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==Overview==
Nephrolithiasis  is a common condition encountered in emergency rooms and also as an outpatient in the primary care setting. Its incidence and prevalence is increasing both in women and men, with women slightly incraing recently due to [[obesity]] and lifestyle changes. Nephrolithiasis may be classified into 4 subtypes/groups: calcium stones, [[struvite]] stones[[Uric acid nephrolithiasis|, uric acid stones]] and [[cystine]] stones. The common causes of nephrolithiasis include [[hypercalcemia]], [[hyperparathyroidism]], [[hypercalciuria]], infection with urea splitting microorganisms like [[Proteus]] and [[Pseudomonas]], [[gout]], [[dehydration]], [[inflammatory bowel disease]]. Less common causes of nephrolithiasis include drugs such as [[loop diuretics]][[Acetazolamide|, Acetazolamide]], [[ciprofloxacin]], [[indinavir]], [[guaifenesin]] [[triamterene]] and [[magnesium trisilicate]]. It is understood that nephrolithiasis is the result of combination of different mechanism responsible for different types of stones. Calcium stones are the most common type of kidney stones. Approximately 80% of all calcium stones are [[calcium oxalate]] stones. The pathophysiology of calcium stones is complex and involves dietary concerns, [[hypercalciuria]], [[hypocitaturia]], [[hyperoxaluria]][[Hyperuricosuria|, hyperuricosuria]] and biomineralization. The underlying pathophysiological mechanisms responsible for uric acid stones are low urine volume[[Hyperuricosuria|, hyperuricosuria]] and high acidic urine. [[Cystinuria]] is a rare hereditary gene disorder which causes impaired renal reabsorption of cationic amino acids and cystine. It is caused by mutations in either of the two subunits (rBAT(SLC3A2) and b0,+AT(SLC7A9)) forming cystine stones. Struvite stones are usually seen in patients which have infection with [[urease]] +ve organisms. Urine pH is usually alkaline (>7.2). Nephrolithiasis can be passed on to following generations due to rare causes of hypercalciuria such as hereditary [[distal renal tubular acidosis]], [[dent disease]], [[Bartter syndrome]] types III and IV, autosomal dominant hypocalcemic hypercalciuria and familial [[hypomagnesemia]]. Nephrolithiasis associated with [[Hyperparathyroidism]], [[Gout]], [[Hypocitaturia]], [[Sarcoidosis]], chronic [[urinary tract infections]] and [[Obesity]].On gross pathology, the characteristic findings of nephrolithiasis include location = 80% unilateral, usually in calyces, pelvis or bladder. The size=variable, 2-3 mm usually. All stones contain an organic matrix of mucoprotein. The shape of struvite stone is staghorn shaped. On microscopic histopathological analysis, the characteristic findings of nephrolithiasis include different shapes of stones/crystals are such as cystine= hexagonal, struvite= coffin lid shape, calcium oxalate= pyramid shape to dumbbell shape and [[uric acid]]= rectangular/rhomboidal. Oxalate crystals are highlighted by polarized light. Also, foreign body giant cells and macrophages are seen with the stones.It has increased from every 1 in 20 to 1 in 11 person in United States has kidney stones. If left untreated, <30% of patients with nephrolithiasis may progress to develop renal colicky pain due to increase in rate of growth.Most of the stones pass spontaneously. about 10-20% of symptom-causing stones fail to pass. Lower poles stones were significantly less likely to cause symptoms or pass spontaneously. They can progress to hydronephrosis especially when combined or superimposed by u[[Urinary tract infection|rinary tract infection]]. Common complications of nephrolithiasis include [[hydronephrosis]], [[chronic renal failure]], [[hypertension]], [[cardiovascular disease]], and increased risk of fracture. Prognosis is generally excellent. Approximately 80-85% resolve spontaneously. Recurrence rates for calcium stones after the initial event is 40–50% at the end of 5 years and 50–60% at the end of 10 years.The patients with nephrolithiasis may have a positive history of [[flank pain]]. Common symptoms of nephrolithiasis include [[flank pain]] progressing downward and anteriorly into the groin as the stone moves, [[hematuria]], [[nausea and vomiting]] urinary frequency and urgency. Less common symptoms include burning [[micturition]]. Patients with nephrolithiasis usually appear in pain and trying to achieve a comfortable position. Common physical examination findings of nephrolithiasis include [[costovertebral angle]] tenderness, may accompany fever with increased heart rate and respiratory rate. They can have hypoactive bowel sounds due to ileus caused by severe pain. They can have hematuria in microscopic exmaination. Laboratory findings consistent with the diagnosis of nephrolithiasis include [[hypercalcemia]], [[hypercalciuria]], [[hyperoxaluria]], [[hypocitraturia]], [[hyperuricemia]] and [[hyperuricosuria]]. Abdominal ultrasound may be helpful in the diagnosis of nephrolithiasis Findings on an ultrasound suggestive of/diagnostic of nephrolithiasis include: echogenic or hyperechogenic foci, acoustic shadowing, twinkle artefact on colour Doppler, colour comet-tail artefact , and increased resistive index which signifies acute obstruction. CT scan is the gold standard test for the diagnosis of nephrolithiasis. Abdominal and pelvic CT scan is helpful in the diagnosis of nephrolithiasis. Findings on CT scan diagnostic of nephrolithiasis include radiopacity showing the location, density and composition of stones [[calcium oxalate]] +/- [[calcium phosphate]]: 400-600 HU, [[struvite]] (triple phosphate): usually opaque but variable, pure [[calcium phosphate]] 400-600 HU, [[uric acid]]: 100-200 HU and [[cystine]]: opaque. The treatment of nephrolithiasis involves different measures e.g non pharmacological measures consisting of increased fluid intake, straining an dietary restrictions. Pharmacological measures include pain relief using NSAIDs and opioids., helping passage of stone spontaneously with drugs like [[tamsulosin]] and [[nifedipine]]. The treatment of underlying cause and being specific to type of stones is very important.It involves treating [[Hyperparathyroidism medical therapy|primary hyperparathyroidism]] and [[Renal tubular acidosis]]. For those having high urinary calcium, [[Hydrochlorothiazide]] or [[Chlorthalidone]] are used. For recurrent stones and high urine [[uric acid]], [[Allopurinol]] is used. For recurrent stones and [[hypocitraturia]], [[Potassium citrate]] is sued to alkalinize the urine. For uric acid stones, alkalinizing urine with [[potassium citrate]]/[[potassium bicarbonate]] is done and if needed [[Allopurinol]] is also used. For struvite stones, medical therapy is not of much help, although urease inhibitors such as [[Acetohydroxamic Acid|acetohydroxamic acid]] can be given in urease +ve etiology. For cysteine stones, again alkalinizing urine helps along with [[Tiopronin]]. The Urological consult is needed when stone >10 mm in diameter, uncontrolled pain, [[Anuria]], or there is [[Acute kidney injury]]. The mainstay of treatment for nephrolithiasis is medical therapy. Surgery is usually reserved for patients with either persistent and severe pain, [[renal failure]], kidney infection and when stone fails to pass or move after 30 days. The surgeries which are being used currently include [[extracorporeal shockwave lithotripsy]], [[ureteroscopy]] and percutaneous nephrolithotomy. Effective measures for the primary prevention of nephrolithiais include diet control and high fluid intake. Effective measures for the secondary prevention of nephrolithiasis include measures to prevent recurrence of the stones and prevent complications. It includes measures like correcting hydration and dietary habits. Drugs like [[allopurinol]] to prevent [[hyperuricemia]], [[potassium citrate]] to alkalinize the urine and avoidance or judicious use of diuretics.
 
