Why do we make kidney stones, how are they evaluated and how are they prevented?
Dr. Britton E. Tisdale, MD, Urologist, UBMD Urology
Buffalo Niagara / Western New York Area
There are many different types of kidney cysts that can be classified in various ways. An ideal classification system would take into account morphological features, pathogenesis, and therapeutic potential. Autosomal dominant polycystic kidney disease (ADPKD) is the most common cystic kidney disease and is characterized by multiple bilateral cysts of varying sizes in the kidneys and liver. It has a prevalence of 1 in 400 to 1,000 people and is caused by mutations in the PKD1 or PKD2 genes.
Cystic liver lesions - An ultrasound perspectiveSamir Haffar
This document summarizes the diagnosis and imaging findings of various cystic hepatic lesions. It describes simple hepatic cysts, hydatid cysts, and congenital fibrocystic liver diseases including biliary hamartomas, peribiliary cysts, choledochal cysts, and polycystic liver disease. Imaging findings on ultrasound, CT, MRI, and MRCP are provided for each condition to aid diagnosis. Differential features between lesion types are emphasized, along with WHO classification of hydatid cyst appearance and post-operative evaluation of hydatid cyst treatment.
Congenital anamalies of biliary system aryajaRamesh Bhat
This document discusses various congenital anomalies of the biliary system. It describes abnormalities that can occur in the gallbladder, hepatic ducts, cystic duct, arteries, and other structures. Some key points include:
- The gallbladder may be absent, duplicated, located on the left side, or intrahepatic.
- Accessory hepatic ducts occur in around 15% of cases.
- Variations can occur in the origins of the cystic and hepatic arteries.
- The cystic duct can drain into various locations and have other anomalies.
- Choledochal cysts are cystic dilations that can affect different parts of the biliary tree.
- Congenital biliary at
it is uploaded to create awareness about congenital abnormality of urinary system. it also help nursing & paramedics educators to teach their students about it.
This document provides information on portal hypertension and its surgical management. It begins with the history of portal hypertension, describing early anatomists who studied the portal venous system. It then covers the anatomy of the portal system and pathophysiology of portal hypertension. Etiologies of portal hypertension including pre-hepatic, hepatic, and post-hepatic causes are discussed. Clinical presentation, diagnosis, evaluation, and general management approaches are summarized. The document concludes by focusing on surgical options for treating portal hypertension including devascularization procedures and liver transplantation.
Gallbladder disease is common, affecting around 5% of the population. Gallstones are the most common cause of gallbladder disease and occur more often in women, with increasing age. Symptoms include biliary colic, acute cholecystitis, and in rare cases gallbladder cancer. Treatment options include oral medication, lithotripsy for single stones, and cholecystectomy for symptomatic or complicated cases. Complications can include cholangitis, pancreatitis, and choledocholithiasis requiring ERCP.
This document contains information about a patient visit. A 42-year-old real estate agent named Fay approached the assistant at a charity function with abdominal problems and was advised to see the assistant at their surgery. The document then provides detailed information about Fay's medical history, symptoms, lab results, and differential diagnoses. It discusses conditions like gallstones, cholecystitis, liver disease, and more.
There are many different types of kidney cysts that can be classified in various ways. An ideal classification system would take into account morphological features, pathogenesis, and therapeutic potential. Autosomal dominant polycystic kidney disease (ADPKD) is the most common cystic kidney disease and is characterized by multiple bilateral cysts of varying sizes in the kidneys and liver. It has a prevalence of 1 in 400 to 1,000 people and is caused by mutations in the PKD1 or PKD2 genes.
Cystic liver lesions - An ultrasound perspectiveSamir Haffar
This document summarizes the diagnosis and imaging findings of various cystic hepatic lesions. It describes simple hepatic cysts, hydatid cysts, and congenital fibrocystic liver diseases including biliary hamartomas, peribiliary cysts, choledochal cysts, and polycystic liver disease. Imaging findings on ultrasound, CT, MRI, and MRCP are provided for each condition to aid diagnosis. Differential features between lesion types are emphasized, along with WHO classification of hydatid cyst appearance and post-operative evaluation of hydatid cyst treatment.
Congenital anamalies of biliary system aryajaRamesh Bhat
This document discusses various congenital anomalies of the biliary system. It describes abnormalities that can occur in the gallbladder, hepatic ducts, cystic duct, arteries, and other structures. Some key points include:
- The gallbladder may be absent, duplicated, located on the left side, or intrahepatic.
- Accessory hepatic ducts occur in around 15% of cases.
- Variations can occur in the origins of the cystic and hepatic arteries.
- The cystic duct can drain into various locations and have other anomalies.
- Choledochal cysts are cystic dilations that can affect different parts of the biliary tree.
- Congenital biliary at
it is uploaded to create awareness about congenital abnormality of urinary system. it also help nursing & paramedics educators to teach their students about it.
This document provides information on portal hypertension and its surgical management. It begins with the history of portal hypertension, describing early anatomists who studied the portal venous system. It then covers the anatomy of the portal system and pathophysiology of portal hypertension. Etiologies of portal hypertension including pre-hepatic, hepatic, and post-hepatic causes are discussed. Clinical presentation, diagnosis, evaluation, and general management approaches are summarized. The document concludes by focusing on surgical options for treating portal hypertension including devascularization procedures and liver transplantation.
Gallbladder disease is common, affecting around 5% of the population. Gallstones are the most common cause of gallbladder disease and occur more often in women, with increasing age. Symptoms include biliary colic, acute cholecystitis, and in rare cases gallbladder cancer. Treatment options include oral medication, lithotripsy for single stones, and cholecystectomy for symptomatic or complicated cases. Complications can include cholangitis, pancreatitis, and choledocholithiasis requiring ERCP.
This document contains information about a patient visit. A 42-year-old real estate agent named Fay approached the assistant at a charity function with abdominal problems and was advised to see the assistant at their surgery. The document then provides detailed information about Fay's medical history, symptoms, lab results, and differential diagnoses. It discusses conditions like gallstones, cholecystitis, liver disease, and more.
