Kidney Stones: Treatment and Prevention

Leonardo Ferreira Fontenelle, MD, MPH, PhD
Thiago Dias Sarti, MD, MPH, PhD

American Family Physician. 2019;99(8):490-496.

Author disclosure: No relevant financial affiliations.

Kidney stones are a common disorder, with an annual incidence of eight cases per 1,000 adults. During an episode of renal colic, the first priority is to rule out conditions requiring immediate referral to an emergency department, then to alleviate pain, preferably with a nonsteroidal anti-inflammatory drug. The diagnostic workup consists of urinalysis, urine culture, and imaging to confirm the diagnosis and assess for conditions requiring active stone removal, such as urinary infection or a stone larger than 10 mm. Conservative management consists of pain control, medical expulsive therapy with an alpha blocker, and follow-up imaging within 14 days to monitor stone position and assess for hydronephrosis. Asymptomatic kidney stones should be followed with serial imaging, and should be removed in case of growth, symptoms, urinary obstruction, recurrent infections, or lack of access to health care. All patients with kidney stones should be screened for risk of stone recurrence with medical history, basic laboratory evaluation, and imaging. Lifestyle modifications such as increased fluid intake should be recommended for all patients, and thiazide diuretics, allopurinol, or citrates should be prescribed for patients with recurrent calcium stones. Patients at high risk of stone recurrence should be referred for additional metabolic assessment, which can serve as a basis for tailored preventive measures.

The prevalence of nephrolithiasis (kidney stones) is increasing in the United States, from one in 20 adults in 1994 to one in 11 adults in 2010.1,2 Worldwide, it is also increasing in Europe and is even higher in the hot-climate “stone belt” extending from the southeastern United States to northern Australia.3,4 Table 1 lists the incidence of different types of kidney stones among children and adults in developed countries.38 Most are of noninfectious etiology and are associated with low fluid intake, hot climate, and certain comorbidities and risk factors (e.g., hypertension; gout; obesity; nonalcoholic fatty liver disease; excessive intake of protein, carbohydrates, and sodium).1,4,911 Increasing exposure to these risk factors may explain the rising incidence of kidney stones and their prevalence in men, non-Hispanic whites, and persons with low socioeconomic status.1,3,4,9 The annual incidence of kidney stones is about eight cases per 1,000 adults and peaks around midlife in developed countries.3

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendation Evidence rating References Comments
Nonsteroidal anti-inflammatory drugs are the first choice for pain relief in patients with kidney stones. A 5, 13, 16, 17 Recommendation from consensus guideline based on meta-analysis of randomized controlled trials
Alpha blockers are the first choice for medical expulsive therapy in patients with kidney stones. A 5, 27 Recommendation from consensus guideline based on meta-analysis of randomized controlled trials
Increasing fluid intake does not relieve pain or accelerate passage of kidney stones. B 19 One randomized controlled trial for each outcome
Patients at low risk of stone recurrence should not routinely undergo extensive metabolic evaluation. C 15, 31, 38 Recommendation from consensus guidelines
Patients should increase daily fluid intake to 2.5 to 3 L per day to prevent recurrence of kidney stones. A 15, 31, 3840 Recommendation from consensus guideline based on meta-analysis of randomized controlled trials
Thiazide diuretics, potassium citrate, or allopurinol should be prescribed after recurrence of calcium stones, even in the absence of metabolic abnormalities. A 15, 31, 38, 39, 41 Recommendation from consensus guideline based on meta-analysis of randomized controlled trials

A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to https://www.aafp.org/afpsort.

BEST PRACTICES IN UROLOGY

Recommendations from the Choosing Wisely Campaign
RecommendationSponsoring organization
Avoid ordering computed tomography of the abdomen and pelvis in young (younger than 50 years), otherwise healthy emergency department patients with histories of kidney stones or ureterolithiasis who present with symptoms consistent with uncomplicated renal colic.American College of Emergency Physicians

Source: For more information on the Choosing Wisely Campaign, see https://www.choosingwisely.org. For supporting citations and to search Choosing Wisely recommendations relevant to primary care, see https://www.aafp.org/afp/recommendations/search.htm.

