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Surgical Management of Kidney and Ureteral Stones: AUA Guideline (2026)
Using AUA Guidelines
This AUA guideline is provided free of use to the general public for academic and research purposes. However, any person or company accessing AUA guidelines for promotional or commercial use must obtain a licensed copy. To obtain the licensable copy of this guideline, please contact Keith Price at kprice@auanet.org.
Unabridged version of this Guideline [pdf]
Algorithm for this Guideline [pdf]
To cite this guideline:
Pearle MS, Matlaga BR, Antonelli JA, et al. Surgical Management of Kidney and Ureteral Stones: AUA Guideline (2026) Part I: Evaluation and Treatment of Patients with Kidney and/or Ureteral Stones. J Urol. 0(0). doi:10.1097/JU.0000000000004842. Https://www.auajournals.org/doi/10.1097/JU.0000000000004842
Pearle MS, Matlaga BR, Antonelli JA, et al. Surgical Management of Kidney and Ureteral Stones: AUA Guideline (2026) Part II: Evaluation and Treatment of Patients with Kidney and/or Ureteral Stones. J Urol. 0(0). doi:10.1097/JU.0000000000004843. Https://www.auajournals.org/doi/10.1097/JU.0000000000004843
Pearle MS, Matlaga BR, Antonelli JA, et al. Surgical Management of Kidney and Ureteral Stones: AUA Guideline (2026) Part III: Evaluation and Treatment of Patients with Kidney and/or Ureteral Stones. J Urol. 0(0). doi:10.1097/JU.0000000000004844. Https://www.auajournals.org/doi/10.1097/JU.0000000000004844
Panel Members
Margaret S. Pearle, MD, PhD (co-chair); Brian R. Matlaga, MD, MPH (co-chair); Jodi A. Antonelli, MD; Thomas Chi, MD; Ryan S. Hsi, MD; Bodo Knudsen, MD; Kevin Koo, MD, MPH, MPhil; Naim M. Maalouf, MD; Vernon M. Pais Jr, MD, MS; Ann Paris, RN, JD; Kristina L. Penniston, PhD; Kymora B. Scotland, MD, PhD; Necole Streeper, MD; Gregory Tasian, MD, MSc, MSCE; Kyle D. Wood, MD; Justin B. Ziemba, MD, MSEd
Staff and Consultants
Sennett K. Kim; Erin Kirkby, MS; Lesley H. Souter, PhD
SUMMARY
PURPOSE
This Guideline covers the surgical management of patients with kidney and/or ureteral stones and is intended for clinicians evaluating and managing patients with this disease.
METHODOLOGY
This systematic review was conducted in two planned stages, including a search for systematic reviews followed by a search for primary literature.
OVID was used to systematically search MEDLINE and EMBASE databases for articles evaluating surgical management of kidney and ureteral stones. The Panel selected control articles that were deemed relevant and the articles were compared with the literature search strategy output. The methodologist then updated the strategy as necessary to capture all control articles. Databases were searched for studies published from January 2000 through May 2025. In addition to the MEDLINE and EMBASE databases searches, reference lists of included systematic reviews and primary literature were scanned for potentially useful studies.
GUIDELINE STATEMENTS
Pre-Operative Evaluation And Preparation
- For adult and pediatric patients undergoing surgical intervention for kidney and/or ureteral stones, clinicians should obtain a medical history, perform a relevant physical examination, and obtain laboratory studies appropriate to procedural risk and patient comorbidities. (Clinical Principle)
- For adult and pediatric patients with kidney and/or ureteral stones, clinicians should obtain a urinalysis and/or urine culture prior to surgical intervention. (Clinical Principle)
- For adult and pediatric patients with kidney and/or ureteral stones and untreated bacteriuria/funguria, clinicians should not proceed with definitive stone surgery. (Clinical Principle)
- For adult patients with kidney and/or ureteral stones, clinicians may obtain cross-sectional imaging to guide surgical treatment selection. (Conditional Recommendation; Evidence Level: Grade C)
- For adult patients undergoing percutaneous nephrolithotomy (PCNL) for kidney and/or ureteral stones, clinicians should obtain a computed tomography (CT) prior to surgery. (Moderate Recommendation; Evidence Level: Grade C)
- For adult and pediatric patients undergoing surgical intervention, clinicians should assess differential renal function if there is suspicion of clinically relevant loss of renal function in the involved kidney. (Expert Opinion)
Treatment Of Patients With Ureteral Stones
- For adult and pediatric patients with ≤10 mm distal ureteral stones, clinicians should offer medical expulsive therapy (MET) with alpha-adrenergic blockers for approximately 30 days to facilitate stone passage. (Strong Recommendation; Evidence Level: Grade A)
- For adult patients with ≤10 mm stones in the middle and proximal ureter, clinicians may offer MET with alpha-adrenergic blockers for approximately 30 days to facilitate stone passage. (Conditional Recommendation; Evidence Level: Grade B)
- When surgical treatment is indicated for adult patients with distal ureteral stones ≤10 mm, clinicians may offer ureteroscopy (URS) or shockwave lithotripsy (SWL). (Conditional Recommendation; Evidence Level: Grade B)
- When surgical treatment is indicated for adult patients with <2 cm proximal ureteral stones, clinicians may offer URS or SWL. (Conditional Recommendation; Evidence Level: Grade B)
- For adult patients with ureteral stones in whom SWL fails to result in complete stone clearance, clinicians may offer a second SWL procedure or proceed to URS. If a second SWL procedure fails, clinicians should offer URS. (Conditional Recommendation; Evidence Level: Grade C)
- For adult and pediatric patients with >2 cm ureteral stones or with ureteral stones that have not been successfully treated with previous retrograde URS or SWL or are not amenable to these procedures, clinicians should offer a percutaneous antegrade approach. (Expert Opinion)
Treatment Of Patients With Kidney Stones
- For adult patients with flank pain and non-obstructing kidney stones on the ipsilateral side who have no other identifiable source of pain, clinicians may offer elective surgical treatment. (Conditional Recommendation; Evidence Level: Grade C)
- For adult and pediatric patients with asymptomatic non-obstructing kidney stones, clinicians may offer either active surveillance or pre-emptive surgical intervention. (Conditional Recommendation; Evidence Level: Grade C)
- For adult patients with recurrent or persistent urinary tract infections (UTIs) and non-obstructing calyceal stones, clinicians may offer elective surgical stone removal for the purpose of reducing the risk of recurrent UTIs. (Conditional Recommendation; Evidence Level: Grade C)
- For adult patients undergoing SWL for kidney stones, clinicians may initiate treatment with low energy shockwaves and gradually increase the energy during the session in order to reduce the risk of bleeding complications. (Conditional Recommendation; Evidence Level: Grade C)
- For adult patients with <1 cm lower pole kidney stones, clinicians may offer SWL, URS, or a percutaneous approach after engaging in shared decision-making. (Expert Opinion)
- For adult patients with >1 cm lower pole or >2 cm non-lower pole kidney stones, clinicians should not offer SWL as first-line therapy. (Expert Opinion)
- For adult patients with >1 cm lower pole kidney stones, clinicians should inform the patient that PCNL is associated with a higher stone-free rate than SWL or URS. (Strong Recommendation; Evidence Level: Grade A)
- For adult patients with <2 cm lower pole stones undergoing URS with laser lithotripsy, clinicians should, when feasible, reposition the stone to a more superior location prior to lithotripsy. (Moderate Recommendation; Evidence Level: Grade B)
- For adult patients with 1 to 2 cm kidney stones, clinicians may offer mini-percutaneous nephrolithotomy (mini-PCNL), when available, over URS because of higher stone-free rates. (Conditional Recommendation; Evidence Level: Grade B)
- For adult patients with >2 cm kidney stones, clinicians should recommend PCNL as first-line therapy. (Moderate Recommendation; Evidence Level: Grade B)
- For adult patients undergoing PCNL for kidney stones up to 3 cm in size, clinicians may offer standard or mini-PCNL. (Conditional Recommendation; Evidence Level: Grade B)
