Abstract
Purpose of this study was to investigate a potential correlation between the pattern of cerebral veins (CV) on susceptibility-weighted imaging (SWI) and blood oxygen saturation, as well as preoperative brain injury, in neonates with transposition of the great arteries (TGA). Eleven neonates with TGA underwent MRI preoperatively, including SWI, T1- and T2-weighted scans. Images were retrospectively evaluated and appearance of CV was graded from 0 (normal appearance) to 3 (severe prominent appearance). White matter injuries (WMI) and strokes were analysed. Results were correlated with preductal arterial oxygen saturation. As findings one subject showed a normal CV appearance (grade 0) whereas 10 showed pathological prominent CV (grades 1ā3); median 2. Mean oxygen saturation ranged between 67.5% and 89.0% (median 81.0%). CV grade and mean oxygen saturation correlated significantly (pā=ā0.011). WMI were absent in 5 cases, mild in 4, and moderate in 2 cases. We conclude, that SWI has the potential to be used to estimate the current hypoxic burden on brain tissue in TGA newborns by assessing the prominence of the CV.
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Introduction
Severe congenital heart disease (CHD) is a common cause of childhood morbidity with a prevalence of 8 per 1000 live births in Europe1. Advances in diagnostics, cardiac surgery and intensive care medicine have significantly reduced mortality by enabling early surgical repair of most severe defects2,3. In neonates with transposition of the great arteries (TGA), the neonatal arterial switch operation for correction is widely performed because it has good cardiovascular and survival outcomes. However, neurodevelopmental disabilities have emerged as the most common long-term complication of CHD in the surviving subjects4,5. Neurocognitive impairment affects many functions, e.g. executive function, motor development, memory and attention6,7. More than 50% of neonates with CHD show neurological abnormalities preoperatively8. Conventional MRI studies showed that brain injury with white matter lesions and cerebral strokes occurred before surgery in newborns with CHD9,10,11,12,13,14. A possible cause is preoperative hypoxia15,16,17. Studies using advanced MRI techniques revealed further abnormalities, e.g. reduced or diminished white matter microstructure in adolescents with CHD, using diffusion tensor imaging (DTI)18, or elevated lactate in neonates with CHD, using magnetic resonance spectroscopic imaging (MRSI)19. Susceptibility-weighted imaging (SWI) is a relatively new, but already well-established sequence. It is a high-resolution gradient-echo (GRE) MRI sequence with fully velocity-compensated pulse. Differences in the susceptibility properties of various tissues can be differentiated by post-processing the magnitude images using a phase mask, thereby emphasizing the magnetic properties of different susceptibility effects. SWI has improved diagnostic accuracy, e.g. through detecting and evaluating intracranial haemorrhage, haemorrhagic transformation of stroke or calcification20,21,22. In the cerebral veins (CV), decreased oxygen saturation correlates with an increase of de-oxygenated haemoglobin that leads to a prominent appearance of these veins23. This phenomenon is used for diagnostic purposes. Prominent CV were described in stroke patients in the perfusion-disturbed areas after thromboembolic occlusion20,21,22,23,24 and in patients with hemiplegic migraine25 due to hypoperfusion. The opposite effect, with diminished CV, was demonstrated in patients with hyperperfusion in status epilepticus and in hyperventilated patients26,27. A correlation between blood oxygen levels and prominence of CV has been also described27,28. Changes in blood oxygenation levels are well-known to also affect the signal intensity of cerebral veins in SWI29. Kitamura et al. introduced at first a scoring system of āprominence of veinā using SWI to asses neonatal hypoxic ā ischemic injury. In this study a correlation of patients with āabnormalā āprominence of veinā and abnormal intermediate-term to long-term neurologic outcome was found30. Neonates with TGA suffer from low arterial oxygen saturation. It is assumed that the degree and duration of preoperative hypoxia is a risk factor for later neurocognitive deficits8. While white matter lesions in MRI scans reveal chronic brain injury, the prominence of CV in the SWI is a dynamic feature of the current shortage of oxygen supply.
Given these points, the aim of this study was to investigate whether a presumed general prominence of CV could be used diagnostically to estimate the current hypoxic burden on brain tissue. We hypothesized a correlation between the preoperative oxygen saturation in patients suffering from TGA and the prominence of CV in SWI, which reflects the deoxygenated share of haemoglobin. Further, a correlation between preoperative brain injury (amount of white matter lesions) and the grading of prominence of CV was analysed.
