Analyze Diet
Frontiers in veterinary science2020; 7; 601326; doi: 10.3389/fvets.2020.601326

Changes in Arterial Blood Pressure and Oxygen Tension as a Result of Hoisting in Isoflurane Anesthetized Healthy Adult Horses.

Abstract: In anesthetized adult horses, changes in recumbency can influence the cardiovascular system but how arterial blood pressures and oxygen tension change in isoflurane anesthetized animals as a direct result of hoisting has not been investigated. To evaluate effects of hoisting on hemodynamic function and pulmonary gas exchange in isoflurane-anesthetized horses. Prospective, experimental study. Six adult horses were anesthetized three times using isoflurane in pure oxygen (inspired fraction 0.9-1.0), and allowed breathing spontaneously in lateral recumbency. After 45 min horses were hoisted using a single hoist-hobble system for 5 min and returned into left lateral recumbency. Heart rate (HR), respiratory rate (RR), and systolic (SAP), diastolic (DAP), and mean arterial blood pressures (MAP) were measured every minute starting from 5 min before to 5 min after hoisting. Arterial blood gas samples were collected before, during, and after hoisting. Significant changes in hemodynamic parameters and PaO but not PaCO were found between baseline recordings and measurements obtained during and early after hoisting. The MAP decreased within the 1st min of hoisting from a mean of 74 ± 17 mmHg at baseline to 57 ± 20 mmHg ( < 0.05). Thereafter, it rapidly recovered to baseline before continuing to rise to higher than baseline values and then remaining elevated for 5 min after horses were returned into lateral recumbency. Simultaneously, the HR increased by 6-9 beats per min during the initial 3 min of hoisting before returning close to baseline values ( < 0.05). The PaO decreased significantly from a mean of 324.9 ±137.0 mmHg at baseline to a mean of 141.3 ± 104.2 mmHg during hoisting ( < 0.001) without recovering any more to baseline values. Hoisting an adult horse during or at the end of isoflurane anesthesia carries the risk of a precipitous, though short-lived (1-2 min), drop in arterial blood pressures and a persistent decrease in arterial oxygenation. While in systemically healthy animals the observed functional impairments were not life-threatening, they may be more severe in systemically compromised horses.Therefore, arterial blood pressures and oxygenation must be carefully monitored when hoisting sick equine patients during or at the end of inhalant anesthesia.
Publication Date: 2020-11-25 PubMed ID: 33324704PubMed Central: PMC7723898DOI: 10.3389/fvets.2020.601326Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research investigates the effects of hoisting on the cardiovascular system and pulmonary gas exchange in horses under isoflurane anesthesia. It was found that hoisting a horse during or at the end of this type of anesthesia can cause a significant, though temporary, drop in arterial blood pressures and a lasting decrease in oxygen levels.

Study Design

  • This study was designed as a prospective, experimental trial involving six adult horses. Each horse was anesthetized three times using isoflurane in pure oxygen and allowed to breathe spontaneously in a lateral position.
  • After 45 minutes, the horses were hoisted using a single hoist-hobble system for 5 minutes and then returned to the left lateral position. During this period, the heart rate, respiratory rate, and various arterial blood pressures were recorded.
  • Arterial blood gas samples were collected before, during, and after hoisting to measure changes in the oxygen and carbon dioxide content in the blood.

Findings

  • The researchers found significant changes in hemodynamic parameters and oxygen concentration, but not carbon dioxide concentration, between baseline measurements and those taken during and immediately after hoisting.
  • Within the first minute of hoisting, mean arterial blood pressure dropped significantly from a baseline of 74 ± 17 mmHg to 57 ± 20 mmHg. However, this quickly returned to baseline levels before rising to higher values and then stabilizing at an elevated level for 5 minutes after the horses were returned to lateral recumbency.
  • The heart rate increased by 6-9 beats per minute during the initial 3 minutes of hoisting before returning to near baseline levels.
  • The oxygen tension in the blood decreased significantly from a baseline of 324.9 ±137.0 mmHg to a mean of 141.3 ± 104.2 mmHg during hoisting. Unlike the blood pressure, the oxygen tension did not recover to baseline levels.

Conclusion

  • The findings suggest that hoisting a horse during or at the end of isoflurane anesthesia can cause a significant, though short-lived, drop in blood pressure and a persistent decrease in blood oxygen levels.
  • While these changes were not life-threatening in healthy horses, they may lead to more severe complications in horses that are systemically compromised.
  • As a result, it is crucial to monitor arterial blood pressures and blood oxygen levels closely when hoisting equine patients during or at the end of inhalant anesthesia.