Clinicians should inform these patients that mini-PCNL has stone-free rates comparable to standard PCNL but is associated with fewer complications, less pain, and shorter length of stay, but with a longer operative time. (Moderate Recommendation; Evidence Level: Grade C)
- Clinicians may perform PCNL in adult patients without discontinuing daily low dose aspirin. (Conditional Recommendation; Evidence Level: Grade C)
- For adult patients undergoing PCNL for kidney stones, clinicians may administer systemic tranexamic acid (TXA) at the time of PCNL to reduce blood loss, provided they have no contraindications. (Conditional Recommendation; Evidence Level: Grade A)
- For adult patients undergoing PCNL, clinicians may utilize either prone or supine positioning. (Conditional Recommendation; Evidence Level: Grade B)
- For adult patients undergoing PCNL for kidney stones, clinicians may utilize intraoperative ultrasound (US), fluoroscopy, or combination image guidance for access. (Conditional Recommendation; Evidence Level: Grade B)
- When performing mini-PCNL in adult patients with kidney or proximal ureteral stones, clinicians may utilize a suction sheath, when available, to improve stone-free rates and reduce the need for secondary procedures. (Conditional Recommendation; Evidence Level: Grade C)
- For adult patients with kidney stones undergoing PCNL, clinicians may omit nephrostomy tube placement, regardless of whether or not a ureteral stent is placed. (Conditional Recommendation; Evidence Level: Grade A)
- For adult patients undergoing PCNL, clinicians may obtain a CT in the immediate/early post-operative period to assess stone-free status and determine the need for a secondary procedure.(Expert Opinion)
Treatment Of Patients With Kidney And/Or Ureteral Stones
- In adult and pediatric patients with kidney and/or ureteral stones, clinicians should minimize ionizing radiation during surgical stone procedures using radiation-reducing techniques. (Expert Opinion)
- Clinicians should inform adult and pediatric patients with kidney and/or ureteral stones that URS is associated with a higher stone-free rate than SWL. (Strong Recommendation; Evidence Level: Grade B)
- In adult patients with kidney or ureteral stones in whom ureteroscopic, extracorporeal, or percutaneous treatment is unavailable, unsuccessful, or limited by patient factors, clinicians may perform a laparoscopic/robotic pyelolithotomy or ureterolithotomy. (Conditional Recommendation; Evidence Level: Grade C)
- For adult patients with kidney or ureteral stones undergoing SWL, clinicians may omit pre-operative prophylactic antibiotics. (Conditional Recommendation; Evidence Level: Grade B)
- For adult patients with kidney or ureteral stones undergoing URS and PCNL, clinicians should administer pre-operative prophylactic antibiotics. (Moderate Recommendation; Evidence Level: Grade B)
- For adult and pediatric patients with obstructing stones and suspected infection, clinicians should obtain a complete blood count, basic metabolic panel, urinalysis, and urine culture to assess for infection and guide clinical decision-making. (Expert Opinion)
- For adult patients with obstructing kidney and/or ureteral stones and suspected infection, clinicians should initiate urgent renal drainage. (Strong Recommendation; Evidence Level: Grade C)
For adult patients with obstructing kidney and/or ureteral stones and suspected infection, clinicians may drain the collecting system with either a nephrostomy tube or ureteral stent. (Conditional Recommendation; Evidence Level: Grade A)
For adult and pediatric patients with obstructing kidney and/or ureteral stones and suspected infection undergoing urgent drainage of the collecting system, clinicians should obtain a urine sample from the collecting system for culture, when possible. (Expert Opinion)
- For adult patients undergoing URS or PCNL for a primary, symptomatic ureteral or kidney stone, clinicians should offer concurrent URS removal of secondary, asymptomatic non-obstructing kidney stones <6 mm in either kidney during the same surgical session. (Moderate Recommendation; Evidence Level: Grade B)
- For adult patients with bilateral kidney and/or ureteral stones, clinicians may offer bilateral same-session stone treatment. (Conditional Recommendation; Evidence Level: Grade B)
- For adult and pediatric patients undergoing bilateral stone surgery or surgery in a functionally solitary kidney, clinicians should place a ureteral stent. (Expert Opinion)
- For adult patients with kidney and/or ureteral stones undergoing SWL, clinicians should not place a ureteral stent with the intention of improving stone-free rate. (Clinical Principle)
- For adult and pediatric patients undergoing SWL for kidney or ureteral stones, clinicians should employ a slow shockwave strategy to optimize stone clearance and minimize complications. (Moderate Recommendation; Evidence Level: Grade C)
- For adult patients undergoing SWL for kidney and/or ureteral stones, clinicians should prescribe post-operative alpha-adrenergic blockers to improve stone-free rates and reduce post-operative pain. (Strong Recommendation; Evidence Level: Grade B)
- Clinicians may perform URS for adult patients with kidney and/or ureteral stones who have uncorrected bleeding diatheses or who require continued anticoagulant (AC)/antiplatelet (AP) therapy. (Conditional Recommendation; Evidence Level: Grade C)
- For adult patients with kidney and/or ureteral stones, clinicians may offer primary URS without prior stent placement. (Expert Opinion)
- For adult patients with kidney and/or ureteral stones undergoing URS, clinicians may use a ureteral access sheath (UAS). (Conditional Recommendation; Evidence Level: Grade B)
- For adult patients with kidney and/or ureteral stones undergoing URS with a UAS, clinicians may choose a flexible and navigable suction UAS. (Conditional Recommendation: Evidence Level: Grade C)
- Clinicians may use a single-use flexible ureteroscope or reusable flexible ureteroscope for adult patients undergoing URS for kidney and/or ureteral stones. (Conditional Recommendation; Evidence Level: Grade A)
- For adult patients undergoing URS with laser lithotripsy for kidney and/or ureteral stones, clinicians may utilize either a holmium:YAG or thulium fiber laser. (Conditional Recommendation; Evidence Level: Grade C)
- For adult and pediatric patients undergoing URS with laser lithotripsy for kidney and/or ureteral stones, clinicians should utilize laser settings with the lowest total power that will accomplish clinical stone ablation. (Expert Opinion)
- For adult and pediatric patients undergoing URS with laser lithotripsy for kidney and/or ureteral stones, clinicians may utilize a strategy of fragmenting and basketing or “dusting”. (Conditional Recommendation; Evidence Level: Grade B)
- For adult patients with kidney and/or ureteral stones, clinicians may omit post-operative ureteral stent placement following uncomplicated URS. (Conditional Recommendation; Evidence Level: Grade C)
- For adult and pediatric patients undergoing surgical intervention for kidney and/or ureteral stones, clinicians should obtain stone for analysis when possible. (Clinical Principle)
- For adult patients undergoing surgical intervention for kidney and/or ureteral stones, clinicians should utilize a multi-modal, non-opioid analgesic regimen and minimize use of opioids for post-operative pain management. (Moderate Recommendation; Evidence Level: Grade C)
- For adult and pediatric patients undergoing surgical intervention for kidney and/or ureteral stones, clinicians should order follow-up imaging to assess residual stone burden and to identify hydronephrosis or other procedure-related complications. (Expert Opinion)
- For adult and pediatric patients with residual stones after undergoing surgical intervention for kidney and/or ureteral stones, clinicians should offer secondary endoscopic removal of residual fragments and engage in shared decision-making, taking into account the benefits and risks. (Moderate Recommendation; Evidence Level: Grade C)
Treatment Of Pregnant Patients With Kidney And/Or Ureteral Stones
