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Cerebral oxygen delivery in newborns with congenital heart disease by phase contrast MRI

  • 1,
  • 1,
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Journal of Cardiovascular Magnetic Resonance201517 (Suppl 1) :M9

https://doi.org/10.1186/1532-429X-17-S1-M9

  • Published:

Keywords

  • Cerebral Blood Flow
  • Congenital Heart Disease
  • Vertebral Artery
  • Basilar Artery
  • Cerebral Oxygen Delivery

Background

Congenital heart disease (CHD) is associated with in utero brain dysmaturation and abnormal cerebral vasculature [1, 2]. Phase contrast (PC) MRI allows non-invasive quantification of cerebral blood flow (CBF) and, combined with arterial oxygen saturation (SaO2) and haemoglobin (Hgb) concentration, can measure cerebral oxygen delivery (CDO2). We hypothesized that CDO2 would be lower in newborns with CHD than normals.

Methods

We measured CBF and brain volume (BV) in 32 unsedated newborns (21 normals and 11 CHD) as part of an IRB approved study using a 1.5T Siemens Avanto MRI. CBF was measured according to a previously published technique using a single PC acquisition prescribed perpendicular to both internal carotid arteries (ICA) and basilar artery (BA) at the clivus level [3]. We also measured flows in the vertebral arteries (VA), common carotid arteries (CCA) and internal jugular veins (IJV) using a PC acquisition through the neck. Flows were quantified and indexed to BV calculated from a high resolution 3D T2W FSE acquisition. SaO2 and Hgb concentrations were measured using conventional blood gases in order to calculate: CDO2=SaO2×[Hgb]×1.36×CBF [4]. We compared net and indexed CBF and CDO2 in the two groups with an unpaired t-test with Welch's correction (Table 1). An analysis of CHD subgroups was also performed. The relationship between CBF and gestational age (GA) and agreement between BA vs VA flow sum was examined using Pearson's R.
Table 1

Table of mean values for all parameters measured, listed as mean ± SEM. P-values refer to comparisons of each subject group to the control group. The CHD subgroups are as follows: single ventricle physiology (SV), transposition of the great arteries (TGA), coarctation of the aorta (CoA), cyanotic and non-cyanotic CHD.

    

Net Value

 

Indexed to Brain Volume

 

Patient Type

Brain Volume (ml)

SaO2 (%)

Hgb (g/dL)

CBF (ml/min)

P-Value for CBF

CDO2 (mlO2/min)

P-Value for CDO2

CBF (ml/min/mlBV)

P-Value for CBF

CDO2 (mlO2/min/mlBV)

P-Value for CDO2

Normal (n=21)

395 ± 12

98

15

138 ± 14

 

2749 ± 284

 

0.341 ± 0.027

 

6.81 ± 0.54

 

CHD (n=11)

364 ± 14

90 ± 2.9

15.4 ± 0.44

118 ± 10

0.26

2191 ± 159

0.10

0.321 ± 0.020

0.56

5.99 ± 0.31

0.19

SV (n=4)

364 ± 31

85 ± 6.4

15.5 ± 1.1

122 ± 22

0.58

2101 ± 299

0.15

0.328 ± 0.036

0.78

5.69 ± 0.49

0.15

TGA (n=4)

347 ± 13

89 ± 1.5

15.1 ± 0.38

113 ± 13

0.23

2058 ± 199

0.06

0.329 ± 0.041

0.82

5.97 ± 0.63

0.34

CoA (n=3)

385 ± 28

99 ± 0.67

15.8 ± 0.73

117 ± 20

0.46

2487 ± 382

0.61

0.301 ± 0.032

0.38

6.40 ± 0.59

0.63

Cyanotic (n=7)

365 ± 14

85 ± 2.9

15.7 ± 0.46

124 ± 12

0.47

2198 ± 135

0.09

0.339 ± 0.027

0.96

6.04 ± 0.36

0.24

Non-Cyanotic (n=4)

361 ± 31

100 ± 0.5

15.0 ± 0.98

106 ± 18

0.22

2177 ± 411

0.29

0.290 ± 0.025

0.19

5.89 ± 0.66

0.31

Results

Subjects were scanned at a mean corrected GA of 40 weeks. MRI was performed prior to cardiac surgery in all CHD subjects. The two groups had no difference in GA (p=0.07). There were trends towards lower mean net and indexed CBF in CHD newborns compared with controls (control net CBF 138±14 vs CHD 118±10 ml/min (p=0.26), control indexed CBF 0.341±0.027 vs CHD 0.321±0.020 ml/min/mlBV (p=0.56)) (Table 1, Figure 1a,b). A similar trend in mean net and indexed CDO2 was observed in CHD newborns compared with controls (control net CDO2 2749±284 vs CHD 2191±159 mlO2/min (p=0.1), control indexed CDO2 6.81±0.54 vs CHD 5.99±0.31 mlO2/min/mlBV (p=0.19)) (Figure 1c,d). In keeping with one previous study (3), CBF increased with GA (r=0.7, p=<0.0001). The VA and BA flows were highly correlated (r=0.8, p=0.0002), indicating good accuracy of the PC assessment of CBF. There were no significant differences in measured parameters between subgroups of CHD.
Figure 1
Figure 1

CHD vs control comparisons of parameters plotted against corrected gestational age measured in weeks. a) Net cerebral blood flow (ml/min) vs gestational age; b) Indexed cerebral blood flow to pre-operative brain volume (ml/min/mlBV) vs gestational age; c) Net cerebral oxygen delivery (mlO2/min) vs gestational age; d) Indexed cerebral oxygen delivery to pre-operative brain volume (mlO2/min/mlBV) vs gestational age. There is a trend in each parameter towards decreased values in CHD subjects compared to control.

Conclusions

Although the differences between CBF and CDO2 in this small sample of subjects were not statistically significant, there was a clear trend towards lower values for both parameters in CHD subjects. We propose that with a larger sample size, these differences will be significant, in keeping with a demonstrable relationship between cerebral oxygenation and brain maturation in CHD fetuses and newborns.

Funding

N/A.

Authors’ Affiliations

(1)
The Hospital for Sick Children, Mississauga, ON, Canada

References

  1. Miller S, et al: N Eng N Med. 2007Google Scholar
  2. Kinnear C, et al: Circulation. 2008Google Scholar
  3. Varela M, et al: NMR in Biomedicine. 2012Google Scholar
  4. Rudolph AM, et al: Congenital Diseases of the Heart. 2009, WileyView ArticleGoogle Scholar

Copyright

© Lim et al; licensee BioMed Central Ltd. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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