Infantile hypertrophic pyloric stenosis is caused by hypertrophy and hyperplasia of the pyloric muscle in infants 2-8 weeks old, resulting in narrowing of the pyloric canal. Genetic studies have identified susceptibility loci and molecular studies show improper innervation of smooth muscle cells. It occurs in 1 in 500 live births but can be as high as 1 in 200 in some regions, affecting males more than females. Presentation includes projectile vomiting 30-60 minutes after feeding with hunger, weight loss, and dehydration. Ultrasound confirms diagnosis while pyloromyotomy via open or laparoscopic surgery effectively treats the condition with excellent prognosis.
Tracheoesophageal fistula (TEF) is an abnormal connection between the trachea and esophagus that occurs in approximately 1 in 3,500 births. It can be congenital or acquired. There are various types classified by the locations of connections between the trachea and esophagus. Surgical repair is usually required to close the abnormal connections. Nursing care focuses on preventing aspiration, maintaining adequate nutrition and hydration, clearing airways, monitoring for complications, and supporting parents through the critical situation.
This document discusses infantile hypertrophic pyloric stenosis (IHPS), a condition that causes forceful vomiting in young infants. It provides details on the epidemiology, risk factors, clinical presentation, diagnosis and treatment of IHPS. Ultrasound is highlighted as the preferred method for diagnosing IHPS due to its non-invasive nature, accuracy and ability to directly visualize the thickened pyloric muscle. The document outlines the ultrasound technique and criteria used to diagnose IHPS based on measurements of the pyloric wall thickness and length.
Tracheoesophageal fistula and esophageal atresia are birth defects where the esophagus fails to develop properly and separate from the trachea. This results in an abnormal connection between the trachea and esophagus (tracheoesophageal fistula) and a discontinuity in the esophageal lumen (esophageal atresia). Affected infants often experience respiratory distress, coughing, choking, and inability to feed properly. Diagnosis involves imaging and classification of the specific defects. Treatment involves supportive care, antibiotics, feeding strategies, and surgery to reconnect the esophagus.
Pyloric stenosis is a narrowing of the opening from the stomach to the small intestine caused by thickening of the pyloric muscle. It typically affects infants younger than 6 months old, and boys are more commonly affected than girls. The main symptoms are projectile vomiting shortly after feeding due to impaired emptying of food from the stomach. Treatment involves surgically cutting the thickened pyloric muscle to widen the opening.
Intussusception is the invagination of one part of the intestine into another. It most commonly occurs in infants and children between 6 months and 2 years of age. Ultrasound is the preferred method of diagnosis as it can clearly visualize the "coiled-spring" or "bull's-eye" pattern of intussusception. Non-operative reduction using hydrostatic or pneumatic enema under fluoroscopic or ultrasound guidance is the first-line treatment and has high success rates of 80-95%. Surgical intervention is needed if non-operative reduction fails or if there is evidence of intestinal ischemia or perforation.
This document discusses esophageal atresia, beginning with the embryology and classification. Esophageal atresia occurs in approximately 1 in 2500-3000 live births, and is slightly more common in males. It can be associated with other anomalies. The classification system describes types A through E, with type C being most common. Prenatal diagnosis is suggested by polyhydramnios and absent stomach bubble on ultrasound. Postnatal diagnosis involves x-rays and other imaging. Treatment involves surgically closing the tracheoesophageal fistula and reconnecting the esophagus.
A Tracheoesophageal fistula is a congenital disease. It is a acquired communication between the trachea and esophagus. Most of the patient with TEF are diagnosed immediately following after birth.TEF are often associated with life threatening complications.
Infantile hypertrophic pyloric stenosis is caused by hypertrophy and hyperplasia of the pyloric muscle in infants 2-8 weeks old, resulting in narrowing of the pyloric canal. Genetic studies have identified susceptibility loci and molecular studies show improper innervation of smooth muscle cells. It occurs in 1 in 500 live births but can be as high as 1 in 200 in some regions, affecting males more than females. Presentation includes projectile vomiting 30-60 minutes after feeding with hunger, weight loss, and dehydration. Ultrasound confirms diagnosis while pyloromyotomy via open or laparoscopic surgery effectively treats the condition with excellent prognosis.
