Posterior urethral valves are congenital anomalies that can cause obstruction of urine flow from the bladder. If not treated, they can lead to damage of the lower and upper urinary tract, including renal dysfunction. Early diagnosis through antenatal ultrasound and treatment after birth through valve ablation or vesicostomy can help prevent long term complications. Prognosis depends on factors like age of presentation, presence of reflux, and renal function as assessed by creatinine levels.
Ureteropelvic junction obstruction by\ Eman Salman
It was used for student presentation in Urology course rotation
I Hope you find what is helpful for your knowledge ♥
Management of pelviureteric junction obstruction onyeze copyChigozie Onyeze
This document provides an outline and overview of pelviureteric junction obstruction. It discusses the epidemiology, relevant anatomy, etiology, pathophysiology, clinical features, investigations, and management including surgical and non-surgical treatment options. The standard surgical procedure for repair is the Anderson-Hynes dismembered pyeloplasty technique, which involves excision of the narrowed segment and anastomosis of the renal pelvis to the ureter. Other approaches include endoscopic techniques, laparoscopic pyeloplasty, and robotic-assisted surgery. Proper pre-operative evaluation and post-operative care are important for optimal outcomes.
Congenital genitourinary disorders are birth defects of the kidneys and urinary tract that occur in about 3-6 per 1000 live births. Some common disorders include renal agenesis, hydronephrosis, posterior urethral valves, hypospadias, and Wilm's tumor. Symptoms vary depending on the specific disorder but can include urinary tract infections, blood in the urine, pain, and kidney failure. Treatment involves surgery to correct structural abnormalities, antibiotics to treat infections, and chemotherapy for Wilm's tumor. Nursing care focuses on monitoring the child, preventing infections, providing comfort, and educating parents.
Posterior urethral valves are congenital anomalies that obstruct the urethra in males. They were first recognized in the 18th century but were not diagnosed endoscopically until the early 20th century. PUVs cause damage to the urinary tract including the bladder, ureters, and kidneys due to increased pressure from blocked urine flow. Treatment involves endoscopic resection of the valves to restore urine flow. Long term follow up is needed due to risks of bladder dysfunction, infections, and renal impairment. Prognosis depends on factors like age of presentation, presence of reflux, and kidney function.
Ureteropelvic junction obstruction in childrenMUSTAFA MAJID
UPJ obstruction occurs when urine cannot drain properly from the renal pelvis due to inadequate drainage at the ureteropelvic junction. This causes backup of urine in the kidney that can damage the kidney over time. Surgical correction via pyeloplasty is usually indicated to relieve the obstruction and improve renal function. Dismembered pyeloplasty is the standard surgical procedure for repair of UPJ obstruction.
This document provides an overview of congenital ureteropelvic junction (UPJ) obstruction. It begins with definitions and epidemiology, noting it is the most common cause of antenatally detected hydronephrosis. The pathophysiology section describes how partial or complete obstruction of urine flow at the UPJ can lead to hydronephrosis. Causes may be intrinsic stenosis or extrinsic compression at the UPJ. Clinical presentation varies from incidental finding to symptoms like urinary tract infections. Diagnosis involves imaging like ultrasound and diuretic renography. Management options include conservative observation or surgical interventions like open or laparoscopic pyeloplasty depending on severity.
Posterior urethral valves is a congenital condition caused by abnormal membranes in the proximal urethra that obstruct the flow of urine. It most commonly presents in infancy with failure to pass urine and is diagnosed using imaging like ultrasound and voiding cystourethrography. Treatment involves surgical ablation of the valves via cystoscopy to restore urinary flow and halt renal damage. Prognosis depends on factors like age at diagnosis and degree of renal dysfunction, as patients may develop lifelong complications due to the original renal insults.
Posterior urethral valves are congenital anomalies that can cause obstruction of urine flow from the bladder. If not treated, they can lead to damage of the lower and upper urinary tract, including renal dysfunction. Early diagnosis through antenatal ultrasound and treatment after birth through valve ablation or vesicostomy can help prevent long term complications. Prognosis depends on factors like age of presentation, presence of reflux, and renal function as assessed by creatinine levels.
