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1.
Cardiol Young ; 32(8): 1289-1295, 2022 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-34666851

RESUMO

BACKGROUND: Truncus arteriosus is a rare CHD. Neonatal and early infancy repair is recommended though some cases may present late. The aim of our study is to investigate the current results of truncus arteriosus repair and to analyse the differences in outcome and reintervention need between early versus late truncus arteriosus surgical repair. MATERIAL AND METHODS: In this cohort study, we reviewed all children who underwent truncus arteriosus repair from 2001 till 2021. We divided patients into two groups; early repair group including patients repaired at age less than 3 months and late repair group including patients who had repair at 3 months of age and later. We compared both groups for outcome variables. RESULTS: Sixty-four children had truncus arteriosus repair including 48(75%) patients in early repair and 16(25%) patients in late repair groups. Peri-operative course was comparable between both groups. Post-surgery, we observed pulmonary hypertension in 6(12%) patients in early repair group comparing with 11(69%) patients in late repair group (p = 0.0001). In the last follow-up visit, pulmonary hypertension resolved in all early repair group patients while 6(37.5%) patients in late repair group continued to have pulmonary hypertension (p = 0.0001). Twenty-three(36%) patients required reintervention including 22(48%) in early repair group versus 1(6%) in late repair group (p = 0.007). CONCLUSION: In general, the outcome of early truncus arteriosus repair is excellent with resolution of pulmonary hypertension following early repair. Late repair caries higher risk of persistent pulmonary hypertension (37.5%). About one-third of the patients who had truncus arteriosus repair will require re-intervention within 38±38.4 months after initial surgery.


Assuntos
Hipertensão Pulmonar , Persistência do Tronco Arterial , Criança , Estudos de Coortes , Seguimentos , Cardiopatias Congênitas , Humanos , Hipertensão Pulmonar/cirurgia , Lactente , Recém-Nascido , Reoperação , Resultado do Tratamento , Tronco Arterial/cirurgia , Persistência do Tronco Arterial/cirurgia
2.
Childs Nerv Syst ; 37(2): 539-543, 2021 02.
Artigo em Inglês | MEDLINE | ID: mdl-32778939

RESUMO

PURPOSE: Myelomeningocele (MMC) is one of the commonest congenital malformations. Hydrocephalus develops in 65-85% of cases with MMC. Only 3-10% of MMC patients have normal urinary continence. We aim to investigate the effects of early and late operation in MMC patients in terms of development of hydrocephalus, motor deficits, and bladder functions. METHODS: Medical records of MMC patients operated between January 2008 and December 2014 were reviewed retrospectively. RESULTS: We retrospectively investigated patients' records of 43 patients. Twenty of the patients were operated within the first 48 h after the delivery (early repair group), while 23 of the patients were operated after 48 h of delivery (late repair group). In the early repair group, 15 patients were operated due to hydrocephalus. Urodynamic problems were detected in 17 (85%) patients. In the late repair group, shunts were placed in 14 (61%) patients during follow-up period and urodynamic problems were detected in 19 (82.6%) patients. Mean operation time for the late group was 4.6 months. There was no statistical difference between the early and late group in terms of neurological and urodynamic deficits. The mean follow-up period was 45.5 months. CONCLUSION: In the literature, surgery in the first 48 h of life is recommended for MMC patients. There was no difference between the early- and late-operated groups by means of hydrocephalus, urodynamic functions, and motor deficits in our study. Late surgery of intact sacs may avoid complications related to surgery in the neonatal period.


Assuntos
Hidrocefalia , Meningomielocele , Humanos , Hidrocefalia/etiologia , Hidrocefalia/cirurgia , Recém-Nascido , Meningomielocele/complicações , Meningomielocele/cirurgia , Duração da Cirurgia , Estudos Retrospectivos , Urodinâmica
3.
Pediatr Neurosurg ; 55(2): 106-112, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32454485

