The Experts below are selected from a list of 360 Experts worldwide ranked by ideXlab platform
Groenen M.j. - One of the best experts on this subject based on the ideXlab platform.
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[The Ogilvie Syndrome in elderly patients with multimorbidity]
'Springer Science and Business Media LLC', 2014Co-Authors: Tan A.c., Olde Rikkert M.g.m., Groenen M.j.Abstract:Two patients presented with the Ogilvie Syndrome which is an acute colonic pseudo-obstruction without any mechanical obstruction. Both patients suffered from multiple medical conditions such as infections, electrolyte disturbances and functional decline.The Ogilvie Syndrome is particularly seen in patients with multimorbidity who stay in the hospital or nursing home. The incidence of the Ogilvie Syndrome will probably increase because of ageing of our population and will be most prevalent in the frail elderly. The precise mechanism of this disease is still unclear, but there is evidence in the literature that the aetiology is multifactorial and runs via autonomic dysregulation of the colon.Early recognition and appropriate treatment may reduce the risk of complications and limit mortality, also depending on the related comorbidity
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[The Ogilvie Syndrome in elderly patients with multimorbidity]
'Springer Science and Business Media LLC', 2014Co-Authors: Tan A.c., Olde Rikkert M.g.m., Groenen M.j.Abstract:Item does not contain fulltextTwo patients presented with the Ogilvie Syndrome which is an acute colonic pseudo-obstruction without any mechanical obstruction. Both patients suffered from multiple medical conditions such as infections, electrolyte disturbances and functional decline.The Ogilvie Syndrome is particularly seen in patients with multimorbidity who stay in the hospital or nursing home. The incidence of the Ogilvie Syndrome will probably increase because of ageing of our population and will be most prevalent in the frail elderly. The precise mechanism of this disease is still unclear, but there is evidence in the literature that the aetiology is multifactorial and runs via autonomic dysregulation of the colon.Early recognition and appropriate treatment may reduce the risk of complications and limit mortality, also depending on the related comorbidity
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Het Ogilvie-syndroom bij oudere patienten met multiproblematiek
'Springer Science and Business Media LLC', 2014Co-Authors: Tan A.c., Olde Rikkert M.g.m., Groenen M.j.Abstract:Item does not contain fulltextTHE Ogilvie Syndrome IN ELDERLY PATIENTS WITH MULTIMORBIDITY: Two patients presented with the Ogilvie Syndrome which is an acute colonic pseudo-obstruction without any mechanical obstruction. Both patients suffered from multiple medical conditions such as infections, electrolyte disturbances and functional decline.The Ogilvie Syndrome is particularly seen in patients with multimorbidity who stay in the hospital or nursing home. The incidence of the Ogilvie Syndrome will probably increase because of ageing of our population and will be most prevalent in the frail elderly. The precise mechanism of this disease is still unclear, but there is evidence in the literature that the aetiology is multifactorial and runs via autonomic dysregulation of the colon.Early recognition and appropriate treatment may reduce the risk of complications and limit mortality, also depending on the related comorbidity
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Het Ogilvie-syndroom bij oudere patienten met multiproblematiek
'Springer Science and Business Media LLC', 2014Co-Authors: Tan A.c., Olde Rikkert M.g.m., Groenen M.j.Abstract:THE Ogilvie Syndrome IN ELDERLY PATIENTS WITH MULTIMORBIDITY: Two patients presented with the Ogilvie Syndrome which is an acute colonic pseudo-obstruction without any mechanical obstruction. Both patients suffered from multiple medical conditions such as infections, electrolyte disturbances and functional decline.The Ogilvie Syndrome is particularly seen in patients with multimorbidity who stay in the hospital or nursing home. The incidence of the Ogilvie Syndrome will probably increase because of ageing of our population and will be most prevalent in the frail elderly. The precise mechanism of this disease is still unclear, but there is evidence in the literature that the aetiology is multifactorial and runs via autonomic dysregulation of the colon.Early recognition and appropriate treatment may reduce the risk of complications and limit mortality, also depending on the related comorbidity
Alejandro Valdes Cepeda - One of the best experts on this subject based on the ideXlab platform.
