Microvolt T wave alternans in adults with congenital heart diseases characterized by right ventricle pathology or single ventricle physiology: a case control study.

BACKGROUND: Among adults with congenital heart diseases (CHD) evaluation of sudden cardiac death (SCD) risk remains a great challenge. Although microvolt T-wave alternans has been incorporated into SCD risk stratification algorithm, its role in adults with CHD still requires investigation. We sought to determine the incidence of MTWA in this specific group and its coincidence with ventricular arrhythmia (VA) and other clinical findings presumably associated with SCD.
METHODS: A case-control study was performed in which 102 patients with CHD characterized by right ventricle pathology or single ventricle physiology (TGA, UVH, Ebstein's anomaly, ccTGA, Eisenmenger syndrome, DORV, CAT, unoperated ToF) were compared to 45 age- and sex-matched controls. All subjects underwent spectral MTWA test, ambulatory ecg monitoring, cardiopulmonary test, BNP assessment. After excluding technically inadequate traces, the remaining MTWA results were classified as positive(+), negative(-) and indeterminate(ind). Due to similar prognostic significance MTWA(+) and (ind) were combined into a common group labeled 'abnormal'.
RESULTS: Abnormal MTWA was present more often in the study group, compared to controls (39.2% vs 2.3%, p = 0.00001). Sustained ventricular tachycardia (sVT) was observed more often among subjects with abnormal MTWA compared to MTWA(-): 19.4% vs 3.6%, p = 0.026. The patients with abnormal MTWA had a lower blood saturation (p = 0.047), more often were males (p = 0.031), had higher NYHA class (p = 0.04), worse cardiopulmonary parameters: %PeakVO2 (p = 0.034), %HRmax (p = 0.003). Factors proven to increase probability of abnormal MTWA on multivariate linear regression analysis were: sVT (OR = 20.7, p = 0.037) and male gender (OR = 15.9, p = 0.001); on univariate analysis: male gender (OR = 2.7, p = 0.021), presence of VA (OR = 2.6, p = 0.049), NYHA > I (OR = 2.06, p = 0.033), %HRmax (OR = 0.94, p = 0.005), %PeakVO2 (OR = 0.97, p = 0.042), VE/VCO2slope (OR = 1.05, p = 0.037).
CONCLUSIONS: Abnormal MTWA occurs significantly more often in adults with the chosen forms of CHD than among healthy subjects. The probability of abnormal MTWA increases in patients with malignant VA, in males and among subjects with heart failure and cyanosis. MTWA might be of potential role in risk stratification for SCD in adults with CHD.

Background

A dynamic progress of pediatric cardiosurgery made survival to adulthood possible for most patients with congenital heart defects (CHD) [1-4]. Most die due to cardiovascular complications including a sudden cardiac death (SCD) that accounts for 19%-30% of total mortality and is observed mainly in patients with complex forms of CHD [1-6]. Majority, i.e. 75%-80%, of SCD is caused by ventricular fibrillation [5,6] but still this heterogenous population lacks fine indications for implantable cardioverter-defibrillator (ICD) therapy in primary prophylaxis [7]. Ventricular arrhythmia (VA) among these patients originates from myocardial fibrosis due to cyanosis and insufficient intraoperative cardioprotection; scars after ventriculotomy; hemodynamic changes resulting in ventricular dilation and increased wall stress, consequentially causing areas of electrical inhomogeneity within myocardium [2,8]. Noninvasive risk stratification for arrhythmic SCD is based on factors that possibly contribute to the aforementioned pathological chain that includes presence of malignant VA during ecg ambulatory monitoring [5,9], heart failure [10-12], or widening of QRS complex reflecting intra- and interventricular delay [9]. Nevertheless, such management still lacks accuracy.