TABLE 1. Composition of Kidney Stones in Developed Countries

Stone typeChildren (%)Adults (%)
Calcium50 to 9064 to 92
Calcium oxalate60 to 9032 to 46
Calcium phosphate10 to 203 to 5
Both29 to 40
Cystine1 to 51
Struvite (magnesium ammonium phosphate)1 to 182 to 15
Uric acid1 to 103 to 16
Other41

Information from references 3 through 8.

Diagnosis and Acute Management

CLINICAL PRESENTATION

Acute renal colic presents as cramping and intermittent abdominal and flank pain as kidney stones travel down the ureter from the kidney to the bladder.2 Pain is often accompanied by nausea, vomiting, and malaise; fever and chills may also be present.2 Similarity with a previous episode should increase confidence in the diagnosis, although the value of personal or family history during an episode of renal colic is not known. The physical examination should be directed toward excluding differential diagnoses (e.g., urinary tract infection, musculoskeletal inflammation or spasm, ectopic pregnancy, testicular torsion, malignancy; Table 2).2,1214 The initial workup of a patient with suspected kidney stones in the primary care setting should include point-of-care urinalysis to detect blood, because hematuria helps confirm the diagnosis2,5,13,15 (Figure 1).

TABLE 2. Differential Diagnosis of Kidney Stones

Clinical cluesSuggested diagnoses
DysuriaInterstitial cystitis (pelvic pain syndrome), prostatitis, urinary tract infection, vaginitis
Fever, chillsNonspecific response to infection or inflammation (e.g., pyelonephritis)
HematuriaBenign prostatic hyperplasia, renal glomerular disease, urinary tract infection, uroepithelial or prostatic tumor
Nausea, vomitingGastrointestinal disease, intestinal or urinary obstruction, nonspecific response to pain
Pain and tenderness
  • Abdominal

Acute mesenteric ischemia, cholecystitis, gastrointestinal disease, leaking abdominal aortic aneurysm
  • Flank

Dysmenorrhea, herpes zoster, musculoskeletal inflammation or spasm, pyelonephritis, referred pain from gallbladder (on right side), rupture or torsion of ovarian cyst
  • Groin or pelvis

Ectopic pregnancy, hernia, ovarian pathology, pelvic inflammatory disease, pelvic pain syndrome, prostatitis, testicular mass, testicular torsion, urethritis, vaginitis
  • Suprapubic

Interstitial cystitis, peritonitis, prostatitis, urinary calculi, urinary tract infection
Urinary frequencyBenign prostatic hyperplasia, bladder spasms, high fluid intake, hyperglycemia, urinary tract infection

Adapted with permission from Frassetto L, Kohlstadt I. Treatment and prevention of kidney stones: an update. Am Fam Physician. 2011;84(11):1235, with additional information from references 12 through 14.

FIGURE 1.

Algorithm for the diagnosis and management of acute kidney stones.

ACUTE MANAGEMENT

Pain relief is the priority in the acute management of renal colic.5,13 Nonsteroidal anti-inflammatory drugs (e.g., ketorolac, 30 to 60 mg intramuscularly) are more effective and have fewer adverse effects than opioids.5,13,16,17 If an opioid is used, meperidine (Demerol) should be avoided because of the significant risk of nausea and vomiting.17,18 Neither scopolamine nor increased fluid intake alleviates renal colic.16,19

Immediate referral to a urologist or emergency department is warranted when medical analgesia is insufficient; when sepsis is suspected; when anuria, bilateral obstruction, urinary tract infection with renal obstruction, or obstruction of the sole functioning kidney are present; in women who are pregnant or have delayed menstruation (because of the risk of ectopic pregnancy); and in patients who have potential comorbidities or are older than 60 years, especially those with arteriopathy (because of the risk of leaking abdominal aortic aneurysm).5,13,14