- For pregnant patients with suspected symptomatic kidney and/or ureteral stones, clinicians should utilize US as first-line imaging. If further imaging is indicated, non-contrast magnetic resonance imaging (MRI) or CT are both appropriate alternatives. (Expert Opinion)
- For pregnant patients with symptomatic kidney and/or ureteral stones, clinicians should coordinate pharmacologic and/or surgical intervention with the obstetrician. (Clinical Principle)
- For pregnant patients with kidney and/or ureteral stones and well controlled symptoms, clinicians should offer observation with a trial of stone passage. (Clinical Principle)
- For pregnant patients with ureteral stones for whom a trial of passage is unsuccessful or who are not candidates for a trial of passage, clinicians may offer URS. Placement of a ureteral stent or nephrostomy tube, with frequent tube changes, may be offered as an alternative to URS. (Conditional Recommendation; Evidence Level: Grade C)
INTRODUCTION
Background
Approximately 1 in 9 individuals in the United States will be diagnosed with a kidney or ureteral stone at some time in their lives, and there is evidence that this number is rising in some populations, including women.1-3 Although some stones remain asymptomatic and are evident only as an incidental finding on imaging studies obtained for unrelated reasons, others are manifested through episodes of pain, infection or loss of kidney function. Acute symptoms from kidney or ureteral stones are responsible for over one million emergency department (ED) visits annually in the US,4 with a 17.9% increase in ED visits documented between 2006 and 2014.5 Many of these visits culminate in hospital admission and/or surgical intervention, underscoring the heavy economic burden on the healthcare system attributable to stone disease. Indeed, over 370,000 commercially insured individuals and Medicare beneficiaries underwent surgery for stones in 2019, with the majority of procedures comprised of URS.1 However, absolute increases in the number of patients undergoing both URS and PCNL have been observed, while absolute numbers of SWL procedures and the proportion of stone procedures performed as SWL declined from 2011 to 2019.1
Safe, efficient, and cost-effective management of symptomatic and/or high risk renal and ureteral stones (i.e., large, obstructing, renal pelvis or ureteral, or infection-related stones or stones in anatomically or functionally solitary kidneys) requires careful planning based on patient history and relevant diagnostic imaging. Patient factors, anatomic considerations and stone characteristics will determine the optimal timing and selection of surgical treatment modalities. Furthermore, appropriate and timely follow-up determines the success and identifies complications of surgical intervention. The American Urological Association (AUA) has been committed to providing evidence-based recommendations for the comprehensive surgical management of patients with kidney and/or ureteral stones, including the decision to observe, rather than to treat select patients, since publication of the initial Guidelines on Management of Staghorn Calculi in 2005 and Ureteral Calculi in 2007.6, 7 The prior Surgical Management of Stones Guideline, which incorporated recommendations for the treatment of patients with kidney and/or ureteral stones, was released in 2016 and was based on peer-reviewed literature from 1/1/1985 to 5/31/2015.8 In the current Guideline, the literature search included articles published between January 2000 through May 2025. The overlap of articles published between 2000 and 2015 between the two Guidelines was primarily because most SWL literature was published before 2015, and some other relevant key trials that have not been replicated fell within that time frame. The Panel’s intention was not to simply expand upon the previous systematic review from the 2016 Guideline, but rather to limit the search to a time frame that reflects modern endoscopic and non-invasive surgical modalities. While this limited search may miss some important historical findings from older relevant published studies, the intention of the Panel was to utilize the best contemporary evidence available on which to base the recommendations. In addition, consistent with the prior Guideline, the Panel included SWL among “surgical” stone treatments, despite its non-invasive nature, based on general convention.
In order to provide evidence-based recommendations that encompass the most common clinical patient scenarios, the Panel specified the patient population for which each statement is intended. However, unless otherwise specified, the population addressed in the Guideline statements should be assumed to be non-pregnant with an anatomically normal urinary tract. The lack of extensive published data on the surgical management of stones in pediatric patients precluded a clear set of Guideline recommendations in this patient population. Consequently, where sufficient data exist to support evidence-based directives for pediatric patients, separate Guideline statements were developed. However, when sufficient evidence was unavailable, but the Panel surmised that the recommendations for adult patients could be reasonably applied to the pediatric population based on Expert Opinion, their recommendations were added to the supporting documentation for the corresponding Guideline statements based on evidence in the adult population.
For the purposes of this Guideline, ureteral stone locations are categorized as proximal –extending from the ureteropelvic junction to the superior border of the sacroiliac joint; middle – overlying the bony pelvis; and distal – from the inferior border of the sacroiliac joint to the ureterovesical junction.
METHODOLOGY
Determination of the Guideline scope and assessment of the final systematic review to inform Guideline statements was conducted in conjunction with the Stones Guideline Panel. The systematic review utilized to inform this Guideline and methodological support was provided by an independent methodological consultant.
Panel Formation
The Panel was created in 2023 by the American Urological Association Education and Research, Inc. (AUAER). The Practice Guidelines Committee (PGC) of the AUA selected the Panel Chairs who in turn appointed the additional panel members following an open nomination process to identify members with specific expertise in this area. This is a multidisciplinary panel that includes representation from urology/endourology, endocrinology, and urology nutrition, in addition to patient representation. Funding for the Panel was provided by the AUA; panel members received no remuneration for their work.
Searches and Article Selection
As stated above, the systematic review that informs the Guideline statements was conducted in two planned stages, including a search for systematic reviews followed by a search for primary literature. An initial search was conducted for existing systematic reviews in March 2024 and an updated search was conducted to capture studies through May 2025. Systematic reviews published as a component of practice guidelines were also considered eligible for inclusion. An electronic search employing OVID was used to systematically search the MEDLINE and EMBASE databases, as well as the Cochrane Library, for systematic reviews evaluating surgical management of kidney and ureteral stones.
OVID was used to systematically search MEDLINE and EMBASE databases for articles evaluating surgical management of kidney and ureteral stones using the population, interventions, comparisons, and outcomes (PICO) as outlined below. During PICO development, panel members submitted landmark studies addressing the Key Questions to the methodologist. These studies were defined as control articles and were used to harvest terms for the search strategy. Additionally, the literature search strategy output was compared to the control articles to test for precision and recall in the search, with the strategy being updated as necessary to capture all control articles. Databases were searched for studies published from January 2000 through May 2025. In addition to the MEDLINE and EMBASE databases searches, reference lists of included systematic reviews and primary literature were scanned for potentially useful studies.
