Arjun Guduguntla
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Arjun Guduguntla has a total of 39 co-authors. Here are the top co-authors by number of shared publications:
- Abdullah Al-Khanaty
Department of Urology, Austin Health, Heidelberg, VIC 3084, Australia
1 shared publication - Abdullah Al-Khanaty
Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia
1 shared publication Andrew Ryan
Biomedicine Discovery Institute, Monash University, Melbourne, Victoria, Australia
1 shared publicationAndrew Xu
Department of Urology, Northern Health, Victoria, Australia
1 shared publication- Andrew Xu
Department of Medicine, Dentistry and Health Sciences University of Melbourne Melbourne VIC Australia
1 shared publication - Anthony Ta
Department of Urology, Austin Health, 145 Studley Road, Heidelberg, VIC 3084, Australia
1 shared publication
Latest Publications
- 24 April 2026
- Published by BMJ in BMJ Case Reports
- Vol. 19 (4) , e270197
Granulomatous prostatitis masquerading as suspected prostate cancer in a young patient on immunotherapy for psoriasis
We report a case of granulomatous prostatitis in a young male confirmed on histopathological examination. The case was initially presumed to be a case of prostate adenocarcinoma based on clinical, biochemical and imaging findings. To our knowledge, this is the second such reported case where there is a possible association between psoriasis and the subsequent development of granulomatous prostatitis and the only reported case of a patient on guselkumab immunotherapy.
- 24 April 2026
- Published by BMJ in BMJ Case Reports
- Vol. 19 (4) , e270197
Granulomatous prostatitis masquerading as suspected prostate cancer in a young patient on immunotherapy for psoriasis
We report a case of granulomatous prostatitis in a young male confirmed on histopathological examination. The case was initially presumed to be a case of prostate adenocarcinoma based on clinical, biochemical and imaging findings. To our knowledge, this is the second such reported case where there is a possible association between psoriasis and the subsequent development of granulomatous prostatitis and the only reported case of a patient on guselkumab immunotherapy.
- Open Access
Using Artificial Intelligence as a Risk Prediction Model in Patients with Equivocal Multiparametric Prostate MRI Findings
Introduction: PI-RADS 3 lesions represent a diagnostic grey zone on multiparametric MRI, with clinically significant prostate cancer (csPCa) detected in only 10–30%. Their equivocal nature leads to both unnecessary biopsies and missed cancers. Artificial intelligence (AI) has emerged as a potential tool to provide objective, reproducible risk prediction. This review summarises current evidence on AI for risk stratification in patients with indeterminate mpMRI findings, including clarification of key multicentre initiatives such as the PI-CAI (Prostate Imaging–Artificial Intelligence) study—a global benchmarking effort comparing AI systems against expert radiologists. Methods: A narrative review of PubMed and Embase (search updated to August 2025) was conducted using terms including “PI-RADS 3”, “radiomics”, “machine learning”, “deep learning”, and “artificial intelligence.” Eligible studies included those evaluating AI-based prediction of csPCa in PI-RADS 3 lesions using biopsy or long-term follow-up as reference standards. Both single-centre and multicentre studies were included, with emphasis on externally validated models. Results: Radiomics studies demonstrate that handcrafted features extracted from T2-weighted and diffusion-weighted imaging can distinguish benign tissue from csPCa, particularly in the transition zone, with area-under-the-ROC curves typically 0.75–0.82. Deep learning approaches—including convolutional neural networks and large-scale representation-learning frameworks—achieve higher performance and can reduce benign biopsy rates by 30–40%. Models that integrate imaging-based AI with clinical predictors such as PSA density further improve discrimination. The PI-CAI study, the largest international benchmark to date (>10,000 MRI exams), shows that state-of-the-art AI systems can match or exceed expert radiologists for csPCa detection across diverse scanners, centres, and populations, though prospective validation remains limited. Conclusions: AI shows strong potential to refine management of PI-RADS 3 lesions by reducing unnecessary biopsies, improving csPCa detection, and mitigating inter-reader variability. Translation into routine practice will require prospective multicentre validation, harmonised imaging protocols, and integration of AI outputs into clinical workflows with clear thresholds, decision support, and safety-net recommendations.
