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Logo of jastBioMed Centralthis articlesearchsubmit a manuscriptregisterJournal of Animal Science and Technology
 
J Anim Sci Technol. 2017; 59: 5.
Published online 2017 March 1. doi:  10.1186/s40781-017-0129-5
PMCID: PMC5331717

Thoracoscopy as a safe and effective technique for exploring calves affected with bovine respiratory disease

Abstract

Background

Bovine respiratory disease (BRD) is one of the leading causes of economic losses in the beef and dairy industry. Reliable antemortem tools for diagnosing BRD would improve the efficacy of treatment and reduce costs. Here we examined whether the relatively simple technique of thoracoscopy can support BRD diagnosis under field conditions. We also compared various equipment set-ups in order to optimize the safety and efficacy of the procedure. A total of 24 thoracoscopic procedures were performed in 17 calves diagnosed with BRD and in 2 healthy control calves. Rigid and flexible endoscopes and industrial videoscopes were tested using various insertion approaches. The suitability of the technique was assessed in terms of duration, volume of air extracted, visualization score, and image quality. Safety was assessed in terms of rectal temperature, body weight, breaths/min, presence of fibrinogen, pain score, recovery time, intraoperative complications and risk of laceration or threatening collapse.

Results

Insertion of a flexible endoscope via a right, dorso-caudal approach at the 5th intercostal space allowed complete examination of the right lung in 15 min, as well as identification of main lung lesions and adherences in calves with BRD, without compromising calf welfare. While the dorso-caudal approach was optimal, it was associated with substantial discomfort when rigid endoscopes were used, minimal complications or mortality due to thoracoscopy were observed up to 28 days after the procedure. Videoscopes were as safe and easy to use as endoscopes, but endoscopes provided better image quality.

Conclusion

This study provides the first field evidence that thoracoscopy can be safe to explore BRD-diseased calves. These results justify a larger study to rigorously assess the diagnostic performance of the technique.

Keywords: Thoracoscopy, Bovine Respiratory Disease, Calves, Suitability, Field conditions

Background

Bovine respiratory disease (BRD) is a major health issue in calves [17]. It is associated with greater rearing costs, higher risk of mortality and relapse, lower growth and early culling [8]. Post-mortem examination of lung lesions is a useful indicator of BRD prevalence [9], for which it shows specificity and sensitivity >75% [10]. Studies using this technique suggest that up to 17% of slaughtered calves in the Netherlands show extensive lung lesions [11]. However, post-mortem examination does not aid in the identification or treatment of currently affected animals [9], highlighting the need for reliable ante-mortem diagnostic tools that may improve both prognosis and treatment outcomes [12].

Ultrasonographic diagnosis of BRD in living animals is based on the sign of ‘lung consolidation’ [1317]. This sign is routinely used to assess subclinical BRD [15], and it remains the best tool available for analysis of living animals [14, 16], particularly in feedlots [18]. However, this technique has limitations [1921]. Researchers have raised concerns that diagnosis based on it may not always be reliable because internationally standardized ultrasound criteria for BRD are lacking [22]. In addition, ultrasound may be less reliable in the specific case of older feedlot calves, in which the presence and position of the squeeze chute and forelimb muscles can prevent clear imaging of the cranial part of the lung, which is the first lung tissue to be affected in BRD [23].

A complementary technique to ultrasound may be thoracoscopy, a minimally invasive, low-risk technique [24, 25] that allows assessment of intrathoracic processes. While images obtained by thoracoscopy can complement and support ultrasound images, the technique simultaneously allows the collection of tissue samples (biopsies), which have proven to be effective for diagnosing disease in other animal species [2628], such as equines [24, 27, 2931]. Thoracoscopy shows potential in cattle, based on two reports in healthy adult cows [25, 32] and one report in an adult cow with pericardiectomy [33]. It remains unclear whether thoracoscopy is effective on a larger scale and under field conditions.

The aim of the present study was to determine whether thoracoscopy in calves with BRD is safe and effective under field conditions. We also hoped to determine the optimal equipment and procedure to guide future research and implementation of this innovative method.

Methods

This study involved 10 Holstein and 9 cross-breed calves from commercial feedlots (body weight, 132.39 ± 76.82 kg), of which 17 were suffering from BRD based on the following criteria: previous episodes with body temperature ≥40 °C, at least two clinical signs of BRD (cough, purulent nasal discharge, dyspnea and/or polypnea), at least two previous unsuccessful antibiotic treatments and growth retardation or weight loss [34, 35]. The two calves without BRD served as healthy controls in the study to assess the safety of the technique. During Phase 2 of the study (see Study design below), one control calf was euthanized the day after thoracoscopy with the farmer’s consent because of reduced expected performance, due to a previous femur fracture. Another calf was euthanized 7 days after thoracoscopy when persistently BVD infection was confirmed.

