The Experts below are selected from a list of 480 Experts worldwide ranked by ideXlab platform
A Dickgiesser - One of the best experts on this subject based on the ideXlab platform.
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ultrasonic diagnosis of fetal ascites with polyhydramnios resulting from partial small Intestine Atresia and secondary intestinal wall perforation
Ultraschall in Der Medizin, 2008Co-Authors: W Hatzmann, U Dickgiesser, A DickgiesserAbstract:: A primigravida was admitted to hospital in the 31st week of pregnancy after normal pregnancy course, with premature rupture of the amnion. Ultrasonography revealed a marked fetal ascites as well as polyhydramnion. Pregnancy was terminated via Caesarean section because of threatening intrauterine asphyxia. The asphyctic, hypotonic infant, which did not show any visible malformation, was intubated and the ascites was punctured. After a brief recovery, the infant died 24 hours post partum. Autopsy revealed partial Atresia of the small Intestine with secondary perforation of the intestinal wall, as well as a fibrinous-purulent peritonitis. Pathogenesis of the foetal ascites, as well as the possibilities of diagnosis via sonography in case of fetal malformations, are discussed on the basis of the present case and previous literature.
W Hatzmann - One of the best experts on this subject based on the ideXlab platform.
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ultrasonic diagnosis of fetal ascites with polyhydramnios resulting from partial small Intestine Atresia and secondary intestinal wall perforation
Ultraschall in Der Medizin, 2008Co-Authors: W Hatzmann, U Dickgiesser, A DickgiesserAbstract:: A primigravida was admitted to hospital in the 31st week of pregnancy after normal pregnancy course, with premature rupture of the amnion. Ultrasonography revealed a marked fetal ascites as well as polyhydramnion. Pregnancy was terminated via Caesarean section because of threatening intrauterine asphyxia. The asphyctic, hypotonic infant, which did not show any visible malformation, was intubated and the ascites was punctured. After a brief recovery, the infant died 24 hours post partum. Autopsy revealed partial Atresia of the small Intestine with secondary perforation of the intestinal wall, as well as a fibrinous-purulent peritonitis. Pathogenesis of the foetal ascites, as well as the possibilities of diagnosis via sonography in case of fetal malformations, are discussed on the basis of the present case and previous literature.
Haddy Alas - One of the best experts on this subject based on the ideXlab platform.
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tethered cord syndrome in the united states cluster analysis of presenting anomalies and associated
Bulletin of the Hospital for Joint Disease, 2020Co-Authors: Samantha R Horn, Michael J Moses, Dennis Vasquezmontes, Aaron Hockley, Gregory W Poorman, Cole Bortz, Frank A Segreto, Avery Brown, Katherine E Pierce, Haddy AlasAbstract:PURPOSE Tethered cord syndrome (TCS) is an occult spinal dysraphism that includes low lying conus, tight filum terminale, lipomeningomyelocele, split cord malformations, dermal sinus tracts, and dermoids. This congenital disorder has been associated with musculoskeletal, neurological, and gastrointestinal abnormalities. This study presents a retrospective review of the prospectively collected data of TCS patients and their concurrent diagnoses or associated anomalies. METHODS The National Inpatient Sample (NIS) database from 2003 to 2012 was used for data collection. Hospital- and year-adjusted weights allowed for accurate assessment of the incidence of TCS, as well as cardiac and gastrointestinal (GI) and genitourinary (GU) anomalies. K-means clustering analysis was run to discover patterns of concurrent cardiac, GI, GU, and other system anomalies in TCS patients. RESULTS A total of 13,470 discharges with a diagnosis of TCS were identified in the NIS database, and at least one additional anomaly was identified in 40.7% of TCS patients. The most common secondary anomalies by system were: spine (24.48%), cardiac (6.27%), and urinary (5.37%). For patients with multiple anomalies, the most common combinations were GI and cardiac (4.55%), urinary and GI (4.26%), and urinary and cardiac (4.19%). The most common spinal association was spina bifida (13.65%). The most common neurological or musculoskeletal anomaly was any VACTERL association (13.45%). The top relation in GI and GU anomalies was cervix and female genitalia anomalies (69.1%). The most common specific anomalies were spina bifida, large Intestine Atresia, Rubenstein-Taybi syndrome, and atrial and ventral septal defects. CONCLUSION This study provides a nationwide prospective on congenital anomalies and concurrent conditions present in tethered cord syndrome patients in the United States and demonstrates that 40.7% of TCS patients have at least one associated anomaly. The most common congenital anomalies studied were spina bifida, urogenital with or without cardiac septal defects, and cystourethral anomaly or cystic kidney disease with or without large intestinal Atresia.