All articles identified from the OVID literature search were entered into reference management software (EndNote 21), where duplicate citations were removed. Abstracts were reviewed by the methodologist to determine if the study addressed the Key Questions and if the Patient, Intervention, Comparison, and Outcome (PICO) criteria were met. For all research questions, randomized controlled trials (RCTs), observational studies, and case-control studies were considered for inclusion in the evidence base. Single arm studies were only considered for Key Questions where a paucity of comparative studies was expected. All studies had to enroll at least 30 patients per study arm. Case series, letters, editorials, in vitro studies, studies conducted in animal models, and studies not published in English were excluded from the evidence base a priori.
Full-text review was conducted on studies that passed the abstract screening phase. Fifteen panel members were paired with the methodologist and completed duplicate full-text study selections of 50 random studies undergoing full-text review. The dual-review trained the methodologist, who then completed full-time review of the remaining studies.
Following the full-text review, 25 systematic reviews met the study selection criteria and were included in the evidence base.
The primary literature review was used to address all outcomes not covered by the included systematic reviews. It was anticipated that primary literature would report on outcomes in addition to what was pooled in the 25 included systematic reviews. As such, the literature search for primary literature was not altered following selection of the systematic review into the evidence base. Instead, where overlap was recognized between studies included in the identified systematic reviews and identified primary studies, primary studies were either removed from the evidence base, or when primary literature reported on additional outcomes, overlapping outcomes were not extracted in the primary literature. This methodology ensured that data were not included twice in the evidence base, as this could result in an overestimate of effect. A total of 809 primary literature studies were identified that met the inclusion criteria. An updated search was conducted from March 2024 through May 2025 which captured an additional 114 new studies.
The primary literature review was used to address all outcomes not covered by the included systematic reviews. It was anticipated that primary literature would report on outcomes in addition to what was pooled in the 25 included systematic reviews. As such, the literature search for primary literature was not altered following selection of the systematic review into the evidence base. Instead, where overlap was recognized between studies included in the identified systematic reviews and identified primary studies, primary studies were either removed from the evidence base, or when primary literature reported on additional outcomes, overlapping outcomes were not extracted in the primary literature. This methodology ensured that data were not included twice in the evidence base, as this could result in an overestimate of effect. A total of 809 primary literature studies were identified that met the inclusion criteria. An updated search was conducted from March 2024 through May 2025 which captured an additional 114 new studies.
Data Abstraction
Data were extracted from all studies that passed full-text review by an independent methodologist.
Risk of Bias Assessment
Individual Study Quality and Potential for Bias
Quality assessment for all retained studies was conducted. Using this method, studies deemed to be of low quality would not be excluded from the systematic review, but would be retained, and their methodological strengths and weaknesses discussed where relevant. To define an overall study quality rating for each included study, risk of bias as determined by validated study-type specific tools, was paired with additional important quality features. To evaluate the risk of bias within the identified studies, the Assessment of Multiple Systematic Reviews 2 (AMSTAR 2)9 tool was used for systematic reviews, the Cochrane Risk of Bias Tool 210 was used for randomized studies, and a Risk of Bias in Non-Randomized Studies – of Intervention (ROBINS-I)11 was used for observational studies. Additional important quality features, such as study design, comparison type, power of statistical analysis, and sources of funding were extracted for each study.
Data Synthesis
Review Manager version 5.412 was used to perform meta-analysis and generate forest plots when data were homogeneous and poolable using a random-effects model. For dichotomous outcomes (stone-free rate, stone clearance rate, complication rate, rate of surgical intervention, rate of emergency department visits), risk ratios were calculated using the Mantel-Haenszel method (M-H), while for continuous outcomes (pain episodes, pain medication dosage), mean differences (MD) were calculated using an inverse variance method. Statistical heterogeneity was assessed using the Higgins I2 value and the chi square test. A Higgins’ I2 value >50% and p-values <0.05 were considered to represent significant heterogeneity. Causes of heterogeneity were explored by subgroup analysis. Subgroup analyses were also conducted for stone size and stone locations when appropriate.
Determination of Evidence Strength
The Grading of Recommendations Assessment, Development, and Evaluation (GRADE)13 system was used to determine the aggregate evidence quality for each outcome, or group of related outcomes, informing Key Questions. GRADE defines a body of evidence in relation to how confident guideline developers can be that the estimate of effects as reported by that body of evidence, is correct. Evidence is categorized as high, moderate, low, and very low, and assessment is based on the aggregate risk of bias for the evidence base, plus limitations introduced as a consequence of inconsistency, indirectness, imprecision, and publication bias across the studies.14 Additionally, certainty of evidence can be downgraded if confounding across the studies has resulted in the potential for the evidence base to overestimate the effect. Upgrading of evidence is possible if the body of evidence indicates a large effect or if confounding would suggest either spurious effects or would reduce the demonstrated effect.
The AUA employs a 3-tiered strength of evidence system to underpin evidence-based guideline statements. Table 1 summarizes the GRADE categories, definitions, and how these categories translate to the AUA strength of evidence categories. In short, high certainty by GRADE translates to AUA A-category strength of evidence, moderate to B, and both low and very low to C.
The AUA categorizes body of evidence strength as Grade A, Grade B, or Grade C. By definition, Grade A evidence is evidence about which the Panel has a high level of certainty, Grade B evidence is evidence about which the Panel has a moderate level of certainty, and Grade C evidence is evidence about which the Panel has a low level of certainty.15
AUA Nomenclature: Linking Statement Type to Evidence Strength
The AUA nomenclature system explicitly links statement type to body of evidence strength, level of certainty, magnitude of benefit or risk/burdens, and the Panel’s judgment regarding the balance between benefits and risks/burdens (Table 2). Strong Recommendations are directive statements that an action should (benefits outweigh risks/burdens) or should not (risks/burdens outweigh benefits) be undertaken because net benefit or net harm is substantial. Moderate Recommendations are directive statements that an action should (benefits outweigh risks/burdens) or should not (risks/burdens outweigh benefits) be undertaken because net benefit or net harm is moderate. Conditional Recommendations are non-directive statements used when the evidence indicates that there is no apparent net benefit or harm, or when the balance between benefits and risks/burden is unclear. All three statement types may be supported by any body of evidence strength grade. Body of evidence strength Grade A in support of a Strong or Moderate Recommendation indicates that the statement can be applied to most patients in most circumstances and future research is unlikely to change confidence. Body of evidence strength Grade B in support of a Strong or Moderate Recommendation indicates that the statement can be applied to most patients in most circumstances, but better evidence could change confidence. Body of evidence strength Grade C in support of a Strong or Moderate Recommendation indicates that the statement can be applied to most patients in most circumstances, but better evidence is likely to change confidence. Conditional Recommendations also can be supported by any evidence strength. When body of evidence strength is Grade A, the statement indicates that benefits and risks/burdens appear balanced, the best action depends on patient circumstances, and future research is unlikely to change confidence. When body of evidence strength Grade B is used, benefits and risks/burdens appear balanced, the best action also depends on individual patient circumstances and better evidence could change confidence. When body of evidence strength Grade C is used, there is uncertainty regarding the balance between benefits and risks/burdens, alternative strategies may be equally reasonable, and better evidence is likely to change confidence.