Procedures were carried out at the Large Animal Hospital at the Veterinary Faculty of Complutense University (Madrid, Spain) or at the animals’ farms, as indicated in Methods. Procedures complied with the Spanish Policy for Animal Protection (RD 1201/05), which fulfills European Union Directive 86/609 on the protection of animals.

Endoscopes and industrial videoscopes

Four different equipment set-ups were used (Fig. 1):

  • Set-up 1: rigid endoscope (Storz, Tuttlingen, Germany) with a length of 1 m and diameter of 4 mm, and laparoscopy cannula (Terman-type, Germany) with an internal diameter of 5 mm.
  • Set-up 2: flexible bronchoscope (Storz), with a working channel, a diameter of 6 mm and a length of 1.5 m.
  • Set-up 3a: portable industrial videoscope (Panter F3000, Madrid, Spain) with low-quality imaging capability, 170° rotation capability, length of 1 m and diameter of 5 mm, and other characteristics similar to those of the flexible endoscope.
  • Set-up 3b: portable industrial videoscope (XL Vu Sensing & Inspection, GE, Naples, Italy) with high-quality imaging capability, 80° rotation capability, length of 1 m and diameter of 5 mm.

Fig. 1
Evaluation of different endoscope and videoscope equipment set-ups for performing thoracoscopies in calves chronically affected with BRD. Set-up 1 involves a rigid endoscope; set-up 2, a flexible endoscope; set-up 3a, an industrial videoscope with low-quality ...

The only adjustment required for visualization was manually optimizing the light intensity depending on the distance between the end of the endoscope and the lung tissue. In practice, this intensity was similar across all the set-ups.

Study design

Phase 1 (pilot testing of procedures on three calves in hospital)

Three Holstein calves with medical history of chronic BRD and clinical BRD at the time of the study, were hospitalized and monitored daily. A rigid endoscope was used to perform thoracoscopy once in all animals (set-up 1, Fig. 1). At 22 daysays after the first procedure, a second thoracoscopy was performed in all animals to determine whether the first thoracoscopy had caused any lesions. Two different approaches out of the three possible ones (dorso-caudal, medio-cranio-ventral or cranio-ventral; Fig. 2) were performed in each thoracoscopy, in the same calf. Therefore, Phase 1 involved 6 thoracoscopies and 8 approaches. Results were analyzed based only on the type of approach (dorso-caudal, medio-cranio-ventral or cranio-ventral), since the animals were assumed to be similar in their clinical and other characteristics.

Fig. 2
Evaluation of different approach areas for inserting the thoracoscope into calves chronically affected with BRD. X = recommended approach in the respective area; S = intercostal space in the recommended area. Intercostal ...

Phase 2 (18 procedures in 16 calves; 15 in feedlots and 3 in hospital)

As a result of our experiences during Phase 1, we decided to use only flexible equipment (set-ups 2, 3a and 3b; Fig. 1) in the dorsal approach (dorso-caudal at 5th intercostal space, Fig. 2). A total of 18 thoracoscopies were performed in 16 calves (7 Holstein and 9 crossbreed): 5 with a flexible endoscope (set-up 2), 9 with an industrial videoscope offering low image quality (set-up 3a) and 4 with an industrial videoscope offering high image quality (set-up 3b). All calves had a medical history of chronic BRD and clinical BRD at the time of thoracoscopy, except for two healthy calves that served as controls to assess the safety of the technique with these particular endoscopes. Three thoracoscopic procedures (one each with set-up 2, 3a or 3b) were performed under experimental conditions in hospitalized calves, while the other 15 thoracoscopies were performed under field conditions. Results were analyzed on the basis of set-up (1, 2, 3a or 3b) considering the approach as the experimental unit.

Thoracoscopy procedure

All procedures were performed on standing calves, except in two cases when the animals had to be recumbent because of prior injury. Animals were immobilized with a head halter and a chute. Meloxicam (Metacam, Boehringer Ingelheim Vetmedica, Ingelheim am Rhein, Germany) was delivered intravenously (0.5 mg/kg), and lidocaine 2% and adrenaline 2‰ (in 5 ml; Xilocaína, Laboratorios Ovejero S.A., León, Spain) were administered subcutaneously to the puncture area 15 min before the first incision. Sedation was unnecessary, except in four cases (4 of 19, 20%) when the animals were very temperamental (1 ml of 2% Xylazine, delivered intravenously; Rompun, Bayer Iberia S.L., Barcelona, Spain). Sedation was administered on the right side of the animal.

