| RANDOMIZED
PROSPECTIVE EVALUATION OF NEPHROSTOMY TUBE CONFIGURATION: IMPACT ON POSTOPERATIVE
PAIN
(
Download pdf )
DEREK WEILAND,
RENATO N. PEDRO, J. KYLE ANDERSON, SARA L. BEST, COURTNEY LEE, KARI HENDLIN,
JOHNSTONE KIM, MANOJ MONGA
Department
of Urologic Surgery, University of Minnesota, Minneapolis, USA
ABSTRACT
Objective:
Conduct a prospective randomized single-blind comparison of two nephrostomy
catheter designs, evaluating specifically intraoperative placement and
postoperative comfort.
Materials and Methods: The single-blind,
prospective randomized trial was conducted with institutional review board
approval. All patients undergoing percutaneous nephrolithotomy who gave
informed consent were randomized to placement of either a Boston Scientific
Flexima 8.3F pigtail nephrostomy tube #27-180 (PIG) or a Boston Scientific
8.2F nephroureteral stent #410-126 (NUS). Randomization was concealed
from the surgeon until time of placement. Subjective intraoperative placement
characteristics were rated by the surgeon on a scale of 1 = excellent,
2 = fair, 3 = good and 4 = poor. The patient’s postoperative pain
intensity was evaluated with a Visual Analog Pain Score (0 = no pain to
10 = worst pain).
Results: Nine patients were randomized to
each group. The PIG group was rated significantly better than the NUS
group with regards to ease of placement (p = 0.007) and radiopacity of
the tube (p = 0.007) by surgeon. Visual analog pain scores on postoperative
day one, was significantly lower in the PIG group (mean = 2+/-2) than
the NUS group (mean = 5+/-1) (p = 0.004). The mean amount of intra-venous
morphine equivalent given in the PIG group (mean = 1+/4 Eq morphine) was
less on average compared to the NUS group (mean = 6+/13 Eq morphine),
but the differences did not reach statistical significance (p = 0.06).
Conclusions: Following percutaneous nephrolithotomy,
use of a small pig-tail nephrostomy tube results in greater ease of placement
and less postoperative pain than a nephroureteral catheter.
Key
words: percutaneous nephrolithotomy; postoperative pain; nephrostomy;
stent; randomized controlled trial
Int Braz J Urol. 2007; 33: 313-22
INTRODUCTION
Percutaneous
nephrolithotomy (PCNL) has been the standard of care for large renal calculi
since its introduction in 1976 (1). It has been reported that patients
will require up to 6.5 doses of narcotics postoperative, and the time
to complete recuperation and resumption of full activities is over 9 days
(2,3).
It has been proposed that the degree of
postoperative discomfort corresponds to the size of percutaneous nephrostomy
tube left at the conclusion of the procedure (4). However, while catheter
size may impact patient discomfort, the impact of catheter configuration
on postoperative pain has not been evaluated in a prospective study.
The purpose of this study is to compare
patient discomfort, morbidity and efficacy with two 8F catheters: a pigtail
(Flexima) versus an open-ended nephroureteral catheter for postoperative
renal drainage following PCNL. This study will specifically evaluate the
impact of nephrostomy tube design.
MATERIALS
AND METHODS
This
single-blind, prospective randomized trial was conducted with institutional
review board approval. All patients undergoing percutaneous nephrolithotomy
from January 2005 to March 2006 who gave informed consent were randomized
to placement of either a Boston Scientific Flexima 8.3F pigtail nephrostomy
tube (Flexima copolymers, #27-180) (PIG) or a Boston Scientific 8.2F nephroureteral
stent (Percuflex durometer, #410-126) (NUS). Patients were blinded to
the stent placed for the duration of the study. Simple randomization was
performed using a computer-generated number sequence and was concealed
from the surgeon until time of placement.
All patients undergoing percutaneous nephrolithotomy
during the study period were approached for informed consent to participate.