Open AccessUsing Artificial Intelligence as a Risk Prediction Model in Patients with Equivocal Multiparametric Prostate MRI Findings
Introduction: PI-RADS 3 lesions represent a diagnostic grey zone on multiparametric MRI, with clinically significant prostate cancer (csPCa) detected in only 10–30%. Their equivocal nature leads to both unnecessary biopsies and missed cancers. Artificial intelligence (AI) has emerged as a potential tool to provide objective, reproducible risk prediction. This review summarises current evidence on AI for risk stratification in patients with indeterminate mpMRI findings, including clarification of key multicentre initiatives such as the PI-CAI (Prostate Imaging–Artificial Intelligence) study—a global benchmarking effort comparing AI systems against expert radiologists. Methods: A narrative review of PubMed and Embase (search updated to August 2025) was conducted using terms including “PI-RADS 3”, “radiomics”, “machine learning”, “deep learning”, and “artificial intelligence.” Eligible studies included those evaluating AI-based prediction of csPCa in PI-RADS 3 lesions using biopsy or long-term follow-up as reference standards. Both single-centre and multicentre studies were included, with emphasis on externally validated models. Results: Radiomics studies demonstrate that handcrafted features extracted from T2-weighted and diffusion-weighted imaging can distinguish benign tissue from csPCa, particularly in the transition zone, with area-under-the-ROC curves typically 0.75–0.82. Deep learning approaches—including convolutional neural networks and large-scale representation-learning frameworks—achieve higher performance and can reduce benign biopsy rates by 30–40%. Models that integrate imaging-based AI with clinical predictors such as PSA density further improve discrimination. The PI-CAI study, the largest international benchmark to date (>10,000 MRI exams), shows that state-of-the-art AI systems can match or exceed expert radiologists for csPCa detection across diverse scanners, centres, and populations, though prospective validation remains limited. Conclusions: AI shows strong potential to refine management of PI-RADS 3 lesions by reducing unnecessary biopsies, improving csPCa detection, and mitigating inter-reader variability. Translation into routine practice will require prospective multicentre validation, harmonised imaging protocols, and integration of AI outputs into clinical workflows with clear thresholds, decision support, and safety-net recommendations.
- Open Access
- 18 December 2025
- Published by MDPI AG in Société Internationale d’Urologie Journal
- Vol. 6 (6) , 73
Cystolitholapaxy Without Transurethral Resection of the Prostate: Clinical Outcomes and Predictors of Subsequent Resection
Background/Objectives: Limited data exist on the outcomes of men with bladder stones undergoing cystolitholapaxy alone versus cystolitholapaxy with concurrent transurethral resection of the prostate (TURP). Additionally, factors associated with the need for subsequent TURP in these patients are not well defined. This study aimed to compare the clinical outcomes in men undergoing cystolitholapaxy alone with those undergoing concurrent cystolitholapaxy with TURP, and determine what factors were associated with the need for subsequent TURP. Methods: A retrospective review was conducted of men undergoing cystolitholapaxy at a single Australian hospital between 2014 and 2021. Patients were grouped into cystolitholapaxy alone (Group A) and cystolitholapaxy with concurrent TURP (Group B). Clinical outcomes compared included rates of acute urinary retention (AUR), urinary tract infection (UTI), and subsequent TURP. Prostate volume (PV), stone size, and the presence of intravesical prostatic protrusion (IPP) were evaluated as potential predictors of subsequent TURP in Group A. Results: Fifty men were included in the final analysis, with a median follow-up of 50 months (interquartile range [IQR] 24–81). Baseline characteristics did not differ significantly between groups. There was no statistically significant difference in the rates of AUR (11% vs. 13%) or UTI (22% vs. 30%) between Group A and Group B, respectively. However, 41% of Group A underwent subsequent TURP, compared to 9% in Group B (p = 0.0112). Within Group A, those requiring subsequent TURP had a significantly greater PV (65 vs. 34 cc, p = 0.0059), larger stone size (3.5 vs. 2.0 cm, p = 0.0175), and a higher prevalence of IPP (82% vs. 6%, p < 0.001). Conclusions: Cystolitholapaxy alone is a viable initial treatment for bladder stones, with comparable clinical outcomes to concurrent TURP. PV, stone size, and IPP may help identify patients likely to require future TURP, enabling more tailored treatment and potential reduction in TURP-related morbidity.