DIAGNOSTIC WORKUP

When immediate referral is not indicated, urine culture and urinalysis (if not already done) should be ordered to rule out infection, as well as imaging to confirm the diagnosis of kidney stones and assess for hydronephrosis and stone size and position.2,5,13,15 Although non–contrast-enhanced computed tomography (CT) of the abdomen and pelvis has superior sensitivity and specificity and is commonly performed in the emergency department,5,2022 first-line ultrasonography has acceptable performance and is more cost-effective.5,13,20 Intravenous urography with plain radiography has limited accuracy and is no longer the preferred diagnostic imaging modality for kidney stones.5 There is no direct evidence for the optimal timing of diagnostic workup for acute renal colic in the primary care setting. However, a 2002 evidence-based consensus review from the United Kingdom recommended that ultrasonography be performed within one week of symptom onset.13 Referral to a urologist for active stone removal is warranted when the stone is larger than 10 mm or if significant hydronephrosis is present.5,13

FOLLOW-UP

Conservative management is indicated if referral is not necessary. Patients should receive pain medication as needed, and follow-up imaging (ultrasonography and possibly plain radiography) should be obtained once within 14 days to monitor evolving stone position and assess for hydronephrosis.5,23 Complete urinary obstruction causes irreversible loss of kidney function, but patients with well-controlled pain and no significant degree of hydronephrosis have only partial obstruction and can be followed for about four to six weeks.5,13,2326 If the stone does not pass spontaneously, the patient should be referred to a urologist for active stone removal.

Approximately 86% of kidney stones pass spontaneously; this proportion is lower for stones larger than 6 mm (59% vs. 90% for smaller stones).24 Although stones larger than 6 mm in diameter are often removed by urologists,5 these are the stones that have greatest benefit from medical expulsive therapy.27 Medical expulsive therapy with alpha blockers (e.g., tamsulosin [Flomax], 0.4 mg per day; doxazosin [Cardura], 4 mg per day) hastens and increases the likelihood of stone passage, reduces pain, and prevents surgical interventions and hospital admissions.5,27 These medications should be offered to patients with distal ureteral stones 5 to 10 mm in diameter.27 Tamsulosin is the most studied medication, but other alpha blockers seem equally effective.27 Calcium channel blockers (e.g., nifedipine) are less effective and may be no more effective than placebo.2830 Coadministration of oral corticosteroids or increasing fluid intake does not hasten stone passage or alleviate renal colic.5,19

Further Evaluation in the Subacute Setting

Patients with newly diagnosed kidney stones should receive a basic evaluation consisting of a detailed medical history, serum chemistry, and urinalysis/urine culture. Patients at risk of stone recurrence (Table 331 and Table 42,3235 ) should be referred for additional metabolic testing (e.g., 24-hour urine collection for total volume, pH, and calcium oxalate, uric acid, citrate, sodium, potassium, and creatinine levels) and individualized preventive measures.15,31 The medical history should review the stone history (including family history of kidney stones), diet, current medications, and conditions associated with an increased risk of kidney stones.2,15,3134

TABLE 3. Risk Factors for Kidney Stone Recurrence

  • Anatomic abnormalities

  • Calyceal diverticulum or cyst

  • Horseshoe kidney

  • Medullary sponge kidney (tubular ectasia)

  • Ureteral stricture

  • Ureterocele

  • Ureteropelvic junction obstruction

  • Vesicoureteral reflux

  • Diseases

  • Gastrointestinal diseases and bariatric surgery (e.g., Crohn disease, enteric hyperoxaluria after urinary diversion, intestinal resection, jejunoileal bypass, malabsorptive conditions)

  • Hyperparathyroidism

  • Nephrocalcinosis

  • Sarcoidosis

  • General factors

  • Calcium phosphate stones

  • Early onset of urolithiasis (especially children and teenagers)

  • Family history of stone formation

  • Infection-associated stones (struvite or carbonate apatite stones)

  • Solitary kidney*

  • Uric acid– and urate-containing stones

  • Genetic factors

  • 2,8-dihydroxyadenine

  • Cystic fibrosis

  • Cystinuria (types A, B, and AB)

  • Lesch-Nyhan syndrome

  • Primary hyperoxaluria

  • Renal tubular acidosis type I

  • Xanthinuria

  • Medication use (Table 4)

*—The solitary kidney itself does not particularly increase the risk of stone formation, but prevention of stone recurrence is of more importance.