Where gaps in the evidence existed, the Panel provides guidance in the form of Clinical Principles or Expert Opinions with consensus achieved using a modified Delphi technique if differences in opinion emerged.16 A Clinical Principle is a statement about a component of clinical care that is widely agreed upon by urologists or other clinicians for which there may or may not be evidence in the medical literature. Expert Opinion refers to a statement, achieved by consensus of the Panel, that is based on members’ clinical training, experience, knowledge, and judgment.
Peer Review and Document Approval
An integral part of the guideline development process at the AUA is external peer review. The AUA conducted a thorough peer review process to ensure that the document was reviewed by experts who were knowledgeable in the area of urinary stone disease. In addition to reviewers from the AUA PGC, Science and Quality Council (SQC), and Board of Directors (BOD), the document was reviewed by external content experts. Additionally, a call for reviewers was placed on the AUA website from April 23, 2025 to May 7, 2025 to allow any additional interested parties to request a copy of the document for review. Additional notifications were sent through various AUA membership and patient advocacy channels to further promote the availability of the document for review. The draft Guideline was distributed to 225 peer reviewers. All peer review comments were blinded and sent to the Panel for review. In total, 148 reviewers provided comments. At the end of the peer review process, a total of 1,596 comments were received. Following comment discussion, the Panel revised the draft as needed. Once finalized, the Guideline was submitted to the AUA PGC, SQC, and BOD for final approval.
GUIDELINE STATEMENTS
Pre-Operative Evaluation and Preparation
Guideline Statement 1
For adult and pediatric patients undergoing surgical intervention for kidney and/or ureteral stones, clinicians should obtain a medical history, perform a relevant physical examination, and obtain laboratory studies appropriate to procedural risk and patient comorbidities. (Clinical Principle)
Guideline Statement 2
For adult and pediatric patients with kidney and/or ureteral stones, clinicians should obtain a urinalysis and/or urine culture prior to surgical intervention. (Clinical Principle)
Guideline Statement 3
For adult and pediatric patients with kidney and/or ureteral stones and untreated bacteriuria/funguria, clinicians should not proceed with definitive stone surgery. (Clinical Principle)
Guideline Statement 4
For adult patients with kidney and/or ureteral stones, clinicians may obtain cross-sectional imaging to guide surgical treatment selection. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 5
For adult patients undergoing PCNL for kidney and/or ureteral stones, clinicians should obtain a CT prior to surgery. (Moderate Recommendation; Evidence Level: Grade C)
Guideline Statement 6
For adult and pediatric patients undergoing surgical intervention, clinicians should assess differential renal function if there is suspicion of clinically relevant loss of renal function in the involved kidney. (Expert Opinion)
Treatment of Patients With Ureteral Stones
Guideline Statement 7
For adult and pediatric patients with ≤10 mm distal ureteral stones, clinicians should offer MET with alpha-adrenergic blockers for approximately 30 days to facilitate stone passage. (Strong Recommendation; Evidence Level: Grade A)
Guideline Statement 8
For adult patients with ≤10 mm stones in the middle and proximal ureter, clinicians may offer MET with alpha-adrenergic blockers for approximately 30 days to facilitate stone passage. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 9
When surgical treatment is indicated for adult patients with distal ureteral stones ≤10 mm, clinicians may offer URS or SWL. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 10
When surgical treatment is indicated for adult patients with <2 cm proximal ureteral stones, clinicians may offer URS or SWL. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 11
For adult patients with ureteral stones in whom SWL fails to result in complete stone clearance, clinicians may offer a second SWL procedure or proceed to URS. If a second SWL procedure fails, clinicians should offer URS. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 12
For adult and pediatric patients with >2 cm ureteral stones or with ureteral stones that have not been successfully treated with previous retrograde URS or SWL or are not amenable to these procedures, clinicians should offer a percutaneous antegrade approach. (Expert Opinion)
Treatment of Patients With Kidney Stones
Guideline Statement 13
For adult patients with flank pain and non-obstructing kidney stones on the ipsilateral side who have no other identifiable source of pain, clinicians may offer elective surgical treatment. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 14
For adult and pediatric patients with asymptomatic non-obstructing kidney stones, clinicians may offer either active surveillance or pre-emptive surgical intervention. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 15
For adult patients with recurrent or persistent UTIs and non-obstructing calyceal stones, clinicians may offer elective surgical stone removal for the purpose of reducing the risk of recurrent UTIs. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 16
For adult patients undergoing SWL for kidney stones, clinicians may initiate treatment with low energy shockwaves and gradually increase the energy during the session in order to reduce the risk of bleeding complications. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 17
For adult patients with <1 cm lower pole kidney stones, clinicians may offer SWL, URS, or a percutaneous approach after engaging in shared decision-making. (Expert Opinion)
Guideline Statement 18
For adult patients with >1 cm lower pole or >2 cm non-lower pole kidney stones, clinicians should not offer SWL as first-line therapy. (Expert Opinion)
Guideline Statement 19
For adult patients with >1 cm lower pole kidney stones, clinicians should inform the patient that PCNL is associated with a higher stone-free rate than SWL or URS. (Strong Recommendation; Evidence Level: Grade A)
Guideline Statement 20
For adult patients with <2 cm lower pole stones undergoing URS with laser lithotripsy, clinicians should, when feasible, reposition the stone to a more superior location prior to lithotripsy. (Moderate Recommendation; Evidence Level: Grade B)
Guideline Statement 21
For adult patients with 1 to 2 cm kidney stones, clinicians may offer mini-PCNL, when available, over URS because of higher stone-free rates. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 22
For adult patients with >2 cm kidney stones, clinicians should recommend PCNL as first-line therapy. (Moderate Recommendation; Evidence Level: Grade B)
Guideline Statement 23
For adult patients undergoing PCNL for kidney stones up to 3 cm in size, clinicians may offer standard or mini-PCNL. (Conditional Recommendation; Evidence Level: Grade B)
Clinicians should inform these patients that mini-PCNL has stone-free rates comparable to standard PCNL but is associated with fewer complications, less pain, and shorter length of stay, but with a longer operative time. (Moderate Recommendation; Evidence Level: Grade C)
Guideline Statement 24
Clinicians may perform PCNL in adult patients without discontinuing daily low dose aspirin. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 25
For adult patients undergoing PCNL for kidney stones, clinicians may administer systemic TXA at the time of PCNL to reduce blood loss, provided they have no contraindications. (Conditional Recommendation; Evidence Level: Grade A)
Guideline Statement 26
For adult patients undergoing PCNL, clinicians may utilize either prone or supine positioning. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 27
For adult patients undergoing PCNL for kidney stones, clinicians may utilize intraoperative US, fluoroscopy, or combination image guidance for access. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 28
When performing mini-PCNL in adult patients with kidney or proximal ureteral stones, clinicians may utilize a suction sheath, when available, to improve stone-free rates and reduce the need for secondary procedures. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 29
For adult patients with kidney stones undergoing PCNL, clinicians may omit nephrostomy tube placement, regardless of whether or not a ureteral stent is placed. (Conditional Recommendation; Evidence Level: Grade A)
Guideline Statement 30