Patients were excluded if an antegrade endopyelotomy was performed concurrently.
Patients were counseled that if a ureteral injury occurred during the
procedure a nephroureteral stent would be left in place, however this
did not occur during our study.
Placement of each catheter was performed
over the working super-stiff guide-wire, through the lumen of the 30F
Amplatz nephrostomy sheath at the completion of the procedure. The position
of the catheter was confirmed fluoroscopically with the pigtail nephrostomy
catheter positioned in the renal pelvis, while the nephroureteral stent
traversed the ureter with coiling in the bladder. The coils for each catheter
were formed by gentle tension on the retention suture. The catheters were
secured at the skin level with 2-0 silk sutures.
Subjective intraoperative placement characteristics
were rated by the surgeon on a scale of 1 = excellent, 2 = fair, 3 = good
and 4 = poor. The patient’s postoperative pain intensity was evaluated
with a Visual Analog Pain Score (0 = no pain to 10 = worst pain). Narcotic
diaries were maintained and all opioid drugs were converted to a morphine
equivalent (Eq morphine), Table-1.
The present study was powered based on prior
studies of percutaneous nephrostomy size and technique, which have demonstrated
significant differences with sample sizes of 10 patients per arm (4-6).
Student t-test was also used to study the
impact of catheter configuration on pulmonary function (FEV1), blood loss
(Hgb), serum creatinine level (Crt), length of stay, and time to ambulation
and oral food intake (hours). It is relevant to mention that oral fluid
intake was encouraged to commence in the immediate peri-operative recovery
period, and time to oral intake was defined as tolerating oral liquids.
P values < 0.05 were considered significant.
Nephrostomy catheters were clamped on postoperative
day 1 if there were no concerns regarding fever, pain, hematuria or residual
stone fragments. If the patient did not experience pain within 3 hours
of clamping, the catheter was removed by transecting the catheter at the
skin level to release the retention coil.
RESULTS
Nine
patients were randomized to each group. Demographic features of both groups
(gender, stone size, laterality) were comparable except mean age, which
was significantly lower in the NUS than PIG (54 ± 11 versus 65
± 11 years, respectively) (p = 0.004) (Table-2).
The PIG group was rated significantly better
than the NUS group with regards to ease of placement (p = 0.007) and radiopacity
of the tube (p = 0.007) by surgeon (Figure-1).
Visual analog pain scores on postoperative
day one, was significantly lower in the PIG group (mean = 2 ± 2)
than the NUS group (mean = 5 ± 1) (p = 0.004) (Figure-2). The mean
amount of intra-venous morphine equivalent given in the PIG group (mean
= 1, Standard Deviation = 4 Eq morphine) was less on average compared
to the NUS group (mean = 6, Standard Deviation = 13 Eq morphine), but
the differences did not reach statistical significance (p = 0.06). In
the PIG group five of eight patients (62.5%) had their catheters placed
supra-costal versus only 3 of eleven (27.7%) in the NUS group. There was
no significant difference in calyx selected for puncture in the PIG (2
upper, 4 middle and 2 lower) and NUS (3 upper, 2 middle, 6 lower) groups.
The location of puncture did not influence the ease of placement in both
groups.
One patient of NUS group was excluded from
the time to ambulation and PO intake statistical analysis because of a
pulmonary embolus that required rest and fasting for a longer period of
time (120 hours).
PIG group had significant less time (p =
0.005) to PO intake than NUS group (3.7 ± 2.8 hours PIG - 10.88
± 6.19 hours NUS). Neither catheter was superior in regards to
change in Hgb (0.96 ± 0.53 mg/dL NUS, 2.16 ± 0.53 mg/dL
PIG) (p = 0.15); change in Crt (0.047 ± 0.57 mg/dL NUS, 0.14 ±
0.22 mg/dL PIG) (p = 0.20); change in FEV1 (88.9 ± 32.02 mL NUS
- 243.6 ± 119.89 mL PIG) (p = 0.60); length of stay (2.81 ±
1.82 days NUS - 3.15 ± 3.44 days PIG) (p = 0.80); dressing changes
(6.8 ± 5.90 NUS - 3.75 ± 2.90 PIG) (p = 0.38), or ambulation
(17.50 ± 10.53 hours NUS - 9.7 ± 6.0 hours PIG) (p = 0.11)
(Table-3).