Cite This Article

APA
Cerullo M, Driessen B, Douglas H, Hopster K. (2020). Changes in Arterial Blood Pressure and Oxygen Tension as a Result of Hoisting in Isoflurane Anesthetized Healthy Adult Horses. Front Vet Sci, 7, 601326. https://doi.org/10.3389/fvets.2020.601326

Publication

ISSN: 2297-1769
NlmUniqueID: 101666658
Country: Switzerland
Language: English
Volume: 7
Pages: 601326
PII: 601326

Researcher Affiliations

Cerullo, Michelle
  • Department of Clinical Sciences, University of Pennsylvania, School of Veterinary Medicine, Kennett Square, PA, United States.
Driessen, Bernd
  • Department of Clinical Sciences, University of Pennsylvania, School of Veterinary Medicine, Kennett Square, PA, United States.
Douglas, Hope
  • Department of Clinical Sciences, University of Pennsylvania, School of Veterinary Medicine, Kennett Square, PA, United States.
Hopster, Klaus
  • Department of Clinical Sciences, University of Pennsylvania, School of Veterinary Medicine, Kennett Square, PA, United States.

References

This article includes 32 references
  1. Auckburally A, Nyman G. Review of hypoxaemia in anaesthetized horses: predisposing factors, consequences and management.. Vet Anaesth Analg 2017 May;44(3):397-408.
    doi: 10.1016/j.vaa.2016.06.001pubmed: 28385614google scholar: lookup
  2. Johnston GM, Eastment JK, Wood J, Taylor PM. The confidential enquiry into perioperative equine fatalities (CEPEF): mortality results of Phases 1 and 2.. Vet Anaesth Analg 2002 Oct;29(4):159-170.
  3. Blissitt KJ, Raisis AL, Adams VJ, Rogers KH, Henley WE, Young LE. The effects of halothane and isoflurane on cardiovascular function in dorsally recumbent horses undergoing surgery.. Vet Anaesth Analg 2008 May;35(3):208-19.
  4. Driessen B, Nann L, Benton R, Boston R. Differences in need for hemodynamic support in horses anesthetized with sevoflurane as compared to isoflurane.. Vet Anaesth Analg 2006 Nov;33(6):356-67.
  5. Dobson A, Gleed RD, Meyer RE, Stewart BJ. Changes in blood flow distribution in equine lungs induced by anaesthesia.. Q J Exp Physiol 1985 Apr;70(2):283-97.
  6. Gasthuys F, de Moor A, Parmentier D. Haemodynamic effects of change in position and respiration mode during a standard halothane anaesthesia in ponies.. Zentralbl Veterinarmed A 1991 Apr;38(3):203-11.
  7. Hall LW, Gillespie JR, Tyler WS. Alveolar-arterial oxygen tension differences in anaesthetized horses.. Br J Anaesth 1968 Aug;40(8):560-8.
    doi: 10.1093/bja/40.8.560pubmed: 4875426google scholar: lookup
  8. Gillespie JR, Tyler WS, Hall LW. Cardiopulmonary dysfunction in anesthetized, laterally recumbent horses.. Am J Vet Res 1969 Jan;30(1):61-72.
    pubmed: 5782568
  9. Hall LW. Cardiovascular and pulmonary effects of recumbency in two conscious ponies.. Equine Vet J 1984 Mar;16(2):89-92.
  10. Bardell D, Mosing M, Cripps PJ. Restoration of arterial oxygen tension in horses recovering from general anaesthesia.. Equine Vet J 2020 Mar;52(2):187-193.
    doi: 10.1111/evj.13142pubmed: 31216080google scholar: lookup
  11. McMurphy RM, Cribb PH. Alleviation of postanesthetic hypoxemia in the horse.. Can Vet J 1989 Jan;30(1):37-41.
    pmc: PMC1680984pubmed: 17423205
  12. Mason DE, Muir WW, Wade A. Arterial blood gas tensions in the horse during recovery from anesthesia.. J Am Vet Med Assoc 1987 Apr 15;190(8):989-94.
    pubmed: 3106274
  13. Braun C, Trim CM, Eggleston RB. Effects of changing body position on oxygenation and arterial blood pressures in foals anesthetized with guaifenesin, ketamine, and xylazine.. Vet Anaesth Analg 2009 Jan;36(1):18-24.
  14. Araos JD, Larenza MP, Boston RC, De Monte V, De Marzo C, Grasso S, Haskins SC, Crovace A, Staffieri F. Use of the oxygen content-based index, Fshunt, as an indicator of pulmonary venous admixture at various inspired oxygen fractions in anesthetized sheep.. Am J Vet Res 2012 Dec;73(12):2013-20.
    doi: 10.2460/ajvr.73.12.2013pubmed: 23176433google scholar: lookup
  15. Manohar M, Gustafson R, Goetz TE, Nganwa D. Systemic distribution of blood flow in ponies during 1.45%, 1.96%, and 2.39% end-tidal isoflurane-O2 anesthesia.. Am J Vet Res 1987 Oct;48(10):1504-10.
