PEDIATRIC UROLOGY
PROSPECTIVE COMPARISON AND 1-YEAR FOLLOW-UP OF
DEXTRANOMER/HYALURONIC ACID COPOLYMER INJECTION
FOR TREATMENT OF VESICOURETERAL REFLUX IN CHILDREN
J. OSWALD, M. RICCABONA, L. LUSUARDI, G. BARTSCH, AND C. RADMAYR
ABSTRACT Objectives. To compare, in a prospective study, the efficacy of a single injection of polydimethylsiloxane (Macroplastique) or dextranomer/hyaluronic acid copolymer (Deflux), a new biodegradable substance, and to assess the short-term and 1-year clinical effects concerning reflux resolution and the safety of these two bulking agents. Subureteral injection of bulking agents has recently demonstrated good success rates for endoscopic treatment of vesicoureteral reflux. Macroplastique has been one of the most popular bulking agents during the past years. Nevertheless, considering the synthetic property, new biodegradable sub- stances have become more relevant. Methods. From January 2000 to June 2001, 16 boys and 56 girls (total of 114 ureters) with a mean age of 34.5 months were treated endoscopically for vesicoureteral reflux. A single subureteral Macroplastique or Deflux injection was performed in 34 children (58 ureters) and 38 children (56 ureters), respectively. Both groups were comparable in terms of baseline parameters. Vesicoureteral reflux was grade II in 52, grade III in 57, and grade IV in 5 ureterorenal units. The procedure was performed on an outpatient basis, with the children under general anesthesia. In addition to the routine parameters, the follow-up evaluation consisted of renal ultrasonography and voiding cystourethrography at 3 and 12 months postoperatively. Results. Endoscopic treatment was performed without any complications in all cases. At the 3-month follow-up visit, reflux was corrected in 50 (86.2%) of 58 refluxing ureters in the Macroplastique group and in 40 (71.4%) of 56 refluxing ureters in the Deflux group. At 1 year of follow-up, reflux correction was maintained in 80.9% of ureters in the Macroplastique group and in 67.6% of ureters in the Deflux group. No postoperative complications were observed in either group. Conclusions. A single subureteral injection of either polydimethylsiloxane (Macroplastique) or dextrano- mer/hyaluronic acid copolymer (Deflux) is an effective treatment modality for children with vesicoureteral reflux. The procedure was well tolerated, safe, and associated with low morbidity. Deflux, a new biocom- patible, biodegradable substance, seems to be an alternative modality to other bulking agents for treating vesicoureteral reflux in children, with acceptable short-term and 1-year results. UROLOGY 60: 894–898, 2002. 2002, Elsevier Science Inc. The conservative treatment of children with urinary tract infections to minimize the risk of re-
vesicoureteral reflux using long-term antibi-
nal scarring and possible long-term consequen-
otic prophylaxis aims to prevent reflux-associated
ces.1,2 This treatment modality relies on the spon-taneous resolution of reflux, which may take years. Additionally, excellent compliance is necessary
From the Department of Urology, University of Innsbruck, Inns-bruck; and Department of Pediatric Urology, KH Barmh Schwest-
and requires long-term surveillance with interven-
ing voiding cystourethrograms. Continuous anti-
Reprint requests: C. Radmayr, M.D., Department of Urology,
biotic prophylaxis is difficult to monitor and is as-
University of Innsbruck, Anichstrasse 35, Innsbruck A-6020,
sociated with increasing compliance problems, as
Submitted: March 11, 2002, accepted (with revisions): June 4,
well as the risk of developing antibiotic resis-
tance.3,4 Approximately one third of children
894 ALL RIGHTS RESERVED
treated nonoperatively will be lost to follow-up and
TABLE I. Distribution of reflux grades before
will remain untreated after medical treatment has
treatment
been started.5,6 Therefore, increasing numbers ofparents prefer endoscopic treatment to avoid long-
VUR Grade Macroplastique (n) Deflux (n)
term antibiotic management. Pediatric urologists
generally agree that an injectable biomaterial can
be an effective way to correct reflux, although the
ideal agent has not yet been identified.7,8 Endo-
scopic treatment is based on the principle of creat-
KEY: VUR ϭ vesicoureteral reflux.
ing a solid support behind the intravesical ureter,elongating the intramural length of the ureter.9,10Hence, the injectable biomaterial must be stable
daily) was administered to all patients. The preoperative urine
without migration and should be encapsulated by
fibrous tissue within a short time. Therefore, poly-dimethylsiloxane (Macroplastique) is one of the
METHODS
most popular bulking agents fulfilling these crite-
The treatment was performed as an outpatient procedure.