==Historical Perspective==
Urinary stones was first discovered by  E. Smith, an English archaeologist, in 1901 when he found bladder stone in Egyptian mummy aged 4500-7000 year. In the 4th century B.C., when [[Hippocrates|Hipprocratic]] Oath was made,the line that refers to stones was mentioned: '' “I will not use the knife, not even on sufferers from stone, but will withdraw in favor of such men as are engaged in this work....I will not cut for the stone, but will leave this to be done by practitioners of this work.”''In the 8th century B.C, treatment strategy for stone removal was developed by an Indian surgeon, [[Sushruta]] as written in [[Sushruta Samhita]]. In 1976, the first percutaneous stone surgery was performed by Fernstrom and Johansson. The famous cases of nephrolithiasis includes: in 1549, Michelangelo was diagnosed and treated for uric acid stones;in 1724, Sir [[Isaac Newton]] noted that he passed two small pea-sized stones and in 1961, Roger Moore, aka James Bond, experienced three kidney stone episodes and treated with surgery.


==Overview==
==Classification==
'''Kidney stones''', also called '''renal [[Calculus (medicine)|calculi]]''', are solid concretions (crystal aggregations) of dissolved [[dietary mineral|minerals]] in [[urine]]; calculi typically form inside the [[kidney]]s or [[bladder]]. The terms ''nephrolithiasis'' and ''urolithiasis'' refer to the presence of calculi in the kidneys and urinary tract, respectively.   
Nephrolithiasis may be classified into 4 subtypes/groups: calcium stones, [[struvite]] stones[[Uric acid nephrolithiasis|, uric acid stones]] and [[cystine]] stones
 
