Skip to main content
Log in

Assessing renal tissue temperature changes and perfusion effects during laser activation in an in vivo porcine model

  • Original Article
  • Published:
World Journal of Urology Aims and scope Submit manuscript

Abstract

Introduction

High fluid temperatures have been seen in both in vitro and in vivo studies with laser lithotripsy, yet the thermal distribution within the renal parenchyma has not been well characterized. Additionally, the heat-sink effect of vascular perfusion remains uncertain. Our objectives were twofold: first, to measure renal tissue temperatures in response to laser activation in a calyx, and second, to assess the effect of vascular perfusion on renal tissue temperatures.

Methods

Ureteroscopy was performed in three porcine subjects with a prototype ureteroscope containing a temperature sensor at its tip. A needle with four thermocouples was introduced percutaneously into a kidney with ultrasound guidance to allow temperature measurement in the renal medulla and cortex. Three trials of laser activation (40W) for 60 s were conducted with an irrigation rate of 8 ml/min at room temperature in each subject. After euthanasia, three trials were repeated without vascular perfusion in each subject.

Results

Substantial temperature elevation was observed in the renal medulla with thermal dose in two of nine trials exceeding threshold for tissue injury. The temperature decay time (t½) of the non-perfused trials was longer than in the perfused trials. The ratio of t½ between them was greater in the cortex than the medulla.

Conclusion

High-power laser settings (40W) can induce potentially injurious temperatures in the in vivo porcine kidney, particularly in the medullary region adjacent to the collecting system. Additionally, the influence of vascular perfusion in mitigating thermal risk in this susceptible area appears to be limited.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Data availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

References

  1. Aldoukhi AH, Roberts WW, Hall TL et al (2017) Holmium laser lithotripsy in the new stone age: dust or bust? Front Surg 4:57

    Article  PubMed  PubMed Central  Google Scholar 

  2. Pietropaolo A, Mani M, Hughes T et al (2022) Role of low- versus high-power laser in the treatment of lower pole stones: prospective non-randomized outcomes from a university teaching hospital. Ther Adv Urol 14:17562872221097344

    Article  Google Scholar 

  3. Aldoukhi AH, Ghani KR, Hall TL et al (2017) Thermal response to high-power holmium laser lithotripsy. J Endourol 31(12):1308–1312

    Article  PubMed  Google Scholar 

  4. Aldoukhi AH, Hall TL, Ghani KR et al (2018) caliceal fluid temperature during high-power holmium laser lithotripsy in an in vivo porcine model. J Endourol 32(8):724–729

    Article  PubMed  PubMed Central  Google Scholar 

  5. Hein S, Petzold R, Schoenthaler M et al (2018) Thermal effects of Ho: YAG laser lithotripsy: real-time evaluation in an in vitro model. World J Urol 36(9):1469–1475

    Article  CAS  PubMed  Google Scholar 

  6. Maxwell AD, MacConaghy B, Harper JD et al (2019) Simulation of laser lithotripsy-induced heating in the urinary tract. J Endourol 33(2):113–119

    Article  PubMed  PubMed Central  Google Scholar 

  7. Wollin DA, Carlos EC, Tom WR et al (2018) Effect of laser settings and irrigation rates on ureteral temperature during holmium laser lithotripsy, an in vitro model. J Endourol 32(1):59–63

    Article  PubMed  Google Scholar 

  8. Hein S, Petzold R, Suarez-Ibarrola R et al (2020) Thermal effects of Ho:YAG laser lithotripsy during retrograde intrarenal surgery and percutaneous nephrolithotomy in an ex vivo porcine kidney model. World J Urol 38(3):753–760

    Article  PubMed  Google Scholar 

  9. Marom R, Dau JJ, Hall TL et al (2023) Thermal safety boundaries for laser power and irrigation rate during ureteroscopy: in-vivo porcine assessment with a Ho:YAG laser. Urology. https://doi.org/10.1016/j.urology.2023.07.014

    Article  PubMed  Google Scholar 

  10. Wang X-K, Jiang Z-Q, Tan J et al (2019) Thermal effect of holmium laser lithotripsy under ureteroscopy. Chin Med J 132(16):2004–2007

    Article  PubMed  PubMed Central  Google Scholar 

  11. U.S. Food & Drug Administration (FDA). Class 2 Device Recall Olympus. 2021. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=188172. Accessed 3 Jul 2023.