Ureteropelvic junction obstruction by\ Eman Salman
It was used for student presentation in Urology course rotation
I Hope you find what is helpful for your knowledge ♥
Management of pelviureteric junction obstruction onyeze copyChigozie Onyeze
This document provides an outline and overview of pelviureteric junction obstruction. It discusses the epidemiology, relevant anatomy, etiology, pathophysiology, clinical features, investigations, and management including surgical and non-surgical treatment options. The standard surgical procedure for repair is the Anderson-Hynes dismembered pyeloplasty technique, which involves excision of the narrowed segment and anastomosis of the renal pelvis to the ureter. Other approaches include endoscopic techniques, laparoscopic pyeloplasty, and robotic-assisted surgery. Proper pre-operative evaluation and post-operative care are important for optimal outcomes.
Congenital genitourinary disorders are birth defects of the kidneys and urinary tract that occur in about 3-6 per 1000 live births. Some common disorders include renal agenesis, hydronephrosis, posterior urethral valves, hypospadias, and Wilm's tumor. Symptoms vary depending on the specific disorder but can include urinary tract infections, blood in the urine, pain, and kidney failure. Treatment involves surgery to correct structural abnormalities, antibiotics to treat infections, and chemotherapy for Wilm's tumor. Nursing care focuses on monitoring the child, preventing infections, providing comfort, and educating parents.
Posterior urethral valves are congenital anomalies that obstruct the urethra in males. They were first recognized in the 18th century but were not diagnosed endoscopically until the early 20th century. PUVs cause damage to the urinary tract including the bladder, ureters, and kidneys due to increased pressure from blocked urine flow. Treatment involves endoscopic resection of the valves to restore urine flow. Long term follow up is needed due to risks of bladder dysfunction, infections, and renal impairment. Prognosis depends on factors like age of presentation, presence of reflux, and kidney function.
Ureteropelvic junction obstruction in childrenMUSTAFA MAJID
UPJ obstruction occurs when urine cannot drain properly from the renal pelvis due to inadequate drainage at the ureteropelvic junction. This causes backup of urine in the kidney that can damage the kidney over time. Surgical correction via pyeloplasty is usually indicated to relieve the obstruction and improve renal function. Dismembered pyeloplasty is the standard surgical procedure for repair of UPJ obstruction.
This document provides an overview of congenital ureteropelvic junction (UPJ) obstruction. It begins with definitions and epidemiology, noting it is the most common cause of antenatally detected hydronephrosis. The pathophysiology section describes how partial or complete obstruction of urine flow at the UPJ can lead to hydronephrosis. Causes may be intrinsic stenosis or extrinsic compression at the UPJ. Clinical presentation varies from incidental finding to symptoms like urinary tract infections. Diagnosis involves imaging like ultrasound and diuretic renography. Management options include conservative observation or surgical interventions like open or laparoscopic pyeloplasty depending on severity.
Posterior urethral valves is a congenital condition caused by abnormal membranes in the proximal urethra that obstruct the flow of urine. It most commonly presents in infancy with failure to pass urine and is diagnosed using imaging like ultrasound and voiding cystourethrography. Treatment involves surgical ablation of the valves via cystoscopy to restore urinary flow and halt renal damage. Prognosis depends on factors like age at diagnosis and degree of renal dysfunction, as patients may develop lifelong complications due to the original renal insults.
PUJ obstruction is a restriction of urine flow from the renal pelvis to the ureter. It can be congenital or acquired, with congenital being one of the most common causes of antenatal hydronephrosis. Diagnosis involves ultrasonography, VCUG, diuretic renography and other imaging modalities to determine severity and presence of associated issues. Treatment depends on severity but typically involves surgical intervention like open or laparoscopic pyeloplasty to resect and reanastomose the obstructed segment if drainage is significantly impaired or renal growth is poor. Postoperative follow up with imaging is important to monitor repair.
This document provides an overview of common urologic emergencies and their management. It discusses renal colic caused by kidney stones, including pain management with NSAIDs and opioids. It also covers acute urinary retention, priapism, hematuria, and anuria. For each condition, it outlines evaluation, differential diagnosis, and treatment approaches including medical expulsive therapy, ureteral stenting, and surgical procedures.
Hydronephrosis is the dilation of the renal pelvis and calyces due to partial or intermittent obstruction of urine flow. It is usually caused by blockages or reflux in the urinary tract. Common causes in children include vesicoureteral reflux, ureteropelvic junction obstruction, and posterior urethral valves. Diagnosis involves renal ultrasound and tests to assess kidney function. Treatment depends on the severity and underlying cause, ranging from observation to surgery to correct blockages or reflux. Complications can include urinary tract infections, kidney damage, and renal failure if not properly treated.