The surgical field was prepared by surgical scrubbing and shaving, then an incision 1 cm long was made parallel to the dorsum. A metal trocar was immediately introduced into the thoracic cavity to a depth of 3 cm without damaging lung parenchyma. Blunt dissection of the thoracic wall was performed by piercing the trocar through the intercostal muscles while rotating the trocar at the same time. This helped ensure that, after trocar removal, the muscle fibers would close the incision upon returning to their original position. The end of the cannula that did not penetrate into the thoracic cavity was covered with the finger of a gloved hand in order to prevent airflow into the cavity. The endoscope was then introduced through the cannula rapidly, after removing the finger from the end of the trocar, and the right cavity was explored. Intrathoracic air was withdrawn, when necessary, by manual extraction via a syringe attached to the end of the cannula (Fig. 3). After exploration, the cannula was removed and the skin incision sutured. In all procedures, image quality was sufficient, such that pneumothorax did not need to be induced.

Fig. 3
Handmade air evacuation system to reduce subclinical pneumothorax after thoracoscopy in calves chronically affected with BRD

Parameters and measurements

Studied parameters were evaluated by the same researcher in all cases. Parameters were classified into four categories (Table 1): “Animal”, “Technical”, “Safety” and “Diagnostic”. Lung and pleura lesions found in the BRD-lungs were classified as acute if the lung tissue area showed normal air volume surrounded by swollen tissue with a smooth surface and hyperemic color; or as chronic, if the lung area was pale and compressed, containing smaller air volume than normal [6, 36]. Severe adverse events, defined as any life-threatening event occurring during or soon after thoracoscopy, were recorded for up to 28 days after thoracoscopy by two veterinarians during daily visits.

Table 1
Description of variables evaluated during thoracoscopy of calves chronically affected with BRD

Data processing and descriptive statistics

Data were analyzed descriptively using SPSS 22 (IBM, New York, USA). Data for continuous variables were reported as arithmetic mean and standard deviation (SD); data for categorical variables, as frequency percentages; and data for ordinal variables, as median (range). Normality was assessed using the Shapiro-Wilk test, which is designed for small samples. Inter-group differences were assessed for significance using the non-parametric Kruskal-Wallis test; if the difference was associated with P < 0.05, it was further assessed using the Mann-Whitney test with Bonferroni post hoc adjustment. Differences in percentages were assessed with Chi-square tests.

Results

All thoracoscopies from both study phases were performed with minimal difficulty or adverse events. Results are summarized in Table 2.

Table 2
Experimentally determined parameters during thoracoscopy procedures in calves chronically affected with BRD

Phase 1

The three diseased animals examined in this phase suffered no peri- or postoperative adverse events, other than transitory polypnea during the procedure and light subcutaneous emphysema. Risk of threatening passive collapse was judged to be low in all cases (Table 2). All calves increased in body weight during the month after surgery, showing an average daily gain of 536 ± 206.15 g. Thoracoscopy did not increase plasmatic fibrinogen levels.

The thoracoscopy procedure lasted 8–23 min, though the first thoracoscopies in the first two animals took longer because two approaches were used per surgery. The volume of extracted air ranged from 1600 mL to 2100 mL in the first intervention, and from 0 to 1750 mL in the second procedure. None of the approaches led to a visualization score of “excellent”, while the ventral approach led to a score of “optimal” (Table 3).

Table 3
Experimentally determined technical and safety parameters for comparing different approaches used with rigid endoscopes (equipment set-up 1) during thoracoscopy of calves chronically affected with BRD

Animal discomfort was moderate in all cases except for one calf that experienced greater discomfort following the dorsal approach. Recovery time, defined as the time to eating, drinking and/or ruminating, was <1 h in all cases and <15 min after the second intervention. Risk of lung laceration was higher with the ventral approach and lower with the dorsal (Table 3).

When the procedure was repeated on the same three animals 22 days later, no evidence of complications or lesions attributable to the first procedure was observed, except for a small hyperemic area at the incision site of the first thoracoscopy in one animal (Fig. 4) and small fibrin remains on the thoracic wall in another animal.

Fig. 4
Thorascopic imaging and hyperemia in an area subjected to thoracoscopy 22 days before. The first and repeated thorascopies were performed using a rigid endoscope (equipment set-up 1). The calf was chronically affected with BRD

Phase 2

The collected experience during the first phase of the study indicated that the dorsal approach allowed simpler manipulations to achieve lung tissue exploration, including easier lung perforation (Table 3), but that this approach was associated with greater discomfort due to the rigidity of the equipment. Therefore, all thoracoscopies in Phase 2 were performed using flexible optics introduced via the dorsal approach (Fig. 2), with the exception of two cases in which the procedure was performed on recumbent animals. Extraction of intrathoracic air was considered unnecessary based on previous experience.