    pubmed: 3674561
  16. Truijen J, Bundgaard-Nielsen M, van Lieshout JJ. A definition of normovolaemia and consequences for cardiovascular control during orthostatic and environmental stress.. Eur J Appl Physiol 2010 May;109(2):141-57.
    doi: 10.1007/s00421-009-1346-5pmc: PMC2861179pubmed: 20052592google scholar: lookup
  17. Brosnan RJ. Inhaled anesthetics in horses.. Vet Clin North Am Equine Pract 2013 Apr;29(1):69-87.
    doi: 10.1016/j.cveq.2012.11.006pmc: PMC3601575pubmed: 23498046google scholar: lookup
  18. Abrahamsen E, Hellyer PW, Bednarski RM, Hubbell JA, Muir WW 3rd. Tourniquet-induced hypertension in a horse.. J Am Vet Med Assoc 1989 Feb 1;194(3):386-8.
    pubmed: 2917909
  19. Copland VS, Hildebrand SV, Hill T 3rd, Wong P, Brock N. Blood pressure response to tourniquet use in anesthetized horses.. J Am Vet Med Assoc 1989 Oct 15;195(8):1097-103.
    pubmed: 2808099
  20. Wright BD, Hildebrand SV. An evaluation of apnea or spontaneous ventilation in early recovery following mechanical ventilation in the anesthetized horse.. Vet Anaesth Analg 2001 Jan;28(1):26-33.
  21. Day TK, Gaynor JS, Muir WW 3rd, Bednarski RM, Mason DE. Blood gas values during intermittent positive pressure ventilation and spontaneous ventilation in 160 anesthetized horses positioned in lateral or dorsal recumbency.. Vet Surg 1995 May-Jun;24(3):266-76.
  22. Jarvis KA, Steffey EP, Tyler WS, Willits N, Woliner M. Pulmonary blood flow distribution in anesthetized ponies.. J Appl Physiol (1985) 1992 Mar;72(3):1173-8.
    pubmed: 1568972doi: 10.1152/jappl.1992.72.3.1173google scholar: lookup
  23. Steffey EP, Kelly AB, Woliner MJ. Time-related responses of spontaneously breathing, laterally recumbent horses to prolonged anesthesia with halothane.. Am J Vet Res 1987 Jun;48(6):952-7.
    pubmed: 3605811
  24. Rugh KS, Garner HE, Hatfield DG, Herrold D. Arterial oxygen and carbon dioxide tensions in conscious laterally recumbent ponies.. Equine Vet J 1984 May;16(3):185-8.
  25. Mosing M, Senior JM. Maintenance of equine anaesthesia over the last 50 years: Controlled inhalation of volatile anaesthetics and pulmonary ventilation.. Equine Vet J 2018 May;50(3):282-291.
    doi: 10.1111/evj.12793pubmed: 29239012google scholar: lookup
  26. Robinson NE, Sorenson PR. Collateral flow resistance and time constants in dog and horse lungs.. J Appl Physiol Respir Environ Exerc Physiol 1978 Jan;44(1):63-8.
    doi: 10.1152/jappl.1978.44.1.63pubmed: 627502google scholar: lookup
  27. Albarrati A, Zafar H, Alghadir AH, Anwer S. Effect of Upright and Slouched Sitting Postures on the Respiratory Muscle Strength in Healthy Young Males.. Biomed Res Int 2018;2018:3058970.
    doi: 10.1155/2018/3058970pmc: PMC5845520pubmed: 29682532google scholar: lookup
  28. Taylor AH, Seymour CJ. Effect of low inspired oxygen fraction on respiratory indices in mechanically ventilated horses anaesthetised with isoflurane and medetomidine constant rate infusion.. Vet J 2016 May;211:70-4.
    doi: 10.1016/j.tvjl.2016.02.011pubmed: 27012166google scholar: lookup
  29. Marntell S, Nyman G, Hedenstierna G. High inspired oxygen concentrations increase intrapulmonary shunt in anaesthetized horses.. Vet Anaesth Analg 2005 Nov;32(6):338-47.
  30. Hubbell JA, Aarnes TK, Bednarski RM, Lerche P, Muir WW. Effect of 50% and maximal inspired oxygen concentrations on respiratory variables in isoflurane-anesthetized horses.. BMC Vet Res 2011 Jun 3;7:23.
    doi: 10.1186/1746-6148-7-23pmc: PMC3133541pubmed: 21639886google scholar: lookup
  31. Hopster K, Hopster-Iversen C, Geburek F, Rohn K, Kästner SB. Temporal and concentration effects of isoflurane anaesthesia on intestinal tissue oxygenation and perfusion in horses.. Vet J 2015 Jul;205(1):62-8.
    doi: 10.1016/j.tvjl.2015.04.030pubmed: 25986133google scholar: lookup
  32. Sarkar M, Niranjan N, Banyal PK. Mechanisms of hypoxemia.. Lung India 2017 Jan-Feb;34(1):47-60.
    doi: 10.4103/0970-2113.197116pmc: PMC5234199pubmed: 28144061google scholar: lookup

Citations

This article has been cited 0 times.