ria and is used extensively in medical applications,
The ureteral orifices were visualized using the pediatric 9.5F
especially for endoscopic management of vesi-
Wolf cystoscope with a 5F working channel. A flexible 5F
coureteral reflux.11 Macroplastique consists of
pediatric endoscopic needle prepared with EZ-Gel surgicallubricant was used with the Macroplastique Administration
fully vulcanized solid polydimethylsiloxane parti-
Gun, and a 3.5F polytetrafluoroethylene-coated needle was
cles (40% of volume) in a bio-excretable hydrogel
used to inject dextranomer/hyaluronic acid copolymer (De-
carrier (non-iodine povidone). Macroplastique has
flux) as described previously.20 A single endoscopic subu-
good bulking properties, requiring less material,
reteral Macroplastique or Deflux injection was performed in
with limited or nonexistent migration of the com-
58 and 56 ureters with grade II to IV vesicoureteral reflux,respectively. The differences in the injected volumes between
paratively large, inert microparticles (median min-
the two groups were not statistically significant (Macroplas-
imal diameter 140 m) created as an elas-
tique: range 0.6 to 1 mL, mean 0.8; Deflux: range 0.5 to 1 mL,
tomer.12–14 In 1995, the first experimental and
mean 0.7; P Ͼ0.05). Bilateral reflux was present in 24 children
short-term results of a new bioimplant were pub-
in the Macroplastique group and in 18 children in the Deflux
lished.15 This new biodegradable substance (De-
group. One week after the injection, control renal ultrasonog-raphy was performed to recognize urinary obstruction. Void-
flux) consists of dextranomer microspheres in a
ing cystourethrography (VCUG), ultrasonography, and urine
sodium hyaluronan solution and may serve as a
culture were done in all patients 3 months after discharge. The
new alternative to Macroplastique for the endo-
routine parameters, including medical history, physical con-
scopic treatment of reflux.16 The Deflux system
dition, and adverse events, were recorded at 3 and 12 months
represents a new biocompatible material without
of follow-up. Successful reflux correction was defined as ab-sent or grade I reflux on follow-up VCUG and no de novo
immunogenic properties and a lack of distant mi-
hydroureteronephrosis on renal ultrasonography. At 12
gration.17 In our prospective study using a single
months of follow-up, VCUGs were available for only 24 pa-
injection of either substance, we compared the ef-
tients in the Macroplastique and only 22 in the Deflux group.
ficacy of these two agents for the endoscopic treat-
Antibiotic prophylaxis was stopped if vesicoureteral reflux
ment of reflux in children. The short-term and
was absent or grade I. If reflux persisted, repeated treatmentwith the previous bulking agent was offered to the parents.
1-year clinical effects concerning reflux resolutionand safety were evaluated. STATISTICAL ANALYSIS
The Z test for significance of a single proportion (normal
MATERIAL AND METHODS
test, two sided) was applied for statistical analysis, with deter-mination of confidence intervals of the proportion of positive
PATIENTS
outcomes at 3 months after the procedure for patients treated
Children with vesicorenal reflux were randomly assigned to
the two groups. During the 18-month study period, 72 chil-dren (16 boys and 56 girls) with 114 ureterorenal units un-
derwent subureteral injection of Macroplastique (34 children;24 girls and 10 boys; mean age 33 months) or Deflux (38
All procedures were performed as planned on an
children; 32 girls and 6 boys; mean age 36 months). The reflux
outpatient setting under general anesthesia with
grades were grade II in 52, grade III in 57, and grade IV in 5
no intraoperative complications. At 3 months of
(Table I), according to the reflux grading system recom-mended by the International Reflux Study.18 The exclusion
follow-up, reflux was corrected in 50 (86.2%) of
criteria were duplicated refluxing ureters, Hutch diverticu-
the 58 ureteral units in the Macroplastique group
lum, failed surgical reimplantation, neurogenic bladder deter-
and in 40 (71.4%) of the 56 ureteral units in the
mined by history and multichannel urodynamics, and voiding
Deflux group (Table II). The confidence intervals
dysfunction diagnosed by history and uroflowmetry with sur-
of the proportion of positive outcomes after 3
face electromyography in children with bladder control.19 An-tibiotic prophylaxis using either trimethoprim (1 to 2 mg/kg
months are shown in Figure 1. At the 95% confi-
daily) or co-trimoxazole (sulfamethoxazole 5 to 10 mg/kg
dence interval, no statistically significant differ-
UROLOGY 60 (5), 2002
been seen in either group to date. Two children
TABLE II. Reflux resolution (ureters) after a
after Macroplastique injection and three after De-
single injection
flux injection underwent bilateral repeated injec-
VUR Grade Macroplastique (n) Deflux (n) KEY: VUR ϭ vesicoureteral reflux.