For adult patients undergoing PCNL, clinicians may obtain a CT in the immediate/early post-operative period to assess stone-free status and determine the need for a secondary procedure.(Expert Opinion)
Treatment of Patients with Kidney and/or Ureteral Stones
Guideline Statement 31
In adult and pediatric patients with kidney and/or ureteral stones, clinicians should minimize ionizing radiation during surgical stone procedures using radiation-reducing techniques. (Expert Opinion)
Guideline Statement 32
Clinicians should inform adult and pediatric patients with kidney and/or ureteral stones that URS is associated with a higher stone-free rate than SWL. (Strong Recommendation; Evidence Level: Grade B)
Guideline Statement 33
In adult patients with kidney or ureteral stones in whom ureteroscopic, extracorporeal, or percutaneous treatment is unavailable, unsuccessful, or limited by patient factors, clinicians may perform a laparoscopic/robotic pyelolithotomy or ureterolithotomy. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 34
For adult patients with kidney or ureteral stones undergoing SWL, clinicians may omit pre-operative prophylactic antibiotics. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 35
For adult patients with kidney or ureteral stones undergoing URS and PCNL, clinicians should administer pre-operative prophylactic antibiotics. (Moderate Recommendation; Evidence Level: Grade B)
Guideline Statement 36
For adult and pediatric patients with obstructing stones and suspected infection, clinicians should obtain a complete blood count, basic metabolic panel, urinalysis, and urine culture to assess for infection and guide clinical decision-making. (Expert Opinion)
Guideline Statement 37
For adult patients with obstructing kidney and/or ureteral stones and suspected infection, clinicians should initiate urgent renal drainage. (Strong Recommendation; Evidence Level: Grade C)
For adult patients with obstructing kidney and/or ureteral stones and suspected infection, clinicians may drain the collecting system with either a nephrostomy tube or ureteral stent. (Conditional Recommendation; Evidence Level: Grade A)
For adult and pediatric patients with obstructing kidney and/or ureteral stones and suspected infection undergoing urgent drainage of the collecting system, clinicians should obtain a urine sample from the collecting system for culture, when possible. (Expert Opinion)
Guideline Statement 38
For adult patients undergoing URS or PCNL for a primary, symptomatic ureteral or kidney stone, clinicians should offer concurrent URS removal of secondary, asymptomatic non-obstructing kidney stones <6 mm in either kidney during the same surgical session. (Moderate Recommendation; Evidence Level: Grade B)
Guideline Statement 39
For adult patients with bilateral kidney and/or ureteral stones, clinicians may offer bilateral same-session stone treatment. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 40
For adult and pediatric patients undergoing bilateral stone surgery or surgery in a functionally solitary kidney, clinicians should place a ureteral stent. (Expert Opinion)
Guideline Statement 41
For adult patients with kidney and/or ureteral stones undergoing SWL, clinicians should not place a ureteral stent with the intention of improving stone-free rate. (Clinical Principle)
Guideline Statement 42
For adult and pediatric patients undergoing SWL for kidney or ureteral stones, clinicians should employ a slow shockwave strategy to optimize stone clearance and minimize complications. (Moderate Recommendation; Evidence Level: Grade C)
Guideline Statement 43
For adult patients undergoing SWL for kidney and/or ureteral stones, clinicians should prescribe post-operative alpha-adrenergic blockers to improve stone-free rates and reduce post-operative pain. (Strong Recommendation; Evidence Level: Grade B)
Guideline Statement 44
Clinicians may perform URS for adult patients with kidney and/or ureteral stones who have uncorrected bleeding diatheses or who require continued AC/AP therapy. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 45
For adult patients with kidney and/or ureteral stones, clinicians may offer primary URS without prior stent placement. (Expert Opinion)
Guideline Statement 46
For adult patients with kidney and/or ureteral stones undergoing URS, clinicians may use a UAS. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 47
For adult patients with kidney and/or ureteral stones undergoing URS with a UAS, clinicians may choose a flexible and navigable suction UAS. (Conditional Recommendation: Evidence Level: Grade C)
Guideline Statement 48
Clinicians may use a single-use flexible ureteroscope or reusable flexible ureteroscope for adult patients undergoing URS for kidney and/or ureteral stones. (Conditional Recommendation; Evidence Level: Grade A)
Guideline Statement 49
For adult patients undergoing URS with laser lithotripsy for kidney and/or ureteral stones, clinicians may utilize either a holmium:YAG or thulium fiber laser. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 50
For adult and pediatric patients undergoing URS with laser lithotripsy for kidney and/or ureteral stones, clinicians should utilize laser settings with the lowest total power that will accomplish clinical stone ablation. (Expert Opinion)
Guideline Statement 51
For adult and pediatric patients undergoing URS with laser lithotripsy for kidney and/or ureteral stones, clinicians may utilize a strategy of fragmenting and basketing or “dusting”. (Conditional Recommendation; Evidence Level: Grade B)
Guideline Statement 52
For adult patients with kidney and/or ureteral stones, clinicians may omit post-operative ureteral stent placement following uncomplicated URS. (Conditional Recommendation; Evidence Level: Grade C)
Guideline Statement 53
For adult and pediatric patients undergoing surgical intervention for kidney and/or ureteral stones, clinicians should obtain stone for analysis when possible. (Clinical Principle)
Guideline Statement 54
For adult patients undergoing surgical intervention for kidney and/or ureteral stones, clinicians should utilize a multi-modal, non-opioid analgesic regimen and minimize use of opioids for post-operative pain management. (Moderate Recommendation; Evidence Level: Grade C)
Guideline Statement 55
For adult and pediatric patients undergoing surgical intervention for kidney and/or ureteral stones, clinicians should order follow-up imaging to assess residual stone burden and to identify hydronephrosis or other procedure-related complications. (Expert Opinion)
Guideline Statement 56
For adult and pediatric patients with residual stones after undergoing surgical intervention for kidney and/or ureteral stones, clinicians should offer secondary endoscopic removal of residual fragments and engage in shared decision-making, taking into account the benefits and risks. (Moderate Recommendation; Evidence Level: Grade C)
Treatment for Pregnant Patients with Kidney and/or Ureteral Stones
Guideline Statement 57
For pregnant patients with suspected symptomatic kidney and/or ureteral stones, clinicians should utilize US as first-line imaging. If further imaging is indicated, non-contrast MRI or CT are both appropriate alternatives. (Expert Opinion)
Guideline Statement 58
For pregnant patients with symptomatic kidney and/or ureteral stones, clinicians should coordinate pharmacologic and/or surgical intervention with the obstetrician. (Clinical Principle)
Guideline Statement 59
For pregnant patients with kidney and/or ureteral stones and well controlled symptoms, clinicians should offer observation with a trial of stone passage. (Clinical Principle)
Guideline Statement 60
For pregnant patients with ureteral stones for whom a trial of passage is unsuccessful or who are not candidates for a trial of passage, clinicians may offer URS. Placement of a ureteral stent or nephrostomy tube, with frequent tube changes, may be offered as an alternative to URS. (Conditional Recommendation; Evidence Level: Grade C)
FUTURE DIRECTIONS
The intensive work that went into developing this Guideline has identified much that has been accomplished in advancing our understanding of the treatment of patients with kidney and ureteral stones but has also identified gaps in knowledge. Given the prevalence of this condition, efforts to fill these gaps will result in a broader understanding of how to treat patients optimally and will meaningfully benefit urologic practice. When we look towards what should be accomplished in the coming years, so that the next iteration of this Guideline will provide even more robust guidance for the practicing urologist, there are needs both in developing and refining novel treatment approaches and how the effectiveness of these treatments will be measured.
