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Prevalence of lung atelectasis in sedated dogs examined with computed tomography

Abstract

Background

Computed tomography (CT) scanning of the lung is known to be a valuable tool when investigating lung pathology of the dog. During CT-scan the dog needs to be immobilized and general anesthesia has historically been considered as gold standard although being a more expensive and time-consuming alternative to sedation. Today, modern high speed multidetector CT-scanners offer new possibilities for sedation as an alternative. Both anesthesia and sedation can cause lung atelectasis, and this can be problematic when reading the CT-images since it potentially can masque or mimic lung pathology leading to misdiagnosis. The objective of this prospective analytic study was to investigate the prevalence of lung atelectasis and changes in lung attenuation over time in dogs that receive intravenous sedation and positioned in sternal recumbency.

Results

20 dogs without known lung pathology underwent three consecutive CT-scans of the lung; the first scan was initiated as soon as the dog was sufficiently sedated, the second scan approximately 5 min after the first one and the last scan after the dog’s orthopaedic scan was completed. The dogs received intravenous sedation in a combination of dexmedetomidine and butorphanol and were kept positioned in a strict sternal recumbency during sedation and exam. Each lung lobe was individually examined in an axial plane and measurements of dorsal, ventral, and mean lung attenuation were made. Atelectasis or areas with poorly aerated lung tissue were not detected as all parts of the lobes were normally aerated at all three scans. A statistically significant increase in lung attenuation between the first and the second scan (P = 0.03) and between the first and the third scan (P = 0.0004) was seen in the ventral part of the lobes.

Conclusions

This study indicates that CT-examination of the lungs can be performed on sedated dogs that are kept in a sternal recumbency without development of atelectasis. It also suggests that there is an early correlation between time and increase in lung attenuation.

Background

Computed tomography (CT) scanning is known as a valuable tool when examining thoracic and pulmonary disease in dogs and cats and is considered gold standard for diagnosing several conditions [1,2,3,4]. Animals undergoing CT-scans generally need to be sedated or anesthetized in order to perform the exam, but this may increase the risk of developing an increase in lung attenuation and even lung atelectasis [5,6,7,8,9]. Lung atelectasis is defined as an value between − 100 to 100 Hounsfield units (HU) while increase in lung attenuation ranges between − 500 to − 101 HU [15].

Lung atelectasis can be problematic when interpreting the images for mainly two reasons: firstly, atelectasis may mask true pathology. Secondly, there is a risk of misinterpreting atelectasis as a pathological change in the lung parenchyma.

Although successful CT studies of awake animals have been done using positioning devices in cats where little or no development of lung atelectasis was seen, [3, 10], this is not applicable in every day practice, especially not in dogs with high stress levels. Previous CT´studies have evaluated how lung attenuation alters with different anesthesia protocols and recumbencies [6,7,8, 11,12,13]. Results point towards the fact that animals positioned in a lateral recumbency tend to be at a higher risk of developing atelectasis or increase in lung attenuation than animals positioned in a sternal recumbency [7, 13, 14]. These changes tend to develop rapidly after anesthesia is induced, and that once it occurs, it might not resolve although the animal is repositioned [7]. In one recent study [9], ten dogs receiving intravenous sedation were examined with CT scanning showing no atelectatic lung changes. This study also showed that approximately 13,1% of the dogs developed hypoinflated lung parenchyma of which 2,4 ± 1,2% had a lung attenuation greater than − 250 HU.

The aim of this study was to determine if dogs without known lung pathology that were sedated intravenously with a combination of dexmedetomidine and butorphanol and positioned in sternal recumbency develop lung atelectasis. Alteration of lung attenuation over time was also assessed.

Methods

Dog population

This study took place at Evidensia Animal Hospital Södra Djursjukhuset (“South Animal Hospital”), Stockholm, during the period August 2019 to August 2020. Dogs included in this study were selected from a larger group of dogs undergoing a CT examination for front limb orthopaedic disease. The specific group was selected because they receive sedation as a standard, and they are examined in a sternal position, which was two important criteria for this study. None of the dogs received any intravenous contrast medium as a part of their orthopaedic limb CT-exam.