This document summarizes the anatomy, histology, common abnormalities and disorders of the esophagus. It discusses congenital anomalies like tracheoesophageal fistulas. It also covers acquired conditions such as esophageal diverticula, motor disorders like achalasia, inflammatory disorders including different types of esophagitis, Barrett's esophagus and esophageal cancer. Esophageal adenocarcinoma arises from Barrett's esophagus while squamous cell carcinoma is more common in other parts of the esophagus. Both types usually present at late stages with poor prognosis.
This presentation comprises of congenital anomalies of kidney and urinary tract made concise and in depth for PG preparation. It contains all important topics of the regarding subject covered in detail.
Portal hypertension is caused by increased vascular resistance and blood flow and can result from cirrhosis, vascular diseases, or other conditions. It leads to complications like ascites, variceal bleeding, and hepatic encephalopathy. Treatment involves general measures, variceal treatment including banding, TIPS procedure, and in some cases transplantation. Ascites is treated with paracentesis and diuretics along with albumin to prevent renal failure.
- Normal portal venous pressure is generally considered to be between 5-10 mm Hg. Once it rises to 12 mm Hg or greater, complications can arise such as varices and ascites.
- Portal hypertension is defined as an elevation of the hepatic venous pressure gradient to over 5 mmHg. This gradient is the difference between the wedged hepatic venous pressure (sinusoidal pressure) and the free hepatic venous pressure.
- The two main types of portal hypertension are sinusoidal, where the sinusoidal pressure is elevated, and presinusoidal, where the portal venous pressure is increased but the sinusoidal pressure is normal. Sinusoidal hypertension commonly results in ascites due to increased transudation of fluid from the sin
Acute cholangitis is an infection of the bile ducts caused by obstruction and bacterial overgrowth. It presents with fever, jaundice, and right upper quadrant pain (Charcot's triad). Obstruction leads to increased pressure and bacterial growth in the bile ducts. Diagnosis involves blood tests, imaging like ultrasound or CT, and testing bile if drained. Treatment is antibiotics, hydration, and relieving obstruction endoscopically or surgically. Antibiotics are continued until obstruction is fully resolved to prevent recurrence.
This document provides an overview of common congenital anomalies of the genitourinary system. It discusses abnormalities of the kidneys, ureters, bladder, urethra, and genitals. For each anomaly, it describes the presentation, evaluation, and typical treatment approaches. Common anomalies covered include horseshoe kidney, pelviureteric junction obstruction, vesicoureteric reflux, duplication of the urinary system, ectopic ureter, uretrocele, undescended testis, hypospadias, epispadias, bladder extrophy, and posterior urethral valves.
- Autosomal dominant polycystic kidney disease (ADPKD) is characterized by multiple bilateral renal cysts that lead to kidney enlargement and failure. It has a prevalence of 1 in 400 to 1000 live births.
- The disease is caused by mutations in the PKD1 and PKD2 genes which code for polycystin proteins 1 and 2. These proteins are involved in cellular signaling pathways regulating cell proliferation and adhesion. Loss of function of these proteins results in focal cyst formation in the kidneys.
- Current treatments aim to slow cyst growth and decline in kidney function. Vasopressin receptor antagonists like tolvaptan have shown some efficacy in reducing total kidney volume increase in
This document provides information on differential diagnosis and evaluation of abdominal pain localized to the epigastric region. It discusses obtaining a thorough history and performing physical exam, lab tests, imaging studies, and endoscopy to diagnose potential causes such as biliary diseases, gastrointestinal issues, cardiac problems, vascular issues, and others. Key details on symptoms, diagnostic criteria, and evaluation of specific conditions like cholecystitis, pancreatitis, peptic ulcer disease, and mesenteric ischemia are also provided.
Doppler ultrasound of the liver in hereditary hemorrhagic telangiectasiaSamir Haffar
This document discusses Doppler ultrasound findings in hereditary hemorrhagic telangiectasia (HHT). HHT is characterized by epistaxis, telangiectases, and vascular malformations. Doppler ultrasound can detect hepatic involvement in HHT, including dilated and tortuous hepatic arteries, arterio-portal shunts, and arterio-systemic shunts. The document outlines diagnostic criteria for HHT and provides examples of ultrasound images demonstrating various vascular abnormalities that can occur in the liver as a result of the condition.
This document provides definitions and overview of various cystic kidney diseases including simple cysts, autosomal dominant polycystic kidney disease (ADPKD), autosomal recessive polycystic kidney disease (ARPKD), acquired cystic kidney disease, Alport's syndrome, medullary sponge kidney, medullary cystic kidney disease, and renal phacomatosis associated with tuberous sclerosis and Von Hippel-Lindau disease. It describes the clinical features, pathogenesis, diagnosis, and management of these conditions.
The document provides information on the normal anatomy and histology of the pancreas. It notes that the pancreas has both exocrine and endocrine functions, is retroperitoneal in location, and drains into the duodenum via the pancreatic duct system. The endocrine portion is composed of islets of Langerhans that secrete insulin, glucagon, and somatostatin. Common congenital anomalies and acquired conditions of the pancreas are also described.
This document provides information about carcinoma of the esophagus, including its epidemiology, risk factors, pathological classification, clinical features, investigations, diagnosis and staging, and treatment. Carcinoma of the esophagus is most common in China, South Africa, and parts of India. It typically presents with dysphagia. Investigations include endoscopy with biopsy, imaging like CT and PET scans, and endoscopic ultrasound. Treatment depends on the stage, with surgery or chemoradiation used for early-stage or locally advanced carcinoma, and palliative approaches for metastatic disease.
1. Ascites is an accumulation of fluid in the peritoneal cavity, most commonly caused by cirrhosis of the liver.
2. Diagnosis involves physical exam findings, ultrasound imaging, and analysis of ascitic fluid. A serum ascites albumin gradient (SAAG) can help determine if ascites is caused by portal hypertension.
3. Initial treatment involves sodium restriction, diuretics like spironolactone and furosemide, and therapeutic paracentesis if needed. Refractory ascites may require transjugular intrahepatic portosystemic shunt or liver transplantation.
This document provides an overview of various renal infectious and inflammatory diseases. It begins by outlining pyelonephritis, including predisposing factors, clinical presentation, imaging findings on ultrasound, CT, and pathology. Complications of pyelonephritis such as abscesses, emphysematous pyelonephritis, and pyonephrosis are then reviewed. The document concludes by discussing other infectious conditions including tuberculosis, xanthogranulomatous pyelonephritis, renal malakoplakia, and fungal disease. Imaging findings and characteristics of each condition are emphasized.
