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606 International Abstracts of Pediatric Surgery
was Wilms' tumor 56 (19%), non–Hodgkin lymphoma 71 (24%),
Hodgkin's lymphoma 64 (22%), rhabdomyosarcoma 32 (11%) and
neuroblastoma 68 (24%). There were a total of 12 bowel obstructions in
11 patients (3.7%). Mean follow-up was 3.6 ± 2.7 years. Children with
SBO were more likely to be male (4.5 : 1, P0.061) and younger (4.2 years
vs. 8.1yrs; P 0.087), Wilms' tumor accounted for 45% of patients with
SBO, but made up only 19% of the study population. The incidence of
SBO in patients with Wilms' tumor was 8.9% compared to 3.8% overall
incidence (P 0.043).
It is concluded that SBO is relatively uncommon after intra-abdominal
malignancies. Wilms' tumor, Burkitt's lymphoma, and rhabdomyosarcoma
appear to be associated with the highest risk of SBO.—
Thomas A. Angerpointner
doi:10.1016/j.jpedsurg.2010.11.054
Transanal endorectal vs. Duhamel pull-through forHirachsprung's diseaseGunnarsdottir A, Larsson L-T, Ambjörnsson E. Eur J Pediatr Surg 2010
(August);20/4:242-6
The aim of this study was to test the hypothesis that the early functional
outcome for patients with rectosigmoid Hirschsprung' s disease (HD) is
comparable for the Duhamel pull-through procedure and the transanal pull-
through (TERPT) procedure, with less discomfort for the patient
postoperatively after the TERPT technique. Eleven patients operated on
with the TERPT technique (T-group) were prospectively registered and
compared retrospectively with 18 patients operated on with the Duhamel
pull-through (D-group). Data recorded included patient demographics,
operative treatment, complications, hospital stay and bowel functions.
Follow-up time was limited to 24 months.
The T-group started oral feeding sooner, their bowel movement started
sooner, they had less need for analgesics postoperatively and a significantly
shorter hospital stay. Seventy one percent of the patients in the D-group
needed re-intervention as compared to only 18% of the T-group.
Enterocolitis was seen in two patients in both groups. At the last clinical
control ten patients had constipation (59%) and three had soiling (18%) in the
D-group. Three patients in the T-group had constipation (27%) and one had
soiling (9%).
In conclusion, the results support the use of the TERPT method rather than
the Duhamel pull-through for rectosigmoid HD.—
Thomas A. Angerpointner
doi:10.1016/j.jpedsurg.2010.11.055
Laparoscopic mesh rectopexy for complete rectal prolapse in children:a new simplified techniqueShalaby R, Ismail M, Abdelaziz M. Pediatr Surg Int 2010;26:807-13
Rectal prolapse in children without underlying conditions is usually a self-
limiting problem and requires no surgical treatment. For children with
persistent rectal prolapse, a variety of surgical procedures have been
described. This paper presents a novel simplified laparoscopic technique for
management of those patients. The aim of this study is to evaluate the results
that can be achieved by using this technique in management of persistent
complete rectal prolapse in children.
The authors reviewed the reports of 680 patients with primary complete and
partial rectal prolapse over the period from August 2000 to August 2008.
Fifty-two patients with complete primary rectal prolapse refractory to
medical treatment for 2 years underwent a novel simplified technique for
laparoscopic mesh rectopexy. The technique involves laparoscopic posterior
rectal mobilization, retroperitoneal presacral mesh placement, and fixation
of the redundant sigmoid to the mesh.
Nonoperative management was successful with no recurrences in 628
patients (92.4%), whereas 52 (7.6%) patients did not respond to non-
operative management at a median follow-up period of 2 years. They
were 35 males and 17 females. Their ages ranged from 2 to 14 years
(mean 6). All patients were successfully subjected to laparoscopic mesh
rectopexy without any conversion. The mean duration of surgery was
40 min. No intraoperative complications were reported, but one patient
developed postoperative constipation that responded well to conservative
treatment. The mean postoperative hospitalization was 2 days. Two cases
were lost to follow-up, while the others were available for 36 months.
There was no recurrence. The authors conclude that laparoscopic mesh
rectopexy is a safe, rapid, effective technique. It improved functional
outcome without recurrence. It is associated with minimal postoperative
pain and short hospital stay with excellent cosmetic result.—
Federico G. Seifarth
doi:10.1016/j.jpedsurg.2010.11.056
The efficacy of external neuromyogenic stimulation on neuromuscularanorectal incontinenceErgun O, Tatlisu R, Pehlivan M, et al. Ezr J Pediatr Surg 2010 (August);
20/4:230-3
This study presents the preliminary results of external neuromyogenic
electrostimulation (EMS) for the treatment of anorectal continence problems.
A total of 17 patients with anorectal malformations (n = 11), Hirsch-
sprung's disease (n = 5) or pelvi-perineal trauma (n = 1) were included in
the study. All patients were evaluated using clinical, radiological and
manometric methods prior to ENS. The Holschneider Continence Scale and
the Quality of Life (QOL) score were used for clinical assessment. The
ENS stimulator is a two channel ambulatory device providing a pulse
current. ENS was performed by parents in a home setting twice daily, using
a skin electrodes attached to the sides of the anus. ENS was continued for
6 weeks. Clinical and manometric variables were reevaluated following the
6-week program.
Mean age of the patients was 9.7 years (range 5-22 years) . The
Holschneider Continence Score increased from a mean value of 5.3 ± 3.2
to 12.4 ± 1.7 significantly (P = .002) and mean QOL stores from 5.6 ± 2.3
to 11.6 ± 1.8 (P = .01) following ENS. Mean anal resting pressures
prior to ENS were 20.3 ± 6 cm H2 and increased to 28.7 ± 14.7 cm H2
after 6 weeks (P = .05). Maximum voluntary squeeze pressures before an
after ENS were 56.1 ± 16.7 cm H2 and 100.7 ± 16.9 cm H2O, respectively
(P = .001). Preliminary results of ENS thus have shown that patients
achieved higher maximum voluntary squeeze pressures, and showed a
marked improvement in their continence and QOL scores. Given the
advantage of ambulatory use in a home setting, the ENS seems promising
in terms of achieving improved anorectal continence in selected
patients.—Thomas A. Angerpointner
doi:10.1016/j.jpedsurg.2010.11.057