Tracheoesophageal fistula (TEF) is an abnormal connection between the trachea and esophagus that occurs in approximately 1 in 3,500 births. It can be congenital or acquired. There are various types classified by the locations of connections between the trachea and esophagus. Surgical repair is usually required to close the abnormal connections. Nursing care focuses on preventing aspiration, maintaining adequate nutrition and hydration, clearing airways, monitoring for complications, and supporting parents through the critical situation.
This document discusses infantile hypertrophic pyloric stenosis (IHPS), a condition that causes forceful vomiting in young infants. It provides details on the epidemiology, risk factors, clinical presentation, diagnosis and treatment of IHPS. Ultrasound is highlighted as the preferred method for diagnosing IHPS due to its non-invasive nature, accuracy and ability to directly visualize the thickened pyloric muscle. The document outlines the ultrasound technique and criteria used to diagnose IHPS based on measurements of the pyloric wall thickness and length.
Tracheoesophageal fistula and esophageal atresia are birth defects where the esophagus fails to develop properly and separate from the trachea. This results in an abnormal connection between the trachea and esophagus (tracheoesophageal fistula) and a discontinuity in the esophageal lumen (esophageal atresia). Affected infants often experience respiratory distress, coughing, choking, and inability to feed properly. Diagnosis involves imaging and classification of the specific defects. Treatment involves supportive care, antibiotics, feeding strategies, and surgery to reconnect the esophagus.
Pyloric stenosis is a narrowing of the opening from the stomach to the small intestine caused by thickening of the pyloric muscle. It typically affects infants younger than 6 months old, and boys are more commonly affected than girls. The main symptoms are projectile vomiting shortly after feeding due to impaired emptying of food from the stomach. Treatment involves surgically cutting the thickened pyloric muscle to widen the opening.
Intussusception is the invagination of one part of the intestine into another. It most commonly occurs in infants and children between 6 months and 2 years of age. Ultrasound is the preferred method of diagnosis as it can clearly visualize the "coiled-spring" or "bull's-eye" pattern of intussusception. Non-operative reduction using hydrostatic or pneumatic enema under fluoroscopic or ultrasound guidance is the first-line treatment and has high success rates of 80-95%. Surgical intervention is needed if non-operative reduction fails or if there is evidence of intestinal ischemia or perforation.
This document discusses esophageal atresia, beginning with the embryology and classification. Esophageal atresia occurs in approximately 1 in 2500-3000 live births, and is slightly more common in males. It can be associated with other anomalies. The classification system describes types A through E, with type C being most common. Prenatal diagnosis is suggested by polyhydramnios and absent stomach bubble on ultrasound. Postnatal diagnosis involves x-rays and other imaging. Treatment involves surgically closing the tracheoesophageal fistula and reconnecting the esophagus.
A Tracheoesophageal fistula is a congenital disease. It is a acquired communication between the trachea and esophagus. Most of the patient with TEF are diagnosed immediately following after birth.TEF are often associated with life threatening complications.
Pyloric stenosis is a narrowing of the opening from the stomach to the small intestine caused by thickening of the pyloric muscle. It typically presents in infants as projectile vomiting after feeding. Diagnosis is usually made clinically based on symptoms and feeling an olive-sized mass in the abdomen. Treatment involves initially stabilizing the infant followed by surgery to cut the thickened pyloric muscle. With timely diagnosis and treatment, prognosis is excellent with complete relief of symptoms and normal development. Nurses play an important role in pre and post-operative care including monitoring temperature, IV fluids, pain, and for any surgical complications.
This document discusses meconium disease, specifically meconium ileus. Meconium ileus is a common cause of intestinal obstruction in newborns, accounting for 9-33% of cases. It is characterized by thick, viscous meconium that obstructs the distal ileum. Meconium ileus is often an early manifestation of cystic fibrosis. The document describes the clinical presentation of meconium ileus and methods of prenatal diagnosis using ultrasound. Complications can include volvulus, gangrene, atresia and perforation.
This document discusses tracheoesophageal fistula (TEF), including its definition, development, epidemiology, anatomical variations, pathophysiology, clinical manifestations, diagnosis, management, and nursing care. TEF is a congenital abnormality where the trachea and esophagus are connected. It develops due to incomplete separation of the trachea and esophagus during embryonic development. Clinical signs include drooling, choking, respiratory distress, inability to feed, and aspiration pneumonia. Treatment involves surgical repair to separate the trachea and esophagus.