Microvolt T wave alternans (MTWA) – an electrocardiographic phenomenon displaying inhomogeneity of the myocardial repolarization process is a promising method of VA risk evaluation in patients with ischemic and non-ischemic cardiomyopathies [13-15], which has been recently included into guidelines for the SCD prevention (class IIa) [6]. It has been proven that the heterogeneity of the intracardiac repolarization leads to dispersion of the depolarizing wave, reentry phenomenon and, as a consequence, initiation of the ventricular arrhythmia [6]. To our best knowledge, there have been merely two studies on spectral MTWA phenomenon in CHD patients published so far, both concerning only pediatric population [16,17]. Therefore, the aim of our study was to determine the incidence of spectral MTWA among grown-up patients with the chosen forms of CHD characterized by pathology within right ventricle or single ventricle physiology. Moreover, we evaluated the coincidence between MTWA and malignant and potentially malignant ventricular arrhythmia, as well as other demographic and clinical findings presumably associated with an increased risk of malignant VA and SCD in the analyzed population.

Methods

The study group consisted of 102 consecutive patients (47 males) in sinus rhythm diagnosed with CHD characterized by pathology within right ventricle or single ventricle physiology, aged 18-75 years (mean 34.2 ± 13.6 years), of whom 46 (45.1%) were operated on at the age of 0.5-32 years (mean 6.2 ± 6.3 years). None of them had indications for ICD in secondary prophylaxis. Five patients (4.9%) presented with common arterial trunk (CAT), 9(8.8%) – congenitally corrected transposition of the great arteries (ccTGA), 6(5.9%) – double outlet right ventricle (DORV), 32(31.4%) - Ebstein’s anomaly, 9(8.8%) – Eisenmenger syndrome due to simple shunt lesions, 20(19.6%) – complete transposition of the great arteries (TGA), 3(2.9%) – native tetralogy of Fallot (ToF), 18(17.7%) – univentricular heart (UVH) including 8 patients with tricuspid atresia, 3 – ccTGA, 4 – double inlet left ventricle (DILV) and 3 – common atrioventricular canal (CAVC). Surgical correction was performed in 2 (40%) patients with CAT, 6 (100%) with DORV, 2 (6.2%) with Ebstein anomaly, 18 (90%) with TGA (using method of intraatrial repair), 12 (66.6%) with UVH (including 11 Fontan operations and 1 pulmonary banding). The control group consisted of 45 healthy volunteers (23 males) aged 18-65 years (mean 31.0 ± 9.2 years). The exclusion criteria were: persistent atrial fibrillation, permanent cardiac pacing, serum creatinine > 140 μmol/l, serum aspartate transaminase level exceeding twice the upper limit of normal, pulmonary diseases, mental or physical disability preventing cooperation. Functional status was assessed according to the New York Heart Association (NYHA) classification. Pulse oximetry was used to measure resting blood oxygen saturation (SO2).

Microvolt T wave alternans was analyzed in 102P during treadmill test while receiving their usual medications, including beta blocker therapy [18]. After careful skin preparation high-resolution electrodes (Micro-V Alternans Sensors, Cambridge Heart Inc.) were applied using Frank orthogonal configuration. MTWA was recorded during a heart rate (HR)-based exercise protocol using CH2000 (Cambridge Heart Inc., Bedford, MA, USA) with the use of spectral method [14]. The test was considered positive if the significant MTWA (i.e. alternans voltage ≥ 1.8 μV and alternans ratio > 3.0) appeared at an onset HR ≤ 110 bpm, was present for ≥1 min in any orthogonal lead or two adjacent precordial leads and sustained as long as HR remained above the patient specific onset HR. The test was classified as negative if sustained MTWA was absent at HR ≤ 110 bpm and if there was ≥1 min at HR ≥ 105 bpm of artifact-free trace (noise level < 1.8 μV, ectopy < 10%). Otherwise, the test was considered indeterminate and immediately repeated in order to reduce the number of such results. As generally accepted [18] indeterminate test may be caused either by patient factors (including: 1) excessive ectopy during exercise, 2) unsustained MTWA, 3) failure to achieve HR = 105 bpm) or technical factors (including: 1) a noisy recording, 2) failure to maintain HR between 105-110 bpm for ≥1 min). The indeterminate results due to technical factors were ultimately excluded from further analysis. Considering similar prognostic significance of tests classified as positive or indeterminate due to patient factors they were combined into a common group labeled ‘non-negative’ [MTWA(non-)] i.e. abnormal.