PUJO is an obstruction of the proximal ureter at the junction with the renal pelvis. It is most common in childhood, affecting 1 in 1000 children, with boys more commonly affected than girls. Presentation includes flank pain, flank mass, nausea, vomiting, recurrent UTIs, and hematuria. Diagnosis involves blood tests, urine tests, ultrasounds, CT scans, nuclear scans, and retrograde pyelography. Treatment depends on symptoms and impairment - watchful waiting may be sufficient, but surgery like pyeloplasty is often needed and has a high success rate of 90-95%.
Etiopathogenesis, Evaluation & Management of Posterior Urethral ValveShubham Lavania
This document discusses posterior urethral valves (PUV), including their etiology, classification, pathophysiology, clinical presentation, diagnosis, and management. PUV are congenital obstructions of the posterior urethra that commonly cause urinary outflow obstruction in boys. Type I valves are the most common. Initial management involves bladder drainage and antibiotics. Surgical valve ablation is usually curative, but long-term sequelae like renal disease are significant due to the primitive tissue injury caused by the obstruction.
This document summarizes benign prostatic hyperplasia (BPH). It finds that the incidence of BPH increases with age, affecting 20% of men aged 41-50 and over 90% of men over 80. Risk factors include genetics and race. BPH causes both obstructive symptoms like weak urinary stream and irritative symptoms like frequent urination. Treatment options range from watchful waiting for mild cases to drug therapies like alpha blockers and 5-alpha reductase inhibitors to surgical procedures like transurethral resection of the prostate. Minimally invasive procedures also exist like laser therapy, transurethral vaporization of the prostate, and transurethral needle ablation of the prostate.
Most common site of urinary tract obstruction in children
-Majority are discovered antenatal
-1:800-1500 pregnancies
-80% antenatal hydronephrosis
-2:1 boys : girls
-2/3 on the left
-10-40% bilateral
Pelvi ureteric junction obstruction in childrenAseesh Varma
This document discusses pelvi-ureteral junction obstruction (PUJO). It begins by describing fetal urine production and the role of amniotic fluid in lung development. It then covers the causes of PUJO, which can be intrinsic due to abnormal development of the ureteral bud, or extrinsic due to compression from blood vessels. Clinical presentation varies from antenatal detection of hydronephrosis to abdominal pain or urinary tract infections in older children. Diagnosis involves ultrasound to assess renal pelvis dilation and thinning of parenchyma over time.
Pathophysioogy of urinary tract obstruction bassem presentationfreeburn simunchembu
This document discusses obstructive nephropathy and hydronephrosis. It defines key terms and outlines the prevalence, classifications, causes, pathophysiology, diagnosis and management of obstructive kidney conditions. Specifically, it examines the hemodynamic changes that occur with unilateral and bilateral ureteral obstruction, including triphasic patterns of renal blood flow. It also describes the pathologic findings, compensatory renal growth, diagnostic imaging modalities and approaches to relieving obstruction and treating its underlying causes.
Obstructive uropathy refers to any obstruction in the urinary tract. It can cause changes including hydronephrosis (distension of the kidneys and ureters) and hydroureteronephrosis (distension of the kidneys, ureters and bladder). The document discusses the classification, causes, pathology, investigations and management of various types of obstructive uropathy including ureteric strictures and retroperitoneal fibrosis. Surgical intervention is often needed to relieve the obstruction and treat associated complications.
The document summarizes topics related to the renal and urinary system, including benign prostatic hypertrophy (BPH), urinary incontinence, and nephrotic syndrome. It provides details on the pathophysiology, signs and symptoms, diagnostic tests, nursing care, and interventions for BPH. Urinary incontinence is defined and its prevalence among older populations is noted. Various diagnostic tests for incontinence are also listed.
The document provides an overview of renal development and dysplasia. It discusses where renal dysplasia may be encountered, the most common congenital anomalies of the kidney and urinary tract, the stages of renal development, and common anomalies seen including cystic dysplastic kidneys, renal agenesis, horseshoe kidney, and duplicated kidneys and ureters. It also reviews common urogenital anomalies like urinary outlet obstruction and reflux and their causes during renal development.
Ultrasound of the urinary tract - Renal infectionsSamir Haffar
Ultrasound can detect various renal infections including:
1) Acute pyelonephritis seen as renal enlargement, decreased echogenicity, and loss of corticomedullary differentiation on ultrasound.