Esophageal atresia with or without tracheoesophageal fistulaMohsin Ali
This document provides information on esophageal atresia, including:
- Esophageal atresia is a congenital condition where the esophagus is interrupted, sometimes accompanied by a tracheoesophageal fistula.
- Classification systems help determine prognosis and appropriate timing of repair (immediate, delayed, staged). Higher risk patients with factors like low birth weight or cardiac issues may benefit from delayed or staged repair.
- Associated anomalies occur in about 50% of cases, most commonly vertebral, anorectal, cardiovascular, and renal defects.
Kelly, a 6-month old infant, has been vomiting whenever she is fed for the past 2 weeks. Her parents noticed an olive-shaped mass in her abdomen. They took her to their local pediatrician. The pediatrician suspects Kelly may have hypertrophic pyloric stenosis based on her symptoms of vomiting after feeding and the presence of a pyloric mass.
This document discusses pediatric surgery and focuses on congenital hypertrophic pyloric stenosis (CHPS). It describes CHPS as a condition that affects babies between birth and 6 months, causing forceful vomiting. The pathology involves hypertrophy of the pylorus muscle layer. Clinical features include projectile vomiting. Investigation may include ultrasound and barium meal. Treatment is resuscitation followed by Ramestedt pyloromyotomy surgery to cut the thickened pylorus muscle layer. Complications can include perforation or wound infection but recurrence is rare.
This document discusses the history, types, diagnosis and management of intussusception. It notes that intussusception occurs most often in children under 2 years old and presents with abdominal pain and vomiting. Ultrasound is the primary diagnostic tool, showing a target or doughnut-shaped mass. Management involves attempting non-operative reduction with hydrostatic or pneumatic enemas under radiologic guidance. Surgery is reserved for failed non-operative reduction or if signs of bowel ischemia are present. Recurrence rates after initial reduction are approximately 5-20%.
This document discusses congenital hypertrophic pyloric stenosis (CHPS), a condition where the pyloric muscle thickens, obstructing food passage from stomach to small intestine. It affects young infants, more commonly males. Presentation includes projectile vomiting after feeding. Diagnosis involves abdominal ultrasound and upper GI study. Treatment is pyloromyotomy surgery to cut the thickened pyloric muscle. The document covers epidemiology, clinical features, diagnosis, treatment including surgical procedure and postoperative care of CHPS.
Pyloric stenosis is a condition where the pylorus, the opening from the stomach to the small intestine, becomes narrowed due to muscle thickening. This causes projectile vomiting after feeding as food cannot pass easily into the intestines. It typically affects young infants under 3 months of age. Treatment involves a pyloromyotomy surgery to cut the thickened muscle and allow food to pass through.
This document discusses intestinal atresias and meconium ileus. It begins by describing duodenal atresia and stenosis, including historical aspects, incidence, embryology, theories of development, classification, and associated anomalies. It then covers clinical features, diagnosis including imaging studies, and management including surgical techniques like duodenoduodenostomy. Post-operative care and long-term complications are also summarized. The document concludes with a brief section on jejunoileal atresia.
This document presents a case study on tracheoesophageal fistula (TEF). It begins with an introduction stating that TEF is a congenital abnormal connection between the trachea and esophagus. It is often diagnosed at birth and can cause life-threatening complications. The document then defines TEF and provides information on incidence, etiology, pathophysiology, signs and symptoms, diagnosis, management including pharmacologic and surgical approaches, nursing diagnoses, and complications. It aims to inform on the nature, causes, and treatment of TEF.
Duodenal atresia is a common cause of neonatal intestinal obstruction, affecting 1 in 6,000-10,000 births. It has a survival rate of around 95% and is associated with other anomalies in 50% of cases. It results from a failure of recanalization of the duodenum during embryonic development in the 6th week of gestation. Treatment involves NG/OG decompression, IV fluids, and temperature control followed by surgical duodenoduodenostomy once the infant is stabilized.
A 30-year-old female presented with acute left abdominal pain and nausea. Imaging showed an intussusception, which is when a segment of bowel invaginates into another segment, often causing obstruction. Intussusception is most common in children under 2 years old and is frequently idiopathic, while in adults it is often due to an underlying cause like tumors. Computed tomography is the most accurate way to diagnose intussusception based on its characteristic appearance.