Hepatic cysts are abnormal fluid-filled spaces in the hepatic parenchyma and biliary tree
They are categorized into 3 main types:
fibrocystic diseases of the liver
cystadenomas and cystadenocarcinomas
and hydatid cysts
This document discusses acute pancreatitis, including its etiology, pathogenesis, clinical manifestations, diagnosis, and treatment. It defines acute pancreatitis as inflammation of the pancreas induced by the activation of pancreatic enzymes from various causes. The main causes are biliary diseases, alcohol use, hyperlipidemia, and certain drugs. Clinical features include abdominal pain, nausea, vomiting, and fever. Diagnosis is based on symptoms, elevated serum amylase, and imaging findings. Treatment differs between mild and severe acute pancreatitis and focuses on supportive care, pain management, inhibiting pancreatic enzymes, preventing infections and organ failure.
Polycystic disease of the kidney (PKD) is a disorder in which major portion of the renal parenchyma is converted into cysts of varying size .
Fluid-filled cysts distributed over the kidney results in massive enlargement of the kidneys.
This document discusses perinephric abscesses. It defines the perinephric space as the area surrounding the kidney that contains fat, vessels and lymphatics. A perinephric abscess can result from a ruptured renal abscess, direct spread from pyelonephritis, or other inflammatory processes outside Gerota's fascia. Ultrasound and CT are used to identify fluid or soft tissue in the perinephric space. Percutaneous drainage under imaging guidance and antibiotics is the primary treatment, with surgery reserved for cases that do not respond to drainage and medication.
Hydronephrosis is the dilation of the renal pelvis and calyces caused by obstruction of urine flow from the kidney. It can be caused by issues in the ureter, bladder, or urethra that limit urine outflow. Unilateral hydronephrosis may cause dull flank pain while bilateral obstruction can lead to decreased urine output. Left untreated, hydronephrosis can damage kidney tissue and impair renal function. Diagnosis is made through imaging tests like intravenous pyelogram. Treatment focuses on resolving the underlying cause of obstruction.
Kidney stones form when dietary minerals in urine become concentrated enough to crystallize. They are typically classified by location and chemical composition, with calcium salts and uric acid being most common. Risk factors include diet, medical conditions, and family history. Stones form through supersaturation when urine is too concentrated for minerals to remain in solution. Symptoms include flank pain, nausea, and blood in urine. Diagnosis involves history, physical exam, and imaging tests like ultrasound or CT. Treatment focuses on resolving underlying causes and preventing stone recurrence.
This document discusses renal calculi (kidney stones). It defines renal calculi and reviews the anatomy and physiology of the renal system. It examines the etiology, risk factors, and pathogenesis of renal calculi. It also describes the clinical manifestations, diagnostic studies, medical and surgical management, nursing management including nursing diagnoses, and prevention of renal calculi.
This document summarizes the anatomy, histology, common abnormalities and disorders of the esophagus. It discusses congenital anomalies like tracheoesophageal fistulas. It also covers acquired conditions such as esophageal diverticula, motor disorders like achalasia, inflammatory disorders including different types of esophagitis, Barrett's esophagus and esophageal cancer. Esophageal adenocarcinoma arises from Barrett's esophagus while squamous cell carcinoma is more common in other parts of the esophagus. Both types usually present at late stages with poor prognosis.
This presentation comprises of congenital anomalies of kidney and urinary tract made concise and in depth for PG preparation. It contains all important topics of the regarding subject covered in detail.
Portal hypertension is caused by increased vascular resistance and blood flow and can result from cirrhosis, vascular diseases, or other conditions. It leads to complications like ascites, variceal bleeding, and hepatic encephalopathy. Treatment involves general measures, variceal treatment including banding, TIPS procedure, and in some cases transplantation. Ascites is treated with paracentesis and diuretics along with albumin to prevent renal failure.
- Normal portal venous pressure is generally considered to be between 5-10 mm Hg. Once it rises to 12 mm Hg or greater, complications can arise such as varices and ascites.
- Portal hypertension is defined as an elevation of the hepatic venous pressure gradient to over 5 mmHg. This gradient is the difference between the wedged hepatic venous pressure (sinusoidal pressure) and the free hepatic venous pressure.
- The two main types of portal hypertension are sinusoidal, where the sinusoidal pressure is elevated, and presinusoidal, where the portal venous pressure is increased but the sinusoidal pressure is normal. Sinusoidal hypertension commonly results in ascites due to increased transudation of fluid from the sin
Acute cholangitis is an infection of the bile ducts caused by obstruction and bacterial overgrowth. It presents with fever, jaundice, and right upper quadrant pain (Charcot's triad). Obstruction leads to increased pressure and bacterial growth in the bile ducts. Diagnosis involves blood tests, imaging like ultrasound or CT, and testing bile if drained. Treatment is antibiotics, hydration, and relieving obstruction endoscopically or surgically. Antibiotics are continued until obstruction is fully resolved to prevent recurrence.
This document provides an overview of common congenital anomalies of the genitourinary system. It discusses abnormalities of the kidneys, ureters, bladder, urethra, and genitals. For each anomaly, it describes the presentation, evaluation, and typical treatment approaches. Common anomalies covered include horseshoe kidney, pelviureteric junction obstruction, vesicoureteric reflux, duplication of the urinary system, ectopic ureter, uretrocele, undescended testis, hypospadias, epispadias, bladder extrophy, and posterior urethral valves.
- Autosomal dominant polycystic kidney disease (ADPKD) is characterized by multiple bilateral renal cysts that lead to kidney enlargement and failure. It has a prevalence of 1 in 400 to 1000 live births.
- The disease is caused by mutations in the PKD1 and PKD2 genes which code for polycystin proteins 1 and 2. These proteins are involved in cellular signaling pathways regulating cell proliferation and adhesion. Loss of function of these proteins results in focal cyst formation in the kidneys.
