PubMed Health⌕ Search

Biomedical subjects

J Wacksman

Publications and source records attributed to J Wacksman.

At least 37 records · Page 2Linked to original sources
PubMed1995

Evaluation of acute scrotum in the emergency department.

A 2-year retrospective review of 238 cases of acute scrotal pain encountered in a children's hospital emergency department is presented. The incidences of testicular torsion, torsion of a testicular appendage, and epididymitis were 16%, 46%, and 35%, respectively. Testicular salvage was critically dependent on the interval between onset of pain and surgical intervention. No testis likely to have been viable at the time of presentation was "lost." The diagnostic error rate on first encounter was 7%, resulting in 10 negative scrotal explorations. With the exception of cases of far-advanced necrotic testes, both color Doppler ultrasound and radioisotope imaging were highly specific diagnostic modalities. Thirty-nine percent of the children with epididymitis who underwent investigation were found to have either structural or functional urinary tract abnormalities. Noninvasive urodynamic studies appear to be useful screening modalities in older children with epididymitis.

Acute Disease↗
PubMed1995

Gastrocystoplasty: technical and metabolic characteristics of the most versatile childhood bladder augmentation modality.

The authors report on 23 patients who underwent complex continent urinary reconstructions, made successful by the selection of gastrocystoplasty as the chosen augmentation modality. The mean patient age was 6.1 years, and the mean weight was 17.9 kg. The minimum follow-up period was 1.5 years. The bladder capacity increased from a preoperative mean of 77.8 +/- 52.2 (SD) mL to a postoperative mean of 303.5 +/- 117.4 mL (P < .000001). No adverse effects on renal function or serum electrolyte composition were encountered, and there were no instances of acidosis or alkalosis. Continence was achieved in 91% of patients. In two patients (0.9%), hematuria-dysuria developed; one case was extremely mild. The other occurred only during a period of severe oliguria and resolved after transplantation. Gastrointestinal complications were minimal. Five patients had end-stage renal disease at the time of reconstruction and have since had successful transplantation. Gastrocystoplasty is particularly applicable to the pediatric population because of its unique anatomic and metabolic characteristics, which bestow tremendous versatility.

Acidosis↗
PubMed1995

Relative microbial resistance of gastric, ileal and cecal bladder augmentation in the rat.

PURPOSE: Bladder resistance to bacterial infection after gastrocystoplasty, ileocystoplasty and cecocystoplasty was investigated in the rat. MATERIALS AND METHODS: Bladders were infected with Escherichia coli 6 to 13 months after augmentation and urine culture was obtained weekly for 3 months. RESULTS: No differences were observed in the number of infected animals within each group or electrolyte data among groups. The number of animals infected after surgery but before E. coli challenge was lowest in the gastrocystoplasty group. Bladder stones formed only in ileocystoplasty and cecocystoplasty groups. No group had a change in urinary pH. CONCLUSIONS: Gastrocystoplasty may be associated with a lower incidence of spontaneous infection and stone formation. An aggressive infection protocol may have masked differences in susceptibility to infection. Since urinary pH was unchanged after gastrocystoplasty, use of the rat may not be appropriate for augmentation studies.

Animals↗
PubMed1995

Testicular autotransplantation: a 17-year review of an effective approach to the management of the intra-abdominal testis.

PURPOSE: Patients with intra-abdominal testes represent a small but challenging group who require innovative therapy. We report our 17-year experience with testicular autotransplantation. MATERIALS AND METHODS: Testicular autotransplantation was performed in 23 patients with 27 intra-abdominal testes. RESULTS: The success rate was 96% and average operative time was 4.25 hours with 40 to 90 minutes for vascular anastomoses. A contralateral Fowler-Stephens procedure had previously failed in 3 cases. CONCLUSIONS: Since the variability of collateral blood supply in patients with high undescended testes may potentially compromise the Fowler-Stephens procedure, we believe that testicular autotransplantation should be strongly considered in such patients, particularly those with bilateral undescended testicles.

Adolescent↗
PubMed1995

Epididymitis in older boys: dysfunctional voiding as an etiology.

Although male infants and young boys with epididymitis have a high incidence of anatomical pathology, dysfunctional voiding is not a well established cause of epididymitis. In our series 36 boys with epididymitis underwent noninvasive urodynamic studies to determine whether a physiological defect could be assigned as an etiology. The 2 mechanisms proposed are similar to that in children with vesicoureteral reflux associated with dyssynergia or bladder instability and to a cause of recurrent urinary tract infection in children (the infrequent voider syndrome). Urinalysis and urine culture are recommended in all children with epididymitis and urethral swabs are obtained from those who are sexually active. We recommend renal/bladder ultrasound and voiding cystourethrography in all infants and young children with epididymitis. In the older child we advocate detailed questioning regarding voiding symptoms and the performance of noninvasive urodynamic studies.

Adolescent↗
PubMed1994

Complete nonunion of the ureterovesical junction with preservation of renal function.