Pyloric stenosis is a condition where the pylorus muscle becomes thickened, preventing food from exiting the stomach. It typically presents in infants in the first few months of life with projectile vomiting following feeding. Management involves initially trying smaller, more frequent feedings along with medications, and if that fails surgical pyloromyotomy is performed where the thickened pylorus muscle is incised to allow food passage.
This document discusses various types of intestinal obstructions in neonates. It describes high intestinal obstructions, which occur proximal to the ileum such as gastric, duodenal or jejunal obstructions. It also describes low intestinal obstructions, which occur distal to the ileum and in the colon. Specific causes of obstruction discussed include duodenal atresia, intestinal malrotation, necrotizing enterocolitis, meconium ileus and Hirschsprung's disease. Diagnosis involves abdominal x-rays and contrast studies to identify the location and cause of obstruction.
This document discusses the embryology, pathology, classification, diagnosis and treatment of tracheoesophageal fistula (TEF). It begins with a description of the embryological development of the esophagus and trachea. It then covers the pathology, classifications including Gross-Vogt and Waterston systems. It discusses the clinical findings and diagnosis of TEF. It concludes with descriptions of preoperative treatment and surgical repair techniques for TEF.
1) This case report describes the presentation and management of a 10-month-old boy with recurrent intussusception who presented with abdominal pain and vomiting.
2) Ultrasound was used to diagnose intussusception and showed characteristics of a "pseudokidney".
3) The patient underwent pneumatic reduction which was successful in treating the recurrent intussusception. Close monitoring was required after the procedure.
This document discusses atresia and stenosis of the colon. It begins by defining colonic atresia and stenosis, noting that atresia is congenital while stenosis can be congenital or acquired. It then discusses the incidence, associated conditions, clinical presentation, relevant anatomy, and indications for treatment of colonic atresia and stenosis. Colonic atresia is a rare birth defect that causes obstruction of the colon and presents in newborns with abdominal distension. Treatment involves relieving the obstruction through colostomy or resection.
Hirschsprung disease is a congenital disorder where the enteric nervous system fails to develop in parts of the colon, most commonly in the rectum. This leads to obstruction and complications like enterocolitis. The diagnosis is confirmed with biopsy showing lack of ganglion cells. Treatment involves surgical removal of the aganglionic segment and reconnection of the bowel, such as with a Swenson or Duhamel procedure. Early diagnosis and treatment are important to prevent complications.
common surgical problem in pediatrics done.pptxpapurva49
This document discusses several common surgical problems in children. It begins by explaining the need for pediatricians to have knowledge of these conditions. It then lists and provides brief overviews of various issues such as cleft lip/palate, gastroesophageal reflux disease, Hirschsprung's disease, intestinal malformations, hernias, and genitourinary problems. For several conditions, it describes symptoms, investigations, management, and associated abnormalities. Throughout, it includes diagrams and images to illustrate key points.
Pyloric stenosis is a narrowing of the opening from the stomach to the small intestine caused by thickening of the pyloric muscle. It typically presents in infants as projectile vomiting after feeding. Diagnosis is usually made clinically based on symptoms and feeling an olive-sized mass in the abdomen. Treatment involves initially stabilizing the infant followed by surgery to cut the thickened pyloric muscle. With timely diagnosis and treatment, prognosis is excellent with complete relief of symptoms and normal development. Nurses play an important role in pre and post-operative care including monitoring temperature, IV fluids, pain, and for any surgical complications.
This document discusses meconium disease, specifically meconium ileus. Meconium ileus is a common cause of intestinal obstruction in newborns, accounting for 9-33% of cases. It is characterized by thick, viscous meconium that obstructs the distal ileum. Meconium ileus is often an early manifestation of cystic fibrosis. The document describes the clinical presentation of meconium ileus and methods of prenatal diagnosis using ultrasound. Complications can include volvulus, gangrene, atresia and perforation.
This document discusses tracheoesophageal fistula (TEF), including its definition, development, epidemiology, anatomical variations, pathophysiology, clinical manifestations, diagnosis, management, and nursing care. TEF is a congenital abnormality where the trachea and esophagus are connected. It develops due to incomplete separation of the trachea and esophagus during embryonic development. Clinical signs include drooling, choking, respiratory distress, inability to feed, and aspiration pneumonia. Treatment involves surgical repair to separate the trachea and esophagus.
Esophageal atresia with or without tracheoesophageal fistulaMohsin Ali
This document provides information on esophageal atresia, including:
- Esophageal atresia is a congenital condition where the esophagus is interrupted, sometimes accompanied by a tracheoesophageal fistula.