Dogs with lung disease, signs of systemic infection or inflammation according to blood test results and clinical examination, brachycephalic breeds, and dogs with recently known trauma or with suspicion of neoplasia were excluded. All dogs underwent physical examination prior to the CT-scanning including cardiac and pulmonary auscultation, heart rate, respiratory rate, assessment of general condition, and examination of mucus membranes. Basic parameters such as age, breed and gender were obtained from the patients’ journal. Blood samples were collected at the day of the study and C-reactive protein (CRP) and complete blood count was analyzed. Animals with hematologic signs of systemic infection or inflammation were excluded.

Study design

All animals received an aseptically peripheral vein catheter placed into a cephalic vein before receiving any sedatives. Sedation was given intravenously using the following protocol: butorphanol (Butomidor vet® 10 mg/mL) 0.2–0.4 mg/kg in combination with dexmedetomidine (Dexdomitor® 5 mg/mL) 2.5–5 mcg/kg followed by sterile saline to flush the syringe. If additional sedation was needed, this was also administered intravenously. Sedatives were given directly prior to the first CT scan. The dog was positioned in sternal recumbency with front legs pulled forward, and head in between its front legs.

Three lung scans (Scan 1—3) were performed on each patient. Time zero was stated as the time of sedation. According to Fig. 1, Scan 1 was performed as soon as possible after the patient was sufficiently sedated and correctly positioned, Scan 2 as shown approximately 5 min later. The ordinary scan, meaning the designated orthopaedic scan of the patient, was then performed prior to the third delayed scan, Scan 3, which could vary in time depending on how long time the ordinary scan took. A protocol was used to note the time for all three scans (Table 2).

Fig. 1
figure 1

Flow chart showing the onset of the three different lung scans; Scan 1, Scan 2 and Scan 3. Time zero stated as the time of sedation

CT examination and interpretation

All dogs were scanned in the same scanner (Philips Ingenuity Core 128 powered by iPatient, scanner V4.1.7.10503, Philips Healthcare Netherland B.V, Veenpluis 4–6, 5684 PC Best, Netherlands) 128 slice. A standardized lung protocol was used with technical parameters as follows: slice thickness 1.0 mm, pitch 1.074, matrix 512, image field of view − 600 to 1600, lung reconstruction algorithm Y-Detail (YD), kV 100, mAs 182, rotation time 0,75. Window width and level could be adjusted between study animals. Scans were obtained in a cranial to caudal direction with the dog in a sternal position. The time required for doing a lung scan using the dedicated machine varies between 3 to 10 s depending on the dog’s size.

Images were viewed in a PACS working station using the same software program for measurements of all dogs (HOROS™ dicom viewer). All images were analyzed by a single observer (aspirant in the Swedish program for Specialist in Diagnostic Imaging) under supervision of a board-certified specialist (Dipl.ECVDI).

Each lung lobe: left cranial lobe pars cranialis (LCPCr) and pars caudalis (LCPCa), left caudal (LC) lobe, right cranial lobe (RCr), right middle lobe (RM), right caudal lobe (RCa) and the accessory lobe (LA) were individually examined at all three scans. An axial slice where the most ventral tip of the lobe was included, was chosen and images from the three scans were compared and propagated so that measurements were done at the same topographic level on all time intervals. If the dog was repositioned between the lung scans, anatomical landmarks such as vertebrae, bronchi and vessels were used to examine the lobe at the same level. Care was taken that the most ventral tip of the lung lobe was included in the slice since lung atelectasis was expected to develop at this level first [15].