==Pathophysiology==
It is understood that nephrolithiasis is the result of combination of different mechanism responsible for different types of stones. Calcium stones are the most common type of kidney stones. Approximately 80% of all calcium stones are [[calcium oxalate]] stones. The pathophysiology of calcium stones is complex and involves dietary concerns, [[hypercalciuria]], [[hypocitaturia]], [[hyperoxaluria]][[Hyperuricosuria|, hyperuricosuria]] and biomineralization. The underlying pathophysiological mechanisms responsible for uric acid stones are low urine volume[[Hyperuricosuria|, hyperuricosuria]] and high acidic urine. [[Cystinuria]] is a rare hereditary gene disorder which causes impaired renal reabsorption of cationic amino acids and cystine. It is caused by mutations in either of the two subunits (rBAT(SLC3A2) and b0,+AT(SLC7A9)) forming cystine stones. Struvite stones are usually seen in patients which have infection with [[urease]] +ve organisms. Urine pH is usually alkaline (>7.2). Nephrolithiasis can be passed on to following generations due to rare causes of hypercalciuria such as hereditary [[distal renal tubular acidosis]], [[dent disease]], [[Bartter syndrome]] types III and IV, autosomal dominant hypocalcemic hypercalciuria and familial [[hypomagnesemia]]. Nephrolithiasis associated with [[Hyperparathyroidism]], [[Gout]], [[Hypocitaturia]], [[Sarcoidosis]], chronic [[urinary tract infections]] and [[Obesity]].On gross pathology, the characteristic findings of nephrolithiasis include location = 80% unilateral, usually in calyces, pelvis or bladder. The size=variable, 2-3 mm usually. All stones contain an organic matrix of mucoprotein. The shape of struvite stone is staghorn shaped. On microscopic histopathological analysis, the characteristic findings of nephrolithiasis include different shapes of stones/crystals are such as cystine= hexagonal, struvite= coffin lid shape, calcium oxalate= pyramid shape to dumbbell shape and [[uric acid]]= rectangular/rhomboidal. Oxalate crystals are highlighted by polarized light. Also, foreign body giant cells and macrophages are seen with the stones.
 
==Causes==
The common causes of nephrolithiasis include [[hypercalcemia]], [[hyperparathyroidism]], [[hypercalciuria]], infection with urea splitting microorganisms like [[Proteus]] and [[Pseudomonas]], [[gout]], [[dehydration]], [[inflammatory bowel disease]]. Less common causes of nephrolithiasis include drugs such as [[loop diuretics]][[Acetazolamide|, Acetazolamide]], [[ciprofloxacin]], [[indinavir]], [[guaifenesin]] [[triamterene]] and [[magnesium trisilicate]].
 
==Differentiating Nephrolithiasis from Other Diseases==
Nephrolithiasis should be differentiated from other conditions presenting with [[Flank Pain|acute flank]] or [[upper abdominal pain]], [[hematuria]], [[nausea and vomiting]].
 
==Epidemiology and Demographics==
In 2000, the incidence/prevalence of nephrolithiasis was estimated to be 116 cases per 100,000 individuals in the United States.The prevalence of nephrolithiasis is approximately 1116 per 100,000 individuals worldwide. It has increased from every 1 in 20 to 1 in 11 person in United States has kidney stones. According to American Journal of Kidney disease, 2016, 8% of women and 16% of men are developing nephrolithiasis by the age of 70 years. According to 2000 National Hospital Ambulatory Medical Care Survey of the United State,s there is an annual burden of more than 1,100,000 emergency department visits with a primary diagnosis of renal calculus or colic. Patients of all age groups may develop nephrolithiasis. The incidence of nephrolithiasis increases with age.  At initial diagnosis, the mean age was 44.8 years in men and 40.9 years in women. Nephrolithiasis usually affects individuals of the white/Caucasian ethnicity. Males are more commonly affected by nephrolithiaisis than females. The male to female ratio is approximately 2 to 1. The trend keeps on changing , a study in 2010 claims the incidence rate ratio of men to women with urinary tract stones has narrowed from 3.4 to 1.3. Females are having increasing incidence rates owing to increase lifestyle disease like [[obesity]]. The majority of nephrolithiasis cases are reported in southeast belt of the United States. The number of cases increase from north to south and from west to east. The states of North Carolina, South Carolina, Georgia, Alabama, Mississippi, and Tennessee are considered in the “stone belt.” The ambient temperature and sunlight levels as risk factors for stones and differences in exposure to temperature and sunlight and beverages are also responsible for geographic variability.
 
==Risk Factors==
Common risk factors in the development of nephrolithiasis include dietary habits, low urinary pH, [[hypercalcemia]], [[hypercalciuria]], [[hyperoxaluria]], [[hyperuricemia]], [[hyperuricosuria]], [[obesity]], [[diabetes mellitus]], environmental factors such as hot climate, drugs such as [[thiazide]], [[furosemide]], [[sulfadiazine]], [[indinavir]]. Less common risk factors in the development of nephrolithiasis include [[hypocitraturia]], beverage use, drugs like [[ciprofloxacin]] and [[triamterene]].
 