- Classification systems help determine prognosis and appropriate timing of repair (immediate, delayed, staged). Higher risk patients with factors like low birth weight or cardiac issues may benefit from delayed or staged repair.
- Associated anomalies occur in about 50% of cases, most commonly vertebral, anorectal, cardiovascular, and renal defects.
Kelly, a 6-month old infant, has been vomiting whenever she is fed for the past 2 weeks. Her parents noticed an olive-shaped mass in her abdomen. They took her to their local pediatrician. The pediatrician suspects Kelly may have hypertrophic pyloric stenosis based on her symptoms of vomiting after feeding and the presence of a pyloric mass.
This document discusses pediatric surgery and focuses on congenital hypertrophic pyloric stenosis (CHPS). It describes CHPS as a condition that affects babies between birth and 6 months, causing forceful vomiting. The pathology involves hypertrophy of the pylorus muscle layer. Clinical features include projectile vomiting. Investigation may include ultrasound and barium meal. Treatment is resuscitation followed by Ramestedt pyloromyotomy surgery to cut the thickened pylorus muscle layer. Complications can include perforation or wound infection but recurrence is rare.
This document discusses the history, types, diagnosis and management of intussusception. It notes that intussusception occurs most often in children under 2 years old and presents with abdominal pain and vomiting. Ultrasound is the primary diagnostic tool, showing a target or doughnut-shaped mass. Management involves attempting non-operative reduction with hydrostatic or pneumatic enemas under radiologic guidance. Surgery is reserved for failed non-operative reduction or if signs of bowel ischemia are present. Recurrence rates after initial reduction are approximately 5-20%.
This document discusses congenital hypertrophic pyloric stenosis (CHPS), a condition where the pyloric muscle thickens, obstructing food passage from stomach to small intestine. It affects young infants, more commonly males. Presentation includes projectile vomiting after feeding. Diagnosis involves abdominal ultrasound and upper GI study. Treatment is pyloromyotomy surgery to cut the thickened pyloric muscle. The document covers epidemiology, clinical features, diagnosis, treatment including surgical procedure and postoperative care of CHPS.
Pyloric stenosis is a condition where the pylorus, the opening from the stomach to the small intestine, becomes narrowed due to muscle thickening. This causes projectile vomiting after feeding as food cannot pass easily into the intestines. It typically affects young infants under 3 months of age. Treatment involves a pyloromyotomy surgery to cut the thickened muscle and allow food to pass through.
This document discusses intestinal atresias and meconium ileus. It begins by describing duodenal atresia and stenosis, including historical aspects, incidence, embryology, theories of development, classification, and associated anomalies. It then covers clinical features, diagnosis including imaging studies, and management including surgical techniques like duodenoduodenostomy. Post-operative care and long-term complications are also summarized. The document concludes with a brief section on jejunoileal atresia.
This document presents a case study on tracheoesophageal fistula (TEF). It begins with an introduction stating that TEF is a congenital abnormal connection between the trachea and esophagus. It is often diagnosed at birth and can cause life-threatening complications. The document then defines TEF and provides information on incidence, etiology, pathophysiology, signs and symptoms, diagnosis, management including pharmacologic and surgical approaches, nursing diagnoses, and complications. It aims to inform on the nature, causes, and treatment of TEF.
Duodenal atresia is a common cause of neonatal intestinal obstruction, affecting 1 in 6,000-10,000 births. It has a survival rate of around 95% and is associated with other anomalies in 50% of cases. It results from a failure of recanalization of the duodenum during embryonic development in the 6th week of gestation. Treatment involves NG/OG decompression, IV fluids, and temperature control followed by surgical duodenoduodenostomy once the infant is stabilized.
A 30-year-old female presented with acute left abdominal pain and nausea. Imaging showed an intussusception, which is when a segment of bowel invaginates into another segment, often causing obstruction. Intussusception is most common in children under 2 years old and is frequently idiopathic, while in adults it is often due to an underlying cause like tumors. Computed tomography is the most accurate way to diagnose intussusception based on its characteristic appearance.
Pyloric stenosis is a condition where the pylorus muscle becomes thickened, preventing food from exiting the stomach. It typically presents in infants in the first few months of life with projectile vomiting following feeding. Management involves initially trying smaller, more frequent feedings along with medications, and if that fails surgical pyloromyotomy is performed where the thickened pylorus muscle is incised to allow food passage.