- 18 December 2025
- Published by MDPI AG in Société Internationale d’Urologie Journal
- Vol. 6 (6) , 73
Open AccessCystolitholapaxy Without Transurethral Resection of the Prostate: Clinical Outcomes and Predictors of Subsequent Resection
Background/Objectives: Limited data exist on the outcomes of men with bladder stones undergoing cystolitholapaxy alone versus cystolitholapaxy with concurrent transurethral resection of the prostate (TURP). Additionally, factors associated with the need for subsequent TURP in these patients are not well defined. This study aimed to compare the clinical outcomes in men undergoing cystolitholapaxy alone with those undergoing concurrent cystolitholapaxy with TURP, and determine what factors were associated with the need for subsequent TURP. Methods: A retrospective review was conducted of men undergoing cystolitholapaxy at a single Australian hospital between 2014 and 2021. Patients were grouped into cystolitholapaxy alone (Group A) and cystolitholapaxy with concurrent TURP (Group B). Clinical outcomes compared included rates of acute urinary retention (AUR), urinary tract infection (UTI), and subsequent TURP. Prostate volume (PV), stone size, and the presence of intravesical prostatic protrusion (IPP) were evaluated as potential predictors of subsequent TURP in Group A. Results: Fifty men were included in the final analysis, with a median follow-up of 50 months (interquartile range [IQR] 24–81). Baseline characteristics did not differ significantly between groups. There was no statistically significant difference in the rates of AUR (11% vs. 13%) or UTI (22% vs. 30%) between Group A and Group B, respectively. However, 41% of Group A underwent subsequent TURP, compared to 9% in Group B (p = 0.0112). Within Group A, those requiring subsequent TURP had a significantly greater PV (65 vs. 34 cc, p = 0.0059), larger stone size (3.5 vs. 2.0 cm, p = 0.0175), and a higher prevalence of IPP (82% vs. 6%, p < 0.001). Conclusions: Cystolitholapaxy alone is a viable initial treatment for bladder stones, with comparable clinical outcomes to concurrent TURP. PV, stone size, and IPP may help identify patients likely to require future TURP, enabling more tailored treatment and potential reduction in TURP-related morbidity.
- Open Access
- 12 August 2025
- Published by MDPI AG in Société Internationale d’Urologie Journal
- Vol. 6 (4) , 52
Trial of Void at Home After Green Light Laser Photosensitive Vaporisation of the Prostate: A Proof of Concept
Background/Objectives: Green light laser photosensitive vaporisation of the prostate (GLL-PVP) is a common procedure for bladder outlet obstruction, with a low incidence of post-operative bleeding. At Northern Health, postoperative management involved limited bladder washout with two bags of 2 L saline, spigotting, and undergoing a trial of void (TOV) the next morning. A new model of care was commenced in which patients were discharged after the two bags of washout, and the TOV occurred at home through the Hospital in the Home service. The aim of this study was to audit patient outcomes, patient satisfaction, and health service benefits of this novel program. Methods: Patients assigned to the program between March 2023 and June 2024 were analysed. Catheter removal occurred the morning after surgery, and the decision on the success of the TOV was made following an afternoon review. Results: A total of 93.3% (28/30) patients passed their TOV at home. There were no readmissions in the first 48 h postoperation, with only three emergency department (ED) presentations in this time. On a five-point rating scale, 25/25 questionnaire respondents were happy with their care, 20/25 rated the service as very good, and 5/25 rated the service as good. An extra AUD 3377.56 in revenue was generated per patient from the freed inpatient beds, which correlated to a net revenue of AUD 83,016.83 generated over the study period. Conclusions: At-home TOV after GLL-PVP is safe and feasible. There is high patient satisfaction and significant benefits to the healthcare system. This framework can additionally be adopted after other urological surgeries.