COMMENTS
Percutaneous
nephrostomy tubes are associated with postoperative pain and long hospital
stays. The intensity of distress is related to the size of the nephrostomy
catheters. It has been reported that smaller catheters reduce patient
discomfort without increasing procedure morbidity (5).
The issue of stent size (8F vs. 20F or larger)
has already been addressed clearly in the literature (5,6) and currently
our practice is to utilize exclusively an 8F drainage tube after PCNL.
Tubeless PCNL has been shown to be an effective alternative in select
patients (6), though one might debate the relative quality of life issues
related to a PNT vs. ureteral stent left following a tubeless procedure.
Recently, Choi et al. demonstrated in a randomized trial that the post
operative discomfort is similar between small bore nephrostomy tubes and
tubeless PCNL (7). Though convalescence was shorter for the tubeless cohort
in this study, the nephrostomy tube was left in place for 3-5 days, which
exceeds our practice of removing the tube within the first 48 hours if
possible.
In our minds, the remaining issue to resolve
was to determine the optimal configuration of the percutaneous nephrostomy
catheter. Though one might intuitively predict a pigtail catheter would
cause less discomfort, lacking the ureteral and bladder segments, an alternative
view would be that the nephroureteral stent promotes drainage, particularly
in the face of clot or residual stone fragments. Nephrostomy catheter
configuration has previously been demonstrated to impact drainage properties
and retention strength (8).
Whereas scientific reports have analyzed
specifically the size of the PNT and its relationship to postoperative
pain, no study has prospectively compared different types of mini-tubes
of the same size with regards to patient discomfort.
In this study, 18 patients were randomized
and prospectively analyzed regarding severity of pain and opioid intake
after placement of two different 8.3F. Catheters; a pigtail (PIG) and
nephroureteral (NUS) for nephrostomy drainage. Visual analog pain scores
demonstrated that the PIG group had significantly less postoperative pain
than the NUS group (p = 0.04). The same trend was noted with regards to
intra-venous morphine equivalent required by PIG group, which was less
on average than NUS (p = 0.06). Surprisingly, PIG group had a higher incidence
of supra-costal punctures, which would predispose to more pain, therefore
the differences between NUS and PIG may be even more pronounced than noted
in our results.
None of the groups showed significant differences
in blood loss, length of hospital stay, pulmonary function and time to
ambulation; these data are supported by recent reports that present small
bore catheters as a safe and comfortable choice for nephrostomy drainage
(5, 6). Time to PO intake was significantly lower in the PIG group than
the NUS (p = 0.05), which may be linked to the difference in pain described
above.
In addition, both catheters were evaluated
by the urologic surgeons according to the ease of placement and radiopacity.
Although both catheters demanded no great effort in their insertion, the
PIG catheters were found to be easier to manipulate and easier to be visualized
under fluoroscopy than NUS (p = 0.007).
In a different patient population, Mokhmalji
et al. presented a prospective randomized clinical trial comparing quality
of live (QoL) after ureteral (JJ) stent or nephrostomy tube placement
for relief of ureteral obstruction. They demonstrated that reduction in
QoL was moderate but more pronounced in patients with ureteral stents
than in those who underwent percutaneous nephrostomy (9). This study supports
our observation that patient discomfort increases when the drainage catheter
traverses the ureter and bladder; for this reason, we currently use a
nephroureteral stent only in the face of endopyelotomy or ureteral perforation.