This document discusses various types of intestinal obstructions in neonates. It describes high intestinal obstructions, which occur proximal to the ileum such as gastric, duodenal or jejunal obstructions. It also describes low intestinal obstructions, which occur distal to the ileum and in the colon. Specific causes of obstruction discussed include duodenal atresia, intestinal malrotation, necrotizing enterocolitis, meconium ileus and Hirschsprung's disease. Diagnosis involves abdominal x-rays and contrast studies to identify the location and cause of obstruction.
This document discusses the embryology, pathology, classification, diagnosis and treatment of tracheoesophageal fistula (TEF). It begins with a description of the embryological development of the esophagus and trachea. It then covers the pathology, classifications including Gross-Vogt and Waterston systems. It discusses the clinical findings and diagnosis of TEF. It concludes with descriptions of preoperative treatment and surgical repair techniques for TEF.
1) This case report describes the presentation and management of a 10-month-old boy with recurrent intussusception who presented with abdominal pain and vomiting.
2) Ultrasound was used to diagnose intussusception and showed characteristics of a "pseudokidney".
3) The patient underwent pneumatic reduction which was successful in treating the recurrent intussusception. Close monitoring was required after the procedure.
This document discusses atresia and stenosis of the colon. It begins by defining colonic atresia and stenosis, noting that atresia is congenital while stenosis can be congenital or acquired. It then discusses the incidence, associated conditions, clinical presentation, relevant anatomy, and indications for treatment of colonic atresia and stenosis. Colonic atresia is a rare birth defect that causes obstruction of the colon and presents in newborns with abdominal distension. Treatment involves relieving the obstruction through colostomy or resection.
Hirschsprung disease is a congenital disorder where the enteric nervous system fails to develop in parts of the colon, most commonly in the rectum. This leads to obstruction and complications like enterocolitis. The diagnosis is confirmed with biopsy showing lack of ganglion cells. Treatment involves surgical removal of the aganglionic segment and reconnection of the bowel, such as with a Swenson or Duhamel procedure. Early diagnosis and treatment are important to prevent complications.
common surgical problem in pediatrics done.pptxpapurva49
This document discusses several common surgical problems in children. It begins by explaining the need for pediatricians to have knowledge of these conditions. It then lists and provides brief overviews of various issues such as cleft lip/palate, gastroesophageal reflux disease, Hirschsprung's disease, intestinal malformations, hernias, and genitourinary problems. For several conditions, it describes symptoms, investigations, management, and associated abnormalities. Throughout, it includes diagrams and images to illustrate key points.
The document discusses various pediatric gastrointestinal disorders including:
1. Duodenal atresia, malrotation with midgut volvulus, jejunal/ileal atresia as causes of intestinal obstruction.
2. Hirschsprung's disease, anorectal malformations, meconium ileus as other causes.
3. Signs, investigations, and management are described for different conditions like biliary atresia.
Anomalies of the Gastrointestinal Tract and Anterior Abdominal.ppthendra472440
suatu materi tentang kelainan anatomi sistem pencernan yg berhubungan dengan obstertri dan ginekologi. termasuk lambung, usus halus, usus besar, rektum dan anus. Dapat berguna untuk penapisan sebelum bayi lahir. Diharapkan dengan materi ini dapat meningkatkan pengetahuan mahasiswa dalam ilmu yang berkaitan dengan Gastrointestinal terpadu. digunakan pada masyarakat umum dan sekitarnya.
Hirschsprung's disease is a birth defect where parts of the intestine do not have nerve cells. This causes poor or no muscle movement in the affected area. The document discusses the causes, symptoms, tests used for diagnosis, surgical treatments like colostomy and resection of the affected bowel, potential complications, nursing care before and after surgery, and long-term prognosis. The key surgical procedures mentioned are Swenson's procedure, Duhamel's procedure and Soave's procedure.
Esophageal diseases .pdf by university of kufa college of medicinezahraa934924
This document provides information on various esophageal diseases. It begins with an introduction to the anatomy and function of the esophagus. It then discusses specific conditions such as gastroesophageal reflux disease (GERD), infectious esophagitis, corrosive esophagitis, pills esophagitis, eosinophilic esophagitis, achalasia, and diffuse esophageal spasm. For each condition, it provides details on pathophysiology, clinical features, investigations, management, and complications. The document also includes tables of contents and section headings to organize the various topics.