Materials and Methods
Patient data
The retrospective study was approved by the local Ethics Committee (Kantonale Ethikkommission Bern, Switzerland) and was carried out according to the Declaration of Helsinki31. An informed consent of the patients was not necessary due to the retrospective study design.
Subjects who met the inclusion criteria for this descriptive case study were term neonates with confirmed TGA who underwent routine preoperative MRI, and were hospitalized in our paediatric intensive care unit. Only neonates with TGA were included, because of the quite similar circulation anomaly in these patients, but variable blood oxygen saturation. During the MR examination all patients were sedated with either midazolam i.v. (total dose between 0.1āmg and 3.1āmg) and/or chloral hydrate p.o. (total dose between 60āmg and 300āmg). In individual cases rocuronium i.v. and/or ketamine i.v. was injected (up to 3.2āmg, and up to 3.5āmg, respectively). None of the children received propofol medication, because of the risk for propofol infusion syndrome. Mandatory sequences for this study were SWI, T1- and T2-weighted images. A further inclusion criterion was availability of values for arterial oxygen saturation (measured by means of both arterial blood gas analysis and pulse oximetry) and arterial carbon dioxide (CO2) (measured by means of arterial blood gas analysis) that had been recorded on the same day that the patient underwent MRI. Concentrations of serum glucose in mmol/L, blood haemoglobin in g/L, blood pH, and heart rate in beats/min were noted. Further, for a higher objectivity three values of preductal peripheral oxygen saturation (SaO2) during or close to MRI examination were determined: first the blood arterial oxygen saturation (blood gas analysis data closest to SWI acquisition time), second the single peripheral oxygen saturation measurement (pulse oximetry data closest to SWI acquisition time), and third the mean of peripheral oxygen saturation measurements, measured in between 2āh before and after SWI acquisition (pulse oximetry data). Patient data were excluded if image quality was poor, e.g. due to motion artifacts, if MRI data had not been acquired due to cardiovascular instability, or if the patient had a complex form of TGA, e.g. TGA with a single ventricle.
Data acquisition
All imaging studies were performed using 1.5āT Siemens scanners (Magnetom Avanto and Magnetom Aera; Siemens Medical Solutions, Erlangen, Germany) with 12-channel head coils. The MRI protocol included axial SWI, T1 turbo spin echo (TSE) and T2 TSE. The following parameters were used.
Magnetom Avanto
SWI parameters: TR 49 ms, TE 40 ms, FoV read 230āmm, FoV phase 68.8%, voxel size 0.9āmmāĆā0.7āmmāĆā1.2āmm, slice thickness 1.2āmm, acquisition time 5:07āmin. The SWI and minimum intensity projection (mIP) images were generated automatically by the scanner software. T1 TSE parameters: TR 1000 ms, TE 13 ms, FoV 200āĆā200, slice thickness 3āmm, acquisition time 4:51āmin. T2 TSE parameters: TR 4260 ms, TE 113 ms, FoV 200āĆā200, slice thickness 3āmm, acquisition time 4:43āmin. Diffusion-weighted imaging (DWI) parameters: TR 6400 ms, TE 89 ms, FoV 230āĆā230, slice thickness 3āmm, acquisition time: 2:54āmin.
Magnetom Aera
SWI parameters:TR 49 ms, TE 40 ms, FoV read 230āmm, FoV phase 90.6%, voxel size 0.9āmmāĆā0.9āmmāĆā2.0āmm, slice thickness 2.0āmm, acquisition time 3:27āmin. The SWI and mIP images were generated automatically by the scanner software. T1 TSE parameters: TR 1380 ms, TE 12 ms, FoV 200āĆā200, slice thickness 3āmm, acquisition time 4:47āmin. T2 TSE parameters: TR 4380 ms, TE 107 ms, FoV 200āĆā200, slice thickness 3āmm, acquisition time 2:50āmin. DWI parameters: TR 5700 ms, TE 64 ms, FoV 230āĆā230, slice thickness 4āmm, acquisition time: 3:31āmin.