Transthoracic echocardiography was performed with VIVID 7 GE Medical System device, using 1.5-2.5Hz probe in 2D, M and Doppler modes. The diagnoses of anatomical anomalies were set according to the current recommendations of the European Society of Cardiology (ESC) [7]. Alike in other studies [19] the diagnosis of pulmonary arterial hypertension (PAH) was based on echocardiography. The estimation of pulmonary arterial pressure (PAP) was based on the peak velocity of the jet of tricuspid regurgitation enabling to calculate right ventricular systolic pressure (using the simplified Bernoulli equation). After excluding pulmonary stenosis, PAP was calculated as the sum of right ventricular systolic pressure and right atrial pressure (estimated as 5-15 mmHg depending on the diameter and respiratory variation of the inferior vena cava). According to the current guidelines on PAH management, we considered the criterion of estimated PAP ≥ 37 mmHg combined with additional echocardiographic variables suggestive of PAH a sufficient basis to set this diagnosis [20].

Cardiopulmonary exercise treadmill test was performed according to the modified Bruce protocol (adding stage 0-3 min, 1.7 km/h, 5% grading) and symptom limited. The equipment was calibrated with a standard gas mixture before each test. Patients were encouraged to continue the exercise until the respiratory exchange ratio (RER) exceeded 1. Oxygen uptake (PeakVO2), carbon dioxide production (VCO2) and minute ventilation were measured with breath by breath technique using Sensor Medics, model Vmax29. Peak VO2 was defined as the average for the last 20s of exercise and expressed as ml/kg/min and ml/min, as well as the percentage ranges predicted for sex, age, height and weight [21]. A ventilation/carbon dioxide slope (VE/VCO2 slope) was assessed by linear regression for the whole exercise. A standard 12-lead electrocardiography was continuously recorded. Due to physical disability cardiopulmonary test was not performed in three patients.

Ambulatory 24-hour ECG monitoring was registered the same day as other tests using system CardioScan12.0 Premier, Oxford, 12.4.0040a version. Additionally, all previous results of ambulatory ECG available in the patient’s medical records were analyzed for presence of VA, which was classified as: excessive ventricular ectopy (ventricular premature beats – VPB ≥ 10/hour), episodes of nonsustained ventricular tachycardia – nsVT (presence of ≥3 consecutive ventricular beats at a rate greater than 100 bpm, terminating spontaneously in less than 30s), episodes of sustained ventricular tachycardia – sVT (ventricular tachycardia greater than 30s in duration or hemodynamically unstable) [6]. According to the classification regarding patients with structural heart disease [6,22] this findings were divided into two groups: potentially malignant ventricular arrhythmia (VPB ≥ 10/hour and/or nsVT) and malignant ventricular arrhythmia (sVT). For the purposes of analysis, a group comprising of patients with any of the specified forms of VA was created and labeled ‘VPB ≥ 10/hour/nsVT/sVT’.

QRS duration was adopted as the longest value measured among all 12 leads in standard electrocardiogram.

Serum brain natriuretic peptide (BNP) level was measured in the venous blood samples taken after 15 min of rest in supine position using the Abbott AxSYM Immunoassay system.

Statistical analysis. Continuous variables were summarized by mean ± SD or median and minimal-maximal values, depending on normality of distribution assessed with Wilk-Shapiro test. Variables following normal distribution were analyzed using Student’s t test or Welch test, otherwise nonparametrical U Mann–Whitney test comparing two groups was used. Categorical variables are represented by frequencies and percentages. For 2 × 2 tables chi-square test with Yates’s correction or Fisher’s exact test were performed. Factors associated with non-negative MTWA were assessed by logistic regression. Because some subgroups were too small it was impossible to perform multivariable logistic regression model for all parameters entered into analysis. Two-tailed values of p < 0.05 were considered statistically significant. Analyses were performed using the Statistica 7.0 package.