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tethered cord syndrome in the united states cluster analysis of presenting anomalies and associated conditions
Bulletin of the Hospital for Joint Diseases, 2020Co-Authors: Samantha R Horn, Michael J Moses, Dennis Vasquezmontes, Aaron Hockley, Gregory W Poorman, Cole Bortz, Frank A Segreto, Avery Brown, Katherine E Pierce, Haddy AlasAbstract:Purpose Tethered cord syndrome (TCS) is an occult spinal dysraphism that includes low lying conus, tight filum terminale, lipomeningomyelocele, split cord malformations, dermal sinus tracts, and dermoids. This congenital disorder has been associated with musculoskeletal, neurological, and gastrointestinal abnormalities. This study presents a retrospective review of the prospectively collected data of TCS patients and their concurrent diagnoses or associated anomalies. Methods The National Inpatient Sample (NIS) database from 2003 to 2012 was used for data collection. Hospital- and year-adjusted weights allowed for accurate assessment of the incidence of TCS, as well as cardiac and gastrointestinal (GI) and genitourinary (GU) anomalies. K-means clustering analysis was run to discover patterns of concurrent cardiac, GI, GU, and other system anomalies in TCS patients. Results A total of 13,470 discharges with a diagnosis of TCS were identified in the NIS database, and at least one additional anomaly was identified in 40.7% of TCS patients. The most common secondary anomalies by system were: spine (24.48%), cardiac (6.27%), and urinary (5.37%). For patients with multiple anomalies, the most common combinations were GI and cardiac (4.55%), urinary and GI (4.26%), and urinary and cardiac (4.19%). The most common spinal association was spina bifida (13.65%). The most common neurological or musculoskeletal anomaly was any VACTERL association (13.45%). The top relation in GI and GU anomalies was cervix and female genitalia anomalies (69.1%). The most common specific anomalies were spina bifida, large Intestine Atresia, Rubenstein-Taybi syndrome, and atrial and ventral septal defects. Conclusion This study provides a nationwide prospective on congenital anomalies and concurrent conditions present in tethered cord syndrome patients in the United States and demonstrates that 40.7% of TCS patients have at least one associated anomaly. The most common congenital anomalies studied were spina bifida, urogenital with or without cardiac septal defects, and cystourethral anomaly or cystic kidney disease with or without large intestinal Atresia.
U Dickgiesser - One of the best experts on this subject based on the ideXlab platform.
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ultrasonic diagnosis of fetal ascites with polyhydramnios resulting from partial small Intestine Atresia and secondary intestinal wall perforation
Ultraschall in Der Medizin, 2008Co-Authors: W Hatzmann, U Dickgiesser, A DickgiesserAbstract:: A primigravida was admitted to hospital in the 31st week of pregnancy after normal pregnancy course, with premature rupture of the amnion. Ultrasonography revealed a marked fetal ascites as well as polyhydramnion. Pregnancy was terminated via Caesarean section because of threatening intrauterine asphyxia. The asphyctic, hypotonic infant, which did not show any visible malformation, was intubated and the ascites was punctured. After a brief recovery, the infant died 24 hours post partum. Autopsy revealed partial Atresia of the small Intestine with secondary perforation of the intestinal wall, as well as a fibrinous-purulent peritonitis. Pathogenesis of the foetal ascites, as well as the possibilities of diagnosis via sonography in case of fetal malformations, are discussed on the basis of the present case and previous literature.
Samantha R Horn - One of the best experts on this subject based on the ideXlab platform.