==Screening==
There is insufficient evidence to recommend routine screening for nephrolithiaisis.
 
==Natural History, Complications, and Prognosis==
 
If left untreated, <30% of patients with nephrolithiasis may progress to develop renal colicky pain due to increase in rate of growth.Most of the stones pass spontaneously. about 10-20% of symptom-causing stones fail to pass. Lower poles stones were significantly less likely to cause symptoms or pass spontaneously. They can progress to hydronephrosis especially when combined or superimposed by u[[Urinary tract infection|rinary tract infection]]. Common complications of nephrolithiasis include [[hydronephrosis]], [[chronic renal failure]], [[hypertension]], [[cardiovascular disease]], and increased risk of fracture. Prognosis is generally excellent. Approximately 80-85% resolve spontaneously. Recurrence rates for calcium stones after the initial event is 40–50% at the end of 5 years and 50–60% at the end of 10 years.
==Diagnosis==
===Diagnostic Study of choice===
CT scan is the gold standard test for the diagnosis of nephrolithiasis.
 
===History and Symptoms===
The patients with nephrolithiasis may have a positive history of [[flank pain]]. Common symptoms of nephrolithiasis include [[flank pain]] progressing downward and anteriorly into the groin as the stone moves, [[hematuria]], [[nausea and vomiting]] urinary frequency and urgency. Less common symptoms include burning [[micturition]].
 
===Physical Examination===
Patients with nephrolithiasis usually appear in pain and trying to achieve a comfortable position. Common physical examination findings of nephrolithiasis include [[costovertebral angle]] tenderness, may accompany fever with increased heart rate and respiratory rate. They can have hypoactive bowel sounds due to ileus caused by severe pain. They can have hematuria in microscopic exmaination.
 
===Laboratory Findings===
Laboratory findings consistent with the diagnosis of nephrolithiasis include [[hypercalcemia]], [[hypercalciuria]], [[hyperoxaluria]], [[hypocitraturia]], [[hyperuricemia]] and [[hyperuricosuria]].
 
===Electrocardiogram===
There are no ECG findings associated with nephrolithiasis.
 
===X-ray===
An x-ray may be helpfulin the diagnosis of nephrolithiasis. Findings on an x-ray suggestive of nephrolithiasis include radiopaque stones such as [[Calcium oxalate]], [[calcium phosphate]], [[struvite]] and radiolucent stones which includes [[uric acid]] stones and [[cystine]] stones.
 
===Ultrasound===
Abdominal ultrasound may be helpful in the diagnosis of nephrolithiasis Findings on an ultrasound suggestive of/diagnostic of nephrolithiasis include: echogenic or hyperechogenic foci, acoustic shadowing, twinkle artefact on colour Doppler, colour comet-tail artefact , and increased resistive index which signifies acute obstruction.
 
===CT scan===
Abdominal and pelvic CT scan is helpful in the diagnosis of nephrolithiasis. Findings on CT scan diagnostic of nephrolithiasis include radiopacity showing the location, density and composition of stones [[calcium oxalate]] +/- [[calcium phosphate]]: 400-600 HU, [[struvite]] (triple phosphate): usually opaque but variable, pure [[calcium phosphate]] 400-600 HU, [[uric acid]]: 100-200 HU and [[cystine]]: opaque.
 
===MRI===
There are no MRI findings associated with nephrolithiasis. However, a MRI may be helpful in the diagnosis of complications of nephrolithiasis, which include [[hydronephrosis]].
 
===Other Imaging Findings===
There are no other imaging findings associated with nephrolithiasis.
 
===Other Diagnostic Studies===
There are no other diagnostic studies associated with nephrolithiasis.
 
==Treatment==
===Medical Therapy===
The treatment of nephrolithiasis involves different measures e.g non pharmacological measures consisting of increased fluid intake, straining an dietary restrictions. Pharmacological measures include pain relief using NSAIDs and opioids., helping passage of stone spontaneously with drugs like [[tamsulosin]] and [[nifedipine]]. The treatment of underlying cause and being specific to type of stones is very important.It involves treating [[Hyperparathyroidism medical therapy|primary hyperparathyroidism]] and [[Renal tubular acidosis]]. For those having high urinary calcium, [[Hydrochlorothiazide]] or [[Chlorthalidone]] are used. For recurrent stones and high urine [[uric acid]], [[Allopurinol]] is used. For recurrent stones and [[hypocitraturia]], [[Potassium citrate]] is sued to alkalinize the urine. For uric acid stones, alkalinizing urine with [[potassium citrate]]/[[potassium bicarbonate]] is done and if needed [[Allopurinol]] is also used. For struvite stones, medical therapy is not of much help, although urease inhibitors such as [[Acetohydroxamic Acid|acetohydroxamic acid]] can be given in urease +ve etiology. For cysteine stones, again alkalinizing urine helps along with [[Tiopronin]]. The Urological consult is needed when stone >10 mm in diameter, uncontrolled pain, [[Anuria]], or there is [[Acute kidney injury]].
 