Adapted with permission from Skolarikos A, Straub M, Knoll T, et al. Metabolic evaluation and recurrence prevention for urinary stone patients: EAU guidelines. Eur Urol. 2015;67(4):752.

TABLE 4. Medications Associated with Kidney Stone Formation

Type of medicationExamples
AntibioticsAmpicillin, amoxicillin, ceftriaxone (Rocephin), furans (e.g., nitrofurantoin), pyridines, quinolones, sulfonamides (e.g., sulfamethoxazole)
Carbonic anhydrase inhibitorsAcetazolamide, topiramate (Topamax)
DiureticsFurosemide (Lasix), triamterene (Dyrenium)
Ephedra alkaloids (banned in the United States)Herbal products used as stimulants and appetite suppressants
Laxatives, especially if abused (specific to ammonium urate stones)Overuse of any laxative resulting in electrolyte losses
Potassium channel blockersAmiodarone, dalfampridine (Ampyra; multiple sclerosis therapy), sotalol (Betapace)
Reverse transcriptase inhibitors and protease inhibitorsEfavirenz (Sustiva), indinavir (Crixivan), nelfinavir (Viracept), raltegravir (Isentress)
SulfonylureasTherapies for type 2 diabetes mellitus
OthersAluminum magnesium hydroxide, ascorbic acid, calcium, dexamethasone, guaifenesin, phenytoin (Dilantin), vitamin D

Adapted with permission from Frassetto L, Kohlstadt I. Treatment and prevention of kidney stones: an update. Am Fam Physician. 2011;84(11):1237, with additional information from references 32 through 35.

The patient should be instructed to strain his or her urine to catch the stone, then send the stone in a urine specimen cup or a clean, dry container for analysis; non–calcium oxalate stones require additional metabolic testing.15,31 Recurrent stones should also be considered for analysis because their composition may differ from the initial stone.15,31 When stone analysis is not available, ultrasonography should be ordered to look for renal abnormalities if it was not performed before the stone was passed. Non–contrast-enhanced CT should be considered if residual stone is suspected; this modality may help identify stone composition.31

Basic laboratory evaluations include creatinine (for renal function), ionized calcium (for hyperparathyroidism), and uric acid (for hyperuricemia); parathyroid hormone should be measured only if the serum calcium level is high.15,31 If a stone was not retrieved for analysis, additional tests should be considered: urine pH (for nephrocalcinosis and other metabolic abnormalities), microscopy of sediment from morning urine (for urine crystals that may suggest stone composition), and a test for cystinuria (especially in children because it is an inherited metabolic disorder).31

Special Considerations

ASYMPTOMATIC KIDNEY STONES

Many kidney stones are asymptomatic and found on imaging; each year, 10% to 25% become symptomatic or require intervention.5 Conservative management is an option for adults who are healthy, unfit for surgery, or pregnant, and who have access to health care and can adhere to active surveillance (imaging after six months, then annually).5,36 The patient should be referred for stone removal if symptoms, obstruction, or recurrent infection develops, or if the stone grows larger.5,36 Stone removal should be considered if the patient prefers removal to conservative management; plans to conceive in the near future; has calyceal diverticular stones, stones larger than 10 mm (possibly larger than 4 mm), or renal pathology; or is unsuited for conservative management.36