  12. Okhunov Z, Jiang P, Afyouni AS et al (2021) Caveat emptor: the heat is “ON”-an in vivo evaluation of the thulium fiber laser and temperature changes in the porcine kidney during dusting and fragmentation modes. J Endourol 35(11):1716–1722

    Article  PubMed  Google Scholar 

  13. Marom R, Dau JJ, Hall TL et al (2023) Effect of outflow resistance on intrarenal pressure at different irrigation rates during ureteroscopy: in vivo evaluation. Urolithiasis 51(1):98

    Article  PubMed  Google Scholar 

  14. Sapareto SA, Dewey WC (1984) Thermal dose determination in cancer therapy. Int J Radiat Oncol Biol Phys 10(6):787–800

    Article  CAS  PubMed  Google Scholar 

  15. Yarmolenko PS, Moon EJ, Landon C et al (2011) Thresholds for thermal damage to normal tissues: an update. Int J Hyperthermia 27(4):320–343

    Article  PubMed  PubMed Central  Google Scholar 

  16. Aldoukhi AH, Dau JJ, Majdalany SE et al (2021) Patterns of laser activation during ureteroscopic lithotripsy: effects on caliceal fluid temperature and thermal dose. J Endourol 35(8):1217–1222

    Article  PubMed  PubMed Central  Google Scholar 

  17. Louters MM, Dau JJ, Hall TL et al (2022) Laser operator duty cycle effect on temperature and thermal dose: in-vitro study. World J Urol 40(6):1575–1580

    Article  CAS  PubMed  Google Scholar 

  18. Dalal R, Bruss ZS, Sehdev JS (2022) Physiology, renal blood flow and filteration. StatPearls Publishing, Florida

    Google Scholar 

  19. Goldberg SN, Hahn PF, Tanabe KK et al (1998) Percutaneous radiofrequency tissue ablation: does perfusion-mediated tissue cooling limit coagulation necrosis? J Vasc Interv Radiol 9(1 Pt 1):101–111

    Article  CAS  PubMed  Google Scholar 

  20. Pallone TL, Edwards A, Mattson DL (2012) Renal medullary circulation. Compr Physiol 2(1):97–140

    Article  PubMed  Google Scholar 

Download references

Funding

Funding for this study was provided, in part, by a Faculty Catalyst Award, Department of Urology, University of Michigan, and, in part, by a research grant from Boston Scientific.

Author information

Authors and Affiliations

Authors

Contributions

R Marom: Project development, Data Collection, Manuscript writing, Data analysis. WW Roberts: Manuscript writing/editing, Data analysis, Critical Revision, Study management. JJ Dau: Manuscript editing. KR Ghani: Manuscript editing. TL Hall: Manuscript editing.

Corresponding author

Correspondence to Ron Marom.

Ethics declarations

Conflict of interest

K.R.G. has consulting relationships with Boston Scientific, Ambu, Olympus, Coloplast, and Karl Storz. W.W.R. has a consulting relationship with Boston Scientific. R.M., J.J.D., and T.L.H. have no disclosures.

Ethical approval

All procedures performed in the study involving animal subjects were in accordance with the ethical standards of the institutional research committee and were approved by the University of Michigan’s Institutional Animal Care and Use Committee (IACUC).

Disclaimer

The prototype ureteroscope used in this study was a concept device/technology, which was not available for sale at the time the study was conducted. Pre-clinical study results may not necessarily be indicative of clinical performance.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Marom, R., Dau, J.J., Ghani, K.R. et al. Assessing renal tissue temperature changes and perfusion effects during laser activation in an in vivo porcine model. World J Urol 42, 197 (2024). https://doi.org/10.1007/s00345-024-04896-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00345-024-04896-4

Keywords

Navigation