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acute colonic pseudo obstruction Ogilvie Syndrome post renal transplantation
Boletín médico del Hospital Infantil de México, 2016Co-Authors: Erik Antonio Mier Escurra, Sergio Javier Fernández Ortíz, Talia Diaz Prieto, Guillermo Mier Saad, Alejandro Valdes CepedaAbstract:Abstract Background Acute colonic pseudo-obstruction, also known as Ogilvie Syndrome, is a rare gastrointestinal Syndrome in children. It is characterized by a marked dilatation of the colon evidenced by imaging and absence of mechanical obstruction. Patients typically present abdominal pain and distention, tympanic abdomen with peristalsis accompanied by nausea and vomiting. Up to 40% of patients can pass gas and have bowel movements. This Syndrome is very rare in pediatric patients, and no cases have been reported in a post-renal transplant pediatric patient. Case report A 13-year-old male patient with a medical history of psychomotor retardation due to perinatal asphyxia and chronic renal failure secondary to bilateral renal hypoplasia was treated with peritoneal dialysis for one year until kidney transplantation. Currently, he is under immunosuppressive regimen. His condition began with mild abdominal pain accompanied by semi-liquid stools, and progressive distention up to 78 cm of abdominal circumference in 72 hours. Image studies were performed. Managed with prokinetic drugs without any improvement. Two exploratory laparotomies observed flanges, without evidence of any mechanical obstruction. An abdominal magnetic resonance was performed, where important intestinal dilatation was observed and no evidence of mechanical obstruction. Ogilvie's Syndrome was diagnosed, and management with neostigmine was initiated, which led to symptom resolution. Conclusions This Syndrome is very rare in children. Therefore, there is little clinical suspicion and lack of management guidelines for diagnosis and treatment of patients of this age.
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Acute colonic pseudo-obstruction (Ogilvie Syndrome) post-renal transplant [Pseudo-obstrucción colónica aguda (síndrome de Ogilvie) post-trasplante renal]
'Elsevier BV', 2016Co-Authors: Sergio Javier Fernández Ortíz, Alejandro Valdes CepedaAbstract:Background Acute colonic pseudo-obstruction, also known as Ogilvie Syndrome, is a rare gastrointestinal Syndrome in children. It is characterized by a marked dilatation of the colon evidenced by imaging and absence of mechanical obstruction. Patients typically present with abdominal pain and distended, tympanic abdomen, with peristalsis present, accompanied by nausea and vomiting. Up to 40% of patients can pass gas and/or have bowel movements. We decide to report this case because this Syndrome is very rare in pediatric patients, and no cases have been reported in a post-renal transplant pediatric patient. Case report 13 year old male patient with past medical history of psychomotor retardation due to perinatal asphyxia and chronic renal failure secondary to bilateral renal hypoplasia. Treated with peritoneal dialysis for one year until kidney transplant was performed. Currently under immunosuppressive regime. He began his condition with mild abdominal pain accompanied by semi-liquid stools, and progressive distention up to 78\ua0cm of abdominal circumference in 72\ua0hours, so image studies were performed. Managed with prokinetic drugs without any improvement. Two exploratory laparotomies observed flanges, without evidence of any mechanical obstruction. An abdominal magnetic resonance was performed, where important intestinal dilatation was observed with no evidence of mechanical obstruction. Ogilvie Syndrome was diagnosed, so management with neostigmine was established, which led to symptom resolution. Conclusions This case is reported because this Syndrome is very rare in children, there is little clinical suspicion and lack of management guides for diagnosis and treatment in patients of this age. © 2016 Hospital Infantil de México Federico Góme
Valdes Cepeda Alejandro - One of the best experts on this subject based on the ideXlab platform.
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Pseudo-obstrucción colónica aguda (síndrome de Ogilvie) post-trasplante renal
Hospital Infantil de México Federico Gómez. Published by Masson Doyma México S.A., 2016Co-Authors: Mier Escurra, Erik Antonio, Díaz Prieto Talia, Fernández Ortíz, Sergio Javier, Mier Saad Guillermo, Valdes Cepeda AlejandroAbstract:ResumenIntroducciónLa pseudo-obstrucción colónica aguda, conocida también como síndrome de Ogilvie, es una condición gastrointestinal poco frecuente en pediatría. Se caracteriza por una marcada dilatación del colon en estudios de imagen y ausencia de obstrucción mecánica. Los pacientes se presentan clásicamente con dolor abdominal y abdomen distendido, timpánico con peristalsis presente, acompañado de náusea y vómito. Hasta el 40% de los pacientes canalizan gases o evacúan. Este caso se reporta debido a lo raro que es este síndrome en pacientes infantiles y a que no hay casos reportados en un paciente pediátrico post-trasplante renal.Caso clínicoPaciente masculino de 13 años de edad con antecedente de retraso psicomotor posterior a asfixia perinatal e insuficiencia renal crónica secundaria a hipoplasia renal bilateral. Fue tratado mediante diálisis peritoneal durante un año hasta la realización del trasplante renal. Se encuentra en manejo con inmunosupresores. Inició su padecimiento actual al presentar dolor abdominal leve acompañado de evacuaciones semilíquidas, posteriormente presentó distensión abdominal progresiva de hasta 78cm de perímetro abdominal, por lo que se realizaron estudios de imagen. Se prescribieron medicamentos procinéticos, sin mejoría. Se realizaron 2 laparotomías exploratorias observándose bridas, sin datos de obstrucción mecánica. Se realizó una resonancia magnética abdominal, observándose importante dilatación intestinal sin datos de obstrucción mecánica. Se diagnosticó síndrome Ogilvie y se administró neostigmina, presentando resolución del cuadro clínico.ConclusionesSe reporta este caso debido a que es un síndrome muy raro en la edad pediátrica, existe poca sospecha clínica y hacen falta guías de manejo para el diagnóstico y tratamiento en pacientes infantiles.AbstractBackgroundAcute