In the Future Directions discussion of the prior Surgical Management of Stones Guideline, there was a call for an improvement in devices and technologies that can more efficiently and safely fragment and evacuate stone material.8 In this Guideline, we now see the introduction of mini-PCNL and suction technologies. However, in many cases these technologies are still sensitive to the patient’s baseline stone burden. In other cases, such as utilizing high frequency lasers for a “dusting” approach to stone treatment, the outcomes appear to be inferior to the prior technique of basket extraction. As always, future efforts should continue to be devoted to improving the efficiency of stone removal through less invasive platforms as this will continue to further benefit patients. During the drafting of this Guideline, it has been apparent that novel therapies have recently arrived or are going to be arriving in the clinical domain. Among these therapies are suction-based retrograde approaches, ultrasonic propulsion burst wave lithotripsy, robotic platforms, hybrid lasers, and the ability to monitor collecting system temperature and pressure. Importantly, as these novel technologies and techniques are introduced, they should be rigorously and critically assessed in clinical investigations that employ clearly described, high quality imaging, and adhere to standardized definitions of treatment outcomes.
As has been noted in many of the AUA Guideline documents, not just those focused on kidney and ureteral stone disease, there is a paucity of high-quality RCTs in the urologic field that compare outcomes for surgical interventions. In addition to this Guideline serving as a call for future studies of high-quality design, there is also a need to ensure that the reporting of outcomes in these studies is standardized and reproducible. In many cases, this Guideline was challenged by heterogenous reporting of not just basic factors such as stone location in the ureter, but also treatment approaches such as laser settings or lithotripter choice as well as treatment outcomes. This, unfortunately, limited the meta-analytic approach the Panel could take regarding comparative effectiveness of competing therapies. There is also a recognition that stone treatment outcomes are more nuanced than the binary outcome of stone-free/not stone-free and should include measures such as stone clearance (percent volume reduction) and residual stone burden (stone volume remaining) that can be calculated via CT imaging.
And lastly, but perhaps most importantly, understanding the patient perspective on the treatment of stones is limited, and there has been little investigation into the methodology of shared decision-making. There is a need for study designs that include patient-reported outcomes such as quality of life effects. In addition, fundamental questions that patients will ask a urologist, such as how long it will take for a ureteral stone to pass, when to intervene on an asymptomatic stone, how to optimally treat stent discomfort, and whether anything can be done to promote stone passage, remain largely unanswered. Including the patient perspective in this Guideline served to underscore these important considerations and should be front-of-mind as we design future studies assessing the quality and outcomes of stone treatment.
TOOLS AND REFERENCES
ABBREVIATIONS
| 95% CI | 95% confidence interval |
| AC | Anticoagulant |
| ACOG | American College of Obstetrics and Gynecology |
| ALARA | As Low As Reasonably Achievable |
| AMSTAR 2 | Assessment of Multiple Systematic Reviews 2 |
| aOR | Adjusted odds ratio |
| AP | Antiplatelet |
| AUA | American Urological Association |
| AUAER | American Urological Association Education and Research, Inc. |
| BMI | Body mass index |
| BOD | Board of Directors |
| CROES | The Clinical Research Office of the Endourological Society |
| CRP | C-reactive protein |
| CT | Computed tomography |
| CUA | Canadian Urological Association |
| DMSA | Dimercaptosuccinic acid |
| E. coli | Escherichia coli |
| ED | Emergency department |
| EAU | The European Association of Urology |
| ECIRS | Endoscopic combined intrarenal surgery |
| FANS-UAS | Flexible and navigable suction ureteral access sheath |
| GRADE | Grading of Recommendations Assessment, Development, and Evaluation |
| HR | Hazard ratio |
| IV | Intravenous |
| KUB | Kidney, ureter, bladder radiography |
| MAG-3 | Mercaptoacetyltriglycine |
| MET | Medical expulsive therapy |
| MD | Mean difference |
| M-H | Mantel-Haenszel method |
| Mini-PCNL | Mini-percutaneous nephrolithotomy |
| MRI | Magnetic resonance imaging |
| MUSIC | The Michigan Urological Surgery Improvement Collaborative |
| NCCT | Non-contrast computed tomography |
| NSAID | Nonsteroidal anti-inflammatory drug |
| OR | Odds ratio |
| PCN | Percutaneous nephrostomy |
| PCNL | Percutaneous nephrolithotomy |
| PGC | Practice Guidelines Committee |
| PICO | Patient, Intervention, Comparison, and Outcome |
| PPV | Positive predictive value |
| QALY | Quality-Adjusted Life Years |
| Random | Random effect model |
| RCS | Retrospective cohort study |
| RCT | Randomized controlled trial |
| RI | Resistive index |
| RIRS | Retrograde intrarenal surgery |
| ROBINS-I | Risk of Bias in Non-Randomized Studies |
| RR | Risk ratio |
| SIRS | Systemic inflammatory response syndrome |
| spm | Shocks per minute |
| SQC | Science & Quality Council |
| SUFU | Society of Urodynamics, Female Pelvic Medicine & Urogenital Reconstruction |
| SWL | Shockwave lithotripsy |
| TXA | Tranexamic acid |
| UAS | Ureteral access sheath |
| URS | Ureteroscopy |
| US | Ultrasound |
| UTI | Urinary tract infection |
| WMD | Weighted mean difference |
APPENDIX
APPENDIX 1. META-ANALYSIS MEDICAL EXPULSIVE THERAPY VERSUS STANDARD OF CARE
Appendix 1 References
References for Appendix 1a.
Stone Clearance for Medical Expulsive Therapy versus Standard of Care by Stone Location |
Distal |
Abdel-Meguid et al. 2010351 |
Afridi et al. 2024352 |
Agrawal et al. 2009353 |
Ahmad et al. 2015354 |
Ahmed and Al-Sayed 2010355 |
Al-Ansari et al. 2010356 |
Albert et al. 2016357 |
Aldemir et al. 2011358 |
Autorino et al. 2005359 |
Bajwa et al. 2013360 |
Bashir et al. 2023361 |
Bayraktar and Albayrak 2017362 |
Cervenàkov et al. 2002363 |
Cha et al. 2012364 |
Doluoglu et al. 2015365 |
Erkan et al. 2011366 |
Erturhan et al. 2007367 |
Falahatkar et al. 2021368 |
Furyk et al. 2016369 |
Griwan et al. 2010370 |
Han et al. 2006371 |
Hermanns et al. 2009372 |
Ibrahim et al. 2013373 |
Islam et al. 2012374 |
Itoh et al. 2011375 |
Itoh et al. 2013376 |
Kim et al. 2007377 |
Liatsikos et al. 2007378 |
Lojanapiwat et al. 2008379 |
Maitra 2012380 |
Mshemish 2012381 |
Mukhtarov et al. 2007382 |
Nuraj and Hyseni 2017383 |
Ochoa-Gómez et al. 2011384 |
Pickard et al. 2015385 |
Porpiglia et al. 2009386 |
Rahim et al. 2012387 |
Samir et al. 2023388 |
Sayed et al. 2008389 |
Sen et al. 2017390 |
Sur et al. 2015391 |
Taghavi et al. 2005392 |
Vincendeau et al. 2010393 |
Wang et al. 2016394 |
Ye et al. 2018395 |
Yilmaz et al. 2005396 |
Yuksel et al. 2015397 |
Zehri et al. 2010398 |
Zhou et al. 2011399 |
References for Appendix 1b.
