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Change in renal blood flow in response to intrarenal pressure alterations induced by ureteroscopy in an in-vivo porcine model

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Abstract

Introduction

High irrigation rates are commonly used during ureteroscopy and can increase intrarenal pressure (IRP) substantially. Concerns have been raised that elevated IRP may diminish renal blood flow (RBF) and perfusion of the kidney. Our objective was to investigate the real-time changes in RBF while increasing IRP during Ureteroscopy (URS) in an in-vivo porcine model.

Methods

Four renal units in two porcine subjects were used in this study, three experimental units and one control. For the experimental units, RBF was measured by placing an ultrasonic flow cuff around the renal artery, while performing ureteroscopy in the same kidney using a prototype ureteroscope with a pressure sensor at its tip. Irrigation was cycled between two rates to achieve targeted IRPs of 30 mmHg and 100 mmHg. A control data set was obtained by placing the ultrasonic flow cuff on the contralateral renal artery while performing ipsilateral URS.

Results

At high IRP, RBF was reduced in all three experimental trials by 10–20% but not in the control trial. The percentage change in RBF due to alteration in IRP was internally consistent in each porcine renal unit and independent of slower systemic variation in RBF encountered in both the experimental and control units.

Conclusion

RBF decreased 10–20% when IRP was increased from 30 to 100 mmHg during ureteroscopy in an in-vivo porcine model. While this reduction in RBF is unlikely to have an appreciable effect on tissue oxygenation, it may impact heat-sink capacity in vulnerable regions of the kidney.

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Data availability

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

References

  1. Sierra A, Corrales M, Kolvatzis M, et al: Real Time Intrarenal Pressure Control during Flexible Ureterorrenscopy Using a Vascular PressureWire: Pilot Study. J. Clin. Med. Res. 2022; 12. Available at: https://doi.org/10.3390/jcm12010147.

  2. Jung H, Osther PJS (2015) Intraluminal pressure profiles during flexible ureterorenoscopy. Springerplus 4:373

    Article  PubMed  PubMed Central  Google Scholar 

  3. Patel RM, Jefferson FA, Owyong M et al (2021) Characterization of intracalyceal pressure during ureteroscopy. World J Urol 39:883–889

    Article  PubMed  Google Scholar 

  4. Thomsen HS, Dorph S, Olsen S (1981) Pyelorenal backflow in normal and ischemic rabbit kidneys. Invest Radiol 16:206–214

    Article  CAS  PubMed  Google Scholar 

  5. Thomsen HS, Dorph S, Olsen S (1982) Pyelorenal backflow in rabbits following clamping of the renal vein and artery: radiologic and microscopic investigation. Acta Radiol Diagn 23:143–148

    Article  CAS  Google Scholar 

  6. Hinman F, Redewill FH (1926) PYELOVENOUS BACK FLOW. JAMA 87:1287–1293

    Article  Google Scholar 

  7. Boccafoschi C, Lugnani F (1985) Intrarenal reflux. Urol Res 13:253–258

    Article  CAS  PubMed  Google Scholar 

  8. Stenberg A, Bohman SO, Morsing P et al (1988) Back-leak of pelvic urine to the bloodstream. Acta Physiol Scand 134:223–234

    Article  CAS  PubMed  Google Scholar 

  9. Thomsen HS, Larsen S and Talner LB: Pyelorenal backflow during retrograde pyelography in normal and ischemic porcine kidneys. A radiologic and pathoanatomic study. Eur. Urol. 1982; 8: 291–297.

  10. Kottooran C, Twum-Ampofo J, Lee J et al (2023) Evaluation of fluid absorption during flexible ureteroscopy in an in-vivo porcine model. BJU Int 131:213–218

    Article  PubMed  Google Scholar 

  11. Pedersen KV, Liao D, Osther SS et al (2012) Distension of the renal pelvis in kidney stone patients: sensory and biomechanical responses. Urol Res 40:305–316

    Article  PubMed  Google Scholar 

  12. Zhong W, Leto G, Wang L et al (2015) Systemic inflammatory response syndrome after flexible ureteroscopic lithotripsy: a study of risk factors. J Endourol 29:25–28

    Article  PubMed  Google Scholar 

  13. Kreydin EI, Eisner BH (2013) Risk factors for sepsis after percutaneous renal stone surgery. Nat Rev Urol 10:598–605

    Article  PubMed  Google Scholar 

  14. Hvistendahl JJ, Pedersen TS, Jørgensen HH et al (1996) Renal hemodynamic response to gradated ureter obstruction in the pig. Nephron 74:168–174

    Article  CAS  PubMed  Google Scholar 

  15. Balawender K: A Prospective Study of Renal Blood Flow during Retrograde Intrarenal Surgery. J. Clin. Med. Res. 2023; 12. Available at: https://doi.org/10.3390/jcm12083030.

  16. Yazici CM, Akgul M, Ozcaglayan O et al (2021) Prospective Evaluation of Ipsilateral and Contralateral Renal Blood Flow During Retrograde Intrarenal Surgery. Urology 154:77–82

    Article  PubMed  Google Scholar 

  17. Dumbill R, Mellati A, Yang BD et al (2023) Ureterorenoscopy during normothermic machine perfusion: effect of varying renal pelvis pressure. BJU Int 131:50–52

    Article  PubMed  Google Scholar 

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

    PubMed  Google Scholar 

  19. Dalal R, Bruss ZS, Sehdev JS (2022) Physiology. StatPearls Publishing, Renal Blood Flow and Filtration

    Google Scholar 

  20. Ron Marom, Julie J. Dau, Timothy L. Hall, Khurshid R. Ghani, William W. Roberts: In-Vivo Thermal Tissue Mapping in a Porcine Model During Laser Activation. In: Engineering and Urology Society, 36th Annual Meeting. 2023.

  21. Kalantarinia K, Belcik JT, Patrie JT et al (2009) Real-time measurement of renal blood flow in healthy subjects using contrast-enhanced ultrasound. Am J Physiol Renal Physiol 297:F1129–F1134

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Glenny RW, Bernard S, Brinkley M (1993) Validation of fluorescent-labeled microspheres for measurement of regional organ perfusion. J Appl Physiol 74:2585–2597

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

The authors would like to acknowledge Professor J. Brian Fowlkes for loaning us the transonic flow measurement system.

Funding

Funding for this research was provided through a research grant from Boston Scientific.

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Authors and Affiliations

Authors

Contributions

RM: project development, data collection, manuscript writing, and data analysis. WWR: manuscript writing/editing, data analysis, critical revision, and study management. JJD: manuscript editing. KRG: manuscript editing. TLH: manuscript editing.

Corresponding author

Correspondence to Ron Marom.

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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. 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.

Ethics 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).

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Marom, R., Dau, J.J., Ghani, K.R. et al. Change in renal blood flow in response to intrarenal pressure alterations induced by ureteroscopy in an in-vivo porcine model. World J Urol 41, 3181–3185 (2023). https://doi.org/10.1007/s00345-023-04641-3

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  • DOI: https://doi.org/10.1007/s00345-023-04641-3

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