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Lower risk of hearing loss without sacrificing image quality in fetal MR imaging: a feasibility study using acoustic reduction technique
Le Cao1, Ting Liu1, Junjun Li1, Jingtao Sun1, Jianxin Guo1, Xiaocheng Wei2, and Jian Yang1

1The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, China, 2MR Research China, GE Healthcare, Bei Jing, China

Synopsis

3.0T MR scanner can achieve superior image quality depicting fetal anatomic details over 1.5T, but may poses higher risk of adverse impact on fetal auditory development due to its intrinsically higher acoustic noise level. This comparative study investigated the value of acoustic noise reduction technique in fetal exam. The result shows the technique can acquire equivalent quality images in 3.0T scanner, meanwhile decrease hearing loss risk in fetal head examinations compared with the conventional method.

Introduction

Since the first fetal MR imaging was performed in 19831, the technique has developed vastly in the past 3 decades with the improvement of fetus image quality. Previous studies suggested that there was no adverse effect of exposure to 1.5T MR imaging in utero on neonatal hearing function2, while Joel’s3 advised that it seems prudent to avoid more than 1.5T MRI for pregnant women. On the other hand, existing evidences indicate that compared to 1.5T MRI, 3.0T system achieves better anatomical delineation in fetal imaging. However, concern remains on the risk of hearing damage as well as aggravated fetal movement artifacts induced by the elevated acoustic noise level. How can we reduce the impact of noise while acquiring high resolution images in 3.0T? Our study compared the acoustic level and image quality with and without acoustic reduction technique (ART). The purpose of this study was to evaluate whether ART is reliable and applicable in fetus brain imaging.

Method

The Institutional Review Board approved this study and all the written informed consents were obtained from pregnant woman. Images were continuously collected from September 2017 to October 2018 using 3.0T MR scanner (Discovery 750W; GE Medical system, Milwaukee, WI) for fetal head exams. 10 subjects underwent ART sequences (group A), the matched 10 subjects underwent traditional sequences (group B). The protocol of tradition sequences includes T2 single short fast spin echo (SSFSE) (axial, sagittal, coronal); while the ART sequences contains ART T2 SSFSE (axial, sagittal, coronal) (Table1). The ART used in our study intentionally decrease the slew rate of gradient waveform from 12 Guass/cm/ms to 5 Guass/cm/ms to achieve lower acoustic noise level. Noise of each sequence at different sites was measured using a special noise meter (BSWA 801; Beijing Shengwang Acoustic and Electromagnetic Technology), each of which was tested for 20 seconds and measured continuously for 3 times for average value. A quantitative assessment by the ROI of 1 mm was manually placed on the different layers of the brain (Fig 1A): germinal matrix, periventricular layer, subplate layer, and cortical layer. The mean signal intensity for each layer was collected, and comparative ratio to air was calculated4. A qualitative evaluation including eight criteria (1. Delineation of germinal zone and gray matter, 2. Delineation of white matter, 3. Delineation of internal and external CSF spaces, 4. Delineation of amniotic fluid adjacent to the skull, 5.Delineation of brain stem, 6. Delineation of cerebellum, 7. Severity of motion artifacts, 8. Overall image quality) were evaluated on an ordinal scale regarding signal characteristics, potential dysmorphism and developmental anomalies (5= optimal diagnostic quality; 4= very good image quality;3= diagnostic image quality, 2= image quality below diagnostic standards; 1= image quality too poor to correctly identify anatomy)5. The noise and image quality differences between the two groups were compared. Statistical analysis was performed in SPSS 20.0 and P value less than 0.05 was considered to indicate statistical significance.

Results

There was no statistical difference between the demographic data of the two groups. The maximum differences of peak and equivalent sound pressure between the two groups are 18.1dBA and 16.1dBA respectively (Table2), indicating the ART sequences have lower noise than traditional sequences. Comparative ratios calculated between germinal matrix/air, periventricular layer/air, subplate layer/air, and cortical layer/air for group A (33.97±17.52, 42.45±16.65, 46.37±22.46, 43.03±20.89) were lower than that of group B (52.54±25.61, 33.39±12.91, 69.17±35.21, 64.76±32.53), but with no significant difference (P=0.09,0.20, 0.12, 0.11) (Fig1C-F). The qualitative results showed that the image quality of group B and group A scored 4.42 + 0.37 and 4.36 + 0.49 respectively(Fig1B). There was no significant difference in image quality score between the two groups. The detailed information is summarized in Table3.

Discussion

Committee on Environmental Health6 reported children with high-frequency hearing loss tested at 4 to 10 years of age were more likely to have been born to women who were exposed consistently to occupational noise in the range of 85 to 95 dBA during pregnancy. The noise of 3.0T gradient field can maximum reach 120dBA-130dBA. Noise can attenuate 20~30dBA through abdominal, uterine wall and amniotic fluid reaching the fetus. Our study shows peak sound pressure is 127.3dBA (traditional sequence) and 109.2 dBA (ART sequence). Considering the aforementioned attenuation, the noise for fetus may be less than 80 dBA during ART scan, meanwhile the high image quality can be maintained.

Conclusion

Acoustic reduction sequence can acquire high quality images in 3.0T scanner, meanwhile decrease hearing loss risk in fetal head examinations compared with the conventional method.

Acknowledgements

This study was supported by the National Key Research and Development Program of China (2016YFC0100300), National Natural Science Foundation of China (No. 81471631, 81771810 and 51706178), the 2011 New Century Excellent Talent Support Plan of the Ministry of Education, China (NCET-11-0438) and the Clinical Research Award of the First Affiliated Hospital of Xi’an Jiaotong University (No. XJTU1AF-CRF-2015-004).

References

1. Smith FW, Adam AH and Phillips WD. NMR imaging in pregnancy. Lancet. 1983; 321: 61-2.

2. Strizek B, Jani JC, Mucyo E, et al. Safety of MR Imaging at 1.5 T in Fetuses: A Retrospective Case-Control Study of Birth Weights and the Effects of Acoustic Noise. Radiology. 2015; 275: 530.

3. Ray JG, Vermeulen MJ, Bharatha A, Montanera WJ and Park AL. Association Between MRI Exposure During Pregnancy and Fetal and Childhood Outcomes. Jama. 2016; 316: 952-61.

4. Priego G, Barrowman NJ, Hurteaumiller J and Miller E. Does 3T Fetal MRI Improve Image Resolution of Normal Brain Structures between 20 and 24 Weeks' Gestational Age? American Journal of Neuroradiology. 2017; 38.

5. Bonel H, Frei KA, Raio L, Meyer-Wittkopf M, Remonda L and Wiest R. Prospective navigator-echo-based real-time triggering of fetal head movement for the reduction of artifacts. European Radiology. 2008; 18: 822-9.

6. Noise: a hazard for the fetus and newborn. American Academy of Pediatrics. Committee on Environmental Health. Pediatrics. 1997; 100: 724-7.

Figures

Table1 Magnetic resonance imaging protocols and scanning parameters

Table2 Sequence noise comparison between two groups

Table 3 Levels of image quality obtained in 20 patients in two groups

Fig1A: A coronal image was selected from each scan at the level of the third ventricle. One-millimeter ROIs were drawn in the developing brain layers: 1) germinal matrix, 2) periventricular, 3) subplate, and 4) cortical plate.

Fig1B: The qualitative results of two groups.

Fig1C-F: The ratio between signal intensity and air at each location for two groups.


Proc. Intl. Soc. Mag. Reson. Med. 27 (2019)
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