RESUMO

INTRODUCTION: Early repair in patients affected by myelomeningocele (MMC) is of paramount importance in order to prevent infection, minimize neural tissue damage, and reduce mortality. Treatment must include duraplasty and possibly an adequate soft tissue coverage. Delayed surgery in MMC patients can be more tedious due to the less clear borders between the placode and the skin. Moreover, the risks of wound infection and breakdown increase significantly. CASE PRESENTATION: We present the unusual case of a large MMC in a 3-year-old patient treated by combining the recently described cryopreserved amniotic membrane (AM) as homograft for dural reconstruction and a bilateral Keystone flap for soft tissue reconstruction. DISCUSSION: Thanks to its anti-inflammatory and elastic proprieties, the AM can play an important role in preventing adhesion between the reconstructed layers, thus reducing the risk of spinal cord tethering. The Keystone flap, at the same time, allows the wound tension to be distributed widely over the flap margins and not only along the midline, which overlies the duraplasty, enhancing the scar quality and lowering the risk of cerebrospinal fluid recurrence and wound dehiscence, with no donor site morbidity.


Assuntos
Aloenxertos/transplante , Âmnio/transplante , Criopreservação , Meningomielocele/cirurgia , Procedimentos de Cirurgia Plástica/métodos , Retalhos Cirúrgicos/transplante , Âmnio/fisiologia , Pré-Escolar , Feminino , Seguimentos , Humanos , Região Lombossacral/diagnóstico por imagem , Região Lombossacral/cirurgia , Meningomielocele/diagnóstico por imagem , Retalhos Cirúrgicos/fisiologia , Transplantes/fisiologia , Transplantes/transplante
4.
Pak J Med Sci ; 33(4): 984-987, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29067078

RESUMO

OBJECTIVE: To determine the early surgical outcomes of Tetralogy of Fallot (TOF) repair in children and young adults operated after the age of one year. METHODS: In this retrospective study, 307 cases of primary repair of Tetralogy of Fallot were done between September 2012 to February 2017, at CPE Institute of cardiology, Multan. Out of 307 operated patients, 4 (1.3%) patients had previous modified Blalock Taussig shunts, 2 (0.6%) associated ASD with TOF, 3 (0.9%) co-association of TOF with PDA, 2 (0.6%) had large conal arterial branch crossing the annulus, 3 (0.9%) had dextrocardia with situs inversus, 12 (3.9%) TOF with double outlet right ventricle (DORV), 2 (0.6%) were associated with complete AV canal defect, 8 (2.60%) with absent pulmonary valve syndrome, 15 (5.5%) with left pulmonary artery stenosis. Data of post-operative complications and operative parameters was recorded for all patients. RESULTS: Mean age of operated patients was 9.56±4.89 years. Post-operative complications occurred in 7.8% of patients. Most common post-operative complications were pleural effusion with a frequency of 12(3.9%) patients, and complete heart block in one patient. Insignificant small residual VSD was diagnosed in 8 (2.6%) patients. One moderately large VSD was closed surgically after one year of 1st surgery. Moderate to severe pulmonary valve regurgitation was diagnosed in 114 (37.1%) patients. Mild to moderate tricuspid regurgitation in 15 (4.8%) patients and moderate right ventricular outflow tract obstruction (RVOT) in 16 (5.2%) patients. Thirty-day mortality was only four (1.3%). CONCLUSION: Surgical correction of Tetralogy of Fallot (TOF) in children after one year carries good operative outcomes with minimum morbidity and mortality.

5.
World J Hepatol ; 14(2): 442-455, 2022 Feb 27.
Artigo em Inglês | MEDLINE | ID: mdl-35317176

RESUMO

BACKGROUND: The surgical management of bile duct injuries (BDIs) after laparoscopic cholecystectomy (LC) is challenging and the optimal timing of surgery remains unclear. The primary aim of this study was to systematically evaluate the evidence behind the timing of BDI repair after LC in the literature. AIM: To assess timing of surgical repair of BDI and postoperative complications. METHODS: The MEDLINE, EMBASE, and The Cochrane Library databases were systematically screened up to August 2021. Risk of bias was assessed via the Newcastle Ottawa scale. The primary outcomes of this review included the timing of BDI repair and postoperative complications. RESULTS: A total of 439 abstracts were screened, and 24 studies were included with 15609 patients included in this review. Of the 5229 BDIs reported, 4934 (94%) were classified as major injury. Timing of bile duct repair was immediate (14%, n = 705), early (28%, n = 1367), delayed (28%, n = 1367), or late (26%, n = 1286). Standardization of definition for timing of repair was remarkably poor among studies. Definitions for immediate repair ranged from < 24 h to 6 wk after LC while early repair ranged from < 24 h to 12 wk. Likewise, delayed (> 24 h to > 12 wk after LC) and late repair (> 6 wk after LC) showed a broad overlap. CONCLUSION: The lack of standardization among studies precludes any conclusive recommendation on optimal timing of BDI repair after LC. This finding indicates an urgent need for a standardized reporting system of BDI repair.