We report on a neonate with a history of failure to thrive who had a large right abdominal mass. Renal ultrasound showed a large cystic mass that arose from the upper pole of the hydronephrotic right kidney. Preoperative antegrade pyelography confirmed that the mass communicated with 1 kidney. Further evaluation revealed no communication of the ureter with the bladder or vagina. Exploratory surgery identified the mass and intraoperative pyelography revealed no communication with the bladder. After resection of the mass and nephrostomy placement, reimplantation of the right ureter demonstrated complete atresia of the distal right ureter. Preservation of the remaining renal parenchyma was possible, because the functioning lower pole collecting system communicated with the cystic mass that arose from the upper pole.

Female↗
PubMed1994

Laparoscopic correction of vesicoureteral reflux in the pig.

Extravesical detrusorrhaphy is a modification of the Lich-Gregoir antireflux procedure that incorporates ureteral advancement into the repair. We report on our use of laparoscopic detrusorrhaphy to correct vesicoureteral reflux in an animal model. Reflux was created by transurethral incision of the roof of each ureteral orifice. In phase 1 of this study, laparoscopic repair was performed 1 week later in 3 pigs and an open technique was done in the remainder. In phase 2 laparoscopic repair was done in 3 pigs 3 weeks after inducing vesicoureteral reflux. All phase 1 repairs successfully corrected reflux but 1 ureter in the laparoscopic group developed obstruction. All phase 2 repairs were successful, which was determined by preoperative and postoperative cystography, and a postoperative excretory urogram. Average time was 2 hours 21 minutes for laparoscopic repair and 1 hour 10 minutes for the open procedure. Complications included bladder perforation and ureteral obstruction in 1 case each with no postoperative deaths. These preliminary results indicate that laparoscopic detrusorrhaphy is a feasible procedure in a porcine model.

Animals↗
PubMed1993

Use of kidney internal splint/stent (KISS) catheter in urinary diversion after pyeloplasty.

We report on the use of a new catheter, the kidney internal splint/stent (KISS), to facilitate renal urine drainage following pyeloplasty. The catheter combines the desirable qualities of nephrostomy tube diversion, anastomotic stent, and trocar placement in a single tube. The special construction of its lumen diminishes the likelihood of obstructed drainage. Our experience using the KISS catheter with 31 patients undergoing pyeloplasty shows it provides effective internal and external urinary diversion.

Adolescent↗
PubMed1993

The modified pyramid hypospadias procedure: repair of megameatus and deep glanular groove variants.

We present our experience with the pyramid hypospadias repair in 37 patients with distal or subcoronal hypospadias. We also describe a significant modification (in the 7 most recent patients) of Duckett's original procedure that minimizes the risk of ventral fistula formation. This modification involves the creation of a vascularized second-layer tissue flap. We incorporated the modified pyramid hypospadias repair into the general surgical approach to subcoronal hypospadias. Our operative approach permits the delayed selection of either a perimeatal-based flap, preputial flap or a modified pyramid type repair after release of the shaft skin. In 35 patients the repair achieved excellent results, while only 2 had urethrocutaneous fistulas. No patient who underwent the modified repair suffered fistula formation. Our surgical technique is applicable to a number of variants of subcoronal hypospadias and maximizes repair options.

Humans↗
PubMed1993

Report of the Multicystic Kidney Registry: preliminary findings.

Multicystic kidney was first described in a 7-month-old child. Some physicians advocate nephrectomy in such cases, while others have questioned this procedure. In 1986 the American Academy of Pediatrics, Section on Urology established the Multicystic Kidney Registry to identify and follow patients with multicystic kidney disease. To date 441 patients have been registered, of whom 260 were managed nonoperatively. Based on followup of these patients no kidneys were removed for hypertension, infection, pain or tumor development. Long-term findings show that multicystic kidney disease may take as long as 20 years to resolve, and followup testing will be necessary.

Canada↗
PubMed1993

Multicystic dysplastic kidney in children: US follow-up.

Eighty-one cases of multicystic dysplastic kidney (MCDK) in children were diagnosed over the past 11 years at the authors' institution: 25 children had their kidneys surgically removed, eight with bilateral total involvement died, and 48 underwent serial follow-up ultrasonography (US) of their kidneys. Follow-up included 193 serial ultrasound (US) studies (mean, four per patient) for a total of 1,468 months (mean, 30.5 months). In the 48 patients followed up, 32 (67%) kidneys showed a decrease in size, nine (19%) showed no change, and five (10%) increased in size, and in two (4%), a change in size could not be determined. In seven of the 48 (15%) children, the MCDKs decreased in size, and, at follow-up US, no renal tissue could be found. In those patients in whom MCDKs decreased in size. Serial US characteristics changed from predominantly an enlarged cystic structure to a small dysplastic or absent kidney. Two of the five kidneys that increased in size were surgically removed, and MCDK was pathologically confirmed. A nonsurgical approach to the treatment of patients with MCDK is supported by this study.

