Table 2. Blood pressure values were measured in the ascending aorta. The SBP was significantly higher (100.4 ± 12.9 vs. 90.2 ± 8.9 mmHg, p = 0.0011) and PP was significantly wider (38.1 ± 7.1 vs. 32.5 ± 5.4 mmHg, p = 0.0072) in patients after aortic arch repair compared with age-matched controls. Moreover, DBP (62.3 ± 9.8 vs. 57.7 ± 6.7 mmHg, p = 0.019) and MAP (80.2 ± 13.5 vs. 74.4 ± 7.3 mmHg, p = 0.049) were significantly higher in patients compared with the control subjects. Table 3 summarizes the subendocardial viability ratio data. Although there was no difference in the subendocardial viability ratio between the patients and control subjects (1.01 ± 0.25 vs. 1.01 ± 0.24, ns), the tension time index (27.4 ± 5.6 vs. 23.0 ± 3.3, p = 0.0001), which reflects the workload of the left ventricle, and the diastolic pressure time index (28.4 ± 11.1 vs. 23.6 ± 8.0, p = 0.0082), which reflects the blood supply to the subendocardium, were significantly higher in patients after aortic arch repair.

Table 2 Blood pressure data
Table 3 Subendocardial viability ratio

Discussion

The current study demonstrates that the subendocardial viability ratio, which is a measure of cardiac blood supply–workload balance, was not significantly affected following successful aortic arch repair. However, tension time index, which measures cardiac workload, and diastolic pressure time index, which measures coronary blood supply, both increased. Because the subendocardial viability ratio is a ratio of diastolic pressure time index to tension time index, the value was not significantly affected even though the two parameters increased.

We have previously reported on subendocardial viability ratio in patients after an arterial switch operation [16]. The results were almost identical to those described here, i.e., no significant difference in subendocardial viability ratio despite an increase in tension time index of the patients. Maintaining a cardiac blood supply–workload balance is essential for survival. Hence, it is important to maintain the subendocardial viability ratio and many reports have demonstrated the relationship between low subendocardial viability ratio and poor outcome [17,18,19,20,21].

Our results demonstrate that blood pressure parameters were higher in patients after aortic arch repair compared with controls. Previous studies have reported decreased distensibility of the proximal aorta [22,23,24,25,26] and hence left ventricular hypertrophy [24, 27, 28] in patients after aortic coarctation. We have previously reported that the degree of left ventricular hypertrophy is associated with the enhancement of pressure wave reflection in patients after aortic arch repair, and that the hypertrophy may lead to abnormal pathogenesis associated with myocardial fibrosis [28, 29].

Czernin and colleagues have previously reported that a gradual decline of myocardial blood flow reserve with aging correlates with an age-related increase of baseline myocardial work and blood flow [30]. Systolic blood pressure in aged subjects was higher than that in young subjects and may increase cardiac workload. This scenario resembles the one we describe in the current study where increased coronary blood flow is associated with augmented cardiac workload. Hauser and colleagues have reported decreased coronary flow reserve with the increase of resting basal coronary blood flow in patients after an arterial switch procedure [31]. This finding is in agreement with the study by Czernin and colleagues regarding coronary circulation and the aging process [30]. Therefore, cardiac blood supply–workload balance in young patients after aortic surgery may be similar to that in aged individuals, i.e., aortic function may be damaged in a way that is disproportionate with chronological age. Further studies are needed to elucidate the mechanism of cardiac blood supply–workload balance in patients after aortic arch repair.

One of the most important limitations of the current study is that the control subjects had a left-to-right shunt. Therefore, cardiac workload could be slightly overestimated. Judging from the product of their flow ratio and pulmonary artery pressure, the increment of the cardiac workload was under 5%. However, it could influence cardiac blood supply–workload balance. Because we recorded pressure waveforms in children by an invasive method, it was necessary to administer sedative drugs, which could influence cardiac blood supply–workload balance. Despite these limitations, the relationship between the parameters should be reliable in each condition.

Conclusion

Cardiac blood supply–workload balance is preserved in patients after aortic arch repair, despite an increase in cardiac workload.