Data analysis
MRI sequences for all patients were reviewed independently by two board-certified neuroradiologists (RKV and DK for SWI, T1-weighted and T2-weighted images; RKV and CW for DWI). Other than knowing that these were TGA cases, they were blinded to the clinical course. MRI scans were assessed on our picture archiving and communication system (PACS) separately, in a standardized order: first SWI, followed by T1-weighted and T2-weighted images. When examining the SWI, both neuroradiologists classified the global prominence of CV according to 4 grades in the minimum intensity projection images (mIP): Grade 0: normal signal intensity, number, and diameter of cortical veins and deep veins (one or more veins up to 0.9āmm and 1.1āmm in diameter, respectively); no visible veins in the semioval centre. Grade I: slightly decreased signal intensity, increased number and diameter of cortical veins and deep veins (one or more veins up to 1.1āmm and 1.3āmm in diameter, respectively); virtually no visible veins in the semioval centre. Grade II: moderately decreased signal intensity, increased number and diameter of cortical veins and deep veins (one or more veins up to 1.4āmm and 1.7āmm in diameter, respectively); slightly to moderately visible veins in the semioval centre. Grade III: distinctly decreased signal intensity, increased number and diameter of hypointense cortical veins and deep veins (one or more veins up to 1.7āmm and 2.4āmm in diameter, respectively); distinctly visible veins in the semioval centre (see Fig.Ā 1). This grading might vary depending on individual anatomical conditions, the strength of the magnetic field or the MR manufacturer, and therefore be imprecize. Hence, we included further typical characteristics of prominent CVA (increased number of cerebral veins, increased signal intensity of cerebral veins, increased diameter of cerebral veins, and visible veins in the semioval centre) for a more objective and differentiated grading. Further, for two reasons we did not exactly use the āprominence of veinā scoring system introduced by Kitamura et al.30, but modified it. For evaluation only the deep medullary veins were used in this system. Meanwhile many studies have revealed the usefulness of both cortical and deep veins for evaluation of vein prominence22,23,24,25. For a higher sophistication we included these veins in our scoring system. Secondly, in some recently published studies diminished cerebral veins occur in case of a higher cerebral blood flow or increased oxygen supply most likely resulting in higher oxygenated haemoglobin levels26,27,28. Since TGA patients suffer from low oxygen saturation levels, leading to increased deoxygenated haemoglobin levels, we have not applied Grade 1 of the Kitamura scoring (absent deep medullary veins).
For evaluation of white matter injuries (WMI) and cerebral strokes we used a score previously described by McQuillen et al.13. In T2- and T1-weighted images, WMI and white matter strokes were analysed and counted: WMI were defined as lesions measuring <2āmm of abnormal T1-hyperintensity or of low intensity on T1-weighted images in the absence of marked T2-hypointensity13,16. Severity of WMI was classified as absent (0 areas of T1 signal abnormality); mild (ā¤3 areas of T1 signal abnormality measuring <2āmm); moderate (>3 areas of T1 signal abnormality measuring <2āmm or areas of T1 signal abnormality measuring >2āmm but covering <5% of the cerebral hemisphere); or severe (T1 signal abnormality covering >5% of the cerebral hemisphere) (see Fig.Ā 2A to C). Cerebral strokes were defined as focal regions of ā„3āmm with or without diffusion restriction on DWI12 (see Fig.Ā 2D to F). In a final session, a consensus reading was performed in cases of disagreement.
Statistical analysis
For statistical analysis the SPSS statistics software package was used (IBM, Armonk, N.Y., USA). A non-parametric, two-sided Kendall rank correlation coefficient test was applied to verify whether the two variables (prominence of CV and arterial blood oxygen levels) were statistically dependent. A p-value of <0.05 was considered significant. Median and total range for all parameters was determined (SWI grade, WMI, white matter strokes, arterial blood oxygen saturation, arterial blood pCO2, blood glucose, blood haemoglobin, blood pH, single monitored oxygen saturation measurement, and mean monitored oxygen saturation value).
For interrater reliability of findings in SWI, T1w and T2w sequences in MRI scans, a Cohens-Kappa test was performed and the interrater reliability was classified according to Landis and Koch32.
Data availability
The datasets generated during and/or analysed during the current study are not publicly available due to preclusion from dissemination following Swiss Federal Law Regulations, but are available from the corresponding author on reasonable request.
Results
Subjects and clinical data
Between March 2011 and July 2015, 11 patients (8 male and 3 female; mean age 5.7 days at time of MRI acquisition) fulfilled the inclusion criteria.
Arterial blood oxygen saturation ranged between 66.0 and 88.0% (median 75%; nā=ā11) and was low in all subjects (normal range 93ā98%). Monitored preductal single oxygen saturation value closest to the time of SWI acquisition ranged between 64.0% and 86.0% (median 84.5; nā=ā10), and monitored mean preductal oxygen saturation values (measured in between 2āh before and after SWI acquisition) ranged between 68.0% and 89.0% (median 82.0%; nā=ā10).