Three measurements of lung attenuation measured in HU were collected for each lobe (Fig. 2). First, a mean attenuation for each lung lobe was determined by manually drawing out the outlines of the lung lobe using a software tool included in HOROS™, excluding the main bronchi and aligned vessels. Second, a region of interest (ROI) of a minimum of 1 cm in diameter was manually drawn in the most dorsal part of the lung lobe. And third, a circle of ROI of a minimum of 1 cm in diameter, was drawn at the most ventral part of the lobe. Care was taken to avoid larger blood vessels and bronchi and the same anatomical areas were included in all of the three scans. If areas of visually increased attenuation could be seen these were also included using a free hand circle of ROI.

Fig. 2
figure 2

Axial slice showing how measurements were done in each lobe, in this image represented by the left caudal lung lobe. Lung attenuation was measured by placing a ROI of a minimum of 1 cm in the most dorsal and ventral part of the lung lobe, a mean was measured by drawing out the margins of the lung lobe using a free hand drawing tool

Lung attenuation was measured in HU and following values were used for interpreting the degree of lung attenuation: nonaerated (− 100 to + 100 HU) indicative of atelectasis, poorly aerated (− 500 to − 101 HU), normally aerated (−  900 to − 501 HU) or hyperaerated (− 1000 to − 901 HU) [12].

Statistical analyses

The statistical analyses were carried out in Matlab R 2020a.

To determine if there was a statistically significant increase in lung attenuation over time, a paired test “Signed rank Wilcoxon test” was used. For each individual, a mean of the ventral attenuation values of Scan 1 and scan 2 respectively Scan 1 and Scan 3 were compared.

Results

Animals

During the chosen period, 20 dogs that fit the inclusion criteria were examined (Table 1). All dogs recovered uneventfully from sedation.

Table 1 Basic data of study group including sex, breed and age

Clinical exam and blood sample

All dogs were clinically unapparent and without findings indicating systemic infection or inflammation, made by hematology and biochemistry.

Two dogs (Nos. 2 and 9) had a slight elevation in CRP 23.6 and 28.7 mg/L, respectively (reference interval 0–20 mg/L). In these dogs, there were no elevation of white blood count or signs of toxic neutrophils or left shift, and the dogs had normal clinical parameters.

Scan 1, 2 and 3

The different times for initiation of Scan 1,2 and 3 for each individual is presented in Table 2 with time zero stated as the time of sedation Fig. 2.

Table 2 The time noted for the three separate lung scans (Scan 1, Scan 2, Scan 3) for all 20 dogs, with time zero stated as the time of sedation

Technical data

The results showed that all measured areas of the lung parenchyma, both mean and the dorsal and ventral ROI-measurements were within the range of normally aerated lung parenchyma, defined as − 501 to − 900 HU (Fig. 3A–C). Hence, no atelectasis (− 100 to + 100 HU) or areas with poorly aerated lung tissue (− 500 to − 101 HU) were detected.

Fig. 3
figure 3

Lung attenuation in the ventral part of each lung lobe at Scan 1 (A), Scan 2 (B) and Scan 3 (C) measured in HU (y-scale). Values were obtained by drawing a circle of ROI in the ventral part of each lung lobe. Each colored dot represents an individual lung lobe for study dog 1–20 (x-scale)

Though all measurements were within the range of normally aerated lung tissue, a diversity within this spectrum could be seen. The highest mean quantitative measurement was found in the left cranial lobe pars caudalis (LCrPCa) with a value of − 569 obtained at the third scan (Scan 3) of dog nr 14. This third scan was also initiated last of all scans (24 min and 10 s after sedation). The highest quantitative focal measurement done with ROI was from the ventral part of the LCrPCa with a value of—571 HU obtained at the third scan (Scan 3) of dog no. 7. A motion artefact was noted from the same scan (Scan 3, dog no. 7) and this was the only motion artefact noticed.

Comparison of measurements between the different lung lobes at Scan 1, Scan 2 and Scan 3 is illustrated in Fig. 4, indicating an overall increase in lung attenuation over time. This association was further investigated with statistical analyses described below.