===Surgery===
The mainstay of treatment for nephrolithiasis is medical therapy. Surgery is usually reserved for patients with either persistent and severe pain, [[renal failure]], kidney infection and when stone fails to pass or move after 30 days. The surgeries which are being used currently include [[extracorporeal shockwave lithotripsy]], [[ureteroscopy]] and percutaneous nephrolithotomy.
 
===Primary Prevention===
Effective measures for the primary prevention of nephrolithiais include diet control and high fluid intake.


Renal calculi can vary in size from as small as grains of sand to as large as grapefruit. 
===Secondary Prevention===
Kidney stones typically leave the body by passage in the urine stream, and many stones are formed and passed without causing symptoms. If stones grow to sufficient size before passage &mdash; on the order of at least 2-3 millimeters &mdash; they can cause obstruction of the ureter. The resulting obstruction with dilation or stretching of the upper ureter and renal pelvis as well as spasm of muscle, trying to move the stone, can cause severe episodic [[Pain and nociception|pain]], most commonly felt in the [[flank]], lower abdomen and groin (a condition called [[renal colic]]).  Renal colic can be associated with nausea and vomiting due to the [[embryology|embyrological]] association of the kidneys with the intestinal tract. [[Hematuria]] (bloody urine) is commonly present due to damage to the lining of the urinary tract. Recurrence rates are estimated at about 10% per year.  Men are affected approximately 4 times more often than women.
Effective measures for the secondary prevention of nephrolithiasis include measures to prevent recurrence of the stones and prevent complications. It includes measures like correcting hydration and dietary habits. Drugs like [[allopurinol]] to prevent [[hyperuricemia]], [[potassium citrate]] to alkalinize the urine and avoidance or judicious use of diuretics.


==References==
==References==
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Amandeep Singh M.D.[2]