CHILDREN

Kidney stones are becoming more prevalent in children because of increasing rates of diabetes mellitus, obesity, and hypertension in this population.24,9 Increasing age is a risk factor for kidney stones; therefore, adolescents are more likely to form stones than younger children.2 Children with kidney stones are more likely to have a metabolic, neurologic, or congenital urinary system structural abnormality; to have concomitant urinary infection; and to have recurrent stones.2,3,9,31

PREGNANT WOMEN

Urinary stasis, increased glomerular filtration rate, and elevated urine pH affect kidney stone formation in pregnant women. Up to 75% of stones in pregnant women are composed of calcium phosphate, in contrast with other adults, in whom calcium oxalate stones are most common.5 Diagnostic and treatment options are limited during pregnancy because of risk to the fetus.5 Kidney stones may increase the risk of preterm labor and other maternal and fetal complications.37

Prevention

Measures to prevent recurrence of kidney stones include lifestyle modifications, citrate supplementation, and medications.2,15,31,38,39 Lifestyle modifications are the cornerstone of prevention after a first kidney stone in patients with low risk of recurrence, whereas citrate supplementation and medications are reserved for patients with recurrent stones.15,31,38,39 Patients at high risk of stone recurrence should receive preventive measures tailored to the results of the metabolic assessment.

LIFESTYLE MODIFICATIONS

The most important lifestyle modification to prevent recurrent kidney stones is to increase fluid intake to 2.5 to 3 L per day to guarantee diuresis of 2 to 2.5 L per day and a urine specific gravity lower than 1.010.15,31,3840 Fluids should be consumed throughout the day and should consist of beverages with a neutral pH.31 Collection of urine over 24 hours may be necessary to ensure that the diuresis target is met. Decreasing intake of carbonated drinks, especially those acidified with phosphoric acid (e.g., colas), further reduces risk of stone recurrence.38,39

Overall, a balanced diet is ideal for preventing stone recurrence.15,31 The diet should be high in fiber and vegetables, with normal calcium content (1.0 to 1.2 g per day) and limited sodium (4 to 5 g per day) and animal protein (0.8 to 1.0 g per kg per day).15,31 Patients who are obese or over-weight should pursue a normal body weight through dietary modification and increased physical activity.2,15,31 Although there is limited evidence to support lifestyle modifications for the prevention of kidney stone recurrence, these changes are important for preventing comorbidities.

CITRATE SUPPLEMENTATION AND MEDICATIONS

Thiazide diuretics, allopurinol, and citrate supplementation are effective in preventing calcium stones that recur despite lifestyle modification, even in the absence of hyperuricemia, urinary acidosis, hypocitraturia, or hyperuricosuria.15,31,38,39,41 The effectiveness of thiazide diuretics has been documented only with high dosages (e.g., hydrochlorothiazide, 50 mg per day; chlorthalidone, 25 to 50 mg per day; indapamide, 2.5 mg per day); lower dosages have fewer adverse effects, but their effectiveness is unknown.38,39

Allopurinol should be started at 100 mg once per day and increased gradually to 100 mg three times per day.31 There is no evidence that combination therapy with thiazide diuretics or alkaline citrates is more effective than monotherapy.15,31,38,39 Allopurinol is one of the mainstays of therapy for patients with calcium stones, but most patients with uric acid stones have acidic urine that requires treatment with alkaline citrates.15,31

Citrate supplementation is used not only for calcium stones, but also for uric acid (urine pH target 6.0 to 7.5 or greater) and cystine stones (urine pH target of 7.0 to 7.5 or greater).15,31 The preferred salt for supplementation is potassium citrate at a target dosage of 5 to 12 g per day.15,31,38,41 The initial dosage should be 9 g per day, divided into three doses and taken within 30 minutes of meals or a bedtime snack. The most common adverse effects are gastrointestinal symptoms. Potassium citrate supplementation may correct low serum potassium levels caused by thiazide diuretics, but there is no evidence that combination therapy is more effective than monotherapy with either agent.15,31,38,39 Sodium citrate is an alternative for citrate supplementation, but the resulting excretion of sodium and calcium may partially counteract the intended effect.15,31,38 Unsweetened lemonade is a more palatable and less expensive alternative for citrate supplementation. Although there is no direct evidence of its effectiveness in preventing stone recurrence, the dilution of lemon juice in water should help patients meet the recommended fluid intake.42

