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1.
Dis Esophagus ; 32(6)2019 Jun 01.
Article de Anglais | MEDLINE | ID: mdl-30828713

RÉSUMÉ

The aim of this study is to investigate management and outcome in esophageal atresia (EA) and to identify early predictive factors of morbidity and mortality in a developing country. Charts of neonates with repaired EA from 2007 to 2016 were reviewed. Patients' characteristics, operative details, and postoperative outcomes were collected. Statistical analyses were performed to identify predictors of complicated evolution. Forty-two cases were collected. There were 14 girls and 28 boys. Only one patient had antenatal diagnosis (2.3%). The mean gestational age was 38 weeks. Nine patients (21.4%) weighed less than 2.5 kg. Seventeen (40.4%) patients had associated malformations most commonly cardiac (9/17). Thirteen patients had delayed diagnosis (30.9%). Thirty-nine (92.8%) patients underwent primary esophageal anastomosis. Overall survival was 76.2%. Nineteen patients (57% of survivals) had complicated evolution before the age of one year and 15 patients (46.8% of survivals) developed complications after the age of one year. Perinatal variables associated with mortality were prematurity (p = 0.004, OR = 5.4, IC95% = [1.13-25.80]), low birth weight (p = 0.023, OR = 7, IC95% = [1.38-35.47]), cardiac malformations (p = 0.006, OR = 10.5, IC95% = [2.03-54.27]) and delayed diagnosis (p = 0.005, OR = 10.11, IC95% = [2.005-50.980]). Variables associated with short-term and middle-term complications were duration of intubation (p = 0.019, OR = 0.118, IC95% = [0.019-0.713]) and the presence of short-term complications (p = 0.016, OR = 7.33, IC95% = [1.467-36.664]) respectively. These factors may be used to identify patients who will benefit from more intensive follow-up program.


Sujet(s)
Pays en voie de développement/statistiques et données numériques , Atrésie de l'oesophage/mortalité , Atrésie de l'oesophage/chirurgie , Fistule oesophagienne/étiologie , Oesophage/chirurgie , Anastomose chirurgicale/effets indésirables , Désunion anastomotique/étiologie , Atrésie de l'oesophage/diagnostic , Sténose de l'oesophage/étiologie , Femelle , Humains , Nourrisson , Nouveau-né , Intubation trachéale/effets indésirables , Mâle , Études rétrospectives , Facteurs de risque , Taux de survie , Tunisie/épidémiologie
6.
Prog Urol ; 27(2): 87-92, 2017 Feb.
Article de Anglais | MEDLINE | ID: mdl-28117236

RÉSUMÉ

BACKGROUND AND OBJECTIVE: Mini-invasive surgery is still evolving to get better surgical conditions for patients with ureteropelvic junction obstruction. We used technical modifications (hybrid pyeloplasty) that simplify surgical steps of laparoendoscopic single-site pyeloplasty in children. Our aim was to compare hybrid pyeloplasty to laparoendoscopic single-site pyeloplasty and to open pyeloplasty. PATIENTS AND METHODS: We retrospectively reviewed records of patients with ureteropelvic junction obstruction aged<14years undergoing pyeloplasty at our institute from January 2011 to December 2015. Demographic data, laterality, operative time, length of hospital stay, drainage tubes, and postoperative complications were recorded. Surgical outcomes were evaluated based on renal sonography and Lasix diuretic renography. RESULTS: Among 38 patients, 17 underwent open pyeloplasty (group I), 10 had laparoendoscopic single-site pyeloplasty (group II) and 11 had hybrid pyeloplasty (group III). The mean age at the time of operation was 55 months. The operative time in group III was significantly shorter than that in group I and group II (P<0.001). The shortest median hospital stay was noted in the group III. The mean follow-up period was 26 months (range: 6-52 months). CONCLUSION: The hybrid pyeloplasty using LESS combine the successful outcomes of open surgery and advantages of minimally invasive surgery. It offers small incision surgery, good working space, short operation time, secure anastomosis and good cosmetic results. LEVEL OF EVIDENCE: 5.


Sujet(s)
Pelvis rénal/chirurgie , Laparoscopie , Uretère/chirurgie , Obstruction urétérale/chirurgie , Urétéroscopie , Enfant , Enfant d'âge préscolaire , Femelle , Humains , Mâle , Études rétrospectives
7.
Prog Urol ; 25(10): 598-602, 2015 Sep.
Article de Français | MEDLINE | ID: mdl-26094098

RÉSUMÉ

INTRODUCTION: The single scrotal incision orchidopexy was described by Bianchi in 1989. Despite its popularity, the place of this technique in the treatment of cryptorchidism in children is still unclear. AIM OF THE STUDY: To evaluate and compare the outcomes of the conventional inguinal approach and the scrotal approach for the treatment of palpable undescended testis in children. METHODS: A prospective study for all patients with palpable undescended testis undergoing orchidopexy between January 2011 and December 2013 was conducted. Totally 200 patients were randomly divided into two groups: group 1: two incisions inguinal approach (80 patients, 100 testis); group 2: single scrotal incision approach (89 patients, 100 testis). MAIN RESULTS: The patients' mean age was 53.9±13 months in group 1 and 45.8±9 months in group 2. There was no statistical difference between the two groups in terms of patient age (P=0.8) and location of the undescended testis (P=0.359). Operative time was statistically significantly lower in the scrotal group (P<0.05). There was a significant difference in the complications rates between the two groups. CONCLUSION: The single scrotal incision orchidopexy is safe and effective for undescended testicles palpable in the inguinal canal or in high scrotal position.


Sujet(s)
Cryptorchidie/chirurgie , Canal inguinal/chirurgie , Orchidopexie/méthodes , Scrotum/chirurgie , Enfant , Enfant d'âge préscolaire , Humains , Nourrisson , Nouveau-né , Mâle , Durée opératoire , Complications postopératoires , Études prospectives
8.
Arch Pediatr ; 22(5): 533-5, 2015 May.
Article de Anglais | MEDLINE | ID: mdl-25819593

RÉSUMÉ

Ovarian transposition was the first procedure proposed for children with cancer to preserve ovarian function from damage caused by abdominal and pelvic radiotherapy. In this paper, we describe the first pediatric case of single-port laparoscopic ovarian transposition.


Sujet(s)
Maladie de Hodgkin/thérapie , Laparoscopie/méthodes , Interventions chirurgicales mini-invasives/méthodes , Ovaire/effets des radiations , Ovaire/transplantation , Lésions radiques/prévention et contrôle , Radiothérapie adjuvante/effets indésirables , Transplantation hétérotopique/méthodes , Enfant , Association thérapeutique , Femelle , Maladie de Hodgkin/anatomopathologie , Humains , Stadification tumorale
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