In contrast, Karger et al. stated that the
8.5F NUS spared patients of post operative pain compared to a historical
control group comprised of patients with a 24F Malecot nephrostomy tube
(10). This study, however, was not randomized and used catheters of greatly
differing calibers for their comparison; such that the observed differences
could be attributable to catheter size rather than configuration.
One limitation of the present study is that
we did not assess other urinary tract symptoms such as urgency and frequency,
nor did we localize the site of the pain. Nevertheless, as our study evaluates
the impact on post operative pain and morbidity of two catheters of the
same size, the findings suggest that nephrostomy catheter design may play
an important role in patient postoperative comfort.
CONCLUSION
Following
percutaneous nephrolithotomy, use of a small pig-tail nephrostomy tube
results in greater ease of placement and less postoperative pain than
a nephroureteral catheter.
CONFLICT
OF INTEREST
The research was supported by Boston Scientific.
REFERENCES
- Fernstrom I, Johansson B: Percutaneous pyelolithotomy. A new extraction
technique. Scand J Urol Nephrol. 1976; 10: 257-9.
- Rittenberg MH, Koolpe H, Keeler L, McNamara T, Bagley DH: Pain control:
comparison of percutaneous and operative nephrolithotomy. Urology. 1985;
25: 468-71.
- Netto NR Jr, Lemos GC, De Almeida Claro JF, Palma PC: Comparison
between percutaneous nephrolithotomy and open stone procedures. Int
Urol Nephrol. 1988; 20: 225-30.
- Maheshwari PN, Andankar MG, Bansal M: Nephrostomy tube after percutaneous
nephrolithotomy: large-bore or pigtail catheter? J Endourol. 2000; 14:
735-7; discussion 737-8.
- Pietrow PK, Auge BK, Lallas CD, Santa-Cruz RW, Newman GE, Albala
DM, et al.: Pain after percutaneous nephrolithotomy: impact of nephrostomy
tube size. J Endourol. 2003; 17: 411-4.
- Desai MR, Kukreja RA, Desai MM, Mhaskar SS, Wani KA, Patel SH, et
al.: A prospective randomized comparison of type of nephrostomy drainage
following percutaneous nephrostolithotomy: large bore versus small bore
versus tubeless. J Urol. 2004; 172: 565-7.
- Choi M, Brusky J, Weaver J, Amantia M, Bellman GC: Randomized trial
comparing modified tubeless percutaneous nephrolithotomy with tailed
stent with percutaneous nephrostomy with small-bore tube. J Endourol.
2006; 20: 766-70.
- Canales BK, Hendlin K, Braasch M, Antolak C, Reddy A, Odeh B, et
al.: Percutaneous nephrostomy catheters: drainage flow and retention
strength. Urology. 2005; 66: 261-5.
- Mokhmalji H, Braun PM, Martinez Portillo FJ, Siegsmund M, Alken P,
Kohrmann KU: Percutaneous nephrostomy versus ureteral stents for diversion
of hydronephrosis caused by stones: a prospective, randomized clinical
trial. J Urol. 2001; 165: 1088-92.
- Kader AK, Finelli A, Honey RJ: Nephroureterostomy-drained percutaneous
nephrolithotomy: modification combining safety with decreased morbidity.
J Endourol. 2004; 18: 29-32.
____________________
Accepted after revision:
March 16, 2007
_____________________
Correspondence address:
Dr. Manoj Monga
Department of Urologic Surgery
University of Minnesota
Mayo 394, 420 Delaware St. SE
Minneapolis, MN, 55455, USA
Fax: + 1 612 624-4430
E-mail: endourol@yahoo.com
EDITORIAL COMMENT
The era of open stone surgery and plastic surgical correction of the renal
pelvis, beside the unavoidable trauma of open surgical access had already
been dominated by postoperative problems regarding drainage systems and
urinary reduction.