Informed consent was obtained from all subjects. Our study protocol, as approved by the Ethics Committee of University of Medical Sciences in Poznan, conformed to the ethical guidelines of the 1975 Declaration of Helsinki.

Results

The MTWA examination was performed in total of 102 patients and 45 healthy individuals. The MTWA(+) as well as MTWA(ind) was significantly more frequent in the study group than among controls (respectively: 18(17.6%) vs 1(2.2%), p = 0.008 and 18(17.6%) vs 0(0.0%), p = 0.002) (Table  1). Ultimately, 10 patients and 2 controls with MTWA indeterminate due to technical factors were excluded from further calculations and the rest constituted two groups under analysis.

Table 1

Microvolt T wave alternans in the study and control groups

	Study group (n = 102)	Control group (n = 45)	Study group vs control group p
MTWA(+) (%)	18 (17.6)	1 (2.2)	0.008
MTWA(ind) (%)	18 (17.6)	0 (0)	0.002
MTWA(noise) (%)	10 (9.8)	2 (4.4)	0.35
MTWA(−) (%)	56 (54.9)	42 (93.4)	0.00001
MTWA(non -) (%)	36 (35.3)	1 (2.2)	0.00001

MTWA(+) – positive result; MTWA(ind) - result indeterminate due to patient factors; MTWA(noise) – result indeterminate due to technical factors; MTWA(−) –negative result; MTWA(non-) – non-negative (abnormal) result.

As shown in Table  2 the number of males among patients with MTWA(+) and MTWA(non-) was significantly higher than in MTWA(−) group (respectively: 72.2% vs 33.9%, p = 0.006 and 58.3% vs 33.9%, p = 0.03). Patients with MTWA(non-) presented a higher NYHA class comparing to those with MTWA(−) [2.0(min1.0-max3.0) vs 1.0(min1.0-max3.0), p = 0.04] and lower resting SO2 [94.5%(min73-max100) vs (97%(min76-max100), p = 0.047].

Table 2

Relationship between MTWA result and demographic or clinical features in the analyzed group

	Analyzed group (n=92)	MTWA (+) (n = 18)	MTWA (ind) (n = 18)	MTWA (−) (n = 56)	MTWA (non-) (n = 36)	MTWA(+) vs MTWA(−) p	MTWA(non-) vs MTWA(−) p
Males (%)	40 (43.5)	13 (72.2)	8 (44.4)	19 (33.9)	21 (58.3)	0.006	0.031
Age (years)	29	28	31,5	29	29.5	0.782	0.620
Median	(18–75)	(19–64)	(20–75)	(18–74)	(19–22)
Min-max
Operated (%)	28 (27.5)	9 (50)	4 (22.2)	9 (50)	13 (36.1)	0.786	0.663
NYHA	1.0	2.0	2.0	1.0	2.0	0.231	0.040
Median	(1.0-3.0)	(1.0-3.0)	(1.0-3.0)	(1.0-3.0)	(1.0-3.0)
Min-max
SO2 (%)	97	96	92.5	97	94.5	0.151	0.047
Median	(69–100)	(75–99)	(73–99)	(69–100)	(73–100)
Min-max
Pulmonary hypertension (%)	11 (12.0)	1 (5.6)	7 (38.9)	9 (16.1)	2 (5.6)	0.434	0.191
Beta blocker (%)	25 (27.1)	7 (38.9)	3 (16.7)	15 (26.8)	10 (27.8)	0.380	1.0
QRS (ms)	120	120	135	120	125	0.354	0.123
MedianMin-max	(80–200)	(100–200)	(100–180)	(80–200)	(100–200)

MTWA(+) – positive result; MTWA(ind) – indeterminate result; MTWA(−) –negative result; MTWA(non-) – non-negative result; SO2 – blood oxygen saturation.