The debate about the ideal bulking agent in en-
doscopic therapy for children with vesicoureteralreflux still remains controversial.21,22 The sub-stance should be nontoxic, biocompatible, nonmi-gratory, nonantigenic, and cause minimal local in-flammation. To our knowledge, we report the firstprospective trial comparing two different bulkingagents with regard to efficacy and 1-year outcome. We limited our protocol to a single injection ofMacroplastique or Deflux, in contrast to previousstudies using multiple injections. This unique as-pect of a single injection allowed us to comparedifferent bulking agents in a much more standard-ized manner. Previous studies have indicated a
Difference in proportion of positive out-
success rate of 81% to 93% by endoscopic injection
comes. CI ϭ confidence interval.
using Macroplastique.23,24 The 86.2% success rate3 months after a single injection observed in our
ence (P ϭ 0.0536) was observed. No difference in
Macroplastique group confirmed this published
outcome according to gender was observed in ei-
data. In contrast to prior studies describing particle
ther group. Defining the success rate as no evi-
migration of less cross-linked silicone gels or non-
dence of reflux, the response rate after Macroplas-
cross-linked silicone oils with a particle diameter
tique and Deflux injection decreased to 75.8% and
of less than 100 m, Macroplastique is created as
62.5%, respectively. No significant dilation of the
an elastomer, minimizing the risk of migration.13,22
upper urinary tract was observed in either group.
Nonetheless, one has to take into consideration the
However, a temporary mild dilation of the collect-
possible risks of autoimmune reactions25 and ma-
ing system was found in 23 ureterorenal units
lignancy in the long term, which has been demon-
(40%) after Macroplastique injection and 12 (21%)
after Deflux injection. Contralateral de novo grade
In 1995, Stenberg and Lackgren15 introduced a
I reflux developed in 1 patient in both groups but
new bioimplant consisting of dextranomer micro-
did not require additional treatment. Neither ad-
spheres and hyaluronic acid (dextranomer/hyal-
verse reactions nor any signs of toxicity in either
uronic acid copolymer or Deflux). The short and
group were observed. Six and four patients had
long-term success rate of 68% to 75% in treating
postoperative afebrile urinary tract infection after
grade II or greater vesicoureteral reflux was re-
Macroplastique and Deflux injection, respectively.
ported after a single injection.27,28 The success rate
At 1 year of follow-up, 46 children (24 with 41
of 71.4% in our study was again consistent with the
ureters in the Macroplastique group, 22 with 32
published data. At 1 year of follow-up, reflux res-
ureters in the Deflux group) were available for re-
olution rates decreased gradually to 80.9% (Mac-
peated VCUG. Additional follow-up VCUGs of the
roplastique) and to 67.6% (Deflux). The trend to-
remaining patients were in progress at last follow-
ward higher success rates in the Macroplastique
up. The reflux resolution rate decreased gradually
group may be explained by the higher viscosity and
to 80.5% in the Macroplastique group and 68.8% in
absence of retraction of the substance. Because the
the Deflux group. On follow-up VCUG, initial
efficacy of Deflux compared with Macroplastique
grade III reflux in 2 patients (1 patient in either
showed no statistically significant differences with
group) had decreased to grade II reflux. Of a total
regard to reflux resolution, one can recommend
of 7 patients who had grade I reflux at 3 months of
the Deflux system as a reliable, new, alternative
follow-up (4 with 6 ureters in the Macroplastique
biodegradable bulking agent that permits defini-
group and 3 with 5 ureters in the Deflux group), 1
tive treatment in most children with vesicoureteral
patient with two ureterorenal units in the Macro-
reflux. Additionally, Deflux fulfills most of the cri-
plastique group and 2 patients with four uretero-
teria required for the ideal implantable bulking
renal units in the Deflux group developed grade II
agent and is advantageous over autologous agents
reflux after 12 months. No adverse reactions have
because it is inherently stable. Additionally, the
UROLOGY 60 (5), 2002
safety profile is highly satisfactory. Compared with
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UROLOGY 60 (5), 2002
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