Postoperative problems due to different
percutaneous and/or intraluminal catheters basically are induced by the
following factors: affection of the respiratory system caused by transpassing
catheters, affection of the percutaneous stent location because of the
renal mobility, suppression of the peristaltic activity inside the collecting
system caused by the”foreign bodies”, decline in reflux –
protection caused by ureteral stents entering the bladder and passing
Waldeyers sheet.
The effect on patients postoperative condition
means additional multiple branch therapy, i.e. analgesic regimen, treatment
of ascending infections, prolongation of the hospital stay and an increase
in costs as well.
The urological progress of the last decade
especially with minimally invasive procedures and also minimal percutaneous
nephrolithotripsy (PCNL) induced effective research and investigations
to minimize the postoperative drainage related trauma, what has also been
demonstrated by the present article, culminating in the tubeless postoperative
nephrostomy using the pouring effect of gelatine to perform a watertight
closure of the working channel.
The very actual status of the investigations
demands for obligatory strategies and roules also for drainage systems
after PCNL dependant on residual clearance function, stone history (number,
size, consistency ), infectious conditions, duration of the surgical procedure
and patients complication level value.
Dr.
Volker Schick
Urologische Abteilung
Robert Koch-Krankenhaus
Gehrden, Germany
E-mail: schick@rkk-gehrden.de
EDITORIAL COMMENT
One of the most
significant areas of investigation with regards to percutaneous nephrolithotomy
(PCNL) involves the need for, and type of drainage of the collecting system
with a percutaneous nephrostomy catheter. Postoperative discomfort from
a percutaneous catheter placed at the conclusion of the procedure has
been attributed to a number of factors including catheter diameter, access
location, and number of catheters. Many surgeons have been revising their
technique in favor of placing smaller catheters or performing tubeless
PCNL, with the intention of reducing patient discomfort without compromising
procedural outcomes or increasing complications.
The purpose
of this study was to prospectively examine the impact of percutaneous
catheter design on postoperative pain following PCNL. Specifically, an
8.3F pigtail nephrostomy catheter (PIG) was compared to an 8.2F open-ended
nephroureteral catheter (NUS). The authors conclude that the PIG was less
painful than the NUS, based on lower visual analog pain scores and lower
analgesic requirements. Increased pain in the NUS group was thought to
be due to the catheter traversing the ureter and bladder. This idea has
been previously proposed in studies comparing the discomfort associated
with a percutaneous nephrostomy catheter as compared to an indwelling
ureteral stent in the setting of obstruction.
The authors
should be applauded on their efforts in conducting this evaluation, however
several limitations are apparent. There is a statistically significant
difference in ages between the two groups, as the mean age of the NUS
group was 11 years younger than the PIG group. Pain thresholds between
individuals of different ages can vary considerably and may impact reporting
of pain scores. The authors state that both catheters demanded no great
effort in their insertion, although the PIG group was subjectively rated
better in terms of ease of catheter placement. The authors did not cite
a reason for this observation. If this is the case, then one might conclude
that more difficult catheter insertion in the NUS group may translate
into greater postoperative discomfort.
While there
was no significant difference in selection of calyceal puncture between
the groups, 62.5% of catheters in the PIG group were supracostal, compared
to only 27.7% in the NUS group. It is surprising to note that despite
a higher number of supracostal catheter placements in the PIG group, the
pain scores were lower than in the NUS group. This would suggest that
the location of the access does not correlate with the amount of discomfort.
The authors appropriately acknowledge that they did not localize the location
of pain in either group. This point is extremely important, since pain
in the NUS group may be compounded by ureteral and bladder irritation.
Without this information, it may be conceivable that even the suture securing
each catheter to the skin, may somewhat contribute to the degree of discomfort.
In summary,
nephrostomy tube configuration does appear to directly impact postoperative
pain. Based on the results provided by the authors, additional studies
with larger matched cohorts would serve to validate the conclusions of
this study.