The score for breaths per minute was moderate in all interventions, which lasted 14.78 ± 3.84 min. The visualization score was “excellent”. Flexible endoscopes proved to be superior to industrial videoscopes because of their higher image quality description (Table 4).

Table 4
Experimentally determined technical and safety parameters for comparing different equipment set-ups during thoracoscopy of calves chronically affected with BRD

The Pain score was “slight” in 15 procedures. In 12 procedures, recovery time was <30 min. In one case, a light pleural laceration occurred in one calf because it was lying down during the thoracoscopy due to an old femur fracture. This calf was euthanized the day after thoracoscopy with the farmer’s consent. Another calf was euthanized 7 days after thoracoscopy when persistently BVD infection was confirmed. Risk of threatening passive collapse was judged to be low in all cases.

Since the study was not designed to prove the diagnostic power of the technique, only selected calves with a medical history of chronic BRD and two healthy calves were used. Different lung lesions were found in all BRD-affected calves, while no pneumonic lesions were observed in healthy animals (Figs. 2, ,55 and and6).6). Three animals presented small lung abscesses (Fig. 7) with patterns consistent with Mycoplasma bovis infection.

Fig. 5
Thoracoscopic imaging of BRD lesions using different equipment set-ups in calves chronically affected with BRD. Values refer to numbers of animals
Fig. 6
BRD lesions observed by thoracoscopy performed using different equipment set-ups. All images are of calves chronically affected with BRD. AC, acute lesion; CR, chronic lesion; ADH, adherence; ABS, abscess; ENP, emphysema; ED, edema; FIB, fibrin. Values ...
Fig. 7
Lung abscesses observed by thoracoscopy performed using a flexible endoscope (equipment set-up 2) in a calf chronically affected with BRD

Comparison of equipment set-ups

Set-up 1 (rigid) allowed more complete observation of cranial lobes when the endoscope was introduced via the ventral approach than via the dorsal approach, even though the dorsal approach was safer (P < 0.05, Table 3). The ventral approach was also associated with a lower pain score than the dorsal approach (3 vs. 4; P < 0.05, Table 3). On the other hand, the ventral approach did not allow complete visualization of the caudal lobe, and it was associated with high perforation risk (Table 3). In contrast, flexible optics (set-ups 2, 3a and 3b) introduced via the dorsal approach could enter safely between the cranial lobes, allowing close and peripheral visualization of lung tissue without compromising animal welfare. In fact, all intrathoracic structures could be examined after only one insertion of the optics, and flexible optics were more comfortable than rigid optics for most calves (P < 0.05, Table 4).

Set-up 1 provided images with an excellent image quality score (Table 2), making it superior to set-ups 3a and 3b, which involved industrial videoscopes with, respectively, low- and high-quality imaging capability. Nevertheless, the images obtained with set-up 1 were similar in quality to those obtained with flexible endoscopes (Table 4).

Discussion

The results of the present study support thoracoscopy as an amenable and safe potential diagnostic technique for BRD-affected calves under field conditions. Using flexible endoscopes (equipment set-up 2) inserted via the dorsal approach (Fig. 2) with standing animals, we were able to explore the right lung in approximately 15 min without compromising calf health or welfare. We were able to detect lesions in all of the 17 diseased calves in our study.

While clinical criteria alone may lead occasionally to misdiagnosis of chronic BRD, we were careful in our study to include only animals that had presented classic BRD symptoms demonstrated to be high specifically associated with BRD disease [35], associated to a delay in growth and weight in a continuous way for at least one month prior to our work [34].

While thoracoscopy has been used for decades in horses [37], studies of endoscopes in cows have appeared only recently [25, 32], and these involved rigid set-ups and standing healthy cows. The present study is, to our knowledge, the first to examine thoracoscopy in several diseased animals and to compare rigid and flexible equipment set-ups as well as different approaches under field conditions. We also systematically examined possible effects of the procedures on animal welfare and safety.

All calves increased in body weight during the month after surgery, showing an average daily gain of 536 ± 206.15 g. This is lower than the average daily gain of 1200 g reported for healthy feedlot mates living under similar conditions [38].

We found that the best combination was flexible equipment and the dorsal approach. Higher pain scores were observed when rigid equipment was used with the dorsal approach, although this procedure gave the highest visualization score. Higher pain scores were also observed when flexible equipment was used with the ventral approach.