- 12 August 2025
- Published by MDPI AG in Société Internationale d’Urologie Journal
- Vol. 6 (4) , 52
Open AccessTrial of Void at Home After Green Light Laser Photosensitive Vaporisation of the Prostate: A Proof of Concept
Background/Objectives: Green light laser photosensitive vaporisation of the prostate (GLL-PVP) is a common procedure for bladder outlet obstruction, with a low incidence of post-operative bleeding. At Northern Health, postoperative management involved limited bladder washout with two bags of 2 L saline, spigotting, and undergoing a trial of void (TOV) the next morning. A new model of care was commenced in which patients were discharged after the two bags of washout, and the TOV occurred at home through the Hospital in the Home service. The aim of this study was to audit patient outcomes, patient satisfaction, and health service benefits of this novel program. Methods: Patients assigned to the program between March 2023 and June 2024 were analysed. Catheter removal occurred the morning after surgery, and the decision on the success of the TOV was made following an afternoon review. Results: A total of 93.3% (28/30) patients passed their TOV at home. There were no readmissions in the first 48 h postoperation, with only three emergency department (ED) presentations in this time. On a five-point rating scale, 25/25 questionnaire respondents were happy with their care, 20/25 rated the service as very good, and 5/25 rated the service as good. An extra AUD 3377.56 in revenue was generated per patient from the freed inpatient beds, which correlated to a net revenue of AUD 83,016.83 generated over the study period. Conclusions: At-home TOV after GLL-PVP is safe and feasible. There is high patient satisfaction and significant benefits to the healthcare system. This framework can additionally be adopted after other urological surgeries.
- Open Access
- 12 February 2025
- Published by MDPI AG in Société Internationale d’Urologie Journal
- Vol. 6 (1) , 5
A Review of the Intraoperative Use of Artificial Intelligence in Urologic Surgery
Introduction: Future evolutions of artificial intelligence (AI) will support autonomous surgery, conducted without the need for human decision making and implementation, but we have not yet achieved this level of technology. Presently, the predominant applications of AI in urological surgery are achieved using the tool of computer vision. This review aims to summarise potential intra-operative AI tools for urologists. Method: A systematic search was conducted through Scopus, PubMed, Embase, and Medline by two independent reviewers, with a third to resolve any conflicts. As a rule, only original articles describing the use or potential use of artificial intelligence intra-operatively in urologic surgery were included. A total of 60 articles were reviewed. Key content and findings: There is significant research investigating the ability to diagnose bladder tumours using AI assistance at the time of cystoscopy, with studies showing the ability to also grade tumour based on appearance and differentiate between carcinoma in situ and indeterminate lesions. With the aid of AI, kidney stones can accurately be identified and diagnosed morphologically intra-operatively. Various studies show the ability to overlay 2D and 3D anatomical models on a surgeon’s screen, as well as correctly identify important anatomical landmarks and surgical instruments, with AI support. All types of intra-operative data can be analysed with AI to assess surgeon performance, predict post-operative outcomes such as continence post prostatectomy, and recognise complications such as bleeding and ischemia. Conclusions: AI holds great potential for urologists during surgery to improve safety, diagnostic accuracy, identification of anatomical structures and surgical instruments, assessment of the surgeon for self-evaluation, and prediction of post-operative outcomes. Before the use of AI as an aid during surgery becomes standard practice, more prospective studies are needed to evaluate its real-world application, feasibility, and costs.