Arterial pCO2 ranged between 36 and 55āmm Hg (median 41āmm Hg; nā=ā11). Blood glucose ranged between 4.5 and 6.3āmmol/L, median 5.2 (nā=ā10). Haemoglobin values were between 124 and 177āg/L, median 144 (nā=ā11). pH ranged between 7.34 and 7.45, median 7.37 (nā=ā11); see TableĀ 1 for details.
Blood CO2 and blood haemoglobin were in the upper standard value range in 2 subjects. Blood glucose was normal in all patients.
Imaging findings
One subject showed a normal cerebral veins appearance (CVA) (grade 0) while 10 showed prominent CVA (4 patients with grade 1, 4 patients with grade 2, and 2 patients with grade 3); range between grade 0 and 3; median 2. Severity of WMI was graded as absent in 5 cases with no WMI, mild in 4, and moderate in 2 cases. Only one patient showed white matter strokes in the territory of the left middle cerebral artery with 3 lesions >2āmm. Furthermore, in one patient two acute ischaemic areas were found, in 3 patients 1 acute ischaemic area was found and 7 patients had no acute ischaemia (TableĀ 1).
Patient No. 8 underwent follow-up MR imaging postoperatively, with an oxygen saturation of 95% and a normalized CV appearance Grade of 0 (see Fig.Ā 3B).
Statistical analysis
The interrater reliability was high (Kappaā=ā0.869 [pā<ā0.001]) for the grade of cerebral venous prominence in SWI, as well as for the WMI in T1-weighted and T2-weighted images (Kappaā=ā0.861 [pā<ā0.001]). Interrater reliability for acute ischaemic findings was high too (Kappaā=ā0.907 [pā=ā0.02]).
Three values of oxygen saturation were analysed (Fig.Ā 4 for illustration): the blood arterial oxygen saturation (Fig.Ā 4A, blood data closest to SWI acquisition time), single peripheral oxygen saturation measurement (Fig.Ā 4B; pulse oximetry data closest to SWI acquisition time), and mean of peripheral oxygen saturation measurements, measuredāĀ±ā2āh of SWI acquisition (Fig.Ā 4C; pulse oximetry data). A significant correlation was found for blood arterial oxygen saturation (pā=ā0.01, Kendallās tauā=āā0.657; Fig.Ā 4A), and for mean peripheral oxygen saturation (pā=ā0.011, Kendallās tauā=āā0.680; Fig.Ā 4C), but not for single peripheral oxygen saturation, measurement closest to SWI measurement (pā=ā0.147, Kendallās tauā=āā0.401; Fig.Ā 4B) due to a statistical outlier (patient No. 6: SWI grade 3 and 86% SaO2).
No significant correlation was seen between severity of WMI and prominence of CV in SWI (pā=ā0.721,Kendallās tauā=ā0.099), nor was any significant correlation found between acute ischaemia in DWI and prominence of CV in SWI (pā=ā1.0, Kendallās tauā=ā0.0) or between CVA and blood CO2, blood glucose, blood haemoglobin, and blood pH (p-values between 0.243 and 0.679, Kendallās tau between ā0.302 and 0.194).
Discussion
The main finding of our investigation is a significant correlation between the prominence of CVA and blood oxygen saturation levels. In our study only one newborn showed a normal appearance of the CV, whereas 10 revealed a pathological venous pattern with presumed higher deoxyhaemoglobin levels, significantly correlating with the arterial blood oxygen saturation (blood arterial oxygen saturation and monitored mean oxygen saturation). Only monitored single oxygen saturation measurements showed no significant correlation, because of an outlier value (patient No. 6 with 86% oxygen saturation and prominence of CV of grade 3). To the best of our knowledge this is the first report showing a significant correlation between blood arterial oxygen saturation levels and the extent of prominent CV in SWI of newborns suffering from TGA. However, in a recently published study by Ćztoprak on 19 adult patients with pulmonary embolism, a significant correlation between presence of prominent veins on SWI and hypoxemia33 was found, which is in line with our results. Further, our findings are in accordance with a recently published experimental study by Patzig et al.34. In their study 16 healthy adult volunteers underwent MRI under room air conditions, short-term hypoxia (7āminutes before and during the MRI scan), and long-term hypoxia (8.5āhours before and during the MRI scan). The 9 subjects who were finally included in the study showed significantly lower signal intensities of CV in the scans under conditions of hypoxia. However, our study is the first to investigate a patient population with chronically low arterial blood oxygen levels.
