Ureteral Stent Placement After Ureteroscopy for Renal Stones: A Randomized Controlled Trial

Vanderbilt University Medical Center103 enrolled

Overview

The rationale for this study is to determine if there is a difference in complications among patients undergoing ureteroscopy for renal stones who receive a stent compared to not receiving a stent postoperatively.

Kidney stones affect 9% individuals within the United States, and the prevalence is increasing. Over the last few decades, ureteroscopy has become the most commonly performed stone procedure. However the complication rate after ureteroscopy is not insignificant. Reducing morbidity after ureteroscopy would improve patient outcomes and reduce health care utilization. A major contributor to patient morbidity after ureteroscopy is the ureteral stent, which is placed at the time of surgery and left in place 1-2 weeks after surgery. The rationale for utilizing stents is to prevent urinary obstruction from edema or stone fragments. On the other hand, stents cause hematuria, pain, and lower urinary tract symptoms. Additionally, stent-related symptoms are often misdiagnosed as urinary tract infections leading to unnecessary antibiotic use. The clinical utility of ureteral stents after ureteroscopy has not been well studied, specifically a stone located in the kidney. Prior studies on stent-less ureteroscopic procedures have focused on treatment of ureteral stones and not stones located in the kidney, have had restrictive inclusion and exclusion criteria, are primarily from single center institutions, and most being performed \~15 years ago. Surgical techniques and device innovations have changed the procedure since that time. To date, there have been only 2 studies that included stone located in the kidney showing no difference in unplanned hospital revisits, however both combined analyses with ureteral stones and selection bias was an issue for both studies. In addition, there is a lack of studies assessing opiate use, impact of quality of life with stent placement, and loss of work related to stent placement

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

103

Conditions

Kidney Calculi

Interventions

UreteroscopyPROCEDURE

Ureteroscopy for 1.5cm or less renal stones.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * nonobstructing renal stone 1.5cm total stone diameter (if multiple stones, then sum of maximum diameters) or less undergoing ureteroscopy Exclusion Criteria: * age \< 18 years * pregnancy status * ureteral stone * preoperative hydronephrosis * indwelling nephrostomy tube * planning bilateral ureteroscopy or subsequent staged ureteroscopy * solitary kidney or eGFR \<60 mL/min (CKD stage 3 or greater) * variant anatomy including horseshoe kidney, pelvic kidney, prior urinary tract reconstruction

Locations (7)

University of California Los Angeles

Los Angeles, California, United States

University of California Davis

Sacramento, California, United States

University of California San Diego

San Diego, California, United States

Indiana University Health Physicians Urology

Indianapolis, Indiana, United States

Outcomes

Primary Outcomes

Total number of complications

Total number of complications - Defined as ER visits related to procedure, unanticipated provider visit, and hospitalization

Time frame: 30 days after ureteroscopy

Secondary Outcomes

PROMIS (Patient-Reported Outcomes Measurement Information System) form 6a

This survey assesses self-reported consequences of pain on relevant aspects of one's life, including engagement with social, cognitive, emotional, physical, and recreational activities. There are 6 questions on the survey. The survey score uses at T-score metric with a mean of 50 and a standard deviation of 10 in a referent population. A higher score denotes greater pain interference in one's life.

Time frame: baseline to 5-10 days after ureteroscopy

WISQOL (Wisconsin Stone Quality of Life Questionnaire)

This is a disease specific quality-of-life instrument designed to assess the impact on patients of stones in the urinary tract. The survey is a 28-item instrument with a 5-point LIkert scale for each item. There are a total of 140 points total, and a difference of 10 points can be considered clinically significant.

Time frame: baseline to 5-10 days after ureteroscopy

Cumulative opiate morphine equivalent dosing (MED)

This will be the calculated morphine equivalent dosage of all opiate medications that are prescribed after surgery to follow-up at 5-10 days.

Time frame: baseline to 5-10 days after ureteroscopy

% return to work

This is the number of participants that have returned to work at the time of follow-up at 5-10 days divided by the total participants in the group.

Time frame: 5-10 days after ureteroscopy

Number of participants with symptomatic urinary tract infection (UTI)

Data from ClinicalTrials.gov

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