If medication or citrate supplementation is prescribed, serum potassium levels (for patients taking thiazide diuretics or potassium citrate) and liver enzymes (allopurinol) should be monitored to detect potentially serious adverse effects.15 Potassium levels should be monitored before prescription, within two weeks of prescription, and then every 12 months (earlier if illness occurs or another medication is added).43 There are no recommendations on the frequency of monitoring for hepatotoxicity.

This article updates previous articles on this topic by Frassetto and Kohlstadt2; Pietrow and Karellas12; Goldfarb and Coe44; and Portis and Sundaram.45

Data Sources: We searched PubMed (using PubMed Clinical Queries, ACCESSSS, and Essential Evidence Plus), LILACS (using Virtual Health Library), Essential Evidence, and the Cochrane Database of Systematic Reviews (through PubMed, LILACS, Essential Evidence Plus, and the Cochrane Library) using the key terms kidney calculi, ureterolithiasis, urinary calculi, urolithiasis, or nephrolithiasis. Search dates: November 2017 to December 2018.

LEONARDO FERREIRA FONTENELLE, MD, MPH, PhD, is a professor at Universidade Vila Velha Medical School, Vila Velha, Espírito Santo, Brazil.

THIAGO DIAS SARTI, MD, MPH, PhD, is a professor in the Department of Social Medicine at the Health Sciences Center of Universidade Federal do Espírito Santo, Vitória.

Address correspondence to Leonardo Ferreira Fontenelle, MD, MPH, PhD, Universidade Vila Velha, Rua Sao Joao, No. 48, Vila Velha, Espírito Santo, Brazil 29101-420 (e-mail: leonardof@leonardof.med.br). Reprints are not available from the authors.

Author disclosure: No relevant financial affiliations.