Malignant ventricular arrhythmia occured significantly more often in patients with abnormal compared to negative MTWA [7(19.4%) vs (2(3.6%), p = 0.026]. However, comparison between incidence of other forms of VA among subgroups characterized by different MTWA result did not show statistical significance (Table  3).

Table 3

Relationship between MTWA result and incidence of ventricular arrhythmia in the analyzed group

	Analyzed group (n = 92)	MTWA (+) (n = 18)	MTWA (ind) (n = 18)	MTWA (−) (n = 56)	MTWA (non-) (n = 36)	MTWA(+) vs MTWA(−) p	MTWA(non-) vs MTWA(−) p
VPB ≥ 10/h/nsVT (%)	23 (25.0)	3 (16.7)	9 (50.0)	11 (19.6)	12 (33.3)	1.0	0.217
sVT (%)	9 (9.9)	1 (5.7)	6 (33.3)	2 (3.6)	7 (19.4)	1.0	0.026
VPB ≥ 10/h/nsVT/sVT (%)	27 (29.3)	4 (22.2)	11 (61.1)	12 (21.8)	15 (41.7)	1.0	0.060

MTWA(+) – positive result; MTWA(ind) – indeterminate result; MTWA(−) – negative result; MTWA(non-) – non-negative result; VPB ≥ 10/h – excessive ventricular ectopy; nsVT – non-sustained ventricular tachycardia; sVT – sustained ventricular tachycardia.

In our study group the incidence of negative MTWA decreased along with the rise in NYHA scale (NYHA I −60.7%, II −32.1%, III −7.2%). Cardiopulmonary test showed that exercise tolerance measured with peak oxygen consumption (expressed as percentage of predicted values) was worse in patients with abnormal compared to those with negative MTWA: %PeakVO2 ml/kg/min (57.4 ± 11.7% vs 64.7 ± 17.0%, p = 0.029), %PeakVO2 l/min (58.7 ± 15.4% vs 66.4 ± 17.1%, p = 0.034). The difference was also revealed with regard to chronotropic response which was worse among subjects with abnormal compared to normal MTWA: HRmax (145.5 ± 26.1 bpm vs 160.1 ± 20.9 bpm, p = 0.016), %HRmax (81.4 ± 11.7% vs 88.8 ± 11.0%, p = 0.003). Patients with MTWA(non-) also had higher (reaching statistical significance) concentrations of serum BNP [57.1 pg/ml(min23.3-max343.5) vs 42.2 pg/ml (min6.6-max598.4), p = 0.052] (Table  4).

Table 4

Relationship between MTWA result and cardiopulmonary parameters or serum BNP concentration in the analyzed group

	Analyzed group (n = 92)	MTWA(+) (n = 18)	MTWA (ind) (n = 18)	MTWA(−) (n = 56)	MTWA (non -) (n = 36)	MTWA(+) vs MTWA(−) p	MTWA(non-) vs MTWA(−) p
BNP (pg/ml)	45.1	41.9	64.4	42.2	57.1	0.247	0.052
Median	(6.6-598.4)	(23.3-150.8)	(25.1-343.5)	(6.6-598.4)	(23.3-343.5)
Min-max
PeakVO2 (ml/kg/min)	23.9 ± 6.7	23.1 ± 5.5	21.5 ± 6.9	24.9 ± 6.9	22.3 ± 6.2	0.317	0.072
Mean ± SD
%PeakVO2 (ml/kg/min)	62.3 ± 17.3	57.6 ± 9.6	57.2 ± 13.9	64.7 ± 17.0	57.4 ± 11.7	0.098	0.029
Mean ± SD
PeakVO2 (l/min)	1.6 ± 0.6	1.6 ± 0.5	1.4 ± 0.7	1.6 ± 0.6	1.5 ± 0.6	0.845	0.376
Mean ± SD
%PeakVO2 (l/min)	64.0 ± 18.8	57.4 ± 12.7	60.0 ± 18.2	66.4 ± 17.1	58.7 ± 15.4	0.046	0.034
Mean ± SD
HRmax	154.3 ± 24.0	153.4 ± 27.0	137.1 ± 22.9	160.1 ± 20.9	145.5 ± 26.1	0.280	0.016
Mean ± SD
%HRmax	85.9 ± 11.8	85.0 ± 10.8	77.6 ± 11.8	88.8 ± 11.0	81.4 ± 11.7	0.200	0.003
Mean ± SD
VE/VCO2slope	32	32.5	42	32	36	0.118	0.061
Median	(22–60)	(26–60)	(26–59)	(22–58)	(26–60)
Min-max

