Utilizing smartphone-based electrocardiography and thoracic radiography to evaluate cardiac function and morphology in geriatric Sika deer (Cervus nippon)

Hugo A. Gonzalez-Jassi Veterinary Services, Safari Game Search Foundation DBA Wildlife Safari, Winston, OR

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Nicole LeBlanc Carlson College of Veterinary Medicine, Oregon State University, Corvallis, OR

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Benjamin E. Alcantar Veterinary Services, Safari Game Search Foundation DBA Wildlife Safari, Winston, OR

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Rodrigo S. Garces Torres Veterinary Services, Safari Game Search Foundation DBA Wildlife Safari, Winston, OR

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Abstract

OBJECTIVE

To describe qualitative and quantitative cardiothoracic values in geriatric Sika deer (Cervus nippon) using digital radiography, 6-lead ECG (sECG), and smartphone-based ECG (aECG).

ANIMALS

10 healthy geriatric Sika deer (9 females and 1 male).

PROCEDURES

Deer were chemically immobilized, thoracic radiographs were obtained, and inhalant anesthesia was initiated. An sECG and aECG were simultaneously recorded for each animal using the same ECG specifications. Results were compared between devices.

RESULTS

Radiographically, no deer had any cardiopulmonary abnormalities. Median (range) values for the most important cardiac measurements were 170 (153–193) mm for cardiac height, 135 (122–146) mm for cardiac width, 9 (8–9) for vertebral heart score, and 99 (69–124) mm for cardiosternal contact. All deer had a normal sinus rhythm with no pathological arrhythmias noted. A significant difference between sECG and aECG was identified for minimum heart rate (49 vs 51 beats/min, respectively), P wave duration (0.05 vs 0.03 seconds), P wave amplitude (0.28 vs 0.10 mV), PR interval (0.15 vs 0.12 seconds), and QT interval (0.39 vs 0.30 seconds).

CLINICAL RELEVANCE

Thoracic radiographs were suitable to evaluate basic cardiothoracic morphology in Sika deer. The aECG was useful for assessing heart rate and rhythm but, compared with sECG, proved no substitute for evaluating duration and amplitude of ECG waveforms.

Abstract

OBJECTIVE

To describe qualitative and quantitative cardiothoracic values in geriatric Sika deer (Cervus nippon) using digital radiography, 6-lead ECG (sECG), and smartphone-based ECG (aECG).

ANIMALS

10 healthy geriatric Sika deer (9 females and 1 male).

PROCEDURES

Deer were chemically immobilized, thoracic radiographs were obtained, and inhalant anesthesia was initiated. An sECG and aECG were simultaneously recorded for each animal using the same ECG specifications. Results were compared between devices.

RESULTS

Radiographically, no deer had any cardiopulmonary abnormalities. Median (range) values for the most important cardiac measurements were 170 (153–193) mm for cardiac height, 135 (122–146) mm for cardiac width, 9 (8–9) for vertebral heart score, and 99 (69–124) mm for cardiosternal contact. All deer had a normal sinus rhythm with no pathological arrhythmias noted. A significant difference between sECG and aECG was identified for minimum heart rate (49 vs 51 beats/min, respectively), P wave duration (0.05 vs 0.03 seconds), P wave amplitude (0.28 vs 0.10 mV), PR interval (0.15 vs 0.12 seconds), and QT interval (0.39 vs 0.30 seconds).

CLINICAL RELEVANCE

Thoracic radiographs were suitable to evaluate basic cardiothoracic morphology in Sika deer. The aECG was useful for assessing heart rate and rhythm but, compared with sECG, proved no substitute for evaluating duration and amplitude of ECG waveforms.

Supplementary Materials

    • Supplementary Figure S1 (PDF 87 KB)

Contributor Notes

Corresponding author: Dr. Gonzalez-Jassi (hg7891@gmail.com)
  • 1.