Fig. 4
figure 4

Mean value of ventral part of each lung lobe measured at Scan 1, Scan 2 and Scan 3

For each individual we computed the total lung attenuation as mean Hounsfield value across all lobes, as measured in the ventral part of the lobe (Fig. 5). A one-sided Wilcoxon signed rank test showed that the median total lung attenuation was significantly greater at scan 2 than at Scan 1 (P = 0.03), and greater at Scan 3 than at Scan 1 (P = 0.0004).

Fig. 5
figure 5

Mean lung attenuation as measured from the ventral part of all lobes for individual 1–20 at Scan 1, Scan 2 and Scan 3

Discussion

The aim of this study was to investigate if sedation was associated with lung atelectasis in dogs undergoing CT scanning. The findings show that neither atelectasis nor areas with poorly aerated lung tissue could be detected. These findings strengthens the results from a recent study done on sedated animals examined with CT [9], indicating that sedation alone is not a risk factor for lung atelectasis in healthy dogs. Also, compared to previous studies done on anesthetized animals, these results show lower frequency of alterations in lung attenuation [3, 8, 11, 14].

Although all measurements were within the range of normally aerated lung tissue, a statistically significant correlation between time and an increase in lung attenuation in the ventral part of the lung was observed. These changes developed rapidly between Scan 1 and Scan 2. These findings support previous studies in which alterations in lung attenuation developed rapidly, often within 3 to 8 min after anesthesia, and then remained relatively static over time [7,8,9]. The findings indicate that it is beneficial to initiate the patient’s CT scanning as soon as possible after sedation or anesthesia is induced to avoid an increased lung attenuation. In this study, all 20 dogs initiated their first scan within 7 min and 50 s after sedation and all scans were completed within a time span of up to 24 min and 10 s. This shows that if the patient and the staff are well prepared, it is possible to obtain a fast CT scanning of the lungs and still have time to perform additional scans such as contrast studies before any clinically significant increase in lung attenuation develop.

The highest mean quantitative attenuation measurement of a lobe was found in LCrPCa with a value of − 569 obtained at the third scan (Scan 3) from dog no. 14. This scan was initiated 24 min and 10 s after sedation, and this was also the one scan that was last initiated of all scans. The highest quantitative measurement obtained from a ROI, with a value of − 571 HU was made in dog no. 7 at the time of the 3rd scan. This was obtained from the ventral part of the left cranial lung lobe pars caudalis. The two measurements with the highest values were from the same lobe (LCrPCa) both obtained from the 3rd scan. These findings might indicate that there is an increased risk for increased lung attenuation in this lobe, potentially because of its small volume. Given the small number of animals used in this study, a statistically significant difference between lobes was not found.

Previous studies have shown that animals that are positioned in lateral recumbency are at risk of developing an increase in lung attenuation in the dependent lung lobe [7, 14, 15]. To avoid lateral or dorsal recumbency at any point and potentially resulting atelectasis, a fast intravenous administration method was chosen making it possible to support the animal in a sternal recumbency. For sedation, a combination of dexmedetomidine and butorphanol was used and injected intravenously with a rapid onset of sedation, making it possible to perform a first CT examination within a few minutes.

In anaesthetized animals the breathing can be controlled by using a breath holding technique [11] making it possible to avoid motion artifacts. When an animal is sedated using dexmedetomidine the respiratory rate is normally reduced [16] and this in combination with high scan speed in a modern multidetector CT scanner, provides the possibility to a large extent to avoid motion artefacts caused by breathing. Motion artefacts from breathing was only detected in one dog in one of the scans (Scan 3, dog no 7).

During the chosen period, 20 dogs that fit the inclusion criteria were included. Mainly young dogs are represented: 13/20 dogs were at the time of the study 1 year or younger and the oldest dog included was 8 years old. This is likely due to the high frequency of developmental orthopaedic disease affecting young individuals, as clinical indication for an orthopaedic CT exam was one of the inclusion criteria in the study.