2) Renal abscesses appear as hypoechoic masses with thick irregular walls that increase in distinctness over time.
3) Pyohydronephrosis is infection of the obstructed collecting system seen as echogenic debris and fluid-fluid levels.
4) Emphysematous pyelonephritis involves gas in the renal parenchyma seen as high amplitude echoes and dirty shadowing.
This document discusses various genitourinary problems seen in pediatric patients. It covers obstructive uropathies like posterior urethral valves and UPJ obstruction. It also discusses genital anomalies such as bladder exstrophy, cloacal exstrophy, ambiguous genitalia, and hypospadias. Additionally, it provides details on cystic kidney diseases, renal tumors, horseshoe kidney and other ectopic kidney anomalies. Imaging approaches and treatment options are presented for many of these conditions.
Hydronephrosis is the dilation of the renal pelvis and calyces caused by obstruction of urine flow from the kidneys. It can cause symptoms ranging from pain to urinary tract infections to kidney damage. Diagnosis involves physical examination, blood tests, urinalysis and imaging like ultrasound or IVU. Treatment depends on the severity and includes drainage of urine through nephrostomy tubes or stents, pyeloplasty to reconstruct the renal pelvis, or suprapubic catheters for lower urinary tract obstruction. Nursing care focuses on monitoring for infections, managing pain and fluids, and educating on symptoms that require medical attention to prevent long term kidney damage from obstruction.
The document provides an overview of the urinary system and disorders that can affect it. It discusses the anatomy and physiology of the kidneys and nephrons. Some key urinary disorders summarized include:
1. Urinary tract infections (UTIs), which are common in women and caused by bacteria entering the urinary tract. Symptoms can include painful urination.
2. Kidney stones, solid mineral deposits that can block the urinary tract. Treatment includes shockwave lithotripsy to break up stones.
3. Benign prostatic hyperplasia (BPH), a non-cancerous enlargement of the prostate common in aging men that causes urinary problems. Treatments include medications
Acute renal failure is a medical emergency characterized by a rapid deterioration of renal function over hours to days. It is often reversible. It accounts for 1% of hospital admissions and complicates around 7% of inpatient episodes, with mortality rates of 5-10% in uncomplicated cases and 50-70% in severe cases involving sepsis or the need for dialysis. Causes include pre-renal factors reducing renal perfusion (40-70% of cases), intrinsic renal disease (10-50% of cases), and post-renal urinary outflow obstruction (10% of cases). Management focuses on treating the underlying cause, monitoring fluid balance, and considering dialysis for uraemic patients. Comp
The ureters are tubular structures that transport urine from the kidneys to the bladder. They have multiple layers including epithelium, smooth muscle, and adventitia. Sites of natural narrowing include the ureteropelvic junction (UPJ) and ureterovesical junction. UPJ obstruction is most common in boys and on the left side. It can be caused by intrinsic narrowing at the UPJ or extrinsic compression. Surgical intervention is considered if renal function declines or symptoms develop. Treatment options include open or laparoscopic pyeloplasty, endopyelotomy, or ureterocalycostomy depending on the specifics of each case.
Hydronephrosis is dilatation of the kidney caused by urine outflow obstruction anywhere along the urinary tract. It can be caused by extramural factors like tumors or retroperitoneal fibrosis, or intramural factors like congenital abnormalities or inflammatory strictures. Bilateral hydronephrosis is commonly due to urethral obstruction from conditions like benign prostatic enlargement. Clinical features depend on severity and location of obstruction, and may include flank pain, urinary symptoms, or renal failure. Diagnosis involves imaging tests like ultrasound and IVU. Treatment involves relieving obstruction through stents, nephrostomy, or open surgery like pyeloplasty depending on severity and cause of obstruction.
1. Antenatal hydronephrosis is a common prenatal finding that requires postnatal evaluation to identify potential kidney abnormalities.
2. Most cases of antenatal hydronephrosis are transient and resolve without intervention, while others may indicate issues like urinary tract obstruction that require treatment.
3. Postnatal evaluation includes ultrasound, voiding cystourethrogram, diuretic renography and other tests to determine the severity and cause of hydronephrosis and assess kidney function.