colonic pseudo-obstruction, also known as Ogilvie Syndrome, is a rare gastrointestinal Syndrome in children. It is characterized by a marked dilatation of the colon evidenced by imaging and absence of mechanical obstruction. Patients typically present with abdominal pain and distended, tympanic abdomen, with peristalsis present, accompanied by nausea and vomiting. Up to 40% of patients can pass gas and/or have bowel movements. We decide to report this case because this Syndrome is very rare in pediatric patients, and no cases have been reported in a post-renal transplant pediatric patient.Case report13 year old male patient with past medical history of psychomotor retardation due to perinatal asphyxia and chronic renal failure secondary to bilateral renal hypoplasia. Treated with peritoneal dialysis for one year until kidney transplant was performed. Currently under immunosuppressive regime. He began his condition with mild abdominal pain accompanied by semi-liquid stools, and progressive distention up to 78cm of abdominal circumference in 72hours, so image studies were performed. Managed with prokinetic drugs without any improvement. Two exploratory laparotomies observed flanges, without evidence of any mechanical obstruction. An abdominal magnetic resonance was performed, where important intestinal dilatation was observed with no evidence of mechanical obstruction. Ogilvie Syndrome was diagnosed, so management with neostigmine was established, which led to symptom resolution.ConclusionsThis case is reported because this Syndrome is very rare in children, there is little clinical suspicion and lack of management guides for diagnosis and treatment in patients of this age
Tan A.c. - One of the best experts on this subject based on the ideXlab platform.
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[The Ogilvie Syndrome in elderly patients with multimorbidity]
'Springer Science and Business Media LLC', 2014Co-Authors: Tan A.c., Olde Rikkert M.g.m., Groenen M.j.Abstract:Two patients presented with the Ogilvie Syndrome which is an acute colonic pseudo-obstruction without any mechanical obstruction. Both patients suffered from multiple medical conditions such as infections, electrolyte disturbances and functional decline.The Ogilvie Syndrome is particularly seen in patients with multimorbidity who stay in the hospital or nursing home. The incidence of the Ogilvie Syndrome will probably increase because of ageing of our population and will be most prevalent in the frail elderly. The precise mechanism of this disease is still unclear, but there is evidence in the literature that the aetiology is multifactorial and runs via autonomic dysregulation of the colon.Early recognition and appropriate treatment may reduce the risk of complications and limit mortality, also depending on the related comorbidity
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[The Ogilvie Syndrome in elderly patients with multimorbidity]
'Springer Science and Business Media LLC', 2014Co-Authors: Tan A.c., Olde Rikkert M.g.m., Groenen M.j.Abstract:Item does not contain fulltextTwo patients presented with the Ogilvie Syndrome which is an acute colonic pseudo-obstruction without any mechanical obstruction. Both patients suffered from multiple medical conditions such as infections, electrolyte disturbances and functional decline.The Ogilvie Syndrome is particularly seen in patients with multimorbidity who stay in the hospital or nursing home. The incidence of the Ogilvie Syndrome will probably increase because of ageing of our population and will be most prevalent in the frail elderly. The precise mechanism of this disease is still unclear, but there is evidence in the literature that the aetiology is multifactorial and runs via autonomic dysregulation of the colon.Early recognition and appropriate treatment may reduce the risk of complications and limit mortality, also depending on the related comorbidity
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Het Ogilvie-syndroom bij oudere patienten met multiproblematiek
'Springer Science and Business Media LLC', 2014Co-Authors: Tan A.c., Olde Rikkert M.g.m., Groenen M.j.Abstract:Item does not contain fulltextTHE Ogilvie Syndrome IN ELDERLY PATIENTS WITH MULTIMORBIDITY: Two patients presented with the Ogilvie Syndrome which is an acute colonic pseudo-obstruction without any mechanical obstruction. Both patients suffered from multiple medical conditions such as infections, electrolyte disturbances and functional decline.The Ogilvie Syndrome is particularly seen in patients with multimorbidity who stay in the hospital or nursing home. The incidence of the Ogilvie Syndrome will probably increase because of ageing of our population and will be most prevalent in the frail elderly. The precise mechanism of this disease is still unclear, but there is evidence in the literature that the aetiology is multifactorial and runs via autonomic dysregulation of the colon.Early recognition and appropriate treatment may reduce the risk of complications and limit mortality, also depending on the related comorbidity
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Het Ogilvie-syndroom bij oudere patienten met multiproblematiek
'Springer Science and Business Media LLC', 2014Co-Authors: Tan A.c., Olde Rikkert M.g.m., Groenen M.j.Abstract:THE Ogilvie Syndrome IN ELDERLY PATIENTS WITH MULTIMORBIDITY: Two patients presented with the Ogilvie Syndrome which is an acute colonic pseudo-obstruction without any mechanical obstruction. Both patients suffered from multiple medical conditions such as infections, electrolyte disturbances and functional decline.The Ogilvie Syndrome is particularly seen in patients with multimorbidity who stay in the hospital or nursing home. The incidence of the Ogilvie Syndrome will probably increase because of ageing of our population and will be most prevalent in the frail elderly. The precise mechanism of this disease is still unclear, but there is evidence in the literature that the aetiology is multifactorial and runs via autonomic dysregulation of the colon.Early recognition and appropriate treatment may reduce the risk of complications and limit mortality, also depending on the related comorbidity
Sergio Javier Fernández Ortíz - One of the best experts on this subject based on the ideXlab platform.
