Evaluation of Retrograde Intrarenal Surgery Results and Stone-free Rate in Children With Kidney Stones

Sponsor
Ankara City Hospital Bilkent (Other)
Overall Status
Completed
CT.gov ID
NCT06138704
Collaborator
(none)
105
1
58
1.8

Study Details

Study Description

Brief Summary

There is a global increase in the prevalence of urolithiasis in children attributed to lifestyle changes, dietary habits, climate changes, childhood obesity, and the wider availability of ultrasonography. The rising incidence of the disease with its recurrent nature emphasizes the need for minimally invasive therapeutic options. Patients in whom RIRS has been performed in the last four years with increasing experience will be presented, and complications, stone-free rates, and technical details will be discussed.

This retrospective Cohort study included children who underwent RIRS. Medical history, serum electrolytes, midstream urine culture, urinalysis, serum creatinine, complete blood count, and coagulation assessments were performed preoperatively. Ultrasonography (USG) was performed three months, 6 months, and 1 year after the procedures to evaluate stone recurrence and hydronephrosis. We analyzed the stone-free rate ,complications, and the conversion to open procedure

Condition or Disease Intervention/Treatment Phase
  • Procedure: Retrograde Intrarenal Surgery

Detailed Description

There has been a worldwide rise in the prevalence of urolithiasis in children, which is linked to changes in lifestyle and dietary habits, climate changes, childhood obesity, and the increased availability of ultrasonography (1). In pediatric stone disease, it is crucial to evaluate the underlying reasons, which may include metabolic disorders, anatomical anomalies, and infection, to avoid higher recurrence of stones after treatment (2). The increasing incidence and recurrence of this disease highlights the necessity for minimally invasive therapeutic solutions. Retrograde intrarenal surgery (RIRS) is gaining new indications owing to advanced laser and endoscopic technology, resulting in a constant rise in the number of procedures (3).

Routine RIRS has been performed in our clinic for the last 15 years with increasing rates. Patients in whom RIRS has been performed in the last three years with increasing experience will be presented, and complications, stone-free rates, and technical details will be discussed.

This retrospective cohort study included children who underwent RIRS between January 2019 and December 2022 at the Ankara Bilkent City Hospital, University of Health Science, Ankara, Turkey. The inclusion criteria were pediatric patients with kidney stones who underwent RIRS. The exclusion criteria were cases that were converted to open surgery, cases in which RIRS could not be performed because of anatomical reasons, and cases in which lower pole stones could not be reached with RIRS. The Ethics Committee of the Institution approved this study (E2-23-5305). All patient details were identified, and all patients provided written informed consent to participate in the study. Medical history, serum electrolytes, midstream urine culture, urinalysis, serum creatinine, complete blood count, and coagulation assessments were performed preoperatively. Plain abdominal film and ultrasonography/computer tomography scan examinations were also performed. Patients with preoperative positive urine culture results received a complete course of culture-specific antibiotics before RIRS Prophylactic antibiotic treatment with cephazolin was administered to all patients prior to surgery.

Surgical treatment was indicated when there was an obstruction, infection, failure of spontaneous stone passage, or stones larger than 7 mm and in the presence of increasing or unremitting colic.