Dr. Ravi
Munver
Chief, Minimally Invasive Urologic Surgery
Director, Endourology Fellowship Program
Hackensack University Medical Center
Hackensack, New Jersey, USA
E-mail: rmunver@humed.com
EDITORIAL COMMENT
In
this prospective randomized trial, the authors evaluated the impact of
percutaneous tube configuration (8.3F pigtail nephrostomy tube vs. 8.2F
nephroureteral stent) on pain scores at postoperative day-1 and the ease
of intraoperative tube placement following percutaneous nephrolithotomy
(PCNL) in a total of 18 patients. There were nine patients in each arm.
The pigtail group was associated with easier tube placement and better
visualization on fluoroscopy (subjective evaluation by the surgeon). Furthermore,
patients who received pigtail nephrostomy tubes had marginally less analgesia
requirements (morphine equivalent) and their pain scores were significantly
lower. There was no statistical difference between the two groups regarding
the change in hemoglobin and creatinine levels, change in pulmonary function,
time to ambulation, and hospital stay. However, patients in the pigtail
group resumed oral intake earlier. On the basis of their findings, the
authors concluded that the use of an 8.3F pigtail nephrostomy tube following
PCNL resulted in greater ease of placement and less postoperative pain
than an 8.2F nephroureteral catheter.
The
efficacy and safety of PCNL for the treatment of kidney stones greater
than 2 cm in diameter in upper and middle calices, and greater than 1
cm in diameter in lower calices, is well established. The ideal drainage
method following PCNL is of interest, because it is intimately related
to the patients’ quality of life and length of hospital stay. Currently,
there is a trend towards the use of the “tubeless” technique
(involving the placement of a ureteral stent instead of a nephrostomy
tube) or the use of small bore nephrostomy tubes. Several points relating
to the complexity of the procedure, status of the affected kidney, and
body habitus of the patient need to be considered before choosing the
ideal tube following PCNL. The “tubeless” technique may be
appropriate in select patients, such as those with small stone burdens,
no significant intraoperative complications and no significant residual
stones (1). As such, presence of an intraoperative complication such as
significant hemorrhage or perforation, or residual stones mandates placement
of a nephrostomy tube. The “tubeless” technique raises concerns
that the risk of bleeding and urinary extravasation may be increased.
Moreover, the concurrent morbidity of stents should not be underestimated.
Additionally, patients with severe hydronephrosis are likely to benefit
from the nephrostomy tubes. Lastly, obese patients may suffer from dislodging
of the pigtail tubes resulting from pannus movement.
However,
“tubeless” PCNL appears to reduce postoperative morbidity.
Therefore, it would be useful to examine adjunctive methods that would
augment the efficacy and safety of this technique. For example, gelatin
matrix thrombin has been used to seal PCNL tracts in small patient series
with favorable preliminary results. Lee at al. (2) first described the
use of gelatin matrix thrombin in PCNL tracts. However, to date, a prospective
randomized trial does not exist in the published literature assessing
the true role of hemostatic agents and/or urinary sealants for PCNL tract
closure.
As
the authors stated, nephroureteral stents may promote more efficient urinary
drainage compared to pigtail tubes. Traditionally, drainage after PCNL
has been achieved with large bore re-entry tubes to provide effective
pelvi-ureteric junction stenting, tamponade of the PCNL tract, preservation
of ureteric access, and allow repeat access for a “second look”
PCNL if required. However, the current data supports the use of small
bore tubes following uncomplicated PCNL (references 4 - 6 in the article).
Desai et al. proposed an algorithm for nephrostomy drainage after PCNL
based on their large experience and findings of their prospective randomized
trial comparing the three different drainage methods (reference 6 in the
article). In brief, the authors recommend the use of a large bore (20F)
nephrostomy tube following complicated PCNL, and either a 6F double-J
stent (if stone-free) or a small bore (9F) nephrostomy tube (if residual
stones) following uncomplicated PCNL. Another drainage strategy was proposed
by Kim et al. after PCNL for large or complex stones (3). In the presence
of pyonephrosis, large residual stones and/or difficult renal anatomy,
a 20F re-entry tube was recommended. If multiple accesses were required
then a 20F circle loop was suggested and an 8.5/10F cope loop was recommended
after a standard PCNL.