Overview

Nephrolithiasis is a common condition encountered in emergency rooms and also as an outpatient in the primary care setting. Its incidence and prevalence is increasing both in women and men, with women slightly incraing recently due to obesity and lifestyle changes. Nephrolithiasis may be classified into 4 subtypes/groups: calcium stones, struvite stones, uric acid stones and cystine stones. The common causes of nephrolithiasis include hypercalcemiahyperparathyroidismhypercalciuria, infection with urea splitting microorganisms like Proteus and Pseudomonasgoutdehydrationinflammatory bowel disease. Less common causes of nephrolithiasis include drugs such as loop diuretics, Acetazolamideciprofloxacinindinavirguaifenesin triamterene and magnesium trisilicate. It is understood that nephrolithiasis is the result of combination of different mechanism responsible for different types of stones. Calcium stones are the most common type of kidney stones. Approximately 80% of all calcium stones are calcium oxalate stones. The pathophysiology of calcium stones is complex and involves dietary concerns, hypercalciuriahypocitaturiahyperoxaluria, hyperuricosuria and biomineralization. The underlying pathophysiological mechanisms responsible for uric acid stones are low urine volume, hyperuricosuria and high acidic urine. Cystinuria is a rare hereditary gene disorder which causes impaired renal reabsorption of cationic amino acids and cystine. It is caused by mutations in either of the two subunits (rBAT(SLC3A2) and b0,+AT(SLC7A9)) forming cystine stones. Struvite stones are usually seen in patients which have infection with urease +ve organisms. Urine pH is usually alkaline (>7.2). Nephrolithiasis can be passed on to following generations due to rare causes of hypercalciuria such as hereditary distal renal tubular acidosisdent diseaseBartter syndrome types III and IV, autosomal dominant hypocalcemic hypercalciuria and familial hypomagnesemia. Nephrolithiasis associated with HyperparathyroidismGoutHypocitaturiaSarcoidosis, chronic urinary tract infections and Obesity.On gross pathology, the characteristic findings of nephrolithiasis include location = 80% unilateral, usually in calyces, pelvis or bladder. The size=variable, 2-3 mm usually. All stones contain an organic matrix of mucoprotein. The shape of struvite stone is staghorn shaped. On microscopic histopathological analysis, the characteristic findings of nephrolithiasis include different shapes of stones/crystals are such as cystine= hexagonal, struvite= coffin lid shape, calcium oxalate= pyramid shape to dumbbell shape and uric acid= rectangular/rhomboidal. Oxalate crystals are highlighted by polarized light. Also, foreign body giant cells and macrophages are seen with the stones.It has increased from every 1 in 20 to 1 in 11 person in United States has kidney stones. If left untreated, <30% of patients with nephrolithiasis may progress to develop renal colicky pain due to increase in rate of growth.Most of the stones pass spontaneously. about 10-20% of symptom-causing stones fail to pass. Lower poles stones were significantly less likely to cause symptoms or pass spontaneously. They can progress to hydronephrosis especially when combined or superimposed by urinary tract infection. Common complications of nephrolithiasis include hydronephrosischronic renal failurehypertensioncardiovascular disease, and increased risk of fracture. Prognosis is generally excellent. Approximately 80-85% resolve spontaneously. Recurrence rates for calcium stones after the initial event is 40–50% at the end of 5 years and 50–60% at the end of 10 years.The patients with nephrolithiasis may have a positive history of flank pain. Common symptoms of nephrolithiasis include flank pain progressing downward and anteriorly into the groin as the stone moves, hematurianausea and vomiting urinary frequency and urgency. Less common symptoms include burning micturition. Patients with nephrolithiasis usually appear in pain and trying to achieve a comfortable position. Common physical examination findings of nephrolithiasis include costovertebral angle tenderness, may accompany fever with increased heart rate and respiratory rate. They can have hypoactive bowel sounds due to ileus caused by severe pain. They can have hematuria in microscopic exmaination. Laboratory findings consistent with the diagnosis of nephrolithiasis include hypercalcemiahypercalciuriahyperoxaluriahypocitraturiahyperuricemia and hyperuricosuria. Abdominal ultrasound may be helpful in the diagnosis of nephrolithiasis Findings on an ultrasound suggestive of/diagnostic of nephrolithiasis include: echogenic or hyperechogenic foci, acoustic shadowing, twinkle artefact on colour Doppler, colour comet-tail artefact , and increased resistive index which signifies acute obstruction. CT scan is the gold standard test for the diagnosis of nephrolithiasis. Abdominal and pelvic CT scan is helpful in the diagnosis of nephrolithiasis. Findings on CT scan diagnostic of nephrolithiasis include radiopacity showing the location, density and composition of stones calcium oxalate +/- calcium phosphate: 400-600 HU, struvite (triple phosphate): usually opaque but variable, pure calcium phosphate 400-600 HU, uric acid: 100-200 HU and cystine: opaque. The treatment of nephrolithiasis involves different measures e.g non pharmacological measures consisting of increased fluid intake, straining an dietary restrictions. Pharmacological measures include pain relief using NSAIDs and opioids., helping passage of stone spontaneously with drugs like tamsulosin and nifedipine. The treatment of underlying cause and being specific to type of stones is very important.It involves treating primary hyperparathyroidism and Renal tubular acidosis. For those having high urinary calcium, Hydrochlorothiazide or Chlorthalidone are used. For recurrent stones and high urine uric acidAllopurinol is used. For recurrent stones and hypocitraturiaPotassium citrate is sued to alkalinize the urine. For uric acid stones, alkalinizing urine with potassium citrate/potassium bicarbonate is done and if needed Allopurinol is also used. For struvite stones, medical therapy is not of much help, although urease inhibitors such as acetohydroxamic acid can be given in urease +ve etiology. For cysteine stones, again alkalinizing urine helps along with Tiopronin. The Urological consult is needed when stone >10 mm in diameter, uncontrolled pain, Anuria, or there is Acute kidney injury. The mainstay of treatment for nephrolithiasis is medical therapy. Surgery is usually reserved for patients with either persistent and severe pain, renal failure, kidney infection and when stone fails to pass or move after 30 days. The surgeries which are being used currently include extracorporeal shockwave lithotripsyureteroscopy and percutaneous nephrolithotomy. Effective measures for the primary prevention of nephrolithiais include diet control and high fluid intake. Effective measures for the secondary prevention of nephrolithiasis include measures to prevent recurrence of the stones and prevent complications. It includes measures like correcting hydration and dietary habits. Drugs like allopurinol to prevent hyperuricemiapotassium citrate to alkalinize the urine and avoidance or judicious use of diuretics.

Historical Perspective

Urinary stones was first discovered by  E. Smith, an English archaeologist, in 1901 when he found bladder stone in Egyptian mummy aged 4500-7000 year. In the 4th century B.C., when Hipprocratic Oath was made,the line that refers to stones was mentioned:  “I will not use the knife, not even on sufferers from stone, but will withdraw in favor of such men as are engaged in this work....I will not cut for the stone, but will leave this to be done by practitioners of this work.”In the 8th century B.C, treatment strategy for stone removal was developed by an Indian surgeon, Sushruta as written in Sushruta Samhita. In 1976, the first percutaneous stone surgery was performed by Fernstrom and Johansson. The famous cases of nephrolithiasis includes: in 1549, Michelangelo was diagnosed and treated for uric acid stones;in 1724, Sir Isaac Newton noted that he passed two small pea-sized stones and in 1961, Roger Moore, aka James Bond, experienced three kidney stone episodes and treated with surgery.