Constipation is a common gastrointestinal issue in children. It can be functional or organic in nature, with functional constipation making up the majority of cases. The document discusses the definition, epidemiology, risk factors, evaluation, and management of pediatric constipation. Evaluation involves history, physical exam, and potential imaging and testing. Management is multi-pronged, focusing on education, dietary changes, behavioral modifications, disimpaction if needed, and long-term maintenance therapy often involving laxatives. Surgery is rarely needed and reserved for severe, refractory cases. Childhood constipation can sometimes predict irritable bowel syndrome in adulthood.
PUJ obstruction is a restriction of urine flow from the renal pelvis to the ureter. It can be congenital or acquired, with congenital being one of the most common causes of antenatal hydronephrosis. Diagnosis involves ultrasonography, VCUG, diuretic renography and other imaging modalities to determine severity and presence of associated issues. Treatment depends on severity but typically involves surgical intervention like open or laparoscopic pyeloplasty to resect and reanastomose the obstructed segment if drainage is significantly impaired or renal growth is poor. Postoperative follow up with imaging is important to monitor repair.
This document provides an overview of common urologic emergencies and their management. It discusses renal colic caused by kidney stones, including pain management with NSAIDs and opioids. It also covers acute urinary retention, priapism, hematuria, and anuria. For each condition, it outlines evaluation, differential diagnosis, and treatment approaches including medical expulsive therapy, ureteral stenting, and surgical procedures.
Hydronephrosis is the dilation of the renal pelvis and calyces due to partial or intermittent obstruction of urine flow. It is usually caused by blockages or reflux in the urinary tract. Common causes in children include vesicoureteral reflux, ureteropelvic junction obstruction, and posterior urethral valves. Diagnosis involves renal ultrasound and tests to assess kidney function. Treatment depends on the severity and underlying cause, ranging from observation to surgery to correct blockages or reflux. Complications can include urinary tract infections, kidney damage, and renal failure if not properly treated.
PUJO is an obstruction of the proximal ureter at the junction with the renal pelvis. It is most common in childhood, affecting 1 in 1000 children, with boys more commonly affected than girls. Presentation includes flank pain, flank mass, nausea, vomiting, recurrent UTIs, and hematuria. Diagnosis involves blood tests, urine tests, ultrasounds, CT scans, nuclear scans, and retrograde pyelography. Treatment depends on symptoms and impairment - watchful waiting may be sufficient, but surgery like pyeloplasty is often needed and has a high success rate of 90-95%.
Etiopathogenesis, Evaluation & Management of Posterior Urethral ValveShubham Lavania
This document discusses posterior urethral valves (PUV), including their etiology, classification, pathophysiology, clinical presentation, diagnosis, and management. PUV are congenital obstructions of the posterior urethra that commonly cause urinary outflow obstruction in boys. Type I valves are the most common. Initial management involves bladder drainage and antibiotics. Surgical valve ablation is usually curative, but long-term sequelae like renal disease are significant due to the primitive tissue injury caused by the obstruction.
This document summarizes benign prostatic hyperplasia (BPH). It finds that the incidence of BPH increases with age, affecting 20% of men aged 41-50 and over 90% of men over 80. Risk factors include genetics and race. BPH causes both obstructive symptoms like weak urinary stream and irritative symptoms like frequent urination. Treatment options range from watchful waiting for mild cases to drug therapies like alpha blockers and 5-alpha reductase inhibitors to surgical procedures like transurethral resection of the prostate. Minimally invasive procedures also exist like laser therapy, transurethral vaporization of the prostate, and transurethral needle ablation of the prostate.
Most common site of urinary tract obstruction in children
-Majority are discovered antenatal
-1:800-1500 pregnancies
-80% antenatal hydronephrosis
-2:1 boys : girls
-2/3 on the left
-10-40% bilateral
Pelvi ureteric junction obstruction in childrenAseesh Varma
This document discusses pelvi-ureteral junction obstruction (PUJO). It begins by describing fetal urine production and the role of amniotic fluid in lung development. It then covers the causes of PUJO, which can be intrinsic due to abnormal development of the ureteral bud, or extrinsic due to compression from blood vessels. Clinical presentation varies from antenatal detection of hydronephrosis to abdominal pain or urinary tract infections in older children. Diagnosis involves ultrasound to assess renal pelvis dilation and thinning of parenchyma over time.