The
authors should be commended for conducting a prospective randomized trial.
However, some pertinent issues deserve attention. Ideally, it would be
natural to expect a detailed inclusion and exclusion criteria from a prospective
study protocol. Secondly, the impact of nephrostomy tube size on stone-free
rates with small residual stones after PCNL is not well addressed. From
this perspective, it would be useful to know the stone-free rates after
PCNL in the current study as well as in future studies on this topic.
More importantly, evaluation of the impact of stent/tube diameter or configuration
on the patients’ quality of life, as assessed by validated questionnaires,
would undoubtedly provide more objective and structured analysis. For
instance, Joshi et al. developed and validated the ureteral stent symptom
questionnaire (USSQ) for symptom and quality of life evaluation to assess
the impact of different types of stents (4). Finally, the sample size
estimation for this study does not appear to be based on the primary outcome
of interest and the method of power calculation has not been thoroughly
described. The only prior study of the three referenced by the authors
for power calculation, that has assessed pain as a primary end-point,
recruited 30 patients. Therefore, it is likely that this current study
in which 18 patients were recruited was under-powered. Fortunately, the
authors found some significant results. The authors reported, for most
variables, the means and standard deviations, and used t-tests for data
analysis. Medians and inter-quartile ranges (IQR) are more appropriate
to avoid small means with meaningless negative standard deviations, e.g.,
IV morphine equivalent with mean = 1 and SD = 4. For a study with only
9 patients in each of the two arms, it is important to check assumptions
by using t-tests primarily assessing the normality assumption for the
continuous variables. Alternatively, nonparametric methods, such as a
Wilcoxon test, can be used. Even though this is a randomized study, patient
age was different between the two arms. That alone may render the significant
difference in the primary outcome artificial.
Notwithstanding
these caveats, the current study adds information to the literature with
some objective evidence to support the role of small bore pigtail nephrostomy
tubes after percutaneous nephrolithotomy in order to reduce operative
morbidity.
REFERENCES
- Bellman
GC, Davidoff R, Candela J, Gerspach J, Kurtz S, Stout L: Tubeless percutaneous
renal surgery. J Urol. 1997; 157: 1578-82.
- Lee DI,
Uribe C, Eichel L, Khonsari S, Basillote J, Park HK, et al.: Sealing
percutaneous nephrolithotomy tracts with gelatin matrix hemostatic sealant:
initial clinical use. J Urol. 2004; 171: 575-8.
- Kim SC,
Tinmouth WW, Kuo RL, Paterson RF, Lingeman JE: Using and choosing a
nephrostomy tube after percutaneous nephrolithotomy for large or complex
stone disease: a treatment strategy. J Endourol. 2005; 19: 348-52.
- Joshi
HB, Newns N, Stainthorpe A, MacDonagh RP, Keeley FX Jr, Timoney AG:
Ureteral stent symptom questionnaire: development and validation of
a multidimensional quality of life measure. J Urol. 2003; 169: 1060-4.
Dr. Burak Turna
Department of Urology
Ege University School of Medicine
Izmir, Turkey
E-mail: burakturna@gmail.com
REPLY BY THE AUTHORS
We
appreciate the constructive editorial comments of the expert reviews,
and would like to clarify the following points. All patients undergoing
single access PCNL were offered informed consent - there were no exclusion
or inclusion criteria. The USSQ is validated specifically for ureteral
stents; it has not been validated for percutaneous nephrostomy tubes.
All studies referenced for the power analysis used postoperative pain
as a primary endpoint. The one study that randomized 30 patients (ref.
6 in the article) had 10 patients in each arm (large-bore, small-bore,
tubeless).
|