Seminar presentation by 5th year Medical Student under the supervision of a pediatric surgery specialist from HRPZ II. Reference as mentioned in the slide.
Presentation1.pptx, radiological imaging of large bowel diseasesAbdellah Nazeer
This document discusses congenital anomalies and diseases of the large bowel. It begins by describing congenital abnormalities that can cause obstruction in neonates and the importance of radiological imaging to diagnose the location and cause. It then discusses different types of intestinal obstructions and how radiography and contrast enema exams are used to further evaluate obstructions and make a specific diagnosis. Examples of different congenital anomalies and diseases seen on imaging are also presented, including colonic atresia, meconium ileus, Hirschsprung disease, and colon cancer.
This document discusses intestinal obstruction, including its causes, classifications, symptoms, diagnosis and treatment. Some key points:
- Intestinal obstruction can be caused by adhesions, hernias, tumors, strictures and more. It is classified by the obstructed site and presence of blood flow issues.
- Symptoms include pain, vomiting, constipation and distension. Signs depend on obstruction location and duration. Strangulated obstructions require urgent surgery to prevent tissue death.
- Diagnosis involves medical history, physical exam, imaging like x-rays and CT scans. Treatment involves resuscitation, nasogastric drainage, and surgery to relieve the obstruction and address the underlying cause. S
This document discusses several common surgical emergencies that can occur in newborns, including abdominal wall defects like omphalocele and gastroschisis, intestinal obstructions from conditions like duodenal and jejunal atresia, and anomalies such as Hirschsprung's disease. It provides details on the presentation, evaluation, and management of each condition. Common signs include vomiting, abdominal distension, and failure to pass stool or meconium. Diagnosis involves imaging studies and sometimes biopsies, while treatment consists of resuscitation, antibiotics, gastric decompression, and often surgery to correct the underlying abnormality.
Dysphagia, or difficulty swallowing, can be caused by issues with the esophagus. The document discusses several diseases and conditions that cause dysphagia by obstructing the esophagus, including achalasia, esophageal cancer, and reflux esophagitis. It provides details on symptoms, diagnostics, and treatment for each condition. Esophageal spasms, tumors, diverticula, strictures, and foreign bodies can also obstruct the esophagus and cause dysphagia. The document examines each of these conditions and how they impact swallowing.
Presentation1, radiological imaging of hirshsprung disease.Abdellah Nazeer
Hirschsprung disease is a congenital disorder causing colonic obstruction. It results from the absence of ganglion cells in portions of the colon and rectum. This document discusses the epidemiology, clinical presentation, pathology, diagnosis and radiological findings of Hirschsprung disease. Key points include that it typically presents in newborn infants as failure to pass meconium. Diagnosis involves rectal biopsy and contrast enema to identify the transition zone between normal and aganglionic segments. Radiography may show dilated bowel and a narrow rectum. Barium enema can further define the transition zone location.
Hirschsprung's disease is a congenital disorder where there is an absence of ganglion cells in the distal colon, resulting in functional obstruction. It occurs in around 1 in 5000 live births and is more common in males. The classic presentation is constipation since birth. Diagnosis involves rectal biopsy and anorectal manometry. Treatment is surgical resection of the aganglionic segment and pull-through of the proximal ganglionic colon, with various procedures available. Complications can include infection, bleeding, stricture formation, and enterocolitis.
This document provides an overview of inguinal and scrotal disorders including anatomy, hernias, undescended testes, hydroceles, and other conditions. It begins with the anatomy of the inguinal region including the inguinal canal, spermatic cord, and Hesselbach's triangle. Inguinal hernias are then discussed including definitions, classifications, risk factors, presentations, investigations, differential diagnoses, and surgical management. Undescended testes and hydroceles are also summarized outlining definitions, epidemiology, presentations, investigations, and treatment approaches.
This presentation describes the total and partial intestinal atresia, its clinical features and diagnosis. in addition, this presentation include the definition of esophageal atresia, its classification, diagnosis and treatment.
Tracheo-oesophageal fistula and oesophagal atresia are birth defects where the esophagus does not form properly, either failing to connect to the stomach or connecting abnormally to the trachea. They occur in about 1 in 3500 births. Surgical intervention is required to divide any abnormal connections or perform anastomosis to reconnect the esophagus. Nursing care focuses on preventing aspiration, maintaining nutrition via feeding tubes, and managing pain and comfort after surgery. Complications can include tracheomalacia, anastomotic leaks, strictures, and reflux.