    Krebs BL, Marrin D, Phelps M, Krol L, Watters JV. Managing aged animals in zoos to promote positive welfare: a review and future directions. Animals (Basel). 2018;8(7):222. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 2.

    Kohler IV, Preston SH, Bingaman L. Comparative mortality levels among selected species of captive animals. Demogr Res. 2006;15:413434. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 3.

    Mattoon JS, Gerros TC, Brimacombe M. Thoracic radiographic appearance in the normal llama. Vet Radiol Ultrasound. 2001;42(1):2837. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 4.

    Schumacher J, Snyder P, Citino SB, Bennett RA, Dvorak LA. Radiographic and electrocardiographic evaluation of cardiac morphology and function in captive cheetahs (Acinonyx jubatus). J Zoo Wildl Med. 2003;34(4):357363. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 5.

    Smith J, Ward J, Urbano T, Mueller M. Use of AliveCor Heart Monitor for heart rate and rhythm evaluation in dairy water buffalo calves (Bubalis bubalis). J Dairy Vet Anim. 2016;4(2):14. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 6.

    Yaw TJ, Kraus MS, Ginsburg A, Clayton LA, Hadfield CA, Gelzer AR. Comparison of a smartphone-based electrocardiogram device with a standard six-lead electrocardiogram in the Atlantic bottlenose dolphin (Tursiops truncatus). J Zoo Wildl Med. 2018;49(3):689695. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 7.

    Santamarina G, Espino L, Suarez ML. Electrocardiographic parameters of free-ranging roe deer (Capreolus capreolus). J Zoo Wildl Med. 2001;32(4):441446. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 8.

    Sudhakara Reddy B, Sivajothi S. Electrocardiographic parameters of normal dairy cows during different ages. J Veter Sci Med. 2016;4(1):14. https://avensonline.org/wp-content/uploads/JVSM-2325–4645–04–0023.pdf.

    • Search Google Scholar
    • Export Citation
  • 9.

    Babicsak VR, Alves LS, Tsunemi MH, Vulcano LC. Radiographic measurements related with the cardiac size in young female Bergamasca sheep. Pesqui Vet Bras. 2017;37(12):15261530. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10.

    Nelson NC, Mattoon JS, Anderson DE. Radiographic appearance of the thorax of clinically healthy normal alpaca crias. Am J Vet Res. 2011;72(11):14391448. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 11.

    Buchanan JW, Bücheler J. Vertebral scale system to measure canine heart size in radiographs. J Am Vet Med Assoc. 1995;206(2):194199. https://pubmed.ncbi.nlm.nih.gov/7751220/.

    • Search Google Scholar
    • Export Citation
  • 12.

    Smith J, Heller M, Smith F, et al. Use of an AliveCor Heart Monitor for heart rate and rhythm evaluation in domestic goats. In: Proceedings of the American College of Veterinary Internal Medicine Research Forum. American College of Veterinary Internal Medicine; 2016;30:1516.

    • Search Google Scholar
    • Export Citation
  • 13.

    Makungu M. Thoracic radiographic anatomy in sheep. In: Proceedings of the Tanzania Veterinary Association. Tanzania Veterinary Association; 2017;32:129135.

    • Search Google Scholar
    • Export Citation
  • 14.

    Ryu S, Yamamoto S, Andersen CR, Nakazawa K, Miyake F, James TN. Intramural Purkinje cell network of sheep ventricles as the terminal pathway of conduction system. Anat Rec (Hoboken). 2009;292(1):1222. .

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 15.

    Ansari A, Yen Ho S, Anderson RH. Distribution of the Purkinje fibers in the sheep heart. Anat Rec. 1999;254(1):9297.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 16.

    Smith CR, Hamlin RL, Crocker HD. Comparative electrocardiography. Ann N Y Acad Sci. 1965;127(1):155169.

  • 17.

    Chalmeh A, Aktar IS, Zarei MH, Badkoubeh M. Electrocardiographic indices of clinically healthy Chios sheep. Vet Sci Dev. 2015;5(2):99102. .

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