MTWA(+) – positive result; MTWA(ind) – result indeterminate due to patient factors; MTWA(−) – negative result; MTWA(non-) – non-negative result; BNP – brain natriuretic peptide; HRmax – maximal heart rate on exercise; PeakVO2 – peak oxygen uptake on exercise; VE/VCO2 slope – ventilation/carbon dioxide slope.

As shown in univariate logistic regression analysis (Table  5), malignant VA was the most powerful factor to increase probability of abnormal MTWA (OR = 6.4, p = 0.029). This risk was also over twice as high in males (OR = 2.7, p = 0.021), in patients with any form (malignant and/or potentially malignant) of VA (OR = 2.6, p = 0.49) and in NYHA class > I (OR = 2.06, p = 0.033). Cardiopulmonary parameters also played a significant role, but to a lesser extent: HRmax (OR = 0.97, p = 0.006), %HRmax (OR = 0.94, p = 0.005), %PeakVO2 (OR = 0.97, p = 0.042), VE/VO2slope (OR = 1.05, p = 0.037). A multivariate logistic regression analysis with regard to the presence of abnormal MTWA confirmed a significant predictive value of sVT (OR = 20.7, p = 0.037) and male gender (OR = 15.9, p = 0.001).

Table 5

Factors increasing probability of abnormal MTWA in uni- and multivariate linear logistic regression analysis

	Univariable analysis		Multivariable analysis
	OR (95% CI)	p	OR (95% CI)	p
sVT	6.4 (1.22 – 33.57)	0.029	20.74 (1.21 – 355.88)	0.037
Male gender	2.72 (1.15 – 6.46)	0.021	15.98 (3.20 – 79.74)	0.001
VPB ≥ 10/h/nsVT/sVT	2.56 (1.01 – 6.51)	0.049	0.96 (0.23 – 4.05)	0.956
NYHA	2.06 (1.06 – 4.00)	0.033	2.38 (0.81 – 7.00)	0.115
VE/VCO2 slope	1.05 (1.00 – 1.10)	0.037	1.06 (0.98 – 1.14)	0.154
HRmax	0.97 (0.95 – 0.99)	0.006	0.99 (0.96 – 1.02)	0.421
%HRmax	0.94 (0.91 – 0.98)	0.005	-	-
%PeakVO2 (l/min)	0.97 (0.94 – 0.99)	0.042	1.03 (0.98 – 1.09)	0.202

sVT – sustained ventricular tachycardia; VPB ≥ 10/h – excessive ventricular ectopy; nsVT – non-sustained ventricular tachycardia; VE/VCO2slope – ventilation/carbon dioxide slope; HRmax - maximal heart rate on exercise; PeakVO2 – peak oxygen uptake on exercise.