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acute colonic pseudo obstruction Ogilvie Syndrome post renal transplantation
Boletín médico del Hospital Infantil de México, 2016Co-Authors: Erik Antonio Mier Escurra, Sergio Javier Fernández Ortíz, Talia Diaz Prieto, Guillermo Mier Saad, Alejandro Valdes CepedaAbstract:Abstract Background Acute colonic pseudo-obstruction, also known as Ogilvie Syndrome, is a rare gastrointestinal Syndrome in children. It is characterized by a marked dilatation of the colon evidenced by imaging and absence of mechanical obstruction. Patients typically present abdominal pain and distention, tympanic abdomen with peristalsis accompanied by nausea and vomiting. Up to 40% of patients can pass gas and have bowel movements. This Syndrome is very rare in pediatric patients, and no cases have been reported in a post-renal transplant pediatric patient. Case report A 13-year-old male patient with a medical history of psychomotor retardation due to perinatal asphyxia and chronic renal failure secondary to bilateral renal hypoplasia was treated with peritoneal dialysis for one year until kidney transplantation. Currently, he is under immunosuppressive regimen. His condition began with mild abdominal pain accompanied by semi-liquid stools, and progressive distention up to 78 cm of abdominal circumference in 72 hours. Image studies were performed. Managed with prokinetic drugs without any improvement. Two exploratory laparotomies observed flanges, without evidence of any mechanical obstruction. An abdominal magnetic resonance was performed, where important intestinal dilatation was observed and no evidence of mechanical obstruction. Ogilvie's Syndrome was diagnosed, and management with neostigmine was initiated, which led to symptom resolution. Conclusions This Syndrome is very rare in children. Therefore, there is little clinical suspicion and lack of management guidelines for diagnosis and treatment of patients of this age.
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Acute colonic pseudo-obstruction (Ogilvie Syndrome) post-renal transplant [Pseudo-obstrucción colónica aguda (síndrome de Ogilvie) post-trasplante renal]
'Elsevier BV', 2016Co-Authors: Sergio Javier Fernández Ortíz, Alejandro Valdes CepedaAbstract:Background Acute colonic pseudo-obstruction, also known as Ogilvie Syndrome, is a rare gastrointestinal Syndrome in children. It is characterized by a marked dilatation of the colon evidenced by imaging and absence of mechanical obstruction. Patients typically present with abdominal pain and distended, tympanic abdomen, with peristalsis present, accompanied by nausea and vomiting. Up to 40% of patients can pass gas and/or have bowel movements. We decide to report this case because this Syndrome is very rare in pediatric patients, and no cases have been reported in a post-renal transplant pediatric patient. Case report 13 year old male patient with past medical history of psychomotor retardation due to perinatal asphyxia and chronic renal failure secondary to bilateral renal hypoplasia. Treated with peritoneal dialysis for one year until kidney transplant was performed. Currently under immunosuppressive regime. He began his condition with mild abdominal pain accompanied by semi-liquid stools, and progressive distention up to 78\ua0cm of abdominal circumference in 72\ua0hours, so image studies were performed. Managed with prokinetic drugs without any improvement. Two exploratory laparotomies observed flanges, without evidence of any mechanical obstruction. An abdominal magnetic resonance was performed, where important intestinal dilatation was observed with no evidence of mechanical obstruction. Ogilvie Syndrome was diagnosed, so management with neostigmine was established, which led to symptom resolution. Conclusions This case is reported because this Syndrome is very rare in children, there is little clinical suspicion and lack of management guides for diagnosis and treatment in patients of this age. © 2016 Hospital Infantil de México Federico Góme