Delayed passage of meconium can be caused by several intestinal obstructions and diseases. It is suspected in full-term infants who do not pass meconium in the first 24 hours and in premature infants who delay passage for over a week. Diagnostic workup includes abdominal x-rays, ultrasound, and contrast studies to locate the obstruction. Management requires gastric decompression, fluid resuscitation to address dehydration, and monitoring of electrolytes and glucose levels which may become imbalanced. The cause is determined based on the presentation and imaging findings, and treatment involves surgery for structural issues or supportive care for medical conditions.
Hirschsprung Disease is a birth defect characterized by the absence of ganglion cells in parts of the colon, resulting in inadequate bowel motility. It occurs in about 1 in 5000 live births and is diagnosed most often in the neonatal period in males. Symptoms include constipation, abdominal distension, and failure to thrive. Diagnosis involves tests like barium enema and rectal biopsy. Treatment begins with supportive care and may involve surgery to remove the affected colon segment. Nursing care focuses on managing symptoms, providing comfort, teaching family, and preventing complications.
This document provides an overview of common gastrointestinal abnormalities seen in pediatric patients. It discusses conditions such as vomiting, hypertrophic pyloric stenosis, duodenal atresia, intestinal malrotation, midgut volvulus, meconium ileus, necrotizing enterocolitis, Meckel's diverticulum, intussusception, appendicitis, Hirschsprung disease, mesenteric cysts, and anorectal malformations. For each condition, it provides a brief definition and discussion of relevant physical exam findings, diagnostic approaches, and treatment considerations for pediatric patients.
Similar to Radiology and contrast studies in newborns [autosaved] (20)
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
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8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Does Over-Masturbation Contribute to Chronic Prostatitis.pptxwalterHu5
In some case, your chronic prostatitis may be related to over-masturbation. Generally, natural medicine Diuretic and Anti-inflammatory Pill can help mee get a cure.
7. Abdominal radiograph
In case of intestinal onsruction first line of investigation is always Abdominal
radiograph provided enough time given to intestine filled with air.
Normal air progression time is as follows:
Birth Stomach
1 hour Duodenum
3 hour Proximal small bowel
12 hour Almost whole small bowel
24 hour Rectum
8. Bowel gas Patterns on Radiograph
Dilatation
Number of loops
Small bowel or large gut
Air filled rectum
Pnuematosis intestinalis
Free air/ pneumoperitonium
12. Air filled rectum
Radiograph of Meconium ileus
By 24 hr of life usually rectum filled
With air
If no air is there
Suspicion of HD and meconium ileus
must be in mind
17. Barium Contrast studies
Indications
GI Tract Imaging
Barium swallow- to study pharynx and esophagus
Barium meal- for lower esophagus, stomach and duodenum
Barium follow through- to study small intestine
Barium enema- for large intestine and rectum
Suspected H-type Fistula
Suspected esophageal perforation
Suspected GER
23. Small Left colon syndrome???
Meconium plug syndrome is also known
as small left colon syndrome.
Meconium plugging in the left colon occurs
when the colon is functionally immature with
little motility.
There is an association with maternal diabetes
and drug use in pregnancy.
The condition is temporarily and when the
meconium plugs resolve, the colon distends
normally and functions normally.
The neonate is otherwise healthy and
there is no association with cystic fibrosis.
There is no air in the rectum on the radiograph.
Colon enema shows a normal rectal diameter
which excludes Hirschsprung disease.
A microcolon is absent.
24. Hirschsprung disease
In Hirschsprung disease ganglion cells are absent
in the distal part of the colon.
Because the intestinal ganglion cells migrate in a
craniocaudal direction, the area of aganglionosis always
involves the rectum.
More extensive disease extends orally in a contiguous fashion.
The involved bowel has a small diameter and
the bowel proximal to the affected segment is dilated.
In Hirschsprung disease the ratio between the denervated
and the non-affected bowel is <1.
25. Hirschsprung disease
Start the enema in the lateral position to evaluate the rectum.
Save cine images from the first contrast injection,
as with progressive filling signs can become obscured
by too much bowel distention.
Normally the rectum should be wider than the sigmoid.
The image shows an abnormal recto-sigmoid index <1.