Flexible endoscopes (equipment set-up 2) showed obvious advantages, as demonstrated in humans [39, 40]. With a flexible set-up, we were able to visualize the entire thoracic cavity relatively quickly with a single penetration, in contrast to the experiences reported when using rigid equipment for adult cows [25]. Image quality with the industrial videoscopes that we tested was not optimal. Nevertheless, their relatively low cost may make them attractive, and the real-time images may be adequate to detect BRD in advanced phases. However, they do not allow image recording, nor do they have the capability to take biopsies or remove adhesions.

An approach from the right-hand side was selected because necropsy studies indicate that right lung examination allows primary pulmonary disease diagnosis [29, 4143]. Since most animals with BRD present with bilateral lung lesions [44], we assumed that the right-hand side was representative of the overall lesion pattern. On the other hand, exploring only the right lung can miss up to 16% of lesions [42] or even 30% [16]. Further studies should investigate the optimal procedure for approaching the left lung when necessary. Regardless of which lung is explored, the cranial lobes should be examined completely, since they are the first areas to be affected in BRD and are among the worst-affected areas [42, 45].

All thoracoscopies were completed within 23 min, which is comparable to reports in cows (30 min [25], 20 min [32]) and horses (15 min [41]). Those previous studies were performed under controlled conditions in a hospital, whereas our study was performed under field conditions. Sedation may be necessary to ensure the safety of animals and operators when the animal is temperamental, which was the case with 4 of 19 animals in our study.

The adverse events most often associated with thoracoscopy include hemorrhage and trauma to adjacent structures within the thoracic cavity [46], mild subcutaneous emphysema and subclinical pneumothorax [41]. In our study, the only complication observed was minor transient subcutaneous emphysema. Laceration occurred in only one calf, which had to be recumbent during the procedure. This recumbent position impeded visualization of the cranial area, and the procedure was interrupted. We conclude, therefore, that thoracoscopy should be performed in standing animals, as described for horses [29, 41].

No calf in our study showed lung collapse. While passively introduced air was extracted in Phase 1 of the study, such extraction was deemed unnecessary in the 18 procedures of Phase 2. We did not need to infuse CO2 to improve visualization, in contrast to a previous study in cows [32], nor did we need to administer oxygen intranasally, in contrast to the report of a pericardiotomy in a cow [33]. Postsurgical antibiotherapy was unnecessary during our study, even though most of our procedures were performed under field conditions. In fact, no infectious complications were observed 28 days after surgery. No mortality was observed during the same period, except for two animals that were euthanized for humanitarian reasons. Another study also reported low mortality and complication rates after thoracoscopy in small animals [46].

We did not include post-mortem examination because we did not want to impact the productivity of the animals involved, which was necessary to gain the support of the farm owners involved. Therefore, the animals in our study were later fattened and slaughtered as per normal farm procedure. Future studies should verify our findings using post-mortem examination.

Although the present study was not designed to demonstrate diagnostic capability, our results show that thoracoscopy was able to detect several lesions (Figs. 5, ,6,6, ,77 and and8),8), supporting the potential usefulness of thoracoscopy as a complement to established techniques for diagnosing BRD. Thoracoscopy may be particularly useful because it allows sequential biopsying of live animals. In humans, thoracoscopy has been shown to enhance the sensitivity and specificity of lung biopsy-based diagnosis [47]. Thoracoscopy may facilitate studies based on sequential-biopsy lung mapping in order to clarify the disease process, support preclinical research and clinical trials, and perform pharmacovigilance. Therefore, this study establishes the feasibility and potential suitability of thoracoscopy for diagnosing calves infected with BRD. This justifies larger studies aimed at rigorously assessing the technique’s sensitivity and specificity.”

Fig. 8
Lung adhesions observed by thoracoscopy performed using a flexible endoscope (equipment set-up 2) in a calf chronically affected with BRD

Conclusions

Thoracoscopy has been demonstrated for the first time to be an easy, safe and rapid exploratory technique that could be applied under field conditions to animals affected by BRD.

Acknowledgments

We thank Pedro Cuesta and Iagoba Cano (Department of Research Support, Complutense University of Madrid) for help with statistical analyses. We thank all the owners of the explored animals and the staff of the Clinical Hospital for their work and help.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Availability of data and materials

Please contact author for data requests.

Authors’ contributions

NPV, IEC, JSP and SA performed the experimental work; NPV, SA and AGB designed the experiments, performed statistical analysis and wrote the manuscript; JVGM, AGB and SA contributed ideas, gave critical feedback during data analysis and revised the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

All authors read and approved the manuscript and gave their consent for publication.

Ethics approval

The owners of the explored animals gave their consent to participate in the present study.