Blood CO2 is another parameter with an influence on CVA. For example, in a recently published study, a correlation between hyperventilation (in which CO2 is expelled leading to a vasoconstriction with lower cerebral blood flow) and higher signal intensity in CV was demonstrated, indicating a lower venous blood oxygenation level during hyperventilation28. Sedlacik et al. revealed a significant correlation between high etCO2 and cerebral blood flow with weak venous contrast in SWI35 in spontaneously breathing patients sedated with propofol. Since etCO2 and blood bicarbonate levels show a significant correlation36, blood CO2 might have influenced the CVA in our study. The difference between etCO2 and PaCO2 is stated to be 2ā5āmm Hg with higher values for PaCO2 37. Based on the findings of Sedlacik et al. etCO2 should be kept as low as possible to obtain a good venous contrast in SWI. With a maximal etCO2 value of 30ā35āmmHg CBF in sedated children is not artificially elevated38,39. Although in our subjects, blood CO2 was normal, with a median of 41āmm Hg it might have influenced the CVA, even by subtracting 2ā5āmm Hg, since it is still higher than 30ā35āmm Hg and might lead to an increase of CBF. However, in case of an elevated blood CO2 and CBF a weak venous contrast would be expected. In our subjects a stronger venous contrast is observed, therefore we assume the influence of blood CO2 is presumably low to negligible. Further blood parameters with a potential to lead to bias were in the normal range (median of blood glucose 5.2āmmol/L; median of blood haemoglobin 144āg/L; and median pH of blood, 7.37). These findings indicate that the changes in CVA are most likely caused by the blood oxygen saturation levels, correlating with other investigations28,29,33,34.
Many studies have demonstrated that newborns with complex CHD have abnormal brain development with brain injuries and delayed brain maturation9,10,11. Preoperatively, neonates with TGA exhibit brain injury which is associated with hypoxia15,17. It can be assumed that if hypoxia improves in TGA patients, the neuroanatomical and developmental outcome improves too40. A technique currently used to reveal brain injury is MRI. Using diffusion-weighted T1w and T2w images, WMI and strokes can be detected. A correlation between WMI and neurological abnormalities has been described in neonates with severe CHD before surgery16. A study using magnetic resonance spectroscopy, which is an advanced neuroimaging technique, revealed an elevated lactate in neonates with TGA, indicating an abnormal brain metabolism19, even in subjects in whom MRI showed no evidence of preoperative brain injury. Diffusion tensor imaging studies revealed regions of reduced white matter9,18.
Our investigation showed no correlation of WMI, acute or chronic strokes, and SWI findings; e.g. patient No. 3 showed a clear discrepancy with 10 WMI lesions, but a mean oxygen saturation of 89% and a prominence of CV of grade 1. These results were expectable, since both the oxygen saturation measurement and the prominence of the CV provide a āsnapshotā reflecting the current hypoxic burden, while WMI or strokes are unique events leading to chronic gliotic tissue damage. Nine of 11 subjects had no WMI, or only one lesion, but 10 of the 11 showed a pathological cerebral venous pattern.
The prominence of CVA in neonates with TGA in SWI is a new finding in this context, indirectly demonstrating an abnormal oxygen supply. Compared to chronic changes such as WMI, SWI has the advantage that it can demonstrate current acute changes in venous haemoglobin composition by CVA (see Fig.Ā 3 as example). Therefore, SWI can potentially be used to estimate insufficient brain oxygen in neonates suffering from TGA, which might be important e.g. in postoperative control MRI to assess whether brain oxygen supply has improved. A relatively new method, for assessing cerebral oxygen saturation in neonates, is near-infrared spectroscopy (NIRS)41. Both techniques evaluate the āvenous weightedā cerebral haemoglobin values. NIRS has some clear advantages. It evaluates the cerebral oxygen saturation, is non-invasive, measures cerebral oxygen saturation continuously, and is as such a valuable bedside tool. However, NIRS has some limitations including a limited penetration depth of the NIR light, i.e. reaching the cerebral cortex only, the instability of NIRS values, and the lack of a direct reference against which to correlate the values42. This might lead to a false higher cerebral oxygen saturation values in individual cases. Further, the derived NIRS-signal contains extracerebral ācontaminationā from bone and skin tissue. SWI has the ability to detect prominent cerebral veins in the whole brain in a standardized manner and therefore provides additional clinically meaningful information, despite the more work-intensive data acquisition. Since a brain MRI in children with congenital heart disease is carried out anyway, SWI in this context can be acquired quite easily.