  1. 1.Scales CD, Smith AC, Hanley JM, Saigal CS Urologic Diseases in America Project. Prevalence of kidney stones in the United States. Eur Urol. 2012;62(1):160-165.
  2. 2.Frassetto L, Kohlstadt I. Treatment and prevention of kidney stones: an update. Am Fam Physician. 2011;84(11):1234-1242.
  3. 3.Alatab S, Pourmand G, El Howairis Mel F, et al. National profiles of urinary calculi: a comparison between developing and developed worlds. Iran J Kidney Dis. 2016;10(2):51-61.
  4. 4.López M, Hoppe B. History, epidemiology and regional diversities of urolithiasis. Pediatr Nephrol. 2010;25(1):49-59.
  5. 5.Türk C, Petřík A, Sarica K, et al. EAU guidelines on diagnosis and conservative management of urolithiasis. Eur Urol. 2016;69(3):468-474.
  6. 6.Sharma AP, Filler G. Epidemiology of pediatric urolithiasis. Indian J Urol. 2010;26(4):516-522.
  7. 7.Gabrielsen JS, Laciak RJ, Frank EL, et al. Pediatric urinary stone composition in the United States. J Urol. 2012;187(6):2182-2187.
  8. 8.Alelign T, Petros B. Kidney stone disease: an update on current concepts. Adv Urol. 2018;2018:3068365.
  9. 9.Roudakova K, Monga M. The evolving epidemiology of stone disease. Indian J Urol. 2014;30(1):44-48.
  10. 10.Aune D, Mahamat-Saleh Y, Norat T, Riboli E. Body fatness, diabetes, physical activity and risk of kidney stones: a systematic review and meta-analysis of cohort studies. Eur J Epidemiol. 2018;33(11):1033-1047.
  11. 11.Wijarnpreecha K, Lou S, Panjawatanan P, et al. Nonalcoholic fatty liver disease and urolithiasis. A systematic review and meta-analysis. J Gastrointestin Liver Dis. 2018;27(4):427-432.
  12. 12.Pietrow PK, Karellas ME. Medical management of common urinary calculi. Am Fam Physician. 2006;74(1):86-94.
  13. 13.Wright PJ, English PJ, Hungin AP, Marsden SN. Managing acute renal colic across the primary-secondary care interface: a pathway of care based on evidence and consensus [published correction appears in BMJ. 2003;326(7379):18]. BMJ. 2002;325(7377):1408-1412.
  14. 14.Bultitude M, Rees J. Management of renal colic. BMJ. 2012;345:e5499.
  15. 15.Pearle MS, Goldfarb DS, Assimos DG, et al. Medical management of kidney stones: AUA guideline. J Urol. 2014;192(2):316-324.
  16. 16.Afshar K, Jafari S, Marks AJ, Eftekhari A, MacNeily AE. Nonsteroidal anti-inflammatory drugs (NSAIDs) and non-opioids for acute renal colic. Cochrane Database Syst Rev. ;2015(6):CD006027.
  17. 17.Holdgate A, Pollock T. Systematic review of the relative efficacy of non-steroidal anti-inflammatory drugs and opioids in the treatment of acute renal colic [published correction appears in BMJ. 2004;329(7473):1019]. BMJ. 2004;328(7453):1401.
  18. 18.Pathan SA, Mitra B, Cameron PA. A systematic review and meta-analysis comparing the efficacy of nonsteroidal anti-inflammatory drugs, opioids, and paracetamol in the treatment of acute renal colic. Eur Urol. 2018;73(4):583-595.
  19. 19.Worster AS, Bhanich Supapol W. Fluids and diuretics for acute ureteric colic. Cochrane Database Syst Rev. ;2012(2):CD004926.
  20. 20.Smith-Bindman R, Aubin C, Bailitz J, et al. Ultrasonography versus computed tomography for suspected nephrolithiasis. N Engl J Med. 2014;371(12):1100-1110.
  21. 21.Niemann T, Kollmann T, Bongartz G. Diagnostic performance of low-dose CT for the detection of urolithiasis: a meta-analysis. AJR Am J Roentgenol. 2008;191(2):396-401.
  22. 22.Rodger F, Roditi G, Aboumarzouk OM. Diagnostic accuracy of low and ultra-low dose CT for identification of urinary tract stones: a systematic review. Urol Int. 2018;100(4):375-385.
  23. 23.Fulgham PF, Assimos DG, Pearle MS, Preminger GM. Clinical effectiveness protocols for imaging in the management of ureteral calculous disease: AUA technology assessment. J Urol. 2013;189(4):1203-1213.
  24. 24.Tchey DU, Ha YS, Kim WT, Yun SJ, Lee SC, Kim WJ. Expectant management of ureter stones: outcome and clinical factors of spontaneous passage in a single institution's experience. Korean J Urol. 2011;52(12):847-851.