Pathophysioogy of urinary tract obstruction bassem presentationfreeburn simunchembu
This document discusses obstructive nephropathy and hydronephrosis. It defines key terms and outlines the prevalence, classifications, causes, pathophysiology, diagnosis and management of obstructive kidney conditions. Specifically, it examines the hemodynamic changes that occur with unilateral and bilateral ureteral obstruction, including triphasic patterns of renal blood flow. It also describes the pathologic findings, compensatory renal growth, diagnostic imaging modalities and approaches to relieving obstruction and treating its underlying causes.
Obstructive uropathy refers to any obstruction in the urinary tract. It can cause changes including hydronephrosis (distension of the kidneys and ureters) and hydroureteronephrosis (distension of the kidneys, ureters and bladder). The document discusses the classification, causes, pathology, investigations and management of various types of obstructive uropathy including ureteric strictures and retroperitoneal fibrosis. Surgical intervention is often needed to relieve the obstruction and treat associated complications.
The document summarizes topics related to the renal and urinary system, including benign prostatic hypertrophy (BPH), urinary incontinence, and nephrotic syndrome. It provides details on the pathophysiology, signs and symptoms, diagnostic tests, nursing care, and interventions for BPH. Urinary incontinence is defined and its prevalence among older populations is noted. Various diagnostic tests for incontinence are also listed.
The document provides an overview of renal development and dysplasia. It discusses where renal dysplasia may be encountered, the most common congenital anomalies of the kidney and urinary tract, the stages of renal development, and common anomalies seen including cystic dysplastic kidneys, renal agenesis, horseshoe kidney, and duplicated kidneys and ureters. It also reviews common urogenital anomalies like urinary outlet obstruction and reflux and their causes during renal development.
Ultrasound of the urinary tract - Renal infectionsSamir Haffar
Ultrasound can detect various renal infections including:
1) Acute pyelonephritis seen as renal enlargement, decreased echogenicity, and loss of corticomedullary differentiation on ultrasound.
2) Renal abscesses appear as hypoechoic masses with thick irregular walls that increase in distinctness over time.
3) Pyohydronephrosis is infection of the obstructed collecting system seen as echogenic debris and fluid-fluid levels.
4) Emphysematous pyelonephritis involves gas in the renal parenchyma seen as high amplitude echoes and dirty shadowing.
This document discusses various genitourinary problems seen in pediatric patients. It covers obstructive uropathies like posterior urethral valves and UPJ obstruction. It also discusses genital anomalies such as bladder exstrophy, cloacal exstrophy, ambiguous genitalia, and hypospadias. Additionally, it provides details on cystic kidney diseases, renal tumors, horseshoe kidney and other ectopic kidney anomalies. Imaging approaches and treatment options are presented for many of these conditions.
Hydronephrosis is the dilation of the renal pelvis and calyces caused by obstruction of urine flow from the kidneys. It can cause symptoms ranging from pain to urinary tract infections to kidney damage. Diagnosis involves physical examination, blood tests, urinalysis and imaging like ultrasound or IVU. Treatment depends on the severity and includes drainage of urine through nephrostomy tubes or stents, pyeloplasty to reconstruct the renal pelvis, or suprapubic catheters for lower urinary tract obstruction. Nursing care focuses on monitoring for infections, managing pain and fluids, and educating on symptoms that require medical attention to prevent long term kidney damage from obstruction.
The document provides an overview of the urinary system and disorders that can affect it. It discusses the anatomy and physiology of the kidneys and nephrons. Some key urinary disorders summarized include:
1. Urinary tract infections (UTIs), which are common in women and caused by bacteria entering the urinary tract. Symptoms can include painful urination.
2. Kidney stones, solid mineral deposits that can block the urinary tract. Treatment includes shockwave lithotripsy to break up stones.
3. Benign prostatic hyperplasia (BPH), a non-cancerous enlargement of the prostate common in aging men that causes urinary problems. Treatments include medications
Acute renal failure is a medical emergency characterized by a rapid deterioration of renal function over hours to days. It is often reversible. It accounts for 1% of hospital admissions and complicates around 7% of inpatient episodes, with mortality rates of 5-10% in uncomplicated cases and 50-70% in severe cases involving sepsis or the need for dialysis. Causes include pre-renal factors reducing renal perfusion (40-70% of cases), intrinsic renal disease (10-50% of cases), and post-renal urinary outflow obstruction (10% of cases). Management focuses on treating the underlying cause, monitoring fluid balance, and considering dialysis for uraemic patients. Comp
The ureters are tubular structures that transport urine from the kidneys to the bladder. They have multiple layers including epithelium, smooth muscle, and adventitia. Sites of natural narrowing include the ureteropelvic junction (UPJ) and ureterovesical junction. UPJ obstruction is most common in boys and on the left side. It can be caused by intrinsic narrowing at the UPJ or extrinsic compression. Surgical intervention is considered if renal function declines or symptoms develop. Treatment options include open or laparoscopic pyeloplasty, endopyelotomy, or ureterocalycostomy depending on the specifics of each case.