Discussion

Among the analyzed patients with the chosen forms of CHD characterized by pathology within right ventricle or single ventricle physiology, positive as well as indeterminate MTWA test were present in both 19.6%. These values exceeded those observed in the control group: MTWA(+) was present in 2.2% what corresponded with the results achieved in the previously published studies (2.1% and 5.5%) [23,24]. As there was no available analysis of spectral MTWA phenomenon among adults with CHD, the only comparison could be made to pediatric groups – Cheung et al. [17] assessed MTWA in 49 children after tetralogy of Fallot repair observing 14.2% positive and as much as 37% indeterminate (including those caused by technical artifacts) results. Alexander et al. [16] showed the incidence of positive MTWA in 14% and indeterminate – in 28% out of 50 pediatric patients with CHD, which came close to the outcomes of our study.

It has been proven that the prognostic value of positive and indeterminate results is comparable [15,18,25-27], therefore the majority of analyses interpret currently these results as a common group of non-negative, i.e. abnormal MTWA. In our study abnormal tests were observed in 39.2% of patients, which is markedly less than the values described in the SCD high risk groups of patients with advanced left ventricular non-congenital heart failure and reach 67%-73% [25-27]. Exercise capacity as well as age had a distinctive impact on these populations – over half (51.1%) of the analyzed group presented NYHA I functional class (NYHA II – 39,1%, NYHA III – 9,8%) and majority of them were in their forties, whereas patients assessed in the cited publications were in the sixth or seventh decade of life.

Our study showed that incidence of the malignant VA was significantly higher among patients with abnormal compared to negative MTWA. Moreover, the presence of sVT and, to a lesser extent, presence of any form of VA significantly increased the risk of abnormal MTWA phenomenon. However, similar findings were not confirmed by the study of pediatric CHD patients [17]. Ventricular arrhythmia registered on ambulatory ecg monitoring has not yet been found predictive of SCD in this population, this however might be linked to a low number of such tests performed [1,28]. Nevertheless, the prognostic value of Holter ecg refines when interpreted together with other clinical features conducive to malignant arrhythmia [28].

Therefore, our analysis was extended in order to determine which demographical and clinical features of possible prognostic value for SCD are characteristic for patients with abnormal MTWA. It has been shown that majority of subjects with non-negative result were males and male gender turned out to be a factor of a higher probability of this abnormal electrical phenomenon on multivariate regression analysis. As already proven men are more prone to die of SCD than women [6]. Moreover, male gender is also an acknowledged risk factor for life-threatening VA [29,30] as well as total mortality [1] among patients with CHD.

Patients with different MTWA results did not differ with regard to age. SCD incidence in general population increases one hundred-fold after 35th year of life [6], but in the analyzed population heart disease is present since birth and it is rather the complexity of a given defect that determines patient’s later medical history. Previous cardiosurgery did not influence patients’ MTWA results, but the study group included subjects with various anatomical cardiac anomalies that were operated with various methods. Therefore, patients who underwent a cardiosurgery (e.g. with Fontan method) did not necessarily exhibited better clinical outcome than unoperated patients with other anomalies.

Although widening of QRS complex plays a role in SCD risk stratification [9,31], our study demonstrated no significant difference in this parameter with regard to the presence of MTWA phenomenon.