Classification

Nephrolithiasis may be classified into 4 subtypes/groups: calcium stones, struvite stones, uric acid stones and cystine stones

Pathophysiology

It is understood that nephrolithiasis is the result of combination of different mechanism responsible for different types of stones. Calcium stones are the most common type of kidney stones. Approximately 80% of all calcium stones are calcium oxalate stones. The pathophysiology of calcium stones is complex and involves dietary concerns, hypercalciuriahypocitaturiahyperoxaluria, hyperuricosuria and biomineralization. The underlying pathophysiological mechanisms responsible for uric acid stones are low urine volume, hyperuricosuria and high acidic urine. Cystinuria is a rare hereditary gene disorder which causes impaired renal reabsorption of cationic amino acids and cystine. It is caused by mutations in either of the two subunits (rBAT(SLC3A2) and b0,+AT(SLC7A9)) forming cystine stones. Struvite stones are usually seen in patients which have infection with urease +ve organisms. Urine pH is usually alkaline (>7.2). Nephrolithiasis can be passed on to following generations due to rare causes of hypercalciuria such as hereditary distal renal tubular acidosisdent diseaseBartter syndrome types III and IV, autosomal dominant hypocalcemic hypercalciuria and familial hypomagnesemia. Nephrolithiasis associated with HyperparathyroidismGoutHypocitaturiaSarcoidosis, chronic urinary tract infections and Obesity.On gross pathology, the characteristic findings of nephrolithiasis include location = 80% unilateral, usually in calyces, pelvis or bladder. The size=variable, 2-3 mm usually. All stones contain an organic matrix of mucoprotein. The shape of struvite stone is staghorn shaped. On microscopic histopathological analysis, the characteristic findings of nephrolithiasis include different shapes of stones/crystals are such as cystine= hexagonal, struvite= coffin lid shape, calcium oxalate= pyramid shape to dumbbell shape and uric acid= rectangular/rhomboidal. Oxalate crystals are highlighted by polarized light. Also, foreign body giant cells and macrophages are seen with the stones.

Causes

The common causes of nephrolithiasis include hypercalcemiahyperparathyroidismhypercalciuria, infection with urea splitting microorganisms like Proteus and Pseudomonasgoutdehydrationinflammatory bowel disease. Less common causes of nephrolithiasis include drugs such as loop diuretics, Acetazolamideciprofloxacinindinavirguaifenesin triamterene and magnesium trisilicate.

Differentiating Nephrolithiasis from Other Diseases

Nephrolithiasis should be differentiated from other conditions presenting with acute flank or upper abdominal painhematurianausea and vomiting.

Epidemiology and Demographics

In 2000, the incidence/prevalence of nephrolithiasis was estimated to be 116 cases per 100,000 individuals in the United States.The prevalence of nephrolithiasis is approximately 1116 per 100,000 individuals worldwide. It has increased from every 1 in 20 to 1 in 11 person in United States has kidney stones. According to American Journal of Kidney disease, 2016, 8% of women and 16% of men are developing nephrolithiasis by the age of 70 years. According to 2000 National Hospital Ambulatory Medical Care Survey of the United State,s there is an annual burden of more than 1,100,000 emergency department visits with a primary diagnosis of renal calculus or colic. Patients of all age groups may develop nephrolithiasis. The incidence of nephrolithiasis increases with age.  At initial diagnosis, the mean age was 44.8 years in men and 40.9 years in women. Nephrolithiasis usually affects individuals of the white/Caucasian ethnicity. Males are more commonly affected by nephrolithiaisis than females. The male to female ratio is approximately 2 to 1. The trend keeps on changing , a study in 2010 claims the incidence rate ratio of men to women with urinary tract stones has narrowed from 3.4 to 1.3. Females are having increasing incidence rates owing to increase lifestyle disease like obesity. The majority of nephrolithiasis cases are reported in southeast belt of the United States. The number of cases increase from north to south and from west to east. The states of North Carolina, South Carolina, Georgia, Alabama, Mississippi, and Tennessee are considered in the “stone belt.” The ambient temperature and sunlight levels as risk factors for stones and differences in exposure to temperature and sunlight and beverages are also responsible for geographic variability.

Risk Factors

Common risk factors in the development of nephrolithiasis include dietary habits, low urinary pH, hypercalcemiahypercalciuriahyperoxaluriahyperuricemiahyperuricosuriaobesitydiabetes mellitus, environmental factors such as hot climate, drugs such as thiazidefurosemidesulfadiazineindinavir. Less common risk factors in the development of nephrolithiasis include hypocitraturia, beverage use, drugs like ciprofloxacin and triamterene.

Screening

There is insufficient evidence to recommend routine screening for nephrolithiaisis.