Hydronephrosis is dilatation of the kidney caused by urine outflow obstruction anywhere along the urinary tract. It can be caused by extramural factors like tumors or retroperitoneal fibrosis, or intramural factors like congenital abnormalities or inflammatory strictures. Bilateral hydronephrosis is commonly due to urethral obstruction from conditions like benign prostatic enlargement. Clinical features depend on severity and location of obstruction, and may include flank pain, urinary symptoms, or renal failure. Diagnosis involves imaging tests like ultrasound and IVU. Treatment involves relieving obstruction through stents, nephrostomy, or open surgery like pyeloplasty depending on severity and cause of obstruction.
1. Antenatal hydronephrosis is a common prenatal finding that requires postnatal evaluation to identify potential kidney abnormalities.
2. Most cases of antenatal hydronephrosis are transient and resolve without intervention, while others may indicate issues like urinary tract obstruction that require treatment.
3. Postnatal evaluation includes ultrasound, voiding cystourethrogram, diuretic renography and other tests to determine the severity and cause of hydronephrosis and assess kidney function.
Similar to Pelvi-ureteric junction obstruction (20)
Constipation is a common gastrointestinal issue in children. It can be functional or organic in nature, with functional constipation making up the majority of cases. The document discusses the definition, epidemiology, risk factors, evaluation, and management of pediatric constipation. Evaluation involves history, physical exam, and potential imaging and testing. Management is multi-pronged, focusing on education, dietary changes, behavioral modifications, disimpaction if needed, and long-term maintenance therapy often involving laxatives. Surgery is rarely needed and reserved for severe, refractory cases. Childhood constipation can sometimes predict irritable bowel syndrome in adulthood.
This document discusses intussusception, which is the invagination of one part of the intestine into another. It is most common in infants and toddlers, with 90% occurring in children within 3 years of age. There are different types including general, specific, anatomic. Treatment involves admission, hydration, antibiotics, and intervention such as intussusception reduction through open surgery, USG guided hydrostatic reduction, or C-arm guided pneumatic reduction. C-arm guided pneumatic reduction has benefits such as being quick, ensuring procedure completion under anesthesia with less risk of complications compared to other methods. Exploration surgery may be needed if reduction fails or there are issues like bowel gangrene or perforation.
This document provides an overview of anorectal malformations (ARM), including their definition, embryology, clinical presentation, associated anomalies, evaluation, classification, and management protocols. It describes in detail:
- The embryological causes of ARM and common associated genetic syndromes.
- Methods for antenatal diagnosis using ultrasound and MRI.
- How to examine males and females with ARM to determine the type and severity.
- Classification systems for ARM including the Krickenbeck system.
- Evaluation protocols including imaging, bloodwork, and physical exams.
- Initial management algorithms including colostomy placement.
- Surgical repair techniques for different ARM types like PSARP and approaches for complex cases like cloaca
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.
Adhd Medication Shortage Uk - trinexpharmacy.comreignlana06
The UK is currently facing a Adhd Medication Shortage Uk, which has left many patients and their families grappling with uncertainty and frustration. ADHD, or Attention Deficit Hyperactivity Disorder, is a chronic condition that requires consistent medication to manage effectively. This shortage has highlighted the critical role these medications play in the daily lives of those affected by ADHD. Contact : +1 (747) 209 – 3649 E-mail : sales@trinexpharmacy.com
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
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.