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tethered cord syndrome in the united states cluster analysis of presenting anomalies and associated
Bulletin of the Hospital for Joint Disease, 2020Co-Authors: Samantha R Horn, Michael J Moses, Dennis Vasquezmontes, Aaron Hockley, Gregory W Poorman, Cole Bortz, Frank A Segreto, Avery Brown, Katherine E Pierce, Haddy AlasAbstract:PURPOSE Tethered cord syndrome (TCS) is an occult spinal dysraphism that includes low lying conus, tight filum terminale, lipomeningomyelocele, split cord malformations, dermal sinus tracts, and dermoids. This congenital disorder has been associated with musculoskeletal, neurological, and gastrointestinal abnormalities. This study presents a retrospective review of the prospectively collected data of TCS patients and their concurrent diagnoses or associated anomalies. METHODS The National Inpatient Sample (NIS) database from 2003 to 2012 was used for data collection. Hospital- and year-adjusted weights allowed for accurate assessment of the incidence of TCS, as well as cardiac and gastrointestinal (GI) and genitourinary (GU) anomalies. K-means clustering analysis was run to discover patterns of concurrent cardiac, GI, GU, and other system anomalies in TCS patients. RESULTS A total of 13,470 discharges with a diagnosis of TCS were identified in the NIS database, and at least one additional anomaly was identified in 40.7% of TCS patients. The most common secondary anomalies by system were: spine (24.48%), cardiac (6.27%), and urinary (5.37%). For patients with multiple anomalies, the most common combinations were GI and cardiac (4.55%), urinary and GI (4.26%), and urinary and cardiac (4.19%). The most common spinal association was spina bifida (13.65%). The most common neurological or musculoskeletal anomaly was any VACTERL association (13.45%). The top relation in GI and GU anomalies was cervix and female genitalia anomalies (69.1%). The most common specific anomalies were spina bifida, large Intestine Atresia, Rubenstein-Taybi syndrome, and atrial and ventral septal defects. CONCLUSION This study provides a nationwide prospective on congenital anomalies and concurrent conditions present in tethered cord syndrome patients in the United States and demonstrates that 40.7% of TCS patients have at least one associated anomaly. The most common congenital anomalies studied were spina bifida, urogenital with or without cardiac septal defects, and cystourethral anomaly or cystic kidney disease with or without large intestinal Atresia.
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tethered cord syndrome in the united states cluster analysis of presenting anomalies and associated conditions
Bulletin of the Hospital for Joint Diseases, 2020Co-Authors: Samantha R Horn, Michael J Moses, Dennis Vasquezmontes, Aaron Hockley, Gregory W Poorman, Cole Bortz, Frank A Segreto, Avery Brown, Katherine E Pierce, Haddy AlasAbstract:Purpose Tethered cord syndrome (TCS) is an occult spinal dysraphism that includes low lying conus, tight filum terminale, lipomeningomyelocele, split cord malformations, dermal sinus tracts, and dermoids. This congenital disorder has been associated with musculoskeletal, neurological, and gastrointestinal abnormalities. This study presents a retrospective review of the prospectively collected data of TCS patients and their concurrent diagnoses or associated anomalies. Methods The National Inpatient Sample (NIS) database from 2003 to 2012 was used for data collection. Hospital- and year-adjusted weights allowed for accurate assessment of the incidence of TCS, as well as cardiac and gastrointestinal (GI) and genitourinary (GU) anomalies. K-means clustering analysis was run to discover patterns of concurrent cardiac, GI, GU, and other system anomalies in TCS patients. Results A total of 13,470 discharges with a diagnosis of TCS were identified in the NIS database, and at least one additional anomaly was identified in 40.7% of TCS patients. The most common secondary anomalies by system were: spine (24.48%), cardiac (6.27%), and urinary (5.37%). For patients with multiple anomalies, the most common combinations were GI and cardiac (4.55%), urinary and GI (4.26%), and urinary and cardiac (4.19%). The most common spinal association was spina bifida (13.65%). The most common neurological or musculoskeletal anomaly was any VACTERL association (13.45%). The top relation in GI and GU anomalies was cervix and female genitalia anomalies (69.1%). The most common specific anomalies were spina bifida, large Intestine Atresia, Rubenstein-Taybi syndrome, and atrial and ventral septal defects. Conclusion This study provides a nationwide prospective on congenital anomalies and concurrent conditions present in tethered cord syndrome patients in the United States and demonstrates that 40.7% of TCS patients have at least one associated anomaly. The most common congenital anomalies studied were spina bifida, urogenital with or without cardiac septal defects, and cystourethral anomaly or cystic kidney disease with or without large intestinal Atresia.