Our study does however have limitations. Cerebral metabolic rate of oxygen and cerebral blood flow were not measured during MRI acquisition. Although proprofol was not applied to our patients, we cannot fully rule out an influence on cerebral metabolism and cerebral blood flow, caused by an anesthesic used in our patients, as described in previous studies for midazolam, chloral hydrate or ketamine43,44,45. Midazolam can slightly decrease cerebral blood flow43, which might contribute to the prominence of CV, because of higher deoxygenated hemoglobin levels. In contrast, ketamine might lead to a mild increase of cerebral blood flow with no effect on the metabolic rate45, which might contribute to lesser prominent CVs. For chloral hydrate both, a decrease of cerebral blood flow (resulting in higher deoxygenated hemoglobin levels) and a decrease of cerebral glucose utilization (resulting in higher oxygenated hemoglobin levels) was described44. Hence, an effect on the prominence of CV on SW images is more likely neutralized.
Further, using a retrospective study design we analysed a standard SWI sequence and graded the prominence of CV visually. Although the outcome was in line with our hypothesis, a more objective quantification of venous prominence would be helpful. An example of a relatively new approach is quantitative susceptibility mapping (QSM), using SWI for measuring oxygen saturation; it was introduced by Haacke et al.46 and has the potential to provide quantitative estimations of oxygen saturation in CV. This technique uses phase images and has been applied to CV in stroke patients for estimation of oxygen saturation in a recent study47. Both SWI and QSM are gaining increasing acceptance in clinical practice48. In future studies, acquisition of SWI with phase images in neonates with TGA would help to quantify the extent of oxygen shortage in CV.
Another limitation of the present study is the small number of patients. A larger cohort is needed to confirm our results.
In conclusion, the appearance of prominent cerebral veins in SWI is a pathological finding in 10 of 11 newborns with TGA in our study. It indicates an increase of deoxygenated hemoglobin, and thus lack of oxygenated hemoglobin. Our study demonstrated a significant correlation between the appearance of CV in SWI and the arterial blood oxygen levels in neonates with TGA. SWI has the potential to be used to estimate the current hypoxic burden on brain tissue by the effect on the appearance of CV. As a dynamic sequence SWI reflects the oxygen shortage in a āsnapshotā, while other conventional sequences e.g. T1w or T2w images show chronic or subacute ischaemic changes. Therefore SWI might be a helpful additional sequence to the MRI protocol for TGA patients, to clarify the possibility and the extent of cerebral hypoxia (e.g before and after surgery), and rule out other intracranial pathologies, like hemorrhagic transformation of ischemic regions. Further studies with a larger cohort and SWI phase images would be beneficial to test our findings objectively by quantifying the cerebral venous oxygen saturation.
References
Samanek, M. Congenital heart malformations: prevalence, severity, survival, and quality of life. Cardiol. Young. 10, 179ā185 (2000).
Mahle, W. T., Spray, T. L., Wernovsky, G., Gaynor, J. W. & Clark, B. J. 3rd Survival after reconstructive surgery for hypoplastic left heart syndrome: a 15-year experience from a single institution. Circulation 102, 136ā141 (2000).
Weinstein, S. et al. Early survival of infants weighing 2.5 kilograms or less undergoing first-stage reconstruction for hypoplastic left heart syndrome. Circulation 100, 167ā170 (1999).
Donofrio, M. T., Duplessis, A. J. & Limperopoulos, C. Impact of congenital heart disease on fetal brain development and injury. Curr Opin Pediatr 23, 502ā511 (2011).
Tabbutt, S., Gaynor, J. W. & Newburger, J. W. Neurodevelopmental outcomes after congenital heart surgery and strategies for improvement. Curr Opin Cardiol 27, 82ā91 (2012).
Bellinger, D. C. et al. Developmental and neurological status of children at 4 years of age after heart surgery with hypothermic circulatory arrest or low-flow cardiopulmonary bypass. Circulation 100, 526ā532 (1999).
Hovels-Gurich, H. H. et al. Long term behavioral outcome after neonatal arterial switch operation for transposition of the great arteries. Arch Dis Child 87, 506ā510 (2002).
