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AJR 2004; 183:79-81
© American Roentgen Ray Society


Technical Innovation

Retrospective Respiration-Gated MDCT: Initial Results in Canine Models

Kazuo Awai1, Daisuke Utsunomiya1, Masanori Imuta1, Shinya Shiraishi1, Yasuyuki Yamashita1, Yasumasa Nishimura2, Natsuko Sato3 and Maiko Kudo3

1 Department of Diagnostic Radiology, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjyo, Kumamoto 860-8556, Japan.
2 Department of Radiology, Kinki University School of Medicine, 377-2 Oono-higashi, Osaka-Sayama City 589-8511, Japan.
3 Philips Medical Systems, Tokyo 108-8507, Japan.

Received November 19, 2003; accepted after revision February 4, 2004.

 
Address correspondence to K. Awai.


Introduction
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Introduction
Materials and Methods
Results
Discussion
References
 
In the field of cardiac CT, development of retrospective ECG-gated MDCT has made it possible to observe cardiac motion in three dimensions [1], and use of CT coronary arteriography has become increasingly common because it provides excellent spatial resolution. Like the heart beat, respiratory motion is a periodic motion, and thus retrospective respiration-gated MDCT is theoretically possible. In healthy persons, however, the respiratory rate (20–25 breaths per minute) is markedly lower than heart rate (60–80 beats per minute). Therefore, retrospective respiration-gated MDCT would require an extremely small helical pitch value (≤ 0.2). An added complication is that, unlike the motion of the heart, much of the motion in the lungs is in the craniocaudal direction.

The purpose of our study was to verify whether it is possible to observe respiration using retrospective respiration-gated MDCT in dogs.


Materials and Methods
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Introduction
Materials and Methods
Results
Discussion
References
 
The experiment was conducted in three beagle dogs, each weighing approximately 11 kg. First, we placed the dogs under general anesthesia by administering 25 mg/kg of pentobarbital sodium via a 20-gauge IV catheter inserted into the radial vein of the right forelimb. After tracheal intubation, the animals were placed in a supine position on the CT table. We then administered 1 mL of 0.2% suxamethonium to bring spontaneous breathing to a standstill and connected a respirator to the intubation tube to provide artificial respiration at a rate of 30 breaths per minute. The tidal volume was set at 30 mL for two dogs and 35 mL for one dog.

CT was performed with 16-MDCT scanner (Mx8000/IDT16, Philips Medical Systems). The scanning parameters were as follows: detector configuration, 0.75 mm x 16; slice thickness, 0.8 mm; rotation time, 0.42 sec; helical pitch, 0.2; display field of view, 25 cm; 120 kV; 65 mAs (effective tube current, 30 mAs); and scanning range, 18 cm.

Because a respiration-gating unit was not available, we connected an ECG signal simulator to the ECG-gating unit of the MDCT scanner to achieve respiration gating. The ECG signal simulator generated signals for 30 breaths per minute, in accordance with respiratory rate of each dog.

Axial images obtained in 10 respiratory phases were reconstructed on the operator console of the scanner by dividing the 2,000 msec respiratory cycle into 10 phases using the MDCT cardiac reconstruction algorithm. Both the slice thickness and interval of the axial images were 0.8 mm. The axial image data were transferred to a workstation (Virtual Place Advance, version 2.0, Medical Imaging Laboratory). Coronal and sagittal images in each respiratory phase were then generated on the workstation, also with a slice thickness and interval of 0.8 mm. Finally, coronal and sagittal maximum-intensity-projection (MIP) images with a slab thickness of 10 mm were generated from original coronal and sagittal images.

We viewed the data set of MIP images obtained during all respiratory phases in the coronal and sagittal planes using cine mode on the workstation. We evaluated artifacts on the original axial images and on the coronal and sagittal MIP images in all respiratory phases. Furthermore, we evaluated the motion of the peripheral pulmonary vessels by comparing the relative length to the relative width of the adjacent intercostal space in the coronal and sagittal MIP images. We defined peripheral pulmonary vessels as vessels located within the area of the thoracic wall. An index of radiation exposure during CT examination, the CT dose index, was calculated for the previously described scanning conditions.


Results
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Introduction
Materials and Methods
Results
Discussion
References
 
No conspicuous artifacts were seen in the images of respiratory motion obtained with a tidal volume of 30 mL in two dogs and with a tidal volume of 35 mL in one dog. On coronal images, the periphery of the pulmonary vessels moved by approximately one intercostal space around the lung base, whereas the pulmonary vessels hardly moved in relation to the ribs at the lung apex (Fig. 1A, 1B, 1C, 1D). No difference in the evaluations of the images was found between the two radiologists. The CT dose index was 4.3 mGy during scanning.



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Fig. 1A. Retrospective respiration-gated MDCT scans of canine lungs. Axial scans were obtained at level of right and left ventricles during tidal inspiration (A) and tidal expiration (B) phases.