Procedures were carried out at the Large Animal Hospital at the Veterinary Faculty of Complutense University (Madrid, Spain) or at the animals’ farms, as indicated in Methods. Procedures complied with the Spanish Policy for Animal Protection (RD 1201/05), which fulfills European Union Directive 86/609 on the protection of animals and the experimental protocol was evaluated by the Comité de Ética del Hospital Clínico Veterinario de la UCM de Madrid.

Contributor Information

Natividad Perez-Villalobos, moc.tevlairt@sobolallivpn.

Iñaki Espinosa-Crespo, se.oohay@opsercasonipsei.

José Sampayo-Cabrera, ten.xmg@c-e-c.

Juan-Vicente González-Martín, se.mcu.tev@ivnauj.

Antonio Gonzalez-Bulnes, se.aini@senlub.

Susana Astiz, Phone: +34 91 347 3769, se.aini@anasus.zitsa.

References

1. Loneragan G, Dargatz DA, Morley PS, Smith MA. Trends in mortality ratios among cattle in US feedlots. J Am Vet Med Assoc. 2001;219:1122–7. doi: 10.2460/javma.2001.219.1122. [PubMed] [Cross Ref]
2. Fulton RW. Bovine respiratory disease research (1983–2009) Anim Health Res Rev. 2009;10:131–9. doi: 10.1017/S146625230999017X. [PubMed] [Cross Ref]
3. Miles DG. Overview of the North American beef cattle industry and the incidence of bovine respiratory disease (BRD) Anim Health Res Rev. 2009;10:101–3. doi: 10.1017/S1466252309990090. [PubMed] [Cross Ref]
4. Patrick RL. A dairy producer’s view of respiratory disease. Anim Health Res Rev. 2009;10:111–2. doi: 10.1017/S1466252309990120. [PubMed] [Cross Ref]
5. Poulsen KP, McGuirk SM. Respiratory disease of the bovine neonate. Vet Clin North Am Food Anim Pract. 2009;25:121–37. doi: 10.1016/j.cvfa.2008.10.007. [PubMed] [Cross Ref]
6. Panciera RJ, Confer AW. Pathogenesis and pathology of bovine pneumonia. Vet Clin North Am Food Anim Pract. 2010;26:191–214. doi: 10.1016/j.cvfa.2010.04.001. [PubMed] [Cross Ref]
7. Woolums AR. Diseases of the respiratory system. In: Smith BP, editor. Large animal internal medicine. 5. St. Louis, Missouri: Elsevier; 2015. pp. 461–637.
8. Bach A. Associations between several aspects of heifer development and dairy cow survivability to second lactation. J Dairy Sci. 2011;94:1052–7. doi: 10.3168/jds.2010-3633. [PubMed] [Cross Ref]
9. Leruste H, Brscic M, Heutinck LFM, Visser EK, Wolthuis-Fillerup M, Bokkers EAM, Stockhofe-Zurwieden N, Cozzi G, Gottardo F, Lensink BJ, van Reenen CG. The relationship between clinical signs of respiratory system disorders and lung lesions at slaughter in veal calves. Prev Vet Med. 2012;105:93–100. doi: 10.1016/j.prevetmed.2012.01.015. [PubMed] [Cross Ref]
10. White BJ, Rente DG. Bayesian estimation of the performance of using clinical observations and harvest lung lesions for diagnosing bovine respiratory disease in post-weaned beef calves. J Vet Diagn Invest. 2009;21:446–53. doi: 10.1177/104063870902100405. [PubMed] [Cross Ref]
11. Van der Mei J, Van den Ingh TS. Lung and pleural lesions of veal calves at slaughter and their relationship with carcass weight. Vet Q. 1987;9:203–7. doi: 10.1080/01652176.1987.9694101. [PubMed] [Cross Ref]
12. Smith RA, Stokka GL, Radostits OM, Griffin DD. Health and production management in beef feedlots. In: Radostits O, editor. Herd health: food animal production. Philadelphia: WB Saunders; 2001. pp. 592–5.
13. Jung C, Bostedt H. Thoracic ultrasonography technique in newborn calves and description of normal and pathological findings. Vet Radiol Ultrasound. 2004;45:331–5. doi: 10.1111/j.1740-8261.2004.04063.x. [PubMed] [Cross Ref]
14. Olivett T, Burton AJ, Bicalho RC, Nydam DV. Use of rapid thoracic ultrasonography for detection of subclinical and clinical pneumonia in dairy calves. In: Proceedings of the American Association of Bovine Practitioners, Auburn, 2011. p. 148.