- 12 February 2025
- Published by MDPI AG in Société Internationale d’Urologie Journal
- Vol. 6 (1) , 5
Open AccessA Review of the Intraoperative Use of Artificial Intelligence in Urologic Surgery
Introduction: Future evolutions of artificial intelligence (AI) will support autonomous surgery, conducted without the need for human decision making and implementation, but we have not yet achieved this level of technology. Presently, the predominant applications of AI in urological surgery are achieved using the tool of computer vision. This review aims to summarise potential intra-operative AI tools for urologists. Method: A systematic search was conducted through Scopus, PubMed, Embase, and Medline by two independent reviewers, with a third to resolve any conflicts. As a rule, only original articles describing the use or potential use of artificial intelligence intra-operatively in urologic surgery were included. A total of 60 articles were reviewed. Key content and findings: There is significant research investigating the ability to diagnose bladder tumours using AI assistance at the time of cystoscopy, with studies showing the ability to also grade tumour based on appearance and differentiate between carcinoma in situ and indeterminate lesions. With the aid of AI, kidney stones can accurately be identified and diagnosed morphologically intra-operatively. Various studies show the ability to overlay 2D and 3D anatomical models on a surgeon’s screen, as well as correctly identify important anatomical landmarks and surgical instruments, with AI support. All types of intra-operative data can be analysed with AI to assess surgeon performance, predict post-operative outcomes such as continence post prostatectomy, and recognise complications such as bleeding and ischemia. Conclusions: AI holds great potential for urologists during surgery to improve safety, diagnostic accuracy, identification of anatomical structures and surgical instruments, assessment of the surgeon for self-evaluation, and prediction of post-operative outcomes. Before the use of AI as an aid during surgery becomes standard practice, more prospective studies are needed to evaluate its real-world application, feasibility, and costs.
- Open Access
- 15 January 2025
- Published by Wiley in BJUI Compass
- Vol. 6 (1) , e468
A novel bladder cancer surveillance schedule using bladder Cx for patients on annual surveillance
Objectives: Cx bladder monitor (CxM) is a urine test with a proven high sensitivity and negative predictive value in bladder cancer surveillance. The aim of this retrospective study was to report on the outcomes of our newly implemented bladder cancer surveillance program for patients eligible for yearly cystoscopy, as per the European Association of Urology (EAU) guidelines. In this program, eligible patients alternate between yearly surveillance cystoscopy and CxM, instead of the standard yearly surveillance cystoscopy. Outcomes measures were overall results of CxM and subsequent treatment patterns of patients, impact on waiting lists, cost comparison and patient satisfaction.Patients and Methods: In 2022, 109 eligible and consenting patients were identified, with 98 commencing on the new surveillance program, starting with CxM instead of cystoscopy. A negative CxM, would result in a planned flexible cystoscopy in 12 months. If a patient had a positive CxM, they proceeded to undergo a cystoscopy, and if required, imaging.Results: Of the 98 that underwent testing, 90 had a negative CxM test and 8 patients had a positive CxM test. Three of these eight were true positive (PPV 0.375). Seventy negative CxM patients had no recurrence at the time of the next cystoscopy/imaging. Of the remaining 20 negative CxM patients, 11 were found to have a recurrence at subsequent cystoscopy/imaging and 9 did not proceed with further surveillance for various reasons. All of the tumour recurrences diagnosed after a negative CxM were non‐invasive, thus there was no progression to muscle‐invasive disease. All suitable patients consented to continuing with the CxM protocol. The hospital surveillance cystoscopy waitlist was reduced by approximately 59% and CxM was approximately $850 AUD cheaper than a cystoscopy.Conclusion: CxM can be safely used in an alternating schedule with Flexible Cystoscopy for patients on annual bladder cancer surveillance.
- 15 January 2025
- Published by Wiley in BJUI Compass
- Vol. 6 (1) , e468
Open AccessA novel bladder cancer surveillance schedule using bladder Cx for patients on annual surveillance
Objectives: Cx bladder monitor (CxM) is a urine test with a proven high sensitivity and negative predictive value in bladder cancer surveillance. The aim of this retrospective study was to report on the outcomes of our newly implemented bladder cancer surveillance program for patients eligible for yearly cystoscopy, as per the European Association of Urology (EAU) guidelines. In this program, eligible patients alternate between yearly surveillance cystoscopy and CxM, instead of the standard yearly surveillance cystoscopy. Outcomes measures were overall results of CxM and subsequent treatment patterns of patients, impact on waiting lists, cost comparison and patient satisfaction.Patients and Methods: In 2022, 109 eligible and consenting patients were identified, with 98 commencing on the new surveillance program, starting with CxM instead of cystoscopy. A negative CxM, would result in a planned flexible cystoscopy in 12 months. If a patient had a positive CxM, they proceeded to undergo a cystoscopy, and if required, imaging.Results: Of the 98 that underwent testing, 90 had a negative CxM test and 8 patients had a positive CxM test. Three of these eight were true positive (PPV 0.375). Seventy negative CxM patients had no recurrence at the time of the next cystoscopy/imaging. Of the remaining 20 negative CxM patients, 11 were found to have a recurrence at subsequent cystoscopy/imaging and 9 did not proceed with further surveillance for various reasons. All of the tumour recurrences diagnosed after a negative CxM were non‐invasive, thus there was no progression to muscle‐invasive disease. All suitable patients consented to continuing with the CxM protocol. The hospital surveillance cystoscopy waitlist was reduced by approximately 59% and CxM was approximately $850 AUD cheaper than a cystoscopy.Conclusion: CxM can be safely used in an alternating schedule with Flexible Cystoscopy for patients on annual bladder cancer surveillance.