MTWA outcomes in the context of patients’ exercise tolerance are worth focusing on as heart failure has been found to predict malignant VA and SCD in the population of CHD [7,30]. In this specific group not only left ventricular function becomes impaired, but often also morphologically right systemic ventricle, both of the chambers, or the so called single ventricle may become dysfunctional. We observed that the number of patients with negative MTWA systematically decreased between NYHA I and NYHA III groups. Higher NYHA class was also found to increase the probability of abnormal MTWA phenomenon. It has been proven that deterioration of patients’ functional status assessed with this classification has an adverse prognostic value with regard to SCD in this population [32-34], what suggests a potential role of MTWA assessment in the risk stratification algorithms [10]. Despite some methodological objections (lack of objective assessment), NYHA classification remains the most widely used tool to assess heart failure symptoms, including adults with CHD. Although our study group consisted of patients with complex forms of CHD, over half of them (51,1%) was rated as NYHA class 1. Similar results were obtained by other investigators – NYHA class 1 was reported by Piran et al. [35] in 40% of subjects with single or systemic right ventricle (mean age 28,6 ± 7,8 years), whereas Diller et al. [11] classified 49% of patients with different complex forms of CHD (mean age 33 ± 13 years) as being asymptomatic. Common underestimation of patients’ self-reported functional status is mostly caused by lifelong adaptations to their heart disease and not being aware of slowly progressing exercise intolerance. Additionally, relatively young mean age of our study group (34,2 ± 13,6 years) makes NYHA Class 1 truly more possible as the symptoms of heart failure have not emerged yet. In contrast, the study conducted by Bolger et al. [36] among adults with complex CHD aged 33,5 ± 1,5 years revealed NYHA class 1 and 2 in, respectively, 21% and 59% of subjects. An explanation of such difference when compared to our results may be the fact that study group enrolled by us in almost one third consisted of patients with Ebstein syndrome, who are considered as being asymptomatic over decades [7], whereas this defect was not included into the study protocol by Bolger. Therefore, in such a heterogenous and not numerous population generalization and unequivocal conclusions are hardly possible.

The study design included also more reliable method of exercise tolerance evaluation i.e. cardiopulmonary test. The conclusions drawn from the analysis of these parameters were congruent with the findings based on NYHA classification - a significantly worse exercise capacity was observed among patients with abnormal MTWA compared to those with negative test, which manifested as lower peak oxygen uptake and worse chronotropic response in the former group. The mentioned parameters as well as an increased ventilatory respiratory workload (VE/VCO2 slope) raised the probability of abnormal MTWA in the analyzed group. Differences in BNP concentrations among groups varying with regard to MTWA result were not shown in our study.

Elevated pulmonary pressure along with decreased tissue oxygenation also contributes to the pathogenesis of heart failure among CHD patients [10], but since these phenomena often coexist, it is merely possible to analyze them separately [12]. In our trial patients with abnormal MTWA did not diverge from the rest in the incidence of pulmonary hypertension, but they were characterized by a markedly lower blood saturation. Experts’ opinion emphasizes that long-term cyanosis causes myocardial fibrosis which subsequently creates an arrhythmogenic substrate [12,34,37].

Study limitations

Our cohort is considerably smaller than those selected in previous studies on the prognostic value of MTWA, albeit due to the CHD population characteristics, most of performed clinical trials deal with heterogeneity and limited number of patients. As a consequence, the main limitation of our trial is lack of prospective evaluation of MTWA prognostic value with regard to SCD risk among adults with CHD. Taking into account a small number of patients combined with a low expected number of SCD per year, a statistically well-designed study would require to last at least 10 years [8,37]. Therefore, our analysis will be continued using mortality and arrhythmic end points and for the moment conclusions on the role of MTWA in CHD population can only be drawn indirectly, considering general knowledge on arrhythmic SCD and the data obtained in the study. On the basis of the results presented in our study one may also make an attempt to narrow down the group of adults with CHD who should undergo a careful evaluation of indications for ICD therapy, including MTWA test.

Conclusions

Abnormal spectral MTWA occurs significantly more often in the population of adults with congenital heart disease characterized by pathology within right ventricle or single ventricle physiology compared to healthy subjects.

The probability of its presence increases in patients with malignant ventricular arrhythmia and among subjects with clinical findings possibly related to lethal arrhythmia including advanced heart failure and cyanosis. Male gander is also associated with abnormal MTWA.

MTWA analysis might be of potential role in risk stratification algorithms for sudden cardiac death in this population, although further investigation in this field is required.

Competing interests

OT received funding from Servier. All other authors declare that they have no competing interests.

Authors’ contribution

AC, OT, AB conceived on the study idea, design and performed the data acquisition. AC conducted the literature review. AC, OT and LK conducted the statistical analysis and interpretation of data. AC and OT drafted the manuscript. All authors were involved in revising the article for important intellectual content and gave final approval of the version to be published.

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2261/13/26/prepub