- Current treatments aim to slow cyst growth and decline in kidney function. Vasopressin receptor antagonists like tolvaptan have shown some efficacy in reducing total kidney volume increase in
This document provides information on differential diagnosis and evaluation of abdominal pain localized to the epigastric region. It discusses obtaining a thorough history and performing physical exam, lab tests, imaging studies, and endoscopy to diagnose potential causes such as biliary diseases, gastrointestinal issues, cardiac problems, vascular issues, and others. Key details on symptoms, diagnostic criteria, and evaluation of specific conditions like cholecystitis, pancreatitis, peptic ulcer disease, and mesenteric ischemia are also provided.
Doppler ultrasound of the liver in hereditary hemorrhagic telangiectasiaSamir Haffar
This document discusses Doppler ultrasound findings in hereditary hemorrhagic telangiectasia (HHT). HHT is characterized by epistaxis, telangiectases, and vascular malformations. Doppler ultrasound can detect hepatic involvement in HHT, including dilated and tortuous hepatic arteries, arterio-portal shunts, and arterio-systemic shunts. The document outlines diagnostic criteria for HHT and provides examples of ultrasound images demonstrating various vascular abnormalities that can occur in the liver as a result of the condition.
This document provides definitions and overview of various cystic kidney diseases including simple cysts, autosomal dominant polycystic kidney disease (ADPKD), autosomal recessive polycystic kidney disease (ARPKD), acquired cystic kidney disease, Alport's syndrome, medullary sponge kidney, medullary cystic kidney disease, and renal phacomatosis associated with tuberous sclerosis and Von Hippel-Lindau disease. It describes the clinical features, pathogenesis, diagnosis, and management of these conditions.
The document provides information on the normal anatomy and histology of the pancreas. It notes that the pancreas has both exocrine and endocrine functions, is retroperitoneal in location, and drains into the duodenum via the pancreatic duct system. The endocrine portion is composed of islets of Langerhans that secrete insulin, glucagon, and somatostatin. Common congenital anomalies and acquired conditions of the pancreas are also described.
This document provides information about carcinoma of the esophagus, including its epidemiology, risk factors, pathological classification, clinical features, investigations, diagnosis and staging, and treatment. Carcinoma of the esophagus is most common in China, South Africa, and parts of India. It typically presents with dysphagia. Investigations include endoscopy with biopsy, imaging like CT and PET scans, and endoscopic ultrasound. Treatment depends on the stage, with surgery or chemoradiation used for early-stage or locally advanced carcinoma, and palliative approaches for metastatic disease.
1. Ascites is an accumulation of fluid in the peritoneal cavity, most commonly caused by cirrhosis of the liver.
2. Diagnosis involves physical exam findings, ultrasound imaging, and analysis of ascitic fluid. A serum ascites albumin gradient (SAAG) can help determine if ascites is caused by portal hypertension.
3. Initial treatment involves sodium restriction, diuretics like spironolactone and furosemide, and therapeutic paracentesis if needed. Refractory ascites may require transjugular intrahepatic portosystemic shunt or liver transplantation.
This document provides an overview of various renal infectious and inflammatory diseases. It begins by outlining pyelonephritis, including predisposing factors, clinical presentation, imaging findings on ultrasound, CT, and pathology. Complications of pyelonephritis such as abscesses, emphysematous pyelonephritis, and pyonephrosis are then reviewed. The document concludes by discussing other infectious conditions including tuberculosis, xanthogranulomatous pyelonephritis, renal malakoplakia, and fungal disease. Imaging findings and characteristics of each condition are emphasized.
Hepatic cysts are abnormal fluid-filled spaces in the hepatic parenchyma and biliary tree
They are categorized into 3 main types:
fibrocystic diseases of the liver
cystadenomas and cystadenocarcinomas
and hydatid cysts
This document discusses acute pancreatitis, including its etiology, pathogenesis, clinical manifestations, diagnosis, and treatment. It defines acute pancreatitis as inflammation of the pancreas induced by the activation of pancreatic enzymes from various causes. The main causes are biliary diseases, alcohol use, hyperlipidemia, and certain drugs. Clinical features include abdominal pain, nausea, vomiting, and fever. Diagnosis is based on symptoms, elevated serum amylase, and imaging findings. Treatment differs between mild and severe acute pancreatitis and focuses on supportive care, pain management, inhibiting pancreatic enzymes, preventing infections and organ failure.
Polycystic disease of the kidney (PKD) is a disorder in which major portion of the renal parenchyma is converted into cysts of varying size .
Fluid-filled cysts distributed over the kidney results in massive enlargement of the kidneys.
This document discusses perinephric abscesses. It defines the perinephric space as the area surrounding the kidney that contains fat, vessels and lymphatics. A perinephric abscess can result from a ruptured renal abscess, direct spread from pyelonephritis, or other inflammatory processes outside Gerota's fascia. Ultrasound and CT are used to identify fluid or soft tissue in the perinephric space. Percutaneous drainage under imaging guidance and antibiotics is the primary treatment, with surgery reserved for cases that do not respond to drainage and medication.
Hydronephrosis is the dilation of the renal pelvis and calyces caused by obstruction of urine flow from the kidney. It can be caused by issues in the ureter, bladder, or urethra that limit urine outflow. Unilateral hydronephrosis may cause dull flank pain while bilateral obstruction can lead to decreased urine output. Left untreated, hydronephrosis can damage kidney tissue and impair renal function. Diagnosis is made through imaging tests like intravenous pyelogram. Treatment focuses on resolving the underlying cause of obstruction.
Kidney stones form when dietary minerals in urine become concentrated enough to crystallize. They are typically classified by location and chemical composition, with calcium salts and uric acid being most common. Risk factors include diet, medical conditions, and family history. Stones form through supersaturation when urine is too concentrated for minerals to remain in solution. Symptoms include flank pain, nausea, and blood in urine. Diagnosis involves history, physical exam, and imaging tests like ultrasound or CT. Treatment focuses on resolving underlying causes and preventing stone recurrence.
This document discusses renal calculi (kidney stones). It defines renal calculi and reviews the anatomy and physiology of the renal system. It examines the etiology, risk factors, and pathogenesis of renal calculi. It also describes the clinical manifestations, diagnostic studies, medical and surgical management, nursing management including nursing diagnoses, and prevention of renal calculi.