15. Buczinski S, Forté G, Bélanger AM. Short communication: Ultrasonographic assessment of the thorax as a fast technique to assess pulmonary lesions in dairy calves with bovine respiratory disease. J Dairy Sci. 2013;96:4523–8. doi: 10.3168/jds.2013-6577. [PubMed] [Cross Ref]
16. Buczinski S, Forté G, Francoz D, Bélanger AM. Comparison of thoracic auscultation, clinical score, and ultrasonography as indicators of bovine respiratory disease in preweaned dairy calves. J Vet Intern Med. 2014;28:234–42. doi: 10.1111/jvim.12251. [PMC free article] [PubMed] [Cross Ref]
17. Buczinski S, Ollivett L, Dendukuri TN. Bayesian estimation of the accuracy of the calf respiratory scoring chart and ultrasonography for the diagnosis of bovine respiratory disease in pre-weaned dairy calves. Prev Vet Med. 2015;119:227–31. doi: 10.1016/j.prevetmed.2015.02.018. [PubMed] [Cross Ref]
18. Rademacher RD, Buczinski S, Tripp HM. Systematic thoracic ultrasonography in acute bovine respiratory disease of feedlot steers: impact of lung consolidation on diagnosis and prognosis in a case–control study. Bov Pract. 2014;48:1–10.
19. Reinhold P, Smith HJ, Langenberg A, Lekeux P. Measurement of respiratory impedance in healthy calves using the impulse oscillation technique—Physiological and methodological aspects. Vet J. 1998;155:27–38. doi: 10.1016/S1090-0233(98)80032-4. [PubMed] [Cross Ref]
20. Babkine M, Blond L. Ultrasonography of the bovine respiratory system and its practical application. Vet Clin North Am Food Anim Pract. 2009;25:633–49. doi: 10.1016/j.cvfa.2009.07.001. [PubMed] [Cross Ref]
21. Ackermann MR, Derscheid R, Roth JA. Innate immunology of bovine respiratory disease. Vet Clin North Am Food Anim Pract. 2010;26:215–28. doi: 10.1016/j.cvfa.2010.03.001. [PMC free article] [PubMed] [Cross Ref]
22. Abutarbush S, Pollock CM, Wildman BK, Perrett T, Schunicht OC, Fenton RK, Hannon SJ, Vogstad AR, Jim GK, Booker CW. Evaluation of the diagnostic and prognostic utility of ultrasonography at first diagnosis of presumptive bovine respiratory disease. Can J Vet Res. 2012;76:23–32. [PMC free article] [PubMed]
23. Flöck M. Diagnostic ultrasonography in cattle with thoracic disease. Vet J. 2004;167:272–80. doi: 10.1016/S1090-0233(03)00110-2. [PubMed] [Cross Ref]
24. McCarthy TC. Diagnostic thoracoscopy. Clin Tech Small Anim Pract. 1999;14:213–9. doi: 10.1016/S1096-2867(99)80013-9. [PubMed] [Cross Ref]
25. Scharner D, Dorn K, Brehm W. Bovine thoracoscopy: Surgical technique and normal anatomy. Vet Surg. 2014;43:85–90. doi: 10.1111/j.1532-950X.2013.12086.x. [PubMed] [Cross Ref]
26. Ahmed N, Jones D. Video-assisted thoracic surgery: state of the art in trauma care. Injury. 2004;35:479–89. doi: 10.1016/S0020-1383(03)00289-4. [PubMed] [Cross Ref]
27. Lugo J, Peroni JF. Thoracoscopy and lung biopsy. In: McGorum BC, Dixon PM, Robinson NE, Schumacher J, editors. Equine respiratory medicine and surgery. Philadelphia: Elsevier; 2007. pp. 271–6.
28. Berchtold B, Meylan M, Gendron K, Morath U, Rytz U, Lejeune B. Successful treatment of an intrathoracic bronchogenic cyst in a Holstein-Friesian calf. Acta Vet Scand. 2013;55:14. doi: 10.1186/1751-0147-55-14. [PMC free article] [PubMed] [Cross Ref]
29. Vachon AM, Fischer AT. Thoracoscopy in the horse: diagnostic and therapeutic indications in 28 cases. Equine Vet J. 1998;30:467–75. doi: 10.1111/j.2042-3306.1998.tb04521.x. [PubMed] [Cross Ref]
30. Orsini JA. Chronicle of laser usage in equine surgery. J Equine Vet Sci. 2002;22:249–50. doi: 10.1053/jevs.2002.35609. [Cross Ref]