- 13 December 2024
- Published by Wiley in Anz Journal of Surgery
- Vol. 95 (1-2) , 117-123
NSQIP surgical risk calculator: a useful adjunct for the urology multidisciplinary meeting
Background: Surgical risk calculators are not often routinely used in Urology Multidisciplinary Meetings (MDM), and little is known about their impact on clinical decision‐making. The aim of this study is to assess the utility of the American College of Surgeons National Surgical Quality Improvement Program (NSQIP) risk calculator for decision‐making in the Urology MDM setting, with particular consideration given to decisions about surgical candidacy.Methods: We analysed all adult patients discussed in our Urology MDM with urological conditions whose management plan could potentially include major surgery. During a MDM, a consensus management decision was made prior to the NSQIP score being revealed to blinded team members. Any change in decision after revealing the score was documented, including rationale.Results: Sixty‐three out of 64 eligible cancer cases being discussed at MDM warranted NSQIP scores being revealed to the MDM post initial consensus. 95.2% (n = 60) did not have a change in the MDM management plan after reveal of NSQIP score. The NSQIP score led to a change in the MDM management decision in three cases: two renal cancer cases where management changed to biopsy with view to microwave ablation if positive, and one prostate cancer case, where management changed to recommend against radical prostatectomy.Conclusion: The NSQIP risk calculator was a useful tool and adjunct in the MDM setting. It served as a safety net where surgical risk was not initially properly estimated by team members, and reinforced decisions where there was concordance between NSQIP score and clinical judgement.
- 13 December 2024
- Published by Wiley in Anz Journal of Surgery
- Vol. 95 (1-2) , 117-123
NSQIP surgical risk calculator: a useful adjunct for the urology multidisciplinary meeting
Background: Surgical risk calculators are not often routinely used in Urology Multidisciplinary Meetings (MDM), and little is known about their impact on clinical decision‐making. The aim of this study is to assess the utility of the American College of Surgeons National Surgical Quality Improvement Program (NSQIP) risk calculator for decision‐making in the Urology MDM setting, with particular consideration given to decisions about surgical candidacy.Methods: We analysed all adult patients discussed in our Urology MDM with urological conditions whose management plan could potentially include major surgery. During a MDM, a consensus management decision was made prior to the NSQIP score being revealed to blinded team members. Any change in decision after revealing the score was documented, including rationale.Results: Sixty‐three out of 64 eligible cancer cases being discussed at MDM warranted NSQIP scores being revealed to the MDM post initial consensus. 95.2% (n = 60) did not have a change in the MDM management plan after reveal of NSQIP score. The NSQIP score led to a change in the MDM management decision in three cases: two renal cancer cases where management changed to biopsy with view to microwave ablation if positive, and one prostate cancer case, where management changed to recommend against radical prostatectomy.Conclusion: The NSQIP risk calculator was a useful tool and adjunct in the MDM setting. It served as a safety net where surgical risk was not initially properly estimated by team members, and reinforced decisions where there was concordance between NSQIP score and clinical judgement.
- Open Access
- 6 December 2024
- Published by Elsevier in Prostate International
- Vol. 13 (2) , 90-95
The addition of peri-operative gentamicin with ciprofloxacin reduces infection and sepsis rates post transrectal prostate biopsy
- 6 December 2024
- Published by Elsevier in Prostate International
- Vol. 13 (2) , 90-95
Open AccessThe addition of peri-operative gentamicin with ciprofloxacin reduces infection and sepsis rates post transrectal prostate biopsy