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The Journal of Urology | 2001

SIGMOID CYSTOPLASTY WITH ARGON BEAM WITHOUT MUCOSA

F. de Badiola; Eduardo Ruiz; J. C Puigdevall; Pablo Lobos; Juan Moldes; M. Lopez Raffo; A. Gallo

PURPOSE Intestinal bladder augmentations have well recognized complications, including mucus production, metabolic abnormalities and perforation. These complications may be avoided if the intestinal mucosa is not incorporated in the urinary tract. We report our experience with sigmoid cystoplasty without mucosa using argon beam, and describe the clinical, urodynamic, ultrasound and pathological results. MATERIALS AND METHODS We performed sigmoid cystoplasty without mucosa in 26 patients and with argon beam over the mucosa before it was removed in 6 boys and 4 girls with a mean age of 8 years (range 3 to 14). All patients had neurogenic bladder as the initial disease. Indications for augmentation were poor bladder compliance, low bladder capacity, hydronephrosis and urinary incontinence. Mean followup was 18 months (range 8 to 40) and included ultrasound, urodynamic evaluation, renal function and clinical assessment. In all patients intraoperative biopsies were done. In 8 of the 10 patients endoscopic biopsies of the augmented segment were obtained between 6 months and 2 years postoperatively. The operation consisted of the Goodwin technique without mucosa, which was treated with argon beam before it was removed. RESULTS The 10 patients are dry on intermittent clean catheterization with intervals of greater than 4 hours. There have been no clinical urinary tract infections. Two patients presented with peristaltic contractions and no symptoms. Bladder capacity increased from 80 (range 45 to 200) to 300 (220 to 400) ml., and mean postoperative compliance was 15 ml./cm. H2O (range 9 to 38). There were no significant changes in the urodynamic data between patients treated with sigmoid cystoplasty without mucosa only and with argon beam. Intraoperative biopsies after treatment with argon beam showed damaged mucosa and muscularis mucosa, and intact serosa, muscularis and submucosa layers. On the 8 argon beam postoperative biopsies the sigmoid submucosa was covered with a pseudostratified metaplasia of connective tissue with collagen fibers without scars (trichromic technique). CONCLUSIONS Sigmoid cystoplasty without mucosa with argon beam is easy to perform. The clinical and urodynamic results have been satisfactory, and use of argon beam prevents postoperative bleeding and residual glands.


Journal of Pediatric Urology | 2006

Kidney transplantation in small children with live related donors: 20 years of experience

Eduardo Ruiz; Javier Escalante Cateriano; Pablo Lobos; Francisco de Badiola; Marcelo Boer; Juan Moldes; J. C Puigdevall; Jorge Ferraris

OBJECTIVES Kidney transplantation (Tx) with a live related donor is the best option available for the treatment of end-stage renal disease at any age. Modern dialysis has allowed many very young and small children to receive a renal transplant with good results in spite of the limitations of space and the size of the adult kidney. Here, we report our experience with renal Tx with live related donors in this complex group of pediatric patients. MATERIAL AND METHODS From 1978 to 2004 a kidney transplantation was performed in 211 pediatric patients. Of this group, 23 patients between 1 and 10 years of age (16 males and seven females) of less than 17 kg (8.9-16.9 kg) received their first live related donor transplantation between 1985 and 2004. Renal insufficiency was secondary to nephropathy in 11 patients, infravesical obstruction in six and renal dysplasia or renal infarcts in six. RESULTS Patient and graft survival was 100% and 95.6% with an average follow up of 89.6 months (6-231). There were no vascular or urological complications. Urinary infection in five (21.7%) and acute rejection in three (13%) were the most common complications. One patient has returned to dialysis 11 years after Tx. CONCLUSIONS Young pediatric patients with a low body weight did not suffer a higher percentage of postoperative surgical complications, and the follow-up results are similar to those in older patients. A complex urological malformation has not prevented a living related Tx. These results encourage us to perform this procedure more frequently in younger patients when a live donor is available.


Pediatric Critical Care Medicine | 2007

Internal mammary artery injury after central venous catheterization.