31. Peroni JF, Robinson NE, Stick JA, Derksen FJ. Pleuropulmonary and cardiovascular consequences of thoracoscopy performed in healthy standing horses. Equine Vet J. 2000;32:280–6. doi: 10.2746/042516400777032228. [PubMed] [Cross Ref]
32. Michaux H, Nichols S, Babkine M, Francoz D. Description of thoracoscopy and associated short-term cardiovascular and pulmonary effects in healthy cattle. Am J Vet Res. 2014;75:468–76. doi: 10.2460/ajvr.75.5.468. [PubMed] [Cross Ref]
33. Van Biervliet J, Kraus M, Woodie B, Divers TJ, Gelzer A, Ainsworth D. Thoracoscopic pericardiotomy as a palliative treatment in a cow with pericardial lymphoma. J Vet Cardiol. 2006;8:69–73. doi: 10.1016/j.jvc.2005.08.001. [PubMed] [Cross Ref]
34. Pardon B, Hostens M, Duchateau L, Dewulf J, De Bleecker K, Deprez P. Impact of respiratory disease, diarrhea, otitis and arthritis on mortality and carcass traits in white veal calves. BMC Vet Res. 2013;9:79. doi: 10.1186/1746-6148-9-79. [PMC free article] [PubMed] [Cross Ref]
35. Timsit E, Dendukuri N, Schiller I, Buczinski S. Diagnostic accuracy of clinical illness for bovine respiratory disease (BRD) diagnosis in beef cattle placed in feedlots: a systematic literature review and hierarchical Bayesian latent-class meta-analysis. Prev Vet Med. 2016;135:67–73. doi: 10.1016/j.prevetmed.2016.11.006. [PubMed] [Cross Ref]
36. Jubb KV, Kennedy PC. Patología de los animales domésticos. 3. Uruguay: Agropecuaria Hemisferio Sur; 1991.
37. Mackey VS, Wheat JD. Endoscopic examination of the equine thorax. Equine Vet J. 1985;17:140–2. doi: 10.1111/j.2042-3306.1985.tb02071.x. [PubMed] [Cross Ref]
38. González-Martín JV, Elvira L, Cerviño López M, Pérez Villalobos N, Calvo López-Guerrero E, Astiz S. Reducing antibiotic use: selective metaphylaxis with florfenicol in commercial feedlots. Livestock Sci. 2011;141:173–81. doi: 10.1016/j.livsci.2011.05.016. [Cross Ref]
39. Licht PB, Ladergaard L. Flexible thoracoscopy may facilitate video-assisted thoracoscopic lobectomy. World J Surg. 2010;34:1470–4. doi: 10.1007/s00268-010-0468-6. [PubMed] [Cross Ref]
40. Ibrahim M, D’Andrilli A, Ciccone AM, Maurizi G, Cassiano F, Rendina EA. Flexible videoscope for thoracoscopic lobectomy: evolution of uniportal technique. Surg Endosc. 2015;29:2056–9. doi: 10.1007/s00464-014-3865-3. [PubMed] [Cross Ref]
41. Peroni JF, Horner NT, Robinson NE, Stick JA. Equine thoracoscopy: normal anatomy and surgical technique. Equine Vet J. 2001;33:231–7. doi: 10.2746/042516401776249688. [PubMed] [Cross Ref]
42. Epperson WB. A Preliminary Assessment of Lung Lesion Distribution in Fed Cattle. In: Department of Animal Science of South Dakota State University, editor. Beef Report. South Dakota, USA: Brookings; 2003. p. 15.
43. Monnet E. Interventional Thoracoscopy in Small Animals. Vet Clin North Am Food Anim Pract. 2009;39:965–75. doi: 10.1016/j.cvsm.2009.05.005. [PubMed] [Cross Ref]
44. Andrews GA, Kennedy GA. Respiratory diagnostic pathology. Vet Clin North Am Food Anim Pract. 1997;13:515–47. doi: 10.1016/S0749-0720(15)30312-1. [PubMed] [Cross Ref]
45. Rezac DJ, Thomson DU, Siemens MG, Prouty FL, Reinhardt CD, Bartle SJ. A survey of gross pathologic conditions in cull cows at slaughter in the Great Lakes region of the United States. J Dairy Sci. 2014;97:4227–35. doi: 10.3168/jds.2013-7636. [PubMed] [Cross Ref]
46. Radlinsky MG. Complications and need for conversion from thoracoscopy to thoracotomy in small animals. Vet Clin North Am Small Anim Pract. 2009;39:977–84. doi: 10.1016/j.cvsm.2009.05.006. [PubMed] [Cross Ref]
47. Janssen JP. Why you do or do not need thoracoscopy. Eur Respir Rev. 2010;19:213–6. doi: 10.1183/09059180.00005410. [PubMed] [Cross Ref]

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