Stone Clearance for Medical Expulsive Therapy versus Standard of Care in Mid and Proximal Ureter Stones ≤10mm |
Mid Ureteral Stone |
Ibrahim et al. 2013373 |
Itoh et al. 2011375 |
Pickard et al. 2015385 |
Sur et al. 2015391 |
Proximal Ureteral Stone |
Ibrahim et al. 2013373 |
Itoh et al. 2011375 |
Lee et al. 2014400 |
Pickard et al. 2015385 |
Sur et al. 2015391 |
Yencilek et al. 2010401 |
References for Appendix 1c.
Pain Episodes for Medical Expulsive Therapy versus Standard of Care by Stone Location |
Distal Ureteral Stone |
Ahmed and Al-Sayed 2010355 |
Al-Ansari et al. 2010356 |
Albert et al. 2016357 |
Ferre et al. 2009402 |
Griwan et al. 2010370 |
Mshemish 2012381 |
Porpiglia et al. 2009386 |
Sayed et al. 2008389 |
Sen et al. 2017390 |
Vincendeau et al. 2010393 |
Wang et al. 2008403 |
Wang et al. 2016394 |
Yilmaz et al. 2005396 |
Yuksel et al. 2015397 |
Zhou et al. 2011399 |
Proximal Ureteral Stone |
Lee et al. 2014400 |
References for Appendix 1d.
Pain Medication Dosage for Medical Expulsive Therapy versus Standard of Care in Distal Ureteral Stones |
Al-Ansari et al. 2010356 |
Balci et al. 2014404 |
Bashir et al. 2023361 |
Bayraktar and Albayrak 2017362 |
El-Gamal et al. 2012405 |
Falahatkar et al. 2021368 |
Griwan et al. 2010370 |
Hermanns et al. 2009372 |
Itoh et al. 2013376 |
Nuraj and Hyseni 2017383 |
Porpiglia et al. 2006406 |
Porpiglia et al. 2009386 |
Samir et al. 2023388 |
Wang et al. 2016394 |
Ye et al. 2018395 |
Yilmaz et al. 2005396 |
Yuksel et al. 2015397 |
References for Appendix 1e.
Rate of Emergency Department Visits for Medical Expulsive Therapy versus Standard of Care by Stone Location |
Distal Ureteral Stone |
Ahmad et al. 2015354 |
Ahmed and Al-Sayed 2010355 |
Albert et al. 2016357 |
Autorino et al. 2005359 |
El Said et al. 2015407 |
Erturhan et al. 2007367 |
Furyk et al. 2016369 |
Mshemish 2012381 |
Zehri et al. 2010398 |
Proximal Ureteral Stone |
Yencilek et al. 2010401 |
References for Appendix 1f.
Rate of Surgical Intervention for Medical Expulsive Therapy versus Standard of Care |
Ahmed and Al-Sayed 2010355 |
Autorino et al. 2005359 |
Eryildirim 2015408 |
Ferre et al. 2009402 |
Furyk et al. 2016369 |
Georgescu 2015409 |
Hermanns et al. 2009372 |
Lee et al. 2014400 |
Meltzer 2018410 |
Mshemish 2012381 |
Park 2012411 |
Pickard et al. 2015385 |
Sen et al. 2017390 |
Vincendeau et al. 2010393 |
Wang et al. 2016394 |
Yencilek et al. 2010401 |
APPENDIX 2. META-ANALYSIS OF STONE-FREE RATE FOR SWL VERSUS URS, SWL VERSUS PCNL, AND URS VERSUS MINI-PCNL
Appendix 2 References
References for Appendix 2a.
Stone-free rate for URS versus SWL by Kidney Stone Location |
Lower Pole Stones |
Bozzini et al. 2017197 |
Kumar Kumar et al. 2015a412 |
Kumar Nanda et al. 2015b413 |
Pearle et al. 2008118 |
Salem 2013414 |
Schoenthaler et al. 2022415 |
Sener et al. 2014119 |
Sener et al. 2015106 |
Terribile et al. 2019416 |
Zhang et al. 2019122 |
References for Appendix 2b.
Stone-free rate for URS versus SWL by Ureteral Stone Location |
Distal Ureteral Stones |
Adnan et al. 202173 |
Verze et al. 2010194 |
Proximal Ureteral Stones |
Bangash et al. 2020196 |
El-Abd et al. 202283 |
Manzoor et al. 2013193 |
Salem 200976 |
Ur Rehman et al. 2020417 |
References for Appendix 2c.
Stone-free rate for PCNL versus SWL by Location |
Lower Pole Stones |
Albala et al. 2001120 |
Bozzini et al. 2017197 |
Kumar Kumar et al. 2015a412 |
Soliman et al. 2021418 |
Terribile et al. 2019416 |
Yuruk et al. 2010419 |
Zhang et al. 2019122 |
Non-Lower Pole Stones |
Ahmed et al. 2021420 |
Deem et al. 2011421 |
Gadelkareem et al. 2020422 |
Gadelmoula et al. 2019137 |
References for Appendix 2d.
Stone-free rate for URS versus mini-PCNL for 1-2 cm Stones |
Agrawal et al. 2016423 |
Dutta et al. 2023141 |
Jain et al. 2021146 |
Jin et al. 2019148 |
Kumar et al. 2023145 |
Perri et al. 2022147 |
Sajjad et al. 2023424 |
Tang et al. 2023144 |
Ur Rehman et al. 2023142 |
Zeng 2018425 |
References for Appendix 2e.
Stone-free rate for URS versus Standard PCNL for >2 cm Stones |
Bryniarski 2012426 |
Çakıcı 2020427 |
Karakoyunlu 2015151 |
References for Appendix 2f.
Stone-free rate for SWL versus URS |
Adnan et al. 202173 |
Bangash et al. 2020196 |
Bozzini et al. 2017197 |
Dasgupta et al. 202275 |
El-Abd et al. 202283 |
Fankhauser et al. 2021428 |
Islam and Malik 2012429 |
Javanmard et al. 2015123 |
Kumar Kumar et al. 2015a412 |
Kumar Nanda et al. 2015b413 |
Lee et al. 2006430 |
Manzoor et al. 2013193 |
Pearle et al. 2008118 |
Ravier et al. 2015431 |
Salem 200976 |
Salem 2013414 |
Schoenthaler et al. 2022415 |
Sener et al. 2014119 |
Sener et al. 2015106 |
Terribile et al. 2019416 |
Ur Rehman et al. 2020417 |
Verze et al. 2010194 |
Zhang et al. 2011432 |
Zhang et al. 2019122 |
Appendix 3. META-ANALYSIS FOR STONE CLEARANCE USING SWL
Appendix 3 References
References for Appendix 3a.
Stone Clearance using SWL with Shock Rate of 60 per Minute Versus 120 Shocks per Minute |
Ali et al. 2021242 |
Davenport et al. 2006243 |
Madbouly et al. 2005240 |
Moon et al. 2012241 |
Pace et al. 2005244 |
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