This study was done on animals without clinical signs or any history of pulmonary disease where the described sedative protocol worked well. Due to this fact, it is possible that results from this study cannot be applicable on older animals or animals with lung disease where atelectasis might develop more easily.

A manual measuring method was chosen to determine the degree of lung attenuation by drawing the outlines of each lung lobe and also by using ventral and dorsal ROI. By using this method, all parts of the lung parenchyma independent of alterations in attenuation was included in the results. Since the HU-spectra for atelectasis, soft tissue and fat partly overlap, there could potentially be a risk of missing important areas of the lung parenchyma if a computerized method is used. When measuring the ventral and dorsal parts of the lung lobe, a ROI of a minimum of 1 cm in diameter was chosen. This was done in order to include an area large enough to minimize the alteration in attenuation caused by minor vessels and bronchi, but still be able to see focal differences between the dorsal and ventral parts of the lungs. In smaller dogs, this method was not optimal since the most ventral tip of the lobe was not included in the ventral measurements. Since this is the area where atelectasis could first arise, a mean attenuation including the tip of the lung was also obtained. Note should be taken that if a subjective increase in attenuation was seen, it would have been measured.

Measurements of lung attenuation was made in an axial plane in one representative slice for each lobe. It was not possible to standardize measurements to a certain lobe in relation to a certain vertebra because the individual variations between the study animals was too great leading to a subjective decision for where the most representative part of the lung was. When measuring a lobe at the three different time intervals, the images were linked to make sure that measurements were made in the same axial plane for the individual dog.

Conclusions

Intravenous sedation in combination with sternal recumbency provides excellent quality in CT images with low risk of developing lung atelectasis or attenuated lung tissue in dogs without known lung pathology, up to 24 min after sedation. The results also indicate that an increase in lung attenuation develop within minutes after sedation and that rapid sedation and initiation of scanning is therefore advantageous.

Availability of data and materials

The datasets generated and analyzed during the current study are not publicly available due to regulations under the General Data Protection Regulations, but parts of the data may be available from the corresponding author upon reasonable request.

References

  1. Prather AB, Berry CR, Thrall DE. Use of radiography in combination with computed tomography for the assessment of noncardiac thoracic disease in the dog and cat. Vet Radiol Ultrasound. 2005;46:114–21.

    Article  Google Scholar 

  2. Yoon J, Feeney DA, Cronk DE, Anderson KL, Ziegler LE. Computed tomographic evaluation of canine and feline mediastinal masses in 14 patients. Vet Radiol Ultrasound. 2004;45:542–6.

    Article  Google Scholar 

  3. Oliveira CR, Mitchell MA, O’Brien RT. Thoracic computed tomography in feline patients without use of chemical restraint. Vet Radiol Ultrasound. 2011;52:368–76.

    Article  Google Scholar 

  4. Armbrust LJ, Biller DS, Bamford A, Chun R, Garrett LD, Sanderson MW. Comparison of three-view thoracic radiography and computed tomography for detection of pulmonary nodules in dogs with neoplasia. J Am Vet Med Assoc. 2012;1(240):1088–94.

    Article  Google Scholar 

  5. Lamb CR, Jones ID. Associations between respiratory signs and abnormalities reported in thoracic CT scans of cats. J Small Anim Pract. 2016;1(57):561–7.

    Article  Google Scholar 

  6. Henao-Guerrero N, Ricco C, Jones JC, Buechner-Maxwell V, Daniel GB. Comparison of four ventilatory protocols for computed tomography of the thorax in healthy cats. Am J Vet Res. 2012;73:646–53.

    Article  Google Scholar 

  7. Foo TS, Pilton JL, Hall EJ, Martinez-Taboada F, Makara M. Effect of body position and time on quantitative computed tomographic measurements of lung volume and attenuation in healthy anesthetized cats. Am J Vet Res. 2018;79:874–83.