This presentation provides an overview of kidney stones, including their incidence, types, causes, symptoms, diagnosis, and treatment. Kidney stones, also called renal calculi, form when substances in urine crystallize and harden. The most common types are calcium and uric acid stones. Risk factors include dehydration and family history. Symptoms include flank pain and blood in the urine. Diagnosis involves tests of urine and imaging of the kidneys. Treatment focuses on pain relief, increasing fluid intake, and sometimes surgical procedures to break up or remove stones.
The document describes the anatomy and physiology of the urinary tract and kidney, risk factors and types of kidney stones, and methods for diagnosing and treating stones, including increasing fluid intake, altering diet, using medications to change urine composition, and surgically removing stones with procedures like ureteroscopy and lithotripsy. Kidney stones form when substances like calcium, oxalate, and uric acid become supersaturated in the urine and crystallize into solid masses.
ROLE OF PHARMACIST IN MANAGEMENT OF KIDNEY STONES FROM RECURRENT UTINikhila Yaladanda
This document discusses the role of pharmacists in managing recurrent urinary tract infections (UTIs) that can lead to kidney stones. It outlines the causes, risk factors, and types of kidney stones. It then presents a case study of a 20-year-old female patient who experienced recurring UTIs and developed a kidney stone due to lack of pharmacist counseling on medication adherence and lifestyle changes. The document emphasizes the importance of pharmacist education to prevent reoccurrence of UTIs and kidney stones through non-pharmacological measures like diet, exercise and ensuring patients understand appropriate medication use.
This document discusses kidney stones, also known as renal calculi. It covers the main types of kidney stones including calcium salts, uric acid, magnesium ammonium phosphate, and cystine stones. It describes the conditions that can cause stone formation such as high concentrations of stone-forming metabolites in the urine, changes in urine pH, urinary stagnation, and deficiencies of stone-inhibiting substances. Laboratory investigations of stones and urine are important to identify the type of stone and underlying causes in order to guide prevention and treatment.
This document discusses urolithiasis (kidney stones). It begins by defining urolithiasis and noting its prevalence and cost. It then covers the epidemiology, types, symptoms, diagnosis, and management of kidney stones. The main points are that kidney stones can form anywhere in the urinary tract, have a lifetime risk of 2-20% depending on location, and are most commonly treated through active medical expulsion or minimally invasive surgeries like ESWL or ureteroscopy. Surgical intervention is indicated for large or obstructing stones, infection, or if conservative measures fail.
This document discusses long-term use of proton pump inhibitors (PPIs) and potential risks and conditions for use. It notes that long-term PPI use has been associated with chronic kidney disease (CKD) and dementia, though the relationships are uncertain. For conditions like GERD, NSAID use, and Barrett's esophagus, the benefits of PPIs usually outweigh the small and uncertain risks. The document provides guidance on what to tell patients about risk/benefit assessments and recommends the lowest effective dose and intermittent use when possible to reduce potential side effects.
This document summarizes the formation and types of kidney stones (urolithiasis). Stones have two parts - a matrix and crystalline components. The matrix acts as a scaffold for microcrystals to deposit on. Crystals form via nucleation, growth, and aggregation. Stone formation can be influenced by ions like calcium, oxalate, phosphates, and citrate, as well as proteins and trace metals. Various metabolic conditions can lead to hypercalciuria, hyperoxaluria, hyperuricosuria, and hypocitraturia, promoting stone risk. Specific types of stones include calcium, uric acid, struvite, cystine, and others. Testing and treatments aim to identify the underlying metabolic
There are four main types of kidney stones: calcium, uric acid, struvite, and cystine. Calcium stones are the most common, forming when there are high levels of calcium or oxalate in the urine. Uric acid stones form when urine is acidic. Struvite stones often form due to urinary tract infections, and can grow quite large. Cystine stones occur in people with a rare genetic disorder. Kidney stones are diagnosed through physical exams, blood and urine tests, and imaging tests like ultrasound or CT scans. Treatment involves increasing fluid intake, using medication to prevent stone formation, or surgical procedures like ESWL to break up stones.
Foods to Eat in Kidney Stones in Hindi Iकिडनी स्टोन में क्या खाएIHerbal Daily
This document provides dietary and lifestyle recommendations for preventing and treating kidney stones. It recommends drinking plenty of fluids, especially water, to dilute urine and flush out toxins. It also suggests consuming foods high in magnesium, potassium, and citrus fruits/juices to alkalize the body and prevent stone formation, while limiting salt and animal proteins. Several herbs and home remedies using foods like lemon, olive oil, and apple cider vinegar are also listed to help dissolve existing stones.
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder characterized by multiple bilateral renal cysts that can lead to kidney failure, with mutations in two genes causing cyst formation through disordered polycystin function; it commonly causes hypertension, pain, infection, and kidney failure and can involve the liver and other organs; management focuses on slowing progression through blood pressure control, pain management, and potentially targeting the renin-angiotensin system or mTOR pathway.
The document discusses polycystic kidney disease (PKD), which is an inherited disorder characterized by the growth of numerous cysts in the kidneys. There are three main types of PKD - autosomal dominant PKD, autosomal recessive PKD, and acquired cystic kidney disease. Autosomal dominant PKD is the most common, accounting for 90% of cases and caused by mutations in the PKD1 or PKD2 genes. Autosomal recessive PKD is rare and caused by mutations in the PKHD1 gene. Symptoms can range from high blood pressure to kidney failure. Treatments aim to control complications through medication and dialysis, with kidney transplantation as an option.
This document discusses anemia management in chronic kidney disease (CKD). It covers the mechanisms of anemia in CKD, including erythropoietin deficiency and iron deficiency. It reviews guidelines for hemoglobin targets and the use of erythropoiesis-stimulating agents (ESAs) to treat anemia. Larger studies on hemoglobin targets in both dialysis and non-dialysis CKD patients, such as the CHOIR and CREATE trials, found higher risks with higher hemoglobin targets and no benefits to quality of life. Iron deficiency is a major cause of ESA treatment failure in CKD patients.
Dokumen tersebut membahas tentang urolithiasis atau batu ginjal dan saluran kemih. Secara ringkas, dokumen menjelaskan definisi, klasifikasi, etiologi, insidensi, faktor risiko, epidemiologi, gejala klinik, komplikasi, dasar diagnosis, pemeriksaan penunjang, dan diagnosis banding dari kondisi tersebut.