Limperopoulos, C. et al. Predictors of developmental disabilities after open heart surgery in young children with congenital heart defects. J Pediatr 141, 51ā58 (2002).
Miller, S. P. et al. Abnormal brain development in newborns with congenital heart disease. N Engl J Med 357, 1928ā1938 (2007).
Licht, D. J. et al. Brain maturation is delayed in infants with complex congenital heart defects. J Thorac Cardiovasc Surg 137, 529ā536 (2009).
Mahle, W. T. et al. An MRI study of neurological injury before and after congenital heart surgery. Circulation 106, 109ā114 (2002).
Block, A. J. et al. Clinically silent preoperative brain injuries do not worsen with surgery in neonates with congenital heart disease. J Thorac Cardiovasc Surg 140, 550ā557 (2010).
McQuillen, P. S. et al. Balloon atrial septostomy is associated with preoperative stroke in neonates with transposition of the great arteries. Circulation 113, 280ā285 (2006).
McQuillen, P. S. et al. Temporal and anatomic risk profile of brain injury with neonatal repair of congenital heart defects. Stroke 8, 154ā160 (2007).
Petit, C. J. et al. Preoperative brain injury in transposition of the great arteries is associated with oxygenation and time to surgery, not balloon atrial septostomy. Circulation 119, 709ā716 (2009).
Bertholdt, S. et al. Cerebral lesions on magnetic resonance imaging correlate with preoperative neurological status in neonates undergoing cardiopulmonary bypass surgery. Eur J Cardio Thor Surg 45, 625ā632 (2014).
Watanabe, K. et al. Impaired neuroanatomic development in infants with congenital heart disease. J Thorac Cardiovasc Surg 137, 146ā153 (2008).
Rollins, C. K. et al. White matter microstructure and cognition in adolescents with congenital heart disease. J Pediatr 165, 936ā944 (2014).
Miller, S. P. et al. Preoperative brain injury in newborns with transposition of the great arteries. Ann Thorac Surg 77, 1698ā1706 (2004).
Mittal, S., Wu, Z., Neelavalli, J. & Haacke, E. M. Susceptibility-weighted imaging: technical aspects and clinical applications, part 2. AJNR Am J Neuroradiol 30, 232ā252 (2009).
Santhosh, K. et al. Susceptibility weighted imaging: a new tool in magnetic resonance imaging. Clin Radiol 64, 74ā83 (2009).
Hermier, M. & Nighoghossian, N. Contribution of susceptibility-weighted imaging to acute stroke assessment. Stroke 35, 1989ā1994 (2004).
Xia, S. et al. Decreased oxygen saturation in asymmetrical prominent cortical veins in patients with cerebral ischemic stroke. Magn Reson Imaging 32, 1272ā1276 (2014).
Verma, R. K. et al. Leptomeningeal collateralization in acute ischemic stroke: impact on prominent cortical veins in susceptibility-weighted imaging. Eur J Rad 83, 1448ā1454 (2014).
Bosemani, T. et al. Pediatric hemiplegic migraine: role of multiple MRI techniques in evaluation of reversible hypoperfusion. Cephalalgia 34, 311ā315 (2014).
Aellen, J. et al. Focal hemodynamic patterns of status epilepticus detected by susceptibility weighted imaging (SWI). Eur Radiol 11, 3430ā3432 (2014).
Chang, K., Barnes, S., Haacke, E. M., Grossman, R. I. & Ge, Y. Imaging the effects of oxygen saturation changes in voluntary apnea and hyperventilation on susceptibility-weighted imaging. AJNR Am J Neuroradiol 35, 1091ā1095 (2014).
Bosemani, T., Verschuuren, S. I., Poretti, A. & Huisman, T. A. Pitfalls in susceptibility-weighted imaging of the pediatric brain. J Neuroimaging 24, 221ā225 (2014).
Rauscher, A., Sedlacik, J., Barth, M., Haacke, E. M. & Reichenbach, J. R. Nonnvasive assessment of vascular architecture and function during modulated blood oxygenation using susceptibility weighted magnetic resonance imaging. Magn Reson Med. 54(1), 87ā95 (2005).
Kitamura, G. et al. Hypoxic-ischemic injury: utility of susceptibility-weighted imaging. Pediatr Neurol. Oct;45(4):220ā4 (2011).
World Medical Association Declaration of Helsinki Ethical principles for medical research involving human subjects. Available via http://www.wma.net/en/30publications/10policies/b3/ Accessed 19 Aug 2016 (1964).