Natural History, Complications, and Prognosis

If left untreated, <30% of patients with nephrolithiasis may progress to develop renal colicky pain due to increase in rate of growth.Most of the stones pass spontaneously. about 10-20% of symptom-causing stones fail to pass. Lower poles stones were significantly less likely to cause symptoms or pass spontaneously. They can progress to hydronephrosis especially when combined or superimposed by urinary tract infection. Common complications of nephrolithiasis include hydronephrosischronic renal failurehypertensioncardiovascular disease, and increased risk of fracture. Prognosis is generally excellent. Approximately 80-85% resolve spontaneously. Recurrence rates for calcium stones after the initial event is 40–50% at the end of 5 years and 50–60% at the end of 10 years.

Diagnosis

Diagnostic Study of choice

CT scan is the gold standard test for the diagnosis of nephrolithiasis.

History and Symptoms

The patients with nephrolithiasis may have a positive history of flank pain. Common symptoms of nephrolithiasis include flank pain progressing downward and anteriorly into the groin as the stone moves, hematurianausea and vomiting urinary frequency and urgency. Less common symptoms include burning micturition.

Physical Examination

Patients with nephrolithiasis usually appear in pain and trying to achieve a comfortable position. Common physical examination findings of nephrolithiasis include costovertebral angle tenderness, may accompany fever with increased heart rate and respiratory rate. They can have hypoactive bowel sounds due to ileus caused by severe pain. They can have hematuria in microscopic exmaination.

Laboratory Findings

Laboratory findings consistent with the diagnosis of nephrolithiasis include hypercalcemiahypercalciuriahyperoxaluriahypocitraturiahyperuricemia and hyperuricosuria.

Electrocardiogram

There are no ECG findings associated with nephrolithiasis.

X-ray

An x-ray may be helpfulin the diagnosis of nephrolithiasis. Findings on an x-ray suggestive of nephrolithiasis include radiopaque stones such as Calcium oxalate, calcium phosphatestruvite and radiolucent stones which includes uric acid stones and cystine stones.

Ultrasound

Abdominal ultrasound may be helpful in the diagnosis of nephrolithiasis Findings on an ultrasound suggestive of/diagnostic of nephrolithiasis include: echogenic or hyperechogenic foci, acoustic shadowing, twinkle artefact on colour Doppler, colour comet-tail artefact , and increased resistive index which signifies acute obstruction.

CT scan

Abdominal and pelvic CT scan is helpful in the diagnosis of nephrolithiasis. Findings on CT scan diagnostic of nephrolithiasis include radiopacity showing the location, density and composition of stones calcium oxalate +/- calcium phosphate: 400-600 HU, struvite (triple phosphate): usually opaque but variable, pure calcium phosphate 400-600 HU, uric acid: 100-200 HU and cystine: opaque.

MRI

There are no MRI findings associated with nephrolithiasis. However, a MRI may be helpful in the diagnosis of complications of nephrolithiasis, which include hydronephrosis.

Other Imaging Findings

There are no other imaging findings associated with nephrolithiasis.

Other Diagnostic Studies

There are no other diagnostic studies associated with nephrolithiasis.

Treatment

Medical Therapy

The treatment of nephrolithiasis involves different measures e.g non pharmacological measures consisting of increased fluid intake, straining an dietary restrictions. Pharmacological measures include pain relief using NSAIDs and opioids., helping passage of stone spontaneously with drugs like tamsulosin and nifedipine. The treatment of underlying cause and being specific to type of stones is very important.It involves treating primary hyperparathyroidism and Renal tubular acidosis. For those having high urinary calcium, Hydrochlorothiazide or Chlorthalidone are used. For recurrent stones and high urine uric acidAllopurinol is used. For recurrent stones and hypocitraturiaPotassium citrate is sued to alkalinize the urine. For uric acid stones, alkalinizing urine with potassium citrate/potassium bicarbonate is done and if needed Allopurinol is also used. For struvite stones, medical therapy is not of much help, although urease inhibitors such as acetohydroxamic acid can be given in urease +ve etiology. For cysteine stones, again alkalinizing urine helps along with Tiopronin. The Urological consult is needed when stone >10 mm in diameter, uncontrolled pain, Anuria, or there is Acute kidney injury.

Surgery

The mainstay of treatment for nephrolithiasis is medical therapy. Surgery is usually reserved for patients with either persistent and severe pain, renal failure, kidney infection and when stone fails to pass or move after 30 days. The surgeries which are being used currently include extracorporeal shockwave lithotripsyureteroscopy and percutaneous nephrolithotomy.

Primary Prevention

Effective measures for the primary prevention of nephrolithiais include diet control and high fluid intake.

Secondary Prevention

Effective measures for the secondary prevention of nephrolithiasis include measures to prevent recurrence of the stones and prevent complications. It includes measures like correcting hydration and dietary habits. Drugs like allopurinol to prevent hyperuricemiapotassium citrate to alkalinize the urine and avoidance or judicious use of diuretics.

References


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