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by...Donc Test
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by Stamler, Verified Chapters 1 - 33, Complete Newest Version Community Health Nursing A Canadian Perspective, 5th Edition by Stamler, Verified Chapters 1 - 33, Complete Newest Version Community Health Nursing A Canadian Perspective, 5th Edition by Stamler Community Health Nursing A Canadian Perspective, 5th Edition TEST BANK by Stamler Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Pdf Chapters Download Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Pdf Download Stuvia Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Study Guide Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Ebook Download Stuvia Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Questions and Answers Quizlet Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Studocu Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Quizlet Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Pdf Chapters Download Community Health Nursing A Canadian Perspective, 5th Edition Pdf Download Course Hero Community Health Nursing A Canadian Perspective, 5th Edition Answers Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Ebook Download Course hero Community Health Nursing A Canadian Perspective, 5th Edition Questions and Answers Community Health Nursing A Canadian Perspective, 5th Edition Studocu Community Health Nursing A Canadian Perspective, 5th Edition Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Pdf Chapters Download Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Pdf Download Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Study Guide Questions and Answers Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Ebook Download Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Questions Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Studocu Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Stuvia
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
- 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
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
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.
9. Introduction
Incidence - 1 in 1250 live births
M:F=2:1
PUJO- Adynamic segment
High grade vs Low grade
Intrinsic Vs Extrinsic
10.
11. Etiology
Primary PUJO:
Intrinsic obstruction – Scarring of ureteric
valves
Ureteral hypoplasia- Inhibit the natural
peristaltic emptying
Abnormal or high insertion of the ureter
Crossing lower-pole renal vessel(s)
Renal ectopy
Renal Hypermobility
Secondary PUJO: Renal stone disease,
Failed repair,
12. Pathophysiology
Adynamic segment in upper ureter,
Obstructing lesions(Valves, Polyps)
Folds(Persistent Ostlings folds).
Complete obstruction- Rapid deterioration
of function
Partial obstruction- Gradual deterioration
of function
13. Clinical Presentation
Increasing prenatal
detection- 80%
Asymtomatic PUJO in infants
Abdominal lump
Abdominal pain
Urinary tract infection
Dietl’s crisis
Hematuria, Hypertension
Association with other
anomalies- Anorectal,
syndromes-MRKH
18. Diuretic Renogram
Replaced IVP – negligible radiation
Sensitivity 100% and Specificity 94%
Objective assessment:
Renal blood flow
Differential renal function
Intra renal transit time
Time taken for radioisotope washout from
the pelvicalyceal system (t½)
Follow-up and postoperative assessment
19.
20. Diuretic Renogram
The “Well – Tempered”
renogram – standard
practice and comparable
results
Hydration
Bladder catheter
Furosemide injection
– F0/F15 protocol
First Renogram
EC - 4 Wks of Age
MAG3- 15 days
21. Magnetic Resonance Urography
•MR renography (Gd – DTPA)
Anatomic and functional
assessment
•Selective usage- anatomical
anomalies- Duplex, ectopia,
malrotation
22. Indications for Pyeloplasty
Differential renal function below
40%
Decrease in DRF > 5% on subsequent
renal scintigraphy scan
T ½ max - >20 min
Recurrent urinary tract infections
Rapid aggravation of hydronephrosis
Severe bilateral hydronephrosis due
to PUJO
23. Indications for Pyeloplasty
•DOCUMENTED OBSTRUCTION on
nuclear imaging irrespective of
DRF and grade of hydronephrosis
•Equivocal - regular and close follow
up
25. Intubated pyeloplasty
•Long segments of
narrowing of ureter
•Contraindicated in
aberrant lower polar
artery
•Higher fibrosis and
restenosis rates
•Long term success rates -
50 – 88 %
26. Flap Repairs
•Pelvic flaps without sacrificing ureteropelvic
continuity- for Small extra renal pelvis
Foley Y – V plasty
Culp – DeWeerd spiral flap
Scardinho – Prince vertical flap
• Rarely performed and have specific indications
27. Dismembered pyeloplasty
Modified Anderson Hynes Pyeloplasty
for PUJ obstruction
Excision of redundant pelvis
Excision of pathological PUJ segment
Spatulated wide ureteropelvic anastomosis
Dependent
Water tight
Tension free anastomosis
36. PUJ and polar vessels
•Often a surprise
•Rarely associated
with intrinsic PUJ
obstruction
•Pyelopyelostomy
•A-H Pyeloplasty
37. PUJ and VUJ obstruction
•The saline flush test for distal patency
•Missed VUJ obstruction – large low pelvis
•DJ stent / nephrostomy till VUJ is addressed
(Ureteric reimplantation )
38. PUJ obstruction and VUR
•10% PUJO – concurrent reflux
•Routine MCU
Bilateral HDN
Ureteric dilatation on preop USG
• Dilated ureter at operation
• Pyeloplasty - post op MCU / DMSA
• Manage VUR on merits