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The Use of a Virtual Reality Device (HypnoVR) During Extracorporeal Shockwave Lithotripsy for Treatment of Urinary Stones: Initial Results of a Clinical Protocol

Articolo
Data di Pubblicazione:
2023
Citazione:
The Use of a Virtual Reality Device (HypnoVR) During Extracorporeal Shockwave Lithotripsy for Treatment of Urinary Stones: Initial Results of a Clinical Protocol / Candela, L., Ventimiglia, E., Corrales, M., Sierra Del Rio, A., Villa, L., Goumas, I.K., Salonia, A., Montorsi, F., Doizi, S., Traxer, O.. - In: UROLOGY. - ISSN 1527-9995. - 175:(2023), pp. 13-17. [10.1016/j.urology.2023.01.048]
Abstract:
Objective: To assess the impact of a Virtual Reality Device (VRD, HypnoVR, Strasbourg, France) on patient-reported pain and anxiety during extracorporeal shockwave lithotripsy (ESWL). Materials and methods: We enrolled 30 patients submitted to ESWL for urinary stones. Patients with either epilepsy or migraine were excluded. ESWL procedures were performed using the same lithotripter (Lithoskop; Siemens, AG Healthcare, Munich, Germany) at a frequency of 1 Hz delivering 3000 shock waves per procedure. The VRD was installed and started 10 minutes before the procedure. Tolerability of pain and treatment-related anxiety represented the primary efficacy outcomes and were evaluated using: (1) a visual analogue scale (VAS), (2) the short version of the McGill pain questionnaire (MPQ), and (3) the short version of the surgical fear questionnaire (SFQ). Secondary outcomes were VRD ease of use and patient satisfaction. Results: Median (IQR) age was 57 (51-60) years and body mass index (BMI) was 23 (22-27) kg/m2. Median (IQR) stone size was 7 (6-12) mm with a median (IQR) density of 870 (800-1100) HU. Stone location was kidney in 22 (73%), and ureter in 8 (27%) patients. Median (IQR) extra time for installation was 6.5 (4-8) minutes. Overall, 20 (67%) patients were at their first ESWL treatment. Side effects were experienced by only 1 patient. Comprehensively, 28 (93%) patients would recommend and would use VRD again during ESWL. Conclusion: VRD application during ESWL is safe and feasible. The initial report from patients is positive in terms of pain and anxiety tolerance. Further comparative studies are needed.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Candela, Luigi; Ventimiglia, Eugenio; Corrales, Mariela; Sierra Del Rio, Alba; Villa, Luca; Goumas, Ioannis Kartalas; Salonia, Andrea; Montorsi, Francesco; Doizi, Steeve; Traxer, Olivier
Autori di Ateneo:
MONTORSI FRANCESCO
SALONIA ANDREA
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/145717
Pubblicato in:
UROLOGY
Journal
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https://www.sciencedirect.com/science/article/pii/S0090429523001437?via=ihub
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