    Article  Google Scholar 

  8. Le Roux C, Cassel N, Fosgate GT, Zwingenberger AL, Kirberger RM. Computed tomographic findings of pulmonary atelectasis in healthy anesthetized beagles. Am J Vet Res. 2016;77:1082–92.

    Article  Google Scholar 

  9. Hunt TD, Wallack ST. Minimal atelectasis and poorly aerated lung on thoracic CT images of normal dogs acquired under sedation. Vet Radiol Ultrasound. 2021;1(62):647–56.

    Article  Google Scholar 

  10. Oliveira CR, Ranallo FN, Pijanowski GJ, Mitchell MA, Obrien MA, Mcmichael M, et al. The Vetmousetrap: a device for computed tomographic imaging of the thorax of awake cats. Vet Radiol Ultrasound. 2011;52:41–52.

    Article  Google Scholar 

  11. Guarracino A, Lacitignola L, Auriemma E, De Monte V, Grasso S, Crovace A, et al. Which airway pressure should be applied during breath-hold in dogs undergoing thoracic computed tomography? Vet Radiol Ultrasound. 2016;1(57):475–81.

    Article  Google Scholar 

  12. Staffieri F, Franchini D, Carella GL, Montanaro MG, Valentini V, Driessen B, et al. Computed tomographic analysis of the effects of two inspired oxygen concentrations on pulmonary aeration in anesthetized and mechanically ventilated dogs. Am J Vet Res. 2007;68:925–31.

    Article  Google Scholar 

  13. Lee SK, Park S, Cheon B, Moon S, Hong S, Cho H, et al. Effect of position and time held in that position on ground-glass opacity in computed tomography images of dogs. Am J Vet Res. 2017;1(78):279–88.

    Article  Google Scholar 

  14. Ahlberg N, Hoppe F, Kelter U, Svensson L. A computed tomographic study of volume and x-ray attenuation of the lungs of beagles in various body positions. Vet Radiol Ultrasound. 1985;26:43–7.

    Article  Google Scholar 

  15. Le Roux C, Cassel N, Fosgate GT, Zwingenberger AL, Kirberger RM. Computed tomographic findings of pulmonary atelectasis in healthy anesthetized beagles. Am J Vet Res. 2016;1(77):1082–92.

    Article  Google Scholar 

  16. FASS Vet. Dexmedetomidine [Internet]. https://www.fass.se/LIF/product;jsessionid=node0bqba38lokv2z1vva9ecaawlhg190635.node0?userType=1&nplId=20111018000068. Accessed 17 Mar 2020.

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Acknowledgements

A special thanks to dedicated nurses and veterinarians who helped us collect and care for study animals. Also, we would like to acknowledge Filip Malmberg Senior lecturer/Associate Professor at Department of Information Technology, Uppsala University for help with statistics.

Prior publication

Data have not been published previously.

Funding

Open access funding provided by IVC Evidensia AB. We would like to thank Marianne Thedes foundation for the financial assistance for carrying out this study.

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Authors and Affiliations

Authors

Contributions

All authors were involved in planning of the study. ER did all measurements from CT-scan images under supervision of FW. ER wrote the first drafts of the study but all authors contributed in the writing process. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Elin Reimegård, Helena T. Nyman Lee or Frida Westgren.

Ethics declarations

Ethics approval and consent to participate

The Swedish Board of Agriculture deemed that no ethical state research was needed for this study. All owners were informed about the study both orally and in text prior to the study and an owner consent was signed for all animals.

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Reimegård, E., Lee, H.T.N. & Westgren, F. Prevalence of lung atelectasis in sedated dogs examined with computed tomography. Acta Vet Scand 64, 25 (2022). https://0-doi-org.brum.beds.ac.uk/10.1186/s13028-022-00643-0

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Keywords

  • CT-scan
  • Intravenous sedation
  • Lung attenuation
  • Sternal recumbency