Pablo G. Eulmesekian; Augusto Pérez; Pablo Minces; Pablo Lobos; Juan Moldes; Ricardo García Mónaco

Objective: We describe an infrequent but potentially lethal complication: an iatrogenic injury of the internal mammary artery after central venous catheterization. Design: Report of cases. Setting: Pediatric intensive care unit. Patients: The first patient we report on is a 3-yr-old girl who was severely neurologically damaged and was admitted to the pediatric intensive care unit for aspiration pneumonia and septic shock. Immediately after vein cannulation on the left internal jugular vein, the patient suffered hypotension and cardiac arrest, secondary to an adequately drained massive hemothorax. Restoration of spontaneous circulation was initially achieved, and the patient was transferred to the angiographic suite. Selective angiography during cardiopulmonary resuscitation for a second cardiac arrest revealed a laceration of the internal mammary artery. Resuscitation was not successful, and the patient died. The second case reported is a 7-yr-old girl admitted for bone marrow transplantation. She was electively taken to the angiographic suite for central venous insertion. An infraclavicular approach of the right subclavian vein was attempted, but radioscopy showed the guidewire inside the pleural space. Soon thereafter, the patient became hypotensive and was in shock. Radioscopy showed a large pleural effusion and a massive hemothorax was drained. Selective angiography demonstrated an injured internal mammary artery was embolized. Hemodynamics improved, and the patient was transferred to the pediatric intensive care unit, where she was extubated 12 hrs later. Interventions: None. Conclusions: Central venous catheter placement in the intrathoracic vein may cause potentially lethal complications in the form of an injury to the internal mammary artery. Hypotension during or immediately after the procedure should be a warning of a serious adverse event, such as massive hemothorax, that may compromise life. Adequate drainage of the pleural cavity may not completely relieve vascular compression if some of the bleeding from an injured internal mammary artery is extrapleural. Early diagnosis and treatment by selective embolization of the injured vessel in interventional radiology is the first therapeutic choice and may be life saving.


The Journal of Urology | 2006

14 years of experience with the artificial urinary sphincter in children and adolescents without spina bifida

Eduardo Ruiz; J. C Puigdevall; Juan Moldes; Pablo Lobos; Marcelo Boer; J. Ithurralde; J. Escalante; F. de Badiola


Acta gastroenterologica Latinoamericana | 2011

Choledochal cyst in pediatric patients: a 10 years single institution experience

Micaela Germani; Daniel Liberto; Gastón Elmo; Pablo Lobos; Eduardo Ruiz


Archivos Argentinos De Pediatria | 2005

Manejo interdisciplinario de un quilotórax congénito complicado con hidropesía fetal

Diego Elias; Horacio Aiello; Gustavo Izbizky; Marina Ferreira; Pablo Lobos; Carlos Fustiñana; Eduardo Ruiz; Lucas Otaño


Medicina-buenos Aires | 2015

Metástasis pulmonares en osteosarcoma neoadyuvancia, tratamiento quirúrgico y supervivencia

German L. Farfalli; Pablo Lobos; David Smith; Patricia Streitenberger; María P Rodríguez; Luis A. Aponte-Tinao


Archivos Argentinos De Pediatria | 2013

Enfermedad de Castleman de localización cervical: Caso clínico pediátrico

Julia Udaquiola; Daniel Liberto; Tamara Kreindel; Hernán García Rivello; Pablo Lobos


Archivos Argentinos De Pediatria | 2014

Síndrome aspirativo por hendidura laríngea en un lactante

Giselle Cuestas; Victoria Demarchi; Adrián Zanetta; Mauricio Urquizo; Pablo Lobos; Juan Razetti


Archivos Argentinos De Pediatria | 2013

Tratamiento de las estenosis laríngeas adquiridas en pediatría: Serie de casos

Giselle Cuestas; Mauricio Urquizo; Victoria Demarchi; Adrián Zanetta; Pablo Lobos; Juan Razetti

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Juan Moldes

Hospital Italiano de Buenos Aires

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J. C Puigdevall

Hospital Italiano de Buenos Aires

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Daniel Liberto

Hospital Italiano de Buenos Aires

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Adrián Zanetta

Hospital Italiano de Buenos Aires

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Ana Morandi

Hospital Italiano de Buenos Aires

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F. de Badiola

Hospital Italiano de Buenos Aires

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Francisco Debadiola

Hospital Italiano de Buenos Aires

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Gastón Elmo

Hospital Italiano de Buenos Aires

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