All RIRS procedures were performed under general anesthesia with direct videoscopic and fluoroscopic guidance. All procedures were performed by the same surgeon. Semirigid ureteroscopy (4.5 Fr R. Wolf, Knittlingen, Germany) or flexible ureteroscopy (Karl Storz FLEX-X, Tuttlingen, Germany) was performed to place an access sheath. The decision to use a flexible or semirigid ureteroscope depended on the location of the stones. A flexible ureteroscope was used for lower pole stone, wherease a semirigid ureteroscope was preferred for renal pelvic or upper pole stones. In our practice, all children undergoing RIRS for stone disease received cephazolin. Perioperative antibiotic treatment was continued for a week following surgery. If a double J (JJ) stent was inserted, antibiotic prophylaxis was continued and ceased after removal of the JJ stent. A manual irrigation pump system was used for hydrodilation of the ureter during ureterorenoscopy. If this was not enough to pass the ureteroscope, we placed a JJ catheter for passive dilatation. Ureteral active coaxial or balloon dilation was not performed. We used isotonic fluid at body temperature to avoid hypothermia and hyponatremia during the procedures. The urinary bladder was maintained at low pressure with a 14-F suprapubic angiocatheter in all patients. Stones were fragmented using a holmium-YAG laser (Litho Quanta System, Italy) and grasped by a stone basket when applicable. Contrast injection was performed at the end of the procedures to confirm the absence of extravasation and stone-free status. The decision to place a postoperative uretral stent was made according to visible mucosal ureteral trauma or edema at the end of the procedure. The extracted stone specimens were submitted for stone analysis. All patients were discharged if fever was not detected the day after the procedures. Medical therapy and dietary planning were provided postoperatively on the basis of the composition of the stones. Ultrasonography (USG) was performed three months, six months, and one year after the procedures to evaluate stone recurrence and hydronephrosis. We analyzed the stone-free rate, complications, and conversion to the open procedure. Statistical analysis was performed using the Chi-Square and ANOVA tests, p: 0.05 was considered statistically significant.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
105 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Retrograde Intrarenal Surgery Results and Stone-free Rate in Children With Kidney Stones
Actual Study Start Date :
Jan 1, 2019
Actual Primary Completion Date :
Dec 31, 2022
Actual Study Completion Date :
Oct 31, 2023

Outcome Measures

Primary Outcome Measures

  1. Determination of stone-free rate in children who underwent lithotripsy with retrograde intrarenal surgery for kidney stones. [USG evaluation was performed postoperative 1. month, 3-6-12-18 months, and kidney stones of the patients were evaluated.]

    After the RIRS, patients were monitored with USG in the first month, 3-6-12 months, and stone-free rates were determined.

Secondary Outcome Measures

  1. How long does it take for renal stones to be cleared after RIRS? [USG evaluation was performed postoperative 1. month, 3-6-12-18 months, and kidney stones of the patients were evaluated.]

    Patients first month after RIRS, 3-6-12. It was determined by follow-up with USG over the months and when stone-free status was achieved.

  2. Determination of factors affecting stone-free rate in pediatric patients who underwent RIRS due to kidney stones. [USG evaluation was performed postoperative 1. month, 3-6-12-18 months, and kidney stones of the patients were evaluated.]

    The effects of gender, age, number of stones, presence of staghorn stones, and whether a JJ stent was placed before the procedure on stone-free rates were evaluated in pediatric patients who underwent RIRS due to kidney stones.

  3. Determining the need for repeated interventions to ensure stone-free status [Evaluating 4-year hospital records of patients]

    The presence of additional interventions to ensure stone-free status was evaluated from hospital records.

Other Outcome Measures

  1. Determination of procedure-related complications in pediatric patients who underwent RIRS due to kidney stones. [Evaluating 4-year hospital records of patients]

    Determination of procedure-related complications in pediatric patients who underwent RIRS due to kidney stones.

Eligibility Criteria

Criteria

Ages Eligible for Study:
3 Months to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • The inclusion criteria were pediatric patients with kidney stones who underwent RIRS.
Exclusion Criteria:
  • The exclusion criteria were cases that were converted to open surgery, cases in which RIRS could not be performed because of anatomical reasons, and cases in which lower pole stones could not be reached with RIRS.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ankara Bilkent City Hospital Ankara Turkey

Sponsors and Collaborators

  • Ankara City Hospital Bilkent

Investigators

  • Study Director: Huseyin T Tiryaki, MD, University of Health Science Ankara Bilkent City Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ankara City Hospital Bilkent
ClinicalTrials.gov Identifier:
NCT06138704
Other Study ID Numbers:
  • E2-23-5305
First Posted:
Nov 18, 2023
Last Update Posted:
Nov 18, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ankara City Hospital Bilkent
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 18, 2023