  25. 25.Ahmed AF, Gabr AH, Emara AA, Ali M, Abdel-Aziz AS, Alshahrani S. Factors predicting the spontaneous passage of a ureteric calculus of ≥ 10 mm. Arab J Urol. 2015;13(2):84-90.
  26. 26.Coll DM, Varanelli MJ, Smith RC. Relationship of spontaneous passage of ureteral calculi to stone size and location as revealed by unenhanced helical CT. AJR Am J Roentgenol. 2002;178(1):101-103.
  27. 27.Hollingsworth JM, Canales BK, Rogers MA, et al. Alpha blockers for treatment of ureteric stones: systematic review and meta-analysis. BMJ. 2016;355:i6112.
  28. 28.Wang H, Man LB, Huang GL, Li GZ, Wang JW. Comparative efficacy of tamsulosin versus nifedipine for distal ureteral calculi: a meta-analysis. Drug Des Devel Ther. 2016;10:1257-1265.
  29. 29.Pickard R, Starr K, MacLennan G, et al. Medical expulsive therapy in adults with ureteric colic: a multicentre, randomised, placebo-controlled trial. Lancet. 2015;386(9991):341-349.
  30. 30.Chua ME, Park JH, Castillo JC, Morales ML. Terpene compound drug as medical expulsive therapy for ureterolithiasis: a meta-analysis. Urolithiasis. 2013;41(2):143-151.
  31. 31.Skolarikos A, Straub M, Knoll T, et al. Metabolic evaluation and recurrence prevention for urinary stone patients: EAU guidelines. Eur Urol. 2015;67(4):750-763.
  32. 32.Daudon M, Frochot V, Bazin D, Jungers P. Drug-induced kidney stones and crystalline nephropathy: pathophysiology, prevention and treatment. Drugs. 2018;78(2):163-201.
  33. 33.Bjelakovic G, Gluud LL, Nikolova D, et al. Vitamin D supplementation for prevention of mortality in adults. Cochrane Database Syst Rev. 2014(1):CD007470.
  34. 34.Izzedine H, Lescure FX, Bonnet F. HIV medication-based urolithiasis. Clin Kidney J. 2014;7(2):121-126.
  35. 35.Kahwati LC, Weber RP, Pan H, et al. Vitamin D, calcium, or combined supplementation for the primary prevention of fractures in community-dwelling adults: evidence report and systematic review for the US Preventive Services Task Force. JAMA. 2018;319(15):1600-1612.
  36. 36.Streeper NM. Asymptomatic renal stones—to treat or not to treat. Curr Urol Rep. 2018;19(5):29.
  37. 37.Semins MJ, Matlaga BR. Management of urolithiasis in pregnancy. Int J Womens Health. 2013;5:599-604.
  38. 38.Qaseem A, Dallas P, Forciea MA, Starkey M, Denberg TD. Dietary and pharmacologic management to prevent recurrent nephrolithiasis in adults: a clinical practice guideline from the American College of Physicians. Ann Intern Med. 2014;161(9):659-667.
  39. 39.Fink HA, Wilt TJ, Eidman KE, et al. Medical management to prevent recurrent nephrolithiasis in adults: a systematic review for an American College of Physicians clinical guideline [published correction appears in Ann Intern Med. 2013;159(3):230-232]. Ann Intern Med. 2013;158(7):535-543.
  40. 40.Fink HA, Akornor JW, Garimella PS, et al. Diet, fluid, or supplements for secondary prevention of nephrolithiasis: a systematic review and meta-analysis of randomized trials. Eur Urol. 2009;56(1):72-80.
  41. 41.Phillips R, Hanchanale VS, Myatt A, Somani B, Nabi G, Biyani CS. Citrate salts for preventing and treating calcium containing kidney stones in adults. Cochrane Database Syst Rev. ;2015(10):CD010057.
  42. 42.Prezioso D, Strazzullo P, Lotti T, et al. Dietary treatment of urinary risk factors for renal stone formation. A review of CLU Working Group [published correction appears in Arch Ital Urol Androl. 2016;88(1):76]. Arch Ital Urol Androl. 2015;87(2):105-120.
  43. 43.McDowell SE, Thomas SK, Coleman JJ, Aronson JK, Ferner RE. A practical guide to monitoring for adverse drug reactions during antihypertensive drug therapy [published correction appears in J R Soc Med. 2013;106(4):119]. J R Soc Med. 2013;106(3):87-95.
  44. 44.Goldfarb DS, Coe RL. Prevention of recurrent nephrolithiasis. Am Fam Physician. 1999;60(8):2269-2276.
  45. 45.Portis AJ, Sundaram CP. Diagnosis and initial management of kidney stones. Am Fam Physician. 2001;63(7):1329-1339.

Copyright © 2026 by the American Academy of Family Physicians.

This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP. See permissions for copyright questions and/or permission requests.