The Amazing World Of Fungus And ProtistsTia Hohler
The document provides an overview of protists and fungi, describing their characteristics, types, and roles. It explains that protists are eukaryotic organisms that are not classified as animals, plants or fungi, and describes three main types of protists - animal-like protists (protozoa), plant-like protists (algae), and fungus-like protists. It also discusses the four main types of fungi and their structures and life cycles, as well as commercial and disease-causing fungi.
Urinary calculi are composed of substances normally found in urine that precipitate out of solution to form stones. The most common types of stones found are calcium oxalate, calcium phosphate, uric acid, and cystine. Risk factors for stone formation include dehydration, diet, medical conditions, and anatomical abnormalities. Management involves dietary changes to reduce stone-forming substances in urine, increased fluid intake, and surgical procedures like ESWL or ureteroscopy for stone removal.
Nephrolithiasis, or kidney stones, are common in the United States, affecting around 13% of men and 7% of women. They are formed from substances like calcium, uric acid, cystine, and struvite. Risk factors include gout, UTIs, family history, certain medications, and diet. Symptoms include flank pain, hematuria, and urinary symptoms. Diagnosis involves urinalysis, imaging like ultrasound or CT. Treatment depends on the stone composition but may include increased fluid intake, diet changes, medications, or surgical removal procedures like lithotripsy. Without treatment, stones less than 5mm often pass spontaneously but larger stones usually require removal to prevent reoccurrence or complications
1. Renal stones, also known as kidney stones, form in the urinary tract, including in the kidneys. Common symptoms include intense pain in the flank that may radiate to the groin, as well as hematuria, pyuria, nausea, and vomiting.
2. Diagnosis involves x-rays, ultrasounds, CT scans, and urine tests. Treatment depends on the size and location of the stone and includes analgesics, fluids, dietary changes, extracorporeal shock wave lithotripsy (ESWL), ureteroscopy, and sometimes surgery.
3. Nursing care focuses on pain management, monitoring for complications like infection and obstruction, patient education on prevention of recurrence
Kidney stones develop when minerals clump together and form a solid mass in the urinary tract. Some common causes of kidney stones include dehydration, as drinking less water means urine cannot dilute minerals as effectively. Certain foods high in minerals that form stones, like oxalates, sodium, and animal proteins, can also increase risk, while calcium-rich foods may prevent stones. Some medications, both over-the-counter and prescription, are associated with higher risks of developing kidney stones as a side effect as well.
The document provides information about kidney stones, including their anatomy, causes, types, symptoms, risk factors, complications, prevention, diagnostic procedures, and treatment options. Kidney stones form when there is an excess of stone-forming substances in the urine that causes crystals to form and stick together. Treatment depends on the size and location of the stone, and may involve increased fluid intake, medication to pass stones, procedures to break up stones using sound waves or lasers, or surgery to remove larger stones.
The document discusses renal stones (kidney stones). It defines renal stones as hard mineral deposits that form inside the kidneys. Risk factors include dehydration, family history, obesity, and certain medical conditions. The most common types of stones are calcium and uric acid stones. Symptoms include severe back and abdominal pain, painful urination, and blood in the urine. Diagnosis involves blood and urine tests, along with imaging like ultrasound or CT. Treatment depends on the size and location of the stone but may include increased fluid intake, pain medication, surgery to remove large stones, or lithotripsy to break up stones. Preventing recurrence involves drinking plenty of water and eating a diet low in salt and oxalates
Describe About Kidney stone treatment (1).pdfDevenShahu
Kidney stones are a common and painful condition that affects many individuals worldwide. These small, hard deposits form in the kidneys and can cause a range of symptoms. It's crucial to be aware of the early warning signs of kidney stones so that you can seek medical attention promptly. Dr.Devendu Laxmikant Shah is a well-Known Consultant Urologist and Andrologist in Baner, Pune. In this article, we will explore the signs and symptoms that indicate the presence of kidney stones.
Renal calculus disease, or kidney stone disease, is common in western Maharashtra due to geographic and genetic factors. Recurrence of kidney stones is high due to incomplete stone removal and lack of patient follow up. Complications include urinary tract infections, renal failure, and the need for dialysis. Analyzing stone composition and monitoring urine chemistry can help design diets and medications to prevent recurrence and complications. Doctors must educate patients on recurrence risks and ensure stone analysis to optimize management and prevention of kidney stone disease.
This document provides information about kidney stones (nephrolithiasis). It begins with terminology used to describe stones in different parts of the urinary tract. It then discusses the introduction, definition, etiology, types, pathophysiology, clinical manifestations, diagnostic tests, management, prevention, nursing diagnosis, nursing management, complications, and conclusion of kidney stones. The document aims to educate on kidney stones by defining the condition, describing the causes and types, outlining signs and symptoms, discussing treatment options, prevention methods, and potential complications.
SSurocare as the best choice for kidney stone treatment in Bangalore. Also we provide kidney stone removal at affordable cost Bangalore, Visit for advanced treatment of kidney stone surgery.
Laboratory investigation of kidney disorders,urolithiasis and hypo uricemia ....RituPatil26
The document summarizes laboratory investigations for two kidney disorders:
1) Urolithiasis (kidney stones) - Laboratory tests help diagnose and monitor this condition through urinalysis, imaging scans to detect stones, and blood/urine tests to analyze stone composition. Treatment focuses on diet, hydration and medication.
2) Hypouricemia (low uric acid levels) - This condition is diagnosed through blood and urine testing. Causes include genetics, medications, kidney disease and pregnancy. Symptoms are generally mild but complications can include kidney stones and infections. Treatment addresses underlying causes and may include supplements.
1) Nephrolithiasis, or kidney stones, has an incidence of 1 in 1000 people per year and most commonly affects those aged 20-35, with higher rates in males.
2) Family history is a significant risk factor, with 17.2% of men with a family history developing stones compared to 6.4% without.
3) Recurrence rates of kidney stones are high, reaching 100% over 15-20 years without preventative measures.