6.
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1559927

RESUMO

Introduction: Myelomeningocele is the most common form of spinal dysraphism. In the African context, late diagnosis and surgical treatment are frequent. Objective: To characterize an initial series of open myelomeningocele cases that received delayed repair at the Hôpital de Référence de Maradi. Methods: A series of five cases is presented, with open myelomeningocele, who received delayed surgical repair at the Hôpital de Référence de Maradi, Niger, between June - December 2022. The information was obtained from medical records and imaging records. Results: Five patients were intervened, three female and two male. In all cases the age of the patients at the time of surgery was greater than 30 days. All the dysraphisms were open, showing signs of partial or total epithelialization of the placode, at the time of the intervention. During the evaluation of neurological function, three of them exhibited distal paraplegia, with reflex and sphincter involvement. Laboratory tests showed, in all cases, hemoglobin levels below 12 mg/dl. None of the cases showed deterioration of the neurological state with respect to the preoperative evaluation. Conclusions: The surgical treatment of myelomeningocele in a low-resource setting, as is common in sub-Saharan Africa, has its own characteristics, marked by late presentation to specialized hospital centers, and the low nutritional status of patients. Surgical resection, partial or total, of an exposed and devitalized placode, with signs of epitalization, does not seem to influence the postoperative neurological status.


Introducción: El mielomeningocele es la forma más común de disrafismo espinal. En el contexto africano es frecuente su diagnóstico y tratamiento quirúrgico tardío. Objetivo: caracterizar una serie inicial de casos de mielomeningocele abiertos que recibieron reparación tardía en el Hôpital de Référence de Maradi. Métodos: Se presenta una serie de cinco casos, con MMC abiertos, quienes recibieron reparación quirúrgica tardía en el Hôpital de Référence de Maradi, Niger, entre junio - diciembre de 2022. La información se obtuvo de las historias clínicas y los registros imagenológicos. Resultados: Se intervinieron cinco pacientes, tres femeninos y dos masculinos. En todos los casos la edad de los pacientes al momento de la cirugía era mayor de 30 días. La totalidad de los disrafismos fueron abiertos, mostrando signos de epitelización parcial o total de la placoda, al momento de la intervención. Durante la evaluación de la función neurológica, tres de ellos exhibieron paraplejia distal, con afectación refleja y esfinteriana. Los exámenes de laboratorio mostraron, en todos los casos, niveles de hemoglobina inferiores a 12 mg/dl. Ninguno de los casos mostró deterioro del estado neurológico con respecto a la evaluación prequirúrgica. Conclusiones: El tratamiento quirúrgico del mielomeningocele en un entorno de bajos recursos, como es habitual en el África subsahariana, tiene características propias, marcadas por la presentación tardía a los centros hospitalarios especializados, y el bajo estado nutricional de los pacientes. La resección quirúrgica, parcial o total, de una placoda expuesta y desvitalizada, con signos de epitalización, no parece influir en el estado neurológico postoperatorio.

7.
Artigo em Inglês | MEDLINE | ID: mdl-26908387

RESUMO

Ventricular septal defect (VSD) is a rare complication of right ventricular infarction (RVI) which is associated with significant mortality, if not treated appropriately. It typically occurs within the first 10-14 days after myocardial infarction. Surgical repair has been shown to reduce in-hospital mortality from 90% to 33-45%. Early surgical VSD repair has also been associated with high 30-day operative mortality of 34-37%. Furthermore, after an acute MI the friable myocardium enhances the risk of recurrent VSD with early surgical repair. We present a case of a middle-aged woman who developed VSD after an RVI. Her surgical repair was delayed by 2 weeks due to development of Staphylococcus aureus bacteremia. During this period, she was managed medically and later on underwent percutaneous repair with an amplatzer VSD occluder device. Keeping this patient encounter in mind, we would like to emphasize on the limited recommendations available for early against late surgical repair of VSD.

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