Child, Preschool↗
PubMed1992

Results of the renewed extravesical reimplant for surgical correction of vesicoureteral reflux.

In 1987 Firlit et al described their results using Hodgson's technique of the modified extravesical Gregoir-Lich procedure. They coined the term detrusorrhaphy or extravesical ureteral advancement to describe this technique. During the last 4 years we performed this reimplantation on 211 ureters in 132 patients. Of the patients 79 had unilateral and 53 had bilateral procedures. Included were 6 megaureters requiring ureteral tailoring and 9 uncomplicated duplications. All but 1 patient were cured of reflux. No postoperative obstruction was encountered. Our results indicate that this is an excellent procedure to repair vesicoureteral reflux with minimal morbidity and short hospital stay.

Child↗
PubMed1992

Prenatal testicular torsion: principles of management.

To assess our experience with in utero testicular torsion, we retrospectively studied all newborns presenting in the newborn nursery with a diagnosis of neonatal testicular torsion. A total of 25 consecutive cases of torsion of the spermatic cord in 23 patients was identified and explored on an emergency basis. To our knowledge this represents the largest single institution series and 40% of all of the confirmed cases reported in the literature. No viable testicles were found. We strongly believe that torsion of the testis presenting at birth represents an irreversible intrauterine event best treated in an early elective setting. We suggest an inguinal approach with contralateral orchiopexy in all patients who present with signs and symptoms of prenatal (in utero) testicular torsion.

Female↗
PubMed1992

Distention of the posterior urethra: association with nonneurogenic neurogenic bladder (Hinman syndrome).

In nonneurogenic neurogenic bladder (NNNB), or Hinman syndrome, a functional bladder outlet obstruction is produced by voluntary contraction of the external sphincter during voiding. To determine whether any radiographic findings are diagnostic of this condition, the authors reviewed the genitourinary images of six boys in whom NNNB was diagnosed in the past 5 years. In contrast to true neurogenic bladder, findings of elongated, trabeculated, high-volume bladders with substantial postvoid residuals, obstructive uropathy, and vesicoureteral reflux were not associated with clinical, radiographic, or urodynamic evidence of an underlying neurologic abnormality. Furthermore, four boys had distention of the posterior urethra that the authors believe is suggestive of this condition. In these patients, the posterior urethra appeared entirely normal during early voiding, but distended after contraction of the external sphincter as voiding progressed. This posterior urethral distention may worsen the symptoms of enuresis, but may also reduce or retard the damage to the proximal urinary tract.

Child↗
PubMed1991

Occult neurovesical dysfunction in children with imperforate anus and its variants.

Neurovesical dysfunction (NVD) is frequently encountered in children with imperforate anus and its variants. Such functional urologic problems are often compounded by associated anatomic urologic abnormalities that in combination may profoundly alter the course and prognosis of children with imperforate anus. Herein, we report 16 such cases. Management of NVD in children with imperforate anus offers several unique challenges that require important alterations in management. Specific recommendation are presented.

Anus, Imperforate↗
PubMed1991

Elevated intravesical pressure causes arterial hypoperfusion in canine colocystoplasty: a fluorometric assessment.

Since 1988 there have been 15 reported cases of late, spontaneously ruptured intestinal cystoplasties at bowel sites remote from the anastomosis. Ischemic necrosis has been suggested as a possible etiology. We examined this hypothesis by quantifying the uptake of intravascular fluorescein in the augmented bowel of adult mongrel canines. There was a statistically significant decrease in fluorescein uptake at high intravesical pressures, which appeared to be most pronounced at the antimesenteric border. This laboratory study supports a recent clinical report of histological changes pathognomonic for chronic ischemia in the augmented bowel of patients with spontaneous rupture.

Anastomosis, Surgical↗
PubMed1991

Acquired structural genitourinary abnormalities contributing to deterioration of renal function in older patients with nephropathic cystinosis.

The natural progression of nephropathic cystinosis to end stage renal disease can be delayed, sometimes by many years, by the reducing agent, cysteamine, which lowers intracellular cystine content to near normal. We report on two patients with nephropathic cystinosis who were treated with cysteamine and developed structural genitourinary abnormalities which may have contributed to an increase in the rate of decline of renal function. One patient, aged 11 years, was found to have massive megacystis and hydroureteronephrosis but no anatomic bladder outlet obstruction. His abnormality was presumed to be related to chronic high urine volumes leading to megacystis and physiologic ureteral obstruction. Vesicostomy stabilized renal function. The second patient, aged 11 1/2 years, was found to have bilateral renal cystic disease which presumably was acquired and may have been related to long-standing hypokalemia. Minor renal abnormalities were found by ultrasound in five additional cystinotic children. We concluded that older children with nephropathic cystinosis may be prone to acquire structural abnormalities of their kidneys or urinary tract.

Creatinine↗