Kidney stones are hard mineral deposits that form in the kidneys and can cause painful symptoms when passing through the urinary tract. Symptoms include pain in the back, side, abdomen or groin, as well as nausea, vomiting, blood in the urine, and frequent urination. Kidney stones can be prevented naturally by staying hydrated, eating less animal protein and sodium, and avoiding high-dose vitamin C supplements. Traditional Chinese medicine views kidney stones as caused by damp heat and blockages in the lower body.
Around 12% of the world's population experiences kidney stones. Kidney stones are small, hard deposits of minerals and salts that form on the inner surfaces of the kidneys, bladder, or urinary tract. There are several types of kidney stones that are classified based on their location and mineral composition, with calcium oxalate being the most common. Risk factors for developing kidney stones include a diet high in oxalates or animal proteins, low fluid intake, urinary tract infections, and family history. Symptoms can include pain in the back or abdomen, nausea, blood in the urine, and painful urination. Treatment options depend on the size and location of the stone and may include increased fluid intake, pain medications, lith
Kidney Hospitals in India – Laparoscopic Surgery, Lithotripsy Centre, Dialysi...Dinesh Patel
Devasya Kidney Hospital provides information on kidney disease, protection, and treatment. Chronic kidney disease means the kidneys are less able to filter wastes from the blood and may lead to failure requiring dialysis or transplant. Type 2 diabetes and high blood pressure are the most common causes. The hospital has advanced laparoscopic and lithotripsy centers, a dialysis center, and other facilities for kidney care. It is located in Ahmedabad and was the first in India to use advanced laser technology for prostate procedures.
- Idiopathic calcium oxalate stone-formers are advised to reduce intake of animal protein, oxalate, and sodium while maintaining 800-1200 mg of calcium intake and increasing consumption of citrate and potassium.
- For uric acid stones, the mainstay of therapy is weight loss and urinary alkalinization through a more vegetarian diet, as well as reducing animal protein to decrease purine intake and uric acid excretion.
- Dietary recommendations are based on both stone type and levels of various urinary excretions as measured by 24-hour urine tests.
Kidney stones typically form when minerals in urine crystallize and accumulate in the kidneys or urinary tract. The document discusses kidney stone incidence, types, causes, risk factors, formation process, clinical manifestations, and treatment/prevention options. Treatment depends on stone size and symptoms, and may include increased fluid intake, pain medication, medical therapy to pass stones, surgery to break up or remove large stones, or lifestyle changes to prevent future stone formation.
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This document discusses kidney health and chronic kidney disease. It covers the role of kidneys, causes of kidney stones, signs and symptoms of kidney stones, dietary recommendations for different types of stones, risk factors for chronic kidney disease, goals of renal nutrition therapy, nutritional screening and assessment of dialysis patients, and dietary recommendations for dialysis patients including managing sodium intake. Nutritional counseling is presented as an important part of integrated renal care and management of chronic kidney disease.
Non Surgical or Medical Management of Uretric Stone: A ReviewDrHeena tiwari
This document provides a review of non-surgical medical management options for ureteral stones. It discusses dietary modifications like increasing fluid intake to at least 2 liters per day to help prevent stone recurrence. Medications that increase urinary citrate levels like potassium citrate are also used. Diuretics may help facilitate stone passage by increasing renal fluid output. Herbal formulations are another treatment approach used to prevent stone recurrence. Overall, the review examines the evidence for various lifestyle changes and pharmacological therapies that can help control pain from stones and reduce stone formation without the need for surgery.
Management of kidney stones and JIN product informationA-VPD
Kidney stones can be fatal and may cause blood infection and damage to your kidney. In this presentation we will introduce different kinds of kidney stone management to treat and protect your kidney. Including natural remedy to keep kidney stones from forming and prevent reoccurence.
Also we proudly would like to introduce you made in japan halal certified health supplements for kidney care "JIN".
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1. .
Kidney Stone Causes,
Evaluation and Prevention
Dr. Britton Edgett Tisdale, MD, Urologist
Assistant Professor of Urology
State University of New York at Buffalo
2. Dr. Britton Edgett Tisdale, MD
UBMD Urology
Assistant Professor of Urology, State University of New York at Buffalo
Male Genitourinary Reconstruction, Female Genitourinary Reconstruction,
Urogynecology, Pelvic Prolapse Management Incontinence, Voiding Dysfunction
Neurourology, Laparoscopic and General Urology
Offices:
4233 Maple Road, Amherst, NY, Phone: (716) 725-6277
1020 Youngs Rd, #110, Williamsville, NY Phone:(716) 725-6277
2816 Pleasant Avenue, Hamburg, NY Phone (716) 725-6277
Surgical and Inpatient Services:
Millard Fillmore Suburban Hospital
Buffalo General Hospital
Erie County Medical Center
3. Objectives
1. Why do we make kidney stones
2. Evaluation of those that have recurrent
kidney stones
3. Prevention of kidney stones
Keep in mind, this is the basics only, not a
comprehensive review
4. What are kidney stones made of?
Composition Male Female All
Calcium Oxalates
Calcium Phosphates
Uric Acid & Urates
Struvite
Cystine
Others
73.2
4.7
17.4
1.6
1
2.1
62.9
14.4
10.3
5.0
2.5
4.9
70.1
7.6
15.2
2.8
1.5
4.8
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
5. Why do stones form, in general?
1. Not enough of things that prevent
stones.
2. Too much of things that cause
stones
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
6. Why do stones form in general?
Not enough of things that prevent stones
1.Not enough fluid intake causes low urine volume
Low urine volume is often seen in 24 hour urine
collections in stone formers
Need to drink enough to make 1.5 – 2.0 liters/quarts of
urine per day
Dilutes things in the urine that cause stones.
1.Not enough citrate, magnesium, potassium, etc.