 


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Fig. 1B. Retrospective respiration-gated MDCT scans of canine lungs. Axial scans were obtained at level of right and left ventricles during tidal inspiration (A) and tidal expiration (B) phases.

 


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Fig. 1C. Retrospective respiration-gated MDCT scans of canine lungs. Coronal maximum-intensity-projection images were obtained at level of right and left ventricles during tidal inspiration (C) and tidal expiration (D) phases. Right costophrenic angle moved from level of ninth rib (arrow, C) to level of 10th rib (arrow, D) between tidal inspiration and tidal expiration.

 


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Fig. 1D. Retrospective respiration-gated MDCT scans of canine lungs. Coronal maximum-intensity-projection images were obtained at level of right and left ventricles during tidal inspiration (C) and tidal expiration (D) phases. Right costophrenic angle moved from level of ninth rib (arrow, C) to level of 10th rib (arrow, D) between tidal inspiration and tidal expiration.

 


Discussion
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Introduction
Materials and Methods
Results
Discussion
References
 
Clinical Applications
This study confirmed that retrospective respiration-gated MDCT is possible and is a promising method for future analysis of respiratory motion. The technique has clinical applications in the following five areas.

Assessment of the chest wall and mediastinal invasion by lung cancer.—Some authors have reported using CT scans of respiratory motion to assess the chest wall and mediastinal invasion by tumor [2, 3]. However, these authors used methods that required rescanning the lesion after routine scanning of both entire lungs. Our method makes it possible to obtain both conventional CT images and respirationgated images with one scan. In addition, our method makes it easy to observe the craniocaudal motion of the lungs by constructing coronal and sagittal views. MRI assessment of the chest wall and mediastinal invasion by lung cancer has been reported [4], but CT allows the lesion to be analyzed more closely because of its much higher spatial resolution.

Observation of diaphragmatic motion in advanced pulmonary emphysema.—Volume reduction surgery such as resection of bulla and emphysematous lungs is frequently performed in patients with bullous emphysema to improve respiratory motion. In these patients, diaphragmatic motion is often observed on MRI as an index of respiratory motion [5]. However, lesion distribution in the lungs must also be examined on CT because MRI cannot visualize the lungs themselves. We can observe diaphragmatic motion and lesion distribution in the lungs at the same time on retrospective respiration-gated dynamic MDCT.

Diagnosis of airway diseases.—In patients with airway diseases, we can use retrospective respiration-gated dynamic MDCT to prove air trapping by comparing the reconstructed images obtained during the expiratory phase with those obtained during the inspiratory phase.

Radiotherapy for lung cancer.—Retrospective respiration-gated dynamic MDCT makes it possible to capture 3D images of a tumor as respiration causes it to move and thus could allow accurate targeting of the tumor for irradiation.

Routine CT of patients who are unable to breath-hold.—Reconstructing images obtained during the maximal inspiration phase is sufficient for establishing a diagnosis in patients who cannot breath-hold. However, our method cannot be adapted for patients who have severe respiratory conditions that cause difficulties in regular breathing.

Radiation Dose
The CT dose index was 4.3 mGy during our examination. In our CT scanner, CT dose index is equivalent at any helical pitch with the same tube voltage (kV) and tube current (mAs per slice). With the scanning parameters of 120 kV and 200 mAs per slice, the CT dose index is estimated to be 13.3 mGy for both routine chest CT performed with a helical pitch of 1.2 and retrospective respirationgated MDCT performed with helical pitch of 0.2 or less. Therefore, using retrospective respiration-gated MDCT in place of routine CT of the chest is valid.

Conclusion
Retrospective respiration-gated MDCT is feasible, and its possible clinical applications are promising.


References
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Introduction
Materials and Methods
Results
Discussion
References
 

  1. Ohnesorge B, Flohr T, Becker C, et al. Cardiac imaging by means of electrocardiographically gated multisection spiral CT: initial experience. Radiology2000; 217:564 –571[Abstract/Free Full Text]
  2. Murata K, Takahashi M, Mori M, et al. Chest wall and mediastinal invasion by lung cancer: evaluation with multisection expiratory dynamic CT. Radiology1994; 191:251 –255[Abstract/Free Full Text]
  3. Shirakawa T, Fukuda K, Miyamoto Y, Tanabe H, Tada S. Parietal pleural invasion of lung masses: evaluation with CT performed during deep inspiration and expiration. Radiology1994; 192:809 –811[Abstract/Free Full Text]
  4. Sakai S, Murayama S, Murakami J, Hashiguchi N, Masuda K. Bronchogenic carcinoma invasion of the chest wall: evaluation with dynamic cine MRI during breathing. J Comput Assist Tomogr1997; 21:595 –600[Medline]
  5. Gierada DS, Hakimian S, Slone RM, Yusen RD. MR analysis of lung volume and thoracic dimensions in patients with emphysema before and after lung volume reduction surgery. AJR1998; 170:707 –714[Abstract/Free Full Text]

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