Landis, J. R. & Koch, G. G. The measurement of observer agreement for categorical data. Biometrics. 33(1), 159ā74 (1977).
Ćztoprak, B. Prominent cerebral veins on susceptibility-weighted imaging (SWI) in pulmonary embolism. Eur Radiol. 27(7), 3004ā3012 (2017).
Patzig, M. et al. Susceptibility-weighted angiography visualizes hypoxia in cerebral veins. Invest Radiol 50, 397ā400 (2015).
Sedlacik, J. et al. Attenuation of cerebral venous contrast in susceptibility-weighted Imaging of spontaneously breathing pediatric patients sedated with propofol. Am J Neuroradiol 31, 901ā06 (2010).
Taghizadieh, A. Comparison of end-tidal carbon dioxide and arterial blood bicarbonate levels in patients with metabolic acidosis referred to emergency medicine. J Cardiovasc Thorac Res. 8(3), 98ā101 (2016).
Soleimanpour, H., Gholipouri, C., Golzari, S. E. J., Rahmani, F. & Sabahi, M. Capnography in the Emergency Department. Emergency Med 2, e123, https://doi.org/10.4172/2165-7548.1000e123 (2012).
Karsli, C., Wilson-Smith, E., Luginbuehl, I. & Bissonnette, B. The effect of nitrous oxide on cerebrovascular reactivity to carbon dioxide in children during propofol anesthesia. Anesth Analg. 97(3), 694ā8 (2003).
Karsli, C., Luginbuehl, I. & Bissonnette, B. The cerebrovascular response to hypocapnia in children receiving propofol. Anesth Analg. Oct 99(4), 1049ā52 (2004).
Ibuki, K. et al. The improvement of hypoxia correlates with neuroanatomic and developmental outcomes: comparison of midterm outcomes in infants with transposition of the great arteries or single-ventricle physiology. J Thorac Cardiovasc Surg 143, 1077ā1085 (2012).
Dix, L. M., van Bel, F. & Lemmers, P. M. Monitoring Cerebral Oxygenation in neonates: An upgrade. Front. Pediatr. 14, 5:46 (2017).
Durandy, Y., Rubatti, M. & Couturier, R. Near Infrared Spectroscopy during pediatric cardiac surgery: errors and pitfalls. Perfusion. 26(5), 441ā6 (2011).
Veselis, R. A. et al. Midazolam changes cerebral blood flow in discrete brain regions: an H2(15)O positron emission tomography study. Anesthesiology. 87, 1106ā1117 (1997).
Nakao, Y. et al. Effects of anesthesia on functional activation of cerebral blood flow and metabolism. Proc Natl Acad Sci USA 19 98(13), 7593ā8 (2001).
Langsjo, J. W. et al. S-ketamine anesthesia increases cerebral blood flow in excess of the metabolic needs in humans. Anesthesiology. 103, 258ā268 (2005).
Haacke, E. M., Tang, J., Neelavalli, J. & Cheng, Y. C. Susceptibility mapping as a means to visualize veins and quantify oxygen saturation. J Magn Reson Imaging 32, 663ā676 (2010).
Hsieh, M. C. et al. Quantitative susceptibility mapping-based microscopy of magnetic resonance venography (QSM-mMRV) for in vivo morphologically and functionally assessing cerebromicrovasculature in rat stroke model. PLoS One 14;11(3) (2016).
Reichenbach, J. R., Schweser, F., Serres, B. & Deistung, A. Quantitative susceptibility mapping: concepts and applications. Clin Neuroradiol 25 (Suppl) 2, 225ā230 (2015).
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We thank Pietro Ballinari for statistical analysis.
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R.K.V., B.W., D.K., D.H. conceived and designed the study. D.H., C.W., R.K.V. performed the image acquisition. R.K.V., D.H., C.W., J.G., D.H., B.W. analyzed the data. J.G., R.W., B.W., D.H., S.B., S.G. contributed materials, imaging and clinical data, and analysis tools. R.K.V., B.W., D.K., D.H., S.B., S.G. wrote the paper. All authors reviewed the manuscript.
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Verma, R.K., Keller, D., Grunt, S. et al. Decreased oxygen saturation levels in neonates with transposition of great arteries: Impact on appearance of cerebral veins in susceptibility-weighted imaging. Sci Rep 7, 15471 (2017). https://doi.org/10.1038/s41598-017-15591-3
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DOI: https://doi.org/10.1038/s41598-017-15591-3
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