To Compare the Eectiveness of Percutaneous Nephrostomy
invasive nature and greater comfort of internal signicant bleeding, or painful trigonal irritation.
stenting.9,10 Prospective data from South Asian Successful decompression was assessed clinically and
populations remain limited despite dierences in case by documented relief of obstruction after the index
mix, stone burden, and resource availability. This procedure. Procedural failure included the inability to
prospective cohort study was conducted at a tertiary place the intended drainage device or the need for
care center to compare the short-term eectiveness of immediate alternative diversion. The study protocol
percutaneous nephrostomy and double-J stenting in was approved by the Institutional Research and Ethical
patients with obstructive uropathy and to evaluate Review Board of Khyber Medical College/Khyber
which approach provides more reliable early Teaching Hospital on April 18, 2025. Written informed
decompression in routine clinical practice.
consent was obtained from all participants, and patient
confidentiality was maintained throughout the study.
Patients were screened in the outpatient and emergency
departments. Baseline data were recorded on
structured proforma, including age, sex, side of
obstruction, clinical presentation, and relevant
METHODOLOGY
a
This prospective cohort study was conducted in the
Department of Urology, Khyber Teaching Hospital,
Peshawar, from April 23, 2025, to December 2025.
Patients with newly diagnosed obstructive uropathy
were enrolled during the study period. As treatment
selection was based on clinical decision-making rather
than random allocation, the study design was
observational. The sample size was calculated to detect
examination ndings.11 Laboratory evaluation included
complete blood count, renal function tests, urine
analysis, coagulation prole, and viral markers.
Ultrasonography was used to conrm hydronephrosis
and the aected side. The underlying etiology of
obstruction, infection status at presentation, and grade
of hydronephrosis were recorded from the clinical and
imaging assessment, where available in the patient
record. In the double-J stent group, patients underwent
retrograde ureteral stent placement under cystoscopic
guidance using a 5 to 6 Fr stent. Local anesthesia with
2% lignocaine gel, with or without mild sedation, was
a
clinically meaningful dierence in treatment
effectiveness between the two procedures. Assuming
percutaneous nephrostomy eectiveness of 92% and
double-J stenting eectiveness of 83%, with 80%
power and a two-sided alpha of 0.05, the required
sample size was 416 patients, with 208 patients per
group.11 Consecutive non-probability sampling was
used. All eligible patients presenting during the study
period were considered for inclusion until the required
sample size was achieved. Patients were allocated to
either the percutaneous nephrostomy or the double-J
stent group based on the treating urologist's clinical
judgment, anatomical feasibility, and procedural
suitability. The age between 20 and 80 years and newly
used
according
to
procedural
requirements.
Prophylactic intravenous antibiotics were administered,
and a Foley catheter was retained for 48 hours when
indicated. In the percutaneous nephrostomy group,
patients underwent ultrasound-guided placement of an 8
Fr nephrostomy tube in the prone position under local
inltration with 1% lignocaine. The tube was connected
to an external drainage bag. Peri-procedural antibiotics
were administered according to unit protocol. All
patients were followed for 15 days after the index
procedure. During follow-up, treatment eectiveness
and early complications were recorded, including
procedural failure, septicemia, signicant bleeding, and
painful trigonal irritation. Data were analyzed using
SPSS version 22. Continuous variables, including age,
procedure duration, and hospital stay, were expressed
as mean ± standard deviation. Categorical variables,
including sex, side of obstruction, and treatment
effectiveness, were presented as frequencies and
percentages. Group comparisons were performed using
the independent-samples t-test for continuous variables
and the chi-square test for categorical variables.
Multivariable logistic regression was performed to
adjust for potential confounding. The primary outcome
variable was treatment success at 15 days. The
treatment group was the main predictor variable.
Covariates included age, sex, etiology of obstruction,
diagnosed
obstructive
uropathy
conrmed
on
ultrasonography and ank pain with a visual analog
scale (VAS) score greater than 5 were included. The
Prior surgical or endoscopic intervention for the current
obstructive
episode,
Severe
or
uncorrected
coagulopathy, Uremia secondary to bladder outlet
obstruction as the primary cause, and Bladder outlet
obstruction
from
benign
prostatic
hyperplasia.
Operational denitions included: Obstructive Uropathy:
Defined as a structural or functional obstruction to
urinary ow with hydronephrosis conrmed on
ultrasonography. Percutaneous Nephrostomy (PCN):
Ultrasound-guided placement of an 8 Fr nephrostomy
tube into the renal pelvis for external drainage. Double-
J (DJ) Stent: Cystoscopic-guided retrograde placement
of a ureteral stent. Stent size was 5 or 6 Fr.
Polyurethane stents were used. Local anesthesia with
2% lignocaine gel was administered. Treatment
eectiveness: Successful decompression at 15-day
follow-up without procedural failure, septicemia, hydronephrosis grade, pre-operative urine culture
April - June 2026
J Gandhara Med Dent Sci
66