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
7. Why do stones form in general?
Too much of things that cause stones in the urine
Too much acid
Too much calcium
Too much oxalate
Too much sodium
Too much uric acid
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
8. Why do calcium stones form?
Too much calcium in the urine = Hypercalciuria
Idiopathic = we don’t know why
• 50% of calcium stones
Intestinal issue = absorptive hypercalciuria
• High intestinal calcium absorption, more than one cause
Bone issue = resorptive hypercalciuria
• Increased bone resorption putting more calcium in blood
Kidney issue
• Not reabsorbing calcium during urine production
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
9. Why do calcium stones form?
Too much calcium in the urine = Hypercalciuria
1.Parathyroid gland problem = Primary Hyperparathyroidism
5% of calcium stones
Inherited syndrome
1.Too much vitamin D
Taking too much
Producing too much: sarcoidosis
1.Too much calcium intake/absorption (or not enough intake)
2.Too much thyroid hormone
3.Too much sodium intake
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
10. Why do calcium stones form?
Hypocitraturia =Not enough citrate in the urine
1.Normal Excretion is 300 - 900mg/day, (> 1.2
mmol/day)
2.Citrate binds calcium in the urine, preventing stone
formation
3.Lower in High Protein Diets
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
11. Why do oxalate stones form?
Too much oxalate in the urine = hyperoxaluria
1.Too much oxalate intake
2.Not enough calcium intake with meals
3.Too much absorption from intestines
Inflammatory bowel disease
Gastric bypass surgery
1.Not enough pyridoxine (B6) intake
2.Specific genetic mutations affecting oxalate metabolism
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
12. Calcium Oxalate crystals and stone
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
13. Why do uric acid stones form?
Hyperuricosuria = too much uric acid in the urine
1.Low/acid pH in urine decreases solubility
2.Solubility not high in the first place, is ~90mg/L
3.Normal excretion 5-600mg/day = 4-4.5 mmol/day
Intake of certain foods can increase
Some medications can increase
Medical conditions can increase
1.Low urine volume
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
14. Uric Acid crystals can cause Calcium
Oxalate Stones
Small uric acid cystals are a nidus for calcium
oxalate stone formation
Bind Calcium Oxalate
Promote Crystal Growth
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
15. Uric Acid
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
16. Struvite Stones = “Infection Stones”
1. Ammonium magnesium phosphate stones form in
infected urine
2. pH is High [> 7]
3. Bacterial Urease
urea → ammonia → ammonium
1. Proteus, Klebsiella, Pseudomonas, many others
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
18. Other Stones
1. Calcium phosphate
2. Cystine
Genetic “COLA” abnormality
1. Drug Stones
triamterene
Indinavir
Many others
1. Xanthine
Ciprofloxacin
Indinavir
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
19. Renal Tubular Acidosis
1. Distal RTA (Type 1)
Defective Excretion & Retention of
Hydrogen Ions in Urine
Problem with excretion, problem with
trapping
Calcium phosphate stones
Nephrocalcinosis
Non-anion gap metabolic acidosis
Relatively alkaline urine pH
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
20. Evaluation of stone formers
What to Measure
1.24 Hour Urine Collection
2.Blood tests
3.Imaging
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
21. Evaluation of stone formers
24 Hour Urine Collection
Things that cause stones
calcium, phosphate, uric acid, oxalate, sodium
Things that prevent stones
citrate, magnesium, potassiuim
Other things
Volume, creatinine, pH
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
22. Evaluation of stone formers
Blood tests
BMP
Ionizied Calcium & PTH
Vitamin D
TSH
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
23. Evaluation of stone formers
Imaging Studies to evaluate stone size, number, location
Non-contrast CT of the abdomen and pelvis
>/= 95% sensitivity and specificity
Ultrasound + Xray of kidneys + ureters + bladder =
“KUB”
50% sensitive for small stones
Intravenous pyelogram = “IVP” – can be done, but
mostly historical
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
24. Prevention of Calcium Oxalate Stones
1. Dietary and Fluid Intake Modification
2. Medications
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
25. Prevention of Calcium Oxalate Stones
Dietary Modification
Fluid Intake
Animal Protein Intake
Sodium Intake
Calcium Intake
Not what you might think
Oxalate Intake
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
26. Prevention of Calcium Stones
Medications
Hydrochlorthiazide
Reduce calcium in the urine
Phosphates
Bind calcium in the intestines
Potassium Citrate
CaOx, RTA (CaP), Uric acid, Cystine
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
27. Prevention of oxalate stones
1. Calcium taken with meals
binds oxalate in the gut from food
1. Cholestyramine
2. Pyridoxine
3. Magnesium
magnesium oxalate is soluble
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
28. Prevention of Uric Acid Stones
1. Drink more water
2. Restrict dietary purines
3. Medications
Allopurinol
• prevents formation of uric acid
Alkalinize the urine
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
29. Prevention for other types of stones
1. Drink more water
2. Medications
Antibiotics for struvite/“infection” stones
Penicillamine for cystine stones
Other medications
1. Stop medications that may be causing stone
formation.
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
30. Take Home Messages
1. Kidney stones are common (10% lifetime
risk in North America)
2. Kidney stone formation & growth can be
prevented or slowed to reduce the frequency
of need for surgical intervention
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
31. Take Home Messages
Prevention of Kidney Stone Formation &
Growth
Increase urine volume by drinking more water
Avoid excess dietary sodium and animal protein
“Normal” Calcium (1 - 1.5 g/day) intake with
meals (not low or high intake)
Potassium Citrate
CaOx, RTA (CaP), UA, Cystine
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
32. Scenario: Calcium Oxalate Stones
60 year old male
2 episodes of renal colic from ureteral stones
Calcium oxalate stones
Blood tests - normal
Non-contrast CT/CAT scan: no more stones
BEFORE looking at the next slide, what other
test(s) would you order?
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
33. Urine Chemistry from 24 hour urine
collection
1. Volume 1.75 L
2. Calcium 2.9 mmol/day (N 2.5 - 7.5 mmol/d)
3. Oxalate 270 µmol/day (N < 450 µmol/day)
4. Urate 5.5 mmol/day (N < 4.5 mmol/day)
5. Citrate 0.6 mmol/day(N > 1.2 mmol/day)
BEFORE looking at the next slide, what
treatment/prevention measures would you
order?Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/
34. Prevention of Calcium Oxalate Kidney
Stones
1. Drink more fluid = water
2. Avoid excess intake of sodium/salt, oxalate
3. “Normal” animal protein/meat intake
No more than 3 “deck of card” sizes per day
1. “Normal” calcium intake, with meals
2. Take in more citrate (diet or prescription)
3. Medications
Consider hydrochlorothiazide, chlorthalidone
Consider allopurinol (high urine uric acid also can help cause
calcium oxalate stones)
Dr. Britton E. Tisdale, MD, Urologist 716-725-6277 ubmdurology.com/contact/